冶金渣制备高强人工鱼礁结构材料的试验研究

为了研究钢渣粉磨时间和矿渣钢渣复掺比例对矿渣-钢渣-熟料-石膏体系胶凝材料强度的影响,采用一次线性回归得到胶凝材料强度的变化趋势,并利用XRD和SEM方法分析钢渣粉磨和净浆的水化过程.试验表明:矿渣与钢渣的复合比为7∶1,钢渣和矿渣的比表面积分别为550和480 m2/kg,且与质量分数10%的水泥熟料和质量分数10%的脱硫石膏复合的胶凝材料具有较高的强度.以优化后的胶凝材料代替水泥,并以热闷法稳定化的钢渣颗粒为骨料,可以制备出抗压强度达到60 MPa以上,水泥熟料总用量为2%的高强人工鱼礁混凝土.研究表明,对钢渣适度粉磨能改善钢渣性能,适量加入钢渣对促进体系的水化有积极作用.     

钢渣粉性能优化及制备无熟料混凝土的试验研究

为提高固体废弃物综合利用率,通过钢渣分段除铁优化试验和钢渣粉对无熟料混凝土抗压强度影响试验,研究以钢渣-矿渣-脱硫石膏作为胶凝材料制备无熟料全固废混凝土。结果表明,经分段磁选可获得金属铁含量低于0.5%的高性能钢渣粉;当钢渣粉比表面积为640m~2/kg,m(钢渣)∶m(矿渣)=1∶2.5时,无熟料混凝土同时获得较优的3d和28d强度。XRD、TG-DSC、IR和FE-SEM分析表明,在脱硫石膏的激发作用下钢渣和矿渣可以相互促进水化,水化产物以AFt(钙矾石)和C-S-H(水化硅酸钙)凝胶为主。早期钢渣水化促进矿渣的解聚并结合脱硫石膏生成AFt网状结构,随着水化反应的进行胶凝体系生成的C-S-H凝胶充填于AFt网络中使硬化浆体结构致密从而保证强度的增长。     

钢渣激发脱硫石膏水硬性胶凝材料的研究

研究旨在开发一种以钢渣为碱性激发剂,以烟气脱硫石膏、矿渣粉为主要为原料的脱硫石膏水硬性胶凝材料。该胶凝体系3天抗折强度和抗压强度可达4.4 MPa和15.8 MPa;28天抗折强度和抗压强度可达9.4 MPa和50.7 MPa。其试样的强度随钢渣掺量的增加而增加,而钢渣含量一旦超过8%后,增长幅度变缓,甚至开始降低。XRD和SEM分析表明,脱硫石膏-矿渣-激发剂体系的水化产物主要是钙矾石和C-S-H凝胶。脱硫石膏在水化过程中一部分参与水化形成水化产物钙矾石,其余部分被水化产物所包裹起集料骨架作用。     

钢渣矿渣基全固废胶凝材料的水化反应机理

以钢渣、矿渣和脱硫石膏为主要原料制备胶凝材料,使用XRD、IR、TG-DTA和SEM等手段探究胶凝材料的水化反应机理,研究了钢渣掺量对全固废混凝土强度的影响,以及胶凝材料浆体的p H值和代表性离子浓度的变化规律。结果表明,当原料质量比为m(钢渣):m(矿渣):m(石膏)=30:58:12时,全固废混凝土3 d、7 d和28 d可以获得较优的强度。随着反应龄期的增加胶凝材料水化溶液的pH值先减小后增大,Ca2+浓度和硅(铝)溶解物的早期浓度较低,后期浓度有所提高。在脱硫石膏的激发下钢渣和矿渣相互促进水化,水化产物以钙矾石(AFt)和水化硅酸钙(C-S-H)凝胶为主。在反应的后期,水化产物的数量迅速增加。针棒状的AFt晶体穿插在C-S-H凝胶内,使硬化浆体的结构更加致密。     

粉煤灰基固废胶凝材料流变特性机理研究

为研究适用于高浓度废弃尾矿砂浆充填体的胶凝材料，通过扩展度等试验检测不同粉煤灰掺量下砂浆流变特性，并分析试验方法的适用性；通过检测砂浆微观性质探究粉煤灰基胶凝材料作用机理。结果表明：扩展度与L管模型试验的相关性为0.985,说明扩展度可作为L管的预试验，协同表征砂浆流变性能；掺入10%粉煤灰的砂浆屈服应力降低了13.06%～24.74%,3 d强度提升了40%,7 d强度提升了9.9%,使固废综效得以充分发挥；随粉煤灰含量逐渐增加，浆液离子浓度逐渐降低，导致胶凝颗粒间斥力增加，颗粒更为分散；同时10%掺量粉煤灰的浆液3 d水化放热累计量261.696 J/g,提升了2.9%,孔隙率15.15%降低了4.02%,即粉煤灰的“滚珠”特性一定程度上改善了流动性并提升了硬化体强度。     

钢渣激发脱硫石膏水硬性胶凝材料的研究

研究旨在开发一种以钢渣为碱性激发剂,以烟气脱硫石膏、矿渣粉为主要为原料的脱硫石膏水硬性胶凝材料。该胶凝体系3天抗折强度和抗压强度可达4.4 MPa和15.8 MPa;28天抗折强度和抗压强度可达9.4 MPa和50.7 MPa。其试样的强度随钢渣掺量的增加而增加,而钢渣含量一旦超过8%后,增长幅度变缓,甚至开始降低。XRD和SEM分析表明,脱硫石膏-矿渣-激发剂体系的水化产物主要是钙矾石和C-S-H凝胶。脱硫石膏在水化过程中一部分参与水化形成水化产物钙矾石,其余部分被水化产物所包裹起集料骨架作用。     

掺石膏的低钙水泥水化过程及浆体结构研究

利用高铝粉煤灰可烧制主要矿物组成为硫铝酸钙■和硅酸二钙的低钙水泥(LCC),石膏■对■系列胶凝材料的水化性能起重要作用。为推广LCC的应用,研究了不同■掺量的LCC水化性能。通过等温量热仪、扫描电子显微镜、压汞仪等分析了LCC水化过程及浆体结构,并对LCC抗压强度进行检测。结果表明,随着■掺量增加,LCC水化反应加速,产物钙矾石(AFt)增多且由针状向柱状演变,浆体孔隙率呈现下降趋势;少量■(1%(质量分数))有利于浆体中水化钙铝黄长石的形成,28 d强度增长22.6%;■掺量为5%时,各龄期强度均显著提升;■掺量较高时(10%),浆体早期性能发展迅速而后期性能未见改善;过量■促使AFt发育成管、柱状,尽管浆体孔隙率降至8.4%,但形成了较多微米级粗孔,不利于后期性能提升;不同■掺量(1%～20%)的LCC强度均稳定发展且后期强度不倒缩,展现了LCC的广阔应用前景。     

大掺量工业废渣激发制备钢渣复合胶凝材料的试验研究

在研究不同钢渣掺量胶凝体系稳定性的基础上,以40%的钢渣粉掺加15%矿渣粉、5%硅灰粉,采用自配复合激发剂成功地制备出早期抗折强度、抗压强度达到4.5MPa、18.8MPa且满足42.5强度等级的复合胶凝材料,通过其孔隙率及微观结构测试分析表明:钢渣复合胶凝材料水化产物致密,孔隙率低,后期抗压强度、抗折强度发展较好。     

早龄期复合胶凝材料的裂纹扩展阻力分析

研究了不同组成的复合胶凝材料硬化浆体(硅酸盐水泥,硅酸盐水泥 粉煤灰,硅酸盐水泥 矿渣,硅酸盐水泥 硅灰,硅酸盐水泥 硅灰 粉煤灰)早龄期时裂纹扩展阻力的发展,探讨了粉煤灰掺量对裂纹扩展阻力的影响.结果表明:早龄期时,在相同水胶比条件下,掺加硅灰使胶凝材料体系裂纹扩展阻力明显降低,在低水胶比条件下,掺加一定量的粉煤灰能够明显增加体系的裂纹扩展阻力,掺加20%的粉煤灰能使胶凝材料具有较高的裂纹扩展阻力.     

超细矿渣粉对硅酸盐水泥性能和微观结构的影响

通过掺入不同量的超细矿渣粉,研究其对普通硅酸盐水泥凝结时间、标准稠度用水量以及水泥胶砂流动性和强度的影响。结果表明,水泥浆体的初凝、终凝时间在矿渣粉掺量为5%(质量分数,下同)时有所缩短,而随着超细矿渣粉掺量的增加,初凝时间都有所延长,在掺量为20%时初凝时间最长。然而终凝时间的变化不大,只有掺量为30%时稍有延长;水泥的标准稠度用水量先减少后增加,在掺量为20%时最小;随着超细矿渣粉掺量的增大,水泥胶砂的各龄期抗折强度、3d抗压强度不断提高,7d、28d抗压强度在掺量为20%时达到最大值,之后有所降低。掺入超细矿渣粉后,能通过填充以及与水泥水化产物氢氧化钙发生反应,使水泥中氢氧化钙含量明显降低,水泥微观结构更加密实。     

矿物掺合料早期水化活性的测试和分析

本文采用环境扫描电子显微镜(ESEM)和热重-差热(TG-DTA)分析仪对磨细矿渣微粉、高钙粉煤灰、低钙粉煤灰的早期水化活性进行了系统测试和分析.理论和试验结果分析表明,掺合料取代水泥时,浆体早期抗压强度的提高取决于掺合料自身参与水化反应的速度和水化产物的数量.水化产物在掺合料颗粒表面沉积的速度和浆体中硅酸盐、铝酸盐水化产物的非蒸发水量随掺合料活性的提高而提高.掺合料活性按磨细矿渣微粉、高钙粉煤灰、低钙粉煤灰的顺序降低,将磨细矿渣微粉或高钙粉煤灰与低钙粉煤灰复合,可以克服低钙粉煤灰大掺量取代水泥时混凝土早期强度降低的缺陷,这是提高低钙粉煤灰在高强高性能混凝土中掺量的一个有效措施.     

The hydration properties of pastes containing municipal solid waste incinerator fly ash slag

This study investigated the hydration properties of Type I, Type III and Type V cements, mixed with municipal solid waste incinerator fly ash, to produce slag-blended cement pastes. The setting time of slag-blended cement pastes that contained 40% slag showed significantly retardation the setting time compared to those with a 10% or even a 20% slag replacement. The compressive strength of slag-blended cement paste samples containing 10 and 20% of slag, varied from 95 to 110% that developed by the plain cement pastes at later stages. An increased blend ratio, due to the filling of pores by C-S-H formed during pozzolanic reaction tended to become more pronounced with time. This resulting densification and enhanced later strength was caused by the shifting of the gel pores. It was found that the degree of hydration was slow in early stages, but it increased with increasing curing time. The results indicated that it is feasible to use MSWI fly ash slag to replace up to 20% of the material with three types of ordinary Portland cement.     

Fine limestone additions to regulate setting in high volume fly ash mixtures

High volume fly ash (HVFA) concrete mixtures are being considered more frequently due to their cost and sustainability advantages. While the long term performance of these HVFA concretes typically meets or exceeds that of conventional concretes, their early age performance is often characterized by excessive retardation of the hydration reactions, delayed setting times, and low strengths. Extending an HVFA mixture to a ternary blend that incorporates a fine limestone powder may provide a viable solution to these deficiencies, particularly the hydration retardation and setting issues. In this paper, a nano-limestone powder and two other limestone fillers of increasing median particle size (4.4 μm and 16.4 μm) are investigated for their propensity to accelerate early age reactions and reduce setting times in a Class C fly ash/cement blend. The fineness of the limestone has measurable effects on its efficacy in accelerating hydration and decreasing setting times. Companion specimens prepared with a fine silica powder suggest that the fine limestone may act favorably through both a physical and a chemical mechanism. Isothermal calorimetry and Vicat needle penetration measurements on pastes are accompanied by strength measurements on mortars, to verify that the limestone powder substitutions are not negatively impacting strength development. A linear relationship with a reasonable correlation is found to exist between 1 d and 7 d compressive strengths of mortars and their accompanying cumulative heat release values as determined using isothermal calorimetry.     

Rheological and hydration characterization of calcium sulfoaluminate cement pastes

Calcium sulfoaluminate (CSA) cements are currently receiving a lot of attention because their manufacture produces less CO₂ than ordinary Portland cement (OPC). However, it is essential to understand all parameters which may affect the hydration processes. This work deals with the study of the effect of several parameters, such as superplasticizer (SP), gypsum contents (10, 20 and 30 wt.%) and w/c ratio (0.4 and 0.5), on the properties of CSA pastes during early hydration. This characterization has been performed through rheological studies, Rietveld quantitative phase analysis of measured X-ray diffraction patterns, thermal analysis and mercury porosimetry for pastes, and by compressive strength measurements for mortars. The effect of the used SP on the rheological properties has been established. Its addition makes little difference to the amount of ettringite formed but strongly decreases the large pore fraction in the pastes. Furthermore, the SP role on compressive strength is variable, as it increases the values for mortars containing 30 wt.% gypsum but decreases the strengths for mortars containing 10 wt.% gypsum.     

The effect of temperature on the hydration of composite cements containing limestone powder and fly ash

The effect of the curing temperature (5, 20 and 40°C) on the degree of hydration, amount of bound water and calcium hydroxide, porosity and the development of mechanical properties was investigated on pastes and mortars prepared with fly ash (FA)?Climestone (L) Portland composite cements. Increasing the curing temperature for ordinary Portland cement (OPC) leads to a more inhomogeneous distribution of hydration products, resulting in an increased coarse porosity and therefore a lower compressive strength after 7?days and longer. In contrast, the FA containing mortars showed higher compressive strength with increasing curing temperature up to 90?days. The reaction of the FA is increased at 40°C and strongly retarded at 5°C. At 20 and 40°C, FA reduces the porosity at later ages. The replacement of 5% of the OPC or FA by L powder did not impair the strength at 5 and 20°C, but lowered strength slightly at 40°C for the FA blended cements. The porosity appears to be the dominating factor regarding the compressive strength, independent of whether part of the OPC is replaced by FA and L powder or not.     

矿物掺合料对地聚合物抗冻性能的影响

以碱激发偏高岭土制备地聚合物混凝土,分别研究了掺入15%的钢渣、矿渣或粉煤灰的地聚合物混凝土的力学抗压强度和抗冻性能,测试了地聚合物混凝土的真空饱水体积吸液率,运用XRD、SEM和DSC-TG等测试方法分析了矿物掺合料对地聚合物微观结构和水化产物的影响。结果表明:钢渣或矿渣能有效提高地聚合物混凝土的抗压强度,而粉煤灰的掺入使其强度稍有降低;地聚合物表观形貌中存在较多的孔洞和微裂缝导致其抗冻性能较差,掺入钢渣或者矿渣后地聚合物形成了新的产物C-S-H凝胶、C-A-S-H凝胶等并填充在结构中形成更加密实的板状结构,降低了地聚合物混凝土冻融破坏速率,五次冻融循环后地聚合物的相对强度均在90%以上,抗冻性能得到提高;粉煤灰降低了制备地聚合物混凝土的用水量且未水化的粉煤灰颗粒镶嵌在结构中增加了其密实性和抗冻性能,五次冻融循环后相对强度为86.9%,基准组的相对强度仅为79.7%。     

Investigation of the stability of hardened slag paste for the stabilization/solidification of wastes containing heavy metal ions

We have studied the effect of chromium ions and lead ions on the chemical stability of hardened slag paste with toxic wastes during the stabilization/solidification process. The influences of Cr and Pb ions on the hydration of slag were also investigated. Sodium silicate (Na(2)SiO(3)), 5 wt.% of slag, was used as an alkali activator for slag hydration. The physical stability of hardened paste containing partial replacement of slag with fly ash and gypsum was also examined.When gypsum was added to slag, the compressive strength of hardened slag paste developed, accompanying the activation of alumino-ferrite-tricalciumsulfate (Al(2)O(3)-Fe(2)O(3)-3CaSO(4), AFt) and alumino-ferrite-monocalciumsulfate (Al(2)O(3)-Fe(2)O(3)-CaSO(4), AFm) phase generation. Those phases caused densification of the microstructure. Concurrently, the leaching amount of heavy metal ions was decreased. When fly ash was added to slag, the compressive strength increased and the leaching amount decreased with both active formation of aluminate hydrates and ion substitution. Lead ions were mostly stabilized through physical encapsulation by the hardened slag paste's hydrate matrix. In the case of chromium ions, we observed that it was mainly solidified through the formation of a substitutional solid solution with aluminum atoms in the structure of aluminate hydrates.     

垃圾焚烧炉渣-粉煤灰复合水泥的性能研究

研究了垃圾焚烧炉渣及粉煤灰单掺和复掺时硬化水泥浆体的力学性能和水化机理,比较了两者的活性,探讨了两者作为辅助性胶凝材料利用的可行性.研究表明:掺有垃圾焚烧炉渣及粉煤友的复合水泥,其强度均有不同程度的下降,它们的掺入在一定程度上延缓了水泥的水化过程,且垃圾焚烧炉渣的水化反应活性稍高于粉煤灰;掺垃圾焚烧炉渣及粉煤灰的复合水泥中重金属离子浸出量小,在等掺20%的条件下,浸出量远低于国家标准,说明在一定的情况下,焚烧炉渣及粉煤灰作为辅助性胶凝材料使用是安全的.     

Synthesis of low-temperature calcium sulfoaluminate-belite cements from industrial wastes and their hydration: Comparative studies between lignite fly ash and bottom ash

The aim of this research was to study the production of calcium sulfoaluminate-belite (CŜAB) cement from industrial waste materials via hydrothermal-calcination process. Lignite fly ash and bottom ash were used as starting materials for comparison. Other waste materials viz., Al-rich sludge and flue gas desulfurization gypsum were also key players in raw mixes for the synthesis of CŜAB cement. For lignite fly ash as a starting material, mixed phases between ye'elimite and larnite were obtained, whereas for lignite bottom ash as starting material, only ye'elimite was obtained The hydration reaction was studied in terms of heat evolution, setting time, compressive strength and hydration product formation with various gypsum contents. The results showed a rapid formation of ettringite as a main hydration product mixed with calcium silicate hydrate, monosulfate and strätlingite phases as minority, with a fast final setting time of 24–26 min and high early compressive strength of 16.0 and 18.0 MPa in 1 day for CŜAB cements made of fly ash and bottom ash, respectively.     

固体废弃物对水泥基饰面砂浆性能的影响

采用正交分析法研究了矿粉、钢渣粉和脱硫石膏(FGD)等固体废弃物对饰面砂浆性能的影响。在满足JC/T1024-2007《墙体饰面砂浆》标准的要求下,固体废弃物可以取代50%以上的水泥,减少泛碱源。最佳正交配比为矿粉、钢渣粉和脱硫石膏分别取代水泥用量的40%、10%和8%,制备出的饰面砂浆的抗折抗压强度、拉伸粘接强度、吸水量及抗泛碱性均较好。