Azo-linked nanoporous organic polymer for efficient capture of cationic dyes and radioactive iodine
Bibliographic record
Abstract
No abstract is available for this record. The assistant can identify its topic from the title, but cannot infer the study’s results.
Source: Not provided · Quality: missing
Research context
OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Carbon Dioxide Capture Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (99)
Show source-provided references
1. Kubra KT, Salman MS, Hasan MN (2021) Enhanced toxic dye removal from wastewater using biodegradable polymeric natural adsorbent. J Mol Liq 328:115468. https://doi.org/10.1016/j.molliq.2021.11546810.1016/j.molliq.2021.115468 ↗
2. Hynes NRJ, Kumar JS, Kamyab H et al (2020) Modern enabling techniques and adsorbents based dye removal with sustainability concerns in textile industrial sector -A comprehensive review. J Clean Prod 272:122636. https://doi.org/10.1016/j.jclepro.2020.12263610.1016/j.jclepro.2020.122636 ↗
3. Ganguly P, Sarkhel R, Das P (2020) Synthesis of pyrolyzed biochar and its application for dye removal: batch, kinetic and isotherm with linear and non-linear mathematical analysis. Surf Interface Anal 20:100616. https://doi.org/10.1016/j.surfin.2020.10061610.1016/j.surfin.2020.100616 ↗
4. Sarker M, Shin S, Jeong JH, Jhung SH (2019) Mesoporous metal-organic framework PCN-222(Fe): Promising adsorbent for removal of big anionic and cationic dyes from water. Chem Eng J 371:252. https://doi.org/10.1016/j.cej.2019.04.03910.1016/j.cej.2019.04.039 ↗
5. Van Duijn C (1962) Toxic and photodynamic effects of toluidine blue on living bull spermatoza. Exp Cell Res 26:373. https://doi.org/10.1016/0014-4827(62)90189-110.1016/0014-4827(62)90189-1 ↗
6. Fernández D, Abalde J, Torres E (2024) The biosorption capacity of the marine microalga phaeodactylum tricornutum for the removal of toluidine blue from seawater. Toxics 12(4):27710.3390/toxics12040277 ↗
7. Chi Z, Liu R, Sun Y, Wang M, Zhang P, Gao C (2010) Investigation on the toxic interaction of toluidine blue with calf thymus DNA. J Hazard Mater 175:274. https://doi.org/10.1016/j.jhazmat.2009.09.16010.1016/j.jhazmat.2009.09.160 ↗
8. Paul P, Suresh Kumar G (2013) Spectroscopic studies on the binding interaction of phenothiazinium dyes toluidine blue O, azure A and azure B to DNA. Spectrochim Acta A Mol Biomol Spectrosc 107:303. https://doi.org/10.1016/j.saa.2013.01.06310.1016/j.saa.2013.01.063 ↗
9. Kumar S, Kumari K, Singh SK, Dholakiya BZ, Jangir R (2023) Amorphous tetrazine–triazine-functionalized covalent organic framework for adsorption and removal of dyes. New J Chem 47:13676. https://doi.org/10.1039/D3NJ01913F10.1039/D3NJ01913F ↗
10. Xu T, An S, Peng C, Hu J, Liu H (2020) Construction of large-pore crystalline covalent organic framework as high-performance adsorbent for Rhodamine B dye removal. Ind Eng Chem Res 59:8315. https://doi.org/10.1021/acs.iecr.0c0030410.1021/acs.iecr.0c00304 ↗
11. Ghahari A, Farzad F, Azadnejad R (2024) The strategy of three-dimensional covalent organic frameworks to exclude dye contaminants in aqueous solutions. Npj Clean Water 7(1):27. https://doi.org/10.1038/s41545-024-00311-y10.1038/s41545-024-00311-y ↗
12. Howland MA, In Woolf AD (ed) (2022) History of Modern Clinical Toxicology, Academic Press
13. Sridharan G, Shankar AA (2012) Toluidine blue: a review of its chemistry and clinical utility. J Oral Maxillofac Pathol. https://doi.org/10.4103/0973-029X.9908110.4103/0973-029X.99081 ↗
14. Genwa KR, Chouhan A (2006) Role of heterocyclic dye (Azur A) as a photosensitizer in photogalvanic cell for solar energy conversion and storage: NaLS–ascorbic acid system. Sol Energy 80:1213. https://doi.org/10.1016/j.solener.2005.06.02010.1016/j.solener.2005.06.020 ↗
15. Daneshi S, Afshar EA, Taher MA, Karaman C, Karimi-Maleh H (2024) Fabrication of La2O3-SiO2 nanocomposite and investigation it’s photocatalytic performance for degradation of toluidine blue dye. Top Catal 67:628. https://doi.org/10.1007/s11244-024-01906-y10.1007/s11244-024-01906-y ↗
16. Uddin J, Idrees M, Ahmed H et al (2024) Biodegradation and decolorization of methylene blue, reactive Black-5, and toluidine blue-O from an aqueous solution using the polyphenol oxidase enzyme 7. Front Sustain Food Syst. https://doi.org/10.3389/fsufs.2023.132085510.3389/fsufs.2023.1320855 ↗
17. Roopan SM, Chellapandi T, Shebeer RM et al (2024) Advances and prospects in the development of GdVO4-based photocatalysts for water pollutants removal activity: a review. Nano Mater Sci 7(2):180–197. https://doi.org/10.1016/j.nanoms.2024.04.00110.1016/j.nanoms.2024.04.001 ↗
18. Maru K, Kalla S, Jangir R (2024) Efficient dye extraction from wastewater using Indium-MOF-immobilized polyvinylidene fluoride membranes with selective filtration for enhanced remediation. Langmuir 40:8144. https://doi.org/10.1021/acs.langmuir.4c0019410.1021/acs.langmuir.4c00194 ↗
19. Brues AM (1949) Biological hazards and toxicity of radioactive isotopes. J Clin Invest 28:128610.1172/JCI102196 ↗
20. Zaletel K, Mihovec A, Gaberscek S (2024) Characteristics of exposure to radioactive iodine during a nuclear incident. Radiol Oncol 58:45910.2478/raon-2024-0051 ↗
21. Yuan Y, Yu Q, Cao M et al (2021) Selective extraction of uranium from seawater with biofouling-resistant polymeric peptide. Nat Sustain 4:708. https://doi.org/10.1038/s41893-021-00709-310.1038/s41893-021-00709-3 ↗
22. MSA Naimi (2021) Reflection on Global and GCC Energy transition Pre and Post Covid 1910.46855/energy-proceedings-9481 ↗
23. R Lordan-Perret Restoring the Future of Nuclear Energy
24. Taylor R, Mathers G, Banford A (2023) The development of future options for aqueous recycling of spent nuclear fuels. Prog Nucl Energy 164:104837. https://doi.org/10.1016/j.pnucene.2023.10483710.1016/j.pnucene.2023.104837 ↗
25. Baker A, Fells A, Carrott MJ, Maher CJ, Hanson BC (2022) Process intensification of element extraction using centrifugal contactors in the nuclear fuel cycle. Chem Soc Rev 51:3964. https://doi.org/10.1039/D2CS00192F10.1039/D2CS00192F ↗
26. Abu-Khader MM (2009) Recent advances in nuclear power: a review. Prog Nucl Energy 51:225. https://doi.org/10.1016/j.pnucene.2008.05.00110.1016/j.pnucene.2008.05.001 ↗
27. Lu Z, Zhao W, Wu L et al (2021) Tunable electrochemical of electrosynthesized layer-by-layer multilayer films based on multi-walled carbon nanotubes and metal-organic framework as high-performance electrochemical sensor for simultaneous determination cadmium and lead. Sens Actuators B Chem 326:128957. https://doi.org/10.1016/j.snb.2020.12895710.1016/j.snb.2020.128957 ↗
28. Xie W, Cui D, Zhang SR, Xu YH, Jiang DL (2019) Iodine capture in porous organic polymers and metal–organic frameworks materials. Mater Horiz 6(8):1571–1595. https://doi.org/10.1039/C8MH01656A10.1039/C8MH01656A ↗
29. Mehra S, Singh M, Chadha P (2021) Adverse impact of textile dyes on the aquatic environment as well as on human beings. Toxicol Int 28:165. https://doi.org/10.18311/ti/2021/v28i2/2679810.18311/ti/2021/v28i2/26798 ↗
30. Bajoria A, Kanpariya J, Bera A (2024). In: Rahimpour MR, Makarem MA, Meshksar M (eds) Advances and technology development in greenhouse gases: emission, capture and conversion. Elsevier, UK
31. Wang D, Zhou Q, Yin Y et al (2024) Implications of Fukushima’s radioactive water discharge on global environmental sustainability. Environ Sci Technol 58:3061. https://doi.org/10.1021/acs.est.4c0095510.1021/acs.est.4c00955 ↗
32. Wang S, Vakili M, Guan T et al (2024) Adsorption of typical dyes in water by sponge based covalent organic frameworks: pore size and mechanism. Colloids Surf A Physicochem Eng Asp 685:133312. https://doi.org/10.1016/j.colsurfa.2024.13331210.1016/j.colsurfa.2024.133312 ↗
33. Patel HA, Je SH, Park J et al (2013) Unprecedented high-temperature CO2 selectivity in N2-phobic nanoporous covalent organic polymers. Nat Commun 4:1357. https://doi.org/10.1038/ncomms235910.1038/ncomms2359 ↗
34. Huo J, Luo B, Chen Y (2019) Crystalline covalent organic frameworks from triazine nodes as porous adsorbents for dye pollutants. ACS Omega 4:22504. https://doi.org/10.1021/acsomega.9b0317610.1021/acsomega.9b03176 ↗
35. Jiang J-X, Cooper AI (2010). In: Schröder M (ed) Functional metal-organic frameworks: gas storage separation and catalysis. Springer, Heidelberg
36. Akelah A, Sherrington DC (1981) Application of functionalized polymers in organic synthesis. Chem Rev 81:557. https://doi.org/10.1021/cr00046a00310.1021/cr00046a003 ↗
37. McKeown NB, Budd PM (2010) Exploitation of intrinsic microporosity in polymer-based materials. Macromolecules 43:5163. https://doi.org/10.1021/ma100639610.1021/ma1006396 ↗
38. Jiang J-X, Su F, Trewin A et al (2007) Conjugated microporous poly(aryleneethynylene) networks Angew. Chem Int Ed 46:8574. https://doi.org/10.1002/anie.20070159510.1002/anie.200701595 ↗
39. Mendoza-Cortés JL, Han SS, Furukawa H, Yaghi OM, Goddard WA III (2010) Adsorption mechanism and uptake of methane in covalent organic frameworks: theory and experiment. J Phys Chem A 114:10824. https://doi.org/10.1021/jp104413910.1021/jp1044139 ↗
40. Wood CD, Tan B, Trewin A et al (2007) Hydrogen storage in microporous hypercrosslinked organic polymer networks. Chem Mater 19:2034. https://doi.org/10.1021/cm070356a10.1021/cm070356a ↗
41. Ben T, Ren H, Ma S et al (2009) Targeted synthesis of a porous aromatic framework with high stability and exceptionally high surface area Angew. Chem Int Ed 48:9457. https://doi.org/10.1002/anie.20090463710.1002/anie.200904637 ↗
42. Katsoulidis AP, Kanatzidis MG (2011) Phloroglucinol based microporous polymeric organic frameworks with −OH functional groups and high CO2 capture capacity. Chem Mater 23:1818. https://doi.org/10.1021/cm103206x10.1021/cm103206x ↗
43. Schwab MG, Fassbender B, Spiess HW, Thomas A, Feng X, Müllen K (2009) Catalyst-free preparation of melamine-based microporous polymer networks through Schiff base chemistry. J Am Chem Soc 131:7216. https://doi.org/10.1021/ja902116f10.1021/ja902116f ↗
44. Mohanty P, Kull LD, Landskron K (2011) Porous covalent electron-rich organonitridic frameworks as highly selective sorbents for methane and carbon dioxide. Nat Commun 2:401. https://doi.org/10.1038/ncomms140510.1038/ncomms1405 ↗
45. Rose M, Böhlmann W, Sabo M, Kaskel S (2008) Element–organic frameworks with high permanent porosity. Chem Commun 21:2462–2464. https://doi.org/10.1039/B718925G10.1039/B718925G ↗
46. Rabbani MG, Reich TE, Kassab RM, Jackson KT, El-Kaderi HM (2012) High CO2 uptake and selectivity by triptycene-derived benzimidazole-linked polymers. Chem Commun 48:1141. https://doi.org/10.1039/C2CC16986J10.1039/C2CC16986J ↗
47. Esen C, Kumru B (2022) Photocatalyst-incorporated cross-linked porous polymer networks. Ind Eng Chem Res 61:10616. https://doi.org/10.1021/acs.iecr.2c0165810.1021/acs.iecr.2c01658 ↗
48. Patel HA, Karadas F, Canlier A et al (2012) High capacity carbon dioxide adsorption by inexpensive covalent organic polymers. J Mater Chem 22:8431. https://doi.org/10.1039/C2JM30761H10.1039/C2JM30761H ↗
49. Rong Y, He D, Malpass-Evans R et al (2017) High-utilisation nanoplatinum catalyst (Pt@ cPIM) obtained via vacuum carbonisation in a molecularly rigid polymer of intrinsic microporosity. Electrocatalysis 8(2):132–143. https://doi.org/10.1007/s12678-016-0347-510.1007/s12678-016-0347-5 ↗
50. Budd PM, Ghanem BS, Makhseed S, McKeown NB, Msayib KJ, Tattershall CE (2004) Polymers of intrinsic microporosity (PIMs): robust, solution-processable, organic nanoporous materials. Chem Commun 2:230–231. https://doi.org/10.1039/B311764B10.1039/B311764B ↗
51. Ren S, Dawson R, Laybourn A et al (2012) Functional conjugated microporous polymers: from 1,3,5-benzene to 1,3,5-triazine. Polym Chem 3:928. https://doi.org/10.1039/C2PY00585A10.1039/C2PY00585A ↗
52. Wang S, Xia X, Chen F-E (2022) Engineering of covalent organic framework-based advanced platforms for enzyme immobilization: strategies research progress, and prospects. Adv Mater Interfaces 9:2200874. https://doi.org/10.1002/admi.20220087410.1002/admi.202200874 ↗
53. Côté AP, Benin AI, Ockwig NW, O’Keeffe M, Matzger AJ, Yaghi OM (2005) Porous, crystalline, covalent organic frameworks. Science 310:1166. https://doi.org/10.1126/science.112041110.1126/science.1120411 ↗
54. Li Z, Yang Y-W (2022) Macrocycle-based porous organic polymers for separation, sensing, and catalysis. Adv Mater 34:2107401. https://doi.org/10.1002/adma.20210740110.1002/adma.202107401 ↗
55. Gao Z-Z, Wang Z-K, Wei L et al (2020) Water-soluble 3D covalent organic framework that displays an enhanced enrichment effect of photosensitizers and catalysts for the reduction of protons to H2. ACS Appl Mater Interfaces 12(1):1404–1411. https://doi.org/10.1021/acsami.9b1987010.1021/acsami.9b19870 ↗
56. Xiong Y-K, Du P, Huang S-J et al (2024) Polyhydroxy-azo porous organic polymers for efficient removal of organic pollutants from water. ACS Appl Polym Mater 6:5674. https://doi.org/10.1021/acsapm.4c0032910.1021/acsapm.4c00329 ↗
57. Cai Y, Li J, Zhang Q et al (2025) Ambient ultrafast green synthesis of cyclodextrin-based metal-organic framework through solvent-induced in-situ crystallization for high-efficiency capture of radioactive iodine. Sep Purif Technol 376:134078. https://doi.org/10.1016/j.seppur.2025.13407810.1016/j.seppur.2025.134078 ↗
58. Pan X, Qin X, Zhang Q, Ge Y, Ke H, Cheng G (2020) N- and S-rich covalent organic framework for highly efficient removal of indigo carmine and reversible iodine capture. Microporous Mesoporous Mater 296:109990. https://doi.org/10.1016/j.micromeso.2019.10999010.1016/j.micromeso.2019.109990 ↗
59. He D, Jiang L, Yuan K et al (2022) Synthesis and study of low-cost nitrogen-rich porous organic polyaminals for efficient adsorption of iodine and organic dye. Chem Eng J 446:137119. https://doi.org/10.1016/j.cej.2022.13711910.1016/j.cej.2022.137119 ↗
60. Yang D-A, Cho H-Y, Kim J, Yang S-T, Ahn W-S (2012) CO 2 capture and conversion using Mg-MOF-74 prepared by a sonochemical method. Energy Environ Sci 5(4):6465–6473. https://doi.org/10.1039/C1EE02234B10.1039/C1EE02234B ↗
61. Yadav A, Chong S, Riley BJ, McCloy JS, Goel A (2023) Iodine capture by Ag-loaded solid sorbents followed by Ag recycling and iodine immobilization: an end-to-end process. Ind Eng Chem Res 62:3635. https://doi.org/10.1021/acs.iecr.2c0435710.1021/acs.iecr.2c04357 ↗
62. Abdelnaby MM, Saleh TA, Zeama M, Abdalla MA, Ahmed HM, Habib MA (2022) Azo-linked porous organic polymers for selective carbon dioxide capture and metal ion removal. ACS Omega 7:14535. https://doi.org/10.1021/acsomega.1c0590510.1021/acsomega.1c05905 ↗
63. Dang Q-Q, Wang X-M, Zhan Y-F, Zhang X-M (2016) An azo-linked porous triptycene network as an absorbent for CO2 and iodine uptake. Polym Chem 7(3):643–647. https://doi.org/10.1039/C5PY01671A10.1039/C5PY01671A ↗
64. Zhou Z-B, Tian P-J, Yao J, Lu Y, Qi Q-Y, Zhao X (2022) Toward azo-linked covalent organic frameworks by developing linkage chemistry via linker exchange. Nat Commun 13:2180. https://doi.org/10.1038/s41467-022-29814-310.1038/s41467-022-29814-3 ↗
65. Chen J, Jiang C, Xing Z, Li J, Dai F, Peng Y (2023) Fluorine-functionalized 2D covalent organic frameworks with kgd topology for efficient C2H2/CO2 separation. New J Chem 47:6759. https://doi.org/10.1039/D3NJ00045A10.1039/D3NJ00045A ↗
66. Gupta SK, Kaleeswaran D, Nandi S, Vaidhyanathan R, Murugavel R (2017) Bulky isopropyl group loaded tetraaryl pyrene based azo-linked covalent organic polymer for nitroaromatics sensing and CO2 adsorption. ACS Omega 2(7):3572–3582. https://doi.org/10.1021/acsomega.7b0051510.1021/acsomega.7b00515 ↗
67. Maurin G, Serre C, Cooper A, Férey G (2017) The new age of MOFs and of their porous-related solids. Chem Soc Rev 46:3104. https://doi.org/10.1039/C7CS90049J10.1039/C7CS90049J ↗
68. Yaghi OM, O’Keeffe M, Ockwig NW, Chae HK, Eddaoudi M, Kim J (2003) Reticular synthesis and the design of new materials. Nature 423:705. https://doi.org/10.1038/nature0165010.1038/nature01650 ↗
69. Giri A, Khakre Y, Shreeraj G, Dutta TK, Kundu S, Patra A (2022) The order–disorder conundrum: a trade-off between crystalline and amorphous porous organic polymers for task-specific applications. J Mater Chem A 10:17077. https://doi.org/10.1039/D2TA01546C10.1039/D2TA01546C ↗
70. Brunauer S, Emmett PH, Teller E (1938) Adsorption of gases in multimolecular layers. J Am Chem Soc 60:309. https://doi.org/10.1021/ja01269a02310.1021/ja01269a023 ↗
71. Thommes M, Kaneko K, Neimark AV et al (2015) Physisorption of gases, with special reference to the evaluation of surface area and pore size distribution (IUPAC technical report). Pure Appl Chem 87:1051. https://doi.org/10.1515/pac-2014-111710.1515/pac-2014-1117 ↗
72. Sing K (1967) Adsorption, surface area, and porosity. Academic press, NY
73. Patel HA, Je SH, Park J, Jung Y, Coskun A, Yavuz CT (2014) Directing the structural features of N2-phobic nanoporous covalent organic polymers for CO2 capture and separation. Chem Eur J 20:772. https://doi.org/10.1002/chem.20130349310.1002/chem.201303493 ↗
74. Li S, Prasetya N, Ladewig BP (2019) Investigation of Azo-COP-2 as a photoresponsive low-energy CO2 adsorbent and porous filler in mixed matrix membranes for CO2/N2 separation. Ind Eng Chem Res 58:9959. https://doi.org/10.1021/acs.iecr.9b0076210.1021/acs.iecr.9b00762 ↗
75. Rauf MA, Qadri SM, Ashraf S, Al-Mansoori KM (2009) Adsorption studies of Toluidine Blue from aqueous solutions onto gypsum. Chem Eng J 150:90. https://doi.org/10.1016/j.cej.2008.12.00810.1016/j.cej.2008.12.008 ↗
76. Jangra A, Kumar R, Singh D et al (2024) Remediation of toluidine blue O dye from aqueous solution using surface functionalized magnetite nanoparticles. Water Pract Technol 19:1119. https://doi.org/10.2166/wpt.2024.06310.2166/wpt.2024.063 ↗
77. Tural B, Ertaş E, Enez B, Tural S (2024) Removal of lead (II) and toluidine blue from wastewater with new magnetic Bacillus niacini nano-biosorbent. Int J Environ Sci Technol 21:7431. https://doi.org/10.1007/s13762-024-05515-w10.1007/s13762-024-05515-w ↗
78. Sguillar M, Lakhmiri R, Eladnani I et al (2024) A novel biosorbent-based marine macroalgal biomass for efficient removal of toluidine blue and basic yellow 28 dyes-contaminated waters. Chem Phys Lett 843:141234. https://doi.org/10.1016/j.cplett.2024.14123410.1016/j.cplett.2024.141234 ↗
79. Brandao WQ, Maciel BG, de Araújo Lima EM, Mojica-Sanchez LC, da Silva RJ, de Melo CP (2023) Carboxymethylcellulose magnetic composite for adsorptive removal of cationic toluidine blue dye. Mater Chem Phys 303:127782. https://doi.org/10.1016/j.matchemphys.2023.12778210.1016/j.matchemphys.2023.127782 ↗
80. Li H, Huang H, Yan X, Liu C, Li L (2021) A calix[4]arene-crosslinked polymer for rapid adsorption of cationic dyes in water. Mater Chem Phys 263:124295. https://doi.org/10.1016/j.matchemphys.2021.12429510.1016/j.matchemphys.2021.124295 ↗
81. Reid C, Mulliken RS (1954) Molecular compounds and their spectra IV, the pyridine-iodine system1. J Am Chem Soc 76(15):3869–3874. https://doi.org/10.1021/ja01644a00110.1021/ja01644a001 ↗
82. Li B, Yin D, Chen L et al (2024) In-depth investigation of the iodine-nitrogen interaction mechanism using ab initio and density functional theory calculations. Comput Theor Chem 1241:114862. https://doi.org/10.1016/j.comptc.2024.11486210.1016/j.comptc.2024.114862 ↗
83. Li H, Zhang D, Cheng K, Li Z, Li P-Z (2023) Effective iodine adsorption by nitrogen-rich nanoporous covalent organic frameworks. ACS Appl Nano Mater 6:1295. https://doi.org/10.1021/acsanm.2c0494110.1021/acsanm.2c04941 ↗
84. Guo S-J, Zhang G-H, Zhu Q-H et al (2023) Efficient capture of iodine by charge-induced effect of nitrogen-rich ionic liquids. Chem Eng J 475:146221. https://doi.org/10.1016/j.cej.2023.14622110.1016/j.cej.2023.146221 ↗
85. Cheng K, Li H, Li Z, Li P-Z, Zhao Y (2023) Linking nitrogen-rich organic cages into isoreticular covalent organic frameworks for enhancing iodine adsorption capability. ACS Mater Lett 5:1546. https://doi.org/10.1021/acsmaterialslett.3c0021310.1021/acsmaterialslett.3c00213 ↗
86. Maru K, Kalla S, Jangir R (2025) Strategic design of novel zinc and cadmium metal-organic frameworks for enhanced, reversible, and multi-phase iodine sequestration. Small Methods. https://doi.org/10.1002/smtd.20250010110.1002/smtd.202500101 ↗
87. Chen S, Yuan L, Shi W (2025) Structure-activity relationship of covalent organic frameworks (COFs) for gaseous iodine adsorption. Natl Sci Open 4(1):20240026
88. Liu C, An X, Wang P et al (2025) Two step pore expansion assisted by KOH activation of nitrogen-doped biochar for enhanced gaseous iodine adsorption. Colloids Surf A Physicochem Eng Asp 709:136184. https://doi.org/10.1016/j.colsurfa.2025.13618410.1016/j.colsurfa.2025.136184 ↗
89. Yu J, Song L, Yang M et al (2025) Design, synthesis, and iodine adsorption performances of indole-derived porous organic polymers. Polymer 320:128106. https://doi.org/10.1016/j.polymer.2025.12810610.1016/j.polymer.2025.128106 ↗
90. Peng Y, Meng T, Lei H et al (2025) Enhanced iodine adsorption performance of porous aromatic frameworks from nitrogen-containing monomers. Sep Purif Technol 370:133230. https://doi.org/10.1016/j.seppur.2025.13323010.1016/j.seppur.2025.133230 ↗
91. Zhang J, Wang X, Guo X, Sang W, He Q, Zhang W (2025) Crystal- and pore-size dependent iodine adsorption properties in MOFs. Small 21:2410678. https://doi.org/10.1002/smll.20241067810.1002/smll.202410678 ↗
92. Li L, Yang G, Wang Y (2025) Efficient iodine adsorption from water using tailored multi-heteroatom porous metal–organic framework by dual-ligand strategy. Sep Purif Technol 370:133227. https://doi.org/10.1016/j.seppur.2025.13322710.1016/j.seppur.2025.133227 ↗
93. Bi J, Bao K, Zhao M et al (2025) Novel phenol-functionalized hypercrosslinked polymer for efficient tetracycline and iodine adsorption. Appl Surf Sci 688:162385. https://doi.org/10.1016/j.apsusc.2025.16238510.1016/j.apsusc.2025.162385 ↗
94. Zheng Z, Lin Q, Gao Y, Ji X, Sessler JL, Wang H (2024) Recent advances in iodine adsorption from water. Coord Chem Rev 511:215860. https://doi.org/10.1016/j.ccr.2024.21586010.1016/j.ccr.2024.215860 ↗
95. Sedov I, Magsumov T, Abdullin A et al (2018) Influence of the cross-link density on the rate of crystallization of poly (ε-caprolactone). Polymers 10:90210.3390/polym10080902 ↗
96. Geng T-M, Liu M, Hu C, Zhu F (2021) Flexible oxygen-bridged porous organic polymers for adsorping and fluorescence sensing iodine and the formation of liquid complexes of POPs-(poly) iodide anions. Macromol Mater Eng 306(4):2000711. https://doi.org/10.1002/mame.20200071110.1002/mame.202000711 ↗
97. Khosravi Esmaeiltarkhani F, Dinari M, Mokhtari N (2024) Nitrogen-rich porous organic polymer as a promising adsorbent for iodine capture from organic solvents. New J Chem 48:1943. https://doi.org/10.1039/D3NJ04674E10.1039/D3NJ04674E ↗
98. Xie Y, Pan T, Lei Q et al (2022) Efficient and simultaneous capture of iodine and methyl iodide achieved by a covalent organic framework. Nat Commun 13:2878. https://doi.org/10.1038/s41467-022-30663-310.1038/s41467-022-30663-3 ↗
99. Hassan A, Mondal S, Wahed SA et al (2025) Influence on crystallinity of nanoporous covalent organic frameworks for efficient sequestration of organic iodides and iodine. ACS Appl Nano Mater 8:12895. https://doi.org/10.1021/acsanm.5c0146310.1021/acsanm.5c01463 ↗