Sulfuric acid as a weathering agent of carbonate weathering constrained by δ^13C： Examples from Southwest China

Rock weathering by carbonic acid is one of the important atmosphere CO2 sequestration. Actually, it depends on whether carbonic acid or other acids as weathering agents, which is important to understand the model of global carbon cycle. For example, sulfuric acid derived from oxidation of pyrite takes part in the rock weathering, which might counteract one part of CO2 drawdown by silicate weathering. In this study, chemicals and carbon isotopic composition of waters were determined in the Beipan River, Guizhou. The δ^13C values of dissolved inorganic carbon in the province, Southwest China. The values of the samples range from -13.1‰ to -2.4‰, which show a good negative correlation with the equivalent ratio of [HCO3]/（[Ca^2＋＋Mg^2＋]） and a good positive correlation with the equivalent ratio of [SO4^2-]/（[Ca^2＋＋Mg^2＋]） and [SO4^2-]/[HCO3^-]. The relationships suggest that sulfuric acid took part in carbonate weathering. Acid rain is thus a significant source of sulfuric acid to the karstic rivers of Guizhou Province.     

Pretreatment of diosgenin wastewaters using polyferric sulfate as a main coagulant

Diosgenin is produced from Dioscrea L, mainly using D.zingiberensis as the raw material. During the process, particularly in the process of acidic hydrolysis, large quantities of high-strength wastewaters are discharged. The waste liquids are characteristic of strong acidity, usually with pH value less than 1, and high concentrations of organic matter with average CODcr （chemical organic demand） in the range of 20000-3000 mg/L. Without proper treatment, their free disposal would pose serious threat to natural ecosystem and cause considerable environmental problems. Since diosgenin wastewaters contain high load organics and acidity, appropriate pretreatment is needed before they are biologically degraded. Coagulation is a common method for eliminating colloid particles and/or high molecule organic chemicals from wastewaters. Poly-ferric sulfate is found to be most effective in removing organic matter. The objective of this study is to investigate the effectiveness and feasibility of poly-ferric sulfate to reduce CODcr and turbidity from diosgenin wastewaters. Due to its high acidic nature, the pH value of diosgenin wastewater was neutralized with Ca（OH）2 solution before being coagulated. Various factors that influence the coagulation process, such as pH value, the dosage of poly-ferric sulfate, polyelectrolyte aids and mixing conditions were examined in the experiments.     

Chemical Assessment of Oceanic and Terrestrial Sulfur in the Marine Boundary Layer over the Northern North Pacific during Summer

Dimethylsulfide (DMS) in surface seawater and the air, methanesulfonic acid (MSA) and non-sea-salt sulfate (nss-SO₄ ²–) in aerosol, and radon-222 (Rn-222) were measured in the northern North Pacific, including the Bering Sea, during summer (13 July – 6 September 1997). The mean atmospheric DMS concentrations in the eastern region (21.0 ± 5.8 nmole/m³ (mean ± S.D.), n=30) and Bering Sea (19.9 ± 9.8 nmole/m³, n=10) were higher than that in the western region (11.1 ± 6.4 nmole/m³, n=31) (p<0.05), although these regions did not significantly differ in the mean DMS concentration in surface seawater. Mean sea-to-air DMS flux in the eastern region (21.0 ± 10.4 mole/m²/day, n=19) was larger than those in the western region (11.3 ± 16.9 mole /m²/day, n=22) and Bering Sea (11.2 ± 7.8 mole/m²/day, n=7) (p<0.05). This suggests that the longitudinal difference in atmospheric DMS was produced by that in DMS flux owing to wind speed, while the possible causes of the higher DMS concentrations in the Bering Sea include (1) later DMS oxidation rates, (2) lower heights of the marine boundary layer, and (3) more inactive convection. The mean MSA concentrations in the eastern region (1.18 ± 0.84 nmole/m³, n=35) and Bering Sea (1.17 ± 0.87 nmole/m³, n=13) were higher than that in the western region (0.49 ± 0.25 nmole/m³, n=28) (p < 0.05). Thus the distribution of MSA was similar to that of DMS, while the nss-SO₄ ²– concentrations were higher near the continent. This suggests that nss-SO₄ ²– concentrations were regionally influenced by anthropogenic sulfur input, because the distribution of nss-SO₄ ²– was similar to that of Rn-222 used as a tracer of continental air masses.     

等离子体发射光谱法测定重晶石中钡铁和硅

重晶石经Ｎａ２ＣＯ３熔融,水浸取,过滤。沉淀经ＨＣｌ溶解后,用电感耦合等离子体发射光谱法同时测定主成分ＢａＳＯ４和次量成分Ｆｅ２Ｏ３以及滤液中的ＳｉＯ２,结果与部颁标准方法符合。方法精密度好,主量组分ＢａＳＯ４测定的ＲＳＤ（ｎ＝６）为０．２４％,次量组分Ｆｅ２Ｏ３和ＳｉＯ２的ＲＳＤ（ｎ＝６）分别是３．６９％和１．４５％。     

溶剂萃取法制取硫酸钾中试及其新进展

描述了用工业硫酸和氯化钾为原料,萃取法制取硫酸钾新工艺及其工程化的新进展。研究了该工艺三相萃取过程的基本原理,列出了试验数据及经济技术评价。     

用含铝矿石生产硫酸铝的工艺

本文用含铝矿石生产硫酸铝。在反复试验的基础上所拟定的最佳工艺流程，经建厂投产质量达标。并对工艺条件和影响质量因素进行了有效的探索。     

Reservoir geochemistry of South Pass 61 Field, Gulf of Mexico: compositional heterogeneities reflecting filling history and biodegradation

Cluster analysis of GC data for gasoline and mid-range hydrocarbon ratios from fifty-one South Pass 61 Field oils reveals geochemically similar oil clusters corresponding to geographically coherent groups. Insight into the groupings is obtained from examination of indicators of geochemical processes, e.g., anaerobic biodegradation, aerobic biodegradation and extensive remigration of light ends. Six duplicate samples collected in 1986 and 1992 as well as replicate runs on a single sample showed excellent analytical reproducibility.Subtle but consistent differences in both gasoline and oil-range hydrocarbon maturity indicators are observed between the east, west, and far west flanks of the field, suggesting filling of different segments of the reservoir from different kitchens at slightly different stages of thermal maturity or with slightly different chemical character. The west flank of the salt dome was charged with slightly more thermally mature petroleum than the east flank. The stratigraphically oldest and deepest sand on the far west flank has received the most mature petroleum. Different fluid contacts and GORs are observed in different sands and different fault blocks. The stacked pay geometry of the field and widespread faulting have led to considerable remigration of gas and condensate as observed in other fields in the Gulf of Mexico (Thompson, 1987).Biodegradation varies in severity with depth and reservoir zone, but is frequently overprinted by remigration of light end hydrocarbons. Anaerobic biodegradation by sulfate-reducing bacteria is probably the cause of light to moderate alteration in intermediate depth Pliocene sands which are hydraulically connected to the salt dome (with dissolution of anhydrite from the salt dome providing the sulfate). Widespread late pyrite formation in reservoir sandstones is inferred to represent the ultimate sink for reduced sulfur from sulfate reduction during oil biodegradation. Co-produced water compositions suggest no oxygenated freshwater infusion.     

Nitrate in the atmospheric boundary layer of the tropical South Pacific: Implications regarding sources and transport

Weekly bulk aerosol samples collected at Funafuti, Tuvalu (8°30S, 179°12E), American Samoa (14°15S, 170°35W), and Rarotonga (21°15S, 159°45W), from 1983 through most of 1987 have been analyzed for nitrate and other constituents. The mean nitrate concentration is about 0.11 g m^–3 at each of these stations: 0.107±0.011 g m^–3 at Funafuti; 0.116±0.008 at American Samoa; and 0.117±0.010 at Rarotonga. Previous measurements of mineral aerosol and trace metal concentrations at American Samoa are among the lowest ever recorded for the near-surface troposphere and indicate that this region is minimally affected by transport of soil material and pollutants from the continents. Consequently, the nitrate concentration of 0.11 g m^–3 can be regarded as the natural level for the remote marine boundary layer of the tropical South Pacific Ocean. In contrast, over the tropical North Pacific which is significantly impacted by the transport of material from Asia and North America, the mean nitrate concentrations are about three times higher, 0.29 and 0.36 g m^–3 at Midway and Oahu, respectively. The major sources of the nitrate over the tropical South Pacific are still very uncertain. A very significant correlation between the nitrate concentrations at American Samoa and the concentrations of ²¹⁰Pb suggests that transport from continental sources might be important. This continental source could be lightning, which occurs most frequently over the tropical continents. A near-zero correlation with ⁷Be indicates that the stratosphere and upper troposphere are probably not the major sources. A significant biogenic source would be consistent with the higher mean nitrate concentrations, 0.16 to 0.17 g m^–3, found over the equatorial Pacific at Fanning Island (3°55N, 159°20W) and Nauru (0°32S, 166°57E). The lack of correlation between nitrate and nss sulfate at American Samoa does not necessarily preclude an important role for marine biogenic sources.     

Possible Carbonate Origin of Ore Sulfur from Geumseong Mo Deposit, South Korea

Abstract: In order to know the cause of the high δ³⁴S values of the Korean ore deposits (Ishihara et al., 2000), Geumseong molybdenum skarn deposit and related Jurassic granitoids and Cambro-Ordovician carbonates were selected for the δ³⁴S analyses. Two sulfide samples occurring in hydrothermal veins in fresh granitoids quarry at Songhaksan yielded δ³⁴S values of +6.9 and +8.8 permil. These are slightly higher than +5.3 permil δ³⁴S of the averaged rock sulfides for the Jurassic Daebo granitoids. Pyrite and molybdenite from the Geumseong deposit vary from +8.6 to +11.5 permil (average + 10.7 permil). The intruded carbonates contain very low amount of SSS (structurally substituted sulfate) as 2.9 to 8.1 ppm with high δ³⁴S values between +28.8 and + 40.0 permil, and sulfides sulfur of 52 to 779 ppm with variable δ³⁴S values between +3.2 and +22.5 per–mil. It is concluded that sulfur of the host carbonates was extracted and migrated into the skarn deposit at the time of the granitoid intrusion and the related hydrothermal convection, on the basis of the location of the skarn deposit occurring between the carbonates and Jurassic granitoids, and of very low contents of SSS sulfur in the carbonates. A part of SSS possibly contaminated into the Jurassic granite.     

Comparison of methods for calculating annual solute exports from six forested appalachian watersheds

Six methods were compared for calculating annual stream exports of sulfate, nitrate, calcium, magnesium and aluminum from six small Appalachian watersheds. Approximately 250–400 stream samples and concurrent stream flow measurements were collected during baseflows and storm flows for the 1989 water year at five Pennsylvania watersheds and during the 1989–1992 water years at a West Virginia watershed. Continuous stream flow records were also collected at each watershed. Solute exports were calculated from the complete data set using six different scenarios ranging from instantaneous monthly measurements of stream chemistry and stream flow, to intensive monitoring of storm flow events and multiple regression equations. The results for five of the methods were compared with the regression method because statistically significant models were developed and the regression equations allowed for prediction of solute concentrations during unsampled storm flows. Results indicated that continuous stream flow measurement was critical to producing exports within 10% of regression estimates. For solutes whose concentrations were not correlated strongly with stream flow, weekly grab samples combined with continuous records of stream flow were sufficient to produce export estimates within 10% of the regression method. For solutes whose concentrations were correlated strongly with stream flow, more intensive sampling during storm flows or the use of multiple regression equations were the most appropriate methods, especially for watersheds where stream flows changed most quickly. Concentration–stream flow relationships, stream hydrological response, available resources and required level of accuracy of chemical budgets should be considered when choosing a method for calculating solute exports. © 1997 John Wiley & Sons, Ltd.