198 High-performance organic coatings
74. Ramesh S, Tharanikkarasu K, Mahesh G N, Radhakrishnan G (1998),
‘Synthesis, physicochemical characterization, and applications of polyurethane
ionomers: A review’, J Macromol Sci: Rev Macromol Chem Phys, 38(3), 481–
509.
75. Dochniak M J (1994), ‘Anionic water dispersed polyurethane polymer for
improved coatings and adhesives’, US patent 5,354,807.
76. Kim B K, Lee Y M (1994), ‘Aqueous dispersion of polyurethanes containing
ionic and nonionic hydrophilic segments’, J Appl Polym Sci, 54(12), 1809–
1815.
77. Chen Y, Chen Y L (1992), ‘Aqueous dispersions of polyurethane anionomers:
Effects of countercation’, J Appl Polym Sci, 46(3), 435–443.
78. Nachtkamp K, Pedain J, Grammel J (1981), ‘Process for the preparation of
aqueous polyurethane dispersions and solutions’, US patent 4,269,748.
79. Lewandowski K, Krepski L R, Mickus D E, Roberts R R, Heilmann S M,
Larson W K, Purgett M D, Koecher S D, Johnson S A, Mcgurran D J, Rueb
C J, Pathre S V, Thakur K A M (2002), ‘Synthesis and properties of water-
borne self-crosslinkable sulfo-urethane silanol dispersions’, J Polym Sci: Part
A: Polym Chem, 40(17), 3037–3045.
80. Tirpak R E, Markusch P H (1986), ‘Aqueous dispersions of crosslinked poly-
urethanes’, J Coatings Technol, 58(738), 49–54.
81. Narayan R, Chattopadhyay D K, Sreedhar B, Raju K V S N, Mallikarjuna N
N, Aminabhavi T M (2006), ‘Synthesis and characterization of crosslinked
polyurethane dispersions based on hydroxylated polyesters’, J Appl Polym Sci,
99(1), 368–380.
82. Kim H D, Kim T W (1998), ‘Preparation and properties of UV-curable poly-
urethane acrylate ionomers’, J Appl Polym Sci, 67(13), 2153–2162.
83. Hourston D J, Williams G D, Satguru R, Padget J C, Pears D (1999), ‘The
on water-dispersible polyurethanes’, J Appl Polym Sci, 74(3), 556–566.
84. Yang J E, Kong J S, Park S W, Lee D J, Kim H D (2002), Preparation and
the degree of neutralization and counterion’, J Appl Polym Sci, 86(9), 2375–
2383.
85. Visser S A, Cooper S L (1992), ‘Morphology and properties of mixed anion
ionomers’, Polymer, 33(18), 3790–3796.
86. Chen Y, Chen Y L (1992), ‘Aqueous dispersions of polyurethane anionomers:
Effects of countercation’, J Appl Polym Sci, 46(3), 435–443.
87. Argyropoulos J N, Bone C C, Glancy C W (1994), ‘Polyesters particularly
suitable for use in coating compositions which are sprayed with compressed
88. Kim D S, Seo W H (2004), ‘Ultraviolet-curing behavior and mechanical prop-
erties of a polyester acrylate resin’, J Appl Polym Sci, 92(6), 3921–3928.
89. Decker C, Nguyen T, Viet T, Decker D, Weber-Koehl E (2001), ‘UV-radiation
curing of acrylate/epoxide systems’, Polymer, 42(13), 5531–5541.
90. Decker C, Elzaouk B (1995), ‘Laser curing of photopolymers’, in: Current
Trends in Polymer Photochemistry, Allen N S, Edge M, Bellobono I R, Selli
E (editors), Ellis Horwood, New York, p. 130.
91. Mehnert R, Pincus A, Janorsky I, Stowe R, Berejka A (1998), ‘Radiation
curing: definition and basic characteristics’, Chapter I, in: UV & EB Curing
influence of the degree of neutralization, the ionic moiety, and the counterion
properties of waterborne polyurethane–urea anionomers. I. The
influence of
fluids as vicosity reducing agents’, US patent 5,362,519.
© 2008, Woodhead Publishing Limited