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Pyrolysis of Household Plastic Wastes

机译:家用塑料废物的热解

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Aims: Thermal cracking of waste plastic (without catalyst) to useful chemicals.Study Design: To design the experimental procedure, we primarily concentrated on the thermal stability of the materials by bearing in mind the results of thermogravimetric analysis (TGA). Based on the thermogravimetric results the appropriate set-up for the decomposition of the plastic wastes was designed. Three common household plastic wastes – styrofoam dining plates (SDP), shipping protection styrofoam boxes (SPFB), and carrying plastic shopping bags (CPB) – were pyrolized into liquids. GC-MS was used to characterize the sample of the obtained liquids.Place and Duration of Study: The study was done in the Department of Biological and Physical Sciences at South Carolina State University (SCSU), Orangeburg, SC, USA, during the summer of 2012.Methodology: The thermal cracking process without catalyst was used to convert household waste plastics into liquids. Three types of waste plastics, SDP, SPFB and CPB were used for these studies. The waste plastics were cut into small slices suitable to fill the reactor. Prior to pyrolysis, the thermal stability of materials were determined by thermogravimetric analysis (from 70ºC to 650ºC) with a heating rate of 10ºC/min while the samples were purged with 10 mL/min argon. The condensed liquids were analyzed by a Shimadzu GC-MS model GCMS-QP 2010s using helium as the mobile phase.Results: The thermal stability of waste plastics depended on the nature of constituent polymers from which the plastic originated, as was expected. Polystyrene derivatives, SDP and SPFB, both physically soft and hard, had similar thermal stability. The highest decomposition rates were observed at temperatures 418ºC and 423ºC for soft and hard SPFB respectively. No leftover was observed by thermogravimetric analysis. SDP were thermally more stable than SPFB; the decomposition began around 400ºC. The highest weight loss rate was observed at 440ºC. The TGA leftover was about 3% of total mass of SDP. The bulk pyrolysis of SDP and SPFB had 20% to 30% leftover. The GC-MS chromatogram indicated that over 350 chemicals resulted from decomposition of polystyrene based materials; the most abundant compound of pyrolysis was styrene and styrene derivatives as expected. The pyrolysis of CPB yielded hydrocarbons C4 to C24 being both alkanes and alkenes as expected. The TIC picks of CPB were geminals; first being alkene and the next was alkane with the same number of carbons (Figure 9).Conclusion: The chemical composition of the liquids obtained and the yields depended on the original polymer, quality of the waste, and the engineering of thermolysis procedure. The refinement of liquids resulting from pyrolysis is necessary to obtain a quality fuel. The condensed liquids produced from pyrolysis contained highly reactive chemicals such as vinyl, alkene, and three- and four-member cyclic hydrocarbons, which make the storage life of these materials short. For long time storage, however, these liquids must be stabilized either by stabilizers or hydrogenation of the product promptly after collection.
机译:目的:废塑料(不带催化剂)热裂解成有用的化学物质。研究设计:为了设计实验程序,我们主要关注材料的热稳定性,同时牢记热重分析(TGA)的结果。根据热重分析结果,设计了用于分解塑料废料的适当装置。将三种常见的家用塑料废物-聚苯乙烯泡沫塑料餐盘(SDP),运输保护性聚苯乙烯泡沫塑料箱(SPFB)和携带塑料购物袋(CPB)-热解为液体。研究的地点和持续时间:这项研究是在夏季期间在美国南卡罗来纳州奥兰治堡的南卡罗来纳州立大学(SCSU)生物与物理科学系完成的:2012年。方法:采用无催化剂的热裂解工艺将家用废塑料转化为液体。这些研究使用了三种类型的废塑料SDP,SPFB和CPB。将废塑料切成小块以适合填充反应器。热解之前,通过热重分析(从70ºC到650ºC)以10ºC/ min的加热速率测定材料的热稳定性,同时用10 mL / min的氩气吹扫样品。通过Shimadzu GC-MS模型GCMS-QP 2010s使用氦气作为流动相分析了冷凝液。聚苯乙烯衍生物SDP和SPFB在物理上软硬都具有相似的热稳定性。对于软SPFB和硬SPFB,分别在418ºC和423ºC的温度下观察到最高的分解速率。通过热重分析未观察到残留物。 SDP比SPFB具有更高的热稳定性;分解开始于400ºC左右。在440ºC时观察到最高的失重率。 TGA剩余量约为SDP总质量的3%。 SDP和SPFB的本体热解剩余量为20%至30%。 GC-MS色谱图表明,聚苯乙烯基材料的分解产生了350多种化学物质。如所预期的,热解最丰富的化合物是苯乙烯和苯乙烯衍生物。 CPB的热解产生了预期的同时为烷烃和烯烃的烃C4至C24。 CPB的TIC精选是双子星。第一个是烯烃,第二个是碳原子数相同的烷烃(图9)。结论:获得的液体的化学组成和产率取决于原始聚合物,废物的质量和热解工艺的工程设计。热解产生的液体的精炼对于获得优质燃料是必要的。热解产生的冷凝液含有高反应性化学物质,例如乙烯基,烯烃以及三元和四元环状烃,这会使这些材料的储存寿命缩短。但是,对于长时间存储,必须在收集后立即通过稳定剂或产品氢化来稳定这些液体。

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