期刊文献+

基于原位反应法制备新型复合防火玻璃技术的研究 被引量:2

Preparation of the New Multi-laminated Fire-resistant Glass Based on the In-situ Reaction
下载PDF
导出
摘要 通过对亲水性纳米SiO2颗粒的筛选、调整分散液体系的pH值,制备出具有剪切变稀的特性、固含量为40%、黏度仅为(1 100±18.5)mPa·s的纳米SiO2微粒分散液,再凭借"原位反应法"的特殊工艺制备出无机复合防火玻璃,可具备曲面结构(如弧面幕墙玻璃)。研究结果表明:这种新型的复合防火玻璃具有透过率高、耐温性能好、耐候性优异的特点,其耐紫外线辐照性能超过1 000 h;按照GB 15763.1—2009《建筑用安全玻璃第1部分:防火玻璃》和GB/T 12513—2006《镶玻璃构件耐火试验方法》所规定的方法,在国家建筑工程质量监督检验中心通过90 min耐火完整性测试,满足A1.50h级防火玻璃的技术要求。 By screening the hydrophilic nano SiO2 particles and adjusting the pH value of the system,the dispersion of nano SiO2 particles with a shear thinning characteristic,a solid content of 40%,and a viscosity of(1100±18.5)mPa·s was prepared.The multi-laminated fire-resistant glass with curved surface by the special process of the in-situ reaction method had been applied to the cambered curtain wall glass.The results show that this glass has the advantages of high transmittance,good temperature resistance,and excellent weather resistance characteristics.The anti-ultraviolet irradiation performance of refractory glass is more than 1000 h.According to GB 15763.1—2009 and GB/T 12513—2006,the multi-laminated fire-resistant glass has passed the 90 minutes fire integrity tests by the national center for quality supervision and test of building engineering which meet the technical requirements of A1.50 h grade.
作者 杨幼然 杨磊 穆元春 YANG Youran;YANG Lei;MU Yuanchun(China Building Materials Academy,Beijing 100024,China;State Key Laboratory ofGreen Building Materials,Beijing 100024,China)
出处 《玻璃》 2020年第9期1-7,共7页 Glass
基金 国家重点研发计划项目,复合防火玻璃制造技术与产业化示范(2016YFB0303904)。
关键词 SiO2分散液 黏度 剪切速率 原位反应法 复合防火玻璃 SiO2 dispersion viscosity shear rate in-situ reaction multi-laminated fire-resistant glass
  • 相关文献

参考文献3

二级参考文献31

  • 1Li Z. , Li X. W. , Zheng L. Q. , Lin X. H. , Geng F. , Yu L.. Chem. Res. Chinese Universities[J] , 2010, 26(1) : 136-141.
  • 2Colombini D., Ljungberg N., Hassander H., Karlsson O. J.. Polymer[J], 2005, 46(4): 1295-1308.
  • 3Adler H. J. , Karsten J. , Bettina V. B.. Prog. Org. Coat. [J], 2001,43(4) : 251-257.
  • 4Stefan S. , Katharina L. , Gunter L. , Christine B. , Hans W. S. , Norbert E.. Macromol. Chem. Phys. [J], 1995, 196(4) : 985-993.
  • 5Jonsson J. E. L. , Hassander H. , Jansson L. H. , Tornell B.. Macromolecules[J], 1991,24(1) : 126-131.
  • 6Kirsch S. , Doerk A. , Bartsch E. , Sillescu H. , Landfester K. , Spiess H. W. , Maechtle W.. Macromolecules [ J ], 1999, 32 (14) : 4508-4518.
  • 7Gonzalez-Ortiz L. J. , Asua J. M.. Maeromolecules[ J] , 1996, 29(13) : 4520-4527.
  • 8Thickett S. C. , Gilber R. G.. Polymer[J], 2007, 48(24) : 6965-6991.
  • 9Foster A. B. , Lovell P. A. , Rabjohns M. A.. Polymer[J], 2009, 50(7) : 1654-1670.
  • 10Esser R. J., Devona J. E., Setzke D. E., Wagemans L.. Prog. Org. Coat. [J], 1999, 36(1/2):45-52.

共引文献15

同被引文献10

引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部