O3/GAC-常规处理珠江水系不同原水简

以东江、西江和北江3种原水为研究对象,采用臭氧预处理-常规处理-臭氧活性炭系列处理,研究原水中有机物的去除及臭氧化副产物的产生和转化。结果表明,东江、西江和北江水中COD_Mn、UV₂₅₄、甲醛和溴酸盐沿各处理单元过程变化规律基本一致;COD_Mn总去除率分别为60%、51%和39%,UV₂₅₄总去除率分别为74%、96%和97%,最终出水甲醛浓度分别为0.004 mg/L、0 mg/L和0 mg/L,BrO₃^-分别为3.1 μg/L、8.7 μg/L和35.5 μg/L;COD_Mn的去除主要在预臭氧和活性炭过滤2个处理单元,预臭氧对UV₂₅₄总去除率贡献最大,甲醛和溴酸盐浓度在主臭氧处理单元达到其峰值（西江甲醛除外）;氨氮和有机物浓度较低、pH值较高的北江原水,出水溴酸盐浓度最高。     

Knowledge-based system,equipped with cluster analysis for eco-material selection: an automobile structure case study

The aim of this study is to develop a material selection framework structured around a knowledge-based system (KBS). Specifically, a hybrid data mining technique is employed to extract knowledge from large datasets using cluster analysis techniques; the mined knowledge then serves as the inference logic within the KBS designed for material selection purposes. Cluster analysis results are used as a basis for the tree-based structure of the KBS where if–then rules are developed based on the general cluster properties; that is, inference logic is structured in a way such that it can predict general sustainability characteristics of the material as well as its exact mechanical, cost and physical properties. To develop the structure of the KBS, the selection structure employs sustainable material indices. Additionally, the proposed material selection model of the KBS is purposefully composed of material sustainability, functionality and cost indices. The constructed knowledge is then demonstrated for selecting automobile structural panels.     

Enhancement of phosphorus sorption onto light expanded clay aggregates by means of aluminum and iron oxide coatings

Phosphorus (P) loading from non-point or point sources increases the eutrophication risk of natural waters. The functioning of constructed wetlands (CWs) used as natural water treatment systems can be improved by means of additional materials adsorbing soluble P. In this study, light expanded clay aggregates (LECA) and LECA coated with aluminum (Al) oxide (Al-LECA) or iron (Fe) oxide (Fe-LECA) were tested for their efficiency as P sorbents in the pH range 3–8. The oxide coatings duplicated the actual sorption capacity calculated from the sorption isotherms at the P concentration in the equilibrium solution of 20 μg L⁻¹, assumed to be the allowable P level in purified water. In the oxide-coated LECAs the sorption was fast and followed both the first- and second-order Lagergren kinetic models, suggesting that the formation of a binuclear surface complex was feasible. In LECA, sorption was markedly slower and followed the first-order kinetic model, indicating that retention occurred through a monodentate attachment. These findings were in harmony with the degree of P saturation (DPS) of the sorbent surfaces at the highest P addition level (200 μg L⁻¹), DPS being decisively higher for LECA than for the oxide-coated sorbents. Accordingly, at higher pH values the competition by hydroxyl ions diminished the sorption in LECA relatively more than that in the coated sorbents. In agreement with the acidity of Al³⁺ being 100 times lower than that of Fe³⁺, at elevated pH the sorption by Al-LECA proved to be less reversible than that by Fe-LECA. The results provide evidence that in CWs Al-coated sorbents are superior to Fe-coated ones that are also redox-sensitive and may lose their sorption properties in anoxic conditions.     

Evaluating Controlling Factors to Ali/(Ca + Mg) Molar Ratio in Acidic Soil Water, Southern and Southwestern China: Multivariate Approach

Al_i/(Ca + Mg) molar ratio in soil water has been used as an indicator to the effects of acid deposition on terrestrial ecosystems. However, the main factors controlling this ratio have not been well documented in southern and southwestern China. In this study, we presented the variation in inorganic aluminum (Al_i) and Al_i/(Ca + Mg) molar ratio in different sites and soil horizons based on two to three years monitoring data, and evaluated the main factors controlling Al_i/(Ca + Mg) molar ratio using principle component analysis (PCA) and partial least square (PLS) regression. Monitoring data showed although Al_i/(Ca + Mg) molar ratios in most soil water were lower than assumed critical 1.0, higher molar ratios were found in some soil water at TSP and LXH site. Besides acid loading, both soil properties and soil water chemistry affected the value of Al_i/(Ca + Mg) molar ratio in soil water. Partial least square (PLS) indicated that they had different relative importance in different soil horizons. In A-horizon, soil aluminum saturation (AlS) had higher influence on Al_i/(Ca + Mg) molar ratio than soil water chemistry did; higher soil aluminum saturation (AlS) led to higher Al_i/(Ca + Mg) molar ratio in soil water. In the deeper horizons (i.e., B₁-, B₂- and BC-horizon), inorganic aluminum (Al_i) in soil water had more and more important role in regulating Al_i/(Ca + Mg) molar ratio. On regional scale, soil aluminum saturation (AlS) as well as cation exchange capacity (CEC) was the dominant factor controlling Al_i/(Ca + Mg) molar ratio. This should be paid enough attention on when making regional acid rain control policy in China.     

Simulated Effects of Acidic Solutions on Element Dynamics in Monsoon Evergreen Broad-leaved Forest at Dinghushan,China - Part 1: Dynamics of K,Na, Ca,Mg and P (7 pp)

Background, Aim and Scope Acid deposition has become a concern in south China in recent years. This phenomenon has increased to a dramatic extent with the large use of cars and coal- fueled power plants. As a consequence, soils are becoming acidified and their element dynamics will change. A decrease in the nutrient availability will lead to slower plant growth and maybe to a change in the forest type with current species being replaced by new ones with less nutrient requirements. Because of these reasons, it is important to understand how the dynamics of elements will change and what mechanism is part of the process. This knowledge is important for modeling the acidification process and either finding ways to counter it or to predict its consequences. The primary purpose of this study was to provide information about how the dynamics of K, Na, Ca, Mg and P are affected by acid deposition in a typical forest in southern China. Materials and Methods: Experimental soils and saplings were collected directly from the monsoon evergreen broad-leaved forest in Dinghushan. All saplings were transplanted individually into ceramic pots in August 2000 and placed in an open area near their origin site. Pot soils were treated weekly from October, 2000 to July, 2002 with an acidic solution at pH 3.05, pH 3.52, pH 4.00 or pH 4.40, or with tap water as a control. The concentrations of SO42-, NO3-, K+, Na+, Ca2+, Mg2+ and available P and the pH were measured in soil and leachate samples taken at different times. The sapling leaves were collected and their element concentrations were measured at the end of the experiment. Results: Concentrations of soil exchangeable Ca and Mg decreased quickly over time, although only Ca showed changes with the acidic solution treatment and soil exchangeable K was stable because of soil weathering. Leaching of K, Mg and Ca was dependent upon the treatment acidity. Soil available P decreased slowly without any correlation with the acidity of the treatment. All the NO3- added by the treatment was taken up by the plants, but the SO42- added accumulated in the soil. Discussion: Amongst the plant species, Schima superba was little affected by the treatment, the leaf P content was affected in Acmena acuminatissima plants and Cryptocarya concinna was the most susceptible species to soil acidification, with a marked decrease of the leaf K, Ca and Mg concentrations when the treatment acidity increased. Conclusions: Simulated acid deposition affected the dynamics of K, Ca and Mg in the monsoon evergreen broad-leaved forest. The dynamics of Ca in the soil and of K, Mg and Ca in the soil leachates were affected by the acidic solution treatment. If such a soil acidification occurs, Cryptocarya concinna will be amongst the first affected species, but Schima superba will be able to sustain a good growth and mineral nutrition. Recommendations and Perspectives: Acid deposition will lead to imbalance the nutrient elements in the evergreen broad-leaved forest because of accelerated leaching losses of soil exchangeable Ca and Mg. Measures should be developed to slow down soil acidification or nutrient decrease.     

57种臭氧前体有机物混合标准气体量值比对研究

标准物质的量值准确性是监测数据准确的重要前提。为科学评价57种臭氧前体有机物混合标准气体量值的准确性,研究建立了定量环进样-中心切割-气相色谱-双火焰离子化检测器分析方法与量值比对方法(E_n值法),并对市售6个品牌各2个批次标准气体开展量值比对研究。研究结果表明,4个品牌标气量值一致性、准确性较好,2个品牌存在5～22种组分量值偏离(E_n绝对值为1.0～5.3),用于开展臭氧前体有机物监测的标准物质质量仍需持续监督、提升。     

纳米材料在痕量重金属离子测定中的应用

介绍了纳米材料的吸附性能,评述了影响其分离富集重金属离子效果的主要因素,综述了纳米金属氧化物、碳纳米管及其他纳米材料在痕量重金属离子测定中的应用进展,提出提高纳米吸附材料的选择性和稳定性,开发便携式商品化的纳米材料萃取小柱是今后的发展方向.     

珠江三角洲制鞋行业挥发性有机化合物排放系数研究

采用工艺调查与现场监测相结合的方法,以物料衡算法为依据,通过现场监测结果进行验证,研究了制鞋行业挥发性有机化合物(VOCs)排放系数。结果表明,水性胶粘剂使用企业的VOCs排放系数为(5.25±2.67)g/双,油性胶粘剂使用企业的VOCs排放系数为(30.11±10.60)g/双,根据不同类型胶水在制鞋行业中所占的权重,可得到反映地方特色的制鞋行业VOCs排放系数。     

自制模拟样及留样复测的质控技术探讨

介绍了环境监测标准滤膜、标准滤筒、模拟降尘的制备方法、使用方法、实际效果。阐述了滤膜中铅、土壤样品、底泥（沉积物）、污水厂处理污泥等留样的来源、必要性及作用。探讨了滤膜中铅留样复测质控的评判依据。     

工业链条炉燃用型煤与原煤颗粒物排放特征

选取燃烧型煤和原煤的典型链条炉,应用自行设计的固定源烟气颗粒物稀释采样系统,现场测试细颗粒物PM_(2.5)、PM_(10)和金属元素的排放特征。结果表明,型煤燃烧细颗粒物的排放比例高于原煤,型煤燃烧除尘器进口、出口PM_(2.5)质量比原煤燃烧分别增加715%和708%。燃烧型煤时,As和Pb在各粒径段的质量比均比原煤大。同时,由于型煤燃烧可吸入颗粒物的排放比例增加,包含或附着在烟尘上的金属元素排放比例也相应增加。