滇池泥炭土对两种抗生素和双酚A的吸附

用不同浓度NaOH溶液处理采集自云南滇池的泥炭土,研究处理前后的泥炭土对两种抗生素磺胺甲恶唑（SMX）、卡马西平（CBZ）及双酚A（BPA）的吸附机理,并深入探讨3种污染物及泥炭土性质对吸附特性的影响.吸附等温线拟合结果表明,Freundlich模型对3种物质在泥炭土上的吸附等温线有较好的拟合优度.3种物质中,BPA的非线性指数n值最低,这可能是由于其不对称的结构特征导致.随着处理泥炭土的NaOH浓度增加,3种吸附质在泥炭土上的吸附顺序为BPA > CBZ > SMX,BPA的吸附最高可能是由于其含有两个酚羟基,与泥炭土有较强的极性作用导致,而CBZ的吸附比SMX的吸附高是由憎水性作用引起.NaOH处理后并没有增加泥炭土对这3种吸附质的吸附,说明对于离子型化合物,吸附过程和机理复杂,BPA蝴蝶状结构及苯环上含有两个羟基可能导致其在泥炭土上出现特异性吸附,这导致其吸附系数最高;NaOH处理后泥炭土的有机碳含量增加但比表面积可能降低,从而使3种污染物的吸附降低.因此,本研究3种离子型化合物在泥炭土上的吸附受到吸附质的官能团及溶解度、泥炭土的有机碳含量及官能团等多种因素的影响.     

重庆西部山区典型湖泊水-气界面CO2交换通量及其影响因素

为了解我国西南山区湖泊水体CO_2的释放/吸收特征,于2017年7月对重庆西部山区典型9个湖泊表层水体溶解性无机碳进行调查,并同步监测关键环境因子,运用薄边界层法和静态箱法对其水-气界面CO_2通量[F(CO_2)]进行比较研究.结果表明,渝西山区湖泊夏季表层水p(CO_2)介于2.1~45.0 Pa之间,均值为(18.1±12.1) Pa;模型法和静态箱法计算的CO_2通量均值分别为(-8.0±2.9)、(-3.4±3.6)和(-7.1±22.3) mmol·(m2·d)-1,总体表现出大气CO_2汇的特征.水体p(CO_2)和F(CO_2)与关键环境因子的相关分析,表明表层水p(CO_2)和F(CO_2)与风速和ORP显著正相关,与pH显著负相关.     

Tuning of activated sludge in winter based on respirogram profiles under standard and site temperatures

Respirograms of activated sludge OUR_ x~Tand OUR_x~(20)were measured under site(T) and standard(20°C) temperatures, respectively, and the predicted standard temperature respirogram OUR_( x,cal)~(20)was also calculated using the Arrhenius equation. These respirogram profiles reveal more information than effluent quality. A decrease of OUR_ x ~(20)is a critical alarm signal for the loss of pollutant removal capacity, and a sudden increase of the predicted value OUR_( x,cal)~(20)is an alarm signal for the unrecoverable deterioration of biomass. The sign of OUR_x~(20)–OUR_(x,cal)~(20)can be used for selection of tuning strategies. For example, a negative value of OUR_x~(20)–OUR_( x,cal)~(20)indicates that doubling biomass is difficult,thus strategies such as extending the reaction time with limited available biomass is preferred. The findings in this study elucidated the respiration profile of activated sludge under changes of temperature and can be effectively used for the stable operation of Wastewater Treatment Plants under cold temperatures and seasonal variations.     

原子捕集——火焰原子吸收光谱法测定环境土壤中痕量镉

系统地考察了原子捕集测定环境土壤中镉的条件及10余种常见共存离子的干扰情况，测定环境土壤中镉含量原子捕集灵敏度较常规原子吸收光谱法高112倍，可达0.25μg/L/1%A，方法快速、简便、稳定，令人满意。     

基于生物光学模型的晋江悬浮物遥感估算

为了建立以生物光学模型为基础的河流悬浮物遥感估算方法,以福建晋江为例,对福建晋江下游河段的光学特性和悬浮物浓度进行了测定,探讨了水面下反射率R(O-)与悬浮物浓度之间的响应关系.结果表明,绿光波长的反射率与悬浮物浓度的相关性最强,因此,用R(O-)TM2与悬浮物浓度建立了遥感估算模型,并将其应用于2008年2月28日的Landsat TM影像,反演出晋江的悬浮物浓度分布.精度分析说明,平均相对误差RE为11.93%,该模型可以有效地应用于Landsat TM反演悬浮物浓度.     

影响悬浮颗粒物吸收系数测量的相关因素研究

水体悬浮颗粒物吸收系数是水色遥感研究中的关键参数之一,为研究不同因素对吸收系数测量结果的影响,分别采用透射法(T法)、透射反射法(T-R法)和吸收法(A法)测量颗粒物吸收系数.结果表明,A法在测量悬浮颗粒物吸收系数时受滤膜差异性、滤膜含水量以及滤膜颗粒物分布不均匀等因素的影响较小,测量精度较高.对不同测量方法的光程放大因子的研究结果表明,不同测量方法,不同颗粒物富集量会有不同的光程放大因子.采用线性拟合的方法求得A法、T法和T-R法的平均光程放大因子为4.01、2.32和2.20,相关系数分别为0.90、0.80和0.87.对于A法和T-R法,采用二次多项式拟合的方法计算光程放大因子可以提高测量精度,相关系数分别为0.95和0.94.对比各影响因素对测量结果造成的平均相对误差发现,光程放大因子是颗粒物吸收系数测量最大的误差来源.     

国标与FCC美标手机比吸收率研究

针对国标与FCC美标在标准限值和测试部位的差异,通过实际测试采集数据对标准之间差异部分进行比对研究。     

Chlorfenvinphos Dermal Absorption in Rats: Histological and Ultrastructural Changes in the Skin and Internal Organs

We studied the effect of chlorfenvinphos dermal absorption on the morphological picture of blood, on the histological and fine structure of tail skin, and on the histological structure of internal organs (lungs, heart, liver, spleen, and kidney) of rats. This study was conducted on 25 white Wistar rats, the tail skin of which was—or was not—hydrated before exposure. Rat tails were soaked in 0.5% or 0.05% chlorfenvinphos for 1 hr day for 3 months. Evident tendencies for a decrease in the absolute level of leukocytes and for an increase in the absolute level of erythrocytes in all experimental animals were observed. Histopathological changes in the internal organs were mildly manifested in only a few rats, mainly as liver and pulmonary hyperaemia. Rat tail skin at the direct exposure site showed hyperceratosis, intensive desquamation, and compensatory hyperplasia.     

混合有机胺吸收烟道气中CO2的实验研究

以工业应用为背景,采用双搅拌釜反应器,对DETA(二乙烯三胺) MDEA(N-甲基二乙醇胺)、TETA(三乙烯四胺） MDEA混和有机胺水溶液吸收模拟烟道气中CO2进行研究。结果显示,在MDEA中加入少量烯胺DETA、TETA,可显著提高CO2吸收速率和吸收容量,增强传质效果。其吸收CO2的效果优于常用的MEA(-乙醇胺)和DEA(二乙醇胺)。     

Lead removal from contaminated water using mineral adsorbents

This study records experiments undertaken to determine the suitable conditions for the use of naturally occurring minerals (talc, chalcopyrite and barite) as an adsorbent for the removal of lead ions from liquid wastes. The adsorption of lead ions from solutions containing different initial lead concentrations (50, 100, 200, 400, 600, 800 and 1000 mg l^–1 Pb as lead nitrate) using different size fractions (<63 m, 63–150 m) of talc, chalcopyrite and barite at different pH (3, 5, 7 and 9) and different adsorption times (24, 48, 72 and 96 hr) was examined. The results revealed that of the studied minerals, the chalcopyrite fraction at 63–150 m showed the highest adsorption capacity. The adsorption data of Pb ions was also analyzed with the help of the Langmuir and Freundlich models to evaluate the mechanistic parameters associated with the adsorption process. The adsorption isotherms obtained from the Langmuir and Freundlich equations were generally linear and the adsorption of Pb by the studied minerals was correlated with the adsorption maximum and binding energy constant of the Langmuir equation and equilibrium partition constant and binding partition coefficient of the Freundlich equation. It was concluded that the equilibrium time of adsorption was 72 hr at an optimum pH from 7 to 9. This technique might be successfully used for the removal of lead ions from liquid industrial wastes and wastewater.