Influence of monofunctional reactants on the physical properties of dimer acid‐based polyamides

Polymers for Advanced Technologies - Tập 17 Số 1 - Trang 30-36 - 2006
Selva Çavuş1, M. Ali Gürkaynak1
1Department of Chemical Engineering, Faculty of Engineering, Istanbul University, 34320 Avcılar, Istanbul, Turkey

Tóm tắt

Abstract

Dimer acid‐based polyamides were synthesized by condensation polymerization in the absence and presence of monofunctional reactants. Acetic acid, oleic acid and propyl amine were used as monofunctional reactants. The influences of the equivalent percentage (E%) and type of monofunctional reactant on the physical properties of dimer acid‐based polyamides such as glass transition temperature (Tg), melting point (Tm), heat of fusion (ΔH), degree of polymerization (DP), number average molecular weight (Mn), and kinematic viscosity were investigated. The molecular weight and viscosity of dimer acid‐based polyamides decreased with the increase in equivalent percentage of monofunctional reactant. Differential scanning calorimetry (DSC) studies showed that acetic acid and propyl amine had higher effect on the thermal properties of polyamides than that of oleic acid. In the case of polyamides prepared in the presence of acetic acid, the values of Tg, Tm, and ΔH of the polyamides increased remarkably with the increase in acetic acid content. On the contrary, propyl amine had a decreasing effect on the values of Tg, Tm, and ΔH of the polyamides. Incorporation of oleic acid into the polymer structure had no significant effect on the values of Tg and Tm of the dimer acid‐based polyamides. Copyright © 2006 John Wiley & Sons, Ltd.

Từ khóa


Tài liệu tham khảo

Peerman DE, 1969, Encyclopedia of Polymer Science and Technology, Vol. 10: Polyamides from Fatty Acids, 597

Leonard EC, 1979, Encyclopedia of Chemical Technology, Vol. 7: Dimer Acids, 768

10.1016/S0143-7496(01)00039-2

Byrne LF, 1962, The chemistry, manufacture, and uses of dimerized fatty acids, Paint Technology, 26, 28

10.1007/BF02672546

Floyd DE, 1966, Polyamide Resins, 33

10.1002/(SICI)1097-4628(19980411)68:2<305::AID-APP12>3.0.CO;2-W

10.1002/(SICI)1097-4628(19991107)74:6<1563::AID-APP31>3.0.CO;2-0

10.1002/(SICI)1097-4628(19990808)73:6<1081::AID-APP27>3.0.CO;2-J

10.1016/0032-3861(92)91109-F

WhyzmuzisPD SpinksAE.Henkel Co. US Patent 4 508 868 April 2 1985.

RumackDT.Union Camp Co. US Patent 4 816 549 March 28 1989.

Van BeekDA.Henkel Co. US Patent 5 138 027 August 11 1992.

10.1021/ja01182a097

Sweeny W, 1969, Encyclopedia of Polymer Science and Technology, Vol. 10: Polyamides, 483

10.1016/S0014-3057(98)00277-8

10.1002/(SICI)1099-0488(199703)35:4<595::AID-POLB7>3.0.CO;2-P

10.1016/S0032-3861(02)00299-9

10.1081/MA-120028207