Anti-Crack Performance of Low-Heat Portland Cement Concrete

The properties of low-heat Portland cement concrete（LHC） were studied in detail. The experimental results show that the LHC concrete has characteristics of a higher physical mechanical behavior, deformation and durability. Compared with moderate-heat Portland cement（MHC）, the average hydration heat of LHC concrete is reduced by about 17.5%. Under same mixing proportion, the adiabatic temperature rise of LHC concrete was reduced by 2 ℃-3 ℃,and the limits tension of LHC concrete was increased by 10× 10^-6-15×10^-6 than that of MHC. Moreover, it is indicated that LHC concrete has a better anti-crack behavior than MHC concrete.

Effect of Hydrated Calcium Aluminate Cement on the Chloride Immobilization of Portland Cement Paste

To improve the efficiency and stability of chloride immobilization of portland cement paste,hydrated calcium aluminate cement(HCAC)prepared by wet grinding of CAC was added into portland cement paste as an additive.The immobilized chloride ratio(ICR)was evaluated,and the mechanism of chloride immobilization was researched by XRD,DTG,NMR,and MIP tests.The analysis results demonstrated that HCAC could improve the chloride immobilization capacity of portland cement paste.The mechanism was attributed to the following aspects:chemical binding capacity was enhanced via producing more Kuzel’s salt;physical adsorption capacity was reduced by decreasing the C-S-H gel;migration resistance was enhanced through refining the pore structure.

Research Progress of Eco-Friendly Portland Cement Porous Concrete:A Review

With the great impetus of energy conservation and emission reduction policies in various countries,the proposal of concepts such as“Sponge City”and“Eco-City”,and the emphasis on restoration and governance of ecological environment day by day,portland cement porous concrete(PCPC),as a novel building material,has attracted more and more attention from scientific researchers and engineers.PCPC possesses the peculiar pore structure,which owns numerous functions like river embankment protection,vegetation greening as well as air-cleaning,and has been of wide application in different engineering fields.This paper reviews the salient properties of PCPC,detailedly expounds the research progress of domestic and foreign literature about this subject in the past ten years(2010–2020),conducts the statistical analysis of the distribution rule of its major properties around the world,combines with the engineering application to summarize the excellent properties of PCPC,and makes a forecast of future research direction.

Portland Cement用于根尖屏障材料的封闭性研究

目的通过离体实验观察波特兰水门汀(Portland Cement,PC)作为根尖屏障的封闭性,并将其与无机三氧化物聚合物(mineral trioxide aggregate,MTA)、玻璃离子水门汀(glass ionomer cement,GIC)、银汞合金(amalgam,Am)作比较。方法选取单根前磨牙64颗,行根管预备并制备根尖开放模型。完全随机分组法将实验用离体牙分为A、B、C、D 4个实验组,根尖部分别充以PC、MTA、GIC、Am,每组15个样本,阴性对照组及阳性对照组每组各2个样本。使用4%牛血清白蛋白作为观测指标连续观测60 d,用考马斯亮蓝染色技术对蛋白渗出做定量测定。结果 A组与B组蛋白渗出量无明显统计学差异,A组与C、D组蛋白渗出量比较有统计学差异(P<0.05),B组与C、D组蛋白渗出量比较有统计学差异(P<0.05)。随着时间的延长,A组蛋白渗出量的增加无统计学意义。结论 PC的根尖封闭性与MTA相当,且明显优于GIC、Am。

Portland cement修复磨牙髓室底穿孔的实验研究

目的评估波特兰水门汀(Portland cement,PC)直接修复磨牙髓室底穿孔的效果,并与无机三氧化聚合物(mineral trioxide aggregate,MTA)作比较。方法选取人新鲜拔除的恒磨牙53颗,按随机数字表法分为PC、MTA2个实验组(n=24)和1个对照组(n=5)。实验组在髓室底中央制备直径2 mm的穿孔模型,分别用PC和MTA修复穿孔。对照组只开髓不制备穿孔模型。利用体视显微镜观察修复后样本的根分叉形态。扫描电子显微镜(SEM)观察材料和牙体组织的结合界面,并测量结合界面间隙宽度。采用葡萄糖定量法分析模型检测微渗漏值。结果体视显微镜下两实验组对根分叉外形修复均达到了良好效果。SEM观察显示PC和MTA与牙体组织之间均可见不连续的微间隙存在,PC与牙体组织间隙宽度为(7.363±2.159)μm,MTA与牙体组织间隙宽度为(8.693±3.551)μm,两者无明显差异(P>0.05)。在观察期内,虽然PC组的微渗漏值小于MTA组,但无统计学差异(P>0.05)。结论 PC与MTA修复髓室底穿孔的封闭效果相当,且PC价格低廉,不易使牙体变色,可以考虑作为MTA替代材料进一步研究。

加显影剂的Portland cement作为根充材料的封闭性研究

目的通过染料渗透+透明标本法评价白色波特兰水门汀(white Portland cement,WPC)、WPC+氧化铋(Bi2O3,BO)、WPC+氧化锆(ZrO2,ZO)、无机三氧化聚合物(mineral trioxide aggregate,MTA)和灰色波特兰水门汀(gray Portland cement,GPC)作为根管充填材料的封闭性能。方法选取单根离体前磨牙104颗,制作根尖倒充填模型,按随机数字表法将离体牙分成5个实验组(WPC、WPC+BO、WPC+ZO、MTA、GPC组,n=20)和2个对照组(阴性对照组、阳性对照组,n=2)。染料渗透法检测根尖微渗漏情况,体视显微镜下测量染料自根尖渗入冠方的长度。结果阳性对照组染料渗入整个根管,阴性对照组无染料渗入,WPC、WPC+BO、WPC+ZO、MTA 4组仅有微量染料渗入,且4组染料渗入深度两两比较差异无统计学意义(P>0.05),GPC组有较多的染料渗入,渗入深度与前4组比较差异有统计学意义(P<0.01)。结论WPC、WPC+BO、WPC+ZO与MTA封闭性相当,且它们的封闭性明显优于GPC;ZO和BO可考虑作为显影剂加入WPC中。

Properties of high calcium fly ash geopolymer pastes with Portland cement as an additive

The effect of Portland cement （OPC） addition on the properties of high calcium fly ash geopolymer pastes was investigated in the paper. OPC partially replaced fly ash （FA） at the dosages of 0, 5%, 10%, and 15% by mass of binder. Sodium silicate （Na2SiO3） and sodium hydroxide （NaOH） solutions were used as the liquid portion in the mixture： NaOH 10 mol/L, Na2SiO3/NaOH with a mass ratio of 2.0, and alkaline liquid/binder （L/B） with a mass ratio of 0.6. The curing at 60℃ for 24 h was used to accelerate the geopolymerization. The setting time of all fresh pastes, porosity, and compressive strength of the pastes at the stages of 1, 7, 28, and 90 d were tested. The elastic modulus and strain capacity of the pastes at the stage of 7 d were determined. It is revealed that the use of OPC as an additive to replace part of FA results-in the decreases in the setting time, porosity, and strain capacity of the paste specimens, while the compressive strength and elastic modulus seem to increase.

Effect of Fine Steel Slag Powder on the Early Hydration Process of Portland Cement

Hydration heat evolution, non-evaporative water, setting time and SEM tests were peorormed to investigate the effect of fine steel slag powder on the hydration process of Portland cement and its mechanism. The results show that the effect of fine steel slag powder on the hydration process of Portland cement is closely related to its chemical composition, mineral phases, fineness, etc. Fine steel slag powder retards the hydration of portland cement at early age. The major reason for this phenomenon is the relative high content of MgO , MnO2, P2O5 in steel slag, and MgO solid solved in C3 S contained in steel slag.

Effects of fibers on expansive shotcrete mixtures consisting of calcium sulfoaluminate cement,ordinary Portland cement,and calcium sulfate

The mining industry often uses shotcrete for ground stabilization. However, cracking within shotcrete is commonly observed, which delays production schedules and increases maintenance costs. A possible crack reduction method is using expansive shotcrete mixture consisting of calcium sulfoaluminate cement(CSA), ordinary Portland cement(OPC), and calcium sulfate(CS) to reduce shrinkage. Furthermore, fibers can be added to the mixture to restrain expansion and impede cracking. The objective of this paper is to study the effects of nylon fiber, glass fiber, and steel fiber on an expansive shotcrete mixture that can better resist cracking. In this study, parameters such as density, water absorption, volume of permeable voids, unconfined compressive strength(UCS), splitting tensile strength(STS), and volume change of fiber-added expansive mixtures were determined at different time periods(i.e. the strengths on the 28 th day, and the volume changes on the 1 st, 7 th, 14 th, 21 st, and 28 th days). The results show that addition of fibers can improve mixture durability, in the form of decreased water absorption and reduced permeable pore space content. Moreover, the expansion of the CSA-OPC-CS mixture was restrained up to50% by glass fiber, up to 43% by nylon fiber, and up to 28% by steel fiber. The results show that the STS was improved by 57% with glass fiber addition, 43% with steel fiber addition, and 38% with nylon fiber addition. The UCS was also increased by 31% after steel fiber addition, 26% after nylon fiber addition, and16% after glass fiber addition. These results suggest that fiber additions to the expansive shotcrete mixtures can improve durability and strengths while controlling expansion.

The Durability of Alkali-Activated Materials in Comparison with Ordinary Portland Cements and Concretes:A Review

China is the largest producer and user of ordinary Portland cement(OPC),and the rapid growth of infrastructure development demands more sustainable building materials for concrete structures.Alkali-activated materials(AAMs)are a new type of energy-saving and environmentally friendly building material with a wide range of potential applications.This paper compares the durability of AAMs and 0 PC-based materials un der sulfate attack,acid corrosion,carb on ation,and chloride penetratio n.Different AAMs have shown distinct durability properties due to different compositions being formed when different raw materials are used.According to the calcium(Ca)concentration of the raw materials,this paper interprets the deterioration mechanisms of three categories of AAMs:calcium-free,low-calcium,and calcium-rich.Conflicts found in the most recent research are highlighted,as they raise concerns regarding the consistenee and long-term properties of AAMs.Nevertheless,AAMs show better durability performances than OPC-based materials in general.

Serviceability and Reinforcement of Low Content Whisker in Portland Cement

In order to explore the serviceability and reinforcement of CaCO3 whisker in portland cement matrix, the durability of CaCO3 whisker and effect of low whisker content（0%-4.0%） on the working performance and mechanical properties of portland cement were investigated. The experimental results show that CaCO3 whiskers have a good stability and serviceability in cement, and should not significantly alter the rheological properties of the cement paste. The flexural and compressive strength of portland cement reinforced by CaCO3 whiskers was increased by 33.3% and 12.83%, respectively.

Morphology Difference between the Alkali Activated Cement and Portland Cement Paste on Multi-scale

The features of alkali activated slag（AAS） and portland cement （PC） were observed on multi-scale,the crack and fracture sections were observed with naked eyes,and SEM and AFM were used to study the structure morphology differences between PC and AAS on micrometer to nano meter scale.The experimental results indicated that the AAS paste had soil like fracture texture and it was composed of mainly C-S-H gel but lacks of crystals,and it had a very strong tendency to shrink and crack.AAS paste is much denser and more homogeneous than PC,and on the nano scale C-S-H nano particle in the AAS paste is much smaller and packs much denser than PC paste.

Effect of Calcium Aluminate Cement Variety on the Hydration of Portland Cement in Blended System

Two kinds of CACs with different monocalcium aluminate（CA） contents were used in the PC/CAC（PAC） mixtures. Effects of CA and CACs on the properties of PAC were analyzed by setting times and the compressive strength tests, and also by means of calorimetry, XRD, DTA-TG and ESEM. The experimental results show that the compressive strength of the PAC mortars decreases with increasing content of CAC while it declines sharply with a higher content of CA in CAC. Compared with neat PC paste, the content of calcium hydroxide in hydrates of PAC paste decreases significantly, and the hydration time of PC is prominently prolonged. Additionally, the higher the content of CA in CAC, the more obviously the hydration of PC is delayed, confi rming that the CA phase in CAC plays an important role in the delay of PC hydration.

Influence of Cellulose Ethers on Hydration Products of Portland Cement

Cellulose ethers are widely used to mortar formulations,and it is significant to understand the interaction between cellulose ethers and cement pastes.FT-IR spectra,thermal analysis and SEM are used to investigate hydration products in the cement pastes modified by HEMC and HPMC in this article.The results show that the hydration products in modified cement pastes were finally identical with those in the unmodified cement paste,but the major hydration products,such as CH（calcium hydroxide）,ettringite and C-S-H,appeared later in the modified cement pastes than in the unmodified cement paste.The cellulose ethers decrease the outer products and increase inner products of C-S-H gels.Compared to unmodified cement pastes,no new products are found in the modified cement pastes in the present experiment.The HEMC and HPMC investigation shows almost the same influence on the hydration products of Portland cement.

Spectrophotometric Determination of Water-Soluble Hexavalent Chromium and Determination of Total Hexavalent Chromium Content of Portland Cement in the Presence of Iron (III) and Titanium (IV) Using Derivative Ratio Spectrophotometry

A rapid, reliable and accurate method for the determination of hexavalent chromium in Portland cement is developed. The proposed method includes direct spectrophotometric determination of Cr (VI) in Portland cement with 1, 2, 5, 8 Tetrahydroxyanthraquinone, (Quinalizarin, QINZ) at pH 1.5. The European Directive (2003/53/EC) limits the use of cements so that it contains no more than 2 mg.Kg-1 of water-soluble Cr (VI). The absorbance at 565 nm due to Cr (VI)-QINZ complex is recommended for the determination of water-soluble Cr (VI) in Portland cement. The quantification of Cr (VI) released from cement when mixed with water is performed according to TRGS 613 (Technical Rules of Hazardous Substances). The validity of the method is thoroughly examined and the proposed method gives satisfactory results. A derivative spectrophotometric method has been developed for the determination of total Cr (VI) in Portland cement in the presence of Fe (III) and Ti (IV). The hexavalent chromium complex formed at pH 1.5 allows precise and accurate determination of chromium (VI) over the concentration range 0.05 to 3.0 mg.L-1of chromium (VI). The validity of the method was examined by analyzing several Standard Reference Material (SRM) Portland cement samples. The MDL (at 95% confidence level) was found to be 25 ng/mL for chromium (VI) in National Institute of Standards and Technology (NIST) cement samples using the proposed method.

Influence of Benzenediols—Pyrocatechol and Resorcinol—On the Resistance of Portland Cement Mortars with Aluminum Sulfate to Sulfate Attack

The effect of benzene-1,2-diol (pyrocatechol) and benzene-1,3-diol (resorcinol) on the development of sulfate attack in Portland cement mortars containing alkali-free setting accelerator (aluminum sulfate) was studied. It has been found that these compounds (especially pyrocatechol—due to its ability to form chelate complexes with aluminum ions) restrain destructive deformations of Portland cement mortars with aluminum sulfate admixture when under test conditions a constant supply of sulfate ions from external source is provided. According to 27Al-MAS NMR data, pyrocatechol does not influence the amount of ettringite formed in Portland cement paste during its store in sodium sulfate solution. Presumably, in presence of benzenediols, in cement mortars with aluminum sulfate admixture the formation of ettringite crystals with a less pronounced destructive effect takes place.

The Impact of Aluminum- and Iron-Bearing Admixtures on the Resistance of Portland Cement Mortars to Alkali-Silica Reaction and Sulfate Attack

Study of sulfate resistance of mortars with aluminum- and iron-bearing admixtures (Al(OH)3, Al2(SO4)3, FeSO4, Fe2(SO4)3) in conditions close to those established in ASTM C 1012, and the study of the mitigation effect of these admixtures on alkali-silica reaction in accordance with accelerated “mortar bar” test ( GOST 8269.0, ASTM C 1260) were performed. Iron (II) and (III) sulfates show ability for mitigation alkali-silica reaction, while also, in contrast with Al-bearing substances, do not induce the drastic reducing of the initial setting time and do not promote the progress of sulfate corrosion. Compared with FeSO4, iron (III) sulfate has moderate deleterious impact on the early strength of cement paste and can be of interest alone as an inhibitor of ASR. Iron (II) sulfate may be used together with aluminum sulfate to offset the accelerating effect of the latter on the setting of cement paste and to reduce a risk of sulfate corrosion. During prolonged water storage, the mortar elongation and secondary ettringite formation do not occur, even when Al2(SO4)3 is available. Therefore, the investigated admixtures cannot act as agents of internal sulfate attack, however, Al2(SO4)3 can enhance the outer sulfate attack.

The Impact of Aluminum-Containing Set Accelerators on Sulfate Resistance of Portland Cement Compositions

This study contains comparative research of sulfate resistance of ordinary Portland cement pastes with addition of basic aluminum sulfate (hydroxosulfate, Al(OH)1.78(SO4)0.61) and amorphous Al(OH)3. Over 3 months of storing in sodium sulfate solution, the most significant expansion and deterioration occur in case of samples with aluminum hydroxide. During sulfate resistance test, the ratio between aluminum nuclei in AFt (ettringite) and AFm phases was studied by 27Al-MAS NMR, and the impact of aluminum-containing admixtures on this ratio was specified. In accordance with NMR data, in samples with Al(OH)3, the rate of secondary ettringite formation becomes noticeable after one month of storing in sulfate solution. For samples with Al(OH)1.78(SO4)0.61, the rate of elongation and temper of changes in molar ratio between sulfoaluminate phases were comparable with reference samples without admixtures.

Microstructural Evolution Mechanism of C-(A)-S-H Gel in Portland Cement Pastes Affected by Sulfate Ions

The microstructural evolution of C-（A）-S-H gel in Portland cement pastes immersed in pure water and 5.0 wt% Na2SO4 solution for different ages was comparatively investigated, by means of ^（29） Si NMR spectroscopy, and SEM-EDS analysis. Additionally, molecular dynamics simulation was performed to study the aluminum coordination status and interaction of sulfate ions in C-（A）-S-H gel. The results showed significant changes in the microstructural evolution of C-（A）-S-H gel in Portland cement paste. Sulfate attack has decalcifying and dealuminizing effect on C-（A）-S-H gel which is evident from increase in mean chain length（MCL） and decrease in Ca/Si ＆ Al[4]/Si ratios of C-（A）-S-H gel. Additionally, Molecular dynamics simulation proves that Al[4] substituted in silicate chains of C-（A）-S-H gel is thermodynamically metastable, which may explain its migration from the silicate chains and transformation to Al[6], thus lowering the Al[4]/Si ratio of C-（A）-S-H gel. SO4^（2-）ions can carry the interfacial Ca^（2＋） ions into the pore solution by the diffusion-absorption-desorption process, which unravels the mechanism of sulfate attack on C-（A）-S-H gel.