Low-temperature CO oxidation over Au-doped 13X-type zeolite catalysts: preparation and catalytic activity

Au-supported 13X-type zeolite (Au/13X) was synthesized using a common deposition–precipitation (DP) method with a solution of sodium carbonate as a precipitate agent. Further testing was conducted to test for catalytic oxidation of CO. A study was conducted on the effects of different preparation conditions (i.e., chloroauric acid concentration, solution temperature, pH of solution, and calcinations temperature) on Au/13X for CO oxidation. In respect to the catalytic activity, the relationship between different the preparation conditions and gold particles in 13X zeolite was analyzed using X-ray diffraction, TEM and XPS. The activity of Au/13X catalysts in CO oxidation was dependent on the chloroauric acid concentration. From XRD results, a higher chloroauric acid concentration induced larger gold nanoparticles, which resulted in lower catalytic activity. Results revealed that higher temperatures induced higher Au loading, homogeneous deposit, and smaller gold clusters on the support of 13X, resulting in higher CO activity. Furthermore, a pH of 5 or 6 generated greater amounts of Au loading and smaller Au particles on 13X than at a pH of 8 or 9. This may be a result of an effective exchange between Au(OH)2Cl2- and Au(OH)₃Cl^- on specific surface sites of zeolite under the pH’s 5 and 6. The sample calcined at 300°C showed the highest activity, which may be due to the sample’s calcined at 200°C inability to decompose completely to metallic gold while the sample calcined at 400°C had larger particles of gold deposited on the support. It can be concluded from this study that Au/13X prepared from a gold solution with an initial chloroauric acid solution concentration of 1.5 × 10^-3 mol·L^-1 gold solution pH of 6, solution temperature of around 90°C, and a calcination temperature of 300°C provides optimum catalytic activity for CO oxidation.     

Leaching characteristics of bisphenol A from epoxy-resin pavement materials

We investigated the leaching characteristics of bisphenol A (BPA) from two kinds of epoxy-resin pavement materials, one containing epoxy resins (EPs) and the other containing epoxy-acrylate resins (EPAs). Both samples contained residual BPA monomer, at levels of 9.0?µg?g^?1 for the EP resin sample and 4.4?µg?g^?1 for the EPA resin sample. These amounts were larger than amounts previously measured for polycarbonate samples. The amount of BPA leached from the samples increased with temperature. The leaching of BPA from EP was more strongly affected by temperature than the leaching from EPA. The pH also affected the amount of leached BPA. The maximum leached amount was observed under alkaline conditions (pH 10.8) for both sample types. The amounts of BPA that might leach from pavement materials during 1?h of heavy rain were estimated to be 0.9?µg?m^?2 for EP and 3.5?µg?m^?2 for EPA. Our results indicate that EPs disposed of in waste landfills without any treatment may be a source of BPA in leachate at landfill sites.     

以缓释肥的形式回收污泥溶解液中磷的研究

以聚合硫酸铁(PFS)为絮凝剂,单宁酸为助凝剂回收污泥溶解液中的磷。研究结果表明:在铁盐投加量为160mg/L,pH为8,单宁酸投加量为10 mg/L条件下,磷酸盐的回收率可达到97.0%。单宁酸促进了混凝沉淀物中磷的释放,表明利用该方法回收磷作为缓释肥的可行性。将沉淀物作为缓释磷肥施用于土壤中能够明显促进黑麦草的生长。     

吸收液对中空纤维膜接触器回收尿液中氨氮的影响

采用中空纤维膜接触器（Hollow Fiber Membrane Contactor, HFMC）回收尿液中的氨氮,系统研究了吸收液类型（H₃PO₄、H₂SO₄和HNO₃）对氨回收效能、水蒸气的跨膜通量和所获液体肥料的影响.结果表明,使用H₂SO₄作为吸收液时氨氮回收效能最优,其次是H₃PO₄和HNO₃.当采用H₂SO₄为吸收液时,氨氮回收率、氨跨膜通量和传质系数分别为84.49%±0.01%、22.92 g·m^-2·h^-1和2.37×10^-6 m·s^-1.HNO₃的挥发性使其从吸收液侧反向跨膜至料液侧,导致氨跨膜传质驱动力变小;此外,NH₃和HNO₃会在膜孔中反应并生成NH₄NO₃气溶胶,增加氨在膜孔中的传质阻力,导致氨氮的回收效能降低.对采用不同吸收液时膜两侧的水的活度差和理论水通量进行了计算,结果表明,随着氨氮的不断跨膜吸收,膜两侧的活度差和水通量逐渐增大,实验结束时水通量分别为7.44×10^-2 kg·m^-2·h^-1（H₃PO₄）、9.06×10^-2 kg·m^-2·h^-1（H₂SO₄）和2.00×10^-2 kg·m^-2·h^-1（HNO₃）.肥料组分分析表明,以H₂SO₄和HNO₃为吸收液可以获得仅含N素的单一液体肥料,以H₃PO₄作吸收液可获得N-P复合肥,（NH₄）₂HPO₄和NH₄H₂PO₄所占的比例分别为88.33%和11.67%.     

河南鸡冠洞洞穴水对极端气候的响应及其控制因素研究

为揭示洞穴水地球化学动态的变化特征及其控制因素,从2009年10月至2013年12月对黄土高原东南缘河南西部栾川县鸡冠洞洞穴水的水化学指标进行了4个完整水文年的动态监测.结果表明:1鸡冠洞洞穴水的化学类型主要是HCO-3-Ca2+-Mg2+和HCO-3-Mg2+-Ca2+型,阴离子中HCO-3占80%以上,阳离子中Ca2+、Mg2+是优势离子,地下河常年处于溶蚀状态,池水、滴水处于沉积状态.2鸡冠洞洞穴滴水、池水可以很好地响应外部气候环境的变化,其地球化学指标具有显著的季节效应.3Ca2+、Mg2+、SO2-4能够敏感地响应极端气候事件引起的年际降水量变化,Ca2+、Mg2+、SO2-4浓度洪涝年升高,干旱年降低.HCO-3主要受CO2浓度控制,对极端气候事件响应不明显.4鸡冠洞地下河中Ca2+、Mg2+、HCO-3、SO2-4浓度波动幅度较小,且无明显的季节变化规律.对2010年和2013年的极端降水事件响应不明显.     

考虑非线性吸附时溶质在有限厚度粘土中的一维扩散解

在采用非线性分段式吸附等温模式的基础上,建立了溶质在粘土中的一维扩散模型,在考虑有限厚度边界及土中溶质背景浓度的条件下得到了相应的解.模型引入了移动边界以说明当溶质在粘土孔隙水中的浓度达到某一较高值后,阻滞因子将发生显著变化.算例分析表明,该模型和考虑经典非线性吸附等温线得到的结果相差不大,这进一步说明了该模型的合理性.考虑非线性吸附效应对溶质迁移有重要影响.在较高溶质浓度下采用线性吸附等温模式会得到偏不安全的结果.该解相对较简单,并可用于验证各种数值模型、拟合试验数据等.     

Removal of humic substances by biosorption

Fungal pellets of Aspergillus niger 405,Aspergillus ustus 326,and Stachybotrys sp.1103 were used for the removal of humic substances from aqueous solutions.Batchwise biosorption,carried out at pH 6 and 25°C,was monitored spectrophotometrically and the process described with Freundlich’s model.Calculated sorption coeffcients Kf and n showed that A.niger exhibited the highest effciency.A good match between the model and experimental data and a high correlation coeffcient(R2)pointed out to judicious choice of ...     

P-25纳米TiO2在含酚废水处理方面的应用

采用室内模拟研究,以P-25纳米TiO2作为光催化剂进行了苯酚水溶液的光催化降解性能探讨,初步考察了溶液的pH、P-25纳米TiO2用量对光催化降解苯酚过程的影响,以获得P-25纳米TiO2光降解含酚废水的较好反应条件.实验结果表明,当溶液pH=8时,降解水体中苯酚效果最佳,强酸和强碱条件均不利于苯酚的降解;在pH 8的反应体系中,当光催化剂用量为0.4g/L时,催化水体中苯酚降解的效果最好.     

多晶硅切割液废液的回收与利用

结合工程实际,介绍了太阳能产业用多晶硅片切割过程中产生的割液废液的处理工艺及回收工艺,并分析了它的投资成本和经济效益。     

杂质对硝酸铵水溶液临界爆炸温度的影响

利用自制装置对含杂质的硝酸铵水溶液临界爆炸温度进行测试研究.结果表明,Cl-单独作用在一定程度上抑制硝酸铵溶液的热分解,提高了其临界爆炸温度;pH值一定时,随着Cl-浓度的增大,硝酸铵水溶液的临界爆炸温度呈指数形式降低;Cl-浓度一定时,pH值越小,硝酸铵水溶液的临界爆炸温度越低;油脂会降低硝酸铵溶液的热稳定性.该结果...