Curing alkyds

In some crosslinked polymer systems, like air-cured alkyd polyester paints, two separate Tlfi decay processes are observed. Longer Tlcs in these systems is associated with a more rigid environment for the spins the fractions of the two T1 populations indicate the amount of rigid and mobile protons, respectively 82). 

Petrex. [Hercules] Thermal-curing alkyd resin for inks. 

Foundry core binders are isocyanate-cured alkyd or phenolic adhesives used as binders for sand used to produce foundry sand molds. These sand molds are used to east iron and steel parts. A fast, economical cure of the sand mold is required under ambient conditions. 

Function 2 relates to the ability of the titanate molecule to transesterify. It implies the formation of chemical bonds between the titanate and the polymer matrix containing, for example, groups such as COOH and OH. Titanates can gel polyesters and epoxies and cure alkyds, even though there is no unsaturation in the titanate molecule backbone. 

For many moderate-duty films for operating temperatures below 80 to 120°C, M0S2 is used in combination with acryflcs, alkyds, vinyls, and acetate room temperature curing resins. For improved wear life and temperatures up to 150—300°C, baked coatings are commonly used with thermosetting resins, eg, phenohcs, epoxies, alkyds, siUcones, polyimides, and urethanes. Of these, the MlL-L-8937 phenoHc type is being appHed most extensively. 

Amino resins are also often used for the cure of other resins such as alkyds and reactive acryUc polymers. These polymer systems may contain 5—50% of the amino resin and are commonly used in the flexible backings found on carpets and draperies, as well as in protective surface coatings, particularly the durable baked enamels of appHances, automobiles, etc. 

Cured amino resins are far too brittle to be used alone as surface coatings for metal or wood substrates, but in combination with other film formers (alkyds, polyesters, acryUcs, epoxies) a wide range of acceptable performance properties can be achieved. These combination binder coating formulations cure rapidly at slightly elevated temperatures, making them well suited for industrial baking appHcations. The amino resin content in the formulation is typically in the range of 10—50% of the total binder soHds. 

The other broad class of refinish coatings is cross-linking coatings, caHed enamels in the trade. In the United States, most shops cure the enamels at room temperature in Europe, cure is commonly carried out at temperatures of 60—75°C. TraditionaHy, the vehicle was an oxidi2ing medium oH alkyd. 

The polyester alkyd moulding compositions are also based on a resin similar to those used for laminating. They are prepared by blending the resin with cellulose pulp, mineral filler, lubricants, pigments and peroxide curing agents on... 

The polyester alkyd resins are lower in cost than the DAP resins but are weaker mechanically, have a lower resistance to cracking round inserts and do not maintain their electrical properties so well under severe humid conditions. Fast-curing grades are available which will cure in as little as 20 seconds. 

Nitrile rubber is compatible with phenol-formaldehyde resins, resorcinol-formaldehyde resins, vinyl chloride resins, alkyd resins, coumarone-indene resins, chlorinated rubber, epoxies and other resins, forming compositions which can be cured providing excellent adhesives of high strength, high oil resistance and high resilience. On the other hand, NBR adhesives are compatible with polar adherends such as fibres, textiles, paper and wood. Specific formulations of NBR adhesives can be found in [12]. 

Urethane alkyds These are formed by the reaction of an isocyanate with alkyd, although the curing remains substantially through the oil-oxidation reaction. They have properties similar to alkyds although superior resistance to abrasion is claimed. 

Epoxy ester Epoxy esters are a type of alkyd where a high molecular weight resin is reacted with alkyd resin. The curing mechanism remains primarily through the oil-oxidation reaction and their properties are in no way similar to the chemically reacted epoxies. They have similar properties to alkyds although with improved chemical resistance but inferior appearance. They form a reasonably hard, oil-resistant coating, which can sometimes be suitable for machinery enamels, but are primarily for interior use, since they tend to chalk rapidly on exteriors. Their best use is for chemical or water resistance where circumstances dictate that finishes that are more superior cannot be used. 

Coating materials may be based on short or medium-oil alkyds (e.g. primers for door and window frames) nitrocellulose or thermoplastic acrylics (e.g. lacquers for paper or furniture finishes) amino resin-alkyd coatings, with or without nitrocellulose inclusions, but with a strong acid catalyst to promote low temperature cure (furniture finishes) two-pack polyurethanes (furniture, flat boards) unsaturated polyester resins in styrene with free-radical cure initiated by peroxides (furniture) or unsaturated acrylic oligomers and monomers cured by u.v. radiation or electron beams (coatings for record sleeves paperback covers, knock-down furniture or flush interior doors). 

Although rolling and dipping are sometimes used, power spray painting is the usual method of paint application. Among the coatings used are polyurethane, epoxy, acrylic, alkyd and vinyl based paints. With paints that are oven cured, products must have sufficient heat resistance to survive without distortion, etc. 

Uses. There are about forty to fifty organic peroxides commercially available in more than seventy formulations designed for specific applications which include (1) initiators for vinyl monomer polymerizations, and copolymerizations of monomers such as vinyl chloride, ethylene, styrene, vinyl acetate, acrylics, fluoroolefms and buta-dienestyrene (2) curing agents for thermoset polyesters, styrenated alkyds and oils, silicone rubbers and poly allyl diglycol carbonates ... 

Cure of alkyd resin A varnish is prepared by mixing 100 g of the alkyd resin prepared above, 0.05 g of Co(II) 2-ethylhexanoate, 0.05 g of calcium 2-etliyl-hexanoate, and 0.02 g of lead 2-ethylhexanoate. This mixture is held for 24 h in a closed flask before use. A thin layer of this varnish, applied on a metal plate, forms a hard, glossy coating after 24 h drying at room temperature. 

Urethane alkyds and urethane oils are oil and alkyd resin-modified polyurethanes dissolved in a volatile solvent. Upon application and solvent evaporation, the coating is crosslinked and cured via oxidation by atmospheric oxygen. 

Alkali metal (haloarylsulfonyl)thio-phenoxides, 364 Alkaline hydrolysis of nylon-6,6, 568-569 of PET, 549-550 Alkyd resins, 18, 30-31, 59-60 synthesis and cure of, 102 Alkylphenolic resins, 376 Alkylphenols, 376, 400 Allophanates, 227... 

The initial drying of currently applied alkyd paints is accomplished by evaporation of solvent (physical drying). Subsequently, the eventual curing of the alkyd paint is completed by the formation of a polymer network, which is mainly formed by chemical crosslinks (oxidative drying) but in some cases also physical interactions between the fatty acid side chains occur, such as crystallization or proton-bridge formation [129]. Efficient network formation is crucial in the formation of dry films with good mechanical properties. Due to the presence of unsaturated units in the investigated LOFA- and TOFA-PHA bin-... 

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