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磷矿酸不溶残渣对α-半水石膏水化过程及力学性能的影响

Effect of phosphate rock acid insoluble residue on hydration process and mechanical properties of α-hemihydrate gypsum.

作者信息

Wang Yu, Zhang Yu, He Weilong, Nie Dengpan

机构信息

School of Chemistry and Chemical Engineering, Guizhou University, Guizhou, Guiyang, 550025, People's Republic of China.

School of Chemical Engineering, Guizhou Minzu University, Guizhou, Guiyang, 550025, People's Republic of China.

出版信息

Environ Sci Pollut Res Int. 2023 May;30(22):62815-62831. doi: 10.1007/s11356-023-26484-6. Epub 2023 Mar 22.

Abstract

The application of α-hemihydrate gypsum (α-HH) is limited by several factors, such as a rapid hydration rate, short setting time, poor water resistance, and high cost. Especially because of the high production cost, although α-HH has excellent mechanical strength, it is rarely used in the field of building materials. In this study, based on the composition characteristics of new industrial solid waste (phosphate-rock acid-insoluble residue, PAIR) and to meet the needs of resource utilization, gypsum matrix composites were prepared by adding PAIR to α-HH to solve the problems of short setting time and poor water resistance of gypsum matrix composites and improve the comprehensive properties of α-HH products. The results show that when the different types of pores formed during the hydration of α-HH were filled with inert substances, such as silicon dioxide, insoluble phosphate, and calcium fluoride from PAIR, the proportion of mesopores in the composite products increased, whereas that of harmful macropores decreased. The compressive and flexural softening coefficients of the PAIR/α-HH system with 23% PAIR were the highest at 57.25 and 60.125%, respectively, and the water resistance of the system was improved; when the content of PAIR reaches 35%, the strength of the composite products decreased from 58.125 to 43.8 MPa. The HPO in PAIR partially replaces the SO ion in the dihydrate gypsum (DH) lattice to form a Ca(SO, HPO)•2HO double salt, leading to the production of eutectic phosphorus. Soluble F, Al, Mg, and phosphorus-containing substances in PAIR form a variety of complex ions in PAIR/α-HH aqueous solution, which are adsorbed onto the surface of the new DH phase; the crystal morphology changed from thick, long columns to clusters, thin rods, and plates, inhibiting the nucleation and growth of DH and changing its crystal growth rate and crystallization behavior. Therefore, the setting time of gypsum is prolonged; when 35% PAIR was added, the induced nucleation period of the PAIR/α-HH system was prolonged from 40 to 265 min, and the final setting time was from 12 to 360 min. By mixing solid waste PAIR, while the setting time of α-HH is prolonged, its water resistance is improved, and its mechanical strength is not significantly reduced, reducing the cost. From the perspective of economy and environmental protection, this study is a way to α-HH is widely used in the field of building materials.

摘要

α-半水石膏(α-HH)的应用受到多种因素的限制,如水化速率快、凝结时间短、耐水性差和成本高。特别是由于生产成本高,尽管α-HH具有优异的机械强度,但在建筑材料领域很少使用。在本研究中,基于新型工业固体废弃物(磷矿酸不溶残渣,PAIR)的组成特性,并为满足资源利用的需求,通过向α-HH中添加PAIR制备石膏基复合材料,以解决石膏基复合材料凝结时间短和耐水性差的问题,并提高α-HH产品的综合性能。结果表明,当α-HH水化过程中形成的不同类型孔隙被PAIR中的二氧化硅、不溶性磷酸盐和氟化钙等惰性物质填充时,复合材料产品中中孔比例增加,有害大孔比例降低。PAIR含量为23%的PAIR/α-HH体系的抗压和抗折软化系数分别最高,为57.25%和60.125%,体系的耐水性得到改善;当PAIR含量达到35%时,复合材料产品的强度从58.125MPa降至43.8MPa。PAIR中的HPO部分取代二水石膏(DH)晶格中的SO离子,形成Ca(SO, HPO)•2HO复盐,导致共晶磷的产生。PAIR中的可溶性F、Al、Mg和含磷物质在PAIR/α-HH水溶液中形成多种络合离子,吸附在新形成的DH相表面;晶体形态从粗长柱状变为簇状、细棒状和平板状,抑制了DH的成核和生长,改变了其晶体生长速率和结晶行为。因此,石膏的凝结时间延长;当添加35%PAIR时,PAIR/α-HH体系的诱导成核期从40分钟延长至265分钟,终凝时间从12分钟延长至360分钟。通过混合固体废弃物PAIR,在延长α-HH凝结时间的同时,提高了其耐水性,且其机械强度没有显著降低,降低了成本。从经济和环保角度来看,本研究是一种使α-HH在建筑材料领域广泛应用的方法。

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