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    Condensates
    3.
    发明申请
    Condensates 失效
    冷凝水

    公开(公告)号：US20020107153A1

    公开(公告)日：2002-08-08

    申请号：US10109848

    申请日：2002-04-01

    申请人： BP OIL INTERNATIONAL LIMITED

    发明人： Spencer Edwin Taylor ,  Michael John Wilson

    IPC分类号： C10M129/14 ,  C10L001/18 ,  C07C069/94

    CPC分类号： C10M159/22 ,  B01D17/045 ,  B01D17/047 ,  C07C65/17 ,  C07C69/94 ,  C10L1/1981 ,  C10L10/04 ,  C10M145/20 ,  C10M2209/00 ,  C10M2209/02 ,  C10M2209/10 ,  C10M2209/101 ,  C10N2240/10 ,  C10N2240/101 ,  C10N2240/104 ,  C10N2240/106

    摘要： A cyclic compound comprising m units of the formula Ia. 1 and n units of the formula (Ib) 2 joined together to form a ring, wherein Y and Y2 are divalent bridging groups which may be the same or different in each unit; R0 is H or (C1-C6) alkyl or is a metal or ammonium cation; R5 is H or (C1-C60) alkyl or OH group; j is 1 or 2; R3 is hydrogen, a hydrocarbyl or a hetero-substituted hydrocarbyl group; each of R1, R2 and R4, which may be the same or different, is hydroxyl, hydrogen, hydrocarbyl or hetero-substituted hydrocarbyl, with the provisos that i) at least one of R1, R2, R4 is hydroxyl, and mnulln is 4 to 20, m is 1-8 and n is at least 3, and ii) in formula Ia at least one OH group is in the meta or para position to the COOR0 group and/or at least one R5 group is OH.

    摘要翻译： 包含m个式Ia化合物的环状化合物。 和式（Ib）的n个单元连接在一起形成环，其中Y和Y2是每个单元可以相同或不同的二价桥连基团; R 0是H或（C 1 -C 6）烷基或是金属或铵阳离子; R5是H或（C1-C60）烷基或OH基; j为1或2; R3是氢，烃基或杂取代的烃基; R 1，R 2和R 4各自可以相同或不同，是羟基，氢，烃基或杂取代的烃基，条件是i）R 1，R 2，R 4中的至少一个是羟基，m + n 为4至20，m为1-8且n为至少3，和ii）在式Ia中，至少一个OH基位于COOR0基团的间位或对位，和/或至少一个R 5基团为OH。

    Polycyclic polyphenols
    9.
    发明授权
    Polycyclic polyphenols 失效
    多环多酚

    公开(公告)号：US3047503A

    公开(公告)日：1962-07-31

    申请号：US4173560

    申请日：1960-07-11

    申请人： SHELL OIL CO

    发明人： JAFFE GUNTER S ,  ROCKLIN ALBERT L ,  WINKLE JOHN L VAN

    IPC分类号： C07C37/16 ,  C07C39/15 ,  C07F9/16 ,  C08F2/38 ,  C08K5/13 ,  C08K5/372 ,  C08K5/40 ,  C09K15/08 ,  C10L1/183 ,  C10M129/14

    CPC分类号： C10M129/14 ,  C07C37/16 ,  C07C39/15 ,  C07C2603/24 ,  C07F9/16 ,  C08F2/38 ,  C08K5/13 ,  C08K5/372 ,  C08K5/40 ,  C09K15/08 ,  C10L1/1835 ,  C10M2207/023 ,  C10M2207/024 ,  C10M2219/066 ,  C10M2219/068 ,  C10M2219/082 ,  C10M2219/085 ,  C10M2221/043 ,  C10M2223/04 ,  C10M2223/042 ,  C10M2223/047 ,  C10M2290/02 ,  C10N2210/02 ,  C10N2250/10 ,  Y10S8/09 ,  Y10S524/925

    摘要： As anti-oxidants for gasoline, kerosene, furnace oils, mineral lubricating oils and greases, use is made of polynuclear phenols in which an aromatic hydrocarbon group having condensed benzene nuclei is linked to one or more 3, 5-dialkyl-4-hydroxybenzyl substituents attached directly to the ring system. The specified products include 9, 10-bis (3, 5-di-tert.-butyl-4-hydroxybenzyl) anthracene, 1, 4-bis(3, 5-diisopropyl-4-hydroxybenzyl) naphthalene, alpha-3, 5-diisopropyl-4-hydroxybenzyl-naphthalene, 1-methyl-3 (3-methyl-5-tert.-butyl-4-hydroxybenzyl)naphthalene, 1,4,5,8- tetra(3,5-di-tert. butyl-4-hydroxybenzyl) naphthalene, 9,10-bis(3-methyl-5-tert.-hexyl-4-hydroxybenzyl) phenanthrene, 1,4,5,8,9,10-hexa (3,5-diisopropyl-4-hydroxybenzyl) anthracene, and 5, 6, 11, 12-tetra (3,5-di-tert.-butyl-4-hydroxybenzyl) naphthacene. Products derived from chrysene, pyrene, benzanthracene, pentacene, dibenzanthracene and coronene are also specified. A synergistic effort is produced if the antioxidants described above are used in association with sulphur compounds of the following types. (1) Compounds of the type R1-Sx-R2, where X is a whole number and R1 and R2 are similar or dissimilar organic groups bound to Sx by means of carbon atoms, e.g. compounds of the foumula where R and R1 are similar or dissimilar hydrocarbon groups of 6-20 carbon atoms and n is 1-6, e.g. dilaurylthio-dipropionate, or sulphides of the types R1-CH2-CH2-Sx-R2 or R1-CH2-CH2- Sx-CH2-CH2 -R2, where X is a whole number and R1 and R2 are similar or dissimilar aliphatic or aromatic groups. (2) Compounds of the general formula where M is a metal of Group II of the Periodic System and R1 and R2 are hydrocarbon groups of 1-6 carbon atoms. (3) Trialkyl trithiophosphites having 6-20 carbon atoms in the alkyl groups. (4) Polymeric products su:h as polyalkoxyalkyl sulphides (-R1-O-R1-S-)x,polyalkoxy=alkoxyalkyl sulphides (-R1-O-R2-O-R1-S-)x and polyhydroxyalkyl sulphides (-R1 (OH)-S-)x, such products being obtainable by reacting an unsaturated ether, e.g. diallyl ether, with hydrogen sulphide.ALSO:As anti-oxidants for polyolefines, synthetic rubbers and liquid ethylenically unsaturated monomers, use is made of polynuclear phenols in which an aromatic hydrocarbon group having condensed benzene nuclei is linked to a 3,5-dialkyl-4-hydroxybenzyl substituent attached directly to the ring system. The aromatic hydrocarbon group preferably contains 2-6 benzene nuclei and may be substituted with alkyl groups preferably having not more than 4 carbon atoms. The alkyl groups in the 3,5-dialkyl-4-hydroxybenzyl residue preferably contain not more than 8 carbon atoms. The specified products includes 9,10-bis(3,5-di-tert.-butyl-4-hydroxybenzyl) anthracene, 1,4-bis(3,5-diisopropyl-4-hydroxybenzyl) naphthalene, alpha - 3,5 - diisopropyl - 4 - hydroxybenzyl - naphthalene, 1-methyl-3(3-methyl-5-tert.-butyl-4-hydroxybenzyl) naphthalene, 1,4,5,8-tetra(3,5-ditert.-butyl-4-hydroxybenzyl) naphthalene, 9,10-bis(3-methyl-5-tert.-hexyl-4-hydroxybenzyl) phenanthrene, 1,4,5,8,9,10-hexa(3,5-diisopropyl-4-hydroxybenzyl) anthracene, and 5,6,11,12-tetra-(3,5-di-tert.-butyl-4-hydroxybenzyl) naphthacene. Products derived from chrysene, pyrene, benzanthracene, pentacene, dibenzanthracene and coronene are also specified. A number of materials to which the phenols may be applied are specified. The proportion of antioxidant may be 0,0001-10% by weight. A synergistic effect is produced if the antioxidants described above are used in association with sulphur compounds of the following types. (1) Compounds of the type R1-Sx-R2, where X is a whole number and R1 and R2 are similar or dissimilar organic groups bound to Sx by means of carbon atoms, e.g. compounds of the formula where R and R1 are similar or dissimilar hydro-carbon groups of 6-20 carbon atoms and n is 1-6, e.g. dilaurylthiodipropionate, or sulphides of the types R1-CH2-CH2-Sx-R2 or R1-CH2-CH2-Sx-CH2-CH2 -R2, where X is a whole number and R1 and R2 are similar or dissimilar aliphatic or aromatic groups. (2) Compounds of the general formula where M is a metal of Group II of the periodic system and R1 and R2 are hydrocarbon groups of 1-6 carbon atoms. (3) Trialkyl trithiophosphites having 6-20 carbon atoms in the alkyl groups. (4) Polymeric products such as polyalkoxyalkyl sulphides (-R1-O-R1-S-)x, polyalkoxyalkoxyalkyl sulphides (-R1-O-R2-O-R1-S-)x and polyhydroxyalkyl sulphides (-R1(OH)-S-)x, such products being obtainable by reacting an unsaturated ether, e.g. diallyl ether, with hydrogen sulphide. Rubber and plastic compositions treated according to the invention may contain pigments, fillers, antiozonants and curing agents.ALSO:The invention comprises polynuclear phenols in which an aromatic hydrocarbon group having condensed benzene nuclei is linked to a 3,5-dialkyl-4-hydroxybenzyl substituent attached directly to the ring system. The aromatic hydrocarbon group preferably contains 2-6 benzene nuclei and may be substituted with alkyl groups preferably having not more than 4 carbon atmos. The alkyl groups in the 3,5-dialkyl-4-hydroxybenzyl residue preferably contain not more than 8 carbon atoms. The products may be prepared by condensing an aromatic hydrocarbon having condensed benzene nuclei with a 3,5-dialkyl-4-hydroxybenzyl alcohol in the presence of a Friedel-Crafts catalyst or sulphuric acid, preferably in the presence of a dehydrating agent, e.g. phosphorus pentoxide, and optionally in the presence of an inert solvent, a number of which are specified. The reaction may be effected at -15-100 DEG C., preferably at atmospheric pressure. The specified Friedel-Crafts catalysts include zirconium tetrachloride, tantalum pentachloride, beryllium chloride, titanium tetrachloride and tin tetrachloride. The specified products include 9,10-bis(3,5-di-tert.-butyl-4-hydroxybenzyl)anthracene, 1,4-bis(3,5- diisoprophyl-4- hydroxybenzyl-naphthalene, alpha-3,5-diisopropyl- 4-hydroxybenzyl-naphthalene, 1-methyl- 3(3-methyl- 5-tert.-butyl- 4-hydroxybenzyl)-naphthalene, 1,4,58- tetra(3,5-di-tert.-butyl- 4-hydroxybenzyl)naphthalene, 9,10-bis(3-methyl- 5-tert.-hexyl- 4-hydroxybenzyl) phenanthrene, 1,4,5,8,9,10- hexa(3,5-diisopropyl-4-hydroxybenzyl)anthracene, and 5,6,11, 12-tetra(3,5- di-tert.- butyl-4- hydroxybenzyl) naphthacene. Products derived from chrysene, pyrene, benzanthracene, pentacene, dibenzanthracene and coronene are also specified. The products are useful as antioxidants and for protecting materials against thermal and ultra-violet degradation. Materials to which the products may be applied include polyolefines, synthetic rubbers and liquid ethylenically unsaturated monomers, a number of each of which are specified, and also natural rubber, gasoline, kerosine, furnace oils, lubricating oils and greases. A synergistic effect is produced if the antioxidants described above are used in association with certain sulphur compounds (see Groups III and IV(a)).