Non-isothermal crystallization kinetics of reactive microgel/nylon 6 blends☆

The non-isothermal crystal ization kinetics of reactive microgel/nylon 6 blends was investigated by differential scanning calorimetry (DSC). The Mo equation was employed to analyze the non-isothermal crystallization data. The crystallization activation energies were also evaluated by the Kissinger method. The results show that the crystallization onset temperature (Tonset) and crystallization peak temperature (Tp) decrease with the increase of the content of reactive microgel, whileΔT (Tonset–Tp), the crystallization half-time (t1/2) and the crystal ization enthalpy (ΔHc) increase. The required cooling rates of blends are higher than that of neat nylon 6 in order to achieve the same relative crystallinity in a unit of time. The crystallization activation energies of the reactive microgel/nylon 6 blends are greater than those of the neat nylon 6. When the content of reactive microgel is 30%, the relative crystallinity (Xt) reaches the maximum.     

Isothermal and nonisothermal crystallization kinetics of bio-sourced nylon 69☆

Bio-sourced nylon 69,one of promising engineering plastics,has a great potential in developing sustainable technology and various commercial applications.Isothermal and nonisothermal crystallization kinetics of nylon 69 is a base to optimize the process conditions and establish the structure–property correlations for nylon 69,and it is also highly bene ficial for successful applications of nylon products in industry.Isothermal and nonisothermal crystallization kinetics has been investigated by differential scanning calorimetry for nylon 69,bio-sourced even–odd nylon.The isothermal crystallization kinetics has been analyzed by the Avrami equation,the calculated Avrami exponent at various crystallization temperatures falls into the range of 2.28 and 2.86.In addition,the Avrami equation modi fied by Jeziorny and the equation suggested by Mo have been adopted to study the nonisothermal crystallization.The activation energies for isothermal and nonisothermal crystallization have also been determined.The study demonstrates that the crystallization model of nylon 69 might be a twodimensional(circular)growth at both isothermal and nonisothermal crystallization conditions.Furthermore,the value of the crystallization rate parameter(K)decreases signi ficantly but the crystallization half-time(t1/2)increases with the increase of the isothermal crystallization temperature.To nonisothermal crystallization,the crystallization rate increases as the cooling rate increases according to the analysis of Jeziorny's theory.The results of Mo's theory suggest that a faster cooling rate is required to reach a higher relative degree of crystallinity in a unit of time,and crystallization rate decreases when the relative degree of crystallinity increases at nonisothermal crystallization conditions.     

Non-isothermal crystallization kinetics of polypropylene and hyperbranched polyester blends☆

Polypropylene (PP) with different contents of the second generation hyperbranched polyester (HBP) is prepared by melt blending method. The non-isothermal crystallization kinetics of PP and PP/HBP blend...     

增韧改性聚对苯二甲酸丁二酯/聚碳酸酯共混物非等温结晶动力学与力学性能

The polybutylene terephthalate (PBT）/ polycarbonate (PC）blends modified by toughening agent（S-2001）consisting of methyl methacrylate, styrene and silicone were prepared via melt blending.The non-isothermal crystallization kinetics of the blends were investigated by scanning calorimetry (DSC）at different cooling rate of 5℃·min^-1,10℃·min^-1,15℃·min^-1, and the data were analyzed by using modified Avrami theories of the Jeziorny method.The influence of toughening agent相似文献   

Non-isothermal crystallization kinetics and mechanical properties of olybutylene terephthalate/polycarbonate blends modified by toughening agent

The polybutylene terephthalate (PBT）/ polycarbonate (PC）blends modified by toughening agent（S-2001）consisting of methyl methacrylate, styrene and silicone were prepared via melt blending.The non-isothermal crystallization kinetics of the blends were investigated by scanning calorimetry (DSC）at different cooling rate of 5℃·min^-1,10℃·min^-1,15℃·min^-1, and the data were analyzed by using modified Avrami theories of the Jeziorny method.The influence of toughening agent相似文献   

间歇结晶器中维生素C的结晶热力学与动力学研究

The bench-scale cooling crystallization for ternary solution of L-ascorbic acid (Vitamin C) was studied.The solid-liquid phase diagram of Vitamin C-water-ethanol system was obtained on the basis of differential scanning calorimeter (DSC) curves. The heat of crystallization of Vitamin C was calculated with the aid of quantitative analysis. According to the population balance equation under unsteady state, the rates of nucleation and growth were determined. The parameters of crystallization kinetics equations were estimated by regression of experimental data. Crystal morphology and size were determined with x-ray diffraction and TA Ⅱ Coulter Counter.     

静态熔融结晶法提纯均四甲苯（英文）

The purification and separation of durene from the mixture containing durene isomers were studied. Since the boiling points of tetramethyl benzene isomers are very close but their melting points are of great differences, stat-ic melt crystallization was applied to separate and purify durene from its isomers. Crystallization experiments were carried out under various operating conditions. The effects of cooling rate, crystallization temperature, sweating temperature and sweating time on the yield and purity of crystal were investigated. Orthogonal exper-imental design method was adopted to analyze the factors that may affect the yield of durene. Under the optimal crystal ization conditions, the purity of durene could reach as high as 99.06%with the yield of 75.3%through one crystal ization process. By fitting purification data based on sweating time in isothermal operations, the purifica-tion rate coefficient was obtained.     

油酸修饰纳米CaCO3对PP结晶行为和力学性能的影响

Oleic acid (OA)-modified CaCO3 nanoparticles were prepared using surface modification method. Infrared spectroscopy (IR) was used to investigate the structure of the modified CaCO3 nanoparticles, and the result showed that OA attached to the surface of CaCO3 nanoparticles with the ionic bond. Effect of OA concentration on the dispersion stability of CaCO3 in heptane was also studied, and the result indicated that modified CaCO3 nanoparticles dispersed in heptane more stably than unmodified ones. The optimal proportion of OA to CaCO3 was established. The effect of modified CaCO3 nanoparticles on crystallization behavior of polypropylene (PP) was studied by means of DSC. It was found that CaCO3 significantly increased the crystallization temperature, crystal-lization degree and crystallization rate of PP, and the addition of modified CaCO3 nanoparticles can lead to the for-mation of β-crystal PP. Effect of the modified CaCO3 content on mechanical properties of PP/CaCO3 nanocompo-sites was also studied. The results showed that the modified CaCO3 can effectively improve the mechanical proper-ties of PP. In comparison with PP, the impact strength of PP/CaCO3 nanocomposites increased by about 65% and the flexural strength increased by about 20%.     

溶剂与杂质对11α-羟基-16α,17α-环氧黄体酮晶习的影响

The effects of solvent and impurity on the crystal habit of 11α-hydroxy-16α, 17α-epoxyprogesterone （HEP） grown from solution were studied by scanning electron microscope. Long prismatic crystals were produced when HEP was crystallized from pure acetone and N,N-dimethylformamide, while blocky crystals were produced from pure chloroform by cooling crystallization. One kind of isomorphic impurity, 16α, 17α-epoxyprogesterone （EP） was selected to examine its effect on the HEP crystal habit. When the content of EP in the mother liquor is very high （55.45%, solvent free basis）, the habit of produced HEP crystals was greatly modified from prismatic to octahedral. The differential scanning calorimetry and X-ray powder diffraction analyses showed that the change of crystal habit was originated from the crystal structure modification.     

一种新型成核剂对聚乳酸等温结晶行为的影响(英文)

The effect of a novel active nucleating agent(TBC8-eb) on the isothermal crystallization of poly(L-lactic acid) (PLLA) was studied by differential scanning calorimetry(DSC) and Fourier transform infrared spectroscopy(FTIR) . The analysis on kinetics demonstrates that TBC8-eb can not only accelerate the crystallization rate but also transform most of the original spherulite crystals of PLLA into sheaf-like crystals. Furthermore,the free energy of folding(σe) of PLLA and PLLA with TBC8-eb is 0.15 and 0.06 J·m-2,respectively,which suggests that the addition of TBC8-eb favors the regular folding of molecule chains in the crystallization of PLLA,improv-ing its crystallization rate. The FTIR results show that TBC8-eb can accelerate the conformational ordering of PLLA in the isothermal crystallization. The conformational ordering of PLLA nucleated with TBC8-eb begins with the interchain interaction of CH3,and then a short helix emerges where a couple of CH3 groups interact.     

间歇冷却结晶过程的模拟

The general mathematical model for batch cooling crystallization was established based on the population balance equation considering the change of slurry volume, and simulated with crystallization thermodynamics,kinetics and mass balance employing bed voidage. In the system of vitamin C-water-ethanol, reliability of this model was verified by comparison between simulation results and experimental data. The effects of operation parameters on product quality can be systematically investigated by modeling simulation.     

乙醇从葛根中提取黄酮动力学

The kinetics of leaching flavonoids from Pueraria Lobata with ethanol was investigated. The effects of leaching temperature, mechanical agitation rate, concentration of ethanol and feed particle size on leaching kinetics were examined. It is found that the smaller the feed particle size or the higher the leaching temperature, the higher the leaching rate. The leaching process can be described by the shrinking-core model. The apparent activation energy is 10.8kJ·mol^-1, suggesting that the leaching process is controlled by the inner diffusion. An empirical equation relating the flavonoids leaching rate constant to the feed particle size and leaching temperature was expected.     

Application of kinetics and computational fluid dynamics in pinene isomerization

A reliable kinetic model to describe the effects of various factors on the reaction rate and selectivity of pinene isomerization is developed. Furthermore, computational fluid dynamics(CFD) is applied to simulate the solid–liquid dispersion in reactor. The catalyst Ti M is obtained by improving the composition and structure of hydrated titanium dioxide. The kinetic equation of pinene isomerization is deduced based on reaction mechanism and catalyst deactivation model. The kinetic equation of pinene isomerization reaction is fitted, and the results show that the fitted equation is correlated with the experimental data. The rate and selectivity of pinene isomerization reaction are affected by the amount of catalyst, deactivation of catalyst, structure of catalyst, reaction temperature and water content of catalyst. The solid–liquid distribution of the reactor is calculated by computational fluid dynamics numerical simulation, and the solid–liquid dispersion in commercial scale reactor is more uniform than that in lab-scale reactor.     

Determination of metastable zone and induction time of analgin for cooling crystallization

The solubility, metastable zone width, and induction time of analgin for unseeded batch cooling crystallization in ethanol–aqueous system were experimentally determined. The solubility data could be well described by the van't Hoff equation model. The metastable zone width at various cooling rates was measured, and some parameters of nucleation kinetic were calculated using the Ny'vlt theory. Furthermore, the induction period of various temperatures and supersaturation ratios was also measured. According to classical nucleation theory, some nucleation parameters and interfacial energy was calculated through the induction time(t_(ind)) data. Homogeneous nucleation tended to occur when the supersaturation is high, whereas heterogeneous nucleation was more likely to occur when the supersaturation is low.     

EFFECT OF Ni CRYSTAL SIZE DISTRIBUTION ON THE ANTICOKING BEHAVIOR OF La-MODIFIED Ni/α-Al_2O_3 CATALYSTS

The crystal size distribution(CSD)was determined with small angle X-ray scattering technique.Theanticoking property of Ni-catalysts was investigated with the steam reforming of n-heptane in a TG-monitoredflow reactor.The results of this study show that the rate of coking on the supported Ni-catalysts depends main-ly on the percentage content of the large size fraction(25-70nm)of Ni-crystallites,and that the dispersion ofNi-crystallites and the anticoking property of the Ni/α-Al_2O_3 catalysts were promoted obviously by theLa_2O_3-modification method.The variation of the Ni-CSD and the anticoking property of the catalysts were fur-ther tested through different periods of hydrothermal treatment.It is found that the content of the largeNi-crystal size fraction and the coking rate pass correspondingly through a maximum.     

Freeze-drying and hot-pressing strategy to embed two-dimensional Ti0.87O2 monolayers in commercial polypropylene films with enhanced dielectric properties

The dielectric capacitor has been widely used in advanced electronic and electrical power systems due to its capability of ultrafast charging–discharging and ultrahigh power density.Nevertheless,its energy density is still limited by the low dielectric constant(≈2.2)of the commercial dielectric polypropylene(PP).The conventional enhancement strategy by embedding inorganic fillers in PP matrix is still difficult and challenging due to that PP hardly dissolves in any inorganic/organic solvent.In this work,we develop a new strategy including freeze-drying,surface functionalization,and hot-pressing to incorporate Ti_0.87O₂ monolayers in PP film.A series of uniform composited Ti_0.87O₂@PP film has been successfully fabricated with Ti0.87O2 content range of 0–15 wt%.The maximum dielectric constant of the as-prepared Ti_0.87O₂@PP film is 3.27 when the Ti_0.87O₂ content is 9 wt%,which is about 1.5 times higher than that of pure PP.Our study provides a feasible strategy to embed two-dimensional material into commercial PP thin-film with superior dielectric performance for practical application.     

Research on Steam Oxidation Resistance of Si_3N_4-bonded SiC Refractories

The steam oxidation of Si_3N_4-bonded SiC was determined at 1 000 ℃ for 50, 100, 150, 200, 250 and 300 h, respectively, according to ASTM C863-2000. The evolution of the phase composition and the microstructure as well as their relationship was investigated by XRD and SEM. The results show that the oxidation rate of Si_3N_4-bonded Si C is periodic. The presence of nitrogen element can impede the crystallization of SiO_2 glass; the local enrichment of CaO impurities is unfavorable for the existence of fibrous SiO_2. SiO_2 mainly exists as cristobalite when the CaO/SiO_2 ratio reaches a suitable level, but gradually transforms to quartz along with the oxidation time when the SiO_2 content increases, or the CaO/SiO_2 ratio decreases, due to the insufficient mineralization of CaO. The crystallization of SiO_2 glass, especially the formation of quartz is the key factor leading to the volume expansion and structural stress. When the cracks extend and reach the surface, the degradation of the material accelerates.     

Leaching Kinetics of Calcium Vanadate by Na2CO3 Solution

Leaching kinetics of calcium vanadate by Na2CO3 solution was studied. Kinetic equation was established according to the variation of VO3-concentration with time during the leaching process. The influences of initial pH value and stirring speed on reaction rate constant were examined and the corresponding apparent activation energy was calculated. The results indicate that the leaching process is a 0.68 order reaction, and the reaction rate constant 8.64×10-6 mol/(L-s). It increases with the increase of pH value and stirring speed. And the dissolution rate of calcium vanadate also increases. The apparent activation energy is 38.98 kJ/mol, and temperature has great influence on the leaching rate of calcium vanadate.     

Influence of Nano-Nd2O3 on Crystallization Mechanism of Fused Quartz

The isothermal crystallization kinetics of pure fused quartz of blank specimen N- 0 and specimen N- 3 in troduced with 3 mass% nano-Nd2O3 was researched by means of XRD and Avrami equation. The results show that crystallization mechanisms of fused quartz in two specimens are both heterogeneous nucleation type caused by surface structure defects,and the grain growth mode of two specimens are both two-dimensional growth ac companied by one-dimensional and three-dimensiona growths,specimen N- 3 has the higher degree of grain growth in one-dimensional and three-dimensional than specimen N- 0; introducing nano-Nd2O3 can obviously reduce the "active nucleation sites"of glass structure on the fused quartz particles surface,enhance the stability o glass structure,increase the activation energy of fused quartz crystallization from 874 k J · mol- 1to 1 270 k J·mol- 1,and decrease the crystallization rate of fused quartz obviously.     

一水盐酸环丙沙星初级成核机理的研究

A general expression for the ralationship between induction period and supersaturation was developed based on polynuclear approach.Different mechanism of primary nucleation in solution can be illustrated by the expression.The results of induction period determined by laser scatering method shows that the crystallization of ciprofloxacin hydrochloride monohydrate in water/ethanol or aqueous solution is by the mechanism of primary nucleation followed by one-dimensional diffusion growth,and then one-dimensional continuous or “birth and spread” growth on crystal face. The growth mechanism on the crystal face is affected by temperature and solvent.