pH值对氨氮电化学氧化产物与氧化途径的影响

摘要:研究了含氨氮废水在循环流动式电解槽中的电化学氧化,讨论了pH值对氨氮电化学氧化效果、产物及其途径的影响。结果表明,在弱碱性条件下,有利于电解过程中羟基自由基和游离氯的生成,氨氮的电化学氧化速率较大。在有氯离子存在的情况下,氨氮电化学氧化过程中有氯胺生成,氯胺的组成与体系的pH值有关,当pH>9时,一氯胺占优势;当pH=7时,一氯胺和二氯胺同时存在,并且近似相等;当pH<5时,主要是二氯胺;pH值大于5时,可以避免三氯化氮的生成。在电流密度为20mA/cm2时,电解产生的羟基自由基小于5×10-15mol/L,氨氮电化学氧化的2种途径中间接氧化起主要作用。     

重庆的国家重点保护植物研究

基于《中国植物红皮书》第一、二册名录，重庆有国家重点保护植物７７种，隶属于４７科，７１属。根据第一批公布的国家重点保护植物，重庆有５２种４９属３２科；其中一级５种，二级２４种，三级２３种，濒危６种，稀有２１种，渐危２５种。水平分布有三个中心，即大巴山南缘地区、武陵山区、大娄山北缘地区。论文最后提出了珍稀濒危植物的保护措施。     

生活与工业污水混合处理系统中关键毒物追踪

以常州市城北污水处理厂的进水和A^2O出水为研究对象，采用毒性鉴别评价（T IE）程序，对关键毒物进行了追踪。结果表明，进水对大型蚤（Daphnia magna）具 有24h急性毒性，经过A^2O系统的处理，出水已不显示24h急性毒性；因曝气可去除废水毒性，C18固相提取亦可去除废水毒性，据此判断进水中存在的主要毒物 为挥发性非极性有机化合物。进出水的GC／MS图谱显示，处理前后有机物浓度大大降低，关键毒物基本去除。     

城市污水处理BOT模式的几个关键问题

基于BOT模式系统分析,识别3大类8个关键问题:①政策方面,包括土地使用权、政府补偿、产权;②投资与建设方面,工艺前瞻性、风险、管网配套;③运营与保障方面,包括收费定价、回报率,并在此基础上探讨城市污水处理BOT模式,为我国BOT模式的开展提供决策支持。     

Is the environment becoming more hazardous?—A global survey 1947 to 1980

This paper examines the assertion that natural disasters are increasingly destructive using evidence from disaster reports during the period 1947–1980. The criteria for judging the impact of a given natural disaster are chiefly loss of life and the extent of the geographical area affected. In spite of uneveness and bias in the reporting of sudden impact disasters the conclusions are that both the frequency of disasters and number of people killed are increasing. Further research into the social consequences of disasters and the need for disaster preparedness training programmes are recommended.     

The tragedy of Kampuchea

This paper, abstracted from the final report of the Kampuchea Inquiry Commission, analyses the population losses in Cambodia prior to 1979 and goes on to describe some of the unwanted side effects of the international relief programmes in both Thailand and in Kampuchea. The paper concludes that various opposition movements to the present Vietnamese backed regime in Kampuchea have been strengthened by international aid.     

Aftermath of natural disasters: Coping through residential mobility

Most studies of population movement have concentrated on the more developed nations and on trends that have not been influenced by man-made or natural disasters. The experience of developing countries in the Caribbean basin, as studied after the Guatemalan earthquake of 1976 and the impact of Hurricane David in the Dominican Republic of 1979, highlights the importance of socio-economic factors in the decision to make permanent migrations after a disaster, regardless of whether the migrant had personally suffered losses. In many cases the opportunities for personal betterment created by the disaster acted as a catalyst and accelerated a previously-existing trend of migration.     

Vertical profiles of biogenic volatile organic compounds as observed online at a tower in Beijing

Vertical profiles of isoprene and monoterpenes were measured by a proton transfer reaction-time of flight-mass spectrometry (PTR-ToF-MS) at heights of 3, 15, 32, 64, and 102 m above the ground on the Institute of Atmospheric Physics (IAP) tower in central Beijing during the winter of 2016 and the summer of 2017. Isoprene mixing ratios were larger in summer due to much stronger local emissions whereas monoterpenes were lower in summer due largely to their consumption by much higher levels of ozone. Isoprene mixing ratios were the highest at the 32 m in summer (1.64 ± 0.66 ppbV) and at 15 m in winter (1.41 ± 0.64 ppbV) with decreasing concentrations to the ground and to the 102 m, indicating emission from the tree canopy of the surrounding parks. Monoterpene mixing ratios were the highest at the 3 m height in both the winter (0.71 ± 0.42 ppbV) and summer (0.16 ± 0.10 ppbV) with a gradual decreasing trend to 102 m, indicting an emission from near the ground level. The lowest isoprene and monoterpene mixing ratios all occurred at 102 m, which were 0.71 ± 0.42 ppbV (winter) and 1.35 ± 0.51 ppbV (summer) for isoprene, and 0.42 ± 0.22 ppbV (winter) and 0.07 ± 0.06 ppbV (summer) for monoterpenes. Isoprene in the summer and monoterpenes in the winter, as observed at the five heights, showed significant mutual correlations. In the winter monoterpenes were positively correlated with combustion tracers CO and acetonitrile at 3 m, suggesting possible anthropogenic sources.     

Simultaneous removal and oxidation of arsenic from water by δ-MnO2 modified activated carbon

The ubiquitous arsenic in groundwater poses a great risk to human health due to its environmental toxicity and carcinogenicity. In the present work, a new adsorbent, δ-MnO₂ modified activated carbon, was prepared, and its performance for the uptake of arsenate and arsenite species from aqueous solutions was investigated by batch experiments. Various techniques, including FESEM-EDX, p-XRD, XPS and BET surface area analysis, were employed to characterize the properties of the adsorbent and the arsenic adsorption mechanisms. The results showed that δ-MnO₂ covered on the surface and padded in the pores of the activated carbon. Adsorption kinetic studies revealed that approximately 90.1% and 76.8% of As(III) and As(V), respectively, were removed by the adsorbent in the first 9 hr, and adsorption achieved equilibrium within 48 hr. The maximum adsorption capacities of As(V) and As(III) at pH 4.0 calculated from Langmuir adsorption isotherms were 13.30 and 12.56 mg/g, respectively. The effect of pH on As(V) and As(III) removal was similar, and the removal efficiency significantly reduced with the increase of solution pH. Arsenite oxidation and adsorption kinetics showed that the As(V) concentration in solution due to As(III) oxidation and reductive dissolution of MnO₂ increased rapidly during the first 12 min, and then gradually decreased. Based on the XPS analysis, nearly 93.3% of As(III) had been oxidized to As(V) on the adsorbent surface and around 38.9% of Mn(IV) had been reduced to Mn(II) after As(III) adsorption. This approach provides a possible method for the purification of arsenic-contaminated groundwater.     

长江经济带国家重点生态功能区生态补偿环境效率评价

环境效率是考量生态补偿政策实施效果的重要指标,对国家重点生态功能区生态补偿环境效率进行有效测度可以为完善我国生态补偿政策提供有益参考.采用三阶段DEA模型对长江经济带11个省市的国家重点生态功能区生态补偿环境效率水平、变化趋势及其差异性进行评价,通过线性数据转化方法对非期望环境负产出进行处理,并识别第三产业增加值占比等背景变量对投入产出效率的影响.结果表明:①长江经济带第三产业增加值占比对能源投入产出的影响显著（t值检验达到5%显著性水平）,进出口总额、人均GDP、人口密度等因素对各项投入产出的影响均不显著.②长江经济带11个省市2012-2017年综合技术效率均值在剔除背景因素和随机干扰前后未发生变化,但纯技术效率均值由调整前的0.94升至调整后的0.96,规模效率均值由调整前的0.94降至0.92,表明纯技术效率对提高环境效率起主导作用.③上游4个省市（重庆市、四川省、云南省、贵州省）与中下游7个省市（江西省、湖南省、湖北省、安徽省、江苏省、浙江省、上海市）生态补偿环境效率均值差距较大,其中,云南省的环境效率最低.研究显示,长江经济带11个省市的国家重点生态功能区生态补偿环境效率从上游到下游整体呈上升趋势,应在提高综合技术效率的同时,更加注重基本公共服务能力和生态环境保护双重目标的协调.