Search

Intercalation in two-dimensional (2D) materials can modify their physical, chemical, and electronic properties. This modification enables the tailoring of 2D material characteristics, enhancing their performance and expanding their applications in various fields. The friction performance of 2D materials such as MoS 2 and graphite has a strong dependence on their interlayer spacing, and they exhibit an increase in d -spacing associated with a reduction in friction performance. The ability to control the interlayer spacing of Ti 3 C 2 T z MXene has proven beneficial for energy storage applications such as batteries and supercapacitors, but no one has utilized this control of interlayer spacing for lubrication. In this study, we demonstrate that interlayer spacing of multilayer (ML) Ti 3 C 2 T z MXene can be controlled through chemical intercalation and its direct effects on the electrical conductivity and friction performance. We observed a notable decrease in electrical conductivity in vacuum-filtered ML-Ti 3 C 2 T z MXene films, which was attributed to an increased internal resistance resulting from the expansion of the interlayer gap. We also found a significant reduction in the coefficient of friction for ML-Ti 3 C 2 T z MXene with an increased d -spacing. This reduction is attributed to a weakened attraction of individual ML-Ti 3 C 2 T z MXene layers (intercalated). Under a tangential force, it becomes easier to slide within the larger interlayer gap with weakened van der Waals forces. This work provides insights into the tunability of MXene properties through interlayer spacing, offering potential applications requiring materials with specific electrical and friction characteristics.

Graphene oxide (GO) was prepared from the graphite electrode of waste dry cells, and the application of the prepared GO as a potential adsorbent for rapid and effective removal of an antibiotic, azithromycin (AZM), has been investigated. The synthesis process of GO is very simple, cost-effective, and eco-friendly. As-prepared GO is characterized by field-emission scanning electron microscopy, energy-dispersive X-ray, transmission electron microscopy, X-ray diffractometry, Fourier transform infrared spectroscopy, elemental analysis, Brunauer-Emmett-Teller sorptometry, and zeta potential analysis. The obtained GO has been employed for removal of the widely used AZM antibiotic from an aqueous solution. The quantitative analysis of AZM before and after adsorption has been carried out by liquid chromatography tandem mass spectrometry. The adsorption of AZM by GO was performed in a batch of experiments where the effects of adsorbent (GO) dose, solution pH, temperature, and contact time were investigated. Under optimum conditions (pH = 7.0, contact time = 15 min, and adsorbent dose = 0.25 g/L), 98.8% AZM was removed from the aqueous solution. The rapid and effective removal of AZM was significantly controlled by the electrostatic attractions and hydrogen bonding on the surface of GO. Adsorption isotherms of AZM onto GO were fitted well with the Freundlich isotherm model, while the kinetic data were fitted perfectly with the pseudo-second order. Therefore, the simple, cost-effective, and eco-friendly synthesis of GO from waste material could be applicable to fabricate an effective and promising low-cost adsorbent for removal of AZM from aqueous media., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

Harnessing electrochemical energy in an engineered electrical circuit from biochemical substrates in the human body using biofuel cells is gaining increasing research attention in the current decade due to the wide range of biomedical possibilities it creates for electronic devices. In this report, we describe and characterize the construction of just such an enzymatic biofuel cell (EBFC). It is simple, mediator-free, and glucose-powered, employing only biocompatible materials. A novel feature is the two-dimensional mesoporous thermally reduced graphene oxide (rGO) host electrode. An additionally novelty is that we explored the potential of using biocompatible, low-cost filter paper (FP) instead of carbon paper, a conductive polymer, or gold as support for the host electrode. Using glucose (C 6 H 12 O 6 ) and molecular oxygen (O 2 ) as the power-generating fuel, the cell consists of a pair of bioelectrodes incorporating immobilized enzymes, the bioanode modified by rGO-glucose oxidase (GOx/rGO), and the biocathode modified by rGO-laccase (Lac/rGO). Scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDX), transmission electron microscopy, and Raman spectroscopy techniques have been employed to investigate the surface morphology, defects, and chemical structure of rGO, GOx/rGO, and Lac/rGO. N 2 sorption, SEM/EDX, and powder X-ray diffraction revealed a high Brunauer-Emmett-Teller surface area (179 m 2 g -1 ) mesoporous rGO structure with the high C/O ratio of 80:1 as well. Results from the Fourier transform infrared spectroscopy, UV-visible spectroscopy, and electrochemical impedance spectroscopy studies indicated that GOx remained in its native biochemical functional form upon being embedded onto the rGO matrix. Cyclic voltammetry studies showed that the presence of mesoporous rGO greatly enhanced the direct electrochemistry and electrocatalytic properties of the GOx/rGO and Lac/rGO nanocomposites. The electron transfer rate constant between GOx and rGO was estimated to be 2.14 s -1 . The fabricated EBFC (GOx/rGO/FP-Lac/rGO/FP) using a single GOx/rGO/FP bioanode and a single Lac/rGO/FP biocathode provides a maximum power density ( P max ) of 4.0 nW cm -2 with an open-circuit voltage ( V OC ) of 0.04 V and remains stable for more than 15 days with a power output of ∼9.0 nW cm -2 at a pH of 7.4 under ambient conditions.

Diarrheal illnesses from enteric pathogens are a leading cause of death in children under five in low- and middle-income countries (LMICs). Sanitation is one way to reduce the spread of enteric pathogens in the environment; however, few studies have investigated the effectiveness of sanitation in rural LMICs in reducing pathogens in the environment. In this study, we measured the impact of a sanitation intervention (dual-pit latrines, sani-scoops, child potties delivered as part of a randomized control trial, WASH Benefits) in rural Bangladeshi household compounds by assessing prevalence ratios, differences, and changes in the concentration of pathogen genes and host-specific fecal markers. We found no difference in the prevalence of pathogenic Escherichia coli , norovirus, or Giardia genes in the domestic environment in the sanitation and control arms. The prevalence of the human fecal marker was lower on child hands and the concentration of animal fecal marker was lower on mother hands in the sanitation arm in adjusted models, but these associations were not significant after correcting for multiple comparisons. In the subset of households with ≥10 individuals per compound, the prevalence of enterotoxigenic E. coli genes on child hands was lower in the sanitation arm. Incomplete removal of child and animal feces or the compound (versus community-wide) scale of intervention could explain the limited impacts of improved sanitation.

We propose to use cRFP (common Repository of FBS Proteins) in the MS (mass spectrometry) raw data search of cell secretomes. cRFP is a small supplementary sequence list of highly abundant fetal bovine serum proteins added to the reference database in use. The aim behind using cRFP is to prevent the contaminant FBS proteins from being misidentified as other proteins in the reference database, just as we would use cRAP (common Repository of Adventitious Proteins) to prevent contaminant proteins present either by accident or through unavoidable contacts from being misidentified as other proteins. We expect it to be widely used in experiments where the proteins are obtained from serum-free media after thorough washing of the cells, or from a complex media such as SILAC, or from extracellular vesicles directly.

Fecal indicator organisms are measured to indicate the presence of fecal pollution, yet the association between indicators and pathogens varies by context. The goal of this study was to empirically evaluate the relationships between indicator Escherichia coli , microbial source tracking markers, select enteric pathogen genes, and potential sources of enteric pathogens in 600 rural Bangladeshi households. We measured indicators and pathogen genes in stored drinking water, soil, and on mother and child hands. Additionally, survey and observational data on sanitation and domestic hygiene practices were collected. Log 10 concentrations of indicator E. coli were positively associated with the prevalence of pathogenic E. coli genes in all sample types. Given the current need to rely on indicators to assess fecal contamination in the field, it is significant that in this study context indicator E. coli concentrations, measured by IDEXX Colilert-18, provided quantitative information on the presence of pathogenic E. coli in different sample types. There were no significant associations between the human fecal marker (HumM2) and human-specific pathogens in any environmental sample type. There was an increase in the prevalence of Giardia lamblia genes, any E. coli virulence gene, and the specific E. coli virulence genes stx1/2 with every log 10 increase in the concentration of the animal fecal marker (BacCow) on mothers' hands. Thus, domestic animals were important contributors to enteric pathogens in these households.

Water, sanitation, and hygiene interventions have varying effectiveness in reducing fecal contamination in the domestic environment; delivering them in combination could yield synergies. We conducted environmental assessments within a randomized controlled trial in Bangladesh that implemented single and combined water treatment, sanitation, handwashing (WSH) and nutrition interventions (WASH Benefits, NCT01590095). After one and two years of intervention, we quantified fecal indicator bacteria in samples of drinking water (from source or storage), child hands, children's food and sentinel objects. In households receiving single water treatment interventions, Escherichia coli prevalence in stored drinking water was reduced by 50% and concentration by 1-log. E. coli prevalence in food was reduced by 30% and concentration by 0.5-log in households receiving single water treatment and handwashing interventions. Combined WSH did not reduce fecal contamination more effectively than its components. Interventions did not reduce E. coli in groundwater, on child hands and on objects. These findings suggest that WSH improvements reduced contamination along the direct transmission pathways of stored water and food but not along indirect upstream pathways. Our findings support implementing water treatment and handwashing to reduce fecal exposure through water and food but provide no evidence that combining interventions further reduces exposure.

Energy transfer rate constants for Ne(2p(5)3p) and Kr(4p(5)5p) atoms colliding with ground state rare gas atoms (Rg) have been measured. In part, this study is motivated by the possibility of using excited rare gas atoms as the active species in optically pumped laser systems. Rg(np(5)(n + 1)s) metastable states may be produced using low-power electrical discharges. The potential then exits for optical pumping and laser action on the np(5)(n + 1)p ↔ np(5)(n + 1)s transitions. Knowledge of the rate constants for collisional energy transfer and deactivation of the np(5)(n + 1)p states is required to evaluate the laser potential for various Rg + buffer gas combinations. In the present study we have characterized energy transfer processes for Ne (2p(5)3p) + He for the six lowest energy states of the multiplet. Rate constants for state-to-state transfer have been determined. Deactivation of the lowest energy level of Kr (4p(5)5p) by He, Ne, and Kr has also been characterized. Initial results suggest that Kr (4p(5)5p) + Ne mixtures may be the best suited for optically pumped laser applications., (© 2011 American Chemical Society)

Rotational relaxation rates for HBr(v = 1) colliding with helium atoms at room temperature have been measured using a time-resolved optical-optical double resonance technique. Rotational state selective excitation of v = 1 for rotational levels in the range J = 1-9 was achieved by stimulated Raman pumping. The population decay in the prepared states and the transfer of population to nearby rotational states was monitored via 2 + 1 resonance-enhanced multiphoton ionization (REMPI) spectroscopy using the g(3)Σ(-)-X(1)Σ(+) (0-1) band. Collision-induced population evolution for transfer events with |ΔJ| ≤ 8 was observed at pressures near 0.7 Torr. The experimental data were analyzed using fitting and scaling functions to generate state-to-state rotational energy transfer rate constant matrices. Total depopulation rate constants were found to be in the range (1.3 to 2.0) × 10(-10) cm(3) s(-1). As a test of current computational methods, state-to-state rotational energy transfer rate constants were calculated using ab initio theory. The total removal rate constants were in good agreement with the measured values, but the transfer probabilities for events with |ΔJ| ≥ 3 were underestimated. Inspection of the anisotropic characteristics of the potential energy surface did not yield an obvious explanation for the discrepancies, but it is most likely that the problem stems from inaccuracies in the potential surface.

Quenching of excited iodine atoms (I(5p5, 2P1/2)) by nitrogen oxides are processes of relevance to discharge-driven oxygen iodine lasers. Rate constants at ambient and elevated temperatures (293-380 K) for quenching of I(2P1/2) atoms by NO2, N2O4, and N2O have been measured using time-resolved I(2P1/2) --> I(2P3/2) 1315 nm emission. The excited atoms were generated by pulsed laser photodissociation of CF3I at 248 nm. The rate constants for I(2P1/2) quenching by NO2 and N2O were found to be independent of temperature over the range examined with average values of (2.9 +/- 0.3) x 10(-15) and (1.4 +/- 0.1) x 10(-15) cm3 s(-1), respectively. The rate constant for quenching of I(2P1/2) by N2O4 was found to be (3.5 +/- 0.5) x 10(-13) cm3 s(-1) at ambient temperature.

The recent demonstration of a discharge-driven oxygen-iodine laser has generated renewed interest in the kinetics of iodine interacting with electronically excited O2 and atomic O. Kinetic measurements that are of relevance to the laser have been carried out using 193 nm pulsed laser photolysis of N2O/I2/CO2 mixtures. Singlet oxygen was generated in this system by the reaction O(1D)+N2O-->O2(a1Deltag, X3Sigma-g)+N2. The fraction of electronically excited O2 produced by this channel was shown to be >0.9. The secondary photochemistry of the N2O/I2/CO2 system was characterized by monitoring the time histories of I(2P1/2), I2, IO, and O2(a). Kinetic modeling of these data was used to determine the rate constant for the deactivation of I(2P1/2) by O(3P) (k=(1.2+/-0.1)x10(-11) cm3 s(-1)). Quenching of I(2P1/2) by O(3P) is suppressed in the discharge-driven laser by using NO2 to scavenge the O atoms. The reaction O(3P)+NO2-->O2+NO is sufficiently exothermic for the production of O2(a), and it has been speculated that this channel may be significant in the laser excitation kinetics. Photolysis of NO2 was used to probe this reaction. O2(a) was not detected, and an upper bound of <0.1 for its production in the reaction of O(3P) or O(1D) with NO2 was established.