Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0267964 (
PAA
)
2,561
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Latexes are widely used for industrial applications, including decorative paints, binders for the papermaking industry, and drilling fluids for oil-field applications. In this work, the interest of capillary zone electrophoresis (CE) for the characterization of hydrophobic block copolymer latexes obtained by the conventional emulsion polymerization technique consisting of a core of polystyrene (PS) surrounded by a layer of poly(
ethyl acrylate
) (PEA) has been investigated. The PEA part of the copolymer can be partially hydrolyzed in poly(acrylic acid) (
PAA
) leading to PS-PEA-AA water-soluble amphiphilic copolymer having high viscosifying properties. The main purpose of this work was to evaluate the potential of CE for the characterization of the latexes at the different stages of the synthesis (PS core, PS-PEA diblock latex, and hydrolyzed PS-PEA-AA gel). The main analytical issues were to state (i) if there was free PS or PEA homopolymer latexes in the PS-PEA latex sample and (ii) if there was free PS, PEA, PS-PEA latexes, or free
PAA
chains in the PS-PEA-AA gel. Within this scope, this work describes the optimization of the selectivity of the separation between the different species (PS, PEA particles in the not hydrolyzed diblock latex and PS, PEA, PS-PEA particles as well as the polymer
PAA
chains in the PS-PEA-AA diblock gel sample obtained by latter latex hydrolysis). For that purpose, several experimental parameters were investigated such as pH and ionic strength of the background electrolyte (BGE) or the concentration of neutral surfactant added in the BGE. A challenging issue was to overcome the high viscosity of the PS-PEA-AA gel. This was resolved by the addition of 10 mM neutral surfactant in the gel sample and in the BGE. Finally, it is demonstrated that, within the detection limits, CE is a suitable analytical tool for controlling and monitoring the syntheses of these latexes and for intrinsically characterizing the distribution in charge density of the final PS-PEA-AA gel at different hydrolysis rates.
...
PMID:Characterization of copolymer latexes by capillary electrophoresis. 1987 76
pH sensitive graphene-polymer composites have been prepared by the modification of graphene basal planes with pyrene-terminated poly(2-N,N'-(dimethyl amino
ethyl acrylate
) (PDMAEA) and poly(acrylic acid) (
PAA
) via pi-pi stacking. The pyrene-terminal PDMAEA and
PAA
were synthesized using reversible addition-fragmentation chain transfer (RAFT) polymerization with a pyrene-functional RAFT agent. The graphene-polymer composites were found to demonstrate phase transfer behavior between aqueous and organic media at different pH values. Atomic force microscopy (AFM) analysis revealed that the thicknesses of the graphene-polymer sheets were approximately 3.0 nm when prepared using PDMAEA (M(n): 6800 and PDI: 1.12). The surface coverage of polymer chains on the graphene basal plane was calculated to be 5.3 x 10(-11) mol cm(-2) for PDMAEA and 1.3 x 10(-10) mol cm(-2) for
PAA
. The graphene-polymer composites were successfully characterized using X-ray photoelectron spectroscopy (XPS), attenuated total reflection infrared (ATR-IR) spectroscopy, and thermogravimetric analysis (TGA). Self-assembly of the two oppositely charged graphene-polymer composites afforded layer-by-layer (LbL) structures as evidenced by high-resolution scanning electron microscopy (SEM) and quartz crystal microbalance (QCM) measurements.
...
PMID:Synthesis, characterization, and multilayer assembly of pH sensitive graphene-polymer nanocomposites. 2042 64
Polymeric micelles based on light-responsive block copolymers were prepared and used for the phototunable detection of mercury(II) ions. 2-Nitrobenzyl acrylate (NBA) and ( E)-2-((4-((4-formylphenyl)diazenyl)phenyl)(methyl)amino)
ethyl acrylate
(FPDEA) were copolymerized from a poly(ethylene oxide) (PEO) macroinitiator via atom transfer radical polymerization (ATRP), leading to a well-defined block copolymer of PEO
113
- b-[p(NBA
10
- co-FPDEA
3
)] with a low polydispersity index (PDI = 1.16). After polymerization, the aldehyde groups of PEO- b-[p(NBA- co-FPDEA)] were converted to aldoxime groups by reacting with hydroxylamine, leading to the formation of a final oxime-containing polymeric probe, PEO- b-[p(NBA- co-HPDEA)], P1. The resulting block copolymer, P1, was self-assembled in water to yield spherical micelles that consist of a PEO block forming a hydrophilic shell and a copolymer of light-responsive NBA and a mercury(II) ion-detecting HPDEA block forming a hydrophobic core. Upon the addition of mercury(II) ions to this micellar solution, no detection was observed since water-soluble mercury(II) ions have limited accessability to the oxime units of P1, which are located in the hydrophobic core. After UV light irradiation, however, the photolabile 2-nitrobenzyl moieties were cleaved, and hydrophobic PNBA was transformed to hydrophilic poly(acrylic acid) (
PAA
), leading to the photoinduced dissociation of micelles to unimers. As a result, the oxime units of P1 were exposed to a hydrophilic environment and could react with mercury(II) ions to form nitrile groups, resulting in the turn-on detection of mercury(II) ions by UV light irradiation.
...
PMID:Polymeric Micelles Based on Light-Responsive Block Copolymers for the Phototunable Detection of Mercury(II) Ions Modulated by Morphological Changes. 3020 78
