造纸中段废水与生活污水合并深度处理工艺

采用水解酸化 CAST 混凝 复合滤池与水解酸化 接触氧化 混凝 复合滤池2种组合工艺对造纸中段废水与生活污水进行合并处理对照试验.结果表明,两种工艺都是切实可行的,二级出水均可达到<污水综合排放标准>(GB8978-1996)二级标准,深度处理出水可达中水水质要求.其中以水解酸化 CAST 混凝 复合滤池组合工艺效果最好.     

印染废水处理过程中污染物及毒性分析

应用水解酸化-A/O(生物活性炭法(PACT))-混凝沉淀组合工艺处理印染废水,深入研究该组合工艺各反应段对印染废水污染物的处理情况,分别用电感耦合等离子光谱(AES/ICP)、气相色谱/质谱联用(GC/MS)以及发光细菌法对各反应段出水所含金属元素、有机物以及毒性进行检测.结果表明,水解酸化-A/O(PACT)-混凝沉淀组合工艺可以有效降解印染废水所含污染物,降低其毒性.     

低能耗印染废水处理工艺与运行条件

采用UASB反应器+三段好氧+混凝沉淀组合工艺处理印染工业园废水。结果表明,工程运行中,通过导流墙的设置,UASB水解酸化反应器的运行以及运行工况的控制,在出水稳定在《城镇污水处理厂污染物排放标准》(GB18918—2002)一级A标准时,该系统处理每吨污水电费为0.36元。     

生物法/人工湿地工艺处理采油废水及其生态毒性削减研究

采用2种生物法/人工湿地工艺(水解酸化/好氧/人工湿地工艺和水解酸化/人工湿地(进水区强化曝气)工艺)处理胜利油田某联合处理站经隔油、混凝处理的采油废水,并运用发光细菌技术研究采油废水在处理过程中的生态毒性削减规律.研究结果表明,在水解酸化段水力停留时间(HRT)为20 h,好氧段HRT为10 h,人工湿地HRT为2 d的工况下,水解酸化/好氧/人工湿地工艺与水解酸化/人工湿地(进水区强化曝气)工艺的出水水质均能满足COD≤80 mg/L、NH_4~+-N≤15 mg/L的处理要求.发光细菌法试验结果表明,经隔油、混凝处理后的采油废水属高毒性废水,再经水解酸化/人工湿地(进水区强化曝气)工艺处理后生态毒性大幅削减,出水生态毒性降至低毒.     

AOAB工艺处理难降解混合化工污水的挂膜启动

采用AOAB(水解酸化A1+生物接触氧化O+深度水解酸化A2+曝气生物滤池BAF)工艺处理难降解混合化工污水,重点研究工艺挂膜方式和生物膜的驯化。结果表明,采用分段连续式挂膜法进行反应器挂膜,20 d即可完成快速挂膜启动;采用分阶段同步培养驯化法驯化生物膜,30 d内可完成高浓度多组分混合化工污水进水的驯化,最终进水COD 1 456 mg/L,出水COD 324 mg/L,总去除率76.85%,驯化效果显著;整个工艺对COD的降解主要集中在生物接触氧化池和曝气生物滤池,驯化期间生物接触氧化池去除率稳定在40%左右,曝气生物滤池去除率稳定在50%以上。同时,通过对比一段水解酸化和深度水解酸化的VFA(挥发性脂肪酸)产出,表明在高有机负荷进水时,一段水解酸化降解大分子有机物的能力有限,但这些有机物可通过二段水解酸化再次降解,由此体现了AOAB工艺在处理多组分混合型的难降解化工污水的优势。     

低污泥产量印染废水处理工艺与运行条件

采用UASB反应器+三段好氧+混凝沉淀组合工艺处理印染工业园废水,对污泥减量化进行探索。结果表明,工程运行中,通过控制运行参数、以及运用UASB水解酸化反应器及生物捕食技术,在出水稳定在《城镇污水处理厂污染物排放标准》(GB18918-2002)一级A标准时,该系统处理每吨污水污泥产量为1 046 g。     

硫酸卷曲霉素生产废水生化前预处理试验研究

对某厂硫酸卷曲霉素废水进行预处理试验,为水处理工程设计提供参考.选择混凝-气浮-水解酸化工艺组合作为预处理工艺,试验表明,依某厂硫酸卷曲霉素生产废水特征,以PAC为混凝剂、PAM为助凝剂,投药量分别为100和5 mg/L条件下,混凝-气浮单元的COD、BOD5和SS去除率分别在42.6%～48.7%、25.5%～40.8%和84.6%～92.6%之间;在水解酸化单元接种厌氧污泥,可以大大缩短污泥驯化时间,用经过14 d驯化时间的污泥处理气浮单元出水,HRT为16 h时,该单元的COD、BOD5去除率分别在8.4%～33.8%和5.0%～19.5%之间;气浮单元、水解酸化单元均提高了出水的可生化性.将混凝-气浮单元与水解酸化单元联合作为硫酸卷曲霉素生产废水的生化处理的前处理措施是可行的.     

混凝-折流式反应器对垃圾渗滤液处理的试验研究

采用混凝、三组水解池和好氧生物滤池串连组成的折流式反应器(BR)联合工艺,对处理芜湖市南郊垃圾填埋场产生的渗滤液进行了试验研究,确定了混凝剂的最佳投加量、最佳碱化脱氮pH等工艺参数.试验结果表明,经过水解反应器(HUSB)反复对垃圾渗滤液进行水解酸化后,能逐步提高废水的BOD5/COD(B/C)(约0.2～0.4),大大提高了好氧生物滤池的COD容积负荷,出水COD平均《400 mg/L,NH3-N平均《30 mg/L.     

混凝—水解酸化—好氧工艺处理印染废水的设计与运行

采用混凝-水解酸化-好氧工艺处理印染废水,设计规模3000m3/d.当进水C0D在571～1752 mg/L时,处理后的出水可达国家<污水综合排放标准>(GB 8978-1996),主要污染物ρ(C0D)＜100mg/L.     

混凝-水解酸化-好氧-混凝工艺处理印染废水

采用“混凝-水解酸化-好氧-混凝”工艺处理印染废水,当进水COD为800—1200mg／L时,出水可达到国家《污水综合排放标准》（GB1978--1996）,其中COD指标甚至达到江苏地方标准《太湖地区城镇污水处理厂及重点工业行业主要水污染物排放限值》（DB32／T1072--2007）。     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.     

Biochemical interaction of six op delayed neurotoxicants with several neurotargets

Abstract

Five organophosphorous insecticides: Leptophos, EPN, Cyano‐fenphos, trichloronate and salithion proved to cause irreversible ataxia not only to chicken but also to mice and sheep. TOCP was included as a reference. Cyanofenphos blocked the catecholamine B‐receptor binding activity with ³H‐norepinephrine at a level similar to that of the specific inhibitor propranolol in the mouse heart preparation. In the lamb heart preparation, the B‐receptor was more sensitive to Leptophos, salithion and TOCP than to propranolol. The six compounds and their oxons were screened for their in‐vitro inhibition to monamine oxidase (MAO), acetyl cholinesterase (AChE) and neurotoxic esterase (NTE) in the brain of either mouse, lamb or chicken. It is believed that their AChE inhibition stands for their acute toxicity, while NTE inhibition is responsible for their paralytic ataxia.     

土壤中砷的化学平衡

本文比较详细地综述了砷的化学特性,环境背景值及来源和循环,土壤中砷的三大化学平衡即沉淀溶解平衡,氧化还原平衡,吸附解吸平衡,以及微生物对砷的转化。     

Elemental uptake by edible herbs and lettuce (Latuca sativa)

The total concentration of toxic elements (aluminum, cadmium, chromium and lead) and selected macro and micro elements (iron, manganese, copper and zinc) are reported in six leafy edible vegetation species, namely lettuce, spinach, cabbage, chards and green and red types of Amaranth herbs. Although spinach and chards had greater than 125 mv of iron, both the amaranthus herbs recorded > than 320 μ g g^{? 1} dry weight. In both the spinach and chard species, the Mn and Zn levels were appreciable recording > 225 μ g g^{? 1} and 150 μ g g^{? 1} dry weight, respectively. Aluminum concentrations were (in μ g g^{? 1} dry weight) lettuce (10), cabbage (11), spinach (167), chards (65), amaranthus green (293) and amaranthus red (233). All the micro and macro elements and the toxic elements (Ni, Cr, Cd and Pb) elements analyzed, were below the recommended maximum permitted levels (RMI) in vegetables. Further the elemental uptake and distribution of the nine elements, at three growth stages of the lettuce plant grown on soil bed under controlled conditions are detailed. In the soil, except for iron (16%), greater than 33% of the other cations were in exchangeable form. Generally in the lettuce plant, roots retained much of the iron (> 224 μ g g^{? 1}) and aluminum (> 360 μ g g^{? 1}), while leaves had less than 200 μ g g^{? 1} of iron and 165 μ g g^{? 1} of Al. Although the concentrations of elements marginally decreased with growth, the lettuce leaves had significant amounts of Mn (30 μ g g^{? 1}), Zn (50 μ g g^{? 1}) and Cu (3.6 μ g g^{? 1}). Some presence of lead in leaves (2.0 μ g g^{? 1}) was noticed, but all the toxic and other elements analyzed were well below the RMI values for the vegetables.     

The dissipation of nonlyphenol in stream and pond water under simulated field conditions

Abstract

The dissipation of 1.0 ppm nonylphenol in stream and pond water, incubated in flasks at 16°C under simulated field conditions up to 44 days indicated that the half‐life was 2.5 days if the flasks were open, and 16 days if they were closed. A transformed product was detected in the closed flasks.

Translocation of nonylphenol in water occurred when treated water samples were incubated in the presence of sediment. After 10 days, nonylphenol was detected only in the sediment, but not in water (detection limit = 10 ppb). About 80% of the nonylphenol was degraded in 71 days, but no degradation occurred if the water and the sediment were autoclaved prior to incubation.