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description Publicationkeyboard_double_arrow_right Article , Journal 2021Publisher:Elsevier BV Authors:Shu Zhang;
Shu Zhang
Shu Zhang in OpenAIREJun Xiang;
Haisheng Lin; Yi Wang; +5 AuthorsJun Xiang
Jun Xiang in OpenAIREShu Zhang;
Shu Zhang
Shu Zhang in OpenAIREJun Xiang;
Haisheng Lin; Yi Wang; Xun Hu; Qingyin Li; Mortaza Gholizadeh; Song Hu; Xiangzhou Yuan;Jun Xiang
Jun Xiang in OpenAIREpmid: 34118669
Co-hydrothermal carbonization (HTC) of livestock manure and biomass might improve the fuel properties of the hydrochar due to the high reactivity of the biomass-derived intermediates with the abundant oxygen-containing functionalities. However, the complicated compositions make it difficult to explicit the specific roles of the individual components of biomass played in the co-HTC process. In this study, cellulose was used for co-HTC with swine manure to investigate the influence on the properties of the hydrochar. The yield of hydrochar obtained from co-HTC reduced gradually with the cellulose proportion increased, and the solid yield was lower than the theoretical value. This was because the cellulose-derived intermediates favored the stability of the fragments from hydrolysis of swine manure. The increased temperature resulted in the reduction of the hydrochar yield whereas the prolonged time enhanced the formation of solid product. The interaction of the co-HTC intermediates facilitated the formation of O-containing species, thus making the solid more oxygen- and hydrogen-rich with a higher volatility. In addition, the co-HTC affected the evolution of functionalities like -OH and CO during the thermal treatment of the hydrochar and altered its morphology by stuffing the pores from swine manure-derived solid with the microspheres from HTC of cellulose. The interaction of the varied intermediates also impacted the formation of amines, ketones, carboxylic acids, esters, aromatics and the polymeric products in distinct ways.
The Science of The T... arrow_drop_down The Science of The Total EnvironmentArticle . 2021 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd 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=10.1016/j.scitotenv.2021.148134&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 25 citations 25 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert The Science of The T... arrow_drop_down The Science of The Total EnvironmentArticle . 2021 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd 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=10.1016/j.scitotenv.2021.148134&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2016Publisher:Elsevier BV Authors:Jun Xiang;
Jun Xiang
Jun Xiang in OpenAIREChuan Ma;
Chuan Ma
Chuan Ma in OpenAIREBen Wang;
Ben Wang
Ben Wang in OpenAIREJie Yu;
+4 AuthorsJun Xiang;
Jun Xiang
Jun Xiang in OpenAIREChuan Ma;
Chuan Ma
Chuan Ma in OpenAIREBen Wang;
Ben Wang
Ben Wang in OpenAIREJie Yu;
Zijian Song; Lushi Sun; Song Hu; Sheng Su;Abstract Electronic waste plastics (e-waste plastics) have been one of the emerging and fastest-growing waste streams due to the increasing number of generation in waste electrical and electronic equipment (WEEE). Given that brominated flame retardant (BFR) materials in e-waste plastics have been the major impediment for recycling treatment, chemical recycling has been proposed as an environmentally friendly method of recycling e-waste plastics for clean fuels production or chemical feedstocks. This paper summarized the current techniques of BFR-plastics recycling with a view to solving energy crisis and the environmental degradation of BFR-plastics. Emphasis was paid on the recent chemical treatment of BFR-plastics, including pyrolysis, co-pyrolysis and catalytic cracking, which are yet to be completely feasible in conversion of BFR-plastics for clean fuels production. Hydrothermal treatment is regarded as a novel high-efficiency technology to recycle BFR-plastics, which can be a potential process for the in situ debromination of oil products. An advanced chemical recycling technique, pyrolysis-catalytic upgrading process, is highlighted. The recycling route of pyrolyzing BFR-plastics prior to catalytic upgrading was intended to obtain high quantity oils, and then the upgrading process of pyrolysis oils was conducted by means of catalytic hydrodebromination with the aim of obtaining bromine-free oils for commercial applications. In short, the integration of pyrolysis with catalytic upgrading process can provide significant economic and environmental options in conversion of e-waste plastics into useful and high-value materials. Further investigations are required to develop the pyrolysis-catalytic upgrading process to become sustainable and commercially viable for clean fuels production.
Renewable and Sustai... arrow_drop_down Renewable and Sustainable Energy ReviewsArticle . 2016 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd 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=10.1016/j.rser.2016.04.020&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 228 citations 228 popularity Top 1% influence Top 10% impulse Top 1% Powered by BIP!
more_vert Renewable and Sustai... arrow_drop_down Renewable and Sustainable Energy ReviewsArticle . 2016 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd 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=10.1016/j.rser.2016.04.020&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2021Publisher:Elsevier BV Authors:Abdulmajid Abdullahi Shagali;
Song Hu; Yankui Wang;Abdulmajid Abdullahi Shagali
Abdulmajid Abdullahi Shagali in OpenAIREHanjian Li;
+3 AuthorsHanjian Li
Hanjian Li in OpenAIREAbdulmajid Abdullahi Shagali;
Song Hu; Yankui Wang;Abdulmajid Abdullahi Shagali
Abdulmajid Abdullahi Shagali in OpenAIREHanjian Li;
Yi Wang; Sheng Su;Hanjian Li
Hanjian Li in OpenAIREJun Xiang;
Jun Xiang
Jun Xiang in OpenAIREPyrolysis of walnut shells to biochar at 700 °C using N2gas was compared to one-step activation using steam/KOH under four different heating rates (10–40 °C/min). Steam biochars developed better surface area property of 342–556 m2/g compared to others (19–135 m2/g) over the same heating rates; meanwhile, increasing heating rate caused functional groups alteration and was distinct on the surface area property as about six-fold and two-fold difference from the lower to higher rates were recorded in neutral char and the steam/KOH activated biochars respectively. Increasing heating rate affected the neutral and steam biochars’ Raman intensity ratio whereas trivial influence was recorded on KOH-biochars.
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=10.1016/j.egyr.2021.10.021&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 17 citations 17 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=10.1016/j.egyr.2021.10.021&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2019Publisher:Elsevier BV Authors:Yuewen Shao;
Yuewen Shao
Yuewen Shao in OpenAIREXun Hu;
Zhanming Zhang; Kai Sun; +6 AuthorsYuewen Shao;
Yuewen Shao
Yuewen Shao in OpenAIREXun Hu;
Zhanming Zhang; Kai Sun; Guanggang Gao; Tao Wei;Shu Zhang;
Shu Zhang
Shu Zhang in OpenAIRESong Hu;
Song Hu
Song Hu in OpenAIREJun Xiang;
Jun Xiang
Jun Xiang in OpenAIREYi Wang;
This study investigated the conversion of furfural to 5-hydroxymethylfurfural (HMF) and further to levulinic acid/ester in dimethoxymethane under acidic conditions, with the particular focus on understanding the mechanism for polymer formation. The results showed that furfural could react with dimethoxymethane via electrophilic substitution reaction to form HMF or the ether/acetal of HMF, which were further converted to levulinic acid and methyl levulinate. The polymerization of furfural and the cross-polymerization between dimethoxymethane and the levulinic acid/ester produced were the main side reactions leading to the decreased yields of levulinic acid/ester. Comparing to the other solvent, methanol as the co-solvent helped to alleviate but not totally inhibited the occurrences of the polymerization, as the polymerization reactions via aldol condensation did not eliminate the CO functionalities. As a consequence, the polymerization reactions continued to proceed. Other co-solvent used such as guaiacol, dimethyl sulfoxide and acetone interfered with the transformation of furfural to HMF or aided the polymerization reactions. The polymer produced from the reactions between furfural and DMM was different from that produced from levulinic acid/ester. The former had a higher crystallinity, while the latter was more aliphatic. The DRIFTS and TG-MS studies showed that the polymer had the carboxylic group, methyl group and the aliphatic structure in the skeleton. The removal of these functionalities was accompanied by the aromatization of the polymer. The condensation of DMM with levulinic acid/ester was the key reason for the diminished production of levulinic acid/ester. Keywords: Furfural, Dimethoxymethane, Levulinic acid/ester, Mechanism for polymerization, Properties of the polymer
Green Energy & E... arrow_drop_down Green Energy & EnvironmentArticle . 2019 . Peer-reviewedLicense: CC BY NC NDData sources: Crossrefadd 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=10.1016/j.gee.2018.10.002&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 82 citations 82 popularity Top 1% influence Top 10% impulse Top 1% Powered by BIP!
more_vert Green Energy & E... arrow_drop_down Green Energy & EnvironmentArticle . 2019 . Peer-reviewedLicense: CC BY NC NDData sources: Crossrefadd 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=10.1016/j.gee.2018.10.002&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2022Publisher:Elsevier BV Authors: Aishu Li;Hengda Han;
Song Hu;Hengda Han
Hengda Han in OpenAIREMeng Zhu;
+6 AuthorsMeng Zhu
Meng Zhu in OpenAIREAishu Li;Hengda Han;
Song Hu;Hengda Han
Hengda Han in OpenAIREMeng Zhu;
Meng Zhu
Meng Zhu in OpenAIREQiangqiang Ren;
Yi Wang; Jun Xu; Long Jiang; Sheng Su;Qiangqiang Ren
Qiangqiang Ren in OpenAIREJun Xiang;
Jun Xiang
Jun Xiang in OpenAIREEnergy Conversion an... arrow_drop_down Energy Conversion and ManagementArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd 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=10.1016/j.enconman.2022.115205&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu30 citations 30 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert Energy Conversion an... arrow_drop_down Energy Conversion and ManagementArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd 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=10.1016/j.enconman.2022.115205&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2014Publisher:Elsevier BV Authors: Lushi Sun; Pengying Wang;Jun Xiang;
Huawei You; +4 AuthorsJun Xiang
Jun Xiang in OpenAIRELushi Sun; Pengying Wang;Jun Xiang;
Huawei You; Sheng Su; Song Hu; Yun Zhang; Fan Cao;Jun Xiang
Jun Xiang in OpenAIREpmid: 24332734
MnOx-CeO2/γ-Al2O3 (MnCe) selective catalytic reduction (SCR) catalysts prepared by sol-gel method were employed for low-temperature Hg(0) oxidation on a fixed-bed experimental setup. BET, XRD and XPS were used to characterize the catalysts. MnCe catalysts exhibited high Hg(0) oxidation activity at low temperatures (100-250 °C) under the simulated flue gas (O2, CO2, NO, SO2, HCl, H2O and balanced with N2). Only a small decrease in mercury oxidation was observed in the presence of 1200 ppm SO2, which proved that the addition of Ce helped resist SO2 poisoning. An enhancing effect of NO was observed due to the formation of multi-activity NOx species. The presence of HCl alone had excellent Hg(0) oxidation ability, while 10 ppm HCl plus 5% O2 further increased Hg(0) oxidation efficiency to 100%. Hg(0) oxidation on the MnCe catalyst surface followed the Langmiur-Hinshelwood mechanism, where reactions took place between the adsorbed active species and adsorbed Hg(0) to form Hg(2+). NH3 competed with Hg(0) for active sites on the catalyst surface, hence inhibiting Hg(0) oxidation. This study shows the feasibility of a single-step process integrating low-temperature SCR and Hg(0) oxidation from the coal combustion flue gas.
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=10.1016/j.chemosphere.2013.11.034&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 84 citations 84 popularity Top 10% influence Top 10% 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=10.1016/j.chemosphere.2013.11.034&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu