The present invention provides a method for capturing Carbon Dioxide (CO2) from flue gas & waste gas streams in to liquid at a high efficiency (or at a required efficiency) without the need for liquid or aqueous reagents such as Amines and Carbonates.
Currently in order to fulfil the requirement for higher efficiency carbon capture, thus enabling useful transfer to products or storage in a more manageable form, chemical reactions which enhance liquid absorption of CO2 by reacting with it within the liquid interface are widely employed.
Once captured the CO2 may have to be released into a more concentrated stream such that it becomes necessary to reverse the chemical reaction which binds it (e.g. K2CO3(aq)+CO2(aq)+H2O(1)=2KHCO3(aq)). This is another costly step, which is facilitated by changes in pressure, temperature or chemical equilibrium or by applying a second reagent to ‘unlock’ the CO2 and release it in a more usable state.
Typically CO2 recovered in carbon capture plants can be used for Enhanced Oil Recovery or for Growth Enhancement of horticultural crops, fruits & flowers in glass-houses.
By combining the unique properties of counter-current fluidised bed gas scrubbers, which employ fluidisable elements, being hollow or low density solid elements, usually manufactured in plastic materials, with the use of non-reacting salt or saline solutions, a more advantageous result is achieved.
The result is a surprisingly efficient method for capturing carbon and quickly releasing it (from a fluidised bed or other desorber or stripper), which overcomes the need for expensive consumable reagents or application of heat, pressure and additives for CO2 release and reagent regeneration purposes.
The unique properties of fluid bed gas scrubbers that allow the combinatory effects to function are;
By applying these advantages in combination with the use of salt solutions in water it becomes possible to raise capture efficiencies (CO2 removal percentage) to well above 50%, which is otherwise not achievable except by employing costly and inherently complicated reacting systems.
Typically salt or saline solutions can include any dissolvable salt up to, and even beyond, its solubility limit such that the solution is maintained at saturation. The important thing is to use an existing saline solution such as brackish or sea water or to increase the salt concentration of a town or process water such that the Ionic Strength of the solution has at least a value of 0.2 mol/litre.
In addition to the requirement for elevated salt concentration, other simultaneous conditions are needed to create the required high removal efficiencies (typically greater than 10% absorption is needed for most applications using CO2) are to have CO2(g) partial pressures in gas above 1% v/v and L/G ratios, litres/m3, in excess of 20.
At L/G ratios at this level packed towers and sieve plate or tray columns would flood and spray towers would give insufficient interphase surface between the ascending gas and the descending liquid within the scrubber body.
Soluble salts that can be used to boost the Ionic Strength of the resultant saline solution include Chlorides, Bromides, Iodides, Chlorates, Sulphates, Sulphides, Sulfites, Bicarbonates & Phosphates and even Hydroxides & Carbonates which react with CO2(aq). However, when using rapid desorption (stripping), as in the arrangement
A few examples of appropriate salts are CaCl2, NaCl, KCl, K2CO3, KHCO3, Na2CO3, NaHCO3, CaCO3, Ca(HCO3)2.
Thus, the present invention provides an improved process for carbon capture in accordance with the Claims appended hereto.
There now follows a detailed description of the invention, which is to be read with reference to the accompanying drawings in which:
The CO2 was captured in to a semi saturated aqueous solution of Calcium Chloride of about 50% of its pure CaCl2(aq) solubility limit in water at 12° C., (i.e. at about 31.5 g of CaCl2(c) per 100 g of water or 2.84 mol/litre) being the average temperature of the tested saline solution through the scrubber tower, the saline solution having an Ionic Strength of about 8.5 mol/litre.
Other fluidised bed elements are able to generate higher interfacial areas and, hence, greater capture efficiencies and lower pressure drops.
One proposed application of the process is shown in
Another proposed application of the novel process provided by the present invention is illustrated in
The Turboscrubber® is provided with:
The Algae tank 7 comprises an optional stirrer 9, a bleed valve 8 and on outlet line with a return pump 10 in a line 10a for recirculating treated flue gas to the Turboscrubber® 2.
An optional Algae recycling line 4 is provided between the line 5 and the recirculating line 10a, see
Modifications may be made to the above described development within the scope of the Claims appended hereto.
Number | Date | Country | Kind |
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1505737.5 | Apr 2015 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/GB2016/000057 | 3/22/2016 | WO | 00 |