Choline Chloride-based Deep Eutectic Solvents for Degradation of Waste Cotton Fibrics to 5-Hydroxymethylfurfural
Source abstract
Abstract
The preparation of value-added products is an effective way to reuse waste cotton fabrics (WCFs). Seven kinds of choline chloride (ChCl)-based deep eutectic solvents (DESs) were rapidly formed and characterized. Performances of these ChCl-based DESs were evaluated in terms of degradation of WCFs to 5-hydroxymethylfurfural (5-HMF) without any additional catalyst. The degradation was characterized by high-performance liquid chromatography (HPLC) and scanning electron microscopy (SEM) method. The results showed that the DESs formed by ChCl and p-toluene sulfonic acid (p-TSA) had the best effect in converting WCFs. Moreover, the stability of 5-HMF in the as-obtained DESs was also investigated. The highest 5-HMF yield was 10.20 % at 100 °C, with a reaction time of 90 min, and the molar ratio of hydrogen bond acceptor (HBA) to hydrogen bond donor (HBD) was 1:1.3 in ChCl/p-TSA DESs system without a catalyst. The investigated DESs system offers a good alternative compared to the available WCFs degradation methods, considering its cost-efficiency, environmental, and operability aspects. Therefore, the green and environmentally friendly synthesis of 5-HMF from cellulose materials (WCFs) could be an effective method to realize the high-value utilization of waste textiles, having an important theoretical significance and practical value.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Catalysis for Biomass Conversion · Lignin and Wood Chemistry · Ionic liquids properties and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (43)
Show source-provided references
1. China Textile Industry Federation, “2018/2019 China Textile Industry Development Report”, pp.6–7, China Textile & Apparel Press, Beijing, 2019.
2. R. Xiong, X. X. Zhang, D. Tian, Z. H. Zhou, and C. H. Lu, Cellulose, 19, 1189 (2012).10.1007/s10570-012-9730-4 ↗
3. S. Nikolić, V. Lazić, D. Veljović, and L. Mojović, Carbohydr. Polym., 164, 136 (2017).10.1016/j.carbpol.2017.01.090 ↗
4. A. S. Khan, Z. Man, M. A. Bustam, C. F. Kait, A. Nasrullah, Z. Ullah, A. Sarwono, P. Ahamd, and N. Muhammad, J. Cleaner Prod., 170, 591 (2018).10.1016/j.jclepro.2017.09.103 ↗
5. C. O. Tuck, E. Pérez, I. T. Horváth, R. A. Sheldon, and M. Poliakoff, Science, 337, 695 (2012).10.1126/science.1218930 ↗
6. S. M. Notley and L. Wågberg, Biomacromolecules, 6, 1586 (2005).10.1021/bm050005u ↗
7. B. Hinterstoisser and L. Salmén, Vib. Spectrosc., 22, 111 (2000).10.1016/S0924-2031(99)00063-6 ↗
8. H. Q. Wang, J. C. Li, X. H. Zeng, X. Tang, Y. Sun, T. Z. Lei, and L. Lin, Cellulose, 27, 1301 (2019).10.1007/s10570-019-02867-2 ↗
9. K. Saalwächter, W. Burchard, P. Klüfers, G. Kettenbach, P. Mayer, D. Klemm, and S. Dugarmaa, Macromolecules, 33, 4094 (2000).10.1021/ma991893m ↗
10. T. Heinze and A. Koschella, Polímeros: Ciência e Tecnologia, 15, 84 (2005).10.1590/S0104-14282005000200005 ↗
11. G. Y. Ru, H. Luo, X. M. Liang, L. Y. Wang, C. Y. Liu, and J. W. Feng, Cellulose, 22, 2221 (2015).10.1007/s10570-015-0667-2 ↗
12. H. S. Qi, J. Cai, L. N. Zhang, and S. Kuga, Biomacromolecules, 10, 1597 (2009).10.1021/bm9001975 ↗
13. J. Cai and L. Zhang, Macromol. Biosci., 5, 539 (2005).10.1002/mabi.200400222 ↗
14. D. L. Minnick, R. A. Flores, M. R. DeStefano, and A. M. Scurto, J. Phys. Chem. B, 120, 7906 (2016).10.1021/acs.jpcb.6b04309 ↗
15. Y. Tomimatsu, H. Suetsugu, Y. Yoshimura, and A. Shimizu, J. Mol. Liq., 279, 120 (2019).10.1016/j.molliq.2019.01.093 ↗
16. R. P. Swatloski, S. K. Spear, J. D. Holbrey, and R. D. Rogers, J. Am. Chem. Soc., 124, 4974 (2002).10.1021/ja025790m ↗
17. H. Zhang, S. X. Li, X. Song, P. F. Li, and J. X. Li, Bioresources, 11, 5190 (2016).
18. H. B. Zhao, J. E. Holladay, H. Brown, and Z. C. Zhang, Science, 316, 1597 (2007).10.1126/science.1141199 ↗
19. H. Zhao, Phy. Chem. Liq., 41, 545 (2003).10.1080/003191031000117319 ↗
20. A. P. Abbott, G. Capper, D. L. Davies, R. K. Rasheed, and V. Tambyrajah, Chem. Commun. (Camb), 70 (2003).10.1039/b210714g ↗
21. K. D. O. Vigier, G. Chatel, and F. Jerome, ChemCatChem, 7, 1250 (2015).10.1002/cctc.201500134 ↗
22. M. H. Shafie, R. Yusof, and C. Y. Gan, J. Mol. Liq., 288, 111081 (2019).10.1016/j.molliq.2019.111081 ↗
23. E. L. Smith, A. P. Abbott, and K. S. Ryder, Chem. Rev., 114, 11060 (2014).10.1021/cr300162p ↗
24. A. P. Abbott, G. Capper, D. L. Davies, K. J. McKenzie, and S. U. Obi, J. Chem. Eng. Data, 51, 1280 (2006).10.1021/je060038c ↗
25. A. Hayyan, F. S. Mjalli, I. M. AlNashef, T. Al-Wahaibi, Y. M. Al-Wahaibi, and M. A. Hashim, Thermochimi. Acta, 541, 70 (2012).10.1016/j.tca.2012.04.030 ↗
26. L. Segal, J. J. Creely, A. E. Martin, and C. M. Conrad, Text. Res. J., 29, 786 (1959).10.1177/004051755902901003 ↗
27. M. A. Kareem, F. S. Mjalli, M. A. Hashim, and I. M. AINashef, J. Chem. Eng. Data, 55, 4632 (2010).10.1021/je100104v ↗
28. M. K. Alomar, M. Hayyan, M. A. Alsaadi, S. Akib, A. Hayyan, and M. A. Hashim, J. Mol. Liq., 215, 98 (2016).10.1016/j.molliq.2015.11.032 ↗
29. W. J. Chen, J. Y. Jiang, X. Lan, X. H. Zhao, H. Y. Mou, and T. C. Mu, Green Chem., 21, 4748 (2019).10.1039/C9GC00944B ↗
30. K. C. Badgujar and B. M. Bhanage, Bioresour. Technol., 178, 2 (2015).10.1016/j.biortech.2014.09.138 ↗
31. Y. Z. Liu, B. T. Guo, Q. Q. Xia, J. Meng, W. S. Chen, S. X. Liu, Q. W. Wang, Y. X. Liu, J. Li, and H. P. Yu, ACS Sustain. Chem. Eng., 5, 7623 (2017).10.1021/acssuschemeng.7b00954 ↗
32. A. P. Abbott, T. J. Bell, S. Handa, and B. Stoddart, Green Chem., 8, 784 (2006).10.1039/b605258d ↗
33. S. T. Disale, S. R. Kale, S. S. Kahandal, T. G. Srinivasan, and R. V. Jayaram, Tetrahedron Lett., 53, 2277 (2012).10.1016/j.tetlet.2012.02.054 ↗
34. A. R. Hajipour, S. H. Nazemzadeh, and F. Mohammadsaleh, Tetrahedron Lett., 55, 654 (2014).10.1016/j.tetlet.2013.11.105 ↗
35. F. J. Liu, Z. M. Xue, X. H. Zhao, H. Y. Mou, J. He, and T. C. Mu, Chem. Commun., 54, 6140 (2018).10.1039/C8CC03798A ↗
36. F. Liu, J. Barrault, K. D. O. Vigier, and F. Jerome, ChemSusChem, 5, 1223 (2012).10.1002/cssc.201200186 ↗
37. J. T. Gorke, F. Srienc, and R. J. Kazlauskas, Chem. Commun. (Camb), 10, 1235 (2008).10.1039/b716317g ↗
38. L. Cammarata, S. G. Kazarian, P. A. Salter, and T. Welton, Phys. Chem. Chem. Phys., 3, 5192 (2001).10.1039/b106900d ↗
39. L. Yan, A. A. Greenwood, A. Hossain, and B. Yang, RSC Adv., 4, 23492 (2014).10.1039/c4ra01631a ↗
40. S. K. R. Patil and C. R. F. Lund, Energ. Fuel., 25, 4745 (2011).10.1021/ef2010157 ↗
41. Q. Zhao, L. Wang, S. Zhao, X. H. Wang, and S. T. Wang, Fuel, 90, 2289 (2011).10.1016/j.fuel.2011.02.022 ↗
42. Z. S. Yuan, C. B. Xu, S. N. Cheng, and M. Leitch, Carbohydr. Res., 346, 2019 (2011).10.1016/j.carres.2011.06.007 ↗
43. A. A. Assanosi, M. M. Farah, J. Wood, and B. Al-Duri, RSC Adv., 4, 39359 (2014).10.1039/C4RA07065H ↗