Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Acetic acid bond strengths

The PVF is made by acidic reaction between poly(vinyl alcohol) (PVA) and formaldehyde. The poly(vinyl alcohol) is, in turn, made by hydrolysis of poly(vinyl acetate) or transesterification of poly(vinyl acetate). Thus, residual alcohol and ester functionality is usually present. Cure reportedly occurs through reaction of phenolic polymer hydroxyls with the residual hydroxyls of the PVA [199]. The ester residues are observed to reduce bond strength in PVF-based systems [199]. This does not necessarily extend to PVF-P adhesives. PVF is stable in strong alkali, so participation of the acetals in curing is probably unimportant in most situations involving resoles. PVF is physically compatible with many phenolic resins. [Pg.928]

The distance from each hydrogen atom to the nearer of the two adjacent oxygen atoms in the dimer of acetic acid has been reported to be 1.075 0.015 A this is considerably greater than the value 1.01 A for ice, as is to be expected in consequence of the increased strength of the hydrogen bond. [Pg.477]

C. Epoxy ROSins. The epoxy resins are thermosetting plastics which have great strength and the ability to form tenacious bonds with most surfaces. Furthermore, the cured resin is resistant to many solvents and chemicals. (Some epoxy resins are decomposed by acetic acid, and all are attacked by very strong oxidizing agents.) Because of this combination of properties, epoxy cements are frequently used to bond metal, glass, wood, and plastics. [Pg.140]

Epoxies, isocyanate cured polyester, and cyanoacrylates are used to bond acetal copolymer. Generally, the surface is treated with sulfuric-chromic acid. Epoxies have shown 150- to 500-psi shear strength on sanded surfaces and 500- to 1000-psi on chemically treated surfaces. Two-component epoxies give slightly lower bond strengths. However, they bond acetal to itself and to many other materials. [Pg.368]

Acetal (copolymer) Acetone 1. Abrasion. Grit or vapor blast, or medium-grit emery cloth followed by solvent degreasing. 2. Etch in the following acid solution for 10 s at 25°C Potassium dichromate 75 Distilled water 120 Sulfuric acid (96%) 1500 Rinse in distilled water, dry in air at RT. For general-purpose bonding For maximum bond strength. ASTM D 2093... [Pg.500]

For example, in acetic acid the bond strengths are surprising. The strongest bond is the 0-H bond and the weakest is the C-C bond. Yet very few reactions... [Pg.288]

Initially the mobile phase was too strong and elutes all of the compounds at V0 The mobile phase strength is decreased stepwise until all four components are resolved. It is important to reemphasize that when using ion suppression, the additive used to adjust the pH must remain at a constant concentration during the method development process. Also, it should be mentioned that while acetic acid adjusts the pH to an approximate value of 3 and is often used in ion suppression, it is not a buffer. Therefore, use of a sodium acetate buffer (0.001 to 0.01 M) may be more appropriate for some bonded phases. [Pg.157]


See other pages where Acetic acid bond strengths is mentioned: [Pg.89]    [Pg.468]    [Pg.121]    [Pg.307]    [Pg.533]    [Pg.534]    [Pg.99]    [Pg.101]    [Pg.9]    [Pg.58]    [Pg.73]    [Pg.199]    [Pg.704]    [Pg.204]    [Pg.575]    [Pg.104]    [Pg.109]    [Pg.109]    [Pg.104]    [Pg.115]    [Pg.76]    [Pg.55]    [Pg.157]    [Pg.337]    [Pg.780]    [Pg.800]    [Pg.93]    [Pg.611]    [Pg.612]    [Pg.183]    [Pg.173]    [Pg.187]    [Pg.126]    [Pg.468]    [Pg.116]    [Pg.273]    [Pg.284]    [Pg.286]    [Pg.294]    [Pg.332]    [Pg.343]    [Pg.126]    [Pg.127]   
See also in sourсe #XX -- [ Pg.207 ]




SEARCH



Acetal bonds

Acetic acid strength

Acid strength

Acidizing strength

Acids bond strength

Acids, acid strength

Bond strength

Bonding strength

© 2024 chempedia.info