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bio-FLASHCHAIN® theory for rapid devolatilization of biomass 1. Lignin devolatilization

机译:bio-FLASHCHAIN®理论,用于生物质的快速脱挥发分1.木质素脱挥发分

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摘要

This study validates a modeling framework to accurately predict the total and tar yields from any lignin at any devolatilization conditions. The original reaction mechanism and depolymerization kinetics in bio-FLASHCHAIN (R) are slightly modified for pure lignin, and used to accurately interpret how the molecular weight distribution (MWD) of a lignin governs its primary devolatilization behavior. The only sample-specific input requirements are an ultimate analysis and a weight-average molecular weight (M-W), although a measured M-W-value is not needed for lignin in whole biomass. Predicted total and tar yields are validated with measured values from 20 diverse lignins for heating rates from 10 degrees C/min to 5000 degrees C/s to temperatures from 430 to 950 degrees C with contact times of several seconds. Predicted tar yields increase for progressively lighter lignin MWDs, and accurately depict how variations in lignin MWD affect total volatiles yields. The strong impact of lignin MWD on its primary devolatilization behavior is accurately interpreted by the flash distillation analogy without any adjustments to the reaction kinetics for a diverse assortment of lignins. The entire reaction mechanism in bio-FLASHCHAIN (R) is required with non-pyrolytic lignins, whose predicted total and tar yields increase in inverse proportion to reductions in M-W. For pyrolytic lignins, bridge scission is superfluous because the whole lignin falls within the size range for tar precursors initially and throughout devolatilization. Consequently, neither total nor tar yields are affected by M-W variations because the tar vaporization rates are maximized throughout this M-W range. Devolatilization shifts toward hotter temperatures for progressively faster heating rates, in good agreement with data, whereas predicted total and tar yields are insensitive to heating rate variations. Total yields increase for progressively hotter temperatures due to the transition from tar production to char decomposition in the reaction mechanism. Tar yields saturate to an asymptotic ultimate value at approximately 550 degrees C for fast heating rates.
机译:这项研究验证了一个建模框架,可以准确预测在任何脱挥发分条件下任何木质素的总产率和焦油产率。对于纯木质素,bio-FLASHCHAIN(R)中的原始反应机理和解聚动力学进行了轻微修改,并用于准确解释木质素的分子量分布(MWD)如何控制其主要的脱挥发分行为。样品特定输入的唯一要求是最终分析和重均分子量(M-W),尽管木质素在整个生物质中不需要测量的M-W值。预测的总收率和焦油收率由20种不同木质素的测量值验证,加热速率从10摄氏度/分钟到5000摄氏度/秒,到温度从430到950摄氏度,接触时间为几秒钟。逐渐变轻的木质素MWD的预计焦油收率会增加,并准确描述木质素MWD的变化如何影响总挥发物的收率。闪蒸类比法可以准确地解释木质素MWD对其主要脱挥发分行为的强烈影响,而无需对多种木质素的反应动力学进行任何调整。非热解木质素需要bio-FLASHCHAIN(R)中的整个反应机理,其预测的总产率和焦油产率与M-W的降低成反比。对于热解木质素,不需要进行桥断裂,因为整个木质素在最初和整个脱挥发分时都在焦油前体的尺寸范围内。因此,总焦油产率和焦油产率都不受M-W变化的影响,因为在整个M-W范围内,焦油蒸发速率都达到了最大值。与数据完全吻合,脱挥发分会朝着更高的温度转变,以逐渐提高加热速率,而预测的总产率和焦油产率对加热速率的变化不敏感。由于在反应机理中从焦油生成到焦炭分解的过渡,温度逐渐升高时总收率增加。对于快速加热速率,焦油产率在大约550摄氏度时饱和至渐近极限值。

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