Study of resin-bonded calcia investment: Part 1. Setting time and compressive strength. (1/25)

This study was carried out to develop a new titanium casting investment consisting of calcia as the refractory material and a cold-curing resin system as the binder. The setting time of the investment was investigated under different N,N-dimethyl-p-toluidine (DMPT) contents in methyl methacrylate monomer (MMA) and benzoyl peroxide (BPO) contents in calcia without any sintering agent. The effects of the sintering agents, which were calcium fluoride (CaF2) and calcium chloride (CaCl2), on the compressive strength of the investments were investigated at room temperature before and after heating to two different temperatures. The shortest setting time (68 minutes) of the investment was obtained at 0.37 DMPT/BPO (1.5 vol% /1.0 mass%) ratio by mass. The highest strength (16.5 MPa) was obtained from the investment which contained 2 mass% CaF2 and was heated to 1,100 degrees C. It was found that the developed calcia investment containing 2 mass% CaF2 has a possibility for use in titanium castings.  (+info)

Study of resin-bonded calcia investment: part 2. Effect of titanium content on the dimensional change of the investment. (2/25)

In the present study, titanium powder was chosen as an expanding agent of an experimentally prepared resin-bonded calcia investment. The effect of Ti content on the dimensional change was investigated. In addition, the effects of the heating rate and heating temperature on the dimensional change of the investment were investigated during setting and after heating. The expansion increased with Ti content and the highest expansion (1.57%+/-0.58) was obtained at 10 mass% Ti. The highest expansion was obtained at 900 degrees C for 30 min heating and was independent of the heating rate. These findings mean that the titanium powder in the calcia investment oxidized sufficiently at that heating condition. It was found that the developed resin-bonded calcia investment was able to compensate for casting shrinkage of pure titanium by adding some Ti powder to the investment.  (+info)

Binding of cations of group IA and IIA to bovine serum amine oxidase: effect on the activity. (3/25)

In this paper, we report on the presence of cation binding areas on bovine serum amine oxidase, where metal ions of the groups IA and IIA, such as Na(+), K(+), Cs(+), Mg(2+), and Ca(2+), bind with various affinities. We found a cation-binding area that influences the enzyme activity if occupied, so that the catalytic reaction may be altered by some physiologically relevant cations, such as Ca(2+) and K(+). This binding area appears to be localized inside the enzyme active site, because some of these cations act as competitive inhibitors when highly charged amines, such as spermine and spermidine, are used as substrates. In particular, dissociation constant values (K(d)) of 23 and 27 mM were measured for Cs(+) and Ca(2+), respectively, using, as substrate, spermine, a polyamine of plasma. An additional cation-binding area, where metal ions such as Cs(+) (K(d) congruent with 0.1 mM) and Na(+) (K(d) congruent with 54 mM) bind without affecting the enzyme activity, was found by NMR.  (+info)

Thermoluminescence in sintered CaF2:Tb. (4/25)

In order to observe and estimate the dose of ultraviolet (UV) radiation, the thermoluminescence (TL) of sintered CaF2 doped with Tb4O7 and Sm2O3 was studied. A several kind of lanthanides elements are doped in pure CaF2 powder crystals and properties of the TL to UV radiation were observed. The TL intensity from CaF2:Tb was the highest among the samples doped other lanthanide elements. The TL emission may be due to the recombination reaction; Tb2+ + hole-->Tb3+*-->Tb3+ + hv. The TL peaks are observed at about 353 K, 378 K and 458 K. It was found that the 378 K TL peak intensity of CaF2:Tb became strong by addition of Sm2O3. The 378 K TL peak may also be suitable for use as a dosimeter.  (+info)

Preparation and properties of nano-sized calcium fluoride for dental applications. (5/25)

OBJECTIVES: The aim of the present study was to prepare nano-sized calcium fluoride (CaF(2)) that could be used as a labile F reservoir for more effective F regimens and as an agent for use in the reduction of dentin permeability. METHODS: Nano-sized CaF(2) powders were prepared using a spray-drying system with a two-liquid nozzle. The properties of the nano-CaF(2) were studied and the effectiveness of a fluoride (F) rinse with nano-CaF(2) as the F source was evaluated. The thermodynamic solubility product of the nano-CaF(2) solution was determined by equilibrating the nanosample in solutions presaturated with respect to macro-CaF(2). Reactivity of the nano-CaF(2) was assessed by its reaction with dicalcium phosphate dehydrate (DCPD). F deposition by 13.2 mmol/L F rinse with the nano-CaF(2) as the F source was determined using a previously published in vitro model. RESULTS: X-ray diffraction (XRD) analysis showed pattern of low crystalline CaF(2). BET measurements showed that the nano-CaF(2) had a surface area of 46.3m(2)/g, corresponding to a particle size of 41nm. Transmission electron microscopy (TEM) examinations indicated that the nano-CaF(2) contained clusters comprising particles of (10-15) nm in size. The nano-CaF(2) displayed much higher solubility and reactivity than its macro-counterpart. The CaF(2) ion activity product (IAP) of the solution in equilibrium with the nano-CaF(2) was (1.52+/-0.05)x10(-10), which was nearly four times greater than the K(sp) (3.9 x 10(-11)) for CaF(2). The reaction of DCPD with nano-CaF(2) resulted in more F-containing apatitic materials compared to the reaction with macro-CaF(2). The F deposition by the nano-CaF(2) rinse was (2.2+/-0.3)mug/cm(2) (n=5), which was significantly (p<0.001) greater than that ((0.31+/-0.06)mug/cm(2)) produced by the NaF solution. SIGNIFICANCE: The nano-CaF(2) can be used as an effective anticaries agent in increasing the labile F concentration in oral fluid and thus enhance the tooth remineralization. It can also be very useful in the treatment for the reduction of dentin permeability.  (+info)

TiF(4) varnish-A (19)F-NMR stability study and enamel reactivity evaluation. (6/25)

The aim of this study was to develop a titanium tetrafluoride (TiF(4)) varnish and evaluate the stability of the formulation and its reactivity with dental enamel. The varnish was prepared in a resinous matrix using ethanol 96% as solvent. Samples (n=45) were aged at 65 degrees C and 30% of relativity humidity (RE n degrees 01/05-ANVISA) and after 3, 6, 9 and 12 months, nine samples were removed for evaluation and compared with fresh samples. Chemical stability of TiF(4) varnish was determinate by (19)F-NMR and the reactivity of the formulation was quantified by formation of fluoride loosely (CaF(2)) and firmly bound (fluorapatite; FA) to enamel. For reactivity comparisons, a varnish without TiF(4) was used as control. The loss of soluble fluoride was about 0.9% after one year of storage. The values of the reactivity (mean+/-S.D.) of fresh, aged at 3, 6, 9 and 12 months and control samples were: CaF(2) (microg F/mm(2)): 89.3+/-27.5(a); 54.5+/-14.3(b); 51.2+/-29.8(b); 69.3+/-21.3(a); 48.0+/-27.4(b); 0.10+/-0.07(c), FA (microg F/g): 2477.5+/-1044.0(a); 2484.8+/-992.0(a); 2580.0+/-1383.9(a); 2517.2+/-929.9(a); 2121.0+/-1059.2(a); 330.0+/-180.0(b), respectively. Means followed by distinct letters were statistically different (p<0.05). After one year of storage, the formulation was chemically stable and the levels of FA were maintained. However there was an initial decrease in the ability to form CaF(2).  (+info)

Effect of a bonding agent on in vitro biochemical activities of remineralizing resin-based calcium phosphate cements. (7/25)

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Anticaries potential of a fluoride mouthrinse evaluated in vitro by validated protocols. (8/25)

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