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Nanostructured Synthetic Carbons Obtained by Pyrolysis of Spherical Acrylonitrile/Divinylbenzene Copolymers

机译:由球形丙烯腈/二乙烯基苯共聚物的热解获得的纳米结构的合成炭

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摘要

Novel carbon materials have been prepared by the carbonization of acrylonitrile (AN)/divinylbenzene (DVB) suspension porous copolymers having nominal crosslinking degrees in the range of 30–70% and obtained in the presence of various amounts of porogens. The carbons were obtained by pre-oxidation of AN/DVB copolymers at 250−350°C in air followed by pyrolysis at 850°C in an N2 atmosphere. Both processes were carried out in one furnace and the resulting material needed no further activation. Resulting materials were characterized by XPS and low temperature nitrogen adsorption/desorption. It was found that maximum pyrolysis yield was ca. 50% depending on the oxidation conditions but almost independent of the crosslinking degree of the polymers. Porous structure of the carbons was characterized for the presence of micropores and macropores, when obtained from highly crosslinked polymers or polymers oxidized at 350°C and meso- and macropores in all other cases. The latter pores are prevailing in the structure of carbons obtained from less porous AN/DVB resins. Specific surface area (BET) of polymer derived carbons can vary between 440 m2/g and 250 m2/g depending on the amount of porogen used in the synthesis of the AN/DVB polymeric precursors.
机译:新型碳材料是通过将标称交联度在30-70%范围内的丙烯腈(AN)/二乙烯基苯(DVB)悬浮多孔共聚物碳化而制备的,并且是在存在各​​种成孔剂的情况下获得的。碳是通过在空气中250-350°C下对AN / DVB共聚物进行预氧化,然后在N2气氛中在850°C下热解而获得的。两种方法均在一炉中进行,所得材料无需进一步活化。所得材料通过XPS和低温氮吸附/解吸进行表征。发现最大的热解产率为约。 50%取决于氧化条件,但几乎与聚合物的交联度无关。当从高度交联的聚合物或在350°C下氧化的聚合物以及中孔和大孔获得的所有其他情况下,碳的多孔结构表征为存在微孔和大孔。从孔较少的AN / DVB树脂获得的碳结构中,后一种孔占主导。聚合物衍生碳的比表面积(BET)可以在440 m 2 / g和250 m 2 / g之间变化,具体取决于合成碳的成孔剂的量。 AN / DVB聚合物前体。

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