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CTBNs

Siebeif, A.R., Tolle, L.L. and Drake, R.S., CTBN-modified epoxies work in poor bonding conditions. Adhes. Age, 29, 19 (1986). [Pg.463]

Table B.8 Properties of CTBN-Expoxy Resin Compositions... Table B.8 Properties of CTBN-Expoxy Resin Compositions...
Composite Particles, Inc. reported the use of surface-modified rubber particles in formulations of thermoset systems, such as polyurethanes, polysulfides, and epoxies [95], The surface of the mbber was oxidized by a proprietary gas atmosphere, which leads to the formation of polar functional groups like —COOH and —OH, which in turn enhanced the dispersibility and bonding characteristics of mbber particles to other polar polymers. A composite containing 15% treated mbber particles per 85% polyurethane has physical properties similar to those of the pure polyurethane. Inclusion of surface-modified waste mbber in polyurethane matrix increases the coefficient of friction. This finds application in polyurethane tires and shoe soles. The treated mbber particles enhance the flexibility and impact resistance of polyester-based constmction materials [95]. Inclusion of treated waste mbber along with carboxyl terminated nitrile mbber (CTBN) in epoxy formulations increases the fracture toughness of the epoxy resins [96]. [Pg.1055]

CTBN type elastomers (carboxyl-terminated butadiene acrylonitrile) used to toughen this epoxy system. The Tg peak of the elastomer (-30°Q was shifted to higher temperatures suggesting that electron interaction resulted in crosslinking. The fact that the Tg peak disappeared at 10 rads suggests that crosslinking in the elastomer was extensive at high dose levels. [Pg.232]

Table VII summarizes the solubility parameters of MEK, the CTBN elastomers, and an epoxy resin of similar EEW. Table VII summarizes the solubility parameters of MEK, the CTBN elastomers, and an epoxy resin of similar EEW.
It is clear, that MEK is a "good" solvent for both the elastomers and the epoxy resin. Note that at 10% rubber, the MEK absorption nearly doubles. This implies that a much higher concentration of MEK is present in the rubber phase than in the epoxy phase. This is possible because the MEK diffuses more rapidly into the rubbery CTBN phase owing to its greater segmental thermal motion. [Pg.210]

Solvent absorption measurement has been shown to be a sensitive and useful test method in the manufacture of epoxy powder coatings. A test method was defined and the effects of time and temperature of immersion described. It was shown that solvent absorption is a measure of raw material properties (EEW of the epoxy resin, and CTBN elastomer type and concentration), the homogeneity of the extrudate, as well as the state of cure. The information obtained from solvent absorption measurements has proven to be extremely important not only in quality control analysis but also in providing an insight into the structure function relationships in epoxy resin chemistry. [Pg.210]

CTBN Carboxyl-Terminated Butadiene Acrylonitrile Rubber... [Pg.211]

Other papers reported the phase separation behavior for the composition showing dual phase morphology [7,20,21,43-45], Delides et al. [43] proposed that the viscosity at the point of phase separation is sufficiently large enough to inhibit diffusion of the epoxy through the rubber (CTBN) and result in the generation of the occluded phase, which is the inclusion of epoxy domains within the rubbery phase. [Pg.116]

Piperidine and carboxyl terminated butadiene acrylonitrile copolymer (CTBN) at 75 °C. [Pg.101]

The anhydride cured epoxies displayed a prominent carbonyl group of HHPA. The peak at 70 ppm was assigned to the products of the reacted epoxide groups. This peak was predominant in all four groups, piperidine-CTBN, MPDA, HHPA and NMA-DMBA. [Pg.101]

CTBN carboxyl-terminated butadiene-acrylonitrile rubber DETA diethylenetriamine... [Pg.46]


See other pages where CTBNs is mentioned: [Pg.7]    [Pg.31]    [Pg.31]    [Pg.189]    [Pg.443]    [Pg.173]    [Pg.200]    [Pg.246]    [Pg.250]    [Pg.221]    [Pg.286]    [Pg.293]    [Pg.330]    [Pg.338]    [Pg.348]    [Pg.374]    [Pg.173]    [Pg.195]    [Pg.199]    [Pg.200]    [Pg.207]    [Pg.207]    [Pg.210]    [Pg.113]    [Pg.135]    [Pg.195]    [Pg.195]    [Pg.196]    [Pg.196]    [Pg.101]    [Pg.80]    [Pg.81]   
See also in sourсe #XX -- [ Pg.33 ]




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Acrylonitrile copolymer), CTBN

Acrylonitrile copolymer), CTBN butadiene

Acrylonitrile copolymer), CTBN liquid carboxyl terminated

Butadiene-acrylonitrile copolymer) CTBN (liquid carboxyl

CTBN

CTBN

CTBN (carboxyl-terminated

CTBN (carboxyl-terminated butadiene

CTBN (liquid carboxyl terminated

CTBN (liquid carboxyl terminated butadiene-acrylonitrile

CTBN copolymers

CTBN polymers

CTBN rubbers

CTBN, carboxy-terminated

CTBN, epoxy toughness

CTBN, epoxy toughness Particle sizes

CTBN, epoxy toughness Structure

CTBN-epoxy adduct

CTBN-modified epoxy

CTBN-toughened epoxy resin

Carboxyl terminated acrylonitrile butadiene CTBN)

Carboxyl-terminated butadiene acrylonitrile CTBN) copolymer

Carboxyl-terminated butadiene-acrylonitrile elastomers CTBN)

DGEBA/CTBN

Epoxy/CTBN

Solid epoxy resins with CTBN

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