Efficient lubrication of magnesium alloys is a highly challenging topic in the field of tribology.In this study,magnesium silicate hydroxide(MSH)nanotubes with serpentine structures were synthesized.The tribological b...Efficient lubrication of magnesium alloys is a highly challenging topic in the field of tribology.In this study,magnesium silicate hydroxide(MSH)nanotubes with serpentine structures were synthesized.The tribological behavior of AZ91D magnesium alloy rubbed against GCr15 steel was studied under lubricating oil with surface-modified MSH nanotubes as additives.The effects of the concentration,applied load,and reciprocating frequency on the friction and wear of the AZ91D alloy were studied using an SRV-4 sliding wear tester.Results show a decrease of 18.7–68.5%in friction coefficient,and a reduction of 19.4–54.3%in wear volume of magnesium alloy can be achieved by applying the synthetic serpentine additive under different conditions.A suspension containing 0.3 wt.%MSH was most efficient in reducing wear and friction.High frequency and medium load were more conducive to improving the tribological properties of magnesium alloys.A series of beneficial physical and chemical processes occurring at the AZ91D alloy/steel interface can be used to explain friction and wear reduction based on the characterization of the morphology,chemical composition,chemical state,microstructure,and nanomechanical properties of the worn surface.The synthetic MSH,with serpentine structure and nanotube morphology,possesses excellent adsorbability,high chemical activity,and good self-lubrication and catalytic activity.Therefore,physical polishing,tribochemical reactions,and physicalchemical depositions can occur easily on the sliding contacts.A dense tribolayer with a complex composition and composite structure was formed on the worn surface.Its high hardness,good toughness and plasticity,and prominent lubricity resulted in the improvement of friction and wear,making the synthetic MSH a promising efficient oil additive for magnesium alloys under boundary and mixed lubrication.展开更多
Aqueous zinc-based energy storage systems offer high theoretical specific capacity,low cost,intrinsic safety,and environmental compatibility,positioning them as promising candidates for next-generation energy storage ...Aqueous zinc-based energy storage systems offer high theoretical specific capacity,low cost,intrinsic safety,and environmental compatibility,positioning them as promising candidates for next-generation energy storage and conversion technologies.However,issues such as zinc dendrite growth,hydrogen evolution reaction(HER),and surface passivation hinder their practical deployment.To address these challenges,a hollow nanotubular magnesium silicate(denoted MgSi)interfacial layer was constructed on the zinc metal anode(Zn@MgSi).The unique layer structure and negatively charged surface of MgSi facilitate the desolvation of[Zn(H_(2)O)_(6)]^(2+)by stripping water molecules,while temporarily immobilizing Zn^(2+)to suppress random diffusion.The combined effects of the electric field-guided Zn^(2+)distribution and rapid ion transport through the layer structure co-regulate Zn^(2+)flux,leading to uniform,dendrite-free zinc deposition.Consequently,the Zn@MgSi symmetric cell demonstrates a high Zn^(2+)transference number(0.64),extended cycling life exceeding 1600 h at 1 mA cm^(−2),and stable operation for 200 h at 5 mA cm^(−2).Furthermore,zinc-ion hybrid capacitors employing Zn@MgSi electrodes exhibit excellent cycling stability over 5000 cycles.This work highlights the efficacy of artificial interfacial layers in stabilizing zinc metal anodes and provides valuable insights into the development of advanced aqueous zinc-ion energy storage systems.展开更多
Batch adsorption from aqueous solutions in a slightly basic medium of Methylene Blue, up to 2500 mg/L, onto synthetic magnesium silicate （Florisil） of three particle size ranges （mean diameters of 112, 200 and 425 ...Batch adsorption from aqueous solutions in a slightly basic medium of Methylene Blue, up to 2500 mg/L, onto synthetic magnesium silicate （Florisil） of three particle size ranges （mean diameters of 112, 200 and 425 μm） was compared to the corresponding adsorption onto activated carbon and Amberlite XAD-2. The best fit of the kinetic results was achieved by a pseudo second-order equation. The equilibrium data were found to be well represented by the Langmuir isotherm equation. Amberlite XAD-2, an unspecific adsorbent capable of adsorbing exclusively through a surface effect, exhibited a poor dye uptake, confirming that the adsorption mechanism on Florisil was due to electrostatic attraction and ion exchange. Moreover, the comparison between Florisil and the other adsorbents was performed on the basis of the evaluation of the surface area and pore volume occupied by the adsorbed dye.展开更多
In order to expand the advantages of strong durability and high compressive strength of calcium silicate hydrates(C-S-H),at the same time to make up for the poor early mechanical strength of magnesium silicate hydrate...In order to expand the advantages of strong durability and high compressive strength of calcium silicate hydrates(C-S-H),at the same time to make up for the poor early mechanical strength of magnesium silicate hydrates (M-S-H),we present the features and advantages of C-S-H and M-S-H and a comprehensive review of the progress on CaO-MgO-SiO_(2)-H_(2)O.Moreover,we systematically describe natural calcium and magnesium silicate minerals and thermodynamic properties of CaO-MgO-SiO_(2)-H_(2)O.The effect of magnesium on C-S-H and calcium on M-S-H is summarized deeply;the formation and structural feature of CaO-MgO-SiO_(2)-H_(2)O is also explained in detail.Finally,the development of calcium and magnesium silicate hydrates in the future is pointed out,and the further research is discussed and estimated.展开更多
Solid-state batteries with solid polymer electrolytes are considered the most promising due to their high energy density and safety advantages.However,their development is hindered by the limitations of polymer electr...Solid-state batteries with solid polymer electrolytes are considered the most promising due to their high energy density and safety advantages.However,their development is hindered by the limitations of polymer electrolytes,such as low ionic conductivity,poor mechanical strength and inadequate fire resistance.This study presents a thin polyvinylidene fluoride-based composite solid electrolyte film(25μm incorporating twodimensional modified lipophilic lithium magnesium silicate(LLS)as additives with good dispersibility.The incorporation of LLS promotes grain refinement in polyvinylidene fluoride(PVDF),enhances the densification of electrolyte films,increases the tensile strength to10.42 MPa and the elongation to 251.58%,improves ion transport interfac e,and facilitates uniform deposition of lithium ions.Furthermore,LLS demonstrates strong adsorption ability,promoting the formation of solvated molecules,resulting in high ionic conductivity(2.07×10^(-4)S·cm^(-1)at 30℃)and a stable lithium/electrolyte interface.Symmetric Li//Li cells assembled with the thin composite electrolytes exhibit stable cycling for2000 h at 0.1 mA·cm^(-2)and 0.05 mAh·cm^(-2).Additionally,the LiFePO_(4)//Li battery shows a capacity retention rate of99.9%after 200 cycles at 0.5C and room temperature.展开更多
This study aims to investigate the behavior of alkali activated mortar,which is made of naturally available magnesium silicate as source material.For magnesium silicate,ultrafine natural steatite powder(UFNSP)is used ...This study aims to investigate the behavior of alkali activated mortar,which is made of naturally available magnesium silicate as source material.For magnesium silicate,ultrafine natural steatite powder(UFNSP)is used as the primary source of binder,and the activation is initiated through the alkali liquid which is proportioned in various combinations of silicate to hydroxide ratio(Na_(2)SiO_(3)/Na OH)ratio,and this ratio in this study varies from 1 to 3.The UFNSP is calcined at two difierent temperatures,700 and 1000℃.The mortar mix is proportioned as 1:3 between powder and the fine aggregate,and the mortar is prepared with hydroxide molarity(M)of 10 M.The mortar is cured for 48 hours at 60℃and the compressive strength was studied.All the mix were studied for its microstructural behavior along with compressive strength.The mix proportion of the mortar,and the results obtained through microstructural characterization were combinedly formed as input for artificial neural network(ANN)predictive modelling.The model is designed to predict the compressive strength,which is trained through Bayesian regularization algorithm with varying hidden neurons of 7 to 10.This experimental and predictive study shows that the strength is influenced by both Na_(2)SiO_(3)/Na OH ratio and calcination process.And the ANN is influenced by mainly calcination temperature and uncorrelation occurs in selected samples of 1000℃calcined UFNSP mix.展开更多
Given the confluence of dysregulated inflammation,vasculopathy,and neuropathy,diabetic wounds pose a significant clinical challenge.Commercially available wound dressings often lack sufficient bioactivity,failing to m...Given the confluence of dysregulated inflammation,vasculopathy,and neuropathy,diabetic wounds pose a significant clinical challenge.Commercially available wound dressings often lack sufficient bioactivity,failing to meet clinical demands.Herein,we developed a PCL-PLLA-MgSiO_(3)(PP-MgSi)patch with promising therapeutic effects.The PP-MgSi composite patch was manufactured via electrospinning and characterized by controllable degradation and local release of Mg^(2+)and SiO_(3)^(2−).The patch showed favorable in vitro biocompatibility and bioactivity,notably increased angiogenesis,myelination,and neurite outgrowth.In type 2 diabetic mice,the PP-MgSi patch exhibited MgSi dose-dependent effects on enhancing diabetic wound healing by modulating the expression of TNF-α,iNOS,and CD206 to balance inflammation,while boosting CD31 andβ3-tubulin levels to promote neurovascularization.With the significant suppression of pro-inflammatory-related TNF and IL-17 pathways,while activating the peripheral nerve-associated axon guidance pathway,blood vessel-associated HIF-1αand VEGF pathways,the PP-MgSi patch ultimately achieved accelerated healing compared to the control group.Ultimately,the PP-MgSi patch exhibited an accelerated repair rate,with comparable neovascularization and superior peripheral nerve regeneration capacity compared to three representative commercially available products.This proof-of-concept work presents a promising bioactive PP-MgSi patch for future clinical diabetic wound management,particularly in terms of its neurovascular network recovery properties.展开更多
Hierarchical porous magnesium silicate hydrate (MSH) microspheres composed of sheets are successfully developed under facile conditions using a hard template. The role of hexadecyltrimethylammonium bromide (CTAB) on t...Hierarchical porous magnesium silicate hydrate (MSH) microspheres composed of sheets are successfully developed under facile conditions using a hard template. The role of hexadecyltrimethylammonium bromide (CTAB) on the formation and adsorption behavior was also observed for the methyl orange and methylene blue. The formed MSH possesses a surface area of 453.24 m^(2)/g, an average pore size of 6.38 nm, and a pore volume of 0.75 cm^(3)/g without CTAB. Based on the role of CTAB and the change in the ratio of Mg/Si, the MSH retained its sphere-like structure with a variation in pore parameters. The formed MSH was used as an adsorbent to remove methylene blue and methyl orange. The pseudo-second-order kinetic and Langmuir Isotherm models are well-fitted, with a 256.4 mg/g removal capacity and 84.2 mg/g for methylene blue and methyl orange, respectively. The modified MSH with CTAB played a positive role for the methyl orange and a negative role for the methylene blue regarding removal performance.展开更多
Airborne silicate pollutants in flight corridors pose a serious threat to aviation safety whose severity is directly linked to the wettability of molten silicates on thermal barrier coatings(TBCs)at high temperatures(...Airborne silicate pollutants in flight corridors pose a serious threat to aviation safety whose severity is directly linked to the wettability of molten silicates on thermal barrier coatings(TBCs)at high temperatures(1200–2000℃).Despite its importance,the wettability of silicate melt on TBCs has not been well investigated.In particular,the surface morphology characteristics of TBCs can be expected to have a first-order effect on the wettability of silicate melt on such TBCs.Here,a series of atmospheric plasma spray(APS)yttria-stabilized zirconia(YSZ)TBCs with varying surface roughness were generated through the application of mechanical polishing.The metastable nonwetting behavior of three representative types of airborne silicate ash(volcanic ash,fly ash and a synthetic calcium–magnesium–aluminum–silicates(CMAS)powder)on these TBCs with varying surface roughness was investigated.It was observed that the smoother the surface of TBCs was,the larger the contact angle was with the molten silicate melts,and consequently,the smaller the area of damage was on the TBCs.Thus,the reduction in TBCs surface roughness(here via mechanical polishing)led to an improvement in the wetting and spreading resistance of TBCs to silicate melts at high temperature.In support of these observations and conclusions,the surface morphology of the TBC(both before and after polishing)had been characterized,and the mechanism of the surface roughness-dependence of wettability had been discussed.These results should contribute to reducing the deposition rate of silicate melt on TBCs,thus extending the lifetime of turbine blades and reducing maintenance costs.展开更多
Finding appropriate flotation reagents to separate copper-nickel sulfide ores from various magnesium silicate gangue minerals has always been a challenge in the mineral processing industry.This study introduced xantha...Finding appropriate flotation reagents to separate copper-nickel sulfide ores from various magnesium silicate gangue minerals has always been a challenge in the mineral processing industry.This study introduced xanthan gum(XG)as a non-toxic and environmentally friendly depressant of talc,olivine,and serpentine.The effects and mechanisms of XG on the aggregation and flotation behavior of talc,olivine and serpentine were investigated by flotation tests,sedimentation tests,IC-FBRM particle size analysis tests,adsorption quantity tests,Fourier transform infrared spectroscopy(FTIR)tests,X-ray photoelectron spectroscopy(XPS)analysis tests and Zeta potential tests.The flotation results indicated that when the three minerals were mixed,XG caused the talc-serpentine aggregation in the solution to shift to olivine-serpentine aggregation,with the remaining XG adsorbing on talc to depress its flotation.In addition,combining XPS and zeta potential tests,the-OH(hydroxyl)groups in XG molecules preferentially adsorbed on Mg sites on the surface of olivine through chemical bonding.The surface potential of olivine significantly shifted to a more negative value,with the negative charge on the olivine surface far exceeding that on the talc surface.This resulted in an increased aggregation effect between positively charged serpentine and negatively charged olivine due to enhanced electrostatic forces.展开更多
Long afterglow photoluminescent materials Sr2MgSi2O7 doped with Eu2+, Dy3+ were prepared by sol-gel method. The synthesized samples were characterized by X-ray diffraction. The excitation spectrum, emission spectrum a...Long afterglow photoluminescent materials Sr2MgSi2O7 doped with Eu2+, Dy3+ were prepared by sol-gel method. The synthesized samples were characterized by X-ray diffraction. The excitation spectrum, emission spectrum and long decay curve were measured and analyzed. XRD pattern indicates that phosphor is with Sr2MgSi2O7 crystal structure. The wide range of excitation wavelength indicates that luminescent material can be excited by light from ultraviolet ray to visible light. The main peak of emission spectrum is located at 466 nm. Sample excited by visible light can emit bright blue light, and the afterglow time lasts more than 8 h.展开更多
The paste was prepared by mixing MgO, microsilica and H2O in the presence of water reducer at different reaction ratios and temperatures, and characterized by XRD, DTA, TGA, IR, and solid-state 29Si NMR. The experimen...The paste was prepared by mixing MgO, microsilica and H2O in the presence of water reducer at different reaction ratios and temperatures, and characterized by XRD, DTA, TGA, IR, and solid-state 29Si NMR. The experimental results showed that, besides Mg（OH）2, magnesium silicate hydrate （M-S-H） was formed at a low temperature such as 25 and 50 ℃. At a high temperature of 100 ℃, Mg（OH）2 can be further transformed into M-S-H completely, for instance, within ca. 1 month in an excess of microsilica. The average composition and structure of M-S-H was mainly related to the reaction mixture and curing temperature and was discussed in detail.展开更多
It was proved that MgO and MicroSilica can react at room temperature, giving a hardened product primarily comprised of Mg （ OH ）2 and Magnesium Silicate Hydrate （ M- S- H ）. The reaction ratio and process and the ...It was proved that MgO and MicroSilica can react at room temperature, giving a hardened product primarily comprised of Mg （ OH ）2 and Magnesium Silicate Hydrate （ M- S- H ）. The reaction ratio and process and the chemical composion of M- S- H were studied and analyzed by QXRD and DTA- TG. The experimental results indicate that much Mg（ OH）2 and less M-S-H were formed at early period. After 7 days there is no change in the quantity of Mg（ OH）2, while M-S-H was increased slowly. The chemical composion of M-S-H would vary with the mix proportion in the hydrution process , but M1.32 SH2.37 is finally the approximute form.展开更多
Sol-gel method was utilized to synthesize two different series of red silicate phosphors : MgSiO3 and Mg2SiO4 powder samples doped with Mn2+, conducted the investigation of red long-lasting phosphor: MgSiO3 : Eu2 + , ...Sol-gel method was utilized to synthesize two different series of red silicate phosphors : MgSiO3 and Mg2SiO4 powder samples doped with Mn2+, conducted the investigation of red long-lasting phosphor: MgSiO3 : Eu2 + , Dy3+, Mn2+ . TGA curves of the gel precursor for two series depicted that the loss of residual organic groups and NO3 groups occurs below 450℃. According to the XRD patterns, the major diffraction peaks of the MgSiO3 and Mg2SiO4 series are consistent with a proto-enstatite structure (JCPDS No.11-0273) and a forsterite structure (JCPDS No.85-1364) respectively. With the excitation at 415 nm, the red emission band of Mn2+ ions is peaked at 661 nm for MgSiO3:1%(atom fraction) Mn2+ or 644 nm for MgiSiO4: 1 %(atom fraction) Mn2+ . Compared with Mg2SiO4:Mn2+ samples, MgSiO3:Mn2+ samples exhibit higher luminescence intensity and higher quenching concentration. In addition, the two series co-doped with Eu2+ , Dy3+ , Mn2+ were also prepared. Photo-luminescence and afterglow properties of the two co-doped series were analyzed, which show that MgSiO3: Eu2 + , Dy3+ , Mn2+ is more suitable for a red long-lasting phosphor.展开更多
Crystallization characteristic of periclase in clinker and effect of Mg^2+ on hydrate of cement pastes were investigated. Morphologies and relative content of periclase were characterized with scanning electron micros...Crystallization characteristic of periclase in clinker and effect of Mg^2+ on hydrate of cement pastes were investigated. Morphologies and relative content of periclase were characterized with scanning electron microscopy and X-ray diffraction. Derivative thermogravimetry analysis and backscattered electron imaging were used to characterize the effect of Mg^2+ on hydrate of cement pastes. The experimental results show that in ample space, periclase forms octahedron structure, and subhedral or anhedral crystal is formed in limited space. Due to the accelerated burning temperature and prolonged holding time, coarse pericalase crystals are formed. Mg(OH)2 particle thickness increases due to faster crystal growth rate along c axis at later age. Mg^2+can substitute Ca^2+ in C-S-H or C-A-H to form magnesium silicate hydrate(M-S-H) or magnesium aluminate hydrate(M-A-H), and the substitution extent for C-A-H is higher than that for C-S-H. Cured in 80 ℃ water, the decalcification rate of C-A-H in pastes is higher than that cured in 50 ℃ water. M-A-H with an atomic Mg/Al ratio of 2 is formed through substitution of Ca by Mg in C-A-H.展开更多
In this work,magnesium silicate-based sulfonated polystyrene sphere composites(SPS/MgSi)were synthesized by one-step(SMD1)and two-step(SMD2)methods.For SMD1,MgSi particles were densely assembled on the surface of SPS,...In this work,magnesium silicate-based sulfonated polystyrene sphere composites(SPS/MgSi)were synthesized by one-step(SMD1)and two-step(SMD2)methods.For SMD1,MgSi particles were densely assembled on the surface of SPS,assisted by complexation between Fe^3+and hydroxyl phenol.For SMD2,SPS/SiO2 was firstly obtained by the same method as SMD1,and then SPS/SiO2 was transformed directly to SPS/MgSi under hydrothermal conditions.Therefore,MgSi obtained by the two-step method had an interwoven structure.Compared to SPS,MgSi and SMD1,SMD2 presented a larger specific surface area and more negative surface charges.Therefore,SMD2 showed superior adsorption performance toward CIP with concentrations of 5,10 and 50 mg/L,and for 50 mg/L,the equilibrium adsorption capacity could reach 329.7 mg/g.The adsorption process is fast and can be described by the pseudo-second-order kinetic model.The relationship between pH value and Zeta potential demonstrated that electrostatic interaction dominated the adsorption process.In addition,competitive adsorption showed that the effect of Na^+was negligible but the effect of Ca^2+was dependent on its concentration.Humid acid(HA)could slightly promote the absorption of CIP by SMD2.After five rounds of adsorption-desorption,the equilibrium adsorption capacity of SMD2 still remained at 288.6 mg/L for 50 mg/L CIP.Notably,SMD2 presented likewise superior adsorption capacity for CIP with concentrations of 10 and 50 mg/L in Minjiang source water.All the results indicated that this synthesis method is universal and that SMD2 has potential as an adsorbent for CIP removal from aquatic environments.展开更多
Glasses of the SiO_2-Al_2O_3-BaO-MgO and SiO_2-Al_2O_3-ZrO_2-CaO-Na_2O systems were synthesized in the perspective to apply them as sealants in SOFC at operating temperatures of 700-900 °C. Thermal properties of ...Glasses of the SiO_2-Al_2O_3-BaO-MgO and SiO_2-Al_2O_3-ZrO_2-CaO-Na_2O systems were synthesized in the perspective to apply them as sealants in SOFC at operating temperatures of 700-900 °C. Thermal properties of the chosen glass compositions and their compatibility with the SOFC materials(YSZ-electrolyte and alloy-interconnector Crofer22 APU, 15Х25Т) were investigated by means of synchronic thermal analysis and high-temperature dilatometry. The elemental analysis was performed by atomic emission spectroscopy. The average values of the temperature coefficients of the linear extension are 10.0×10^(-6) °С^(-1) for glass 45%SiO_2-15%Al_2O_3-25%BaO-15%MgO and 9.5×10^(-6) °С^(-1) for glass 60%SiO_2-10%Al_2O_3-10%ZrO_2-5%CaO-15%Na_2O. The gluing microstructure in YSZ/glass/Crofer22 APU was studied by scanning electron microscopy. The crystallization process of silicate phases was revealed to occur in the SiO_2-Al_2O_3-BaO-MgO glass. The analysis of the crystallization products was performed by Raman spectroscopy and X-ray diffraction. Glassy ceramics was proved to possess better parameters in comparison with amorphous glass to be used as a sealant in electrochemical sensors and oxygen sensors. The SiO_2-Al_2O_3-ZrO_2-CaO-Na_2O low-temperature amorphous glass can be applied in SOFC.展开更多
The bone marrow is essential for immune function,hematopoiesis,and skeletal system.The emergence of bone marrow organoids(BMOs)holds promise for addressing bone-related deficiencies,although maintaining BMOs homeostas...The bone marrow is essential for immune function,hematopoiesis,and skeletal system.The emergence of bone marrow organoids(BMOs)holds promise for addressing bone-related deficiencies,although maintaining BMOs homeostasis is still challenging,and their efficacy for tissue regeneration remains uncertain.Silicate biomaterials can provide distinctive biochemical clues by releasing bioactive ions,which are beneficial for regulating stem cell behaviors and developing cell functions.In this study,harnessing the bioactivities of silicate biomaterials,we engineered functional BMOs through the culture of mesenchymal stem cells(MSCs)and endothelial cells in a chemically defined medium,incorporating with calcium silicate nanowires(CS)and magnesium silicate nanospheres(MSS).The resulting BMOs demonstrated robust preservation of endothelial networks,increased self-renewal of the mesenchymal compartment,and positive effects on hematopoietic stem cells.Co-culture experiments revealed that the engineered BMOs can significantly improve the activities of chondrocytes,MSCs,and Schwann cells,which are pivotal for tissue regeneration.Furthermore,the silicate biomaterials upregulated gene expression and signaling pathways in the domains of osteogenesis and angiogenesis.In a rabbit osteochondral repair model,BMOs induced by MSS notably enhanced osteochondral regeneration.Our study reveals the critical role of silicate biomaterials in augmenting BMOs homeostasis and function,providing an innovative and compelling strategy for future tissue regeneration.展开更多
An understanding of the thermodynamics of the complexation process utilized in sustaining drug release in clay matrices is of great importance.Several characterisation techniques as well as isothermal calorimetry were...An understanding of the thermodynamics of the complexation process utilized in sustaining drug release in clay matrices is of great importance.Several characterisation techniques as well as isothermal calorimetry were utilized in investigating the adsorption process of a model cationic drug(diltiazem hydrochloride,DIL)onto a pharmaceutical clay system(magnesium aluminium silicate,MAS).X-ray powder diffraction(XRPD),attenuated total reflectance Fourier transform infrared spectroscopy(ATRFTIR)and optical microscopy confirmed the successful formation of the DIL-MAS complexes.Drug quantification from the complexes demonstrated variable behaviour in the differing media used with DIL degrading to desacetyl diltiazem hydrochloride(DC-DIL)in the 2 M HCl media.Here also,the authors report for the first time two binding processes that occurred for DIL and MAS.A competitor binding model was thus proposed and the thermodynamics obtained suggested their binding processes to be enthalpy driven and entropically unfavourable.This information is of great importance for a formulator as care and consideration should be given with appropriate media selection as well as the nature of binding in complexes.展开更多
In the current work,forsterite samples with different surface area were investigated for its antibacterial activity.Dissolution studies show that the lower degradation of forsterite compared to other silicate bioceram...In the current work,forsterite samples with different surface area were investigated for its antibacterial activity.Dissolution studies show that the lower degradation of forsterite compared to other silicate bioceramics,which is a desirable property for repairing bone defects.Forsterite scaffold shows superior compressive strength than the cortical bone after immersion in simulated body fluid.Bactericidal tests indicate that the forsterite had inhibition effect on the growth of clinical bacterial isolates.Forsterite may be a suitable candidate material for load bearing applications with enhanced mechanical properties and lower degradation rate.展开更多
基金support from the National Natural Science Foundation of China(grant number 52075544)Innovation Funds of Jihua Laboratory(X220971UZ230)+1 种基金Basic and Applied Basic Research Foundation of Guangdong Province(2022A1515110649)Funds from Research Platforms of Guangdong Higher Education Institutes(2022ZDJS038).
文摘Efficient lubrication of magnesium alloys is a highly challenging topic in the field of tribology.In this study,magnesium silicate hydroxide(MSH)nanotubes with serpentine structures were synthesized.The tribological behavior of AZ91D magnesium alloy rubbed against GCr15 steel was studied under lubricating oil with surface-modified MSH nanotubes as additives.The effects of the concentration,applied load,and reciprocating frequency on the friction and wear of the AZ91D alloy were studied using an SRV-4 sliding wear tester.Results show a decrease of 18.7–68.5%in friction coefficient,and a reduction of 19.4–54.3%in wear volume of magnesium alloy can be achieved by applying the synthetic serpentine additive under different conditions.A suspension containing 0.3 wt.%MSH was most efficient in reducing wear and friction.High frequency and medium load were more conducive to improving the tribological properties of magnesium alloys.A series of beneficial physical and chemical processes occurring at the AZ91D alloy/steel interface can be used to explain friction and wear reduction based on the characterization of the morphology,chemical composition,chemical state,microstructure,and nanomechanical properties of the worn surface.The synthetic MSH,with serpentine structure and nanotube morphology,possesses excellent adsorbability,high chemical activity,and good self-lubrication and catalytic activity.Therefore,physical polishing,tribochemical reactions,and physicalchemical depositions can occur easily on the sliding contacts.A dense tribolayer with a complex composition and composite structure was formed on the worn surface.Its high hardness,good toughness and plasticity,and prominent lubricity resulted in the improvement of friction and wear,making the synthetic MSH a promising efficient oil additive for magnesium alloys under boundary and mixed lubrication.
基金the Doctoral Research Startup Fund of Hubei University of Science and Technology(Grant No.BK202504)the Natural Science Foundation of Liaoning Province(Grant No.2023-MS-115).
文摘Aqueous zinc-based energy storage systems offer high theoretical specific capacity,low cost,intrinsic safety,and environmental compatibility,positioning them as promising candidates for next-generation energy storage and conversion technologies.However,issues such as zinc dendrite growth,hydrogen evolution reaction(HER),and surface passivation hinder their practical deployment.To address these challenges,a hollow nanotubular magnesium silicate(denoted MgSi)interfacial layer was constructed on the zinc metal anode(Zn@MgSi).The unique layer structure and negatively charged surface of MgSi facilitate the desolvation of[Zn(H_(2)O)_(6)]^(2+)by stripping water molecules,while temporarily immobilizing Zn^(2+)to suppress random diffusion.The combined effects of the electric field-guided Zn^(2+)distribution and rapid ion transport through the layer structure co-regulate Zn^(2+)flux,leading to uniform,dendrite-free zinc deposition.Consequently,the Zn@MgSi symmetric cell demonstrates a high Zn^(2+)transference number(0.64),extended cycling life exceeding 1600 h at 1 mA cm^(−2),and stable operation for 200 h at 5 mA cm^(−2).Furthermore,zinc-ion hybrid capacitors employing Zn@MgSi electrodes exhibit excellent cycling stability over 5000 cycles.This work highlights the efficacy of artificial interfacial layers in stabilizing zinc metal anodes and provides valuable insights into the development of advanced aqueous zinc-ion energy storage systems.
文摘Batch adsorption from aqueous solutions in a slightly basic medium of Methylene Blue, up to 2500 mg/L, onto synthetic magnesium silicate （Florisil） of three particle size ranges （mean diameters of 112, 200 and 425 μm） was compared to the corresponding adsorption onto activated carbon and Amberlite XAD-2. The best fit of the kinetic results was achieved by a pseudo second-order equation. The equilibrium data were found to be well represented by the Langmuir isotherm equation. Amberlite XAD-2, an unspecific adsorbent capable of adsorbing exclusively through a surface effect, exhibited a poor dye uptake, confirming that the adsorption mechanism on Florisil was due to electrostatic attraction and ion exchange. Moreover, the comparison between Florisil and the other adsorbents was performed on the basis of the evaluation of the surface area and pore volume occupied by the adsorbed dye.
基金Funded by Natural Science Basic Research Plan in Shaanxi Province of China (Nos.2021JQ-500, 2021GY-203, 2023-JCYB-096)Shaanxi Provincial Education Department of Key Scientific Research Plan (No.20JS079)Shaanxi Provincial Education Department of Normal Scientific Research Plan (No.20JK0727)。
文摘In order to expand the advantages of strong durability and high compressive strength of calcium silicate hydrates(C-S-H),at the same time to make up for the poor early mechanical strength of magnesium silicate hydrates (M-S-H),we present the features and advantages of C-S-H and M-S-H and a comprehensive review of the progress on CaO-MgO-SiO_(2)-H_(2)O.Moreover,we systematically describe natural calcium and magnesium silicate minerals and thermodynamic properties of CaO-MgO-SiO_(2)-H_(2)O.The effect of magnesium on C-S-H and calcium on M-S-H is summarized deeply;the formation and structural feature of CaO-MgO-SiO_(2)-H_(2)O is also explained in detail.Finally,the development of calcium and magnesium silicate hydrates in the future is pointed out,and the further research is discussed and estimated.
基金financially supported by the National Key R&D Program of China(No.2023YFB2503801)the Key Program of the National Natural Science Foundation of China(No.52231009)+1 种基金the National Science Foundation of China(No.52302253)the Key R&D Program of Hubei Province(No.2023BAB028)。
文摘Solid-state batteries with solid polymer electrolytes are considered the most promising due to their high energy density and safety advantages.However,their development is hindered by the limitations of polymer electrolytes,such as low ionic conductivity,poor mechanical strength and inadequate fire resistance.This study presents a thin polyvinylidene fluoride-based composite solid electrolyte film(25μm incorporating twodimensional modified lipophilic lithium magnesium silicate(LLS)as additives with good dispersibility.The incorporation of LLS promotes grain refinement in polyvinylidene fluoride(PVDF),enhances the densification of electrolyte films,increases the tensile strength to10.42 MPa and the elongation to 251.58%,improves ion transport interfac e,and facilitates uniform deposition of lithium ions.Furthermore,LLS demonstrates strong adsorption ability,promoting the formation of solvated molecules,resulting in high ionic conductivity(2.07×10^(-4)S·cm^(-1)at 30℃)and a stable lithium/electrolyte interface.Symmetric Li//Li cells assembled with the thin composite electrolytes exhibit stable cycling for2000 h at 0.1 mA·cm^(-2)and 0.05 mAh·cm^(-2).Additionally,the LiFePO_(4)//Li battery shows a capacity retention rate of99.9%after 200 cycles at 0.5C and room temperature.
文摘This study aims to investigate the behavior of alkali activated mortar,which is made of naturally available magnesium silicate as source material.For magnesium silicate,ultrafine natural steatite powder(UFNSP)is used as the primary source of binder,and the activation is initiated through the alkali liquid which is proportioned in various combinations of silicate to hydroxide ratio(Na_(2)SiO_(3)/Na OH)ratio,and this ratio in this study varies from 1 to 3.The UFNSP is calcined at two difierent temperatures,700 and 1000℃.The mortar mix is proportioned as 1:3 between powder and the fine aggregate,and the mortar is prepared with hydroxide molarity(M)of 10 M.The mortar is cured for 48 hours at 60℃and the compressive strength was studied.All the mix were studied for its microstructural behavior along with compressive strength.The mix proportion of the mortar,and the results obtained through microstructural characterization were combinedly formed as input for artificial neural network(ANN)predictive modelling.The model is designed to predict the compressive strength,which is trained through Bayesian regularization algorithm with varying hidden neurons of 7 to 10.This experimental and predictive study shows that the strength is influenced by both Na_(2)SiO_(3)/Na OH ratio and calcination process.And the ANN is influenced by mainly calcination temperature and uncorrelation occurs in selected samples of 1000℃calcined UFNSP mix.
基金supported by Areas of Excellence from the Research Grants Council of Hong Kong(AoE/M-402/20)NSFC/RGC Joint Research Scheme(N_CUHK405/21)+2 种基金Research Impact Fund(R4034-23F)Health and Medical Research Fund(HMRF,09203786)IdeaBooster Fund(IDBF24MED10)。
文摘Given the confluence of dysregulated inflammation,vasculopathy,and neuropathy,diabetic wounds pose a significant clinical challenge.Commercially available wound dressings often lack sufficient bioactivity,failing to meet clinical demands.Herein,we developed a PCL-PLLA-MgSiO_(3)(PP-MgSi)patch with promising therapeutic effects.The PP-MgSi composite patch was manufactured via electrospinning and characterized by controllable degradation and local release of Mg^(2+)and SiO_(3)^(2−).The patch showed favorable in vitro biocompatibility and bioactivity,notably increased angiogenesis,myelination,and neurite outgrowth.In type 2 diabetic mice,the PP-MgSi patch exhibited MgSi dose-dependent effects on enhancing diabetic wound healing by modulating the expression of TNF-α,iNOS,and CD206 to balance inflammation,while boosting CD31 andβ3-tubulin levels to promote neurovascularization.With the significant suppression of pro-inflammatory-related TNF and IL-17 pathways,while activating the peripheral nerve-associated axon guidance pathway,blood vessel-associated HIF-1αand VEGF pathways,the PP-MgSi patch ultimately achieved accelerated healing compared to the control group.Ultimately,the PP-MgSi patch exhibited an accelerated repair rate,with comparable neovascularization and superior peripheral nerve regeneration capacity compared to three representative commercially available products.This proof-of-concept work presents a promising bioactive PP-MgSi patch for future clinical diabetic wound management,particularly in terms of its neurovascular network recovery properties.
基金funded by Beijing Engineering Center for Hierarchical Catalysts,Nanjiang Technology Project(grant No.2023AB028)Open Laboratory of State Key Laboratory of Organic and Inorganic Composites(grant No.oic-202301006)+1 种基金the CSC scholarship program(grant No.2018GXz021558)distinguished professor of Kunlun Scholars in Tarim University.
文摘Hierarchical porous magnesium silicate hydrate (MSH) microspheres composed of sheets are successfully developed under facile conditions using a hard template. The role of hexadecyltrimethylammonium bromide (CTAB) on the formation and adsorption behavior was also observed for the methyl orange and methylene blue. The formed MSH possesses a surface area of 453.24 m^(2)/g, an average pore size of 6.38 nm, and a pore volume of 0.75 cm^(3)/g without CTAB. Based on the role of CTAB and the change in the ratio of Mg/Si, the MSH retained its sphere-like structure with a variation in pore parameters. The formed MSH was used as an adsorbent to remove methylene blue and methyl orange. The pseudo-second-order kinetic and Langmuir Isotherm models are well-fitted, with a 256.4 mg/g removal capacity and 84.2 mg/g for methylene blue and methyl orange, respectively. The modified MSH with CTAB played a positive role for the methyl orange and a negative role for the methylene blue regarding removal performance.
基金This study was financially supported by the National Science and Technology Major Project(No.2017-VI-0010-0081)the Program of the Ministry of Education of China for Introducing Talents of Discipline to Universities(No.B17002)+2 种基金the National Natural Science Foundation of China(No.51901011)the“Freigeist”Fellowship of the Volkswagenstiftung on“Volcanic Ash Deposition in Jet Engines”(VADJEs,No.89705)China Scholarship Council(CSC).
文摘Airborne silicate pollutants in flight corridors pose a serious threat to aviation safety whose severity is directly linked to the wettability of molten silicates on thermal barrier coatings(TBCs)at high temperatures(1200–2000℃).Despite its importance,the wettability of silicate melt on TBCs has not been well investigated.In particular,the surface morphology characteristics of TBCs can be expected to have a first-order effect on the wettability of silicate melt on such TBCs.Here,a series of atmospheric plasma spray(APS)yttria-stabilized zirconia(YSZ)TBCs with varying surface roughness were generated through the application of mechanical polishing.The metastable nonwetting behavior of three representative types of airborne silicate ash(volcanic ash,fly ash and a synthetic calcium–magnesium–aluminum–silicates(CMAS)powder)on these TBCs with varying surface roughness was investigated.It was observed that the smoother the surface of TBCs was,the larger the contact angle was with the molten silicate melts,and consequently,the smaller the area of damage was on the TBCs.Thus,the reduction in TBCs surface roughness(here via mechanical polishing)led to an improvement in the wetting and spreading resistance of TBCs to silicate melts at high temperature.In support of these observations and conclusions,the surface morphology of the TBC(both before and after polishing)had been characterized,and the mechanism of the surface roughness-dependence of wettability had been discussed.These results should contribute to reducing the deposition rate of silicate melt on TBCs,thus extending the lifetime of turbine blades and reducing maintenance costs.
基金Project(52264022)supported by the National Natural Science Foundation of ChinaProject(BGRIMM-KJSKL-2025-17)supported by the Open Foundation of State Key Laboratory of Mineral Processing,China。
文摘Finding appropriate flotation reagents to separate copper-nickel sulfide ores from various magnesium silicate gangue minerals has always been a challenge in the mineral processing industry.This study introduced xanthan gum(XG)as a non-toxic and environmentally friendly depressant of talc,olivine,and serpentine.The effects and mechanisms of XG on the aggregation and flotation behavior of talc,olivine and serpentine were investigated by flotation tests,sedimentation tests,IC-FBRM particle size analysis tests,adsorption quantity tests,Fourier transform infrared spectroscopy(FTIR)tests,X-ray photoelectron spectroscopy(XPS)analysis tests and Zeta potential tests.The flotation results indicated that when the three minerals were mixed,XG caused the talc-serpentine aggregation in the solution to shift to olivine-serpentine aggregation,with the remaining XG adsorbing on talc to depress its flotation.In addition,combining XPS and zeta potential tests,the-OH(hydroxyl)groups in XG molecules preferentially adsorbed on Mg sites on the surface of olivine through chemical bonding.The surface potential of olivine significantly shifted to a more negative value,with the negative charge on the olivine surface far exceeding that on the talc surface.This resulted in an increased aggregation effect between positively charged serpentine and negatively charged olivine due to enhanced electrostatic forces.
文摘Long afterglow photoluminescent materials Sr2MgSi2O7 doped with Eu2+, Dy3+ were prepared by sol-gel method. The synthesized samples were characterized by X-ray diffraction. The excitation spectrum, emission spectrum and long decay curve were measured and analyzed. XRD pattern indicates that phosphor is with Sr2MgSi2O7 crystal structure. The wide range of excitation wavelength indicates that luminescent material can be excited by light from ultraviolet ray to visible light. The main peak of emission spectrum is located at 466 nm. Sample excited by visible light can emit bright blue light, and the afterglow time lasts more than 8 h.
基金Funded by the National "973 Project"(2009CB623104)the Fundamental Research Funds for the Central Universities(2009ZZ0044)the Funds of Key Laboratory of Advance Civil Engineering Materials of the Ministry of Education
文摘The paste was prepared by mixing MgO, microsilica and H2O in the presence of water reducer at different reaction ratios and temperatures, and characterized by XRD, DTA, TGA, IR, and solid-state 29Si NMR. The experimental results showed that, besides Mg（OH）2, magnesium silicate hydrate （M-S-H） was formed at a low temperature such as 25 and 50 ℃. At a high temperature of 100 ℃, Mg（OH）2 can be further transformed into M-S-H completely, for instance, within ca. 1 month in an excess of microsilica. The average composition and structure of M-S-H was mainly related to the reaction mixture and curing temperature and was discussed in detail.
文摘It was proved that MgO and MicroSilica can react at room temperature, giving a hardened product primarily comprised of Mg （ OH ）2 and Magnesium Silicate Hydrate （ M- S- H ）. The reaction ratio and process and the chemical composion of M- S- H were studied and analyzed by QXRD and DTA- TG. The experimental results indicate that much Mg（ OH）2 and less M-S-H were formed at early period. After 7 days there is no change in the quantity of Mg（ OH）2, while M-S-H was increased slowly. The chemical composion of M-S-H would vary with the mix proportion in the hydrution process , but M1.32 SH2.37 is finally the approximute form.
基金Project is supported by National High Technology Research and Development Program of China (863 Program) (2002 AA 324060)National Natural Science Foundation of China (10404028)
文摘Sol-gel method was utilized to synthesize two different series of red silicate phosphors : MgSiO3 and Mg2SiO4 powder samples doped with Mn2+, conducted the investigation of red long-lasting phosphor: MgSiO3 : Eu2 + , Dy3+, Mn2+ . TGA curves of the gel precursor for two series depicted that the loss of residual organic groups and NO3 groups occurs below 450℃. According to the XRD patterns, the major diffraction peaks of the MgSiO3 and Mg2SiO4 series are consistent with a proto-enstatite structure (JCPDS No.11-0273) and a forsterite structure (JCPDS No.85-1364) respectively. With the excitation at 415 nm, the red emission band of Mn2+ ions is peaked at 661 nm for MgSiO3:1%(atom fraction) Mn2+ or 644 nm for MgiSiO4: 1 %(atom fraction) Mn2+ . Compared with Mg2SiO4:Mn2+ samples, MgSiO3:Mn2+ samples exhibit higher luminescence intensity and higher quenching concentration. In addition, the two series co-doped with Eu2+ , Dy3+ , Mn2+ were also prepared. Photo-luminescence and afterglow properties of the two co-doped series were analyzed, which show that MgSiO3: Eu2 + , Dy3+ , Mn2+ is more suitable for a red long-lasting phosphor.
基金Funded by the National Key R&D Program of China(2016YFB0303400,2017YFB0309903-03)the Natural Science Foundation of Shaaxi Province of China(2017JM5097)
文摘Crystallization characteristic of periclase in clinker and effect of Mg^2+ on hydrate of cement pastes were investigated. Morphologies and relative content of periclase were characterized with scanning electron microscopy and X-ray diffraction. Derivative thermogravimetry analysis and backscattered electron imaging were used to characterize the effect of Mg^2+ on hydrate of cement pastes. The experimental results show that in ample space, periclase forms octahedron structure, and subhedral or anhedral crystal is formed in limited space. Due to the accelerated burning temperature and prolonged holding time, coarse pericalase crystals are formed. Mg(OH)2 particle thickness increases due to faster crystal growth rate along c axis at later age. Mg^2+can substitute Ca^2+ in C-S-H or C-A-H to form magnesium silicate hydrate(M-S-H) or magnesium aluminate hydrate(M-A-H), and the substitution extent for C-A-H is higher than that for C-S-H. Cured in 80 ℃ water, the decalcification rate of C-A-H in pastes is higher than that cured in 50 ℃ water. M-A-H with an atomic Mg/Al ratio of 2 is formed through substitution of Ca by Mg in C-A-H.
基金This work was supported by the National Natural Science Foundation of China(Nos.21577018 and 21477128)and the National Science Foundation of Fujian Province(No.2016J01223).
文摘In this work,magnesium silicate-based sulfonated polystyrene sphere composites(SPS/MgSi)were synthesized by one-step(SMD1)and two-step(SMD2)methods.For SMD1,MgSi particles were densely assembled on the surface of SPS,assisted by complexation between Fe^3+and hydroxyl phenol.For SMD2,SPS/SiO2 was firstly obtained by the same method as SMD1,and then SPS/SiO2 was transformed directly to SPS/MgSi under hydrothermal conditions.Therefore,MgSi obtained by the two-step method had an interwoven structure.Compared to SPS,MgSi and SMD1,SMD2 presented a larger specific surface area and more negative surface charges.Therefore,SMD2 showed superior adsorption performance toward CIP with concentrations of 5,10 and 50 mg/L,and for 50 mg/L,the equilibrium adsorption capacity could reach 329.7 mg/g.The adsorption process is fast and can be described by the pseudo-second-order kinetic model.The relationship between pH value and Zeta potential demonstrated that electrostatic interaction dominated the adsorption process.In addition,competitive adsorption showed that the effect of Na^+was negligible but the effect of Ca^2+was dependent on its concentration.Humid acid(HA)could slightly promote the absorption of CIP by SMD2.After five rounds of adsorption-desorption,the equilibrium adsorption capacity of SMD2 still remained at 288.6 mg/L for 50 mg/L CIP.Notably,SMD2 presented likewise superior adsorption capacity for CIP with concentrations of 10 and 50 mg/L in Minjiang source water.All the results indicated that this synthesis method is universal and that SMD2 has potential as an adsorbent for CIP removal from aquatic environments.
基金supported by the program “Fundamental research program for the development of the Arctic zone of the Russian Federation”the Russian Foundation for Basic Research, project No. 14-29-04009+2 种基金supported by Act 211 of Government of the Russian Federation, agreement No. 02.A03.21.0006Russian President scholarship 2015-2017 CⅡ-1572.2015.1 and СⅡ-1663.2015.1the co-worker of Research and Advanced Development in the framework of the project “Development and creation of high-technological manufactory of autonomic multipurpose power sources based of domestic high-technological solid oxide fuel cells” (No. 02.G25.31.0198 by 27.04.2016) under financial support of the Ministry of Education and Science of Russian Federation in accordance with Government of Russian Federation Decree by 09.04.2010 N 218
文摘Glasses of the SiO_2-Al_2O_3-BaO-MgO and SiO_2-Al_2O_3-ZrO_2-CaO-Na_2O systems were synthesized in the perspective to apply them as sealants in SOFC at operating temperatures of 700-900 °C. Thermal properties of the chosen glass compositions and their compatibility with the SOFC materials(YSZ-electrolyte and alloy-interconnector Crofer22 APU, 15Х25Т) were investigated by means of synchronic thermal analysis and high-temperature dilatometry. The elemental analysis was performed by atomic emission spectroscopy. The average values of the temperature coefficients of the linear extension are 10.0×10^(-6) °С^(-1) for glass 45%SiO_2-15%Al_2O_3-25%BaO-15%MgO and 9.5×10^(-6) °С^(-1) for glass 60%SiO_2-10%Al_2O_3-10%ZrO_2-5%CaO-15%Na_2O. The gluing microstructure in YSZ/glass/Crofer22 APU was studied by scanning electron microscopy. The crystallization process of silicate phases was revealed to occur in the SiO_2-Al_2O_3-BaO-MgO glass. The analysis of the crystallization products was performed by Raman spectroscopy and X-ray diffraction. Glassy ceramics was proved to possess better parameters in comparison with amorphous glass to be used as a sealant in electrochemical sensors and oxygen sensors. The SiO_2-Al_2O_3-ZrO_2-CaO-Na_2O low-temperature amorphous glass can be applied in SOFC.
基金supported by the National Key Research and Development Program of China(2023YFB3813000)the National Natural Science Foundation of China(32225028)+2 种基金Joint Research Unit Plan of Chinese Academy of Sciences(121631ZYLH20240014)Jiangsu Province Basic Research Key Program(BK20243003),Science and Technology of Shanghai municipality(24520750100)Natural Science Foundation of Shanghai(25ZR1401374).
文摘The bone marrow is essential for immune function,hematopoiesis,and skeletal system.The emergence of bone marrow organoids(BMOs)holds promise for addressing bone-related deficiencies,although maintaining BMOs homeostasis is still challenging,and their efficacy for tissue regeneration remains uncertain.Silicate biomaterials can provide distinctive biochemical clues by releasing bioactive ions,which are beneficial for regulating stem cell behaviors and developing cell functions.In this study,harnessing the bioactivities of silicate biomaterials,we engineered functional BMOs through the culture of mesenchymal stem cells(MSCs)and endothelial cells in a chemically defined medium,incorporating with calcium silicate nanowires(CS)and magnesium silicate nanospheres(MSS).The resulting BMOs demonstrated robust preservation of endothelial networks,increased self-renewal of the mesenchymal compartment,and positive effects on hematopoietic stem cells.Co-culture experiments revealed that the engineered BMOs can significantly improve the activities of chondrocytes,MSCs,and Schwann cells,which are pivotal for tissue regeneration.Furthermore,the silicate biomaterials upregulated gene expression and signaling pathways in the domains of osteogenesis and angiogenesis.In a rabbit osteochondral repair model,BMOs induced by MSS notably enhanced osteochondral regeneration.Our study reveals the critical role of silicate biomaterials in augmenting BMOs homeostasis and function,providing an innovative and compelling strategy for future tissue regeneration.
文摘An understanding of the thermodynamics of the complexation process utilized in sustaining drug release in clay matrices is of great importance.Several characterisation techniques as well as isothermal calorimetry were utilized in investigating the adsorption process of a model cationic drug(diltiazem hydrochloride,DIL)onto a pharmaceutical clay system(magnesium aluminium silicate,MAS).X-ray powder diffraction(XRPD),attenuated total reflectance Fourier transform infrared spectroscopy(ATRFTIR)and optical microscopy confirmed the successful formation of the DIL-MAS complexes.Drug quantification from the complexes demonstrated variable behaviour in the differing media used with DIL degrading to desacetyl diltiazem hydrochloride(DC-DIL)in the 2 M HCl media.Here also,the authors report for the first time two binding processes that occurred for DIL and MAS.A competitor binding model was thus proposed and the thermodynamics obtained suggested their binding processes to be enthalpy driven and entropically unfavourable.This information is of great importance for a formulator as care and consideration should be given with appropriate media selection as well as the nature of binding in complexes.
基金This research was financially supported by Vellore Institute of Technology Research Grants for Engineering,Management,and Science(VITRGEMS)The authors thank DST-FIST for the XRD and SEM/EDX characterization.Also thankful to CAMPT-VIT for Mechanical testing.
文摘In the current work,forsterite samples with different surface area were investigated for its antibacterial activity.Dissolution studies show that the lower degradation of forsterite compared to other silicate bioceramics,which is a desirable property for repairing bone defects.Forsterite scaffold shows superior compressive strength than the cortical bone after immersion in simulated body fluid.Bactericidal tests indicate that the forsterite had inhibition effect on the growth of clinical bacterial isolates.Forsterite may be a suitable candidate material for load bearing applications with enhanced mechanical properties and lower degradation rate.
