Resin preparation and

Unsaturated polyesters (UPs), 4, 18, 19 from PET waste, 560-561 Unsaturated polyester/styrene resin, preparation and cure of, 101 Unsaturated polyester thermosetting resins, syntheses of, 101-103 Unstirred interfacial process, 155 U-Polymer, 77... 

Ion exchange polar, nonpolar large volumes, organic recovery 70-90% resin preparation and elution 18, 24, 25... 

Junk et al. (5) found that the Rohm and Haas procedure (29) did not clean the resin sufficiently for use as an adsorbent for recovering nanogram-per-liter amounts of organic materials. Junk s resin preparation and cleaning procedure started with backwashing the resin with water to remove fines, sodium chloride, and sodium carbonate. 

The bond performances of lignin-phenolic resin systems were studied through a series of experiments, each designed to elucidate a facet of the problem. The resin preparation and panel fabrication procedures were, however, maintained as uniformly as possible. Thus, unless otherwise specified, the experimental procedures described below were used in the study. 

Madders. Phenolic polymers are known to have high rigidity, and this property extends to phenolic foams, which are highly friable. In order to reduce friabUity and permit some flexibUity and toughness, various kinds of modifiers are sometimes used. Reactive modifiers are used in the course of resol-resin preparation, and they become integral parts of the polymer structure. Examples include PVA (polyvinyl alcohol), PVA-PVC (polyvinyl alcohol-polyvinyl chloride-copolymer), resorcinol, o-cresol, furfuryl alcohol, and other various types of polyols. 

The chemical and physical characteristics of phenolic resins and adhesives made from them suggest that formaldehyde emissions should be very minor ( 1 ). One reason for predicting low emissions is that very little residual free formaldehyde is present in prepared phenolic resins. This low free formaldehyde content is due to both the use of low formaldehyde to phenol mole ratios in resin preparation and to the tendency of nearly all the formaldehyde to react irreversably with the phenol. 

Some of the typical reactions that take place during an alkyd resin preparation and curing are (1) esterification, (2) alcoholysis, (3) ester interchange or transesterification, (4) etherification, (5) free radical addition reactions, (6) Diels-Alder reactions, (7) decarboxylations, and (8) polymerization via free radical initiation during curing (air-drying alkyds). 

McK1972 McKinley, S.V. and Rakshys, J.W. Jr., Wittig Resins. Preparation and Application of Insoluble Polymeric Phospho-ranes, J. Chem. Soc., Chem. Commun., (1972) 134-135. 

Obtained by K.OH fusion of many resins. Prepared by fusion of m-benzenedisulphonic acid with caustic soda, also obtained to some extent in the NaOH fusion of o-and p-ben-zenedisulphonic acids. 

Furfural has been used as a component in many resin appHcations, most of them thermosetting. A comprehensive review of the patent Hterature describing these uses is beyond the scope of this review. A few, selected recent patents and journal articles have been referenced. Resins prepared from the condensation products of furfural with urea (47), formaldehyde (48), phenols (49,50), etc, modified by appropriate binders and fillers are described in the technical Hterature for earlier appHcations, see reference 1, which contains many references in an appendix. 

In addition, boron trifluoride and some of its adducts have widespread appflcation as curing agents for epoxy resins (qv), and in preparing alcohol-soluble phenoflc resins (qv) (41). 

Foaming polystyrene resin prepared by blending with gas deHvers an opaque, low density sheet useful for beverage-bottle and plastic can labels as a water-resistant paper substitute (see Styrene polymers). 

Epoxy Resins. Urethane and ester-extended hydantoia epoxy resins cured with several compounds seem to have better properties than the previous ones (98). These resins are prepared from hydantoias such as (21) (99,100). 

Unsaturated polyester resins prepared by condensation polymerization constitute the largest industrial use for maleic anhydride. Typically, maleic anhydride is esterified with ethylene glycol [107-21-1] and a vinyl monomer or styrene is added along with an initiator such as a peroxide to produce a three-dimensional macromolecule with rigidity, insolubiUty, and mechanical strength. 

Naphthalenediol. This diol is made by the fusion of sodium 2,7-naphthalenedisulfonate with molten sodium hydroxide at 280—300°C in ca 80% yield. A formaldehyde resin prepared from this diol has excellent erosion resistance, strength, and chemical inertness it is used as an ablative material in rocket-exhaust environments (76). 

Second, in the early 1950s, Hogan and Bank at Phillips Petroleum Company, discovered (3,4) that ethylene could be catalyticaHy polymerized into a sohd plastic under more moderate conditions at a pressure of 3—4 MPa (435—580 psi) and temperature of 70—100°C, with a catalyst containing chromium oxide supported on siUca (Phillips catalysts). PE resins prepared with these catalysts are linear, highly crystalline polymers of a much higher density of 0.960—0.970 g/cnr (as opposed to 0.920—0.930 g/cnf for LDPE). These resins, or HDPE, are currentiy produced on a large scale, (see Olefin polymers, HIGH DENSITY POLYETHYLENE). 

Resoles. The advancement and cure of resole resins foUow reaction steps similar to those used for resin preparation the pH is 9 or higher and reaction temperature should not exceed 180°C. Methylol groups condense with other methylols to give dibenzyl ethers and react at the ortho and para positions on the phenol to give diphenyknethylenes. In addition, dibenzyl ethers eliminate formaldehyde to give diphenyknethanes. 

Neoprene—phenohc contact adhesives, known for thein high green strength and peel values, contain a resole-type resin prepared from 4-/-butylphenol. The alkyl group increases compatibiHty and reduces cross-linking. This resin reacts or complexes with the metal oxide, eg, MgO, contained in the formulation, and increases the cohesive strength of the adhesive. In fact, the reactivity with MgO is frequently measured to determine the effectiveness of heat-reactive phenoHcs in the formulation. 

The neat resin preparation for PPS is quite compHcated, despite the fact that the overall polymerization reaction appears to be simple. Several commercial PPS polymerization processes that feature some steps in common have been described (1,2). At least three different mechanisms have been pubUshed in an attempt to describe the basic reaction of a sodium sulfide equivalent and -dichlorobenzene these are S Ar (13,16,19), radical cation (20,21), and Buimett s (22) Sj l radical anion (23—25) mechanisms. The benzyne mechanism was ruled out (16) based on the observation that the para-substitution pattern of the monomer, -dichlorobenzene, is retained in the repeating unit of the polymer. Demonstration that the step-growth polymerization of sodium sulfide and /)-dichlorohenzene proceeds via the S Ar mechanism is fairly recent (1991) (26). Eurther complexity in the polymerization is the incorporation of comonomers that alter the polymer stmcture, thereby modifying the properties of the polymer. Additionally, post-polymerization treatments can be utilized, which modify the properties of the polymer. Preparation of the neat resin is an area of significant latitude and extreme importance for the end user. 

A wide variety of organosiUcone resins containing a combination of M, D, T, and/or Q groups have been prepared and many are commercially manufactured. In addition, resins containing hydrosilation-reactive SiH and SiVi groups or other functionahties, including OH and phenyl groups, are known. Two classes of sihcone resins are most widely used in the sihcone industry MQ and TD resins. 

There was a tendency to use these resins mixed with urea—formaldehyde or melamine-type resins. Preparation of pure tria2ones or uron resins is difficult and expensive (61,62). Furthermore, the basic nature of the amine nitrogen in tria2one permits the use of mixtures of tria2ones with other agents to yield finishes that retain strength in hypochlorite bleaching. 

Vinylidene Chloride Copolymer Latex. Vinyhdene chloride polymers are often made in emulsion, but usuaUy are isolated, dried, and used as conventional resins. Stable latices have been prepared and can be used direcdy for coatings (171—176). The principal apphcations for these materials are as barrier coatings on paper products and, more recently, on plastic films. The heat-seal characteristics of VDC copolymer coatings are equaUy valuable in many apphcations. They are also used as binders for paints and nonwoven fabrics (177). The use of special VDC copolymer latices for barrier laminating adhesives is growing, and the use of vinyhdene chloride copolymers in flame-resistant carpet backing is weU known (178—181). VDC latices can also be used to coat poly(ethylene terephthalate) (PET) bottles to retain carbon dioxide (182). 

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