Oxygen evolution reaction(OER)is a key step in hydrogen production by water electrolysis technology.How-ever,developing efficient,stable,and low-cost OER electrocatalysts is still challenging.This article presents the...Oxygen evolution reaction(OER)is a key step in hydrogen production by water electrolysis technology.How-ever,developing efficient,stable,and low-cost OER electrocatalysts is still challenging.This article presents the preparation of a series of novel copper iridium nanocatalysts with heterostructures and low iridium content for OER.The electrochemical tests revealed higher OER of Cu@Ir_(0.3) catalyst under acidic conditions with a generated current density of 10 mA/cm^(2) at only 284 mV overpotential.The corresponding OER mass activity was estimated to be 1.057 A/mgIr,a value 8.39-fold higher than that of the commercial IrO_(2).After 50 h of endurance testing,the Cu@Ir_(0.3) catalyst preserved excellent catalytic activity with a negligible rise in overpotential and maintained a good heterostructures.Cu@Ir_(0.3) The excellent OER activity can be attributed to its heterostructure,as con-firmed by density functional theory(DFT)calculations,indicating that Cu@Ir The coupling between isoquanta causes charge redistribution,optimizing the adsorption energy of unsaturated Ir sites for oxygen intermediates and reducing the energy barrier of OER free energy determining the rate step.In summary,this method provides a new approach for designing efficient,stable,and low iridium content OER catalysts.展开更多
Corrosion behaviour of the studied Ti12Mo and Ti60Ta alloys with the same Mo equivalent values （12%, mass fraction） together with the currently used metallic biomaterials Cp-Ti were investigated for dental applicati...Corrosion behaviour of the studied Ti12Mo and Ti60Ta alloys with the same Mo equivalent values （12%, mass fraction） together with the currently used metallic biomaterials Cp-Ti were investigated for dental applications. The electrochemical properties of the samples were examined using electrochemical techniques： such as open-circuit potential, potentiodynamic polarization curves and electrochemical impedance spectroscopy （EIS）, in two electrochemical media of artificial saliva and fluoridated artificial saliva （0.1%fluoride ions, F-） at 37 °C. Fluoride is commonly included in toothpastes, odontological gels and dental rinses to prevent dental caries and relieve dental sensitivity. The passive behaviour for all the titanium samples is observed for both solutions. The Ti60Ta alloy appears to possess superior corrosion resistance than the Ti12Mo and Cp-Ti in both electrochemical media.展开更多
Atomically dispersed metal sites(ADMSs)play key roles in electrochemical energy conversion.The covalent organic frameworks(COFs)enable the precise control of the chemical compositions and structures at the molecular l...Atomically dispersed metal sites(ADMSs)play key roles in electrochemical energy conversion.The covalent organic frameworks(COFs)enable the precise control of the chemical compositions and structures at the molecular level,making them ideal substrates for supporting ADMSs.In this review,we systematically summarize the recent progress on the design and synthesis of ADMSs in COFs,including embedding molecular catalysts into COFs,immobilizing ADMSs on heteroatom-containing COFs,and preparing COF-derived carbon materials through pyrolysis.The electrocatalytic performance of the resulting catalysts is presented for various electrochemical reactions,involving oxygen reduction reaction(ORR),carbon dioxide reduction reaction(CO_(2)RR),oxygen evolution reaction(OER),hydrogen evolution reaction(HER),and nitrogen reduction reaction(NRR).The modulation strategies of AMDSs in COFs for enhanced activity,selectivity,and stability are highlighted,together with a perspective of the current challenges and the future opportunities in this field.展开更多
The cognition of active sites in the Ni-based catalysts plays a vital role and remains a huge challenge in improving catalytic performance of low temperature CO_(2) dry reforming of methane(LTDRM).In this work,typical...The cognition of active sites in the Ni-based catalysts plays a vital role and remains a huge challenge in improving catalytic performance of low temperature CO_(2) dry reforming of methane(LTDRM).In this work,typical catalysts of SiO_(2) and γ-Al_(2)O_(3) supported Ni and Ni-Ce were designed and prepared.Importantly,the difference in the chemical speciations of active sites on the Ni-based catalysts is revealed by advanced characterizations and further estimates respective catalytic performance for LTDRM.Results show that larger[Ni0-]particles mixed with[Ni-O-Sin])species on the Ni/SiO_(2)(R)make CH_(4) excessive decomposition,leading to poor activity and stability.Once the Ce species is doped,however,superior activity(59.0%CH_(4) and 59.8%CO_(2) conversions),stability and high H_(2)/CO ratio(0.96)at 600℃ can be achieved on the Ni-Ce/SiO_(2)(R),in comparison with other catalysts and even reported studies.The improved performance can be ascribed to the formation of integral([Ni0_(n))]-[CeⅢ-□-CeⅢ])species on the Ni-Ce/SiO_(2)(R)catalyst,containing highly dispersed[Ni]particles and rich oxygen vacancies,which can synergistically establish a new stable balance between gasification of carbon species and CO_(2) dissocia-tion.With respect to Ni-Ce/γ-Al_(2)O_(3)(R),the Ni and Ce precursors are easily captured by extra-framework Al_(n)-OH groups and further form stable isolated([Ni0_(n))]-[Ni-O-Al_(n)])and[CeⅢ-O-Al_(n)]species.In such a case,both of them preferentially accelerate CO_(2) adsorption and dissociation,causing more car-bon deposition due to the disproportionation of superfuous CO product.This deep distinguishment of chemical speciations of active sites can guide us to further develop new efficient Ni-based catalysts for LTDRM in the future.展开更多
Chemical interaction of Ce-Fe mixed oxides was investigated in methane selective oxidation via methane temperature programmed reduction and methane isothermal reaction tests over Ce-Fe oxygen carriers. In methane temp...Chemical interaction of Ce-Fe mixed oxides was investigated in methane selective oxidation via methane temperature programmed reduction and methane isothermal reaction tests over Ce-Fe oxygen carriers. In methane temperature programmed reduction test, Ce-Fe oxide behaved complete oxidation at the lower temperature and selective oxidation at higher temperatures. Ce-Fe mixed oxides with the Fe content in the range of 0.1~）.5 was able to produce syngas with high selectivity in high-temperature range （800-900 ~C）, and a higher Fe amount over 0.5 seemed to depress the CO formation. In isothermal reaction, complete oxidation oc- curred at beginning following with selective oxidation later. Ce~_xFexO2~ oxygen carriers （x5_0.5） were proved to be suitable for the selective oxidation of methane. Ce-Fe mixed oxides had the well-pleasing reducibility with high oxygen releasing rate and CO selec- tivity due to the interaction between Ce and Fe species. Strong chemical interaction of Ce-Fe mixed oxides originated from both Fe＊ activated CeO2 and Ce3＋ activated iron oxides （FeOm）, and those chemical interaction greatly enhanced the oxygen mobility and selectivity.展开更多
The objective of the study was to investigate the presence and the activity of quantum dots nanoparticles in colored wastewaters.The special interest is devoted to the investigation of their role in the typical treatm...The objective of the study was to investigate the presence and the activity of quantum dots nanoparticles in colored wastewaters.The special interest is devoted to the investigation of their role in the typical treatment of water or wastewater,studying their influence on the effectiveness of applied treatments methods.The standard chemical processes for water treatment and disinfection （direct UV photolysis and direct ozonation） were applied for the degradation of colored organic pollutant,reactive azo dye,in the presence/absence of CdSe/ZnS core-shells quantum dots.The obtained results indicated that investigated nanoparticles inhibit the overall efficiency of applied processes,especially in the case of direct UV photolysis,although catalytic effect might be expected in part due to the semiconductor nature of quantum dots.Such results lead to a conclusion that CdSe/ZnS nanoparticles behave as additional pollutants in the system.They should be removed from the system prior the treatment,because their presence could decrease the efficiency,i.e.,prolong the time of treatment and correspondingly increase the costs of the treatment process.展开更多
The electrochemical behaviours of unrecrystallized and recrystallized Ti12Mo5Ta alloys were compared with those of the unrecrystallized Ti12 Mo alloy and commercial pure titanium（cp-Ti）. Experiments were carried out...The electrochemical behaviours of unrecrystallized and recrystallized Ti12Mo5Ta alloys were compared with those of the unrecrystallized Ti12 Mo alloy and commercial pure titanium（cp-Ti）. Experiments were carried out using physiological 0.9% NaCl solution（pH 2.3） at 37 °C. Very low passive current densities（in order of 10-6 A/cm2） were obtained from the anodic polarization curves, indicating high resistances of all samples in acidified 0.9% Na Cl solution. Scanning electron microscopy（SEM） was employed to observe the surface morphology and all sample surfaces were identically corroded, no pitting, cracks, or other defects appeared on the sample surfaces after anodic potentiodynamic polarization tests. Equivalent circuit was used for modeling the electrochemical impedance spectroscopy（EIS） data, in order to characterize the sample surface and better understand the effect of Mo and Ta addition on the cp-Ti and the effect of recrystallization. The EIS results confirm that all titanium samples exhibit passivity in physiological 0.9% NaCl solution（pH 2.3） at open circuit potential（polarization resistance is around 105 Ω·cm2）. The corrosion resistance of these samples in physiological 0.9% NaCl solution（pH 2.3） at 37 °C is in the following order of recrystallized Ti12Mo5Ta〉 unrecrystallized Ti12Mo5Ta 〉 unrecrystallized Ti12Mo 〉 cp-Ti.展开更多
In order to comprehend the applicability of microwave irradiation for recovering coalbed methane,it is necessary to evaluate the microwave irradiation-induced alterations in coals with varying levels of metamorphism.I...In order to comprehend the applicability of microwave irradiation for recovering coalbed methane,it is necessary to evaluate the microwave irradiation-induced alterations in coals with varying levels of metamorphism.In this work,the carbon molecular sieve combined with KMnO_(4)oxidation was selected to fabricate carbon molecular sieve with diverse oxidation degrees,which can serve as model substances toward coals.Afterwards,the microwave irradiation dependences of pores,functional groups,and highpressure methane adsorption characteristics of model substances were studied.The results indicated that microwave irradiation causes rearrangement of oxygen-containing functional groups,which could block the micropores with a size of 0.40-0.60 nm in carbon molecular sieve;meanwhile,naphthalene and phenanthrene generated by macro-molecular structure pyrolysis due to microwave irradiation could block the micropores with a size of 0.70-0.90 nm.These alterations in micropore structure weaken the saturated methane adsorption capacity of oxidized carbon molecular sieve by 2.91%-23.28%,suggesting that microwave irradiation could promote methane desorption.Moreover,the increased mesopores found for oxidized carbon molecular sieve after microwave irradiation could benefit CH4 diffusion.In summary,the oxidized carbon molecular sieve can act as model substances toward coals with different ranks.Additionally,microwave irradiation is a promising technology to enhance coalbed methane recovery.展开更多
Fe-N-C catalysts are widely considered as promising non-precious-metal candidates for electrocatalytic oxygen reduction reaction(ORR),Yet despite their high catalytic activity through rational modulation,challenges re...Fe-N-C catalysts are widely considered as promising non-precious-metal candidates for electrocatalytic oxygen reduction reaction(ORR),Yet despite their high catalytic activity through rational modulation,challenges remain in their low site density and unsatisfactory mass transfer structure.Herein,we present a structural engineering approach employing a soft-template coating strategy to fabricate a hollow and hierarchically porous N-doped carbon framework anchored with atomically dispersed Fe sites(FeNCh) as an efficient ORR catalyst.The combination of hierarchical porosity and high exterior surface area is proven crucial for exposing more active sites,which gives rise to a remarkable ORR performance with a half-wave potential of 0.902 V in 0.1 m KOH and 0.814 V in 0.1 m HClO_(4),significantly outperforming its counterpart with solid structure and dominance of micropores(FeNC-s).The mass transfer property is revealed by in-situ electrochemical impedance spectroscopy(EIS) measurement.The distribution of relaxation time(DRT) analysis is further introduced to deconvolve the kinetic and mass transport processes,which demonstrates an alleviated mass transport resistance for FeNC-h,validating the effectiveness of structural engineering.This work not only provides an effective structural engineering approach but also contributes to the comprehensive mass transfer evaluation on advanced electrocatalyst for energy conversion applications.展开更多
Physicochemical, functional and digestibility analyses were done of dehydrated quail egg white to determine its possible practical applications. Quail egg white was dehydrated by air convection using one of two temper...Physicochemical, functional and digestibility analyses were done of dehydrated quail egg white to determine its possible practical applications. Quail egg white was dehydrated by air convection using one of two temperatures and times: M1 (65℃, 3.5 h), M2 (65℃, 5.0 h), M3 (70℃, 3.5 h) and M4 (70℃, 5.0 h). Lyophilized quail egg white was used as a standard. All four air-dried treatments had good protein levels (92.56% to 93.96%), with electrophoresis showing the predominant proteins to be lysozyme, ovalbumin and ovotransferin. Denaturation temperatures ranged from 81.16℃ to 83.85℃ and denaturation enthalpy values from 5.51 to 9.08 J/g. Treatments M1-4 had lower water-holding (0.90 - 2.95 g/g) and oil-holding (0.92 - 1.01 g/g) capacities than the lyophilized treatment (4.5 g/g, 1.95 g/g, respectively). Foaming capacity was pH-dependent in all five treatments, with the lowest values at alkaline pH and the highest (153% to 222%) at acid pH (pH 2). Foam stability was lowest at acid pH and highest at alkaline pH. Emulsifying activity in the air-dried treatments was highest at pH 8 (41% - 46%). Emulsion stability was pH-dependent and highest in M3 between pH 2 and 4 (96.16% to 95.74%, respectively). In the air-dried treatments, in vitro protein digestibility was as high as 83.02% (M3).展开更多
The aim of this study was to evaluate the texture of corn dough as well as the nutritional quality and acceptance of corn cakes (tortillas) made either with a readymade commercial corn flour (CCF) or with a traditiona...The aim of this study was to evaluate the texture of corn dough as well as the nutritional quality and acceptance of corn cakes (tortillas) made either with a readymade commercial corn flour (CCF) or with a traditional way (nixtamal) both fortified with lys + tryp (L + T) or with a protein concentrate from Phaseolus lunatus added with L + T (PC + L + T). All treatments were analyzed to investigate the physical properties of the dough and tortillas as well as their physicochemical and nutritional quality. Results showed that cohesion was affected (p tortillas made with nixtamal showed no difference. Adhesion was not affected by treatments. Weight loss increased only in the fortified tortillas made with CCF (p tortillas increased with the fortification being the highest value 0.96 N. Color was not affected in tortillas made with CCF (p tortillas made with CCF and fortified with PC + L + T. Acceptance was greater for tortillas fortified with L+T alone. Protein fortification of tortillas made with either CCF or nixtamal is feasible using either L + T together or in combination with a PC from Phaseolus lunatus improving their nutritional value without negative effects on their physicochemical characteristics or acceptance.展开更多
This review provides a comprehensive overview of natural rubber(NR)composites,focusing on their properties,compounding aspects,and renewable practices involving natural fibre reinforcement.The properties of NR are inf...This review provides a comprehensive overview of natural rubber(NR)composites,focusing on their properties,compounding aspects,and renewable practices involving natural fibre reinforcement.The properties of NR are influenced by the compounding process,which incorporates ingredients such as elastomers,vulcanizing agents,accelerators,activators,and fillers like carbon black and silica.While effective in enhancing properties,these fillers lack biodegradability,prompting the exploration of sustainable alternatives.The potential of natural fibres as renewable reinforcements in NR composites is thoroughly covered in this review,highlighting both their advan-tages,such as improved sustainability,and the challenges they present,such as compatibility with the rubber matrix.Surface treatment methods,including alkali and silane treatments,are also discussed as solutions to improve fibre-matrix adhesion and mitigate these challenges.Additionally,the review highlights the potential of oil palm empty fruit bunch(EFB)fibres as a natural fibre reinforcement.The abundance of EFB fibres and their alignment with sustainable practices make them promising substitutes for conventional fillers,contributing to valuable knowledge and supporting the broader move towards renewable reinforcement to improve sustain-ability without compromising the key properties of rubber composites.展开更多
In this study,Pebax■2533 polymer was used as the continuous phase and UiO-67 was employed as the filler to prepare mixed matrix membranes.UiO-67 is usually synthesized using two ligands:biphenyl-4,4'-dicarboxylat...In this study,Pebax■2533 polymer was used as the continuous phase and UiO-67 was employed as the filler to prepare mixed matrix membranes.UiO-67 is usually synthesized using two ligands:biphenyl-4,4'-dicarboxylate(bpdc)and 2,2'-bipyridine-5,5'-dicarboxylic acid(bpy).In this research,UiO-67 was synthesized not only with these two ligands but also using a mixed ligand approach(50% bpdc and 50% bpy).The synthesized UiOs were incorporated into the polymer matrix at mass percentages ranging from 0% to 2% to form the mixed matrix membranes(MMMs).Membranes containing UiO-67 with mixed ligands exhibited a greater affinity for CO_(2) compared to other membranes.Various analytical techniques,including X-ray diffraction,thermogravimetric analyzer,Fourier transform infrared spectroscope(FTIR),field emission scanning electron micro scope(FESEM),and differential scanning calorimetry,were used to analyze the properties of the prepared membranes.The FTIR spectrum confirmed all desired bands of Pebax?2533 and UiO-67 in the MMMs.The FESEM images showed that the pure Pebax membrane has a uniform structure,and the developed membranes are uniformly incorporated with the synthesized UiO-67 nanoparticles.Gas permeation measurements indicated that CO_(2) permeability and CO_(2)/CH_4 selectivity increased from 402.7 Barrer(1 Barrer=1.33×10^(-14)m^(3)(STP)·m·m^(-2)·s^(-1)·kPa^(-1))and 9.32 for the pure Pebax membrane at 1.0 MPa to 770.1 Barrer and 16.96 in the modified membrane.Additionally,the gas permeation test results demonstrated that adding functionalized porous nanofillers increases the CO_(2)separation performance.Permeability tests at different temperatures revealed that as temperature was raised,at constant pressure,CO_(2) permeability for the membrane containing the mixed ligand increased from 682.2 Barrer to 733.5 Barrer,While CO_(2)/CH_(4) selectivity decreased from 15.46 to 13.43.展开更多
Concurrent activation of lattice oxygen(O_L)and molecular oxygen(O_(2))is crucial for the efficient catalytic oxidation of biomass-derived molecules over metal oxides.Herein,we report that the introduction of ultralow...Concurrent activation of lattice oxygen(O_L)and molecular oxygen(O_(2))is crucial for the efficient catalytic oxidation of biomass-derived molecules over metal oxides.Herein,we report that the introduction of ultralow-loading of Ru single atoms(0.42 wt%)into Mn_(2)O_(3)matrix(0.4%Ru-Mn_(2)O_(3))greatly boosts its catalytic activity for the aerobic oxidation of 5-hydroxymethylfurfural(HMF)to 2,5-furandicarboxylic acid(FDCA).The FDCA productivity over the 0.4%Ru-Mn_(2)O_(3)(5.4 mmol_(FDCA)g_(cat)h^(-1))is 4.9 times higher than the Mn_(2)O_(3).Especially,this FDCAproductivity is also significantly higher than that of existing Ru and Mn-based catalysts.Experimental and theoretical investigations discovered that the Ru single atom facilitated the formation of oxygen vacancy(O_(v))in the catalyst,which synergistically weakened the Mn-O bond and promoted the activation of O_L.The co-presence of Ru single atoms and O_(v)also promote the adsorption and activation of both O_(2)and HMF.Consequently,the dehydrogenation reaction energy barrier of the rate-determining step was reduced via both the O_L and chemisorbed O_(2)dehydrogenation pathways,thus boosting the catalytic oxidation reactions.展开更多
Membrane fouling remains the primary economic barrier to the widespread implementation of membrane bioreactors (MBRs), despite the fact that they lead to the production of high-quality effluent. Operational conditions...Membrane fouling remains the primary economic barrier to the widespread implementation of membrane bioreactors (MBRs), despite the fact that they lead to the production of high-quality effluent. Operational conditions are critical factors influencing membrane fouling. This study aimed to investigate the simultaneous impacts of temperature and hydraulic retention time (HRT) variations on membrane fouling. Experiments were conducted at three different temperatures (18°C, 25°C, and 32°C) and HRTs (6 h, 9 h, and 15 h). The results demonstrated that increases in both temperature and HRT contributed to a reduction in membrane fouling. Additionally, a positive interaction between temperature and HRT was observed in the linear slope variation of membrane permeation, with temperature variations exerting a greater influence on membrane fouling than HRT variations. Fouling factor analysis revealed that increases in temperature and HRT led to decreased concentrations of soluble microbial products (SMP) and extracellular polymeric substances (EPS), particularly carbohydrates, in the activated sludge. Analyses of the cake layer of the membrane indicated that increasing temperature and HRT reduced EPS levels, particularly polysaccharides and proteins;altered primary protein structure;and increased the mean particle size distribution. Ultimately, these changes led to reductions in both reversible and irreversible hydraulic resistances. This study highlights the importance of optimizing operational parameters such as temperature and HRT to enhance membrane performance and treatment efficiency in MBR systems while mitigating fouling.展开更多
Magnetization roasting technology is one of the most representative ways to improve the magnetic separation efficiency and iron recovery of refractory weakly magnetic iron ores.However,utilization of CO-rich or H_(2)-...Magnetization roasting technology is one of the most representative ways to improve the magnetic separation efficiency and iron recovery of refractory weakly magnetic iron ores.However,utilization of CO-rich or H_(2)-rich gas of strong reducibility as reducing agent for magnetization roasting would lead to over-reduction of Fe_(2)O_(3) in the ore to non-magnetic FeO,which makes the magnetism of the roasted ore be lower than its maximum,and hence leads to a lower iron recovery than expected.To explore the possibility of using CH_(4) as reducing agent for controllable reduction of Fe_(2)O_(3) in iron ores to selectively forming magnetic Fe_(3)O_(4),i.e.,for maximizing the magnetism of the reduced ore for efficient iron separation and recovery,a series of fluidized bed reduction tests in CH_(4) were carried out on two iron ores of 55%and 33%iron at different temperatures for different periods of time,and the resultant reduced ore particles were magnetically separated for recovery of iron concentrate.XRD and ICP analyses were performed on all recovered iron concentrates to identify the crystal forms of their iron species and to quantify their iron contents.The results have shown that the controllable reduction by CH_(4) of Fe_(2)O_(3) in the iron ores to strongly magnetic Fe_(3)O_(4) can be realized by controlling the reduction temperature and time condition applied.The resultant concentrates can be fully recovered by magnetic separation in a weak magnetic field of 60 kA/m to attain a maximum iron recovery of 98% for the high-grade ore and that of 65% for the low-grade ore.Besides,the results have also shown that the most critical factor affecting the controllability of the ore reduction process and the selectivity to the generation of magnetic Fe_(3)O_(4)-containing particles is the reduction temperature,and that the upper temperature threshold for the controllable reduction and selective generation of strongly magnetic iron concentrate is about 650℃.展开更多
This study represents an important step forward in the domain of additive manufacturing of energetic materials.It presents the successful formulation and fabrication by 3D printing of gun propellants using Fused Depos...This study represents an important step forward in the domain of additive manufacturing of energetic materials.It presents the successful formulation and fabrication by 3D printing of gun propellants using Fused Deposition Modeling(FDM)technology,highlighting the immense potential of this innovative approach.The use of FDM additive manufacturing technology to print gun propellants is a significant advancement due to its novel application in this field,which has not been previously reported.Through this study,the potential of FDM 3D-printing in the production of high-performance energetic composites is demonstrated,and also a new standard for manufacturability in this field can be established.The thermoplastic composites developed in this study are characterized by a notably high energetic solids content,comprising 70%hexogen(RDX)and 10%nitrocellulose(NC),which surpasses the conventional limit of 60%energetic solids typically achieved in stereolithography and light-curing 3D printing methods.The primary objective of the study was to optimize the formulation,enhance performance,and establish an equilibrium between printability and propellant efficacy.Among the three energetic for-mulations developed for 3D printing feedstock,only two were suitable for printing via the FDM tech-nique.Notably,the formulation consisting of 70%RDX,10%NC,and 20%polycaprolactone(PCL)emerged as the most advantageous option for gun propellants,owing to its exceptional processability,ease of printability,and high energetic performance.展开更多
In this study,non-thermal plasma(NTP)was employed to modify the Cu/TiO_(2)adsorbent to efficiently purify H_(2)S in low-temperature and micro-oxygen environments.The effects of Cu loading amounts and atmospheres of NT...In this study,non-thermal plasma(NTP)was employed to modify the Cu/TiO_(2)adsorbent to efficiently purify H_(2)S in low-temperature and micro-oxygen environments.The effects of Cu loading amounts and atmospheres of NTP treatment on the adsorption-oxidation performance of the adsorbents were investigated.The NTP modification successfully boosted the H_(2)S removal capacity to varying degrees,and the optimized adsorbent treated by air plasma(Cu/TiO_(2)-Air)attained the best H_(2)S breakthrough capacity of 113.29 mg H_(2)S/gadsorbent,which was almost 5 times higher than that of the adsorbent without NTP modification.Further studies demonstrated that the superior performance of Cu/TiO_(2)-Air was attributed to increased mesoporous volume,more exposure of active sites(CuO)and functional groups(amino groups and hydroxyl groups),enhanced Ti-O-Cu interaction,and the favorable ratio of active oxygen species.Additionally,the X-ray diffraction(XRD)and X-ray photoelectron spectroscopy(XPS)results indicated the main reason for the deactivationwas the consumption of the active components(CuO)and the agglomeration of reaction products(CuS and SO_(4)^(2−))occupying the active sites on the surface and the inner pores of the adsorbents.展开更多
Interfacial compatibilization is essential to generate compatible blend structures with synergistically enhanced properties.However,the effect of molecular structure on the reactivity of compatibilizers is not properl...Interfacial compatibilization is essential to generate compatible blend structures with synergistically enhanced properties.However,the effect of molecular structure on the reactivity of compatibilizers is not properly known.This study investigates the compatibilization effect of multifunctional,epoxy-based Joncryl chain extender in blends of polylactide(PLA)and polybutylene adipate-co-terephthalate(PBAT)using PLA with varying D-lactide contents and molecular weights.These PLAs were high molecular weight amorphous PLA(aPLA)with D-content of 12 mol%and semi-crystalline PLA(scPLA)grades with D-contents below 1.5 mol%at both high(h)and low(l)molecular weights.The reactivity of Joncryl was assessed with each individual neat polymer,and its compatibilization effectwas examined in blends at aweight ratio of 75 wt/25wt using small amplitude oscillatory shear(SAOS)rheological analysis.Differential scanning calorimetry(DSC),dynamic mechanical analysis(DMA),tensile and impact tests,as well as scanning electron microscopy(SEM)observations,were conducted to characterize the blends.The addition of Joncryl resulted in remarkable improvements rheological behavior of all neat polymers and noticeably refined PBAT droplets in all blends,particularly in aPLA/PBAT and scPLA(l)/PBAT.The ductility,toughness and impact strength of these blends were significantly enhanced,while their tensile strength and modulus also showed slight improvements.Although the addition of Joncryl retarded the crystallization of the scPLA samples,the scPLA(h)/PBAT blend with Joncryl exhibited the highest thermomechanical performance over a wide temperature range.This was attributed to the higher crystallinity of scPLA(h),which,even in the presence of Joncryl,provided high thermal stability.展开更多
This study focuses on the preparation,and optimization of the nanoemulsions coorporating with pumpkin seed oil,grape seed oil,and grapefruit essential oil using the phase inversion temperature(PIT)technique.The resear...This study focuses on the preparation,and optimization of the nanoemulsions coorporating with pumpkin seed oil,grape seed oil,and grapefruit essential oil using the phase inversion temperature(PIT)technique.The research investigated the impact of surfactant types and concentrations on critical nanoemulsion properties,including droplet size,polydispersity index(PDI),and zeta potential.Using a Box-Behnken Design(BBD)model,the formulation was optimized containing 6.0%plant oils,10.0%Tween 80,2.0%Span 80,and 1.0%lecithin to achieve nano-sized droplets(33.52 nm),with a low PDI(0.205),and a stable zeta potential(15.49 mV).The antioxidant activity,was evaluated through 2,2-diphenyl-1-picrylhydrazyl(DPPH)radical scavenging assays,demonstrating its outstanding efficacy.And the optimized nanoemulsion showed a radical-scavenging capacity exceeding 2250μg ascorbic acid equivalents/g,significantly outperforming non-nanoemulsified oils.Stability testing under various environmental conditions highlighted exceptional robustness,with refrigerated samples maintaining structural integrity,minimal particle size growth,and consistent physicochemical properties over a 30-day storage period.The results suggest that the plant oil-based nanoemulsions exhibit strong antioxidant potential,offering a promising natural treatment for their application in cosmeceutical and therapeutic formulations.展开更多
基金supported by the Major Science and Technology Special Plan of Yunnan Province(Nos.202302AB080012 and 202402AB080004)the National Natural Science Foundation of China(No.22264025)+1 种基金the Basic Research Foundation of Yunnan Province(Nos.202401AS070033 and 202501AT070055)the Reserve talents for young and middleaged academic and technical leaders project of Yunnan Province(No.202405AC350071).
文摘Oxygen evolution reaction(OER)is a key step in hydrogen production by water electrolysis technology.How-ever,developing efficient,stable,and low-cost OER electrocatalysts is still challenging.This article presents the preparation of a series of novel copper iridium nanocatalysts with heterostructures and low iridium content for OER.The electrochemical tests revealed higher OER of Cu@Ir_(0.3) catalyst under acidic conditions with a generated current density of 10 mA/cm^(2) at only 284 mV overpotential.The corresponding OER mass activity was estimated to be 1.057 A/mgIr,a value 8.39-fold higher than that of the commercial IrO_(2).After 50 h of endurance testing,the Cu@Ir_(0.3) catalyst preserved excellent catalytic activity with a negligible rise in overpotential and maintained a good heterostructures.Cu@Ir_(0.3) The excellent OER activity can be attributed to its heterostructure,as con-firmed by density functional theory(DFT)calculations,indicating that Cu@Ir The coupling between isoquanta causes charge redistribution,optimizing the adsorption energy of unsaturated Ir sites for oxygen intermediates and reducing the energy barrier of OER free energy determining the rate step.In summary,this method provides a new approach for designing efficient,stable,and low iridium content OER catalysts.
基金Project (PN-II-ID-PCE-2011-3-0218) supported by the Romanian National Authority for Scientific Research,CNCS-UEFISCDI
文摘Corrosion behaviour of the studied Ti12Mo and Ti60Ta alloys with the same Mo equivalent values （12%, mass fraction） together with the currently used metallic biomaterials Cp-Ti were investigated for dental applications. The electrochemical properties of the samples were examined using electrochemical techniques： such as open-circuit potential, potentiodynamic polarization curves and electrochemical impedance spectroscopy （EIS）, in two electrochemical media of artificial saliva and fluoridated artificial saliva （0.1%fluoride ions, F-） at 37 °C. Fluoride is commonly included in toothpastes, odontological gels and dental rinses to prevent dental caries and relieve dental sensitivity. The passive behaviour for all the titanium samples is observed for both solutions. The Ti60Ta alloy appears to possess superior corrosion resistance than the Ti12Mo and Cp-Ti in both electrochemical media.
基金supported by the National Natural Science Funds(No.21878226)Innovative Research Group Project of the National Natural Science Foundation of China(No.22121004)。
文摘Atomically dispersed metal sites(ADMSs)play key roles in electrochemical energy conversion.The covalent organic frameworks(COFs)enable the precise control of the chemical compositions and structures at the molecular level,making them ideal substrates for supporting ADMSs.In this review,we systematically summarize the recent progress on the design and synthesis of ADMSs in COFs,including embedding molecular catalysts into COFs,immobilizing ADMSs on heteroatom-containing COFs,and preparing COF-derived carbon materials through pyrolysis.The electrocatalytic performance of the resulting catalysts is presented for various electrochemical reactions,involving oxygen reduction reaction(ORR),carbon dioxide reduction reaction(CO_(2)RR),oxygen evolution reaction(OER),hydrogen evolution reaction(HER),and nitrogen reduction reaction(NRR).The modulation strategies of AMDSs in COFs for enhanced activity,selectivity,and stability are highlighted,together with a perspective of the current challenges and the future opportunities in this field.
基金financially supported by the National Natural Science Foundation of China (22006059, 21968015)National Engineering Laboratory for Flue Gas Pollutants Control Technology and Equipment (NEL-KF-201905)+1 种基金Applied Basic Research Program of Yunnan Province, China (202101AU070154, 2019FD034)Analysis and Testing Fund of Kunming University of Science and Technology (2020 T20200006)
文摘The cognition of active sites in the Ni-based catalysts plays a vital role and remains a huge challenge in improving catalytic performance of low temperature CO_(2) dry reforming of methane(LTDRM).In this work,typical catalysts of SiO_(2) and γ-Al_(2)O_(3) supported Ni and Ni-Ce were designed and prepared.Importantly,the difference in the chemical speciations of active sites on the Ni-based catalysts is revealed by advanced characterizations and further estimates respective catalytic performance for LTDRM.Results show that larger[Ni0-]particles mixed with[Ni-O-Sin])species on the Ni/SiO_(2)(R)make CH_(4) excessive decomposition,leading to poor activity and stability.Once the Ce species is doped,however,superior activity(59.0%CH_(4) and 59.8%CO_(2) conversions),stability and high H_(2)/CO ratio(0.96)at 600℃ can be achieved on the Ni-Ce/SiO_(2)(R),in comparison with other catalysts and even reported studies.The improved performance can be ascribed to the formation of integral([Ni0_(n))]-[CeⅢ-□-CeⅢ])species on the Ni-Ce/SiO_(2)(R)catalyst,containing highly dispersed[Ni]particles and rich oxygen vacancies,which can synergistically establish a new stable balance between gasification of carbon species and CO_(2) dissocia-tion.With respect to Ni-Ce/γ-Al_(2)O_(3)(R),the Ni and Ce precursors are easily captured by extra-framework Al_(n)-OH groups and further form stable isolated([Ni0_(n))]-[Ni-O-Al_(n)])and[CeⅢ-O-Al_(n)]species.In such a case,both of them preferentially accelerate CO_(2) adsorption and dissociation,causing more car-bon deposition due to the disproportionation of superfuous CO product.This deep distinguishment of chemical speciations of active sites can guide us to further develop new efficient Ni-based catalysts for LTDRM in the future.
基金Project supported by National Natural Science Foundation of China(51204083,51374004,51104074,51174105,51306084)the Applied Basic Research Program of Yunnan Province(2012FD016)the Candidate Talents Training Fund of Yunnan Province(2012HB009)
文摘Chemical interaction of Ce-Fe mixed oxides was investigated in methane selective oxidation via methane temperature programmed reduction and methane isothermal reaction tests over Ce-Fe oxygen carriers. In methane temperature programmed reduction test, Ce-Fe oxide behaved complete oxidation at the lower temperature and selective oxidation at higher temperatures. Ce-Fe mixed oxides with the Fe content in the range of 0.1~）.5 was able to produce syngas with high selectivity in high-temperature range （800-900 ~C）, and a higher Fe amount over 0.5 seemed to depress the CO formation. In isothermal reaction, complete oxidation oc- curred at beginning following with selective oxidation later. Ce~_xFexO2~ oxygen carriers （x5_0.5） were proved to be suitable for the selective oxidation of methane. Ce-Fe mixed oxides had the well-pleasing reducibility with high oxygen releasing rate and CO selec- tivity due to the interaction between Ce and Fe species. Strong chemical interaction of Ce-Fe mixed oxides originated from both Fe＊ activated CeO2 and Ce3＋ activated iron oxides （FeOm）, and those chemical interaction greatly enhanced the oxygen mobility and selectivity.
基金both the US Army Engineer Research and Development Center,Vicksburg,MS,USA (throughout DOD contracts # W912HZ-06-C-0057 and # W912HZ-06-C-096)Ministry of Science,Education and Sports of Republic of Croatia (Project #125-1253092-1981) for funding this work
文摘The objective of the study was to investigate the presence and the activity of quantum dots nanoparticles in colored wastewaters.The special interest is devoted to the investigation of their role in the typical treatment of water or wastewater,studying their influence on the effectiveness of applied treatments methods.The standard chemical processes for water treatment and disinfection （direct UV photolysis and direct ozonation） were applied for the degradation of colored organic pollutant,reactive azo dye,in the presence/absence of CdSe/ZnS core-shells quantum dots.The obtained results indicated that investigated nanoparticles inhibit the overall efficiency of applied processes,especially in the case of direct UV photolysis,although catalytic effect might be expected in part due to the semiconductor nature of quantum dots.Such results lead to a conclusion that CdSe/ZnS nanoparticles behave as additional pollutants in the system.They should be removed from the system prior the treatment,because their presence could decrease the efficiency,i.e.,prolong the time of treatment and correspondingly increase the costs of the treatment process.
基金supported by a grant from the Romanian National Authority for Scientific Research, CNCS-UEFISCDI, project number PN-II-ID-PCE-20113-0218
文摘The electrochemical behaviours of unrecrystallized and recrystallized Ti12Mo5Ta alloys were compared with those of the unrecrystallized Ti12 Mo alloy and commercial pure titanium（cp-Ti）. Experiments were carried out using physiological 0.9% NaCl solution（pH 2.3） at 37 °C. Very low passive current densities（in order of 10-6 A/cm2） were obtained from the anodic polarization curves, indicating high resistances of all samples in acidified 0.9% Na Cl solution. Scanning electron microscopy（SEM） was employed to observe the surface morphology and all sample surfaces were identically corroded, no pitting, cracks, or other defects appeared on the sample surfaces after anodic potentiodynamic polarization tests. Equivalent circuit was used for modeling the electrochemical impedance spectroscopy（EIS） data, in order to characterize the sample surface and better understand the effect of Mo and Ta addition on the cp-Ti and the effect of recrystallization. The EIS results confirm that all titanium samples exhibit passivity in physiological 0.9% NaCl solution（pH 2.3） at open circuit potential（polarization resistance is around 105 Ω·cm2）. The corrosion resistance of these samples in physiological 0.9% NaCl solution（pH 2.3） at 37 °C is in the following order of recrystallized Ti12Mo5Ta〉 unrecrystallized Ti12Mo5Ta 〉 unrecrystallized Ti12Mo 〉 cp-Ti.
基金supported by the National Natural Science Foundation of China(42272202 and 52264001)the Yunnan Fundamental Research Projects(202201AT070144)+1 种基金the Yunnan Ten Thousand Talents Plan Young&Elite Talents Project(YNWRQNBJ-2019-164)Training Programmes of Innovation and Entrepreneurship for Undergraduates of Yunnan Province(S202210674128).
文摘In order to comprehend the applicability of microwave irradiation for recovering coalbed methane,it is necessary to evaluate the microwave irradiation-induced alterations in coals with varying levels of metamorphism.In this work,the carbon molecular sieve combined with KMnO_(4)oxidation was selected to fabricate carbon molecular sieve with diverse oxidation degrees,which can serve as model substances toward coals.Afterwards,the microwave irradiation dependences of pores,functional groups,and highpressure methane adsorption characteristics of model substances were studied.The results indicated that microwave irradiation causes rearrangement of oxygen-containing functional groups,which could block the micropores with a size of 0.40-0.60 nm in carbon molecular sieve;meanwhile,naphthalene and phenanthrene generated by macro-molecular structure pyrolysis due to microwave irradiation could block the micropores with a size of 0.70-0.90 nm.These alterations in micropore structure weaken the saturated methane adsorption capacity of oxidized carbon molecular sieve by 2.91%-23.28%,suggesting that microwave irradiation could promote methane desorption.Moreover,the increased mesopores found for oxidized carbon molecular sieve after microwave irradiation could benefit CH4 diffusion.In summary,the oxidized carbon molecular sieve can act as model substances toward coals with different ranks.Additionally,microwave irradiation is a promising technology to enhance coalbed methane recovery.
基金National Natural Science Foundation of China (Nos. 22078242 and U20A20153)Applied Basic Research Program of Yunnan Province (Nos. 202101BE070001-032 and 202101BH070002)。
文摘Fe-N-C catalysts are widely considered as promising non-precious-metal candidates for electrocatalytic oxygen reduction reaction(ORR),Yet despite their high catalytic activity through rational modulation,challenges remain in their low site density and unsatisfactory mass transfer structure.Herein,we present a structural engineering approach employing a soft-template coating strategy to fabricate a hollow and hierarchically porous N-doped carbon framework anchored with atomically dispersed Fe sites(FeNCh) as an efficient ORR catalyst.The combination of hierarchical porosity and high exterior surface area is proven crucial for exposing more active sites,which gives rise to a remarkable ORR performance with a half-wave potential of 0.902 V in 0.1 m KOH and 0.814 V in 0.1 m HClO_(4),significantly outperforming its counterpart with solid structure and dominance of micropores(FeNC-s).The mass transfer property is revealed by in-situ electrochemical impedance spectroscopy(EIS) measurement.The distribution of relaxation time(DRT) analysis is further introduced to deconvolve the kinetic and mass transport processes,which demonstrates an alleviated mass transport resistance for FeNC-h,validating the effectiveness of structural engineering.This work not only provides an effective structural engineering approach but also contributes to the comprehensive mass transfer evaluation on advanced electrocatalyst for energy conversion applications.
文摘Physicochemical, functional and digestibility analyses were done of dehydrated quail egg white to determine its possible practical applications. Quail egg white was dehydrated by air convection using one of two temperatures and times: M1 (65℃, 3.5 h), M2 (65℃, 5.0 h), M3 (70℃, 3.5 h) and M4 (70℃, 5.0 h). Lyophilized quail egg white was used as a standard. All four air-dried treatments had good protein levels (92.56% to 93.96%), with electrophoresis showing the predominant proteins to be lysozyme, ovalbumin and ovotransferin. Denaturation temperatures ranged from 81.16℃ to 83.85℃ and denaturation enthalpy values from 5.51 to 9.08 J/g. Treatments M1-4 had lower water-holding (0.90 - 2.95 g/g) and oil-holding (0.92 - 1.01 g/g) capacities than the lyophilized treatment (4.5 g/g, 1.95 g/g, respectively). Foaming capacity was pH-dependent in all five treatments, with the lowest values at alkaline pH and the highest (153% to 222%) at acid pH (pH 2). Foam stability was lowest at acid pH and highest at alkaline pH. Emulsifying activity in the air-dried treatments was highest at pH 8 (41% - 46%). Emulsion stability was pH-dependent and highest in M3 between pH 2 and 4 (96.16% to 95.74%, respectively). In the air-dried treatments, in vitro protein digestibility was as high as 83.02% (M3).
文摘The aim of this study was to evaluate the texture of corn dough as well as the nutritional quality and acceptance of corn cakes (tortillas) made either with a readymade commercial corn flour (CCF) or with a traditional way (nixtamal) both fortified with lys + tryp (L + T) or with a protein concentrate from Phaseolus lunatus added with L + T (PC + L + T). All treatments were analyzed to investigate the physical properties of the dough and tortillas as well as their physicochemical and nutritional quality. Results showed that cohesion was affected (p tortillas made with nixtamal showed no difference. Adhesion was not affected by treatments. Weight loss increased only in the fortified tortillas made with CCF (p tortillas increased with the fortification being the highest value 0.96 N. Color was not affected in tortillas made with CCF (p tortillas made with CCF and fortified with PC + L + T. Acceptance was greater for tortillas fortified with L+T alone. Protein fortification of tortillas made with either CCF or nixtamal is feasible using either L + T together or in combination with a PC from Phaseolus lunatus improving their nutritional value without negative effects on their physicochemical characteristics or acceptance.
基金funded under the Collaborative Research Initiative Grant Scheme(C-RIGS),grant number C-RIGS24-016-0022 from IIUM.
文摘This review provides a comprehensive overview of natural rubber(NR)composites,focusing on their properties,compounding aspects,and renewable practices involving natural fibre reinforcement.The properties of NR are influenced by the compounding process,which incorporates ingredients such as elastomers,vulcanizing agents,accelerators,activators,and fillers like carbon black and silica.While effective in enhancing properties,these fillers lack biodegradability,prompting the exploration of sustainable alternatives.The potential of natural fibres as renewable reinforcements in NR composites is thoroughly covered in this review,highlighting both their advan-tages,such as improved sustainability,and the challenges they present,such as compatibility with the rubber matrix.Surface treatment methods,including alkali and silane treatments,are also discussed as solutions to improve fibre-matrix adhesion and mitigate these challenges.Additionally,the review highlights the potential of oil palm empty fruit bunch(EFB)fibres as a natural fibre reinforcement.The abundance of EFB fibres and their alignment with sustainable practices make them promising substitutes for conventional fillers,contributing to valuable knowledge and supporting the broader move towards renewable reinforcement to improve sustain-ability without compromising the key properties of rubber composites.
基金Babol Noshirvani University of Technology for financially support of this project(BNUT/393054/2023)。
文摘In this study,Pebax■2533 polymer was used as the continuous phase and UiO-67 was employed as the filler to prepare mixed matrix membranes.UiO-67 is usually synthesized using two ligands:biphenyl-4,4'-dicarboxylate(bpdc)and 2,2'-bipyridine-5,5'-dicarboxylic acid(bpy).In this research,UiO-67 was synthesized not only with these two ligands but also using a mixed ligand approach(50% bpdc and 50% bpy).The synthesized UiOs were incorporated into the polymer matrix at mass percentages ranging from 0% to 2% to form the mixed matrix membranes(MMMs).Membranes containing UiO-67 with mixed ligands exhibited a greater affinity for CO_(2) compared to other membranes.Various analytical techniques,including X-ray diffraction,thermogravimetric analyzer,Fourier transform infrared spectroscope(FTIR),field emission scanning electron micro scope(FESEM),and differential scanning calorimetry,were used to analyze the properties of the prepared membranes.The FTIR spectrum confirmed all desired bands of Pebax?2533 and UiO-67 in the MMMs.The FESEM images showed that the pure Pebax membrane has a uniform structure,and the developed membranes are uniformly incorporated with the synthesized UiO-67 nanoparticles.Gas permeation measurements indicated that CO_(2) permeability and CO_(2)/CH_4 selectivity increased from 402.7 Barrer(1 Barrer=1.33×10^(-14)m^(3)(STP)·m·m^(-2)·s^(-1)·kPa^(-1))and 9.32 for the pure Pebax membrane at 1.0 MPa to 770.1 Barrer and 16.96 in the modified membrane.Additionally,the gas permeation test results demonstrated that adding functionalized porous nanofillers increases the CO_(2)separation performance.Permeability tests at different temperatures revealed that as temperature was raised,at constant pressure,CO_(2) permeability for the membrane containing the mixed ligand increased from 682.2 Barrer to 733.5 Barrer,While CO_(2)/CH_(4) selectivity decreased from 15.46 to 13.43.
基金financially supported by National Natural Science Foundation of China(22208137 and 22068022)Yunnan Fundamental Research Projects(202101BE070001-033,202401AT070825,202201BE070001007 and 202301AV070005)。
文摘Concurrent activation of lattice oxygen(O_L)and molecular oxygen(O_(2))is crucial for the efficient catalytic oxidation of biomass-derived molecules over metal oxides.Herein,we report that the introduction of ultralow-loading of Ru single atoms(0.42 wt%)into Mn_(2)O_(3)matrix(0.4%Ru-Mn_(2)O_(3))greatly boosts its catalytic activity for the aerobic oxidation of 5-hydroxymethylfurfural(HMF)to 2,5-furandicarboxylic acid(FDCA).The FDCA productivity over the 0.4%Ru-Mn_(2)O_(3)(5.4 mmol_(FDCA)g_(cat)h^(-1))is 4.9 times higher than the Mn_(2)O_(3).Especially,this FDCAproductivity is also significantly higher than that of existing Ru and Mn-based catalysts.Experimental and theoretical investigations discovered that the Ru single atom facilitated the formation of oxygen vacancy(O_(v))in the catalyst,which synergistically weakened the Mn-O bond and promoted the activation of O_L.The co-presence of Ru single atoms and O_(v)also promote the adsorption and activation of both O_(2)and HMF.Consequently,the dehydrogenation reaction energy barrier of the rate-determining step was reduced via both the O_L and chemisorbed O_(2)dehydrogenation pathways,thus boosting the catalytic oxidation reactions.
文摘Membrane fouling remains the primary economic barrier to the widespread implementation of membrane bioreactors (MBRs), despite the fact that they lead to the production of high-quality effluent. Operational conditions are critical factors influencing membrane fouling. This study aimed to investigate the simultaneous impacts of temperature and hydraulic retention time (HRT) variations on membrane fouling. Experiments were conducted at three different temperatures (18°C, 25°C, and 32°C) and HRTs (6 h, 9 h, and 15 h). The results demonstrated that increases in both temperature and HRT contributed to a reduction in membrane fouling. Additionally, a positive interaction between temperature and HRT was observed in the linear slope variation of membrane permeation, with temperature variations exerting a greater influence on membrane fouling than HRT variations. Fouling factor analysis revealed that increases in temperature and HRT led to decreased concentrations of soluble microbial products (SMP) and extracellular polymeric substances (EPS), particularly carbohydrates, in the activated sludge. Analyses of the cake layer of the membrane indicated that increasing temperature and HRT reduced EPS levels, particularly polysaccharides and proteins;altered primary protein structure;and increased the mean particle size distribution. Ultimately, these changes led to reductions in both reversible and irreversible hydraulic resistances. This study highlights the importance of optimizing operational parameters such as temperature and HRT to enhance membrane performance and treatment efficiency in MBR systems while mitigating fouling.
基金supported by National Natural Science Foundation of China(U21A20316).
文摘Magnetization roasting technology is one of the most representative ways to improve the magnetic separation efficiency and iron recovery of refractory weakly magnetic iron ores.However,utilization of CO-rich or H_(2)-rich gas of strong reducibility as reducing agent for magnetization roasting would lead to over-reduction of Fe_(2)O_(3) in the ore to non-magnetic FeO,which makes the magnetism of the roasted ore be lower than its maximum,and hence leads to a lower iron recovery than expected.To explore the possibility of using CH_(4) as reducing agent for controllable reduction of Fe_(2)O_(3) in iron ores to selectively forming magnetic Fe_(3)O_(4),i.e.,for maximizing the magnetism of the reduced ore for efficient iron separation and recovery,a series of fluidized bed reduction tests in CH_(4) were carried out on two iron ores of 55%and 33%iron at different temperatures for different periods of time,and the resultant reduced ore particles were magnetically separated for recovery of iron concentrate.XRD and ICP analyses were performed on all recovered iron concentrates to identify the crystal forms of their iron species and to quantify their iron contents.The results have shown that the controllable reduction by CH_(4) of Fe_(2)O_(3) in the iron ores to strongly magnetic Fe_(3)O_(4) can be realized by controlling the reduction temperature and time condition applied.The resultant concentrates can be fully recovered by magnetic separation in a weak magnetic field of 60 kA/m to attain a maximum iron recovery of 98% for the high-grade ore and that of 65% for the low-grade ore.Besides,the results have also shown that the most critical factor affecting the controllability of the ore reduction process and the selectivity to the generation of magnetic Fe_(3)O_(4)-containing particles is the reduction temperature,and that the upper temperature threshold for the controllable reduction and selective generation of strongly magnetic iron concentrate is about 650℃.
基金supported by a grant from the Ministry of Research, Innovation and Digitization, UEFISCDI, Grant Nos. PN-IIIP2-2.1-PED-2021-1890, PN-IV-P6-6.3-SOL-2024-2-0254 and PNIV-P7-7.1-PTE-2024-0517, within PNCDI Ⅳ.
文摘This study represents an important step forward in the domain of additive manufacturing of energetic materials.It presents the successful formulation and fabrication by 3D printing of gun propellants using Fused Deposition Modeling(FDM)technology,highlighting the immense potential of this innovative approach.The use of FDM additive manufacturing technology to print gun propellants is a significant advancement due to its novel application in this field,which has not been previously reported.Through this study,the potential of FDM 3D-printing in the production of high-performance energetic composites is demonstrated,and also a new standard for manufacturability in this field can be established.The thermoplastic composites developed in this study are characterized by a notably high energetic solids content,comprising 70%hexogen(RDX)and 10%nitrocellulose(NC),which surpasses the conventional limit of 60%energetic solids typically achieved in stereolithography and light-curing 3D printing methods.The primary objective of the study was to optimize the formulation,enhance performance,and establish an equilibrium between printability and propellant efficacy.Among the three energetic for-mulations developed for 3D printing feedstock,only two were suitable for printing via the FDM tech-nique.Notably,the formulation consisting of 70%RDX,10%NC,and 20%polycaprolactone(PCL)emerged as the most advantageous option for gun propellants,owing to its exceptional processability,ease of printability,and high energetic performance.
基金supported by the National Natural Science Foundation of China (Nos.52260013,51968034,and 21876071)the Yunnan Major Scientific and Technological Projects (No.202202AG050005).
文摘In this study,non-thermal plasma(NTP)was employed to modify the Cu/TiO_(2)adsorbent to efficiently purify H_(2)S in low-temperature and micro-oxygen environments.The effects of Cu loading amounts and atmospheres of NTP treatment on the adsorption-oxidation performance of the adsorbents were investigated.The NTP modification successfully boosted the H_(2)S removal capacity to varying degrees,and the optimized adsorbent treated by air plasma(Cu/TiO_(2)-Air)attained the best H_(2)S breakthrough capacity of 113.29 mg H_(2)S/gadsorbent,which was almost 5 times higher than that of the adsorbent without NTP modification.Further studies demonstrated that the superior performance of Cu/TiO_(2)-Air was attributed to increased mesoporous volume,more exposure of active sites(CuO)and functional groups(amino groups and hydroxyl groups),enhanced Ti-O-Cu interaction,and the favorable ratio of active oxygen species.Additionally,the X-ray diffraction(XRD)and X-ray photoelectron spectroscopy(XPS)results indicated the main reason for the deactivationwas the consumption of the active components(CuO)and the agglomeration of reaction products(CuS and SO_(4)^(2−))occupying the active sites on the surface and the inner pores of the adsorbents.
基金supported by the Istanbul Technical University-Scientific Research Projects(ITUBAP)with project number of 45964Additional financial support was granted by the Scientific and Technological Research Council of Turkey(TUBITAK)under the 2218 Domestic Post-Doctoral Research Fellowship Program(Project No.118C574).
文摘Interfacial compatibilization is essential to generate compatible blend structures with synergistically enhanced properties.However,the effect of molecular structure on the reactivity of compatibilizers is not properly known.This study investigates the compatibilization effect of multifunctional,epoxy-based Joncryl chain extender in blends of polylactide(PLA)and polybutylene adipate-co-terephthalate(PBAT)using PLA with varying D-lactide contents and molecular weights.These PLAs were high molecular weight amorphous PLA(aPLA)with D-content of 12 mol%and semi-crystalline PLA(scPLA)grades with D-contents below 1.5 mol%at both high(h)and low(l)molecular weights.The reactivity of Joncryl was assessed with each individual neat polymer,and its compatibilization effectwas examined in blends at aweight ratio of 75 wt/25wt using small amplitude oscillatory shear(SAOS)rheological analysis.Differential scanning calorimetry(DSC),dynamic mechanical analysis(DMA),tensile and impact tests,as well as scanning electron microscopy(SEM)observations,were conducted to characterize the blends.The addition of Joncryl resulted in remarkable improvements rheological behavior of all neat polymers and noticeably refined PBAT droplets in all blends,particularly in aPLA/PBAT and scPLA(l)/PBAT.The ductility,toughness and impact strength of these blends were significantly enhanced,while their tensile strength and modulus also showed slight improvements.Although the addition of Joncryl retarded the crystallization of the scPLA samples,the scPLA(h)/PBAT blend with Joncryl exhibited the highest thermomechanical performance over a wide temperature range.This was attributed to the higher crystallinity of scPLA(h),which,even in the presence of Joncryl,provided high thermal stability.
基金Ho Chi Minh City University of Technology(HCMUT),VNU-HCM,for supporting this study.
文摘This study focuses on the preparation,and optimization of the nanoemulsions coorporating with pumpkin seed oil,grape seed oil,and grapefruit essential oil using the phase inversion temperature(PIT)technique.The research investigated the impact of surfactant types and concentrations on critical nanoemulsion properties,including droplet size,polydispersity index(PDI),and zeta potential.Using a Box-Behnken Design(BBD)model,the formulation was optimized containing 6.0%plant oils,10.0%Tween 80,2.0%Span 80,and 1.0%lecithin to achieve nano-sized droplets(33.52 nm),with a low PDI(0.205),and a stable zeta potential(15.49 mV).The antioxidant activity,was evaluated through 2,2-diphenyl-1-picrylhydrazyl(DPPH)radical scavenging assays,demonstrating its outstanding efficacy.And the optimized nanoemulsion showed a radical-scavenging capacity exceeding 2250μg ascorbic acid equivalents/g,significantly outperforming non-nanoemulsified oils.Stability testing under various environmental conditions highlighted exceptional robustness,with refrigerated samples maintaining structural integrity,minimal particle size growth,and consistent physicochemical properties over a 30-day storage period.The results suggest that the plant oil-based nanoemulsions exhibit strong antioxidant potential,offering a promising natural treatment for their application in cosmeceutical and therapeutic formulations.
