首页> 外文期刊>Polymers for advanced technologies >Fluorosilicone elastomer based on the poly [(3,3,3-trifluoropropyl)methyl-siloxane-co-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)methylsiloxane]
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Fluorosilicone elastomer based on the poly [(3,3,3-trifluoropropyl)methyl-siloxane-co-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)methylsiloxane]

机译:基于聚[(3,3,3-三氟丙基)甲基硅氧烷-共-(3,3,4,4,5,5,6,6,6-九氟己基)甲基硅氧烷的氟硅氧烷弹性体]

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Fluorosilicone elastomer based on the poly[(3,3,3-tri-fluoropropyl) methylsiloxane-co-(3,3,4,4,5,5,6,6,6-nona-fluorohexyl) methylsiloxane] was studied. First, the synthesis of fluorosilicone polymer based on the poly[(3,3,4,4,5,5,6,6,6-nonafluorohexyl) methylsiloxane](PNFHMS) was examined by the polymerization of 1,3,5-tris(3,3,4,4,5,5,6,6,6-nonafluorohexyl)1,3,5-tri-methylcyclotrisiloxane (C{sub}4F{sub}9D3) by sodium hydroxide. On the contrast of the polymerization of the commercially available 1,3,5-tris(3,3,3-trifluoropuopyl)-1,3,5trimethyl-cyclotrisiloxane (CF{sub}3D{sub}3), the polymerization of C{sub}4F{sub}9D{sub}3 with sodium hydroxide resulted in the formation of 1,3,5,7-tetrakis(3,3,4,4,5,5,6,6,6-nonafluorohexyl)-1,3,5,7-tetramethylcyclotetrasiloxane:[C{sub}4F{sub}9CH{sub}2CH{sub}2(CH{sub}3)-SiO]{sub}4 (C{sub}4F{sub}9D4) as the major product. It was due to the easy occurrence of the depolymerization by the back-biting mechanism, because C{sub}4F{sub}9D4 is more stable than 1,3,5,7-tetrakis(3,3,3-trifluoropropyl)1,3,5,7-tetramethylcyclotetrasiloxane:[CF{sub}3CH{sub}2CH{sub}2(CH{sub}3)SiO]{sub}4 (CF{sub}3D4). The above result made us to conclude that it was difficult to apply the polymer based on PNFHMS to heat vulcanizable elastomers and to investigate the dlastomer based on the poly[(3,3,3-trifluoropropyl)-methylsiloxane-co-(3,3,4,4,5,5,6,6,6-nonafluorrhexyl)-methylsiloxane]. C{sub}4F{sub}9D3 and CF{sub}3D3 were copolymerized successfully by sodium hydroxide and formulated with the silica treated by CF{sub}3D3. The use of silica treated with methylsilyl unit failed, because creep-hardening phenomenon occurred. This elastomer was evaluated about some mechanical properties, and the resistance to organic solvents, and a fuel. The advantage that can be detected form the introduction of [C{sub}4F{sub}9C{sub}2H{sub}4-(CH{sub}3)SiO] unit was that the resistance to the polar solvents such as acetone and dimethylformamide was improved.
机译:研究了基于聚[(3,3,3-三氟丙基)甲基硅氧烷-共-(3,3,4,4,5,5,6,6,6-壬基-氟己基)甲基硅氧烷]的氟硅氧烷弹性体。首先,通过1,3,5-的聚合反应,研究了基于聚[(3,3,4,4,5,5,6,6,6,6-,6-九氟己基)甲基硅氧烷](PNFHMS)的氟硅氧烷聚合物的合成通过氢氧化钠制备三(3,3,4,4,5,5,6,6,6-九氟己基)1,3,5-三甲基环三硅氧烷(C {sub} 4F {sub} 9D3)。与市售的1,3,5-三(3,3,3-三氟puopyl)-1,3,5-三甲基-环三硅氧烷(CF {sub} 3D {sub} 3)的聚合形成对比。用氢氧化钠{sub} 4F {sub} 9D {sub} 3导致形成1,3,5,7-四(3,3,4,4,5,5,6,6,6-九氟己基) -1,3,5,7-四甲基环四硅氧烷:[C {sub} 4F {sub} 9CH {sub} 2CH {sub} 2(CH {sub} 3)-SiO] {sub} 4(C {sub} 4F { sub} 9D4)作为主要产品。这是由于通过咬合机制容易发生解聚,因为C {sub} 4F {sub} 9D4比1,3,5,7-四(3,3,3-三氟丙基)1更稳定,3,5,7-四甲基环四硅氧烷:[CF {sub} 3CH {sub} 2CH {sub} 2(CH {sub} 3)SiO] {sub} 4(CF {sub} 3D4)。上述结果使我们得出结论,难以将基于PNFHMS的聚合物应用于可热硫化的弹性体,也难以研究基于聚[(3,3,3-三氟丙基)-甲基硅氧烷-共-(3,3)的弹性体,4,4,5,5,6,6,6-九氟己基)-甲基硅氧烷]。 C {sub} 4F {sub} 9D3和CF {sub} 3D3通过氢氧化钠成功共聚,并与CF {sub} 3D3处理的二氧化硅一起配制。使用甲基甲硅烷基单元处理的二氧化硅失败,因为发生了蠕变硬化现象。评价该弹性体的一些机械性能,对有机溶剂和燃料的抗性。通过引入[C {sub} 4F {sub} 9C {sub} 2H {sub} 4-(CH {sub} 3)SiO]单元可以检测到的优点是对极性溶剂(例如丙酮)的耐受性改善了二甲基甲酰胺。

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