Conversion of formaldehyde to acetic acid. Formic acid as a stoichiometric carbon monoxide-substitute

1985 ◽  
Vol 50 (25) ◽  
pp. 5376-5377 ◽  
Author(s):  
Leonard Kaplan
Keyword(s):  
Carbon Monoxide ◽  
Acetic Acid ◽  
Formic Acid

THE MECHANISM OF THE PHOTOOXIDATION OF ACETALDEHYDE AT ROOM TEMPERATURE

1959 ◽  
Vol 37 (10) ◽  
pp. 1671-1679 ◽  
Author(s):  
Jack G. Calvert ◽  
Philip L. Hanst
Keyword(s):  
Carbon Dioxide ◽  
Carbon Monoxide ◽  
Acetic Acid ◽  
Detection Limit ◽  
Formic Acid ◽  
Analytical Methods ◽  
Room Temperature ◽  
Product Formation ◽  
Infrared Spectrometry ◽  
Peroxyacetic Acid

The initial rates of product formation in the photooxidation of acetaldehyde at room temperature have been determined through the use of infrared spectrometry. The rates of formation of the products peroxyacetic acid, carbon monoxide, carbon dioxide, methanol, formic acid, and acetic acid were determined in experiments with various pressures of acetaldehyde, oxygen, and added gases. The amounts of methylhydroperoxide and acetylperoxide formed in all of the experiments were below the detection limit of the analytical methods. The results require that some modification and corrections be made to the mechanism suggested by McDowell and Sharples.

Confirmatory Tests for Aflatoxin B1

1964 ◽  
Vol 47 (5) ◽  
pp. 801-803 ◽  
Author(s):  
Peter John Andrellos ◽  
George R Reid
Keyword(s):  
Acetic Acid ◽  
Thin Layer ◽  
Formic Acid ◽  
Thionyl Chloride ◽  
Aflatoxin B1 ◽  
Trifluoroacetic Acid ◽  
Reaction Products ◽  
Confirmatory Tests ◽  
Aflatoxin B ◽  
Layer Chromatography

Abstract Three confirmatory tests have been devised to identify aflatoxin B±. Portions of the isolated toxin are treated with formic acid-thionyl chloride, acetic acid-thionyl chloride, and trifluoroacetic acid, respectively, and aliquots of the three fluorescent reaction products are spotted on thin-layer chromatography plates. Standards treated with each of the three reagents, plus an untreated standard, are spotted on the same plate, and after development the spots are compared under ultraviolet light.

Oxidation of carbon monoxide and formic acid on bulk and nanosized Pt–Co alloys

2011 ◽  
Vol 16 (2) ◽  
pp. 587-595 ◽  
Author(s):  
Maja D. Obradović ◽  
Amalija V. Tripković ◽  
Snežana Lj. Gojković
Keyword(s):  
Carbon Monoxide ◽  
Formic Acid ◽  
Co Alloys ◽  
Oxidation Of Carbon Monoxide

α-DEUTERIUM KINETIC ISOTOPE EFFECTS IN SOLVOLYSES OF endo-NORBORNYL p-BROMOBENZENESULFONATE

1965 ◽  
Vol 43 (8) ◽  
pp. 2254-2258 ◽  
Author(s):  
C. C. Lee ◽  
Edward W. C. Wong
Keyword(s):  
Acetic Acid ◽  
Formic Acid ◽  
Isotope Effects ◽  
Kinetic Isotope Effects ◽  
Aqueous Dioxane ◽  
Kinetic Isotope ◽  
Different Temperatures

endo-Norbornyl-2-d p-bromobenzenesulfonate was synthesized and the isotope effects, as measured by kH/kD, were determined over a range of temperatures for solvolyses in 30% water – 70% dioxane, acetic acid, and formic acid. Values of kH/kD are of the order of 1.20. The data appear to indicate slightly higher isotope effects as the solvents are changed from aqueous dioxane to acetic acid to formic acid, as well as somewhat higher isotope effects at lower temperatures. Possible mechanistic implications of these results are presented. Relative titrimetric acetolysis rates, kexo/kendo, at different temperatures, and enthalpies and entropies of activation for these acetolyses are evaluated and discussed.

scholarly journals Valorization of secondary feedstocks from the agroindustry by selective catalytic oxidation to formic and acetic acid using the OxFA process

2021 ◽  
Author(s):  
Sebastian Ponce ◽  
Stefanie Wesinger ◽  
Daniela Ona ◽  
Daniela Almeida Streitwieser ◽  
Jakob Albert
Keyword(s):  
Acetic Acid ◽  
Formic Acid ◽  
Reaction System ◽  
Value Added ◽  
Industrial Wastes ◽  
Raw Material ◽  
Gaseous Oxygen ◽  
Water As Solvent ◽  
Selective Catalytic Oxidation ◽  
Major Interest

AbstractThe selective oxidative conversion of seven representative fully characterized biomasses recovered as secondary feedstocks from the agroindustry is reported. The reaction system, known as the “OxFA process,” involves a homogeneous polyoxometalate catalyst (H8PV5Mo7O40), gaseous oxygen, p-toluene sulfonic acid, and water as solvent. It took place at 20 bar and 90 °C and transformed agro-industrial wastes, such as coffee husks, cocoa husks, palm rachis, fiber and nuts, sugarcane bagasse, and rice husks into biogenic formic acid, acetic acid, and CO2 as sole products. Even though all samples were transformed; remarkably, the reaction obtains up to 64, and 55% combined yield of formic and acetic acid for coffee and cocoa husks as raw material within 24 h, respectively. In addition to the role of the catalysts and additive for promoting the reaction, the influence of biomass components (hemicellulose, cellulose and lignin) into biogenic formic acid formation has been also demonstrated. Thus, these results are of major interest for the application of novel oxidation techniques under real recovered biomass for producing value-added products. Graphical abstract

Investigation on Formation and Solubility of Formic Acid, Acetic Acid and Levulinic Acid in Insulating Oil Using COSMO-RS

2021 ◽  
pp. 118256
Author(s):  
Enchen Yang ◽  
Hanbo Zheng ◽  
Tao Yang ◽  
Wei Yao ◽  
Zijian Wang ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Formic Acid ◽  
Levulinic Acid ◽  
Insulating Oil

scholarly journals Tropospheric Emission Spectrometer (TES) satellite observations of ammonia, methanol, formic acid, and carbon monoxide over the Canadian oil sands: validation and model evaluation

2015 ◽  
Vol 8 (12) ◽  
pp. 5189-5211 ◽  
Author(s):  
M. W. Shephard ◽  
C. A. McLinden ◽  
K. E. Cady-Pereira ◽  
M. Luo ◽  
S. G. Moussa ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Air Quality ◽  
Formic Acid ◽  
Model Evaluation ◽  
Oil Sands ◽  
Field Campaign ◽  
Infrared Observations ◽  
Multi Scale ◽  
Global Environmental ◽  
Scale Modelling

Abstract. The wealth of air quality information provided by satellite infrared observations of ammonia (NH3), carbon monoxide (CO), formic acid (HCOOH), and methanol (CH3OH) is currently being explored and used for a number of applications, especially at regional or global scales. These applications include air quality monitoring, trend analysis, emissions, and model evaluation. This study provides one of the first direct validations of Tropospheric Emission Spectrometer (TES) satellite-retrieved profiles of NH3, CH3OH, and HCOOH through comparisons with coincident aircraft profiles. The comparisons are performed over the Canadian oil sands region during the intensive field campaign (August–September, 2013) in support of the Joint Canada–Alberta Implementation Plan for Oil Sands Monitoring (JOSM). The satellite/aircraft comparisons over this region during this period produced errors of (i) +0.08 ± 0.25 ppbv for NH3, (ii) +7.5 ± 23 ppbv for CO, (iii) +0.19 ± 0.46 ppbv for HCOOH, and (iv) −1.1 ± 0.39 ppbv for CH3OH. These values mostly agree with previously estimated retrieval errors; however, the relatively large negative bias in CH3OH and the significantly greater positive bias for larger HCOOH and CO values observed during this study warrant further investigation. Satellite and aircraft ammonia observations during the field campaign are also used in an initial effort to perform preliminary evaluations of Environment Canada's Global Environmental Multi-scale – Modelling Air quality and CHemistry (GEM-MACH) air quality modelling system at high resolution (2.5 × 2.5 km2). These initial results indicate a model underprediction of ~ 0.6 ppbv (~ 60 %) for NH3, during the field campaign period. The TES/model CO comparison differences are ~ +20 ppbv (~ +20 %), but given that under these conditions the TES/aircraft comparisons also show a small positive TES CO bias indicates that the overall model underprediction of CO is closer to ~ 10 % at 681 hPa (~ 3 km) during this period.

Sign in / Sign up

Export Citation Format

Share Document