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      Investigation of a Ni-Modified MCM-41 Catalyst for the Reduction of Oxygenates and Carbon Deposits during the Co-Pyrolysis of Cellulose and Polypropylene

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          Abstract

          Catalytic fast co-pyrolysis of biomass and plastic is an effective method to achieve high-quality bio-oil production. In this work, (Ni)-MCM-41 catalysts with different Ni loadings were prepared and characterized in detail by using a variety of advanced analytical techniques, and the effects on the catalytic performance were analyzed by micropyrolysis with gas chromatography mass spectrometry (Py-GC/MS) and thermogravimetry-Fourier transform infrared spectroscopy (TG-FTIR) methods. The results showed that an appropriate amount of Ni addition can effectively modulate the physicochemical properties of MCM-41. For a Ni loading of 25.1 wt % (Cat-C), the catalyst showed an optimal catalytic performance, a decrease in the proportion of oxygenated compounds in the product from 35.6 (MCM-41) to 13.4%, and an increase in the relative total amount of olefins plus aromatics from 62.2 (MCM-41) to 84.6%. The excellent catalytic performance of Cat-C can be ascribed to a balancing of its proper physical structural properties, appropriate acidity, strong metal–carrier interaction, high metal dispersion, and excellent compatibility balance between active and acidic sites.

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          Catalytic fast pyrolysis of lignocellulosic biomass.

          Increasing energy demand, especially in the transportation sector, and soaring CO2 emissions necessitate the exploitation of renewable sources of energy. Despite the large variety of new energy carriers, liquid hydrocarbon still appears to be the most attractive and feasible form of transportation fuel taking into account the energy density, stability and existing infrastructure. Biomass is an abundant, renewable source of energy; however, utilizing it in a cost-effective way is still a substantial challenge. Lignocellulose is composed of three major biopolymers, namely cellulose, hemicellulose and lignin. Fast pyrolysis of biomass is recognized as an efficient and feasible process to selectively convert lignocellulose into a liquid fuel-bio-oil. However bio-oil from fast pyrolysis contains a large amount of oxygen, distributed in hundreds of oxygenates. These oxygenates are the cause of many negative properties, such as low heating value, high corrosiveness, high viscosity, and instability; they also greatly limit the application of bio-oil particularly as transportation fuel. Hydrocarbons derived from biomass are most attractive because of their high energy density and compatibility with the existing infrastructure. Thus, converting lignocellulose into transportation fuels via catalytic fast pyrolysis has attracted much attention. Many studies related to catalytic fast pyrolysis of biomass have been published. The main challenge of this process is the development of active and stable catalysts that can deal with a large variety of decomposition intermediates from lignocellulose. This review starts with the current understanding of the chemistry in fast pyrolysis of lignocellulose and focuses on the development of catalysts in catalytic fast pyrolysis. Recent progress in the experimental studies on catalytic fast pyrolysis of biomass is also summarized with the emphasis on bio-oil yields and quality.
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            Catalytic co-pyrolysis of lignocellulosic biomass with polymers: a critical review

            A perspective and review of recent progress in the catalytic co-pyrolysis of lignocellulosic biomass with polymers is presented. The increasing demand for renewable chemicals and fuels requires the exploitation of alternative feedstock to replace petroleum-derived chemicals and fuels. Lignocellulosic biomass has been considered as the most promising feedstock for the production of sustainable biofuels. Catalytic fast pyrolysis (CFP) is more amenable to directly converting biomass into high quality biofuel. However, even in the presence of a highly efficient catalyst, the CFP of biomass can solely manufacture a low yield of aromatic hydrocarbon but a high formation of coke. The addition of a hydrogen-rich co-reactant ( e.g. waste plastics) in CFP can significantly improve the yield of aromatics and lower the coke formation. Catalytic co-pyrolysis can also reduce the disposal of waste polymers (plastics and waste tires) in landfills, solve some environmental issues, and further increase energy security. In this regard, this article reviews the catalytic co-pyrolysis process from several points of view, starting from feedstock characteristics and availability, current understanding of the chemistry in non-catalytic co-pyrolysis, and focusing on the chemistry in the catalytic co-pyrolysis of biomass with various categories of polymers. Recent progress in the experimental studies on both the non-catalytic pyrolysis and catalytic co-pyrolysis of biomass with polymers is also summarized with the emphasis on the liquid yield and quality. In addition, reaction kinetics and several outlooks in the light of current studies are also presented in the review. Consequently, this review demonstrates both highlights of the remarkable achievement of catalytic co-pyrolysis and the milestones that are necessary to be garnered in the future.
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              Catalytic conversion of biomass-derived feedstocks into olefins and aromatics with ZSM-5: the hydrogen to carbon effective ratio

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                05 August 2020
                18 August 2020
                : 5
                : 32
                : 20299-20310
                Affiliations
                []Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Energy and Power Engineering, Tsinghua University , Beijing 100084, China
                []Beijing Engineering Research Center for Ecological Restoration and Carbon Fixation of Saline−Alkaline and Desert Land, Tsinghua University , Beijing 100084, China
                [§ ]School of Electric Engineering, Xinjiang University , Urumqi 830047, China
                Author notes
                [* ]Email: zhuojk@ 123456mail.tsinghua.edu.cn . Tel: +86-10-62797509.
                Article
                10.1021/acsomega.0c02205
                7439362
                32832783
                e8a681a6-109a-4ba2-9515-65817f1757a5
                Copyright © 2020 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 12 May 2020
                : 22 June 2020
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