Читать книгу Poly(lactic acid) - Группа авторов - Страница 59
REFERENCES
Оглавление1 1. D. R. Witzke, Introduction to properties, engineering, and prospects of polylactide polymers, Ph.D. thesis, Michigan State University, East Lansing, 1997.
2 2. W. D. Bancroft, H. L. Davis, The optical rotation of lactic acid, J. Phys. Chem. 1931, 35(9), 2508–2529.
3 3. H. Henry, N. Marmy Conus, P. Steenhout, Béguin A, Boulat O., Sensitive determination of d‐lactic acid and l‐lactic acid in urine by high‐performance liquid chromatography‐tandem mass spectrometry: d‐lactic acid and l‐lactic acid in urine, Biomed. Chromatogr. 2012, 26(4), 425–428.
4 4. X. Ding, S. Lin, H. Weng, J. Liang, Separation and determination of the enantiomers of lactic acid and 2‐hydroxyglutaric acid by chiral derivatization combined with gas chromatography and mass spectrometry, J. Sep. Sci. 2018, 41(12), 2576–2584.
5 5. L. Zhang, A. F. Martins, P. Zhao, M. Tieu, D. Esteban‐Gómez, G. T. McCandless, et al., Enantiomeric recognition of d‐ and l‐lactate by CEST with the aid of a paramagnetic shift reagent, J. Am. Chem. Soc. 2017, 139(48), 17431–17437.
6 6. H. Borsook, H. M. Huffman, Y.‐P. Liu, The preparation of crystalline lactic acid, J. Biol. Chem. 1933, 102(2), 449–460.
7 7. V. L. Novikov, O. P. Shestak, Reactions of hydrogen peroxide with acetylacetone and 2‐acetylcyclopentanone, Russ. Chem. Bull. 2013, 62(10), 2171–2190.
8 8. J. Schott, J. Kretzschmar, S. Tsushima, B. Drobot, M. Acker, A. Barkleit, et al., The interaction of Eu(III) with organoborates—a further approach to understand the complexation in the An/Ln(III)–borate system, Dalton Trans. 2015, 44(24), 11095–11108.
9 9. C. T. Bowmer, R. N. Hooftman, A. O. Hanstveit, P. W. M. Venderbosch, N. van der Hoeven, The ecotoxicity and the biodegradability of lactic acid, alkyl lactate esters and lactate salts, Chemosphere 1998, 37(7), 1317–1333.
10 10. K. Masutani, Y. Kimura, Chapter 1. PLA synthesis. From the monomer to the polymer, in: A. Jiménez, M. Peltzer, R. Ruseckaite (Eds.), Polymer Chemistry Series [Internet], Royal Society of Chemistry, Cambridge, 2014 [cited 31 March 2021], pp. 1–36. Available from: http://ebook.rsc.org/?DOI=10.1039/9781782624806‐00001.
11 11. Feng L, X. Bian, Z. Chen, S. Xiang, Y. Liu, B. Sun, et al., Determination of d‐lactide content in lactide stereoisomeric mixture using gas chromatography‐polarimetry, Talanta 2017, 164, 268–274.
12 12. M. Muller, J. Hess, W.‐G. Schnell, G. Entenmann, Meso‐lactide, processes for preparing it and polymers and copolymers produced therefrom, US Patent 4,983,745, 1991.
13 13. H. Rinderknecht, C. Niemann, The esterification of acylated α‐amino acids, J. Am. Chem. Soc. 1948, 70(7), 2605–2606.
14 14. B. Iselin, E. A. Zeller, 196. Über den enzymatischen Abbau von l‐α‐oxysäuren, Helv. Chim. Acta. 1946, 29(6), 1508–1520. https://dx.doi.org/10.1002/hlca.19460290618.
15 15. A. Šepitka, Physical‐technical properties of lactic acid, Pru˚m. Potravin. 1961, 12, 661–665.
16 16. E. Cherbuliez, H. Weniger, 255. Phosphorylations par les acides polyphosphoriques, Helv. Chim. Acta. 1946, 29(6), 2006–2017.
17 17. V. V. Perekalin, A. K. Petryaeva, M. M. Zobacheva, É. L. Metelkina, New method of synthesizing α‐hydroxy and α‐ketoacids, Dokl. Chem. 1966, 166, 217–219.
18 18. V. Ababi, A. Popa, Studiul echilibrului sistemului ternar: acid lactic—apă—solvent organic, Analele Stiitifice Univ. Al Cuza Sect. I. 1960, 6, 929–942.
19 19. G. Losse, G. Bachmann, Synthese von depsipeptiden, Chem. Ber. 1964, 97(9), 2671–2680.
20 20. D. Vorländer, R. Walter, Die mechanisch erzwungene Doppelbrechung der amorphen Flüssigkeiten im Zusammenhang mit der molekularen Gestalt, Z. Für. Phys. Chem. 1925, 118U(1), 1–30.
21 21. Y. Ogata, M. Inaishi, Preparation of dl‐alanine by the reaction of (±)‐2‐chloropropionic acid with aqueous ammonia under pressure, Bull. Chem. Soc. Jpn. 1981, 54(11), 3605–3606.
22 22. P. J. Flory, Molecular size distribution in linear condensation polymers, J. Am. Chem. Soc. 1936, 58(10), 1877–1885.
23 23. P. D. Watson, Composition of lactic acid production of a highly concentrated acid, Ind. Eng. Chem. 1940, 32(3), 399–401.
24 24. R. Montgomery, Acidic constituents of lactic acid‐water systems, J. Am. Chem. Soc. 1952, 74(6), 1466–1468.
25 25. R. Ueda, T. Terajima, The utilization of lactic acid obtained by fermentation, XII. Change in the polymers by dilution with water, Hakko Kogaku Zasshi. 1958, 36, 371–374.
26 26. S. Bezzi, L. Riccoboni, Memorie della Classe di Scienze Fisiche, Matematiche e Naturali. Reale Accademia d'Italia 1937, 8, 181–200.
27 27. D. T. Vu, A. K. Kolah, N. S. Asthana, L. Peereboom, C. T. Lira, D. J. Miller, Oligomer distribution in concentrated lactic acid solutions, Fluid Phase Equilibria. 2005, 236(1–2), 125–135.
28 28. C. H. Holten, A. Müller, D. Rehbinde, Lactic Acid, Verlag Chemie, International Research Association, Copenhagen, 1971.
29 29. S. Feng, S. Xiang, X. Bian, G. Li, Quantitative analysis of total acidity in aqueous lactic acid solutions by direct potentiometric titration, Microchem. J. 2020, 157, 105049.
30 30. M. T. Sanz, S. Beltran, B. Calvo, J. L. Cabezas, Vapor liquid equilibria of the mixtures involved in the esterfication of lactic acid with methanol, J. Chem. Eng. Data. 2003, 48(6), 1446–1452.
31 31. D. T. Vu, Properties and separations of plant‐derived chemicals, Ph.D. thesis, Michigan State University, East Lansing 2007.
32 32. R. A. Troupe, W. L. Aspy, P. R. Schrodt, Viscosity and density of aqueous lactic acid solutions, Ind. Eng. Chem. 1951, 43(5), 1143–1146.