Electrostatic Trap Research Articles

A Comparative Study of the Chemical Composition and Skincare Activities of Red and Yellow Ginseng Berries.

This study was conducted to investigate the differences in chemical composition between red (RGBs) and yellow ginseng berries (YGBs) and their whitening and anti-aging skincare effects. The differences in the chemical composition between RGB and YGB were analyzed by ultra-high-performance liquid chromatography tandem quadrupole electrostatic field orbit trap mass spectrometry (UHPLC-Q-Exactive-MS/MS) combined with multivariate statistics. An aging model was established using UVB radiation induction, and the whitening and anti-aging effects of the two ginseng berries were verified in vitro and in vivo using cell biology (HaCaT and B16-F10 cells) and zebrafish model organisms. A total of 31 differential compounds, including saponins, flavonoids, phenolic acids, and other chemical constituents, were identified between the two groups. Superoxide dismutase (SOD) activity was more significantly increased (p < 0.05) and malondialdehyde (MDA) content was more significantly decreased (p < 0.01) in RGB more than YGB induced by UVB ultraviolet radiation. In terms of whitening effects, YGB was more effective in inhibiting the melanin content of B16-F10 cells (p < 0.01). The results of zebrafish experiments were consistent with those of in vitro experiments and cell biology experiments. The DCFH fluorescence staining results revealed that both ginseng berries were able to significantly reduce the level of reactive oxygen species (ROS) in zebrafish (p < 0.01). Comparison of chemical composition and skin care activities based on RGB and YGB can provide a theoretical basis for the deep development and utilization of ginseng berry resources.

Tracking the Molecular-Scale Mechanistic Pathway of Trapping-Bonding CTAB/Fe3O4-AS for High-Performance Cr(VI) Adsorption

Cr(VI) contamination threatens the environment and health, necessitating urgent, sustainable removal solutions. Composite biological adsorbents are promising, yet the molecular-level adsorption mechanisms remain unclear. This gap in understanding hinders the development and application of more efficient biological adsorbent materials. Here, we propose a magnetic composite adsorbent based on Aspergillus niger spores (CTAB/Fe3O4-AS) to track the trapping-bonding mechanisms of Cr(VI) on its surface. Characterization analysis showed that Fe3O4 nanoparticles and CTAB form a stable magnetic shell and an outermost quaternary ammonium layer on the spore surface. This synergistic structure enhanced the Cr(VI) adsorption capacity to 186 mg·g−1 at pH 2.0 in solution and achieved a Cr(VI) removal rate exceeding 99 % in electroplating wastewater, with dosage of 1.8 g·L−1 after 180 min. CTAB/Fe3O4-AS selectively removes Cr(VI) from acidic wastewater, with selectivity coefficients of KCr/Zn = 1334 and KCr/Cu = 2661. Cr(VI) removal occurs mainly through chemical adsorption via heterogeneous processes. DFT calculations and MD simulations visualize reaction pathways and interaction strengths at the molecular scale. The quaternary ammonium cation group ((CH3)4-N+) in CTAB traps Cr(VI) ions electrostatically, transferring them to the spore surface. Electron-donating groups (–COO, –NH-) on the spores reduce Cr(VI) to Cr(III). Amide groups in chitin create optimal coordination sites for Cr(III) by twisting, with nitrogen atoms forming stable complexes through coordination bonds with Cr(III)’s vacant orbitals. This study not only developed an efficient microbial-based composite adsorbent but also proposed a novel synergistic adsorption mechanism: electrostatic trapping–reduction–coordination bonding. This provides valuable insights for developing more efficient and applicable heavy metal ion adsorbent materials in the future.

Realization of Higher Resolution Charge Detection Mass Spectrometry.

Charge detection mass spectrometry (CD-MS) allows mass distributions to be measured for heterogeneous samples that cannot be analyzed by conventional MS. With CD-MS, the m/z and charge are measured for individual ions using a detection cylinder embedded in an electrostatic linear ion trap (ELIT). Imprecision in both the m/z and charge measurements contribute to the mass resolution. However, if the charge can be measured with a precision of <0.2 e the charge state can be assigned with a low error rate and the mass resolving power only depends on the m/z resolution. Prior to this work, the best resolving power demonstrated experimentally for CD-MS was 700. Here we demonstrate a resolving power of >14,600, 20-times higher than the previous best. Trajectory simulations were used to optimize the geometry and electrostatic potentials of the ELIT. We found conditions where the energy dependence of the oscillation frequency becomes parabolic, and then operated with a nominal ion energy at the minimum of the parabola. The 14,600 resolving power was obtained with a beam collimator before the ELIT. With the collimator removed, the resolving power of the optimized ELIT is 7300, which is still an order of magnitude higher than the previous best. The resolving power was demonstrated by resolving the isotope distributions for peptides and proteins. High resolution CD-MS measurements were then used to resolve the glycans on a monoclonal antibody and applied to the analysis of hepatitis B virus capsids. The results indicate that procedures for adduct removal need to be improved for the full benefit of the higher resolving power to be realized for higher mass species. However, these results represent a key step toward using CD-MS to analyze very complex protein mixtures where charge states are not well resolved in the m/z spectrum because of congestion from numerous overlapping peaks.

Controlled interlayer exciton ionization in an electrostatic trap in atomically thin heterostructures

Atomically thin semiconductor heterostructures provide a two-dimensional (2D) device platform for creating high densities of cold, controllable excitons. Interlayer excitons (IEs), bound electrons and holes localized to separate 2D quantum well layers, have permanent out-of-plane dipole moments and long lifetimes, allowing their spatial distribution to be tuned on demand. Here, we employ electrostatic gates to trap IEs and control their density. By electrically modulating the IE Stark shift, electron-hole pair concentrations above 2 × 1012 cm−2 can be achieved. At this high IE density, we observe an exponentially increasing linewidth broadening indicative of an IE ionization transition, independent of the trap depth. This runaway threshold remains constant at low temperatures, but increases above 20 K, consistent with the quantum dissociation of a degenerate IE gas. Our demonstration of the IE ionization in a tunable electrostatic trap represents an important step towards the realization of dipolar exciton condensates in solid-state optoelectronic devices.

A novel nanofiltration membrane with a dual-charged layer to simultaneously remove anions and cations from acid mine drainage

A novel nanofiltration (NF) membrane with a positively and negatively dual-charged layer was finely designed in this study. The membrane was prepared by co-deposition of 4-tert-butylpyrocatechol (TBC) and polyethyleneimine (PEI) and electrostatic interaction to assemble positively and negatively charged functional layers on a substrate which is polyamide (PA)-based NF membrane. The NF membrane achieved excellent retention capacity through the combined effects of Donnan repulsion and electrostatic field trapping. The prepared membrane had a dense but thin surface layer with an average pore size of 0.84 nm, enabling an improved membrane flux of 8.66 L/(m2·h·bar) and high rejection to divalent inorganic salt ions (93.56 % Mg2+, 99.56 % SO42-). The membrane was used to treat acid mine drainage (AMD) and achieved an excellent retention capacity for ions in AMD (93.25 % Mg2+, 91.58 % Ca2+, 94.22 % Mn2+, 95.96 % SO42-), meeting industrial wastewater discharge standards. In addition, the NF membrane demonstrated good anti-fouling performance during the AMD treatment and significant potential for environmental remediation applications.

Exploring the Potential Lipid-Lowering and Weight-Reducing Mechanisms of FH06 Fermented Beverages Based on Non-Targeted Metabolomics and Network Pharmacology

Investigating the intricate pathways through which FH06 fermentation broth exerts lipid-lowering and weight-loss effects is pivotal for advancing our comprehension of metabolic regulation and therapeutic interventions. Ultrahigh-performance liquid chromatography quadrupole electrostatic field orbit trap mass spectrometry (UHPLC-QE-MS) detection and the ChEMBL database were used to determine the effective compounds in the FH06 fermentation broth and predict their targets. The TTD database and DisGeNET database were used to query obesity-related targets. The STRING database was used to construct protein interaction information. The Gene Ontology (GO) database and the Kyoto Encyclopedia of Genes and Genomes (KEGG) database were used to perform biological function annotation (GO) and KEGG pathway enrichment analyses of the targets. Results: A total of 85 effective compounds were screened from the fermentation broth of FH06; these compounds may act on TP53, PPARG, TNF, and other targets through 10 signaling pathways, such as the chemical carcinogenesis-receptor activation and lipid and atherosclerosis pathways, and exert pharmacological effects, such as hypoglycemic effects and weight loss. They also have anti-inflammatory, antioxidant, antitumor, and immunoregulatory effects. These findings reveal the active ingredients of FH06 fermentation broth and its multi-target and multi-channel characteristics in lipid lowering and weight loss. This study has positive implications for the clinical treatment of obesity using FH06, providing a theoretical and scientific basis for further developing of FH06-assisted lipid-lowering products.

Detection of recurrent fluorescence from anthracene using an electrostatic ion beam trap

The recurrent fluorescence of anthracene cations (C14H10+) was investigated using an electrostatic ion beam trap. The photon emission from the excited anthracene cations confined in the trap was observed in the order of milliseconds. The photon yields as a function of the wavelength in the range of 450–860 nm were measured by optical filters and a cooled photomultiplier, which revealed that the observed photon emission is attributed to the D2 → D0 transition of C14H10+. However, the time range of the photon emission is considerably longer than that of the spontaneous emission induced by the D2 → D0 transition (<1 μs). The number of photons emitted by the recurrent fluorescence of C14H10+ as a function of time was calculated using the previously reported theoretical decay rates of C14H10+ by recurrent fluorescence and thermal dissociation. The calculation results justified the time dependence of the measured number of photons over the extended time range. These results demonstrate that we successfully detected recurrent fluorescence photons emitted from excited anthracene cations.

Electrostatic vehicle exhaust particle sensor for the evaluation of the diesel particulate filter (DPF)

A real-time electrostatic particle sensor has been developed to measure the concentration of soot in diesel exhaust. Based on the Venturi effect, the self-priming sampling probe of the sensor was designed to generate a pressure difference to drive particles into the detection region of the electrostatic trap. A detection module was developed for real-time measurement of the nanoamp current generated by charged soot within the probe. The microcurrent was amplified by the signal processing system of the sensor. To guarantee the precision of particles, it was essential to test the performance. The sensor was able to measure currents from −100 nA to −30 nA with a relative error of −0.01%. In addition, experiments comparing the sensor with a commercial instrument have shown that they correlate well. Furthermore, the standard deviation of the sensor was 0.001049 during a 36 h long-term test, which is lower than a commercial instrument with better stability. The sensor was investigated to demonstrate the detection of diesel particulate filter (DPF) failure. The results showed that the consistency between the sensor and the regulatory measurement equipment was good. The data ratios of the sensors installed at the front and rear of the DPF differed by many fold, which indicated that the sensor was able to determine the status of the exhaust system.

Gate Electrodes Enable Tunable Nanofluidic Particle Traps.

The ability to control the location of nanoscale objects in liquids is essential for fundamental and applied research from nanofluidics to molecular biology. To overcome their random Brownian motion, the electrostatic fluid trap creates local minima in potential energy by shaping electrostatic interactions with a tailored wall topography. However, this strategy is inherently static; once fabricated, the potential wells cannot be modulated. Here, we propose and experimentally demonstrate that such a trap can be controlled through a buried gate electrode. We measure changes in the average escape times of nanoparticles from the traps to quantify the induced modulations of 0.7 kBT in potential energy and 50 mV in surface potential. Finally, we summarize the mechanism in a parameter-free predictive model, including surface chemistry and electrostatic fringing, that reproduces the experimental results. Our findings open a route toward real-time controllable nanoparticle traps.

Bushen Formula promotes the decrease of HBsAg levels in patients with CHB by regulating Tfh cells and B-cell subsets

Ethnopharmacological relevanceBushen Formula (BSF) is the effective traditional Chinese medicine (TCM) for chronic hepatitis B (CHB) according to our previous researches. However, the special effectiveness of BSF treating CHB patients in different stages and the immunoregulatory mechanisms remain to be explored. Aim of the studyTo compare the therapeutic effects of BSF in both treatment-naive patients and Peg-IFN-α-treated patients, and explore the potential mechanism of immunomodulation. Materials and methodsUltra-high performance liquid chromatography-quadrupole electrostatic field-orbital trap high resolution mass spectrometry and the TCMSP database were used to determine the main components of BSF. Two hundred and sixty-six patients were enrolled in the retrospective study, and they were divided into the treatment group (T-Group, BSF plus Peg-IFN-α) and the control group (C-Group, Peg-IFN-α monotherapy). Within each group, patients were further grouped into subgroups, namely T1/C1 groups (treatment-naive patients, T1 = 34, C1 = 94) and T2/C2 groups (Peg-IFN-α-treated patients, T2 = 56, C2 = 82). Serum HBV markers, serum HBV DNA levels, serum ALT/AST and TCM symptoms were obtained from the record. Bioinformatics analysis was employed to obtain the potential immunoregulatory mechanisms of BSF treating CHB patients. Among patients in T2 and C2 group, peripheral mononuclear cells from 36 patients were used to analyze the characteristics of peripheral follicular helper T (Tfh) cells and B-cell subtypes by flow cytometry. Preparation of BSF-containing serum in rats. In vitro, the co-culture system of CXCR5+ cells and HepG2.2.15 cells was built to investigate the immunoregulatory effects of BSF. ResultsA total of 14 main active compounds were detected in BSF, which were deemed critical for the treatment of CHB. Our findings indicated that the T2-Group exhibited the higher percentage of HBsAg decline ≥ 1-log10 IU/ml and rate of HBeAg seroclearance compared to the C2-Group (35.7% vs. 15.9%, P = 0.033; 33.9% vs. 11.0%, P = 0.002). Additionally, the T2-Group demonstrated the higher percentage of HBsAg decline ≥ 1-log10 IU/ml and rate of HBeAg seroclearance compared to the T1-Group (35.7% vs. 14.7%, P = 0.031; 33.9% vs. 2.9%, P = 0.000). The total effective rate based on TCM clinical syndrome in T1-Group and T2-Group were significantly greater than those in C1-Group and C2-Group (85.3% vs. 61.7%, P = 0.012; 89.1% vs. 63.4%, P = 0.000). Bioinformatics analysis indicated that the immunoregulatory mechanisms of BSF treating CHB patients were mainly linked to the growth and stimulation of B-cell, T-cell differentiation, and the signaling pathway of the B-cell receptor. Furthermore, the frequencies of Tfh cells and its IL-21 level, and the IL-21R expressed by B-cell were all increased after BSF treatment. Additionally, in the co-culture system of CXCR5+ cells and HepG2.2.15 cells, HBsAg and HBeAg levels were decreased after BSF-containing serum treatment，as well as the up-regulating of Tfh cell frequencies and down-regulating of B-cell frequencies. ConclusionsBSF have the higher percentage of HBsAg decline and HBeAg seroclearance in Peg-IFN-α-treated patients compared with treatment-naive patients. The potential immunoregulatory mechanism may correlate with promoting the interaction between Tfh cells and B-cell through IL-21/IL-21R signaling pathway.

Electrostatic Trapping of N_{2} Molecules in High Rydberg States.

N_{2} molecules traveling in pulsed supersonic beams have been excited from their X ^{1}Σ_{g}^{+} ground electronic state to long-lived Rydberg states with principal quantum numbers between 39 and 48 using a resonance-enhanced two-color three-photon excitation scheme. The Rydberg states populated had static electric dipole moments exceeding 5000 D which allowed deceleration of the molecules to rest in the laboratory-fixed frame of reference and three-dimensional trapping using inhomogeneous electric fields. The trapped molecules were confined for up to 10ms, with effective trap decay time constants increasing with principal quantum number, and ranging from 450 to 700 μs. These observations, and comparison with the results of similar measurements with He atoms, indicate that the decay dynamics of the trapped Rydberg N_{2} molecules are dominated by spontaneous emission and do not exhibit significant contributions from effects of intramolecular interactions that lead to non-radiative decay.

Molecular sieve 13X activated zeolite for CO2 filter in air purifier

Indoor air quality is crucial for health. Room with high CO2 concentration can cause sick building syndrome such as dizziness, nausea, fatigue, and breathing difficulties. In addition to the air circulation, air filtering can reduce CO2 and improve the indoor air quality. The integration of activated zeolite into conventional air cleaning filters, which lack specific CO2 gas selectivity, presents a promising solution for CO2 reduction. Possessing cage-like porous structures and extra framework cations, activated zeolites have been known as gas adsorbers via physisorption and chemisorption mechanism. Activated zeolites have been reported to have high selectivity to CO2 gas via electrostatic interaction and trapping in small pores. In this study, we integrated the molecular sieve13X activated zeolite (MSAZ) with typical pore size around 1 nm to the conventional filters in air purifier which does not have specific selectivity to CO2 gas. By varying the MSAZ masses, we demonstrated that the MSAZ addition effectively reduce around 147 up to 316 ppm CO2 depending on the MSAZ mass and the air purifier fan speed. This value is extremely higher compared to 4 ppm CO2 reduction by commercial carbon filter without MSAZ. Larger mass and faster fan speed resulted in higher CO2 reduction. This study proves the prospective application of the MSAZ for CO2 reduction, to improve the indoor air quality and to avoid adverse effects of CO2 exposure.

Tandem mass spectrometry using continuous-wave infrared multiphoton dissociation in an electrostatic linear ion trap.

The electrostatic linear ion trap (ELIT) can be operated as a multi-reflection time-of-flight (MR-TOF) or Fourier transform (FT) mass analyzer. It has been shown to be capable of performing high-resolution mass analysis and high-resolution ion isolations. Although it has been used in charge-detection mass spectrometry (CDMS), it has not been widely used as a conventional mass spectrometer for ensemble measurements of ions, or for tandem mass spectrometer. The advantages of tandem mass spectrometer with high-resolution ion isolations in the ELIT have thus not been fully exploited. A homebuilt ELIT was modified with BaF2 viewports to facilitate transmission of a laser beam at the turnaround point of the second ion mirror in the ELIT. Fragmentation that occurs at the turnaround point of these ion mirrors should result in minimal energy partitioning due to the low kinetic energy of ions at these points. The laser was allowed to irradiate ions for a period of many oscillations in the ELIT. Due to the low energy absorption of gas-phase ions during each oscillation in the ELIT, fragmentation was found to occur over a range of oscillations in the ELIT generating a homogeneous ion beam. A mirror-switching pulse is shown to create time-varying perturbations in this beam that oscillate at the fragment ion characteristic frequencies and generate a time-domain signal. This was found to recover FT signal for protonated pYGGFL and pSGGFL precursor ions. Fragmentation at the turnaround point of an ELIT by continuous-wave infrared multiphoton dissociation (cw-IRMPD) is demonstrated. In cases where laser power absorption is low and fragmentation occurs over many laps, a mirror-switching pulse may be used to recover varying time-domain signal. The combination of laser activation at the turnaround points and mirror-switching isolation allows for tandem MS in the ELIT.

The Potential Transcriptomic and Metabolomic Mechanisms of ATO and ATRA in Treatment of FLT3-ITD Acute Myeloid Leukemia.

Acute myeloid leukemia (AML) with Fms-like tyrosine kinase 3 gene internal tandem duplication (FLT3-ITD) mutations has a poor prognosis. The combination of arsenic trioxide (ATO) and all-trans retinoic acid (ATRA) has a synergistic killing effect on leukemia cells with FLT3-ITD mutation. However, the mechanism, especially the changes of gene expression and metabolic activity remain unclear. Here we explore the transcriptome and metabolomics changes of FLT3-ITD AML cells treated with ATO/ATRA. RNA-seq was used to identify differential expressed genes (DEGs), and ultra-high performance liquid chromatography-quadrupole electrostatic field orbital trap mass spectrometry (UHPLC-QE-MS) nontargeted metabolomics method was used to screen out the differential metabolites in FLT3-ITD mutant cell lines treated with ATRA and ATO. KEGG pathway database was utilized for pathway exploration and Seahorse XF24 was used to detect extracellular acidification rate (ECAR). Metabolic polymerase chain reaction (PCR) array and real-time quantitative PCR (RT-qPCR) were used to detect mRNA levels of key metabolic genes of glycolysis and fatty acid after drug treatment. A total of 3873 DEGs were identified and enriched in 281 Gene Ontology (GO) terms, among which 210 were related to biological processes, 43 were related to cellular components, and 28 were related to molecular functions. Besides, 1794 and 927 differential metabolites were screened in positive and negative ion mode separately, and 59 different metabolic pathways were involved, including alanine-aspartate-glutamate metabolic pathway, arginine, and proline metabolic pathway, glycerophospholipid metabolic pathways, etc. According to KEGG Pathway analysis of transcriptome combined with metabolome, glycolysis/gluconeogenesis pathway and fatty acid metabolism pathway were significantly founded enriched. ATRA + ATO may inhibit the glycolysis of FLT3-ITD AML cells by inhibiting FLT3 and its downstream AKT/HK2-VDAC1 signaling pathway. The gene transcription profile and metabolites of FLT3-ITD mutant cells changes significantly after treatment, which might be related to the anti-FLT3-ITD AML effect. The screened DEGs, differential metabolites pathway are helpful in studying the mechanism of anti-leukemia effects and drug targets.

Ion-Ion Interaction Induced Nondispersive Dynamics in an Electrostatic Ion Beam Trap

Ion-Ion Interaction Induced Nondispersive Dynamics in an Electrostatic Ion Beam Trap

Surface-induced dissociation of protein complex ions in a modified electrostatic linear ion trap

The electrostatic linear ion trap (ELIT) is a device that can provide mass analysis via frequency measurement, followed by Fourier transformation from the frequency domain to the time domain, or via time measurement in a multi-reflection time-of-flight measurement. ELIT devices have been demonstrated to be capable of relatively high mass measurement resolution as well as high-resolution ion isolation capabilities. We have been exploring the possibility of developing the ELIT geometry as a stand-alone high-performance tandem mass spectrometer for native mass spectrometry (MS) studies. In this context, it is desirable to use an activation method capable of dissociating the high-mass complexes encountered in native MS. To this end, we describe the implementation of surface-induced dissociation (SID) in an ELIT and describe initial results for protein complexes generated under native conditions in which ion isolation, fragmentation, and product ion mass analysis all occur within the ELIT.

Edge-Confined Excitons in Monolayer Black Phosphorus.

Quantum confinement of two-dimensional excitons in van der Waals materials via electrostatic trapping, lithographic patterning, Moiré potentials, and chemical implantation has enabled significant advances in tailoring light emission from nanostructures. While such approaches rely on complex preparation of materials, natural edges are a ubiquitous feature in layered materials and provide a different approach for investigating quantum-confined excitons. Here, we observe that certain edge sites of monolayer black phosphorus (BP) strongly localize the intrinsic quasi-one-dimensional excitons, yielding sharp spectral lines in photoluminescence, with nearly an order of magnitude line width reduction. Through structural characterization of BP edges using transmission electron microscopy and first-principles GW plus Bethe-Salpeter equation (GW-BSE) calculations of exemplary BP nanoribbons, we find that certain atomic reconstructions can strongly quantum-confine excitons resulting in distinct emission features, mediated by local strain and screening. We observe linearly polarized luminescence emission from edge reconstructions that preserve the mirror symmetry of the parent BP lattice, in agreement with calculations. Furthermore, we demonstrate efficient electrical switching of localized edge excitonic luminescence, whose sites act as excitonic transistors for emission. Localized emission from BP edges motivates exploration of nanoribbons and quantum dots as hosts for tunable narrowband light generation, with future potential to create atomic-like structures for quantum information processing applications as well as exploration of exotic phases that may reside in atomic edge structures.

Study on removal of oxytetracycline by KOH-modified chestnut shell biochar: Based on two-dimensional spectroscopy and molecular density functional theory

The adsorption type and mode of biochar have been extensive research. However, as an indispensable link to reveal the adsorption mechanism, the study of the adsorption sequence is greatly lacking, especially for different pollutants, the way of adsorption is different. In this study, the observation of the adsorption sequence was amplified by KOH modification and optimization of experimental conditions. Persistent radicals (PFRs) combined with liquid mass spectrometry (LC-MS) eliminated interference from oxidation-reduction. Notability, two-dimensional correlation spectroscopy (2D-COS), Raman and Fourier-transform infrared (FTIR) spectroscopy reveals that the vibration amplitude and velocity of the hydroxyl group are better than those of the carboxyl group, methyl group, and methylene group under time interference. Electrostatic adsorption (EA), H-bood (HB), and π-π* contribute 63.5 %, 35.3 %, and 1.2 %, respectively, to the adsorption of oxytetracycline (OTC). The density functional calculation shows that the nucleophilic and electrophilic reactions of OTC are easy to occur near oxygen atoms and nitrogen atoms. The Fukui function proves that the free radical weight of the N atom is 0.096, which is further confirmed the theoretical predictions by liquid chromatography and four-stage electrostatic field orbital trap mass spectrometry. Finally, this study provides a deeper insight into the biochar adsorption OTC.

Multi-residue determination of five quinoxalines and three their metabolites in poultry feathers and its application for depletions of olaquindox and quincetone in chickens

A method for the simultaneous determination of eight quinoxalines and their metabolites in poultry feathers was developed in this study using ultra-performance liquid chromatography combine with quadrupole linear ion trap electrostatic field orbit trap high resolution mass spectrometer. Specificity, matrix effect, linearity, trueness, repeatability, reproducibility, and stability using the Commission of the European Communities, Regulation (EU) 2021/808. The correlation coefficients were all greater than 0.99. The average recoveries of the eight compounds ranged from 76.1% to 112.8%, with coefficient of variation of less than 15%. The limits of detection and quantification of the method were 0.04–0.1 μg/kg and 0.12–0.3 μg/kg, respectively. The method has been successfully applied to depletions of olaquindox and quincetone in feathers of laying hens. Methylquinoxaline-2-carboxylic acid and quincetone are the main metabolites in olaquindox and quincetone in feather, respectively.

Electrostatic Linear Ion Trap Optimization Strategy for High Resolution Charge Detection Mass Spectrometry.

Single ion mass measurements allow mass distributions to be recorded for heterogeneous samples that cannot be analyzed by conventional mass spectrometry. In charge detection mass spectrometry (CD-MS), ions are detected using a conducting cylinder coupled to a charge sensitive amplifier. For optimum performance, the detection cylinder is embedded in an electrostatic linear ion trap (ELIT) where trapped ions oscillate between end-caps that act as opposing ion mirrors. The oscillating ions generate a periodic signal that is analyzed by fast Fourier transforms. The frequency yields the m/z, and the magnitude provides the charge. With a charge precision of 0.2 elementary charges, ions can be assigned to their correct charge states with a low error rate, and the m/z resolving power determines the mass resolving power. Previously, the best mass resolving power achieved with CD-MS was 300. We have recently increased the mass resolving power to 700, through the better optimization of the end-cap potentials. To make a more dramatic improvement in the m/z resolving power, it is necessary to find an ELIT geometry and end-cap potentials that can simultaneously make the ion oscillation frequency independent of both the ion energy and ion trajectory (angular divergence and radial offset) of the entering ion. We describe an optimization strategy that allows these conditions to be met while also adjusting the signal duty cycle to 50% to maximize the signal-to-noise ratio for the charge measurement. The optimized ELIT provides an m/z resolving power of over 300 000 in simulations. Coupled with the high precision charge determination available with CD-MS, this will yield a mass resolving power of 300 000. Such a high mass resolving power will be transformative for the analysis of heterogeneous samples.