Different colloidal particle formation process between conjugated polymer and unmodified C60 in preparation of suspension for electrophoretic deposition by reprecipitation method

Electrophoretic deposition provides material-efficient film formation on large area electrodes. In this study, it has been found that there is a significant difference in the colloidal particle formation process between a thiophene-based copolymer poly(3-octylthiophene- 2,5-diyl-co-3-decyloxythiophene-2,5-diyl) (POT-co-DOT) and C60 in preparation of suspension for electrophoretic deposition by reprecipitation method. This difference is attributed to the difference between low molecular weight materials with specific molecular weight and polymers with molecular weight distribution. The composition of POT-co-DOT:C60 composite film by electrophoretic deposition has also been estimated.

Quantitative analysis of non-equilibrium systems from short-time experimental data

Estimating entropy production directly from experimental trajectories is of great current interest but often requires a large amount of data or knowledge of the underlying dynamics. In this paper, we propose a minimal strategy using the short-time Thermodynamic Uncertainty Relation (TUR) by means of which we can simultaneously and quantitatively infer the thermodynamic force field acting on the system and the (potentially exact) rate of entropy production from experimental short-time trajectory data. We benchmark this scheme first for an experimental study of a colloidal particle system where exact analytical results are known, prior to studying the case of a colloidal particle in a hydrodynamical flow field, where neither analytical nor numerical results are available. In the latter case, we build an effective model of the system based on our results. In both cases, we also demonstrate that our results match with those obtained from another recently introduced scheme.

STUDY OF BETULIN STABILITY BY ELECTROKINETIC POTENTIAL DETERMINATION

Исследование стабильности бетулина методом определения электрокинетического потенциала. На сегодняшний день бетулин интересен в области медицины, косметики и пищевой промышленности, ведь он обладает огромным спектром биологических действий. Из него можно получить производные, которые, в свою очередь, имеют определенное хорошо выраженное действие и используются для производства различных медикаментов. И чтобы интенсифицировать процесс очистки и фильтрования бетулина для экономии времени и затрат на энергию, необходимо узнать его заряд коллоидной частицы и стабильность в водном растворе. Для этого было проведено определение электрокинетического потенциала. Найден ξ-потенциал бетулина в водном растворе, который показал, что с увеличением концентрации водного раствора бетулина вероятность разрушения дисперсии и возможность образования хлопьев при добавлении коагулянта или флогулянта повышаются. Определен заряд поверхности коллоидной частицы бетулина. Investigation of the stability of betulin by the method of determining the electrokinetic potential.Today betulin is interesting in the field of medicine, cosmetics and food industry, because it has a huge range of biological actions. From it, you can get derivatives, which in turn have a certain well-defined effect and are used for the production of various medicines. In order to intensify the process of cleaning and filtering betulin to save time and energy costs, we need to know its colloidal particle charge and stability in an aqueous solution. To do this, we conducted a method for determining the electrokinetic potential. we determined the zeta potential of betulin in an aqueous solution, which showed that with an increase in the concentration of betulin in water, the probability of destruction of the dispersion and the possibility of flocculation when adding a coagulant or flogulant increases. We determined the surface charge of a colloidal betulin particle.

Super-Resolution Imaging with Patchy Microspheres

The diffraction limit is a fundamental barrier in optical microscopy, which restricts the smallest resolvable feature size of a microscopic system. Microsphere-based microscopy has proven to be a promising tool for challenging the diffraction limit. Nevertheless, the microspheres have a low imaging contrast in air, which hinders the application of this technique. In this work, we demonstrate that this challenge can be effectively overcome by using partially Ag-plated microspheres. The deposited Ag film acts as an aperture stop that blocks a portion of the incident beam, forming a photonic hook and an oblique near-field illumination. Such a photonic hook significantly enhanced the imaging contrast of the system, as experimentally verified by imaging the Blu-ray disc surface and colloidal particle arrays.

Evaporation and deposition of inclined colloidal droplets

Colloidal droplets on flat solid substrates commonly leave symmetric ring-like deposits due to coffee-ring flows during evaporation. On inclined substrates, droplet shapes may become asymmetric by gravity. On this basis, it is not clear how their evaporation dynamics and final deposits are changed depending on inclination. Here we explore evaporation and deposition dynamics of colloidal droplets on inclined substrates, mainly by controlling colloidal particle size, substrate inclination, and relative humidity, which are crucial to gravitational intervention and evaporation dynamics. We experimentally investigate two different flows with opposite directions: downward sedimentation flows by gravity ($$v_s$$ v s ) and upward capillary flows by evaporation ($$v_c$$ v c ). We find that the competition of two flows determines the formation of final deposits with a flow speed ratio of $$\alpha = v_s/v_c$$ α = v s / v c . Notably, for $$\alpha$$ α $$\ll$$ ≪ 1, evaporation-driven upward flows overwhelm sedimentation-driven downward flows, resulting in accentuated particle movement towards the top ring, which seems to defy gravitational intervention. We suggest a possible explanation for the flow speed dependence of final deposits in evaporating colloidal droplets. This study offers a framework to understand the intervention of inclination to the formation of final deposits and how to overcome the deposit pattern radial asymmetry, achieving symmetric deposit widths from inclined colloidal droplets.

Precursor Linear Self-Assembly Nonhydrolytic Sol-Gel Synthesis of Ba0.7Sr0.3TiO3 Ceramic Fibers

Ba0.7Sr0.3TiO3 ceramic fibers were synthesized via the precursor linear self-assembly nonhydrolytic sol-gel (NHSG) method, taking TiCl4 as the titanium source, anhydrous barium acetate and strontium acetate as the barium source and strontium source, anhydrous ethanol and glycol as the oxygen donor and solvent, respectively. The NHSG method promotes the formation of Ba–O–Ti and Sr–O–Ti through heterogeneous condensation. The bimolecular association structure of the reaction intermediate (chlorotitanium ethoxide) between ethanol and titanium tetrachloride facilitates the self-linear assembly of precursors. It also enables linear colloidal particle formation and excellent spinnability of the sol. The novel Ba0.7Sr0.3TiO3 ceramic fibers would promote the flexibility of electronic products.