首页> 外文期刊>Journal of Environmental Engineering >XRD and Unconfined Compressive Strength Study for a Qualitative Examination of Calcium–Arsenic Compounds Retardation of Cement Hydration in Solidified/Stabilized Arsenic–Iron Hydroxide Sludge
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XRD and Unconfined Compressive Strength Study for a Qualitative Examination of Calcium–Arsenic Compounds Retardation of Cement Hydration in Solidified/Stabilized Arsenic–Iron Hydroxide Sludge

机译:XRD和无侧限抗压强度研究对定性/稳定化的砷化铁氢氧化物污泥中水泥水合的钙-砷化合物的定性检测

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This study investigates the adverse effects of synthesized arsenic–iron hydroxide sludge, the by-product of arsenic removal by coagulation with ferric chloride, on unconfined compressive strength (UCS) and cement hydration of solidified/stabilized matrices. The results from both UCS tests and X-ray diffraction (XRD) implied that synthesized arsenic–iron hydroxide sludge might not be chemically inert in a cementitious environment, which could account for the retardation of cement hydration. The culprit for this retardation is likely to be the multiphase formation of calcium arsenic compounds suggested by the strong peak at 7.90 ? (11.2° 2). This peak appeared when more than 20 and 13% of arsenic–iron hydroxide sludge were added to the solidification/stabilization (S/S) process of cement–water and cement-hydrated lime–water systems, respectively. The proposed mechanisms for the retardation of cement hydration by calcium–arsenic compounds are calcium complexation and, subsequently, surface precipitation due to the interaction between desorbed arsenate and hydration by-products in a cement porewater environment. The extent of the hydration retardation is qualitatively determined by the semiquantitative comparison of Ca3SiO5 and Ca2SiO4 remaining after 28 days of hydration between the control S/S samples and that with various doses of the sludge added. When 20 and 33% of the sludge were added into the S/S matrices, the remaining Ca3SiO5 and Ca2SiO4 were more than that of the control sample by factors of 2 and 3.2, respectively.
机译:这项研究调查了合成的砷铁氢氧化物污泥,通过氯化铁凝结去除砷的副产物对无侧限抗压强度(UCS)和固化/稳定基质的水泥水化的不利影响。 UCS测试和X射线衍射(XRD)的结果均表明,合成的砷铁氢氧化物污泥在胶结环境中可能不是化学惰性的,这可能是造成水泥水化延迟的原因。这种延迟的罪魁祸首很可能是砷酸钙化合物的多相形成,这是由于在7.90?处的强峰所致。 (11.2°2)。当分别向水泥-水系统和水泥-水合石灰-水系统的固化/稳定化(S / S)过程中添加了20%和13%以上的砷-氢氧化铁污泥时,就会出现该峰。钙-砷化合物对水泥水化的阻滞机理是钙络合,以及由于水泥孔隙水环境中解吸的砷酸盐和水合副产物之间的相互作用而引起的表面沉淀。水合延迟的程度通过对照S / S样品与添加了不同剂量污泥的水合28天后残留的Ca3SiO5和Ca2SiO4的半定量比较来定性确定。当将20%和33%的污泥添加到S / S基质中时,剩余的Ca3SiO5和Ca2SiO4分别比对照样品多2倍和3.2倍。

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