Thaumasite––direct, woodfordite and other possible formation routes

Two main formation routes for thaumasite exist below 15 °C. One is the direct route from C–S–H reacting with appropriate carbonate, sulfate, Ca²⁺ ions and excess water. The other route is the woodfordite route from ettringite reacting with C–S–H, carbonate, Ca²⁺ ions and excess water, in which thaumasite arises through the intermediate formation of the solid solution woodfordite. The woodfordite route for thaumasite formation appears to be relatively quicker (although still slow) than the direct route, presumably because with the former the ettringite already has the octahedral [M(OH)₆] units that can facilitate the critical change from [Al(OH)₆]³⁻ to [Si(OH)₆]²⁻ groupings. Both routes are mutually dependent on each other. The presence of magnesium salts can modify the path to thaumasite formation. High pressure might be able to stabilise [Si(OH)₆]²⁻ groupings and allow thaumasite to become formed above 15 °C. This possibility is discussed.     

由AEO_3硫酸化合成AES的研究

以氨基磺酸和氯磺酸作硫酸化剂,由AEO_3合成了AES,讨论了工艺条件对反应过程和产品质量的影响。     

流动微量量热法研究阴离子表面活性剂在油砂表面的吸附

用流动微量量热法研究了十二烷基硫酸钠(SDDS)和十二碳羧酸钠(SL)在克拉玛依油田九区和乌尔禾区油砂上的吸附,简要地计论了吸附机理。所得实验结果表明,SL 在油砂上的吸附强度比 SDDS 的要大,在相当低的浓度下即可迟到饱和吸附。     

The effect of liquid push out of the material capillaries under sulfate ion diffusion in cement composites

The paper treats complex phenomena that accompany the diffusion of sulfate ions into cement paste or systems. The ion distribution within the material was studied by designing a specific diffusion model. The model accounts for two phenomena: capillary filling with products of the chemical reactions and the subsequent liquid push out of the capillary. The approach allows to quantify the concentration of free ions having penetrated the cement stone and that of chemically reacted ions, and to assess the liquid push out. Experimental data are also presented.     

一种新型硫酸亚铁单液法调剖剂

本文提出用尿素作为ｐⅡ调节剂，加快硫酸亚铁单液法调剖剂中亚铁离子在地层温度下的沉淀，增大沉淀率，提高封堵效能。岩芯流动试验结果表明，１５％ＦｅＳＯ４．７ＩＩ ２Ｏ／５％尿素调剖剂体系的封堵能力比不含尿素的体系增大近一倍。     

Effect of sulfate on Cu(Ⅱ) sorption to polymer-supported nano-hydrated ferric oxides: Experimental and modeling studies

Incorporating of hydrous ferric oxide(HFO) inside porous supports with large sizes has become an effective way to decontaminate the water from heavy metals. Ubiquitous anions like sulfate are usually present in high concentrations in water, and might greatly affect adsorption behavior of hybrid HFO. Here, a polymer-based HFO-CPS was fabricated by encapsulating nano-HFO inside a chloromethylated polystyrene polymer(CPS) and the reactivity of HFO-CPS with Cu(Ⅱ) was evaluated in the presence of sulfate ions.Surface complexation theory was firstly employed to describe the effect of sulfate on Cu(Ⅱ) adsorption edges of hybrid HFO-CPS, where constant capacitance model(CCM) was adopted. The available weak adsorption site Fe_((2))OH of hybrid HFO-CPS was found to decrease from 20% Fe to 5% Fe, which might be caused by the pore plugging effect after HFO encapsulation. With the assumption that a ternary complex was formed, the effect of sulfate on Cu(Ⅱ) adsorption by HFO-CPS were successfully described by CCM using the optimized Fe_((2))OH site under different sulfate concentrations(1 or 10 mmol·L~(-1)) and Cu/Fe ratios(0.0042 or 0.0252). It is confirmed that the formation of Fe OHCu SO_4 ternary surface complexes played an important role in enhancing Cu(Ⅱ) adsorption on HFO-CPS in the presence of sulfate.     

Stability of protective oxide films in waste incineration environment—solubility measurement of oxides in molten chlorides

Solubility measurements of several oxides in molten NaCl-KCl and NaCl-KCl-Na₂SO₄-K₂SO₄ were conducted in three different levels of basicity. The dissolution behavior of the oxides showed almost the same tendency as that shown by the dissolution behavior of the oxides in molten Na₂SO₄ in literature. In a waste incineration environment, a protective Cr₂O₃ film easily dissolves in molten chlorides as CrO₄²⁻ because pO²⁻ of the molten chlorides tends to have a small value due to the effect of water vapor contained in the combustion gas. From the result of the solubility measurement, the addition of molybdenum and/or silicon was expected to improve the corrosion resistance of alloys. Laboratory corrosion tests confirmed this expectation. However, the scale analysis suggested that the effect of molybdenum could not be explained completely by only the mechanism derived from the result of the solubility measurement.     

季鏻盐型缓蚀剂对SRB诱导碳钢腐蚀过程的缓蚀与杀菌作用

采用最大可能计数法对两种季盐型缓蚀剂BHP 1及BHP 2的杀菌效果进行了评价。结果发现 ,BHP 1具有良好的杀菌性能 ,且最佳杀菌浓度为 6 0× 10 -6g/L ,两者的杀菌效果均优于广泛使用的新洁尔灭。采用电化学方法、腐蚀失重实验及表面分析法研究了 4 5 # 碳钢在含硫酸盐还原菌 (SRB)的厌氧体系中的腐蚀行为。结果表明 :SRB能加速 4 5 # 碳钢的点蚀破坏。两种季盐能有效控制SRB溶液对 4 5 # 碳钢的腐蚀破坏 ,使点蚀电位正移 ,对SRB溶液中的 4 5 # 碳钢具有良好的缓蚀作用 ,缓蚀效果为BHP 1>BHP 2     

Long-term performance of cement paste during combined calcium leaching-sulfate attack: kinetics and size effect

This paper presents experimental results obtained on cement paste samples (water/cement ratio of 0.4) subjected to a low-concentration (15 mmol/l) external sulfate attack during several weeks. Chemical and microstructural analyses include the continuous monitoring of calcium loss and sulfate consumption within the cement paste, periodic layer by layer X-ray diffraction (XRD)/energy-dispersive spectrometer (EDS) analyses of the solid constituents of the cement matrix (ettringite, portlandite, gypsum) within the calcium-depleted part of the samples. Scanning electron microscopy (SEM) and visual observations are used to follow the crack pattern evolution during the external sulfate attack. The relation between the size of the specimen and crack initiation/development is investigated experimentally by performing tests on samples with different thickness/diameter ratios.     

Tetragonal structure, anionic vacancies and catalytic activity of SO4-ZrO2 catalysts for n-butane isomerization

An assessment of the influence of the crystal structure, surface hydroxylation state and previous oxidation/reduction pretreatments on the activity of sulfate-zirconia catalysts for isomerization of n-butane was performed using crystalline and amorphous zirconia supports. Different sulfation methods were used for the preparation of bulk and supported SO₄²⁻-ZrO₂ with monoclinic, tetragonal and tetragonal+monoclinic structures. Activity was important only for the samples that contained tetragonal crystals. The catalysts prepared from pure monoclinic zirconia showed negligible activity. SO₄²⁻-ZrO₂ catalysts prepared by sulfation of crystalline zirconia displayed sites with lower acidity and cracking activity than those sulfated in the amorphous state. Prereduction of the zirconia samples with H₂ was found to greatly increase the catalytic activity, and a maximum rate was found at a reduction temperature of 550–600 °C, coinciding with a TPR peak supposedly associated with the removal of lattice oxygen and the creation of lattice defects. A weaker dependence of catalytic activity on the density or type of surface OH groups on zirconia (before sulfation) was found in this work.

A model of active site generation was constructed in order to stress the dependence on the crystal structure and crystal defects. Current and previous results suggest that tetragonal structure in active SO₄²⁻-ZrO₂ is a consequence of the stabilization of anionic vacancies in zirconia. Anionic vacancies are in turn supposed to be related to the catalytic activity for n-butane isomerization through the stabilization of electrons from ionized intermediates.