Catalytic degradation of toxic organic dye using an aluminum-doped Cu0.4Zn0.6-xAlxFe2O4 (x = 0.0, 0.2, 0.4, 0.6) spinel ferrite in a photo-Fenton system

Catalytic activity of spinel ferrite in breaking down toxic dye materials are promising due to their uniqueness. In this study, aluminum-doped copper zinc ferrite, Cu_0.4Zn_0.6-xAl_xFe₂O₄ (x = 0.0, 0.2, 0.4, 0.6), a catalyst for toxic dye degradation is synthesized through chemical co-precipitation route. The formation of the spinel ferrite catalyst is initially confirmed by Fourier transform infrared spectra, which shows the frequency of metal-oxygen bond vibration at 539 and 427 cm⁻¹ attributed to the tetrahedral and octahedral sites respectively. Higher intensity sharp peak of X-ray diffraction for (311) plane is the evidence for the phase purity and the formation of spinel ferrite. The crystallite size is found to decrease with the increase of Al³⁺ ion. The surface structure of the obtained particles is investigated using a scanning electron microscope. Analyses of the material's magnetic characteristics using a vibrating sample magnetometer (VSM) revealed that it is, in fact, a soft magnet, as evidenced by the loop of its hysteresis, which is narrow. The catalytic degradation of methylene blue dye under the mechanism of the photo-Fenton process is studied with the obtained spinel ferrites and the result is found to be as high as 96.5%. The process follows pseudo-second order kinetics and the Langmuir isotherm.     

Evaluation of photolysis and hydrolysis of pyraclostrobin in aqueous solutions and its degradation products in paddy water

This study evaluated the hydrolysis and photolysis kinetics of pyraclostrobin in an aqueous solution using ultra-high-performance liquid chromatography–photodiode array detection and identified the resulting metabolites of pyraclostrobin by hydrolysis and photolysis in paddy water using high-resolution mass spectrometry coupled with liquid chromatography. The effect of solution pH, metal ions and surfactants on the hydrolysis of pyraclostrobin was explored. The hydrolysis half-lives of pyraclostrobin were 23.1–115.5?days and were stable in buffer solution at pH 5.0. The degradation rate of pyraclostrobin in an aqueous solution under sunlight was slower than that under UV photolysis reaction. The half-lives of pyraclostrobin in a buffer solution at pH 5.0, 7.0, 9.0 and in paddy water were less than 12?h under the two light irradiation types. The metabolites of the two processes were identified and compared to further understand the mechanisms underlying hydrolysis and photolysis of pyraclostrobin in natural water. The extracted ions obtained from paddy water were automatically annotated by Compound Discoverer software with manual confirmation of their fragments. Two metabolites were detected and identified in the pyraclostrobin hydrolysis, whereas three metabolites were detected and identified in the photolysis in paddy water.     

废旧硬质聚氨酯泡沫塑料的木质素改性及再生

采用含有二乙二醇(DEG)和乙醇胺(ETA)的双组分解交联剂降解废旧硬质聚氨酯泡沫塑料(PU硬泡),并利用降解得到的低聚物多元醇与木质素复合制备出性能增强的再生PU硬泡。通过对制备的再生PU硬泡的红外光谱、密度、吸水率、抗压强度、热稳定性、导热系数、热重曲线等进行分析测试,考察m(DEG)∶m(ETA)对再生PU硬泡性能的影响。实验结果表明:m(DEG)∶m(ETA)=1∶3时废旧PU硬泡的降解效果最好;木质素加入量为2.0%(w)时再生PU硬泡的密度低、抗压强度高、保温性能良好,达到国家标准《建筑绝热用硬质聚氨酯泡沫塑料》(GB/T 21558—2008)的品质要求。     

Eco-Environmental Degradation in the Source Region of the Yellow River, Northeast Qinghai-Xizang Plateau

The Yellow River is the second longest river in China and the cradle of the Chinese civilization. The source region of the Yellow River is the most important water holding area for the Yellow River, about 49.2% of the whole runoff comes from this region. However, for the special location, it is a region with most fragile eco-environment in China as well. Eco-environmental degradation in the source region of the Yellow River has been a very serious ecological and socially economic problem. According to census data, historical documents and climatic information, during the last half century, especially the last 30 years, great changes have taken place in the eco-environment of this region. Such changes are mainly manifested in the temporal-spatial changes of water environment, deglaciation, permafrost reduction, vegetation degeneracy and desertification extent, which led to land capacity decreasing and river disconnecting. At present, desertification of the region is showing an accelerating tendency. This paper analyzes the present status of eco-environment degradation in this region supported by GIS and RS, as well as field investigation and indoor analysis, based on knowledge, multi-source data is gathered and the classification is worked out, deals with their natural and anthropogenic causes, and points out that in the last half century the desertification and environmental degradation of this region are mainly attributed to human activities under the background of regional climate changes. To halt further degradation of the environment of this region, great efforts should be made to use land resources rationally, develop advantages animal agriculture and protect the natural grassland.     

Changes Of Hydrological Environment And Their Influences On Coastal Wetlands InThe Southern Laizhou Bay, China

The structure and function of the coastal wetland ecosystem in the southern Laizhou Bay have been changed greatly and influenced by regional hydrological changes. The coastal wetlands have degraded significantly during the latest 30 years due to successive drought, decreasing of runoff, pollution, underground saline water intrusion, and aggravating marine disasters such as storm tides and sea level rising. Most archaic lakes have vanished, while artificial wetlands have been extending since natural coastal wetlands replaced by salt areas and ponds of shrimps and crabs. The pollution of sediments in inter-tidal wetlands and the pollution of water quality in sub-tidal wetlands are getting worse and therefore “red tides” happen more often than before. The biodiversity in the study area has been decreased. Further studies are still needed to protect the degraded coastal wetlands in the area.     

社会和谐与可持续发展

本文运用系统科学原理阐释了社会和谐的内涵,指出社会和谐须以人与自然和谐为基础,以人与人之间的平等、友爱和同合作为表征,其构建与实现应遵从人类社会的演化规律,依赖予在把握人类社会需求演绎、协同人与自然关系的基础上推动生产力的高效有序发展和自然资源、生态环境的可持续支持.进而从可持续发展角度,提出了人与自然和谐的"双剩余理论",以揭示其间的供瓣枧理和协同准则;推导出了社会收益分配的相对公平系数,以衡量人与人公平要求下的社会和谐.针对国情和战略目标要求,提出了以加强小城镇建设为轴心的城市、小城镇与农村人流、物流、财流和信息流合理聚散的"三元结构"发展模式,以促进我国和谐社会的建设和可持续发展战略的有序实践.     

Estimation of Land Use Specific Runoff and Pollutant Concentration for Tapi River Basin in India

Non-point source (NPS) pollution is the result of various land use practices such as agriculture, sites of construction and waste disposal, urban development and so on. The control of NPS pollution is possible by regular monitoring and assessment on watershed basis to educate people for implementing well-known structural and non-structural measures. Recent trend is to use GIS based modelling tool for assessment of rainfall-runoff and non-point loading. The approach requires generation and analysis of basin wide data on various features of land and estimates of Event Mean Concentrations (EMCs) of pollutants in the runoff. In the present paper, basin wide data in different districts of Tapi basin has been analysed for land use distribution; fertilizer application; low, medium and high-density habitation; and annual rainfall. Coefficients of runoff have been estimated considering pervious and impervious area for different land use types, and compared with the reported values for Indian conditions. The estimated mean annual runoff flow indicated that two districts Jalgaon and Dhule contribute maximum runoff to the Tapi River. Estimates of EMCs for BOD and nutrients (N and P) in the runoff from various districts are useful in GIS-based modelling study for NPS pollution assessment.     

粤港澳大湾区NO2污染的时空特征及影响因素分析

利用Aura卫星搭载的臭氧观测仪（OMI）反演的对流层NO₂柱密度数据,分析了自2005年以来粤港澳大湾区（GBA）对流层NO₂柱密度的空间分布特征、时间变化趋势及其影响因素.研究结果表明GBA对流层NO₂柱密度从2005~2018年呈减少的趋势,每年递减约为2.8%.小波系数显示时间演化过程中存在9个月的主振荡周期,冬季浓度较高,夏季较低.人为排放和各种自然因素,导致了GBA对流层NO₂柱浓度月变化在时间和空间上存在明显差异,最小值和最大值分别出现在6和12月,多年平均值分别为3.9665×10¹⁵和12.3423×10¹⁵molec/cm².NO₂在空间分布上呈现明显的空间分异特征,冬季12月最明显.NO₂污染严重的高值区主要出现在中部地区,如广州市、佛山市和中山市,最大的对流层NO₂柱密度可达18.8306×10¹⁵molec/cm²,大约是周边地区的3 倍,且高污染区域向四周逐渐扩散,连成一片.低值区主要在北部的肇庆市和东部的惠州市,多年平均的对流层NO₂柱密度约为7.1400×10¹⁵molec/cm².对流层NO₂柱密度的增长率在不同区域的变化趋势呈现明显的差异,变化范围为-15×10¹⁵~6×10¹⁵molec/cm²,增长率百分比范围为-65%~65%.出现增长的地区主要是肇庆市北部和惠州市东部的低值区;对流层NO₂出现明显减少的区域集中在中部的高值区,减少量最大的地区为广州市、佛山市和中山市交界处.     

二溴硝基甲烷在紫外光照条件下的光降解

以二溴硝基甲烷为研究,采用单一控制变量法研究了光照强度、初始物浓度、自由氯、溴离子、pH值等影响因子对二溴硝基甲烷光降解的影响,探讨了二溴硝基甲烷的光降解动力学规律.结果表明：二溴硝基甲烷在紫外光条件下的降解遵循一级反应动力学规律,其光降解效率随二溴硝基甲烷初始浓度的增加而减小,随光照强度和pH值增加而增加;溴离子的存在能促进二溴硝基甲烷的光降解;添加自由氯能够显著加快二溴硝基甲烷的光降解效率,并且会使二溴硝基甲烷在光降解的过程中转化为以一溴一氯硝基甲烷为主的其他卤代硝基甲烷.此研究结果可为水处理过程中控制二溴硝基甲烷的形成、降低水质安全风险提供参考.     

Effect of substituents in hydroxyl radical-mediated degradation of azo pyridone dyes: Theoretical approaches on the reaction mechanism

Understanding the degradation behavior of azo dyes in photocatalytic wastewater treatment is of fundamental and practical importance for their application in textile-processing and other coloration industries. In this study, quantum chemistry, as density functional theory, was used to elucidate different degradation pathways of azo pyridone dyes in a hydroxyl radical (HO^?)-initiated photocatalytic system. A series of substituted azo pyridone dyes were synthesized by changing the substituent group in the para position of the benzene moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The effect of dye molecular structure on the photocatalytic degradation reaction mechanism was analyzed and quantification of substituent effects on the thermodynamic and kinetics parameters was performed. Potential energy surface analysis revealed the most susceptible reaction site for the HO^? attack. The calculated reaction barriers are found to be strongly affected by the nature of substituent group with a good correlation using Hammett σ_p constants and experimentally determined reaction rates. The stability of pre-reaction complexes and transition state complexes were analyzed applying the distortion-interaction model. The increased stability of the transition state complexes with the distancing from the substituent group has been established.