Synergism in Mixed Anionic–Amphoteric Surfactant Solutions: Influence of Anionic Surfactant Chain Length

2009 ◽  
Vol 46 (5) ◽  
pp. 298-305 ◽  
Author(s):  
R. Abdel-Rahem
Langmuir ◽  
2005 ◽  
Vol 21 (17) ◽  
pp. 7662-7671 ◽  
Author(s):  
Emil Chibowski ◽  
Agnieszka Wiacek ◽  
Lucyna Holysz ◽  
Konrad Terpilowski

Author(s):  
Kenjiro Meguro ◽  
Hiroyuki Akasu ◽  
Minoru Ueno ◽  
Tomoo Satake

Weed Science ◽  
1976 ◽  
Vol 24 (6) ◽  
pp. 549-552 ◽  
Author(s):  
J. D. Gaynor ◽  
V. V. Volk

The effects of soil organic matter, clay, extractable Al, cation exchange capacity, and pH on the adsorption of picloram (4-amino-3,5,6-trichloropicolinic acid) from aqueous and surfactant solutions were investigated. Linear adsorption isotherms for the soils were obtained with the Freundlich equation. Of the five soil properties investigated, Freundlich K values correlated with extractable Al and clay content. Picloram adsorption from aqueous solutions and from the non-ionic and anionic surfactant solutions was greater on the soils at pH 5 than at pH 7. The anionic surfactant competed with picloram for adsorption sites on the soils at pH 5. Picloram adsorption from solutions containing 0.1 and 1% cationic surfactant was greater than that from aqeuous and anionic and nonionic surfactant solutions. Picloram adsorption from the 10% cationic surfactant solution was similar on soils with pH 5 and 7 and increased with decreased organic matter content.


2015 ◽  
Vol 19 (07) ◽  
pp. 845-851 ◽  
Author(s):  
Margaret A. Gradova ◽  
Vladimir V. Artemov ◽  
Anton V. Lobanov

Porphyrin-surfactant interactions in aqueous solutions are known to result in the selfassembly of various supramolecular structures, including pigment-surfactant complexes, J- and H-aggregates, and solubilized dye species. Detailed studies on the mechanisms of the intermolecular interactions governing the above self-assembly processes allow to predict the aggregation state and hence, the photophysical properties of the dye-surfactant assemblies in order to perform a direct synthesis of the desired porphyrin-based nanostructures at the appropriate experimental conditions. This paper describes a novel example of the surfactant-induced J-aggregate formation from the diprotonated hydrophobic tetraphenylporphyrin species in submicellar aqueous anionic surfactant solutions. The above assemblies are characterized by a rod-like morphology and possess supramolecular chirality according to the CD measurements.


Langmuir ◽  
2001 ◽  
Vol 17 (23) ◽  
pp. 7219-7224 ◽  
Author(s):  
Kei Watanabe ◽  
Yasunari Nakama ◽  
Toshio Yanaki ◽  
Heinz Hoffmann

2020 ◽  
Vol 4 (3) ◽  
pp. 34
Author(s):  
Pengxiang Li ◽  
Tiejian Li ◽  
Munehide Ishiguro ◽  
Yang Su

Adsorption of a cationic surfactant dodecyl pyridinium chloride (DPC) on silica was studied to show a comparison with the adsorption of an anionic surfactant sodium dodecyl sulfate (SDS), whose carbon chain length is the same and on the same silica. Results provided a better understanding of the adsorption mechanism of cationic and anionic surfactant on negatively charged silica. The experiment covered different electrolyte concentrations and pH values. Results indicated that at the same pH, the DPC adsorption amounts are higher when the electrolyte concentration is higher; at a higher DPC equilibrium concentration, the adsorption amount difference is larger than that at low DPC equilibrium concentration, and when DPC equilibrium concentration is lower than 0.1 mmol/L, the adsorption amount difference cannot be observed. At charge compensation point (CCP, 0 zeta potential), the negative surface charge of silica was compensated by DP+, a continuous increasing zeta potential indicated a bilayer adsorption of DPC on silica. The adsorption amount increased with increasing pH. The calculated lines by Gu and Zhu model show a two-step property, including a bilayer and hemi-micelle adsorption. DPC adsorbed more strongly on silica than SDS due to the combination of electrostatic and hydrophobic attraction.


Langmuir ◽  
2011 ◽  
Vol 27 (16) ◽  
pp. 9815-9822 ◽  
Author(s):  
Ting Lu ◽  
Lian’gen Xia ◽  
Xiaodong Wang ◽  
Aiqing Wang ◽  
Tao Zhang

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