应用复合碱式氯化铝对垃圾渗沥液进行预处理的研究

采用生物法处理垃圾渗沥液,其出水CODCr、色度和含盐量等指标往往大于排放标准。应用亚滤技术作深度处理,可有效地去除剩余的污染物质,使出水达标。但由于渗沥液中存在大量的胶体微粒,对亚滤管产生阻垢作用,从而堵塞住住亚滤管微也,增加动力消耗,影响处理效果。故采用一种新型高效的复合型无机高分子混凝剂－－聚硫氯化铁铝（PAFCS）用于亚滤装置的预处理。通过与碱式氯化铝（PAC）混凝剂的对比研究表明,PAFCS表现出比PAC更好的除浊、脱色能力,可有效地去除掉垃圾渗沥液中的浊度、胶粒和部分CODCr,从而使亚滤装置发挥最大效能。结果表明,PAFCS的投加量在150－200mg/L左右,pH值在5左右,沉降时间为40－50min的条件下,混凝效果最佳,浊度去除率可达到90％,CODCr去除率可达40％左右。     

用聚硅酸铁铝对垃圾渗沥液进行预处理的研究

采用一种新型高效的无机高分子混凝剂——聚硅酸铁铝(PSAF)用于垃圾渗沥液亚滤装置的预处理。结果表明，在PSAF的投加量为150mg/L，pH为5．0和沉降时间为60min的条件下，混凝效果最佳，浊度去除率可达92％左右，色废去除率可达91％左右，CODcr去除率可达70％左右。同时探讨了该混凝剂处理垃圾渗沥液的反应机理。     

陶瓷印花废水处理的混凝剂及工艺条件

采用混凝剂聚合氯化铝（PAC）、聚丙烯酰胺（PAM）、聚合硫酸铁（PFS）对陶瓷印花废水进行混凝沉降处理，监测水样的吸光度、浊度、悬浮物，以脱色率、浊度去除率、悬浮物去除率评价混凝处理的效果。结果表明：PAC是陶瓷印花废水沉降处理的理想混凝剂；水样的吸光度、浊度、悬浮物随混凝剂用量增大和沉降时间延长而呈降低趋势，而脱色率、浊度去除率、悬浮物去除率随混凝剂和沉降时间的增大呈增大的趋势；PAC投加量为20mg／L，沉降时间约为24h，水样脱色率达到90．0％，而当PAC投加量达到100mg／L，沉降时间约为4h，陶瓷印花水的脱色率可达到96．0％。证明了药剂用量的增加与沉降时间的延长对混凝过程具有增效作用。     

FIBAX纤维滤料在再生水工艺中的应用研究

针对某化工厂甲醇冷凝液再生处理工艺中生化出水浊度较高,对后续离子交换树脂产生不利影响等问题,考察了新型FIBAX纤维过滤对浊度的去除情况.当采用微絮凝后FIBAX过滤(滤速50 m/h)时,混凝剂PAC最佳投加量2 mg/L(以Al2O3计),其对浊度的去除率为99.9%,出水浊度达到小于0.50 NTU的目标要求,此时其过滤周期36 h,并且其投资和运行费用均较低.上述结果表明,FIBAX纤维滤料能有效去除来水中的细少悬浮物,满足后续工艺要求,是一种新型的固液分离材料.     

不同混凝剂处理松花江低温水

东北松花江地区冬季有将近6个月的冰封期,低温季节水源水处理难度大。为了保证东北地区冬季饮用水供应,研究几种混凝剂在处理冬季松花江低温水时的混凝效果。实验结果表明,NPAC1和NPAC2水解产物中具有较高的Alb和Alc成分,拥有较高的电中和、吸附和网捕卷扫性能,高效聚铝铁(PAF)水解产物Fe(OH)3具有比表面积大、吸附架桥作用较强的优点。这3种混凝剂无论是在控制出水浊度还是在对水体有机物去除能力方面均优于目前水厂所使用的PAC和聚合氯化铝铁(水厂PAF);NPAC2的投加量达到50 mg/L时,出水浊度达到最优;当混凝剂投加量达到50 mg/L时,NPAC1的浊度去除率逐渐超过NPAC2,剩余浊度低于3.0 NTU;NPAC1、NPAC2和PAF 3种混凝剂对有机物的去除能力大致相当,当混凝剂投加量为50 mg/L时,这3种混凝剂处理后的水的UV254的值均低于0.06,而水厂使用的2种混凝剂处理后的水的UV254仍高于0.1;结合其对浊度去除的情况,可以判断55 mg/L的投药量为NPAC1的最优投药点,PAF的最佳投药量为65 mg/L;投加适量的粉末活性碳可以有效地提高氨氮的去除率,当粉末活性炭的投加量为30 mg/L时,氨氮的去除率基本达到最大(51.27%)。表面负荷对混凝效果具有重要的影响,合理降低沉淀池的表面负荷对于提高出水水质具有重要作用。     

网络版论文摘要

垃圾填埋场渗滤液后处理的研究柴晓利　赵由才(同济大学污染控制与资源化研究国家重点实验室 ,上海 2 0 0 0 92 )采用混凝絮凝法对经生化处理后的垃圾渗滤液进行后处理。结果表明 ,混凝絮凝法对难降解有机质的去除十分有效 ,CODCr去除率可达 6 0 %以上。特别是微生物絮凝剂由于用量少 ,不产生二次污染 ,可应用于垃圾渗滤液特别是给水难降解有机质的去除工艺中。关键词 :絮凝剂 ,垃圾渗滤液 ,混凝絮凝法。粉煤灰混凝剂的制备和预处理印染废水的试验研究李　磊　赵玉明(南京大学环境学院污染控制与资源化研究国家重点实验室 ,南京 2 10 0 93…     

铁铝复配混凝剂处理低温低浊水

针对北京某水库水在冬季呈现低温低浊特性,以此为原水的某水厂在该期间常会出现出水余铝超标现象的问题,通过烧杯实验研究不同投药量下聚合氯化铝(PAC)以及它与三氯化铁(FeCl3)不同复配比形成混凝剂对冬季北京某水库水的处理效果。结果表明,复配药剂存在最佳的Fe/Al摩尔复配比为1/5,此时余铝、有机物去除效果较其他配比混凝剂高。在此配比下,当PAC投药量为0.03 mmol/L时,水中残余铝量取得最低值0.0063 mg/L。相同投药量复配药剂的浊度去除效果比单独使用PAC的浊度去除效果略弱。当投药量为0.06 mmol/L时,Fe/Al摩尔比为1/5的复配混凝剂,能使浊度降至0.4 NTU左右。此外,复配药剂的投药量小,投药范围更宽,易于实际投药操作;同时复配药剂还适于常温及偏中性水源水的处理。规模为5 m3/h中试实验也证明,采用铁铝复配混凝剂连续运行,可获得良好的浊度、余铝去除效果。     

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。     

新型聚合铝硅混凝剂处理洗浴废水的试验研究

针对常规铝盐、铁盐去除洗浴废水中阴离子洗涤剂 (LAS)效果不理想的状况 ,采用高碱化度钙型聚合铝硅混凝剂 (CPASC)进行了试验研究 ,同时与聚合氯化铝 (PAC)作了比较。结果表明 ,该混凝剂对洗浴废水中COD、LAS、SS及浊度都有较高的去除率 ,特别对LAS、COD的去除率分别比PAC高 10 %和 8%以上。当投加量为 6 0mg/L时 ,出水各项指标均达到生活杂用水水质标准 (GJ2 5 .1 89)。     

地表水中隐孢子虫和贾第鞭毛虫微球的混凝去除

以向地表水中投加的隐孢子虫微球和贾第鞭毛虫微球为对象,研究通过对给水混凝工艺对其的去除效果进行比较,着重考察了不同混凝剂种类、投加量及水样pH值对去除效果的影响.结果表明,混凝工艺可较为有效地去除地表水中的两虫微球,去除率最高可达4 lg.相比常规的金属盐类混凝剂,高分子的PAC、PAFC混凝剂对两虫微球的混凝去除率更...     

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.     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

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.     

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.     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

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.