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    • 5. 发明授权
    • Method for co-production of 1,1-difluoroethane and vinyl chloride
    • US11970430B2
    • 2024-04-30
    • US17627122
    • 2021-06-25
    • Zhejiang Quhua Fluor-Chemistry Co Ltd
    • Huimei YuJiangyong HongBo YangYang ZhaoYan ZhangLinhui LiYawen Ren
    • C07C17/20B01J23/26C07C17/383
    • C07C17/20B01J23/26C07C17/383
    • The present invention provides a method for the co-production of 1,1-difluoroethane and vinyl chloride, including: (a) vaporizing dichloroethane and hydrogen fluoride, and delivering the vaporized dichloroethane and hydrogen fluoride into a reactor for a catalytic reaction under the action of a catalyst to obtain a reaction product; (b) delivering the reaction product into a first rectifying tower for separation to obtain an overhead product from the first rectifying tower and a bottom product from the first rectifying tower; (c) delivering the overhead product from the first rectifying tower into a second rectifying tower for separation to obtain hydrogen chloride and a bottom product from the second rectifying tower; (d) delivering the bottom product from the second rectifying tower into a purifying tower for purification to obtain an overhead product from the purifying tower; (e) simultaneously delivering the overhead product from the purifying tower and a saturated organic solvent into a third rectifying tower for separation to obtain a 1,1-difluoroethane product and a bottom product from the third rectifying tower; and (f) delivering the bottom product from the third rectifying tower into a fourth rectifying tower for separation to obtain a vinyl chloride product and a bottom stream from the fourth rectifying tower. The present invention has the advantages of simple process, high conversion rate, and good product quality.
    • 7. 发明授权
    • Method for preparing 2,3,3,3-tetrafluoropropene
    • 制备2,3,3,3-四氟丙烯的方法
    • US09346724B2
    • 2016-05-24
    • US14967242
    • 2015-12-11
    • Zhejiang Quhua Fluor-Chemistry Co., Ltd.
    • Jun LeiBo YangYan ZhangYang ZhaoHuadong ZhouQiang ZhouGang Su
    • C07C17/20C07C17/00C07C17/383C07C21/18C07C17/087
    • C07C17/20C07C17/087C07C17/204C07C17/206C07C17/383C07C21/18
    • A method for preparing 2,3,3,3-tetrafluoropropene, including: a) heating and vaporizing hydrogen fluoride and 1,1,2,3-tetrachloropropene (TCP), and introducing hydrogen fluoride and TCP to a first reactor for reaction in the presence of an A-type catalyst to yield a first product mixture including 2,3-dichloro-3,3-difluoropropene (“HCFO-1232xf”), where the mole ratio between hydrogen fluoride and TCP is between 5:1 and 60:1, the reaction temperature is between 200 and 500° C., and the space velocity is between 200 and 2000 h−1; b) preheating the first product mixture including HCFO-1232xf, introducing the first product mixture including HCFO-1232xf to a second reactor for reaction in the presence of a B-type catalyst to yield a second product mixture including HFO-1234yf, where the temperature of the preheated first product mixture including HCFO-1232xf is higher than the reaction temperature of the first reactor and lower than the reaction temperature of the second reactor.
    • 一种制备2,3,3,3-四氟丙烯的方法,包括:a)加热和蒸发氟化氢和1,1,2,3-四氯丙烯(TCP),并将氟化氢和TCP引入第一反应器进行反应 存在A型催化剂以产生包含2,3-二氯-3,3-二氟丙烯(“HCFO-1232xf”)的第一产物混合物,其中氟化氢和TCP之间的摩尔比为5:1至60:1 :1,反应温度在200〜500℃之间,空速在200〜2000h -1之间; b)预热包括HCFO-1232xf在内的第一产物混合物,将包含HCFO-1232xf的第一产物混合物引入第二反应器,以在B型催化剂存在下进行反应,得到包含HFO-1234yf的第二产物混合物,其中温度 包括HCFO-1232xf的预热的第一产物混合物的温度高于第一反应器的反应温度并低于第二反应器的反应温度。