1982
DOI: 10.1002/pol.1982.170200625
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Nonionic polymer surfactants

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Cited by 8 publications
(8 citation statements)
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“…This behavior does not indicate a classical overlap but the presence of a rheologically significant network across the system. This phenomenon has been reported in carboxymethyl cellulose (Charpentier-Valenza et al 2005), carboxymethyl pullulans (Simon et al 2003) and hmHEC (Maestro et al 2002a;Landoll 1982). As explained in the theory section, these studies suggest that the aggregates of more than one polymer chain exist even at very low concentrations of amphiphilic polymers.…”
Section: Calculation Of Intrinsic Viscositysupporting
confidence: 71%
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“…This behavior does not indicate a classical overlap but the presence of a rheologically significant network across the system. This phenomenon has been reported in carboxymethyl cellulose (Charpentier-Valenza et al 2005), carboxymethyl pullulans (Simon et al 2003) and hmHEC (Maestro et al 2002a;Landoll 1982). As explained in the theory section, these studies suggest that the aggregates of more than one polymer chain exist even at very low concentrations of amphiphilic polymers.…”
Section: Calculation Of Intrinsic Viscositysupporting
confidence: 71%
“…Hydrophobically modified hydroxyethyl cellulose (hmHEC) has been studied extensively over last few decades after its first academic investigation published by Landoll 1982(Maestro et al 2002bChassenieux et al 2010;Zhang 2001;Laschet et al 2004;Zhao and Chen 2007;Gonzalez et al 2005;Patruyo et al 2002). This polymer is synthesized by grafting hydrophobic 'sticker' groups across the hydrophilic backbone of HEC.…”
Section: Introductionmentioning
confidence: 99%
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“…In the recent years, the cellulose based on material functional has been receiving increasing attention as it does [4][5][6][7][8][9][10][11][12][13][14][15] . The amphiphilic cellulose derivatives, which were synthesized through the reaction of nonionic cellulose ethers like hydroxyethyl cellulose (HEC), hydroxypropyl cellulose (HPC) and methylcellulose (MC) with long-chain n-alkyl epoxides, was first studied at 1982 by Landoll [16] . Science then, a large part of the work about the cellulose derivatives bearing various hydrophobic residues, such as alkyl groups, bulky phenoxyhydroxypropyl groups, poly (e-caprolactone) segments, and poly(methyl methacrylate) segment, have been successfully synthesized [17][18][19][20][21][22][23][24][25] .…”
Section: Introductionmentioning
confidence: 99%
“…The hydrophobes associate with one another in aqueous solutions at low concentrations, and thereby increase the viscosity of the solution at low shear frequencies [21]. Examples of commercial associative thickeners include hydrophobically modified HEC (HMHEC) [22], ethoxylated urethane (HEUR) [23,24], and alkali-soluble emulsion (HASE) [25][26][27]. Enzyme catalysis can be used to put a hydrophobic unit onto a cellulose derivative.…”
Section: Addition Of Hydrophobic Substituentsmentioning
confidence: 99%