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1 the binder is composed of an allophane-like clay.
2 an blue pigment was also mixed into the dyed clay.
3 s via the attachment of nanoparticles to the clay.
4 (>7.0) and generally contained >200 mg g(-1) clay.
5 y to examine relatively undiluted authigenic clay.
6 ld a three-dimensional representation of the clay.
7 s with biologically/chemically reduced model clays.
8 cid modification of Na-enriched and pillared clays.
9 es in what may be very rapidly deposited CIE clays.
10 r alone, with illite outperforming the other clays.
11 l) components on the surface compositions of clays.
12 present as exchangeable Fe oxyhydroxide and clay-adsorbed Se(4+), and 39% of Se is present as organo
14 rived from in situ weathering, and exogenous clay and silt, which entered the chamber through fractur
15 r many centuries in Xinjiang, as depicted in clay and wooden figurines unearthed in the Astana cemete
16 cess, utilizing porous catalysts composed of clay and zeolite, converts heavy crude-oil fractions int
17 inary wares; (ii) intervalley homogeneity of clays and fabrics for a wide range of decorated wares (e
18 sults show: (i) intervalley heterogeneity of clays and fabrics for ordinary wares; (ii) intervalley h
21 ent-free crystals and solids such as silica, clay, and zeolite and water-soluble hosts that can solub
29 he initial shape and dispersion state of the clay as well as the nanoparticle/clay concentration rati
33 olymer, carbonaceous, metal, metal oxide and clay) based modified electrodes for the sensing of NADH.
37 etreated by iron-sulfate-clay slurries (iron-clay biochar), as compared to untreated bamboo biochar.
39 to measure temporal gains/losses of surface clay caused by periodic wind erosion (dust) and rainfall
41 elite=3:4:1 and com II; bentonite: activated clay: celite=3:4:1+1% citric acid) on the physico-chemic
46 tate of the clay as well as the nanoparticle/clay concentration ratio also affected the nature of the
47 variation among mineral soils in soil C and clay concentrations, soil delta(15)N showed no consisten
48 of OC is also related to grain size with the clay containing mostly (immature) plant derived OC and s
49 creases for this reaction in the presence of clay-containing ATPS over clay in buffer alone, with ill
53 es with pre-existing phyllosilicate-bearing (clay content </=3 wt.%) micro-layers weaken faster than
54 ropose that, within calcite gouge, ultra-low clay content (</=3 wt.%) localized along micrometer-thic
55 L kg(-1), n=19), and was correlated with the clay content (relation to log10(Kr, linear), r2=0.40, n=
58 ctivation would be unlikely because the high clay content of caprocks ensures a reduced permeability
59 he soil properties; a high organic matter or clay content was observed to negatively affect the recov
62 organic C (POC, HOC, and ROC, respectively), clay content, cation exchange capacity (CEC), pH, volume
63 e BJH pore volume is positively related with clay content, suggesting N2GA is suitable for describing
64 soil organic carbon (C), soil C:N ratio, and clay content, where Q10 was primarily influenced by the
68 s, porous composites composed of zeolite and clay crack the heavy fractions in crude oil into transpo
71 to organic carbon and organic carbon-coated clays dominate U(IV) speciation in an organic-rich natur
72 linite; therefore, Ca(2+)-bridging of BPS to clay edge sites was assessed by comparing sorption from
74 correlated to the reduction potential of the clay (EH,clay, R2=0.95 for both minerals), indicating th
76 ir microporous nature nanosized zeolites and clays exhibit novel properties, different from those of
77 by added/sorbed Fe(II) (if Fe(II)SORBED > 8% clay Fe(II)LABILE); however, the kinetics of this concep
79 was caused by different forms of structural clay-Fe(II) in the clay minerals and different reduction
80 logical activity, the reactivity of biogenic clay-Fe(II) toward reducible contaminants is particularl
81 s are ubiquitous in the environment, and the clay-Fe(II)/Fe(III) redox couple plays important roles i
82 with NAu-2 and biogenic uraninite, 16.4% of clay-Fe(III) was reduced in the presence of excess urani
84 s of sauconite identifying new mechanisms of clay formation in surface environments of rocky planets.
85 esent experimental evidence that shows rapid clay formation under conditions that would have been pre
87 over the Cenozoic reduced marine authigenic clay formation, contributing to the rise in seawater Mg/
88 e and mudstone seals is heavily dependent on clay fraction and can be extremely low even in the prese
90 er component was found in the sand, silt, or clay fraction while the structural component was exclusi
91 roportion of microbial-derived C in the silt-clay fraction, as compared with that in adjacent soils t
92 ctionated into sand, silt, and (if possible) clay fractions as well as hand-picked calcine pebbles.
96 In the constrained interlayer regions of the clay, hydrated electrons and co-sorbed PFCs are brought
97 in the presence of clay-containing ATPS over clay in buffer alone, with illite outperforming the othe
100 clays in tailings ponds and the behaviors of clays in diverse industrial and natural environments.
101 anced applications of nanosized zeolites and clays in free (suspension and powder forms) and fixed (f
102 itative insights underlying the stability of clays in tailings ponds and the behaviors of clays in di
105 f solution of as-received and "contaminated" clays, in as-received and "contaminated" organic solvent
106 ely mediated by cation exchange in micaceous clays, in particular Illite-a non-swelling clay mineral
109 -indole-acetic-acid within an organomodified clay induce the reductive defluorination of co-sorbed PF
111 s loop is consistent with SEM observation on clay inter-crystalline pores while BJH pore volume is po
112 wn to dominate the energetics of the solvent-clay interaction, and organic liquids as solvents or as
115 Illite has been widely studied, because this clay is especially relevant for Cs migration-retention i
116 in the environment is greater where percent clay is less than 18% and soil pH is greater than 6.6.
117 evolution model; we find that the primordial clay is locally disrupted by impacts and buried by impac
118 We compared the three main types of natural clay: kaolinite, montmorillonite and illite, all of whic
119 d octahedral (structural) Fe(III) within the clay lattice, as well as between aqueous Fe(II) and stru
120 teristics of these nanocomposites, including clay-layer spacings, out-of-plane clay-sheet bending ene
121 ince been dedicated to the study of silicate clays, layered double hydroxides, believed to be common
122 y are discussed in this review with focus on clays, layered transition metal oxides, silicates, layer
123 sand into and subsequently out of kaolinite clay layers of vertical thickness 15 mm, 20 mm, and 60 m
125 method to construct a complex and realistic clay-like nanoparticle aggregate with interparticle pore
126 for a given soil especially for the two high clay low OC soils, BPS sorbed much more than expected re
130 sequestration by a lanthanum (La) exchanged clay mineral (La-Bentonite), which is extensively used i
132 reverse tricarboxylic acid (rTCA) cycle and clay mineral catalysts coevolved remains a mystery in th
133 increase in reduction potential results from clay mineral dissolution resulting in increased Fe(III)
134 iments motivated by the hypothesis that some clay mineral formation may have occurred under oxidized
135 arly Hesperian or younger age indicates that clay mineral formation on Mars extended beyond Noachian
136 Microdiffraction imaging identified the clay mineral kaolinite to play a key role in the immobil
138 Here we explore the distribution of natural clay mineral particles in poly(ethylene glycol) (PEG)/de
140 Adsorption and redox transformations on clay mineral surfaces are prevalent in surface environme
142 approach is applied to study collections of clay mineral tactoids interacting with two synthetic pol
143 s clays, in particular Illite-a non-swelling clay mineral that naturally contains interlayer K(+) and
144 Using experimental data on an iron-bearing clay mineral, we illustrate how mediated electrochemical
148 distinct microbial communities more so than clay mineralogy, where microbial-derived SOM accumulatio
151 on rate constants by bioreduced iron-bearing clay minerals (montmorillonite SWy-2 and nontronite NAu-
152 erent forms of structural clay-Fe(II) in the clay minerals and different reduction potentials (Eh) of
153 These results suggest the coevolution of clay minerals and early metabolites in our planet could
154 between aqueous Fe(II) and structural Fe in clay minerals and electron conduction in octahedral shee
155 cs of Cr(VI) reduction by Fe(II/III)-bearing clay minerals and may improve predictions of Cr(VI) beha
156 for further studies on the sorption of Tl to clay minerals and Mn-oxides and its impact on Tl solubil
158 tals can be associated with soil components (clay minerals and organic matter), biosolid application
159 the high capacity for binding of arsenic to clay minerals and oxides of iron and aluminum in subsoil
160 the fossils are composed of aluminosilicate clay minerals and some carbon, a composition comparable
164 idence that Fe(II) uptake characteristics on clay minerals are strongly correlated to the redox prope
166 ity toward reductive dissolution, Fe-bearing clay minerals are viewed as a renewable source of Fe red
171 r reaction controlling its mobilization, and clay minerals could mitigate As mobilization with surfac
172 pidly than biologically reduced iron-bearing clay minerals despite the minerals having similar struct
175 E distinguishes Fe(III) reduction of layered clay minerals from that of Fe oxyhydroxides, where accum
176 redox interactions between sorbed Fe(II) and clay minerals gained in this study is essential for futu
177 e of simple oxide surfaces: edge surfaces of clay minerals have a variable proton surface charge aris
179 Our finding of 5-20% Fe atom exchange in clay minerals indicates that we need to rethink how Fe m
182 ise the question whether Fe interaction with clay minerals is more dynamic than previously thought.
183 that: (1) As desorption/adsorption from/onto clay minerals is the major reaction controlling its mobi
184 electron donor, we found that the Fe-bearing clay minerals montmorillonite SWy-2 and nontronite NAu-2
185 We calculated that 5-20% of structural Fe in clay minerals NAu-1, NAu-2, and SWa-1 exchanged with aqu
187 demonstrated the rapid formation of Fe-rich clay minerals of variable crystallinity from aqueous Fe(
189 chemically reduced (dithionite) iron-bearing clay minerals reduced nitrobenzene more rapidly than bio
192 aining soluble reduced metals and expandable clay minerals that absorb cations, providing a capacity
193 ematic oscillations of various evaporite and clay minerals that can be linked to the variation of reg
194 study, the retention mechanism of Fe(II) on clay minerals was investigated using macroscopic sorptio
195 uction on soil surrogates composed of HA and clay minerals was studied by use of a coated-wall flow r
199 mentally relevant surfaces (Fe (hydr)oxides, clay minerals, and soil from Arizona and the Saharan Des
200 -toxic ionic aluminium (Al(3+)) species from clay minerals, driving the evolution of counteractive ad
202 (hydr)oxides were dominantly associated with clay minerals, suggesting that their dispersion as free
203 ffect on Cr(VI) reduction kinetics: for both clay minerals, the rate constant of Cr(VI) reduction var
204 many inter-crystalline pores are produced in clay minerals, this type of pores is not the most import
215 aqueous Cr(VI) with two abiotically reduced clay minerals: an Fe-poor montmorillonite and an Fe-rich
217 s of atmospheric CO2 on amine-functionalized clay nanotubes followed the fractional-order kinetic mod
220 we suggest that most of the magnetite in the clay occurs as isolated, near-equidimensional nanopartic
222 can explain the present distribution of many clays on Mars, and the anomalously low density of the Ma
223 avior in two different clay stones, Opalinus Clay (OPA) and Helvetic Marl (HM), was studied using a w
224 e oxidized forms of Pu(V,VI) within Opalinus Clay (OPA) rock, a heterogeneous, natural argillaceous r
226 candidates for the "active sites" that make clay particles effective nucleants for ice in the atmosp
228 chemical and physical properties of silt and clay particles that occlude organic matter from microbia
231 a finite Fe(III) pool along the edges of the clay particles, accompanied by a limited release to solu
237 -matrix composites--such as nacre, silk, and clay-polymer-exhibit a remarkable balance of strength, t
240 troscopy shows that the presence of the iron clay prevents degradation of the cellulosic fraction at
241 m chloride salt crystals and Montmorillonite clay, previously proposed to promote polymerization.
242 higher temperatures (350-550 degrees C), the clay promotes biomass degradation, resulting in an incre
244 lite with spectral bands designed to measure clays, quartz and other minerals were released in 2012 f
245 d to the reduction potential of the clay (EH,clay, R2=0.95 for both minerals), indicating that the cl
246 0.95 for both minerals), indicating that the clay reduction potential also influences its reactivity.
247 ning and oilsands production industries, and clay rehabilitation following contamination poses challe
248 water or hydroxyl groups in ancient martian clays retains the imprint of the water of formation of t
249 hermore, we explore the fate of a primordial clay-rich layer with the help of a parameterized crustal
250 are exclusively H. naledi, and occur within clay-rich sediments derived from in situ weathering, and
251 ndrite Khatyrka recovered from fine-grained, clay-rich sediments in the Koryak Mountains, Chukotka (R
252 ia magnetosome chains, have been reported in clay-rich sediments in the New Jersey Atlantic Coastal P
253 ding forms in aggregates taken from a high-P clay-rich soil and a low-P sandy soil by combining advan
254 igher fullerol mineralization in an organic, clay-rich soil versus a silty, low C soil ( approximatel
255 ment images of a cesium-infiltrated Opalinus clay rock were recorded using LA with a laser-spot diame
256 om heterogeneous materials, such as Opalinus clay rock, will remain a challenge for 3D LA-ICPMS imagi
257 major and minor constituents in an Opalinus clay-rock sample at a 1.5 mum laser-spot diameter and qu
259 including clay-layer spacings, out-of-plane clay-sheet bending energies, X-ray diffractograms, and m
260 ctericidal mechanism demonstrated by natural clays should guide designs of new mineral-based antibact
265 bamboo biomass is pretreated by iron-sulfate-clay slurries (iron-clay biochar), as compared to untrea
266 s: a sandy soil poor in organic matter and a clay soil rich in organic matter, both contaminated with
267 ganic matter (OM)-rich peat soil, an OM-poor clay soil, a hydrophilic Aldrich humic acid salt, and wa
271 by using a set of storage jar handles (fired clay) stamped by royal seals as part of the ancient admi
273 uivalent pores are small pores in compressed clay stones that are small enough to have, because of ov
274 he anion exclusion behavior in two different clay stones, Opalinus Clay (OPA) and Helvetic Marl (HM),
277 red interaction force between bacteria and a clay surface, and the approach curves exhibited jump-in
278 this transition, which is observed on model clay surfaces, mica, but not on silica surfaces nor for
281 Notably slower Fe(II) precipitation in the clay suspensions compared to gamma-Al2O3 and SiO2 is att
282 amical process of polymer intercalation into clay tactoids and the ensuing aggregation of polymer-ent
283 iscrimination of illite from montmorillonite clays that typically develop in large depositional envir
286 eactivity studies are based on reduced model clays, the reactivity of naturally reduced field samples
288 such as carbon-based 2D materials, silicate clays, transition metal dichalcogenides (TMDs), and tran
292 on semiconductor minerals, the synthesis of clays was demonstrated at low temperature and ambient pr
293 ever, that a substantial proportion of these clays was formed when Mars' primary crust reacted with a
294 th previous rock magnetic studies on the CIE clay, we suggest that most of the magnetite in the clay
296 Amazonian rain forest, including terra firme clay, white-sand and seasonally flooded forests in Peru
298 r all compounds across the various homoionic clays with sorption coefficients (Kd) decreasing as foll
301 hydrothermal fluids becomes concentrated in clays within caldera lake sediments to potentially econo
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