(328d) Further Development of the Hydrolysis Reactors in the Cu-Cl Cycle | AIChE

(328d) Further Development of the Hydrolysis Reactors in the Cu-Cl Cycle

Authors 

Lewis, M. - Presenter, Argonne National Laboratory
Tatterson, D. - Presenter, Orion Consulting Co

Abstract

Over 200
thermochemical cycles have been identified to produce hydrogen by thermochemical
water decomposition [1]. The Cu-Cl cycle was first proposed by the Institute of
Gas Technology (IGT) [2]. Due to the lower temperature heat (550ºC) required, the hybrid Cu-Cl cycle is one of the most promising thermochemical cycles
for hydrogen production using nuclear or solar heat.  The cycle can be coupled
with several types of nuclear reactors, e.g., the supercritical water reactor
being developed in Canada, CANDU Mark 2, the sodium cooled reactor, or the high
temperature gas reactor with the high temperature heat being used for
electricity generation.  Several types of solar devices can also be used, e.g.,
a power tower with molten salt as a heat storage medium or a concentrator.  The
lower temperature should mitigate some of the demands on the materials of
construction. 

The copper-chlorine cycle consists of the three major reactions
shown in Table 1. The electrolysis reaction (1) in which cupric chloride (CuCl2) is produced at
the anode and H2 at the cathode is carried out electrochemically.
The CuCl2(a) from (1) is hydrolyzed to copper oxychloride (Cu2OCl2)
according to the hydrolysis reaction (2). Molten cuprous chloride (CuCl)
is then produced from the decomposition reaction (3).

Table 1. Reactions in the Copper-Chlorine Cycle

Reaction                                                          
                                                                                   Conditions

(1) Electrolysis/Hydrogen
formation: CuCl(a) + HCl(a) + 2H2O → CuCl2·2H2O(a)
+ ½ H2(g)  100ºC, 24 bar

(2) Hydrolysis/HCl
formation: 2 CuCl2(s) + H2O(g) → Cu2OCl2(s)
+ 2HCl(g)                            400ºC, 1 bar

(3) Decomposition/Oxygen formation: Cu2OCl2(s)
→ ½ O2(g) + 2CuCl(s)                                540ºC, 1
bar

All reactions have been experimentally demonstrated in
proof-of-concept work. The electrolytic reaction (1) was demonstrated at
the Atomic Energy of Canada, Ltd. (AECL) recently. Meeting performance (500
mA/cm2 at 0.5V) and cost target ($2500/m2) is the primary
challenge for the electrolysis reaction. The two thermal reactions, the
hydrolysis of CuCl2(2), and the decomposition of Cu2OCl2(3) are being investigated in more detail to facilitate an engineering
lab-scale demonstration.

We consider the hydrolysis reaction to be
the most challenging reaction because of two factors: (i) a competing reaction
of CuCl2 and (ii) the need for excess water.

The competing reaction is the thermal decomposition of CuCl2:

2CuCl2 (s) → 2CuCl (s) + Cl2 (g)                                                                     (4)

 

Because CuCl is a product of the subsequent reaction, this
competing reaction is not a showstopper, provided the chlorine can be scavenged
and the amount of chlorine formed is minimal. We believe that this competing
reaction can be minimized by the choice of operating conditions and the reactor
design.

Early work has shown that fixed bed reactor designs are not
optimal. Inefficiencies in heat and mass transfer inhibited the desired
reaction. Unreacted CuCl2 was observed and this material tended to
be agglomerated in the middle of the fixed bed. Under these conditions, the
decomposition of CuCl2 to form CuCl (4) was enhanced.

To improve mass and heat transfer and inhibit the decomposition
reaction, a spray reactor was designed.  In this concept, a solution of CuCl2
is injected into the reactor into a hot zone at 375-400ºC using a nebulizer. This
new reactor design should provide better mass transfer since CuCl2
and water are injected together. The nebulizer produces a very fine mist of
CuCl2 droplets when an inert gas with a flow rate of 100-300 ml/min
is used. The engineering lab-scale reactor has an ID of 4.75 in and is held in
a 36-in long heated zone. The solid products of the reaction are collected at
the bottom of the reactor which is maintained at a lower temperature (around 100-200ºC)
to prevent further reaction. Superheated steam is added to improve heat
transfer either at the top (co-current flow) or at the bottom of the reactor
(counter-current flow). The preliminary
test results are encouraging. Very fine black particles were found at the
bottom of the reactor. X-ray diffraction was used to identify the phases.  In
most patterns, Cu2OCl2 was the predominant phase. 
However, some unreacted CuCl2 and possibly CuCl were also
identified.  The effect of various operating parameters,
e.g., the inert gas flowrate in the nebulizer and in the superheated steam
line, the CuCl2 solution flowrate, and the current flow designs are being
investigated with respect to Cu2OCl2 and CuCl formation.

1.     
McQuillan, B.W., Brown, L.C.,
Besenbruch, G.E., Tolman, R. Cramer, T., Russ, B.E, Vermillion, B.A., Earl, B.,
Hsieh, H.-T., Chen, Y., Kwan, K., Diver, R. Siegal, N., Weimer, A., Perkins,
C., Lewandowski, A., High Effiiency Generation of Hydrogen Fuels using Solar
Thermochemical Splitting of Water, Annual Report, GA-A24972, General Atomics,
San Diego, CA (2005).

2.     
Carty, R.H., Mazumder, M.M., Schreiber,
J.D., and Pangborn, J.B., Thermochemical Hydrogen Production, Report GRI-80/0023.4,
Institute of Gas Technology, Chicago, IL (1981).

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