用铁泥制备高效无机絮凝剂聚硅酸铁及其絮凝性能研究

研究了以铁泥、硅酸钠为原料,制备高效絮凝剂聚硅酸铁(PSF)的方法,确定了合理的生产工艺和操作条件.并对絮凝剂PSF处理工业废水的絮凝性能进行了研究,探讨了PSF处理工业废水的反应机理.结果表明,PSF具有良好的絮凝性能,是一种比聚合硫酸铁(PFS)性能更优良的絮凝剂.     

天然高分子改性阳离子絮凝剂的合成及对工业废水的处理

以天然高分子F691粉为原料，合成了一种阳离子絮凝剂FIQ－C，考察了各种因素对合成的影响，并研究了它对工业废水的处理效果。研究结果表明，在最佳合成条件，FIQ－C具有良好的絮凝性能。FIQ－C与PAC复制便利地，对工业废水处理效果最好，废水处理后可达标排放。     

微生物絮凝反应动态模拟水质模型

探讨了以硫酸盐还原菌为生物絮凝剂处理工业废水的效果，并进行了动态中试研究，以寻求应用于工程实际的技术参数。系统分析了影响处理效果的主要因素，得出了最佳工艺条件，并进一步尝试将絮凝理论，生化理论与水力学动态平衡理论结合起来，推出多因子相关的絮凝反应动态模拟水质模型，为该技术应用于工程自动控制提供一定的理论依据。     

利用啤酒废水所产微生物絮凝剂处理靛蓝印染废水的研究

以啤酒废水为培养基，利用其中的碳源和能源，对复合菌群进行发酵培养，制得微生物絮凝剂。将此絮凝剂处理靛蓝印染废水．系统研究了pH、微生物絮凝剂用量和助凝剂（1?Cl2溶液）用量对处理效果的影响，得出了微生物絮凝剂去除CODCr和脱色的最佳工艺条件，并对该絮凝剂的絮凝机理进行了初步探讨。     

壳聚糖复合絮凝剂处理造纸废水的实验研究

研究并考察了壳聚糖复合絮凝剂对造纸污水中COD和SS的絮凝效果，结果表明，当复合絮凝剂的配方和处理条件为：聚合硫酸铁（PFS）60 mg/L聚丙烯酰胺（PAM）2 mg/L壳聚糖（CTS）0.4 mg/L，pH为7.5时，其絮凝效果最佳，此时它对水中COD与SS的去除率分别达到57.4%和97.6%, 与传统絮凝剂PAC/PAM相比，COD与SS的去除率分别提高了10.1%和5.2%，药剂成本下降了21.1%，具有明显的经济效益与环境效益。     

羧甲基壳聚糖的制备及絮凝性能探讨

制备了具有水溶性、无毒羧甲基壳聚糖（以下简称NOCC），将其作为絮凝剂与聚丙烯酰胺（PAM）一道处理生活污水，通过测定其沉降时间，沉降絮体高度，沉降速度，沉降后溶液透光率等参数，表征了其絮凝能力，提出了普遍认为聚丙烯酰胺处理一般污水具有良好絮凝能力的不同看法，为壳聚糖的开发利用做了有益的探索。     

青霉菌HHE-P7利用酱油废水产生微生物絮凝剂的研究

研究了微生物絮凝剂产生菌HHE-P7在酱油废水中产生微生物絮凝剂的絮凝特性。实验表明，酱油废水由于碳源丰富，是一种良好的培养基。HHE-P7菌最佳培养条件为：COD20000mg／L，K2HP041．0g／L，培养3d。最佳絮凝条件为在1L高岭土水中投加10～15mL微生物絮凝剂（MBF7），pH调至9，则絮凝率为90％以上；微生物絮凝荆在水系中主要起吸附架桥的作用。     

聚硅酸锌铝的制备及其性能研究

以硅酸钠、硫酸锌、硫酸铝为原料，通过共聚法制备了无机高分子絮凝剂聚硅酸锌铝（PSZAS），研究了Na₂SiO₃的摩尔浓度、活化时间、Al/Si、Zn/Si 配比及絮凝剂的投加量对絮凝效果的影响，用X-射线衍射（XRD）和电子扫描电镜（SEM）对该絮凝剂的结构及形貌进行了表征。结果表明：当硅酸钠的浓度为0.4 mol/L，硅酸活化时间为2 h，Si∶Al∶Zn=1∶1∶1.5，絮凝剂投加量为20 mL/L废水时，絮凝剂的电中和能力和吸附架桥能力最强，絮凝剂对含H-酸染料模拟废水的絮凝效果最好。     

采用泥回流处理彩色显像管含氟废水

本文通过中和、混凝沉降法除氟过程，研究了彩色显像管工业废水除氟的适宜工艺条件，现场试验表明：应用泥回流处理技术，采用高效絮凝剂处理含氟废水，排放废水氟含量可稳定在4-6mg/L之间，低于排放标准（10mg/L），同时废水处理的成本大大降低。     

壳聚糖衍生物-镁盐复配去除中性兰模拟废水色度的研究

研究了有机高分子絮凝剂NCTS-M对中性兰染料的絮凝性能。通过测量絮体的Zeta电位以及对絮体进行彩色电视显微扫描初步探讨了该絮凝过程的絮凝机理。结果表明，当投加量为30 mg/L，pH=6时，絮凝效果最明显，脱色率可达93.1%。其絮凝机理主要是压缩双电层以及高分子吸附架桥作用，以压缩双电层为基础。絮凝剂中镁离子在中性条件下对絮凝过程也起到了较强的助凝作用。     

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.     

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.