废塑料混合物分段热裂解的研究

在实验室研究了废塑料聚氯乙烯、聚乙烯、聚丙烯和聚苯乙烯在不同温度段内的热裂解特性 ,并对这些废塑料混合物进行了分段热裂解。结果表明 ,在 180～ 32 0℃温度段 ,可脱除聚氯乙烯中的HCl;在 32 0～ 36 0℃温度段聚苯乙烯进行热裂解 ;在 36 0～ 40 0℃温度段聚丙烯进行热裂解 ,聚氯乙烯进行第二步热裂解 ;40 0～ 5 0 0℃温度段聚乙烯进行热裂解。据此 ,在不同温度段可获得具有较高价值的化工原料苯乙烯单体、轻质燃料油和重质燃料油 ,达到合理回收利用的目的。

Effects of two modification methods on the mechanical properties of wood flour/recycled plastic blends composites: addition of thermoplastic elastomer SEBS-g-MAH and in-situ grafting MAH

The effect of maleic anhydride grafted styrene-ethylene- buty-lene-styrene block copolymer （SEBS-g-MAH） and in-situ grafting MAH on mechanical, dynamic mechanical properties of wood flour/recycled plastic blends composites was investigated. Recycled plastic polypro-pylene （PP）, high-density polyethylene （HDPE） and polystyrene （PS）, were mixed with wood flour in a high speed blender and then extruded by a twin/single screw tandem extruder system to form wood flour/recycled plastic blends composites. Results show that the impact properties of the composites were improved more significantly by using SEBS-g-MAH compatibilizer than by using the mixtures of MAH and DCP via reactive blending in situ. However, contrary results were ob-served on the tensile and flexural properties of the corresponding com-posites. In General, the mechanical properties of composites made from recycled plastic blends were inferior to those made from virgin plastic blends, especially in elongation break. The morphological study verified that the interfacial adhesion or the compatibility of plastic blends with wood flour was improved by adding SEBS-g-MAH or in-situ grafting MAH. A better interfacial bonding between PP, HDPE, PS and wood flour was obtained by in-situ grafting MAH than the addition of SEBS-g-MAH. In-situ grafting MAH can be considered as a potential way of increasing the interfacial compatibility between plastic blends and wood flour. The storage modulus and damping factor of composites were also characterized through dynamic mechanical analysis （DMA）.

Utilization of Hydrocarbons Obtained by Waste Plastic Pyrolysis： Energetic Utilization （Part Ⅰ）

The pyrolysis of different waste polymers （polyethylene, polypropylene and polystyrene） was investigated in a tube reactor at 550 ℃ in the absence of oxygen. Additionally the energetic utilization of products have also been followed both in refining and petrochemical industry. Pyrolysis products were separated into fractions of gases, naphtha, middle distillates and heavy oil. Raw materials have been collected both from industrial and household sources： polyethylene from agriculture, polyethylene from packaging and polystyrene from packaging and electronic equipments. Yields and properties of volatile products have changed by the raw materials. Products have been analyzed by gas chromatography. Fourier transformed infrared spectroscopy, size exclusion chromatography and other standardized methods. Naphtha had high octane numbers （80 〈 RON）, while high cetane numbers （〉 75） in case of middle distillates. Moreover fractions contained approximately half of unsaturated hydrocarbons, mainly α-olefins, but the percentage was depending on the raw materials. These properties are advantageous for fuel-like applications.

Utilization of Hydrocarbons Obtained by Waste Plastic Pyrolysis： Application for Additive Production （Part Ⅱ）

New route of the utilization of products obtained by waste plastic pyrolysis has been investigated. ct-olefin-succinic-anhydride intermediate based on new experimental additives has been developed and used for achieving the better properties of carbon fibre reinforced polymer composites. Hydrocarbon fractions were produced by the pure thermal pyrolysis of waste polymers in a tube reactor using 550 ℃ in the absence of oxygen. Selected compounds （C30-C50） from pyrolysis products have been used as raw materials in the additive synthesis step. Polymer composite specimens have been investigated among others by universal tensile machine, SEM （scanning electron microscopy） and FTIR （fourier transformed infrared spectroscopy） methods. The tensile strength could be increased by 29.9%, the E-modulus by 24.2% and the Charpy impact strength by 13.3% in the presence of the experimental additive. Fibre-matrix interaction has been studied on SEM micrographs of the fractured face of composites. The results of mechanical testes have been supported by the SEM micrographs and possible shames of the coupling have been proposed.

Production and closed-loop recycling of biomass-based malleable materials

The search of biomass-based substitutes for fossil-based plastics has become a pressing task due to the severe long-term threats of plastic wastes to the ecosystem.However,the development in this area is strongly impeded by the high cost of biomass separation and the poor processability of unseparated biomass.Herein,we demonstrate,for the first time,an efficient and scalable method to generate greener plastics by directly integrating unseparated biomass waste(i.e.,wood powder)with crosslinked covalent adaptable networks.Through a simple compression molding process,the wood biomass and polymer particles can be fused together to form a continuous material,which is endowed with repairability,reprocessibility,and closed-loop full recyclability.The method demonstrated in this work paves the way for largescale industrial production of environmentally friendly biomass-based plastics.