Effect of polymer on morphology and structure of calcium silicate hydrate prepared via precipitation method

The effects of polyaerylamide （PAM） and polyvinyl alcohol （PVA） on morphology and structure of calcium silica~ hydrate with C/S 1.0-1.7 prepared via precipitation in solution were investigated by XRD, FT-IR and TEM techniques. The results show that incorporation of the polymers decreased the order degree, increased the interlayer spacing and disturbed the layered stacking of C-S-H. Interlayer spacing expansion depended on C/S ratios and type of polymer. Interlayer spacing expansion had a minimum at C/S 1.0 and a maximum at C/S 1.3 and 1.5. Interlayer spacing expansion of PAM was bigger than that of PVA with the same C/S. C-S-H added with PVA mainly exhibited foil-like and fibrillar morphology. The fibrils were of variable length from a few tens of nanometers to a few hundreds of nanometers. Fibrils or foils seemed to be longer in the presence of PVA.     

X-ray diffraction and raman spectroscopy characterization of isotropic pyrocarbon obtained by hot wall chemical vapor deposition

Varying the flow rate of natural gas from 50 to 80 to 120 l/h, isotropic pyrocarbon produced by hot wall chemical vapor deposition at 1000 °C were examined by X-ray diffraction and Raman spectroscopy. The X-ray data were evaluated by Scherrer equation, and the intensity ratio of D to G band derived from Raman data was used to evaluate the lateral extension of isotropic pyrocarbon. The experimental results show that the d ₀₀₂-spacing of isotropic pyrocarbon decreases from 0.3499 nm to 0.3451 nm, while the stack height increases from 6.5 to 8.4 nm with the increase of flow rate of natural gas. The intensity ratio of D to G band and lateral extension of isotropic pyrocarbon increases with natural gas flow rate increasing. After heat treatment, all the crystallite parameters (stack height, lateral extension, and d ₀₀₂-spacing) decrease, indicating the improvement of the arrangement of the basic structural units of isotropic pyrocarbon.     

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.     

Dehydration Characteristics of C-S-H with Ca/Si Ratio 1.0 Prepared Via Precipitation

Calcium silicate hydrate(C-S-H) with Ca/Si ratio 1.0 was prepared via precipitation in solution and heated at various temperatures to investigate its dehydration behavior. The dehydration, structural collapse and recrystallization characteristics of C-S-H and its microstructural change during heating process were investigated by XRD, SEM, Raman and TG-DSC techniques. C-S-H gradually lost non-evaporable water upon heating, about 50% and 80% non-evaporable water was removed below 200 and 400 ℃, respectively, and the rest was removed up to about 1 000 ℃. At 400 ℃, dehydrated C-S-H exhibited the increasing disordering of calcium/silicon environment and the decreasing symmetrical bending vibration of Si-O-Si of Q~2 silicate chains. At 650 ℃ non-bridging oxygen atoms(O_(non)) attached to silicon were almost removed, and significant structural change occurred, and at 815 ℃ C-S-H dehydrated to wollastonite.     

Quantitative calculation of hydration products for binary slag-Portland cement system

The reaction models and the quantitative calculation on the volume fraction of hydration products for binary ground granulated blast-furnace slag （GGBFS） cement system are presented, in which two important factors are taken into account, i e, the reactivity of GGBFS influenced by its chemical compositions and the partial replacement of aluminum phase in calcium silicate hydrate （C-S-H） gel. A simplified treatment is further suggested towards the quantification. In particular, when the replacement level of GGBFS is lower than 70%, the ratio of calcium over silica （C/S） is set at 1.5 or at 1.2 otherwise. The validity of the proposed model is addressed in terms of the contents of calcium Portlandite and non-evaporable water.     

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 products of cement-silica fume-quartz powder mixture under different curing regimes

Composition, morphology, and structure of hydration products in hardened pastes of three kinds of blended cement(cement-silica fume, cement-quartz powder and cement-silica fume-quartz powder) hydrated under different curing regimes(standard curing, 90 ℃ steam curing, 200 ℃ and 250 ℃ autoclave curing) were investigated by X-ray diffraction and field emission scanning electron microscope equipped with EDAX system. Results showed that the main hydration products in three kinds of hardened pastes under standard curing condition are all C-S-H gels, CH, and AFt. Under 90 ℃ steam curing condition, the main hydration products of cement-silica fume and cement-silica fume-quartz powder are C-S-H gels, whereas those of cement-quartz powder are C-S-H and CH. Under 200 or 250 ℃ autoclave curing condition, no obvious crystallized CH phase is found in hardened pastes of three kinds of blended cement, and C-S-H gels are transformed into one or more crystalline phases such as tobermorite, jennite, and xonotlite. The chemical composition and morphology of these crystalline phases depend on the composition of mixture and autoclave temperature.     

Effect of curing regime on polymerization of C-S-H in hardened cement pastes

The effect of two different curing regimes on the polymerization degree of C-S-H in hardened cement pastes within 28 d were investigated by measuring the chemical environments of ²⁹Si with magic angle spinning (MAS) nuclear magnetic resonance (NMR) and by analyzing the ²⁹Si NMR spectra with deconvolution technique. The experimental results indicate that, at curing regime of constant temperature of 20 °C, the polymerization of C-S-H increases and then decreases with curing age, and the Al/Si ratio increases gradually with curing age, furthermore, the two non-bridging oxygen bonds of bridging silicate tetrahedra in C-S-H structure mainly bond to H⁺. At curing regime of variable temperature, the polymerization of C-S-H firstly increases then changes slightly and subsequently decreases with the temperature from low to high and then to low, and the Al/Si ratio firstly increases then keeps invariant and subsequently slightly decreases. Moreover, the temperature decreasing is advantageous for the Ca²⁺ to be bonded to the bridging silicate tetrahedra and entering into the interlayer of C-S-H structure. The polymerization of C-S-H at curing regime of variable temperature is higher than that cured at constant temperature, but the curing regime of constant temperature is more beneficial to the substitution of Al³ for Si⁴⁺ than that of variable temperature.     

Microstructure and flow stress of Mg-12Gd-3Y-0.5Zr magnesium alloy

The microstructure and flow stress of the Mg-12Gd-3Y-0.5Zr magnesium alloy was investigated by compression test at temperatures ranging from 350 to 500 ℃ and the strain rates ranging from 0.01 to 20 s-1. The flow stress of the magnesium alloy increased with strain rate and decreased with deformation temperature. Flow stress can be expressed in terms of the Zener-Hollomon parameter Z, which describes the combined influence of the strain rate and temperature using an Arrhenius function.The values of the deformation activation energy were estimated to be 245.9 and 171.5 kJ/mol at deformation temperatures below 400 ℃ and above 400 ℃, respectively. Two constitutive equations were developed to quantify the effect of the deformation conditions on the flow stress of the magnesium alloy. The effects of deformation temperature and strain rate on the microstructure of the magnesium alloy were also examined and quantified by measuring the volume fraction of dynamically recrystallized grain Xd. Xd increased with increasing of deformation temperature. When the deformation temperature was below 475 ℃, Xd decreased with strain rate until it reached 0.15 s-1, then it increased again. When the deformation temperature was above 475 ℃, Xd increased with strain rate.     

Influence of types and charges of exchangeable cations on ciprofloxacin sorption by montmorillonite

As one of the most important soil components, montmorillonite plays a vital role in transport and retention of organic pollutants in soils. Ciprofloxacin (CIP), an antibiotic of fluoroquiolones, has been frequently detected in water and soil environments due to its wide use in human and veterinary medicine. In this study, the adsorption of CIP onto different homoionic montmorillonite such as Na-, Ca- and Al-MMT was investigated, and the influence of types and charges of exchangeable cations in the interlayer of montmorillonite on CIP adsorption was evaluated. The results showed that different homoionic montmorillonite exhibited different sorption capacity of CIP. At pH 3, the sorption capacity of CIP decreased in the order Na-MMT > Ca-MMT > Al-MMT, following the lyotropic series. When solution pH increased to 11, the sorption capacity of CIP followed the order Ca-MMT > Al-MMT > Na-MMT. Accompanying CIP adsorption on Ca-MMT, a certain amount of Ca2+ was released into solution. Compared to pH 3, the lower Ca concentration in solution at pH 11 indicated that the adsorption of CIP on Ca-MMT at strong alkaline pH was no longer via cation exchange, and surface complexation or cation bridging might contribute to CIP adsorption. The adsorption of CIP on Na- and Ca-MMT at pH 3 and 11 resulted in the expansion of d-spacing, indicative of intercalation of CIP into the interlayer space of the montmorillonite. However, a decrease of d-spacing was observed when CIP adsorbed on Al-MMT at pH 11, which might be attributed to the dissolution of Al-CIP complex formed between CIP and Al3+ in the interlayer of montmorillonite. The results suggest that the types and charges of exchangeable cations in the interlayer of montmorillonite play an important role in CIP adsorption on montmorillonite.     

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…     

Effect of curing regime on the distribution of Al3+ coordination in hardened cement pastes

The effect of curing regime on the distribution of Al³⁺ coordination in hardened cement pastes within 28 d were investigated by ²⁹Si and ²⁷Al magic angle spinning (MAS) nuclear magnetic resonance(NMR) with deconvolution technique. The results indicate that the tetrahedral coordination Al³⁺ incorporated in C-S-H structure mainly originate from the Al³⁺ incorporated in the alite and belite phases in the Portland cement. The curing regime of constant temperature of 20 °C is beneficial to the octahedral coordination Al³⁺ transforming to tetrahedral coordination Al³⁺ incorporated in C-S-H structure. However, at curing regime of variable temperature, the temperature rising process is more advantageous to the transformation from ettringite to monosulphate, substitution of Al³⁺ for Si⁴⁺ in the C-S-H structure and the formation of the third aluminate hydrate (TAH) than that at constant temperature of 20 °C. The high temperature of 60 °C in the holding temperature process promotes the decomposition of ettringite, and enhances the consumption of the Al³⁺ incorporated in C-S-H phases and the Al³⁺ in TAH for the monosulphate forming. The temperature decreasing promotes the transformation from monosulphate to ettringite, and increases the consumption of the Al³⁺ incorporated in C-S-H phases, and then increases the quantity of the TAH.     

不同污泥龄厌氧氨氧化菌的脱氮效能及其动力学特性

为研究不同污泥龄(SRT)条件下厌氧氨氧化菌的脱氮效能和动力学特性,采用一组SBR反应器研究梯度降低污泥龄过程中系统的NO2--N去除负荷(Nr)和NO2--N污泥负荷(Ns),并对各阶段厌氧氨氧化过程动力学特性进行分析.结果表明,污泥龄由21 d梯度降低到12 d,Nr由0.590 kg/(m3·d)降低到0.493 kg/(m3·d),单位MLVSS Ns由0.178 kg/(kg·d)提升到0.297 kg/(kg·d),系统整体的脱氮性能有所下降,但单位质量的厌氧氨氧化菌脱氮效率显著提升;采用莫诺(Monod)模型可以较好地模拟不同污泥龄运行阶段厌氧氨氧化菌的动力学行为,动力学分析表明,随着污泥龄的降低,NO2--N的最大比降解速率vmax由0.406 d-1提高到0.826 d-1,半饱和常数Ks由23.3 mg/L增加到95.3 mg/L,梯度降低污泥龄能够筛选纯化生长速率较快的厌氧氨氧化菌菌种,提升NO2--N的最大比降解速率,但厌氧氨氧化菌对底物的亲和性会逐渐变差,稳定性降低.     

Effect of Curing Regime on Degree of Al3＋ Substituting for Si4＋ in C-S-H Gels of Hardened Portland Cement Pastes

The effect of curing regime on degree of Al3+ substituting for Si4+(Al/Si ratio) in C-S-H gels of hardened Portland cement pastes was investigated by 29Si magic angel spinning(MAS) nuclear magnetic resonance(NMR) with deconvolution technique. The curing regimes included the constant temperature(20, 40, 60 and 80 ℃) and variable temperature(simulated internal temperature of mass concrete with 60 ℃ peak). The results indicate that constant temperature of 20 ℃ is benefi cial to substitution of Al3+ for Si4+, and Al/Si ratio changes to be steady after 180 d. The increase of Al/Si ratio at 40 ℃ is less than that at 20 ℃ for 28 d. The other three regimes of high temperature increase Al/Si ratio only before 3 d, on the contrary to that from 3 to 28 d. However, the 20 ℃ curing stage from 28 to 180 d at variable temperature regime, is benefi cial to the increase of Al/Si ratio which is still lower than that at constant temperature regime of 20 ℃ for the same age. A nonlinear relation exists between the Al/Si ratio and temperature variation or mean chain length(MCL) of C-S-H gels, furthermore, the amount of Al3+ which can occupy the bridging tetrahedra sites in C-S-H structure is insuffi cient in hardened Portland cement pastes.     

Quantum efficiency and temperature coefficients of GaInP/GaAs dual-junction solar cell

GaInP/GaAs dual-junction solar cell with a conversion efficiency of 25.2% has been fabricated using metalorganic chemical vapor deposition(MOCVD) technique.Quantum efficiencies of the solar cell were measured within a temperature range from 25 to 160 ℃.The results indicate that the quantum ef-ficiencies of the subcells increase slightly with the increasing temperature.And red-shift phenomena of absorption limit for all subcells are observed by increasing the cell's work temperature,which are consistent with...     

Effect of CuO on the burnability and mineral formation of high C3S cement clinker

The effect of CuO on the clinkering process and mineral structure, components and morphology of high C3S cement clinker was studied. One reference mixture was prepared according to the potential mineral phase components C3S=75%, C3A=7%, C4AF=18% and then was mixed, respectively, with 0.5%, 1%, 1.5%, 2%, 2.5% and 4% CuO. All samples were heated at a rate of 10°C/min to the design temperatures and then maintained for 40 min. Analyses by the glycerol-ethanol method, XRD and SEM-EDS show that the minimum of free lime (f-CaO) content was related to temperature and CuO amount. The higher the temperature, the lower the amount of CuO corresponding to the f-CaO minimum content. CuO promotes the formation and growth of C3S and C4AF and a new compound is found. In addition, these phenomena are discussed theoretically. In conclusion, CuO alters the burnability and the formation and structure of C3S in a high C3S cement system.     

Effect of intermediate heat treatment temperature on microstructure and notch sensitivity of laser solid formed Inconel 718 superalloy

Inconel 718 superalloys deposited by laser solid forming (LSF) were heat treated with solution treatment,intermediate heat treatment (IHT) and two-stage aging treatment in sequence (SITA heat treatment).The effect of IHT temperature on microstructure,tensile property and notch sensitivity of LSFed Inconel 718 superalloy at 500 ℃ were investigated.As-deposited columnar grains have transformed to equiaxed grains and the grains were refined due to the recrystallization during the SITA heat treatment.It is found that the size and amount of δ phase dispersed at grain boundaries decreased with the increasing of IHT temperature,and δ phase disappeared when the IHT temperature reached 1 020 ℃.The ultimate tensile strength (UTS) and yield strength (YS) of smooth samples increased to a maximum when the IHT temperature reached 980 ℃ and then decreased slightly to a minimum when the IHT temperature was 1 000 ℃,and followed by slight increasing again till the IHT temperature reached 1 020 ℃,resulted from the competition of precipitation strengthening effect of γ″ and γ’ phase and the grain boundary weakening effect caused by the gradual disappearance of δ phase with increasing the IHT temperature.The notch sensitivity factor (qe) decreased but still greater than 1 as the IHT temperature increased,which is attributed to the decrease of the size and amount of δ precipitation.     

Synthesis and characteristics of mesoporous silica aerogels with one-step solvent exchange/surface modification

The synthesis procedures and physical properties of the ambient dried hydrophobic silica aerogels by using different contents of ethanol (EtOH)/trimethylchlorosilane (TMCS)/n-Hexane as surface modification agent were investigated. One-step solvent exchange and surface modification were simultaneously progressed by immersing silica hydrogels in EtOH/TMCS/n-Hexane solution. It is found that microstructures as well as properties of silica aerogels like porosity, specific density and specific surface area are affected by the contents of surface modification agent in the sol from the results of SEM, TEM morphology, FT-IR chemical structure, BET surface area and BJH pore size analyses. The volume of TMCS is of 10% and 20% of hydrogels, and the final product is hydrophilic xerogels. When TMCS’s percent (v/v) is elevated to 75%–100%, hydrophobic silica aerogels with good performance are synthesized, the porosities of aerogels are in the range of 93.5%–95.8% and the average pore size diameter is less than 20 nm. Funded by the National Mega-Project of Scientific & Technical Supporting Programs, Ministry of Science & Technology of China (No.2006BAJ04A 04), and the Science Foundation of Liaoning Province, China (No.20062147)     

Phase structure and electrical properties of La<Subscript>2</Subscript>O<Subscript>3</Subscript>-doped BiInO<Subscript>3</Subscript>-PbTiO<Subscript>3</Subscript> ceramics with high curie temperature

The phase structure and electrical properties of pure and La2O3-doped Bi-InO3-PbTiO3 （BI-PT） ceramics were studied respectively. In （1 -x）BI-xPT （x=0.72-0.80） ceramics, the stability of tetragonal phase increased with increasing x, and pure perovskite structure was obtained for x=-0.80 ceramics. The phase transition temperature range was between 575 ℃ and 600 ℃ for x=0.72-0.80 ceramics, higher than that of PT （-490 ℃）. The c/a ratio almost linearly decreased with increasing La2O3 content in x-0.80 ceramics. It is believed that Pb^2＋ vacancies were formed by La^3＋ substituting Pb^2＋ in La2O3-doped BI-PT ceramics. Tc shifted to lower temperature by 30 ℃/mol% La2O3. The maximum dielectric constant 8557 around 559 ℃ was exhibited in 0.5mol%-doped BI-0.80PT ceramics. La2O3-doped ceramics could be poled resulting from decreasing of c/a ratio and improving of dielectric loss and resistivity. The maximum piezoelectric coefficient d33 was 12 pC/N for 2mol%-doped BI-0.80PT ceramics.     

锚固力在钢筋黏结和端板承压间的分配规律

为获得锚固力在高强热轧钢筋直锚段黏结和端部锚固板承压间的分配规律,以钢筋与混凝土间的黏结-滑移本构关系为基础,利用MATLAB编写出带锚固板钢筋受力计算程序,并通过120个带锚固板钢筋混凝土试件的拉拔试验结果对程序的准确性进行验证.依托程序,分析相对保护层厚度c/d和钢筋屈服强度与混凝土抗拉强度之比fy/ft,对钢筋稳定锚固长度与钢筋公称直径之比las/d的影响以及钢筋屈服强度、混凝土强度等级、混凝土相对保护层厚度、钢筋相对埋置长度等参数对直锚段钢筋黏结应力fb的影响,并拟合得到以fy/ft和c/d为自变量的las/d计算公式.结果表明:las/d随fy/ft的增大而线性增大,随c/d的增大而非线性减小;fb/fy随钢筋埋置长度与稳定锚固长度之比lat/las的变化规律只与混凝土相对保护层厚度有关.继而通过拟合得到加载端钢筋受拉屈服强度时刻,以c/d和lat/las为自变量的fb/fy计算公式.