Arsenic strongly associates with ferrihydrite colloids formed in a soil effluent

Arsenic mobility may increase in liquid phase due to association with colloidal Fe oxides. We studied the association of As with Fe oxide colloids in the effluent from water-saturated soil columns run under anoxic conditions. Upon exfiltration, the solutions, which contained Fe²⁺, were re-aerated and ferrihydrite colloids precipitated. The entire amount of effluent As was associated with the ferrihydrite colloids, although PO₄³⁻, SiO₄⁴⁻, CO₃²⁻ and dissolved organic matter were present in the effluent during ferrihydrite colloid formation. Furthermore, no subsequent release of As from the ferrihydrite colloids was observed despite the presence of these (in)organic species known to compete with As for adsorption on Fe oxides. Arsenic was bound via inner-sphere complexation on the ferrihydrite surface. FTIR spectroscopy also revealed adsorption of PO₄³⁻ and polymerized silica. However, these species could not impede the quantitative association of As with colloidal ferrihydrite in the soil effluents.     

池州市碳酸钙资源开发现状和发展措施

介绍了国内外碳酸钙行业生产、应用技术发展现状和池州市碳酸钙资源开发现状，找出了池州市碳酸钙资源开发中存在的问题和解决措施，提出了池州市碳酸钙工业发展需要实施的各种措施。     

Hollow TiO2 spheres with improved visible light photocatalytic activity synergistically enhanced by multi-stimulative: Morphology advantage, carbonate-doping and the induced Ti3 +

Great efforts have been devoted to improve the photocatalytic activity of TiO_2 in the visible light region. Rational design of the external structure and adjustment of intrinsic electronic status by impurity doping are two main effective ways to achieve this purpose. A facile onepot synthetic approach was developed to prepare C-doped hollow TiO_2 spheres, which simultaneously realized these advantages. The synthesized TiO_2 exhibits a mesoporous hollow spherical structure composed of fine nanocrystals, leading to high specific surface area(~180 m~2/g) and versatile porous texture. Carbonate-doping was achieved by a postthermal treatment at a relatively low temperature(200°C), which makes the absorption edge red-shifted to the visible region of the solar spectrum. Concomitantly, Ti~(3+) induced by C-doping also functions in improving the visible-light photocatalytic activity by reducing the band gap. There exists a synergistic effect from multiple stimulatives to enhance the photocatalytic effect of the prepared TiO_2 catalyst. It is not out of expectation that the asprepared C-doped hollow TiO_2 spheres exhibits an improved photocatalytic activity under visible light irradiation in organic pollutant degradation.     

Management of basiphilous dune slack communities in relation to carbonate accumulation and hydrological conditions

In dune slacks in The Netherlands, a decline of rare mesotrophic basiphilous plant species and their plant communities has been observed in combination with an increase of more productive systems with common, taller acidophilous plant species. This has been attributed to both natural and anthropogenic changes. In a humid climate with a precipitation surplus, as in The Netherlands, the calcium carbonate content of a calcareous soil increases with depth. However, soils in coastal dune slacks, may have a higher carbonate content in the topsoil horizon than in the underlying layers. Carbonates which buffer the pH can prolong the presence of mesotrophic basiphilous plant communities which are of high conservation value. To explain the occurrence of calcareous surface horizons in dune slacks, hydrological and micromorphological analyses were carried out in three dune slacks. Two slacks are situated on the Wadden Sea islands in the northern part of The Netherlands; one on Schiermonnikoog and one on Texel. The third slack is situated in the dunes on the island of Goeree in the southwestern part of The Netherlands. In all three slacks, carbonate occurs as mollusc and gastropod fragments (silt- or sand-sized) and as micritic nodules in the topsoil layer, due to aeolian deposition and sedimentation by water.In situ carbonate accumulation (calcitans and calcareous crusts) due to CO₂ release in inundated and/or capillary rise of calcareous groundwater near, or at the soil surface. Accumulation of carbonate also occurs as a result of biological activity by algae in the topsoil of the Goeree site. In general, hydrological processes maintaining high levels of calcareous groundwater are a prerequisite for the maintenance of high carbonate levels in topsoils. Such levels are necessary for the conservation and management of basiphilous pioneer vegetation.     

Impact of urbanization on hydrochemical evolution of groundwater and on unsaturated-zone gas composition in the coastal city of Tel Aviv, Israel

The coastal city of Tel Aviv was founded at the beginning of the 20th century. The number of its inhabitants and its water consumption increased rapidly. This study analyses a 15-year record (1934-1948) of pre-industrial development of groundwater chemistry in the urban area. Archive data on concentrations of major ions, dissolved gases (CO2 and O2), organic matter, and pH were available for each half-year during the period of 1934-1948. The major factors causing changes in the chemistry of groundwater flowing in three sandy sub-aquifers have been seawater encroachment due to overpumping, and infiltration of effluents from pit-latrine collectors. Influence of these factors decreases with depth. Landward-penetrating seawater passed through clayey coastal sediments, interbedded among sands and calcareous sandstones, and spread into the Kurkar Group aquifer. This has led to exchange of sodium (dominant in seawater) with calcium adsorbed on clay particles, enriching groundwater with calcium. Intensity of cation exchange decreases inland and with depth. Infiltration of pit-latrine effluents has introduced large amounts of ammonium into the unsaturated zone. Its rapid oxidation in unsaturated sediments has caused massive nitrate production, accompanied by pore-water acidification. This process induces dissolution of vadose carbonate, resulting in enrichment of groundwater recharge in calcium. Anthropogenically induced dissolution of calcite in the unsaturated zone has been the major factor for the increase of Ca2+ concentration in groundwater, accounting for about 80% of this increase. In the interface zone, an additional 20% of calcium has been supplied by cation exchange. Owing to pH increase caused by denitrification in the aquifer, Ca(2+)-rich waters supersaturated with calcite could be formed, especially in the capillary fringe of the uppermost sub-aquifer, which could induce calcite precipitation and ultimately lead to the cementation of sandy aquifers. Urban development has caused drastic changes in the gas content in the unsaturated zone and in groundwater. Carbon dioxide was intensively generated by nitrification-denitrification processes, by hydration of urea, to a lesser degree by oxidation of organic matter, and probably by anoxic biodegradation of organics. Between 1934 and 1948, concentrations of CO2 in unsaturated sediment air rose from 3.2% to 7.6%. In the unsaturated zone, oxygen consumption for oxidation of ammonium and organic matter lowered O2 concentrations in sediment air to unusually low values of 3.9-12.9%. Nitrification in the urban unsaturated zone could thus serve as a pump, sucking in atmospheric oxygen at a rate of about 0.3-0.5 g m-2 day-1. The extreme concentrations of CO2 and O2 in unsaturated sediments have been preserved due to production and consumption of gas under conditions of diminishing areas open to the atmosphere, uncovered by buildings and by roads.     

RETENTION BASIN FAILURES IN CARBONATE TERRANES1

ABSTRACT Sinkholes and subsidence in areas subject to dewatering of carbonate formations have been documented in several geologic and hydrologic investigations. Excessive ground-water pumpage has been cited as a causative factor in areas of increased sinkhole activity. Subsurface erosion of unconsolidated materials underlain by carbonate rocks is one cause of the collapses. Infiltrating water from retention basins may cause subsurface erosion and eventual failure by collapse of the structure. The resulting ground-water contamination would be great as the pollutants spread throughout the solution-cavity system.     

离子色谱法测定碳酸锶产品中的氯杂质

讨论了在单柱离子色谱仪上用ＴＳＫｇｅｌＩＣ－Ａｎｉｏｎ－ＳＥ柱为分离柱,１ｍｍｏｌ／Ｌ邻苯二到（ＰＨ５．４）作流动相,以电导检测器检测,测定沸水提取碳酸锶产品中的杂质氯的方法。该法简便、快速、准确、无干扰,在测定范围内有良好的线性。最小检出量为０．１μｇ,ＩＣ法与比色法的测定结果基本一致,ＣＩ＾－的含量为０．１６６％,相对标准偏差为２．８％,回收率为９７．９％～１００％。     

Is the availability of different nutrients a critical factor for the impact of bacteria on subterraneous carbon budgets?

Bacteria thriving in underground systems, such as karsts, adapt to use a variety of nutrients. Most of these nutrients derive from superficial processes. This study shows that bacteria are able to differentially induce carbonate precipitation or dissolution depending on the availability of nutrients for growth. Different bacterial strains isolated from caves, representing the most common components of these microbial communities, were cultured with different carbon and nitrogen sources (e.g., acetate, glucose, peptone, humic acids) and induced changes in pH were measured during growth. Carbonate can either precipitate or dissolve during bacterial growth. The induction of carbonate precipitates or their dissolution as a function of consumption of specific carbon sources revealed the existence of an active nutrient cycling process in karsts and links nutrients and environmental conditions to the existence of a highly significant carbon sink in subterraneous environments.     

Effects of initial iron corrosion rate on long-term performance of iron permeable reactive barriers: Column experiments and numerical simulation

Column experiments and numerical simulation were conducted to test the hypothesis that iron material having a high corrosion rate is not beneficial for the long-term performance of iron permeable reactive barriers (PRBs) because of faster passivation of iron and greater porosity loss close to the influent face of the PRBs. Four iron materials (Connelly, Gotthart-Maier, Peerless, and ISPAT) were used for the column experiments, and the changes in reactivity toward cis-dichloroethene (cis-DCE) degradation in the presence of dissolved CaCO₃ were evaluated. The experimental results showed that the difference in distribution of the accumulated precipitates, resulting from differences in iron corrosion rate, caused a difference in the migration rate of the cis-DCE profiles and a significant difference in the pattern of passivation, indicating a faster passivation in the region close to the influent end for the material having a higher corrosion rate. For the numerical simulation, the accumulation of secondary minerals and reactivity loss of iron were coupled using an empirically-derived relationship that was incorporated into a multi-component reactive transport model. The simulation results provided a reasonable representation of the evolution of iron reactivity toward cis-DCE treatment and the changes in geochemical conditions for each material, consistent with the observed data. The simulations for long-term performance were also conducted to further test the hypothesis and predict the differences in performance over a period of 40 years under typical groundwater conditions. The predictions showed that the cases of higher iron corrosion rates had earlier cis-DCE breakthrough and more reduction in porosity starting from near the influent face, due to more accumulation of carbonate minerals in that region. Therefore, both the experimental and simulation results appear to support the hypothesis and suggest that reactivity changes of iron materials resulting from evolution of geochemical conditions should be considered in the design of iron PRBs.     

Phosphate enrichment in the northern Gulf of Aqaba: Regulation by carbonate sediments and impact on nitrogen elevation

The effect of carbonate sediment in regulating phosphate concentrations in sea water was investigated by laboratory incubation experiments using different sediment types. Incubation experiments were made with two types of sediments: uncontaminated sediment from a marine reserve and contaminated sediment with deposited phosphate powders. Fluxes of inorganic nitrogen and phosphate were estimated from linear regressions of solute concentrations over incubation periods. Ammonium and phosphate fluxes were about twofold higher in the uncontaminated sediment that had significantly lower organic carbon and total phosphate concentrations than in the phosphate-contaminated sediment. To test the effect of dissolved phosphate on increasing nitrogen fixation, additional incubation experiments were carried out using treated carbonate and silicate sediments with added dissolved phosphate (20 μM). Incubations were made under sterile conditions with HgCl₂ added to distinguish between biologically enhanced processes and pure physicochemical processes. The adsorption rate of phosphate onto carbonate sediment was about twice that onto silicate sediments. No nitrogen elevation either as ammonium or as nitrate was observed in the soluble phosphate enrichment incubations. In conclusion, this study demonstrates the importance of the regulation of soluble phosphate concentrations in carbonate sediment environments where the carbonate sediment acts as a buffering system keeping soluble phosphate concentrations at certain steady-state levels. The study also demonstrates the lack of evidence on enhancement of nitrogen concentrations due to the increase phosphate concentrations.