کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4756756 1419158 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Catalytic ethanolysis of Kraft lignin to small-molecular liquid products over an alumina supported molybdenum nitride catalyst
ترجمه فارسی عنوان
اتانول کاتالیستی کربن لیگنین به محصولات مایع مولکولی کوچک بر روی آلومینا کاتالیست نیوبید مولیبدن
کلمات کلیدی
لیگنین کرافت، اتانولز کاتالیستی، اتانول فوق بحرانی، محصولات کوچک مولکولی، نیترید مولیبدن،
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
چکیده انگلیسی


- An alumina supported molybdenum nitride catalyst for lignin ethanolysis.
- The products are alcohols, esters, mono-phenols, benzyl alcohols and arenes.
- The preparation and reaction conditions have great influences on the activity.
- 907 mg/g lignin aliphatics and 282 mg/g lignin aromatics are obtained.
- No significant activity loss is observed in three runs.

An alumina supported molybdenum nitride catalyst (Mo2N/Al2O3) is examined for the ethanolysis of Kraft lignin in supercritical ethanol in a batch reactor with an initial nitrogen pressure of 0 MPa (gauge). No char or tar is formed in this process. The Mo loading as well as the nitriding temperature in the catalyst preparation process has a great influence on the activity. The best performance is obtained over 30 wt% Mo2N/Al2O3 catalyst nitrided at 700 °C. The overall yields of sulfur-free small-molecular products achieve the maximum value of 1189 mg/g lignin, with aliphatic compounds accounting for 907 mg/g lignin and aromatic compounds 282 mg/g lignin, respectively. Both the product yields and the molecular distribution are also strongly dependent on the reaction time and temperature. Furthermore, the Mo2N/Al2O3 catalyst exhibits an excellent recycle performance with no significant activity loss after at least three runs. After reaction, the bulk structure of Mo2N/Al2O3 catalyst was well-preserved only with a slight surface oxidation.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Catalysis Today - Volume 298, 1 December 2017, Pages 9-15
نویسندگان
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