Biodegradation of methyl red by Bacillus sp. strain UN2: decolorization capacity,metabolites characterization,and enzyme analysis

Azo dyes are recalcitrant and refractory pollutants that constitute a significant menace to the environment. The present study is focused on exploring the capability of Bacillus sp. strain UN2 for application in methyl red (MR) degradation. Effects of physicochemical parameters (pH of medium, temperature, initial concentration of dye, and composition of the medium) were studied in detail. The suitable pH and temperature range for MR degradation by strain UN2 were respectively 7.0–9.0 and 30–40 °C, and the optimal pH value and temperature were respectively 8.0 and 35 °C. Mg²⁺ and Mn²⁺ (1 mM) were found to significantly accelerate the MR removal rate, while the enhancement by either Fe³⁺ or Fe²⁺ was slight. Under the optimal degradation conditions, strain UN2 exhibited greater than 98 % degradation of the toxic azo dye MR (100 ppm) within 30 min. Analysis of samples from decolorized culture flasks confirmed biodegradation of MR into two prime metabolites: N,N′dimethyl-p-phenyle-nediamine and 2-aminobenzoic acid. A study of the enzymes responsible for the biodegradation of MR, in the control and cells obtained during (10 min) and after (30 min) degradation, showed a significant increase in the activities of azoreductase, laccase, and NADH-DCIP reductase. Furthermore, a phytotoxicity analysis demonstrated that the germination inhibition was almost eliminated for both the plants Triticum aestivum and Sorghum bicolor by MR metabolites at 100 mg/L concentration, yet the germination inhibition of parent dye was significant. Consequently, the high efficiency of MR degradation enables this strain to be a potential candidate for bioremediation of wastewater containing MR.     

Effects of di-n-butyl phthalate on the physiology and ultrastructure of cucumber seedling roots

Agricultural pollution caused by the use of plastic sheetings has been documented to be a widespread problem in most of the major crop-planting regions of the world. In order to better understand the phytotoxic mechanisms induced by phthalic acid esters involved with this problem, Cucumber sativus L. cv Jinyan No. 4 were sown in pots to the three-leaf-stage in the presence of di-n-butyl phthalate (DBP; 0, 30, 50, 100, and 200 mg L^?1) for 1, 3, 5, or 7 days. Physiology, biochemistry, and ultrastructure of seedling roots were examined. The results indicated that activities of three antioxidant enzymes (superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD)) were stimulated at low-DBP treatments and decreased under higher levels (>100 mg L^?1) compared to the controls. On the other hand, SOD and POD provided a better defense against DBP-induced oxidative damage in the roots of cucumber seeding, compared to CAT. The productions of both malondialdehyde (MDA) and proline (Pro) were promoted under DBP stress. Visible impact on the cytoderm, mitochondrion, and vacuole was detected, possibly as a consequence of free radical generation. These results suggested that activation of the antioxidant system by DBP led to the formation of reactive oxygen species that resulted in cellular damage.     

Occurrence,distribution, and multi-phase partitioning of triclocarban and triclosan in an urban river receiving wastewater treatment plants effluent in China

Occurrence, distribution, spatial and seasonal variations, and partitioning between aqueous phase and suspended particulate matters (SPM) of triclocarban (TCC) and triclosan (TCS) in Xiaoqing River, which receives wastewater treatment plant (WWTP) effluents, were studied. The distribution of the total TCC and TCS levels in surface water and sediments along the river were discussed. The highest TCC and TCS concentrations were both found near the discharge port of WWTPs, and the TCC and TCS levels decreased downstream of the WWTPs as a result of their distances from the source of WWTP discharges. The mean values of TCC and TCS in low-flow season were 1.62 and 1.80 times, respectively, as much as in high-flow season in surface water. The study on partitioning of TCC and TCS between aqueous phase and SPM shown the mean level of dissolved TCC accounted for about 10 % of the total level in surface water, whereas the TCS level was about 30 %. The TCC concentrations detected in the surface sediment samples (0 to 5 cm) ranged from 226 to 1,956 ng/g, with a mean value of 733 ng/g. The TCS levels were between 85 and 705 ng/g, with a mean value of 255 ng/g. The distribution and variations of TCC and TCS in sediments along the river were highly consistent with those in the water phase. The TCC and TCS levels in deep sediments (5 to 10 cm) were significantly lower than those in surface sediments. The mean TCC level in surface sediments was about 2.4 times as much as in deep sediments, and the TCS level in surface sediments was 3.1 times as much as in deep sediments.     

氧活性粒子氧化NO生成HNO_3

采用强电离介质阻挡放电方法制取高浓度氧活性粒子(O+2、O3)并注入气体外排烟道中,实现O+2、O3氧化NO转化成资源酸(HNO3)的等离子化学反应。描述强电离放电的氧活性粒子产生器,讨论烟道中O+2、O3氧化NO成HNO3等离子体反应机制,分析回收酸液的NO-2、NO-3离子种类及浓度。考察强电离放电等离子体源的输入功率、水体积百分比、气体温度、气体流速对NOx氧化率的影响。氧化率为97.2%的最佳实验条件是:O+2浓度为1.38×1010个/cm3,O3浓度为210 mg/L,烟气温度为65℃,H2O体积浓度为5.6%,停留时间为0.94 s。     

介质阻挡放电协同Ag/Al_2O_3对NO_x脱除的影响

为有效去除发电厂烟气中产生的NOx,利用介质阻挡放电(DBD)产生低温等离子体并结合催化剂Ag/Al2O3进行烟气脱硝实验,研究了在加入乙烯的条件下,平均负载量、催化温度和装置的布置方式对NOx脱除的影响。结果表明,随着负载的增多,NO脱除率呈现先增大后减小的趋势,5种负载量中最佳为1.76%;随着催化温度的升高,NO脱除率同样呈现先增大后减小的趋势,最佳的催化温度为150℃左右;3种不同布置方式对NO和NOx脱除有明显差别,单独催化剂在NO和NOx的脱除率都比较低;单独介质阻挡放电NO脱除率很高,但是NOx很却很低;而两者结合在NO和NOx都达到了很好的效果。     

Role of cosubstrate and bioaccessibility played in the enhanced anaerobic biodegradation of organochlorine pesticides (OCPs) in a paddy soil by nitrate and methyl-β-cyclodextrin amendments

The present study was conducted to investigate the anaerobic biodegradation potential of biostimulation by nitrate (KNO₃) and methyl-β-cyclodextrin (MCD) addition on an aged organochlorine pesticide (OCP)-contaminated paddy soil. After 180 days of incubation, total OCP biodegradation was highest in soil receiving the addition of nitrate and MCD simultaneously and then followed by nitrate addition, MCD addition, and control. The highest biodegradation of chlordanes, hexachlorocyclohexanes, endosulfans, and total OCPs was 74.3, 63.5, 51.2, and 65.1 %, respectively. Meanwhile, MCD addition significantly increased OCP bioaccessibility (p?<?0.05) evaluated by Tenax TA extraction and a three-compartment model method. Moreover, the addition of nitrate and MCD also obtained the highest values of soil microbial activities, including soil microbial biomass carbon and nitrogen, ATP production, denitrifying bacteria count, and nitrate reductase activity. Such similar trend between OCP biodegradation and soil-denitrifying activities suggests a close relationship between OCP biodegradation and N cycling and the indirect/direct involvement of soil microorganisms, especially denitrifying microorganisms in the anaerobic biodegradation of OCPs.     

改性活性炭对水中铬离子(Ⅵ)的吸附性能

为了研究改性前后活性炭对水中铬离子(Ⅵ)的吸附效果,以磷酸活性炭(PAC)为原料,用10%硝酸改性得到硝酸改性活性炭(N-PAC)及直接蒸发法载铁改性得到载铁活性炭(Fe-PAC)。通过静态吸附研究表明,改性后活性炭对Cr(Ⅵ)的吸附率有较大提高。在常温、自然pH条件下,0.2 g活性炭处理50 mL浓度为100 mg/L的含Cr(Ⅵ)溶液,N-PAC和Fe-PAC对Cr(Ⅵ)的吸附率分别为79.21%和90.59%,都高于原PAC对Cr(Ⅵ)的吸附率49.58%。pH从2.2升高到11.92,Fe-PAC对Cr(Ⅵ)的吸附率从99.86%降低到14.77%,N-PAC则从99.86%降低到3.23%,PAC从97.05%降低到2.53%。温度从25℃升高到70℃,3种活性炭对Cr(Ⅵ)吸附率都有较大提高,都增加到98%以上。且吸附过程较符合Langmuir等温吸附模型。     

悬挂链生物接触氧化工艺处理河道污水

采用悬挂链曝气式接触氧化工艺在3个时段内处理城市河道污水,通过采用磷脂法、TTC-脱氢酶活性法和MPN法研究载体表面生物膜特性,来验证装置的水质净化效果。结果表明,进水水质变化幅度较大的时段1内,水质对缺氧区和好氧区内生物膜量及活性有很大冲击,对污染物的去除效果影响不大,COD、NH+4-N、TN和TP的平均去除率分别达到75.9%、80.8%、64.6%和78.3%;进水水质稳定的时段2内,缺氧区和好氧区内生物膜量和活性要高于其他时段,COD、NH+4-N、TN和TP的平均去除率分别达到77.0%、80.6%、69.4%和55.3%;低温运行的时段3内,缺氧区和好氧区内生物膜量和活性都低于其他时段,水质净化效果明显下降,COD、NH+4-N、TN和TP的平均去除率分别为71.1%、68.5%、48.9%和46.6%。     

游泳池中隐孢子虫卵囊替代物的去除

隐孢子虫是常见的球状寄生虫。接触含有隐孢子虫卵囊的水体可致隐孢子虫病,主要的临床表现为腹泻,严重者可致死。游泳池是主要的传播场所。采用容积为5 500 L的游泳池,进行隐孢子虫卵囊替代物的修复模拟实验,研究在游泳池条件下絮凝沙滤技术对直径为4.5μm隐孢子虫卵囊替代物的去除效果。实验结果表明,氯化铝剂量为0.1 mg/L,沙滤料高度为30 cm,内循环流速为11.5 L/min,对隐孢子虫卵囊替代物去除率在90%以上。该技术对浊度具有较好的处理效果,当进水浊度降低且接近于出水浊度时,系统进入稳定运行阶段,对虫卵囊替代物去除率可以达到96%。     

两级EGSB反应器处理焦化废水的实验研究

采用两级膨胀颗粒污泥床(EGSB)反应器在微氧条件下处理焦化废水,分别考察了一级和二级EGSB反应器(EGSBⅠ和EGSBⅡ)对污染物的去除效果。结果表明,系统能够高效去除COD和NH3-N,EGSBⅠ主要用于去除COD,EGSBⅡ主要用于去除NH3-N。总水力停留时间(HRT)为24 h(EGSBⅠ12 h+EGSBⅡ12 h),系统对952 mg/L的COD、41.3 mg/L的NH3-N、34.55 mg/L的挥发酚、295.8 mg/L的硫氰化物和0.89 mg/L的氰化物的平均去除率分别为78.1%、81.3%、100%、98.1%和89.9%。出水COD、NH3-N、挥发酚、硫氰化物和氰化物的平均浓度分别为208、7.7、0、5.7和0.09 mg/L。出水NH3-N、挥发酚和氰化物浓度均低于《炼焦化学工业污染物排放标准》(GB 16171-2012)的直接排放限值。