Degradation of azo dye Acid Red 14 in aqueous solution by electrokinetic and electrooxidation process

A new wastewater treatment technology--electrokinetic-electrooxidation process (EK-EO process) is developed in this paper. The EK-EO process can take advantage of both electrooxidation on the anode surface and the electrokinetic process of anionic impurities under an electric field, which can enhance the TOC removal in electrolysis process. The degradation of an anionic azo dye Acid Red 14 (AR14) was experimentally investigated. It was found that under an electric field AR14 could be migrated into anode compartment and be efficiently mineralized. After 360 min electrolysis of 100 mgl(-1) AR14 solutions at 4.5 mAcm(-2), complete discoloration was observed in both cathode and anode compartment. About 60% TOC was electromigrated from cathode compartment to anode compartment, and more than 25 mgl(-1) TOC was abated in anode compartment. A possible degradation mechanism of AR14 by EK-EO process was proposed. Additionally, the effect of current density, recycling flux, and electrolyte concentration on the EK-EO degradation of AR14 was also investigated.     

Distribution and relationships of selected trace metals in molluscs and associated sediments from the Gulf of Aden, Yemen

Concentrations of Cd, Pb, Zn, Cu, Ni, Co, Cr, Mn and Fe in the soft tissue of Turbo coronatus, Acanthopleura haddoni, Ostrea cucullata and Pitar sp., as well as in associated surface sediments (bulk and bioavailable metal concentrations) from the Gulf of Aden, Yemen, were determined by atomic absorption spectrophotometry method. Large differences between size-classes of molluscs in metal concentrations were recorded. Significant spatial differences in metal concentrations in both the soft tissue of the molluscs and associated sediments studied were mostly identified. Statistically significant correlations (p<0.01) between concentrations of selected metals were observed. A slope of the linear regression is significantly higher than unity for Fe (9.91) and Cd (3.45) in A. haddoni and for Ni (4.15) in T. coronatus, suggesting that the bioavailability of these metals is disproportionally increased with a degree of enrichment of the sediments in Fe, Cd and Ni, respectively. A slope constant approximating to unity (1.14) for Cu in A. haddoni relative to its concentration in sediment extract implies that bioavailability of this metal proportionally increased with growing concentrations of its labile forms in the associated sediment. The degree of contamination of Gulf of Aden waters by the metals studied is discussed and the potential ability of molluscs, especially A. haddoni and T. coronatus, as biomonitors of metallic pollutants is postulated.     

催化超临界水氧化对氨基苯酚

采用CuO／γ-Al2O3和MnO2/γ-Al2O3为催化剂、H2O2为氧化剂，在一连续流固定床反应器中进行了超临界水氧化对氨基苯酚实验。实验结果表明，CuO和MnO2催化剂对于对氨基苯酚的氧化降解具有显著的促进作用。对氨基苯酚的去除率随反应温度和压力的升高、停留时间的延长而提高，在24～26MPa和400～450℃条件下，数秒钟内COD去除率可达到99％以上，催化剂CuO／γ-Al2O3的催化效果优于MnO2／γ-Al2O3。证明了催化超临界水氧化技术的高效性。     

Degradation of microcystins in aqueous solution with in situ electrogenerated active chlorine

A new and efficient method for the degradation of microcystins (one family of blue algal toxins) was developed and studied. Microcystins (MCs) in water were directly and effectively removed by active chlorine transformed in situ from the naturally existing Cl- in water resource using electrochemical method. Titanium coated with RuO2 and TiO2 was used as the anode. Microcystin-RR (MCRR) and Microcystin-LR (MCLR) were chosen as the model compounds of MCs. The results suggested that 20.87 mgl(-1) MCs (12.58 mgl(-1) MCRR and 8.29 mgl(-1) MCLR) in aqueous solution with 1.85 mM Cl- could be synchronously decomposed within 15 min electrolysis under the condition of the current density 8.89 mAcm(-2), 20 degrees C and pH 7.00. The qualitative analysis showed that the heptapetide ring and the Adda group of both treated MCs were changed. The results also indicated that the removal rates of both MCs increased with the increasing of chloride concentration and applied current density, but decreased with the increasing of initial concentration of MCs and initial pH of electrolyte. In the absence of Cl-, only a small fraction of both MCs were decomposed by direct anodic oxidation, while their almost complete removals could be obtained in the case of indirect electrooxidation with in situ electrogenerated active chlorine from Cl- in water.     

室内空气品质评价

文章介绍了室内空气品质的由来,并介绍了室内空气品质的定义,归纳了部分室内空气品质的影响因素和评价方法,提出了一些相关的改善措施.     

高速公路生活区污水处理初探

通过对高速公路生活区污水特点的分析及各种生活污水处理的工艺比较向人们提供一种适合高速公路生活区污水处理的工艺。     

两种管理科学方法在城市化SEA中的应用

城市化和城市发展已经成为世界关注的焦点。正确看待城市化SEA，并将管理科学中的方法结合，从定性到定量综合集成(meta—synthesis)引入城市化SEA进行初步探讨。     

Climatic Controls on Watershed Reference Evapotranspiration Varied during 1961–2012 in Southern China

Reference evapotranspiration (ET_o) is an important hydrometeorological term widely used in understanding and projecting the hydrological effects of future climate and land use change. We conducted a case study in the Qinhuai River Basin that is dominated by a humid subtropical climate and mixed land uses in southern China. Long‐term (1961–2012) meteorological data were used to estimate ET_o by the FAO‐56 Penman–Monteith model. The individual contribution from each meteorological variable to the trend of ET_o was quantified. We found basin‐wide annual ET_o decreased significantly (p < 0.05) by 3.82 mm/yr during 1961–1987, due to decreased wind speed, solar radiation, vapor pressure deficit (VPD), and increased relative humidity (RH). However, due to the increased VPD and decreased RH, the ET_o increased significantly (p < 0.05) in spring, autumn, and annually at a rate of 2.55, 0.56, and 3.16 mm/yr during 1988–2012, respectively. The aerodynamic term was a dominant factor controlling ET_o variation in both two periods. We concluded the key climatic controls on ET_o have shifted as a result of global climate change during 1961–2012. The atmospheric demand, instead of air temperature alone, was a major control on ET_o. Models for accurately predicting ET_o and hydrological change under a changing climate must include VPD in the study region. The shifts of climatic control on the hydrological cycles should be considered in future water resource management in humid regions.     

Kinetic and mechanism studies of the ozonolysis of three unsaturated ketones

Reaction rate constants and products of 1-octen-3-one, 3-octen-2-one and 4-hexen-3-one with ozone were studied in a 100-L fluorinated ethylene propylene (FEP) Teflon film bag using absolute rate method at 298 ± 1 K and atmospheric pressure. The rate constants were (1.09 ± 0.12) × 10^?17, (3.48 ± 0.36) × 10^?17 and (5.70 ± 0.60) × 10^?17 cm³/(molecule?sec), respectively. According to the obtained rate constants, the effects of carbonyl were discussed. The carbonyl group in β position has a net withdrawing effect with respect to an olefinic bond, then causing the decline of rate constants. The quantum chemical calculation was used to explain the results of rate constants. The products of ozonolysis were mainly aldehydes, which have significant influence on the formation of SOA, and hence play an important role in the atmosphere. In this work, we detected the main products of reaction and proposed the reaction mechanism by combining the results of quantum chemical calculations. Atmospheric lifetime for three unsaturated ketones reacted with ozone was 36.4, 11.4 and 6.9 hr for 1-octen-3-one, 3-octen-2-one and 4-hexen-3-one, respectively.