对秦皇岛港西港搬迁改造工程的绿色思考

秦皇岛港西港搬迁改造工程对完善港口功能,振兴临港产业,缓解城市污染,促进港城互动,建设美丽港城,具有重要历史意义。针对搬迁改造工程中存在的问题与不足,提出应进一步完善搬迁改造规划,加大环保力度,从秦皇岛港口规划、布局到建设、生产,全面落实《绿色港口评价等级标准》,将改造工程对环境的负面影响降到最低,全力将秦皇岛港建设成为绿色港口。     

不同溶剂和反应温度对污泥热液化制取生物质油性质影响研究

选取4种溶剂(水、乙醇、正己烷、水-乙醇共溶济)作为污泥热液化制取生物质油的溶剂,分析溶剂种类和反应温度对热液化效果和生物质油性质的影响.结果表明:相同温度下,生物质油产率随溶剂种类变化趋势为:乙醇水-乙醇共溶剂正己烷水,最高产率为54.82%(乙醇溶剂,240℃).污泥有机物转化率随溶剂种类变化趋势为:水-乙醇共溶剂乙醇水正己烷,最高有机物转化率为96.40%(水-乙醇共溶剂,330℃).污泥经热液化处理后,碳、氢、氮、硫元素在生物质油中富集,氧含量下降,热值36 MJ·kg-1(乙醇、240℃除外).不同溶剂油成分差别较大,采用水或正己烷,产物主要是脂肪酸类、烷烃及部分酰胺和腈类,采用乙醇或水-乙醇共溶剂,产物主要是酯类、烷烃类.生物质油沸点集中分布在250~500℃,添加乙醇溶剂可显著提高生物质油轻组分含量.     

有机溶剂中温法溶出光伏组件封装材料乙烯-醋酸乙烯酯

采用有机溶剂邻二氯苯中温法溶出模拟光伏组件的封装材料乙烯-醋酸乙烯酯(EVA),探究了不同条件下EVA的溶出率及模拟组件的分离率,通过正交实验确定了有机溶剂中温法处理EVA的最佳条件.实验结果表明,在反应温度160℃、固液比(光伏组件个数与邻二氯苯体积之比,个/mL)4:100、搅拌转速800 r/min、反应时间24...     

加速溶剂萃取-固相萃取-高效液相色谱/三重四级杆质谱法测定土壤中6种喹诺酮类抗生素残留

为测定污染土壤中的6种低残留喹诺酮类抗生素(氧氟沙星、培氟沙星、恩诺沙星、环丙沙星、诺氟沙星、恶喹酸),全面优化了一种联合加速溶剂萃取(ASE)、固相萃取(SPE)和高效液相色谱/三重四级杆质谱(HPLC/MSMS)3种检测技术的分析方法.样品采用甲醇和0.1 mol/L EDTA-McIlvaine缓冲液(1∶1)进...     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.     

上海与伦敦城市绿地的生态功能及管理对策比较研究

在资料收集及实地采样调查的基础上 ,文章对上海与伦敦城市绿地的生态功能及管理对策进行了比较分析 ,指出了上海城市绿地建设及管理中的一些优点及不足之处。     

柚园间种作物及施用不同有机肥对土壤与柚果的影响

柚树间种短期经济作物在提高柚园经济效益的同时,还可提高土壤的有机质和N、P、K养分质量分数,改善柚园小区气候,增加有机肥来源。间种物残余体作为绿肥,可显著地提高柚果产量和质量。     

加速溶剂同时萃取和净化-气相色谱-三重四极杆串联质谱测定土壤和沉积物中8种多溴联苯醚

建立了土壤和沉积物中8种多溴联苯醚(PBDEs,BDE-28、BDE-47、BDE-99、BDE-100、BDE-153、BDE-154、BDE-183和BDE-209)加速溶剂同时萃取和净化-气相色谱-三重四极杆串联质谱(ASE-GC-MS-MS)的分析方法。通过优化加速溶剂萃取与弗罗里硅土在线净化和串联质谱多反应监测模式的条件,较好地去除基质干扰,并提高了三重四极杆串联质谱定性的准确性及定量的灵敏性。该方法采用改进的色谱柱能同时分析包括高溴代联苯醚BDE-209在内的8种PBDEs,其浓度范围为1～100 ng/mL(BDE-209为10～1 000 ng/mL),线性良好,线性回归系数均大于0.997。方法检出限为0.004～0.1 ng/g,方法回收率为75%～110%,方法精密度为2.4%～15.6%。适于批量处理土壤和沉积物中含有多组分痕量PBDEs的样品。     

郑州市土壤与绿色植物中汞的分布特征

汞污染具有生物积累性,因而得到社会广泛关注。研究监测和评估了郑州市城区土壤和绿色植物叶片中汞浓度、分布、污染水平等。研究发现郑州市主城区土壤总汞浓度为0. 150～0. 958 mg/kg,平均浓度为0. 448 mg/kg;郑州市主城区绿色植物叶片总汞浓度为0. 017～0. 249 mg/kg,平均浓度为0. 107 mg/kg;土壤和叶片中汞浓度按功能区排序为交通枢纽区工业区商业区行政区高教区住宅区。采用地累积指数法对郑州市80个土壤样品的汞污染水平进行评估,结果显示60%受到轻度污染,35%受到偏中度污染,5%受到中度污染。研究较为全面地分析了土壤汞污染的现状及浓度,为郑州市土壤汞污染防治提供参考。     

ASE-气相色谱法测定油田区土壤中多种石油烃

采用气相色谱法测定油田区土壤中C_(10)～C_(40)的石油烃,通过优化加速溶剂萃取的条件,使方法在62 mg/L～3 100 mg/L范围内线性良好,方法检出限为4.8 mg/kg。用该方法测定石油区短期、中期、长期油井污染土壤样品,5次测定结果的RSD为1.3%～5.2%,加标回收率为84.8%～98.5%,有证标准样品测定结果在可信区间内。