1, 3‐Diethyl‐2‐thiobarbituric acid as an alternative coinitiator for acidic photopolymerizable dental materials. Issue 7 (6th April 2013)
- Record Type:
- Journal Article
- Title:
- 1, 3‐Diethyl‐2‐thiobarbituric acid as an alternative coinitiator for acidic photopolymerizable dental materials. Issue 7 (6th April 2013)
- Main Title:
- 1, 3‐Diethyl‐2‐thiobarbituric acid as an alternative coinitiator for acidic photopolymerizable dental materials
- Authors:
- Münchow, Eliseu A.
Valente, Lisia L.
Peralta, Sonia L.
Fernández, María Raquel
Lima, Giana da S.
Petzhold, Cesar L.
Piva, Evandro
Ogliari, Fabrício A. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The ethyl‐4‐dimethylaminobenzoate (EDAB) is widely used as a coinitiator of the camphorquinone (CQ), but in acidic circumstances it might present some instability, reducing the polymerization efficiency of the material. Considering this, new coinitiators are being evaluated. Hence, this study evaluated the kinetic of polymerization (KP), the degree of conversion (DC), and the rate of polymerization (<italic>R</italic><sub>P</sub>) of experimental resin adhesives containing 1, 3‐diethyl‐2‐thiobarbituric acid (TBA) as a coinitiator of the CQ. The experimental monomeric blend was prepared with bisphenol A glycidyl dimethacrylate, 2‐hydroxyethyl methacrylate, and acidic monomers. CQ was added at 1 mol % as photoinitiator. Six groups were formulated: four containing concentrations of 0.1, 0.5, 1, and 2 mol % of TBA, one without coinitiator, and the last one containing 1 mol % of EDAB (control group). The KP and the <italic>R</italic><sub>P</sub> were performed using real‐time Fourier Transform infrared spectroscopy. The group without coinitiator has not formed a polymer, whereas the addition of TBA resulted in the conversion of monomers in polymer. The DC of the adhesives was as higher as the increase in the TBA content. The group with 2 mol % of TBA presented improved DC and reactivity (<italic>R</italic><sub>P</sub>) than the other groups and the control one. Hence, the TBA has performed as<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The ethyl‐4‐dimethylaminobenzoate (EDAB) is widely used as a coinitiator of the camphorquinone (CQ), but in acidic circumstances it might present some instability, reducing the polymerization efficiency of the material. Considering this, new coinitiators are being evaluated. Hence, this study evaluated the kinetic of polymerization (KP), the degree of conversion (DC), and the rate of polymerization (<italic>R</italic><sub>P</sub>) of experimental resin adhesives containing 1, 3‐diethyl‐2‐thiobarbituric acid (TBA) as a coinitiator of the CQ. The experimental monomeric blend was prepared with bisphenol A glycidyl dimethacrylate, 2‐hydroxyethyl methacrylate, and acidic monomers. CQ was added at 1 mol % as photoinitiator. Six groups were formulated: four containing concentrations of 0.1, 0.5, 1, and 2 mol % of TBA, one without coinitiator, and the last one containing 1 mol % of EDAB (control group). The KP and the <italic>R</italic><sub>P</sub> were performed using real‐time Fourier Transform infrared spectroscopy. The group without coinitiator has not formed a polymer, whereas the addition of TBA resulted in the conversion of monomers in polymer. The DC of the adhesives was as higher as the increase in the TBA content. The group with 2 mol % of TBA presented improved DC and reactivity (<italic>R</italic><sub>P</sub>) than the other groups and the control one. Hence, the TBA has performed as a coinitiator of the CQ for the radical polymerization of methacrylate resin adhesives and it has improved the DC and the reactivity of the materials. Thus, it is a potential coinitiator for the photopolymerization of dental materials. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 101B: 1217–1221, 2013.</p> </abstract> … (more)
- Is Part Of:
- Journal of biomedical materials research. Volume 101:Issue 7(2013:Oct.)
- Journal:
- Journal of biomedical materials research
- Issue:
- Volume 101:Issue 7(2013:Oct.)
- Issue Display:
- Volume 101, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 101
- Issue:
- 7
- Issue Sort Value:
- 2013-0101-0007-0000
- Page Start:
- 1217
- Page End:
- 1221
- Publication Date:
- 2013-04-06
- Subjects:
- Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/jbm.b.32933 ↗
- Languages:
- English
- ISSNs:
- 1552-4973
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.725000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4235.xml