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 structure and are independent of the surface adsorption site.

3 second electron is localized at the superoxo adsorption site.

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

5 by chemical blocking of nonselective surface adsorption sites.

6 different polymorphs and different types of adsorption sites.

7 o determine the most energetically favorable adsorption sites.

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

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

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

11 eferentially interacts with multiple surface adsorption sites.

12 they adsorb to a different subpopulation of adsorption sites.

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

14 ants corresponding to the different types of adsorption sites.

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

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

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

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

19 9% for the saturation capacity of the strong adsorption sites and 24% for the equilibrium constant an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

104 Adsorption sites with abundant electron density on edges

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

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