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- 저자 : Ji-lai Zhou (검색결과 3 건)
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Bo Lai,Qingqing Ji,Yue Yuan,Donghai Yuan,Yuexi Zhou,Juling Wang 한국화학공학회 2016 Korean Journal of Chemical Engineering Vol.33 No.1
To investigate the degradation of high concentration pollutant by Fe/Cu bimetallic system at a high operating temperature, 10,000mg/L acid orange 7 (AO7) aqueous solution was treated by Fe/Cu bimetallic system at 80 oC. First, the effect of the operating temperature (30-80 oC) on the reactivity of Fe/Cu bimetallic particles was investigated thoroughly. Then, the studies on the effect of theoretical Cu mass loading, Fe/Cu dosage, stirring speed and initial pH on the reactivity of Fe/Cu bimetallic particles at a high temperature (i.e., 80 oC) were carried out, respectively. The degradation and transformation process of AO7 was studied by using COD, TOC and UV-Vis spectra. The results indicate that high concentration pollutant could be removed effectively by Fe/Cu bimetallic system at a high operating temperature. And the removal efficiencies of AO7 by Fe/Cu bimetallic system were in accordance with the pseudofirst- order model. Finally, it was observed that the high temperature could accelerate mass transport rate and overcome the high activation energy barrier to significantly improve the reactivity of Fe/Cu bimetallic particles. Therefore, the higher removal efficiency could be obtained by Fe/Cu system at a high operating temperature. Thus, the high operating temperature played a leading role in the degradation of high concentration pollutant.
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Zhu Wentao,Zhou Juan,Lu Shan,Yang Jing,Lai Xin-He,Jin Dong,Pu Ji,Huang Yuyuan,Liu Liyun,Li Zhenjun,Xu Jianguo 한국미생물학회 2022 The journal of microbiology Vol.60 No.2
Four novel Gram-negative, mesophilic, aerobic, motile, and cocci-shaped strains were isolated from tick samples (strains 546T and 573) and respiratory tracts of marmots (strains 1318T and 1311). The 16S rRNA gene sequencing revealed that strains 546T and 573 were 97.8% identical to Roseomonas wenyumeiae Z23T, whereas strains 1311 and 1318T were 98.3% identical to Roseomonas ludipueritiae DSM 14915T. In addition, a 98.0% identity was observed between strains 546T and 1318T. Phylogenetic and phylogenomic analyses revealed that strains 546T and 573 clustered with R. wenyumeiae Z23T, whereas strains 1311 and 1318T grouped with R. ludipueritiae DSM 14915T. The average nucleotide identity between our isolates and members of the genus Roseomonas was below 95%. The genomic G+C content of strains 546T and 1318T was 70.9% and 69.3%, respectively. Diphosphatidylglycerol (DPG) and phosphatidylethanolamine (PE) were the major polar lipids, with Q-10 as the predominant respiratory quinone. According to all genotypic, phenotypic, phylogenetic, and phylogenomic analyses, the four strains represent two novel species of the genus Roseomonas, for which the names Roseomonas haemaphysalidis sp. nov. and Roseomonas marmotae sp. nov. are proposed, with 546T (= GDMCC 1.1780T = JCM 34187T) and 1318T (= GDMCC 1.1781T = JCM 34188T) as type strains, respectively.
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Liu-Jing Wei,Ji-lai Zhou,Dan-ni Zhu,Bai-yi Cai,Jin-Ping Lin,Qiang Hua,Dong-Zhi Wei 한국생물공학회 2012 Biotechnology and Bioprocess Engineering Vol.17 No.6
In this study a new insight was provided to understand the functions of membrane-bound alcohol dehydrogenase (mADH) and aldehyde dehydrogenase (mALDH) in the bio-oxidation of primary alcohols, diols and poly alcohols using the resting cells of Gluconobacter oxydans DSM 2003 and its mutant strains as catalyst. The results demonstrated that though both mADH and mALDH participated in most of the oxidation of alcohols to their corresponding acid, the exact roles of these enzymes in each reaction might be different. For example,mADH played a key role in the oxidation of diols to its corresponding organic acid in G. oxydans, but it was dispensable when the primary alcohols were used as substrates. In contrast to mADH, mALDH appears to play a relatively minor role in organic acid-producing reactions because of the possible presence of other isoenzymes. Aldehydes were, however, found to be accumulated in the mALDH-deficient strain during the oxidation of alcohols.
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