首页> 外文OA文献 >Liquefied Residue of kenaf core wood produced at different phenol kenaf ratio (Analisis baki pencecairan kayu teras kenaf terhasil pada nisbah Fenol-Kenaf yang berbeza)
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Liquefied Residue of kenaf core wood produced at different phenol kenaf ratio (Analisis baki pencecairan kayu teras kenaf terhasil pada nisbah Fenol-Kenaf yang berbeza)

机译:不同酚红麻比制得的洋麻芯材的液化残渣(分析不同酚醛/纳夫纳比制得的红麻芯材的残留硬度)

摘要

Liquefactions of kenaf core wood were carried out at different phenol-kenaf (P/k) ratios. Characterizations of kenaf core wood liquefied residue were carried out to measure the degree of liquefaction. This provides a new approach to understand some fundamental aspects of the liquefaction reaction. Functional groups on the raw kenaf core wood and liquefied residue were examined using Fourier transform infrared spectroscopy (FTIR). The crystallinity index of the kenaf wood liquefied residue, which represents crystallinity changes of the cellulose component after the liquefaction process, was studied using X-ray diffraction (XRD). The surface morphology of the wood residue was observed using scanning electron microscopy (SEM). The thermal behavior of the residues was analyzed using thermogravimetric analysis (TGA). Abroad peak around 3450-3400 cm-1 representing OH stretching in lignin start to disappear as P/K ratio increases. The results showed that the higher the P/K ratio the greater the liquefaction of the lignin component in the kenaf core wood. The crystallinity index (CrI) on the kenaf liquefied residues increased with the increase in P/K ratio. SEM images showed that the small fragments attached on the liquefied kenaf residue surface were gradually removed as the P/K ratio was increased from 1.5/1.0 to 2.5/1.0, which is mainly attributed to the greater chemical penetration toward reactive site of the kenaf fibres. Residue content decreased as the P/K ratio increased from 1.5/1.0 to 2.5/1.0. TGA results showed the increase of heat resistance in the residue as the P/K ratio was increased
机译:洋麻芯木的液化以不同的酚-洋麻(P / k)比进行。对洋麻芯木液化残渣进行表征以测量液化程度。这提供了一种新的方法来了解液化反应的一些基本方面。使用傅里叶变换红外光谱(FTIR)检查了原始洋麻芯木和液化残渣上的官能团。使用X射线衍射(XRD)研究了洋麻木液化残余物的结晶度指数,该指数表示液化过程后纤维素组分的结晶度变化。使用扫描电子显微镜(SEM)观察木材残余物的表面形态。使用热重分析(TGA)分析残留物的热行为。随着P / K比的增加,代表木质素中OH伸展的3450-3400 cm-1附近的国外峰开始消失。结果表明,P / K比越高,洋麻芯木中木质素组分的液化越大。洋麻液化残渣的结晶度(CrI)随P / K比的增加而增加。 SEM图像显示,随着P / K比从1.5 / 1.0增加到2.5 / 1.0,逐渐除去附着在液化洋麻残渣表面上的小碎片,这主要是由于化学物质对洋麻纤维活性部位的渗透性更大。残渣含量随P / K比从1.5 / 1.0增加到2.5 / 1.0而降低。 TGA结果表明,随着P / K比的增加,残余物中的耐热性增加

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