Mechanical behavior of cellular borosilicate glass with pressurized Ar-filled closed pores
Source abstract
Abstract
Abstract High strength borosilicate foams were fabricated by melting glass powder under high-pressure argon gas and subsequent heat treatment of the glass bulk at atmospheric pressure. In the first step, borosilicate glass powder was melted at 1100 °C for 1 h by capsule-free hot isostatic pressing (HIPing) under a high gas pressure of 10–70 MPa. Pressurized Ar-filled spherical pores were introduced into the glass, and argon atoms were dissolved in the glass network structure. The expansion of argon-filled pores and the release of the dissolved Ar gas resulted in the formation of pressurized Ar-filled closed pores by isothermal heat treatment at 800 °C for 10 min. A high porosity of up to 80% with a bimodal distribution of micro-size cells was obtained for the resultant cellular borosilicate glass. By increasing the total gas pressure from 10 to 70 MPa, the compressive strength and the Young’s modulus were increased considerably from 15 to 52 MPa and from 4.1 to 12.6 GPa, respectively, which can be substantially attributed to the high collapse stress from the high enclosed gas pressure. The cellular glass with a high porosity showed a large failure strain under uniaxial compression.
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Research context
OpenAlex topics: Polymer Foaming and Composites · Cellular and Composite Structures · Flame retardant materials and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (34)
Show source-provided references
1. Onck · Int J Mech Sci · 2001 · 43 · 68110.1016/S0020-7403(00)00042-4 ↗
2. Kovacik · Scripta Mater · 1998 · 39 · 23910.1016/S1359-6462(98)00151-1 ↗
3. Schwartzwalder K, Somers AV. US patent no 3090094; May 21, 1963.
4. Saggio-Woyansky · Am Ceram Soc Bull · 1992 · 71 · 1674
5. Sepulveda · J Eur Ceram Soc · 1999 · 19 · 205910.1016/S0955-2219(99)00024-2 ↗
6. Peng · J Eur Ceram Soc · 2000 · 20 · 80710.1016/S0955-2219(99)00229-0 ↗
7. Rambo · J Am Ceram Soc · 2006 · 89 · 337310.1111/j.1551-2916.2006.01247.x ↗
8. Fernandes · Ceram Int · 2007 · 33 · 96310.1016/j.ceramint.2006.02.010 ↗
9. Guo · Mater Lett · 2010 · 64 · 99710.1016/j.matlet.2010.02.006 ↗
10. Tulyaganov · J Porous Mater · 2006 · 13 · 13310.1007/s10934-006-7014-9 ↗
11. Kearns · Adv Eng Mater · 1987 · 3 · 85
12. Murray · Acta Mater · 2004 · 52 · 226910.1016/j.actamat.2004.01.039 ↗
13. Murray · Acta Mater · 2004 · 52 · 227910.1016/j.actamat.2004.01.019 ↗
14. Wu · Acta Mater · 2007 · 55 · 343710.1016/j.actamat.2007.01.045 ↗
15. Baldwin · Polym Eng Sci · 1996 · 36 · 143710.1002/pen.10538 ↗
16. Gibson · 1999
17. Pye · 2005
18. Davis · J Mater Res · 2001 · 16 · 150810.1557/JMR.2001.0210 ↗
19. Murray · Scripta Mater · 2003 · 49 · 87910.1016/S1359-6462(03)00438-X ↗
20. Murray · Compos Sci Technol · 2003 · 63 · 231110.1016/S0266-3538(03)00264-1 ↗
21. Bernacrdo · Ceram Int · 2007 · 33 · 96310.1016/j.ceramint.2006.02.010 ↗
22. Bernardo · Ceram Int · 2006 · 32 · 60310.1016/j.ceramint.2005.04.019 ↗
23. Hattiangadi · J Am Ceram Soc · 2000 · 83 · 273010.1111/j.1151-2916.2000.tb01624.x ↗
24. Rice · J Mater Sci · 1997 · 32 · 473110.1023/A:1018674713006 ↗
25. Yang · Acta Mater · 2002 · 50 · 483110.1016/S1359-6454(02)00350-6 ↗
26. Pabst · J Mater Sci Lett · 2003 · 22 · 95910.1023/A:1024600627210 ↗
27. Pabst · J Mater Sci · 2003 · 39 · 350110.1023/B:JMSC.0000026961.12735.2a ↗
28. Pabst · J Mater Sci · 2003 · 39 · 321310.1023/B:JMSC.0000025863.55408.c9 ↗
29. Pabst · AIP Conf Proc · 2009 · 1145 · 10910.1063/1.3179837 ↗
30. Kovacik · J Mater Sci · 2001 · 20 · 1953
31. Liu · Acta Mater · 2003 · 51 · 36510.1016/S1359-6454(02)00400-7 ↗
32. Prberts · Acta Mater · 2001 · 49 · 18910.1016/S1359-6454(00)00314-1 ↗
33. Prberts · J Mech Phys Solids · 2002 · 50 · 3310.1016/S0022-5096(01)00056-4 ↗
34. Spriggs · J Am Ceram Soc · 1961 · 44 · 62810.1111/j.1151-2916.1961.tb11671.x ↗