Academic literature on the topic 'Cationic surfactant CTAB'

The adsorption of cetyltrimethylammonium bromide (CTAB) and nonyl phenyl ethoxylates (NP-n, where n = 13, 20 and 30) on to polystyrene powder has been studied. Concentrations of surfactant solutions ranging from below CMC to well above CMC were investigated. In a single surfactant system, only the cationic surfactant (CTAB) was found to adsorb appreciably while nonionic surfactants showed negligible adsorption. In mixed surfactant systems, the cationic surfactant was found to induce significant co-adsorption of non-ionic surfactants. The increased adsorption of non-ionic surfactants has been attributed to the formation of non-ideal mixed hemimicelles due to intercomponent lateral interactions. However, non-ionic surfactants with longer hydrophilic chains did not form mixed hemimicelles with CTAB. In general, zeta potential measurements support the adsorption results.

AbstractThe interaction of Procaine hydrochloride (PC) with cationic, anionic and non-ionic surfactants; cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS) and triton X-100, were investigated. The effect of ionic and non-ionic micelles on solubilization of Procaine in aqueous micellar solution of SDS, CTAB and triton X-100 were studied at pH 6.8 and 29°C using absorption spectrophotometry. By using pseudo-phase model, the partition coefficient between the bulk water and micelles, Kx, was calculated. The results showed that the micelles of CTAB enhanced the solubility of Procaine higher than SDS micelles (Kx = 96 and 166 for SDS and CTAB micelles, respectively) but triton X-100 did not enhanced the solubility of drug because of weak interaction with Procaine. From the resulting binding constant for Procaine-ionic surfactants interactions (Kb = 175 and 128 for SDS and CTAB surfactants, respectively), it was concluded that both electrostatic and hydrophobic interactions affect the interaction of surfactants with cationic procaine. Electrostatic interactions have a great role in the binding and consequently distribution of Procaine in micelle/water phases. These interactions for anionic surfactant (SDS) are higher than for cationic surfactant (CTAB). Gibbs free energy of binding and distribution of procaine between the bulk water and studied surfactant micelles were calculated.

The surfactant-mediated gelation (SMG) method allows us to formulate hydrogels using a water-insoluble organogelator. In this study, we formulated hydrogels using three cationic surfactants, hexadecyltrimethylammonium bromide (CTAB), hexadecyltrimethylammonium chloride (CTAC), and hexadecylpyridinium chloride (CPC)] and an organogelator (12-hydroxyoctadecanoic acid (12-HOA), and studied their structures and mechanical properties. A fiber-like structure similar to that found in the 12-HOA-based organogels was observed by optical microscopy. Small- and wide-angle X-ray scattering profiles showed Bragg peaks derived from the long- and short-spacing of the crystalline structures in the gel fibers and a correlation peak from the surfactant micelles in the small-angle region. Furthermore, the formation of micelles in the hydrogels was confirmed by UV-vis spectroscopic measurements of the gel samples in the presence of Rhodamine 6G. We concluded that the hydrogels prepared by the SMG method in the present systems are orthogonal molecular assembled systems in which two different molecular assembled structures coexist. Among the three surfactant systems, the CTAB system presented the lowest critical gelation concentration and highest sol-gel transition temperature and viscoelasticity. These differences in gel fiber formation and gel properties were discussed from the viewpoint of the degree of solubilization of the gelator molecules in micelles coexisting with gel fibers and diffusion of the gelator molecules in the gel formation process.

The adsorption behaviours of cetyltrimethylammonium bromide (CTAB) and dioctyl sodium sulphosuccinate (AOT) on fluorite mineral were analyzed as examples of the adsorption of cationic and anionic surfactants on salt-type minerals. Although both surfactants gave adsorption densities well below the monolayer capacity, there were considerable differences between the behaviours of the two surfactants. Thus, while the adsorption density of CTAB increased to a plateau value, that of AOT increased to a maximum before decreasing to very low values at high equilibrium concentrations of the surfactant. Analysis of the behaviour of the surfactants was made using a modified version of the Frumkin adsorption isotherm, taking into account the cross-sectional area of the adsorbed surfactant species and the lateral interaction between their long hydrocarbon chains. The values of the free energy change indicated that both CTAB and AOT underwent adsorption via a physical process, while the lateral interaction coefficient was found to be twice as large in the case of AOT as for CTAB for small or moderate coverage. This latter behaviour was attributed to the fact that while CTAB possesses only one hydrocarbon chain per molecule, AOT has two such chains.

In this paper, the enhanced adsorption of methylene blue (MB) dye ion on the activated carbon (AC) modified by three surfactants in aqueous solution was researched. Anionic surfactants—sodium lauryl sulfate (SLS) and sodium dodecyl sulfonate (SDS)—and cationic surfactant—hexadecyl trimethyl ammonium bromide (CTAB)—were used for the modification of AC. This work showed that the adsorption performance of cationic dye by activated carbon modified by anionic surfactants (SLS) was significantly improved, whereas the adsorption performance of cationic dye by activated carbon modified by cationic surfactant (CTAB) was reduced. In addition, the effects of initial MB concentration, AC dosage, pH, reaction time, temperature, real water samples, and additive salts on the adsorption were studied. When Na+, K+, Ca2+, NH4+, and Mg2+ were present in the MB dye solution, the effect of these cations was negligible on the adsorption (<5%). The presence of NO2- improved the adsorption performance significantly, whereas the removal rate of MB was reduced in the presence of competitive cation (Fe2+). It was found that the isotherm data had a good correlation with the Langmuir isotherm through analyzing the experimental data by various models. The dynamics of adsorption were better described by the pseudo-second-order model and the adsorption process was endothermic and spontaneous. The results showed that AC modified by anionic surfactant was effective for the adsorption of MB dye in both modeling water and real water.

A novel, simple, low-cost, and user-friendly potentiometric surfactant sensor based on the new 1,3-dihexadecyl−1H-benzo[d]imidazol−3-ium-tetraphenylborate (DHBI–TPB) ion-pair for the detection of cationic surfactants in personal care products and disinfectants is presented here. The new cationic surfactant DHBI-Br was successfully synthesized and characterized by nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR) spectrometry, liquid chromatography–mass spectrometry (LC–MS) and elemental analysis and was further employed for DHBI–TPB ion-pair preparation. The sensor gave excellent response characteristics for CTAB, CPC and Hyamine with a Nernstian slope (57.1 to 59.1 mV/decade) whereas the lowest limit of detection (LOD) value was measured for CTAB (0.3 × 10−6 M). The sensor exhibited a fast dynamic response to dodecyl sulfate (DDS) and TPB. High sensor performances stayed intact regardless of the employment of inorganic and organic cations and in a broad pH range (2−11). Titration of cationic and etoxylated (EO)-nonionic surfactant (NSs) (in Ba2+) mixtures with TPB revealed the first inflexion point for a cationic surfactant and the second for an EO-nonionic surfactant. The increased concentration of EO-nonionic surfactants and the number of EO groups had a negative influence on titration curves and signal change. The sensor was successfully applied for the quantification of technical-grade cationic surfactants and in 12 personal care products and disinfectants. The results showed good agreement with the measurements obtained by a commercial surfactant sensor and by a two-phase titration. A good recovery for the standard addition method (98–102%) was observed.

The interaction betweenλ—DNA and cationic surfactants with varying alkyl chain lengths was investigated. By dynamic light scattering method, the trimethyl-ammonium bromides-DNA complex formation was shown to be dependent on the length of the surfactant’s alkyl chain. For surfactants with sufficient long alkyl chain (CTAB, TTAB, DTAB), the compacted particles exist with a size of ~60–110 nm at low surfactant concentrations. In contrast, high concentration of surfactants leads to aggregates with increased sizes. Atomic force microscope scanning also supports the above observation. Zeta potential measurements show that the potential of the particles decreases with the increase of surfactant concentration (CTAB, TTAB, DTAB), which contributes much to the coagulation of the particles. For OTAB, the surfactant with the shortest chain in this study, it cannot fully neutralize the charges of DNA molecules; consequently, the complex is looser than other surfactant-DNA structures.

Amine-containing pharmaceuticals are the most often detected pharmaceuticals in wastewater and ambient aquatic environments. They can usually be degraded by manganese oxide (MnO2), which is a common natural oxidant in soils. Surfactants often coexist with pharmaceuticals in wastewater. Some amine-containing pharmaceuticals, such as diclofenac (DIC), are acidic and are thus ionic compounds in neutral conditions. These compounds, therefore, have similar properties to surfactants. Surfactants, thus, may influence the adsorption and degradation processes of DIC by MnO2. The effect of the type of surfactant on the degradation of DIC by MnO2 was investigated in this study with the addition of two common biodegradable surfactants (cetyltrimethyl-ammonium bromide (CTAB) and sodium dodecylsulfate (SDS)). The results indicated that the cationic surfactant (CTAB) significantly increased the degradation rate in neutral and alkaline conditions. On the other hand, the anionic surfactant (SDS) slightly increased the DIC removal rate in an acidic condition but significantly decreased the removal in neutral and alkaline conditions. Coexisting cationic surfactants not only influenced the kinetics but also altered the transformation mechanism of DIC by MnO2. Decarboxylation is the main transformation mechanism of DIC in the presence of CTAB, while both decarboxylation and hydroxylation are the main transformation mechanisms in the absence of CTAB.

The interaction of an anionic dye (Methyl Orange) with cationic surfactant (Cetyltrimethylammonium Bromide, CTAB) in the series of solvent containing variable compositions of methanol-water mixture (10%, 20%, 30% and 40%) was studied at room temperature (31±2oC). Conductivity measurements were done for the investigation of interaction of dyes. The specific conductance of 6.58x10-5 M to 59.22x10-5M surfactant (CTAB) and these surfactants with 1.008x10-3M dye (MO) mixtures were noted at room temperature. A theoretical model was used to calculate conductance ratio from the data of measured specific conductance values. Values of conductance ratio of CTAB-MO mixtures were found to be all less than 1 which indicated that CTAB-MO dye -surfactant mixture exert significant influence on the degree of interaction.Int. J. Appl. Sci. Biotechnol. Vol 5(2): 172-179

Hydroxyapatite (HAp) particles, a potential starting material for bone substitutes, with nanopores were synthesized in the presence of cetyltrimethylammonium bromide (CTAB) and P123 as cationic and nonionic surfactants as the structuring units. Effect of nonionic surfactant concentration on surface areas is also investigated. Based on N2 adsorption-desorption isotherms investigation, surface area increased up to 50 m2/g by using P123 and 147 m2/g by using CTAB as porosity agent. Pore structure remained even after the removal of surfactant and calcinations at 400°C.

On décrit la préparation de deux séries de 2-hydroxymethylbenzimidazoles substitués par une chaine n-alkyle (1 a 14 carbones) en position 5(6) (série I) ou 1 (série II) ainsi que la mise au point de la synthèse de nouveaux picolinates de 4-nitrophenyle (série III) porteurs d'un groupe alkoxy hydrophobe de 1 a 18 atomes de carbone. L'activité esterolytique des systèmes ligands I ou II-Zn2+ vis-à-vis des esters actives III en présence de micelles cationiques (CTAB) est comparée à celle d'un système hydrosoluble de même nature. L'étude cinétique montre l'intervention d'un seul complexe actif 2/1 pour la série I, mais de deux complexes actifs 1/1 et 2/1 pour la série II alors qu'en l'absence de micelles n'existe que le complexe 1/1. Le pouvoir esterolytique global de ces complexes est beaucoup plus élevé qu'une solution moléculaire. L'étude plus détaillée d'un ligand I montre sa complexation quasi totale; cependant la constante de vitesse apparente liée au complexe ainsi que les constantes spécifiques rapportées à la pseudo-phase micellaire sont plus faibles qu'en l'absence de micelle. Cette forte diminution de réactivité peut être attribuée à la formation plus difficile du complexe ternaire ligand/-Zn++/ester, intermédiaire dans la réaction d'esterolyse

Ce travail est consacré à l'élaboration par voie humide (pontage, solvothermale et colloïdale) de photocatalyseur TiO2 supporté sur trois types de minéraux argileux d'origine marocaine: la stévensite, la beidellite et la palygorskite, à leurs caractérisations et finalement à l'évaluation de leurs activités photocatalytiques vis-à-vis de l'élimination en milieu aqueux du colorant anionique l'Orange G (OG) très utilisé en industrie textile. La stévensite et la beidellite sont toutes les deux des smectites de types magnésien trioctaédrique et aluminifère dioctaédrique respectivement. En revanche, la palygorskite est un minéral fibreux riche en Al doté d'un caractère dioctaédrique très marqué. Les matériaux photocatalyseurs supportés développés par le pontage de la stévensite ou de la beidellite ne révèlent pas de formation de piliers interlamellaires de TiO2, mais plutôt l'obtention dans les deux cas de matrice de TiO2 amorphe dans laquelle sont éparpillées quelques rares particules indemnes de phyllosilicates. De même, ceux à base de stévensite élaborés par la méthode solvothermale révèlent des particules du phyllosilicate désintégrées au sein d'une matrice de TiO2 toutefois cristallisée sous forme d'anatase. Néanmoins, la fonctionnalisation selon la voie colloïdale a permis d'immobiliser avec succès des nanoparticules d'anatase (10 nm) sur aussi bien des feuillets plus ou moins exfoliés de stévensite ou de beidellite que sur des fibres de palygorskite. L'anatase attachée aux particules de ces minéraux argileux demeure extraordinairement stable jusqu'à 900 °C alors que celle formée en absence de ces phyllosilicates se convertit complètement en rutile vers 650 °C. Cette stabilité remarquable de l'anatase supportée est due à l'empêchement de la croissance, par coalescence à haute température, de la taille de ses particules au-delà de la taille critique (30 nm) requise pour sa conversion en rutile relativement moins photoactive. Les essais de photocatalyse révèlent que l'activité catalytique des différents matériaux élaborés croit selon la méthode de fonctionnalisation: pontage - méthode solvothermale - voie colloïdale et aussi selon la nature du minéral argileux : stévensite - beidellite - palygorskite. En outre, les matériaux photocatalyseurs supportés, à base de beidellite ou de palygorskite, développés par la voie colloïdale, manifestent une activité deux fois supérieure à celle de la poudre commerciale TiO2 Degussa P25. Leurs particules floculent aisément, ce qui facilite leur élimination du milieu aqueux sans recourir à la microfilitration requise dans le cas de la Degussa P25
This work was devoted to the elaboration by wet route (pillaring, solvothermal and colloidal) of TiO2 supported photocatalysts on three kinds of clay minerals (stevensite, beidellite and palygorskite) from Morocco, to their characterizations and finally to the evaluation of their photocatalytic activities towards the removal from aqueous media of anionic Orange G dye, widely used in textile industry. Stevensite and beidellite were magnesian trioctahedral and aluminiferous dioctahedral smectites respectively. Nevertheless, palygorskite was a fibrous Al-rich clay mineral with a predominant dioctahedral character. The photocatalyst materials elaborated by the pillaring of stevensite or beidellite did not reveal the formation of TiO2 interlayer pillars, but the observation of an amorphous matrix of Ti-rich phase within which were distributed some rare unaltered particles of phyllosilicates. Those based on stevensite elaborated according to solvothermal method also showed dissolved phyllosilicates particles, but within crystalline TiO2 anatase matrix. Nevertheless, the functionalized materials developed according to colloidal route exhibited successful immobilization of anatase nanoparticles (10 nm) onto as well as more or less exfoliated layers of stevensite or beidellite than on palygorskite fibers. Anatase remained remarkably stable up to 900 °C when attached to particles of clay minerals in comparison with that developed in their absence which underwent a complete transformation into rutile at around 650°C. This remarkable stability at high temperature of anatase supported on clay minerals particles was due to the hindrance of particles growth by sintering whose the sizes remained below the nucleus critical sizes (30 nm) required for its transition into less photoactive rutile. The photocatalysis tests revealed that the catalytic activity of different elaborated materials increased according to the synthesis route: pillaring process - solvothermal method - colloidal route and according to the nature of clay mineral: stevensite - beidellite - palygorskite. In addition, the supported photocatalysts based on beidellite or palygorskite prepared by colloidal route were found to be twice more active than the commercial TiO2 powder Degussa P25. Furthermore, their particles easily floculated so that they are readily removable from treated solutions without resorting to expensive microfiltration required upon the use of Degussa P25

A quality by design approach was used to investigate the influence of formulation composition and spray drying conditions on physicochemical properties of redispersable lipid based nanosystems loaded with Syzygium aromaticum essential oil. Four critical independent variables were studied: presence or absence of the liquid lipid oleic acid (0% - 1%), of the cationic surfactant CTAB (0% and 1%), inlet drying temperature (60 ºC -80 ºC), and ratio of the drying aids (ADJ) regarded to total formulation constituents weight (1:1 and 2:1). Resuls showed the production of spray dried redispersable lipid systems loaded with essential is feasible under very restrict conditions. Keywords: Encapsulation; lipid systems; essential oil; spray drying; redispersable.

Abstract Given the increasing demand for energy globally and depleting oil and gas resources, it is crucial to increase the production from existing reservoirs by introducing new technologies for Improved/Enhanced Oil Recovery (IOR/EOR). This contribution presents a novel hybrid IOR/EOR method, which combines smart water (SW) and foam flooding, known as Smart Water Assisted Foam (SWAF) flooding. The optimal conditions of the SWAF technology will be interpreted using experimental laboratory design (i.e., experimental data). The experimental design was divided into three main steps. The first step is obtaining rock wettability measurements using contact angle measurements. This step aims to select the optimum SW composition that changes the carbonate rock's wettability from oil-wet towards more water-wet and faster oil recoveries. The water-wet condition leads to high residual oil saturations and low end-point permeabilities. This is conductive to favourable mobility ratios and efficient water-oil displacement. However, high residual oil saturations are unfavourable to the high ultimate oil recovery as much oil stays behind. Secondly, the chemical screening follows, where two tests were performed, viz., (i) an Aqueous Stability Test (AST), (ii) and a Foamability and Foam Stability Tests (FT/FST). This step aims to generate a stable foam (i.e., surfactant aqueous solution + gas) in the absence and presence of crude oil with different TAN (Total Acid Number) and TBN (Total Base Number), viz., crude oils Type-A and Type-B. Favourable mobility ratio is achieved by the presence of foam, which leads to excellent displacement efficiency. Thirdly, core flooding tests are performed. This step aims to select the best formulations through SWAF core flooding tests to obtain the ultimate recovery factor under different injection scenarios. The optimal SWAF condition combines high ultimate recovery with the best displacement efficiency. It is shown that the enormous changes in wettability were seen for SW (MgCl2) solution at 3500 (ppm) for both crude oils Type-A and Type-B. It has been shown that the use of a cationic surfactant CTAB (i.e., cetyltrimethylammonium-bromide) in the positively charged carbonates (with an isoelectric point of pH = 9) is more effective than the use of anionic surfactant, e.g., Alpha Olefin Sulfonate (AOS). The aim is to create an optimum surfactant aqueous solution (SAS). The SAS stability is considerably affected by the concentration of both the SW (MgCl2) and surfactant (CTAB). In the absence of oil, the strength of foam (SAS and Gas) is highly dependent on the concentration and composition of the SW in the SAS. In the presence of oil, foam generation and stability are better when the crude oil has a low TAN and high TBN. From the core flooding tests for crude oils Type-A and Type-B, the ultimate residual oil recovery was achieved by the MgCl2 - foam injection combination (i.e., incremental oil recovery of 42%, which is equivalent to a cumulative oil recovery of 92%). In summary, SWAF under the optimum conditions is a promising method to increase the oil recovery from carbonate reservoirs.

Shear viscosities of one kind of turbulent drag-reducing cationic surfactant solution, Cetyltrimethyl ammonium chloride (CTAC)/Sodium salicylate (NaSal) aqueous solution, were experimentally investigated by use of a stress controlled Reometer. The concentration and temperature of the solution ranged from 50 to 200 ppm and 20 to 40°C, respectively. The Giesekus model was found to fit the measured shear viscosities well for different temperatures and concentrations of the surfactant solution and the model parameter values obtained by fitting were correlated with temperature at certain solution concentrations. The temperature was found to have a large influence on the viscoelasticity of the surfactant solution. By using the model parameters obtained from the correlations, 70 percent of the measured shear viscosities agreed with the prediction by the Giesekus model within ±27.3 percent. The elongational viscosities of CTAC/NaSal surfactant solution were also experimentally investigated by use of an oppositing jet Reometer. The measured data were lower than the prediction by the Giesekus model.

In this paper, two-oscillating grid turbulence with/without viscoelastic additives was performed experimentally by particle image velocimetry. Two classical drag-reducing additives-polymer (Polyacrylamide, PAM) and cationic surfactant (cetyltrimethyl ammonium chloride, CTAC) were chosen. The experiments were carried out under the classical concentration (25ppm) and three different grid oscillation frequencies. Two-dimensional wavelet transform was utilized to investigate multi-scale characteristics of vortex structures and intermittency based on wavelet coefficient. The results showed that at the same decomposition level, the existence of viscoelastic additives attenuates the high-frequency components of fluctuation velocity. The small-scale intermittency is remarkably inhibited by viscoelastic additives especially for scale parameter smaller than 24. Besides, CTAC additives show different effect from PAM additives. Therefore, turbulent drag reduction with additives also happens in two-oscillating grid turbulence without wall effect.

An experimental investigation was performed on the swirling flow of viscoelastic fluid with deformed free surface in a cylindrical container driven by the constantly rotating bottom wall. The tested fluid was an aqueous solution of CTAC (cetyltrimethyl ammonium chloride), which is a cationic surfactant. Water, 40ppm, 60ppm and 200ppm CTAC solution flows were tested at Froude numbers ranging from 2.59 to 16.3. PIV was used to measure the secondary velocity field in the meridional plane and the deformed free-surface level was extracted from the PIV images. At a similar Froude number, the depth of the dip formed at the center region of the free surface was decreased for CTAC solution flow compared with water flow. The inertia-driven vortex at the up-right corner in the meridional plane becomes more and more weakened with increase of the solution concentration or viscoelasticity. Through analyzing the overall force balance compared with water flow, the first normal stress difference or the weak viscoelasticity was estimated for the dilute CTAC solution flows.