煤岩吸附二氧化碳气体的CT实验研究   总被引：1，自引：0，他引：1  

郝耐  ;毛灵涛  ;魏峰  ;马甲年 《CT理论与应用研究》2014,(3):425-433

利用工业CT技术及应变测量研究不同气压下煤岩的二氧化碳气体吸附性质。研究发现：煤样的应变随吸附时间和气体压力的增加而增加,且在不同方向是不同的,吸附气体导致煤样孔隙率增加;煤样CT图像的灰度均值和灰度标准差随吸附时间和气体压力的增长都表现出增加的趋势。结果表明：吸附二氧化碳导致煤样总体发生膨胀变形,这为吸附提供更多的孔隙表面积而使吸附气体量增加,含气煤样的密度也因此而增大;气体吸附导致的煤样密度均值增加的效应大于体积膨胀导致的煤样密度均值减小的效应;吸附使煤样内部物质分布不均匀程度增加。  相似文献   

粘土矿物的掺杂对沉积物吸持Cu、Zn能力的影响   总被引：3，自引：0，他引：3  

王晓丽  李鱼  王一喆  杜显元  王婷  刘建林 《吉林大学学报(地球科学版)》2010,40(1):183-187

通过考察粘土矿物及掺杂粘土矿物前后沉积物的吸附/解吸特性,分析了伊利石与蒙脱石对重金属污染沉积物中Cu与Zn稳定固定化的可行性。结果表明：伊利石与蒙脱石的掺杂均降低了沉积物吸持Cu的能力（最大下降量分别为5.4%和3.8%）,伊利石的掺杂同样降低了沉积物吸持Zn的能力（最大下降量为4.4%）,但蒙脱石掺杂后沉积物吸持Zn的能力明显增强,最高增加5.7%。因此,蒙脱石具有固定污染沉积物中Zn的能力,但不能提高污染沉积物中Cu的稳定性。  相似文献   

河水中悬浮颗粒物对重金属的吸附行为     

夏义雄  陈华林 《亚热带资源与环境学报》2012,7(4):82-86

本研究以瓯江河水为对象,研究河水中悬浮颗粒物对重金属（Cu、Zn、Cd、Pb）离子的吸附行为．分别进行了Cu、Zn、Cd、Pb在悬浮颗粒物的吸附速率,解吸速率以及溶解性有机质（DOM）对吸附解吸行为的影响实验．结果表明：河水中悬浮颗粒物对Cu、Zn、Cd、Ph的吸附和解吸速率较快,吸附平衡时间为8h,解吸平衡时间为4h...  相似文献   

南黄海沉积物中活性铁氧化物对有机碳的保存作用     

陶婧  马伟伟  李文君  李铁  朱茂旭 《海洋学报》2017,39(8):16-24

土壤和沉积物中活性铁对有机质的吸附对有机质具有长期稳定和保存作用,从而在地质时间尺度上缓冲大气CO₂浓度。本文利用连二亚硫酸钠还原性溶解提取活性铁氧化物（FeR）及与之结合的有机碳（Fe-OC）,定量研究了南黄海沉积物中FeR与OC之间的结合方式以及FeR对OC的保存作用,讨论了深度增加对二者相互作用的影响。结果表明,南黄海沉积物中Fe-OC占沉积物总有机碳的份数（f_Fe-OC）为（13.2±7.47）%,即活性铁对OC的年吸附量为0.72 Mt,占全球边缘海沉积物TOC年埋藏通量的0.44%。Fe-OC的平均OC:Fe为4.50±2.61,表明共沉淀作用对有机质的保存起重要作用,且其比值随海源有机质含量增加而增加。Fe-OC稳定碳同位素（δ13C_Fe-OC）结果表明,FeR优先保存活性有机质,但这种选择性随OC:Fe增大而减弱。随深度增加,f_Fe-OC和δ13C_Fe-OC均未表现出显著变化,这与该海域沉积物中有机质活性较低、铁还原作用较弱有关。  相似文献   

环境因子对菲在黄河口沉积物上吸附的影响     

王建燕  王萍  李秋梅  李淑芳  张高生  陈静 《海洋科学》2017,41(5):103-109

为研究多环芳烃从河口到近海的环境归趋行为与生态风险,考察了沉积物质量浓度、溶解性有机质、温度、盐度4种典型环境因子对菲在黄河口沉积物上吸附的影响,比较了黄河口与近海两种沉积物对菲的吸附性能。研究结果表明,沉积物质量浓度越低,单位质量颗粒物的菲吸附量越高;共存的溶解性有机质对菲的吸附具有增促作用,且腐殖酸比黄腐酸的作用更显著;温度的升高不利于菲的吸附,而盐度的增加有利于菲的吸附。菲在沉积物上的吸附是分配作用与表面吸附两种行为的耦合,其中黄河口沉积物以表面吸附为主,而近海沉积物以分配作用为主。近海沉积物菲吸附量显著高于黄河口沉积物菲吸附量。基于此,菲从河口到近海的迁移过程中,更易于在沉积物表面发生吸附沉降,从而可能降低水相中的生态危害,但对近海底栖生物具有潜在的健康生态风险。  相似文献   

Microbial activity promotes the enrichment of cobalt over nickel on hydrogenetic ferromanganese crusts     

P. P. Sujith  D. Ramanan  P. A. LokaBharathi 《Marine Georesources & Geotechnology》2017,35(8):1158-1167

The different mineral phases of the ferromanganese (Fe–Mn) crusts stem from the interaction of biotic and abiotic components. It is therefore vital to study the activity of these components to decipher their contribution to the enrichment/depletion of metals in the crust. Thus, the present study examined sorption and release of Co and Ni by Fe-Mn crusts with associated microbial communities in the presence and absence of the metabolic poison sodium azide (15?mM). The study was conducted in the presence (G⁺) and absence (G^?) of added glucose (0.1%) at temperatures of 4?±?1°C and 28?±?2°C. Results showed that the microbial community had maximal sorption of Co of 66.12?µg?g^?1 at 4?±?1°C in the absence of added glucose and 479.75?µg?g^?1 at 28?±?2°C in the presence of added glucose. Maximum sorption of Ni in the absence of added glucose was 1.89?µg?g^?1 at 4?±?1°C and release of Ni was 51.28?µg?g^?1 in the presence of added glucose. Under abiotic conditions with 15?mM sodium azide as a metabolic inhibitor, significant amounts of Co and Ni were released in the G⁺ medium. Total cell counts on the Fe-Mn crust in the presence of added glucose increased by an order of magnitude from 10⁶ to 10⁷ cells g^?1 and in the absence of added glucose remained within the order of 10⁶ cells?g^?1 irrespective of temperature of incubation. Microscopic observation of the samples from biotic incubations showed numerous bacterial cells, exopolysaccharides, and structures resembling secondary minerals formed by bacteria. The results indicate that bacteria promote the enrichment of Co and Ni on the hydrogenetic Fe-Mn crusts by sorption processes and release of Ni by reductive dissolution of the oxides. The higher enrichment of Co than Ni is attributed to the way in which microbes interact with the metals.  相似文献   

On the cumulant expansion up scaling of ground water contaminant transport equation with nonequilibrium sorption     

Hakan Sirin  Miguel A. Mariño 《Stochastic Environmental Research and Risk Assessment (SERRA)》2008,22(4):551-565

The laboratory-scale ground water transport equation with nonequilibrium sorption reaction subjected to unsteady, nondivergence-free, and nonstationary velocity fields is up-scaled to the field-scale by using the ensemble-averaged equations obtained from the cumulant expansion ensemble-averaging method. It is found that existing ensemble-averaged equations obtained with the help of the cumulant expansion method for the system of linear partial differential equations are not second-order exact. Although the cumulant expansion methodology is designed for noncommuting operators, it is found that there are still commudativity requirements that need to be satisfied by the functions and constants exist in the coefficient matrix of the system of ordinary/partial differential equations. A reversibility requirement, which covers the commudativity requirements, is also proposed when applying the cumulant expansion method to a system of partial differential equations/a partial differential equation. The significance of the new velocity correction obtained in this study due to the applied second-order exact cumulant expansion is investigated on a numerical example with a linear trend in the distribution coefficient. It is found that the effect of the new velocity correction can be significant enough to affect the maximum concentration values and the plume center of mass in the case of a trending distribution coefficient in a physically heterogeneous environment.  相似文献   

Equilibrium Modeling of Arsenic Adsorption in a Ternary Arsenic–Iron Oxide–Natural Organic Matter System          下载免费PDF全文

Hoda Fakour  Tsair‐Fuh Lin  Shang‐Lien Lo 《洁净——土壤、空气、水》2016,44(10):1287-1295

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Sorption model for dissolved and particulate aluminium in the Conway estuary, UK   总被引：1，自引：0，他引：1  

S. Upadhyay   《Estuarine, Coastal and Shelf Science》2008,76(4):914-919

Dissolved Al carried in river water apparently undergoes a fractional removal at the early stages of mixing in the Conway estuary. On the other hand, dissolved Al behaves almost conservatively in high salinity (>13) estuarine waters. In order to understand the geochemistry of Al in these estuarine waters, simple empirical sorption models have been used. Partitioning of Al occurs between solid and solution phases with a distribution coefficient, K_d, which varies from 0.67 × 10⁵ to 3.38 × 10⁶ ml g⁻¹ for suspended particle concentrations of 2–64 mg l⁻¹. The K_d values in general decrease with increasing suspended particulate matter and this tendency termed the “particle concentration effect” is quite pronounced in these waters. The sorption model derived by previous workers for predicting concentrations of dissolved Al with changing suspended sediment loads has been applied to these data. Reasonable fits are obtained for K_d values of 10⁵, 10⁶ and 10⁷ ml g⁻¹ with various values of α. Further, a sorption model is proposed for particulate Al concentrations in these waters that fits the data extremely well defined by a zone with K_d value 10⁷ ml g⁻¹ and C₀ values 16 × 10⁻⁶ mg ml⁻¹ and 92 × 10⁻⁶ mg ml⁻¹. These observations provide strong evidence of sorption processes as key mechanisms influencing the distribution of dissolved and particulate Al in the Conway estuary and present new insight into Al geochemistry in estuaries.  相似文献   

膨胀石墨吸附重油的热力学研究     

曹晓燕  魏淑伟  杨桂朋  周立敏 《中国海洋大学学报(自然科学版)》2008,38(1):103-106

研究膨胀石墨对模拟海水中重油的吸附热力学行为.结果表明:在293～308 K,含油量为2.172～18.11 mg·dm-3实验浓度范围内,膨胀石墨对模拟海水中重油的吸附是放热过程,吸附等温线符合Freundlich和Langmuir方程.根据热力学函数关系计算出膨胀石墨对模拟海水中重油的标准吸附焓变为-39.49 kJ·mol-1,标准吉布斯自由能变为-22.40～-23.50 kJ·mol-1,说明吸附过程可自发进行.  相似文献