Open Access. Powered by Scholars. Published by Universities.®

Engineering Commons

Open Access. Powered by Scholars. Published by Universities.®

Articles 1 - 4 of 4

Full-Text Articles in Engineering

Preparation And Testing Of Novel Blocked Isocyanate Dental Adhesives Based Upon Hydroxyhexylmethacrylate, Yunwen Ye Dec 1990

Preparation And Testing Of Novel Blocked Isocyanate Dental Adhesives Based Upon Hydroxyhexylmethacrylate, Yunwen Ye

Theses

A new kind of dental adhesive, O-Chlorophenol-TDI-HEMA-Pentaerythritol (TDI), was studied under long term conditions. The test was done in human third molar teeth which had been extracted 7 days to 6 months. Both citric acid and non citric acid pre-treatments were used on dentin surfaces. Based on Causton's[9] mineralizing solution pre-treatment method, we have used 3 kinds of mineralizing solutions, ITS, 0.5% CaCl2, NaF, as pre-treatment solutions. There were no significant differences between the citric acid and non citric acid pre-treatment. The ITS mineralizing solution pre-treatment caused a large increase in bond strength. The average bond strength of 1791 psi …


Approaches To The Synthesis Of Dentin Bonding Agents Containing Vinyl And Carbamate Functional Groups, Steven W. Amato Sep 1987

Approaches To The Synthesis Of Dentin Bonding Agents Containing Vinyl And Carbamate Functional Groups, Steven W. Amato

Theses

The synthesis of four new monomers containing vinyl and carbamate functional groups was attempted. The desired products were N-m-methacryloxyphenyl-O-phenyl carbamate, N-p-methacryloxy-O-phenyl carbamate, m-N-phenylcarbamato-2-methacryloxyethoxy benzoate, and p-N-phenylcarbamato-2-methacryloxyethoxy benzoate. The carbamate functional group was derived by the Lewis Acid catalyzed reaction of meta-aminophenol, para-aminophenol, meta-aminobenzoic acid, and para-aminobenzoic acid with diphenyl carbonate. The vinyl function was derived, in the case of the aminophenols, by reaction with methacrylyl chloride, and in the case of the aminobenzoic acids, with 2-hydroxyethyl methacrylate.

Partial products only were prepared, these being the two carbamate functional phenols, the two carbamate functional benzoic acids, the two methacryloxy functional derivatives …


Preparation And Properties Of Novel Dental Adhesives Based Upon Pentaerythritol, Yuan-Yuan Su May 1985

Preparation And Properties Of Novel Dental Adhesives Based Upon Pentaerythritol, Yuan-Yuan Su

Theses

Urethane methacrylates were synthesized from Pentaerythritol, TDI, HEMA and four phenolic blocking agents or from hydroxypropyl methacrylatel TDI and two phenolic blocking agents. All the products were characterized by melting pointy infrared spectroscopy, NMR spectra, and elemental analysis. The bonding of these materials to dentin slices was also investigated. Such materials are supposed to not only react with the organic constituent of dentin but also polymerized with restorative resin. It was found that bond strength was enhanced by the use of the urethane methacrylates, resulting in best mean bonding strengths of 2400 psi.


Preparation And Testing Of Blocked Isocyanate Dental Adhesives, George W. Sweitzer May 1985

Preparation And Testing Of Blocked Isocyanate Dental Adhesives, George W. Sweitzer

Theses

Three monomers were used in this study. Two were prepared from 2,4-toluene diisocyanate (TDI),2 hydroxyethyl methacrylate (HEMA), and either o-methoxyphenol, or o-chlorophenol. The third monomer was prepared from pentaerythritol, TDI, HEMA, and p-cresol.

These monomers were bonded to dentin slices, and then combined with an adhesive copolymer consisting of methyl methacrylate and poly(methyl methacrylate). This mixture was polymerized at room temperature by addition of N,N-dimethyl-p-toluidine, and benzoyl peroxide. This adhesive copolymer was applied to monomer coated slices of dentin, and to aluminum coupons already fixed in a jig. The monomer-coated dentin slices (treated with the adhesive copolymer) were then placed …