Determination of Coal in Formalin-Fixed Pneumoconiotic Lungs. A New Method of Tissue Digestion Using Glacial Acetic Acid.

1966 ◽  
Vol 38 (3) ◽  
pp. 441-444 ◽  
Author(s):  
Imanuel. Bergman
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
New Method ◽  
Formalin Fixed ◽  
Tissue Digestion

Determination of Piperazine in Formulations by Nonaqueous Titration

1963 ◽  
Vol 46 (6) ◽  
pp. 1060-1062
Author(s):  
R B Maybury ◽  
R Payfer
Keyword(s):  
Aqueous Solution ◽  
Acetic Acid ◽  
Perchloric Acid ◽  
Glacial Acetic Acid ◽  
Chloroform Solution ◽  
New Method ◽  
Alternative Procedure ◽  
Good Agreement

Abstract A new method is presented for the nonaqueous titration of piperazine in formulations in which the piperazine base is first brought into aqueous solution, and the solution is made strongly alkaline and extracted with chloroform. The chloroform solution of piperazine is then titrated with acetous perchloric acid to alpha-naphthol benzein indicator. The procedure is rapid, shows good agreement with other methods, and is applicable to most kinds of piperazine formulations. An alternative procedure for piperazine adipate, citrate, or tartrate in powders is given, in which the compound is dissolved and titrated directly in glacial acetic acid.

Reverse Phase Liquid Chromatographic Determination of Chlorophacinone and Diphacinone in Bait Formulations

1982 ◽  
Vol 65 (4) ◽  
pp. 927-929
Author(s):  
Brian R Bennett ◽  
Gregory S Grimes
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Chromatographic Determination ◽  
Reverse Phase ◽  
Target Concentration ◽  
External Standard ◽  
Liquid Chromatographic Determination ◽  
Phase Liquid ◽  
Liquid Chromatographic

Abstract Chlorophacinone and diphacinone are extracted at the 0.005% level from grain or paraffinized baits with glacial acetic acid. The target concentration is 0.01 mg/mL. The filtered supernate is chromatographed on a Partisil PXS ODS10/25 liquid chromatography column with premixed and degassed glacial acetic acid-tetrahydrofuran-water (14 + 2 + 9) and detected at 288 nm. The concentration is calculated by using an external standard. The recovery from spiked samples averaged 96.6% for both analytes. The response is linear from 0.001 to 0.040 mg/mL. The coefficient of variation of within-day replicates ranged from 1.1 to 2.5%.

A new method for the preparation of peroxymonophosphoric acid

2003 ◽  
Vol 81 (2) ◽  
pp. 156-160 ◽  
Author(s):  
Tian Zhu ◽  
Hou-min Chang ◽  
John F Kadla
Keyword(s):  
Hydrogen Peroxide ◽  
Acetic Acid ◽  
Carbon Tetrachloride ◽  
Glacial Acetic Acid ◽  
Acid Synthesis ◽  
Conversion Ratio ◽  
New Method ◽  
Phosphorous Pentoxide ◽  
Preparation Conditions ◽  
Peroxy Acids

A new method for the preparation of peroxymonophosphoric acid (H3PO5) has been developed. It utilizes a biphasic solution to moderate the vigorous reaction between phosphorous pentoxide (P2O5) and hydrogen peroxide (H2O2). P2O5 is suspended in carbon tetrachloride (CCl4), and concentrated H2O2 is slowly added while being vigorously stirred at low temperature. Careful control of the reaction temperature through the slow addition of H2O2 is critical. Using typical preparation conditions (P2O5:H2O2 = 0.5:1, H2O2 70 wt %, 2°C, 120–180 min), ~70% of the H2O2 is effectively converted to H3PO5. Increasing the concentration of H2O2, as well as the mole ratio of P2O5:H2O2, leads to an even higher % conversion of H2O2 to H3PO5. The addition of glacial acetic acid to the P2O5:H2O2 suspension at the end of the 120–180 min reaction (P2O5:H2O2:CH3COOH = 0.5:1:0.3) leads to the formation of peracetic acid in addition to H3PO5, and to an overall increase in the conversion ratio of total peroxy acids based on H2O2 (>95%).Key words: peroxymonophosphoric acid, synthesis, stability, conversion ratio.

Method for the accurate determination of specific rotation. Specific rotation of valine and leucine

1969 ◽  
Vol 47 (15) ◽  
pp. 2739-2746 ◽  
Author(s):  
J. C. MacDonald
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Optical Rotation ◽  
Accurate Determination ◽  
Computer Calculation ◽  
Specific Rotation ◽  
Best Fit

The optical rotation of various concentrations of L-valine and L-leucine, dissolved in glacial acetic acid, or 5 or 6 M HCl, was measured with a photoelectric polarimeter at the nominal wavelengths 589, 578, 546, 436, and 365 nm and temperatures of 20, 25, and 30 °C. The specific rotation for any one wavelength, solute, and solvent could be defined by the equation [α]λT = A(1 + D(T − 25)) + BC, where T is temperature in °C, C is concentration in grams of solute per 100 ml of solution, and A, B, and D are constants. The best fit values of the constants were determined by computer calculation and are listed. Constants are also given for calculating a specific rotation based on grams of solute per 100 g of solution.

Determination of acetaldehyde in glacial acetic acid by gas chromatography

1974 ◽  
Vol 46 (11) ◽  
pp. 1584-1584 ◽  
Author(s):  
Harold J. Rhodes ◽  
David W. Bode ◽  
Martin I. Blake
Keyword(s):  
Gas Chromatography ◽  
Acetic Acid ◽  
Glacial Acetic Acid

Bromination of Acridine

2018 ◽  
Vol 71 (4) ◽  
pp. 285
Author(s):  
Graham S. Chandler ◽  
Wolfgang H. F. Sasse
Keyword(s):  
Acetic Acid ◽  
Sulfuric Acid ◽  
Quantitative Determination ◽  
Glacial Acetic Acid ◽  
Tiny Amount ◽  
Concentrated Sulfuric Acid

The quantitative determination of the products of bromination of acridine in concentrated sulfuric acid and glacial acetic acid is described. In both cases, the only monobromo products were the 2- and 4-substituted compounds. With sulfuric acid, the 4-isomer predominates whereas in acetic acid, the 2-isomer is predominant. This work expands substantially on the tiny amount of previous work on halogenation of dibenzo-annelated pyridines.

Use of Glacial Acetic Acid in the Determination of Metol in Developer Solutions

1951 ◽  
Vol 57 (5) ◽  
pp. 411-415 ◽  
Author(s):  
William R. Crowell ◽  
Harvey E. Gausman ◽  
Harlan L. Baumbach
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid
Sign in / Sign up

Export Citation Format

Share Document