In this research, the preparation and characterization of polypropylene (PP) and natural zeolite composites were studied. Natural zeolite mined in Gordes, Turkey was used as an alternative filler to CaCO3. Films were prepared by the extrusion of PP, and surface-modified zeolite was made by polyethylene glycol 4000 with 2–4% zeolite. Zeolite-filled composites had densities between 0.73 and 0.83 g/cm3 and had void fractions of 0.07–0.20. Although the permeability of water vapor through 2% zeolite-filled composites was very small, 4% zeolite-filled films had very high permeabilities. The yield stresses of 2–4% zeolite-containing films were around 26–27 N/mm2 and were lower than that of PP, which indicated no adhesion between PP and zeolite. The effect of zeolite on the thermal degradation behavior in air and in a N2 atmosphere was also studied. In air, zeolites did not cause the oxidation of PP. In a N2 atmosphere, although the start of the thermal degradation of PP was retarded by zeolite, composites degraded at a faster rate than PP once the degradation started. At a processing temperature of 200°C, zeolites had no effect on the degradation of PP. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 2913–2921, 2001
[1]
M. Tosi,et al.
Local Structures in Aluminum Oxide
,
1999
.
[2]
D. Balköse,et al.
Diffusivity, solubility and permeability of water vapor in flexible PVC/silica composite membranes
,
1996
.
[3]
J. Hlavay,et al.
A simple method for the determination of clinoptilolite in natural zeolite rocks
,
1995
.
[4]
L. Domka.
Modification estimate of kaolin, chalk, and precipitated calcium carbonate as plastomer and elastomer fillers
,
1994
.
[5]
Shingo Kaneko,et al.
Microporous polypropylene sheets containing CaCO3 filler
,
1993
.
[6]
T. Kowalewski,et al.
High orientation of toughened chalk-filled isotactic polypropylene : preparation and properties
,
1992
.
[7]
Y. Mizutani,et al.
Structure of microporous polypropylene sheets containing CaCO3 filler
,
1992
.
[8]
A. Horrocks,et al.
Physicochemical changes in stabilized, orientated polypropylene films during the initial stages of thermal oxidation
,
1991
.