四川省毛河流域污染综合治理方案探讨

分析了四川省毛河流域各类污染源分布状况及水质现状,采用一维稳态单组分水质模型、多宾斯-坎普稳态模型,引入水文数据、水质监测数据、环境统计数据、社会统计公报数据,以Excel作为数据平台,对毛河水环境进行了动态模拟,反演出主要污染物降解系数。总结了毛河水环境目前存在的问题,并模拟计算了2种污染综合治理方案实施后对毛河水质的影响,确定了毛河流域水污染综合治理的重点以及制约因子。     

蚯蚓粪复配硼钼调理剂对土壤改良和茄子生长的影响作用

土壤质量决定着农产品的质量和农业生产的可持续发展,然而土壤退化成为农业生产的重要限制因素之一,施用土壤调理剂有利于减缓土壤退化的速度.该研究配制土壤调理剂,即蚯蚓粪?草菇渣?蛭石=6?3?1、钼酸钠50 g·kg?1、硼酸13.3 g·kg?1,并设5个不同的处理CK、QY-T1、QY-T2、QY-T3、QY-T4,研...     

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.     

Aflatoxin decomposition in various soils

Abstract

The persistence of aflatoxin in the soil environment could potentially result in a number of adverse environmental consequences. To determine the persistence of aflatoxin in soil, ¹⁴C‐labeled aflatoxin B₁, was added to silt loam, sandy loam, and silty clay loam soils and the subsequent release of ¹⁴CO₂ was determined. After 120 days of incubation, 8.1% of the original aflatoxin added to the silt loam soil was released as CO₂ ? Aflatoxin decomposition in the sandy loam soil proceeded more quickly than the other two soils for the first 20 days of incubation. After this time, the decomposition rate declined and by the end of the study, 4.9% of the aflatoxin was released as CO_2. Aflatoxin decomposition proceeded most slowly in the silty clay loam soil. Only 1.4% of aflatoxin added to the soil was released as CO₂ after 120 days incubation. To determine whether aflatoxin was bound to the silty clay loam soil, aflatoxin B₁ was added to this soil and incubated for 20 days. The soil was periodically extracted and the aflatoxin species present were determined using thin layer chromatographic (TLC) procedures. After one day of incubation, the degradation products, aflatoxins B₂ and G₂, were observed. It was also found that much of the aflatoxin extracted from the soil was not mobile with the TLC solvent system used. This indicated that a conjugate may have formed and thus may be responsible for the lack of aflatoxin decomposition.     

The effects of triclopyr on 2,4‐D mineralization in two soils

Abstract

The effects of the herbicide triclopyr (3,5,6‐trichloro‐2‐pyridinyloxyacetic acid) on the mineralization of 2,4‐D (2,4‐dichlorophenoyxacetic acid) in two soils which differed in their histories of prior exposure to the two herbicides were investigated. The relative effects of triclopyr on 2,4‐D mineralization and most probable numbers of 2,4‐D degraders were dependent upon the soil. Triclopyr was shown to increase 2,4‐D mineralization rates in a soil which had been exposed to both 2,4‐D and triclopyr, but decreased the mineralization rate of 2,4‐D and inhibited the increase of most probable numbers of 2,4‐D degraders in a soil that had not been directly exposed to either herbicide.     

石油工业废弃物处置及其生物治理趋势

鉴于我国石油工作者对石油工业废弃物的普遍关注，现在介绍生物治理的基本概念及ＳＰＥ石油工程师协会中有关含油污泥生物处置的途径及其突出优越性。生物液／固处理工艺（ＬＳＴ）是目前含油污泥处置现场最经济可行的处置方案。这种好氧的ＬＳＴ工艺过程，能够比较充分地代谢和降解石油污泥中的油和脂并大量除去多环芳烃类（ＰＡＨ）化合物及其它有机化合物，明显地降低了石油废弃物对人、畜的毒害程度。其工艺较简单，操作也简易，凡经此工艺处理后的废弃物不留残毒和后患，因此早已被世界上先进国家的炼油业视为处理含油污泥的有效选择了。石油工业废弃物的生物防治和生物降解工艺较大程度地领先于目前我国现场正在执行的各种处理含油废弃物的处理工艺。     

Fiscal incentives for Australian bushland

The clearing of over 80% of the native vegetation from Australian agricultural areas has contributed significantly to the degradation classification applied to more than half this land. Soil erosion, siltation, and salinity damage continue to increase yearly. This situation not only threatens the productivity of the farm sector but has contributed to the estimated loss of 78 species of native flora, endangerment of an additional 2206 species, and the loss of 20 species of Australia's marsupials.Private returns diverge from social returns because the action (or inaction) of farmers has an impact upon others, both now and in the future. There is justification, therefore, for the public sector to intervene on behalf of society in an attempt to influence private decision making for the social good. This article argues for increased incentives from the public sector in Australia to encourage the voluntary cooperation of farmers to improve the balance between development and conservation. In contrast to the essentially temporary nature of man-made measures such as flood-mitigating capital works, increasing the area set aside to native bushland offers scope for the permanent stewardship of the resource—land.     

高频超声波降解4-氯酚的反应机理及试验研究

探讨了高频超声波（1.7MHz)降解4-氯酚的反应过程和反应机理，研究了高频超声波降解4-氯酚的效果及4-氯酚的初始浓度，高级氧化方法（AOPs)等因素对降解效果的影响。试验结果表明，高频超声波降解4-氯酚为一级反应，超声波空化效应在降解过程中起主导作用。超声波与其他氧化方法联用可大大提高降解效率。具有良好的工业应用前景。     

Degradation of Monophenylheptamethylcyclotetrasiloxane and 2,6-cis-Diphenylhexamethylcycloterasiloxane in Londo Soil

The natural degradation of monophenylheptamethylcyclotetrasiloxane and 2,6-cis-diphenylhexamethylcyclotetrasiloxane in soil was evaluated under laboratory conditions. Both monophenyl and 2,6-cis underwent rapid degradation in dry soil generating the same products in varying proportions. During the first 24 hr, approximately 99% of the two materials underwent significant chemical transformations forming silanols of various structures, dimethyl cyclic siloxanes of the structure (Me₂SiO)x, and rearrangement products (geometrical isomers) of diphenylhexamethylcyclotetrasiloxane. Among the silanols, the following were identified as trimethylsilyl derivatives: HOSiMe₂OH, HOSiMePhOH, HOSiMe₂OSiMe₂OH, HOSiMePhOSiMe₂OH, HOSiMePhOSiMePhOH, HOSiMe₂OSiMe₂OSiMe₂OH, HOSiMePhOSiMe₂OSiMe₂OH, HOSiMe₂OSiMePhOSiMe₂OH, HOSiMePhSiMe₂OSiMePhOH, HOSiMePhOSiMePhOSiMe₂OH, HOSiMePhOSiMe₂OSiMe₂OSiMe₂OH, HOSiMe₂OSiMePhOSiMe₂OSiMe₂OH, HOSiMePhOSiMe₂OSiMePhOSiMe₂OH, HOSiMePhOSiMePhOSiMe₂OSiMe₂OH, HOSiMePhOSiMe₂OSiMe₂OSiMePhOH, HOSiMe₂OSiMePh-OSiMePhOSiMe₂OH. Derivatization was carried out using bis(trimethylsilyl)trifluoroacetamide. Gas chromatography-mass spectrometry and liquid chromatography-mass spectrometry (atmospheric pressure chemical ionization) analyses were used to derive structures. Structures were confirmed by gas chromatography-mass spectrometry comparisons of synthetic standards. Degradation was slower in wet soil. Nevertheless, in 14 days, the chemical transformation was essentially found to be complete as soil was allowed to dry. Detection of phenol as one of the degradation products revealed the occurrence of carbon–silicon bond cleavage promoted by soil.     

间接电化学降解亚甲基蓝废水的可行性研究

研究以ClO^-／Cl^-作媒介，间接电化学降解亚甲基蓝模拟废水的可行性。结果表明，亚甲基蓝的电化学降解与电极材料、电流密度以及添加剂种类等因素有关。以石墨为阳极，不锈钢为阴极，在无隔膜的烧杯中放置50ml浓度为1000mg/L的亚甲基蓝模拟废水，在室温25℃，pH6．0－8．0，槽电压10V，电流密度30．0mA/cm^2，Cl^-加入量2g/L的条件下，电解60min后，亚甲基蓝溶液的平均消色率达到98．0％，CODcr降解率为97．0％，BOD5降解率为99．0％；用浸涂过MnO2薄膜的石墨棒作阳极可显著加快其消解速率，而用浸涂过CeO2薄膜的石墨棒作阳极对其消解速率无明显的影响。并初步讨论了其降解机理。