水泥净浆结粒水筛检测方法研究

由水筛法得到启示，提出了一套水泥净浆结粒的检测方法。通过研究水泥称量、水化温度、水泥细度、水灰比、石膏掺量和水化时间对结粒量的影响，探讨了该检测方法的可行性，并计算了结粒量的标准偏差。结果表明：该净浆结粒检测方法可靠性高，检测结果具有很好的稳定性和重现性；同时对于不同条件下的变化，能够充分反映水泥净浆结粒的变化规律，是研究净浆结粒的有效方法。     

不同黏土对掺减水剂水泥净浆流动度影响

目的 研究4种不同黏土对掺聚羧酸减水剂及萘系减水剂水泥净浆流动度的影响规律并从黏土的吸附性能角度探究其影响机理.方法 采用水泥净浆流动度试验方法比较了4种黏土对掺聚羧酸减水剂水泥净浆流动度的影响,通过TOC总有机碳测试仪测定了4种黏土对聚羧酸减水剂的吸附量.结果 4种黏土对水泥净浆流动度的影响差异较大,其中钙基蒙脱土和钠基蒙脱土的掺量为2％时,掺聚羧酸减水剂水泥净浆已基本没有流动度,掺萘系减水剂的水泥净浆流动度也有所下降,但降幅稍小,而伊利土和高岭土对掺减水剂水泥净浆流动度无明显负面影响;钙基蒙脱土和钠基蒙脱土对聚羧酸减水剂的吸附量较大,伊利土、高岭土对聚羧酸减水剂的吸附能力和水泥相当.结论蒙脱土对掺聚羧酸减水剂水泥净浆流动度负面影响极为严重,而伊利土和高岭土对掺减水剂水泥净浆基本没有负面影响.     

石膏掺量对高贝利特-硫铝酸盐水泥性能的影响

利用循环流化床(CFBC)固硫灰代替部分铝矾土、石膏等原料制备高贝利特-硫铝酸盐水泥,并采用XRD、SEM等方法研究了石膏掺量对该水泥凝结时间、抗压强度、水化产物和微观结构的影响。结果表明,利用固硫灰等原料制备的水泥熟料的矿物组成主要有C2S、C4A3S、铁相等;掺入石膏会缩短水泥的凝结时间,最佳石膏掺量为9%;水泥3d、28d净浆强度可以达到39.00MPa和82.59MPa;掺入适量石膏能促进C4A3S和C2S水化,掺量不足会使AFt向AFm转化,掺量过大反而会阻碍C4A3S的水化,进而影响水泥强度;不同石膏掺量下的水泥水化产物主要为AFt、AFm、C-S-H凝胶和铝胶等。     

石膏的形态对C2S浆体强度的影响

研究了二水石膏、600℃、800℃、1000℃煅烧石膏对C2S浆体强度的影响，结果表明：石膏的掺入，能提高C2S浆体的强度；煅烧石膏比二水石膏更能提高C2S浆体的强度。证明了石膏不仅对硅酸盐水泥中C3A的水化产生影响，同时亦对硅酸盐矿物的水化有促进作用。     

氧化石墨烯分散液对水泥净浆水化和力学性能 影响机理分析

为研究氧化石墨烯(GO)掺量对水泥净浆水化和力学性能的影响,采用改进Hummers法和超声波分散法制备GO片层分散液,利用傅里叶红外光谱(FTIR)和X-射线衍射(XRD)表征GO;研究了GO掺量对水泥净浆抗压、抗折强度的影响规律,并从微观角度揭示了GO分散液对水泥净浆的调控机理。结果表明:与普通水泥净浆相比,掺入适量的GO能够促进水泥水化进程,提高水泥净浆中的化学水结合量,水化晶体互相缠绕、交织形成规整有序的多面体状微结构,使水泥净浆的早期力学性能显著提高,最佳GO掺量为水泥质量的0.03%。适量的GO能够提高水泥净浆的抗压和抗折强度,促进水泥净浆水化晶体的生长,改变晶体的尺寸和形状,实现对水泥净浆微结构的调控。     

混合材对高C3S含量水泥水化性能的影响

通过测定不同龄期和掺量的煤矸石-水泥、超细粉煤灰-水泥复合体系力学性能、结合水量及混合材反应程度，并结合XRD研究了低水胶比下超细粉煤灰、活化煤矸石对高C3S含量水泥水化性能的影响。试验结果表明，粉煤灰的化学效应对高C3S含量水泥早期水化的影响与煤矸石相差不大，但是其物理特性对高C3S含量水泥早期强度的影响要高于煤矸石；而活化后的煤矸石对高C3S水泥后期水化的影响优于超细粉煤灰，其抗压强度、结合水量和混合材反应程度均高于粉煤灰-水泥复合体系；活化煤矸石单独与高C3S水泥复合使用时，其掺量可比Ⅱ级粉煤灰提高20％。     

搅拌时间对粉煤灰水泥净浆流动性及早期抗压强度的影响

影响粉煤灰水泥净浆的流动性与早期抗压强度等问题一个重要原因就是拌合是否充分,搅拌时间是否合适。现有的相关规范中对于拌合时间的规定大都针对普通混凝土,随着高性能混凝土的发展,尤其是粉煤灰混凝土近几年来的广泛使用,导致现有的拌合时间规定无法满足粉煤灰混凝土均匀性的控制要求。为此,通过初步研究不同拌合时间对不同掺量的粉煤灰水泥净浆流动性及早期抗压强度的影响,最终确定合理的粉煤灰水泥净浆拌合时间,供进一步研究与工程应用参考。     

木素磺酸钙对水泥净浆的缓凝机理研究

研究了掺加木素磺酸钙(简称木钙)后水泥净浆液相中钙离子、硫酸根离子和氢氧根离子浓度随水化时间的变化,以及除糖后木素磺酸钙对水泥净浆凝结时间的影响．结果表明,掺加木钙后在水化初期水泥净浆中S042-浓度大幅度上升,OH-浓度变化不大．木钙掺量越大,水泥净浆中游离Ca2 浓度的峰值出现越迟,浆体的初凝时间越长．进一步研究发现木钙的掺加能促进熟料矿物的水解,当木钙掺量为0．5％(质量分数)时,水泥净浆中的总Ca2 浓度峰值比未掺加木钙时增加48％,被络合的Ca2 量峰值较水化开始时增加2倍．在水泥净浆强碱性溶液中木钙的络合能力增强导致Ca(OH)2不能达到过饱和,是造成水泥净浆缓凝的重要原因,木钙对水泥净浆的缓凝机理为“吸附-络合”机理．     

矿粉对水泥和混凝土性能的影响

为了探寻矿粉细度及掺入量对水泥和混凝土性能的影响,通过试验测试方法,分析了矿粉和水泥的基本性质,研究了超细矿粉和普通矿粉的掺量对水泥基材料标准稠度、凝结时间、流动度和力学性能的影响.结果表明：普通矿粉使水泥净浆标准稠度需水量下降,而超细矿粉则增加标准稠度需水量,两种矿粉都使水泥净浆凝结时间略微延长.普通矿粉可以改善水泥净浆的流动度,超细矿粉的加入则降低了水泥净浆的流动度.普通矿粉和超细矿粉降低水泥净浆早期（7 d）抗压强度,提高后期（28 d）抗压强度,掺10％～50％的普通矿粉的水泥净浆28 d抗压强度提高2.9％～9.7％,掺入超细矿粉28 d抗压强度提高3.9％～20.1％,普通矿粉和超细矿粉的最佳掺量为10％～30％;两种矿粉替代10％～50％水泥所配制的混凝土的强度得到了明显的提高.     

硅灰对水泥净浆抗硫酸盐侵蚀性能的改善作用

将水泥净浆试件在5%Na2SO4溶液中长期浸泡,用试件强度随浸泡时间的变化和试件中物相的XRD分析,研究了硅灰对水泥净浆抗硫酸盐侵蚀性能的影响.在Na2SO4溶液侵蚀下,普通硅酸盐水泥净浆试件强度随浸泡时间先增长,然后急剧降低;外观和XRD相分析表明,其原因是由于形成了膨胀性钙矾石,造成试件开裂破坏;加入硅灰的水泥净浆试件强度损失明显减小,尤其是抗折强度没有降低,其抵抗强度下降系数还略有增加;原因是由于硅灰的稀释作用和火山灰效应减少了水泥净浆中Ca(OH)2的量,从而降低了水泥净浆试件在硫酸盐溶液侵蚀下形成的膨胀性钙矾石的量.因而,硅灰对水泥混凝土抗硫酸盐侵蚀性能有改善作用.     

Influence of New Compound Admixture on Shotcrete Performance

To analyze the influence of new compound admixture on shotcrete performance, the ordinary Portland cement pr425 was used as matrix components. The optimum proportion of admixture was obtained by analyzing the influence of content on cement setting time and compressive strength. The microstructure of cement test block and the mechanism of reducing dust of composite macromolecule admixture were analyzed by scanning electron microscopy and infrared spectroscopy. It was shown that the ratio of polyacrylic acid was 0.02%. The ratio of J85 accelerator was 5%. The ratio of bentonite was 4.5% in composite admixture. The most optimal content of admixture in the slurry was 7%. The compound coagulant formed by additive together with C_3 A, C_4 AF which provided nucleation for hydration and crystallization of C_3S and C_3S, and played an active role to promote the activity of the mineral admixture in cement, and increased the elastic modulus of C-S-H gel and accelerated the hydration process of portland cement. Bentonite and polyacrylic acid promote the wettability, cohesiveness and workability of cement paste in the process of hydration. The formation of cement test block gel was even. The interface between the matrix phase and the aggregate phase was not obvious which ensured the matching between the matrix and the aggregate phase. The addition of bentonite formed hydrogen bonds in cement paste and improved the cohesiveness of the system. The J-85 accelerator promoted the combination of aluminate and gypsum which hindered the formation of calcium carbide around the cement particles which made cement rapid condensation. Polyacrylic acid mainly changed the strength of hydroxyl absorption peak in cement paste to improve the initial strength of cement test block. The addition of new admixtures promoted the process of cement hydration to be more thorough and affected the later strength development of concrete by affecting the formation of calcium carbonate stone.     

偏高岭土对水泥净浆火山灰效应强度贡献率的影响

根据蒲心诚教授提出的偏高岭土火山灰效应定量分析方法,进行了偏高岭土对水泥净浆(以下简称净浆)火山灰效应强度贡献率(以下简称强度贡献率)的影响研究.结果表明:随着偏高岭土掺量的增加,其净浆强度贡献率增加;随着养护龄期的增加,其净浆强度贡献率呈现先减少后增加的趋势,且7,d时出现最低值;3、28,d时小粒径偏高岭土(2.5和3.75,μm)的净浆强度贡献率明显高于7,d时的值,这说明偏高岭土火山灰效应主要是发生在早期(3,d)和后期(28,d);而大粒径偏高岭土和补充激发剂则有利于提高其中期(7,d)净浆强度.     

基于水膜厚度假设分析磨细高炉矿渣对水泥浆性能影响

为探索磨细高炉矿渣对水泥浆性能及其水膜厚度的影响,研究测量了30组不同水胶比、不同磨细高炉矿渣掺量的水泥–;矿渣复合浆体的流动性能、黏聚性和抗压强度.为探索浆体的流变性能控制机理,进一步测量了5组不同磨细高炉矿渣掺量水泥–;矿渣复合浆体的填充密度,并基于填充密度测量结果计算出各浆体试样配比的水膜厚度,探索水膜厚度对水泥–;矿渣复合浆体流变性能的影响.实验结果表明,适量磨细高炉矿渣的掺入能提高浆体的流动性能和抗压强度,黏聚性些许减弱,最优配比磨细高炉矿渣掺量为5%,此时水泥–;矿渣复合浆体综合性能最好.磨细高炉矿渣掺入能提高胶凝材料的填充密度,水膜厚度为流动性主要控制因素,水泥浆的流动性能随水膜厚度增大而增大.     

功能调整材料对水泥浆体流动性影响

使用自行研制的H管分别研究了不同功能调整材料对水泥浆体流动性的影响,得到不同种类矿物掺合料和增稠剂对水泥浆体流动性改性规律:粉煤灰掺量的增加引起浆体流动性先增加后减小;矿粉掺量越大,浆体流动性越大;硅灰和增稠剂掺量越大,浆体流动性越差。H管对水泥浆体流动性变化十分敏感,可以准确快速评价不同功能调整材料对水泥浆体流动性影响。     

Preparation and Mechanism Research of Hydrationheat-inhibiting Materials with Microcapsule Sustained-releasing Technology

Hydration-heat-inhibiting materials(HIM) with polysaccharide as core material was prepared using microcapsule sustained-releasing technology,through a centrifugal spray granulation process after melting together.The preparation process parameters of HIM were selected by the semi-adiabatic temperature rise test of cement paste.TAM air microcalorimeter was used to investigate the regulation performance of HIM on the hydration of cement.The influence of HIM on the microstructure of cement was investigated by XRD,SEM,and TG-DSC.The results showed that the most suitable wall material for HIM was polyethylene wax,the optimum polyethylene wax/polysaccharide mass ratio was 1,and the most effective particle size was 0.16-0.30 mm.Polysaccharide coated by polyethylene wax released slowly,and the peak heat release rate of cement could be reduced by 55.2% after continuous regulaion.The regulation period continued to 120 h.HIM mainly decreased the C_3S reaction rate,which resulted in a 39.2% peak value reduction of hydration heat release rate.However,HIM had little regulation on C_3A.The hydration heat release process of cement-based materials can be designed by adjusting the dosage of HIM.     

Dynamic elastic modulus of cement paste at early age based on nondestructive test and multiscale prediction model

This paper introduced a nondestructive testing method to evaluate the dynamic elastic modulus of cement paste. Moreover, the effect of water-cement ratio and conventional admixtures on the dynamic elastic modulus of cement paste was investigated, in which three kinds of admixtures were taken into account including viscosity modifying admixture （VMA）, silica.fume （SF）, and shrinkage-reducing admixture （SRA）. The experimental results indicate that the dynamic elastic modulus of cement paste increases with decreasing water-cement ratio. The addition of SF increases the dynamic elastic modulus, however, the overdosage of VMA causes its reduction. SRA reduces the dynamic elastic modulus at early age without affecting it in later period. Finally, a multiscale micromechanics approach coupled with a hydration model CEMHYD3D and percolation theory is utilized to predict the elastic modulus of cement paste, and the predictive results by the model are in accordance with the experimental data.     

Mechanism of Thaumasite Formation in Concrete

Significant efforts have been made in revealing the mechanism of thaumasite formation in concrete, which continues to be fraught with ambiguities and dissension. Chemical method was employed to synthesize pure C_3S, C_2S, C_3A, ettringite, and thaumasite, and X-ray diffraction(XRD), Raman spectroscopy and infrared spectroscopy(IR) were used to identify thaumasite from other hydrates. To investigate the direct route of thaumasite formation, C_3S, C_2S, gypsum, and calcium carbonate were used to prepare a cement paste so that the interference of ettringite formation can be avoided. The indirect route of thaumasite formation was also studied by considering the effect of C_3A or ettringite content on thaumasite formation. Results show that thaumasite can be definitely generated in the absence of aluminium-bearing minerals or ettringite under appropriate conditions, while the ettringite presence promotes the thaumasite formation. No evidences support the heterogeneous nucleation route in this work. It is concluded that the method mentioned in this work can surely be used to investigate the mechanism of thaumasite formation, and thaumasite can form by both direct and woodfordite routes.     

UNIFORMITY ASSESSMENT OF CARBON FIBRES DISPERSION IN CEMENT PASTE BY IMPEDANCE MEASUREMENTS

An alternating current was applied to measure the impedance of a hardened cement paste with various contents of carbon fibres. When the free water content in the hardened cement paste is 90%-98%, and the measuring frequency 500Hz, an approximate linear relationship was found between fibre content and impedance of the composite. Based on this relationship , a new attempt was made to evaluate the dispersion uniformity of carbon fibres in cement paste by impedance measurement. The standard deviation S and the coefficient of vriation S/Xi     

磺化淀粉-聚羧酸复合减水剂的制备与表征

由于保护环境的原因,以天然高分子为原料来合成高效减水剂已经成为混凝土外加剂研究领域的新热点.本文研究了采用磺化糊精取代部分功能大单体来合成复合聚羧酸减水剂的方法.结果显示:当磺化糊精取代功能单体40%、复合聚羧酸减水剂掺量为0.5%时,水泥净浆的初始流动度达255,mm,1,h 后其流动度仍为250,mm.淀粉酸解后,增加亲水的羟基基团导致初期水化缓慢,而增加 Zeta 电位使水泥颗粒更易于分散.在复合减水剂中,长链 Starch 与短链的聚羧酸减水剂主链将被吸附于水泥颗粒表面上,交替发生静电与空间位阻作用,起到了增加减水率和降低缓凝的效果.