[1]
Staples, C. A.; Dome, P. B.; Klecka, G. M.; Oblock, S. T.; Harris, L. R. A review of the environmental fate, effects, and exposures of bisphenol A. Chemosphere 1998, 36, 2149-2173.
[2]
Fu, P. Q.; Kawamura, K. Ubiquity of bisphenol A in the atmosphere. Environ. Pollut. 2010, 158, 3138-3143.
[3]
Ben-Jonathan, N.; Hugo, E. R.; Brandebourg, T. D. Effects of bisphenol A on adipokine release from human adipose tissue: Implications for the metabolic syndrome. Mol. Cell. Endocrinol. 2009, 304, 49-54.
[4]
Boucher, J. G.; Boudreau, A.; Atlas, E. Bisphenol A induces differentiation of human preadipocytes in the absence of glucocorticoid and is inhibited by an estrogen-receptor antagonist. Nutr. Diabetes 2014, 4, e102.
[5]
Héliès-Toussaint, C.; Peyre, L.; Costanzo, C.; Chagnon, M. C.; Rahmani, R. Is bisphenol S a safe substitute for bisphenol A in terms of metabolic function? An in vitro study. Toxicol. Appl. Pharmacol. 2014, 280, 224-235.
[6]
Arampatzidou, A.; Voutsa, D.; Deliyanni, E. Removal of bisphenol A by Fe-impregnated activated carbons. Environ. Sci. Pollut. Res. 2018, 25, 25869-25879.
[7]
Crini, G. Recent developments in polysaccharide-based materials used as adsorbents in wastewater treatment. Prog. Polym. Sci. 2005, 30, 38-70.
[8]
Zhang, H.; Wang, H.; Wang, F. F.; Wei, J. F.; Zhou, X. Y.; Ji, Y. L. Fabrication of hydrophilic and hydrophobic site on polypropylene nonwoven for removal of bisphenol A from water: Explorations on adsorption behaviors, mechanisms and configurational influence. J. Polym. Res. 2017, 24, 171.
[9]
Ali, I.; Gupta, V. K. Advances in water treatment by adsorption technology. Nat. Protoc. 2006, 1, 2661-2667.
[10]
Bhatnagar, A.; Anastopoulos, I. Adsorptive removal of bisphenol A (BPA) from aqueous solution: A review. Chemosphere 2017, 168, 885-902.
[11]
Katsigiannis, A.; Noutsopoulos, C.; Mantziaras, J.; Gioldasi, M. Removal of emerging pollutants through granular activated carbon. Chem. Eng. J. 2015, 280, 49-57.
[12]
Paredes, L.; Alfonsin, C.; Allegue, T.; Omil, F.; Carballa, M. Integrating granular activated carbon in the post-treatment of membrane and settler effluents to improve organic micropollutants removal. Chem. Eng. J. 2018, 345, 79-86.
[13]
Chiang, P. C.; Chang, E. E.; Wu, J. S. Comparison of chemical and thermal regeneration of aromatic compounds on exhausted activated carbon. Water Sci. Technol. 1997, 35, 279-285.
[14]
San Miguel, G.; Lambert, S. D.; Graham, N. J. D. The regeneration of field-spent granular-activated carbons. Water Res. 2001, 35, 2740-2748.
[15]
Bautista-Toledo, I.; Ferro-García, M. A.; Rivera-Utrilla, J.; Moreno-Castilla, C.; Vegas Fernández, F. J. Bisphenol A removal from water by activated carbon. Effects of carbon characteristics and solution chemistry. Environ. Sci. Technol. 2005, 39, 6246-6250.
[16]
Wang, S. B.; Peng, Y. L. Natural zeolites as effective adsorbents in water and wastewater treatment. Chem. Eng. J. 2010, 156, 11-24.
[17]
Shen, Y. H. Phenol sorption by organoclays having different charge characteristics. Colloids Surf. A: Physicochem. Eng. Aspects 2004, 232, 143-149.
[18]
Li, J.; Zhan, Y. H.; Lin, J. W.; Jiang, A.; Xi, W. Removal of bisphenol A from aqueous solution using cetylpyridinium bromide (CPB)-modified natural zeolites as adsorbents. Environ. Earth Sci. 2014, 72, 3969-3980.
[19]
Xu, J.; Wang, L.; Zhu, Y. F. Decontamination of bisphenol A from aqueous solution by graphene adsorption. Langmuir 2012, 28, 8418-8425.
[20]
Fang, Z.; Hu, Y. Y.; Wu, X. S.; Qin, Y. Z.; Cheng, J. H.; Chen, Y. C.; Tan, P.; Li, H. Q. A novel magnesium ascorbyl phosphate graphene-based monolith and its superior adsorption capability for bisphenol A. Chem. Eng. J. 2018, 334, 948-956.
[21]
Fang, Z.; Hu, Y. Y.; Zhang, W. W.; Ruan, X. Shell-free three-dimensional graphene-based monoliths for the aqueous adsorption of organic pollutants. Chem. Eng. J. 2017, 316, 24-32.
[22]
Wang, P.; Xiao, P. Y.; Zhong, S. X.; Chen, J. R.; Lin, H. J.; Wu, X. L. Bamboo-like carbon nanotubes derived from colloidal polymer nanoplates for efficient removal of bisphenol A. J. Mater. Chem. A 2016, 4, 15450-15456.
[23]
Kuo, C. Y. Comparison with as-grown and microwave modified carbon nanotubes to removal aqueous bisphenol A. Desalination 2009, 249, 976-982.
[24]
Jun, L. Y.; Mubarak, N. M.; Yee, M. J.; Yon, L. S.; Bing, C. H.; Khalid, M.; Abdullah, E. C. An overview of functionalised carbon nanomaterial for organic pollutant removal. J. Ind. Eng. Chem. 2018, 67, 175-186.
[25]
Xiao, G. Q.; Fu, L. C.; Li, A. M. Enhanced adsorption of bisphenol A from water by acetylaniline modified hyper-cross-linked polymeric adsorbent: Effect of the cross-linked bridge. Chem. Eng. J. 2012, 191, 171-176.
[26]
Park, E. Y.; Hasan, Z.; Khan, N. A.; Jhung, S. H. Adsorptive removal of bisphenol A from water with a metal-organic framework, a porous chromium-benzenedicarboxylate. J. Nanosci. Nanotechnol. 2013, 13, 2789-2794.
[27]
Zhou, M. M.; Wu, Y. N.; Qiao, J. L.; Zhang, J.; McDonald, A.; Li, G. T.; Li, F. T. The removal of bisphenol A from aqueous solutions by MIL-53(Al) and mesostructured MIL-53(Al). J. Colloid Interface Sci. 2013, 405, 157-163.
[28]
Liu, Y.; Zhong, G. X.; Liu, Z. C.; Meng, M. J.; Liu, F. F.; Ni, L. Facile synthesis of novel photoresponsive mesoporous molecularly imprinted polymers for photo-regulated selective separation of bisphenol A. Chem. Eng. J. 2016, 296, 437-446.
[29]
Asada, T.; Oikawa, K.; Kawata, K.; Ishihara, S.; Iyobe, T.; Yamada, A. Study of removal effect of bisphenol A and β-estradiol by porous carbon. J. Health Sci. 2004, 50, 588-593.
[30]
Krause, R. W.; Mamba, B. B.; Bambo, F. M.; Malefetse, T. J. Cyclodextrin polymers: Synthesis and application in water treatment. In Cyclodextrins: Chemistry and Physics; Hu, J., Ed.; Transworld Research Network: Kerala, India, 2010; pp 185-210.
[31]
Morin-Crini, N.; Crini, G. Environmental applications of water-insoluble β-cyclodextrin-epichlorohydrin polymers. Prog. Polym. Sci. 2013, 38, 344-368.
[32]
Sikder, M. T.; Rahman, M. M.; Jakariya, M.; Hosokawa, T.; Kurasaki, M.; Saito, T. Remediation of water pollution with native cyclodextrins and modified cyclodextrins: A comparative overview and perspectives. Chem. Eng. J. 2019, 355, 920-941.
[33]
Gidwani, B.; Vyas, A. Synthesis, characterization and application of epichlorohydrin-β-cyclodextrin polymer. Colloids Surf. B: Biointerfaces 2014, 114, 130-137.
[34]
Yang, Z. X.; Chen, Y.; Liu, Y. Inclusion complexes of bisphenol A with cyclomaltoheptaose (β-cyclodextrin): Solubilization and structure. Carbohydr. Res. 2008, 343, 2439-2442.
[35]
Morin-Crini, N.; Winterton, P.; Fourmentin, S.; Wilson, L. D.; Fenyvesi, É.; Crini, G. Water-insoluble β-cyclodextrin-epichlorohydrin polymers for removal of pollutants from aqueous solutions by sorption processes using batch studies: A review of inclusion mechanisms. Prog. Polym. Sci 2018, 78, 1-23.
[36]
Liu, H. H.; Cai, X. Y.; Wang, Y.; Chen, J. W. Adsorption mechanism-based screening of cyclodextrin polymers for adsorption and separation of pesticides from water. Water Res. 2011, 45, 3499-3511.
[37]
Wang, Z. H.; Zhang, P. B.; Hu, F.; Zhao, Y. F.; Zhu, L. P. A crosslinked β-cyclodextrin polymer used for rapid removal of a broad-spectrum of organic micropollutants from water. Carbohydr. Polym. 2017, 177, 224-231.
[38]
Morales-Sanfrutos, J.; Lopez-Jaramillo, F. J.; Elremaily, M. A. A.; Hernández-Mateo, F.; Santoyo-Gonzalez, F. Divinyl sulfone cross-linked cyclodextrin-based polymeric materials: Synthesis and applications as sorbents and encapsulating agents. Molecules 2015, 20, 3565-3581.
[39]
Kono, H.; Nakamura, T. Polymerization of β-cyclodextrin with 1,2,3,4-butanetetracarboxylic dianhydride: Synthesis, structural characterization, and bisphenol A adsorption capacity. React. Funct. Polym. 2013, 73, 1096-1102.
[40]
Tang, P. X.; Sun, Q. M.; Suo, Z. L.; Zhao, L. D.; Yang, H. Q.; Xiong, X. N.; Pu, H. Y.; Gan, N.; Li, H. Rapid and efficient removal of estrogenic pollutants from water by using beta- and gamma-cyclodextrin polymers. Chem. Eng. J. 2018, 344, 514-523.
[41]
Alsbaiee, A.; Smith, B. J.; Xiao, L. L.; Ling, Y. H.; Helbling, D. E.; Dichtel, W. R. Rapid removal of organic micropollutants from water by a porous β-cyclodextrin polymer. Nature 2016, 529, 190-194.
[42]
De Souza, Í. F. T.; Petri, D. F. S. β-Cyclodextrin hydroxypropyl methylcellulose hydrogels for bisphenol A adsorption. J. Mol. Liq. 2018, 266, 640-648.
[43]
Liu, J.; Yang, Y. M.; Bai, J. W.; Wen, H.; Chen, F. J.; Wang, B. D. Hyper-cross-linked porous MoS2-cyclodextrin-polymer frameworks: Durable removal of aromatic phenolic micropollutant from water. Anal. Chem. 2018, 90, 3621-3627.
[44]
Li, X. M.; Zhou, M. J.; Jia, J. X.; Ma, J. T.; Jia, Q. Design of a hyper-crosslinked β-cyclodextrin porous polymer for highly efficient removal toward bisphenol A from water. Sep. Purif. Technol. 2018, 195, 130-137.
[45]
Kumprecht, L.; Buděšínský, M.; Vondrášek, J.; Vymětal, J.; Černý, J.; Císařová, I.; Brynda, J.; Herzig, V.; Koutník, P.; Závada, J. et al. Rigid duplex α-cyclodextrin reversibly connected with disulfide bonds. Synthesis and inclusion complexes. J. Org. Chem. 2009, 74, 1082-1092.
[46]
Liu, Y.; Chen, Y. Cooperative binding and multiple recognition by bridged bis(β-cyclodextrin)s with functional linkers. Acc. Chem. Res. 2006, 39, 681-691.
[47]
Breslow, R.; Greenspoon, N.; Guo, T.; Zarzycki, R. Very strong binding of appropriate substrates by cyclodextrin dimers. J. Am. Chem. Soc. 1989, 111, 8296-8297.
[48]
Harada, A.; Furue, M.; Nozakura, S. I. Cooperative binding by cyclodextrin dimers. Polym. J. 1980, 12, 29-33.
[49]
Liu, Y.; You, C. C.; Zhang, H. Y.; Kang, S. Z.; Zhu, C. F.; Wang, C. Bis(molecular tube)s: Supramolecular assembly of complexes of organoselenium-bridged β-cyclodextrins with platinum(IV). Nano Lett. 2001, 1, 613-616.
[50]
Liu, Y.; Yang, Z. X.; Chen, Y.; Song, Y.; Shao, N. Construction of a long cyclodextrin-based bis(molecular tube) from bis(polypseudorotaxane) and its capture of C60. ACS Nano 2008, 2, 554-560.
[51]
Furukawa, Y.; Ishiwata, T.; Sugikawa, K.; Kokado, K.; Sada, K. Nano- and microsized cubic gel particles from cyclodextrin metal-organic frameworks. Angew. Chem., Int. Ed. 2012, 51, 10566-10569.
[52]
Tao, Y. X.; Gu, X. G.; Deng, L. H.; Qin, Y.; Xue, H. G.; Kong, Y. Chiral recognition of D-tryptophan by confining high-energy water molecules inside the cavity of copper-modified β-cyclodextrin. J. Phys. Chem. C 2015, 119, 8183-8190.
[53]
Shih, Y. H.; Kuo, Y. C.; Lirio, S.; Wang, K. Y.; Lin, C. H.; Huang, H. Y. A simple approach to enhance the water stability of a metal-organic framework. Chem.—Eur. J. 2017, 23, 42-46.
[54]
Hartlieb, K. J.; Holcroft, J. M.; Moghadam, P. Z.; Vermeulen, N. A.; Algaradah, M. M.; Nassar, M. S.; Botros, Y. Y.; Snurr, R. Q.; Stoddart, J. F. Cd-MOF: A versatile separation medium. J. Am. Chem. Soc. 2016, 138, 2292-2301.
[55]
Wang, L.; Liang, X. Y.; Chang, Z. Y.; Ding, L. S.; Zhang, S.; Li, B. J. Effective formaldehyde capture by green cyclodextrin-based metal-organic framework. ACS Appl. Mater. Interfaces 2018, 10, 42-46.
[56]
Sha, J. Q.; Zhong, X. H.; Wu, L. H.; Liu, G. D.; Sheng, N. Nontoxic and renewable metal-organic framework based on α-cyclodextrin with efficient drug delivery. RSC Advances 2016, 6, 82977-82983.
[57]
Wu, Y. L.; Shi, R. F.; Wu, Y. L.; Holcroft, J. M.; Liu, Z. C.; Frasconi, M.; Wasielewski, M. R.; Li, H.; Stoddart, J. F. Complexation of polyoxometalates with cyclodextrins. J. Am. Chem. Soc. 2015, 137, 4111-4118.
[58]
Holcroft, J. M.; Hartlieb, K. J.; Moghadam, P. Z.; Bell, J. G.; Barin, G.; Ferris, D. P.; Bloch, E. D.; Algaradah, M. M.; Nassar, M. S.; Botros, Y. Y. et al. Carbohydrate-mediated purification of petrochemicals. J. Am. Chem. Soc. 2015, 137, 5706-5719.
[59]
Singh, V.; Guo, T.; Xu, H. T.; Wu, L.; Gu, J. K.; Wu, C. B.; Gref, R.; Zhang, J. W. Moisture resistant and biofriendly Cd-MOF nanoparticles obtained via cholesterol shielding. Chem. Commun. 2017, 53, 9246-9249.
[60]
Li, H. Q.; Hill, M. R.; Huang, R. H.; Doblin, C.; Lim, S.; Hill, A. J.; Babarao, R.; Falcaro, P. Facile stabilization of cyclodextrin metal-organic frameworks under aqueous conditions via the incorporation of C60 in their matrices. Chem. Commun. 2016, 52, 5973-5976.
[61]
Yamasaki, H.; Makihata, Y.; Fukunaga, K. Efficient phenol removal of wastewater from phenolic resin plants using crosslinked cyclodextrin particles. J. Chem. Technol. Biotechnol. 2006, 81, 1271-1276.
[62]
Klemes, M. J.; Ling, Y. H.; Chiapasco, M.; Alsbaiee, A.; Helbling, D. E.; Dichtel, W. R. Phenolation of cyclodextrin polymers controls their lead and organic micropollutant adsorption. Chem. Sci. 2018, 9, 8883-8889.
[63]
García-Zubiri, I. X.; González-Gaitano, G.; Isasi, J. R. Sorption models in cyclodextrin polymers: Langmuir, Freundlich, and a dual-mode approach. J. Colloid Interface Sci. 2009, 337, 11-18.
[64]
Huang, Y. Q.; Wong, C. K. C.; Zheng, J. S.; Bouwman, H.; Barra, R.; Wahlström, B.; Neretin, L.; Wong, M. H. Bisphenol A (BPA) in China: A review of sources, environmental levels, and potential human health impacts. Environ. Int. 2012, 42, 91-99.
[65]
Huey, R.; Morris, G. M.; Olson, A. J.; Goodsell, D. S. A semiempirical free energy force field with charge-based desolvation. J. Comput. Chem. 2007, 28, 1145-1152.
AI Chat Paper
