纳米ZnO／石蜡复合相变材料的热物理性质研究

本文通过将纳米氧化锌（ZnO）颗粒加入熔融的石蜡（PW）并进行搅拌和超声制备了一种纳米ZnO／PW复合相变储能材料。为使纳米氧化锌在基体物质中分散均匀,在制备过程中使用了搅拌和超声以制备均匀的复合材料。使用扫描电镜观察其微观结构表明氧化锌在石蜡中分散良好。对所得ZnO／PW复合相变材料的相变温度、相变焓及导热系数等热物...     

Effect of Ultrafine Full-Vulcanized Powdered Rubber on the Properties of the Intumescent Fire Retardant Polypropylene

Ultrafine full-vulcanized powdered rubber (UFPR) was added into intumescent fire retardant polypropylene (IFR-PP) composites, and fire retardance, morphology, and properties of the composite were analyzed. Ammonium polyphosphate and pentaerythritol were used as the intumescent fire retardants (IFR). The mechanical properties (elongation at break increased from 70% to 110%) and the melt flowability of IFR-PP improved by adding a small quantity of UFPR (less than 0.5 phr) but decreased when the UFPR was more than 0.5 phr. At the same time, the fire retardance, as measured by the limiting oxygen index and the UL94 vertical test rating, and other mechanical properties decreased appreciably with adding UFPR. The reasons were analyzed by using SEM micrographs, and a model was proposed to explain the reasons.     

Effect of Modified Intumescent Flame Retardant via Surfactant/Polyacrylate Latex on Properties of Intumescent Flame Retardant ABS Composites

In order to prepare intumescent flame retardant acrylonitrile-butadiene-styrene (ABS) composites with only a small decrease in their mechanical properties, we investigated the effect of adding an elastomeric polyacrylate latex and the surfactant TX-10 phosphate to modify the ammonium polyphosphate, melamine, and calcium 3-hydroxy-2, 2-bis(hydroxymethyl) propyl phosphate normally used, which resulted in an intumescent flame retardant composite (IFRC) powder with the aim of improving compatibility. These ABS/IFRC composites were compared with standard material containing unmodified intumescent flame retardant (NIFR) by investigating their thermal properties, melt characteristics, mechanical properties, and microstructure. The data showed that the glass transition temperature of the ABS/IFRC composites decreased slightly in all cases, the complex viscosity of the ABS/IFRC composites was remarkably reduced, and the mechanical properties improved in comparison with the material containing NIFR. A slight increase in impact strength retention, as well as a remarkable increase in tensile and flexural strength retention of ABS/IFRC, was achieved due to superior compatibility between ABS and IFRC in comparison with ABS/NIFR.     

Experimental Study on Heat Transfer of Intumescent Fire Retardant Polypropylene Materials

Intumescent fire retardant polypropylene (IFR-PP) materials, primarily comprising polypropylene, ammonium polyphosphate (APP), pentaerythritol (PER), and polyamide-6, were prepared. The burning behavior of IFR-PP materials was measured using a cone calorimeter. The heat transfer processes for IFR-PP materials were studied using a cone calorimeter and a multi-channel data acquisition instrument. The temperature distribution results inside IFR-PP materials indicated that the temperature measured near the top surface of the sample was much higher than the temperature at far from the top surface. The external temperature field measurement results for IFR-PP samples showed that the temperature rose gradually with time before the intumescent char was formed. Then the temperature values of the sample decreased sharply due to the formation of char cap and accumulating gases. The heat transfer processes of IFR-PP materials were also affected by the difference in formulations such as changes in the contents of APP and PER.     

Combined Infrared Thermal Imaging and Laser Heating for the Study of Materials Thermophysical and Processing Properties at High Temperatures

Focused laser irradiation can easily drive materials to extreme temperatures with very high precision and control. In combination with infrared imaging and material characterization techniques, the resulting thermal load can be assessed to derive meaningful thermophysical properties avoiding interferences that would normally occur with direct contact measurements of temperature. In this focused article we first address technical challenges with the experimental implementation involved in obtaining laser-induced temperature field data from infrared imaging. We then discuss suitable heat transport models for analysis of thermal data and, finally, describe specific examples of thermophysical material parameters derived from combined infrared imaging and laser heating. The aim is to illustrate general principles of this combined laser-based heating and IR thermal imaging approach that are useful for experimentation under extreme conditions, which often remain out of reach of conventional methods.     

Simulated Effects of Physical Parameters on Heat Transfer of Intumescent Fire-Retardant Polypropylene during Burning

Physical properties of intumescent materials are important parameters as input data in modeling the combustion behavior of intumescent materials in a fire. In this paper, effects of important physical properties on heat transfer of intumescent materials during burning are simulated based on a combustion model of intumescent fire-retardant polypropylene (IFR-PP) materials. Physical properties selected are thermal conductivity of virgin material and char layer, specific heat capacity of virgin material, density of virgin material, surface emissivity of virgin material and char layer, and intumescent temperature. Predicted temperature curves at a location 9 mm from the bottom of the IFR-PP material at an incident heat flux of 50 kW/m² are shown for the varied physical parameters values. The results show that these varied parameter values can affect the heat transfer of materials remarkably.     

Effect of Polyborosiloxane on the Flame Retardancy and Thermal Degradation of Intumescent Flame Retardant Polypropylene

A novel synergistic flame retardant agent containing boron and silicon, namely polyborosiloxane (PBSil), was prepared via the condensation reaction of boric acid (BA), tetraethoxysilane (TEOS), and octamethyl cyclotetrasiloxane (OMCTS). The obtained PBSil was then combined with an intumescent flame retardant (IFR) to flame retard polypropylene (PP), and the effects of PBSil on the flame retardancy and thermal degradation of the PP/IFR composite were investigated. It was found that PBSil could improve the compatibility between the IFR and the PP matrix, thereby improving the mechanical properties of the composite. Compared with zinc borate, zeolite, and nano-silica, PBSil showed much better flame retardancy and smoke suppression in the PP/IFR composite. When the content of PBSil was 3.0 wt%, the limiting oxygen index (LOI) value of the flame retardant PP was increased from 29.0% to 35.0%, and the UL-94 rating was improved from V-1 to V-0 rating. Simultaneously, the heat release rate (HRR) and smoke production rate (SPR) of the composite were decreased dramatically. The thermogravimetric (TG) analysis, Fourier transform infrared (FTIR), and thermogravimetry-Fourier transform infrared spectrometry (TG-FTIR) results showed that, PBSil could enhance the thermostability of the IFR, and promote the char formation. Furthermore, the compactness and thermostability of the intumescent char were significantly improved, contributing to the improvement of the flame retardancy of the composite.     

苯低压热解的光电离质谱和动力学模型 (cited: 3)

研究苯在30 Torr和1360～1820 K下的热解过程．利用同步辐射真空紫外光电离质谱技术对热解产物进行了检测,并对其随温度变化的摩尔分数曲线进行了测量．建立了一个低压苯热解动力学模型,并结合生成速率分析展示了燃料分解和芳烃生长过程中的主要反应网络．结果显示苯的分解主要通过氢提取反应生成苯基进行,部分通过单分子解离反应生成丙炔基或苯基进行,并终止于乙炔、丁二炔及1,3,5-己三炔等具有高热稳定性的聚炔烃类物种的生成．此外,低压苯热解中的芳烃生长过程起始于苯和苯基,并主要受到偶数碳增长机理控制．这是由于奇数碳增长机理所依赖的C5和C7物种在低压苯热解中很难生成．     

Effect of an Ultrahigh Rubber ABS Impact Modifier Resin on Mechanical Properties of Intumescent Flame-Retardant ABS Composites

The effect of an ultrahigh rubber acrylonitrile-butadiene-styrene (ABS) impact modifier resin (UHR-ABS) on the mechanical properties of an intumescent flame-retardant ABS composite was characterized. Samples were obtained by compounding ABS and an intumescent flame-retardant master batch that was prepared using an intumescent flame-retardant composite (IFRC) with ABS and/or UHR-ABS as well as by direct compounding IFRC, UHR-ABS, and ABS. The incorporation of UHR-ABS resulted in reduction in the storage modulus, damping behavior and glass transition temperature, as evidenced by dynamic mechanical analysis. With increasing mass fraction of the UHR-ABS, the tensile strength and the flexural strength decreased gradually, and the notched impact strength increased, but the increase was more significant for compounding IFRC, UHR-ABS, and ABS than for compounding ABS and IFRC master batches. SEM micrographs of the fresh fracture surface of the composites were used to estimate the mechanism of the increased notched impact strength owing to the incorporation of UHR-ABS.     

Effect of Heat Treatment on the Mechanical and Tribological Properties of Polyphenylene Sulfide Fiber Materials

Polyphenylene sulfide (PPS) fiber materials, whose raw fibers had been heat treated previously for 1 to 5 days, were prepared by a hot-pressing method. The tribological properties of PPS resin and fiber materials against an AISI 1045 steel ring were evaluated using a block-on-ring wear tester. The results showed that the sample whose raw fibers had been heated at 240°C for 1 day (S1) exhibited the highest impact strength as well as the lowest friction coefficient and wear rate. The friction coefficient of S1 was 39% lower than that of the PPS resin material, and its wear rate was 1 to 2 orders of magnitude lower than those of the other samples. DSC analysis results indicated that the condensed structure of the samples gradually changed from the crystalline to the amorphous state with the increase of heat-treatment time of the raw fibers. DMA and DSC analysis results proved that severe, oxidative cross-linking reactions occurred when the raw fibers were heated over 3 days. It is concluded that proper heat treatment of the raw fibers is advantageous to improve the degree of crystallinity and appropriate oxidative cross-linking; therefore, the prepared PPS fiber material can exhibit better mechanical and tribological performances.     

Synergistic Effect of Organic Vermiculite on the Flame Retardancy and Thermal Stability of Intumescent Polypropylene Composites

Organic vermiculite (OVMT) prepared from vermiculite (VMT), with high aspect ratio and orderly arranged platelets intercalated by octadecyl trimethyl ammonum bromide (OTAB), was used as a synergistic agent on the flame retardancy of a polypropylene/intumescent flame retardant (PP/IFR) system. The flammability and thermal stability of PP/IFR/OVMT composites were investigated by limiting oxygen index (LOI), UL-94 testing, cone calorimetry tests, and thermogravometric analysis. The results of LOI and UL-94 testing showed that low loading of OVMT improved the flame retardancy and retarded dripping for PP/IFR composites. OVMT, with 1% loading, increased the char residue of PP/IFR composites and could act as an effective additive for improvement in flame retardancy, which was confirmed by the cone data. The char layer morphological structures observed by scanning electron microscopy (SEM) showed that OVMT with 1% loading can promote formation of a continuous and compact intumescent char layer. Raman spectroscopy results indicated that the OVMT or its pyrolytic products led to a decrease in size of the carbonaceous micro-domain during combustion, resulting in formation of more compact charred layers. Thus, OVMT with 1% loading showed a synergistic effect with IFR in the combustion of the PP/IFR composites.     

The Effect of Peroxide Cross-Linking on the Properties of Low-Density Polyethylene

Low-density polyethylene (LDPE) was chemically cross-linked with various amounts of dicumyl peroxide (DCP). The cross-link density, determined by Flory–Rehner theory, showed an increase with increasing DCP. The gel content, densities of cross-linked LDPE, thermal stability, crystallization, melting behavior, and tensile properties were studied. The results showed a new finding about the change of weight loss after cross-linking; with increase in temperature, the weight loss showed an increase below the temperature of about 450°C and then showed a decrease at temperatures from about 450°C to 500°C after being cross-linked. The crystallinity, melting point, crystallization temperature, and elongation at break decreased with the increase in DCP. However, the maximum tensile stress increased with the increase in DCP, and the cross-linked samples showed a rubber-like behavior with no flow.     

Effect of the Rubber Components on the Mechanical Properties and Braking Performance of Organic Friction Materials

Vegetable oil modified phenolic resin (PF) mixed with four kinds of rubber modifiers, i.e., styrene butadiene rubber, styrene butadiene 2-vinyl pyridine rubber, nitrile butadiene rubber, and carboxyl nitrile butadiene rubber (CNBR), were used as matrices for organic friction materials. The mechanical and thermal degradation properties of all of the blends were investigated. Friction and braking tests of the organic friction materials based on the different matrices and reinforced with hybrid fibers were carried out. The results showed that the resin was most compatible with CNBR; the CNBR/PF blend possessed much higher impact and toughness, and the friction material based on this blend as a matrix exhibited better friction and braking performance. It was concluded that CNBR, the rubber with the most reactive groups, resulted in better mechanical properties of the friction material, and hence optimized the friction, wear and braking performances.     

热解条件对煤焦-CO2和煤焦-H2O气化的影响

采用沉降炉快速热解和管式炉慢速热解的方法制得两种煤焦,通过环境扫描电镜（ESEM）和X射线衍射仪（XRD）分别观察煤焦的形貌结构和测量煤焦的晶体化程度。使用热重在不同的CO₂和H₂O浓度的气氛条件下研究在CO₂浓度和H₂O浓度变化时热解条件对煤焦-CO₂和煤焦-H₂O气化的影响。结果显示对于实验用褐煤,快速热解和慢速热解条件生成的煤焦均以密实型结构焦为主。快速热解和慢速热解条件生成的煤焦的煤焦-CO₂和煤焦-H₂O气化过程均可以通过收缩核模型很好地拟合。煤焦-H₂O反应和煤焦-CO₂反应的反应位并不相同。     

Influence of Degradation of Poly-L-lactide on Mass Loss,Mechanical Properties,and Crystallinity in Phosphate-Buffered Solution

A bulk degradation of poly-L-lactide (PLLA) rectangular bars was studied by incubating them in phosphate-buffered solution at 37°C for different periods. The characteristics of the mass, water uptake, mechanical properties, thermal behavior, and crystallinity of the PLLA samples were investigated. The results indicate that mass loss and water uptake of PLLA increase with increasing time; however, pH value and mechanical strength decrease. The melting temperature, melting enthalpy, and crystallinity of PLLA firstly increase and then decrease with increasing degradation time. There is no new diffraction peak formed with increasing degradation time, which indicates that the degradation could occur in the amorphous regions firstly and then in the crystalline regions.     

Flame Temperature Effect on the Structure of SiC Nanoparticles Grown by Laser Pyrolysis

Small SiC nanoparticles (10 nm diameter) have been grown in a flow reactor by CO₂ laser pyrolysis from a C₂H₂ and SiH₄ mixture. The laser radiation is strongly absorbed by SiH₄ vibration. The energy is transferred to the reactive medium and leads to the dissociation of molecules and the subsequent growth of the nanoparticles. The reaction happens with a flame. The purpose of the experiments reported in this paper is to limit the size of the growing particles to the nanometric scale for which specific properties are expected to appear. Therefore the effects of experimental parameters on the structure and chemical composition of nanoparticles have been investigated. For a given reactive mixture and gas velocity, the flame temperature is governed by the laser power. In this study, the temperature was varied from 875°C to 1100°C. The chemical analysis of the products indicate that their composition is a function of the temperature. For the same C/Si atomic ratio in the gaseous phase, the C/Si ratio in the powder increases from 0.7 at 875°C up to 1.02 at 1100°C, indicating a growth mechanism limited by C₂H₂ dissociation. As expected, X-ray diffraction has shown an improved crystallisation with increasing temperature. Transmission electron microscopy observations have revealed the formation of 10 nm grains for all values of laser power (or flame temperature). These grains appear amorphous at low temperature, whereas they contain an increasing number of nanocrystals (2 nm diameter) when the temperature increases. These results pave the way to a better control of the structure and chemical composition of laser synthesised SiC nanoparticles in the 10 nm range.     

光子晶体光纤弯曲损耗特性研究

对光子晶体光纤的损耗特性进行了分析,并在实验上对两种典型的光子带隙型和全内反射型光子晶体光纤进行了研究.分别对两种不同结构的光子晶体光纤在弯曲半径2~15 mm范围内的损耗进行了测量.与传统光纤损耗实验结果的对比表明,两种光子晶体光纤的弯曲损耗均不明显,具有很强的抗弯曲损耗能力.实验也证实了光子晶体光纤弯曲损耗存在临界弯曲半径,在大于临界半径的情况下,几乎没有弯曲损耗.从结构上分析并证明光子晶体光纤弯曲损耗随填充比(d/Λ)的增加而减小,填充比越高弯曲损耗越小.     

籽晶层对喷雾热分解法生长ZnO薄膜结晶质量和光电性能的影响

通过脉冲激光沉积(PLD)方法在Si(100)衬底上沉积一层高质量的ZnO籽晶层,在籽晶层上进一步采用超声喷雾热分解(USP)法生长ZnO薄膜,研究了籽晶层对ZnO薄膜结晶质量和ZnO/Si异质结光电特性的影响。研究结果表明,在籽晶层的诱导作用下,USP法生长ZnO薄膜由多取向结构变为(002)单一取向,结晶性能得到了显著改善;籽晶层上生长的薄膜呈现出垂直于衬底生长的柱状晶结构,微观结构更加致密。通过研究紫外光照前后ZnO/Si异质结的整流特性,发现引入籽晶层后,反向偏压下异质结的光电响应显著增加,并且在开路状态下出现明显的光伏效应。     

多孔型热致变色材料表面辐射特性研究

分别采用固相反应法和胶晶模板法制备出了块状和多孔型的钙钛矿锰热致变色材料。研究了不同制备工艺对材料居里温度的影响,探讨了不同掺杂比例、表面粗糙度和表面微结构对材料表面辐射特性的影响。结果表明,由于制备工艺不同,两种不同结构钙钛矿锰材料的居里温度相差较大,但其发射率均随温度升高而增大;而在室温以上,多孔材料的发射率明显比块状材料要大。同时,表面粗糙度对材料表面辐射特性的影响较大。     

在线光电离质谱方法研究HUSY选择性中毒对聚丙烯催化热解行为的影响

利用热解-光电离飞行时间质谱方法,在线研究了不同酸性强度的HUSY沸石催化剂对聚丙烯（PP）催化热解的影响.将HUSY以不同程度的氨气毒化处理,得到不同酸强度和酸位点数量的催化剂,在线获得PP与酸性强度不同HUSY在不同热解温度下的光电离质谱图,通过程序升温热解实验,获得PP与酸性强度不同的HUSY经热解后产物随温度升高的变化趋势.结果表明PP热解产物的生成温度、选择性和转化率均与HUSY的酸性有较强关联.