N methyl methacrylate

In the case of good solvent power, x, is approximately given by the Rouse relaxation time which corroborates the basic assumptions of the Graessley theory. However, in a poor solvent and in the vicinity of demixing the ratio X(,/x increases which clearly demonstrates the reduced mobility of the polymer chains under these circumstances. A similar feature can be observed in the course of the study of the poly(n-methyl methacrylate)s Figure 11 shows the shift factor Xq divided by the corresponding quantity obtained at the same concentration in a good solvent. 

San Roman and co-workers [161] studied the microstructure and stereochemical configuration of methacrylonitrile (N), methyl methacrylate (M), copolymers prepared by free-radical polymerisation at 60 C on the basis of the classical terminal copolymerisation model and with the assumption of Bernoullian statistics for the... 

Acryhc stmctural adhesives have been modified by elastomers in order to obtain a phase-separated, toughened system. A significant contribution in this technology has been made in which acryhc adhesives were modified by the addition of chlorosulfonated polyethylene to obtain a phase-separated stmctural adhesive (11). Such adhesives also contain methyl methacrylate, glacial methacrylic acid, and cross-linkers such as ethylene glycol dimethacrylate [97-90-5]. The polymerization initiation system, which includes cumene hydroperoxide, N,1S7-dimethyl- -toluidine, and saccharin, can be apphed to the adherend surface as a primer, or it can be formulated as the second part of a two-part adhesive. Modification of cyanoacrylates using elastomers has also been attempted copolymers of acrylonitrile, butadiene, and styrene ethylene copolymers with methylacrylate or copolymers of methacrylates with butadiene and styrene have been used. However, because of the extreme reactivity of the monomer, modification of cyanoacrylate adhesives is very difficult and material purity is essential in order to be able to modify the cyanoacrylate without causing premature reaction. 

Fig. 12. Viscosity at different temperatures measured by a capillary viscometer injection-molding grade of poly(methyl methacrylate) (43). To convert N/m to psi, multiply by 145 to convert (N-s)/m to (dyn-s)/cm (P), multiply by 10.

The successful development of eye contact lenses led in turn to a demand for soft contact lenses. Such a demand was eventually met by the preparation of copolymers using a combination of an acrylic ester monomer such as methyl methacrylate, a cross-linkable monomer such as a dimethacrylate, and a monomer whose homopolymer is soluble or highly swollen in water such as N-vinyl pyrrolidone. Such copolymers swell in water (hence the term hydrophilic), the degree of swelling being controlled by the specific type and amount of the monomers used. In use the lens is swollen to equilibrium in water, a typical soft lens having a water content of about 75%. 

The reported values for the exponent of the monomer concentration for the rate of polymerization were found to be 1.26[61], 1.3[16] for gamma radiation-induced copolymerization of acrylamide with N,N-di-ethyldiallylammonium chloride and methyl chloride salt of /V,N-dimethylaminoethyl methacrylate (DMAEM-MC). Ishigue and Hamielec [34] have shown that the... 

In contrast to /3-PCPY, ICPY did not initiate copolymerization of MMA with styrene [39] and AN with styrene [40]. However, it accelerated radical polymerization by increasing the rate of initiation in the former case and decreasing the rate of termination in the latter case. The studies on photocopolymerization of MMA with styrene in the presence of ICPY has also been reported [41], /8-PCPY also initiated radical copolymerization of 4-vinylpyridine with methyl methacrylate [42]. However, the ylide retarded the polymerization of N-vinylpyrrolidone, initiated by AIBN at 60°C in benzene [44]. (See also Table 2.)... 

Since this pioneering work a number of IPNs have been prepared. Poly(styrene) has been used as the second network polymer in conjunction with several other polymers, including poly(ethyl acrylate), poly(n-butyl acrylate), styrene-butadiene, and castor oil. Polyurethanes have been used to form IPNs with poly(methyl methacrylate), other acrylic polymers, and with epoxy resins. 

Two free radical-initiated polymerizations are used in turn as examples the homopolymerization of methyl methaK rylate and the copolymerization of styrene n-butyl methacrylate. 

Figure 9 shows the result of injecting 10 gA of the total low molecular weight fraction from GPC 1 (Column Code A2) into GPC 2 (Column Code Bl). With this column code, GPC 2 is performing as a High Performance Liquid Chromatograph (HPLC). Separation is based upon solubility (i.e. composition differences) rather than upon molecular size. Methyl methacrylate monomer was used as a reference and added to the solution injected into GPC 1. Concentrations of n-butyl methacrylate, styrene and conversion are readily calculated from the peak areas and initial concentrations. 

In highly acidic environments a reaction product of an isobutyraldehyde and an alkylene amine compound with an alkylsulfopropionic amide group is recommended [1888,1889]. The alkylene amine compound can be the product of a reaction of equimolar amounts of N-dodecylmercaptan, methyl methacrylate, and diethylenetriamine. 

Triphenylmethane leuco dyes are used for photographic materials. The photographic system requires a polymer binder such as acrylic acid-methyl methacrylate copolymer115 or a copolymer of isophthalic and terephthalic acids116 a sensitizer such as 4-(4-n-amyloxyphenyl)-2,6-bis(3-ethylphenyl)-thiapyrilium perchlorate,117 a photo initiator such as hexaarylbisimi-dazole,118 and phenyl tribromomethyl sulfone, cycloalkane such as 1,2,3, 4,5-pentabromo-6-chlorocyclohexane,119 or 3-benzylidene-9-methyl-2,3-dihydro- 1 TZ-cyclopenta [b] quinoline.120... 

Materials. Methyl methacrylate was a product of Rohm and Haas, and t-butyl methacrylate was obtained from Polvsciences, Inc. Potassium trimethylsilanolate (PTMS) was obtained from Petrarch Systems, Inc. Anhydrous lithium iodide, trimethylsilyl iodide (TMSI), and n-butyllit.ium (in hexanes) were purchased from Aldrich Chemical Co. 

A copolymer of tri-n-butyltin methacrylate (TBTM) and methyl methacrylate (MMA), which is the active agent in antifouling... 

Syntheses. Isotactic poly(methyl methacrylate) was synthesized by the method of Tsuruta et al. (9 ). Under a nitrogen atmosphere, a quantity of 6 mL (0.056 mole) of methyl methacrylate (MMA) dried over 4A molecular sieve was dissolved in 24 mL of similarly dried toluene. To the glass vial containing the reaction was added 0.65 mL of 1.6 M n-butyllithium, and the reaction was kept at -78°C in a dry ice/isopropanol bath. The polymerization was halted 24 hr later with the addition of hydrochloric acid and methanol (methanol/water 4.1 by volume). The polymer was dried in vacuo at 50°C, redissolved in methylene chloride, precipitated by being poured into water-containing methanol, and dried in vacuo at 50°C. Tacticlty and composition were verified with % NMR. Yield 47%. 

Atactic poly(methyl methacrylate/methacrylic acid), the copolymer of methyl methacrylate (MMA) and methacrylic acid (MAA), was synthesized "directly" as a prepolymer to be esterified with bis(tri-n-butyltin) oxide (TBTO). Two formulations of poly (MMA/MAA) were synthesized, a 1 1 and a 2 1 MMA and MAA copolymer whose syntheses differ only in the proportion of monomer reacted. 

In a second method, a 1 g sample of poly(tri-n-butyltin methacrylate/methyl methacrylate) was dissolved in 4 mL of chloroform. One mL of concentrated HC1 was added dropwise with shaking until no more precipitate appeared. The precipitate was removed and then shaken again with a clean batch of chloroform and HC1. 

A free-radical synthesis of poly(tri-n-butyltin methacrylate/methyl methacrylate) was also carried out by the DTNSRDC chemists. 

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