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聚甲醛的热重分析研究 总被引:4,自引:0,他引:4
由均聚和共聚甲醛在氮气和空气中的热重分析曲线,探讨了聚甲醛的链结构和聚甲醛的各种降解方式同热失重的关系,并利用Coats-Redfern方法计算了共聚甲醛在空气中的动力学参数,对聚甲醛的热稳定性作了讨论. 相似文献
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热分析技术及其在高分子材料研究中的应用 总被引:5,自引:0,他引:5
简要介绍了热分析技术——热重法、差热分析、差示扫描量热法、热机械分析法和动态机械热分析法等及其在高分子材料领域的广泛应用。热分析技术的方法具有快速、方便等优点,在高分子材料的研究中发挥着重要作用。 相似文献
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应用热重分析方法对21种激光打印机用墨粉样品作了热失重研究。在氮气气氛中,分别对21种样品用TA 2050型热重分析仪在静态恒温及动态升温条件下的热稳定性及热解曲线的差异作了比较。在整个静态恒温条件的分析过程中,21个样品的失重在0.60%~1.16%之间,多数在1%左右。从动态升温的热失重数据及其热解曲线可见,各种墨粉之间存在较明显的差异,例如在曲线上呈现单个或多个失重台阶,失重的温度和温度区间的不同以及趋于恒重状态的温度和残重的不同等。据此认为热重分析可以为鉴别不同牌号的墨粉提供依据,而且还可对墨粉的组分作出初步判别。 相似文献
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采用热重法,以氮气为保护气,分别在5、10、15、20℃/min的升温速率下,测得五倍子醛的热重-微分热重(TG-DTG)曲线,并在10℃/min的升温速率下测得样品的差示扫描量热(DSC)曲线。结合热失重数据和五倍子醛结构对其分解机理进行推断和验证,并运用双外推法对五倍子醛的热解动力学进行分析,求得原始状态和热平衡态下的动力学参数。研究结果表明,五倍子醛晶体在升温过程中先经历了非结合水和结合水的受热挥发阶段,然后在163℃之后发生热分解,分子中醛基断裂失去1分子的CO;随着升温速率的升高,五倍子醛的分解反应向高温区域移动,最大失重速率依次减小;热解活化能Eα为286.21 kJ/mol,指前因子lnA为70.21,热解机理函数g(α)=[-ln(1-α)]2/3,反应级数n=2/3;热解活化能随转化率的增加逐渐减小;经动力学参数推断,在室温(25℃)下,五倍子醛的贮存期为4~5年。 相似文献
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热分析联用技术是在热重分析基础上,将多种检测手段并用,准确地研究材料的结构、组成、热反应等特性,从而揭示材料热分解过程本质的技术。在程序升温过程中,利用热分析联用技术对金属材料的质量和热量变化及热分解产物成分等信息进行检测,能更精准地研究金属材料的组成和热分解特性。该文在热重分析法的基础上,着重介绍了其与差热分析、差示扫描量热分析、傅里叶红外光谱分析、质谱分析等分析方法的联用,并以金属材料研究为例,分析了热分析联用技术在金属材料的结构、性能测定等方面的应用,同时展望了热分析联用技术的应用前景。 相似文献
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石油焦与煤混合燃料热重分析研究 总被引:6,自引:0,他引:6
石油焦与煤混合燃烧是高效处理石油焦的有效方法,作者对选用的石油焦和煤不同配比的混合燃料进行了热重分析研究。使用常压高温热天平研究、分析了各配比混合燃料的热解特性和燃烧特性。并根据化学动力学方法计算了各过程的化学动力学参数,即活化能E和频率因子A0。结果表明,各混合燃料热解起始温度大致相同,随煤焦比减小,挥发分析出速率变缓,最大释放速度所对应的温度升高,最终失重率减小,挥发分释放特性指数减小;随煤焦比增大,混合燃料着火温度和燃尽温度逐渐降低,最大燃烧速率所对应的温度降低,燃烧特性指数增大;随煤焦比减小,活化能和频率因子增大。 相似文献
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用热重红外光谱联用技术研究混煤热解特性 总被引:16,自引:4,他引:16
用热重分析仪和傅里叶红外光谱仪,对混煤在惰性气氛中的慢速热解特性进行了动态分析,考察了煤种、掺混比例以及加热速率对热解的影响。结果表明,混煤的热解与单煤的热解有相似之处,热解组分的析出随温度的变化规律一致,但其组分析出量并不是单煤热解析出量的简单叠加。由于掺混煤种间的相互作用,混煤热解气体在析出时间和析出量上均发生了变化。通过对红外吸收光谱的分析,发现混煤热解气体析出规律受掺混煤种的影响很大,高活性煤种的存在会降低混煤热解的初析温度,增加热解气体的析出量,其掺混比例越高,影响也越明显。 相似文献
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Polypropylene (PP)-montmorillonite nanocomposites have been prepared using isotactic PP homopolymers with different rheological properties, and a maleic anhydride grafted PP. Morphology and structure of the composites were investigated by using X-ray techniques (WAXD, SAXS) and transmission electron microscopy (TEM). The absence of pristine clusters of the clay and the presence of intercalated and exfoliated structures were shown for all the investigated samples. The nanocomposite prepared by using maleic anhydride grafted PP showed a widespread exfoliation. The thermal behaviour and degradation have been studied by means of differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The incorporation of the montmorillonite improves the thermal stability in air atmosphere of all the investigated PPs, thanks to a physical barrier effect of the silicate layers. 相似文献
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Caiyu PENG 《大学化学》2018,33(12):12-15
In this paper, the teaching design of Polymeric Characterization Analysis course of Qianjiang College, Hangzhou Normal University was introduced. According to the problems existing in the learning process of independent college students, three measures were adopted. The change of teaching rhythm was proposed, and the sense of accomplishment was improved through case analysis method. Furthermore, the transformation of key points would enhance the cultivation of students' practical ability. These steps would effectively improve students' interestingness in learning and thus optimize teaching efficiency. 相似文献
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A novel energetic microporous metal‐organic coordination polymer {[Ni(tnbpdc)(bpy)(H2O)2] · 1.5(DMF)}n ( 1 ) (tnbpdc = 2, 2′,6, 6′‐tetranitro‐4, 4′‐biphenyl dicarboxylate, bpy = 4, 4′‐bipyridine) was prepared solvothermally and characterized by elemental, IR spectroscopic, and single‐crystal X‐ray diffraction analyses. The X‐ray crystal structure of 1 revealed a rectangular‐shaped grid constructed with tnbpdc linkers and bpy linkers, with the free tunnel size estimated as 11 × 15 Å2. The thermal stability of the compound was evaluated by differential scanning calorimetry and thermogravimetric analysis. Such complexes may find application as novel heat‐resistant energetic materials. 相似文献
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Thermal stability of poly(vinyl chloride)/poly(ethylene oxide) (PVC/PEO) blends has been investigated by thermogravimetric analysis (TGA) in dynamic and isothermal heating regime. PVC/PEO blends were prepared by hot-melt extrusion (HME). According to TG analysis, PEO decomposes in one stage, while PVC and PVC/PEO blends in two degradation stages. In order to evaluate the effect of PEO content on the thermal stability of PVC/PEO blends, different criteria were used. It was found that thermal stability of PVC/PEO blends depends on the blend composition. The interactions of blends components with their degradation products were confirmed. By using multiple heating rate kinetics the activation energies of the PVC/PEO blends thermal degradation were calculated by isoconversional integral Flynn–Wall–Ozawa and differential Friedman method. According to dependence of activation energy on degree of conversion the complexity of degradation processes was determined. 相似文献
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调制式DSC在高聚物研究中的应用 总被引:4,自引:0,他引:4
综述了一种新的热分析技术--调制式差示扫描量热示(Modulated Differentail Scanning Calorimetry)。对其工作原理,优点及在高聚物研究中的应用作了简介。 相似文献
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Methylsilicone resin/polyhedral oligomeric silsesquioxane (POSS) composites with various proportions of POSS monomer were synthesized by the reaction of functionalized TriSilanolIsobutyl-POSS macromonomer with hydroxyl-terminated methylsilicone resin. The structures of the obtained hybrid polymers were characterized with Fourier-transformed infrared (FT-IR) and transmission electron microscopy (TEM). The FT-IR spectra suggested successful bonding of TriSilanolIsobutyl-POSS and methylsilicone resin. TEM analysis showed that POSS can dissolve in methylsilicone resin at the molecular level. The influences of TriSilanolIsobutyl-POSS on the thermal stability and degradation behavior of methylsilicone resin were studied by thermogravimetric analysis (TGA), solid-state 29Si NMR and X-ray photoelectron spectroscopy (XPS). All these techniques showed that TriSilanolIsobutyl-POSS incorporation results in increased decomposition temperatures and oxidation resistance, primarily by reducing the effect of silanol end groups on the thermolysis through condensation reaction of Si-OH groups and partial loss of isobutyl followed by the formation of an inorganic SiO2 layer to prevent methylsilicone from further degradation. 相似文献
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采用无溶剂二氧化碳固态发泡技术,在2.5、3.5、4.0和5.0 MPa饱和压力下制备了泡孔孔径为350-20μm的聚乳酸支架材料.利用热重分析技术、动态热机械分析技术和扫描电子显微镜技术,测定了材料的起始分解温度、分解速率、储存/损耗模量和损耗因子等参数,并利用Kissinger、Ozawa-Doyle和Vyazovkin方程进行了热分解动力学计算,推算了氮气环境下材料的降解时间和使用寿命.结果表明,随着发泡压力的减小,支架材料的泡孔孔径增大,材料的柔韧性增强,表观活化能降低,降解时间缩短. 相似文献