{"title":"褐煤热改性对水分再吸附的影响机理","authors":"Lei Fan, Chuanzhi Hu, Huimin Gong, Qinghai Ren, Xingshuai Fan, Xin Cheng","doi":"10.1680/jemmr.22.00001","DOIUrl":null,"url":null,"abstract":"The influence mechanism of lignite thermal upgrading on moisture re-adsorption was investigated using analytical instruments as DTA-TG, FTIR, SEM. The results showed that the moisture content of lignite decreased from 44.78% to 25.07% through the drying process. After the moisture in the lignite and the air reached a dynamic equilibrium, the moisture content of the lignite was 25.75 wt.%. The characteristic functional groups of lignite include hydroxyl, methylene, methyl, carbonyl, carboxyl and ether oxygen. The adsorption distances of the five adsorption sites of carboxyl, phenolic hydroxyl, alcoholic hydroxyl, carbonyl and ether bond to water molecules were 2.081 Å, 2.933 Å, 1.905 Å, 1.860 Å and 1.881 Å, respectively. The order of the adsorption strength of water molecules on the characteristic functional groups was: Carbonyl>Phenolic hydroxyl>Ether oxygen >Alcoholic hydroxyl>Carboxyl. During the upgrading by drying process, the characteristic functional groups that were prone to hydrogen bonds of water molecules partially decomposed. The reduction of pores and the partial decomposition of hydrophilic functional groups after upgrading in the lignite structure made the adsorption capacity of lignite to water molecules weakened. Therefore, the re-absorption of water molecules by lignite was reduced.","PeriodicalId":11537,"journal":{"name":"Emerging Materials Research","volume":" ","pages":""},"PeriodicalIF":1.3000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The influence mechanism of lignite thermal upgrading on moisture re-adsorption\",\"authors\":\"Lei Fan, Chuanzhi Hu, Huimin Gong, Qinghai Ren, Xingshuai Fan, Xin Cheng\",\"doi\":\"10.1680/jemmr.22.00001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The influence mechanism of lignite thermal upgrading on moisture re-adsorption was investigated using analytical instruments as DTA-TG, FTIR, SEM. The results showed that the moisture content of lignite decreased from 44.78% to 25.07% through the drying process. After the moisture in the lignite and the air reached a dynamic equilibrium, the moisture content of the lignite was 25.75 wt.%. The characteristic functional groups of lignite include hydroxyl, methylene, methyl, carbonyl, carboxyl and ether oxygen. The adsorption distances of the five adsorption sites of carboxyl, phenolic hydroxyl, alcoholic hydroxyl, carbonyl and ether bond to water molecules were 2.081 Å, 2.933 Å, 1.905 Å, 1.860 Å and 1.881 Å, respectively. The order of the adsorption strength of water molecules on the characteristic functional groups was: Carbonyl>Phenolic hydroxyl>Ether oxygen >Alcoholic hydroxyl>Carboxyl. During the upgrading by drying process, the characteristic functional groups that were prone to hydrogen bonds of water molecules partially decomposed. The reduction of pores and the partial decomposition of hydrophilic functional groups after upgrading in the lignite structure made the adsorption capacity of lignite to water molecules weakened. Therefore, the re-absorption of water molecules by lignite was reduced.\",\"PeriodicalId\":11537,\"journal\":{\"name\":\"Emerging Materials Research\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Emerging Materials Research\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1680/jemmr.22.00001\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Emerging Materials Research","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1680/jemmr.22.00001","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
The influence mechanism of lignite thermal upgrading on moisture re-adsorption
The influence mechanism of lignite thermal upgrading on moisture re-adsorption was investigated using analytical instruments as DTA-TG, FTIR, SEM. The results showed that the moisture content of lignite decreased from 44.78% to 25.07% through the drying process. After the moisture in the lignite and the air reached a dynamic equilibrium, the moisture content of the lignite was 25.75 wt.%. The characteristic functional groups of lignite include hydroxyl, methylene, methyl, carbonyl, carboxyl and ether oxygen. The adsorption distances of the five adsorption sites of carboxyl, phenolic hydroxyl, alcoholic hydroxyl, carbonyl and ether bond to water molecules were 2.081 Å, 2.933 Å, 1.905 Å, 1.860 Å and 1.881 Å, respectively. The order of the adsorption strength of water molecules on the characteristic functional groups was: Carbonyl>Phenolic hydroxyl>Ether oxygen >Alcoholic hydroxyl>Carboxyl. During the upgrading by drying process, the characteristic functional groups that were prone to hydrogen bonds of water molecules partially decomposed. The reduction of pores and the partial decomposition of hydrophilic functional groups after upgrading in the lignite structure made the adsorption capacity of lignite to water molecules weakened. Therefore, the re-absorption of water molecules by lignite was reduced.
期刊介绍:
Materials Research is constantly evolving and correlations between process, structure, properties and performance which are application specific require expert understanding at the macro-, micro- and nano-scale. The ability to intelligently manipulate material properties and tailor them for desired applications is of constant interest and challenge within universities, national labs and industry.