Low temperature heat capacities of Ti3Al1.1C1.8, Ti4AlN3, and Ti3SiC2

dc.contributor.author	Ho, J. C.	en_US
dc.contributor.author	Hamdeh, Hussein H.	en_US
dc.contributor.author	Barsoum, M. W.	en_US
dc.contributor.author	El-Raghy, T.	en_US
dc.date.accessioned	2011-12-20T23:52:17Z
dc.date.available	2011-12-20T23:52:17Z
dc.date.issued	1999-10-01	en_US
dc.identifier.citation	Ho, J.C.; Hamdeh, H.H.; Barsoum, M.W.; El-Raghy, T.; , "Low temperature heat capacities of Ti3Al1.1C1.8, Ti4AlN3, and Ti3SiC2," Journal of Applied Physics , vol.86, no.7, pp.3609-3611, Oct 1999.doi: 10.1063/1.371267	en_US
dc.identifier.issn	0021-8979	en_US
dc.identifier.uri	http://dx.doi.org/10.1063/1.371267	en_US
dc.identifier.uri	http://hdl.handle.net/10057/4075
dc.description	The full text of this article is not available on SOAR. WSU users can access the article via IEEE Xplore database licensed by University Libraries: http://libcat.wichita.edu/vwebv/holdingsInfo?bibId=1045955	en_US
dc.description.abstract	For the binary Ti Al system, an ordering transformation in Ti3Al has been shown to result in a significant lowering of the electronic heat-capacity coefficient, ?, by removing electrons from conducting states. When ? is normalized to a per Ti atom basis, the same tendency is found in low temperature calorimetric studies of the conducting ternary carbides Ti3Al1.1C1.8, Ti4AlN3, and Ti3SiC2 reported herein. As a consequence of C- or N-induced covalent-like bond formation, the Debye temperatures in these ternaries are in excess of 700 K. © 1999 American Institute of Physics.	en_US
dc.language.iso	en_US	en_US
dc.publisher	IEEE	en_US
dc.relation.ispartofseries	Journal of Applied Physics , vol.86, no.7, pp.3609-3611.	en_US
dc.subject	Debye temperature	en_US
dc.subject	Aluminium alloys	en_US
dc.subject	Specific heat	en_US
dc.subject	Titanium alloys	en_US
dc.title	Low temperature heat capacities of Ti3Al1.1C1.8, Ti4AlN3, and Ti3SiC2	en_US
dc.type	Article	en_US
dc.description.version	Peer reviewed article	en_US
dc.rights.holder	© IEEE, 1999	en_US