Archive for March, 2009

Chevrolet 90-Degree V6 engine

Thursday, March 26th, 2009

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Chevrolet 90� V6 engine

Manufacturer
General Motors

Type
90� OHV V6

Production
1978�

Bore
3.50 in3.736 in4.00 in

Stroke
3.48 in

Displacement
200cid (3.3L)229cid (3.8L)262cid (4.3L)

Block alloy
Iron

Head alloy
Iron

Valvetrain
OHV
The Chevrolet 90� V6 family of engines began in 1978 with the Chevrolet 200cid (3.3L) V6 as the base engine for the all new 1978 Chevrolet Malibu. This engine family is still produced today, as the 4.3L V6 engine used in Chevrolet trucks and vans.
These engines have a 90� vee block with 12 valves activated by a pushrod valvetrain. All engines have cast iron blocks and cylinder heads. The engines are based on the Chevrolet Small-Block engine, and the V6 is formed by the removal of the #3 and #6 cylinders. The V6s share the same 4.4" bore spacing and 9.025" deck height as the V8 engines. Many parts are interchangeable between the 90� V6 and the small block V8 including valvetrain components, bearings, piston assemblies, lubrication and cooling system components, and external accessories. [1] The 90-degree V6 engine uses the same transmission bellhousing pattern as the Chevrolet small-block V8 engine. All the engines use a 1-6-5-4-3-2 firing order.[2] The engines in this family are longitudinal engines, and have only been used in rear-wheel drive cars and trucks.

Contents

1 3.3L (200 CID)
2 3.8L (229 CID)
3 4.3L (262 CID) 

3.1 LB1 and LB4
3.2 LU2
3.3 L35 CPI
3.4 L35 and LF6 SCPI
3.5 LU3 and LG3 MPFI
3.6 Turbocharged LB4 4.3L V6
4 Notes
5 References 

//

 3.3L (200 CID)
Introduced in 1978, the 200cid replaced the larger 250cid as the base engine for Chevrolet's new downsized intermediate line. The 200cid used a unique 3.5" bore and a 3.48" stroke similar to the Chevrolet 305cid and 350cid V8 engines. These bore and stroke dimensions were later used by the 267cid V8 Cheverolet engine. Also like the small block V8 engines, the 200cid V6 used 2.45" main bearings and 2.10" rod bearing diameters.
Being a 90-degree V6, Chevrolet took steps to eliminate the rough running tendencies of the 200. The crankshaft has each of its connecting rod throws offset by 18 degrees for each pair of rods. This required the connecting rods to have 0.050" narrower ends as well as a thrust bearing to be installed between each pair of rods. However, the connecting rods were still the same 5.7" in length as most other small block Chevrolet V8 engines. This produced an engine that with a semi-even fire sequence of 132 deg./108 degrees. [2]
The 200cid V6 was only produced for 1978 and 1979. It was only ever available with a 2-barrel carburetor. In 1978, the 200cid used the Rochester 2GC carburetor and in 1979 it used a Rochester Dualjet carburetor. The smaller carburetor caused a slight decrease in power.

Year
Horsepower
Torque
Bore and Stroke
Carburetor
Compression Ratio

1978
95hp (71kW) @ 3800 rpm
160lb穎t (217N穖) @2000 rpm
3.50" x 3.48"
2-BBL 2GC
8.20:1

1979
94hp (70kW) @ 4000 rpm
154lb穎t (209N穖) @2000 rpm
3.50" x 3.48"
2-BBL M2ME
8.20:1

 3.8L (229 CID)
The 229cid engine was first introduced for the 1980 model year and was produced until 1984. This engine replaced the 250cid in fullsize Chevrolets and Camaros as the new base V6. Additionally, the intermediate Chevrolet Malibu and Monte Carlo also used the 229cid as a replacement for both the 200cid V6, and the 231cid Buick V6. Both the 231cid Buick V6 and the 229cid Chevrolet V6 are 90 degree V6 engines, and both are often referred to as the 3.8L V6. These engines should not be confused as being the same, and are completely unique engine designs.
The 229cid has a 3.736" bore and a 3.48" stoke, identical to the Chevrolet 305cid V8 engine. The 229cid used the same 2.45" main bearing and 2.10" rod bearing diameters as the 200cid V6 engine. Also like the 200cid V6, the 229cid used the same crankshaft with the 18 degree offset throws and the same 5.7" connecting rods with 0.050" narrowed ends. It came equipped with 1.84" intake valves and 1.50" exhaust valves. The 229cid V6 was only equipped with a 2-barrel carburetor. For 1980 the 229cid used a mechanical Dualjet. From 1981 - 1984 the electronic Dualjet was used along with the GM's CCC (Computer Command Control) system. The 229cid was rated between 110 and 115hp (86kW).

Year
Horsepower
Torque
Bore and Stroke
Carburetor
Compression Ratio

1980
115hp (86kW) @ 4000 rpm
175lb穎t (237N穖) @ 2000 RPM
3.736" x 3.48"
2-BBL M2ME
8.60:1

1981-82
110hp (82kW) @ 4200 rpm
170lb穎t (230N穖) @ 2000 RPM
3.736" x 3.48"
2-BBL E2ME
8.60:1

1983-84
110hp (82kW) @ 4000 rpm
190lb穎t (258N穖) @ 1600 RPM
3.736" x 3.48"
2-BBL E2ME
8.60:1

 4.3L (262 CID)
The 4.3L (262cid) V6 is the last and most successful engine in the Chevrolet 90-degree V6 engine family. This engine was introduced in 1985 as a replacement for the 229cid V6 in the fullsize Chevrolet and the Chevrolet El Camino. It also replaced the 250cid in the Chevrolet fullsize trucks and fullsize vans as the new base six cylinder engine.
The 4.3L V6 has a 4.00" bore and a 3.48" stroke, identical to the 350cid Chevrolet V8 engine. To create a true even fire engine, Chevrolet produced a crankshaft with 30 degree offsets between each rod pin. Consequentially, rod journals were increased to a larger 2.25". The connecting rods used on the 4.3L are therefore unique to this engine, being 5.7" in length, but having the larger 2.25" journals. The 4.3L also used larger valves than the 229cid V6, with a 1.94" intake valve and a 1.50" exhaust valve. [2]
In 1986 and 1987, the 4.3L engine saw engine design upgrades similar to the Chevrolet small block V8. In 1986, the rear main crankshaft oil seal was changed from a two piece to a once piece seal. Some 1985 model year vehicles would have a 1986 engine due to service replacement - cylinder blocks were shipped with oil pans. [3]1987 saw new center bolt valve covers and hydraulic roller lifters. [4]
For the 1992 model year, the 4.3L had its block design modified to allow a balance shaft to be installed. [5] Even though the 4.3L is an even fire V6, the 90 degree block layout is not ideal for smoothness. The balance shaft on the 4.3L is installed above the top timing gear, and runs through the top of the lifter valley. It is gear driven off the timing chain, and therefore a new timing chain cover was designed for these balanced 4.3L V6s.

 LB1 and LB4
In 1985, the 4.3L was either equipped with throttle-body fuel injection, RPO LB4 or a Rochester Quadrajet 4-Barrel carburetor, RPO LB1. The Chevrolet fullsize sedans and the Chevrolet El Camino used the LB4 rated at 130hp (97kW). Pick-ups and Vans used the LB1 version rated at 155hp (116kW). The LB1 used in trucks and vans was referred to as Vortec in Chevrolet literature, and this name continued to be used with all truck and van 4.3L V6s until present day.
In 1986, the 4.3L engine used in the Chevrolet Caprice and El Camino saw an increase in power to 140hp (100kW). This engine remained unchanged until 1990 when it was last used in taxi and Police Chevrolet Caprices. In 1986 the Chevrolet Astro and GMC Safari vans used the fuel injected LB4 instead of the LB1. In 1987, the Chevrolet full size pick-ups and fullsize vans were upgraded to use the LB4 throttle-body injection version of the 4.3L. From 1987 onwards LB4s output was 160hp (120kW) for pickups, while fullsize vans were rated at 150hp (110kW). In 1988 the S-series trucks and S-Blazer and Jimmys had the LB4 4.3L as an available option (the accessory drive was upgraded to a serpentine belt drive). The LB4 continued until 1996 with minor variations in power, but without any major change.

Year
Horsepower
Torque
Fuel System
Compression Ratio
RPO
Applications

1985-86
155hp (116kW) @ 4000 rpm
230lb穎t (312N穖) @ 2400 RPM
4-BBL
9.3:1
LB1
1,2,3

1985
130hp (97kW) @ 3600 rpm
210lb穎t (285N穖) @ 2000 RPM
TBI
9.3:1
LB4
4,5

1986-90
140hp (100kW) @ 4000 rpm
225lb穎t (305N穖) @ 2000 RPM
TBI
9.3:1
LB4
4,5

1987-88
145hp (108kW) @ 4200 rpm
225lb穎t (305N穖) @ 2000 RPM
TBI
9.3:1
LB4
5

1986
160hp (120kW) @ 4000 rpm
235lb穎t (319N穖) @ 2400 RPM
TBI
9.3:1
LB4
3

1987-92
150hp (110kW) @ 4000 rpm
230lb穎t (312N穖) @ 2400 RPM
TBI
9.3:1
LB4
2

1987-92
160hp (120kW) @ 4000 rpm
235lb穎t (319N穖) @ 2400 RPM
TBI
9.1:1
LB4
1,3,6,7

1993-95
155hp (116kW) @ 4000 rpm
230lb穎t (312N穖) @ 2000 RPM
TBI
9.1:1
LB4
2

1993-95
165hp (123kW) @ 4000 rpm
235lb穎t (319N穖) @ 2000 RPM
TBI
9.1:1
LB4
1,3,6,7
Legend

1 - Chevrolet C/K Trucks, GMC C/K Trucks
2 - Chevrolet G-Series Vans, GMC G-Series Vans
3 - Chevrolet Astro vans, GMC Safari Vans - NOTE - LB1 for 1985 only & LB4 not available 1995
4 - 1985 Chevrolet Impala, 1985-1988 Chevrolet Caprice, 1989-90 Chevrolet Caprice Police/Taxi only, 1985-86 Pontiac Parisienne
5 - 1985-88 Chevrolet El Camino, GMC Caballero, Chevrolet Monte Carlo - NOTE - 140 hp LB4 used 1986 only
6 - 1988-94 Chevrolet S-10 Blazer, GMC S-15 Jimmy and 1991 Oldsmobile Bravada
7 - 1988-95 Chevrolet S-10 and GMC S-15 Sonoma 

 LU2
For the 1990-1991 model years a high ouotput 4.3L V6 was an available option for the Chevrolet Astro and GMC Safari vans. The LU2 used unique hypereutectic, strutless pistons and a more aggressive camshaft. Like the LB4, the LU2 used throttle-body fuel injection, but was rated at 170hp (130kW) and 260ftç©•bf (350Nç©–) of torque. This engine was replaced in 1992 with the L35.

Year
Horsepower
Torque
Fuel System
Compression Ratio
RPO
Applications

1990-92
170hp (130kW) @ 4600 rpm
260lb穎t (353N穖) @ 3400 RPM
TBI
9.1:1
LU2
1
Legend

1 - Chevrolet Astro vans, GMC Safari Vans - optional on extended length models 

 L35 CPI
1992 introduced a new version of the 4.3L, the L35. This version of the 4.3L was equipped with CPI (Central Port Fuel Injection). This system had one centrally located fuel injector distribute fuel to six hoses each with a poppet valve to each of the intake ports. This system allowed for a multi-point injection, using one injector. The fuel injection was a batch fire system and used a two piece cast aluminum dual-plenum manifold. This engine was available in S-10 Blazers and S15-Jimmys and Astro and Safari vans only. The L35 was rated at 200hp (150kW) and 260ftç©•bf (350Nç©–) of torque.

Year
Horsepower
Torque
Fuel System
Compression Ratio
RPO
Applications

1992-94
200hp (150kW) @ 4500 rpm
260lb穎t (353N穖) @ 3600 RPM
CPI
9.1:1
L35
1,2,3

1995
190hp (140kW) @ 4500 rpm
260lb穎t (353N穖) @ 3400 RPM
CPI
9.1:1
L35
1

1995
191hp (142kW) @ 4500 rpm
260lb穎t (353N穖) @ 3400 RPM
CPI
9.1:1
L35
3

1995
195hp (145kW) @ 4500 rpm
260lb穎t (353N穖) @ 3400 RPM
CPI
9.1:1
L35
2
Legend

1 - Chevrolet Astro vans, GMC Safari Vans - NOTE std on AWD, opt on 2WD models
2 - Chevrolet S-10 Blazer, GMC Jimmy and Oldsmobile Bravada - NOTE - Oldsmobile Bravada not produced in 1995
3 - Chevrolet S-10 and GMC Sonoma 

 L35 and LF6 SCPI
Major design changes to the 4.3L V6 for the 1996 model year. Like other small block Chevrolet V8s, the 4.3L engine received redesigned heads which had improved airflow and combustion efficiency. These heads are referred to as Vortec heads. Furthermore the 4.3L was upgraded to receive sequential port fuel injection. The fuel system uses six centrally mounted injectors firing into six nylon hoses with poppet valves leading to each intake port. This system was call SCPI (Sequential Central Port Injection). This 4.3L used a two piece manifold, with the upper half manufactured from a composite plastic and the lower half manufactured from cast aluminum.
This engine came in two versions, the LF6 rated at 175hp (130kW) - 180hp (130kW), and the L35 rated at 180 - 200hp (150kW). Only the S-series pick-ups used the LF6, while the fullsize trucks, vans and Blazer and Jimmy used the L35 version. The L35 was optional on the S-Series trucks.

Year
Horsepower
Torque
Fuel System
Compression Ratio
RPO
Applications

1996
170hp (130kW) @ 4400 rpm
235lb穎t (319N穖) @ 2800 RPM
SCPI
9.2:1
LF6
5

1997-2002
175hp (130kW) @ 4400 rpm
240lb穎t (325N穖) @ 2800 RPM
SCPI
9.2:1
LF6
5

1996-2002
180hp (130kW) @ 4400 rpm
240lb穎t (325N穖) @ 2800 RPM
SCPI
9.2:1
LF6
6

1996-2002
180hp (130kW) @ 4400 rpm
245lb穎t (332N穖) @ 2800 RPM
SCPI
9.2:1
L35
5

1996-2002
190hp (140kW) @ 4400 rpm
250lb穎t (339N穖) @ 2800 RPM
SCPI
9.2:1
L35
3,4,6

1996-2002
200hp (150kW) @ 4400 rpm
250lb穎t (339N穖) @ 2800 RPM
SCPI
9.2:1
L35
2

1996-1998
200hp (150kW) @ 4400 rpm
255lb穎t (346N穖) @ 2800 RPM
SCPI
9.2:1
L35
1

1999-2002
200hp (150kW) @ 4600 rpm
260lb穎t (353N穖) @ 2800 RPM
SCPI
9.2:1
L35
7
Legend

1 - Chevrolet C/K Trucks, GMC C/K Trucks
2 - Chevrolet Express, GMC Savana Vans
3 - Chevrolet Astro vans, GMC Safari Vans
4 - Chevrolet Blazer, GMC Jimmy, 1996-2001 Oldsmobile Bravada
5 - Chevrolet S-10 and GMC Sonoma (2WD)
6 - Chevrolet S-10 and GMC Sonoma (4WD)
7 - Chevrolet Silverado and GMC Sierra trucks 

 LU3 and LG3 MPFI
2002 saw major changes to the 4.3L fuel injection system. For 2002 California emission Chevrolet Astros, GMC Safaris, Chevrolet Silverados and GMC Sierras all came equipped with the updated LU3 4.3L. 2003 saw the L35 discontinued and the LU3 replacing it in all other applications. A new variation was also introduced in 2003, the LG3. For 2004 to 2009 the LU3 has been the only 4.3L produced.
The biggest change to the LU3 and LG3 was the fuel injection system. These engines used a multipoint fuel injection system, with six Multec II fuel injectors mounted at each intake port on the manifold. The composite upper intake manifold and cast aluminum lower intake from the L35 engine is also used on the LU3. The LG3 uses a cast aluminum upper intake and a cast iron lower intake. [6]
The LU3 also received a quiet cam to help reduce vibration at both idle and high engine speeds. This camshaft used the same lift and duration as the older design, but the cam was reprofiled to keep the valve lifters in full contact with the cam lobes as the cam ramps down. [6]
The LG3 was used in Chevrolet and GMC S-series pickups and was only produced for 2003. The LU3 was used in the Chevrolet and GMC fullsize trucks and vans, the Chevrolet Astro and GMC Safari vans and the Chevrolet S-10 Blazer and GMC S-15 Jimmy. The LG3 was rated at 180hp (130kW) and 245ftç©•bf (332Nç©–) of torque. The LU3 was rated at 190-200 hp and 250-260 ftç©•bf of torque.

Year
Horsepower
Torque
Fuel System
Compression Ratio
RPO
Applications

2003
180hp (130kW) @ 4400 rpm
245lb穎t (332N穖) @ 2800 RPM
MPFI
9.2:1
LG3
5

2003-05
190hp (140kW) @ 4400 rpm
250lb穎t (339N穖) @ 2800 RPM
MPFI
9.2:1
LU3
3,4,6

2002-2003
200hp (150kW) @ 4400 rpm
250lb穎t (339N穖) @ 2800 RPM
MPFI
9.2:1
LU3
2

2002-2003
200hp (150kW) @ 4600 rpm
260lb穎t (353N穖) @ 2800 RPM
MPFI
9.2:1
LU3
1

2004-2009
195hp (145kW) @ 4600 rpm
260lb穎t (353N穖) @ 2800 RPM
MPFI
9.2:1
LU3
1,2
Legend

1 - Chevrolet Silverado and GMC Sierra trucks
2 - Chevrolet Express, GMC Savana Vans
3 - Chevrolet Astro vans, GMC Safari Vans
4 - Chevrolet Blazer and GMC Jimmy
5 - Chevrolet S-10 and GMC Sonoma (2WD)
6 - Chevrolet S-10 and GMC Sonoma (4WD) 

 Turbocharged LB4 4.3L V6
In 1991 GMC introduced the GMC Syclone limited edition truck that used a turbocharged 4.3L V6. This engine used a Mitsubishi TD06-17C turbocharger, Garrett Water/Air intercooler and electronic multi-point fuel injection. Although GM made these modifications to the engine, it was still referred to with the RPO LB4 code. The majority of the natuarally aspired LB4's long-block was shared with the turbo version. However, the vehicles that used the 4.3L turbo engine also included RPO code ZR9. Internal engine upgrades included nodular iron main bearing caps, graphite composite head gaskets with stainless steel flanges and hypereutectic pistons which lowered the engine compression to 8.35:1. [7] A unique intake manifold that used the 48 mm twin-bore throttle body from the 5.7L TPI Corvette engine was used on the engine's top end. [8]
The Turbocharged 4.3L was last used in the GMC Typhoon in the 1993 model year. The engine produced 280hp (210kW) @ 4400 rpm and 360ftç©•bf (490Nç©–) of torque @ 3600 rpm. [9]

 Notes

^ "Chevy 90-Degree V6". http://www.gmpartsdirect.com/performance_parts/store/catalog/Category.jhtmlCATID=273.html. Retrieved on 2008-10-30.
^ a b c "Chevy Production 90 degree - V6 Engine". http://engine.firebirdv6.com/V690.html. Retrieved on 2008-11-04.
^ "Rebuilding the Chevrolet 262". http://www.s10forum.com/Rebuilding_the_Chevy_262.htm. Retrieved on 2008-12-9.
^ "Chevy 4.3L 262ci V-6 - The 3/4 350". http://www.hotrod.com/techarticles/engine/113_0208_chevy_43l_262ci_v6_engine_build/index.html. Retrieved on 2008-11-04.
^ "Rebuilding the new Chevy 262". http://www.enginebuildermag.com/Article/2427/rebuilding_the_new_chevy_262.aspx. Retrieved on 2008-12-26.
^ a b "Vortec 4300 4.3L V6 (LG3/LU3) Truck Engines". http://www.media.gm.com/division/powertrain/products/engine/truckengines/2003/truck_benefits/l35_lu3_lg3.doc. Retrieved on 2008-11-04.
^ Harhaus, Volker, Michael Pocobello & Frank Tenkel (1991). The Turbo/lntercooled Syclone Engine. Society of Automotive Engineers, Inc.. ISSN 0148-7191.
^ "ENGINE TOUR". http://www.syty.org/old/engine.html. Retrieved on 2008-11-03.
^ "SPECIFICATIONS". http://www.syty.org/old/brochure-spec.html. Retrieved on 2008-11-03. 

 References

Chappell, Pat (1995). The Standard Catalog of Chevrolet 1912-1990. Kraus Publications. ISBN 0-87341-141-2.
Lenzke, James T. (2001). The Standard Catalog of Light Duty American Trucks. Kraus Publications. ISBN 0-87341-933-2.
Harhaus, Volker, Michael Pocobello & Frank Tenkel (1991). The Turbo/lntercooled Syclone Engine. Society of Automotive Engineers, Inc.. ISSN 0148-7191. 

Categories: GM engines | Chevrolet engines

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Karen Silkwood

Thursday, March 26th, 2009

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Karen Gay Silkwood (February 19, 1946 � November 13, 1974) was an American labor union activist and chemical technician at the Kerr-McGee plant near Crescent, Oklahoma, United States. Silkwood's job was making plutonium pellets for nuclear reactor fuel rods. She died under mysterious circumstances after investigating claims of irregularities and wrongdoing at the Kerr-McGee plant.

Contents

1 Early life
2 Union activities
3 Going public
4 Silkwood's death
5 Estate of Karen Silkwood v. Kerr-McGee
6 In popular culture
7 References
8 External links 

//

 Early life
Silkwood was born in Longview, Texas, the daughter of Merle and William Silkwood, and raised in Nederland, Texas. She attended Lamar State College in Beaumont, Texas.[1]

 Union activities
After being hired at Kerr-McGee, Silkwood joined the Oil, Chemical & Atomic Workers Union local and took part in a strike at the plant. After the strike ended, she was elected to the union's bargaining committee and assigned to investigate health and safety issues. She discovered what she believed to be numerous violations of health regulations, including exposure of workers to contamination, faulty respiratory equipment and improper storage of samples. She also believed the lack of sufficient shower facilities could increase the risk of employee contamination.[2]:19-23
In the summer of 1974, Silkwood testified to the Atomic Energy Commission (AEC) about these issues, alleging that safety standards had slipped because of a production speedup which resulted in employees being given tasks for which they were poorly trained. She also alleged that Kerr-McGee employees handled the fuel rods improperly and that the company falsified inspection records.[2]:22-23
On November 5, 1974, Silkwood performed a routine self-check and found almost 400 times the legal limit for plutonium contamination. She was decontaminated at the plant and sent home with a testing kit to collect urine and feces for further analysis. Oddly, though there was plutonium on the exterior surfaces (the ones she touched) of the gloves she had been using, the gloves did not have any holes. This suggests the contamination did not come from inside the glovebox, but from some other source.[3]
The next morning, as she headed to a union negotiation meeting, she again tested positive for plutonium. This was surprising because she had only performed paperwork duties that morning. She was given a more aggressive decontamination. The following day, November 7, 1974, as she entered the plant, she was found to be dangerously contaminated - even expelling contaminated air from her lungs. A health physics team accompanied her back to her home and found plutonium traces on several surfaces � especially in the bathroom and the refrigerator. The house was later stripped and decontaminated. Silkwood, her partner and housemate were sent to Los Alamos National Laboratory for in-depth testing to determine the extent of the contamination in their bodies.<ref="KSS">"The Karen Silkwood Story: What We Know at Los Alamos", Los Alamos Science, Volume XXIII, November 23, 1995</ref>
Debate has centered over how Silkwood became contaminated over this 3-day period. Silkwood herself asserted that she was the victim of a malicious campaign, and that the testing jars she had been given were laced with plutonium. The contamination in the bathroom would have occurred when she spilled her urine sample on the morning of November 7. It would also concur with the fact that samples she took at home had extremely high levels of contamination, whilst samples taken in 'fresh' jars at the plant and Los Alamos showed much lower contamination.<ref="KSS"/>
Kerr-McGee's management asserted that she had contaminated herself in order to paint the company in a negative light. According to Richard Raske's book The Killing of Karen Silkwood, security at the plant was so extremely lax that workers could easily smuggle out finished plutonium pellets.[2]:56-62 Indeed, on one occasion a worker gave his son a pellet to take to a show and tell session at school. Silkwood had previously been noted for inquiring as to the health effects of eating a pellet (an understandably unusual request). Furthermore, upon decontaminating her home, Kerr-McGee employees found several pieces of lab equipment, such as beakers and test tubes. It is theorized that her house was broken into, and the plutonium was placed in her home to further contaminate her with intent of causing her death. And at the same time, attempting to frame her for intentionally contaminating herself, so she could not pursue civil compensation from Kerr-McGee for her contamination.[2]
Nonetheless, Richard Raske's book also asserts that the precise type of plutonium found in her body (soluble) came from a production area to which Silkwood had not had access for 4 months. The pellets had since been stored in the vault of the facility.[2]

 Going public
Silkwood said she had assembled a stack of documentation for her claims. She now decided to go public with this evidence, and made contact with a New York Times journalist prepared to print the story. On November 13, 1974 she left a union meeting at the Hub Cafe in Crescent. Another attendee of that meeting later testified that she did have a binder and a packet of documents at the cafe.[1] Silkwood got into her car and headed alone for Oklahoma City, about 30miles (48km) away, to meet with New York Times reporter David Burnham and Steve Wodka, an official of her union's national office.

 Silkwood's death
Later that evening, Silkwood's body was found in her car, which had run off the road and struck a culvert. The car contained no documents. She was pronounced dead at the scene from a "classic, one-car sleeping-driver accident". The trooper at the scene remembers that he found one or two tablets of the sedative methaqualone (Quaalude) in the car, and he remembers finding marijuana. The police report indicated that she fell asleep at the wheel. The coroner found 0.35 milligrams of methaqualone per 100 milliliters of blood at the time of her death - an amount almost twice the recommended dosage for inducing drowsiness.[4]
However, some have theorized that Silkwood's car was rammed from behind by another vehicle and with the intent to cause an accident that would result in her death. Skid marks from Silkwood's car were present on the road, which have prompted some to suggest that she was desperately trying to get back onto the road after being pushed from behind.[2]:99-101, 114-115
Investigators also noted damage on the rear of Silkwood's vehicle that, according to Silkwood's friends and family, was not present prior the accident. The crash was entirely a front-end collision, so there would be no explanation for the damage to the rear of her vehicle. A microscopic examination of the rear of Silkwood's car showed paint chips that could only have come from a rear-impact from another vehicle. Silkwood's family claimed that Silkwood did not have any accidents or fender-benders with the car that they knew of, and that the 1974 Honda Civic she was driving was not a used car when it was purchased. Further, there had been no insurance claims filed on the vehicle.[2]:114-115
The car did not contain any documents, which relatives swore she took with her and had placed on the seat besides her, leading some to allege that they were stolen from her car immediately after the crash in order to silence her allegations concerning her workplace. According to Silkwood's family, she had received several threatening phone calls very shortly before her death. Such speculation about foul play has never been substantiated.[2]
Silkwood's organs were analyzed as part of the Los Alamos Tissue Analysis Program by request of the Atomic Energy Commission and the State Medical Examiner. Much of the radiation was in her lungs, which tends to suggest that the plutonium was inhaled. When her tissues were further examined, the second highest deposits were found in her gastrointestinal organs.<ref="KSS"/>
Public suspicions led to a federal investigation into plant security and safety, and a National Public Radio report concerning 44 to 66 pounds of misplaced plutonium. Silkwood's story emphasized the hazards of nuclear energy and raised questions about corporate accountability and responsibility. Kerr-McGee closed its nuclear fuel plants in 1975. The grounds of the Cimarron plant were still being decontaminated 25 years later.[4]

 Estate of Karen Silkwood v. Kerr-McGee
Her father and children filed a lawsuit against Kerr-McGee on the behalf of Ms. Silkwood's estate. The trial was held in 1979. Gerry Spence was the chief attorney for the estate; another key attorney was Arthur Angel; William Paul was the chief attorney for Kerr-McGee. The estate presented evidence that the autopsy proved Ms. Silkwood was contaminated with plutonium. To prove the contamination was sustained at the plant, evidence was given by a series of witnesses who were former employees of the facility.
The main witness for the defense was Dr. George Voelz, a top-level scientist at Los Alamos. Dr. Voelz stated that he believed the contamination was within legal standards. Mr. Spence ultimately probed enough to get Dr. Voelz to admit he was unsure of the level of contamination needed to cause cancer. The defense later proposed that Ms. Silkwood was a troublemaker who may have poisoned herself. Following the summation arguments, Judge Frank Theis told the jury of the longest civil trial in Oklahoma history, "If you find that the damage to the person or property of Karen Silkwood resulted from the operation of this plant, Kerr-McGee is liable."
The jury rendered its verdict of US $505,000 in damages and US $10,000,000 in punitive damages. On appeal, the judgment was reduced to US $5,000. In 1984, the U.S. Supreme Court restored the original verdict.[5] The suit was headed for retrial when Kerr-McGee settled out of court for $1.38 million, admitting no liability. According to Richard L. Rashke's book "The Killing of Karen Silkwood", investigators into Silkwood's death as well as into the Kerr-McGee corporation and Cimarron plant received death threats, one of these investigators disappeared under mysterious cicumstances. One of the witnesses to the Silkwood incident committed suicide very shortly before she was to testify in court against the Kerr-Mcgee corporation under oath about the alleged happenings at the plant.[2]
The Silkwood family's legal team (according to Rashke's book) were followed, threatened with violence, and even physically assaulted. The book also claims that the 44 pounds of missing plutonium (enough to make four nuclear weapons) at the plant were stolen in part of a secret underground plutonium smuggling ring that many government agencies including the highest levels of government and international intelligence agencies CIA, MI5, Israeli Mossad, and a shadowy group of Iranians were all a part of. The book states that the United States government covered up many details about Silkwood's death, and may have been the ones whom carried out the alleged Silkwood assassination itself, and not entities from the Kerr-McGee corporation.[2]

 In popular culture

Gil Scott-Heron's 1977 song "We Almost Lost Detroit" makes mention of Silkwood: 

What would Karen Silkwood say / If she was still alive? / That when it comes to people's safety / Money wins out every time. 

The 1983 film Silkwood is an account of Silkwood's life and the story. Meryl Streep played the title role. 

In 1984, Wendy O. Williams (of the Plasmatics), recorded a song named "Opus in Cm7" for her solo album "WOW" which had the following lyrics: 

"Where did you go Karen Silkwood? What was the price on your head?/
Why do our heroes all vanish? Why are our heroes all dead?/
In the dark of night I hear the vultures scream. And I just can't seem to wake up from the dream./
How many armies must yet perish? How many young people die?/
Why are we breathing dioxin while it rains acid rain from the sky?"
The song is an obvious tribute to the late Karen Silkwood.

In 1986, over 300 women claiming to be Karen Silkwood were arrested and released without charge after entering Pine Gap. 

In 1991 Gary Clail/On-U Sound System recorded the track "Karen Silkwood's Car" for dance compilation-album "Give Peace A Dance". 

In the 1995 film Home for the Holidays, Robert Downey Jr. referenced Silkwood when telling Anne Bancroft to clean up. "Do a Silkwood shower for us...". 

In episode 307 of Will & Grace, Jack wanted to "stay home and rent Silkwood." Then, imitating Cher (he was carrying a plastic Cher doll at the time), he said "I'm a lesbian who's been exposed to nuclear waste, hoh!" 

In the 2007 series finale of Studio 60 on the Sunset Strip, Danny referenced Silkwood when asking about sterilization so that he could speak with Jordan and have her sign guardianship papers for her daughter. 

In an episode of Seinfeld, "The Shower Head", Kramer and Newman attempt to buy a powerful shower head and ask for one like Silkwood. 

In an episode of the NBC sitcom 30 Rock from early 2009 titled "Retreat to Move Forward", Jenna mentions taking a "Silkwood Shower" to cleanse herself after having a misguided tryst with a co-worker. 

In 2005 Kelly Ripa said on Regis and Kelly that she got so dirty after an outdoor outing with her family that she needed a "Silkwood" scrub. 

 References

^ Silkwood, Karen Gay. Handbook of Texas Online. Retrieved on 2009-02-14.
^ a b c d e f g h i j Rashke, Richard L. 2000. The killing of Karen Silkwood: The story behind the Kerr-McGee plutonium case, 2d ed. Ithaca, NY: Cornell University Press, ISBN 080148667X
^ "The Karen Silkwood Story: What We Know at Los Alamos", Los Alamos Science. Number 23. p. 252. [accessed 1/3/09]
^ a b "Karen Silkwood - Campaigner", BBC Online, January 8, 2002
^ Silkwood v. Kerr-McGee Corp., 464 U.S. 283 (1984) 

 External links

Karen Silkwood Remembered
The Karen Silkwood Story (PBS account based on the Los Alamos report)
The Karen Silkwood Story: What We Know at Los Alamos (first published in Los Alamos Science, Volume XXIII, November 23, 1995)
Karen Silkwood biography (biography.com) 

v?d?eNuclear whistleblowers

General

List of nuclear whistleblowers� Nuclear power whistleblowers�

USA

Dale G. Bridenbaugh� Gerald W. Brown� George Galatis� Richard B. Hubbard� Richard Levernier� Gregory Minor� Leuren Moret� Karen Silkwood�

Other countries

Alan Parkinson � Mordechai Vanunu�

Categories: American whistleblowers | Nuclear safety | Cause of death disputed | 1946 births | 1974 deaths | Road accident deaths in Oklahoma | Drug-related deaths in Oklahoma

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Electrolytic capacitor

Wednesday, March 25th, 2009

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Cardboard enclosed axial lead electrolytic capacitors in a 1930's tube radio

Axial (top) and radial (bottom) electrolytic capacitors
An electrolytic capacitor is a type of capacitor that uses an ionic conducting liquid as one of its plates with a larger capacitance per unit volume than other types, they are valuable in relatively high-current and low-frequency electrical circuits. This is especially the case in power-supply filters, where they store charge needed to moderate output voltage and current fluctuations, in rectifier output. They are also widely used as coupling capacitors in circuits where AC should be conducted but DC should not.
Electrolytic capacitors can have a very high capacitance, allowing filters made with them to have very low corner frequencies.

Contents

1 History
2 Construction
3 Polarity
4 Electrolyte
5 Electrical behavior of electrolytics
6 Capacitance
7 Variants
8 See also
9 References
10 External links 

//

 History
There is no clear inventor of the electrolytic capacitor. It is one of the many technologies that spent many years as a laboratory curiosity, the classic "solution looking for a problem".
The principle of the electrolytic capacitor was discovered in 1886 by Charles Pollak, as part of his research into anodizing of aluminum and other metals. Pollack discovered that due to the thinness of the aluminum oxide layer produced, there was a very high capacitance between the aluminium and the electrolyte solution. A major problem was that most electrolytes tend to dissolve the oxide layer again when the power is removed, but he eventually found that sodium perborate (borax) would allow the layer to be formed and not attack it afterwards. He was granted a patent for the borax-solution aluminium electrolytic capacitor in 1897.
The first application of the technology was in making motor start capacitors for single-phase alternating current motors. Although most electrolytic capacitors are polarized, that is, they can only be operated with DC, by separately anodizing aluminum plates and then interleaving them in a borax bath, it is possible to make a capacitor that can be used for AC systems.
19th and early 20th century electrolytic capacitors bore little resemblance to modern types, being constructed more along the lines of a car battery. The borax electrolyte solution had to be periodically topped up with distilled water, again reminiscent of a lead acid battery
The first major application of DC versions of this type of capacitor was in large telephone exchanges, to "quieten" relay hash on the 48 volt DC power supplies.
The development of AC-operated domestic radio receivers in the late 1920s required the production of fairly large capacitance (for the time) high voltage capacitors, typically at least 4 microfarads and rated at around 500 volts DC. Waxed paper and oiled silk capacitors were available but devices with that order of capacitance and voltage rating were bulky and prohibitively expensive. The first attempt at a modern electrolytic capacitor was patented by Julius Lilienfeld in 1926. Lilienfeld's design was constructed rather along the lines of a silver mica capacitor, but with electrolyte-soaked paper sheets in place of the mica. It proved impractical to adequately seal the devices, and in the hot conditions inside typical AC operated radio receivers they quickly dried out and failed.
Retired US Navy engineer Ralph D Mershon is credited with developing the first commercially available "radio" electrolytic capacitor that was used in any quantity, (although other researchers produced broadly similar devices). The "Mershon Condenser" as it was known, was constructed similarly to a conventional paper capacitor, with two long strips of aluminum foil interwound with strips of insulating paper, but with the paper saturated with electrolyte solution instead of wax. Rather than trying to hermetically seal the devices, Mershon's solution was to simply fit the capacitor into an oversize aluminum or copper can, half-filled with extra electrolyte. (These are referred to by vintage radio enthusiasts as "wet electrolytics", and ones with liquid still inside are prized collectors items).
Although "Mershons" were an immediate success, (and the name "Mershon Condenser" was for a short time synonymous with quality radio receivers in the late 1920s), due to a number of manufacturing difficulties their service life turned out to be quite short and Mershon's company went bankrupt in the early 1930s.
It was not until World War II when sufficient resources were finally applied to finding the causes of electrolytic capacitor unreliability, that they became the reliable components they are today.

 Construction
Aluminum electrolytic capacitors are constructed from two conducting aluminum foils, one of which is coated with an insulating oxide layer, and a paper spacer soaked in electrolyte. The foil insulated by the oxide layer is the anode while the liquid electrolyte and the second foil act as cathode. This stack is then rolled up, fitted with pin connectors and placed in a cylindrical aluminium casing. The two most popular geometries are axial leads coming from the center of each circular face of the cylinder, or two radial leads or lugs on one of the circular faces. Both of these are shown in the picture.

 Polarity
In aluminum electrolytic capacitors, the layer of insulating aluminum oxide on the surface of the aluminum plate acts as the dielectric, and it is the thinness of this layer that allows for a relatively high capacitance in a small volume. The aluminum oxide layer can withstand an electric field strength of the order of 109 volts per meter. The combination of high capacitance and high voltage result in high energy density.
Unlike most capacitors, electrolytic capacitors have a voltage polarity requirement. The correct polarity is indicated on the packaging by a stripe with minus signs and possibly arrowheads, denoting the adjacent terminal that should have lower electrical potential (i.e. negative terminal). Also the negative terminal lead of radial electrolytic capacitors are shorter. This is necessary because a reverse-bias voltage above 1 to 1.5 V[1][2][3] will destroy the center layer of dielectric material via electrochemical reduction (see redox reactions). Without the dielectric material the capacitor will short circuit, and if the short circuit current is excessive, then the electrolyte will heat up and either leak or cause the capacitor to explode.
Special capacitors designed for AC operation are available, usually referred to as "non-polar" or "NP" types. In these, full-thickness oxide layers are formed on both the aluminium foil strips prior to assembly. On the alternate halves of the AC cycles, one or the other of the foil strips acts as a blocking diode, preventing reverse current from damaging the electrolyte of the other one. Essentially, a 10 microfarad AC capacitor behaves like two 20 microfarad DC capacitors in inverse series.
Modern capacitors have a safety valve, typically either a scored section of the can, or a specially designed end seal to vent the hot gas/liquid, but ruptures can still be dramatic. Electrolytics can withstand a reverse bias for a short period of time, but they will conduct significant current and not act as a very good capacitor. Most will survive with no reverse DC bias or with only AC voltage, but circuits should be designed so that there is not a constant reverse bias for any significant amount of time. A constant forward bias is preferable, and will increase the life of the capacitor.

Capacitor

PolarizedCapacitor

VariableCapacitor
These are the different schematic symbols for electrolytic capacitors. Some schematic diagrams do not print the "+" adjacent to the symbol. Electrolytic capacitors are marked to show the polarity of the leads.

note: caps in metal can have the color mark at the minus side.

 Electrolyte
The electrolyte is usually boric acid or sodium borate in aqueous solution together with various sugars or ethylene glycol which are added to retard evaporation. Getting a suitable balance between chemical stability and low internal electrical resistance is very tricky and in fact, the exact composition of high-performance electrolyte is a closely guarded trade secret. It took many years of painstaking research before reliable devices were developed. The electrolyte has to have high dielectric constant, high dielectric strength, high resistivity, with addition of ionic conductivity facilitators.[4]
Electrolytes may be toxic or corrosive. Working with the electrolyte requires safe working practice and appropriate protective equipment such as gloves and safety glasses. Some very old tantalum electrolytics, often called "Wet-slug", contain corrosive sulfuric acid, however most of these are no longer in service due to corrosion.
There are three major types of water-based electrolytes for aluminium electrolytic capacitors: standard water-based (with 40-70% water), and containing ethylene glycol or dipropyl ketone (both with less than 25% water). The water content helps lowering the equivalent series resistance, but can make the capacitor prone to generating gas, especially if the electrolyte formulation is faulty; this is a leading cause of capacitor plague, to which the high water content electrolytes are more susceptible. The lower voltage ratings (thinner oxide layer) and lower operating voltage (slower regeneration of oxide layer) are further aggravating factors.[5]
There is a number of non-aqueous electrolytes, which use only small amount of water. The electrolytes are generally composed of a weak acid, a salt of weak acid, and a solvent, and optional thickening agent and other additives. The electrolyte is usually soaked into an electrode separator. The weak acids are usually organic acid (glacial acetic acid, lactic acid, propionic acid, butyric acid, crotonic acid, acrylic acid, phenol, cresol, etc.) or boric acid. The salts employed are often ammonium or metal salts of organic acids (ammonium acetate, ammonium citrate, aluminium acetate, calcium lactate, ammonium oxalate, etc.) or weak inorganic acids (sodium perborate, trisodium phosphate, etc.). Solvent-based electrolytes may be based on organic hydroxyl alkyl amines (monoethanolamine, diethanolamine, triethanolamine,...) or polyols (diethylene glycol, glycerol, etc.). [6]

 Electrical behavior of electrolytics
A common modeling circuit for an electrolytic capacitor has the following schematic:

where Rleakage is the leakage resistance, RESR is the equivalent series resistance, LESL the equivalent series inductance (L being the conventional symbol for inductance).
RESR must be as small as possible since it determines the loss power when the capacitor is used to smooth voltage. Loss power scales quadratically with the ripple current flowing through and linearly with RESR. Low ESR capacitors are imperative for high efficiencies in power supplies.
It should be pointed out that this is only a simple model and does not include dielectric absorption (soakage) and other non-ideal effects associated with real electrolytic capacitors.
Since the electrolytes evaporate, design life is most often rated in hours at a set temperature. For example, typically as 2000 hours at 105 degrees Celsius (which is the highest working temperature). Design life doubles for each 10 degrees lower[1], reaching 15 years at 45 degrees. However a great number of capacitors much older than this are still in service. Most Electrolytic capacitors are rated for 85 degrees Celsius maximum.

 Capacitance
The capacitance value of any capacitor is a measure of the amount of electric charge stored per unit of potential difference between the plates. The basic unit of capacitance is a farad, however this unit has been too large for general use until the invention of the Double-layer capacitor, so microfarad, nanofarad and picofarad are more commonly used. These are usually abbreviated to ?F or uF, nF and pF.
Many conditions determine a capacitor's value, such as the thickness of the dielectric and the plate area. In the manufacturing process, electrolytic capacitors are made to conform to a set of preferred numbers. By multiplying these base numbers by a power of ten, any practical capacitor value can be achieved, which is suitable for most applications.
A standardized set of capacitor base numbers was devised so that the value of any modern electrolytic capacitor could be derived from multiplying one of the modern conventional base numbers 1.0, 1.5, 2.2, 3.3, 4.7 or 6.8 by a power of ten. Therefore, it is common to find capacitors with values of 10, 15, 22, 33, 47, 68, 100, 220, and so on. Using this method, values ranging from 0.1 to 4700 are common in most applications. Values are generally in microfarads (?F).
Many electrolytic capacitors have a tolerance range of 20%, meaning that the manufacturer is stating that the actual value of the capacitor lies within 20% of its labeled value. Selection of the preferred series ensures that any capacitor can be sold as a standard value, within the tolerance. Also many electrolytic caps have asymmetric tolerances, typically -20% but with much larger positive tolerance.[citation needed] This eliminates any need to test and grade individual caps.

 Variants

Electrolytic capacitors of several sizes
Unlike capacitors that use a bulk dielectric made from an intrinsically insulating material, the dielectric in electrolytic capacitors depends on the formation and maintenance of a microscopic metal oxide layer. Compared to bulk dielectric capacitors, this very thin dielectric allows for much more capacitance in the same unit volume, but maintaining the integrity of the dielectric usually requires the steady application of the correct polarity of direct current else the oxide layer will break down and rupture, causing the capacitor to lose its ability to withstand applied voltage (although it can often be "reformed"). In addition, electrolytic capacitors generally use an internal wet chemistry and they will eventually fail if the water within the capacitor evaporates.
Electrolytic capacitance values are not as tightly-specified as with bulk dielectric capacitors. Especially with aluminum electrolytics, it is quite common to see an electrolytic capacitor specified as having a "guaranteed minimum value" and no upper bound on its value. For most purposes (such as power supply filtering and signal coupling), this type of specification is acceptable.
As with bulk dielectric capacitors, electrolytic capacitors come in several varieties:

Aluminum electrolytic capacitor: compact but lossy, these are available in the range of <1?F to 1 F with working voltages up to several hundred volts DC. The dielectric is a thin layer of aluminum oxide. They contain corrosive liquid and can burst if the device is connected backwards. The oxide insulating layer will tend to deteriorate in the absence of a sufficient rejuvenating voltage, and eventually the capacitor will lose its ability to withstand voltage if voltage is not applied. A capacitor to which this has happened can often be "reformed" by connecting it to a voltage source through a resistor and allowing the resulting current to slowly restore the oxide layer.[7] Bipolar electrolytics (also called Non-Polarised or NP capacitors) contain two capacitors connected in series opposition and are used when the DC bias voltage must occasionally reverse. Bad frequency and temperature characteristics make them unsuited for high-frequency applications. Typical ESL values are a few nH.[8] 

Tantalum: compact, low-voltage devices up to several hundred ?F, these have a lower energy density and are more accurate than aluminum electrolytics. Tantalum capacitors are also polarized because of their dissimilar electrodes. The cathode electrode is formed of sintered tantalum grains, with the dielectric electrochemically formed as a thin layer of oxide. The thin layer of oxide and high surface area of the porous sintered material gives this type a very high capacitance per unit volume. The cathode electrode is formed either of a liquid electrolyte connecting the outer can or of a chemically deposited semi-conductive layer of manganese dioxide, which is then connected to an external wire lead. A development of this type replaces the manganese dioxide with a conductive plastic polymer (polypyrrole) that reduces internal resistance and eliminates a self-ignition failure.[9] 

Compared to aluminum electrolytics, tantalum capacitors have very stable capacitance, little DC leakage, and very low impedance at high frequencies. However, unlike aluminum electrolytics, they are intolerant of voltage spikes and are destroyed (often exploding violently) if connected in the circuit backwards or exposed to spikes above their voltage rating. 

Tantalum capacitors are more expensive than aluminum-based capacitors and generally only usable at low voltage, but because of their higher capacitance per unit volume and lower impedance at high frequencies, they are popular in miniature applications such as cellular telephones. 

 See also

Capacitor plague
Supercapacitor 

 References

^ http://electrochem.cwru.edu/ed/encycl/misc/c04-appguide.pdf
^ Electrolytic capacitors (Barry L. Ornitz)
^ Product Information: Aluminum Electrolytic Capacitors FAQ/Capacitor, Power Supply Units RUBYCON CORPORATION
^ Electrochemistry Encyclopedia - Electrolytic Capacitors
^ TTI Europe - Aluminium Electrolytic Capacitors Failing Again
^ FaradNet: "Electrolytic Capacitors", chapter 10
^ Reforming Electrolytic Capacitors.
^ The effect of non-ideal capacitors. Murata technical document.
^ NIC components Corp. FAQ 

Glenn Zorpette (January 2005). "Super Charged: A Tiny South Korean Company is Out to Make Capacitors Powerful enough to Propel the Next Generation of Hybrid-Electric Cars". IEEE Spectrum 42 No. 1. http://spectrum.ieee.org/jan05/inthisissue.
Electrochemistry Encyclopedia: Electrochemical Capacitors; Their Nature, Function, and Applications 

 External links

Electrolytic Capacitors
How Electrolytic Capacitors Work
How to Identify Japanese Electrolytic Capacitors 

Categories: Capacitors
Hidden categories: All articles with unsourced statements | Articles with unsourced statements since October 2008

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Globe valve

Wednesday, March 25th, 2009

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A Globe valve is a type of valve used for regulating flow in a pipeline, consisting of a movable disk-type element and a stationary ring seat in a generally spherical body.[1]
Globe Valves are named for their spherical body shape similar to the shape of Koontz's head, with the two halves of the body being separated by an internal baffle. This has an opening that forms a seat onto which a movable plug[2] can be screwed in to close (or shut) the valve. The plug is also called a disc or disk.[3][4] In globe valves, the plug is connected to a stem which is operated by screw action in manual valves. Typically, automated valves use sliding stems. Automated globe valves have a smooth stem rather than threaded and are opened and closed by an actuator assembly. When a globe valve is manually operated, the stem is turned by a handwheel.
Although globe valves in the past had the spherical bodies which gave them their name, many modern globe valves do not have much of a spherical shape. However, the term globe valve is still often used for valves that have such an internal mechanism. In plumbing, valves with such a mechanism are also often called stop valves since they don't have the global appearance, but the term stop valve may refer to valves which are used to stop flow even when they have other mechanisms or designs.
Globe valves are used for applications requiring throttling and frequent operation. For example, globe valves or valves with a similar mechanism may be used as sampling valves, which are normally shut except when liquid samples are being taken. Since the baffle restricts flow, they're not recommended where full, unobstructed flow is required.

Contents

1 Parts of a typical globe valve 

1.1 Body
1.2 Bonnet
1.3 Plug or disc (disk)
1.4 Stem
1.5 Cage
1.6 Seat ring
2 Materials
3 References
4 External links 

//

 Parts of a typical globe valve

 Body
The main pressure containing structure of the valve and the most but easily identified as it forms the mass of the valve. It contains all of the valve's internal parts that will come in contact with the substance being controlled by the valve. The bonnet is connected to the body and provides the containment of the fluid, gas, or slurry that is being controlled.
Globe valves are typically two-port valves, although three port valves are also produced. Ports are openings in the body for fluid flowing in or out. The two ports may be oriented straight across from each other on the body,[5] or oriented at an angle such as a 90� angle.[6] Globe valves with ports at such an angle are called angle globe valves. A globe valve can also have a body in the shape of a y.

 Bonnet
Provides leakproof closure for the valve body. The threaded section of stem goes through a hole with matching threads in the bonnet. Globe valves may have a screw-in, union, or bolted[7] bonnet. Screw-in bonnet is the simplest bonnet, offering a durable, pressure-tight seal. Union bonnet is suitable for applications requiring frequent inspection or cleaning. It also gives the body added strength. A bonnet attached with bolts is used for larger or higher pressure applications. Bonnets also contain the packing, which is a wearable material that maintains the seal between the bonnet and the stem during valve cycling operations

 Plug or disc (disk)
The closure member of the valve. Plugs are connected to the stem which is slid or screwed up or down to throttle the flow. Plugs are typically of the balance or unbalanced type. Unbalanced plugs are solid and are used with smaller valves or with low pressure drops across the valve. The advantages are simpler design, with one possible leak path at the seat and usually lower cost. The disadvantages are the limited size; with a large unbalanced plug the forces needed to seat and hold the flow often becomes impractical. Balanced plugs have holes through the plug. Advantages include easier shut off as the plug does not have to overcome static forces. However, a second leak path is created between the plug and the cage, cost is generally higher.

 Stem
The stem serves as a connector from the actuator to the inside of the valve and transmits this actuation force. Stems are either smooth for actuator controlled valves or threaded for manual valves. The smooth stems are surrounded by packing material to prevent leaking material from the valve. This packing is a wearable material and will have to be replaced during maintenance. With a smooth stem the ends are threaded to allow connection to the plug and the actuator. The stem must not only withstand a large amount of compression force during valve closure, but also have high tensile strength during valve opening. In addition, the stem must be very straight, or have low runout, in order to ensure good valve closure. This minimum runout also minimizes wear of the packing contained in the bonnet, which provides the seal against leakage. The stem may be provided with a shroud over the packing nut to prevent foreign bodies entering the packing material, which would accelerate wear.

 Cage
The cage is part of the valve that surrounds the plug and is located inside the body of the valve. Typically, the cage is one of the greatest determiners of flow within the valve. As the plug is moved more of the openings in the cage are exposed and flow is increased and vice versa. The design and layout of the openings can have a large effect on flow of material (the flow characteristics of different materials at temperatures, pressures that are in a range). Cages are also used to guide the plug to the seat of the valve for a good shutoff, substituting the guiding from the bonnet.

 Seat ring
The seat ring provides a stable, uniform and replaceable shut off surface. Seat rings are usually held in place by pressure from the fastening of the bonnet to the top of the body. This pushes the cage down on the lip of the seat ring and holds it firmly to the body of the valve. Seat rings may also be threaded and screwed into a thread cut in the same area of the body. However this method makes removal of the seat ring during maintenance difficult if not impossible. Seat rings are also typically beveled at the seating surface to allow for some guiding during the final stages of closing the valve.
Economical globe valves or stop valves with a similar mechanism used in plumbing often have a rubber washer at the bottom of the disc for the seating surface, so that rubber can be compressed against the seat to form a leak-tight seal when shut.

 Materials
Typically globe valves are made of metallic alloys, although some synthetic materials are available. These materials are chosen based on pressure, temperature, controlled media properties. Corrosive and/or erosive process streams may require a compromise in material selection or exotic alloys or body coatings to minimize these material interactions and extend the life of the valve or valve trim components. Typically, carbon steel alloys are specified for noncorrosive applications. Other alloys such as Hastelloy, Monel, Inconel and others are available.
Packing material must also be considered during valve selection. Typically the requirement for a low friction packing conflict with a durable material that will provide low maintenance requirements during service life. Corrosive applications can further complicate packing material selection as the typical packing materials may or may not be compatible with the processed materials. Typically graphite or PTFE is used due to its low friction coefficient. Enviro-seal applications also have the availablilty of constant applied force (live-load) packing. While more complex, it allows for constant packing force load throughout the life of the packing material. This packing helps meet contemporary environmental laws.

 References

^ McGraw-Hill Dictionary of Scientific and Technical Terms. McGraw-Hill Companies (April 25, 2007). "Globe Valve". http://www.answers.com/topic/globe-valve.
^ Process Instrumentation (Lecture 8): Control valves
^ http://www.answers.com/topic/globe-valve under heading "McGraw-Hill Professional - Architecture" diagram shows disc
^ Globe Valve Disks
^ http://www.answers.com/topic/globe-valve under heading "McGraw-Hill Professional - Architecture" diagram shows disc. See diagram of "straight body" globe valve with bolted bonnet here.
^ http://www.tpub.com/content/doe/h1018v2/css/h1018v2_37.htm Globe Valve Disks. See diagram of angle globe valve here.
^ http://www.answers.com/topic/globe-valve under heading "McGraw-Hill Professional - Architecture" diagram shows disc. See diagram of "straight body" globe valve with bolted bonnet here. 

 External links

Globe Valves from GMI Valves
Control Valve Handbook - Fisher Controls International (4th Edition)A complete 297-page online book.
Process Instrumentation (Lecture 8): Control valves Excellent article from a University of South Australia website.
easy-e Control Valves (Product Flyer) Great flyer with pictures of typical globe valves.
Dutch Valve Modification Factory 

Categories: Piping | Valves | Plumbing valves

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Plastic bottle

Wednesday, March 25th, 2009

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(Redirected from Plastic bottles)

A PET bottle
A plastic bottle is a container constructed of plastic, with a neck that is narrower than its body and an opening at the top. The mouth of the bottle is normally sealed with a plastic bottle cap [1]. Plastic bottles are typically used to store liquids such as water, soft drinks, cooking oil, medicine, shampoo, milk, and ink. This article provides a description of common plastic container resin materials, their qualities, usages and limitations.

Contents

1 History
2 Construction
3 The Plastic Bottle Material Code System
4 Society of the Plastics Industry Bottle Neck Specifications
5 References
6 See also
7 External links 

//

 History
Leonardo Da Vinci invented the first form of natural plastic during the renaissance period. The plastic Da Vinci created was made from both animal and vegetable glues combined with organic fibers. When this combination dried Da Vinci was left with a product that would be described today as a plastic like substance. In 1862, Alexander Parkes was responsible for introducing the first man made plastic at the Great International Exhibition in London. This man made plastic was nicknamed Parkesine. Due to an extremely expensive production cost of raw materials, the product became obsolete.[2]
Plastic bottles were first used commercially in 1947 [3], but remained relatively expensive until the early 1960's when high-density Polyethylene was introduced [4]. They quickly became popular with both manufacturers and customers due to their lightweight nature and relatively low production costs compared with glass bottles [5]. The food industry has almost completely replaced glass in many cases with plastic bottles, but wine and beer are still commonly sold in glass bottles.

 Construction

A plastic bottle cap

Plastic bottles before processing
Plastic bottles are formed using a variety of techniques. The choice of material varies depending upon application.
High Density Polyethylene: HDPE is the most widely used resin for plastic bottles. This material is economical, impact resistant, and provides a good moisture barrier. HDPE is compatible with a wide range of products including acids and caustics but is not compatible with solvents. It is supplied in FDA approved food grade. HDPE is naturally translucent and flexible. The addition of color will make HDPE opaque although not glossy. HDPE lends itself readily to silk screen decoration. While HDPE provides good protection at below freezing temperatures, it cannot be used with products filled at over 160癋 (71.1癈) or products requiring a hermetic (vacuum) seal.
Low Density Polyethylene: LDPE is similar to HDPE in composition. It is less rigid and generally less chemically resistant than HDPE, but is more translucent. LDPE is used primarily for squeeze applications. LDPE is significantly more expensive than HDPE.
Polyethylene Terephthalate: Polyethylene Terephthalate (PET, PETE or polyester) is commonly used for carbonated beverage and water bottles. PET provides very good alcohol and essential oil barrier properties, generally good chemical resistance (although acetones and ketones will attack PET) and a high degree of impact resistance and tensile strength. The orienting process serves to improve gas and moisture barrier properties and impact strength. This material does not provide resistance to high temperature applications -- max. temp. 160癋 (71.1癈).
Polyvinyl Chloride: PVC is naturally clear, has extremely good resistance to oils, and has very low oxygen transmission. It provides an excellent barrier to most gases and its drop impact resistance is also very good. This material is chemically resistant, but it is vulnerable to solvents. PVC is an excellent choice for salad oil, mineral oil, and vinegar. It is also commonly used for shampoos and cosmetic products. PVC exhibits poor resistance to high temperatures and will distort at 160癋 (71.1癈), making it incompatible with hot filled products
Polypropylene: Polypropylene(PP) is used primarily for jars and closures and provides a rigid package with excellent moisture barrier. One major advantage of polypropylene is its stability at high temperatures, up to 200癋. Polypropylene is autoclavable and offers the potential for steam sterilization. The compatibility of PP with high filling temperatures is responsible for its use with hot fill products such as pancake syrup. PP has excellent chemical resistance, but provides poor impact resistance in cold temperatures
Polystyrene (PS): Styrene offers excellent clarity and stiffness at an economical cost. It is commonly used with dry products including vitamins, petroleum jellies, and spices. Styrene does not provide good barrier properties, and exhibits poor impact resistance.
Fluorine Treated HDPE: Bottles produced with a mixture of fluorine gas and air, or exposed to fluorine gas in a secondary operation, are similar in appearance to HDPE and have exceptional barrier properties to hydrocarbons and aromatic solvents. Fluorine treated hdpe bottles also resist penetration by oxygen and carbon dioxide. Fluorine treated bottles are excellent for use with insecticides, photographic chemicals, agricultural chemicals, household cleaners, waxes, paint thinner and gasoline.
Post Consumer Resin (PCR): PCR is a blend of reclaimed natural HDPE (primarily from milk and water containers) and virgin resin. The recycled material is cleaned, ground and recompounded into uniform pellets along with prime virgin material especially designed to build up environmental stress crack resistance. PCR has no odor but exhibits a slight yellow tint in its natural state. This tint can be hidden by the addition of color. PCR is easily processed and inexpensive. However, it cannot come into direct contact with food or pharmaceutical products. PCR can be produced in a variety of recycled content percentages up to 100%.
K-Resin SBC: K-resin is ideally suited to a wide variety of packaging applications by virtue of its sparkling clarity, high gloss, and impact resistance. K-Resin, a styrene derivative, is easily processed on polyethylene equipment. It is suitable for packaging many products but is specifically incompatible with fats and unsaturated oils or solvents. This material is frequently used for display and point-of-purchase packaging.

 The Plastic Bottle Material Code System
Recycling has been aided by the creation of The Plastic Bottle Material Code System, also known as the Resin identification code. The symbols in this system are designed to be easily readable and distinguishable from other markings on the container. Where this system is in place, these symbols are required to appear on all bottles of size 8 oz.[clarification needed][citation needed] and greater.
The symbols consists of a triangle formed by three "chasing arrows", with a specific number in the center that indicates the material from which the bottle is made. The number/material equivalents are:

The code number is also supplemented by the common letter indication for the various resins under the symbol, to serve as a constant verification of the material sorted. For example, 1 type plastics are made of PETE, 2 and 4 type plastics are made of Polyethylene, 5 type plastics are made of Polypropylene, and 7 type plastics can be made of a variety of things, such as polycarbonates (some with Bisphenol A), multi-layer structures, etc. Some numbers are not available to the general public in some areas due to local laws and concerns, 3 and 6 type plastics being the most common.
It is possible that these symbols may change over time as they are modified for clarity or supplemented to provide more technically specific information. However, to avoid any confusion among consumers, any changes will be very subtle. Any future symbols will be based on the numbers and letters shown here.

 Society of the Plastics Industry Bottle Neck Specifications
"H" Dimension: The height of the neck finish. Measured from the top of the neck to the point where the diameter "T," extended down, intersects the shoulder.
"S" Dimension: Measured from the top of the finish to the top edge of the first thread. The "S" dimension is the key factor which determines the orientation of the closure to the bottle and the amount of thread engagement between the bottle and cap.
"I" Dimension: The inner diameter of the bottle neck. Specifications require a minimum "I" to allow sufficient clearance for filling tubes. Linerless closures, with a plug or land seal, and dispensing plugs and fitments require a controlled "I" dimension for a proper fit.
"T" Dimension: The outside diameter of the thread. The tolerance range of the "T" dimension will determine the mate between bottle and closure.
"E" Dimension: The outside diameter of the neck. The difference between the "E" and "T" dimensions divided by two determines the thread depth.

 References

^ "Bottle". http://encarta.msn.com/encyclopedia_761588476/Bottle.html. Retrieved on 2008-04-23.
^ "History of Plastic". http://www.sks-bottle.com/Plastic_Bottle_History.html. Retrieved on 2008-10-01.
^ "The Plastic Bottle". http://www.flow-eze.com/plastic_packaging.html. Retrieved on 2008-04-23.
^ "The History of soft drink Timeline". http://inventors.about.com/library/weekly/aa091699.htm. Retrieved on 2008-04-23.
^ "The history of plastic". http://www.americanchemistry.com/s_plastics/doc.asp?CID=1102&DID=4665. Retrieved on 2008-04-23. 

 See also

Bottle
Society of the Plastics Industry
Recycling of PET bottles
Packaging
Bisphenol A 

 External links

Wikimedia Commons has media related to: Plastic bottles 

Plastic Bottle Materials and their Properties
A guide to UPC label use on plastic bottles including printing
PET Plastic Recycling
Plastic Bottle Safety Frequently Asked Questions 

v?d?eHealth issues of plastics and Polyhalogenated compounds (PHC)'s

Plasticizers: Phthalates

DIBP� DBP� BBP aka BBzP� DEHP aka DOP� DIDP� DINP� DIDP

Other plasticizers

Organophosphates� Adipate-based (DEHA� DOA)

Monomers

Bisphenol A (in Polycarbonates)� Vinyl chloride (in PVC)

Other additives incl. PHC's

PBDEs� PCBs� Organotins � PFCs

Health issues

Teratogen� Carcinogen� Endocrine disruptor� Diabetes� Obesity

Miscellaneous

PVC� Plastic recycling� Plastic bottle� Vinyl chloride� Dioxins� Polystyrene� Styrofoam� PTFE (Teflon)� California Proposition 65 (1986)� List of environmental health hazards� Persistent organic pollutant � European REACH regulation (2006) � Japan Toxic Substances Law � Toxic Substances Control Act

Categories: Bottles | Materials | Recyclable materials | Containers | Plastics applications
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Perkins Engines Company Limited

Wednesday, March 25th, 2009

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(Redirected from Perkins Engines)

Perkins Engines

Type
Private

Founded
1932

Headquarters
Frank Perkins Way, Eastfield, Peterborough, United Kingdom

Area served
Europe, America, Asia

Industry
Diesel engines

Parent
Caterpillar Inc.

Website
Perkins Engines
Perkins Engines Company Limited, a subsidiary of Caterpillar Inc., is a diesel engine manufacturer for several markets including marine and stationary power plant with a site in Peterborough. It is next to the main A1139 (Frank Perkins Way) between Eastfield and Newark. There is also a smaller site in Staffordshire.
Worldwide, one in five tractors is powered by a Perkins engine. The French truck manufacturer ACMAT uses Perkins engines exclusively. Perkins engines are widely used in marine applications (Volvo Penta uses marinised Perkins engines for its widely-selling range of yacht powerplants), and in diesel generator sets.

Contents

1 History 

1.1 Massey-Ferguson
1.2 Caterpillar
2 Products
3 Sponsorship
4 See also
5 References
6 External links 

//

 History
F. Perkins Ltd. was formed on 7 June 1932 in Peterborough, England by Frank Perkins, who had worked with Charles Chapman at an engineering firm; on founding his own company, Perkins brought Chapman in as technical director and the pair created a high-speed, lightweight diesel engine, producing 35 of them in 1933 (sold to truck company Commer). Sales were strong and by the time of World War II the company made two series of engines, P4 and P6. After the war, the company went public, and licensed its designs to numerous foreign companies for local manufacturing and sale.[1]

 Massey-Ferguson
The company was sold to Massey-Ferguson Ltd. in 1959 and later became part of LucasVarity plc; development continued and Perkins updated its engines to meet stricter emissions rules, while developing new series for power generation and forklift trucks. In 1994, Perkins built its 15 millionth engine and signed agreements to supply Caterpillar and NACCO, the world's largest lift truck maker.

 Caterpillar
Caterpillar purchased the Perkins Engines Company from LucasVarity in 1998 for US $1.35 billion, creating what they claimed was the world's largest diesel engine manufacturer; Caterpillar had been one of Perkins' customers. Since then, Perkins has built a new factory in Georgia (U.S.) to produce its 400 series, and a new factory in Brazil. Perkins currently claims to be the leading supplier of engines in the under-2,000 kW market[2]

 Products
Perkins engines have been made for diesel, industrial, and power generation use, but two engines stand out among the general public for their automotive applications.
Perkins' 1.6 litre (99 cubic inch) P4C engine, producing 45 or 60hp (45kW), was extremely popular in Europe and Israel for taxis and commercially driven cars during the 1950s and early 1960s; many cars, including American imports, were retrofitted with these engines for taxi use, with kits made by Hunter NV of Belgium. Perkins engines were also used as standard factory equipment in Jeeps and Dodge trucks in the United States in the 1960s. They also continued to be popular in European trucks from their original customer, Commer and other companies.[1]
The Perkins 6.354 medium duty engine was designed to be compact enough to replace gasoline V8 engines in trucks, despite its in-line six-cylinder design. Producing 112horsepower (84kW) in early years (later rising to 120 hp), it had a small jackshaft driven by the timing gears for the auxiliary drive, with the oil pump driven by a quill shaft so it could run auxiliary equipment at engine speed with simple couplings. It used a low camshaft so the timing case could be smaller, allowing space for the water pump. This engine had a one-inch smaller bore than the P6 and R6 that preceded it, also to make it more compact, lengthwise. It had direct fuel injection, adding a chamber in the piston crown rather than in the head, so that there was more power and better mileage; port casting was made more precise, and a new CAV pump and injectors were used to reduce pollution. A turbocharged version was denoted by a leading T, and with air-to-air charge cooling, it output 150hp (110kW). The engine was not popular in the United States, where its uses were not as anticipated, leading to reliability issues, but it became a standby in Europe, appearing in (among other vehicles) the Dodge 100 trucks. A bored version of 372 cubic inches (6.372) was produced later.
After acquiring Rolls-Royce Diesels of Shrewsbury in the 1980s, Perkins continued to supply British Railways with engines for its diesel multiple units.

 Sponsorship
The company sponsors the Team Bath Racing team in the UK Formula Student competition.

 See also

Frank Perkins
List of Perkins engines 

 References

^ a b "Perkins diesel engines and the Perkins Ltd. company". http://www.allpar.com/mopar/perkins.html. Retrieved on 2008-05-16.
^ "Perkins Timeline". http://www.perkins.com/cda/layout?m=96906&x=7. Retrieved on 2008-05-16. 

 External links

Perkins Engines Company
History of Perkins Engines
UK Caterpillar site 

Categories: Engine manufacturers | Electrical generation engine manufacturers | Marine engine manufacturers | Companies established in 1932 | Peterborough | Companies based in Cambridgeshire | Caterpillar Inc. | Companies based in Peterborough

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Compression ratio

Wednesday, March 25th, 2009

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For compression ratio in data compression, see data compression ratio.
The compression ratio of an internal-combustion engine or external combustion engine is a value that represents the ratio of the volume of its combustion chamber; from its largest capacity to its smallest capacity. It is a fundamental specification for many common combustion engines.
In a piston engine it is the ratio between the volume of the cylinder and combustion chamber when the piston is at the bottom of its stroke, and the volume of the combustion chamber when the piston is at the top of its stroke.
Picture a cylinder with the piston at the bottom of its stroke containing 1000 cc of air. When the piston has moved up to the top of its stroke inside the cylinder, and the remaining volume inside the head or combustion chamber has been reduced to 100 cc, then the compression ratio would be proportionally described as 1000:100, or with fractional reduction, a 10:1 compression ratio.
A high compression ratio is desirable because it allows an engine to extract more mechanical energy from a given mass of air-fuel mixture due to its higher thermal efficiency. High ratios place the available oxygen and fuel molecules into a reduced space along with the adiabatic heat of compression - causing better mixing and evaporation of the fuel droplets. Thus they allow increased power at the moment of ignition and the extraction of more useful work from that power by expanding the hot gas to a greater degree.
Higher compression ratios will however make gasoline engines subject to engine knocking, also known as detonation and this can reduce an engine's efficiency or even physically damage it.
Diesel engines on the other hand operate on the principle of compression ignition, so that a fuel which resists autoignition will cause late ignition which will also lead to engine knock.

Contents

1 Formula
2 Typical compression ratios 

2.1 Petrol/gasoline engine
2.2 Petrol/gasoline engine with pressure-charging
2.3 Petrol/gasoline engine for racing
2.4 Gas-fuelled engine
2.5 Diesel engine
3 Fault finding and diagnosis
4 Saab Variable Compression engine
5 Variable Compression Ratio (VCR) Engines
6 Dynamic Compression Ratio
7 Compression ratio versus overall pressure ratio
8 See also
9 External links 

//

 Formula
The ratio is calculated by the following formula:

, where
b = cylinder bore (diameter)
s = piston stroke length
Vc = volume of the combustion chamber (including head gasket). This is the minimum volume of the space into which the fuel and air is compressed, prior to ignition. Because of the complex shape of this space, it is usually measured directly rather than calculated. 

 Typical compression ratios

 Petrol/gasoline engine
Due to pinging (detonation), the CR in a gasoline/petrol powered engine will usually not be much higher than 10:1, although some production automotive engines built for high-performance from 1955-1972 had compression ratios as high as 12.5:1, which could run safely on the high-octane leaded gasoline then available.
A technique used to prevent the onset of knock is the high "swirl" engine that forces the intake charge to adopt a very fast circular rotation in the cylinder during compression that provides quicker and more complete combustion. Recently, with the addition of variable valve timing and knock sensors to delay ignition timing, it is possible to manufacture gasoline engines with compression ratios of over 11:1 that can use 87 MON (octane rating) fuel.
In engines with a 'ping' or 'knock' sensor and an electronic control unit, the CR can be as high as 13:1 (2005 BMW K1200S). In 1981, Jaguar released a cylinder head that allowed up to 14:1 compression; but settled for 12.5:1 in production cars. The cylinder head design was known as the "may fireball" head.

 Petrol/gasoline engine with pressure-charging
In a turbocharged or supercharged gasoline engine, the CR is customarily built at 9:1 or lower.

 Petrol/gasoline engine for racing
Motorcycle racing engines can use compression ratios as high as 14:1, and it is not uncommon to find motorcycles with compression ratios above 12.0:1 designed for 86 or 87 octane fuel.
Racing engines burning methanol and ethanol often exceed a CR of 15:1. Consumers may note that "gasohol", or 90% gasoline with 10% ethanol gives a higher octane rating (knock suppression).

 Gas-fuelled engine
In engines running exclusively on LPG or CNG, the CR may be higher, due to the higher octane rating of these fuels.

 Diesel engine
In an auto-ignition diesel engine, (no electrical sparking plug--the hot air of compression lights the injected fuel) the CR will customarily exceed 14:1. Ratios over 22:1 are common. The appropriate compression ratio depends on the design of the cylinder head. The figure is usually between 14:1 and 16:1 for indirect injection engines and between 18:1 and 20:1 for direct injection engines.

 Fault finding and diagnosis
Measuring the compression pressure of an engine, with a pressure gauge connected to the spark plug opening, gives an indication of the engine's state and quality. There is, however, no formula to calculate compression ratio based on cylinder pressure.
If the nominal compression ratio of an engine is given, the pre-ignition cylinder pressure can be estimated using the following relationship:

where p0 is the cylinder pressure at bottom dead center (BDC) which is usually at 1 atm, Cr is the compression ratio, and ? is the ratio of specific heats of the working fluid, which is about 1.4 for air, and 1.3 for methane-air mixture.
For example, if an engine running on gasoline has a compression ratio is 10:1, the cylinder pressure at top dead center (TDC) is

This figure, however, will also depend on cam (i.e. valve) timing. Generally, cylinder pressure for common automotive designs should at least equal 10 bar, or, roughly estimated in pounds per square inch (psi) as between 15 and 20 times the compression ratio, or in this case between 150 psi and 200 psi, depending on cam timing. Purpose-built racing engines, stationary engines etc. will return figures outside this range.
Factors including late intake valve closure (relatively speaking for camshaft profiles outside of typical production car range, but not necessarily into the realm of competition engines) can produce a misleadingly low figure from this test. Excessive connecting rod clearance, combined with extremely high oil pump output (rare but not impossible) can sling enough oil to coat the cylinder walls with enough oil to facilitate reasonable piston ring seal artificially give a misleadingly high figure, on engines with compromised ring seal.
This can actually be used to some slight advantage. If a compression test does give a low figure, and it has been determined it is not due to intake valve closure/camshaft characteristics, then one can differentiate between the cause being valve/seat seal issues and ring seal by squirting engine oil into the spark plug orifice, in a quantity sufficient to disperse across the piston crown and the circumference of the top ring land, and thereby effect the mentioned seal. If a second compression test is performed shortly thereafter, and the new reading is much higher, it would be the ring seal that is problematic, whereas if the compression test pressure observed remains low, it is a valve sealing (or more rarely head gasket, or breakthrough piston or rarer still cylinder wall damage) issue.
If there is a significant (> 10%) difference between cylinders, that may be an indication that valves or cylinder head gaskets are leaking, piston rings are worn or that the block is cracked.
If a problem is suspected then a more comprehensive test using a leak-down tester can locate the leak.

 Saab Variable Compression engine
Because cylinder bore diameter, piston stroke length and combustion chamber volume are almost always constant, the compression ratio for a given engine is almost always constant, until engine wear takes its toll.
One exception is the experimental Saab Variable Compression engine (SVC). This engine, designed by Saab Automobile, uses a technique that dynamically alters the volume of the combustion chamber (Vc), which, via the above equation, changes the compression ratio (CR).
To alter Vc, the SVC 'lowers' the cylinder head closer to the crankshaft. It does this by replacing the typical one-part engine block with a two-part unit, with the crankshaft in the lower block and the cylinders in the upper portion. The two blocks are hinged together at one side (imagine a book, lying flat on a table, with the front cover held an inch or so above the title page). By pivoting the upper block around the hinge point, the Vc (imagine the air between the front cover of the book and the title page) can be modified. In practice, the SVC adjusts the upper block through a small range of motion, using a hydraulic actuator.

 Variable Compression Ratio (VCR) Engines
The SAAB SVC is an advanced and workable addition to the world of VCR engines, the first being built and tested by Harry Ricardo in the 1920s. This work led to him devising the octane rating system that is still in use today. SAAB has recently been involved in working with the 'Office of Advanced Automotive Technologies', to produce a modern petrol VCR engine that showed an efficiency comparable with that of a Diesel. Many companies have been carrying out their own research in to VCR Engines, including Nissan, Volvo, PSA/Peugeot-Citro?n and Renault but so far with no publicly demonstrated results.
The Atkinson cycle engine was one of the first attempts at variable compression. Since the compression ratio is the ratio between dynamic and static volumes of the combustion chamber the Atkinson cycle's method of increasing the length of the powerstroke compared to the intake stroke ultimately altered the compression ratio at different stages of the cycle.

 Dynamic Compression Ratio
The calculated compression ratio, as given above, presumes that the cylinder is sealed at the bottom of the stroke (bottom dead centre - BDC), and that the volume compressed is the actual volume.
However: intake valve closure (sealing the cylinder) always takes place after BDC, which causes some of the intake charge to be compressed backwards out of the cylinder by the rising piston at very low speeds; only the percentage of the stroke after intake valve closure is compressed. This "corrected" compression ratio is commonly called the "dynamic compression ratio".
This ratio is higher with more conservative (i.e., earlier, soon after BDC) intake cam timing, and lower with more radical (i.e., later, long after BDC) intake cam timing, but always lower than the static or "nominal" compression ratio.
The actual position of the piston can be determined by trigonometry, using the stroke length and the connecting rod length (measured between centers). The absolute cylinder pressure is the result of an exponent of the dynamic compression ratio. This exponent is a polytropic value for the ratio of variable heats for air and similar gases at the temperatures present. This compensates for the temperature rise caused by compression, as well as heat lost to the cylinder. Under ideal (adiabatic) conditions, the exponent would be 1.4, but a lower value, generally between 1.2 and 1.3 is used, since the amount of heat lost will vary among engines based on design, size and materials used, but provides useful results for purposes of comparison. For example, if the static compression ratio is 10:1, and the dynamic compression ratio is 7.5:1, a useful value for cylinder pressure would be (7.5)^1.3 � atmospheric pressure, or 13.7 bar. (� 14.7 psi at sea level = 201.8 psi. The pressure shown on a gauge would be the absolute pressure less atmospheric pressure, or 187.1 psi.)
The two corrections for dynamic compression ratio affect cylinder pressure in opposite directions, but not in equal strength. An engine with high static compression ratio and late intake valve closure will have a DCR similar to an engine with lower compression but earlier intake valve closure.
Additionally, the cylinder pressure developed when an engine is running will be higher than that shown in a compression test for several reasons.

The much higher velocity of a piston when an engine is running versus cranking allows less time for pressure to bleed past the piston rings into the crankcase. 

a running engine is coating the cylinder walls with much more oil than an engine that is being cranked at low RPM, which helps the seal. 

the higher temperature of the cylinder will create higher pressures when running vs. a static test, even a test performed with the engine near operating temperature. 

A running engine does not stop taking air & fuel into the cylinder when the piston reaches BDC; The mixture that is rushing into the cylinder during the downstroke develops momentum and continues briefly after the vacuum ceases (in the same respect that rapidly opening a door will create a draft that continues after movement of the door ceases). This is called scavenging. Intake and cylinder head designs determine how effectively an engine scavenges. 

 Compression ratio versus overall pressure ratio
Compression ratio and overall pressure ratio are interrelated as follows:

Compression ratio
1:1
3:1
5:1
10:1
15:1
20:1
25:1
35:1

Pressure ratio
1:1
2:1
10:1
22:1
40:1
56:1
75:1
110:1
The reason for this difference is that compression ratio is defined via the volume reduction,

,
Pressure ratio is defined as the pressure increase

.
From the combined gas law we get:

Since T2 is much higher than T1 (compressing gases puts work into them, i.e. heats them up), CR is much lower than PR.

 See also

Overall pressure ratio - a closely related ratio for jet engines 

 External links

SVC
Cam Timing vs. Compression Ratio Analysis 

Categories: Piston engines | Engine technology | Saab engines | Engineering ratios

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Steam shower

Wednesday, March 25th, 2009

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This article does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unverifiable material may be challenged and removed. (August 2007)
A steam shower is a type of bathing where a humidifying steam generator produces water vapor that is dispersed around a person's body. These types of showers are becoming increasingly popular in many countries.[citation needed]. A steam shower is essentially a steam room that offers the typical features of a bathroom shower.
Steam showers are generally found in self-contained enclosures that prevent the water vapour from escaping into the main part of the bathroom, avoiding damage to drywall, paint, or wallpaper. Steam showers are available in a variety of materials, including but not limited to tile, acrylic, fiberglass, stone, and wood.
It is possible to convert an existing bathroom shower into a steam shower by adding a steam generator. The steam generator will produce steam and water (a byproduct), which must be connected to a drain below the shower, or designed to drain into the base of the shower.
Most steam shower rooms are sold as stand-alone shower units with between 6 and 32 jets located above the head, along the back or behind the lower legs. Modern steam showers may provide additional features such as foot massagers, ceiling rain showers, television, radios, telephones, audio input from an MP3 or CD player, chromatherapy or aromatherapy.
Steam showers are often available in gyms, but have also become a more common bathroom fixture in recent years, primarily due to falling costs.
The water vapour produced by these shower units is often referred to in common speech as "steam," but this is a misnomer. In physical chemistry and in engineering, steam is a completely invisible gas and would result in serious burns if applied in the shower.
A Steam Shower can use Solar Thermal technology and lessen the electric bill drastically by heating the water with the sun.

 See also

Banya (sauna) -- A Russian steambath
Hammam -- A Turkish steambath
Steam room --Traditional
Sauna
Solar hot water 

Categories: Bathing | Water in gas
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PCV valve

Wednesday, March 25th, 2009

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The Positive Crankcase Ventilation valve, or PCV valve, is a one-way valve that ensures continual evacuation of gases from inside a gasoline internal combustion engine's crankcase.

Contents

1 Explanation
2 History
3 PCV system
4 PCV valve
5 Operation 

//

 Explanation
As an engine runs, high-pressure gases are contained within the combustion chamber and prevented from passing into the crankcase (containing the crankshaft and other parts) between the side of the piston and the cylinder bore by piston rings which seal against the cylinder. However, some amount of gas always leaks past the piston rings into the crankcase. This amount is very small in a new or properly rebuilt engine, provided that the piston rings and cylinder walls are correctly "broken in", and increases as the engine wears. Scratches on the cylinder walls or piston rings, such as those caused by foreign objects entering the engine, can cause large amounts of leakage. This leaked gas is known as blow-by because the pressure within the cylinders blows it by the piston rings. If this blow-by gas could not escape then pressure would build up within the crankcase.
Before the invention of Crankcase Ventilation in 1928 the engine oil seals were designed to withstand this pressure, oil leaking to the ground was accepted and the dipstick was screwed in. The hydrocarbon rich gas would then diffuse through the oil in the seals into the atmosphere. It is therefore an emissions requirement as well as a functional necessity that the crankcase has a ventilation system. This must maintain the crankcase at slightly less than atmospheric pressure and recycle the blow-by gas back into the engine intake. However, due to the constant circulation of the oil within the engine, along with the high speed movement of the crankshaft, an oil mist is also passed through the PCV system and into the intake. The oil is then either burnt during combustion or settles along the intake tract, causing a gradual build-up of residue inside the inlet path. For this reason many engine tuners choose to replace the PCV system with an oil catch can and breather filter which vents the blow-by gases directly to atmosphere and retains the oil in a small tank (or returns it to the sump), although this technically fails to meet most engine emission legislation.

 History
Prior to the early 1960s, automobile gasoline engines vented combustion gases directly to the atmosphere through a simple vent tube. Frequently this consisted of a pipe (the "road draft tube") that extended out from the crankcase down to the bottom of the engine compartment. The bottom of the pipe was open to the atmosphere, and was placed such that when the car was in motion a slight vacuum would be hopefully obtained, helping to extract combustion gases as they collected in the crankcase. The oil mist would also be discharged, resulting in an oily film being deposited in the middle of each travel lane on heavily-used roads. The system was not positive though, as gases could travel both ways, or not move at all, dependent on conditions. Most modern diesel engines still use this type of system to dispose of crankcase fumes. During World War II however, a different type of crankcase ventilation had to be invented to allow tank engines to operate during deep fording operations, where the normal draft tube ventilator would have allowed water to enter the crankcase and destroy the engine. The PCV system and its control valve were invented to meet this need but the need for it on automobiles was not recognized.
In 1952, Professor A. J. Haagen-Smit, of the California Institute of Technology at Pasadena, postulated that unburned hydrocarbons were a primary constituent of smog, and that gasoline powered automobiles were a major source of those hydrocarbons. After some investigation by the GM Research Laboratory (Dr. LLoyd L. Withrow) it was discovered in 1958 that the road draft tube was a major source, about half, of the hydrocarbons coming from the automobile. GM's Cadillac Division, which had built many tanks during WWII, recognized that the simple PCV valve could be used to become the first major reduction in automotive hydrocarbon emissions. After confirming the PCV valves' effectiveness at hydrocarbon reduction, GM offered the PCV solution to the entire U.S. automobile industry, royalty free, through its trade association, the Automobile Manufacturers Association (AMA). In the absence of any legislated requirement, the AMA members agreed to put it on all California cars voluntarily in the early 1960s, with national application following one year later.
Following its introduction into production, several years later the PCV became the subject of a Federal grand jury investigation in 1967, when it was alleged by some industry critics that the AMA was conspiring to keep several such smog reduction devices like the PCV on the shelf to delay smog control. After eighteen months of investigation by U.S. Attorney Samuel Flatow, the grand jury returned a "no-bill" decision, clearing the AMA, but resulting in a "Consent Decree" that all U.S. automobile companies agreed not to work jointly on smog control activities for a period of ten years.

 PCV system
The PCV valve is only one part of the PCV system, which is essentially a variable and calibrated air leak, whereby the engine returns its crankcase combustion gases. Instead of the gases being vented to the atmosphere, gases are fed back into the intake manifold, to re-enter the combustion chamber as part of a fresh charge of air and fuel. The PCV system is not a classical "vacuum leak." All the air collected by the air cleaner (and metered by the mass air flow sensor, on a fuel injected engine) goes through the intake manifold. The PCV system just diverts a small percentage of this air via the breather to the crankcase before allowing it to be drawn back in to the intake tract again. It is an "open system" in that fresh exterior air is continuously used to flush contaminants from the crankcase and into the combustion chamber.
The system relies on the fact that, while the engine is running, the intake manifold's air pressure is always less than crankcase air pressure. The lower pressure of the intake manifold draws air towards it, pulling air from the breather through the crankcase (where it dilutes and mixes with combustion gases), through the PCV valve, and into the intake manifold.
The PCV system consists of the breather tube and the PCV valve. The breather tube connects the crankcase to a clean source of fresh air, such as the air cleaner body. Usually, clean air from the air cleaner flows in to this tube and in to the engine after passing through a screen, baffle, or other simple system to arrest a flame front, to prevent a potentially explosive atmosphere within the engine crank case from being ignited from a back-fire in to the intake manifold. The baffle, filter, or screen also traps oil mist, and keeps it inside the engine.
Once inside the engine, the air circulates around the interior of the engine, picking up and clearing away combustion byproduct gases, including a large amount of water vapor, then exits through a simple baffle, screen or mesh to trap oil droplets before being drawn out through the PCV valve, and into the intake manifold.

 PCV valve

PCV valve on Ford Taunus V4 engine in a Saab 96, between left valve cover and intermediate flange on intake manifold
The PCV valve connects the crankcase to the intake manifold from a location more-or-less opposite the breather connection. Typical locations include the opposite valve cover that the breather tube connects to on a V engine. A typical location is the valve cover(s), although some engines place the valve in locations far from the valve cover. The valve is simple, but actually performs a complicated control function. An internal restrictor (generally a cone or ball) is held in "normal" (engine off, zero vacuum) position with a light spring, exposing the full size of the PCV opening to the intake manifold. With the engine running, the tapered end of the cone is drawn towards the opening in the PCV valve, restricting the opening proportionate to the level of engine vacuum vs. spring tension. At idle, the intake manifold vacuum is near maximum. It is at this time the least amount of blow by is actually occurring, so the PCV valve provides the largest amount of (but not complete) restriction. As engine load increases, vacuum on the valve decreases proportionally and blow by increases proportionally. Sensing a lower level of vacuum, the spring returns the cone to the "open" position to allow more air flow. At full throttle, there is nearly zero vacuum. At this point the PCV valve is nearly useless, and most combustion gases escape via the "breather tube" where they are then drawn in to the engine's intake manifold anyway.

 Operation
Should the intake manifold's pressure be higher than that of the crankcase (which can happen in a turbo charged engine or under certain conditions, such as an intake backfire), the PCV valve closes to prevent reversal of the exhausted air back into the crankcase again. Positive is not a synonym for 'one way', but for 'real', 'definite', 'incontestable' i.e. one of its other meanings. It simply means there is a constant and definite flow of air through the system, as compared to the hit-and-miss road draught system used previously, in which air may flow in either direction or not at all. In many cases PCV valves were only used for a few years, the function being taken over by a port on constant depression carburettors such as the SU. This has no moving parts or diaphragm to jam, block or rip like many PCV valves. It also doesn't have a 'one-way' function but the lack of it was never a problem in intake backfire.
It is critical that the parts of the PCV system be kept clean and open, otherwise air flow will be insufficient. A plugged or malfunctioning PCV system will eventually damage an engine. PCV problems are primarily due to neglect or poor maintenance, typically engine oil change intervals that are inadequate for the engine's driving conditions. A poorly-maintained engine's PCV system will eventually become contaminated with sludge, causing serious problems. If the engine's lubricating oil is changed with adequate frequency, the PCV system will remain clear practically for the life of the engine. However, since the valve is operating continuously as one operates the vehicle, it will fail over time. Typical maintenance schedules for gasoline engines include PCV valve replacement whenever the air filter or spark plugs are replaced. The long life of the valve despite the harsh operating environment is due to the trace amount of oil droplets suspended in the air that flows through the valve that keep it lubricated.
Not all gasoline engines have PCV valves. Engines not subject to emission controls, such as certain off-road engines, retain road draft tubes. Dragsters use a scavenger system and venturi tube in the exhaust to draw out combustion gases and maintain a small amount of vacuum in the crankcase to prevent oil leaks on to the race track. Small gasoline two stroke engines use the crank case to compress incoming air. All blow by in these engines is burned in the regular flow of air and fuel through the engine. Many small four-cycle engines such as lawn mower engines and small gasoline generators, simply use a draft tube connected to the intake, between the air filter and carburetor, to route all blow by back into the intake mixture. The higher operating temperature of these small engines has a side effect of preventing large amounts of water vapor and light hydrocarbons from condensing in the engine oil.
 [1] - PCV images

Categories: Auto parts | Engine valves | Engine technology | Pollution control technologies

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