海洋耐镉微生物筛选及其生物学特性

从重金属污染的近海域筛选到一株对镉具有较强抗性和富集能力的微生物Cd20002,该菌株在液体培养基中的最大耐受浓度为1 000 mg/L,在镉浓度达到200 mg/L时,其吸附率高达93.4%,根据形态特征和生理生化鉴定及16S rRNA测序鉴定为蓝杆菌。通过在不同的镉浓度环境对蓝杆菌Cd20002进行培养,测定其生长曲线,并优化菌体生长的条件及其吸附能力。结果表明,蓝杆菌Cd20002既能在重金属镉环境中生存,且富镉能力较强,对水产环境中重金属的生物清排具有重要意义。     

Ce-promoted Mn/ZSM-5 catalysts for highly efficient decomposition of ozone

Manganese oxides supported by ZSM-5 zeolite (Mn/ZSM-5) as well as their further modified by Ce promoter were achieved by simple impregnation method for ozone catalytic decomposition. The yCe20Mn/ZSM-5–81 catalyst with 8% Ce loading showed the highest catalytic activity at relative humidity of 50% and a space velocity of 360 L/(g × hr), giving 93% conversion of 600 ppm O₃ after 5 hr. Moreover, this sample still maintained highly activity and stability in humid air with 50%–70% relative humidity. Series of physicochemical characterization including X-ray diffraction, temperature-programmed technology (NH₃-TPD and H₂-TPR), X-ray photoelectron spectroscopy and oxygen isotopic exchange were introduced to disclose the structure-performance relationship. The results indicated that moderate Si/Al ratio (81) of zeolite support was beneficial for ozone decomposition owing to the synergies of acidity and hydrophobicity. Furthermore, compared with 20Mn/ZSM-5-81, Ce doping could enhance the amount of low valance manganese (such as Mn²⁺ and Mn³⁺). Besides, the Ce³⁺/Ce⁴⁺ ratio of 8Ce20Mn/ZSM-5-81 sample was higher than that of 4Ce20Mn/ZSM-5-81. Additionally, the synergy between the MnO_x and CeO₂ could easily transfer electron via the redox cycle, thus resulting in an increased reducibility at low temperatures and high concentration of surface oxygen. This study provides important insights to the utilization of porous zeolite with high surface area to disperse active component of manganese for ozone decomposition.     

Oxidation of diesel soot on binary oxide CuCr(Co)-based monoliths

Binary oxide systems(Cu Cr2O4, Cu Co2O4), deposited onto cordierite monoliths of honeycomb structure with a second support(finely dispersed Al2O3), were prepared as filters for catalytic combustion of diesel soot using internal combustion engine’s gas exhausts(O2, NOx, H2 O, CO2) and O3 as oxidizing agents. It is shown that the second support increases soot capacity of aforementioned filters, and causes dispersion of the particles of spinel phases as active components enhancing thereby catalyst activity and selectivity of soot combustion to CO2. Oxidants used can be arranged with reference to decreasing their activity in a following series: O3 NO2> H2 O > NO > O2> CO2. Ozone proved to be the most efficient oxidizing agent: the diesel soot combustion by O3 occurs intensively(in the presence of copper chromite based catalyst) even at closing to ambient temperatures.Results obtained give a basis for the conclusion that using a catalytic coating on soot filters in the form of aforementioned binary oxide systems and ozone as the initiator of the oxidation processes is a promising approach in solving the problem of comprehensive purification of automotive exhaust gases at relatively low temperatures, known as the "cold start" problem.     

Comparisons of the film peeling from the composite oxides of quartz sand filters using ozone, hydrogen peroxide and chlorine dioxide

To solve the problem of shortened backwashing intervals in groundwater plants, several disinfectants including ozone (O₃), hydrogen peroxide (H₂O₂) and chlorine dioxide (ClO₂) were examined to peel off the film from the quartz sand surface in four pilot-scale columns. An optimized oxidant dosage and oxidation time were determined by batch tests. Subsequently, the optimized conditions were tested in the four pilot-scale columns. The results demonstrated that the backwashing intervals increased from 35.17 to 54.33 (H₂O₂) and to 53.67 hr (ClO₂) after the oxidation treatments, and the increase of backwashing interval after treatment by O₃ was much less than for the other two treatments. Interestingly, the treatment efficiency of filters was not affected by O₃ or H₂O₂ oxidation; but after oxidation by ClO₂, the treatment efficiency was deteriorated, especially the ammonia removal (from 96.96% to 24.95%). The filter sands before and after the oxidation were characterized by scanning electron microscopy and X-ray photoelectron spectroscopy. Compared with the oxidation by O₃ and H₂O₂, the structures on the surface of filter sands were seriously damaged after oxidation by ClO₂. The chemical states of manganese on the surfaces of those treated sands were only changed by ClO₂. The damage of the structures and the change of the chemical states of manganese might have a negative effect on the ammonia removal. In summary, H₂O₂ is a suitable agent for film peeling.     

嗜盐菌相溶物质合成与转运调节机制

嗜盐菌是极端环境微生物的重要类群之一,作为新型微生物资源,为微生物生理、遗传分类及生命科学和相关学科许多领域的研究提供新的课题.文章综述了嗜盐菌的嗜盐渗透压分子调节机理中,相溶物质胞外吸收转运与胞内生物合成途径涉及的结构基因、主要酶类的相关研究进展,并对后续研究进行讨论与展望.     

Screening the emission sources of volatile organic compounds (VOCs) in China by multi-effects evaluation

We develop a multi-effect evaluation method to assess integrated impact of VOCs. Enable policy-makers to identify important emission sources, regions, and key species. Solvent usage and industrial process are the most important anthropogenic sources. Styrene, toluene, ethylene, benzene, and m/p-xylene are key species to be cut. Volatile organic compounds (VOCs) play important roles in the atmosphere via three main pathways: photochemical ozone formation, secondary organic aerosol production, and direct toxicity to humans. Few studies have integrated these effects to prioritize control measures for VOCs sources. In this study, we developed a multi-effects evaluation methodology based on updated emission inventories and source profiles, by combining the ozone formation potential (OFP), secondary organic aerosol potential (SOAP), and VOC toxicity data. We derived species-specific emission inventories for 152 sources. The OFPs, SOAPs, and toxicity of each source were estimated, the contribution and sharing of source to each of these adverse effects were calculated. Weightings were given to the three adverse effects by expert scoring, and then the integrated effect was determined. Taking 2012 as the base year, solvent use and industrial process were found to be the most important anthropogenic sources, accounting for 24.2% and 23.1% of the integrated effect, respectively, followed by biomass burning, transportation, and fossil fuel combustion, each had a similar contribution ranging from 16.7% to 18.6%. The top five industrial sources, including plastic products, rubber products, chemical fiber products, the chemical industry, and oil refining, accounted for nearly 70.0% of industrial emissions. Beijing, Chongqing, Shanghai, Jiangsu, and Guangdong were the five provinces contributing the largest integrated effects. For the VOC species from emissions showed the largest contributions were styrene, toluene, ethylene, benzene, and m/p-xylene.     

Air quality improvement in Los Angeles—perspectives for developing cities

Air quality improvement in Los Angeles can inform air quality policies in developing cities. Emission control efforts, their results, costs and health benefits are briefly summarized. Today's developing cities face new challenges including regional pollution. Air quality issues in Beijing are briefly compared and contrasted with Los Angeles. Opportunities for co-benefits for climate and air quality improvement are identified. Air quality improvement in Los Angeles, California is reviewed with an emphasis on aspects that may inform air quality policy formulation in developing cities. In the mid-twentieth century the air quality in Los Angeles was degraded to an extent comparable to the worst found in developing cities today; ozone exceeded 600 ppb and annual average particulate matter <10 mm reached ~150 mg·m⁻³. Today's air quality is much better due to very effective emission controls; e.g., modern automobiles emit about 1% of the hydrocarbons and carbon monoxide emitted by vehicles of 50 years ago. An overview is given of the emission control efforts in Los Angeles and their impact on ambient concentrations of primary and secondary pollutants; the costs and health benefits of these controls are briefly summarized. Today's developing cities have new challenges that are discussed: the effects of regional pollution transport are much greater in countries with very high population densities; often very large current populations must be supplied with goods and services even while economic development and air quality concerns are addressed; and many of currently developing cities are located in or close to the tropics where photochemical processing of pollution is expected to be more rapid than at higher latitudes. The air quality issues of Beijing are briefly compared and contrasted with those of Los Angeles, and the opportunities for co-benefits for climate and air quality improvement are pointed out.     

Application of a long-path differential optical absorption spectrometer (LP-DOAS) on the measurements of NO(2), SO(2), O(3), and HNO(2) in Gwangju, Korea

A differential optical absorption spectrometer (DOAS) technique has been applied to monitor airborne trace pollutants including NO(2), SO(2), O(3), and HNO(2) in the ultraviolet (UV) region (290-350 nm) over a 1.5 km beam path (two ways) during an intensive measurement campaign held at Gwangju, Korea (March 2002). Their mean mixing ratios (and standard deviations) were computed as 11.3 (8.8), 1.9 (1.7), 17.1 (19.3), and 0.5 (0.4)ppbv, respectively. As a means to evaluate the performance of the long-path DOAS (LP-DOAS) system with conventional point monitoring systems (PMS), correlation analysis was conducted between the two data sets. These data sets were then inspected to account for the influence of the environmental conditions on the correlation strength between the two systems, especially with respect to light level and wind speed. To facilitate the comparison, correlation analyses were conducted after dividing the data sets for those parameters into several classes. The strength of the correlations between DOAS and meteorological parameters was also examined to evaluate their effects on the DOAS performance. It was found that, among the four pollutant species, O(3) is the most sensitive to changes in meteorological conditions in relation with atmospheric mixing conditions. The overall results of our study indicate that open-path monitoring techniques can be used to effectively diagnose air quality and be substituted for the conventional point monitoring methods with the proper consideration of those parameters affecting the DOAS sensitivity (e.g., light level and wind speed).     

Ozone risk assessment for plants: central role of metabolism-dependent changes in reducing power

The combination of stomatal-dependent ozone flux and total ascorbate level is currently presented as a correct indicator for determining the degree of sensitivity of plants to ozone. However, the large changes in carbon metabolism could play a central role in the strategy of the foliar cells in response to chronic ozone exposure, participating in the supply of reducing power and carbon skeletons for repair and detoxification, and modifying the stomatal mode of functioning. To reinforce the accuracy of the definition of the threshold for ozone risk assessment, it is proposed to also consider the redox pool (NAD(P)H), the ratio between carboxylases and the water use efficiency as indicators of the differential ozone tolerance of plants.     

Decomposing detonation and deflagration properties of ozone/oxygen mixtures

In this study, the decomposing detonation and deflagration properties of ozone/oxygen mixtures of up to 20 vol.% of ozone in oxygen under high pressure of up to 1.0 MPa in a tube were experimentally investigated. The mixtures were ignited by an electric spark at the end of the tube. Flame propagation properties such as flame velocity and pressure were measured with thermocouples and piezo electric transducers mounted along the tube. Slow and constant flame propagation profiles were obtained. We also investigated the quenching ability of a wire gauze as well as the concentration limit for flame propagation. However, in spite of slow flame propagation velocity and easy flame quenching properties under these experimental conditions, direct initiation of detonation by the driver detonation of the stoichiometric oxy-hydrogen mixture was easily achieved at much lower concentrations than the limit of deflagration. The observed detonation properties, such as wave velocity and pressure, agreed fairly well with C–J calculated values. The detonation velocity (900–1200 m/s) and the pressure ratio to initial pressures (5–9.5) were not affected by the initial pressure of the mixtures. Near the detonation limit, typical spinning detonations with oscillatory pressure waves were observed.