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341.
耐盐菌GTY对偶氮染料活性艳红X-3B的脱色研究   总被引:2,自引:0,他引:2  
为了选择耐盐菌GTY对偶氮染料活性艳红X-3B的最佳脱色条件,研究了不同环境条件对脱色效果的影响,结果表明耐盐菌GTY对偶氮染料活性艳红X-3B有较好的脱色效果,能够适应较宽范围的pH值以及污染物负荷,当pH值在7~9之间,活性艳红X-3B初始浓度在600mg/L以下,GTY菌液生长期在对数末期时脱色效果达到最佳状态,24h脱色率能达到90%左右。同时考察了GTY的不同初始接菌量对活性艳红X-3B脱色的影响,结果发现高的初始接菌量可以提高脱色速率,但是一定时间后,初始接菌量对最终脱色效果并无太大影响,兼顾节约成本和脱色效果选择最佳初始接菌量为5%。  相似文献   
342.
以钛酸丁酯为前驱体,采用溶胶-凝胶法制备TiO2,将TiO2与Fenton试剂联合用来处理酸性红B模拟废水,研究了在紫外光条件下的降解效果,确定最佳反应条件.实验结果表明,采用TiO2与Fenton试剂联合的方式对酸性红B染料废水进行处理,其降解效果明显优于单一使用TiO2和Fenton法的处理方式.对于初始浓度为100 mg/L的酸性红B模拟染料废水,在TiO2投加量为1 g/L,pH为3,Fe2+为0.15 mmol/L,H2O2为1mmol/L,UV光照时间为60 min时,脱色率可达最佳.  相似文献   
343.
This paper aimed to find an efficient bacterium for decolorizing azo dyes. A strain which could decolorize Congo Red efficiently was isolated from Congo Red. The strain was identified as Paenibacillus dendritiformis GGJ7 (GGJ7, in short) by 16S rRNA gene sequence (NCBI accession No. KY655213). Strain GGJ7 was applied to the decolorization of azo dyes in this research, and influencing factors of decolorization were investigated, including diverse nutritional conditions, culture conditions (pH, temperature, oxygen conditions), and various dyes. The results demonstrated that the decolorization rate of Congo Red by strain GGJ7 was much higher than that of the other eight strains (e.g., YRJ1, YRJ2 etc.) in our previous work. The optimal conditions for Congo Red decolorization were 25 g/L LB broth as nutrient source, 30 °C, pH 7, and an anaerobic environment. The mechanism of decolorization was mainly biodegradation, and the decolorization process of strain GGJ7 was conformed to the first-class kinetics model: -ln (At /A0) = 0.6058t - 0.1082. For different azo dyes, the decolorization rate was up to 95%. Strain GGJ7 only needed 1 h to decolorize 50 mg/L Methyl Orange, 25 mg/L Croceine Scarlet, and 25 mg/L Methyl Red, needed 3 h to decolorize 50 mg/L Orange G and 50 mg/L Orange G6, and needed 4 h to decolorize 50 mg/L Congo Red. In summary, strain GGJ7 is an efficient azo dye-decolorizing bacterium, and it has a potential application in treating printing and dyeing wastewater. © 2018 Science Press. All rights reserved.  相似文献   
344.
• The optimum SCR activity was realized by tuning the acid pretreatment. • Optimized catalysts showed NOx conversion above 90%. • The NH3 and NO adsorption capacity of Al-O3-Fe is stronger than Fe-O3-Fe. • The formation of almandine consumes Fe3+ and Al3+ and weakens their interaction. Red mud (RM), as an alkaline waste, was recently proved to be a promising substitute for the SCR catalyst. Dealkalization could improve the acidity and reducibility of red mud, which were critical for SCR reaction. However, the dealkalization effect depended on the reaction between acid solution and red mud. In this study, we realized the directional control of the chemical state of active sites through tuning the acid pretreatment (dealkalization) process. The pretreatment endpoint was controlled at pH values of 3–5 with diluted nitric acid. When the pH values of red mud were 3 and 5 (CRM-3 and CRM-5), activated catalysts showed NOx conversion above 90% at 275°C–475°C. The high initial reaction rate, Ce3+/(Ce3+ + Ce4+) ratio, and surface acidity accounted for the excellent SCR performance of CRM-5 catalyst. Meanwhile, more Fe3+ on the CRM-3 surface improved the NH3 adsorption. There was a strong interaction between Al and Fe in both CRM-5 and CRM-3 catalysts. DFT results showed that the adsorption capacity of the Al-O3-Fe for NH3 and NO is stronger than that of Fe-O3-Fe, which enhanced the NOx conversion of the catalyst. However, the almandine was formed in CRM-4, consumed part of Fe3+ and Al3+, and the interaction between Al and Fe was weakened. Also, deposited almandine on the catalyst surface covered the active sites, thus leading to lower NH3-SCR activity.  相似文献   
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