98%
921
2 minutes
20
The unprecedented use of high-resolution continuum source molecular absorption spectrometry (HR-CS MAS) for the fractionation of organic and inorganic sulfur (S) species through monitoring the CS molecule is presented here. Two separate methods for determining organic (CS) and inorganic (CS) sulfur were developed to work sequentially. The optimized temperature program for both methodologies has two pyrolysis steps and one vaporization step (1st T: 1800 and 2T: 800 °C, and T: 2500 °C). The fractionation was achieved by implementing hydrophobic Pd NPs and Ca as chemical modifiers for the CS and CS methods. Method development was performed by applying different statistical models, allowing the definition of optimal conditions for the chemical modifier mass, and minimizing the S species interconversion, i.e., Doehlert design, and central composite design. The limits of detection (LoD) for CS and CS were 2.4 and 2.1 mg L, respectively. Recovery tests evaluated the method's specificity and accuracy; over 92 % recovery was found for both CS and CS. Thus, the proposed methods offer a reliable alternative for fractionating organic and inorganic S by using HR-CS MAS.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.talanta.2024.126694 | DOI Listing |
Commun Chem
September 2025
Dresden Integrated Center for Applied Physics and Photonic Materials (IAPP), Technische Universität Dresden, Dresden, Germany.
Purely organic materials showing efficient and persistent emission via room temperature phosphorescence (RTP) allow the design of minimalistic yet powerful technological solutions for sensing, bioimaging, information storage, and safety applications using the photonic design principle of digital luminescence. Although several promising materials exist, a deep understanding of the underlying structure-property relationship and, thus, development of rational design strategies are widely missing. Some of the best purely organic emitters follow the donor-acceptor-donor design motif.
View Article and Find Full Text PDFBioresour Technol
September 2025
Research Division for Water Environmental Science and Engineering, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China. Electronic address:
Constructed wetlands (CWs) treating nitrate-rich wastewater often face incomplete denitrification and elevated NO emissions due to insufficient electron donors. Pyrrhotite as a CW substrate demonstrated potential for enhancing autotrophic denitrification through coupled sulfur and iron biological oxidation. However, the impact of pyrrhotite layer positioning on regulating NO emissions and underlying mechanisms remains unclear.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua 321004, China.
Room-temperature crystallization of a cobalt-aminoterephthalate framework (CoBDC-NH) directly on 3D-printed polylactic acid (PLA) yields a super-wetting membrane that reconciles permeability and selectivity in oil-water separation. The ambient-pressure route dispenses with conventional hydrothermal steps and preserves the PLA architecture. Molecular dynamics (MD) combined with density-functional (DFT) calculations reveal that NaOH activation exposes carboxylate sites, while trace polyvinylpyrrolidone amplifies van der Waals forces, uniformly dispersing Co nuclei and anchoring the metal-organic framework (MOF) layer.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
College of Materials Science and Engineering, Sichuan University, No. 24 South Section 1, Yihuan Road, Chengdu 610065, P. R. China.
Aqueous zinc-ion microbatteries exhibit promising prospects for wearable devices due to their high safety and cost-effectiveness but face challenges such as low energy density and short cycle life. To address these challenges, a dual-plating flexible Zn-Br microbattery was developed using freestanding MXene films as a zinc metal free anode. The MXene anode retains no redundant Zn, as Zn from the electrolyte undergoes deposition/stripping reactions on its substrate, thereby eliminating the necessity for excess zinc.
View Article and Find Full Text PDFLangmuir
September 2025
Laboratory of Electrochemistry-Corrosion, Metallurgy and Inorganic Chemistry, Faculty of Chemistry, USTHB, BP 32, 16111, Algiers, Algeria.
Azo dyes, prevalent in various industries, including textile dyeing, food, and cosmetics, pose significant environmental and health risks due to their chemical stability and toxicity. This study introduces the synthesis and application of a copper hydrogen-π-bonded benzoate framework (Cu-HBF) and its derived marigold flower-like copper oxide (MFL-CuO) in a synergetic adsorption-photocatalytic process for efficiently removing cationic azo dyes from water, specifically crystal violet (CV), methylene blue (MB), and rhodamine B (RhB). The Cu-HBF, previously available only in single crystal form, is prepared here as a crystalline powder for the first time, using a low-cost and facile procedure, allowing its application as an adsorbent and also serving as a precursor for synthesizing well-structured copper oxide (MFL-CuO).
View Article and Find Full Text PDF