詳細內容：PA6 K240-HP┇PA6 K240-HP EVA韓國韓華2315 TPV 美國�？松梨� 201-64W175 ABS韓國LGTR-300 PA66深圳杜邦70G50HSLR BK TPU美國諾譽58213 POM 韓國工程塑料 F20-03 BK PPO 日本旭化成 300V-A1A3301 PC/ABS 廣州LG GP-5006AF PA6日本東麗CM1017XL2PC日本三菱工程 EGN-2020KR TPV 美國埃克森美孚 141-55 BK EVA巴西BraskemTN 2020 PC基礎創(chuàng)新塑料 DMX2415 PC基礎創(chuàng)新塑料(南沙) 925AU-116 PP臺灣福聚SJ3032 PBT臺灣南亞1400G6 PP韓國樂天化學JM-370 PVDF 法國蘇威 6020 PA66美國杜邦HTN51G35HSLR PC韓國LG GN-2201FM BK MBS美國羅門哈斯EXL-2620 TPV 荷蘭DSM 3150N TPEE荷蘭DSM 38D PP臺灣福聚PD-943 PPS日本東麗A610MG1 PA66基礎創(chuàng)新塑料RN001 BK1B599BZDD HIPS韓國巴斯夫495F GY ABS鎮(zhèn)江奇美D-150 PA46日本DSM TS271A1 PP沙特拉比格石化AW161 PBT臺灣長春4830BKF/NCF TPV 美國�？松梨� 251-80 P9H803 PC日本出光 G-2520 BK PA66日本宇部NAP2300B1 BK PA66日本東麗CM1017 PA6 K240-HP┇PA6 K240-HP PA6 K240-HP┇PA6 K240-HP 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 K240-HP┇PA6 K240-HP PA12 美國EMS LV-5H PC基礎創(chuàng)新塑料(西班牙) 940A-116 HDPE韓國韓華870F PA6荷蘭DSM K223-KMV6 TPU美國路博潤302EZ PA6德國巴斯夫B3U PBT漳州長春3020-104S PPO 日本旭化成 X533V 5X43315 PEEK 吉林中研高塑 770GL30 PC日本三菱工程 ECF2015R PA6美國舒爾曼GF45 LDPE基礎創(chuàng)新塑料(沙特)PC G80 HDPE韓國SK3301 PPO 日本旭化成 500V TPE荷蘭DSML-X07135 PA66日本東麗CM3004 PC基礎創(chuàng)新塑料(西班牙) 9945A PA6德國朗盛BKV30H2.0PC/ABS 基礎創(chuàng)新塑料 CX7259 PC日本高達 KG-20MRA PA66漳州長春20G6-104PA6廣東新會美達M2400 PA6德國巴斯夫B30SPOP美國陶氏1140G PA66河南神馬尼龍FYR27 PBT/PET 德國朗盛 ECOT3230 PVDF 美國蘇威 TA-BS110/0130 POE泰國陶氏7447 POM 韓國工程塑料 TS-25A ABS基礎創(chuàng)新塑料MG37EP-NA1000 PA6瑞士EMS BGZ-30/3 COC日本瑞翁790R AS(SAN)臺灣奇美PN-918 PC基礎創(chuàng)新塑料(南沙) D452-701 PC基礎創(chuàng)新塑料 DC-1002 EM FR ECO PA6 K240-HP┇PA6 K240-HP PA6 K240-HP┇PA6 K240-HP 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 K240-HP┇PA6 K240-HP ABS臺灣奇美PA-716 PA12 瑞士EMS TR-70 PEI 基礎創(chuàng)新塑料 CRS5001 ETFE 日本旭硝子 ZL522F（粉） PBT馬來西亞寶理2002 PBT漳州長春3030-200S PA12 基礎創(chuàng)新塑料 HF-1006 PEI 基礎創(chuàng)新塑料 EF1008 PVC韓國韓華EL-103 TPEE美國泰科納640 PBT漳州長春1100-600S EAA美國陶氏3440 PA6T 日本三井化學 E440NK TPU德國巴斯夫E1175A10 POM 日本寶理 M270-38 PC/ABS 美國盛禧奧（斯泰�。� 7570 ABS基礎創(chuàng)新塑料AL-4020 PBT基礎創(chuàng)新塑料VX5011 POM 日本三菱工程 FC2020H PA6德國巴斯夫B3M6 PPO 基礎創(chuàng)新塑料(南沙) V0150B PA66惠州南亞6210G9 FNC1 PBT美國杜邦LW9030 BK POE日本三井化學DF740 PMMA 法國阿科瑪 V 825-HID PP上海賽科K7926 TPV 美國�？松梨� 123-40 LCP日本住友化學E6006L ABS臺灣奇美PA-727 POM 深圳杜邦 23P PA66美國杜邦70G50HSLR PBT漳州長春3040-104 PEEK 基礎創(chuàng)新塑料 LC005 BK HDPE韓國LGME5000 LCP日本住友化學E6808LHF-BZ-Z PA6 K240-HP┇PA6 K240-HP PA6 K240-HP┇PA6 K240-HP (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