ライフサイエンスコーパス: adsorption site

1 nces the population of the stronger specific adsorption site.

2 shift of Bi atoms involving a change of the adsorption site.

3 structure and are independent of the surface adsorption site.

4 second electron is localized at the superoxo adsorption site.

5 NiO is still limited by lacking favorable H adsorption sites.

6 de) nanoparticles provided a large number of adsorption sites.

7 ants corresponding to the different types of adsorption sites.

8 vealed a total of eight symmetry-independent adsorption sites.

9 -sphere complexation mechanisms depending on adsorption sites.

10 evealed the presence and nature of different adsorption sites.

11 s at nanoscales on identifiable and distinct adsorption sites.

12 and C-F functionalizations serving as strong adsorption sites.

13 ty of nitrogen oxides and create more active adsorption sites.

14 a mathematical model involving two different adsorption sites.

15 tter suited to compete for aromatic-compound-adsorption sites.

16 they adsorb to a different subpopulation of adsorption sites.

17 ike tbo-MOF series with intrinsic strong CH4 adsorption sites.

18 by chemical blocking of nonselective surface adsorption sites.

19 different polymorphs and different types of adsorption sites.

20 o determine the most energetically favorable adsorption sites.

21 er specific surface area and abundant active adsorption sites.

22 d 5% for the saturation capacity of the weak adsorption sites.

23 adsorption on Na-Rho at 298 K identifies the adsorption sites.

24 dding constituents to compete with dsRNA for adsorption sites.

25 eferentially interacts with multiple surface adsorption sites.

26 h products to determine the number of strong adsorption sites.

27 mentally determined limited accessibility of adsorption sites (78%) is taken into account.

28 dicate that these result from changes in the adsorption site and bond formation between CO and O with

29 p hybridization) that facilitates changes in adsorption site and eventually leads to S-S bonding.

30 termolecular hydrogen bonds, and changes the adsorption site and footprint.

31 9% for the saturation capacity of the strong adsorption sites and 24% for the equilibrium constant an

32 ly delivering accurate information regarding adsorption sites and adsorption geometries of adsorbates

33 two prototypal model catalyst surfaces, the adsorption sites and configurations for hydrogen (H2), a

34 sual behavior are explained by analyzing the adsorption sites and diffusion mechanism for each specie

35 plications include precise identification of adsorption sites and establishment of rigorous molecular

36 It was achieved by resolving the identity of adsorption sites and geometries of (bi)carbonate species

37 i(0) nanoparticles to provide restored CH(4) adsorption sites and near-surface/dissolved C atoms, whi

38 distributions functions (pdfs) that describe adsorption sites and quantify uncertainty.

39 f charges are necessary to create detectable adsorption sites and that even chemically identical liga

40 AS) reveals that the cations do not block CO adsorption sites and that the cation-dependent interfaci

41 de energy relaxation is also affected by the adsorption sites and the nature of the metal but to a le

42 cause water competes with CO(2) for the same adsorption sites and thereby causes the materials to los

43 on region, which can be used to avoid strong adsorption sites and thus minimize their contribution to

44 an effectively identify the chemical nature, adsorption sites, and adsorption geometries of sulfur-ba

45 er, the relative populations of the specific adsorption sites are 11% and 17%, showing that acetonitr

46 ate constants for a cationic dye from strong adsorption sites are compared for the same chromatograph

47 surface strain) and optimizing the reactant adsorption sites are discussed and categorized based on

48 ity and, more importantly, the uniformity of adsorption sites are found as well to dictate the step p

49 , different lead orientations, and different adsorption sites are fully considered.

50 nounced for H(2) than D(2), and two distinct adsorption sites are identified with a subtle but signif

51 m large data sets, revealing that the strong adsorption sites are randomly distributed throughout the

52 the populations of DiI at these two specific adsorption sites are shown to be 11% and 4%, respectivel

53 The strong adsorption sites are smaller in size than the optical re

54 The sizes of strong adsorption sites are within the optical resolution of co

55 This data unequivocally shows that primary adsorption sites around, and within, the small octahedra

56 therms which suggest a diversity of graphite adsorption sites as confirmed by the presence of carboxy

57 Chromolith material had half as many strong adsorption sites as the Symmetry material.

58 diffusing and that there is a rare specific adsorption site associated with a 0.07-s desorption time

59 distinguish Lewis (L) and Bronsted-Lowry (B) adsorption sites at the GO surfaces.

60 tivity suggest surface saturation or reduced adsorption site availability.

61 tion and that there is a competition for the adsorption sites between anthocyanins and tannins that i

62 process is driven by the creation of stable adsorption sites between the carboxylate ligands, to all

63 ; specifically, the clustering of slow, rare adsorption sites broadens the peak, and this effect rema

64 rous nylon-6,6 films increased the number of adsorption sites but decreased the binding affinity comp

65 at the edge of the nanoparticle tunes local adsorption sites by affecting the d-orbitals of nickel.

66 nanostructures and that CO transports to Pt adsorption sites by an activated surface diffusion proce

67 thdrawing adsorbate, we show that reversible adsorption sites can be created on the nanotube array vi

68 In MeCN, three types of adsorption sites coexist for the two enantiomers on the

69 mechanical model relating volumetric strain, adsorption site concentration, and sorbed water concentr

70 Using SERS mapping, we visualize adsorption sites, confirming the nanopores' role as acti

71 ed the research community in identifying the adsorption sites, defect sites, structural or spin trans

72 to neo-formed minerals and that an increased adsorption site density coincides with the finer-grained

73 ing finding-that adsorption increases as the adsorption site density decreases-is associated with imp

74 ated for the first time by creating a higher adsorption site density with a polymer amine, such as po

75 nsity calculations further indicate that the adsorption site, distance, and molecular polarization of

76 We find a modified adsorption site distribution and higher diffusivities fo

77 a manner that defies the classical picture: adsorption sites either do or do not share electrons ove

78 engender a basic error: predicting the wrong adsorption site for CO (a key CO(2)RR intermediate) on t

79 suggest metallic cobalt as the preferential adsorption site for CO(2) compared to hardly reducible c

80 ir crystal structures we propose a molecular adsorption site for nitrobenzaldehyde.

81 e quercetin UV-visible spectra show that the adsorption site for pyrene and quercetin in bile salt mi

82 pmost Pd surface atoms provide the preferred adsorption sites for all studied molecules.

83 The primary adsorption sites for Ar and N2 within metal-organic fram

84 igher coverage, steps are the most favorable adsorption sites for atomic H adsorption, and it is like

85 ation energy (-3.99 kJ mol(-1)) and specific adsorption sites for Cd-MOF-LF.

86 in predicting the stability of the different adsorption sites for CO on transition metal surfaces.

87 suggest that metal sites provide preferable adsorption sites for fluorocarbon based on favorable C-F

88 ar -OH groups, both of which serve as strong adsorption sites for polarizable Xe gas.

89 ts its open-pore structure, providing unique adsorption sites for selective CO(2) adsorption and pack

90 atic energy shuttles that act as noncovalent adsorption sites for substrates on the QD surface, the s

91 experiments have given some insight into the adsorption sites for the chiral molecules on the Cu(643)

92 teractions associated with the preferen-tial adsorption sites for the organometallic precursors prior

93 diffraction studies on NOTT-101 reveal three adsorption sites for this material: at the exposed Cu(II

94 concentration of accessible hydrogen-bonding adsorption sites for water.

95 als the presence of a third type of specific adsorption site, for which DiI has a desorption time in

96 gth between the adsorbent and adsorbate, and adsorption site heterogeneity.

97 involve surface-induced nucleation, with ion adsorption sites (i.e., functional groups) serving as an

98 Interestingly, the strongest adsorption sites identified are associated with the arom

99 demonstrate that the spatial distribution of adsorption sites impacts peak broadening; specifically,

100 e significantly higher than those on typical adsorption sites in classical MOFs, consistent with the

101 tions to co-adsorbing at the most favourable adsorption sites in gas separation and storage applicati

102 ction study reveal the position of the water adsorption sites in MOF-801 and highlight the importance

103 gen and nitrogen occupy distinctly different adsorption sites in the pores, with very different limit

104 ween the two solids types or competition for adsorption sites in the presence of silicate.

105 CO2 reveal the presence of several distinct adsorption sites in the solid, which are attributed to t

106 open Cu(II) sites are the secondary/tertiary adsorption sites in these structures.

107 ayer are preferentially adsorbed at specific adsorption sites, involved in about 20% fewer hydrogen b

108 orrelation methods for finite-size models of adsorption sites is employed to calculate energies for a

109 t the interactions between gas molecules and adsorption sites is essential to customize metal-organic

110 e site on this catalyst, and a separation of adsorption sites is proposed as the cause of this inhibi

111 , and conductance all depend strongly on the adsorption site, lead orientation, and local contact ato

112 anchoring atom increases, regardless of the adsorption site, lead orientation, or bias.

113 tronger adsorption at the higher coordinated adsorption site leads to a more stable catalyst.

114 monstrate by a simple model that counterions adsorption sites located on the inner face of the NT wal

115 Hence, water can out-compete CO(2) for adsorption sites, lowering the working CO(2) sorption ca

116 competent gas storage materials and further adsorption sites may be optimized by judicious ligand fu

117 and revealed the presence of very strong CH4 adsorption sites near the organic linker with similar ad

118 by the different gases, starting with strong adsorption sites near the Zr atoms, a result corroborate

119 Changes in coverage and adsorption site of CO were followed by XPS and SFG up to

120 ed STEM-EDX data revealed that the preferred adsorption sites of both As(III) and As(V) are at GR cry

121 ce correlation imaging are used to study the adsorption sites of C(18) silica beads under RPLC chroma

122 d both FeO6 and MnO6 octahedra; however, the adsorption sites of Fe(III) hydrous oxides played a lead

123 The contribution of the adsorption sites of Mn(III) oxide increased as the pH de

124 nner-sphere complexation (via oxygen) to the adsorption sites of the amorphous Fe(III) and Mn(III) ox

125 hat even chemically identical ligands create adsorption sites of varying kinetic properties that depe

126 states of a single molecule by changing its adsorption site on NaCl.

127 oc-L-Trp(OPfp) find three different types of adsorption sites on both the MIP and the NIP.

128 This suggests that P actively competes for adsorption sites on Fe nanoparticles, displacing adsorbe

129 perimental error, suggesting that the strong adsorption sites on fused silica are chemically the same

130 TC adsorption because of the competition of adsorption sites on KMBC.

131 ual presence of a low density of high-energy adsorption sites on Resolve-C18 were validated by measur

132 The presence of a few high-energy adsorption sites on Resolve-C18, with an adsorption ener

133 These LMWOAs compete with P for adsorption sites on soil minerals and induce dissolution

134 between H(4)SiO(4)(0) and H(3)AsO(3)(0) for adsorption sites on soil solids and subsequent plant-upt

135 nd under-coordinated (e.g., edge, vertex) CO adsorption sites on the 2 nm Pt nanoparticles as measure

136 The specific adsorption sites on the exsolved Rh particles lead to st

137 ow and high loadings, two additional methane adsorption sites on the exterior surface of the cage are

138 s were made to estimate the concentration of adsorption sites on the GO surface.

139 mptotic limit corresponding to the number of adsorption sites on the molecule.

140 ucing intermediates and the blocking of O(2) adsorption sites on the nanoparticle surface.

141 sorption is followed by the filling of other adsorption sites on the nodes and organic framework.

142 o 0.6 kcal/mol as corresponding to localized adsorption sites on the organic and inorganic components

143 free ion diffusion pathway and highly active adsorption sites, on carbon felt electrodes (CoNiPS@CF)

144 CO2 at 2 kbar reveals the presence of three adsorption sites, one previously unreported, and resolve

145 quire at least two adjacent and empty atomic adsorption sites (or vacancies).

146 e of the cage are apparent for a total of 56 adsorption sites per cage.

147 ional spectra aid in identifying species and adsorption sites present in experimental studies.

148 ted CO(2) reduction by competing for surface adsorption sites, preventing the potential-dependent str

149 SERS spectra but also their orientation and adsorption site, providing a detailed atomistic picture

150 n adherency on algal exudates, and triclosan adsorption site reduction on algae surface owing to P25'

151 sive swelling behaviour of APIP exposes more adsorption sites, resulting in a high Li(+) extraction c

152 can be attributed to the highly hydrophobic adsorption sites sandwiched by two pyrene linkers and th

153 and SAW do not directly compete for surface adsorption sites, SAW suppresses H*.

154 This approach to identifying and quantifying adsorption sites should be useful for designing better c

155 adsorbent material for gas pollutants, with adsorption site specificity taken into account.

156 separations usually consist of channels with adsorption sites spread relatively uniformly across the

157 tion isotherm parameters (number of types of adsorption sites, surface concentration of each type of

158 n these groups and the corresponding surface adsorption sites (Tb(3+) sites in our case).

159 both materials were used to locate four CD4 adsorption sites that fill sequentially.

160 walls rather than with the normally stronger adsorption sites (the open metal sites) within the frame

161 Although surface TiOH groups are the likely adsorption sites, the data show removing hydroxyl groups

162 ht into the thermodynamics of the individual adsorption sites, the tuning of which is paramount for o

163 es the adsorption mechanism and preferential adsorption sites to be resolved.

164 sing the scaling relations between different adsorption sites to break.

165 we physically limit the available molecular adsorption sites to only the electromagnetic "hot spots"

166 ultiple molecules link the stronger specific adsorption sites to specific locations on the surface.

167 monolayer capacity of the nonchiral type of adsorption sites was 22.9 mM.

168 rotein adsorption with slow kinetics and few adsorption sites was established as a source of peak bro

169 By imaging more than 70,000 single adatom adsorption sites, we compare the site preference and dyn

170 r simulations reveal four classes of surface adsorption site, where the prevalence of these sites dep

171 e and can explore the most favorable surface adsorption sites, whereas D2 is essentially immobile.

172 cules render higher concentrations of vacant adsorption sites which can accommodate an additional lay

173 m the dominating axial ligand field at the O adsorption site, which leads to out-of-plane uniaxial an

174 l that C(60) possesses multiple strong metal adsorption sites, which favors stable and uniform deposi

175 at combining Ni and Cu produces a variety of adsorption sites, which possess near-optimal hydrogen bi

176 n support (Zn(1)/NOC) serve as dedicated *OH-adsorption sites, while Ir-modulated Pt(100) nanocubes s

177 The existence of adsorption sites with a very high energy for certain com

178 Adsorption sites with abundant electron density on edges

179 -molecule observations revealed rare, strong adsorption sites with activity that varied significantly

180 ar windows of the cage are favorable methane adsorption sites with CD(4)-arene interactions between 3

181 he orbitalwise nature of chemical bonding at adsorption sites with d-states characteristics ranging f

182 n trapping due to the formation of selective adsorption sites with specific affinity for the differen

183 n microcalorimetry, we show that once strong adsorption sites within nanoscale network are taken, gas

184 ction (scXRD) study that identifies discrete adsorption sites within Ni-MOF-74/Ni-CPO-27, where SO(2)

185 ed to the Langmuir model, indicating uniform adsorption sites without significant interactions betwee