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We investigated the effect that two common types of cationic polyelectrolytes used in papermaking might have on the performance of paper diagnostics using blood typing as an example. The results were analyzed in terms of red blood cells (RBC) retention and antibody-antigen specificity. Two questions were addressed: (1) can poly(amido-amine) epichlorohydrin (PAE) typically used for paper wet strength affect the diagnostic performance? (2) can high molecular weight cationic polyacrylamide (CPAM) employed as retention aid enhance or affect the selectivity and sensitivity of paper diagnostics? A series of paper varying in type of fibers and drying process were constructed with PAE and tested for blood typing performance. Residual PAE has no significant effect on blood typing paper diagnostics under normal conditions. Positives are unaffected with PAE, while negatives lose slight sharpness as some RBCs are unselectively retained. CPAM, the most common retention aid, can also be used to retain cells and biomolecules on paper. Paper towel was treated with CPAM solutions varying in polymer concentration and charge density and tested for blood typing. We found that CPAM dried on paper can retain RBC. CPAM affects the negative tests by retaining non-specifically individual RBC on fibers. RBC retention increases non-linearly with the CPAM charge density and concentration. As expected, wet CPAM retain RBCs at concentrations higher than 0.1wt%. As paper diagnostics are becoming a reality, more realistic papers than the Whatman filter paper will be engineered. This study provides guidance on how best use the required polymeric wet-strength and retention agents., (Crown Copyright © 2015. Published by Elsevier B.V. All rights reserved.)

Diffuse reflectance spectroscopy can be successfully used for the quantitative determination of small amounts of pollutants like metals. The remission function was found to be linearly proportional to the concentration, when we applied the Kubelka-Munk equation. The color reactions of Cu(II), Co(II), and Ni(II) with dithiooxamide, were realised on filter paper. Reaction between Fe(III) and ammonium thiocyanate was realized on filter paper and gelatine matrix. All measurements were accomplished with a laboratory-constructed reflectometer. We have obtained a calibration curve by plotting the optical density of reflectance A(R) vs log of the mol l(-1) concentration. Limits of detection at the 10(-4) M level were estimated for all the compounds. Linear dynamic range extend over one order of magnitude and shows the potential of device for the quantitative analysis of environmental pollutants.

Cationized birch xylan was prepared and its use as a papermaking chemical was evaluated. The focus was on studying the effects of cationized birch xylan on the wet and dry strength of fine paper. The results of the laboratory experiments show that the addition of 3 percent of cationized birch xylan to birch kraft pulp improved the initial wet strength of the web by 30 percent compared to base stock at a solids content of 55%. Furthermore, the tensile stiffness of the wet web increased by approximately a third and the dry tensile strength improved by 26%, while the dry elastic modulus was not changed. The improvements in the strength properties were clear when compared to the base stock, but not as high as achieved with conventionally used cationized starch. The difference between the xylan and starch is most likely due to the shorter polymer chain length of the cationized xylan. [ABSTRACT FROM AUTHOR]

Highlights: [•] Improvement of the direct quantification with analytical pyrolysis. [•] Optimization of the chromatographic parameters after pyrolysis of cationic starch. [•] Quantification of cationic starches in cellulose matrixes. [•] Validation of the cationic starch quantification in paper samples. [ABSTRACT FROM AUTHOR]

[Display omitted] • GQD-DDT and GQD-MPA was synthesized using novel hydrothermal protocol. • GQD-DDT and GQD-MPA was used for the identification of cations using colorimetric and spectrophotometric assay. • GQD-DDT and GQD-MPA have well activity for ion sensing in aqueous solution. This study describes the synthesis of various types of thiolated-graphene quantum dots (GQDs) for the simultaneous multi-sensing of heavy metal ions using one-droplet microfluidic paper-based analytical devices (OD- µ PADs). For the first time, functionalized GQDs were synthesized and stabilized on the surface of hydrophobic fiber-glass with simple manufacturing and assembly strategy towards colorimetric chemosensing of ions including iron, copper, cobalt, mercury, chrome, manganese, and nickel. For this purpose, GQDs are functionalized by various organic species including cysteamine, decanethiol, and mercaptopropionic acid (MPA) towards specific electrostatic interaction with metal ions of Fe (II), Cu (II), Co(II), Hg (II), Mn (II), and Ni (II). Therefore, an innovative GQDs-based miniaturized chemo-system was proposed for the environmental analysis. Additionally, the results were confirmed using fluorescence spectrometry as an optical detection method. Finally, this simple and efficient colorimetric platform was used for facile metal ions detection in human urine models, and environmental fluids, which can provide a commercial device for sensing contaminants by non-professional users in biomedical/environmental mixture. As an economical technique, this platform presents a "mix-and-sense" system without dye (as a side substance) or chemical treatments. The low instrumental requirements, the color uniformity, and the disposability of OD- μ PADs approve the commercial application of the engineered ion-chemosensor. [ABSTRACT FROM AUTHOR]

A new approach for the chemical modification of the surface of paper based on the application of colloidal mixtures containing cationic starch and polyoxometalates on uncoated base paper is presented. Polyoxometalates with the Keggin-type structure and physical properties similar to those presented by coating pigments, namely H3PW12O40∙23H2O, H4SiW12O40∙24H2O, and K7PW11O39∙9H2O, have been used in order to improve the quality of inkjet printing. The analysis of the different samples by FTIRATR spectroscopy showed the presence of the polyoxometalates (and the cationic starch) on the top surface of the paper. In addition, the determination of surface energy parameters, namely the polar component (σsp) and the dispersive component (σsd) of the surface energy, by contact angle measurements revealed that, for the new samples, the polar component level was much higher than that of the uncoated base paper. The quality of inkjet printing, evaluated by parameters such as the gamut area and the optical density, was considerably improved by these surface treatments. [ABSTRACT FROM AUTHOR]

Accumulation of interfacial space charge in oil-paper interface is a critical issue in insulation diagnostics of transformers. This interfacial charge mainly accumulates due to the conductivity difference of oil and paper. Accumulation of interfacial charge leads to localized field enhancement, which further leads to partial discharges and acceleration in the aging of insulation. Therefore, from the point of view of transformer insulation diagnostics, assessment of interfacial charge is very important. However, it is not easy to estimate interfacial space charge behavior from the transformer diagnostics methods currently in use. In case of Polarization-Depolarization Current (PDC) measurement, a well known method for transformer condition monitoring, the effect of interfacial charge is reflected in the non-linearity of current response during polarization and de-polarization. During de-polarization process, a part of the interfacial charge accumulated during polarization period is absorbed by the electrodes producing a current, which is difficult to separate using conventional linear dielectric theory. In this paper, an attempt has been made to separate this current component from de-polarization current through considering charge de-trapping mechanism. Terming this current component as de-trapping current, its relationship with other parameters of transformer insulation is discussed. The developed methodology has been applied on several practical transformers. It was observed that the time constant of de-trapping current is related to the paper conductivity, oil conductivity, dissipation factor and age of the insulation. [ABSTRACT FROM PUBLISHER]

Abstract: This study examines and quantifies the effect of cationic polyacrylamide (CPAM) dissolution kinetics and charge density on the adsorption and aggregation state of gold nanoparticles (AuNPs) on paper and the resulting Surface Enhanced Raman Scattering (SERS) performance. Dissolution kinetics of CPAM of different charge density was studied by monitoring their viscosity and hydrodynamic diameter over regular intervals of time. It was found that the degree of dissolution of CPAM greatly affected the surface coverage and aggregation of AuNPs on the CPAM pre-adsorbed paper substrate and their SERS reproducibility. CPAM of higher charge density dissolves faster and produced a more uniform aggregation and higher surface coverage of AuNPs on paper for a higher and more reproducible Raman EF. Understanding the CPAM dissolution process enables the optimization of SERS performance of the AuNPs-paper as a bio-diagnostic platform. [Copyright &y& Elsevier]

Abstract: This study examines and quantifies the effect of cationic polyelectrolyte adsorption on paper on the aggregation and retention of gold nanoparticles (AuNPs) to optimize their Surface Enhanced Raman Scattering (SERS) enhancement factor and sensitivity. Aggregation of metallic nanoparticles is known as a key factor for intense SERS enhancement. Paper substrates were treated with aqueous solutions of cationic polyacrylamide (CPAM) varying in concentration, charge density, and molecular weight to control the AuNPs’ aggregate size distribution and surface coverage on paper. The Raman Enhancement Factor of AuNPs-CPAM paper was almost an order of magnitude greater than for the untreated AuNPs paper. The high loading and uniform distribution of AuNPs aggregates on CPAM pre-treated paper contributed toward the excellent SERS reproducibility, sensitivity, and high enhancement factor. This configuration of AuNP on paper was favoured by treating the substrate with CPAM solutions of higher concentrations, higher charge density, and greater molecular weight. [Copyright &y& Elsevier]

1-octadecanol is known to be a highly effective agglomerating agent for laser toner ink. However, the office waste paper used in the actual production often contains various types of inks. The effect of the offset ink and types of surfactants with different charge characteristics were studied relative to the agglomeration of the laser toner ink under neutral pulping conditions. It was found that the addition of a small amount of the offset ink printed waste paper was beneficial for the agglomeration of the laser toner ink. The optimal percentage of addition is 12.5% to 25%. The offset printed ink had a positive charge of 0.001±0.0005 mEq/g when the offset ink was treated by 70°C water at neutral conditions. Addition of a proper amount of cationic surfactant was beneficial to improve the agglomeration at any ratio of the mixed laser printed and offset waste papers. When the percentage of offset waste paper was less than 50%, the addition of anionic surfactant and nonionic surfactant was harmful for agglomeration, and there was no significant effect at higher offset content. [ABSTRACT FROM AUTHOR]

Abstract: Large numbers of soil samples are routinely analyzed using methylene blue (MB) titration to determine clay content. Although, the MB filter paper spot test titration is simple, it is labor-intensive, subjective, and leaves no record for subsequent re-examination. Preliminary thermometric monitoring of the titration indicated a switch from endothermic to exothermic reaction during titration. We examined this nearly universal property of physicochemical processes as a potential replacement method to automate the MB clay titration, making use of literature data. We translated the isothermal enthalipmetric titration of montmorillonite using MB by Rytwo and Ruiz-Hitzky to an adiabatic thermometric titration (2003). The plot of temperature versus titrant volume gave two intersecting linear segments dependent on the titrated percentage of the clay''s cation exchange capacity (CEC). The MB filter paper spot test endpoint reflects the first excess MB that persists in the solid suspension, which also happens to be a function of the clay''s CEC. The spot test endpoint is correlated to the thermometric indicator point and, for montmorillonite, the two are related by an exact factor of two. Although this factor will naturally be dependent on the clay minerals in the samples, the analyses show that the thermometric indicator titration method is a viable replacement for the spot test. The proposed automation is commonplace as it is practiced with other types of titrations. [Copyright &y& Elsevier]

Novel polyepinephrine-modified NaYF 4 :Yb,Tm upconversion luminescent nanoparticles (UCNP@PEP) were prepared via the self-polymerization of epinephrine on the surfaces of the UCNPs for selective sensing of Fe 3+ inside a cell and for intracellular imaging. The proposed UCNP@PEP probe is a strong blue light emitter (λ max  = 474 nm) upon exposure to an excitation wavelength of 980 nm. The probe was used for detecting Fe 3+ owing to the complexation reaction between UCNP@PEP and Fe 3+ , resulting in reduced upconversion luminescence (UCL) intensity. The proposed probe has a detection limit of 0.2 μM and a good linear range of 1-10 μM for sensing Fe 3+ ions. Moreover, the UCNP@PEP probe displays high cell viability (90%) and is feasible for intracellular imaging. The ability of the probe to sense Fe 3+ in a human serum sample was tested and shows promising output for diagnostic purposes. The prepared UCNP@PEP probe was characterized by using UV-visible (UV-Vis) absorption spectrometry, fluorescence (FL) spectrometry, field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR).

The results of applying heterogeneous chemiluminescent analysis for determination of micro-components are generalized, and the possibility of using this method for determination of toxic anions in waters is demonstrated. Anions undergo conversion beforehand, which causes formation of new analytical forms, i.e., derivates being active in chemiluminescent reactions with luminol. If volatile products are generated as analytical forms, they undergo gas extraction from the matrix with detection using a chemiluminescent indicator in the carrier gas stream at the interface gas-liquid (aqueous solution of luminol). Thus, the techniques for determination of Cl, Br, I, ClO, BrO, IO, NO, NO, S, CrO, AsO, Cl and chloramines are developed. The detection limit (DL) is 0.5-5.0 μg/l, and the analysis time is 2-9 min. In another case, products of conversion are sorbed from the solution on a solid sorbent, and detection is carried out by a luminol solution on the solid surface. A series of heteropoly acids (phosphorus, arsenic, silicon, and germanium) and their ion associates with cation surfactants, along with other large anions, are determined in the form of sorbable ion associates. The DL is 0.02-0.7 μg/l, and the analysis time is 30 min. The advantages of application of heterogeneous chemiluminescent analysis over analysis in homogeneous media are indicated, and the prospects for development of the theoretical bases and field of application are demonstrated. [ABSTRACT FROM AUTHOR]

This article was written to serve as an introduction to this issue of the Canadian Journal of Chemistry that honors the contributions to chemistry of Professor D.R. Arnold. It summarizes the observations reported in a communication that appeared in the Journal of the American Chemical Society 30 years ago in June 1973. This historically important communication laid the foundation for his program on the photochemical generation and reactivity of radical ions in solution and also served as a guide for a developing area of interest of many other research groups. [ABSTRACT FROM AUTHOR]

Studying the adsorption behavior of cationic surfactants can help to develop more effective strategies to limit their dispersion in the environment. However, there have few studies on the adsorption of cationic surfactants from the perspective of critical micelle concentration (CMC). In this study, with cetyltrimethylammonium bromide (CTAB) and octadecyl trimethylammonium bromide (OTAB) serving as the model cationic surfactants, the effect of CMC on the adsorption behavior of cationic surfactant onto the surface of sodium alginate/silica (SA/SiO 2 ) microspheres was systematically revealed. The adsorption mechanism relative to CMC was investigated under different conditions, including surfactant concentration, pH, temperature, and adsorption time. The results suggest that at identical concentrations, the smaller the CMC value of the cationic surfactants, the greater the adsorption amount (q t ). q t for CTAB and OTAB were 583.2 and 678.0 mg/g respectively, with the concentration higher than their CMC value. When the concentration was lower than the CMC value of the cationic surfactants, q t for CTAB and OTAB were 123.2 and 138.7 mg/g, respectively. The CMC value of CTAB was lower than that of OTAB under identical conditions, suggesting that the adsorption of cationic surfactants is related to their CMC. These results are beneficial for the removal of cationic surfactants by adsorption methods., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Developing the delivery systems with high therapeutic efficacy and low side effects is of great interest and significance for anticancer therapy. Compared to the high cost in synthesizing new chemotherapeutic drugs, exploring the anticancer potentials of existing chemicals is more convenient and efficient. Sodium bicarbonate (BC), a simple inorganic salt, has shown its tumor inhibition capacity via regulating the acidity of tumor microenvironment. However, the effects of intracytoplasmic BC on tumor growth and the potentials of BC to serve as an anticancer agent are still unknown. Herein, we developed a BC-loaded cationic liposome system (BC-CLP) to deliver BC into the cytosol of cancer cells. The in vitro studies showed that the BC-CLP containing 1% BC (w/v) had a size of 112.9 nm and a zeta potential of 19.1 mV, which reduced the viability of the model cancer cells (human oral squamous cell carcinoma HSC-3 cells) to 13.7%. In contrast, the neutral BC-LP caused less than 50% viability reduction. We further found that BC-CLP released BC directly into cytoplasm via membrane fusion pathway rather than endocytosis, leading to the remarkable increase of cytosolic pH, which may contribute to the anticancer effect of BC-CLP. Our findings indicate that BC-CLP is a potential system for high-efficiency cancer therapy without causing drug-related side effects or resistance., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Antiphase bursting related to the rhythmic motor behavior exhibits complex dynamics modulated by the inhibitory synaptic current (Isyn), especially in the presence of the hyperpolarization-activated cation current (Ih). In the present paper, the dynamics of antiphase bursting modulated by the Ih and Isyn is studied in three aspects with a theoretical model. Firstly, the Isyn and the slow Ih with strong strength are the identified to be the necessary conditions for the antiphase bursting. The dependence of the antiphase bursting on the two currents is different for low (escape mode) and high (release mode) threshold voltages (Vth) of the inhibitory synapse. Secondly, more detailed co-regulations of the two currents to induce opposite changes of the bursting period are obtained. For the escape mode, increase of the Ih induces elevated membrane potential of the silence inhibited by a strong Isyn and shortened silence duration to go beyond Vth, resulting in reduced bursting period. For the release mode, increase of the Ih induces elevated tough value of the former part of the burst modulated by a nearly zero Isyn and lengthen burst duration to fall below Vth, resulting in prolonged bursting period. Finally, the fast-slow dynamics of the antiphase bursting are acquired. Using one-and two-parameter bifurcations of the fast subsystem of a single neuron, the burst of the antiphase bursting is related to the stable limit cycle, and the silence modulated by a strong Isyn to the stable equilibrium to a certain extent. The Ih mainly modulates the dynamics within the burst and quiescent state. Furthermore, with the fast subsystem of the coupled neurons, the silence is associated with the unstable equilibrium point. The results present theoretical explanations to the changes in the bursting period and fast-slow dynamics of the antiphase bursting modulated by the Isyn and Ih, which is helpful for understanding the antiphase bursting and modulating rhythmic motor patterns. [ABSTRACT FROM AUTHOR]

β-lactoglobulin (BLG) is the major whey protein with negative charges at neutral pH in aqueous media. Thus, the interaction with mucins, the major polyanionic component of mucus, is very weak due to the electrostatic repulsion between them. The present study postulates that cationization of BLG molecules may reverse the interaction characteristics between BLG and mucin from repulsive to associative. To this end, cationic-modified BLGs were prepared by grafting positively charged ethylenediamine (EDA) moieties into the negatively charged carboxyl groups on the aspartic and glutamic acid residues and compared with non-modified BLG upon mixing with porcine gastric mucin (PGM). To characterize the structural and conformational features of PGM, non/cationized BLGs, and their mixtures, various spectroscopic approaches, including zeta potential, dynamic light scattering (DLS), and circular dichroism (CD) spectroscopy were employed. Importantly, we have taken surface adsorption with optical waveguide lightmode spectroscopy (OWLS), and tribological properties with pin-on-disk tribometry at the sliding interface as the key approaches to determine the interaction nature between them as mixing PGM with polycations can lead to synergistic lubrication at the nonpolar substrate in neutral aqueous media as a result of an electrostatic association. All the spectroscopic studies and a substantial improvement in lubricity collectively supported a tenacious and associative interaction between PGM and cationized BLGs, but not between PGM and non-modified BLG. This study demonstrates a unique and successful approach to intensify the interaction between BLG and mucins, which is meaningful for a broad range of disciplines, including food science, macromolecular interactions, and biolubrication etc., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Nucleic acid delivery by viral and non-viral methods has been a cornerstone for the contemporary gene therapy aimed at correcting the defective genes, replacing of the missing genes, or downregulating the expression of anomalous genes is highly desirable for the management of various diseases. Ostensibly, it becomes paramount for the delivery vectors to intersect the biological barriers for accessing their destined site within the cellular environment. However, the lipophilic nature of biological membranes and their potential to limit the entry of large sized, charged, hydrophilic molecules thus presenting a sizeable challenge for the cellular integration of negatively charged nucleic acids. Furthermore, the susceptibility of nucleic acids towards the degrading enzymes (nucleases) in the lysosomes present in cytoplasm is another matter of concern for their cellular and nuclear delivery. Hence, there is a pressing need for the identification and development of cationic delivery systems which encapsulate the cargo nucleic acids where the charge facilitates their cellular entry by evading the membrane barriers, and the encapsulation shields them from the enzymatic attack in cytoplasm. Cycloamylose bearing a closed loop conformation presents a robust candidature in this regard owing to its remarkable encapsulating tendency towards nucleic acids including siRNA, CpG DNA, and siRNA. The presence of numerous hydroxyl groups on the cycloamylose periphery provides sites for its chemical modification for the introduction of cationic groups, including spermine, (3-Chloro-2 hydroxypropyl) trimethylammonium chloride (Q188), and diethyl aminoethane (DEAE). The resulting cationic cycloamylose possesses a remarkable transfection efficiency and provides stability to cargo oligonucleotides against endonucleases, in addition to modulating the undesirable side effects such as unwanted immune stimulation. Cycloamylose is known to interact with the cell membranes where they release certain membrane components such as phospholipids and cholesterol thereby resulting in membrane destabilization and permeabilization. Furthermore, cycloamylose derivatives also serve as formulation excipients for improving the efficiency of other gene delivery systems. This review delves into the various vector and non-vector-based gene delivery systems, their advantages, and limitations, eventually leading to the identification of cycloamylose as an ideal candidate for nucleic acid delivery. The synthesis of cationic cycloamylose is briefly discussed in each section followed by its application for specific delivery/transfection of a particular nucleic acid., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The coexistence of metal cations is often accompanied by organic pollution and could affect the environmental fate of organics by mediating the formation of cation bridges. However, the environmental fate and risk of organics in cation co-existing environments are poorly understood due to the lack of accurate identification of cation bridge formation and stability. In this study, the sorption of sulfamethoxazole (SMX) on montmorillonite (MT) with the coexistence of three different valence metal cations (Na + , Ca 2+ , and Cr 3+ ) was investigated. Ca 2+ and Cr 3+ can significantly promote the sorption of SMX on MT for about 5∼10 times promotion, respectively, while Na + bridges displayed little effect on the sorption of SMX. The sorption binding energy of SMX with MT-Ca (-44.01 kcal/mol) and MT-Cr (-64.57 kcal/mol) bridges was significantly lower than that with MT-Na (-38.45 kcal/mol) and MT (-39.39 kcal/mol), indicating that the sorption affinity of SMX on Cr and Ca bridges was much stronger. The higher valence of the cations also resulted in a more stable adsorbed SMX with less desorption fluctuation. In addition, the relatively higher initial concentration of SMX and the valence of cations increased the bonding density of the cation bridges, thus promoting the apparent sorption of SMX on MT to a certain extent. This work reveals the formation and function of cation bridges in the sorption of SMX on MT. It lays a theoretical foundation for further understanding the environmental fate and risk of organics., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The aging process of microplastics (MPs) could significantly change their physical and chemical characteristics and impact their migration behavior in soil. However, the complex effects of different cations and humic acids (HA) on the migration of aged MPs through saturated media are not clear. In this research, the migration and retention of pristine/aged PSMPs (polystyrene microplastics) under combined effects of cations (Na + , Ca 2+ ) (ionic strength = 10 mM) and HA (0, 5, 15 mg/L) were investigated and analyzed in conjunction with the two-site kinetic retention model and DLVO theory. The findings showed that the aging process accelerated PSMPs migration under all tested conditions. Aged PSMPs were less susceptible to Ca 2+ than pristine PSMPs. Under Ca 2+ conditions, pristine/aged PSMPs showed higher retention than under Na + conditions in the absence of HA. Furthermore, under Na + conditions, the migration of aged PSMPs significantly increased at higher concentrations of HA. However, under Ca 2+ conditions, the migration of aged PSMPs decreased significantly at higher concentrations of HA. In higher HA conditions, HA, Ca 2+ , and PSMPs interact to cause larger aggregations, resulting in the sedimentation of aged PSMPs. The DLVO calculations and two-site kinetic retention models' results showed the detention of PSMPs was irreversible under higher HA conditions (15 mg/L) with Ca 2+ , and aged PSMPs were more susceptible to clogging. These findings may help to understand the potential risk of migration behavior of PSMPs in the soil-groundwater environment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

A series of laboratory experiments are conducted to simulate the acidification and subsequent recovery of a sand aquifer exploited by in situ recovery (ISR) mining. A sulfuric acid solution (pH 2) is first injected into a column packed with sand from the Zoovch Ovoo uranium roll front deposit (Mongolia). Solutions representative of local groundwater or enriched in cations (Na + , Mg 2+ ) are then circulated through the column to simulate the inflow of aquifer water. pH and major ion concentrations (Na + , Cl - , SO 4 2- , Ca 2+ , Mg 2+ ) measured at the column outlet reproduce the overall evolution of porewater chemistry observed in the field. The presence of minor quantities of swelling clay minerals (≈6 wt% smectite) is shown to exert an important influence on the behavior of inorganic cations, particularly H + ) measured at the column outlet reproduce the overall evolution of porewater chemistry observed in the field. The presence of minor quantities of swelling clay minerals (≈6 wt% smectite) is shown to exert an important influence on the behavior of inorganic cations, particularly H + , via ion-exchange reactions. Numerical models that consider ion-exchange on smectite as the sole solid-solution interaction are able to reproduce variations in pH and cation concentrations in the column experiments. This highlights the importance of clay minerals in controlling H + mobility and demonstrates that sand from the studied aquifer can be described to a first order as an ion-exchanger. The present study confirms the key role of clay minerals in controlling water chemistry in acidic environments through ion-exchange processes. In a context of managing the long-term environmental footprint of industrial and mining activities (ISR, acid mine drainage…), this work will bring insights for modeling choices and identification of key parameters to help operators to define their production and/or remediation strategies., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

It is important to study the steel corrosion inhibition behavior in complex chloride salt environments. This paper uses the fact that calcined layered double hydroxides (CLDHs) have a certain memory effect, which means that it can reabsorb water and anions and partially restore the lamellar structure under certain conditions. This work investigated the influence of cation types on the steel corrosion inhibition behavior of CLDH in saturated calcium hydroxide solution using equilibrium isotherms of Cl− uptake, the electrochemical method, X-ray diffraction (XRD), Fourier-transform infrared (FTIR), and scanning electron microscopy (SEM) techniques. The results show that the corrosion inhibition of the CLDH is affected by the cation types in the following order: Ca2+>Mg2+>K+≈Na+·Na+ and K+ increase the pH of the solution and decrease the corrosion inhibition of CLDH. The addition of Mg2+ can promote the reconstruction of Mg-Al-Zn-Cl hydrotalcite. The addition of Ca2+ can promote the formation of new Ca-Al layered double hydroxide (Ca-Al-LDH) and improve the corrosion inhibition. [ABSTRACT FROM AUTHOR]

Waxy maize contains nearly 100% of the branched amylopectin type of starch, which has a similar structure to that of a commercial anionic organic micro-particle (OMP). It was found that the maize starch would have the same function as the OMP if carboxymethyl groups were introduced; moreover, the performance of carboxymethyl starch as a retention and drainage aid could be enhanced by grafting some cationic groups on the backbone of the starch so that it could absorb on fibers through electrostatic attraction. In this study, the introduced groups of cationic-modified carboxymethyl starch (CCMS) prepared from waxy maize were determined by FT-IR and ¹H NMR spectroscopy. Factors affecting retention and drainage, comparison between CCMS and OMP systems, and also the strengthening effect of CCMS were studied. The results showed that CCMS had excellent performance when it was used with cationic polyacrylamide (CPAM) as a retention system. Compared with the OMP, CCMS had better retention performance when the dosage was in the range from 0.01% to 0.08%, and it yielded much more uniform formation of the handsheets. Additionally, CCMS had a strengthening effect on the paper, which distinguished it from other retention aids. [ABSTRACT FROM AUTHOR]

• The mechanism of organic electrode weakening self-discharge effect of dual-ion battery was explored. • The performance of metal-free dual-ion batteries in different ionic liquid electrolytes was investigated. • The method of reducing the dissolution of organic electrode in ionic liquid electrolyte was discussed. The strong self-discharge reaction is one of the key factors limiting the practical use of dual-ion batteries, which leads to low coulombic efficiency and discharge capacity loss. It is of great significance to effectively reduce the self-discharge effect through redox reactions between organic electrodes and electrolytes. Herein, a dual-ion battery study that uses 1,4,5,8-naphthalenetetracarboxylic dianhydride as the anode and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide as the electrolyte is conducted. Due to the introduction of organic materials, the storage mechanism of cations on the anode is changed, which weakens the self-discharge effect. The battery shows a low self-discharge rate of 6.12% h−1 and a high discharge capacity of 114 mAh g−1. The voltage declines by only 0.14 V after resting for 15 h due to the strong redox reaction between Pyr 14 + cations and the C O groups of NTCDA. Meanwhile, a double-layer filter paper system with small porosity is used to improve the cycle performance of the battery. [ABSTRACT FROM AUTHOR]

In the past 20 years, perovskite-related research has attracted wide attention. The related research into two-dimensional/quasi-two-dimensional perovskite has propelled the research of perovskite materials to a new height. To improve the properties of quasi-2D perovskite, improve the stability of materials, and achieve specific functions, using different types, volumes, and lengths of organic spacers is an essential method. In this paper, quasi-2D perovskites with EDA (ethylene diammonium), PDA (1,3-propanediammonium), and BDA (1,4-butanediammonium) (m = 2–4) as organic spacers were prepared, and the effects of different organic spacers on the 2D perovskite were investigated. The results show that the length of the organic spacer significantly impacts the perovskite's properties. A shorter organic spacer can effectively reduce the quantum confinement and dielectric confinement in perovskite. It should be noted that if the organic spacer is too short, the stability of the quasi-2D perovskite will be greatly reduced. [ABSTRACT FROM AUTHOR]

A superatom is a cluster of atoms that acts like a single atom. Two main groups of superatoms are superalkalis and superhalogens, which mimic the chemistry of alkali and halogen atoms, respectively. The ionization energies of superalkalis are smaller than those of alkalis (<3.89 eV for cesium atom), and the electron affinities of superhalogens are larger than that of halogens (>3.61 eV for chlorine atom). Exploring new superalkali/superhalogen aims to provide reliable data and predictions of the use of such compounds as redox agents in the reduction/oxidation of counterpart systems, as well as the role they can play more generally in materials science. The low ionization energies of superalkalis make them candidates for catalysts for CO2 conversion into renewable fuels and value-added chemicals. The large electron affinity of superhalogens makes them strong oxidizing agents for bonding and removing toxic molecules from the environment. By using the superatoms as building blocks of cluster-assembled materials, we can achieve the functional features of atom-based materials (like conductivity or catalytic potential) while having more flexibility to achieve higher performance. This feature paper covers the issues of designing such compounds and demonstrates how modifications of the superatoms (superhalogens and superalkalis) allow for the tuning of the electronic structure and might be used to create unique functional materials. The designed superatoms can form stable perovskites for solar cells, electrolytes for Li-ion batteries of electric vehicles, superatomic solids, and semiconducting materials. The designed superatoms and their redox potential evaluation could help experimentalists create new materials for use in fields such as energy storage and climate change. [ABSTRACT FROM AUTHOR]

In fair weather, the vertical atmospheric electric field is oriented downward (positive in the earth surface ordinate system) in the global atmospheric circuit. Some researchers have revealed the unique phenomenon whereby once an upward vertical atmospheric electric field is observed in fair weather, an earthquake (EQ) follows within 2–48 h regardless of the EQ magnitude. However, the mechanism has not been explained with a suitable physical model. In this paper, a physical model is presented considering four types of forces acting on charged particles in the air. It is demonstrated that the heavier positive ions and lighter negative ions are rapidly separated. Finally, a reversed fair weather electrostatic field is formed by the above charge separation process. The simulation results have instructive significance for future observations and hazard predictions and still need further research. [ABSTRACT FROM AUTHOR]

Forest riparian zones are a major in control of surface water quality. Base cation (BC) concentrations, fluxes, and cycling in the riparian zone merit attention because of increasing concern of negative consequences for re-acidification of surface waters from future climate and forest harvesting scenarios. We present a two-year study of BC and silica (Si) flow-weighted concentrations from 13 riparian zones and 14 streams in a boreal catchment in northern Sweden. The Riparian Flow-Concentration Integration Model (RIM) was used to estimate riparian zone flow-weighted concentrations and tested to predict the stream flow-weighted concentrations. Spatial variation in BC and Si concentrations as well as in flow-weighted concentrations was related to differences in Quaternary deposits, with the largest contribution from lower lying silty sediments and the lowest contribution from wetland areas higher up in the catchment. Temporal stability in the concentrations of most elements, a remarkably stable Mg /Ca ratio in the soil water and a homogeneous mineralogy suggest that the stable patterns found in the riparian zones are a result of distinct mineralogical upslope groundwater signals integrating the chemical signals of biological and chemical weathering. Stream water Mg /Ca ratio indicates that the signal is subsequently maintained in the streams. RIM gave good predictions of Ca, Mg, and Na flow-weighted concentrations in headwater streams. The difficulty in modelling K and Si suggests a stronger biogeochemical influence on these elements. The observed chemical dilution effect with flow in the streams was related to variation in groundwater levels and element concentration profiles in the riparian zones. This study provides a first step toward specific investigations of the vulnerability of riparian zones to changes induced by forest management or climate change, with focus on BC or other compounds. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Kirkuk University for Agricultural Sciences is the property of Republic of Iraq Ministry of Higher Education & Scientific Research (MOHESR) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The Cairns-distributed electrons and positive ions in a plasma made up of a negative dust fluid are taken into account to examine the presence of arbitrary amplitude dust-acoustic solitons. It has previously been noted that nonthermal ions and thermal electrons generate both compressive and rarefactive solitons. In this paper, we noticed that nonthermal electrons together with nonthermal ions are responsible for producing the rarefactive solitons. It is found that the Sagdeev potential strongly depends on plasma parameters, such as nonthermal index α and Mach number, which, in turn, influence the Sagdeev potential and solitons significantly. We also found that the critical match number and height of soliton increase with the nonthermal parameter α. We further note that the Sagdeev potential as a function of potential φ becomes more negative and the amplitude of the soliton also enhances as the value of Mach number rises. It is concluded that the model presented here based on nonthermal ions and electrons in a negative dust fluid provides a worthy interpretation for electrostatic solitons observed in space plasmas. [ABSTRACT FROM AUTHOR]

The tip size of metal protrusions is an important factor affecting corona discharge, since it influences the electric filed, the ionization range and strength around the protrusion defect. Most existing studies on the influence of protrusion tip size on corona discharge are implemented by experimental methods. However, these studies are difficult to obtain the microphysical process of charged particles, which is related to the generation of current pulses and electromagnetic (EM) waves. In this paper, a hydrodynamic simulation model is proposed to study the effect of protrusion tip size on the microphysical process and current pulses of negative corona discharge. A mapping relationship between microscopic behaviors of charged particles and current pulses is established by this simulation method. Based on the comparison of microphysical quantities, the effect of defect tip size on the detailed parameters of current pulses is clearly explained. It shows that with the increase of tip size under a constant voltage, all the five parameters of current pluses increase. The rising time is related to the effective ionization coefficient, while the falling time is dependent on the velocities of positive and negative ions. The experiment and simulation results coincide in current waveforms and all five parameters. [ABSTRACT FROM AUTHOR]

Supercapacitors have many applications in new energy and other high-tech fields. The desolvation effect on ions affects the capacity size of supercapacitors, and there are few relevant studies published in this field at present. In this experiment, bilayer graphene (BG) with a layer spacing of 4–10 Å was used as a model of flat pores and was calculated with first-principles calculations, which can effectively simulate the adsorption behaviour of porous carbon. The reaction energies of ions, propylene carbonate, and ionic complexes in bilayer graphene with different layer spacings were calculated, and the desolvation behaviour of lithium salt cations (Li+), tetraethyl quaternary ammonium salt cations (TEA+), triethyl methyl quaternary ammonium salt cations (TEMA+), and bipyrrolidinium quaternary ammonium salt cations (SBP+) was investigated. The calculation was based on density functional compact bound (DFTB+) software. The calculated results show that in the stacked system, the complete desolvation size of the TEA+ reaches 5.6 Å, the complete desolvation size of the TEMA+ reaches 4.9 Å, the complete desolvation size of the SBP+ reaches 4.8 Å, and the complete desolvation size of the Li+ reaches 5.4 Å, with the organic electrolyte cations showing a positive trend in the complete desolvation size as the ion radius increases. An in-depth analysis of the data shows that Li+, TEA+, TEMA+, and SBP+ ion radii play a dominant role in the size of desolvation. The results of this paper provide an effective aid for the selection of organic electrolytes to increase the capacity of supercapacitors. [ABSTRACT FROM AUTHOR]

Copyright of Food Research & Development is the property of Food Research & Development Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Static time-of-flight secondary ion mass spectrometry (ToF-SIMS) was performed for acquiring the high-resolution surface spectra of four types of synthesized imidazolium ionene membranes. These novel membranes have aromatic ether–ketone–ether linkages inspired by poly(ether ether ketone) (PEEK). The PEEK-ionenes synthesized for this study have imidazolium cations placed in the polymeric backbone with bistriflimide [Tf2N]− counterions. The attention given to synthetically modified PEEK derivatives, such as PEEK-ionenes, is considerable due to their ability to selectively capture CO2 molecules and other light gases. Therefore, it is important to characterize the surface of these synthesized novel PEEK-ionenes. In this work, characteristic and unique peaks were identified in the positive spectra of each sample. The differences in mass spectra among the samples provide insights for optimizing or fine-tuning the PEEK-ionenes synthesis to achieve a high-performance CO2 separation membrane with enhanced permeability, selectivity, and mechanical stability. The SIMS spectra and identified characteristic peaks of these synthesized ionenes will serve as a reference in the positive mode, complementing the corresponding spectra reported in the negative ion mode (Paper II). [ABSTRACT FROM AUTHOR]

Plasma jet normally operates in a regime of positive or negative streamers. Different propagating behaviors have been investigated for positive streamers. However, there are few studies on negative streamers. In this paper, a two-dimensional fluid model is used to simulate the behavior of a negative streamer encountered with a cloud of positive ions. Simulation results indicate that the negative streamer behaves like a free streamer when the ion cloud has a low charge density. After initiation near the needle tip, the streamer propagates along the axis, passes through the ion cloud, and finally reaches the anode vicinity along a straight line. When the streamer reaches the ion cloud, its head radius (R0) is investigated as a function of parameters, including the voltage amplitude and the gap width, as well as the charge density, axial position, and spatial size of the ion cloud. At a given moment, electric field strength and electron density near the streamer head increase with increasing charge density of the ion cloud. In the case of a high charge-density ion cloud, after a primary streamer propagates some distance along the axis, a positive secondary streamer, and a negative secondary streamer start to propagate from the cloud to the cathode and the anode, respectively. [ABSTRACT FROM AUTHOR]

Supercapacitors have a wide range of applications in high-technology fields. The desolvation of organic electrolyte cations affects the capacity size and conductivity of supercapacitors. However, few relevant studies have been published in this field. In this experiment, the adsorption behavior of porous carbon was simulated with first-principles calculations using a graphene bilayer with a layer spacing of 4–10 Å as a hydroxyl-flat pore model. The reaction energies of quaternary ammonium cations, acetonitrile, and quaternary ammonium cationic complexes were calculated in a graphene bilayer with different interlayer spacings, and the desolvation behavior of TEA+ and SBP+ ions was described. The critical size for the complete desolvation of [TEA(AN)]+ was 4.7 Å, and the partial desolvation size ranged from 4.7 to 4.8 Å. The critical size for the complete desolvation of [SBP(AN)]+ was 5.2 Å, and the partial desolvation size ranged from 5.2 to 5.5 Å. As the ionic radius of the quaternary ammonium cation decreased, the desolvation size showed a positive trend. A density of states (DOS) analysis of the desolvated quaternary ammonium cations embedded in the hydroxyl-flat pore structure showed that the conductivity of the hydroxyl-flat pore was enhanced after gaining electrons. The results of this paper provide some help in selecting organic electrolytes to improve the capacity and conductivity of supercapacitors. [ABSTRACT FROM AUTHOR]

[Display omitted] • Chromogenic sensor for selective estimation of aqueous ferric ions was developed. • The chromogenic paper strip was prepared via doping tannic onto filter paper. • A visible color shift from white to purple was observed in the presence of Fe(III). • A concentration range of 10–190 ppm was monitored a detection limit of Fe(III). • The current sensor is a simple and practical tool for real-time detection of Fe(III). Investigation of chromogenic sensor which can selectively estimate ferric cations in aqueous environment with prospect to produce portable platforms is currently proposed. Herein, the chromogenic sensor (Tannic Acid@Filter Paper; TA@FP) was prepared via doping of tannic acid within filter paper to afford the excellent selectivity for ferric cations over various examined metal ions. The designed chromogenic sensor was applied for estimating ferric ions via turn-on detection, while, it could acquire a marked visible color shifting from white to purple hue depending on the total content of Fe (III) ions in the aqueous medium. Complete characterization of the designed sensor before and after its exploitation in estimation of ferric cations was systematically performed via different spectral and microscopic analyses. The functionalized TA@FP was quite sensitive for quantitative estimation of ferric ions with wide scaling linear concentration range of 10–190 ppm. Maximum sensitivity of the exploited platform was observed at very low concentration (10 ppm) rather than the higher concentrations. The correlation coefficient (R2 = 0.99) was closer to unity. The prepared chromogenic sensor could be described as a simple and practical sensing tool for real-time quantitative and qualitative assessment of Fe (III) cations. [ABSTRACT FROM AUTHOR]

Paper-capillary spray modified on the basis of paper spray ionization in order to facilitate the combination with portable mass spectrometry is an ambient ionization technique, which can be uesd to detect compounds rapidly without the restriction of location and environment. Paper-capillary spray and ambient ionization portable mass spectrometry in positive ion mode were used to collect mass spectrum information of 40 kinds of cathinones controlled in China. The ［M+H］+ peak of MS1, the characteristic fragment ions of MS2 and MS2_DDA mode and their relative abundance ratio were analyzed. The obtained mass spectrum information was used to establish a database for the rapid screening of 40 cathinones. It was found that C—N cleavage at the α site existed in all the cathinones through the study of their fragmentation characteristics. Whether the highest ion peak was ［M—H2O+H］+ fragment peak could infer the existence of secondary and tertiary amine structures. A series of characteristic peaks of m/z 98+CnH2n would exist when the N was substituted by pyrrolidinyl. The characteristic ion of ［M+H］+ lost 48 u or that of non ［M+H］+ lost 30 u would exist when the benzene ring was substituted by methylenedioxy. The fragmentation characteristics were studied to design and establish a complete analysis strategy for the unknown cathinones. The strategy could be applied in the following three aspects. 1) To judge whether they are cathinones; 2) To judge whether they are 40 kinds of cathinones in the database; 3) To infer the characteristic structure of cathinones outside the scope of the database. The strategy was successfully used for the structural identification of 10 analytes, which included the common categories of drugs controlled in China. No interference or misjudgment was found, and the database could be used normally. The structures inferred by the analysis strategy were consistent with the actual structure, and the isomers involved would also be distinguished because of their different fragment ions, indicating that this scheme was feasible. This method only needs simple sample loading operation and integrated small mass spectrometer, and is not limited by location and environment. In the investigation of such drug cases, this method can carry out rapid screening and timely feedback, which plays an important role in the rapid and accurate crackdown on the crime of cathinones and it is expected to be a new way to study and judge the crime of cathinones. [ABSTRACT FROM AUTHOR]

The Solar Wind Ion Focusing Thruster (SWIFT) is a highly-innovative propellantless propulsion concept, recently proposed by Gemmer and Mazzoleni. In its nominal configuration, a SWIFT consists of a conically-shaped mesh of positively-charged conducting tethers, with its vertex linked to the spacecraft and its axis oriented towards the Sun. The SWIFT collects and filters the solar wind plasma and suitably directs the positive ions, which are then accelerated by an ion thruster. Such a device is theoretically able to generate a deep-space propulsive acceleration that comes, in part, from the solar wind dynamic pressure impinging on the conical grid and, in part, from the positive ion beam. In particular, the orientation of the ion beam may be chosen in such a way as to set the resultant propulsive acceleration and steer the spacecraft. The aim of this paper is to analyze the performance of a SWIFT-propelled spacecraft in an orbit-to-orbit two-dimensional interplanetary transfer. To that end, some mission scenarios are studied, in an optimal framework, by minimizing the total flight time necessary for the spacecraft to complete the transfer as a function of the propulsion system performance parameters. Numerical simulations are used to compare the optimal flight times calculated in simplified Earth–Venus and Earth–Mars transfers with those obtained by considering other propellantless propulsion systems. [ABSTRACT FROM AUTHOR]

Mixtures of powder and liquid are ubiquitous in nature as well as industries and exhibit complex flowing and deforming behaviors, including sol to gel transition under shear stress. In order to better understand the characteristic features of this type of mixture, we observed the behavior of a mixture of colloidal silica particles and water as a model system under vibration. The mixture showed different states, from powder-like to viscous fluid-like, with increasing content of water. At certain concentrations of silica particles (around 70 wt. %) and under relatively faster vibration (over 17 Hz), we observed that the colloidal suspension of silica particles and water climbed up the wall of a container against gravity. The main purpose of this paper is to report how we can observe the climbing suspension of colloidal silica. The rheological measurements of the climbing suspension demonstrated that the climbing suspension showed shear-thickening behavior, where force chain networks and normal stress differences are considered to develop. Therefore, we speculate that the transient formation and breaking of force networks and normal stress differences under vibration contribute to the occurrence of the climbing suspension. The tunable nature of colloidal suspensions may help to elucidate the climbing mechanism in the future. [ABSTRACT FROM AUTHOR]

An hourly scale precursor of inland earthquakes (EQs) is revealed in this paper. Several EQ cases in China have been reported. As indicated by a table listing 23 inland EQs and their shock time, epicenter location, magnitude, near-epicenter weather conditions, precursor start time and precursor duration, when the weather conditions are fair near the epicenter, an anomalously negative atmospheric electrostatic signal is readily observable approximately 2–48 h before the EQ occurs. Moreover, a successful single-station alarm for nearby moderate-magnitude EQs is demonstrated, and a possible mechanism for the precursor signal is proposed. The change in the electrostatic field during an EQ process is explained as the release of radioactive gases from the subsurface into the atmosphere via large (regional-scale) preexisting microfractures in the rock at the source depth. These gases considerably ionize the atmosphere, and the separated positive and negative ions establish a special macroscopic electric field. The final critical stage of 2–48 h before an EQ may indicate a stable tectonic process. [ABSTRACT FROM AUTHOR]