Influence of copper ions and calcium ions on adsorption of CMC on chlorite

The effects of copper ions and calcium ions on the depression of chlorite using CMC（carboxymethyl cellulose） as a depressant were studied through flotation tests,adsorption measurements,ζ potential tests and co-precipitation experiments.The results show that the electrostatic repulsion between the CMC molecules and the chlorite surfaces hinders the approach of the CMC to the chlorite while the presence of copper ions and calcium ions enhances the adsorption density of CMC.The action mechanisms of these two types of ions are different.Calcium ions can not adsorb onto the mineral surfaces,but they can interact with the CMC molecules,thus reducing the charge of the CMC and enhancing adsorption density.Copper ions can adsorb onto the mineral surfaces,which facilitates the CMC adsorption through acid/base interaction.The enhanced adsorption density is also attributed to the decreased electrostatic repulsion between the CMC and mineral surfaces as copper ions reduce the surface charge of both the mineral surfaces and the CMC molecules.

Chlorite cement and its effect on the reservoir quality of sandstones from the Panyu low-uplift,Pearl River Mouth Basin

Based on porosity and permeability measurements, mercury porosimetry measurements, thin section analyses, SEM observations, X-ray diffraction （XRD） analysis and granulometric analyses, diagenetic features of reservoir sandstones taken from the Zhuhai formation in the Panyu low-uplift of the Pear River Mouth Basin were examined. This study shows that chlorite cements are one of the most important diagenetic features of reservoir sandstones. The precipitation of chlorite was controlled by multiple factors and its development occurred early in eo-diagenesis and continued till Stage A of middle diagenesis. The precipitation of chlorite at the early stage was mainly affected by the sedimentary environment and provenance. Abundant Fe- and Mg-rich materials were supplied during the deposition of distributary channel sediments in the deltaic front setting and mainly in alkaline conditions. With the burial depth increasing, smectite and kaolinite tended to be transformed into chlorite. Smectite cements were completely transformed into chlorite in sandstones of the studied area. Volcanic lithics rich in Fe and Mg materials were dissolved and released Fe2＋ and Mg 2＋ into the pore water. These cations precipitated as chlorite cements in middle diagenesis in an alkaline diagenetic environment. Chlorite coatings acted as porosity and permeability, thus helping preserve cements in the chlorite cemented sandstones. The reservoir quality of chlorite cemented sandstones is much better than sandstones without chlorite cements. Chlorite cements play an important role in the reservoir evolution that was mainly characterized by preserving intergranular porosity and forming better pore-throat structures of sandstones.

Selective depression action of taurine in flotation separation of specularite and chlorite

Chlorite,as the most representative gangue mineral associated with specularite,of which the separation of these two minerals is difficult.This paper investigated the depression effect of taurine on specularite/chlorite separation via flotation experiments,adsorption tests,contact angle measurements,Zeta potential detection,FT-IR measurements,and XPS analyses.The results of single mineral flotation indicated that chlorite could be depressed selectively by taurine with the recovery of less than 30%,but the floatability of specularite remains high with recovery rate of 81.77%at pH 10.The artificial mixed mineral flotation results confirmed the effectiveness of taurine as a depressant.Surface adsorption,contact angle,and Zeta potential detection revealed taurine primarily adsorbs on the chlorite surface,which hampered the DDA’s subsequent adsorption and results in the chlorite’s poor floatability.The FT-IR spectra and XPS analyses provided further proof that taurine adsorbed on chlorite surface as an electron donor,and part of the electrons transferred from the sulfonic acid group of taurine to metal ions during the adsorption process.In addition,the hydrogen bond between amino-group of taurine and O ions in chlorite surface was also formed in the adsorption process.Finally,optimized adsorption configurations of taurine on chlorite surfaces were proposed.

Origin and controlling factors of chlorite coatings—an example from the reservoir of T_3x Group of the Baojie area,Sichuan Basin,China

The study of the chlorite coatings always attracts scholars in China and other countries because the chlorite coatings play an important role in the preservation of residual primary pores in sandstone reservoirs.At present,the study of the origin and the controlling factors is relatively few.The occurrence,time of formation,genesis,controlling factors,and the mechanism of chlorite coatings inhibiting quartz overgrowths were studied in detail with thin section and SEM analysis.Samples were from the sandstone reservoirs of the T3x Group in the Baojie area,the transitional zone from the middle to the south of Sichuan Basin.The results indicate that the chlorite coatings on the walls of the pore spaces are oriented perpendicular to grain surfaces in the form of isopachous(even-thickness) grain-coating,while the chlorite coatings at the contacts between adjacent detrital grains are arranged with a preferred orientation tangential to the surface of detrital grains.The chlorite coatings were formed in the eogenetic stage.They were formed by recrystallization of Fe-rich clay films during the syndepositional period,and chlorite cements would be recrystallized after the coatings’ formation.The formation of chlorite coatings was mainly controlled by the depositional environment,provenance conditions,and diagenetic environment.The presence of chlorite coatings could result in the preservation of primary pores in deeply buried sandstone reservoirs by effectively inhibiting quartz overgrowths and the development of compaction and pressure solution.

Investigation of methane adsorption on chlorite by grand canonical Monte Carlo simulations

In this paper, the methane adsorption behaviours in slit-like chlorite nanopores were investigated using the grand canonical Monte Carlo simulation method, and the influences of the pore sizes, temperatures, water, and compositions on methane adsorption on chlorite were discussed. Our investigation revealed that the isosteric heat of adsorption of methane in slit-like chlorite nanopores decreased with an increase in pore size and was less than 42 kJ/mol, suggesting that methane adsorbed on chlorite through physical adsorption. The methane excess adsorp- tion capacity increased with the increase in the pore size in micropores and decreased with the increase in the pore size in mesopores. The methane excess adsorption capacity in chlorite pores increased with an increase in pressure or decrease in pore size. With an increase in temperature, the isosteric heats of adsorption of methane decreased and the methane adsorption sites on chlorite changed from lower- energy adsorption sites to higher-energy sites, leading to the reduction in the methane excess adsorption capacity. Water molecules in chlorite pores occupied the pore wall in a directional manner, which may be related to the van der Waals and Coulomb force interactions and the hydrogen bonding interaction. It was also found that water molecules existed as aggregates. With increasing water content, the water molecules occupied the adsorption sites and adsorption space of the methane, leading to a reduction in the methane excess adsorption capacity. The excess adsorption capacity of gas on chlorite decreased in the following order： carbon dioxide 〉 methane 〉 nitrogen. If the mole fraction of nitrogen or carbon dioxide in the binary gas mixture increased, the mole fraction of methane decreased, methane adsorption sites changed, and methane adsorption space was reduced, resulting in the decrease in the methane excess adsorption capacity.

Formation mechanisms and sequence response of authigenic grain-coating chlorite: evidence from the Upper Triassic Xujiahe Formation in the southern Sichuan Basin, China

Authigenic grain-coating chlorite is widely distributed in the clastic rocks of many sedimentary basins around the world. These iron minerals were mainly derived from flocculent precipitates formed when rivers flow into the ocean, especially in deltaic environments with high hydrodynamic conditions. At the same time, sandstone sequences with grain-coating chlorites also tend to have relatively high glauconite and pyrite content. EPMA composition analysis shows that glauconites with ‘‘high Al and low Fe’’ content indicate slightly to semi-saline marine environments with weak alkaline and weakly reducing conditions. By analyzing the chlorite-containing sandstone bodies of the southern Sichuan Xujiahe Formation, this study found that chlorite was mainly distributed in sedimentary microfacies, including underwater distributary channels, distributary channels, shallow lake sandstone dams, and mouth bars. Chlorite had a tendency to form in the upper parts of sandstone bodies with signs of increased base level, representing the influence of marine（lacustrine）transgression. This is believed to be influenced by megamonsoons in the Middle and Upper Yangtze Region during the Late Triassic Epoch. During periods of abundant precipitation, river discharges increased and more Fe particulates flowed into the ocean（lake）. In the meantime,increases or decreases in lake level were only affected byprecipitation for short periods of time. The sedimentary environment shifted from weakly oxidizing to weak alkaline, weakly reducing conditions as sea level increased, and Fe-rich minerals as authigenic chlorite and glauconite began to form and deposit.

Effect of solution conditions on depression of chlorite using CMC as depressant

The effect of solution conditions on the depression of chlorite using CMC (carboxymethyl cellulose) as depressant was studied through flotation tests and adsorption measurements. Flotation and adsorption tests were first studied as a function of initial solution conditions. The results show that electrostatic repulsion between CMC molecules and chlorite surface hinders the approach of the CMC molecules to the chlorite surface and CMC adsorbs to a great extent at high ionic concentration (10-4 mol/L ions as opposed to 0 mol/L ions) or low pH (3 as opposed to 9). The enhanced adsorption density is attributed to the decreased electrostatic repulsion between CMC and mineral surface. The solution condition that yielded the lowest initial adsorbed amount (0 mol/L ions, pH 9) was used as a reference to investigate the response of the adsorbed CMC layer to a switch in solution conditions after adsorption. The two kinds of solution switches (reducing the solution pH or increasing ionic concentration) result in an increased depression effect of CMC on chlorite flotation, as a result of conformational change of CMC pre-adsorbed layer. The change in the flotation recovery of the CMC-coated chlorite following the solution switches is reversible.

Ordinary Toxicity of Chlorine Dioxide and By-products Chlorite and Chlorate in Water

Acute toxicity and accumulated toxicity of chlorine dioxide (ClO2) and by-products chlorite (ClO2-) and chlorate (ClO3-) in water acted on mice are studied by the method of Horn and accumulation coefficient. Subchronic toxicity of the mixture of ClO2 and ClO2-and ClO3- in water acted on rat is studied though feeding test for 90 days, including statistical analysis of variance on weight gaining, food utilization efficiency,index of blood and serum,liver (or kidney) to body weight ratio, and histopathological examination on liver and kidney. The results show that aqueous solution of ClO2, NaClO2 and NaClO3 ( with the concentration of 276.5 mg/L, 200 mg/L and 200 mg/L respectively) and the mixed aqueous solution of ClO2 with the concentration of 553 mg/L are actually non-poisonous , and non-cumulative aqueous solution as well.

A novel, simple and sensitive resonance scattering spectral method for the determination of chlorite in water by means of rhodamine B

A new resonance scattering method was proposed for the determination of chlorite, basing on the resonance scattering effect of rhodamine dye. In HCl-sodium acetate buffer solution, chlorite oxidizes 1- into 12 and the reaction of 12 and excess 1- results in If. It is respectively combined with rhodaminc dyes, including rhodamine B （RhB）, butyl rhodamine B （b-RhB）, rhodamine G （RhG） and rhodamine S （RhS）, to form association complex particles, which exhibit stronger resonance scattering （RS） effect at 400 nm. The chlorite concentration of ClO2 in the range of 0.00726-0.218 μg/ml, 0.0102-0.292 μg/ml, 0.00726-0.145 μg/ml and 0.0290- 0.174 μg/ml is respectively linear to the RS intensity of association complex particle systems at 400 nm for the RhB, b-RhB, RhG and RhS. The detection limits of the four systems were respectively 0.00436, 0.00652, 0.00580 and 0.01450μg/ml ClO2^-. In the four systems, the RhB system possesses good stability and high sensitivity. It has been applied to the analysis of chlorite in wastewater with satisfactory results.

Geochemistry and Tectonic Significance of Chlorite Amphibolite in Nanfen BIF, Benxi Area, Northeastern China

Benxi area, Northeastern China, is the main distribution area of Archean BIF-hosted iron deposits in China. In this area, Nanfen iron deposit is well known as the largest open-pit iron deposit not only in China but also in Asia. So far, the tectonic nature during Archean BIF formation period in Benxi area has been long disputed and the tectonic setting of Nanfen BIF had not been found. In this study, the geochemical characters of chlorite amphibolites closely associated with BIF have been investigated for the tectonic environment of Nanfen BIF. Chlortie amphibolites show the geochemical affinity to the back-arc basin basalt (BABB), indicating that the tectonic environment of Nanfen BIF is the back-arc basin. In conjunction with geological evidence of other BIFs at Benxi area, it is identified that BIF in Benxi area might be formed in the subduction-related back-arc basin, which provides a favorable sedimentary environment of Algoma-type BIF.

Preparation of porous silica from natural chlorite via selective acid leaching and its application in methylene blue adsorption

In this study,porous silica with high surface area was prepared through selective leaching of thermally activated chlorite in HCl solution.In the process,chlorite was activated by pre-calcining treatment,then activated components(MgO,Al_(2)O_(3),and Fe_(2)O_(3))were selectively leached by acid solution,resulting in the formation of nanopores in situ.The morphology,structure,surface area and pore-size distribution of the material were characterized by XRD,TG/DSC,^(27)Al MAS NMR,SEM,TEM and N2 adsorption−desorption isotherms.The highest specific surface area(SBET=333 m^(2)/g)was obtained by selectively leaching the 600℃ calcined chlorite from 3 mol/L HCl at 90℃ for 2 h.The pore sizes and specific surface areas can be controlled by calcination and leaching conditions.The ^(27)Al MAS NMR spectra of the samples revealed the relationship between structural transformation and the selective acid leaching properties of thermal-activated chlorite,demonstrating that AlVI transfers into AlV when chlorite changes into activated chlorite during thermal activation,and the coordinations of Al has a significant effect on acid solubility of chlorite.The as-prepared porous silica showed favorable adsorption abilities with capacity of 148.79 mg/g for methylene blue at pH of about 7 and temperature of 25℃,indicating its promising potential in adsorption application.

Mineralogical Characteristics and Short-wave Infrared Spectra of Chlorite as Indicators of Hydrothermal Centers: A Case Study of the Giant Porphyry Copper-Molybdenum Deposit at Qulong, Tibet

The Qulong deposit in Tibet is one of the largest porphyry copper-molybdenum deposits in China. We used short-wave infrared(SWIR) spectroscopy to examine the spectral characteristics of the extensively developed chlorite in this deposit. X-ray diffraction and electron microprobe analyses were used for phase identification and to obtain the chemical composition, ion substitution relationships, and formation environment of the chlorite. SWIR spectral parameters were applied to detect the hydrothermal centers. The results indicate that the wavelength of the absorption feature for Qulong chlorite Fe-OH(Pos2250) range from 2240 to 2268.4 nm;the chlorite substitution relationships are dominated by Mg-Fe substitution at the octahedral sites together with Al;-Si substitution at the tetrahedral sites;the chlorite formation temperatures range within the medium-low temperature hydrothermal alteration range from 164 to 281°C, with an average value of 264℃;the wavelength of the chlorite peak position for Fe-OH(2250 nm) absorption and its chemical composition are positively correlated with Al^(Ⅵ), Fe + Al^(Ⅵ), Fe/(Fe + Mg), Fe, and Fe + Al^(Ⅳ)but negatively correlated with Mg and Mg/(Fe + Mg);and the wavelength associated with the chlorite Fe-OH(2250 nm) absorption feature is positively correlated with the temperature at which the chlorite formed. These correlations indicate that more Fe and Al^(Ⅵ) ions and fewer Mg ions at the octahedral sites of chlorite lead to a longer the wavelength of the chlorite Fe-OH(2250 nm) absorption feature and a higher chlorite formation temperature. The wavelength of the Qulong chlorite Fe-OH(2250 nm) absorption feature(>2252 nm) can thus serve as an exploration indicator to guide the detection of hydrothermal centers in porphyry copper deposits. The results of the study indicate that the mineralogical and SWIR spectral characteristics of chlorite are significant indicators for locating hydrothermal centers within porphyry deposits.

Antimicrobial Activity of Acidified Sodium Chlorite and Cell Free Culture Supernatent of Lactic Acid Bacteria against <i>Salmonella</i>Typhimurium

Most methods used by food industries to decontaminate eggs involve washing of egg surface with various chemicals. In this study, the effectiveness of two organic decontaminants viz., acidified sodium chlorite (ASC) and cell free culture supernatant (CFCS) of two lactic acid bacteria (Lactobacillus plantarum and Pediococcus cerevisiae) was evaluated for the decontamination of spiked Salmonella Typhimurium on chicken egg shell surface. Acidified sodium chlorite at 100 μl/L concentration with the contact time of 20 min completely inhibited S. Typhimurium on egg shell surface while at 50 μl/L concentration 1 - 2 log10 units reduction was observed in counts of S. Typhimurium as compared to control group. Likewise, CFCS of P. cerevisiae completely inhibited the growth of S. Typhimurium on 30 min contact, whereas L. plantarum and combination of both were revealed significant reduction in the counts of S. Typhimurium counts.

Magnesium isotopes of chlorite-rich hydrothermal sediments in the Okinawa Trough and indications for Mg cycle

Seafloor hydrothermal systems play a significant role in the oceanic Mg cycle due to ubiquitous deposits of secondary Mg-rich clays during the strong fluid-rock reactions.However,the magnitude of net Mg enrichment and Mg isotopic fractionation,particularly within the medium-high temperature hydrothermal systems in felsic-hosted settings,are not well studied yet.Here we report elemental and isotopic compositions of Mg in hydrothermal chlorite-rich sediments,volcanic materials,and terrigenous sediments collected during the IODP Expedition 331 drilled to the thick sediment-covered and felsic-hosted middle Okinawa Trough(Iheya North Knoll) in the West Pacific.We investigate the sources of Mg in chlorite and Mg isotopic behavior at medium-high temperature hydrothermal alteration.After 1 mol/L HCl leaching,Mg isotopic compositions of chlorite-rich sediments present overall similar values in the residual fractions and bulk samples albeit with slightly higher values in the leachates.Mineralogical differentiation primarily determines the Mg isotopic compositions,showing that siliciclastic residues have slightly higher δ^(26) Mg values than the leachates dominated by carbonates and oxides/hydroxides.Significant Mg isotopic fractionation happened in the medium-high temperature(~150°C to 260°C) felsic-hosted hydrothermal system,with Δ^(26)MgChl-SW ranging from 0.15‰ to 0.71‰ and yielding a negative correlation with temperature.This observation suggests the preferential incorporation of heavy Mg isotopes by the secondary chlorite precipitation.We infer that the medium-high temperature hydrothermal systems can take up about 8–14% of riverine input of Mg in the arc and back-arc regions.Incomplete removal of aqueous Mg in porewater and vent fluids by the medium-high temperature hydrothermal alterations in the arc and back-arc basins provides constraints on the Mg budget and isotopic composition of seawater.

Iron species activating chlorite:Neglected selective oxidation for water treatment

Chlorite(ClO_(2)-)is the by-product of the water treatment process carried out using chlorine dioxide(ClO_(2))as an effective disinfectant and oxidant;however,the reactivation of ClO_(2)
has commonly been overlooked.Herein,it was unprecedentedly found that ClO_(2)
could be activated by iron species(Feb:Fe0,FeII,or FeIII),which contributed to the synchronous removal of ClO_(2)
and selective oxidative treatment of organic contaminants.However,the above-mentioned activation process presented intensive Ht-dependent reactivity.The introduction of Feb significantly shortened the autocatalysis process via the accumulation of Cl
or ClO
during the protonation of ClO_(2)
driven by ultrasonic field.Furthermore,it was found that the interdependent high-valent-Fe-oxo and ClO_(2),after identification,were the dominant active species for accelerating the oxidation process.Accordingly,the unified mechanisms based on coordination catalysis([FeN(H_(2)O)a(ClOxm)b]nt-P)were putative,and this process was thus used to account for the pollutant removal by the Feb-activated protonated ClO_(2).This study pioneers the activation of ClO_(2)
for water treatment and provides a novel strategy for“waste treating waste”.Derivatively,this activation process further provides the preparation methods for sulfones and ClO_(2),including the oriented oxidation of sulfoxides to sulfones and the production of ClO_(2) for on-site use.

Evolution of chlorite composition in the Paleogene prototype basin of Jiyang Depression, Shandong, China, and its implication for paleogeothermal gradient

The Dongying Basin, Huimin Basin, and Zhanhua Basin constitute the Jiyang Depression in Shandong Province. They are major oil and gas exploring districts within the depression. Through reconstructions of the paleotemperature of the three basins facilitated with the chlorite geothermometry, the thermal history of the Paleogene prototype basin in Jiyang Depression and its geologic significance were explored. This study reveals that the Si^(4+) component in chlorites reduces gradually as its buried depth increases, while the AI~Ⅳ component increases accordingly. The chlorite type changes from silicon-rich diabantite to silicon-poor ferroamesite and prochlorite. The prochlorite in this district only appears in the deep buried depth, high temperature, and relatively old stratigraphies; while the diabantite appears in the shallower buried, low temperature, and newly formed strata; the ferroamesite exists in the conditions between prochlorite and diabantite formation. The diagenetic temperatures of the chlorites in these Paleogene basins are 171 — 238℃ for the Dongying Basin, 160—202℃ for the Huimin Basin, and 135—180℃ for the Zhanhua Basin. The differences of the chlorite diagenetic temperatures in the three basins were controlled by the duration time of the structural depressing processes. Higher temperature indicates longer depression time. The relationship between the chlorite diagenetic temperature and its buried depth indicates that the average paleogeothermal gradient is about 38.3℃ /km in the Paleogene prototype basin of Jiyang Depression. It was higher than the present geothermal gradient (29—30℃/km). This phenomenon was attributed to the evolution of the structural dynamics in the depression basin.

Decoding Subsurface Secondary Mineralisation and its Impact on Cohesive Strength:An Outcome of the Deep Scientific Drilling Program in the Koyna-Warna Seismogenic Region,Western India

The Koyna-Warna seismogenic region overlying the Deccan volcanic province of Western India has been experiencing the recurrence of earthquakes since 1967 soon after the impoundment of the Koyna Dam.A large number of small to medium-magnitude shallow focus earthquakes(>100,000)have been detected in this intraplate region during the last six decades.In the present study,the core samples recovered from the borehole‘KBH3’drilled upto 1134 m depth in the pre-Deccan granitoids basement rocks of this region have been subjected to mineralogical and geochemical studies.

Effects of reductive inorganics and NOM on the formation of chlorite in the chlorine dioxide disinfection of drinking water

Chlorine dioxide(ClO_(2))disinfection usually does not produce halogenated disinfection byproducts,but the formation of the inorganic by-product chlorite(ClO^(–)_(2))is a serious consideration.In this study,the ClO^(–)_(2)formation rule in the ClO_(2)disinfection of drinking water was investigated in the presence of three representative reductive inorganics and four natural organic matters(NOMs),respectively.Fe^(2+)and S^(2–)mainly reduced ClO_(2)to ClO^(–)_(2)at low concentrations.When ClO_(2)was consumed,the ClO^(–)_(2)would be further reduced by Fe^(2+)and S^(2–),leading to the decrease of ClO^(–)_(2).The reaction efficiency of Mn^(2+)with ClO_(2)was lower than that of Fe^(2+)and S^(2–).It might be the case that Mn O 2 generated by the reaction between Mn^(2+)and ClO_(2)had adsorption and catalytic oxidation on Mn^(2+).However,Mn^(2+)would not reduce ClO^(–)_(2).Among the four NOMs,humic acid and fulvic acid reacted with ClO_(2)actively,followed by bovine serum albumin,while sodium alginate had almost no reaction with ClO_(2).The maximum ClO^(–)_(2)yields of reductive inorganics(70%)was higher than that of NOM(around 60%).The lower the concentration of reductive substances,the more ClO^(–)_(2)could be produced by per unit concentration of reductive substances.The results of the actual water samples showed that both reductive inorganics and NOM played an important role in the formation of ClO^(–)_(2)in disinfection.

Impact of chlorites on the wettability of tight oil sandstone reservoirs in the Upper Triassic Yanchang Formation,Ordos Basin,China

Wettability is an essential property of reservoirs that is of great importance for enhancing oil recovery(EOR)and oil migration.The wettability of reservoirs is generally believed to be strongly affected by mineral compositions but it is not always the case.An integrated study of petrography and wettability was carried out to determine the impact of chlorite minerals on the wettability of the sandstone reservoirs in the Upper Triassic Yanchang Formation.Chlorites are found to be commonly present in the reservoir sandstones as detrital grains,rim-shaped cements,and biotite-chloritized forms with the pore peripheries being largely coated by chlorite,which is the main mineral in direct contact with pores.At pore scale,the wetting state of chlorites can either be oil-wet or water-wet in the tight sandstone reservoirs depending on wettability alteration by oil charge.Chlorites in contact with pores occupy a large of proportions of oil-wet pore walls and are crucial for the formation of oil-wetting state of reservoir sandstones.At core scale,the contents of chlorites in direct contact with pores do not correlate well with the AmottHarvey index due to other factors such as heterogeneity,oil-bearing degrees of samples.

THE ELECTRON MICROSCOPY STUDY ON THE MIXED LAYER OF ILLITE AND CHLORITE

Clay minerals having the same type of octahedral layer commonly occur as mixed layers. With the application of electron microscopy in day mineralogy, it is recognized that clay minerals which have different octahedral sheets can also form mixed layers, such as the mixed layer of illite and chlorite which has been well studied. However, there are different opinions on its origin. Based on the study of transmission electron microscopy (TEM)