构造煤中煤层气扩散-渗流特征及其机理

煤层气产出一般要经过解吸、扩散和渗流三个阶段,而煤层气在变形较强的构造煤中的扩散过程不同于在原生结构煤或变形较弱的煤体中的扩散。外界压力的变化只是构造煤吸附与解吸整个过程的一种外在因素,构造煤的变形和结构变化以及吸附势场的转换才是构造煤吸附与解吸的内在因素,是导致解吸过程不可逆性的根本原因。当构造煤体与CH4等多元气体间的吸附平衡状态遭到破坏时,变形较强的构造煤在降压后会产生解吸滞后现象;而变形较弱的煤,分子结构中的气体会很快解吸,第一阶段是气体解吸作用,第二阶段是游离气体从微孔向较大孔隙扩散的过程,气体扩散速率主要由第二阶段决定。构造煤气体扩散机理主要是由孔隙形状、大小、连通性和多元气体性质和状态所决定的。韧性变形煤的微孔隙比较发达,所以韧性变形煤以Knudsen扩散为主,脆性变形煤的中、大孔隙所占比例较大,而且脆性变形煤的孔隙之间具有很好的连通性,所以脆性变形煤以Fick型扩散为主,脆-韧性变形煤以及接近脆-韧性变形煤的脆性变形煤和韧性变形煤均以过渡型扩散为主。在试井渗透率比较中,一定变形程度的脆性变形煤>韧性变形煤,脆性变形煤中以过渡孔为主,其余为微孔,测不出亚微孔和极微孔,脆性变形还增加了各孔隙之间的相互连通性。韧性变形煤中过渡孔比表面积所占比例下降,微孔和亚微孔增高,扩散主要发生在微孔和过渡孔中,所以韧性变形煤的试井渗透率低于脆性变形煤的试井渗透率。     

土壤对氟离子吸附与解吸的动态土柱法研究

用饱水动态土柱法对氟离子的吸附与解吸特征及其反应动力学特征进行了初步探讨。结果表明，氟离子的吸附与解吸特征可分别用Ｌａｎｇｍｉｕｒ模型和Ｆｒｅｎｄｌｉｃｈ模型来表征。而氟的吸附与解吸反应动力学均可用Ｅｌｏｖｉｃｈ方程来描述。吸附与解吸过程是一个由反应速率控制的不可逆过程。     

藻吸附金属离子的研究—斜生栅藻富集金

发展了一种新的金属离子的分离富集方法－微生物吸附法，重点研究了斜生栅藻对的吸附和解吸条件，其吸附率和解吸回收率均大于９５％，首次用藻类分离富集了地质样品中的痕量Ａｕ，其标准加入回收率大于９１％，用原子吸收法测定标样中痕量金，其结果与推荐值相符，此外，机理探说明：斜生栅藻富集金的过程起主要作用的是络合吸附，随吸附时间的增长也发生生物吸收作用，同时，伴有氧化还原反应发生。     

混合菌种对地下水中三氯乙烯的生物降解和吸附解吸的实验研究

由于氯代有机溶剂的大量使用和不合理的处置 ,致使三氯乙烯 (以下简称TCE)成为地下水中常见的有机污染物。本实验以TCE为靶污染物 ,采用批试验方法 ,研究了灭菌后的混合菌种对不同浓度TCE的吸附影响。实验结果表明 :当TCE浓度在 10～ 2 0 0mg l范围内 ,TCE的吸附模式符合Cs =0 17976C2 36 39e 等温方程 ;TCE的解吸模式符合C =0 0 2 987C2 1 46 1 e 等温方程 ;吸附在 15min内平衡 ;解吸在 1h内平衡。     

临安和上甸子大气本底站大气中NMHCs组成与浓度的变化特征

为研究中国大气中非甲烷烃(NMHCs)区域性本底浓度与变化特征,采用吸附富集—热脱附—气相色谱法,测定了临安(30°25′N,119°44′E,海拔132.0 m)和上甸子(40°19′N,117°07′E,海拔286.5 m)大气本底站大气中NMHCs的组成与浓度。从2003年10月至2004年7月,先后按季度分4次观测与取样,共获145个有效样品。检测出C2-C10的NMHCs组分52个,其中包括26个烷烃、17个烯烃和9个芳香烃化合物。在临安和上甸子大气中非甲烷烃总烃(TNMHCs)的平均质量浓度分别为(238.5±126.0)×10-9C,(278.7±185.5)×10-9C。两站烷、烯、芳香烃在TNMHCs中所占的比例相近,分别约为21%—33%,7%—19%,54%—70%。受源、汇和气象条件的共同影响,NMHCs浓度存在明显地日变化和季节性变化,但变化趋势两地略有不同。TNMHCs平均浓度的峰值都出现在10月,谷值分别出现在1,7月。气象要素以风向和风速的影响最为明显。TNMHCs高浓度大多与上风向存在较强污染源有关。另外发现,临安TNMHCs浓度比10 a前有明显增加。     

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.     

Sequestration of organic contaminants in soil/sediment and its impact on contaminant fate

Adsorption and desorption are critical processes controlling the fate and transport of organic contaminants in natural environment. Numerous studies have shown that only a fraction of contaminants in soil or sediment can readily be desorbed to the aqueous phase, while desorption of the remaining fraction is very difficult and does not follow the conventional desorption models-a phenomenon typically referred to as ＂resistant desorption＂ or ＂sequestration＂ and is argued by many as the cause of reduced availability of contaminants in soil and sediment. While this reduced availability often reduces the effectiveness of soil and sediment remediation, the same effect can also greatly reduce risk of contaminated soil and sediment. The authors have conducted extensive lab and field studies to characterize the unique properties of sequestration of organic contaminants and to understand the mechanism（s） controlling sequestration. Thus far, over 50 different contaminant-soil/sediment combinations have been evaluated, using contaminants of varied physical-chemical properties （e.g., chlorinated benzenes, PAHs, PCBs, DDT, atrazine, hexachlorocyclohexane isomers, etc.）. Several unique characteristics of sequestration have been observed, and the most striking one is that despite the significant differences in chemical and soil properties, desorption of sequestered contaminants for all the contaminant-soil/sediment combinations exhibited very similar KOC （organic-carbon normalized partition coefficient） and very similar desorption kinetics.     

Phosphate sorption desorption characteristics of some ferruginous soils of tropical region in Eastern India

Phosphate sorption and desorption experiments were conducted with four ferruginous soils (alfisols) of Eastern India, in view of the low native phosphate concentrations in tropical Indian soils. From the P-isotherm curve, standard P requirement (SPR) of the soils was determined. Phosphate sorption data were fitted to both Langmuir and Freundlich equations and mean sorption maximum values obtained for the different soil series were in the decreasing order as Matimahal > Anandapur > Mrigindih > Kashipur. The fraction of added P sorbed followed the same trend as SPR, P sorption maximum (P_max), phosphate affinity constant (K), maximum phosphate buffering capacity (MPBC), Freundlich constant K′ and phosphate desorption values. Phosphate sorption maximum was significantly correlated with MPBC, Freundlich 1/n, SPR, clay and different forms of Fe and Al. The value of K (bonding energy) was significantly correlated with MPBC, Freundlich K′ and pyrophosphate extractable Fe and Al. The MPBC was significantly correlated with Freundlich K′, Freundlich constant 1/n, clay, oxalate and dithionite extractable, amorphous and crystalline form of Fe and Al. Freundlich K′ was significantly correlated with Freundlich 1/n, pH_water, clay, dithionite extractable and crystalline form of Fe and Al. The results suggested that the soils having higher amount of extractable and reactive Fe and Al shared higher P sorbtion capacity and such soils may need higher levels of P application     

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.     

介绍一种简易快捷的煤层瓦斯含量的计算方法

大量煤层瓦斯解吸资料表明，解吸瓦斯量（Q）与煤样气体解吸时间的开方（θ），呈Q=ab/θ（b＜0）曲线的相关关系一依据这种关系，由现场瓦斯煤样的解吸资料，建立起θ与Q的回归方程，再按《煤层气测定方法（解吸）MT／T77—1994》中的有关规定计算出损失瓦斯及在化验室测试的常温下煤层瓦斯的自然组分、可燃物质量等数据，进而便可求得煤层瓦斯含量值。该方法在江西省丰城矿区石上井田勘探工作中取得了较好的效果。