Study of a two steps process for the valorization of PVC-containing wastes

Published online 27 November 2012The presence of organic compounds in wastes, namely polymer based compounds, is considered a potential relevant source of energy. However, the presence of polyvinyl chloride (PVC) in their composition, causes recycling problems when a thermal process is considered for the wastes treatment [1] preventing its use on processes which the main goal is the energy recovery (Zevenhoven et al. in Fuel 81:507–510, 2002; Kim in Waste Manag 21:609–616, 2001). A possible solution should consider a first step for chlorine removal, through a pyrolysis process previously to a subsequent thermal treatment, for energetic valorization. The present work assesses a possible process for treating PVC-containing wastes in an environmentally friendly way. It is based on the effective de-chlorination of PVC-containing wastes through a pyrolysis process at low temperature before the carbonaceous residue (chlorine free fraction) being subjected to a subsequent thermal treatment for energetic valorization with the production of a synthesis gas (syngas). In the end of the process concentrated hydrochloric acid or other chlorine solutions and a syngas, with high energetic potential are obtained. The synthesis gas produced can be used in turbines or gas engines, replacing the gases obtained from fossil non-renewable resources. The validation of the proposed treatment of PVC-containing wastes in pilot scale has also been performed

Polyolefins reinforced with short vegetal fibers: sisal vs. curauá

There is growing interest in reinforced polymer composites using short vegetal fibers to replace glass fibers for several reasons. The composite fibers are produced from renewable resources, being biodegradable and less abrasive to the processing equipment, in addition to possessing a lower density than the glass fibers. Since their thermal degradation onset is at 200 °C, they can be used to reinforce thermoplastics processed below this temperature and thermosets. Several vegetal fibers have been used as reinforcing agent, including sisal and cuaruá. However, there is controversy in the literature about the composites final properties. In this work we compare the properties of composites of high density polyethylene or polypropylene with 20 wt. (%) of short sisal or curauá fibers, with or without a coupling agent. All composites were processed by extrusion and molded by injection, under exactly the same conditions, and the mechanical properties were compared. The curauá fibers presented a higher tensile resistance than the sisal fibers, and the composites with curauá fibers had slightly higher tensile and flexural resistance compared to the sisal fiber composites. The situation is opposite in the impact resistance results, with sisal composites displaying higher impact resistance. Since sisal fibers are more fragile than curauá fibers, during processing there is a higher fracture of sisal in comparison to curauá, inducing these differences in composites mechanical properties.É crescente o interesse nos compósitos poliméricos reforçados com fibras vegetais curtas em substituição às fibras de vidro, pois as fibras naturais provêm de fontes renováveis, não são abrasivas aos equipamentos de processamento, são biodegradáveis, e possuem baixa densidade comparada às fibras de vidro. Elas apresentam início de degradação em torno de 200 °C, sendo adequadas para reforçar poliolefinas que são processadas até essa temperatura ou termofíxos. Várias fibras vegetais vêm sendo usadas como reforço, dentre elas o curauá e o sisal; no entanto, há grande controvérsia na literatura sobre as propriedades finais dos compósitos. Neste trabalho comparamos as propriedades de compósitos de polietileno de alta densidade ou polipropileno com 20% em massa de fibras curtas de sisal ou de curauá com ou sem agentes de acoplagem. Todos foram processados por extrusão e moldados por injeção, exatamente nas mesmas condições, e os resultados foram comparados em termos das propriedades mecânicas. As fibras de curauá apresentam resistência à tração superior às fibras de sisal e os compósitos com fibras de curauá apresentaram resistência à tração e flexão ligeiramente superior aos compósitos com fibra de sisal. No caso da resistência ao impacto a situação se inverte. Como o sisal é mais frágil que o curauá, durante o processamento ocorre maior quebra da fibra provocando essa diferenciação nas propriedades mecânicas dos compósitos.168174Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

Influência da fonte de carbono nas propriedades de híbridos Ni/Carbono preparados por carbonização hidrotérmica e tratamento térmico e utilizados como suportes para eletrocatalisadores PtRu/C

Neste trabalho, híbridos Ni/Carbono foram preparados em duas etapas (carbonização hidrotérmica e tratamento térmico a 900 °C sob argônio) a partir de diferentes fontes de carbono: glicose, amido e celulose. Eletrocatalisadores PtRu/C foram preparados pelo método da redução por álcool utilizando os híbridos como suportes. Os materiais foram caracterizados por espectroscopia por energia dispersiva de raios-X (EDX), análise termogravimétrica (TGA), espectroscopia no infravermelho com transformada de Fourier (FTIR), isotermas de B.E.T., difração de raios-X (DRX), microscopia eletrônica de transmissão (TEM) e voltametria cíclica em meio ácido. A eletro-oxidação do metanol foi estudada por cronoamperometria. O eletrocatalisador PtRu/C preparado utilizando o híbrido sintetizado a partir da celulose apresentou uma eletroatividade levemente superior aos demais materiais obtidos.Palavras-chave: Metanol. Célula a combustível. Carboidratos.

Ethanol oxidation activity and structure of carbon-supported Pt-modified PdSn-SnO2 influenced by different stabilizers

PdSn-SnO2 nanoparticles supported on Vulcan XC-72 carbon were synthesized by chemical reduction in the presence of three different stabilizing agents: ethylene diamine tetra-acetic acid (EDTA), sodium citrate (Nacitrate) and hexamethylenetetramine (HMTA). TEM analysis showed that PdSn-SnO2 /C catalyst made using the HMTA stabilizer produced the smallest particle size. XRD analysis detected the presence of PdSn alloy and the SnO2 phase in all three PdSn-SnO2 /C samples, and showed that PdSn-SnO2 (HMTA) had the smallest lattice parameter. After PdSn-SnO2 samples were modified by Pt, the particle size distribution and average size of nanoparticles of Pt-PdSn-SnO2 did not obviously change, and the fcc structure of PdSn in all three samples was retained. XPS measurement showed a higher upshift of Pt 4f binding energy occurred for Pt/PdSn-SnO2 /C (HMTA) compared to those of Pt/PdSn-SnO2 /C (EDTA) and Pt/PdSn-SnO2 /C (Nacitrate). Pt/PdSn-SnO2 /C (HMTA) was also found to have the highest CO and ethanol oxidation activity among the three catalysts.Web of Scienc