Nawel Matmat , Amir Abdelaziz , Ahmed Fouzi Tarchoun , Hani Boukeciat , Mohammed Jouini , Fateh Chalghoum , Djalal Trache
{"title":"探讨硝酸铵对硝化纤维素-硝化淀粉基复合材料热稳定性和分解动力学的影响","authors":"Nawel Matmat , Amir Abdelaziz , Ahmed Fouzi Tarchoun , Hani Boukeciat , Mohammed Jouini , Fateh Chalghoum , Djalal Trache","doi":"10.1016/j.fpc.2025.01.002","DOIUrl":null,"url":null,"abstract":"<div><div>This study explores a dual-biopolymer-based energetic composite, emphasizing the synergistic effects achieved by combining nitrocellulose (NC) and nitrostarch (NPS) biopolymers with ammonium nitrate (AN), as an oxidizer. The optimal formulation for the AN@NC-NPS composite was determined through theoretical specific impulse (<em>I</em><sub>sp</sub>) calculations using CEA-NASA software. Comprehensive spectral and thermal characterizations were conducted, where FTIR analysis confirmed the effective integration of AN within the NC-NPS matrix, revealing distinctive absorption bands of nitrate esters and AN, indicating a strong chemical compatibility. TGA and DSC analyses demonstrated a two-stage thermolysis, attributed respectively to NC-NPS matrix and AN oxidizer, with a mutual catalytic effect between them, shifting the decomposition process to lower temperatures for both stages. Advanced thermo-kinetic analysis employing various isoconversional approaches enabled precise estimation of key kinetic parameters, including Arrhenius parameters (<em>E</em><sub>a</sub>, Log<sub>10</sub>(<em>A</em>)) and the most probable decomposition mechanisms (<em>g</em>(<em>α</em>), <em>f</em>(<em>α</em>)/<em>f</em>(0.5)). The observed reduction in activation energy across both decomposition stages confirmed the role of AN in enhancing AN@NC-NPS reactivity, further supporting the synergistic catalytic effect revealed by the DSC findings.</div></div>","PeriodicalId":100531,"journal":{"name":"FirePhysChem","volume":"5 4","pages":"Pages 392-402"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exploring the effect of ammonium nitrate on the thermal stability and decomposition kinetics of dual nitrocellulose-nitrostarch-based energetic composites\",\"authors\":\"Nawel Matmat , Amir Abdelaziz , Ahmed Fouzi Tarchoun , Hani Boukeciat , Mohammed Jouini , Fateh Chalghoum , Djalal Trache\",\"doi\":\"10.1016/j.fpc.2025.01.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study explores a dual-biopolymer-based energetic composite, emphasizing the synergistic effects achieved by combining nitrocellulose (NC) and nitrostarch (NPS) biopolymers with ammonium nitrate (AN), as an oxidizer. The optimal formulation for the AN@NC-NPS composite was determined through theoretical specific impulse (<em>I</em><sub>sp</sub>) calculations using CEA-NASA software. Comprehensive spectral and thermal characterizations were conducted, where FTIR analysis confirmed the effective integration of AN within the NC-NPS matrix, revealing distinctive absorption bands of nitrate esters and AN, indicating a strong chemical compatibility. TGA and DSC analyses demonstrated a two-stage thermolysis, attributed respectively to NC-NPS matrix and AN oxidizer, with a mutual catalytic effect between them, shifting the decomposition process to lower temperatures for both stages. Advanced thermo-kinetic analysis employing various isoconversional approaches enabled precise estimation of key kinetic parameters, including Arrhenius parameters (<em>E</em><sub>a</sub>, Log<sub>10</sub>(<em>A</em>)) and the most probable decomposition mechanisms (<em>g</em>(<em>α</em>), <em>f</em>(<em>α</em>)/<em>f</em>(0.5)). The observed reduction in activation energy across both decomposition stages confirmed the role of AN in enhancing AN@NC-NPS reactivity, further supporting the synergistic catalytic effect revealed by the DSC findings.</div></div>\",\"PeriodicalId\":100531,\"journal\":{\"name\":\"FirePhysChem\",\"volume\":\"5 4\",\"pages\":\"Pages 392-402\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FirePhysChem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667134425000021\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FirePhysChem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667134425000021","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Exploring the effect of ammonium nitrate on the thermal stability and decomposition kinetics of dual nitrocellulose-nitrostarch-based energetic composites
This study explores a dual-biopolymer-based energetic composite, emphasizing the synergistic effects achieved by combining nitrocellulose (NC) and nitrostarch (NPS) biopolymers with ammonium nitrate (AN), as an oxidizer. The optimal formulation for the AN@NC-NPS composite was determined through theoretical specific impulse (Isp) calculations using CEA-NASA software. Comprehensive spectral and thermal characterizations were conducted, where FTIR analysis confirmed the effective integration of AN within the NC-NPS matrix, revealing distinctive absorption bands of nitrate esters and AN, indicating a strong chemical compatibility. TGA and DSC analyses demonstrated a two-stage thermolysis, attributed respectively to NC-NPS matrix and AN oxidizer, with a mutual catalytic effect between them, shifting the decomposition process to lower temperatures for both stages. Advanced thermo-kinetic analysis employing various isoconversional approaches enabled precise estimation of key kinetic parameters, including Arrhenius parameters (Ea, Log10(A)) and the most probable decomposition mechanisms (g(α), f(α)/f(0.5)). The observed reduction in activation energy across both decomposition stages confirmed the role of AN in enhancing AN@NC-NPS reactivity, further supporting the synergistic catalytic effect revealed by the DSC findings.