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[Display omitted] The quest for efficient hydrogen production highlights the need for cost-effective and high-performance catalysts to enhance the electrochemical water-splitting process. A significant challenge in developing self-supporting catalysts lies in the high cost and complex modification of traditional substrates. In this study, we developed catalysts featuring superaerophobic microstructures engineered on microspherical nickel-coated Chinese rice paper (Ni-RP), chosen for its affordability and exceptional ductility. These catalysts, due to their microspherical morphology and textured surface, exhibited significant superaerophobic properties, substantially reducing bubble adhesion. The nickel oxy-hydroxide (NiO x H y) and phosphorus-doped nickel (PNi) catalysts on Ni-RP demonstrated effective roles in oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), achieving overpotentials of 250 mV at 20 mA cm−2 and 87 mV at −10 mA cm−2 in 1 M KOH, respectively. Moreover, a custom water-splitting cell using PNi/Ni-RP and NiO x H y /Ni-RP electrodes reached an impressive average voltage of 1.55 V at 10 mA cm−2, with stable performance over 100 h in 1 M KOH. Our findings present a cost-effective, sustainable, and easily modifiable substrate that utilizes superaerophobic structures to create efficient and durable catalysts for water splitting. This work serves as a compelling example of designing high-performance self-supporting catalysts for electrocatalytic applications. [ABSTRACT FROM AUTHOR]

The electrochemical carbon dioxide reduction reaction (CO2RR) holds substantial promise for producing high‐value chemicals and fuels, drawing significant attention from both academia and industry. This work proposes an in‐situ electrodeposition method to prepare indium‐doped copper (Cu)‐based catalysts on carbon paper (Cu100Inx−CP, x=3.9, 4.5, 4.8, 5.1, and 7.6, denoting the molar ratio of In to Cu in the catalyst.). The catalysts Cu100Inx−CP were used for CO2RR to produce multi‐carbon (C2+) products. Characterization results showed that In was highly dispersed in the Cu particles at x<5.1. The Cu100In5.1−CP (containing 0.95 wt % In based on Cu) was very efficient for electrocatalytic CO2RR. The in‐situ Raman spectroscopy showed that Cu100In5.1−CP enhanced *CO intermediate adsorption and promoted the production of C2+ products due to the synergistic effect between In and Cu. In doping could suppress HER, enhanced *CO intermediate adsorption, and C−C coupling for the production of C2+ products in CO2RR. [ABSTRACT FROM AUTHOR]

Micro Fuel cells or microfluidic fuel cells (μMFCs) are one of the most promising power supplies for portable electronics. However, the necessary electrode spacing is required to prevent fuel-crossover and maintain the stable operation, introducing the unavoidable ohmic resistance and retarding the miniaturization. Herein, we propose a novel μMFC device combining the cellulose paper as separator, with selective catalysts at the cathode side to eliminate the unwanted side reactions and increase the system compactness. One single reactant solution containing fuel and electrolyte is applied to keep the device stable operation. The power-generation properties are evaluated in typical alkaline conditions. A great construction simplification makes the device a substantial high-power density of 2.14 W cm−3 and maximum current density of 15.82 A cm−3. The μMFC stacks are arranged in series and parallel manners, which delivers a maximum power output of 23.6 mW and current of 194.6 mA. It is expected that innovative and customizable performance from commercial paper and low-cost carbonaceous catalysts can provide a forum for future advancement in chip-based electrochemical energy generation and storage devices. • Filter paper served as a membrane for μMFC is proposed. • The electrode-pair distance is greatly minimized (∼140 μm). • The optimized μMFC delivers an ultrahigh power density of 2.14 W cm−3. • The μMFC stacks power output of 23.6 mW and current output of 194.6 mA are achievable. [ABSTRACT FROM AUTHOR]

Conventional Al‐air batteries are not suitable as portable power devices due to their complicated water management and bulky system. To resolve this issue, the fiber paper‐ and cotton cloth‐based Al‐air batteries were proposed, which exploited the capillary force from the paper (FP) and cotton cloth (CC) to deliver the solutions and eliminated the external pump. The physical features of the FP and CC were gained including the surface morphologies, surface elementary analysis, liquid absorption and flow rates. CC owned larger liquid absorption and faster flow rate due to its hierarchically woven‐spun fiber structure, compared to the randomly oriented fibers of the FP, although the surface of the CC demonstrated lower O/C ratio than that of the FP. So, the performance of the CC‐based Al‐air battery was largely higher than that of the FP‐based battery. The performance of the CC‐based Al‐air battery was optimal at 1.0 M NaOH electrolyte and the anode‐to‐cathode surface area ratio of 1 : 4, with the peak power density of 14.95±0.28 mW cm−2, and the maximum current density of 36.61±0.54 mA cm−2. To apply the CC‐based Al‐air battery, the two‐battery pack connected in series was assembled to drive a timer and light 9 LEDs. [ABSTRACT FROM AUTHOR]

Fibers represent a type of structure of great interest in catalysis since they combine high area to volume ratio and can be fabricated from many types of materials, such as ceramic oxides, polymers, and alloys. They can be used in isolated form or structured, as in the case of the ceramic papers synthesized in this work, following a modified papermaking technique. The addition of cationic and anionic polyelectrolytes improved the retention of ceramic fibers during the ceramic paper formation stage by adsorption processes, through the formation of floccules. In the complex aqueous system containing charged macromolecules, the amounts of polyelectrolytes to be added were determined by titrations. To enhance mechanical properties of ceramic papers, different classes of nanoparticle suspensions can be used as binders. As a novel alternative, we have used different borate-type compounds. Among them, we selected natural ulexite, which was purified and used as a binder of ceramic fibers. In order to improve mechanical resistance and flexibility, measured from tensile indexes and elastic module, the amounts of NaCaB5O6(OH)6.5H2O and the calcination temperature were varied. In this contribution, to take advantage of the unique characteristics of the ulexite-containing ceramic papers, they were impregnated with Co,Ce and Co,Ba,K and tested for diesel soot combustion. [ABSTRACT FROM AUTHOR]

The present study reports the catalytic activity and stability of Mn–Ce catalyst with low Mn content in the soot combustion reaction. Through X-ray diffraction analysis (XRD), Laser Raman Spectroscopy (LRS), and Temperature-Programmed Reduction studies (CO-TPR), it is inferred that the Mn/(Mn + Ce) ratio = 0.1 allows the formation of a solid solution between Mn and Ce oxides with high catalytic performance. This formulation was structured over ceramic papers to conform catalytic ceramic papers. These structured fibrous catalysts presented high catalytic stability after several cycles of the soot combustion reaction and they prove to be highly active in the reaction of interest. Their catalytic performance under different oxidation conditions was also evaluated by varying the NO and O2 proportion in the gas feed. The NO content in the gas feed considerably influenced the catalytic performance and the reaction order with respect to this oxidant was ca. 0.3. The activation energy was found to be 14 kcal/mol. [ABSTRACT FROM AUTHOR]

• The hygroscopic property of paper fiber is used to prepare a bifunctional catalyst. • The impregnation time for preparing the hollow microtubular Ni-MgO-CaO is 1 min. • 94.1 % of hydrogen is stably produced on 5Ni-10MgO-CaO from biogas for 50 cycles. • Only 37.1 % loss of the sorption-enhanced effect is shown during the entire cycle. Sorption-enhanced steam reforming (SESR) process is a promising technology aiming at the production of high purity hydrogen with CO 2 capture. The key to the success of this process is the availability of high-performance bifunctional catalysts. Herein, we develop a hollow microtubular Ni-MgO-CaO bifunctional catalyst with paper fiber as template. Due to the strong hygroscopic properties of paper fibers, it provides a method for the rapid synthesis of catalysts with design components by adsorbing solution. The characterizations indicate that the impregnation time (1 min vs 24 h) has no effect on the structural properties of Ni-MgO-CaO bifunctional catalysts. MgO as an inert spacer can weaken the sintering of CaO to ensure a stable CO 2 uptake. Moreover, the agglomeration of Ni particles is inhibited by the MgO coating on their surface. 5Ni-10MgO-CaO as the best performing catalyst displays high stability for the SESR of biogas (SESRB) reaction, during which 94.1 % purity of hydrogen with a 95.2 % conversion of CH 4 is stably produced and only 37.1 % decrease of sorption-enhanced effect is observed in 50 SESRB-calcination cycles. [ABSTRACT FROM AUTHOR]

The metal-organic frameworks (MOFs) nanozyme-mediated paper-based analytical devices (PADs) have shown great potential in portable visual determination of phenolic compounds in the environment. However, most MOF nanozymes suffer from poor dispersibility and block-like structure, which often prompts deposition and results in diminished enzymatic activity, severely hindering their environmental applications. Here, we proposed colorimetric PADs for the visual detection of dichlorophen (Dcp) based on its significant inhibitory effect on the two-dimensional (2D) MOF nanozyme activity. Specifically, we synthesized a 2D Cu TCPP (Fe) (defined as 2D-CTF) MOF nanozyme exhibiting excellent dispersibility and remarkable peroxidase-like (POD-like) activity, which could catalyze the oxidation and subsequent color change of 3,3′,5,5′-tetramethylbenzidine even under neutral conditions. Notably, the POD-like activity of 2D-CTF demonstrated a unique response to Dcp because of the occupation of Fe–N 4 active sites on the 2D-CTF. This property enables the use of 2D-CTF as a highly efficient catalyst to develop colorimetric PADs for naked-eye and portable detection of Dcp. We believe that the proposed colorimetric PADs offer an efficient method for Dcp assay and open fresh avenues for the advancement of colorimetric sensors for analyzing of phenolic toxic substances in real samples. [ABSTRACT FROM AUTHOR]

Sluggish CO2 reduction reaction (CO2RR) and evolution reaction (CO2ER) kinetics at cathodes seriously hamper the applications of Li-CO2 batteries, which have attracted vast attention as one kind of promising carbon-neutral technology. Two-dimensional transition metal dichalcogenides (TMDs) have shown great potential as the bidirectional catalysts for CO2 redox, but how to achieve a high exposure of dual active sites of TMDs with CO2RR/CO2ER activities remains a challenge. Herein, a bidirectional catalyst that vertically growing MoS2 on Co9S8 supported by carbon paper (V-MoS2/Co9S8@CP) has been designed with abundant edge as active sites for both CO2RR and CO2ER, improves the interfacial conductivity, and modulates the electron transportation pathway along the basal planes. As evidenced by the outstanding energy efficiency of 81.2% and ultra-small voltage gap of 0.68 V at 20 µA cm-2, Li-CO2 batteries with V-MoS2/Co9S8@CP show superior performance compared with horizontally growing MoS2 on Co9S8 (H-MoS2/Co9S8@CP), MoS2@CP, and Co9S8@CP. Density functional theory calculations help reveal the relationship between performance and structure and demonstrate the synergistic effect between MoS2 edge sites and Co9S8. This work provides an avenue to understand and realize rationally designed electronic contact of TMDs with specified crystal facets, but more importantly, provides a feasible guide for the design of high-performance cathodic catalyst materials in Li-CO2 batteries. [ABSTRACT FROM AUTHOR]

A series of thin Pt-Co films with different metal ratios were deposited by using the sequential cosputtering directly on a commercial hydrophobic carbon paper substrate at room temperature and in ultra-high vacuum (UHV) conditions. Their electrocatalytic properties toward the oxygen reduction reaction were investigated in 0.5 M H2SO4 solution by means of cyclic voltammetry (CV) and linear sweep voltammetry (LSV) on rotating disc electrode (RDE). The results showed that Pt particles, deposited by dc-magnetron gun, surround the large Co-clusters deposited by rf-magnetron gun. In addition, the increase of Co content led to an increase in the electrochemical active surface area (EASA) from 23.75 m2/gPt to 47.54 m2/gPt for pure Pt and Pt:Co (1:3), respectively, which corresponded the improvement of the utilization of Pt by a factor of 1.91. This improvement indicated that the sequential magnetron cosputtering was one of the essential technique to deposit homogeneous metal clusters with desirable size on the gas diffusion layer by adjustment plasma parameters. [ABSTRACT FROM AUTHOR]

Hallmark of a successful catalyst is its high efficiency, economic aspects, operational simplicity, extensive reusability, higher environment friendliness, and potential use in multiple industrial applications. Herein, a facile protocol involving a catalyst with Pd nanoparticles supported on cellulose paper (also known as a "dip‐catalyst") for the hydrogenation of a series of quinolines, nitroarene, and C−C bond formation reactions in most benign solvents such as water is described. The mere insertion/removal of the "dip‐catalyst" strip enables instantaneous start/stop of the reaction, which enhances its reusability and ease of separation of products. Cellulose paper (CP) strips decorated with Pd nanoparticles (Pd/CP) are prepared by the reduction of K2PdCl4 soaked strips using formic acid as reductant. The resulting spherical shaped Pd particles, confirmed by scanning electron microscopy, form stable catalysis centers on the support. XRD signature confirms the crystallinity of the Pd nanoparticles and the TEM images display 15–20 nm size particles uniformly decorating CP. X‐ray photoelectron spectroscopy indicates the formation of metallic Pd. The catalyst is tested for the C−C bond formation reactions. Pd/CP catalyzed Suzuki‐Miyaura coupling reaction demonstrate >99% conversion with optimum selectivity. On the other hand, Mizoroki‐Heck reaction produced 87% conversion with the reaction of 4‐methoxycarbonyl phenylboronic acid and iodobenzene in ethanol:water (1 : 1 v/v) using KOH as base. The developed Pd/CP construct produces >99% of the pyridine‐ring hydrogenated product on quinoline hydrogenation using tetrahydroxydiboron (THDB) as the hydrogen source. Diverse and highly reducible functional groups were also evaluated for transfer hydrogenation, which demonstrates a high efficiency in terms of both reactivity and selectivity. The used catalysts are recyclable for the multiple cycles. [ABSTRACT FROM AUTHOR]

This study reports the synthesis of bacterial cellulose (BC) hydrogel sheets and their utilization as a support for silver‑nickel oxide nanocomposites (Ag/NiO). A two-step facile hydrothermal method was employed for the preparation of Ag/NiO, followed by impregnation into BC hydrogel sheets. A 20% Ag/NiO composition was revealed by dry weight analysis. The stability of nanocomposites-Hydrogel was confirmed by Ag+ and Ni2+ ion release study. The catalytic activity of the BC-Ag/NiO was evaluated against chemical reduction of congo red, methyl orange and methylene blue. The reduction reaction followed pseudo first order kinetics and k app values of 0.1147 min−1, 0.1323 min−1 and 0.12989 min−1 were obtained for CR, MO, and MB dyes, respectively. The BC-Ag/NiO catalyst could be easily recovered and re-used in another reaction without centrifugation. The synthesized nanocomposites hydrogel was also tested for its antibacterial activity against Gram-negative bacteria, Escherichia coli (E.coli) and Gram-positive bacteria, Staphylococcus aureus (S.aureus). [ABSTRACT FROM AUTHOR]

A combination of multiple methods can greatly intensify the removal efficiency of hazardous substances. Herein, the synergistic utilization of adsorption and catalysis achieved for the highly efficient removal of hexavalent chromium (Cr6+). A paper-based palladium nanoparticles/UiO-66-NH 2 (PdNPs/UiO-66-NH 2 /LP) composite catalyst was prepared using lignocellulose paper-based material (LP) for the loading of UiO-66-NH 2 MOFs materials, with the lignin in LP as the reducer for the in-situ synthesis of PdNPs (12.3 nm) on UiO-66-NH 2 MOF materials. Lignocellulose paper-based materials with high strength (82 N·m/g) realized low-cost and environmentally friendly preparation and guaranteed the practicability of PdNPs/UiO-66-NH 2 /LP composite catalyst. The prepared PdNPs/UiO-66-NH 2 /LP achieved high-efficiency catalytic activity for hazardous Cr6+ removal through a constructed adsorption-catalytic synergistic system, in which the removal efficiency of Cr6+ in 10 min was increased by 2 times compared with a composite catalyst without MOFs loading. Finally, the PdNPs/UiO-66-NH 2 /LP composite catalyst demonstrated the great efficiency and practicality of water pollution treatment through synergistic adsorption enrichment and catalytic reduction. [Display omitted] [ABSTRACT FROM AUTHOR]

A combination of multiple methods can greatly intensify the removal efficiency of hazardous substances. Herein, the synergistic utilization of adsorption and catalysis achieved for the highly efficient removal of hexavalent chromium (Cr6+). A paper-based palladium nanoparticles/UiO-66-NH 2 (PdNPs/UiO-66-NH 2 /LP) composite catalyst was prepared using lignocellulose paper-based material (LP) for the loading of UiO-66-NH 2 MOFs materials, with the lignin in LP as the reducer for the in-situ synthesis of PdNPs (12.3 nm) on UiO-66-NH 2 MOF materials. Lignocellulose paper-based materials with high strength (82 N·m/g) realized low-cost and environmentally friendly preparation and guaranteed the practicability of PdNPs/UiO-66-NH 2 /LP composite catalyst. The prepared PdNPs/UiO-66-NH 2 /LP achieved high-efficiency catalytic activity for hazardous Cr6+ removal through a constructed adsorption-catalytic synergistic system, in which the removal efficiency of Cr6+ in 10 min was increased by 2 times compared with a composite catalyst without MOFs loading. Finally, the PdNPs/UiO-66-NH 2 /LP composite catalyst demonstrated the great efficiency and practicality of water pollution treatment through synergistic adsorption enrichment and catalytic reduction. [Display omitted] [ABSTRACT FROM AUTHOR]

The electrochemical activity of catalysts strongly depends on the uniform distribution of monodisperse Pt nanoparticles without aggregates. Here, we propose a new hydrolysis-assisted smearing method for Pt loading on a free-standing paper-type electrode. Polyacrylonitrile (PAN)-based nanofiber paper was used as the electrode, and it acted as a Pt support. Hydrolysis of the electrode tripled the number of active nucleation sites for Pt adsorption on the PAN nanofibers, thereby significantly enhancing the wettability of the nanofibers. This facilitated the uniform distribution of Pt nanoparticles without aggregate formation up to 40 wt% (about 0.8 mg/cm2) with a particle size of about 3 nm. The catalytic current of the hydrolyzed Pt electrode in CH3OH/H2SO4 solution exceeded 213 mA/cm2 Pt mg, which was considerably greater than the current was 148 mA/cm2 Pt mg for an unhydrolyzed electrode. [ABSTRACT FROM AUTHOR]

A rapid in situ analytical method was developed for the detection of generated carcinogenic aromatic amines from banned azo dyes utilizing a photocatalytic reduction-based liquid microjunction surface sampling (LMJSS)–mass spectrometry (MS) system. We utilized photocatalytic reduction under UV irradiation with TiO2 as catalyst to have rapid and mild reduction of azo dyes. The reaction conditions were optimized to have complete photocatalytic reduction within 2–5 min in pure methanol at room temperature. TiO2 was immobilized in the inner wall of the capillaries in the LMJSS system to achieve in situ sampling–online rapid reduction–MS detection for aromatic amines originating from azo dyes in packaging surface. The yields of in-tube photocatalytic reduction were near 100% by delivering the azo dye extracts through the capillary at 1 μL/min under UV irradiation. With this design, in situ analysis was completed within 2 min via direct MS detection and 7 min via liquid chromatography (LC)–MS detection. The detection limits for five aromatic amines originating from four different azo dyes were in the range of 1–17 mg/kg with relative standard deviations (RSDs) < 8.5%. In the application of the new method, four carcinogenic aromatic amines were detected and identified in three commercial packaging materials, and the quantitation results were comparable with those obtained by the conventional chemical reduction–LC–MS method (relative recovery, 81–121%). Moreover, due to the spatial resolution of the present method with a flow probe, MS imaging was achieved demonstrating clear azo dye patterns of a lab-made sample. [ABSTRACT FROM AUTHOR]

Achieving an efficient catalyst in the ATRP system with a simple design, preparation from available materials, and high recyclability is a significant challenging issue. To attain the goal, herein, we used chitosan (CS)-modified cellulose filter paper (FP) as a green support for the synthesis of dip catalyst. The preparation of this catalyst involved surface treatment of the FP strips by CS coating through a dipping method, which increased the affinity of the substrate for adsorbing copper ions in the next step. The Cu@CS-FP catalyst was prepared without the requirement of any ligands. The synthesized dip-catalyst, in the form of the strips, was employed for the first time in the ATRP reaction of methyl methacrylate to assay catalytic activity. Catalytic insertion/ removal (ON/OFF) experiments were carried out during the polymerization. A reasonable control over the molecular weight with high conversion (68%) and polydispersity index of 1.32 under mild reaction conditions were obtained. Significantly, because of the facile separation of the catalyst, the amount of copper that remained in the polymer was very low (2.7 ppm). Also, the recyclability of the catalyst was investigated for five runs. The conversion in the final run was 64% without a loss of catalyst efficiency. [ABSTRACT FROM AUTHOR]

In this paper, ceria flowers containing nano-sized catalyst Ni particles were prepared on alumina-silica fiber network for production of hydrogen from biogas. The CeO 2 flowers were prepared using hydrothermal method and then NiO was loaded on the CeO 2 flowers by impregnation method. The Paper-structured catalysts (PSCs) were prepared from alumina-silica fibers and the CeO 2 –NiO flowers using conventional paper making method. The loaded NiO particles were uniformly dispersed on the CeO 2 flowers with the use of polyvinylpyrrolidone as a dispersion enhancer, which was observed by FE-SEM and EDX analysis. The NiO particles were then reduced into Ni by using H 2. The PSCs containing CeO 2 –Ni flowers with various Ni contents (2.1, 3.4, and 4.6%) were used for dry reforming of CH 4. It was found that 3.4% amount of Ni on the PSC was suitable for reforming reaction, and the higher amount of Ni (4.6%) did not increase the CH 4 conversion. The PSC with the CeO 2 flowers had porous structure and large surface area leading to the better dispersion of the Ni particles with smaller size. This helped increase in catalytic performance, prevention of agglomerated particle catalysts at high temperature and coke forming after a long time operation. The CH 4 conversion of the PSCs containing CeO 2 –NiO flowers in the dry reforming of CH 4 was much higher (nearly 90%) with a smaller Ni content in comparison with the PSC without the CeO 2 flowers (with higher Ni content of 8.6%). Moreover, the PSCs with the flowers exhibited an excellent catalytic stability with the degradation of CH 4 conversion of only 3.1% after 50 h of reforming. In addition, the high oxygen storage capacity and oxygen mobility of CeO 2 resulted in a partial removal of coke forming on the catalyst particles during reforming. This indicated that the catalytic activity of the Ni particles dispersed on the CeO 2 flowers for dry reforming of CH 4 was superior to that of various Ni-based catalyst systems which had much higher Ni contents. Therefore, it is possible to use the PSCs containing CeO 2 –Ni flowers to generate hydrogen for use as fuels from dry reforming of CH 4. Image 1 • 5 μm spherical CeO2 flowers had open porous structure and high surface area. • NiO particle catalysts were uniformly dispersed on the CeO2 flowers. • Paper-structured catalysts (PSC) with the dispersed flowers had a great porosity. • PSCs with small Ni content exhibited excellent catalytic activity in CH4 reforming. • PSCs exhibited degradation of CH4 conversion of only 3.1% after 50 h of reforming. [ABSTRACT FROM AUTHOR]

Three types of carbon nanotubes coated on paper-like sintered stainless steel fibers (PSSF) were synthesized and applied for continuous catalytic wet hydrogen peroxide oxidation (CWPO) of phenol. The novel metal-free nitrogen-doped carbon nanotube-coated PSSF catalyst (N-CNTs/PSSF) was designed by direct chemical vapor deposition using melamine as solid precursor for the first time, and CNTs/PSSF and Fe2O3-deposited CNTs/PSSF (Fe-CNTs/PSSF) catalysts were synthesized for comparison. Characterization results showed that all the catalysts exhibited three-dimensional networks structure, with nanotubes wrapping on the stainless steel fibers successfully, and the N-CNTs showed distinct irregular corrugated morphology with nitrogen-doping level about 5.18 at.%. CWPO of phenol revealed that the N-CNTs/PSSF catalyst achieved favorable catalytic activity and highest stability during 100-h reaction (phenol and TOC conversions reached about 90% and 50%, respectively), while phenol conversions of CNTs/PSSF and Fe-CNTs/PSSF catalysts decreased over time to 72% and 58%, respectively. The N-CNTs/PSSF catalyst also showed the lowest Fe weight loss ratio (about 2.44 wt%) among the three catalysts. The favorable catalytic results of N-CNTs/PSSF can be ascribed to the synergistic effects of the strong affinity toward polar molecules of N-CNTs, as well as the enhancement in contact efficiency associated with three-dimensional networks structure of the PSSF. [ABSTRACT FROM AUTHOR]

In this study, hydrogen harvesting from fermentation of sugarcane bagasse (SCB) was promoted by maintaining synergism between sulfonated graphene (SGR) catalyst and paper mill sludge (PMS). The sulfonic acid (–SO 3 H) groups in the catalyst played a major role in destructing the β-1,4 glycosidic bonds of sugarcane bagasse, releasing readily biodegradable sugars into the fermentation medium. The cellulose, hemicellulose, and lignin conversion efficiency were improved by 127.5%, 495.0%, and 109.2%, respectively with 20 mgSGR/gVS catalyst addition, compared with the control samples. These values were also higher than those obtained by non-sulfonated graphene catalyst. The hydrogenation of sugarcane bagasse was maximized at a sulfonated graphene catalyst dosage of 60 mgSGR/gVS, providing the highest hydrogen harvesting of 4104 ± 321 mL. This was associated with an increase of the Proteobacteria phyla up to 52.0%, Firmicutes phyla to 13.9%, and Acinetobacter sp. to 39.8% compared with only 37.0%, 11.3% and 11.1% in the control assay respectively. Moreover, sulfonated graphene catalyst supplementation promoted the acetate fermentation reaction pathway by increasing the acetate/butyrate ratio up to 4.1. Nevertheless, elevating the catalyst dosage up to 120 mgSGR/gVS reduced the hydrogen harvesting (1190 ± 92 mL) due to the release of furfural (1.76 ± 0.02 g/L) in the fermentation cultures, deteriorating the microbes' internal composition and metabolism bioactivities. Finally maximizing the hydrogen productivity from sugarcane bagasse is feasible by incorporation of paper mill sludge and sulfonated graphene catalyst at dosage not exceeding 60 mgSGR/gVS. However, investigating the recyclability and disposal of digestate containing sulfonated graphene catalyst and the associated economic feasibility needs more attention in the future. [Display omitted] • Sugarcane bagasse was fermented by paper mill sludge supported on sulfonated graphene. • Synergism between paper mill sludge/sulfonated graphene improved bio-H 2 by 4.8 times. • Sulfonated graphene promoted acetate fermentation (HAc/HBu of 4.1) and inhibited HPr. • Acinetobacter degrading phenol increased by 3.6 folds with sulfonated graphene catalyst. • MolDock visualized H-bonding in hydrogenase protein/sulfonated graphene interaction. [ABSTRACT FROM AUTHOR]

Molybdenum disulfide (MoS2) or tungsten disulfide (WS2), as a promising catalyst, is widely investigated for hydrogen evolution reaction (HER). In this work, a composite electrocatalysts MoxW1-xS2 is successfully decorated on carbon fiber paper (CFP) through a facile hydrothermal method. The three-dimensional porous CFP can enable the diffusion and penetration of electrolyte. Comparing with MoS2 and WS2 catalyst, the composite electrocatalyst MoxW1-xS2 nanosheets can expose the large number of electrochemically active sites. Hence, the as-prepared MoxW1-xS2/CFP (3:1) exhibit the outstanding HER catalytic activity with the small Tafel slope of 68 mV dec−1 and the low overpotential of − 178.4 ± 0.5 mV at a current density of 10 mA cm−2. Chronoamperometric current test for 18 h confirm the long-term stability of the composite electrocatalyst. [ABSTRACT FROM AUTHOR]

In this study, we report the findings that the C-N composites containing Ni and Co (Ni1Co1/C-N, Ni3Co1/C-N, Ni6Co1/C-N, Ni9Co1/C-N, NiCo0/C-N and Ni0Co/C-N) can be produced by direct pyrolysis of the NiCo-doped polyaniline (PANI) precursors in N2 atmosphere at 800C and show efficient electroactivity for oxygen reduction reaction (ORR) in alkaline media. Distribution and compositions of the catalysts were characterized by SEM, TEM, EDS and XRD techniques. The catalysts were loaded on carbon paper to prepare gas diffusion electrodes, in which electrocatalytic activity for ORR in alkaline media was investigated by voltammetric techniques. The ORR current density on these carbon paper-supported NiCo/C-N catalysts exhibits a linear increase with the negative shift of ORR potential. The ORR onset potential is around 0.2V (versus Ag/AgCl) in alkaline media. Among the prepared catalysts, the catalyst Ni6Co1/C-N presents the largest ORR current density, which is 68.5mAcm@0.8V (versus Ag/AgCl) in alkaline media. Moreover, Ni6Co1/C-N catalyst also presents good electrocatalytic activity stability for ORR. Ni/Co-doped C-N nanocomposite catalysts were prepared by direct pyrolysis of the mixture containing Ni/Co salts and polyaniline. The electrochemical test mold was used to study the ORR activity of the catalysts NiCo/C-N loaded on carbon paper. One side of the carbon paper modified with catalyst was in contact with the electrolyte while the other side was in contact with air. Among the prepared catalysts, the Ni6Co1/C-N catalyst shows the largest ORR current density of 68.5 mA cm-2@-0.8 V and high activity stability of ORR in alkaline media. [ABSTRACT FROM AUTHOR]

A flexible paper-structured catalyst (PSC) that can be applied to the anode of a solid oxide fuel cell (SOFC) was examined for its potential to enable direct internal reforming (DIR) operation. The catalytic activity of three types of Ni-loaded PSCs: (a) without the dispersion of support oxide particles in the fiber network (PSC-A), (b) with the dispersion of (Mg,Al)O derived from hydrotalcite (PSC B), and (c) with the dispersion of (Ce,Zr)O 2-δ (PSC C), for dry reforming of CH 4 was evaluated at operating temperatures of 650–800 °C. Among the PSCs, PSC-C exhibited the highest CH 4 conversion with the lowest degradation rate. The electrochemical performance of an electrolyte-supported cell (ESC) was evaluated under the flow of simulated biogas at 750 °C for cases without and with the PSCs on the anode. The application of the PSCs improved the cell performance. In particular, PSC-C had a remarkably positive effect on stabilizing DIRSOFC operation fueled by biogas. • Direct internal reforming (DIR) SOFC fueled by biogas has been investigated. • Paper-structured catalyst (PSC) was examined for the application to DIRSOFC. • Coking-tolerant PSC for dry reforming was developed by the dispersion of (Ce,Zr)O 2-δ. • On-paper synthesis of (Ce,Zr)O 2δ contributed to its higher dispersion. • Performance of DIRSOFC was stabilized by applying the developed PSC on anode. [ABSTRACT FROM AUTHOR]

Hydrogen fuel is a non-toxic and source-abundant energetic system, but for its applications in the industry, several issues related to its storage must be resolved. Compounds like NaBH 4 appear as promising hydrogen sources, while can release the latter rapidly under controllable conditions with the use of heterogeneous catalyst systems. In this work, we synthesized a Ni–CoP catalyst by electrodeposition in a three-step process on carbon paper as support. The materials were characterized via SEM-EDS, XRD, and XPS techniques, while the hydrogen evolution reaction (HER) from alkaline NaBH 4 solutions was tested as a batch experiment. Ni–CoP catalyst showed a high amount of H 2 generated in a short time (∼550 mL in 1 min) and remained at 78 and 54% of its initial performance after respectively 100 and 300 h of a continuous hydrolysis process. Our catalyst revealed exceptional performance and stability at higher temperatures and a long process time, which have been a rare subject of investigation in other reports for NaBH 4 hydrolysis in the past. This work paves a new perspective in studying catalysts for hydrogen generation from borohydrides. [Display omitted] • Ni–CoP catalyst was electrodeposited on a carbon support. • Material characterization proved the formation of desired active layers. • High efficiency and stability of the catalyst for a long-term NaBH 4 hydrolysis was revealed. [ABSTRACT FROM AUTHOR]

Transport planning as a formalised profession is relatively young and there is no doubt it has evolved over time. In Europe, Sustainable Urban Mobility Plans reflect a change in emphasis from keeping traffic moving to place-based, people-centric planning. Three new developments of significance present themselves to contemporary transport planning: the collision and merging of the digital age with the motor age; a widespread sense of deep (and possibly deepening) uncertainty about the future; and the imperative to address the climate emergency and decarbonise transport. Taken together, such developments are reflected in the recent notion of Triple Access Planning which sits within a so-called 'decide and provide' paradigm – contrasted with traditional transport planning within the 'predict and provide' paradigm. The world is changing significantly with a strong sense that transport planning needs to change accordingly. This paper draws upon the '7 Questions Interview' technique to explore with 23 practitioners in the UK their experience of transport planning practice over time, their hopes and fears for its future and what could be achieved, and their views on enablers of, and barriers to, positive change. The interviews reveal a strong sense that transport planning can face a Sisyphean (seemingly impossible) task of advocating measures that could push towards realisation of economic, social and environmental aspirations, only to find progress with measure approval and implementation thwarted by perennial challenges including lack of political will and public buy-in. While the three new developments mentioned represent potential catalysts for significant change, such change relies on multiple other factors. These include collaborative cross-sector working, a long-term perspective, appropriate funding and political agency, and enhanced communication skills to win hearts and minds. The paper concludes that Sisyphus may continue to struggle to push the transport planning boulder to the top of the hill; unless perhaps Hercules can lend a hand. • Transport planning is evolving in the face of changing circumstances in society. • There is a degree of consensus among transport practitioners on goals and obstacles. • The digital age, climate emergency and deep uncertainty may be catalysts for change. • Effectiveness of transport planning rests in the hands of the public and politicians. • The profession faces a sobering outlook that may be akin to the plight of Sisyphus. [ABSTRACT FROM AUTHOR]

Nowadays, hydrogen is gaining attention as one of the green energy alternatives within transition to a zero-emission economy. Increasing demand for hydrogen and its production has prompted the development of low-carbon strategies and technologies for hydrogen generation from hydrocarbons. This paper provides a thorough analysis of traditional and innovative methods for hydrogen production from fossil feedstock, reviewing the critical aspects and recent advancements in the field. The paper emphasizes the potential of in situ hydrogen generation as the most promising method, taking into account CO2 emission concerns. Additionally, this study explores the use of software packages for modeling hydrogen production, outlining their advantages and disadvantages and proposing the most favorable software for in situ hydrogen generation from hydrocarbons. Subsequent analysis sheds light on the effectiveness, economic viability, environmental impact, and future perspectives of various hydrogen production technologies. • Overview of hydrogen production technologies: conventional and innovative methods. • Key issues and best practices of the latest experimental and numerical studies. • Comparative analysis of various hydrogen production technologies and approaches. • Subsurface hydrogen generation has a great development potential. • There are methods for clean hydrogen production from hydrocarbon feedstock. [ABSTRACT FROM AUTHOR]

This paper assesses how strategic planning for nature can be improved for England's built and natural environment using mainstreaming and landscape-scale concepts. Whilst both concepts feature in academic literature, there has been limited attention on their role as catalytic agents for strategic planning. Addressing this gap, evidence is used from two stakeholder workshops involving 62 senior policy experts managing a range of operational and hypothetical strategic spatial planning challenges. The results reveal a significantly weakened strategic planning arena characterised by policy disintegration, short termism and uncertainty. Key findings highlight the fallacy of pursuing strategic planning for nature in isolation from wider policy integration fusing environmental, economic and social components from the outset. Current barriers to progress include institutional inertia, technocratic vocabularies and neoliberalist priorities exacerbated by a weak underlying theory. Conversely opportunities for mainstreaming processes may help knowledge generation and exchange within transdisciplinary partnerships, whilst landscape scale thinking can improve understanding of issues using natures inherent geometry transforming processes and outcomes. The paper recommends the adoption of strategic planning pathways using mainstreaming and landscape-scale approaches working in tandem. Whilst focused on the English context, our findings are transferable to other planning systems in the Global North, especially those championing neoliberal market led policies. [ABSTRACT FROM AUTHOR]

NaY zeolite-containing ceramic papers were prepared by a papermaking technique with a dual polyelectrolyte retention system that implied the use of cationic and anionic polymers. To improve their mechanical properties, we found that some borate compounds could be successfully used as ceramic binders. Three types of sodium and/or calcium borates were tested as binders: colemanite, nobleite, and anhydrous ulexite. The improvement in the mechanical properties depends both on the borate used and on the calcination temperature. By XRD it was determined that the faujasite structure collapsed after calcination at 700°C, which limited the final calcination temperature of zeolitic ceramic papers. Different amounts of NaY zeolite were added to ceramic papers and, as observed by SEM, faujasite particles were well distributed throughout the ceramic paper structure. Ceramic papers containing 1.2 wt.% zeolite after calcination at 650°C resulted in structured catalysts that were easy-to- handle, and which can be adapted to different conformations. [ABSTRACT FROM AUTHOR]

A novel MnOx-deposited paper-like stainless steel fibers entrapped activated carbon catalyst (Mn-GAC/PSSF) was synthesized by papermaking technology and incipient wetness impregnation (IM) method for methyl ethyl ketone (MEK) combustion, and Mn-deposited granular activated carbon catalyst (Mn-GAC) was prepared simultaneously as a contrast. Characterization of all the samples were carried out by using X-ray diffraction patterns (XRD), N 2 adsorption-desorption, scanning electron microscopy (SEM), H 2 -Temperature programmed reduction (TPR) and X-ray photoelectron spectra (XPS). SEM showed that the Mn oxides on the carbons were relatively well distributed as that on the stainless steel fibers. XPS indicated that the Mn coexisted as Mn3+ and Mn4+. The catalytic activity test for MEK combustion was carried out at atmospheric pressure in a continuous fixed bed stainless steel tube reactor, the results revealed that the Mn-GAC/PSSF catalysts were much more active than Mn-GAC catalyst due to the properties of excellent mass transfer and contacting efficiency offered by PSSF structure, and exhibited high selectivity for complete oxidation of intermediates. Catalyst with higher Mn loading presented higher catalyst activity, the conversion of MEK reached to 90% at 521 K over the 30%-Mn-GAC/PSSF catalysts, while it was 566 K and 530 K over the 10%-Mn-GAC/PSSF catalyst and 20%-Mn-GAC catalyst, respectively. • Microfibrous entrapped activated carbon catalyst (Mn-GAC/PSSF) were prepared. • The Mn-GAC/PSSF catalyst presents efficient activity for MEK oxidation. • Catalytic efficiency of Mn-GAC/PSSF is superior to granular Mn-GAC. [ABSTRACT FROM AUTHOR]

A paper-structured catalyst (PSC) for biogas reforming was prepared with the aim of improving coking tolerance. During the paper-making process using inorganic fibers, Ni-loaded (Ce,Zr)O 2–δ particles were synthesized via co-precipitation and subsequent chemical reduction (on-paper synthesis). The effects of the CeO 2 /ZrO 2 weight ratio during preparation and the Ni loading amount on the catalytic activity for dry reforming of CH 4 were investigated at 750 °C. A Ni loading of 6 wt% with CeO 2 /ZrO 2 ≥ 1 led to stable CH 4 conversion of 85% without coking under a gas hourly space velocity of 3800 h −1 . The oxygen storage capacity of the (Ce,Zr)O 2–δ particles dispersed in the inorganic fiber network may contribute to the oxidation of carbonaceous species deposited on the catalyst surface. [ABSTRACT FROM AUTHOR]

Abstract: Co-liquefaction of secondary pulp/paper-mill sludge (solids concentration: 1.6 wt%) and waste newspaper with a total solids concentration of 11.3 wt% was investigated with and without the addition of catalysts in a 75 ml Parr High-Pressure reactor at temperatures of 250–380 °C for 20 min. The yield of heavy oil (HO) without catalyst was between 16.7 and 28.0 wt% within this temperature range, and peaked at 350 °C. The addition of HCO2H, FeS, or KOH at 5 wt% of the total solids (on a dry basis) was found to enhance the HO yield at 300 °C, particularly HCO2H, which increased the yield of HO from 24.9 to 34.4 wt%. More interestingly, synergistic effects between secondary pulp/paper-mill sludge and waste newspaper were observed in the co-liquefaction operations. For example, the HO yield attained was 26.9 wt% at 300 °C in the co-liquefaction of the mixture of 33 wt% sludge and 67 wt% waste newspaper, and was noted to be 9 wt% and 6 wt% higher than the yields obtained from liquefaction of sludge and waste newspaper alone, respectively. The HOs from liquefaction or co-liquefaction at 300 °C for 20 min exhibited significantly higher energy contents (HHV ≥ 30 MJ/kg), almost doubled those (˜16 MJ/kg) of the original feedstocks. [Copyright &y& Elsevier]

In this study, a piece of filter paper with good flexibility and hygroscopicity was used to support catalysts after a pencil drawing process. A layer of thin Ni film was deposited on the surface of the conductive graphite layer using an electrochemical method at a negative potential. Pd nanoparticles with high electrocatalytic activity for NaBH4 oxidation were introduced by immersing the Ni film-graphite-filter paper (NGF) in PdCl2 solution to obtain a Pd-NGF (PNGF) electrode. The morphology and phase structure of PNGF were characterized using scanning electron microscopy (SEM) equipped with an energy dispersive X-ray spectrometer (EDS), transmission electron microscopy (TEM) and an X-ray diffractometer (XRD). The PNGF electrode was used as the anode in direct borohydride fuel cells (DBFCs), and the electrochemical properties for NaBH4 oxidation were determined by cyclic voltammetry (CV), chronoamperometry (CA) and electrochemical impedance spectroscopy (EIS). The oxidation current density reaches 550 mA cm−2 at −0.4 V when the electrolyte contains 2 mol dm−3 NaOH and 0.10 mol dm−3 NaBH4. [ABSTRACT FROM AUTHOR]

Paper has become the basic elixir in everyone's activities and usage of paper has increased day by day, the waste generated by paper is also enormous. The primary source of paper is wood (tree) yet, waste paper is environmentally good and biodegradable; however, it is the primary source of deforestation. Current research aims to find an alternate way to recycle paper in the biological approach. Hence in our work, twelve cellulose-producing bacteria were isolated, out of which one bacterial strain proved to be the best. Cellulase enzyme was extracted and purified, and used for enzymatic de-inking of photocopy papers. The optimal conditions for cellulase synthesis were at 60 °C, glucose as the only carbon source, and potassium nitrate as the nitrogen source. The enzyme demonstrated excellent de-inking at a lower pulp consistency of 3% with a 20% enzyme dose. The cellulose and hemicellulose levels decreased, which can be attributed to fiber breaking. Further, the changes in the functional groups identified by Fourier-transform infrared spectroscopy analysis and the changes in the surface morphology of the pulp fibers were obtained using scanning electron microscope analysis. [Display omitted] • The microbial cellulase enzyme produced was effective in the deinking process. • Bacillus wiedmannii was molecularly characterized, it generated 0.0591U/ml cellulase enzyme. • This work demonstrated that 3% of paper pulp could be handled with a 20% enzyme dose. • Bio-deinking is a new and unexplored method with a promising future. [ABSTRACT FROM AUTHOR]

This work deals with the performance of a microbial fuel cell, focusing on the electrocatalytic activity of selected cathodes constructed by coating nanocomposites over graphite felt under neutral pH in a doublechamber configuration using paper-recycled waste water as a typical electrolyte. Among all cathodes, iron phthalocyanine (FePc) combined multiwalled carbon nanotubes (MWCNT) shows the highest power density (9.34 W/m2) compared to other two catalysts, FePc/Ketjan black (4.68 W/m2) and MWCNT (2.9 W/m2) under similar conditions of using a reference platinum/carbon (Pt/C) loading of 0.5 mg/cm2. The morphology of these catalyst coated electrodes was characterized by scanning electron microscopy. Their electrocatalytic activities were examined using cyclic voltammetry. This work provides an appropriate alternative for cathode catalysts in treatment as well as in electricity production as demonstrated by the high power density of the above catalysts compared to that using precious Pt metal catalyst in microbial fuel cells. [ABSTRACT FROM AUTHOR]

The Fe-N-C nanofibers (NFs) exhibit excellent electro-catalytic activity for oxygen reduction reaction (ORR), which is essential for energy conversion system. Compared with the traditional ink-based electrode, we synthesized the structured Fe-N-C ANFs/CP (activated NFs derived from polypyrrole(PPy) doped with iron atoms in situ grown on carbon paper) by electrochemical polymerization. Herein, we investigate the effect of the iron concentration on the electro-catalytic activity for ORR, revealing that the as-prepared 0.05-Fe-N-C ANFs exhibit superior electro-catalytic activity than 0.01-Fe-N-C ANFs, 0.03-Fe-N-C ANFs as well as 0.10-Fe-N-C ANFs and excellent durability in alkaline solution. It is shown that the better electro-catalytic activity of 0.05-Fe-N-C ANFs for ORR could be ascribing to the fluffy fibrous structure, higher Fe-Nx concentration, and well-dispersed catalytic active sites. [ABSTRACT FROM AUTHOR]

Translating to the Community (T2C) is a social biorepository designed to advance new diagnostic tools and realign community-clinical processes, with the aim to mitigate the short- and long-term impacts of fetal alcohol spectrum disorder (FASD) as well as prenatal alcohol exposure and its co-morbidities and behaviors. In this paper, we describe the evolution of this repository as a new translational partnership to advance a precision-medicine approach to FASD. Key to its evolution was a partnership between academic researchers, Indigenous communities, families, and a regional diagnostic clinic. We further describe the rationale for social biobanking, the type of banking, ethical engagement of families, communities, and clinics, their roles in repository design, governance, translation, and research activities, types of data collected from families, and how the study data are managed, reported, and accessed. The repository design includes biological samples, social-contextual health-survey data, and clinical data (which are linkable to administrative data) from community and clinical cohorts of diagnosed children, children prenatally exposed but not diagnosed, children suspected to have had a prenatal exposure, and related siblings, biological parents, and unrelated children and their parents. From these cohorts and families, potential studies drawing on this data will shed light on various risk factors, social and biological pathways, and service utilization issues, with the aim to implement primary and secondary prevention and intervention strategies. [ABSTRACT FROM AUTHOR]

Urgent need for waste disposal and renewable energy have opened up promising pathways for renewable and sustainable fuel production to substitute traditional fossil fuels. In this study, catalytic co-pyrolysis of waste paper (WP) and polyvinyl chloride (PVC) as typical municipal solid wastes was experimentally investigated towards hydrogen-rich syngas production. Results indicated the maximum H 2 yield (429 μmol·g cat −1·min−1) was obtained with 60% PVC weight ratio under 900 °C which was higher than single component pyrolysis. Higher hydrogen yield (681.76 μmol·g cat −1·min−1) appeared over Fe/CeO 2 –CaO under the optimal conditions compared to that of Ru/ZSM-5-CaO (445.54 μmol·g cat −1·min−1). From the calculated non-isothermal kinetic parameters, both catalysts could reduce activation energies. Proper porous structure and CaO content in the catalyst could enhance hydrogen production via carbon species fixation. • Catalytic co-pyrolysis of waste paper and PVC blends for hydrogen production is firstly investigated. • Enhanced interactions of PVC/waste paper during pyrolysis was found for H 2 production. • Non-isothermal kinetics were implemented to evaluate catalytic co-pyrolysis. • High H 2 yield was obtained over Fe/CeO 2 –CaO for its pore structure and sorption enhancing effect. [ABSTRACT FROM AUTHOR]

Co(salen) powders were homogeneously scattered over a ceramic fibre network to give a catalyst paper and the Co(salen) paper was tested for the oxidative degradation of a kraft lignin using H2O2 as an oxidant. Due to the structural effect of the interconnected 3D-network, the catalyst paper exhibited a higher performance in the oxidation of kraft lignin with a oil yield of 23.27 % than the original Co(salen) powder with an oil yield of 10.63 %, along with excellent recycling performance. 2,6-Dimethoxyphenol (2.32 mg/kg kraft lignin), vanillin (3.80 mg/kg kraft lignin), and syringaldehyde (2.63 mg/kg kraft lignin) were found to be the main products in the oil obtained. In addition, the structural changes in the kraft lignin were also studied during the process. The phenolic compounds were formed through side chain oxidation together with the oxidative cleavage of α-O-4 linkage. [ABSTRACT FROM AUTHOR]

A core-shell catalyst supported on the carbon fiber paper was developed for the effective electrocatalytic reduction of concentrated nitric acid (4.0 M). The potential range of cyclic voltammetry deposition was adjusted to investigate the influence of the chemical state of electrodeposited Ir on concentrated nitric acid reduction. The results indicate that a core of Pt with a thin IrO 2 shell shows greatly enhanced catalytic activity comparing to the nano-Pt. A Pt@IrO 2 core-shell catalyst was synthesized by a two-step cyclic voltammetry. It shows a high reactivity toward electrocatalytic reduction of concentrated nitric acid (4.0 M). Unlabelled Image • The Pt core with Ir shell catalyst was designed for the effective nitric acid reduction. • The chemical state of Ir shell plays an important role in the reduction process. • The Pt@IrO 2 /CFP electrode shows a higher current density than that of Pt@Ir/CFP. [ABSTRACT FROM AUTHOR]

Volatile organic compounds (VOCs) are a significant source of environmental pollution, posing threats to human safety. With growing concerns about environmental degradation, catalytic oxidation technology emerges as a paramount and widely adopted approach for VOC elimination, renowned for its operational simplicity, energy efficiency, and environmental friendliness. As a representative transition metal catalyst, cobalt‐based catalysts have garnered widespread use in VOC catalytic oxidation due to their cost‐effectiveness, versatility, and distinctive physicochemical properties. This paper provides a detailed exposition of the construction strategies and structure‐activity relationship of Co3O4‐based catalysts in VOCs oxidation reaction, encompassing both monometallic Co3O4 and multimetallic cobalt‐based catalysts. Furthermore, it offers a comprehensive summary and discussion of the latest research progress concerning Co3O4‐based catalysts in practical applications. Concluding with a meticulous analysis, the paper addresses the technical challenges inherent in developing Co3O4‐based catalysts for VOCs degradation. Additionally, it proposes research directions aimed at overcoming these challenges, contributing to the ongoing discourse on environmental sustainability. [ABSTRACT FROM AUTHOR]

The aviation ecosystem is increasingly coming under pressure to decarbonise from the public and governments. Airports are at the leading edge of transforming their operations, alongside airlines and aerospace companies. While, however, the levers to reduce Scope 1 and 2 airport emissions are well understood, how to address Scope 3 emissions (which account for the bulk of an airport's emissions) remains a major challenge. This paper provides an overview of potential Scope 3 decarbonisation levers across aircraft operations, ground transport and infrastructure construction. The paper then assesses the potential impact on emissions, and ease of implementation of these levers, highlighting aircraft operations as the area with highest potential to reduce ecosystem emissions. Next, the paper looks at how some of these levers have been implemented in practice, based on the case study of Geneva Airport, focusing on supporting sustainable mobility, energy support for aircraft and financial incentives for airlines to use latest-generation aircraft. The paper then identifies and discusses key barriers that must be overcome, including the ability of airports to influence domains outside their direct control, competing governmental policies and need for investment, highlighting the need for collaboration between a wide range of stakeholders. Based on this, the paper suggests a number of actions that airports should take to satisfy stakeholders and catalyse the aviation ecosystem towards its goal of achieving net zero. [ABSTRACT FROM AUTHOR]

In order to realize the intelligent recognition and statistics of hydrogenation catalyst image information, this paper presents a new method to judge the active phase by image recognition, which is different from traditional methods. Firstly, considering that hydrogenation catalyst image targets are small and easy to stack, the feature extraction network in the CenterNet model is optimized by adding the multi-feature fusion module to improve the accuracy of the network in edge positioning. Secondly, according to the linear shape of the hydrogenation catalyst, the mask branch is added to the CenterNet model to train the hydrogenation catalyst stripes with unclear target to reduce the leakage rate of the hydrogenation catalyst. The experimental results show that the detection accuracy of the improved CenterNet network is 91 % , 7 % higher than that of the original one, with a decline in detection rate by 12 % . The method proposed in this paper can accurately identify and segment the hydrogenation catalyst in the electron microscope image, which can provide technical support for the statistics and analysis of the hydrogenation catalyst image. [ABSTRACT FROM AUTHOR]

The increasing environmental consideration and the growth of instability of the energy market call for methods that can process the organic fraction of municipal solid waste (OFMSW) into fuel instead of disposal. Due to the pyrolysis and gasification that are efficient procedures to achieve valuable products, gasification of OFMSW with different particle sizes and compositions was carried out in the presence of Ni and Ni-Ce-loaded Y-zeolite in a multizone tubular kiln reactor. During the experiments, 500°C was applied in the first reactor zone, while the 2nd zone was at an elevated temperature of 600°C or 900°C in the presence of steam. The combined pyrolysis and gasification experiments were also carried out without a catalyst with the same operating conditions. The feedstock was collected from the organic fraction of a Hungarian mechanical-biological treatment (MBT) plant and was separated into four different fractions based on particle size: <1 cm dry biomass and fine particles, 1-2 cm paper-rich, 2-6 cm paper and plastic-rich feedstocks, and <6 cm mixture of these fractions. During the experimental work, product yields; gaseous product composition; the ratio of H2/CO, CO2/CO, and CH4/CO; and lower heating value were determined in the function of feedstock composition, the applied temperature, and catalysts. It was found that the hydrogen content and H2/CO ratio of gaseous products were increased due to catalyst application and temperature elevation in the 2nd reactor zone. The addition of Ce to the Ni/Y-zeolite catalyst was advantageous in the case of hydrogen formation at a lower temperature (600°C). The hydrogen and methane content of products obtained from the catalytic pyrolysis-gasification of paper and plastic-rich OFMSWs on elevated temperatures were higher, which increased the lower heating value of those products. Based on the elemental analysis of the obtained solid residues, it was found that paper/plastic-rich feedstock released hydrogen and carbon with a higher extent. 1-2 cm feedstock-related solid residues had the highest H/C ratio which caused a 12.5-12.8 MJ/kg gross heating value. As a result, combined pyrolysis and gasification appear to be an efficient method to attain valuable outputs from OFMSW not only in gas but also in solid products. [ABSTRACT FROM AUTHOR]

Direct internal reforming (DIR) operation of a solid oxide fuel cell (SOFC) is a very attractive concept for downsizing and cost reduction of SOFC systems. This study aimed to develop stable operation of a DIR-SOFC fuelled by biogas. The current-voltage (I-V) curves of 2 × 2 cm 2 planar SOFCs (anode- and electrolyte-supported cells, ASC and ESC, respectively.) were measured at 800 °C in the direct feed of a simulated biogas mixture (CH 4 /CO 2 = 1), and the flexible structured catalyst material (paper-structured catalyst (PSC)) was applied on the anode material for performance enhancement. By applying a hydrotalcite (HT)-dispersed PSC (HT-PSC), the sulfur tolerance of the SOFC in the DIR operation was remarkably improved. By the effect of the HT-PSC, for both ASC and ESC, a stable cell voltage higher than 800 mV was obtained over 200 h at 0.2 A cm −2 in the direct feed of simulated biogas under 5 ppm H 2 S poisoning. [ABSTRACT FROM AUTHOR]

By exploiting the hydrophilicity of cellulose filter paper (FP) and the excellent chelating property of chitosan (CH) for Mn2+, we have designed an efficient and retrievable dip catalyst MnO 2 /CH-FP for Fenton-like degradation of methylene blue (MB) over a wide pH range from 2.8 to 11.2. The MnO 2 nanoparticles were uniformly immobilized in the CH-FP matrix by in-situ redox precipitation method where Mn(NO 3) 2 was treated with KMnO 4 at mild conditions. A series of MnO 2 /CH-FP hybrids with different MnO 2 loading were fabricated via varying concentration of Mn(NO 3) 2 solution, and their structure-function relationships were discussed based on detailed characterization. The optimal catalyst 1.0MnO 2 /CH-FP could cooperate with multiple low-concentration dosages of H 2 O 2 to efficiently degrade 95.6% MB in 90 min (50 mg L−1 MB, 1 g L−1 catalyst, 30 mg L−1 H 2 O 2 , pH 7). It is also shown that 1.0MnO 2 /CH-FP could still keep 83.3% degradation efficiency of MB after six cycles. Moreover, the activity of this composite greatly surpassed that of bare MnO 2 for nearly 50%, owing to its larger surface area and more accessible active sites. This method for preparing MnO 2 /CH-FP could effectively avoid the agglomeration of MnO 2 nanoparticles and make the reaction turn on/off almost instantaneously by mere insertion/removal. Image 1 • Nano-MnO 2 was in-situ anchored on the biopolymer by redox precipitation method. • It was an efficient and highly retrievable dip catalyst for Fenton-like degradation. • The hybrid has lager surface area and more accessible active sites than bare MnO 2. • The relationship between MnO 2 loading and degradation efficiency was discussed. • Multiple low-concentration doses of H 2 O 2 could achieve better decolorization. [ABSTRACT FROM AUTHOR]

Highly efficient and durable anode electrocatalysts are the key to boost the performance of direct organic-molecule fuel cells (DOMFCs), yet there are still many challenges need to be solved. The PdPt alloy nanocrystals have been regarded as the most promising anode catalysts of DOMFCs, and the further improvement of their catalytic performance has attracted much attention. The effective routes includes tailoring the surface structure and optimizing the alloy composition of PdPt nanocatalysts. The high-index faceted structures possess high density of terraces and atomic steps which are efficient for electrooxidation reactions of small organic-molecule fuels, such as formic acid and ethanol. In particular, electrochemically-controlled synthesis methods present unique advantages in achieving such high-index faceted nanostructures. The current paper reports a direct electrodeposition of PdPt concave nanocubes on carbon paper (denoted as PdPt-CNC/CP). The prepared PdPt-CNC/CP has high-index faceted surface structures varying from {610} to {830}. When served as electrocatalysts, the PdPt-CNC/CP brings in outstanding mass specific activity and durability towards both formic acid oxidation reaction (FAOR) and ethanol oxidation reaction (EOR). More importantly, the selectivity of complete oxidation pathway through the cleavage of C-C bond on PdPt-CNC/CP during EOR in alkaline solution has been confirmed through NMR analysis. Based on the convenient method of direct electrodeposition of PdPt concave nanocubes on carbon paper and their excellent catalytic activity and durability, the PdPt-CNC/CP catalysts have potential advantages in being used as catalyst layers directly for membrane electrode assembly (MEA) in fuel cells, due to the reduced catalyst loading and simplified assembly process in comparison with traditional preparation procedure. Image 1 [ABSTRACT FROM AUTHOR]

In recent years, the catalyst efficiency of hydrogen evolution reaction (HER) has been extensively studied. However, the stability of catalysts at high current densities is still a challenge. Herein, layered Ni−Co−P was electrodeposited on carbon fiber paper (CFP) via cyclic voltammetry (CV). This low‐cost electrode exhibits high efficiency and excellent durability for HER in 1 M KOH. To achieve current densities of 10, 100, 500, and 1000 mA cm−2, Ni−Co−P/CFP required overpotentials of 49, 95, 170, and 295 mV, respectively. The layered structure allows the catalyst to fall off layer by layer. After the outer layer of catalyst falls off, the inner layer of catalyst will be exposed to continue working. After 300 h of HER at 1000 mA cm−2, Ni−Co−P/CFP still has a regular morphology and high efficiency. Our work shows that layered Ni−Co−P/CFP has excellent prospects for practical applications. [ABSTRACT FROM AUTHOR]

A scalable, and cost-effective method was employed to prepare self-supported CuSn bimetallic catalyst on carbon paper. The obtained CuSn catalyst demonstrates high faradaic efficiency of CO around or above 90% at a broad potential range from −0.7 to −1.8 V vs. reversible hydrogen electrode, greatly surpassing Cu or Sn counterparts. [ABSTRACT FROM AUTHOR]