ライフサイエンスコーパス: zirconia

1 catalyst nanoparticles attached to CNTs are zirconia.

2 n veneered alumina layers, was not found for zirconia.

3 o PBD which was predeposited in the pores of zirconia.

4 te analog of EDTA, as a surface modifier for zirconia.

5 ade by coating polybutadiene (PBD) on porous zirconia.

6 cross-linking PBD on microparticulate porous zirconia.

7 g affinity but not its bonding efficacy with zirconia.

8 d higher retentivity compared to carbon-clad zirconia.

9 is at least as high as that of non-veneered zirconia.

10 t least as chip-resistant as non-infiltrated zirconia.

11 itude longer than that of porcelain-veneered zirconia.

12 tter cementation properties than homogeneous zirconia.

13 esistance comparable with that of monolithic zirconia.

14 luding the most translucent cubic-containing zirconias.

15 and its use as a substitute for carbon-clad zirconia.1,2 In that method, we showed that very close t

16 e observe two distinct growth modalities for zirconia: (1) turbostratic CNTs 2-3 times smaller in dia

17 dration structure of yttria-stabilized cubic zirconia (110) surface in contact with water was determi

18 , or group B using an individualized CAD/CAM zirconia abutment (CARES abutment; Institut Straumann AG

19 etained single crown made of a prefabricated zirconia abutment with pressed ceramic as the veneering

20 veneered with pressed ceramics or on CAD/CAM zirconia abutments veneered with hand buildup technique.

21 t crowns (ICs) based either on prefabricated zirconia abutments veneered with pressed ceramics or on

22 single-cycle sliding damage than monolithic zirconia and 25 times better than veneered zirconia, and

23 used by Lewis acid/base interactions between zirconia and analytes is greatly suppressed.

24 times higher than that of porcelain-veneered zirconia and is at least as high as that of non-veneered

25 Plates of porcelain-veneered zirconia and monolithic zirconia served as controls.

26 ent study is to compare biofilm formation on zirconia and titanium implant surfaces using an in vitro

27 Titania, zirconia, and alumina samples with periodic three-dimens

28 c zirconia and 25 times better than veneered zirconia, and had a fatigue sliding damage resistance co

29 oward various anionic analytes than do other zirconia- and nonzirconia-based ion exchangers.

30 e these problems, many new types of silica-, zirconia-, and polymer-based columns, which provide uniq

31 The existing Ni-yttria-stabilized zirconia anodes in solid oxide fuel cells (SOFCs) perfor

32 ties (e.g., polybutadiene- and carbon-coated zirconia) are serially coupled and independently tempera

33 uctures that resemble specific sites in bulk zirconia, are promising candidates for potential incorpo

34 d high-strength ceramics-namely, alumina and zirconia-are widely accepted as reliable alternatives to

35 ility of phosphate-modified microparticulate zirconia as a support for protein separations.

36 ces between polybutadiene- and carbon-coated zirconia as well as the extraordinary thermal stability

37 sed for uniform decoration of nanostructured zirconia (average particle size 13 nm) on reduced graphe

38 Failures of zirconia-based all-ceramic restorations appear to be pre

39 ry different from those on either silica- or zirconia-based aromatic and aliphatic phases.

40 Unlike metal nanoparticle catalysts, zirconia-based growth should proceed via surface-bound k

41 Using this new zirconia-based phase, a purification protocol is develop

42 ll as the extraordinary thermal stability of zirconia-based phases (thermally stable to 200 degrees C

43 New zirconia-based polymeric cation-exchange HPLC stationary

44 example of protein separations using porous zirconia-based polymeric phases under normal chromatogra

45 Zirconia-based restorations are widely used in prostheti

46 Zirconia-based restorations often fracture from chipping

47 n inclination angle as a simplified model of zirconia-based restorations under occlusion.

48 The T3C combination of silica- and zirconia-based RPLC columns is demonstrated to be a powe

49 synthesized a novel aromatic polymer-coated zirconia-based RPLC stationary phase by chemical adsorpt

50 These new zirconia-based self-assembled nanodielectric (Zr-SAND) f

51 conditions, which will definitely help make zirconia-based supports more useful for bio-separation.

52 The synthesis and use of a zirconia-based, alkali-stable strong anion-exchange stat

53 an octadecylsilane (ODS) and a carbon-coated zirconia (C-ZrO2) column; and tune the selectivity by in

54 aminosilanes for high-flux yttria-stabilized zirconia capillary membranes is presented (macroporous,

55 anotube nucleation and growth shows that the zirconia catalyst neither reduces to a metal nor forms a

56 2 /ZrS (Cp*=Me5 C5 , Bz=benzyl, ZrS=sulfated zirconia) catalyzes the single-face/all-cis hydrogenatio

57 ific challenges associated with full-contour zirconia ceramics, and a brief synopsis on new machinabl

58 itations of the current generation of nickel zirconia cermet SOFC anodes.

59 materials to date--Ni-YSZ (yttria-stabilized zirconia) cermets--suffer some disadvantages related to

60 ylstyrene and diethoxymethylvinylsilane onto zirconia (CMS/VMS-ZrO2).

61 mobilization of bilirubin oxidase (BOx) onto zirconia coated silica nanoparticles (SiO2@ZrONPs)/chito

62 e explore the use of microparticulate porous zirconia coated with cellulose tris(3,5-dimethylphenyl-c

63 -up using primary secondary amine along with zirconia-coated silica particles for extract purificatio

64 d by dispersive solid phase extraction using zirconia-coated silica particles for extract purificatio

65 urthermore, endotoxin adsorbed to the porous zirconia column may be easily removed (depyrogenated) us

66 CDMPC-coated zirconia columns exhibit high stability under normal-pha

67 gnificant reduction in human biofilm mass on zirconia compared with titanium.

68 , post mortem damage evaluation of porcelain/zirconia/composite trilayers by a sectioning technique r

69 Higher zirconia concentrations possess a mesh-like interconnect

70 degree of coiling is dependant on the local zirconia content.

71 rapid-prototyped as a die for fabrication of zirconia core porcelain-veneered crowns.

72 Zirconia cores were much less susceptible to fracture th

73 f glass veneers epoxy-joined onto alumina or zirconia cores, all bonded to a dentin-like polymer base

74 observed for specimens containing alumina or zirconia cores.

75 t and anatomically correct glass-infiltrated zirconia crown materials, and critical loads were measur

76 common failure modes for porcelain-veneered zirconia dental restorations.

77 tly higher than that of the cubic-containing zirconia (e.g., Zpex Smile) and lithia-based glass-ceram

78 nalities and loose beads such as titania and zirconia for phosphopeptide enrichment can be combined.

79 Because of the strong affinity of zirconia for the phosphoric group, nitroaromatic OPs str

80 Low zirconia fractions yield flaky microstructures where zir

81 Clinical relevance for surface treatments of zirconia frameworks in terms of hydrothermal and structu

82 indicate that porcelain-veneered alumina or zirconia full-coverage crowns and fixed dental prosthese

83 These zirconia-glass materials can be engineered in shades fro

84 Graded zirconia-glass structures exhibited over 3 times better

85 We hypothesized that the graded glass/zirconia/glass with external esthetic glass (e-GZG) can

86 Zirconium dioxide (zirconia) has a great affinity for inorganic and organic

87 Zirconia implant surfaces showed a statistically signifi

88 lucency lithium disilicate glass-ceramic and zirconias, including the most translucent cubic-containi

89 ling by veneer-chipping without exposing the zirconia interface.

90 Tungstated zirconia is a robust solid acid catalyst for light alkan

91 ed that the resistance to chipping in graded zirconia is more than 4 times higher than that of porcel

92 Gold (Au) on ceria-zirconia is one of the most active catalysts for the low

93 Yttria-stabilized zirconia is perhaps the material with the most potential

94 Nanofibers borne from zirconia lack an observable graphitic cage consistently

95 he surface of La1-xSrxMnO3/yttria-stabilized zirconia (LSM/YSZ) cathode backbone using Atomic Layer D

96 , we report that nanoscale yttria-stabilized zirconia membranes with lateral dimensions on the scale

97 or deposition of organic compounds on porous zirconia microparticles.

98 It has been hypothesized that zirconia might have a reduced bacterial adhesion compare

99 es and nanofibers (CNTs and CNFs) grown from zirconia nanoparticle catalysts versus typical oxide-sup

100 oxide (ZrO2-RGO) to avoid coagulation of the zirconia nanoparticles and to obtain enhanced electroche

101 fractions yield flaky microstructures where zirconia nanoparticles arrest propagating cracks.

102 Zirconia nanoparticles embedded in these carbon aerogels

103 Zirconia nanoparticles were electrodynamically deposited

104 we further demonstrate that preannealing of zirconia nanoparticles with a solid-state amorphous carb

105 growth of fibrous carbon nanostructures from zirconia nanoparticles.

106 all nickel oxide clusters supported on ceria-zirconia (NiO/CZ) can convert methane to methanol and et

107 the NU-1000 framework structure, drawing the zirconia nodes closer together, and also underlies the s

108 n the smallest pores of NU-1000, between the zirconia nodes, serving to connect these nodes along the

109 al has been compared to polybutadiene-coated zirconia, octadecyl- and phenyl-bonded silica, and polym

110 ca-, silicon nitride-, and alumina-supported zirconia on silicon nucleates single- and multiwall carb

111 ethyleneimine (PEI) was adsorbed onto porous zirconia particles and cross-linked with 1,4-butanediol

112 about 3-4% (w/w) CDMPC coated on 2.5-micron zirconia particles provide an excellent compromise betwe

113 PBD-coated zirconia particles with six different carbon loads (0.25

114 ition of polyethyleneimine (PEI) onto porous zirconia particles, followed by cross-linking with a nov

115 ven after impingement with yttria-stabilized-zirconia particles, or exposure to ultraviolet light and

116 Polybutadiene-coated zirconia (PBD-ZrO2) is very useful for reversed-phase se

117 decylsilane (ODS) and a polybutadiene-coated zirconia (PBD-ZrO2) phase was used to separate nine anti

118 bonded silica (ODS) and polybutadiene-coated zirconia (PBD-ZrO2) phases.

119 ecially with respect to polybutadiene-coated zirconia (PBD-ZrO2).

120 Our work explores the use of EDTPA-modified zirconia (PEZ) for its potential use as a high-performan

121 othesis, we cemented flat porcelain-veneered zirconia plates onto dental composites and cyclically lo

122 graded structures by infiltrating glass into zirconia plates, resulting in improved aesthetics and di

123 graded structures by infiltrating glass into zirconia plates, with resulting diminished modulus in th

124 n of damage evolution in a transparent glass/zirconia/polycarbonate trilayer, post mortem damage eval

125 ted alumina and yttria-stabilized tetragonal zirconia polycrystal (Y-TZP).

126 Y-TZP (yttria-stabilized tetragonal zirconia polycrystal) is the most widely used variant.

127 based resins to yttria-stabilized tetragonal zirconia polycrystals (Y-TZP) and further investigated t

128 umn packed with 3 microns polystyrene-coated zirconia porous particles, long chain alkylphenones were

129 The surface of zirconia, previously sintered but not rehydroxylated, pr

130 nge phase by amination of polystyrene-coated zirconia (PS-ZrO2) are described.

131 ographic selectivities of polystyrene-coated zirconia (PS-ZrO2) have been investigated in detail by m

132 ase in the resistance to radial cracking for zirconia relative to alumina and for alumina relative to

133 t of currently available and next-generation zirconias, representing a concerted drive toward greater

134 on high-translucent monolithic full-contour zirconia restorations, which have become extremely popul

135 coverage high-strength ceramic or monolithic zirconia restorations.

136 Additionally, zirconia revealed a statistically significant reduction

137 Zirconia's hard Lewis acid sites can be chromatographica

138 is addded to ZrO(2) to selectively passivate zirconia's strong Lewis acidic sites and weaken Bronsted

139 Just as with silica-based phases, zirconia's surface chemistry significantly influences th

140 Zirconia's surface prior to coating was investigated by

141 strong interactions of hard Lewis bases with zirconia's surface.

142 conditions of water with a yttria-stabilized zirconia sensor in a titanium flow reactor.

143 f porcelain-veneered zirconia and monolithic zirconia served as controls.

144 Zirconia showed a statistically significant reduction in

145 Control data were obtained on zirconia specimens without infiltration and on crowns ve

146 Glass-infiltrated dense zirconia structures can now be produced with esthetic qu

147 he CeO(2) thin film on an yttrium-stabilized zirconia substrate using a simulated amorphization and r

148 were epitaxially grown on yttria-stabilized zirconia substrates and have lattice constants that are

149 n grown on both LaAlO3 and yttria-stabilized zirconia substrates using RF magnetron sputtering.

150 er, Lewis acid/base interactions between the zirconia support and the proteins, which can significant

151 Clinically, zirconia-supported all-ceramic restorations are failing

152 VI) oxide powder and comparable to that of a zirconia-supported analogue (Mo-ZrO2) prepared in a simi

153 Zirconia-supported tungsten oxide (WO(x)/ZrO(2)) is cons

154 reviously described alkali-stable PEI-coated zirconia supports cross-linked with 1,10-diiododecane.

155 In contrast to zirconia supports modified with small anionic species, t

156 ly, we have demonstrated that a graded glass-zirconia surface possesses excellent resistance to occlu

157 The multitude of water interactions with the zirconia surface results in the complex but highly order

158 ontact fatigue response of this graded glass-zirconia surface with external esthetic glass.

159 nd platinum-functionalized yttria-stabilized zirconia surfaces is demonstrated.

160 latform for modeling catalysis by tungstated zirconia surfaces.

161 Fracture in the porcelain/zirconia system was limited to surface damage in the ven

162 nd strength with very high flaw tolerance of zirconia/Ta composites.

163 Zirconias, the strongest of the dental ceramics, are inc

164 re observed in the coarse glass-ceramics and zirconia; the medium glass-ceramics and alumina exhibit

165 red by reinforcing them with nanocrystalline zirconia, thus improving their oil-adsorption capacity;

166 ompare PEZ with inorganic phosphate-modified zirconia to show increased efficiency, as well as unique

167 e sites responsible for the high affinity of zirconia toward certain classes of anions.

168 and fracture relative to porcelain-veneered zirconia, while providing necessary esthetics.

169 Modification of zirconia with EDTPA provides a "biocompatible" stationar

170 fluorite-structured oxides such as ceria and zirconia, with application for solid oxide fuel cells.

171 crowns is high relative to that of veneered zirconia (Y-TZP) and comparable with that of metal ceram

172 ceramic microtubes made of yttria stabilized zirconia (YSZ) are presented, which are conditioned for

173 ent is mainly based on the yttria-stabilized zirconia (YSZ) electrolyte.

174 perties of polycrystalline yttria-stabilized zirconia (YSZ) have been studied using FT-Raman spectros

175 en grown on (111)-oriented yttria-stabilized zirconia (YSZ) substrates by off-axis sputtering followe

176 in a bicrystal of yttria (9% mol) stabilized zirconia (YSZ), an emblematic oxide ion conductor.

177 s mechanism in nanograined Yttria Stabilized Zirconia (YSZ), associated with the observation that the

178 in separate thin films of yttria-stabilized zirconia (YSZ), CeO(2), and TiO(2).

179 LD]) and a dense sintered yttrium-stabilized zirconia (YZ) were obtained from the literature and inco

180 We report that nanoparticulate zirconia (ZrO(2)) catalyzes both growth of single-wall a

181 phate (OP) pesticides and nerve agents using zirconia (ZrO(2)) nanoparticles as selective sorbents is

182 of the products of the elimination process, zirconia (ZrO2) powder is a kind of biocompatible materi

183 Experimental disks made of titanium (Ti) or zirconia (ZrO2) with a machined (M) or a sandblasted (SL