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1 cluding other surfaces (glass, aluminum, and porcelain).
2 mount of strengthening of feldspathic dental porcelain.
3 r of crack deflections in leucite-reinforced porcelain.
4 Y-TZP system cores were veneered with 1.5 mm porcelain.
5 nslucency level comparable to that of dental porcelain.
6 ative to alumina and for alumina relative to porcelain.
7 nfluences the degree of microcracking in the porcelain.
8 nts within the normal firing range of dental porcelain.
9 nd flexural strength of a leucite-reinforced porcelain.
10 e porcelain and a 1.5-mm-thick layer of body porcelain.
11 to those of the commercial high-translucency porcelains.
12 resin polymerization shrinkage strengthened porcelains.
13 out infiltration and on crowns veneered with porcelains.
14 s veneer layer 1 mm thick (representative of porcelain), adhesively bonded onto a glass-like core sub
15 prepared with a 0.5-mm-thick layer of opaque porcelain and a 1.5-mm-thick layer of body porcelain.
17 n four dental ceramics: "aesthetic" ceramics-porcelain and micaceous glass-ceramic (MGC), and "struct
18 re fired to the maturing temperature of body porcelain and then were subjected to three cooling proce
19 er grinding increases the strength of dental porcelain and to determine whether the effectiveness of
23 mics, glass-infiltrated alumina, feldspathic porcelain, and transformable zirconiaare presented as ca
24 e much more chip-resistant than conventional porcelains, and at least as chip-resistant as non-infilt
26 rillation, and diabetes but a higher rate of porcelain aorta, lower glomerular filtration rate, and h
32 of cracks induced in the surface of the body porcelain by a microhardness indenter were measured imme
33 measurement of the area fraction of retained porcelain by an x-ray spectrometric technique described
34 the thermal expansion of leucite-reinforced porcelain can be lowered by ion-exchange, which also mod
35 ovides evidence that microcracking in dental porcelain can be minimized by a reduction of the mean le
37 nd cement moved the fracture origin from the porcelain/cement interface to the cement surface, consis
39 radically in the two bilayer systems: In the porcelain coatings, cone cracks initiate at the coating
42 are observed in the fine glass-ceramics and porcelain; conversely, the most quasi-plastic responses
43 hether multiple firings of commercial dental porcelains could produce changes in microcrack density.
49 orm of leucite in a leucitereinforced dental porcelain, evaluate its effect on the flexural strength,
51 (r2 = 0.24, p = 0.0003), while the remaining porcelain exhibited a weak but statistically significant
54 compressive stresses in the surface of body porcelain for all of the thermal contraction mismatch ca
55 i2O6) is used as a reinforcing agent in some porcelains for all-ceramic restorations; however, it inc
56 s around them, f(mc), was estimated for each porcelain from the microcrack density and the leucite su
57 rosthetic restoration needed: 1) single unit porcelain-fused-to-metal (PFM) crowns (SCs) and 2) 3- to
59 ich thermal mismatch stresses can develop in porcelain-fused-to-metal restorations, i.e., from room t
60 elains that are designed to be fused to PFM (porcelain-fused-to-metal) alloys are formulated by their
61 the conversion of leucite to sanidine during porcelain heat treatments would produce a detrimental lo
62 r the mean leucite particle size of a dental porcelain influences the degree of microcracking in the
63 ies have shown that, when feldspathic dental porcelain is cooled, leucite undergoes a transformation
66 to both occlusal surface contact damage and porcelain lower surface radial fracture, while porcelain
67 d these leucite particles when cooled during porcelain manufacture are a potential source of change i
69 .947) between the area fractions of retained porcelain measured in the present study and the oxide ad
71 indered the elucidation of the mechanism for porcelain-metal bonding in dental systems, because a tes
72 test capable of detecting differences among porcelain-metal bonds of various qualities is required b
73 ce for the presence of an oxide layer at the porcelain-metal interface, provides compelling support f
74 onversion on porcelain thermal expansion and porcelain-metal thermal compatibility have been uncertai
78 rcelain lower surface radial fracture, while porcelain on a higher-hardness palladium-silver alloy fr
80 posite extremes of elastic/plastic mismatch: porcelain on glass-infiltrated alumina ("soft/hard"); an
83 Controls were made of untreated Optec HSP porcelain powder, formed into bars and disks, and baked
89 results of this study indicate that even for porcelains that exhibit a measurable change in microcrac
91 ure are a potential source of change in bulk porcelain thermal expansion during fabrication of porcel
93 systems included chipping or fracture of the porcelain veneer initiating at the indentation site.
94 be predominantly chips and fractures in the porcelain veneer, from occlusally induced sliding contac
96 ch, clinical long-term studies indicate that porcelain-veneered alumina or zirconia full-coverage cro
101 nia is more than 4 times higher than that of porcelain-veneered zirconia and is at least as high as t
104 To test this hypothesis, we cemented flat porcelain-veneered zirconia plates onto dental composite
105 to veneer chipping and fracture relative to porcelain-veneered zirconia, while providing necessary e
107 ations, whether monolithic (single layer) or porcelain-veneered, often chip and fracture from repeate
112 the current study indicate that re-firing of porcelain with large surface flaws does not significantl
113 ciated with combinations containing the body porcelain with the smaller contraction coefficient.
114 ction of cracked particles compared with the porcelains with mean leucite particle diameters above Dc
117 e trilayer, post mortem damage evaluation of porcelain/zirconia/composite trilayers by a sectioning t
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