Facile fabrication and characterization of high-performance Borax-PVA hydrogel
Source abstract
Abstract
Borax-PVA hydrogels with excellent mechanical properties are prepared by simple physical mixing of polyvinyl alcohol (PVA, thickener) and borax (cross-linking agent) at room temperature. The resulting hydrogel is a three-dimensional structure composed of boric ester bonds as physical crosslinking points. Thus, the spatial structure, swelling properties, viscoelastic properties, tensile properties, and self-healing properties of hydrogels with different ratios of borax and PVA are studied. XRD confirmed that the hydrogels have similar structures near 2θ values of 10 and 20. The microstructure of the hydrogel is confirmed by SEM and TEM. With an increase of borax mass fraction, the pore structure and morphology of hydrogel are more ordered, with substantial quantities of water immobilized within their three-dimensional structure. The viscoelastic properties and tensile properties showed that when the mass fraction of borax is 5%, the storage modulus and compressive stress of the hydrogel are the highest, reaching 100 Pa and 5.6 kPa, respectively. In addition, through physical and chemical stimulation (heating and varying pH, respectively), the hydrogels also showed reversible gel–sol conversion characteristics, indicating that the boric ester bonds have self-healing properties.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Hydrogels: synthesis, properties, applications · Electrospun Nanofibers in Biomedical Applications · Advanced Sensor and Energy Harvesting Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (31)
Show source-provided references
1. Liu L, Pan G, Wang L (2018) Hybrid hydrogels toughened by chemical covalent bonding and physical electrostatic interactions. Chem Res Chin Univ 34:500–50510.1007/s40242-018-7375-z ↗
2. Dai WS, Barbari TA (2000) Gel-impregnated pore membranes with mesh-size asymmetry for biohybrid artificial organs. Biomaterials 21:1363–137110.1016/S0142-9612(00)00022-3 ↗
3. Gao L, Zhang H, Yu B (2020) Chitosan composite hydrogels cross-linked by multifunctional diazo resin as antibacterial dressings for improved wound healing. J Biomed Mater Res Part A 108:1890–189810.1002/jbm.a.36952 ↗
4. Driest PJ, Allijn IE, Dijkstra DJ (2020) Poly(ethylene glycol)-based poly(urethane isocyanurate) hydrogels for contact lens applications. Polym Int 69:131–13910.1002/pi.5938 ↗
5. LimaSousa R, de MeloDiogo D, Alves CG (2020) Injectable in situ forming thermo-responsive graphene based hydrogels for cancer chemo-photothermal therapy and NIR light-enhanced antibacterial applications. Mater Sci Eng C 117:111294–11129410.1016/j.msec.2020.111294 ↗
6. Li Q, Ning Z, Ren J (2018) Structural design and physicochemical foundations of hydrogels for biomedical applications. Curr Medicinal Chem 25:963–98110.2174/0929867324666170818111630 ↗
7. Chocholata P, Kulda V, Dvorakova J (2020) Biological evaluation of polyvinyl alcohol hydrogels enriched by hyaluronic acid and hydroxyapatite. Int J Mol Sci 21:325–33510.3390/ijms21165719 ↗
8. Ding F, Li H, Shi X (2020) Electrodeposition of polysaccharide and protein hydrogels for biomedical applications. Curr Medicinal Chem 27:2610–263010.2174/0929867326666190405151538 ↗
9. Fathi-Achachelouei M, Keskin D, Bat E (2020) Dual growth factor delivery using PLGA nanoparticles in silk fibroin/PEGDMA hydrogels for articular cartilage tissue engineering. J Biomed Mater Res Part B 108:2041–206210.1002/jbm.b.34544 ↗
10. Damiano M, Virginia M, Roberto M (2019) Chemical characterization of hydrogels crosslinked with polyethylene glycol for soft tissue augmentation. Macedonian J Med Sci 7:1077–1081
11. Xiaomin H, Dong Z, Jiahui W (2019) One-pot and one-step fabrication of salt-responsive bilayer hydrogels with 2D and 3D shape transformations. ACS Appl Mater interfaces 11:25417–2542610.1021/acsami.9b06691 ↗
12. Shanmugapriya K, Kim H, Lee YW (2020) Multifunctional heteropolysaccharide hydrogel under photobiomodulation for accelerated wound regeneration. Ceram Int 46:7268–727810.1016/j.ceramint.2019.11.221 ↗
13. Mohammadian M, Salami M, Emam-Djomeh Z (2019) Characterization of hydrogels formed by non-toxic chemical cross-linking of mixed nanofibrillated/heat-denatured when proteins. J Iran Chem Soc 16:2731–274110.1007/s13738-019-01733-z ↗
14. Mallick, Singh S (2020) Strategies toward development of biodegradable hydrogels for biomedical applications. Polym-Plast Technol Mater 59:911–927
15. Zhang J, Liu T, Liu Z, Wang Q (2019) Facile fabrication of tough photocrosslinked polyvinyl alcohol hydrogels with cellulose nanofibrils reinforcement. Polymer 173:103–10910.1016/j.polymer.2019.04.028 ↗
16. Wang Y, Xue Y, Wang J, Zhu Y, Zhang X, Liao J, Li X, Wu X, Qin Y, Chen WA (2019) Composite hydrogel with high mechanical strength fluorescence and degradable behavior for bone tissue engineering. Polymers 11:1112–112310.3390/polym11071112 ↗
17. Fangchao C, Jiadi S, Jian J et al. (2020) Carbon dots-releasing hydrogels with antibacterial activity, high biocompatibility, and fluorescence performance as candidate materials for wound healing. J Hazard Mater 23:330–340
18. Oveissi F, Naficy S, Le TYL et al. (2019) Tough hydrophilic polyurethane-based hydrogels with mechanical properties similar to human soft tissues. J Mater Chem B 7:3512–351910.1039/C9TB00080A ↗
19. Yao H-Y, Lin H-R, Sue G-P et al. (2019) Chitosan-based hydrogels prepared by UV polymerization for wound dressing. Polym Polym Compos 27:155–16710.1177/0967391118820477 ↗
20. Asghar S, Minhas MU, Ahmad M et al. (2018) Hydrophobic-hydrophilic cross-linked matrices for controlled release formulation of highly water-soluble drug venlafaxine: synthesis and evaluation studies. Adv Polym Technol 37:3146–315810.1002/adv.22085 ↗
21. Işikver Y, Saraydin D (2019) Stimuli responsive hydrogels: NIPAM/AAm/carboxylic acid polymers. Acta Chem Iasi 27:155–18410.2478/achi-2019-0012 ↗
22. Paulo F, Santos L (2019) Microencapsulation of caffeic acid and its release using a W/O/W double emulsion method: assessment of formulation parameters. Dry Technol 37:950–96110.1080/07373937.2018.1480493 ↗
23. Tran TD, Ogbourne SM, Brooks PR (2020) Lessons from exploring chemical space and chemical diversity of propolis components. Int J Mol Sci 21:568–57910.3390/ijms21020568 ↗
24. Ceylan S, Göktürk D, Bölgen N (2016) Effect of crosslinking methods on the structure and biocompatibility of polyvinyl alcohol/gelatin cryogels. Bio-Med Mater Eng 27:327–34010.3233/BME-161589 ↗
25. Enxiang L, Hongwei Z, Xiaobin D (2013) Fabrication of a rhythmic assembly system based on reversible formation of dynamic covalent bonds in a chemical oscillator. Chem Commun 49:5384–538610.1039/c3cc42533a ↗
26. Sun Z, Wang L, Jiang X (2020) Self-healing, sensitive and antifreezing biomass nanocomposite hydrogels based on hydroxypropyl guar gum and application in flexible sensors. Int J Biol Macromolecules 155:1569–157710.1016/j.ijbiomac.2019.11.134 ↗
27. Zhang, Ding, Feng et al. (2017) Synthesis and characterization of poly(N-isopropylacrylamide)/graphene oxide nanocomposite hydrogels by using glow discharge electrolysis plasma. Soft Mater 15:73–8110.1080/1539445X.2016.1249801 ↗
28. Kollár J, Mrlík M, Moravčíková D et al. (2019) Effect of monomer content and external stimuli on properties of renewable Tulipalin A-based superabsorbent hydrogels. Eur Polym J 115:99–10610.1016/j.eurpolymj.2019.03.012 ↗
29. Zhang J, Liu J (2011) Synthesis and characterization of a new thermosetting boric acid ester. Adv Mater Res 1268:1907–191010.4028/www.scientific.net/AMR.239-242.1907 ↗
30. Lee ML, Kim SH, Kim SJ (1996) Preparation and characteristics of β-chitin and poly(vinyl alcohol) blend. Polymer 37:5897–590510.1016/S0032-3861(96)00449-1 ↗
31. Assender HE, Windle AH (1998) Crystallinity in poly(vinyl alcohol) 2. Computer modelling of crystal structure over a range of tacticities. Polymer 39:4303–431210.1016/S0032-3861(97)10297-X ↗