181048
Poly(ethylene-co-acrylic acid)
acrylic acid 20 wt. %, beads
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About This Item
Linear Formula:
(CH2CH2)x[CH2CH(CO2H)]y
CAS Number:
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
InChI
1S/C3H4O2.C2H4/c1-2-3(4)5;1-2/h2H,1H2,(H,4,5);1-2H2
SMILES string
C=C.OC(=O)C=C
InChI key
QHZOMAXECYYXGP-UHFFFAOYSA-N
form
beads
composition
acrylic acid, 20 wt. %
density
0.96 g/mL at 25 °C
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Application
Processing and performance additive. Promotes crystallization of PET. Assists dispersion of additives in plastics.
Features and Benefits
Forms reversible ionic clusters (crosslinks). Promotes adhesion to various substrates, tougher, more chemically resistant and more transparent than parent acid copolymer.
signalword
Warning
hcodes
Hazard Classifications
Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>527.0 °F
flash_point_c
> 275 °C
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Ning Luo et al.
Colloids and surfaces. B, Biointerfaces, 50(2), 89-96 (2006-06-06)
Poly(ethylene-co-acrylic acid) (EAA) films were reacted with glycine, 12-aminododecanoic acid, aspartic acid, 5-aminoisophthalic acid, ethanolamine, diethylamine, dimethylamine, N-isopropylamine, and dimethylaminoethyleneamine to prepare EAA films with negatively charged, non-charged, hydrophilic, and hydrophobic functionalities. Attenuated total reflectance Fourier transform infrared spectroscopy, differential
Xiaodi Su et al.
Journal of colloid and interface science, 287(1), 35-42 (2005-05-26)
In this study, we use the quartz crystal microbalance with dissipation monitoring (QCM-D) to study the immobilization of the enzyme horseradish peroxidase (HRP) on poly(ethylene-co-acrylic acid) (PEAA) films. The surface polarity of spin-coated PEAA films was varied by heat treatments
Siri Schauff et al.
Analytical chemistry, 79(21), 8323-8326 (2007-10-09)
The separation process in reversed-phase high-performance liquid chromatography employing C18 phases is mainly due to hydrophobic interactions. The separation of tocopherol isomers, exhibited by the C30 phases, however, is additionally driven by shape selectivity. This phenomenon is investigated by suspended-state
Christoph Meyer et al.
Analytical and bioanalytical chemistry, 382(3), 679-690 (2004-08-04)
Three poly(ethylene-co-acrylic) acid copolymers (-CH(2)CH(2)-)(x)[CH(2)CH(CO(2)H)-](y) with different chain lengths and mass fractions of acrylic acid were covalently immobilized as stationary phases on silica via two variants of spacer molecules (3-aminopropyltriethoxysilane and 3-glycidoxypropyltrimethoxysilane). Different mobilities of the alkyl chains in the
Newton C Fawcett et al.
Langmuir : the ACS journal of surfaces and colloids, 20(16), 6651-6657 (2004-07-28)
Yoshimoto et al. [Anal. Chem. 2002, 74, 4306-4309] reported that a quartz crystal microbalance or QCM changed its response to sucrose solutions according to its angle of immersion. The effect was tentatively attributed to gravity-caused stress on the viscous interface
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