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详细内容:PA6 PF00A↑PA6 PF00A PA66法国罗地亚A216V15 PPO 基础创新塑料(南沙) PVX1201 PA6日本三菱工程1013G10 TPE苏州吉力士OM6258-1 PP韩国油化RB4302 PA66日本旭化成FR250 EVA台聚UE3330 PP韩国SK BX3910 PA66美国泰科纳GF40-01 PA612 美国杜邦 158 PBT漳州长春3045-104E PA66美国首诺R513H TPU美国亨斯迈98AE PC基础创新塑料 EXL1414B PA11 法国阿托菲纳 M-BMN PPO 日本三菱工程 GX1100 BK LCP美国杜邦ZE16103 WT010 LCP日本东丽L204G35E PVDF 法国阿科玛 Kynar 461 PA66美国杜邦FE5382 POM 美国泰科纳 M450 PPS菲利普R-4-XT PA6德国巴斯夫B29HM01 PC比利时科思创(拜耳) 2097 PP中石化茂名PPH-T03 LCP日本住友化学SZ6506HF-B PC德国科思创(拜耳) 1897 HDPE沙特SABICF00952 PPO 基础创新塑料 WCD801A COC德国TOPAS 6013L-17 TPEE美国杜邦DYM350 BK PA6基础创新塑料PB1006 LM BN 70745 LLDPE中石化茂名DFDA-7042(粉) POM 日本旭化成 3010 ABS台化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韩国LG GP-2200 BK POM 德国赫斯特 C9021 LS PP日本PBC6D POM 美国泰科纳 TX90 PA612 基础创新塑料 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 韩国阿科玛 V040 PC日本出光 LC1200PURE PP北欧化工HH450FB PP上海乐天化学G-153 PC美国陶氏 303-10 TPEE日本东丽7247W KG235 POM 泰国三菱工程 F20-02 PA6/66美国杜邦72G33W NC010LLDPE台塑3224 PBT长春5630-276VFEP 金华永和 EW-5 TPU德国巴斯夫ESP 9368 PA9T 日本可乐丽 TZ101 POM 马来西亚宝理 M90 PBT日本宝理3105A PP新加坡聚烯烃FL9413G TPV 美国埃克森美孚 251-85W232 LDPE惠州中海壳牌2426H PA66德国巴斯夫A3WG5 NC TPV 美国埃克森美孚 123-40 PA66基础创新塑料RF-700-10 EM HS PC/ABS 沙伯基础 CX2244ME TPU美国陶氏101 PA66瑞士EMS AS/10 VO NC PA6日本东丽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镇江奇美D-120 TPU上海巴斯夫1185A PC/ABS 德国科思创(拜耳) T65 PA66基础创新塑料RCL-4536PC韩国三星 GW-3130 PP台塑5020 PA66深圳东丽CM3004G20 TPEE韩国可隆KP3339UM LCP日本住友化学E5008LEMA法国阿科玛14MGC02 PA6惠州南亚2210G6 EBK1 PBT漳州长春4130-202F TPU拜耳优得UD-71DU10 PP台化K8002 LCP日本东丽L204G40 TPE德国胶宝TF9MAA-S340PC韩国三养 3025U POM 宝理 M90CA LDPE惠州中海壳牌2426H ABS奇美PA-777B PBT惠州南亚1512 PPS菲利普R-4-280NA TPU美国路博润58315 PA66上海巴斯夫A3EG6 BK00564 POM 日本巴斯夫 N2211PVX PMMA 韩国LG H1334 PA9T 日本可乐丽 GP2450NH PPO 基础创新塑料 V0150B PC/ABS 美国陶氏 7560 BK PA12 德国赢创德固赛 L1743 PA66韩国可隆KN3322VO PFA 日本大金 AC-5820 PEI 基础创新塑料 EFL-4036 TPV 美国埃克森美孚 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
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