Effects of oligosaccharides on phase transition temperatures and rheological characteristics of waxy rice starch dispersion

BACKGROUND: The creation of starch‐based foods incorporated with functional ingredients such as probiotics is of great current interest in the food industry. This study aimed to investigate the effects of prebiotic oligosaccharides on the phase transition temperatures and rheological characteristics of waxy rice starch dispersions. Four oligosaccharides were applied to the rice starch dispersions: chitooligosaccharides, fructooligosaccharides, isomaltooligosaccharides and xylooligosaccharides. RESULTS: The addition of 125 g kg^?1 oligosaccharides elevated the onset and peak temperatures for gelatinisation of 200–400 g kg^?1 waxy rice starch dispersions. The temperature of the storage modulus (G′) for gelatinisation increased markedly on adding fructooligosaccharides to 200–300 g kg^?1 waxy rice starch. For gelatinisation of 300 g kg^?1 rice starch dispersion the effectiveness of the oligosaccharides in changing the above parameters was as follows: chitooligosaccharides > fructooligosaccharides > isomaltooligosaccharides > xylooligosaccharides. Moreover, their effectiveness was dependent on the amylose content, as illustrated by comparing waxy and non‐waxy rice starches (amylose contents 9–256 g kg^?1). Importantly, the logarithmic G′₉₅ change was linearly and negatively correlated with amylose content. CONCLUSION: The results suggest that oligosaccharide‐containing rice starch dispersions may potentially be used for the formulation of oligosaccharide‐containing starchy functional foods owing to the rheological changes of these starch dispersions. Copyright © 2011 Society of Chemical Industry     

BUBBLE TEMPERATURES OF THE BINARY MIXTURES OF 1,2-DIMETHYLBENZENE WITH 2-PROPANOL, 1-BUTANOL, 2-BUTANOL, 2-METHYLPROPAN-1-OL AND 2-METHYLPROPAN-2-OL AT 95 kPa

Bubble temperatures at 95 kPa over the entire composition range are measured for the five binary systems formed by 1,2-dimethylbenzene with 2-propanol, 1-butanol, 2-butanol, 2- methylpropan-1-ol, and 2-methylpropan- 2-ol. A Swietoslawski - type ebulliometer was used for the measurements. The composition versus temperature measurements are well represented by the Wilson model.     

Kinetics of the thermal decomposition of green alga Ulva by thermogravimetry

In this article, we present the findings of our study into the thermal decomposition of the alga Ulva, which can cause serious problems due to its proliferation in certain seas. Its use as a human foodstuff or other similar applications is limited; however, it could be used as a filling or reinforcement material in the manufacture of composite materials. Since the production processes of such materials usually require heating, the thermal stability of this polymeric material needs to be known, and this is the objective of this work. For this reason, we have studied the thermal decomposition in an air atmosphere using thermogravimetry (TG). On the one hand, we evaluated the thermal stability temperatures of the seaweed; and on the other, we determined the kinetic parameters of the alga's two main decomposition reactions, using an n‐order integral kinetic model. It was, therefore, necessary to calculate the best order of reaction. Finally, we determined a series of characteristic temperatures related to the beginning and the end of each of the thermal decomposition reactions. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1913–1922, 2004     

Synthesis of the Silver Nanofluid by ASNSS Process

Arc Spray Nanoparticle Synthesis System (ASNSS) has been used to prepare the silver nanofluids in this study. The metal electrodes under the electrical discharge will melt and evaporate rapidly and condense to form the nanoparticles in the dielectric fluid at lower temperature and produce the suspended nanoparticle fluid. Thus, the mechanism of the ASNSS process is superheating the electrodes by plasma to form metallic nuclei and supercooling these nuclei by dielectric liquid to produce nanofluid. This study considers the different controlling parameters such as discharge current,discharge voltage, pulse-duration time, electrode diameter, and the temperature of dielectric liquid. The optimally operated parameters can be obtained to produce the finer particle size in nanofluid. The results indicate the silver electrodes in alcohol fluid will produce the spherical nanosilver particles. The mean particle size of silver in different dielectric liquid temperatures of-40, -20, 0, and 10℃ is about13.4, 15.8, 17.5, and 21.6 nm, respectively. This indicates that the well suspended fluid can be obtained by controlling the lower dielectric fluid temperature.     

Ultradrawing properties of ultrahigh‐ molecular‐weight polyethylene/carbon nanotube fibers prepared at various formation temperatures

The influence of formation temperature on the ultradrawing properties of ultrahigh‐molecular‐weight polyethylene/carbon nanotube (UHMWPE/CNT) fiber specimens is investigated. Gel solutions of UHMWPE/CNT with various CNT contents were gel‐spun at the optimum concentration and temperature but were cooled at varying formation temperatures in order to improve the ultradrawing and tensile properties of the UHMWPE/CNT composite fibers. The achievable draw ratio (D_ra) values of UHMWPE/CNT as‐prepared fibers reach a maximum when they are prepared with the optimum CNT content and formation temperature. The D_ra value of UHMWPE/CNT as‐prepared fibers produced using the optimum CNT content and formation temperature is about 33% higher than that of UHMWPE as‐prepared fibers produced using the optimum concentration and formation temperature. The percentage crystallinity (W_c) and melting temperature (T_m) of UHMWPE/CNT as‐prepared fiber specimens increase significantly as the formation temperature increases. In contrast, W_c increases but T_m decreases significantly as the CNT content increases. Dynamic mechanical analysis of UHMWPE and UHMWPE/CNT fiber specimens exhibits particularly high α‐transition and low β‐transition, wherein the peak temperatures of α‐transition and β‐transition increase dramatically as the formation temperature increases and/or CNT content decreases. In order to understand these interesting drawing, thermal and dynamic mechanical properties of the UHMWPE and UHMWPE/CNT as‐prepared fiber specimens, birefringence, morphological and tensile studies of as‐prepared and drawn fibers were carried out. Possible mechanisms accounting for these interesting properties are proposed. Copyright © 2010 Society of Chemical Industry     

Thermal conductivity of highly porous Si in the temperature range 4.2 to 20?K

We report on experimental results of the thermal conductivity k of highly porous Si in the temperature range 4.2 to 20 K, obtained using the direct current (dc) method combined with thermal finite element simulations. The reported results are the first in the literature for this temperature range. It was found that porous Si thermal conductivity at these temperatures shows a plateau-like temperature dependence similar to that obtained in glasses, with a constant k value as low as 0.04 W/m.K. This behavior is attributed to the presence of a majority of non-propagating vibrational modes, resulting from the nanoscale fractal structure of the material. By examining the fractal geometry of porous Si and its fractal dimensionality, which was smaller than two for the specific porous Si material used, we propose that a band of fractons (the localized vibrational excitations of a fractal lattice) is responsible for the observed plateau. The above results complement previous results by the authors in the temperature range 20 to 350 K. In this temperature range, a monotonic increase of k with temperature is observed, fitted with simplified classical models. The extremely low thermal conductivity of porous Si, especially at cryogenic temperatures, makes this material an excellent substrate for Si-integrated microcooling devices (micro-coldplate).

PACS

61.43.-j; 63.22.-m; 65.8.-g     

Nanocrystalline Nd2O3: Preparation,phase evolution,and kinetics of thermal decomposition of precursor

Nd₂O₃ was synthesized by calcining Nd₂(C₂O₄)₃·10H₂O in air. The precursor and its calcined products were characterized by thermogravimetry and differential scanning calorimetry, Fourier transform infrared spectroscopy, X-ray powder diffraction, and scanning electron microscopy. The results showed that high-crystallized Nd₂O₃ with hexagonal structure was obtained when the precursor was calcined at 1223 K in air for 2 h. The crystallite size of Nd₂O₃ synthesized at 1223 K for 2 h was about 48 nm. The thermal decomposition of the precursor in air experienced three steps, which are first, the dehydration of 10 crystal water molecules; then, the decomposition of Nd₂(C₂O₄)₃ into Nd₂O₂CO₃; and last, the decomposition of Nd₂O₂CO₃ into hexagonal Nd₂O₃. Based on the KAS equation, the values of the activation energies associated with the thermal decomposition of Nd₂(C₂O₄)₃?10H₂O were determined.     

卡尔费休法测定原油中的水分相关问题的讨论

本文通过实验对比发现新鲜甲醇做为溶剂标定卡尔费休试剂时会使测定值偏高,并对其产生的原因进行了分析。对可能影响实验结果的实验条件,如搅样时间、速率、卡氏炉进样的温度等进行了对比实验,对其结果产生的原因进行了阐述。对pH值、反应速率对实验的影响给出了简单适用的判断和控制方法。     

一种耐温耐盐类凝胶调剖剂封堵性能的研究

高温高盐复杂油藏由于地层温度高,矿化度高,一般堵水剂的可泵时间和长期稳定性达不到使用要求。在实验室研究了一种适用于高温高矿化度复杂油藏深部调剖的凝胶调驱体系,该体系优于传统的凝胶体系,在高温高盐的复杂地层环境下达到了延缓交联和提高凝胶热稳定性的目的。     

Construction of functional aliphatic polycarbonates for biomedical applications

Aliphatic polycarbonates are one important kind of biodegradable polymers and have been commonly used as integral components of engineered tissues, medical devices and drug delivery systems. As far as the biomedical application is concerned, traditional aliphatic polycarbonates usually suffer from the strong hydrophobicity, deficient functionality, and insufficient compatibility with cell/organs. Consequently, the application is quite limited in scope. Due to the imparted appealing properties, aliphatic polycarbonates bearing specifically designed functional/reactive groups attract great interest from researchers in the recent years. The present review outlines the development up to date concerning the design and biomedical application of functional aliphatic polycarbonates, with an emphasis on their ring-opening (co)polymerization preparation.