A new dual mass flywheel that acts like a harmonic balancer.

I have just had to replace a dual mass flywheel on my 2.0-litre Ford Focus after 51,000 miles.

You might also soon need a fresh dual mass flywheel replacement and particulate filter.

Reliable chain-cam engines, although a few clutch and dual mass flywheel problems have been reported.

Crank Failure: Related to age failures of the harmonic balancer, the vibration damped accessory drive pulley, or the dual mass flywheel.

The transmission used the skip-shift feature to conserve fuel during light loads by preventing drivers from using the second and third gears, and a dual mass flywheel to reduce "rattle" in no load conditions.

Getrag provided a six-speed manual transmission shared with the Mini Cooper S. This transmission was a twin layshaft design and included a dual mass flywheel to eliminate vibration and transmission noise.

Flynn also founded DMF Inc. which is a privately owned corporation.

These organic salts are soluble in polar organic solvents such as acetonitrile and dmf.

'I regret that we have had to take this step,' said DMF managing director Neil Friar.

DMF Championship winners:

This is carried out through a program that was developed in 1988, the DMF Artificial Reef Master Plan.

Pre-assignment of DMF Numbers (Category 3)

Between Flynn Energy Corp. and DMF Inc., the net income for both companies totaled $542 million.

DMF Comics and Beach Creative Studios will be working on a comic book series for Storm Hawks.

PDC in DMF (Corey and Schmidt)

DMF Inc. holds interest in 19 producing wells in Michigan, Oklahoma, Texas, and Louisiana.

DMF Chronic Toxicity Summary (PDF)

In 1999, seven DMF First class vehicles were converted to include Checked Luggage compartments, with a partition in the centre of the car.

C and dC bear acetyl protection, and G and dG are protected with 4-isopropylphenoxyacetyl (iPr-PAC) or dimethylformamidino (dmf) groups.

Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market.

Commonly used solvents are polar aprotic solvents such as THF, DMSO, Acetonitrile, DMF as well as in non-polar aprotic solvents such as toluene.

The most common oxidants are potassium permanganate (KMnO), Jones reagent, PDC in DMF, Heyns oxidation, ruthenium tetroxide (RuO) and TEMPO.

The primary use of dimethylformamide is as a solvent with low evaporation rate.

A classic example of a fluxional molecule is dimethylformamide.

When dissolved in dimethylformamide, its absorption maximum lies at about 442 nm.

The reaction with thionyl chloride may be catalyzed by dimethylformamide.

Spontaneous ignition can result from solution of sodium borohydride in dimethylformamide.

In this experiment the guests were the molecules already present in the reaction medium such as argon and dimethylformamide.

Although often abbreviated DMF, it should not be confused with dimethylformamide.

All drugs were dissolved in dimethylformamide to 2 mM solutions and stored in the dark at -20 C.

The newly formed 2-butenedioic acid derivative will react with dimethylformamide, forming a 2,3-quinolinedicarboxylic acid.

Industrial acetylene gas is, therefore, dissolved in dimethylformamide and stored in metal cylinders or bottles.

In the case of solution-based processing, typical solvents used include dimethylformamide as well as the more volatile butanone.

Tetraphenylbutatriene was reported synthesized in 1977 by homocoupling of 2,2-diphenyl-1,1,1-tribromoethane with elemental copper in dimethylformamide.

Protection: Tert-butyldiphenylsilyl chloride, imidazole, and dimethylformamide.

Salt efflorescences of calcium carbonate were treated by the application of a solution of dimethylformamide.

Note: Acetylene cylinders contain an inert packing material and are filled with a solvent such as acetone or dimethylformamide.

The synthesis is started by nucleophilic substitution of 1-bromopentane by triethyl sodiomethanetricarboxylate in dimethylformamide and benzene.

The choice of solvent or their ratio affects the reaction rate; in particular, higher content of dimethylformamide results in stronger oxidation.

It is highly soluble in dichloromethane, tetrahydrofuran, acetonitrile and dimethylformamide, but insoluble in water.

The most popular method uses dimethylformamide (DMF) as a solvent, and sometimes aniline is added to accelerate the reaction.

Dimethylformamide can be synthesized from methyl formate and dimethylamine or by reaction of dimethylamine with carbon monoxide.

Typical cryoprotectants include glycerol, DMSO and dimethylformamide.

In the initial enamine formation, dimethylamine (a gas) is displaced by pyrrolidine from the dimethylformamide dimethylacetal, producing a more reactive reagent.

The oxidation is usually carried out at ambient conditions, in nearly neutral pH conditions, in dimethylformamide or dichloromethane or their mixture.

The terminal aqua ligands on the trimetallic framework can be substituted with other ligands, such as pyridine and dimethylformamide.

NMF is closely related to other formamides, notably formamide and dimethylformamide (DMF).