Polyvinyl Alcohol-sodium Alginate Research Articles

Preparation and Characterization of Amoxicillin-Loaded Polyvinyl Alcohol/Sodium Alginate Nanofibrous Mat: Drug Release Properties, Antibacterial Activity, and Cytotoxicity

AbstractThis study aimed to prepare a polyvinyl alcohol/sodium alginate (PVSA) nanofibrous mat as an amoxicillin (AMOX) delivery system. AMOX was loaded to the PVSA nanofibers during electrospinning, and the AMOX-loaded PVSA (PVSA/AMOX) nanofibrous mat was cross-linked by glutaraldehyde (GA). The PVSA/AMOX nanofibrous mat was characterized by Fourier Transform infrared spectroscopy, scanning electron microscopy, Brunauer–Emmett–Teller, and mercury porosimetry analyses. The thickness, air permeability, and water vapor transmission rate of the PVSA/AMOX nanofibrous mat were 0.43 ± 0.08 mm, 17.2 ± 4.91 L/m2/s, and 1485 ± 13.6 g/m2/d, respectively, which were suitable for wound dressing applications. The tensile strength was 6.73 ± 0.48 MPa and elongation at a maximum load was 81.9 ± 17.0%, within the ranges of human skin’s values. The total porosity was 59.4%, enabling cell adhesion, migration, and proliferation. The PVSA/AMOX nanofibrous mat has high swelling (319 ± 4.2%) and low degradation (2.2 ± 0.1% in 10 days) ratios. The nanofibrous mat cross-linked with 0.25% GA solution for 20 min had a 73.07% cumulative release for 90 min. The drug release kinetics were obeyed to the Korsmeyer-Peppas model. The nanofibrous mat presented antibacterial activity on S. aureus ATCC 29213 and E. coli ATCC 25922, and there was no cytotoxic effect on the human normal keratinocyte cells, demonstrating the potential for use in wound dressing applications.

A new strategy for accelerating recovery of anaerobic granular sludge after low-temperature shock: In situ regulation of quorum sensing microorganisms embedded in polyvinyl alcohol sodium alginate

Low-temperature could inhibit the performance of anaerobic granular sludge (AnGS). Quorum sensing (QS), as a communication mode between microorganisms, can effectively regulate AnGS. In this study, a kind of embedded particles (PVA/SA@Serratia) based on signal molecule secreting bacteria was prepared by microbial immobilization technology based on polyvinyl alcohol and sodium alginate to accelerate the recovery of AnGS system after low temperature. Low-temperature shock experiment verified the positive effect of PVA/SA@Serratia on restoring the COD removal rate and methanogenesis capacity of AnGS. Further analysis by metagenomics analysis showed that PVA/SA@Serratia stimulated higher QS activity and promoted the secretion of extracellular polymeric substance (EPS) in AnGS. The rapid construction of EPS protective layer effectively accelerated the establishment of a robust microbial community structure. PVA/SA@Serratia also enhanced multiple methanogenic pathways, including direct interspecies electron transfer. In conclusion, this study demonstrated that PVA/SA@Serratia could effectively strengthen AnGS after low-temperature shock.

Hesperidin - loaded PVA/alginate hydrogel: targeting NFκB/iNOS/COX-2/TNF-α inflammatory signaling pathway.

Skin injuries represent a prevalent form of physical trauma, necessitating effective therapeutic strategies to expedite the wound healing process. Hesperidin, a bioflavonoid naturally occurring in citrus fruits, exhibits a range of pharmacological attributes, including antimicrobial, antioxidant, anti-inflammatory, anticoagulant, and analgesic properties. The main objective of the study was to formulate a hydrogel with the intention of addressing skin conditions, particularly wound healing. This research introduces a methodology for the fabrication of a membrane composed of a Polyvinyl alcohol - Sodium Alginate (PVA/A) blend, along with the inclusion of an anti-inflammatory agent, Hesperidin (H), which exhibits promising wound healing capabilities. A uniform layer of a homogeneous solution comprising PVA/A was cast. The process of crosslinking and the enhancement of hydrogel characteristics were achieved through the application of gamma irradiation at a dosage of 30 kGy. The membrane was immersed in a Hesperidin (H) solution, facilitating the permeation and absorption of the drug. The resultant system is designed to deliver H in a controlled and sustained manner, which is crucial for promoting efficient wound healing. The obtained PVA/AH hydrogel was evaluated for cytotoxicity, antioxidant and free radical scavenging activities, anti-inflammatory and membrane stability effect. In addition, its action on oxidative stress, and inflammatory markers was evaluated on BJ-1 human normal skin cell line. We determined the effect of radical scavenging activity PVA/A (49 %) and PVA/AH (87%), the inhibition of Human red blood cell membrane hemolysis by PVA/AH (81.97 and 84.34 %), hypotonicity (83.68 and 76.48 %) and protein denaturation (83.17 and 85.8 %) as compared to 250 μg/ml diclofenac (Dic.) and aspirin (Asp.), respectively. Furthermore, gene expression analysis revealed an increased expression of genes associated with anti-oxidant and anti-inflammatory properties and downregulated TNFα, NFκB, iNOS, and COX2 by 67, 52, 58 and 60%, respectively, by PVA/AH hydrogel compared to LPS-stimulated BJ-1 cells. The advantages associated with Hesperidin can be ascribed to its antioxidant and anti-inflammatory attributes. The incorporation of Hesperidin into hydrogels offers promise for the development of a novel, secure, and efficient strategy for wound healing. This innovative approach holds potential as a solution for wound healing, capitalizing on the collaborative qualities of PVA/AH and gamma irradiation, which can be combined to establish a drug delivery platform for Hesperidin.

Enhancing nitrogen removal performance using immobilized aerobic denitrifying bacteria by modified polyvinyl alcohol/sodium alginate (PVA/SA)

Aerobic denitrification has emerged as a promising and efficient method for nitrogen removal from wastewater. However, the direct application of aerobic denitrifying bacteria has faced challenges such as low nitrogen removal efficiency, bacterial loss, and poor stability. To address these issues, this study developed a novel microbial particle carrier using NaHCO3-modified polyvinyl alcohol (PVA)/sodium alginate (SA) gel (NaHCO3-PVA/SA). This carrier exhibits several advantageous properties, including excellent mass transfer efficiency, favorable biocompatibility, convenient film formation, abundant biomass, and exceptional pollutant treatment capacity. The carrier was modified with 0.3% NaHCO3, 8.0% PVA, and 1.0% SA, resulting in a remarkable 3.4-fold increase in the average pore diameter and a 12.8% improvement in mass transfer efficiency. This carrier was utilized to immobilize the aerobic denitrifying bacterium Stutzerimonas stutzeri W-2 to enhance nitrogen removal (NaHCO3-PVA/SA@W-2), resulting in a NO3−-N removal efficiency of 99.06%, which was 21.39% higher than that without modification. Compared with the non-immobilized W-2, the degradation efficiency was improved by 43.70%. After five reuses, the NO3−-N and TN removal rates remained at 99% and 93.01%, respectively. These results provide a solid foundation for the industrial application of the modified carrier as an effective tool for nitrogen removal in large-scale wastewater treatment processes.

Enhanced treatment of acute organophosphorus pesticide poisoning using activated charcoal-embedded sodium alginate-polyvinyl alcohol hydrogel.

The adsorption of activated charcoal is currently a major clinical treatment for acute organophosphorus pesticide poisoning (AOPP). However, the adsorption duration and efficiency of this method is unstable. In this study, a hydrogel embedding activated charcoal was prepared and its alleviating effects on AOPP were investigated. A composite hydrogel using sodium alginate and polyvinyl alcohol (SA-PVA) hydrogel was prepared in this study. The structural properties of the SA-PVA hydrogel were characterized via multiple analysis including FTIR, TGA, XRD, SEM, tensile strength and expansion rate. Based on these, activated charcoal (AC) was embedded within the SA-PVA hydrogel (SA-PVA-AC) and it was used for the treatment of AOPP. Structural characterization indicated SA-PVA hydrogel possesses excellent mechanical properties and biocompatibility. The invivo study demonstrated that SA-PVA-AC significantly alleviated the inflammation and oxidative damage in the liver, as evidenced by reduced levels of IL-6, TNF-α, and, IL-1β, SOD, and MDA. Furthermore, SA-PVA-AC treatment effectively re-regulated the activities of serum AST and ALT, exhibiting an improved effect on liver function. The findings suggest that activated charcoal embedded within SA-PVA hydrogel has significant potential as a therapeutic agent in treating AOPP, and offering a novel approach to managing pesticide-induced toxicity.

Characterizations of Centrifugal Electrospun Polyvinyl Alcohol/Sodium Alginate/Tamanu Oil/Silver Nanoparticles Wound Dressing.

Known for its water solubility, flexibility, strong adhesion, and eco-friendly nature, polyvinyl alcohol (PVA) is widely used in various industries. In the medical field, it is used for applications such as creating bandages and orthopaedic devices. Incorporating sodium alginate (SA) into PVA membranes enhances their structural integrity, breathability, and permeability, thereby minimising the risk of cellular damage in the wound zone. Moreover, the addition of tamanu oil (C alophyllum inophyllum L.) and silver nanoparticles, both of which are known for their antibacterial properties and benefits in traditional wound healing, further enhances the membranes' wound-healing effectiveness. Following production, the membranes undergo a series of tests designed to evaluate their physical properties as well as their antioxidant and antibacterial capabilities. Subsequently, in vitro testing is conducted using human skin cells; experiments on Wistar rats are then performed. Numerous experiments have consistently demonstrated that the performance of polyvinyl alcohol/sodium alginate/tamanu oil (PVA/SA/Oil) membrane is superior to that of polyvinyl alcohol/sodium alginate/tamanu oil/silver nanoparticles (PVA/SA/Oil/Ag NP) membrane. Specifically, the polyvinyl alcohol/sodium alginate (PVA/SA) combination exhibits an impressive wound-healing rate of 98.82% after 15 days, with cells maintaining a high viability of 92% in a nourishing environment. Moreover, these membranes exhibit exceptional resistance to the oxidation of free radicals, surpassing the 70% threshold, and they possess antibacterial activity against Staphylococcus aureus subsp. aureus in vitro. Based on the obtained results, the nanofiber membranes composed of polyvinyl alcohol/ alginate/ tamanu oil, with or without silver nanoparticles, have shown potential as wound dressings in the wound care discipline.

Invasive plant-derived biochar for sustainable bioremediation of pesticide contaminated soil

Managing invasive plant presents a significant challenge to both the environment and the economy. There is an opportunity to address this issue by utilizing invasive plants as a sustainable and cost-effective source of valuable functional materials for environmental remediation. In this study, a promising Mikania micrantha biochar (MB) was synthesized by pyrolyzing an invasive plant, which was utilized for bacterial immobilization and adsorption of contaminants. By embedding Proteus terrae ZQ02-MB within a polyvinyl alcohol-sodium alginate gel to create a biochar-modified bacterial microsphere (BBM), the superior degradation of pesticide contaminants was observed. Taking chlorothalonil (CHT) as an example, field experiments demonstrated that BBM achieved a removal efficiency of 59.8% by the third day. Additionally, BBM not only improved the richness and diversity of soil bacteria but also enhanced the microbial community structure by the seventh day. On this basis, the adsorption capacity of MB, biofilm growth promoting ability of BBM, and the CHT mineralization ability of strain ZQ02 were validated as a joint mechanism to promote efficient CHT removal. Overall, this study proposes a composite model of invasive plant-derived biochar loaded microorganisms, which has great potential in eliminating pollutant residues and paves new paths to develop strategies for reusing invasive species resources.

Evaluating the Volume Ratio Effect on Absorption Time of Polyvinyl Alcohol-Sodium Alginate Based Fiber Membranes as a Wound Dressing

This research was observed absorption of the membrane PVA/SA fiber as wound dressing. The electrospinning method is used to make fiber membranes. This method with a volume ratio composition of Polyvinyl Alcohol (PVA) - sodium alginate (SA) (PVA/ SA) of 9 :1 (v/v), 8:2 (v/v), and 7:3 (v/v). The PVA/SA membrane was characterized with absorption characterization-water absorption test, morphology and fiber diameter. Absorption characterization-water absorption test results that the fastest absorption time occurred on the PVA/SA fiber membrane with a ratio of 7:3 (v/v). From the SEM results, it is known that the morphology of the PVA/SA membrane shows a fiber size with a uniform diameter. The fiber diameter decreases as it increases SA volume fraction. Fibers with a small diameter will have a large surface area and absorb liquid more quickly. Keywords: electrospinning, wound dressing, absorption characterization-water absorption test, size fiber

Continuous monitoring of temperature and freshness in cold chain transport based on the dual-responsive fluorescent hydrogel

Comprehensive attention should be paid to the potential food spoilage in food transport. However, there is a problem of freshness destruction by repeated freezing and thawing during the cold chain transport. Herein, a fluorescent hydrogel with N-doped green-emitting carbon dots (N-GCDs), bovine serum albumin-gold nanoclusters (BSA-AuNCs) as fluorescent probes and polyvinyl alcohol-sodium alginate hydrogel as carrier matrix was developed to continuously detect temperature and freshness. Due to the solvatochromic effect of N-GCDs, when the temperature surpassed the threshold, the mixture of water and dimethyl sulfoxide underwent a phase transition and melted into the gel, changing the fluorescence color to realize the temperature monitoring. Then, due to the pH effect of BSA-AuNCs, the gel could respond to pH changes in food deterioration to monitor the food freshness. Thus, the changes of both fluorescence color and intensity of the hydrogel provides a new method for visual and portable authenticity of food freshness.

Molybdenum disulfide nanoflowers - doped sodium alginate/polyvinyl alcohol porous xerogel for methylene blue and copper ion adsorption

In order to improve the adsorption performance of MoS2, as well as to solve the problems of MoS2-powder in adsorption, which is prone to agglomeration and difficulty to be recycled, we prepared MoS2-nanoflowers(MoS2-NFs), and mixed them with sodium alginate/polyvinyl alcohol(SA/PVA) to prepare MoS2-NFs/SA/PVA xerogel(MSP) by freezing-lyophilization. Then two forms of xerogels - block-MSP(MSPB) and spherical-MSP(MSPS) were prepared, and they were used as methylene blue(MB) and Cu2+ adsorbent. It was found that MoS2-NFs were evenly dispersed inside the SA/PVA with no agglomeration, while the interior of MSPB/MSPS showed the structure of parallel-pores and radial-pores, respectively. The adsorption capacity of MSPB/MSPS on MB can reach 233 mg/g, which is five times higher than SA/PVA-gel, showing excellent synergistic-adsorption effect, and the adsorption capacity for Cu2+ reaches 271 mg/g. The adsorption mechanism indicated that the adsorption of MB by MSPB/MSPS conformed to pseudo-first-order model, with electrostatic force as the main force. And their adsorption of Cu2+ conformed to pseudo-second-order model and was dominated by Lewis acid/base soft-soft interactions. Notably, after long-term adsorption, MSPB/MSPS maintains its shape and more than 90 % of the adsorption capacity, ensuring the recovery and reuse of materials. So, MSPB/MSPS has great potential in adsorption, providing a new solution for sewage purification.

Investigation on polyvinyl alcohol and sodium alginate blend matrix with ammonium nitrate conducting electrolytes for electrochemical applications

Polyvinyl alcohol (PVA) Sodium alginate (NaAlg) polymer composites were synthesized by solution casting technique and doping with ammonium nitrate (NH4NO3). The functionalization structure of the produced electrolytes was investigated using XRD and AC impedance spectroscopy. XRD confirms amorphous nature. The ionic conductivity of the electrolytes is evaluated using ac impedance measurements at temperatures ranging from 303 to 353 K. PVA: NaAlg: NH4NO3 (60:40:15 wt%) blend polymer electrolyte was observed to have the highest conductivity of 1.05 × 10−6 S cm−1. The Arrhenius plot appears to be obeyed by the temperature dependent ionic conductivity and is of non-debye type. Activation energy for best conducting electrolyte was 0.2364 eV. The dielectric relaxation of the polymer electrolyte has been studied, and the results are described. Relaxation time estimated from loss tangent analysis also affirms that value is low for highest conducting sample. Results of CV and LSV studies gave a plausible approach for electrochemical application.

A Novel Method for γ-Aminobutyric Acid Biosynthesis Using Glutamate Decarboxylase Entrapped in Polyvinyl Alcohol-Sodium Alginate Capsules.

γ-aminobutyric acid (GABA) has essential physiological functions in the human body. A novel method using glutamate decarboxylase (GAD) entrapped in polyvinyl alcohol (PVA)-sodium alginate (SA) capsules provides a green biological strategy for GABA synthesis. In this investigation, the stability range of immobilized GAD was effectively broadened, and immobilized GAD could be repeatedly used as a batch and fixed-bed column catalyst. The immobilized enzymes were stable and retained 89% of their activity in a pH range of 4.0-5.6, while there was an approximately 50% decrease in free GAD activity in the pH range of 4.8 ± 0.4. The immobilized GAD affinity to the substrate improved, and this was evidenced by the apparent decrease in Km to 13.3 mmol/L from the 30.9 mmol/L for free GAD. The immobilized GAD retained >90.6% activity after eight cycles and a near-100% enzyme activity retention after 120 h of a continuous fixed-bed column catalyst operation. This study has thus presented an effective PVA-SA-GAD immobilization method that could be used to continuously scale-up GABA biosynthesis.

Effects of released organic components of solid carbon sources on denitrification performance and the related mechanism

Here, a hybrid scaffold of polyvinyl alcohol/sodium alginate (PVA/SA) was used to prepare solid carbon sources (SCSs) for treating low carbon/nitrogen wastewater. The four SCSs were divided into two groups, biodegradable polymers group (including polyvinyl alcohol-sodium alginate (PS) and PS-PHBV (PP), and blended SCSs (PS-PHBV-wood chips (PPW) and PS-PHBV-wheat straw (PPS)). After the leaching experiments, no changes occurred in elemental composition and functional groups of the SCSs, and the released dissolved organic matter showed a lower degree of humification and higher content of labile molecules in the blended SCSs groups using EEM and FT-ICR-MS. The denitrification performance of the blended SCSs was higher, with nitrate removal efficiency over 84%. High-throughput sequencing confirmed PPW had the highest alpha-diversity, and the microbial community structure significantly varied among SCSs. Results of functional enzymes and genes show the released carbon components directly affect the NADH level and electron transfer efficiency, ultimately influencing denitrification performance.

Insight into the microbial community of denitrification process using different solid carbon sources: Not only bacteria

There is a lack of understanding about the bacterial, fungal and archaeal communities’ composition of solid-phase denitrification (SPD) systems. We investigated four SPD systems with different carbon sources by analyzing microbial gene sequences based on operational taxonomic unit (OTU) and amplicon sequence variant (ASV). The results showed that the corncob-polyvinyl alcohol sodium alginate-polycaprolactone (CPSP, 0.86±0.04 mg NO3−-N/(g·day)) and corncob (0.85±0.06 mg NO3−-N/(g·day)) had better denitrification efficiency than polycaprolactone (PCL, 0.29±0.11 mg NO3−-N/(g·day)) and polyvinyl alcohol-sodium alginate (PVA-SA, 0.24±0.07 mg NO3−-N/(g·day)). The bacterial, fungal and archaeal microbial composition was significantly different among carbon source types such as Proteobacteria in PCL (OTU: 83.72%, ASV: 82.49%) and Rozellomycota in PVA-SA (OTU: 71.99%, ASV: 81.30%). ASV methods can read more microbial units than that of OTU and exhibit higher alpha diversity and classify some species that had not been identified by OTU such as Nanoarchaeota phylum, unclassified_ f_ Xanthobacteraceae genus, etc., indicating ASV may be more conducive to understand SPD microbial communities. The co-occurring network showed some correlation between the bacteria fungi and archaea species, indicating different species may collaborate in SPD systems. Similar KEGG function prediction results were obtained in two bioinformatic methods generally and some fungi and archaea functions should not be ignored in SPD systems. These results may be beneficial for understanding microbial communities in SPD systems.

Biochar/Clay Composite Particle Immobilized Compound Bacteria: Preparation, Collaborative Degradation Performance and Environmental Tolerance

Immobilized microbial materials can effectively remove pollutants from surface water, and a biochar/clay composite particle (BCCP) material is prepared with immobilized Flavobacterium mizutaii sp. and Aquamicrobium sp. to remove ammonia nitrogen (NH4+–N) and petroleum hydrocarbons (PHCs). The results indicated that the optimal ratios of biochar, Na2SiO3 and NaHCO3 were 15%, 3%, and 3%, and the adsorption process was found to be better described with the pseudo-second-order kinetic equation. The individual immobilization of Flavobacterium mizutaii sp. and Aquamicrobium sp. with sodium alginate–polyvinyl alcohol (PVA + SA) achieved 80% and 90% removal efficiencies for NH4+–N and PHCs at the 10th d. The composite immobilization of two efficient bacteria could degrade 82.48% NH4+–N and 74.62% PHCs. In addition, immobilization relieved the effects of temperature and salinity. This study can provide guidance for the application of immobilized microbial composite materials in natural water environments.

Preparation of hydroxyapatite nanofibers by using ionic liquids as template and application in enhancing hydrogel performance.

Introduction: Hydroxyapatite (HAP or HA) nanofibers are very attractive in the field of biomedical engineering. However, templates used for preparing HAP nanofibers are usually hydrophobic molecules, like fatty acids and/or surfactants, which are difficult to remove and potentially toxic. Therefore, it is important to develop a green approach to prepare HAP nanofibers. Methods: Imidazolium-based ionic liquids (ILs) were used as templates to control the crystallization of HAP. The obtained HAP nanofibers were composited into polyvinyl alcohol-sodium alginate (PVA-Alg) hydrogel (HAP@H). The rheological performance, stretching, and compression properties were tested. Scanning electron microscope (SEM), high resolution transmission electron microscope (HRTEM), X-ray diffraction (XRD), Fourier-transform infrared (FT-IR), and differential scanning calorimetry (DSC) were adopted to characterize the morphology, size, crystallographic orientations, and phase of HAP@H. Results: HAP nanofibers with a length of ∼50μm were harvested. The DSC results proved that water loss temperature increased from 98°C (for pure hydrogel) to 107°C (for HAP@H). Also, HAP@H hydrogel presented much better porous structure, tensile performance, and compressive performance than that of pure hydrogel. Discussion: The morphology, size, and growth direction of HAP could be modulated easily by altering the alkyl chain length of ILs' cations. This is possibly due to face-specific adsorption of imidazolium moieties on HAP nanocrystals. The enhancing performance of HAP@H is probably due to the composited highly oriented HAP nanofibers.

Linear and Nonlinear Optical Properties of PVA:SA Blend Reinforced by TiO2 Nanoparticles Prepared by Flower Extract of Aloe Vera for Optoelectronic Applications

In this study, a polyvinyl alcohol–sodium alginate blend, PVA:SA 3:1 (w:w), was doped with different contents of TiO2 nanoparticles (NPs) prepared by aloe vera leaf extract to form the investigated nanocomposites. The nonlinear parameters of third-order susceptibility (χ(3)) and refractive index (n2) were detected by using UV-Vis spectroscopy and Z-scan techniques. Some different optical parameters were also determined, including the refractive index (n), optical dielectric parameters, volume and surface energy loss functions, and some others. The best solar skin protection factor (SSPF) was investigated by 5 wt.% of TiO2 NPs doped in PVA:SA 3:1, which was about 84.6% compared to the corresponding value of the host blend (41%). The studied nanocomposites were examined for their utility in the optical limiting of CUT-OFF laser filters utilizing a continuous He-Ne laser working at 632.2 nm. As a result, our finding demonstrated that TiO2 NPs doped in the host blend of PVA:SA positively influences a laser light blocking for the investigated laser source. Using the estimated gap energies values, different models were used to deduce theoretical values of the linear refractive index (n). The presence of Ti peaks in the EDX spectrum confirmed the doping of TiO2 NPs in the nanocomposites. SEM showed that the TiO2 NPs are homogeneously dispersed through the host blend with some agglomerates. XRD spectra showed that the values of the lattice strain εstr. detected at 2ϴ = 19.78° are 0.058, 0.055, and 0.060, corresponding to 1, 3, and 5 wt.% of TiO2 NPs doped in the PVA:SA blend.

Fabrication of Glutaraldehyde Vapor Treated PVA/SA/GO/ZnO Electrospun Nanofibers with High Liquid Absorbability for Antimicrobial of Staphylococcus aureus.

In this study, we aim to develop organic-inorganic hybrid nanofibers containing high moisture retention and good mechanical performance as an antimicrobial dressing platform. The main theme of this work focuses on several technical tasks including (a) the electrospinning process (ESP) to produce organic polyvinyl alcohol/sodium alginate (PVA/SA) nanofibers with an excellent diameter uniformity and fibrous orientation, (b) the fabrication of inorganic nanoparticles (NPs) as graphene oxide (GO) and ZnO NPs to be added to PVA/SA nanofibers for enhancement of the mechanical properties and an antibacterial function to Staphylococcus aureus (S. aureus), and then (c) the crosslinking process for PVA/SA/GO/ZnO hybrid nanofibers in glutaraldehyde (GA) vapor atmosphere to improve the hydrophilicity and moisture absorption of specimens. Our results clearly indicate that the uniformity nanofiber with 7 wt% PVA and 2 wt% SA condition demonstrates 199 ± 22 nm in diameter using an electrospinning precursor solution of 355 cP in viscosity by the ESP process. Moreover, the mechanical strength of nanofibers was enhanced by 17% after the handling of a 0.5 wt% GO nanoparticles addition. Significantly, the morphology and size of ZnO NPs can be affected by NaOH concentration, where 1 M NaOH was used in the synthesis of 23 nm ZnO NPs corresponding to effective inhibition of S. aureus strains. The PVA/SA/GO/ZnO mixture successfully performed an antibacterial ability with an 8 mm inhibition zone in S. aureus strains. Furthermore, the GA vapor as a crosslinking agent acting on PVA/SA/GO/ZnO nanofiber provided both swelling behavior and structural stability performance. The swelling ratio increased up to 1.406%, and the mechanical strength was 1.87 MPa after 48 h of GA vapor treatment. Finally, we successfully synthesized the hybrid nanofibers of GA-treated PVA/SA/GO/ZnO accompanied with high moisturizing, biocompatibility, and great mechanical properties, which will be a novel multi-functional candidate for wound dressing composites for patients receiving surgical operations and first aid treatments.

Enhanced remediation of phenanthrene in water and soil by novel biochar-immobilized bacterial microspheres

Bioaugmentation is often considered a promising technology for the removal of polycyclic aromatic hydrocarbons; however, available high-efficiency microbial agents remain very limited. In this study, the green solvent polyethylene glycol 200 and Fe (NO3)3·9H2O were introduced to prepare iron-modified biochar materials by one-step pyrolysis. This material had a specific surface area of 407 m2⋅g−1 and high microbial immobilization efficiency. The addition of polyethylene glycol 200 promoted hydrolysis of iron ions, improved the surface structure and roughness of the biochar material, and promoted attachment of microorganisms on its surface. Using a polyvinyl alcohol–sodium alginate–iron-modified biochar composite, Pseudomonas aeruginosa bacteria were fixed by boric acid–CaCl2 cross-linking to remove phenanthrene from aqueous solution and soil. The results showed that the iron-modified biochar microorganism spheres could completely degrade 20 mg·L−1 of phenanthrene in solution within 12 h; degradation efficiency of 80 mg·L−1 phenanthrene was 50%. In the soil system, the modified biochar spheres had higher degradation performance compared with P. aeruginosa alone, reaching a removal efficiency of 30% in 6 d. This study provides a strategy for the effective treatment of organic pollutants in harsh environments by coupling the efficient adsorption of green materials with the biodegradability of microorganisms.

Enhancing mechanical properties of polyvinyl alcohol/sodium alginate gel beads by graphene oxide for the aerobic sludge immobilization in wastewater treatment

This study reinforced polyvinyl alcohol/sodium alginate (PVA/SA) gel beads immobilizing aerobic sludge with graphene oxide (GO) as a nanofiller. The different types of beads were made by various concentrations of GO (0.02, 0.2, 2, 20, and 200 mg/L). The effect of GO on beads structure was observed by comparing the mechanical properties of chemical oxygen demand (COD) and NH<sub>4</sub><sup>+</sup>-N removal efficiencies. The results showed that the PVA/SA/GO gel carriers have excellent reinforcement properties compared to non-GO gel carriers, while sphericity factor and methylene blue absorption are the same. The strongest carrier contains 200 mg/L GO, referred to as GO6. In addition, the highest COD and NH<sub>4</sub><sup>+</sup>-N removal efficiencies of GO6 gel carriers were 97 and 96.67%, respectively, which is higher than a non-GO PVA/SA (GO1) gel carrier. The addition of GO (200 mg/L) was thus an effective way to improve the mechanical strength of PVA/SA gel beads due to the strong interaction between GO and the PVA/SA matrix. It can also promote COD and NH<sub>4</sub><sup>+</sup>-N removal efficiency of immobilized bacteria inside the beads.