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两种固定化微生物材料对石油烃降解及演化特性的研究

Study of the Characteristics of Two Immobilized Microbial Materials in Degradation and Evolution of Petroleum Hydrocarbon.

作者信息

Luo Xiaofang, Chen Lihua, Zhao Shujing, Lei Zhongchun, Xia Miaomiao, Zhang Chuantao

机构信息

Experimental Teaching Department, Northwest Minzu University, Lanzhou 730030, P. R China.

College of Chemical Engineering, Key Laboratory for Utility of Environment-Friendlymicro Composite Materials and Biomass in University of Gansu Province, Northwest Minzu University, Lanzhou, Gansu 730030, P. R China.

出版信息

ACS Omega. 2020 Jul 29;5(31):19402-19408. doi: 10.1021/acsomega.0c01123. eCollection 2020 Aug 11.

DOI:10.1021/acsomega.0c01123
PMID:32803033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7424575/
Abstract

To enhance the degradation efficiency of oily wastewater, polyacrylamide (PAM)-sodium alginate (SA) and poly(vinyl alcohol) (PVA)-sodium alginate (SA) were mixed and used as spherical supporting materials for the immobilization of microbials, which were employed as a platform to study the degradation of total petroleum hydrocarbons (TPHs) in the oily wastewater. The degradation and evolution of normal paraffin (n-paraffin) series have been studied by determining the crude oil group composition of the residual oils by the gas chromatography-mass spectrometry (GC-MS) analysis. The results show that the half-lives of the PAM-SA-immobilized microorganisms are 6.21 days, which is 2.11 days less than that of PVA-SA, indicating that more nutrients are provided by PAM-SA for microbial growth, which can accelerate the degradation of TPHs. As can be seen from the GC-MS analysis, the main peak carbons of the n-paraffin series are moved backward after 14 days of degradation, implying the degrading advantage of n-paraffin with low carbon numbers. The ∑C21/∑C22 value of PAM-SA was measured to be 0.749, which is greater than that of PVA-SA (0.051), indicating that PAM-SA has a superior ability to degrade normal paraffins with high carbon numbers. After 14 days of degradation, an odd-even predominance (OEP) (the mass ratio of normal alkanes of odd carbon/even carbon) value of 1.075 for PAM-SA was obtained, which is slightly larger than that of PVA-SA (0.967), indicating a better degradation performance of PAM-SA, especially for the degradation of the even-carbon normal paraffins with high carbon numbers. The Pr/Ph of PAM-SA is 0.938, which is also greater than that of PVA-SA (0.844), indicating that the ability of PAM-SA for the degradation of isoprenoids is superior to that of PVA-SA under the immobilized conditions. Based on these results, in terms of immobilization of microorganisms, PAM-SA, instead of PVA-SA, is more advantageous for the degradation of TPH in the oily wastewater.

摘要

为提高含油废水的降解效率,将聚丙烯酰胺(PAM)-海藻酸钠(SA)和聚乙烯醇(PVA)-海藻酸钠(SA)混合用作固定化微生物的球形载体材料,以此作为研究含油废水中总石油烃(TPHs)降解的平台。通过气相色谱-质谱联用(GC-MS)分析确定残留油的原油族组成,研究了正构烷烃系列的降解与演化。结果表明,PAM-SA固定化微生物的半衰期为6.21天,比PVA-SA的半衰期短2.11天,这表明PAM-SA为微生物生长提供了更多养分,可加速TPHs的降解。从GC-MS分析可以看出,降解14天后,正构烷烃系列的主峰碳向后移动,这意味着低碳数正构烷烃具有降解优势。测得PAM-SA的∑C21/∑C22值为0.749,大于PVA-SA的(0.051),表明PAM-SA具有更强的降解高碳数正构烷烃的能力。降解14天后,PAM-SA的奇偶优势(OEP)(奇数碳正构烷烃与偶数碳正构烷烃的质量比)值为1.075,略大于PVA-SA的(0.967),表明PAM-SA的降解性能更好,尤其是对高碳数偶数碳正构烷烃的降解。PAM-SA的Pr/Ph为0.938,也大于PVA-SA的(0.844),表明在固定化条件下,PAM-SA降解类异戊二烯的能力优于PVA-SA。基于这些结果,在微生物固定化方面,对于含油废水中TPH的降解,PAM-SA比PVA-SA更具优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/069678bd12a6/ao0c01123_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/d9fb2b854a6a/ao0c01123_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/6c5501d6b52a/ao0c01123_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/19c08e526a5c/ao0c01123_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/069678bd12a6/ao0c01123_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/d9fb2b854a6a/ao0c01123_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/6c5501d6b52a/ao0c01123_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/19c08e526a5c/ao0c01123_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97bf/7424575/069678bd12a6/ao0c01123_0004.jpg

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