地气测量研究现状及其影响因素

地气测量是寻找深部隐伏矿床的一种化探新方法，目前这一方法已在许多国家和地区应用并迅速发展，作者着重综述了地气测量的研究历史、现状及存在的问题，指出了季节的变化、土壤中氢氧化铁及温度与pH值对纳米微料的吸附作用等问题，是地气测量效果的显著影响因素。     

磷块岩对二价镉离子的吸附性能研究

用宜昌、海口、保康等地磷块岩对水溶液中镉离子的吸附实验结果表明，影响吸附效果的主要因素有介质的酸度，作用时间，初始Cd^2 浓度和样品用量。在pH=6，作用时间为15min，初始Cd^2 浓度为30mg/L的实验条件下，宜昌硅质磷块岩对镉离子的去除率可达98％，去除容量为4．5mg/g（样品），吸附效果最好，海口的效果次之，而保康钙质磷块岩的效果最差。上述差异可能与这些磷块岩的矿物成分和结晶化学特性之间的差异有关。     

纳米粒子－胶体溶液－吸附作用——对某些金属矿床成因的探讨

根据物质呈纳米级状态时，其物理性质发生显著的变化，认为由其作为分散相分散于不同的分散介质（气体、液体和固体）中所构成的气溶胶、胶体溶液或固体溶胶，尤其是胶体溶液对运移成矿物质尤为重要，而对于被运移的胶粒来说，自身凝聚或被其他载体矿物或岩石的吸附富集将是一种重要的成矿作用，这特别有助于解释微细浸染型金矿、砂金矿及某些稀有及分散元素矿床的成因。     

烃类的化学吸附作用对岩石剩磁稳定性的影响

通过对细粒天然磁铁矿的穆斯堡尔谱研究和对华北冀东油田第三系砂岩样品的磁性载体成分、成因、剩磁稳定性和特征剩磁方向的研究，探讨了烃类的化学吸附作用与岩石剩磁稳定性之间的关系，烃类的化学吸附作用能够降低岩石的剩磁稳定性，因此，可能会导致产生次生剩磁。这一认识为客观全面地了解各种次生剩磁的成因、研究重磁化现象的时空分布规律，进而为探索新的磁清洗方法和应用岩石磁学方法研究含油气地层的地质问题提供了新的思路     

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.     

Influence of plant on the extractability of estrogen in the rhizospheric soil

Livestock wastes applied to agricultural land are potential sources of steroidal hormones （estradiol （E2）, estrone （E1）, and estriol （E3）） that can adversely affect the aquatic ecosystem as endocrine disruptors. But the effects of plants on the fate of estrogen in the environment are not clearly known. In the present report, the behavior of E1, E2 and E3 added to the rhizospheric soil in various concentrations and its effect on plant growth were examined by estrogen batch sorption test, plant pot test and estrogen extraction test. Trifolium repens was grown on the soil spiked with E2 or a mixture of E1, E2 and E3. Pots without plant were prepared as controls. All pots were watered in 50 ml dose almost every day, and the rhizosheric soil and plant body were collected 7, 19, 26, 33 days after planting. The soil was sequentially extracted with Milli-Q water, and methanol / 1M acetic acid solvent followed by methanol wash at the solid to liquid ratio of 1 ： 4 （g/mL）. Extracts were analyzed for El, E2 and E3 using a Shimadzu GCMS-QP5050. Plant dry weight （4 hours, 105 ℃） was measured as an indicator of plant growth. In batch sorption tests, E1 and E2 concentrations in the liquid phase significantly decreased within 24 hours after the addition of estrogen. The sum of methanol / 1M acetic acid extractable E 1 and E2 in the soil decreased to half of the initial added amount within 7 days. Reduction in total estrogenic activity of the soil extracts （estimated as 0.01CE1＋CE2＋0.1CE3 where CE1, CE2 and CE3 are respective El, E2 and E3 concentrations per unit soil weight） continued for 1 month due to slow oxidation of E2 to E1. Desorption of E2 from soil during the pot experiment was higher than expected from the sorption experiment.     

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）.     

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.     

Heavy metal retention by soil mineral phases during a potential soil contamination by sewage sludge

The immobilization conditions of heavy metals （Ni, Cu, Zn, Pb） potentially released from sewage sludge to soils were examined. Competitive adsorption experiments, sequential extraction and analytical electron microscopic studies were performed on soils with different compositional characteristics to gain information about the interaction and association of metals with soil minerals. The results showed that Cu and Pb can be characterized by a preferred adsorption in contrast to Zn and Ni independent of initial metal concentrations, ratios, and soil composition. Precipitation is the dominating retardation process in the sample containing carbonates, but it is also characteristic of metals with inhibited adsorption in samples free of carbonate. Both Cu and Pb show high affinity towards organic matter. Differences in metal affinities towards different clay minerals show the immobilization of Cu rather by specific adsorption and that of Pb rather by ion exchange. According to the sequential extraction studies the role of ion exchange is the most important process for the retardation of Zn, and in the sample containing montmorillonite. The specific adsorption is significant mostly for Cu and Pb, and primarily in samples rich in organic matter and containing vermiculite. The co-precipitation of metals with Fe-Mn oxides is significant primarily for Cu, but in some cases Pb and Zn can be also found in this fraction. In general, the strength of immobilization for the studied metals is as follows： Cu〉Pb〉Zn〉Ni. Significantly higher metal adsorption was found by the phases in the sample containing carbonates, as well as in samples characterized by the close association of clay minerals and iron oxides. Smectite and vermiculite are the most important adsorbents in soils for all of the metals. Additionally, iron-oxides immboilize significant amounts of Cu and Zn, too.     

Effect of incubating plant cuticles in soil on their sorptive capabilities

Sorption and desorption are the major processes influencing the fate of hydrophobic organic compounds （HOCs） in soils. Among the natural sorbents in the environment, soil organic matter （SOM） plays a significant role in the overall sorption of many organic compounds. Recently, several reports have emphasized the role of aliphatic-rich sorbents in the binding of HOCs. The main source of aliphatic compounds for SOM is biopolymers derived from above- and below-ground plant cuticular matter. The plant cuticle is a thin layer of predominantly lipid material that covers all primary aerial surfaces of vascular plants. The objective of this study was to examine the effect of decomposition and transformation of plant cuticles on their sorption behavior with triazine herbicides and polycyclic aromatic hydrocarbons （PAHs）. Sorption-desorption behavior was studied during 12 months of incubation of cuticles isolated from tomato fruits and pummelo leaves in sandy soil. Sorption and desorption experiments and spectroscopic and chemical analyses were performed using the samples after 0, 1, 3, 6 and 12 months of incubation. The decomposition of the cuticles （46-49% after 12 months） did not affect the organic carbon-normalized Freundlich distribution coefficient （KFOC） for the PAHs. In addition, throughout the incubation period, the two PAHs exhibited linear and reversible sorption isotherms with both cuticles. However, the isotherms of the triazines were significantly affected by the decomposition of the cuticles from pummelo leaves, whereas only minor changes were recorded for the tomato cuticle samples. For the microcosm with cuticles from the pummelo leaves, the KFOC values of the triazines increased with increasing decomposition.