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生物质基催化剂在CO_(2)化学转化中的应用
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作者 高晋彬 陆颖琪 +2 位作者 张辉 高利柱 熊兴泉 《有机化学》 SCIE CAS CSCD 北大核心 2024年第9期2732-2741,共10页
CO_(2)是地球上储量最丰富的C1资源,其特点是无毒、可再生、化学性质稳定和价廉易得.因此,通过化学转化方法将CO_(2)转化为具有高附加值的化学品有着重要的意义.由于CO_(2)具有较高的热力学稳定性和动力学惰性,导致基于它的大部分化学... CO_(2)是地球上储量最丰富的C1资源,其特点是无毒、可再生、化学性质稳定和价廉易得.因此,通过化学转化方法将CO_(2)转化为具有高附加值的化学品有着重要的意义.由于CO_(2)具有较高的热力学稳定性和动力学惰性,导致基于它的大部分化学转化反应都需要使用高效催化剂.迄今为止,多孔碳、离子液体(ILs)、共价有机框架(COFs)、多孔有机聚合物(POPs)和金属有机框架(MOFs)等均已被用于CO_(2)的化学转化,这些催化体系虽然具有较高的催化活性,但也存在诸多缺点,如原料来源较为困难且这些原料大多不可再生,制备过程不绿色或制备成本昂贵.因此,发展天然小分子或天然高分子为原料制备可再生生物质基催化剂显得尤为重要.综述了含有天然产物的催化体系,如氨基酸、胆碱、纤维素、壳聚糖和木质素等在以CO_(2)制备高附加值化学品方面的研究进展. 展开更多
关键词 生物质基催化剂 CO_(2) 化学转化 绿色合成
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生物质基固体酸催化剂的制备及其催化糖转化性能的研究
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作者 黄婷 周姚红 +2 位作者 章黄娴 袁坤 熊万明 《精细化工中间体》 CAS 2021年第5期64-69,共6页
采用松果壳、花生壳、核桃壳及玉米秸秆等自然生物质为原料,通过不完全碳化-浓硫酸磺化两步制备生物质基固体酸催化剂,并将其用于油浴加热及微波条件下催化单糖转化为呋喃平台化合物实验中,两种加热方式下(150℃油浴8 h,160℃微波辅助10... 采用松果壳、花生壳、核桃壳及玉米秸秆等自然生物质为原料,通过不完全碳化-浓硫酸磺化两步制备生物质基固体酸催化剂,并将其用于油浴加热及微波条件下催化单糖转化为呋喃平台化合物实验中,两种加热方式下(150℃油浴8 h,160℃微波辅助10 min),获得的糠醛及5-羟甲基糠醛的收率作为其催化性能的评价指标。果糖转化实验中显示四种催化剂获得5-羟甲基糠醛的能力无明显差异,5-羟甲基糠醛收率均在70%左右。催化木糖及葡萄糖的活性均表现为核桃壳SC>松果壳SC>玉米秸秆SC>花生壳SC,其中核桃壳SC催化木糖制备糠醛收率可达55.38%,催化葡萄糖制备5-羟甲基糠醛收率可达23.31%。 展开更多
关键词 生物质固体酸催化剂 木糖 果糖 葡萄糖 糠醛 5-羟甲糠醛
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生物质基磁性固体酸催化玉米秸秆液化工艺的研究 被引量:1
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作者 李学琴 王志伟 +4 位作者 李翔宇 杨淼 徐海燕 何晓峰 雷廷宙 《河南科学》 2019年第4期545-551,共7页
通过热化学液化法,以乙二醇、聚乙二醇、丙三醇的混合比例、催化剂种类、催化剂量、液化温度、液化时间为影响因素,液化率为指标,采用单因素试验和正交试验优化生物质基磁性固体酸催化玉米秸秆多组分溶剂液化工艺条件.利用最佳工艺条件... 通过热化学液化法,以乙二醇、聚乙二醇、丙三醇的混合比例、催化剂种类、催化剂量、液化温度、液化时间为影响因素,液化率为指标,采用单因素试验和正交试验优化生物质基磁性固体酸催化玉米秸秆多组分溶剂液化工艺条件.利用最佳工艺条件下制备的玉米秸秆液化油替代多元醇制备聚氨酯发泡材料,对发泡体进行观察.结果表明,7个因素对玉米秸秆液化率影响的主次顺序为乙二醇量>聚乙二醇量>液化温度>液化时间>催化剂种类>丙三醇量>催化剂量,即最佳工艺条件为液化剂V(乙二醇)∶V(聚乙二醇)∶V(丙三醇)为1∶1.5∶1.5.在玉米秸秆基磁性固体酸作为催化剂,催化剂量为12 g,液化温度135℃,液化时间70 min的条件下,液化玉米秸秆得到最高液化率为72.3%;玉米秸秆液化油替代多元醇能够制备均匀的聚氨酯发泡材料. 展开更多
关键词 生物质磁性固体酸催化剂 玉米秸秆 多组分溶剂 液化
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生物质碳基固体酸催化剂的制备及其对酯化反应的催化性能 被引量:7
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作者 刘晓红 付小琴 代超 《环境工程学报》 CAS CSCD 北大核心 2019年第10期2530-2536,共7页
为了寻找一种以生物质为原料,能够温和地合成磁性碳基固体酸催化剂的路径,以生物质柚子果皮为原料合成磁性固体酸催化剂,并将其用于催化油酸和乙醇的酯化反应中。结果表明:MPC-0.4-SO3H和MPC-0.8-SO3H在反应温度为80℃、催化剂用量为油... 为了寻找一种以生物质为原料,能够温和地合成磁性碳基固体酸催化剂的路径,以生物质柚子果皮为原料合成磁性固体酸催化剂,并将其用于催化油酸和乙醇的酯化反应中。结果表明:MPC-0.4-SO3H和MPC-0.8-SO3H在反应温度为80℃、催化剂用量为油酸质量的7%、油醇比为1∶20、反应时间为8 h时,酯化率可达到68.0%和68.8%,高于商用催化剂Amberlyst-15的酯化率;2种催化剂耐水性好,稳定性高,重复使用3次和4次时,酯化率仍高于或接近Amberlyst-15。通过分析可知,2种固体酸活化能较低,与Amberlyst-15相比,其催化反应的速率常数更大,在生物柴油的合成中具有较好的应用前景。 展开更多
关键词 生物质固体酸催化剂 酯化反应 催化活性
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Production of Mixed Alcohols from Bio-syngas over Mo-based Catalyst
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作者 仇松柏 黄伟伟 +2 位作者 徐勇 刘璐 李全新 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2011年第1期77-84,I0004,共9页
A series of Mo-based catalysts prepared by sol-gel method using citric acid as complexant were successfully applied in the high efficient production of mixed alcohols from bio-syngas, derived from the biomass gasifica... A series of Mo-based catalysts prepared by sol-gel method using citric acid as complexant were successfully applied in the high efficient production of mixed alcohols from bio-syngas, derived from the biomass gasification. The Cu1Co1Fe1MO1Zn0.5-6%K catalyst exhibited a higher activity on the space-time yield of mixed alcohols, compared with the other Mobased catalysts. The carbon conversion significantly increases with rising temperature below 340 ℃, but the alcohol selectivity has an opposite trend. The maximum mixed alcohols yield derived from biomass gasification is 494.8 g/(kg catal·h) with the C2+ (C2-C6 higher alcohols) alcohols of 80.4% under the tested conditions. The alcohol distributions are consistent with the Schulz-Flory plots, except methanol. In the alcohols products, the C2+ alcohols (higher alcohols) dominate with a weight ratio of 70%-85%. The Mo-based cata- lysts have been characterized by X-ray diffraction and N2 adsorption/desorption. The clean bio-fules of mixed alcohols derived from bio-syngas with higher octane values could be used as transportation fuels or petrol additives. 展开更多
关键词 Biomass Bio-syngas Mixed alcohol Mo-based catalyst Biomass Bio-syngas Mixed alcohol Mo-based catalyst
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Experiments on Ni/γ-Al_2O_3 catalyst for improving lower heating value of biomass gasification fuel gas via methanation 被引量:3
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作者 Dong Xinxin Jin Baosheng +1 位作者 Wang Yanyan Niu Miaomiao 《Journal of Southeast University(English Edition)》 EI CAS 2017年第4期448-456,共9页
Ni-based catalysts supported by γ-Al_2O_3 were prepared for improving the lower heating value( LHV) of biomass gasification fuel gas through methanation. Prior to the performance tests, the physico-chemical propertie... Ni-based catalysts supported by γ-Al_2O_3 were prepared for improving the lower heating value( LHV) of biomass gasification fuel gas through methanation. Prior to the performance tests, the physico-chemical properties of the catalyst samples were characterized by N_2 isothermal adsorption/desorption, X-ray diffraction( XRD) and a scanning electron microscope( SEM). Afterwards, a series of experiments were carried out to investigate the catalytic performance and the results showthat catalysts with 15% and20% Ni loadings have better methanation catalytic effect than those with 5% and 10% Ni loadings in terms of elevating the LHV of biomass gasification fuel gas. M oreover, controllable influential factors such as the reaction temperature, the H_2/CO ratio and the water content occupy an important position in the methanation of biomass gasification fuel gas. 15 Ni/γ-Al_2O_3 and 20 Ni/γ-Al_2O_3 catalysts have a higher CO conversion and CH_4 selectivity at 350 ℃ and the LHV of biomass gasification fuel gas can be largely increased by 34. 3 % at 350 ℃. Higher H_2/CO ratio and a lower water content are more beneficial for improving the LHV of biomass gasification fuel gas when considering the combination of both CO conversion and CH_4 selectivity. This is due to the fact that a higher H_2/CO ratio and lower water content can increase the extent of the methanation reaction. 展开更多
关键词 N i-based catalyst METHANATION BIOMASS gasification fuel gas low er heating value
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Production of succinic acid in basket and mobile bed bioreactors-Comparative analysis of substrate mass transfer aspects
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作者 Anca-Irina Galaction Dan Cascaval +1 位作者 Ramona-Mihaela Matran Alexandra Tucaliuc 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2016年第4期513-520,共8页
The glucose mass transfer in the biosynthesis of succinic acid with immobilized Actinobacillus succinogenes cells has been comparatively analyzed for a bioreactor with mobile bed vs. a stationary basket bioreactor. Th... The glucose mass transfer in the biosynthesis of succinic acid with immobilized Actinobacillus succinogenes cells has been comparatively analyzed for a bioreactor with mobile bed vs. a stationary basket bioreactor. The process has been considered to occur under substrate and product inhibitory effects. The results indicated that the bioreactor with mobile bed is more efficient for biocatalyst particles with a diameter over 3 mm, while the basket bioreactor is more efficient for smaller biocatalyst particles and basket bed thickness below 5 mm. The performances of both configurations of immobilized A. succinogenes cell beds were found to be superior to the column packed bed bioreactor. 展开更多
关键词 Mass transferDiffusionStirred vesselImmobilized cellsBasket bioreactorSuccinic acid
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