LPWCO method for the treatment of high concentrated organic wastewater

Based on wet air oxidation (WAO) and Fenton reagent, thispaper raises a new low pressure wet catalytic oxidation(LPWCO)which requires low pressure for the treatment of highlyconcentrated and refractory organic wastewater. Compared withgeneral wet air oxidation, the pressure of the treatment(0.1-0.6MPa) is only one of tens to percentage of latter(3.5-10MPa). Inaddition, its temperature is no more than 180℃.Compared withFenton reagent, while H2O2/COD(weight ratio) less than 1.2, theremoval of COD in the treatment is over twenty percents more thanFenton's even the value of COD is more than 14000mg/L. In thispaper, we study the effect factor of COD removal and the mechanismof this treatment. The existence of synergistic effect (catalytic oxidation and carbonization) for COD removal in H2SO4-Fenton reagent system under the condition of applied pressure and heating (0.1-0.6MPa, 104-165℃) was verified. The best condition of this disposal are as follows:H2O2/COD(weight ratio)=0.2-1.0, Fe2+ 0.6×10-3 mol, H2SO4 0.5mol, COD>1×104mg/L, the operating pressure is 0.1-0.6MPa and temperature is 104-165℃. This method suit to dispose the high-concentrated refractory wastewater, especially to the wastewater containing H2SO produced in the manufacture of pesticide, dyestuff and petrochemical works.     

生态技术创新政府启动模式的机理与启示

生态技术创新是经济可持续发展的必要条件。由于环境资源的公共性，时滞性等特点，政府在生态技术创新过程中发挥重要的作用，是企业生态技术创新的主要推动力。政府启动模式的本 于政府借助法律或经济手段促使企业部分边际外部费用内部化。     

用等维灰色动态预测法预测大连湾污染物排放量

用少量数据建立的长期预测模型所得预测结果一出散性较大，本文介绍的等维灰色动态预测去弥补了这一缺陷。依据这一方法编制的“灰色原理应用系统”软件包，在获得预测结果的同时，还可得到预测值的变化过程及模型的相应参数，可即时对预测结果的可靠性作出判断。     

抓源头治理是落实“两控区”2000年初期目标的优先选择

针对我国煤中硫分赋存状况,抓源头治理,分别对高硫煤,中硫煤和低硫煤采取不同对策,切实有效地实现“两控区”２０００年的初期目标。     

南昌市冬季大气PM2.5中重金属元素来源分析及健康风险评价

采集2015年南昌市冬季大气PM_(2.5)样品,利用电感耦合等离子体质谱仪(ICP-MS)测定样品中重金属(V、Mn、Cr、Co、Ni、Cu、Zn、Cd、Ba和Pb)的含量,分析重金属的分布特征和来源,并对重金属健康风险进行评价。结果表明:采样期间PM2.5浓度总平均值为(29.74±16.82)μg/m~3,其中省外办最高,武术学校最低;各重金属元素总体平均浓度从高到低次序为:ZnPbCuMnBaNiVCrCdCo。因子分析结果表明:PM_(2.5)中重金属元素的来源包括道路交通尘和冶金化工排放、机动车尾气以及混合源。健康风险评价结果显示:PM_(2.5)中Mn对人体健康存在非致癌风险,其他元素(Cr、Ba、Co、Pb、Cd、Cu、V、Zn、Ni)基本没有非致癌风险;Cr对人体有较明显的致癌风险,Cd、Ni和Co对部分年龄段的人群(尤其是成年人)存在一定的致癌风险。     

Regionalization based on spatial and seasonal variation in ground-level ozone concentrations across China

Owing to the vast territory of China and strong regional characteristic of ozone pollution,it's desirable for policy makers to have a targeted and prioritized regulation and ozone pollution control strategy in China based on scientific evidences. It's important to assess its current pollution status as well as spatial and temporal variation patterns across China.Recent advances of national monitoring networks provide an opportunity to insight the actions of ozone pollution. Here, we present rotated empirical orthogonal function(REOF)analysis that was used on studying the spatiotemporal characteristics of daily ozone concentrations. Based on results of REOF analysis in pollution seasons for 3 years' observations, twelve regions with clear patterns were identified in China. The patterns of temporal variation of ozone in each region were separated well and different from each other, reflecting local meteorological, photochemical or pollution features. A rising trend in annual averaged Eight-hour Average Ozone Concentrations(O_3-8 hr) from 2014 to 2016 was observed for all regions, except for the Tibetan Plateau. The mean values of annual and 90 percentile concentrations for all 338 cities were 82.6 ± 14.6 and 133.9 ± 25.8 μg/m~3,respectively, in 2015. The regionalization results of ozone were found to be influenced greatly by terrain features, indicating significant terrain and landform effects on ozone spatial correlations. Among 12 regions, North China Plain, Huanghuai Plain, Central Yangtze River Plain, Pearl River Delta and Sichuan Basin were realized as priority regions for mitigation strategies, due to their higher ozone concentrations and dense population.     

基于计算模拟与响应面分析漆酶对己烯雌酚的降解作用

己烯雌酚(Diethylstilbestrol,DES)作为水环境中最具雌激素活性的合成化合物之一,其给生物体和环境带来的危害已经引起人们的关注.本研究首先通过分子对接与分子动力学模拟从理论上分析漆酶与DES的相互作用;其次通过实验分析其降解动力学模型及不同反应条件和介质对漆酶催化转化DES的影响;最后使用响应面分析方法优化漆酶-ABTS系统催化转化DES的最佳条件.计算结果表明,漆酶与DES的反应能够自发进行且它们之间主要存在氢键和疏水作用力.实验结果表明,反应6 h左右,50 mg·L^-1的DES的降解率达到93%以上;根据Michaelis-Menten模型得到的动力学参数K_m和V_max分别为36.18 mg·L^-1和45.98 mg·L^-1·h^-1,模型的R²为0.99.漆酶催化降解DES的最佳pH为6,最佳温度为55℃.几种介质中,ABTS对漆酶催化降解DES的作用最强.通过响应面分析发现,在pH=5.5、55.98℃、1....     

Hygroscopicity measurement of sodium carbonate, β-alanine and internally mixed β-alanine/Na2CO3 particles by ATR-FTIR

Water-uptakes of pure sodium carbonate(Na_2CO_3),pure β-alanine and internally mixedβ-alanine/Na_2CO_3 aerosol particles with different mole ratios are first monitored using attenuated total reflectance Fourier transform infrared spectroscopy(ATR-FTIR) technique.For pure Na_2CO_3 aerosol particles,combining the absorptions at 877 and 1422 cm-1 with abrupt water loss shows the efflorescence relative humidity(ERH) of 62.9%–51.9%.Upon humidifying,solid Na_2CO_3 firstly absorbs water to from Na_2CO_3·H2 O crystal at 72.0% RH and then deliquesces at 84.5% RH(DRH).As for pure β-alanine particles,the crystallization takes place in the range of 42.4%–33.2% RH and becomes droplets at ～ 88.2% RH.When β-alanine is mixed with Na_2CO_3 at various mole ratios,it shows no efflorescence of Na_2CO_3 whenβ-alanine to Na_2CO_3 mole ratio(OIR) is 2:1.For 1:1 and 1:2 β-alanine/Na_2CO_3 aerosols,the ERHs of Na_2CO_3 are 51.8%–42.3% and 57.1%–42.3%,respectively.While β-alanine crystal appears from 62.7% RH for 2:1 and 59.4% RH for both 1:1 and 1:2 particles and lasts to driest state.On hydration,the DRH is 44.7%–75.2% for Na_2CO_3 with the OIR of 1:1 and 44.7%–69.0%for 1:2 mixture,and those of β-alanine are 74.8% for 2:1 mixture and 68.9% for two others.After the first dehumidification–humidification,all the water contents decrease despite of constituent fraction.And at ～ 92% RH,the remaining water contents are 92%,89% and 82%at ～ 92% RH,corresponding to OIR of 2:1,1:1 and 1:2 mixed system,respectively.     

Layered sphere-shaped TiO2 capped with gold nanoparticles on structural defects and their catalysis of formaldehyde oxidation

We describe here a one-step method for the synthesis of Au/TiO₂ nanosphere materials, which were formed by layered deposition of multiple anatase TiO₂ nanosheets. The Au nanoparticles were stabilized by structural defects in each TiO₂ nanosheet, including crystal steps and edges, thereby fixing the Au–TiO₂ perimeter interface. Reactant transfer occurred along the gaps between these TiO₂ nanosheet layers and in contact with catalytically active sites at the Au–TiO₂ interface. The doped Au induced the formation of oxygen vacancies in the Au–TiO₂ interface. Such vacancies are essential for generating active oxygen species (*O⁻) on the TiO₂ surface and Ti^3 + ions in bulk TiO₂. These ions can then form Ti^3 +–O⁻–Ti^4 + species, which are known to enhance the catalytic activity of formaldehyde (HCHO) oxidation. These studies on structural and oxygen vacancy defects in Au/TiO₂ samples provide a theoretical foundation for the catalytic mechanism of HCHO oxidation on oxide-supported Au materials.