SiO2 溶胶不同掺杂方式对含氟聚丙烯酸酯/SiO2 杂化涂层性能的影响

用酸催化溶胶-凝胶法制得SiO2溶胶,分别采用共混法和原位聚合法制备含氟聚丙烯酸酯/SiO2纳米杂化涂层.利用红外光谱、扫描电镜等表征了杂化涂层的结构、形态及SiO2相的分散性;研究了SiO2含量、分布和界面状况等与杂化涂层的表面性能和力学性能的关联与影响.结果表明,SiO2在两种方法制备的杂化涂层中均以Si-O网络的形式存在,原位聚合法中SiO2相的分散性优于共混法;含氟聚丙烯酸酯涂层中引入SiO2相后,涂层性能明显提高,共混法的疏水性优于原位聚合法;二者的力学性能随SiO2相含量变化的趋势相同,原位聚合法略优于共混法.     

纳米SiO_2增韧改性环氧乙烯基酯树脂的性能研究

为了对环氧乙烯基酯树脂(EVER)进行增韧改性,采用KH570硅烷偶联剂对纳米SiO2进行表面处理,考察了纳米SiO2表面改性及其质量分数对EVER力学性能的影响。经过偶联剂处理的纳米SiO2复合材料在树脂基体中具备更好的分散性和相容性,力学性能明显优于纯EVER材料和未经偶联剂处理的复合材料。纳米SiO2质量分数为3%时,纳米SiO2复合材料的拉伸强度、断裂伸长率、冲击强度分别比纯EVER材料提高了42.10%,43.38%和91.91%;纳米SiO2质量分数为4%时,纳米SiO2复合材料的拉伸模量比纯EVER材料提高了34.57%。通过观察冲击断面的SEM照片,分析了纳米SiO2增韧改性的作用机理。结果表明:纳米SiO2增韧改性的关键在于诱发基体产生银纹,使其对裂纹扩展起到钝化、阻碍的作用。     

POSS改性AFG-90环氧树脂体系流变特性

对新型有机-无机杂化纳米材料多面体低聚硅倍半氧烷(POSS)改性AFG-90环氧树脂体系前后的粘度变化进行研究,并根据双Arrhenius方程建立了与试验数据较为符合的化学流变模型,同时以此模型对改性树脂体系RTM工艺性能进行评估.     

纤维增强SiO2气凝胶隔热复合材料的制备及其性能

将无机陶瓷纤维与SiO2溶胶混合,经超临界干燥制备了SiO2气凝胶隔热复合材料。SiO2气凝胶纤细的骨架颗粒减少了固态热传导,纳米级孔减少了气体热传导和对流传热,同时无机陶瓷纤维减少了辐射传热。SiO2气凝胶复合材料具有良好的隔热性能,其200℃和800℃的热导率分别为0.017W/m.K和0.042W/m.K。纤维的加入提供了力学支撑,高温处理增强了气凝胶骨架强度,材料在常温和高温下均具有良好的力学性能,其常温的拉伸、弯曲和抗压强度分别为1.44MPa、1.31MPa和0.98MPa(10%应变),800℃的拉伸、弯曲和抗压强度分别为1.95MPa、1.80MPa和1.42MPa(10%应变)。     

(CH3)2SiCl2和N2H4 反应产物为先驱体制备Si/C/N纳米微粉

采用(CH3)2SiCl2和N2H4反应产物为先驱体,在H2、NH3气条件下,用化学气相裂解法制备出Si/C/N纳米复合微粉这一全新的合成体系.对温度、气体流量,H2/NH3的比例等合成工艺条件对微粉的性质、形貌、组成等的影响进行了较为系统的讨论,并从热力学和动力学的角度初步讨论了产物裂解机理及组成的变化形成机理.所合成的Si/C/N微粉为无定型球状颗粒,N的含量从16.49%～26.75%可调,粒径最小达40 nm.     

不同分散剂对纳米SiO_2水中分散的影响

选取六偏磷酸钠(SHMP)、十二烷基苯磺酸钠(SDBS)及KCl作分散剂,并采用超声分散方法,制备纳米SiO2悬浮液,对纳米SiO2的水中分散性能进行研究。测试分散体系中纳米SiO2粒子的粒径及分布、Zeta电位及透光率,探讨了不同分散剂对纳米SiO2分散性能的影响。结果表明:不同分散剂对纳米SiO2的粒径都有明显影响,但粒径分布宽度差别较大;同在分散粒径较小的条件下,分别添加3种分散剂的悬浮液体系具有不同的稳定性,其中含SDBS的分散体系因静电和空间位阻的作用而表现出良好的分散稳定性。     

有机-无机杂化气凝胶隔热材料的研究进展

针对SiO2气凝胶脆性大、强度低、难以直接工程应用的缺陷,首先综述了基于高分子纤维增强、聚合物交联以及共前驱体法制备的有机杂化SiO2气凝胶的研究现状;然后,分析这三类材料的合成原理、制备工艺和性能;最后,从制备成本、性能调控以及传热与力学增强机理等角度提出未来研究方向。     

纳米SiO2改性聚合物锂离子电池的研究

研究了一种基于含氟聚合物的聚合物锂离子电池,考察了SiO2纳米粉对聚合物电解质隔膜的机械性能、吸液量以及电导率的影响,用电镜分析探讨了纳米改性聚合物电解质膜的微观结构;并以此纳米改性聚合物隔膜组装了小型的聚合物锂电池,研究了其电性能.     

聚硅氧烷/二乙烯基苯的交联与裂解

通过研究聚硅氧烷 (PSO)与二乙烯基苯 (DVB)的交联与裂解发现 ,只有在氯铂酸的催化下 ,PSO与DVB才能完全交联固化。催化剂含量为 11 31ppm、质量比为 1:0 5的PSO DVB体系在 12 0℃下交联 6小时后 ,其陶瓷产率为 76 %。该体系的室温粘度为 10 5mPa·s,与碳纤维 (Cf)的接触角为 34° ,非常适合制备三维纤维编织物增强的陶瓷基复合材料。XRD测试表明 ,在 10 0 0℃下裂解的产物中出现SiO2 微晶 ,12 0 0℃时出现 β -SiC微晶 ,温度再升高 ,两种晶粒明显长大。 10 0 0℃裂解产物中Si、O、C三种原子的含量分别为 38 33wt %、 2 7 33wt %、 34 34wt% ,其中C大部分以自由碳形式存在 ,其余部分与Si、O无序混合 ,形成 [Si (O ,C) 4]结构。这种结构在 12 0 0℃以上转变为 [SiO4]和 [SiC4]结构     

双重改性空心微珠的制备及表征

首先采用液相沉积碳化法对空心微珠表面进行无机改性,制备出表面无机改性空心微珠;再对无机改性空心微珠进行有机改性,制备出了双重改性空心微珠。采用扫描电子显微镜、X射线衍射、红外光谱、热失重以及分光光度计法对双重改性空心微珠的制备进行了表征。结果表明：采用双重改性方法制备的表面改性空心微珠微观形貌仍为球状,微珠由灰黑色变为淡黄色;微珠表面的CaCO3属方解石相六方晶系;双重改性空心微珠中CaCO3质量分数约为7%,有机改性剂质量分数约为17%。双重改性空心微珠较之单纯有机改性空心微珠在500SN基础油中的分散稳定性能明显提高。     

Magnetic,thermal stability and dynamic mechanical properties of beta isotactic polypropylene/natural rubber blends reinforced by NiZn ferrite nanoparticles

The dispersion of magnetic nanoparticles in matrix is crucial to ensure optimum performance of the composite. The difficulty level of achieving good dispersion is further increase when a multi-phases of matrix is present. A pre-coating technique of magnetic nanoparticles with polypropylene using ball-mill prior to melt-blending process was employed to prepare a multi-phases thermoplastic natural rubber composite. The effect of filler loading (2 wt%-10 wt%) on morphology, structure, magnetic properties, thermal stability and dynamic mechanical properties of the composites were investigated. It was found that the NiZn ferrite nanoparticles act as nucleating agent to form beta isostatic polypropylene thermoplastic composites. The composites' magnetic properties are directly dependent on the filler concentration. The dispersion of magnetic fillers in polymer matrix plays role in affecting the magnetic properties and thermal stability. The preference of filler to locate at amorphous phase has distorted the chain orientation of natural rubber and polypropylene. Hence, the polymorphism and crystallinity of the matrix varied as the filler loading increased, affecting the dynamic mechanical properties. It was found that 8 wt% NiZn nanocomposite exhibits highest E’ and tanδ, indicating the dynamic mechanical properties of NiZn nanocomposite are affected by β-phase degree.     

Effect of organo-modified montmorillonite nanoclay on mechanical,thermal and ablation behavior of carbon fiber/phenolic resin composites

The mechanical, thermal and ablation properties of carbon phenolic (C-Ph) composites (Type-I) rein-forced with different weight percentages of organo-modified montmorillonite (o-MMT) nanoclay have been studied experimentally. Ball milling was used to disperse different weight (wt) percentages (0, 1,2,4,6 wt.％) of nanoclay into phenolic resin. Viscosity changes to resin due to nanoclay was studied. On the other hand, nanoclay added phenolic matrix composites (Type-II) were prepared to study the dispersion of nanoclay in phenolic matrix by small angle X-ray scattering and thermal stability changes to the matrix by thermogravimetric analyser (TGA). This data was used to understand the mechanical, thermal and ablation properties of Type-I composites. Inter laminar shear strength (ILSS), flexural strength and flexural modulus of Type I composites increased by about 29％, 12％and 7％respectively at 2 wt.％ addition of nanoclay beyond which these properties decreased. This was attributed to reduced fiber volume fraction (％Vf) of Type-I composites due to nanoclay addition at such high loadings. Mass ablation rate of Type-I composites was evaluated using oxy acetylene torch test at low heat flux (125 W/cm2) and high heat flux levels (500 W/cm2). Mass ablation rates have increased at both flux levels marginally up to 2 wt.％ addition of nanoclay beyond which it has increased significantly. This is in contrast to increased thermal stability observed for Type-I and Type-Ⅱ composites up to 2 wt.％addition of nanoclay. Increased ablation rates due to nanoclay addition was attributed to higher insulation effi-ciency of nanolcay, which accumulates more heat energy in limited area behind the ablation front and self-propagating ablation mechanisms triggered by thermal decomposition of organic part of nanoclay.     

The investigation of NTO/HMX-based plastic-bonded explosives and its safety performance

3-nitro-1,2,4-triazol-5-one (NTO) is the main component of insensitive munitions (IM) formulation because of its outstanding insensitive properties.In this paper,a series of NTO/HMX-based composite explosives were prepared and characterized.The study focuses on the effect of NTO on the performance of the formulations,especially the safety performance.The results revealed that the mechanical sensi-tivity of formulations was associated with NTO content,as well as the thermal conductivity,specific heat capacity and Arrhenius parameters.Then,the high amount of NTO using in formulation was proved to be helpful for NTO/HMX-based formulation to exhibit good thermal safety.Besides,by accelerating rate calorimeter (ARC) and a modified cook-offequipment,the pressure and pressure rise rate were proved as the important indicator for judging the thermal safety performance in confined spaces.Finally,the numerical simulation was used as a credible method for predicting the respond temperature of cook-off experiment.     

Mechanical properties and thermal conductivity of pristine andfunctionalized carbon nanotube reinforced metallic glass composites:A molecular dynamics approach

This work uses the molecular dynamics approach to study the effects of functionalization of carbon nanotubes (CNTs) on the mechanical properties of Cu64Zr36 metallic glass (MG). Three types of functional groups, carboxylic, vinyl and ester were used. The effect of CNT volume fraction (Vf) and the number of functional groups attached to CNT, on the mechanical properties and thermal conductivity of CNT-MG composites was analysed using Biovia Materials Studio. At lower values of Vf (from 0 to 5％), the per-centage increase in Young's modulus was approximately 66％. As the value of Vf was increased further (from 5 to 12％), the rate of increase in Young's modulus was reduced to 16％. The thermal conductivity was found to increase from 1.52 W/mK at Vf=0％to 5.88 W/mK at Vf=12％, thus giving an increase of approximately 286％. Functionalization of SWCNT reduced the thermal conductivity of the SWCNT-MG composites.     

盖板式陶瓷热防护系统的传热性能优化

针对高超声速飞行器对盖板式陶瓷热防护系统的迫切需求,建立了热防护系统结构瞬态传热模型;并研究了防隔热层的物性参数,厚度尺寸,相变层的种类、位置等因素对热防护系统结构传热性能的影响。结果表明,隔热层物性参数及厚度尺寸对热防护系统结构传热性能具有决定性影响,而防热层的物性参数及厚度尺寸几乎不产生影响。相变材料的引入能够明显改善热防护系统结构的传热性能。调整和优化相变层位置是改善热防护系统结构传热性能、降低结构厚度的一个有效途径。隔热层厚度的优化结果可为热防护系统结构设计提供一定的参考和依据。     

具有C轴取向Al3+掺杂型ZnO薄膜的溶胶-凝胶法制备及其性能研究

以乙二醇甲醚为溶剂,采用Sol-Gel法制备出具有C轴取向、可导电的Al3+离子掺杂ZnO透明薄膜,并利用场发射扫描电镜、X-射线衍射、能谱分析、标准四探针和反射光谱仪等对薄膜的组成、结构和光学性能进行了分析.结果表明:Al3+离子掺杂ZnO薄膜为六方纤锌矿型结构,由六棱柱状阵列构成,具有C轴择优取向;薄膜电阻率随Al3+离子掺杂浓度的升高而降低;在可见光区域,薄膜透光率随Al3+离子掺杂浓度的升高而降低,掺杂3％ ZnO薄膜的透光率达到90％左右,禁带宽度为3.25 eV,具备制作薄膜太阳能电池透明导电电极材料的应用价值.     

Formulation development and characterization of cellulose acetate nitrate based propellants for improved insensitive munitions properties

Cellulose acetate nitrate (CAN) was used as an insensitive energetic binder to improve the insensitive munitions (IM) properties of gun propellants to replace the M1 propellant used in 105 mm artillery charges. CAN contains the energetic nitro groups found in nitrocellulose (NC), but also acetyl functionalities, which lowered the polymer's sensitivity to heat and shock, and therefore improved its IM properties relative to NC. The formulation, development and small-scale characterization testing of several CAN-based propellants were done. The formulations, using insensitive energetic solid fillers and high-nitrogen modifiers in place of nitramine were completed. The small scale characterization testing, such as closed bomb testing, small scale sensitivity, thermal stability, and chemical compatibility were done. The mechanical response of the propellants under high-rate uni-axial compression at, hot, cold, and ambient temperatures were also completed. Critical diameter testing, hot fragment conductive ignition (HFCI) tests were done to evaluate the propellants' responses to thermal and shock stimuli. Utilizing the propellant chemical composition, theoretical predictions of erosivity were completed. All the small scale test results were utilized to down-select the promising CAN based formulations for large scale demonstration testing such as the ballistic performance and fragment impact testing in the 105 mm M67 artillery charge configurations. The test results completed in the small and large scale testing are discussed.     

Liquid phase in-situ synthesis of LiF coated boron powder composite and performance study

Among practical metal additives, boron (B) has a high volumetric heating value, making it a promising choice as a fuel additive. Although B can theoretically yield a large amount of energy upon complete combustion, its combustion is retarded by the initial presence of B oxide, which coats the surfaces of B particle. To improve the ignition and combustion properties of B powder, LiOH and NH₄F were used as precursors to synthesize uniformly LiF-coated B composites (LiF-B) in situ. The LiF-B mixture was also prepared for comparison using a physical method. X-ray diffraction (XRD), Fourier-transform infrared (FTIR), scanning electron microscope (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used to characterize the morphologies and compositions of the products. The thermal and combustion properties of the samples were characterized by thermal gravity-differential thermal gravity (TG-DTG), differential scanning calorimetry (DSC) and closed bomb experiment. The XRD, FTIR, SEM and EDS results demonstrated the successful preparation of the coated LiF-B sample. The TG-DTG and closed bomb experiment results indicated that the addition of LiF decreased the ignition temperature of B powder, and increasing its reaction efficiency. DSC results show that when LiF-B was added, the released heat of underwater explosive increased by 6727.2, 7280.4 and 3109.6 J/g at heating rates of 5, 10, and 15 °C/min, respectively. Moreover, LiF-B decreased the activation energy of secondary combustion reaction of explosive system as calculated through Kissinger's method by 28.9%, which indicated an excellent catalytic effect for the thermal decomposition of underwater explosive. The results reveal that LiF can improve the combustion efficiency of B powder, thereby increasing the total energy of explosives. The mechanical sensitivity increased slightly after adding LiF-B to the underwater explosive. Compared to the underwater explosive with added B, the mechanical sensitivity of the explosive with added LiF-B was significantly lower.