共查询到20条相似文献,搜索用时 78 毫秒
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以垃圾焚烧(MSWI)飞灰为主要原料,在实验室成功烧制了硫铝酸钙(CSA)水泥熟料,继而着重研究了不同种类和不同掺量的石膏对CSA水泥的抗压强度、水化性能、标准稠度用水量和凝结时间的影响;研究了细度对CSA水泥性能的影响。结果表明:无水石膏和二水石膏均促进C4A3S^-水化,提高CSA水泥的早期强度;无水石膏的最佳掺量是5%,二水石膏可根据实际情况进行调整;掺加无水石膏的CSA水泥其标准稠度用水量较对照水泥C—II低,比对照水泥C—I有所增加;掺加5%无水石膏后水泥的凝结时间与对照水泥C-II接近,当掺量增至10%后出现急凝。本试验中,CSA水泥比表面积在288—580m^2/kg范围时均表现出良好的力学性能。 相似文献
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通用水泥实施ISO标准后的效果和需解决的问题 总被引:2,自引:0,他引:2
我国通用水泥实施GB/T17671-1999〈水泥胶砂强度检验方法(ISO法)〉已经1年多了。作为起草单位,我们和水泥界的同行们一样,非常关心它的实施效果和存在的问题。2002年6月份,我们协助中国建材协会对通用水泥标准实施情况进行了一次问卷调查,调查对象包括各省行业管理办公室和协会、省水泥质检站、施工单位以及水泥企业等4个方面。通过这项工作,使我们对ISO强度检验方法的实施效果有了了解,现就此做一总结归纳,并提出需进一步研究和解决的问题。1对我国通用水泥基本性能的影响1.1抗压强度和产品标号(等级… 相似文献
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试验选用三乙醇胺、二乙烯三胺,三异丙醇胺,氨基乙基乙醇胺,聚乙烯醇磷酸铵作为早强剂,研究其在微小掺量下对硅酸盐水泥标准稠度用水量、凝结时间、与外加剂的适应性、胶砂强度等方面的影响。试验结果表明,醇胺类化合物的掺加对水泥标准稠度用水量产生了增大的趋势;三乙醇胺与N-(2-羟乙基)乙二胺明显的缩短了水泥的初凝时间与终凝时间,三异丙醇胺、二乙烯三胺延长了水泥的初凝时间,缩短了水泥的终凝时间;三异丙醇胺与N-(2-羟乙基)乙二胺在0.2‰掺量时对水泥的流动度无影响,N-(2-羟乙基)乙二胺在0.1‰掺量时,使水泥的流动度得到增加,其它组均对水泥与外加剂的适应性造成不良影响;除了三异丙醇胺在掺量为0.20‰与0.50‰时的早期强度低于空白水泥之外,其他各组都有不同程度的增加,后期强度,三异丙醇胺在任何掺量下,明显强于三乙醇胺。 相似文献
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通过对多家同品种水泥的净浆试验比对,对现行国家标准GB/T1346—2001中关于代用法测定水泥标准稠度用水量的部分条款存有歧意。试验研究表明,当试锥下沉深度在26口2mm范围内,不同拌和水量下的凝结时间极差较小,超出此范围会有显著增大。 相似文献
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试杆法比试锥法对水泥标准稠度用水量的反映更为敏感,在检验工作中应尽量采用试杆法测定水泥的标准稠度用水量。用试锥法测定的具有标准稠度的水泥净浆,用来测定水泥凝结时间时,普遍比用试杆法的测定结果略短一些。在实际工作中,如果采用试锥法测定水泥的标准稠度用水量时,应选用试锥下沉深度在(29±1)mm的范围,具有这样标准稠度的水泥净浆用来测定水泥的凝结时间,才能够使其和用试杆法检测所得的水泥标准稠度用水量相对接近,才更加合理,减少实验误差,从而保征水泥凝结时间检验结果的准确性。 相似文献
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制备MgO质量分数分别为6%、9%、12%和15%的高镁水泥,通过扫描电镜(SEM)、扫描电镜/能谱联合仪(SEM/EDS)、X射线衍射(XRD)等检测方法和膨胀性试验分析MgO质量分数对熟料煅烧和净浆膨胀性能的影响.结果表明:随着MgO质量分数增加,熟料煅烧时液相量增加,熟料密实度提高.当熟料中MgO质量分数为12%时,养护温度由20℃增加到38℃,试件90d龄期膨胀率由0.120%增加到0.244%;38℃养护时,掺入35%粉煤灰的试件90d龄期膨胀率由0.244%降至0.070%.当MgO质量分数高于12%时,尽管存在粉煤灰的抑制作用,但高镁水泥依然能产生一定膨胀,可以有效地补偿混凝土的温降收缩. 相似文献
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A setting time parameter has been determined from the heat evolution versus time curve measured by means of a thermocouple embedded in the cement paste as well as by the Gillmore needle. The setting time increases with increasing temperature, until it reaches a maximum between 26 and 30°C, for four out of the five refractory calcium aluminate cements studied. This anomalous retardation is not, therefore, restricted to ciment fondu, as reported elsewhere. The rate of consumption of CA during the first 24 hours of hydration as determined by X-ray diffraction also indicated a retardation at 30°C compared with 20°C for Secar 51 and Secar 71. The cause of the anomaly cannot be the presence of C2S, which is virtually absent in most of the cements studied. An alternative explanation must be found, which should also explain why Secar 80 behaves differently from the other cements investigated. 相似文献
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This work reports a kinetic study of the formation of magnesium-potassium phosphate cements accomplished using in-situ synchrotron powder diffraction. The reaction: MgO + KH2PO4 + 5H2O → MgKPO4 · 6H2O was followed in situ in the attempt of contributing to explain the overall mechanism and assess the influence of periclase (MgO) grain size and calcination temperature (1400-1600 °C) on the reaction kinetics. Numerical kinetic parameters for the setting reaction have been provided for the first time. The best fit to the kinetic data was obtained using a weighted nonlinear model fitting method with two kinetic equations, representing two consecutive, partially overlapping processes. MgO decomposition could be described by a first order (F1) model followed by a Jander diffusion (D3) controlled model. Crystallization of the product of reaction was modelled using an Avrami model (An) followed by a first order (F1) chemical reaction. A reaction mechanism accounting for such results has been proposed. 相似文献
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Bond strength and chemical interaction of self-adhesive resin cements according to the dentin region
The aim of the study is to evaluate the effectiveness and level of chemical interaction of self-adhesive resin cements (SRCs) according to the dentin region. One hundred eight sound human third molars and three SRCs were selected: Bifix SE (Voco), Maxcem Elite (Kerr), and RelyX U200 (3M ESPE). Ninety human molars were used for the bond strength test and 18 teeth for the X-ray diffraction (XRD) characterization. A flat surface of superficial, deep, or axial dentin was exposed. For bond strength evaluation, 90 indirect composite resin restorations (10 mm in diameter, 2.0 mm-thick) were built and cemented with one of the SRCs according to the manufacturer's instructions. The restored teeth were then cut into sticks with cross-sectional areas of 0.8 mm2 and tested in tensile at a speed of 0.5 mm/min (n=10). The results of bond strength were statistically analyzed by two-way ANOVA and Tukey's test (α=0.05). The fractured specimens were classified under SEM. The remaining teeth were further sectioned in order to build dentin fragments with 2.0 mm2 of area and 0.2 mm in thickness for XRD analysis. In general, significantly higher bond strength was found when bonding to axial and deep dentin compared to superficial dentin. Comparing the bonding effectiveness of the SRCs, taking into account the mean bond strength obtained in the 3 dentin regions, the study found no significant difference (p>0.05). Although RelyX U200 showed similar bond strength irrespective of the dentin region (p>0.05), the bonding results of the other 2 SRCs varied significantly (p<0.05). There was a higher incidence of cohesive failure in the SRCs for all groups. The XRD analysis detected different perceptual reductions of hydroxyapatite crystallinity for all SRCs, indicating a particular chemical interaction in each experimental condition. Thus, it can be concluded that the bond strength and chemical interaction of the SRCs can vary significantly according to the dentin region. 相似文献
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维生素E脂质体的制备与性能研究 总被引:5,自引:0,他引:5
采用薄膜蒸发-高压均质法制备维生素E(VE)脂质体,研究了VE脂质体配方中不同成分的比例及水合介质对脂质体包封率的影响。结果表明,VE脂质体载药量越大,包封率越低。胆固醇含量在体系中要适当。最佳的水合介质是磷酸盐缓冲液。采用薄膜蒸发结合高压均质处理法制备的VE脂质体粒径达到120nm,而且比较稳定。 相似文献