水体氧化性氯的环境行为与生态风险研究进展

氧化性氯是一类常用的含氯氧化剂,在市政水处理、工业水系统、卫生环保等领域常用作消毒药剂。为保证消毒效果,其使用量通常做过量处理。剩余氧化性氯可能进入水体环境并对水生生物产生潜在危害效应,影响水生生态系统平衡。本文主要总结氧化性氯在水环境中的来源与分布、水环境行为及其水生态风险,并就水体氧化性氯对水生环境的影响研究进行展望。

氯类氧化性杀菌剂效果增强的研究

在循环冷却水系统中氯类氧化性杀菌剂存在持效时间短、剥离性能差的缺点。作者介绍了氯类氧化性杀菌剂配合WL-12活性增效分散剂的使用情况,对其杀菌效果和持效时间进行了评价。并通过现场应用,评价了两种药剂配合使用后的剥离性能。

反渗透复合膜最新研究进展

反渗透膜在海水淡化、超纯水制备、污水处理、制药及生物技术等领域得到了广泛应用.目前,最成功的反渗透膜是通过界面聚合方法制备的以交联聚酰胺为分离皮层的复合膜.交联聚酰胺皮层的结构和性质对最终反渗透膜的分离性能起关键作用.本文简要介绍了界面聚合复合膜的形成过程和结构、新型界面聚合功能单体、界面聚合反应添加剂、纳米杂化反渗透复合膜、高耐氯氧化性反渗透膜,以及反渗透复合膜表征方法创新等方面的研究进展和发展趋势.

Direct Synthesis of Phenol from Benzene on an Activated Carbon Catalyst Treated with Nitric Acid

Commercially available coal-based activated carbon was treated by nitric acid with different concentrations and the resultant samples were used as catalysts for the direct hydroxylation of benzene to phenol in acetonitrile. Boehm titration, X-ray photoelectron spectroscopy, scanning electron microscope coupled with an energy dispersive X-ray microanalyzer, and Brunauer-Emmett-Teller method were used to characterize the samples. The number of carboxyl groups on the surface was found to be the main factor affecting the catalytic activity. An optimum catalytic performance with a yield of 15.7% and a selectivity of 87.2% to phenol was obtained.

Effect of Sodium Chloride and Cadmium on the Growth, Oxidative Stress and Antioxidant Enzyme Activities of Zygosaccharomyces rouxii

Zygosaccharomyces rouxii is a salt-tolerant yeast species capable of removing cadmium(Cd) pollutant from aqueous solution. Presently, the physiological characteristics of Z. rouxii under the stress of sodium chloride(NaCl) and Cd are poorly understood. This study investigated the effects of NaCl and Cd on the growth, oxidative stress and antioxidant enzyme activities of Z. rouxii after stress treatment for 24 h. Results showed that NaCl or Cd alone negatively affected the growth of Z. rouxii, but the growth-inhibiting effect of Cd on Z. rouxii was reduced in the presence of NaCl. Flow cytometry assay showed that under Cd stress, NaCl significantly reduced the production of reactive oxygen species(ROS) and cell death of Z. rouxii compared with those in the absence of NaCl. The activities of superoxide dismutase(SOD), catalase(CAT), and peroxidase(POD) of Z. rouxii were significantly enhanced by 2%–6% NaCl, which likely contributed to the high salt tolerance of Z. rouxii. The POD activity was inhibited by 20 mg L-1Cd while the SOD and CAT activities were enhanced by 8 mg L-1 Cd and inhibited by 20 mg L-1 or 50 mg L-1 Cd. The inhibitory effect of high-level Cd on the antioxidant enzyme activities of Z. rouxii was counteracted by the combined use of NaCl, especially at 6%. This probably accounted for the decrease in Cd-induced ROS production and cell death of Z. rouxii after incubation with NaCl and Cd. Our work provided physiological clues as to the use of Z. rouxii as a biosorbent for Cd removal from seawater and liquid highly salty food.

Electrooxidative Degradation of an Anthraquinone Dye with in-situ Electrogenerated Active Chlorine in a Divided Flow Cell

The purpose of this paper was to investigate the possibility of treating C. I. Reactive Blue 19 wastewater by electrochemical oxidation via electrogenerated active chlorine, using metallic oxide coatings （dimensional stable anode, DSA） as anode. The electrolysis for the simulated wastewater was conducted at a constant current. Absorbances at 592 nm and 255 nm were measured to follow the decolorization of the dye and the degradatin of its aromatic ring. After 4 h of electrolysis under the experimental conditions： current density of 15 A·m^-2, 0.2 mol·L^-1 NaCl, 0.1 mol·L^-1 Na2SO4, 0.1 mmol·L^-1 dye, initial pH=6.4 and T=30℃, 100% decolorization of the dye and about 45% degradation of its aromatic ring were achieved, while no obvious change of total organic carbon was observed. The experimental results suggest that the decolorization of the dye and degradation of its aromatic ring were directly affected by current density, temperature, concentrations of the dye and sodium chloride, while slightly affected by initial pH and sodium sulfate concentration; the decolorization of the dye and degradation of its aromatic ring followed pseudo-first-order kinetics; and indirect electrooxidation, using electrogenerated active chlorine, predominated in the electrochemical oxidation.

Negundoside,an irridiod glycoside from leaves of Vitex negundo,protects human liver cells against calcium-mediated toxicity induced by carbon tetrachloride

AIM： To evaluate the protective effect of 2′-p-hydroxy benzoylmussaenosidic acid [negundoside （NG）, against carbon tetrachloride （CCl4）-induced toxicity in HUH-7 cel Is.METHODS： CCI4 is a well characterized hepatotoxin, and inducer of cytochrome P450 2E1 （CYP2E1）-mediated oxidative stress. In addition, lipid peroxidation and accumulation of intracellular calcium are important steps in the pathway involved in CCl4 toxicity. Liver cells （HUH-7） were treated with CCI4, and the mechanism of the cytoprotective effect of NG was assessed. Silymarin, a known hepatoprotective drug, was used as control. RESULTS： NG protected HUH-7 cells against CCl4 toxicity and loss of viability without modulating CYP2E1 activity. Prevention of CCl4 toxicity was associated with a reduction in oxidative damage as reflected by decreased generation of reactive oxygen species （ROS）, a decrease in lipid peroxidation and accumulation of intracellular Ca^2＋ levels and maintenance of intracellular glutathione homeostasis. Decreased mitochondrial membrane potential （MMP）, induction of caspases mediated DNA fragmentation and cell cycle arrest, as a result of CCl4 treatment, were also blocked by NG. The protection afforded by NG seemed to be mediated by activation of cyclic adenosine monophosphate （cAMP） synthesis and inhibition of phospholipases （cPLA2）. CONCLUSION： NG exerts a protective effect on CYP2E1-dependent CCl4 toxicity via inhibition of lipid peroxidation, followed by an improved intracellular calcium homeostasis and inhibition of Ca^2＋-dependent proteases.

Ordinary Toxicity of Chlorine Dioxide and By-products Chlorite and Chlorate in Water

Acute toxicity and accumulated toxicity of chlorine dioxide (ClO2) and by-products chlorite (ClO2-) and chlorate (ClO3-) in water acted on mice are studied by the method of Horn and accumulation coefficient. Subchronic toxicity of the mixture of ClO2 and ClO2-and ClO3- in water acted on rat is studied though feeding test for 90 days, including statistical analysis of variance on weight gaining, food utilization efficiency,index of blood and serum,liver (or kidney) to body weight ratio, and histopathological examination on liver and kidney. The results show that aqueous solution of ClO2, NaClO2 and NaClO3 ( with the concentration of 276.5 mg/L, 200 mg/L and 200 mg/L respectively) and the mixed aqueous solution of ClO2 with the concentration of 553 mg/L are actually non-poisonous , and non-cumulative aqueous solution as well.

Valence variation of arsenic in bioleaching process of arsenic-bearing gold ore

The concentration and variational trend of As3 +and As 5+,the bacterial resistance for the As 3+and As 5+and converting conditions from As3 +to As 5+were analyzed.The additive was used to prompt the bacterial leaching efficiency by changing valence state of arsenic.The results show that the concentration of As 3+ is larger than that of As 5+ in the lag phase.The concentration of As 3+ decreases in the log phase,and is lower than that of As5 +.HQ-0211 typed bacteria express better resistance for As 3+and As 5+and remain growing when the concentrations of As3 +and As 5+are above 6.0 g/L and 12.0 g/L,respectively.It is found that Fe 3+cannot oxidize As3 +singly as strong oxidant in the leaching system,but can cooperate with pyrite or chalcopyrite to do that.The oxidation of As 3+ is prompted with addition of H2O2.The bacterial activity is improved in favor of bacterial leaching efficiency.NaClO restrains the bacterial growth to depress leaching efficiency because of the chloric compounds affecting bacterial activity.

Effects of Mercuric Chloride on Antioxidant System and DNA Integrity of the Crab Charybdis japonica

Mercury （Hg） is one of the commonly encountered heavy metals, which is widespread in inshore sediments of China. In order to investigate the toxicity of Hg on marine invertebrates, we studied the effects of the divalent mercuricion （Hg2＋） （at two final concentrations of 0.0025 and 0.0050mgL-1, prepared with HgC12） on metallothionein （MT） content, DNA integrity （DNA strand breaks） and catalase （CAT） in the gills and hepatopancreas, antioxidant enzyme activities of superoxide dismutase （SOD）, catalase （CAT） and glutathione peroxidase （GPx）, in the hemolymph, gills and hepatopancreas of the portunid crab Chao,bdisjaponica for an experiment period up to 15 d. The results indicated that MT was significantly induced after 3 d, with a positive correlation with Hg2＋ dose and time in the hepatopancreas and a negative correlation with Hg2＋ dose and time in the gills. While CAT in the hemolymph was not detected, it increased in the hepatopancreas during the entire experiment; SOD and GPx in the three tissues were stimulated after 12h, both attained peak value and then reduced during the experimental period. Meanwhile, DNA strand breaks were all induced significantly after 12 h. These results suggested the detoxification strategies against Hg2＋ in three tissues of C. japonica.

Oxygen and nitrogen-doped metal-free carbon catalysts for hydrochlorination of acetylene

Activated carbon was tested as metal-free catalyst for hydrochlorination of acetylene in order to circumvent the problem of environment pollution caused by mercury and high cost by noble metals. Oxygen-doped and nitrogen-doped activated carbons were prepared and characterized by XPS, TPD and N2 physisorption methods. The influences of the surface functional groups on the catalytic performance were discussed base on these results. Among all the samples tested, a nitrogen-doped sample, AC-n-US00, exhibited the best performance, the acety- lene conversion being 92% and vinyl chloride selectivity above 99% at 240 ~C and C2H2 hourly space velocity 30 h- 1. Moreover, the AC-n-US00 catalyst exhibited a stable performance during a 200 h test with a conversion of acetylene higher than 76% at 210 ~C at a C2H2 hourly space velocity 50 h 1. In contrary, oxygen-doped catalyst had lower catalytic activities. A linear relationship between the amount of pyrrolic-N and quaternary-N species and the catalytic activity was observed, indicating that these nitrogen-doped species might be the active sites and the key in tuning the catalytic performance. It is also found that the introduction of nitrogen species into the sample could significantly increase the adsorption amount of acetylene. The deactivation of nitrogen- doped activated carbon might be caused by the decrease of the accessibility to or the total amount of active sites.

New insights into enhancement of sodium hypochlorite on formation and properties of anodic films on Ti6Al4V alloy

Anodic films were successfully fabricated on Ti6A14V alloy by anodic oxidation method in an environmental friendly electrolyte with and without sodium hypochlorite. The anodic films were characterized by means of the scanning electron microscope （SEM） and energy dispersive spectrometer （EDS）. Results revealed that the addition of sodium hypochlorite leads to the ultrafast growth of oxide films, and results in the significant changes of morphology and thickness. The influence of sodium hypochlorite on formation and crystallization of oxide films as a function of anodizing time was discussed. Meanwhile, potentiodynamic electrochemical tests and dry sliding wear tests were performed to evaluate the corrosion resistance and tribological properties of oxide films. It was found that the oxide film fabricated with the existence of sodium hypochlorite had improved corrosion resistance and tribological properties than the one formed without sodium hypochlorite. Moreover, the effect mechanism of sodium hypochlorite on the growth rate and surface morphologies of oxide films during the anodizing process was discussed. It was found that hypochlorite ions participated in the reaction on anode which causes the rapid growth of oxide films and then affect the whole anodizing process.

The Porous Ramie Fabric＇s Heat-Moisture Comfort

This paper in the light of the structure parameters of the ramie fabric to research and evaluation it＇s heart-moisture comfort. Selected 15 kinds of ramie fabric to test the average density, the thickness, the tightness, the heat rate, the heat transfer coefficient, the Clo, the air permeability, the water vapor permeability and other performance index, used SPSS factor analysis to explore the main influence factors of porous ramie fabric＇s heat moisture comfort. Results shows that： the main influence factors of ramie fabric＇s heat-moisture is the heat preservation material, the air permeability and the moisture permeability, get the equation of porous ramie fabric＇ s heat-moisture comfort： F=0.45855y1＋0.30588y2＋0.13549y3, evaluated and sorted the sample fabric＇ s heat-moisture comfort.

Modification of methyl oleate for silicon-based biological lubricating base oil

A new kind of silicon-based biological lubricating base oil with good viscosity-temperature behavior,viscosity index,thermostability,oxidation stability and wear resistance performance was synthesized as a derivative of methyl oleate.Trimethylsilylation reaction was introduced to further improve methyl oleate oxidation stability and lubricity after epoxidation and open-ring reactions.The order of effectiveness of acid binding agent was N,N-diisopropylethylamine(DIEA) > pyridine > diethylamine > triethylamine,and the effects of various parameters on the trimethylsilylation reaction as well as on the silicon-oxygen bond stability and reaction yield were studied.A maximum yield of 34.54%was achieved at hydroxyl/trimethyl chlorosilane/DIEA molar ratio of1:1.25:1,reaction temperature 40℃,reaction time 1.5 h.

Ceria in halogen chemistry

Halogen chemistry constitutes an essential part in the industrial production of polymers and gains increasing attention as an attractive strategy to activate light alkanes that constitute natural gas. CeO2-based catalysts offer an exciting potential for advances in hydrogen halide recovery that enables a high efficiency of halogen-based processes for activation of small molecules. This review provides an overview of recently developed ceria-based catalysts in the context of polymer industry(polyvinyl chloride, polyurethanes, and polycarbonates) and activation of light hydrocarbons for natural gas upgrading. In addition, mechanistic insight and the challenges of ceria catalysts are provided, aiding the design of future catalytic materials and applications.

The Role of the Dipole Interaction of Molecules with Charged Particles in the Polar Stratosphere

Our analysis of published results of experiments in the Polar Regions substantiates and further develops our new approach to the photochemical processes in the polar stratosphere involving the charged particles. The dipole interaction of molecules with charged particles, primarily with ions, leads to the adhesion and disintegration of a number of molecules including ozone. Molecules acquire additional energy on the surface of the charged particles, enabling reactions that are not possible in space. Galactic cosmic rays are the main source of ions in the polar stratosphere, their equilibrium concentration at altitudes of 15 to 25 km can reach up ~ （1-5） ~ 103 ions/cm3. Estimations show that if the ozone destruction in the regime of＂collision＂ with ions then the lifetime of ozone will vary from 10 days to 2 months. We suppose that alongside with the chlorine mechanism of ozone destruction there is a mechanism of ozone decay on a charged particle which can act also at those latitudes and altitudes where chlorine oxide CIO is absent, as well as in the night conditions. Here, we demonstrated the close connection of photochemical processes with the dynamic, electrical and condensational phenomena in the stratosphere, in particular, with the accumulation of unipolar charged particles on the upper and lower boundaries of the polar stratospheric clouds and aerosol layers as a result of the activity of the global electric circuit.

Hemin-histamine-montmorillonite clay conjugate as a model biocatalyst to mimic natural peroxidase

We successfully synthesized the first hemin-montmorillonite bio-conjugate with an amino acid residue to mimic natural peroxidase enzyme. Histamine was intercalated in montmorillonite by cation exchange, then a heroin molecule was loaded onto the histamine-montmorillonite with an adsorption capacity of 7.0 mg· g^-1. The hemin-histamine-montmorillonite conjugate shows high peroxidase activity as indicated by the oxidation of guaiacol, which is attributed to the activation of hemin by Fe-N complex formation between the imidazole group in histamine and the iron ion in the hemin molecule. Temperaturedependent peroxidase activity for this synthesized biomimetic material indicates that raising the reaction temperature could significantly enhance the activity of the conjugate. The biomimetic catalyst has good reusability; nearly 100% activity can be retained after three cycles. Because montmorillonite clay is widely distributed in the environment, this material offers great potential for in situ and ex situ remediation of many organic contaminants in surface/subsurface soils.

Influence of Cl substitution on the electronic structure and catalytic activity of ceria

Cl-containing cerium dioxide(Ce O2) catalysts have been found to exhibit unique catalytic activities. In the present work, using density functional theory calculations with the inclusion of on-site Coulomb correction, we systematically studied the effect of Cl on the physicochemical properties of Ce O2 surfaces by substituting one subsurface O with Cl. The calculated results show that substituting an O atom with a Cl atom results in structural distortion and the reduction of one surface Ce4+ cation to Ce3+. The protruding Ce3+ cation greatly improves the adsorption energy of O2 to produce an active O2- species, and maintains the catalytic oxidation cycle of CO on Ce O2(110). These results may help us obtain a better understanding of Cl-ceria interacting systems and provide some guidance for the design of effective Ce O2-based catalysts.