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Ethyl acrylate random

DPD 6169 Ethylene-ethyl acrylate random copolymer Union Carbide Co. [Pg.151]

Styrene/ethyl acrylate random copolymers were prepared with ethyl acrylate..contents of 10,25,50,75 and 90% by weight. Examination of the 3C NMR spectra of the copolymers reveals that the carbonyl carbon of the acrylate ester is a sensitive probe of the sequence distribution in these copolymers. Figure 2 shows the carbonyl carbon resonance region for a sample containing 50%... [Pg.388]

Figure 9 shows the results obtained for a DSC study of the variation of the Tg and transition temperatures for a series of styrene-ethyl acrylate random copolymers. The reader is referred to the literature for details about the synthesis of this copolymer series. This study was the first of its kind to characterize both the Tg and Tn transitions for a series of random copolymers over the entire composition range. Both the glass transition and the Tn transition showed a linear temperature dependence with copolymer composition. The TulTg ratio, where the transition temperatures are expressed in degrees Kelvin, averaged 1.2 for the four intermediate random copolymers. [Pg.196]

Fig. 9. Effect of copolymer composition on the and Tn transitions for a series of styrene-ethyl acrylate random copolymers. The TulTg ratio averaged 1.2 over the entire composition range. After Kumler et al., ref. 28. Fig. 9. Effect of copolymer composition on the and Tn transitions for a series of styrene-ethyl acrylate random copolymers. The TulTg ratio averaged 1.2 over the entire composition range. After Kumler et al., ref. 28.
Experimental determinations of the contributions above those predicted by the reference phantom network model have been controversial. Experiments of Rennar and Oppermann [45] on end-linked PDMS networks, indicate that contributions from trapped entanglements are significant for low degrees of endlinking but are not important when the network chains are shorter. Experimental results of Erman et al. [46] on randomly cross-linked poly(ethyl acrylate)... [Pg.350]

Polyisobutylene (Butyl Rubber, Copolymer with 0.5-2% Isoprene) (HR) Chloro-Sulfonated Polyethylene (CSM) Ethylene-Propylene Random Copolymer, 50% Ethylene (EPM) Ethylene-Propylene Random Terpolymer 50% Ethylene (EPDM) Poly(Ethyl Acrylate), Usually a Copolymer (ACM) Vinylidene-Fluoride-Chlorotrifluoro Ethylene Random Copolymer (FKM) Vinylidene— Fluoride— Hexafluoropropylene Random Copolymer (FKM)... [Pg.863]

Figure 3. HPLC-chromatogram of styrene-ethyl acrylate copolymers at different compositions and high conversion. Also shown is the styrene content obtained by HPLC calibration -) and on-line HPLC- H NMR experiments (o). (Reprinted from MacromolChem.Phys, Vol.201, LKramer, W.HiUer, H. On-line coupling of gradient-HPLC and NMR for the analysis of random poly[(styrene)-co-(ethyl acrylate)]s , 1662-1666, 2001, with permission from Wiley-VCH)... Figure 3. HPLC-chromatogram of styrene-ethyl acrylate copolymers at different compositions and high conversion. Also shown is the styrene content obtained by HPLC calibration -) and on-line HPLC- H NMR experiments (o). (Reprinted from MacromolChem.Phys, Vol.201, LKramer, W.HiUer, H. On-line coupling of gradient-HPLC and NMR for the analysis of random poly[(styrene)-co-(ethyl acrylate)]s , 1662-1666, 2001, with permission from Wiley-VCH)...
Elastomers are generally crosslinked in a random manner and therefore it is difficult to obtain the quantitative, independent information (molecular weight M, between crosslinks, functionality (p of the network) required to test the molecular theories. However, some systems such as natural rubber cured by dicumyl peroxide >, irradiated polymers " or even chemically randomly crosslinked polydimethyl-siloxane and poly(ethyl acrylate) have been investigated. Mark has exploit ... [Pg.141]

H random copolymer 55/45 ethyl acrylate/methyl methacrylate... [Pg.227]

Problem 11.5 Devise a synthetic scheme, using TEiMPO-based SFRP, to obtain graft copolymers of controlled molecular weight and low polydispersity, in which random copolymers of styrene (St) and ethyl acrylate (EA) containing about 0.2 mole fraction of ELA are grafted onto polystyrene (PS) chains. [Pg.588]

Scheme Pll.5.1 Graft copolymer synthesis random copolymer of styrene and ethyl acrylate grafted onto polystyrene (Problem 11.5). (Drawn following the synthesis method of Hawker, 1995.)... Scheme Pll.5.1 Graft copolymer synthesis random copolymer of styrene and ethyl acrylate grafted onto polystyrene (Problem 11.5). (Drawn following the synthesis method of Hawker, 1995.)...
Koppers Company produced SMA-type molding powders under the trade name of Dylark but this business was acquired by Arco which continues to produce these SMA type products. Monsanto has extended the SMA terpolymer investigation to Include random copolymers and alternating copolymers in which the copolymers with SMA are acrylonitrile, ethyl acrylate, Isobutylene, methyl acrylate, and methyl methacrylate (20). These terpolymers (S/MA/X) and rubber modified Cadon have created an entire new family of engineering polymers (21). New patents have been issued for both glassy terpolymers and rubber modified S/MA/AN (22, 23). As might be expected, the incompatable blends are characterized by two glass transition temperatures (Tg) (24). [Pg.132]

FIGURE 5.4 Chromatograms of poly (styrene—co ethyl acrylatels of different chemical composition. Source Reprinted from D. Braun, I. Kramer, H. Pasch, S. Mori, Phase separation in random copolymers from high conversion free radical polymerization. Part 2. Chemical heterogeneity analysis of poly(styrene-co-ethyl acrylate) by gradient HPLC., Macromolecular Chemistry and Physics, 200 (1999) 949, (1999), used with permission from Wiley-VCH (Ref [29]). [Pg.102]

Figure 3, i.e., 50/50-styrene/ethyl acrylate copolymer made by uniform (random), staged, or power feed processes (24). Using the carbonyl carbon of the acrylate ester as a probe of the sequence distributions in a series of random styrene/ethyl acrylate copolymer, assignments were made for the three major resonance regions in terms of triad sequences. Figure 6 illustrates the differences observed. In the... [Pg.229]

Coupled HPLC-NMR measurements performed at slow flow rates in fully deuterated solvents and at room temperature have been made in several studies to determine polymer MWD, to analyze the end-groups and the copolymer chemical composition distribution, and to assess the chemical structure and the degree of polymerization of all oligomer species [176-178]. Gradient HPLC-NMR was used in the analysis of the chemical composition distribution of random poly (styrene-co-ethyl acrylate) copolymers [179]. A major drawback in most of these studies is that the measurements could only be conducted at ambient or slightly elevated temperatures, which limits the method applicability, since many polymers, such as polyethylene, polypropylene, and polyolefin copolymers are soluble at high temperatures. [Pg.219]

Kramer I, Hiller W, Pasch H. On-line coupling of gradient-HPLC and IH NMR for the analysis of random poly[(styrene)-co-(ethyl acrylate)]s. Macromol Chem Phys 2000 201 1662-1666. [Pg.227]

A DMTA study of polyolefin-clay nanocomposites has shown that alpha, beta and gamma relaxations of the polymer were affected by polymer chain branching and clay exfoliation level [50]. Salmeron Sanchez and co-workers [51] studied the structure of the system obtained after free radical copolymerisation of ethyl acrylate and hydroxyethyl methacrylate comonomers using dynamic-mechanical and calorimetric techniques. Copolymerisation theory states that the free radical copolymerisation reaction of two monomers may give rise to a copolymer with a different chain composition from that of the random mixture corresponding to the original solution. In this system, the dynamic-mechanical spectra suggested there were two main alpha relaxation processes in the copolymers. [Pg.128]

In another example, polyarylate (PAR) end-capped by a COOH group was melt reacted with a random terpolymer of ethylene, ethyl acrylate and glycidyl methacrylate (E-EA-GMA), the extent of the interfacial reaction being controlled by the addition of various amounts of stearic acid that consumed part of the epoxy groups. The minor phase (E-EA-GMA) was first compounded, and the phase inversion that occurred upon the addition of the major phase (PAR) was delayed as less stearic acid was added [73]. [Pg.106]

The early hot melt adhesives were not strictly definable as rubber-based adhesives. Most rubber polymers such as natural rubber and random SBR are of such molecular weight and structure that they do not melt readily to a workable coating consistency at a temperature below which thermal degradation and decomposition take place. Certain synthetic polymers, however, lend themselves to the formulation of a wide range of hot melt adhesive compositions. Polyamide and polyester resins, ethylene-vinyl acetate (EVA) copolymers, ethylene-ethyl acrylate (EEA) copolymers, low molecular weight polyethylene and amorphous polypropylene, and certain vinyl ethers have found application in hot melt adhesives. These adhesives have found wide use in packaging, industrial, and construction applications. [Pg.561]


See other pages where Ethyl acrylate random is mentioned: [Pg.506]    [Pg.506]    [Pg.70]    [Pg.184]    [Pg.390]    [Pg.328]    [Pg.2534]    [Pg.49]    [Pg.1032]    [Pg.14]    [Pg.338]    [Pg.340]    [Pg.238]    [Pg.214]    [Pg.220]    [Pg.42]    [Pg.579]    [Pg.156]    [Pg.393]    [Pg.231]    [Pg.104]   
See also in sourсe #XX -- [ Pg.391 ]




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