DETECTION METHOD OF WORMLIKE MICELLES

Abstract

The present disclosure provides a detection method of wormlike micelles, and belongs to the technical field of analytical chemistry. In the present disclosure, z-ArN.sub.2.sup.+ is used as a chemical probe substance; a long-chain probe is added to a test solution for probing an interfacial region, and a short-chain probe is added to a surfactant-free control solution. A selectivity of the probe with different nucleophiles is determined by the above method, and a yield of an obtained product is measured by high-performance liquid chromatography (HPLC); and the wormlike micelles are detected by measuring the yield of the product using the selectivity of the short-chain probe to be converted into an interfacial mole number. The wormlike micelles are detected by chemical probes, and the chemical probes have a simple preparation method, a low cost, real-time detection, and broad prospects for use.

Claims

1. A detection method of wormlike micelles, wherein the detection method is implemented by a z-ArN.sub.2.sup.+ long-chain probe and a z-ArN.sub.2.sup.+ short-chain probe, and the z-ArN.sub.2.sup.+ has a structure shown in Formula I: ##STR00003## in the z-ArN.sub.2.sup.+ short-chain probe, z=1, and R is —CH.sub.3; and in the z-ArN.sub.2.sup.+ long-chain probe, z=16, and R is —C.sub.16H.sub.33.

2. The detection method of wormlike micelles according to claim 1, comprising the following steps: (1) preparing the long-chain probe into an acetonitrile stock solution with a concentration of 0.005 M to 0.05 M, and preparing the short-chain probe into an acetonitrile stock solution with a concentration of 0.05 M to 0.5 M; (2) adding a surfactant to a volumetric flask, dissolving and diluting with a diluent, and adding the stock solution of the long-chain probe obtained in step (1) to obtain a test solution; wherein the test solution has 5×10.sup.−4 M to 5×10.sup.−5 M of the long-chain probe and 1×10.sup.−3 M to 2 M of the surfactant by concentration; (3) replacing the surfactant in step (2) with an ammonium salt or a sulfonate, dissolving and diluting with the diluent, and adding the stock solution of the short-chain probe obtained in step (1) to obtain a control solution; wherein the control solution has 5×10.sup.−3 M to 5×10.sup.−4 M of the short-chain probe by concentration; (4) conducting a reaction on the test solution obtained in step (2) at 25° C. to 60° C. for 5 h to 48 h under sealing in the dark, diluting an obtained reaction product with the diluent, and measuring a yield of the product by high-performance liquid chromatography (HPLC); (5) repeating the operations of step (4) on the control solution obtained in step (3); and (6) obtaining the yield of the product measured by the HPLC from an average of peak areas of three or more repeated injections and calibration curves of cetyldimethylphenol and cetyldimethylbromobenzene.

3. The detection method of wormlike micelles according to claim 2, wherein in step (2), the surfactant is cetyltrimethylammonium bromide (CTAB).

4. The detection method of wormlike micelles according to claim 2, wherein in steps (2) to (4), the diluent is at least one selected from the group consisting of methanol, acetonitrile, and water.

5. The detection method of wormlike micelles according to claim 2, wherein in step (3), the ammonium salt is at least one selected from the group consisting of tetramethylammonium salt and tetraethylammonium salt, and the sulfonate is methylsulfonate.

6. The detection method of wormlike micelles according to claim 2, wherein the HPLC is conducted by a C18 chromatographic column with a length of 25 cm and using 65% methanol: 35% isopropanol (v/v) as a mobile phase at a flow rate of 0.4 mL/min, a λ of 220 nm, and an injection volume of 100 μL.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0023] FIG. 1 shows a variation trend of a zero shear viscosity of a colloidal solution along with an alcohol concentration in Example 1 of the present disclosure;

[0024] FIG. 2 shows a variation curve of an elastic modulus G′ and a viscous modulus G″ of the colloidal solution along with an oscillation frequency when alcohol systems are different in Example 1 of the present disclosure; and

[0025] FIG. 3 shows a variation trend of alcohol, water, and bromide ion concentrations along with the alcohol concentration in a micelle interface region in Example 1 of the present disclosure.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0026] The present disclosure is further described below with reference to examples. In the following examples, the experimental methods or test methods, unless otherwise specified, are conventional methods; the raw materials and auxiliary agents, unless otherwise specified, are obtained from conventional commercial channels, or prepared by conventional methods.

Example 1

[0027] (1) A long-chain probe 16-ArN.sub.2BF.sub.4 was prepared into a stock solution with a concentration of 0.01 M, and placed in acetonitrile for later use; 2 ml of a 0.1 M CTAB/0.05 M KBr/5 mM to 300 mM cinnamyl alcohol system was prepared for later use; 20 □μL of the long-chain probe 16-ArN.sub.2BF.sub.4 stock solution ice-encapsulated in the acetonitrile was added to 2 L of the 0.1 M CTAB/0.05 M KBr/5 mM to 300 mM cinnamyl alcohol system, to obtain a solution with a concentration of 1.2×10.sup.−5 M to 2×10.sup.−4 M; the above solution was mixed well, placed in a dark and sealed environment, and reacted at 25° C. for 48 h; a reaction product was diluted with methanol, and then measured by HPLC. The HPLC was conducted by a C18 chromatographic column with a length of 25 cm and using 65% methanol: 35% isopropanol (v/v) as a mobile phase at a flow rate of 0.4 mL/min, a λ of 220 nm, and an injection volume of 100 μL.

[0028] The yield of the product was obtained from an average of peak areas of three or more repeated injections and calibration curves of cetyldimethylphenol and cetyldimethylbromobenzene.

[0029] (2) The long-chain probe 16-ArN.sub.2BF.sub.4 in step (1) was replaced with a short-chain probe 1-ArN.sub.2BF.sub.4, and the 0.1 M CTAB/0.05 M KBr/5 mM to 300 mM cinnamyl alcohol system in step (1) was replaced with an aqueous methanol system of 0.01 M to 3 M tetramethylammonium bromide (TMAB), and other operations were the same as those in step (1).

Example 2

[0030] The cinnamyl alcohol in Example 1 was replaced with benzyl alcohol, and other operations were the same as those in Example 1.

Example 3

[0031] The cinnamyl alcohol in Example 1 was replaced with phenethyl alcohol, and other operations were the same as those in Example 1.

Example 4

[0032] The cinnamyl alcohol in Example 1 was replaced with anisyl alcohol, and other operations were the same as those in Example 1.

[0033] In the 0.1 M CTAB/0.05 M KBr/5 mM to 300 mM cinnamyl alcohol system, it was seen from rheology that in the cinnamyl alcohol system, wormlike micelles were formed in a region where a cinnamyl alcohol concentration was about 50 mM, while no wormlike micelles were formed in the systems of phenethyl alcohol, benzyl alcohol, and anisyl alcohol, and the results were shown in FIG. 1.

[0034] It was further proved that the cinnamyl alcohol induced transformation of ellipsoid micelles to wormlike micelles in the system. The changes of elastic moduli G′ and viscous moduli G″ of the 0.1 M CTAB/0.05 M KBr/5 mM to 300 mM perfume alcohol systems at 25° C. were separately investigated along with oscillation frequency. As shown in FIG. 2, the system with wormlike micelles had the viscous modulus G″ greater than the elastic modulus G′ in the low-frequency region, and the viscous modulus G″ less than the elastic modulus G′ in the high-frequency region. That is, there was intersection of the curves of G″ and G′ as a sign of the formation of wormlike micelles. The concentrations of perfume alcohols each were corresponding to a highest point of η.sub.0 value of each alcohol in FIG. 1, where cinnamyl alcohol was 55 mM, and phenylethyl alcohol, benzyl alcohol, and anisyl alcohol each were 40 mM. It was seen from FIG. 2 that after adding 40 mM of the phenethyl alcohol, 40 mM of the benzyl alcohol, and 40 mM of the anisyl alcohol, the system always exhibited viscosity, showing that the systems with phenethyl alcohol, benzyl alcohol, and anisyl alcohol had no formation of wormlike micelles. However, a dynamic rheological effect of the cinnamyl alcohol showed viscosity at low frequency and elasticity at high frequency, indicating existence of the wormlike micelles.

[0035] The chemical compositions of the micelle interface regions in the above four 0.1 M CTAB/0.05 M KBr/5 mM to 300 mM perfume alcohol systems were detected by chemical probes. The results were shown in FIG. 3. An alcohol concentration was significantly increased at the interface of the cinnamyl alcohol system with wormlike micelles, while changes in the alcohol concentration each were small at interfaces of the other three alcohol systems; meanwhile, a water concentration decreased at the interface of the cinnamyl alcohol system with wormlike micelles, while water concentrations each increased slightly at the interfaces of the other three alcohol systems.

[0036] The above descriptions are merely preferred implementations of the present disclosure. It should be noted that a person of ordinary skill in the art may further make several improvements and modifications without departing from the principle of the present disclosure, but such improvements and modifications should be deemed as falling within the protection scope of the present disclosure.