Kinetics of film formation of poly(n-butyl methacrylate) latex in the presence of poly(styrene/alpha-methylstyrene/acrylic acid) by atomic force microscopy
Dy. Lee et al., Kinetics of film formation of poly(n-butyl methacrylate) latex in the presence of poly(styrene/alpha-methylstyrene/acrylic acid) by atomic force microscopy, LANGMUIR, 15(23), 1999, pp. 8252-8258
The kinetics of film formation of emulsifier-free monodisperse poly(n-butyl
methacrylate) (PBMA) latex in the presence of post-added poly(styrene/alph
a-methylstyrene/acrylic acid) (SAA), an example of alkali soluble resin (AS
R), was followed using atomic force microscopy (AFM). The peak-to-valley di
stance (corrugation height) of latex particles in the film was monitored at
different annealing temperatures as a function of annealing duration. The
influence of the concentration of SAA on the rate of interdiffusion of the
latex particles and hence the film morphology was investigated. The AFM res
ults show that the kinetics obey the time/temperature superposition princip
les. The corrugation height of the PBMA particles in films containing SAA w
as found to be higher than those in the pure PBMA films. The AFM results su
ggest very strongly both the formation of a hard surface layer of SAA over
the soft PBMA particle, and the migration of free SAA to the latex film sur
face during annealing. The SAA layer adsorbed on and surrounding each PBMA
particle retards the interdiffusion of the PBMA molecules across the partic
le-particle interface and slows the gradual coalescence of the particles in
film formation resulting in poorer tensile property of these films compare
d to that of the pure PBMA latex. The two-step kinetics of the film forming
process is the direct consequence of both the interdiffusion rate of PBMA
latex particle and the migration of SAA to the surface of latex films.