Transfer Distance Research Articles

Wireless Power Transfer of Electric Vehicle Battery Charging

Abstract: Wireless power transfer (WPT) is a cutting-edge technology that utilizes magnetic resonance to eliminate the need for cumbersome wires. WPT builds upon the principles of inductive power transfer and has been rapidly advancing in recent years. At power levels of kilowatts, the transfer distance can range from a few millimeters to several hundred meters, achieving an efficiency of over 90%. This progress has made WPT an attractive option for electric vehicle (EV) charging, both in stationary and dynamic settings. This study examines the latest developments in WPT as it pertains to wireless charging for EVs. By integrating WPT into EVs, challenges such as charging time, range, and cost can be effectively addressed. Battery technology is no longer a limiting factor in widespread adoption, and it is hoped that researchers will be inspired by recent advancements to further enhance WPT and expand the use of EVs.

AgCo bimetallic cocatalyst modified g-C3N4 for improving photocatalytic hydrogen evolution

Bimetallic AgCo/g-C3N4 photocatalysts were successfully prepared by a facile chemical reduction method and used to investigate their photocatalytic H2 production performance. Bimetallic AgCo as a cocatalyst can be well matched with g-C3N4, which is beneficial for increasing the number of active reaction sites and narrowing the band gap. A possible photocatalytic mechanism was explored by XRD, FTIR, SEM, TEM, UV–vis DRS, BET, and PL characterization. The photocatalytic H2 production activity of the optimal 5%AgCo/g-C3N4 photocatalyst reached 12994.2 μmoL/g, which was 54.7 times higher than g-C3N4. Owing to the close interfacial contact between bimetallic AgCo and g-C3N4, the transfer distance was shortened, and the photogenerated electron and hole pairs were effectively separated. This study provides a new strategy for the synthesis of excellent H2 production photocatalysts using bimetallic nanoparticles.

Tuning and high temperature fluorescence properties of LaPO4:Sm3+ nanophosphors

A series of LaPO4:x%Sm3+ nanophosphors were successfully synthesized through a one-step hydrothermal method, where the acidity of the reaction system was meticulously modulated without the addition of any organic compounds. The influence of pH values and Sm3+ doping concentration on the structure, morphology, and luminescent properties of LaPO4:x%Sm3+ was systematically investigated. The composition, structure, morphology, and luminescent properties of the products were characterized and analyzed using advanced techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM, EDS), transmission electron microscopy (TEM), and fluorescence spectrophotometry (FL). The results indicate that the acidity of the reaction system effectively influences the morphology and size of the nanophosphors, facilitating the controlled synthesis of nanorod-shaped, nano-spherical, and ellipsoidal phosphors. When the Sm3+ doping concentration is 2 %, the phosphors exhibit maximum luminescent intensity and fluorescence lifetime. The energy transfer between Sm3+ ions in LaPO4:x%Sm3+ is identified as electric dipole-electric dipole interaction, with a critical distance for energy transfer established at 1.593 nm. LaPO4:2%Sm3+ exhibits good thermal stability, characterized by a thermal quenching activation energy of 0.1660 eV. The main outcome of this research, LaPO4:2%Sm3+ phosphor, exhibits significant potential for use in optical sensors, as well as promising applications in solar cells and biological fields.

Enhanced H2 Generation via Piezoelectric Reforming of Waste Sugars and Fruits Using Au-Decorated g-C3N4

The food industry is responsible for generating considerable amounts of waste, such as excess fruits and leftover sugars, which contribute to resource depletion and pose environmental challenges. This research delves into the application of gold-modified graphitic carbon nitride nanosheets (Au/CN) as a potent catalyst for the transformation of these food wastes into H2 via piezoelectric reforming during sonication. Au/CN demonstrated a superior rate of H2 evolution compared to pristine g-C3N4 (i.e., 1533.3 vs. 364.9 µmol/g/h) and it maintained its efficiency through multiple cycles of use. The catalytic activity was found to be optimal at a neutral pH level and with increased sugar concentrations. The enhanced catalytic performance of Au/CN was ascribed to the efficient segregation of charge carriers as well as the reduced charge transfer distance. This study underscores the viability of using Au/CN as a means for converting food wastes into a sustainable source of H2 energy.

Upconversion-based hydrogel kit with Python-assisted analysis platform for sample-to-result detection of organophosphorus pesticide

On-site quantitative analysis of pesticide residues is crucial for monitoring environmental quality and ensuring food safety. Herein, we have developed a reliable hydrogel portable kit using NaYbF4@NaYF4: Yb, Tm upconversion nanoparticles (UCNPs) combined with MnO2 nanoflakes. This portable kit is integrated with a smartphone reader and Python-assisted analysis platform to enable sample-to-result analysis for chlorpyrifos. The novel UCNPs maximizes energy donation to MnO2 acceptor by employing 100 % of activator Yb3+ in the nucleus for NIR excitation energy collection and confining emitter Tm3+ to the surface layer to shorten energy transfer distance. Under NIR excitation, efficient quenching of upconversion blue-violet emission by MnO2 nanoflakes occurs, and the quenched emission is recovered with acetylcholinesterase-mediated reactions. This process allows for the determination of chlorpyrifos by inhibiting enzymatic activity. The UCNPs/MnO2 were embedded to fabricate a hydrogel portable kit, the blue-violet emission images captured by smartphone were converted into corresponding gray values by Python-assisted superiority chart algorithm which achieves a real-time rapid quantitative analysis of chlorpyrifos with a detection limit of 0.17 ng mL−1. At the same time, pseudo-color images were also added by Python in “one run” to distinguish images clearly. This sensor detection with Python-assisted analysis platform provides a new perspective on pesticide monitoring and broadens the application prospects in bioanalysis.

Machine learning aided understanding and manipulating thermal transport in amorphous networks

Thermal transport plays a pivotal role across diverse disciplines, yet the intricate relationship between amorphous network structures and thermal conductance properties remains elusive due to the absence of a reliable and comprehensive network’s dataset to be investigated. In this study, we have created a dataset comprising multiple amorphous network structures of varying sizes, generated through a combination of the node disturbance method and Delaunay triangulation, to fine-tune an initially random network toward both increased and decreased thermal conductance C. The tuning process is guided by the simulated annealing algorithm. Our findings unveil that C is inversely dependent on the normalized average shortest distance Lnorm connecting heat source nodes and sink nodes, which is determined by the network topological structure. Intuitively, the amorphous network with increased C is associated with an increased number of bonds oriented along the thermal transport direction, which shortens the heat transfer distance from the source to sink node. Conversely, thermal transport encounters impedance with an augmented number of bonds oriented perpendicular to the thermal transport direction, which is demonstrated by the increased Lnorm. This relationship can be described by a power law C=Lnormα, applicable to the diverse-sized amorphous networks we have investigated.

Redox Properties of Bacillus subtilis Ferredoxin:NADP+ Oxidoreductase: Potentiometric Characteristics and Reactions with Pro-Oxidant Xenobiotics.

Bacillus subtilis ferredoxin:NADP+ oxidoreductase (BsFNR) is a thioredoxin reductase-type FNR whose redox properties and reactivity with nonphysiological electron acceptors have been scarcely characterized. On the basis of redox reactions with 3-acetylpyridine adenine dinucleotide phosphate, the two-electron reduction midpoint potential of the flavin adenine dinucleotide (FAD) cofactor was estimated to be -0.240 V. Photoreduction using 5-deazaflavin mononucleotide (5-deazaFMN) as a photosensitizer revealed that the difference in the redox potentials between the first and second single-electron transfer steps was 0.024 V. We examined the mechanisms of the reduction of several different groups of non-physiological electron acceptors catalyzed by BsFNR. The reactivity of quinones and aromatic N-oxides toward BsFNR increased when increasing their single-electron reduction midpoint redox potentials. The reactivity of nitroaromatic compounds was lower due to their lower electron self-exchange rate, but it exhibited the same trend. A mixed single- and two-electron reduction reaction was characteristic of quinones, whereas reactions involving nitroaromatics proceeded exclusively via the one-electron reduction reaction. The oxidation of FADH• to FAD is the rate-limiting step during the oxidation of fully reduced FAD. The calculated electron transfer distances in the reaction with nitroaromatics were close to those of other FNRs including the plant-type enzymes, thus demonstrating their similar active site accessibility to low-molecular-weight oxidants despite the fundamental differences in their structures.

Thermal shock triggers microexplosion combustion in graded fuel and oxidizer encapsulation microspheres with improved combustion efficiency

The combustion agglomeration of aluminum (Al) and the long heat and mass transfer distance between Al and oxidizer cause serious two-phase flow loss and slag accumulation in the engine of solid propellants. Here, we present an effective strategy by in-situ encapsulating graded nano-aluminum (nAl) and micron-aluminum (μAl) in ammonium perchlorate (AP) simultaneously by using hydroxymethyl cellulose (HMC) as adhesive and constructing a compact coupling fuel oxidizer complex high-energy microsphere (μAl/nAl@AP/HMC) to enhance the energy release efficiency and combustion efficiency. Compared with physical mixture (PM), the ignition delay time and combustion time of μAl/nAl@AP/HMC microspheres are reduced by 69.58 % and 69.87 %, owing to the decomposition process control of AP through the adsorption and spatial constraint effect on the interface between metal fuels and oxidizer. Furthermore, the nAl embedded in the AP surface forms a hot spot around the μAl to promote the combustion reaction, thereby shortening the cavitation threshold and tensile limit time of μAl and accelerating the occurrence of microexplosion. Microexplosion effect in μAl/nAl@AP/HMC microsphere significantly weakens combustion agglomeration and improves combustion efficiency and energy release efficiency by sharp shrinkage of combustion condensation products, which addresses the challenges on energy output and combustion efficiency in high-density solid propellants.

QM/MM Free Energy Calculations of Long-Range Biological Protonation Dynamics by Adaptive and Focused Sampling.

Water-mediated proton transfer reactions are central for catalytic processes in a wide range of biochemical systems, ranging from biological energy conversion to chemical transformations in the metabolism. Yet, the accurate computational treatment of such complex biochemical reactions is highly challenging and requires the application of multiscale methods, in particular hybrid quantum/classical (QM/MM) approaches combined with free energy simulations. Here, we combine the unique exploration power of new advanced sampling methods with density functional theory (DFT)-based QM/MM free energy methods for multiscale simulations of long-range protonation dynamics in biological systems. In this regard, we show that combining multiple walkers/well-tempered metadynamics with an extended system adaptive biasing force method (MWE) provides a powerful approach for exploration of water-mediated proton transfer reactions in complex biochemical systems. We compare and combine the MWE method also with QM/MM umbrella sampling and explore the sampling of the free energy landscape with both geometric (linear combination of proton transfer distances) and physical (center of excess charge) reaction coordinates and show how these affect the convergence of the potential of mean force (PMF) and the activation free energy. We find that the QM/MM-MWE method can efficiently explore both direct and water-mediated proton transfer pathways together with forward and reverse hole transfer mechanisms in the highly complex proton channel of respiratory Complex I, while the QM/MM-US approach shows a systematic convergence of selected long-range proton transfer pathways. In this regard, we show that the PMF along multiple proton transfer pathways is recovered by combining the strengths of both approaches in a QM/MM-MWE/focused US (FUS) scheme and reveals new mechanistic insight into the proton transfer principles of Complex I. Our findings provide a promising basis for the quantitative multiscale simulations of long-range proton transfer reactions in biological systems.

Adsorption and sensing characteristics of insulating gas C4F7N on 3d late transition metal‐phthalocyanine: Theoretical and experimental study

AbstractHeptafluoroisobutyronitrile (C4F7N) is being considered as a promising alternative to the greenhouse gas SF6 in the electrical industry. However, its biotoxicity necessitates the development of gas sensing technology to detect leaked C4F7N. A combination of density functional theory and experiments was employed to evaluate the adsorption and sensing performance of different metal‐phthalocyanines as potential sensing materials for C4F7N detection. The study included exploring adsorption configurations with adsorption energies, electron transfer, and adsorption distance, as well as comparisons of electronic properties, electron distribution, and density of states (DOS) among the MPcs. Furthermore, gas sensing experiments were conducted using different MPcs to detect 25–100 ppm C4F7N. The results revealed that Mn‐Pc, Fe‐Pc, Co‐Pc, and Zn‐Pc exhibited considerable chemical interactions, while Ni‐Pc and Cu‐Pc showed weaker adsorption strength. These findings were further elucidated based on the electron density and DOS of atomic orbitals. Moreover, gas sensing experiments indicated that Co‐Pc demonstrated a higher response compared to Fe‐Pc at the same concentration of C4F7N. Overall, the theoretical and experimental insights offer valuable guidance for C4F7N detection and provide a systematic approach to screen and explore organometallic polymer‐based gas sensors applicable in various fields.

Enhanced charge separation of Cu-BTC@CuSe@TiO2 hollow octahedrons for efficient CO2 photoreduction with superior CO selectivity

Solar-driven photocatalytic conversion of CO2 into high-value-added fuels has attracted widespread attention. However, the relatively low conversion efficiency and product yield severely limited photocatalytic applications. In this work, binary Cu-BTC@TiO2 catalysts with adjustable inner cavity were prepared using copper-based metal organic framework (Cu-BTC) octahedrons as substrate via a solvothermal reaction. In this process, the inner Cu-BTC octahedrons can be controllably etched into a hollow octahedral structure in the presence of HF. Subsequently, the Cu-BTC@CuSe@TiO2 hollow octahedrons (HOs) were fabricated by selenization reaction and exhibited various properties such as abundant active sites for CO2 adsorption and reduction reactions, shortened charge transfer distance to prevent electron-hole recombination, and internal reflection/scattering effects to improve solar light utilization. Moreover, the formed dual p-n heterostructures between p-type CuSe and n-type semiconductors (Cu-BTC and TiO2) effectively promote spatial separation and migration of charge carriers. The synergistic effect of these advantages makes the optimized Cu-BTC@CuSe@TiO2 HO catalyst exhibit remarkable CO2 photoreduction performance with a CO production rate of 72.3 μmol h−1 g−1 and near 100 % selectivity. This work opens a new pathway for designing highly active photocatalysts with excellent product selectivity.

Orbital-Optimized Versus Time-Dependent Density Functional Calculations of Intramolecular Charge Transfer Excited States.

The performance of time-independent, orbital-optimized calculations of excited states is assessed with respect to charge transfer excitations in organic molecules in comparison to the linear-response time-dependent density functional theory (TD-DFT) approach. A direct optimization method to converge on saddle points of the electronic energy surface is used to carry out calculations with the local density approximation (LDA) and the generalized gradient approximation (GGA) functionals PBE and BLYP for a set of 27 excitations in 15 molecules. The time-independent approach is fully variational and provides a relaxed excited state electron density from which the extent of charge transfer is quantified. The TD-DFT calculations are generally found to provide larger charge transfer distances compared to the orbital-optimized calculations, even when including orbital relaxation effects with the Z-vector method. While the error on the excitation energy relative to theoretical best estimates is found to increase with the extent of charge transfer up to ca. -2 eV for TD-DFT, no correlation is observed for the orbital-optimized approach. The orbital-optimized calculations with the LDA and the GGA functionals provide a mean absolute error of ∼0.7 eV, outperforming TD-DFT with both local and global hybrid functionals for excitations with a long-range charge transfer character. Orbital-optimized calculations with the global hybrid functional B3LYP and the range-separated hybrid functional CAM-B3LYP on a selection of states with short- and long-range charge transfer indicate that inclusion of exact exchange has a small effect on the charge transfer distance, while it significantly improves the excitation energy, with the best-performing functional CAM-B3LYP providing an absolute error typically around 0.15 eV.

The ball's in your court: Trends, causes, outcomes, and costs of patient transfer for pediatric testicular torsion

BackgroundThe transfer of pediatric patients with testicular torsion from community hospitals to pediatric centers can be a time and resource-intensive step toward emergent surgical intervention. ObjectiveWe sought to describe trends of patient transfer in our state and compare clinical outcomes and health system costs between patients transferred and treated primarily at a pediatric center. Study DesignThis retrospective cohort study compared patients aged 1-18 years who presented directly to a pediatric center to those transferred for acute testicular torsion from 2018-2023. Exclusion criteria included age <1 year, non-urgent surgery, and admission from clinic. Patient age, BMI, Tanner stage, ASA class, insurance coverage, and presentation time were covariates. Group characteristics and times from symptom onset to initial ED presentation to surgery were compared via two-sided Student’s t-tests. Clinical outcomes (orchiectomy, testicular atrophy) were compared via Fisher’s exact tests. Costs from transferring hospitals were estimated from costs at our institution, and medical transport costs were extrapolated from contract prices between transport agencies and the pediatric center to compare total episode-of-care cost. ResultsA total of 133 cases (37 primaries, 96 transfers) met inclusion criteria. Transfers increased over the study period (67% to 75%). There were no significant differences in age, Tanner stage, ASA score, BMI, or time of day of presentation between groups. Median transfer distance was 12 miles (IQR 7-22) and time was 1 hour (IQR 1-2). More than half of cases (53%) were transferred due to hospital policy regarding surgical treatment of minors, and 25% due to lack of urology coverage. Time from initial ED site to OR was nearly doubled for the transfer group (median 4.5 vs 2.5 hours, p=0.02). Despite a higher rate of orchiectomy in the primary group (43 vs 22%, p=0.01), this difference was not significant after stratification by symptom duration. The estimated average cost of care for patients transferred was twice that of primary patients ($15,082 vs $6,898). DiscussionTransfer of pediatric patients in our state for testicular torsion has increased in recent years. Hospital policies and local urology coverage are primary drivers of patient transfer which nearly doubled time to surgical intervention and more than doubled cost of care. Clinical outcomes were driven by delayed presentation. ConclusionTransfer of pediatric patients for testicular torsion nearly doubles time to surgical intervention and more than doubles cost of care. Restrictive hospital policies and gaps in rural hospital urology coverage present opportunities to improve the quality and efficiency of care for these children.

EVALUASI AKTIVITAS NON VALUE ADDED DENGAN MENGGUNAKAN METODE VALUE STREAM MAPPING DAN PROCESS ACTIVITY MAPPING

Samsul Blacksmith is a blacksmith who produces palm harvesting tools (dodos), in the production process there is still waste which causes the daily production target not to be achieved, this study aims to determine the root causes of waste and provide alternative improvements. This research was conducted with 4 stages, first mapping all production activities using value stream mapping (VSM), the second stage identifying waste using the Process activity mapping (PAM) method, the third stage identifying the root causes of waste using the 5 whys method, the last stage providing alternative improvements to reduce or eliminate waste. The results showed that waste occurred due to the absence of workpiece transfer tools and long transfer distances, simple furnaces without the use of heat shields, and inefficient workbenches, the proposed alternative re-layout of the production floor, designing furnaces, and designing work areas, was able to reduce the lead time of the production process from 6.260 seconds to 4.907,8 seconds (improvement with MOST and MTM), and increased the PCE value from 51.6% to 65.8%.

Evaluation of movability of shale oil in organic matter in depletion production by REV-scale simulations

The oil transfer in shale oil formations includes the oil flow in inorganic and organic pores, and the diffusion in the organic matter (OM). A novel triple-continuum model (OM matrix, organic pores, inorganic matrix) is proposed coupling the oil flow (in organic and inorganic pores) and diffusion (in OM matrix). The proposed model is further validated by three-dimensional (3D) numerical simulations. The simulation results show that the proportion of oil production of the absorbed oil from OM matrix in the total shale oil production is small due to the relatively slow diffusion process. However, the diffusion of oil from OM matrix to the organic pores can provide extra energy for the oil expansion in inorganic pores, and thus can greatly increase the oil production in the depletion process. The high OM content can prolong the timespan of oil production. More absorbed oil in OM provides more elastic energy for oil depletion in organic and inorganic pores, and thus leads to higher flow rate in the late period of shale oil production. Smaller size of OM means shorter distance for oil transfer from OM to inorganic matrix, and thus accounts for higher movability of oil in OM.

Bismuth-Doped Carbon Dots Decorated Escherichia coli for Enhanced Hydrogen Production.

Photosynthetic inorganic biohybrid systems (PBSs) combining an inorganic photosensitizer with intact living cells provide an innovative view for solar hydrogen production. However, typical whole-cell biohybrid systems often suffer from sluggish electron transfer kinetics during transmembrane diffusion, which severely limits the efficiency of solar hydrogen production. Here, a unique biohybrid system with a quantum yield of 8.42% was constructed by feeding bismuth-doped carbon dots (Bi@CDS) to Escherichia coli (E.coli). In this biohybrid system, Bi@CDS can enter the cells and transfer the electrons upon light irradiation, greatly reducing the energy loss and shortening the distance of electron transfer. More importantly, the photocatalytic hydrogen production of the E.coli-Bi@CDs biohybrid system reached up to 0.95 mmol within 3 h under light irradiation (420-780 nm, 2000 W m-2), which is 1.36 and 2.38 times higher than that in the E.coli-CDs biohybrid system and the E.coli system, respectively. In addition, the mechanism of enhanced hydrogen production was further explored. It was found that the accelerated decomposition of glucose, the accelerated production of pyruvate, the inhibition of lactic acid, and the increase of formic acid were the reasons for the increase of hydrogen production. This work provides a novel strategy for improving the hydrogen production in photosynthetic inorganic biohybrid systems.

Hybrid electromagnetic Halbach array for wireless power transfer (WPT) system using variable and uniform pitch coils

AbstractThe electromagnetic Halbach array (EHA) for wireless power transfer (WPT), designed to improve the transferred power and power transfer distance, has been proven to be effective and can be applied in various consumer applications. This paper presents a hybrid form of the EHA, aimed at improving the quality of power generated and transmitted. The expression for the determination of the magnetic field of a variable pitch flat coil for wireless power transfer and other uses has been derived. The average magnetic field, magnetic flux, and power transfer efficiency are investigated. The power transfer efficiency and the average magnetic field generated by four different design considerations were compared. The hybrid electromagnetic Halbach array wireless power transfer system (HEHA‐WPTS) has also been studied and results are compared with the conventional arrangements. Simulations and experiments were carried out to verify the analytical results obtained. According to the results obtained, the HEHA‐WPTS, with a base coil with variable pitches and uniform side coils, produces a more uniform average magnetic field and a better average power transfer efficiency over a longer power transfer distance.

Impact of Diimine Ligand on Singlet-to-Triplet Charge Transfer Electroabsorption in Iron and Ruthenium Complexes.

The electroabsorption and absorption spectra of eight homoleptic complexes of the general form [M(LL)3]2+ where M = Ru, Fe, and LL = 1,10-phenanthroline (phen), 2,2'-bipyridine (bpy), and 4,4',-(R)2-bpy where R = -OCH3, -CF3, were quantified at 77 K in a butyronitrile glass. Intense metal-to-ligand charge transfer (MLCT) absorption bands were evident in the visible region. Electroabsorption spectra measured with applied electric fields >0.2 MV/cm were analyzed by the two-state Liptay model. Significant light-induced dipole moment changes of = 4-13 D were found consistent with a metal-to-ligand charge transfer (MLCT) excited state comprised an electron localized on a single diimine ligand, [MIII(LL-)(LL)2]*2+, in the initially formed Franck-Condon excited state. A low energy feature evident in the electroabsorption spectra was assigned to a direct singlet-to-triplet MLCT excited state. The identity of the diimine ligand had an unexpected and large impact on these transitions. Analysis relative to the higher energy absorption provides a comparison of spin-allowed and disallowed transitions for first- and second-row transition metal complexes. With the notable exception of [Fe(CF3bpy)3]2+, the change in dipole moment for the 3MLCT excited states was less than or equal to that of the 1MLCT excited states. The charge transfer distances for the iron complexes were generally larger than those for the Ru complexes, a behavior attributed to a smaller degree of iron-diimine coupling in the ground state. A striking result was the sensitivity of the extinction coefficient and spectral profile of the low energy electroabsorption assigned to the identity of the diimine ligand; data that suggests electronic coupling with ligand localized triplet states and high spin metal centered states must be considered when modeling the Franck-Condon excited state.

Magnetic MOFs with flexibility for efficient magnetic-induced swing adsorption

Magnetic-induced swing adsorption is effective because of its easy operation, fast heat generation, and short distance of heat transfer. The energy efficiency of this adsorption method depends on the performance of magnetic adsorbents in alternative magnetic fields. In this work, we fabricated flexible MOF-based magnetic adsorbents and applied them in the magnetic-induced swing adsorption. When magnetic field is turned off, the adsorbents show open pores for C3H8 uptake at room temperature. When magnetic field is turned on, C3H8 is released because magnetic-induced heating drives the adsorbents loss their activity through conformational change of pores derived from aromatic rings tilting and rotation. The flexibility of the adsorbents decreases energy consumption to achieve desorption, which promote the energy efficiency of magnetic-induced swing adsorption. The optimal working capacity can reach 16.8 cm3 g−1, which is superior to various typical adsorbents such as F30/470 (9.32 cm3 g−1), MIL-91(Al) (3.36 cm3 g−1), and SSZ-13 zeolite (4.48 cm3 g−1). This work may open up a new avenue to address the issues caused by high energy consumption and slow heat transfer during desorption.

In-situ targeted removal of naphthalene from groundwater by peroxymonosulfate activation using molecularly imprinted activated carbon: Efficacy, mechanism and applicability

Efficient removal of low-concentration refractory polycyclic aromatic hydrocarbons (PAHs) pollutants is crucial for ensuring groundwater safety. In this study, surface molecularly imprinted catalyst (MIP@AC) was developed based on activated carbon (AC) and molecular imprinting technology, and then MIP@AC was introduced into the simulated permeable reaction barrier to evaluate the performance of MIP@AC activated peroxymonosulfate (PMS) in in-situ targeted remediation of naphthalene (NAP) contaminated groundwater. The results showed that the relative adsorption selectivity coefficient and relative degradation selectivity coefficient of the MIP@AC material relative to the non-imprinted material AC was as high as 31.47 and 10.88, respectively; that is, MIP@AC can better resist the interference of competitive pollutants and achieve efficient targeted removal of NAP. Additionally, the reactive oxygen species (ROS) yield was higher in the MIP@AC/PMS system compared to the AC/PMS system. The target pollutant NAP was precisely enriched in the imprinted cavity of the MIP@AC, realizing that ROS production and pollutant degradation occurred simultaneously in the MIP@AC imprinted cavity. Therefore, the spatial confinement effect of the imprinted cavity shortened the mass transfer distance between the ROS and NAP, thereby reducing the loss of ROS due to self-quenching. Besides, Cl- significantly promoted the targeted removal of NAP, while HCO3- had a slight inhibitory effect; humic acid had no effect because of its larger molecular structure, which does not fit into the small imprinted cavities preferred by NAP. Importantly, the MIP@AC/PMS system demonstrated effective anti-complex matrix interference ability and targeted removal performance for NAP under natural groundwater conditions. This study can promote further research on the surface molecularly imprinted catalyst/PMS system as a new strategy for in-situ targeted remediation technology of contaminated groundwater.