Properties
of Discus Dental Composites

Investigation:
John M. Powers, Ph.D.
Director, Houston Biomaterials Research Center
University of Texas-Houston Health Science Center, Dental Branch
6516 John Freeman, Houston, TX 77030-3402
Telephone (713) 500-4470; Fax (713) 500-4500
Date Posted: April 6, 2000
Color and color stability after
accelerated aging
Specimens (2 mm in thickness and 10 mm in
diameter) were prepared in split stainless steel rings. After baseline
measurements of color were made as described below, the specimens
were aged artificially in a weathering machine (Atlas Ci35 Weather-Ometer)
with exposure to a controlled-irradiance xenon arc filtered through
borate borosilicate glass at 0.55 W/m2/nm @ 340 nm, a black panel
temperature of 70 °C (light) and 38 °C (dark), dry bulb temperature
of 47 °C (light) and 38 °C (dark), and humidity of 50% (light) and
95% (dark). The test cycle was 40 min light only, 20 min light plus
front water spray, 60 min light only, and 60 min dark plus back
water spray. Specimens were evaluated for changes for an energy
exposure of 150 kJ/m2 @ 340 nm. CIE L*a*b* relative to CIE standard
illuminant C was measured against white backgrounds on a reflection
spectrophotometer (Macbeth 7000) at baseline and after each aging
interval. Delta E* was calculated.
Polymerization shrinkage
Density of specimens before and after polymerization
was calculated by a water displacement technique using a 2-mL pyncometer.
The change in density was the volumetric shrinkage. Linear shrinkage
was calculated by dividing volumetric shrinkage by three.
Depth
of cure
Specimens were made in molds in thickness
varying from 0.5 to 6.0 mm in increments of 0.5 mm. Barcol hardness
measurements were made of the top and bottom surfaces of the specimen
after light curing the specimens. Depth of cure was defined as the
maximum thickness of the specimen where the top and bottom hardness
measurements did not differ by more than 10%.
Water
sorption