PA66 7023>PA66 7023

詳細內(nèi)容：PA66 7023>PA66 7023 ABS德國巴斯夫2812TR PMMA 韓國LG HP-202 PVC寧波臺塑S-60(粉） PA66基礎(chǔ)創(chuàng)新塑料RFL36SXD PA612 基礎(chǔ)創(chuàng)新塑料 IF1006 PA46荷蘭DSM TW275F6 PP中石化揚子PPB-M02-VPOM 美國杜邦 8102 PP中石化廣州J-640 PA66德國AKROA3GF301 ABS日本UMGVW803 PC基礎(chǔ)創(chuàng)新塑料(南沙) 925-701 PC日本三菱工程 GS2010MLR ABS廣州LGSE-750 BK TPV 美國埃克森美孚 9101-80E TPU美國路博潤GP 60 DB PA9T 日本可樂麗 GW2458PC/ABS 德國科思創(chuàng)（拜耳） FR3000 SEBS臺橡6152 LCP日本寶理E140I BK210JP PVDF 日本吳羽 W#7300(粉) PP中石油錦西1102K PPO 日本三菱工程 GX1210 BK SEBS美國科騰G-1780 SURLYN美國杜邦A(yù)M7927 PPS深圳東麗A400M XO5 PA612 美國杜邦 158L ETFE 日本旭硝子 ZL520N(粉) PP韓國樂天化學(xué)J-570S PP德國巴塞爾Q300F TPE美國杜邦5556 PA66法國羅地亞A216 S30 TPE美國道康寧G80A 41 PETG 韓國SK JN120 PPO 基礎(chǔ)創(chuàng)新塑料 WCD801A PA66 7023>PA66 7023 PA66 7023>PA66 7023 PVC PVC as early as 1835 for the United States V. Regnaud found, generating a white solid with sunlight of vinyl chloride, namely pvc. PVC was found two times in nineteenth Century, one was Henri Victor Regnault in 1835, and the other was found in 1872 by Eugen Baumann. In the two opportunity, the polymer appeared in a beaker of vinyl chloride placed under the light of the sun and became a white solid. In the early twentieth Century, Russian chemist Ivan Ostromislensky and chemist Fritz Klatte of Griesheim-Elektron company tried to use PVC for commercial purposes, but the difficulty was how to process this hard, sometimes brittle polymer. In 1912, the German Fritz Klatte synthesized PVC and applied for a patent in Germany, but was not able to develop a suitable product before the patent expired. In 1926, the Waldo Semon of the B.F. Goodrich company in the United States synthesized PVC and applied for a patent in the United States. Waldo Semon and B.F. Goodrich Company developed the method of plasticizing PVC by adding various auxiliaries in 1926, making it a more flexible and more easily processed material, and soon it was widely used in commercial applications. In 1914, organic peroxide could be used to accelerate the polymerization of vinyl chloride. In 1931, the German company adopted the emulsion polymerization process to realize the industrial production of PVC. In 1933, W.L. Simon proposed that the mixture of high boiling point solvents and three cresol phosphate can be mixed with PVC to produce soft PVC products, which has made a breakthrough in the practicability of PVC. The processing and application of suspended British Imperial Chemical Industries Limited, Union Carbine Co and goodride chemical company almost simultaneously in 1936 developed the polymerization of vinyl chloride and PVC. In order to simplify the production process, reduce energy consumption, in 1956 the French Shenggebang company developed bulk polymerization. In 1983, the world's total consumption was about 11.1Mt, and its total production capacity was about 17.6Mt. It was the second largest plastic product after polyethylene production, accounting for 15% of the total output of plastics. The self-designed PVC production plant in China was trial manufactured in Jinxi chemical plant of Liaoning in 1956. In 1958, the 3kt plant was formally industrialized and the output of 530.9kt was 1984. PA66 7023>PA66 7023 TPUI-64D024A PA66南亞6210G9 ABS基礎(chǔ)創(chuàng)新塑料EX58F-NA1000 TPE美國 APEXUN-7010-55 PVC臺塑PR-F PC日本三菱工程 DE2140UVR PBT美國杜邦SK652FR1 NC010 PC/ABS 德國科思創(chuàng)（拜耳） FR86- PC德國科思創(chuàng)（拜耳） 2207 PP韓國樂天化學(xué)DJ-560SPC/PET 基礎(chǔ)創(chuàng)新塑料 HX7509HP PBT新光E202G15 TPU美國路博潤UB450 LDPE北歐化工LE1120 TPU上海亨斯邁75AE PVDF 日本吳羽 W#7100(粉) PVC河北金牛SE-700 PA46日本DSM TS350 PA9T 日本可樂麗 GT2330 PVC德國S4099 POM 寶理 M90S PP廣州LG GP-3200 TPU德國科思創(chuàng)（拜耳）DP1485A PBT美國杜邦1830 FC TPU德國巴斯夫EB95A PC日本帝人 MN-3710S LLDPE加拿大諾瓦化學(xué)PI-2024A PA12 法國阿科瑪 MP1878 PC/ABS 基礎(chǔ)創(chuàng)新塑料 CX7720 ABS廣州LGHI-121H BK LLDPE上海賽科LL0209AA PC/ABS 寧波臺化 AC3108 PBT美國泰科納3316HR BK POE美國陶氏7256 PP新加坡聚烯烴Z451G PA66 7023>PA66 7023 PA66 7023>PA66 7023 PVC was industrialized in the early 30s. From 30s onwards, in a very long time, PVC production has been in the world of plastic content occupied the first. In the late 60s, polyvinyl chloride was replaced by polyvinyl chloride. Although PVC plastics are retreated to second, the output of PVC still accounts for more than 1/4 of the total plastic production. Before 60s, the production of mono vinyl chloride was mainly calcium carbide acetylene, because the production of calcium carbide consumed a large amount of electric energy and coke, high cost. At the beginning of the 60s ethylene oxychlorination process for vinyl chloride production industrialization, all countries turn to cheaper oil as raw material. In addition, most of the raw materials of PVC (about 57% wt%) are the associated by-products of chlorine, which are not only rich in raw materials, but also one of the most important products for developing chlor alkali industry and balancing chlorine. As a result, the proportion of PVC in plastic has been reduced, but it still maintains a high growth rate. PVC plastics products are widely used, but in the middle of 70s, it was recognized that the monomer vinyl chloride (VCM) remained in PVC resin and products is a serious EVA 1, widely used in foam material, functional films, packaging mold, hot melt adhesive, wire and cable and toys and other fields. 2, the EVA product of ethylene acetate content in 5%~10% is elastic film, etc. 3, the content of ethylene acetate is EVA in 20~28%, which is mainly used in hot melt adhesives and coating products. 4, the content of vinyl acetate is 5%~45%, the main products are thin film (including agricultural film) and sheet, injection molding, molded products, foaming products, hot-melt adhesives and so on. (1) foamed shoe material. The shoe material is the most important application field of EVA resin in our country. In the EVA resin used in the shoe material, the content of vinyl acetate is generally 15% ~ 22%. Because EVA resin blend foam is soft, elastic and chemical resistant, it is widely used in soles and interior materials of middle and high grade tourist shoes, mountaineering shoes, slippers and sandals. In addition, this material is also used in the field of sound insulation board, gymnastic mat and sealing material. (2) thin film. The main purpose of EVA film is the production of functional films. The functional films with high weatherability, anti fog and insulation performance, because polyethylene has no polarity, even adding a certain amount of antifogging agents, the antifogging properties can only be maintained for about 2 months; and adding a certain amount of EVA made of resin film, light not only has a higher rate, but also antifogging property have greatly improved, can be more than 4 months. In addition, EVA also can be used in the production of packaging film, medical film, laminated film, cast film. PA66 7023>PA66 7023 PC基礎(chǔ)創(chuàng)新塑料(南沙) ML7676 8A9D022 PP韓國大林HP500N PP臺塑5020 PPS美國赫斯特4665B6 OBC美國陶氏9000 LCP長春300B4G PBT日本東麗1101G-30 PA12 法國阿科瑪 MX1025 PA6德國巴斯夫100FR NC POM 日本寶理 EB-08 TPEE美國泰科納MT9647 LLDPE臺塑3840 PBT新光D202G30-4886 PC泰國三菱工程 FIN5000R PC/ABS 韓國LG HR-5007A TPV 美國埃克森美孚 241-80 LCP日本新石油化學(xué)MG350BPRL/PRL POM 德國泰科納 C9021 PC日本帝人 G-3115P PBT美國杜邦LW617 BK503 ABS韓國三星SD-0170W PA9T 日本可樂麗 TA104 ABS德國朗盛P2MC POM 德國赫斯特 C52021 BK PPS日本出光C-200SC PEEK 英國威格斯 150GL30 PPS深圳東麗A310MX04 AS(SAN)鎮(zhèn)江奇美D-178 LLDPE伊朗國家石化LL0209AA POM/PTFE 日本寶理 YF-10POM 德國巴斯夫 W2320-003 ABS高膠粉山東萬達WD-132 PC/ABS 廣州LG MP-5000AM ETFE 日本旭硝子 LM-730AP PC日本帝人 L-1225L PA66 7023>PA66 7023 PA66 7023>PA66 7023 (3) wire and cable. With the continuous development of computer and network engineering, more and more halogen-free flame-retardant cables and silane crosslinking cables are widely used due to the consideration of the safety of the computer room. Because EVA resin has good filler inclusiveness and crosslinkability, it is widely used in halogen free flame retardant cable, semiconductor shielded cable and two step silane crosslinking cable. In addition, the EVA resin is also used to make some special cable sheath. The EVA resin used in wire and cable is generally 12% to 24% of vinyl acetate. LCP1.1 advantages of material 2.2 material properties 3.3 molding process 4.4 main uses Material advantages LCP advantages. 1. High mobility 2. Good size and good stability 3. Good liquidity 4, solvent resistance 5. High mechanical strength 6. Combustibility LCP use. 1. Speed connectors, coils, switches, sockets 2. The parts of the pump and the parts of the valve 3. Automobile fuel peripheral parts 4, electronic furnace container Poor mechanical property perpendicular to the direction of idea and flow Material properties Nature Molding process