Bio-Based Hydroxypropyl Methylcellulose Reinforced Water Glass/Silica Sol Hybrid Gel Foam with Synergistic Flame-Retardant and Enhanced Fireproof Performance Under Laboratory Screening Conditions for Forest Fire Barriers.
Saved in:
| Title: | Bio-Based Hydroxypropyl Methylcellulose Reinforced Water Glass/Silica Sol Hybrid Gel Foam with Synergistic Flame-Retardant and Enhanced Fireproof Performance Under Laboratory Screening Conditions for Forest Fire Barriers. |
|---|---|
| Authors: | Wang, Pengfei1 (AUTHOR) crx41927294@163.com, Bai, Zhiming2 (AUTHOR) wangpengfei@tfri.com.cn, Cong, Ruoxin2,3 (AUTHOR), Yang, Hongyu1,3 (AUTHOR) yhongyu@cqu.edu.cn |
| Source: | Materials (1996-1944). Jun2026, Vol. 19 Issue 12, p2434. 23p. |
| Subjects: | Forest fire prevention & control, Fireproofing agents, Thermal stability, Foam, Silica, Soluble glass, Cellulose |
| Abstract: | Highlights: A composite of water glass/HPMC/silica sol (SGF-HPMC-SOL) was constructed. A stable organic–inorganic hybrid network enhances the material's properties. Its flame-retardant performance is superior to that of traditional gels. To meet the requirements of forest fire prevention, a water glass-based composite gel foam was developed by introducing hydroxypropyl methylcellulose (HPMC) and nanosilica sol into a sodium silicate/sodium bicarbonate matrix. The resulting water glass/HPMC/silica sol ternary system (SGF-HPMC-SOL) was designed to improve water retention, foam stability, substrate adhesion, and fire-barrier durability. The results indicate that HPMC and silica sol contributed to network reinforcement through hydrogen bonding, polymer-chain entanglement, nanoscale filling, and possible interfacial condensation. The optimized SGF-HPMC-SOL retained 20.4% of its initial mass after heating at 100 °C for 5 h, compared with 4.65% for SGF and 9.54% for SGF-HPMC; reached a carbonization time of 164 s under direct-flame exposure, versus 100 s for SGF and 137 s for SGF-HPMC; and maintained a residual mass of 76% at 800 °C in TGA, compared with 58.3% for SGF and 55.1% for SGF-HPMC. These improvements were associated with the formation of a denser silica-rich protective layer after combustion, which delayed heat transfer to the wood substrate. Under the adopted direct-flame screening conditions, SGF-HPMC-SOL exhibited enhanced flame-retardant performance compared with the reference gel foams, indicating its potential for enhanced flame-retardant performance under laboratory screening conditions for forest fire prevention. [ABSTRACT FROM AUTHOR] |
| Copyright of Materials (1996-1944) is the property of MDPI and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
|
Full text is not displayed to guests.
Login for full access.
|
|
| Abstract: | Highlights: A composite of water glass/HPMC/silica sol (SGF-HPMC-SOL) was constructed. A stable organic–inorganic hybrid network enhances the material's properties. Its flame-retardant performance is superior to that of traditional gels. To meet the requirements of forest fire prevention, a water glass-based composite gel foam was developed by introducing hydroxypropyl methylcellulose (HPMC) and nanosilica sol into a sodium silicate/sodium bicarbonate matrix. The resulting water glass/HPMC/silica sol ternary system (SGF-HPMC-SOL) was designed to improve water retention, foam stability, substrate adhesion, and fire-barrier durability. The results indicate that HPMC and silica sol contributed to network reinforcement through hydrogen bonding, polymer-chain entanglement, nanoscale filling, and possible interfacial condensation. The optimized SGF-HPMC-SOL retained 20.4% of its initial mass after heating at 100 °C for 5 h, compared with 4.65% for SGF and 9.54% for SGF-HPMC; reached a carbonization time of 164 s under direct-flame exposure, versus 100 s for SGF and 137 s for SGF-HPMC; and maintained a residual mass of 76% at 800 °C in TGA, compared with 58.3% for SGF and 55.1% for SGF-HPMC. These improvements were associated with the formation of a denser silica-rich protective layer after combustion, which delayed heat transfer to the wood substrate. Under the adopted direct-flame screening conditions, SGF-HPMC-SOL exhibited enhanced flame-retardant performance compared with the reference gel foams, indicating its potential for enhanced flame-retardant performance under laboratory screening conditions for forest fire prevention. [ABSTRACT FROM AUTHOR] |
|---|---|
| ISSN: | 19961944 |
| DOI: | 10.3390/ma19122434 |