聚铁改性絮凝剂的合成与水处理试验

研究了一种通过用聚铁改性来制备聚硅酸硫酸铁的方法,考察了改性剂中的SiO2质量分数、铁硅比、活化时间、pH值等参数对PFSS(聚硅酸硫酸铁)性能的影响,并进行了水处理实验.结果表明,PFSS制备适宜参数条件为SiO2质量分数为2.0%、铁硅比10:1、活化时间4.Oh,此时其对原水中的浊度和高锰酸盐指数去除率可分别达到98.4%～72.4%,处理后的原水达到饮用水的水质要求.     

Tidal variability in benthic silicic acid fluxes and microphytobenthos uptake in intertidal sediment

Silicic acid (DSi) benthic fluxes play a major role in the benthic–pelagic coupling of coastal ecosystems. They can sustain microphytobenthos (MPB) development at the water–sediment interface and support pelagic diatoms when river DSi inputs decrease. DSi benthic fluxes have been studied at the seasonal scale but little is known about their dial variations. This study measured the amplitude of such variations in an intertidal area over an entire tidal cycle by following the alteration of DSi pore water concentrations at regular intervals over the flood/ebb period. Furthermore we independently estimated the potential DSi uptake by benthic diatoms and compared it to the variations of DSi pore water concentrations and fluxes. The microphytobenthos DSi demand was estimated from primary production measurements on cells extracted from the sediment. There were large changes in DSi pore water concentration and a prominent effect of tidal pumping: the DSi flushed out from the sediment at rising tide, occurs in a very short period of time, but plays a far more important role in fueling the ecosystem (800 μmol-Si m⁻² d⁻¹), than diffusive fluxes occurring throughout the rest of the tidal cycle (2 μmol-Si m⁻² d⁻¹). This process is not, to our knowledge, currently considered when describing the DSi cycling of intertidal sediments. Moreover, there was a large potential MPB requirement for DSi (812 μmol-Si m⁻² d⁻¹), similar to the advective flow periodically pumped by the incoming tide, and largely exceeded benthic diffusive fluxes. However, this DSi uptake by benthic diatoms is almost undetectable given the variation of DSi concentration profiles within the sediment.     

Tephra dispersal from Myojinsho, Japan, during its shallow submarine eruption of 1952–1953

 A new and detailed bathymetric map of the Myojinsho shallow submarine volcano provides a framework to interpret the physical volcanology of its 1952–1953 eruption, especially how the silicic pyroclasts, both primary and reworked, enlarged the volcano and were dispersed into the surrounding marine environment. Myojinsho, 420 km south of Tokyo along the Izu–Ogasawara arc, was the site of approximately 1000 phreatomagmatic explosions during the 12.5-month eruption. These explosions shattered growing dacite domes, producing dense clasts that immediately sank into the sea; minor amounts of pumice floated on the sea surface after some of these events. The Myojinsho cone has slopes of almost precisely 21° in the depth range 300–700 m.We interpret this to be the result of angle-of-repose deposition of submarine pyroclastic gravity flows that traveled downslope in all directions. Many of these gravity flows resulted from explosions and associated dome collapse, but others were likely triggered by the remobilization of debris temporarily deposited on the summit and steep upper slopes of the cone. Tephra was repeatedly carried into air in subaerial eruption columns and fell into the sea within 1–2 km of the volcano's summit, entering water as deep as 400 m. Because the fall velocity of single particles decreased by a factor of ∼30 in passing from air into the sea, we expect that the upper part of the water column was repeatedly choked with hyperconcentrations of fallout tephra. Gravitational instabilities within these tephra-choked regions could have formed vertical density currents that descended at velocities greater than those of the individual particles they contained. Upon reaching the sea floor, many of these currents probably continued to move downslope along Myojinsho's submarine slopes. Fine tephra was elutriated from the rubbly summit of the volcano by upwelling plumes of heated seawater that persisted for the entire duration of the eruption. Ocean currents carried this tephra to distal areas, where it presumably forms a pyroclastic component of deep-sea sediment. Received: 5 December 1996 / Accepted: 17 September 1997     

Desilication veins in the Cadillac Mountain granite (Maine, USA): a record of reversals in the SiO2 solubility of H2O-rich vapour released during subsolidus cooling

Late-stage hydrous fluids, which evolved during the cooling of the Cadillac Mountain granite, Maine, USA, produced narrow veins that transect the pluton. The vein margins contain microstructures transitional between granite and the vein centre. They preserve the vestige shapes of original Na-rich alkali feldspar crystals that have been pseudomorphed by cordierite+quartz+K-rich alkali feldspar. Closer to the centres of the veins, the minerals change from an outer zone with cordierite, hercynitic–galaxite spinel, minor corundum, K-feldspar and plagioclase to an inner zone with remnant cordierite, hercynitic gahnite, strongly zoned almandine–spessartine garnet, chlorite and quartz. Three allochemical reactions are inferred to have occurred with the influx of hydrous fluids during the replacement process. Reaction (1) is Na-rich alkali feldspar+iron ions in solution=Fe-cordierite+quartz+K-feldspar+sodium ions in solution. Reactions (2) and (3) occurred during desilication. Reaction (2) is Fe-cordierite=hercynite+silica in solution, and reaction (3) is Fe-cordierite+water=corundum+iron hydroxide in solution+silicic acid in solution. Two independent techniques, experimental silica-solubility data and spinel–cordierite thermobarometry, constrain the conditions of vein formation to c.   1.0  kbar and both methods indicate that the progressive mineral reactions occurred during cooling of the hydrous fluids from c. 775° to 400–340  °C. This cooling trend is consistent with the petrographic evidence, which demonstrates that reactions occurred before desilication, during desilication, and then diminished with a final phase of resilication. Although the veins are minor features of the Cadillac Mountain granite, they provide insight into the conditions that prevailed during cooling of the pluton, and similar features may be important for constraining the cooling history of shallow-level plutonic complexes elsewhere.     

Textures, water content and degassing of silicic andesites from recent plinian and dome-forming eruptions at Mount Pelée volcano (Martinique, Lesser Antilles arc)

Previous petrological and phase-equilibrium experimental studies on recent silicic andesites from Mount Pelée volcano have evidenced comparable pre-eruptive conditions for plinian and dome-forming (pelean herein) eruptions, implying that differences in eruptive style must be primarily controlled by differences in degassing behaviour of the Mount Pelée magmas during eruption. To further investigate the degassing conditions of plinian and pelean magmas of Mount Pelée, we study here the most recent Mount Pelée's products (P1 at 650 years B.P., 1902, and 1929 eruptions, which cover a range of plinian and pelean lithologies) for bulk-rock vesicularities, glass water contents (glass inclusions in phenocrysts and matrix glasses) and microtextures. Water contents of glass inclusions are scattered in the plinian pumices but on average compare with the experimentally-deduced pre-eruptive melt water content (i.e., 5.3–6.3 wt.%), whereas they are much lower in the dominant pelean lithologies (crystalline, poorly vesicular lithics and dome samples). This indicates that the glass inclusions of the pelean products have undergone strong leakage and do not represent pre-eruptive water contents. The water content of the pyroclast matrix glasses are thought to closely represent the residual water content in the melt at the time of fragmentation. Determination of the water contents of both the pre-eruptive melt and matrix glasses allows the estimation of the amount of water exsolved upon syn-eruptive degassing. We find the amount of water exsolved during the eruptive process to be higher in the pelean products than in the plinian ones, typically 90–100 and 65–70% of the initial water content, respectively. The vesicularities calculated from the amount of exsolved water compare with the measured vesicularities for the plinian pumices, consistent with a closed-system, near-equilibrium degassing up to fragmentation. By contrast, the low residual water contents, low groundmass vesicularities and extensive groundmass crystallization of the pelean products are direct evidence of open-system degassing. Microtextural features, including silica-bearing and silica-free voids in the pelean lithologies may represent a two-stage vesiculation.     

Early to middle Holocene silicic tephra horizons from the Katla volcanic system,Iceland: new results from the Faroe Islands

Comparatively few Icelandic tephra horizons dated to the early part of the Holocene have so far been detected outside Iceland. Here, I present several tephra horizons that have been recorded in a Holocene peat sequence on the Faroe Islands. Geochemical analyses show that at least two dacitic and one rhyolitic tephra layers were erupted from the Katla volcanic system on southern Iceland between ca. 8000 and 5900 cal. yr BP. The upper two layers can be correlated with the SILK tephras described from southern Iceland, whereas the third, dated to ca. 8000 cal. yr BP, has a geochemistry virtually identical to the rhyolitic component of the Vedde Ash. The results suggest that the Late Weichselian and early Holocene eruption history of the Katla volcano was probably more complex than inferred from Iceland. A new, early Holocene rhyolitic tephra dated to ca. 10 500 cal. yr BP probably originates in the Snæfellsnes volcanic centre in western Iceland. These new findings may play an important role in developing a Holocene tephra framework for northwest Europe. Copyright © 2002 John Wiley & Sons, Ltd.     

Effects of relative motion between gas and liquid on 1-dimensional steady flow in silicic volcanic conduits: 2. Origin of diversity of eruption styles

We investigate the origin of diversity of eruption styles in silicic volcanoes on the basis of a 1-dimensional steady conduit flow model that considers vertical relative motion between gas and liquid (i.e., vertical gas escape). The relationship between the assemblage of steady-state solutions in the conduit flow model and magma properties or geological conditions is expressed by a regime map in the parameter space of the ratio of liquid-wall friction force to liquid–gas interaction force (non-dimensional number ε), and a normalized conduit length Λ. The regime map developed in the companion paper shows that when ε is smaller than a critical value ε_cr, a solution of explosive eruption exists for a wide range of Λ, whereas an effusive solution exists only when Λ ~ 1. On the other hand, when ε > ε_cr, an effusive solution exists for a wide range of Λ. Diversity of eruption styles observed in nature is explained by the change in ε accompanied by the change in magma viscosity during magma ascent. As magma ascends, the magma viscosity increases because of gas exsolution and crystallization, leading to the increase in ε. For the viscosity of hydrous silicic magma at magma chamber, ε is estimated to be smaller than ε_cr, indicating that an explosive solution exists for wide ranges of geological parameters. When magma flow rate is small, the viscosity of silicic magma drastically increases because of extensive crystallization at a shallow level in the conduit. In this case, ε can be greater than ε_cr; as a result, a stable effusive solution co-exists with an explosive solution.     

原子荧光法测定高纯石墨粉中的砷、锑

提出以硫脲-抗坏血酸-硼氢化钾反应体系,利用氢化物发生原子荧光法测定高纯石墨粉中的砷、锑含量。讨论了试剂纯度的影响、硫脲一抗坏血酸预还原时间的选择、干扰试验、硼氢化钾溶液的用量等影响。实验结果表明,该方法对高纯石墨粉中的砷、锑含量分析准确、快速、简便,在试验条件下,砷的检出限为0．02mg／kg、锑的检出限为0．007mg／kg;砷的回收率为94％～108％、锑的回收率为96％～108％。采用该方法能满足电池行业用石墨规定的指标。     

Experimental and Thermodynamic Constraints on the Sulphur Yield of Peralkaline and Metaluminous Silicic Flood Eruptions

Many basaltic flood provinces are characterized by the existenceof voluminous amounts of silicic magmas, yet the role of thesilicic component in sulphur emissions associated with trapactivity remains poorly known. We have performed experimentsand theoretical calculations to address this issue. The meltsulphur content and fluid/melt partitioning at saturation witheither sulphide or sulphate or both have been experimentallydetermined in three peralkaline rhyolites, which are a majorcomponent of some flood provinces. Experiments were performedat 150 MPa, 800–900°C, fO₂ in the range NNO –2 to NNO + 3 and under water-rich conditions. The sulphur contentis strongly dependent on the peralkalinity of the melt, in additionto fO₂, and reaches 1000 ppm at NNO + 1 in the most stronglyperalkaline composition at 800°C. At all values of fO₂,peralkaline melts can carry 5–20 times more sulphur thantheir metaluminous equivalents. Mildly peralkaline compositionsshow little variation in fluid/melt sulphur partitioning withchanging fO₂ (D_S 270). In the most peralkaline melt, D_S risessharply at fO₂ > NNO + 1 to values of >500. The partitioncoefficient increases steadily for S_bulk between 1 and 6 wt% but remains about constant for S_bulk between 0·5 and1 wt %. At bulk sulphur contents lower than 4 wt %, a temperatureincrease from 800 to 900°C decreases D_S by 10%. These results,along with (1) thermodynamic calculations on the behaviour ofsulphur during the crystallization of basalt and partial meltingof the crust and (2) recent experimental constraints on sulphursolubility in metaluminous rhyolites, show that basalt fractionationcan produce rhyolitic magmas having much more sulphur than rhyolitesderived from crustal anatexis. In particular, hot and dry metaluminoussilicic magmas produced by melting of dehydrated lower crustare virtually devoid of sulphur. In contrast, peralkaline rhyolitesformed by crystal fractionation of alkali basalt can concentrateup to 90% of the original sulphur content of the parental magmas,especially when the basalt is CO₂-rich. On this basis, we estimatethe amounts of sulphur potentially released to the atmosphereby the silicic component of flood eruptive sequences. The peralkalineEthiopian and Deccan rhyolites could have produced 10¹⁷ and10¹⁸ g of S, respectively, which are comparable amounts to publishedestimates for the basaltic activity of each province. In contrast,despite similar erupted volumes, the metaluminous Paraná–Etendekasilicic eruptives could have injected only 4·6 x 10¹⁵g of S in the atmosphere. Peralkaline flood sequences may thushave greater environmental effects than those of metaluminousaffinity, in agreement with evidence available from mass extinctionsand oceanic anoxic events. KEY WORDS: silicic flood eruptions; sulphur; experiment; Ethiopia; Deccan     

Presence of native gold and tellurium in the active high-sulfidation hydrothermal system of the La Fossa volcano (Vulcano, Italy)

Grains of native gold and tellurium were found in siliceous hydrothermally altered rocks in the high-temperature (170–540°C) fumarolic field of the La Fossa volcano (Island of Vulcano). In addition to Au and Te, Pb–Bi sulfides (cannizzarite) and Tl-bromide chloride were found as sublimates in the hottest fumarolic vents of the crater rim. The chemical composition of altered rocks associated with sublimate deposition indicate the presence of a significant concentration of Te (up to 75 ppm), while gold concentrations are very low (<9 ppb). Pb, Bi and Tl are strongly enriched in the hottest and less oxidized fumarolic vents, reaching concentrations of 2186, 146 and 282 ppm, respectively. These elements are transported (generally as chloride complexes) to the surface by volcanic gases, and several of these (Bi, Te, Tl) are originated from magma degassing. The silicic alteration is produced by the flow of fluids with pH<2. High acidity results from introduction of magmatic gases such as SO₂, HCl and HF released by the shallow magmatic reservoir of La Fossa volcano. The silicic alteration found at Vulcano may represent an early stage of the `vuggy silica' facies which characterizes the high-sulfidation epithermal ore deposits, confirming the analogies existing between this type of ore deposit and magmatic-hydrothermal systems associated with island-arc volcanoes.