Optical Characterisation of Non-Covalent Interactions between Non-Conjugated Polymers and Chemically Converted Graphene

2014 ◽  
Vol 67 (1) ◽  
pp. 168 ◽  
Author(s):  
Yufei Wang ◽  
Xueliang Hou ◽  
Chi Cheng ◽  
Ling Qiu ◽  
Xuehua Zhang ◽  
...  

Optical characterisation using dye molecules as probes was used to study the non-covalent interactions between chemically converted graphene (CCG) and non-conjugated, water soluble polymers in aqueous solution. The strong adsorption of non-conjugated polymers such as poly(ethylene oxide) (PEO) and poly(vinyl alcohol) (PVA) on CCG is observed by fluorescence and ultraviolet-visible spectroscopy and atomic force microscopy, and this leads to desorption of π-conjugated molecules from CCG. Such adsorption/desorption behaviour can be tailored by modifying the molecular weight of polymers and the chemistry of graphene. This finding provides a facile and non-covalent approach to the functionalisation of CCG and opens up new opportunities for the fabrication of graphene/polymer nanocomposites.

1999 ◽  
Vol 72 (2) ◽  
pp. 308-317 ◽  
Author(s):  
Siby Varghese ◽  
Yosuke Katsumura ◽  
Keizo Makuuchi ◽  
Fumio Yoshi

Abstract Technological properties of radiation vulcanized latex after mixing with water soluble polymers (WSP) such as poly(vinyl alcohol), poly(ethylene oxide) etc. have been studied in detail. The properties of water soluble polymer incorporated vulcanizates depend mainly on the type of the polymer blended into the latex. Most of the polymers showed a drastic increase in tear strength with polymer content and a reduction in tackiness of the vulcanized films. Radiation processing increases the water soluble protein content in the serum phase whereas that in the rubber phase decreases. Addition of water soluble polymer causes the fast leaching of soluble proteins from the dried films, which reduces the prolonged leaching commonly adopted for rubber vulcanizates. Aging properties of radiation vulcanized films incorporated with water soluble polymers are excellent. The thermal degradation behavior of radiation vulcanized films and that of water soluble polymer incorporated films is almost the same. Transparency of the rubber films can be increased by the addition of suitable water soluble polymers.


2011 ◽  
Vol 2 (4) ◽  
pp. 131-148 ◽  
Author(s):  
Francis Vidya ◽  
Subin S. Raghul ◽  
Sarita G Bhat ◽  
Eby Thomas Thachil

The main objective of this study was to enhance the rate of UV and biodegradation of polyethylene by incorporating biodegradable materials and prooxidants. Prooxidants such as transition metal complexes are capable of initiating photooxidation and polymer chain cleavage, rendering the product more susceptible to biodegradation. In this work, the effect of (1) a metallic photoinitiator, cobalt stearate, and (2) different combinations of cobalt stearate and vegetable oil on the photooxidative degradation of linear low-density poly(ethylene)-poly(vinyl alcohol) (LLDPE/PVA) blend films has been investigated. For this, film-grade LLDPE was blended with different proportions of PVA. PVA is widely used in the industrial field, and recently it has attracted increasing attention as a water-soluble biodegradable polymer. Cobalt stearate and vegetable oil were added to the blends as prooxidants. The blends were prepared by melt mixing in a Thermo HAAKE Polylab system. Thin films containing these additives were prepared by a subsequent compression moulding process. The effect of UV exposure on LLDPE/PVA films in the presence as well as absence of these additives was investigated. Tensile properties, FTIR spectra, and scanning electron microscopy (SEM) were employed to investigate the degradation behaviour. It was found


Nanoscale ◽  
2017 ◽  
Vol 9 (48) ◽  
pp. 19191-19200 ◽  
Author(s):  
Jinglin Shen ◽  
Zhi Wang ◽  
Di Sun ◽  
Guokui Liu ◽  
Shiling Yuan ◽  
...  

Supramolecular self-assembly, based on non-covalent interactions, has been employed as an efficient approach to obtain various functional materials from nanometer-sized building blocks, in particular, [Ag6(mna)6]6−, mna = mercaptonicotinate (Ag6-NC).


2020 ◽  
Vol 7 (3) ◽  
pp. 248-255
Author(s):  
Ludmila Matienko ◽  
Mil Elena Mickhailovna ◽  
Binyukov Vladimir Ivanovich ◽  
Goloshchapov Alexandr Nikolaevich

Background: In this study, we show that the AFM method not only allows monitoring the morphological changes in biological structures fixed on the surface due to H-bonds, but also makes it possible to study the self-organization of metal complexes by simulating the active center of enzymes due to intermolecular H-bonds into stable nanostructures; the sizes of which are much smaller than the studied biological objects. The possible role of intermolecular hydrogen bonds in the formation of stable supramolecular metal complexes, which are effective catalysts for the oxidation of alkyl arenes to hydroperoxides by molecular oxygen and mimic the selective active sites of enzymes, was first studied by AFM. Methods and Results: The formation of supramolecular structures due to intermolecular hydrogen bonds and, possibly, other non-covalent interactions, based on homogenous catalysts and models of active centers enzymes, heteroligand nickel and iron complexes, was proven by AFM-technique. AFM studies of supramolecular structures were carried out using NSG30 cantilever with a radius of curvature of 2 nm, in the tapping mode. To form nanostructures on the surface of a hydrophobic, chemically modified silicon surface as a substrate, the sample was prepared using a spin-coating process from solutions of the nickel and iron complexes. The composition and the structure of the complex Ni2(acac)(OAc)3·NMP·2H2O were determined in earlier works using various methods: mass spectrometry, UV- and IR-spectroscopy, elemental analysis, and polarography. Self-assembly of supramolecular structures is due to intermolecular interactions with a certain coordination of these interactions, which may be a consequence of the properties of the components themselves, the participation of hydrogen bonds and other non-covalent interactions, as well as the balance of the interaction of these components with the surface. Using AFM, approaches have been developed for fixing on the surface and quantifying parameters of cells. Conclusion: This study summarizes the authors' achievements in using the atomic force microscopy (AFM) method to study the role of intermolecular hydrogen bonds (and other non-covalent interactions) and supramolecular structures in the mechanisms of catalysis. The data obtained from AFM based on nickel and iron complexes, which are effective catalysts and models of active sites of enzymes, indicate a high probability of the formation of supramolecular structures in real conditions of catalytic oxidation, and can bring us closer to understanding enzymes activity. With a sensitive AFM method, it is possible to observe the self-organization of model systems into stable nanostructures due to H-bonds and possibly other non-covalent interactions, which can be considered as a step towards modeling the active sites of enzymes. Methodical approaches of atomic force microscopy for the study of morphological changes of cells have been developed.


Nanomaterials ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 52 ◽  
Author(s):  
Martin Wortmann ◽  
Natalie Frese ◽  
Lilia Sabantina ◽  
Richard Petkau ◽  
Franziska Kinzel ◽  
...  

Electrospinning is a new technology whose scope is gradually being developed. For this reason, the number of known polymer–solvent combinations for electrospinning is still very low despite the enormous variety of substances that are potentially available. In particular, electrospinning from low-toxic solvents, such as the use of dimethyl sulfoxide (DMSO) in medical technology, is rare in the relevant scientific literature. Therefore, we present in this work a series of new polymers that are applicable for electrospinning from DMSO. From a wide range of synthetic polymers tested, poly(vinyl alcohol) (PVOH), poly(2ethyl2oxazolene) (PEOZ), and poly(vinylpyrrolidone) (PVP) as water-soluble polymers and poly(styrene-co-acrylonitrile) (SAN), poly(vinyl alcohol-co-ethylene) (EVOH), and acrylonitrile butadiene styrene (ABS) as water-insoluble polymers were found to be suitable for the production of nanofibers. Furthermore, the influence of acetone as a volatile solvent additive in DMSO on the fiber morphology of these polymers was investigated. Analyses of the fiber morphology by helium ion microscopy (HIM) showed significantly different fiber diameters for different polymers and a reduction in beads and branches with increasing acetone content.


1978 ◽  
Vol 173 (2) ◽  
pp. 569-578 ◽  
Author(s):  
T Marshall ◽  
A Allen

1. A high-molecular-weight glycoprotein constitutes over 80% by weight of the total glycoprotein from water-soluble pig colonic mucus. 2. It was isolated from from nucleic acid and non-covalently bound protein by nuclease digestion followed by equilibrium centrifugation in a CsCl gradient. 3. The glycoprotein has the following composition by weight: fucose 10.4%; glucosamine 23.9%; galactosamine 8.3%; sialic acid 9.9%; galactose 20.8%; sulphate 3.0%; protein 13.3%; moisture about 10%. 4. The native glycoprotein has the high mol.wt. of 15×10(6). 5. Reduction of the native glycoprotein with 2-mercaptoethanol results in a glycoprotein of mol.wt. 6×10(6). 6. Pronase digestion removes 29% of the protein (3% of the glycoprotein) but none of the carbohydrate. 7. The molecular weight of the Pronase-digested glycoprotein is 1.5×10(6), which is halved to 0.76×10(6) on reduction with 2-mercaptoethanol. 8. The contribution of non-covalent interactions, disulphide bridges and the non-glycosylated peptide core to the quaternary structure of the glycoprotein are discussed and compared with the known structure of pig gastric glycoportein.


1992 ◽  
Vol 7 (9) ◽  
pp. 2599-2611 ◽  
Author(s):  
Phillip B. Messersmith ◽  
Samuel I. Stupp

We report here on the synthesis of new materials termed organoceramics in which polymers are molecularly dispersed within inorganic crystalline phases. These nanocomposite materials may not only have unique morphologies and physical properties but may also lead to new processing methods for ceramic-based materials. In organoceramics polymer molecules could opportunistically occupy sites such as grain boundaries or other two-dimensional defects, nanopores, lattice channels, or interlamellar spaces. Our synthetic approach to get macromolecules to those sites is to nucleate and grow inorganic crystals from homogeneous solutions containing the polymer chains as co-solutes. The new materials discussed in this manuscript were synthesized by growing calcium aluminate crystals in the presence of water soluble polymers and were characterized by x-ray diffraction, scanning electron microscopy, elemental analysis, and diffuse reflectance infrared spectroscopy. The macromolecules used in organoceramic synthesis included poly(vinyl alcohol), poly(dimethyldiallyl ammonium chloride), and poly(dibutyl ammonium iodide). We found that the chemistry of polymer repeats can impact on the spatial distribution of the dispersed organic chains and also on the morphology of organoceramic powders. In the case of the poly(vinyl alcohol) organoceramic the polymer is intercalated in “flattened” conformations in Ca2Al(OH)6[X] ·nH2O, thus increasing the distance between ionic layers from 7.9 Å to ∊ 18 Å (X is a monovalent or divalent anion). Such a layered nanocomposite can be formed only by intercalating the poly(vinyl alcohol) during growth of the Ca2Al(OH)6[X] · nH2O crystal. The synthetic pathway is therefore able to overcome large entropic barriers and incorporate significant amounts of polymer in the organoceramic product, in some cases up to 38% by weight. The particles of this nanocomposite are spheroidal aggregates of thin plate crystals whereas the use of a polycationic polymer in the synthesis leads to rod-like particles in which organic chains may reside in channels of the inorganic crystal.


RSC Advances ◽  
2015 ◽  
Vol 5 (39) ◽  
pp. 30555-30563 ◽  
Author(s):  
Siddheshwar B. Jagtap ◽  
Ramakant K. Kushwaha ◽  
Debdatta Ratna

Novel green method was developed to prepare nanocomposites of poly (ethylene oxide) (PEO) and graphene in water. This method is environment friendly with no health hazards and can be adapted to any other water soluble polymers.


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