68 research outputs found

    Gasoline like fuel from plastic waste pyrolysis and hydrotreatment

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    Recycling of plastic waste is desirable to lower environmental pollution and fulfil the requirements of circular economy. Energetic utilization is another possibility, however, municipal solid waste containing plastics is usually combusted to generate heat and electricity. An attractive way of dealing with plastic waste is pyrolysis, which has the potential of producing liquid hydrocarbons suitable as a transportation fuel. The pyrolysis results of three plastics produced in the largest amount globally, namely polyethylene, polypropylene and polystyrene as well as their mixtures are presented. The experiments were performed in a laboratory scale batch reactor. The pyrolysis oils were further processed by distillation to provide gasoline and diesel like (distillation cuts at 210 and 350 °C) hydrocarbons. The gasoline fractions were analysed by GC-MS and the composition was compared with the EU gasoline standard. It was found that the oils from PE, PP and PS contain compounds present in standard gasoline. Mixing PS with PE and PP before the pyrolysis, or the oils afterward produces much closer results to standard requirements as PS pyrolysis generates mostly aromatic content. As standard maximizes the olefin content of gasoline to 18 Vol%, hydrogenation was also performed using Pd based catalyst. The hydrogenation process significantly reduced the number of double bonds resulting in low olefin content. Results show that the pyrolysis of plastic waste mixtures containing PE, PP and PS is a viable method to produce pyrolysis oil suitable for gasoline-like fuel extraction and further hydrogenation of the product can provide gasoline fuels with low olefin content

    Gasoline like fuel from plastic waste pyrolysis and hydrotreatment

    Get PDF
    Recycling of plastic waste is desirable to lower environmental pollution and fulfil the requirements of circular economy. Energetic utilization is another possibility, however, municipal solid waste containing plastics is usually combusted to generate heat and electricity. An attractive way of dealing with plastic waste is pyrolysis, which has the potential of producing liquid hydrocarbons suitable as a transportation fuel. The pyrolysis results of three plastics produced in the largest amount globally, namely polyethylene, polypropylene and polystyrene as well as their mixtures are presented. The experiments were performed in a laboratory scale batch reactor. The pyrolysis oils were further processed by distillation to provide gasoline and diesel like (distillation cuts at 210 and 350 °C) hydrocarbons. The gasoline fractions were analysed by GC-MS and the composition was compared with the EU gasoline standard. It was found that the oils from PE, PP and PS contain compounds present in standard gasoline. Mixing PS with PE and PP before the pyrolysis, or the oils afterward produces much closer results to standard requirements as PS pyrolysis generates mostly aromatic content. As standard maximizes the olefin content of gasoline to 18 Vol%, hydrogenation was also performed using Pd based catalyst. The hydrogenation process significantly reduced the number of double bonds resulting in low olefin content. Results show that the pyrolysis of plastic waste mixtures containing PE, PP and PS is a viable method to produce pyrolysis oil suitable for gasoline-like fuel extraction and further hydrogenation of the product can provide gasoline fuels with low olefin content

    Plastic waste treatment by pyrolysis

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    The influence of PET and PBT contamination during transportation fuel production via pyrolysis

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    The pyrolysis of plastic waste is a promising method to reduce waste accumulation while it could provide value-added transportation fuels. The main goal of this study is to investigate the influence of PET and PBT contamination during plastic pyrolysis oil production utilizing HDPE, LDPE, PP, and PS mixtures as these plastics are good candidates for transportation fuel production via pyrolysis and distillation. Seven different waste blends were prepared and pyrolyzed in a laboratory-scale batch reactor equipped with reflux. Mass balance, gas analysis, thermogravimetric analysis, and deposit formation were evaluated. It was concluded that by increasing the PET or PBT concentration in the initial solid waste mixtures, the oil production decreases while the amount of gases increases. Additionally, either PET or PBT generates operational difficulties due to they form deposits in piping system in form of benzoic acid. The maximum concentration of these plastic waste materials was 20% (PET) and 25% (PBT) in this study as further increase blocked the cross-section of piping, causing operational difficulties. Based on the obtained results the concentration of PET and PBT should be limited in waste mixtures when transportation fuel production is desired

    The influence of PET and PBT contamination during transportation fuel production via pyrolysis

    Get PDF
    The pyrolysis of plastic waste is a promising method to reduce waste accumulation while it could provide value-added transportation fuels. The main goal of this study is to investigate the influence of PET and PBT contamination during plastic pyrolysis oil production utilizing HDPE, LDPE, PP, and PS mixtures as these plastics are good candidates for transportation fuel production via pyrolysis and distillation. Seven different waste blends were prepared and pyrolyzed in a laboratory-scale batch reactor equipped with reflux. Mass balance, gas analysis, thermogravimetric analysis, and deposit formation were evaluated. It was concluded that by increasing the PET or PBT concentration in the initial solid waste mixtures, the oil production decreases while the amount of gases increases. Additionally, either PET or PBT generates operational difficulties due to they form deposits in piping system in form of benzoic acid. The maximum concentration of these plastic waste materials was 20% (PET) and 25% (PBT) in this study as further increase blocked the cross-section of piping, causing operational difficulties. Based on the obtained results the concentration of PET and PBT should be limited in waste mixtures when transportation fuel production is desired

    Differential recruitment of ventral pallidal e-types by behaviorally salient stimuli during Pavlovian conditioning

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    The ventral pallidum (VP) is interfacing striatopallidal and limbic circuits, conveying information about salience and valence crucial to adjusting behavior. However, how VP neuron populations with distinct electrophysiological properties (e-types) represent these variables is not fully understood. Therefore, we trained mice on probabilistic Pavlovian conditioning while recording the activity of VP neurons. Many VP neurons responded to punishment (54%), reward (48%), and outcome-predicting auditory stimuli (32%), increasingly differentiating distinct outcome probabilities through learning. We identified e-types based on the presence of bursts or fast rhythmic discharges and found that non-bursting, non-rhythmic neurons were the most sensitive to reward and punishment. Some neurons exhibited distinct responses of their bursts and single spikes, suggesting a multiplexed coding scheme in the VP. Finally, we demonstrate synchronously firing neuron assemblies, particularly responsive to reinforcing stimuli. These results suggest that electrophysiologically defined e-types of the VP differentially participate in transmitting reinforcement signals during learning. © 2021 The Author(s

    Lipid Regulation of the ABCB1 and ABCG2 Multidrug Transporters

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    This chapter deals with the interactions of two medically important multidrug ABC transporters (MDR-ABC), ABCB1 and ABCG2, with lipid molecules. Both ABCB1 and ABCG2 are capable of transporting a wide range of hydrophobic drugs and xenobiotics and are involved in cancer chemotherapy resistance. Therefore, the exploration of their mechanism of action has major therapeutic consequences. As discussed here in detail, both ABCB1 and ABCG2 are significantly affected by various lipid compounds especially those residing in their close proximity in the plasma membrane. ABCB1 is capable of transporting lipids and lipid derivatives, and thus may alter the general membrane composition by "flopping" membrane lipid constituents, while there is no such information regarding ABCG2. Still, both ABCB1 and ABCG2 show complex interactions with a variety of lipid molecules, and the transporters are significantly modulated by cholesterol and cholesterol derivatives at the posttranslational level. In this chapter, we explore the molecular details of the direct transporter-lipid interactions, the potential role of lipid-sensor domains within the proteins, as well as the application of experimental site-directed mutagenesis, detailed structural studies, and in silico modeling for examining these interactions. We also discuss the regulation of ABCB1 and ABCG2 expression at the transcriptional level, occurring through nuclear receptors involved in lipid sensing. The better understanding of lipid interactions with these medically important MDR-ABC transporters may significantly improve further drug development and clinical treatment options

    Mutations of the central tyrosines of putative cholesterol recognition amino acid consensus (CRAC) sequences modify folding, activity, and sterol-sensing of the human ABCG2 multidrug transporter

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    Human ABCG2 is a plasma membrane glycoprotein causing multidrug resistance in cancer. Membrane cholesterol and bile acids are efficient regulators of ABCG2 function, while the molecular nature of the sterol-sensing sites has not been elucidated. The cholesterol recognition amino acid consensus (CRAC, L/V-(X)(1-5)-Y-(X)(1-5)-R/K) sequence is one of the conserved motifs involved in cholesterol binding in several proteins. We have identified five potential CRAC motifs in the transmembrane domain of the human ABCG2 protein. In order to define their roles in sterol-sensing, the central tyrosines of these CRACs (Y413, 459, 469, 570 and 645) were mutated to S or F and the mutants were expressed both in insect and mammalian cells. We found that mutation in Y459 prevented protein expression; the Y469S and Y645S mutants lost their activity; while the Y570S, Y469F, and Y645F mutants retained function as well as cholesterol and bile acid sensitivity. We found that in the case of the Y413S mutant, drug transport was efficient, while modulation of the ATPase activity by cholesterol and bile acids was significantly altered. We suggest that the Y413 residue within a putative CRAC motif has a role in sterol-sensing and the ATPase/drug transport coupling in the ABCG2 multidrug transporter

    Unmatched Level of Molecular Convergence among Deeply Divergent Complex Multicellular Fungi

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    Convergent evolution is pervasive in nature, but it is poorly understood how various constraints and natural selection limit the diversity of evolvable phenotypes. Here, we analyze the transcriptome across fruiting body development to understand the independent evolution of complex multicellularity in the two largest clades of fungi-the Agarico- and Pezizomycotina. Despite >650 My of divergence between these clades, we find that very similar sets of genes have convergently been co-opted for complex multicellularity, followed by expansions of their gene families by duplications. Over 82% of shared multicellularity-related gene families were expanding in both clades, indicating a high prevalence of convergence also at the gene family level. This convergence is coupled with a rich inferred repertoire of multicellularityrelated genes in the most recent common ancestor of the Agarico- and Pezizomycotina, consistent with the hypothesis that the coding capacity of ancestral fungal genomes might have promoted the repeated evolution of complex multicellularity. We interpret this repertoire as an indication of evolutionary predisposition of fungal ancestors for evolving complex multicellular fruiting bodies. Our work suggests that evolutionary convergence may happen not only when organisms are closely related or are under similar selection pressures, but also when ancestral genomic repertoires render certain evolutionary trajectories more likely than others, even across large phylogenetic distances
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