Photochemical reaction of particle-bound 1-nitropyrene under simulated atmospheric condition

Photoreaction of particle-bound 1-nitropyrehe (1-NP) under simulated atmospheric condition has been studied. When 1-NP coated on the surface of silica gel was suspended in a stream of nitrogen, oxygen or air, respectively, and exposed to intensive light of xenon lamp, photochemical reaction took place. The result of kinetic study showed it to be of the second order. The photoreaction products were identified by off-line HPLC/MS as 1,6-pyrenequinone, 1,8-pyrenequinone, trinitro-hydroxypyrene, dinitrohydroxypyrene, 6,6'- dipyrenenone, etc. The mutagenicity of photochemical reaction products is higher in oxygen and air, and lower in nitrogen than that of the precursor 1-NP, as detected by the Ames Bioassay.     

对总磷测定中样品消解加热时间的探讨

三组对照实验表明，地面水总磷的测定和消解时间可由30min缩减到15min.     

Quantification of the effects of management factors on maize (Zea mays L.) and cotton (Gossypium hirsutum L.) residues decomposition rate

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Thermal behaviors, combustion mechanisms, evolved gasses, and ash analysis of spent potlining for a hazardous waste management

An unavoidable but reusable waste so as to enhance a more circular waste utilization has been spent potlining (SPL) generated by the aluminum industry. The combustion mechanisms, evolved gasses, and ash properties of SPL were characterized dynamically in response to the elevated temperature and heating rates. Differential scanning calorimetric (DSC) results indicated an exothermic reaction behavior probably able to meet the energy needs of various industrial applications. The reaction mechanisms for the SPL combustion were best described using the 1.5-, 3- and 2.5-order reaction models. Fluoride volatilization rate of the flue gas was estimated at 2.24%. The SPL combustion emitted CO₂, HNCO, NO, and NO₂ but SO_x. The joint optimization of remaining mass, derivative thermogravimetry, and derivative DSC was achieved with the optimal temperature and heating rate combination of 783.5°C, and 5 °C/min, respectively. Interaction between temperature and heating rate exerted the strongest and weakest impact on DSC and remaining mass, respectively. The fluorine mainly as the formation of substantial NaF and CaF₂ in the residual ash. Besides, the composition and effect of environment of residual solid were evaluated. The ash slagging tendency and its mineral deposition mechanisms were elucidated in terms of turning SPL waste into a benign input to a circular waste utilization.     

Carboxylic acids in the troposphere, occurrence, sources, and sinks: A review

Carboxylic acids are ubiquitous and important components of the troposphere; they are currently measured in different environments. They are thought to have several sources comprising primary biogenic and anthropogenic emissions, hydrocarbons gas-phase oxidations, and some carbonyl compounds aqueous-phase oxidations. In the present review we make a synthesis of the concentrations of low molecular weight carboxylic acids in tropospheric aqueous and gaseous phases and in aerosol particles for different environments. We also successively examine the major sources of carboxylic acids and discuss their relative contribution to tropospheric concentrations for various environments as well as the principal sinks of these compounds.     

非平衡等离子体技术对有害气体污染物的降解研究进展

由于非平衡等离子体化学过程在增强氧化能力、促进分子离解以及加速化学反应等方面具有很高的效率 ,因此 ,近年来利用非平衡等离子技术对气体污染物的破坏分解研究受到了广泛的关注。本文简述了非平衡等离子体技术对气体污染物的降解原理 ,综述了国内外利用这一技术破坏各种气体污染物的最新进展 ,讨论了放电功率、停留时间、催化剂、化合物结构等因素对放电反应效率的影响 ,并展望了其应用前景     

秆粪肥在赤红壤中的矿化研究

采用十一种有机物肥进行矿化研究，肥效试验设高、中、低化肥水平比较．结果表明：（１）不同肥料对玉米苗期干物重的影响是：粪肥＞化肥＞秆肥．施入６２ｄ，土场总碳量是，施粪肥的比对照高１．３７倍，施秆肥的高１．２４倍，单施化肥的反比对照下降１４．３％。当然，不同秆粪肥的肥效也不完全一样．（２）在南方高温多雨的条件下，秆粪肥施入土壤后的分解是很快的，尤其是施后的第一个月，其分解速率杠肥平均为４３．４％；粪肥为３５．４％．秆肥中分解最快的是玉米秆，最慢的是甘蔗渣，分解速率分别为５０．１％和２３．４％；粪肥中分解最快的是鸡粪，最慢的是鸭粪，分解速率分别为５５．７％和２１．５％．一个月后分解速率则明显下降．秆粪肥在土壤中的分解一直延缓到三年以后。（３）施后第一年的腐殖化系数，秆肥为２．５４３×１０（－３）－４．３１９×１０（－３），其中番薯藤的最大，黄豆秆的最小；粪肥的除鸡粪和猪粪较小外，牛、鸭粪的达４×１０（－３）以上。一年以后便逐年明显减小．     

北京地区对流层低层臭氧及硫酸盐气溶胶的时空分布

基于OMI/Aura卫星资料,分析了北京地区2007~2016年近10a对流层O₃浓度（0~3km）、硫酸盐气溶胶光学厚度（0~2km）、SO₂（边界层以内）柱浓度时空演变特征.结果表明,近10a来北京地区O₃浓度总体呈现上升趋势,最低值在2007年,浓度为33.65 μg/m³;硫酸盐气溶胶污染总体变化呈现先下降后增长的趋势,2007年硫酸盐气溶胶污染最为严重,2011年污染最轻,对应的AOD值为0.252,但在2014年以后,硫酸盐气溶胶污染又出现增长趋势;SO₂浓度在2007~2016年总体呈现下降的变化趋势,且下降趋势明显,最高值为2007年,最低值出现在2016年,最低值比最高值降低了60.42%,但在2011年污染出现反弹.北京O₃季节变化明显,夏季高、春秋次之、冬季低;硫酸盐气溶胶污染季节特征与O₃相同;SO₂污染主要集中在冬季,采暖期污染程度高于非采暖期.     

VOCs released from municipal solid waste at the initial decomposition stage: Emission characteristics and an odor impact assessment

The nuisance from odor caused by municipal solid waste (MSW) is resulting in a growing number of public complaints and concerns. Odor pollution occurs in the initial decomposition stage of MSW, including waste collection, transportation and early pre-treatment. Furthermore, decomposition takes place in waste facilities that are often close to living areas, which can result in odor impacts on local inhabitants. However, this aspect of odor impact from MSW has not been well studied. In the current study, lab-scale waste cells were designed to simulate MSW storage conditions in the early stage. The characteristics of VOCs emissions with different waste compositions were analyzed. The odor concentration (C_O, non-dimensional) method and odor intensity were used for the assessment of odor. Ethanol was the substance with highest emission rate. The release rate of VOCs increased with the growth easily biodegradable waste (EBW). VOCs emissions was reduced by 25% when the proportion of EBW decreased from 60% to 45%. Methyl sulfide, ethanol, dimethyl disulfide and ethyl acetate were identified as typical odorants. The EBW proportion in waste is the main factor significantly influencing odor pollution. The C_O was 244.51 for the 60% EBW condition, which was only 61.46 for 15% EBW condition. These study results provide important information for the implementation of a garbage sorting policy and the monitoring of odor pollution from waste management.     

基于结构分解法的长江经济带产业排水量驱动因素评估

为分析长江经济带产业排水量变化的驱动因素,以2002年、2007年和2012年长江经济带11省市投入产出表、排水估计量为基础,利用基于投入产出的结构分解法对各省市数据进行比较静态分析,对驱动产业排水量变化的因素进行分解及定量评估,包括节水减排效应、投入结构效应、需求结构效应及规模效应.结果表明:①长江经济带产业排水量由增长趋势变为下降趋势,2002—2007年排水量增长了16.9%,2007—2012年排水量降低了0.4%,2002年、2007年、2012年产业平均耗水率为46%,上海市、江苏省等省市产业排水量下降趋势明显.②规模效应是驱动各省市产业排水增加的主要因素,其在2002—2007年、2007—2012年带动排水量分别增长了67%和61%;规模效应影响逐渐分化,上海市、江苏省、浙江省规模效应带动产业排水量增幅逐渐减弱.③节水减排效应是驱动排水量减少的最主要因素,其在2002—2007年、2007—2012年带动排水量分别减少了35%和60%,节水减排效应影响逐渐增强,各省市排水强度明显降低.④长江经济带大部分省市的需求结构效应驱动产业排水量不断减少,其驱动力的绝对值呈增长趋势;投入结构效应对产业排水量的驱动力较弱且变化规律性不明显.建议长江经济带通过技术进步、应用创新等提高清洁生产能力,通过需求及投入结构优化带动产业结构调整,对进一步降低产业排水量具有一定价值.