抚仙湖北岸入湖径流中总氮变化趋势分析

抚仙湖现有污染主要来自北岸。通过抚仙湖3条入湖河流中总氮负荷量进行调查，对抚仙湖入湖河流中总氮负荷量进行了分析评价，结果表明：3条入湖河流总氮为劣V类水质，是影响抚仙湖水质的主要因素。为湖泊总量控制与治理提供科学依据。     

再生铅冶炼对土壤环境影响及其评价和环境管理

再生铅冶炼是对废弃物的循环利用,防治铅污染的重要手段,但冶炼中处置不当,会引起土壤污染,再生铅冶炼对土壤环境的影响,首先进行环境影响识别,并根据冶炼中铅的排放强度和铅的生物地球化学循环规律来阐明其排放特点和进入土壤的途径,通过再生铅冶炼项目环境影响评价的实例,探讨了土壤环境质量的现状分析、评价和预测等研究方法,并提出严格执行环境影响评价制度和“三同时”制度,强化建设项目本身的环境管理和完善土壤环境质量标准等土壤环境管理措施。     

黄土高原地区水资源合理利用

黄土高原地区自然资源丰富，但生态环境脆弱。区内既有巨大的开发任务，又有严重的环境整治问题，它们都需要大量的供水。该区地处干旱半干旱地区，水资源较贫乏，供需矛盾尖锐。针对地区水资源特征及需水特点，本文提出了水资源开发利用以节水与开发结合，开发利用与保护并重的措施，确保水资源能得到永续利用。     

环境生物技术

环境生物技术作为一门新兴边缘学科在解决环境污染问题上具有很大的潜力。主要介绍了环境生物技术在各方面的研究应用进展 ,并指出环境生物技术的发展趋势和应用前景     

Assessment of global industrial-age anthropogenic arsenic contamination

Arsenic, a carcinogenic trace element, threatens not only the health of millions of humans and other living organisms, but also global sustainability. We present here, for the first time, the global industrial-age cumulative anthropogenic arsenic production and its potential accumulation and risks in the environment. In 2000, the world cumulative industrial-age anthropogenic arsenic production was 4.53 million tonnes. The world-wide coal and petroleum industries accounted for 46% of global annual gross arsenic production, and their overall contribution to industrial-age gross arsenic production was 27% in 2000. Global industrial-age anthropogenic As sources (as As cumulative production) follow the order: As mining production >As generated from coal >As generated from petroleum. The potential industrial-age anthropogenic arsenic input in world arable surface in 2000 was 2.18 mg arsenic kg^–1, which is 1.2 times that in the lithosphere. The development of substitute materials for arsenic applications in the agricultural and forestry industries and controls of arsenic emissions from the coal industry may be possible strategies to significantly decrease arsenic pollution sources and dissipation rates into the environment.     

渤海海域船舶防污设备铅封的可行性

从船舶排污口确认、船舶防污设备铅封要求和方法等方面，介绍说明渤海海域船舶防污设备铅封的可行性。     

Comparison of Black Carbon,Total Organic Carbon,and PAH Concentrations in Surface Sediments from Two Main Rivers in Henan Province,China

Black carbon (BC) in surface sediments from Henan section of Yellow River and Huaihe River, China, was determined. Average content of BC in Huaihe River was 0.33%, higher than that in Yellow River (n?=?23) with mean value of 0.15%. Distribution patterns of BC in Yellow River and Huaihe River were similar, namely that tributaries had higher BC content than main stream. In addition, BC content in the mainstream of Yellow River and Huaihe River decreased with altitude. The BC content presented a significant positive correlation with clay (r?=?0.672; p?<?0.01) content in Yellow River, while neither did in Huaihe River. The ratio of BC/TOC ranged from 1.8–57.4% (median 29.6%), evidencing pyrogenic fossil fuel source of BC in Yellow River. Relatively low values of BC/TOC in Huaihe River (5.3%–28.8%, median 7.5%,) reflected that the origin of BC is from burning of biomass. In addition, Pearson rank correlation analysis showed that BC was in strong correlation with lighter PAH in Yellow River, while BC was in significant correlation with heavier PAH in Huaihe River. The ratio of BC/TOC indicated that BC in Yellow River mainly came from fossil fuel combustion, while BC in Huaihe River was primarily from biomass burning.     

Selective extraction of trace mercury and cadmium from drinking water sources.

In this paper, a new alternative method, i.e., selective extraction by weakly basic anion exchange resin, has been developed for the removal of trace cadmium and mercury ions from drinking water sources. The mechanism of heavy metal removal is based on selective extraction as the results of LEWIS-base-acid interactions. Transfer of trace mercury species from liquid to resin phase coincides well with the performance of film diffusion. The results demonstrated that the presence of chlorine has a negligible influence on the removal of mercury. However, humic acids can strongly bind mercury by the formation of complex compounds and therefore become the obstacle in the diffusion progress. At neutral or base pH, the resin material exhibits the favorable uptake of heavy metals. In filter experiments, the studied resin material offers favorable properties in the selective extraction of trace mercury and cadmium.     

The photocatalytic disinfection of urban waste waters

In this paper we present the results of the photocatalytic disinfection of urban waste water. Two microbial groups, total coliforms and Streptococcus faecalis, have been used as indexes to test disinfection efficiencies. Different experimental parameters have been checked, such as the effect of TiO2, solar or UV-lamp light and pH. Disinfection of water samples has been achieved employing both UV-lamp and solar light in agreement with data shown by other authors. The higher disinfection rates obtained employing an UV-lamp may be explained by the stronger incident light intensity. Nevertheless no consistent differences have been found between TiO2-photocatalysis and direct solar or UV-lamp light irradiation at natural sample pH (7.8). At pH 5 the presence of TiO2 increases the relative inactivation rate compared with the absence of the catalyst. After the photocatalytic bacterial inactivation, the later bacterial reappearance was checked for total coliforms at natural pH and pH 5, with and without TiO2. Two h after the photocatalytic treatment, CFU increment was almost nill. But 24 and 48 h later an important bacterial CFU increment was observed. This CFU increment is slower after irradiation with TiO2 at pH 5 in non-air-purged samples.     

Photochemical reduction of hexavalent chromium in glycerol-containing solutions

Hexavalent chromium [Cr(VI)] in the form of potassium dichromate was photochemically reduced to trivalent chromium [Cr(III)] in aqueous solutions containing glycerol. This reaction occurred rapidly during irradiation with either unfiltered sunlight or a UVA-emitting light source. Photochemical reduction of Cr(VI) was pH-dependent and did not occur in dilute solutions of sodium hydroxide. In acidified solutions, the reduction occurred at elevated rates and at lower concentrations of glycerol. This reaction was found to be dependent on the unsubstituted alcohol groups of glycerol since alpha-phosphoglycerol and beta-phosphoglycerol did not support the photochemical reduction of Cr(VI). These findings suggest that glycerol or related polyols can be used for the remediation of hexavalent (toxic) chromium at contaminated environmental sites.