Encapsulating functionalized graphene quantum dot into metal-organic framework as a ratiometric fluorescent nanoprobe for doxycycline sensing.

A distinctive fluorescent nanoprobe with the function of doxycycline identification was designed by encapsulating histidine and serine-functionalized graphene quantum dots (His-GQDs-Ser) into the luminescent metal-organic frameworks (MOF). The synthesized nanoprobe displayed the merits of prominent selectivity, wide detection range, and high sensitivity. The interaction of doxycycline and the fabricated fluorescent nanoprobe contributed to the phenomenon of the suppression of the fluorescence of the His-GQDs-Ser and enhancement of the MOF fluorescence. Linear relation between the concentration of doxycycline and the ratio fluorescence intensity of the nanoprobe was observed, which evidenced the brilliant capability in the ranges 0.003-6.25 µM and 6.25-25 µM with a detection limit of 1.8 nM. Additionally, the practicability of the probe was verified in analysis of spiked milk sample, and the satisfactory recoveries of doxycycline varied from 97.39 to 103.61%, with relative standard deviations in the range 0.62-1.42%. A proportional fluorescence sensor for doxycycline detection in standard solution was constructed, which provides a potential for the development of other fluorescence detection systems.

Highly photoluminescent nitrogen-doped carbon quantum dots as a green fluorescence probe for determination of myricetin.

Highly photoluminescent N-doped carbon quantum dots (N-CDs) which the quantum yield reached 63% were prepared through hydrothermal treatment. The obtained N-CDs displayed a uniform distribution of particle size, superior stability in high-salt conditions, and excellent sensitivity. A green fluorescence probe based on N-CDs was constructed for ultrasensitive determination of myricetin in vine tea on account of the static quenching. The N-CDs presented excellent linear fluorescence response in the concentration range of 0.2-40 µM and 56-112 µM and with a low detection limit of 56 nM. Additionally, the practicability of the probe was verified in spiked vine tea sample, and the satisfactory recoveries of myricetin varied from 98.8% to 101.2%, with relative standard deviations in the range of 1.52%-3.48%. It is the first time to employ N-CDs without any material modification as a fluorescence sensor to detect myricetin, which is a promising approach to expand the path for myricetin screening.

Diblock, Triblock and Cyclic Amphiphilic Copolymers with CO2 Switchability: Effects of Topology.

The combination of topology and CO2 switchability could provide new options for amphiphilic copolymers. Cyclic molecules supply novel topologies, and CO2 switching provides stimulus responsiveness. Cyclic poly(2-(diethylamino)ethyl methacrylate)-b-poly(ethylene oxide) and their corresponding block copolymers were prepared from poly(ethylene oxide) and 2-(diethylamino)ethyl methacrylate via atom transfer radical polymerization and Keck allylation with a Hoveyda-Grubbs catalyst. Changes in conductivity, surface activity, and hydrodynamic size were examined to illustrate the switchability of the produced amphiphilic copolymers upon contact with CO2 in the presence of water. The reversible emulsification and switchable viscosity behaviors of the copolymers were also demonstrated.

Cryogenic viscoelastic surfactant fluids: Fabrication and application in a subzero environment.

HYPOTHESIS: Current viscoelastic surfactant (VES) aqueous solutions quickly freeze and thus, lose their viscoelasticity and flowability at subzero temperatures, limiting their practical use in cold environments. Therefore, it is highly desirable to develop cryo-VES fluids with freezing point far below 0 °C. Since addition of alcohol antifreeze greatly reduces the freezing point of water, cryo-VES fluids might be generated in the presence of alcohols. EXPERIMENTS: The self-assembly behavior of a C22-tailed surfactant, erucyl dimethyl amidopropyl betaine (EDAB), in eight alcohol/water cosolvents from 20 to -20 °C was studied by pyrene fluorescent probe, cryo-TEM imaging and cryo-SNAS characterization, and the solution properties of the mixtures were investigated by rheological test. FINDINGS: It is found that the alcohol molecular structure, content and temperature play crucial roles dominating EDAB self-assembly behavior. Monohydric alcohols are unfavorable for micelles formation and growth, thus VES fluids cannot be obtained in the presence of 50 vol% monohydric alcohols even at subfreezing temperatures. On the contrary, dihydric and trihydric alcohols with short alkyl chain show less negative effect on EDAB micellization. Thus, cryo-VES fluids can be formed in the presence of 50 vol% ethylene glycol, 1,3-propanediol or glycerol due to the formation of wormlike micelles. These cryo-VES fluids with different alcohols exhibit different temperature-sensitivity and rheological properties, furnishing them with potential applications in anti-freeze hydraulic fracking fluids and aircraft deicing/anti-icing fluids.

Correction: Cryogenic wormlike micelles.

Correction for 'Cryogenic wormlike micelles' by Hongyao Yin et al., Soft Matter, 2019, 15, 2511-2516.

Cryogenic wormlike micelles.

Cryogenic wormlike micellar solutions which possess a freezing point far below 0 °C while retaining rheological properties similar to those of ordinary wormlike micellar solutions are fabricated from the self-assembly of a C22-tailed monounsaturated zwitterionic surfactant, erucyl dimethyl amidopropyl betaine, in an ethylene glycol/water co-solvent at subzero temperature. Such fluids may find potential applications in fields where viscoelasticity is highly desired at subfreezing temperatures.

Thermally induced structural transitions from fluids to hydrogels with pH-switchable anionic wormlike micelles.

A novel pH-switchable anionic wormlike micellar system has been developed by simply changing pH value of natural erucic acid solutions without needing specialized organic synthesis or addition of hydrotropes. Through rheology, optical transmittance, and cryo-TEM observation, it was found that at 60 °C, the 100 mM erucic acid solutions transform from low viscous emulsion-like fluids to viscoelastic hydrogels when the pH is increased from 8.03 to 12.35, and when the pH is cycled between 9.02 and 12.35, the viscosity of the solutions varies correspondingly between 2 and 200,000 mPas, five orders of magnitude in viscosity range. Such a reversible switch can be easily cycled more than four times without any deterioration. In addition, when the pH is fixed between 9.0 and 12.35, the solutions shift to highly elastic solid-like gels with decreasing temperature. These pH-switchable and temperature-sensitive rheological properties are attributed to the presence of carboxylic groups in the erucic acid molecules. With increasing pH, erucic acid is converted into an anionic surfactant, sodium erucate, which self-assembles into aggregates evolving from spherical micelles to wormlike micelles; when temperature is decreased, these disordered micellar structures become highly ordered under the effect of crystallization of hydrophobic erucate chains, forming opaque solid-like hydrogels.

Wormlike micelles formed by sodium erucate in the presence of a tetraalkylammonium hydrotrope.

Anionic wormlike micelles, particularly those formed by long-chain carboxylate surfactants, are relatively less documented though their cationic or zwitterionic counterparts are frequently reported. In this study, the wormlike micelles of sodium erucate (NaOEr), a C22-tailed anionic surfactant with a monounsaturated tail, in the presence of a tetraalkylammonium hydrotrope were investigated for the first time. The different effects of two hydrotropes, benzyl trimethyl ammonium bromide (BTAB) and tetramethyl ammonium bromide (TMAB), on the phase behavior and rheological behaviors were compared, and the influences of surfactant concentration and temperature on the rheological properties of NaOEr solutions were also examined. Both organic salts can lower the Krafft temperature of NaOEr solutions and thus improve its water solubility, but BTAB can make T(K) drop more sharply. At a fixed NaOEr concentration, less BTAB is demanded to induce the formation of viscoelastic solution and to obtain the maximum viscosity of NaOEr solution; at a constant salt concentration, with increasing NaOEr content, the NaOEr-BTAB system shows a larger zero-shear viscosity (η(0)), relaxation time, and plateau modulus but lower overlapping concentration than those of the NaOEr-TMAB system. The occurrence of maximum η(0) with increasing salt content for the NaOEr-BTAB system results from the formation of vesicles and L(3) phases, which were verified by cryo-TEM observations. η(0) shows an exponential decrease with increasing temperature; nevertheless it still remains above 10(3) mPa·s even at 90 °C.

Wormlike micelles and solution properties of a C22-tailed amidosulfobetaine surfactant.

Wormlike micelles have been observed and explained in a wide variety of different types of surfactants except sulfobetaine ones. Here, we first report branched worms formed by a C22-tailed amidosulfobetaine surfactant-3-(N-erucamidopropyl-N,N-dimethyl ammonium) propane sulfonate (EDAS). Increasing EDAS concentration in the semidilute region increases the viscosity by several orders of magnitude and forms viscoelastic micellar solution of entangled and branched worms. The intermicellar branching is proved by rheological methods and Cryo-TEM observation. Besides, the rheological experiments indicate that EDAS worms show some advantages such as low overlapping concentration, insensitive to inorganic salt, stable over the whole pH range.