序号 | 专利名 | 申请号 | 申请日 | 公开(公告)号 | 公开(公告)日 | 发明人 |
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181 | Coal tar and mercaptan-terminated polymer compositions | US3635864D | 1969-10-28 | US3635864A | 1972-01-18 | MCCARTHY WILLIAM J; IRELAND ROBERT W |
BLENDS OF MERCAPTAN-TERMINATED LIQUID COPOLYMERS AND COAL TAR FORM CURABLE SEALANT COMPOSITIONS THAT MAY BE CURED WITH SUITABLE CURING AGENTS TO FORM ELASTOMERS HAVING ADHESION TO CEMENTITIOUS MATERIALS AND ARE SUITABLE FOR SEALING CONCERTE AND FORMING ELASTOMERIC GASKETS.
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182 | Tricyclic polysulfur compounds and process for their preparation | US3621032D | 1969-03-06 | US3621032A | 1971-11-16 | ARIYAN ZAVEN S; MARTIN ROBERT L |
Novel polysulfur tricyclic compounds wherein two substituted aromatic rings are attached to each other through two tetrasulfide links.
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183 | Method of treating liquid dithiols and liquid dithiols-rubber blends with alkanolamines and methyl amino-alkyl phenols and compositions thereof | US3520854D | 1966-09-12 | US3520854A | 1970-07-21 | WARNER PAUL F |
184 | Reaction products of multiaziridino compounds and hydrogen sulfide adhesive compositions | US3514369D | 1967-05-10 | US3514369A | 1970-05-26 | UELZMANN HEINZ; HIDINGER DAVID C JR |
185 | Adhesive plasticised sulphur containing an olefine polymer | US3465064D | 1967-03-02 | US3465064A | 1969-09-02 | SIGNOURET JEAN-BAPTISTE |
1,182,171. Treating polymers; polysulphide products; sulphur compositions. SOC. NATIONALE DES PETROLES D'AQUITAINE. 7 March, 1967 [11 March, 1966], No. 10685/67. Headings C3N, C3P and C3R. [Also in Divisions C5 and El] ' Plastic reaction products are prepared by heating while stirring at 100‹ to 200‹ C. 40 to 95 parts by weight of molten sulphur, 0-05 to 59.5 parts by weight of a dithiolpolysulphide and 0À05 to 59À5 parts by weight of an olefin polymer, and optionally up to 49À5 parts by weight of an ethylenically unsaturated compound until a homogeneous plastic is formed. Specified olefin polymers are polymers and copolymers of ethylene, propylene, butene, isobutene, pentenes, hexenes, heptenes and octenes. The dithiol polysulphide may be of formula where m is 0 to 17, R and R 1 are hydrogen or alkyl and p is at least 2; and may be prepared by reaction of a haloepoxy alkane, e.g. 1-chloro- 5,6 - epoxyhexane, 2 - chloro - 5,6 - epoxyhexane, 1 - chloro - 4,5 - epoxypentane, 1- chloro - 3,4 - epoxybutane, 2 - bromo - 3,4- epoxybutane, 1 - chloro - 2,3 - epoxybutane and 1 - chloro - 2,3 - epoxypropane, with hydrogen sulphide and an alkali or alkaline earth metal polysulphide in aqueous solution. Specified unsaturated compounds are isobutene, diisobutene, triisobutene, cyclopentene, cyclohexene, pinene, camphene, allo-ocimene, myrcene, styrene, a-methylstyrene, chlorostyrene, indene, allene, butadiene, isoprene, chloroprene, hexadiene-1,5, diallyl, dimethallyl, heptadiene- 1,6, cyclopentadiene, vinyl cyclopentadiene, vinyl cyclohexene, divinyl acetylene, divinyl benzene, trivinyl benzene and hexatriene. The products may be formed by the separate or simultaneous addition of the organic reactants to molten sulphur, or by prereacting the dithiol polysulphide with the unsaturated compound and optionally the sulphur. The products may be used for making traffic signs and, optionally mixed with sand or gravel, for covering ground. They may be used in paints and as a jointing medium. Examples describe (I) the preparation of a dithiol polysulphide by reacting sodium hydroxide, sulphur, hydrogen sulphide and epichlorohydrin; and the preparation of plastic compositions by reacting this product with sulphur and (II) polybutene, (III and VIII) polybutene and styrene, (VI) polyethylene, (IX and X) polyisobutylene and styrene, (XI) ethylene/propylene copolymer and a-methylstyrene, (XII) atactic polypropylene and (XIII) atactic polypropylene and chloroprene. | ||||||
186 | Curing of liquid polysulfide polymers | US56537466 | 1966-07-15 | US3389106A | 1968-06-18 | SIMPSON BILLY D |
187 | Sealed structures and process therefor | US47698765 | 1965-08-03 | US3348351A | 1967-10-24 | LOUIS CITAREL; GIORDANO JOSEPH J |
188 | High rank polysulfide polymers, process and products | US58348066 | 1966-09-30 | US3331818A | 1967-07-18 | BERTOZZI EUGENE R |
189 | Polysulfide polymers | US30007963 | 1963-08-05 | US3305536A | 1967-02-21 | WARNER PAUL F |
190 | Production of polyhaloalkyl sulfenyl chlorides | US15481061 | 1961-11-24 | US3169104A | 1965-02-09 | PACINI HARRY A; PAVLATH ATTILA E; FOLEY JR WILLIAM M |
191 | Polymers of dimercaptobicyclo-[2.2.1] heptanes and sulfur | US80307959 | 1959-03-31 | US3037967A | 1962-06-05 | LOUTHAN RECTOR P |
192 | Process for making polysulfide liquid polymers | US57977356 | 1956-04-23 | US2919262A | 1959-12-29 | NUMMY WILLIAM R |
193 | Diglycidyl thioethers of dithiols containing oxygen preparation and reaction products | US35202453 | 1953-04-29 | US2731437A | 1956-01-17 | BENDER HOWARD L; FARNHAM ALFORD G; GUYER JOHN W |
194 | Polysulfide polymers | US31714752 | 1952-10-27 | US2728748A | 1955-12-27 | DAVIS FRANKLIN O |
195 | Method of polymerizing polyalkylene polysulfides | US32699052 | 1952-12-19 | US2727883A | 1955-12-20 | BARTH WALTHER L A |
196 | Polysulfide polymer reaction and product | US21347551 | 1951-03-01 | US2606173A | 1952-08-05 | FETTES EDWARD M |
197 | Organopolysulfide rubber | US47896343 | 1943-03-12 | US2411275A | 1946-11-19 | KINNEBERG IVAR H; THOMAS CHARLES L |
198 | Polysulphide copolymer | US33907540 | 1940-06-06 | US2363615A | 1944-11-28 | PATRICK JOSEPH C |
199 | Coating and impregnating medium | US42885220 | 1920-12-07 | US1663160A | 1928-03-20 | CARLETON ELLIS |
200 | 加工性に優れたポリアリーレンスルフィド、及び製品 | JP2017018847 | 2017-02-03 | JP6425315B2 | 2018-11-21 | パク ギュテ; キム スンギ; イム ジェボン; チャ イルフン; イ セホ |