Effect of Polymerization on the Swelling Properties of a Sodium Bentonite and its Mechanism

2020 ◽  
Vol 1003 ◽  
pp. 228-232
Author(s):  
Ji Xiang Nie ◽  
Ryoga Tanaka ◽  
Jin Chun Chai
Keyword(s):  
Free Radical ◽  
Deionized Water ◽  
Polymer Chains ◽  
Nacl Solution ◽  
X Ray Diffraction ◽  
Swelling Properties ◽  
Sodium Bentonite ◽  
X Ray ◽  
Free Swelling ◽  
Polymerization Method

The effect of polymerization on the swelling properties of a sodium bentonite has been investigated experimentally using free swelling index (FSI). Using free radical polymerization method in cationic solution with acrylate acid as the monomer (M) and potassium persulfate as initiator (I), the optimum conditons for higher FSI value in 0.6 M NaCl solution were pH of 5.5 and I/M ratio of 0.005. The polymerized bentonite (PB) had much higher FSI values than that of untreated bentonite (UB) in deionized water and 0.6 M NaCl solution. However, in the 0.6 M CaCl2 solution, the FSI value of PB was slightly lower than that of UB and the reason is not clear yet. The X-ray diffraction (XRD) test shows that polymer chains did not enter the interlayer of sodium bentonite crystals and it is postulated that the polymers only wrapped around the particles of the bentonite.

scholarly journals Isomeric 4,2′:6′,4″- and 3,2′:6′,3″-Terpyridines with Isomeric 4′-Trifluoromethylphenyl Substituents: Effects on the Assembly of Coordination Polymers with [Cu(hfacac)2] (Hhfacac = Hexafluoropentane-2,4-dione)

Inorganics ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 54
Author(s):  
Giacomo Manfroni ◽  
Simona S. Capomolla ◽  
Alessandro Prescimone ◽  
Edwin C. Constable ◽  
Catherine E. Housecroft
Keyword(s):  
Coordination Polymers ◽  
Metal Binding ◽  
Polymer Chains ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
Preparative Scale ◽  
X Ray ◽  
Single Crystal Structures ◽  
Π Stacking ◽  
Packing Interactions

The isomers 4′-(4-(trifluoromethyl)phenyl)-4,2′:6′,4″-terpyridine (1), 4′-(3-(trifluoromethyl)phenyl)-4,2′:6′,4″-terpyridine (2), 4′-(4-(trifluoromethyl)phenyl)-3,2′:6′,3″-terpyridine (3), and 4′-(3-(trifluoromethyl)phenyl)-3,2′:6′,3″-terpyridine (4) have been prepared and characterized. The single crystal structures of 1 and 2 were determined. The 1D-polymers [Cu2(hfacac)4(1)2]n.2nC6H4Cl2 (Hhfacac = 1,1,1,5,5,5-hexafluoropentane-2,4-dione), [Cu(hfacac)2(2)]n.2nC6H5Me, [Cu2(hfacac)4(3)2]n.nC6H4Cl2, [Cu2(hfacac)4(3)2]n.nC6H5Cl, and [Cu(hfacac)2(4)]n.nC6H5Cl have been formed by reactions of 1, 2, 3 and 4 with [Cu(hfacac)2].H2O under conditions of crystal growth by layering and four of these coordination polymers have been formed on a preparative scale. [Cu2(hfacac)4(1)2]n.2nC6H4Cl2 and [Cu(hfacac)2(2)]n.2nC6H5Me are zig-zag chains and the different substitution position of the CF3 group in 1 and 2 does not affect this motif. Packing of the polymer chains is governed mainly by C–F...F–C contacts, and there are no inter-polymer π-stacking interactions. The conformation of the 3,2′:6′,3″-tpy unit in [Cu2(hfacac)4(3)2]n.nC6H4Cl2 and [Cu(hfacac)2(4)]n.nC6H5Cl differs, leading to different structural motifs in the 1D-polymer backbones. In [Cu(hfacac)2(4)]n.nC6H5Cl, the peripheral 3-CF3C6H4 unit is accommodated in a pocket between two {Cu(hfacac)2} units and engages in four C–Hphenyl...F–Chfacac contacts which lock the phenylpyridine unit in a near planar conformation. In [Cu2(hfacac)4(3)2]n.nC6H4Cl2 and [Cu(hfacac)2(4)]n.nC6H5Cl, π-stacking interactions between 4′-trifluoromethylphenyl-3,2′:6′,3″-tpy domains are key packing interactions, and this contrasts with the packing of polymers incorporating 1 and 2. We use powder X-ray diffraction to demonstrate that the assemblies of the coordination polymers are reproducible, and that a switch from a 4,2′:6′,4″- to 3,2′:6′,3″-tpy metal-binding unit is accompanied by a change from dominant C–F...F–C and C–F...H–C contacts to π-stacking of arene domains between ligands 3 or 4.

scholarly journals Adsorption of malic acid at the hydroxyapatite/aqueous NaCl solution interface

2021 ◽  
Author(s):  
Władysław Janusz ◽  
Ewa Skwarek
Keyword(s):  
Zeta Potential ◽  
Malic Acid ◽  
Particle Sizes ◽  
Nacl Solution ◽  
X Ray Diffraction ◽  
Radioisotope Method ◽  
X Ray ◽  
Solution Interface ◽  
Adsorption Desorption ◽  
Kinetics Of

AbstractThe aim of the study was the basic incidence on the phenomenon of adsorption that occurs at the hydroxyapatite/malic acid interface, leading to a change in the surface properties of hydroxyapatite, Analytical methods used in the research: X-ray diffraction (XRD) as well as by the, adsorption–desorption of nitrogen (ASAP), potentiometric titration. The specific adsorption of malic acid ions at the hydroxyapatite interface was investigated by means of the radioisotope method. The zeta potential of hydroxyapatite dispersions was determined by electrophoresis with Zetasizer Nano ZS90 by Malvern. The particle sizes of hydroxyapatite samples were analyzed using Masteriszer 2000 Malvern. Studies on the kinetics of malic acid on hydroxyapatite from a solution with an initial concentration of 1 mmol/dm3 have shown that the adsorption process is initially fast, followed by a slow adsorption step. An increase in the pH of the solution causes a decrease in the malic acid adsorption as a result of competition with hydroxyl ions. The presence of adsorbed malic acid was confirmed by the FTIR measurements. The effect of malic acid adsorption on the zeta potential and particle size distribution of hydroxyapatite in the NaCl solution was investigated.

Synthesis, Structural, Morphological and I-V Characteristics of Polyaniline-MgCl Composite

2022 ◽  
Vol 1048 ◽  
pp. 141-146
Author(s):  
Madihally Nagaraja ◽  
Geetha Thippeswamy ◽  
Sushma Prashanth ◽  
Jayadev Pattar ◽  
Mahesh Hampapatna Mahesh
Keyword(s):  
Structural Analysis ◽  
Oxidative Polymerization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sem Micrographs ◽  
Morphological Studies ◽  
Current Voltage ◽  
Amorphous Nature ◽  
Diffraction Patterns ◽  
Polymerization Method

Composite of polyaniline-MgCl has been synthesized using oxidative polymerization method. Synthesized samples were characterized for structural analysis using FTIR and XRD. Morphological studies were carried by SEM micrographs. Current-Voltage (I-V) properties are obtained through Kiethly source meter. FTIR spectrum of polyaniline-MgCl composite indicates all the characteristic peaks of polyaniline. X-ray diffraction patterns represented the amorphous nature of polyaniline-MgCl composite. SEM micrographs confirmed the presence of MgCl particles in polyaniline matrix. I-V characteristics have shown the ohmic type behavior of polyaniline and polyaniline-MgCl composite.

Simulations of High-Strain Electrostrictive Chlorinated Terpolymers

2003 ◽  
Vol 785 ◽  
Author(s):  
George J. Kavarnos ◽  
Thomas Ramotowski
Keyword(s):  
Vinylidene Fluoride ◽  
High Strain ◽  
Polymer Chains ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lamellar Structures ◽  
Annealing Conditions ◽  
Poly Vinylidene Fluoride ◽  
Electromechanical Responses ◽  
Kinetics Of

ABSTRACTChlorinated poly(vinylidene fluoride/trifluoroethylene) terpolymers are remarkable examples of high strain electrostrictive materials. These polymers are synthesized by copolymerizing vinylidene fluoride and trifluoroethylene with small levels of a third chlorinated monomer. The electromechanical responses of these materials are believed to originate from the chlorine atom, which, by its presence in the polymer chains and by virtue of its large van der Waals radius, destroys the long-range crystalline polar macro-domains and transforms the polymer from a normal to a high-strain relaxor ferroelectric. To exploit the strain properties of the terpolymer, it is desirable to understand the structural implications resulting from the presence of the chlorinated monomer. To this end, computations have been performed on model superlattices of terpolymers using quantum-mechanical based force fields. The focus has been on determining the energetics and kinetics of crystallization of the various polymorphs that have been identified by x-ray diffraction and fourier transform infrared spectroscopy. The chlorinated monomer is shown to act as a defect that can be incorporated into the lamellar structures of annealed terpolymer without a high cost in energy. The degree of incorporation of the chlorinated monomer into the crystal lattice is controlled by annealing conditions and ultimately determines the ferroelectric behavior of the terpolymers.

scholarly journals Copper Containing Glass-Based Bone Adhesives for Orthopaedic Applications: Glass Characterization and Advanced Mechanical Evaluation

2020 ◽  
Author(s):  
Sahar. Mokhtari ◽  
Anthony.W. Wren
Keyword(s):  
Mechanical Properties ◽  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Viscoelastic Behavior ◽  
Polymer Chains ◽  
Nano Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compression Data

AbstractThis study addresses issues with currently used bone adhesives, by producing novel glass based skeletal adhesives through modification of the base glass composition to include copper (Cu) and by characterizing each glass with respect to structural changes. Bioactive glasses have found applications in fields such as orthopedics and dentistry, where they have been utilized for the restoration of bone and teeth. The present work outlines the formation of flexible organic-inorganic polyacrylic acid (PAA) – glass hybrids, commercial forms are known as glass ionomer cements (GICs). Initial stages of this research will involve characterization of the Cu-glasses, significant to evaluate the properties of the resulting adhesives. Scanning electron microscopy (SEM) of annealed Cu glasses indicates the presence of partial crystallization in the glass. The structural analysis of the glass using Raman suggests the formation of CuO nanocrystals on the surface. X-ray diffraction (XRD) pattern and X-ray photoelectron spectroscopy (XPS) further confirmed the formation of crystalline CuO phases on the surface of the annealed Cu-glass. The setting reaction was studied using Fourier transform infrared spectroscopy (ATR-FTIR). The mechanical properties of the Cu containing adhesives exhibited gel viscoelastic behavior and enhanced mechanical properties when compared to the control composition. Compression data indicated the Cu glass adhesives were efficient at energy dissipation due to the reversible interactions between CuO nano particles and PAA polymer chains.

scholarly journals A microstructural and corrosion resistance study of (Zr, Si, Ti)N-Ni coatings produced through co-sputtering

DYNA ◽  
2018 ◽  
Vol 85 (207) ◽  
pp. 192-197 ◽  
Author(s):  
Estrella Natali Borja-Goyeneche ◽  
Jhon Jairo Olaya-Florez
Keyword(s):  
Corrosion Resistance ◽  
Nickel Content ◽  
Corrosion Current ◽  
Nacl Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
X Ray Scattering ◽  
Current Densities ◽  
Fcc Phase

This work researches the influence of the nickel content on the structural and anticorrosive properties of ZrSiTiN films deposited by means of reactive co-sputtering on alloys of Ti6Al4V. The morphology and structure were analyzed by means of scanning electron microscopy (SEM) and X-ray diffraction (XRD), and the chemical composition was identified via X-ray scattering spectroscopy (EDS). The corrosion resistance was studied using potentiodynamic polarization (PP) tests employing a 3.5% by weight NaCl solution. In the films, an increase of Ni up to 6.97 at% was observed, while in XRD the FCC phase of (Zr, Ti) N was identified, with a mixed orientation in planes (111) and (200), which tended to diminish with the increase of Ni. Finally, with the addition of Ni, the corrosion current densities were reduced from 5.56 𝑥 10−8 to 2.64 𝑥 10−9 𝐴/𝑐m2. The improvement in the corrosion resistance is due to the effect of the Ni on the microstructure of the system (Zr, Ti) N, which can improve the quality of the passive film and prevent crystalline defects and corrosion zones.

Microstructural and Corrosion Studies by Immersion in 3.5% NaCl Solution on Aged Mg-9Al-1Zn-XCa Alloy

2019 ◽  
Vol 969 ◽  
pp. 93-97
Author(s):  
S. Manivannan ◽  
B. Narenthiran ◽  
A. Sivanantham ◽  
S.P. Kumaresh Babu
Keyword(s):  
Corrosion Behaviour ◽  
Nacl Solution ◽  
X Ray Diffraction ◽  
Corrosion Attack ◽  
X Ray ◽  
Α Phase ◽  
Corrosion Studies ◽  
Different Temperatures ◽  
Xrd Techniques ◽  
Scanning Electron

The experimatal alloys were aged at different temperatures of 180°C, 200°C, 220°C, and 240º C with calcium addition levels of (X=0.5, 1, 1.5, 2%) on Mg-6Al-1Zn-XCa alloy were investigated in 3.5% NaCl solution. All the experimatal alloys were immersed in 3.5% NaCl solutions and the resulted surface were analyzed to study the corrosion behaviour and its surface topography by optical microscopy (OM), scanning electron microscopy (SEM), energy dispersed spectroscopy (EDS) and X-ray diffraction (XRD) techniques. The result shows that corrosion attack occurred predominantly on ß phase and α phase exhibit relatively minor corrosion. In addition to that the increased aging temperature coarsens the intermetallic as well as α- Mg grains, which shows adverse effect to corrosion resistances and the best result were obtained at composition of 0.5wt.% Ca aged at 200°C.

Characterization of electrospun polylactide nanofibers modified via atom transfer radical polymerization

2020 ◽  
pp. 152808372093038 ◽  
Author(s):  
Muhammad Mushtaq ◽  
Rahim Jindani ◽  
Amjad Farooq ◽  
Xin Li ◽  
Hina Saba ◽  
...  
Keyword(s):  
Atom Transfer Radical Polymerization ◽  
Radical Polymerization ◽  
Photoelectron Spectroscopy ◽  
Polymer Chains ◽  
Surface Grafting ◽  
Atom Transfer ◽  
X Ray ◽  
Polymerization Method ◽  
Scanning Electron

Polylactic acid-based membranes received considerable attention due to its novel biocompatibility, renewability, and biodegradability. In this study, PLA electrospun nanofibrous membrane was prepared and 2-dimethylaminoethyl methacrylate (DMAEMA) was used as a monomer for surface grafting of polymer chains via the atom transfer radical polymerization method. Then the PLA nanofibers were quaternized by using bromoethane. The characterization of poly(DMAEMA) graft PLA nanofiber (poly(DMAEMA)-g-PLA) membranes was done by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and energy dispersive X-ray spectroscopy. The results showed that the diameter of PLA nanofibers increased 15% as the concentration increased from 10% to 12% and then increased 23% as the concentration of PLA solution increased from 10% to 15%. But the regularity of average diameters is best achieved at 12% concentration.

Bioinspired synthesis of self-assembled calcium phosphate nanocomposites using block copolymer-peptide conjugates

2008 ◽  
Vol 23 (12) ◽  
pp. 3196-3212 ◽  
Author(s):  
Yusuf Yusufoglu ◽  
Yanyan Hu ◽  
Mathumai Kanapathipillai ◽  
Matthew Kramer ◽  
Yunus E. Kalay ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Calcium Phosphate ◽  
Small Angle ◽  
Polymer Chains ◽  
X Ray Diffraction ◽  
X Ray ◽  
Self Assembling ◽  
Transmission Electron ◽  
Angle Scattering ◽  
Inorganic Content

Thermoreversibly gelling block copolymers conjugated to hydroxyapatite-nucleating peptides were used to template the growth of inorganic calcium phosphate in aqueous solutions. Nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), transmission electron microscopy, x-ray diffraction, and small-angle scattering were used to characterize these samples and confirm that the peptides promoted the growth of hydroxyapatite as the inorganic phase. Three different polymer templates were used with varying charges on the polymer chains (nonionic, anionic, and zwitterionic), to investigate the role of charge on mineralization. All of the polymer-inorganic solutions exhibited thermoreversible gelation above room temperature. Nanocomposite formation was confirmed by solid-state NMR, and several methods identified the inorganic component as hydroxyapatite. Small angle x-ray scattering and electron microscopy showed thin, elongated crystallites. Thermogravimetric analysis showed an inorganic content of 30–45 wt% (based on the mass of the dried gel at ∼200 °C) in the various samples. Our work offers routes for bioinspired bottom-up approaches for the development of novel, self-assembling, injectable nanocomposite biomaterials for potential orthopedic applications.

A New Method to Produce Superfine and Nano-Sized Fe Powders: Spark Plasma Discharge Process

2007 ◽  
Vol 561-565 ◽  
pp. 861-863 ◽  
Author(s):  
Chang Chun Ge ◽  
Jun Yu ◽  
Wei Ping Shen ◽  
Cheng Cheng ◽  
Guo Hua Ni ◽  
...  
Keyword(s):  
Single Phase ◽  
Spherical Shape ◽  
Plasma Discharge ◽  
Deionized Water ◽  
High Yield ◽  
Discharge Process ◽  
X Ray Diffraction ◽  
Bimodal Size Distribution ◽  
X Ray ◽  
Spark Plasma

Superfine and nano-sized Fe powders were prepared by a spark plasma discharge process in deionized water. The powders were characterized by Field Emission Scanning Electron Microscope (FESEM) with Oxford Inca EDX, and X-ray diffraction (XRD). The experimental results indicate that the powders prepared by the process have a bimodal size distribution, high purity, single phase, good spherical shape and high yield.

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