“…Wood, such as Ulin wood residue, is well pyrolyzed due to the high content of hydrocarbon and the small content of moisture. Moreover, biochar, as a side-product of pyrolysis, also can be transformed to be a more valuable product, such as biobriquette [14] and catalyst support [15] since pyrolysis has received many interests for the bioenergy production from biomass so that the kinetic study of pyrolysis is useful to be investigated.…”
Biomass as a renewable and sustainable energy source is expected to solve the energy crisis problem. Ulin wood residues as a biomass source could be converted into bioenergy utilizing the pyrolysis process since its primary component is a hydrocarbon. Pyrolysis process has received many interests for bioenergy production from biomass, elevating the importance of the kinetic study of pyrolysis. The kinetic study of pyrolysis is related to the beginning stage behavior of gasification and combustion process. The kinetic mechanism of pyrolysis is analyzed using Thermogravimetry Analysis (TGA), by estimating the mass decomposition at solid-state that shows TG and DTG curve. The TG and DTG curves were analyzed to see the effect of heating rate on decomposition temperature. This experiment was performed by heating 10 mg of Ulin wood sawdust from ambient temperature to 1473 K utilizing 100 mL/min of nitrogen (N 2) gas as carrier gas at various heating rate: 5, 10, 20, and 50 K/min. The kinetic parameters were determined by applying the iso-conversional methods, the Kissinger-Akahira-Sunose (KAS) and Flynn-Wall-Ozawa (FWO) methods, and then compared the results with the non iso-conversional method, using Kissinger method. The average value of activation energy calculated using the KAS and FWO methods are 253.5514 and 245.2512 kJ/mol, with the average value of constant coefficient square (R 2) of 0.9848 and 0.9859, respectively, whereas the calculated activation energy and R 2 using the Kissinger method are 237.4478 kJ/mol and 0.8520, respectively.
“…Wood, such as Ulin wood residue, is well pyrolyzed due to the high content of hydrocarbon and the small content of moisture. Moreover, biochar, as a side-product of pyrolysis, also can be transformed to be a more valuable product, such as biobriquette [14] and catalyst support [15] since pyrolysis has received many interests for the bioenergy production from biomass so that the kinetic study of pyrolysis is useful to be investigated.…”
Biomass as a renewable and sustainable energy source is expected to solve the energy crisis problem. Ulin wood residues as a biomass source could be converted into bioenergy utilizing the pyrolysis process since its primary component is a hydrocarbon. Pyrolysis process has received many interests for bioenergy production from biomass, elevating the importance of the kinetic study of pyrolysis. The kinetic study of pyrolysis is related to the beginning stage behavior of gasification and combustion process. The kinetic mechanism of pyrolysis is analyzed using Thermogravimetry Analysis (TGA), by estimating the mass decomposition at solid-state that shows TG and DTG curve. The TG and DTG curves were analyzed to see the effect of heating rate on decomposition temperature. This experiment was performed by heating 10 mg of Ulin wood sawdust from ambient temperature to 1473 K utilizing 100 mL/min of nitrogen (N 2) gas as carrier gas at various heating rate: 5, 10, 20, and 50 K/min. The kinetic parameters were determined by applying the iso-conversional methods, the Kissinger-Akahira-Sunose (KAS) and Flynn-Wall-Ozawa (FWO) methods, and then compared the results with the non iso-conversional method, using Kissinger method. The average value of activation energy calculated using the KAS and FWO methods are 253.5514 and 245.2512 kJ/mol, with the average value of constant coefficient square (R 2) of 0.9848 and 0.9859, respectively, whereas the calculated activation energy and R 2 using the Kissinger method are 237.4478 kJ/mol and 0.8520, respectively.
“…Various carbon materials including carbon nanofibers [ 34 ], carbon nanotubes [ 35 , 36 , 37 , 38 ], biochar [ 39 ], and carbon felt [ 40 ] have also been employed as carriers for CO 2 hydrogenation catalysts, taking advantage of their high hydrogen storage capacity, high thermal conductivity, and high specific surface area of carbon carriers. Nanosized materials are used to define nanoscale catalyst structures, in which the composition of catalysts and their surface structures can be adjusted and may bring to darewidespread applications.…”
Rapid growth in the world’s economy depends on a significant increase in energy consumption. As is known, most of the present energy supply comes from coal, oil, and natural gas. The overreliance on fossil energy brings serious environmental problems in addition to the scarcity of energy. One of the most concerning environmental problems is the large contribution to global warming because of the massive discharge of CO2 in the burning of fossil fuels. Therefore, many efforts have been made to resolve such issues. Among them, the preparation of valuable fuels or chemicals from greenhouse gas (CO2) has attracted great attention because it has made a promising step toward simultaneously resolving the environment and energy problems. This article reviews the current progress in CO2 conversion via different strategies, including thermal catalysis, electrocatalysis, photocatalysis, and photoelectrocatalysis. Inspired by natural photosynthesis, light-capturing agents including macrocycles with conjugated structures similar to chlorophyll have attracted increasing attention. Using such macrocycles as photosensitizers, photocatalysis, photoelectrocatalysis, or coupling with enzymatic reactions were conducted to fulfill the conversion of CO2 with high efficiency and specificity. Recent progress in enzyme coupled to photocatalysis and enzyme coupled to photoelectrocatalysis were specially reviewed in this review. Additionally, the characteristics, advantages, and disadvantages of different conversion methods were also presented. We wish to provide certain constructive ideas for new investigators and deep insights into the research of CO2 conversion.
“…Many different types of supporting materials have been reported for methanation catalyst, including Al 2 O 3 , SiO 2 , ZrO 2 , TiO 2 , and CeO 2 ; as well as structured metal oxides, carbon, and zeolite materials [ 78 , 80 , 85 ]. Among the carbon materials that have been employed as a support for methanation catalysts, we found carbon nanotubes [ 86 , 87 ], activated carbon [ 88 ], carbon nanofiber [ 89 ], biochar-based materials [ 90 , 91 , 92 ], and carbon felt [ 93 ]. As an example, carbon nanotubes have been widely used as a support of metal nanoparticles due to their exceptional physico-chemical properties.…”
Section: Biochar-based Materials For Catalysismentioning
confidence: 99%
“…For CO 2 methanation, an N-doped biochar from Pynus sylvestris was obtained by pyrolysis and activation using urea as the nitrogen precursor and NaHCO 3 as the activating agent [ 92 ]. Biochar obtained in this way was modified with Ru nanoparticles by the wet impregnation method.…”
Section: Biochar-based Materials For Catalysismentioning
confidence: 99%
“…Temperature dependence of CO 2 methanation over the catalysts: ( C ) the CO 2 conversion; ( D ) the CH 4 and CO selectivity. Reproduced from [ 92 ] with permission from Elsevier 2020.…”
Sustainable activated carbon can be obtained from the pyrolysis/activation of biomass wastes coming from different origins. Carbon obtained in this way shows interesting properties, such as high surface area, electrical conductivity, thermal and chemical stability, and porosity. These characteristics among others, such as a tailored pore size distribution and the possibility of functionalization, lead to an increased use of activated carbons in catalysis. The use of activated carbons from biomass origins is a step forward in the development of more sustainable processes enhancing material recycling and reuse in the frame of a circular economy. In this article, a perspective of different heterogeneous catalysts based on sustainable activated carbon from biomass origins will be analyzed focusing on their properties and catalytic performance for determined energy-related applications. In this way, the article aims to give the reader a scope of the potential of these tailor-made sustainable materials as a support in heterogeneous catalysis and future developments needed to improve catalyst performance. The selected applications are those related with H2 energy and the production of biomethane for energy through CO2 methanation.
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