粉煤灰吸附—石灰沉淀处理高浓度含氟废水

采用粉煤灰吸附—石灰沉淀处理高浓度含氟废水.正交实验得到的最佳工艺条件为:反应温度10℃,石灰加入量3.0 g/mL,反应时间60 min,废水pH 6.88.在此最佳工艺条件下处理F质量浓度为150 mg/L的含氟废水,Fˉ去除率为97.53％.Mn2+,Fe3+,Mg2+,A13+,Zn2+单独存在时,随5种阳离子质量浓度增大,Fˉ去除率略有增加;当5种阳离子共同存在且质量浓度均大于500 mg/L时,Fˉ去除率下降.PO43-,SO42-,CO32-,NO3-单独存在时对Fˉ去除率影响不大;当4种阴离子共同存在且质量浓度均大于800 mg/L时,Fˉ去除率低于对照实验.     

粉煤灰基吸附剂对模拟废水中Cd2+的吸附性能

以粉煤灰为原料、Na2CO3为助熔剂,采用盐熔融—水浴结晶法制备粉煤灰基吸附剂。探讨了吸附剂的最佳制备条件及其对模拟废水中Cd2+的最佳吸附条件、吸附动力学和吸附机理。实验结果表明:制备吸附剂的最佳工艺条件为m(粉煤灰)∶m(Na2CO3)为1∶2,焙烧温度为450℃;采用最佳制备工艺条件下制备的吸附剂(记作2-450℃-FA吸附剂),在初始Cd2+质量浓度为300 mg/L、初始溶液pH为7.7、振荡时间为120 min的条件下,对模拟废水中Cd2+的去除率为98.0%。2-450℃-FA吸附剂对Cd2+的吸附主要受颗粒内扩散控制,吸附过程可用准二级吸附动力学方程很好地描述。Ea为77.22 kJ/mol,吸附过程主要为化学吸附。     

电渗析技术及其应用

电渗析技术是膜分离技术之一,具有低能耗,高效率,连续运行、环境友好等显著优点,在多个行业中有着广泛的使用。简述了几种常见的电渗析技术,包括填充床电渗析,倒极电渗析和双膜电渗析等,着重介绍了电渗析技术在水处理、食品和化工方面的应用,并简单探讨了电渗析技术其发展前景。     

硝酸及氯离子对高温硝酸铵水溶液热危险性的影响研究

国内外学者对硝酸铵的危险性进行了大量的研究,而对其水溶液的危险性至今开展不多。笔者采用差示扫描量热仪(DSC)及全自动反应量热仪(RC1e)对高温状态下的硝酸铵水溶液的热分解危险性、杂质离子对其稳定性的影响进行了研究。纯硝酸铵和90%硝酸铵水溶液的DSC实验表明,90%硝酸铵溶液和分析纯硝酸铵具有相似的热爆炸危险;90%硝酸铵水溶液在140~180℃之间的RC1e试验表明:硝酸或氯离子单独存在时,对硝酸铵分解都有不同程度的抑制作用,而同时存在时则大大降低体系的热稳定性。该结果对保障硝酸铵在生产、使用过程中的安全具有重要的参考价值。     

金属有机骨架材料UiO-66的制备及其对溶液中NO_3~-的吸附

采用溶剂热法合成了金属有机骨架材料UiO-66。通过XRD、SEM、FTIR对其进行了表征。考察了UiO-66对溶液中NO_3~-的吸附性能。实验结果表明,加入冰乙酸作调节剂后,得到的UiO-66晶体形貌均匀,直径在100nm左右,结晶度更好。在初始溶液pH为5、反应温度为30℃的条件下,UiO-66吸附NO_3~-反应90 min后,吸附达到平衡,平衡吸附量为39.67 mg/g。UiO-66吸附NO_3~-的吸附行为符合Freundlich等温线和准二级动力学吸附模型。吸附作用主要是材料中金属位点Zr对NO_3~-的静电吸附。UiO-66材料具有良好的再生性能,可重复使用。     

机掘工作面有效通风及其评价指标研究

就评价机掘工作面的有效通风提出了空气年龄、空气品质、换气效率、排污效率等概念,并分析给出了其指标的计算模型。有效通风指标不仅与空气年龄有关,而且与掘进工作面通风气流组织、污染物浓度及分布特性有关。提高机掘工作面空气品质,除了要提高换气排污效率外,还应有效地组织掘进工作面的通风气流     

Potential application of 2-(6-ethylamino-3-ethylimino-2,7-dimethyl-3H-xanthen-9-yl) benzoic acid phenyl thiourea for mercury determination

Heavy metal contamination of the environment is a public health problem and research to develop new tools for monitoring the environmental impact of these elements is necessary. This study describes the preparation of a rhodamine-based probe 1 and its potential applications for detecting mercuric ion [Hg(II)] in samples from a nutrition media containing Salvinia auriculata. It was observed that an excess of probe 1 led to quenching in the fluorescence/absorption response, which was evidenced by a decrease in the signal when the stoichiometry differed from 1:1. Consequently, this probe is not suitable for quantitative analysis of Hg(II). Also, probe 1 reacts with methylmercury (MeHg) with different stoichiometry than that observed for Hg(II). These results indicate the potential application of probe 1 for qualitative detection of Hg(II) and MeHg in environmental samples.     

Assessment of methane from agricultural field during the entire paddy cropping seasons – a case study

A systematic effort was made to assess the emission of methane from paddy fields using closed chamber technique. Methane emission measurements were performed over a year during the Kharif (wet season), Rabi (dry season), and fallow periods. Various soil parameters like redox potential, organic carbon and ferrous ion were determined to evaluate their control on methane emissions. Diurnal measurement of the flux showed a minimum (0.44?mg?m^?2?h^?1) in the morning (8?a.m.), which increased gradually to a value of 1.16?mg?m^?2?h^?1 till the evening due to the rise in soil temperature. The seasonally integrated flux (E _SIF) for CH₄ was calculated. The E _SIF for methane during Kharif and Rabi crops were found to be 5.97?g?m^?2 and 2.59?g?m^?2, respectively. It was observed that the methane flux was maximum during flowering and fertilizer application stages for both paddy cropping seasons. The redox potential was low and the ferrous ion was higher during flowering and tiller stages. The methane emission was higher at E _AIF) was calculated for methane to make a budget estimate of methane emission from rice cultivated under rain fed drought prone water regime.     

Effect of dissolved organic matter on nitrate-nitrogen removal by anion exchange resin and kinetics studies

The effects of dissolved organic matter (DOM) on the removal of nitrate-nitrogen from the model contaminated water have been investigated utilizing the strong base anion exchange resins. With the increase of gallic acid concentration from 0 to 400 mg/L, the adsorption amount of nitrate-nitrogen on the commercial resins, including D201, Purolite A 300 (A300) and Purolite A 520E (A520E), would significantly decrease. However, the presence of tannin acid has little impact on nitrate-nitrogen adsorption on them. Compared to D201 and A300 resins, A520E resin exhibited more preferable adsorption ability toward nitrate-nitrogen in the presence of competing organic molecules, such as gallic acid and tannin acid at greater levels in aqueous solution. Attractively, the equilibrium data showed that the adsorption isotherm of nitrate-nitrogen on A520E resin was in good agreement with Langmuir and Freundlich equations. The rate parameters for the intra particle diffusion have been estimated for the different initial concentrations. In batch adsorption processes, nitrate-nitrogen diffuse in porous adsorbent and rate process usually depends on t 1/2 rather than the contact time. The pseudo first- and the second-order kinetic models fit better for nitrate-nitrogen adsorption onto A520E resin. The observations reported herein illustrated that A520E resin will be an excellent adsorbent for enhanced removal of nitrate-nitrogen from contaminated groundwater.