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Setting Time (setting + time)
Selected AbstractsLaboratory strength of glass ionomer and zinc phosphate cementsJOURNAL OF PROSTHODONTICS, Issue 3 2001Andree Piwowarczyk Dr med dent Purpose The present in vitro study examined 3 mechanical properties, namely compressive, flexural, and diametral tensile strength, of various commercially available cements and core materials as a function of time after mixing. Materials and Methods The examined materials were 2 cermet cements (Ketac Silver [ESPE, Seefeld, Germany] and Chelon Silver [ESPE]), 1 metal-reinforced glass ionomer cement (Miracle Mix [GC Dental Industrial Corp, Tokyo, Japan]), 2 conventional glass ionomer cements (Ketac Bond [ESPE] and Ketac Cem [ESPE]), 1 standard cure zinc phosphate cement (Harvard Cement [Richter and Hoffmann, Berlin, Germany]), and 1 zinc phosphate cement with the addition of 30% silver amalgam alloy powder (Harvard Cement 70% with Dispersalloy 30% [Richter and Hoffmann/Johnson and Johnson, East Windsor, NJ]). Properties were measured using a universal testing machine at 15 minutes, 1 hour, and 24 hours after first mixing. Results Compressive strengths varied widely between the 3 times of measurement from 5.8 ± 6.6 MPa for Ketac Cem to 144.3 ± 10.2 MPa for Ketac Silver. Twenty-four hours after mixing, the Bonferroni test showed significant (p, .01) differences between Ketac Silver and all other materials tested. Diametral tensile strengths ranged widely from 4.4 ± 0.9 MPa for Ketac Cem to 11.5 ± 2.2 MPa for Chelon Silver. At 15 minutes, 1 hour, and 24 hours after first mixing, the analysis of variance did not show any significant differences between Ketac Silver, Chelon Silver, and Miracle Mix. The 3-point flexural strength of Ketac Silver showed, at 15 minutes with 13.5 ± 3.9 MPa and at 24 hours with 27.2 ± 7.4 MPa, the highest values. Conclusions Setting time influences the mechanical properties of the materials tested in this study. Ketac Silver, a glass ionomer cement reinforced with sintered glass-silver particles, showed the highest mechanical properties of the examined materials. [source] Examination of cytotoxicity and mutagenicity of AH26 and AH Plus sealersINTERNATIONAL ENDODONTIC JOURNAL, Issue 5 2003I. Mileti Abstract Aim ,To study in vitro the cytotoxic and mutagenic effects of AH26 and AH Plus. Methodology ,Cytotoxic effects on Chinese hamster V79 cells were determined by counting viable cells following incubation with eluations of AH26 and AH Plus. In one set of experiments, the materials were mixed, set for 1 h and then eluted with dimethyl sulphoxide (DMSO) for 1 h, 24 h and 7 days. In the other set, AH26 and AH Plus were mixed and set for 1 h, 24 h and 7 days in physiological saline then crushed and eluted in DMSO for 24 h. The cytotoxic effects of these eluates were evaluated. Three concentrations were chosen to examine the mutagenic effects of AH26 and AH Plus: 5.57, 16.7 and 55.7 ,g mL,1. The structural chromosomal aberration analysis and micronucleus test were performed on human lymphocytes according to standard procedures. Results ,Dose,response curves of cell survival were obtained. Both materials were shown to be cytotoxic in doses larger than 55.7 ,g mL,1, except for AH26, after 7 days setting time. AH Plus was also shown to be toxic in concentrations of 16.7 ,g mL,1, except after 7 days setting time. Neither AH26 nor AH Plus induced a significant increase of chromosomal aberrations or micronuclei induction at any setting time or concentration. Conclusion ,There was no mutagenicity found for AH26 and AH Plus on human lymphocytes in highly controlled conditions in vitro. [source] The influence of the acidic component of the gas-foaming porogen used in preparing an injectable porous calcium phosphate cement on its properties: Acetic acid versus citric acidJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2008Saeed Hesaraki Abstract In the present study, macroporous calcium phosphate cements (CPCs) were prepared using a porogen; that is, the gas-foaming technique. The objective was to investigate the influence of the acidic component of the porogen (acetic acid versus citric acid) on several properties of a specified CPC. In all of the cements prepared, the basic component of the porogen was the same, namely, NaHCO3, and it was added to the powder phase of the cement, while the acidic component of the porogen was dissolved in the liquid phase of the cement. The cements were characterized in terms of initial setting time, porosity, crystallinity, injectability and compressive strength. Also, XRD, FTIR, and SEM techniques were employed to evaluate the phase composition, the chemical groups and the morphological aspects of the porous cements during setting. It was found that the presence of a porogen in a CPC led to significant decreases in both its initial setting time and compressive strength. A CPC made using acetic acid contained a larger amount of the apatite phase but was significantly less injectable and less porous than when citric acid was used. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 [source] Influence of powder particle size distribution on complex viscosity and other properties of acrylic bone cement for vertebroplasty and kyphoplasty,JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2006Lidia Hernández Abstract For use in vertebroplasty and kyphoplasty, an acrylic bone cement should possess many characteristics, such as high radiopacity, low and constant viscosity during its application, low value of the maximum temperature reached during the polymerization process (Tmax), a setting time (tset) that is neither too low nor too high, and high compressive strength. The objective of this study was to investigate the influence of the powder particle distribution on various properties of one acrylic bone cement; namely, residual monomer content, Tmax, tset, complex viscosity, storage and loss moduli, injectability, and quasi-static compressive strength and modulus. It was found that the formulations that possessed the most suitable complex viscosity-versus-mixing time characteristics are those in which the ratio of the large poly(methyl methacrylate) beads (of mean diameter 118.4 ,m) to the small ones (of mean diameter 69.7 ,m) was at least 90% w/w. For these formulations, the values of the other properties determined were acceptable. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006 [source] Characterization of new acrylic bone cements prepared with oleic acid derivativesJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 2 2002Blanca Vázquez Abstract Acrylic bone-cement formulations were prepared with the use of a new tertiary aromatic amine derived from oleic acid, and also by incorporating an acrylic monomer derived from the same acid with the aim of reducing the leaching of toxic residuals and improving mechanical properties. 4-N,N dimethylaminobenzyl oleate (DMAO) was used as an activator in the benzoyl-peroxide radical cold curing of polymethyl methacrylate. Cements that contained DMAO exhibited much lower polymerization exotherm values, ranging between 55 and 62 °C, with a setting time around 16,17 min, depending on the amine/BPO molar ratio of the formulation. On curing a commercial bone cement, Palacos® R with DMAO, a decrease of 20 °C in peak temperature and an increase in setting time of 7 min were obtained, the curing parameters remaining well within limits permitted by the standards. In a second stage, partial substitution of MMA by oleyloxyethyl methacrylate (OMA) in the acrylic formulations was performed, the polymerization being initiated with the DMAO/BPO redox system. These formulations exhibited longer setting times and lower peak temperatures with respect to those based on PMMA. The glass transition temperature of the experimental cements were lower than that of PMMA cement because of the presence of long aliphatic chains of both activator and monomer in the cement matrix. Number average molecular weights of the cured cements were in the range of 1.2×105. PMMA cements cured with DMAO/BPO revealed a significant (p<0.001) increase in the strain to failure and a significant (p<0.001) decrease in Young's modulus in comparison to Palacos® R, whereas ultimate tensile strength remained unchanged. When the monomer OMA was incorporated, low concentrations of OMA provided a significant increase in tensile strength and elastic modulus without impairing the strain to failure. The results demonstrate that the experimental cements based on DMAO and OMA have excellent promise for use as orthopaedic and/or dental grouting materials. © 2002 Wiley Periodicals, Inc. J Biomed Mater Res (Appl Biomater) 63: 88,97, 2002; DOI 10.1002/jbm.10092 [source] Rheological characteristics of suwari and kamaboko gels made of surimi from Indian major carpsJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 9 2002Thazhakot V Sankar Abstract The gel strength, compressibility and folding characteristic of suwari (set) and kamaboko (set and cooked) gels prepared from rohu (Labeo rohita), catla (Catla catla) and mrigal (Cirrhinus mrigala) surimi were examined to understand the occurrence of suwari and modori phenomena in surimi from major freshwater carps. Suwari setting of gels did not take place at lower temperatures. Suwari gels showed good gel strength at 50,°C for rohu and at 60,°C for catla and mrigal after 30,min setting time. Incubation for 60,min decreased the gel strength at 60,°C for rohu and catla. Setting at 25,°C followed by cooking at 90,°C increased the gel strength. Increased setting temperature, however, decreased the gel strength of cooked gels. Gel strength and compressibility data were supported by folding characteristics. © 2002 Society of Chemical Industry [source] Acrylic Bone Cements Modified With Bioactive FillerMACROMOLECULAR SYMPOSIA, Issue 1 2009Carlos Federico Jasso-Gastinel Abstract Bioactive cuttlebone Sepia officinalis particles that contain collagen were used to fill poly (methyl methacrylate- co -styrene) bone cements, varying size and concentration of filler particles. Cuttlebone was characterized by X-ray diffraction and plasma atomic emission spectrophotometer. Maximum reaction temperature and cement setting time were determined for composites and reference (copolymer without filler), along with NMR determination of residual monomer concentration. Mechanical properties characterization included stress-strain, bending, compression, fracture toughness and storage modulus tests. Mechanical results for composites filled with 10 and 30% weight of cuttlebone, complied with norm requirements which opens the possibility for using cuttlebone particles as bioactive filler. [source] A novel silicate-doped calcium-based composite dental pulp capping agentASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 5 2009Fangping Chen Abstract The development of a dental pulp capping agent (DPCA) requires suitable setting time, acceptable compressive strength, favorable bioactivity, and to facilitate cementum tissue regeneration. Calcium phosphate cement (CPC) is widely used for its self-setting, biodegradability, biocompatibility, and formability. However, a relative low strength and lack of bioactivity have limited its application. Herein, dicalcium silicate (Ca2SiO4, C2S) was introduced into CPC to prepare a novel silicate-doped CPC/C2S composite DPCA by self-setting in situ and its setting time, compressive strength, bioactivity, and biomineralization behaviors were investigated. The results indicated that the mechanical strength and setting time of DPCA were higher than those of pure CPC. C2S transformed into a CSH gel without disturbing the hydration of DPCA after soaking in SBF for 5 days. Moreover, much more bone-like hydroxyapatite layers were formed, and DPCA exhibited higher bioactivity mainly in virtue of the rapid formation of CSH. DPCA with 15 wt% C2S, suggested to be the optimized composite, exhibited significantly improved bioactivity and high compressive strength, indicating that DPCA with 15 wt % C2S might have a significant pulp capping therapy advantage over the pure CPC. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source] Injectable acrylic bone cements for vertebroplasty with improved propertiesJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2004Raúl García Carrodeguas Abstract Currently commercially available acrylic bone cements lack adequate radiopacity and viscosity when they are used in percutaneous vertebroplasty (PVP). In this work improved formulations of radiopaque and injectable poly(methyl methacrylate) bone cements were prepared with different amounts (10,50 wt.%) of BaTiO3 or SrTiO3 particles as the radiopaque agent. Two sets of cements were prepared by using untreated or silanated radiopaque particles, respectively. The influence of the content and nature of the radiopaque agent as well as its silanation with 3-(trimethoxysilyl) propyl methacrylate (,-MPS), on the curing parameters, residual monomer content, radiopacity, mechanical properties, and injectability of the resulting materials, was examined. Doughing and setting times, maximum temperature, and compressive strength of all formulations fulfilled the requirements of standard specifications, with values of peak temperature in the range 57,72 °C and those of compressive strength between 114 and 135 MPa. Formulations containing at least 20 wt.% BaTiO3 or SrTiO3 had radiopacities equal to or greater than that corresponding to 2 mm of Al as required for surgical plastics. Injectability of any of the formulations provided 75,80 wt.% of the total mass manually injected through a conventional biopsy needle 4 min after mixing. Silanation of the BaTiO3 or SrTiO3 particles led to formulations with improved mechanical properties and injectability compared to those obtained with the untreated fillers. © 2003 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 68B: 94,104, 2004 [source] Characterization of new acrylic bone cements prepared with oleic acid derivativesJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 2 2002Blanca Vázquez Abstract Acrylic bone-cement formulations were prepared with the use of a new tertiary aromatic amine derived from oleic acid, and also by incorporating an acrylic monomer derived from the same acid with the aim of reducing the leaching of toxic residuals and improving mechanical properties. 4-N,N dimethylaminobenzyl oleate (DMAO) was used as an activator in the benzoyl-peroxide radical cold curing of polymethyl methacrylate. Cements that contained DMAO exhibited much lower polymerization exotherm values, ranging between 55 and 62 °C, with a setting time around 16,17 min, depending on the amine/BPO molar ratio of the formulation. On curing a commercial bone cement, Palacos® R with DMAO, a decrease of 20 °C in peak temperature and an increase in setting time of 7 min were obtained, the curing parameters remaining well within limits permitted by the standards. In a second stage, partial substitution of MMA by oleyloxyethyl methacrylate (OMA) in the acrylic formulations was performed, the polymerization being initiated with the DMAO/BPO redox system. These formulations exhibited longer setting times and lower peak temperatures with respect to those based on PMMA. The glass transition temperature of the experimental cements were lower than that of PMMA cement because of the presence of long aliphatic chains of both activator and monomer in the cement matrix. Number average molecular weights of the cured cements were in the range of 1.2×105. PMMA cements cured with DMAO/BPO revealed a significant (p<0.001) increase in the strain to failure and a significant (p<0.001) decrease in Young's modulus in comparison to Palacos® R, whereas ultimate tensile strength remained unchanged. When the monomer OMA was incorporated, low concentrations of OMA provided a significant increase in tensile strength and elastic modulus without impairing the strain to failure. The results demonstrate that the experimental cements based on DMAO and OMA have excellent promise for use as orthopaedic and/or dental grouting materials. © 2002 Wiley Periodicals, Inc. J Biomed Mater Res (Appl Biomater) 63: 88,97, 2002; DOI 10.1002/jbm.10092 [source] Effects of Saccharide Set Retarders on the Hydration of Ordinary Portland Cement and Pure Tricalcium SilicateJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2010Linghong Zhang The effects of aliphatic sugar alcohols (e.g., threitol, xylitol, sorbitol) on the hydration of tricalcium silicate (C3S) and ordinary portland cement (OPC) were investigated and compared with those of sucrose, a well-established cement set retarder. Only sugar alcohols which contain threo diol functionality retarded the setting of C3S and OPC, their efficacy increasing with the number of threo hydroxy pairs and, to a smaller extent, with the overall population of hydroxy groups. None, however, were as effective as sucrose. The initial and final setting times increased exponentially with the concentration of saccharide, although the hydration of OPC was less inhibited than that of C3S. Saccharides function as "delayed accelerators," that is, cement hydration is first inhibited and then proceeds faster than in saccharide-free cement. This behavior is consistent with the theory that the induction period is controlled by slow formation and/or poisoning of the stable calcium silicate hydrate (CSH) nuclei. The early inhibiting influence of saccharides on CSH precipitation is apparently stronger than on the growth of crystalline calcium hydroxide. Saccharides did not negatively affect the degree of hydration and compressive strength of fully set OPC paste; on the contrary, sorbitol yielded modest increases. [source] Control of Crystallinity of Hydrated Products in a Calcium Phosphate CementJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2009Tao Yu A novel calcium phosphate cement (CPC) was prepared by dry-mechanochemical rout in this work. With the different crystallinity, the CPC showed the different degradation ratio after setting. The degradation ratio of CPC was characterized by the calcium ion-dissolving ratio in deionized water after different soaking time. With the increment of crystallinity, the setting times of CPC were prolonged, and the different mechanical property of CPC were obtained. This novel CPC was supposed to match the new bone ingrowth in vivo and have the potential application in orthopedic surgery for filling non-load-bearing bone defects. [source] Study of two different cold restructuring processes using two different qualities of hake (Merluccius capensis) muscle, with addition of microbial transglutaminaseJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 8 2009Helena M Moreno Abstract BACKGROUND: Microbial transglutaminase (MTGase) can improve the mechanical and functional properties of restructured fish products without the need of thermal gelation. The present study seeks to determine whether, for different setting times, MTGase activity in restructured hake muscle made with pieces or with homogenised muscle can be affected by the quality of the protein in the raw materials. RESULTS: As regards mechanical properties, samples of both qualities subjected to the two different processes attained a suitable consistency after setting for 24 h at 5 °C. The quality of the protein in the sample is important when pieces are used for restructuring, but not when sample is homogenised. Also, there were strong correlations between residual MTGase activity up to 12 h and mechanical properties and electrophoretic band density. Water binding capacity (WBC) was not significantly altered by MTGase addition. CONCLUSION: The experimental combination of 10 g kg,1 of MTGase, 15 g kg,1 of sodium chloride and 7.5 g kg,1 of sodium caseinate was suitable for the production of minimally processed raw restructured fish products made with two different qualities of fish protein and two different restructuring processes. In the restructured products made with pieces, the protein quality significantly affected final properties, but in finely homogenised product the protein quality was less important. Copyright © 2009 Society of Chemical Industry [source] | ||||||||||||||||