Quanxiao Dong
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Quanxiao Dong has a total of 36 co-authors. Here are the top co-authors by number of shared publications:
Erpo Wang
Beijing Building Construction Research Institute, Co., Ltd
2 shared publicationsFeng Wang
Chinese Academy of Sciences
2 shared publicationsKui He
Zhejiang University
2 shared publications- Mingshu Yang
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Engineering Plastic Institute of Chemistry, Chinese Academy of Sciences Beijing China
2 shared publications Chong Gao
University of Chinese Academy of Sciences
1 shared publicationFangfang Jia
Beijing Building Construction Research Institute, Co., Ltd
1 shared publication
Latest Publications
- Open Access
- 21 June 2021
- Published by Frontiers Media SA in Frontiers in Materials
- Vol. 8
Improvement of Flame Retardancy of Polyurethane Foam Using DOPO-Immobilized Silica Aerogel
In this work, silica aerogel was modified by 9,10-dihydro-9-oxa-10-phosphaphenanthrene-1-oxide (DOPO). Then DOPO-immobilized silica aerogel nanoparticles were used as a flame retardant to prepare flame-retardant polyurethane foams. Microscale combustion calorimeter and cone calorimeter tests were employed to evaluate the flame retardancy of polyurethane foams. It was found that both the heat release rate and the total heat release of the composites were reduced with the incorporation of DOPO immobilized silica aerogel. It is speculated that the DOPO-immobilized silica aerogel nanoparticles can inhibit the degradation of polyurethane and catalyze the formation of carbonaceous carbon on the surface.
- 21 June 2021
- Published by Frontiers Media SA in Frontiers in Materials
- Vol. 8
Open AccessImprovement of Flame Retardancy of Polyurethane Foam Using DOPO-Immobilized Silica Aerogel
In this work, silica aerogel was modified by 9,10-dihydro-9-oxa-10-phosphaphenanthrene-1-oxide (DOPO). Then DOPO-immobilized silica aerogel nanoparticles were used as a flame retardant to prepare flame-retardant polyurethane foams. Microscale combustion calorimeter and cone calorimeter tests were employed to evaluate the flame retardancy of polyurethane foams. It was found that both the heat release rate and the total heat release of the composites were reduced with the incorporation of DOPO immobilized silica aerogel. It is speculated that the DOPO-immobilized silica aerogel nanoparticles can inhibit the degradation of polyurethane and catalyze the formation of carbonaceous carbon on the surface.
- Open Access
Investigation of Flame Retardant Flexible Polyurethane Foams Containing DOPO Immobilized Titanium Dioxide Nanoparticles
In this work, a multi-functional nanoparticle (TiO2-KH570-DOPO) has been successfully synthesized through the attachment of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO)-methacryloxy propyl trimethoxyl silane on the surface of titanium dioxide (TiO2). Supercritical carbon dioxide was used as the solvent in order to increase the grafting level. The chemical structure of TiO2-KH570-DOPO was fully characterized using Fourier transform infrared spectra, thermogravimetric analysis and transmission electron microscopy. The modified TiO2 was incorporated into flexible polyurethane foam (FPUF). The fire performance of FPUF blends was evaluated using microscale combustion calorimetry. Peak heat release rate and total heat release values were reduced from 657.0 W/g and 28.9 kJ/g for neat FPUF sample to 519.2 W/g and 26.8 kJ/g of FPUF specimen containing 10 wt % of TiO2-KH570-DOPO. Analysis of thermal stability and the observation of char formation suggests that TiO2-KH570-DOPO is active in the condensed phase.
Open AccessInvestigation of Flame Retardant Flexible Polyurethane Foams Containing DOPO Immobilized Titanium Dioxide Nanoparticles
In this work, a multi-functional nanoparticle (TiO2-KH570-DOPO) has been successfully synthesized through the attachment of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO)-methacryloxy propyl trimethoxyl silane on the surface of titanium dioxide (TiO2). Supercritical carbon dioxide was used as the solvent in order to increase the grafting level. The chemical structure of TiO2-KH570-DOPO was fully characterized using Fourier transform infrared spectra, thermogravimetric analysis and transmission electron microscopy. The modified TiO2 was incorporated into flexible polyurethane foam (FPUF). The fire performance of FPUF blends was evaluated using microscale combustion calorimetry. Peak heat release rate and total heat release values were reduced from 657.0 W/g and 28.9 kJ/g for neat FPUF sample to 519.2 W/g and 26.8 kJ/g of FPUF specimen containing 10 wt % of TiO2-KH570-DOPO. Analysis of thermal stability and the observation of char formation suggests that TiO2-KH570-DOPO is active in the condensed phase.
- 23 August 2016
- Published by Springer Nature in Science China Chemistry
- Vol. 59 (10) , 1283-1290
Isothermal crystallization of polypropylene/surface modified silica nanocomposites
- 23 August 2016
- Published by Springer Nature in Science China Chemistry
- Vol. 59 (10) , 1283-1290
Isothermal crystallization of polypropylene/surface modified silica nanocomposites
- 5 June 2014
- Published by Springer Nature in Journal of Wuhan University of Technology-Mater. Sci. Ed.
- Vol. 29 (3) , 498-503
Effect of matrix modification on durability of cementitious composites in an acid rain environment
- 5 June 2014
- Published by Springer Nature in Journal of Wuhan University of Technology-Mater. Sci. Ed.
- Vol. 29 (3) , 498-503
Effect of matrix modification on durability of cementitious composites in an acid rain environment
- 21 September 2013
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 131 (4)
Synergistic effect of aluminum hydroxide and expandable graphite on the flame retardancy of polyisocyanurate–polyurethane foams
For the first time, expandable graphite (EG) and aluminum hydroxide (ATH) was combined to improve the flame retardancy of polyisocyanurate–polyurethane (PIR–PUR) foam. The limited oxygen index increased from 26.5 for the PIR–PUR matrix to an incredible value of 92.8 when 24 phr (parts per 100 of matrix) EG and 60 phr ATH were incorporated into the matrix. Based on morphology observation and thermogravimetric analysis, it was speculated that two factors contributed to the improvement of flame retardancy primarily. First, ATH could effectively induce “villi” like particles, which was useful to form a dense char. The compact char layer could effectively impede the transport of bubbles and heat. Second, ATH and EG accelerated the initial degradation and fluffy char was quickly generated on the surface of the composites. Thus, the degradation of the composite was slowed down and the diffusion of volatile combustible fragments to flame zone was delayed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 39936.
- 21 September 2013
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 131 (4)
Synergistic effect of aluminum hydroxide and expandable graphite on the flame retardancy of polyisocyanurate–polyurethane foams
For the first time, expandable graphite (EG) and aluminum hydroxide (ATH) was combined to improve the flame retardancy of polyisocyanurate–polyurethane (PIR–PUR) foam. The limited oxygen index increased from 26.5 for the PIR–PUR matrix to an incredible value of 92.8 when 24 phr (parts per 100 of matrix) EG and 60 phr ATH were incorporated into the matrix. Based on morphology observation and thermogravimetric analysis, it was speculated that two factors contributed to the improvement of flame retardancy primarily. First, ATH could effectively induce “villi” like particles, which was useful to form a dense char. The compact char layer could effectively impede the transport of bubbles and heat. Second, ATH and EG accelerated the initial degradation and fluffy char was quickly generated on the surface of the composites. Thus, the degradation of the composite was slowed down and the diffusion of volatile combustible fragments to flame zone was delayed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 39936.