秸秆焚烧对玉溪市大气PM10的影响解析研究

以水溶性钾为示踪元素,解析秋收季节秸秆焚烧对玉溪市大气PM10的贡献.结果表明,2001年秋收季节(10月)水溶性钾浓度(7.68μg/m3)比夏季水溶性钾浓度(2.38μg/m3)高3.2倍,与7月至12月份PM10浓度变化呈显著相关,相关系数为0.810.很显然,秋收季节秸秆焚烧对玉溪市大气PM10有负面影响.     

GPS/GSM/GIS海上溢油跟踪监测系统的研究

在车载GPS监控系统的基础E研究开发了一种漂浮移动性能与溢油相似的、并具有GPS接收和发送功能的GPS浮标。在溢油事故发生后立即将其投放存厚油膜层中随油膜一起漂移。监测中心通过GSM移动通信网实时接收GPS浮标发出的定位信息，并应用地理信息系统技术实现对溢油位置、漂移速度、轨迹、方向的实时跟踪和信息显示．从而为溢油应急指挥提供一种准确实时、成本低廉、全天候的溢油全程监测手段。     

高浓度苯酚在石墨电极上电解特性的研究

研制了数据在线采集记录系统对高浓度苯酚在石墨电极上电解过程的循环伏安行为进行了研究。采用连续循环伏安法考察了体系电解的特点,并考察了支持电解质、扫描速率、苯酚的浓度对反应体系的影响。结果表明:峰电流密度与扫描速率的平方根及苯酚浓度呈线性递增关系,支持电解质的添加量在苯酚电解过程存在最佳值,多次扫描过程中峰电流密度有下降趋势。实验推断电解效率下降是由于电极表面被聚合物污染导致,这一现象对电解处理有机物种的系统控制过程具有重要意义。     

职业接触苯乙烯工人静脉血中蛋白质环氧苯乙烯加合物的分析测定

静脉血中蛋白质－环氧苯乙烯（ＳＯ）加合物的分析测定是将蛋白质中半胱氨酸残留经分解后，用Ｒａｎｅｙ Ｎｉ催化反应生成两种加合物：α－苯己醇，β－苯已醇，再用五氟苯氯衍生，ＧＣ／ＭＳ测定，用同样的方法测ＳＤ大鼠血的蛋白质加合物，结果表明动物血中蛋白质加的与实验的苯乙烯或ＳＯ剂量有较好的相关性；而且ＳＯ与半胱氨酸的反应α位强于β位，在人群实验中，对一个石棉厂职业接触苯乙烯工人静脉血中的蛋白质加合物进行测     

伊春河河水水溶性腐殖酸内源释放模型

以水溶性腐殖酸含量很高的伊春河为例，利用冬季冰封无外源输入的条件，在有产室内模拟研究的基础上，通过现场采样及测定，建立了伊春河河水水溶性腐殖酸的内源释放模型，根据同期采集样品进行的验证表明，该模型能够准确地反映河流沉积物中水溶性瘁殖酸向河水中释放的速率以及速率与流速等条件的定量关系。     

我国不锈钢制品与铝制品行业进展与趋势

对不锈钢制品和铝制品行业的进展进行了分析 ,并对其发展趋势进行了预测     

Enhanced removal of lead(II) and cadmium(II) from water in alum coagulation by ferrate(VI) pretreatment.

A laboratory study demonstrated that ferrate pretreatment significantly enhanced lead and cadmium removal in alum coagulation, under the conditions of natural surface water. The enhancement of lead removal was approximately 21 to 37% by ferrate pretreatment at a dosage of 1 to 5 mg/L. The enhanced removal of cadmium by ferrate pretreatment at a dosage of 1 to 5 mg/L exceeded the removal by alum coagulation alone 2-to 12-fold. Cadmium is much more difficult to remove than lead in alum coagulation. The performance of ferrate in enhancing the removal of lead and cadmium in alum coagulation was better than that of ferric chloride. The removal of lead and cadmium was highly pH-dependent, following the general trend of higher pH being related to higher removal. Satisfactory removal of cadmium could be expected by ferrate pretreatment combined with adjusting the pH of the water.     

Influence of hydrogeochemical processes on zero-valent iron reactive barrier performance: a field investigation

Geochemical and mineralogical changes were evaluated at a field Fe0-PRB at the Oak Ridge Y-12 site concerning operation performance during the treatment of U in high NO3- groundwater. In the 5-year study period, the Fe0 remained reactive as shown in pore-water monitoring data, where increases in pH and the removal of certain ionic species persisted. However, coring revealed varying degrees of cementation. After 3.8-year treatment, porosity reduction of up to 41.7% was obtained from mineralogical analysis on core samples collected at the upgradient gravel-Fe0 interface. Elsewhere, Fe0 filings were loose with some cementation. Fe0 corrosion and pore volume reduction at this site are more severe due to the presence of NO3- at a high level. Tracer tests indicate that hydraulic performance deteriorated: the flow distribution was heterogeneous and under the influence of interfacial cementation a large portion of water was diverted around the Fe0 and transported outside the PRB. Based on the equilibrium reductions of NO3- and SO4(2-) by Fe0 and mineral precipitation, geochemical modeling predicted a maximum of 49% porosity loss for 5 years of operation. Additionally, modeling showed a spatial distribution of mineral precipitate volumes, with the maximum advancing from the interface toward downgradient with time. This study suggests that water quality monitoring, coupled with hydraulic monitoring and geochemical modeling, can provide a low-cost method for assessing PRB performance.     

Influence of hydrogeochemical processes on zero-valent iron reactive barrier performance: a field investigation

Geochemical and mineralogical changes were evaluated at a field Fe0-PRB at the Oak Ridge Y-12 site concerning operation performance during the treatment of U in high NO3- groundwater. In the 5-yr study period, the Fe0 remained reactive as shown in pore water monitoring data, where increases in pH and the removal of certain ionic species persisted. However, coring revealed varying degrees of cementation. After 3.8-yr treatment, porosity reduction of up to 41.7% was obtained from mineralogical analysis on core samples collected at the upgradient gravel-Fe0 interface. Elsewhere, Fe0 filings were loose with some cementation. Fe0 corrosion and pore volume reduction at this site are more severe due to the presence of NO3- at a high level. Tracer tests indicate that hydraulic performance deteriorated: the flow distribution was heterogeneous and under the influence of interfacial cementation a large portion of water was diverted around the Fe0 and transported outside the PRB. Based on the equilibrium reductions of NO3- and SO4(2-) by Fe0 and mineral precipitation, geochemical modeling predicted a maximum of 49% porosity loss for 5 yr of operation. Additionally, modeling showed a spatial distribution of mineral precipitate volumes, with the maximum advancing from the interface toward downgradient with time. This study suggests that water quality monitoring, coupled with hydraulic monitoring and geochemical modeling, can provide a low-cost method for assessing PRB performance.