An experimental and theoretical approach on stability towards hydrolysis of triethyl phosphate and its effects on the microstructure of sol-gel-derived bioactive silicate glass

Autor(es)

Bueno, Otto Mao Vargas Machuca ^[1] ; Herrera, Christian Leonardo ^[1] ; Bertran, Celso Aparecido ^[1] ; San-Miguel, Miguel Angel ^[1] ; Lopes, Joao Henrique ^[2]

Afiliação do(s) autor(es)

^[1] Univ Campinas UNICAMP, Dept Phys Chem, Inst Chem, POB 6154, BR-13083970 Campinas, SP - Brazil

^[2] Aeronaut Inst Technol ITA, Dept Chem, Div Fundamental Sci IEF, BR-12228900 Sao Jose Dos Campos, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: Materials Science & Engineering C-Materials for Biological Applications; v. 120, JAN 2021.
• Citações Web of Science: 0

Resumo

The sol-gel method is versatile and one of the well-established synthetic approaches for preparing bioactive glass with improved microstructure. In a successful approach, alkoxide precursors undergo rapid hydrolysis, followed by immediate condensation leading to the formation of three-dimensional gels. On the other hand, a slow kinetics rate for hydrolysis of one or more alkoxide precursors generates a mismatch in the progression of the consecutive reactions of the sol-gel process, which makes it difficult to form homogeneous multicomponent glass products. The amorphous phase separation (APS) into the gel is thermodynamically unstable and tends to transform into a crystalline form during the calcination step of xerogel. In the present study, we report a combined experimental and theoretical method to investigate the stability towards hydrolysis of triethyl phosphate (TEP) and its effects on the mechanism leading to phase separation in 58S bioactive glass obtained via sol-gel route. A multitechnical approach for the experimental characterization combined with calculations of functional density theory (DFT) suggest that TEP should not undergo hydrolysis by water under acidic conditions during the formation of the sol or even in the gel phase. The activation energy barrier (Delta G double dagger) showed a height of about 20 kcal.mol-1 for the three stages of hydrolysis and the reaction rates calculated for each stage of TEP hydrolysis were kFHR = 7.0 x 10(-3)s(-1), kSHR = 6.8 x 10(3)s(-1) and kTHR = 3.5 x 10(3)s(-1). These results show that TEP remains in the non-hydrolyzed form segregated within the xerogel matrix until its thermal decomposition in the calcination step, when P species preferentially associate with calcium ions (labile species) and other phosphate groups present nearby, forming crystalline domains of calcium pyrophosphates permeated by the silicarich glass matrix. Together, our data expand the knowledge about the synthesis by the sol-gel method of bioactive glass and establishes a mechanism that explains the role played by the precursor source of phosphorus (TEP) in the phase separation, an event commonly observed for these biomaterials. (AU)

• Processo FAPESP: 13/07296-2 - CDMF - Centro de Desenvolvimento de Materiais Funcionais
• Beneficiário: Elson Longo da Silva
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs
• Processo FAPESP: 10/05394-9 - Biovidros derivados do 45S5: os efeitos do Nb2O5 ou da modificação da superfície com Ca2+ sobre a estrutura e bioatividade
• Beneficiário: João Henrique Lopes
• Modalidade de apoio: Bolsas no Brasil - Doutorado
• Processo FAPESP: 16/23891-6 - Modelagem computacional da matéria condensada
• Beneficiário: Alex Antonelli
• Modalidade de apoio: Auxílio à Pesquisa - Temático