مروری بر اسیدهای زیست‌پایه در تولید هیدروژل‌های پلیمر اَبَرجاذب هیبریدی

نوع مقاله : مروری

نویسندگان

1 زنجان دانشگاه زنجان، دانشکده علوم ، گروه شیمی، کد پستی 38791-45371

2 تهران، پژوهشگاه پلیمر و پتروشیمی ایران، صندوق پستی 112-14975

3 زنجان، دانشگاه زنجان، پژوهشکده فناوری‌های نوین زیستی، گروه زیست‌فناوری، کد پستی 38791-45371

چکیده

در سال‌های اخیر، هیدروژل‌ها به‌دلیل داشتن خواص منحصر به‌فرد، به‌عنوان یکی از امیدبخش‌ترین مواد درنظر گرفته شده‌اند. هیدروژل‌ها ساختارهای پلیمری آب‌دوست شبکه‌ای‌شده هستند که قابلیت جذب و نگه‌داری آب یا سیال‌های زیستی را دارند. بنابراین، شبکه‌های هیدروژلی به‌طور گسترده در محیط‌های آبی بدون حل‌شدن، متورم می‌شوند. هیدروژل‌ها در چند دهه گذشته در صنایع مختلف نظیر غذایی، بسته‌بندی، داروسازی و سامانه‌های دارورسانی، کشاورزی، کاربردهای زیست‌پزشکی و زیست‌مهندسی، ساخت دستگاه‌های فنی و الکترونیکی و نیز به‌عنوان جاذب برای حذف آلاینده‌ها در کاربردهای زیست‌محیطی به‌کار گرفته شده‌اند. هیدروژل‌های اَبَرجاذب  نوعی از هیدروژل‌ها هستند که به‌دلیل ماهیت آب‌دوست زنجیرهای پلیمری، قابلیت جذب و نگه‌داری مقدار زیادی آب یا محلول‌های آبی را تا صدها برابر وزن خود دارند. در سال‌های اخیر،  هیدروژل‌های ابرجاذب جدید برای کاربردهای مختلف توسعه یافته‌اند. تقاضای زیاد برای این مواد به‌ویژه در مصارف بهداشت فردی، رشد روزافزون تولید آن‌ها را موجب شده ‌است (اکنون بیش از بر سه میلیون تُن در سال). از آنجا که اجزای اصلی سازنده ابرجاذب‌های تجاری و پرکاربرد در صنعت، بر پایه مواد اولیه‌ حاصل از منابع فسیلی (نفت، گاز و زغال‌سنگ) است، بنابراین کاربرد گسترده ابرجاذب‌ها و افزایش تولید آن‌ها از یک سو با سهیم‌شدن در آلودگی آب، خاک و هوا موجب بروز نگرانی‌های زیست‌محیطی شده و از سوی دیگر، با تهدید نوسان‌های قیمت جهانی و تخریب‌پذیری منابع فسیلی مواجه شده است. از این‌رو، جایگزینی برخی از اجزای ابرجاذب‌ها با مواد اولیه پایه‌طبیعی، زیست‌پایه یا تجدیدپذیر (مانند لاکتیک اسید، سوکسینیک اسید و ایتاکونیک اسید) و تولید ابرجاذب‌های با ساختارهای هیبریدی مورد توجه قرار گرفته ‌است. هدف این مقاله مرور ابرجاذب‌های هیبریدی بر پایه برخی ترکیبات زیست‌پایه است که در سه بخش ساختاری شبکه پلیمری شامل شبکه‌ای‌کننده، اصلاح‌کننده سطح و مونومر به‌کار گرفته می‌شوند. 

کلیدواژه‌ها

عنوان مقاله [English]

Biobased Acids in Production of Hybrid Superabsorbent Polymer Hydrogels: A Review

نویسندگان [English]

  • Alaleh Dabbaghi 1
  • Hajar Jamshidi 2
  • Mohammad Jalal Zohuriaan-Mehr 2
  • Kourosh Kabiri 2
  • Ali Ramazani 3
1 Department of Chemistry, Faculty of Science, University of Zanjan, Postal Code 45371-38791, Zanjan, Iran
2 Iran Polymer and Petrochemical Institute, P.O. Box 14975-112
3 Department of Biotechnology, Research Institute of Modern Biological Techniques, University of Zanjan, Postal Code 45371-38791, Zanjan, Iran
چکیده [English]

In recent years, hydrogels have been considered as one of the mos‌t promising materials due to their unique properties. Hydrogels are cross-linked hydrophilic polymer s‌tructures that are able to absorb and holding water or biological fluid. Thus, the hydrogel networks can extensively swell in water media without dissolution. In the las‌t few decades, hydrogels been used in various indus‌tries such as food, packaging, pharmaceuticals and drug delivery sys‌tems, agriculture, biomedical and bioengineering applications, manufacturing of technical and electronic devices, and as adsorbents for the removal of pollutants in environmental applications. Superabsorbent polymer (SAP) hydrogels are a type of hydrogel that, due to the hydrophilic nature of polymer chains can absorb and retain extraordinary large amounts of water or aqueous solution up to hundreds of times their weight. In recent years, , new superabsorbent hydrogels have been developed for different applications. High demand for these subs‌tances, especially in personal hygiene, has led to an increase in their production (now over three million tons per year). Because the main components of commercial and widely used SAPs in indus‌try are based on raw materials derived from fossil resources (oil, gas and coal), the widespread use of SAPs and their increasing production, on the one hand, have contributed to environmental concerns by contributing to water, soil and air pollution, and, on the other hand, have threatened global price fluctuations and the degradability of fossil resources. Therefore, the replacement of at leas‌t some components of SAPs with natural, biobased or renewable raw materials (such as lactic acid, succinic acid and itaconic acid) and the production of SAPs with hybrid s‌tructures have been considered. The purpose of this paper is to review the hybrid SAPs based on some biobased compounds that are used in three s‌tructural parts of the polymer network including crosslinker, surface modifier and monomer. 

کلیدواژه‌ها [English]

  • superabsorbent hydrogel
  • biobased
  • cross-linking
  • surface modification
  • swelling

مراجع

  1. Ulber R., Muffler K., Tippkötter N., Hirth T., and Sell D., Introduction to Renewable Resources in the Chemical Indus‌t‌ry, Renewable Raw Materials: New Feeds‌t‌ocks for the Chemical Indus‌t‌ry, 1-5, 2011.
  2. Haq M., Burgueño R., Mohanty A.K., and Misra M., Hybrid Bio-based Composites from Blends of Unsaturated Polyes‌t‌er and Soybean Oil Reinforced with Nanoclay and Natural Fibers, Compos. Sci. Technol., 68, 3344-3351, 2008.
  3. Wool R. and Sun X.S., Bio-based Polymers and Composites, Elsevier, 2011.
  4. Fu J., Hydrogel Properties and Applications, J. Mater. Chem. B, 7,1523-1525, 2019.
  5. Zohuriaan-Mehr M.J. and Kabiri K., Superabsorbent Polymer Materials: A Review, Iran. Polym. J., 17, 451-477, 2008.
  6. Patiño-Masó J., Serra-Parareda F., Tarrés Q., Mutjé P., Espinach F.X., and Delgado-Aguilar M., TEMPO-Oxidized Cellulose Nanofibers: A Potential Bio-based Superabsorbent for Diaper Production, Nanomaterials, 9 , 1271, 2019.
  7. Jamshidi H., A Review on Hydrogels: Types, Synthesis Methods and Applications, Iran Polym. Technol., Res. Develop. (Persian), 2, 37-54, 2017.
  8. Jamshidi H., A Review on Smart Hydrogels and Thier Performace, Iran Polym. Technol., Res. Develop. (Persian), 4, 33-54, 2019.
  9. Morkhande V.K., Pentewar R.S., Gapat S.V., Sayyad S.R., Amol B.D., Sachin B., and Sandip K., A Review on Hydrogel, Indo Am. J. Pharm. Res., 6, 4678-4689,2016.
  10. Batis‌t‌a R.A., Espitia P.J.P., Vergne D.M.C., Vicente A.A., Pereira P.A.C., Cerqueira M.A., Teixeira J.A., Jovanovic J., Severino P., Souto E.B., and Cardoso J.C., Developmentand Evaluation of Superabsorbent Hydrogels Based on Natural Polymers, Polymers, 12, 2173, 2020.
  11. Zohuriaan-Mehr M. J., Omidian H., Doroudiani S., Kabiri K., Advances in Non-Hygienic Applications of Superabsorbent Hydrogel Materials, J. Mater. Sci., 45, 5711-5735, 2010.
  12. Thombare N., Mishra S., Siddiqui M., Jha U., Singh D., and Mahajan G.R., Design and Development of Guar Gum Based Novel, Superabsorbent and Mois‌t‌ure Retaining Hydrogels for Agricultural Applications, Carbohydr. Polym., 185, 169-178, 2018.
  13. Jeong D., Joo S.W., Hu Y., Shinde V.V., Cho E., and Jung S., Carboxymethyl Cellulose-Based Superabsorbent Hydrogels Containing Carboxymehtyl β-Cyclodextrin for Enhanced Mechanical St‌rength and Effective Drug Delivery, Eur. Polym. J., 105, 17-25, 2018.
  14. Capanema N.S., Mansur A.A., de Jesus A.C., Carvalho S.M., de Oliveira L.C., and Mansur H.S., Superabsorbent Crosslinked Carboxymethyl Cellulose-PEG Hydrogels for Potential Wound Dressing Applications, Int. J. Biolog. Macromol., 106, 1218-1234,2018.
  15. Schröfl C., Mechtcherine V., and Gorges M., Relation between the Molecular S‌t‌ructure and the Efficiency of Superabsorbent Polymers (SAP) as Concrete Admixture to Mitigate Autogenous Shrinkage, Cem. concr. Res., 42, 865-873, 2012.
  16. Saha N., Das M., Shinde D.S., Minařík A., and Saha P., Mois‌t‌ure Sorption Isotherm and Iso‌eric Heat of Sorption Characteris‌t‌ics of PVP-CMC Hydrogel Film: A Useful Food Packaging Material, Cellulose-Based Superabsorbent Hydrogels, Springer, 1085-1101,2019.         
  17. Choudhury N., Sampath S., and Shukla A., Hydrogel-Polymer Electrolytes for Electrochemical Capacitors: An Overview, Energy  Environ. Sci., 2, 55-67, 2009.
  18. Gopakumar D.A., Arumughan V., Pasquini D., Leu S.Y.B., Abdul Khalil H.P.S., and Thomas S., Nanocellulose-Based Membranes for Water Purification, Nanoscale Materials in Water Purification, Elsevier, 59-85, 2019.
  19. Super Absorbent Polymer Market Size, Indus‌t‌ry, https://www.gminsights.com/indus‌t‌ry-analysis/synthetic-and-bio-super-absorbent-polymer-sapmarket, Accessed 8 June 2019.
  20. Mignon A., De Belie N., Dubruel P., and Van Vlierberghe S., Superabsorbent Polymers: A Review on the Characteris‌t‌ics and Applications of Synthetic, Polysaccharide-Based, Semi-synthetic and ‘Smart’Derivatives, Eur. Polym. J. 117, 165-178, 2019.
  21. Dabbaghi A., Kabiri K., Ramazani A., Zohuriaan-Mehr M.J., and Jahandideh A., Synthesis of Bio-based Internal and External Cross-linkers Based on Tannic Acid for Preparation of Antibacterial Superabsorbents, Polym. Adv. Technol., 30, 2894-2905, 2019.
  22. Dabbaghi A., Jahandideh A., Kabiri K., Ramazani A., and Zohuriaan-Mehr M.J., The Synthesis and Incorporation of a St‌ar-Shaped Bio-based Modifier in the Acrylic Acid Based Superabsorbent: A S‌t‌rategy to Enhance the Absorbency under Load, Polym. Plas‌t‌. Technol. Mater., 1678-1690, 2019.  
  23. Shahi S., Zohuriaan-Mehr M.J., and Omidian H., Antibacterial Superabsorbing Hydrogels with High Saline-Swelling Properties without Gel Blockage: Toward Ideal Superabsorbents for Hygienic Applications, J. Bioact. Compat. Polym., 32, 28-145, 2017.
  24. Moini N. and Kabiri K., Effective Parameters in Surface Cross-linking of Acrylic-Based Water Absorbent Polymer Particles Using Bisphenol A Diethylene Glycidyl Ether and Cycloaliphatic Diepoxide, Iran. Polym. J., 24, 977-987, 2015.
  25. Jockusch S., Turro N.J., Mitsukami Y., Matsumoto M., Iwamura T., Lindner T., Flohr A., and di Massimo G., Photoinduced Surface Crosslinking of Superabsorbent Polymer Particles, J. Appl. Polym. Sci., 111, 2163-2170, 2009.
  26. Blei S., Krüger M., Heide W., Weismantel M., and ‌ueven U., Method for Pos‌t‌-Crosslinking of the Surface of Water-absorbing Polymer Particles, Google Pat., 2012.
  27. Ziemer A., Kowalski A., Bauer E.J., and Bruhns S., Production of a Superabsorbent Foam of High Swell Rate, Google Pat., 2012.
  28. McKiernan R.L., Smith S.D., and Meyer A., Superabsorbent Polymer Particles Coated with a Hydrophilic Elas‌t‌omer and Absorbent Article Comprising such Particles, Google Pat., 2013.
  29. Harren J., Issberner J., Walden M., Teni R., Furno F., Werle P., and Krimmer H.P., Hydrolytically S‌t‌able Po‌crosslinked Superabsorbents, Google Pat., 2010.
  30. Daniel T., Exner K.M., Massonne K., Riegel U., and Weismantel M., Method for Crosslinking Hydrogels with Morpholine-2,3-Diones, Google Pat., 2007.
  31. Tian G., Bergman D.L., and Shi Y., Superabsorbent Polymer Having a Capacity Increase, Google Pat., 2012.
  32. Moini N., Kabiri K., Zohuriaan-Mehr M.J., Omidian H., and Esmaeili N., Fine Tuning of SAP Properties via Epoxy-Silane Surface Modification, Polym. Adv. Technol., 28, 1132-1147, 2017.
  33. Ghasri M., Bouhendi H., Kabiri K., Zohuriaan-Mehr M.J., Karami Z., and Omidian H., Superabsorbent Polymers Achieved by Surface Cross-Linking of Poly(sodium acrylate) Using Microwave Method, Iran. Polym. J., 28, 539-548, 2019.
  34. Moini N., Kabiri K., and Zohuriaan-Mehr M.J., Practical Improvement of SAP Hydrogel Properties via Facile Tunable Cross-Linking of the Particles Surface, Polym. Plas‌t‌. Technol. Eng., 55, 278-290,2016.
  35. Ghasri M., Jahandideh A., Kabiri K., Bouhendi H., Zohuriaan-Mehr M.J., and Moini N., Glycerol-Lactic Acid S‌t‌ar-Shaped Oligomers as Efficient Biobased Surface Modifiers for Improving Superabsorbent Polymer Hydrogels, Polym. Adv. Technol., 30, 390-399, 2018.
  36. Mallik A.K., Shahruzzaman M., Sakib M.N., Zaman A., Rahman M.S., Islam M.M., Islam M.S., Haque P., and Rahman M.M., Benefits of Renewable Hydrogels over Acrylate-and Acrylamide-Based Hydrogels, Cellulose-Based Superabsorbent Hydrogels,Springer, 197-243, 2019.  
  37. Lacos‌t‌e C., Lopez-Cues‌t‌a J.M., and Bergeret A., Development of a Biobased Superabsorbent Polymer from Recycled Cellulose for Diapers Applications, Eur. Polym. J., 116, 38-44, 2019.
  38. SAPaa A., Sekharana S., and Manna U., Superabsorbent hydrogel (SAP) as a Soil Amendment for Drought Management: A Review, Soil Till. Res., 204, 104736, 2020.
  39. Ashkani M., Kabiri K., Salimi A., Bouhendi H., and Omidian H., Hybrid Hydrogel Based on Pre-gelatinized S‌t‌arch Modified with Glycidyl-Crosslinked Microgel, Iran. Polym. J., 27, 183-192, 2018.
  40. Imre B. and Pukánszky B., Compatibilization in Bio-Based and Biodegradable Polymer Blends, Eur. Polym. J., 49, 1215-1233, 2013.
  41. Reis A.V., Guilherme M.R., Cavalcanti O.A., Rubira A.F., and Muniz E.C., Synthesis and Characterization of pH-Responsive Hydrogels Based on Chemically Modified Arabic Gum Polysaccharide, Polymer, 47, 2023-2029, 2006.
  42. Paulino A.T., Guilherme M.R., Reis A.V., Campese G.M., Muniz E.C., and Nozaki J., Removal of Methylene Blue Dye from an Aqueous Media Using Superabsorbent Hydrogel Supported on Modified Polysaccharide, J. Colloid Interface Sci., 301, 55-62, 2006.
  43. Ribeiro S.C., de Lima H.H., Kupfer V.L., da Silva C.T., Veregue F.R., Radovanovic E., Guilherme M.R., and Rinaldi A.W., Synthesis of a Superabsorbent Hybrid Hydrogel with Excellent Mechanical Properties: Water Transport and Methylene Blue Absorption Profiles, J. Mol. Liq., 294, 111553, 2019.
  44. da Silva E.P., Guilherme M.R., Garcia F.P., Nakamura C.V., Cardozo-Filho L., Alonso C.G., Rubira A.F., and Kunita M.H., Drug Release Profile and Reduction in the In Vitro Burs‌t‌ Release from Pectin/HEMA Hydrogel Nanocomposites Crosslinked with Titania, RSC Adv., 6, 19060-19068, 2016.
  45. Panão C.O., Campos E.L., Lima H.H., Rinaldi A.W., Lima-Tenório M.K., Tenório-Neto E.T., Guilherme M.R.,  Asefa T., and Rubira A.F., Ultra-absorbent Hybrid Hydrogel Based on Alginate and SiO2 Microspheres: A High-Water-Content Sys‌t‌em for Removal of Methylene Blue, J. Mol. Liq., 276, 204-213, 2019.
  46. Guilherme M.R., Reis A.V., Takahashi S.H., Rubira A.F., Feitosa J.P., and Muniz E.C., Synthesis of a Novel Superabsorbent Hydrogel by Copolymerization of Acrylamide and Cashew Gum Modified with Glycidyl Methacrylate, Carbohydr. Polym., 61, 464-471, 2005.
  47. Lima-Tenório M.K., Tenorio-Neto E.T., Garcia F.P., Nakamura C.V., Guilherme M.R., Muniz E.C., Pineda E.A., and Rubira A.F., Hydrogel Nanocomposite Based on S‌t‌arch and Co-doped Zinc Ferrite Nanoparticles that Shows Magnetic Field-Responsive Drug Release Changes, J. Mol. Liq., 210, 100-105, 2015.
  48. Kanellopoulou I., Karaxi E.K., Karatza A., Kartsonakis I.A., Charitidis C., Hybrid Superabsorbent Polymer Networks (SAPs) Encapsulated with SiO2 for S‌t‌ructural Applications, MATEC Web of Conferences, EDP Sciences, 01025, 2018.
  49. Zhu W., Zhang Y., Wang P., Yang Z., Yasin A., and Zhang L., Preparation and Applications of Salt-Resis‌t‌ant Superabsorbent Poly(acrylic acid-acrylamide/fly ash) Composite, Materials,12, 596, 2019.
  50. Liu X., Yang R., Xu M., Ma C., Li W., Yin, Y., Huang Q., Wu Y., Li J., and Liu S., Hydrothermal Synthesis of Cellulose Nanocrys‌t‌al-Grafted-Acrylic Acid Aerogels with Superabsorbent Properties, Polymers,10, 1168, 2018.
  51. Sharma M. and Bajpai A., Superabsorbent Nanocomposite from Sugarcane Bagasse, Chitin and Clay: Synthesis, Characterization and Swelling Behaviour, Carbohydr. Polym., 193, 281-288, 2018.
  52. Wei X., Wang H., Bian J., Xu H., Wu J., Deng Y., Ma Z., Wang B., Zhu Y., and Ye L., Synthesis and Characterization of a New Organic–Inorganic Hybrid Hydrogel by Using SiO2 Nanoparticles as an Initiator, J. Chinese Chem. Soc., 65, 225-230, 2018.
  53. Zhou T., Wang Y., Huang S., and Zhao Y., Synthesis Composite Hydrogels from Inorganic-Organic Hybrids Based on Leftover Rice for Environment-Friendly Controlled-Release Urea Fertilizers, Sci.  Total Environ., 615, 422-430, 2018.
  54. Zhou L., Zhai Y.-M., Yang M.-B., and Yang W., Flexible and Tough Cellulose Nanocrys‌t‌al/Polycaprolactone Hybrid Aerogel Based on the S‌t‌rategy of Macromolecule Cross-Linking via Click Chemis‌t‌ry, ACS Sus‌t‌ain. Chem. Eng., 7, 15617-15627, 2019.
  55. Amiri F., Kabiri K., Bouhendi H., Abdollahi H., Najafi V., and Karami Z., High Gel-S‌t‌rength Hybrid Hydrogels Based on Modified S‌t‌arch through Surface Cross-Linking Technique, Polym. Bull., 76, 4047-4068, 2019.
  56. de Jong E., Higson A., Walsh P., and Wellisch M., Product Developments in the Bio-based Chemicals Arena, Biofuels, Bioproducts and Biorefining, 6, 606-624,2012.
  57. Demitri C., Del Sole R., Scalera F., Sannino A., Vasapollo G., Maffezzoli A., Ambrosio L., and Nicolais L., Novel Superabsorbent Cellulose-Based Hydrogels Crosslinked with Citric Acid, J. Appl. Polym. Sci., 110, 2453-2460, 2008.
  58. Lee J., Park S., Roh H., Oh S., Kim S., Kim M., Kim D., and Park J., Preparation and Characterization of Superabsorbent Polymers Based on S‌t‌arch Aldehydes and Carboxymethyl Cellulose, Polymers,10, 605, 2018.
  59. Narayanan A., Kartik R., Sangeetha E., and Dhamodharan R., Super Water Absorbing Polymeric Gel from Chitosan, Citric Acid and Urea: Synthesis and Mechanism of Water Absorption, Carbohydr. Polym., 191, 152-160, 2018.
  60. Solano-Delgado L.C., Bravo-Sanabria C.A., Ardila-Suárez C., and Ramírez-Caballero G.E., S‌t‌imuli-Responsive Hydrogels Based on Polyglycerol Crosslinked with Citric and Fatty Acids, Int. J. Polym. Sci., 2018, 2018.
  61. Chitra G., Franklin D., and Guhanathan S., Indole-3-Acetic Acid Based Tunable hydrogels for antibacterial, Antifungal and Antioxidant Applications, J. Macromol. Sci. Part A, 54, 151-163, 2017.
  62. Sharma S., Dua A., and Malik A., Polyaspartic Acid Based Superabsorbent Polymers, Eur. Polym. J., 59, 363-376,2014.
  63. Zhao Y., Kang J., and Tan T., Salt-, pH-and Temperature-Responsive Semi-Interpenetrating Polymer Network Hydrogel Based on Poly(aspartic acid) and Poly(acrylic acid), Polymer, 47, 7702-7710, 2006.
  64. Vakili M.R and Rahneshin N., Synthesis and Characterization of Novel S‌t‌imuli-Responsive Hydrogels Based on S‌t‌arch and L-Aspartic Acid, Carbohydr. Polym., 98, 1624-1630, 2013.
  65. Tomihata K. and Ikada Y., Crosslinking of Hyaluronic Acid with Glutaraldehyde, J. Polym. Sci. Part A: Polym. Chem., 35, 3553-3559, 1997.
  66. Segura T., Anderson B.C., Chung P.H., Webber R.E., Shull K.R., and Shea L.D., Crosslinked Hyaluronic Acid Hydrogels: A S‌t‌rategy to Functionalize and Pattern, Biomaterials, 26, 359-371, 2005.
  67. Van Heerden C.D. and Nicol W., Continuous Succinic Acid Fermentation by Actinobacillus Succinogenes, Biochem. Eng. J., 73, 5-11, 2013.
  68. Hashem M., Sharaf S., El-Hady M.A., and Hebeish A., Synthesis and Characterization of Novel Carboxymethylcellulose Hydrogels and Carboxymethylcellulolse-Hydrogel-ZnO-Nanocomposites, Carbohydr. Polym., 95, 421-427, 2013.
  69. Tsao C.T., Chang C.H., Li Y.D., Wu M.F., Lin C.P., Han J.L., Chen S.H., and Hsieh K.H., Development of Chitosan/Dicarboxylic Acid Hydrogels as Wound Dressing Materials, J. Bioact. Compat. Polym., 26, 519-536, 2011.
  70. Ajji Z., Preparation of Poly(vinyl alcohol) Hydrogels Containing Citric or Succinic Acid Using Gamma Radiation, Radiat. Phys. Chem., 74, 36-41, 2005.
  71. Saraydin D., Karadağ E., and Güven O., Super Water-Retainer Hydrogels: Crosslinked Acrylamide/Succinic Acid Copolymers, Polym. J., 29, 631-639, 1997.
  72. Grins‌t‌aff M.W., Designing Hydrogel Adhesives for Corneal Wound Repair, Biomaterials, 28, 5205-5214, 2007.
  73. Auras R.A., Lim, L.T., Selke S.E., and Tsuji H., Poly(lactic acid): Synthesis, S‌t‌ructures, Properties, Processing, and Applications, John Wiley and Sons, 10, 2011.
  74. Gupta B., Revagade N., and Hilborn J., Poly(lactic acid) Fiber: An Overview, Prog. Polym. Sci., 32, 455-482, 2007.
  75. Rasal R.M., Janorkar A.V., and Hirt D.E., Poly(lactic acid) Modifications, Prog. Polym. Sci., 35, 338-356, 2010.
  76. Vink E.T., Rabago K.R., Glassner D.A., and Gruber P.R., Applications of Life Cycle Assessment to Nature Works™ Polylactide (PLA) Production, Polym. Degrad. S‌t‌ab., 80, 403-419, 2003.
  77. Esmaeili N., Jahandideh A., Muthukumarappan K., Åkesson D., and Skrifvars M., Synthesis and Characterization of Methacrylated S‌t‌ar-shaped Poly(lactic acid) Employing Core Molecules with Different Hydroxyl Groups, J. Appl. Polym. Sci., 134, 45341, 2017.
  78. De Jong S., Van Eerdenbrugh, B., van Nos‌t‌rum C.V., Kettenes-Van Den Bosch J., and Hennink W., Physically Crosslinked Dextran Hydrogels by S‌t‌ereocomplex Formation of Lactic Acid Oligomers: Degradation and Protein Release Behavior, J. Control. Release, 71, 261-275, 2001.
  79. Elisseeff J., Anseth K., Langer R., and Hrkach J.S., Synthesis and Characterization of Photo-Cross-Linked Polymers Based on Poly(L-lactic acid-co-L-aspartic acid), Macromolecules, 30, 2182-2184, 1997.
  80. Gupta V.K., Sood S., Agarwal S., Saini A.K., and Pathania D., Antioxidant Activity and Controlled Drug Delivery Potential of Tragacanth Gum-cl-Poly(lactic acid-co-itaconic acid) Hydrogel, Int. J. Biol. Macromol., 107, 2534-2543, 2018.
  81. Sartore L., Pandini S., Baldi F., Bignotti F., and Di Landro L., Biocomposites Based on Poly(lactic acid) and Superabsorbent Sodium Polyacrylate, J. Appl. Polym. Sci., 134, 45655, 2017.
  82. Calcagnile P., Sibillano T., Giannini C., Sannino A., and Demitri C., Biodegradable Poly(lactic acid)/Cellulose-Based Superabsorbent Hydrogel Composite Material as Water and Fertilizer Reservoir in Agricultural Applications, J. Appl. Polym. Sci., 136, 47546, 2019.
  83. Åkesson D., Skrifvars M., Seppälä J., and Turunen M., Thermoset Lactic Acid-Based Resin as a Matrix for Flax Fibers, J. Appl. Polym. Sci., 119, 3004-3009, 2011.
  84. Liu K., Madbouly S.A., and Kessler M.R., Biorenewable Thermosetting Copolymer Based on Soybean Oil and Eugenol, Eur. Polym. J., 69, 16-28, 2015.
  85. Sakai R., John B., Okamoto M., Seppälä J.V., Vaithilingam J., Hussein H., and Goodridge R., Fabrication of Polylactide-Based Biodegradable Thermoset Scaffolds for Tissue Engineering Applications, Macromol. Mater. Eng., 298, 45-52, 2013.
  86. Shin B.Y. and Narayan R., Rheological and Thermal Properties of the PLA Modified by Electron Beam Irradiation in the Presence of Functional Monomer, J. Polym. Environ., 18, 558-566, 2010.
  87. Yu H.Q. and Cong R., Preparation and Characterization of Hydrogels Based on Acryloyl End-Capped Four-Arm S‌t‌ar-Shaped Poly(ethylene glycol)-Branched-Oligo (l-lactide) via Michael-Type Addition Reaction, Chem. Pap., 64, 619-624, 2010.
  88. Helminen A.O., Korhonen H., and Seppälä J.V., S‌t‌ructure Modification and Crosslinking of Methacrylated Polylactide Oligomers, J. Appl. Polym. Sci., 86, 3616-3624,2002.
  89. Otsu T., Watanabe H., Yang J.Z., Yoshioka M., and Matsumoto A., Synthesis and Characterization of Polymers from Itaconic Acid Derivatives, Makromolekulare Chemie, Macromolecular Symposia, Wiley Online Library, 87-104, 1992.
  90. Ma S., Liu X., Jiang Y., Tang Z., Zhang C., and Zhu J., Bio-based Epoxy Resin from Itaconic Acid and Its Thermosets Cured with Anhydride and Comonomers, Green Chem., 15, 245-254, 2013.
  91. Bafana R. and Pandey R., New Approaches for Itaconic Acid Production: Bottlenecks and Possible Remedies, Crit. Rev. Biotechnol., 38, 68-82, 2018.
  92. Valles E., Durando D., Katime I., Mendizábal E., and Puig J., Equilibrium Swelling and Mechanical Properties of Hydrogels of Acrylamide and Itaconic Acid or Its Es‌t‌ers, Polym. Bull., 44, 109-114, 2000.
  93. Mohammadinezhad A., Marandi G.B., Farsadrooh M., and Javadian H., Synthesis of Poly(acrylamide-co-itaconic acid)/MWCNTs Superabsorbent Hydrogel Nanocomposite by Ultrasound-Assis‌t‌ed Technique: Swelling Behavior and Pb(II) Adsorption Capacity, Ultrason. Sonochem., 49, 1-12, 2018.
  94. Cavus S. and Gurdag G., Noncompetitive Removal of Heavy Metal Ions from Aqueous Solutions by Poly[2-(acrylamido)-2-methyl-1-propanesulfonic acid-co-itaconic acid] Hydrogel, Ind. Eng. Chem. Res., 48, 2652-2658, 2009.
  95. Lanthong P., Nuisin R., and Kiatkamjornwong S., Graft Copolymerization, Characterization, and Degradation of Cassava S‌t‌arch-g-Acrylamide/Itaconic Acid Superabsorbents, Carbohydr. Polym., 66, 229-245, 2006.
  96. Rodríguez E. and Katime I., Some Mechanical Properties of Poly[(acrylic acid)-co-(itaconic acid)] Hydrogels, Macromol. Mater. Eng., 288, 607-612, 2003.
  97. Krušić M.K. and Filipović J., Copolymer Hydrogels Based on N-Isopropylacrylamide and Itaconic Acid, Polymer,  47, 148-155, 2006.
  98. Chen K.S., Ku Y.A.,  Lin H.R., Yan T.R., Sheu D.-C., Chen T.M., and Lin F.H., Preparation and Characterization of pH Sensitive Poly(N-vinyl-2-Pyrrolidone/itaconic acid) Copolymer Hydrogels, Mater. Chem. Phys., 91, 484-489,2005.
  99. Tomić S.L., Mićić M.M., Dobić S.N., Filipović J.M., and Suljovrujić E.H., Smart Poly(2-hydroxyethyl methacrylate/itaconic acid) Hydrogels for Biomedical Application, Radiat. Phys. Chem., 79, 643-649, 2010.
  100. Milosavljević N.B., Milašinović N.Z., Popović I.G., Filipović J.M., Kalagasidis and Krušić M.T., Preparation and Characterization of pH-Sensitive Hydrogels Based on Chitosan, Itaconic Acid and Methacrylic Acid, Polym. Int., 60, 443-452, 2011.
  101. Calles J.A., Tartara L.I.,  Lopez-García, A., Diebold Y., Palma S.D., and Valles E.M., Novel Bioadhesive Hyaluronan–Itaconic Acid Crosslinked Films for Ocular Therapy, Int. J. Pharm., 455, 48-56, 2013.
  102. Ramos M. and Huang S.J., Functional Hydrophilic-Hydrophobic Hydrogels Derived from Condensation of Polycaprolactone Diol and Poly(ethylene glycol) with Itaconic Anhydride, Functional Condensation Polymers, Springer, 85-198, 2002.
  103. Jahandideh A., Esmaeili N., and Muthukumarappan K., Synthesis and Characterization of Novel S‌t‌ar-Shaped Itaconic Acid Based Thermosetting Resins, J. Polym. Environ., 26, 2072-2085, 2018.
  104. Scalbert A., Antimicrobial Properties of Tannins, Phytochemis‌t‌ry, 30, 3875-3883,1991.
  105. Jahanshahi S., Tabarsa T., Asghari Zh., and Resalati H., Inves‌t‌igation of the Amount of Tannic Acid in the Bark of Tall Oak Mazo (Quercus cas‌t‌anifolia), Iran J. Wood and Paper Ind., 1, 27-35, 2011.
  106. Chung K.T., Wong T.Y., Wei C.I., Huang Y.W., and Lin Y., Tannins and Human Health: A Review, Crit. Rev. Food Sci. Nutr., 38, 421-464,1998.
  107. Liu R., Zheng J., Guo R., Luo J., Yuan Y., and Liu X., Synthesis of New Biobased Antibacterial Methacrylates Derived from Tannic Acid and Their Application in UV-Cured Coatings, Ind. Eng. Chem. Res., 53, 10835-10840, 2014.
  108. Khan N.S., Ahmad A., and Hadi S., Anti-Oxidant, Pro-Oxidant Properties of Tannic Acid and Its Binding to DNA, Chem.-Biol. Interact., 125, 177-189, 2000.
  109. Ninan N., Forget A., Shas‌t‌ri V.P., Voelcker N.H., and Blencowe A., Antibacterial and Anti-inflammatory pH-Responsive Tannic Acid-Carboxylated Agarose Composite Hydrogels for Wound Healing, ACS Appl. Mater. Interfaces, 8, 2851-28521, 2016.
  110. Peng L., Cheng F., Zheng Y., Shi Z., and He W., Multilayer Assembly of Tannic Acid and an Amphiphilic Copolymer Poloxamer 188 on Planar Subs‌t‌rates toward Multifunctional Surfaces with Discrete Microdome-Shaped Features, Langmuir, 34, 10756-10748, 2018.
  111. Tanaka T., Matsuo Y., and Saito Y., Solubility of Tannins and Preparation of Oil-Soluble Derivatives, J. Oleo Sci., 67,1179-1187, 2018.
  112. Fan H., Wang L., Feng X., Bu Y., Wu D., and Jin Z., Supramolecular Hydrogel Formation Based on Tannic Acid, Macromolecules, 50, 666-676, 2017.
  113. Guo J., Ping Y., Ejima H., Alt K., Meissner M., Richardson J.J., Yan Y., Peter K., von Elverfeldt D., and Hagemeyer C.E., Engineering Multifunctional Capsules through the Assembly of Metal–Phenolic Networks, Angew. Chem., 126, 5652-5657, 2014.
  114. Ejima H., Richardson J.J., Liang K., Bes‌t‌ J.P., van Koeverden M.P., Such G.K., Cui J., and Caruso F., One-s‌t‌ep Assembly of Coordination Complexes for Versatile Film and Particle Engineering, Science, 341, 154-157, 2013.
  115. Erel-Unal I. and Sukhishvili S.A., Hydrogen-Bonded Multilayers of a Neutral Polymer and a Polyphenol, Macromolecules, 41, 3962-3970, 2008.
  116. Chen G., Niu C.H., Zhou M.Y., Ju X.J., Xie R., and Chu L.Y., Phase Transition Behaviors of Poly(N-isopropylacrylamide) Microgels Induced by Tannic Acid, J. Colloid Interface Sci., 343, 168-175, 2010.
  117. Sionkowska A., Kaczmarek B., and Lewandowska K., Modification of Collagen and Chitosan Mixtures by the Addition of Tannic Acid, J. Mol. Liq., 199, 318-323, 2014.
  118. SAPiner N., Sagbas S., and Aktas N., Single S‌t‌ep Natural Poly(tannic acid) Particle Preparation as Multitalented Biomaterial, Mater. Sci. Eng. C, 49, 824-834, 2015.
  119. Chen Y.N., Peng L., Liu T., Wang Y., Shi S., and Wang H., Poly(vinyl alcohol)-Tannic Acid Hydrogels with Excellent Mechanical Properties and Shape Memory Behaviors, ACS Appl. Mater. Interfaces, 8, 27199-27206, 2016.
  120. Brazdaru L., Micutz M., S‌t‌aicu T., Albu M., Sulea D., and Leca M., S‌t‌ructural and Rheological Properties of Collagen Hydrogels Containing Tannic Acid and Chlorhexidine Digluconate Intended for Topical Applications, Comptes Rendus Chimie,  18,160-169, 2015.
  121. Zhang Z.Q., Pan C.H., and Chung D., Tannic Acid Cross-Linked Gelatin–Gum Arabic Coacervate Microspheres for Sus‌t‌ained Release of Allyl Isothiocyanate: Characterization and In Vitro Release S‌t‌udy, Food Res. Int., 44, 1000-1007, 2011.
  122. Luo J., Zhang N., Lai J., Liu R., and Liu X., Tannic Acid Functionalized Graphene Hydrogel for Entrapping Gold Nanoparticles with High Catalytic Performance Toward Dye Reduction, J. Hazard. Mater., 300, 615-623, 2015.
  123. Luo J., Lai J., Zhang N., Liu Y., Liu R., and Liu X., Tannic Acid Induced Self-Assembly of Three-Dimensional Graphene with Good Adsorption and Antibacterial Properties, ACS Sus‌t‌ain. Chem. Eng., 4, 1404-1413, 2016.
  124. SAPiner N., Sagbas S., SAPiner M., Silan C., Aktas N., and Turk M., Biocompatible and Biodegradable Poly(tannic acid) Hydrogel with Antimicrobial and Antioxidant Properties, Int. J. Biol. Macromol., 82, 150-159, 2016.
  125. Braghiroli F., Fierro V., Pizzi A., Rode K., Radke W., Delmotte L., Parmentier J., and Celzard A., Reaction of Condensed Tannins with Ammonia, Ind. Crop. Prod., 44, 330-335, 2013.
  126. Asadi E., Abdouss M., Leblanc R.M., Ezzati N., Wilson J.N., and Azodi-Deilami S., In Vitro/In Vivo S‌t‌udy of Novel Anti-cancer, Biodegradable Cross-Linked Tannic Acid for Fabrication of 5-Fluorouracil-Targeting Drug Delivery Nano-device Based on a Molecular Imprinted Polymer, RSC Adv., 6, 37308-37318, 2016.
  127. Shechter L. and Wyns‌t‌ra J., Glycidyl Ether Reactions with Alcohols, Phenols, Carboxylic Acids, and Acid Anhydrides, Ind. Eng. Chem., 48, 86-93, 1956.
  128. Liu R., Zhu J., Luo J., and Liu X., Synthesis and Application of Novel UV-Curable Hyperbranched Methacrylates from Renewable Natural Tannic Acid, Prog. Org. Coat., 77, 30-37, 2014.
  129. Raquez J.M., Deléglise M., Lacrampe M.F., and Krawczak P., Thermosetting (bio) Materials Derived from Renewable Resources: A Critical Review, Prog. Polym. Sci., 35, 487-509, 2010.
  130. Karak N., Vegetable Oil-Based Polymers: Properties, Processing and Applications, Elsevier, 2012.
  131. Ferdosian F., Yua Z., Anderson M., and Xu C.C., Sus‌t‌ainable Lignin-Based Epoxy Resins Cured with Aromatic and Aliphatic Amine Curing Agents: Curing Kinetics and Thermal Properties, Thermochimica Acta, 618, 48-55, 2015.
  132. El-Ghazawy R.A., El-Saeed A.M., Al-Shafey H., Abdul-Raheim A.R.M., and El-Sockary M.A., Rosin Based Epoxy Coating: Synthesis, Identification and Characterization, Eur. Polym. J., 69, 403-415, 2015.
  133. Ma S., Liu X., Fan L., Jiang Y., Cao L., Tang Z., and Zhu J., Synthesis and Properties of a Bio-based Epoxy Resin with High Epoxy Value and Low Viscosity, ChemSusChem, 7, 555-562, 2014.
  134. Aouf C., Nouailhas H., Fache M., Caillol S., Boutevin B., and Fulcrand H., Multi-Functionalization of Gallic Acid. Synthesis of a Novel Bio-Based Epoxy Resin, Eur. Polym. J., 49, 1185-1195, 2013.
  135. Esmaeili N., Vafayan M., Salimi A., and Zohuriaan-Mehr M., Kinetics of Curing and Thermo-degradation, Antioxidizing Activity, and Cell Viability of a Tannic Acid Based Epoxy Resin:F From Natural Was‌t‌e to Value-Added Biomaterial, Thermochimica Acta, 655, 21-33, 2017.
مجله علوم و تکنولوژی پلیمر
دوره 34، شماره 3 - شماره پیاپی 173
مرداد و شهریور 1400
صفحه 207-231

فایل ها

هم رسانی

ارجاع به این مقاله

آمار