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1.
真菌修复砷污染土壤是一种能够有效吸附固化环境中砷的重要措施.生物炭作为目前修复重金属的热点,其多空疏松的结构、较高的离子交换量、丰富的有机碳含量等都说明了其在土壤修复中的地位.为了探究生物炭与青霉菌在修复砷污染土壤的同时对土壤中微生物活性及其多样性的影响,在室内孵育条件下,运用Biolog法研究了3×3随机区组试验(3个生物炭梯度分别为0%、2%、4%,3个青霉菌梯度分别为0%、10%、20%)下土壤微生物对不同类型碳源的利用能力以及多种功能性指数的影响.结果表明:①添加青霉菌与生物炭后,土壤中有效砷含量较对照组显著下降,从而影响其微生物群落功能多样性.②砷污染土壤中微生物群落功能多样性、碳源利用丰富度随生物炭浓度梯度的升高呈先升后降的趋势.③高接菌量(20%)与低接菌量(10%)对砷污染土壤中微生物群落功能多样性的影响没有显著性差异.④2%生物炭与10%青霉菌处理土壤中微生物群落功能多样性、碳源利用丰度最高.⑤青霉菌对胺类及少部分酸类碳源的利用能力较弱(AWCD < 0.5,AWCD为Biolog微平板孔中溶液吸光值平均颜色变化率),对氨基酸类中大部分碳源以及脂类碳源的代谢能力较强(AWCD>1.0),对糖类、酚酸类的代谢能力稍弱(AWCD为0.3~1.0),青霉菌对D-半乳糖醛酸、L-天冬酰胺酸、L-丝氨酸、L-精氨酸、r-羟基丁酸这5种碳源的利用率最高(AWCD>1.2).研究显示,低浓度生物炭可增加砷污染土壤中微生物群落多样性,生物炭含量的继续增加会对微生物产生抑制作用;青霉菌添加到砷污染土壤后,会显著提升砷污染土壤中微生物的群落功能多样性,改善砷污染土壤中微生的物群落结构;青霉菌的优势碳源大多为植物根系分泌物,可为后续青霉菌与超积累植物复合修复砷污染土壤提供参考. 相似文献
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Huang Jingyu Opoku Prince Atta Guang Li Ke Li Norgbey Eyram 《Environmental science and pollution research international》2021,28(46):65399-65409
Environmental Science and Pollution Research - To achieve allowable gas emission limits and eliminate the high cost and challenges associated with pre-treatment of sludge before incineration, a new... 相似文献
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Jingyu Su Guanping Jin Changyong Li Xiaohui Zhu Yan Dou Yong Li Xin Wang Kunwei Wang Qianqian Gu 《环境科学学报(英文版)》2014,26(11):2355-2361
Ni was effectively recovered from spent electroless nickel (EN) plating baths by forming a nano-nickel coated activated carbon composite. With the aid of ultrasonication, melamine- formaldehyde-tetraoxalyl-ethylenediamine chelating resins were grafted on activated carbon (MFT/AG). PdC12 sol was adsorbed on MFT/AC, which was then immersed in spent electroless nickel plating bath; then nano-nickel could be reduced by ascorbic acid to form a nano-nickel coating on the activated carbon composite (Ni/AC) in situ. The materials present were carefully examined by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, X-ray photoelectron spectroscopy and electro- chemistry techniques. The resins were well distributed on the inside and outside surfaces of activated carbon with a size of 120 ± 30 nm in MFT/AC, and a great deal of nano-nickel particles were evenly deposited with a size of 3.8 ± 1.1 nm in Ni/MFT. Moreover, Ni/AC was successfully used as a catalyst for ultrasonic degradation of 2.6-dichloronhenol. 相似文献
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长三角地区大气污染治理取得一定成效,然而空气质量改善逐渐进入瓶颈期和攻坚期,大气污染治理战略需要从宏观层面系统谋划。本文系统分析了近10年来长三角区域经济、能源、产业、交通的发展状况和趋势,结合区域大气污染物浓度水平的演变,分析了大气污染与经济社会发展的耦合关系。结合当前区域空气污染的空间分布差异以及经济能源交通结构的内在差别,识别了大气污染的区内差异特征及关键制约因素。在此基础上,从能源结构和产业结构调整、交通结构优化、分区施策、深化治理等角度,为深化区域大气污染联防联控,持续改善大气污染问题提出了政策建议。 相似文献
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Facile, effective, and environment-friendly degradation of sulfamonomethoxine in aqueous solution with the aid of a UV/Oxone oxidative process 总被引:1,自引:0,他引:1
Yunqing Pi Jinglan Feng Jingyu Sun Jianhui Sun 《Environmental science and pollution research international》2013,20(12):8621-8628
The degradation of sulfamonomethoxine (SMM) in the aqueous environment by the combination of UV illumination and Oxone has been studied. Experimental results indicated that the UV illumination can effectively activate Oxone to produce sulfate-free radicals (SO4 ??). When 10 mmol L?1 Oxone was added, 96.78 % removal of SMM (5 mg L?1) was achieved within 90 min. Mineralization of SMM was investigated by measuring the total organic carbon, which decreased by 89.01 % after 90 min reaction. Six intermediate compounds generated during the SMM degradation were identified with the aid of liquid chromatography and mass spectroscopy, combined with proton nuclear magnetic resonance spectroscopy. A general reaction pathway for the degradation of SMM was proposed, where the presence of SO4 ?? remained crucial during the degradation process. 相似文献
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Yunqing Pi Jinglan Feng Jingyu Sun Mengke Song Jianhui Sun 《Environmental science and pollution research international》2014,21(4):3031-3040
Oxidative degradation of ofloxacin (OFX) by sulfate free radicals (SO4 ??) in the UV/Oxone/Co2+oxidation process was investigated for the first time, with a special focus upon identifying the transformation products as well as understanding the reaction pathways. Thirteen main compounds were identified after the initial transformation of OFX; the detailed structural information of which were characterized by high-performance liquid chromatography–high resolution mass spectrometry and MS fragmentation analysis. The degradation pathways mainly encompassed ring openings at both the piperazinyl substituent and the quinolone moiety, indicating that the usage of SO4 ?? aided the oxidative degradation of OFX to undergo more facile routes compared to those in previous reports by using OH?/h+ as the oxidant, where the initial transformation attacks were mainly confined to the piperazine moiety. Moreover, in this study, smart control over the pH conditions of the oxidation system via different modes of Oxone dosage resulted in the selective degradation of the functional sites of OFX molecule, where it was shown that the SO4 ??-driven destruction of the quinolone moiety of OFX molecule favored the neutral pH conditions. This would be beneficial for the reduction of bacterial resistance against quinolones in the aqueous environment. 相似文献
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