Simulation Study for Determining Optimal Operation Window of Iodine Excess for SI Thermochemical Cycle for Hydrogen Production

DOI : 10.17577/IJERTV3IS061127

Download Full-Text PDF Cite this Publication

Text Only Version

Simulation Study for Determining Optimal Operation Window of Iodine Excess for SI Thermochemical Cycle for Hydrogen Production

Dr. Satchidanand R Satpute* Associate Professor, Department of Chemical Engineering, College of Engineering, Bharati Vidyapeeth University, Dhanakwadi, Pune

Dr. Shripad T Revankar Professor of Nuclear Engineering, School of Nuclear Engineering, Purdue University West Lafayette, IN 47907-1290,USA.

Dr. Prakash V Chavan

Professor and Head, Dept. of Chemical Engineering, College of Engineering, Bharati Vidyapeeth University, Dhanakwadi, Pune

Abstract –Energy sustainability issue has driven technology for selecting hydrogen as viable future energy source. The SI(Sulfur iodide) cycle was found to be one of the best cycle for large scale hydrogen production. The Bunsen reaction and phase separation forms important parts of SI thermochemical cycle and were considered for study in the paper. HI/H2SO4/I2/H2O of 2/1/n/12 was used in accordance with recent literature data.

Effect of iodine on reduction of components in HIx phase was studied. The optimal operating range was obtained from the study. Iodine excess of 4-6 was obtained as optimal range for operation whereas water excess was fixed at 12. The optimal range found was 305-320 K.

Keywords: Bunsen reaction, liquid-liquid equilibrium, phase separation, hydrogen production, SI cycle.

INTRODUCTION

from water, in which primary heat input is high temperature from Advanced nuclear reactor. Their evaluation concluded Sulfur-Iodide thermochemical water splitting cycle to be the best, for large scale hydrogen production using high temperature heat from nuclear reactor. A well established sulfur-iodine (SI) process was developed at General Atomics (GA)[1-4]. The SI process consists of three chemical processes, which sum to the dissociation of water as shown in Figure 1. These processes are as follows:

Bunsen reaction (Section I) :

I2(l)+SO2(g)+2H2O(l)2HI(aq)+H2SO4

(aq)(~120°C) (1)

Sulfuric acid decomposition.(Section II): H2SO4(aq) H2O+SO2(g)+½O2(g) (~850oC)

Energy security for the future has driven research to find reliable and sustainable source of energy that is renewable. Hydrogen is found to be promising energy carrier for a sustainable energy system in the future and can be produced

Hydridic acid decomposition (Section III): 2HI(g) H2(g)+I2(g) (~450°C min.)

(2)

(3)

through variety of methods. Numbers of cycles were studied for this purpose. The team of General Atomics (GA), Sandia National Laboratories (SNL) and the University of Kentucky (UK) studied available literature in view of evaluating thermo chemical processes that offer potential for efficient, cost effective, large scale production of hydrogen

Net reaction: H2O H2 + ½O2 (4)

For Section I (Bunsen Process), GA modified the earlier flowsheet [3], since the previous thermodynamic model was insufficient to perform a strictly thermodynamic model. This restricted their ability to fully optimize the flowsheet. The earlier flowsheet for Section I was modified by changing the flow rates to match the modified versions of Sections II and III.. As explained in section 2[3], there are several issues with Bunsen reaction and hence improvements are being considered. Here in this work the effect of iodine is studied for Bunsen reaction and phase separation section in SI cycle.

Figure 1: SI thermochemical cycle schematic

  1. ISSUES WITH BUNSEN REACTION

    Section I Bunsen reaction, is exothermic and it is carried out in liquid phase at 120 0C. In this reaction, water reacts with I2 and SO2 to produces H2SO4 and HI, in two immiscible aqueous phases. Bunsen process, is typically operated in liquid water media with a large excess of iodine to avoid side processes between iodine and sulfur compounds, and to segregate the two product acids into two corresponding liquid phases: a sulfuric acid phase(SA phase) in which HI exhibits low solubility, and a hydrogen iodide phase (HIx phase)

    containing almost all of the excess iodine and in which H2SO4 is only slightly soluble. Hence, the reaction stoichiometry and mass balance of this process can be described as follows:

    (1+x)I2 + SO2 +(2+n)H2O H2SO4 +(n-m)H2O|Sulfuric acid phase + [2HI +I2 + mH2O]HIx phase

    (5)

    where x and n are the iodine and water molar excess quantities, respectively, and m is the molar quantity of the excess water, n, that ends up in the HIx phase. Although the excess water in the Bunsen process helps to make this process thermodynamically favorable, the exothermic processes at low temperature and the high irreversibility due to the large negative change in the Gibbs free energy

    lead to a significant energy loss, because the heat released at low temperature cannot be effectively recovered, and the irreversible process reduces the cycle efficiency.

    Other alternative methods to segregate the acids have been recently suggested in the Bunsen process. These include (i) adjustment of the process solvent to segregate the acid products by the use of a solvent other than water,

    (ii) a novel route involving the addition of a precipitating agent to separate iodide from sulfate by means of solid salt formation by ion exchange processes, and (ii) carrying out the Bunsen process in an electrochemical cell with membranes [14].

  2. SIMULATION METHODOLOGY

    In present work, simulation of Bunsen reaction and separator in SI cycle were investigated. The study was aimed at studying the effect of iodine in feed on phase separation i.e HIx phase and SA phase. Figure 2 shows the ASPEN model used for liquid-liquid separation. Thermodynamic model used was ELECNRTL. I2/HI mixture from step 1 was mixed with sulfuric acid at room temperature. Residual water with was added to separator. Two phase separation (SA phase and HIx phase occurs in decanter(SEP2). The temperature range used was 290- 400K. water excess used was 12 mole excess whereas it was based on H2SO4 moles. The iodine excess was varied from 1 to 12 mole excess. So feed composition chosen were HI/H2SO4/I2/H2O=2/1/n/12, where n varied from 1- 12.

    SAPHASE

    STEP1

    HI

    TCON1

    STEP2

    TCON2

    HI-I2 I2HI

    I2 MIXTURE

    RTEMPMIX

    2-SEP

    H2SO4

    RH2O

    HIX

    Figure 2: Model for Bunsen reaction with separation

  3. RESULT AND DISCUSSION

    0.15

    4

    0.2

    5

    0.25

    I2 H2O

    H2SO4

    6

    Mol ratio to HI in Hix phase

    H2SO4/HI in Hix phase

    Last decade many researcher [5-15] have studied Bunsen reaction and phase separation experimentally that forms the important part of SI thermo chemical cycle. The effect of Iodine and water excess on Bunsen reaction and

    phase separation were studied. The contaminations in Sulfuric acid (SA)phase and Hydriodic acid(HA) phase were observed to reduce with increase of iodine concentration in feed. Present work study the effect of iodine on phase separation.

    7

    0.3

    0

    0

    0 2 4

    6

    I2/H2SO4 in feed

    8

    10

    12

    0.05

    1

    0.1

    3

    2

    Figure 3: Effect of Iodine on component in HIx phase

      1. Contamination/distribution of components in phases.

        HIx is more important than SA phase being directly involved in hydrogen production. Figure 3 depict the effect of iodine excess in feed on components in HIx phase. H2SO4 contamination in HIx phase was observed to reduce drastically as iodine improves fro 1 to 4 and

        then reduce marginally after 4. The H2O concentration was also observed to diminish as iodine improves 1-4 and then very gradual decreases. The iodine prefers HIx phase compared to SA phase and hence there is corresponding increase in concentration of iodine in HIx phase with improvement in iodine in feed. This observation coincides with observation with experimental data [6-13].

        Figure 5: Optimal range study

      2. Optimal range

    The optimal range study is demonstrated in Figure 5. The effect of temperature and iodine excess in feed was studied simultaneously to find out the optimal range of operation. Iodine excess of 4-6 could be concluded as optimal range as minimum contamination points corresponds to that reason and temperature range of 305- 320K corresponds to minimum contamination zone.

  4. CONCLUSION

Simulation was performed to study the Bunsen reaction and phase separation. Effect of iodine excess in feed on phase separation i.e. reduction of contamination in HIx phase was studied successfully. Simulation results also

matches same trend of reduction as in literature experimental data and has predicted the optimal iodine range.

REFERENCE

  1. Brown L.C., Besenbruch G.E., Lentsch R.D., Schultz K.R., Funk J.F., Pickard P.S., Marshall A.C., and Showalter S.K. High efficiency generation of hydrogen fuels using nuclear powerfinal technical report for the Period August 1, 1999 through September 30, 2002, Prepared under the Nuclear Energy Research Initiative (NERI) Program grant no. DE- FG03-99SF21888 for the US Department of Energy, June, 2003.

  2. Revankar S. T. and Oh S., 2005, Simulation of sulfur iodine thermochemical water splitting process using ASPEN PLUS, Purdue University School of Nuclear Engineering Report, July, PU/NE-05-06, 2005.

  3. Norman J.H., Besenbruch G.E, OKeefe D.R. and Allen C.L. Thermochemical Water-Splitting Cycle, Bench-Scale Investigations, and Process Engineering, Final Report for the Period February 1977 through December 31, 1981, General Atomics Report GAA16713, DOE Report DOE/ET/26225- 1, 1981.

  4. Zhu Qiaoqiao, Zhang Yanwei, Zhou Chao, Wang Zhihua, Zhou Junhu, Gen Kefa. Optimisation of liquid-liquid phase separation characteristics in the Bunsen section of the sulfur- iodinehydrogen production process,Int J of Hydrogen energy, 2012, 37(8), 64076414

  5. Lee BJ, No HC, Yoon HJ, Kim SJ, Kim ES. An optimal operating window for the Bunsen process in the SI thermochemical cycle. Int J Hydrogen Energy 2008l 33(9): 2200-2210.

  6. Giaconia A, Caputo G, Ceroli A, Diamanti M, Barbarossa V, Tarquini P, Sau S. Experimental study of two phase separation in the Bunsen section of the sulfur-iodine thermochemical cycle. Int. J of Hydrogen Energy 2007; 32: 531-536.

  7. Norman JH, Besenbruch GE, Brown LC. Thermochemical water splitting cycle. Bench-scale investigatios and process engineering. DOE/ET/26225,1981.

  8. Colette S, Brijou-Mokrani N, Carles P, Fauvet P, Tabarant M, Dutruc-Rosset C. Experimental study of Bunsen reaction in the framework of massive hydrogen production by the sulfur-iodide thrmochemical cycle. WHEC 16/13-16 June 2006, Lyon, France.

  9. Sakurai M, Nakajima H, Onuki K, Ikenoya K, Shimizu S. Preliminary process analysis for the closed cycle operation of the Iodine-sulfur thermochemical hydrogen production process. Int J. of Hydrogen energy 1999;24:603-612.

  10. Sakurai M, Nakajima H, Onuki K, Shimizu. Investigation of 2 liquid phase separation characteristics on the iodine- sulfur thermochemical hydrogen production process. Int. J. of Hydrogen energy 2000; 25: 605-611.

  11. Sakurai M, Nakajima H, Amir R, Onuki K, Shimizu S. Experimental study on side-reaction occurrence condition in the iodine-sulfur thermochemical hydrogen production process. Int J. of Hydrogen Energy 2000;25:613-9.

  12. Lee TC, Jeong HD, Kim TH, Bae GG. The study on 2 liquid separation characteristics of H2SO4-HI-H2O-I2 System (I). J. Korean Ind. Eng. Chem 2005; 16 (6): 848-852.

  13. Kang YH, Ryu JC, Park CS, Hwang GJ, Lee SH, Bae Kk. The study on the Bunsen reaction process for iodine-sulfure thermochemical hydrogen production. Korean Chem. Eng Res 2006;44(4):410-416

  14. Kubo S, Nakajima H, Kasahara S, Higashi S, Masaki T, Abe H et.al. A demonstration study on a closed-cycle hydrogen production by the thermochemical water-splitting iodine sulfur process. Nucl. Eng Des 2004;233:347-54.

  15. Giaconia Alberto, Caputo Giampaolo, Tarquini Pietro, Sau Salvatore, Prosini Pier Paolo, Pozio Alfonso, Nardi Luigi. Survey of Bunsen reaction routes to improve the sulfur-iodine thermochemical water-splitting cycle. Int. J. of Hydrogen Energy 2009;34:4041-4048.

Leave a Reply