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PubMed1996

In vitro investigation of fluoride ion release from four resin-modified glass polyalkenoate cements.

Conventional glass ionomer cements are known to release fluoride ions to the surroundings. Recently, resin-modified glass ionomer cements have been produced. These have differing chemical formulations and this may affect their ability to release fluoride ions. The study evaluates both the fluoride release and compressive strength of one conventional and four resin-modified glass ionomer cements with respect to time. The results showed that the formulation of the resin-modified materials influenced the fluoride release. One resin-modified glass ionomer (PhotacFil) released more fluoride than all other materials, while Vitremer, Fuji II LC and Chemfil Superior release similar amounts. Variglass had a very much smaller elution of fluoride ions. This suggests that there is considerable variation in fluoride release between materials of similar generic origin. The compressive strength of these materials was not affected with time.

Biocompatible Materials↗

PubMed2004

A study of disposed fly ash from landfill to replace Portland cement.

The landfills of fly ash are the problem of all power plants because this disposed fly ash is not used in any work. This research studies the potential of using disposed fly ashes which have disposal time of 6-24 months from the landfill of Mae Moh power plants in Thailand to replace Portland cement type I. Median particle sizes of disposed fly ashes between 55.4 and 99.3 microm were ground to reduce the sizes to about 7.1-8.4 microm. Both original and ground disposed fly ashes were investigated on physical and chemical properties. Compressive strengths of disposed fly ash mortars were determined when Portland cement type I was replaced by disposed fly ashes at the rate of 10%, 20%, and 30% by weight of cementitious material (Portland cement type I and disposed fly ash). The results presented that most particles of original disposed fly ashes were solid and sphere with some irregular shape while those of ground disposed fly ashes were solid and irregular shape. CaO and LOI contents of disposed fly ashes with different disposal times had high variation. The compressive strengths of original disposed fly ash mortars were low but those of ground disposed fly ash mortars at the age of 7 days were higher than 75% of the standard mortar and increased to be higher than 100% after 60 days. From the results, it could be concluded that ground disposed fly ashes were excellent pozzolanic materials and could be used as a partial replacement of cement in concrete, even though they were exposed to the weather for 24 months.

Carbon↗

PubMed1990

Copper-, indium-, tin-, and calcium-fluoride admixed amalgams: release rates and selected properties.

A conventional (Minimax), two single-particle high-Cu (Summalloy and Aristaloy CR), and two dispersed-phase (Cluster and Phasealloy) amalgam alloys were each admixed with 0.5 wt% of CuF2, InF3, SnF2, and CaF2, and evaluated for F-, Cu, and Sn release, as well as for corrosion resistance, microstructure, and compressive strength. Over a 43-week interval, only Cluster revealed somewhat of a sustained F- release in artificial saliva. A ranking for F- release was Cluster (highest), Summalloy, Phasealloy, Minimax, and Aristaloy CR. The effectiveness of the F- compounds in releasing F- followed CuF2 (highest), SnF2, InF3 (1.0%), InF3, and CaF2. Amalgams with admixed CuF2 released both the most Cu and increased Sn. For three amalgams, CaF2 admixtures also increased the Cu release. Constant-potential coulometry distinguished among the different fluoride amalgams. Only Minimax revealed a significant reduction in compressive strength with two admixtures. Microstructural analysis revealed an increased pore distribution around the Ag-Cu dispersed particles, and it was assumed that the F- particles were contained within the pores, since SEM, EDS with a low element detector, and ESCA were all unable to detect the F- particles.

Calcium Fluoride↗

PubMed1997

Effect of crystal seeding on the hydration of calcium phosphate cement.

In this paper, the effect of crystal seeding on the hydration of calcium phosphate cement (CPC) has been carefully investigated. The setting time of the CPC slurry not containing any crystal seeds was 150 min, while the setting time for the specimen containing 5 wt% low crystallinity hydroxyapatite used as a crystal seed was 7 min. This improvement in the setting time was due to HAP serving as a substrate for heterogeneous nucleation which accelerated nucleation. In addition, the compressive strength of the specimen containing the crystal seeding was deduced and we report values different from those previously reported in the literature. The calorimetric curve indicated that crystal seeding could reduce the induction period. A.c. impedance spectroscopy revealed that at the beginning of hydration, the rate of reaction increased and also that the mean diameter and porosity decreased as the seed content increased. At the end of the hydration reaction the situation was changed with the mean diameter and porosity in the sample without any seeds being a minimum, which indicated that the compressive strength was a maximum. This result could be explained by the dissolution and reprecipitation of small hydration products produced by the high rate of reaction produced by the introduction of the crystal seeds.

Journal Article↗

PubMed1988

The effects of a liquid dispersing agent and a microcrystalline additive on the physical properties of type IV gypsum.

This study evaluated the effects of a liquid dispersing agent (LDA) and a microcrystalline additive (MCA) on selected physical properties of type IV gypsum. Working consistency, setting time, setting expansion, and compressive strength (1 hour and 7 days) were determined, following ADA Specification No. 25, on a standard, LDA (0.5, 1, 1.5, and 2 mL), MCA (21.1, 24.1, and 27.1 gm), and combination (LDA 0.75 mL + MCA 12.05 gm) mixes per 300 gm of gypsum. Results indicate that the additives affect the consistency of the mix, but consistency can be kept close to that of the standard by lowering the water/powder ratio. Statistical analysis of the data indicated that the additives significantly affected the setting time, setting expansion, and both the 1-hour and the 7-day compressive strengths. SEM examination of fractured surfaces of test mixes indicated improved crystal packing. The properties of type IV gypsum can be improved by optimizing the amount of LDA and MCA additives.

Calcium Sulfate↗

PubMedDate not supplied

Some physical properties of implant abutment luting cements.

The dislodging force, the compressive strength at 24 hours, and the film thickness of four resin composite luting cements (UDA, UDA with fluoride, Panavia OP, and DenMat) and a conventional glass-ionomer cement (Shofu Type I) were compared. The axial force necessary to dislodge each cemented 0 degree abutment from an internally threaded Steri-Oss implant (n = 5) was then determined using a mechanical testing machine. UDA with fluoride appears to be a significantly stronger luting agent for abutment cementation than is either UDA or DenMat (P less than .05). DenMat resin composite cement exhibited the highest mean compressive strength whereas Panavia OP had the lowest value for film thickness.

Acrylic Resins↗

PubMed2002

Study of a hydraulic dicalcium phosphate dihydrate/calcium oxide-based cement for dental applications.

By mixing CaHPO(4) x 2H(2)O (DCPD) and CaO with water or sodium phosphate buffers as liquid phase, a calcium phosphate cement was obtained. Its physical and mechanical properties, such as compressive strength, initial and final setting times, cohesion time, dough time, swelling time, dimensional and thermal behavior, and injectability were investigated by varying different parameters such as liquid to powder (L/P) ratio (0.35-0.7 ml g(-1)), molar calcium to phosphate (Ca/P) ratio (1.67-2.5) and the pH (4, 7, and 9) and the concentration (0-1 M) of the sodium phosphate buffer. The best results were obtained with the pH 7 sodium phosphate buffer at the concentration of 0.75 M. With this liquid phase, physical and mechanical properties depended on the Ca/P and L/P ratios, varying from 3 to 11 MPa (compressive strength), 6 to 10 min (initial setting time), 11 to 15 min (final setting time), 15 to 30 min (swelling time), 7 to 20 min (time of 100% injectability). The dough or working time was over 16 min. This cement expanded during its setting (1.2-5 % according to Ca/P and L/P ratios); this would allow a tight filling. Given the mechanical and rheological properties of this new DCPD/CaO-based cement, its use as root canal sealing material can be considered as classical calcium hydroxide or ZnO/eugenol-based pastes, without or with a gutta-percha point.

Calcium Compounds↗

PubMed1999

Intravertebral body reconstruction with an injectable in situ-setting carbonated apatite: biomechanical evaluation of a minimally invasive technique.

The ability to mechanically reinforce an osteoporotic vertebral body could impede spinal compression fracture and the associated pain and complications. Previous studies have shown that reinforcement of fractured vertebrae with conventional acrylic cement can relieve symptoms and avoid further collapse. In this study, we explored the use of a carbonated apatite cement combined with a minimally invasive injection technique to improve the compressive mechanical properties of cadaveric vertebral bodies. After establishing the biomechanical characteristics of cement formulations intended to have appropriate viscosities, we evaluated the infiltration of the cements into thoracic vertebral bodies using a combined suction-injection technique. The energy-absorption capabilities of the reinforced vertebral bodies were then measured during axial compressive tests and compared with those of nonreinforced vertebrae. The ultimate compressive strength of the cement formulations averaged from 11.6 to 17.7 MPa, depending on curing conditions. The suction-injection technique allowed from one-half to two-thirds of each vertebral body to be infiltrated with cement. Energy absorption was significantly higher (p < 0.05) between 25 and 70% collapse of the vertebral body in the specimens that received the apatite injection as compared with the controls. These results suggest that osteoporotic vertebral-body augmentation with the injection of apatite cement could prevent further collapse after initial failure has occurred. The osteoconductive nature of the cement and its ability to be remodeled by bone, together with its compressive strength, which is higher than that of cancellous bone, could provide better clinical results than those of current treatments with acrylic cement.

Aged↗

PubMed2002

Leachability of radionuclides from cement-solidified waste form produced at Korean nuclear power plant.

The leach test of radionuclide in cement-solidified waste form was performed. After leach test, compressive strength of waste form was measured. Cement-solidified waste form produced at Korean nuclear power plant, Kori (PWR) was chosen for the leach test. Specimens were cored out from a full-scale waste form (2001 drum size). The leach test procedure used for this study was ANSI/ANS 16.1 procedure. The leach ability indexes for cesium and cobalt isotopes were determined. Semi-infinite model was used for analysis of the controlling mechanism in the release of isotopes. Release mechanism of cesium was dominated by diffusion but release of cobalt behaved somewhat differently from the diffusion controlled release. Averaged leachability indexes were 8.6 for cesium and 11.4 for cobalt. Compressive strength after leach/ immersion test was 7.34 MPa for the sample immersed in simulated seawater and 8.34MPa for the sample immersed in deionized water.

Cesium Radioisotopes↗

PubMed2001

Universal behaviour in compressive failure of brittle materials.

Brittle failure limits the compressive strength of rock and ice when rapidly loaded under low to moderate confinement. Higher confinement or slower loading results in ductile failure once the brittle-ductile transition is crossed. Brittle failure begins when primary cracks initiate and slide, creating wing cracks at their tips. Under little to no confinement, wing cracks extend and link together, splitting the material into slender columns which then fail. Under low to moderate confinement, wing crack growth is restricted and terminal failure is controlled by the localization of damage along a narrow band. Early investigations proposed that localization results from either the linkage of wing cracks or the buckling of microcolumns created between adjacent wing cracks. Observations of compressive failure in ice suggest a mechanism whereby localization initiates owing to the bending-induced failure of slender microcolumns created between sets of secondary cracks emanating from one side of a primary crack. Here we analyse this mechanism, and show that it leads to a closed-form, quantitative model that depends only on independently measurable mechanical parameters. Our model predictions for both the brittle compressive strength and the brittle-ductile transition are consistent with data from a variety of crystalline materials, offering quantitative evidence for universal processes in brittle failure and for the broad applicability of the model.

Journal Article↗

PubMed1999

Mechanical properties of sintered hydroxyapatite and tricalcium phosphate ceramic.

The ultimate values for compressive strength, Young's modulus, and toughness of cylindrical specimens of unitary aspect ratios and uniform grain-size distributions were extrapolated for hydroxyapatite (HAP) to 70 MPa, 9.2 GPa, and 0.36 J cm(-3), and for tricalcium phosphate (TCP), to 315 MPa, 21 GPa, and 2.34 J cm(-3). For total volume porosities of 50%, the corresponding values were determined: for HAP, 9.3 MPa, 1.2 GPa, 0.042 J cm(-3), for TCP, 13 MPa, 1.6 GP, 0.077 J cm(-3). Porosities of HAP specimens ranged from 3%-50%; TCP from 10%-70%. Two pore-size distributions were employed. Exponential dependencies of the mechanical properties were found upon porosity (p < 0.0001). No differences in measured mechanical properties, as determined in compression, could be attributed to pore size. The superiority of TCP increases with density and suggests that a larger or more selective pore-size distribution could be effectively employed in TCP biological implants. This work also suggests the dominant role of secondary calcium phosphates in increasing compressive strengths.

Journal Article↗

PubMed1998

Withdrawal of parathyroid hormone treatment causes rapid resorption of newly formed vertebral cancellous and endocortical bone in old rats.

When administered intermittently, parathyroid hormone (PTH) is a strong anabolic agent, increasing both bone mass and bone mechanical strength and competence. This study evaluates the fate of PTH-induced bone in vertebral bodies after withdrawal of PTH treatment in normal old rats. Sixty-seven 21-month-old male rats were treated with 62 microg/kg/day PTH(1-34) for 8 weeks, followed by saline or bisphosphonate (risedronate, 5 microg/kg twice a week) for another 8 weeks. The rats were scanned by dual-energy X-ray absorptiometry at intervals. The bone mineral content (BMC) of L2-5 increased by 33% during the PTH treatment. The BMC started decreasing shortly after withdrawal of PTH and continued to decline during the 8 weeks after withdrawal of PTH. Risedronate, however, prevented this decrease in BMC. All rats were labeled with tetracycline and calcein 3 weeks and 1 week before the cessation of PTH therapy. In the cancellous bone, PTH increased the mineralized surface: 32.9% +/- 2.8% (mean +/- standard error of the mean) vs. controls 12.0% +/- 1.5%, the mineral appositional rate (0.65 +/- 0.02 to 0.88 +/- 0.06 microm/day), and the cancellous bone volume (BV/TV: 14.5% +/- 0.7% to 27.5% +/- 1.7%). Withdrawal of PTH induced a fast and pronounced bone resorption, decreasing both the extent of the fluorochrome labels and the cancellous bone volume to control values. Risedronate prevented this resorption. In the cortical bone of the vertebral shell, PTH induced large increases in the endocortical mineralized surface, mineral appositional rate, and cortical area. The endocortical fluorochrome labels were, however, resorbed after withdrawal of PTH. Risedronate maintained both the fluorochrome labels and the cortical area. At the periosteum, the response to PTH was less evident, however, and hardly any labeling was seen at the periosteum facing the vertebral canal either in the controls or in the PTH-treated rats. The compressive strength of the vertebral body specimens increased with PTH treatment whether measured in newtons (317 +/- 23 to 623 +/- 54 N), normalized to cross-sectional area (23.0 +/- 1.4 to 44.7 +/- 2.5 N/mm2), or to ash content per millimeter height (58 +/- 2 to 76 +/- 2 N x mm/mg). Withdrawal of PTH decreased the compressive strength and competence to control values. Risedronate, however, maintained the PTH-induced mechanical strength and competence. The study discloses that even in very old rats withdrawal of PTH treatment causes a rapid and pronounced decline in the bone mass deposited during PTH treatment; treatment with risedronate can, however, maintain the PTH-induced bone properties in the axial skeleton of old rats.

Absorptiometry, Photon↗

PubMed1989

[Influence of tannic acid on physical and chemical properties of alpha-tricalcium phosphate-citric acid-tannic acid complex].

A mixture of alpha-tricalcium phosphate [alpha-Ca3(PO4)2; alpha-TCP] with a citric acid solution produces a hardened alpha-TCP-citric acid complex. The influence of tannic acid as an additive in the solution on the physical and chemical properties of the obtained complex was examined as a basic study for new calcium phosphate materials incorporating alpha-TCP. alpha-TCP was mixed with mixing liquids containing citric and tannic acids at various ratios [total acid = 45% (w/w)] at a powder/liquid = 2.2/1.0 (g/g). Compressive strength, setting time, and solubility & disintegration of the resulting complexes were measured by the methods specified by ADAS No. 61. After immersing the plates of the complexes in distilled water for 1 and 7 days, the surface structure of the plates was examined by using X-ray diffraction, scanning electron microscopy and IR spectroscopy. The substances solubilized and disintegrated in the water for 1 day were also examined by measuring quantitative Ca and P concentration. When the ratio of tannic acid to total acids (T/A) was higher than 30% (w/w), both setting time and solubility & disintegration increased remarkably. In the case of the complex at T/A = 30%, both setting time and solubility & disintegration showed the minimum value (6.25 min and 1.70%). For compressive strength, the maximum value (139 MPa) was obtained at T/A = 10%. Although the strength decreased markedly with increasing T/A beyond 10%, that of the complex at T/A = 30% was still a high level (103 MPa). The products on the surfaces before and after immersing the plates in distilled water were also discussed.

Calcium Phosphates↗

PubMed1997

Effect of addition of palladium on properties of Ag2Hg3 (gamma 1) phase.

The effect of palladium addition on the microstructure, compressive strength, creep rate and mercury release rate of Ag2Hg3 (gamma 1) phase was evaluated. Experimental results indicated that fairly pure gamma 1 phase could be fabricated using the present trituration method. The heat treatment of gamma 1 at 90 degrees C increased porosity level, increased dimensional shrinkage, increased mercury vapour release and enhanced the formation of beta1 phase. Addition of palladium in gamma 1 slowed down the amalgamation reaction, largely suppressed the phase transition to beta1 and caused a slight shift in open circuit potential toward the anodic direction. Although the overall anodic polarization profiles did not show a significant effect of palladium, scanning electron microscopy revealed morphological differences between pure and palladium-containing gamma 1. Addition of palladium in gamma 1 also increased compressive strength, increased creep resistance, and largely reduced both mercury vapour and ion release rates. Considering overall performance, the optimal palladium content in gamma 1 seems to be in the range between 0.50 and 0.75 wt%.

Dental Amalgam↗

PubMed1999

Incorporation of a controlled-release glass into a calcium phosphate cement.

A so-called controlled-release glass was synthesized occurring in the system CaO-Na2O-P2O5. A certain sieve fraction of this glass was incorporated in a calcium phosphate cement, of which the powder contained alpha-tricalcium phosphate (alpha-TCP), dicalcium phosphate (DCP) and precipitated hydroxyapatite (HA). The glass appeared to retard the cement setting slightly and it reduced considerably the compressive strength after aging in aqueous solutions which were continuously refreshed. Scanning electron microscope (SEM) pictures and X-ray diffraction (XRD) patterns of the samples after 5 weeks of aging showed that the glass was not dissolved but that large brushite crystals were formed. Thereby, aging in CaCl2 solutions resulted in more brushite formation than aging in NaCl solutions. The brushite crystals did not reinforce the cement. Neither was the aged glass-containing cement weaker than it was before the brushite formation right after complete setting. In conclusion, the incorporation of controlled-release glasses into a calcium phosphate cement and subsequent aging in aqueous solutions did not result in the formation of macropores in the cement structure, but that of brushite crystals. This incorporation reduced the compressive strength of the cement considerably.

Journal Article↗

PubMed2003

[Study on injectable bioactive bone repairing material of nano-hydroxyapatite and polyamide-66 composite].

The aim of this study was to evaluate the injectability, histocompatibility, function and other properties of the injectable bioactive bone repairing material of nano-hydroxyapatite and polyamide-66 (n-HA/PA66) composite. The XRD pattern, the relationship between the injectability and liquid-powder ratio, setting time and liquid-powder ratio, compressive strength and liquid-powder ratio were assessed. The size of the composite was determined to be 70 nm in length and 30 to 50 nm in width, and the molecular weight of polyamides-66 was 18000. The diameter of pores of the composite was about 200 to 400 micrometer. To evaluate the histocompatibility and function, 8 male dogs were studied with the injectable n-HA/PA66 composite implanted in the artificial defected alveolus of mandible on only one side to be compared with the intact alveolus on the other side. The specimens were taken at 4, 8, 12, 16 months after the implantation and the results were evaluated. The XRD pattern of the solidificated n-HA/PA66 composite was the same as the powdered n-HA/PA66 composite. The injectable n-HA/PA66 composite had a good injectability, 25 to 30 minutes setting time and about 37 MPa compressive strength when the liquid-powder ratio was 0.50. The healing of the gingiva was well at the implanted areas in all animals. The height of the repaired alveolar bone was obvious higher than that of the blank control. The earlier sign of ossification was histologically observed at 16 weeks after implantation. The injectable n-HA/PA66 composite has good biocompatibility and osteoconductive property. As an injectable material, with good maneuverability, it is useful for repairing irregular bone defects, especially in oral and maxillofacial surgery.

Alveolar Process↗

PubMed1981

[Studies on the accuracy of the castings. (Part 10) On the effects of starting time of the heat to phosphate bonded investment mold (author's transl)].

Properties of phosphate bonded investments are superior than that of plaster bonded investments in mechanical properties, expansional values for compensating to the casting shrinkage of alloys, and refractory resistance. Therefore, phosphate bonded investments have been available to casting for high fusing alloys. But, their properties are varied easily by manipulating. In this report, two commercial products of Cerami Gold (Whip--Mix Corp.) and Ceravest (G--C Dental Industrial Corp.) were used. They were studied on setting expansion, thermal expansion, compressive strength, change of pH value caused by setting reaction, decrement of weight, casting accuracy and roughness of castings in process of time. Results were follows; 1. The weight decrement of investment mold were about 1.5% on Cerami Gold and 3.5% on Ceravest at 24 hours after the mold had been prepared. 2. pH value of Cerami Gold investment mold changed to 8.5 from 7.0 at 5 hours after mixing, but that of Ceravest investment mold changed to 9.0 from 7.0 at 3 hours. 3. The setting expansion of Cerami Gold investment was caused about 0.9% at 3 hours and that of Ceravest investment was about 0.3% at 1 hour ater mixing. Since then, they were to be constant. 4. The thermal expansion of Cerami Gold investment was decreased by elapsed time until 3 hours after mixing, and then since passing at 5 hours, they were increased. But, that of Ceravest investment was decreased in process of time. 5. The compressive strength of both investments were increased as long as elapsed time after setting. Heating at 800 degrees C in the oven, it was 100--110 Kg/cm2 regardless of time on Ceravest investment, and other was 170 kg/cm2 which was increased until passing 5 hours. 6. The roughness of castings surface were similar to the mold surface and they were H3 12--16 microns which were decreased as elapsed time after investment was mixed. 7. Accurate castings were produced by the mold heated after 24 hours, using with Cerami Gold investment. On the Ceravest investment, it was 30 minutes of 5 hours after mixing.

Dental Casting Investment↗

PubMed2001

[Manufacture and study of porous poly(l-lactic acid) (PLLA)/beta-tricalcium phosphate (beta-TCP) composite].

A promising alternative to supply bone substitutes is to develop living tissue substitutes based on biodegradable materials, which is called bone tissue engineering. One of the research high-lights of bone tissue engineering is to design and manufacture scaffolds for cell attaching, migrating, and proliferating. A process which consists of a solvent casting stage, a compression molding stage and a leaching stage has been used to fabricate macroporous composites of poly(l-lactic acid) (PLLA) and beta-tricalcium phosphate (beta-TCP). The effects of the weight fraction of porogen--NaCl, of the weight ratio of PLLA to beta-TCP and of the diameters of beta-TCP on the porosities, the average pore diameters and the compressive yield strength and compressive modulus have been studied. The results showed that the porosities and the average pore diameters increased and the compressive yield strength and modulus decreased when the weight fraction went from 50% to 90%. The compressive yield strength and compressive modulus could be improved by changing the weight ratio of PLLA to beta-TCP and the diameters of beta-TCP in low-porosity composites (lower than 70%). But high-porosity composites (90%) were not reinforced by changing the weight ratio.

Biocompatible Materials↗