Probing Surface Transformations of Lanthanum Nickelate Electrocatalysts during Oxygen Evolution Reaction.

Monitoring the spontaneous reconstruction of the surface of metal oxides under electrocatalytic reaction conditions is critical to identifying the active sites and establishing structure-activity relationships. Here, we report on a self-terminated surface reconstruction of Ruddlesden-Popper lanthanum nickel oxide (La2NiO4+δ) that occurs spontaneously during reaction with alkaline electrolyte species. Using a combination of high-resolution scanning transmission electron microscopy (HR-STEM), surface-sensitive X-ray photoelectron spectroscopy (XPS), and soft X-ray absorption spectroscopy (sXAS), as well as electrochemical techniques, we identify the structure of the reconstructed surface layer as an amorphous (oxy)hydroxide phase that features abundant under-coordinated nickel sites. No further amorphization of the crystalline oxide lattice (beyond the ∼2 nm thick layer formed) was observed during oxygen evolution reaction (OER) cycling experiments. Notably, the formation of the reconstructed surface layer increases the material's oxygen evolution reaction (OER) activity by a factor of 45 when compared to that of the pristine crystalline surface. In contrast, a related perovskite phase, i.e., LaNiO3, did not show noticeable surface reconstruction, and also no increase in its OER activity was observed. This work provides detailed insight into a surface reconstruction behavior dictated by the crystal structure of the parent oxide and highlights the importance of surface dynamics under reaction conditions.

Of Glasses and Crystals: Mitigating the Deactivation of CaO-Based CO2 Sorbents through Calcium Aluminosilicates.

CaO-based sorbents are cost-efficient materials for high-temperature CO2 capture, yet they rapidly deactivate over carbonation-regeneration cycles due to sintering, hindering their utilization at the industrial scale. Morphological stabilizers such as Al2O3 or SiO2 (e.g., introduced via impregnation) can improve sintering resistance, but the sorbents still deactivate through the formation of mixed oxide phases and phase segregation, rendering the stabilization inefficient. Here, we introduce a strategy to mitigate these deactivation mechanisms by applying (Al,Si)Ox overcoats via atomic layer deposition onto CaCO3 nanoparticles and benchmark the CO2 uptake of the resulting sorbent after 10 carbonation-regeneration cycles against sorbents with optimized overcoats of only alumina/silica (+25%) and unstabilized CaCO3 nanoparticles (+55%). 27Al and 29Si NMR studies reveal that the improved CO2 uptake and structural stability of sorbents with (Al,Si)Ox overcoats is linked to the formation of glassy calcium aluminosilicate phases (Ca,Al,Si)Ox that prevent sintering and phase segregation, probably due to a slower self-diffusion of cations in the glassy phases, reducing in turn the formation of CO2 capture-inactive Ca-containing mixed oxides. This strategy provides a roadmap for the design of more efficient CaO-based sorbents using glassy stabilizers.

Deciphering the structural dynamics in molten salt-promoted MgO-based CO2 sorbents and their role in the CO2 uptake.

The development of effective CO2 sorbents is vital to achieving net-zero CO2 emission targets. MgO promoted with molten salts is an emerging class of CO2 sorbents. However, the structural features that govern their performance remain elusive. Using in situ time-resolved powder x-ray diffraction, we follow the structural dynamics of a model NaNO3-promoted, MgO-based CO2 sorbent. During the first few cycles of CO2 capture and release, the sorbent deactivates owing to an increase in the sizes of the MgO crystallites, reducing in turn the abundance of available nucleation points, i.e., MgO surface defects, for MgCO3 growth. After the third cycle, the sorbent shows a continuous reactivation, which is linked to the in situ formation of Na2Mg(CO3)2 crystallites that act effectively as seeds for MgCO3 nucleation and growth. Na2Mg(CO3)2 forms due to the partial decomposition of NaNO3 during regeneration at T ≥ 450°C followed by carbonation in CO2.

Altering Oxygen Binding by Redox-Inactive Metal Substitution to Control Catalytic Activity: Oxygen Reduction on Manganese Oxide Nanoparticles as a Model System.

Establishing generic catalyst design principles by identifying structural features of materials that influence their performance will advance the rational engineering of new catalytic materials. In this study, by investigating metal-substituted manganese oxide (spinel) nanoparticles, Mn3 O4 :M (M=Sr, Ca, Mg, Zn, Cu), we rationalize the dependence of the activity of Mn3 O4 :M for the electrocatalytic oxygen reduction reaction (ORR) on the enthalpy of formation of the binary MO oxide, Δf H°(MO), and the Lewis acidity of the M2+ substituent. Incorporation of elements M with low Δf H°(MO) enhances the oxygen binding strength in Mn3 O4 :M, which affects its activity in ORR due to the established correlation between ORR activity and the binding energy of *O/*OH/*OOH species. Our work provides a perspective on the design of new compositions for oxygen electrocatalysis relying on the rational substitution/doping by redox-inactive elements.

From ethene to propene (ETP) on tailored silica-alumina supports with isolated Ni(ii) sites: uncovering the importance of surface nickel aluminate sites and the carbon-pool mechanism.

Catalysts with well-defined isolated Ni(ii) surface sites have been prepared on three silica-based supports. The outer shells of the support were comprised either of an amorphous aluminosilicate or amorphous alumina (AlO x ) layer - associated with a high and low density of strong Brønsted acid sites (BAS), respectively. When tested for ethene-to-propene conversion, Ni catalysts with a higher density of strong BAS demonstrate a higher initial activity and productivity to propene. On all three catalysts, the propene productivity correlates closely with the concentration of C8 aromatics, suggesting that propene may form via a carbon-pool mechanism. While all three catalysts deactivate with time on stream, the deactivation of catalysts with Ni(ii) sites on AlO x , i.e., containing surface Ni aluminate sites, is shown to be reversible by calcination (coke removal), in contrast to the deactivation of surface Ni silicate or aluminosilicate sites, which deactivate irreversibly by forming Ni nanoparticles.

Yolk-shell-type CaO-based sorbents for CO2 capture: assessing the role of nanostructuring for the stabilization of the cyclic CO2 uptake.

Improving the cyclic CO2 uptake stability of CaO-based solid sorbents can provide a means to lower CO2 capture costs. Here, we develop nanostructured yolk(CaO)-shell(ZrO2) sorbents with a high cyclic CO2 uptake stability which outperform benchmark CaO nanoparticles after 20 cycles (0.17 gCO2 gSorbent-1) by more than 250% (0.61 gCO2 gSorbent-1), even under harsh calcination conditions (i.e. 80 vol% CO2 at 900 °C). By comparing the yolk-shell sorbents to core-shell sorbents, i.e. structures with an intimate contact between the stabilizing phase and CaO, we are able to identify the main mechanisms behind the stabilization of the CO2 uptake. While a yolk-shell architecture stabilizes the morphology of single CaO nanoparticles over repeated cycling and minimizes the contact between the yolk and shell materials, core-shell architectures lead to the formation of a thick CaZrO3-shell around CaO particles, which limits CO2 transport to unreacted CaO. Hence, yolk-shell architectures effectively delay CaZrO3 formation which in turn increases the theoretically possible CO2 uptake since CaZrO3 is CO2-capture-inert. In addition, we observe that yolk-shell architectures also improved the carbonation kinetics in both the kinetic- and diffusion-controlled regimes leading to a significantly higher cyclic CO2 uptake for yolk-shell-type sorbents.

Na2CO3-modified CaO-based CO2 sorbents: the effects of structure and morphology on CO2 uptake.

Calcium looping (CaL) is a CO2 capture technique based on the reversible carbonation/calcination of CaO that is considered promising to reduce anthropogenic CO2 emissions. However, the rapid decay of the CO2 uptake of CaO over repeated cycles of carbonation and calcination due to sintering limits its implementation at the industrial scale. Thus, the development of material design strategies to stabilize the CO2 uptake capacity of CaO is paramount. The addition of alkali metal salts to CaO has been proposed as a strategy to mitigate the rapid loss of its cyclic CO2 uptake capacity. However, there are conflicting results concerning the effect of the addition of alkali metal carbonates on the structure and CO2 capacity of CaO. In this work, we aim at understanding the effect of the addition of Na2CO3 to CaO on the sorbent's structure and its CO2 uptake capacity. We demonstrate that under industrially-relevant conditions the addition of as little as 1 wt% of Na2CO3 reduces severely the CO2 uptake of CaO. Combining TGA, XAS and FIB-SEM analysis allowed us to attribute the performance degradation to the formation of the double salt Na2Ca(CO3)2 that induces strong sintering leading to a significant loss in the sorbent's pore volume. In addition, during the carbonation step the formation of a dense layer of Na2Ca(CO3)2 that covers unreacted CaO prevents its full carbonation to CaCO3.

Comprehensive Biological Evaluation of Biomaterials Used in Spinal and Orthopedic Surgery.

Biological acceptance is one of the most important aspects of a biomaterial and forms the basis for its clinical use. The aim of this study was a comprehensive biological evaluation (cytotoxicity test, bacterial colonization test, blood platelets adhesion test and transcriptome and proteome analysis of Saos-2 cells after contact with surface of the biomaterial) of biomaterials used in spinal and orthopedic surgery, namely, Ti6Al4V ELI (Extra Low Interstitials), its modified version obtained as a result of melting by electron beam technology (Ti6Al4V ELI-EBT), polyether ether ketone (PEEK) and polished medical steel American Iron and Steel Institute (AISI) 316L (the reference material). Biological tests were carried out using the osteoblasts-like cells (Saos-2, ATCC HTB-85) and bacteria Escherichia coli (DH5α). Results showed lack of cytotoxicity of all materials and the surfaces of both Ti6Al4V ELI and PEEK exhibit a significantly higher resistance to colonization with E. coli cells, while the more porous surface of the same titanium alloy produced by electron beam technology (EBT) is more susceptible to microbial colonization than the control surface of polished medical steel. None of the tested materials showed high toxicity in relation to E. coli cells. Susceptibility to platelet adhesion was very high for polished medical steel AISI 316L, whilst much lower for the other biomaterials and can be ranked from the lowest to the highest as follows: PEEK < Ti6Al4V ELI < Ti6Al4V ELI-EBT. The number of expressed genes in Saos-2 cells exposed to contact with the examined biomaterials reached 9463 genes in total (ranging from 8455 genes expressed in cells exposed to ELI to 9160 genes in cells exposed to PEEK). Whereas the number of differentially expressed proteins detected on two-dimensional electrophoresis gels in Saos-2 cells after contact with the examined biomaterials was 141 for PEEK, 223 for Ti6Al4V ELI and 133 for Ti6Al4V ELI-EBT. Finally, 14 proteins with altered expression were identified by mass spectrometry. In conclusion, none of the tested biomaterials showed unsatisfactory levels of cytotoxicity. The gene and protein expression analysis, that represents a completely new approach towards characterization of these biomaterials, showed that the polymer PEEK causes much more intense changes in gene and protein expression and thus influences cell metabolism.

Single Site Cobalt Substitution in 2D Molybdenum Carbide (MXene) Enhances Catalytic Activity in the Hydrogen Evolution Reaction.

Two-dimensional (2D) carbides, nitrides, and carbonitrides known as MXenes are emerging materials with a wealth of useful applications. However, the range of metals capable of forming stable MXenes is limited mostly to early transition metals of groups 3-6, making the exploration of properties inherent to mid or late transition metal MXenes very challenging. To circumvent the inaccessibility of MXene phases derived from mid-to-late transition metals, we have developed a synthetic strategy that allows the incorporation of such transition metal sites into a host MXene matrix. Here, we report the structural characterization of a Mo2CTx:Co phase (where Tx are O, OH, and F surface terminations) that is obtained from a cobalt-substituted bulk molybdenum carbide (ß-Mo2C:Co)  through a two-step synthesis: first an intercalation of gallium yielding Mo2Ga2C:Co followed by removal of Ga via HF treatment. Extended X-ray absorption fine structure (EXAFS) analysis confirms that Co atoms occupy Mo positions in the Mo2CTx lattice, providing isolated Co centers without any detectable formation of other cobalt-containing phases. The beneficial effect of cobalt substitution on the redox properties of Mo2CTx:Co is manifested in a substantially improved hydrogen evolution reaction (HER) activity, as compared to the unsubstituted Mo2CTx catalyst. Density functional theory (DFT) calculations attribute the enhanced HER kinetics of Mo2CTx:Co to the favorable binding of hydrogen on the oxygen terminated MXene surface that is strongly influenced by the substitution of Mo by Co in the Mo2CTx lattice. In addition to the remarkable HER activity, Mo2CTx:Co features excellent operational and structural stability, on par with the best performing non-noble metal-based HER catalysts. Overall, our work expands the compositional space of the MXene family by introducing a material with site-isolated cobalt centers embedded in the stable matrix of Mo2CTx. The synthetic approach presented here illustrates that tailoring the properties of MXenes for a specific application can be achieved via substitution of the host metal sites by mid or late transition metals.

Cadaveric biomechanical testing of torque - to - failure magnitude of Bilateral Apical Vertebral Derotation maneuver in the thoracic spine.

It remains unclear what is the real safe limit of torque magnitude during Bilateral Apical Vertebral Derotation (BAVD) in thoracic curve correction. Up to author's knowledge there is no study except this one, to reproduce in-vivo real measurements and intraoperative conditions during BAVD maneuver. The objective of this study was to evaluate the torsional strength of the instrumented thoracic spine under axial rotation moment as well as to define safety limits under BAVD corrective maneuver in scoliosis surgery. 10 fresh, full-length, young and intact human cadavers were tested. After proper assembly of the apparatus, the torque was applied through its apical part, simulating thoracic curve derotation. During each experiment the torque magnitude and angular range of derotation were evaluated. For more accurate analysis after every experiment the examined section of the spine was resected from the cadaver and evaluated morphologically and with a CT scan. The average torque to failure during BAVD simulation was 73,3 ± 5,49Nm. The average angle of BAVD to failure was 44,5 ± 8,16°. The majority of failures were in apical area. There was no significant difference between the fracture occurrence of left or right side of lateral wall of the pedicle. There was no spinal canal breach and/or medial wall failure in any specimen. The safety limits of thoracic spine and efficacy of BAVD for axial plane correction in the treatment of Adolescent Idiopathic Scoliosis (AIS) were established. It provided qualitative and quantitative information essential for the spinal derotation under safe loading limits.

Reversible Exsolution of Dopant Improves the Performance of Ca2Fe2O5 for Chemical Looping Hydrogen Production.

Hydrogen (H2) is a clean energy carrier and a major industrial feedstock, e.g., to produce ammonia and methanol. High-purity H2 can be produced efficiently from methane (CH4) using chemical looping-based approaches. In this work, we report on the development of a calcium-iron-based oxygen carrier (Ca2Fe2O5) doped with Ni or Cu and investigate its redox performance for H2 production when CH4 is used as the fuel. The experimental results suggest that the rapid formation of metallic Ni or Cu through exsolution promotes the reducibility of Ca2Fe2O5 with CH4. It was found that the reversible exsolution of Ni or Cu nanoparticles and their reincorporation in the Ca2Fe2O5 structure is key to avoid particle sintering and deactivation. Having the potential of converting a larger fraction of steam to H2 than pure iron oxide in addition to its higher reactivity with CH4, the doped calcium-iron-based oxygen carrier is a promising material for chemical looping H2 production.

Optimization of the structural characteristics of CaO and its effective stabilization yield high-capacity CO2 sorbents.

Calcium looping, a CO2 capture technique, may offer a mid-term if not near-term solution to mitigate climate change, triggered by the yet increasing anthropogenic CO2 emissions. A key requirement for the economic operation of calcium looping is the availability of highly effective CaO-based CO2 sorbents. Here we report a facile synthesis route that yields hollow, MgO-stabilized, CaO microspheres featuring highly porous multishelled morphologies. As a thermal stabilizer, MgO minimized the sintering-induced decay of the sorbents' CO2 capacity and ensured a stable CO2 uptake over multiple operation cycles. Detailed electron microscopy-based analyses confirm a compositional homogeneity which is identified, together with the characteristics of its porous structure, as an essential feature to yield a high-performance sorbent. After 30 cycles of repeated CO2 capture and sorbent regeneration, the best performing material requires as little as 11 wt.% MgO for structural stabilization and exceeds the CO2 uptake of the limestone-derived reference material by ~500%.

The effect of copper on the redox behaviour of iron oxide for chemical-looping hydrogen production probed by in situ X-ray absorption spectroscopy.

The production of high purity hydrogen with the simultaneous capture of CO2, can be achieved through a chemical looping (CL) cycle relying on an iron oxide-based oxygen carrier. Indeed, the availability of active and cyclically stable oxygen carriers is a key criterion for the practical implementation of this technology. In this regard, improving our understanding of the reduction pathway(s) of iron-based oxygen carriers and the development of concepts to increase the reduction kinetics are important aspects. The aim of this work is to evaluate the effect of the addition of copper on the redox behaviour of iron oxide based oxygen carriers stabilized on ZrO2. In situ pulsed-H2 XANES (Fe K-edge) experiments allowed for the determination of the reduction pathways in these materials, viz. the reduction of both Fe2O3 and CuFe2O4 proceeded via a Fe2+ intermediate: Fe2O3 (CuFe2O4) → Fe3O4 (Cu0) → FeO (Cu0) → Fe0 (Cu0). In the first step CuFe2O4 is reduced to Cu0 and Fe3O4, whereby Cu0 promotes the further reduction of iron oxide, increasing their rate of formation. In particular, the rate of reduction of FeO → Fe0 is accelerated most dramatically by Cu0. This is an encouraging result as the FeO → Fe0 transition is the slowest reduction reaction.

In vitro simulation of intraoperative vertebroplasty applied for pedicle screw augmentation. A biomechanical evaluation.

BACKGROUND AND PURPOSE: The purpose of this study was to evaluate the effect of an in vitro simulation of intraoperative vertebroplasty on embedded pedicle screws resistance to pullout. This method involved an application of acrylic cement into the vertebral bodies only after pedicle screws implementation. MATERIALS AND METHODS: For the purpose of conducting this research, the authors used the spines of fully-grown pigs. The procedure was as follows: firstly, the pedicle screws were bilaterally implemented in 10 vertebrae; secondly, cancellous bone was removed from vertebral bodies selected for screws augmentation and lastly it was replaced by polymethylmethacrylate (PMMA). Six vertebrae with implemented pedicle screws served as a control group. The pullout strength of thirty-two screws (20 augmented and 12 control) was tested. All screws were pulled out at a crosshead speed of 5mm/min. RESULTS: The PMMA-augmented screws showed a 1.3 times higher average pullout force than the control group: respectively 1539.68N and 1156.59N. In essence, no significant discrepancy was determined between average pullout forces of screws which were pulled as first when compared with consecutive contralateral ones. CONCLUSIONS: An in vitro simulation of intraoperative injection of PMMA in the vertebral body instrumented with screws (intraoperative vertebroplasty) resulted in enhancing its pullout strength by 33%. Pulling of one of the pedicular screws from the augmented vertebral body did not affect the pullout resistance of the contralateral one.

Multishelled CaO Microspheres Stabilized by Atomic Layer Deposition of Al2 O3 for Enhanced CO2 Capture Performance.

CO2 capture and storage is a promising concept to reduce anthropogenic CO2 emissions. The most established technology for capturing CO2 relies on amine scrubbing that is, however, associated with high costs. Technoeconomic studies show that using CaO as a high-temperature CO2 sorbent can significantly reduce the costs of CO2 capture. A serious disadvantage of CaO derived from earth-abundant precursors, e.g., limestone, is the rapid, sintering-induced decay of its cyclic CO2 uptake. Here, a template-assisted hydrothermal approach to develop CaO-based sorbents exhibiting a very high and cyclically stable CO2 uptake is exploited. The morphological characteristics of these sorbents, i.e., a porous shell comprised of CaO nanoparticles coated by a thin layer of Al2 O3 (<3 nm) containing a central void, ensure (i) minimal diffusion limitations, (ii) space to accompany the substantial volumetric changes during CO2 capture and release, and (iii) a minimal quantity of Al2 O3 for structural stabilization, thus maximizing the fraction of CO2 -capture-active CaO.

Development of a Steel-Slag-Based, Iron-Functionalized Sorbent for an Autothermal Carbon Dioxide Capture Process.

We propose a new class of autothermal CO2 -capture process that relies on the integration of chemical looping combustion (CLC) into calcium looping (CaL). In the new process, the heat released during the oxidation of a reduced metallic oxide is utilized to drive the endothermic calcination of CaCO3 (the regeneration step in CaL). Such a process is potentially very attractive (both economically and technically) as it can be applied to a variety of oxygen carriers and CaO is not in direct contact with coal (and the impurities associated with it) in the calciner (regeneration step). To demonstrate the practical feasibility of the process, we developed a low-cost, steel-slag-based, Fe-functionalized CO2 sorbent. Using this material, we confirm experimentally the feasibility to heat-integrate CaCO3 calcination with a Fe(II)/Fe(III) redox cycle (with regards to the heat of reaction and kinetics). The autothermal calcination of CaCO3 could be achieved for a material that contained a Ca/Fe ratio of 5:4. The uniform distribution of Ca and Fe in a solid matrix provides excellent heat transfer characteristics. The cyclic CO2 uptake and redox stability of the material is good, but there is room for further improvement.

CaO-based CO2 sorbents: from fundamentals to the development of new, highly effective materials.

The enormous anthropogenic emission of the greenhouse gas CO2 is most likely the main reason for climate change. Considering the continuing and indeed growing utilisation of fossil fuels for electricity generation and transportation purposes, development and implementation of processes that avoid the associated emissions of CO2 are urgently needed. CO2 capture and storage, commonly termed CCS, would be a possible mid-term solution to reduce the emissions of CO2 into the atmosphere. However, the costs associated with the currently available CO2 capture technology, that is, amine scrubbing, are prohibitively high, thus making the development of new CO2 sorbents a highly important research challenge. Indeed, CaO, readily obtained through the calcination of naturally occurring limestone, has been proposed as an alternative CO2 sorbent that could substantially reduce the costs of CO2 capture. However, one of the major drawbacks of using CaO derived from natural sources is its rapidly decreasing CO2 uptake capacity with repeated carbonation-calcination reactions. Here, we review the current understanding of fundamental aspects of the cyclic carbonation-calcination reactions of CaO such as its reversibility and kinetics. Subsequently, recent attempts to develop synthetic, CaO-based sorbents that possess high and cyclically stable CO2 uptakes are presented.

High-purity hydrogen via the sorption-enhanced steam methane reforming reaction over a synthetic CaO-based sorbent and a Ni catalyst.

Sorbent-enhanced steam methane reforming (SE-SMR) is an emerging technology for the production of high-purity hydrogen from hydrocarbons with in situ CO2 capture. Here, SE-SMR was studied using a mixture containing a Ni-hydrotalcite-derived catalyst and a synthetic, Ca-based, calcium aluminate supported CO2 sorbent. The fresh and cycled materials were characterized using N2 physisorption, X-ray diffraction, and scanning and transmission electron microscopy. The combination of a Ni-hydrotalcite catalyst and the synthetic CO2 sorbent produced a stream of high-purity hydrogen, that is, 99 vol % (H2O- and N2-free basis). The CaO conversion of the synthetic CO2 sorbent was 0.58 mol CO2/mol CaO after 10 cycles, which was more than double the value achieved by limestone. The favorable CO2 capture characteristics of the synthetic CO2 sorbent were attributed to the uniform dispersion of CaO on a stable nanosized mayenite framework, thus retarding thermal sintering of the material. On the other hand, the cycled limestone lost its nanostructured morphology completely over 10 SE-SMR cycles due to its intrinsic lack of a support component.

Influence of the calcination and carbonation conditions on the CO2 uptake of synthetic Ca-based CO2 sorbents.

In this work we report the development of a Ca-based, Al(2)O(3)-stabilized sorbent using a sol-gel technique. The CO(2) uptake of the synthetic materials as a function of carbonation and calcination temperature and CO(2) partial pressure was critically assessed. In addition, performing the carbonation and calcination reactions in a gas-fluidized bed allowed the attrition characteristics of the new material to be investigated. After 30 cycles of calcination and carbonation conducted in a fluidized bed, the CO(2) uptake of the best sorbent was 0.31 g CO(2)/g sorbent, which is 60% higher than that measured for Rheinkalk limestone. A detailed characterization of the morphology of the sol-gel derived material confirmed that the nanostructure of the synthetic material is responsible for its high, cyclic CO(2) uptake. The sol-gel method ensured that Ca(2+) and Al(3+) were homogenously mixed (mostly in the form of the mixed oxide mayenite). The formation of a finely and homogeneously dispersed, high Tammann temperature support stabilized the nanostructured morphology over multiple reaction cycles, whereas limestone lost its initial nanostructured morphology rapidly due to its intrinsic lack of a support component.

Coprecipitated, copper-based, alumina-stabilized materials for carbon dioxide capture by chemical looping combustion.

Chemical looping combustion (CLC) has emerged as a carbon dioxide capture and storage (CCS) process to produce a pure stream of CO(2) at very low costs when compared with alternative CCS technologies, such as scrubbing with amines. From a thermodynamic point of view, copper oxide is arguably the most promising candidate for the oxygen carrier owing to its exothermic reduction and oxidation reactions and high oxygen-carrying capacity. However, the low melting point of pure copper of only 1085 °C has so far prohibited the synthesis of copper-rich oxygen carriers. This paper is concerned with the development of copper-based and Al(2)O(3)-stabilized oxygen carriers that contain a high mass fraction of CuO, namely, 82.4 wt %. The oxygen carriers were synthesized by using a coprecipitation technique. The synthesized oxygen carriers were characterized in detail with regards to their morphological properties, chemical composition, and surface topography. It was found that both the precipitating agent and the pH at which the precipitation was performed strongly influenced the structure and chemical composition of the oxygen carriers. In addition, XRD analysis confirmed that, for the majority of the precipitation conditions investigated, CuO reacted with Al(2)O(3) to form fully reducible CuAl(2)O(4). The redox characteristics of the synthesized materials were evaluated at 800 °C by using methane as the fuel and air for reoxidation. It was found that the oxygen-carrying capacity of the synthesized oxygen carriers was strongly influenced by both the precipitating agent and the pH at which the precipitation was performed; however, all oxygen carriers tested showed a stable cyclic oxygen-carrying capacity. The oxygen carriers synthesized at pH 5.5 using NaOH or Na(2)CO(3) as the precipitating agents were the best oxygen carriers synthesized owing to their high and stable oxygen transfer and uncoupling capacities. The excellent redox characteristics of the best oxygen carrier were interpreted in light of the detailed morphological characterization of the synthesized material and a synthesis-structure-performance relationship was developed.