Search / Korean Journal of Chemical Engineering
Korean Chemical Engineering Research,
Vol.57, No.6, 758-762, 2019
바닷물을 이용한 NaBH4 가수분해에 의한 수소발생
Generation of Hydrogen from Hydrolysis Reaction of NaBH4 Using Sea Water
이동용 고분자전해질 연료전지(PEMFC)의 수소발생용으로써 NaBH4는 많은 장점을 갖고 있다. 해상용으로 PEMFC가 사용될 때 해수를 이용해 NaBH4를 가수분해 하면 경제적이다. 그래서 본 연구에서는 NaBH4가수분해 과정에 증류수대신 해수를 이용해 수소를 발생시켰다. 활성탄 담지 Co-B/C 촉매를 사용해 NaBH4 가수분해 특성에 대해 연구하였다. 해수 사용시 NaBH4농도와 NaOH농도가 증가하면서 수소수율이 감소하였다. 높은 NaBH4와 NaOH농도에서 촉매 표면에 부산물이 부착되어 증류수에 비해 수소수율이 감소했다. NaBH4가수분해 활성화에너지는 증류수와 해수 각각 59.3, 74.4kJ/mol로 해수에서 수소발생속도를 증류수와 같이 높이려면 반응온도를 80 °C이상 상승시켜야 함을 보였다.
Sodium borohydride,NaBH4, has many advantages as hydrogen source for portable proton exchange membrane fuel cells (PEMFC). When PEMFC is used for marine use, NaBH4 hydrolysis using seawater is economical. Therefore, in this study, hydrogen was generated by using seawater instead of distilled water in the process of hydrolysis of NaBH4. Properties of NaBH4 hydrolysis reaction using activated carbon supported Co-B/C catalyst were studied. The yield of hydrogen decreased as NaBH4 concentration and NaOH concentration were increased during NaBH4 hydrolysis using sea water. At higher concentrations of NaBH4 and NaOH, byproducts adhered to the surface of the catalyst after hydrolysis reaction using sea water, reduced hydrogen yield compared to distilled water. The activation energy of NaBH4 hydrolysis is 59.3, 74.4 kJ/mol for distilled water and sea water, respectively. In order to increase the hydrogen generation rate in seawater as high as distilled water, the reaction temperature has to be increased by 80 °C or more.
[References]
  1. Commercial Drones: Highways in the Sky, Worldwide, 2015 to 2021, http//wintergreenresearch.com/reports/Commercial UAS.html.
  2. Bradley TH, Moffitt BA, Mavris DN, Parekh DE, J. Power Sources, 171(2), 793, 2007
  3. Liu BH, Li ZP, J. Power Sources, 187(2), 527, 2009
  4. Fernandes R, Patel N, Miotello A, Jaiswal R, Kothari DC, Int. J. Hydrog. Energy, 36(21), 13379, 2011
  5. Moon GY, Lee SS, Yang GR, Song KH, Korean J. Chem. Eng., 27(2), 474, 2010
  6. Simagina VI, Netskina OV, Komova OV, Odegova GV, Kochubei DI, Ishchenko AV, Kinet. Catal., 49(4), 568, 2008
  7. Simagina VI, Storozhenko PA, Netskina OV, Komova OV, Odegova GV, Samoilenko TY, Gentsler AG, Kinet. Catal., 48(1), 168, 2007
  8. Demirci UB, Garin F, Catal. Commun., 9(6), 1167, 2008
  9. Chen Y, Kim H, Mater. Lett., 62, 1451, 2008
  10. Hwang B, Jo A, Sin S, Choi D, Nam S, Park K, Korean Chem. Eng. Res., 51(1), 35, 2013
  11. Lee HR, Na IC, Park KP, Korean Chem. Eng. Res., 54(5), 587, 2016
  12. Oh SJ, Jung HS, Jeong JJ, Na IC, Ahn HG, Park KP, Korean Chem. Eng. Res., 53(1), 11, 2015
  13. Hwang B, Jo J, Sin S, Choi D, Nam S, Park K, Korean Chem. Eng. Res., 49(5), 516, 2011