Influence ofβ-nucleating Compound Agents on the Mechanical Properties and Crystallization Behavior of Polypropylene Random Copolymer

A novel polypropylene random(PPR)composite materials with optimized properties was developed by addingβ-nucleating compound agents(rare earth complex WBG-2 and aryl amide derivative TMB-5)and ternary compound modifier(TPE/WBG-2/CaCO_(3)).The effects of differentβ-nucleating agents and ternary compound modifier on the mechanical properties and crystallization behavior of PPR were analyzed.The results show that,compared with pure PPR materials,both WBG-2 and TMB-5 could significantly improve the impact strength of PPR.The crystallization temperature of PPR increased with the addition ofβ-nucleating agent.The modified PPR prepared with ternary compound modifier showed the most excellent comprehensive properties.

Effect of yttrium on thermal stability and crystallization behavior of Nd_(60)Fe_(20)Al_(10)Ni_(10) amorphous alloys

The effect of yttrium on the thermal stability and crystallization behavior of Nd-Fe-Al-Ni amorphous alloys was investigated using X-ray diffraction （XRD）, differential scanning calorimeter （DSC）, and transmission electron microscopy （TEM）.The results indicated that the as-cast Nd60Fe20Al10Ni10-xYx（X=-0, 2） amorphous alloys were fabricated with some quenched-in crystals, which could be restrained by Y. With the effect of yttrium, both the crystallization temperature and exothermic peak shifted to higher temperatures, illustrating that the thermal stability could be improved. The addition of Y changed the crystallization process and final crystallization results. Moreover, the crystallites in the amorphous matrix became more homogeneous and smaller. Meanwhile, Y was useful for the passivation of oxygen in chemistry and restrained the negative effect of oxygen. The activation energies of the start of crystallization and peaking were 1.21 and 1.16 eV, respectively, according to the Kissinger equation.

Influence of Carbon Nanofiber Addition on Mechanical Properties and Crystallization Behavior of Polypropylene

Carbon nanofiber （CNF）-reinforced polypropylene （CNF/PP） composites with different CNF contents were prepared by melt mixing, and the mechanical properties and crystallization behavior of the CNF/PP composites obtained were investigated. It was found that the tensile modulus of the composites was increased with the addition of CNFs, but their elongation at break and fracture strain energy were decreased, while the tensile strength of the composites was firstly increased and then decreased due to the agglomeration of CNFs at higher loading. Nonisothermal crystallization analysis showed that the CNFs played a role as nucleating agent in PP matrix, which led to increment in the crystallization rate and the degree of crystallinity of PP. Moreover, X-ray diffraction studies showed that the CNFs incorporated in the PP matrix favored the growth of （040）-oriented PP crystals. With the increase in the CNF content, the nucleating and orientation roles of the CNFs were obviously enhanced.

Effect of Rare Earth on the Crystallization Behavior of Li_2O-Al_2O_3-SiO_2 Glass-ceramic

X-ray powder diffraction and Fourier transform infrared spectroscopy were applied for characterization of Li2O-Al2O3-SiO2 glass-ceramic powders doped with Eu2O3,Gd2O3 and Er2O3,respectively,in the conditions of different heat-treatment temperatures and with various amounts.The powders were derived from the polyacrylamide gel method.The results show that,the wet gels prepared by polyacrylamide perform a unique crystallization behavior in the process of drying,comparing with some customary preparation such as melt processing.The main crystal phase and crystallization sequence of Li2O-Al2O3-SiO2 micro-powders have no distinct with addition of Eu2O3,Gd2O3 or Er2O3,while the crystallization temperature of the β-spodumene decreased and the amount of the β-spodumene increased.

Crystallization behavior of Fe_(78)Si_(13)B_9 metallic glass under high magnetic field

The effects of high magnetic field on the crystallization behavior of the Fe78Si13B9 metallic glass ribbon were studied. The samples were isothermal annealed for 30 min under high magnetic field and no field,respectively. Microstructure transformation during crystallization was identified by X-ray diffraction and transmission electron microscopy. It was found that the crystallizations of Fe78Si13B9 metallic glass processed under different conditions were that the precipitation of dendrite α-Fe（Si） and spherulite （Fe,Si）3B phases forms amorphous matrix and then the metastable （Fe,Si）3B phase transforms into the stable Fe2B phase. The grain size of the crystals is smaller and more homogeneous for the isothermal annealed samples under high magnetic field in comparison with that under no field indicating that the crystallization behavior of Fe78Si13B9 metallic glass is suppressed by high magnetic field.

Crystallization Behavior and Thermal Properties of PP/MgAl LDH Nanocomposites Prepared in Non-polar Solution

Polypropylene（PP）/MgAl layered double hydroxide（MgAl LDH） nanocomposites were synthesized by refluxing PP and dodecyl sulfate-intercalated MgAI LDH[MgAI（DS）] in non-polar xylene. Their structure, thermal and crystallization properties were studied via X-ray diffraction（XRD）, transmission electron microscopy（TEM）, thermogravimetric analysis（TGA）, differential scanning calorimetry（DSC）, and polarized light microscopy（PLM）. The nanoscaled dispersion of MgAI（DS） nanolayeres in the PP matrix was verified by the disappearance of the d（003） XRD diffraction peak of MgAI（DS） and observation of TEM image. The DSC data show that the SDS/LDH inorganic components negatively affect the crystallization properties of PP and decrease the size of PP sphcrulites because the inorganic components act as additional nuclei. The PP/MgA1 LDH nanocomposites have a faster charring progress in a temperature range of 250--430 ℃ and a better thermal stability above 320℃ than pure PP.

STUDIES ON THE MECHANICAL PROPERTIES AND CRYSTALLIZATION BEHAVIOR OF POLYETHYLENE COMPOSITES

The effects of interfacial modifier on the mechanical, dynamic mechanical properties and crystallization behavior of the polyethylene composites were investigated in the present paper. It was found that the interfacial modifer significantly improved the mechanical properties, influenced the dynamic mechanical spectra and slightly changed the crystallization behavior. The results showed that the interfacial modifier changed the dispersion state of dispersed phase of the composites, resulting in different phase structure, which was the major reason leading to different mechanical and crystallization properties.

MISCIBILITY AND CRYSTALLIZATION BEHAVIOR OF BIODEGRADABLE BLEND OF POLY(β—HYDROXYBUTYRATE)AND POLY(D,L—LACTIDE)—CO—POLY(ETHYLENE GLYCOL)

Studies on the miscibility of PHB/PELA blends showed that PHB and PELA were miscible in amorphous state.The crystallization behavior of PHB in the blend was strongly de- pendent on the addition of PELA component.

The Crystallization Behavior and Stability of Chromite Synthesized in Chromium-Containing Wastewater at Room Temperature

The ferrite process can not only purify wastewater containing heavy metal ions but also recycle valuable metals from wastewater. Therefore, it is considered a promising technology to treat chromiumcontaining wastewater. However, the process has not been extensively applied in industry due to its high synthesis temperature. In this paper, the feasibility of chromite synthesis at room temperature was comprehensively studied. The effects of critical factors on the effluent quality and the crystallization behavior and stability of the synthetic products were investigated. Results showed that the removal ratio of chromium from wastewater was over 99.0%, and the chromium concentration in the supernatant reached the sewage discharge standard after undergoing the ferrite process at room temperature. Increases in the aeration rate, stirring rate, and reaction time were favorable for the formation of stable chromite. The particles obtained by the ferrite process at room temperature were characterized by a compact structure, and the maximum size of the particles reached 52 μm. Chromium gradually entered the spinel crystal structure during the synthesis process, and the molecular formula of the synthetic chromite might be Fe3-xCrxO4, in which x was approximately 0.30. The path of the microscopic reaction was proposed to illuminate the synthesis mechanism of chromite under room temperature conditions. The present study has laid the foundation for the industrial application of the ferrite process in the purification and utilization of chromium-containing wastewater.

Crystallization Behavior of Polymer Derived Silicon Carbide Sintered Through Microwave Heating Technique

A self-crosslinkable liquid highly branched polycarbosilane（LHBPCS） with 5.07% vinyl group and a C/Si ratio of 1.33 was used as the precursor to prepare Si C ceramic material. Microwave heating technique and conventional heating method were applied for the heating treatment process. It was found that, compared with conventional heating method, microwave heating technique could enhance the crystallinity of Si C ceramic material with small grain size at much lower curing temperature and within shorter time. In addition, the SiO_2 additive could lead to less α-Si C and excess carbon, but worsen the crystallinity of β-Si C in the final samples.

The Crystallization Behavior of L-Poly(lactic acid)/Polypropylene Blends:The Acceleration for Both L-Poly(lactic acid)and Polypropylene

For a polymer/polymer dismissible blend with two crystallizable components,the crystallization behavior of different components and the reciprocal influences between different crystals are interesting and important,but did not investigate in detail.In this study,the L-poly(lactic acid)/polypropylene(PLLA/PP)blends with different weight ratios were prepared by melt mixing and the crystallization behavior of the blends were investigated.Results showed that the crystalline structures of PLLA and PP were not altered by the composition.For the crystallization of PLLA,both the diffusion of chain segments and crystallization rate were enhanced under the existence of PP crystals.For the crystallization of PP,its crystallization rate was depressed under the existence of amorphous PLLA molecular chains.When the PP crystallized from the existence of PLLA crystals,although the diffusion rate of PP was reduced by PLLA crystals,the nucleation positions were obviously enhanced,which accelerated the formation of PP crystals.This investigation would supply more basic data for the application of PLLA/PP blend.

Study on crystallization and microstructure of Li_2O-Al_2O_3-SiO_2 glass ceramics

Lithium aluminosilicate （LAS） glasses are generally difficult to prepare because of their high melting temperature. In this study, the preparation of LAS glasses was achieved at a relatively low melting temperature. The batch containing MgO-ZnO-LiEO- Al2O3-SiO2 was melted in a platinum crucible at 1550℃ for 2 h and was then followed by two- or three-step heat treatment processes for nucleation and crystal growth. The characterizations were carried out by differential thermal analysis, X-ray diffraction, infrared spectroscopy, scanning electron microscopy, and UV-Vis-NIR scanning spectrophotometry. The hexagonal stuffed β-eucryptite solid solution crystallized at 840-960℃. Most of the hexagonal β-eucryptite solid solution transformed into the tetragonal β-spodumene solid solution at 1100℃. Almost all the aluminum atoms entered into the tetrahedral sites in the aluminosilicate network of the 6- eucryptite/β-quartz solid solution. All of the Al atoms did not belong to the aluminosilicate network of the β-spodumene solid solution. The glass ceramic with a mean grain size of 10-20 nm is transparent, the transmittance reaches -85% in the visible light wavelength.

Preparation,Structures,Thermal Properties and Sintering Behaviors of B_2O_3-SiO_2-ZnO-BaO-Al_2O_3 Glass

B_2O_3-SiO_2-ZnO-BaO-Al_2O_3 glass with different Al_2O_3 contents（1mol%, 3mol%, 5mol%, and 7mol%） was prepared, and it was intended to be used as lead-free and low-melting glass sealants for solid oxide fuel cells. The effects of Al_2O_3 content on the structures, thermal properties, and sintering behaviors of the B_2O_3-SiO_2-ZnO-BaO-Al_2O_3 glass were investigated in detail. The Al_2O_3 content largely influenced the structures and thermal properties of the glass. When the Al_2O_3 content 5mol%, the transition temperature of the glass decreased with the Al_2O_3 content, while the crystallization temperature increased with the Al_2O_3 content. However, higher Al_2O_3 content degraded the stability of the glass. The B_2O_3-SiO_2-ZnO-BaO-Al_2O_3 glass with 5 mol% Al_2O_3 content exhibits the optimal sintering densification characteristics and can be used as glass sealants for solid oxide fuel cells.

Study on the Phase Transformation Behavior of Nanosized Amorphous TiO2

Nanosized amorphous TiO2 powders with a specific surface area of 501 m2·g-1 were prepared by hydrolysis. After calcined at 400℃ for 2 h, the prepared amorphous TiO2 powders were fully transformed into anatase crystallites with a specific surface area of 141 m2·g-1. Differential scanning calorimetric (DSC) experiments were performed on the samples of nanosized amorphous TiO2 mixed with microsized anatase, nanosized anatase, or nanosized α-Al2O3 respectively. Effects of sample packing, anatase addition, or α-Al2O3 addition on the crystallization behavior of nanosized amorphous TiO2 were analyzed.

Crystallization and microstructure evolution of amorphous Al_(85)Y_4Nd_4Ni_7 alloy

The mixture model of Al_(85)Y_4Nd_4Ni_7 alloy in which a partiallycrystallized amorphous alloy is regarded as a nanocornposite of an Al nanoparticle and a remainingamorphous matrix is presented. Its evolution in the process of crystallization has been investigatedby differential scanning calorimetry (DSC), X-ray diffraction (XRD), and transmission electronmicroscopy (TEM). Mainly amorphous structure with alpha-Al nanocrystals embedded in the amorphousmatrix has been revealed by melt spining the alloy. Crystallization is showed to occur in threestages: (1) crystallization of amorphous alloy and formation of AINiY, AINdNi and unknowncrystalline phases, (2) formation of Al_3 Y and Al_3Nd, and (3) formation of Al_3Ni.

Crystallization Behevior of Poly(3-dodecylthiophene)

The crystallization behavior of poly (3-dodecylthiophene) (P3DDT) is studied bq differential scanning calorimetry (DSC) under different cooling rates. When the methods of Jeziorny., Ozawa and a new one proposed by our laboratory are applied to describe its nonisothermal crystallization behavior, the new one is confirmed to be the best and convenient. By determining kinetic parameters, the analysis of the nonisothermal crystallization behavior is performed. According to Kissinger method, the crystallization activation energy of P3DDT is also evaluated.

Synthesis,Crystal Structure and Magnetic Behavior of a Novel Cd(Ⅱ) Complex with Four Nitroxide Radicals

A novel diamagnetic-metal Cd（Ⅱ） complex with four nitroxide radicals[Cd（IM4Py）4Cl2]（IM4Py=2-（4＇-pyridinyl）-4,4,5,5-tetramethylimidazoline-1-oxyl） was synthesized and characterized by elemental analyses,IR spectra,UV-Vis spectra and X-ray single crystal diffraction.The complex crystallized in triclinic space group P1 with a=0.93285（14） nm,b=1.16827（18） nm,c=1.3660（2） nm,α=112.759（2）°,β=104.524（2）°,γ=92.008（3）°,V= 1.3143（3） nm3,Z=1,Dc=1.335 g/cm3,the final R1=0.0423 and wR2=0.1009.In the title complex,each Cd（Ⅱ） ion adopting a distorted octahedral geometry is coordinated by two Cl-anions and four pyridyl-N atoms from four IM4Py ligands.The magnetic measurements show the weak antiferromagnetic interactions between the nitroxide radicals.

Studies on the Phase Behavior of Lyotropic Liquid Crystal in DAD/C_4OH/n-C_8H_(18)/D_2O System

The lytropic liquid crystals in dodecanic acid diethanolamine (DAD) /n-butanol (C4OH) /octane (n-C8H18) /deuteron (D2O) system were studied to determine the phase regions and were investigated by 2H-NMR spectroscopy,optical polarizing microscope and small-angle X-ray diffraction (SAXD) methods.The results indicate that the lamellar,hexagonal and cubic liquid crystals all exist in the above system.Keeping the weight ratio of DAD and C4OH constant,the microphase Structure,2H quadruple splitting and the interlayer spacing are all changed with the addition of deuteron.

Effect of Gallium Addition on Magnetic Properties of Nd_2Fe_(14)B-Based/α-Fe Nanocomposite Magnets

The influence of Ga addition on the crystallization behavior and the magnetic properties of nanocomposite Nd2Fe14B-based/α-Fe magnets was investigated. It was found that the addition of 0.2% did not change the crystallization temperature of amorphous alloy, but the magnetic properties were improved significantly because of the strong exchange coupling interaction between the hard and soft magnetic phases. The optimum magnetic properties with iHc = 600. 3 kA· m^-1, B r = 0.75 T, and （BH）max = 88.03 kJ· m^-3 were obtained in bonded Nd9.5（FeCoZr）83.8 Ga0.3 B6.5 magnet with 15 m·s^- 1 wheel speed and 670 ℃ annealing treatment. The apparent improvement of magnetic properties originates from the grain refinement calculated using the Scherrer formula from corresponding XRD patterns and the excellent rectangularity of the demagnetization curve.

Formation and crystallization behavior of Fe-based amorphous precursors with pre-existingα-Fe nanoparticles-Structure and magnetic properties of high-Cu-content Fe-Si-B-Cu-Nb nanocrystalline alloys

Structure,crystallization behavior,and magnetic properties of as-quenched and annealed Fe_(81.3)Si_(4)O_(13)Cu_(1.7)(Cu1.7)alloy ribbons and effects of Nb alloying have been studied.Three-dimensional atom probe and transmission electron microscopy analyses reveal that high-number-density Cu-clusters and Pre-existing Nano-sized a-Fe Particles(PN-a-Fe)are coexistence in the melt-spun Cu1.7 amorphous matrix,and the PN-α-Fe form by manners of one-direction adjoining and enveloping the Cu-clusters.Two-step crystallization behavior associated with growth of the PN-a-Fe and subsequent nucleation and growth of newly-formedα-Fe is found in the primary crystallization stage of the Cu1.7 alloy.The number densities of the Cu-clusters and PN-a-Fe in melt-spun Fe8_(1.3-x)Si_(4)B_(13)Cu_(1.7)Nb_(x)alloys are gradually reduced with enriching of Nb,and a fully amorphous structure forms at 4 at.%Nb,although smaller Cu-clusters still exist.After annealing,2 at.%Nb coarsens the average size(D_(α-F)e)of theα-Fe grains from 14.0 nm of the Nb-free alloy to 21.6 nm,and 4 at.%Nb refines the D_(α-Fe)to 8.9 nm.The mechanisms of theα-Fe nucleation and growth during quenching and annealing for the alloys with large quantities of PN-α-Fe as well as after Nb alloying have been discussed,and an annealing-induced oc-Fe growth mechanism in term of the barrier co-contributed by competitive growth among the PN-a-Fe and diffusion-suppression effect of Nb atoms has been proposed.A coercivity(HC)αDα-Fe^(3)correlation has been found for the nanocrystalline alloys,and the permeability is inverse with the H_(C).