Glycol Research Articles

All-Layer Electrodeposition of a CdTe/Hg0.1Cd0.9Te/CdTe Photodetector for Short- and Mid-Wavelength Infrared Detection

CdS, CdTe, Hg0.1Cd0.9Te, CdTe, and Ag films were progressively electrodeposited on ITO-coated soda–lime glass to manufacture a short- and mid-wavelength infrared photodetector. A distinctive feature of the applied electrodeposition method is the use of a non-aqueous solution containing ethylene glycol (EG) as the electrolyte in a traditional three-electrode configuration for every film deposition. Using EG as a supplementary electrolyte and using the same deposition conditions with a potential below 0.75 V for all film coatings reduces their environmental incompatibility and offers a low-cost and low-energy route for fabricating the reported photodetector. The produced photodetector has a sensitivity of up to ≈957 nm with a detectivity (D*) of 2.86 × 1012 cm Hz1/2 W−1 and a dark current density (Jdark) of 10−6 mA cm−2. Furthermore, the manufactured photodiode exhibits self-powered performance because Voc and Jsc are self-generated, unlike previously reported photodiodes. The presented all-layer electrodeposition assembly approach can easily be adapted to fabricate sensing devices for different applications.

Normal-hexane treatment on PET-based waste fiber depolymerization process

Abstract The global increase in polyethylene terephthalate (PET)-based waste fiber poses a persistent environmental risk. While efforts have been made to repurpose waste fibers into bags, clothing, and building materials, the depolymerization process to extract pure raw materials for recycling remains underdeveloped. This study investigates the impact of normal hexane treatment on the purity of terephthalic acid (TPA) recovered from wastewater containing sodium terephthalate, ethylene glycol, and impurities generated during polyester fabric weight reduction or waste fiber recycling processes. Nuclear magnetic resonance analysis of the recovered TPA (rTPA) revealed a maximum purity of 99.81%, suggesting the effective removal of diverse contaminants such as adhesives and surfactants present in waste fibers through normal hexane and activated carbon treatments. This research contributes to the development of efficient and sustainable PET waste fiber recycling processes, highlighting the potential of normal hexane treatment in enhancing the purity of rTPA.

Micelles of poly[oligo(ethylene glycol) methacrylate] as delivery vehicles for zinc phthalocyanine photosensitizers

Drug-loaded polymeric micelles have proven to be highly effective carrier systems for the efficient delivery of hydrophobic photosensitizers (PSs) in photodynamic therapy (PDT). This study introduces the micellization potential of poly(oligoethylene glycol methyl ether methacrylate) (pOEGMA) as a novel approach, utilizing the hydrophobic methacrylate segments of pOEGMA to interact with highly hydrophobic zinc phthalocyanine (ZnPc), thereby forming a potential micellar drug carrier system. The ZnPc molecule was synthesized from phthalonitrile derivatives and its fluorescence, photodegradation, and singlet oxygen quantum yields were determined in various solvents. In solvents such as tetrahydrofuran, dimethyl sulfoxide, and N,N-dimethylformamide, the ZnPc compound exhibited the requisite photophysical and photochemical properties for PDT applications. The pOEGMA homopolymer was synthesized via reversible addition-fragmentation chain-transfer polymerization, while ZnPc-loaded pOEGMA micelles were prepared using the nanoprecipitation method. Characterization of the pOEGMA, ZnPc, and micelles was conducted using FTIR,1H-NMR, dynamic light scattering, matrix-assisted laser desorption/ionization time-of-flight mass spectrometries, gel permeation chromatography, and transmission electron microscopy. The critical micelle concentration was determined to be 0.027 mg ml-1using fluorescence spectrometry. The drug loading and encapsulation efficiencies of the ZnPc-loaded micelles were calculated to be 0.67% and 0.47%, respectively. Additionally, the release performance of ZnPc from pOEGMA micelles was monitored over a period of nearly 10 d, while the lyophilized micelles exhibited stability for 3 months. Lastly, the ZnPc-loaded micelles were more biocompatible than ZnPc on L929 cell line. The results suggest that the pOEGMA homopolymer possesses the capability to micellize through its methacrylate segments when interacting with highly hydrophobic molecules, presenting a promising avenue for enhancing the delivery efficiency of hydrophobic PSs in PDT. Moreover, it was also deciphered that obtained formulations were highly biocompatible according to cytotoxicity results and could be safely employed as drug delivery systems in further applications.

Effects of Dye Addition on the Rheological Properties of Aqueous Polymer Solutions.

In many commercial applications, polymer-dye interactions are frequently encountered from food to wastewater treatment, and while shear rheology has been well characterized, the extensional properties are not well known. The extensional viscosity ηE and relaxation time λE are the extensional rheological parameters that provide valuable insights into how aqueous polymers respond during deformation, and this study investigated the effect of dyes on the extensional rheology of three different aqueous polymer solutions (e.g., anionic, cationic, and neutral) paired with two different dye salts (e.g., anionic and cationic) using drop pinch-off experiments. We have found that the influence of dyes on the pinch-off dynamics is complex but generally leads to a decrease in, for example, the apparent extensional relaxation time. We have utilized the dripping-onto-substrate method to probe the uniaxial deformation of widely used polymers such as xanthan gum (XG), poly(diallyldimethylammonium chloride) (PDADMAC), and poly(ethylene oxide) (PEO) as the anionic, cationic, and neutral polymers, respectively, paired with either fluorescein (Fl) or methylene blue (MB) as the anionic and cationic dyes, respectively. Polymer-dye pairs with opposite charges (e.g., XG-MB and PDADMAC-Fl) displayed a pronounced decrease in pinch-off times, but even PEO, which is a neutral polymer, resulted in decreased pinch-off times, which was restored by the addition of NaCl. The pinch-off times for the Boger fluid (mixture of poly(ethylene glycol) and PEO), however, were surprisingly uninfluenced by dyes. These results showed that not only did the small addition of dyes strongly decrease the polymer relaxation times, but the relative importance of the dye salts on the polymer pinch-off dynamics was also different from that of pure salts such as NaCl.

Effect of particle size on SiO2 nanofluid viscosity determined by a two-step method

AbstractAccording to review of the literature, the influence of nanoparticle diameter with irregular shapes on viscosity requires further research since there is no relation between particle size and nanofluid stability. In this study, SiO2/EG–water-based nanofluid samples were prepared, and their viscosities were experimentally determined. SiO2 nanoparticles had sizes of 7, 15, and 40 nm, and the base fluid was a 50% ethylene glycol and 50% water mixture. Nanofluid samples were prepared using a two-step technique. Viscosity change was measured every 10 °C from 20 to 60 °C. The maximum viscosity values were observed for 7, 15, and 40 nm particles over an entire concentration range. Considering all measurements, the highest viscosity increase was 60.51% for 3% SiO2 (7 nm) at 60 °C, and the lowest viscosity change was 7.72% for 1% SiO2 (40 nm) at 40 °C. The most stable sample of the current study was 1% SiO2 (15 nm), and its Zeta potential was − 35.6 mV. Finally, a new empirical equation that included temperature, particle diameter, and concentration terms is suggested to predict dynamic viscosity, with R adj 2 = 0.98. It was also compared with previous correlations.

Design of Cyborg Proteins by Loop Region Replacement with Oligo(ethylene glycol): Exploring Suitable Mutations for Cyborg Protein Construction Using Machine Learning

Abstract We synthesized a “cyborg protein,” wherein a synthetic molecule partially substitutes the main peptide chain by linking two protein domains with a synthetic oligomer. Green fluorescent protein (GFP) served as the model for constructing the cyborg proteins. We prepared circularly permuted GFP (cpGFP) with new termini between β10 and β11, where the original N- and C-termini were linked by a cleavable peptide loop. The cyborg GFP was constructed from cpGFP by linking the β10 and β11 with oligo(ethylene glycol) using maleimide-cysteine couplings, followed by the enzymatic cleavage of the N- and C-termini linking loop by thrombin. With the help of machine learning, we were able to obtain the cpGFP mutants that significantly alter the fluorescence activity (53% increase) by thrombin treatment, which splits cpGFP into two fragments (fragmented-GFP), and by heat shock. When the cyborg GFP was constructed using this mutant, the fluorescence intensity increased by 13% after heat treatment, similar to cpGFP (33% increase), and the behavior was significantly different from that of the fragmented-GFP. This result suggests the possibility that the oligo(ethylene glycol) chain in the cyborg protein plays a similar role to the peptide in the main chain of the protein.

Unraveling the Impact of Oxygen Vacancy on Electrochemical Valorization of Polyester Over Spinel Oxides.

Electrochemical upcycling of end-of-life polyethylene terephthalate (PET) using renewable electricity offers a route to generate valuable chemicals while processing plastic wastes. However, it remains a huge challenge to design an electrocatalyst with reliable structure-property relationships for PET valorization. Herein, spinel Co3O4 with rich oxygen vacancies for improved activity toward formic acid (FA) production from PET hydrolysate is reported. Experimental investigations combined with theoretical calculations reveal that incorporation of VO into Co3O4 not only promotes the generation of reactive hydroxyl species (OH*) species at adjacent tetrahedral Co2+ (Co2+ Td), but also induces an electronic structure transition from octahedral Co3+ (Co3+ Oh) to octahedral Co2+ (Co2+ Oh), which typically functions as highly-active catalytic sites for ethylene glycol (EG) chemisorption. Moreover, the enlarged Co-O covalency induced by VO facilitates the electron transfer from EG* to OH* via Co2+ Oh-O-Co2+ Td interaction and the following C─C bond cleavage via direct oxidation with a glyoxal intermediate pathway. As a result, the VO-Co3O4 catalyst exhibits a high half-cell activity for EG oxidation, with a Faradaic efficiency (91%) and productivity (1.02mmol cm-2 h-1) of FA. Lastly, it is demonstrated that hundred gram-scale formate crystals can be produced from the real-world PET bottles via two-electrode electroreforming, with a yield of 82%.

Gold supported on Bi2MoO6 based on oxygen vacancy structure: Enhanced adsorption activation for efficient photocatalytic selective oxidation of benzyl alcohol

In this work, ethylene glycol was used as a mild reducing agent to prepare Bi2MoO6 support with oxygen vacancies. By introducing Au active species, an Au/BMO-Ov (Bi2MoO6 support with oxygen vacancies) photocatalyst was synthesized, which was co-modified with oxygen vacancies and Au NPs (nanoparticles), and significantly improved the capability of Bi2MoO6 for visible light-driven BA (benzyl alcohol) conversion. The 1wt% Au/BMO-Ov exhibited the highest conversion (98.8%) of BA and excellent selectivity (97.4%) of BAD (benzaldehyde) under visible light. Oxygen vacancies have an inhibitory effect on the recombination of photogenerated carriers. Au NPs acted as both photosensitizers (LSPR effect captures light and generates electrons and holes) and active species (used as Lewis acids). The results of photoelectrochemistry (PEC) tests confirmed that the synergistic interaction of Au and oxygen vacancies enhanced the photoactivity of bismuth molybdate. Meanwhile, density functional theory (DFT) calculations indicated that oxygen vacancies and Au synergistically reduced the bandgap energy of Bi2MoO6 and enhanced the adsorption of BA. Au served as the Lewis acid site for adsorption of BA, and improved the reactivity of light-driven BA conversion. The corresponding mechanism was proposed based on the experimental results and DFT calculations.

Rapid photo-crosslinking, highly conductive, and anti-freezing acrylamide-based hydrogels applied for ECG sensors

In recent years, ionic conductive hydrogels have attracted significant attention in the wearable sensors field due to their simplified preparation process, cost- effectiveness, and high conductivity. However, a large amount of water in traditional hydrogels inevitably condense into ice at low temperatures and make them lose various properties in their practical applications. Hence, this study proposes a method to rapidly synthesized a water/glycerol binary anti-freezing hydrogel only in 10s through photo-initiated free-radical polymerization. The introduction of LiCl into the crosslinked network composed of acrylamide (AAm) and poly (ethylene glycol) diacrylate (PEGDA) regulated the ionic conductivity of the hydrogel. The hydrogel exhibits a fracture strain of 1062.1%, a tensile strength of 31 kPa, and an adhesive strength of 6.49 kPa. The synergistic effects of glycerol and LiCl imparted excellent anti-freezing properties (−60 °C). The three-dimensional network structure of the hydrogel facilitates ion transport, exhibiting superior conductivity (30.25S/m), maintaining high conductivity capability of 1.46S/m even at a low temperature of −55 °C. Notably, the hydrogel demonstrates prolonged durability and stability in real-time human motion monitoring applications while concurrently exhibiting remarkable sensitivity as an ECG sensor. Hence, this as-prepared hydrogel can adapt to extreme environments and deliver comprehensive performance as an ECG sensor.

Effect of surfactant PEG on the property control of Bi2O3 and its photocatalytic activity

A detailed investigation into the effect of the poly(ethylene glycol) (PEG) addition mass on the bismuth (III) oxide (Bi2O3) photocatalyst is limited but necessary. Bismuth (III) oxide/PEG photocatalysts with different morphologies were prepared with different PEG mass via the solvothermal method and characterized for phase, morphology, optical absorption properties, elemental composition and specific surface area. The results indicated that all bismuth (III) oxide photocatalysts with different additions (Bi2O3/PEG-m x ) were pure β-bismuth (III) oxide phases, comprising larger platelike and smaller particle-like particles. Enhanced photocatalytic activity was attributed to increased larger specific surface area with PEG below 10 g. With 12 g of PEG, the formation of surface pores on plate-like bismuth (III) oxide impoved light penetration and utilization. Bi2O3/PEGm12 exhibited optimal photocatalytic activity, achieving over 90% bisphenol A(BPA) degradation after 180 min at 0.6 g·L−1 under visible light. Bismuth (III) oxide /PEG-ty prepared below 140°C showed poor activity, while above 160°C, high activity was observed. Bismuth (III) oxide/PEG effectively mineralize over 80% of bisphenol A into inorganic molecules and water under the co-oxidation of superoxide radicals (·O2 −) and holes (h+). This is the first detailed research on the regulation and modification of β-bismuth (III) oxide by PEG, which may provide new insights into the photocatalytic technology.

Kinetic and Thermodynamic Analysis of H2S Absorption by a Non-aqueous Absorbent of Monoethanolamine /Ethylene Glycol

Kinetic and Thermodynamic Analysis of H2S Absorption by a Non-aqueous Absorbent of Monoethanolamine /Ethylene Glycol

Tailor-made polymer tracers reveal the role of clay minerals on colloidal transport in carbonate media

HypothesisHost rock weathering and incipient pedogenesis result in the exposition of minerals, e.g., clay minerals in sedimentary limestones. Once exposed, these minerals provide the surfaces for fluid–solid interactions that control the fate of dissolved or suspended compounds such as organic matter and colloids. However, the functional and compositional diversity of organic matter and colloids limits the assessment of reactivity and availability of clay mineral interfaces. Such assessment demands a mobile compound with strong affinity to clay surfaces that is alien to the subsurface. ExperimentWe approached this challenge by using poly(ethylene glycol) (PEG) as interfacial tracer in limestone weathering experiments. FindingsPEG adsorption and transport was dependent on the availability of clay mineral surfaces and carbonate dissolution dynamics. In addition, PEG adsorption featured adsorption–desorption hysteresis which retained PEG mass on clay mineral surfaces. This resulted in different PEG transport for experiments conducted consecutively in the same porous medium. As such, PEG transport was reconstructed with a continuum-scale model parametrized by a Langmuir-type isotherm including hysteresis. Thus, we quantified the influence of exposed clay mineral surfaces on the transport of organic colloids in carbonate media. This renders PEG a suitable model colloid tracer for the assessment of clay surface exposition in porous media.

Green Fabrication Methods and Performance Evaluation of Eco-Friendly Membranes for Enhanced Oil-Water Separation

A significant step toward sustainability in membrane technology has been made with the substitution of eco-friendly alternatives for conventional membrane fabrication techniques. A green fabrication process, which is derived from renewable and biodegradable materials, offers a promising solution to environmental concerns associated with conventional membrane fabrication. Additionally, by utilizing eco-friendly materials, the toxicity footprint of membrane fabrication techniques can be reduced considerably. This study aims to transform the non-solvent induced phase separation (NIPS) method into a green process, by utilizing a biodegradable polymeric base (polylactic acid; PLA), a green solvent (dimethyl sulfoxide; DMSO), and a green additive (deep eutectic solvents; DES). The membranes were thoroughly characterized to understand their structural transformations, and their performance was evaluated. Filtration experiments demonstrated a notable increase in the water flux using 20wt% PLA polymer, DMSO as a solvent, and 1wt% choline chloride: ethylene glycol (ChCl:EG) (1:2) as an additive. This resulted in a flux of 1138L/m2.h, a notable increase compared to 554L/m2.h achieved with 20wt% PLA using a conventional solvent (PLA-C). This increase in flux was also complemented by an increase in the membrane's oil rejection efficiency, (oil rejection of 96% for the modified membrane), as well as enhanced anti-fouling properties (maintained in interval flux recovery ratio; FRR of 80%). The findings suggest that creating environmentally friendly membranes through a sustainable process has the potential to improve both ecological impact and performance, hence progressing environmentally conscious industrial practices.

Sustainable catalytic pathways for biofuel precursors: quantitative conversion of glucose to gluconic acid using Pt-Zn biochar catalyst

Achieving quantitative conversion of biomass-derived feedstocks under ambient environmental conditions (20°C, atmospheric air, 0.1 MPa) is a critical milestone for sustainability in chemical processes. Herein, the quantitative conversion of glucose to gluconic acid was accomplished under ambient environmental conditions without any additives using a Pt-Zn intermetallic nanoparticle-supported biochar catalyst prepared from raw rice straw (Pt-Zn/strawC) via a straightforward one-pot solvothermal reaction with ethylene glycol solvent. Spectroscopic analyses verified the formation of the Pt-Zn intermetallic alloy and confirmed strong electronic metal-support interactions. The Pt-Zn/strawC catalyst (Pt:Zn molar ratio of 1:6) was highly selective for the conversion of glucose to gluconic acid, whereas yields as high as 99.9% (98.9% gluconic acid, 1.0% glucaric acid) were reached at 20 oC under base-free and additive-free conditions. Isotope measurements and density functional theory revealed synergistic interactions in the Pt-Zn alloy, wherein the alloy tended to absorb glucose and active O2 into superoxide radical (O2·). This work demonstrates a chemocatalytic method that is practical for environmental conditions and provides a new avenue for sustainable conversion of lignocellulosic biomass to chemical products.

Incorporation of myrtle essential oil into hydrolyzed ethyl cellulose films for enhanced antimicrobial packaging applications

This research delved into examining the impact of hydrolysis and incorporation of Myrtle essential oil (MEO) on the film-forming and antimicrobial characteristics of ethyl cellulose polymer (EC). Three plasticizers (glycerol, mono ethylene glycol, and oleic acid) were evaluated for film-forming ability. The composite biofilms' structure was assessed through SEM, XRD, FT-IR, and DSC. Eventually, the combination of hydrolyzed EC with oleic acid yielded a flexible film with optimal thickness. Utilizing GC-MS analysis, α-pinene was identified as the predominant compound within MEO, conferring both antioxidant and antibacterial attributes. FTIR spectroscopy confirmed MEO's participation in the film-forming matrix through hydrogen bonding. By incorporating the MEO into the matrix, the WVP decreased significantly to 6.15*10-12 gmm/hmm2Pa considering that the hydrophobic feature of MEO can block the diffusion of water and decrease the WVP. The melting point and enthalpy of the polymer matrix containing MEO decreased that could be attributable to the EOs plasticizing impact, which increases the polymer chain mobility, and thereby hinders the strong interactions between polymer molecules. From the morphological finding, even at higher concentrations, MEO did not form agglomerations in the film matrix, highlighting its excellent compatibility with the microstructure of the resulting films. The film containing MEO showed the acceptable antioxidant activity. Furthermore, films containing MEO substantially decreased S. aureus biofilm development at 24 and 48 hours, compared to P. aeruginosa and E. coli. These findings suggest potential applications of the developed film in packaging and preservation.

Comparative studies on pinhole free CBD-CdZnS thin films on ITO and FTO substrate

The development of CdZnS thin films using the chemical bath deposition process in nonaqueous media is a technological challenge. In this work, 75 millilitres of ethylene glycol and ethanol (1:2 ratios) were used to develop a CdZnS thin film on ITO and FTO glass substrates using cadmium acetate, zinc sulphate, and thiourea. The ideal bath temperature was kept at 1300C and the anneal temperature of the film that had been deposited in the air was maintained at 3500C. The films have been examined using FTIR, WCA, FESEM, and XRD. XRD studies reveal that CdZnS films have a hexagonal crystal structure with a preference for orientation (002) during the deposition and annealing processes and the assessment of the various attributes have been done, such as dislocation density, micro strain, and grain size. FESEM study indicates that as deposited film on ITO glass have smooth surface and grains appear in the form of small needle shape of equal sizes where as FTO substrate reveals the grains of equal size throughout the entire surface in cluster form. It is also confirmed that both the CdZnS films formed on ITO and FTO substrates have hydrophilic quality. The presence of chemical bonds and functional groups was confirmed by FTIR analysis.

P19-49 In vitro and PBTK models to assess the hepatic and extra-hepatic metabolism of propylene glycol ethers in the context of CNS toxicity

P19-49 In vitro and PBTK models to assess the hepatic and extra-hepatic metabolism of propylene glycol ethers in the context of CNS toxicity

Simultaneous therapeutic and diagnostic applications of magnetic PLGA nanoparticles loaded with doxorubicin in rabbit.

In this study, DOX (Doxorubicin) and Fe3O4 magnetic nanocrystals (SPIONs (Superparamagnetic iron oxide nanocrystals)) were encapsulated in the PLGA-PEG: poly(lactide-co-glycolide)-b-poly(ethylene glycol) nanoparticles for theranostic purposes. The final prepared formulation which is called NPs (Nanoparticles) exhibited a particle size with a mean diameter of ~ 209nm and a sufficient saturation magnetization value of 1.65 emu/g. The NPs showed faster DOX release at pH 5.5 compared to pH 7.4. Also, the cytotoxicity effect of NPs increased compared to Free-DOX alone in C6 glioma cancer cells. For in vivo investigations, the 2.2 Kg rabbits were injected with NPs formulations via a central articular anterior vein in their ears. Furthermore, the images of rabbit organs were depicted via MR (Magnetic resonance) and fluorescent imaging techniques. A negative contrast (dark signal) was observed in T2 (Relaxation Time) weighted MR images of IV (Intravenously)-injected rabbits with NPs compared to the control ones. The organ's florescent images of NPs-injected rabbits showed a high density of red color related to the accumulation of DOX in liver and kidney organs. These data showed that the NPs have no cytotoxicity effect on the heart. Also, the results of histopathological tests of different organs showed that the groups receiving NPs and Free-DOX were almost similar and no significant difference was seen, except for the cardiac tissue in which the pathological effects of NPs were significantly less than the Free-DOX. Additionally, pharmacokinetic studies were also conducted at the sera and whole bloods of IV-injected rabbits with NPs and Free-DOX. The pharmacokinetic parameters showed that NPs could enhance the DOX retention in the serum compared to the Free-DOX. Altogether, we aimed to produce a powerful delivery nanosystem for its potential in dual therapeutic and diagnostic applications which are called theranostic agents.

The Application of Green Solvents in the Synthesis of S-Heterocyclic Compounds—A Review

Cyclic organic compounds containing sulfur atoms constitute a large group, and they play an important role in the chemistry of heterocyclic compounds. They are valuable intermediates for the synthesis of other compounds or biologically active compounds themselves. The synthesis of heterocyclic compounds poses a major challenge for organic chemists, especially in the context of applying the principles of “green chemistry”. This work is a review of the methods of synthesis of various S-heterocyclic compounds using green solvents such as water, ionic liquids, deep eutectic solvents, glycerol, ethylene glycol, polyethylene glycol, and sabinene. The syntheses of five-, six-, and seven-membered heterocyclic compounds containing a sulfur atom or atoms, as well as those with other heteroatoms and fused-ring systems, are described. It is shown that using green solvents determines the attractiveness of conditions for many reactions; for others, such use constitutes a real compromise between efficiency and mild reaction conditions.

Immobilization of Lipase from Thermomyces Lanuginosus and Its Glycerolysis Ability in Diacylglycerol Preparation

In the glycerolysis process for diacylglycerol (DAG) preparation, free lipases suffer from poor stability and the inability to be reused. To address this, a cost-effective immobilized lipase preparation was developed by cross-linking macroporous resin with poly (ethylene glycol) diglycidyl ether (PEGDGE) followed by lipase adsorption. The selected immobilization conditions were identified as pH 7.0, 35 °C, cross-linking agent concentration 2.0%, cross-linking time 4 h, lipase amount 5 mg/g of support, and adsorption time 4 h. Enzymatic properties of the immobilized lipase were analyzed, revealing enhanced pH stability, thermal stability, storage stability, and operational stability post-immobilization. The conditions for immobilized enzyme-catalyzed glycerolysis to produce DAG were selected, demonstrating the broad applicability of the immobilized lipase. The immobilized lipase catalyzed glycerolysis reactions using various oils as substrates, with DAG content in the products ranging between 35 and 45%, demonstrating broad applicability. Additionally, the changes during the repeated use of the immobilized lipase were characterized, showing that mechanical damage, lipase leakage, and alterations in the secondary structure of the lipase protein contributed to the decline in catalytic activity over time. These findings provide valuable insights for the industrial application of lipase.