Acrylates copolymer
Rating : 6.5
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10 pts from FRanier
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"Acrylates copolymer studies" about Acrylates copolymer Review Consensus 10 by FRanier (9976 pt) | 2022-Apr-18 11:08 |
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Compendium of the most significant studies with reference to properties, intake, effects.
Peykova, Y., Lebedeva, O. V., Diethert, A., Müller-Buschbaum, P., & Willenbacher, N. (2012). Adhesive properties of acrylate copolymers: Effect of the nature of the substrate and copolymer functionality. International Journal of Adhesion and Adhesives, 34, 107-116.
Abstract. The adhesion performance of uncrosslinked and crosslinked butyl acrylate-methyl acrylate copolymers is compared.
Morita, M., Ogisu, H., & Kubo, M. (1999). Surface properties of perfluoroalkylethyl acrylate/n‐alkyl acrylate copolymers. Journal of Applied Polymer Science, 73(9), 1741-1749.
Abstract. Wetting behavior of perfluoroalkylethyl acrylate (FA)/n-alkyl acrylate (AA) copolymers with the various length of side chains of the AAs is discussed from a standpoint of surface molecular mobility. The copolymerization reactivity ratio indicates that these polymers are random copolymers. The surface properties were studied by measuring dynamic contact angle, static contact angle and freeze-dried X-ray photoelectron spectroscopy, and the bulk properties by wide-angle X-ray diffraction and differential scanning calorimetry.
Luo Q, Shi Z, Zhang Y, Chen XJ, Han SY, Baumgart T, Chenoweth DM, Park SJ. DNA Island Formation on Binary Block Copolymer Vesicles. J Am Chem Soc. 2016 Aug 17;138(32):10157-62. doi: 10.1021/jacs.6b04076.
Abstract. Here, we report DNA-induced polymer segregation and DNA island formation in binary block copolymer assemblies. A DNA diblock copolymer of polymethyl acrylate-block-DNA (PMA-b-DNA) and a triblock copolymer of poly(butadiene)-block-poly(ethylene oxide)-block-DNA (PBD-b-PEO-b-DNA) were synthesized, and each was coassembled with a prototypical amphiphilic polymer of poly(butadiene)-block-poly(ethylene oxide) (PBD-b-PEO).
Chroni A, Pispas S, Forys A, Trzebicka B. pH-Driven Morphological Diversity in Poly[n-Butyl Acrylate-block-(2-(Dimethylamino)Ethyl Acrylate)] Amphiphilic Copolymer Solutions. Macromol Rapid Commun. 2019 Dec;40(24):e1900477. doi: 10.1002/marc.201900477.
Abstract. Amphiphilic poly[n-butyl acrylate-block-(2-(dimethylamino)ethyl acrylate)] (PnBA-b-PDMAEA) block copolymers are synthesized by the reversible addition fragmentation chain transfer polymerization process. The pH-responsive self-assembly behavior in aqueous media is studied by dynamic, static, and electrophoretic light scattering and cryogenic transmission electron microscopy (Cryo-TEM) at different pHs.
Liu C, Yan B, Duan J, Hou B. Biofilm inhibition effect of an ivermectin/silyl acrylate copolymer coating and the colonization dynamics. Sci Total Environ. 2020 Sep 20;736:139599. doi: 10.1016/j.scitotenv.2020.139599.
Abstract. In this study, a coating was developed by mixing ivermectin with an acrylic-based resin, silyl acrylate copolymer, and a 45-day in situ antifouling test was conducted in the Yellow Sea.
Prüfert F, Hering U, Zaichik S, Le NN, Bernkop-Schnürch A. Synthesis and in vitro characterization of a preactivated thiolated acrylic acid/acrylamide-methylpropane sulfonic acid copolymer as a mucoadhesive sprayable polymer. Int J Pharm. 2020 Jun 15;583:119371. doi: 10.1016/j.ijpharm.2020.119371.
Abstract. Development of a preactivated thiomer as sprayable excipient for mucoadhesive formulations.
Gerding H. Fluorescein Staining of Intraocular Lenses. Klin Monbl Augenheilkd. 2018 Apr;235(4):369-372. English. doi: 10.1055/s-0043-124655.
Abstract. Recent case reports have indicated that intraocular lenses may be discoloured by systemically or locally applied fluorescein. Since very few data are available on the susceptibility of intraocular lenses to fluorescein, an experimental survey on lens discolouration was performed.
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"Descrizione" about Acrylates copolymer Review Consensus 10 by FRanier (9976 pt) | 2024-Oct-10 15:46 |
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Acrylates copolymer is a group of chemical compounds containing methacrylic and acrylic acid monomers or any of their salts or esters.
Acrylates Copolymer is a synthetic copolymer derived from the polymerization of acrylic acids and their derivatives. It is widely used in cosmetics and personal care products for its film-forming, emulsifying, and stabilizing properties. Due to its versatility, Acrylates Copolymer can be found in a broad range of formulations, including makeup products, hair care products, and skincare lotions.
Chemical Composition and Structure
Acrylates Copolymer is made from a combination of acrylic and methacrylic monomers, which form a polymer that can create a durable and flexible film on the surface of the skin or hair. Its polymer structure allows it to form waterproof films or improve the texture of a formulation, making products more stable and long-lasting.
Physical Properties
Acrylates Copolymer typically appears as a fine powder or viscous, colorless to whitish liquid, soluble in water or organic solvents depending on the formulation. It is valued for its ability to form transparent, durable films, which make cosmetic products longer-lasting and water-resistant—particularly useful in products like mascara, foundation, and sunscreens.
Production Process
The copolymer is produced through the polymerization of acrylic or methacrylic monomers, creating a polymer chain that can be modified to offer various properties such as elasticity or water resistance. The production process allows for tailoring the copolymer's characteristics to suit different cosmetic formulations.
The name defines the structure of the molecule:
The process of synthesis of acrylic copolymers takes place in several stages:
It appears as a milky liquid with good compatibility with polar solvents such as alcohol and good compatibility and synergistic thickening properties with anionic and non-ionic surfactants for polar solvent systems.
What they are used for and where
Cosmetics
Viscosity-enhancing and emulsion-stabilising agents with film-forming and fixation properties, fast-thickening binders.
Use:
Safety
Health and Safety Considerations
Safety in Use
Acrylates Copolymer is generally considered safe for use in cosmetics and personal care products. It is well-tolerated by the skin and is not known to cause irritation or sensitization when used at approved concentrations. However, consumers with particularly sensitive skin should perform a patch test before use.
Allergic Reactions
Allergic reactions to Acrylates Copolymer are rare, but as with any chemical ingredient, individuals with sensitive skin or a history of allergies should exercise caution when using products containing this ingredient.
Toxicity and Carcinogenicity
It has been studied for safety and is considered safe for use in cosmetics when used within the recommended concentrations. International regulations set concentration limits to ensure consumer safety.
Environmental and Safety Considerations
Acrylates Copolymer is a synthetic polymer, raising environmental concerns regarding its biodegradability. Although it does not pose an immediate environmental hazard, its long-term accumulation in ecosystems, especially aquatic systems, can be problematic. It is recommended to dispose of products containing this ingredient responsibly to reduce environmental impact.
Regulatory Status
Acrylates Copolymer is approved for use in cosmetics and personal care products by regulatory bodies such as the European Union and the Food and Drug Administration (FDA) in the United States. It is regulated to ensure safe use within specific concentration limits in cosmetic formulations.
Studies
The presence of residual monomers could be toxic if 2-ethylhexyl acrylate exceeds a concentration of 21% on the skin, however the "Final Report on the Safety Evaluation of Acrylate Copolymer and 33 Related Cosmetic Ingredients" concluded that "Although monomers may be toxic, the levels that would be found in cosmetic formulations are not considered a safety hazard. Consequently, these acrylate copolymers are considered safe for use in cosmetic formulations when formulated to avoid irritation." (1).
Appearance | Liquid |
Boiling Point | 99.5ºC at 760 mmHg |
pH | 4.0-7.0 |
Flash Point | 15.6ºC |
PSA | 89.90000 |
Vapor Pressure | 38.2mmHg at 25°C |
LogP | 2.11810 |
Storage | -20℃-30℃ |
Synonyms
References_________________________________________________________________________
(1) Zondlo Fiume M. Final report on the safety assessment of Acrylates Copolymer and 33 related cosmetic ingredients. Int J Toxicol. 2002;21 Suppl 3:1-50. doi: 10.1080/10915810290169800.
Abstract. Ingredients in the Acrylates Copolymer group all contain the monomers acrylic acid or methacrylic acid or one of their salts or esters. These ingredients are considered similar in that they are uniformly produced in chemical reactions that leave very little residual monomer. Although residual acrylic acid may be as high as 1500 ppm, typical levels are 10 to 1000 ppm. There is sufficient odor if residual monomers are present to cause producers to keep levels as low as possible. These ingredients function in cosmetics as binders, film formers, hair fixatives, suspending agents, viscosity-increasing agents, and emulsion stabilizers. Concentrations may be as high as 25% if used as a binder, film former, or fixative; or as low as 0.5% if used as a viscosity-increasing agent, suspending agent, or emulsion stabilizer. These very large polymers exhibit little toxicity. In rabbits and guinea pigs, Acrylates Copolymer did produce irritation, but no evidence of sensitization was found. The principle concern regarding the use of these polymer ingredients is the presence of toxic residual monomers. In particular, although 2-ethylhexyl acrylate was not genotoxic, it was carcinogenic when applied at a concentration of 21% to the skin of C3H mice. Lower concentrations (2.5%) and stop-dose studies at high concentrations (43%) were not carcinogenic. 2-Ethylhexyl acrylate was not carcinogenic in studies using NMRI mice. Whether an increase in carcinogenesis was seen or not, there was evidence of severe dermal irritation in these 2-ethylhexyl acrylate studies. Another concern regarding residual monomers was inhalation toxicity. Although the acrylic acid monomer is a nasal irritant, exposure to the monomer from use of these polymers in cosmetic formulations would always be less than the established occupational exposure limits for nasal irritation. Although there appears to be a huge variation in the mix of monomers used in the synthesis of these polymers, they are similar in that the polymers, except for dermal irritation, are not significantly toxic, and residual monomer levels are kept as low as possible. Although the monomers may be toxic, the levels that would be found in cosmetic formulations are not considered to present a safety risk. Accordingly, these Acrylate Copolymers are considered safe for use in cosmetic formulations when formulated to avoid irritation.
El-Sayed, S. M., Madani, M., & El-Bayoumi, A. S. (2009). Analytical calculations and properties of γ-rays polymerization of novel acrylates copolymer system. Physica B: Condensed Matter, 404(21), 4117-4124.
Abstract. A detailed study of some physical properties of pure PMMA (polymethyl methacrylate) film and MMA/Ani (methyl methacrylate/aniline) films is presented. Films of thicknesses ranged from 0.04 to 0.72 mm for MMA/Ani were prepared while it is 0.68 mm for PMMA. The structure of the sample is analyzed by X-ray diffraction technique and is found to be amorphous (PMMA) and partially crystalline (MMA/Ani). Ultra violet–visible electronic absorption spectra measurements were analyzed to obtain some important parameters such as molar extrication coefficient, oscillator strength, dipole strength and having good thermal stability (Td >300 °C) was also reported. TGA studies revealed that the thermal stability of polymethyl methacrylate, prepared by radiation polymerization of methyl methacrylate, improved after copolymerization with aniline. Also, optical behavior of film samples was analyzed by obtaining transmission spectra, in the wavelength range of 200–1100 nm. It was found that all studied samples lead to the appearance of a second edge at lower photon energy due to the formation of the induced energy states. From the intensity of absorption interband transitions (B and Q) which are assigned as type π–π* for both PMMA and MMA/Ani films, the energy gaps Eg1 and Eg2 were calculated respectively. The optical conductivity (σ) was determined and it was found that with the increase of thicknesses optical energy gap decreases monotonically and the refractive index increases.
Lin, J., Zheng, C., Zhu, M. N., Chen, Y. Z., Lu, P. P., Liu, Q., ... & Xu, C. L. (2015). Comparison of copolymer emulsions of fluorine and siloxane‐containing acrylates with core–shell structure for water‐repellent cotton fabrics coatings. Polymers for Advanced Technologies, 26(1), 68-76.
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