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high haertbare to elastomers on the basis of polysiloxan polyurethane mischpoly - european union

机译:基于聚硅氧烷-聚氨酯杂化的高弹性体对弹性体的保护-欧洲联盟

摘要

1532971 Silicone moulding compositions containing silylated polyurethane prepolymers BAYER AG 19 Sept 1975 [21 Sept 1974] 38530/75 Heading C3T A moulding composition comprises (a) a polysiloxane HO(R 2 SiO) n H, wherein each R is H, alkyl, alkaryl, aryl or haloalkyd and n is at least 3; (b) a silylated polyurethane prepolymer wherein RSP1/SP is a C 1-8 alkyl or C 8-14 cycloalkyl radical, RSP11/SP is an optionally halo- or cyanosubstituted C 1-10 alkyl, C 4-10 cycloalkyl or C 6-10 aryl radical; RSP111/SP is H, CH 3 - or C 6 S-; RSP1111/SP is H or as RSP11/SP; QSP1/SP is a C 4-36 alkylene, C 4-14 cycloalkylene, C 7-46 aralkylene or alkarylene or a C 6-14 arylene radical; X is -O-, -NH- or -NY- (Y being C 1-8 alkyl); and Q is derivable from a compound Q(XH) 2 of M.W. 200-80,000, containing at least one ester, ether, urethane, urea, carbonate or amide group and optionally at least one siloxane group; and (c) a compound containing at least 3 hydrolysable groups attached to each Si atom. In Example 1 component (b) is prepared by treating (i) a polypropylene glycol with (ii) TDI and (iii) C 6 H 11 -NH-CH 2 SiMe 2 OEt in 1 : 2 : 2 molar ratio. In Examples 5-9 and 12 there is used instead of (i) an adipic acid-hexamethylene glycolneopentyl glycol (Ex. 5), instead of (ii) hexamethylene or isophorone diisocyanate (Examples 7 and 8), instead of (iii) C 6 H 5 -CH 2 -NH-CH 2 SiMe 2 OEt or (Ex. 12), and molar ratios of about 2 : 3 : 1 (Examples 6-8) or 5 : 6 : 1 (Ex. 9); additional polysiloxane diol is then added in Examples 5-8. In Examples 4-12 moulding compositions are made from 30 p.b.w. of (a) a polydimethylsiloxane diol of 45,000 c.p., 31 p.b.w. of (b), 5 p.b.w. of (c) MeSi(ON=CMeEt) 3 , 24 p.b.w. of (d) a trimethylsilyl-terminated polydimethylsiloxane, and 10 p.b.w. SiO 2 and 0À05 p.b.w. of dibutyltin dilaurate; in Examples 1-3 20, 28 and 20 p.b.w. of (a) are used with 63, 55 and 41 p.b.w. (b), 7, 7 and 5 p.b.w. of (c) and 0, 0 and 24 p.b.w. (d), 10 p.b.w. silica and 0À05 of catalyst.
机译:1532971包含甲硅烷基化聚氨酯预聚物的硅树脂模塑组合物,BAYER AG 1975年9月19日[1974年9月21日]标题C3T。模塑组合物包含(a)聚硅氧烷HO(R 2 SiO)n H,其中每个R为H,烷基,烷芳基,芳基或卤代烷基且n为至少3; (b)甲硅烷基化的聚氨酯预聚物,其中R 1 是C 1-8烷基或C 8-14环烷基,R 11 是任选被卤素或氰基取代的C 1 -10个烷基,C 4-10环烷基或C 6-10芳基; R 111 为H,CH 3-或C 6 S-; R 1111 是H或R 11 ; Q 1 是C 4-36亚烷基,C 4-14环亚烷基,C 7-46亚芳基或亚芳基或C 6-14亚芳基。 X为-O-,-NH-或-NY-(Y为C 1-8烷基); Q衍生自M.W. 200-80,000的化合物Q(XH)2,其含有至少一个酯,醚,氨基甲酸酯,脲,碳酸酯或酰胺基团和任选地至少一个硅氧烷基团; (c)含有与每个Si原子连接的至少3个可水解基团的化合物。在实施例1中,组分(b)通过用(ii)TDI和(iii)C 6 H 11 -NH-CH 2 SiMe 2 OEt以1:2:2的摩尔比处理聚丙二醇来制备。在实施例5-9和12中,代替(i)使用己二酸-六亚甲基二醇新戊二醇(实施例5),代替(ii)使用六亚甲基或异佛尔酮二异氰酸酯(实施例7和8)代替(iii)C 6 H 5 -CH 2 -NH-CH 2 SiMe 2 OEt或(实施例12),且摩尔比为约2:3:1(实施例6-8)或5:6:1(实施例9);然后在实施例5-8中加入另外的聚硅氧烷二醇。在实施例4-12中,模塑组合物由30p.b.w.制成。 (a)45,000 c.p.,31 p.b.w.的聚二甲基硅氧烷二醇(b),下午5点(c)MeSi(ON = CMeEt)3,p.b.w。24 (d)三甲基甲硅烷基封端的聚二甲基硅氧烷,和10 p.b.w. SiO 2和0‑05 p.b.w.二月桂酸二丁基锡;在实施例1-3中,p.b.w为20、28和20。 (a)中的分别与63、55和41 p.b.w. (b),7、7和5 p.b.w. (c)和0、0和24 p.b.w. (d),晚上10点二氧化硅和0‑05的催化剂。

著录项

  • 公开/公告号ATA720075A

    专利类型

  • 公开/公告日1979-05-15

    原文格式PDF

  • 申请/专利权人 BAYER AKTIENGESELLSCHAFT;

    申请/专利号AT19750007200

  • 发明设计人

    申请日1975-09-19

  • 分类号C08L83/04;

  • 国家 AT

  • 入库时间 2022-08-22 20:19:33

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