scholarly journals In Situ Nitroxide-Mediated Polymerized Poly(acrylic acid) as a Stabilizer/Compatibilizer Carbon Nanotube/Polymer Composites

2007 ◽  
Vol 2007 ◽  
pp. 1-12 ◽  
Author(s):  
Vitaliy Datsyuk ◽  
Laurent Billon ◽  
Christelle Guerret-Piécourt ◽  
Sylvie Dagréou ◽  
Nicolas Passade-Boupatt ◽  
...  
Keyword(s):  
Carbon Nanotube ◽  
Acrylic Acid ◽  
Polymer Composites ◽  
Diblock Copolymers ◽  
Polymer Network ◽  
Electron Microscopies ◽  
Transmission Electron ◽  
Wide Range ◽  
Poly Acrylic Acid

Carbon nanotube (CNT) polymer composites were synthesized via in situ nitroxide-mediated diblock copolymerization. Poly(acrylic acid) (PAA) was chosen as a first block to obtain a precomposite CNT-PAA which is readily dispersible in various solvents including water. The immobilization of the stable poly(acrylic acid) alkoxyamine functionality on the nanotube surface occurs during the synthesis of the first block without CNT prior treatment. The living character of this block is established by spectroscopic methods and the nature of the CNT/PAA interaction is discussed. This living first block offers the opportunity to reinitiate the polymerization of a second block that can be chosen among a wide range of monomers. This versatility is illustrated with a second block containing methyl acrylate (MA) or styrene (S). Scanning and transmission electron microscopies confirm good CNT dispersion in the polymer network, while transmission electron microscopy also spots the anchorage locations of PAA on the CNT surface. Such nanotubes wrapped by diblock copolymers can be dispersed in various polymer matrices to create CNT—polymer composites. Conductivity measurements show that these composites obey a percolation-like power law with a low percolation threshold (less than 0.5 vol%) and a high maximum conductivity (up to 1.5 S/cm at room temperature).

Optimal response surface design of Gum tragacanth-based poly[(acrylic acid)-co-acrylamide] IPN hydrogel for the controlled release of the antihypertensive drug losartan potassium

RSC Advances ◽  
2014 ◽  
Vol 4 (75) ◽  
pp. 39822-39829 ◽  
Author(s):  
Saruchi Saruchi ◽  
B. S. Kaith ◽  
Rajeev Jindal ◽  
Vaneet Kumar ◽  
Manpreet S. Bhatti
Keyword(s):  
Controlled Release ◽  
Acrylic Acid ◽  
Polymer Network ◽  
Interpenetrating Polymer Network ◽  
Losartan Potassium ◽  
Surface Design ◽  
Gum Tragacanth ◽  
Ph Conditions ◽  
Poly Acrylic Acid

The present study proposes the development and optimization of a new interpenetrating polymer network (IPN), consisting of Gum tragacanth, poly(acrylic acid) (PAA), and poly(acrylamide) (PAAm), for the in situ controlled release of losartan potassium under different pH conditions at 37 °C.

Immobilization of urease in poly(1-vinyl imidazole)/poly(acrylic acid) network

2010 ◽  
Vol 64 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Mehmet Şenel ◽  
Agah Coşkun ◽  
M. Fatih Abasıyanık ◽  
Ayhan Bozkurt
Keyword(s):  
Acrylic Acid ◽  
Enzyme Immobilization ◽  
Storage Stability ◽  
Polymer Network ◽  
Ft Ir ◽  
Basic Characteristics ◽  
And Storage ◽  
Menten Constant ◽  
Ft Ir Spectroscopy ◽  
Poly Acrylic Acid

AbstractIn this study, urease was immobilized in a polymer network obtained by complexation of poly(1-vinyl imidazole) (PVI) with poly(acrylic acid) (PAA). Preparation of the polymer network was monitored by FT-IR spectroscopy. Scanning electron microscopy (SEM) revealed that enzyme immobilization had a strong effect on film morphology. Proton conductivity of the PVI/PAA network was measured via impedance spectroscopy under humidified conditions. Values of the Michaelis-Menten constant (K M) for immobilized urease were higher than for the free enzyme, indicating a decreased affinity of the enzyme to its substrate. The basic characteristics (pHopt, pHstability, T opt, T stability, reusability, and storage stability) of immobilized urease were determined. The results show that the PAA/PVI polymer network is suitable for enzyme immobilization.

scholarly journals Formation and Stability of Smooth Thin Films with Soft Microgels Made of Poly(N-Isopropylacrylamide) and Poly(Acrylic Acid)

Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2638
Author(s):  
Elena Buratti ◽  
Ilaria Sanzari ◽  
Franco Dinelli ◽  
Themistoklis Prodromakis ◽  
Monica Bertoldo
Keyword(s):  
Acrylic Acid ◽  
Colloidal Particles ◽  
Polymer Network ◽  
Spin Speed ◽  
Glass Substrates ◽  
Smooth Film ◽  
The Difference ◽  
The Stability ◽  
Individual Particles ◽  
Poly Acrylic Acid

In this work, soft microgels of Poly(N-Isopropylacrylamide) (PNIPAm) at two different sizes and of interpenetrated polymer network (IPN) composed of PNIPAm and Poly(Acrylic Acid) (PAAc) were synthesized. Then, solutions of these different types of microgels have been spin-coated on glass substrates with different degrees of hydrophobicity. PNIPAm particles with a larger diameter form either patches or a continuous layer, where individual particles are still distinct, depending on the dispersion concentration and spin speed. On the other, PNIPAm particles with a smaller diameter and IPN particles form a continuous and smooth film, with a thickness depending on the dispersion concentration and spin-speed. The difference in morphology observed can be explained if one considers that the microgels may behave as colloidal particles or macromolecules, depending on their size and composition. Additionally, the microgel size and composition can also affect the stability of the depositions when rinsed in water. In particular, we find that the smooth and continuous films show a stimuli-dependent stability on parameters such as temperature and pH, while large particle layers are stable under any condition except on hydrophilic glass by washing at 50 °C.

scholarly journals The Anomalous Influence of Polyelectrolyte Concentration on the Deposition and Nanostructure of Poly(ethyleneimine)/Poly(acrylic acid) Multilayers

Molecules ◽  
2019 ◽  
Vol 24 (11) ◽  
pp. 2141 ◽  
Author(s):  
Martin Müller
Keyword(s):  
Acrylic Acid ◽  
Attenuated Total Reflection ◽  
Silicon Substrates ◽  
Acid Base ◽  
Exponential Relationship ◽  
Individual Adsorption ◽  
The Individual ◽  
Poly Acrylic Acid

The deposition and nanostructure of polyelectrolyte (PEL) multilayers (PEMs) of branched poly(ethyleneimine)/poly(acrylic acid) (PEI/PAA) onto silicon substrates was studied in terms of the dependence of pH and the PEL concentration (cPEL) in the individual adsorption steps z. Both a commercial automatic dipping device and a homebuilt automatic stream coating device (flow cell) were used. Gravimetry, SFM, transmission (TRANS) and in situ attenuated total reflection (ATR) FTIR spectroscopy were used for the quantitative determination of the adsorbed amount, thickness, chemical composition and morphology of deposited PEMs, respectively. Firstly, the combination of pH = 10 for PEI and pH = 4 for PAA, where both PEL were predominantly in the neutral state, resulted in an extraordinarily high PEM deposition, while pH combinations, where one PEL component was charged, resulted in a significantly lower PEM deposition. This was attributed to both PEL conformation effects and acid/base interactions between basic PEI and acidic PAA. Secondly, for that pH combination an exponential relationship between PEM thickness and adsorption step z was found. Thirdly, based on the results of three independent methods, the course of the deposited amount of a PEM-10 (z = 10) versus cPEL in the range 0.001 to 0.015 M at pH = 10/4 was non-monotonous showing a pronounced maximum at cPEL = 0.005 M. Analogously, for cPEL = 0.005 M a maximum of roughness and structure size was found. Fourthly, related to that finding, in situ ATR-FTIR measurements gave evidence for the release of outermost located PEI upon PAA immersion (even step) and of outermost PAA upon PEI immersion (odd step) under formation of PEL complexes in solution. These studies help us to prepare PEL-based films with a defined thickness and morphology for interaction with biofluids in the biomedical and food fields.

scholarly journals Sample Preparation Methodologies for In Situ Liquid and Gaseous Cell Analytical Transmission Electron Microscopy of Electropolished Specimens

2016 ◽  
Vol 22 (6) ◽  
pp. 1350-1359 ◽  
Author(s):  
Xiang Li Zhong ◽  
Sibylle Schilling ◽  
Nestor J. Zaluzec ◽  
M. Grace Burke
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Focused Ion Beam ◽  
General Procedure ◽  
Ion Beam ◽  
Metals And Alloys ◽  
Stainless Steel Sample ◽  
Transmission Electron ◽  
Wide Range

AbstractIn recent years, an increasing number of studies utilizing in situ liquid and/or gaseous cell scanning/transmission electron microscopy (S/TEM) have been reported. Because of the difficulty in the preparation of suitable specimens, these environmental S/TEM studies have been generally limited to studies of nanoscale structured materials such as nanoparticles, nanowires, or sputtered thin films. In this paper, we present two methodologies which have been developed to facilitate the preparation of electron-transparent samples from conventional bulk metals and alloys for in situ liquid/gaseous cell S/TEM experiments. These methods take advantage of combining sequential electrochemical jet polishing followed by focused ion beam extraction techniques to create large electron-transparent areas for site-specific observation. As an example, we illustrate the application of this methodology for the preparation of in situ specimens from a cold-rolled Type 304 austenitic stainless steel sample, which was subsequently examined in both 1 atm of air as well as fully immersed in a H2O environment in the S/TEM followed by hyperspectral imaging. These preparation techniques can be successfully applied as a general procedure for a wide range of metals and alloys, and are suitable for a variety of in situ analytical S/TEM studies in both aqueous and gaseous environments.

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