Application of 4-META on adhesive opaque resin. (Part 1) Adhesive strength and the stability (author's transl)]

Mechanical devices, which has been conventionally used for retaining thermo-setting acrylic resin veneers possesses disadvantage of poor marginal sealing and requires rather complicated procedure applying on the metal casting. An application of adhesive resins to overcome these disadvantages was studied. Adhesive opaque resin consisted of MMA, epoxy acrylate, TiO2 and adhesive monomer 4-META was prepared and the adhesive bonding strength between the opaque resin and Ni-Cr alloy which is for crown and bridge works, was measured. As the results, the opaque resin applied on the metal casting with proper surface treatment showed an excellent adhesive bonding strength of 260 kg/cm2. This value did not decreased even after subjected to 300 time thermal cyclings (4 degrees C and 60 degrees C). After a three months immersion in water at 37 degrees C, adhesive bonding strength decreased slightly to 190 kg/cm2.     

Monomer composition and bond strength of light-cured 4-META opaque resin

A light-cured opaque resin was prepared with 4-(2-methacryloxyethoxycarbonyl) phthalic anhydride (4-META), bifunctional methacrylates, and titanium dioxide (TiO2). The relation between monomer composition and bond strength was examined with seven methacrylate monomers. Methyl methacrylate (MMA) was useful as a solvent of 4-META. However, it was not sufficiently cured by photo-initiator. The bond strength of a triethyleneglycol dimethacrylate (TEGDMA)-based composition was superior to other monomer-based compositions after repeated thermocycles. 1,6-bis(methacryloxy-2-ethoxycarbonyl-amino)-2,4,4-trimethylhex ane (UDMA) effectively provided viscosity to the composition. The prepared opaque resin consisted of 4-META/MMA-TEGDMA primer, TEGDMA-UDMA-based monomer, and titanium dioxide. This opaque resin bonded strongly to alumina-blasted cobalt-chromium alloy. The light-cured 4-META opaque resin may be useful for bonding prosthodontic composite to metal frameworks.     

Studies on Ni-Ta alloys. (Part 2) Age-hardening and metal-to-ceramic bonding (author's transl)]

Age-hardening and metal-to-ceramic bonding were studied on Ni-Ta alloy for dental application. In the first experiment, it was shown the precipitation-hardening was recognized in Ni-33 wt% Ta, Ni-34 wt% Ta except for Ni-30 wt% Ta. The precipitates were of a Widmamst?tten type structure and appeared to be a intermetallic compound, namely Ni3Ta, from the results of X-ray diffraction (debyesherrer) despite of the close proximity of the diffraction patterns of Ni and Ni2Ta. In the second experiment, it was shown that the bonding strength was 176 kg/cm2 for Ni-30 wt% Ta-ceramic system, compared with that of 222 kg/cm2 of Wiron S-ceramic system. The oxide layer was as wide as 3 approximately 5 micron at the Ni-30 wt% Ta-ceramic interface, in which high concentrations of Ni, Ta, and low concentrations of Al, Si were observed. The coefficient of thermal expansion, which was larger than that of porcelain, was 17.4 x 10(-6)/degrees C for Ni-30 wt% Ta.     

Adhesive 4-META/MMA-TBB opaque resin with poly(methyl methacrylate)-coated titanium dioxide

An adhesive opaque resin for veneering on cast metal was developed with 4-methacryloxyethyl trimellitate anhydride and poly (methyl methacrylate)-coated titanium dioxide prepared by aqueous phase polymerization. The opaque resin was a modified 4-META/MMA-TBB resin. The powder consisted of 20% of the encapsulated material and 80% PMMA instead of pure PMMA powder. This resin hides the metal color when the thickness of the resin is as thin as 50 microns. The opaque resin bonded strongly to both cobalt-chromium alloy and visible-light-cured veneering resin. This self-curing opaque resin is applicable not only for bonding veneering resin to an alloy surface but also for bonding fixed partial dentures to enamel surfaces.     

Investigation of Pd-Ag alloy for porcelain fusing. (Part 2) Thermal expansion (author's transl)]

Thermal expansion coefficient and thermal expansion hysteresis (residual expansion after thermal cycles) were measured using nine Pd-Ag alloys (In and/or Sn added) prepared in Part 1. The following results were obtained. (1) The thermal expansion coefficients were ranged 13 approximately 15 x 10(-6)/ degrees C in the temperature range of 400 to 200 degrees C. (2) The effects of the addition of indium and tin to the thermal expansion coefficient depended on the concentration of palladium and silver. (3) The thermal expansion hysteresis was ranged from 0.21 to -0.02% third thermal cycle. It was very small in comparison with that of precious alloys. (4) The thermal expansion hysteresis decreased with increase of addition of indium and tin. (5) The thermal expansion coefficient had no correlation with the bonding strength.     

Adhesion of adhesive resin to dental precious metal alloys. Part II. The relationship between surface structure of Au-In alloys and adhesive ability with 4-META resin

Adhesion of 4-META to Au-In alloy was improved by adding In equivalent to .15% of Au content. On the basis of the results of Au-In alloys analyzed by XPS, the present study investigated the reason why adhesion of the Au-In alloy was improved. The O 1s spectrum could be separated into three oxygen chemical states, In2O3, chemisorbed H2O, and physisorbed H2O. The amount of chemisorbed H2O decreased remarkably with increasing amount of In. It is considered that the poor adhesive ability of the pure gold and alloys containing only small amounts of In was due to the chemisorbed H2O molecules and insufficient indium oxide on the alloy surface. It was established that excellent adhesion requires an oxide with chemical affinity for 4-META to cover at least 50% of the alloy surface.     

Studies of dental methacrylic resin. (Part. 6) Adhesive strength of self-curing methacrylic resin to polymethylmetacrylates with various cross-linking density. (author's transl)]

The adhesive property of dental acrylic resin to resin teeth and denture base resins is an important property, in the case of preperating, repairing and rebasing denture. Then, as models of denture base resin and resin tooth, heat-curing methacrylic resins which were cross-linked with three kinds of polyethylene glycol dimethacrylate, i.e., EDMA, tri-EDMA, nona-EDMA, were prepared, and the tensile adhesive strengths of self-curing methacrylic resin to them were examined. The results were as follows. 1) The tensile adhesive strength under the dry condition was dependent on cross-linking density of adherent resin, and decreased according to the increase of concetration of cross-linking agent added in adherent resin. 2) The greater the number of chain members of cross-linking agent used to adherent resin was, the higher the adhesive strength was. In paticular, the adhesive strength to adherent resin added with nona-EDMA in concentration from 16.7 to 30 mole%, agreed with the tensile strength of adherent resin itself indicating a favourable adhesion. 3) The adhesive strengths under the wet condition, that is, when specimens were immersed in water at 37 degrees C for 21 days, decreased from 30 to 50%, compared with that under the dry condition.     

Aging effect on mechanical properties in fluid resin. (Part 1). Affection of residual monomer (author's transl)]

Aging effect on the mechanical properties in fluid resins was pointed out, but little was studied on this point. Relationship between amount of residual monomer in the samples prepared by fluid resin and the mechanical properties, brinell hardness, tensile strength, were studied. Test pieces just as polymerized in the size were used. Weights of specimens kept at three different circumstances, in the air at 20 degrees C, in a water bath at 37 degrees C and in a desiccator at 11 mmHg and 40 degrees C, was checked at the prescribed time to clarify the amount of residual monomer and the mechanical properties were measured at the same time. Amount of weight loss, due to evaporation of MMA, must improve the mechanical properties. The improvement by postpolymerization could be neglected. Rate of the weight loss suggests that residual monomer must mainly be at the surface. Molecular weight of PMMA, 86.4 X 10(4) did not have any effect on the mechanical properties and on the evaporation rate of monomers from polymerized specimens. To improve the mechanical properties of fluid resin must be to decrease residual monomer as much as possible in the fluid resin especially at the surface area.     

Studies of calcium phosphate glass-ceramics--development of dental materials. (Part 2) Acid resistance--(author's transl)]

It is well known that minerals of bone or tooth are essentially of CaO-P2O5 system. Glass and the crystallized product, i.e., so-called "glass-ceramics" of which chemical composition is 55 CaO . 45 P2O5 (in mole %) and have been developed for biomaterials were subjected to chemical durability test. Human enamel was also tested for the comparison of the data with them. All the specimens were ground to powders in size from 74 to 140 micrometer. A hundred milligram of the powders were immersed into 100 ml. of N/10 acetate buffer (1 mol acetic acid) solution (pH 4.1) at a constant temperature of 37 degrees C. Amount of Ca2+ and P5+ dissolved were determined by an atomic absorption method and Fiske-Subbarow method, respectively. The order of dissolution is human enamel greater than glass greater than glass-ceramics: the amount of Ca2+ (SCa) and P5+ (Sp) with soaking time (t) was expressed by the following equations, :formula: (see book). The glass and the glass-ceramics show good resistance against a weak acid.     

On the polymerization of pour type resin (author's transl)]

The initial polymerization point and the polymerization progress have been observed on powder-liquid pour type acrylic resin and one-liquid pour type acrylic resin. The results are as follows: 1. In case of un-heating at the bottom of powder liquid resin, in the former stage the polymerization makes the regular progress from the bottom part to the upper of the mould, but in the latter stage it does some irregular one. In case of heating at the bottom, at first it shows a better regular progress as in the case of un-heating. 2. In case of un-heating at the bottom of one-liquid resin, in the first stage the polymerization makes the regular progress from the bottom part of the resin and at the same time from its middle of the mould, and then to the upper part and the sprue part. In case of heating at the bottom, it begins just from the heated part, then it goes quite regularly to the middle, the upper, and the sprue part, and lastly the polymerization shrinkage concentrates exclusively at the sprue part.