Hybrid intercalated duct lesion of the parotid:A case report

BACKGROUND Intercalated duct lesions(IDLs)are considered relatively benign and rare tumors of salivary glands,that were only described recently.Their histopathological appearance may range from ductal hyperplasia to encapsulated adenoma with hybrid patterns of both variants.It is thought that IDLs may be the precursor for malignant proliferations,therefore their correct diagnosis remains crucial for proper lesion management.It is the first reported IDL case arising from the accessory parotid gland(APG),which stands for less frequent but higher malignancy rate tumor developmental area.CASE SUMMARY A 24-years-old male with no accompanying diseases was referred to the hospital with a painless nodule on the right cheek.On physical examination,the stiff,immobile,and painless mass was palpable in the anterior portion of the right parotideomasseteric region,just superior to the parotid duct.Ultrasound examination demonstrated 1.5 cm×1.0 cm hypoechogenic mass on the anterior part of the right parotid gland.Ultrasound-guided fine needle aspiration cytology,followed by liquid-based fine needle aspiration biopsy were performed.However,the results were uninformative.A contrast-enhanced magnetic res-onance imaging(MRI)of the parotid was obtained,demonstrating a 1.5 cm×1.0 cm×0.5 cm tumor with high intensity capsule together with low intensity core in the very anterior part of right superficial lobe,situated in the APG.An MRI features were uncharacteristic to common parotid tumors,therefore surgical resection followed up.After histopathological examination,the final diagnosis of hybrid IDL was confirmed.CONCLUSION Fine needle aspiration biopsy might not always be diagnostic,and given the malignant potential,the surgical resection of such lesion remains the treatment of choice.

Structural engineering of potassium vanadate cathode by pre-intercalated Mg_(2+) for high-performance and durable rechargeable aqueous zinc-ion batteries

Aqueous zinc(Zn)-ion batteries(AZIBs)have the potential to be used in massive energy storage owing to their low cost,eco-friendliness,safety,and good energy density.Significant research has been focused on enhancing the performance of AZIBs,but challenges persist.Vanadium-based oxides,known for their large interlayer spacing,are promising cathode materials.In this report,we synthesize Mg^(2+)-intercalated potassium vanadate(KVO)(MgKVO)via a single-step hydrothermal method and achieve a 12.2°Ainterlayer spacing.Mg^(2+) intercalation enhances the KVO performance,providing wide channels for Zn^(2+),which results in high capacity and ion diffusion.The combined action of K^(+) and Mg^(2+) intercalation enhances the electrical conductivity of MgKVO.This structural design endows MgKVO with excellent electrochemical performance.The AZIB with the MgKVO cathode delivers a high capacity of 457 mAh g^(-1) at 0.5 A g^(-1),excellent rate performance of 298 mAh g^(-1) at 5 A g^(-1),and outstanding cycling stability of 102%over 1300 cycles at 3 A g^(-1).Additionally,pseudocapacitance analysis reveals the high capacitance contribution and Zn^(2+)diffusion coefficient of MgKVO.Notably,ex-situ X-ray diffraction,X-ray photoelectron spectroscopy,and Raman analyses further demonstrate the Zn^(2+)insertion/extraction and Zn-ion storage mechanisms that occurred during cycling in the battery system.This study provides new insights into the intercalation of dual cations in vanadium oxides and offers new solutions for designing cathodes for high-capacity AZIBs.

Intercalation Assembly Method and Intercalation Process Control of Layered Intercalated Functional Materials

Layered intercalated functional materials of layered double hydroxide type are an important class of functional materials developed in recent years. Based on long term studies on these materials in the State Key Laboratory of Chemical Resource Engineering in Beiiing University of Chemical Technology, the orinciole for the design of controlled intercalation processes in the light of tuture production processing requirements has been developed. Intercalation assembly methods and technologies have been invented to control the intercalation process for preparing layered intercalated materials with various structures and functions.

Metallic vanadium trioxide intercalated with phase transformation for advanced aqueous zinc-ion batteries

Aqueous zinc-ion batteries have broad application prospects due to the eco-friendliness,cost-economy and high safety.However,the scarcity of high-performance cathodes with outstanding rate capability and long lifespan has affected their development.Herein,we report a metallic vanadium trioxide material intercalated with phase transformation as cathode applied in aqueous zinc-ion batteries.It offers satisfactory electrochemical performances with a high specific capacity(435 mAh g^(-1) at 0.5 A g^(-1)),decent power density(5.23 kW kg^(-1))and desired energy density(331 Wh kg^(-1)),as well as good cyclability.The superior performance originates from the stable structure and fast Zn^(2+)diffusion,enabled by the pre-intercalation of Zn^(2+)and water molecules.

Numerical analysis of loess and weak intercalated layer failure behavior under direct shearing and cyclic loading

The mechanical behavior of the joints inside a loess layer is greatly important in weak intercalation studies owing to its involvement in a wide range of landslides in the loess region in China.The shear behavior of the joints in the loess stratum during direct shear and cyclic loadings was investigated using the PFC2D discrete element software.Loess mudstone and mudstone with weak intercalated layer materials were subjected to direct testing,and cyclic shear tests were conducted with consideration to the influence of normal stress and shear velocity.The macroscopic properties and damage patterns were obtained for six numerical configurations;namely,loess-weathered mudstone with 0°,10°,and-10°joints and weathered mudstone with 0°,10°,and-10°weak intercalated layers.The numerical test results revealed that,in the direct shear tests,the shear stress and shear displacement of the samples increased with the normal stress.In the cyclic shear tests with a total cycle number N=20,the shear stress-shear strain curve of the six different configurations exhibited a hysteresis loop.The numerical tests also revealed that,under cyclic shear,the normal stress and shear velocity affected the shear strength.The degree of damage increased as the shear velocity decreased from 0.1 mm/s to 0.005 mm/s for all six numerical configurations.Compared with the damage pattern of the direct shear tests,the damage of the cyclic shear tests mainly comprised shear cracks and fractures,some shaking consolidation settlement and fewer shear strain occurred around the joints.In the direct shear tests,more compression cracks and fractures occurred in the samples.The damage mainly developed along the joints,and shearing-off damage occurred.The results obtained by this study further elucidate the failure mechanism and microscopic damage response of the joints in the loess stratum in Northwest China.

Adsorption of CO_(2) on MgAl layered double hydroxides: Effect of intercalated anion and alkaline etching time

The adsorption of CO_(2) on MgAl layered double hydroxides(MgAl-LDHs) based adsorbents has been an effective way to capture CO_(2),however the adsorption capacity was hampered due to the pore structure and the dispersibility of adsorption active sites.To address the problem,we investigate the effect of intercalated anion and alkaline etching time on the structure,morphology and CO_(2) uptake performances of MgAl-LDHs.MgAl-LDHs are synthesized by the onepot hydrothermal method,followed by alkaline etching of NaOH,and characterized by x-ray diffraction,N_(2) adsorption,scanning electron microscopy and Fourier transform infrared spectroscopy.The CO_(2) adsorption tests of the samples are performed on a thermogravimetric analyzer,and the adsorption data are fitted by the first-order,pseudo-second-order and Elovich models,respectively.The results demonstrate that among the three intercalated samples,MgAl(Cl) using chloride salts as precursors possesses the highest adsorption capacity of CO_(2),owing to high crystallinity and porous structure,while MgAl(Ac) employing acetate salts as precursors displays the lowest CO_(2) uptake because of poor crystallinity,disorderly stacked structure and unsatisfactory pore structure.With regard to alkaline etching,the surface of the treated MgAl(Cl) is partly corroded,thus the specific surface area and pore volume increase,which is conducive to the exposure of adsorption active sites.Correspondingly,the adsorption performance of the alkaline-etched adsorbents is significantly improved,and MgAl(Cl)-6 has the highest CO_(2) uptake.With the alkaline etching time further increasing,the CO_(2) adsorption capacity of MgAl(Cl)-9 sharply decreases,mainly due to the collapse of pore structure and the fragmentized sheet-structure.Hence,the CO_(2) adsorption performance is greatly influenced by alkaline etching time,and appropriate alkaline etching time can facilitate the contact between CO_(2) molecules and the adsorbent.

Composites on Base of the Ultradispersed Polytetrafluoroethylene and Graphite Oxide Intercalated Compounds

Composites based on ultradispersed polytetrafluoroethylene and intercalated graphite oxide compounds with dodecahydro-closo-dodecaborates and methods of their fabrication have been developed. The fabricated composites have been characterized using XRD analysis, and optical microscopy. These composites are distinguished with completeness of their combustion, since the combustion products comprise gaseous boron fluorine-containing compounds of boron, boron trifluoride (BF3), and boron oxyfluoride ((BOF)3). Besides, these composites are characterized with increased energy capacity as compared to purely oxygen-containing compounds, since the heat of formation of boron fluorine-containing compounds is higher than that of boron oxide. Introduction of ultradispersed polytetrafluoroethylene imparts composites with hydrophobicity, thus improving their functioning properties.

Unsaturated Creep Behaviors of Weak Intercalated Soils in Soft Rock of Badong Formation

The cutting slopes in soft rock of redbed appeared in Yichang-Badong highway often suffer from the instability along weak intercalations, so the creep behaviors of weak intercalated soils are crucially important for the stability of cutting slopes. Because the deformation of weak intercalated soils is significantly affected by water content due to the strong water sensitivity, it is necessary to study the influence of matric suction on the creep behaviors of weak intercalated soils. In order to find out the unsaturated creep characters of weak intercalated soils, a GDS unsaturated triaxial apparatus was used. Then the triaxial creep experiments on weak intercalated soil samples under varying matric suction were conducted to obtain the unsaturated creep curves. The results show that the weak intercalated soils have obvious creep behaviors, and the creep strain is in nonlinear relationship with stress and time. When the matric suction is constant, a larger deviator stress will lead to a larger creep strain; When the deviator stress is constant, a smaller matric suction will lead to a larger creep strain. Based on the Mesri creep model, an improved creep model for weak intercalated soils under varying matric suction was established, in which the relationship of stress-strain was expressed with a hyperbolic function, and the relationship of strain-time was expressed with power functions in stages. Then an unsaturated creep model including stress-matric suction-strain-time for weak intercalated soils was established based on the power function relationship between matric suction and Ed(a parameter of the improved creep model). The comparison of the calculated values of creep model and the experimental values shows that the creep behaviors of weak intercalated soils can be predicted by the unsaturated creep model by and large.

EFFECT OF AMPHIPHILIC POLY (STYRENE-B-ETHYLENE OXIDE) DIBLOCK COPOLYMER INTERCALATED LAYERED SILICATE AS FILLER ON ACRYLONITRILE-BUTADIENE-STYRENE RESIN

The diblock copolymers intercalated layered silicate was prepared via a melt dispersion technique. Then the effect of intercalated hybrid as filler on acrylonitrile- butadiene-styrene resin was characterized by X-ray diffraction, transmission electron microscopy, stress-strain measurements in elongation.

Intercalation Assembly and Chemical Product Engineering of Layered Intercalated Functional Materials Based on Efficient Utilization of Magnesium Resources in Salt Lakes

1 Introduction Magnesium salts are very important by-product of salt lake industry in West China.Nearly 200 million cubic meters of waste brine are released to the environment

OPTIMIZATION OF THE METHOD OF SELECTING THE TOOTH NUMBER SERIES IN A SET OF CHANGE GEARS Part Ⅱ The Rules for Permuting the DBL’s of the First Order and Their Intercalated Sets

The problem in practice of determining the proper combination of Zi in a set of changegears may be abstracted to the problem of finding the proper combination and permutation ofthe elements ai,i+1 of the set A1 to give maximum M-d. Some results to find optimal combina-tions of the elements of the set A1 have been reported in part I. In this part, some rules forpermuting these elements are introduced. By means of these rules, three kinds of intercalated setsof A1 have been found, namely: （1） Sets with an even left wing, （2） Sets with coincidence of bothwings, and （3） Sets with circulated elements.

Synergistically coupling of graphene quantum dots with Zn-intercalated MnO2 cathode for high-performance aqueous Zn-ion batteries

Cost-effective,safe,and highly performing energy storage devices require rechargeable batteries,and among various options,aqueous zinc-ion batteries(ZIBs)have shown high promise in this regard.As a cathode material for the aqueous ZIBs,manganese dioxide(MnO_(2))has been found to be promising,but certain drawbacks of this cathode material are slow charge-transfer capability and poor cycling performance.Herein,a novel design of graphene quantum dots(GQDs)integrated with Zn-intercalated MnO_(2)nanosheets is put forward to construct a 3D nanoflower-like GQDs@ZnxMnO_(2)composite cathode for aqueous ZIBs.The synergistic coupling of GQDs modification with Zn intercalation provides abundant active sites and conductive medium to facilitate the ion/electron transmission,as well as ensure the GQDs@ZnxMnO_(2)composite cathode with enhanced charge-transfer capability and high electrochemical reversibility,which are elucidated by experiment results and in-situ Raman investigation.These impressive properties endow the GQDs@ZnxMnO_(2)composite cathode with superior aqueous Zn^(2+) storage capacity(~403.6 mAh·g^(−1)),excellent electrochemical kinetics,and good structural stability.For actual applications,the fabricated aqueous ZIBs can deliver a substantial energy density(226.8 W·h·kg^(−1)),a remarkable power density(650 W·kg^(−1)),and long-term cycle performance,further stimulating their potential application as efficient electrochemical storage devices for various energy-related fields.

Work function tuned, surface Cs intercalated BiVO_(4) for enhanced photoelectrochemical water splitting reactions

Monoclinic BiVO_(4) is a widely researched semiconductor in solar water splitting owing to its suitable characteristics. However, BiVO_(4) faces limitations, such as the inefficient separation and transportation of photogenerated charges in the bulk and poor catalytic water oxidation reactions at the surface that affect the water-splitting efficiency. In this work, the Cs intercalation strategy at the surface of BiVO_(4) is proposed for the enhanced water splitting to H_(2) and O_(2) productions via the effective separation and transportation photogenerated charges and improved surface catalytic water oxidation reactions. The Cs ions are found to intercalate at the surface of BiVO_(4) and regulate the oxygen vacancies to provide active O_(2) production sites and stability. The surface intercalation of Cs boosts the photocurrent to 1.89 mA cm^(-2)at 1.23 V vs.reference hydrogen electrode(RHE). A stoichiometric evolution of H_(2) and O_(2) is recorded with a faradaic efficiency of 92%. The open-circuit voltage measurements confirmed the increase in the carrier lifetime with the work function tuning upon Cs intercalation. The proposed Cs intercalation strategy suggests an effective route to suppress the charge recombination with an increase in carrier lifetime and charge separation in BiVO_(4) for the enhanced PEC application.

Electrochemically triggered decoupled transport behaviors in intercalated graphite:From energy storage to enhanced electromagnetic applications

Pyrolytic graphite (PG) with highly aligned graphene layers,present anisotropic electrical and thermal transport behavior,which is attractive in electronic,electrocatalyst and energy storage.Such pristine PG could meeting the limit of electrical conductivity (~2.5×10^(4) S·cm^(−1)),although efforts have been made for achieving high-purity sp^(2) hybridized carbon.For manipulating the electrical conductivity of PG,a facile and efficient electrochemical strategy is demonstrated to enhance electrical transport ability via reversible intercalation/de-intercalation of AlCl_(4)^(-)into the graphitic interlayers.With the stage evolution at different voltages,variable electrical and thermal transport behaviors could be achieved via controlling AlCl_(4)^(-)concentrations in the PG because of substantial variation in the electronic density of states.Such evolution leads to decoupled electrical and thermal transport (opposite variation trend) in the in-plane and out-of-plane directions,and the in-plane electrical conductivity of the pristine PG (1.25×10^(4) S·cm^(−1)) could be massively promoted to 4.09×10^(4) S·cm(AlCl_(4)^(-)intercalated PG),much better than the pristine bulk graphitic papers used for the electrical transport and electromagnetic shielding.The fundamental mechanism of decoupled transport feature and electrochemical strategy here could be extended into other anisotropic conductive bulks for achieving unusual behaviors.

Metal porphyrin intercalated reduced graphene oxide nanocomposite utilized for electrocatalytic oxygen reduction

In this paper, we report a simple and facile self-assembly method to successfully fabricate cationic metal porphyrin-MtTMPyP(Mt= Cobalt(Ⅱ), Manganese(Ⅲ), or Iron(Ⅲ); TMPyP = 5, 10, 15, 20-tetrakis(N-methylpyridinium-4-yl) porphyrin) intercalated into the layer of graphene oxide(GO) by the cooperative effects of electrostatic and π-π stacking interaction between positively charged metal porphyrin and negatively charged GO sheets. Followed by reduction with hydrazine vapor, a series of novel 2 D MtTMPyP/rGO_n were fabricated. The as-prepared 2 D hybrids were fully characterized and tested as non-noble metal catalysts for oxygen reduction reaction(ORR) in an alkaline medium. The MtTMPyP/rGO_n hybrids, especially CoTMPyP/rGO_5, demonstrated an improved electrocatalytic activity for ORR and a number of exchanged electrons close to 4-electron reaction, increased stability and excellent tolerance to methanol, showing a potential alternative catalyst for ORR in fuel cells and air batteries.

Intercalated water in aqueous batteries

The unprecedentedly growing demand for energy storage devices in recent years calls for diversified chemistries with unique advantages.When it comes to safety and cost,aqueous battery systems have attracted tremendous attention.Owing to its small size,high polarity,and hydrogen bonding,water in the electrode materials,either in the form of structural water or cointercalated hydrated cations,drastically change the electrochemical behavior through multiple aspects.This review discusses the roles of water in aqueous batteries from how water molecules coordinate with cations to examples of watermediated reactions in different types of host materials.

Interlayer environment engineered MXene: Pre-intercalated Zn^(2+)ions as intercalants renders the modulated Li storage

The intercalation of foreign species into MXene, as an approach of tuning the interlayer environment, is employed to improve electrochemical ion storage behaviors. Herein, to understand the effect of confined ions by the MXene layers on the performance of electrochemical energy storage, Zn^(2+) ions were employed to intercalate into MXene via an electrochemical technique. Zn^(2+) ions induced a shrink of the adjacent MXene layers. Meaningfully, a higher capacity of lithium ion storage was obtained after Zn^(2+) preintercalation. In order to explore the roles of the intercalated Zn^(2+) ions, the structural evolution, and the electronic migration among Zn, Ti and the surface termination were investigated to trace the origination of the higher Li^(+) storage capacity. The pre-intercalated Zn^(2+) ions lost electrons, meanwhile Ti of MXene obtained electrons. Moreover, a low-F surface functional groups was achieved. Contrary to the first shrink, after 200 cycles, a larger interlayer distance was monitored, this can accelerate the ion transport and offer a larger expansile space for lithium storage. This may offer a guidance to understand the roles of the confined ion by two-dimensional(2D) layered materials.

Curie and Pauli Spins in Lithium Intercalated MCMB

The ESR signal of lithium intercalated MCMB can be well simulated by combination of a Lorentz curve and a Gauss curve. The ESR intensity of the Lorentz component is essentially independent of temperature while the Gauss component shows a linear change with the reciprocal of temperature, indicative of Pauli spin and Curie spin, respectively. The former is probably associated with the ordered (graphitized) structures while the latter with the disordered structures in the sample.

Characterizing silicon intercalated graphene grown epitaxially on Ir films by atomic force microscopy

An efficient method based on atomic force microscopy（AFM） has been developed to characterize silicon intercalated graphene grown on single crystalline Ir（111） thin films. By combining analyses of the phase image, force curves,and friction–force mapping, acquired by AFM, the locations and coverages of graphene and silicon oxide can be well distinguished. We can also demonstrate that silicon atoms have been successfully intercalated between graphene and the substrate. Our method gives an efficient and simple way to characterize graphene samples with interacted atoms and is very helpful for future applications of graphene-based devices in the modern microelectronic industry, where AFM is already widely used.

Electrochemical synthesis of alkali-intercalated iron selenide superconductors

Electrochemical method has been used to insert K/Na into FeSe lattice to prepare alkali-intercalated iron selenides at room temperature. Magnetization measurement reveals that KxFe2Se2 and NaxFe2Se2 are superconductive at 31 K and 46 K, respectively. This is the first successful report of obtaining metal-intercalated FeSe-based high-temperature superconductors using electrochemical method. It provides an effective route to synthesize metal-intercalated layered compounds for new superconductor exploration.