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description Publicationkeyboard_double_arrow_right Article , Journal 2019Publisher:MDPI AG Renfei Li; Wenbing Tan; Xinyu Zhao; Qiuling Dang; Qidao Song;Beidou Xi;
Xiaohui Zhang;Beidou Xi
Beidou Xi in OpenAIREdoi: 10.3390/catal9060539
Wood waste generated during the tree felling and processing is a rich, green, and renewable lignocellulosic biomass. However, an effective method to apply wood waste in anaerobic digestion is lacking. The high carbon to nitrogen (C/N) ratio and rich lignin content of wood waste are the major limiting factors for high biogas production. NaOH pre-treatment for lignocellulosic biomass is a promising approach to weaken the adverse effect of complex crystalline cellulosic structure on biogas production in anaerobic digestion, and the synergistic integration of lignocellulosic biomass with low C/N ratio biomass in anaerobic digestion is a logical option to balance the excessive C/N ratio. Here, we assessed the improvement of methane production of wood waste in anaerobic digestion by NaOH pretreatment, co-digestion technique, and their combination. The results showed that the methane yield of the single digestion of wood waste was increased by 38.5% after NaOH pretreatment compared with the untreated wood waste. The methane production of the co-digestion of wood waste and pig manure was higher than that of the single digestion of wood waste and had nonsignificant difference with the single-digestion of pig manure. The methane yield of the co-digestion of wood waste pretreated with NaOH and pig manure was increased by 75.8% than that of the untreated wood waste. The findings indicated that wood waste as a sustainable biomass source has considerable potential to achieve high biogas production in anaerobic digestion.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal9060539&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 21 citations 21 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal9060539&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2020Publisher:MDPI AG Using renewable energy to convert CO2 to a clean fuel ethanol can not only reduce carbon emission through the utilization of CO2 as feedstock, but also store renewable energy as the widely used chemical and high-energy-density fuel, being considered as a perfect strategy to address current environment and energy issues. Developing efficient electrocatalysts, photocatalysts, and photoelectrocatalysts for CO2 reduction is the most crucial keystone for achieving this goal. Considerable progresses in CO2-based ethanol production have been made over the past decades. This review provides the general principles and summarizes the latest advancements in electrocatalytic, photocatalytic and photoelectrocatalytic CO2 conversion to ethanol. Furthermore, the main challenges and proposed future prospects are illustrated for further developments in clean fuel ethanol production.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal10111287&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 30 citations 30 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal10111287&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2019 SpainPublisher:MDPI AG Authors: Vladimir Sánchez; Anton Dafinov; Pilar Salagre;Jordi Llorca;
+1 AuthorsJordi Llorca
Jordi Llorca in OpenAIREVladimir Sánchez; Anton Dafinov; Pilar Salagre;Jordi Llorca;
Jordi Llorca
Jordi Llorca in OpenAIREYolanda Cesteros;
Yolanda Cesteros
Yolanda Cesteros in OpenAIREdoi: 10.3390/catal9090706
handle: 2117/170994
It has previously been reported that the use of microwave heating, together with the presence of co-solvents, improves the efficiency of furfural production from biomass. Solid acid catalysts can be a good alternative to mineral acids, since they can prevent corrosion and can be reused. However, the formation of humines should be minimized. Several delaminated and fluorinated hectorites, with different types and strengths of acid sites, were synthesized and tested as catalysts for the production of furfural from commercial xylose and from an acid biomass extract of almond shells. A new methodology was developed to prepare crystalline fluorohectorite at 800 °C in just 3 h. The presence of F significantly increased the acidity strength in the protonated fluorohectorite (H-FH) taking into account its high ammonia desorption temperature (721 °C). Additionally, this sample had fourteen times higher total acidity by m2 than the reference H-βeta acid catalyst. H-FH was the most efficient catalyst at short reaction times (1 h) for the transformation of xylose to furfural under microwaves using toluene as co-solvent, regardless of whether the xylose was commercial (20% furfural yield) or an extract of almond shells (60% furfural yield). However, the acidity of the extract affected the fluorohectorite structure and composition.
Universitat Politècn... arrow_drop_down Universitat Politècnica de Catalunya, BarcelonaTech: UPCommons - Global access to UPC knowledgeArticle . 2019License: CC BY NC NDFull-Text: https://www.mdpi.com/2073-4344/9/9/706Data sources: Bielefeld Academic Search Engine (BASE)Recolector de Ciencia Abierta, RECOLECTAArticleData sources: Recolector de Ciencia Abierta, RECOLECTARecolector de Ciencia Abierta, RECOLECTAArticle . 2019License: CC BY NC NDData sources: Recolector de Ciencia Abierta, RECOLECTAadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal9090706&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 5 citations 5 popularity Top 10% influence Average impulse Average Powered by BIP!
visibility 176visibility views 176 download downloads 1,801 Powered bymore_vert Universitat Politècn... arrow_drop_down Universitat Politècnica de Catalunya, BarcelonaTech: UPCommons - Global access to UPC knowledgeArticle . 2019License: CC BY NC NDFull-Text: https://www.mdpi.com/2073-4344/9/9/706Data sources: Bielefeld Academic Search Engine (BASE)Recolector de Ciencia Abierta, RECOLECTAArticleData sources: Recolector de Ciencia Abierta, RECOLECTARecolector de Ciencia Abierta, RECOLECTAArticle . 2019License: CC BY NC NDData sources: Recolector de Ciencia Abierta, RECOLECTAadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal9090706&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2021Publisher:MDPI AG Authors: Xinsheng Li;Jifeng Pang;
Jingcai Zhang; Xianquan Li; +4 AuthorsJifeng Pang
Jifeng Pang in OpenAIREXinsheng Li;Jifeng Pang;
Jingcai Zhang; Xianquan Li; Yu Jiang; Yang Su; Weizhen Li;Jifeng Pang
Jifeng Pang in OpenAIREMingyuan Zheng;
Mingyuan Zheng
Mingyuan Zheng in OpenAIRECatalytic conversion of biomass-derived feedstock to high-value chemicals is of remarkable significance for alleviating dependence on fossil energy resources. MgAl spinel-supported Pt catalysts were prepared and used in furfuryl alcohol conversion. The approaches to tune the reaction selectivity toward pentanediols (PeDs) were investigated and the catalytic performance was correlated to the catalysts’ physicochemical properties based on comprehensive characterizations. It was found that 1–8 wt% Pt was highly dispersed on the MgAl2O4 support as nanoparticles with small sizes of 1–3 nm. The reaction selectivity did not show dependence on the size of Pt nanoparticles. Introducing LiOH onto the support effectively steered the reaction products toward the PeDs at the expense of tetrahydrofurfuryl alcohol (THFA) selectivity. Meanwhile, the major product in PeDs was shifted from 1,5-PeD to 1,2-PeD. The reasons for the PeDs selectivity enhancement were attributed to the generation of a large number of medium-strong base sites on the Li-modified Pt catalyst. The reaction temperature is another effective factor to tune the reaction selectivity. At 230 °C, PeDs selectivity was enhanced to 77.4% with a 1,2-PeD to 1,5-PeD ratio of 3.7 over 4Pt/10Li/MgAl2O4. The Pt/Li/MgAl2O4 catalyst was robust to be reused five times without deactivation.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal11040415&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 5 citations 5 popularity Average influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal11040415&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2019 ItalyPublisher:MDPI AG Authors:Carlucci, Claudia;
Carlucci, Claudia
Carlucci, Claudia in OpenAIREDegennaro, Leonardo;
Degennaro, Leonardo
Degennaro, Leonardo in OpenAIRELuisi, Renzo;
Luisi, Renzo
Luisi, Renzo in OpenAIREdoi: 10.3390/catal9010075
handle: 11586/225889
The discovery of alternative fuels that can replace conventional fuels has become the goal of many scientific researches. Biodiesel is produced from vegetable oils through a transesterification reaction that converts triglycerides into fatty acid methyl esters (FAME), with the use of a low molecular weight alcohol, in different reaction conditions and with different types of catalysts. Titanium dioxide has shown a high potential as heterogeneous catalyst due to high surface area, strong metal support interaction, chemical stability, and acid–base property. This review focused on TiO2 as heterogeneous catalyst and its potential applications in the continuous flow production of biodiesel. Furthermore, the use of micro reactors, able to make possible chemical transformations not feasible with traditional techniques, will enable a reduction of production costs and a greater environmental protection.
Università degli Stu... arrow_drop_down Università degli Studi di Bari Aldo Moro: CINECA IRISArticle . 2019Full-Text: http://hdl.handle.net/11586/225889Data sources: Bielefeld Academic Search Engine (BASE)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal9010075&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 77 citations 77 popularity Top 1% influence Top 10% impulse Top 1% Powered by BIP!
more_vert Università degli Stu... arrow_drop_down Università degli Studi di Bari Aldo Moro: CINECA IRISArticle . 2019Full-Text: http://hdl.handle.net/11586/225889Data sources: Bielefeld Academic Search Engine (BASE)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal9010075&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2021Publisher:MDPI AG Authors: Alexey A. Petrov;Daniil A. Lukyanov;
Oleg A. Kopytko;Daniil A. Lukyanov
Daniil A. Lukyanov in OpenAIREJulia V. Novoselova;
+2 AuthorsJulia V. Novoselova
Julia V. Novoselova in OpenAIREAlexey A. Petrov;Daniil A. Lukyanov;
Oleg A. Kopytko;Daniil A. Lukyanov
Daniil A. Lukyanov in OpenAIREJulia V. Novoselova;
Julia V. Novoselova
Julia V. Novoselova in OpenAIREElena V. Alekseeva;
Elena V. Alekseeva
Elena V. Alekseeva in OpenAIREOleg V. Levin;
Oleg V. Levin
Oleg V. Levin in OpenAIREConductive polymers are widely used as active and auxiliary materials for organic photovoltaic cells due to their easily tunable properties, high electronic conductivity, and light absorption. Several conductive polymers show the cathodic photogalvanic effect in pristine state. Recently, photoelectrochemical oxygen reduction has been demonstrated for nickel complexes of Salen-type ligands. Herein, we report an unexpected inversion of the photogalvanic effect caused by doping of the NiSalen polymers with anionic porphyrins. The observed effect was studied by means of UV-Vis spectroscopy, cyclic voltammetry and chopped light chronoamperometry. While pristine NiSalens exhibit cathodic photopolarization, doping with porphyrins inverts the polarization. As a result, photoelectrochemical oxidation of the ascorbate proceeds smoothly on the NiSalen electrode doped with zinc porphyrins. The highest photocurrents were observed on NiSalen polymer with o-phenylene imine bridge, doped with anionic zinc porphyrin. Assuming this, porphyrin serves both as a catalytic center for the oxidation of ascorbate and an internal electron donor, facilitating the photoinduced charge transport and anodic depolarization.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal11060729&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 7 citations 7 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal11060729&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2013 SpainPublisher:MDPI AG Authors: Martínez Huerta, M. Victoria; Tsiouvaras, Nikolaos;García, Gonzalo;
García, Gonzalo
García, Gonzalo in OpenAIREPeña Jiménez, Miguel Antonio;
+3 AuthorsPeña Jiménez, Miguel Antonio
Peña Jiménez, Miguel Antonio in OpenAIREMartínez Huerta, M. Victoria; Tsiouvaras, Nikolaos;García, Gonzalo;
García, Gonzalo
García, Gonzalo in OpenAIREPeña Jiménez, Miguel Antonio;
Peña Jiménez, Miguel Antonio
Peña Jiménez, Miguel Antonio in OpenAIREPastor Tejera, Elena;
Rodriguez, José L.; García Fierro, José Luis;Pastor Tejera, Elena
Pastor Tejera, Elena in OpenAIREdoi: 10.3390/catal3040811
handle: 10261/157717
The review article discusses the current status and recent findings of our investigations on the synthesis and characterization of carbon-supported PtRuMo electrocatalysts for direct alcohol fuel cells. In particular, the effect of the carbon support and the composition on the structure, stability and the activity of the PtRuMo nanoparticles for the electrooxidation of CO, methanol and ethanol have been studied. Different physicochemical techniques have been employed for the analysis of the catalysts structures: X-ray analytical methods (XRD, XPS, TXRF), thermogravimetry (TGA) and transmission electron microscopy (TEM), as well as a number of electrochemical techniques like CO adsorption studies, current-time curves and cyclic voltammetry measurements. Furthermore, spectroscopic methods adapted to the electrochemical systems for in situ studies, such as Fourier transform infrared spectroscopy (FTIRS) and differential electrochemical mass spectrometry (DEMS), have been used to evaluate the oxidation process of CO, methanol and ethanol over the carbon-supported PtRuMo electrocatalysts.
Catalysts arrow_drop_down Recolector de Ciencia Abierta, RECOLECTAArticle . 2013 . Peer-reviewedData sources: Recolector de Ciencia Abierta, RECOLECTAadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal3040811&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 13 citations 13 popularity Average influence Average impulse Average Powered by BIP!
visibility 10visibility views 10 download downloads 56 Powered bymore_vert Catalysts arrow_drop_down Recolector de Ciencia Abierta, RECOLECTAArticle . 2013 . Peer-reviewedData sources: Recolector de Ciencia Abierta, RECOLECTAadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal3040811&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2023Publisher:MDPI AG Authors: Maryam Hanif; Ijaz Ahmad Bhatti;Muhammad Asif Hanif;
Muhammad Asif Hanif
Muhammad Asif Hanif in OpenAIREUmer Rashid;
+3 AuthorsUmer Rashid
Umer Rashid in OpenAIREMaryam Hanif; Ijaz Ahmad Bhatti;Muhammad Asif Hanif;
Muhammad Asif Hanif
Muhammad Asif Hanif in OpenAIREUmer Rashid;
Bryan R. Moser; Asma Hanif; Fahad A. Alharthi;Umer Rashid
Umer Rashid in OpenAIREProduction of biodiesel from edible vegetable oils using homogenous catalysts negatively impacts food availability and cost while generating significant amounts of caustic wastewater during purification. Thus, there is an urgent need to utilize low-cost, non-food feedstocks for the production of biodiesel using sustainable heterogeneous catalysis. The objective of this study was to synthesize a novel supported nano-magnetic catalyst (CaO/Fe2O3/feldspar) for the production of biodiesel (fatty acid methyl esters) from waste and low-cost plant seed oils, including Sinapis arvensis (wild mustard), Carthamus oxyacantha (wild safflower) and Pongamia pinnata (karanja). The structure, morphology, surface area, porosity, crystallinity, and magnetization of the nano-magnetic catalyst was confirmed using XRD, FESEM/EDX, BET, and VSM. The maximum biodiesel yield (93.6–99.9%) was achieved at 1.0 or 1.5 wt.% catalyst with methanol-to-oil molar ratios of 5:1 or 10:1 at 40 °C for 2 h. The CaO/Fe2O3/feldspar catalyst retained high activity for four consecutive cycles for conversion of karanja, wild mustard, and wild safflower oils. The effective separation of the catalyst from biodiesel was achieved using an external magnet. Various different physico-chemical parameters, such as pour point, density, cloud point, iodine value, acid value, and cetane number, were also determined for the optimized fuels and found to be within the ranges specified in ASTM D6751 and EN 14214, where applicable.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13060998&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 3 citations 3 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13060998&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2021 United KingdomPublisher:MDPI AG Authors:Ishaka Muhammad;
Ishaka Muhammad
Ishaka Muhammad in OpenAIREGeorge Manos;
George Manos
George Manos in OpenAIREBiomass pyrolysis is a promising technology for fuel and chemical production from an abundant renewable source. It takes place usually in two stages; non-catalytic pyrolysis with further catalytic upgrading of the formed pyrolysis oil. The direct catalytic pyrolysis of biomass reduces the pyrolysis temperature, increase the yield to target products and improves their quality. However, in such one-stage process the contact between biomass and solid catalyst particles is poor leading to an excessively high degree of pure thermal pyrolysis reactions. The aim of this study was to enhance the catalyst-biomass contact via co-pressing of biomass and catalyst particles as a pre-treatment method. Catalytic pyrolysis of biomass components with HY and USY zeolites was studied using thermogravimetric analysis (TGA), as well as experiments in a pyrolysis reactor. The liquid and coke yields were characterized using gas chromatography, and TGA respectively. The TGA results showed that the degradation of the co-pressed cellulose occurred at lower temperatures compared to the pure thermal degradation, as well as catalytic degradation of non-pretreated cellulose. All biomass components produced better results using the co-pressing method, where the liquid yields increased while coke/char yields decreased. Bio-oil from catalytic pyrolysis of cellulose with HY catalyst mainly produced heavier fractions, while in the presence of USY catalyst medium fraction was mainly produced within the gasoline range. For hemicellulose catalytic pyrolysis, the catalysts had similar effects in enhancing the lighter fraction, but specifically, HY showed higher selectivity to middle fraction while USY has produced higher percentage of lighter fraction. Using with both catalysts, co-pressing had the best effect of eliminating the heavier fraction and improving the gasoline range fraction. Spent catalyst from co-pressed sample had lower concentrations of coke/char components due to the shorter residence times of volatiles, which suppresses the occurrence of secondary reactions leading to coke/char formations.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal11070805&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 14 citations 14 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2023Publisher:MDPI AG Authors:K. A. Viraj Miyuranga;
K. A. Viraj Miyuranga
K. A. Viraj Miyuranga in OpenAIREUdara S. P. R. Arachchige;
T. M. M. Marso;Udara S. P. R. Arachchige
Udara S. P. R. Arachchige in OpenAIREGamunu Samarakoon;
Gamunu Samarakoon
Gamunu Samarakoon in OpenAIREFor the production of biodiesel from waste cooking oil with an acid value of 1.86 mg KOH/g, five heterogeneous catalysts—Ba(OH)2, CaO, MgO, ZnO, and AlCl3—were employed. To optimize the reaction parameters of each catalyst, the influence of crucial process variables, such as catalyst loading, methanol-to-oil ratio, and reaction duration, was investigated. In addition, the effect of acetone as a cosolvent toward the progress of biodiesel production and the reusability of the heterogeneous catalysts were also examined, and the data were statistically evaluated with a 95% confidence level. Ba(OH)2 performed exceptionally well, with a 92 wt.% biodiesel yield, followed by CaO with an 84 wt.% yield. However, none of the results for MgO, ZnO, or AlCl3 were adequate. In addition, regardless of the type of catalyst utilized, adding 20 vol.% acetone to the biodiesel manufacturing process led to an increase in output. Furthermore, every heterogeneous catalyst was reusable, but only Ba(OH)2 and CaO produced a significant yield until the third cycle. The other catalysts did not produce yields of any significance.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euAccess Routesgold 15 citations 15 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13030546&type=result"></script>'); --> </script>
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