Evaporation-induced transport of a pure aqueous droplet by an aqueous mixture droplet

2020 ◽  
Vol 32 (3) ◽  
pp. 032003 ◽  
Author(s):  
B. Majhy ◽  
A. K. Sen
2015 ◽  
Vol 68 (8) ◽  
pp. 1293 ◽  
Author(s):  
Pakvipar Chaopanich ◽  
Punnama Siriphannon

Hydroxyapatite (HAp) nanoparticles were successfully synthesized from an aqueous mixture of Ca(NO3)2·4H2O and (NH4)2HPO4 by a facile single-step refluxing method using polystyrene sulfonate (PSS) as a template. The effects of reaction times, pH, and PSS concentration on the HAp formation were investigated. It was found that the crystalline HAp was obtained under all conditions after refluxing the precursors for 3 and 6 h. The longer refluxing time, the greater the crystallinity and the larger the crystallite size of the HAp nanoparticles. The HAp with poor crystallinity was obtained at pH 8.5; however, the well-crystallized HAp was obtained when reaction pH was increased to 9.5 and 10.5. In addition, the X-ray diffraction patterns revealed that the presence of PSS template caused the reduction of HAp crystallite size along the (002) plane from 52.6 nm of non-template HAp to 43.4 nm and 41.4 nm of HAp with 0.05 and 0.2 wt-% PSS template, respectively. Transmission electron microscopy images of the synthesized HAp revealed the rod-shaped crystals of all samples. The synthesized HAp nanoparticles were modified by l-aspartic acid (Asp) and l-arginine (Arg), having negative and positive charges, respectively. It was found that the zeta potential of HAp was significantly changed from +5.46 to –24.70 mV after modification with Asp, whereas it was +4.72 mV in the Arg-modified HAp. These results suggested that the negatively charged amino acid was preferentially adsorbed onto the synthesized HAp surface.


RSC Advances ◽  
2017 ◽  
Vol 7 (77) ◽  
pp. 48512-48525 ◽  
Author(s):  
Mohammad Mastiani ◽  
Babak Mosavati ◽  
Myeongsub (Mike) Kim

Two new flow regimes named unstable dripping and unstable jetting are identified in aqueous droplet generation within high inertial air flow inside a T-Junction microchannel.


2019 ◽  
Vol 15 (1) ◽  
pp. 82-87
Author(s):  
Alexandra Alexandrovna Kudrevatykh ◽  
Lyubov Stepanovna Klimenko ◽  
Timofey Petrovich Martyanov

Molecular interactions with various anions in the form of tetrabutylammonium salts in DMSO and DMSO-aqueous mixture were studied spectrophotometrically. It turned out that the solutions of 1-hydroxy-2-acylaminoanthraquinones in DMSO, originally yellow, became dark purple with the addition of cyanide, fluoride, phosphate, and acetate ions. The addition of other salts did not cause changes in the absorption spectra. When switching to aqueous DMSO, a contrasting color change in the solution was observed only with the addition of the cyanide ion. The stability constants of the complexes and the metrological characteristics of the processes were determined. On the basis of 1hydroxy-2-benzoylaminoanthraquinone, colorimetric test strips were made and tested for the detection of CN-ions in an aqueous medium.


2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Ruaa Mohamed Akode ◽  
Shaza Wagiealla Shantier ◽  
Elrasheed Ahmed Gadkariem ◽  
Magdi Awadalla Mohamed

This work presents UV first derivative spectrophotometry as a precise, accurate, and feasible method for simultaneous determination of diminazene diaceturate and phenazone in bulk and dosage forms. The absorbance values of diminazene diaceturate and phenazone aqueous mixture were obtained at 398 nm and 273 nm, respectively. The developed method was proved to be linear over the concentration ranges (2–10) μg/mL and (2.496–12.48) μg/mL for diminazene diaceturate and phenazone, respectively, with good correlation coefficients (not less than 0.997). The detection and quantitation limits were found to be (LOD = 0.63 and 0.48 μg/mL; LOQ = 1.92 and 1.47 μg/mL, resp.). The developed method was employed for stability studies of both drugs under different stress conditions. Diminazene diaceturate was prone to degrade at acidic pH via first-order kinetics. The degradation process was found to be temperature dependent with an activation energy of 7.48 kcal/mole. Photo-stability was also investigated for this drug.


2011 ◽  
Vol 89 (12) ◽  
pp. 1506-1511 ◽  
Author(s):  
Jenkins Yin Ki Tsang ◽  
Kin Shing Chan

A synthetic route for iridium porphyrin amido complexes has been established. Treatment of a THF solution of Ir(ttp)(CO)Cl (1) (ttp = 5,10,15,20-tetrakis(p-tolyl)porphyrinato dianion) with an aqueous mixture of NaOH and NaBH4, followed by 2-iodoethanol leads to the clean formation of the β-hydroxyethyl complex Ir(ttp)(C2H4OH) (2) in 92% yield. Heating a pyridine solution of complex 2 in the presence of ca. 5–10 equiv. of phthalimide (HNC8H4O2; HPhth) leads to the formation of Ir(ttp)(C5H5N)(CH2CH2Phth) (3). The replacement of pyridine by THF as the reaction solvent leads to the formation of the THF adduct Ir(ttp)(THF)(Phth) (4), which has been characterized spectroscopically. Heating a solution of 4 in pyridine leads to the formation of Ir(ttp)(C5H5N)(Phth) (5), which has been isolated in 72% yield. Complexes 3 and 5 have been characterized by X-ray crystallographic studies. Complexes 4 and 5 are rare examples of monomeric late transition metal-amido complexes and are the first examples of iridium-amido complexes featuring a porphyrin as a supporting ligand.


2018 ◽  
Vol 25 (35) ◽  
pp. 34968-34975 ◽  
Author(s):  
Magdalena Foszpańczyk ◽  
Emilia Drozdek ◽  
Marta Gmurek ◽  
Stanisław Ledakowicz

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