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    • 2. 发明授权
    • Weather-resistant resin composition for powder coating
    • 耐候性粉末涂料用树脂组合物
    • US6084035A
    • 2000-07-04
    • US180199
    • 1998-11-04
    • Satoru MiyakeHisao IkedaToshinari KodaMotohiko Hidaka
    • Satoru MiyakeHisao IkedaToshinari KodaMotohiko Hidaka
    • C08G59/18C08G59/24C09D163/00C08F20/00C08K5/49
    • C08G59/245C08G59/18C09D163/00Y10S524/904
    • A resin composition for powder coating, comprising(A) a carboxyl group-containing resin having a number average molecular weight of 1000 to 20000, an acid value of 5 to 200 and a glass transition temperature of 30 to 120.degree. C.,(B) bis(.beta.-methylglycidyl)terephthalate of the formula (1): ##STR1## as a curing agent, and (D) at least one compound selected from the group consisting of amines having the linkage of the formula (2): ##STR2## in the molecule, a triarylphosphines and onium salts as a ring-opening polymerization inhibitor, the equivalent ratio of (.beta.-methylglycidyl group of the component (B))/(carboxyl group of the component (A)) being 0.5 to 3.0. The composition can give a product of curing excellent in impact resistance, weathering resistance and so on.
    • PCT No.PCT / JP97 / 01666 Sec。 371日期:1998年11月4日 102(e)1998年11月4日日期PCT提交1997年5月19日PCT公布。 WO97 / 44400 PCT出版物 日期1997年11月27日一种粉末涂料用树脂组合物,其含有(A)数均分子量为1000〜20000,酸值为5〜200,玻璃化转变温度为30〜120℃的含羧基的树脂 C,(B)式(1)的双(β-甲基缩水甘油基)对苯二甲酸酯:作为固化剂,和(D)至少一种选自具有式(2)键的胺的化合物: 在分子中,作为开环聚合抑制剂的三芳基膦和鎓盐,成分(B)的(β-甲基缩水甘油基)/(成分(A)的羧基)的当量比为0.5〜3.0。 该组合物可以得到耐冲击性,耐候性等优异的固化性产品。
    • 9. 发明授权
    • Method for producing purified epoxy compound
    • 纯化环氧化合物的制备方法
    • US5892065A
    • 1999-04-06
    • US892198
    • 1997-07-14
    • Suketoshi TsukamotoTakami OnoHisao IkedaMotohiko Hidaka
    • Suketoshi TsukamotoTakami OnoHisao IkedaMotohiko Hidaka
    • C07D301/27C07D301/32C07D303/16C07D301/02C07D405/12
    • C07D303/16C07D301/32C08G59/025
    • A 2,3-epoxypropyl derivative or a 2-methyl-2,3-epoxypropyl derivative of a compound having carboxyl groups or amido groups is produced as a purified product having an epoxide equivalent of 1.0 to 1.1 times the theoretical epoxide equivalent of the derivative, an ionic halogen content of 10 ppm or less, transparency when molten and a stability against increase in the epoxide equivalent when stored at 150.degree. C. for 24 hours, by a process comprising steps (A) reacting 1.2 to 60 mol of an epihalohydrin or a 2-methyl-epihalohydrin with 1 mol of active hydrogen atoms of the carboxyl or amido group of the compound in the presence of a particular catalyst, thereby forming a reaction product containing a 2-hydroxy-3-halopropyl derivative or a 2-hydroxy-2-methyl-3-halopropyl derivative, (B) dehydrohalogenating the derivative by adding to the reaction product a sufficient amount of an alkali metal hydroxide thereby forming a final slurry containing the 2,3-epoxypropyl derivative of the 2-methyl-2,3-epoxypropyl derivative and the alkali metal halide, (C) washing the final slurry or a liquid product formed by removing the alkali metal halide from the final slurry thereby forming a refined liquid containing the derivative, and (D) removing by evaporation the epihalohydrin or the 2-methyl-epihalohidrin from the refined liquid, thereby forming the 2,3-epoxypropyl derivative or the 2-methyl-2,3-epoxypropyl derivative as the purified product.
    • 制备具有羧基或酰胺基的化合物的2,3-环氧丙基衍生物或2-甲基-2,3-环氧丙基衍生物作为纯化产物,其环氧当量为衍生物的理论环氧当量的1.0-1.1倍 ,离子卤素含量为10ppm以下,当熔融时的透明度和在150℃下储存24小时时的环氧当量增加的稳定性,通过包括以下步骤的方法:(A)使1.2至60摩尔的表卤代醇 或具有1摩尔化合物的羧基或酰胺基的活性氢原子的2-甲基 - 表卤代醇在特定催化剂的存在下反应,从而形成含有2-羟基-3-卤代丙基衍生物或2-羟基-3-卤代丙基衍生物的反应产物, 羟基-2-甲基-3-卤代丙基衍生物,(B)通过向反应产物中加入足够量的碱金属氢氧化物脱卤化氢,从而形成含有2-甲基-3-氯丙基衍生物的2,3-环氧丙基衍生物的最终浆液, 2,3-环氧丙基衍生物和碱金属卤化物,(C)洗涤最终浆料或通过从最终浆料中除去碱金属卤化物形成的液体产物,从而形成含有该衍生物的精制液体,(D)通过蒸发除去 来自精制液体的表卤代醇或2-甲基 - 表卤代醇,由此形成2,3-环氧丙基衍生物或2-甲基-2,3-环氧丙基衍生物作为纯化产物。