ライフサイエンスコーパス: alumina

1 dation on single Pd atoms supported on theta-alumina.

2 so displayed good activity when supported on alumina.

3 lity of liquid sodium on the surface of beta alumina.

4 oly(1-->4-beta-glucan) (beta-glu) strands on alumina.

5 trum of hydroxyl groups in a sample of alpha-alumina.

6 -33 times less expensive than with activated alumina.

7 on of catalysis materials such as mesoporous alumina.

8 pically observed in the "activation" step of alumina.

9 erties of "activated" (thermally pretreated) alumina.

10 HCO(3) in contrast with non-nanoporous alpha alumina.

11 na was found to be similar to that of powder alumina.

12 in dysprosium (Dy)- and lutetium (Lu)-doped alumina.

13 s tightly packed with silica gel followed by alumina.

14 orber consisting of mirror-backed nanoporous alumina.

15 electrodes which are separated by 5 nm thick alumina.

16 incorporation of pH indicators to MCM-41 and alumina.

17 ally allocated to intracameral injections of alumina 0.2 mug, alumina 20 mug, copper sulfate 0.4 mug,

18 intracameral injections of alumina 0.2 mug, alumina 20 mug, copper sulfate 0.4 mug, copper sulfate 2

19 kness and air-filling fraction of nanoporous alumina, according to the Maxwell-Garnet mixture theory,

20 chromatography; the use of deactivated basic alumina (activity IV) afforded high yield and purity.

21 ts from modification of binding sites on the alumina, adjacent to the particles.

22 s focused into a flux of helium charged with alumina aerosols of a few micrometers diameter.

23 Further discs were alumina-air-abraded.

24 We showed that alumina (Al(2)O(3)) overcoating of supported metal nanop

25 shock experiments (A. Rode, unpublished) on alumina (Al2O3) have shown non-equilibrium decomposition

26 on decorated graphene oxide (GO) sheet with alumina (Al2O3) nanocrystals.

27 layer deposition (ALD) of titania (TiO2) and alumina (Al2O3) on Ni-rich FCG NMC and NCA active materi

28 actors, the protocol of adsorbing enzymes to alumina (Al2O3) xerogel modified PDMS surface was demons

29 atoms supported on an inert substrate, theta-alumina (Al2O3), in the presence of stoichiometric oxyge

30 rst-principles calculations, the activity of alumina alpha-Al2O3(0001) surface toward formation of ph

31 3) adsorbed on Bronsted superacidic sulfated alumina (AlS).

32 al dipolar correlation spectra on mesoporous alumina, an advanced material with potential industrial

33 Alumina and copper sulfate did not cause clinically mean

34 ions, Zn-Al LDH precipitates formed on gamma-alumina and corundum but not on less soluble minerals su

35 calibration-free LIBS measurements of solid alumina and glass and promote compositional analysis of

36 yl)tetrabenzoic acid (H4TCPP), to react with alumina and make MOF [Al2(OH)2TCPP] enclosures around Ag

37 iant phase are synthesized by coextrusion of alumina and nickel oxide.

38 -pyridine complex in MeCN and purified using alumina and quaternary methyl ammonium solid-phase extra

39 lly friendly and convenient, indicating that alumina and stannia are suitable for the applications by

40 e nature of the interface between silica and alumina and the atomic structure of the catalytically ac

41 M)-fabricated high-strength ceramics-namely, alumina and zirconia-are widely accepted as reliable alt

42 en limited to metal oxides, e.g., silica and alumina, and organic aerogels, e.g., resorcinol/formalde

43 ytic properties of Fe impregnated on silica, alumina, and titania nanoparticles (as prototypical mine

44 Alumina- and stannia-based hollow fibers were synthesize

45 ucture and nitrogen-doped graphene layers on alumina are obtained by pyrolysis of Co(OAc)2/phenanthro

46 Nanometre-sized particles of transition (t)-aluminas are important for the fabrication of high-quali

47 le supported atoms on inert substrates (e.g. alumina) are limited to adatoms and cations of Pt, Pd, a

48 ctionality arises from the use of mesoporous alumina as an inert scaffold that structures the absorbe

49 m-sulfur battery using K(+) -conducting beta-alumina as the electrolyte to separate a molten potassiu

50 ct by first principles a phase transition in alumina at approximately 3.7 Mbar and room temperature f

51 tion/precipitation on gamma-Al(2)O(3) (gamma-alumina) at pH 7.5 using extended X-ray absorption fine

52 were much less susceptible to fracture than alumina, attributable to a relatively high strength and

53 The binding of this ligand to alumina-based, hydroxyapatite-based, and calcium phospha

54 These results demonstrate that sodium-beta alumina batteries can be operated at much lower temperat

55 or hydrolysis of grafted beta-glu strands on alumina being 70 kJ/mol relative to 87 kJ/mol on silica.

56 The alumina-blasting surface presented the highest average s

57 Five implant surfaces were evaluated: 1) alumina-blasting, 2) biologic blasting, 3) plasma, 4) mi

58 le blasting media (microblasted RBM), and 5) alumina-blasting/acid-etched (AB/AE).

59 1)) in the neat perovskite and in perovskite/alumina blends; almost balanced electron and hole mobili

60 The alumina blocking layer was found to contribute to the no

61 NH2-functionalized, and -SO3H-functionalized alumina but not on -COOH- and -PO3H2-functionalized part

62 ell-Garnet mixture theory, a large-area dark alumina can be made with excellent photothermal properti

63 Organized macroporous-mesoporous alumina can be obtained via a dual-templating approach.

64 assed through a cation exchange resin and an alumina cartridge, followed by saline elution.

65 h isotonic saline, passing through 3 neutral alumina cartridges and a sterilizing filter.

66 vated pressures (e.g., 36 bar) over a silica/alumina catalyst to produce a gas stream composed of equ

67 y active and well-structured nano-mesoporous alumina catalysts/supports from aluminum foil waste and

68 2O3 depends on the activation temperature of alumina; catalysts activated at or above 500 degrees C c

69 The dehydroxylated alumina catalyzes the conversion of phenol into its phen

70 ent of rigid PIM-1 in the channels of anodic alumina causes reduction of small-scale mobility in poly

71 We show the chemical functionalisation of alumina ceramic microfiltration membranes (0.22 mum pore

72 Bioinspired "brick-and-mortar" alumina ceramics containing a nickel compliant phase are

73 ion ( TIT) in particular, of these submicron alumina ceramics has been examined with the Rayleigh-Gan

74 ties of a new class of submicron grain-sized alumina ceramics relative to the current state-of-the-ar

75 findings have shown that for polycrystalline alumina ceramics, an average grain size <1 microm couple

76 mportant for the fabrication of high-quality alumina ceramics.

77 lyte), depending on whether the electrode is alumina coated.

78 tory on the basis of cryoadsorption on short alumina-coated porous layer open tubular (PLOT) columns.

79 um nanoparticles on a carbon surface with an alumina coating for passivation of carbon defect sites.

80 hium peroxide with grain boundaries, and the alumina coating preventing electrolyte decomposition on

81 port on the synthesis of unoxidized graphene/alumina composite materials having enhanced toughness, s

82 ness three or more times higher than that of alumina, consistent with significant extrinsic toughenin

83 lysts prepared by grafting CH3ReO3 on silica-alumina contain two types of spectroscopically distinct

84 uss two quantitative models to determine the alumina content from the Raman spectra of the molten NaF

85 aches are applied to determine both the COx (alumina content) and the CR (NaF/AlF3 molar ratio) by Ra

86 liquid-feed flame spray pyrolysis of nano-t-aluminas converts them to dispersible 30-80 nm alpha-Al(

87 A coarse-grained alumina could also reach a translucency level comparable

88 U(VI) presorbed to mesoporous and nanoporous alumina could not be released by extended (2 week) extra

89 Porcelain-veneered alumina crown restorations often fail from bulk fracture

90 neficial in the design of fracture-resistant alumina crowns.

91 Here, we demonstrate how a nanometerthick alumina deposition inside such a cavity can be used to g

92 m, in which transport of silver ions through alumina dielectric leads to bias-induced nucleation and

93 e formation of an isolating amorphous silica alumina envelope.

94 leanup co-sorbents: florisil, silica, silica/alumina, Envi Carb, Envi-Carb-II/PSA, SAX/PSA, Envi-Carb

95 e of the core is coated with a thin layer of alumina (Fe3O4@Al2O3 MNPs).

96 aphite punches, which are protected from the alumina fiber film by a graphite foil.

97 eved through the insertion of a film made of alumina fibers between the graphite die and the graphite

98 minum alloy grown from Mo(CO)(6) on a planar alumina film formed on a Mo(100) single crystal in ultra

99 w composite membranes based on porous anodic alumina films and polymer of intrinsic microporosity (PI

100 Here, we describe sol-gel-beta-alumina films as transistor gate dielectrics with soluti

101 rmed by atomic layer deposition of ultrathin alumina films on a lithographically patterned silicon wa

102 ively after atomic layer deposition (ALD) of alumina followed by crushing showed significantly improv

103 structure and phase composition of Ln-doped alumina for emerging applications.

104 ely on thermally grown oxide (TGO), commonly alumina, for corrosion protection.

105 ecular ion intensity was optimal with porous alumina formed from aluminum films of approximately 600-

106 Like other alumina formers, the oxidation kinetics follow a cubic t

107 f ordered hexagonal mesopores throughout the alumina framework.

108 d hematite (alpha-Fe2O3) increased and gamma-alumina (gamma-Al2O3) decreased the Hg(0) production rat

109 Reactions of 8b-d with basic alumina gave mixtures of (E)- (13) and (Z)-(10-phenoxath

110 the surface of dehydrated, amorphous silica-alumina generates a highly active, supported catalyst fo

111 In contrast, at pH 5.5, only gamma-alumina-GPS-Zn ternary surface complexes formed regardle

112 Formation of gamma-alumina-GPS-Zn ternary surface complexes was further sug

113 Lanthanide (Ln(3+)) doping in alumina has shown great promise for stabilizing and prom

114 Grafted beta-glu strands on alumina have a 9-fold higher hydrolysis rate per glucan

115 polycrystalline membranes were fabricated on alumina hollow fibers using an in situ solvothermal synt

116 human breast milk samples were used to apply alumina hollow fibers, as a proof of concept.

117 ft followed the order: silica > iron oxide > alumina in 10 mM NaCl at pH 4.0.

118 nd phenoxathiin (PO) when treated with basic alumina in MeCN solution.

119 s are greatly improved by the use of neutral alumina in place of silica for product purification.

120 Nanoporous alumina in the biosensor device generates a high density

121 garnet electrolyte surface and the lithiated-alumina interface allows effective lithium ion transport

122 Re2O7 supported on gamma-alumina is an alkene metathesis catalyst active at room

123 Nickel supported on silica-alumina is an efficient and reusable photocatalyst for t

124 due is the alkaline byproduct generated when alumina is extracted from bauxite ores and is commonly d

125 Because alumina is used as window material in shock-wave experim

126 ypically alpha-Al(2)O(3) nucleation within t-aluminas is sporadic rather than uniform, leading to exa

127 In this study, Ln-doping (400 ppm) of the alumina lattice crucially delays the onset of phase tran

128 ng mechanisms for phase stabilization of the alumina lattice is indispensable.

129 n the vacant octahedral locations within the alumina lattice, where complete conversion into the ther

130 position (ALD) is used to deposit a sub-1-nm alumina layer on silver film-over-nanosphere (AgFON) sub

131 le anodizing process, which yielded a porous alumina layer with pores exhibiting a mean diameter rang

132 the confluence of the silica gel layer with alumina layer.

133 Bulk fracture, observed in veneered alumina layers, was not found for zirconia.

134 The addition of lanthanum oxide to the alumina, long known for its ability to improve alumina s

135 into the matrix of magnesio aluminate spinel-alumina (MA-A) via infiltration of a porous preform fabr

136 auxite residue is a high volume byproduct of alumina manufacture which is commonly disposed of in pur

137 prepared by argon plasma etching through an alumina mask.

138 ering of Si0.8Ge0.2 on highly ordered porous alumina matrices.

139 y, the newly developed submicron grain-sized alumina may be considered a suitable material for dental

140 For the high-dose alumina, mean inflammatory grades peaked at 6 to 9 hours

141 f alkylidenecycloalkanone followed by acidic alumina-mediated regioselective ring expansion of the cy

142 At very high temperatures, yttria-alumina melts show a first-order transition, previously

143 lm or within the pores of Anodisc nanoporous alumina membrane as a densely packed array of poly-MTAPc

144 pesticide sensor comprising of a nanoporous alumina membrane integrated with printed circuit board p

145 scribed the use of a small and thin piece of alumina membrane, 60 mum thick and 13 mm in diameter as

146 on by a monolithically integrated nanoporous alumina membrane, which can support pressure differences

147 as thin films and within the pores of anodic alumina membranes (AAMs), respectively.

148 -active nanoporous substrate based on porous alumina membranes decorated with mixed nanoclusters comp

149 wires are traditionally fabricated in anodic alumina membranes using electrodeposition, and this tech

150 Porous alumina membranes were employed as model chromatographic

151 ylindrical Au-Ru rods in the pores of anodic alumina membranes, dissolution of the template membrane,

152 The relative affinity of analytes for alumina-modified AgFON substrates can be determined by t

153 rmine the saturation binding capacity of the alumina-modified AgFON surface.

154 monstrate that a proper control of the gamma-alumina morphology is a strategic lever for a molecular-

155 degrees C for 24 h and then cleanup with an Alumina-N SPE cartridge.

156 scopy (RIfS) combined with nanoporous anodic alumina (NAA) platforms when detecting different analyte

157 Hollow-tube alumina nanolattices were fabricated using two-photon li

158 We discovered that hollow-tube alumina nanolattices with 3D kagome geometry that contai

159 Formation of so-called hydration layer on alumina nanoparticles in water was hypothesized, but nev

160 d nanoprobes (Gal-1 antibodies conjugated to alumina nanoparticles through silane modification) that

161 K result in the formation of a 1.5 nm thick alumina nanosheet underneath graphene.

162 d-phase extraction with MgSO4, PSA, C18, and alumina-neutral.

163 In comparison to pure alumina, nickel aluminum oxide samples exhibited larger

164 Catalytic reduction (5% Rh/alumina) of 2'-deoxyuridine, followed by reduction with

165 wo compartments separated by either a porous alumina or polycarbonate membrane as a model system, dif

166 small amounts activate platinum adsorbed on alumina or silica for the low-temperature water-gas shif

167 onsisting of glass veneers epoxy-joined onto alumina or zirconia cores, all bonded to a dentin-like p

168 cking were observed for specimens containing alumina or zirconia cores.

169 erm studies indicate that porcelain-veneered alumina or zirconia full-coverage crowns and fixed denta

170 Atomic layer deposition (ALD) of an alumina overcoat can stabilize a base metal catalyst (e.

171 The alumina overcoat initially covers the catalyst surface c

172 hile presenting the surface chemistry of the alumina overlayer, a commonly used polar adsorbent in ch

173 , ZnO nanoparticle assemblies with ultrathin alumina overlayers, dramatically enhance durability of a

174 inner walls (200 nm diameter) of an anodized alumina oxide filter membrane (AAO).

175 Porous anodic alumina (PAA) films are widely used as templates for fun

176 tailoring the surface chemistry of colloidal alumina particles (d50 = 180 nm) with amino (-NH2), carb

177 us grit sizes or grit-blasting with airborne alumina particles, were subjected to accelerated aging t

178 reasing gradually the formation of spherical alumina particles.

179 enched to induce compressive stresses in the alumina passivation shell surrounding Al core.

180 composition ratios between alpha- and theta-alumina phases are studied using a combination of solid

181 chemically functionalized nanoporous anodic alumina photonic films (NAA-PFs) and reflectometric inte

182 d that gallium was produced from 8 to 21% of alumina plants in 2011.

183 structures by infiltrating glass into dense alumina plates, resulting in a diminished modulus at the

184 Finally, alumina polishing of lapped, NDC free, freestanding, BDD

185 micro-truss and -shell structures made from alumina-polymer composite.

186 gnal intensity was examined as a function of alumina pore depth, pore width, and gold layer thickness

187 cle size occurs with both films deposited on alumina powder and nanoparticles stabilized by polyelect

188 )-Pd(II) complexes and poly(ethylenimine) on alumina powder followed by reduction of Pd(II) with NaBH

189 Pure alumina powder has been used without any binder phase, e

190 It is significantly lower than the pzc of alumina powder.

191 syn-addition via pathway a, while the use of alumina provided access to the anti-adduct.

192 e are produced globally as a by-product from alumina refineries.

193 ontaneous colonization of a bauxite residue (alumina refining tailings) deposit by local vegetation i

194 ailings material generated as a byproduct of alumina refining), to which a diverse microbial inoculum

195 l min)(-1) for hematite, goethite, and gamma-alumina, respectively.

196 verage of aluminum and silicon on silica and alumina, respectively.

197 nd optical optimization of nanoporous anodic alumina rugate filters (NAA-RFs) for real-time and label

198 serum albumin by combining nanoporous anodic alumina rugate filters (NAA-RFs) modified with human ser

199 heating rates of 5 degrees C min(-1) and an alumina sample holder improve the efficiency of the dryi

200 nolattices; (ii) recoverability, with hollow alumina samples recovering up to 98% of their original h

201 Sodium beta-alumina (SBA) has high two-dimensional conductivity, owi

202 ides, MoAlB forms a dense, mostly amorphous, alumina scale when heated in air.

203 particle layer into a dense amorphous silica-alumina shell further reduces the mass transport to the

204 ion of core-shell particles (silica core and alumina shell) to low-density framework types and their

205 Size-dependent strengthening of alumina shells has been observed, particularly when appl

206 Nano-t-aluminas should provide access to dense nano/submicromet

207 technologically important materials such as alumina, silica, and copper metal.

208 Although the alumina-silica system has been intensely studied, the ef

209 ience approach using four well-defined alpha-alumina single crystal surfaces (C (0001), A (1120), M (

210 as reducing the content of light-scattering alumina sintering aid or incorporating a component of op

211 bilization of the unstable enzyme, including alumina sol-gel encapsulation, physisorption to PDMS cha

212 ogen activator was entrapped within a porous alumina sol-gel film with a subsequent deposition on a p

213 ood commodities with methanol, cleaned up by alumina-SPE column, and then determined by HPLC-MS/MS.

214 ve field transmitted through randomly packed alumina spheres--can be decomposed into a sum of the pat

215 umina, long known for its ability to improve alumina stability, is found to also help in the stabiliz

216 ogel consisting of approximately 10 nm-thick alumina strands, spaced by approximately 100 nm, and ali

217 The Si0.8Ge0.2 film replicated the porous alumina structure resulting in nano-meshed films.

218 membrane was grown and supported on a porous alumina substrate using a solvothermal crystallization m

219 the migration from the dissolution of gamma-alumina substrate.

220 of 1-hexanoic acid most likely occurs on the alumina support, and probably results from modification

221 s phase, deposited on an ultrathin amorphous alumina support, and tested as catalysts experimentally

222 Alumina-supported Cu(II) efficiently catalyzes selenylat

223 position of CH4 gas on a specially activated alumina-supported Fe:Mo catalyst.

224 reproducible synthesis of ordered mesoporous alumina-supported materials for various applications whe

225 ide was demonstrated by preparation of other alumina-supported metal oxides such as MgO, CaO, TiO 2,

226 The one-pot synthesis of alumina-supported metal oxides via self-assembly of a me

227 the liquid/solid interface of optically flat alumina-supported palladium nanoparticle surfaces prepar

228 e particle size controls the CO/CO2 ratio on alumina-supported Pd, demonstrating the potential applic

229 gamma-Alumina-supported single-atom alloy nanoparticle catalys

230 observe that silica-, silicon nitride-, and alumina-supported zirconia on silicon nucleates single-

231 roximately 3.5-nanometer Ag nanoparticles on alumina supports can catalyze this reaction with only a

232 e membranes comprising crumpled nanofilms on alumina supports provided high retention of solutes, wit

233 ial penetration of polymer into the pores of alumina supports takes place giving rise to selective po

234 thesized on porous stainless steel and alpha-alumina supports using a seeded growth method.

235 ing site-isolated secondary amines on silica-alumina supports.

236 ically active on industrially relevant gamma-alumina supports.

237 te that protonation and deprotonation of the alumina surface dominate at low and high pH, respectivel

238 s and conformations of the substrates at the alumina surface through high-resolution measurements of

239 on were partitioned between the solution and alumina surface to quite varying degrees.

240 A gold coated nanoporous alumina surface was used for dual ionization mode mass s

241 I mass spectrometry (MS) from the nanoporous alumina surface were compared with conventional electros

242 fulvic acid (SRFA) during its sorption at an alumina surface, taken as a model for surfaces of natura

243 ively yields monomeric SiO(x) species on the alumina surface.

244 mingled palladium and lanthanum on the gamma-alumina surface.

245 s, and the desorption of rhodamine B from an alumina surface.

246 ructural analogies between alpha- and gamma- alumina surfaces allow us to bridge the material gap wit

247 1-hexanoic acid adsorbs to both ALD-prepared alumina surfaces and alumina surfaces with palladium nan

248 ons between carbon-containing substrates and alumina surfaces is of paramount importance to industria

249 bs to both ALD-prepared alumina surfaces and alumina surfaces with palladium nanoparticles, that were

250 In this study, nitrate adsorbed on alumina surfaces, a surrogate for mineral dust aerosol,

251 bs with conformational order on ALD-prepared alumina surfaces, but on surfaces with palladium particl

252 red pathways for the adsorption of phenol on alumina surfaces, corroborating the role of particulate

253 FT) calculations, we show that on silica and alumina surfaces, molecular aluminum and silicon precurs

254 high reactivity of partially dehyxdroxylated alumina surfaces.

255 of conductive polymer nanotubes in a porous alumina template using poly(3,4-ethylenedioxythiophene)

256 meter, pitch, neck) was achieved through the alumina template, with pore diameters ranging from 294 +

257 d by electrochemical polymerization using an alumina template.

258 velop during isothermal growth conditions in alumina TGO formed on a FeCrAlY alloy.

259 s to a hydrolysis rate per grafted center on alumina that is 2.7-fold more active than on silica.

260 ore-shell subunits on silicon-functionalized alumina that was recently reported has created renewed i

261 and R (1102) planes) as surrogates for gamma-alumina (the industrial support) in order to discriminat

262 recursor to form 2 nm Ni(0) nanoparticles on alumina, the commonly used support in DRM.

263 rt can be mitigated through the Mg-doping of alumina, thereby increasing significantly the stability

264 Alumina thickness is precisely controlled from 0.1 to 3

265 rformed on Au particle ensembles prepared on alumina thin films suggest that the molecular ligands ar

266 e overcoated palladium NPs with 45 layers of alumina through an atomic layer deposition (ALD) process

267 greater than other reported anodized porous alumina, typically semi-transparent at similar wavelengt

268 and diaryl dichalcogenides on the surface of alumina under ball-milling without any solvent or metal.

269 of the photocatalytic activity of Ni/silica-alumina under solar light derives from the visible light

270 hich indicated the glyphosate binds to gamma-alumina via a phosphonate group, bridging the mineral su

271 GSSG is suggested to bind to -SO3H-modified alumina via the primary amino groups of both GS moieties

272 The pzc of amorphous alumina was found to be similar to that of powder alumin

273 irmed that U(VI) presorbed to non-nanoporous alumina was rapidly and completely reduced to nanopartic

274 s reduction of U(VI) presorbed to nanoporous alumina was slow and incomplete (<5% reduction after 1 w

275 The flexural strength of the aluminas was determined with the 4-point bending test.

276 The strength of these submicron grain-sized aluminas was significantly higher than that of the cubic

277 ated separately with silica, iron oxide, and alumina were applied in quartz crystal microbalance with

278 (GPS) on Zn sorption/precipitation on gamma-alumina were investigated using a batch technique, Zn K-

279 ically disposed silver nanowires embedded in alumina were shown to be capable of conducting plasmons

280 te adsorbed to boehmite, corundum, and gamma-alumina were significantly different.

281 contrast ratio ( CR) of the newly developed aluminas were measured with a reflectance spectrophotome

282 (GS) moieties onto native and -NH2-modified alumina, whereas GSSG is suggested to bind to -SO3H-modi

283 rmal stability to oxides, such as silica and alumina, which are not otherwise stable at elevated temp

284 rticular example is Pt clusters deposited on alumina, which have been shown to dehydrogenate hydrocar

285 acquire a chloride ligand from the modified alumina while donating an oxo ligand to the support.

286 However, silica-alumina with a high (10 wt %) Re loading is no more acti

287 Loading alumina with a sparse concentration of Ln-dopants sugges

288 old higher specific activity than the parent alumina with identical selectivity.

289 However, doping alumina with Ln elements is generally accompanied by for

290 %) Re loading is no more active than silica-alumina with low (1 wt %) loading, while CH3ReO3 on sili

291 f our results on all high-pressure phases of alumina with shock data suggests the presence of two pha

292 The reaction of gamma-alumina with tetraethylorthosilicate (TEOS) vapor at low

293 this approach is demonstrated on mesoporous alumina with the acquisition of well-resolved DNP surfac

294 rect visualization of aqueous suspensions of alumina with the fluid cell in situ.

295 have shown non-equilibrium decomposition of alumina with the formation of free Al and a mysterious t

296 d catalysts (i.e., Pd on activated carbon or alumina) with respect to nitrite reduction activity and

297 flow conditions on the SAA NPs supported on alumina without activity loss in the presence of CO.

298 isorption to PDMS channels with, and without alumina xerogel modification, were compared to build a m

299 romoacetophenones in the presence of neutral alumina yields 2-substituted benzo[b]furans with complet

300 f these latter compounds promoted by neutral alumina yields the corresponding 3-substituted benzo[b]f