Surface Chemical Properties and Micellization of Disodium Hexadecyl Diphenyl Ether Disulfonate in Aqueous Solution

The surface tension of disodium hexadecyl diphenyl ether disulfonate (C₁₆‐MADS) was measured at different NaCl concentrations (0.00–0.50 mol L^?1) and temperatures (298.0–318.0 K) using the drop‐volume method. The results show that, with increasing temperature, the critical micelle concentration (CMC) of C₁₆‐MADS increases slightly, but the maximum surface adsorption capacity (Γ_max) at the air–water interface decreases. When the concentration of NaCl was increased from 0.00 to 0.50 mol L^?1, the CMC of C₁₆‐MADS decreased from 1.45 × 10^?4 to 4.10 × 10^?5 mol L^?1, but the surface tension at the CMC (γ_cmc) was not affected. When the concentration of NaCl was increased at 298.0 and 303.0 K, the Γ_max of C₁₆‐MADS increased. When the temperature was increased from 308.0 to 318.0 K, the surface excess concentration (Γ_max) of C₁₆‐MADS abnormally decreased from 2.26 to 1.41 μmol m^?2 with increasing NaCl concentration. The micellization free energy () decreased from ?63.98 to ?76.20 kJ mol^?1 with increase of temperature and NaCl concentration. The micellar aggregation number (N_m) of disodium hexadecyl diphenyl ether disulfonate (C₁₆‐MADS) was determined using the molecule fluorescence probe method with pyrene as probe and benzophenone as quencher. The results show that an appropriate N_m could be measured only at surfactant concentration above the CMC. The N_m increased with an increase in C₁₆‐MADS concentration, but the micropolarity in the micelle nucleus decreased. The temperature had little effect on N_m. Compared with typical single hydrophilic headgroup surfactants, aggregates of C₁₆‐MADS exhibit different properties.     

Synthesis and Properties of a Novel Linear Alkylated Diphenylmethane Sulfonate Gemini Surfactant

The linear alkylated diphenylmethane sulfonate (C₁₂‐DSDM) was synthesized by a four‐step reaction with lauric acid, diphenylmethane and chlorosulfonic acid as raw materials. The structure of the final product was characterized by MS. The air–liquid surface tensions at various temperatures and salt solutions (NaCl) were measured by using the drop‐volume technique and the thermodynamic parameters of the micellization were calculated. The results show that the critical micelle concentration (CMC) and γ_CMC of the surfactant are 1.452 mmol L^?1 and 38.49 mN m^?1 at 298 K. With an increase in temperature, the CMC gradually increases, the γ_CMC and the maximum surface adsorption capacity Γ_max decrease. The free energy of micelle formation is negative (?51.2 to ?60.5 kJ mol^?1).     

Synthesis and Properties of Novel Phenylenediamine Gemini Surfactants

In the present work, a two-step method was adopted to synthesize a series of novel Gemini surfactants using N,N-dimethylalkyl amines (alkyl length = C₁₂, C₁₆ and C₁₈), epichlorohydrin, and n-phenyllenediamine as starting materials. The products were characterized using mass spectroscopy (MS) and nuclear magnetic resonance spectroscopy (¹H NMR). Systematic experiments were conducted to evaluate their surface activity, foaming properties, and antibacterial performance. Results showed the critical micelle concentrations (CMC) of the C₁₂-based, C₁₆-based, and C₁₈-based phenylenediamine surfactants were 3.295 × 10⁻³, 2.532 × 10⁻⁴, and 3.140 × 10⁻⁴ mol L⁻¹ at 298 K, respectively, with corresponding surface tension (γ_cmc) values of 28.24, 31.95, and 35.06 mN m⁻¹ under the same conditions. The Gemini surfactants showed not only good surface activity and foaming properties, but also demonstrated good antimicrobial performance against Gram-positive and Gram-negative bacteria and fungi.     

Sulfated Zirconium Catalyst for Synthesis of Dialkylated Diphenylether Disulfonate Gemini Surfactants

Dialkylated diphenylether disulfonate with different alkyl chain lengths (C_n‐DADS, n = 8, 10 and 12) has been synthesized by Friedel‐Crafts alkylation of olefins (C₈, C₁₀ and C₁₂) and diphenyl oxide, followed by sulfonation and neutralization with fuming sulfuric acid. Sulfated zirconia solid acids were prepared and used to catalyze the alkylation reaction. The structure of sulfated zirconia solid acids was identified by infrared spectroscopy. The title compounds were confirmed by infrared spectroscopy and electrospray ionization‐mass spectrometry. Equilibrium surface tension measurements show that the critical micelle concentration (CMC) decreases with an increase in chain length, and the surface tension at CMC (γ_cmc) of C₈‐DADS is the lowest. The minimum area per molecule (A_min) values of C_n‐DADS increase, while the surface excess concentration (Γ_max) values decrease with the increase of the alkyl chain length. C₁₀‐DADS has the highest pC₂₀ and CMC/C₂₀ among C_n‐DADS.     

Synthesis and Performance Evaluation of CO2/N2 Switchable Tertiary Amine Gemini Surfactant

A type of switchable tertiary amine Gemini surfactant, N,N′‐di(N,N‐dimethyl propylamine)‐N,N′‐didodecyl ethylenediamine, was synthesized by two substitution reactions with 3‐chloro‐1‐(N,N‐dimethyl) propylamine, bromododecane and ethylene diamine as main raw materials. The structure of the product was characterized by FTIR and ¹H‐NMR. We also investigated the surface tension when CO₂ was bubbled in different concentrations of surfactant solution and the influence of different CO₂ volumes on surface tension under a constant surfactant concentration. Finally the surface tension curve and the related parameters were acquired by surface tension measurements. The experimental results showed that the structure of the synthesized compounds were in conformity with the expected structure of the surfactant, and displayed a better surface activity after bubbling CO₂. The critical micelle concentration (CMC) surface tension at CMC (γ_cmc) pC₂₀ (negative logarithm of the surfactant's molar concentration C₂₀, required to reduce the surface tension by 20 mN/m) surface excess (Γ_max) at air/solution interface and the minimum area per surfactant molecule at the air/solution interface (A_min) were determined. Results indicate that the target product had good surface activity after bubbling CO₂.     

Synthesis and Surface Properties of Novel Carboxylic Ester-Containing Imidazolium-Based Zwitterionic Surfactants: Monoalkyl 2-(3-Methylimidazolium-1-yl) Succinate Inner Salts

A series of carboxylic ester‐containing imidazolium‐based zwitterionic surfactants, namely, monoalkyl 2‐(3‐methylimidazolium‐1‐yl) succinate inner salts (C_nMimSU, n = 8, 10, 12 and 14), have been synthesized. Their structures were confirmed by ¹H NMR, ¹³C NMR and FTIR. The typical physicochemical properties parameters such as isoelectric point, critical micelle concentration (CMC), surface tension at CMC (γ_CMC), surface pressure at CMC (Π_CMC), adsorption efficiency (pC₂₀), the maximum surface excess (Γ_m), the minimum molecular cross‐sectional area (A_min) and the value of CMC/C₂₀ were determined. The effect of the long‐chain length on the important physicochemical properties of C_nMimSU was studied. It is found that the surface activity of C_nMimSU is enhanced with the long‐chain length increases.     

Synthesis and Surface Properties of Disodium Monoalkyl Diphenyl Oxide Disulfonate

Disodium monoalkyl diphenyl oxide disulfonates (MADS) with different carbon chains (C_n‐MADS, n = 8, 12, 16) were synthesized through the steps of alkylation‐sulfonation‐neutralization using fatty alcohols (C₈, C₁₂, C₁₆), diphenyl oxide and fuming sulfuric acid (20 % free SO₃) as reagents. The structures of the products were identified by infrared spectroscopy and electrospray ionization‐mass spectrometry. The surface properties, emulsification, wettability alteration and salinity and hardness tolerance of the products were systematically investigated. The results show that the critical micelle concentration (CMC) of C₈MADS, C₁₂MADS and C₁₆MADS are 7.24 × 10^?3, 1.49 × 10^?3 and 2.09 × 10^?4 mol/L. The surface tensions at the CMC (γ_CMC) of each product are 37.5, 38.9 and 46.8 mN/m. The negative logarithm of the surfactant concentration in the bulk phase required to produce a 20 mN/m reduction in the surface tension of the solvent (pC₂₀) increases with the increase in the alkyl chain length. The emulsifying ability of C₁₂‐MADS is better than C₈‐MADS and C₁₆‐MADS, and the MADS showed less oil‐wet nature. The salinity and hardness tolerance of MADS is much stronger than that of conventional surfactants.     

A Novel Bola‐Type Rosin‐Based Functional Surfactant and Its Synergistic Effect with Natural Surfactant Saponin

A novel bola‐type acrylic‐modified rosin ester tertiary ammonium salt surfactant (AETAS) with two hydrophilic groups and a rigid hydrophobic group was synthesized through a simple method from rosin acid, which is a natural raw material. The chemical structure of the synthesized surfactant was confirmed by infrared spectroscopy and nuclear magnetic resonance spectroscopy (¹H NMR and ¹³C NMR). The critical micelle concentration (CMC) of the AETAS was 0.44 g/L, and the surface tension at the CMC (γ_cmc) was 45.02 mN/m. Self‐assembly behavior of the AETAS in aqueous solution was characterized by transmission electron microscopy. The micelle diameter of the AETAS was about 150 nm in aqueous solution. We also explored the synergy of the AETAS and soapnut saponin. The binary surfactant compound systems of the AETAS and soapnut saponin had obvious synergistic effect in enhancing surface activity when the mass ratio of AETAS/soapnut saponin was 1:1. The γ_cmc of soapnut saponin was 47.70 mN/m when the concentration reached 0.46 g/L, but the γ_cmc of mixtures decreased to 44.26 mN/m at 0.30 g/L. The emulsification ability of the mixtures was significantly improved and the emulsion performance increased from 245 to 595 s when the mass ratio of AETAS/soapnut saponin was 1:1.     

Effect of Polar Organic Solvents on Self‐Aggregation of Some Cationic Monomeric and Dimeric Surfactants

Surface and micellization behavior of some cationic monomeric surfactants, viz., cetyldiethylethanolammonium bromide (CDEEAB), cetyldimethylethanolammonium bromide (CDMEAB), tetradecyldiethylethanolammonium bromide (TDEEAB) and dimeric surfactants, i.e., alkanediyl‐α, ω‐bis(dimethylhexadecylammonium bromide) (C₁₆‐s‐C₁₆, 2Br^? where s = 4, 12), butanediyl‐1,4‐bis(dimethyldodecylammonium bromide (C₁₂‐4‐C₁₂, 2Br^?) and 2‐butanol‐1,4‐bis(dimethyldodecylammonium bromide) (C₁₂‐4(OH)‐C₁₂, 2Br^?), was studied in water‐organic solvents [10 and 20 % v/v ethylene glycol (EG) and diethylene glycol (DEG)] by conductivity, surface tension and steady‐state fluorescence methods at 300 K. The main focus of the present work is on the study of the effect of organic solvents on the critical micelle concentration (CMC), Gibbs free energy of micellization (ΔG°_m), Gibbs free energy of transfer (ΔG°_trans), Gibbs adsorption energy (ΔG°_ads) and some interfacial parameters such as the surface excess concentration (Γ_max), minimum area per surfactant molecule (A_min) and surface pressure (π_CMC). The aggregation number (N_agg) and Stern‐Volmer quenching constant (K_SV) were also determined by the steady‐state fluorescence method. It was observed that N_agg decreased with increasing volume percent of organic solvent. The results exhibited an increase in CMC in water‐organic solvents as compared to the respective surfactants in pure water. The negative values of ΔG°_m and ΔG°_ads indicate a spontaneous micellization process. The thermodynamics of micellization revealed that the micellization‐reducing efficiency of glycols increases with the concentration and the number of ethereal oxygens in the glycol.     

Effect of Polyoxyethylene Chain Length on the Physicochemical Properties of N,N‐Dimethyl‐N‐dodecyl Polyoxyethylene Amine Oxide Hybrid Surfactants (C12EOnAO,with n = 1–4)

In order to determine the structure‐performance relationship of nonionic‐zwitterionic hybrid surfactants, N,N‐dimethyl‐N‐dodecyl polyoxyethylene (n) amine oxides (C₁₂EO_nAO) with different polyoxyethylene lengths (EO_n, n = 1–4) were synthesized. For homologous C₁₂EO_nAO, it was observed that the critical micelle concentration (CMC), the maximum surface excess (Γ_m), CMC/C₂₀, and the critical micelle aggregation number (N_m,c) decreased on going from 1 to 4 in EO_n. However, there were concomitant increases in surface tension at the CMC (γ_CMC), minimum molecular cross‐sectional area (A_min), adsorption efficiency (pC₂₀), and the polarity ([I₁/I₃]_m) based on the locus of solubilization for pyrene. The values of log CMC and N_m,c decreased linearly with EO_n lengthening from 1 to 4, although the impact of each EO unit on the CMC of C₁₂EO_nAO (n = 1–4) was much smaller than that typically seen for methylene units in the hydrophobic main chains of traditional surfactants. Compared to the structurally related conventional surfactant N,N‐dimethyl‐N‐dodecyl amine oxide (C₁₂AO), C₁₂EO_nAO (n = 1–4) have smaller CMC, A_min, and CMC/C₂₀, but larger pC₂₀, Γ_m, and N_m,c with a higher [I₁/I₃]_m. This may be attributed to the moderately amphiphilic EO_n (n = 1–4) between the hydrophobic C₁₂ tail and the hydrophilic AO head group.     

Synthesis,Surface and Interfacial Properties of Dodecyl Diphenyl Oxide Disulfonate with Different Counterions

Dodecyl diphenyl oxide disulfonate with different counterions (C₁₂MADS‐M, M = Na, Mg, Ca) were synthesized using dodecyl alcohol, diphenyl oxide and SO₃ as reagents through alkylation–sulfonation–neutralization. The structure of the product was characterized by infrared spectroscopy and electrospray ionization‐mass spectrometry. The surface and interfacial prosperities were investigated. The critical micelle concentration (CMC) of C₁₂MADS‐Na, C₁₂MADS‐Mg and C₁₂MADS‐Ca was 1.23 × 10^?3, 5.25 × 10^?4 and 5.37 × 10^?4 mol/L, respectively. The surface tension at CMC (γ_CMC) of C₁₂MADS‐Na, C₁₂MADS‐Mg and C₁₂MADS‐Ca was 43.2, 37.1 and 36.6 mN/m, respectively. Interfacial tensions between crude oil and C₁₂MADS‐M aqueous solution gave only a small change in the calcium chloride concentrations ranging from 50 to 10,000 mg/L.     

Synthesis, Surface and Thermodynamic Properties of Substituted Polytriethanolamine Nonionic Surfactants

Three series of nonionic surfactants derived from polytriethanolamine containing 8, 10, and 12 units of triethanolamine were synthesized. Structural assignment of the different compounds was made on the basis of FTIR and ¹H‐NMR spectroscopic data. The surface parameters of these surfactants included critical micelle concentration (CMC), surface tension at the CMC (γ_CMC), surfactant concentration required to reduce the surface tension of the solvent by 20 mN m^?1 (pC₂₀), maximum surface excess (Γ_max), and the interfacial area occupied by the surfactant molecules (A_min) using surface tension measurements. The micellization and adsorption free energies were calculated at 25 °C.     

Micellar Properties of Surface Active Ionic Liquid Lauryl Isoquinolinium Bromide and Anionic Polyelectrolyte Poly(Acrylic Acid Sodium Salt) in Aqueous Solution

The complex formation between anionic polyelectrolyte poly(acrylic acid sodium salt) [NaPAA] and surface active ionic liquid (SAIL) lauryl isoquinolinium bromide [C₁₂iQuin][Br] in aqueous media has been investigated by surface tension, isothermal titration calorimetry (ITC), and conductance. The self‐assembled structures have been characterized using dynamic light scattering (DLS) and turbidity measurements. A range of surface parameters have been calculated from tensiometric measurements including critical micelle concentration (CMC), surface excess concentration (Γ_cmc), surface pressure at the interface (Π_cmc), minimum area occupied at air–solvent interface (A_min), adsorption efficiency (pC₂₀), and surface tension at the CMC (γ_cmc). The thermodynamic parameters, i.e., standard enthalpy of micellization , standard free energy of micellization (), and standard entropy of micellization () have also been evaluated. Four different stages of transitions, corresponding to the progressive formation of NaPAA–[C₁₂iQuin][Br] complex (C₁)_, critical aggregation concentration (CAC), critical saturation concentration (C₃) and CMC have been observed owing to strong electrostatic and hydrophobic interactions. The results obtained from DLS and turbidity measurements show that size of the aggregates first decreases and then increases in the presence of polyelectrolyte. The binding isotherms obtained using isothermal titration calorimetry (ITC) show the concentration dependence as well as the highly cooperative nature of interactions corresponding to formation of polyelectrolyte–SAIL complexes.     

Aggregation Behavior of Mixed Micellar System of Dodecyl Sulfate-Based Surface-Active Ionic Liquids and Anionic Surfactant in Aqueous Media

Mixed micellization behavior of dodecyl sulfate-based ionic liquids, i.e., 1-propyl-3-methylimidazolium dodecyl sulfate [C₃mim][DS] and 1-hexyl-3-methylimidazolium dodecyl sulfate [C₆mim][DS] with sodium dodecyl sulfate (SDS), is investigated at (298.15, 308.15, and 318.15) K in aqueous medium. For this, the conductometric measurements are carried out to evaluate the critical micelle concentrations (cmc ), ideal critical micelle concentration (cmc* ), degree of counterion dissociation (g ), thermodynamic parameters, micellar mole fraction of ionic liquids, and interaction parameter (β) of the mixed system based on the different proposed models given in the literature. Further surface tension measurements have been carried out to confirm the value of cmc obtained via a conductivity study for all the studied systems at 298.15 K. Other surface parameters, such as surface tension at cmc (γ_cmc ), surface pressure (ᴨ_cmc ), surface excess (Γ_max ), and minimum area per molecule (A_min), have also been evaluated for both the systems.     

3-Chloro-2-hydroxypropyl Dimethyl Dehydroabietyl Ammonium Chloride: Synthesis,Characterization, and Physicochemical Properties

3‐Chloro‐2‐hydroxypropyl dimethyl dehydroabietyl ammonium chloride (CHPDMDHA) was synthesized from dehydroabietylamine (DHA) and epichlorodrin. The synthesis was done in three steps. First, DHA was transformed into N,N‐dimethyl dehydroabietyl amine (DMDHA) through Eschweiler‐Clarke Reaction. Second, the DMDHA was reacted with hydrochloric acid and translated into DMDHA hydrochloride. Third, the CHPDMDHA was obtained after the DMDHA hydrochloride had reacted with epichlorodrin and recrystallized using a solvent composed of ethyl acetate and ethanol. The critical micelle concentrations (CMC) of CHPDMDHA at 25 °C was found to be 2.56 × 10^?4 mol L^?1, and its surface tension at the CMC (γ_CMC) was determined to be 27.4 mN m^?1; these data suggest that the surface activities of CHPDMDHA are better than those of benzalkonium chloride (BC), so that CHPDMDHA could be used as a good alternative to BC.     

Synthesis,Characterization and Properties of <Emphasis Type="Italic">N</Emphasis>-Alkyl-<Emphasis Type="Italic">N</Emphasis>,<Emphasis Type="Italic">N</Emphasis>-di(2-hydroxyethyl) Amine Oxides

N‐Dodecyl‐N,N‐di(2‐hydroxyethyl) amine oxide (C₁₂DHEAO) and N‐stearyl‐N,N‐di(2‐hydroxyethyl) amine oxide (C₁₈DHEAO) were synthesized with N‐alkyl‐diethanolamine and hydrogen peroxide. Their chemical structures were confirmed using ¹H‐NMR spectra, mass spectral fragmentation and FTIR spectroscopic analysis. It was found that C₁₂DHEAO and C₁₈DHEAO reduced the surface tension of water to a minimum value of approximately 28.75 mN m^?1 at concentration of 2.48 × 10^?3 mol L^?1 and 32.45 mN m^?1 at concentration of 5.21 × 10^?5 mol L^?1, respectively. The minimum interfacial tension (IFT_min) and the dynamic interfacial tension (DIT) of oil–water system were measured. When C₁₈DHEAO concentration was in the range of 0.1–0.5%, the IFT_min between liquid paraffin and C₁₈DHEAO solutions all reached the ultra‐low interfacial tension. Furthermore, their foam properties were investigated by Ross‐Miles method, and the height of foam of C₁₂DHEAO was 183 mm. It was also found that they showed strong emulsifying power.     

Interfacial and Solution Behavior of Amphiphilic Drug and Counterion‐Coupled Gemini (COCOGEM) Surfactants

The critical micelle concentrations (cmc) of mixed systems comprising an amphiphilic drug amitriptyline hydrochloride and counterion‐coupled gemini surfactants 12‐6‐12, 14‐6‐14, or 16‐6‐16 [1,6‐bis(N,N‐alkyldimethylammonium) adipate] were determined using tensiometry. The results were analyzed in the light of different theoretical models from Rosen, Clint, Rubingh, and Motomura. The cmc values decrease with increasing mole fraction of surfactant (α₁). The cmc_id values (cmc value at ideal mixing conditions) also decrease with α₁ but remain above the experimental cmc values. This means that the mixed micelles form as a result of attractive interactions. These interactions are also seen in surface excess concentration (Γ_max) and minimum area per molecule (A_min) data: Γ_max increases and A_min decreases. Both Rosen's and Rubingh's models indicate synergistic interactions (interaction parameter, β^m and β^σ, values are negative). The β^m values are larger in magnitude than β^σ for 14‐6‐14 and 16‐6‐16 systems, whereas the reverse is the case with 12‐6‐12 because the surfactant's short chain makes adjustment in the core difficult for both components.     

Kinetics of the anionic ring‐opening polymerization of octamethylcyclotetrasiloxane initiated by potassium isopropoxide

Kinetics of the anionic ring‐opening polymerization of octamethylcyclotetrasiloxane (D₄) in bulk initiated by potassium isopropoxide was studied. Several promoters including N‐methyl‐2‐pyrrolidinone (NMP), N,N‐dimethylformamide (DMF), and diglyme were used. It is indicated that the reactions are first‐order in D₄ during the initial stage of polymerization. The polymerization rate of D₄ is influenced by a number of factors, such as the nature of promoters, the molar ratio of promoter to initiator (C_p/C_i ratio), and the reaction temperatures. With the use of NMP as promoter, the polymerization rate constant at 30°C is 10.482 h^?1 with the C_p/C_i ratio equal to 3.0. As the C_p/C_i ratio increases, the polymerization rate constant increases sharply and the cyclic oligomers content in polymer decreases evidently. The back‐biting reaction that leads to the formation of decamethylcyclopentasiloxane (D₅) occurred in the polymerization of D₄. The rate of the D₅ formation relatively to the rate of D₄ conversion increases with the conversion of D₄. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3510–3516, 2006     

Interaction Between Ionic Liquids and Gemini Surfactant: A Detailed Investigation into the Role of Ionic Liquids in Modifying Properties of Aqueous Gemini Surfactant

Tuning physicochemical properties of aqueous surfactant solutions comprised of normal or reverse micelles by external additives is of utmost importance due to the enormous application potential of surfactant‐based systems. Unusual and interesting properties of environmentally benign ionic liquids (IL) make them suitable candidates for this purpose. To understand and establish the role of IL in modifying properties of aqueous gemini surfactants, we studied the effect of the IL, 1‐hexyl‐3‐methylimidazolium bromide ([Hmim][Br]) and 1‐octyl‐3‐methylimidazolium bromide ([Omim][Br]) on the properties of the aqueous cationic gemini surfactant 1,6‐hexanediyl‐α,ω‐bis(dimethyltetradecyl)ammonium bromide (14‐6‐14,2Br^?). The behavioral changes were investigated by measuring the critical micelle concentration (CMC) using electrical conductance, surface tension, dye solubilization and fluorescence probe measurements at 298.15 K. It was observed that the CMC of 14‐6‐14,2Br^? gemini surfactant decreases with addition of IL, thus favoring the micellization process. An increase in micellar size was observed at lower IL concentration using dynamic light scattering, with a decrease in aggregation number (N_agg) determined from fluorescence probe quenching measurements. It is noteworthy that the extent of modulation of the micellar properties is different for both the IL due to their structural differences. IL behave like electrolytes at lower concentrations and cosurfactants at higher concentrations and form mixed micelles with the cationic gemini surfactant showing an increase in N_agg.     

Surface and Aggregation Properties of Synthesized Cetyl Alcohol Based Bis-Sulfosuccinate Gemini Surfactants in Aqueous Solution

A series of cetyl alcohol based anionic bis‐sulfosuccinate gemini surfactants (BSGSCA1,4; BSGSCA1,6 and BSGSCA1,8) with different spacer lengths was prepared using dibromoalkanes. The surfactant structure was elucidated using elemental analysis, Fourier transform infrared spectroscopy (FT‐IR) and nuclear magnetic resonance spectroscopy (NMR). Surface tension measurements were used to determine the critical micelle concentration (CMC), the surface tension at the CMC (γ_CMC), surface pressure at the CMC (π_CMC) and efficiency of adsorption (pC20). On the basis of surface studies, the CMC and γ_CMC decreases with increasing length of the spacer group. The micelle aggregation number, determined by fluorescence quenching studies, increases with increasing surfactant concentration above the CMC. The micropolarity in the micelle increases with increasing length of the spacer and decreases with increasing surfactant concentration.