进口废塑料环境保护管理研究

随着塑料资源的大量消耗,废塑料的利用引起了社会的高度重视。工艺简单,投入成本少,入行门槛低导致部分废塑料加工利用企业技术水平低、管理模式差、环境污染重。为规范进口废塑料行业,通过调研统计、实验分析、咨询论证和研究了进口废塑料环境保护管理规定,对进口废塑料企业的规模、设备、人员和管理等方面提出了要求,为进一步规范提升进口废塑料行业提供技术支撑。     

宁波南沙港网箱养殖水域营养状况评价及生物修复策略

根据2007年1月-2007年11月4个航次对宁波南沙港网箱养殖水域水体营养盐（NO2--N、NO3--N、NH 4＋-N和PO34--P）含量的监测结果,利用营养指数E法对水体的富营养化状态进行了评价。根据网箱养殖系统物质平衡方程和现场调查实验数据,估算了南沙港网箱养殖水域的氮磷污染负荷,以溶解态氮作为平衡指标,估算了鱼藻类合理的配比模式。结果表明,南沙港水体中NO2--N、NO3--N、NH4＋-N、PO4-P含量年变化范围分别为0.26μmol/L～4.86μmol/L,33.93μmol/L～82.86μmol/L,0.59μmol/L～7.86μmol/L,1.47μmol/L～2.97μmol/L,不同养殖区之间营养盐含量差异不显著（p〈0.05）;营养指数E值年变化范围介于2.41～15.99之间,表明该港水体处于重度富营养化状态;养殖区N/P值的年平均值为32.95,表明南沙港海区是一个氮过剩的养殖系统。南沙港网箱养殖水域氮、磷的负荷量分别为70.43 t/a和5.96 t/a,其中溶解态氮、磷负荷量分别为49.3 t/a和2.38 t/a;南沙港的藻类养殖面积需要在现有基础上再扩大0.44倍,达到107.52 ha,才可以与网箱养殖系统的氮磷污染负荷构成平衡;网箱养殖个数与藻类养殖面积（ha）的合理配比约为1∶0.027。     

混合菌利用制酒废水产生的微生物絮凝剂的成分及理化特性研究

对蜡状芽孢杆菌(Bacillus cereus)和膜璞毕赤酵母菌(Pichia membranifaciens)混合后利用制酒废水作为替代培养基产生的复合型微生物絮凝剂XJBF-1进行了成分及理化特性研究。结果表明,XJBF-1的主要成分是多糖(质量分数为63.40%),总蛋白质质量分数仅为0.87%;XJBF-1为线型结构,分子量仅为50 798u,低于一般的微生物絮凝剂;XJBF-1具有较好的热稳定性,这一特性有利于絮凝活性物质的提取和纯化;XJBF-1对糖化酶作用敏感,而对蛋白酶作用不敏感;XJBF-1对鱼苗基本没有急性毒性,可以作为无毒水处理剂使用。     

Exploring the relationship between vegetation spectra and eco-geo-environmental conditions in karst region, Southwest China

Remote sensing of local environmental conditions is not accessible if substrates are covered with vegetation. This study explored the relationship between vegetation spectra and karst eco-geo-environmental conditions. Hyperspectral remote sensing techniques showed that there were significant differences between spectral features of vegetation mainly distributed in karst and non-karst regions, and combination of 1,300- to 2,500-nm reflectance and 400- to 680-nm first-derivative spectra could delineate karst and non-karst vegetation groups. Canonical correspondence analysis (CCA) successfully assessed to what extent the variation of vegetation spectral features can be explained by associated eco-geo-environmental variables, and it was found that soil moisture and calcium carbonate contents had the most significant effects on vegetation spectral features in karst region. Our study indicates that vegetation spectra is tightly linked to eco-geo-environmental conditions and CCA is an effective means of studying the relationship between vegetation spectral features and eco-geo-environmental variables. Employing a combination of spectral and spatial analysis, it is anticipated that hyperspectral imagery can be used in interpreting or mapping eco-geo-environmental conditions covered with vegetation in karst region.     

浅谈测井事故的认识与处理

在测井过程中,由于各种不可预见的复杂原因,测井事故不可避免。文章分析了形成测井事故的影响因素,如井径、钻井液性能、全角变化率、操作过程、套管鞋等。一旦测井事故发生,根据卡电缆、卡仪器、断电缆的事故特点来判断事故类型,再根据各种处理方法的优缺点来处理事故;提出一些注意事项,使测井事故防患于未然。     

Removal of polycyclic aromatic hydrocarbons from aqueous solution on soybean stalk-based carbon

Soybean [ (L.) Merr.] stalk-based carbons were prepared by phosphoric acid activation at different carbonization temperatures. Characteristics of the prepared carbon, including specific surface area, iodine number, and amount of methylene blue sorption, were determined. Experiments on phenanthrene, naphthalene, and acenaphthene, as representatives of polycyclic aromatic hydrocarbons (PAHs), removal from aqueous solution by the prepared carbon were conducted at different levels of carbon addition. The results indicated that the specific surface area, iodine number, and amount of methylene blue sorption increased with an increase of carbonization temperature. The maximum values were observed at 700°C and were 287.63 m g, 508.99 mg g, and 90.14 mg g, respectively. The removal efficiencies of phenanthrene, naphthalene, and acenaphthene tended to increase with increasing carbon amounts and carbonization temperature. The optimal removal performance was obtained under the experimental conditions of carbon concentrations of 0.04 g 32 mL and carbonization temperature of 700°C, and the removal efficiencies of phenanthrene, naphthalene, and acenaphthene were 99.89, 100, and 95.64%, respectively. The performance of the prepared carbon was superior to that of commercial activated carbon. Additionally, for the same carbon concentrations, the removal efficiency of PAHs on prepared carbons followed the order: phenanthrene > naphthalene > acenaphthene. Results obtained from this work provide some insight into the reuse of an agricultural residue, and also provide a new application for the treatment of PAHs in contaminated water utilizing activated carbon prepared from agricultural residues.     

Distribution, sources, and potential risk of polycyclic aromatic hydrocarbons (PAHs) in drinking water resources from Henan Province in middle of China

Distribution and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in drinking water resources have been carried out for the first time in Henan Province, China. Water samples collected from four river systems and their tributaries, as well as groundwater resources, were analyzed according to EPA method 525.2. Total of 68 water samples were collected in 18 cities in Henan province in May, August and November, 2001. Concentrations of sum of 16 priority PAHs in water samples ranged from 15 to 844 ng/L with a mean value of 178 +/- 210 ng/L (n = 68). The spatial and temporal distribution of PAHs showed that the Huanghe and the Huaihe river systems had relatively higher concentrations of total PAHs. Higher concentrations of total PAHs were observed in August and November than in May, with respective mean values of 262, 232 and 33.6 ng/L. Ratios of Ant/(Ant + Phe) and Flur/(Flur + Pyr) were calculated to evaluate the possible sources of PAH contamination, which indicated that the coal combustion sources were the main contributors to PAHs in most drinking water resources. Some petrogenic (or pyrolytic) sources of PAHs were also found. The toxic equivalency factors (TEFs) were used to calculate benzo[a]pyrene equivalents (BaPE) for water samples. The average value of BaPE was 0.6 ng/L. The values in most stations were much lower than the guideline values in drinking water of Chinese Environmental Protection Agency (CEPA, 2.8 ng/L) and the US Environmental Protection Agency (US EPA, 200 ng/L). Overall, the drinking water resources in Henan province showed some carcinogenic potential.     

CS2在TiO2表面的多相光化学反应研究

本文运用原位漫反射红外光谱(DRIFTS)、GC、XPS等手段研究了CS2在大气半导体颗粒TiO2表面的多相光化学反应.结果表明在模拟太阳光照射下,低浓度的CS2(8.1 mg·m(-3))在TiO2:表面发生多相光化学反应,生成气态产物cos、H2S、SO2,进而在颗粒物表面生成硫酸盐.在氧气体积浓度为21%,氙灯照...     

Optimization of bio-drying of kitchen waste: inoculation,initial moisture content and bulking agents

Journal of Material Cycles and Waste Management - Bio-drying has been proved to be a promising method for treatment of MSW (municipal solid waste) and sewage sludge due to its high energy...     

Identification of sources of elevated concentrations of polycyclic aromatic hydrocarbons in an industrial area in Tianjin, China

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) were determined by gas chromatography equipped with a mass spectrometry detector in 105 topsoil samples from an industrial area around Bohai Bay, Tianjin in the North of China. Results demonstrated that concentrations of PAHs in 104 soil samples from this area ranged from 68.7 to 5,590 ng g^???1 dry weight with a mean of ∑16PAHs 814 ± 813 ng g^???1, which suggests that there exists mid to high levels of PAH contamination. The concentration of ∑16PAHs in one soil sample from Tianjin Port was exceptionally high (48,700 ng g^???1). Ninety-three of the 105 soil samples were considered to be contaminated with PAHs (>200 ng g^???1), and 25 were heavily polluted (>1,000 ng g^???1). The sites with high PAHs concentration are mainly distributed around chemical industry parks and near highways. Two low molecular weight PAHs, naphthalene and phenanthrene, were the dominant components in the soil samples, which accounted for 22.1% and 10.7% of the ∑16PAHs concentration, respectively. According to the observed molecular indices, house heating in winter, straw stalk combustion in open areas after harvest, and petroleum input were common sources of PAHs in this area, while factory discharge and vehicle exhaust were the major sources around chemical industrial parks and near highways. Biological processes were probably another main source of low molecular weight PAHs.