Results 181 to 190 of about 12,733 (226)
Some of the next articles are maybe not open access.
The chemistry of furfuryl alcohol resins
Journal of Applied Polymer Science, 1971AbstractFurfuryl alcohol resins contain a broad spectrum of compounds. The distribution of these compounds in a given resin varies with the manufacturing conditions. A resin containing a high proportion of low molecular weight constituents has been prepared and separated into fractions.
J. B. Barr, S. B. Wallon
openaire +1 more source
Chemically Activated Furfuryl Alcohol-Based Wood Adhesives. I. The Role of Furfuryl Alcohol
hfsg, 1996Composite boards were prepared using wood powder as a matrix and furfuryl alcohol (FA) or polyfurfuryl alcohol (PFA) as a binder with hydrogen peroxide/ferrous ion or nitric acid as an activator. PFA gave a board with tensile strength and water resistance superior to that obtained with FA ; the PFA degree of polymerization exerted a positive influence ...
Lan Thuy Dao, Eugene Zavarin
openaire +1 more source
Kinetics of homopolycondensation of furfuryl alcohol
Polymer Science Series B, 2007The kinetic features of the homopolycondensation of furfuryl alcohol in an aqueous medium in the presence of acids of different strengths have been studied. The second order of the reaction with respect to the monomer has been established. A kinetic scheme of the polycondensation reaction has been proposed, and the activation parameters of the process ...
M. G. Alimukhamedov, F. A. Magrupov
openaire +1 more source
The versatility of furfuryl alcohols and furanoxonium ions in synthesis
Chemical Communications, 2014Substituted furfuryl alcohols are extraordinarily versatile starting materials in synthesis. They are precursors to furanoxonium ion intermediates which are implicated in the Piancatelli reaction (leading to 2-cyclopentenones) and in the synthesis of novel dihydrofuran-based exo enol ether/cyclic ketal natural products. They are also intermediates in a
Matthew J, Palframan, Gerald, Pattenden
openaire +2 more sources
Journal of Applied Polymer Science, 2007
AbstractGlassy carbon can be manufactured practically without pores, named Monolithic Vitreous Carbon (MVC) or presenting up to 98% in transport pore volume, foam form, denominated Reticulated Vitreous Carbon (RVC). The glassy carbon processing is affected by some processing parameters, among them it can be cited the resin viscosity.
Gaefke, C. B. +3 more
openaire +2 more sources
AbstractGlassy carbon can be manufactured practically without pores, named Monolithic Vitreous Carbon (MVC) or presenting up to 98% in transport pore volume, foam form, denominated Reticulated Vitreous Carbon (RVC). The glassy carbon processing is affected by some processing parameters, among them it can be cited the resin viscosity.
Gaefke, C. B. +3 more
openaire +2 more sources
Thermochimica Acta, 2015
Abstract Densities (ρ) and sound velocities (u) of the pure liquids obtained from different biomass conversion: furfural, furfuryl alcohol, toluene, and ethanol were measured at temperature range from 283.15 K to 313.15 K at 10 K interval using a vibrating tube densimeter and sound velocity analyzer (Anton Paar DSA 5000M). Besides that, the densities
M. Zaoui-Djelloul-Daouadji +6 more
openaire +2 more sources
Abstract Densities (ρ) and sound velocities (u) of the pure liquids obtained from different biomass conversion: furfural, furfuryl alcohol, toluene, and ethanol were measured at temperature range from 283.15 K to 313.15 K at 10 K interval using a vibrating tube densimeter and sound velocity analyzer (Anton Paar DSA 5000M). Besides that, the densities
M. Zaoui-Djelloul-Daouadji +6 more
openaire +2 more sources
Synthesis of furfuryl alcohol and furoic acid
Journal of Chemical Education, 1978The exercise in this paper can be conducted utilizing two 3-hour laboratory periods and is meant to illustrate the 1) the use of the cannizzaro reaction in synthesis, 2) production of a commercial ...
openaire +1 more source
5-(Diethylaminomethyl) Furfuryl Alcohol
1959A solution of 10.5 g (0.05 mole) of methyl 5-(diethylaminomethyl)-2-furoate (see p. 22), b.p. 102–103° /1.5 mm, in 150 ml of dry ether was added dropwise over a period of 0.5–1 hour to a stirred ethereal solution (200 ml) of lithium aluminum hydride (Note 1) contained in a 500-ml three-necked flask fitted with mercury-sealed stirrer, dropping funnel ...
openaire +1 more source
The Nature of Furfuryl Alcohol
Industrial & Engineering Chemistry, 1942A. P. Dunlop, Fredus N. Peters
openaire +1 more source

