Amphiphilic Copolymers Derived from Butanosolv Lignin and Acrylamide: Synthesis, Properties in Water Solution, and Potential Applications
Source abstract
Abstract
In this work, a series of amphiphilic lignin-acrylamide copolymers was synthetized via a "grafting from"approach using α-butoxylated organosolv lignin. This lignin is obtained in high yield via a mild organosolv extraction with butanol and contains a well-defined modified β-O-4 structure that allows for site-selective modification of the primary alcohol in the γ-position. The modified lignin was then used as a precursor of amphiphilic copolymers by reaction with acrylamide, either via free radical polymerization or via atom transfer radical polymerization after converting the lignin into a suitable macroinitiator. The effect of the synthetic method and acrylamide/lignin ratio on the final properties was studied and compared. Relevant solution properties, in particular, shear viscosity and interfacial and surface tension, showed that different synthetic methods and polymer compositions allow a tuning of the solution behavior toward specific potential applications, such as emulsion stabilization or enhanced oil recovery. Furthermore, it was preliminarily shown that the obtained polymers may potentially display low cytotoxicity, further increasing the possibilities for applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Lignin and Wood Chemistry · Polymer composites and self-healing · Mesoporous Materials and Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering (ENTEG), University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands
Department of Biomedical Engineering, University of Groningen and University Medical Center Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands
References (69)
Show source-provided references
1. 10.3390/polym1102019210.3390/polym11020192 ↗
2. 10.1016/j.clay.2019.10540510.1016/j.clay.2019.105405 ↗
3. 10.1016/j.carbpol.2019.11506610.1016/j.carbpol.2019.115066 ↗
4. 10.1016/j.carbpol.2019.11538410.1016/j.carbpol.2019.115384 ↗
5. 10.1016/j.carbpol.2007.11.00810.1016/j.carbpol.2007.11.008 ↗
6. 10.1016/j.carbpol.2019.05.08110.1016/j.carbpol.2019.05.081 ↗
7. 10.1016/j.ijbiomac.2017.12.07810.1016/j.ijbiomac.2017.12.078 ↗
8. 10.1016/j.ijbiomac.2019.12.08210.1016/j.ijbiomac.2019.12.082 ↗
9. 10.1016/j.carbpol.2016.08.10110.1016/j.carbpol.2016.08.101 ↗
10. 10.1016/j.apsusc.2018.10.26910.1016/j.apsusc.2018.10.269 ↗
11. 10.1039/B9PY00233B10.1039/B9PY00233B ↗
12. 10.1021/acs.chemrev.5b0024210.1021/acs.chemrev.5b00242 ↗
13. 10.1007/BF0254054110.1007/BF02540541 ↗
14. 10.1021/bm801411w10.1021/bm801411w ↗
15. 10.1016/j.progpolymsci.2016.12.00910.1016/j.progpolymsci.2016.12.009 ↗
16. 10.1021/acs.chemrev.5b0026410.1021/acs.chemrev.5b00264 ↗
17. 10.1039/C9PY01667H10.1039/C9PY01667H ↗
18. 10.1039/C9PY01464K10.1039/C9PY01464K ↗
19. 10.1002/app.4410010.1002/app.44100 ↗
20. 10.1016/j.colsurfa.2017.07.06110.1016/j.colsurfa.2017.07.061 ↗
21. Lora J. H. · 2016
22. 10.1002/pola.2895810.1002/pola.28958 ↗
23. 10.1016/j.reactfunctpolym.2014.09.01710.1016/j.reactfunctpolym.2014.09.017 ↗
24. 10.3390/polym1201008110.3390/polym12010081 ↗
25. 10.1016/j.addr.2008.08.00210.1016/j.addr.2008.08.002 ↗
26. 10.1016/j.ijbiomac.2017.06.03710.1016/j.ijbiomac.2017.06.037 ↗
27. 10.1016/j.seppur.2018.06.04710.1016/j.seppur.2018.06.047 ↗
28. 10.1016/j.clay.2018.02.04810.1016/j.clay.2018.02.048 ↗
29. Wang S. · BioResources · 2016 · 11 · 1765
30. 10.1039/C7GC01812F10.1039/C7GC01812F ↗
31. 10.1016/j.enconman.2017.10.07910.1016/j.enconman.2017.10.079 ↗
32. 10.1016/j.biortech.2015.01.06910.1016/j.biortech.2015.01.069 ↗
33. 10.1016/j.colsurfb.2014.11.01810.1016/j.colsurfb.2014.11.018 ↗
34. 10.1039/C7GC03459H10.1039/C7GC03459H ↗
35. 10.1039/D0GC00661K10.1039/D0GC00661K ↗
36. 10.1039/C5EE01322D10.1039/C5EE01322D ↗
37. 10.1039/D0GC00006J10.1039/D0GC00006J ↗
38. 10.1021/acsomega.9b0137110.1021/acsomega.9b01371 ↗
39. 10.1039/C6GC02739C10.1039/C6GC02739C ↗
40. 10.1021/jf302409d10.1021/jf302409d ↗
41. 10.3390/polym1112191310.3390/polym11121913 ↗
42. 10.1002/cssc.20180197110.1002/cssc.201801971 ↗
43. 10.1039/C6GC02739C10.1039/C6GC02739C ↗
44. 10.1021/acssuschemeng.9b0722210.1021/acssuschemeng.9b07222 ↗
45. 10.1007/s13367-017-0014-210.1007/s13367-017-0014-2 ↗
46. 10.1016/j.petrol.2018.05.00310.1016/j.petrol.2018.05.003 ↗
47. 10.1021/cr500129h10.1021/cr500129h ↗
48. 10.1016/j.fuel.2016.12.07510.1016/j.fuel.2016.12.075 ↗
49. 10.1016/j.proche.2012.06.00210.1016/j.proche.2012.06.002 ↗
50. 10.1515/978311064025010.1515/9783110640250 ↗
51. 10.1021/acs.langmuir.9b0338910.1021/acs.langmuir.9b03389 ↗
52. 10.1016/j.carbpol.2019.11540110.1016/j.carbpol.2019.115401 ↗
53. 10.1016/S1359-0294(96)80118-X10.1016/S1359-0294(96)80118-X ↗
54. 10.1021/ma300565j10.1021/ma300565j ↗
55. 10.1016/j.biteb.2019.10037410.1016/j.biteb.2019.100374 ↗
56. 10.1016/j.pmatsci.2017.12.00110.1016/j.pmatsci.2017.12.001 ↗
57. 10.3390/polym907028010.3390/polym9070280 ↗
58. 10.3390/nano907099710.3390/nano9070997 ↗
59. Zijlstra D. S. · JoVE · 2019 · 143 · e58575
60. 10.1021/acs.iecr.7b0336810.1021/acs.iecr.7b03368 ↗
61. 10.1039/D0GC01209B10.1039/D0GC01209B ↗
62. 10.1080/02773813.2014.93700610.1080/02773813.2014.937006 ↗
63. 10.1002/pola.2480910.1002/pola.24809 ↗
64. 10.1002/anie.20090534010.1002/anie.200905340 ↗
65. 10.1016/j.bej.2012.06.01310.1016/j.bej.2012.06.013 ↗
66. 10.1021/jf060539210.1021/jf0605392 ↗
67. 10.1016/j.jcis.2014.04.04710.1016/j.jcis.2014.04.047 ↗
68. 10.1021/j100804a01010.1021/j100804a010 ↗
69. 10.1007/s11743-000-0113-410.1007/s11743-000-0113-4 ↗