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首页> 外文期刊>Chemosphere >Combined effect of adsorption and biodegradation of biological activated carbon on H_2S biotrickling filtration
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Combined effect of adsorption and biodegradation of biological activated carbon on H_2S biotrickling filtration

机译:生物活性炭吸附与生物降解联合作用对H_2S生物滴滤的影响

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摘要

In order to evaluate the combined effect of adsorption and biodegradation of H_2S on activated carbon surface in biotrickling filtration, four laboratory-scale biofiltration columns were operated simultaneously for 120 h to investigate the mechanisms involved in treating synthetic H_2S streams using biological activated carbon (BAC). The first three columns (A, B, C) contained a mixture of activated carbon and glass beads, with the carbons (BAC or virgin activated carbon (VAC)) and conditions (with or without liquid medium recir-culation) differentiated. The last column (D) used 100% glass beads with liquid medium recirculation. Air streams containing 45 ppmv H_2S were passed through the columns at 4 s of gas retention time (GRT) and liquid flow rate was set at 0.71 ml min~(-1). Column D got its breakthrough in 3 min of operation, indicating a negligible contribution of glass beads to the adsorption of H_2S. The removal efficiency (RE) of Columns B and C using VAC dropped quickly to 30% within the first 8 h, and afterwards continued to drop further but slowly. Column A using BAC stayed at 25% of RE throughout the operation time. A thorough investigation of the H_2S oxidation products, i.e., various S species in both aqueous (recirculation media) and solid phases (BAC and VAC), was conducted using ICP-OES, IC, XRF, and CHNS elemental analyzer. BAC demonstrated a better performance than columns with adsorption only. Water film was found to enhance H_2S removal. The percentage of sulphate in the total sulphur of the BAC system improved to twice of that of VAC system, indicating sulphate is the main product of H_2S biofiltration. The observed pH drop in BAC system double confirmed that the presence of biodegradation in the biofilm over carbon surface did profound effect on the oxidation of H_2S, compare to the systems with adsorption only.
机译:为了评估生物滴滤中活性炭表面上H_2S的吸附和生物降解的综合作用,同时操作四个实验室规模的生物滤柱120 h,以研究利用生物活性炭(BAC)处理合成H_2S物流的机理。 。前三列(A,B,C)包含活性炭和玻璃珠的混合物,并区分了碳(BAC或原始活性炭(VAC))和条件(有或没有液态介质循环调节)。最后一列(D)使用100%玻璃珠,其中液体介质再循环。含有45 ppmv H_2S的气流在气体保留时间(GRT)的4 s内通过色谱柱,液体流速设置为0.71 ml min〜(-1)。 D柱在运行3分钟后获得突破,表明玻璃珠对H_2S的吸附作用可忽略不计。使用VAC的B和C色谱柱的去除效率(RE)在最初的8小时内迅速下降至30%,此后继续下降,但缓慢。在整个操作过程中,使用BAC的A柱保持在RE的25%。使用ICP-OES,IC,XRF和CHNS元素分析仪对H_2S氧化产物,即水相(再循环介质)和固相(BAC和VAC)中的各种S物种进行了全面研究。 BAC表现出比仅吸附柱更好的性能。发现水膜增强了H_2S的去除。 BAC系统总硫中的硫酸盐百分比提高到VAC系统的两倍,这表明硫酸盐是H_2S生物过滤的主要产物。与仅具有吸附的系统相比,在BAC系统中观察到的pH下降双倍证实了生物膜在碳表面上生物降解的存在对H_2S的氧化产生了深远的影响。

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