Vinylidene chloride.

Cover of: Vinylidene chloride. |

Published by World Health Organization in Geneva .

Written in English

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  • Dichloroethylene -- Toxicology.,
  • Halocarbons -- Toxicology.,
  • Dichloroethylenes.,
  • Hydrocarbons, Chlorinated.

Edition Notes

Book details

SeriesEnvironmental health criteria -- 100.
ContributionsWorld Health Organization., United Nations Environment Programme., International Labour Organisation., International Program on Chemical Safety.
The Physical Object
Pagination187 p. :
Number of Pages187
ID Numbers
Open LibraryOL18006888M
ISBN 109241543000

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Vinylidene chloride is used as an intermediate in chemical synthesis and to produce polyvinylidene chloride Vinylidene chloride. book. The primary acute (short-term) effects in humans from vinylidene chloride exposure are on the central nervous system (CNS), including CNS depression and symptoms of inebriation, convulsions, spasms, and unconsciousness at high concentrations.

Polyvinylidene chloride (PVDC) resin, the structure of which is shown in Fig. is usually a copolymer of vinylidene chloride with vinyl chloride or other monomers. Dow Plastics vinyl chloride and vinylidene chloride, Saran™, is usually supplied as a white, free flowing powder.

PVDC has a. Suggested Citation:"Vinylidene Chloride."National Research Council. Emergency and Continuous Exposure Limits for Selected Airborne Contaminants: Volume 2. Vinylidene Chloride (1,1-Dichloroethylene) Hazard Summary Vinylidene chloride is used as an intermediate in chemical synthesis and to produce polyvinylidene chloride copolymers.

The primary acute (short-term) effects in humans from vinylidene chloride exposure are on. Vinylidene chloride definition is - a low-boiling flammable liquid compound CH2=CCl2 prepared usually from trichloroethane and used in making saran by polymerization; 1,1-dichloro-ethylene. Polyvinylidene chloride or Polyvinylidene dichloride (PVDC) is a homopolymer of vinylidene chloride.

Ralph Wiley accidentally discovered polyvinylidene chloride in He, then, was a college Vinylidene chloride. book who worked part-time at Dow Chemical lab as a dishwasher.

While cleaning laboratory glassware, he came across a vial he could not scrub Number: In another one-step process, [8] a mixture of vinylidene chloride and hydrofluoric acid is heated to °C°C in the presence of oxygen and a catalyst.

Aluminum fluoride, alone or in combination with a transition metal such as cobalt, chromium, nickel, zinc or their combinations, is.

Vinylidene chloride. London: Health and Safety Executive, (OCoLC) Material Type: Government publication: Document Type: Book: All Authors / Contributors: R J Fielder; E A Dale; S D Williams; Great Britain.

Health and Safety Executive. Vinylidene chloride (CH 2 =CCl 2), a clear, colourless, toxic liquid, is obtained from trichloroethane (CH 2 =CHCl 3) through the dehydrochlorination (removal of hydrogen chloride [HCl]) of that compound by alkali treatment.

For processing into PVDC, the liquid is suspended in water as fine droplets or treated with soaplike surfactants and dispersed in water as an emulsion of small particles. Recycling Biaxially Oriented Polypropylene Films Coated with Vinylidene Chloride Polymers, Polymers, Laminations & Coatings Conference Proceedings.

COVID Resources. Reliable information about the coronavirus (COVID) is available from the World Health Organization (current situation, international travel).Numerous and frequently-updated resource results are available from this ’s WebJunction has pulled together information and resources to assist library staff as they consider how to handle coronavirus.

Polyvinylidene chloride definition is - a polymer of vinylidene chloride: such as. Love words. You must — there are overwords in our free online dictionary, but you are looking for one that’s only in the Merriam-Webster Unabridged Dictionary.

Start your free trial today and get unlimited access to America's largest dictionary, with. More thanwords that aren't in our. vinylidene chloride[vī′nilə‚dēn ′klȯr‚īd] (organic chemistry) CH2:CCl2 A colorless, flammable, explosive liquid, insoluble in water; boils at 37°C; used to make polymers copolymerized with vinyl chloride or acrylonitrile (Saran).

Vinylidene Chloride (1,1-dichloroethylene, CH2= CC12), a colorless liquid that has an odor resembling that of. vinylidene chloride by inhalation at concentrations of 0, or 25 ppm, 6 hours and 10 minutes per day, 5 days per week for up to weeks.

The lifetime average daily doses of vinylidene chloride administered in the studies were calculated to be: 0,10, and 20 mg/kg-day in male mice and 0, and 20 mg/kg-day in female Size: KB. Vinylidene chloride. Related Pages. Synonyms & Trade Names 1,1-DCE, 1,1-Dichloroethene, 1,1-Dichloroethylene, VDC, Vinylidene chloride monomer, Vinylidene dichloride CAS No.

RTECS No. KV DOT ID & Guide. P(inhibited) Formula. CH₂=CCl₂. Vinylidene Chloride. Our line of Vinylidene Chloride offers the reliability and performance you need, backed by the local customer support Only Olin can provide, virtually anywhere in the world.

(—CH 2 — CC1 2 —)n, a linear and thermoplastic polymer of vinylidene chloride. Polyvinylidene chloride is a white plastic with a molecular weight of up toIts degree of crystallinity is up to 50 percent and its density at 30°C is g/cm Physiologically harmless and incombustible, polyvinylidene chloride is rather strong, with a tensile strength of 40 meganew-tons per sq.

Vinylidene chloride, also called 1,1-dichloroethylene, a colourless, dense, toxic, volatile, flammable liquid belonging to the family of organic halogen compounds, used principally in combination with vinyl chloride, acrylonitrile, or methyl methacrylate for the manufacture of a class of plastics called dene chloride is also used as a starting material for making methylchloroform.

Summary: Evaluates the environmental hazards and risks to human health posed by the production and use of vinylidene chloride. Vinylidene chloride/vinyl chloride copolymers are used for the packaging of foods, as metal coatings in storage tanks, building structures.

IARC published on its website a list entitled “Agents Classified by the IARC Monographs, Volumes 1 - " (IARC, ). IARC concludes that vinylidene chloride is classified in Group 2B (“possibly carcinogenic to humans”), and that there is sufficient evidence of carcinogenicity in animals for vinylidene chloride (Grosse et al., ).

See Also: Toxicological Abbreviations Vinylidene chloride (EHC) Vinylidene chloride ( ) Vinylidene Chloride (IARC Summary & Evaluation, Vol ).

This is the amount of vinylidene chloride which gave a chromatographic peak large enough to distinguish it from the leading edge of a contaminant peak present in the CS 2. (Section ) The detection limit of the overall procedure is µg per sample ( ppm or mg/m 3).boiling point: °C ( mm).

Vinyl and Vinylidene Chlorides Poly(vinyl chloride) is often highly plasticized to improve rheology for melt processing. It is highly susceptible to UV and high-temperature degradation and stabilizers (see Stabilizers in the Polymer Additives section) are commonly added.

for the analysis of 36 samples over the range 12 to 85 µg vinylidene chloride per sample. Desorption efficiency was determined to be 80% for a loading of 7 µg vinylidene chloride at a vinylidene chloride concentration of 10 mg/m3 and high relative humidity; the breakthrough volume was L when sampling at L/min from this atmosphere.

There is disclosed expandable vinylidene chloride-based resin particles comprising parts by weight of a non-crystalline vinylidene chloride-based resin composition and 1 to 40 parts by weight of a volatile organic blowing agent or a composition thereof, said resin composition consisting of a tetrahydrofuran-soluble component [A] which is a random copolymer having a weight-average molecular Cited by: Cite this entry as: () Poly(vinylidene fluoride).

In: Gooch J.W. (eds) Encyclopedic Dictionary of Polymers. Springer, New York, A thermoplastic polymer that is commonly called saran. Polyvinylidene chloride forms films that are impermeable to vapors, moisture, and oxygen. It is most often used as a barrier film for packaging.

In an eco-friendly step, the brand name 'Saran Wrap' product changed formulations in to polyethylene film. See also saran y: n CH 2:CCl 2.A monomer.

Bp, 37°C. A colorless, volatile liquid that is produced by the dehydrochlorination of 1,1,2-trichloroethane. It is a monomer for Polyvinylidene Chloride and is a comonomer with vinyl chloride (see Saran) and other monomers such as known as 1,1-Dichloroethylene.

Open image in new window. emit vinylidene chloride to the air. This section discusses the production of vinylidene chloride, its use as an industrial feedstock, and processes which produce vinylidene chloride as a byproduct. For each major industrial source category described in Section 4, example process.

Search term: "vinylidene chloride" Compare Products: Select up to 4 products. *Please select more than one item to compare. 18 matches found for vinylidene chloride. Advanced Search | Structure Search. 1,1-Dichloroethylene. 3 Product Results. Peroxidizable monomer, such as VINYLIDENE CHLORIDE, may initiate exothermic polymerization of the bulk material [Bretherick p.].

Mixing vinylidene chloride in equal molar portions in a closed container with any of the following substances caused the temperature and pressure to increase: chlorosulfonic acid, nitric acid, or oleum. Measured steady state levels of vinylidene fluoride in blood of mice increased with increasing exposure concn.

For both and ppm vinylidene fluoride exposures, the experimentally determined data fell within the 95% confidence interval predicted by the physiological model. Vinylidene definition: of, consisting of, or containing the group CH 2:C | Meaning, pronunciation, translations and examples.

Vinylidene chloride was not detected in any of the raw water samples, and only one finished water sample collected during the summer months (Aug.- Sept.) showed a mean concentration of less than 1 }ig/l and a maximum concentra- tion of 20 p.g/1 for vinylidene chloride.

Exposure It can be concluded from the discussions in Section Impartial feasibility studies focused on vinylidene chloride copolymer manufacturing economics, showing CAPEX, OPEX, key process indicators and process diagrams. Know more at Define vinylidene.

vinylidene synonyms, vinylidene pronunciation, vinylidene translation, English dictionary definition of vinylidene. n of, consisting of, or containing the group CH2:C: a vinylidene group or radical; vinylidene chloride; a vinylidene resin.

Check out Polyvinylidene Chloride (PVDC) from ICL Phosphate Specialty Corrosion Inhibitors and Paint & Coating Additives. Product Info & Sales () Free Samples Distributor s Login Site Search. Renal cell carcinomas in vinylidene chloride-exposed male B6C3F1 mice are characterized by oxidative stress and TP53 pathway dysregulation.

Toxicol Pathol. Jan;44(1) TR (NIH Number: ) (Peer Review Approval 10/29/A). Vinylidene chloride is a versatile monomer used primarily for making Vinylidene chloride copolymers. These copolymers are mostly used in food packaging to provide a good barrier-to-mass transport.

Vinylidene Chloride Suppliers USA. Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods. Search for products or services, then visit the American suppliers website for prices, SDS or more information.

You can also view suppliers in Australia, NZ or the UK. Vinylidene chloride is used in the production of polyvinylidene chloride (PVDC) copolymers. PVDC was developed by Dow Chemical Company, and was at one point used in the production of the popular food wrap product, Saran Wrap.

PVDC has characteristics ideal for food packaging because it has low permeabiltiy to water vapor and gasses.Vinylidene chloride is a central nervous system depressant. Repeated exposure to low concentrations of vinylidene chloride may cause liver and renal dysfunction (Torkelson & Rowe, ).

Skin contact with vinylidene chloride causes irritation, which may be due partly to the presence of an inhibitor, hydroquinone monomethyl ether (Chivers, ).

InFile Size: 59KB.The infrared spectra of polyvinyl chloride, polyvinylidene chloride, and their copolymers have been analyzed with the help of group theory and of spectra in the extended range of 70 to cm.−1.

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