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Glutaraldehyde non-conjugated chitosan polymer fluorophores for selective determination of picric acid via fluorescence resonance energy transfer strategy
摘要： Water-dispersed glutaraldehyde (GA) non-conjugated chitosan polymer fluorophores (GCPF) with quantum yield of 16 % is synthesized by stirring chitosan and GA for 6 h at room temperature in the present work. It is a facile and mild method and fluorescent GCPF can be stabled for two months. Owing to the spectral overlap of fluorescent spectrum of GCPF and absorption spectrum of picric acid (PA), a novel sensitive fluorescent method using fluorescent GCPF for PA detection from 10 nM to 50 μM via fluorescence resonance energy transfer (FRET) strategy is established. The distance between donor of GCPF and acceptor of PA (R0 value) is calculated to be 3.5 nm. FRET method using fluorescent GCPF possesses high sensitivity (LOD of 2.8 nM), and selectivity and fast response within 2 min. Moreover, fluorescent GCPF is also utilized in visual analysis of PA using cotton swabs. Fluorescence quenching effect can be observed by eyes irradiated with 365 nm ultraviolet light at cotton swabs and using GCPF solid on quartz glasses, which paves an effect and wide way for the application of fluorescent GCPF in our daily life.
关键词： Glutaraldehyde non-conjugated chitosan polymer fluorophores (GCPF),picric acid (PA),fluorescence resonance energy transfer (FRET),glutaraldehyde (GA),chitosan
更新于2025-11-14 15:23:50
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Study of visible-light photocatalytic degradation of 2,4-dichlorophenoxy acetic acid in batch and circulated-mode photoreactors
摘要： Purpose The consumption of pesticides and chemical fertilizers is one of the major environmental and health problems. In this report, 2,4-dichlorophenoxyacetic acid (2,4-D) was chosen to evaluate the impact of photodegradation using LED (Light-emitting diode) (400 and 365 nm) sources in batch and programmable circulated-mode photoreactors respectively. Methods A β-cyclodextrin (β-CD) grafted titanium dioxide P25 (P25/β-CD) and complexation of 2,4-D and β-CD were synthesized via photoinduced and spray-drying methods, respectively. The structures were characterized. Moreover, we investigated the effects of the amount of catalyst, the β-CD amount on bed catalyst, irradiation time, kind of photoreactor on the photocatalytic degradation efficiency. Results Based on the results of experiments in batch reactor, the optimum amount of TiO2, β-CD grafted by catalyst were 1 and 0.1 g/L, respectively. In batch-mode the photodegradation efficiency of 2,4-D after 5 h with P25, P25/β-CD as a photocatalyst and 2,4-D/β-CD complex with P25 photocatalyst were approximately 81, 85 and 95% respectively. After 8 h of irradiation in circulated-mode reactor, degradation yields with P25, P25/β-CD and 2,4-D/β-CD complex along with P25 were 89, 91 and 96% respectively. On the other hand, the circulated-mode photoreactor with high efficiency was appropriate to degradation of the high concentration of 2,4-D solution (200 mg/L). After 5 successive cycles with 25 h of irradiation, P25 and P25/β-CD maintained as high 2,4-D removal efficiency as 82.6, 84% respectively, with excellent stability and reusability. Conclusion The photodegradation method can be used as an effective and environmental friendly process in the degradation of organic compound.
关键词： 2,4-D/β-CD complex,Batch-mode photoreactor,Light-emitting diode (LED),Circulated-mode photoreactor,2,4-Dichlorophenoxyacetic acid (2,4-D)
更新于2025-11-14 15:18:02
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Efficient visible light driven degradation of sulfamethazine and tetracycline by salicylic acid modified polymeric carbon nitride via charge transfer
摘要： Photocatalysis has been widely studied as a promising technique for removal of organic pollutants in wastewater. A modified carbon nitride has been designed for this purpose. In this study, a facile method to synthesize distorted carbon nitride by simply copolymerizing urea and salicylic acid (SA) has been explored. The incorporation of SA induced the structure change from planar structure to distorted curls structure. Compared to pristine CN, the CN-SA shows wide light absorption, which is attributed to the n → π* transition at the nitrogen atoms with lone pair electrons of heptazine units. The photoelectrode of CN-SA exhibited higher photocurrent and lower charge resistance than that of pristine CN electrode, indicating that the photogenerated charge carriers of CN-SA are more efficiently separated. As a result, the optimal CN-SA shows 2-fold enhancement in degradation of tetracycline (TC) as compared to pristine CN. Furthermore, we found that the degradation rate of sulfamethazine (SMZ) was 0.0823 min?1 using the CN-SA photocatalyst, which is three times higher than that of pristine CN (0.0293 min?1). In addition, the CN-SA shows good stability without structural change or loss of photocatalytic performance after four cycles. According to the radical species trapping experiments and electron spin resonance analyses, ?O2? and h+ were the main active species involved in the degradation of organic pollutants. The developed strategy provides a novel approach to design the tunable band structure of organic semiconductor materials for various applications.
关键词： Salicylic acid,Photocatalysis degradation,Carbon nitride,Charge separation,Antibiotics
更新于2025-11-14 14:48:53
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Spectroscopic and theoretical studies of potassium sodium l-(+)-tartrate tetrahydrate and l-tartaric acid used as precursors for in situ laser-induced deposition of the catalytically active copper microstructures
摘要： In this work we study the influence of l-(+)-КNaC4H4O6 × 4H2O (KNaT) and l-H2C4H4O6 (H2T) on the complexation processes occurring during in situ laser-induced catalytic destruction of the organic components of the aqueous solutions with formation of the unsaturated hydrocarbons. For that purpose, ATR-FTIR, Raman, IR, and NIR spectroscopy as well as quantum chemical calculations were implemented. It was observed that hydration of T2? anion via carboxylate groups is stronger than that via hydroxyl groups. We also established the changes in the spectral characteristics of the absorption bands corresponding to vibrations of T2?, HT?, and H2T, at solid state-liquid and acid-salt transitions, depending on concentration of the solution components and the [OH?]/[H2T] ratio. Finally, it was shown that ethylene is a main product of the catalytic destruction of the copper tartrate complexes.
关键词： IR,Laser-induced copper deposition,DFT calculations,Tartaric acid,ATR-FTIR,Catalysis,NIR,Raman spectroscopy,Sodium potassium tartrate tetrahydrate
更新于2025-10-22 19:40:53
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Eumelanin for Nature‐Inspired UV‐Absorption Enhancement of Plastics
摘要： In the human body, the black-brown biopigment eumelanin blocks the harmful ultraviolet (UV) radiation. In the plastics industry, additives are often added to polymers to increase their UV-absorption properties. We herein report an assessment of the biopigment eumelanin as a nature-inspired additive for plastics to enhance their UV-absorption. Since eumelanin is produced by natural sources and is non-toxic, it is an interesting candidate in the field of sustainable plastic additives. In this work, eumelanin-including films of commercial ethylene-vinyl acetate copolymer (EVA), a plastic used for packaging applications, were obtained by melt-compounding and compression molding. The biopigment dispersion in the films was improved by means of the Melanin Free Acid treatment (MFA). It was observed that eumelanin amounts as low as 0.8% wt. cause an increase of the UV absorption, up to one order of magnitude in the UVA range. We also evaluated the effect of eumelanin on the thermal and photostability of the films: the biopigment proved to be double-edged, working both as UV-absorption enhancer and photo-prooxidant, as thermogravimetric analysis (TGA) and infrared (IR) spectroscopy revealed.
关键词： Eumelanin,Packaging,Melanin Free Acid,UV-absorbers,Ethylene-vinyl acetate copolymer,UV-aging
更新于2025-10-22 19:40:53
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Diode Array Near Infrared Spectrometer Calibrations for Composition Analysis of Single Plant Canola (Brassica napus) Seed
摘要： A canola breeder needs an accurate, rapid, non-destructive method for analyzing seeds from a single plant to select the most promising samples for further breeding trials. Near Infrared Spectroscopy (NIRS) is widely used for quantitative analysis of oilseeds in a non-destructive manner. This research was aimed at developing NIRS calibration models for single plant canola seed using a diode array NIRS (950-1650 nm wavelength range), multivariate prediction models, and a mirrored sample cup. Eighteen different NIRS calibration models were developed using 100 samples for each constituent with different pre-processing techniques (mean center, derivatives, variates) and models (PLS, PCR). The relative performance of different calibration models for each constituent was compared using R2, SEP, and ratio performance deviation (RPD) values obtained from the validation set of 30 samples. NIRS models developed using the PLS regression algorithm for moisture content (R2 = 0.97, SEP = 0.32, RPD = 6.13) and oil content (R2 = 0.84, SEP = 0.61, RPD = 4.16) were successful. However, acceptable NIRS models were not obtained for fatty acid and glucosinolates content likely due to limited variability and low levels of the constituent and a narrow wavelength range of the DA-NIR instrument.
关键词： Moisture content,Diode array,Fatty acid composition,Mirrored cup,DA-NIRS,Oil content,Oleic acid,Stearic acid,NIRS calibration model,Palmitic acid
更新于2025-09-23 15:23:52
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Photodynamic Therapy in the Treatment of Bladder Cancer: Past Challenges and Current Innovations
摘要： There are limited treatment options for patients with recurrent non-muscle-invasive bladder cancer. In this report, we will talk about the history of photodynamic therapy; although it showed encouraging therapeutic results, it was largely abandoned due to toxicity or bystander effects on normal cells. Monoclonal antibody-conjugates represent an emerging therapeutic approach for malignancies that improves upon tumor specificity. The use of a monoclonal antibody-photosensitizer conjugate is a more selective method of delivering light therapy and has been termed 'photoimmunotherapy', which we will discuss in the last part of this report.
关键词： Hematoporphyrin,Urothelial cancer,Hexaminolevulinic acid,Photoimmunotherapy,PIT,BCG-refractory NMIBC,PDT,Bladder cancer,5-Aminolevulinic acid,Photodynamic therapy
更新于2025-09-23 15:23:52
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Suppression of riboflavin-sensitized singlet oxygen generation by l-ascorbic acid, 3-O-ethyl-l-ascorbic acid and Trolox
摘要： Riboflavin (RF), a water-soluble vitamin B2, is an endogenous singlet oxygen photosensitizer in human skin and eye. Time profiles of the near-infrared phosphorescence of singlet oxygen generated by RF have been measured in the absence and presence of L-ascorbic acid (AA, vitamin C), 3-O-ethyl-L-ascorbic acid (3-EtAA) and Trolox (TX, a water-soluble analogue of vitamin E) in phosphate buffer (pH 6.8). These substances suppress the RF-photosensitized singlet oxygen generation. For example, the quantum yield of singlet oxygen generation is decreased to a third by adding 0.4 mmol dm?3 AA or TX (the concentration of dissolved oxygen in air-saturated water is 0.27 mmol dm?3). AA and TX are more efficient suppressors of RF-photosensitized singlet oxygen generation than 3-EtAA. The bimolecular rate constants for quenching of the excited singlet and triplet states of RF by AA, 3-EtAA and TX have been determined through measurements of fluorescence and transient absorption. These measurements suggest that the observed suppression is due to the quenching of the excited singlet and triplet states of RF by AA, 3-EtAA and TX. The bimolecular rate constants for quenching of singlet oxygen by AA, 3-EtAA and TX were determined to be 1.8 × 108, 0.27 × 108, and 4.4 × 108 mol?1 dm3 s?1, respectively.
关键词： Trolox,Riboflavin,Singlet oxygen,3-O-ethyl-L-ascorbic acid,L-ascorbic acid
更新于2025-09-23 15:23:52
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Night-Time Oxidation of a Monolayer Model for the Air–Water Interface of Marine Aerosols—A Study by Simultaneous Neutron Reflectometry and in Situ Infra-Red Reflection Absorption Spectroscopy (IRRAS)
摘要： This paper describes experiments on the ageing of a monolayer model for the air–water interface of marine aerosols composed of a typical glycolipid, galactocerebroside (GCB). Lipopolysaccharides have been observed in marine aerosols, and GCB is used as a proxy for these more complex lipopolysaccharides. GCB monolayers are investigated as pure films, as mixed films with palmitic acid, which is abundant in marine aerosols and forms a stable attractively mixed film with GCB, particularly with divalent salts present in the subphase, and as mixed films with palmitoleic acid, an unsaturated analogue of palmitic acid. Such mixed films are more realistic models of atmospheric aerosols than simpler single-component systems. Neutron reflectometry (NR) has been combined in situ with Fourier transform infra-red reflection absorption spectroscopy (IRRAS) in a pioneering analysis and reaction setup designed by us specifically to study mixed organic monolayers at the air–water interface. The two techniques in combination allow for more sophisticated observation of multi-component monolayers than has previously been possible. The structure at the air–water interface was also investigated by complementary Brewster angle microscopy (BAM). This study looks specifically at the oxidation of the organic films by nitrate radicals (NO3?), the key atmospheric oxidant present at night. We conclude that NO3? oxidation cannot fully remove a cerebroside monolayer from the surface on atmospherically relevant timescales, leaving its saturated tail at the interface. This is true for pure and salt water subphases, as well as for single- and two-component films. The behaviour of the unsaturated tail section of the molecule is more variable and is affected by interactions with co-deposited species. Most surprisingly, we found that the presence of CaCl2 in the subphase extends the lifetime of the unsaturated tail substantially—a new explanation for longer residence times of materials in the atmosphere compared to lifetimes based on laboratory studies of simplified model systems. It is thus likely that aerosols produced from the sea-surface microlayer at night will remain covered in surfactant molecules on atmospherically relevant timescales with impact on the droplet’s surface tension and on the transport of chemical species across the air–water interface.
关键词： palmitic acid,monolayer,neutron,nitrate radical,palmitoleic acid,reflectivity,aerosol,infra-red,cerebroside,Brewster angle microscopy
更新于2025-09-23 15:23:52
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Modulation the electronic property of 2D monolayer MoS2 by amino acid
摘要： 2D molybdenum disulfide (MoS2) has a strong potential for the detection of biomolecules, however, the specific interactions between individual amino acids and MoS2 surface are still unclear. Herein, the adsorption properties and electronic structures of amino acid/MoS2 systems were investigated systematically for the 20 standard amino acids based on density functional theory. The adsorption strength of amino acids on MoS2 monolayer decreases in the following order: TRP > ARG > PHE > TYR > LYS > HIS > PRO > ASN > MET > LEU > ILE > VAL > GLU > GLN > THR > ASP > CYS > SER > ALA > GLY. The band gap of amino acid/MoS2 system is determined by the energy level of HOMO orbit of the adsorbed amino acid, in which the higher energy level of HOMO orbit will result in a smaller band gap. As proof of concept, optical and electrical detection of the MoS2 based transistors with and without amino acid molecules (TRP and CYS) were studied. Adsorption of amino acids on a MoS2 surface allows their chemical information to be transformed into distinct analytically optical and electronic signals, which opens up new possibilities for fabricating novel MoS2 based highly selective biosensors.
关键词： Amino acid,MoS2,Density functional theory,Field effect transistors
更新于2025-09-23 15:23:52