Lydia V Ermakova, Ramil R Khasbiullin, Rasim R Saifutyarov, Elizaveta V Ermakova, Petr S Sokolov
{"title":"Thermal Analysis of 1,6-Hexanediol Diacrylate-Based Green Bodies Containing GYAGG:Ce Fabricated by DLP 3D Printing.","authors":"Lydia V Ermakova, Ramil R Khasbiullin, Rasim R Saifutyarov, Elizaveta V Ermakova, Petr S Sokolov","doi":"10.3390/polym18202554","DOIUrl":null,"url":null,"abstract":"<p><p>The thermal decomposition of DLP-printed green bodies containing a cross-linked 1,6-hexanediol diacrylate matrix filled with complex oxide powder of a cerium-activated garnet structure (GYAGG:Ce) was investigated. Non-isothermal thermogravimetric measurements were performed under an argon atmosphere at heating rates of 2, 4, 8 and 20 °C/min (four independent measurements for each heating rate). The main mass-loss stage occurs at approximately 350-470 °C. With the increase in the heating rate, the mean DTG peaks shift to a higher temperature: from 387.1 ± 10.3 °C at 2 °C/min to 427.9 ± 15.2 °C at 20 °C/min. The kinetics of thermal decomposition were investigated using isoconversional analysis methods. The apparent activation energy of the main mass-loss peak calculated by the Kissinger method was 200.85 kJ/mol (R<sup>2</sup> = 0.99). Gas-phase mass-spectrometric analysis tentatively assigned signals to water, CO, CO<sub>2</sub>, and acrylate-derived fragments of organic chains. A thermal analysis-guided debinding schedule was developed and experimentally demonstrated, resulting in the production of bulk ceramics with measurable optical translucence (the full transmittance and in-line transmittance were 54.5% and 12%, respectively, for a sample 1.2 mm thick). The absence of large cracks and delamination was observed in both green and brown bodies by scanning electron microscopy.</p>","PeriodicalId":20416,"journal":{"name":"Polymers","volume":"18 20","pages":""},"PeriodicalIF":5.8000,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13709203/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymers","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.3390/polym18202554","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The thermal decomposition of DLP-printed green bodies containing a cross-linked 1,6-hexanediol diacrylate matrix filled with complex oxide powder of a cerium-activated garnet structure (GYAGG:Ce) was investigated. Non-isothermal thermogravimetric measurements were performed under an argon atmosphere at heating rates of 2, 4, 8 and 20 °C/min (four independent measurements for each heating rate). The main mass-loss stage occurs at approximately 350-470 °C. With the increase in the heating rate, the mean DTG peaks shift to a higher temperature: from 387.1 ± 10.3 °C at 2 °C/min to 427.9 ± 15.2 °C at 20 °C/min. The kinetics of thermal decomposition were investigated using isoconversional analysis methods. The apparent activation energy of the main mass-loss peak calculated by the Kissinger method was 200.85 kJ/mol (R2 = 0.99). Gas-phase mass-spectrometric analysis tentatively assigned signals to water, CO, CO2, and acrylate-derived fragments of organic chains. A thermal analysis-guided debinding schedule was developed and experimentally demonstrated, resulting in the production of bulk ceramics with measurable optical translucence (the full transmittance and in-line transmittance were 54.5% and 12%, respectively, for a sample 1.2 mm thick). The absence of large cracks and delamination was observed in both green and brown bodies by scanning electron microscopy.
期刊介绍:
Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.