超滤膜深度处理染整废水的膜污染机理

实验采用不同规格和材料的超滤膜进行染整二级尾水分离实验,对超滤膜污染机理及影响因素进行了分析。实验采用红外光谱分析了聚醚(PES)膜、聚砜(PSF)膜和聚醚酰亚胺(PEI)膜3种超滤膜材料,对比了污染前后膜面的接触角以及不同切割分子量对膜通量及出水水质的影响,并利用线性化的Herman堵塞模型拟合了不同分子量超滤膜的堵塞模型,初步探讨了超滤膜的污染机理。实验结果表明,膜材料表面亲水性基团的多少与初始膜通量大小成正比,出水COD值随超滤膜切割分子量减小而减小。切割分子量同为2 000 Da的3种超滤膜中,PES膜的处理效果最佳,出水COD平均值为47.81 mg/L;PEI膜通量最高,平衡通量可达50 L/(m2.h);切割分子量为1 000、10 000的超滤膜堵塞机理符合滤饼过滤模型,100 000的超滤膜堵塞机理更接近于完全堵塞模型;1 000的聚醚砜材质膜(PES)更适合此类废水的深度处理。     

Even sampling designs generation by charges repulsion simulation

Evenly distributed sampling design is generally considered as an efficient sampling design. It is widely used in sampling for the environmental survey. In this paper, we present a novel method for generating N evenly distributed samples within a given irregular polygon via simulating the movements of some ideal homogeneous point charges. Initially, charges are randomly put into the sampling region; then, they are freed and held orderly; and after enough runs, the charges will finally reach a stable state with all of them having a zero resultant force and velocity; and so they distribute evenly within the region. Their layout can thus be considered as an evenly distributed sampling design. The main advantages of this method are: (1) it is easy to understand and implement; (2) it is efficient in both running and generating better designs. Analysis and experimental results indicate that this method is an efficient and robust method for generating even sampling designs for 2D polygonal sampling region.     

纳米ZnO/PS薄膜的制备及光降解性能

利用纳米ZnO与聚苯乙烯(PS)高速共混法制备了一种在紫外光下具有自降解性能的复合薄膜.分析表明,经过KH570处理的纳米ZnO与PS通过化学键的方式桥联在一起.TG分析表明,复合薄膜的耐热性较PS有所提高；SEM图像显示0.5 wt％ ZnO在PS薄膜表面分布均匀,经过UV照射后薄膜表面出现光腐蚀现象.复合薄膜紫外光自降解实验表明:0.5 wt％ ZnO/PS薄膜在15W的紫外灯照射下,15d的自降解率为3.715％.     

介质阻挡放电联合催化臭氧化降解甲苯

采用介质阻挡放电区后结合MnOx/Al2O3/发泡镍去除甲苯,考察甲苯进气方式、臭氧产生方法及湿度对甲苯与O3同时去除的影响。结果表明,O3是等离子体区后催化降解甲苯的主要物种,介质阻挡放电联合催化臭氧化可实现甲苯及O3的同时高效去除。输入电压为9.0 kV时,甲苯的去除效率达92.8%,在80 min内O3的去除效率维持在99%以上。水蒸气对催化剂催化分解臭氧的活性没有直接的影响,O3浓度较高时湿度对甲苯降解效率的影响很小。GC-MS分析结果表明,甲苯降解的主要气相副产物有烷烃、酸、酮和含苯环有机物,提出了甲苯的降解途径。     

Characteristic, composition, and sources of TSP investigated by HRTEM/EDS and ESEM/EDS

Total suspended particle (TSP) collected at the fifth floor of House Dust in Hunan University, China, was analyzed in terms of microscopic morphology and chemical composition. The fine particles (50?nm-2?μm) in the TSP were analyzed by a high-resolution transmission electron microscope equipped with an energy-dispersive X-ray analyzer (HRTEM/EDS). Results showed that the particles were in shapes of plate, irregular and agglomerate. Based on EDS results, these fine particulate matter was primarily composed of Fe-rich (35.82-61.29%), Ca-rich (30.18-36.77%) and Si-rich (18.95-32.28%) particles. Other elements mainly including Mg (0.47-4.97%), Al (0.45-14.57%), S (0.45-4.73%), K (1.13-2.13%) and Zn (0.67-3.85%) were also observed. The sources analysis indicated that the HRTEM particles mainly originated from coal combustion, traffic emission, vehicles exhaust emission and fugitive soil or cement particulate matter. The coarse particles (4-50?μm) were detected by environmental scanning electron microscopy coupled with energy-dispersive X-ray detector (ESEM/EDS). Based on a simple algorithm, ESEM particles were categorized into five groups: C-bearing (46.15%, 67% and 86.98%), Si + Ca-bearing (21.48?+?11.80%, 16.51?+?10.81% and 16.32?+?10.62%), Si + Al-bearing (20.06?+?12.40%, 20.16?+?11.22% and 15.31?+?11.25%), Si-bearing (34.40%, 26.92% and 27.15%) particles and aggregates, most of which exhibit obvious crystalline structure, and these ESEM particles mainly derived from vehicles exhaust emission, coal combustion, soil, and biomass burning, while the aggregates are indicative of atmospheric reaction progress. HRTEM/EDS and ESEM/EDS are mutual complementary in analyzing the characteristic and determining the sources of TSP.     

A new direct thermal desorption-GC/MS method: Organic speciation of ambient particulate matter collected in Golden, BC

Particulate matter having an aerodynamic diameter less than 2.5 μm (PM2.5) is thought to be implicated in a number of medical conditions, including cancer, rheumatoid arthritis, heart attack, and aging. However, very little chemical speciation data is available for the organic fraction of ambient aerosols. A new direct thermal desorption-gas chromatography/mass spectrometry (TD-GC/MS) method was developed for the analysis of the organic fraction of PM2.5. Samples were collected in Golden, British Columbia, over a 15-month period. n-Alkanes constituted 33–98% by mass of the organic compounds identified. PAHs accounted for 1–65% and biomarkers (hopanes and steranes) 1–8% of the organic mass. Annual mean concentrations were: n-alkanes (0.07–1.55 ng m⁻³), 16 PAHs (0.02–1.83 ng m⁻³), and biomarkers (0.02–0.18 ng m⁻³). Daily levels of these organics were 4.89–74.38 ng m⁻³, 0.27–100.24 ng m⁻³, 0.14–4.39 ng m⁻³, respectively. Ratios of organic carbon to elemental carbon (OC/EC) and trends over time were similar to those observed for PM2.5. There was no clear seasonal variation in the distribution of petroleum biomarkers, but elevated levels of other organic species were observed during the winter. Strong correlations between PAHs and EC, and between petroleum biomarkers and EC, suggest a common emission source – most likely motor vehicles and space heating.     

Carbon isotope analysis for source identification of atmospheric formaldehyde and acetaldehyde in Dinghushan Biosphere Reserve in South China

Formaldehyde and acetaldehyde are two most abundant carbonyls in ambient air. Biogenic emission has been proposed as a significant source other than anthropogenic emissions and atmospheric secondary formation. Here at a forest site in South China, the carbon isotopic compositions of formaldehyde and acetaldehyde emitted from leaves of three tree species (Litsea rotundifolia, Canarium album and Castanea henryi) were measured in comparison with the bulk carbon isotopic compositions of tree leaves. δ¹³C data of the emitted aldehydes (from ?31‰ to ?46‰) were quite different for tree species, which were all more depleted in ¹³C than the tree-leaf bulk δ¹³C values (from ?27‰ to ?32‰). Formaldehyde in ambient air at the forest site had δ¹³C values different from those of leaf-emitted formaldehyde, indicating other sources for ambient formaldehyde apart from direct emission from leaves, most probably the photooxidation of biogenic hydrocarbon like isoprene and monoterpene. The δ¹³C differences of acetaldehyde between ambient data and those of tree leaves emission were less than 1‰, implying direct biogenic emission as the dominant source.     

Copper ultrastructural localization, subcellular distribution, and phytotoxicity in Hydrilla verticillata (L.f.) Royle

Laboratory experiments were conducted to investigate copper (Cu) subcellular distribution and toxicity in Hydrilla verticillata. Fronds were subjected to different concentrations (15, 75, and 150 μM) of Cu for 7 days. Cu grains were found in cell walls, plasmodesmata, and within the nuclei and chloroplasts using the autometallographic technique. Subcellular fractionation of Cu-containing tissues indicated that in leaves subjected to high Cu concentrations, 59–65 % of the element was located in the cell wall fraction, followed by cell organelles (21–30 %) and the soluble fraction (10–14 %). The levels of K, P, Zn, and Mg declined under all Cu concentrations, but Ca, Mn, and Fe contents reached their peak at 15 μM Cu and decreased thereafter. F _v/F _m, F ₀, and F _m fell significantly in line with the decrease in pigment content. Cu exposure also caused significant damage to the chloroplasts, mitochondria, and nuclei, including disintegration of the chloroplasts and vacuolization of the mitochondria and nuclei, all of which suggested that Cu hastened plant senescence. The Cu maximum permissible concentration for H. verticillata was 10 μM, which was less than the existing general water quality standard. This suggested that H. verticillata could be used to assess Cu phytotoxicity.     

镍的作物效应及临界值研究

在三种紫色土（酸性，中性，石灰性）上添加Ｎｉ（０，１０，３０，６０，１００，２００ｍｇ／ｋｇ土）进行莴笋盆栽试验，结果表明：低浓度的Ｎｉ能刺激作物生长，而高浓度的Ｎｉ则阻碍作物生长，使叶片黄化。三种土因性质及本身肥力水平的差异，使酸性紫色土上作物Ｎｉ最敏感，石灰性紫色土上次之，中性紫色土上最不敏感，且Ｎｉ在作物体内分配规律也有所不同，比较了土壤全Ｎｉ，有效Ｎｉ，植株根Ｎｉ作为的临界值的优越性，结果     

中国生态农业与绿色食品

本文从农业环境问题和食品安全性出发，阐述了中国生态农业的兴起及特点，绿色食品生产的要求，生态农业与绿色食品的关系。介绍了几种可用于开发绿色食品的优化生态模式。