Crystallization,morphology, structure and thermal behaviour of nylon-6/rubber blends

An experimental study was carried out in order to investigate the morphological, kinetic, structural and thermodynamic properties of nylon-6/rubber (namely ethylene-propylene copolymer (EPM) and ethylene-propylene copolymer functionalized by inserting along its backbone succinic anhydride groups (EPM-g-SA)) blends. The morphology and the overall kinetics of crystallization of the blends strongly depend on the type of copolymer added to nylon and on the blend composition. The EPM-g-SA acts as a nucleating agent for the Ny spherulites and at the same time causes a drastic depression of the overall kinetic rate constant. This decrease is related to the increase of the melt viscosity observed in Ny/EPM-g-SA blends. The crystalline lamella thickness of the Ny phase in the blends is lower than that of pure Ny crystallized at the same T_c suggesting that the presence in the melt of an elastomeric phase disturbs the growth of the Ny crystals. The rubber does not influence the thermal behaviour of the nylon. The results found lead to the conclusion that in the melt nylon-6 is incompatible with both EPM and EPM-g-SA copolymers.     

含多羟基功能基树脂的合成及其与硼酸螯合性能的研究

合成了数种含有多羟基醇单醚功能基的树脂，研究了反应条件及树脂的吸附性能。     

DSC and TMDSC study of melting behaviour of poly(butylene succinate) and poly(ethylene succinate)

The subsequent melting behaviour of poly(butylene succinate) (PBSU) and poly(ethylene succinate) (PES) was investigated using DSC and temperature modulated DSC (TMDSC) after they finished nonisothermal crystallization from the melt. PBSU exhibited two melting endotherms in the DSC traces upon heating to the melt, which was ascribed to the melting and recrystallization mechanism. However, one melting endotherm with one shoulder and one crystallization exotherm just prior to the melting endotherm were found for PES. The crystallization exotherm was ascribed to the recrystallization of the melt of the crystallites with low thermal stability, and the shoulder was considered to be the melting endotherm of the crystallites with high thermal stability. The final melting endotherm was ascribed to the melting of the crystallites formed through the reorganization of the crystallites with high thermal stability during the DSC heating process. TMDSC experiments gave the direct evidences to support the proposed models to explain the melting behaviour of PBSU and PES crystallized nonisothermally from the melt.     

用CCD摄像法测量下喷环流反应器内的气泡行为

本文开发了一种集高速视频分析系统和计算机数字图像处理技术于一体的具有普适性的动态高速ＣＣＤ摄像系统，并利用该系统测定了两相三维下喷环流反应气内的环境气泡行为，考察了不同喷咀和操作条件对气泡行为及平均传质比表面积的影响。     

Effect of Resins on Asphaltene Self‐Association and Solubility

In previous studies, asphaltenes and resins have been treated as two distinct fractions of a crude oil. The asphaltenes were assumed to be the only self‐associating fraction. However, there is evidence that resins also participate in this self‐association. In this study, molar masses of mixtures of asphaltenes and resins were measured with vapour pressure osmometry. Precipitation from the same mixtures dispersed in solutions of toluene and pentane were also measured. The data were modelled with previously developed self‐association and precipitation models. Model results with asphaltenes and resins characterized as a single distribution and as individual components are compared. The data and the modelling suggest that asphaltenes and resins are better characterized as a single distribution of self‐associating components.     

Influence of copolymerisation on fracture behaviour of aliphatic polyketones

High strain rate tensile impact properties of aliphatic polyketone terpolymers were investigated and related to the polymer chain structure. Aliphatic polyketones were used as a model system, by changing the termonomer content and type. Aliphatic polyketone is a perfectly alternating copolymer and the structure was changed with the addition of a few mol% of termonomer: propylene, hexylene and dodecene. Studied were the thermal properties with DSC and DMTA, tensile behaviour, notched tensile impact behaviour, notched Izod properties and the temperature development during deformation. The perfectly alternating copolymer had a melting point of 257 °C, a T_g at 15 °C, a high crystallinity (48%), a high yield stress (77 MPa) and yield strain (31%) but a relatively low fracture strain (85%) and an impact strength (notched Izod) of 13 kJ/m². Increasing the propylene content to 6%, lowered the melting temperature to 224 °C, without changing the T_g. The modulus and yield stress were lowered but the impact strength improved. Increasing the length of the termonomer while keeping the T_m at 224 °C lowered the T_g, the modulus, the yield stress but strongly improved the impact resistance. The longer termonomers, with a lower yield stress, reduced the necking behaviour. The temperature increase in front of the notch was about 85 °C. By adding termonomers to aliphatic ketones, the notched impact behaviour improved significantly at the cost of modulus and yield stress.     

Synthesis of boronate-containing copolymers of N,N-dimethylacrylamide, their interaction with poly(vinyl alcohol) and rheological behaviour of the gels

Cross-linking of polyvinylalcohol (PVA) by boronate-containing copolymer of N,N-dimethylacrylamide (DMAA, 1) was studied and compared to cross-linking of PVA by borate buffers in weakly alkaline solutions. The copolymer of M_w=19,000 g mol⁻¹ containing 9 mol% N-acryloyl-m-aminophenylboronic acid (NAAPBA, 2) was prepared by free radical polymerization of the monomers, exhibiting copolymerization constants r₁=0.84 and r₂=2.2. Due to multipoint interaction of the copolymer with PVA via monodiols, the intermolecular cross-linking required for seven-fold and 10-fold lower boron concentrations as compared to borate buffers of pH 8.6 and 7.5, respectively. In rheological measurements, PVA-copolymer gels exhibited storage moduli (G′_max) comparable to those of PVA-borate gels prepared at 7.5-fold higher boron concentration and the same pH 8.6, what testified to the similar concentration of cross-links in the gels. Therefore, DMAA-NAAPBA copolymer is a more effective cross-linker of PVA than borate. The PVA-copolymer gel exhibited much higher relaxation time (97 s) compared to PVA-borate gels (≤20 s) indicating a longer lifetime of junction zones. The ‘shape stability’ of the gel is suggested to originate in the structure of junctions, containing several boronate-diol complexes, between the macromolecules of PVA and the copolymer.     

Deformation behaviour during cold drawing of nanocomposites based on single wall carbon nanotubes and poly(ether ester) copolymers

Relationships between the macroscopic deformation behaviour and microstructure of a pure (PBT-b-PTMO) block copolymer and a polymer nanocomposite (PBT-b-PTMO + 0.2 wt% SWCNT) were investigated by simultaneous small- and wide-angle X-ray scattering (SAXS and WAXS) during tensile deformation using synchrotron radiation. The Young's modulus was found to be 15% higher for the nanocomposite than for the pure block copolymer as well as the yield strength, while the elongation-to-break was less than a half. This different behaviour can be explained by taking into account the different structural features revealed by SAXS and WAXS and thus considering that SWCNT act as anchors in the nanocomposite, sharing the applied stress with the PBT crystals and partially preventing the flexible, non-crystallisable PTMO chains to elongate.     

Electrochemical behaviour of ZrO2 sol-gel pre-treatments on AA6060 aluminium alloy

ZrO₂ pre-treatments applied with the sol-gel technique are a possible replacement of chromium based pre-treatments on aluminium alloys. The thickness and homogeneity of the films deposited on AA6060 alloy are strongly related to the process parameters like preparation of the surface, number of dips and thermal treatment of the film.ZrO₂ films were prepared using the dip-coating technique in sol obtained from metal-organic precursors in an organic solvent (0.1 M Zr(OBuⁿ)₄ in anhydrous n-butanol with addition of acetic acid as complexing agent). Different layers were applied on AA6060 changing number of dips and thermal treatment (150 °C for 1 h or 250 °C for 4 min). The typical thickness of the deposited layers was in the range 70-180 nm depending on process parameters. The electrochemical behaviour of the pre-treated alloy in diluted Harrison solution (0.05 wt% NaCl + 0.35 wt% (NH₄)₂SO₄) was investigated by means of potentiodynamic polarization, open circuit potential measurements, and electrochemical impedance spectroscopy. In addition, the electrochemical behaviour of ZrO₂ sol-gel films was compared with that of chromatized AA6060 and fluotitanated/fluozirconated AA6060. In order to evaluate the adhesion properties of the films, ZrO₂ pre-treated AA6060, chromatized AA6060 and fluotitanated/fluozirconated AA6060 were painted with a polyester resin and subjected to thermal cycles in 0.05 wt% NaCl. Each thermal cycle consisted of heating the samples at 90 °C, permanence at 90 °C for 6 h, cooling at room temperature and permanence at room temperature for 18 h. Impedance measurements were performed at the end of each cycle.Potentiodynamic polarization curves and impedance spectra indicate that ZrO₂ pre-treatments have similar barrier properties to those of chromatized AA6060. However, no self-healing ability is observed for ZrO₂ films.The barrier properties of ZrO₂ films are strongly dependent on process parameters. In particular, the number of dips determines the amount of defects in the film and its homogeneity. The electrochemical behaviour strongly improves increasing the number of dips in the deposition bath. Thermal aging cycles evidence good adhesion properties for ZrO₂ pre-treatments.     

链转移剂对丙烯腈共聚物熔融性的影响

采用水相悬浮沉淀聚合法,以水和二甲基甲酰胺(DMF)的混合液为悬浮液、过硫酸钾和亚硫酸氢钠为引发剂、异丙醇为链转移剂,丙烯腈与丙烯酸甲酯在一定温度下发生共聚合反应,研究链转移剂用量对聚合反应和产物性能的影响,结果表明:在反应温度为45℃、单体浓度为30 wt%、单体摩尔比AN/MA为90/10、悬浮液组成水/DMF为90/10(wt/wt)、链转移剂用量占单体的4 wt%时,可以得到可熔融的丙烯腈共聚物.