Celine Rose S. Jimenez, Karlo A. Hopia, Kate D. Navor, Amando Allan DM. Bondad, Anniver Ryan P. Lapuz
{"title":"Comparative iso-conversional kinetics of raw and carbonized Dendrocalamus asper (Schult. & Schult.f.) Backer under inert and oxidative atmospheres","authors":"Celine Rose S. Jimenez, Karlo A. Hopia, Kate D. Navor, Amando Allan DM. Bondad, Anniver Ryan P. Lapuz","doi":"10.1016/j.bamboo.2026.100249","DOIUrl":null,"url":null,"abstract":"<div><div>We investigated the biomass fuel characteristics, thermal degradation behaviour and iso-conversional kinetics of raw and carbonized Philippine giant bamboo (<em>Dendrocalamus asper</em>) under inert (N<sub>₂</sub>) and oxidative (air) atmospheres using simultaneous TG–DTG–DSC analyses at heating rates of 5–20 °C min<sup>−1</sup>. Carbonization significantly enhanced fixed carbon content (up to 64.60%), increased gross calorific value (26.96 MJ kg⁻¹) and energy density (4.59 GJ m⁻³), and substantially reduced volatile matter. In nitrogen, raw bamboo exhibited devolatilization within 200–400 °C corresponding to hemicellulose and cellulose degradation, whereas carbonized bamboo showed delayed and broadened high-temperature degradation (300–750 °C) associated with aromatic carbon restructuring. In air, raw bamboo underwent volatile oxidation followed by char combustion, while carbonized bamboo displayed a dominant oxidation stage attributed to char oxidation within 300–650 °C. Iso-conversional analyses using the Ozawa–Flynn–Wall, Starink and Friedman methods revealed conversion-dependent apparent activation energy (<em>E</em><sub>A</sub>) evolution, confirming multi-step kinetics. Under inert conditions, carbonization increased <em>E</em><sub>A</sub> at intermediate to high conversions (<em>α</em> = 0.6–0.8), indicating enhanced structural stability of the condensed carbon matrix. Conversely, in air, carbonized <em>D. asper</em> exhibited markedly lower activation energies (≈42.60–98.64 kJ mol⁻¹) compared to raw bamboo (≈73.21–176.25 kJ mol⁻¹), suggesting a potential mineral-associated catalytic effects supported by Fe<sub>₂</sub>O<sub>₃</sub> enrichment in ash. Overall, carbonization induced an atmosphere-dependent shift in degradation mechanisms, and the validated conversion-dependent kinetic parameters provide intrinsic inputs for mechanistic modeling of bamboo-based biomass energy systems.</div></div>","PeriodicalId":100040,"journal":{"name":"Advances in Bamboo Science","volume":"15 ","pages":"Article 100249"},"PeriodicalIF":3.9000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Bamboo Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773139126000303","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/27 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We investigated the biomass fuel characteristics, thermal degradation behaviour and iso-conversional kinetics of raw and carbonized Philippine giant bamboo (Dendrocalamus asper) under inert (N₂) and oxidative (air) atmospheres using simultaneous TG–DTG–DSC analyses at heating rates of 5–20 °C min−1. Carbonization significantly enhanced fixed carbon content (up to 64.60%), increased gross calorific value (26.96 MJ kg⁻¹) and energy density (4.59 GJ m⁻³), and substantially reduced volatile matter. In nitrogen, raw bamboo exhibited devolatilization within 200–400 °C corresponding to hemicellulose and cellulose degradation, whereas carbonized bamboo showed delayed and broadened high-temperature degradation (300–750 °C) associated with aromatic carbon restructuring. In air, raw bamboo underwent volatile oxidation followed by char combustion, while carbonized bamboo displayed a dominant oxidation stage attributed to char oxidation within 300–650 °C. Iso-conversional analyses using the Ozawa–Flynn–Wall, Starink and Friedman methods revealed conversion-dependent apparent activation energy (EA) evolution, confirming multi-step kinetics. Under inert conditions, carbonization increased EA at intermediate to high conversions (α = 0.6–0.8), indicating enhanced structural stability of the condensed carbon matrix. Conversely, in air, carbonized D. asper exhibited markedly lower activation energies (≈42.60–98.64 kJ mol⁻¹) compared to raw bamboo (≈73.21–176.25 kJ mol⁻¹), suggesting a potential mineral-associated catalytic effects supported by Fe₂O₃ enrichment in ash. Overall, carbonization induced an atmosphere-dependent shift in degradation mechanisms, and the validated conversion-dependent kinetic parameters provide intrinsic inputs for mechanistic modeling of bamboo-based biomass energy systems.