Influence of Solution Temperature on Microstructure and Mechanical Properties of Directionally Solidified Superalloy DZ22

The microstructure changed markedly with increasing solution temperature, i.e eutectic γ' phases and coarse primary γ' phase are redissolved continuously into matrix, which was finished at 1250-1260℃, and more and finer γ' phases are reprecipitated. The grain boundary morphology changed gradually to 'fine line' form. The dendritic segregation of elements decreased. With raising solution temperature the longitudinal stress-rupture life at high and intermediate temperature were enhanced, but the transversal stress-rupture life at intermediate temperature decreased obviously. The incipient melting temperature of DZ22 alloy was measured to be 1230-1240℃ and may be increased by homogenization at 1150℃. In this paper the principle of determining solution temperature of DS alloys was discussed. It was suggested that the solution temperature of alloy DZ22 selected at 1200-1210℃ is appropri- ate.

Effect of the tumescent infiltration solution temperature on body temperature

Objective To evaluate the effect of tumescent infiltration solution temperature on core body temperatureafter liposuction.Methods 15 healthy female subjects were randomly divided into 2 groups to receive tumescent infiltration

Solvation of halogen ions in aqueous solutions at 500 K–600 K under 100 atm

Structural properties of the pure water and halogen solutions at high temperatures and pressures are studied by using the molecular dynamics simulations and quantum molecular simulations. The related characters are calculated as functions of temperature and pressure. The results show that the hydrogen bonded networks become looser as temperature increases,with the collapse of the traditional tetrahedral structure. It is similar to the concentration-dependent collapse in the Na Cl solutions. However, adding other halogen elements has no further effects on the already weakly bonded water molecules.At the phase changing points, the process of hydration is evident for the bigger ions, so that the bigger the ion is, the smaller a cluster is formed.

Evolution laws of microstructures and mechanical properties during heat treatments for near-αhigh-temperature titanium alloys

Evolution laws of microstructures,mechanical properties,and fractographs after different solution temperatures were investigated through various analysis methods.With the increasing solution temperatures,contents of the primaryαphase decreased,and contents of transformedβstructures increased.Lamellarαgrains dominated the characteristics of transformedβstructures,and widths of secondaryαlamellas increased monotonously.For as-forged alloy,large silicides with equiaxed and rod-like morphologies,and nano-scale silicides were found.Silicides with large sizes might be(Ti,Zr,Nb)_(5)Si_(3) and(Ti,Zr,Nb)_(6)Si_(3).Rod-like silicides with small sizes precipitated in retainedβphase,exhibiting near 45°angles withα/βboundaries.Retainedβphases in as-heat treated alloys were incontinuous.980STA exhibited an excellent combination of room temperature(RT)and 650°C mechanical properties.Characteristics of fracture surfaces largely depended on the evolutions of microstructures.Meanwhile,silicides promoted the formation of mico-voids.

Salt Effect on the Phase Transition Behavior of Thermo-sensitive Polyamide

Phase transition behavior and influence of ions on the thermo-sensitive polyamide with polyethylene glycol as the main chain were studied in detail. By measuring the light transmission rates of polymer solutions, the change of its lower critical solution temperature （LCST） in the salt solution was investigated. It was found that a reversible phase transition of the polyamide occurred at the LCST and finished in a narrow temperature range. The LCST was associated with species of ions in salt solution. Anions had a great impact on the phase transition performance of the thermo-sensitive polyamide, while the cations had a slight influence on the phase transition. Different anions had different coagulation ability to ‘salt-out＇ the polyamide. The order was： CO2-3〉SiO2-3〉HPO2-4〉OH-〉Cl-〉HCO3-〉HSOa-〉NO2-〉NO3-.

Synthesis and Properties of Poly (N-isopropylacrylamide) and Poly (N-isopropylacrylamide-co-acrylamide) Hydrogels

The thermosensitive poly （ N-isopropylacrylamide ） （PNIPAAm） and poly （N-isopropylacrylamide-co-acrylamide） [ poly （NIPAAm-co-AAm） ] hydrogels with different acrylamide molar percentage are prepared by radiation polymerization using Co^60 γ-ray. Their swelling equilibrium data in the media of deionized water, NaCl aqueous solutions and different pH buffer solutions are determined. It appears that lower critical solution temperature （LCST） of the hydrogels will drop with the increase of ionic strength and increase with the rising of acrylamide content, A semi-empirical formula is set up with the experimental results. Moreover, it also indicates that this copolymer is pH-sensitive, which is similar to the homopolymer of PNIPAAm.

MOF(ZM)/Potassium Citrate-Derived Composite Porous Carbon and Its Electrochemical Properties

Metal-organic frameworks are compounds with a reticulated skeletal structure formed by chemically bonding inorganic and organic units that are widely used in many fields, such as photocatalysis, gas separation and energy storage, because of their unique structures. In this paper, we prepared a metal-organic framework [(μ2-2-methylimidazolyl)12-Zn(ii)6-H18O10]n(ZM) with well-developed pores and high specific surface area of MOFs by the solution method. And MOF-derived porous carbon was prepared by the direct charring method in an argon atmosphere using a mixture of ZM, ZM and potassium citrate as carbon precursors. Characterization analysis revealed that the maximum specific surface area of ZMPC-800-1:15 was 2014.97 m2⋅g−1, and the pore size structure was mainly mesoporous. At a current density of 1.0 A⋅g−1 the specific capacitance of ZMC-800 and ZMPC-800-1:15 was 121.3 F⋅g−1 and 226.6 F⋅g−1, respectively, with a substantial increase of 86.8%. The specific capacitance of ZMPC-800-1:15 decays to 168.8 F⋅g−1, with a decay rate of 25.5%, when the current density increases to 10.0 A⋅g−1. After 5000 constant current charge/ discharge cycles, the capacitance retention rate was still 96.41%. These results prove that the application of MOF-derived carbon materials in future supercapacitors is very promising.

Visualizing phase transition of upper critical solution temperature (UCST) polymers with AIE

The stimuli-responsive polymers with upper critical solution temperatures(UCST) are highly attractive for drug delivery applications. However, the phase transition process of UCST polymer is usually characterized by turbidity measurement and electron microscopy, which are significantly restricted by low sensitivity and static observation. In contrary, the fluorescence technique has significant advantages in terms of high sensitivity, easy operation, and dynamic observation. However, the conventional fluorophores suffer from the drawbacks of aggregation-caused quenching(ACQ) after being encapsulated by UCST polymers, which are not suitable for direct visualization of the phase transition process. To tackle this challenge, we herein developed a series of UCST polymers based on polyacrylamides decorated with bile acid and aggregation-induced emission(AIE)-active tetraphenylethene(TPE) groups, which can be used for direct fluorescence monitoring of the phase transition process. Moreover, the AIE-active UCST polymers can serve as drug carriers, which can not only monitor the drug release process under thermal stimuli, but also verify the drug release by fluorescence recovery after thermal stimuli. It is expected that the AIE-active UCST polymers with self-monitoring ability are promising for biomedical applications.

Polymer Vesicles with Upper Critical Solution Temperature for Near-infrared Light-triggered Transdermal Delivery of Metformin in Diabetic Rats

Near-infrared light(NIR)triggered transdermal drug delivery systems are of great interest due to their on-demand drug release,which enable to enhance drug treatment efficiency as well as reduce side effect.Herein,a NIR-triggered microneedle(MN)patch array has been fabricated through depositing the photothermal conversion agent and anti-diabetic drug-loaded polymer vesicles with upper critical solution temperature(UCST)into dissolvable polymer matrix.The UCST-type polymer has a clearing point temperature of 41℃ and the drug-loaded polymer vesicles present excellent NIR-triggered and temperature responsive drug release behavior in vitro due to the disassociation of polymer vesicles upon NIR irradiation.After applying MNs to diabetic rats,significant hypoglycemic effect is achieved upon interval NIR irradiation and the blood glucose concentration can decrease to normal state for several hours,which enables to achieve the goal of on-demand drug release.This work suggests that the NIR-triggered MN drug release device has a potential application in the treatment of diabetes,especially for those requiring an active drug release manner.

Control of Secondary Phases by Solution Treatment in a N-Alloyed High-Mn Cryogenic Steel

The secondary phases of the steels have significant effects on the microstructure and mechanical properties, making controlling these secondary phases important. The control of MnS inclusions and A1N precipitates in a N-alloyed high-Mn twin-induced plastic cryogenic steel via solution treatment was investigated with several different techniques including microstructural characterization, 298 K tensile testing, and 77 K impact testing. The solutionizing temperature （ST） increased from 1323 to 1573 K, where the elongated MnS inclusions and large-sized AlN precipitates became spheroidized and dissolved. The aspect ratio of the MnS inclusions decreased as the ST increased and the number density increased. The impact toughness of the steels showed anisotropy and low impact energy values, due to the elongated MnS inclusions and large-sized AIN precipitates. The anisotropy was eliminated by spheroidizing the MnS inclusions. The impact energy was improved by dissolving the large-sized AlN precipitates during the solution treatment. The austenite grain size increased when the dissolution of the AlN precipitate increased, but the effect of the grain size on the yield strength, toughness, and the strength--ductility balance was weak.

Supramolecular control over thermo-responsive systems with lower critical solution temperature behavior

Lower critical solution temperature(LCST)is the critical temperature below which the solution is miscible for all compositions and above which the solution becomes a suspension.The study of LCST properties has become a central research topic due to its profound impact on the applications of stimuli-responsive materials.Inspired by the marriage between materials science and supramolecular chemistry,the introduction of supramolecular pairs and interactions into polymeric LCST systems is increasingly practiced.Especially,supramolecular interactions provide precise control over LCST behavior in both water and organic solvents.Furthermore,supramolecular interactions not only control or adjust LCST behavior(supramolecular interaction controlled LCST),but also induce LCST phase behavior in species lack of thermo-sensitive properties(supramolecular interaction induced LCST).In this review,we summarize the applications of supramolecular interactions in LCST systems.By examining the relationship between supramolecular interactions and LCST changes,we further discuss the differences between supramolecular interaction controlled LCST and supramolecular interaction induced LCST.We hope this review will give our readers a snapshot on how the supramolecular interactions influence the LCST behavior in various systems,and benefit them with different applications.

Temperature dependence of circular DNA topological states and a solution to a single molecular experiment problem

Circular double stranded DNA has different topological states which are defined by their linking numbers. Equilibrium distribution of linking numbers can be obtained by closing

Temperature/pH dual-responsive reversible morphology evolution of block copolymer microparticles under three-dimensional confinement

Development of block copolymer(BCP)microparticles with switchable morphology in response to external stimuli is important for exploiting new intelligent materials.In this work,thermo/p H dual-responsive nanoparticles(NPs)were employed as a cosurfactant to modulate the self-assembly morphology of polystyrene-b-poly(2-vinylpyridine)(PS-b-P2VP)microparticles within confined emulsion droplets.The co-surfactant was synthesized by grafting poly(acrylic acid)-b-poly(N-isopropylacrylamide)onto the surface of Fe3O4NP.The introduction of the dual-responsive co-surfactant enabled thermo/p H dual-responsive reversible morphology transition of the PS-b-P2VP microparticles by tailoring the hydrophobicity and interfacial affinity of the cosurfactant.By using this strategy,the thermo-inert PS-b-P2VP self-assembled into pupa-like microparticles at T=10℃ and p H7.5,which could transform into tulip-like microparticles when T was increased to 50℃.When the p H value was increased to 11,the pupa-like particles turned into onion-like microparticles although the PS-b-P2VP was inert to alkali.However,the pupa-like microparticles remained unchanged when both T and p H were simultaneously increased.The PAA-b-PNIPAM-grafted Fe3O4NP surfactants showed obvious advantages over the linear PAA-b-PNIPAM surfactants in modulating the morphology transition,since the linear PAA-b-PNIPAM could not induce the reversible shape transition of microparticles.Our work provides an efficient strategy to achieve reversible shape transformation of BCP microparticles while the internal phase structure is preserved,which may be utilized to switch the structural color properties of BCP microparticles.

Room-temperature synthesis of layered open framework cathode for sodium-ion batteries

The synthesis of active electrode materials at room temperature is one of the effective strategies to reduce the fabrication cost of sodium ion batteries(SIBs).Herein,a layered material(Na_(2)[(VO)_(2)(HPO_(4))_(2)C_(2)O_(4)]·2H_(2)O,abbreviated as NVPC followingly)with open-framework structures has been successfully prepared at room temperature under ambient conditions and is evaluated as a cathode for SIBs.It is revealed that NVPC cathode can deliver a maximum reversible capacity of ca.70 mAh/g at 10 mA/g,and exhibit superior rate capability and cycling performance:at 50 mA/g,maximum reversible capacity ca.50 m Ah/g with capacity retention of 88.4%over 250 cycles corresponds to only 0.046%capacity decay per cycle;at 100 mA/g,a maximum reversible capacity of 35 mAh/g with capacity retention of60.9%over 500 cycles.This study demonstrates a practical example of a low-cost synthesis of the cathode materials for SIBs.At the same time,the systematic electrochemical research results also show promising prospects for long lifespan low-cost SIBs.

Precipitation kinetics of complex precipitate in multicomponent systems

A kinetic model based on the classical nucleation and growth theory has been proposed to predict the precipitation behavior of complex precipitate. The method for calculating absolute solution temperature, which is an important guidance for determining solution treatment temperature, is also proposed based on thermodynamic model. In the model, nucleation of the second phase is assumed to be controlled by the effective diffusion, which involves the bulk diffusion and dislocation pipe diffusion, and growth is controlled by the bulk diffusion of forming elements. The interfacial energy of complex precipitate is calculated by the linear interpolation method, and the effects of alloying elements on precipitation behavior are manifested using weighted means of their diffusivities and concentration. The predictions were compared with the experimental measurements, and a good agreement was obtained.

Synthesis of a Kind of Temperature-responsive Cell Culture Surface for Corneal Sheet

In this study, acrylic acid （AA） and 4-azidoaniline were used to modify poly （N-isopropylacrylamide） （NIPAAm） in order to fabricate temperature-responsive surface for corneal epithelia cell adhesion and detachment. First, NIPAAm was copolymerized with acrylic acid. Then, the copolymer was coupled with azidoaniline to synthesize AzPhPIA, derivative of p（NIPAAm-co-AA）, which possesses both thermo- and photo-sensitivities. Second, the synthesized copolymer was characterized by high performance liquid chromatography （HPLC）, Fourier transform infrared （FTIR） and a CHN analyzer. The thermo-sensitivity was characterized by temperature reducing experiment, contact angle measurement and low critical solution temperature （LCST） testing. Third, the derivatized copolymer was immobilized by photolithography on a polystyrene plate, and then the surface characterization of AzPhPIA-coated polystyrene plate （PSt） was measured by electron spectroscopy for chemical analysis （ESCA）. The thermo-sensitivity and cytocompatibility of the AzPhPIA-coated PSt were investigated by corneal epithelial cells culture. The results revealed that the AzPhPIA-coated PSt exhibited good cytocompatibility and cell detachability when temperature decreased.

Controlling the gelation temperature of biomimetic polyisocyanides

Thermosensitive polymers show an entropy-driven transition from a well-solvated to a poorly solvated polymer chain, resulting in a more compact globular conformation. The transition at the lower critical solution temperature（LCST） is often sharp, which allows for a wide range of smart material applications.At the LCST, oligo（ethylene glycol）-substituted polyisocyanides（PICs） form soft hydrogels, composed of polymer bundles similar to biological gels, such as actin, fibrin and intermediate filaments. Here, we show that the LCST of PICs strongly depends linearly on the length of the ethylene glycol（EG） tails; every EG group increases the LCSTand thus the gelation temperature by nearly 30 ℃. Using a copolymerisation approach, we demonstrate that we can precisely tailor the gelation temperature between 10 ℃ and 60 ℃and, consequently, tune the mechanical properties of the PIC gels.

Flow, thermal criticality and transition of a reactive third-grade fluid in a pipe with Reynolds' model viscosity

Neglecting the consumption of the material, a steady incompressible flow of an exothermic reacting third-grade fluid with viscous heating in a circular cylindrical pipe is numerically studied for both cases of constant viscosity and Reynolds＇ viscosity model. The coupled ordinary differential equations governing the flow in cylindrical coordinates, are transformed into dimensionless forms using appropriate transformations, and then solved numerically. Solutions using Maple are presented in tabular form and given in terms of dimensionless central fluid velocity and temperature, skin friction and heat transfer rate for three parametric values in the Reynolds＇ case. The numerical results for the velocity and temperature fields are also presented through graphs. Bifurcations are discussed using shooting method. Comparisons are also made between the present results and those of previous work, and thus verify the validity of the provided numerical solutions. Important properties of thermal criticality are provided for variable viscosity parameter and reaction order. Further numerical results are presented in the form of tables and graphs for transition of physical parameters, while varying certain flow and fluid material parameters. Also, the flow behaviour of the reactive fluid of third-grade is compared with those of the Newtonian reactive fluid.

Micromechanical properties of poly(N-isopropylacrylamide)hydrogel microspheres determined using a simple method

Temperature-responsive poly（N-isopropylacrylamide） （PNIPAM） hydrogel microspheres have attracted extensive attention because of their promising diverse biomedical applications. A quantitative understanding of the micromechanical properties of these microspheres is essential for their practical application. Here, we report a simple method for the characterization of the elastic properties of PNIPAM hydrogel microspheres. The results show that PNIPAM hydrogel microspheres exhibit elastic deformation and the obtained force-deformation experimental data fits the Hertz theory well. The moduli of elasticity of the PNIPAM hydrogel microspheres prepared under different conditions were systematically investigated in this work for the first time. The PN1PAM hydrogel microsphere composition significantly affects their micromechanical properties and their temperature sensitivity behavior. PNIPAM hydrogel microspheres with a larger equilibrium volume change have a lower modulus of elasticity. The modulus of elasticity of the PNIPAM hydrogel microspheres at body temperature （37 ℃, above the lower critical solution temperature （LCST） of PNIPAM） is much higher than that at room temperature （25 ℃, below the LCST of PNIPAM） because ofthermo-induced volume shrinkage and an increase in stiffness. These results provide valuable guidance for the design of smart materials for practical biomedical applications. Moreover, the simple microcompression method presented here also provides a versatile way to investigate the micromechanical properties of microscopic biomedical materials.

Supramolecular control over LCST behavior of hybrid macrocyclic system based on pillar[5]arene and crown ether

A hybrid system containing a pillar[5]arene unit and ten crown ether moieties was developed.The LCST behavior and thermo-responsive ness were successfully introduced into this pillar[5]arene-crown ether system.Both host-guest interactions and salting-out effect displayed great effects in realizing the supramolecular control over LCST properties and the rmo-re sponsiveness.Compa red with the individual macrocycles,this hybrid macrocycle system dramatically amplified the supramolecular control effect over LCST behavior.