Mixed Compounds Research Articles

The Use of Compound Words in the Guardian News Website

This study aims to find out the types of compound words and formation of compound words found in the Guardian News Websites. The data were classified and analyzed by applying the theory from Delahunty & Garvey (2010) and supported by the theory from McCarthy (2002), about the types and the formation of compound words. This study applied descriptive qualitative research and the data were collected using observation and documentation technique. The results of this study found that there were 164 compound words in fourteen selected news articles on the Guardian News Website. The first result showed that there are four types of compound words found in this study: 101 (62%) compound nouns, 33 (20%) compound verbs, 25 (15%) compound adjectives, and 5 (3%) prepositions compound. The second result showed that there are four types of compound word formation: 103 (63%) closed compound, 29 (18%) open compound, 22 (13%) hyphenated compound, and 10 (6%) mixed compound.

Effect of Fermi surface topology change on the Kagome superconductor CeRu2 under pressure

The cubic Laves phase compound CeRu2 with a Kagome substructure of Ru has been investigated to understand myriad fascinating phenomena resulting from competition among its various physical and geometric features. Such phenomena include flat bands, van Hove singularities, Dirac cones, reentrant superconductivity, magnetism, the Fulde–Ferrell–Larkin–Ovchinnikov state, valence fluctuations, time-irreversible anisotropic s-state superconductivity, etc. Extensive studies have thus been carried out since 1958 when the highly unusual coexistence of superconductivity and ferromagnetism was proposed for the mixed compounds (Ce,Gd)Ru2. Activity has accelerated in recent years due to increasing interest in topological states in superconductors. However, there has been little investigation of the mutual influence of these fascinating states. Therefore, we systematically investigated the superconductivity and possible Fermi surface topological change in CeRu2via magnetic, resistivity, and structural measurements under pressure up to ∼168 GPa. An unusual phase diagram that suggests an intriguing interplay between the compound's superconducting order and Fermi surface topological order has been constructed. A resurgence in its superconducting transition temperature was observed above 28 GPa. Our experiments have identified a structural transition above 76 GPa and a few tantalizing phase transitions driven by high pressure. Our high-pressure results further suggest that superconductivity and Fermi surface topology in CeRu2 are strongly intertwined.

Asymmetric by Design: Heteroleptic Coordination Compounds with Redox-Active Dithiolene and 1,2,4,5-Tetrakis(isopropylthio)benzene Ligands.

The 1,2,4,5-tetrakis(alkylthio)benzenes are redox-active organosulfur molecules that support oxidation to a stable radical cation. Their utility as ligands for the assembly of multimetal complexes with tailored functionality/property is unexamined. Here, 1,2,4,5-tetrakis(isopropylthio)benzene (tptbz, 1) is shown to bind PdCl2 at either one end, leaving the other open, or at both ends to form centrosymmetric [Cl2Pd(tptbz)PdCl2], 4. Ligand metathesis between Na2[(N≡C)2C2S2] (Na2mnt) and [Cl2M(tptbz)] (M = Pd, 2; M = Pt, 3) yields [(mnt)M(tptbz)] (M = Pd, 5; M = Pt, 6), but an alternative route involving transmetalation with [(mnt)SnMe2] delivers substantially greater yield. The mixed dithiolene-dithioether compound [(Ph2C2S2)Pt(tptbz)] (8) is formed by a similar transmetalation protocol using [(Ph2C2S2)SnnBu2]. Compounds 5, 6, and 8 are the first such heteroleptic complexes prepared by deliberate synthesis. The cyclic voltammetry of 8 reveals anodic waves at +0.14 and +0.97 V vs Fc+/Fc, which are attributed to successive dithiolene oxidation processes. While oxidized at +0.73 V as a free ligand, the redox-active MO of tptbz is pushed to a higher potential upon coordination to Pt2+ and is inaccessible. Calculations of the structures of [8]+ and of [((Cl2-3,5-C6H3)2C2S2)Pt(tptbz)]+ show that, in the latter, the dithiolene MOs are drawn down in energy into proximity with the tptbz MOs.

Study on detection of intracerebral hemorrhage based on frequency difference of permittivity

Introduction: Current detection of intracerebral hemorrhage (ICH), whether employing Electrical Capacitance Tomography (ECT) or other electrical imaging techniques, rely on time-difference measurements. The time-difference methods necessitate baseline measurements from the patient in a non-hemorrhagic state, which is impractical to obtain, rendering rapid detection of ICH unfeasible.Methods: This study introduces a novel approach that capitalizes on the distinct dispersion characteristics of the permittivity in brain tissue and the spectral variance of the permittivity between blood and other brain components. Specifically, the frequency-dependent variations in the permittivity are employed to achieve absolute detection of ICH, thereby eliminating the need for non-hemorrhagic baseline data. The methodology entails identification of two frequency points that the frequency-dependent variation in the permittivity at these two frequency points manifest the maximal difference between blood and other brain tissues. Subsequently, this permittivity differential at the two identified frequency points is utilized for hemorrhage detection. Experimental measurements were conducted using an impedance analyzer and a parallel plate capacitor to capture the capacitance in four single-component substances—distilled water, sheep blood, isolated pig fat, and isolated pig brain—as well as three mixed blood compounds—distilled water enveloping sheep blood, pig fat encapsulating sheep blood, and pig brain surrounding sheep blood—across a frequency range of 10 kHz to 20 MHz.Results: The results show that in different frequency bands, it is indeed possible to distinguish single-component substances from mixed substances by the frequency difference of capacitance variation. Comparative analysis reveals that the 1 MHz to 5 MHz frequency range is most effective for detecting blood in distilled water. For blood detection in pig fat, a 10 kHz to 1 MHz frequency range is identified as optimal, while a 10 kHz to 0.5 MHz frequency range is advantageous for blood detection in pig brain tissue.Discussion: The findings confirm that absolute detection of ICH is achievable through frequency-dependent variations in the permittivity. However, this necessitates the identification of the frequency band manifesting the largest difference of frequency-dependent variation between single-component and mixed substances. The study acknowledges limitations primarily due to the use of anticoagulant-altered sheep blood, which exhibits permittivity divergent from those of natural blood. Additionally, the in vitro pig fat and pig brain samples, having been subjected to freeze-thaw cycles, also demonstrate permittivity unrepresentative of in vivo tissue.

1,10‐Phenanthroline‐Based Octahedra Induced by Protonation of a Nitrogen Atom: Structures and Emission Properties

AbstractAlthough a few metal‐free octahedral compounds based on nitrogen‐containing ligands are known, the realization of mixed ligand compounds remains difficult. To obtain an improved understanding of this class of compounds, two new octahedral compounds, [(tmphenH)(phen)]PF6, and [(tmphenH)(tmphen)]PF6 (where tmphen=3,4,7,8‐tetramethyl‐1,10‐phenanthroline and phen=1,10‐phenanthroline), were synthesized. The relationship between the emission properties, as evaluated using experimental measurements and theoretical calculations, and structures of the protonated compounds was studied. In addition, differences between the atomic charge distributions and geometries in the ground and singlet excited states were investigated using density functional theory calculations. Both [(tmphenH)(phen)]PF6 and [(tmphenH)(tmphen)]PF6 formed hydrogen‐bonded octahedrons in acetonitrile solution, even in the excited state. However, the hydrogen bonding in [(tmphenH)(phen)]PF6 was weak and thermal vibrations decreased the emission intensity. In contrast, the additional methyl substituents in [(tmphenH)(tmphen)]PF6 suppressed thermal vibrations, resulting in a higher emission intensity.

Nonlinear effect of NOx concentration decrease on secondary aerosol formation in the Beijing-Tianjin-Hebei region: Evidence from smog chamber experiments and field observations

During the COVID-19 lockdown in the Beijing-Tianjin-Hebei (BTH) region in China, large decrease in nitrogen oxides (NOx) emissions, especially in the transportation sector, could not avoid the occurrence of heavy PM2.5 pollution where nitrate dominated the PM2.5 mass increase. To experimentally reveal the effect of NOx control on the formation of PM2.5 secondary components (nitrate in particular), photochemical simulation experiments of mixed volatile organic compounds (VOCs) under various NOx concentrations with smog chamber were performed. The proportions of gaseous precursors in the control experiment were comparable to ambient conditions typically observed in the BTH region. Under relatively constant VOCs concentrations, when the initial NOx concentration was reduced to 40% of that in the control experiment (labelled as NOx,0), the particle mass concentration was not significantly reduced, but when the initial NOx concentration decreased to 20 % of NOx,0, the mass concentration of particles as well as nitrate and organics showed a sudden decrease. A “critical point” where the mass concentration of secondary aerosol started to decline as the initial NOx concentration decreased, located at 0.2–0.4 NOx,0 (or 0.18–0.44 NO2,0) in smog chamber experiments. The oxidation capacity and solar radiation intensity played key roles in the mass concentration and compositions of the formed particles. In field observations in the BTH region in the autumn and winter seasons, the “critical point” exist at 0.15–0.34 NO2,0, which coincided mostly with the laboratory simulation results. Our results suggest that a reduction of NOx emission by >60% could lead to significant reductions of secondary aerosol formation, which can be an effective way to further alleviate PM2.5 pollution in the BTH region.

Use of the Peroxide Method for Vanadium Activation to Obtain Mixed Keggin-Type Heteropoly Compounds

Use of the Peroxide Method for Vanadium Activation to Obtain Mixed Keggin-Type Heteropoly Compounds

Ab initio crystal structures and relative phase stabilities for the aleksite series, PbnBi4Te4Sn+2.

Density functional theory methods are applied to crystal structures and stabilities of phases from the aleksite homologous series, PbnBi4Te4Sn+2 (n = homologue number). The seven phases investigated correspond to n = 0 (tetradymite), 2 (aleksite-21R and -42R), 4 (saddlebackite-9H and -18H), 6 (unnamed Pb6Bi4Te4S8), 8 (unnamed Pb8Bi4Te4S10), 10 (hitachiite) and 12 (unnamed Pb12Bi4Te4S14). These seven phases correspond to nine single- or double-module structures, each comprising an odd number of atom layers, 5, 7, (5.9), 9, (7.11), 11, 13, 15 and 17, expressed by the formula: S(MpXp+1)·L(Mp+1Xp+2), where M = Pb, Bi and X = Te, S, p ≥ 2, and S and L= number of short and long modules, respectively. Relaxed structures show a and c values within 1.5% of experimental data; a and the interlayer distance dsub decrease with increasing PbS content. Variable Pb-S bond lengths contrast with constant Pb-S bond lengths in galena. All phases are n-fold superstructures of a rhombohedral subcell with c/3 = dsub*. Electron diffraction patterns show two brightest reflections at the centre of dsub*, described by the modulation vector qF = (i/N) · dsub*, i = S + L. A second modulation vector, q = γ · csub*, shows a decrease in γ, from 1.8 to 1.588, across the n = 0 to n = 12 interval. The linear relationship between γ and dsub allows the prediction of any theoretical phases beyond the studied compositional range. The upper PbS-rich limit of the series is postulated as n = 398 (Pb398Bi4Te4S400), a phase with dsub (1.726 Å) identical to that of trigonal PbS within experimental error. The aleksite series is a prime example of mixed layer compounds built with accretional homology principles.

Statistical inference for mixed jump processes by Markov switching model with application to identify seismicity levels

Describing the non-stationarity of mixed stochastic jump processes presents a formidable challenge. This study employs a mixed compound Poisson process by Markov switching model (CPMSM) to address the issue of overdispersed data of random jumps. The Poisson rate is governed by a continuous-time Markov chain in this model. By assuming independence of the compound Poisson process and jump sizes, we present a generalized algorithm to estimate the parameters of CPMSM and try to predict the future behavior of this stochastic system. To investigate the potential application of this model and the accuracy of our algorithm, we provide a numerical simulation example in the context of the auto insurance payout scenario. The results suggest that CPMSM is an effective method of describing jump behavior controlled by random counts with mode switching via a Markov chain. Furthermore, we demonstrate a specific application of this model in identifying seismicity levels of Greek earthquake data and identify four hidden states. Finally, we compare its fitting effectiveness with the ETAS model using two public earthquake datasets in Japan and Iran.

Vibrations and Phase Stability in Mixed Valence Antimony Oxide.

α-Sb2O4 (cervantite) and β-Sb2O4 (clinocervantite) are mixed valence compounds with equal proportions of SbIII and SbV as represented in the formula SbIIISbVO4. Their structure and properties can be difficult to calculate owing to the SbIII lone-pair electrons. Here, we present a study of the lattice dynamics and vibrational properties using a combination of inelastic neutron scattering, Mössbauer spectroscopy, nuclear inelastic scattering, and density functional theory (DFT) calculations. DFT calculations that account for lone-pair electrons match the experimental densities of phonon states. Mössbauer spectroscopy reveals the β phase to be significantly harder than the α phase. Calculations with O vacancies reveal the possibility for nonstoichiometric proportions of SbIII and SbV in both phases. An open question is what drives the stability of the α phase over the β phase, as the latter shows pronounced kinetic stability and lower symmetry despite being in the high-temperature phase. Since the vibrational entropy difference is small, it is unlikely to stabilize the α phase. Our results suggest that the α phase is more stable only because the material is not fully stoichiometric.

Growth response of corn due to application of simple mixed compound fertilizer derived from urea - azolla (azolla sp.) - coal fly ash

Mixing urea with natural materials that can reduce the rate of urea dissolution is known to increase the N availability replenished by inorganic fertilizers which absorbed by plants for growth and production.This study aimed to examine the effective of application of pellet N fertilizer prepared by coal fly ash- azolla and urea on the response of corn planted in acidic Ultisol. This pot experiment was performed in the greenhouse and soil analysis was conducted in the Laboratory of Chemistry, Biology and Soil Fertility, Soil Science Department, Faculty of Agriculture, Sriwijaya University. The research was arranged using a completely randomized design with nine treatments and three replications. The treatments applied were a mixed composition materials (w/w) of 50% coal fly ash + 50% azolla, and 40% coal fly ash + 60% azolla respectively. Each composition (w/w) of 70% coal fly ash- Azolla mixture was then incorporated by 30% urea and compacted as pellets using a manual screw extruder. In addition, to compare the effect of pellet, it was done the other treatment by granular urea fertilizer only applied by immersing and sowing on the soil surface. The results showed that the application of N slow release using the pellet forms significantly increased N availability, plant N uptake, plant height and dry weight of corn. The N slow release as a pellet can reduce the dose of N inorganic fertilizer as urea by 25%. The response of corn at a dose of 0.75 times is not significantly different from the dose of 1 times the recommended dose of N.

Kalimat Majemuk dalam Novel Cahaya di Bawah Cahaya Karya Helvy Tiana Rosa, Benny Arnas, dan Asma Nadia

This study discusses how to use compound sentences in the novel “Cahaya di Bawah Cahaya” by Helvy Tiana Rosa, Benny Arnas, and Asma Nadia. The purpose of this research is to describe the use of compound sentences in the novel. The method used in this research is descriptive qualitative method. The data source for this research is the novel “Cahaya di Bawah Cahaya” by Helvy Tiana Rosa, Benny Arnas, and Asma Nadia. Based on the results of data analysis found (1) equivalent compound sentences 64, (2) multilevel compound sentences 21, and (3) mixed compound 32.

Crystal structure, thermal behavior and electric properties of a new semiconductor cobalt-based hybrid material

The crystals of the new organic-inorganic hybrid material, (C5H12N)2[CoBr2.73Cl1.27], were successfully synthesized by the slow evaporation method and characterized by single-crystal X-ray diffraction, thermal analysis, UV–Vis absorption and electrical measurements. This compound crystallizes in the centrosymmetric space group P21/n of the monoclinic system with unit cell parameters: a = 9.7724 (6) Å, b = 12.3920 (6) Å, c = 15.0307 (9) Å, β = 100.864(6) °, V = 1787.59(18) Å3 and Z = 4. The IR spectrum of the compound is studied, especially for the cationic vibrational part. The thermal analysis indicates that (C5H12N)2[CoBr2.73Cl1.27] is stable up to 270 °C and that it undergoes two reversible phase transitions at 152 and 187 °C and at 141 and 128 °C on heating and cooling, respectively. From UV visible gap energy value of 3 eV it can be concluded that the new mixed halide compound is a semiconductor material. The electrical behavior of (C5H12N)2[CoBr2.73Cl1.27] was studied using impedance spectroscopy in the temperature range of 323 to 403 K. According to a study on the frequency dependence of ac conductivity, the material follows Jonscher's universal dynamic law with an increase in the frequency exponent (s) as temperature increases. This behavior reveals that the conduction mechanism is the nonoverlapping small polaron tunneling (NSPT) model.

High temperature oxides for selective absorption of thermal radiation

Most high melting temperature oxides are translucent in the visible-infrared region characteristic of the blackbody thermal radiation at high temperatures. Consequently, over this broad-band spectral region, the “thermal radiation window”, they do not absorb thermal radiation. Translucent oxides, such as the zirconates, can be extensively doped with rare-earth (RE) ions (Nd, Sm, Er, Dy, Yb) to achieve selective spectral absorption, and the doped oxides exhibit low thermal conductivity. The optical absorption bands are due to electronic transitions between electronic states associated with the rare-earth ions and are relatively insensitive to other rare-earth ions within the same compound. Therefore, mixed rare-earth compounds exhibit optical absorption characteristic of the sum of the individual ions’ absorptions. By contrast, the thermal conductivity of the RE zirconates is shown to be relatively independent of composition suggesting that their optical properties in the thermal radiation window regions can be modified without affecting their thermal conduction properties.

The Role of Functional Groups in Tuning the Self-Assembly Modes and Physical Properties of Multicomponent Gels.

We have analyzed the nature and role of functional groups on the self-assembly modes and the physical properties of multicomponent gels with structurally similar individual components. The gelation properties of individual and mixed enantiomeric compounds of biphenyl bis-(amides) of alanine (BPA) or phenylalanine (BPP) methyl ester were analyzed in various solvent/solvent mixtures. Multicomponent gels were formed by mixing the enantiomeric BPP compounds at a lower concentration, but a higher concentration was required for mixed alanine-based BPA gels. The comparison of the mechanical strength of the individual and mixed BPP compounds indicated that the mixed BPP gels displayed enhanced mechanical strength (~2-fold increase) in p-xylene, but a weaker gel was observed in DMSO/water. However, a reverse trend was observed for BPA gels, indicating the role of functional groups in the gel network formation. X-ray diffraction analysis of the gelator and the xerogels in the solid state confirmed the formation of co-assembled networks in mixed enantiomeric gels. The stability of the gels towards anions was evaluated by analyzing the anion induced stimuli-responsive properties. These results indicate the effective modeling of the functional groups of the individual components could lead to multicomponent gels with tunable properties.

Underpinning the ecological response of mixed chlorinated volatile organic compounds (CVOCs) associated with contaminated and bioremediated groundwaters: A potential nexus of microbial community structure and function for strategizing efficient bioremediation

Understanding the structure, dynamics, and functionality of microbial communities is essential for developing sustainable and effective bioremediation strategies, particularly for sites contaminated with mixed chlorinated volatile organic compounds (CVOCs), which can make the biodegradation process more complex and challenging. In this study, 16S rRNA amplicon sequencing revealed a significant change in microbial distribution in response to CVOCs contamination. The loss of sensitive taxa such as Proteobacteria and Acidobacteriota was observed, while CVOCs-resistant taxa such as Campilobacterota were found significantly enriched in contaminated sites. Additionally, varying abundances of crucial enzymes involved in the sequential biodegradation of CVOCs were expressed depending on the contamination level. Association analysis revealed that specific genera such as Sulfurospirillum, Azospira, Trichlorobacter, Acidiphilium, and Magnetospririllum could relatively survive under higher levels of CVOC contamination, whereas pH, ORP and temperature had a negative influence in their abundance and distribution. However, Dechloromonas, Thiobacillus, Pseudarcicella, Hydrogenophaga, and Sulfuritalea showed a negative relationship with CVOC contamination, highlighting their sensitivity towards CVOC contamination. These findings provide valuable insights into the relationship among ecological responses, the groundwater bacterial community, and their functionality in response to mixed CVOC contamination, offering a fundamental basis for developing effective and sustainable bioremediation strategies for CVOC-contaminated groundwater systems.

Perspective on Iron-Based Phosphate Cathode for Commercial Sodium-Ion Cells.

Sodium (Na)-ion batteries (SIBs) have been considered as a potential device for large-scale energy storage. To date, some start-up companies have released their first-generation SIBs cathode materials. Among them, phosphate compounds, particularly iron (Fe)-based mixed phosphate compounds, present great potential for commercial SIBs owing to its low cost, environment friendly. In this perspective, a brief historical retrospect is first introduce to the development of Fe-based mixed phosphate cathodes in SIBs. Then, the recent development about this kind of cathode has been summarized. One of the iron-based phosphate materials, Na3 Fe2 (PO4 )P2 O7 , is used as an example to roughly calculate the energy density and estimate the cost at the cell level to highlight their advantages. Finally, some strategies are put up to further increase the energy density of SIBs. This timely perspective aims to educate the community on the critical benefits of the Fe-based mixed phosphate cathode and provide an up-to-date overview of this emerging field.

Investigation of the stability of organic-inorganic halide perovskite thin films: Insight from experimental and simulation

Herein, we investigated the stability of lead halide perovskites under ambient conditions after mixing the two cations Formamidinium (FA) and Cesium (Cs). The CsxFA1-xPbI3 perovskites solutions were prepared with different contents of x (0.0, 0.3, 0.5, 0.7 and 1.0) and deposited on substrates by spin-coating technique. The CsxFA1-xPbI3 films were, afterwards, characterized using the X-ray diffraction (XRD), UV–visible spectroscopy, photoluminescence (PL) spectra and scanning electron microscopy (SEM) to figure out their crystallinity, morphology, and optical properties. We noticed a stable perovskite structure for the mixed compounds unalike the pure FA and Cs films. The XRD analysis revealed, even after two weeks, the growth and good stability after two weeks of the desired black cubic α-phase perovskite structure in opposite to FAPbI3 and CsPbI3 which, respectively, showed faster degradation and transition into non-perovskite δ-phase and ɣ-phase no perovskite phases. The mixed perovskites Cs-FA also displayed a high absorbance especially for the ones with 30% of Cs and 70% of FA or 50% of each, with an excellent band gap energy ranging between 1.52 and 1.7 eV where FAPbI3 and CsPbI3 were showing a bandgap between 1.5 and 1.9 eV respectively. Moreover, the performance of the CsxFA1-xPbI3 based solar cells were simulated with SCAPS by using the band gaps obtained from the experimental study and after by varying the band gap, the thickness of the absorber layers and then different types of Electron Transport Layer (ETL). The simulation results revealed that the Cs0.3FA0.7PbI3 based solar cells had the highest higher efficiency around 22.36%.

Studies on hydrometallurgical recovery of rare earth elements as mixed fluoride compound from coal fly ash using environmentally friendly organic acid

ABSTRACT Coal fly ash (CFA) emerged as one of the potential secondary source of rare earth elements (REEs). This paper discusses development of a process scheme for the recovery of REE from a CFA sample, assaying total REE of about 0.2% using environmentally benign lactic acid (LA) as leachant. The CFA is generated at a lignite coal-based thermal power plant. The REE occurs dominantly in an ion-exchangeable form and also as bound to iron oxides. Nearly 25% of total REE is constituted of heavy rare earth elements (HREEs). About 89% of REE values were found leachable with LA at 80°C in 2 h of reaction time at 10% solids content. Kinetic analysis of leaching process shows that the reaction between CFA and LA is chemical reaction controlled with activation energy of 42–45 kJ/mol. The dissolved REE values were extracted quantitatively from leachate using D2EHPA solvent diluted in kerosene and stripped back with 6 N HCl. The REE in strip liquor was precipitated as mixed REE-fluoride concentrate of purity 86% with precipitation efficiency of 98%. A scheme for quantitative recovery of LA from barren stream was developed for its recycle in leaching circuit.

Use of Highly Dispersed Mixed Metal Hydroxide Gel Compared to Bentonite Based Gel for Application in Drilling Fluid under Ultra-High Temperatures.

In order to solve the problem of poor dispersion and stability of mixed metal hydroxide (MMH), a kind of mixed metal hydroxide-like compound (MMHlc) gel was synthesized for use as the base mud in drilling fluid instead of bentonite gel. Na2CO3, Na2SiO3, and C17H33CO2Na were used as precipitants to form MMHlc with larger interlayer spacing and smaller particle size. MMHlc was synthesized by the coprecipitation method at 25 °C with a metal molar ratio of Mg:Al:Fe = 3:1:1. The performance evaluation of the treated drilling fluid showed that MMHlc (S2) synthesized using Na2SiO3 as the precipitant had the characteristics of low viscosity, low filtration, and a high dynamic plastic ratio at 25 °C, which fully met the requirements of oil field application, and it maintained its excellent properties after being aged at 250 °C for 16 h. Linear expansion and rolling recovery experiments showed that the S2 sample had excellent rheological properties and good inhibition. X-ray diffraction and FT-IR experiments showed that S2 had the most complete crystal structure, its interlayer distance was large, and its ion exchange capacity was strong. The thermogravimetric experiment showed that the S2 crystal was stable and the temperature resistance of the crystal could reach 340 °C. Zeta potential, particle size analysis, SEM, and TEM results showed that S2 is a nanomaterial with a complete morphology and uniform distribution. The drilling fluid of this formula had the characteristics of low viscosity, low filtration loss, and a high dynamic plastic ratio, and it met the conditions for oil field application. Considering these results, the new MMH prepared by our research institute is a drilling fluid material that can be used at ultra-high temperatures and can provide important support for drilling ultra-deep wells.