{"title":"堆肥产生的溶解有机物对六价铬的还原作用。","authors":"Chuanghe Miao, Hui Rong, Xiaoqing Wei, Jianying Shang, Hu Zhou, Yizhong Lv","doi":"10.1039/d4em00280f","DOIUrl":null,"url":null,"abstract":"<p><p>Compost-derived dissolved organic matter (DOM<sub>C</sub>) is a heterogeneous assemblage of different redox-active organic molecules. We hypothesize that DOM<sub>C</sub> can interact with Cr(VI) and reduce it to Cr(III), thereby influencing the dynamics of Cr(VI) in soil and aquatic environments. Here, DOM<sub>C</sub>, along with soil humic substances isolated from red soil and black soil, were fractionated into humic acid fractions (<i>i.e.</i>, HA<sub>C</sub>, HA<sub>B</sub>, and HA<sub>R</sub>) and fulvic acid fractions (<i>i.e.</i>, FA<sub>C</sub>, FA<sub>B</sub>, and FA<sub>R</sub>), respectively. The reduction and interaction between Cr(VI) and the six organic matter fractions were investigated. The results showed that the total Cr(VI) reduction capacity (TRC) of the six organic matter fractions was 26.77-49.34 μM Cr(VI) per mg OM. The TRC of HA fractions was 35.54-49.34 μM Cr(VI) per mg OM, which exceeded that of FA fractions (26.77-31.29 μM Cr(VI) per mg OM). DOM<sub>C</sub> had a HA/FA ratio of 0.64, which was higher than that of black soil humic substance (0.59) and red soil humic substance (0.20). The sum of the TRC of DOM<sub>C</sub> was 35.57 μM Cr(VI) per mg OM, which was larger than that of black soil humic substance (32.87 μM Cr(VI) per mg OM) and red soil humic substance (33.01 μM Cr(VI) per mg OM). The TRC was positively correlated with TOC, TN, phenol C, alkyl C, and aromatic C contents and negatively correlated with E<sub>2</sub>/E<sub>3</sub>, O-alkyl C, and carboxyl C contents. The reduction of Cr(VI) at pH 6 was negligible, whereas 32-67% Cr(VI) was reduced at pH 2. The Cr(VI) reduction capacities (RC2, RC2, and RC6) at pH 2-6 were positively correlated (<i>R</i><sup>2</sup> > 0.71) with phenol C. Spectral analysis showed that there was no obvious complexation between Cr(VI) and the six organic matter fractions at pH 6, and thus the reduction of Cr(VI) was negligible, but solution pH could affect the accessibility of organic molecules to Cr(VI) and thus influence Cr(VI) reduction.</p>","PeriodicalId":74,"journal":{"name":"Environmental Science: Processes & Impacts","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reduction of hexavalent chromium by compost-derived dissolved organic matter.\",\"authors\":\"Chuanghe Miao, Hui Rong, Xiaoqing Wei, Jianying Shang, Hu Zhou, Yizhong Lv\",\"doi\":\"10.1039/d4em00280f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Compost-derived dissolved organic matter (DOM<sub>C</sub>) is a heterogeneous assemblage of different redox-active organic molecules. We hypothesize that DOM<sub>C</sub> can interact with Cr(VI) and reduce it to Cr(III), thereby influencing the dynamics of Cr(VI) in soil and aquatic environments. Here, DOM<sub>C</sub>, along with soil humic substances isolated from red soil and black soil, were fractionated into humic acid fractions (<i>i.e.</i>, HA<sub>C</sub>, HA<sub>B</sub>, and HA<sub>R</sub>) and fulvic acid fractions (<i>i.e.</i>, FA<sub>C</sub>, FA<sub>B</sub>, and FA<sub>R</sub>), respectively. The reduction and interaction between Cr(VI) and the six organic matter fractions were investigated. The results showed that the total Cr(VI) reduction capacity (TRC) of the six organic matter fractions was 26.77-49.34 μM Cr(VI) per mg OM. The TRC of HA fractions was 35.54-49.34 μM Cr(VI) per mg OM, which exceeded that of FA fractions (26.77-31.29 μM Cr(VI) per mg OM). DOM<sub>C</sub> had a HA/FA ratio of 0.64, which was higher than that of black soil humic substance (0.59) and red soil humic substance (0.20). The sum of the TRC of DOM<sub>C</sub> was 35.57 μM Cr(VI) per mg OM, which was larger than that of black soil humic substance (32.87 μM Cr(VI) per mg OM) and red soil humic substance (33.01 μM Cr(VI) per mg OM). The TRC was positively correlated with TOC, TN, phenol C, alkyl C, and aromatic C contents and negatively correlated with E<sub>2</sub>/E<sub>3</sub>, O-alkyl C, and carboxyl C contents. The reduction of Cr(VI) at pH 6 was negligible, whereas 32-67% Cr(VI) was reduced at pH 2. The Cr(VI) reduction capacities (RC2, RC2, and RC6) at pH 2-6 were positively correlated (<i>R</i><sup>2</sup> > 0.71) with phenol C. Spectral analysis showed that there was no obvious complexation between Cr(VI) and the six organic matter fractions at pH 6, and thus the reduction of Cr(VI) was negligible, but solution pH could affect the accessibility of organic molecules to Cr(VI) and thus influence Cr(VI) reduction.</p>\",\"PeriodicalId\":74,\"journal\":{\"name\":\"Environmental Science: Processes & Impacts\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-11-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental Science: Processes & Impacts\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1039/d4em00280f\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science: Processes & Impacts","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1039/d4em00280f","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Reduction of hexavalent chromium by compost-derived dissolved organic matter.
Compost-derived dissolved organic matter (DOMC) is a heterogeneous assemblage of different redox-active organic molecules. We hypothesize that DOMC can interact with Cr(VI) and reduce it to Cr(III), thereby influencing the dynamics of Cr(VI) in soil and aquatic environments. Here, DOMC, along with soil humic substances isolated from red soil and black soil, were fractionated into humic acid fractions (i.e., HAC, HAB, and HAR) and fulvic acid fractions (i.e., FAC, FAB, and FAR), respectively. The reduction and interaction between Cr(VI) and the six organic matter fractions were investigated. The results showed that the total Cr(VI) reduction capacity (TRC) of the six organic matter fractions was 26.77-49.34 μM Cr(VI) per mg OM. The TRC of HA fractions was 35.54-49.34 μM Cr(VI) per mg OM, which exceeded that of FA fractions (26.77-31.29 μM Cr(VI) per mg OM). DOMC had a HA/FA ratio of 0.64, which was higher than that of black soil humic substance (0.59) and red soil humic substance (0.20). The sum of the TRC of DOMC was 35.57 μM Cr(VI) per mg OM, which was larger than that of black soil humic substance (32.87 μM Cr(VI) per mg OM) and red soil humic substance (33.01 μM Cr(VI) per mg OM). The TRC was positively correlated with TOC, TN, phenol C, alkyl C, and aromatic C contents and negatively correlated with E2/E3, O-alkyl C, and carboxyl C contents. The reduction of Cr(VI) at pH 6 was negligible, whereas 32-67% Cr(VI) was reduced at pH 2. The Cr(VI) reduction capacities (RC2, RC2, and RC6) at pH 2-6 were positively correlated (R2 > 0.71) with phenol C. Spectral analysis showed that there was no obvious complexation between Cr(VI) and the six organic matter fractions at pH 6, and thus the reduction of Cr(VI) was negligible, but solution pH could affect the accessibility of organic molecules to Cr(VI) and thus influence Cr(VI) reduction.
期刊介绍:
Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.