厌氧折流板反应器处理低浓度废水的运行特性研究

接种厌氧絮状污泥,采用厌氧折流板反应器在中温下进行了处理低浓度废水的试验研究.结果表明,厌氧折流板反应器有效去除了废水中的有机物,平均去除率稳定在80%以上;启动迅速,在35 d内完成,启动性能较EGSB优;水力负荷起着重要的作用;在提高负荷阶段的初期,反应器COD去除率有较大波动,随着负荷的加大,这一现象逐渐消失;在容积负荷小于2.15 kg COD/m3·d时,进水容积负荷与基质去除负荷率之间具有明显的线性正比关系;反应器的前面隔室对有机物的去除起到主要作用;在长期运行的处理低浓度废水的ABR反应器中存在产酸相和产甲烷相的自然分离现象.     

不同好氧预处理方式对餐厨垃圾产甲烷的影响

为了研究不同好氧预处理方式对餐厨垃圾厌氧消化产甲烷的影响,通过建立3个模拟厌氧生物反应器,研究了传统厌氧生物反应器C1、上层好氧预处理-厌氧生物反应器C2和底部好氧预处理-厌氧生物反应器C3 3种不同操作条件下的产甲烷过程.结果表明,挥发性有机酸的累积使C1始终处于产甲烷滞后阶段;而C2、C3的好氧预处理通过加快易水解酸化组分和过量挥发性有机酸的好氧降解,有效缓解了酸性抑制,产甲烷滞后时间明显缩短至10 d内.第32天C2停止上层曝气后,在27 d内甲烷浓度达到了50％以上,同时,产甲烷速率迅速上升,并在第81天可达到峰值773 mL/(kg·d).C3在第11天停止底部曝气后,虽然经过22 d的时间甲烷浓度即上升至50％,但之后产甲烷速率经历回落阶段后再次逐渐上升,在实验结束时仅达到517 mL/(kg·d).上层曝气的好氧预处理方式所需曝气时间相对较长,但其产甲烷启动快,与底部曝气相比,其后期的甲烷化过程更稳定并可达到较高的产甲烷速率.     

牡蛎壳粉末投加UASB反应器的运行特性

采用牡蛎壳粉末作为UASB反应器的辅助介质,探讨了牡蛎壳钙盐的溶出特性,系统考察了运行期中牡蛎壳粉末添加方式、进水有机负荷、水力停留时间等因素对反应器出水COD、碱度与pH的影响,分析了污泥比产甲烷活性变化。结果表明,当初始pH从5到9变化时,牡蛎壳粉末溶出Ca2+浓度为40~65 mg/L,平衡pH稳定在7.7~8.0;当进水COD负荷从3.4 kg/(m3·d)逐渐增至7.0 kg/(m3·d)、牡蛎壳粉末投加量从1.5 g/d逐渐增至3.2 g/d时,与未投加的反应器相比,投加牡蛎壳粉末反应器的启动周期缩短了10%左右,COD去除率与比产甲烷活性分别提高了13.3%和22%。投加牡蛎壳粉末可有效提供碱度,加快污泥的颗粒化进程。     

两相厌氧消化工艺处理鸡粪

以鸡粪为发酵原料,采用序批式两相厌氧消化工艺在中温条件(37℃)下对其进行消化处理。分别将水解酸化相和产甲烷相pH值控制在5.5±0.3和7.0±0.3,通过改变进样含固率(TS)研究有机负荷(OLR)对两相消化系统处理鸡粪过程中污染物转化和去除效果的影响。结果表明,水解酸化相出水总有机碳(TOC)、挥发酸(VFAs)和氨氮(NH4+-N)浓度都随OLR升高而升高。VFAs组成相对稳定,其中乙酸占总VFAs浓度的57%～64%,其次为正丁酸和丙酸。产甲烷相出水TOC和VFAs稳定在较低水平,TOC去除率最大达到90%以上。产甲烷相进水氨氮主要以NH4+形式在反应器内不断积累。实验后期产甲烷相生物气中甲烷体积分数维持在64%上,证明两相消化系统在实验条件下良好运行。     

机械淋滤-厌氧生物组合工艺处理有机生活垃圾中试研究

采用机械淋滤/厌氧生物组合工艺,充分发挥机械淋滤反应器的水解酸化功能和厌氧生物反应器的产甲烷功能,对有机生活垃圾进行了中试规模处理。厌氧生物反应器经过接种,15 d驯化完成。厌氧反应器出水回流淋洗水量对机械淋滤反应器运行特征有较大影响,当回流淋洗水量为3.0 m3/d时,淋滤液COD、VFA第8天时浓度分别为41 000 kg/L和2 000 kg/L。对机械淋滤反应器/厌氧反应器组合工艺进行了多批次实验,每吨有机生活垃圾平均产生沼气87.2 m3,甲烷含量稳定在75%,平均产沼系数为0.46 m3/kg COD,厌氧生物反应器出水COD平均值为560 mg/L,在对有机生活垃圾处理的同时实现有机生活垃圾资源化利用。     

新型化粪池处理生活污水启动阶段的实验

在常温的条件下,用厌氧折流板反应器(ABR)化粪池、YDT填料化粪池和传统三格式化粪池处理生活污水,进行了对照实验研究。实验结果表明,在温度为14～29℃,HRT为36 h时,反应器运行85 d后,对以上3个反应器进出水中CODtot、CODdis、氨氮、总氮、总磷进行测定,在水温24℃稳定阶段,ABR化粪池和YDT填料化粪池CODtot去除率比传统化粪池分别提高30.5%和9.2%;在水温16℃稳定阶段时,该值分别提高10.9%和9.0%。总氮和氨氮去除率在5%～30%之间,稳定运行后总磷去除率为5%左右。通过测定3个反应器最后一格中厌氧污泥的比产甲烷速率,结果表明,ABR化粪池的厌氧污泥产甲烷的活性最好。此研究对传统化粪池的改造提出经济而行之有效办法,新型化粪池强化了化粪池出水的生化性和对污染物的去除,进而为化粪池的取舍和改造提供技术的参考依据。     

投加阳离子聚合物加速UASB反应器中颗粒污泥形成

运行2个UASB反应器,研究常温低浓度进水条件下,投加阳离子季胺盐絮凝剂对厌氧颗粒污泥形成的影响。一个反应器中投加阳离子季胺盐絮凝剂（称A反应器）,另一个反应器作为对照不投加絮凝剂（称B反应器）。经过196 d的运行,2个反应器中均形成了活性较高、沉降性能良好的颗粒污泥。A反应器中的污泥颗粒更多、粒径更大,粒径＞0.5 mm的污泥颗粒的百分比比B反应器的多16%～19.3%。研究结果表明,投加阳离子聚合物加速了颗粒污泥的形成,提高了颗粒污泥的产甲烷活性和沉降性能。     

糖蜜酒精废水厌氧可生化性实验研究

采用自制的球形反应器对糖蜜酒精废水进行厌氧可生化性研究.实验持续了40 d,CODcr从38 652 mg·L-1下降到6 094 mg·L-1,总去除率达84.23%.说明糖蜜酒精废水的厌氧可生化性较好;硫酸盐浓度由最初的3 860 mg·L-1下降到470 mg·L-1,去除率为87.82%.同时,有机污染物的去除高峰期比其硫酸盐延迟了2～4 d,说明可以通过控制运行反应条件和参数,对该废水采用两相厌氧处理工艺,在产酸相提前去除大部分的硫酸盐,减弱高浓度硫酸盐对厌氧反应的抑制作用.     

啤酒废水常温厌氧消化启动及运行实验

采用自行设计的复合式厌氧反应器在常温下对啤酒废水进行了厌氧发酵产沼气的实验研究,将进水COD控制在5 000 mg/L左右,采取逐步缩短HRT的方法来提高进水有机负荷,结果表明,启动运行41 d之后,产气量上升速度加快,反应器成功启动运行;在稳定运行过程中,随着负荷的升高,产气量呈阶梯式渐次上升,COD去除率保持在90%以上,出水pH值维持在7.0左右,TSS去除率达到60%以上,出水水质较好,说明该反应器具有较好的厌氧消化处理有机废水的能力。     

连续式两相厌氧消化的产气潜能

为了考察连续式两相厌氧消化过程及产酸相、产甲烷相最佳水力停留时间和产气潜能,并与序批式单相厌氧消化实验比较,采用生活垃圾、粪便、餐厨垃圾、污泥混合物料为消化原料,进行中温连续式两相厌氧消化和序批式单相厌氧消化实验。结果表明,单相厌氧消化产气潜能为242 m~3·t~(-1)TS,两相厌氧消化产气潜能达到380m~3·t~(-1)TS以上,提高了57.6%。两相厌氧消化最佳水力停留时间为14d,比单相厌氧消化的水力停留时间缩短了一半,并且连续式两相厌氧消化过程比单相厌氧消化具有更高的运行稳定性。     

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.