Intercalation of naphthalene and anthracene into alkyltrimethylammonium (CnH2n+1(CH3)3N+; n = 8, 12, 14, 16, and 18)-montmorillonites was carried out by novel solid-solid reactions at room temperature. Octyltrimethylammonium(C8)-montmorillonite did not form an intercalation compound with either naphthalene or anthracene. Naphthalene was intercalated into both dodecyltrimethylammonium(C12)- and octadecyltrimethylammonium(C18)-montmorillonites to give intercalation compounds. On the other hand, the solid-solid reaction between dodecyltrimethylammonium(C12)- or tetradecyltrimethylammonium(C14)-montmorillonite and anthracene gave only partly intercalated compounds while hexadecyltrimethylammonium(C16)- and octadecyltrimethylammonium(C18)-montmorillonites gave single phase intercalation compounds. The hydrophobic interactions between alkylammonium-montmorillonites and the aromatic compounds are thought to be the driving force for the solid-state intercalation. The extent of the increase in the basal spacing may also be involved in the different reactivity.

The dissolution of two Ca2+-exchanged nontronite samples has been studied in 10% HCl. Early acid-dissolution studies (Osthaus, 1954) have indicated that after two hours of dissolution most of the octahedral Fe3+ (VIFe3+) would be removed leaving mainly tetrahedral Fe3+ (IVFe3+) in the nontronite structure. In the present study, 57Fe Mössbauer spectra of acid-treated samples were recorded and fitted with two octahedral Fe3+ (2 × VIFe3+) and two octahedral and one tetrahedral (2 × VIFe3+, 1 × IVFe3+) doublet models. The Mössbauer spectra of acid-treated Garfield nontronite samples could be adequately fitted with two-doublet models but acid-treated Hohen Hagen nontronite samples could not. Isomer shift and quadrupole splitting values obtained from the two-doublet models corresponded to VIFe3+ and not IVFe3+, as was suggested by the Osthaus (1954) experiment. When an IVFe3+ doublet was included in the model used to fit the Mössbauer spectra of acid-treated Garfield nontronite samples, a slight increase in the intensity of the IVFe3+ doublet occurred with increasing dissolution, but this was much lower than indicated by Osthaus (1954). No trend in the intensity of the IVFe3+ doublet was observed for acid-treated Hohen Hagen nontronite. Therefore, acid treatment appears to remove VIFe3+ and IVFe3+ from the nontronite structure at about the same rate. Mössbauer spectroscopy, infrared spectroscopy and X-ray powder diffraction data indicate that the nontronite that remains undissolved following acid treatment is structurally similar to the untreated nontronite.

Kaolinite:NaCl intercalates with basal layer dimensions of 0.95 and 1.25 nm have been prepared by direct reaction of saturated aqueous NaCl solution with well-crystallized source clay KGa-1. The intercalates and their thermal decomposition products have been studied by XRD, solid-state 23Na, 27Al, and 29Si MAS NMR, and FTIR. Intercalate yield is enhanced by dry grinding of kaolinite with NaCl prior to intercalation. The layered structure survives dehydroxylation of the kaolinite at 500°–600°C and persists to above 800°C with a resultant tetrahedral aluminosilicate framework. Excess NaCl can be readily removed by rinsing with water, producing an XRD “amorphous” material. Upon heating at 900°C this material converts to a well-crystallized framework aluminosilicate closely related to low-carnegieite, NaAlSiO4, some 350°C below its stability field. Reaction mechanisms are discussed and structural models proposed for each of these novel materials.

The crystal structure of bannisterite, a modulated, mica-like mineral species, of general composition Ca0.5(K,Na)0.5(Mn,Fe,Mg,Zn)10(Si,Al)16O38(OH)8·nH2O, has been solved and refined for specimens from Franklin Furnace, New Jersey (FF), and Broken Hill, Australia (BH). The crystals are mono-clinic in space group A2/a, with (for FF) a = 22.265(1) Å, b = 16.368(1) Å, c = 24.668(2) Å, β = 94.285(5)°; and (for BH) a = 22.286(1) Å, b = 16.386(1) Å, c = 24.575(2) Å, β = 94.355(7)°; Z = 8. Refinement with anisotropic thermal factors reached Rw = 0.034 (FF) and 0.039 (BH). Like stilpnomelane and ganophyllite, bannisterite has a modified 2:1 trioctahedral layer structure in which some of the tetrahedra are inverted towards the interlayer region and linked to inverted tetrahedra in the opposite layer. The octahedral sheet is strongly corrugated along b. The tetrahedral sheet consists of 5-, 6-, and 7-fold rings, and bond distance calculations indicate that Al is concentrated into two of the four inverted tetrahedra. The interlayer Ca, K, and H2O species are highly disordered, as indicated by anomalously large temperature factors and partial occupancies. Localized differences in the Al/Si arrangements in the inverted tetrahedra induce disorder among the interlayer cations.

Electrophoretic mobility of imogolite has been reported as positive (migration toward the negative electrode) below pH 9, and zero above pH 9. However, when mobility of dilute imogolite suspensions (5 × 10−3 kg/m3) was measured, it was found to be negative above pH 9. The reason that imogolite does not behave as a negative colloid when the clay concentration is not very dilute is because the imogolite forms floccules large enough to prevent migration. Imogolite has a PZNC at about pH 6, and has a PZC at pH 8.5–9.0 showing a relatively low absolute mobility under alkaline conditions compared to that under acid conditions. The fact that imogolite behaves like this is understandable given the location of negative charge appearing on the inside surface of the thin fibrous tube, according to the structural model of imogolite.

We report the first application of 39K solid-state NMR to the study of tecto- and phyllosilicates. Under high field (11.7 Tesla) and with the application of a spin-echo sequence, informative 39K spectra can be obtained for several compounds of interest to the geologist and the agronomist. Tectosilicates and phyllosilicates can be distinguished from the uncorrected frequency (δCG) of the observed NMR peak. A series of montmorillonites submitted to increasing numbers of wetting and drying cycles was studied in order to discriminate between mobile and “fixed” forms of K+: when the spectra are run on hydrated samples, two different signals are observed corresponding to K+ in different hydration states, and NMR data can be correlated with the amount of exchangeable K+ measured by ion exchange. Thus, it appears that NMR can provide useful information on K fixation complementary to classical chemical methods.

Decomposition of complex X-ray diffraction profiles is used on well characterized (image analysis of transmission electron micrographs, X-ray fluorescence chemical analyses) diagenetic samples from the Paris basin. The simultaneous occurrence of three “illitic” phases (mixed-layer illite/smectite or I/S, poorly crystallized illite, and mica-like phase) is shown on the various diffraction peaks of the 2–50 °2θ CuKα (44–1.8 Å) range. However, because of theoretical and experimental constraints, it is easier to perform the decomposition routine in the 5–11 °2θ CuKα (17.6–8.0 Å) range. The identification (i.e., illite content and mean coherent scattering domain size) of the various phases is performed by comparing the associated elementary peak characteristics (position, full width at half maximum intensity) with simulated X-ray patterns. When available, the characteristics obtained from the various angular regions are mutually consistent; however, the precise structures of smectite and illite end-members, on the one hand, and the structure of I/S crystallites, on the other hand, are not well known. Consequently, on some angular regions, there is a discrepancy between the characteristics obtained on experimental and calculated X-ray profiles. The definition of more realistic simulation hypotheses for I/S minerals, and for other interstratified clay minerals, would make this powerful and reliable tool to describe X-ray patterns a precise and sensitive identification tool even for complex clay parageneses.

In this paper, we use the unequal radius modified Gouy-Chapman theory to evaluate the effect of the ionic size of the electrolyte on the swelling pressures (II) in different clay systems immersed in electrolytic solutions. First the model is applied to a 1:1 electrolyte to show that the coion size is only important at surface charge densities much lower than those found in typical clay systems. The swelling pressure is calculated and the results are compared with experimental data. Literature ionic radii values are used to show the dependence of the swelling pressure on the specific counterions present. Next the model is applied to a 1:1 and 2:1 electrolyte mixture with unequal-sized counterions to show the swelling pressure is highly dependent on both counterion sizes. The unequal and same-sized cases are compared.

The long-term impermeability of clay barriers in waste disposal facilities and hydraulic structures is of critical importance to environmental, agricultural, and industrial concerns. Changes in the oxidation state of Fe in the constituent clays of compacted clay barriers may degrade the hydraulic conductivity of these structures because other properties related to hydraulic conductivity, such as swelling, gel microstructure, and particle size, are greatly altered by the oxidation state. Two Na-saturated smectites (SWa-1 and API 25) were reduced by sodium dithionite (Na2S2O4), both in suspension and in situ after consolidation, to examine the effects of structural Fe reduction on hydraulic conductivity. Results indicated that the hydraulic conductivity depended on both the oxidation state and the consolidation history of the clay. The hydraulic conductivity of clay reduced in suspension before consolidation was lower than that of oxidized clay. Initially reduced smectite, thus, may be compactable to a less-permeable material with higher bulk density. But reduction of smectite in situ after consolidation increased the hydraulic conductivity and its variability. The oxidized state of clay liners should, therefore, be preserved.

Hydrotalcites of high aluminum content have been synthesized from aluminate liquors of varying composition and activated magnesia obtained by calcination of hydroxide or hydroxycarbonate precursors. Lattice parameter measurements and chemical analyses of 21 synthetic hydrotalcites show that the aluminum substitution $$\left( {\rm{X = \frac{{Al}}{{Al + Mg}}}} \right)$$ for most of the products is about 0.35, which is at the maximum experimentally-observed limit of solid solubility. Pillared hydrotalcites were also prepared by molybdate, Chromate, and silicate anion replacement. A maximum distance of 10.4 Å between the brucite-like layers was observed for the Mo7O246− intercalated material.

Terra rossa samples were taken from the B horizons of soil profiles and from cracks within limestone in Italy. The average annual temperature (AAT) of the sites ranged from 8.4 to 20.3°C and the average annual precipitation (AAP) from 511 to 3113 mm, with either a 5–6 month water deficit or a large water surplus. Goethite and hematite were identified in all the samples. Under a moist (> 1700 mm AAP) and cool (13°C AAT) climate, a xeric, hematitic pedoenvironment was preserved by the well-litified carbonate rock. Hematite occurred in trace amounts, even with an AAT of 8.4°C and an AAP of 3300 mm, confirming the specific role of the hard limestone on the pedoclimate of terra rossa. The lowest mean crystallite dimension of goethite and hematite was found in the samples from the wettest sites, and in these samples hematite was nearly free of Al substitution. Rubification in terra rossa appeared to be due to the specific pedoenvironment. The hematite cannot be considered a relict phase formed under another climate. Illite and kaolinite were the main clay minerals in samples from xeric sites whereas more weathered clays, such as Al-interlayered vermiculite, occurred in cool, moist sites. We postulate that the processes of rubification and vermiculitization could have taken place at the same time.

X-ray diffraction studies of the pore-lining chloritic mineral from the Tuscaloosa Formation disclose a marked pattern of odd-order line broadening for the 001 to the 00,16 reflections. The odd-order peaks are approximately twice as broad as the even orders after correction for instrumental broadening effects. These results are consistent with a randomly interstratified 7-Å/14-Å structure, which is most likely serpentine/chlorite. Quantitative analysis of line broadening and model calculations indicate that the serpentine/chlorite contains 7% serpentine layers.

A simplified method is proposed for quantifying randomly interstratified serpentine/chlorite. Residual line broadening (βr) is obtained from the half-height widths of uncorrected diffraction profiles for the 004 and 005 “chlorite” reflections by means of the following:

${\beta }_r=({\beta }_{005}^{1.25}-{\beta }_{004}^{1.25}{)}^{\frac{1}{1.25}}.$

$\mathrm{\%}S=-0.51+24.27{\beta }_r,$

X-ray diffraction patterns were obtained from rock fragments, < 1 μm randomly oriented freeze-dried powders, and < 1 μm oriented aggregates for 11 mixed-layered illite/smectite samples (K-bentonites) that cover the range from 14 to 100 percent expandable. In all cases, 00l and hkl comparisons show no evidence of laboratory induced artifacts. Either the laboratory procedures caused no disaggregation of fundamental illite particles, or, if they did, fundamental particle reaggregation during sample preparation duplicated the one and three-dimensional structures of the illite/smectite in the original, untreated rock.

Demodulation of the 20l, 13l reflections into a two-dimensional band shape occurred with increasing percent expandable layers in illite/smectite. This result strongly supports the contention that turbostratic displacements occur at the expandable interfaces between fundamental particles, and are limited to those sites.

A comparison of the quantities measured by powder X-ray diffraction and high resolution transmission electron microscope (TEM) lattice fringe image techniques for disordered crystals suggests that meaningful comparisons between the two methods can be made only if a sufficient number of images are recorded to define the statistical parameters of the disorder.

Although phosphate sorption by goethite and other less-abundant Fe oxides strongly influences the concentration of this anion in the soil solution and aquatic environments, relatively little is known on the P-sorption characteristics of natural goethites. For this reason, we examined the P-sorption capacity and time course of P sorption of 10 goethite-rich soil, ferricrete and lake ore samples, in which the content and nature of mineral impurities were unlikely to affect P sorption significantly. Phosphate sorption could be adequately described by a modified Freundlich equation including a time term. The amount of P sorbed after 1 day of equilibration at a concentration of 1 mg P/liter ranged widely (0.36–2.04 /μmol P/m2). The total P sorbed after 75 days of equilibration varied less, in relative terms (1.62–3.18 μmol P/m2), i.e., a higher slow sorption tended to compensate for a lower initial (fast) sorption. Total sorbed P (X̄ = 2.62, SD = 0.52 μmol P/m2) was similar to the sorption capacity of synthetic goethites, suggesting a common sorption mechanism and the predominance of one type of crystal face, which, according to previous transmission electron microscope observations, might be the (110).

The extent of the slow reaction correlated to the ratio between micropore surface area and total surface area, as well as to oxalate-extractable Fe, which is an estimation of the ferrihydrite content. Ferrihydrite impurities might affect the slow reaction by contributing to the microporosity of some samples. Silicate adsorbed on the surface of the goethites was readily desorbed during phosphate sorption and did not significantly affect the extent of the slow sorption process.

The clay-polysaccharide interaction is of practical importance in the formation and stabilization of soil aggregates. This study examined the adsorption of three synthetic polysaccharides (PSS) and one soil PSS on Silver Hill illite. The adsorption of PSS was influenced by both the adsorbed cations on the adsorbents and the charge characteristics of the polymers. The adsorbed cations formed different surface complexes with the clay surfaces, with varying ability to screen the surface negative charge and thereby influenced the adsorption of charged polymers. Na-illite adsorbed substantially higher amounts of the cationic PSS, but lower amounts of the anionic PSS, than hydroxy-Al illite. The adsorption of the nonionic PSS was, however, little influenced by those adsorbed cations. The adsorption of the soil PSS resembled that of anionic PSS. However, it yielded linear adsorption isotherms due to the heterogeneous nature of the soil PSS. The adsorption of the three synthetic PSS on Na-illite was in the general order: cationic > nonionic > anionic, confirming that electrostatic forces played a role in the adsorption of charged polymers. pH and ionic strength influenced the adsorption of the charged PSS, because of their influences on the charge characteristics of both the polymer and the clay, and on polymer conformation. This study indicates that surface charge properties of both clays and organic polymers and the presence of polyvalent cations in the system are important factors influencing the complexation between soil clays and organic constituents.

57Fe Mössbauer spectra of two synthetic samples of ferrihydrite, recorded at 4.2 K in applied fields of up to 9 T, have been analysed by a mean-field model. The samples exhibit two and six X-ray diffraction peaks. It is shown that only one ferric ion site is present in the mineral, and that in this site the ions are octahedrally coordinated. The spectra show the presence of different magnetic states: ferrimagnetism in two-line ferrihydrite, and antiferromagnetism in six-line ferrihydrite. The ferrimagnetism in two-line ferrihydrite is analysed in terms of random fluctuations arising from the small numbers of ferric ions per particle, and it is shown that the different magnetic states may arise purely as a result of these fluctuations.

Transmission electron microscopy (TEM) was utilized to determine the origins of berthierine and chlorite in the core of the footwall alteration zone of the Kidd Creek massive sulfide deposit, Ontario. TEM images show lamellar intergrowths of packets of berthierine, mixed-layer chlorite/berthierine, Fe-Mg chlorite, and relatively Fe-rich chlorite that contain dislocations, stacking faults, kink bands, and gliding along (001). Interstratification of packets of berthierine and chlorite with one to several tens of layers commonly is associated with terminations of a layer of chlorite by two layers of berthierine. Layers in adjacent domains of berthierine and chlorite are continuous across interfaces that transect their common {001} planes. High-strain zones that cut across cleavage planes, consisting of distorted layers and lens-shaped pores, are associated with stacking faults and gliding along cleavage planes in chlorite crystals. Similar features separate interstratified chlorite/berthierine of different structures and textures, implying development of such composite grains after deformation of chlorite. Electron diffraction patterns show that the chlorite is an ordered one- or two-layer polytype or a one-layer polytype with semi-random stacking, and that the berthierine is a one-layer polytype with semi-random stacking epitaxially intergrown with chlorite.

Coexisting chlorite and berthierine have nearly identical ranges of compositions, containing Si ≅ 5, Al ≅ 6, and Fe ≅ 6.5–8.5 pfu, and minor, variable Mg and Mn contents, in formulae normalized on the basis of 20 total cations. This implies polymorphism among Fe,Al-rich members of the serpentine and chlorite groups. In one of the samples, berthierine and mixed-layer chlorite/berthierine coexist with chlorite having two compositional ranges, including Fe-rich chlorite with a relatively wide range of Fe-Mg contents, and a dominant Fe-Mg chlorite. In another sample, compositionally homogeneous Fe-rich chlorite is associated with berthierine and mixed-layer chlorite/berthierine; Fe-Mg chlorite was not detected.

The microstructural relations and the presence of coexisting polymorphs, complex mixed layering, heterogeneous polytypism, and wide ranges of mineral compositions are consistent with replacement of chlorite by berthierine under non-equilibrium retrograde conditions, in contrast to the generally assumed prograde origin for other berthierine occurrences.

Electroacoustic measurements at 1 MHz, using the Electro-Sonic Amplitude (ESA), on a kaolinite suspension provide a ready method for following the adsorption of hydrolyzable metal ions onto the clay surface. Co2+, Cd2+ and Cu2+ ions show similar behavior: The initially negative surface becomes less negative, approaches zero, and may become positive at pH values around neutral, depending on the initial metal concentration. At higher pH, electrokinetic potential goes through a maximum. If the surface has become positive, it becomes less so; and at still higher pH values it may become negative again, depending on the metal ion concentration. The behavior can be interpreted using the model proposed by James and Healy.

Phenol (benzenol) oxidation by three synthetic manganese oxides (buserite, manganite, and feitknechtite) has been studied in aerated, aqueous, acidified suspensions. The rate of reaction was pH dependent. Oxidation was greatly enhanced below pH 4, when diphenoquinone and p-benzoquinone were identified as the first products. Initial reaction rate was correlated with standard reduction potential (E°) of the oxides following the order: feitknechtite > manganite > buserite. A more gradual process of phenol oxidation after the initial reaction was influenced by electrochemical properties of the solution. High soluble manganese activity and increase in pH adversely affected reaction rates. Thus, the reactivity of the oxides was related to their stability and possibly the ability to readsorb Mn(II), following the order: buserite > manganite > feitknechtite. The results indicate that thermodynamic and electrochemical data for oxides and phenols are useful in predicting under which conditions phenols can be oxidized by a given system.

The effect of anions on clay dispersion and the hydraulic conductivity (HC) of clay-sand mixtures has received little attention. This study investigates the effect that adding small amounts of anions has on the dispersivity and HC of reference clays. Mixtures of 3 and 6 g 100 g−1 kaolinite, smectite, and illite with quartz sand were packed in columns. The columns were saturated with Ca and then leached with 1 molc m−3 of one of the following organic and inorganic Na salts: chloride, hydroxide, EDTA, silicate, citrate, formate, oxalate, hexametaphosphate, orthophosphate, tartrate, or humate. Changes in HC and clay concentration in the effluent were measured and clay dispersion was evaluated as a function of the various anions added. In the kaolinite clay-sand mixtures, a significant amount of clay was observed in the effluent for all anions tested, and the HC increased above its original value. The HC of smectite clay-sand mixtures decreased following the addition of the various anions. Dispersed clay appeared in the effluent only upon addition of citrate or hexametaphosphate. In the latter two cases, the HC started to increase once maximum clay concentration appeared in the effluent. Clay concentration in the effluent of smectite was one order of magnitude lower than that of kaolinite. Illite clay-sand mixtures showed dispersion behavior intermediate between smectite and kaolinite but behaved in the same way as kaolinite with respect to HC changes.