水溶液中腐殖酸和苯酚在ZH-02树脂上的双组分吸附

通过苯甲酰基修饰的苯乙烯-二乙烯苯吸附树脂ZH-02对水中腐殖酸和苯酚进行了单组分和双组分的静态吸附.结果表明,在腐殖酸为主要吸附质的二元组分溶液中,对苯酚的吸附量的影响可以利用IAST模型进行预测;而在不存在主要吸附质的二元溶液中,可以用单组分体系的平衡吸附量近似预算双组分竞争体系时各组分的平衡吸附量.     

Temporal and spatial relationships in fine particle strong acidity, sulphate, PM1O, and PM2.5 across multiple canadian locations

The Canadian Acid Aerosol Measurement Program (CAAMP) was established in 1992 to gain a better understanding of the atmospheric behaviour of fine particle strong acidity (“acid aerosols”) and to facilitate an assessment of the potential health risks associated with acid aerosols and particles in general. During 1992. 1993 and 1994, annular denuder and filter measurements were taken at four sites in Ontario, two in Quebec, three in the Atlantic Provinces and one in the greater Vancouver area. Mean fine particle sulphate concentrations (SO₄²⁻) were highest in southern Ontario (annual average ranged from 40–70 nmol m⁻³), lowest at a site in the Vancouver area (average = 16 nmol m⁻³) and second lowest in rural Nova Scotia. However, mean fine particle strong acid concentrations (H⁺) were geographically different. The highest mean concentrations were at the east coast sites (annual average of up to 30 nmol m⁻³). Acidities were lower in areas where the fine particle acidity experienced greater neutralization from reaction with ammonia. This included the major urban centres (i.e. Toronto and Montréal) and areas with greater amounts of agricultural activity, as in rural southern Ontario. On average, ambient concentrations of fine and coarse particle mass were larger in the urban areas and also in areas where SO₄²⁻ levels were higher. All the particle components were episodic. However, compared to SO₄²⁻ and fine particles (PM_2.5 or PM_2.1, depending upon inlet design), episodes of H⁺ tended to be less frequent and of shorter duration, particularly in Ontario. Saint John, New Brunswick, had the highest mean annual H⁺ concentration, which was 30 nmol m⁻³. H⁺ episodes (24 h concentration > 100 nmol m⁻³) were also the most frequent at this location. The high levels in Saint John were partially due to local sulphur dioxide sources and heterogeneous chemistry occurring in fog, which, on average, led to a 50% enhancement in sulphate, relative to upwind conditions.There was a substantial amount of intersite correlation in the day to day variations in H⁺, SO₄²⁻ , PM_2.5 and PM₁₀ (fine + coarse particles) concentrations, which is due to the influence of synoptic-scale meteorology and the relatively long atmospheric lifetime of fine particles. Sulphate was the most regionally homogenous species. Pearson correlation coefficients comparing SO₄²⁻ between sites ranged from 0.6 to 0.9, depending on site separation and lag time. In many cases, particle episodes were observed to move across the entire eastern portion of Canada with about a two-day lag between the SO₄²⁻ levels in southern Ontario and in southern Nova Scotia.     

南京市“十五”期间环境空气质量状况解析

综述并分析了南京市“十五”期间环境空气质量状况,指出空气中首要污染物仍为可吸入颗粒物.南京市虽然主要工业污染物排放总量继续得到有效控制,部分污染物明显缩减,空气质量有所改善,但酸雨污染依然严重,控制和治理二氧化硫污染已刻不容缓,要采取合理科学规划,加大工业污染治理力度,同时要增强市民自我环境保护意识.     

Synchronous-scan fluorescence spectra of Chlorella vulgaris solution

The characterization of the Chlorella vulgaris solution was carried out using synchronous-scan spectroscopy. The range of concentration of algae and Fe(III) in aqueous solutions were 5 × 10⁸–8 × 10⁹ cells l⁻¹ and 10–60 μM, respectively. Effective characterization method used was synchronous-scan fluorescence spectroscopy. The wavelength difference (Δλ) of 90 nm was maintained between excitation and emission wavelengths; 90 nm was found to be the best Δλ for effective characterization of Chlorella vulgaris solution with or without quencher species (e.g., Fe(III), humic acid (HA)) for the first time. The peak was observed at about EX 236.6 nm/EM 326.6 nm for synchronous-scan fluorescence spectra. The fluorescence quenching of algae in system of algae–Fe(III)–HA was studied using synchronous-scan spectroscopy for the first time. Fe(III) was clearly the effective quencher. The relationship between I₀/I (quenching efficiency) and c (concentration of Fe(III) added) was a linear correlation for the algae solution with Fe(III). Also, Aldrich humic acid was found to be an effective quencher. pH effect on synchronous-scan fluorescence intensity of algal solution with Fe(III) and/or HA was evident.     

涤纶碱减量废水中对苯二甲酸的好氧生物降解性能研究

采用城市污水处理厂的活性污泥做菌源,在实验室条件下研究了对苯二甲酸(TA)和乙二醇(EG)的好氧生物降解性能,着重考察了EG对TA好氧生物降解性能的影响.试验结果表明,微生物以TA、EG作为惟一的碳源需要一定的驯化时间,EG作为惟一碳源的驯化时间比TA的驯化时间长.但微生物一旦被驯化,EG比TA具有较快的降解速度,当TA为1100mg/L时,其平均降解速率为27.5 mg COD/g MLSS·h,而EG为1200mg/L时,其平均降解速率达到36.7 mg COD/g MLSS·h.在相同污泥负荷条件下,TA降解的滞后期受TA浓度影响不大,TA的好氧降解不存在明显的抑制浓度.EG不会抑制TA的初级生物降解,但会抑制TA的最终生物降解.     

臭氧-曝气生物滤池处理酸性玫瑰红染料废水

在实验室配制含酸性玫瑰红染料的印染废水,采用臭氧氧化-曝气生物滤池工艺开展处理试验.试验运行结果表明,臭氧氧化处理能提高模拟废水的可生化性,BOD/COD值由原水的0.18上升到0.36.经组合工艺处理后出水COD＜40 mg/L,色度40倍以下,SS约50 mg/L,处理效果良好.     

脱硫石膏农业利用研究进展与展望

概述火电厂脱硫石膏定义、生产过程和性质.简述了脱离石膏的工业利用,详述了脱离石膏对酸性和碱性土壤改良的现状和机理,并展望了脱硫石膏促进滩涂土植被演替的前景.     

空气与废气中的正丁烷、丁酮、醋酸异丙酯的快速测定法

采用活性炭吸附，二硫化碳解析，毛细管气相色谱法同时测定空气与废气中的正丁烷、丁酮、醋酸异丙酯，采样体积以45L计，方法最低检出限分别为：正丁烷0．002mg／m^3，丁酮0.0024mg／m^3，醋酸异丙酯0．0028mg／m^3。     

微波解吸柠檬酸盐溶液中SO2实验研究

结合微波具有的热效应、非热效应特性，利用经改装的微波反应装置，研究了微波场下柠檬酸浓度、微波作用时间、微波功率、SO2初始浓度和搅拌速率对解吸柠檬酸盐溶液中SO2的影响，得出了影响SO2解吸率的基本规律和最佳解吸条件，并进行了分析。     

Characteristics of MnO2 catalytic ozonation of sulfosalicylic acid and propionic acid in water

The characteristics of different types of MnO₂ catalytic ozonation of sulfosalicylic acid (SSal) and propionic acid (PPA) have been investigated in this paper. The experimental results show the dependence of catalytic activity of MnO₂ on organic compounds and the pH of solutions, but it is independent on the type of MnO₂. For example, three types of MnO₂ have not any catalytic activity when ozonation of PPA under the condition of this experiment. All MnO₂ catalytic ozonation of SSal at pH=1.0 have a greater total organic carbon removal than ozonation alone has, however, at pH=6.8 and 8.5, catalytic efficiency is not observed. Furthermore, the batch experimental results indicate that there are no direct relationship between the activity of metal oxide catalytic decomposition of ozone and that of its catalytic degradation of organic compounds.