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Catalyzing carbonization function of ferric chloride based on acrylonitrile-butadiene-styrene copolymer/organophilic montmorillonite nanocomposites

机译:基于丙烯腈-丁二烯-苯乙烯共聚物/亲有机蒙脱土纳米复合材料的氯化铁催化碳化功能

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摘要

A study on the Lewis acids-type transition metal chloride (FeCl_3) catalyzing carbonization based on acrylonitrile-butadiene-styrene copolymer (ABS)/organophilic montmorillonite (OMT) nanocomposites has been achieved. The results of XRD, TEM and HREM experiments show the formation of intercalated structure. The thermal stability of the nanocomposites slightly decreases, but the char residue remarkably increases compared with pure ABS. Meanwhile, it is found that the loading of FeCl_3 leads to crosslinking of ABS, promotes the charred residue yield and catalytic graphitization effect. The structure and morphology (XRD, HREM, SAED and LSR) of the purified char residue approve further the presence of graphite sheets. The possible catalyzing carbonization mechanism is composed of three prominent aspects. The first is the catalyzing effect of FeCl_3 promoting the crosslinking of polymer. The second is the Hofmann degradation of OMT, whose degraded products have opposite role in promoting crosslinking reactions and the last is the nano-dispersed clay layers. The gas barrier properties of clay stop or reduce the release of the pyrolytic products, which have been dehydrogenated for more time and aromatized to form char.
机译:基于丙烯腈-丁二烯-苯乙烯共聚物(ABS)/有机蒙脱土(OMT)纳米复合材料,对路易斯酸型过渡金属氯化物(FeCl_3)催化碳化进行了研究。 XRD,TEM和HREM实验结果表明形成了插层结构。纳米复合材料的热稳定性略有下降,但与纯ABS相比,炭渣的残留量显着增加。同时,发现FeCl_3的负载导致ABS的交联,提高了焦化残渣的产率和催化石墨化效果。纯化的焦渣的结构和形态(XRD,HREM,SAED和LSR)进一步证实了石墨片的存在。可能的催化碳化机理包括三个主要方面。首先是FeCl_3促进聚合物交联的催化作用。第二个是OMT的霍夫曼降解,其降解产物在促进交联反应中具有相反的作用,最后一个是纳米分散的粘土层。粘土的阻气性可以阻止或减少热解产物的释放,而热解产物已经脱氢了更多的时间,并芳香化形成了焦炭。

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