Effects of molecular structure of polycarboxylate-type superplasticizer on the hydration properties of C3S

Effects of polycarboxylate-type superplasticizer(PC) molecular structure on the hydration heat of tricalcium silicate(C3S) paste and polymerization degree of hydration products(C-S-H gel) were researched by using TAM AIR isothermal microcalorimetry(TA) and 29Si nuclear magnetic resonance(NMR).Methoxy polyethylene glycol-methacrylates-based polycarboxylate superplasticizers with different side chain lengths and main chain lengths were employed.PC molecules with shorter main chain or longer side chains caused stronger retardation of C3S early hydration and lesser increase of C3S 3 d hydration degree.NMR measurement indicated that the incorporation of PC increased the hydration degree of C3S paste and the polymerization degree of silicon-oxygen tetrahedron of C-S-H gel.The tendency for C3S 7 d hydration degree to improve was more pronounced while PC molecules with longer main chain or shorter side chain were added.Whereas,PC molecules with longer main chains or longer side chains increased the 7 d polymerization degree of C-S-H gel.     

Early hydration of composite cement with thermal activated coal gangue

Composite cement samples were prepared by mixing clinker, gypsum with burnt coal gangues which was calcined at various temperatures. The mechanical strength and Ca(OH)₂ content in the cement paste were tested, and the paste composition and microstructure were analyzed by thermogravimetry-differential thermal analysis (TG-DSC), X-ray diffraction(XRD), scanning electronic microscopy (SEM) and pore structure analysis. Results demonstrate that the thermal activated coal gangue could accelerate the early hydration of cement clinker obviously, which promotes the gangue hydration itself. The early hydrated products of the cement are C-S-H gel, Ca(OH)₂ and AFt. The cement with 30% (in mass) the gangue exhibits higher mechanical strength, and among all the cement samples the one with the gangue burnt at 700 °C displays the highest hydration rate, mechanical strength, the most gel pores and the lowest total porosity.     

The hydration characteristics and expansion machanism of expansive cement at low<Emphasis Type="Italic">W/B</Emphasis> ratio

The hydration characteristics and expansion impetus of three kinds of cement paste under free-and confined-curing conditions were investigated, which were respectively mixed with three different kinds of expansive agent at low W/B ratio. The results show that the hydration products of pure cement paste and paste mixed with expansive agent are same, but the amount of hydration products, un-hydrated C₃S and C₂S are obviously different at the same hydration age. At 3 d age, the amount of CH in pure cement paste is less than that of paste mixed with expansive agent, but it is reverse when at 28 d age. The amount of AFt at 3d and 28d age in pure cement paste is less than those of paste mixed with expansive agent. Regardless of under free- or confined-curing condition, the amount of ettringite produced varies little since 3d age. The joint effect of the tumefaction of gel-ettringite due to water absorption and the expansive pressure on the pore caused by the crystalloid ettringite is the cause of the volume expansion of cement paste, and the former effect is much greater than the latter. LU Lin-nu : Born in 1972 Funded by 973 High-tech Project of China (No. 2001CB610704-2) and the Natural Science Foundation of Hubei Province(No. 2002AB075)     

Characterization of pozzolanic reaction and its effect on the C-S-H Gel in fly Ash-cement paste

High resolution solid-state ²⁹Si MAS NMR, combined with XRD, SEM and FTIR were used to characterize the pozzolanic activity of FA, type of main pozzolanic reaction products, and the effect of pozzolanic reaction on the C-S-H microstructure in fly ash-cement (FC) paste. The experimental results indicate that in the hydrated FC paste with 30% dosage of FA at 3 d, FA partially participated in the pozzolanic reaction, while, at 120 d, FA largely reacts. During the hydration of FC paste at laboratory temperature, the pozzolanic reaction products are C-S-H gel rather than zeolitic gel. Moreover, after the covalent bonds of Si-O-Si, Si-O-Al and Al-O-Al in the structure of FA are broken, monosilicates Si-OH and Al-OH groups form, these chemical species can connect C-S-H dimers, thus producing more Al-free C-S-H and aluminous C-S-H than in the plain cement paste. The increased content of Al for Si substitution in the bridging tetrahedra of C-S-H may decrease the stability of C-S-H, which results in a rather obvious loss in the mechanical strength of hardened FC paste.     

Hydration mechanism of sulphoaluminate cement

The feasibility of sulphoaluminate cement (SAC) utilization in support mortar was studied. Setting time and strength of as-received sulphoaluminate cement (SAC) paste were examined, hydration kinetics behavior was determined through Isothermal Calorimeter, and hydration mechanism was investigated by X-Ray diffraction analysis (XRD) and field emission scanning electron microscopy analysis(FSEM). Results showed that as-received SAC contained 61% of anhydrous calcium sulfate (3CA·CaSO4) and dicalcium silicate (C2S). The strength after 1 day or 3 days grew to 68.6% or 85.7% of that after 28 days respectively, while most of hydration heat was released within 1 day. The emergency of three exothermic peaks at acceleration stage was found and hydration kinetics model was established choosing the terminal time of the first exothermic peak at accelerating stage as the beginning of accelerating stage. XRD analysis suggested that large amount of ettringite (AFt) was produced at early age and FSEM observation revealed that ettringite (AFt) formed in sulphoaluminate cement (SAC) paste was characterized of different morphology which was proved to be caused by different ion concentrations.     

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.     

Hydraulicity of Wet-milling Ultra-fine Grouting Cement

The physical and mechanical properties of wet-milling ultra-fine grouting cement were studied,and its microstructure was abserted through modern instrwnentation analysis such as scanning electronic micoscoty (SEM),X-ray diffraction and Hg-intrusion micromeritics ,The experimertal results indicate that wet-milling ultra-fine cement possesses high rheological properties and groutability,It can be filles densely in cracks of rock and hydrate fully,which may endow hydrated cemetnt with high mechanical strength Main hydration products of wetmilling ultra-fine cement are poorly crystalline G-S-H(I),acicular AFt and plank-shape Ca(OH)2,The dense crystal-netwonk structure can be formed in the rock gaps filled with cement psate ,but some weak regions exist owing to Ca(OH)2,The features of micro-pore structure of hydrated wet-milling ultra-fine cement are few big harmful pores,abundant harmless micro pores and little most possible pore radius.     

Effects of clinker contents of different C3A and C4AF on the performance of PSC cement

Phosphogypsum-slag-clink (PSC) cement were prepared by original phosphogypsum(PG), which was grinded after dried at 60 °C combined with different contents of phosphogypsum (15%, 20%, 30%), and a small amount of different C₃A, C₄AF contents of finely ground cement clinker, and ground granulated blast furnace slag (GGBFS). Physical mechanical and sugaring properties were studied. The results show that compressive strength of PSC cement with 20% phosphogypsum at 3 d ages would be higher than 17 MPa and even 50 MPa at 28 days. Compressive strength at longer curing stage and sugaring properties of PSC with lower content of C₃A higher C₄AF clinker were improved. pH value of PSC cement system at early stage was relatively low, and pH gradually increased with the addition of clinker. pH increased firstly and then decreased with the hydration stage. SEM analyses showed that the amount of ettringite, which was influenced by pH and content of Al, must be controlled in PSC cement system, which may cause damage to microstructure or even expansive cracks if large amount of ettringite formed in hardened paste.     

Effects of citric acid on hydration process and mechanical properties of thermal decomposed magnesium oxychloride cement

In order to make full use of salt lake magnesium resources and improve the strength of the thermal decomposed magnesium oxychloride cement(TDMOC), the effects of citric acid on the hydration process and mechanical properties of TDMOC was studied. The hydration heat release at initial 24 h and strengths at 3, 7, and 28 days of TDMOC specimens were conducted. The hydration products and paste microstructure were analyzed by XRD, FT-IR and SEM, respectively. The results showed that citric acid can not only reduce the 24 h hydration heat release and delay the occurring time of second peak of TDMOC, but also produce more 5Mg(OH)2·MgCl 2·8H2O and less Mg(OH)2 in hydration process of TDMOC. More perfect and slender crystals were observed in the microstructure of the TDMOC pastes with citric acid. The results demonstrated that citric acid as an additive of TDMOC can decrease the hydration heat release and increase the compressive strength and flexural strength of TDMOC. The possible mechanism for the strength enhancement was discussed.     

Nanoindentation characteristics of calcium hydroxide-metakaolin blended with sodium hydroxide solutions

In order to determine the active mechanism of metakaolin (MK) as partial replacement of cement in concrete from the nanoscale structure perspective, nanoindentation characteristics of calcium hydroxide (CH)-MK blended with 5 M sodium hydroxide (NaOH) solutions simulating the condition of MK in concrete has been studied. The results indicate that three distinct phases are found by the nanoindentation and BSE tests, such as HD C-S-H gel, LD C-S-H gel and the reaction products with the network structure, the residual unreacted MK and CH, respectively. The volume fraction of HD C-S-H gel is about 96% of all reaction product phases. This means that the use of MK in concrete can increase the volume fraction of HD C-S-H gel and thus will improve the properties of concrete.     

Durability and micro-structure of reactive powder concrete

Durability of traditional reactive powder concrete (RPC) with rich cement and high volume of fly-ash reactive powder concrete (FRPC) were studied. The X-diffraction and scanning electron microscope (SEM) measurement was imployed to analyze the microstructure. The results show that both types of RPC have higher compressive strength, less volume shrinkage ratio and better carbonation-, chloride-, freezing-resistances than the conventional concrete. The results of X-diffraction indicate that they basically have C-S-H as the main composition without Ca(OH)₂ crystal and ettringite. SEM results show that hydration products of FRPC is mainly III-C-S-H which is piled up closely like densely arranged stone body and it has very compacted structure, in addition, Ca/Si ratio of C-S-H gel is lower than 1.5.     

Pore Size Distribution of High Performance Metakaolin Concrete

The Compressive strength, porosity and pore size distribution of high performance metakaolin (MK) concrete were investigated. Concretes containing 0,5%,10% and 20% metakaolin were prepared at a water/cementitious material ratio (W/C) of 0.30.In parallel, concrete mixtures with the replacement of cement by 20% fly ash or 5 and 10% silica fume were prepared for comparison.The specimens were cured in water at 27℃ for 3 to 90 days .The results show that at the early age of curing(3 days and 7 days),metakaolin re-placements increase the compressine strength ,but silica fume replacement slightly reduces the compressine strength.At the age of and after 28 days ,the compressive strength of the concrete with metakaolin and silica fume replace-ment increases.A strong reduction in the total porosity and average pore diameter were observed in the conctete with MK 20% and 10% in the first 7 days.     

Effect of pozzolanic reaction products on alkali-silica reaction

1 IntroductionThe use of fly ashto control the expansion dueto al-kali-silica reaction (ASR) is well established and a num-ber of reviews have been published recently[1-4]. Howflyash brings about this reductionin expansionis not yet un-derstood although a number of theories have been put for-ward to explain its action. For controlling mechanism,they put more emphasis onthe adsorption andresort of al-kali by supplementary cementing material (SCM) , formore acidity oxide in SCM,and the secon…     

Comparison of hydration properties between cement-GGBS-fly ash blended binder and cement-GGBS-steel slag blended binder

The hydration properties of cement-GGBS-fly ash blended binder and cement-GGBS-steel slag blended binder were compared. The experimental results show that the hydration rate of cement-GGBS- steel slag blended binder is higher than that of cement-GGBS-fly ash blended binder within 28 days, but lower than the latter after 28 days. The hydration of cement-GGBS-steel slag blended binder tends to produce more Ca（OH）2 than the hydration of cement-GGBS-fly ash blended binder, especially at late ages. Cement-GGBS- steel slag mortar exhibits higher strength than cement-GGBS-fly ash mortar within 28 days, but at late ages, it exhibits similar compressive strength with eement-GGBS-fly ash mortar and even slightly lower bending strength than cement-GGBS-fly ash mortar. Cement-GGBS-steel slag paste has finer early pore structure but coarser late pore structure than cement-GGBS-fly ash paste. Cement-GGBS-steel slag paste can get satisfied late pore structure and cement-GGBS-steel slag mortar can get satisfied late strength as compared with pure cement paste and pure cement mortar, respectively.     

Influence of CG With High Content of Metallic Particles as a Cement Admixture on Cement Strength

1　IntroductionCopperresidueisanindustrialby productdis chargedbycopperrefineries ,butitusuallycontainssomeusefulmetals .Forexamplecopperresiduecontains 4 %to5 %copper ,1.0 1g tgold ,2 4g tsilverand 4 2 %magne tite ,alltheseexceedthecontentforacomprehensiveutili zation .Inordertoextracttheseusefulmetals ,thecoolingtechnologyofremovingresidueisintroducedbyslowlycooling (4 8h)sothatsomemetallicionsgrow .Afteronemoreflotationforcopperandmagneticbyextractionofiron ,thedischargedresidueiscalledcopp…     

C-S-H cluster microstructure and bonding force investigation base on AFM technology

AFM (atomic force microscopy) technology was applied on C-S-H (calcium silicate hydrate phase) microstructure investigation. The topographies of hydrated C3S (Tricalcium silicate) samples were firstly acquired with AFM. Accordingly, C-S-H can be identified according its pattern. Then the hydrated pssortland cement samples at different curing time were scanned with AFM. The topographies and force displacement curve were acquired and its characters at different days were summarized and analyzed. These results are very meaningful for C-S-H microstructure further investigation and cement-base material macro scale properties improvement.     

Hydration heat effect of cement pastes modified with hydroxypropyl methyl cellulose ether and expanded perlite

Hydration heat effect of cement pastes and mechanism of hydroxypropyl methyl cellulose ether (HPMC) and expanded perlite in cement pastes were studied by means of hydration exothermic rate, hydration heat amount, FTIR and TG-DTG. The results show that HPMC can significantly delay the hydration induction period and acceleration period of cement pastes. As mixing amount increased, hydration induction period of cement pastes enlarged and accelerated period gradually went back. At the same time, the amount of hydration heat gradually decreased. Expanded perlite had worse delay effects and less change of hydration heat amount of cement pastes than HPMC. HPMC changed the structure of C-S-H during cement hydration. The more amount of HPMC, the more obvious effect. However, EXP had little influence on the structure of C-S-H. At the same age, the content of Ca (OH)2 in cement pastes gradually decreased as the mixing amount increase of HPMC and expanded perlite, and had better delay effect than that single-doped with HPMC or expanded perlite when HPMC and expanded perlite were both doped in cement pastes.     

Properties of supersulphated phosphogysumslag cement (SSC) concrete

Supersulphated phosphogysum-slag cement （SSC） is a newly developed non-burned cementitious material mainly composed of phosphogysum （PG） and ground granulated blast furnace slag （GGBFS）, with small amount of steel slag （SS） and clinker （CL）. SSC is a kind of environmentally-friendly cementitious material due to its energy-saving, low-carbon emission, and waste-utilization. We prepared concretes with supersulphated phosphogysum-slag cement, and studied the mechanical properties, micro- properties and resistance to chloride penetration of concrete in comparison with those of portland slag cement （PSC） and ordinary portland cement （OPC） concrete. The test results show that the compressive strength of SSC concrete can reach 38.6 MPa after 28 d, close to PSC concrete and OPC concrete. Microanalyses indicate that large quantities of ettringite and C-S-H, and little amount of Ca（OH）2 are generated during the hydration of SSC. The dense cement paste structure of SSC is formed by ettringite and C-S-H, surrounded unreacted phosphogysum. The property of resistance to chloride penetration of SSC concrete is better than PSC and OPC concrete due to the fact that SSC can form much more ettringite to solidify more Cl^-.     

硅酸盐-硫铝酸盐水泥混合体系的试验研究

研究了不同比例的硅酸盐、硫铝酸盐水泥混合体系的凝结时间、水泥砂浆的强度性能,并对一定混合比例的OPC-SAC水泥进行了XRD、SEM和水化量热测试。结果表明,硅酸盐水泥与硫铝酸盐水泥混合,SAC中的C4A3-S矿物与OPC中的C3S矿物在共同水化过程中有相互促进的作用,会使混合水泥水化和凝结加速;混合水泥的强度性能与两种水泥的混合比例有关。本研究可对硅酸盐-硫铝酸盐水泥混合体系的应用提供借鉴。     

超硫酸盐水泥的水化产物及孔结构特性

采用抗压强度试验、X射线衍射分析、电镜扫描及压汞仪法等测试技术,测试和分析了超硫酸盐水泥在不同龄期的强度、水化产物及孔结构,并将其与普通硅酸盐水泥、矿渣水泥对比,探讨超硫酸盐水泥的水化机理.研究结果表明,超硫酸盐水泥早期强度较低,但后期强度发展快,28 d强度高于42.5普硅水泥;超硫酸盐水泥的主要水化产物为水化硅酸钙、钙矾石及少量石膏晶体,未见普硅水泥及矿渣水泥的主要水化产物氢氧化钙;90 d时,超硫酸盐水泥硬化浆体的阈值孔径、最可几孔径、中孔孔径及平均孔径均小于普硅水泥和矿渣水泥,具有更小的孔隙率和更高的密实度,有效地促进了超硫酸盐水泥后期强度的增长.