石墨相氮化碳协同UV-H_2O_2光催化降解亚甲基蓝

以三聚氰胺为前驱体,经热解—回流法制备了石墨相氮化碳(g-C3N4),采用XRD、FTIR、SEM、EDS、PL等技术对g-C_3N_4进行了表征。研究了g-C_3N_4在UV-H_2O_2体系中对废水中亚甲基蓝(MB)的光降解效果。实验结果表明,UV+g-C_3N_4催化剂+H_2O_2体系能协同降解MB,在初始MB质量浓度为20 mg/L、初始废水p H为5、废水体积为250 mL、g-C_3N_4加入量为0.10 g、H_2O_2浓度为0.4 mmol/L、反应温度为25℃的优化工艺条件下,紫外光照射70 min时MB脱色率达98.32%。g-C_3N_4催化剂具有较好的重复使用性能,使用5次后MB脱色率仍保持在95.10%。     

由粉煤灰合成单一的沸石及其对Cr(Ⅵ)的吸附研究

以粉煤厌为原料采用两步法合成了2种单一沸石矿物种的NaA和NaX型沸石,并对产物的结构和性能进行了详细表征.2种沸石产物的吸附性能比较结果表明,NaA型沸石优于NaX型沸石.在静态吸附条件下,研究了NaA型沸石吸附水溶液中Cr(Ⅵ)的相关参数(溶液pH值、吸附温度和吸附时间),并用Langmuir和Freundlich等温吸附线对吸附结果进行拟和.结果表明:Cr(Ⅵ)的吸附行为符合Langmuir方程;饱和吸附量为47.78 mg/g.NaA型沸石对Cr(Ⅵ)的吸附是物理和化学吸附两种行为共同作用的结果.     

Assessment of leaching behavior and human bioaccessibility of rare earth elements in typical hospital waste incineration ash in China

Leaching behavior and gastrointestinal bioaccessibility of rare earth elements (REEs) from hospital waste incineration (HWI) fly and bottom ash samples collected from Beijing and Nanjing Cities were assessed. In the same ash sample, the leaching concentrations of individual REEs determined by the Toxicity Characteristic Leaching Procedure (TCLP) were higher than those detected by the European standard protocol (EN-type test), thereby suggesting that the low pH value of leaching solution was an important factor influencing the leachability of REE. The REE bioaccessibility results, which were evaluated using the physiologically based extraction test (PBET), indicated that REEs were highly absorbed during gastric phase by dissolution; and subsequently precipitated and/or re-adsorbed in small intestinal phase. The relative amounts of the total REEs extracted by the TCLP method, EN-type test and PBET test were compared. In addition to the pH value of extraction solutions, the chelating role of REEs with organic ligands used in the PBET method was also an important parameter affecting REE adsorption in human body. Additionally, this study showed that REEs were extracted by these methods as concomitants of heavy metals and anions (NO₃ ^–, F^–, SO₄ ^2–, and Cl^–) from HWI ash, which probably caused the remarkably complex toxicity on human body by the exposure pathway.

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同源地人工湖水体和底泥中有机物组成及有机结构的分析研究

采用XAD-8大孔吸附树脂对水体和底泥中的有机物进行组分分离,并通过傅里叶变换红外光谱(FTIR)、紫外-可见光谱(UV-Vis)和三维荧光光谱(3DEEMs)对自然水体和底泥中的疏水酸(腐殖酸、富里酸)、疏水碱、疏水中性物质和亲水物质进行表征和对比.结果表明,水体中有机物含量:亲水物质富里酸腐殖酸疏水碱疏水中性物质,底泥中有机物的含量为:腐殖酸富里酸亲水物质疏水碱疏水中性物质.根据红外、紫外、三维荧光光谱可知底泥中有机物的芳香程度、不饱和程度及分子量大小略高于水体有机物.根据荧光指数(FI)和自生源指标(BIX)可知,底泥和水体的腐殖酸和富里酸主要来源于陆生动植物和土壤有机质,而其余物质主要源于细菌和藻类活动.     

美国公共管理面面观——在伊利诺伊州芝加哥市感受美国

美国政府的公共管理是建立在美国特有的政治制度和经济体制的基础上的。 美国的政府体系是由联邦、州和地方政府三个层级组成的联邦制政府体系，它们分别具有各自独立的政府权威和管辖领域．实行多中心治理和法定分权体制。联邦政府由立法机构、行政机构和司法机构三个分支组成，实行三权分立的政治体制。     

载钯螯合树脂的制备、表征及其降解多溴联苯醚的初步研究

以聚丙烯醛-异烟酰腙螯合树脂为高分子载体, 利用其活性基团对钯的选择性富集分离性能, 将金属元素钯键合到高分子载体上, 制备一种含钯树脂材料(树脂1), 并进一步原位还原得到还原态的载钯树脂(树脂2)。利用红外光谱、扫描电镜和X射线衍射等对以上2种含钯树脂材料进行了分析表征，并考察了它们对持久性有机污染物(POPs)多溴联苯醚(PBDEs)的脱溴降解性能。结果表明,2种树脂对BDE₂₀₉均有降解活性， 其中树脂1的降解性能比树脂2的降解性能要高， 树脂中钯的氧化形态可能对BDE₂₀₉的催化降解起主要作用。     

脱硫石膏粒径分布与脱水性能实验研究

脱硫石膏粒径分布是影响脱硫石膏浆液脱水性能的重要因素之一，以干法、湿法筛分和研磨破碎获得不同粒径分布的脱硫石膏，在相同的过滤条件下，对不同粒径分布脱硫石膏浆液脱水性能进行了研究，实验结果表明，当脱硫石膏粒径d50大于50μm且（d90-d10）小于100μm，真空过滤最大真空度不低于0．098MPa，过滤时间不少于2．5min，滤饼厚度不超过20mm时，石膏滤饼含水率可以降低到12％以下（最低可达10％）；d50在17μm为脱硫石膏在相同的过滤条件下能够实现真空脱水干燥的转折点；d50和（d90-d10）共同影响石膏脱水性能，d50小于20μm时，仅表现为d50的影响。     

碱熔融法合成NaA和NaX型粉煤灰沸石的品质表征

以粉煤灰为原料采用碱熔融法合成了2种单一沸石矿物种的NaA和NaX型沸石,并对产物的结构、性能和应用指标进行了详细表征.经x射线衍射和IR光谱分析,表明合成产物是无杂晶生成的NaA和NaX型沸石相;在扫描电镜观察下,产物分别具有NaA和NaX型沸石的立方体和八面体晶体骨架结构.DTA分析表明了合成产物中沸石水的存在,且产物热稳定性较好.通过对比,粉煤灰合成的NaA和NaX型沸石的比表面积达到了相应商品沸石的66.9%和83.6%;孔容为41.1%和70.2%;阳离子交换容量(CEC,cation exchange capacity)为82.93%和84.31%.通过比较化学组成表明,大规模应用合成产物不会对环境造成危害.     

臭氧-BAF组合工艺对石化行业废水深度处理的中试研究

采用臭氧-曝气生物滤池（BAF）组合工艺对中石化九江分公司二级生化出水进行深度处理中试实验。探讨了臭氧投加量、进水水质冲击负荷等因素对该组合工艺出水COD、NH₄⁺-N的影响。中试结果表明，在该水质条件下，臭氧最佳投加量为20~25 mg/L；组合工艺处理后出水COD低于40 mg/L，NH₄⁺-N低于5 mg/L，达到中水回用设计标准；该组合工艺能够经受一定冲击负荷。     

Distribution,source, and environmental risk assessment of phthalate esters (PAEs) in water,suspended particulate matter,and sediment of a typical Yangtze River Delta City,China

Phthalates (PAEs) in drinking water sources such as the Yangtze River in developing countries had aroused widespread concern. Here, the water, suspended particulate matter (SPM), and sediment samples were collected from 15 sites in wet and dry seasons in Zhenjiang, for the determination of six PAEs (DMP, DEP, DIBP, DBP, DEHP, and DOP) using the solid-phase extraction (SPE) or ultrasonic extraction coupled with gas chromatography-mass spectrometry (GC-MS). The total concentrations of six PAEs (Σ₆PAEs) spanned a range of 2.65–39.31 μg L^?1 in water, 1.97–34.10 μg g^?1 in SPM, and 0.93–34.70 μg g^?1 in sediment. The partition coefficients (K_d1) of PAEs in water and SPM phase ranged from 0.004 to 3.36 L g^?1 in the wet season and from 0.12 to 2.84 L g^?1 in the dry season. K_d2 of PAEs in water and sediment phase was 0.001–9.75 L g^?1 in the wet season and 0.006–8.05 L g^?1 in the dry season. The dominant PAEs were DIBP, DBP, and DEHP in water and SPM, DIBP, DEHP, and DOP in sediment. The concentration of DBP in water exceeded the China Surface Water Standard. The discharge of domestic sewage and industrial wastewater might be the main potential sources of PAEs. The risk quotient (RQ) method used for the risk assessment revealed that DBP (0.01 < RQ < 1) posed a medium risk, while DIBP and DEHP (RQ > 1) posed a high environmental risk in water, DIBP (RQ > 1) also showed a high risk in sediment.