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Hydrothermal catalytic gasification of fermentation residues from a biogas plant

机译:沼气厂发酵残留物的水热催化气化

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Biogas plants, increasing in number, produce a stream of fermentation residue with high organic content, providing an energy source which is by now mostly unused. We tested this biomass as a potential feedstock for catalytic gasification in supercritical water (T ≥ 374 ℃, p ≥ 22 MPa) for methane production using a batch reactor system. The coke formation tendency during the heat-up phase was evaluated as well as the cleavage of biomass-bound sulfur with respect to its removal from the process as a salt. We found that sulfur is not sufficiently released from the biomass during heating up to a temperature of 410 ℃. Addition of alkali salts improved the liquefaction of fermentation residues with a low content of minerals, probably by buffering the pH. We found a deactivation of the carbon-supported ruthenium catalyst at low catalyst-to-biomass loadings, which we attribute to sulfur poisoning and fouling in accordance with the composition of the fermentation residue. A temperature of 400 ℃ was found to maximize the methane yield. A residence time dependent biomass to catalyst ratio of 0.45 g g h was found to result in nearly full conversion with the Ru/C catalyst. A Ru/ZrO_2 catalyst, tested under similar conditions, was less active.
机译:沼气厂的数量不断增加,产生的发酵残渣流中有机物含量高,提供了目前几乎未使用的能源。我们使用分批反应器系统测试了该生物质作为超临界水中(T≥374℃,p≥22 MPa)催化气化生产甲烷的潜在原料。评估了加热阶段的焦炭形成趋势,以及结合生物质的硫以盐的形式从工艺中脱除的裂解过程。我们发现,在加热到410℃的温度期间,硫不能从生物质中充分释放出来。碱盐的添加可能通过缓冲pH值来改善具有低矿物质含量的发酵残渣的液化。我们发现了低载量的生物负载碳负载的钌催化剂失活,这归因于硫中毒和结垢,具体取决于发酵残留物的组成。发现温度为400℃可使甲烷产量最大化。发现停留时间依赖性的生物质与催化剂之比为0.45g g·h导致Ru / C催化剂几乎完全转化。在相似条件下测试的Ru / ZrO_2催化剂活性较低。

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