Effect of copper and cadmium on carbon assimilation and uptake of metals by algae

Two species of blue green algae Spirulina platensis and Anacystis nidulans grown in artificial aqueous media were treated with Cu and Cd in concentrations of 0.01, 0.1, 1.0 and 10 ppm to study carbon assimilation and Chlorophyll (Chl) A content. The species were treated with concentrations of 0.1, 0.5, 1.0, 5.0 and 10.0 ppm to study the uptake of metals with exposure time. Carbon assimilation and Chl A content showed responses proportional to the concentration in the general form y = K + n ln C, where C is the concentration of metal in ppm, while in case of uptake the relation was y = KC”; (where C is the molar concentration x 10^‐6 of the metal). The n values in case of uptake was found to be < 1 indicating a non‐Langmuir type of sorption. The concentration factors of metals decreased with metal concentration in the medium.     

Degradation of Carbofuran in Water by Solar Photocatalysis in Presence of Photosensitizers

The effect of the presence of photosensitizers, methylene blue (MB) and rose Bengal (RB), on the degradation of carbofuran (2,3-dihydro-2,2-dimethylbenzofuran-7-yl methylcarbamate) in water in a solar photocatalytic system was investigated. It was found that as compared to MB, RB generally showed a stronger effect on the decomposition of carbofuran under comparable conditions. Among the conditions studied, adding 2 × 10^?6 M of RB, that corresponding to 2% of the initial concentration of carbofuran solution in the system, rendered the most effective degradation of carbofuran. As a result, a carbofuran removal percentage of 69.9%, a mineralization efficiency of 28.0%, and a microtoxicity reduction of 65.0% could be achieved. The degradation and mineralization of carbofuran was found to follow the pseudo-first order reaction kinetics. The decomposition mechanism of carbofuran was further investigated through identification of the intermediates to elaborate the influence of dye photosensitizer on the solar photocatalysis of carbofuran in water. On the basis of the intermediates identified, including carbofuran phenol, 3-hydroxy carbofuran phenol, and substituted alcohols (3-phenoxy 1-propanol, 2-ethyl 1-hexanol, 2-butoxyl ethanol), it appears that hydrolysis and hydroxylation were the two key mechanisms for decomposing carbofuran during the process of solar photocatalysis with the aid of dye photosensitizer.     

紫外分光光度法测定污水COD值的误差分析研究

针对紫外分光光度法测定污水COD值的误差分析问题,给出了实验的仪器和试剂的配制方法,如测试主要仪器设备和主要试剂的配制,介绍了测定水样的采集地点,介绍了重铬酸钾法的测定原理及步骤,重铬酸钾法的测定原理和重铬酸钾法的测定步骤,紫外分光光度法的测定原理及步骤,如紫外分光光度法的测定原理和紫外分光光度法的测定步骤,并对结果进行了讨论,紫外分光光度法,标准曲线的确定,测定的结果比较和方法的准确度和精密度比较.     

碳纳米管负载纳米四氧化三铁多相类芬顿降解亚甲基蓝

在课题组前期研究的基础上,以碳纳米管(MWCNTs)为载体制备了Fe3O4/MWCNTs复合物并作为催化剂,以染料亚甲基蓝(MB)为降解对象,研究了该催化剂催化H2O2对亚甲基蓝溶液的降解特性及其影响因素,并考察了催化剂的重复使用效果,探讨了催化反应的机理.结果表明,在pH值3~8的范围内,催化反应体系都能有效降解MB,最佳pH值为3.5.随着催化剂投量的增加,MB的降解率明显提高,500 mg·L-1催化剂投量条件下,MB的降解率最高.随着H2O2初始浓度的增加,MB的降解率增加,10 mmol·L-1时MB的降解率最高.溶液中共存的阴离子会降低MB的降解率.在最佳条件,即温度25℃、H2O2浓度10 mmol·L-1、催化剂浓度500 mg·L-1的条件下,0.20 mmol·L-1MB在30 min内的降解率达到99.1%.催化剂重复使用后仍然具有较好的催化活性,说明Fe3O4在MWCNTs表面负载比较牢固,催化剂具有反复使用的能力.催化反应机理是催化剂催化H2O2产生羟基自由基,高活性的羟基自由基氧化MB.     

“绿水”的多角度评估及其管理研究

传统的水资源评估和管理忽视了在粮食生产和维护生态系统等方面都具有重要作用的"绿水".本文引入绿水概念,并针对现有绿水评估研究中缺乏小尺度评估方法研究等问题,以碧流河上游地区为例,使用SWAT水文模型在小尺度建立了多角度评估绿水(包括绿水流和绿水贮存)的方法.并使用此方法估算得到了绿水量,绿水时空分布规律以及气候变化条件下绿水的响应规律,研究了引入绿水概念后传统水资源管理的重要革新内容.研究结果表明,使用SWAT水文模型评估流域绿水,是引入绿水概念后进行小尺度绿水评估的有效办法,值得在中国推广使用.绿水评估结果对水资源管理有重要的指导作用.绿水概念的引入为水资源的管理与决策提供了新的思路和更加科学的办法.     

流动注射分光光度法测定废水中挥发酚

基于４－氨基安替比林显色原理,采用流动注射技术,建立了炼油废水中挥发酚的快速测定方法。分析速率为每小时４０个试样,线性范围为０．７５－２３．０ｍｇ／Ｌ。对１．５０ｍｇ／Ｌ苯酚标准溶液连续测定１０次,相对标准偏差为２．８％。对炼油废水样,本法测定结果与标准方法无显著性差异。     

用分光光度法测定有机质的研究

在强酸性溶液中、165℃和催化剂作用的条件下,土壤中的有机碳被K2Cr2O7迅速氧化,而K2Cr2O7中的Cr6+还原成Cr3+,Cr3+在600nm波长上有特征吸收,其吸光度与有机碳的浓度成正比。根据吸光度可计算出土壤有机质的含量。实验证明试剂和工作曲线的斜率有很好的稳定性和重现性。分光光度法测定有机质快速、准确。     

COD分光光度法与标准方法对比实验

ＣＯＤｃｒ分光光度快速测定法具有简便，快速，节能，省试剂等优点。其测定结果与标准方法之间有良好的可比性，最低检测限为５．０ｍｇ／ｌ 。     

紫外分光光度法测定水中总氮的不确定度评定

运用测量不确度评定的基本方法和程序,分析影响紫外分光光度法测定总氮的不确定度的各种因素,建立数学模型,合成计算总氮的不确定度。     

氯磺酚偶氮硫代若丹宁光度法测定环境水样中的汞

研究了氯磺酚偶氮硫代若丹宁(HSCT)与汞的显色反应。在pH3 8的HAc-NaAc缓冲介质中,TritonX-100存在下,HSCT与汞反应生成2∶1稳定络合物,λmax=550nm,体系ε=8 46×104L·mol-1·cm-1。汞含量在0—1 5mg/L内符合比耳定律。方法可用于水样中痕量汞含量的测定。