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1 and the selective nature of Tl(+) uptake by illite.
2 asured with CO(2) (273 K) in the presence of illite.
3 I) into Mn-oxides and the uptake of Tl(I) by illite.
4 ffect of the electrolyte on the structure of Illite.
5 and is likely part of clay minerals such as illite.
6 s study, we investigated Pu sorption onto Na-illite, a relevant component of potential host rocks for
7 n exchange in micaceous clays, in particular Illite-a non-swelling clay mineral that naturally contai
9 V) were detected in solution on contact with illite after 1 week, which is not expected to be stable
10 natural clay: kaolinite, montmorillonite and illite, all of which are aluminosilicates of similar com
13 l surfaces (montmorillonite for nucleotides, illite and hydroxylapatite for amino acids) induces the
14 t spectroscopic evidence for Tl(I) uptake by illite and indicates the need for further studies on the
16 0% of the cation-exchange capacity (CEC) for Illite and kaolinite and below 1 mmol/kg (<1% CEC) for b
17 roduced unexpected enhancement of Ti(+) from illite and kaolinite clays that contained small quantiti
18 stigated REE adsorption to the clay minerals illite and kaolinite through pH adsorption experiments a
19 5.0 m/day using columns packed with the same illite and quartz mass however with different spatial pa
21 a stacking of layers identical to endmember illite and smectite layers, implying discrete and indepe
22 sure of authigenic ferrimagnetic minerals by illite and vermiculite-group minerals inhibits their che
23 adsorption to quartz, goethite, birnessite, illite, and aquifer sediments induced an average isotopi
30 emonstrate the requirement of accounting for Illite decollapse especially for high Cs loadings, becau
34 (2+) from microbial reductive dissolution of illite/Fe-oxides may be exported to the water column.
36 yered illite-smectite indicating progressive illite formation, (2) electron microprobe mapping and ED
37 and its weathering products with diagenetic illite formed by reaction with pore fluids during burial
38 water content, enables the discrimination of illite from montmorillonite clays that typically develop
39 K-Ar dating of authigenic, syn-weathering illite from saprolitic remnants constrains original base
42 osilicates such as vermiculite, biotite, and illite, have demonstrated great potential in various fie
43 ), illite-smectite mixed layer (ISCz-1), and illite (IMt-2)-using CO(2) and CH(4) up to 30 MPa at 25-
44 III); 8 x 10(-11) < [Pu]tot/M < 10(-8)) with illite in 0.1 M NaCl at pH between 3 and 10, Pu uptake w
45 actions of Tl(III), Tl(I)-jarosite and Tl(I)-illite in bulk samples based on XAS indicated that Tl(I)
46 helf C has revealed microbial alterations of illite in marine sediments, a process typically thought
48 ography, for interpreting the K-Ar ages from illites in sedimentary rocks and for estimating the ages
49 omplexation constants determined for Eu(III)-illite interaction (with redox-insensitive Eu(III) as a
51 s study is to analyze how Cs adsorption onto Illite is affected by structural changes produced by the
54 Sorption to the phyllosilicate clay minerals Illite, kaolinite, and bentonite has been studied for a
58 minerals (ferrihydrite, goethite, kaolinite, illite, montmorillonite) using the CuO-oxidation techniq
61 he identification of kaolinite, chlorite and illite or muscovite, and a new class of hydrated silicat
63 Here, we show high K content confined to illite particles that are abundant in the facies bearing
65 Cs sorption isotherms were carried out with Illite previously exchanged with Na, K, or Ca, at a broa
67 ence for the microbially induced smectite-to-illite (S-I) reaction has previously been shown using cu
68 have been thought to control the smectite-to-illite (S-I) reaction, an important diagenetic process u
69 rom 10(-9) to 10(-2) M at near-neutral pH on illite saturated with Na(+) (100 mM), K(+) (1 and 10 mM)
70 aluation of the evolution of the smectite-to-illite sequence of clay minerals, including the nature o
71 and decreased expandability in mixed layered illite-smectite indicating progressive illite formation,
72 cs and structures of these two models for an illite-smectite interstratified clay mineral with a rati
74 ay minerals-Na-rich montmorillonite (SWy-2), illite-smectite mixed layer (ISCz-1), and illite (IMt-2)
75 re principally Fe-Mg illite, mixed layers of illite/smectite and chlorite, with minor kaolinite and s
76 work examines the largely unexplored role of illite spatial distribution patterns in dictating the so
79 uptake as well as 10 A-clay minerals (e.g., Illite) that compete with water and chloride for N(2)O(5
80 ering-related transformation of iron-bearing illite to vermiculite, generating aggregates of vermicul
81 e compensation associated with the kaolinite-illite transition during burial diagenesis and metamorph
85 based on XAS indicated that Tl(I) uptake by illite was the dominant retention mechanism in topsoil m
86 g adsorption of Tl(+) at the frayed edges of illite, with Tl selectivity coefficients between those r
87 d 3.0 m/day, well-connected low permeability illite zones oriented in the flow-parallel direction lea