“One-pot” synthesis and characterisation of novel P(3HB)–ethyl cellulose based graft composites through lipase catalysed esterification
文献信息
Hafiz M. N. Iqbal, Godfrey Kyazze, Thierry Tron, Tajalli Keshavarz
In the present study a series of graft composites with poly(3-hydroxybutyrate) (P(3HB) as side chains and ethyl cellulose (EC) as a backbone polymer was successfully synthesised through enzymatic esterification. A range of composites between P(3HB) and EC with different P(3HB) : EC ratios were prepared using lipase as a model catalyst. Subsequently, the resulting composites were then removed from the casting surface under ambient conditions. Finally the target composites were characterised in detail by Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and X-ray diffraction (XRD), and the thermo-mechanical behaviours of the grafted composites were investigated by differential scanning calorimetry (DSC) and dynamic mechanical analyser (DMA) measurements. Whereas, hydrophobic and hydrophilic characteristics were studied through drop contour analysis using water contact angle (WCA) measurements. SEM analyses revealed that the uniform P(3HB) dispersion in the backbone polymer increased the area of P(3HB)–EC contact which further contributed to the efficient functionality of the resulting composites as evidenced by XRD, thermo-mechanical and WCA characterisation profiles of the tested composites. In comparison to the untreated P(3HB) a clear shift in the XRD peaks was observed which clearly indicated the breakdown of some crystalline domains and the regeneration of the amorphous material at a specific region of 2θ values in the case of the grafted composites. Interestingly, untreated P(3HB) was hydrophobic in nature and after lipase treatment P(3HB) and P(3HB)–EC based graft composites attained higher levels of hydrophilicity which is a desired characteristic to enhance the biocompatibility of the materials for proper cell adhesion and proliferation therefore, suggesting P(3HB)–EC as a potential candidate for tissue engineering/bio-medical type applications.
相关文献
Synergy in K+/H+ exchange across phospholipid vesicle membranes with combinations of valinomycin and chlorophenols
James Hudson, Anthony E. G. Cass, B. S. Prabhananda
DOI: 10.1039/B110495K
Active control of product selection in a chemical reaction: a view of the current scene
DOI: 10.1039/B109911F
Probing boundary sites on a Pt/Al2O3 model catalyst by CO2 hydrogenation and in situATR-IR spectroscopy of catalytic solid–liquid interfaces
Davide Ferri, Thomas Bürgi, Alfons Baiker
DOI: 10.1039/B111498K
Laser-induced incandescence and Raman measurements in sooting methane and ethylene flames
DOI: 10.1039/B111335F
EPR spectrum and formation properties of a cubic Rh+ centre in NaCl
H. Vrielinck, F. Callens, P. Matthys
DOI: 10.1039/B110906P
Photophysical properties of [N]phenylenes
C. Dosche, H.-G. Löhmannsröben, A. Bieser, P. I. Dosa, S. Han, M. Iwamoto, A. Schleifenbaum, K. P. C. Vollhardt
DOI: 10.1039/B109342H
Reactions of chemically activated C9H9 species. Part I. The product distribution of the reaction of phenyl radicals with propyne
Luc Vereecken, Holger F. Bettinger, Jozef Peeters
DOI: 10.1039/B109452A
A Mössbauer study of In–Fe2O3/HZSM-5 catalysts for the selective catalytic reduction of NO by methane
Xiaodong Wang, Xuqun Zhao, Jianyi Shen, Xiaoying Sun, Tao Zhang, Liwu Lin
DOI: 10.1039/B110515A
Spectral properties of a fluorescing molecule within a spherical metallic nanocavity
Jörg Enderlein
DOI: 10.1039/B200502F
Laser powered homogeneous pyrolysis of ethyne, propyne, and propadiene initiated by methyl radicals: formation and degradation of hydrocarbons at 800–950 K
Karlheinz Hoyermann, Bettina Jürges
DOI: 10.1039/B111643F
您可能还喜欢
什么是5-Fluoro-4-iodo-2-methylaniline(CAS号:307306-08-7)?
5-氟-4-碘-2-甲氨基苯属于芳香族化合物,其分子式为C8H7FN2I。该化合物具有一定的反应活性,在有机合成和药物化学领域有一定的应用。
4-氟-3-硝基三氟甲苯(CAS号:367-86-2)通常如何合成?
4-氟-3-硝基三氟甲苯通常通过将三氟甲基苯在酸性条件下催化氧化为三氟甲基硝基苯,然后进行氟化反应得到目标化合物。该过程需要使用催化剂,如三氟乙酸,反应产率较高...
6-氯-9-(2,3,5-三苯甲酰氧基-2-C-甲基-beta-D-呋喃核糖基)-9H-嘌呤(CAS号:205171-05-7)的物理化学性质是什么?
该化合物为白色至类白色晶体,分子量约为1046.95。它在水中几乎不溶,在有机溶剂如乙腈和甲醇中具有一定的溶解性。该化合物具有良好的化学稳定性和生物活性。
如何储存6-氟喹啉-4-羧酸(CAS号:220844-73-5)?
6-氟喹啉-4-羧酸应储存在阴凉、干燥、通风良好的地方,避免阳光直射。储存在密闭容器中,避免与空气中的水分接触。储存温度应控制在室温以下,避免高温。
(2S,2'S,3S,3'S)-3,3'-di-tert-butyl-4,4'-bis(2,6-dimethoxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole(CAS号:1435940-21-8)通常如何合成?
该化合物通常通过芳香族化合物的亲核取代反应合成,首先将2,6-二甲氧基苯基引入到双环结构中,然后通过特定条件下的还原或氧化反应引入二叔丁基。反应过程中使用了钯作...
如何储存KY02111(CAS号:1118807-13-8)?
KY02111应储存于阴凉、干燥、通风良好的地方,避免阳光直射和高温环境。应使用合适的密闭容器储存,并确保容器密封良好,防止水分和潮气进入。在储存期间,应注意检...
如何储存4-(4-氯苯氧基)丁酸乙酯(CAS号:59227-79-1)?
4-(4-氯苯氧基)丁酸乙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。避免阳光直射,防止容器破裂导致泄漏。储存时应保持容器密封,避免与空气中的水蒸气接...
4-庚基苯乙酮(CAS号:37593-03-6)安全吗?
4-庚基苯乙酮相对安全,但在使用和储存时仍需注意。应避免吸入其蒸气,避免皮肤接触,使用时需佩戴防护眼镜和手套。储存时应远离火源和热源,保持容器密封,放置于阴凉、...
什么是乙基2-氨基-4-(3-溴苯基)噻吩-3-羧酸乙酯(CAS号:438218-48-5)?
乙基2-氨基-4-(3-溴苯基)噻吩-3-羧酸乙酯是一种有机化合物,分子式为C16H12BrN2O2S。它是一种含有噻吩环、氨基、溴苯基和羧酸酯结构的化合物。这...
什么是(9ci)-2-氨基-6-甲基-苯甲酰胺(CAS号:1885-31-0)?
(9ci)-2-氨基-6-甲基-苯甲酰胺是一种化学化合物,其英文名称为2-Amino-6-methylbenzamide,CAS号为1885-31-0。该化合物...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.











![10-(1-Azabicyclo[2.2.2]oct-3-ylmethyl)-10H-phenothiazine structure 10-(1-Azabicyclo[2.2.2]oct-3-ylmethyl)-10H-phenothiazine structure](https://cnstatic.chemtradehub.com/structs/292/29216-28-2-1d81.webp)


