Efficient Oxidative Depolymerization of Xilinguole Lignite to Produce Humic Acids with Little CO2 Production

At present, non-fuel utilization as alternative chemical feedstocks becomes very important and significant for the efficient conversion of lignite. To reduce CO 2 production, an oxy-cracking technique in weak alkaline aqueous was conducted to selectively depolymerize Xilinguole lignite (XL) into hum...

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Veröffentlicht in:Solid fuel chemistry 2021-09, Vol.55 (5), p.348-356
Hauptverfasser: Wang, Z. C., Wu, Z. Q., Wang, Q., Pan, C. X., Yan, J. C., Li, Z. K., Lei, Z. P., Ren, S. B., Wang, X. L., Kang, S. G., Shui, H. F.
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container_end_page 356
container_issue 5
container_start_page 348
container_title Solid fuel chemistry
container_volume 55
creator Wang, Z. C.
Wu, Z. Q.
Wang, Q.
Pan, C. X.
Yan, J. C.
Li, Z. K.
Lei, Z. P.
Ren, S. B.
Wang, X. L.
Kang, S. G.
Shui, H. F.
description At present, non-fuel utilization as alternative chemical feedstocks becomes very important and significant for the efficient conversion of lignite. To reduce CO 2 production, an oxy-cracking technique in weak alkaline aqueous was conducted to selectively depolymerize Xilinguole lignite (XL) into humic acid (HA) under mild condition in this paper. The results indicated that XL has high reactivity, and can be depolymerized into HA with very little CO 2 . Elevated temperature is favorable for cracking of XL and converting HA into small molecular water-soluble acids and CO 2 . KOH mainly catalyzes the oxidative depolymerization of XL macromolecular structure. Lower temperature can reduce the formation of CO 2 and the usage of alkali. Under 80°C, KOH/XL = 0.33 and 2 h, HA weight yield was the highest, reaching 81%, as well as no CO 2 detected. Further, the obtained HA was separated and characterized by FTIR, CPMAS 13 C-NMR, TG/DTG and element analyses. Compared to XL and oxidized residue, HA contains more OH and COOH groups and aromatic rings, and less aliphatic groups. Due to low alkali usage and negligible CO 2 , the oxidative depolymerization of XL to produce HA shows high utilization efficiency of carbon, and is a promising clean and efficient utilization approach.
doi_str_mv 10.3103/S0361521921050086
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C. ; Wu, Z. Q. ; Wang, Q. ; Pan, C. X. ; Yan, J. C. ; Li, Z. K. ; Lei, Z. P. ; Ren, S. B. ; Wang, X. L. ; Kang, S. G. ; Shui, H. F.</creator><creatorcontrib>Wang, Z. C. ; Wu, Z. Q. ; Wang, Q. ; Pan, C. X. ; Yan, J. C. ; Li, Z. K. ; Lei, Z. P. ; Ren, S. B. ; Wang, X. L. ; Kang, S. G. ; Shui, H. F.</creatorcontrib><description>At present, non-fuel utilization as alternative chemical feedstocks becomes very important and significant for the efficient conversion of lignite. To reduce CO 2 production, an oxy-cracking technique in weak alkaline aqueous was conducted to selectively depolymerize Xilinguole lignite (XL) into humic acid (HA) under mild condition in this paper. The results indicated that XL has high reactivity, and can be depolymerized into HA with very little CO 2 . Elevated temperature is favorable for cracking of XL and converting HA into small molecular water-soluble acids and CO 2 . KOH mainly catalyzes the oxidative depolymerization of XL macromolecular structure. Lower temperature can reduce the formation of CO 2 and the usage of alkali. Under 80°C, KOH/XL = 0.33 and 2 h, HA weight yield was the highest, reaching 81%, as well as no CO 2 detected. Further, the obtained HA was separated and characterized by FTIR, CPMAS 13 C-NMR, TG/DTG and element analyses. Compared to XL and oxidized residue, HA contains more OH and COOH groups and aromatic rings, and less aliphatic groups. Due to low alkali usage and negligible CO 2 , the oxidative depolymerization of XL to produce HA shows high utilization efficiency of carbon, and is a promising clean and efficient utilization approach.</description><identifier>ISSN: 0361-5219</identifier><identifier>EISSN: 1934-8029</identifier><identifier>DOI: 10.3103/S0361521921050086</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Aromatic compounds ; Carbon dioxide ; Chemistry ; Chemistry and Materials Science ; Depolymerization ; High temperature ; Humic acids ; Lignite ; Molecular structure ; NMR ; Nuclear magnetic resonance ; Physical Chemistry ; Utilization</subject><ispartof>Solid fuel chemistry, 2021-09, Vol.55 (5), p.348-356</ispartof><rights>Allerton Press, Inc. 2021. 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Q.</creatorcontrib><creatorcontrib>Wang, Q.</creatorcontrib><creatorcontrib>Pan, C. X.</creatorcontrib><creatorcontrib>Yan, J. C.</creatorcontrib><creatorcontrib>Li, Z. K.</creatorcontrib><creatorcontrib>Lei, Z. P.</creatorcontrib><creatorcontrib>Ren, S. B.</creatorcontrib><creatorcontrib>Wang, X. L.</creatorcontrib><creatorcontrib>Kang, S. G.</creatorcontrib><creatorcontrib>Shui, H. F.</creatorcontrib><title>Efficient Oxidative Depolymerization of Xilinguole Lignite to Produce Humic Acids with Little CO2 Production</title><title>Solid fuel chemistry</title><addtitle>Solid Fuel Chem</addtitle><description>At present, non-fuel utilization as alternative chemical feedstocks becomes very important and significant for the efficient conversion of lignite. To reduce CO 2 production, an oxy-cracking technique in weak alkaline aqueous was conducted to selectively depolymerize Xilinguole lignite (XL) into humic acid (HA) under mild condition in this paper. The results indicated that XL has high reactivity, and can be depolymerized into HA with very little CO 2 . Elevated temperature is favorable for cracking of XL and converting HA into small molecular water-soluble acids and CO 2 . KOH mainly catalyzes the oxidative depolymerization of XL macromolecular structure. Lower temperature can reduce the formation of CO 2 and the usage of alkali. Under 80°C, KOH/XL = 0.33 and 2 h, HA weight yield was the highest, reaching 81%, as well as no CO 2 detected. Further, the obtained HA was separated and characterized by FTIR, CPMAS 13 C-NMR, TG/DTG and element analyses. Compared to XL and oxidized residue, HA contains more OH and COOH groups and aromatic rings, and less aliphatic groups. Due to low alkali usage and negligible CO 2 , the oxidative depolymerization of XL to produce HA shows high utilization efficiency of carbon, and is a promising clean and efficient utilization approach.</description><subject>Aromatic compounds</subject><subject>Carbon dioxide</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Depolymerization</subject><subject>High temperature</subject><subject>Humic acids</subject><subject>Lignite</subject><subject>Molecular structure</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Physical Chemistry</subject><subject>Utilization</subject><issn>0361-5219</issn><issn>1934-8029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kFFLwzAUhYMoOKc_wLeAz9WbpEnbxzGnEwYTVPCttGkyM7pmJqk6f70pG_ggPt3LPd85Fw5ClwSuGQF28wRMEE5JQQlwgFwcoREpWJrkQItjNBrkZNBP0Zn3awDOixxGqJ1pbaRRXcDLL9NUwXwofKu2tt1tlDPf8WA7bDV-Na3pVr1tFV6YVWeCwsHiR2ebXio87zdG4ok0jcefJrxFJoSITpf0wAw55-hEV61XF4c5Ri93s-fpPFks7x-mk0UiGREhyYRqtBJprakmKU8zXYtKi1pzxqFiXFCWpXEVtNGyyKq8VkBzCjyVKs0Lycboap-7dfa9Vz6Ua9u7Lr4sKc9jCYwWECmyp6Sz3july60zm8rtSgLlUGr5p9TooXuPj2y3Uu43-X_TD4waeN4</recordid><startdate>20210901</startdate><enddate>20210901</enddate><creator>Wang, Z. 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K.</creatorcontrib><creatorcontrib>Lei, Z. P.</creatorcontrib><creatorcontrib>Ren, S. B.</creatorcontrib><creatorcontrib>Wang, X. L.</creatorcontrib><creatorcontrib>Kang, S. G.</creatorcontrib><creatorcontrib>Shui, H. F.</creatorcontrib><collection>CrossRef</collection><jtitle>Solid fuel chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Z. C.</au><au>Wu, Z. Q.</au><au>Wang, Q.</au><au>Pan, C. X.</au><au>Yan, J. C.</au><au>Li, Z. K.</au><au>Lei, Z. P.</au><au>Ren, S. B.</au><au>Wang, X. L.</au><au>Kang, S. G.</au><au>Shui, H. F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Oxidative Depolymerization of Xilinguole Lignite to Produce Humic Acids with Little CO2 Production</atitle><jtitle>Solid fuel chemistry</jtitle><stitle>Solid Fuel Chem</stitle><date>2021-09-01</date><risdate>2021</risdate><volume>55</volume><issue>5</issue><spage>348</spage><epage>356</epage><pages>348-356</pages><issn>0361-5219</issn><eissn>1934-8029</eissn><abstract>At present, non-fuel utilization as alternative chemical feedstocks becomes very important and significant for the efficient conversion of lignite. To reduce CO 2 production, an oxy-cracking technique in weak alkaline aqueous was conducted to selectively depolymerize Xilinguole lignite (XL) into humic acid (HA) under mild condition in this paper. The results indicated that XL has high reactivity, and can be depolymerized into HA with very little CO 2 . 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subjects Aromatic compounds
Carbon dioxide
Chemistry
Chemistry and Materials Science
Depolymerization
High temperature
Humic acids
Lignite
Molecular structure
NMR
Nuclear magnetic resonance
Physical Chemistry
Utilization
title Efficient Oxidative Depolymerization of Xilinguole Lignite to Produce Humic Acids with Little CO2 Production
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