高压下MgO的热弹性研究

利用第一原理平面波赝势方法和广义梯度近似研究了广泛温度和压强范围内MgO的热弹性特性．MgO从低压NaCl到高压CsCl结构的相变压强为397 GPa，表明它在地球内部不会发生相变．在压强上升到150 GPa时，MgO的绝热弹性模量跟0 GPa时的实验值和其他赝势在高压下的计算结果基本一致．从0 GPa上升到20 GPa时，MgO的各向异性逐渐减小；在20?150 GPa时绝对值逐渐增大．MgO明显地违背了Cauchy条件，反应出非中心多体力是重要的．另外，MgO的热力学参量与实验也符合的很好．     

快速热响应复合材料的储/放热性能分析

以膨胀石墨为无机支撑材料、石蜡为有机相变材料,制备出高导热系数和储热密度的快速热响应复合材料,并构建传热性能测试系统对该复合材料的储/放热性能进行研究分析。研究结果表明,复合材料不仅能在熔融状态下保持形状稳定,而且显著提高了在储/放热过程的传热性能,从而有效地解决了传统相变材料高储热密度和低导热系数之间的矛盾。     

石墨烯/石蜡复合材料的热物理性能研究

为改善相变蓄热用石蜡的导热性能,通过向石蜡基材中掺杂微量的石墨烯制备石墨烯/石蜡复合材料。采用扫描电子显微镜、热传导分析仪和差式扫描量热仪等获取了复合材料的表观形貌、热导率、熔点和相变潜热等关键热物性参数,讨论了石墨烯质量分数对这些参数的影响。通过动态热响应实验,揭示了石墨烯质量分数和热源温度对复合材料热响应速率的影响规律。结果表明,与纯石蜡相比,石墨烯/石蜡复合材料的热导率得到显著提高。当石墨烯的质量分数由0.2%升至2.0%,复合材料的热导率由0.266 W·m~(-1)·K~(-1)提高到0.346 W·m~(-1)1·K~(-1)。复合材料的相变潜热与纯石蜡相比并未减小,且其热响应速率高于纯石蜡。     

51 V GaN基高压LED的热分析

设计并制备了51 V高压LED。对器件进行了大电流冲击试验并对器件的损毁原因进行了分析。运用有限元分析软件ANSYS对LED关键结构部位进行参数化建模及热分布模拟,得到其稳态的温度场分布;然后经过与红外热像仪成像图对比,得出电极烧毁的原因在于芯粒连接处的电极过薄过窄而导致的电阻过大,为后续设计更可靠的高压LED提供了参考。对芯片分别进行蓝光及色温5 000 K的白光封装,并分别测量了热阻,涂覆荧光粉的白光灯珠的热阻要比没有涂覆荧光粉的蓝光灯珠高约4℃/W。同时,51 V高压LED的热阻比1 W大功率LED要高,说明高压LED的散热性能比常规LED要差,这可能与高压LED具有深沟槽及众多的互联电极结构有关。     

榍石的冲击高压行为与辐照损伤效应对比研究

高压和辐照这两种极端条件会造成晶体材料的晶体结构发生改变或损伤。以榍石(CaTiSiO_5)为研究对象,利用冲击高压和样品回收技术,探索冲击高压作用后结构的变化规律,并与辐照造成的损伤榍石作对比研究,认识冲击高压与辐照造成榍石结构损伤的异同。研究表明:冲击高压作用下,晶态的榍石出现结构损伤和非晶化,出现类似于榍石的辐照损伤现象,但具体过程和受损的晶体结构有明显不同。具体表现为:X射线衍射、红外和拉曼光谱的特征峰强度减弱,谱线变宽,细节丢失;冲击高压导致晶态榍石拉曼光谱的Ti–O伸缩振动主峰出现红移,与辐照损伤蜕晶化过程出现的蓝移相反。此外,晶胞参数a、b、c和晶胞体积V减小,与辐照损伤过程相反。     

51V GaN基高压LED的热分析

设计并制备了51 V高压LED。对器件进行了大电流冲击试验并对器件的损毁原因进行了分析。运用有限元分析软件ANSYS对LED关键结构部位进行参数化建模及热分布模拟,得到其稳态的温度场分布;然后经过与红外热像仪成像图对比,得出电极烧毁的原因在于芯粒连接处的电极过薄过窄而导致的电阻过大,为后续设计更可靠的高压LED提供了参考。对芯片分别进行蓝光及色温5 000 K的白光封装,并分别测量了热阻,涂覆荧光粉的白光灯珠的热阻要比没有涂覆荧光粉的蓝光灯珠高约4℃/W。同时,51 V高压LED的热阻比1 W大功率LED要高,说明高压LED的散热性能比常规LED要差,这可能与高压LED具有深沟槽及众多的互联电极结构有关。     

重频激光作用下碳纤维/环氧树脂复合材料热损伤规律

 运用热化学分析、扫描电子显微技术等手段,分析了碳纤维增强环氧树脂基复合材料在ms量级重频激光辐照下的损伤形式,研究了峰值功率密度、辐照时间、重复频率和脉冲宽度等对复合材料烧蚀规律的影响。研究结果表明：在激光辐照过程中,复合材料树脂基体在300 ℃开始裂解;由于裂解气体的保护作用,碳纤维不发生氧化,而是在汽化点（3 300 ℃）汽化烧蚀;复合材料热烧蚀率随峰值功率密度和重复频率提高而增大,随辐照时间增加而减小,最终均趋于定值;增加脉冲宽度可以提高辐照区峰值温度,降低碳纤维损伤的功率密度阈值。     

重频激光作用下碳纤维/环氧树脂复合材料热损伤规律

运用热化学分析、扫描电子显微技术等手段,分析了碳纤维增强环氧树脂基复合材料在ms量级重频激光辐照下的损伤形式,研究了峰值功率密度、辐照时间、重复频率和脉冲宽度等对复合材料烧蚀规律的影响。研究结果表明：在激光辐照过程中,复合材料树脂基体在300 ℃开始裂解;由于裂解气体的保护作用,碳纤维不发生氧化,而是在汽化点（3 300 ℃）汽化烧蚀;复合材料热烧蚀率随峰值功率密度和重复频率提高而增大,随辐照时间增加而减小,最终均趋于定值;增加脉冲宽度可以提高辐照区峰值温度,降低碳纤维损伤的功率密度阈值。     

制备Al2O3/Cu复合材料中CuO-Al体系的化学反应

 对CuO-Al粉末预制块经不同温度下反应，测试其温度随时间的变化曲线，利用X射线衍射仪对其反应后的试样进行物相分析，得出产生热爆的反应温度及不同温度下的反应产物。 结果表明，CuO-Al体系反应随介质温度升高，可分为3个不同阶段，温度小于1 200 K，不发生化学反应；温度为1 200~1 473 K时CuO-Al体系发生部分化学反应，其产物为Cu₂O、CuAlO₂ 及Al₂O₃；温度高于1 473 K，CuO-Al体系发生化学反应，其产物为Cu和Al₂O₃，此阶段易出现热爆现象。     

Synthesis and Characterization of a Fluorinated Phenolic Resin/phenolic Resin Blend

Fluorine atoms were introduced into the molecular chain of a phenolic resin (PR) by a two-step acid synthesis process to improve its thermal and hydrophobic properties. The successful synthesis of a fluorinated phenolic resin/phenolic resin blend (F-PR/PR) was proven by Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance 19F (¹⁹F-NMR). The thermal properties of F-PR/PR were analyzed by differential scanning calorimetry (DSC) and thermo gravimetric analysis (TGA) and the results indicate that the F-PR/PR had good thermal stability. The hydrophobic properties of PR were effectively modified as demonstrated by the water drop contact angles. The flexural and tribological properties of F-PR/PR were also investigated. The fluorine atom, by virtue of its electronegativity, size and bond strength with carbon, can be used to create composites from F-PR/PR with remarkable properties. For comparison, two other resin blends were also synthesized.     

Preparation and Thermal Properties of Boron-Containing o-Cresol-Formaldehyde Resin/Octa(aminophenyl)-POSS Nanocomposites

The boron-containing o-cresol-formaldehyde resin (BoCFR) and octa(aminophenyl) polyhedral oligomeric silsesquioxane (OAP-POSS) were synthesized, and the BoCFR/OAP-POSS nanocomposite prepared via an in-situ method. The curing process of the resin was characterized by Fourier transform infrared (FTIR). The thermal properties and dynamic mechanical properties of the nanocomposites were investigated. The results show that the maximal mechanical loss temperature (T_p) increased with increasing OAP-POSS content. When the content of OAP-POSS was 10 wt% the T_p was over 200°C, 27°C higher than the pure BoCFR. The BoCFR/OAP-POSS nanocomposite had better thermal stablitity than the pure BoCFR. The residual weight of the o-cresol-formaldehyde resin was only 6.13 wt% at 600°C. But the residual weight of the pure BoCFR was 55.73 wt% at 600°C, and the residual weights of the BoCFR nanocomposites were all higher than pure BoCFR. The residual weight of the BoCFR nanocomposite was 63.2 wt% at 600°C and 21.83 wt% at 900°C when the OAP-POSS content was 10 wt%. The weight loss of BoCFR/OAP-POSS nanocomposite can be divided primarily into two temperature stages, from 430°C to 550°C and from 550°C to 900°C. The main thermal degradation reaction follows first order kinetics.     

Synthesis and Properties of Polyphenylsilsesquioxane Modified Phenolic Resin by in-situ Polymerization from Phenyltriethoxysilane Precursor

A series of phenolic resin-polyphenylsilsesquioxane (PR-PPSQ) composites were prepared by in situ formation from phenyltriethoxysilane (PTES) precursor during polymerization of the PR. The precursor was firstly hydrolyzed in a solution, and then the sol was added to the PR polymerization system. The structures of the composites were investigated by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and solid-state ²⁹Si nuclear magnetic resonance (Si-NMR). The PPSQs were spherical particles with a diameter of about 3 µm and nearly uniformly dispersed in the matrix, as revealed by scanning electron microscopy (SEM). The influence of PTES content on the thermal behavior of the PR was characterized by thermogravimetric analysis (TGA) in nitrogen and air atmospheres. The results showed that the onset temperature and residual weight of the composite containing 20 wt% PTES content were improved by 47°C and 8.4%, respectively, compared to the pure PR. The thermal oxidative stability was also greatly increased; the 50 wt% weight loss temperature rose from 567°C for PR to 601°C. The flexural strength of the composites was improved; in particular, the value of the composite containing 15 wt% PTES content was elevated by 32% (from 41.66 to 55.33 MPa).     

5.5 GPa下碳纳米管的热稳定性研究

 利用X射线衍射和透射电子显微镜研究了碳纳米管在5.5 GPa下的热稳定性问题。根据以往的研究在常压真空条件下碳纳米管的热稳定性非常好，其结构在2 800 ℃以下可能并不发生变化。实验中发现，虽然在5.5 GPa压力下冷压作用后碳纳米管的微结构没有明显的改变，但在950 ℃既开始发生改变，转变成类巴基葱和类条带结构，而在1 150 ℃其结构转变成石墨结构。高压是这种转变的主要原因，高压可以促使碳纳米管管结构的破裂，从而减小了它的热稳定性。     

高压烧结镀Cr、Ti膜金刚石/铜复合材料热导率研究

 采用磁控溅射方法,在金刚石表面镀覆活性金属Cr膜和Ti膜,在高温高压下合成了镀活性金属膜金刚石/铜复合材料。实验发现,活性金属的加入增强了金刚石与铜界面间的结合强度,减少了界面热阻,提高了复合材料的热导率。复合材料热导率随着金刚石体积分数的增加而降低,随着金刚石的粒度增大而提高。这主要是由界面热阻引起的,可以通过增大金刚石粒度和改善界面状态来提高复合材料热导率。     

高压与加热协同处理对牛肌肉中蛋白酶活性的影响

在不同温度(20～60℃)和压力(0.1～600 MPa)下处理20 min,对牛肌肉中蛋白酶活性的影响进行了研究.结果显示:室温下,随着处理压力的增加,酶的活力显著下降,而压力达400 MPa及以上时,酶的活力则没有明显变化,同时在pH值为3和7.5时酶的活性几乎完全丧失.200 MPa以下的压力处理使肌肉中游离氨基...     

高压热处理对铝青铜热物理性能的影响

在5 GPa压力下对铝青铜进行750℃、保温15 min的高压热处理,对高压热处理前后铝青铜的电导率以及25～600℃温度范围内的热扩散系数、热容和热导率进行测试,结合显微组织的观察结果,探讨了高压热处理对铝青铜热物理性能的影响。研究表明:高压热处理能增大铝青铜的热扩散系数,减小热容;对热导率而言,温度低于400℃时高压热处理能增大铝青铜的热导率,而温度高于400℃时高压热处理能减小铝青铜的热导率。分析认为,产生变化的主要原因是高压热处理使铝青铜的微观组织发生了变化。     

The Mechanical Properties,Compatibility, and Thermal Stabilities of POE-Graft-Methyl Methacrylate and Acrylonitrile(POE-g-MAN)/ Styrene-Acrylonitrile Copolymer (SAN Resin) Blends

POE-graft-methyl methacrylate and acrylonitrile (POE-g-MAN) was prepared by graft copolymerization of methyl methacrylate (MMA) and acrylonitrile (AN) onto polyethylene-octene copolymers (POE) with suspension polymerization. POE-g-MAN/SAN resin blends (AOMS) were prepared by blending POE-g-MAN with styrene-acrylonitrile copolymer (SAN resin). The mechanical properties, compatibility, and thermal stabilities of AOMS were studied. The notched impact strength of the blends reached 54.0 kJ/m² when the AN/(MMA + AN) ratio (f_AN) of POE-g-MAN, benzoyl peroxide dosage, and POE content in AOMS were 15 wt%, 1.0 wt%, and 25 wt%, respectively. Transmission electron microscopy analysis showed that the highest toughness occurred when the size of POE-g-MAN particles and the surface-to-surface inter-particle distance were proper. Scanning electron microscopy analysis indicated that the AOMS fracture surface had plastic flow visible, which looked like a fibril morphology when the AN/(MMA + AN) ratio (f_AN) of POE-g-MAN was 15 wt%. The toughening mechanism of AOMS was shear yielding of the matrix, which endowed AOMS with remarkable toughness. Dynamic mechanical thermal analysis showed that the compatibility of the POE phase and SAN phase improved after graft copolymerization of MMA and AN onto POE. When the grafting chain polarity was appropriate, the miscibility between POE-g-MAN and SAN resin was the best. Thermogravimetry analysis showed that thermal stability of AOMS increased with increasing AN units in POE-g-MAN.     

Thermal Stability and Degradation Kinetics of Poly(Methyl Methacrylate)/Sepiolite Nanocomposites by Direct Melt Compounding

Poly(methyl methacrylate) (PMMA) nanocomposites based on sepiolite modified with trimethyl hydrogenated tallow amine by an adsorption process were prepared by melt compounding using a corotating twin screw extruder. The morphology and dispersion of sepiolite in the PMMA were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Thermal stability and the activation energies were investigated by thermogravimetric analysis/differential thermogravimetric (TGA/DTG). The XRD and TEM results show that the sepiolite was dispersed homogeneously in the PMMA matrix at a nanometer scale. The TGA analysis revealed that the addition of sepiolite improved the thermal stability of PMMA. The apparent activation energies were calculated by the method of Flynn–Wall–Ozawa in nitrogen at four different heating rates, showing that sepiolite increased the apparent activation energies by about 20 kJ/mol within the degree of conversion (α) of 0.35–0.9, as compared with the reference PMMA sample.     

Mechanical,Thermal, and Rheological Properties of EPDM-graft-methyl Methacrylate and Styrene (EPDM-g-MS)/Methyl Methacrylate-Styrene Copolymer (MS Resin) Blends

EPDM-graft-methyl methacrylate and styrene (EPDM-g-MS) were synthesized by solution graft copolymerization of methyl methacrylate (MMA) and styrene (St) onto ethylene-propylene-diene terpolymer (EPDM). EPDM-g-MS/MS resin blends (MES) tht were prepared by melt blending EPDM-g-MS and methyl methacrylate-styrene copolymer (MS resin). The mechanical properties, compatibility, thermal stabilities and rheological properties of MES were studied by the pendulum impact tester and the tension tester, differential scanning calorimetric (DSC), thermogravimetry analysis (TGA), and the capillary rheometry, respectively. The results showed that EPDM-g-MS had an excellent toughening effect on MS resin; the notched Izod impact strength of MES reached 20.7 kJ/m² when EPDM content in MES was 25 wt%, about 14 times that of MS resin. EPDM-g-MS and MS resin were partially compatible, and the compatibility increased with an increasing MMA/St ratio of EPDM-g-MS. MES had excellent heat-resistance, which increased as the EPDM content in MES and MMA/St ratio of EPDM-g-MS rose. MES melt flow confirmed pseudoplastic flow characteristics. The apparent viscosity (η _a ) of MES decreased with an increasing shearing rate (γ) and temperature, but increased with an increasing EPDM content in MES and MMA/St ratio of EPDM-g-MS. The flow activation energy of MES was lower than that of MS resin.