Polar Molecules Research Articles

Biotransformation of Xanthohumol by Entomopathogenic Filamentous Fungi.

Xanthohumol (1) is a major prenylated flavonoid in hops (Humulus lupulus L.) which exhibits a broad spectrum of health-promoting and therapeutic activities, including anti-inflammatory, antioxidant, antimicrobial, and anticancer effects. However, due to its lipophilic nature, it is poorly soluble in water and barely absorbed from the gastrointestinal tract, which greatly limits its therapeutic potential. One method of increasing the solubility of active compounds is their conjugation to polar molecules, such as sugars. Sugar moiety introduced into the flavonoid molecule significantly increases polarity, which results in better water solubility and often leads to greater bioavailability. Entomopathogenic fungi are well known for their ability to catalyze O-glycosylation reactions. Therefore, we investigated the ability of selected entomopathogenic filamentous fungi to biotransform xanthohumol (1). As a result of the experiments, one aglycone (2) and five glycosides (3-7) were obtained. The obtained (2″E)-4″-hydroxyxanthohumol 4'-O-β-D-(4‴-O-methyl)-glucopyranoside (5) has never been described in the literature so far. Interestingly, in addition to the expected glycosylation reactions, the tested fungi also catalyzed chalcone-flavanone cyclization reactions, which demonstrates chalcone isomerase-like activity, an enzyme typically found in plants. All these findings undoubtedly indicate that entomopathogenic filamentous fungi are still an underexploited pool of novel enzymes.

Nutmeg and SPICE: Models and Data for Biomolecular Machine Learning.

We describe version 2 of the SPICE data set, a collection of quantum chemistry calculations for training machine learning potentials. It expands on the original data set by adding much more sampling of chemical space and more data on noncovalent interactions. We train a set of potential energy functions called Nutmeg on it. They are based on the TensorNet architecture. They use a novel mechanism to improve performance on charged and polar molecules, injecting precomputed partial charges into the model to provide a reference for the large-scale charge distribution. Evaluation of the new models shows that they do an excellent job of reproducing energy differences between conformations even on highly charged molecules or ones that are significantly larger than the molecules in the training set. They also produce stable molecular dynamics trajectories and are fast enough to be useful for routine simulation of small molecules.

Molecular dynamics study of shale oil adsorption and diffusion behavior in reservoir nanopores: Impact of hydrocarbon composition and surface type

Understanding shale oil adsorption in reservoir nanopores is essential for efficient extraction. This study used MD simulations to analyze the adsorption and diffusion of two- and multi-component hydrocarbons (Aromatics, Alkanes, Resin) on various shale surfaces (Calcite, Montmorillonite, Quartzite, Organic) at 353 K and 25 MPa. Hydrocarbons formed a bilayer adsorption structure comprising a high-concentration adsorption layer (L1, 0.35–0.90 g/cm3) and a low concentration weak adsorption layer (L2), with adsorption density ranked as Resin > Aromatics > Alkanes. Reservoir surfaces were classified as ionic (e.g., calcite, montmorillonite) and non-ionic (e.g., quartz, graphite), and polar hydrocarbons exhibited higher adsorption densities and energies on ionic surfaces due to combined electrostatic and van der Waals interactions, while non-ionic surfaces showed smaller adsorption differences. For multicomponent hydrocarbons, adsorption layer densities followed the order: graphite > MMT-SiO > quartz > calcite > MMT-Na, with competitive adsorption observed. The polar component exhibited a greater adsorption advantage on the calcite, MMT-SiO side and graphite surfaces due to electrostatic interactions and π-π interactions, and a lesser advantage on the MMT-Na side and quartz surfaces. Hydrocarbon diffusivity was influenced by molecular mass and polarity and ordered as Alkanes > Aromatics ≫ Resin. Polar molecules had a weaker diffusion than nonpolar molecules at similar molecular masses. Among the multicomponent hydrocarbons, the self-diffusion coefficient (Self-D) of Resin increased, while that of lighter components decreased compared to two-component systems. These findings offer strategies for improving shale oil recovery by tailoring injection fluids to reservoir types, anionic surfactants or chelating agents may be used to reduce electrostatic interactions in carbonate and clay reservoirs, while nonionic surfactants may be more effective in quartz reservoirs.

Rotational properties of two interacting cold polar molecules: Linear, symmetric, and asymmetric tops

We examine the potential-energy curves and polarization of the dipole moments of two static polar molecules under the influence of an external dc electric field and their anisotropic dipole-dipole interaction. We model the molecules as quantum rigid rotors to take their rotational degrees of freedom into account and consider a selection of linear, symmetric, and asymmetric top molecules. We provide a comprehensive examination of the energy curves and polarization of the dipoles for varying intermolecular separation and direction of the electric field and find that the properties of the molecules depend strongly on the field's direction at short separations, showing the importance of accounting for molecular rotation. The latter provides insight into the possible effects of accounting for rotational degrees of freedom in molecular dipolar gases. Published by the American Physical Society 2024

Technology Progress in High-Frequency Electromagnetic In Situ Thermal Recovery of Heavy Oil and Its Prospects in Low-Carbon Situations

Heavy oil resources are abundant globally, holding immense development potential. However, conventional thermal recovery methods such as steam injection are plagued by high heat loss, substantial carbon emissions, and significant water consumption, making them incompatible with carbon reduction goals and the sustainable socioeconomic development demands. A new method of high-frequency electromagnetic in situ heating, which targets polar molecules, can convert electromagnetic energy into heat so as to achieve rapid volumetric heating of the reservoir. This method has the potential to overcome the drawbacks of traditional techniques. Nevertheless, it faces significant drawbacks such as limited heating range and inadequate energy supply during later production stages, which necessitates auxiliary enhancement measures. Various enhancement measures have been reported, including nitrogen injection, hydrocarbon solvent injection, or the use of nano-metal oxide injections. These methods are hindered by issues such as pure nitrogen being easy to breakthrough, high costs, and metal pollution. Through extensive literature review, this article charts the evolution of high-frequency electromagnetic in situ heating technology for heavy oil and the current understanding of the coupled heat and mass transfer mechanisms underlying this technology. Moreover, based on a profound analysis of the technology’s progression trends, this work introduces a new direction: CO2-N2 co-injection as an enhancement strategy for high-frequency electromagnetic in situ heavy oil recovery. There is promising potential for the development of new technologies in the future that combine high efficiency, low carbon emissions, environmental friendliness, economic viability, and energy conservation. Furthermore, some research prospects in low-carbon situations and challenges for the new technology in future are presented in detail. All in all, the contribution of the paper lies in the summarizing of some main drawbacks of current enhanced electromagnetic in situ thermal recovery methods, and presents a novel research direction of using CO2-N2 co-injection as an enhancement strategy based on its current research status in low-carbon situations.

Evaluation of compatibility in bio-oil and zinc oxide modified asphalt to facilitate waste recycling

The promotion of bio-oil (Bo) waste in road asphalt modification has significant potential for application and environmental benefits. The thermal storage stability, rheological properties, and nano-microstructural characteristics of the composite modified asphalt system were investigated. The Cole-Cole diagram effectively evaluated the compatibility of modified asphalt, demonstrating high sensitivity and accuracy. Significant interaction energy was observed between zinc oxide (ZnO) and asphaltene, with asphaltene primarily acting as an electron donor during its interaction with ZnO. The three organic small molecules in Bo primarily interacted with the polar molecules in asphalt through ester groups, exhibiting varied interaction effects with asphaltene. Bo influenced the colloidal structure of asphalt mainly through diffusion and molecular intercalation. When Bo constituted 4% of the composite modified asphalt system, the organic small molecules from Bo fully diffused within the asphalt matrix, inhibiting the stacking of aromatic rings in the asphaltene structure and enhancing the aromatic activity of asphaltene. Bo improved the compatibility between ZnO and asphalt primarily through dilution and balancing effects from the perspective of asphaltene components. The research results can promote the promotion and application of bio-oil waste in asphalt pavement engineering, which is an important measure to practice sustainable development.

Rare-Earth Metal Complexes Bearing Electrophilic Carbon and Strongly Polarized Metallacyclopropane Moiety: Synthesis and Diverse Reactivity toward Small Molecules.

Metallacyclopropanes are highly strained and very reactive organometallics; the rare-earth metal complexes bearing both highly reactive electrophilic carbon and strongly polarized metallacyclopropanes are extremely rare. This type of rare-earth metal complexes (κ2-L)RE(η2-C2B10H10)·(THF)3 [L = 1-(2-N-C5H10NCH2CH2)-3-(2,6-iPr2C6H3N═CH)-C8H4N, RE = Lu(1a), Yb(1b), Er(1c), Y(1d), Dy(1e)] bearing the indol-2-yl electrophilic carbon and carboryne-based strongly polarized metallacyclopropanes have been synthesized. Structures of complexes 1 are further confirmed by single-crystal X-ray diffraction and DFT theoretical calculations. It is found that complexes 1 have remarkable reactivity toward different polar unsaturated small molecules, elemental sulfur, and selenium to provide different products (2-15) through the selective reactions of the RE-Ccage, and RE-C2-ind bonds with the given small molecules, respectively. The reactivities of these complexes are different from those of the reported rare-earth metallacyclopropenes and d-block metal-carborynes.

High photoluminescence quantum yield and stability achieved by encapsulating MAPbBr3 QDs in UIO-66 and their application in LEDs.

Lead halide perovskite quantum dots (QDs) have been extensively studied due to their excellent photoelectric performance. However, the stability of MAPbBr3 QDs is affected by inevitable factors such as light, heat, and moisture, which limits their practical applications. In this work, stable metal-organic framework UIO-66 was synthesized via a solvothermal method, and the composite MAPbBr3@UIO-66 was prepared through an in-situ growth method. Owing to the wide bandgap, small pore size, and regular geometric structure, UIO-66 can confine the size and uniformity of the perovskite QDs encapsulated within the framework, maximally preserving the luminescent properties of the perovskite QDs. Furthermore, UIO-66 isolates the perovskite QDs from contact with polar water molecules in the air, significantly enhancing the stability of the perovskite QDs. The synthesized composite material exhibits high stability and excellent optical performance, with a photoluminescence quantum yield (PLQY) of up to 78.9% in an air environment. After being stored under natural conditions for 35 days, it still retains 65% of its high luminescence intensity and fluorescence quantum efficiency. When packaged into green and white LEDs, the LEDs demonstrate high brightness and good monochromaticity, maintaining stable brightness even after 2.5 hours of continuous operation. These superior characteristics indicate that the composite material MAPbBr3@UIO-66 has great potential for application in LED technology.

On the influence of asphaltic molecules on the precipitation of acid-induced sludge: Molecular dynamics perspective

During the matrix acidizing treatment, asphaltic molecules precipitate solidly as a consequence of contact between acidic and oil phases at the oil–acid interface. Molecular dynamics simulation, a powerful tool, has not been utilized to investigate this phenomenon comprehensively. In the present study, this powerful technique was used to shed the light on the movement of polar molecules such as asphaltene and resin in the oil phase as well as hydronium ions in the aqueous acid phase toward the oil–acid interface during acid treatment. Additionally, the influence of significant variables such as crude oil type and asphaltene-to-resin ratio were studied. To achieve the aforementioned objectives, the oil and acidic phases were equilibrated separately under specific thermodynamic conditions and then the two phases were put into intimated contact. The precipitation of polar molecules during close contact of acid phase with paraffinic oil was opposite to aromatic oil for both high and low asphaltene-to-resin ratios. On the other hand, oil mixtures with equal number of asphaltene and resin molecules behaved differently. Our research indicates that the type of oil, either paraffinic or aromatic, has a significant effect on the formation of asphaltic sludge. Surprisingly, the influence of the asphaltene-to-resin ratio is so strong that it can offset the effect of the oil type. This is a result of the formation of micellar structures in the crude oil phase over a limited range of asphaltene-to-resin ratios. Additionally, more hydronium ions are attracted toward the interface in oil mixtures containing micelles.

Calculation of Some Low-Lying Electronic Excitations of Barium Monofluoride Using the Equation of Motion (EOM)-CC3 Method with an Effective Core Potential Approach.

Barium monofluoride (BaF) is a polar molecule of interest in measurements of the electron electric dipole moment. For this purpose, efforts are underway to investigate this molecule embedded within cryogenic matrices, e.g., in solid Ne. For a theoretical understanding of the electronic structure of such an embedded molecule, the need arises for efficient methods which are accurate but also able to handle a number of atoms which surround the molecule. The calculation for gas-phase BaF can be reduced to involve only outer electrons by representing the inner core of Ba with a pseudopotential, while carrying out a non-relativistic calculation with an appropriate basis set. Thus, the method is effectively at a scalar-relativistic level. In this work, we demonstrate to which extent this can be achieved using coupled-cluster methods to deal with electron correlation. As a test case, the SrF(X2Σ+→B2Σ+) transition is investigated, and excellent accuracy is obtained with the EOM-CC3 method. For the BaF(X2Σ+→A'2Δ, X2Σ+→A2Π, X2Σ+→B2Σ+) transitions, various coupled-cluster approaches are compared with very good agreement for EOM-CC3 with experimentally derived spectroscopic parameters, at the level of tens of cm-1. An exception is the excitation to the A'2Δ state, for which the energy is overestimated by 230cm-1. The poor convergence behavior for this particular state is demonstrated by providing results from calculations with basis sets of n = 3, 4, 5)-zeta quality. The calculated excitation energy for the B2Σ+ state agrees better with a deperturbation analysis than with the effective spectroscopic value, with a difference of 120cm-1.

Quantum sensing of ultralow temperature in biwire ultracold polar molecules

We present a systematic study of quantum sensing of ultralow temperature in biwire ultracold polar molecules of a quasi-one-dimensional (1D) trap by exploring the dynamics of two physically different qubit models. The two models consist of a trapped impurity atom that act as a temperature quantum sensor interacting with polar molecules reservoir, where dipole moments are aligned head-to-tail across the wires. Our model takes advantage of the adjustable interwire distance to accurately control the precision ultralow temperatures measurement. We show that the system undergoes a transition from Markovian to non-Markovian dynamics, which can be controlled by changing the interwire separation, the dipole-–dipole interaction (DDI), and the temperature. We characterize the thermometric performance using the quantum signal-to-noise ratio for both models and demonstrate that such a quantity exhibits a higher peak at ultralow temperature. We therefore emphasize that ultracold polar molecules are crucial for revolutionizing temperature sensing. Published by the American Physical Society 2024

Preparation and evaluation of a pyridine sulfonate betaine-based zwitterionic stationary phase for hydrophilic interaction chromatography

A zwitterionic stationary phase comprising pyridinium cations and sulfonate anions was successfully developed through thiol-ene click chemistry. Using seven polar small molecules as probes, the zwitterionic stationary phase showed high separation selectivity and excellent column efficiency (35,200–54,800 plates/m) compared with two commercial columns. The influence of water proportion, salt concentration, and pH in the mobile phase, and column temperature, on the retention of six polar compounds was examined. The retention mechanism was explored by three hydrophilic retention models, Tanaka test and linear solvation energy relationship analysis. For the analysis of sample dairy products (milk powder, milk, and yogurt), the stationary phase was operated in hydrophilic interaction chromatography mode without the addition of buffer salts, facilitating rapid and efficient detection and quantification of melamine. The LOD and LOQ are 0.04 mg⋅g−1 and 0.13 mg⋅g−1, respectively, and the recovery rate is 90.3 − 102.8 %. The zwitterionic stationary phase has the advantages of simple preparation, good method reproducibility, good selectivity and high precision.

Fabrication of ionic liquid-functionalized carbon dots as lubricant additive for friction and wear reduction

Herein, a long-chain ionic liquid with the catecholic group was successfully synthesized and then grafted to the carbon dots surface (CDs-ILs-Br) via the self-assembly capability of catecholic compound. The resulting CDs-ILs-Br exhibit excellent dispersion stability in PEG200, maintaining a uniform dispersion for over one month. With the addition of 3.0 wt% CDs-ILs-Br, the average COF of base oil decreased to 0.113, resulting in 60 % reduction in wear volume. Furthermore, the introduction of anti-wear agent BF4- further reduced average COF to 0.093. XPS and EDS analysis confirm complex tribochemical reactions between CDs-ILs-Br and the friction pair, and the grafting polar molecules of ILs on the carbon dots surface enhanced adhesion effect under high shear condition, forming a robust tribochemical protective film.

Polycyclic aromatic hydrocarbon derivatives onto polar microplastics of polyurethane: equilibrium, thermodynamics, and kinetics of monolayer-multilayer adsorption.

The study of the adsorption of polycyclic aromatic hydrocarbons on microplastics (MPs) has attracted much attention as to how microplastics can act as carriers of these pollutants. Polyurethane (PU) is one of the MPs found in aquatic environments, containing different functional groups it can interact with polar and nonpolar molecules. PAH derivatives (dPAHs) present different properties and thus can be adsorbed by different interactions; thus, this study investigated the adsorption of fluorene (FLN), dibenzothiophene (DBT), dibenzofuran (DBF), and carbazole (CBZ) onto PU MP. The Langmuir, Freundlich, and BET isotherm models were examined, and the BET model best fitted. The adsorption was a nonspontaneous process, exothermic for mono- and multilayer formation for FLN, DBT, and CBZ, and endothermic for DBF monolayer formation. The adsorption monolayer was formed by van der Waals forces, H─bonding, and π─π interactions, while the formation of the multilayer can be explained by π─π and hydrophobic interactions. The pseudo-second-order model proved to be more consistent for the adsorption of dPAHs. The adsorption in artificial seawater shows no significant differences for the monolayer but favored the adsorption multilayer due to the salting-out effect. Due to the existence of several adsorption mechanisms, PU MP interacts with dPAHs in greater quantities when compared to a MP with a simpler structure.

Two-axis twisting using Floquet-engineered XYZ spin models with polar molecules.

Polar molecules confined in an optical lattice are a versatile platform to explore spin-motion dynamics based on strong, long-range dipolar interactions1,2. The precise tunability3 of Ising and spin-exchange interactions with both microwave and d.c. electric fields makes the molecular system particularly suitable for engineering complex many-body dynamics4-6. Here we used Floquet engineering7 to realize new quantum many-body systems of polar molecules. Using a spin encoded in the two lowest rotational states of ultracold 40K87Rb molecules, we mutually validated XXZ spin models tuned by a Floquet microwave pulse sequence against those tuned by a d.c. electric field through observations of Ramsey contrast dynamics. This validation sets the stage for the realization of Hamiltonians inaccessible with static fields. In particular, we observed two-axis twisting8 mean-field dynamics, generated by a Floquet-engineered XYZ model using itinerant molecules in two-dimensional layers. In the future, Floquet-engineered Hamiltonians could generate entangled states for molecule-based precision measurement9 or could take advantage of the rich molecular structure for quantum simulation of multi-level systems10,11.

Rational Design of Fluorinated 2D Polymer Film Based on Donor-Accepter Architecture toward Multilevel Memory Device for Neuromorphic Computing.

Fluorine-containing 2D polymer (F-2DP) film is a desired system to regulate the charge transport in organic electronics but rather rarely reports due to the limited fluorine-containing building blocks and difficulties in synthesis. Herein, a novel polar molecule with antiparallel columnar stacking is synthesized and further embedded into an F-2DP system to control over the crystallinity of F-2DP film through self-complementary π-electronic forces. The donor-accepter-accepter'-donor' (D-A-A'-D') structure regulates the charge transportation efficiently, inducing multilevel memory behavior through stepwise charge capture and transfer processes. Thus, the device exhibits ternary memory behavior with low threshold voltage (Vth1 of 1.1V, Vth2 of 2.0V), clearly distinguishable resistance states (1:102:104) and ternary yield (83%). Furthermore, the stepwise formation of the charge complex endows the device with a wider range to regulate the conductive state, which allows its application in brain-inspired neuromorphic computing. Modified National Institute of Standards and Technology recognition can reach an accuracy of 86%, showing great potential in neuromorphic computing applications in the post-Moore era.

Surface Thermodynamic Properties of Styrene–Divinylbenzene Copolymer Modified by Supramolecular Structure of Melamine Using Inverse Gas Chromatography

The surface thermodynamic properties of polymers and copolymers modified by supramolecular structures are used in several industrial processes, such as selective adsorption, paints, coatings, colloids, and adhesion applications. Background: Inverse gas chromatography at infinite dilution was proved to be the best technique to determine the surface properties of solid surfaces by studying the adsorption of some model polar and non-polar organic molecules adsorbed on solid surfaces at different temperatures. Methods: The retention volume of adsorbed solvents is a valuable parameter that was used to obtain the London dispersive and polar free energies and the London dispersive surface energy of styrene–divinylbenzene copolymer modified by supramolecular structure of melamine using both the Hamieh thermal model and our new methodology consisting of the separation of the two polar molecules and the dispersive free energy of their interaction. This led to the determination of the polar acid and base surface energy, and the Lewis acid–base constants of the various solid materials. Results: Following our new methodology, all surface energetic properties of styrene–divinylbenzene copolymer modified by melamine at different percentages were determined as a function of temperature. Conclusions: It was observed that the styrene–divinylbenzene copolymer exhibited the highest London dispersive surface energy, which decreased when the melamine percentage increased. All materials presented higher Lewis basicity and this Lewis basicity increased with the percentage of melamine.

Power Dissipation of Uniaxial Anisotropic/Interacting Polar Molecules with Linear Reaction Dynamics in an Alternating Electric Field.

The influence of anisotropic potential energy and interaction between polar molecules on power absorption in chemical reactions with linear reaction dynamics in a weak alternating electric field is studied theoretically according to the reaction-diffusion equation. The expression for transient power loss is derived using two methods, electrodynamic method and equivalent circuit method, based on the electric energy conservation equation. Numerical calculations are carried out, and the results show that both the anisotropic potential energy and the interaction between polar molecules have a strong impact on energy dissipation and storage. For the anisotropic potential energy, when the applied dimensionless anisotropy is equal to 1, the power loss density increases about 32% at a low reaction rate and 27% at a high reaction rate compared to the case without anisotropic potential energy. When the dimensionless anisotropy is equal to -1, the power loss is suppressed and is reduced about 27% and 24% at low and high reaction rates, respectively. On the other hand, for the interaction between polar molecules, the power loss density decreases about 10% and 30% with low and high interaction potential energies, respectively. In addition, if the reaction rate is relatively high, the power loss will quickly decrease due to the end of the reaction process.

Small molecule π-π stacking promotes efficient photoelectrocatalytic splitting of aqueous hydrogen production from polyaniline.

The efficiency of photoelectrocatalysis is fundamentally dependent on the sufficient absorption of light and efficient utilisation of photogenerated carriers, but is largely limited by the reactivity from the inefficient charge transfer and surface sites of the catalyst. In this study, π-π stacking of polar small molecules on aromatic ring-rich polyaniline (PANI) was carried out to improve its photoelectrocatalytic splitting of water for hydrogen production. Detailed photoelectrochemical experiments and density-functional theory (DFT) calculations show that small molecules of p-aminobenzoic acid (PABA) and PANI have the best π-π stacking (compared to p-toluenesulfonic acid (PTA)), which promotes the separation of carriers on the PANI surface. In addition, the polar effect of the small molecules also improves the reactivity of the PANI surface and also reduces the potential barrier for H2 evolution. The current density of PANI-PABA reached -0.12 mA/cm2 (1.23 V vs. RHE) 2.53 times higher than that of pure PANI in linear voltammetric scanning tests under light. This strategy of introducing polar small molecules into organocatalysts via π-π stacking will provide new ideas for the preparation of efficient organic photoelectrocatalysis.

2D-3D cyclodextrin-modified montmorillonite assembly for efficient directional capture of amines

Shale gas exploitation produces a large amount of waste liquid, which cannot be fully recovered and discharged. Discharged wastewater contains several chemicals, including petroleum hydrocarbons, salts, and heavy metals. Amine compounds can absorb harmful gases but may lead to the presence of these compounds in wastewater. Some amine compounds may cause DNA mutations and health threats to humans and animals. Inspired by the assembly of artificial two-dimensional structures, this paper attempts to shape montmorillonite (MMT) with a natural layered structure. Specifically, a functional 2D/3D amine compound collector within the limitations of 2D MMT (Mt) was prepared by self-assembling cyclodextrin molecules. With the assembly of cyclodextrin (CD) molecules, the two-dimensional Mt. layer length increased from 12.14 to 19.11 Å. Adsorption experiments revealed that functional MMT powder (FMP) has good trapping ability for amines, that the adsorption of amine groups on FMP decreases with increasing temperature, and that it has greater potential to remove amine compounds with fewer carbon chains. Through molecular dynamics simulation, it was found that there was a molecular binding energy between FMP and branched polyethyleneimine (BPEI), indicating that FMP had a spontaneous adsorption effect on BPEI. Furthermore, their adsorption favored the Langmuir isotherm model and the pseudo-second-order kinetic model. This study also provides a new collector for the total organic carbon (TOC) advanced treatment system. Compared with that of ozone and UV treatment, the removal rate of FMP is 10 times higher than that of activated carbon and active resin, which can better remove polar molecules and is beneficial for gas field water recovery.