上覆水溶解氧水平对苏州城市河道底泥吸附/释放磷影响的研究

为了解上覆水体中溶解氧水平对底泥释放磷的影响,采用室内静态模拟的方法,控制在无外源污染的情况下,模拟水体的三种溶解氧水平范围,好氧、厌氧和自然状况,研究不同的溶解氧水平对底泥释放或吸附营养盐的影响。研究结果表明,溶解氧小于0.5mg/L的厌氧状况能加速底泥中磷的释放,溶解氧大于5.0mg/L的好氧状况则抑制底泥中磷的释放。因此要提高水质,降低内源负荷(底泥中)磷的释放,应该控制水体中的各种耗氧物,提高水体的溶解氧水平。     

水体富营养化状态对城市河道底泥吸附/释放P的影响——以江苏省苏州市河道试验研究为例

以苏州古城区内的河道为研究对象,采用静态培养的方式,研究了上覆水体不同富营养化程度对底泥中P释放/吸附的影响。研究结果表明：截断外源污染后,苏州河道底泥对水体中营养盐P呈现吸收状态;随着上覆水体磷酸盐浓度的增大,单位面积底泥累积吸收的磷酸盐就越多;上覆水与底泥比值越大,底泥对P的吸附率有减小的趋势。     

水体富营养化状态对城市河道底泥吸附/释放P的影响 ——以江苏省苏州市河道试验研究为例

以苏州古城区内的河道为研究对象,采用静态培养的方式,研究了上覆水体不同富营养化程度对底泥中P释放/吸附的影响。研究结果表明：截断外源污染后,苏州河道底泥对水体中营养盐P呈现吸收状态;随着上覆水体磷酸盐浓度的增大,单位面积底泥累积吸收的磷酸盐就越多;上覆水与底泥比值越大,底泥对P的吸附率有减小的趋势。     

城市重污染河道环境因子对底质氮释放影响

以苏州市古城区劣Ⅴ类水体为研究对象,利用模拟试验方法,研究和探讨了水体环境条件(DO、Eh、pH值、温度)变化和疏浚深度对河道底泥氮释放的影响.底泥供试样中NH₄+-N与NO₃--N含量一般为0.277 g/kg与0.0012g/kg,上覆水体NH₄+-N与NO₃--N含量一般为6.743 mg/L与1.500 mg/L.试验结果表明:厌氧环境(DO<0.5 mg/L)、强还原环境(Eh<-108 mV)、酸性环境(pH<6.0)及温度升高均有利于底泥中NH₄+-N的释放,NO₃--N的迁移转化规律则相反;供试样控制疏浚深度5 cm、10 cm、15 cm、20 cm,当疏浚深度15 cm时,泥-水界面向上覆水体中扩散的氮通量最小;疏浚深度、DO和Eh对底泥NH₄+-N释放程度的影响大于pH和温度,通过曝气等方式保持水体中适当的溶解氧或使底泥保持较强的氧化电位环境可以有效抑制底泥中NH₄+-N的释放.     

鉴江河口底泥盐度释放规律研究

底泥盐度释放是河口水资源利用的主要限制因子。本文以鉴江为例,基于野外实测与室内实验,系统分析了鉴江河口底泥盐度及水体氯离子的分布特征;通过振荡、换水及静态等实验。定量研究了河口底泥盐度释放规律。结果表明：（1）潮泛河口底泥盐度主要受上溯潮水的影响。有较为明显的梯度性;（2）底泥盐度释放量在初期较大,随着换水周期的累加,则逐步降低;在同一换水周期。底泥盐度释放强度与其本底盐度浓度成正指数关系;（3）静态释放时间越长,上覆水盐度越大。静置30d。三组样品上覆水的浓度分别达2626mg&#183;L-1、932mg&#183;L-1、533mg&#183;L-1。远远超过用水水质的要求。     

水体富营养化与水体沉积物释放营养盐

水体富营养化已经成为世界水环境面临的最为重要的问题.简要介绍了中国水体富营养化的现状和水体富营养化的成因.着重阐述了在截断外源污染后,水体沉积物对营养盐的释放及其主要影响因素,并提出了目前存在的问题和未来的发展方向,为水体富营养化的研究、预防和治理工作提供了系统、科学的理论依据.     

赤砂沸石对氮磷钾吸附与释放的研究

本文以安徽省繁昌县赤砂沸石为试验材料，以黄红壤为参照，研究了丝光沸石为主的天然沸石对ＮＨ、Ｈ＿２ＰＯ及Ｋ￣＋的吸附与释放，结果表明：赤砂沸石的吸铵量和吸磷量为黄红壤的３倍；其中易释放铵和可释放铵占总吸铵量８０％以上；易释放磷和可释放磷占７０％以上；赤砂沸石的速效钾含量为黄红壤的７倍左右，而钾位缓冲容量（ＰＢＣ￣Ｋ）则为黄红壤的３５倍左右。赤砂沸石用做肥料调理剂和土壤改良剂，将能够减少土壤中氮、磷、钾的流失，并提高肥料中养分的利用率。     

土壤对氟离子的吸附和释放实验研究

实验研究了土壤中的粘土矿物对氟离子有良好的交换吸附作用,用饱水动态土柱法对氟离子进行交换吸附处理可使含氟1.6mg/l的饮用水降到0.2mg/l,并且水的各项指标均达到国家饮用水标准,是降氟的很好材料,在水环境治理中发挥了很大作用.     

Mutual effects of fluoride and phosphate on their adsorption and desorption in fluoride-contaminated softs

Phosphate is one of the important nutrients for plant growth. In acidic and highly weathered soils, phosphate is ready to adsorb on Al and Fe oxides and transform into sparsely soluble Fe-P and Al-P solid phases, greatly reducing phosphate bioavailability. Aluminum and iron oxides in soils are important sinks for both phosphate and fluoride. In acidic soils, fluoride adsorption can dramatically facilitate dissolution of Al- and Fe-containing phases, which may influence the distribution and migration of both pollutants and nutrients including phosphate. To date, little information is available on mutual effects of fluoride and phosphate in fluoride-contaminated acidic soils. The objective of this study is to evaluate mutual effects of fluoride and phosphate on their adsorption/desorption in red soil, collected fi＇om Yingtan, Jiangxi Province, China, using a batch equilibrium method. The following results and conclusions were obtained. In heavily fluoride-contaminated soils, the adsorption of both fluoride and phosphate decreases with an increase in solution pH. Phosphate adsorption decreases progressively with increasing concentration of fluoride, suggesting that fluoride competes with phosphate for adsorption sites.     

Seasonal variations of adsorption/desorption equilibrium concentrations of P at water-sediment interface in the Meiliang Bay, Taihu Lake, China

Seasonal variations of adsorption/desorption equilibrium were investigated by collecting overlying water and seasonal sediment from the Meiliang Bay, Taihu Lake, China. At the same time, seasonal variations of TP and P fractions＇ concentrations in the initial and end of adsorption experiment were also carried out. In addition, the effects of temperature on the P translocation process were also conducted and discussed. The following conclusions were obtained： The sequence of adsorption/desorption equilibrium concentrations of P at water-sediment interface was spring〈winter〈autumn. In sediment the concentrations of TP decline. Concentration P decreased with temperature.     

Seasonal variations of adsorption/desorption equilibrium concentrations of P at water-sediment interface in different trophic states of Taihu Lake, China

Sediment from three different trophic states （Meiliang Bay, Xukou Bay and Gonghu Bay） in spring, summer, autumn and winter were collected and analyzed in Taihu Lake. At the same time, seasonal variations in adsorption/desorption equilibrium were investigated with corresponding sediments from these three trophic states, including adsorption efficiency, adsorption/desorption equilibrium concentration and equilibrium adsorption quantity. Variations of TP and P fractions＇ concentrations in the initial and end of adsorption experiment were also documented in order to find the most active P fractions. The following conclusions were obtained： （1） Concentrations of total phosphorus （TP） and its fractions in the sediments were coincided with the trophic state of corresponding overlying water, Meiliang Bay〉Gonghu Bay〉Xukou Bay. The Meiliang Bay located in the north of Taihu Lake is in the eutrophic state and belong to alga-type lake; the Xukou Bay located in the northeast of Taihu Lake is relatively clean lake region; the Gonghu Bay is located in the east of Taihu Lake is in the meso-trophic state. Fe-P concentrations in the Meiliang Bay, Gonghu By and Xukou Bay account for 35.1%-70.9%, 19.6%-26.8%, 16.5%-34.3% of TP, Ca-P account for 20.6%-43.7%, 40.7%-45.0%, 23.0%-41.1% and OP accounts for 15.3%-20.2%, 28.4%-37.4%, 23.6%-54.3%, which changes obviously in different seasons. Fe-P is the major fraction in the eutrophic lake region, which is significantly correlated with the TP concentrations. （2） Adsorption and desorption processes in these three lake regions varied with season.     

Competitive adsorption,release and speciation of heavy metals in the Yellow River sediments,China

The competitive adsorption and the release of selected heavy metals and their speciation distribution before and after adsorption in the Yellow River sediments are discussed. The adsorption of metals onto sediments increases with increasing pH value and decreases with increasing ionic strength. The competitive coefficient K _c and the distribution coefficient K _d are obtained to analyze the competitive abilities of selected heavy metals, which are ranked as Pb > Cu >> Zn > Cd. The competition among selected heavy metals becomes more impetuous with increasing ion concentration in water. Speciation analysis was done by an improved analytical procedure involving five steps of sequential extraction. Cu, Pb and Zn were mainly transformed into the carbonate-bound form (50.8–87.7%) in adsorption. Most of (60.7–77.3%) Cd was transformed into the exchangeable form, and the percentage of carbonate-bound Cd was 19.7–30.4%. The release reaction was so quick that the release capacity of selected heavy metals from sediments to aqueous solution reached half of the maximum value only in 30 s. As opposed to adsorption, the release capacities of selected heavy metals were ranked as Cd > Zn >> Cu > Pb. In this study, Cd produces the most severe environmental hazards, because its concentration in the release solution is 85.8 times more than the human health criteria of US EPA.     

无烟煤对甲烷等温吸附解吸特性实验研究

研究空气干燥基无烟煤对甲烷(CH4)的等温吸附/解吸特性,发现其对甲烷的解吸残余率达56%。为了对其进行深入探讨,特设计了原煤样的炭化和活化实验,扩大了原料的比表面积,进而在等温条件下研究了两个改性样品对甲烷的吸附/解吸特性。对比发现,比表面积的增大能显著增加样品对甲烷的吸附总量,但对解吸残余率没有明显的影响。考虑到影响甲烷吸附/解吸的因素,又在等温条件下对主控因素——水分作了平行实验,结果显示,水分对活化样解吸残余率有明显影响。     

Desorption of zinc by kaolin from Suzhou, China

Heavy metals in soils may adversely affect environmental quality. This paper studied the influence of copper concentration, pH, temperature, and the ratio of solid to solution on the desorption of Zn in kaolin from Suzhou, China in a background solution of 0.01M CaC12 by batch extraction experiments. At 0, 5, 50, 100 mg/L Cu concentrations, for each 0.5, increase in pH between about 1.80 and 3.04 percent desorption decreasing by 3.80%, 13.87%, 9.97%, and 7.65%, respectively. The pH 50 （ pH at 50% Zn desorption） was found to follow the sequence of Cu （5mg/L, pH 50=2.60）.     

Experimental research on adsorption/desorption for petroleum pollutants in the soil in Daqing oilfield

The Daqing oilfield is one of the biggest oilfields in the world. It has been exploited for several decades, which brings serious pollution to local natural environment. The crude oil on ground which is produced in the process of oil production contains various organic pollutants. The petroleum pollutants tend to adsorb, desorb, biodegrade and photolyze and so on in the soil, but adsorption/desorption is a pair of extremely important environment geochemistry behavior. In order to master the rule of petroleum pollutants migration and transformation in the soil environment, and provide scientific evidence for the prevent research project on petroleum pollution treatment in the Daqing oilfield, the chemozem was selected as the experimental sample, which is a kind of representative soil in the Daqing oilfield. The factors affecting adsorbent and desorption＇s characteristics were discussed, including pH of the soil, the concentrations of suspended particulates and temperature. The oscillation-equity was used in the experiment. The mechanism and dynamics process of the adsorption/desorption were researched. The results showed that adsorbing of the petroleum pollutants on the chemozem sediment is a kind of physical adsorption phenomenon. The adsorption function comes from the hydrophobic and sticky character of the petroleum its self. The velocity of adsorption and desorption is almost equivalent, both concentrations of water in the soil are close to the balance in two hours, thus they achieve homeostasis in three hours. The process of adsorption of the petroleum pollutants responses to Herry isothermal model, with increasing pH, concentration of suspended particulates and temperature, the quantity of adsorption show a descending trend. However, desorption is a contrary course of adsorption in the experiment. Due to various influenced phenomena reflect that the soil in the Daqing oilfield has factors, the quantity of desorption shows an ascending trend. These strong adsorption ability to petroleum pollutants.     

远红外作用下不同含水率煤体吸附/解吸能量变化规律

煤体对气体进行吸附/解吸过程的本质是气体分子和煤基质表面分子或原子相互作用的过程,而发生相互作用的本质是能量变化,为了深入研究远红外作用下煤层气吸附/解吸过程及能量变化规律,利用自主研制装置进行远红外作用下不同含水率煤样对CO₂的吸附/解吸实验,然后利用远红外热辐射原理所得的吸附/解吸能量公式对实验结果进行计算,得到不同含水率煤体吸附/解吸过程能量变化规律。结果表明：在远红外作用下,解吸率虽然随含水率增大呈下降趋势,但是下降幅度明显减小,远红外作用可以降低水分对煤层气吸附/解吸能力的影响;远红外作用下不同含水率煤体对气体吸附/解吸过程是一个物理变化,从能量角度可以解释该过程,其变化规律与等温吸附/解吸过程相吻合。研究结果丰富了煤层气增产技术理论。     

我国煤储层煤层气解吸特征

通过大量煤层气勘探井试验测试,对我国各时代不同煤级煤在储层温度和常压条件下气体解吸试验结果进行了系统研究,分析了解吸过程中气体析出的变化规律及煤层气解吸参数的变化态势,探讨了我国煤层气解吸特征的变化,为煤层气采收率研究提供理论依据。     

铁锰氧化物/硅藻土复合物的制备及其对磷的吸附性能研究

采用氧化还原共沉淀法制备铁锰氧化物/硅藻土复合物,考察原料配比、反应温度、焙烧温度及溶液pH值、离子强度对该复合物吸附磷性能的影响,同时开展吸附等温线、XRD和IR等分析。结果表明,2. 5 g硅藻土与1. 0 mmol锰、3. 0 mmol二价铁、3. 0 mmol三价铁制备的复合物在20℃、pH值为6时对磷的吸附量为10. 84 mg/g,较硅藻土提高约3. 6倍;沉淀反应温度对复合物吸附性能影响很小,焙烧温度400～500℃有利于复合物对磷的吸附;吸附量随溶液pH值的增大而减小,pH值较低时吸附作用主要是静电吸引和内层络合,pH值较高时减弱的静电吸引和内层络合与有利于吸附的内层络合共吸附综合作用,表现为吸附量减小;吸附等温线符合Langmuir方程,饱和吸附量34～37 mg/g,与D-R方程、R-P方程有较好相关性,平均吸附能9. 9～11. 3 kJ/mol,复合物具有微孔结构,有单层也有多层吸附。