洗毛废水和煮茧废水处理技术探讨

本文主要介绍洗毛废水和煮茧废水的盐析和生化特点，结合制定了物化－接触氧化处理工艺。     

三氯甲烷对土壤酶活性影响

通过实验室内培养,研究了三氯甲烷(CF)在7种不同的浓度下对土壤过氧化氢酶、蛋白酶活性所产生的影响.结果表明:在实验时间内,CF对蛋白酶活性起到抑制作用,对过氧化氢酶活性则表现出激活效应.质量分数大于60.00 mg·kg-1的CF会明显抑制蛋白酶活性;CF对这2种土壤酶的作用强度大小的浓度有关.浓度小时作用强度小,浓度大时作用强度大;CF[ω(CF)≤60.00 mg·kg-1]对这2种土壤酶的作用是暂时的,过一段时间后会恢复,即对这2种土壤酶的作用有抑制(激活)-恢复过程,恢复程度和质量分数有关,质量分数越大恢复程度越小.     

磷石膏中杂质的形态及水溶性磷对水泥物理性能的影响

在对磷石膏中杂质的类型、存在形式及磷石膏的溶解性质检测分析的基础上 ,研究了磷石膏中水溶性磷含量以及磷石膏直接替代天然石膏用作水泥缓凝剂对水泥质量的影响。结果表明 ,磷石膏中的主要杂质为 :以H3PO4、H2 PO-4 或HPO2 -4 形式存在的可溶性P2 O5、与金属共生磷酸盐复合物和共晶形式存在的不溶性P2 O5及石英。磷石膏中的水溶性磷含量 <1%时 ,对水泥物理性能的影响不大 ,磷石膏中的水溶性磷含量 >1%时 ,水泥的凝结时间明显延长 ,但对强度影响不大     

健美操课对我校女生体质健康的影响

通过几年来将健身健美操运动引入高校女生体育课教学中的实践表明,健美操运动能较全面改善女大学生的身体外形结构,消除多余脂肪,增强肌力,提高身体素质,对其形体美、气质美有良好的促进作用。同时能有效的改善心肺功能,提高人体的有氧代谢能力,并能为贯彻终身体育思想打下良好的基础。     

重金属Cd、Zn、Pb复合污染对土壤酶活性的影响

采用回归正交设计方案 ,研究了潮褐土中Cd、Zn、Pb复合污染对 4种土壤酶活性 (过氧化氢酶、脲酶、碱性磷酸酶、转化酶 )的影响 .结果表明 ,在复合效应影响中 ,重金属对土壤酶活性的抑制效应顺次为Cd >Zn >Pb ;同时 ,Cd、Zn、Pb复合污染对 4种土壤酶活性的影响效应存在着明显差异 .其复合污染对脲酶表现出协同抑制负效应的特征 ;对过氧化氢酶表现出一定的屏蔽作用 ;对转化酶和碱性磷酸酶活性影响则主要随着Cd浓度的增加而显著降低 .离子冲量与土壤脲酶活性之间呈显著负相关 ,用脲酶活性作为预测土壤重金属Cd、Zn、Pb复合污染程度的主要生化指标具有一定的可行性     

受污染水体的水质恢复方法

大量未经处理的污水排入水体时 ,会导致地面水体严重污染。受污染水体的水质恢复方法有物理法、化学法和生物法 ,它们能控制水体外源性和内源性污染物的排入量、人工强化水体自身的净化能力 ,以降低水体中污染物的浓度、提高溶解氧浓度 ,恢复水生生物的多样性     

Degradation of para-hydroxybenzoic acid by means of mixed microbial cultures

Olive mill wastewater contains some phenolic compounds that cause antibacterial activity of a kind that prevents biological treatment without previous dilution. Among these phenolic compounds, p-hydroxybenzoic acid (PHB) is considered to be one of the most representative. This work examines the biodegradation of PHB by aerobic microbial mixed cultures previously acclimatized to glucose, which was used as an easily biodegradable model compound. Microbial growth runs were carried out in a batch reactor in the PHB concentration range of 200-1000 mg/L. In all the runs the PHB proved to be completely degradable. The specific growth rates obtained were in the range of 0.16-0.35 l/h. Experimental runs showed that the functional relationship between the specific growth rate and PHB concentration was that proposed by Monod. The kinetic constants of the Monod equation (mu(max) and K(S)) and biomass yield coefficient (Y) were determined experimentally. With the parameter values thus obtained, a mathematical model that also takes account of the duration of the lag phase was employed to describe both the microbial growth and the consumption of PHB. The concentration values of the model fit well with the data obtained experimentally.     

饮用水生物处理中微生物量和活性的测定方法

微生物量和微生物活性是饮用水生物处理工艺设计与运行的重要参数。总结论述了适用于表示饮用水生物处理过程生物膜中微生物数量和活性的几种主要指标的测定方法。     

滇池底泥微生物菌群对微囊藻毒素的生物降解

采用滇池水华蓝藻中提取提纯的微囊藻毒素(microcystins,MCs)作为微生物生长的碳源和氮源,从长期暴露于蓝藻水华的滇池底泥中,通过从含低浓度到高浓度MCs的逐步培养驯化,获得了高效降解MCs的微生物混合菌群,在初始MC-RR和LR浓度大约分别为50 mg/L和30 mg/L下,3 d内可将MCs全部降解.进一步活性研究显示,不同含碳和含氮化合物虽然能够促进混合微生物菌群的生长,但对降解MCs却无明显的促进作用,说明MCs既可以作为微生物生长的碳源,又可以作为微生物生长的氮源,在富含有机物的天然水体中并不一定能够促进微生物对MCs的生物降解.     

Kinetics of OH-initiated oxidation of oxygenated organic compounds in the aqueous phase: new rate constants, structure–activity relationships and atmospheric implications

The kinetics of OH oxidation of several organic compounds of atmospheric relevance were measured in the aqueous phase. Relative kinetics were performed using various organic references and OH sources. After validation of the protocol, temperature-dependent rate constants for the reactions of OH radical with ethyl ter-butyl ether (, E_a/R=580 (±560) K), n-butyl acetate ( (±0.4)×10⁹ M⁻¹ s⁻¹, E_a/R=1000 (±200) K), acetone ( (±0.05)×10⁹ M⁻¹ s⁻¹, E_a/R=1400 (±500) K), methyl ethyl ketone (, E_a/R=1200 (±200) K), methyl iso-butyl ketone (, E_a/R=1200 (±300) K) and methylglyoxal (, E_a/R=1100 (±300) K) were determined. A non-Arrhenius behavior was found for phenol, in good agreement with the contribution of an OH addition to the mechanism, which also includes H-abstraction by OH radicals. Global rate constants of acetaldehyde, propionaldehyde, butyraldehyde and valeraldehyde were studied at 298 K only, as these compounds partly hydrate in the aqueous phase. All the obtained data (except those of phenol) complemented by literature data were used to investigate three methods to estimate rate constants for H-abstraction reactions of OH radicals in aqueous solutions when measured data were not available: Evans-Polanyi-type correlations, comparisons with gas-phase data, structure activity relationships (SAR). The results show that the SAR method is promising; however, the data set is currently too small to extend this method to temperatures other than 298 K. The atmospheric impact of aqueous phase OH oxidation of water-soluble organic compounds is discussed with the determination of their global atmospheric lifetimes, taking into account both gas- and aqueous-phase reactivities. The results show that atmospheric droplets can act as powerful photoreactors to eliminate soluble organic compounds from the atmosphere.