DIFFERENTIAL SCANNING CALORIMETRY AND X-RAY DIFFRACTION STUDIES ON AGING BEHAVIOR OF Zn-Al ALLOYS

Decomposition processes of the quenched Zn-Al alloys were studied by differential scanning calorimetry (DSC), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results show that the stabilities of supersaturated solid solution (SSS) of Zn-Al alloy and α' phase formed by quenching would reduce with the increase of Zn content and the precipitation of η-Zn phases even when aging at ambient temperature, so that the exothermic precipitation peak in DSC curve would disappear. The activation energy of the η-Zn precipitation and the reaction enthalpy were calculated and measured. The kinetics of α' decomposition or η-Zn formation was determined by XRD. The microstructure change during aging was observed by TEM.

Studies of the Energy Release of Mitochondria from Sporophyte Cytoplasmic Male Sterile Rice by Differential Scanning Calorimetry

The differential scanning calorimetric (DSC)curves of the mitochondria isolated from two varieties of sporophyte cytoplasmic male sterile and their fertile lines of Yie Bai and Ma Xie type rice have been determined. The curves show that the energy is released continuously as temperature rise to 70℃. Some thermodynamic and kinetic parameters of the energy release of the mitochondria have been obtained. The presented results showed that the mitochondria from cytoplasmic male sterile rice released more heat and they had higher energy barrier, less rate, and more complicated mechanism than that of their fertile lines in the energy release process.

Application of differential scanning calorimetry to study the interpretation on herbal medicinal drugs:a review

Background:Differential scanning calorimetry as a method of investigating and monitoring the kinetics of herbal medicinal plants.Some instrumental and experimental aspects are discussed.Methods:A brief survey is made of herbal medicinal plants and results of differential scanning calorimetry studies are reviewed and this discussion is presented the effects of the instrumental conditions like heating rate and the sample conditions like sample particle size,sample mass,sample purity,sample stability in the melting region and property of impurities.Conclusion:This study suggests that application of differential scanning calorimetry to study the interpretation on herbal medicinal drugs.

Review of MEMS differential scanning calorimetry for biomolecular study

Differential scanning calorimetry （DSC） is one of the few techniques that allow direct determination of enthalpy values for binding reactions and conformational transitions in biomolecules. It provides the thermody- namics information of the biomolecules which consists of Gibbs free energy, enthalpy and entropy in a straightfor- ward manner that enables deep understanding of the structure function relationship in biomolecules such as the folding/unfolding of protein and DNA, and ligand bindings. This review provides an up to date overview of the applications of DSC in biomolecular study such as the bovine serum albumin denaturation study, the relationship between the melting point of lysozyme and the scanning rate. We also introduce the recent advances of the development of micro-electro-mechanic-system （MEMS） based DSCs.

ON A DIFFERENTIAL EQUATION FOR KINETICS OF NON- ISOTHERMAL CRYSTALLIZATION

A new differential equation was derived from the modified first-order kinetic model to describe the polymer crystallization processes. The crystallization experiments were carried out by means of DSC. Poly (ethylene terephthalate) resins were selected as the samples containing different catalysts. The relationships between the parameters obtained from the known Avrami equation and from one in the present paper were discussed. A method for applying the equation to determine the kinetic parameters from a constant heating and a constant cooling curve was proposed.

Influence of Rare Earth Elements on Microstructure and Mechanical Properties of Cast High-Speed Steel Rolls

The influence of rare earth （RE） elements on the solidification process and eutectic transformation and mechanical properties of the high-V type cast, high-speed steel roll was studied. Test materials with different RE additions were prepared on a horizontal centrifugal casting machine. The solidification process, eutectic structure transformation, carbide morphology, and the elements present, were all investigated by means of differential scanning calorimetry （DSC） and scanning electron microscopy energy dispersive spectrometry （SEM-EDS）. The energy produced by crack initiation and crack extension was analyzed using a digital impact test machine. It was found that rare earth elements increased the tensile strength of the steel by inducing crystallization of earlier eutectic γ-Fe during the solidification process, which in turn increased the solidification temperature and thinned the dendritic grains. Rare earth elements with large atomic radius changed the lattice parameters of the MC carbide by forming rare earth carbides. This had the effect of dispersing longpole M C carbides to provide carbide grains, thereby, reducing the formation of the gross carbide and making more V available, to increase the secondary hardening process and improve the hardness level. The presence of rare earth elements in the steel raised the impact toughness by changing the mechanism of MC carbide formation, thereby increasing the crack initiation energy.

Effects of Friction Heat on the Tribological Properties of the Woven Self-lubricating Liner

In the dry-sliding process of the woven self-lubricating liner which is used in the self-lubricating spherical plain bearing, the friction heat plays an important role in the tribological performances of the liner. It has important value to study on the relationship between tribological performances of the liner and the friction heat. Unforttmately, up to now, published work on this relationship is quite scarce. Therefore, the effect of friction heat on the tribological performances of the liner was investigated in the present work. The tribological behaviors of the liner were evaluated by using the high temperature end surface wear tester. Scanning electron microscopy （SEM） was utilized to examine the morphologies of worn surfaces of the liner and study the failure modes. Differential scanning calorimetry （DSC） measurement and X-ray diffraction （XRD） analysis were performed to study the behaviors of the wear debris. The temperature rise on the worn surface was calculated according to classical models. SEM observation shows that the dominating wear mechanism for the liner is mainly affected by friction shear force, contact pressure and friction heat. Higher fusion heat for the wear debris than that for the pure polytetrafluroethylene （PTFE） indicates that the PTFE is the main portion of the wear debris, and, the PTFE in the wear debris shows a higher crystallisation degree owing to the effects of friction shear force and the friction heat. Combining the calculated temperature rise results with the wear rate of the liner, it can be concluded that the effects of temperature rise o n the tribological performances of the liner become more obvious when the temperature rise exceeds the glass transition temperature （Tg） of the PTFE. The wear resistance of the liner deteriorates dramatically when the temperature rise approaches to the melting point （Ton） of the PTFE. The tribological performances of the liner can be improved when the temperature rise exceeds Tg but is far lower than Ton- The present study on the relationship between the temperature rise and the tribological performances of the liner may provide the basis for further understanding of the wear mechanisms of the liner as well as the relationship between the formation of the PTFE transfer film and the friction heat during the dry-sliding of the Finer.

Thermal decomposition and kinetics of plastic bonded explosives based on mixture of HMX and TATB with polymer matrices

This work describes thermal decomposition behaviour of plastic bonded explosives(PBXs) based on mixture of 1,3,5,7-tetranitro-1,3,5,7-tetrazocane(HMX) and 2,4,6-triamino-1,3,5-trinitrobenzene(TATB)with Viton A as polymer binder. Thermal decomposition of PBXs was undertaken by applying simultaneous thermal analysis(STA) and differential scanning calorimetry(DSC) to investigate influence of the HMX amount on thermal behavior and its kinetics. Thermogravimetric analysis(TGA) indicated that the thermal decomposition of PBXs based on mixture of HMX and TATB was occurred in a three-steps. The first step was mainly due to decomposition of HMX. The second step was ascribed due to decomposition of TATB, while the third step was occurred due to decomposition of the polymer matrices. The thermal decomposition % was increased with increasing HMX amount. The kinetics related to thermal decomposition were investigated under non-isothermal for a single heating rate measurement. The variation in the activation energy of PBXs based on mixture of HMX and TATB was observed with varying the HMX amount. The kinetics from the results of TGA data at various heating rates under non-isothermal conditions were also calculated by Flynn—Wall—Ozawa(FWO) and Kissinger-Akahira-Sunose(KAS)methods. The activation energies calculated by employing FWO method were very close to those obtained by KAS method. The mean activation energy calculated by FWO and KAS methods was also a good agreement with the activation energy obtained from single heating rate measurement in the first step decomposition.

Eutectic nucleation in Al-25wt.% Si alloy through DSC

Eutectic nucleation in hypereutectic Al-25wt.%Si alloy with the addition of P was studied by calculating the activation energy and nucleation work. The results indicate that P refinement, which can decrease the activation energy as well as nucleation work of eutectic solidification, can increase the eutectic nucleation frequency of Al-25wt.%Si alloy, so the addition of P can refme the eutectic structures of hypereutectic Al-Si alloys. According to the calculations, there is a certain relationship between the precipitation of primary silicon and eutectic solidification, and the eutectic nucleation mode is independent of morphology transition.

Crystallization Kinetics and Melting Behavior of PA1010/Ether-based TPU Blends

Polyamide 1010 （PA1010）/thermoplastie poly （ether urethane） elastomer （ether-based TPU） blends were prepared via melt extrusion. The crystallization kinetics and melting behavior of PA1010/ether-based TPU blends were systematically investigated using differential scanning calorimetry. The crystallization kinetics results show that the addition of ether-based TPU hinders the crystallization of PA1010, and the hindrance effect increases with the increase of the concentration of ether-based TPU. Both pure PA1010 and PA1010/ether-based TPU blends exhibit double melting peaks in the process of nonisothermal crystallization. The double melting peaks change differently with the variation of cooling rate and blend composition. The cooling rate only influences the lower melting peak; however, the blend composition influences not only the lower melting peak but also the higher melting peak. The reason for the phenomenon must be the interaction between the two compositions.

Aging behavior of a copper-bearing high-strength low-carbon steel

The effects of aging temperature and time on the hardness and impact toughness of a copper-bearing high-strength low-carbon steel were investigated. The hardness of the aged samples reached maxima after 1 h and 5 h of aging at 500 and 450℃, respectively; this increase in hardness was followed by a decrease in hardness until a temperature of 700℃, at which secondary hardening was observed. The impact toughness of the aged steel was found to be higher for 5 h of aging. Transmission electron microscopy confirmed the presence of carbide and copper precipitates; also, the secondary hardening could be the result of the transformation of austenite（formed in the aging treatment） to martensite. Differential scanning calorimetry of the steel was performed to better understand the precipitation behavior. The results revealed that the precipitation of the steel exhibited two significant stages of copper precipitate nucleation and coarsening of the precipitates, with corresponding activation energies of 49 and 238 kJ·mol^-1, respectively.

The Influence of Additives on Crystallization of Polyvinyl Chloride

Acetanilide, adipic acid and potassium hydrogen phthalate were chosen as nucleating agents of polyvinyl chloride（PVC）, and their effects on PVC crystallization were studied by differential scanning calorimetry, wide angle X-ray diffraction and fourier transform infrared spectroscopy. The experimental results indicate that all of the three additives are compatible with PVC to some extent, but adipic acid＇s compatibility with PVC is less satisfactory. The three additives can improve PVC crystallinity, and acetanilide can decrease PVC glass transition temperature（T）and narrow PVC melting range, while adipic acid and potassium hydrogen phthalate rise T of PVC and widen its melting range. All additives do not affect PVC crystal system and all g samples are in orthorhombic system. All additives can improve （200）, （110）, （210） and （201, 111） planes growing. Moreover, acetanilide and adipic acid can shrink PVC spacings and improve the crystal perfection of PVC, but potassium hydrogen phthalate swells spacings and reduces the perfection of PVC crystal.

Synthesis and Liquid Crystal Properties of Transition Metal Complexes of Meso-tetra(4-n-myristyloxyphenyl)porphyrin

Transition metal complexes of meso-tetra(4-myristyloxyphenyl)porphyrin TMPPM [M =Mn, Fe, Co, Ni, Cu, Zn; TMPP=mesotetra(4-myristyloxyphenyl)porphyrin] have been synthesized and characterized by means of elemental analyses, UV-Vis spectra, infrared photoacoustic spectra, 1H NMR spectra, molar conductance and differential scanning calorimetry(DSC). The ligand and the Zn complex show liquid crystalline behavior. According to the DSC thermogram of the Zn complex, it exhibits a lower phase transition temperature -7.453 ℃ and a wide mesophase temperature span, 77 ℃.

Effects of beryllium and iron additions on iron-bearing phase in A357 aluminum alloys

Iron is the most deleterious impurity in the Al-Si-Mg casting alloys and can easily form inter-metallic compounds that can significantly affect the subsequent behavior of material properties.Using differential scanning calorimetry (DSC) and microstructural analysis, how the Be and Fe additions affect the iron-bearing phase in A357 alloys was investigated.The results show that the iron-bearing phase in A357 alloy comprises mainly the plate-like β-Al5FeSi and a small quantity of the script-type π-Al8FeMg3Si6; and that the plate-like β-Al5FeSi proportion increases with increasing iron content in the alloy.The iron-bearing phase is mostly transformed from the plate-like β-Al5FeSi to the script-type π-Al8FeMg3Si6 with the addition of Be in the alloy.The hardness of alloy samples was also tested.The results show that both the increasing iron content and Be content can increase the hardness of the alloy.This may be contributed to the change of morphology and distribution of the iron-bearing phase in A357 alloy with the addition of iron or Be to the alloy.

Calorimetric Studies on Enthalpy Relaxation in Maltitol Glass Transition Based on Phenomenological Models

To investigate the enthalpy relaxation behavior of maltitol glass system,differential scanning calorimetry（DSC） was used to obtain the specific heat capacity[C p（T）] near the glass transition temperature（T g） at different cooling rates ranged between 1 and 20 K/min.Three phenomenological models of enthalpy relaxation,ToolNarayanaswamy-Moynihan（TNM） model,Adam-Gibbs-Vogel（AGV） model and Gómez Ribelles（GR） model,were used to simulate the experimental data.The models＇ parameters were obtained via a curve-fitting method.The results indicate that TNM and AGV models gave the almost identical prediction powers and can reproduce the curves of experimental C p（T） very well.However,the prediction power of GR model evolved from configurational entropy approach is not so good as those of TNM and AGV models.In particular,the metastable limit state parameter（δ） introduced by Gómez Ribelles has insignificant effect on the enthalpy relaxation of the small molecular hydrogen-bonding glass system.

Refinement and thermal analysis of hypereutectic Al-25%Si alloy

Refinement and thermal analysis of hypereutectic Al 25%Si alloy were investigated with scanning electron microscope (SEM) and differential scanning calorimeter (DSC). The results show that the average size of primary silicon in Al 25%Si alloy without and with phosphorus addition are 250 μm and 30 μm, respectively. But the primary and eutectic growth temperature is raised by about 17.3 ℃ and 4?℃ respectively due to phosphorus addition. The primary nucleation temperatures are 745.0 ℃ and 762.0 ℃ for untreated and treated samples and in addition, the enthalpy changes of primary and eutectic transformation are -261.0 J/g and -397.3 J/g without phosphorus addition, -294.2 J/g and -386.1 J/g with phosphorus addition, respectively. Otherwise the mechanisms of refinement and thermal transformation of Al 25%Si alloy in solidifying process are also discussed. [

Microstructure and properties of an Al–Ti–Cu–Si brazing alloy for SiC–metal joining

An Al–Ti–Cu–Si solid–liquid dual-phase alloy that exhibits good wettability and appropriate interfacial reaction with SiC at 500–600°C was designed for SiC–metal joining. The microstructure, phases, differential thermal curves, and high-temperature wetting behavior of the alloy were analyzed using scanning electron microscopy, X-ray diffraction analysis, differential scanning calorimetry, and the sessile drop method. The experimental results show that the 76.5Al–8.5Ti–5Cu–10Si alloy is mainly composed of Al–Al2Cu and Al–Si hypoeutectic low-melting-point microstructures (493–586°C) and the high-melting-point intermetallic compound AlTiSi (840°C). The contact angle, determined by high-temperature wetting experiments, is approximately 54°. Furthermore, the wetting interface is smooth and contains no obvious defects. Metallurgical bonding at the interface is attributable to the reaction between Al and Si in the alloy and ceramic, respectively. The formation of the brittle Al4C3phase at the interface is suppressed by the addition of 10wt% Si to the alloy. © 2017, University of Science and Technology Beijing and Springer-Verlag Berlin Heidelberg.

NUCLEATION AND CRYSTALLIZATION OF H-SHAPED(PS)_2PEG(PS)_2 BLOCK COPOLYMERS

A series of H-shaped （PS）2PEG（PS）2 block copolymers with different PS chain lengths were prepared. The influence of different confinements active on the crystallization and self-nucleation （SN） behavior of the PEG blocks was investigated by differential scanning calorimetry （DSC）. When the content of the crystalline block was high, a classical SN behavior was obtained. The block copolymer with PEG content of 49% （by weight） showed a classical SN behavior with a narrow self-nucleation domain and had bimodal crystallization exotherms. When the PEG dispersed as separated microdomains in the block copolymer, the self-nucleation domain disappeared and only annealing was observed.

CRYSTALLIZATION CHARACTERISTICS OF β-PHASE CRYSTALS IN COPOLYMERS OF POLYPROPYLENE WITH LOW ETHYLENE CONTENT

Polypropylene copolymers (CPP) containing β-nucleating agent were investigated by differential scanningcalorimetry (DSC), wide-angle X-ray diffraction (WAXD) and polarizing light microscopy (PLM). The results show thathigh content of β-phase crystals can also be formed for CPPs. Like PP homopolymers, the CPPs also have a most favorabletemperature near 132℃ for β-phase crystal growth. The crystallization rate of CPPs containing β-nucleating agent (β-CPP) ismuch greater than that of PP homopolymer containing β-nucleating agent (β-PP homopolymer). The observation ofspherulite morphology of β-CPP and β-PP homopolymer shows that the spherulites of β-CPP are more imperfect than thoseof β-PP homopolymer.

Homopolar bonds in Se-rich Ge-As-Se chalcogenide glasses

We have prepared three groups of Ge–As–Se glasses in which the Se content is 5.5 mol%, 10 mol%, and 20 mol%rich, respectively. We explored the possibility of suppressing the formation of the Ge–Ge and As–As homopolar bonds in the glasses. Thermal kinetics analysis indicated that the 5.5 mol% Se-rich Ge_（11.5）As_（24）Se_（64.5） glass exhibits the minimum fragility and thus is most stable against structural relaxation. Analysis of the Raman spectra of the glasses indicated that the Ge–Ge and As–As homopolar bonds could be almost completely suppressed in 20 mol% Se-rich Ge_（15）As_（14）Se_（71） glass.