Self stress generated in polymer impregnated gypsum (referred as GPC)
when it is composed is estimated, and its influence on flexural streng
th is discussed. The estimation of the self stress is based on measure
d values of shrinkage caused by polymerization of impregnated monomer
and elastic modulus of dried gypsum base just before impregnation. The
effect of this self stress on flexural strength of GPC is investigate
d. It was found that the following equation is valid to predict flexur
al strength of GPC (6(b)) in terms of the self stress as a variable: 6
(b) = 6(gb) + V-p (6(p) - 6(sp)), where 6(gb) = flexural strength of g
ypsum base, V-p = specific volume of polymer, 6(p) = tensile strength
of polymer, and 6(sp) = self stress generated in polymer phase. If ext
remely low water-gypsum ratio is adopted to prepare gypsum base, crack
ing is observed just after polymerization preceding any flexural loadi
ng. For somewhat higher water-gypsum ratio, specimens are not cracked,
but their flexural strength is decreased after polymer impregnation.
The self stress corresponding to this case turns out to be higher than
the tensile strength of polymethyl methacryrate used for the impregna
tion. Since prediction of 6(sp) in the equation is based on tri-axial
compressive strain of gypsum base that is within its elastic region, 6
(sp) in polymer phase should positively exist. Even for this condition
, the validity of the equation seems to be maintained, although the va
lue in the parenthesis of the equation becomes negative. Based on this
fact, an unstable physical state where one phase of a composite mater
ial is stressed beyond its macroscopic strength as an individual mater
ial owing to the crack arresting effect of the other phase (gypsum in
this case) has been postulated. This state is designated as a ''super-
stressed'' state, taking its resemblance with supercooling or super-sa
turated into consideration. (C) 1998 Elsevier Science Ltd.