Abstract:
PURPOSE: A refrigerant mixture containing difluoromethane, pentafluoroethane, 1,1,1-trifluoroethane is provided to substitute HCFC-22(chlorodifluoromethane, CHClF2) without worry of use restraint as being no risk of ozone layer destruction. CONSTITUTION: The refrigerant mixture comprises difluoromethane(CH2F2, HFC-32) as first component; pentafluoroethane(CHF2CF3, HFC-125) as second component; 1,1,1-trifluoro ethane(CH3CF3, HFC-143a) as third component; one component selected from cyclopropane(C3H6, RC-270), 1,1,1,2,3,3,3-heptafluoropropane(CF3CHFCF3, HFC-227ea), 1,1,1,2,2-pentafluoropropane(CH3CF2CF3, HFC-245cb), isobutane(CH(CH3)2CH3, R-600a), octafluorocyclobutane(C4F8, RC-318), 1,1,1,2,3,3-hexafluoropropane(CHF2CHFCF3, HFC- 236ea), butane(C4H10, R-600), bis(difluoromethyl)ether(CHF2OCHF2, HFE-134), penta fluoroethylmethylether(CF3CF2OCH3, HFE-245).
Abstract:
PURPOSE: Disclosed are a palladium catalyst supported on active carbon, a preparation method thereof and a hydrogenation reaction of chlorofluorocarbon to hydrofluorocarbon using the prepared catalyst. CONSTITUTION: The active carbon used as catalyst support is pretreated with a basic solution of 0.2-1M NaOH at 60-80deg.C for 1-5hours two or five times. And the acid treatment of a hydrochloric acid may be also conducted whenever after the base treatment or the hydrogen fluorine treatment or before loading of palladium species. The palladium species is impregnated by the adsorption precipitation method or the co-precipitation method. The hydrogenation reaction, dehalogenation, of chlorofluorocarbon to hydrofluorocarbon is selectively preformed to increase the yield of HFC-32.
Abstract:
The catalyst for fluorizing 1,1,1-trifluoro-2,2-dichloroethan consisted of a compound selected from a group comprising of magnesium and calcium, one or more metal element selected from a group comprising of zinc, cerium and nickel, and chrome and the preparing method thereof are disclosed. The mole ratio of chrome to magnesium or calcium is 1:1 to 1:32 and the mole ratio of chrome to metal element is at least 1:0.5. Thereby, the active ingredient of the catalyst is more uniformly distributed, thus the activity and the life of the catalyst are remarkably improved.
Abstract:
본원발명은 제1단계 반응에서 1,1,1-트리플루오로-2-클로로에탄과 불화수소와 염소를 반응시켜 HFC-134a와 HFC-125를 함께 제조하고, 제2단계 반응에서 제1단계 반응생성물에 트리클로로에틸렌을 첨가하여 HFC-133a를 제조한 다음, 제2단계 반응생성물에서 HFC-134a와 HFC-125 및 염화수소를 분리하고, 그 나머지 혼합물을 상기 제1단계 반응으로 순환시키는 것으로 이루어지는 HFC-134a와 HFC-125를 동시에 제조하는 방법에 관한 것이다.
Abstract:
The fine purification method for 1,1,1,2-tetrafluoroethane(HFC-134a) consists of the steps of; (a) separating the top flux of the distillation tower for HFC-134a; (b) neutralizing and drying; (c) removing hydrogen fluorine(HF); (d) removing water from the bottom flux of the distillation tower by drying. The HFC-134a contains no more than 100 ppm of HF and water respectively.
Abstract:
본 발명은 불화수소(HF)와 트리클로로에틸렌(TCE)을 출발 물질로 하여 중간체인 1-클로로-2,2,2-트리플루오로에탄(HCFC-133a)을 거쳐 1,1,1,2-테트라플루오로에탄(HFC-134a)을 제조하는 방법에 있어서, 반응 원료중 HF의 일부를 HCFC-133a 반응기로 유입전에 HFC-134a 제조 반응 생성물과 접촉시키고, 나머지 HF 및 TCE 원료를 HCFC-133a 제조 반응기에 2개소 이상의 구간으로 분할하여 공급함으로써 반응을 효율적으로 수행하는 방법이 제공된다. 즉, HCFC-133a 제조 반응 전반에 걸쳐 반응기 내부 온도의 변화폭을 좁게 유지시킴으로써 촉매 활성의 제한, 다량의 부산물 생성 및 낮은 수율 등의 문제점이 크게 개선된다.