序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
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.
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.
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
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