Novel CuMgAlTi-LDH Photocatalyst for Efficient Degradation of Microplastics under Visible Light Irradiation.

Microplastics (MPs) in the water system could easily enter the human body and pose a potential threat, so finding a green and effective solution remains a great challenge. At present, the advanced oxidation technology represented by photocatalysis has been proven to be effective in the removal of organic pollutants, making it a feasible method to solve the problem of MP pollution. In this study, the photocatalytic degradation of typical MP polystyrene (PS) and polyethylene (PE) by a new quaternary layered double hydroxide composite photomaterial CuMgAlTi-R400 was tested under visible light irradiation. After 300 h of visible light irradiation, the average particle size of PS decreased by 54.2% compared with the initial average particle size. The smaller the particle size, the higher the degradation efficiency. The degradation pathway and mechanism of MPs were also studied by GC-MS, which showed that PS and PE produced hydroxyl and carbonyl intermediates in the process of photodegradation. This study demonstrated a green, economical, and effective strategy for the control of MPs in water.

Wafer-scale nanostructured black silicon with morphology engineering via advanced Sn-assisted dry etching for sensing and solar cell applications.

Black-Si (b-Si) providing broadband light antireflection has become a versatile substrate for photodetectors, photo-electric catalysis, sensors, and photovoltaic devices. However, the conventional fabrication methods suffer from single morphology, low yield, or frangibility. In this work, we present a high-yield CMOS-compatible technique to produce 6-inch wafer-scale b-Si with diverse random nanostructures. b-Si is achieved by O2/SF6 plasma-based reactive ion etching (RIE) of the Si wafer which is coated with a GeSn layer. A stable grid of the SnOxFy layer, formed during the initial GeSn etching, acts as a self-assembled hard mask for the formation of subwavelength Si nanostructures. b-Si wafers with diverse surface morphologies, such as the nanopore, nanocone, nanohole, nanohillock, and nanowire were achieved. Furthermore, the responsivity of the b-Si metal-semiconductor-metal (MSM) photodetector in the near-infrared (NIR) wavelength range (1000-1200 nm) is 40-200% higher than that of a planar-Si MSM photodetector with the same level of dark current, which is beneficial for applications in photon detectors, solar cells, and photocatalysis. This work not only demonstrates a new non-lithography method to fabricate wafer-scale b-Si wafers, but may also provide a novel strategy to fabricate other nanostructured surface materials (e.g., Ge or III-V based compounds) with morphology engineering.

Visible-light photoelectrocatalysis/H2O2 synergistic degradation of organic pollutants by a magnetic Fe3O4@SiO2@mesoporous TiO2 catalyst-loaded photoelectrode.

In this paper, we describe a method for photoelectrocatalysis (PEC)/H2O2 synergistic degradation of organic pollutants with a magnetic Fe3O4@SiO2@mesoporous TiO2 (FST) photocatalyst-loaded electrode. At optimal conditions of pH 3.0, 2.25% H2O2, working electrode (fixed FST 30 mg) potential +0.6 V (vs. SCE), and 10 mg L-1 of all experimental pollutants, the FST PEC/H2O2 synergistic system exhibited high activity and stability for the removal of various organic pollutants under visible light with comparable degradation efficiencies, including MB (98.8%), rhodamine B (Rh B, 96.7%), methyl orange (MO, 97.7%), amoxicillin (AMX, 83.9%). Moreover, this system obtained TOC removal ratios of 83.5% (MB), 77.9% (Rh B), 80.2% (MO), 65.5% (AMX) within 8 min. The kinetic rate constants of the PEC/H2O2 synergistic system were nearly 53 and 1436 times higher than that of the PEC process and H2O2 photolysis under visible light, respectively. Furthermore, the main reactive oxidant species (˙OH, ˙O2 -) were studied and enhanced mechanisms of the photocatalytic-electro-H2O2 coupling system were proposed. This work brings new insights to efficiently purify organic pollutants by PEC coupled with peroxide under solar light illumination.

In Situ Chemical Modification with Zwitterionic Copolymers of Nanofiltration Membranes: Cure for the Trade-Off between Filtration and Antifouling Performance.

Breaking the trade-off between filtration performance and antifouling property is critical to enabling a thin-film nanocomposite (TFC) nanofiltration (NF) membrane for a wide range of feed streams. We proposed a novel design route for TFC NF membranes by grafting well-defined zwitterionic copolymers of [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (SBMA) and 2-aminoethyl methacrylate hydrochloride (AEMA) on the polyamide surfaces via an in situ surface chemical modification process. The successful grafting of a zwitterionic copolymer imparted the modified NF membranes with better surface hydrophilicity, a larger actual surface area (i.e., nodular structures), and a thinner polyamide layer. As a result, the water permeability of the modified membrane (i.e., TFC-10) was triple that of the pristine TFC membrane while maintaining high Na2SO4 rejection. We further demonstrated that the TFC-10 membrane possessed exceptional antifouling properties in both static adsorption tests and three cycles of dynamic protein and humic acid fouling tests. To recap, this work provides valuable insights and strategies for the fabrication of TFC NF membranes with simultaneously enhanced filtration performance and antifouling property.

Bioremediation of oil contaminated soil using agricultural wastes via microbial consortium.

Agricultural wastes, such as wheat bran and swine wastewater, were used for bioremediation of oil-contaminated soil. Two optimised strains that could degrade oil efficiently were selected. The result showed that the best ratio of strain A to strain B was 7:3. Swine wastewater could be a replacement for nitrogen source and process water for bioremediation. Next, the Box-Behnken design was used to optimise the culture medium, and the optimal medium was as follows: microbial dosage of 97 mL/kg, wheat bran of 158 g/kg and swine wastewater of 232 mL/kg. Under the optimal medium, the oil degradation rate reached 68.27 ± 0.71% after 40 d. The urease, catalase, and dehydrogenase activities in oil-contaminated soil all increased, and the microbe quantity increased significantly with manual composting. These investigations might lay a foundation for reducing the pollution of agricultural wastes, exploring a late model for bioremediation of oil-contaminated soil.

Economical production of vitamin K2 using crude glycerol from the by-product of biodiesel.

Industrial waste, such as crude glycerol, was used for vitamin K2 by B. subtilis Z-15. Crude glycerol could be used instead of pure glycerin for vitamin K2 production. The combination of soybean peptone and yeast extract was more conducive to the synthesis of vitamin K2. The optimal composition of medium was obtained by response surface methodology. The results indicated that the optimal medium was as follows: 6.3% crude glycerol, 3.0% soybean peptone concentration and 5.1 g/L yeast extract. Under the optimal culture medium, vitamin K2 production was increased to 45.11 ± 0.62 mg/L. The fermentor test further proved that the use of crude glycerol affected neither the synthesis of vitamin K2 nor the growth of B. subtilis. These investigations could lay a foundation for reducing the pollution of crude glycerol, exploring a late model for vitamin K2 cleaner production.

Biosorption of Cr(VI) by immobilized waste biomass from polyglutamic acid production.

Waste biomass from γ-polyglutamic acid production was used as an adsorbent to remove Cr(VI) from wastewater. Waste biomass was entrapped in sodium alginate to enhance performance. Orthogonal array design was used to optimize biosorption of Cr(VI) by immobilized waste biomass. The optimal adsorption conditions for immobilized waste biomass were as follows: pH 7.0, initial Cr(VI) concentration of 200 mg/L, 35 °C, waste biomass of 2 g/L, 60 min. Under these conditions, the absorption efficiency of Cr(VI) was 96.38 ± 0.45%. When the waste biomass was treated with 1 mol/L HCl for 1 h, the desorption rate could reach 94.42 ± 0.87%. It was shown that the adsorption kinetics followed the Freundlich adsorption model, indicating that the adsorption of Cr(VI) by bacteria was mainly based on multi-molecular layer adsorption. The absorption conditions of waste biomass were mild (pH 6.0-7.5, 20-35 °C) and easily operated. These investigations lay a foundation for reducing the pollution of γ-polyglutamic acid production, turning the biomass waste into a useful adsorbent for wastewater treatment.

Production of ethanol from Jerusalem artichoke by mycelial pellets.

Mycelial pellets formed by Aspergillus niger A-15 were used to immobilize the ethanol producing yeast Saccharomyces cerevisiae C-15. The operation parameters, such as agitation speed, temperature and mixed proportion of strains were studied. The optimal adsorption 66.9% was obtained when speed was 80r/min, temperature was 40 °C and mixed proportion(mycelial pellets: yeasts) was 1:10. With Jerusalem artichoke flour as substrate, 12.8% (V/V) of ethanol was obtained after 48 h by simultaneous saccharification and fermentation using mycelial pellets. And mycelial pellets could tolerate 19% (volume fraction) ethanol. The above results proved that this new technology was feasible, and it had the advantages of higher ethanol yield, long service life, repeated use, easy operation and lower cost in producing ethanol.

Efficient lead ion removal from water by a novel chitosan gel-based sorbent modified with glutamic acid ionic liquid.

Three novel and highly effective AAIL-modified Chitosan (CS) adsorbents are presented. These three new CS-gels were prepared by an innovative synthetic method that uses amino acid ionic liquids (AA-ILs) to cross-link CS with, separately, glutamic acid, aspartic acid and alanine to give novel adsorbents Glu-AA-IL-CS (1), Asp-AA-IL-CS (2) and Ala-AA-IL-CS (3) respectively. The effectively incarcerating host-structures (1) - (3) were characterized by a whole range of techniques including FT-IR, SEM, EDS and XRD. The differences amongst novel adsorbents (1) - (3) with regard to their rate and efficiency of removal of Pb2+ from aqueous solutions are explained in terms of the different electronic, structural and steric features of the three amino acids. The glutamic acid variant (1) is clearly shown to be the best-performing adsorbent by experimental tests and data in combination with infrared spectroscopy. The behaviour of adsorbents (1) follows pseudo-second-order kinetics,and accord best with the Freundlich adsorption isotherm.

Efficient Pb(II) removal using sodium alginate-carboxymethyl cellulose gel beads: Preparation, characterization, and adsorption mechanism.

Alginate-carboxymethyl cellulose (CMC) gel beads were prepared in this study using sodium alginate (SA) and sodium CMC through blending and cross-linking. The specific surface area and aperture of the prepared SA-CMC gel beads were tested. The SA-CMC structure was characterized and analyzed via infrared spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. Static adsorption experiment demonstrated that Pb(II) adsorption of SA-CMC exceeded 99% under the optimized conditions. In addition, experiments conducted under the same experimental conditions showed that the lead ion removal efficiency of SA-CMC was significantly higher than that of conventional adsorbents. The Pb(II) adsorption process of SA-CMC followed the Langmuir adsorption isotherm, and the dynamic adsorption model could be described through a pseudo-second-order rate equation. Pb(II) removal mechanisms of SA-CMC, including physical, chemical, and electrostatic adsorptions, were discussed based on microstructure analysis and adsorption kinetics. Chemical adsorption was the main adsorption method among these mechanisms.

A water-soluble fluorescent pH probe based on perylene dyes and its application to cell imaging.

A fluorescent pH probe, N,N'-bi( l-phenylalanine amine)-perylene-3,4;9,10-dicarboxylic diimide (PDCDA) was synthesized and used for pH sensing in living cells. A significant fluorescence intensity change was observed over a pH range from 7.0 to 4.0. Electrostatic potential maps (MEP) suggested that the electronic repulsion between PDCDAs was increased by the high negative electrostatic potential which resulted in a high water solubility of PDCDA. PDCDA was successfully applied as a high-performance fluorochrome for living HeLa cell imaging. The results demonstrate that the probe PDCDA is a good candidate for monitoring pH fluctuations in living cells with good water solubility, low cytotoxicity, high fluorescence quantum yield and photostability.

Iron(II)-dependent dioxygenase and N-formylamide deformylase catalyze the reactions from 5-hydroxy-2-pyridone to maleamate.

5-Hydroxy-2-pyridone (2,5-DHP) is a central metabolic intermediate in catabolism of many pyridine derivatives, and has been suggested as a potential carcinogen. 2,5-DHP is frequently transformed to N-formylmaleamic acid (NFM) by a 2,5-DHP dioxygenase. Three hypotheses were formerly discussed for conversion of 2,5-DHP to maleamate. Based on enzymatic reactions of dioxygenase (Hpo) and N-formylamide deformylase (Nfo), we demonstrated that the dioxygenase does not catalyze the hydrolysis of NFM but rather that this activity is brought about by a separate deformylase. We report that the deformylase acts both on NFM and its trans-isomer, N-formylfumaramic acid (NFF), but the catalytic efficiency of Nfo for NFM is about 1,400 times greater than that for NFF. In addition, we uncover catalytic and structural characteristics of the new family that the Hpo belongs to, and support a potential 2-His-1-carboxylate motif (HX52HXD) by three-dimensional modeling and site-directed mutagenesis. This study provides a better understanding of 2,5-DHP catabolism.

Genome sequence of a nicotine-degrading strain of Arthrobacter.

We announce a 4.63-Mb genome assembly of an isolated bacterium that is the first sequenced nicotine-degrading Arthrobacter strain. Nicotine catabolism genes of the nicotine-degrading plasmid pAO1 were predicted, but plasmid function genes were not found. These results will help to better illustrate the molecular mechanism of nicotine degradation by Arthrobacter.

Dichlorido[2-(3,5-dimethyl-1H-pyrazol-1-yl-κN)-1,10-phenanthroline-κN,N']cadmium(II).

The asymmetric unit of the title compound, [CdCl(2)(C(17)H(14)N(4))], contains two independent mol-ecules in which the Cd(II) ions are in distorted trigonal-bipyramidal CdN(3)Cl(2) coordination environments. In the crystal structure, there is a π-π stacking inter-action involving a pyridine ring and a symmetry-related benzene ring, with a centroid-centroid distance of 3.5088 (19) Å.

NMR study on (+/-)-1-[3-(2-methoxyphenoxy)-2-hydroxypropyl]-4-[(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine dihydrochloride salt.

(+/-)-1-[3-(2-Methoxyphenoxy)-2-hydroxypropyl]-4-[(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine dihydrochloride salt was studied spectroscopically. Complete NMR assignments for dihydrochloride salt were made using DEPT, H-H COSY, as well as HMQC and HMBC heteronuclear correlation techniques.

IR, MS studies on (+/-)-1-[3-(2-methoxyphenoxy)-2-hydroxypropyl]-4-[(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine dihydrochloride salt.

The vibration spectrum and FAB mass spectrum of (+/-)-1-[3-(2-methoxyphenoxy)-2-hydroxypropyl]-4-[(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine dihydrochloride salt was studied. By comparing with the spectra of free base, different bands of IR were found in the NH+ stretching, the NH+ deformation motion, the CH2 of NCH2 group symmetric stretching, the CH2 of N-CH2 group twisting and the CN stretching. FAB shows the basic peak is M + H. Other m/e peaks are consistent with the structure.