同步污水处理/发电技术-微生物燃料电池的研究进展

同步污水处理／发电技术的微生物燃料电池是利用生物催化剂直接把化学能转化为电能，具有能量转化率高、污泥产率低、反应条件温和等优点。本文阐述了微生物燃料电池的工作原理，反应器的类型及结构，综述了其最新的研究进展，并对微生物燃料电池在污水处理领域的发展方向作了展望。     

Pb、Bi连续测定综合实验设计

对Pb、Bi连续测定中的Pb、Bi废液采用Na2S沉淀,HNO3溶解后配制成分析溶液,将原来的分析实验设计成集回收和测定于一体的综合实验,使Pb、Bi溶液可以循环利用,解决了废液排放造成的Pb污染和试剂消耗,实现了化学实验的绿色化,达到了综合训练的目的。     

海明滴定法快速测定废水中的LAS含量

介绍了一种测定废水中LAS浓度的新方法。克服了常规方法亚甲基蓝比色法要绘制标准曲线，操作过程复杂等局限性。该方法测定过程简单，结果准确，标准偏差为1．4l，变异系数为3．92％。     

Long-term and seasonal nitrate trends illustrate potential prevention of large cyanobacterial biomass by sediment oxidation in Hamilton Harbour,Lake Ontario

Several studies have shown that large, experimental additions of nitrate (NO₃) to eutrophic systems can mitigate large populations of nuisance cyanobacteria and that high NO₃ concentrations can oxidize anoxic sediments. These studies are consistent with observations from numerous aquatic systems across a broad trophic range showing development of reduced surficial sediments precedes the formation of large cyanobacteria populations. We use 50+ years of data to explore whether high NO₃ concentrations may have been instrumental both in the absence of large populations of cyanobacteria in eutrophic Hamilton Harbour, Lake Ontario in the 1970s when total phosphorus (TP) and total nitrogen (TN) concentrations were high, and in delaying large populations until August and September in recent decades despite much lower TP and TN. Our results indicate that large cyanobacteria population events do not occur at the central station in July-September when epilimnetic NO₃ > 2.2 mg N L^?1. The results further suggest that remedial improvements to wastewater treatment plant oxidation capacity may have been inadvertently responsible for high NO₃ concentrations > 2.2 mg N L^?1 and thus for mitigating large cyanobacteria populations. This also implies that large cyanobacteria populations may form earlier in the summer if NO₃ concentrations are lowered.     

陶瓷原料中SiO_2的钼酸银沉淀法测定

通过实验,发现络合滴定用的指示剂——偶氮胂—Ⅲ,可用作本测定中的沉淀滴定指示剂。根据标准 AgNO_3溶液同 MoO_4~(2-)的定量反应,计算出以硅钼黄 Hg[Si(Mo_2O_7)_6]形式存在的MoO_4~(2-)量,再据以算出硅酸盐中 SiO_2的含量。     

改进的卡尔费休法滴定装置对葡萄糖酸镁水含量的测定

用带橡皮塞的导管将滴定管的上口与锥形瓶连接构成一个密闭的滴定装置，将此装置应用于卡尔费休法容量法测定水含量，在滴定过程中所有试剂与外界完全隔开，防止了空气中的水蒸气干扰，滴定终点明显。且能长时间稳定（8h以上）。该装置结构简单，操作方便。利用此方法成功测定了葡萄糖酸镁中的水含量，其平均回收率为102．0％。     

负载硫化镉的碳纳米管载镉量分析

经高温灰化法预处理后用配位滴定分析法测定负载硫化镉的碳纳米管(CdS/CNTS)的载镉量,测试数据可靠准确,表明制备负载硫化镉碳纳米管催化剂时所加入的镉并不全部吸附在碳纳米管上,载镉效率随着碳纳米管载镉量的增加而降低。     

Electrical properties of V2O5–WO3/TiO2 EUROCAT catalysts evidence for redox process in selective catalytic reduction (SCR) deNOx reaction

Electrical conductivity measurements on EUROCAT V₂O₅–WO₃/TiO₂ catalyst and on its precursor without vanadia were performed at 300°C under pure oxygen to characterize the samples, under NO and under NH₃ to determine the mode of reactivity of these reactants and under two reaction mixtures ((i) 2000 ppm NO + 2000 ppm NH₃ without O₂, and (ii) 2000 ppm NO + 2000 ppm NH₃ + 500 ppm O₂) to put in evidence redox processes in SCR deNO_x reaction.It was first demonstrated that titania support contains certain amounts of dissolved W⁶⁺ and V⁵⁺ ions, whose dissolution in the lattice of titania creates an n-type doping effect. Electrical conductivity revealed that the so-called reference pure titania monolith was highly doped by heterovalent cations whose valency was higher than +4. Subsequent chemical analyses revealed that so-called pure titania reference catalyst was actually the WO₃/TiO₂ precursor of V₂O₅–WO₃/TiO₂ EUROCAT catalyst. It contained an average amount of 0.37 at.% W⁶⁺dissolved in titania, i.e. 1.07 × 10²⁰ W⁶⁺ cations dissolved/cm³ of titania. For the fresh catalyst, the mean amounts of W⁶⁺ and V⁵⁺ ions dissolved in titania were found to be equal to 1.07 × 10²⁰ and 4.47 × 10²⁰ cm⁻³, respectively. For the used catalyst, the mean amounts of W⁶⁺ and V⁵⁺ ions dissolved were found to be equal to 1.07 × 10²⁰ and 7.42 × 10²⁰ cm⁻³, respectively. Since fresh and used catalysts have similar compositions and similar catalytic behaviours, the only manifestation of ageing was a supplementary progressive dissolution of 2.9 × 10²⁰ additional V⁵⁺ cations in titania.After a prompt removal of oxygen, it appeared that NO alone has an electron acceptor character, linked to its possible ionosorption as NO⁻ and to the filling of anionic vacancies, mostly present on vanadia. Ammonia had a strong reducing behaviour with the formation of singly ionized vacancies. A subsequent introduction of NO indicated a donor character of this molecule, in opposition to its first adsorption. This was ascribed to its reaction with previously adsorbed ammonia strongly bound to acidic sites. Under NO + NH₃ reaction mixture in the absence of oxygen, the increase of electrical conductivity was ascribed to the formation of anionic vacancies, mainly on vanadia, created by dehydroxylation and dehydration of the surface. These anionic vacancies were initially subsequently filled by the oxygen atom of NO. N^o atoms, resulting from the dissociation of NO and from ammonia dehydrogenation, recombined into dinitrogen molecules. The reaction corresponded to

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. In the presence of oxygen, NO did not exhibit anymore its electron acceptor character, since the filling of anionic vacancies was performed by oxygen from the gas phase. NO reacted directly with ammonia strongly bound on acidic sites. A tentative redox mechanism was proposed for both cases.     

Immobilization of biologically active species on PA‐6 foils treated by a dielectric barrier discharge

In the field of biomaterials and biomedical devices, surface activation has been focused on creating functional groups capable of preferential adsorption of biologically active species (proteins, enzymes, cells, drugs, etc.). In this way an interface can be created between the synthetic material and the biological medium, with the aim of increasing the compatibility of the implant with the human organism. In our experiments a dielectric barrier discharge (DBD), in helium at atmospheric pressure, was used as the source of energy capable of creating active centers that render the functionalized surface favorable to immobilization of biological molecules. Retention of immunoglobulin (IgG) and heparin biomolecules on polyamide‐6 (PA‐6) surfaces after treatment by the DBD was analyzed by atomic force microscopy, adhesion evaluation, and measurement of the contact angle titration in order to assess this incorporation on the treated surfaces. The marked adsorption of the biomolecules on the active sites created by DBD on the exposed surfaces also was related to a complex set of processes, such as enhanced roughness, increased surface wettability, and modified distribution of cationic and anionic groups on the treated surfaces. All these factors could promote interfacial interactions between the specific groups of the biomolecules existing in the biological medium and the type of cationic and/or anionic groups present on the surface. The efficiency of the DBD treatment showed that the DBD technique is useful for preactivation of the polymer surface for immobilization of other biologically active species (such as drugs and enzymes). © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1985–1990, 2003     

甲氧胺盐酸盐的含量测定方法

提出了以酚酞为指示剂，氢氧化钠为滴定剂测定甲氧胺盐酸盐含量的方法。测定了甲氧胺盐酸盐的离解常数Ka，考察了干扰因素对测定的影响。结果表明，干扰物质NH4Cl在样品中的含量小于5％不影响测定。该方法具有简便、快速，准确等特点,测定了数批样品结果较满意。