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1.
Polymers (Basel) ; 13(12)2021 Jun 11.
Artigo em Inglês | MEDLINE | ID: mdl-34208102

RESUMO

This work reports the use of two monomers with two tertiary amines and four methacrylic (TTME) or acrylic (TTAC) terminal groups as co-initiators in the formulation of experimental resin adhesive systems. Both monomers were characterized by FT-IR and 1H NMR spectroscopies. The control adhesive was formulated with BisGMA, TEGDMA, HEMA, and the binary system CQ-EDAB as a photo-initiator system. For the experimental adhesives, the EDAB was completely replaced for the TTME or the TTAC monomers. The adhesives formulated with TTME or TTAC monomers achieved double bond conversion values close to 75%. Regarding the polymerization rate, materials formulated with TTME or TTAC achieved lower values than the material formulated with EDAB, giving them high shelf-life stability. The degree of conversion after shelf simulation was only reduced for the EDAB material. Ultimate tensile strength, translucency parameter, and micro-tensile bond strength to dentin were similar for control and experimental adhesive resins. Due to their characteristics, TTME and TTAC monomers are potentially useful in the formulation of photopolymerizable resins for dental use with high shelf-life stability.

2.
J Mech Behav Biomed Mater ; 110: 103955, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32957247

RESUMO

The objective of this study was to synthesize a diallyl carbonate monomer, allyl(2-(2-(((allyloxy)carbonyl)oxy)benzoyl)-5-methoxyphenyl) carbonate (BZ-AL), and to evaluate its effect as Bis-GMA diluent in the formulation of photopolymerizable dental composite resins. The chemical structure of BZ-AL monomer was determined by means of H1 NMR, C13 NMR and FTIR spectroscopies. An experimental composite comprising a mixture of Bis-GMA and BZ-AL monomers and silanized inorganic filler was formulated. Experimental material was compared with a control composite formulated with Bis-GMA/TEGDMA. Double bond conversion, polymerization kinetics, volumetric shrinkage, polymerization stress, and flexural properties were investigated. The data were analyzed through a Student t-test (α = 0.05). Flexural strength of the experimental materials with BZ-AL monomer showed a statistically significant increase (p < 0.001). The experimental composite has a lower polymerization rate than the control composite, on the other hand, the experimental composite resin has the highest degree of double bond conversion. There are no differences in the polymerization shrinkage of the composites, however, the polymerization stress of the experimental materials was 50% lower than the control resin. Finally, the cell viability test showed that the experimental resins formulated with the BZ-AL monomer was not cytotoxic. Due to its characteristics, BZ-AL monomer is potentially useful for the formulation of composite materials with applications in dentistry.


Assuntos
Metacrilatos , Ácidos Polimetacrílicos , Bis-Fenol A-Glicidil Metacrilato , Carbonatos , Resinas Compostas , Humanos , Teste de Materiais , Polietilenoglicóis , Polimerização
3.
J Mech Behav Biomed Mater ; 104: 103613, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-31929099

RESUMO

Two liquid monomers (CT-AL and CT-ACR) were synthesized from the acylation of tert-butyl catechol with different acid chlorides. The monomers were used to prepare photopolymerizable dental composite for completely replacing TEGDMA. Properties such as flexural strength, modulus of elasticity, degree of double bond conversion, polymerization shrinkage, as well as the polymerization stress were studied. Also, color alteration, translucency, and cytotoxicity were evaluated. The results show that the experimental materials formulated with CT-AL and CT-ACR have similar mechanical properties to a control material formulated with BisGMA/TEGDMA, similar polymerization shrinkage, and less polymerization stress. The composite formulated with the CT-AL monomer shows a similar degree of conversion (72%), while the composite formulated with the CT-ACR monomer has a degree of conversion lower (58%) than the control resin (71%). These results suggest that both monomers could have potential applications in the formulation of composites for dental restorations.


Assuntos
Resinas Compostas , Metacrilatos , Bis-Fenol A-Glicidil Metacrilato , Catecóis , Materiais Dentários , Teste de Materiais , Polietilenoglicóis , Polimerização , Ácidos Polimetacrílicos
4.
Mater Sci Eng C Mater Biol Appl ; 93: 80-87, 2018 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-30274114

RESUMO

This works reports the synthesis and characterization of diallyl(5-(hydroxymethyl)-1,3-phenylene) dicarbonate (HMFBA) and 5-(hydroxymethyl)-1,3-phenylene bis(2-methylacrylate) (HMFBM) monomers and its evaluation as Bis-GMA eluents in the formulation of composite resins for dental use. The experimental materials formulated with HMFBA and HMFBM monomers presented flexural strength values similar to those of the control group formulated with Bis-GMA/TEGDMA. Regarding volumetric contraction percentage, the values obtained of experimental materials with HMFBA was 1.88% and for HMFBM was 4.15%, both lower than control resin (4.68%). In the case of double bond conversion, the resin formulated with HMFBA monomer exhibited a greater degree of conversion (87%). Besides, the DMA analyses proved that the values for Tg guarantee a good mechanical performance at body temperature. The new resins formulated with HMFBA and HMFBM monomers exhibit a cellular viability close to 100%, which indicates the absence of cytotoxicity towards fibroblastic cells.


Assuntos
Resinas Compostas , Fibroblastos/metabolismo , Teste de Materiais , Polietilenoglicóis , Ácidos Polimetacrílicos , Animais , Linhagem Celular , Resinas Compostas/química , Resinas Compostas/farmacologia , Avaliação Pré-Clínica de Medicamentos , Fibroblastos/citologia , Camundongos , Polietilenoglicóis/química , Polietilenoglicóis/farmacologia , Ácidos Polimetacrílicos/química , Ácidos Polimetacrílicos/farmacologia
5.
J Environ Manage ; 177: 65-73, 2016 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-27082258

RESUMO

This work reports the removal of textile dyes and metallic ions by means of adsorption and coagulation-flocculation using two polyelectrolytes and two macroelectrolytes containing sulfonic acid groups. The adsorption of textile dyes was studied in aqueous solutions containing cationic dyes and in wastewater containing a vat dye. Also, removal of vat and naphthol dyes was studied using the process of coagulation-flocculation. The results show these materials possess elevated adsorption capacity, and they accomplished removal rates above 97% in aqueous solutions. The removal of the vat dye improved the quality of the wastewater notably, and an uncolored effluent was obtained at the end of the treatment. The treatment using adsorption decreased the values for coloration, conductivity, suspended solids, and pH. The removal of vat and naphthol dyes by means of coagulation-flocculation was studied as well, and removal rates of 90% were obtained. The polyelectrolytes and macroelectrolytes also proved effective in the adsorption of metallic ions in wastewater. The treatment using adsorption accomplished high removal rates of metallic ions, and it showed greater selectivity towards Cu(2+), Fe(3+) and Pb(2+). A decrease in the content of solids as well as the values for COD and conductivity was observed in the wastewater as well. The analyses of FT-IR indicated that cationic dyes and metallic ions were chemisorbed by means of ionic exchange.


Assuntos
Corantes/química , Polieletrólitos/química , Ácidos Sulfônicos/química , Indústria Têxtil , Águas Residuárias/química , Poluentes Químicos da Água/química , Adsorção , Corantes/análise , Floculação , Concentração de Íons de Hidrogênio , Troca Iônica , Espectroscopia de Infravermelho com Transformada de Fourier , Têxteis , Eliminação de Resíduos Líquidos/métodos , Poluentes Químicos da Água/análise
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