A facile synthesis route to improve the catalytic activity of inherently cationic and magnetic catalyst systems for hydrogen generation from sodium borohydride hydrolysis


ŞAHİNER N., Seven F.

FUEL PROCESSING TECHNOLOGY, cilt.132, ss.1-8, 2015 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 132
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1016/j.fuproc.2014.12.008
  • Dergi Adı: FUEL PROCESSING TECHNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1-8
  • Çanakkale Onsekiz Mart Üniversitesi Adresli: Evet

Özet

Inherently cationic poly(3-acrylamidoproply)trimethylammonium chloride) (p(APTMACl)) as hydrogel and cryogel as nonporous and superporous structures to use as template for cobalt and Nickel metal nanoparticle preparation and then H-2 production from NaBH4 hydrolysis. Use of p(APTMACl) hydrogels in H-2 generation reactions from hydrolysis is an advantage due to their inherently cationic nature and no requirement for any modification/quaternization steps to load metal salts for in situ metal nanoparticle preparation. However, it is very well known that the metal loading processes of p(APTMACl) hydrogels are very slow. Therefore, the superporous cryogels prepared from p(APTMACl) offered great advantages in terms of swelling, metal absorption for in situ metal nanoparticle preparation, and then higher catalytic activity in hydrolysis of NaBH4. The p(APTMACl) cryogels and their metal composites provide 32, 3600, 1.5, 5.5 and 3.5 fold faster swelling degree, swelling time, metal absorption capacity, metal absorption time and H-2 generation rate, respectively than hydrogels and metal composites. In addition, p(APTMACl)-Co metal composites are shown to have highly useful characteristics in H-2 generation reaction from hydrolysis of NaBH4, due to their innate magnetic character, which allows control by an externally applied magnetic field, and reusability, with almost 80% at the end of 5th use. (C) 2014 Elsevier B.V. All rights reserved.