詳細內容：PA6 PX08000┘PA6 PX08000 PVC天津大沽化工P450 POM 日本寶理 YF-5 BK PC日本三菱工程 GS2020MKR TPV 美國AES 223-50 TPV 日本三井化學 8051BS MS新加坡電氣化學TX-100S SEBS中石化巴陵YH-604 HDPE菲律賓NPC AHD6070UA TPE德國膠寶TC6MGA PP中石化茂名BMT25S PA612美國杜邦FE3734 PP臺塑FPD943 PA6瑞士EMS RDS 4543 PC韓國LG 1301V-10 ABS日本住友化學GA-501 PP韓國油化HJ4045 PEI 基礎創(chuàng)新塑料 EL003 PP韓國SK RX5200 TPU德國巴斯夫C98A PP李長榮6524 PP沙特681K PA6日本東麗CM1011G-30 BK PBT廣州LGGP2306FW PC臺化 AC2821-ANPPO 基礎創(chuàng)新塑料 GFN2 TPUE-385AL TPEE日本東麗7247 TPE蘇州吉力士G7670-1 PVDF 上海三愛富 FR921-1 PC/PET 德國科思創(chuàng)（拜耳） UT408 PP韓國大林EP640T POM 寶理 TD-5MT PA4T 荷蘭DSM XS85 PEI 基礎創(chuàng)新塑料 EX08318C-NC PBT基礎創(chuàng)新塑料420SEO-1001 PA6 PX08000┘PA6 PX08000 PA6 PX08000┘PA6 PX08000 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 PX08000┘PA6 PX08000 PP北歐化工HL504FB PBT歐盟杜邦T8O5 BK PBT馬來西亞寶理3105 PA66美國杜邦FN718 PBT德國朗盛B7425 PC上海三養(yǎng) 3025G20-NC PC德國科思創(chuàng)（拜耳） 1695 PC基礎創(chuàng)新塑料(南沙) 3412R PA9T 日本可樂麗 GN2450-1BK ABS日本UMGVW20 PA12 瑞士EMS TRV-4X9 PA66基礎創(chuàng)新塑料RB-100-10 PP韓國GSH710 POM 美國泰科納 S9243 PBT美國杜邦BM6450XD BK560 PC/ABS 廣州LG NS5000C PP寧波�；�石化S1003 PA66韓國羅地亞S60 G1 V30 PA6上海古比雪夫氮G50 NC201 POM/PTFE 日本寶理 YF-20 PA6T 德國巴斯夫 TKR4365G5 GPPS臺化GP5500 ABS日本住友化學H-050 PA66美國杜邦HTN53G50LRHF PP中石化廣州PPH-M14-G ABS基礎創(chuàng)新塑料AL001-WH7D317L PA66基礎創(chuàng)新塑料RCL-4036 TPUI-64D024A FEP 日本大金 NP20 PA66德國DOMO66ST4 PP李長榮PF7251 TPV 荷蘭DSM 3140N PA66上海羅地亞A 218 W V30 EVA臺聚UE632 TPV 美國埃克森美孚 9201-90 PA6 PX08000┘PA6 PX08000 PA6 PX08000┘PA6 PX08000 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 PX08000┘PA6 PX08000 PVC臺塑S-80 GPPS美國陶氏PS121 TPV 土耳其英菲力 V0-574-80A POM 韓國工程塑料 AF-11 PPS菲利普PR25(粉) POM 韓國可隆 EL304 LCP日本寶理T3B16A1 PMMA 日本旭化成 G800 AS(SAN)奇美PN-117H PEEK 英國威格斯 150G PP中石化上海M850B ABS日本A LGA-110G30 電木粉 日本住友化學 PM-9820 PC/ABS 基礎創(chuàng)新塑料 EXTC8081PP美國泰科納GF20-02 EVOH 日本合成化學 G25HC PA6德國巴斯夫A3KIXEF 美國蘇威 1002/0008 PA6日本三菱工程ST220 POE瑞士陶氏PL-1880G LCP美國伊士曼LG441 POM 日本旭化成 Z4520 PA12 德國贏創(chuàng)德固賽 E55S3 POM 日本寶理 DW-03A PP韓國韓華道達爾BI970 LLDPE泰國陶氏488-4A POM 美國杜邦 DE7057 PP中石化廣州CJS700-02 MBS日本鐘淵B-513 PP新加坡聚烯烴FC9412L PA66羅地亞A 246 M PC韓國LG LD7750 PBT基礎創(chuàng)新塑料(日本)PDR4922 BK TPV 土耳其英菲力 VU424-50A LDPE中石化茂名828A PA6 PX08000┘PA6 PX08000 PA6 PX08000┘PA6 PX08000 (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