MORPHOLOGY AND STRUCTURE OF TRANSFORMATION PRODUCTS FORMED AT INTERMEDIATE TEMPERATURE IN A Cu-Zn-Al ALLOY

A TTT diagram for th ie precipitation formed at some intermediate temperatures through cooling from high lemperalure parenl phase in a Cu-27 27Zn-3.73Al allay is established by means of dilatormetric measurement.The morphology and structure of transformation products formed at some intermediate tem peratures isothermally through cooling from high temperature parent phase and up-quenching from DO_(3) parent phase are studied by metallographic.X-ray and electron microscopy analyses.Three regions in the two separate C curves are obtained according to different morphology of precipitate:rod-like a,plate-like bainite and a rods,and bainite plates.Prolonged aging makes bainite plate change gradually into a whose lattice parameters are no different from that of a formed equilibriumly from parent phase.The structure is almost orthorhombic long period structure for bainites formed from B_(2) and DO_(3) parent phase,but monoclinic for martensite from DO_(3).They correspond to the overlapping and separating of(1210)and(2010)diffraction peaks respectively,showing the lower degree of ordering in bainite.

Influence of Konjac Glucomannan on the Crystallization Morphology and Structure of Calcium Oxalate

The influence of additive Konjac Glucomannan （KGM） in a variety of con- centrations on the crystallization morphology and structure of calcium oxalate （CaOxa） has been investigated by infrared spectroscopy, scanning electron microscope, X-ray diffraction and so on. The results showed KGM can complex with the Ca^2＋ ions; low concentration KGM prevents CaOxa from aggregating, raises the concentration of ions in the solution, reduces the quantity of crystals and inhibits their growth, and the crystals are round and blunt; while high concentration KGM promotes the growth of crystal, which appears in sheet-like or irregular shape. Only CaOxa monohydrate was observed in a certain system with or without the presence of KGM.

Morphology and Structure of SiO_2 Film Using Thermal Oxidation Process on(111)Silicon Crystals in Dry Oxygen Atmosphere

By means of scanning electron microscope(SEM)and high voltage electron microscope(HVEM)we have observed and analysed morphology and micro-structure of silicon oxide film with different thickness formed on(111)silicon monocrystal under dry oxygen atmosphere at 1100℃.Compared with their oxidation kinetic curves consisted of three stages,we suggested a mechanism on forming silicon oxide film.According to electron and X-ray diffraction analyses the silicon oxide films consisted of silica with different crystal structure.We also have discussed a stacking fault and a dislocation formed in the Si-Sio_2 interface region simulaneously forming silicon oxide film.

THE MORPHOLOGY AND STRUCTURE OF ETHYLCYANOETHYL CELLULOSE IN STYRENE AND POLYSTYRENE

Ethyl-cyanoethyl cellulose ((E-CE)C)/styrene solution could form anisotropic system when the concentration was high enough. The (E-CE)C/polystyrene(PS)multiphase polymer could be obtained by radical polymerization of the styrene in the solution. The (E-CE)C/PS multiphase polymer maintained both the crystalline structure of the (E-CE)C and the amorphous structure of the PS. In the multiphase polymer produced from the isotropic solution, however, the (E-CE)C formed spherulites and spread in the PS amorphous phase. While, in the multiphase polymer produced from the anisotropic solution, the (E-CE)formed cylinderic crystalline aggregates. Moreover, the ordered lamellar texture was also observed in the multiphase polymer produced from the anisotropic solution.

INVESTIGATION OF STRUCTURE AND PROPERTIES FOR POLYMER SYSTEMS BASED ON DYNAMIC RHEOLOGICAL APPROACHES

The dynamic rheological measurements have been a preferred approach to the characterization of the structure and properties for multi-component or multi-phase polymer systems,due to its sensitive response to changes of structure for these heterogeneous polymers.In the present article,recent progresses in the studies on dynamic rheology for heterogeneous polymer systems including polymeric composites filled with inorganic particles,thermo-oxidized polyolefins,phase- separated polymeric blends and functional polymers with the scaling and percolation behavior are reviewed,mainly depending on the results by the authors' group.By means of rheological measurements,not only some new fingerprints responsible for the evolution of morphology and structure concerning these polymer systems are obtained,the corresponding results are also significant for the design and preparation of novel polymer-based composites and functional materials.

STUDIES ON STRUCTURE AND PHASE BEHAVIOR OF MULTICOMPONENT POLYMERS THROUGH RHEOLOGICAL TESTS

Rheological measurement has been a preferred approach to the characterization of the structure and phase behaviors for multi-component/multi-phase polymer systems, due to its sensitive response to the changes of structure for these heterogeneous polymers. In the present article, recent progresses in the studies on rheology for heterogeneous polymer systems including phase-separated polymeric blends and block copolymers are reviewed, mainly depending on the results by the authors＇ research group. By means of rheological measurements, not only some new fingerprints responsible for the evolution of morphology and structure concerning these polymer systems are obtained, also the corresponding results are significant for design and preparation of novel polymeric structural materials and functional materials.

Morphologies and Structures of Perovskite Thin Film on Zn-face and O-face of ZnO Single Crystal

ZnO single crystal was used as the substrate to study the effect of ZnO crystal plane polarity on the morphology and structure of CH_3NH_3PbI_3（MAPbI_3） perovskite film and carrier transport properties,which is meaningful for improving ZnO-based perovskite solar cell. It is found that perovskite thin film has small grain size（about 190 nm） and high coverage rate on the O-face of ZnO single crystal,and the dominant exposed crystal plane of perovskite film is（110） plane. While the MAPbI_3 thin film has large grain size（about 1.03 μm） and low coverage rate on the Zn-face,and the（022） plane is dominantly exposed for the perovskite film. The injection of photogenerated electrons from MAPbI_3 film into the O-face of ZnO single crystal is faster and more effective than that to Zn-face. It is supposed that O-face is more suitable for ZnO single crystal based perovskite cell fabrication than Zn-face.

Characteristics of Central Heating Cinder and Its Influence on Soil Properties

[Objective]The research was designed to explore the effect of long-term stacking of solid waste produced in the coal-burning process of central heating enterprises on physical and chemical properties of soil.[Method]This study took the heating enterprises in Shenyang City as the research object.The morphological structure and element composition of coal cinder were determined by continuously collecting coal and cinder samples in different periods.At the same time,the original soil and cinder soil of the stacking site were collected to determine the changes of soil morphological structure,element composition and physical and chemical properties,so as to provide reference for the resource utilization of local cinder waste and the potential pollution risk of the stacking site.[Result]The contents of C,H,O,N,and S non-metallic elements in coal cinder decreased by 69.5%,71.2%,76.0%,74.5%,and 34.6%,respectively when compared with raw coal;while the content of Si increased significantly by 95.7%.The contents of Al,K,and Fe in cinder decreased by 4.3%,60.2%,and 33.3%,respectively,while the contents of Mg and Na increased by 36.1%and 130.9%,respectively.Compared with the original soil,the contents of C,H,and O in shallow cinder soil and deep cinder soil increased by 126.5%,67.9%,80.93%,and 21.3%,25.0%and 42.3%,respectively.The residual carbon existed in the form of activated carbon.The contents of Mg,Al,K,Na,Ca,and Fe in shallow cinder soil and deep cinder soil increased by 61.6%,5.4%,46.1%,35.8%,32.5%,6.3%and 22.3%,12.3%,12.2%,15.6%,5.8%and 2.8%,respectively compared with the original soil.The content of heavy metal elements in coal cinder did not reach the detection limit.Under the scanning electron microscope,the raw coal is mainly block structure,while the cinder is honeycombed and porous and dust.[Conclusion]Cinder stacking can significantly improve the content of organic matter and available K in shallow cinder soil,and improve the porosity and permeability of soil.In addition,cinder waste has high pH and pore structure,which can be used as acid soil conditioner,seedling flower matrix and compound fertilizer filler to take full advantage of cinder waste,improve soil structure and supply nutrients.

EFFECT OF POLY(BUTYLENE SUCCINATE) ON THE MORPHOLOGY EVOLUTION OF POLY(VINYLIDENE FLUORIDE) IN THEIR BLENDS

The effect of PBS on the morphological features of PVDF has been investigated by optical and atomic force microscopies under various conditions. It was found that neat PVDF forms large γform spherulites with extraordinarily weak birefringence at 170℃. Adding 30% PBS makes PVDF exhibit intrigued flower-like spherulitic morphology. The growth mechanism was explained by the decrease of the supercooling and the materials dissipation. Increasing the PBS content to 70% favors the formation of ring banded spherulites. Temperature dependent experiments verify the α→γ phase transition occurs from the junction sites of the ot and y crystals, while starts from the centers of α spherulites in the blends. Ring banded structures could be observed in neat PVDF, 70/30 blend and 30/70 blend when crystallized at 155℃, without γ crystals. The band period of PVDF α spherulites increases with crystallization temperature as well as the amount of PBS content. At 140℃, spherulites in neat PVDF lose their ring banded feature, while coarse spherulites consisting of evident lamellar bundles could be found in 30/70 blend.

Corrosion Behavior of Ferritic/Martensitic Steels CNS-Ⅰ and Modified CNS-Ⅱ in Supercritical Water

The corrosion behaviors of CNS-I and modified CNS-II were evaluated by exposing to superciritical water （SCW） at 550℃ and 25 MPa with a dissolved oxygen concentration of 200× 10 ^-9 for up to 1 000 h. Detailed corrosion results of these two alloys were provided, including the growth rate of the oxide scales, microstructure of the oxide scales, distribution of phases and alloying elements. The mass gains of CNS-I and modified CNS-II were 609.73 mg/dm2 and 459.42 mg/dm2 , respectively, after exposing to SCW for 1 000 h. A duplex oxide scale with an outer porous magnetite layer and an inner relatively dense magnetite/spinel-mixed layer was identified on CNS-I and modified CNS-II after the test. The oxide scales were rather porous at the beginning of the test but the porosity decreased with increase of the exposure duration. It was found that Fe was enriched in the outer oxide layer, Cr was enriched in the inner oxide layer and O existed at a very high concnetration in the whole oxide scale. Other alloying elements such as Mo, W, Mn were depleted from the outer oxide layer and showed slightly enrichment in the inner oxide layer. The distributution of Ni was different from other elements, it was enriched in the interface bewteen the base metal and the oxide scale and depleted in the outer and inner oxide layers.