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Glycol dimethacrylate

Other constituents may be added to assist in the formation of uniform beads or to influence the use properties of the polymers through plasticization or cross-linking. These include lubricants, such as lauryl or cetyl alcohol and stearic acid, and cross-linking monomers such as di- or trivinylbenzene, diaHyl esters of dibasic acids, and glycol dimethacrylates. [Pg.170]

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. [Pg.233]

The DADC monomer has been copolymerized with small amounts of polyfunctional methacryflc or acryflc monomers. For example, 3% triethylene glycol dimethacrylate was used as a flexibiflzing, cross-linking agent with a percarbonate as initiator (26). CR-39 and diethylene glycol diacrylate containing isopropyl percarbonate were irradiated with a mercury lamp to a 92% conversion and then cured at 150°C (27). By a similar two-step process DADC was copolymerized with methyl methacrylate and tetraethylene glycol dimethacrylate (28). [Pg.83]

Third Monomers. In order to achieve certain property improvements, nitrile mbber producers add a third monomer to the emulsion polymerization process. When methacrylic acid is added to the polymer stmcture, a carboxylated nitrile mbber with greatly enhanced abrasion properties is achieved (9). Carboxylated nitrile mbber carries the ASTM designation of XNBR. Cross-linking monomers, eg, divinylbenzene or ethylene glycol dimethacrylate, produce precross-linked mbbers with low nerve and die swell. To avoid extraction losses of antioxidant as a result of contact with fluids duriag service, grades of NBR are available that have utilized a special third monomer that contains an antioxidant moiety (10). FiaaHy, terpolymers prepared from 1,3-butadiene, acrylonitrile, and isoprene are also commercially available. [Pg.522]

Dissolved in water and extracted with -heptane to remove ethylene glycol dimethacrylate (checked by gas-liquid chromatography and by NMR) and distilled twice under reduced pressure [Strop, Mikes and Kalal J Phys Chem 80 694 1 976]. [Pg.261]

The reluctance of acrylic monomers to polymerise in the presence of air has been made a virtue with the anaerobic acrylic adhesives. These are usually dimethacrylates such as tetramethylene glycol dimethacrylate. The monomers are supplied with a curing system comprising a peroxide and an amine as part of a one-part pack. When the adhesive is placed between mild steel surfaces air is excluded, which prevents air inhibition, and the iron present acts as a polymerisation promoter. The effectiveness as a promoter varies from one metal to another and it may be necessary to use a primer such as cobalt naphthenate. The anaerobic adhesives have been widely used for sealing nuts and bolts and for a variety of engineering purposes. Small tube containers are also available for domestic use. [Pg.420]

Mention may also be made here of a number of polyfunctional compounds such as allyl methacrylate and glycol dimethacrylates which have been used to produce a cross-linked sheet of enhanced heat resistance compared with conventional poly(methyl methacrylate). Some manufacturers supply the sheet in an incompletely cross-linked state which allows a limited amount of forming after which the sheet may be further heated to complete the cure. [Pg.423]

A process for the preparation of porous polyvinyl alcohol gels in three steps is (1) suspension polymerization of vinyl acetate with diethylene glycol dimethacrylate in the presence of a diluent as porogen, (2) saponifying of the resulting porous polyvinyl acetate gel with an alkali, and then (3) subjecting... [Pg.9]

EGDM-ethylene glycol dimethacrylate HQ-hydroquinone Mod(3)-300% Modulus. [Pg.469]

Glycol methacrylates (and retention times [RTs]) ethylene glycol dimethacrylate (RT = 13 min), diethyleneglycol dimethacrylate (RT = 18 min), triethylene glycol dimethacrylate (RT = 22 min), and tetraethylene glycol dimethacrylate... [Pg.62]

The y-radiation-induced grafting of diethylene glycol dimethacrylate and its mixture with (3-hydroxy ethyl methacrylate in ethanol-water systems onto silicone rubber has been reported [ 164]. The grafting yield increases as the radiation dose, concentration of monomer and concentration of transfer agent increase. At the same radiation dose, the degree of grafting decreases, as the dose level increases. However, at the same dose rate, the grafhng level increases with radiation dose. [Pg.871]

One of the calculation results for the bulk copolyroerization of methyl methacrylate and ethylene glycol dimethacrylate at 70 C is shown in Figure 4. Parameters used for these calculations are shown in Table 1. An empirical correlation of kinetic parameters which accounts for diffusion controlled reactions was estimated from the time-conversion curve which is shown in Figure 5. This kind of correlation is necessary even when one uses statistical methods after Flory and others in order to evaluate the primary chain length drift. [Pg.251]

In more complex forms of this resin hybrid, other dimethacrylates may be present, such as the ethylene glycol dimethacrylates, and bis-GMA, when HEMA acts as a co-solvent for water and bis-GMA (Antonucd, McKinney Stansbury, 1988). The general composition of these materials, which we term class I hybrids, is summarized below ... [Pg.170]

Other difunctional hydroxy dimethacrylates, e.g. the ethylene glycol dimethacrylates... [Pg.170]

OVS tube t-Butyl acrylate. Ethylene glycol-dimethacrylate... [Pg.197]

Ethylene glycol dimethacrylate EGDMA Elydrophobicity Wettability... [Pg.470]


See other pages where Glycol dimethacrylate is mentioned: [Pg.352]    [Pg.380]    [Pg.380]    [Pg.665]    [Pg.973]    [Pg.973]    [Pg.1016]    [Pg.1016]    [Pg.1016]    [Pg.243]    [Pg.268]    [Pg.427]    [Pg.427]    [Pg.427]    [Pg.229]    [Pg.104]    [Pg.472]    [Pg.839]    [Pg.1014]    [Pg.9]    [Pg.524]    [Pg.528]    [Pg.199]    [Pg.330]    [Pg.330]    [Pg.330]    [Pg.23]    [Pg.41]    [Pg.870]    [Pg.874]    [Pg.891]    [Pg.18]    [Pg.229]   
See also in sourсe #XX -- [ Pg.116 , Pg.117 , Pg.123 ]

See also in sourсe #XX -- [ Pg.48 ]




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DIMETHACRYLATE

Diethylene glycol dimethacrylate

Diethylene glycol dimethacrylate DEGDMA)

Dimethacrylates

Ethylene glycol dimethacrylate

Ethylene glycol dimethacrylate (EDMA

Ethylene glycol dimethacrylate (EGDMA

Ethylene glycol dimethacrylate Methyl

Ethylene glycol dimethacrylate crosslinking agent

Ethylene glycol dimethacrylate structure

Ethylene glycol dimethacrylate swelling

Ethylene glycol dimethacrylic acid

Ethylene glycole dimethacrylate (EGDMA

Methacrylic acid-ethylene glycol dimethacrylate

Methacrylic acid-ethylene glycol dimethacrylate MIPs

Methyl methacrylate-ethylene glycol dimethacrylate

Methyl methacrylate-ethylene glycol dimethacrylate copolymerization

Polyethylene glycol dimethacrylate

Polyethylene glycol dimethacrylate PEGDMA)

Tetraethylene glycol dimethacrylate

Triethylene glycol dimethacrylate

Triethylene glycol dimethacrylate TEDMA)

Triethylene glycol dimethacrylate TEGDMA)

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