气浮-A/O-SBR法处理肉类集中加工综合废水

南方某城镇集中了较大规模的肉类农产品加工企业。这些企业排放废水量大,有机物浓度高。该城镇采用经企业预处理后集中处理方式,以降低运行成本。采用A/O-SBR的二级强化生物处理工艺,经近2年的运行表明:COD、BOD、动植物油类及悬浮物的去除率高,出水达到GB13457-92《肉类加工工业污染物排放标准》,为当地肉类联合加工企业废水治理解决了一大难题。     

多溴联苯醚胁迫下鲫鱼肝脏微粒体CYP3A1和GST的响应

以鲫鱼Carassius auratus Linn.为试验鱼类,研究了其暴露于不同质量浓度的2,2',4,4'-四溴联苯醚(PBDE-47)和十溴联苯醚(PBDE-209)后鱼肝微粒体中CYP3A1和GST酶活性的动态变化.结果表明,鲫鱼在0.10～5.00 mg·L-1的PBDE-47和5.00～50.0 mg·L-1的PBDE-209中暴露15 d后,除0.10 mg·L-1PBDE-47、5.00 mg·L-1和10.0 mg·L-1PBDE-209试验组外,其余各试验组的鱼肝微粒体中CYP3A1被诱导,呈显著的剂量.效应关系.CYP3A1的活性随着作用时间的延续而上升,到试验第15天时达到最高,但上升速率最快的阶段为试验的第0-5天.而GST酶则表现出不同的特点,呈先升高后降低的趋势.经过15 d试验,除0.10 mg·L-1PBDE.47和5.00 mg·L-1PBDE-209以外的各试验组鲫鱼肝脏微粒体中的GST活性仅为对照组的12.74%～85.35%,表明PBDEs已对鱼体肝脏GST产生了较为严重的影响.研究表明,鱼类肝脏微粒体中CYP3A1和GST酶可作为污染生物标志物来评价PBDEs的早期污染毒理效应.     

四溴双酚A对赤子爱胜蚓的急性毒性及抗氧化防御系统酶的影响

以赤子爱胜蚓(Eisenia fetida)为研究对象,根据OECD指南中的滤纸接触法和人工土壤法研究了四溴双酚A(TBBPA)的急性毒性和对蚯蚓体内抗氧化防御系统酶的影响.结果表明,滤纸接触法和人工土壤法检测TBBPA对蚯蚓的半致死浓度LC50分别为4.90mg·L-(148h)和16.7mg·kg-(114d),TBBPA对蚯蚓具有低等毒性.当TBBPA的浓度在0.05和0.1mg·kg-1时对蚯蚓超氧化物歧化酶(SOD)产生显著诱导;在0.05mg·kg-1时,对过氧化氢酶(CAT)和谷胱甘肽硫转移酶(GST)也产生显著诱导;脂质过氧化产物丙二醛(MDA)随TBBPA浓度的升高逐渐增加,呈良好的剂量效应关系(R2=0.97,p<0.01).SOD、CAT、GST和MDA可以作为土壤生态早期预警中潜在的敏感的生物标志物.     

A2O-BAF反硝化除磷工艺丝状菌膨胀的发生及控制

为了有效控制A2O-BAF反硝化除磷工艺处理实际生活污水时产生的丝状菌污泥膨胀,研究了有机负荷和冬季突然降温对丝状菌污泥膨胀的影响.结果表明:当有机负荷低于0.30kgCOD/(kgMLSS·d)时,系统中存在轻度的丝状菌污泥膨胀现象;当有机负荷高于0.55kgCOD/(kgMLSS·d)时,容易引发严重的丝状菌污泥膨胀,调节有机负荷可使丝状菌污泥膨胀得到有效控制.冬季突然降温也会导致污泥膨胀的发生,恢复温度后,污泥沉降性能恢复正常,丝状菌污泥膨胀亦得到有效控制.     

Ca2+对酸性硫酸盐环境中次生铁矿物合成的影响

通过摇瓶培养试验,在富铁酸性硫酸盐环境中,探析0、50、100、200或400mg/L Ca2+加入对嗜酸性氧化亚铁硫杆菌(A. ferrooxidans)生物合成次生铁矿物过程的影响.分析了体系pH值、氧化还原电位(ORP)、Fe2+氧化率、总Fe沉淀率以及次生铁矿物矿相等相关指标的变化情况.结果表明,0~24h培养过程中,各体系pH值、ORP、Fe2+氧化率及总Fe沉淀率变化幅度基本一致.24~108h培养过程中,体系中Ca2+加入量越大,Fe2+氧化越迅速,相应总Fe沉淀率相对较高.400mg/L Ca2+的加入使得体系Fe2+在72h氧化完全,总Fe沉淀率在108h达到39.1%.0、50、100或200mg/L Ca2+ 加入的体系在24~84h培养过程中,体系Fe2+氧化速率随着Ca2+加入量逐渐增加而依次升高,并在84h Fe2+氧化完全,且在108h,相应体系总Fe沉淀率分别为27.0%、29.7%、33.9%或36.9%.不同体系所得次生铁矿物均为施氏矿物与黄铁矾的混合物.本研究结果对明晰富铁酸性硫酸盐环境钙离子调控生物成因次生铁矿物合成的影响机理有一定指导意义.     

Enzyme-linked immunosorbent assay for bisphenol A: Assay optimization and its application for surface water analysis

A range of ELISAs in indirect and direct formats for the determination of bisphenol A (BPA) was developed. Bisphenol A carboxymethyl ether (BPA-CME), (BPA-CPE) and 4,4-bis(4-hydroxyphenyl)valeric acid were coupled with bovine serum albumin (BSA) (immunogens for the production of polyclonal antibodies), ovalbumin (OVA) and horseradish peroxidase. In general, the indirect assay was more sensitive and specific than the direct one. Using heterologous combinations of immunoreagents in the indirect assay allowed to increase assay sensitivity and specificity. The highest sensitivity was obtained for the antibodies produced against a conjugate of BPA-CPE with BSA and a conjugate of 4,4-bis(4-hydroxyphenyl)valeric acid with OVA. The detection limit of BPA in phosphate buffer was 0.03?ng?mL^?1. The assay developed was also the most specific towards BPA. Maximum cross-reactivity values did not exceed 11% for 4-cumylphenol, 5% for bisphenol E and 2% for bisphenol S. Finally, the developed assay was used to analyze surface water samples spiked with known amount of BPA. The assay showed good recovery values (85–109%) for surface water with mineralization level lower than 500?mg?L^?1.     

Endocrine disruptors in the Leça River and nearby Porto Coast (NW Portugal): presence of estrogenic compounds and hypoxic conditions

The Leça River and two beaches close to the north and south margins of the estuary, nowadays an important seaport harbor, show signs of contamination. However, the chemical nature of that contamination is uncertain. Therefore, this study checked for the presence of 11 endocrine disrupting compounds (EDCs) of animal (17β-estradiol and estrone), pharmaceutical (17α-ethynylestradiol), and industrial (alkylphenols, alkylphenol ethoxylates, and bisphenol A) origins in water samples collected from six points at the river gradient and at two sites in the coastline (Atlantic Ocean). Along with the EDCs, evaluated by gas chromatography – mass spectroscopy (GC-MS) during spring, summer, and autumn, physico-chemical parameters were also assessed and particular attention was given to dissolved oxygen (DO) levels. Data showed the presence of high amounts of estrogens (up to 10?ng?L^?1 for estrone) and industrial compounds (up to 2?µg?L^?1 for the nonylphenol ethoxylates) at both river and seacoast. Along with this, clear signs of hypoxia were found in the river (DO??1 at several sampling sites). Taking into account these issues, it was concluded that there are local conditions for the occurrence of endocrine disruption in aquatic animals.     

Characterization and in vitro biological effects of ambient air PM10 from a rural,an industrial and an urban site in Sulaimani City,Iraq

Abstract

High urban atmospheric pollution is caused by economic and industrial growth, especially in developing countries. The objective of this study was to assess possible relationships between in vitro effects on human alveolar epithelial cells of source-related dust types collected at Sulaimani City (Iraq), and to determine their mineralogical and chemical composition. A passive sampler was used to collect dust particles at a rural, an industrial and an urban sampling site during July and August 2014. The samples were size-fractionated by a low-pressure impactor to obtain respirable dust with aerodynamic diameters of less than 10?µm. The dust was mainly composed of quartz and calcite. Chrysotile fibers (white asbestos) were also found at the urban site. Dust from the industrial and urban sites triggered cytotoxic and genotoxic effects in the cells, whereas only minor effects were observed for the sample from the rural site.     

IC+A/O工艺在制药废水处理中的应用

针对某制药公司生产废水的特点,采用高效厌氧反应器——内循环厌氧反应器(简称IC工艺)+A/O工艺进行处理。系统稳定运行后,在进水ρ(COD)为3 500 mg/L、ρ(SS)为300 mg/L时,去除率分别达到97.9%、92.5%。处理后出水水质稳定,达到GB 8978—1996《污水综合排放标准》一级标准。     

Simultaneous removal of arsenate and fluoride from water by AI-Fe （hydr）oxides

A1-Fe （hydr）oxides with different A1/Fe molar ratios （4：1, 1：1, 1：4, 0：1） were prepared using a co- precipitation method and were then employed for simultaneous removal of arsenate and fluoride. The 4A1 ： Fe was superior to other adsorbents for removal of arsenate and fluoride in the pH range of 5.0-9.0. The adsorption capacity of the A1-Fe （hydr）oxides for arsenate and fluoride at pH 6.50.3 increased with increasing A1 content in the adsorbents. The linear relationship between the amount of OH released from the adsorbent and the amount of arsenate or fluoride adsorbent by 4A1 ： Fe indicated that the adsorption of arsenate and fluoride by A1- Fe （hydr）oxides was realized primarily through quantita- tive ligand exchange. Moreover, there was a very good correlation between the surface hydroxyl group densities of A1-Fe （hydr）oxides and their adsorption capacities for arsenate or fluoride. The highest adsorption capacity for arsenate and fluoride by 4A1 ： Fe is mainly ascribed to its highest surface hydroxyl group density besides its largest pHpzc. The dosage of adsorbent necessary to remove arsenate and fluoride to meet the drinking water standard was mainly determined by the presence of fluoride since fluoride was generally present in groundwater at much higher concentration than arsenate.