ライフサイエンスコーパス: Al

1 Al(3)O(4)(+) exhibits a cone-like structure with a centr

2 Al(IV)-2 sites result either from framework crystallizat

3 Al@Al is fully wetted by a 4 m potassium bis(fluorosulfo

4 wavelength of 414.234 (Fe I) nm and 396.054 (Al I) nm, and the kurtosis of spectra at wavelength rang

5 Ca(12)Ga(14)O(33) analogue compared to Ca(12)Al(14)O(33) synthesized using the same wet chemistry tec

6 In naturally occurring Ca(12)Al(14)O(33), the mineral mayenite, these cages are occup

7 that the compound is isostructural to Ca(12)Al(14)O(33,) however, with a significantly larger lattic

8 Focusing on Li(x)Ni(0.8)Co(0.15)Al(0.05)O(2) as a model compound, we use operando synchr

9 Relative to other ultraporous MOFs, NU-1501-Al exhibits concurrently a high gravimetric Brunauer-Emm

10 rformances for hydrogen and methane: NU-1501-Al surpasses the gravimetric methane storage U.S. Depart

11 rd the trithiocarbonate species [K(OEt(2) )][Al(NON(Dipp) )(CS(3) )] 1 or the ethenetetrathiolate com

12 olymorphs of the feldspars anorthite (CaSi(2)Al(2)O(8)), albite (NaAlSi(3)O(8))(,) and microcline (KA

13 se of atenolol was achieved from FAU (SiO(2):Al(2)O(3) = 80:1) into phosphate buffer for 24 h followe

14 , such as those observed at different SiO(2):Al(2)O(3) ratios.

15 ation at the Si(II) atom with [H(OEt(2))(2)][Al{OC(CF(3))(3)}(4)] induces formal oxidation, and the c

16 Na(+), K(+), Mg(2+), Ca(2+), Mn(2+), Fe(2+), Al(3+), Ni(2+), Cu(2+), Zn(2+), Co(2+), Pb(2+) and Ru(3+

17 characteristic features observed in both (27)Al and (71)Ga NMR spectra result from both the deviation

18 ix-fold-coordinated aluminum observed by (27)Al NMR in C-A-S-H samples.

19 al dynamic nuclear polarization enhanced (27)Al and (29)Si solid-state NMR experiments.

20 d with computational modeling, extensive (27)Al MQMAS experiments at multiple field strengths, and (1

21 a variety of nuclei ((1)H, (13)C, (19)F, (27)Al, and (93)Nb) with a range of one- and two-dimensional

22 Ultrahigh field (27)Al{(1)H} 2D correlation NMR experiments demonstrate that

23 We notably assign a narrow (27)Al NMR signal at 5 ppm to the silicate-bridging [AlO(2)(

24 eferences, we combine solid-state (17)O, (27)Al, and (71)Ga magic angle spinning (MAS) NMR spectrosco

25 The sharp (27)Al and (71)Ga resonances arise from dopants located at a

26 A correlation between the size of the (27)Al/(71)Ga quadrupolar coupling and the distortion of the

27 mmercially available alane amine adduct (H(3)Al.NMe(2)Et) in toluene resulted in the formation of a c

28 gnetic Al addition in the CoFeNi(0.5)Cr(0.5)-Al(x) (x: 0, 0.5, 1, and 1.5) complex concentrated alloy

29 l characterisation of the CoFeNi(0.5)Cr(0.5)-Al(x) composition and attempt to relate it to the interf

30 ores how rapid formation of ettringite [Ca(6)Al(2)(SO(4))(3)(OH)(12).26(H(2)O)], a common mineral for

31 hermal-driven structural ordering in a Ce(65)Al(10)Co(25) metallic glass, and a reverse disordering p

32 sition (DED) manufacturing process of a 7075-Al alloy part.

33 nd N), and lignin composition (inherited (Ad/Al)s and C/V) were not completely consistent in reflecti

34 a dual OSDA and exfoliating agent to affect Al siting and to eliminate the need for postsynthesis ex

35 ths as narrow as 4 nm from arrays of Au, Ag, Al, and Cu NPs.

36 Both alpha-Al dendrites and the silicon particle sizes were signifi

37 simulations of SCN(-) near the neutral alpha-Al(2)O(3)(0001)/H(2)O interface show that the vSFG respo

38 sing large volume fractions of primary alpha-Al dendrites and ultrafine Al-Si eutectic of lamellar mo

39 rfacial electrostatic potential at the alpha-Al(2)O(3)(0001)/H(2)O interface.

40 the concentrations of Mn, Fe, and aluminum (Al) in the soil solution of subsurface samples, whereas

41 oil minerals such as iron (Fe) and aluminum (Al).

42 ss increased with extractable soil aluminum (Al) (r(2) = 0.97; p < 0.1), but Al had no significant re

43 eposition (ALD) of a few-nanometer amorphous Al(2) O(3) layers onto atomically thin single-crystallin

44 st for oxygen vacancies, while the amorphous Al(2) O(3) facilitates the generation and stabilization

45 position, and we include data for SiO(2) and Al(2)O(3) as further examples.

46 role in Earth's history, such as Fe(3+) and Al(3+) .

47 materials, a number of dual-ion battery and Al-ion battery technologies are experiencing booming dev

48 The tendency of Mg-Ca and Al-Fe fouling was observed over the membrane surface.

49 y absorption measurements reveal that Cu and Al enable a favourable Cu coordination environment that

50 et little is known about how reactive Fe and Al minerals affect C cycling in restored wetlands.

51 In upland soils, reactive Fe and Al minerals can contribute to soil C accumulation throug

52 nteractions among soil C and reactive Fe and Al minerals in drained and reflooded wetland soils.

53 s in soils rich in poorly crystalline Fe and Al minerals.

54 (2) dissolution of poorly crystalline Fe and Al oxides by 1 M HCl, releasing P occluded by these oxid

55 g interface charges between the graphene and Al(2)O(3) as compared to use of a 2 nm Al buffer layer.

56 ative addition chemistry involving Al(I) and Al(III) intermediates.

57 monstrated benchmarked against NMC, NCA, and Al-Mg-codoped NMC (NMCAM) of identical Ni content (89 mo

58 morphology of hypereutectic Al-17wt.%Si and Al-20wt.%Si alloys have been investigated.

59 plex coordination interaction between TA and Al(3+).

60 t configuration analysis for the undoped and Al and/or Ga-doped LLZO variants uncovers an interplay b

61 The reactivity of the electron-rich anionic Al(I) aluminyl compound K(2) [(NON)Al](2) (NON=4,5-bis(2

62 ing on biasing the framework Al arrangement (Al-O(-Si-O)(x)-Al, x = 1-3) among CHA zeolites of essent

63 and 8 ML) to achieve the same composition as Al(0.4)Ga(0.07)In(0.53)As quaternary random alloy (RA).

64 zation characteristics of In(0.53)Ga(0.47)As/Al(0.48)In(0.52)As superlattice avalanche photodiodes (I

65 iphosphaarsenium salt, [{(Dipp)(2) P}(2) As][Al{OC(CF(3) )(3) }(4) ].1 1/2 PhMe, is described.

66 ctions from January 2016 to December 2017 at Al Ain Hospital in the United Arab Emirates (UAE).

67 solved HAs and enrichment of HAs adsorbed at Al(2)O(3).

68 bnormally smaller and increased in number at Al-12.2at.%Si, compared with 800 degrees C MS alloys, wh

69 an optical cavity substrate consisting of Au/Al(2) O(3) to enhance its absorption near the bandgap ed

70 ne with BF(3).Et(2)O unexpectedly led to a B/Al metathesis with the preservation of the pincer struct

71 t of this research indicated that SERS based Al-QS could be a suitable candidate for the early diagno

72 ticle growth and ion exchange with the beta"-Al(2) O(3) electrolyte.

73 y correlation strength and direction between Al and base cations, total organic carbon, turbidity, an

74 y results from the complex interplay between Al-mediated lattice distortion (due to its larger atomic

75 of identifying a suitable ligand for binding Al(3+) ion.

76 hene is protected from oxidation enabling BN/Al(2)O(3) layers as thin as 4 nm.

77 (2)O(3) films on epitaxial V(2)O(3) buffered Al(2)O(3) (0001) single crystal substrates.

78 il aluminum (Al) (r(2) = 0.97; p < 0.1), but Al had no significant relationship with litterfall, sugg

79 lyses suggest that the particles enriched by Al tend to agglomerate in a needle-shaped structure.

80 ically, this is driven, at least in part, by Al-O bond formation.

81 total phenolic content in treated plants by Al(2)O(3) NPs compared to the control plants.

82 exagonal lattices, such as those provided by Al(2)O(3)(0001) and (111) oriented cubic perovskites, ar

83 spin surface states, that is proximitized by Al superconducting leads.

84 eneficial for tremor control as published by Al-Fatly et al in 2019.

85 nit cell), but cannot be described solely by Al-Al distance or density.

86 odic table, in particular metals such as Ca, Al, Na, Zn, and Fe and halogens like Cl and F, occurring

87 n the metathetical synthesis of Mg-Al and Ca-Al bonded derivatives.

88 )-containing environment, aluminium cations (Al(3+)) was incorporated into a layered surface film com

89 Certain Al distributions yield rigid arrangements of anionic cha

90 als that can readily intercalate high-charge Al(3+) ions.

91 of pyridine, resulting in a four-coordinate Al.

92 lding units where penta- or hexa-coordinated Al is present.

93 e that this second tetrahedrally coordinated Al site (denoted Al(IV)-2) experiences an increased chem

94 Direct-to-indirect bandgap crossover Al mole fractions for c-phase AlGaN and AlInN alloys are

95 /G ratio, proline, pH, conductivity, Fe, Cu, Al, and Mn values were found in the chestnut honeys.

96 Here we describe Cu-Al electrocatalysts, identified using density functional

97 m bonds with short metal-metal distances, Cu-Al = 2.3010(6) angstrom and Cu-Ga = 2.2916(5) angstrom.

98 mputational studies that suggest that the Cu-Al alloys provide multiple sites and surface orientation

99 thodology for modelling of disorder in delta-Al(2) O(3) and twinning in theta-Al(2) O(3) and show tha

100 formations, including the formation of delta-Al(2) O(3) and theta-Al(2) O(3) .

101 the two different intergrowth modes of delta-Al(2) O(3) have different transformation characteristics

102 tics and that a significant portion of delta-Al(2) O(3) is stabilized with theta-Al(2) O(3) even afte

103 d tetrahedrally coordinated Al site (denoted Al(IV)-2) experiences an increased chemical shift and un

104 ''turn-on" fluorogenic chemosensor to detect Al(3+).

105 cclude with TMAda(+) and stabilize different Al configurations.

106 We identify five distinct Al regimes with different timing of seasonally elevated

107 rk Ga at framework sites comprised of either Al or Ga reveal a site-specific preference for stabilizi

108 Seasonally elevated Al concentrations exceeded the 0.1-0.2 mg L(-1) World He

109 Seasonally elevated Al concentrations may pose a particular threat to freshw

110 with different timing of seasonally elevated Al concentrations.

111 Al, prior to the formation of extraframework Al.

112 ing an aluminum-powder-coated aluminum foil "Al@Al," without any modification of the support surface

113 eversible recognition of monomer 4 and P for Al(3+) was also proved in presence of Na(2)EDTA by both

114 e determination of polar pesticides (fosetyl-Al and its metabolite, phosphonic acid, and ethephon) an

115 lete postsynthetic hydrolysis of a framework Al, prior to the formation of extraframework Al.

116 FI zeolites with tetrahedral extra-framework Al into Al-enriched mesoporous ZSM-5 nanoboxes with low

117 tly use organic SDAs and influence framework Al arrangements.

118 emplate N atoms bind to a specific framework Al site to expand its coordination to the unusual octahe

119 fects of SDA siting on biasing the framework Al arrangement (Al-O(-Si-O)(x)-Al, x = 1-3) among CHA ze

120 ents demonstrate that at least two framework Al(IV) sites with hydroxyl groups can exist in acidic ze

121 The reservoir-free Al@Al half-cell is stable at 1000 cycles (1950 h) at 0.5

122 ctions in acidic deposition, high freshwater Al concentrations continue to threaten acidified ecosyst

123 a metal-organic framework (MOF) built from (Al-OH)(n) secondary building units and a mixture of 2,2'

124 entrations of immobile trace elements (e.g., Al, Fe, Ti) far exceed global riverine and open ocean me

125 gamma-Al(2)O(3) is one of the most widely used catalysts or ca

126 Ag/gamma-Al(2)O(3) is widely used for catalyzing various reaction

127 t average Cu oxidation state of 1+ for gamma-Al(2)O(3)-supported Cu.

128 ndom distribution of oxygen species in gamma-Al(2)O(3).

129 lar supports such as carbon materials, gamma-Al(2)O(3), and zeolite, which is vital to their practica

130 gamma-Al(2)O(3), but not on microsized gamma-Al(2)O(3).

131 ance than the Ag cluster on microsized gamma-Al(2)O(3).

132 erminal hydroxyls existed on nanosized gamma-Al(2)O(3) can lead to single-atom silver dispersion, the

133 ontaneously achieved only on nanosized gamma-Al(2)O(3), but not on microsized gamma-Al(2)O(3).

134 High-temperature treatment of gamma-Al(2) O(3) can lead to a series of polymorphic transform

135 d determination of oxygen structure of gamma-Al(2)O(3) by using two-dimensional (2D) solid-state NMR

136 Understanding the structure of gamma-Al(2)O(3) is essential to tuning its physicochemical pro

137 reveal that the terminal hydroxyls on gamma-Al(2)O(3) are responsible for anchoring Ag species.

138 d anchoring mechanism of Ag species on gamma-Al(2)O(3) remains largely unknown.

139 These factors may include the Pt/gamma-Al(2)O(3) surface interfacial region as one component of

140 selectively removed pdac ligands to generate Al(2)(OH)(OH(2)) sites, which were subsequently triflate

141 and 0.775 for the chemosensor HMBP and HMBP-Al(3+), respectively.

142 The stoichiometric ratio of HMBP-Al(3+) was determined as 1:2 by Job's plot and ESI-MS as

143 cts marketed in Europe: aluminium hydroxide (Al(OH)(3) ) is the most frequently used adjuvant, with m

144 istribution, and morphology of hypereutectic Al-17wt.%Si and Al-20wt.%Si alloys have been investigate

145 Among them, K(i), Al(iii), and Zn(ii) complexes were used for the polymeri

146 lexes were also synthesized, including K(i), Al(iii), Zn(ii), Sn(ii), Ge(ii), and Si(ii/iv).

147 ositively associated with soil C and Fe(II) (Al R(2) = .91; Fe(II): R(2) = .54-.60).

148 (10-240 nm) Si-rich microstructures exist in Al-12.2at.%Si alloy melt, and the large Si-rich microstr

149 e band gap by nearly 1 order of magnitude in Al(2)O(3) (<6 x 10(10) cm(-2)) and in HfO(2) (<3.9 x 10(

150 the disruption of Si-rich microstructure in Al-12.2at.%Si alloy melt at 1100 degrees C.

151 es that the large Si-rich microstructures in Al-12.2at.%Si alloy melt are probably aggregates compris

152 or cognitive dysfunction as was observed in Al-treated animals.

153 em by patterning an elongated epitaxial InAs-Al island embedded in an Aharonov-Bohm interferometer.

154 a tunable anomalous Josephson effect in InAs/Al Josephson junctions measured via a superconducting qu

155 ns of secondary phases (mainly intermetallic Al-Fe-Be) were observed inside grains, along dislocation

156 tes with tetrahedral extra-framework Al into Al-enriched mesoporous ZSM-5 nanoboxes with low silicon-

157 he very small quantities of the investigated Al content.

158 ation/oxidative addition chemistry involving Al(I) and Al(III) intermediates.

159 cage and contain predominantly 6-MR isolated Al sites.

160 [K{Al(NON(Dipp) )}](2) (NON(Dipp) =[O(SiMe(2) NDipp)(2) ](2

161 oxide to afford the oxygen analogue of 3, [K{Al(NON(Dipp) )(O(2) C)}](2) [4](2) containing the hither

162 The dimeric alumoxane [K{Al(NON(Dipp) )(O)}](2) reacts with carbon monoxide to af

163 )] 1 or the ethenetetrathiolate complex, [K{Al(NON(Dipp) )(S(2) C)}](2) [3](2) .

164 In addition to the known Al(IV) at the framework bridging acid site (BAS), a new

165 reased in plants treated with 100-2,500 mg/L Al(2)O(3) NPs.

166 A high mass difference between the light Al and heavy matrix components limits mass interference.

167 ch microstructure in engineering-lightweight Al-12.2at.%Si alloy melt at 1100 degrees C, via melt-spi

168 13 metal beta-diketiminates M(BDI(Dip)) (M = Al or Ga; BDI(Dip) = N,N'-bis(2,6-diisopropylphenyl)pent

169 trinuclear clusters, namely, NU-1501-M (M = Al or Fe).

170 trate, enabled us to prove that the measured Al signal represents the real distribution of Al nanopar

171 lytic activity of the main-group metals (Mg, Al and Ca) in oxygen reduction reaction is severely hamp

172 nce was assessed using 16 variables (Na, Mg, Al, V, Co, Ni, As, Se, Rb, Sr, Mo, Hg, delta(2)H, delta(

173 utilised in the metathetical synthesis of Mg-Al and Ca-Al bonded derivatives.

174 s, but several elements (Ba, Ca, Mg, Sr, Mn, Al, Co, Ni, Se) were marked as characteristic of honey t

175 d shape-controlled synthesis of monodisperse Al nanocrystals remains an open challenge, limiting thei

176 ines in all regimes, and inorganic monomeric Al is projected to exceed the 15 mug L(-1) threshold for

177 s from partially bonded framework (SiO)(4-n)-Al(OH)(n) species that significantly increase catalyst r

178 Understanding cation (H(+) , Li(+) , Na(+) , Al(3+) , etc.) intercalation/de-intercalation chemistry

179 desolvated particles of eight elements (Na, Al, Ag, Sr, Ca, Mg, Fe, and Be) were injected into the c

180 red aluminum and nickel oxide nanoparticles (Al(2)O(3) and NiO NPs) on plant growth, oxidative stress

181 action (likely controlled by nanoparticulate Al and Fe oxyhydroxide minerals) and estuarine processin

182 e and Al(2)O(3) as compared to use of a 2 nm Al buffer layer.

183 In the case of K(2) [(NON)Al(NDipp)](2) (NON=4,5-bis(2,6-diisopropylanilido)-2,7-d

184 h anionic Al(I) aluminyl compound K(2) [(NON)Al](2) (NON=4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-

185 give the Au-C bonded insertion products (NON)Al(X(2)C)AuP(t)Bu(3) (X = N(i)Pr, 4; X = O, 5).

186 C=N stretch region originates from a SCN-H-O-Al complex, suggesting the surface site specificity of t

187 that although O sites in both framework Si-O-Al and Si-O-Si linkages are enriched simply on exposure

188 sure to H(2)(17)O(l), the enrichment of Si-O-Al species is more rapid, with a more uniform framework

189 modifications influence the accommodation of Al(3+) ions.

190 no significant oxidation caused by PE-ALD of Al(2)O(3).

191 enhanced atomic layer deposition (PE-ALD) of Al(2)O(3) on graphene for top gated field effect transis

192 ry widely with the number and arrangement of Al (1-5 per 36 T-site unit cell), but cannot be describe

193 a novel dedicated model sample consisting of Al nanoparticles buried under a 50 nm thick Cu thin film

194 The nanofluid mixture consists of Al(2)O(3) nanoparticles and water, whereas the LFTF mixt

195 centrated and non-protective coordination of Al species can facilitate post-synthetic treatment to pr

196 Atomic layer deposition of Al(2)O(3) prevents NC aggregation and enables applicatio

197 d enable for the first time the detection of Al and H association on a dry HZSM-5 catalyst, i.e., und

198 derived polymer P for specific detection of Al(3+) ions.

199 he chemosensor HMBP for the determination of Al(3+) in real food samples, drinking waters and herbal

200 ) was developed for further determination of Al, Ca, Cr, Cu, Fe, K, Mn, Mo and Ni in rice samples by

201 ested by MIC-DV for further determination of Al, Cr, Cu, Fe, Mn, Sr, and Zn.

202 l signal represents the real distribution of Al nanoparticles and does not originate from the artifac

203 , regimes are distinguished by a gradient of Al-base cation decoupling as Ca and Mg concentration app

204 al variation of Al to quantify the impact of Al on human health, water treatment, and aquatic organis

205 stick-like and dendritic shape inclusions of Al(2)O(3) in steel.

206 Using Ag (220 nm) instead of Al (100 nm) as cathode, the champion PCE was further imp

207 This isomer of Al(2)FeO(4)(+) is predicted to be highly reactive with r

208 ctivities after exposure to 50-2,500 mg/L of Al(2)O(3) NPs and NiO NPs.

209 ificantly increased under 50 and 100 mg/L of Al(2)O(3) NPs or 50 mg/L of NiO NPs treatment, but was s

210 e states on NiO by depositing a monolayer of Al(2)O(3).

211 at 1100 degrees C, via melt-spinning (MS) of Al(1-x)Si(x) (x = 0.03,0.07,0.122,0.2) alloy melts from

212 ith a water-vapor diffusion barrier ~8 nm of Al(2)O(3).

213 edge gap by identifying seasonal patterns of Al and their drivers in 16 rivers across Nova Scotia, Ca

214 nge in structure and gas phase reactivity of Al(3)O(4)(+) upon Fe-substitution, which is correctly pr

215 The gas phase vibrational spectrum of Al(2)FeO(4)(+) is exclusively reproduced by the latter s

216 The electrochemical stability of Al@Al versus planar Al is not related to differences in

217 like "isomorphous substitution" structure of Al(2)FeO(4)(+) to be the most stable one, except for fun

218 tance of understanding seasonal variation of Al to quantify the impact of Al on human health, water t

219 for the epitaxy of CuCrO(2) delafossites on Al(2)O(3) substrates.

220 1)-oriented CuCrO(2) epitaxial thin films on Al(2)O(3) substrates.

221 The present study focuses on Al(0.7)CoCrFeNi, a lamellar dual-phase (fcc + B2) precip

222 cent sensors for selective detection of only Al(3+), due to the challenge of identifying a suitable l

223 lymer P exhibit high selectivity toward only Al(3+) with no interference from other metal ions, havin

224 Soil moisture, organo-Al, and reactive Fe explained most of the variation obse

225 In contrast, reactive organo-Al in drained soils facilitates C storage via aggregatio

226 In drained soils, organo-Al complexes were positively associated with soil C and

227 Sorption to redox-inert aluminum oxide (Al(2)O(3)) was recently found to affect the redox proper

228 romote the formation of 6-MR and 8-MR paired Al arrangements, respectively.

229 ly proportional to the number of 6-MR paired Al sites, quantified by Co(2+) titration.

230 tisation increase is strange as paramagnetic Al addition dilutes the ferromagnetic Fe/Co/Ni additions

231 he change in magnetisation with paramagnetic Al addition in the CoFeNi(0.5)Cr(0.5)-Al(x) (x: 0, 0.5,

232 cally modulate the carrier density in planar Al-doped ZnO (AZO) metasurfaces without any associated t

233 trochemical stability of Al@Al versus planar Al is not related to differences in potassiophilicity (n

234 ) samples before and after sorption to polar Al(2)O(3) and a nonpolar sorbent (DAX-8 resin).

235 ed by the intercalation of highly polarising Al(3+) ions should be considered when designing new elec

236 heory, in contrast, predicts a less reactive Al(3)O(4)(+)-like "isomorphous substitution" structure o

237 search highlights the complexity of seasonal Al dynamics and the importance of understanding seasonal

238 ing about the timing and drivers of seasonal Al fluctuations.

239 ion by X-ray crystallography reveals a short Al-N distance, which is thought primarily to be due to t

240 reaction, using a Cu-CHA catalyst with a Si/Al ratio of 15 and 2.6 wt% Cu, by X-ray absorption spect

241 eolites of essentially fixed composition (Si/Al = 15).

242 ctivity of their sub-nanometer pores, the Si/Al ratio of the anionic framework, and the charge-balanc

243 t has been discovered in a relatively simple Al(0.3)CoFeNi high entropy alloy (HEA) or complex concen

244 e main group center either at a single site (Al) or across a metal-metal bond (Mg-Mg).

245 will decompose and disappear, forming stable Al(2)O(3) and TiO(2) inclusions.

246 earth metals Tm and Lu partially substitute Al atoms in the structure of the Zintl phase Ca(14)AlBi(

247 The surface Al(2)O(3) layer, formed after an initial thermal oxidati

248 loped a ternary liraglutide/tannic acid (TA)/Al(3+) nanoparticle system based on hydrogen bond format

249 s to a planar bicyclic frame with a terminal Al-O(*-) radical site, accompanied by a change from the

250 (8)O(12)(+) which also features the terminal Al-O(*-) radical site.

251 , a new site created by a second tetrahedral Al atom and its hydroxyl group protons in zeolite HZSM-5

252 We demonstrate that Al(3+) induces a strong local distortion within the modi

253 Here we show that Al(3+) or Co(3+) are the ideal dopants and this is in ag

254 The Al atom in 2 is one-coordinate, and the compound display

255 The Al-based QSs fabricated using ultrashort pulsed laser ar

256 The Al-doping effect on the long/short range structural evol

257 The Al-N unit is highly polar, and capable of the activation

258 The Al-P concentration under NPK + S and OM treatments incre

259 The Al-QS were up taken by the cells through label-free self

260 he bond formation and bond activation at the Al sphere: thus, not only does it undergo electron redis

261 his second acidic proton site created by the Al(IV)-2 species are shown to be controlled via postsynt

262 ng of Crystal Violet and Rhodamine 6G by the Al-QS was driven up to single molecule sensing (femtomol

263 ), a cancer biomarker was also tested by the Al-QS.

264 distortions, resulting in an increase in the Al and/or Si coordination number.

265 an unusually broad composition range in the Al-Cu-Fe-Cr system.

266 Here, we investigate the Al(3+) intercalation chemistry of anatase TiO(2) and how

267 er of Mo and Y/Sc and Kagome ordering of the Al atoms, as evident from X-ray diffraction and electron

268 The replacement of the Al- by an Fe atom leads to a planar bicyclic frame with

269 Moreover, the imposed restriction on the Al nanoparticle location, i.e., only on the sample subst

270 ents of liquid steel tend to be uniform, the Al(2)O(3)-TiO(x) inclusions will decompose and disappear

271 resis (0.9 V) when compared to FETs with the Al layer (V(Dirac) = - 6.1 V and hysteresis = 2.9 V).

272 the formation of delta-Al(2) O(3) and theta-Al(2) O(3) .

273 tructure in the range where delta- and theta-Al(2) O(3) are formed represents a formidable challenge,

274 er in delta-Al(2) O(3) and twinning in theta-Al(2) O(3) and show that explicitly accounting for the d

275 of delta-Al(2) O(3) is stabilized with theta-Al(2) O(3) even after prolonged high-temperature exposur

276 XM(YCH(2)CH(2))(3)N (M = Si, Ge, Sn, Pb, Ti, Al, Cr, Fe, Ni...; Y = O, NR, CH(2), S), i.e., substitut

277 reasing the basicity and the ratio of CaO to Al(2)O(3) in the initial slag.

278 actions, primarily tannin-like compounds, to Al(2)O(3).

279 r 60 or 42 days of exposure, rats exposed to Al and EWH did not show memory or cognitive dysfunction

280 pect to C-H bond activation, very similar to Al(8)O(12)(+) which also features the terminal Al-O(*-)

281 ata indicates the behavior of 4 and P toward Al(3+) is pH independent in medium conditions.

282 The response of the chemosensor HMBP towards Al(3+) was attributed to the strategies of blocking the

283 of primary alpha-Al dendrites and ultrafine Al-Si eutectic of lamellar morphology.

284 urated oxygen in steel easily forms unstable Al(2)O(3)-TiO(x) inclusions with [Ti].

285 The ability of in vitro cell detection using Al-QS was analyzed with three cell lines, mammalian fibr

286 h temperature to eliminate oxygen vacancies, Al is doped into the ZnO nanosheet, and the memristive b

287 atalytic diversity among zeolites of varying Al arrangement.

288 Viable Al-ion batteries require suitable electrode materials th

289 etically viable reaction mechanisms by which Al-O and Si-O bonds rapidly and reversibly break at 300

290 ximately equal parts of Co and Ni along with Al, Cr, Ta and W that possess strengths in excess of 1.1

291 he binding constant of chemosensor HMBP with Al(3+) from the Benesi-Hildebrand equation was determine

292 XO(4)/XO(5)/XO(6) with X = {Al/Ga}) is established.

293 y) O(2) (NMC) and LiNi(1-) (x) (-) (y) Co(x) Al(y) O(2) (NCA) are the cathode materials of choice for

294 Herein, a high-Ni LiNi(1-) (x) (-) (y) Mn(x) Al(y) O(2) (NMA) cathode of desirable electrochemical pr

295 ynamically stable, atomically thick CuCr(1-x)Al(x)O(2) interfacial layer is the critical element for

296 abricated with a restively shunted Nb/AlO(x)-Al/Nb process that did not include MJJs.

297 the framework Al arrangement (Al-O(-Si-O)(x)-Al, x = 1-3) among CHA zeolites of essentially fixed com

298 erials with general formula of LiNi(x) Fe(y) Al(z) O(2) (x + y + z = 1), termed as the lithium iron a

299 z)Co(1-y-z)O(2) (NMC) and Li(x)Ni(y)Co(1-y-z)Al(z)O(2) (NCA) show reduced first cycle Coulombic effic

300 A Cu-Zn-Al/AAS hybrid shows excellent performance for CO(2) to f