Kinetic Studies on the Acid Hydrolysis of Dextran

1978 ◽  
Vol 11 (4) ◽  
pp. 774-781 ◽  
Author(s):  
Arno Max Basedow ◽  
Klaus Heinrich Ebert ◽  
Hanns Josef Ederer
Keyword(s):  
Acid Hydrolysis ◽  
Kinetic Studies ◽  
Hydrolysis Of

scholarly journals Kinetic studies on the acid hydrolysis of the methyl ketoside of unsubstituted and O-acetylated N-acetylneuraminic acid

1973 ◽  
Vol 133 (4) ◽  
pp. 623-628 ◽  
Author(s):  
A. Neuberger ◽  
Wendy A. Ratcliffe
Keyword(s):  
Sialic Acid ◽  
Acid Hydrolysis ◽  
Model Compound ◽  
Kinetic Studies ◽  
Order Rate Constant ◽  
Neuraminic Acid ◽  
Acetylneuraminic Acid ◽  
Rate Of Hydrolysis ◽  
Ph Range ◽  
Hydrolysis Of

The hydrolysis of the model compound 2-O-methyl-4,7,8,9-tetra-O-acetyl-N-acetyl-α-d-neuraminic acid and neuraminidase (Vibrio cholerae) closely resembled that of the O-acetylated sialic acid residues of rabbit Tamm–Horsfall glycoprotein. This confirmed that O-acetylation was responsible for the unusually slow rate of acid hydrolysis of O-acetylated sialic acid residues observed in rabbit Tamm–Horsfall glycoprotein and their resistance to hydrolysis by neuraminidase. The first-order rate constant of hydrolysis of 2-methyl-N-acetyl-α-d-neuraminic acid by 0.05m-H2SO4 was 56-fold greater than that of 2-O-methyl-4,7,8,9-tetra-O-acetyl-N-acetyl -α-d-neuraminic acid. Kinetic studies have shown that in the pH range 1.00–3.30, the observed rate of hydrolysis of 2-methyl-N-acetyl-α-d-neuraminic acid can be attributed to acid-catalysed hydrolysis of the negatively charged CO2− form of the methyl ketoside.

Kinetic studies of two-stage sulphuric acid hydrolysis of sugarcane bagasse

2015 ◽  
Vol 83 ◽  
pp. 850-858 ◽  
Author(s):  
Sachin Kumar ◽  
Pratibha Dheeran ◽  
Surendra P. Singh ◽  
Indra M. Mishra ◽  
Dilip K. Adhikari
Keyword(s):  
Acid Hydrolysis ◽  
Sulphuric Acid ◽  
Sugarcane Bagasse ◽  
Kinetic Studies ◽  
Two Stage ◽  
Hydrolysis Of

scholarly journals Oxidation–reduction reactions of simple hydroxamic acids and plutonium(IV) ions in nitric acid

2008 ◽  
Vol 96 (6) ◽  
Author(s):  
M. J. Carrott ◽  
O. D. Fox ◽  
G. LeGurun ◽  
C. J. Jones ◽  
C. Mason ◽  
...  
Keyword(s):  
Acid Hydrolysis ◽  
Kinetic Studies ◽  
Hydroxamic Acids ◽  
Single Cycle ◽  
Fuel Cycles ◽  
Oxidation Reduction ◽  
Advanced Fuel ◽  
Extraction Processes ◽  
The Stability ◽  
Hydrolysis Of

SummarySimple hydroxamic acids such as formo- and aceto-hydroxamic acids have been proposed as suitable reagents for the separation of either Pu and/or Np from U in modified or single cycle Purex based solvent extraction processes designed to meet the emerging requirements of advanced fuel cycles. The stability of these hydroxamic acids is dominated by their decomposition through acid hydrolysis. Kinetic studies of the acid hydrolysis of formo- and aceto-hydroxamic acids are reported in the absence and the presence of Pu(IV) ions. The slow reduction of these plutonium(IV) hydroxamate complexes to Pu(III) aquo-ions has been characterised by spectrophotometry and cyclic voltammetry. The reductions of Pu(IV) in the presence of FHA and AHA are consistent with a mechanism in which free hydroxamic acid in solution is hydrolysed whilst Pu(IV) ions remain fully complexed to hydroxamate ligands; then at some point close to a 1 : 1 Pu(IV) : XHA ratio, some free Pu

Thiohydantoins. X. Kinetic Studies of the Acid Hydrolysis of 1-Acyl-2-thiohydantoins

1972 ◽  
Vol 50 (23) ◽  
pp. 3767-3779 ◽  
Author(s):  
Wayne Irvine Congdon ◽  
John Thomas Edward
Keyword(s):  
Sulfuric Acid ◽  
Carboxylic Acid ◽  
Acid Hydrolysis ◽  
Kinetic Studies ◽  
Steric Effects ◽  
Aqueous Sulfuric Acid ◽  
Hydrolysis Of

The rates of hydrolysis of 22 1-acyl-2-thiohydantoins in aqueous sulfuric acid to give 2-thiohydantoin and a carboxylic acid have been determined. In 0–90% sulfuric acid, hydrolysis takes place by an A-2 mechanism, and the rate reaches a maximum in about 70% acid. In acid more concentrated than about 90%, hydrolysis takes place by an A-1 mechanism, and the rate increases monotonically. Evidence for the two mechanisms comes from Yates r and Bunnett-Olsen [Formula: see text] parameters; from entropies of activation; from pσ and pσ+ relations; and from steric effects.

The Acid Hydrolysis of Egg Albumin. I. Kinetic Studies

1948 ◽  
Vol 70 (6) ◽  
pp. 2128-2131 ◽  
Author(s):  
Henry B. Bull ◽  
J. Wilfrid Hahn
Keyword(s):  
Acid Hydrolysis ◽  
Kinetic Studies ◽  
Egg Albumin ◽  
Hydrolysis Of

scholarly journals Kinetic Studies of Acid Hydrolysis of Food Waste-Derived Saccharides

2018 ◽  
Vol 57 (51) ◽  
pp. 17365-17374 ◽  
Author(s):  
Elvis Ebikade ◽  
Jonathan Lym ◽  
Gerhard Wittreich ◽  
Basudeb Saha ◽  
Dionisios G. Vlachos
Keyword(s):  
Acid Hydrolysis ◽  
Food Waste ◽  
Kinetic Studies ◽  
Hydrolysis Of

DETERMINATION OF MICRO-AMOUNTS OF 5β-PREGNAN-3α-OL-20-ONE IN URINE USING INFRARED-SPECTROMETRY

1962 ◽  
Vol 41 (2) ◽  
pp. 234-246 ◽  
Author(s):  
H. J. van der Molen
Keyword(s):  
Infrared Spectrum ◽  
Quantitative Determination ◽  
Acid Hydrolysis ◽  
Chromatographic Separation ◽  
Pure Form ◽  
Infrared Spectrometry ◽  
Hydrolysis Of

ABSTRACT A procedure for the quantitative determination of 5β-pregnan-3α-ol-20-one in urine is described. After acid hydrolysis of the pregnanolone-conjugates in urine, the free steroids are extracted with toluene. Pregnanolone is isolated in a pure form as its acetate; after chromatographic separation of the free steroids on alumina, the fraction containing pregnanolone is acetylated and rechromatographed on alumina. Quantitative determination of the isolated pregnanolone-acetate is carried out with the aid of the infrared spectrum recorded by a micro KBr-wafermethod. The reliability of the method under various conditions is discussed under the headings, specificity, accuracy, precision and sensitivity. It is possible to determine 30–40 μg pregnanolone in a 24-hours urine portion with a precision of 25%.

Sign in / Sign up

Export Citation Format

Share Document