Effect of Process Variable on the Gelation Time of Sulfonated Polyacrylamide Nanocomposite Hydrogel

Among the methods available to reduce water production during oil recovery, injecting a gelling system composed of a polymer and a crosslinker has been widely used. In this study, a Plackett-Burman design was used for screening a large number of factors such as concentrations of polymer, crosslinker, pH, temperature, and presence or absence of NaCl, CaCl₂, MgCl₂, KCl, thiourea, sodium lactate, and nanoclay on the gelation time of sulfonated polyacrylamide nanocomposite hydrogels by rheological tests. Among these factors, temperature, pH, and CaCl₂ concentration were found to have the greatest effect on the gelation time. The effects of these three factors and their interactions on the gelation time were then determined by using central composite design of response surface method. As a result, the interactions of CaCl₂ concentration with temperature and pH were considerably more than the interactions of pH and temperature on the gelation time. At low pH (3 < pH < 7), the gelation time decreased by decrease of pH while at CaCl₂ concentration of 3750–11250 ppm and at 7 < pH < 11, the gelation time increased with the increase of pH. It was found that temperature was the most effective parameter to control the gelation time.     

Preparation of a solid-state ion-selective electrode based on polypyrrole conducting polymer for magnesium ion

In this study, a potentiometric sensor based on a pencil graphite electrode (PGE) coated with polypyrrole doped with Titan yellow dye (PPy/TY) was prepared for potentiometric determination of magnesium ion in aqueous solutions. The structural characteristics of magnesium sensor electrode (PGE/PPy/TYMg) were studied using scanning electron microscopy and Fourier transform infrared along with energy-dispersive spectroscopy. Under the optimal conditions, the electrode reveals a good Nernstian behavior with slope of 28.27 ± 0.40 mV per decade over the concentration range of 1.0 × 10^?5–5.0 × 10^?2 M and a detection limit of 6.28 × 10^?6 M. The potentiometric response of fabricated electrode toward magnesium ion was found to be independent of the pH of the test solution in the pH range of 4.5–8.0. The electrode showed fast response time (<10 s) and good shelf lifetime (>2 months). The prepared magnesium sensor electrode can also be used as an indicator electrode in potentiometric titration of Mg²⁺ with EDTA with distinguished end point. The electrode revealed good selectivity with respect to many cations including alkali, alkaline earth, transition and heavy metal ions. The introduced magnesium electrode was used for measurement of Mg²⁺ ion in real samples without any serious interferences from other ions.     

Introducing Organic Gas Steam-Liquid Extraction as a New Preconcentration Method for Benzene,Toluene, Ethylbenzene and Xylene Determination in Water Samples by Gas Chromatography-Flame Ionization Detection

Journal of Analytical Chemistry - In this study, for the first time, the organic gas steam-liquid extraction by a special hand-made cell was used as a simple and inexpensive preconcentration...     

Energy,exergy, and sensitivity analyses of a new integrated system for generation of liquid methanol,liquefied natural gas,and crude helium using organic Rankine cycle,and solar collectors

Journal of Thermal Analysis and Calorimetry - The increasing growth of helium consumption in industries and the limited resources of this element are the challenges that industries will face in the...     

A renewable approach to capture CO2 in Iran: thermodynamic and exergy analyses

Journal of Thermal Analysis and Calorimetry - This work presents numerical simulation of two-dimensional thermogravitational energy transport in a chamber filled with copper–water ( $${\hbox...     

Polyethylene Glycol Functionalized Graphene Oxide Nanoparticles Loaded with Nigella sativa Extract: A Smart Antibacterial Therapeutic Drug Delivery System

Flaky graphene oxide (GO) nanoparticles (NPs) were synthesized using Hummer’s method and then capped with polyethylene glycol (PEG) by an esterification reaction, then loaded with Nigella sativa (N. sativa) seed extract. Aiming to investigate their potential use as a smart drug delivery system against Staphylococcus aureus and Escherichia coli, the spectral and structural characteristics of GO-PEG NPs were comprehensively analyzed by XRD, AFM, TEM, FTIR, and UV- Vis. XRD patterns revealed that GO-PEG had different crystalline structures and defects, as well as a higher interlayer spacing. AFM results showed GONPs with the main grain size of 24.41 nm, while GONPs–PEG revealed graphene oxide aggregation with the main grain size of 287.04 nm after loading N. sativa seed extract, which was verified by TEM examination. A strong OH bond appeared in FTIR spectra. Furthermore, UV- Vis absorbance peaks at (275, 284, 324, and 327) nm seemed to be correlated with GONPs, GO–PEG, N. sativa seed extract, and GO –PEG- N. sativa extract. The drug delivery system was observed to destroy the bacteria by permeating the bacterial nucleic acid and cytoplasmic membrane, resulting in the loss of cell wall integrity, nucleic acid damage, and increased cell-wall permeability.     

含吡啶的大环席夫碱锰(Ⅱ)配合物:合成、表征及抗菌性质(英文)

在Mn髤模板作用下,2,6-diacetylpyridine(DAP)及合适链状胺化合物通过[1+1]环缩合反应,合成了3个大环席夫碱配合物,并进行了红外、元素分析、质谱及电导率等表征及研究。测得了配合物[MnL1(CH3CN)](ClO4)2的晶体结构,中心离子呈现出稍微扭曲的五角锥配位构型。研究了配合物对S.aureus(ATCC 6633),B.cereus(ATCC 7064),C.xerosis(ATCC 373)(gram-positive bacterial strains),E.coli(PTCC 10009),K.pneuomoniae(MTCC 109),and P.vulgaris(lio)(gram-negative bacterial strains)的抗菌活性。结果显示[MnL3](ClO4)2抗菌活性明显优于[MnL1(CH3CN)](ClO4)2and[MnL2](ClO4)2。在25℃条件下0.1 mol·L-1 KCl溶液中,通过电位计量法测定了化合物的质子化常数。     

聚(4-乙烯基吡啶)硫酸氢盐: 一个新的高效催化剂用于无溶剂条件下合成13-芳香基-茚并 [1,2-b] 石脑油 [1,2-e] 吡喃-12(13H)-酮（英文）

An facile and efficient protocol for the synthesis of 13‐aryl‐indeno[1,2‐b]naphtha[1,2‐e]pyran‐ 12(13H)‐ ones has been developed that proceeds via the one‐pot three‐component sequential reaction of an aromatic aldehyde with β‐naphthol and 2H‐indene‐1,3‐dione under solvent‐free conditions in the presence of a poly(4‐vinylpyridinium)hydrogen sulfate(P(4‐VPH)HSO4) catalyst. The catalyst can be reused several times, making this procedure facile, practical, and sustainable. The simple experimental procedure, solvent‐free reaction conditions, use of an inexpensive catalyst, short react time, and excellent yields are some of the major advantages of this methodology.     

Controllable one-step synthesis of ZnO nanostructures using molybdophosphoric acid

ZnO nanostructures were synthesised in a hydrothermal reaction of zinc acetate in the presence of molybdophosphoric acid (H₃[PMo₁₂O₄₀]) as well as its vanadium-substituted acid (H₄[PMo₁₁VO₄₀]) at various times, temperatures, and concentrations. The ZnO nanostructures were characterised by X-ray diffraction, transmission electron microscopy, and Fourier transform infrared spectroscopy. The results demonstrated that the synthesised products are crystalline with a zincite hexagonal phase. Various ZnO nanostructures, such as nanoparticles, microrods, and nanosheets, were produced by changing the experimental conditions. The photocatalytic degradation of methyl orange was also investigated using the ZnO nanoparticles thus prepared. These particles exhibited high performance in the photocatalytic degradation of MO and almost 100 % decolourisation occurred within only 20 min.     

An eco-friendly catalytic route for one-pot synthesis of 2-amino-6-(2-oxo-2Hchromen-3-yl)-4-arylnicotinonitrile derivatives by silica-supported perchloric acid (HClO4–SiO2) under solvent-free conditions

A facile and environmentally benign synthesis of some 2-amino-6-(2-oxo-2H-chromen-3-yl)-4-arylnicotinonitrile derivatives from the reaction of 3-acetylcoumarin, aromatic aldehydes, and malononitrile under solvent-free condition in the presence of silica-supported perchloric acid (HClO₄–SiO₂) is described. The ability to reuse the catalyst, the high yields, and ease of purification are the important features of this process.