Didodecyldimethylammonium Bromide Research Articles

Vesicle‐to‐micelle transition in aqueous mixtures of cationic lipids with Pluronic F127

AbstractAqueous solutions of vesicle‐forming lipids mixed with micelle‐forming copolymers may result in stabilized and biocompatible aggregates. Differential scanning calorimetry (DSC) and dynamic light scattering (DLS) techniques were used here to investigate the effects of the nonionic triblock copolymer Pluronic F127 (F127) on the thermal behavior, structural changes, and hydrodynamic size of cationic vesicles from dioctadecyldimethylammonium chloride (DODAC), dioctadecyldimethylammonium bromide (DODAB), and didodecyldimethylammonium bromide (DDAB) in aqueous dispersion. The DSC thermograms indicate that upon the addition of up to 5.0 mM F127, a vesicle‐to‐micelle transition occurs in three stages. First, there is a predominance of lipid‐F127 mixed vesicles, followed by the co‐existence of mixed vesicles and micelles, and finally, the system is dominated by mixed micelles. DLS results reveal that with the addition of F127 to the lipid dispersions, the size of the assembled structures tends to decrease, also indicating structural changes of vesicles to micelles. These results indicate that the borders between these stages depend on the lipid chain length and counterion type.

Controllable synthesis of bowl-shaped porous carbon materials through didodecyldimethylammonium bromide for high performance supercapacitors

Controllable synthesis of bowl-shaped porous carbon materials through didodecyldimethylammonium bromide for high performance supercapacitors

Electrohydrodynamically Printed High‐resolution Arrays Based on Stabilized CsPbBr3 Quantum Dot Inks

AbstractHigh‐resolution perovskite quantum dots (PeQDs) arrays printed by electrohydrodynamic (EHD) inkjet printing show great application prospects in fields of micro‐display. Commonly, EHD inkjet requires a polar system for printing but it easily quenches the PeQDs. Meanwhile, the mismatch of solvent parameters causes uneven surface morphology and printing instability. In this work, a morphology uniformization strategy of a nonpolar binary solvent system of 1,3,5‐triethylbenzene and n‐tetradecane is proposed to prepare the didodecyldimethylammonium bromide (DDAB)/PbBr2 passivated PeQDs inks. When the solvent volume ratio is 5:5, the photoluminescence quantum yield (PLQY) of the ink reaches 94.06%. Benefiting from the match of boiling point, surface tension, and dielectric constant of ink, after the EHD inkjet printing, the line width of continuous smooth line arrays is as narrow as 2.0 µm and the coffee effect of dot arrays is well inhibited. Meanwhile, derived from the strong electrostatic interaction between the π‐electron structure of 1,3,5‐triethylbenzene and DDA+, the ink exhibits high stability. Moreover, the high‐resolution logo and miniature quick responsecode by EHD inkjet printing reach 22 718 dpi, far higher than that of the reported micro‐LED. This work paves the way for high‐resolution pixel arrays of micro‐display.

Rationalizing the Design of Pluronics-Surfactant Mixed Micelles through Molecular Simulations and Experiments.

Aqueous systems comprising polymers and surfactants are technologically important complex fluids with tunable features dependent on the chemical nature of each constituent, overall composition in mixed systems, and solution conditions. The phase behavior and self-assembly of amphiphilic polymers can be changed drastically in the presence of conventional ionic surfactants and need to be clearly understood. Here, the self-aggregation dynamics of a triblock copolymer (Pluronics L81, EO3PO43EO3) in the presence of three cationic surfactants (with a 12C long alkyl chain but with different structural features), viz., dodecyltrimethylammonium bromide (DTAB), didodecyldimethylammonium bromide (DDAB), and ethanediyl-1,2-bis(dimethyldodecylammonium bromide) (12-2-12), were investigated in an aqueous solution environment. The nanoscale micellar size expressed as hydrodynamic diameter (Dh) of copolymer-surfactant mixed aggregates was evaluated using dynamic light scattering, while the presence of a varied micellar geometry of L81-cationic surfactant mixed micelles were probed using small-angle neutron scattering. The obtained findings were further validated from molecular dynamics (MD) simulations, employing a simple and transferable coarse-grained molecular model based on the MARTINI force field. L81 remained molecularly dissolved up to ∼20 °C but phase separated, forming turbid/translucent dispersion, close to its cloud point (CP) and existed as unstable vesicles. However, it exhibited interesting solution behavior expressed in terms of the blue point (BP) and the double CP in the presence of different surfactants, leading to mixed micellar systems with a triggered morphology transition from unstable vesicles to polymer-rich micelles and cationic surfactant-rich micelles. Such an amendment in the morphology of copolymer nanoaggregates in the presence of cationic surfactants has been well observed from scattering data. This is further rationalized employing the MD approach, which validated the effective interactions between Pluronics-cationic surfactant mixed micelles. Thus, our experimental results integrated with MD yield a deep insight into the nanoscale interactions controlling the micellar aggregation (Pluronics-rich micelles and surfactant-rich micelles) in the investigated mixed system.

Strongly Confined CsPbBr3 Quantum Dots as Quantum Emitters and Building Blocks for Rhombic Superlattices.

The success of the colloidal semiconductor quantum dots (QDs) field is rooted in the precise synthetic control of QD size, shape, and composition, enabling electronically well-defined functional nanomaterials that foster fundamental science and motivate diverse fields of applications. While the exploitation of the strong confinement regime has been driving commercial and scientific interest in InP or CdSe QDs, such a regime has still not been thoroughly explored and exploited for lead-halide perovskite QDs, mainly due to a so far insufficient chemical stability and size monodispersity of perovskite QDs smaller than about 7 nm. Here, we demonstrate chemically stable strongly confined 5 nm CsPbBr3 colloidal QDs via a postsynthetic treatment employing didodecyldimethylammonium bromide ligands. The achieved high size monodispersity (7.5% ± 2.0%) and shape-uniformity enables the self-assembly of QD superlattices with exceptional long-range order, uniform thickness, an unusual rhombic packing with an obtuse angle of 104°, and narrow-band cyan emission. The enhanced chemical stability indicates the promise of strongly confined perovskite QDs for solution-processed single-photon sources, with single QDs showcasing a high single-photon purity of 73% and minimal blinking (78% "on" fraction), both at room temperature.

Nonpolar and Ultra-long-chain Ligand to Modify the Perovskite Interface toward High-Efficiency and Stable Wide Bandgap Perovskite Solar Cells

Though tandem solar cells (TSCs) based on wide-bandgap perovskite solar cells (WB-PSCs) as the top sub-cells continuously gain efficiency breakthroughs, the low power conversion efficiency (PCE) of WB-PSCs caused by the defects and interface energy-level mismatch is still a vital issue limiting their performance. Moreover, the stability of the perovskite layer against the moisture and subsequent fabrication process is essential to highly stable TSCs. Herein, a nonpolar material with an ultra-long chain, didodecyldimethylammonium bromide (DDAB), was introduced to WB-PSCs as an interface material for reducing the surface defects and increasing the surface hydrophobicity of the perovskite layer. The DDAB-modified perovskite surface is much more hydrophobic, with a water contact angle of 104.9°. Systemically experimental studies reveal that apart from the passivation on the point defects, DDAB can suppress the formation of PbI2 aggregates, smoothing the perovskite surface and shifting the energy level upward. As a result, the 1.74 eV WB-PSCs with inverted structures exhibit a champion PCE of 18.74% by DDAB modification, compared to the standard device with a PCE of 16.50%. The device stability under a relative humidity of >85% is apparently enhanced by 5-fold. This work provides a concept of screening interface materials for highly efficient and stable WB-PSCs.

Complementary ligand decorated cesium lead bromide nanoplatelets for high performance light-emitting diodes

Two dimensional cesium lead bromide (CsPbBr3) nanoplatelets (NPLs) have gained numerous attention due to its tunable thickness, large exciton binding energy and excellent optical properties which can be applied in various photoelectric device. However, synthesizing blue emitting NPLs with long-term stability and high photoluminescence quantum yields (PLQYs) was still difficult. Here, we demonstrate a strategy based on surface ligand engineering, using didodecyldimethylammonium bromide and sodium dodecylbenzene sulfonate as surface ligands to impart higher PLQYs to perovskite materials while improving the stability of CsPbBr3 NPLs. These ligands strongly interact with CsPbBr3 NPLs, compared with untreated materials, effectively eliminating defects on the surface of NPLs and significantly improving the structural stability of perovskite materials. High-quality CsPbBr3 NPLs with high color purity (narrow peaks located at ∼470 nm) and PLQYs up to 90 % were prepared by this method. In addition, the stability of treated NPLs under some harsh environments (including long-term storage, high temperature and 365 nm UV light irradiation) has been significantly improved. White light-emitting diodes were finally fabricated using these highly bright and stable CsPbBr3 NPLs.

Effect of a double-chain surfactant on the stabilization of suspensions of silica and titania particles against agglomeration and sedimentation

Dispersions of vesicles of didodecyldimethylammonium bromide (DDAB) were prepared with magnetic stirring of multilamellar liposomes followed by ultrasonication (SS) in order to generate dispersions that contained only unilamellar vesicles, unlike the stirring-only (S) method which also produces many large liposomes. With the SS method, the vesicles had average diameters ranging from 68 to 80 nm, which were much smaller than the diameters generated with the S method. The new vesicle dispersions had nearly infinite viscosities at very low shear stresses at DDAB weight fractions wD from 0.025 to 0.027, even though they were not close-packed, in contrast to the S dispersions. The new SS vesicle dispersions stabilized completely against sedimentation polydisperse nonspherical crystalline titania particles with sizes ranging from ca. 96–156 nm, as well as suspensions of monodisperse spherical amorphous silica particles with diameters of dsed = 454 nm, 691 nm, and 826 nm. These results establish that DDAB vesicle dispersions can stabilize against sedimentation a broad range of particle types and sizes. In addition, at the low values of wD = 0.009 and 0.018, the effective viscosities, ηeff, of the DDAB dispersions, determined from the sedimentation velocities, ranged from 1.35-1.87 cP and 4.34–5.57 cP, respectively. At higher shear stresses, however, these dispersions were highly shear-thinning and still flowable in a capillary under gravity. This behavior is critical for the practical applications of such dispersions for inkjet printing and possibly paints.

Influence of surfactant on glass transition temperature of poly(lactic-co-glycolic acid) nanoparticles.

Poly(D,L-lactic-co-glycolic acid) (PLGA) is one of the most commonly used drug carriers in nanomedicines because of its biodegradability, biocompatibility and low toxicity. However, the physico-chemical characterization and study of drug release are often lacking the investigation of the glass transition temperature (Tg), which is an excellent indicator of drug release behavior. In addition, the residual surfactant used during the synthesis of nanoparticles will change the glass transition temperature. We thus prepared PLGA nanoparticles with polymeric (poly(vinyl alcohol) (PVA)) and ionic (didodecyldimethylammonium bromide (DMAB)) surfactant to investigate their influence on the glass transition temperature. Determination of Tg in dry and wet conditions were carried out. The use of concentrated surfactant during synthesis resulted in a larger amount of residual surfactant in the resulting particles. Increasing residual PVA content resulted in an increase in particle Tg for all but the most concentrated PVA concentrations, while increasing residual DMAB content resulted in no significant change in particle Tg. With the presence of residual surfactant, the Tg of particle and bulk samples measured in wet conditions is much lower than that in dry conditions, except for bulk PLGA containing the ionic surfactant, which may be related to the plasticizing effect of the DMAB molecules. Notably, the Tg of both particles in wet conditions is approaching physiological temperatures where subtle changes in Tg could have dramatic effects on drug release properties. In conclusion, the selection of surfactant and the remaining amount of surfactant are crucial parameters to utilize in designing the physico-chemical properties of PLGA particles.

Rheology of graphene oxide stabilized Pickering emulsions.

Pickering emulgels stabilized by graphene oxide (GO) with didodecyldimethylammonium bromide (DDAB) as an auxiliary surfactant and liquid paraffin as the oil phase have proved to be an excellent 3D printable ink. This paper elucidates the structure of such emulgels by a combination of microscopy before and after intensive shear as well as broadband dielectric spectroscopy and rheology in the linear and nonlinear regime. An increase of the DDAB surfactant and GO-contents leads to a systematic increase of modulus and viscosity, a reduction of the limits of the nonlinear regime and a more complicated variation of the normal forces, with negative normal forces at high shear rate  for low GO-contents and positive normal forces at high GO-contents. The interfacial jamming behavior studied by morphology, rheology and dielectric spectroscopy is explained based on droplet deformation, jamming and recovery phenomena.

Protein-induced transformation of unilamellar to multilamellar vesicles triggered by a polysaccharide

We report on the morphological transitions of didodecyldimethylammonium bromide (DDAB) cationic vesicles and hybrid DDAB/hyaluronic acid (HA) vesicles upon addition of BSA at pH 7 where BSA is overall negatively charged. Small angle neutron scattering (SANS) is used to extract the size distributions of the nanovesicles, the thickness of the DDAB bilayers and their lamellarity. Although the HA-decorated DDAB vesicles contain the negatively charged polysaccharide the interaction with BSA appears to be more intense in comparison to bare vesicles. Characteristic peaks in the SANS patterns indicate the presence of multilamellar interfaces while the formation of multilamellar vesicles induced by BSA depends on the amount of added HA. Consequently, higher lamellarities are observed at higher BSA contents. This work demonstrates a simple methodology to tune the encapsulation of globular proteins in vesicular nanoassemblies by affecting their lamellarity and has direct implications on the application of vesicles and liposomes in protein delivery.

Synergistic Effects of Surface Ligand Engineering and Double Matrices Protecting Enable Ultrastable and Highly Emissive Blue/Cyan Perovskite Nanocrystal Films for Multifunctional Applications

AbstractPerovskite nanocrystals (NCs) have attracted considerable attention because of the extraordinary optoelectronic properties, making them promising candidates for lighting and display applications. However, the emissive efficiency and stability of blue/cyan‐emitting NCs lag far behind other color emissive perovskites, which greatly restrict their practical application. Herein, a feasible strategy is proposed for synthesizing highly luminescent and stable CsPbClxBr3−x NCs by the didodecyldimethylammonium bromide (DDAB) ligand‐assisted post‐treatment. The prepared DDAB‐CsPbCl0.8Br2.2 and DDAB‐CsPbCl2.0Br1.0 NCs exhibit bright cyan and blue emission, respectively, and their quantum yields are significantly enhanced from 12.2% and 7.5% to 83.1% and 75.3% owing to the obvious decrease of surface defects by the ligand‐exchange and halogen‐compensation mechanisms. The outstanding fluorescence properties are almost remained by grafting perovskite NCs onto the surface of SiO2 nanospheres. Notably, the ultrahigh water‐stability is realized after encapsulating the composite nanospheres into polystyrene‐polyisoprene‐polystyrene (SIS) film, which is benefit from the triple protection of DDA+ cations, SiO2 nanospheres and SIS copolymers. The fabricated SiO2@DDAB‐CsPbCl2.0Br1.0/SIS film is assembled into an white light emitting diode with high color rendering index of 83.4. Importantly, the blue/cyan‐emitting films display superb temperature‐sensitivity (30–160 °C) and favorable elasticity (1200% stretch rate), indicating their promising application prospect in flexible multifunctional photoelectric devices.

Enhanced Charge Transfer Kinetics for the Electroreduction of Carbon Dioxide on Silver Electrodes Functionalized with Cationic Surfactants

AbstractCationic ammonium surfactants can be used together with a suitable catalyst to enhance the electroreduction of carbon dioxide (CO2RR). However, the underlying reasons for the improvements are not yet well understood. In this study, it is shown that didodecyldimethylammonium bromide (DDAB; [(C12H25)2N(CH3)2]Br), when added to the catholyte, can increase the rate of CO2 reduction to CO on silver electrodes by 12‐fold at −0.9 V versus reversible hydrogen electrode. More importantly, electrochemical impedance spectroscopy revealed that DDAB lowers the charge transfer resistance (RCT) for CO2RR on silver, and these changes can be correlated with enhancements in partial current densities of CO. Interestingly, when DDAB is added onto two other CO‐producing metals, namely, zinc and gold, the CO2RR charge transfer kinetics are improved only on Zn, but not on Au electrodes. By means of a semiempirical model combining density functional theory calculations and experimental data, it is concluded that DDAB generally strengthens the adsorption energies of the *COOH intermediate, which leads to enhanced CO production on silver and zinc, but not on gold.

Influence of Cellulose Nanofibers on the Behavior of Pickering Emulsions. Part 1. Microscopy and Startup Flow Test

The dispersibility of flexible polymer chains present at the emulsion's interface between the dispersed and continuous phase has obvious effects on rheology and dielectric properties of the whole emulsion. Cellulose nanofiber (CNF)-based Pickering emulsions are good systems to research these properties with respect to their microscopic phase structure, dielectric, and rheological properties by using CNF as a water-dispersible Pickering emulsifier, liquid paraffin as an oil phase, and didodecyldimethylammonium bromide (DDAB) as a cationic auxiliary surfactant. The CNF and DDAB contents were systematically varied while the water-to-paraffin oil ratio was kept constant to discern the influence of the Pickering emulsifiers. Polarized optical microscopic images reveal that the droplets tend to shrink at higher CNF content but grow bigger when increasing the DDAB content, which is proved by fluorescence analysis of the CNF dispersibility with varying DDAB content. The dielectric damping exhibits a minimum, whose value decreases with increasing DDAB and CNF content. Increasing the DDAB content promotes the solubilization of CNF in the aqueous phase, which will increase the overall viscosity and yield points. Similarly, a higher CNF content leads to a higher viscosity and yield point, but at high DDAB contents, the viscosity function exhibits an S-shape at intermediate CNF contents. To evaluate the results further, they were compared with CNF dispersions (without oil phase), which showed a surfactant effect slightly on maximum stress but strongly on yield stress τy, indicating that DDAB can promote the formation of a CNF network rather than the viscosity of the whole system. This paper provides information on how a systematical variation of the composition influences morphology and physico-chemical interactions as detected by broadband dielectric spectroscopy and rheological behavior.

Effects of Fe3O4 Magnetic Nanoparticle Functionalization with Ionic Liquids and a Double-Chained Surfactant on the Pretreatment of Plasma Samples during Drug Extraction.

Ionic liquids (ILs), also known as "designer solvents," comprise a large group of compounds that can improve overall sample preparation performance due to their unique physical and chemical properties. Some of them have a comparable structure to surfactants, which can be also considered as effective extraction solvents. In this study, nine different ILs and a double-chained surfactant were investigated as potential coating materials for iron oxide-based nanoparticles (NPs) used in the pretreatment of human plasma samples. Various methods of synthesizing and functionalizing NPs were employed in fabricating the magnetic sorbents, with the physicochemical properties of the resultant extraction phases (i.e., naked NPs, NPs coated with silica, and NPs coated with silica and selected IL or surfactant) being characterized via X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TG), and transmission electron microscopy (TEM). The effectiveness of the developed NP-based extraction phases was tested by applying them for the extraction of epirubicin hydrochloride (EPI) from plasma samples, followed by analysis via liquid chromatography with fluorescence detection (LC-FL). The results showed that NPs coated with both silica and IL or silica and surfactant provided significantly higher extraction efficiency compared to naked NPs and NPs coated solely with silica. Additionally, the findings also revealed that the adsorption of analytes depends not only on the coating procedure but also on the type of coating material used to functionalize the NPs. Among the tested structures, didodecyldimethylammonium bromide provided the best performance for the functionalization of NP sorbents previously coated with silica.

Anion-Exchange Blue Perovskite Quantum Dots for Efficient Light-Emitting Devices.

In this study, blue perovskite quantum dots (PQDs) were prepared using didodecyldimethylammonium bromide (DDAB), which can passivate surface defects caused by the loss of surface ligands and reduce particle size distribution. After the passivation of DDAB, blue CsPbClxBr3-x PQDs dispersed in n-octane produced a more compact and uniform PQD thin film than the non-passivated ones. The resulting device showed a stabile lifetime, and an EL peak of 470 nm and a maximum EQE of 1.63% were obtained at an operating voltage of 2.6 V and a current density of 0.34 mA/cm2. This work aims to provide a simple method to prepare blue-emitting PQDs and high-performance PQD-based light-emitting devices.

Increasing the Efficiency of Cytochrome P450 3A4 Electrocatalysis Using Electrode Modification with Spatially Ordered Anodic Aluminum Oxide-Based Nanostructures for Investigation of Metabolic Transformations of Drugs.

A new approach for modifying electrodes using porous membranes based on anodic aluminum oxide with pore diameters of 0.1 and 0.2 µm and a membrane-like substance didodecyldimethylammonium bromide (DDAB) was proposed to study the electrocatalytic efficiency of the system. This approach makes it possible to increase the catalytic efficiency of the cytochrome P450 3A4-dependent N-demethylation of erythromycin by 132% when using a membrane with pore diameter of 0.1 µm and by 32% when using a membrane with 0.2 µm pore size. Electrode modification using porous membranes shifted the potential of electrochemical reduction and catalysis of cytochrome P450 3A4 in positive direction by 0.070-0.050 V, which indicates a thermodynamically more favorable process of electron transfer and enzymatic electrocatalysis.

Approaches for increasing the electrocatalitic efficiency of cytochrome P450 3A4

The electrochemically driven cytochrome P450 reactions have great promise as drug sensing device, new drug searching tool and bioreactor with broad synthetic application. In the present work, we proposed approaches for the increasing the efficiency of cytochrome P450 3A4 electrocatalysis, based on fine regulation and reproduction of nature hemeprotein catalytic cycle and electron transfer pathways on electrode. To analyze the comparative electrochemical and electrocatalytic activity, cytochrome P450 3A4 was immobilized on electrodes modified with a membrane-like synthetic surfactant, didodecyldimethylammonium bromide (DDAB). We used riboflavin, FMN and FAD as low molecular models of NADPH-dependent cytochrome P450 reductase for the improving and enhancement properties of catalytically responsible cytochrome P450 3A4-electrode. The efficiencies of electrocatalysis of erythromycin N-demethylation as well-known cytochrome P450 3A4 substrate in the case of riboflavin, FAD and FMN as electron transfer mediators were 135 ± 6, 171 ± 15 and 203 ± 10 %, respectively (in comparison with 100 ± 18 % erythromycin N-demethylation in the case of cytochrome P450 3A4-electrode as catalyst). Molecular modeling of cytochrome P450 3A4 complexes with riboflavin, FMN and FAD confirms possibility of binding isoalloxazine ring of riboflavin to the protein on the proximal side of hemeprotein, which is the place for binding of redox partners of the cytochrome P450.

Thermal Stability of Ionic Compounds on Nanostructured Metal Catalysts: Conversion of Quaternary Ammonium to Amines on Gold Nanoparticles

Quaternary ammonium halides are an important class of compounds because they are not only used as structural templates ororganic surface modifiers for inorganic minerals and other aluminosilicates such as zeolites, but are also well-known and widespread as phase-transfer catalysts and stabilizing agents for colloidal metal nanoparticle synthesis. Moreover, quaternary ammonium ions are frequently exploited as weakly coordinating cations in various ionic liquids. Thus, it is important to monitor, understand, and utilize thermal effects and limits of application. Herein, we report the thermal conversion of didodecyldimethylammonium bromide (DDAB) into organic amines on the surface of gold nanoparticles. In contrast to the pure compound, in which this decomposition appears as an endothermic process, the on-particle reaction is exothermic. This in situ modification of the ligand shell not only involves the essential step of halide removal through the gas phase but also turns out to be a valuable tool to produce uncovered metal sites and thus impacts the fabrication of nanostructured metal catalysts for ligand-directed chemistry.

Modified Peanut Shell as an Eco-Friendly Biosorbent for Effective Extraction of Triazole Fungicide Residues in Surface Water and Honey Samples before Their Determination by High-Performance Liquid Chromatography.

An eco-friendly sample preparation method that is based on the use of a modified peanut shell as an efficient biosorbent for the extraction of triazole residues before their analysis by high-performance liquid chromatography was reported. The four triazole fungicides were separated on a Purospher STAR RP-18 endcapped (4.6 × 150 mm, 5 μm) column with a mobile phase of 50% (v/v) acetonitrile at a flow rate of 1.0 mL min–1 and detection wavelength set at 220 nm. Peanut shells modified by didodecyldimethylammonium bromide were selected as an effective biosorbent material in the microextraction method. Scanning electron microscopy, transmission electron microscopy, and Fourier transform infrared spectroscopy were used to characterize the biosorbent. The effect of dominant parameters on the proposed microextraction method including the amount of sorbent, kind and concentration of surfactant, sodium hydroxide concentration, kind and amount of salt, sample volume, adsorption time, kind and volume desorption solvent, and desorption time was studied. Under the optimum condition, a good analytical performance for the proposed microextraction method was obtained with a wide linear range within the range of 9–1000 μg L–1, and low limits of detection (0.03 μg L–1 for all analytes) were obtained. Enrichment factors were achieved within the range of 30–51. The intra and interday precision values were evaluated in terms of percentage relative standard deviations (%RSD) and were less than 0.09 and 5.34% for the retention time and peak area, respectively. The proposed microextraction methods were used for extraction and analysis of triazole fungicides in water and honey samples. The recoveries in a satisfactory range of 70.0–118.8% were obtained.