Fontenot Eric J, Lee Young Haeng, Matthews Rosalyn D, Zhu Guangxuan, Pavlostathis Spyros G
School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta GA 30332-0512, USA.
Appl Biochem Biotechnol. 2003 Apr-Jun;109(1-3):207-25. doi: 10.1385/abab:109:1-3:207.
The objective of the present study was to assess the biological decolorization of an industrial, spent reactive dyebath and its three dye components (Reactive Blue 19 [RB 19], Reactive Blue 21 [RB 21], and Reactive Red 198 [RR 198]) under methanogenic conditions. Using a mixed, methanogenic culture, batch assays were performed to evaluate the rate and extent of color removal as well as any potential toxic effects. Overall, a high rate and extent of color removal (>10 mg/[L.h] and 88%, respectively) were observed in cultures amended with either RB 19 (an anthraquinone dye) or spent dyebath at an initial dye concentration of 300 mg/L (expressed as RB 19 equivalent) and 30 g/L of NaCl. Inhibition of acidogenesis and, to a larger degree, of methanogenesis resulting in accumulation of volatile fatty acids was observed in both RB 19- and spent dyebath-amended cultures. RB 21 (a phthalocyanine dye) and RR 198 (an azo dye) tested at an initial concentration of 300 mg/L did not result in any significant inhibition of the mixed methanogenic culture. Based on results obtained with cultures amended with RB 19 with and without NaCl, as well as a control culture amended with 30 g/L of NaCl, salt was less inhibitory than either RB 19 or the dyebath. Therefore, the toxic effect of the spent dyebath is at least partially attributed to its major dye component RB 19 and NaCl. Further testing of the effect of RB 19 decolorization products on the methanogenic activity in the absence of NaCl demonstrated that these products are much less inhibitory than the parent dye. Although color removal occurred despite the severe culture inhibition, biological decolorization of full-strength reactive spent dyebaths using methanogenic cultures in a repetitive, closed-loop system is not deemed feasible. For this reason, a fermentative and halotolerant culture was developed and successfully used in our laboratory for the decolorization of industrial reactive dyebaths with 100 g/L of NaCl.
本研究的目的是评估在产甲烷条件下工业废活性染料浴及其三种染料成分(活性蓝19 [RB 19]、活性蓝21 [RB 21]和活性红198 [RR 198])的生物脱色情况。使用混合产甲烷培养物进行批次试验,以评估脱色速率和程度以及任何潜在的毒性作用。总体而言,在初始染料浓度为300 mg/L(以RB 19当量表示)且添加30 g/L NaCl的情况下,用RB 19(一种蒽醌染料)或废染料浴修正的培养物中观察到了较高的脱色速率和程度(分别>10 mg/[L·h]和88%)。在RB 19和废染料浴修正的培养物中均观察到了产酸作用的抑制,并且在更大程度上观察到了产甲烷作用的抑制,导致挥发性脂肪酸积累。初始浓度为300 mg/L的RB 21(一种酞菁染料)和RR 198(一种偶氮染料)对混合产甲烷培养物没有产生任何显著抑制作用。基于在添加和不添加NaCl的情况下用RB 19修正的培养物以及添加30 g/L NaCl的对照培养物所获得的结果,盐的抑制作用小于RB 19或染料浴。因此,废染料浴的毒性作用至少部分归因于其主要染料成分RB 19和NaCl。在不存在NaCl的情况下对RB 19脱色产物对产甲烷活性的影响进行的进一步测试表明,这些产物的抑制作用远小于母体染料。尽管在培养受到严重抑制的情况下仍发生了脱色,但在重复的闭环系统中使用产甲烷培养物对全强度活性废染料浴进行生物脱色被认为是不可行的。因此,开发了一种发酵性和耐盐培养物,并在我们实验室成功用于对含有100 g/L NaCl的工业活性染料浴进行脱色。