thermal stability

摘要： Hydrogels have been widely applied in agricultural drought-resistance,pollution regulation,drug delivery and so on.Acrylamide(AM)is usually used as raw material to synthesize acrylamide hydrogels.However,inherently low mechanical strength greatly limits their applications in some special areas.Therefore,it is necessary to choose suitable functional monomers to optimize acrylamide hydrogels and improve their mechanical performances.In this paper,a novel acrylamide monomer modified by rosin was synthesized,and then polyacrylamide/rosinbased acrylamide(RAM)composite hydrogels were prepared via free radical polymerization using potassium persulfate as initiator,N,N′-methylene-bisacrylamide(MBA)as a crosslinker.The influence of RAM monomer was investigated in detail.The chemical structure,pore structure,swelling properties,thermal performances and mechanical properties of composite hydrogels were characterized by Fourier Transform Infrared spectrometer(FT-IR),thermogravimetric analysis(TG),scanning electron microscope(SEM),and universal testing,respectively.The results showed that the thermal stability and mechanical property of RAM hydrogels were improved significantly.The compressive strength of RAM hydrogels was increased to 3.5 times than that of AM hydrogels,and the tensile strength was 5.1 times compared with AM hydrogels as well.Moreover,RAM hydrogels exhibited a faster initial swelling rate due to the new pore structure formed after introducing the RAM monomer.

摘要： The thermal and dimensional stability of epoxy resin(EP)in-situ modified by cyanate ester(CE)and polydimethylsiloxane(PDMS)are investigated by means of experiments and numerical simulation.Thermal gravimetric analysis(TGA)and differential scanning calorimeter(DSC)are used to analyze the heat resistance of the modified EP.The dimensional stability is characterized by the volume shrinkage of the series PDMS/CE/EP obtained by the density method.The chemical structure of the PDMS/CE/EP is analyzed by Fourier transform infrared spectroscopy(FTIR).The results of TGA and DSC indicate that the thermal stability of PDMS/CE/EP decreases firstly and then increases with the increase in the amount of CE.The addition of PDMS shows a slight effect on the thermal stability.The 40%CE makes the blending system exhibit the lowest initial decomposition temperature,which reduces by 15.5%and 40.8%compared with pure EP and CE,respectively.The FTIR results suggested that the influence of CE on the thermal stability of the modified EP is mainly ascribed to the generation of oxazolidinone ring with low thermal stability and the increase in the triazine ring with high thermal stability.The volume shrinkage measurement results show that the introduction of CE and PDMS are both beneficial to the improvement of the dimensional stability of the blending systems.The in-situ addition of 80%CE shows the lowest volume shrinkage of6.11%.The thermal stress distribution of PDMS/CE/EP generated during the solidification process is simulated by the finite element analysis.The results suggested that the introduction of 80%CE into EP results in the lowest thermal stress in the blending system,which indicates that the system has the lowest volume shrinkage,which agrees well with the experimental results.

摘要： Owing to the increasing energy demands and the environmental constraints,the need for bio-based materials has been on the rise due to their variety of favorable properties like biocompatibility,cost-effectiveness,large specific surface area,high porosity,and non-toxicity.Thermal stability and mechanical strength of aerogels are highly dependent on their micro-porous structures.A three-dimensional structure based on cellulose nanofiber/chitosan(CNF/CS)aerogels was built using two different freezing methodologies,namely random freezing,and unidirectional freezing techniques,by changing mold shapes.The unidirectional aerogels ultimately resulted in high-temperature stability and mechanical strength.The results show that the unidirectional CNF/CS(u-CNF/CS)aerogels contain controlled micro porous orientation relative to random-CNF/CS(r-CNF/CS)aerogels with the disordered porous distribution.The high-temperature stability with an increase of glass transition temperature T_(g) from 275°C(CNF)to 283°C(CNF/CS),the ultra-low thermal conductivity of 0.030 W/(m·K),and mechanical robustness of u-CNF/CS aerogels make them quite favorable for practical applications.

摘要： A once overlooked source of electrolyte degradation incurred by dissolved manganese(Ⅱ)species in lithium-ion batteries has been identified recently.In order to deactivate the catalytic activity of such manganese(II)ion,1-aza-12-crown-4-ether(A12C4)with cavity size well matched manganese(Ⅱ)ion is used in this work as electrolyte additive.Theoretical and experimental results show that stable complex forms between A12C4 and manganese(II)ions in the electrolyte,which does not affect the solvation of Li ions.The strong binding effect of A12C4 additive reduces the charge density of manganese(II)ion and inhibits its destruction of the PF_(6)^(-)
structure in the electrolyte,leading to greatly improved thermal stability of manganese(II)ions-containing electrolyte.In addition to bulk electrolyte,A12C4 additive also shows capability in preventing Mn^(2+) from degrading SEI on graphite surface.Such bulk and interphasial stability introduced by A12C4 leads to significantly improved cycling performance of LIBs.

摘要： The magnesium alloys are the next-generation lightweight metal materials;however, the production of the complex shape components of thermo-mechanical processed magnesium alloys is very limited in comparison to their die-casted counterparts. Both high strain rate and low-temperature processing are required to save time and cost for the project. Uniaxial tensile testing has been vastly used for determining the plasticity of magnesium alloys at elevated temperatures. Therefore, this review article sheds light on superplastic behaviors under the uniaxial tensile loading of different magnesium alloys. This review also emphasizes low and high-temperature superplasticity, high strain rate superplasticity, deformation mechanism, thermal stability, texture evaluation, and fracture mechanism of extruded/rolled and severe plastic deformed magnesium alloys. At the end of the review, some technical issues have been addressed which can be beneficial for further enhancement in the superplasticity of magnesium alloys.

摘要： 3D printing is nowadays used for many applications far beyond pure rapid prototyping.As tools to prepare custom-made objects which may be highly complex,different 3D printing techniques have emerged into areas of application where the mechanical,thermal,optical and other properties have to meet high requirements.Amongst them,applications for space,e.g.for microsatellites,make extreme demands regarding the stability under high temperatures.Nevertheless,polymeric 3D printed materials have several advantages for space application in comparison with metal objects.Here we thus investigate the impact of temperatures up to 85◦C and 185◦C,respectively,on typical 3D printing materials for fused deposition modeling or stereolithography(SLA)with inexpensive 3D printers.The materials are found to differ strongly in terms of mechanical properties and dimensional stability after the treatment at a higher temperature,with SLA resins and co-polyester showing the best dimensional stability,while acrylonitrile–butadiene–styrene and SLA resin after long UV post-treatment has the best mechanical properties.

摘要： High applied thermal-stability and superior structural property for activated carbon adsorbent are extremely promising,which also is the determining short slab in volatile organic compounds(VOCs)adsorption applications.Herein,we develop the outstanding engineering carbon adsorbents from waste shaddock peel which affords greatly-enhanced thermal-stability and super structural property(S_(Lang)=4962.6 m2·g^(-1),Vmicro=1.67 cm^(3)·g^(-1)).Such character endows the obtained adsorbent with ultrahigh adsorption capture performance of VOCs specific to benzene(16.58 mmol·g^(-1))and toluene(15.50 mmol·g^(-1),far beyond traditional zeolite and activated carbon even MOFs materials.The structural expression characters were accurately correlated with excellent adsorption efficiency of VOCs by studying synthetic factor-controlling comparative samples.Ulteriorly,adsorption selectivity prediction at different relative humidity was demonstrated through DIH(difference of the isosteric heats),exceedingly highlighting great superiority(nearly sixfold)in selective adsorption of toluene compared to volatile benzene.Our findings provide the possibility for practical industrial application and fabrication of waste biomass-derived outstanding biochar adsorbent in the environmental treatment of threatening VOCs pollutants.

摘要： Benzoxazines have attracted wide attention from academics all over the world because of their unique properties.However,most of the production and preparation of benzoxazine resins depends on petroleum resources now,especially bisphenol A-based benzoxazine.Therefore,owing to the environmental impacts,the development of bio-based benzoxazines is gaining more and more interest to substitute petroleum-based benzoxazines.Similar to petroleum-based benzoxazines,most of bio-based benzoxazines suffer from flammability.Thus,it is necessary to endow bio-based benzoxazines with outstanding flame retardancy.The purpose of this review is to summarize the latest advance in flame retardant bio-based benzoxazines.First,three methods of the synthesis of bio-based benzoxazines are introduced briefly.Furthermore,the curing mechanism of benzoxazine and the effect of branched chains on the curing behavior are also discussed and summarized.Subsequently,this review focuses on fully bio-based benzoxazines,partly bio-based benzoxazines,and bio-based benzoxazine composite materials in terms of flame retardancy as well as thermal stability and some other special properties.Finally,we give a brief comment on the challenges and prospects of the future development of flame retardant bio-based benzoxazines.

摘要： In comparison to widely adopted bulk heterojunction(BHJ)structures for organic solar cells(OSC),exploiting the sequential deposition to form planar heterojunction(PHJ)structures enables to realize the favorable vertical phase separation to facilitate charge extraction and reduce charge recombination in OSCs.However,effective tunings on the power conversion efficiency(PCE)in PHJ-OSCs are still restrained by the currently available methods.Based on a polymeric donor PBDBT-2 F(PBDBT=Poly[[4,8-bis[5-(2-ethylhexyl)-4-fluoro-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl]-2,5-thiophenediyl[5,7-bis(2-ethylhexyl)-4,8-dioxo-4 H,8 H-benzo[1,2-c:4,5-c′]dithiophene-1,3-diyl]-2,5-thiophenediyl])and a non-fullerene(NF)acceptor Y6,we proposed a strategy to improve the properties of photovoltaic performances in PHJ-based OSCs through dilute dispersions of the PBDBT-2 F donor into the acceptor-dominant phase with the sequential film deposition.With the control of donor dispersions,the charge transport balance in the PHJ-OSCs is improved,leading to the expedited photocarrier sweep-out with reduced bimolecular charge recombination.As a result,a PCE of 15.4%is achieved in the PHJ-OSCs.Importantly,the PHJ solar cells with donor dispersions exhibit better thermal stability than corresponding BHJ devices,which is related to the better film morphology robustness and less affected charge sweep-out during the thermal aging.

摘要： The effects of tempering holding time at 700°Con the morphology,mechanical properties,and behavior of nanoparticles in Ti-Mo ferritic steel with different Mo contents were analyzed using scanning electron microscopy and transmission electron microscopy.The equilibrium solid solution amounts of Mo,Ti,and C in ferritic steel at various temperatures were calculated,and changes in the sizes of nanoparticles over time at different Mo contents were analyzed.The experimental results and theoretical calculations were in good agreement with each other and showed that the size of nanoparticles in middle Mo content nano-ferrite(MNF)steel changed the least during aging.High Mo contents inhibited the maturation and growth of nanoparticles,but no obvious inhibitory effect was observed when the Mo content exceeded 0.37wt%.The tensile strength and yield strength continuously decreased with the tempering time.Analysis of the strengthening and toughening mechanisms showed that the different mechanical properties among the three different Mo content experiment steels were mainly determined by grain refinement strengthening(the difference range was 30-40 MPa)and precipitation strengthening(the difference range was 78-127 MPa).MNF steel displayed an ideal chemical ratio and the highest thermodynamic stability,whereas low Mo content nano-ferrite(LNF)steel and high Mo content nano-ferrite(HNF)steel displayed relatively similar thermodynamic stabilities.