A green extraction technology of lignocellulose from cassava residue by mechanical activation-assisted ternary deep eutectic solvent.

Lignocellulose (LC) is a natural polymer material that holds immense potential for various applications. However, extracting LC from biomass wastes with high-starch content has been challenging due to low selectivity and yield. In this study, LC was prepared from cassava residue (CR) via a combination of mechanical activation pretreatment and a citric acid (CA)-enhanced ternary deep eutectic solvent (TDES) consisting of choline chloride (ChCl), lactic acid (LA), and CA. The mechanical activation reduces the size of CR, greatly promoting the removal ability for starch, lignin and hemicellulose using TDES, and thus improving yield and selectivity of LC through this method. The CA esterified LC to prevent its excessive hydrolysis and increased a significantly higher LC content (82.52 wt%) compared to mechanical activation only and DES without CA, increasing by 6.97 times and 1.26 times, respectively. The extraction temperature significantly affected the structure, composition, thermal stability of LC and the properties of recovered TDES. The LC extracted at 90 °C (LC-90) had the highest cellulose content (82.52 wt%), crystallinity index (44.82 %), and higher degradation temperature (339.7 °C). The properties of the recovered TDES and extraction mechanism were analyzed. This study provides a strategy for the high-value utilization of biomass waste.

Bi-functional NiFe2O4/SrTiO3 S-scheme heterojunction for eminent performance photocatalytic treatment of sewage effluent and electrochemical hydrazine determination.

Devising of materials that afforded dual applicability in decontamination and pollutant detection were still a towering challenge owing to the increasing flux of discharge toxic contaminants over the years. Herein, the NiFe2O4 nanoparticles-loaded on cube-like SrTiO3 (NiFe2O4/SrTiO3) composite was fabricated by a two-step hydrothermal approach providing remarkable photocatalytic treatment and electrochemical sensing of noxious pollutants in wastewater. The material traits of the fabricated composite were scrutinized by myriad characterization approaches. The NiFe2O4/SrTiO3 hybrid material demonstrated high surface area of 19.81 m2/g, adequate band gap energy of 2.75 eV, and prominent photoluminescence characteristics. In the presence of visible light, the NiFe2O4/SrTiO3 exhibited profound photocatalysis capability to eliminate sewage effluent-bearing chlortetracycline hydrochloride (CTCH) with 88.6% COD removal in 120 min, outperforming other pure materials. Meanwhile, the toxicity examination of effluent, the possible degradation pathway of CTCH and the proposed photocatalysis mechanism were also divulged. More importantly, the glassy carbon electrode was modified with synergized NiFe2O4/SrTiO3 (NiFe2O4/SrTiO3-GCE) was adopted for the precise quantification of Hydrazine (Hz). The NiFe2O4/SrTiO3-GCE obeyed first-order response for the Hz detection within the range of 1-10 mM: cyclic voltametric: limit of detection (LOD) of 0.119 µM with sensitivity of 18.9 µA µM-1 cm-2, and linear sweep voltametric: LOD of 0.222 µM with a sensitivity of 12.05 µA µM-1 cm-2. The stability and interference of modified electrode were also inspected. This work furnished valuable insights to yield a composite with the prominent S-scheme heterojunction system for quenching of charge carrier recombination and consequently contributing to the future realization into the domains of environmental clean-up and toxic chemical detection.

Highly Stable Ni-B/Honeycomb-Structural Al2O3 Catalysts for Dry Reforming of Methane.

Two-component catalysts have garnered significant attention in the field of catalysis due to their ability to inhibit Ni sintering. In the present work, honeycomb-structuralstructured Al2O3-supported Ni and B were prepared to enhance coke tolerance during dry reforming of methane (DRM). Transmission electron microscopy (TEM) results revealed that the average particle sizes on Ni/Al2O3 and Ni-0.16B/Al2O3 were 7.6 nm and 4.2 nm, respectively, indicating that B can effectively inhibit Ni sintering. After a 100-hour reaction, the conversion of CH4 and CO2 on Ni/Al2O3 decreased by approximately 5 %, whereas on Ni-0.16B/Al2O3, there was no significant decrease in CH4 and CO2 conversion, with values of approximately 81.6 % and 87.2 %, respectively. In situ DRIFT spectra demonstrated that Ni-0.16B/Al2O3 enhanced the activation of CO2, thus improving the catalyst's stability. A Langmuir-Hinshelwood-Hougen-Watson (LHHW) model was developed for intrinsic kinetics, and the resulting kinetic expressions were well-fitted fit to the experimental data, with R2 values exceeding 0.9. ActivationThe activation energies were also calculated. The outstanding stability of Ni-0.16B/Al2O3 can be attributed to its stable honeycomb structure and B's ability to significantly inhibit Ni sintering, reduce catalyst particle size, and enhance coke tolerance.

WO3/BiOBr S-Scheme Heterojunction Photocatalyst for Enhanced Photocatalytic CO2 Reduction.

The photocatalytic CO2 reduction strategy driven by visible light is a practical way to solve the energy crisis. However, limited by the fast recombination of photogenerated electrons and holes in photocatalysts, photocatalytic efficiency is still low. Herein, a WO3/BiOBr S-scheme heterojunction was formed by combining WO3 with BiOBr, which facilitated the transfer and separation of photoinduced electrons and holes and enhanced the photocatalytic CO2 reaction. The optimized WO3/BiOBr heterostructures exhibited best activity for photocatalytic CO2 reduction without any sacrificial reagents, and the CO yield reached 17.14 µmol g-1 after reaction for 4 h, which was 1.56 times greater than that of BiOBr. The photocatalytic stability of WO3/BiOBr was also improved.

Preparation of porous superabsorbent particles based on starch by supercritical CO2 drying and its water absorption mechanism.

The slow water-absorption speed of starch-based superabsorbent resin (St-SAP) limits its application. In this study, porous St-SAP (P-St-SAP) was prepared by inverse suspension polymerization and supercritical CO2 drying, the aim is to provide a preparation method of fast absorbent resin. The P-St-SAP at 33 % starch content had an interpenetrating porous structure with macropores, mesopores and micropores, and the surface area, pore volume and average pore diameter were 32.06 m2·g-1, 0.116 cm3·g-1 and 21.6 nm, respectively. The water-absorption process included rapid-section, medium-section and slow-section, according with internal diffusion, double-constant and quasi second-order kinetic models, respectively. In the initial 30 s, a water-absorption speed of 262.6 g·g-1·min-1 in distilled water was much higher than some previous research results, and the equilibrium absorption value of 517.9 g·g-1 in distilled water and 72.9 g·g-1 in 0.9 % saline was better than that of non-porous St-SAP at similar starch content. Moreover, at the same stage the percentage of saline absorption ratio to equilibrium absorption value was 1.0- 2.0 times higher than that of distilled water. These research results indicate that the P-St-SAP has fast water-absorption speed and good salt resistance, which will have greater application prospects in sanitary materials, building concrete pouring, and flood control blocking piping.

Temperature-Sensitive Aerogel Using Bagasse Carboxylated Cellulose Nanocrystals/N-Isopropyl Acrylamide for Controlled Release of Pesticides.

Temperature-sensitive carboxylated cellulose nanocrystals/N-isopropyl acrylamide aerogels (CCNC-NIPAMs) were developed as novel pesticide-controlled release formulas. Ammonium persulfate (APS) one-step oxidation was used to prepare bagasse-based CCNCs, and then the monomer N-isopropyl acrylamide (NIPAM) was successfully introduced and constructed into the temperature-sensitive CCNC-NIPAMs through polymerization. The results of the zeta potential measurement and Fourier infrared transform spectrum (FTIR) show that the average particle size of the CCNCs was 120.9 nm, the average surface potential of the CCNCs was -34.8 mV, and the crystallinity was 62.8%. The primary hydroxyl group on the surface of the CCNCs was replaced by the carboxyl group during oxidation. The morphology and structure of CCNC-NIPAMs were characterized via electron microscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), compression performance, porosity analysis, and thermogravimetric (TG) analysis. The results demonstrate that CCNC-NIPAM has a high porosity and low density, as well as good thermal stability, which is conducive to loading and releasing pesticides. In the swelling, drug loading, and controlled release process, the CCNC-NIPAM exhibited significant temperature sensitivity. Under the same NIPAM reaction amount, the equilibrium swelling rate of the CCNC-NIPAM first increased and then decreased with increasing temperature, and the cumulative drug release ratio of the CCNC-NIPAM at 39 °C was significantly higher than that at 25 °C. The loading efficiency of the CCNC-NIPAM on the model drug thiamethoxam (TXM) was up to 23 wt%, and the first-order model and Korsmyer-Peppas model could be well-fitted in the drug release curves. The study provides a new method for the effective utilization of biomass and pesticides.

Phosphorus-Doped Hollow Tubular g-C3N4 for Enhanced Photocatalytic CO2 Reduction.

Photocatalytic CO2 reduction is a tactic for solving the environmental pollution caused by greenhouse gases. Herein, NH4H2PO4 was added as a phosphorus source in the process of the hydrothermal treatment of melamine for the first time, and phosphorus-doped hollow tubular g-C3N4 (x-P-HCN) was fabricated and used for photocatalytic CO2 reduction. Here, 1.0-P-HCN exhibited the largest CO production rate of 9.00 µmol·g-1·h-1, which was 10.22 times higher than that of bulk g-C3N4. After doping with phosphorus, the light absorption range, the CO2 adsorption capacity, and the specific surface area of the 1.0-P-HCN sample were greatly improved. In addition, the separation of photogenerated electron-hole pairs was enhanced. Furthermore, the phosphorus-doped g-C3N4 effectively activated the CO2 adsorbed on the surface of phosphorus-doped g-C3N4 photocatalysts, which greatly enhanced the CO production rate of photocatalytic CO2 reduction over that of g-C3N4.

Enhanced Water Absorbency and Water Retention Rate for Superabsorbent Polymer via Porous Calcium Carbonate Crosslinking.

To improve the water absorbency and water-retention rate of superabsorbent materials, a porous calcium carbonate composite superabsorbent polymer (PCC/PAA) was prepared by copolymerization of acrylic acid and porous calcium carbonate prepared from ground calcium carbonate. The results showed that the binding energies of C-O and C=O in the O 1s profile of PCC/PAA had 0.2 eV and 0.1-0.7 eV redshifts, respectively, and the bonding of -COO- groups on the surface of the porous calcium carbonate led to an increase in the binding energy of O 1s. Furthermore, the porous calcium carbonate chelates with the -COO- group in acrylic acid through the surface Ca2+ site to form multidirectional crosslinking points, which would increase the flexibility of the crosslinking network and promote the formation of pores inside the PCC/PAA to improve the water storage space. The water absorbency of PCC/PAA with 2 wt% porous calcium carbonate in deionized water and 0.9 wt% NaCl water solution increased from 540 g/g and 60 g/g to 935 g/g and 80 g/g, respectively. In addition, since the chemical crosslinker N,N'-methylene bisacrylamide is used in the polymerization process of PCC/PAA, N,N'-methylene bisacrylamide and porous calcium carbonate enhance the stability of the PCC/PAA crosslinking network by double-crosslinking with a polyacrylic acid chain, resulting in the crosslinking network of PCC/PAA not being destroyed after water absorption saturation. Therefore, PCC/PAA with 2 wt% porous calcium carbonate improved the water-retention rate by 244% after 5 h at 60 °C, and the compressive strength was approximately five-times that of the superabsorbent without porous calcium carbonate.

Nanostructure Design of Catalysts: Latest Advances and Prospects.

The recent development of nanotechnology has laid the foundation for the design and preparation of various nanostructured materials [...].

Characterization of Modified Mechanically Activated Cassava Starch Magnetic Porous Microspheres and Its Adsorption for Cd(II) Ions.

The magnetic polymer microsphere is a promising adsorbent due to its high adsorption efficiency and good regeneration ability from wastewater. Cassava starch magnetic porous microspheres (AAM-MSMPMs) were synthesized by graft copolymerization in inverse emulsion. Mechanically activated cassava starch (MS) was used to graft skeletons, vinyl monomers [acrylic acid (AA) and acrylamide (AM)] as copolymerized unsaturated monomers, methyl methacrylate (MMA) as the dispersing agent, and polyethylene glycol/methanol (PEG2000/MeOH) as the porogen. It was found that the AAM-MSMPM adsorbent is superparamagnetic, the saturation magnetization is 14.9 emu·g-1, and it can be rapidly and directionally separated from Cd(II) ions in aqueous solution. The FTIR indicated that the carboxyl and hydroxyl groups were grafted into MS. The AAM-MSMPM had good speroidization and a uniform size. After the porogen was added, the particle size of the AAM-MSMPM decreased from 19.00 to 7.00 nm, and the specific surface area increased from 7.00 to 35.00 m2·g-1. The pore volume increased from 0.03 to 0.13 cm3·g-1. The AAM-MSMPM exhibited a large specific surface area and provided more adsorption active sites for Cd(II) ions. The maximum adsorption capacity of the AAM-MSMPM for Cd(II) ions was 210.68 mg·g-1, i.e., 81.02% higher than that without porogen. Additionally, the Cd(II) ion adsorption process on the AAM-MSMPM can be described by Langmuir isothermal and pseudo-second-order kinetic models. A chemical reaction dominated the Cd(II) ion adsorption process on the AAM-MSMPM, and chemisorption was the rate-controlling step during the Cd(II) ion adsorption process. The AAM-MSMPM still had excellent stability after five consecutive reuses.

Ni-Ti Intercalated and Supported Bentonite for Selective Hydrogenation of Cinnamaldehyde.

Ni-Ti intercalated bentonite catalysts (Ni-Ti-bentonite) and Ni-TiO2 supported bentonite catalysts (Ni-TiO2 /bentonite) were prepared, and the effects of Ni-Ti supported and intercalated bentonite on the selective hydrogenation of cinnamaldehyde were investigated. Ni-Ti intercalated bentonite enhanced the Brønsted acid sites strength, decreased the acid amount and Lewis's acid sites strength, which inhibited the activation of the C=O bond and contributed to selective hydrogenation of the C=C bond. When Ni-TiO2 was supported on bentonite, the acid amount and Lewis's acid strength of the catalyst increased, providing additional adsorption sites and increased the acetals byproducts. Due to the higher surface area, mesoporous volume, and suitable acidity, compared with Ni-TiO2 /bentonite in methanol solvent, 2 MPa, 120 °C for 1 h, Ni-Ti-bentonite exhibited a higher cinnamaldehyde (CAL) conversion of 98.8 %, as well as a higher hydrocinnamaldehyde (HCAL) selectivity of 95 %, and no acetals were found in the product.

Fe2O3 supported Pt single atom catalysts for the selective hydrogenation of cinnamaldehyde.

Atomically dispersed Pt species supported on Fe2O3 (Pt1/Fe2O3) are successfully constructed by a simple ball milling process. In the selective hydrogenation of cinnamaldehyde (CAL), Pt1/Fe2O3 achieves an excellent cinnamyl alcohol (COL) selectivity of 81.7% at a CAL conversion of 91.2% in pure water medium due to the superior dissociation ability of H2 and preferential adsorption of CAL via CO.

Structure identification and analysis of the suspected chemical precursor of 2-fluorodeschloroketamine and its decomposition products.

In this work, 1-[(2″-fluorophenyl)(methylimino)methyl]cyclopentan-1-ol (2-fluorodeschlorohydroxylimine) was identified as a suspected chemical precursor of 2-fluorodeschloroketamine (2-FDCK) using gas chromatography-mass spectrometry (GC-MS) and gas chromatography-quadrupole/time-of-flight mass spectrometry (GC-Q/TOF-MS) and comparing the data with those of ketamine and its chemical precursor, hydroxylimine. Furthermore, the entire fragmentation pathway of 2-fluorodeschlorohydroxylimine was theorized from the GC-MS spectrum recorded using an electron ionization (EI) source, and the mechanisms and decomposition pathways of 2-fluorodeschlorohydroxylimine were elucidated. In protic solvents, the nitrogen atom in the C═N group of 2-fluorodeschlorohydroxylimine underwent a protonation reaction. Thereafter, the traces of water present in protic solvents promoted the hydrolysis of the protonated imine, and a carbon cation was obtained following the loss of methylamine. The carbon cation could follow the classical decomposition mechanism of imines and yield an α-hydroxyl ketone, which was the major decomposition product, (2'-fluorophenyl)(1″-hydroxycyclopentyl)methanone. The cation could also undergo a loop expansion rearrangement and yield another α-hydroxyl ketone, 2-(2'-fluorophenyl)-2-hydroxycyclohexan-1-one. The structures of the two aforementioned decomposition products were elucidated using several techniques including theoretical calculation, GC-MS, nuclear magnetic resonance (NMR), the prediction and assistance elucidation functions of ACDLabs-Structure Elucidator Suite, and the virtual separation technology of diffusion-ordered spectroscopy. The aforementioned study revealed important information about the chemical precursor of 2-FDCK and its decomposition. Furthermore, a set of methods for the qualitative analysis of 2-fluorodeschlorohydroxylimine were established, which facilitated accurate analysis of 2-fluorodeschlorohydroxylimine samples following decomposition or destruction.

Sulfur Vacancy and Ti3 C2 Tx Cocatalyst Synergistically Boosting Interfacial Charge Transfer in 2D/2D Ti3 C2 Tx /ZnIn2 S4 Heterostructure for Enhanced Photocatalytic Hydrogen Evolution.

Constructing an efficient photoelectron transfer channel to promote the charge carrier separation is a great challenge for enhancing photocatalytic hydrogen evolution from water. In this work, an ultrathin 2D/2D Ti3 C2 Tx /ZnIn2 S4 heterostructure is rationally designed by coupling the ultrathin ZnIn2 S4 with few-layered Ti3 C2 Tx via the electrostatic self-assembly strategy. The 2D/2D Ti3 C2 Tx /ZnIn2 S4 heterostructure possesses larger contact area and strong electronic interaction to promote the charge carrier transfer at the interface, and the sulfur vacancy on the ZnIn2 S4 acting as the electron trap further enhances the separation of the photoinduced electrons and holes. As a consequence, the optimal 2D/2D Ti3 C2 Tx /ZnIn2 S4 composite exhibits a high photocatalytic hydrogen evolution rate of 148.4 µmol h-1 , which is 3.6 times and 9.2 times higher than that of ZnIn2 S4 nanosheet and flower-like ZnIn2 S4 , respectively. Moreover, the stability of the ZnIn2 S4 is significantly improved after coupling with the few-layered Ti3 C2 Tx . The characterizations and density functional theory calculation demonstrate that the synergistic effect of the sulfur vacancy and Ti3 C2 Tx cocatalyst can greatly promote the electrons transfer from ZnIn2 S4 to Ti3 C2 Tx and the separation of photogenerated charge carriers, thus enhancing the photocatalytic hydrogen evolution from water.

Prepared self-growing supported nickel catalyst by recovering Ni (â ¡) from metal wastewater using geopolymer microspheres.

Here, new and effective microsphere adsorbents were synthesized by NaOH activating slag based geopolymer (Na-SGS). These microsphere adsorbents upset the adsorption equilibrium with the maximum Ni2+ adsorption capacity of 414.38 mg/g which is much larger than that of other geopolymer materials. After Ni2+ adsorption from simulated nickel electroplating wastewater, more active positions for the adsorption Ni2+ ions on Na-SGS were provided as shifts from the average pore diameter of 22.00-7.44 nm, the pore volume of 0.06 to 0.25 cm3/g, the Brunauer-Emmett-Teller (BET) surface area of 10.46-125.35 m2/g and the apparent change of new morphology. Moreover, the adsorbed Ni2+ species were distributed uniformly on Na-SGS. Thermodynamic performance reflected an exothermic, spontaneous and molecular disorder adsorption process, which can be easily controlled by the pH, dosage, initial concentration, contact time and temperature. Through the controllable adsorption, Na-SGS after Ni2+ adsorption (Na-SGS-Ni) was recycled and then reduced to be directly supported nickel catalysts (red-Na-SGS-Ni), which showed superior catalytic activity for CO2 methanation. Although the highest percent of CO2 conversation (XCO2 =99.54%) and methane selectivity (SCH4 =99.5%) are both at 300 °C, red-Na-SGS-Ni performed good XCO2 (99.48%) and SCH4 (98.2%) at low temperatures (100 °C).

An overview of photocatalysis facilitated by 2D heterojunctions.

Two-dimensional (2D) photocatalysts have attracted considerable research interest in the past decades due to their unique optical, physical and chemical properties. Constructing 2D/2D heterojunctions with large interface area has been considered as an effective approach to enhance the transfer rate and the separation efficiency of the charge carriers, leading to dramatic increase in the photocatalytic performance of the photocatalysts. Here, the state-of-the-art progress on heterojunctions based on 2D materials is reviewed, including the photocatalysis principles using 2D heterojunctions, the categories of 2D heterojunctions and their application in different photocatalytic reactions, and the theoretical studies of the 2D heterojunctions. Moreover, the advantages and disadvantages of the 2D heterojunctions are also discussed. Finally, the ongoing challenges and opportunities for the future development of 2D photocatalysts with built-in heterojunctions are proposed.

2D/2D heterojunction of Ti3C2/g-C3N4 nanosheets for enhanced photocatalytic hydrogen evolution.

Photocatalytic hydrogen evolution from water has received enormous attention due to its ability to address a number of global environmental and energy-related issues. Here, we synthesize 2D/2D Ti3C2/g-C3N4 composites by electrostatic self-assembly technique and demonstrate their use as photocatalysts for hydrogen evolution under visible light irradiation. The optimized Ti3C2/g-C3N4 composite exhibited a 10 times higher photocatalytic hydrogen evolution performance (72.3 µmol h-1 gcat-1) than that of pristine g-C3N4 (7.1 µmol h-1 gcat-1). Such enhanced photocatalytic performance was due to the formation of 2D/2D heterojunctions in the Ti3C2/g-C3N4 composites. The intimate contact between the monolayer Ti3C2 and g-C3N4 nanosheets promotes the separation of photogenerated charge carriers at the Ti3C2/g-C3N4 interface. Furthermore, the ultrahigh conductivity of Ti3C2 and the Schottky junction formed between g-C3N4/MXene interfaces facilitate the photoinduced electron transfer and suppress the recombination with photogenerated holes. This work demonstrates that the 2D/2D Ti3C2/g-C3N4 composites are promising photocatalysts thanks to the ultrathin MXenes as efficient co-catalysts for photocatalytic hydrogen production.

One-Step Synthesis of Nb2 O5 /C/Nb2 C (MXene) Composites and Their Use as Photocatalysts for Hydrogen Evolution.

Hydrogen production through facile photocatalytic water splitting is regarded as a promising strategy to solve global energy problems. Transition-metal carbides (MXenes) have recently drawn attention as potential co-catalyst candidates for photocatalysts. Here, we report niobium pentoxide/carbon/niobium carbide (MXene) hybrid materials (Nb2 O5 /C/Nb2 C) as photocatalysts for hydrogen evolution from water splitting. The Nb2 O5 /C/Nb2 C composites were synthesized by one-step CO2 oxidation of Nb2 CTx . Nb2 O5 grew homogeneously on Nb2 C after mild oxidation, during which some amorphous carbon was also formed. With an optimized oxidation time of 1.0 h, Nb2 O5 /C/Nb2 C showed the highest hydrogen generation rate (7.81 µmol h-1 gcat-1 ), a value that was four times higher than that of pure Nb2 O5 . The enhanced performance of Nb2 O5 /C/Nb2 C was attributed to intimate contact between Nb2 O5 and conductive Nb2 C and the separation of photogenerated charge carriers at the Nb2 O5 /Nb2 C interface; the results presented herein show that transition-metal carbide are promising co-catalysts for photocatalytic hydrogen production.

Low temperature CO oxidation catalysed by flower-like Ni-Co-O: how physicochemical properties influence catalytic performance.

In this work, mesoporous Ni-Co composite oxides were synthesized by a facile liquid-precipitation method without the addition of surfactant, and their ability to catalyse a low temperature CO oxidation reaction was investigated. To explore the effect of the synergetic interaction between Ni and Co on the physicochemical properties and catalytic performance of these catalysts, the as-prepared samples were characterized using XRF, XRD, LRS, N2-physisorption (BET), SEM, TEM, XPS, H2-TPR, O2-TPD and in situ DRIFTS characterization techniques. The results are as follows: (1) the doping of cobalt can reduces the size of NiO, thus massive amorphous NiO have formed and highly dispersed on the catalyst surface, resulting in the formation of abundant surface Ni2+ ions; (2) Ni2+ ions partially substitute Co3+ ions to form a Ni-Co spinel solid solution, generating an abundance of surface oxygen vacancies, which are vital for CO oxidation; (3) the Ni0.8Co0.2 catalyst exhibits the highest catalytic activity and a satisfactory stability for CO oxidation, whereas a larger cobalt content results in a decrease in activity, suggesting that the amorphous NiO phase is the dominant active phase instead of Co3O4 for CO oxidation; (4) the introduction of Co can alter the morphology of catalyst from plate-like to flower-like and then to dense granules. This morphological variation is related to the textural properties and catalytic performance of the catalysts. Lastly, a possible mechanism for CO oxidation reaction is tentatively proposed.

Intrinsic Kinetics of Dimethyl Ether Synthesis from Plasma Activation of CO2 Hydrogenation over Cu-Fe-Ce/HZSM-5.

CO2 is activated in a plasma reactor followed by hydrogenation over a Cu-Fe-Ce/HZSM-5 catalyst, and the intrinsic kinetics of the plasma catalytic process are studied. Compared with CO2 hydrogenation using Cu-Fe-Ce/HZSM-5 alone, the CO2 conversion and the dimethyl ether selectivity for the plasma catalytic process are increased by 16.3 %, and 10.1 %, respectively, indicating that the CO2 was activated by the plasma to promote hydrogenation. A study of the intrinsic kinetics shows that the activation energies of methanol formation, the reverse water-gas shift reaction, and methanol dehydration to dimethyl ether are 149.34, 75.47, and 73.18 kJ mol-1 , respectively, which are lower than if Cu-Fe-Ce/HZSM-5 is used without plasma, indicating that the activation of CO2 in the plasma reduces the activation energy of the hydrogenation reaction and improves the yield of dimethyl ether.