蛋白质在城市污水活性污泥处理系统中的降解动力学模型研究

研究了蛋白质在厌氧-缺氧-好氧城市污水处理系统中吸附和降解的特性,分别确定了蛋白质在厌氧、缺氧和好氧条件下的吸附等温线模型,建立了蛋白质在厌氧、缺氧和好氧状态下的降解动力学模型,并对模型预测结果进行了验证分析,结果表明,Freundlich模型可以较好地描述蛋白质在厌氧、缺氧和好氧污泥卜的吸附过程,牛血清白蛋白水解成氨基酸是其生物降解过程的控速步骤,序批式动力学降解试验还表明,厌氧降解速率系数K厌、缺氧降解速率系数k缺与好氧降解速率常数的比值分别为0.40和0.98,说明在同一活性污泥系统的厌氧和缺氧条件下,蛋白质也能被较好地降解,模型得到的各池混合液出水中蛋白质的浓度模拟结果与实测结果相一致(相对误差＜10%).无论在厌氧、缺氧还是好氧环境中,酸溶蛋白质没有积累.     

氟苯酚好氧生物降解性能及其与化学结构的相关性研究

利用OxiTopBOD测试仪测定微生物耗氧量的方法,对邻氟苯酚、间氟苯酚和对氟苯酚的好氧生物降解性能进行了研究,结果表明:邻氟苯酚、间氟苯酚和对氟苯酚的耗氧生物降解速率常数分别是0.0093L·g-1·h-1,0.0133L·g-1·h-1和0.0145L·g-1·h-1.降解活性与化学结构的相关性分析表明:辛醇/水分配系数和分子连接指数是影响受试物好氧生物降解性能的两个重要因素.     

糖类在城市污水生物处理系统中的去除机理

研究了厌氧、缺氧和好氧状态下淀粉在城市污水生物处理系统中水相和泥相中吸附和降解的动力学参数,建立了淀粉在厌氧、缺氧、好氧状态下的降解动力学模型,并对模型预测的结果进行了验证.结果表明,Fritz-Schlunder模型可以较好地描述糖类在厌氧、缺氧和好氧污泥上的吸附过程,吸附的大分子糖类迅速水解为低一级的高分子物质和小分子物质;厌氧降解速率系数K厌、缺氧的降解速率系数K缺与好氧的降解速率常数的比值分别为0.40和0.64;所建立的动力学模型能较好的预测出水糖类的浓度(相对误差<10%).     

辛基酚聚氧乙烯醚好氧生物降解产物的GC-MS测定

从上海闵行区污水处理厂曝气池中的污泥和上海孙桥农业园区农田表层土壤样品中分离得到两株好氧降解菌株：B16-2（曝气池）和N1（农田）,都能够不同程度地降解辛基酚聚氧乙烯醚（OPEOn）.利用气相色谱-质谱联用仪对其好氧生物降解产物进行了表征和鉴别.结果表明,两株菌对OPEOn的好氧生物降解都产生了环境雌激素活性物质--辛基酚,从曝气池中分离出的B16-2好氧降解产生了丁基酚聚氧乙烯醚,从仙人掌土壤分离出的N1菌株降解以羟基端EO链的逐渐断裂为主要途径.     

含硫芳香族化合物的好氧微生物降解

本文测定了一批苯硫基（亚砜基、砚基）乙酸酯类化合物的好氧微生物降解速率常数Ｋｂ，在此基础上，对这类化合物的结构与其生物降解速率之间的关系进行了分析，研究表明：苯硫基乙酸酯类化合物的降解速率大于苯磺基乙酸酯类化合物，关两类化合物的降解速率又叁于苯亚砚基乙酸酯类化合物；甲酯比异丙酯易降解；苯环上硝基与氯取代基均会降低化合物的可生化性，且对位硝基对阻碍作用高于邻位取代的硝基；另外，降解速率常数取代基数目     

农村蔬菜废物高温好氧降解协同性及动力学

对太湖流域农村典型蔬菜废物进行了高温好氧降解试验,结果表明,好氧降解d14末有机物降解率大小顺序为:叶菜皮>竹笋壳>叶菜皮 竹笋壳>叶菜皮 茭白壳>茭白壳.对于混合物料,叶菜皮 竹笋壳组有机物降解后期(6~14d)存在非协同降解关系,其主要是由于其难降解组分后期降解存在抑制导致而成;叶菜皮 茭白壳则呈独立降解关系.蔬菜废物高温好氧降解符合一级动力学,降解速率常数在0.036~0.100d-1之间,各不同组物料降解速率大小顺序为:叶菜皮>笋壳>叶菜皮 竹笋壳>叶菜皮 茭白壳>茭白壳.统计分析表明,降解速率与物料纤维素初始浓度相关性最好,指数模型拟和效果最优,可作为蔬菜废物高温好氧降解速率常数的经验公式.图3表6参16     

乙烯基聚合物的好氧生物降解特性

在好氧活性污泥系统生物处理乙烯基聚合物,采用COD30法,并结合TOC、生化呼吸曲线、扫描电子显微镜-能谱(SEM-EDS)、傅里叶红外光谱(FT-IR)及粒径分布研究了乙烯基聚合物的好氧生物降解特性.结果表明,经过30 d的微生物作用,初始COD浓度为100、300、500 mg·L-1的乙烯基聚合物的生物降解去除率分别为37.1%、33.4%、31.1%,乙烯基聚合物的生物降解去除率随初始浓度的增大而减小.降解动力学基本符合一级速率方程,速率常数受初始浓度影响较小.TOC、生化呼吸曲线、SEM-EDS、FT-IR及粒径变化结果进一步表明,乙烯基聚合物在好氧微生物的作用下发生了一定程度的生物降解.FT-IR结果表明乙烯基聚合物的主体结构未发生显著变化,主链上碳元素被矿化的较少.     

取代苯甲酸在江水中的生物降解性及QSBR研究

以松花江水作为微生物源，采用摇瓶法研究了取代苯甲酸的生物降解动力学。高效液相色谱测定了取代苯甲酸浓度随时间变化曲线，得到一级生物降解动力学常数K和降解半衰期t1/2。取代基对降解速度的影响依次为：硝基＞氯代＞氨基；对于同一种取代基，邻位＞对位≈间位。逐步回归分析表明，表征位阻效应的参数MW与表征电性效应的参数pKa相结合，能够较好地拟合取代苯甲酸的生物降解速率常数。同时考察了pH变化对苯甲酸生物降解的影响。     

硝基苯在江水中生物降解动力学模拟研究

以第二松花江哨口断面江水为微生物源,对硝基苯的生物降解动力学进行研究。结果表明,硝基苯在江水中的生物降解过程可由对数方程S=S_0+X_0(1—e~(μmt))描述;丙酮作标准液溶剂时,硝基苯的生物降解速率符合一级动力学方程;由此得到硝基苯生物降解动力学参数,即微生物最大比增长速率μm和一级速率常数K。硝基苯的初始浓度(53.5—535μg/L)对l'm没有明显的影响,温度、驯化条件对μm的影响显著,硝基芳烃、氯苯类化合物对硝基苯的降解有抑制作用。     

活性艳红X-3B的厌氧生物降解与机理

以活性艳红X-3B(RBR)为研究对象,分3个不同浓度组研究其在厌氧颗粒污泥作用下的降解性能,并采用生物降解动力学方程拟合其降解过程,同时利用GC-MS分析RBR的生物降解途径.试验结果表明,RBR在厌氧颗粒污泥中降解性能很好,去除率可达93.67%,且其降解过程符合二级反应动力学,其半衰期约为3.561 h.从GC-MS和UV-可见光谱的分析得出,RBR在厌氧颗粒污泥的作用下偶氮键断裂,且生成的芳香胺类化合物进一步降解为小分子的烃类、酚类、醇类和脂类化合物.     

Occurrence and migration of microplastics and plasticizers in different wastewater and sludge treatment units in municipal wastewater treatment plant

● Reduce the quantifying MPs time by using Nile red staining. ● The removal rate of MPs and PAEs in wastewater and sludge were investigated. ● MPs and PAEs were firstly analyzed during thermal hydrolysis treatment. ● The removal of PAEs from wastewater and sludge was mainly biodegradation. Microplastics (MPs) and plasticizers, such as phthalate esters (PAEs), were frequently detected in municipal wastewater treatment plants (MWTP). Previous research mainly studied the removal of MPs and PAEs in wastewater. However, the occurrence of MPs and PAEs in the sludge was generally ignored. To comprehensively investigate the occurrence and the migration behaviors of MPs and PAEs in MWTP, a series of representative parameters including the number, size, color, shape of MPs, and the concentrations of PAEs in wastewater and sludge were systematically investigated. In this study, the concentrations of MPs in the influent and effluent were 15.46±0.37 and 0.30±0.14 particles/L. The MP removal efficiency of 98.1% was achieved and about 73.8% of MPs were accumulated in the sludge in the MWTP. The numbers of MPs in the sludge before and after digestion were 4.40±0.14 and 0.31±0.01 particles/g (dry sludge), respectively. Fourier Transform Infrared Spectroscopy (ATR FT-IR) analysis showed that the main types of MPs were polyethylene terephthalate (PET), polypropylene (PP), polyethylene (PE), and polystyrene (PS). Six PAEs, including phthalate (DMP), diethyl phthalate (DEP), diisobutyl phthalate (DIBP), ortho dibutyl phthalate (DBP), butyl benzyl phthalate (BBP), and bis(2-ethyl) hexyl phthalate (DEHP), were detected in the MWTP. The concentrations of total PAEs (ΣPAEs) in the influent and effluent were 76.66 and 6.28 µg/L, respectively. The concentrations of ΣPAEs in the sludge before and after digestion were 152.64 and 31.70 µg/g, respectively. In the process of thermal hydrolysis, the number and size of MPs decreased accompanied by the increase of the plasticizer concentration.     

Abiotic association of phthalic acid esters with humic acid of a sludge landfill

The abiotic association between phthalic acid esters (PAEs) and humic substances (HS) in sludge landfill plays an important role in the fate and stability of PAEs. An equilibrium dialysis combined with ¹⁴C-labeling was used to study the abiotic association of two abundant PAEs (diethyl phthalate and di-n-butyl phthalate) with humic acid (HA) isolated from a sludge landfill with different stabilization times and different molecular weights. Elemental analysis and Fourier Transform Infrared Spectrophotometer (FTIR) suggested that high K _A value of HA was related to the high aromatic content and large molecular weight of HA. The results indicated that the association strength of PAEs with HA depended on both the properties of the PAEs and the characteristics of HA. The K _A values of the association were strongly dependent on solution pH, and decreased dramatically as the pH was increased from 3.0 to 9.0. The results suggested that nonspecific hydrophobic interaction between PAEs and HA was the main contributor to the association of the PAEs with HA. The interactive hydrogen-bonds between the HA and the PAEs molecules may also be involved in the association.     

邻苯二甲酸酯的环境污染和生态行为及毒理效应研究进展

邻苯二甲酸酯作为产品改性剂被广泛应用于食品包装、建筑板材、医疗器械等产品中,由于PAEs与塑料分子难以形成强力的共价结合,造成其不断泄露至脂溶性环境中,在基质接触和食物网传递作用下,PAEs被各种生物体蓄积并表现出一定的内分泌干扰效应。文章以PAEs的物化性质及其在大气、水体、土壤中的污染现状为研究基础,介绍了PAEs的生物体蓄积水平与代谢路径,并分别从水解、光解及生物降解3个角度展示了PAEs的环境降解过程与机理;此外,结合实验室报道及社会调查,深入探讨了PAEs的环境激素效应,"致癌、致畸、致突变"效应,酶与激素毒性;最后,基于当前PAEs在毒理分析、降解途径及环境暴露统计研究上的不足,指出需进一步进行复杂食物链毒性积累与放大研究,发展PAEs的生物治理与削减技术以及进行PAEs环境暴露水平调查,确定全面合理的环境标准限值。     

邻苯二甲酸酯类对水生食物链的影响研究进展

邻苯二甲酸酯类(PAEs)增塑剂被普遍用于塑料制品中,在大气、水等环境中广泛存在,其潜在危害受到关注。水环境中的PAEs,从藻类等初级生产者吸收,到浮游动物、游泳动物等通过鳃和皮肤直接接触或捕食摄取,在水生生物之间转化和传递。笔者总结了PAEs在水生食物链中不同营养级生物体的含量,分析了PAEs在食物链中富集和转化的影响因素(辛醇-水分配系数Kow、代谢转化、生长阶段等)。目前的研究表明PAEs可能在食物链中传递,最终在较高营养级生物体中富集。同时总结了5种PAEs(邻苯二甲酸二丁酯、邻苯二甲酸二乙酯、邻苯二甲酯丁苄酯、邻苯二甲酸二(2-乙基)己酯和邻苯二甲酸二甲酯)对水生生物的毒性效应的研究进展,已有研究表明PAEs对藻类的细胞器和抗氧化体系,对鱼类的生殖系统、内分泌系统和抗氧化体系都有一定程度损伤。PAEs在食物链中传递和富集现象的存在会对高营养级水生生物产生潜在危害。针对目前PAEs在食物链中传递的研究数量较少、结构简单等问题,对未来研究方向做了简要分析和展望。     

Investigating into composition,distribution, sources and health risk of phthalic acid esters in street dust of Xi’an City,Northwest China

Phthalic acid esters (PAEs) are widely used as plasticizers and in consumer products, which may enter the environment and present risks to human health. U.S. EPA classifies six PAEs as priority pollutants, which could be accumulated in street dust at the interface of atmosphere, biosphere and geosphere. This study collected a total of 58 street dust samples from Xi’an City in Northwest China and analyzed for concentrations of the priority PAEs. Composition, distribution, sources and health risk of the PAEs were further examined. All the priority PAEs were detected in the street dust. The concentrations of individual PAEs varied between not detected and 183.19 mg/kg. The sum of the 6 priority PAEs (∑6PAEs) ranged from 0.87 to 250.30 mg/kg with a mean of 40.48 mg/kg. The most abundant PAEs in the street dust were di-n-butyl phthalate and di (2-ethylhexyl) phthalate (DEHP). Higher concentrations of ∑6PAEs in the street dust were found in the south and west parts of Xi’an City as well as its urban center, which were possibly attributed to the prevailing northerly Asian winter monsoon. The PAEs in the street dust originated mainly from wide application of plasticizers as well as cosmetics and personal care products. The main pathways of human exposure to PAEs in the street dust were ingestion and dermal adsorption of dust particles. The non-cancer risk of human exposure to PAEs in the street dust was relatively low, while the risk to children was higher than that to adults. The cancer risk of human exposure to DEHP in the street dust was lower than the standard limit value of 10^?6.     

南京市大气气溶胶中酞酸酯的分布特征

利用分级采样器采样 ,高效液相色谱检测 ,研究了南京市春夏秋冬四季六大功能区 (工业区 ,交通区 ,文化区 ,商业区 ,园林风景区和居民生活区 )大气气溶胶中的酞酸酯 .结果表明 :南京市大气气溶胶中检出的酞酸酯有 :邻苯二甲酸二甲酯 (DMP)、邻苯二甲酸二丁酯 (DBP)和邻苯二甲酸二辛酯 (DEHP) ,其含量随功能区和季节而变化 ,平均浓度具有工业区 >居民区 >交通区 >商业区 >文化区 >园林风景区和秋、冬季浓度高于春、夏季的分布特征     

Phthalate esters contamination in soil and plants on agricultural land near an electronic waste recycling site

The accumulation of phthalic acid esters (PAEs) in soil and plants in agricultural land near an electronic waste recycling site in east China has become a great threat to the neighboring environmental quality and human health. Soil and plant samples collected from land under different utilization, including fallow plots, vegetable plots, plots with alfalfa (Medicago sativa L.) as green manure, fallow plots under long-term flooding and fallow plots under alternating wet and dry periods, together with plant samples from relative plots were analyzed for six PAE compounds nominated as prior pollutants by USEPA. In the determined samples, the concentrations of six target PAE pollutants ranged from 0.31–2.39 mg/kg in soil to 1.81–5.77 mg/kg in various plants (dry weight/DW), and their bioconcentration factors (BCFs) ranged from 5.8 to 17.9. Health risk assessments were conducted on target PAEs, known as typical environmental estrogen analogs, based on their accumulation in the edible parts of vegetables. Preliminary risk assessment to human health from soil and daily vegetable intake indicated that DEHP may present a high-exposure risk on all ages of the population in the area by soil ingestion or vegetable consumption. The potential damage that the target PAE compounds may pose to human health should be taken into account in further comprehensive risk assessments in e-waste recycling sites areas. Moreover, alfalfa removed substantial amounts of PAEs from the soil, and its use can be considered a good strategy for in situ remediation of PAEs.     

环境内分泌干扰物——邻苯二甲酸酯的生物降解研究进展

邻苯二甲酸酯是一类重要的合成有机物.主要用作增塑剂来提高塑料树脂的机械性能尤其是柔韧性.近年来,由于在全球范同内的广泛使用,在环境中的普遍存在,以及其内分泌干扰毒性,邻苯二甲酸酯受到了人们越来越多的关注.微生物降解被认为是邻苯二甲酸酯完全矿化的主要途径.邻苯二甲酸酯的降解机制与途径已经在细菌中得到广泛的研究,但是在真菌领域的报道还很少见.本文主要概述了邻苯二甲酸酯的环境污染现状,介绍了其对人和动物的健康危害,并且综述了邻苯二甲酸酯微生物降解的研究进展,包括降解菌的种类、降解的代谢途径及相应的分子机制,以及真菌对邻苯二甲酸酯的降解研究等.     

高级催化氧化法去除水中邻苯二甲酸酯的研究进展

普遍认为,邻苯二甲酸酯类物质（Phthalic Acid Esters,PAEs）是内分泌干扰物质（Endocrine Disrupting Chemicals,EDCs）,被广泛应用于增塑剂、化妆品中,具有致畸性,致癌性,致突变性以及拟/抗雌激素活性、拟/抗甲状腺激素活性等内分泌干扰特性。邻苯二甲酸酯类物质很容易扩散到环境中,在土壤、大气、水环境中均有检出,是环境中常见污染物,严重威胁人体健康和生态环境,已经引起国内外的广泛关注。在综述邻苯二甲酸酯类物质的物理化学性质、毒性影响、国内外天然水体、地下水和生活污水中的污染现状的基础上,讨论消除水环境中PAEs污染的强化混凝、吸附、膜处理、生物处理和高级氧化技术。高级氧化技术因其能够快速有效地去除饮用水和污水中不同种类的有机污染物而备受关注,且发展迅速。重点介绍了高级催化氧化法对水环境中PAEs的去除,包括催化湿式过氧化物氧化过程,催化臭氧氧化过程,光催化氧化过程,超声波、微波辅助催化氧化过程以及高级纳米催化氧化过程。其中,Fenton催化氧化技术在氧化过程中通过使用催化剂或协同紫外光等方式产生高度反应性羟基自由基,可无选择性地将PAEs完全降解为无毒无害的小分子物质,对PAEs的氧化去除效果最好。虽然在高级氧化过程中应用催化剂可大大提高氧化效率和降解程度,但催化氧化法耗能较大、催化剂消耗量大、受水体pH值的影响,且研究大多限于实验室阶段,未能大量投入工业应用,需要进一步发展创新。因此,开发新型高效催化剂、提高催化剂选择性、优化催化氧化反应条件、优化设计催化反应器、与其他技术耦合是水体中PAEs类环境激素污染控制技术的发展方向。     

A new procedure combining GC-MS with accelerated solvent extraction for the analysis of phthalic acid esters in contaminated soils

An optimized procedure based on gas chromatography-mass spectrometry (GC-MS) combined with accelerated solvent extraction (ASE) is developed for the analysis of six phthalic acid esters (PAEs), which are priority soil pollutants nominated by United States Environmental Protection Agency (USEPA). Quantification of PAEs in soil employs ultrasonic extraction (UE) (USEPA 3550) and ASE (USEPA 3545), followed by clean up procedures involving three different chromatography columns and two combined elution methods. GC-MS conditions under selected ion monitoring (SIM) mode are described and quality assurance and quality control (QA/QC) criteria with high accuracy and sensitivity for target analytes were achieved. Method reliability is assured with the use of an isotopically labeled PAE, di-n-butyl phthalate-d4 (DnBP-D4), as a surrogate, and benzyl benzoate (BB) as an internal standard, and with the analysis of certified reference materials (CRM). QA/QC for the developed procedure was tested in four PAE-spiked soils and one PAE-contaminated soil. The four spiked soils were originated from typical Chinese agricultural fields and the contaminated soil was obtained from an electronic waste dismantling area. Instrument detection limits (IDLs) for the six PAEs ranged 0.10–0.31 μg·L^-1 and method detection limits (MDLs) of the four spiked soils varied from a range of 20–70 μg·kg^-1 to a range of 90– 290 μg·kg^-1. Linearity of response between 20 μg·L^-1 and 2 mg·L^-1 was also established and the correlation coefficients (R) were all>0.998. Spiked soil matrix showed relative recovery rates between 75 and 120% for the six target compounds and about 93% for the surrogate substance. The developed procedure is anticipated to be highly applicable for field surveys of soil PAE pollution in China.