Abstract

This article reports on the synthesis, thermal behavior, and morphology of phase change materials based on diesters from 1,4-butanediol with palmitic (BD16), stearic (BD18), or behenic (BD22) acid. The crystalline contents and melting enthalpies of all substances exceed 90% and 180 J/g, respectively. The molecules display monotropic polymorphism. The metastable β′ form is built from outstretched molecules, whereas the denser, stable β form is composed of molecules with a kinked conformation. BD18 and BD22 crystallize into the β′ form during cooling. Only BD18 transforms into the β form during subsequent heating via a solid–solid transition. The resistance of BD22 to convert into the β form is believed to originate from the lack of mobility associated with longer aliphatic chains. In contrast, the polymorphic conversion is thought to be very efficient and to take place during cooling for the shorter BD16 molecules. The hypothesis is put forward that the original BD16 β′ nuclei are rapidly overgrown by the ...

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.