Adipic Acid Research Articles

Preparation and properties of ambient self-crosslinking acrylic emulsion

Abstract With styrene (St), butyl acrylate (BA), and methyl methacrylate (MMA) as monomers, a core-shell structure was utilized to synthesize a polymerization emulsion. Then, self-crosslinked polyacrylic acid emulsions with different crosslinking degrees were synthesized by changing the amount of DAAM using deception acrylamide (DAAM) and adipic acid dihydrazide (ADH) as functional monomers. The basic performance tests demonstrated that the inclusion of DAAM resulted in an increase in the emulsion’s stability and film’s solvent resistance; The DSC test demonstrated that boosting the crosslinking degree was advantageous in improving the T g of the film; according to FT-IR and microscopic tests, the crosslinking reaction took place in the system. The self-crosslinking acrylic emulsion of this system has a certain application prospect as a binder.

Effect of laser irradiation on the growth of Adipic acid single crystal for NLO applications

Effect of laser irradiation on the growth of Adipic acid single crystal for NLO applications

Degradation of polylactic acid/polybutylene adipate-co-terephthalate blend by Papiliotrema laurentii S2P4P isolated from agricultural soils

Polylactic acid/polybutylene adipate-co-terephthalate blend (PLA/PBAT) has been widely used due to their good biodegradation. Recently, the biodegradation of PLA and PBAT has received increasing attention. However, PLA/PBAT blend-degrading strains have been rarely reported in comparison to that for pure PLA and PBAT. A fungus strain, Papiliotrema laurentii S2P4P, was isolated from agricultural soils and identified. S2P4P can efficiently degrade commercial PLA/PBAT films at 30°C in mineral salt medium (MSM) and obtained about 14% of weight loss within 30 days of incubation. Additionally, rough and uneven surface of PLA/PBAT film with cracks and creases, increased hydrophilicity, changes in mechanical property, and decreased intensity of C=O and C-O bonds were observed after S2P4P treatments. The strain secreted esterase to catalyze the degradation of the ester bonds in PLA/PBAT blend, resulting in the production of degradation products such as butanediol, adipic acid, lactic acid and terephthalic acid as well as their oligomers. Furthermore, as carbon and energy sources, the degradation products could participate in the metabolism of S2P4P and then accelerate degradation of PLA/PBAT blend. The advantages of P. laurentii S2P4P in simultaneous degradation of PLA and PBAT indicated that the strain has potential value for the bioremediation of PLA/PBAT blend in the actual environment.

Sustainable Adipic Acid Production via Paired Electrolysis of Lignin-Derived Phenolic Compounds with Water as Hydrogen and Oxygen Sources.

Adipic acid (AA) is an important feedstock for nylon polymers and is industrially produced from fossil-derived aromatics via thermocatalysis. However, this process consumes explosive H2 and corrosive HNO3 as reductants and oxidants, respectively. Here, we report the direct synthesis of AA from lignin-derived phenolic compounds via paired electrolysis using bimetallic cooperative catalysts. At the cathode, phenol is hydrogenated on PtAu catalysts to form ketone-alcohol (KA) oil with 92% yield and 43% Faradaic efficiency (FE). At the anode, KA is electrooxidized into AA on CuCo2O4 catalysts, achieving a maximum of 85% yield and 84% FE. Experimental and theoretical studies reveal that the excellent catalytic activity can be ascribed to the enhanced absorption and activation capability of reactants on the bimetallic cooperative catalysts. A two-electrode flow electrolyzer for AA synthesis realizes a stable electrolysis at 2.5 A for over 200 h as well as 38.5% yield and 70.2% selectivity. This study offers a green and sustainable route for AA synthesis from lignin via paired electrolysis.

Sonication-Induced Boladipeptide-Based Metallogel as an Efficient Electrocatalyst for the Oxygen Evolution Reaction.

Bioinspired, self-assembled hybrid materials show great potential in the field of energy conversion. Here, we have prepared a sonication-induced boladipeptide (HO-YF-AA-FY-OH (PBFY); AA = Adipic acid, F = l-phenylalanine, and Y = l-tyrosine) and an anchored, self-assembled nickel-based coordinated polymeric nanohybrid hydrogel (Ni-PBFY). The morphological studies of hydrogels PBFY and Ni-PBFY exhibit nanofibrillar network structures. XPS analysis has been used to study the self-assembled coordinated polymeric hydrogel Ni-PBFY-3, with the aim of identifying its chemical makeup and electronic state. XANES and EXAFS analyses have been used to examine the local electronic structure and coordination environment of Ni-PBFY-3. The xerogel of Ni-PBFY was used to fabricate the electrodes and is utilized in the OER (oxygen evolution reaction). The native hydrogel (PBFY) contains a gelator boladipeptide of 15.33 mg (20 mmol L-1) in a final volume of 1 mL. The metallo-hydrogel (Ni-PBFY-3) is prepared by combining 15.33 mg (20 mmol L-1) of boladipeptide (PBFY) with 3 mg (13 mmol L-1) of NiCl2·6H2O metal in a final volume of 1 mL. It displays an ultralow Tafel slope of 74 mV dec-1 and a lower overpotential of 164 mV at a 10 mA cm-2 current density in a 1 M KOH electrolyte, compared to other electrocatalysts under the same experimental conditions. Furthermore, the Ni-PBFY-3 electrocatalyst has been witnessed to be highly stable during 100 h of chronopotentiometry performance. To explore the OER mechanism in an alkaline medium, a theoretical calculation was carried out by employing the first-principles-based density functional theory (DFT) method. The computed results obtained by the DFT method further confirm that the Ni-PBFY-3 electrocatalyst has a high intrinsic activity toward the OER, and the value of overpotential obtained from the present experiment agrees well with the computed value of the overpotential. The biomolecule-assisted electrocatalytic results provide a new approach for designing efficient electrocatalysts, which could have significant implications in the field of green energy conversion.

Anthropogenic organic matter influence on epicuticular Tillandsia stricta Sol. ex Sims and Tillandsia usneoides (L.) L. (Bromeliaceae) wax leaf from Rio de Janeiro sandbank

Epicuticular wax from the leaves of Tillandsia stricta Sol. Sims and Tillandsia usneoides (L.) from Grumari, Marica and Jurubatiba, Rio de Janeiro sandbanks was extracted into chloroform and n-hexane for analyses. The extracts were subjected to gas chromatography (GC-FID) and gas chromatography coupled with mass spectrometry (GC-MS) analyses. In the investigated species, the major n-alkane was found to be C-27. This study has shown that the relation of n-alkanes and fatty acids is a function of the species and the triterpenoids were only observed in the wax of T. usneoides. Phthalates: di-n-octyl phthalate (DNOP), di isobutyl phthalate (DIBP); Di (2-ethylhexyl) phthalate (DEHP), benzoic acid, adipic acid derivatives were also detected beyond of DDT in T. stricta from the Conservation Unit of Jurubatiba. The exposure of T. usneoides to vehicular emission resulted in the reversal of the relationship fatty acid: n-alkanes and the triterpenoids suppression. These results reflect the importance of plants in monitoring environmental purposes and their potential for DDT and phthalates indicator.

Quality by design approach for fabrication of extended-release buccal films for xerostomia employing hot-melt extrusion technology

The study endeavors the fabrication of extended-release adipic acid (APA) buccal films employing a quality by design (QbD) approach. The films intended for the treatment of xerostomia were developed utilizing hot-melt extrusion technology. The patient-centered quality target product profile was created, and the critical quality attributes were identified accordingly. Three early-stage formulation development trials, complemented by risk assessment aligned the formulation and process parameters with the product quality standards. Employing a D-optimal mixture design, the formulations were systematically optimized by evaluating three formulation variables: amount of the release-controlling polymer Eudragit® (E RSPO), bioadhesive agent Carbopol® (CBP 971P), and pore forming agent polyethylene glycol (PEG 1500) as independent variables, and % APA release in 1, 4 and 8 h as responses. Using design of experiment software (Design-Expert®), a total of 16 experimental runs were computed and extruded using a Thermofisher ScientificTM twin screw extruder. All films exhibited acceptable content uniformity and extended-release profiles with the potential for releasing APA for at least 8 h. Films containing 30% E RSPO, 10% CBP 971P, and 20% PEG 1500 released 88.6% APA in 8 h. Increasing the CBP concentration enhanced adhesiveness and swelling capacities while decreasing E RSPO concentration yielded films with higher mechanical strength. The release kinetics fitted well into Higuchi and Krosmeyer-Peppas models indicating a Fickian diffusion release mechanism.

Effect of Intensification of the Tricarboxylic Acid Cycle on Biosynthesis of Adipic Acid Through the Inverted Fatty Acid β-Oxidation by Escherichia coli Strains

Effect of Intensification of the Tricarboxylic Acid Cycle on Biosynthesis of Adipic Acid Through the Inverted Fatty Acid β-Oxidation by Escherichia coli Strains

Computation-guided transcription factor biosensor specificity engineering for adipic acid detection

Transcription factor (TF)-based biosensors that connect small-molecule sensing with readouts such as fluorescence have proven to be useful synthetic biology tools for applications in biotechnology. However, the development of specific TF-based biosensors is hindered by the limited repertoire of TFs specific for molecules of interest since current construction methods rely on a limited set of characterized TFs. In this study, we present an approach for engineering the specificity of TFs through a computation-based workflow using molecular docking that enables targeted alteration of TF ligand specificity. Using this method, we engineer the LysR family BenM TF to alter its specificity from its cognate ligand cis,cis-muconic acid to adipic acid through a single amino acid substitution identified by our computational workflow. When implemented in a cell-free system, the engineered biosensor shows higher ligand sensitivity, expanding the potential applications of this circuit. We further investigate ligand binding through molecular dynamics to analyze the substitution, elucidating the impact of modulating a single amino acid position on the mechanism of BenM ligand binding. This study represents the first application of biomolecular modeling methods for altering BenM specificity and for gaining insights into how mutations influence the structural dynamics of BenM. Such methods can potentially be applied to other TFs to alter specificity and analyze the dynamics responsible for these changes, highlighting the applicability of computational tools for informing experiments. In addition, our developed adipic acid biosensor can be applied for the identification and engineering of enzymes to produce adipic acid.

Effect of Dicarboxylic Acid Chain Length on the Tribological Properties of Aqueous Polyether Esters

ABSTRACTThis article presents the preparation of environmentally friendly water‐soluble lubricant additives. Adipic acid (AA), sebacic acid (SA) and dodecanedioic acid (DA) were individually subjected to esterification reactions with polyethylene glycol 1500 (PEG1500) to prepare a class of water‐soluble polyether esters (AAPEE1500, SAPEE1500 and DAPEE1500) (referred to as XAPEE1500s) that exhibit excellent water solubility and do not contain environmentally harmful elements. First, the molecular structure characterisation and functional group analysis of these additives will be conducted using an infrared spectrometer and a nuclear magnetic resonance spectrometer. Subsequently, the frictional properties of the additives in the base liquid (deionised water) will be investigated using an SRV‐V tribometer, Falex pin‐on‐disc tribometer and screw torque tester. The surface morphology of wear scars will be characterised and analysed using scanning electron microscopy (SEM) and a non‐contact 3D profilometer. Finally, the lubrication mechanism of the DAPEE1500 additive will be analysed using X‐ray photoelectron spectroscopy (XPS). The results indicate that the optimal lubrication performance is achieved when the added mass fraction of DAPEE1500 is at 3%. Compared with 0.5 wt% DAPEE1500, the average friction coefficient of 3 wt% DAPEE1500 decreased from 0.285 to 0.122, and the wear volume decreased from 25.52 × 10−5 μm3 to 10.96 × 10−5 μm3. The lubrication mechanism of polyether ester is the result of the combined action of its polar ester functional groups and long carboxylic acid chains in the structure. These polar functional groups can form a relatively firm adsorption film on the friction surface, while the long carboxylic acid chains act as a brush‐like isolating layer, thus demonstrating superior anti‐wear and anti‐friction performance.

Control of Microcystis aeruginosa by Daphnia: Experimental evidence and identification of involved infochemicals.

Infochemicals refer to chemicals responsible for information exchange between organisms. We evaluated the effects of Daphnia magna and Daphnia galeata infochemicals on Microcystis aeruginosa for 15d. The Daphnia infochemicals were obtained from spent medium after culturing Daphnia in Elendt M4 medium for 48 h. Both Daphnia infochemicals significantly increased (p < 0.05) the intracellular reactive oxygen species level and microcystin-LR concentration in M. aeruginosa. This cellular effect increased colony formation of M. aeruginosa, thereby inhibiting the growth of M. aeruginosa. D. galeata infochemicals provoked significantly greater (p < 0.05) adverse effects on M. aeruginosa than those of D. magna infochemicals, which were further exaggerated by pre-exposure of Daphnia to M. aeruginosa. This result seems to be related to the different compositions and concentrations of Daphnia infochemicals. Several Daphnia infochemicals, such as methyl ferulate, cyclohexanone, 3, 5-dimethyl, hexanedioic acid, and bis(2-ethylhexyl) ester, showed a high correlation with M. aeruginosa cell concentration (|r | >0.6), suggesting that they may play a key role in controlling harmful cyanobacteria. Additionally, pre-exposure of D. magna and D. galeata to M. aeruginosa produced oleic acid, methyl ester, and n-hexadecanoic acid, with a highly correlation with M. aeruginosa cell concentration (|r | >0.6). p-tolyl acetate and linoleic acid were detected only in the pre-exposed D. galeata infochemicals. These findings suggest that some of Daphnia infochemicals identified in this study can be a promising tool to control M. aeruginosa growth. However, further studies are required to verify the specific actions of these infochemicals against cyanobacteria.

Analytical strategy to assess the microbial degradation of poly(butylene-adipate-co-terephthalate)/poly(lactic acid) films

Plastic is widely used in agricultural applications, but its waste has an adverse environmental impact and a long-term detrimental effect. The development of biodegradable plastics for agricultural use is increasing to mitigate plastic waste. The most commonly used biodegradable plastic is poly(butylene adipate co-terephthalate)/poly(lactic acid) (PBAT/PLA) polymer.In this study, an analytical procedure based on dispersive liquid-liquid microextraction (DLLME) followed by gas chromatography-mass spectrometry (GC-MS) in combination with chemometrics has been optimized to assess the degradation level of PBAT/PLA films by monitoring their characteristic degradation products. Carboxylic acids (benzoic, phthalic, adipic, heptanoic, and octadecanoic acids) and 1,4-butanediol have been found to be potential markers of PBAT/PLA degradation.The DLLME-GC-MS analytical approach has been applied for the first time to assess the degradation efficiency of several microorganisms used as degradation accelerators of PBAT/PLA based on the assigned potential markers. This analytical strategy has shown higher sensitivity and precision than standard techniques, such as elemental analysis, allowing us to detect low degradation levels.

Ultrafiltration membrane based on chitosan/adipic acid: Synthesis, characterization and performance on separation of methylene blue and reactive yellow-145 from aqueous phase

Here, we report for the first time using of the nontoxic chitosan/adipic acid cross-linked membrane CS/AA in the separation of methylene blue and reactive yellow-145 from aqueous phase. The reason we chose adipic acid as a cross-linking agent is because it gives the cross-linked membrane moderate flexibility due to the presence of four methylene groups in its structure. The structure of the cross-linked membrane CS/AA and their properties were confirmed through, FTIR, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), atomic force microscopy (AFM), and BET analysis. The thermal properties of membrane indicated an improvement in its flexibility and hydrophobicity, but this improvement was accompanied by a decrease in its thermal stability. pHpzc value and porosity of the CS/AA were 7.88, and 73.95 % respectively. The average pore radius distribution ranged from 2 to 27 nm. The prepared cross-linked membrane provides spontaneous and continuous purification of water with a high efficiency. This is due to the membrane CS/AA ability to separate methylene blue and reactive yellow-145 from the aqueous phase almost completely. The results revealed that the removal efficiency and permeation flux for MB were 100 % and 1 L/m2.h respectively at initial dye concentration of (4,8) mg/L, at 1 bar, and the removal efficiency and permeation flux for RY-145 were (94,96) % and (1.06, 2.09) L/m2.h respectively at 100 mg/L and at (1,1.5) bar. Such cross-linked nanopore polymer membranes provide a new approach for emerging novel purification systems, principally in the field of environmental field.

Polybutylene adipate terephthalate (PBAT) composites for thermally conductive, fire retardant, high dielectric applications using BaTiO3 and MWCNTs as fillers

This study provides a comprehensive investigation of the fabrication of novel composite materials by blending polybutylene adipate terephthalate (PBAT) with barium titanate (BaTiO3) and multiwalled carbon nanotube (MWCNT) fillers. Prior to fabricating the composites, the filler surface treatments were tailored to enhance their compatibility with the PBAT matrix. Adipic acid (AA), a monomer for PBAT, was employed on the surface of the BaTiO3 particles, while butanediol (BD) also a monomer of PBAT was used to modify the surface of the MWCNTs to ensure effective interaction with the PBAT chains during the composite fabrication process. The composite samples were produced by melt-blending at 140 °C, followed by injection molding at the same operating temperature for subsequent analysis. The results revealed remarkable improvements in the dielectric constant, thermal conductivity, fire retardancy, and tensile strength of the 40 wt% BaTiO3 and MWCNT-PBAT blends compared to pure PBAT. The incorporation of BaTiO3 additionally contributed to enhanced fire retardancy, mechanical properties, and dielectric properties, making the composite material more resistant to ignition and flame spread, thus rendering it suitable for applications requiring elevated fire safety. In addition, the inclusion of MWCNT improved thermal conductivity, enabling promising and efficient heat dissipation in various applications.

Roseateles agri sp. nov., a New Species Isolated from Fresh Soil in Uiwang, South Korea

Two isolates of Roseateles were discovered in soil samples collected from Uiwang-si, Gyeonggi-do, Republic of Korea. These isolates exhibited rod-shaped morphology and were facultatively anaerobic, non-motile, and tested positive for oxidase and catalase. Designated as strains R3-3T and R3-11, their growth was hindered by NaCl concentrations exceeding 0.5%, while their optimal growth conditions were observed at temperatures ranging from 25 °C to 30 °C and pH levels between 7.0 and 9.0. Both strains exhibited positive results for the hydrolysis of Tween 80 and DNA, but tested negative for starch, casein, chitin, and gelatin hydrolysis. Additionally, they assimilated L-Arabinose, D-mannitol, and D-Maltose, while exhibiting negative results for the fermentation of D-glucose, esculin ferric citrate, D-mannose, N-acetyl-glucosamine, potassium gluconate, capric acid, adipic acid, trisodium citrate, and phenylacetic acid. The DNA G+C content of strain R3-3T was measured at 67.5 mol%. Comparative analysis revealed that the average nucleotide identity (ANI) values between R3-3T and the Roseateles type strains ranged from 75.14% to 78.30% while the digital DNA-DNA hybridization (dDDH) values ranged from 20.70% to 22.70%. Consequently, based on comprehensive genomic, chemotaxonomic, phenotypic, and phylogenomic evaluations, the isolated strains have been designated as a new species within the genus Roseateles, named Roseateles agri sp. nov. (with type strain R3-3T = KACC 23678T = NBRC 116681T).

Synthesis of Cycloaliphatic Polyamides via Palladium-Catalyzed Hydroaminocarbonylative Polymerization.

Polyamides represent one class of materials that is important in modern society. Because of the numerous potential applications of polyamides in various fields, there is a high demand for new polyamide structures, which necessitates the development of new polymerization methods. Herein, we report a novel and efficient palladium-catalyzed hydroaminocarbonylative polymerization of dienes and diamines for the synthesis of cycloaliphatic polyamides. The method employs readily available starting materials, proceeds in an atom-economic manner, and creates a series of new functional polyamides in high yields and high molecular weights. In contrast with the traditional polyamides based on adipic acid, the cycloaliphatic polyamides have superior thermal resistance, higher glass-transition temperature, and better solubility in common organic solvents, thus probably featuring the merits of high-performance and good processability.

PSII-13 Effects of benzoic acid, bromelain, adipic acid, and humic substance supplementation on nitrogen balance, urine pH, slurry pH, and manure odorous compounds in pigs

Abstract The objective of the present study was to evaluate the effects of benzoic acid, bromelain, adipic acid, and humic substance supplementation on nitrogen balance, urinary pH, slurry pH, and manure odorous compounds in pigs. Fifteen barrows with an initial body weight of 37.9 kg (standard deviation = 4.1) were individually housed in metabolism crates. The animals were allocated to a triplicated 5 × 2 incomplete Latin square design with 15 animals, 5 experimental diets, and 2 periods. The basal diet mainly consisted of corn, soybean meal, and rapeseed meal. Four experimental diets were prepared by supplementing each additive at a concentration of 10 g/kg at the expense of corn starch to the basal diet. Each period consisted of a 4-d adaptation period and a 24-h collection period for slurry, followed by a 4-d collection period for feces and urine. On d 5, feces and urine were collected for 24 h, and the feces and urine were mixed in a ratio of fecal weight to urine weight at the end of the collection to obtain slurry samples. The fecal nitrogen (N) output was greatest (P &amp;lt; 0.05) in pigs fed the diet supplemented with humic substances. The apparent total tract digestibility of N in pigs fed the humic substance diet was less (P &amp;lt; 0.05) than other groups. The urinary pH in pigs fed the adipic acid diet was less (P &amp;lt; 0.05) than that in other groups except the benzoic acid group. The slurry pH tended to differ among the treatment groups (P = 0.074) with the least value in pigs fed the adipic acid diet. The concentrations of indole in slurry (P = 0.084) and isovalerate in feces (P = 0.062) tended to differ among the groups with the least values in the pigs fed the humic substance diet. In conclusion, benzoic acid supplemented has the potential to increase N utilization in pigs, and adipic acid supplemented to pig diets can decrease urinary pH and slurry pH. Although benzoic acid and adipic acid have limited effects in reducing odorous compounds, humic substances have potential to reduce some odorous compounds.

Interfacial hydrogen bond effect between CeO2 and g-C3N4 boosts conversion to adipic acid from aerobic oxidation of cyclohexane

The selective oxidation reaction of cyclohexane is one of the typical activated sp3 C-H reactions, and its product adipic acid (AA) is the indispensable raw material used to produce nylon. However, subjecting to the inertness of C-H bond and the great reactivity of AA, the targeted transformation of cyclohexane remains a challenge. Here, the interfacial hydrogen bond (IHD) was developed by anchoring CeO2 on graphite carbon nitride (g-C3N4) surface, which could boost targeted acquisition adipic acid from aerobic oxidation of cyclohexane. The results indicated that the IHD effect can be flexibly regulated by changing the ratio of Ce3+/Ce4+, further optimizing the properties of surface OH species and Lewis acid sites. Under the synergistic effect of Ce3+/Ce4+ and Lewis acid sites on reaction interface, the glorious performance (32.2% conversion of cyclohexane with 66.4% selectivity) was obtained over the as-prepared CeO2/g-C3N4 IHD system. In addition, the interfacial adsorption properties of cyclohexane were explored by the virtue of in situ infrared spectroscopy, revealing the IHD effect could tune the adsorption behavior of cyclohexanone and further improve the selectivity of AA. This work disclosed that engineering the interface hydrogen bond effect between CeO2 and g-C3N4 provided feasible strategies to obtain excellent catalyst for cyclohexane oxidation.

The effect of carbon chain length of cross-linking agent on the functionality of carrier- free immobilized Thermomyces lanuginosa lipase particles

The cross-linked enzyme (CLEs) of Thermomyces lanuginosa lipase (TLL) was prepared in an isocyanide-based multi-component reactions (ICMRs) platform by applying three di-acidic cross-linkers to unveil more factors contributing to the functional properties of CLEs. The linkers were 1,11-undecanedicarboxylic acid, azelaic acid, and adipic acid with 11, 7, and 4 carbon lengths, respectively, providing a proper tool to investigate the effect of linker length on the activity, stability, and selectivity of the resulting CLEs. The immobilization yields of 60–90 % and the specific activities of 168, 88.4 and 49 U/mg were obtained for the CLEs of 1,11-undecanedicarboxylic acid, azelaic acid, adipic acid, respectively. The lower activity of azelaic and adipic acid-mediated CLEs compared to the soluble TLL (110 U/mg) was explained by in silico calculations. The results revealed that as opposed to 1,11-undecanedicarboxylic acid, both linkers tended to penetrate the enzyme active site, thus resulting in a major inhibitory effect on the enzyme functionality. The thermal and co-solvent stability of the immobilized derivatives improved compared to those of free TLL. The selectivity of CLEs was also examined by catalytic release of main omega-3 fatty acids from fish oil, presenting the highest selectivity of 22 for the CLEs of azelaic acid.

A study on antibacterial and anti‐inflammatory activity of xylitol‐based polymeric nano‐bioactive glass nanocomposites

AbstractBioactive glasses have been shown effective in promoting bone healing by interacting with the body, gradual degradation, and supporting new bone growth. They present a promising option for therapies aimed at regenerating bone tissue. In this study, we developed a novel material, PXMA/n‐BG, by combining xylitol, maleic acid, and adipic acid, and incorporating nano‐bioactive glass, all synthesized without the use of a catalyst. The sol–gel method was used to fabricate the n‐BG (SiO2–CaO–P2O5). The incorporation of n‐BG into the polymer was found to enhance its biocompatibility and effectiveness for orthopedic applications. The synthesized polymer and its nanocomposite were characterized by FTIR, 1H NMR, 13C NMR, DSC, GPC, UTM, XRD and HR‐SEM. X‐ray diffraction and high‐resolution scanning electron microscopy are utilized to investigate the structure and surface of the n‐BG and polymeric composite material. The strength and flexibility of a plastic material with tiny particles mixed in were tested using a universal testing machine. We examined the elemental composition and thermal stability of n‐BG through specialized testing like energy‐dispersive X‐ray analysis (EDX) and thermogravimetric analysis (TGA). The research focused on the potential of xylitol‐based polymer and its nanocomposite to inhibit the growth of harmful bacteria in food. We conducted experiments to determine the efficacy of the antibacterial substance against various bacteria strains. The antibacterial potential of the extracts was assessed by the agar diffusion method using MHA plate. Furthermore, we investigated the ability of the material and its nanoparticles to reduce inflammation.