Introduction of amino groups into acid-resistant MOFs for enhanced U(vi) sorption

2015 ◽  
Vol 3 (2) ◽  
pp. 525-534 ◽  
Author(s):  
Zhi-Qiang Bai ◽  
Li-Yong Yuan ◽  
Lin Zhu ◽  
Zhi-Rong Liu ◽  
Sheng-Qi Chu ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Amino Group ◽  
Amino Groups ◽  
Amine Grafting

Amine grafting on MOFs greatly enhances the adsorbability of Cr-MIL-101 towards U(vi) from an aqueous solution, and the enhancement depends on the coverage and flexibility of the grafted amino group.

Investigation of the effect of ring size on the product distribution for the Schiff base reaction of 2-acetylcycloalkanones with diamino alkanes

1995 ◽  
Vol 73 (1) ◽  
pp. 16-21 ◽  
Author(s):  
Raul G. Enriquez ◽  
Juan M. Fernandez-G ◽  
Ismael Leon ◽  
William F. Reynolds ◽  
Ji.-Ping Yang ◽  
...  
Keyword(s):  
Schiff Base ◽  
Condensation Reaction ◽  
2D Nmr ◽  
Product Distribution ◽  
Major Product ◽  
Ring Size ◽  
Amino Group ◽  
Amino Groups ◽  
Similar Product ◽  
Acetyl Group

The Schiff base condensation reaction of 1,2-diaminoethane with a series of 2-acetylcycloalkanones (from cyclopentanone to cyclooctanone) has been investigated and the products characterized by two-dimensional nuclear magnetic resonance. The site of attack of the amino groups, i.e., ring ketone or acetyl ketone, is determined primarily by ring size. 2-Acetylcyclohexanone yields two products in ca. 9:1 ratio, the major product where the two amino groups attack at the ring ketones of two different cyclohexanone molecules, and the minor product where one amino group attacks one ring carbonyl of one cyclohexanone while the second amino group attacks the acetyl group of another. 2-Acetylcyclopentanone yields all three possible products with the major product involving attack at the acetyl groups of two different cyclopentanones. The corresponding reactions for 2-acetylcycloheptanone and 2-acetylcyclooctanone each give a single product corresponding to attack at the acetyl groups of two different cycloalkanones. Similar product distributions are observed for the reactions of the different 2-acetylcycloalkanones with 1,4-diaminobutane. Keywords: Schiff base reactions, diketones, 2D NMR.

scholarly journals Removal of Organic Compounds with an Amino Group during the Nanofiltration Process

Membranes ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 58
Author(s):  
Renata Żyłła ◽  
Magdalena Foszpańczyk ◽  
Magdalena Olak-Kucharczyk ◽  
Joanna Marszałek ◽  
Stanisław Ledakowicz
Keyword(s):  
Organic Compounds ◽  
Natural Organic Matter ◽  
Oxidation Product ◽  
Membrane Filtration ◽  
Separation Efficiency ◽  
Ph Value ◽  
Oxidation Products ◽  
Low Molecular Weight ◽  
Amino Group ◽  
Amino Groups

The research covered the process of nanofiltration of low molecular weight organic compounds in aqueous solution. The article presents the results of experiments on membrane filtration of compounds containing amino groups in the aromatic ring and comparing them with the results for compounds without amino groups. The research was carried out for several commercial polymer membranes: HL, TS40, TS80, DL from various manufacturers. It has been shown that the presence of the amino group and its position in relation to the carboxyl group in the molecule affects the retention in the nanofiltration process. The research also included the oxidation products of selected pharmaceuticals. It has been shown that 4-Amino-3,5-dichlorophenol—a oxidation product of diclofenac and 4-ethylbenzaldehyde—a oxidation product of IBU, show poor separation efficiency on the selected commercial membranes, regardless of the pH value and the presence of natural organic matter (NOM). It has been shown that pre-ozonation of natural river water can improve the retention of pollutants removed.

scholarly journals Adsorption of Phenol from Aqueous Solution by Aminated Hypercrosslinked Polymers

2005 ◽  
Vol 23 (4) ◽  
pp. 335-346 ◽  
Author(s):  
Yue Sun ◽  
Jin-Long Chen ◽  
Ai-Min Li ◽  
Fu-Qiang Liu ◽  
Quan-Xing Zhang
Keyword(s):  
Aqueous Solution ◽  
Adsorption Process ◽  
Kinetic Studies ◽  
Amino Group ◽  
Commercial Resin ◽  
The Matrix ◽  
Basic Anion Exchange Resin ◽  
Tertiary Amino ◽  
Basic Anion ◽  
Hypercrosslinked Polymeric Adsorbent

The adsorption of phenol from aqueous solution onto the hypercrosslinked polymeric adsorbent NDA-100 and its dimethylamine aminated derivatives AH-1, AH-2 and AH-3, the commercial resin Amberlite XAD-4 and the weakly basic anion-exchange resin D301 was compared. Of the tested polymers, the aminated hypercrosslinked resins had the highest adsorption capacities. The empirical Freundlich equation was successfully employed to describe the adsorption process. The specific surface area and the micropore structure of the adsorbent together with the tertiary amino group on the matrix affected the adsorption performance towards phenol. Furthermore, these factors also influenced the thermodynamic properties. Kinetic studies demonstrated that the presence of the tertiary amino group on the polymer matrix decreased the adsorption rate and increased the apparent activation energy of the adsorption process.

Effect of amino group protonation on the carboxyl group in aqueous glycine observed by O 1s X-ray emission spectroscopy

2018 ◽  
Vol 20 (36) ◽  
pp. 23214-23221 ◽  
Author(s):  
Y. Horikawa ◽  
T. Tokushima ◽  
O. Takahashi ◽  
Y. Harada ◽  
A. Hiraya ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Amino Acid ◽  
Electronic Structures ◽  
Emission Spectroscopy ◽  
Selective Excitation ◽  
Carboxyl Group ◽  
Amino Group ◽  
X Ray ◽  
Excitation Conditions ◽  
Amino Acid Glycine

The valence electronic structures of the amino acid glycine in aqueous solution were investigated in detail through X-ray emission spectroscopy at O 1s excitation under selective excitation conditions of the CO site in the carboxyl group.

Rate of lactamization of benzylstrychnine in acid solution

1984 ◽  
Vol 62 (1) ◽  
pp. 144-146 ◽  
Author(s):  
John T. Edward ◽  
Sin Cheong Wong ◽  
Robert A. McClelland
Keyword(s):  
Aqueous Solution ◽  
Sulfuric Acid ◽  
Acid Solution ◽  
Acid Concentration ◽  
Amino Group ◽  
Cage Structure ◽  
Basic Formula

The rate of lactamization of benzylstrychnine in aqueous solution at 25 °C increases with acid concentration up to 5–10% sulfuric acid, and thereafter decreases. The maximum can be explained by taking account of the extent of protonation of the aromatic amino group with increasing acid concentration. This amino group is unusually weakly basic [Formula: see text], perhaps because it is locked in an extremely rigid cage structure which opposes the rehybridization of N which must take place when it is protonated.

Condensation de la poly-L-lysine et de la poly- L-ornithine avec des dérivés de bases puriques et de sulfamides

1969 ◽  
Vol 47 (19) ◽  
pp. 3641-3646 ◽  
Author(s):  
Louis Berlinguet ◽  
Jacky Gautier
Keyword(s):  
Aqueous Solution ◽  
Amino Acids ◽  
Free Amino ◽  
Sulfonyl Chloride ◽  
Amino Groups ◽  
Carbodiimide Method

Free ε-amino groups of poly-L-lysine and poly-L-ornithine were alkylated in aqueous solution with 6-chloropurine and 6-chloropurine-riboside, were acylated with 4-acetylamino benzene sulfonyl chloride, and were condensed with N-(4-acetylamino benzene sulfonyl)-glycine using carbodiimide method. Approximately 50% of the free amino groups of the basic polypetides were substituted. The same method was used to prepare poly-α-amino acids bearing radioactive substituants.

Anomalous phase behavior in blends of -SO3H terminated polystyrene with poly(n-butyl acrylate) containing a small amount of tertiary amino groups

e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Kenji Yamamoto ◽  
Ayumi Nanakno ◽  
Hiroyasu Masunaga ◽  
Isamu Akiba
Keyword(s):  
Butyl Acrylate ◽  
Stoichiometric Composition ◽  
Phase Region ◽  
Molar Ratio ◽  
Amino Group ◽  
Amino Groups ◽  
Two Phase ◽  
Dimethylaminoethyl Methacrylate ◽  
X Ray Scattering ◽  
Tertiary Amino

Abstract Phase behavior in the blend of -SO3H terminated polystyrene (PSS) with poly(n-butyl acrylate-co-N,N-dimethylaminoethyl methacrylate) containing 6.0 mol% N,N-dimethylaminoethyl methacrylate (P1) is investigated by optical microscopy and small-angle X-ray scattering (SAXS). Comparing the miscibility of polystyrene/P1 blend, it is confirmed that the miscibility of the PSS/P1 blend is drastically improved by the hydrogen bonds between -SO3H and tertiary amino group. In addition, two-phase region of the PSS/P1 blend is split into two regions around the stoichiometric composition, in which the molar ratio of -SO3H to tertiary amino group is 1:1 stoichiometry. SAXS result shows that the PSS/P1 blend at stoichiometric composition forms a block copolymer-like aggregate and it takes a disorder state.

pKa-Werte von Ethidiumbromid und 7-Amino-9-phenyl-10- äthyl-phenanthridinium-bromid / pKa-Values of Ethidiumbromide and 7-Amino-9-phenyl-10-ethyl-phenanthridinium- bromide

1976 ◽  
Vol 31 (11-12) ◽  
pp. 656-660 ◽  
Author(s):  
Ingfried Zimmermann ◽  
Herbert Zimmermann
Keyword(s):  
Electronic Spectra ◽  
Water Solution ◽  
Ph Dependence ◽  
Quantum Mechanical ◽  
Amino Group ◽  
Quantum Mechanical Calculations ◽  
Acidic Water ◽  
Amino Groups ◽  
Electronic Density ◽  
Decreasing Ph

Abstract Ethidiumbromide (1) has two amino groups in 2-and 7-position which are protonated in acidic water solution. Both pKa-values of 1 are determined at 20 °C by means of the pH-dependence of the electronic spectra using a iterative calculating procedure, pKa1 = 0.713, pKa2 = 2.43. Acetylation of 1 and quantum mechanical calculations lead to the conclusion that the electronic density at the 7-amino group is greater than in 2-position. Therefore with decreasing pH preferably the 7-amino group is protonated (pKa2). followed by the protonation of the 2-amino group (pKa1). The pKa of 7-amino-9-phenyl-10-ethyl-phenanthridinium-bromide in water solution at 20 °C is determined to pKa= 1 .2 5 .

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