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1. Introduction - Firenze University Press

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Abstract:<br />

PROCEEDINGS OF ECOS 2012 - THE 25 TH INTERNATIONAL CONFERENCE ON<br />

EFFICIENCY, COST, OPTIMIZATION, SIMULATION AND ENVIRONMENTAL IMPACT OF ENERGY SYSTEMS<br />

JUNE 26-29, 2012, PERUGIA, ITALY<br />

Influence of regeneration condition on cyclic CO2<br />

capture using pre-treated dispersed CaO as high<br />

temperature sorbent<br />

Stendardo Stefano a , Calabrò Antonio a<br />

a ENEA, Italian National Agency for New Technologies, Energy, and the Sustainable Economic<br />

Development Via Anguillarese, 301, S. Maria di Galeria, 00123, Rome, Italy<br />

In this experimental investigation the effect of calcination temperature and atmosphere composition on CO2<br />

uptake of a solid sorbent have been analysed. The sorbent were synthesized by means of a CaO hydrolysis<br />

technique to generate sorbents with 75% and 85% of active phase CaO. The material at hand also contains<br />

a calcium aluminate phase acting as a binder of the active phase. Pre-treatment was accomplished in a<br />

thermo-gravimetric analyser (TGA) exposed in an atmosphere of 86% N2 and 14% CO2 under 600 °C. The<br />

as-synthesised sorbent and the pre-treated sorbent have been characterised by scanning electron<br />

microscope, nitrogen physic-sorption tests, and multi-cycling carbonation-calcination test in TGA (160<br />

cycles). Here, the CO2 uptake took place at programmed temperature (600 °C) with three different<br />

regeneration condition tested:<br />

a) mild condition: regeneration under 900 °C with 14% CO2 and 86 % N2;<br />

b)moderately severe condition: regeneration under 1000 °C with 14% CO2 and 86 % N2;<br />

c) severe condition: regeneration under 1000 °C with 86% CO2 and 14 % N2.<br />

The experimental results show significant improvement in the stability of the CO2 uptake capacity over<br />

multiple cycles when comparing the synthetic sorbents to natural dolomite. For an instance, the 75% CaO<br />

synthetic sorbent shows a good reversibility for the CO2 uptake (0.13 g-CO2/g-sor) up to 150th cycle under<br />

severe condition.<br />

Keywords:<br />

Keywords: solid sorbent, carbon capture, carbonate chemical looping, self-reactivation.<br />

<strong>1.</strong> <strong>Introduction</strong><br />

Carbon capture technologies are expected to be a promising route to meet the objective of a low<br />

carbon electricity production and the increasing of coal foreseen by the scientific and industrial<br />

community. Hydrogen production from renewable energy sources, coal and biomass is a priority for<br />

Italian medium and long term energy policy. Thus, in Italy technologies for CO2 capture are<br />

considered a main topic to be studied and demonstrated, and represent a significant opportunity for<br />

industries. In order to promote carbon capture technologies, ENEA has constructed an experimental<br />

platform, named ZECOMIX, to investigate both the gasification of coal and the separation of CO2<br />

from synthetic gas fuel or flue gas. Particularly the decarbonisation of the gaseous stream happens<br />

by means of a carbonate looping (CaL) technology with a CaO based solid sorbent. When the CaO<br />

is converted to the calcium carbonate, the spent solid sorbent is sent back to the regeneration<br />

process where an active sorbent is regenerated for a new carbonate looping. As reported in the<br />

scientific literature: [1-4], when naturally occurring material as calcite or dolomite are used as CO2<br />

acceptor in a CaL, there is a decay of reversibility. The ideal CO2 sorbent in a CaL should show a<br />

number of properties: high and stable CO2 uptake capacity throughout continuous decarbonisingregeneration<br />

cycling, fast reaction kinetics, uptake capacity and kinetics close to theoretical<br />

maximum values, and also mechanical stability and sintering resistance. In an attempt to achieve<br />

this goal, researchers have developed novel synthetic sorbents based on e.g. CaO dispersed on<br />

calcium aluminate ceramic supports. [5]. In this work a number of experimental results on the<br />

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