دانلود رایگان مقاله اثر اسیدهای جامد زئولیت در محل هیدروژناسیون فنل - زیستی مشتق شده

عنوان فارسی
اثر اسیدهای جامد زئولیت در محل هیدروژناسیون فنل - زیستی مشتق شده
عنوان انگلیسی
Effect of zeolite solid acids on the in situ hydrogenation of bio-derived phenol
صفحات مقاله فارسی
0
صفحات مقاله انگلیسی
6
سال انتشار
2016
نشریه
الزویر - Elsevier
فرمت مقاله انگلیسی
PDF
کد محصول
E2867
رشته های مرتبط با این مقاله
شیمی
گرایش های مرتبط با این مقاله
شیمی کاتالیست، شیمی کاربردی
مجله
ارتباطات کاتالیست - Catalysis Communications
دانشگاه
آزمایشگاه های کلیدی برای فناوری های سبز شیمیایی، مرکز نوآوری های مشترک علم شیمی و مهندسی (تیانجین)، دانشکده مهندسی شیمی و صنعت، دانشگاه تیانجین، چین
کلمات کلیدی
فنل، زیستی نفت، در هیدروژناسیون درجا، رینی نیکل، اسید جامد هر نوع سیلیکات ابدار
چکیده

Abstract


The effect of zeolite solid acids on the in situ hydrogenation of bio-derived phenol over Raney Ni was investigated, which indicated that the conversion of phenol increased with the addition of zeolite solid acids and Hbeta (Si/Al = 60) showed the best performance of high phenol conversion and selectivity towards the desired products and low carbon loss. In addition, the quantity of Hbeta (Si/Al = 60) and Raney Ni had marked impact on the carbon loss, but little effect on both the conversion and the products distribution. And the mixed catalysts of Raney Ni and Hbeta (Si/Al = 60) exhibited excellent stability.

نتیجه گیری

4. Conclusion


In this work, the in situ hydrogenation of phenol to stable oxygenated organics was conducted over Raney Ni and zeolite solid acids. The effect of zeolite solid acids was discussed and the catalytic activities were compared. The conversion of phenol increased with the addition of zeolite solid acids, which indicated that zeolite solid acids could enhance the catalytic activity. And in these tested zeolite solid acids, Hbeta (Si/ Al = 60) was much better than others for in situ hydrogenation of phenol with lower carbon loss and higher conversion and selectivity to the desired products. The main reaction pathway was hydrogenated for benzene ring of phenol to produce cyclohexanone and cyclohexanol. In addition, the quantity of Hbeta (Si/Al = 60) and Raney Ni had marked impact on the carbon loss, but little effect on both the conversion and the products distribution. And the mixed catalysts of Raney Ni and Hbeta (60) exhibited excellent stability after cyclic uses.


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