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The objectives of the project were to isolate a bacterial strain capable of degrading pentyl amine and aniline and to define the optimal pentyl amine and aniline degradation conditions for this bacterial strain. The bacterial strain was isolated from activated sludge obtained from a Northeastern China treatment facility for petrochemical wastewater rich in pentyl amine and aniline. Once the strain was isolated, five triplicate (5) batch tests were used to establish the conditions for maximum pentyl amine and aniline degradation, by varying one at a time the following five factors: temperature, pH, reaction time, pollutant concentrations and aeration rate. In a final test, oil refinery sludge was inoculated with the strain and tested for the degradation of pentyl amine and aniline under optimal conditions, while observing the degradation pathway of pentyl amine and aniline. The isolated strain, PN1001, is a member of the Pseudomonas species and it was capable of degrading pentyl amine and aniline. The optimal reactor conditions for the degradation of a mixture of pentyl amine and aniline, at a concentration ranging between 150 and 200mg/L, were found to be 30 degrees C at a pH of 7.0, under a reaction time of 24h and a maximum solution dissolved oxygen level of 6 mgO(2)/L. Under such conditions, the strain PN1001 degraded 93% and 89% of the pentyl amine and aniline, respectively, aniline being more toxic and demonstrating a more complex degradation pathway. The strain PN1001 degraded more contaminants when both were present because of the pi and sigma electron cloud coordination functions of aniline and pentyl amine, respectively, presumed to reduce the toxic effect of aniline. Once inoculated with the strain, oil refinery sludge degraded 93% and 88% of the pentyl amine and aniline, compared to the strain alone which degraded 72% and 82%, likely because of the sludge's buffering effect against the toxic environment. 相似文献
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Aniline degradation by electrocatalytic oxidation 总被引:4,自引:0,他引:4
The degradation of aniline solution in alkaline medium of pH 11.0 by electrocatalytic oxidation has been studied using an electrochemical reactor containing a SnO2–Sb2O3–PtO anode and a Ti cathode, both of 54 cm2 area. Hydroxyl radicals (HO√) are produced at the anode, being tested with the trace catcher salicylic acid and phenol by spectrophotometery and high performance liquid chromatography. Intermediates dianiline, 4-anilino phenol and azobenzol were detected by gas chromatography–mass spectrometry. The existence of HO√ produced in the aniline degradation was assayed with scavenger tertiary butanol. The results showed that electrocatalytic oxidation is an effective process for the degradation of aniline. A general reaction pathway that accounts for aniline degradation to CO2 involving those intermediates is proposed. 相似文献
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The effect of the surfactant template cetyltrimethylammonium bromide (CTAB) in MCM-41 on the adsorption of aniline was investigated. Various MCM-41 samples were prepared by controlling template removal using an extraction method. The samples were then used as adsorbents for the removal of aniline from aqueous solution. The results showed that the MCM-41 samples with the template partially removed (denoted as C-MCM-41) exhibited better adsorption performance than MCM-41 with the template completely removed (denoted as MCM-41). The reason for this difference may be that the C-MCM-41 samples had stronger hydrophobic properties and selectivity for aniline because of the presence of the template. The porosity and cationic sites generated by the template play an important role in the adsorption process. The optimal adsorbent with moderate template was achieved by changing the ratio of extractant; it has the potential for promising applications in the field of water pollution control. 相似文献
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顶空气相色谱法快速测定土壤中苯、苯胺和硝基苯 总被引:1,自引:0,他引:1
采用顶空气相色谱法快速测定土壤中苯、苯胺和硝基苯,优化了试验条件.方法在0 mg/L~100 mg/L范围内线性良好,苯、苯胺、硝基苯的检出限分别为0.012 mg/kg、0.22 mg/kg、0.083 mg/kg,实际土样测定的RSD≤1.4%,加标回收率为94.0%~102%. 相似文献
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气相色谱法测定废水中苯胺类化合物 总被引:4,自引:0,他引:4
建立了气相色谱测定废水中5种苯胺类化合物的方法,优化了试验条件。方法在0mg/L-100mg/L之间线性关系良好,N,N-二甲苯胺、苯胺、对甲苯胺、间甲苯胺、邻甲苯胺的检出限分别为0.004mg/L、0.002mg/L、0.013mg/L、0.008mg/L、0.007mg/L,实际废水样品测定的RSD≤1.5%,加标回收率为93.8%~99.5%。 相似文献