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Journal articles on the topic 'Dimeric Surfactants'

Author: Grafiati

Published: 6 September 2023

Last updated: 31 July 2025

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1

Zana, Raoul. "Gemini (dimeric) surfactants." Current Opinion in Colloid & Interface Science 1, no. 5 (1996): 566–71. http://dx.doi.org/10.1016/s1359-0294(96)80093-8.

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2

Sekhon, B. S. "Gemini (dimeric) surfactants." Resonance 9, no. 3 (2004): 42–49. http://dx.doi.org/10.1007/bf02834987.

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3

Naik, Bharti, Susmita S. Paranjpe, and Chandu S. Madankar. "Cationic Gemini surfactants: a review on synthesis and their applications." Tenside Surfactants Detergents 61, no. 5 (2024): 491–504. http://dx.doi.org/10.1515/tsd-2024-2585.

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Abstract The molecules of Gemini surfactants are dimeric and consist of two monomeric surfactant units linked by a spacer. Among them, cationic Gemini surfactants have a wide range of application in various industrial sectors such as pharmaceuticals, home and personal care, corrosion inhibition, etc. Various methods of synthesis have been investigated and tested for the synthesis of cationic Gemini surfactants. The surface properties of Gemini surfactants are highly dependent on various factors like spacer, headgroups, counterions, etc. The cationic Gemini surfactants have lower CMC values as

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4

Behjatmanesh-Ardakani, Reza, and Maryam Farsad. "On the Difference between Self-Assembling Process of Monomeric and Dimeric Surfactants with the Same Head to Tail Ratio: A Lattice Monte Carlo Simulation." Journal of Chemistry 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/525948.

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Experimental data show that gemini surfactants have critical micelle concentrations that are almost tenfold lower than the CMCs of single chain ones. It is believed that the spacer groups play an important role in this subject. Short hydrophilic or long hydrophobic spacers can reduce CMC dramatically. In this paper, self-assembling processes of double-chain and one-chain surfactants with the same head to tail ratio are compared. Dimeric chain structure is exactly double of single chain. In other words, hydrophilic-lyophilic balances of two chain models are the same. Two single chains are conne

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5

Zana, R., H. Lévy, and K. Kwetkat. "Mixed Micellization of Dimeric (Gemini) Surfactants and Conventional Surfactants. I. Mixtures of an Anionic Dimeric Surfactant and of the Nonionic Surfactants C12E5and C12E8." Journal of Colloid and Interface Science 197, no. 2 (1998): 370–76. http://dx.doi.org/10.1006/jcis.1997.5248.

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6

Tashiro, Katsumi, Keisuke Ohta, Xiaoguang Cui, et al. "Effects of various forms of surfactant protein C on tidal volume in ventilated immature newborn rabbits." Journal of Applied Physiology 94, no. 4 (2003): 1519–26. http://dx.doi.org/10.1152/japplphysiol.00059.2001.

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Surfactant protein (SP)-C is characterized by α-helix structure and palmitoyl groups attached to two cysteine residues. We examined the function of palmitoylation and dimerization in promotion of tidal volume in immature newborn rabbits. Reconstituted surfactants were made from a mixture of synthetic phospholipids and porcine SP-B (basic mixture) by adding various forms of SP-Cs: normal SP-C isolated from porcine lungs and monomeric or dimeric forms of SP-C. These latter two were isolated from patients with pulmonary alveolar proteinosis and were less palmitoylated. Animals were ventilated at

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7

Kumar, Naveen, Rashmi Tyagi, and V. K. Tyagi. "Efficiency of single and mixed dimeric surfactants micelles on solubil-ization of polycyclic aromatic hydrocarbons." Applied Chemical Engineering 3, no. 1 (2020): 8. http://dx.doi.org/10.24294/ace.v3i1.545.

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The solubilization of polycyclic aromatic hydrocarbons (PAHs) such as naphthalene, phenanthrene and pyrene by single and mixed anionic dimeric surfactants was investigated and correlated with micellar properties of these surfactants. The surface and micellar properties of single and binary mixed combinations of anionic dimeric surfactants have been studied through surface tension as well as conductivity measurements at 300 K. The associations between their micelle properties and solubilizing efficiency towards PAHs have been quantified and discussed in terms of the molar solubilization ratio (

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8

Silin, M. A., L. A. Magadova, D. N. Malkin,, P. K. Krisanova, S. A. Borodin, and A. A. Filatov. "Complex Study of a Hydraulic Fracturing Fluid Based on a Pseudo-Dimeric Surfactant." Chemistry and Technology of Fuels and Oils 632, no. 4 (2022): 43–49. http://dx.doi.org/10.32935/0023-1169-2022-632-4-43-49.

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The paper presents a complex study of compositions based on pseudo-dimeric surfactants. Rheological and oscillation studies, proppant test (proppant drop rate and static proppant settling), composition’s influence on clay swelling were carried out.In the course of research, it was found that hydraulic fracturing fluids based on pseudo-dimeric surfactants have advantages over similar systems.

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9

Alargova, R. G., I. I. Kochijashky, M. L. Sierra, K. Kwetkat, and R. Zana. "Mixed Micellization of Dimeric (Gemini) Surfactants and Conventional Surfactants." Journal of Colloid and Interface Science 235, no. 1 (2001): 119–29. http://dx.doi.org/10.1006/jcis.2000.7311.

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10

Castro, Mariano J. L., José Kovensky, and Alicia Fernández Cirelli. "New dimeric surfactants from alkyl glucosides." Tetrahedron 55, no. 44 (1999): 12711–22. http://dx.doi.org/10.1016/s0040-4020(99)00786-3.

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11

Laschewsky, Andr�, Klaus Lunkenheimer, Rivo H. Rakotoaly, and Laurent Wattebled. "Spacer effects in dimeric cationic surfactants." Colloid and Polymer Science 283, no. 5 (2004): 469–79. http://dx.doi.org/10.1007/s00396-004-1219-8.

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12

Datir, Kirti, Harshada Shinde, and Amit P. Pratap. "Preparation of a Gemini Surfactant from Mixed Fatty Acid and its Use in Cosmetics." Tenside Surfactants Detergents 58, no. 1 (2021): 67–73. http://dx.doi.org/10.1515/tsd-2020-2278.

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Abstract Among the surfactants, dimeric surfactants represent a niche group with multifunctional properties. In this work a modified gemini surfactant was synthesized using symmetrical fatty acids. Due to the spacers used to combine the two symmetrical monomers, the synthesized gemini surfactant is cationic. The structure of the compound was confirmed with 1H-NMR. The most advantageous property of the gemini surfactant is that it has a lower surface tension, i. e. less than 35 mNm–1 at 25°C, compared to monomeric surfactants. The surface tension was determined with a Kyowa tensiometer. The CMC

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13

Panda, Manorama, Nazish Fatma, and Mohammad Kamil. "Synthesis, Characterization and Solution Properties of Novel Cationic Ester-Based Gemini Surfactants." Zeitschrift für Physikalische Chemie 233, no. 5 (2019): 707–20. http://dx.doi.org/10.1515/zpch-2017-1000.

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Abstract The present investigation involves the synthesis of a series of novel green ethylene oxide-linked diester-functionalized cationic gemini surfactants 2,2′-[(oxybis(ethane-1,2-diyl))bis(oxy)]bis(N-alkyl-N,N-dimethyl-2-oxoethanaminium) dichloride (Cm-DEG-Cm; m = 12, 14, 16). These compounds were characterized by 1H-NMR, MS-ESI (+), FT-IR spectroscopy and elemental analysis; their solution properties were evaluated by surface tension and rheology measurements. The dimeric surfactant, Cm-DEG-Cm, possesses improved physicochemical properties as compared to its monomeric counterpart. Much lo

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14

Zhao, Jing, Sherril D. Christian, and B. M. Fung. "Mixtures of Monomeric and Dimeric Cationic Surfactants." Journal of Physical Chemistry B 102, no. 39 (1998): 7613–18. http://dx.doi.org/10.1021/jp982131g.

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15

Balcerzak, Mateusz, Zuzanna Pietralik, Ludwik Domka, Andrzej Skrzypczak, and Maciej Kozak. "Adsorption of dimeric surfactants in lamellar silicates." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 364 (December 2015): 108–15. http://dx.doi.org/10.1016/j.nimb.2015.07.135.

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16

Kumar, Naveen, and Rashmi Tyagi. "Industrial Applications of Dimeric Surfactants: A Review." Journal of Dispersion Science and Technology 35, no. 2 (2014): 205–14. http://dx.doi.org/10.1080/01932691.2013.780243.

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17

Pronkin, P. G., L. A. Shvedova, and A. S. Tatikolov. "Effects of Surfactants on the Aggregation of 6,6'-Disubstituted Thiacarbocyanine Dyes in Aqueous Solutions." Химическая физика 43, no. 3 (2024): 3–13. http://dx.doi.org/10.31857/s0207401x24030016.

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The aggregation properties of a number of 6,6'-substituted thiacarbocyanine dyes were studied by spectral-fluorescent methods: T-304, T-306, T-307, T-336 and, for comparison, thiacarbocyanine Cyan 2, which has no substituents in the 6,6'-positions, in aqueous buffer solutions and in the presence of various types of surfactants. The method of moments was used to characterize the absorption spectra (band positions, width, shape). Substituents in the 6,6'-positions significantly increase the ability of dyes T-304, T-306, T-307, T-336 to aggregation (dimerization, as well as to the formation of di

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18

Kowalczyk, Iwona, Anna Koziróg, Adrianna Szulc, Anna Komasa, and Bogumił Brycki. "Antimicrobial Properties of Monomeric and Dimeric Catanionic Surfactant System." Molecules 30, no. 1 (2025): 164. https://doi.org/10.3390/molecules30010164.

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Cationic gemini surfactants are used due to their broad spectrum of activity, especially surface, anticorrosive and antimicrobial properties. Mixtures of cationic and anionic surfactants are also increasingly described. In order to investigate the effect of anionic additive on antimicrobial activity, experimental studies were carried out to obtain MIC (minimal inhibitory concentration) against E. coli and S. aureus bacteria. Two gemini surfactants (12-6-12 and 12-O-12) and two single quaternary ammonium salts (DTAB and DDAC) were analyzed. The most commonly used commercial compounds of this cl

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19

Da Silveira Júnior, Pedro Belchior, Vera Aparecida de Oliveira Tiera, and Marcio José Tiera. "A fluorescence probe study of gemini surfactants in aqueous solution: a comparison between n-2-n and n-6-n series of the alkanediyl-a,w-bis (dimethylalkylammonium bromides)." Ecletica Quimica 32, no. 2 (2007): 47–54. http://dx.doi.org/10.26850/1678-4618eqj.v32.2.2007.p47-54.

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Two series of alkanediyl-a,w-bis (dimethylalkylammonium bromide (n-2-n and n-6-n; n=8, 10,12,and 16) have been synthesized and their micelles properties studied in aqueous solution using pyrene,pyrenecarboxaldehyde (PCA) and 1,8 anilinonaphtalene sulfonic acid sodium salt (ANS) as fluorescentprobes. The micelles from these surfactants have been characterized on the basis of the informationprovided by micelle-solubilized fluorescent probes. The obtained results indicated that the surfactantconcentration at which a marked decrease in l max parameter of pyrenecarboxaldehyde (PCA) occurscorrespond

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20

Naqvi, Andleeb Z., Sahar Noori, and Kabir-ud-Din Kabir-ud-Din. "Mixed micellization of dimeric surfactant–amphiphilic drug systems: effect of surfactant structure." RSC Advances 6, no. 24 (2016): 20324–36. http://dx.doi.org/10.1039/c5ra24058a.

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For their applications as drug delivery vehicles, the mixed interfacial/micellar behaviour of zwitterionic, cocogem and anionic dimeric surfactants with an amphiphilic drug imipramine hydrochloride in aqueous solutions has been investigated.

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21

Turovskaya, M. K., T. M. Prokopyeva, T. S. Gaidash та V. A. Mikhailov. "α-nucleophiles as the basis of organized supernucleophilic microheterogeneous systems for the destruction of rganophosphorus compounds". Vestnik NovSU, № 3 (2023): 374–82. http://dx.doi.org/10.34680/2076-8052.2023.3(132).374-382.

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Peroxyhydrolysis of 4-nitrophenyl esters of phosphoric and phosphonic acids has been studied in organized microheterogeneous systems based on dimeric cationic imidazole-containing surfactants (AlkIm+-(CH2)m-Im+Alk ∙ 2Br- , m = 2,3,4, Alk = C12H25, C14H29). Micellar effects of the surfactants (at pH = const and [surfactant]0 = const) reach ~ 10–100 times. Physicochemical parameters of the peroxyhydrolysis process (such as substrate binding constants, hydroperoxide anion nucleophilicity in micellar pseudophase) are described in terms of the pseudophase distribution model. Observed rate enhanceme

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22

Kumar, Naveen, and Rashmi Tyagi. "Dimeric Surfactants: Promising Ingredients of Cosmetics and Toiletries." Cosmetics 1, no. 1 (2013): 3–13. http://dx.doi.org/10.3390/cosmetics1010003.

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23

Karaborni, S., K. Esselink, P. A. J. Hilbers, et al. "Simulating the Self-Assembly of Gemini (Dimeric) Surfactants." Science 266, no. 5183 (1994): 254–56. http://dx.doi.org/10.1126/science.266.5183.254.

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24

Castro, Mariano J. L., Jose Kovensky, and Alicia Fernandez Cirelli. "ChemInform Abstract: New Dimeric Surfactants from Alkyl Glucosides." ChemInform 31, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.200005233.

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25

Brycki, Bogumił, Małgorzata Waligórska, and Adrianna Szulc. "The biodegradation of monomeric and dimeric alkylammonium surfactants." Journal of Hazardous Materials 280 (September 2014): 797–815. http://dx.doi.org/10.1016/j.jhazmat.2014.08.021.

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26

Shumeiko, Alexander, Michael Kostrikin, Ilya Kapitanov, Anna Serdyuk, Nikolay Burakov, and Anatoly Popov. "Synthesis of functionalized by an oxime group surfactants on the basis of imidazole, pyridine and alkylamines." Ukrainian Chemistry Journal 85, no. 8 (2019): 94–105. http://dx.doi.org/10.33609/0041-6045.85.8.2019.94-105.

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Methods have been developed for the synthe-sis of a series of monomeric and dimeric surfactants functionalized by an oxime group based on imid-azole, pyridine and alkylamines. Alkyl radicals of varying degrees of branching were used, both as sub-stituents at the nitrogen atom of the head group and as spacers in the formation of dimeric products. This allowed to create a whole spectrum of supramo-lecular systems with different physicochemical pro-perties and reactivity.Methods of obtaining a number of intermedi-ate products were improved, primarily for the reac-tion of the imidazole alkylation

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27

Cappelletti, Giuseppe, Silvia Ardizzone, Francesca Spadavecchia, Daniela Meroni, and Iolanda Biraghi. "Mesoporous Titania Nanocrystals by Hydrothermal Template Growth." Journal of Nanomaterials 2011 (2011): 1–9. http://dx.doi.org/10.1155/2011/597954.

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Mesoporous TiO2nanocrystals have been synthetized by a classical sol-gel route integrated by an hydrothermal growth step using monomeric (dodecylpyridinium chloride, DPC) or dimeric gemini-like (GS3) surfactants as template directing agents. Adsorption isotherms at the solid/liquid interface of the two surfactants have been obtained on aqueous dispersion of titania; the nature of the oxide/adsorbate interactions and the molecules orientation/coarea are discussed. The effects produced by the presence of the two surfactants on the different morphological (surface area, porosity, and shape) and s

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28

Andrzejewska, W., M. Wilkowska, M. Chrabąszczewska, and M. Kozak. "The study of complexation between dicationic surfactants and the DNA duplex using structural and spectroscopic methods." RSC Advances 7, no. 42 (2017): 26006–18. http://dx.doi.org/10.1039/c6ra24978g.

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Dicationic (also known as gemini or dimeric) bis-alkylimidazolium surfactants belong to a group of non-viral transfection systems proposed for the successful introduction of different types of nucleic acids (i.e., siRNA, DNA oligomers, and plasmid DNA) into living cells.

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29

Kumar, Naveen, and Rashmi Tyagi. "Characteristic and Application of Anionic Dimeric Surfactants: A Review." Tenside Surfactants Detergents 56, no. 3 (2019): 172–79. http://dx.doi.org/10.3139/113.110614.

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30

Castro, Mariano, José Kovensky, and Alicia Cirelli. "Structure-Properties Relationship of Dimeric Surfactants from Butyl Glucosides." Molecules 5, no. 12 (2000): 608–9. http://dx.doi.org/10.3390/50300608.

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31

Diamant, Haim, and David Andelman. "Dimeric Surfactants: A Simplified Model for the Spacer Chain." Langmuir 11, no. 9 (1995): 3605–6. http://dx.doi.org/10.1021/la00009a055.

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32

Zana, R., and Y. Talmon. "Dependence of aggregate morphology on structure of dimeric surfactants." Nature 362, no. 6417 (1993): 228–30. http://dx.doi.org/10.1038/362228a0.

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33

Renouf, Philippe, Charles Mioskowski, Luc Lebeau, Dominique Hebrault, and Jean-Roger Desmurs. "Dimeric surfactants: First synthesis of an asymmetrical gemini compound." Tetrahedron Letters 39, no. 11 (1998): 1357–60. http://dx.doi.org/10.1016/s0040-4039(97)10835-8.

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34

Weihs, Daphne, Dganit Danino, Aurora Pinazo-Gassol, Lourdes Perez, Elias I. Franses, and Yeshayahu Talmon. "Self-aggregation in dimeric arginine-based cationic surfactants solutions." Colloids and Surfaces A: Physicochemical and Engineering Aspects 255, no. 1-3 (2005): 73–78. http://dx.doi.org/10.1016/j.colsurfa.2004.11.035.

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35

Danino, Dganit, Yeshayahu Talmon, and Raoul Zana. "Vesicle-to-Micelle Transformation in Systems Containing Dimeric Surfactants." Journal of Colloid and Interface Science 185, no. 1 (1997): 84–93. http://dx.doi.org/10.1006/jcis.1996.4545.

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36

Chen, Zhi, Yujun Feng, Dongliang Zhou, Puxin Zhu, and Dacheng Wu. "Synthesis and monolayer film of a series of new twin-tailed gemini cationic surfactants at the air/water interface." Open Chemistry 6, no. 3 (2008): 477–81. http://dx.doi.org/10.2478/s11532-008-0031-6.

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AbstractA series of new dimeric surfactants, twin-tailed gemini surfactants, 2(12)-s-2(12), were successfully prepared and characterized, and their monolayer films investigated by the measurement of surface pressure-area (π-A) and surface pressure-time (π-t) isotherms at the air/water interface by a Langmuir film balance. Compared to their monomeric counterparts, their collapse pressure (γcollapse) is smaller, whilst all the molecular area parameters are larger. The limited area (Alimited) and the initial area (Ainitial) of these twin-tailed gemini surfactants change with increasing spacer len

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37

Azum, Naved, Malik Abdul Rub, Abdullah M. Asiri, Khalid A. Alamry, and Hadi M. Marwani. "Self-Aggregation of Cationic Dimeric and Anionic Monomeric Surfactants with Nonionic Surfactant in Aqueous Medium." Journal of Dispersion Science and Technology 35, no. 3 (2014): 358–63. http://dx.doi.org/10.1080/01932691.2013.788451.

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38

Brunet, Kévin, Cheikh A. B. Diop, Alexia Chauzy, et al. "Improved In Vitro Anti-Mucorales Activity and Cytotoxicity of Amphotericin B with a Pegylated Surfactant." Journal of Fungi 8, no. 2 (2022): 121. http://dx.doi.org/10.3390/jof8020121.

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The aim of this study was to evaluate the effect of the combination of amphotericin B (AmB) and various non-ionic surfactants on the anti-Mucorales activity of AmB, the toxicity of the combination on eukaryotic cells and the modification of AmB aggregation states. Checkerboards were performed on five genera of Mucorales (12 strains) using several combinations of different surfactants and AmB. These data were analyzed by an Emax model. The effect of surfactants on the cytotoxic activity of AmB was then evaluated for red blood cells and two eukaryotic cell lines by absorbance and propidium iodid

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39

Zhao, Jinzhou, Ming Zhou, Xu Wang, and Yan Yang. "Synthesis and Surface Active Properties of Dimeric Gemini Sulfonate Surfactants." Tenside Surfactants Detergents 51, no. 1 (2014): 26–31. http://dx.doi.org/10.3139/113.110282.

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40

Zakharov, Lucia Ya, Vyacheslav E. Semenov, Mikhail A. Voronin, et al. "Supramolecular catalytic systems based on dimeric pyrimidinic surfactants and polyethyleneimine." Mendeleev Communications 18, no. 3 (2008): 158–60. http://dx.doi.org/10.1016/j.mencom.2008.05.016.

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41

Gao, Chunli, Anna Millqvist-Fureby, Michael J. Whitcombe, and Evgeny N. Vulfson. "Regioselective synthesis of dimeric (gemini) and trimeric sugar-based surfactants." Journal of Surfactants and Detergents 2, no. 3 (1999): 293–302. http://dx.doi.org/10.1007/s11743-999-0080-9.

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42

Wang, Wenjing, Dong An, and Zhiwen Ye. "Synthesis and properties of amino acid glucose ester dimeric surfactants." Journal of Dispersion Science and Technology 39, no. 2 (2017): 292–97. http://dx.doi.org/10.1080/01932691.2017.1316204.

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43

Faustino, Célia M. C., António R. T. Calado, and Luís Garcia-Rio. "Dimeric and monomeric surfactants derived from sulfur-containing amino acids." Journal of Colloid and Interface Science 351, no. 2 (2010): 472–77. http://dx.doi.org/10.1016/j.jcis.2010.08.007.

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44

Sharma, K. Shivaji, P. A. Hassan, and Animesh K. Rakshit. "Self aggregation of binary surfactant mixtures of a cationic dimeric (gemini) surfactant with nonionic surfactants in aqueous medium." Colloids and Surfaces A: Physicochemical and Engineering Aspects 289, no. 1-3 (2006): 17–24. http://dx.doi.org/10.1016/j.colsurfa.2006.04.004.

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45

Danino, D., Y. Talmon, and R. Zana. "Alkanediyl-.alpha.,.omega.-Bis(Dimethylalkylammonium Bromide) Surfactants (Dimeric Surfactants). 5. Aggregation and Microstructure in Aqueous Solutions." Langmuir 11, no. 5 (1995): 1448–56. http://dx.doi.org/10.1021/la00005a008.

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46

CHAILLEY-HEU, Bernadette, Sandrine RUBIO, Jean-Philippe ROUGIER, et al. "Expression of hydrophilic surfactant proteins by mesentery cells in rat and man." Biochemical Journal 328, no. 1 (1997): 251–56. http://dx.doi.org/10.1042/bj3280251.

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Human peritoneal dialysis effluent (PDE) contains a phosphatidylcholine-rich compound similar to the surfactant that lines lung alveoli. This material is secreted by mesothelial cells. Lung surfactant is also characterized by four proteins essential to its function. After having long been considered as lung-specific, some of them have been found in gastric and intestinal epithelial cells. To explore further the similarity between lung and peritoneal surfactants, we investigated whether mesothelial cells also produce surfactant proteins. We used rat transparent mesentery, human visceral periton

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47

Andrzejewska, Weronika, Michalina Wilkowska, Andrzej Skrzypczak, and Maciej Kozak. "Ammonium Gemini Surfactants Form Complexes with Model Oligomers of siRNA and dsDNA." International Journal of Molecular Sciences 20, no. 22 (2019): 5546. http://dx.doi.org/10.3390/ijms20225546.

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Dimeric cationic surfactants (gemini-type) are a group of amphiphilic compounds with potential use in gene therapy as effective carriers for nucleic acid transfection (i.e., siRNA, DNA, and plasmid DNA). Our studies have shown the formation of lipoplexes composed of alkanediyl-α,ω-bis[(oxymethyl)dimethyldodecylammonium] chlorides and selected 21-base-pair nucleic acid (dsDNA and siRNA) oligomers. To examine the structure and physicochemical properties of these systems, optical microscopy, circular dichroism spectroscopy (CD), small-angle X-ray scattering of synchrotron radiation (SR-SAXS), and

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48

Selmani, Atiđa, Johannes Lützenkirchen, Kristina Kučanda, et al. "Tailoring the stability/aggregation of one-dimensional TiO2(B)/titanate nanowires using surfactants." Beilstein Journal of Nanotechnology 10 (May 13, 2019): 1024–37. http://dx.doi.org/10.3762/bjnano.10.103.

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The increased utilization of one-dimensional (1D) TiO2 and titanate nanowires (TNWs) in various applications was the motivation behind studying their stability in this work, given that stability greatly influences both the success of the application and the environmental impact. Due to their high abundance in aqueous environments and their rich technological applicability, surfactants are among the most interesting compounds used for tailoring the stability. The aim of this paper is to determine the influence of surfactant molecular structure on TNW stability/aggregation behavior in water and

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49

Aswal, V. K., S. De, P. S. Goyal, S. Bhattacharya, and R. K. Heenan. "Small-angle neutron scattering study of micellar structures of dimeric surfactants." Physical Review E 57, no. 1 (1998): 776–83. http://dx.doi.org/10.1103/physreve.57.776.

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Jurašin, Darija, Igor Weber, and Nada Filipović-Vinceković. "Phase Behavior in Mixtures of Cationic Dimeric and Anionic Monomeric Surfactants." Journal of Dispersion Science and Technology 30, no. 5 (2009): 622–33. http://dx.doi.org/10.1080/01932690802598481.

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