Tuning the Metal-Support Interaction by Modulating CeO2 Oxygen Vacancies to Enhance the Toluene Oxidation Activity of Pt/CeO2 Catalysts.

In this research, a range of Pt/CeO2 catalysts featuring varying Pt-O-Ce bond contents were developed by modulating the oxygen vacancies of the CeO2 support for toluene abatement. The Pt/CeO2-HA catalyst generated a maximum quantity of Pt-O-Ce bonds (possessed the strongest metal-support interaction), as evidenced by the visible Raman results, which demonstrated outstanding toluene catalytic performance. Additionally, the UV Raman results revealed that the strong metal-support interaction stimulated a substantial increase in oxygen vacancies, which could facilitate the activation of gaseous oxygen to generate abundant reactive oxygen species accumulated on the Pt/CeO2-HA catalyst surface, a conclusion supported by the H2-TPR, XPS, and toluene-TPSR results. Furthermore, the results from quasi-in situ XPS, in situ DRIFTS, and DFT indicated that the Pt/CeO2-HA catalyst with a strong metal-support interaction led to improved mobility of reactive oxygen species and lower oxygen activation energies, which could transfer a large number of activated reactive oxygen species to the reaction interface to participate in the toluene oxidation, resulting in the relatively superior catalytic performance. The approach of tuning the metal-support interaction of catalysts offers a promising avenue to develop highly active catalysts for toluene degradation.

Derivatives of Br-doped metal-organic framework for improved acetaldehyde adsorption-photocatalytic oxidation.

Different Br-doped metal-organic frameworks (MOFs) derived (Brx@UiO-66) have been prepared by heat treatment using UiO-66 as the precursor. The experimental results showed that Br0.2@UiO-66 exhibited the best photocatalytic oxidation and adsorption performances toward acetaldehyde. In the dynamic system, the acetaldehyde removal rate and adsorption capacity of Br0.2@UiO-66 were 93.2 % and 230.59 mg/g, respectively. The improvement of the photocatalytic performance can be attributed to the presence of Br ions and CBr bonds, which facilitated the rapid separation of electrons and holes and the production of •O2-. In addition, Br0.2@UiO-66 had a better adsorption performance than 300UiO-66, mainly because of the increased Lewis acidity of the metal active sites due to Br doping. Radical capture experiments indicated that •O2- and e- were the primary active substances in acetaldehyde oxidation, and allowed establishing the possible mechanism of acetaldehyde oxidation. This work shows that MOFs can have high catalytic oxidation performances toward volatile organic compounds (VOCs) while retaining their adsorption capacity, and can be used for practical applications in the adsorption-catalytic integrated degradation of VOCs.

Low-temperature NH3 abatement via selective oxidation over a supported copper catalyst with high Cu+ abundance.

Selective catalytic NH3-to-N2 oxidation (NH3-SCO) is highly promising for abating NH3 emissions slipped from stationary flue gas after-treatment devices. Its practical application, however, is limited by the non-availability of low-cost catalysts with high activity and N2 selectivity. Here, using defect-rich nitrogen-doped carbon nanotubes (NCNT-AW) as the support, we developed a highly active and durable copper-based NH3-SCO catalyst with a high abundance of cuprous (Cu+) sites. The obtained Cu/NCNT-AW catalyst demonstrated outstanding activity with a T50 (i.e. the temperature to reach 50% NH3 conversion) of 174°C in the NH3-SCO reaction, which outperformed not only the Cu catalyst supported on N-free O-functionalized CNTs (OCNTs) or NCNT with less surface defects, but also those most active Cu catalysts in open literature. Reaction kinetics measurements and temperature-programmed surface reactions using NH3 as a probe molecule revealed that the NH3-SCO reaction on Cu/NCNT-AW follows an internal selective catalytic reaction (i-SCR) route involving nitric oxide (NO) as a key intermediate. According to mechanistic investigations by X-ray photoelectron spectroscopy, Raman spectroscopy, and X-ray absorption spectroscopy, the superior NH3-SCO performance of Cu/NCNT-AW originated from a synergy of surface defects and N-dopants. Specifically, surface defects promoted the anchoring of CuO nanoparticles on N-containing sites and, thereby, enabled efficient electron transfer from N to CuO, increasing significantly the fraction of SCR-active Cu+ sites in the catalyst. This study puts forward a new idea for manipulating and utilizing the interplay of defects and N-dopants on carbon surfaces to fabricate Cu+-rich Cu catalysts for efficient abatement of slip NH3 emissions via selective oxidation.

Investigation of catalytic methane oxidation over Ag/Co2MOx (M = Co, Ni, Cu) catalysts with varying interfacial electron transfer.

Atom-doped Co3O4 catalysts loaded with Ag were examined as cost-effective catalysts for methane oxidation. The synthesized Ag/Co2NiOx catalysts exhibited distinctive surface characteristics in contrast with Ag/Co3O4 and Ag/Co2CuOx catalysts prepared using a similar method. Characterization results unveiled that Ag/Co2NiOx featured a higher presence of active surface oxygen species, lattice defects, a larger surface area, and enhanced reducibility. A methane oxidation catalytic performance followed the sequence: Ag/Co2NiOx > Ag/Co3O4 > Ag/Co2CuOx. The investigation delved into methane degradation pathways on the surfaces of three catalysts, examining their behavior under both aerobic and anaerobic atmospheres through in-situ DRIFTS analysis. Furthermore, introducing Ag showed a marked positive effect on Co-Ni mixed oxide, inducing electron transfer and a more active electron system, whereas it exhibited an inverse impact within the surface of Co-Cu mixed oxide. This work provides innovative perspectives on the development of forthcoming environmental catalysts.

Enhancement Effect Induced by the Second Metal to Promote Ozone Catalytic Oxidation of VOCs.

It is a promising research direction to develop catalysts with high stability and ozone utilization for low-temperature ozone catalytic oxidation of VOCs. While bimetallic catalysts exhibit excellent catalytic activity compared with conventional single noble metal catalysts, limited success has been achieved in the influence of the bimetallic effect on the stability and ozone utilization of metal catalysts. Herein, it is necessary to systematically study the enhancement effect in the ozone catalytic reaction induced by the second metal. With a simple continuous impregnation method, a platinum-cerium bimetallic catalyst is prepared. Also highlighted are studies from several aspects of the contribution of the second metal (Ce) to the stability and ozone utilization of the catalysts, including the "electronic effect" and "geometric effect". The synergistic removal rate of toluene and ozone is nearly 100% at 30 °C, and it still shows positive stability after high humidity and a long reaction time. More importantly, the instructive significance, which is the in-depth knowledge of enhanced catalytic mechanism of bimetallic catalysts resulting from a second metal, is provided by this work.

Tuning the Hierarchical Pore Structure and the Metal Site in a Metal-Organic Framework Derivative to Unravel the Mechanism for the Adsorption of Different Volatile Organic Compounds.

Volatile organic compounds (VOCs) are one of the main classes of air pollutants, and it is important to develop efficient adsorbents to remove them from the atmosphere. To do this most efficiently, we need to understand the mechanism of VOC adsorption. In this work, we described how the metal organic framework (MOF), ZIF-8, was used as a precursor to generate MOF derivatives (Zn-GC) through temperature-controlled calcination, which had adjustable metal sites and hierarchical pore structure. It was used as a model adsorbent to study the adsorption and desorption characteristics of different VOCs. Zn-GC-850 with developed pores exhibited higher adsorption performance for the benzene series, whereas Zn-GC-650 with more metal sites had a better adsorption capacity for oxygen-containing VOCs. By tuning the molecular structure of the VOCs, we revealed the adsorption mechanism of different VOCs at the molecular level. The more developed hierarchical pore structure obtained at the higher temperature facilitates the diffusion of the benzene series, and the noncovalent interaction between their methyl group(s) and the carbonized MOF derivatives improves the adsorption affinity; while the higher exposure of Zn sites obtained at lower temperature favors the adsorption of oxygen-containing VOCs by Zn-O bonds. The mass transfers of VOCs and the role of the adsorbent were simulated by multiple theoretical models. This study strengthens the basis for the design and optimization of the adsorbent and catalyst for VOCs treatment.

Generation Characteristics of Solid Byproducts of the C4F7N-CO2-O2 Gas Mixture under PD Fault.

With the gradual improvement of the requirements for the safe and stable operation of gas-insulated equipment (GIE), the eco-friendly insulating gas C4F7N-CO2-O2 has become the best choice to replace SF6 and apply it to various medium-voltage (MV) and high-voltage (HV) GIE. At present, the generation characteristics of solid decomposition products of the C4F7N-CO2-O2 gas mixture under partial discharge (PD) fault need to be studied. In this paper, a 96 h PD decomposition test was carried out by simulating metal protrusion defects in GIE with needle-plate electrodes to study the generation characteristics of C4F7N-CO2-O2 gas mixture solid decomposition products under PD fault and their compatibility with metal conductors. It was found that obvious ring-shaped solid precipitates appeared in the central area of the surface of the plate electrode under the action of long-term PD, mainly including metal oxides (CuO), silicates (CuSiO3), fluorides (CuF, CFX), carbon oxides (CO, CO2), and nitrogen oxides (NO, NO2). The addition of 4% O2 has little effect on the element composition and valence state of PD solid precipitates, but it can reduce their yield to a certain extent. The corrosion effect of O2 in the gas mixture on metal conductors is weaker than that of C4F7N.

Space Charge Characteristics at the Interface of Laminated Epoxy Resin.

In the design and manufacturing of epoxy resin insulation components, complex structures can be achieved through multiple pours, thereby forming the structure of interface of laminated epoxy resin. This type of interface structure is often considered a weak link in performance which can easily accumulate charges and cause electric field distortion. However, research on the interlayer interface of epoxy resin has received little attention. In this study, epoxy samples with and without interlayer interfaces were prepared, and the space charge accumulation characteristics and trap characteristics of the samples were analyzed via pulsed electro-acoustic (PEA) and thermally stimulated depolarization current (TSDC) methods. The experimental results indicate that the Maxwell-Wagner interface polarization model cannot fully explain the charge accumulation at the interface. Due to the influence of the secondary curing, the functional groups in the post-curing epoxy resin can move and react with the partially reacted functional groups in the prefabricated epoxy resin layer, resulting in a weak cross-linking network at the interface. With the increase in temperature, the molecular chain segments in the weak cross-linked region of the interface become more active and introduce deep traps at the interface, thereby exacerbating the accumulation of interface charges. In addition, due to the influence of interface polarization and weak cross-linking, the ability of the interface charges to cause field strength distortions decreases with the increase in applied field strength. This research study can provide a theoretical reference for the interfacial space charge transport characteristics of epoxy-cured cross-linked layers and provide ideas for regulating interfacial cross-linking to suppress interfacial charge accumulation.

Synthesis of xCe-MnO2 with three-dimensional ultra-thin nanosheet structure and its excellent low-temperature reducibility for toluene catalysis.

A series of xCe-MnO2 (x = 0-1) catalysts were synthesized using ammonium oxalate as a precipitator via the redox precipitation method and hydrothermal synthesis method. The results indicate that 0.25Ce-MnO2 exhibited the highest catalytic activity for toluene oxidation, with the T99 of 240 °C. Characterization results from XRD, Raman, SEM, TEM, EDS-mapping, BET, and other techniques reveal that the 0.25Ce-MnO2 catalyst exhibited a three-dimensional multistage ultrathin nanosheet structure by adjusting the introduction amount of Ce, with abundant active sites, and effectively formed Ce-Mn homogeneous dispersion. The larger pore size and volume of 0.25Ce-MnO2 catalyst lead to it excellent toluene transfer ability. Furthermore, compared with MnO2, the crystal pattern of 0.25Ce-MnO2 shifted to the tetragonal cryptomelane type α-MnO2 phase and exposed more crystal planes which are beneficial to catalyze toluene. H2-TPR, O2-TPD, and XPS characterization further confirmed the strong interaction between Ce and Mn oxides, which exhibited better low-temperature reducibility and oxygen migration, along with abundant Ce3+ and Mn3+ species, where lattice oxygen played a major role. Moreover, in situ DRIFTS revealed that the 0.25Ce-MnO2 catalyst showed higher adsorption and desorption capacity for toluene than the MnO2 catalyst, and benzoate species were the key intermediates for catalytic oxidation. Additionally, benzoate and surface phenolic species were the key intermediates for catalytic oxidation of MnO2. Because 0.25Ce-MnO2 possesses better ability of converting toluene to benzoate species, it exhibits better activity.

Electrospun Ce-Mn oxide as an efficient catalyst for soot combustion: Ce-Mn synergy, soot-catalyst contact, and catalytic oxidation mechanism.

Increasing the contact efficiency and improving the intrinsic activity are two effective strategies to obtain efficient catalysts for soot combustion. Herein, the electrospinning method is used to synthesize fiber-like Ce-Mn oxide with a strong synergistic effect. The slow combustion of PVP in precursors and highly soluble manganese acetate in spinning solution facilitates the formation of fibrous Ce-Mn oxides. The fluid simulation clearly indicates that the slender and uniform fibers provide more interwoven macropores to capture soot particles than the cubes and spheres do. Accordingly, electrospun Ce-Mn oxide exhibits better catalytic activity than reference catalysts, including Ce-Mn oxides by co-precipitation and sol-gel methods. The characterizations suggest that Mn3+ substitution into fluorite-type CeO2 enhances the reducibility through the acceleration of Mn-Ce electron transfer, improves the lattice oxygen mobility by weakening the Ce-O bonds, and induces oxygen vacancies for the activation of O2. The theoretical calculation reveals that the release of lattice oxygen becomes easy because of a low formation energy of oxygen vacancy, while the high reduction potential is beneficial for the activation of O2 on Ce3+-Ov (oxygen vacancies). Due to above Ce-Mn synergy, the CeMnOx-ES shows more active oxygen species and higher oxygen storage capacity than CeO2-ES and MnOx-ES. The theoretical calculation and experimental results suggest that the adsorbed O2 is more active than lattice oxygen and the catalytic oxidation mainly follows the Langmuir-Hinshelwood mechanism. This study indicates that electrospinning is a novel method to obtain efficient Ce-Mn oxide.

Scalable Fabrication of Superhydrophobic Coating with Rough Coral Reef-Like Structures for Efficient Self-Cleaning and Oil-Water Separation: An Experimental and Molecular Dynamics Simulation Study.

Superhydrophobic coating has a great application prospect in self-cleaning and oil-water separation but remains challenging for large-scale preparation of robust and weather-resistant superhydrophobic coatings via facile approaches. Herein, this work reports a scalable fabrication of weather-resistant superhydrophobic coating with multiscale rough coral reef-like structures by spraying the suspension containing superhydrophobic silica nanoparticles and industrial coating varnish on various substrates. The coral reef-like structures effectively improves the surface roughness and abrasion resistance. Rapid aging experiments (3000 h) and the outdoor building project application (3000 m2 ) show that the sprayed superhydrophobic coating exhibits excellent self-cleaning properties, weather resistance, and environmental adaptability. Moreover, the combined silica-coating varnish-polyurethane (CSCP) superhydrophobic sponge exhibits exceptional oil-water separation capabilities, selectively absorbing the oils from water up to 39 times of its own weight. Furthermore, the molecular dynamics (MD) simulation reveals that the combined effect of higher surface roughness, smaller diffusion coefficient of water molecules, and weaker electrostatic interactions between water and the surface jointly determines the superhydrophobicity of the prepared coating. This work deepens the understanding of the anti-wetting mechanism of superhydrophobic surfaces from the perspective of energetic and kinetic properties, thereby paving the way for the rational design of superhydrophobic materials and their large-scale applications.

Unraveling the role of Co3O4 facet for photothermal catalytic oxidation of methanol via operando spectroscopy and theoretical investigation.

Tubular, pie- and bread-shaped forms of Co3O4 with exposed {110}, {112} and {111} facets were prepared and compared in their photothermal catalytic performance and reaction pathways during the oxidation of methanol. Among them, the Co3O4 with exposed {110} facet exhibited the best photothermal catalytic performance (95% methanol conversion, 93% CO2 yield) under solar irradiation, while also maintaining good stability and moisture resistance. Reaction mechanism studies showed that the {110} facets had a strong adsorption capacity for formaldehyde, which facilitated its conversion to formate. The transformation of formaldehyde to formate species was the key step. The key step on the {110} facet was conversion of formaldehyde to a mono-dentate formate species, while conversion on the {112} and {111} facets was mainly to bi-dentate formate species. This study demonstrated that the design of preferential exposed crystal facet can regulate the pathway of photothermal catalytic reaction and realize efficient solar energy utilization.

Compatibility and Interaction Mechanism between the C4F7N/CO2/O2 Gas Mixture and FKM and NBR.

The C4F7N/CO2/O2 gas mixture received a great deal of attention for its potential use in eco-friendly gas-insulated equipment (GIE). The evaluation of the compatibility between C4F7N/CO2/O2 and sealing rubber is necessary and significant considering the high working pressure (0.14-0.6 MPa) of GIE. Herein, we explored the compatibility between C4F7N/CO2/O2 and fluororubber (FKM) and nitrile butadiene rubber (NBR) for the first time by analyzing the gas components, rubber morphology, elemental composition, and mechanical properties. The interaction mechanism of the gas-rubber interface was further investigated based on the density functional theory. We found that C4F7N/CO2/O2 is compatible with FKM and NBR at 85 °C, while the surface morphology changed at 100 °C, with white granular and agglomerated lumps appearing on FKM and multi-layer flakes being generated on NBR. The accumulation of the fluorine element occurred, and the compressive mechanical properties of NBR deteriorated after the gas-solid rubber interaction. Overall, the compatibility between FKM and C4F7N/CO2/O2 is superior, which could be employed as the sealing material for C4F7N-based GIE.

Insights into the Role of Nanorod-Shaped MnO2 and CeO2 in a Plasma Catalysis System for Methanol Oxidation.

Published papers highlight the roles of the catalysts in plasma catalysis systems, and it is essential to provide deep insight into the mechanism of the reaction. In this work, a coaxial dielectric barrier discharge (DBD) reactor packed with γ-MnO2 and CeO2 with similar nanorod morphologies and particle sizes was used for methanol oxidation at atmospheric pressure and room temperature. The experimental results showed that both γ-MnO2 and CeO2 exhibited good performance in methanol conversion (up to 100%), but the CO2 selectivity of CeO2 (up to 59.3%) was much higher than that of γ-MnO2 (up to 28.6%). Catalyst characterization results indicated that CeO2 contained more surface-active oxygen species, adsorbed more methanol and utilized more plasma-induced active species than γ-MnO2. In addition, in situ Raman spectroscopy and Fourier transform infrared spectroscopy (FT-IR) were applied with a novel in situ cell to reveal the major factors affecting the catalytic performance in methanol oxidation. More reactive oxygen species (O22-, O2-) from ozone decomposition were produced on CeO2 compared with γ-MnO2, and less of the intermediate product formate accumulated on the CeO2. The combined results showed that CeO2 was a more effective catalyst than γ-MnO2 for methanol oxidation in the plasma catalysis system.

Quenching-Induced Defect-Rich Platinum/Metal Oxide Catalysts Promote Catalytic Oxidation.

Enhancing oxygen activation through defect engineering is an effective strategy for boosting catalytic oxidation performance. Herein, we demonstrate that quenching is an effective strategy for preparing defect-rich Pt/metal oxide catalysts with superior catalytic oxidation activity. As a proof of concept, quenching of α-Fe2O3 in aqueous Pt(NO3)2 solution yielded a catalyst containing Pt single atoms and clusters over defect-rich α-Fe2O3 (Pt/Fe2O3-Q), which possessed state-of-the-art activity for toluene oxidation. Structural and spectroscopic analyses established that the quenching process created abundant lattice defects and lattice dislocations in the α-Fe2O3 support, and stronger electronic interactions between Pt species and Fe2O3 promote the generation of higher oxidation Pt species to modulate the adsorption/desorption behavior of reactants. In situ diffuse reflectance infrared Fourier transform spectroscopy (in situ DRIFTS) characterization studies and density functional theory (DFT) calculations determined that molecular oxygen and Fe2O3 lattice oxygen were both activated on the Pt/Fe2O3-Q catalyst. Pt/CoMn2O4, Pt/MnO2, and Pt/LaFeO3 catalysts synthesized by the quenching method also offered superior catalytic activity for toluene oxidation. Results encourage the wider use of quenching for the preparation of highly active oxidation catalysts.

Spatiotemporal analysis and prediction of water quality in Pearl River, China, using multivariate statistical techniques and data-driven model.

Identifying spatiotemporal variation patterns and predicting future water quality are critical for rational and effective surface water management. In this study, an exploratory analysis and forecast workflow for water quality in Pearl River, Guangzhou, China, was established based on the 4-h interval dataset selected from 10 stations for water quality monitoring from 2019 to 2021. The multiple statistical techniques, such as cluster analysis (CA), principal component analysis (PCA), correlation analysis (CoA), and redundancy analysis (RDA), as well as data-driven model (i.e., gated recurrent unit (GRU)), were applied for assessing and predicting the water quality in the basin. The investigated sampling stations were classified into 3 categories based on differences in water quality, i.e., low, moderate, and high pollution regions. The average water quality indexes (WQI) values ranged from 38.43 to 92.63. Nitrogen was the most dominant pollutant, with high TN concentrations of 0.81-7.67 mg/L. Surface runoff, atmospheric deposition, and anthropogenic activities were the major contributors affecting the spatiotemporal variations in water quality. The decline in river water quality during the wet season was mainly attributed to increased surface runoff and extensive human activities. Furthermore, the short-term prediction of river water quality was achieved using the GRU model. The result indicated that for both DLCK and DTJ stations, the WQI for the 5-day lead time were predicted with accuracies of 0.82; for the LXH station, the WQI for the 3-day lead time was forecasted with an accuracy of 0.83. The finding of this study will shed a light on an effective reference and systematic support for spatio-seasonal variation and prediction patterns of water quality.

Surface adsorbed and lattice oxygen activated by the CeO2/Co3O4 interface for enhancive catalytic soot combustion: Experimental and theoretical investigations.

Metal oxide-oxide interface on supported catalyst has been rarely studied due to the complex interfacial structure and synthetic challenge. Herein, different Ag-supported CeO2/Co3O4 samples with various covered-state of CeO2 were prepared for catalytic soot oxidation. In comparison, catalytic activity was significantly improved by grafting CeO2 on Co3O4, in which the best performing Ag/CoCe-2 exhibited remarkable catalytic performance towards soot oxidation with a T50 of 290.5 â„ƒ under 10 % O2/N2. Catalyst characterization investigated by Scanning Electron Microscope (SEM), quasi in-situ X-ray Photoelectron Spectroscopy (XPS), in-situ Raman, etc. revealed that this outstanding promotion in catalytic activity can be principally ascribed to the formation of the CeO2/Co3O4 interface. An appropriate CeO2 dosage maximized the contact and interaction between Co3O4 and CeO2, resulting in the largest CeO2/Co3O4 interface featured with abundant generated superoxide species and activated surface lattice oxygen. Density functional theory (DFT) calculations were also carried out for the oxygen vacancy formation energy, Gibbs free energy, etc. In presence of the CeO2/Co3O4 interface, a charge density redistribution around the adsorbed reactants at oxygen vacancies could be formed, owing to the efficient charge transfer enhanced by the electron-appealing effect. The change in electronic structure favored reducing the oxygen vacancy formation energy and boosting the lattice oxygen activation induced by the hybridized Co-O-Ce bonds, finally lowering the adsorption and activation barriers for reactive species and accelerating the reaction kinetics.

Cold-Start NOx Mitigation by Passive Adsorption Using Pd-Exchanged Zeolites: From Material Design to Mechanism Understanding and System Integration.

It remains a major challenge to abate efficiently the harmful nitrogen oxides (NOx) in low-temperature diesel exhausts emitted during the cold-start period of engine operation. Passive NOx adsorbers (PNA), which could temporarily capture NOx at low temperatures (below 200 °C) and release the stored NOx at higher temperatures (normally 250-450 °C) to downstream selective catalytic reduction unit for complete abatement, hold promise to mitigate cold-start NOx emissions. In this review, recent advances in material design, mechanism understanding, and system integration are summarized for PNA based on palladium-exchanged zeolites. First, we discuss the choices of parent zeolite, Pd precursor, and synthetic method for the synthesis of Pd-zeolites with atomic Pd dispersions, and review the effect of hydrothermal aging on the properties and PNA performance of Pd-zeolites. Then, we show how different experimental and theoretical methodologies can be integrated to gain mechanistic insights into the nature of Pd active sites, the NOx storage/release chemistry, as well as the interactions between Pd and typical components/poisons in engine exhausts. This review also gathers several novel designs of PNA integration into modern exhaust after-treatment systems for practical application. At the end, we discuss the major challenges, as well as important implications, for the further development and real application of Pd-zeolite-based PNA in cold-start NOx mitigation.

The novel chitosan-amphoteric starch dual flocculants for enhanced removal of Microcystis aeruginosa and algal organic matter.

A novel flocculation strategy for simultaneously removing Microcystis aeruginosa and algal organic matter (AOM) was proposed using chitosan-amphoteric starch (C-A) dual flocculants in an efficient, cost-effective and ecologically friendly way, providing new insights for harmful algal blooms (HABs) control. A dual-functional starch-based flocculant, amphoteric starch (AS) with high anion degree of substitution (DSA) and cation degree of substitution (DSC), was prepared using a cationic moiety of 3-chloro-2-hydroxypropyltrimethylammonium chloride (CTA) coupled with an anion moiety of chloroacetic acid onto the backbone of starch simultaneously. In combination of the results of FTIR, XPS, 1H NMR, 13C NMR, GPC, EA, TGA and SEM, it was evidenced that the successfully synthesized AS with excellent structural characteristics contributed to the enhanced flocculation of M. aeruginosa. Furthermore, the novel C-A dual flocculants could achieve not only the removal of >99.3 % of M. aeruginosa, but also the efficacious flocculation of algal organic matter (AOM) at optimal concentration of (0.8:24) mg/L, within a wide pH range of 3-11. The analysis of zeta potential and cellular morphology revealed that the dual effects of both enhanced charge neutralization and notable netting-bridging played a vital role in efficient M. aeruginosa removal.

Economical and Sustainable Synthesis of Small-Pore Chabazite Catalysts for NOx Abatement by Recycling Organic Structure-Directing Agents.

The application of small-pore chabazite-type SSZ-13 zeolites, key materials for the reduction of nitrogen oxides (NOx) in automotive exhausts and the selective conversion of methane, is limited by the use of expensive N,N,N-trimethyl-1-ammonium adamantine hydroxide (TMAdaOH) as an organic structure-directing agent (OSDA) during hydrothermal synthesis. Here, we report an economical and sustainable route for SSZ-13 synthesis by recycling and reusing the OSDA-containing waste liquids. The TMAdaOH concentration in waste liquids, determined by a bromocresol green colorimetric method, was found to be a key factor for SSZ-13 crystallization. The SSZ-13 zeolite synthesized under optimized conditions demonstrates similar physicochemical properties (surface area, porosity, crystallinity, Si/Al ratio, etc.) as that of the conventional synthetic approach. We then used the waste liquid-derived SSZ-13 as the parent zeolite to synthesize Cu ion-exchanged SSZ-13 (i.e., Cu-SSZ-13) for ammonia-mediated selective catalytic reduction of NOx (NH3-SCR) and observed a higher activity as well as better hydrothermal stability than Cu-SSZ-13 by conventional synthesis. In situ infrared and ultraviolet-visible spectroscopy investigations revealed that the superior NH3-SCR performance of waste liquid-derived Cu-SSZ-13 results from a higher density of Cu2+ sites coordinated to paired Al centers on the zeolite framework. The technoeconomic analysis highlights that recycling OSDA-containing waste liquids could reduce the raw material cost of SSZ-13 synthesis by 49.4% (mainly because of the higher utilization efficiency of TMAdaOH) and, meanwhile, the discharging of wastewater by 45.7%.