Phase transformations and age-hardening behaviors related to Au3Cu in Au-Cu-Pd alloys. (1/138)

Phase transformation behaviors in Au-Cu-Pd alloys were investigated by means of electrical resistivity measurements, hardness tests, X-ray diffraction and transmission electron microscopy. Anisothermal and isothermal annealing were performed. Two types of phase transformations were found, namely related to the single phase of Au3Cu and the coexistent phase of Au3Cu and AuCu I. The latter produced more remarkable hardening than the former. Hardening was brought about by the antiphase domain size effect of Au3Cu ordered phase in the single phase and by the formation of AuCu I ordered phase in the Au3Cu ordered matrix. There are three modes of phase transformation in the coexistent region depending on the composition. Each sequence is discussed.  (+info)

Reinforcement mechanism of dentin mechanical properties by intracanal medicaments. (2/138)

The reinforcement mechanism of dentin mechanical properties by intracanal medicaments was investigated. The dumbbell-shaped specimens were prepared from a collagen sheet, demineralized dentin and organic dissolved dentin. After immersing the specimens in intracanal medicaments (eugenol and formocresol), the tensile test was carried out in 37 degrees C water and the Vickers hardness test was performed. The tensile strengths increased after eugenol and formocresol immersion, especially collagen and organic dissolved dentin after formocresol immersion and demineralized dentin after eugenol immersion. Thus, formocresol immersion might have reinforced the dentin tensile strength by protein coagulation, while eugenol immersion might have reinforced the dentin tensile strength by not only protein coagulation but also chelation with hydroxyapatite. However, the hardness values did not significantly change after intracanal medicament immersion.  (+info)

Isothermal age-hardening behaviour in a multi-purpose dental casting gold alloy. (3/138)

The isothermal age-hardening behaviour of a multi-purpose dental casting gold alloy was investigated by means of hardness testing, X-ray diffraction study, scanning electron microscopic observations and energy dispersive spectroscopy. By ageing of the solution-treated specimen at 400-500 degrees C, two phases of the Au-rich alpha 1 phase with an f.c.c. structure and the alpha 2 phase with an ordered f.c.c. structure based on Pt3In were transformed into three phases of the alpha 1 phase, the alpha 2 phase and the beta phase with an ordered f.c.t. structure based on PtZn. Hardening was attributed to the fine nodular precipitation resulting from the formation of the beta phase in the alpha 1 matrix. Softening was due to the coarsening of the fine nodular precipitates as the result of consumption of the alpha 2 phase.  (+info)

Isothermal age-hardening behaviour in a Au-1.6 wt% Ti alloy. (4/138)

This study describes research with a view to developing a new age-hardenable, high-carat dental gold alloy with better biocompatibility by addition of a small quantity of titanium to gold. The relationship between isothermal age-hardening and phase transformation of the Au-1.6 wt% Ti alloy was investigated by means of hardness testing, X-ray diffraction study, scanning electron microscopic observation and energy dispersive spectroscopy. The hardening in the initial stage of ageing seemed to be attributable to the continuous precipitation of the Au4Ti ordered phase in the supersaturated alpha solid solution matrix. The overaging with softening was attributed mainly to the formation of precipitates at the grain boundaries, which grew to bright lamellae and seemed to be composed of the Au4Ti phase.  (+info)

High density polyetherurethane foam as a fragmentation and radiographic surrogate for cortical bone. (5/138)

BACKGROUND: Although one of the most important factors in predicting outcome of articular fracture, the comminution of the fracture is only subjectively assessed. To facilitate development of objective, quantitative measures of comminution phenomena, there is need for a bone fragmentation surrogate. METHODS: Laboratory investigation was undertaken to develop and characterize a novel synthetic material capable of emulating the fragmentation and radiographic behavior of human cortical bone. RESULT: Screening tests performed with a drop tower apparatus identified high-density polyetherurethane foam as having suitable fragmentation properties. The material's impact behavior and its quasi-static mechanical properties are here described. Dispersal of barium sulfate (BaSO4) in the resin achieved radio-density closely resembling that of bone, without detectably altering mechanical behavior. The surrogate material's ultimate strength, elastic modulus, and quasi-static toughness are within an order of magnitude of those of mammalian cortical bone. The spectrum of comminution patterns produced by this material when impacted with varying amounts of energy is very comparable to the spectrum of bone fragment comminution seen clinically. CONCLUSIONS: A novel high-density polyetherurethane foam, when subjected to impact loading, sustains comminuted fracture in a manner strikingly similar to cortical bone. Moreover, since the material also can be doped with radio-opacifier so as to closely emulate bone's radiographic signature, it opens many new possibilities for CT-based systematic study of comminution phenomena.  (+info)

The effect of tablet formulation and hardness on in vitro release of cephalexin from Eudragit L100 based extended release tablets. (6/138)

Eighteen batches of cephalexin extended release tablet were prepared by wet granulation method by using Eudragit L100. The effect of the concentration of Eudragit L100, microcrystalline cellulose and tablet hardness on cephalexin release was studied. The formulated tablets were also characterized for physical and chemical parameters. The dissolution results showed that a higher amount of Eudragit in tablet composition and higher tablet hardness resulted in reduced drug release. An increased amount of microcrystalline cellulose in tablet composition resulted in enhanced drug release. Tablet composition of 13.3% w/w Eudragit L100 and 6.6 to 8% w/w microcrystalline cellulose with hardness of 7-11 kg/cm2 gave predicted release for 6 h. The in vitro release was compared with a marketed tablet. Physical and chemical parameters of all formulated tablets were within acceptable limits. The effect of storage on in vitro release and physicochemical parameters of tablets was evaluated and two batches among formulated eighteen batches found to be in acceptable limits.  (+info)

Statistical analysis of tablet breakability methods. (7/138)

PURPOSE: Using a model tablet, the influence of breakability methodology on mass uniformity of half- and quarter-tablets as well as the comparison of different data acquisition and evaluation approaches were investigated. Moreover, different breakability evaluation criteria were compared based upon distribution as well as distribution-free models. METHODS: A cross-scored tablet, i.e. having two break-marks, was broken by different methods by different persons, and the masses determined for the whole (unbroken) tablets, the half-tablets and quarter-tablets. RESULTS: Beside the possible interaction between the methodology and the person breaking the tablets, the major factor significantly influencing the mass uniformity of broken tablets is the breakability methodology. The best results, i.e. smallest loss and smallest variability, are obtained when the breaking force applied by the thumbs is directed towards the score side of the tablet, i.e. by "opening" the score. Using our model tablet, significant differences between the different evaluation criteria are observed, with the USP/NF approach being best in line with the detailed analysis of all broken tablets. CONCLUSIONS: Assuming that for this model tablet the variance is a linear function of the break-line length, the standard deviation of quarter-tablets is theoretically calculated to be 0.87 times the standard deviation of the half-tablets. As the absolute standard deviation, expressed in mass units, will thus remain approximately identical, the relative standard deviation will nearly double as the mean mass of the quarter-tablets will be half of the mean mass of the half-tablets. This was experimentally confirmed.  (+info)

Preparation of antipyretic analgesic by direct compression and its evaluation. (8/138)

Direct compression is able to produce tablets at a lower cost than wet granulation and tableting method, due to a fewer items of process validation. In this study, acetaminophen was used as a medicine with various granular diameters to formulate tablets by direct compression, thus evaluating their physical properties. Consequently, direct compression was found effective in formulating tablets with excellent physical properties, with the granular diameter taken into account. It was confirmed that tablets produced by direct compression were similar in physical properties in tablets produced by wet granulation and tableting method. Further, it was suggested that use of a dry-type binder would make it possible to provide a tablet having higher content of the medicine with excellent physical properties.  (+info)