詳細內容：PA6 PF00A↑PA6 PF00A PA66法國羅地亞A216V15 PPO 基礎創(chuàng)新塑料(南沙) PVX1201 PA6日本三菱工程1013G10 TPE蘇州吉力士OM6258-1 PP韓國油化RB4302 PA66日本旭化成FR250 EVA臺聚UE3330 PP韓國SK BX3910 PA66美國泰科納GF40-01 PA612 美國杜邦 158 PBT漳州長春3045-104E PA66美國首諾R513H TPU美國亨斯邁98AE PC基礎創(chuàng)新塑料 EXL1414B PA11 法國阿托菲納 M-BMN PPO 日本三菱工程 GX1100 BK LCP美國杜邦ZE16103 WT010 LCP日本東麗L204G35E PVDF 法國阿科瑪 Kynar 461 PA66美國杜邦FE5382 POM 美國泰科納 M450 PPS菲利普R-4-XT PA6德國巴斯夫B29HM01 PC比利時科思創(chuàng)（拜耳） 2097 PP中石化茂名PPH-T03 LCP日本住友化學SZ6506HF-B PC德國科思創(chuàng)（拜耳） 1897 HDPE沙特SABICF00952 PPO 基礎創(chuàng)新塑料 WCD801A COC德國TOPAS 6013L-17 TPEE美國杜邦DYM350 BK PA6基礎創(chuàng)新塑料PB1006 LM BN 70745 LLDPE中石化茂名DFDA-7042(粉) POM 日本旭化成 3010 ABS臺化AT5500 PA6 PF00A↑PA6 PF00A PA6 PF00A↑PA6 PF00A 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. PA6 PF00A↑PA6 PF00A PC韓國LG GP-2200 BK POM 德國赫斯特 C9021 LS PP日本PBC6D POM 美國泰科納 TX90 PA612 基礎創(chuàng)新塑料 SF-1004-NC PPO 日本旭化成 220Z PBT杭州新光3803 HDPE沙特埃克森美孚HMA-025 PC日本三菱工程 GS3010SR-9001 PMMA 韓國阿科瑪 V040 PC日本出光 LC1200PURE PP北歐化工HH450FB PP上海樂天化學G-153 PC美國陶氏 303-10 TPEE日本東麗7247W KG235 POM 泰國三菱工程 F20-02 PA6/66美國杜邦72G33W NC010LLDPE臺塑3224 PBT長春5630-276VFEP 金華永和 EW-5 TPU德國巴斯夫ESP 9368 PA9T 日本可樂麗 TZ101 POM 馬來西亞寶理 M90 PBT日本寶理3105A PP新加坡聚烯烴FL9413G TPV 美國�？松�美孚 251-85W232 LDPE惠州中海殼牌2426H PA66德國巴斯夫A3WG5 NC TPV 美國埃克森美孚 123-40 PA66基礎創(chuàng)新塑料RF-700-10 EM HS PC/ABS 沙伯基礎 CX2244ME TPU美國陶氏101 PA66瑞士EMS AS/10 VO NC PA6日本東麗CM1011G-45 BK PA66集盛AFG30-FN00N1 PA6 PF00A↑PA6 PF00A PA6 PF00A↑PA6 PF00A 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. PA6 PF00A↑PA6 PF00A ABS鎮(zhèn)江奇美D-120 TPU上海巴斯夫1185A PC/ABS 德國科思創(chuàng)（拜耳） T65 PA66基礎創(chuàng)新塑料RCL-4536PC韓國三星 GW-3130 PP臺塑5020 PA66深圳東麗CM3004G20 TPEE韓國可隆KP3339UM LCP日本住友化學E5008LEMA法國阿科瑪14MGC02 PA6惠州南亞2210G6 EBK1 PBT漳州長春4130-202F TPU拜耳優(yōu)得UD-71DU10 PP臺化K8002 LCP日本東麗L204G40 TPE德國膠寶TF9MAA-S340PC韓國三養(yǎng) 3025U POM 寶理 M90CA LDPE惠州中海殼牌2426H ABS奇美PA-777B PBT惠州南亞1512 PPS菲利普R-4-280NA TPU美國路博潤58315 PA66上海巴斯夫A3EG6 BK00564 POM 日本巴斯夫 N2211PVX PMMA 韓國LG H1334 PA9T 日本可樂麗 GP2450NH PPO 基礎創(chuàng)新塑料 V0150B PC/ABS 美國陶氏 7560 BK PA12 德國贏創(chuàng)德固賽 L1743 PA66韓國可隆KN3322VO PFA 日本大金 AC-5820 PEI 基礎創(chuàng)新塑料 EFL-4036 TPV 美國�？松�美孚 201-64 PA6日本三菱工程1011CH5KR PA6 PF00A↑PA6 PF00A PA6 PF00A↑PA6 PF00A (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