2011
DOI: 10.1039/c0sm00885k
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Molecular interactions of polymer oleogelation

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Cited by 171 publications
(128 citation statements)
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“…Polymerpolymer interactions occur within OH groups of different molecules or of one chain to another, involving only hydrogen bond interactions and no direct electrostatic interaction with the oil (Laredo et al, 2011). In this case, the main changes observed in the IR spectra are due to polymer-polymer interaction by hydrogen bounding to form an oleogel structure (above 3000 cm −1…”
Section: Fourier Transform Infrared Spectroscopymentioning
confidence: 99%
See 1 more Smart Citation
“…Polymerpolymer interactions occur within OH groups of different molecules or of one chain to another, involving only hydrogen bond interactions and no direct electrostatic interaction with the oil (Laredo et al, 2011). In this case, the main changes observed in the IR spectra are due to polymer-polymer interaction by hydrogen bounding to form an oleogel structure (above 3000 cm −1…”
Section: Fourier Transform Infrared Spectroscopymentioning
confidence: 99%
“…The band at approximately 3300 cm −1 corresponds to hydrogen bonding between the un-substituted OH groups of the cellulose backbone (Laredo et al, 2011) (Figure 5).…”
Section: Fourier Transform Infrared Spectroscopymentioning
confidence: 99%
“…Initially, poly(O-benzyl-l-serine) 20 was synthesised by the ROP of O-benzyl-l-serine NCA, using benzylamine as the initiator, before the benzyl ether protecting group was cleaved from the polymer to yield PS (Scheme 1), as confirmed by 1 H NMR spectroscopy (Fig. S2, ESI ) and FTIR (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Examples of vegetable oil-based organogels include organic gelators dispersed within sunflower oil, 18 safflower oil 19 and linseed oil. 20 Barbut and co-workers demonstrated an ethylcellulose-canola oil organogel as a potential replacement for the animal fat in frankfurters. 21 Marangoni and co-workers also demonstrated the use of canola oil as the solvent in 12-hydroxystearic acid-containing organogels that displayed tuneable crystallinity and oil binding capacity, depending on their storage temperature.…”
Section: Introductionmentioning
confidence: 99%
“…In most cases, low-molecular weight amphiphilic molecules which impart thermo-reversible properties are responsible for the gelling behaviour [13][14][15][16][17]. However, some biomacromolecules like natural waxes, resins and biopolymers with gelling properties in oily media are gaining special attention [18][19][20][21][22][23][24][25][26]. Among these studies, lignocellulosic materials and cellulose derivatives have been used to obtain gel-like dispersions in vegetable oils, which may be potentially applied as environmentally friendly lubricating grease formulations [27][28][29][30][31][32].…”
Section: Introductionmentioning
confidence: 99%