448672
Poly(ethylene-co-acrylic acid)
acrylic acid 15 wt. %
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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
composition
acrylic acid, 15 wt. %
hardness
≤15 dmm (ASTM D 5, 25 °C)
viscosity
600 cP(140 °C, Brookfield)(lit.)
acid number
112‑130 mg KOH/g
transition temp
Tm (DSC) 87 °C (at peak)
density
0.93 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.
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Marc David Grynbaum et al.
Journal of chromatography. A, 1156(1-2), 80-86 (2006-12-01)
The increased demand for chromatographic materials that are able to achieve a fast separation of large quantities of structure analogues is a great challenge. It is known that polymer based chromatographic materials have a higher loadability, compared to silica based
C Albano et al.
Journal of the mechanical behavior of biomedical materials, 4(3), 467-475 (2011-02-15)
In this investigation, the behavior of the mechanical properties of composites of high-density polyethylene/hydroxyapatite (HDPE/HA) with and without ethylene-acrylic acid copolymer (EAA) as possible compatibilizer, was studied. Different mathematical models were used to predict their Young's modulus, tensile strength and
Optician's occupational allergic contact dermatitis, paresthesia and paronychia caused by anaerobic acrylic sealants.
L Kanerva et al.
Contact dermatitis, 44(2), 117-119 (2001-02-24)
A P Martínez-Camacho et al.
Carbohydrate polymers, 91(2), 666-674 (2012-11-06)
The obtaining of chitosan extruded films was possible by using low density polyethylene (LDPE) as a matrix polymer and ethylene-acrylic acid copolymer as an adhesive, in order to ensure adhesion in the interphase of the immiscible polymers. The obtained blend
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
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