假单胞菌好氧降解四溴双酚A的特性

为了解四溴双酚A(TBBPA)的好氧降解特性,采用选择富集法从活性污泥中分离出一株能够高效降解四溴双酚A的菌株。根据其形态、生理生化特性及16S rDNA核苷酸序列分析,该菌株被鉴定为假单胞菌属(Pseudomonas sp.)。研究结果表明,该菌株可通过好氧共代谢方式实现四溴双酚A的降解,葡萄糖是四溴双酚A降解的最佳碳源,其最优降解条件为葡萄糖8 g/L,牛肉膏0.5 g/L,pH值为7.0,培养温度为35℃,摇床转速为150 r/min。在该条件下其生物降解过程符合一级动力学模型,6 d后的降解率高达95.6%。LC-MS结果表明,四溴双酚A在好氧降解过程中会生成异丙苯酚类物质。     

抗铬菌株的筛选鉴定及其生物学特性和吸附特性

利用微生物分离纯化技术,在培养基中加入不同浓度的Cr3+、Cr6+,经过长时间驯化,从污染土壤中筛选出2株对Cr具有较高抗性的菌株(A和B),对其进行了形态、生理生化特性及分子生物学鉴定,并研究了其最佳生长条件及对Cr3+的生物吸附规律。结果表明,菌株A和B分别为蜡状芽孢杆菌(Bacillus cereus)和米根霉菌(Rhizopus oryzae)。菌株A和B的最适生长pH值均为7,最适生长温度均为30℃,最佳装液量为80~100 mL(250 mL摇瓶)。在培养时间一定时,随着Cr3+浓度的增加,菌株对Cr3+的吸附率减少,而生物吸附量则逐渐增大;在Cr3+浓度一定时,随着培养时间的延长,菌体对Cr3+的吸附率呈现出先增加后减少的趋势,这与生物吸附量的变化趋势基本一致。在Cr3+浓度为100 mg/L时,菌株A和B对Cr3+的吸附率达到最大,分别为51.47%和46.36%。     

Tree bark as a passive air sampler to indicate atmospheric polybrominated diphenyl ethers (PBDEs) in southeastern China

The different barks were sampled to discuss the influence of the tree species, trunk circumference, and bark thickness on the accumulation processes of polybrominated diphenyl ethers (PBDEs) from air into the bark. The results of different PBDE concentrations indicated that barks with a thickness of 0–3 mm collected from weeping willow, Camphor tree, and Masson pine, the trunk circumferences of which were 100 to 150 cm, were better PBDEs passive samplers. Furthermore, tree bark and the corresponding air samples were collected at Anji (AJ), Hangzhou (HZ), Shanghai (SH), and Wenling (WL) to investigate the relationship between the PBDE concentrations in bark and those in air. In addition, the significant correlation (r ²?=?0.906; P?<?0.05) indicated that atmospheric PBDEs were the principle source for the accumulation of PBDEs in the barks. In this study, the log K _BA (bark–air partition coefficient) of individual PBDE congeners at the four sites were in the range from 5.69 to 6.79. Finally, the total PBDE concentration in WL was 5 to 20 times higher than in the other three cities. The result indicated that crude household workshops contributed a heavy amount of PBDEs pollution to the environment, which had been verified by the spatial distribution of PBDEs levels in barks collected at Wenling (range, 26.53–1317.68 ng/g dw). The good correlation between the PBDE concentrations in the barks and the air samples and the variations of the PBDE concentrations in tree barks collected from different sites reflected that the bark could be used as a passive sampler to indicate the atmospheric PBDEs.     

Concentrations,atmospheric partitioning,and air–water/soil surface exchange of polychlorinated dibenzo-p-dioxin and dibenzofuran along the upper reaches of the Haihe River basin,North China

Polychlorinated dibenzo-p-dioxin and dibenzofuran (PCDD/PCDF) were overall measured and compared in ambient air, water, soils, and sediments along the upper reaches of the Haihe River of North China, so as to evaluate their concentrations, profiles, and to understand the processes of gas–particle partitioning and air–water/soil exchange. The following results were obtained: (1) The average concentrations (toxic equivalents, TEQs) of 2,3,7,8-PCDD/PCDF in air, water, sediment, and soil samples were 4,855 fg/m³, 9.5 pg/L, 99.2 pg/g dry weight (dw), and 56.4 pg/g (203 fg TEQ/m³, 0.46 pg TEQ/L, 2.2 pg TEQ/g dw, and 1.3 pg TEQ/g, respectively), respectively. (2) Although OCDF, 1,2,3,4,6,7,8-HpCDF, OCDD, and 1,2,3,4,6,7,8-HpCDD were the dominant congeners among four environmental sinks, obvious discrepancies of these congener and homologue patterns of PCDD/PCDF were observed still. (3) Significant linear correlations for PCDD/PCDF were observed between the gas–particle partition coefficient (K _p) and the subcooled liquid vapor pressure (P _L ⁰) and octanol–air partition coefficient (K _oa). (4) Fugacity fraction values of air–water exchange indicated that most of PCDD/PCDF homologues were dominated by net volatilization from water into air. The low-chlorinated PCDD/PCDF (tetra- to hexa-) presented a strong net volatilization from the soil into air, while high-chlorinated PCDD/PCDF (hepta- to octa-) were mainly close to equilibrium for air–soil exchange.     

基于改性凹凸棒土的强化混凝处理高藻低浊原水工艺

针对水厂低浊高藻水的处理难题,研究了改性凹凸棒土(改性凹土)联合聚合氯化铝(PAC)强化混凝的除藻除浊效果。设计实验原水条件为叶绿素a(chl-a)浓度为98.58~110.35μg/L,浊度(5.6±0.5)NTU。考察了PAC和改性凹土的复配投加量、混凝沉淀时间、pH、投加顺序、搅拌速率等工艺参数对Chl-a和浊度耦合去除效果的影响。结果表明,"PAC+改性凹土"对Chl-a和浊度的去除效果明显优于单投PAC的效果。当PAC投药量12 mg/L,改性凹土投药量10 mg/L,沉淀时间20 min时,对Chl-a和浊度的去除率可分别达到92.5%和89.2%,可至少减少40%的PAC投量,且形成的矾花密实,沉降速度快,去除效率高。最适pH范围为7~8。投加顺序应为先投加改性凹土,混合搅拌转数宜慢速,可控制为50 r/min。     

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%。     

不同酶强化污泥为燃料微生物燃料电池特性对比分析

采用单室无膜悬浮阴极微生物燃料电池(MFC),对比分析了蛋白酶和淀粉酶强化剩余污泥为燃料的MFC(ESMFC)产电特性、酶特性和污泥减量化效果。研究表明,投加蛋白酶的ESMFC最大功率密度比对照组增加106.2%,投加淀粉酶时ESMFC最大功率密度比对照组增加48%。蛋白酶作用主要体现在投加后的前12小时,而淀粉酶作用时间则较长,为投加后的前144小时,但在运行前期,由于高温作用,导致系统内的酶活性较强,投加的淀粉酶作用则不明显。投加蛋白酶的系统内TCOD、TSS和VSS去除率分别为82%、65%和85%,而投加淀粉酶的系统内TCOD、TSS和VSS去除率分别达到86%、67%和88%。此研究对于ESMFC中外加酶的选择具有一定意义。     

纳米二氧化钛复合石墨烯催化剂的制备及处理染料废水

以硫酸钛为原料,采用共沉淀法,制备了一系列纳米二氧化钛复合石墨烯催化剂,采用XRD和FTIR对样品进行表征。通过紫外光照射亚甲基蓝溶液光催化降解实验,研究石墨烯的加入量对TiO2光催化性能的影响,结果表明,TiO2-GO-5具有最佳的光催化性能。在pH=6.00、TiO2-GO-5的投加量为0.070 g/50 mL、光照3 h条件下,100 mg/L亚甲基蓝溶液的脱色率达到最大值为90.52%。     

负载纳米TiO_2凹凸棒黏土的制备表征及对Mn~(2+)的吸附性能

以溶胶-凝胶法制备了负载纳米TiO2凹凸棒黏土吸附剂,采用SEM、XRD等分析方法对负载纳米TiO2凹凸棒黏土前后的结构进行了表征,并对Mn2+进行了吸附性能的研究。结果表明:经过高温焙烧后的负载纳米TiO2凹凸棒黏土吸附剂较负载前的凹凸棒黏土,因其结构中的结晶水和沸石水脱失,内部孔道面积和表面积增加,活性吸附位点的数量增大,吸附能力有了明显提高。在室温条件下(20~25℃),pH为5~6,吸附平衡时间为120 min时,负载纳米TiO2凹凸棒黏土吸附剂对Mn2+有较好的吸附效果。     

碱液预处理玉米秸秆的条件优化及添加剂的选择

利用稀NaOH溶液预处理玉米秸秆,以去除木质素,减少半纤维素、纤维素的损失为目的,采用响应曲面法对预处理条件进行优化,得到的最佳预处理条件为:NaOH溶液浓度0.77%(w/w),预处理时间16 h,温度45.6℃。并且,进一步研究了不同添加剂(聚乙二醇、吐温-80和尿素)与NaOH溶液协同作用下秸秆中木质素的去除效果,结果表明尿素与NaOH的混合溶液对木质素去除效果最显著。秸秆在45.6℃,0.77%NaOH和0.2%尿素混合溶液中浸泡16 h后,纤维素回收率为86.33%,半纤维素回收率为69.89%,木质素去除率为64.93%;与原秸秆相比,纤维素含量提高了31.70%,半纤维素含量提高了6.62%,木质素含量减少了46.48%。