Alkaline hydrolysis of bridged and monodentate sulfato complexes of cobalt(III). X-ray structure of [Co(en)2(OS(O2)O)]2ZnCl4.cntdot.H2O containing cis-bis(.mu.-sulfato) bridges

1988 ◽  
Vol 27 (20) ◽  
pp. 3544-3547 ◽  
Author(s):  
David A. Buckingham ◽  
Charles R. Clark ◽  
Jim Simpson ◽  
Ward T. Robinson
Keyword(s):  
Alkaline Hydrolysis ◽  
X Ray ◽  
Hydrolysis Of ◽  
Sulfato Complexes

scholarly journals Stereoselective synthesis and transformation of pinane-based 2-amino-1,3-diols

2021 ◽  
Vol 17 ◽  
pp. 983-990
Author(s):  
Ákos Bajtel ◽  
Mounir Raji ◽  
Matti Haukka ◽  
Ferenc Fülöp ◽  
Zsolt Szakonyi
Keyword(s):  
Alkaline Hydrolysis ◽  
Stereoselective Synthesis ◽  
2D Nmr ◽  
Ring Closure ◽  
Spectroscopic Techniques ◽  
Reductive Alkylation ◽  
X Ray ◽  
Relative Stereochemistry ◽  
Hydrolysis Of

A library of pinane-based 2-amino-1,3-diols was synthesised in a stereoselective manner. Isopinocarveol prepared from (−)-α-pinene was converted into condensed oxazolidin-2-one in two steps by carbamate formation followed by a stereoselective aminohydroxylation process. The relative stereochemistry of the pinane-fused oxazolidin-2-one was determined by 2D NMR and X-ray spectroscopic techniques. The regioisomeric spiro-oxazolidin-2-one was prepared in a similar way starting from the commercially available (1R)-(−)-myrtenol (10). The reduction or alkaline hydrolysis of the oxazolidines, followed by reductive alkylation resulted in primary and secondary 2-amino-1,3-diols, which underwent a regioselective ring closure with formaldehyde or benzaldehyde delivering pinane-condensed oxazolidines. During the preparation of 2-phenyliminooxazolidine, an interesting ring–ring tautomerism was observed in CDCl3.

scholarly journals Synthesis and transformation of sphingosine analogue pinane-based 2-amino-1,3-diols

2021 ◽  
Author(s):  
Ákos Bajtel ◽  
Mounir Raji ◽  
Matti Haukka ◽  
Ferenc Fülöp ◽  
Zsolt Szakonyi
Keyword(s):  
Alkaline Hydrolysis ◽  
2D Nmr ◽  
Ring Closure ◽  
Biologically Active ◽  
Reductive Alkylation ◽  
X Ray ◽  
Relative Stereochemistry ◽  
Hydrolysis Of

A library of pinane-based 2-amino-1,3-diols, analogues of biologically active sphingosine, was synthesised in a stereoselective manner. Isopinocarveol prepared from (–)-α-pinene was converted to condensed oxazolidin-2-one in two steps by carbamate formation followed by a stereoselective aminohydroxylation process. The relative stereochemistry of the pinane-fused oxazolidin-2-one was determined by 2D NMR and X-ray technics. The regioisomeric spiro-oxazolidin-2-one was prepared in a similar way starting from commercially available (1R)-(–)-myrtenol. Reduction or alkaline hydrolysis of oxazolidines followed by reductive alkylation resulted in primary and secondary 2-amino-1,3-diols, which underwent regioselective ring closure with formaldehyde or benzaldehyde delivering pinane-condensed oxazolidines. During the preparation of 2-phenyliminooxazolidine, an interesting ring–ring tautomerism was observed in CDCl3.

scholarly journals Characterization and Optimization of the Alkaline Hydrolysis of Polyacrylonitrile Membranes

Polymers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1843 ◽  
Author(s):  
Leyre Pérez-Álvarez ◽  
Leire Ruiz-Rubio ◽  
Isabel Moreno ◽  
José Luis Vilas-Vilela
Keyword(s):  
Mechanical Properties ◽  
Alkaline Hydrolysis ◽  
Photoelectron Spectroscopy ◽  
Reaction Times ◽  
Special Importance ◽  
X Ray ◽  
Carboxylic Acid Groups ◽  
Wide Range ◽  
Enhanced Properties ◽  
Hydrolysis Of

There is currently an increasing interest in the development of polyacrylonitrile (PAN)-based membranes with new and enhanced properties which are of special importance in the processes of pervaporation, purification, and water treatment. Thus, the optimization of the functionalization of PAN membranes and its effect on their morphology, hydrophilicity, and mechanical properties plays an essential role in a wide range of applications. In this paper, the alkaline hydrolysis of asymmetric PAN membranes was investigated in order to get carboxyl-enriched surfaces that are of a great interest for more demanding subsequent modifications. The process was monitored using –C=NH intermediate bonds, which could be observed during the hydrolysis reaction by X-Ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FTIR) before the formation of carboxyl and amide groups. The amount of introduced carboxylic acid groups could be determined by thermogravimetric analysis (TGA) and by the interaction with toluidine blue O (TBO) dye. Hydrolysis was revealed as a simple way to modulate hydrophilicity (decreasing contact angle from 60 to 0° for reaction times from 0–3 h) and the mechanical properties of PAN membranes.

A new insight on alkaline hydrolysis of calcium aluminate cement concrete: Part I. Fundamentals

1996 ◽  
Vol 11 (7) ◽  
pp. 1748-1754 ◽  
Author(s):  
S. Goñi ◽  
C. Andrade ◽  
J. L. Sagrera ◽  
M. S. Hernández ◽  
C. Alonso
Keyword(s):  
Calcium Aluminate ◽  
Alkaline Hydrolysis ◽  
Degradation Process ◽  
Calcium Aluminate Cement ◽  
X Ray Diffraction ◽  
Cement Concrete ◽  
X Ray ◽  
Concrete Part ◽  
Hydrolysis Of ◽  
Aluminate Cement

In this work a hypothesis to explain the alkaline hydrolysis degradation process of calcium aluminate cement concrete (CACC) is presented. The hypothesis is based on x-ray diffraction (XRD) data of some samples taken from real Spanish CACC structures. The identification from XRD data of a hydrated alkaline aluminate could serve as a guide to differentiate both processes of normal carbonation and alkaline hydrolysis.

Identification of acid-insoluble filter-plugging compounds and optimal acid-washing procedures for tubular backpulse pressure filters

TAPPI Journal ◽  
2011 ◽  
Vol 10 (1) ◽  
pp. 17-23
Author(s):  
KEVIN TAYLOR ◽  
RICH ADDERLY ◽  
GAVIN BAXTER
Keyword(s):  
Calcium Sulfate ◽  
Membrane Filter ◽  
Sulfamic Acid ◽  
Xrd Analysis ◽  
Metal Sulfides ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gypsum Formation ◽  
Acid Washing ◽  
Hydrolysis Of

Over time, performance of tubular backpulse pressure filters in kraft mills deteriorates, even with regular acid washing. Unscheduled filter replacement due to filter plugging results in significant costs and may result in mill downtime. We identified acid-insoluble filter-plugging materials by scanning electron microscope/energy-dispersion X-ray spectroscopy (SEM/EDS) and X-ray diffraction (XRD) analysis in both polypropylene and Gore-Tex™ membrane filter socks. The major filter-plugging components were calcium sulfate (gypsum), calcium phosphate (hydroxylapatite), aluminosilicate clays, metal sulfides, and carbon. We carried out detailed sample analysis of both the standard acid-washing procedure and a modified procedure. Filter plugging by gypsum and metal sulfides appeared to occur because of the acid-washing procedure. Gypsum formation on the filter resulted from significant hydrolysis of sulfamic acid solution at temperatures greater than 130°F. Modification of the acid-washing procedure greatly reduced the amount of gypsum and addition of a surfactant to the acid reduced wash time and mobilized some of the carbon from the filter. With surfactant, acid washing was 95% complete after 40 min.

Influence of medium on alkaline hydrolysis of succinic acid monomethyl and monopropyl esters

1980 ◽  
Vol 45 (11) ◽  
pp. 2873-2882
Author(s):  
Vladislav Holba ◽  
Ján Benko
Keyword(s):  
Succinic Acid ◽  
Kinetic Parameters ◽  
Alkaline Hydrolysis ◽  
Specific Interactions ◽  
Nonaqueous Media ◽  
The Media ◽  
Kinetics Of ◽  
Hydrolysis Of

The kinetics of alkaline hydrolysis of succinic acid monomethyl and monopropyl esters were studied in mixed aqueous-nonaqueous media at various temperatures and ionic strengths. The results of measurements are discussed in terms of electrostatic and specific interactions between the reactants and other components of the reaction mixture. The kinetic parameters in the media under study are related to the influence of the cosolvent on the solvation sphere of the reactants.

Investigation of the products of carbothermal reduction of yttrium oxide by the hydrolysis method

1984 ◽  
Vol 49 (4) ◽  
pp. 936-943 ◽  
Author(s):  
Bohumil Hájek ◽  
Pavel Karen ◽  
Vlastimil Brožek
Keyword(s):  
Yttrium Oxide ◽  
Carbothermal Reduction ◽  
Stoichiometric Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrolysis Method ◽  
Sample Decomposition ◽  
Products Of Reaction ◽  
Hydrolysis Of ◽  
Lower Carbon

For the investigation of the products of reaction of yttrium oxide with carbon mixed in various proportions, the chemical and X-ray diffraction methods of analysis were combined with the gas chromatographic analysis of the mixture of hydrocarbons and hydrogen formed on the sample decomposition with water. The carboreduction of Y2O3 was examined at relatively low temperatures, convenient for obtaining the reaction intermediates in higher yields. At 1 600 °C and pressures of 10-3 Pa the reduction of a mixture of Y2O3 with carbon in a stoichiometric ratio of 1 : 7 yields YC2 in equilibrium with 20% of Y2OC phase. At lower carbon contents (down to the Y2O3 : C ratio of 1 : 2) tha fraction of the Y2OC phase increases up to approximately 30%. In addition to Y2O3, the reaction mixture contains also Y2C, Y2OC and a phase giving propyne on hydrolysis. The presence of traces of C3 hydrocarbons and small amounts of methane in the product of hydrolysis of the carbide sample prepared by the carbothermal reduction of the oxide can be explained in terms of the occurrence of the Y15C19 phase, probably substituted in part by oxygen, and of the Y2OC phase. The results are compared with those obtained previously for the Sc2O3 + C system.

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