首页 / 国际专利分类库 / 化学;冶金 / 有机高分子化合物;其制备或化学加工;以其为基料的组合物 / 用碳-碳不饱和键以外的反应得到的高分子化合物 / 由在高分子主链上形成碳酸酯键的反应制得的高分子化合物(聚碳酸酯-酰胺类入C08G69/44; 聚碳酸酯-酰亚胺类入C08G73/16)
序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
101 Poly(carbonates) US664127 1976-03-05 US4079038A 1978-03-14 Nam Sok Choi; Jorge Heller
Poly(orthoester carbonates) and poly(orthocarbonate carbonates) having a repeating linear carbonate unit and a recurring symmetrical dioxycarbon moiety with a plurality of organic groups pendant from the carbon atom thereof are disclosed. The polymers are represented by the structural formula: ##STR1## WHEREIN A IS 0 TO 1, B IS 2 TO 6 WHEN A IS 0, B IS 2 TO 5 WHEN A IS 1, AND N IS GREATER THAN 10.
102 Copolymers of 1,2-dimethoxy-ethylene and .beta.-lactones or cyclic six-membered ring carbonates US414618 1973-11-08 US3976623A 1976-08-24 Norbert Vollkommer
A copolymer of 1,2-dimethoxy ethylene and a cyclic compound having an oxygen atom as a component of the chain, said copolymer having the formula: ##EQU1## wherein Y is a straight bond or --CH.sub.2 --O--, R.sup.1 and R.sup.2 are independently hydrogen or alkyl of 1-4 carbon atoms, n and m an integers n + m = 10 to 1,000; a process for such copolymers which comprises contacting 1,2 dimethoxy ethylene under copolymerization conditions with a cyclic organic compound having oxygen in the ring, said compound selected from the group consisting of .beta.-lactones and cyclic six-membered ring carbonates in the presence of an initiator in an amount between 0.1 and 10 mole percent based upon said 1,2-dimethoxyethylene and said cyclic organic compound, which initiator is of the group of halogen containing organoaluminum compounds having the formulaAl(R).sub.a X.sub.bWhereinR is a saturated aliphatic radical of from about 1 to 6 carbon atoms, or phenyl,X is chlorine or bromine,a + b are each 1, 1.5 or 2, the sum of a + b being 3.
103 Thermal oxidatively stable polycarbonate composition US3766139D 1971-07-29 US3766139A 1973-10-16 BIALOUS C; JAQUISS D
A THERMAL OXIDATIVELY STABLE POLYCARBONATE COMPOSITION CONSISTING OF THE REACTION PRODUCT OF BISPHENOL-A, A CARBONATE PRECURSOR AND A MINOR AMOUNT OF PHOSPHORUS DIHALIDE AND TO A PROCESS FOR PREPARING THE STABLE POLYMER COMPOSITION WHICH CONSISTS OF ADDING 0.0005 TO ABOUT 0.01 MOLE OF A PHOSPHORUS DIHALIDE PER MOLE OF BISPHENOL-A TO THE REACTION MEDIUM.
104 Hydrazine-carboxylic acid esters and process for the production thereof US3663603D 1968-03-12 US3663603A 1972-05-16 MULLER ERWIN; HEYDKAMP WOLFGANG
POLYHYDRAZINE-MONOCARBOXYLIC ACID ESTERS AND A PROCESS FOR THEIR PRODUCTION BY REACTING A POLYMONOPHENYL CARBONATE OF A POLYHYDRIC ALCOHOL WITH HYDRAZINE OR HYDRAZINE HYDRATE.
105 Orthoesters derived from glycerol US3644423D 1969-06-10 US3644423A 1972-02-22 ROSWELL DAVID F; KRAMM DAVID E; WOOD LOUIS L; STEADMAN THOMAS R
R''-(O-(2-R-1,3-DIOXOLAN-2,4-YLENE)-CH2)N-OH

WHERE R IS HYDROGEN OR LOWER ALKYL AND R'' IS LOWER ALKYL AND N IS AN INTEGER FROM 1-20 AND TO A METHOD FOR PREPARING SAID ORTHOESTER BY REACTING GLYCEROL WITH AN ORTHOESTER HAVING THE FORMULA R-C(OR'')3 WHERE R AND R'' ARE AS DEFINED SUPRA, ALL AS RECITED HEREINAFTER.
IN ABSTRACT, THIS INVENTION IS DIRECTED TO AN ORTHOESTER HAVING THE FORMULA

106 Branching or crosslinking of polycarbonates US3597394D 1969-10-16 US3597394A 1971-08-03 RAWLINGS HERBERT L
POLYCARBONATES ARE BRANCHED OR CROSSLINKED BY THE ADDITION OF THE CYCLIC TRIMER OF PHOSPHONITRILIC CHLORIDE.
107 Polycarbonates from bis-hydroxy(-alkyl and -aryl)pyromellitic diimides US3536670D 1969-05-26 US3536670A 1970-10-27 AELONY DAVID; COURY ARTHUR J
108 Process for preparing thermoplastic polycarbonates US3525712D 1965-09-01 US3525712A 1970-08-25 KRAMER MORTON
109 Vinyl polymer grafts on polycarbonates US3462515D 1967-01-17 US3462515A 1969-08-19 CANTRILL JAMES E
110 Process for the preparation of organic carbonic acid esters of polyhydroxy compounds containing isocyanato groups US3458475D 1966-06-10 US3458475A 1969-07-29 KRIMM HEINRICH; SCHNELL HERMANN
111 Non-crystallizable copolycarbonate/urethane resins prepared from 2, 2, 4, 4-tetraalkyl-1, 3-cyclobutanediol and a piperazine US51308665 1965-12-10 US3402150A 1968-09-17 GARDIKES JOHN J; MARKUS MATZNER
112 Thermosetting polyesters US13797661 1961-09-14 US3355414A 1967-11-28 CALDWELL JOHN R; JACKSON JR WINSTON J
113 Linear polyesters and polyester-amides from 2, 2, 4, 4-tetraalkyl-1, 3-cyclobutanediols US86037559 1959-12-18 US3313777A 1967-04-11 ELAM EDWARD U; MARTIN JAMES C; RUSSELL GILKEY
114 Polymers of cyclic carbonates US31167463 1963-09-26 US3301824A 1967-01-31 FRITZ HOSTETTLER; COX EUGENE F
115 Polycarbonates from diphenolic acids US6108260 1960-10-07 US3291774A 1966-12-13 BOLGIANO NICHOLAS C
116 Polycarbonate elastomers US23158962 1962-10-18 US3287442A 1966-11-22 CALDWELL JOHN R; JACKSON JR WINSTON J
117 Tri-bisphenol-a ester of phosphoric acid US20267362 1962-06-15 US3146254A 1964-08-25 BOOZALIS THEODORE S; MCKEEVER RICHARD B
118 Polychloroformates US1851060 1960-03-30 US3051686A 1962-08-28 BISSINGER WILLIAM E
119 Photographic filter and antihalation layers US67219957 1957-07-16 US3022171A 1962-02-20 ARMIN OSSENBRUNNER; HELFRIED KLOCKGETHER
120 ELECTRICALLY INSULATING THERMALLY CONDUCTIVE POLYMER RESIN COMPOSITION BASED ON STYRENICS WITH BALANCED PROPERTIES US15766143 2016-10-06 US20180291195A1 2018-10-11 Tobias SCHULZ; Norbert NIESSNER; Gisbert MICHELS; Janna MICHAELIS DE VASCONCELLOS; Hans-Werner SCHMIDT; Florian WIEBERGER; Tristan KOLB
Thermally conductive polymer (TCP) resin composition (i) or (ii) are described, comprising components (I) and (II): (i) 40 to 72% by volume of at least one matrix polymer (I); 28 to 60% by volume of a thermally conductive filler material (II) (D50 0.1 to 200 μm) consisting of aluminosilicate (II-1) in combination with a further component (II-2) selected from: multi wall carbon nanotubes, graphite and and boron nitride, wherein the volume ratio (ll-1)/(ll-2) is 30:1 to 0.1:1; or (ii) 40 to 65% by volume of at least one matrix polymer (I); 35 to 60% by volume of aluminosilicate (II) (D50 0.1 to 200 μm); wherein the matrix polymer (I) comprises styrenic polymers (I′) selected from: ABS resins, ASA resins, and elastomeric block copolymers. Shaped articles made thereof can be used as “Cool Touch” surfaces for automobile interior, motor housings, lamp housings and electrical and electronic housings and as heat sinks for high performance electronics or LED sockets.
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