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《高校化学工程学报》2021,35(2)
生物质基平台化合物糠醛和5-羟甲基糠醛来源广泛,可从绿色植物中提取得到。糠醛和5-羟甲基糠醛双键加氢制备四氢糠醇和2,5-二羟甲基四氢呋喃具有重要的研究价值。文章综述了近年来糠醛和5-羟甲基糠醛双键加氢反应的研究成果,重点阐述了反应机理的研究进展,讨论了不同催化体系(单金属、合金)对糠醛和5-羟甲基糠醛双键加氢的催化作用,并对后续催化剂的研究方向和应用前景作了展望。 相似文献
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通过生物质衍生糖的酸催化转化制备生物质基平台化合物5-羟甲基糠醛受到关注。常用又有效的溶剂包括离子液体和二甲基亚砜等,但这些溶剂黏度高,易造成空气污染。以γ-戊内酯作为溶剂,研究果糖催化转化为5-羟甲基糠醛的绿色过程,系统研究酸催化剂种类、反应温度、催化剂用量、果糖初始浓度及底物种类等对5-羟甲基糠醛产率的影响。通过反应条件的优化,以HCl溶液为催化剂,在果糖初始质量浓度2%、反应温度100℃和反应时间30 min条件下,5-羟甲基糠醛产率为93.5%。5-羟甲基糠醛产率随果糖初始添加量的增加而呈下降趋势,但果糖初始质量浓度为10%时,5-羟甲基糠醛产率仍保持约90%,表明γ-戊内酯是一种将果糖催化转化为5-羟甲基糠醛的优良绿色溶剂。 相似文献
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SO_4~(2-)/ZrO_2固体超强酸催化剂金属离子复合、改性及在乙酰丙酸制备中的研究 总被引:1,自引:0,他引:1
采用共沉淀法制备了SO42-/ZrO2-Fe2O3和SO42-/ZrO2-Al2O3双金属固体超强酸催化剂,其中SO42-/ZrO2-Fe2O3对葡萄糖水解生成5-羟甲基糠醛的反应有利,而SO42-/ZrO2-Al2O3对5-羟甲基糠醛脱羧生成乙酰丙酸的反应有利。采用沉淀-浸渍法制取两种金属离子改性的SO42-/ZrO2催化剂,该类催化剂对葡萄糖水解制5-羟甲基糠醛和5-羟甲基糠醛脱羧生成乙酰丙酸的反应均有利。 相似文献
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D. G. Gordeev L. F. Gudarenko M. V. Zhernokletov V. G. Kudel’kin M. A. Mochalov 《Combustion, Explosion, and Shock Waves》2008,44(2):177-189
A semi-empirical equation of state for metals is described. Its capabilities are demonstrated by the example of the equation
of state for aluminum. New experimental data are presented on the location of the isentrope of aluminum for unloading from
the state at p = 229.71 GPa on the shock adiabat to an aerogel (SiO2) of density 0.08 g/cm3.
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Translated from Fizika Goreniya i Vzryva, Vol. 44, No. 2, pp. 61–75, March–April, 2008. 相似文献
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The objective of the study was to explore the effect of the degree of deacetylation (DD) of the chitosan used on the degradation rate and rate constant during ultrasonic degradation. Chitin was extracted from red shrimp process waste. Four different DD chitosans were prepared from chitin by alkali deacetylation. Those chitosans were degraded by ultrasonic radiation to different molecular weights. Changes of the molecular weight were determined by light scattering, and data of molecular weight changes were used to calculate the degradation rate and rate constant. The results were as follows: The molecular weight of chitosans decreased with an increasing ultrasonication time. The curves of the molecular weight versus the ultrasonication time were broken at 1‐h treatment. The degradation rate and rate constant of sonolysis decreased with an increasing ultrasonication time. This may be because the chances of being attacked by the cavitation energy increased with an increasing molecular weight species and may be because smaller molecular weight species have shorter relaxation times and, thus, can alleviate the sonication stress easier. However, the degradation rate and rate constant of sonolysis increased with an increasing DD of the chitosan used. This may be because the flexibilitier molecules of higher DD chitosans are more susceptible to the shear force of elongation flow generated by the cavitation field or due to the bond energy difference of acetamido and β‐1,4‐glucoside linkage or hydrogen bonds. Breakage of the β‐1,4‐glucoside linkage will result in lower molecular weight and an increasing reaction rate and rate constant. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3526–3531, 2003 相似文献
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Jorge Marcelo Romero Soledad Bustillo Hugo Enrique Ramirez Maisuls Nelly Lidia Jorge Manuel Eduardo Gómez Vara Eduardo Alberto Castro Alicia H. Jubert 《International journal of molecular sciences》2007,8(7):688-694
A thermochemical rather simple experimental technique is applied to determine the enthalpy of formation of Diperoxide of ciclohexanone. The study is complemented with suitable theoretical calculations at the semiempirical and ab initio levels. A particular satisfactory agreement between both ways is found for the ab initio calculation at the 6–311G basis This set level. Some possible extensions of the present procedure are pointed out. 相似文献
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醋酸纤维素取代基分布与性质的关系 总被引:9,自引:0,他引:9
分析了以吡啶为溶剂的醋酸纤维素的13C-NMR核磁共振谱,得出了三种不同位置羟基的取代度。结合X—射线和DSC分析,初步说明具有相同取代度但未经水解和经过水解的醋酸纤维素(CA) 性质上的差异是由于三个羟基上的取代度分布不同及消晶程度差异所致。 相似文献
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介绍了平板硫化机热板中高度在硫化排气过程中的作用及其实现途径和评价方法;提出了设置热板中高度时应遵守的"刚性横梁、柔性热板"概念和"最短路径、最小排气阻力"原则;探讨了横梁热变形对热板中高度的影响。结果表明,参考横梁热变形设置的热板中高度有助于解决平板硫化机在复杂状态下硫化制品时的表面排气问题。 相似文献
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A Review of Contemporary Views of Theories of Adhesion 总被引:2,自引:0,他引:2
K. W. Allen 《The Journal of Adhesion》1987,21(3):261-277
The once distinct and independent theories of adhesion have been losing their isolation and converging. Ideas of the effects of surface roughness, once dismissed as irrelevant except in the case of textiles, have been revised; albeit on a smaller scale as details of surfaces have been revealed by sophisticated techniques. Electrostatic interactions across an interface have been more deeply explored and their significance recognised and expounded. Diffusion of groupings and chain segments within a polymer have been related to the possibilities of interaction with a variety of surfaces. Perhaps most important, theories of adsorption have been extended in depth. The precise nature of the molecular interactions have been recognised and quantified. In doing this the contribution of diffusion and elastoplastic phenomena have been integrated. These developments are collated and analysed to present the present understanding of the concepts. 相似文献