[vc_empty_space][vc_empty_space]
Structure and properties of polymers prepared by polymerization of 2,2-dimethyl-1,3-propandiol and ε-caprolactone monomer
Arcana M.I.a, Hasan M.a, Anggraini S.D.a, Febrianti A.A.a, Ardana A.a
a Inorganic and Physical Chemistry Research Division, Faculty of Mathematic and Natural Sciences, Institut Teknologi Bandung, Indonesia
[vc_row][vc_column][vc_row_inner][vc_column_inner][vc_separator css=”.vc_custom_1624529070653{padding-top: 30px !important;padding-bottom: 30px !important;}”][/vc_column_inner][/vc_row_inner][vc_row_inner layout=”boxed”][vc_column_inner width=”3/4″ css=”.vc_custom_1624695412187{border-right-width: 1px !important;border-right-color: #dddddd !important;border-right-style: solid !important;border-radius: 1px !important;}”][vc_empty_space][megatron_heading title=”Abstract” size=”size-sm” text_align=”text-left”][vc_column_text]Poly(ε-caprolactone) (PCL) is very attractive synthetic polymer due to its properties, such as a high permeability, the lack of toxicity, and also biodegradability. However, it has limited application because of low melting point (60 oC), high crystallinity, and brittleness. The aim of the experiments is designed to improve the properties of PCL by formation of their polymers with 2,2-dimethyl-1,3-propandiol monomers with various chain length as a raw material to prepare poly(urethane-ester). These polymers were synthesized by a ring-opening polymerization of 2,2-dimethyl-1,3-propandiol and ε-caprolactone monomers in various composition in the presence of 1-hydroxy-3-chloro-tetraisobuthyldistanoxane as a catalyst. Polymers were characterized by analysis of functional groups (FTIR), microstructure (1H and 13C NMR), viscosity, hydroxyl number, and also melting point of polymers (DSC). Based on the structure analysis indicate that polymerization of 2,2-dimethyl-1,3-propandiol and ε-caprolactone monomers produced polymers with various molecular weights, which depend on the ratio of ε-caprolactone/2,2-dimethyl-1,3-propandiol used in polymerization. The reactivity of CL monomer decreases to the active site of polymers with longer chain size. The melting points of polymers increase with the increasing of ε-caprolactone composition used in polymerization, whereas hydroxyl number decreases.[/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Author keywords” size=”size-sm” text_align=”text-left”][vc_column_text][/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Indexed keywords” size=”size-sm” text_align=”text-left”][vc_column_text]Block polymer,Caprolactone,Distannoxane,Propandiol,Properties[/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Funding details” size=”size-sm” text_align=”text-left”][vc_column_text][/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”DOI” size=”size-sm” text_align=”text-left”][vc_column_text]https://doi.org/10.5614/itbj.sci.2009.41.2.2[/vc_column_text][/vc_column_inner][vc_column_inner width=”1/4″][vc_column_text]Widget Plumx[/vc_column_text][/vc_column_inner][/vc_row_inner][/vc_column][/vc_row][vc_row][vc_column][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][/vc_column][/vc_row]