Reactive Ion Research Articles

Kinetic, Thermodynamic, and Dynamic Control in Normal vs. Cross [2 + 2] Cycloadditions of Ene-Keteniminium Ions: Computational Understanding, Prediction, and Experimental Verification

Almost all reported intramolecular [2 + 2] reactions of ene-keteniminium ions gave normal [2 + 2] products with a fused bicycle framework, but not cross [2 + 2] products with a bicyclo[3.1.1]heptane skeleton, a highly pursued bioisostere in pharmaceutical chemistry. How to rationalize this and design new cross [2 + 2] reactions? Theoretical studies using density functional theory, high-level ab initio single-point energy calculations, and molecular dynamics showed that this [2 + 2] reaction has all three patterns of regiochemical control: the reaction is controlled either kinetically, thermodynamically, or dynamically. A carbocation model of forming endo and exo carbocations has been proposed to rationalize the reaction outcomes, revealing that the tethers (between alkenes and keteniminium ions), substituents (on the alkenes), and alkene configurations in ene-keteniminium ions play critical roles. These understandings were further used to predict that introducing a substituent in the terminal position of alkene with a trans configuration in ene-keteniminium ions can realize the cross [2 + 2] reaction, which is dynamically controlled for alkyl substituents or kinetically controlled for aryl substituents. These and more other predictions were realized experimentally, and many cross [2 + 2] products with a bicyclo[3.1.1]heptane skeleton can be achieved. Both molecular dynamics and new experiments have also been applied to correct a key but misassigned [2 + 2] product reported in the literature, further supporting the insightful mechanisms reported here.

Characterizing the removal of Pb2+ and Zn2+ from an acidic smelting wastewater using electrocatalytic internal Fe0/C micro-electrolysis

The discharge of acid non-ferrous metal smelting wastewater has received unprecedented attention with increasing threat to ecosystems and human health. A combined process of electrocatalytic internal Fe0/C micro-electrolysis (ECIME) fluidized bed was developed at lab scale (2.0L) to investigate the co-removal performance, optimization conditions and reaction characteristics differences of Pb2+ and Zn2+ from acid smelting wastewater. The results of cyclic voltammogram (CV) and XPS reveal that Pb2+ and Zn2+ can be electrodeposited on the carbon microelectrodes surface in ECIME system, and the positive shift degree of the reductive peak potentials under cathodic polarized is positively correlated with the voltage intensity. Metal ions reaction flow direction of ECIME system and SEM, EDS, XPS characterizations indicated that the removal of Pb2+ and Zn2+ were mainly attribute to electroreduction deposition and in-situ iron polymer hydroxyl flocculation, and including four reaction processes of electroreduction on surface of external electrode, iron-carbon particles microelectrode, self-flocculation and secondary flocculation. But the removal of Pb2+ and Zn2+ show different dominant reaction path, Pb2+ removal mainly depended on the electroreduction deposition (64.11%), whereas Zn2+ dominated by iron-based flocculation (62.93%). Response surface optimization based on the average efficiency indicated that the co-removal of Pb2+ and Zn2+ mainly depended on polarization voltage, reaction time, initial pH and electrolyte concentration with optimal conditions of 11.0 V, 58.65 min, 5.0, and 0.08 mol/L, and its optimal average removal efficiency reached 98.52% (initial concentration 100 mg/L), and the residual concentrations were 0.081 mg/L and 1.890 mg/L, respectively. These findings provide insights and theoretical for developing electrochemical platform to realize heavy metal wastewater zero discharge.

Electron Transfer Reaction of Theobromine and Permanganate Ion in Aqueous Acidic Media

Electron transfer reaction of theobromine (hereafter referred to as TB) and permanganate ion has been studied using spectrophotometric technique under pseudo first-order conditions at T = 24, [H+] = 3.2 × 10–1 mol dm–3and I = 1.0 mol dm–3 (Na2SO4). Stoichiometric study depicted that two moles of TB were consumed by one mole of permanganate ion. The rate of the reaction is first order in both [TB] and [MnO4-] and second order overall. It was observed that, [H+] and ionic strength respectively enhanced the rate of the reaction in the range studied. Michaelis-Mentens analysis showed no evidence of intermediate complex formation. Added anions and cations were observed to catalyze the reaction rate. The reaction conforms to the rate law as shown below: -d [MnO4-]/dt = (a+b [H+]) [TB] [MnO4-] where a = 0.041 dm3mol–1 s–1 and b= 0.028 dm3mol–1 s–1. The reaction thus occurs by an outer-sphere pathway and plausible mechanism is proposed for the reaction.

Modeling of micellar‐catalyzed bimolecular ionic reactions by a nonlinear Poisson−Boltzmann equation and an electrostatic free energy model

AbstractThe hydrolysis reactions of crystal violet (CV) and p‐nitrophenyl acetate (PNPA) by sodium hydroxide in cetyltrimethylammonium bromide (CTAB) micellar solution were studied in this work. Combined with the Boltzmann probability of ionic species in an electrostatic potential field, a model with a numerical scheme was developed based on the nonlinear Poisson−Boltzmann equation in the micelle‐cell consisting of the reactants and the surfactant. The numerical solution gives the ionic species distribution in the micelle phase and the radius of the micelle‐phase. The dielectric constant of the micelle‐phase varies in the range of 39.8−54.4. The second‐order reaction rate constants in the micelle‐phase were determined using the electrostatic and dipolar free energy models. For the basic hydrolysis of CV and PNPA, the overall second‐order rate constants are three to five times and 1.4 times greater than the corresponding values in water, respectively. The rate enhancement occurs due to the distribution of the reactive ionic species in the cell region and the enhancement of the Coulombic and dipolar interactions among the ionic and polar reactants.

Observing the ping-pong modality of the isospin degree of freedom in cluster emission from heavy-ion reactions

Two-body correlations of the isotope-resolved light and heavy clusters are measured in $^{86}$Kr+$^{\rm 208}$Pb reactions at 25 MeV/u. The yield and kinetic variables of the $A=3$ isobars, triton and $^3$He, are analyzed in coincidence with the heavy clusters of $7\le A \le 14$ emitted at the earlier chance. While the velocity spectra of both triton and $^3$He exhibit scaling behavior over the type of the heavy clusters, the yield ratios of ${\rm t/^3He}$ correlate reversely to the neutron-to-proton ratio $N/Z$ of the latter, showing the ping-pong modality of the $N/Z$ of emitted clusters. The commonality that the $N/Z$ of the residues keeps the initial system value is extended to the cluster emission in heavy ion reactions. The comparison of transport model calculations to the data is discussed.

3D ZnII-Based coordination polymer: Synthesis, structure and fluorescent sensing property for nitroaromatic compounds

A water-stable ZnII-based coordination polymer (CP) with excellent photophysical behavior, namely [Zn2L(atez)(H2O)2] (compound 1; H3L = 4-(2′,3′-dicarboxylphenoxy); atez = 5-aminotetrazole), was successfully prepared by the solvothermal reaction of Zn ions with a π-conjugated and semi-rigid multicarboxylate ligand H3L in the presence of N-containing linker atez. Compound 1 displays a hierarchically pillared three-dimensional (3D) (3,4,5)-connected (4·62) (42·64) (43·64·83) net which is based on two-dimensional (2D) multicarboxylate- ZnII layers strutted by the atez ligands. Sensing investigations of compound 1 reveal that this material can selectively and sensitively detect nitroaromatic compounds in water suspension through fluorescence quenching effect. In particular, it is worth noting that it shows highly specific detection of nitrobenzene (NB) and 2,4,6-trinitrophenol (TNP) with remarkable quenching constants (KSV = 7.5 × 104 M−1 for NB and KSV = 1.9 × 105 M−1 for TNP) and low limit of detection (LOD = 0.93 μM for NB and LOD = 0.36 μM for TNP). Investigations reveal that the probable mechanisms for such sensing processes are the concurrent presence of fluorescence resonance energy transfer (FRET) as well as photoinduced electron transfer (PET) between the CP and nitroaromatic molecules. This work not only offers an effective route to improve the application of fluorescent CPs but also provide one novel probable fluorescence probe for nitroaromatic compounds.

Direct determination of five xanthic acids in water by ultra performance liquid chromatography-tandem mass spectrometry

Xanthates with different alkyl groups, such as ethyl, propyl, butyl, and amyl groups, are widely used in large quantities in the mining flotation of metallic minerals. Xanthates enter environmental waters through mineral processing wastewater discharge and are ionized or hydrolyzed into ions or molecules of xanthic acids (XAs) in water. XAs endanger aquatic plants and animals, as well as human health. To the best of our knowledge, XA analysis is mainly limited to butyl xanthate. Moreover, the isomers and congeners of XAs cannot be determined separately using the existing methods. Herein, a novel method based on ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established to separate and analyze five XAs, namely, ethyl-, isopropyl-, n-butyl-, isobutyl-, and amyl-XAs, in water. Water samples were filtered through a 0.22 μm hydrophilic polytetrafluoroethylene (PTFE) membrane and directly injected into the UPLC-MS/MS instrument. Separation was performed using a Waters Acquity UPLC BEH C18 column (100 mm×2.1 mm, 1.7 μm) with ammonia solution (pH 11)-acetonitrile (9∶1, v/v) as the mobile phase for isocratic elution. The five XAs were detected in the negative electrospray ionization (ESI-) and multiple reaction monitoring (MRM) modes. An internal standard method was used for quantification. The pretreatment and UPLC-MS/MS conditions were comprehensively optimized to achieve the separation and analysis of the five XAs via direct injection. The XAs showed negligible adsorption on hydrophobic PTFE, hydrophilic PTFE, hydrophilic polypropylene, and polypropylene membranes during filtration. However, the amyl-XA showed obvious adsorption on nylon and polyether sulfone membranes. The five XAs mainly formed [M-H]- parent ions in the ESI- mode and the main daughter ions obtained following collisional fragmentation depended on the alkyl groups of the XAs. Increasing the pH of the ammonia solution in the mobile phase to 11 led to the isomeric separation of n-butyl- and isobutyl-XAs. The optimized mobile phase inhibited the tailing of the chromatographic peak of amyl-XA and effectively improved all the chromatographic peak shapes of XAs. The BEH C18 column was selected as the chromatographic column owing to its better compatibility with high-pH solutions compared with the T3 C18 column. Preservation experiments conducted over 8 d showed that the concentration of all five XAs decreased over time at room temperature; among the XAs analyzed, the concentration of ethyl-XA revealed the most significant decrease. However, the recoveries of the five XAs at 4 and -20 ℃ remained high, ranging from 101% to 105% and from 100% to 106%, respectively, on the 8th day. The preservation observed with a high concentration of XAs was similar to that found with a low concentration. The preservation time was extended to 8 days at pH 11 and 4 ℃ away from the light. No significant matrix effects were observed for the five XA samples in surface water and groundwater, but industrial sewage exerted obvious matrix inhibitory effects on ethyl- and isopropyl-XAs. Owing to the short retention times of ethyl- and isopropyl-XAs, the co-fluxed interferents in the industrial sewage depressed the MS signals. The five XAs showed good linearity in the range of 0.25-100 μg/L, with correlation coefficients greater than 0.9996. The method detection limits were as low as 0.03-0.04 μg/L, and the intra- and inter-day precisions were 1.3%-2.1% and 3.3%-4.1%, respectively. The recoveries obtained under low, medium, and high spiked levels (1.00, 20.0, 80.0 μg/L) were 96.9%-133%, 100%-107%, and 104%-112%, respectively. The corresponding RSDs were 2.1%-3.0%, 0.4%-1.9%, and 0.4%-1.6%, respectively. The optimized method was successfully applied to the analysis of XAs in surface water, groundwater, and industrial sewage. The method could separate and detect various congeners and isomers of XAs without the need for cumbersome pretreatment processes, and its advantages include smaller sample requirements, simpler operation, higher sensitivity, and longer preservation time. The proposed technique presents excellent application potential in XA environmental monitoring and water evaluation, and mineral flotation studies.

A High Kinetic Energy Ion Mobility Spectrometer for Operation at Higher Pressures of up to 60 mbar

High Kinetic Energy Ion Mobility Spectrometers (HiKE-IMS) are usually operated at absolute pressures around 20 mbar in order to reach high reduced electric field strengths of up to 120 Td for influencing reaction kinetics in the reaction region. Such operating points significantly increase the linear range and limit chemical cross sensitivities. Furthermore, HiKE-IMS enables ionization of compounds normally not detectable in ambient pressure IMS, such as benzene, due to additional reaction pathways and fewer clustering reactions. However, operation at higher pressures promises increased sensitivity and smaller instrument size. In this work, we therefore study the theoretical requirements to prevent dielectric breakdown while maintaining high reduced electric field strengths at higher pressures. Furthermore, we experimentally investigate influences of the pressure, discharge currents and applied voltages on the corona ionization source. Based on these results, we present a HiKE-IMS that operates at a pressure of 60 mbar and reduced electric field strengths of up to 105 Td. The corona experiments show shark fin shaped curves for the total charge at the detector with a distinct optimum operating point in the glow discharge region at a corona discharge current of 5 μA. Here, the available charge is maximized while the generation of less-reactive ion species like NOx+ is minimized. With these settings, the reactant ion population, H3O+ and O2+, for ionizing and detecting nonpolar substances like n-hexane is still available even at 60 mbar, achieving a limit of detection of just 5 ppbV for n-hexane.

Detecting Hexafluoroisopropanol Using Soft Chemical Ionization Mass Spectrometry and Analytical Applications to Exhaled Breath

Here we explore the potential use of proton transfer reaction/selective reagent ion-time-of-flight-mass spectrometry (PTR/SRI-ToF-MS) to monitor hexafluoroisopropanol (HFIP) in breath. Investigations of the reagent ions H3O+, NO+, and O2+• are reported using dry (relative humidity (rH) ≈ 0%) and humid (rH ≈ 100%)) nitrogen gas containing traces of HFIP, i.e., divorced from the complex chemical environment of exhaled breath. HFIP shows no observable reaction with H3O+ and NO+, but it does react efficiently with O2+• via dissociative charge transfer resulting in CHF2+, CF3+, C2HF2O+, and C2H2F3O+. A minor competing hydride abstraction channel results in C3HF6O+ + HO2• and, following an elimination of HF, C3F5O+. There are two issues associated with the use of the three dominant product ions of HFIP, CHF2+, CF3+, and C2H2F3O+, to monitor it in breath. One is that CHF2+ and CF3+ also result from the reaction of O2+• with the more abundant sevoflurane. The second is the facile reaction of these product ions with water, which reduces analytical sensitivity to detect HFIP in humid breath. To overcome the first issue, C2H2F3O+ is the ion marker for HFIP. The second issue is surmounted by using a Nafion tube to reduce the breath sample's humidity prior to its introduction into drift tube. The success of this approach is illustrated by comparing the product ion signals either in dry or humid nitrogen gas flows and with or without the use of the Nafion tube, and practically from the analysis of a postoperative exhaled breath sample from a patient volunteer.

Kinetic Role of Reactive Intermediates in Controlling the Formation of Chlorine Dioxide in the Hypochlorous Acid–Chlorite Ion Reaction

An advanced experimental protocol is reported for studying the kinetics and mechanism of the complex redox reaction between chlorite ion and hypochlorous acid under acidic condition. The formation of ClO2 is followed directly by the classical two-component stopped-flow method. In sequential stopped-flow experiments, the target reaction is chemically quenched using NaI solution and the concentration of each reactant and product is monitored as a function of time by utilizing the principles of kinetic discrimination. Thus, in contrast to earlier studies, not only the formation of one of the products but the decay of the reactants was also directly followed. This approach provides a firm basis for postulating a detailed mechanism for the interpretation of the experimental results under a variety of conditions. The intimate details of the reaction are explored by simultaneously fitting 78 kinetic traces, i.e., the concentration vs. time profiles of ClO2-, HOCl, and ClO2, to an 11-step kinetic model. The most important reaction steps were identified, and it was shown that two reactive intermediates have a pivotal role in the mechanism. While chlorate ion predominantly forms via the reaction of Cl2O, chlorine dioxide is exclusively produced in reaction steps involving Cl2O2. This study leads to clear conclusions on how to control the stoichiometry of the reaction and achieve optimum conditions to produce chlorine dioxide and to reduce the formation of the toxic chlorate ion in practical applications.

Preparation, Characterization, Antioxidant and Antibacterial Studies of New Metal (II) Complexes with Schiff Base for 3-amino-1-phenyl-2- pyrazoline-5-one

A new ligand complexes have been synthesis from reaction of metal ions of Mn(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Hg(II), Pd(II) and Pt(II) with schiff base LH. 5-[(2-Hydroxy-naphthalen-1-ylmethylene)-amino]-2-phenyl-2,4-dihydro-pyrazol-3-one, this ligand was characterized by Fourier transform infrared (FTIR), UV-vis, 1H, 13CNMR, and mass spectra. All complexes were characterized by techniques micro analysis C.H.N, UV-vis and FTIR spectral studies, atomic absorption, chloride content, molar conductivity measurements and magnetic susceptibility. The ligand acts as bidentate, coordination through nitrogen atom from azomethin group and deprotonated phenolic oxygen atom. The spectroscopic and analytical measurements showed that the geometric shape of the prepared complexes is octahedral, while the square planar of the palladium and platinum complexes. The ligand and its complexes were having been screened for their antimicrobial activities and antioxidant

Probing radical versus proton migration in the aniline cation with IRMPD spectroscopy

Intramolecular radical and proton migration in the gas phase are important processes driving the dissociation reactions underlying common tandem mass spectrometry processes, such as collision-induced and electron-induced dissociation reactions (CID and ExD). Mechanistic insights in these processes requires experiments that probe the molecular structures of ions along the reaction pathways, usually combined with quantum-chemical calculations. The combination of ion trap mass spectrometry with IR laser spectroscopy, pioneered among others by Dieter Gerlich, provides a particularly effective method to explore details of the ion structures. In this work, we employ infrared multiple-photon dissociation (IRMPD) spectroscopy and density functional theory (DFT) calculations to probe the reactant and product ion structures of a homolytic bond cleavage reaction. First, we employ IRMPD spectroscopy to establish that protonation of the 4-bromoaniline precursor occurs on the amine moiety and then that C-Br homolytic cleavage produces the π-radical cation of aniline. Transition-state calculations are performed to compare the various pathways that connect reactant and product ions, including both proton and radical transfer mechanisms.

Bias-free visible light-driven photoelectrochemical water splitting of type II ZnO/CuS core/shell heterojunction nanotube arrays

Solar-driven water splitting of semiconductor photoelectrodes via photoelectrochemical (PEC) cell has been regarded as the most promising approach to mitigate the energy crisis and environmental issues in the future. In this work, CuS nanoparticles (NPs) are deposited on ZnO nanotube arrays (ZnO/CuS NTAs) via successive ion layer absorption and reaction method for PEC water splitting under visible light irradiation without applying bias. The excellent light harvesting capacity of CuS NPs from visible to near infrared region not only expands the light harvesting of ZnO NTAs into near infrared region, but also substantially boosts light absorption ranging from 300 to 800 nm. Moreover, CuS NPs coupled on ZnO NTAs can establish a type-II band alignment between ZnO and CuS. Consequently, the ZnO/CuS NTAs photoanode exhibits the significantly boosted PEC water splitting performance under visible light illumination (λ > 420 nm) without applying bias. The photocurrent density of the ZnO/CuS NTAs photoanode is 21.2 μA/cm2, which is increased by 9 times compared to that of the pure ZnO NTAs photoanode. The enhancement in PEC water splitting performance for ZnO/CuS NTAs is attributed to (i) the cooperative actions of ZnO and CuS; (ii) significant enhancement in light absorption from the visible to near infrared region achieved by CuS NPs and (iii) efficient charge carrier separation achieved by type-II band alignment.

Effects of Multiple Ion Reactions Based on a CoSe2 /MXene Cathode in Aluminum-Ion Batteries.

Rechargeable aluminum-ion batteries (RAIBs) have emerged as a promising battery storage technology owing to their cost-effectiveness, operational safety, and high energy density. However, their actual capacity is substantially lower than their true capacity and their cycling stability is poor. Therefore, understanding the energy-storage mechanism may contribute to the successful design of a stable electrode material, on which the performance can be optimized. The aim of this study is to investigate AlCl4 - ions in transition metal cathode materials and mechanisms that enable for their high-energy-storage potential and low Coulombic efficiency. Results of theoretical analysis and experimental verification show that a multi-ion transport mechanism is responsible for the electrochemical behavior of the battery. The lattice distortion of CoSe2 caused by AlCl4 - ion intercalation, has a considerable effect on the initial stability of the battery. MXene as a support material reduces the size of CoSe2 growing on its surface, effectively inhibiting the lattice distortion caused by the interaction with the aluminum-anion complex, thus addressing the issues of poor reversibility, cycle instability, and low Coulombic efficiency of the battery. Hence, understanding the impact of MXene on the battery may aid in further improving the design of electrode materials.

Reactions of Nickel Ions in Water Radiolysis up to 300 °C

Radiation chemistry of hydrated metal ions plays a significant role in the field of nuclear energy, especially regarding water radiolysis in coolant water in nuclear reactors. This work reports new experimental data on the reactivity of Ni2+/+ species under critical conditions of temperature and pressure. The reaction rates of hydrated nickel ions with water radiolysis products (e-aq, •OH, H, and H2O2) have been investigated for a 25-300 °C temperature range and 200 bar pressure using electron pulse radiolysis/transient absorption. Extensive experiments with the Ni2+/+ species in various salts and pH up to 300 °C were performed. Kinetic decay traces of short-lived monovalent nickel ions were fitted to extract the rate constants versus temperature up to 300 °C. A blue shift of the absorption spectrum of the monovalent nickel ion with increasing temperature was demonstrated, which may indicate a change in the average coordination number. The Arrhenius parameters for the reactions of Ni2+ with e-aq and Ni+ with •OH, H, and H2O2 were obtained. All measured rate constants increased with temperature and followed Arrhenius behavior.

Qualitative characterization of nitrogen-containing compounds in jet and diesel fuel extracts by using (+) electrospray ionization coupled to a linear quadrupole ion trap/orbitrap mass spectrometer

The development of analytical methods for the characterization of nitrogen-containing compounds (NCCs) in liquid transportation fuels are critical, as these compounds adversely affect fuel storage and thermal stability. In this work, (+) electrospray ionization coupled to a linear quadrupole ion trap/orbitrap mass spectrometer provided detailed chemical analysis of the NCCs in jet and diesel fuels. Upon methanol extractions of the individual fuels (three jet fuels and one diesel), the methanol layer was diluted and injected into the ESI source where protonation was the dominant ionization reaction for the NCCs, which exhibited little to no fragmentation. Kendrick mass defect plots were constructed to facilitate chemical characterization. Many chemical classes of NCCs (i.e., alkylamines, pyridines, indoles, quinolines, carbazoles) were identified in the jet and diesel fuel extracts. Compositional differences were observed when the jet fuel extracts were compared to each other and when compared to the diesel extract. For example, the most abundant NCCs in Jet fuel 1 had empirical formulas of CnH(2n)N (decahydroquinolines/decahydroisoquinolines) and CnH(2n-6)N (indolines/tetrahydroquinolines/tetrahydroisoquinolines). Conversely, the most abundant NCCs in Jet fuel 2 had empirical formulas of CnH(2n-6)N and CnH(2n-10)N (quinolines/isoquinolines/naphthylamines) while the most abundant NCCs in Jet fuel 3 had empirical formulas of CnH(2n+4)N (alkylamines). The ionized NCCs derived from the jet fuels had wider carbon number ranges than compared to those reported in previous studies. The average molecular weights, ring and double bond equivalent values and total carbon numbers for the ionized NCCs in the four extracts ranged from 192.8–215.3 Da, 1.7–5.0 and 13.5–14.8, respectively. Further, the average carbon number for each homologue ion series (ions with the same empirical formula but differ by 14 Da) were determined. Collision-activated dissociation was also investigated to evaluate its efficacy at providing structural elucidation and isomeric differentiation for ionized NCCs. Overall, the high-resolution mass spectrometry measurements provided thorough chemical characterization that may aid in linking NCC compositions to storage and thermal stability failures and advance the current understanding of issues concerning fuel incompatibility upon the mixing of different fuels.

Electrical Modeling and Impedance Spectra of Lithium-Ion Batteries and Supercapacitors

In this study, electrical models for cylindrical/pouch-type lithium Li-ion batteries and supercapacitors were investigated, and the impedance spectra characteristics were studied. Cylindrical Li-ion batteries use Ni, Co, and Al as the main materials, while pouch-type Li-ion batteries use Ni, Co, and Mn as the main materials. Herein, 2600–3600 mAh 18650-type cylindrical Li-ion batteries, 5000 mAh 21700-type cylindrical Li-ion batteries, 37–50.5 Ah pouch-type Li-ion batteries, and a 2.7 V, 600 F supercapacitor are compared and analyzed. For a cylindrical Li-ion battery, the RS value of a battery with a protection device (circular thermal disc cap) is in the range of 14–38 mΩ. For the 18650-type cylindrical Li-ion battery with a protection device, the RS value of the battery is between 48 and 105 mΩ, and the protection device increases the RS value by at least 33 mΩ. A good Li-ion battery exhibits RS. Moreover, it has small overall RP and CP values. For the 21700-type cylindrical Li-ion battery with a protection device, the RS value of the battery is 25 mΩ. For the pouch-type Li-ion battery, the RS value of the battery is between 0.86 and 1.04 mΩ. For the supercapacitor, the RS value of the battery is between 0.4779 and 0.5737 mΩ. A cylindrical Li-ion battery exhibits a semicircular shape in the impedance spectrum, due to the oxidation and reduction reactions of Li ions, and the impedance increases with a slope of 45° in the complex plane, due to the ZW generated by Li ion diffusion. However, for a pouch-type Li-ion battery, the impedance spectrum exhibits a part of the semicircular shape, due to the oxidation and reduction reactions of Li ions, and the ZW generated by Li ion diffusion does not appear. In a supercapacitor, the oxidation and reduction reactions of ions do not appear at all, and the ZW generated by Li ion diffusion does not occur.

Different reactivities of H3 O+ (H2 O)n with unsaturated and saturated aldehydes: ligand-switching reactions govern the quantitative analytical sensitivity of SESI-MS.

The detection sensitivity of secondary electrospray ionisation mass spectrometry (SESI-MS) is much lower for saturated aldehydes than for unsaturated aldehydes. This needs to be understood in terms of gas phase ion-molecule reaction kinetics and energetics to make SESI-MS analytically more quantitative. Parallel SESI-MS and selected ion flow tube mass spectrometry (SIFT-MS) analyses were carried out of air containing variable accurately determined concentrations of saturated (C5, pentanal; C7, heptanal; C8 octanal) and unsaturated (C5, 2-pentenal; C7, 2-heptenal; C8, 2-octenal) aldehyde vapours. The influence of the source gas humidity and the ion transfer capillary temperature, 250 and 300°C, in a commercial SESI-MS instrument was explored. Separate experiments were carried out using SIFT to determine the rate coefficients, k73 , for the ligand-switching reactions of the H3 O+ (H2 O)3 ions with the six aldehydes. The relative slopes of the plots of SESI-MS ion signal against SIFT-MS concentration were interpreted as the relative SESI-MS sensitivities for these six compounds. The sensitivities for the unsaturated aldehydes were 20 to 60 times greater than for the corresponding C5, C7 and C8 saturated aldehydes. Additionally, the SIFT experiments revealed that the measured k73 are three or four times greater for the unsaturated than for the saturated aldehydes. The trends in SESI-MS sensitivities are rationally explained by differences in the rates of the ligand-switching reactions, which are justified by theoretically calculated equilibrium rate constants derived from thermochemical density functional theory (DFT) calculations of Gibb's free energy changes. The humidity of SESI gas thus favours the reverse reactions of the saturated aldehyde analyte ions, effectively suppressing their signals in contrast to their unsaturated counterparts.

High Optical Contrast of Quartet Dual-Band Electrochromic Device for Energy-Efficient Smart Window.

A quartet dual-band electrochromic device (ECD) was developed to selectively control the transmittance from the visible to near-infrared wavelengths for the application of an energy-efficient smart window. The new AgNO3+TBABr+LiClO4 (ATL)-based electrolyte was developed to independently control the redox reaction of lithium and silver ions to demonstrate the quartet mode of an ECD. A dual-band ECD with a sandwich structure was assembled using an ATL-based electrolyte, WO3 electrochromic layer, and antimony-doped tin oxide (ATO) ion storage layer. The employed WO3 and ATO films were fabricated using a nanoparticle deposition system (NPDS), a novel ecofriendly dry deposition method. Four modes, namely, transparent, warm, cool, and all-block modes, were demonstrated via an independent redox reaction of both lithium and silver ions through the simple control of the applied voltage. In the warm mode, the localized surface plasmon resonance effect was exploited by producing silver nanoparticles upon two-step voltage application. Furthermore, since the high surface roughness of the WO3 thin film fabricated by NPDS maximized the light scattering effect, 0% transmittance at all wavelengths was observed in the all-block mode. Dual-band ECD showed high optical contrasts of 73% and long-term durability over 1000 cycles with no degradation. Therefore, the possibility of controlling transmittance at the target wavelength was confirmed using a simple device with a simple process, suggesting a new strategy for the design of dual-band smart windows to reduce the energy consumption of buildings.

Increasing Reaction Rates of Water-Soluble Porphyrins for 64Cu Radiopharmaceutical Labeling.

Searching for new compounds and synthetic routes for medical applications is a great challenge for modern chemistry. Porphyrins, natural macrocycles able to tightly bind metal ions, can serve as complexing and delivering agents in nuclear medicine diagnostic imaging utilizing radioactive nuclides of copper with particular emphasis on 64Cu. This nuclide can, due to multiple decay modes, serve also as a therapeutic agent. As the complexation reaction of porphyrins suffers from relatively poor kinetics, the aim of this study was to optimize the reaction of copper ions with various water-soluble porphyrins in terms of time and chemical conditions, that would meet pharmaceutical requirements and to develop a method that can be applied for various water-soluble porphyrins. In the first method, reactions were conducted in a presence of a reducing agent (ascorbic acid). Optimal conditions, in which the reaction time was 1 min, comprised borate buffer at pH 9 with a 10-fold excess of ascorbic acid over Cu2+. The second approach involved a microwave-assisted synthesis at 140 °C for 1-2 min. The proposed method with ascorbic acid was applied for radiolabeling of porphyrin with 64Cu. The complex was then subjected to a purification procedure and the final product was identified using high-performance liquid chromatography with radiometric detection.