Effects of rare earth oxides on viscosity,thermal expansion,and structure of alkali-free boro-aluminosilicate glass

Effects of rare earth oxides(Y_2O_3,La_2O_3,and Er_2O_3) on the viscosity,thermal expansion,and structure of alkali-free boro-aluminosilicate glasses were investigated by the rotating crucible viscometer,dilatometry and FT-IR absorption spectra.The results showed that the melting temperature of alkali-free boroaluminosilicate glasses decreased from 1 697.55 to 1 662.59,1 674.37 and 1 640.87 ℃ with the introduction of 1 mol%La_2O_3,Y_2O_3 and Er_2O_3,respectively.However,the glass transition temperature T_g,dilatometric softening temperature T_d and coefficient of thermal expansion of alkali-free boro-aluminosilicate glasses increased when adding the rare-earth oxides.At high temperatures,incorporating rare earth oxides into glass resulted in the peak at about 1 085 cm~(-1) towards lower wavenumber and the absorption band in the region of850-1 260 cm~(-1) broader,which indicated that rare earths acted as network modifiers and increased the numbers of non-bridging oxygen in the glass melts.However,the rare earths had an opposite effect and accumulated the glass structure at low temperatures near T_g.     

Crystallization kinetics of calcium aluminate glasses studied by non-isothermal techniques

The crystallization kinetics of 38.0CaO-38.0Al₂O₃-10.5BaO-6.5MgO-6.0Y₂O₃-1.0(Na₂O+K₂O) (wt%) glass was studied by differential scanning calorimeter (DSC) and X-ray diffraction (XRD) techniques. The results showed that DSC curves of calcium aluminate glass have a single glass transition temperature followed by one crystallization peak for the heating rates β = 5 K/min and two crystallization temperatures T _p1 and T _p2 for β ≥ 10 K/min. The activation energies of crystallization obtained from the Gao-Wang model of the first exothermal peak and the second exothermal peak of calcium aluminate glass are 340 and 662 kJ/mol, respectively. The Avrami exponents of the both crystallization peaks are approximately 2, indicating the twodimensional crystalline growth during its transformation from amorphous to crystalline. Ca₁₂Al₁₄O₃₃, Ca₃Al₂O₆ and unknown crystalline phases firstly appear when calcium aluminate glass is heat-treated. With the extending of heat-treatment duration, BaAl₂O₄ phase comes out.     

Synthesis and Characterization of Novel Polyarylene Sulfide

A novel polyarylene sulfide, polyarylene sulfide sulfone imide, was polymerized with a new monomer （Dichlorodiimide） and sodium sulfide by taking high temperature （200℃） N-methyl-2-pyrrolidinone （NMP） as solvent. The polymer was characterized by using conventional methods. Physical properties of the polymer, including thermal stability and solubility, were also studied. DSC and TG analyses reveal that the glass transition temperature T is equal to 252.4 ℃ and that the thermal decomposition temperature Td is equal to 484.9℃.     

Relationship between Liquid Phase Content and the Orientation of PMNT Ceramics by TGG Method

The effects of glass frit on the sintering and electric properties of PMN-PT textured ceramics were investigated. The glass frits, including PbO, Bi2O3 and ZnO, were selected since liquid phase sintering lowered the PMN-PT sintering temperature. The piezoelectric properties of PMN-PT ceramics with glass frit addition are strongly dependent on the densification. The addition of glass frits into PMN-PT matrix reduced the sintering temperature to 1 100 ℃ instead of 1 150 ℃ for samples without glass. The piezoelectric coefficients (d33) of PMN-PT textured ceramics achieved 568 pc/N with 1 wt% excess PbO.     

Melt synthesis and characterization of poly(L-lactic acid) chain linked by multifunctional epoxy compound

High molecular weight(Mw) poly(L-lactic acid)s(PLLAs) were synthesized using multifunctional epoxy compound(Joncryl-ADR4370) as chain extender. The products were characterized by gel permeation chromatography(GPC) and spectroscopy(¹HNMR and FTIR). The results indicated that the Mw of PLLA increased with the increasing of the ratio of epoxy compound and the extending of reaction time. The highest M _w of PLLA reached 360 000 g/mol when the ratio of epoxy compound was 1.5 wt%. However, the reactants turned to cross-linking when the ratio of epoxy compound was over 1.5 wt%. Differential scanning calorimetry(DSC) measurements demonstrated that the glass transition(T _g) and melting temperatures(T _m ) of products increased slightly as the increase of the molecular weight. Analysis of the hydrolytic degradation in vitro showed that the branched PLLA possessed the quicker degradability than that of the linear PLLA.     

Investigation on phase evolution of the ZnO-B<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiO<Subscript>2</Subscript> glass ceramics

ZnO-B₂O₃-SiO₂-Al₂O₃-Na₂O glass doped with nucleating agent TiO₂ was prepared with melting-quenching method and the effect of nucleating agent on the crystallization behavior and phase evolution of this glass was investigated by differential thermal analysis (DTA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The experimental results show that the glass transition temperature and the first crystallization temperature decrease from 630 °C and 765 °C to 595 °C and 740 °C, respectively, with introduction of TiO₂ into glass. There is no diffraction peaks in the XRD pattern but it is no longer transparent for the base glass without nucleating agent after heat treatment, which suggests the serious phase separation occurred, and the observation by SEM indicates that the phase separation is developed by nucleation and growth mechanism. However, there are two different crystals ZnAl₂O₄ and NaAlSiO₄ present in the glass containing TiO₂ after heat treating at 575 °C for 2 h and 740 °C for 6 h, respectively. What is interesting is that NaAlSiO₄ disappears as the crystallization time at 740 °C increases from 6 h to 12 h, and more ZnAl₂O₄ crystal is formed, namely, the further formation of ZnAl₂O₄ is at cost of NaAlSiO₄ with increasing crystallization time. And observation of the morphology of glass ceramics shows great difference with increasing crystallization time. Moreover, the ability of ZnO-B₂O₃-SiO₂-Al₂O₃-Na₂O glass ceramics against attacking of 1M HCl solution is increased by the crystals precipitated in heat treatment process.     

Preparation of layered potassium titanate whiskers with large length-diameter ratio by KDC method

Pure K2Ti4O9 whiskers were prepared by KDC(Kneading-Drying-Calcination) method with TiO2 and K2CO3 as raw materials. The influences of TiO2/K2CO3 molar ratio(RT/K), calcination temperature(TC) and cooling process on phase composition and morphology of the whiskers were investigated by TG-DSC(thermo gravimetric-differential scanning calorimeter), XRD(X-ray diffraction), and SEM(scanning electron microscope). Pure K2Ti4O9 potassium titanate whiskers with large length-diameter ratio(r)(over 250) can be obtained at RT/K = 2.9 and TC = 950 ℃.     

Study on Graphene Oxide Modified Inorganic Phase Change Materials and Their Packaging Behavior

We prepared the nano-inorganic phase-change "alloy" materials through the modification of Na_2SO_4·10H_2O using Na_2HPO_4·12H_2O and GO nano-nucleating agent, and further investigated their thermophysical properties such as melting/solidification temperatures and enthalpies via differential scanning calorimetry. When the weight ratio of Na_2SO_4·10H_2O and Na_2HPO_4·12H_2O was 8:2 and the weight ratio of graphene oxide was 0.5% of phase change material, the phase change "alloy" material showed excellent performances, specifically, the melting temperature and latent heat were found to be 22 ℃ and 190 J/g with a degree of subcooling decreased from 8.6℃ to 2.1℃. In order to extend the application of the phase change "alloy" material to building energy saving field, it was adsorbed on expanded glass beads under vacuum and further covered with diatomite. When the adsorption rate of EGB(volume) and PCAM(weight) was 2.5:1, the particle size of diatomaceous earth was found to be 3.6μm, while the best packaging result was obtained with the melting temperature and latent heat being 21℃ and 135 J/g, and no leakage was observed.     

Characterization of Ionic Conducting Cross-linked Polyether Electrolytes

An appropriate amount of toluene 2,4-diisocyanate（TDI） was added into polyether（[（CH2CH2O）13 CH2O]n/Li salt electrolyte to form a cross-linked network,with improving the film proces sability and thermal stability.The relation between the structure and ioinc conductive properties of the cross-lined polyether electrolytes was investigated by means of Fourier transform infra-red spectroscopy（FTIR）,differential scanning calorimetry（DSC）,mechanical property and AC impedance spectroscopy.The electrolytes system is found to have two glass transitions,and it is found that the two Tgs increase with increasing salt concentration.At the some Li salt concentration,the conductivity of cross-liked polyether/LiN（CF3SO2）2 complex system is higher than that of LiClo4,At EO/Li=25：1（mol ratio）,the former conductivity changes with temperature,while the later coincids with Arrhenius formula（σ=Ae^-Ea/RT）.The cross-linked polyether/LiN（CF3 SO2）2 electrolyte exhibits the maximum σ=10^-4.75S/cm at 30℃.     

Formation and mechanical properties of ductile Fe-based amorphous alloys using a cast iron with minor addition of B and Al

Fe-based amorphous alloys with ductility were synthesized using the commercial cast iron QT50 (denoted as QT) with the combining minor addition of B and Al by single roller melt-spinning. The melt-spun (QT_1-xB_x)₉₉Al₁ (x is from 0.006wt% to 0.01wt%) amorphous alloys exhibit onset crystallization temperatures and Curie temperatures of 759–780 and 629–642 K respectively, and which increase with B content. The amorphous ribbons are ductile and can be bent 180° without breaking. With the increase in B content from 0.006wt% to 0.01wt%, the Vickers microhardness of the amorphous alloys increases from Hv 830 to Hv 1110. The effects of the additional B and Al elements on the glass forming ability and mechanical properties were also discussed.     

Formation and thermal stability of Cu-Zr-Al-Er bulk metallic glasses with high glass-forming ability

The formation and thermal stabilities of Cu_46.25Zr_46.25-xAl_7.5Er_x, (x=0 to 8) bulk metallic glasses (BMGs) were investigated. The addition of a small amount of Er (2at%) for replacing Zr effectively improves the glass-forming ability of Cu_46.25Zr_46.25Al_7.5 alloy, and the glassy rod with a diameter of at least 12 mm can be formed. The glass transition temperature (T_g), temperature interval of supercooled liquid region ΔT_x (= T_x − T_g, and reduced glass transition temperature T_rg (=T_g/T₁) of Cu_46.25Zr_44.25Al_7.5Er₂ glassy alloy are 699 K, 62 K and 0.607, respectively.     

Glass formation of ternary Sin-based Sm-AI-Co bulk metallic glasses

Ternary Sm-based Sm-AI-Co alloys at specific compositions designed using an e/a- and cluster-related criteria exhibit high glass forming abilities and form bulk glassy rods of 3 mm in diameter by a copper mold suction-casting method. Four compositions of bulk metallic glasses (BMGs) are Sm₅₀Al₂₅Co₂₅, Sm₅₂Al₂₄Co₂₄, Sm₅₄Al₂₃Co₂₃ and Sm₅₆Al₂₂Co₂₂, which all satisfy a constant conduction electron concentration of 1.5. Among them, the BMG exhibiting the largest reduced glass transition temperature (T_rg) is Sm₅₀Al₂₅Co₂₅, which reaches 0.648. The glass transition temperature T_g and the onset crystallization temperature T_x of this alloy are respectively 579 and 640 K at a heating rate of 20 K/min.     

Microstructure and microwave dielectric properties of lead borosilicate glass ceramics with Al2O3

The effects of Al₂O₃ addition on both the sintering behavior and microwave dielectric properties of PbO-B₂O₃-SiO₂ glass ceramics were investigated by Fourier transform infrared spectroscope (FTIR), differential thermal analysis (DTA), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results show that with the increase of Al₂O₃ content the bands assigned to [SiO₄] nearly disappear. Aluminum replaces silicon in the glass network, which is helpful for the formation of boron-oxygen rings. The increase of the transition temperature T _g and softening temperature T _f of PbO-B₂O₃-SiO₂ glass ceramics leads to the increase of liquid phase precipitation temperature and promotes the structure stability in the glasses, and consequently contributes to the decreasing trend of crystallization. Densification and dielectric constants increase with the increase of Al₂O₃ content, but the dielectric loss is worsened. By contrast, the 3% (mass fraction) Al₂O₃-doped glass ceramics sintered at 725 °C have better properties of density ρ=2.72 g/cm³, dielectric constant ɛ _r =6.78, dielectric loss tan δ=2.6×10⁻³ (measured at 9.8 GHz), which suggest that the glass ceramics can be applied in multilayer microwave devices requiring low sintering temperatures.     

Morphology study of oriented SmBCO film deposited by MOCVD

c-axis-oriented SmBa_2Cu_3O_7(SmBCO) films have been deposited on(100)- LaA1O_3(LAO)substrate by metal organic chemical vapor deposition(MOCVD) technique.The effects of deposition temperature(T_(dep)) and total pressure(P_(tot)) on the orientation and microstructure of SmBCO films were investigated.The orientation of SmBCO films transformed from α-axis to c-axis with increasing of T_(dep) from 900 to 1 100℃.At T_(dep)=1 050℃,SmBCO films had c-axis orientation and tetragon surface.At P_(tot)~(dep)=400-800 Pa and T_(dep)=1 050 ℃,totally c-axis-oriented SmBCO films were obtained.The R_(dep) of SmBCO films increased firstly and then decreased with increasing P_(tot).The surface of SmBCO films exhibited tetragon morphology at 1 050 ℃ and400 Pa.Maximum thickness of SmBCO film deposited was 1.2μm at P_(tot)= 600 Pa,and the corresponding R_(dep)was 7.2 μm·h~(-1).     

Preparation and microstructure of spinel zinc ferrite ZnFe<Subscript>2</Subscript>O<Subscript>4</Subscript> by Co-precipitation method

Spinel zinc ferrites ZnFe₂O₄, prepared by co-precipitation method using the zinc nitrate Zn(NO₃)₂·6H₂O and ferric nitrate Fe(NO₃)₃·2H₂O as the raw materials, were characterized by the thermo gravimetric analysis (TG) and differential scanning calorimeter (DSC), X-ray diffraction (XRD) and scanning electron microscope (SEM). The influence of synthesis conditions, such as Zn/Fe molar ratio, pH value, the sintering temperature and time, on the microstructures was detailedly investigated. The relationships between the microstructures and the synthesis conditions were discussed. The results show that the pure spinel zinc ferrites ZnFe₂O₄ are formed when the Zn/Fe molar ratio is 1.05:2 at pH=8.5 or Zn/Fe molar ratio is 1:2 at Ph=9-10, and the precursors are sintered at 1100 °C for 4 h. Especially no other phases are observed when the Zn/Fe molar ratio is 1:2 at pH=10 and the precursor is sintered above 700 for 4 °C h. The higher sintering temperature and longer sintering time contribute to grain growth.     

Phase structure and electrical properties of La<Subscript>2</Subscript>O<Subscript>3</Subscript>-doped BiInO<Subscript>3</Subscript>-PbTiO<Subscript>3</Subscript> ceramics with high curie temperature

The phase structure and electrical properties of pure and La2O3-doped Bi-InO3-PbTiO3 （BI-PT） ceramics were studied respectively. In （1 -x）BI-xPT （x=0.72-0.80） ceramics, the stability of tetragonal phase increased with increasing x, and pure perovskite structure was obtained for x=-0.80 ceramics. The phase transition temperature range was between 575 ℃ and 600 ℃ for x=0.72-0.80 ceramics, higher than that of PT （-490 ℃）. The c/a ratio almost linearly decreased with increasing La2O3 content in x-0.80 ceramics. It is believed that Pb^2＋ vacancies were formed by La^3＋ substituting Pb^2＋ in La2O3-doped BI-PT ceramics. Tc shifted to lower temperature by 30 ℃/mol% La2O3. The maximum dielectric constant 8557 around 559 ℃ was exhibited in 0.5mol%-doped BI-0.80PT ceramics. La2O3-doped ceramics could be poled resulting from decreasing of c/a ratio and improving of dielectric loss and resistivity. The maximum piezoelectric coefficient d33 was 12 pC/N for 2mol%-doped BI-0.80PT ceramics.     

Electrochemical performance of LiFePO4/（C＋Fe2P） composite cathode material synthesized by sol-gel method

A LiFePO4/(C+Fe2P) composite cathode material was prepared by a sol-gel method using Fe(NO3)3·9H2O,LiAc·H2O,NH4H2PO4 and citric acid as raw materials,and the physical properties and electrochemical performance of the composite cathode material were investigated by X-ray diffractometry(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM) and electrochemical tests.The Fe2P content,morphology and electrochemical performance of LiFePO4/(C+Fe2P) composite depend on the calcination tempera...     

Effect of temperature on polishing and flatting time of float-formed Li<Subscript>2</Subscript>O-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiO<Subscript>2</Subscript> glass

Li₂O-Al₂O₃-SiO₂ glass prepared from traditional melting and cooling process was investigated. The surface characteristic of LAS glass was studied by simulating tin bath with different temperature and time, and the effect of surface tension/viscosity ratio on flatting time was analyzed. The results demonstrated that LAS glass can polish effectively when polishing at 1 300 for 8 °C min, and the optimum flatting and polishing temperature was 1 250–1 300 °C.     

Effect of ZnO-B<Subscript>2</Subscript>O<Subscript>3</Subscript> glass addition on the microwave dielectric properties of BaO-Nd<Subscript>2</Subscript>O<Subscript>3</Subscript>-TiO<Subscript>2</Subscript>-Bi<Subscript>2</Subscript>O<Subscript>3</Subscript> system

The effect of ZnO-B₂O₃(ZB) glass addition on the sintering behavior, microstructures and microwave dielectric properties of BaO-Nd₂O₃-TiO₂-Bi₂O₃ (BNTB) system was investigated with the aid of X-ray diffraction, scanning electron microscopy and capacitance meter. It is found that the ZB glass addition, acting as a sintering aid, can effectively lower the sintering temperature of BNTB system to 850 °C. The dielectric constant of BNTB-ZB ceramics increases with the increase of soaking time and the value of dielectric loss decreased with increasing soak time. The optical dielectric properties at 1 GHz of ɛ=74, tan δ=4×10⁻⁴, and TCC=25 ppm/°c were obtained for the BNTB system doped with 25 wt% ZB glass sintered at 850 °C for 2 h, representing that the BNTB-ZB ceramics could be promising for multilayer low temperature co-fired ceramics applications.     

Synthesis and Performance of Transparent Casting Polyurethane Resin

A series of transparent casting polyurethane resins (TCPU) were synthesized from cycloaliphatic diisocyaruae ( 1PDI or H12 MDI) , polyol, chain extender, crosslinking agents, catalyst and special aids (T),which were characterized by FTIR. The thermal stabilities of the obtained TCPU were examined by DSC and TGA , the glass transition temperature ( Tg ) was in the range of 95- 110 ℃ , the initial decomposition temperature (5% weight loss) was 250-265 ℃, and 10% weight loss at the temperature was in the range of 260-286℃ in nitrogen atmosphere. The morphologies of the fractured surfaces of TCPU were revealed by a scanning electron microscope (SEM). The crystalline-amorphous characters of TCPU were studied by WAXD, the result shows that TCPU possesses amorphous glassy characters. The optical properties of TCPU were studied by a UV7500 visible light absorbance measurement. All the samples exhibited excellent optical properties and possessed light transmittarwe in the range of 91%-93% .