3D-printed controllable bio-accelerators with sustained release property to boost chromium (VI) inhibited denitrification recovery.

Although soluble bio-accelerators have proven effective in mitigating Cr(VI) inhibition within denitrification system, issues persist in immobilizing bio-accelerators and making them slow-release for sustained regulation. In this study, a novel strategy was proposed to fabricate immobilized bio-accelerators with controlled structure, sustained release property by 3D printing technology. Notably, the sustained release of bio-accelerators from 3D-printed bio-accelerators (3DP-B) lasted for at least 144 h.

Spatial distribution pattern and correlation of dominant species in the arbor layer at a 25 hm forest plot in Lushan Mountain, China.

To explore the spatial pattern of zonal tree species in the subtropical subalpine mountain area on Lushan Mountain, a 25 hm forest plot was established in Yangtianping area of Lushan Mountain following the technical specification of CTFS in 2021. We classified these species into evergreen conifer species, deciduous broad-leaved species and evergreen broad-leaved species based on their leaf shape and deciduous or not to analyze the spatial pattern of dominant species of different types by spatial point pattern method. The results showed that , subsp.

Enhanced etching terminal wastewater treatment and H production by in-situ deposited heavy metals on carbon dots/g-CN photocathode microbial electrolysis cells.

Sustainable and cost-effective semiconducting photocathodes of microbial electrolysis cells (MECs) are attractively promising for efficient treatment of actual industrial wastewaters containing complex recalcitrant organics and multiple heavy metals. Herein carbon dots/graphitic carbon nitride (CDs/g-CN) photocathodes were employed to achieve efficient treatment of actual etching terminal wastewater (ETW) with simultaneous H production in MECs, allowing the effluent meeting national discharge standards (GB39731-2020). The progressively in-situ deposited heavy metals on the CDs/g-CN photocathodes, formed as metal oxides/CDs/g-CN after simple calcinations, further enhanced the ETW treatment (recalcitrant organics mineralization: 42.

The key role of persistent free radicals on the surface of hydrochar and pyrocarbon in the removal of heavy metal-organic combined pollutants.

We show that persistent free radicals (PFRs) on the surface of biochar can produce hydroxyl radicals (•OH) by catalyzing HO to facilitate the removal of the combined pollutant BPA-Cr(VI). Microstructure characterization showed that the structures of pyrocarbon and hydrochar were significantly different when prepared at different temperatures. As the preparation temperature and preparation time for biochar increased, the concentration of PFRs first increased and then decreased.

Regioselective conversions of Hpdta (1,2-propanediaminetetraacetic acid) and Heed3a to their triacetates on peroxotitanates.

1,2-Propanediaminetetraacetic acid (Hpdta = CHON) is degraded selectively to 1-methyl-1,2-propanediaminetriacetic acid (Hpd3a = CHON) with a yield of 75% at room temperature, while N-(2-hydroxyethyl) ethylenediaminetriacetic acid (Heed3a = CHON) is converted with difficulty to ethylenediaminetriacetic acid (Hed3a = CHON) on peroxotitanates(iv), showing the influence of the uncoordinated leaving group. Various species in the reaction sequence are isolated and fully characterized, including (NH)[Ti(O)(Hpdta)]·HO (1), (NH)[Ti(O)(pdta)H(pdta)(O)Ti]·7HO (2), (NH)[Ti(O)(pd3a)]·HO (3) and (NH)[Ti(O)(Heed3a)]·HO (5). Peroxo dimer 2 forms a strong intramolecular hydrogen bond [2.

The feasibility of UF-RO integrated membrane system combined with coagulation/flocculation for hairwork dyeing effluent reclamation.

This paper aims to validate the feasibility of hairwork dyeing effluent (HDE) reclamation using an ultrafiltration (UF)-reverse osmosis (RO) integrated membrane system combined with coagulation-flocculation and sedimentation acquiring the highest possible product water recovery rate along with both satisfactory separation performance and well controlled membrane fouling. Under the circumstance of only physical cleaning involved, the laboratory-scale test yielded a higher and satisfactory reuse ratio of 76% for HDE, and the corresponding RO product as reclaimed water contained only 223 mg·L of TDS, 3.87 mg·mL of DOC and 10.

Biosorption of anionic and cationic dyes raw and chitosan oligosaccharide-modified Huai Flos Chrysanthemum at different temperatures.

Raw Huai Flos Chrysanthemum (HFC) and modified HFC (HFC@CO) were used for the first time as a biosorbent material to remove cationic dyes Malachite green (MG) and Crystal violet (CV), and anionic dyes Sunset yellow (SY), Lemon yellow (LY), and Carmine (CM), at different temperatures (5-50 °C). The highest removal rates () for dye adsorption were observed at low temperature (5 °C) and room temperature (20 °C). At high (500 mg L) dye concentration, adsorption was completed within one minute, but the time required to reach adsorption equilibrium was longer than at the low (20 mg L) concentration.

New Insights into the Role of Al O in the Promotion of CuZnAl Catalysts: A Model Study.

The Cu/Al O /ZnO(0001)-Zn ternary model catalysts and their binary analogues were prepared and characterized. It was found that Al O grew on the ZnO(0001)-Zn surface by a layer-by-layer model, whereas Cu grew on the ZnO(0001)-Zn surface as two-dimensional clusters up to 0.2 monolayers (ML), and thereafter formed three-dimensional clusters.

Photoinduced Formation of Peroxide Ions on La2O3 and Nd2O3 under O2: Effects of Excitation Wavelength and Crystal Structure.

Photoinduced formation of peroxide ions on La2O3 and Nd2O3 under O2 was studied by in-situ microprobe Raman spectroscopy with attention focused on the effect of excitation wavelength and crystal structure on the O2(2-) formation. It was found that photoexcitations at 633, 532, 514, and 325 nm can induce O2(2-) formation over La2O3 at 450 °C. By contrast, photoexcitation at 785 nm does not cause formation of O2(2-) up to 500 °C.

Dimeric 1,3-propanediaminetetraacetato lanthanides as the precursors of catalysts for the oxidative coupling of methane.

From neutral solutions, dimeric 1,3-propanediaminetetraacetato lanthanides (NH4)2[Ln2(1,3-pdta)2(H2O)4]·8H2O [Ln = La, 1; Ce, 2] and K2[Ln2(1,3-pdta)2(H2O)4]·11H2O [Ln = La, 3; Ce, 4] (1,3-H4pdta = 1,3-propanediaminetetraacetic acid, C11H18N2O8) were isolated in high yields. The reaction of excess strontium nitrate with 1 resulted in the formation of a two dimensional coordination polymer [La2(1,3-pdta)2(H2O)4]n·[Sr2(H2O)6]n·[La2(1,3-pdta)2(H2O)2]n·18nH2O (5) at 70 °C. Complexes 1-4 show a similar central molecular structure.

Chemical synthesis of lactic acid from cellulose catalysed by lead(II) ions in water.

The direct transformation of cellulose, which is the main component of lignocellulosic biomass, into building-block chemicals is the key to establishing biomass-based sustainable chemical processes. Only limited successes have been achieved for such transformations under mild conditions. Here we report the simple and efficient chemocatalytic conversion of cellulose in water in the presence of dilute lead(II) ions, into lactic acid, which is a high-value chemical used for the production of fine chemicals and biodegradable plastics.

Synergistic effects of VO(x)-Pt probed by the oxidation of propane on VO(x)/Pt(111).

VO(x)/Pt(111), which was grown layer-by-layer and exhibited a well-defined structure, was used as a model catalytic surface to study the intrinsic catalytic activity of Pt, as well as the effect of VO(x) additive, for the oxidation of propane. A special sample system was designed to ensure a reliable analysis of the trace amount of model catalytic reaction products. The results show that the catalytic activities for the oxidation of C3H8 on the Pt(111) surface as adding VO(x) are suppressed apparently at temperatures below 400 K, but enhanced significantly at temperatures above 400 K.

Effects of O2 pressure on the oxidation of VO(x)/Pt(111).

Vanadium oxide (VO(x)) has been extensively used in many oxidation and selective oxidation reactions. In this study, VO(x) thin films were prepared in an ultra-high vacuum (UHV) chamber by evaporating V onto a Pt(111) surface followed by subsequent oxidation at 623 K in 1 × 10(-7) Torr O2, and further oxidized in the 'high-pressure' reaction cell with 1 Torr O2. The film quality and structure were investigated by high-resolution electron energy loss spectroscopy (HREELS), X-ray photoelectron spectroscopy (XPS), low energy electron diffraction (LEED), low energy ion scattering spectroscopy (LEIS), Auger electron spectroscopy (AES), and in situ infrared reflection absorption spectroscopy (IRAS).

A novel visible-light-response plasmonic photocatalyst CNT/Ag/AgBr and its photocatalytic properties.

A facile, one-step synthesis of carbon nanotube (CNT)-loaded Ag/AgBr is reported. The as-prepared samples were characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), UV/Vis absorption spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, photoluminescence (PL) spectroscopy and electrochemical impedance spectroscopy (EIS). The CNT/Ag/AgBr composite exhibited much higher photocatalytic activity than pure Ag/AgBr in degrading methyl orange (MO) dye solution.

Effect of calcination temperature and pretreatment with reaction gas on properties of Co/γ-Al2O3 catalysts for partial oxidation of methane.

The effects of calcination temperature and feedstock pretreatment on the catalytic performance of Co/γ-Al(2)O(3) catalysts were studied for partial oxidation of methane (POM) to synthesis gas, with emphasis on the role of feedstock pretreatment. The physicochemical properties of the catalysts were characterized by N(2) adsorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), H(2) temperature-programmed reduction (H(2) -TPR), and Raman spectroscopy. The results showed that the pretreatment of the catalyst by reaction gas significantly improved the catalytic activity and stability for the POM reaction.

Mechanistic aspects of photo-induced formation of peroxide ions on the surface of cubic Ln2O3 (Ln = Nd, Sm, Gd) under oxygen.

The photo-induced formation of peroxide ions on the surface of cubic Ln2O3 (Ln = Nd, Sm, Gd) was studied by in situ microprobe Raman spectroscopy using a 325 nm laser as excitation source. It was found that the Raman bands of peroxide ions at 833-843 cm(-1) began to grow at the expense of the Ln(3+)-O(2-) bands at 333-359 cm(-1) when the Ln2O3 samples under O2 were continuously irradiated with a focused 325 nm laser beam at temperatures between 25-150 °C. The intensity of the peroxide Raman band was found to increase with increasing O2 partial pressure, whereas no peroxide band was detected on the Ln2O3 under N2 as well as on the samples first irradiated with laser under Ar or N2 followed by exposure to O2 in the dark.

Synthesis, characterization and photocatalytic property of AgBr/BiPO4 heterojunction photocatalyst.

A novel heterojunction AgBr/BiPO(4) photocatalyst was synthesized with the hydrothermal method. The photocatalyst was characterized by X-Ray powder Diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Spectrometry (EDS), Transmission Electron Microscopy (TEM), X-ray Photoelectron Spectrscopy (XPS) and Diffuse Reflectance Spectroscopy (DRS). The XRD, SEM-EDS, TEM and XPS analyses indicated that the heterojunction structure formed during the process of hydrothermal treatment.

In situ Raman and pulse reaction study on the partial oxidation of methane to synthesis gas over a Pt/Al2O3 catalyst.

Catalytic partial oxidation of methane (POM) to synthesis gas (syngas) over Pt/Al(2)O(3) was investigated by in situ microprobe Raman and pulse reaction methods with attention focused on the mechanism of syngas formation in the oxidation zone (i.e., the catalyst zone in which O(2) was still available in the reaction feed).

Active surfaces for CO oxidation on palladium in the hyperactive state.

Hyperactivity was previously observed for CO oxidation over palladium, rhodium, and platinum surfaces under oxygen-rich conditions, characterized by reaction rates 2-3 orders higher than those observed under stoichiometric reaction conditions [Chen et al. Surf. Sci.

Brønsted-NH(4)(+) mechanism versus nitrite mechanism: new insight into the selective catalytic reduction of NO by NH(3).

The selective catalytic reduction (SCR) of NO by NH(3) over V(2)O(5)-based catalysts is used worldwide to control NO(x) emission. Understanding the mechanisms involved is vital for the rational design of more effective catalysts. Here, we have performed a systematic density functional theory (DFT) study of a SCR reaction by using cluster models.

Polyoxometalate-supported Pd nanoparticles as efficient catalysts for the direct synthesis of hydrogen peroxide in the absence of acid or halide promoters.

A Keggin-type polyoxometalate (Cs(1.5)H(1.5)PW(12)O(40))-supported Pd catalyst is efficient for the direct synthesis of H(2)O(2) from H(2) and O(2) in the absence of any acid or halide additives under atmospheric pressure.

NiO-polyoxometalate nanocomposites as efficient catalysts for the oxidative dehydrogenation of propane and isobutane.

Novel nanocomposites of NiO and polyoxometalate (Cs(2.5)H(0.5)PMo(12)O(40)) with particle sizes in the range of 5-10 nm showed exceptional oxygen and ammonia adsorption capabilities, and the nanocomposites catalyzed the oxidative dehydrogenation of propane and isobutane efficiently under mild conditions.

Mechanisms for O2 dissociation over the BaO (100) surface.

We have investigated the atomic and molecular oxygen adsorptions on the various sites of the BaO (100) surface with both cluster models and the periodic slab models. We found that the atomic oxygen prefers to adsorb on the surface O2- to form the closed-shell peroxides with the binding energies of 83-88 kcal/mol. Such a high exothermicity provides a large driving force for the dissociation of molecular O2 on the BaO surfaces.