Study of spatial and temporal aging characteristic of catalyzed diesel particulate filter catalytic performance used for diesel vehicle

AbstractCatalyzed diesel particulate filters (CDPFs) have been widespread used as a technically and economically feasible mean for meeting increasingly stringent emissions limits. An important issue affecting the performance of a CDPF is its aging with using time. In this paper, the effects of noble metal loadings, regions and using mileage on the aging performance of a CDPF were investigated by methods of X-ray diffraction (XRD), X-ray photoelectron spectroscopy and catalytic activity evaluation. Results showed that aging of the CDPF shifted the XRD characteristic diffraction peaks towards larger angles and increased the crystallinity, showing a slowing downward trend with the increase of the noble metal loadings. In addition, the increase of the noble metal loading would slow down the decline of Pt and Pt4+ concentration caused by aging. The characteristic temperatures of CO, C3H8 conversion and NO2 production increased after aging, and the more the noble metal loadings, the higher the range of the increase. But noticeably, excessive amounts of noble metals would not present the corresponding anti-aging properties. Specifically, the degree of aging in the inlet region was the deepest, the following is the outlet region, and the middle region was the smallest, which were also reflected in the increase range of crystallinity, characteristic temperatures of CO, C3H8 conversion and NO2 production, as well as the decrease range of Pt and Pt4+ concentrations. The increase of aging mileage reduced the size of the aggregates of the soot and ash in CDPFs, however, improved the degree of tightness between particles. Meanwhile Carbon (C) concentration in the soot and ash increased with the aging mileage.

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Influence of Semiconductor Morphology on Photocatalytic Activity of Plasmonic Photocatalysts: Titanate Nanowires and Octahedral Anatase Nanoparticles

Nanomaterials ◽

10.3390/nano9101447 ◽

2019 ◽

Vol 9 (10) ◽

pp. 1447 ◽

Cited By ~ 3

Author(s):

Wei ◽

Endo-Kimura ◽

Wang ◽

Colbeau-Justin ◽

Kowalska

Keyword(s):

Acetic Acid ◽

Photocatalytic Activity ◽

Noble Metal ◽

Photoelectron Spectroscopy ◽

Noble Metals ◽

Diffuse Reflectance Spectroscopy ◽

Localized Surface Plasmon ◽

Time Resolved ◽

X Ray ◽

Titanate Nanowires

Octahedral anatase particles (OAP) with eight exposed and thermodynamically most stable (101) facets were prepared by an ultrasonication-hydrothermal (US-HT) reaction from potassium titanate nanowires (TNW). The precursor (TNW) and the product (OAP) of US-HT reaction were modified with nanoparticles of noble metals (Au, Ag or Pt) by photodeposition. Samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), diffuse reflectance spectroscopy (DRS), scanning transmission electron microscopy (STEM) and time-resolved microwave conductivity (TRMC). The photocatalytic activity was investigated in three reaction systems, i.e., anaerobic dehydrogenation of methanol and oxidative decomposition of acetic acid under UV/vis irradiation, and oxidation of 2-propanol under vis irradiation. It was found that hydrogen liberation correlated with work function of metals, and thus the most active were platinum-modified samples. Photocatalytic activities of bare and modified OAP samples were much higher than those of TNW samples, probably due to anatase presence, higher crystallinity and electron mobility in faceted NPs. Interestingly, noble metals showed different influence on the activity depending on the semiconductor support, i.e., gold-modified TNW and platinum-modified OAP exhibited the highest activity for acetic acid decomposition, whereas silver- and gold-modified samples were the most active under vis irradiation, respectively. It is proposed that the form of noble metal (metallic vs. oxidized) as well as the morphology (well-organized vs. uncontrolled) have a critical effect on the overall photocatalytic performance. TRMC analysis confirmed that fast electron transfer to noble metal is a key factor for UV activity. It is proposed that the efficiency of plasmonic photocatalysis (under vis irradiation) depends on the oxidation form of metal (zero-valent preferable), photoabsorption properties (broad localized surface plasmon resonance (LSPR)), kind of metal (silver) and counteraction of “hot” electrons back transfer to noble metal NPs (by controlled morphology and high crystallinity).

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Biodiesel Production on Monometallic Pt, Pd, Ru, and Ag Catalysts Supported on Natural Zeolite

Materials ◽

10.3390/ma14010048 ◽

2020 ◽

Vol 14 (1) ◽

pp. 48

Author(s):

Pawel Mierczynski ◽

Magdalena Mosińska ◽

Lukasz Szkudlarek ◽

Karolina Chalupka ◽

Misa Tatsuzawa ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Natural Zeolite ◽

Noble Metals ◽

Methyl Esters ◽

Physicochemical Characteristics ◽

Biodiesel Production ◽

X Ray Diffraction ◽

X Ray ◽

Yield Values ◽

Temperature Programmed

Biodiesel production from rapeseed oil and methanol via transesterification reaction facilitated by various monometallic catalyst supported on natural zeolite (NZ) was investigated. The physicochemical characteristics of the synthesized catalysts were studied by X-ray diffraction (XRD), Brunauer–Emmett–Teller method (BET), temperature-programmed-reduction in hydrogen (H2-TPR), temperature-programmed-desorption of ammonia (NH3-TPD), Scanning Electron Microscope equipped with EDX detector (SEM-EDS), and X-ray photoelectron spectroscopy (XPS) methods. The highest activity and methyl ester yields were obtained for the Pt/NZ catalyst. This catalyst showed the highest triglycerides conversion of 98.9% and fatty acids methyl esters yields of 94.6%. The activity results also confirmed the high activity of the carrier material (NZ) itself in the investigated reaction. Support material exhibited 90.5% of TG conversion and the Fatty Acid Methyl Esters yield (FAME) of 67.2%. Introduction of noble metals improves the TG conversion and FAME yield values. Increasing of the metal loading from 0.5 to 2 wt.% improves the reactivity properties of the investigated catalysts.

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Preparation of Novel Ag–Si–TiO2 Composite and Research on Its Photocatalytic Degradation of Formaldehyde

Science of Advanced Materials ◽

10.1166/sam.2021.3864 ◽

2021 ◽

Vol 13 (3) ◽

pp. 371-380

Author(s):

Yongjun Wu ◽

Nina Xie ◽

Lu Yu

Keyword(s):

Photoelectron Spectroscopy ◽

Removal Rate ◽

Sol Gel ◽

Catalytic Performance ◽

Formaldehyde Concentration ◽

Order Kinetic ◽

Solution Ph ◽

Visible Absorption ◽

X Ray ◽

Co Doped

A novel Ag–Si–TiO2 composite was prepared via sol–gel method for removing residual formaldehyde in shiitake mushroom. The structure of Ag–Si–TiO2 composite was characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses. Ultraviolet-visible absorption spectroscopy (UV-Vis) and N2 adsorption-desorption tests showed that Ag and Si co-doped decreased the band gap, the Brunauer-Emmett-Teller (BET) specific surface area of the samples increased and the recombination probability of electron-hole pairs (e--h+) reduced. Effect on removal rate of formaldehyde with different Ag-Si co-doped content, formaldehyde concentration and solution pH were investigated, and the results showed that 6.0 wt%Ag-3.0 wt%Si-TiO2 samples had an optimum catalytic performance, and the degradation efficiency reached 96.6% after 40 W 365 nm UV lamp irradiation for 360 min. The kinetics of formaldehyde degradation by Ag–Si–TiO2 composite photocatalyst could be described by Langmuir-Hinshelwood first-order kinetic model.

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Influence of Sulfur-Containing Sodium Salt Poisoned V2O5–WO3/TiO2 Catalysts on SO2–SO3 Conversion and NO Removal

Catalysts ◽

10.3390/catal8110541 ◽

2018 ◽

Vol 8 (11) ◽

pp. 541 ◽

Cited By ~ 3

Author(s):

Haiping Xiao ◽

Chaozong Dou ◽

Hao Shi ◽

Jinlin Ge ◽

Li Cai

Keyword(s):

Photoelectron Spectroscopy ◽

No Reduction ◽

Catalytic Performance ◽

Acid Sites ◽

Impregnation Method ◽

So2 Oxidation ◽

Sodium Salts ◽

X Ray ◽

Temperature Programmed ◽

Physical Features

A series of poisoned catalysts with various forms and contents of sodium salts (Na2SO4 and Na2S2O7) were prepared using the wet impregnation method. The influence of sodium salts poisoned catalysts on SO2 oxidation and NO reduction was investigated. The chemical and physical features of the catalysts were characterized via NH3-temperature programmed desorption (NH3-TPD), H2-temperature programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), and Fourier Transform Infrared Spectroscopy (FT-IR). The results showed that sodium salts poisoned catalysts led to a decrease in the denitration efficiency. The 3.6% Na2SO4 poisoned catalyst was the most severely deactivated with denitration efficiency of only 50.97% at 350 °C. The introduction of SO42− and S2O72− created new Brønsted acid sites, which facilitated the adsorption of NH3 and NO reduction. The sodium salts poisoned catalysts significantly increased the conversion of SO2–SO3. 3.6%Na2S2O7 poisoned catalyst had the strongest effect on SO2 oxidation and the catalyst achieved a maximum SO2–SO3-conversion of 1.44% at 410 °C. Characterization results showed sodium salts poisoned catalysts consumed the active ingredient and lowered the V4+/V5+ ratio, which suppressed catalytic performance. However, they increased the content of chemically adsorbed oxygen and the strength of V5+=O bonds, which promoted SO2 oxidation.

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Rhodium Oxide Surface-Loaded Gas Sensors

Nanomaterials ◽

10.3390/nano8110892 ◽

2018 ◽

Vol 8 (11) ◽

pp. 892 ◽

Cited By ~ 12

Author(s):

Anna Staerz ◽

Inci Boehme ◽

David Degler ◽

Mounib Bahri ◽

Dmitry Doronkin ◽

...

Keyword(s):

Metal Oxide ◽

Noble Metal ◽

Noble Metals ◽

Metal Cluster ◽

Empirical Work ◽

Oxide Surface ◽

Metallic State ◽

X Ray ◽

Rhodium Clusters ◽

Sensing Characteristics

In order to increase their stability and tune-sensing characteristics, metal oxides are often surface-loaded with noble metals. Although a great deal of empirical work shows that surface-loading with noble metals drastically changes sensing characteristics, little information exists on the mechanism. Here, a systematic study of sensors based on rhodium-loaded WO3, SnO2, and In2O3—examined using X-ray diffraction, high-resolution scanning transmission electron microscopy, direct current (DC) resistance measurements, operando diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, and operando X-ray absorption spectroscopy—is presented. Under normal sensing conditions, the rhodium clusters were oxidized. Significant evidence is provided that, in this case, the sensing is dominated by a Fermi-level pinning mechanism, i.e., the reaction with the target gas takes place on the noble-metal cluster, changing its oxidation state. As a result, the heterojunction between the oxidized rhodium clusters and the base metal oxide was altered and a change in the resistance was detected. Through measurements done in low-oxygen background, it was possible to induce a mechanism switch by reducing the clusters to their metallic state. At this point, there was a significant drop in the overall resistance, and the reaction between the target gas and the base material was again visible. For decades, noble metal loading was used to change the characteristics of metal-oxide-based sensors. The study presented here is an attempt to clarify the mechanism responsible for the change. Generalities are shown between the sensing mechanisms of different supporting materials loaded with rhodium, and sample-specific aspects that must be considered are identified.

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Synthesis of Novel g-C3N4/NH2-MIL-88B(Fe) Composite Photocatalysis for Efficient Ciprofloxacin Degradation Under Simulated Sunlight Irradiation

NANO ◽

10.1142/s1793292021500636 ◽

2021 ◽

pp. 2150063

Author(s):

Jungang Yi ◽

Kun Wu ◽

Huadong Wu ◽

Jia Guo ◽

Linfeng Zhang ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Adsorption Property ◽

Catalytic Performance ◽

Step Method ◽

Area Formula ◽

Aquatic Life ◽

X Ray ◽

Transmission Electron ◽

Uniform Dispersion ◽

Composite Photocatalysts

The presence of the antibiotics in the wastewater has posed a huge risk to aquatic life and human health. It is a great significance to develop an effective technology to treat the antibiotics-containing wastewater. In this study, a series of g-C3N4/NH2-MIL-88B(Fe) composite photocatalysts are synthesized through a simple one-step method. The structure and optical properties of prepared photocatalysts are detected by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV–Vis absorption spectra (UV–Vis DRS), photoluminescence (PL) spectroscopy and transient photocurrent techniques, respectively. FESEM and TEM show that MOF is uniformly dispersed in petaloid g-C3N4. The uniform dispersion of Fe-MOFs in the heterojunction composites increases the specific surface area ([Formula: see text] of g-C3N4, which results in a great adsorption property for the nanocomposite. The capture experiment shows that [Formula: see text]O[Formula: see text] and h[Formula: see text] are the main active substances in ciprofloxacin (CIP) degradation. These prepared composite photocatalysts exhibit excellent CIP photodegradation activity under visibly light irradiation with an apparent rate constant of 0.0127[Formula: see text]min[Formula: see text] (3.74 times as the rate of single component). The remarkable catalytic performance can be ascribed to the fact that the g-C3N4/NH2-MIL-88B(Fe) heterojunction inhibits the recombination of photoinduced electron–hole pairs and improved the visible light absorption.

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Synthesis of Hollow Flower-Like Fe3O4/MnO2/Mn3O4 Magnetically Separable Microspheres with Valence Heterostructure for Dye Degradation

Catalysts ◽

10.3390/catal9070589 ◽

2019 ◽

Vol 9 (7) ◽

pp. 589 ◽

Cited By ~ 4

Author(s):

Mingliang Ma ◽

Yuying Yang ◽

Yan Chen ◽

Fei Wu ◽

Wenting Li ◽

...

Keyword(s):

Electron Microscopy ◽

Visible Light ◽

Photoelectron Spectroscopy ◽

Organic Contaminants ◽

Dye Degradation ◽

Catalytic Performance ◽

X Ray ◽

Composite Microspheres ◽

Magnetically Separable ◽

Mno2 Nanosheet

In this manuscript, hollow flower-like ferric oxide/manganese dioxide/trimanganese tetraoxide (Fe3O4/MnO2/Mn3O4) magnetically separable microspheres were prepared by combining a simple hydrothermal method and reduction method. As the MnO2 nanoflower working as precursor was partially reduced, Mn3O4 nanoparticles were in situ grown from the MnO2 nanosheet. The composite microspheres were characterized in detail by employing scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), vibration sample magnetometer (VSM) and UV–visible spectrophotometer (UV–vis). Under visible light conditions, the test for degrading rhodamine B (RhB) was used to verify the photocatalytic activity of the photocatalyst. The results showed that the efficiency of the Fe3O4/MnO2/Mn3O4 photocatalyst in visible light for 130 min is 94.5%. The catalytic activity of photocatalyst far exceeded that of the Fe3O4/MnO2 component, and after four cycles, the catalytic performance of the catalyst remained at 78.4%. The superior properties of the photocatalyst came from improved surface area, enhanced light absorption, and efficient charge separation of the MnO2/Mn3O4 heterostructure. This study constructed a green and efficient valence heterostructure composite that created a promising photocatalyst for degrading organic contaminants in aqueous environments.

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Capping Agent Effect on Pd-Supported Nanoparticles in the Hydrogenation of Furfural

Catalysts ◽

10.3390/catal10010011 ◽

2019 ◽

Vol 10 (1) ◽

pp. 11 ◽

Cited By ~ 3

Author(s):

Shahram Alijani ◽

Sofia Capelli ◽

Stefano Cattaneo ◽

Marco Schiavoni ◽

Claudio Evangelisti ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Active Sites ◽

Catalytic Performance ◽

Shielding Effect ◽

Capping Agents ◽

X Ray ◽

Supported Nanoparticles ◽

Liquid Phase Hydrogenation ◽

Diallyldimethylammonium Chloride ◽

Transmission Electron

The catalytic performance of a series of 1 wt % Pd/C catalysts prepared by the sol-immobilization method has been studied in the liquid-phase hydrogenation of furfural. The temperature range studied was 25–75 °C, keeping the H2 pressure constant at 5 bar. The effect of the catalyst preparation using different capping agents containing oxygen or nitrogen groups was assessed. Polyvinyl alcohol (PVA), polyvinylpyrrolidone (PVP), and poly (diallyldimethylammonium chloride) (PDDA) were chosen. The catalysts were characterized by ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The characterization data suggest that the different capping agents affected the initial activity of the catalysts by adjusting the available Pd surface sites, without producing a significant change in the Pd particle size. The different activity of the three catalysts followed the trend: PdPVA/C > PdPDDA/C > PdPVP/C. In terms of selectivity to furfuryl alcohol, the opposite trend has been observed: PdPVP/C > PdPDDA/C > PdPVA/C. The different reactivity has been ascribed to the different shielding effect of the three ligands used; they influence the adsorption of the reactant on Pd active sites.

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Preparation of pod-shaped TiO 2 and Ag@TiO 2 nano burst tubes and their photocatalytic activity

Royal Society Open Science ◽

10.1098/rsos.191019 ◽

2019 ◽

Vol 6 (9) ◽

pp. 191019 ◽

Cited By ~ 2

Author(s):

Shang Wang ◽

Zhaolian Han ◽

Tingting Di ◽

Rui Li ◽

Siyuan Liu ◽

...

Keyword(s):

Electron Microscopy ◽

Photocatalytic Activity ◽

Oxalic Acid ◽

Ultraviolet Light ◽

Photoelectron Spectroscopy ◽

Degradation Process ◽

Catalytic Performance ◽

Tetrabutyl Titanate ◽

Order Kinetic ◽

X Ray

The pod-shaped TiO 2 nano burst tubes (TiO 2 NBTs) were prepared by the combination of electrospinning and impregnation calcination with oxalic acid (H 2 C 2 O 4 ), polystyrene (PS) and tetrabutyl titanate. The silver nanoparticles (AgNPs) were loaded onto the surface of TiO 2 NBTs by ultraviolet light reduction method to prepare pod-shaped Ag@TiO 2 NBTs. In this work, we analysed the effect of the amount of oxalic acid on the cracking degree of TiO 2 NBTs; the effect of the concentration of AgNO 3 solution on the particle size and loading of AgNPs on the surface of TiO 2 NBTs. Scanning electron microscopy and transmission electron microscopy investigated the surface morphology of samples. X-ray diffraction and X-ray photoelectron spectroscopy characterized the structure and composition of samples. Rhodamine B (RhB) solution was used to evaluate the photocatalytic activity of pod-shaped TiO 2 NBTs and Ag@TiO 2 NBTs. The results showed that TiO 2 NBTs degraded 91.0% of RhB under ultraviolet light, Ag@TiO 2 NBTs degraded 95.5% under visible light for 75 and 60 min, respectively. The degradation process of both samples was consistent with the Langmuir–Hinshelwood first-order kinetic equation. Therefore, the catalytic performance of the sample is: Ag@TiO 2 NBTs > TiO 2 NBTs > TiO 2 nanotubes.

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Preparation and Photocatalytic Performances of WO3/TiO2 Composite Nanofibers

Journal of Chemistry ◽

10.1155/2020/2390486 ◽

2020 ◽

Vol 2020 ◽

pp. 1-12

Author(s):

Xiuping Han ◽

Binghua Yao ◽

Keying Li ◽

Wenjing Zhu ◽

Xuyuan Zhang

Keyword(s):

Photoelectron Spectroscopy ◽

Photocatalytic Oxidation ◽

Composite Nanofibers ◽

Photogenerated Electron ◽

Xrd Analysis ◽

Catalytic Performance ◽

Active Species ◽

X Ray ◽

Bet Analysis ◽

Electron Holes

The use of sunlight for photocatalytic oxidation is an ideal strategy, but it is limited by factors such as insufficient light absorption intensity of the photocatalyst and easy recombination of photogenerated electron holes. TiO2 is favored by researchers as an environment-friendly catalyst. In this paper, TiO2 is combined with WO3 to obtain a nanofiber with excellent catalytic performance under sunlight. The WO3/TiO2 composite nanofibers were synthesized by using the electrospinning method. The X-ray diffraction (XRD) analysis indicated that WO3 was successfully integrated onto the surface of TiO2. The photodegradation performance and photocurrent analysis of the prepared nanofibers showed that the addition of WO3 really improved the photocatalytic performance of TiO2 nanofibers, methylene blue (MB) degradation rate increased from 72% to 96%, and 5% was the optimal composite mole percentage of W to Ti. The scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectra (UV-Vis DRS), and Brunauer-Emmett-Teller (BET) analysis further characterized the properties of 5% WO3/TiO2 nanofibers. The H2 generation rate of 5% WO3/TiO2 nanofibers was 107.15 μmol·g−1·h−1, in comparison with that of TiO2 nanofibers (73.21 μmol·g−1·h−1) under the same condition. The 5% WO3/TiO2 produced ·OH under illumination, which played an important role in the MB degradation. Also, the enhanced photocatalytic mechanism was also proposed based on the detailed analysis of the band gap and the active species trapping experiment. The results indicated that the effective separation of Z-scheme photogenerated electron-hole pairs and transfer system constructed between TiO2 and WO3 endowed the excellent photocatalytic activity of 5% WO3/TiO2 nanofibers.

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