Iranian Journal of Materials Science and Engineering

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Abstract: The use of alkali-activated cementitious materials especially over the past decades has significantly been increased. The goal of this research is to investigate the effects of silica modulus and alkali concentration on alkali-activation of blast-furnace slag. In this research, the most important physical characteristics of cementitious systems, i.e. the 28-day compressive strength and final setting time, were studied by changing influencing parameters such as silica modulus, i.e. SiO2/Na2O, (0.44, 0.52, 0.60, and 0.68) and Na2O concentration (4, 6, 8 and 10% by weight of dry binder) at a constant water-to-dry binder ratio of 0.25. Final setting time of the studied systems varies in the range between 55-386 minutes. The obtained results show that systems cured at an atmosphere of more than 95% relative humidity at room temperature exhibit relatively high 28-day compressive strengths up to 107 MPa.

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geopolymer cement (inorganic polymeric binder) based on natural pozzolan are investigated. SiO

of activator and total molar ratios of Nacomposition exhibiting the highest 28-day compressive strength. Mixtures exhibiting the highest compressive strength were studied for their molecular structure using laboratory technique of Fourier transform infrared spectroscopy.Results obtained confirm that changes in chemical composition and curing condition can result in variations in degree of silicon substitution by aluminum in the second coordination sphere. Hydrothermal curing affects the molecular structure so that by increasing the hydrothermal curing temperatures, a lower degree of silicon substitution by aluminum in the second coordination sphere is observed. The molecular structure of the studied inorganic polymeric binde is composed of Si-O-Si chains bonded to Al-O and Si-O units creating two and three dimensional networks.

In this paper, the effects of chemical composition and curing conditions on molecular structure of2/Na2O molar ratio2O/Al2O3, and H2O/Al2O3 were changed to determine the optimum chemical

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Abstract: SiC nano particles with mono dispersed distribution were synthesized by using of silicon alkoxides and phenolic resin as starting materials. After synthesis of sample, characterizations of the obtained powder were investigated via Fourier Transform Infrared Spectroscopy (FTIR) with 400-4000 cm-1, X-ray Diffractometry (XRD), Laser Particle Size Analyzing (LPSA), Si29 NMR analysis, Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). FTIR and Si29 NMR results of the gel powder indicated that Si-O-C bonds were formed due to hydrolysis and condensation reactions . FTIR results showed a very strong peak for heat treated powder at 1500°C after carbon removal which is corresponded to Si-C bond. Obtained pattern from X-ray diffractometry showed that the final products contain -SiC phase with poly crystalline planes and little amounts of residual carbon. PSA results showed that the average particles size were 50.6 nm with monosized distribution. Also microstructural studies showed that the SiC nano powders have semi spherical morphology with mean particles size of 30-50 nm and also there are some agglomerates with irregular shape.

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Shrinkage behavior of a geopolymer cement paste prepared from pumice-type natural pozzolan was studied
by changing parameters of chemical composition including SiO2/Na2O molar ratio of activator and total molar ratios
of Na2O/Al2O3, and H2O/Al2O3. For investigating the effect of curing conditions on shrinkage, hydrothermal curing
was also applied. The obtained results clearly revealed the governing effect of chemical composition on shrinkage.
Mixes with different Na2O/Al2O3 molar ratios exhibited different shrinkage behavior due to variations made in
SiO2/Na2O molar ratio. Application of hydrothermal curing after a 7-day period of precuring in humid atmosphere
also showed strong effect on shrinkage reduction.

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Abstract: The linear expansion, early-age compressive strength and setting times of the binary mixtures of gypsum and Portland cement clinkers of relatively low C3A-contents were investigated. For this reason, type 1, 2, and 5 of Portland cement-clinkers were selected and a number of binary mixtures were designed. At relatively lower percentages of gypsum (about 5%), the early strength behavior is improved. Results obtained for compressive strength of mixtures with 5% gypsum confirm the possibility of achieving 28- and 90-day compressive strengths up to values higher than 100 MPa and 130 MPa, respectively. At relatively higher percentages of gypsum (more than 25%), excessive expansion caused by ettringite formation results in the formation of micro-cracks effectively weakening the strength behavior. The work suggests that type S expansive cements could be produced from Portland cement clinkers of relatively low C3Acontents.

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Mono dispersed nano SiC particles with spherical morphology were synthesized in this project by hydrolysis and condensation mechanism during sol gel processing. pH, temperature and precursor’s ratio considered as the main parameters which could influence particles size. According to DLS test results, the smallest size of particles in the sol (<5nm) was obtained at pH<4. It can be observed from rheology test results optimum temperature for achieving nanometeric gel is about 60 ˚C. The optimum pH values for sol stabilization was (2-5) determined by zeta potentiometery. Si 29NMR analysis was used in order to get more details on final structure of gel powders resulted from initial sol. X-ray diffraction studies showed sythesized powder consists of β-SiC phase. Scanning electron microscopy indicated agglomerates size in β-SiC synthesis is less than 100 nm. Finally, TEM studies revealed morphology of β-SiC particles treated in 1500˚C and after 1hr aging is spherical with (20-30) nm size

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This article addresses the interplay between heat of hydration and physico-mechanical properties of calcium sulfate hemi-hydrate in the presence of retarding additives such as citric and malic acids and sodium citrate. The heat of hydration was measured using a semi-isothermal calorimeter. Results proved that citric and malic acids had superior impact on hydration and mechanical properties. While the concentration of additives was increasing, the maximum heat of hydration was decreasing from 56.15 cal/g.min for blank sample to 33 cal/g.min for high concentrations of citric and malic acids. Consequently, the measured time to this maximum heat of hydration and thus the induction period were increased significantly from 5 to 105 min. Mechanical results indicated that the increase in the amounts of additive led to the reduction of the compressive strength from 16.25 MPa in the blank sample up to 74% for the highest concentration of malic acid

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Quaternary ammonium compounds (QACs) are among the most commonly used antibacterial agents. The aim of this study was to synthesize a dimethacrylate monomer functionalized with a QAC and to study its effect on the properties of an orthodontic adhesive primer. Urethane dimethacrylate monomer functionalized with a QAC (UDMAQAC) was synthesized and then characterized by nuclear magnetic resonance spectroscopy (NMR) and Fourier transform infrared spectroscopy (FTIR). 5, 10, 15 and 20 wt% of UDMAQAC was added to an orthodontic adhesive primer (control group). FTIR analysis was used to measure the degree of conversion (DC). The bond strength of dental brackets was measured by shear bond strength (SBS) test and adhesive remaining index (ARI) was evaluated by stereomicroscope. Agar diffusion test and MTT assay were used to evaluate the antibacterial property and cell viability, respectively. Statistical analysis included one-way ANOVA with Tukey’s post hoc test and Kruskal-Wallis nonparametric test (P˂0.05). Although the obtained data did not show significant differences between the SBS and DC of different groups, but the highest values were obtained by adding 10 wt% monomer. Adding more than 10 wt% UDMAQAC resulted in significant increase in antibacterial property. The 15 and 20 wt% groups showed significantly lower cell viability

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Amorphous calcium phosphate (ACP) which is a transient phase in natural bio-mineralization process has recently gained the spotlight. This study aimed to assess the effect of incorporation of nano-ACP (NACP) in a dental adhesive with/without surface treatment with silane coupling agent on bond strength. NACP was synthesized by the wet chemical precipitation technique. To characterize the structure of NACP, X-ray diffraction, scanning electron microscopy and energy dispersive X-ray spectroscopy were used. Forty molars were randomized into 4 groups of 10. The teeth were restored with composite resin and the bonding agent (one of the four groups). Adper Single Bond 2 was used as the control group. In 4wt% NACP group, NACP fillers were added to the bonding agent. In 0.4wt% and 4wt% SNACP groups, silanized NACP fillers were added to the bonding agent. Finally, the mode of failure of specimens was determined. Data were analyzed by one-way ANOVA and Tukey's post-hoc tests. P<0.05 was considered statistically significant. Addition of 4wt% non-silanized NACP decreased the bond strength compared with the control group (P<0.05). The bond strength of the groups with silanized fillers was not significantly different from that of the control group. Addition of silanized NACP to dental adhesive had no significant adverse effect on bond strength, which is a promising finding to pave the way for the synthesis of bonding agents containing bioactive fillers.