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    • 2. 发明授权
    • Preparation of vat dyes and pigments of the perinone series
    • PERINONE系列增值税和色素的制备
    • US5074919A
    • 1991-12-24
    • US427456
    • 1989-10-26
    • Erwin DietzGustav KapaunSiegfried Schiessler
    • Erwin DietzGustav KapaunSiegfried Schiessler
    • C09B57/12
    • C09B57/12
    • The conventional condensation of naphthalene-1,4,5,8-tetracarboxylic acid with 1,2-diaminobenzene gives the resulting naphthoylenebisbenzimidazole isomers together in the cis and trans form. It is desirable to shift the isomer ratio of the mixture obtained toward the desirable trans product and to reduce the amount of cis product obtained. It is also desirable to develop a process of preparation which optimizes the yield and improves the waste water situation.This object is achieved according to the invention by subjecting virtually stoichiometric amounts of the starting compounds to a precondensation at 60.degree. to 110.degree. C. in an aqueous medium and then completing the condensation in the aqueous medium in a second stage at 130.degree. to 180.degree. C.
    • 萘-1,4,5,8-四羧酸与1,2-二氨基苯的常规缩合使得所得的萘并苯并二苯并咪唑异构体以顺式和反式形式一起。 期望将获得的混合物的异构体比例转化为所需的反式产物,并减少所获得的顺式产物的量。 还需要开发一种优化产量并改善废水情况的制备方法。 根据本发明,该目的是通过在水性介质中对实际上化学计量的起始化合物进行60℃至110℃的预缩合,然后在130℃至180℃的第二阶段中在水性介质中完成冷凝 DEG C.
    • 5. 发明授权
    • Process for the preparation of pigment preparations of the anthanthrone
series
    • 制备ANTHANTHRONE系列染料制剂的方法
    • US5071483A
    • 1991-12-10
    • US409522
    • 1989-09-19
    • Erwin DietzManfred UrbanSiegfried Schiessler
    • Erwin DietzManfred UrbanSiegfried Schiessler
    • C09B3/60B01F17/16B01F17/32C09B57/00C09B57/04C09B57/08C09B57/12C09B67/20C09B67/22
    • C09B67/0033
    • A process for the preparation of pigment preparations of the anthanthrone series, which comprises subjecting anthanthrone crude pigments to aqueous pearl milling in the presence of dispersants of the formulaeQ.sub.1 -[A.sub.1 -X].sub.n (I)and/or[Q.sub.2 -A.sub.2 ].sub.z -Y (II)in which in formula (I) Q.sub.1 is the radical of an anthanthrone, azo, isoindolinone, diketopyrrolopyrrole or perinone compound, A.sub.1 is a direct bond or --O--, --S--, --NR.sub.3, --CO--, --SO.sub.2 --, --CR.sub.4 R.sub.5 -- or arylene, X is a group ##STR1## or a heterocyclic radical having at least one nitrogen atom, and R.sub.3, R.sub.4, R.sub.5, R.sub.6 and R.sub.7 are hydrogen atoms or saturated or unsaturated alkyl groups and n is 1 to 4, and in formula (II) Q.sub.2 is a radical of the formula ##STR2## in which R.sub.1 is hydrogen, halogen, alkyl, alkoxy or cyano, or, in the case that m.sub.1 >1, R.sub.1 can also be a combination of these substituents, R.sub.2 is hydrogen, halogen, an alkyl, alkoxy or cyano or, in the case that m.sub.2 >1, R.sub.2 can also be a combination of these substituents, m.sub.1 and m.sub.2 are 1 to 4, A.sub.2 is --(CH.sub.2).sub.p --, CR.sub.8 R.sub.9 --, arylene, --O--, --NR.sub.10 --, --CO-- or --SO.sub.2 --, in which p is from 1 to 6, R.sub.8, R.sub.9 and R.sub.10 are hydrogen or alkyl, Y is dimethylamino or diethylamino or an imidazole or piperazine radical and z is 1 or 2, and subjecting the suspensions of the prepigment preparations obtained to a heat treatment at temperatures from 20.degree. to 200.degree. C.
    • 一种制备蒽烷系列颜料制剂的方法,该方法包括在式Q1- [A1-X] n(I)和/或[Q2-A2]的分散剂存在下使蒽醌粗颜料进行水珍珠研磨, 其中式(I)中的QY(II)Q1为蒽醌,偶氮,异吲哚啉酮,二酮吡咯并吡咯或百草酮化合物的基团,A1为直接键或-O - , - S - , - NR 3,-CO-, - SO 2 - ,-CR 4 R 5 - 或亚芳基,X是具有至少一个氮原子的基团,或者R 3,R 4,R 5,R 6和R 7是氢原子或饱和或不饱和烷基,n是1 至(4)中,并且在式(II)中,Q2是下式的基团,其中R 1是氢,卤素,烷基,烷氧基或氰基,或者在m1> 1的情况下,R 1也可以是 这些取代基R2是氢,卤素,烷基,烷氧基或氰基,或者在m2≥1的情况下,R2也可以是这些取代基的组合,m1和m2是1-4,A2是 - (CH2)p - ,CR8R9-, 亚芳基,-O-,-NR 10 - , - CO-或-SO 2 - ,其中p为1至6,R 8,R 9和R 10为氢或烷基,Y为二甲基氨基或二乙基氨基或咪唑或哌嗪基,z为 为1或2,对得到的预标准剂的悬浮液进行20〜200℃的热处理。
    • 6. 发明授权
    • Pigment preparations
    • 颜料制剂
    • US5071482A
    • 1991-12-10
    • US410159
    • 1989-09-20
    • Erwin DietzSiegfried SchiesslerManfred Urban
    • Erwin DietzSiegfried SchiesslerManfred Urban
    • C09B67/20C08K5/3442C08K5/3447C08K9/04C09B57/12C09B67/22C09D7/12C09D11/02D01F1/04
    • C09B67/0033C09B57/12
    • Pigment preparations consisting of organic pigments and basic additives of the general formula I(Q-A).sub.x Y (I)in which Q is a radical of the formula II ##STR1## in which R.sup.1 is halogen, an alkyl, alkoxy or cyano group, R.sup.2 is halogen, m and n are integers from 0 to 4, A is a chemical bond or a divalent group from the series consisting of --(CH.sub.2).sub.p --, --CR.sup.3 R.sup.4 --, arylene, --S--, --O-- and --NR.sup.5 --, in which p is an integer from 1 to 12, R.sup.3 is hydrogen or alkyl, R.sup.4 is alkyl and R.sup.5 is hydrogen or alkyl, Y is a tertiary nitrogen atom or a group ##STR2## in which R.sup.6, R.sup.7 and R.sup.8 are alkyl or alkenyl or a cycloaliphatic or araliphatic radical or an alkyleneheteroaryl radical, or Y is a saturated or unsaturated heterocyclic radical in which at least one tertiary nitrogen atom is included in the meanings mentioned for Y and x is a number from 1 to 6.
    • 由有机颜料和通式I(QA)x Y(I)的碱性添加剂组成的颜料制剂,其中Q是式II的基团,其中R 1是卤素,烷基,烷氧基或氰基 ,R2是卤素,m和n是0-4的整数,A是由 - (CH2)p-,-CR3R4 + 13,亚芳基,-S-,-O- 和-NR5-,其中p是1至12的整数,R3是氢或烷基,R4是烷基,R5是氢或烷基,Y是叔氮原子或基团,其中R6,R7和 R8是烷基或烯基或脂环族或芳脂族基或亚烷基杂芳基,或Y是饱和或不饱和的杂环基,其中在Y中提及的含义中至少含有一个叔氮原子,x是1至6的数 。
    • 8. 发明授权
    • Process for preparing 1,3,6,8-tetrabromopyrene
    • 制备1,3,6,8-四溴芘的方法
    • US4684753A
    • 1987-08-04
    • US907400
    • 1986-09-12
    • Siegfried SchiesslerErnst Spietschka
    • Siegfried SchiesslerErnst Spietschka
    • C07C17/10C07C17/00C07C17/12C07C25/22C07C67/00C07C17/02
    • C07C17/12
    • Process for preparing 1,3,6,8-tetrabromopyrene by brominating pyrene in aqueous suspension with simultaneous reoxidation of the resulting hydrogen bromide to bromine by means of an oxidizing agent, which comprises reacting pyrene in a highly concentrated aqueous suspension having a pyrene-water weight ratio of 1:1.2 to 2 with bromine at temperatures of 40.degree. to 65.degree. C. with simultaneous reoxidation of the resulting hydrogen bromide to bromine using an oxidizing agent, completing the bromination by heating the reaction mixture to temperatures of 70.degree. to 130.degree. C., reducing excess bromine with a reducing agent to hydrogen bromide and subjecting the 1,3,6,8-tetrabromopyrene formed, preferably without intermediate isolation, to an alkaline aftertreatment at temperatures of 40.degree. to 100.degree. C. within the pH range 8.5 to 12.
    • 通过在水悬浮液中溴化芘制备1,3,6,8-四溴芘的方法,同时通过氧化剂将所得溴化氢再次氧化成溴,该方法包括使芘在具有芘水的高度浓缩的水悬浮液中 重量比为1:1.2至2,溴在40至65℃的温度下,同时使用氧化剂将所得溴化氢再次氧化成溴,通过将反应混合物加热至70°至130° 用还原剂将过量的溴还原成溴化氢,并将形成的1,3,6,8-四溴芘(优选不经中间分离)在40℃至100℃的温度下进行碱性后处理 范围8.5到12。