Some breakage characteristics of ultra-fine wet grinding with a centrifugal mill

A centrifugal mill is a high-power intensity media mill that can be used for ultra-fine grinding, employing centrifugal forces generated by gyration of the axis of the mill tube in a circle. The mill charge motion is quite different depending on the ratio of the gyration diameter to the mill diameter (G / D ratio), varying from a motion similar to that of a conventional tumbling media mill to that of a vibration mill. In this study, a centrifugal mill was constructed with an arrangement where the gyration diameter could be readily adjusted. The batch grinding characteristics of three different minerals (limestone, talc and illite) in water with dispersing agent were investigated at various G / D ratios. It was found that the optimum G / D ratio in terms of the specific energy consumption to give a desired fineness of product was different for the three minerals. This was due to their different reactions to the breakage mechanisms provided by the mill charge motion at varying G / D ratios. The size distributions became progressively narrower at increased grinding times, and particles finer than about 0.1 μm were not detected even for prolonged grinding times. Measurement of specific surface areas indicated that this was not due to an artifact of the size measurements by laser diffractometry. This implies that there is a limitation in which particles finer than 0.1 μm are not produced under the conditions tested in this type of mill, but further investigation is needed for experimental verification of this limit of comminution.     

Implications of Analcime Hydrothermally Formed from Na-alumino-borosilicate Glasses Containing Cs and Sr for the Stability of High-level Radioactive Waste Form

Abstract. In order to know the behaviors of radioactive elements such as cesium and strontium during a hydrothermal alteration of borosilicate glass of radioactive waste, some alumino-borosilicate glasses belonging to the systems Na₂O-Al₂O₃-B₂O₃-SiO₂-SrO, Na₂O-Al₂O₃-B₂O₃-SiO₂-Cs₂O and Na₂O-Al₂-O₃-B₂O₃-SiO₂-SrO-Cs₂O have been treated hydrothermally at 200C under a vapor pressure of 1.54 MPa. The result shows that all glasses are changed into crystalline phases with running time up to 60 days, and that analcime-type zeolite is formed as a major product. The formed zeolite is shown to contain cesium and/or strontium. Considering the fact that natural zeolite occurs in wide physicochemical conditions including hydrothermal one, the analcime-type zeolite is expected to fix stably the radioactive elements in the disposal site. Since aluminum is necessary for the formation of the analcime-type zeolite, the waste glass should have aluminum as one of major components.     

Relational Agriculture: Gender,Sexuality, and Sustainability in U.S. Farming

Although 97% of U.S. farms are “family-owned,” little research examines how gender and sexual relationships – inherent in familial dynamics – influence farmers’ practices and livelihoods. Gender and sexual dynamics – shaped by race and class – affect who is considered a farmer, land management decisions, and access to resources like land, subsidies, and knowledge. We use feminist and queer lenses to illuminate how today’s agricultural gender and sexual relations are not “natural,” but when left uninterrogated are constructed in ways that harm women and queer farmers while limiting potential to develop sustainable practices. Women and queer farmers also resist, “re-orienting” gender and sexual relations in ways that expand possibilities for achieving food justice and ecological sustainability. We offer “relational agriculture” as a tool for making visible and re-orienting gender and sexual relations on farms. Relational agriculture brings sexuality into food justice and demonstrates the centrality of gender and sexuality to agricultural sustainability.     

Geology of Tok Island,Korea: eruptive and depositional processes of a shoaling to emergent island volcano

Detailed mapping of Tok Island, located in the middle of the East Sea (Sea of Japan), along with lithofacies analysis and K-Ar age determinations reveal that the island is of early to late Pliocene age and comprises eight rock units: Trachyte I, Unit P-I, Unit P-II, Trachyandesite (2.7±0.1 Ma), Unit P-III, Trachyte II (2.7±0.1 Ma), Trachyte III (2.5±0.1 Ma) and dikes in ascending stratigraphic order. Trachyte I is a mixture of coherent trachytic lavas and breccias that are interpreted to be subaqueous lavas and related hyaloclastites. Unit P-I comprises massive and inversely graded basaltic breccias which resulted from subaerial gain flows and subaqueous debris flows. A basalt clast from the unit, derived from below Trachyte I, has an age of 4.6±0.4 Ma. Unit P-II is composed of graded and stratified lapilli tuffs with the characteristics of proximal pyroclastic surge deposits. The Trachyandesite is a massive subaerial lava ponded in a volcano-tectonic depression, probably a summit crater. A pyroclastic sequence containing flattened scoria clasts (Unit P-III) and a small volume subaerial lava (Trachyte II) occur above the Trachyandesite, suggesting resumption of pyroclastic activity and lava effusion. Afterwards, shallow intrusion of magma occurred, producing Trachyte III and trachyte dikes.The eight rock units provide an example of the changing eruptive and depositional processes and resultant succession of lithofacies as a seamount builds up above sea level to form an island volcano: Trachyte I represents a wholly subaqueous and effusive stage; Units P-I and P-II represent Surtseyan and Taalian eruptive phases during an explosive transitional (subaqueous to emergent) stage; and the other rock units represent later subaerial effusive and explosive stages. Reconstruction of volcano morphology suggests that the island is a remnant of the south-western crater rim of a volcano the vent of which lies several hundred meters to the north-east.     

Distinct sedimentary processes reflected in the isotopic signatures of dolomitic concretions in the Miocene Pohang Basin (southwestern East Sea)

Dolomitic concretions in diatomaceous hemipelagic sediments of the Miocene Pohang Basin in the southwestern East Sea (Sea of Japan) preserve distinct signals of two independent sedimentary processes, which controlled the extents of isotopic compositions. Variable δ¹⁸O (−9.1‰ to +0.7‰) and high δ¹³C (+3.1‰ to +17.9‰) values suggest that the concretions formed in the methanogenic zone with alteration of the residual mid-Miocene seawater by volcanogenic sediments. Remarkable δ¹⁸O and δ¹³C values show a strong linear relationship, indicating that distinctly independent depositional processes operated during the formation of the concretions. The degree of methanogenesis was enhanced during rapid hemipelagic sedimentation of organic-rich particles, resulting in higher δ¹³C values, and the effect of volcaniclastics was diluted, maintaining the original properties of ambient mid-Miocene seawater. In contrast, lower δ¹⁸O and ⁸⁷Sr/⁸⁶Sr values characterize the effect of volcaniclastic sediments that were transported by intermittent gravity flows and interacted with mid-Miocene seawater. The input of volcaniclastic sediment probably degraded the role of methanogenesis by lowering the contents of organic matter and thereby decreased the δ¹³C values within the concretions. Isotopic signals recorded within the concretions highlight understanding of the depositional environment and evolution of the pore-water chemistry.     

Seasonal prediction of June rainfall over South China: Model assessment and statistical downscaling

The performances of various dynamical models from the Asia-Pacific Economic Cooperation(APEC) Climate Center(APCC) multi-model ensemble(MME) in predicting station-scale rainfall in South China(SC) in June were evaluated.It was found that the MME mean of model hindcasts can skillfully predict the June rainfall anomaly averaged over the SC domain.This could be related to the MME's ability in capturing the observed linkages between SC rainfall and atmospheric large-scale circulation anomalies in the Indo-Pacific region.Further assessment of station-scale June rainfall prediction based on direct model output(DMO) over 97 stations in SC revealed that the MME mean outperforms each individual model.However,poor prediction abilities in some in-land and southeastern SC stations are apparent in the MME mean and in a number of models.In order to improve the performance at those stations with poor DMO prediction skill,a station-based statistical downscaling scheme was constructed and applied to the individual and MME mean hindcast runs.For several models,this scheme can outperform DMO at more than 30 stations,because it can tap into the abilities of the models in capturing the anomalous Indo-Paciric circulation to which SC rainfall is considerably sensitive.Therefore,enhanced rainfall prediction abilities in these models should make them more useful for disaster preparedness and mitigation purposes.     

Aerobic oxidation of mackinawite (FeS) and its environmental implication for arsenic mobilization

Oxidation of mackinawite (FeS) and concurrent mobilization of arsenic were investigated as a function of pH under oxidizing conditions. At acidic pH, FeS oxidation is mainly initiated by the proton-promoted dissolution, which results in the release of Fe(II) and sulfide in the solution. While most of dissolved sulfide is volatilized before being oxidized, dissolved Fe(II) is oxidized into green rust-like precipitates and goethite (α-FeOOH). At basic pH, the development of Fe(III) (oxyhydr)oxide coating on the FeS surface inhibits the solution-phase oxidation following FeS dissolution. Instead, FeS is mostly oxidized into lepidocrocite (γ-FeOOH) via the surface-mediated oxidation without dissolution. At neutral pH, FeS is oxidized via both the solution-phase oxidation following FeS dissolution and the surface-mediated oxidation mechanisms. The mobilization of arsenic during FeS oxidation is strongly affected by FeS oxidation mechanisms. At acidic pH (and to some extent at neutral pH), the rapid FeS dissolution and the slow precipitation of Fe (oxyhydr)oxides results in arsenic accumulation in water. In contrast, the surface-mediated oxidation of FeS at basic pH leads to the direct formation of Fe (oxyhydr)oxides, which provides effective adsorbents for As under oxic conditions. At acidic and neutral pH, the solution-phase oxidation of dissolved Fe(II) accelerates the oxidation of the less adsorbing As(III) to the more adsorbing As(V). This study reveals that the oxidative mobilization of As may be a significant pathway for arsenic enrichment of porewaters in sulfidic sediments.