Evaluation of Polyester Resin as a New Compatibilizer for SBR/PVC Blends

A polyester (PE) based on the glycolyzed products of PET was prepared and added in different concentrations to a series of SBR/PVC blends. The addition of the polyester showed that all properties of SBR/PVC blends were improved by incorporation of PE. Highest mechanical strength values were obtained at a polyester concentration of 7.5 phr. Thermal analysis as well as dynamic mechanical properties of SBR/PVC blends after the addition of 7.5 and 10 phr polyester indicated one single glass transition temperature. The dielectric losses (?") were analyzed in the frequency domains in the two terms of Fröhlich related to the Maxwell Wagner effect and the orientation of the aggregates caused by the movement of the main chain. The permittivity (?') values were found to increase by increasing the polyester content. This increase was followed by a decrease in the ?" up to a 7.5 phr polyester content after which no pronounced change was noticed.     

溶剂萃取法回收与处理含DMAc废水的研究

本文研究了用低沸点萃取剂处理和回收含二甲基乙酰胺（DMAc)废水的可行性及工艺条件，经研究表明，在常温20－35℃时，用氯仿萃取二甲基乙酰胺，当溶剂与水相体积比为2：1时，经六级逆流萃取，可将废水中20％（w/w)的二甲基乙酰胺含量降至300mg/L以下。废水的pH值对萃取效率有明显的影响，当废水的pH值较大，即偏碱性对萃取有利。     

包裹法国红色料在陶瓷领域应用的探索

探索包裹法国红色料在建筑陶瓷工业釉料、坯体中应用的工艺技术条件，采用正交实验方法找出包裹法国红色料在陶瓷釉料、外墙砖、地砖中的最佳发色条件：在釉料中一价的钾、钠离子特别利于该色料的发色；二价离子钡较好、钙次之、镁最差；法国红色料在普通熔块中发色不理想，在特制的熔块中发色良好。     

基于支持向量回归的动力电池参数辨识

根据铅酸蓄电池在放电过程中内部电化学反应导致外部电特性变化的特点,提出一种基于支持向量机原理的电解液密度辨识模型。利用支持向量机理论非线性回归的特性,简化测量电解液密度的过程,在恶劣环境下检测动力电池的电解液密度更显其优越性。预测实验表明,采用改进的交叉验证预测模型具有泛化能力强、稳定性好的特点,并且在小样本的条件下能达到预期的辨识精度。     

Dynamics of single-walled carbon nanotube (SWNT)/polyisoprene (PI) nanocomposites in electric and mechanical fields

Relaxation dynamics of single-walled carbon nanotube (SWNT)/polyisoprene (PI) nanocomposites were examined by dielectric relaxation spectroscopy (DRS) and dynamic mechanical spectroscopy (DMS) over a wide range of frequency and temperature. Both functionalized (SWNT-f) and pristine (SWNT-p) nanotubes were used and their effect on dynamics compared. Functionalized (PISF) nanocomposites were characterized by an increase in the time scale of the normal mode process as a consequence of the strong surface interactions between the polymer matrix and the nanotubes. The exact opposite is seen in pristine (PISP) nanocomposites where a decrease in the time scale of the normal mode relaxation is observed and attributed to weaker surface interactions and the effect of confinement on dynamics. The segmental process in PISF or PISP is not affected by the presence of nanotubes. The temperature dependence of the average relaxation time for normal and segmental modes is of the Vogel-Fulcher-Tammann (VFT) type. A good agreement is observed in the time scale of processes measured by DRS and DMS in PISF nanocomposites. In PISP nanocomposites, however, the time scales obtained from DRS and DMS measurements are not in consistently good agreement and an explanation is offered in terms of confinement.     

Two-dimensional correlation relaxometry studies of cement pastes performed using a new one-sided NMR magnet

We present preliminary results of the first NMR T₁-T₂ two-dimensional relaxation correlation experiments performed using a one-sided NMR system in cement based materials. Two-dimensional correlation relaxometry has itself only recently been demonstrated in cement paste where it proved to be a particularly sensitive probe of pore-water dynamics providing direct information on exchange of water between the gel and capillary pore networks. Further to this we have observed differences in the structural development of a selection of cement pastes throughout the early stages of hydration and verified the theoretical frequency dependence of the ratio T₁ / T₂. When coupled with instrumentation developments in one-sided NMR magnets the way is opened to detailed, spatially resolved studies of the development of hydration and porosity in the surface layers (top 50 mm) of cementitious materials. A new magnet, suitable for such applications, is discussed.     

A comparison of concentration-glasses and temperature-hyperquenched glasses: CO2-formed glass versus temperature-formed glass

Prior work from this laboratory has reported anomalous differences in the viscoelastic responses between temperature-jump formed glasses and carbon dioxide pressure-jump or relative humidity formed glasses. In the present work, we investigate the anomalous behaviour further by examining the structural response of an epoxy resin after pre-annealing treatments. In particular, we have measured the volume change of amine-cured diglycidyl ether of bisphenol A after thermal and carbon dioxide pressure (PCO₂) treatments. Our results show that contrary to prior interpretations in the literature, a plasticizer quench is different from a temperature hyperquench. Consistent with our prior work, the CO₂-formed glass is more stable than the temperature-formed glass in spite of the former having a higher excess volume. Our new results show that the stability persists to above the nominal glass temperature, contrary to what happens in a temperature hyperquench.     

An approach for minimizing a quadratically constrained fractional quadratic problem with application to the communications over wireless channels

Studies for the cognitive model are relatively new in the literature; however there is a growing interest in the communication field nowadays. This paper considers the cognitive model in the communication field as the problem of minimizing a fractional quadratic problem, subject to two or more quadratic constraints in complex field. Although both denominator and numerator in the fractional problem are convex, this problem is not so simple since the quotient of convex functions is not convex in most cases. We first change the fractional problem into a non-fractional one. Second, we consider the semi-definite programming (SDP) method. For the problem with m (m≤2) constraints, we use the SDP relaxation and obtain the exact optimal solution. However, for the problem with m (m>2) constraints, we choose the randomization method to gain an approximation solution in the complex case. At last, we apply this method to practical communications over wireless channels with good results.     

Modification of non‐Newtonian flow behavior of aqueous solution of poly(vinyl alcohol) by conducting polypyrrole prepared by in situ polymerization of pyrrole

The rheological behavior of an aqueous solution of poly(vinyl alcohol) (PVA) and polypyrrole (PPY) dispersions prepared by ferric chloride (FeCl₃)‐catalyzed polymerization of pyrrole was investigated at 12°C using a coaxial rotational viscometer. The results show that the addition of a low dose of FeCl₃ to the PVA solution greatly influences its rheology. The prominent shear‐thickening (dilatant) nature of PVA turns significantly pseudoplastic (shear thinning) in the presence of FeCl₃. Polypyrrole‐loaded PVA was obtained in a stable, optically clear dispersion by in situ polymerization of pyrrole in an aqueous PVA solution (5%) using FeCl₃ as the oxidative catalyst at 12°C. The PPY dispersions in aqueous PVA systems having a low loading of PPY and low Fe⁺³ content retain the dilatant character of an aqueous PVA solution; however, for an aqueous PVA system having a relatively high PPY loading and also a high Fe⁺³ content, prominent pseudoplastic (shear thinning) behavior is exhibited. The odd novel rheological patterns exhibited by a PVA solution in the absence and presence of FeCl₃ and the PVA–PPY dispersions containing FeCl₃ under different sets of conditions are explained on the basis of the complexation of PVA by Fe⁺³ and related ions and also as a consequence of some degree of H‐bonding and chemical grafting between the support polymer PVA and the PPY formed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3737–3741, 2004     

1H nuclear magnetic resonance study of polyurethane prepolymers from toluene diisocyanate and polypropylene glycol

Polyurethane prepolymers prepared from toluene 2,4‐diisocyanate, toluene 2,6‐diisocyanate, and polypropylene glycol with a ratio between the isocyanate and hydroxyl groups equal to 2 were analyzed by ¹H nuclear magnetic resonance (NMR) spectroscopy in acetone‐d₆. Different temperatures and concentrations were used. Toluene 2,4‐dimethylurethane and toluene 2,6‐dimethylurethane were synthesized and used as model compounds to assign prepolymers signals. Measurements of spin–lattice relaxation time T₁ by “inversion recovery” experiments were carried out on toluene 2,4‐diisocyanate, toluene 2,6‐diisocyanate, toluene 2,4‐dimethylurethane, toluene 2,6‐dimethylurethane, and polyurethane prepolymers. Differences in T₁ times were used to interpret prepolymers spectra, by means of the strong observed effect on protons due to the presence of adjacent isocyanate groups. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 347–357, 2003