木屑对流干燥与红外干燥扩散系数的比较研究

M. Pryce, D. Cheneler, A. Martín, F. Aiouache
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引用次数: 0

摘要

对流和红外卤素干燥工艺在木屑生物质工业中用于测试木屑的水分含量。木片干燥,虽然能源密集,是必要的,以增加木片的热量含量,反过来增加可燃性。木片生产中的散装过程采用搅拌对流干燥。分析木材中的扩散可以用来估计将木材干燥到指定含水率值所需的时间。温度和水分含量的影响之间的关系允许更准确的预测和干燥器的操作评估。本研究的目的是通过比较在328K、338K、348K和358K热源温度下批量干燥木屑生物质样品时的干燥曲线,来研究恒定热源对流干燥和红外干燥。这是通过比较指数前扩散系数和活化能来实现的,确定了这些术语在湿木材的对流和红外干燥中的温度依赖性。较低的温度增加了对流干燥和红外干燥的干燥时间,其中对流干燥比红外干燥时间长5倍。红外干燥的指前扩散系数和活化能分别为3.555 ×10±0.824 ×10 m2。s-1和3.405 ×10±0.065 ×10 j.l l-1。计算得到的对流干燥指前扩散系数和活化能为2.948 ×10±0.376 ×10 m2。s-1和1.619 ×10±0.037 ×10 j.l l-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comparative Study of Diffusion Coefficients from Convective and IR Drying of Woodchip
Convective and infared (IR) Halogen Drying processes are used in the woodchip biomass industry to test the moisture content of woodchip. Woodchip drying, though energy intensive, is necessary to increase the calorific content of woodchip, in turn increasing combustibility. The bulk process within the production of woodchip uses convective drying with agitation. Analysis of the diffusion in wood can be used to estimate the time to dry lumber to a specified moisture content value. Relationships between the effect of temperature and moisture content allow more accurate predictions and operational evaluations of driers. The aim of this study was to investigate constant heat source convective and IR drying by comparing the drying curves when batch drying a sample of woodchip biomass whilst controlling the heat source temperature at 328K, 338K, 348K and 358K. This was achieved through comparison of preexponential diffusion coefficients and activation energy, determining the temperature dependency of these terms in convective and IR drying of wetted wood. Lower temperatures increased drying time for both convective and IR drying, with convective drying taking up to 5 times longer than IR. The preexponential diffusion coefficient and activation energy found for IR drying were 3.555 ×10±0.824 ×10 m2.s-1 and 3.405 ×10±0.065 ×10 J.mol-1. The convective drying preexponential diffusion coefficient and activation energy calculated was 2.948 ×10±0.376 ×10 m2.s-1 and 1.619 ×10±0.037 ×10 J.mol-1 respectively.
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