氧化镁烟气脱硫反应特性研究

利用实验室规模的鼓泡式反应装置,对比了碳酸钙、氧化镁和氧化镁/硫酸镁脱硫剂的反应活性,证实脱硫液中高浓度硫酸镁的存在是保证镁法脱硫效率高于钙法的重要因素,并考察了硫酸镁浓度、脱硫剂(氧化镁)浓度、烟气量、SO2浓度和吸收液温度等因素对脱硫效率的影响。结果表明,脱硫反应可以根据pH分为2个不同阶段;反应过程中脱硫效率随着硫酸镁浓度的增加而显著升高;烟气量增加将会导致脱硫效率有所下降;入口SO2浓度升高,脱硫效率下降;氧化镁浓度、温度对脱硫效率影响不显著。结合实验现象进行推断,氧化镁脱硫的反应过程受SO2在气液两相界面的传质扩散和其水解产物在液相的扩散控制。     

氧化镁强化浓海水吸收低浓度二氧化硫的实验研究

研究了添加氧化镁强化后浓海水对低浓度二氧化硫的吸收效果。利用鼓泡吸收装置考察了不同氧化镁投加量、气体流速和吸收液温度对二氧化硫吸收效果的影响。结果表明,氧化镁可以极大地提高吸收液的脱硫效率。在室温,氧化镁投加量为0.5 g/L时,吸收体系对二氧化硫的吸收效果最好,吸收容量达到1 901.38 mg/L,是普通海水脱硫和未加添加剂的3～6倍。     

软锰矿催化氧化脱除烟气中的SO2

对软锰矿催化氧化法去除烟气中SO2的方法进行了探索，研究了各工艺参数对烟气中SO2去除率的影响。结果表明：MnO2与Mn^2 的催化效果较好，传质过程对脱硫过程的影响较大，软锰矿浆在合适条件下能有效吸收低浓度的SO2。     

柠檬酸强化钢渣湿法烧结烟气脱硫及机理

在鼓泡反应器中考察了添加柠檬酸强化钢渣湿法烧结烟气脱硫的影响因素,包括钢渣粒度,吸收浆液浓度、进口二氧化硫浓度、停留时间,p H值,柠檬酸与钢渣的浸泡时间等,结果表明,柠檬酸浓度为2.0 mmol/L、钢渣浓度为4%、二氧化硫进口浓度为1 500 mg/m3、烟气停留时间为7 s、钢渣强化时间为2 h、钢渣粒度200目,脱硫率达到90%以上。经4 mmol/L的柠檬酸强化后的钢渣浆液脱硫率比单纯钢渣浆液提高18.41%,达到90.99%的脱硫率,且有效反应时间延长50%,达到60 min以上。柠檬酸的加入,一方面促进了钢渣碱性组分溶解,另一方面在吸收液中形成柠檬酸和柠檬酸盐缓冲体系,增加了气液界面SO2浓度,提高了SO2的气液传质速率。     

低温结晶净化柠檬酸盐解吸贫液中硫酸根

在柠檬酸盐吸收—解吸脱硫技术中,完成循环吸收过程的吸收液由于烟气杂质催化和高温解吸变成了含低二氧化硫浓度、中高硫酸根浓度、多种有机酸共存的柠檬酸盐解吸贫液,造成吸收效率下降、SO2平衡容量严重降低,必须进行溶液净化,特别是净化硫酸根。针对这一问题,实验室采用低温结晶法净化柠檬酸盐脱硫解吸贫液模拟液,通过对溶液中硫酸根浓度分析,研究了不同反应时间、温度、初始硫酸根浓度、柠檬酸根总浓度和溶液p H对硫酸根去除效率的影响。结果表明,硫酸根去除率与冷冻温度和溶液p H有关。在柠檬酸根总浓度1.5 mol/L,初始硫酸根浓度40 g/L,冷冻温度3℃,p H 4.5的条件下,可将硫酸根净化至16.9 g/L。     

超重力旋转填料床在燃煤尾气处理上的应用进展

本文指出了我国燃煤尾气脱硫进展缓慢的原因 ,介绍了一种新型的燃煤尾气脱硫设备———超重力旋转脱硫床的工作原理、传质特性及在低浓度的废气处理上的广阔应用前景     

电化学法脱除烟气二氧化硫制取硫酸-Br-/Br2电解体系

本文研究了Br-/Br2体系的电化学方法脱除烟道气中二氧化硫的各个影响因素:温度对电解体系的性能影响;温度、酸度以及吸收方式对脱硫效率的影响.     

电化学法脱除烟气二氧化硫制取硫酸-Br-/Br2电解体系

本文研究了Br-/Br2体系的电化学方法脱除烟道气中二氧化硫的各个影响因素:温度对电解体系的性能影响;温度、酸度以及吸收方式对脱硫效率的影响.     

脱硫灰中杂质对石灰石脱硫活性的影响

研究脱硫灰中杂质对石灰石脱硫活性的影响具有重要意义,采用烟气湿法脱硫用石灰石粉反应速率的测定方法,使用瑞士万通902智能电位滴定仪,分析了SiO2、Al2O3、Fe2O3、CaSO3与MgO等脱硫灰中5种杂质对石灰石脱硫活性的影响。结果表明,在实验浓度范围内,SiO2、Al2O3、CaSO3的加入在一定程度上促进了石灰石的溶解,而MgO、Fe2O3的加入在一定程度上抑制了石灰石的溶解。将脱硫灰与石灰石掺合作脱硫剂时,要综合考虑这5种杂质对石灰石溶出的影响,选择适宜的脱硫灰和石灰石掺合比。     

电化学法脱除烟气二氧化硫制取硫酸—Br^—／Br2电解体系

本文研究了Ｂｒ＾－／Ｂｒ２体系的电化学方法脱除烟道气中二氧化硫的各个影响因素：温度对电解体系的性能影响;温度、酸度以及吸收方式对脱硫效率的影响。     

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.