Na2CO3 Aqueous Solution Research Articles

Fabrication of NiO/TiO2/rGO nanocomposites as a quasi-solid-state asymmetric supercapacitor: Paving the way for PhotoSupercapacitor application

In this present communication, a novel ternary nanocomposite, NiO/TiO2/rGO (NTG), was synthesised via a simple hydrothermal technique for photosupercapacitor application. The XRD pattern confirmed the crystalline nature and phase structure of the as-synthesised material. FE-SEM and HR-TEM analyses demonstrated the embellishment of NiO/TiO2 nanoparticles on the rGO sheets, which facilitates more voids and shorter diffusion paths. The electrochemical investigation of the prepared samples was assessed using 1 M Na2SO4 and Na2CO3 aqueous electrolyte solutions. Among the synthesised samples, NTG-2 carried out under 1 M Na2SO4 electrolyte exhibited a maximum specific capacitance of 1285 Fg-1 at 1 Ag-1, maintaining a capacitance retention of 94 % after 5000 cycles. The NTG-2 electrode was additionally utilised in the construction of an asymmetric supercapacitor that has an impressive specific capacitance of 478 Fg-1 at 1 Ag-1. This displays an intriguing performance in terms of energy and power density of 42.2 Wh Kg−1 at 0.5 kW kg−1. In PSC, the as-fabricated TiO2/N719/I−/I3−/Pt@NTG-2//AC architecture possessed a specific capacitance of 567.5 Fg-1 at 1 Ag-1, with an energy density of 50.4 Wh Kg−1 and a power density of 0.4 kW kg−1. As a result, it has been concluded that the novel NTG-2 device opens new opportunities to develop new architectures for efficient energy storage applications.

Size Control of Biomimetic Curved-Edge Vaterite with Chiral Toroid Morphology via Sonochemical Synthesis.

The metastable vaterite polymorph of calcium carbonate (CaCO3) holds significant practical importance, particularly in regenerative medicine, drug delivery, and various personal care products. Controlling the size and morphology of vaterite particles is crucial for biomedical applications. This study explored the synergistic effect of ultrasonic (US) irradiation and acidic amino acids on CaCO3 synthesis, specifically the size, dispersity, and crystallographic phase of curved-edge vaterite with chiral toroids (chiral-curved vaterite). We employed 40 kHz US irradiation and introduced L- or D-aspartic acid as an additive for the formation of spheroidal chiral-curved vaterite in an aqueous solution of CaCl2 and Na2CO3 at 20 ± 1 °C. Chiral-curved vaterites precipitated through mechanical stirring (without US irradiation) exhibited a particle size of approximately 15 μm, whereas those formed under US irradiation were approximately 6 μm in size and retained their chiral topoid morphology. When a fluorescent dye was used for the analysis of loading efficiency, the size-reduced vaterites with chiral morphology, produced through US irradiation, exhibited a larger loading efficiency than the vaterites produced without US irradiation. These results hold significant value for the preparation of biomimetic chiral-curved CaCO3, specifically size-reduced vaterites, as versatile biomaterials for material filling, drug delivery, and bone regeneration.

Potential of hardwood kraft lignin as a bio-based dye for cotton fabrics

The dyeing characteristics of hardwood kraft lignin (KL) were investigated on cotton fabrics, assessing its potential as a sustainable and environmentally friendly dye. Dyeability was evaluated by varying the KL concentrations, temperature, and time. An aqueous solution of Na2CO3 (1.0%) as the dye bath and a fabric-to-liquor ratio of 1:50 were used. Cationizing effects were studied using (3-chloro-2-hydroxypropyl) trimethylammonium chloride (CHPTAC), and the mordanting effects of various mordants were also evaluated. Post-mordanting was performed with FeSO4, FeCl2, Fe-lactate (Fe-lac), MgSO4, CuCl2, CuSO4, and Al2(SO4)3. A mordant concentration of 1 mM o.w.f. (0.5 mM for Al2(SO4)3), with a liquor ratio of 1:30, at 60 °C for 30 min were employed. Suitable dyeing conditions were 2.0% o.w.b., 90 °C, and 90 min, resulting in a brownish color of the cotton fabric. The fabrics exhibited a range of light brown to light grayish brown colors and showed lighter colors than the untreated fabrics when mordanted with MgSO4 and Al2(SO4)3. The color difference (ΔE) between cationized and uncationized cotton fabrics was 3.48. From the colorfastness assessment, KL-dyed cotton fabric showed good rubbing and washing fastness for staining, but poor light and washing fastness for fading.

Assembling of a Water-Soluble N^C^N-Coordinated Pt(II) Complex Aggregate Assisted by Carbon Dioxide in Basic Aqueous Solution.

We report an unprecedented result of self-aggregation of [Pt(L1 )Cl] (HL1 =1,3-di(5-carboxy-2-pyridyl)benzene) triggered by CO2 in basic aqueous solution. The color of basic aqueous solution containing [Pt(L1 )Cl] changes from yellow to blue-green during the aggregation resulted from a reaction with CO2 in air. Upon CO2 gas bubbling, strong and broad absorption bands of aggregate assigned to the metal-metal-to-ligand charge-transfer transition appeared at 701 and 1152 nm. Recrystallization of [Pt(L1 )Cl] from Na2 CO3 aqueous solution afforded polymorphic crystals of red and blue-green forms. A single X-ray crystallography revealed that the red form of crystal consists of a Pt-Pt stacked dimer bridged by CO3 2- ion and one of the carboxy groups of L1 is deprotonated. An elemental analysis provided evidence that the blue-green crystal is constructed by linear array consisting of the [Pt(L2 )(CO3 )]3- (HL2 =1,3-di(5-carboxylate-2-pyridyl)benzene) units. The formation process of blue-green aggregate in aqueous solution was monitored through a transient absorption spectrum, and the absorption of aggregates involved in the spectral change were examined by a global analysis. A singular value decomposition and kinetic analysis provide that there are four species resulted from the self-assembling reaction in the solution and the maximal degree of aggregation is at least 32-mer.

Aluminium extraction from a calcium aluminate slag using sodium carbonate based on the critical examination of the patented industrial Pedersen process

The extraction of aluminium from calcium aluminate phases by leaching with Na2CO3 solutions has been researched intermittently for more than a hundred years. In the 21st century, this process has gained a renewed interest for the design of novel metallurgical methods. The Pedersen Process has been the only known successful industrial scale application of calcium aluminate leaching to date. The engineering principles that ensured plant operations remained, until recently, unknown. These principles are critically assessed for the first time, based on recently retrieved patents submitted at the time the Pedersen process was in operation. The findings of the previous analysis were used for an experimental study with the two goals: (i) to validate the principles applied in the industrial Pedersen process and (ii) to apply these principles in designing an optimized leaching process for calcium aluminate slags originating from alternative Al sources. The calcium aluminate slag used in this study is the by-product of an aluminothermic reduction process for Si production along with an 8% (w/w) Na2CO3 aqueous solution. Results confirmed the majority of the assumed principles. All the tested leaching conditions produced Al extraction in the range of 75% - 95% (w/w).

Characterization of alginate from Antarctic Himantothallus grandifolius (Phaeophyceae) and preparation of polyelectrolyte complexes with chitosan

AbstractHydrogels are three‐dimensional polymeric materials with applications in various areas such as biomedicine, tissue engineering, pollutant capture systems, and so forth. However, its application is limited due to the reproducibility of its properties. Factors such as the composition of the constituents, the type of union between the polymer chains, and the crosslinking time play a crucial role in ensuring its reproducibility. In this study, the objective is to prepare a matrix with well‐defined properties that ensure controlled release processes. Treatment of Himantothallus grandifolius with Na2CO3 aqueous solution afforded in 18.9% yield alkaline extract. Hydrogels were prepared by ionic complexation of alginate from H. grandifolius, and polyguluronate enriched alginate from Desmarestia ligulata with chitosan stabilized by immersion in 0.1 M CaCl2 solution; better swelling ratio in water was found for hydrogels with low molecular weight chitosan (MW 125,000 g/mol) than those with medium molecular weight chitosan (MW450,000–500,000 g/mol). Liberation of the model drug metformin hydrochloride from alginates: chitosan complexes (3:1) at pH 1.5 was especially low for hydrogel from H. grandifolius during the first 2 h; 70% of metformin was released at pH 6.5 after 24 h. This polyelectrolyte complex constitutes a good material for potential application in biomedicine considering its cationic and anionic characteristics.

A facile method to fabricate multifunctional polyvinyl alcohol mineralized hydrogels with high strength and adaptable shape

AbstractHydrogel‐based materials are widely used in many fields, but most of them compared to tendons with the same water content do not exhibit high toughness, strength or fatigue resistance, which limits their application. The Hofmeister effect can adjust the mechanical properties of hydrogels by ions affecting the aggregation of polymer chains. Herein, we prepared a bioactivated hydrogel through simply mixing polyvinyl alcohol (PVA) and Na2CO3 aqueous solutions. PVA chains are aggregated by strong hydrogen bonds between CO32− and OH, at which stage the hydrogel is soft and easy to shape. Further salting out promotes the formation of crystal microphase of PVA chain, resulting in high mechanical strength and excellent toughness. The existence of Na2CO3 endow the hydrogel with conductivity, exhibits high and stable sensitivity in strain sensing, and could be used to monitor human actions. On the basis of this method, Ca2+ was added to prepare mineralized PVA hydrogels, which had high stability and long‐term swelling resistance in different ionic solutions. In vitro cell experiment, hydrogel had obvious effect of promoting bone cell proliferation and calcium deposition. This work provides a facile and feasible method for preparing bionic hydrogels with high strength, toughness, and adaptable shape.

SPECTRAL AND PHOTOPHYSICAL CHARACTERISTICS OF ASYMMETRIC POLYMETHINE DYES IN POLYURETHANE MATRICES

Here the composite polymer sorbent hydrogels were synthesized by in situ technique via free radical polymerization of acrylamide (AAm), 2-hydroxyethyl methacrylate (2HEMA) and N,N’-methylene-bis(acrylamide) crosslinker mixture in the presence of as-prepared dispersion of nickel-aluminum layered double hydroxide (NiAl-LDH). A content of active NiAl-LDH filler in the polymer matrix was varied in a range of 30 – 70 wt.%. It was found a high filler content suppresses a molecular mobility of copolymer matrix chains and reduces a beginning of glass transition temperature of the polymer constituent. The results of thermal analysis of polymer composites demonstrate a high hydrophilicity level of polymer matrix and high solvation energy of polar functionalities by Н2О molecules that was concluded from slow moisture elimination process while the temperature grows up to 200–210 оС. Additionally, a dehydration process and changes in a structure of thermally labile filler were also observed at the same temperature interval. At higher temperatures a thermal degradation of polymer poly(AAm-co-2HEMA) matrix is carried out. When a temperature overcomes 400 оС the partially changed filler demonstrates a chemical interaction with degraded organic constituents of the composites and defined catalytic activity as well. Studying sorption activity of the composites shown that introducing NiAl-LDH into hydrophilic polymer matrix provides anion-exchange activity to the composite sorbents and, correspondingly, the ability to eliminate the anionic contaminants from aqueous media while the polymer matrix doesn’t absorb these substances at such conditions. The highest sorption capacity of 11,40 μmol/g against model contaminant – methyl orange dye was determined for composite sorbent with filler content of 70 wt. %. At the same time sorption capacity of NiAl-LDH filler in composite sorbents reduces from 25,7 to 16,6 μmol/g while a filler content grows from 30 to 70 wt.% as a result of filler particles aggregation processes during composites formation stage. To evaluate the ability of the composite sorbents to reuse the experiment of materials recycling was performed. It was stated out the using of anion-exchange technique and aqueous Na2CO3 solution as an efficient and non-hazardous eluent provides 80 % recovering efficiency of the active filler in the composites. It can be concluded the composite sorbents demonstrate a high overall efficiency and are valuable materials for practical application for decontamination of waste water.

A Modified Folin-Ciocalteu Assay for the Determination of Total Phenolics Content in Honey

The Folin-Ciocalteu assay is a widely used method for measuring the total phenolic content (TPC) in honey, but it can be affected by the presence of reducing sugars in honey, which can lead to interference and an over-estimation of its TPC. To optimize the Folin-Ciocalteu assay for honey analysis, the effect of pH on the assay was investigated. A number of pH scenarios were tested using different concentrations of Na2CO3 (0.00%, 0.75%, 0.94%, and 7.50%) in order to minimize reducing sugar interference and maximize the reaction of phenolics in the assay. The modified TPC method was then validated in accordance with current International Council on Harmonisation (ICH) guidelines. The findings of this study demonstrate that the traditional Folin-Ciocalteu assay (using 7.50% aqueous Na2CO3 solution, pH 10.8) leads to a significant overestimation of the TPC of honey due to the interference of reducing sugars. However, a pH of 7.9, achieved by using a 0.75% aqueous Na2CO3 solution, provides suitable conditions to account for most of the phenolic compounds without interference from reducing sugars. This finding was further confirmed by testing various sugar solutions and artificial honey which yielded TPC values below the established limit of detection and quantification of the assay. However, a slight increase in pH, even by a moderate deviation (pH 8.9), leads to significant discrepancies in absorbance readings, indicating that pH control is crucial for the accurate analysis of TPC in honey.

Energy Balance of Hydrogen Production in the Cathodic Regime of Plasma-Driven Solution Electrolysis of Na2CO3 Aqueous Solution with Argon Carrier Gas

In this paper, the results of an experimental study on hydrogen production at a tungsten discharge electrode with negative polarity in the DC electrolysis of a typical 10 wt% Na2CO3 aqueous solution in three operational regimes (the Faradaic, transition, and plasma-driven solution electrolysis (PDSE)) are presented for the first time. To focus the study on hydrogen production, a flowing inert gas (argon) was used to transport the gas mixture produced at the discharge electrode and prevent any other potential chemical reactions. The results showed that the highest hydrogen production rate of 0.147 g(H2)/h was achieved in the cathodic PDSE regime at the applied DC voltage of 198 V. However, the energy yield of hydrogen production of 0.405 g(H2)/kWh obtained at the applied voltage range of 141–170 V in the PDSE regime was lower than that obtained in the Faradaic regime (0.867 g(H2)/kWh) at 28 V. The energy balance of hydrogen production in the cathodic PDSE regime for the typical aqueous solution of Na2CO3 carried out for the first time showed that a significant share (˃98%) of the electrical energy consumed is spent on heating and evaporation of the electrolytic solution. This explains why the energy yield of hydrogen production is low in the PDSE regime. Because most of the energy is consumed for heat generation in the cathodic PDSE regime, organic liquid hydrogen carriers, such as alcohols, which have a lower boiling temperature, heat of evaporation, and standard Gibbs free energy, should be considered better aqueous electrolytic solutions in terms of the energy yield of hydrogen production in the PDSE regime.

Hydrogen-bond mediated and concentrate-dependent NaHCO3 crystal morphology in NaHCO3–Na2CO3 aqueous solution: Experiments and computer simulations

Adding Na2CO3 to the NaHCO3 cooling crystallizer, using the common ion effect to promote crystallization and improve product morphology, is a new process recently proposed in the literature. However, the mechanism of the impact of Na2CO3 on the crystal morphology is still indeterminate. In this work, the crystallization of NaHCO3 in water and Na2CO3–NaHCO3 aqueous solution was investigated by experiments and molecular dynamics simulations (MD). The crystallization results demonstrate that the morphology of NaHCO3 crystal changed gradually from needle-like to flake structure with the addition of Na2CO3. The simulation results indicate that the layer docking model and the modified attachment energy formula without considering the roughness of crystal surface can obtain the crystal morphology in agreement with the experimental results, but the lower molecules of the crystal layer have to be fixed during MD. Thermodynamic calculation of the NaHCO3 crystallization process verifies that the common ion effect from Na+ and the ionization equilibrium transformation from CO32– jointly promote the precipitation of NaHCO3 crystal. The radial distribution function analysis indicates that the oxygen atoms of Na2CO3 formed strong hydrogen bonds with the hydrogen atoms of the (0 1 1) face, which weakened the hydration of water molecules at the crystal surface, resulting in a significant change in the attachment energy of this crystal surface. In addition, Na+ and CO32– are more likely to accumulate on the (0 1 1) face, resulting in the fastest growth rate on this crystal surface, which eventually leads to a change in crystal morphology from needle-like to flake-like.

Equilibrium thickness of foam films and adsorption of ions at surfaces: Aqueous solutions of sodium hydrogencarbonate and sodium carbonate

Hypothesis.The origin of the negative charge at water/air interface was proved to be not only specific adsorption of OH– ions but that of HCO3– and/or CO32– ions in the previous study [1]. To determine which anionic species is primarily responsible for the surface charge, the surface density of ions in the Stern layer is numerically evaluated from foam-film thickness of aqueous solutions of NaHCO3 and Na2CO3.Experiments.Equilibrium thickness (equivalent thickness at equilibrium) of the foam films formed from aqueous solutions of NaHCO3 and Na2CO3 was measured as a function of electrolyte concentration at 298.15 K.Findings.Applying a modified Poisson-Boltzmann (PB) equation developed for various kinds of electrolytes to the equilibrium thickness gave the surface density of ions in the Stern layer for NaHCO3 and Na2CO3 systems. From the concentration dependence of the surface density together with that for NaCl and NaOH in the previous study [1], the negative surface charges for water and very dilute solutions were found to be due to specific adsorption of HCO3– ions. The surface charge at high electrolyte concentration is determined by the specific adsorption of electrolyte anions. The specific-adsorption ability of anion increases in the order CO32–≫ HCO3–> OH–≫ Cl-.

Rehydration Driven Na-Activation of Bentonite-Evolution of the Clay Structure and Composition.

A new method of Na-activation of raw bentonite, rich in Ca-montmorillonite, consisting of combined thermal treatment at 200 °C, followed by immediate impregnation with aqueous solution of Na2CO3 of concentration corresponding to 0.5, 1.0, 1.5, or 2.0 cation exchange capacity (CEC) of clay, was investigated. Structural and compositional evolution of the activated solids after 1, 2, 3, and 4 weeks of storage was monitored by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). XRD analysis indicated that within the investigated period of ageing transformation to Na-rich montmorillonite required Na2CO3 concentration of at least 1.0 CEC. FTIR spectra showed that, depending on the Na2CO3 concentration and ageing time, formation of Na-rich montmorillonite was accompanied by precipitation of poorly crystalline calcite, amorphous calcium carbonate, gaylussite (a double calcium-sodium carbonate), and portlandite (Ca(OH)2).

Efficient production of biodiesel with electric furnace dust impregnated in Na2CO3 solution

Solid catalyst (Na2CO3@EFD) was prepared by wet impregnation of electric furnace dust (EFD) in aqueous Na2CO3 solution. It had high basicity and acidity of 0.34 and 0.16 mmol/g for biodiesel production. High biodiesel yield of 99.8 wt% from soybean oil was obtained under the optimized reaction conditions (by Central Composite Design) of 71 °C in 111.36 min with 5.4 wt% catalyst and methanol/oil molar ratio of 11.8/1. After 11 cycles, biodiesel yield still maintained at 90.8 wt% with catalyst recovery rate >90 wt% by magnetic separation of catalyst EFD powders (containing Fe3O4 with magnetism of 59.1 Am2/kg). Pure Na2CO3 particles presented poorer recyclability with lower biodiesel yield of 89.5 wt% even at the eighth cycle by centrifugal separation. Na2CO3@EFD catalyst had high activity and recyclability because: (i) EFD as support hosted nanoparticles of Na2CO3 (30.3 nm) as main base site for transesterification; (ii) porous EFD support provided acidic sites from metal oxides (e.g., ZnO and Al2O3) for esterification; (iii) EFD adsorbed active components into its micropores to maintain high recyclability; and (iv) EFD magnetism from magnetic Fe3O4 kept high efficient magnetic separation. Total metals in the blended biodiesel met the National Standard of China and heavy metals were lower than typical petrochemical diesel. The study gave a practical use of industrial solid waste for the green production of biodiesel.

Self-Healing Hydrophilic Porous Photothermal Membranes for Durable and Highly Efficient Solar-Driven Interfacial Water Evaporation

Self-Healing Hydrophilic Porous Photothermal Membranes for Durable and Highly Efficient Solar-Driven Interfacial Water Evaporation

Leaching of Ca-Rich Slags Produced from Reductive Smelting of Bauxite Residue with Na2CO3 Solutions for Alumina Extraction: Lab and Pilot Scale Experiments

Sustainable utilization of Bauxite Residue (BR) is currently one of the greatest challenges being tackled by the alumina industry, due to its high production rates and limited reuse options. The present work is concerned with the use of BR as a candidate metallurgical raw material for iron (Fe) production and aluminum (Al) extraction. In more detail, at first, BR undergoes reductive smelting to extract its Fe content and produce a slag of mainly calcium aluminate composition. In a second step, Al contained in the calcium aluminate phases is extracted hydrometallurgically by leaching with a Na2CO3 aqueous solution. The focus of the current study is the optimization of this leaching process, and it was performed in two stages. The first was a laboratory scale investigation on the main parameters affecting the extraction rate of Al. The second stage was performed in pilot scale and incorporated observations and suggestions based on the laboratory scale investigation. Laboratory work showed that more than 50% of aluminum could be easily extracted in less than 1 h, in 5% S/L, at 70 °C and with an 20% excess of Na2CO3. Pilot scale work, by successfully applying the suggestions derived from laboratory scale work, achieved an average Al extraction of 68% from a 10% S/L pulp, with a slag of optimized composition in relation to the one used in the laboratory scale.

Separation of uranium(VI) and americium(III) by Extraction from Na2CO3–H2O2 solutions using methyltrioctylammonium carbonate in toluene

ABSTRACT Liquid–liquid extraction of carbonate and mixed peroxo-carbonate compounds of U(VI) and Am(III) from Na2CO3 aqueous solutions by methyltrioctylammonium carbonate in toluene has been studied. The main patterns of effect of extractant, Na2CO3, and H2O2 concentration on distribution and separation of U(VI) and Am(III) have been established. Using slope analysis and UV–vis spectroscopy, the compositions of U(VI) and Am(III) extractable compounds are established as (R4N)4[UO2(CO3)3], (R4N)4[UO2(О2)(CO3)2], and (R4N)6[(UO2)2(O2)(CO3)4] for U(VI); R4N[Am(CO3)2] and (R4N)3[Am(CO3)3] for Am(III), where R4N is the quaternary ammonium cation. The obtained data showed high efficiency of the studied carbonate system for extraction of U(VI) and its purification from Am(III). The maximum separation factor of U(VI) and Am(III) was 25.

DBU Catalysed Enantioselective Degradative Rearrangement: a Way to Tetrasubstituted 2‐Aryl‐2‐Amino Esters

AbstractHerein we report a catalytic, easily scalable protocol for the enantioselective synthesis of Tetrasubstituted α‐aryl‐α‐amino acid derivatives, using a biphasic system composed by catalytic DBU in DME and aqueous solutions of Na2CO3. Under very mild reaction conditions, without using metal or chiral additives, this heterogeneous system promotes the degradative rearrangement of functionalized N‐aryl sulphonyl α‐amino esters into the corresponding tetrasubstituted 2‐aryl‐2‐amino esters, with high enantiomeric ratios (up to 97.5:2.5) and good yields (up to 95%).magnified image

Cross-Linked and Functionalized Acrylic Polymers: Efficient and Reusable Sorbents for Zn(II) Ions in Solution

The efficiency of the three types of cross-linked and functionalized with triethylenetetramine (As30 and As32) and acylate diethylenediamine (Cm26) acrylic polymers towards zinc ions from synthetic wastewaters has been investigated under different experimental conditions. The sorption and reusability of metal ions on three types of polymer were studied by the static and dynamic method. The effects of contact time, the initial metal ion concentration, pH, sorbent mass and temperature on the adsorption capacity of the three types of cross-linked and functionalized acrylic polymers were investigated. The thermodynamic parameters associated with the adsorption process were evaluated, and obtained values suggested an exothermic process. The experimental data confirm much better to the Langmuir isotherm than the Freundlich, Temkin, Dubinin–Radushkevich, Sips and Flory–Huggins isotherms. The obtained values for the separation factor, RL were less than 1 one which shows that the adsorption process was favorable. The obtained results indicated that the Cm26 has a higher sorption capacity (1135.77 43 mg g−1) towards zinc ions than As32 (1059.47 43 mg g−1) and As 30 (857.77 43 mg g−1) at 293 K. The adsorption capacity sorbents towards Zn2+ ions after five consecutive sorption/desorption cycles, with 0.1 M Na2CO3 aqueous solution as eluent, decreased with about 5% of the initial sorption capacity and this fact recommended the potential of these functionalized polymers in the removal of Zn(II) ions from residual waters.

The effects of power ultrasound (24 kHz) on the electrochemical reduction of CO2 on polycrystalline copper electrodes

The electrochemical CO2 reduction reaction (CO2RR) on polycrystalline copper (Cu) electrode was performed in a CO2-saturated 0.10 M Na2CO3 aqueous solution at 278 K in the absence and presence of low-frequency high-power ultrasound (f = 24 kHz, PT ~ 1.23 kW/dm3) in a specially and well-characterized sonoelectrochemical reactor. It was found that in the presence of ultrasound, the cathodic current (Ic) for CO2 reduction increased significantly when compared to that in the absence of ultrasound (silent conditions). It was observed that ultrasound increased the faradaic efficiency of carbon monoxide (CO), methane (CH4) and ethylene (C2H4) formation and decreased the faradaic efficiency of molecular hydrogen (H2). Under ultrasonication, a ca. 40% increase in faradaic efficiency was obtained for methane formation through the CO2RR. In addition, and interestingly, water-soluble CO2 reduction products such as formic acid and ethanol were found under ultrasonic conditions whereas under silent conditions, these expected electrochemical CO2RR products were absent. It was also found that power ultrasound increases the formation of smaller hydrocarbons through the CO2RR and may initiate new chemical reaction pathways through the sonolytic di-hydrogen splitting yielding other products, and simultaneously reducing the overall molecular hydrogen gas formation.