WO2011089292A1 - Capture et séquestration de co2 par carbonatation de résidus céramiques - Google Patents

Capture et séquestration de co2 par carbonatation de résidus céramiques Download PDF

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Publication number
WO2011089292A1
WO2011089292A1 PCT/ES2011/000015 ES2011000015W WO2011089292A1 WO 2011089292 A1 WO2011089292 A1 WO 2011089292A1 ES 2011000015 W ES2011000015 W ES 2011000015W WO 2011089292 A1 WO2011089292 A1 WO 2011089292A1
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WO
WIPO (PCT)
Prior art keywords
capture
sequestration
ceramic
ceramic waste
carbonation
Prior art date
Application number
PCT/ES2011/000015
Other languages
English (en)
Spanish (es)
Inventor
Emilio Galan Huertos
Patricia Aparicio Fernandez
Original Assignee
Universidad De Sevilla
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Universidad De Sevilla filed Critical Universidad De Sevilla
Publication of WO2011089292A1 publication Critical patent/WO2011089292A1/fr

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/62Carbon oxides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/40Alkaline earth metal or magnesium compounds
    • B01D2251/402Alkaline earth metal or magnesium compounds of magnesium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/40Alkaline earth metal or magnesium compounds
    • B01D2251/404Alkaline earth metal or magnesium compounds of calcium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/50Carbon oxides
    • B01D2257/504Carbon dioxide
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/20Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00Capture or disposal of greenhouse gases
    • Y02C20/40Capture or disposal of greenhouse gases of CO2

Definitions

  • the invention is aimed at capturing and sequestering C0 2 in ceramic materials from construction waste. These materials react directly with C0 2 in the presence of water producing carbonates, so that C0 2 is permanently stabilized.
  • the present invention has a double environmental application: on the one hand, there is a reduction in atmospheric C0 2 since it would be injected into ceramic waste from the construction and on the other, the negative landscape impact caused by the ceramic waste from the construction would be reduced .
  • C0 2 The capture and storage of C0 2 (CAC or CCS "carbon capture sequestration") is considered one of the options to reduce the emissions of C0 2 generated by human activities.
  • Other technological options are the following: 1) the reduction of energy demand by increasing the efficiency of energy conversion and / or use devices; 2) the decarbonisation of the energy supply (opting for fuels with less carbon, for example, replacing coal with natural gas), and / or increasing the use of renewable energy sources and / or nuclear energy (which, in definitively, they emit scarce amounts, if any, of C0 2 ); 3) the sequestration of C0 2 through the improvement of natural sinks through biological fixation; and 4) the reduction of greenhouse gases other than C0 2 .
  • the CAC or CCS (Carbon Capture and Storage) is probably the biggest geotechnological challenge of the 21st century.
  • the CAC first involves the use of technologies to collect and concentrate the C0 2 produced in industrial sources, then transport it to an appropriate storage location and then store it isolating it from the atmosphere for a long period of time.
  • geological formations and structures most conducive to the deep storage of C0 2 have been widely documented in the scientific and technical literature generated in recent years: 1) coal layers rich in methane, 2) depleted or depleted deposits of hydrocarbons (oil and gas), 3) deep saline aquifers, and 4) cavities in salt formations.
  • the first three types are postulated as more prominent objectives, although their presence and storage capacity, that is, their dimensions, are conditioned by the specific geological features of each territory.
  • Other possible formations or geological structures represent storage options that have not yet been studied enough to be able to assess their potential today.
  • the purpose of this invention is to propose the injection of C0 2 into quarries and gravels recovered with RDC. For it is part of laboratory experiments on ceramic materials and C0 2 in different environmental conditions. It has been shown that in the presence of water carbonation process is a direct flow of C0 2 at low pressure ( ⁇ 20 bar). Experiences have been carried out with CC1 ⁇ 2 in a supercritical state and it has been proven that the carbonation process has a lower yield.
  • Figure 1 X-ray diffraction diagrams showing the variation of the calcite content from the initial sample (black diagram), to the final sample (blue diagram) after 65 h of reaction with C0 2 in the presence of 10% water
  • the present invention aims at capturing and sequestering C0 2 in ceramic materials from construction waste.
  • these materials react directly with C0 2 producing carbonates, so that carbon dioxide is fixed permanently.
  • the presence of water is essential for such a carbonation reaction to occur in ceramic materials, the proportion of water having to vary between 5 and 30% by weight depending on the composition and manufacturing temperature of the structural ceramics.
  • These ceramic materials are manufactured from common clays in a temperature range of 800 ° C-1100 ° C.
  • These ceramic materials are injected with low pressure C0 2 (with an injection pressure of C0 2 varying between 0.5 and 80 bar, the highest yields at pressures of C0 2 ⁇ 20 bar) with which it reacts chemically always in the presence of water giving rise to carbonates, so it is permanently fixed.
  • reaction yield is higher at low pressures of C0 2, so it is not necessary to reach large pressures of C0 2 and therefore, to store at 800m depth as required by other C0 2 capture alternatives
  • the raw material is based on a mixture of common clays containing 30% carbonates (calcite and dolomite), 30% quartz, 37% phyllosilicates and 3% feldspars. This raw material is cooked at 850 ° C, the result being a ceramic product structural that contains 5% calcite, together with high temperature minerals and oxides of Ca and Mg.
  • a mixture of this ceramic product is prepared with water (10% by weight) and a current of 1 bar of C0 2 is applied at a temperature of 30 ° C for 65 hours.
  • the content of calcite increases from 5% to more than 15% by weight, due to the carbonation produced after reacting the calcium present (obviously not in the form of calcite) with C0 2 in the presence of water.
  • this reaction should be reproduced in an X-ray diffractometer equipped with a reaction chamber and a phase quantification procedure based on Rietveld refinement (for example TOPAS) be applied.
  • the first diagram corresponds to that of the original sample (in black).
  • the following diagrams correspond to the products formed after adding water and injecting the current of C0 2 .
  • the pink diagram corresponds to a reaction time of 24 hours. The following were obtained every 1.5 hours, and so on until the total reaction time was 65 hours (blue diagram).
  • the results of the quantitative analysis appear in Table 1.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Environmental & Geological Engineering (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)
  • Treating Waste Gases (AREA)

Abstract

L'invention a pour objet la capture et la séquestration de CO2 dans des matériaux céramiques issus de résidus de la construction. Ces matériaux réagissent directement avec le CO2 en présence d'eau, produisant des carbonates, de sorte que le CO2 se stabilise de manière permanente. La présente invention présente une double application environnementale: d'une part, il se produit une réduction du CO2 atmosphérique étant donné qu'il est injecté dans des résidus céramiques issus de la construction et d'autre part, l'impact négatif sur le paysage causé par les résidus céramiques de la construction sont réduits.
PCT/ES2011/000015 2010-01-25 2011-01-25 Capture et séquestration de co2 par carbonatation de résidus céramiques WO2011089292A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ESP201000084 2010-01-25
ES201000084A ES2364421B2 (es) 2010-01-25 2010-01-25 Captura y secuestro de co2 mediante la carbonatación de residuos cerámicos.

Publications (1)

Publication Number Publication Date
WO2011089292A1 true WO2011089292A1 (fr) 2011-07-28

Family

ID=44306418

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/ES2011/000015 WO2011089292A1 (fr) 2010-01-25 2011-01-25 Capture et séquestration de co2 par carbonatation de résidus céramiques

Country Status (2)

Country Link
ES (1) ES2364421B2 (fr)
WO (1) WO2011089292A1 (fr)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090143211A1 (en) * 2007-11-15 2009-06-04 Rutgers, The State University Of New Jersey Systems and methods for carbon capture and sequestration and compositions derived therefrom
US20090202410A1 (en) * 2008-02-12 2009-08-13 Michigan Technology University Capture and Sequestration of Carbon Dioxide in Flue Gases

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090143211A1 (en) * 2007-11-15 2009-06-04 Rutgers, The State University Of New Jersey Systems and methods for carbon capture and sequestration and compositions derived therefrom
US20090202410A1 (en) * 2008-02-12 2009-08-13 Michigan Technology University Capture and Sequestration of Carbon Dioxide in Flue Gases

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
FERNANDEZ BERTOS ET AL.: "A review of accelerated carbonation technology in the treatment of cement-based materials and sequestration of C02.", JOURNAL OF HAZARDOUS MATERIALS, vol. B112, 2004, pages 193 - 205 *
IIZUKA ET AL.: "Development of a New C02 Sequestration Process Utilizing the Carbonation of Waste Cement.", IND. ENG. CHEM.RES, vol. 43, 2004, pages 7880 - 7887 *
STOLAROFF ET AL.: "Using CaO- and MgO-rich industrial waste streams for carbon sequestration.", ENERGY CONVERSION AND MANAGEMENT, vol. 46, no. 5, March 2005 (2005-03-01), pages 687 - 699, XP004678769 *

Also Published As

Publication number Publication date
ES2364421B2 (es) 2012-01-26
ES2364421A1 (es) 2011-09-02

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