We employed a polymer network to understand what properties of pyrogenic carbonaceous matter (PCM; ., activated carbon) confer its reactivity, which we hereinafter referred to as PCM-like polymers (PLP). This approach allows us to delineate the role of functional groups and micropore characteristics using 2,4,6-trinitrotoluene (TNT) as a model contaminant. Six PLP were synthesized via cross-coupling chemistry with specific functionality (-OH, -NH, -N(CH), or ) and pore characteristics (mesopore, micropore). Results suggest that PCM functionality catalyzed the reaction by: (1) serving as a weak base (-OH, -NH) to attack TNT, or (2) accumulating OH near PCM surfaces (). Additionally, TNT hydrolysis rates, pH and co-ion effects, and products were monitored. Microporous PLP accelerated TNT decay compared to its mesoporous counterpart, as further supported by molecular dynamics modeling results. We also demonstrated that quaternary ammonium-modified activated carbon enhanced TNT hydrolysis. These findings have broad implications for pollutant abatement and catalyst design.

Ribavirin (RBV) is an antiviral drug used for treating COVID-19 infection. Its release into natural waters would threaten the health of aquatic ecosystem. This study reports an effective approach to degrade RBV by the trace N-oxyl compounds (2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) and N-Hydroxyphthalimide (NHPI)) enhanced UV activated free chlorine (UV/Chlorine) process. The results indicated that TEMPO and NHPI at low concentrations (0.1 μM and 1 μM, respectively) could strongly enhance RBV degradation in both deionized water with different pHs and practical surface water. The enhancement was verified to be attributed to the transformation of TEMPO and NHPI into their reactive forms (i.e., TEMPO and PINO), which generations deeply relied on radicals. The two N-oxyl compounds inhibit ClO• yield by hindering the reaction of free chlorine vs. HO• and Cl•. The analyses on acute toxicities of RBV degradation products indicate that UV/Chlorine/N-oxyl compounds process can detoxify RBV more efficiently than UV/Chlorine process.

The current study investigates a novel redox technology based on synthetic franklinite-like zinc-ferrite nanomaterial with magnetic properties and redox nature for potential use in water treatment. Physicochemical characterization revealed the nanoscale size and ABO spinel configuration of the zinc-ferrite nanomaterial. The redox activity of nanoparticles was tested for degradation of diclofenac (DCF) pharmaceutical in water, without any added external oxidants and under dark experimental conditions. Results revealed ~90% degradation in DCF (10 μM) within 2 min of reaction using 0.17 g/L ZnFeO. Degradation of DCF was due to chemical reduction by surface electrons on zinc-ferrite and oxidation by oxygen-based radicals. Three byproducts from reduction route and eight from oxidation pathways were identified in the reaction system. Reaction pathways were suggested based on the identified byproducts. Results demonstrated the magnetic zinc-ferrite is a standalone technology that has a great promise for rapid degradation of organic contaminants, such as DCF in water.

The approach of this timely review considers the current literature that is focused on the interface nanostructure/cell-wall microorganism to understand the annihilation mechanism. Morphological studies use optical and electronic microscopes to determine the physical damage on the cell-wall and the possible cell lysis that confirms the viability and microorganism death. The key parameters of the tailoring the surface of the photoactive nanostructures such as the metal functionalization with bacteriostatic properties, hydrophilicity, textural porosity, morphology and the formation of heterojunction systems, can achieve the effective eradication of the microorganisms under natural conditions, ranging from practical to applications in environment, agriculture, and so on. However, to our knowledge, a comprehensive review of the microorganism/nanomaterial interface approach has rarely been conducted. The final remarks point the ideal photocatalytic way for the effective prevention/eradication of microorganisms, considering the resistance that the microorganism could develop without the appropriate regulatory aspects for human and ecosystem safety.

Carbon dots (CDs) were synthesized by a microwave-mediated method and separated by size exclusion chromatography into three different size fractions. There was no correlation of the size with photoluminescence (PL) emission wavelength, which shows that the PL mechanism is not quantum-size dependent. UV/vis absorption and diffuse reflectance spectroscopies showed that the light absorption properties as well as the band gap of the CDs changed with the size of the particle. The combination of FTIR and XPS measurements revealed the composition on the surface of each fraction. The three CDs fractions were separately used in the photocatalytic degradation of organic dyes under simulated sunlight irradiation. The catalytic activity of the as-prepared CDs was found to increase as the size of the particles decreased. Complete degradation of both rhodamine B (RhB) and methylene blue (MB) was achieved in 150 min by the 2-nm CDs. The scavenger studies showed that the holes and superoxide radicals are the main species involved in the photocatalytic degradation of the dye by the 2-nm CDs. These CDs displayed high stability in the degradation of organic dyes for multiple cycles. The 2-nm CDs displayed promising photocatalytic degradation of p-nitrophenol (PNP) . These results demonstrate for the first time the application of bare carbon dots in the degradation of environmental contaminants.

In the present study, the synthesis of an organic group-modified alumina by the sol-gel method is proposed. This material has shown to have an enhanced catalytic performance with grafted organic groups and showed an improved stability. The prepared material has shown to have several groups and an enhanced surface acidity. The alumina acidity was improved by incorporating thiol groups by grafting method, which promotes the tautomerization of fructose to its furanose form. Furthermore, the grafting of sulfonic groups catalyzes its dehydration. The modified alumina was thermally treated up to 200 °C to improve the functional groups stability. After, this modified material was packed into a continuous reactor system, designed and built by this group, to obtain 5-hydroxymethylfurfural (5-HMF) from fructose dissolved in a single-phase solution of tetrahydrofuran (THF) and HO (4:1 w/w). The catalytic activity of this material was evaluated by the reaction of fructose dehydration at different reaction temperatures (60, 70, 80 and 90 °C). Fructose conversion and selectivity toward 5-HMF were determined by high performance liquid chromatography (HPLC), obtaining 95% and 73% respectively for the highest temperature. The catalyst showed an efficient stability after 24 hours in continuous flow at 70 °C. The loss of sulfur content was 15%, but the fructose conversion yield and the selectivity to 5-HMF after 24 hours of continuous reaction did not undergo significant changes (less than 5%). The nuclear magnetic resonance (NMR) tests confirmed the presence of the thiol and sulfonic groups before and after 24 hours of reaction, as well as the conservation of the same structure, demonstrating the efficient catalytic performance of the material. The catalysts were characterized by nitrogen adsorption/desorption, X-ray diffraction and infrared (IR) spectroscopy. Also, before and after use by utilizing elemental analysis and cross-polarization magic-angle spinning (CPMAS) and dynamic-nuclear polarization (DNP)-enhanced and CPMAS as well as directly excited magic-angle spinning (MAS) NMR methods in solid-state.

In this work, it is proposed an environmental friendly sonophotocatalytic approach to efficiently treat polluted waters from industrial dyes exploiting ZnO micro- and nano-materials. For the first time, we deeply investigated the generation of reactive oxygen species (ROS) under ultrasound stimulation of different ZnO structures by Electron Paramagnetic Resonance Spectroscopy (EPR). Indeed, five zinc oxide (ZnO) micro- and nano-structures, Desert Roses (DRs), Multipods (MPs), Microwires (MWs), Nanoparticles (NPs) and Nanowires (NWs), were studied for the Rhodamine B (RhB) sonodegradation under ultrasonic irradiation. The DRs microparticles demonstrated the best sonocatalytic performance (100% degradation of RhB in 180 min) and the highest OH radicals generation under ultrasonic irradiation. Strikingly, the coupling of ultrasound and sun-light irradiation in a sonophotodegradation approach led to 100% degradation efficiency, color reduction, of RhB in just 10 min, revealing a great positive synergy between the photocatalytic and sonocatalytic mechanisms. The RhB sonophotocatalytic degradation was also evaluated at different initial dye concentrations and with the presence of anions in solution. It was demonstrated a good stability over repeated cycles of dye treatment, which probe the applicability of this technique with industrial effluents. In conclusion, sonophotocatalytic degradation synergizing sunlight and ultrasound in the presence of DRs microparticles shows a great potential and a starting point to investigate further the efficient treatment of organic dyes in wastewater.

Synthesis of high-performance and cost-effective electrocatalysts towards hydrazine electrooxidation is vital to develop the direct hydrazine fuel cell (DHFC) as a viable energy conversion technology. Herein, we report a combined experimental and theoretical study of nickel phosphides (NiP) as promising catalysts for hydrazine electrooxidation. NiP nanowire array supported on a Ni foam (NF) was synthesized by a one-step phosphorization method using hypophosphite as a P-source. NiP and NiP phases are observed as the products of the direct phosphorization of commercial NF under the applied conditions with NiP nanoparticles exclusively distributing on the surface of NiP. The NiP/NF catalyst exhibits a synergetic capabilities of exceptionally high activity, excellent durability and nearly 100% selectivity towards the complete electrooxidation of hydrazine in alkaline condition, which is among the best performance reported on hydrazine electrooxidation catalysts. First-principles calculations have been conducted to gain insight into the catalytic mechanism of Ni phosphides towards hydrazine electrooxidation.

Octahedral anatase particles (OAP, with eight equivalent {101} facets) and decahedral anatase particles (DAP, with two additional {001} facets) were modified with nanoparticles of noble metals (Au, Ag, Cu). The titania morphology, expressed by the presence of different arrangements of exposed crystal facets, played a key role in the photocatalytic properties of metal-modified faceted titania. In the UV/vis systems, two-faceted configuration of DAP was more favorable for the reaction efficiency than single-faceted OAP because of an efficient charge separation described by the transfer of electrons to {101} facets and holes to {001} facets. Time-resolved microwave conductivity (TRMC) and reversed double-beam photoacoustic spectroscopy (RDB-PAS) confirmed that distribution of electron traps (ET) and mobility of electrons were key-factors of photocatalytic activity. In contrast, metal-modified OAP samples had higher photocatalytic activity than metal-modified DAP and metal-modified commercial titania samples under visible light irradiation. This indicates that the presence of single type of facets ({101}) is favorable for efficient electron transfer via shallow ET, whereas intrinsic properties of DAP result in fast charge carriers' recombination when gold is deposited on {101} facets (migration of "hot" electrons: Au→{101}→Au).

Reduced graphene oxide hybridized with zero-valent silver and magnetite nanoparticles (NPs) (rGO-Ag/FeO nanohybrids) prepared via nucleation and crystallization was used to activate peroxydisulfate (PDS) for degradation of pharmaceuticals and endocrine disrupting compounds (phenol, acetaminophen, ibuprofen, naproxen, bisphenol A, 17β-estradiol, and 17α-ethinyl estradiol). The deposition of Ag and FeO in rGO nanosheet enhanced the catalytic removal of phenol in the heterogeneous activation of PDS. The adsorption capacities of rGO-Ag/FeO for 10 μM phenol were 1.76, 1.33, and 2.04 μmol g-adsorbent at pH 4, 7, and 10, respectively, which are much higher than those of single NPs studied (Ag, nanoscale zero-valent iron, and rGO). The rGO-Ag/FeO effectively activated PDS to produce strong oxidizing SO·and facilitate an electron transfer on the surface of the nanohybrid. The initial pseudo-first-order rate ( ) constant for phenol degradation in PDS/rGO-Ag/FeO system was 0.46 h at pH 7, which is approximately eight times higher than that in the presence of single NPs ( = 0.04-0.06 h) due to the synergistic effects between adsorption and catalytic oxidation. Among various organic contaminants tested, the simultaneous use of rGO-Ag/FeO (0.1 g/L) and PDS (1 mM) achieved more than 99% degradation of acetaminophen and 17β-estradiol at pH 7. The radical scavenging studies with methanol and natural organic matter indicated that phenol was more likely to be degraded via free SO· and ·OH formation or a non-radical oxidative pathway. Our findings indicate that the rGO-Ag/Fe O nanohybrids can be used as an efficient magnetically-separable nanocatalyst for removal of organic compounds in water and wastewater treatment.

Only limited research has examined the development and application of visible light responsive photocatalytic oxidation (PCO), although such materials have great potential for mitigating concentrations of volatile organic compounds (VOCs) when applied to building surfaces. This study evaluates the performance and characteristics of a visible light responsive photocatalyst, specially, a co-alloyed TiNbON compound with a band energy of 2.3 eV. The PCO material was developed using urea-glass synthesis, characterized by scanning electron microscopy (SEM), diffuse reflectance spectra (DRS), powder X-ray diffraction (PXRD), and Brunauer-Emmett-Teller (BET) methods, and VOC removal efficiency was measured under visible light for toluene (1-5 ppm) at room temperature (21.5°C) and a range of relative humidity (RH: 25 to 65%), flow rate (0.78 to 7.84 cm/s), and irradiance (42 to 95 W/m). A systematic parametric evaluation of kinetic parameters was conducted. In addition, we compared TiNbON with a commercial TiO-based material under black light, estimated TiNbON's long-term durability and stability, and tested its ability to thermally regenerate. Using mass transfer and kinetic analysis, three different Langmuir-Hinshelwood (LH) type reaction rate expressions were proposed and evaluated. A LH model considering one active site and competitive sorption of toluene and water was superior to others. The visible-light driven catalyst was able to remove up to 58 % of the toluene, generated less formaldehyde than the commercial TiO, could be fully regenerated at 150°C, and had reasonable durability and stability. This evaluation of TiNbON shows the potential to remove VOCs and improve air quality for indoor applications. Further research is needed to evaluate the potential for harmful by-products, to identify optimal conditions, and to use field tests to show real-world performance.

Octahedral anatase particles (OAPs), prepared by ultrasonication-hydrothermal reaction (US-HT), were modified with 2 wt% of gold by photodeposition. Conditions of US-HT process such as durations of US and durations of HT were varied to obtain OAPs products different by physicochemical and morphological properties. Au/OAPs samples were characterized by X-ray diffraction (XRD), scanning transmission electron microscopy (STEM), X-ray photoelectron spectroscopy (XPS) and diffuse reflectance spectroscopy (DRS). The photocatalytic activity was tested under UV irradiation for decomposition of acetic acid (CO system) and dehydrogenation of methanol (H system) under aerobic and anaerobic conditions, respectively, and for oxidation of 2-propanol under visible light irradiation. Photodeposition of gold was very fast for all OAPs samples (0.5-10 min) under Ar atmosphere, and the clear correlation between the content of electron traps (ETs) and the induction period, during which nanoparticles (NPs) of gold are formed, indicates that ETs in titania samples are a key-factor for rapidity of gold photodeposition on titania surface. It was found that better morphology of titania (larger content of faceted particles) resulted in formation of larger gold NPs, while small gold NPs were deposited on structural defects. Modification of OAPs with gold NPs resulted in significant enhancement of photocatalytic activity, being e.g., 1.5 (CO system), 7.7 (H system), and even more than 40 under vis irradiation. It was found that both the properties of titania and gold are crucial for resultant photocatalytic activity, but a direct correlation between one structural/physical property and photocatalytic activity could not be obtained since all structural properties changed simultaneously when conditions of photocatalyst preparation (US-HT) were changed. Therefore, gold NPs of controlled sizes were deposited on OAPs product with the best morphology by modified photodeposition method. Clear correlation between photocatalytic activity under visible light and the size of gold NPs indicates that gold properties are decisive for visible light activity rather than titania properties. 3D-FDTD simulations confirm that an increase in the size of gold NPs results in extended surface areas with field enhancement.

Different iron-based cathode catalysts have been studied for oxygen reduction reaction (ORR) in neutral media and then applied into microbial fuel cells (MFC). The catalysts have been synthesized using sacrificial support method (SSM) using eight different organic precursors named Niclosamide, Ricobendazole, Guanosine, Succinylsulfathiazole, Sulfacetamide, Quinine, Sulfadiazine and Pyrazinamide. Linear Sweep Voltammetry (LSV) curves were obtained for the catalysts using a O saturated in 0.1 M potassium phosphate buffer and 0.1 M KCl solution and a Rotating Ring Disk Electrode (RRDE) setup in order to study the ORR characteristics. Additionally, we analyze the peroxide yield obtained for each catalyst which helps us determine the reaction kinetics. Those catalysts have been mixed with activated carbon (AC), carbon black (CB) and PTFE and pressed on a metallic mesh forming a pellet-like gas diffusion electrode (GDE). Results showed that Fe-Ricobendazole, Fe-Niclosamide and Fe-Pyrazinamide had the highest cathode polarization curves and highest power densities output that was above 200 μWcm. Fe-Ricobendazole, Fe-Niclosamide, Fe-Pyrazinamide, Fe-Guanosine Fe-Succinylsulfathiazole and Fe-Sulfacetamide outperformed compared to Pt cathode. Fe-Sulfadiazene and Fe-Quinine performed better than AC used as control but less than Pt. Correlation of surface composition with performance showed that power density achieved is directly related to the total amount of nitrogen, and in particularly, N coordinated to metal and pyridinic and pyrrolic types while larger amounts of graphitic nitrogen result in worse performance.

To eliminate nitrogen oxides (NO), a series of highly ordered mesoporous WO(χ)-CeO nanomaterials (χ represents the mole ratio of W/Ce) were synthesized by using KIT-6 as a hard template, which was used for selective catalytic reduction (SCR) to remove NO with NH at low temperatures. Moreover, the nanomaterials were characterized by TEM, XRD, Raman, XPS, BET, H-TPR, NH-TPD and DRIFTS. It can be found that all of the prepared mesoporous WO(χ)-CeO (χ = 0, 0.5, 0.75, 1 and 1.25) showed highly ordered mesoporous channels. Furthermore, mesoporous WO(1)-CeO exhibited the best removal efficiency of NO, and its NO conversion ratio could reach 100% from 225 ° C to 350 ° C with a gas hourly space velocity of 30 000 h, which was due to higher Ce concentrations, abundant active surface oxygen species and Lewis acid sites based on XPS, H-TPR, NH-TPD and DRIFTS. In addition, several key performance parameters of mesoporous WO(1)-CeO, such as superior water resistance, better alkali metal resistance, higher thermal stability and N selectivity, were systematically studied, indicating that the synthesized mesoporous WO(1)-CeO has great potential for industrial applications.

Herein, we present a novel acid-less synthetic approach for polymerization of aniline synchronized with reduction of graphene oxide to graphene. This method provides uniform deposition of ordered polyaniline nanotubes over the surface of graphene nanosheets. The synthesized graphene-polyaniline nanocomposite has the ability of complete removal of harmful dyes commonly used in industry: such as methyl orange, methylene blue, and rhoadmine B from the waste water under the exposure to natural sunlight. The system can be used as an efficient solar energy operated photocatalyst due to effective suppression of recombination of the charge carriers. The unique spatial structure of the graphene-polyaniline nanocomposite has high chemical stability, can be recycled after photolysis, and allows using in multiple cycles without reduction in its photocatalytic activity. In addition, the graphene-polyaniline nanocomposite exhibits strong near-infrared (NIR) absorption, good photothermal stability, as well as shows substantial thermal energy generation under exposure to 808 or 980 nm NIR lasers. The electrical conductivity of polyaniline nanotubes is improved as a result of their conjugation with graphene nanosheets in the nanocomposite. Owing to its outstanding photocatalytic activity and chemical stability, the reported graphene-polyaniline nanocomposite has a great potential in purification of industrially generated waste water.

The electrode sequence in a mixed flow-through electrochemical cell is evaluated to improve the hydrodechlorination (HDC) of trichloroethylene (TCE) in aqueous solutions. In a mixed (undivided) electrochemical cell, oxygen generated at the anode competes with the transformation of target contaminants at the cathode. In this study, we evaluate the effect of placing the anode downstream from the cathode and using multiple electrodes to promote TCE reduction. Experiments with a cathode followed by an anode (C→A) and an anode followed by a cathode (A→C) were conducted using mixed metal oxide (MMO) and iron as electrode materials. The TCE removal rates when the anode is placed downstream of the cathode (C→A) were 54% by MMO→MMO, 64% by MMO→Fe and 87% by Fe→MMO sequence. Removal rates when the anode is placed upstream of the cathode (A→C) were 38% by MMO→MMO, 58% by Fe→MMO and 69% by MMO→Fe sequence. Placing the anode downstream of the cathode positively improves (by 26%) the degradation of aqueous TCE in a mixed flow-through cell as it minimizes the influence of oxygen generated at the MMO anode on TCE reduction at the cathode. Furthermore, placing the MMO anode downstream of the cathode neutralizes pH and redox potential of the treated solution. Higher flow velocity under the C→A setup increases TCE mass flux reduction rate. Using multiple cathodes and an iron foam cathode up stream of the anode increase the removal rate by 1.6 and 2.4 times, respectively. More than 99% of TCE was removed in the presence of Pd catalyst on carbon and as an iron foam coating. Enhanced reaction rates found in this study imply that a mixed flow-through electrochemical cell with multiple cathodes up stream of an anode is an effective method to promote the reduction of TCE in groundwater.

Palladium catalysts offer the potential for the effective treatment of a variety of priority reducible pollutants in natural waters. In this study, microbially synthesized magnetite nanoparticles were functionalized with Pd(0), creating a highly reactive, magnetically recoverable, nano-scale catalyst (Pd-BnM). This was then investigated for the treatment of model Cr(VI) contaminated solutions at a range of pH values, and also alkaline Cr(VI) contaminated leachates from chromite ore processing residue (COPR); a contaminant issue of global concern. The sample of COPR used in this study was obtained from a site in Glasgow, UK, where extensive Cr(VI) contamination has been reported. In initial experiments Pd-BnM was supplied with H gas or formate as electron donors, and Cr(VI) removal from model synthetic solutions was quantified at various pH values (2-12). Effective removal was noted at neutral to environmentally relevant alkaline (pH 12) pH values, while the use of formate as an electron donor resulted in loss of performance under acidic conditions (pH 2). Reaction kinetics were then assessed with increasing Pd-BnM loading in both model pH 12 Cr(VI) solutions and the COPR leachate. When formate was used as the electron donor for Pd-BnM, to treat COPR leachate, there was significant inhibition of Cr(VI) removal. In contrast, a promotion of reaction rate, was observed when H was employed. Upon sustained reaction with model Cr(VI) solutions, in the presence of excess electron donor (formate or H), appreciable quantities of Cr(VI) were removed before eventual inactivation of the catalyst. Faster onset of inactivation was reported in the COPR leachates, removing 4% and 64% of Cr(VI) observed from model Cr(VI) solutions, when formate and H were used as electron donors, respectively. XAS, TEM-EDX and XPS analysis of the catalysts that had been inactivated in the model solution, showed that the surface had an extensive covering of reduced Cr(III), most likely as a CrOOH phase. COPR reacted catalysts recorded a lower abundance of Cr(III) alongside a high abundance of the leachate components Ca and Si, implicating these elements in the faster onset of inactivation.

A bacterial target-specific titanium oxide (TiO) photocatalyst was developed for the enhancement of selective inactivation of targeted bacteria. An antibacterial composition comprising TiO particles immobilized with a bacterial-specific antibody having affinity to bacteria of interest was prepared via a carbodiimide hydrochloride/N-hydroxysulfosuccinimide (EDC/NHS) coupling reaction between polyacrylic acid (PAA) coated TiO and an antibody. As a model case, an antibody to was conjugated with the PAA-coated TiO (TiO-Ab). We evaluated the enhancement of the antibacterial effect of TiO-Ab against target , compared with its effect on other bacteria that lack affinity for the antibody used. The TiO-Ab inactivated approximately 90% of the at 15 min, whereas the raw TiO inactivated approximately 20% of the after the same period of time under UV irradiation. The TiO-Ab did not show an enhanced antibacterial effect against non-target bacteria. We infer that close contact between TiO particles and , as a result of the specificity of the antibody, can enhance the direct transfer of reactive oxygen species (ROS) generated by TiO particles to the cellular surface under UV irradiation and result in rapid and efficient inactivation of the targeted bacteria. The strategy presented here will facilitate the combination of other receptors and TiO particles for the preparation of highly selective and photocatalytic composites to prevent or remediate contamination by unwanted bacteria in a wide variety of natural and man-made systems.

We investigated the antiviral activity of TiO-coated cordierite foam used in air cleaners, as well as the evaluation methodology. Furthermore, we developed Cu/TiO-coated cordierite foam and investigated the reduction in viral infection ratio. The method for evaluation of antibacterial activity of TiO-coated cordierite foam could also be applied to evaluation of antiviral activity. We showed that Cu/TiO-coated cordierite foam reduced the viral infection ratio to a greater extent than TiO-coated cordierite foam. Our findings suggest that the infection risk by polluted air could be decreased using Cu/TiO-coated cordierite foam in air cleaners.

Under pH 7 - 10 conditions, the mesoporous silica supports proposed for use in water treatment are relatively unstable. In batch experiments conducted in pH 7 solutions, the commonly used support SBA-15 dissolved quickly, releasing approximately 30 mg/L of dissolved silica after 2 hours. In column experiments, more than 45% of an initial mass of 0.25 g SBA-15 dissolved within 2 days when a pH 8.5 solution flowed through the column. In a mixed iron oxide/SBA-15 system, the dissolution of SBA-15 changed the iron oxide reactivity toward H(2)O(2) decomposition, because dissolved silica deposited on iron oxide surface and changed its catalytic active sites. As with SBA-15, other mesoporous silica materials including HMS, MCM-41, four types of functionalized SBA-15, and two types of metal oxide-containing SBA-15 also dissolved under circumneutral pH solutions. The dissolution of mesoporous silica materials raises questions about their use under neutral and alkaline pH in aqueous solutions, because silica dissolution might compromise the behavior of the material.

Mono- and bimetallic Rh and Pt based NO storage-reduction (NSR) catalysts, where the noble metals were deposited on the AlO support or BaCO storage component, have been prepared using a twin flame spray pyrolysis setup. The catalysts were characterized by nitrogen adsorption, CO chemisorption combined with diffuse reflectance infrared Fourier transform spectroscopy, X-ray diffraction, and scanning transmission electron microscopy combined with energy dispersive X-ray spectroscopy. The NSR performance of the catalysts was investigated by fuel lean/rich cycling in the absence and presence of SO (25 ppm) as well as after H desulfation at 750 °C. The performance increased when Rh was located on BaCO enabling good catalyst regeneration during the fuel rich phase. Best performance was observed for bimetallic catalysts where the noble metals were separated, with Pt on AlO and Rh on BaCO. The Rh-containing catalysts generally showed much higher tolerance to SO during fuel rich conditions and lost only little activity during thermal aging at 750 °C.