비닐 플루오르화물

비닐 플루오르화물
비닐 플루오르화물 구조식 이미지
카스 번호:
75-02-5
한글명:
비닐 플루오르화물
동의어(한글):
비닐플루오라이드;비닐플루오르화물;플루오린화바이닐(플루오르화비닐);플루오린화바이닐(플루오르화비닐);비닐 플루오라이드
상품명:
VINYL FLUORIDE
동의어(영문):
Ethene, fluoro-;FLUOROETHYLENE;Fluoroethene;C2H3F;R-1141;FC-1141;inhibied;vinyl fluoro-ethen;ethene,fluro-
CBNumber:
CB0419082
분자식:
C2H3F
포뮬러 무게:
46.04
MOL 파일:
75-02-5.mol
MSDS 파일:
SDS

비닐 플루오르화물 속성

녹는점
-160,5°C
끓는 점
-72°C
밀도
0,615 g/cm3
굴절률
1.34
Henry's Law Constant
8.2×10-5 mol/(m3Pa) at 25℃, HSDB (2015)
CAS 데이터베이스
75-02-5(CAS DataBase Reference)
IARC
2A (Vol. Sup 7, 63, 97) 2008
EPA
Vinyl fluoride (75-02-5)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F
위험 카페고리 넘버 12-40
안전지침서 9-16-23-36/37/39
유엔번호(UN No.) UN 1860 (VINYL FLUORIDE, STABILIZED)
OEB D
OEL TWA: 1 ppm, Ceiling: 5 ppm [use 1910.1017]
위험 참고 사항 Flammable
TSCA TSCA listed
위험 등급 2.1
HS 번호 2903290000
유해 물질 데이터 75-02-5(Hazardous Substances Data)
중점관리물질 필터링 별표2-15
그림문자(GHS): Flame (GHS02)Health Hazard (GHS08)
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H220 극인화성 가스 인화성 가스 구분 1 위험 P210, P377, P381, P403
H280 고압가스; 가열시 폭발할 수 있음 고압가스 압축가스
액화가스
용존 가스
경고 P410+P403
H341 유전적인 결함을 일으킬 것으로 의심됨 (노출되어도 생식세포 유전독성을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 생식세포 변이원성 물질 구분 2 경고 P201,P202, P281, P308+P313, P405,P501
H350 암을 일으킬 수 있음 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 1A, 1B 위험
H373 장기간 또는 반복 노출되면 장기(또는, 영향을 받은 알려진 모든 장기를 명시)에 손상을 일으킬 수 있음 특정 표적장기 독성 - 반복 노출 구분 2 경고 P260, P314, P501
예방조치문구:
P201 사용 전 취급 설명서를 확보하시오.
P202 모든 안전 조치 문구를 읽고 이해하기 전에는 취급하지 마시오.
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P260 분진·흄·가스·미스트·증기·...·스프레이를 흡입하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
P314 불편함을 느끼면 의학적인 조치·조언을 구하시오.
P377 누출성 가스 화재 시 : 누출을 안전하게 막을 수 없다면, 불을 끄려하지 마시오.
P381 누출의 경우, 모든 점화원을 제거하시오.
P403 환기가 잘 되는 곳에 보관하시오.
P405 밀봉하여 저장하시오.
P410+P403 직사광선을 피하고 환기가 잘 되는 곳에 보관하시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
4
2 2

비닐 플루오르화물 C화학적 특성, 용도, 생산

개요

Vinyl fluoride (VF) was first synthesized by Frederic Swarts, a Belgian chemist in 1901, by the reaction between zinc and 1,1-difluoro-2-bromoethane. Modern preparation involves the reaction of acetylene and hydrogen fluoride (HF) in the presence of a mercury- or aluminum-based catalyst. The US Environmental Protection Agency (EPA) listed VF as a highproduction- volume chemical in 1990. According to National Toxicology Program (NTP), 2005, the annual production of VF in the United States was above 1 million pounds (454 000 kg) in 1990 and approximately 3.3 million pounds (1.5 million kg) in 2001.

화학적 성질

Vinyl fluoride is a colorless gas.

용도

Vinyl fluoride is used primarily in the production of polyvinyl fluoride and other fluoropolymers. Polymers of vinyl fluoride are resistant to weather and exhibit great strength, chemical inertness, and low permeability to air and water. Polyvinyl fluoride is laminated with aluminum, galvanized steel, and cellulose materials and is used as a protective surface for the exteriors of residential and commercial buildings. Polyvinyl fluoride laminated with various plastics has been used to cover walls, pipes, and electrical equipment and inside aircraft cabins (IARC 1995).

생산 방법

The first preparation of VF in the early 1900s was by reacting zinc with 1,1-difluoro-2-bromomethane.
VF was considered to be a high production volume chemical according to the U.S. Environmental Protection Agency with annual production exceeding 1million lb in 1990. In 2001, annual U.S. production was estimated approximately 3.3 million lb. In 1994, VF was produced by one company each in Japan and the United States. More recently, only one U.S. manufacturer of VF was identified . Information on European manufacturer is not available.
The modern production is by the addition of hydrogen fluoride to acetylene over a mercury- or aluminum-based catalyst.

제조 방법

Vinyl fluoride may be obtained from acetylene by either of the two following routes:

75-02-5 synthesis_1


In the first method, acetylene is heated with hydrogen fluoride in the presence of a catalyst of mercuric chloride on charcoal at about 40C to yield vinyl fluoride directly. In the second method, acetylene is treated with an excess of hydrogen fluoride to form difluoroethane which is then pyrolysed at about 700C in a platinum tube to give vinyl fluoride, which is separated by distillation under pressure.
Vinylidene fluoride is obtained from vinylidene chloride by the following route:

75-02-5 synthesis_2


In the first stage, vinylidene chloride undergoes addition with hydrogen chloride at about 30C and atmospheric pressure in the presence of a FriedelCrafts type catalyst. The resulting trichloroethane is then treated with hydrogen fluoride at about 180C and 3 MPa (30 atmospheres) in the presence of antimony pentachloride to give chlorodifluoroethane. Pyrolysis of this product yields vinylidene fluoride. Vinylidene fluoride is a gas, b.p. -84C.

일반 설명

A colorless gas with a faint ethereal odor. Shipped as a confined liquid under its vapor pressure. Any leak can either be liquid or vapor. Contact with the liquid can cause frostbite. Easily ignited. Vapors are heavier than air. Can asphyxiate by the displacement of air. Under prolonged exposure to fire or intense heat the containers may rupture violently and rocket.

공기와 물의 반응

Highly flammable, reacts with air to form peroxides

반응 프로필

VINYL FLUORIDE is light sensitive, peroxidizable monomer may initiate exothermic polymerization of the bulk material [Handling Chemicals Safely 1980. p. 958]. Sensitive to many oxidants.

건강위험

Inhalation of vapor causes slight intoxication, some shortness of breath. Liquid may cause frostbite of eyes or skin.

Safety Profile

Confirmed carcinogen. A poison. Mutation data reported. A very dangerous fire hazard. To fight fire, stop flow of gas. When heated to decomposition it emits toxic fumes of F-. See also FLUORIDES.

잠재적 노출

Vinyl fluoride’s primary use is as a chemical and polymer intermediate; used to make polyvinyl fluoride (Tedlar) film. Polyvinyl fluoride film is characterized by superior resistance to weather, high strength; and a high dielectric constant. It is used as a film laminate for building materials and in packaging electrical equipment. Polyvinyl fluoride film poses a hazard, so it is not recommended for food packaging. Polyvinyl fluoride evolves toxic fumes upon heating.

Carcinogenicity

Vinyl fluoride is reasonably anticipated to be a human carcinogenbased on sufficient evidence of carcinogenicity from studies in experimental animals.

환경귀착

VF is expected to exist solely as a gas in the ambient atmosphere. The gas-phase of VF is degraded in the atmosphere by reaction with photochemically produced hydroxyl radicals. The half-life for this reaction in air is estimated to be 3 days as calculated from its rate constant of 5.56 × 10-12 cm3 molecule sec--1 at 25°C. VF also reacts with atmospheric ozone, leading to its atmospheric degradation (estimated half-life of about 16 days). The Henry’s Law constant of VF (0.118 atmm3 mol1) indicates that VF is expected to volatilize rapidly from water surfaces. Due to its volatile property, VF is not persistent in nature and adsorption to sediment is not considered to be a natural process for VF in water. The half-life for volatilization from a model river (1-m deep) and a model pond (2-m deep) are 2 and 23.5 h, respectively. VF is not expected to bioconcentrate in aquatic organisms as it has a bioconcentration factor (BCF) of 4.7, whereas a BCF value greater than 1000 is required for its significant bioaccumulation. As VF remains as a gas under normal conditions, it readily evaporates to the atmosphere when released into soil. When dissolved in an aqueous solution, VF is very mobile in soil. Lack of sufficient data prevents to predict its biodegradation fate in soils.

운송 방법

UN1860 Vinyl fluoride, inhibited, Hazard Class: 2.1; Labels: 2.1-Flammable gas.

비 호환성

May polymerize. Inhibited with 0.2% terpenes to prevent polymerization. Violent reaction with oxidizers. May accumulate static electrical charges.

비닐 플루오르화물 준비 용품 및 원자재

원자재

준비 용품


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