Infuences of Different Admixtures on the Drying Shrinkage Characteristics of Metakaolin-based Geopolymer Mortar

To investigate the influences of different admixtures on the drying shrinkage of polymer mortar in a metakaolin base,the experiments of VAE(vinyl acetate ethylene copolymer),APAM(anionic polyacrylamide)and CPAM(cationic polyacrylamide)on the drying shrinkage properties of geopolymer mortar were designed under normal temperature curing conditions.An SP-175 mortar shrinkage dilatometer was introduced to measure the dry shrinkage of geopolymer mortar.Meanwhile,the drying shrinkage properties of geopolymer mortar are exhibited by the parameters of water loss rate,drying shrinkage rate,drying shrinkage strain and drying shrinkage coefficient.The experimental data are further fitted to obtain the prediction model of dry shrinkage of geopolymer mortar,which can better reflect the relationship between dry shrinkage rate and time.Finally,the experimental results demonstrate that the dry shrinkage of geopolymer mortar can be significantly increased by adding 4%VAE admixture,meanwhile under the condition that the polymer film formed by VAE reaction can strengthen and toughen the mortar.2.5%APAM admixture and 1.5%CPAM admixture can enhance the dry shrinkage performance of geopolymer mortar in a certain range.

Molecular dynamics simulations on the wet/dry self-latching and electric fields triggered wet/dry transitions between nanosheets:A non-volatile memory nanostructure

We design a nanostructure composing of two nanoscale graphene sheets parallelly immersed in water.Using molecular dynamics simulations,we demonstrate that the wet/dry state between the graphene sheets can be self-latched;moreover,the wet→dry/dry→wet transition takes place when applying an external electric field perpendicular/parallel to the graphene sheets(E;/E;).This structure works like a flash memory device(a non-volatile memory):the stored information(wet and dry states)of the system can be kept spontaneously,and can also be rewritten by external electric fields.On the one hand,when the distance between the two nanosheets is close to a certain distance,the free energy barriers for the transitions dry→wet and wet→dry can be quite large.As a result,the wet and dry states are self-latched.On the other hand,an E;and an E;will respectively increase and decrease the free energy of the water located in-between the two nanosheets.Consequently,the wet→dry and dry→wet transitions are observed.Our results may be useful for designing novel information memory devices.

Synthesis and electrochemical performance of micro-nano structured Li Fe1-xMnxPO4/C(0≤x≤0.05)cathode for lithium-ion batteries

Micro-nano structured Li Fe（1-x）MnxPO4/C（0≤x≤0.05）cathodes were prepared by spray drying,followed by calcination at 700°C.The spherical Li Fe（1-x）MnxPO4/C（0≤x≤0.05）particles with the size of 0.5 to5.0μm are composed of lots of nanoparticles of 20 to 30 nm,and have the well-developed interconnected pore structure.In contrast,when Mn doping content is 3 mol%（x=0.03）,the Li Fe（0.97）Mn（0.03）PO4/C demonstrates maximum specific surface area of 31.30 m^2/g,more uniform pore size and relatively better electrochemical performance.The initial discharge capacities are 161.59,157.04 and 153.13 m Ah/g at a discharge rate of 0.2,0.5 and 1 C,respectively.Meanwhile,the discharge capacity retentions are～100%after 120 cycles.The improved electrochemical performance should be attributed to higher specific surface,smaller polarization voltage,and a high Li~＋diffusion rate due to the micro-nano porous structure and lattice expansion produced by Mn doping.