TY - JOUR
T1 - Thermal Energy Storage Using Poly(ethylene glycol) Incorporated Hyperbranched Polyurethane as Solid-Solid Phase Change Material
AU - Sundararajan, Swati
AU - Samui, Asit B.
AU - Kulkarni, Prashant S.
N1 - Funding Information:
S.S. greatly appreciates the fellowship provided by Defence Institute of Advanced Technology (DIAT), Pune. This work was supported by the Defence Research and Development Organization (DRDO) via project grant (ERIP/ER/1003883/ M/01/908/2012/D, R&D/1416, dated 28/3/2012), New Delhi, India.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/12/13
Y1 - 2017/12/13
N2 - For efficient energy storage, hyperbranched (HB) architecture was adopted to prepare a series of HB polyurethanes via A2 + B3 approach with isocyanate terminated poly(ethylene glycol) (PEG) as branching unit and phloroglucinol (PG) as aromatic core. The chemical structure of the HB polymer was confirmed using FTIR and NMR. The gel permeation chromatography and solution viscosities indicate polymers of moderately high molecular weights. The thermal behavior and crystalline properties were investigated using differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction, and polarized optical microscopy. A high fusion enthalpy of 146.6 J g-1 at transition temperature of 56 °C was achieved. Thermal stability was found to be quite high (up to 300 °C), and thermal reliability was retained with no chemical degradation after thermal cycling. The polymer exhibited crystalline to amorphous phase change above the transition temperatures and back, which makes it attractive as a polymeric phase change material for thermal energy storage applications.
AB - For efficient energy storage, hyperbranched (HB) architecture was adopted to prepare a series of HB polyurethanes via A2 + B3 approach with isocyanate terminated poly(ethylene glycol) (PEG) as branching unit and phloroglucinol (PG) as aromatic core. The chemical structure of the HB polymer was confirmed using FTIR and NMR. The gel permeation chromatography and solution viscosities indicate polymers of moderately high molecular weights. The thermal behavior and crystalline properties were investigated using differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction, and polarized optical microscopy. A high fusion enthalpy of 146.6 J g-1 at transition temperature of 56 °C was achieved. Thermal stability was found to be quite high (up to 300 °C), and thermal reliability was retained with no chemical degradation after thermal cycling. The polymer exhibited crystalline to amorphous phase change above the transition temperatures and back, which makes it attractive as a polymeric phase change material for thermal energy storage applications.
UR - http://www.scopus.com/inward/record.url?scp=85038426712&partnerID=8YFLogxK
U2 - 10.1021/acs.iecr.7b03330
DO - 10.1021/acs.iecr.7b03330
M3 - Article
AN - SCOPUS:85038426712
SN - 0888-5885
VL - 56
SP - 14401
EP - 14409
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 49
ER -