Effects of Meteorological Parameters on Air Pollutant Concentrations in Elazig,Turkey

In the present study, air pollutant concentrations have been analyzed statistically with meteorological factors in the city of Elazig, which is located in the east Anatolia region of Turkey, for the months of September, October, November, December, January, February, March, and April during the years 2003 and 2004. SPSS code was used for statistical analyses. The relationship between monitored air pollutant concentrations, such as SO₂ and the total suspended particles (TSP) data, and meteorological factors such as wind speed, temperature, relative humidity and pressure was investigated. According to the results of linear and non-linear regression analysis, it was found that there is a moderate and weak level of relation between the air pollutant concentrations and the meteorological factors in Elazig. The correlation between the previous day's SO₂, TSP concentrations and actual concentrations of these pollutants on that day was investigated and the coefficient of determination R was found to be 0.80 and 0.76, respectively. The statistical models of SO₂ and TSP, including all of the meteorological parameters, gave an R of 0.50 and 0.40, respectively. Further, in order to develop this model, the previous day's SO₂ and TSP concentrations were added to the equations. The new model for SO₂ and TSP was improved considerably with R = 0.85 and 0.80, respectively.     

Monitoring total suspended solids by using nephelometry

Correlation curves were developed relating nephelometric turbidity units (NTU) with total suspended solids (TSS) for diked upland dredged material placement site effluents of three US Army Corps of Engineers (COE) maintenance dredging projects in the Chesapeake Bay, Maryland. The procedure was developed in an effort to ensure compliance with Maryland's 400 milligrams per liter (mg/l) TSS standard for COE dredging projects. Samples of the sediments to be dredged were collected and analyzed, correlating turbidity readings with TSS determined by standard gravimetric techniques. The correlation curves were provided to the COE inspectors to measure the effluent with a turbidity meter and to extract a TSS concentration from the correlation curve. Samples collected and analyzed after initiation of the dredging indicated that the correlation curves were an overestimate of the actual TSS concentrations of the effluent discharges. The procedure, endorsed by the State of Maryland, provided immediate on-site TSS analysis eliminating the previously encountered delays in obtaining gravimetric analysis of effluent discharges and potential contract management problems.     

流动注射分析法测定水中的总磷

应用LACHATQC8500型三通道流动注射分析仪,采用过硫酸钾在线紫外消解不同形态的磷,使其转化为磷酸盐。正磷酸盐与钼酸铵和酒石酸锑钾反应,生成磷钼化合物。此磷钼化合物被抗坏血酸还原,形成蓝色化合物,它在880nm处有吸收。仪器检出限为0.0012mg/L,线性范围为0.05～1mg/L(r>0.9990),加标回收率为95.0%～104%。与GB11893-89钼酸铵分光光度法比较,其结果无显著差异。实验结果表明,该方法简便、快速、准确,适用于水中总磷的测定。     

总铬分析前处理方法的改进探讨

采用密塞高压蒸汽法代替锥形瓶,加热氧化法测定总铬,缩短了分析时间,操作简便,分析结果精密度高、准确度好。     

Application of ferrate（VI） in the treatment of industrial wastes containing metal-complexed cyanides ： A green treatment

Ferrate(VI) was employed for the oxidation of cyanide (CN) and simultaneous removal of copper or nickel in the mixed/complexed systems of CN-Cu, CN-Ni, or CN-Cu-Ni. The degradation of CN (1.00 mmol/L) and removal of Cu (0.095 mmol/L) were investigated as a function of Fe(VI) doses from 0.3–2.00 mmol/L at pH 10.0. It was found that Fe(VI) could readily oxidize CN and the reduction of Fe(VI) into Fe(III) might serve e ciently for the removal of free copper ions. The increase in Fe(VI) dose apparently favoured the CN oxidation as well as Cu removal. Moreover, the pH dependence study (pH 10.0–13.0) revealed that the oxidation of CN was almost una ected in the studied pH range (10.0–13.0), however, the maximum removal e ciency of Cu was obtained at pH 13.0. Similarly, treatment was carried out for CN-Ni system having the initial Ni concentration of 0.170 mmol/L and CN concentration of 1.00 mmol with Fe(VI) dose 2.00 mmol at various pH values (10.0–12.0). Results showed a partial oxidation of CN and partial removal of Ni. It can be observed that Fe(VI) can partially degrade the CN-Ni complex in this pH range. Further, Fe(VI) was applied for the treatment of simulated industrial waste/e uent waters treatment containing CN, Cu, and Ni.     

Distribution of PBDEs in air particles from an electronic waste recycling site compared with Guangzhou and Hong Kong, South China

Air samples of total suspended particles (TSP, particles less than 30-60 microm), and particles with aerodynamic diameter smaller than 2.5 microm (PM(2.5)) were collected simultaneously at Guiyu (an electronic waste recycling site), three urban sites in Hong Kong and two urban sites in Guangzhou, South China from 16 August to 17 September 2004. Twenty-two PBDE congeners (BDE-3, -7, -15, -17, -28, -49, -71, -47, -66, -77, -100, -119, -99, -85, -126, -154, -153, -138, -156, -184, -183, -191) in TSP and PM(2.5) were measured. The results showed that the overall average concentrations of TSP and PM(2.5) collected at Guiyu were 124 and 62.1 microg m(-3), respectively. The monthly concentrations of the sum of 22 BDE congeners contained in TSP and PM(2.5) at Guiyu were 21.5 and 16.6 ng m(-3), with 74.5 and 84.3%, contributed by nine congeners (BDE-28, -47, -66, -100, -99, -154, -153, -183 and -191 respectively). This pattern was similar to Tsuen Wan site of Hong Kong. Two urban sites of Guangzhou had the same congener pattern, but were different from Yuen Long and Hok Tsui sites of Hong Kong. The results also showed that the amount of mono to penta brominated congeners, which are more toxic, accounted for 79.4-95.6% of Sigma(22)PBDEs from all sites. All congeners tested in Guiyu were up to 58-691 times higher than the other urban sites and more than 100 times higher than other studies reported elsewhere. The higher concentration in the air was due to heating or opening burning of electronic waste since PBDEs are formed when plastics containing brominated flame retardants are heated.     

Intake of phthalates and di(2-ethylhexyl)adipate: results of the Integrated Exposure Assessment Survey based on duplicate diet samples and biomonitoring data

Phthalates are ubiquitous environmental chemicals with potential detrimental health effects. The purpose of our study was to quantify dietary intake of phthalates and of DEHA (Di-ethylhexyl adipate) using duplicate diet samples and to compare these data with the calculated data based on urinary levels of primary and secondary phthalate metabolites. 27 female and 23 male healthy subjects aged 14-60 years collected daily duplicate diet samples over 7 consecutive days. Overall, 11 phthalates were measured in the duplicates by GC/MS and LC/MS methods. Urinary levels of primary and secondary phthalate metabolites are also available. The median (95th percentile) daily intake via food was 2.4 (4.0) microg/kg b.w. (Di-2-ethylhexyl phthalate, DEHP), 0.3 (1.4) microg/kg b.w. (Di-n-butyl phthalate, DnBP), 0.6 (2.1) microg/kg b.w. (Di-isobutyl phthalate, DiBP) and 0.7 (2.2) microg/kg b.w. for DEHA. MEPH (Mono-2-ethylhexyl phthalate) was detectable only in minor concentrations in the samples, thus conversion of DEHP to MEHP and dietary intake of MEHP were negligible. When comparing back-calculated intake data of the DEHP metabolites with dietary DEHP intake from the day before significant correlations were observed for most of the metabolites. No correlation was found for DnBP and only a weak but significant correlation for DiBP. The median and 95th percentile daily dietary intake of all target analytes did not exceed the recommended tolerable daily intake. Our data indicated that food was the predominant intake source of DEHP, whilst other sources considerably contributed to the daily intake of DnBP and DiBP in an adult population.     

水中总碱度测定的不确定度评定

以水中总碱度为例,分析了测试过程中不确定度的来源,对各不确定度分量进行评定及合成,并计算得出合成不确定度和扩展不确定度。结果表明,对本测试方法影响较大的不确定度分量是标准物质配制、溶液体积引入和标定过程中的随机因素。在样品重复测定的条件下,测定结果的不确定度仅与溶液中的质量浓度有关。     

环境样品保存过程中氮的转化规律

通过对环境样品保存过程中NH3-N、NO2-N、NO3-N及总氮的测定来研究水样中氮转化规律,找出三氯在一定条件下相互转化规律关系,提高环境样品中三个分析项目的分析准确性,正确反应环境样品中的真实情况。对于认识水体中氮的循环,防止水体污染,保护水域环境,充分利用开发水资源有着十分重要的意义。     

Implementing service-based chemical procurement: lessons and results

Chemical use reduction is strongly desirable for environmental and public welfare reasons, and is a critical element of moving towards more sustainable consumption in the business-to-business economy. However, the fundamental economic relationship between chemical supplier and chemical customer creates supply side incentives for increased chemical use. Chemical management services (CMS) is a business model that aligns economic incentives in the chemical supplier–customer relationship towards reduced chemical use by making chemical services rather than chemical volume the basis of supplier compensation. CMS thus ‘servicizes’ the chemical supply chain and is a Product Service System with significant potential environmental benefits. CMS enjoys high penetration in the US auto and semiconductor sectors, and is emergent in other sectors. The paper synthesizes lessons learned from hands-on work with 15 chemical-using firms over 5 years in all aspects of CMS program implementation. Key points are that poor cost accounting and chemical information management form significant barriers to making, understanding and evaluating the CMS business case. The details of contractual compensation mechanisms are critical to achieving in practice the potential environmental benefits of the CMS model.