scholarly journals Novel Hybrid Materials And Their Applications

2021 ◽  
Author(s):  
◽  
Aaron Charles Small

<p>The development of novel hybrid materials of cellulose fibres and substrates with nanoparticles, conducting polymers and quantum dots, opens up novel application for new packaging materials and paper based products for the ‘smart packaging’ and ‘functional products’ areas that are emerging in the paper and packaging industries. Examples of these materials which have been developed here include cellulose fibres and substrates functionalised with magnetic nanoparticles, electrically conducting polypyrrole, and photoluminescent zinc sulfide quantum dots.  Such materials were synthesised and then characterised using Alternating Gradient Magnetometry (AGM), Atomic Absorption Spectroscopy (AA), Cotec Profilometer Measurements, DC Conductivity Measurements, Photoluminescence Spectroscopy (PL), Scanning Electron Microscopy (SEM), SQUID Magnetometry, Transmission Electron Microscopy (TEM), Vibrational Sample Magnetometry (VSM), X-ray Diffraction (XRD), X-ray Fluorescence (XRF) and X-ray Photoelectron Spectroscopy (XPS).  Ferrimagnetic magnetite nanoparticles (particle size 12-26 nm) were synthesised by a simple aqueous precipitation method and had a magnetic saturation of approximately 60 emu g⁻¹, a coercive field of approximately 12-120 Oe, and a remnant magnetisation of approximately 11 emu g⁻¹.  Magnetite coated Kraft fibres (1.2 – 3.15 wt. % Fe) were synthesised by adding a colloidal suspension of magnetite nanoparticles to a suspension of Kraft fibres. The fibres retained their inherent properties, such as tensile strength and flexibility, but inherited the magnetic properties of the magnetic nanoparticles. The nanoparticles remained unchanged on bonding - presumably through hydrogen bonding between the surface hydroxyl groups of the cellulose and the oxygen present in the magnetite.  Newsprint, Kraft Board and Cotton fabric were coated with polypyrrole using a chemical polymerisation method. SEM shows a complete coating, whereby the fibres are completely encapsulated by the polymer, including individual fibrils. Again, bonding is facilitated through hydrogen bonding between the surface hydroxyl groups of the cellulose and the lone pairs of the nitrogen in the polypyrrole backbone. Samples were doped with p-toluenesulfonic acid to increase conductivity, of which up to 4 S cm⁻¹ was achieved.  The samples were coated with magnetite nanoparticles using a starch binder, and tested for their application in EMI shielding. A maximum shielding effectiveness of 43 % in the 1-18 GHz range and 47 % in the 16-40 GHz range was obtained using cotton fabrics coated with both polypyrrole and magnetite. A synergistic effect is observed on using a polypyrrole and magnetite coating.  Photoluminescent ZnS quantum dots, synthesised using an aqueous precipitation method, were doped with Mn²⁺ and Cu²⁺ to achieve emissions at approximately 600 nm (Mn²⁺) and 530 nm (Cu²⁺) on irradiation with UV light. The quantum dots had a particle size of approximately 2 nm, and were present in the zinc blende phase.  Doped ZnS-coated Kraft fibres (5 – 30 wt. % Zn) were synthesised by a number of methods, the most successful being the ‘in-situ’ method, in which a uniform and complete coating was afforded. The fibres retained their inherent properties, such as tensile strength and flexibility, but inherited the photoluminescent properties of the ZnS quantum dots. The quantum dots remained unchanged on bonding - presumably through hydrogen bonding between the surface hydroxyl groups of the cellulose and the sulfur present in the ZnS quantum dots.  ZnS quantum dots doped with Mn² and Cu²⁺ were successfully formulated for inkjet printing by capping with mercaptosuccinic acid. Upon irradiation with UV light, emissions at approximately 600 nm (Mn²⁺-doped) and 530 nm (Cu²⁺-doped) were observed. These were successfully inkjet printed in intricate patterns onto a number of substrates, including photographic quality inkjet paper, cotton, and wool.</p>

2021 ◽  
Author(s):  
◽  
Aaron Charles Small

<p>The development of novel hybrid materials of cellulose fibres and substrates with nanoparticles, conducting polymers and quantum dots, opens up novel application for new packaging materials and paper based products for the ‘smart packaging’ and ‘functional products’ areas that are emerging in the paper and packaging industries. Examples of these materials which have been developed here include cellulose fibres and substrates functionalised with magnetic nanoparticles, electrically conducting polypyrrole, and photoluminescent zinc sulfide quantum dots.  Such materials were synthesised and then characterised using Alternating Gradient Magnetometry (AGM), Atomic Absorption Spectroscopy (AA), Cotec Profilometer Measurements, DC Conductivity Measurements, Photoluminescence Spectroscopy (PL), Scanning Electron Microscopy (SEM), SQUID Magnetometry, Transmission Electron Microscopy (TEM), Vibrational Sample Magnetometry (VSM), X-ray Diffraction (XRD), X-ray Fluorescence (XRF) and X-ray Photoelectron Spectroscopy (XPS).  Ferrimagnetic magnetite nanoparticles (particle size 12-26 nm) were synthesised by a simple aqueous precipitation method and had a magnetic saturation of approximately 60 emu g⁻¹, a coercive field of approximately 12-120 Oe, and a remnant magnetisation of approximately 11 emu g⁻¹.  Magnetite coated Kraft fibres (1.2 – 3.15 wt. % Fe) were synthesised by adding a colloidal suspension of magnetite nanoparticles to a suspension of Kraft fibres. The fibres retained their inherent properties, such as tensile strength and flexibility, but inherited the magnetic properties of the magnetic nanoparticles. The nanoparticles remained unchanged on bonding - presumably through hydrogen bonding between the surface hydroxyl groups of the cellulose and the oxygen present in the magnetite.  Newsprint, Kraft Board and Cotton fabric were coated with polypyrrole using a chemical polymerisation method. SEM shows a complete coating, whereby the fibres are completely encapsulated by the polymer, including individual fibrils. Again, bonding is facilitated through hydrogen bonding between the surface hydroxyl groups of the cellulose and the lone pairs of the nitrogen in the polypyrrole backbone. Samples were doped with p-toluenesulfonic acid to increase conductivity, of which up to 4 S cm⁻¹ was achieved.  The samples were coated with magnetite nanoparticles using a starch binder, and tested for their application in EMI shielding. A maximum shielding effectiveness of 43 % in the 1-18 GHz range and 47 % in the 16-40 GHz range was obtained using cotton fabrics coated with both polypyrrole and magnetite. A synergistic effect is observed on using a polypyrrole and magnetite coating.  Photoluminescent ZnS quantum dots, synthesised using an aqueous precipitation method, were doped with Mn²⁺ and Cu²⁺ to achieve emissions at approximately 600 nm (Mn²⁺) and 530 nm (Cu²⁺) on irradiation with UV light. The quantum dots had a particle size of approximately 2 nm, and were present in the zinc blende phase.  Doped ZnS-coated Kraft fibres (5 – 30 wt. % Zn) were synthesised by a number of methods, the most successful being the ‘in-situ’ method, in which a uniform and complete coating was afforded. The fibres retained their inherent properties, such as tensile strength and flexibility, but inherited the photoluminescent properties of the ZnS quantum dots. The quantum dots remained unchanged on bonding - presumably through hydrogen bonding between the surface hydroxyl groups of the cellulose and the sulfur present in the ZnS quantum dots.  ZnS quantum dots doped with Mn² and Cu²⁺ were successfully formulated for inkjet printing by capping with mercaptosuccinic acid. Upon irradiation with UV light, emissions at approximately 600 nm (Mn²⁺-doped) and 530 nm (Cu²⁺-doped) were observed. These were successfully inkjet printed in intricate patterns onto a number of substrates, including photographic quality inkjet paper, cotton, and wool.</p>


Clay Minerals ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 537-546 ◽  
Author(s):  
J. E. F. C. Gardolinski ◽  
G. Lagaly

AbstractSeveral new interlayer-grafted derivatives of kaolinite were synthesized by esterification of inner-surface hydroxyl groups with alkanols, diols and glycol mono-ethers starting with the dimethyl sulphoxide intercalate. The derivatives were characterized by X-ray powder diffractometry, thermal analysis, Fourier transform infrared spectroscopy and transmission electron microscopy. The grafted molecules are arranged in monolayers between the kaolinite layers, with typical basal spacings of ~11.3 Å. Rheological studies of aqueous dispersions of the modified kaolinites revealed an exponential increase of the yield value and apparent viscosity with increasing alkyl chain length of the grafted molecules.


Clay Minerals ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 471-484 ◽  
Author(s):  
R. L. Frost ◽  
S. J. van der Gaast

AbstractRaman microscopy of the kaolinite polymorphs was used to study single crystals and bundles of aligned crystals of kaolinite. The spectra of the hydroxyl stretching region were both sample and orientation dependent. Kaolinites can be classified into two groups according to the ratio of the intensities of the 3685 and 3695 cm−1 bands. No relationship was found between the d-spacing and the crystal domain size measurement from the 001 reflection and the Raman spectral intensities indicating the Raman spectra are independent of d-spacing and crystallinity. However, a relationship of the crystallinity in the a-b direction and intensities of the 3685 and 3695 cm−1 bands indicate that the relative position of one layer to the other determines the position of the inner surface hydroxyl groups and the hydrogen bonding with the oxygen of the opposite layer. A new hypothesis based on symmetric and non-symmetric hydrogen bonding of the inner surface hydroxyl groups is proposed to explain the two inner surface hydroxyl bands centred at 3685 and 3695 cm−1. The bands at 3670 and 3650 cm−1 are described in terms of the out-of-phase vibrations of the in-phase vibrations at 3695 and 3685 cm−1.


1991 ◽  
Vol 222 ◽  
Author(s):  
Rika Sekine ◽  
Maki Kawai ◽  
Kiyotaka Asakura ◽  
Yasuhiro Iwasawa

ABSTRACTWe have already reported that copper and calcium dipivaloylmethanates [Cu(DPM)2 and Ca(DPM)2 ] reacts selectively and stoichiometrically with surface hydroxyl groups (OH) on SiO2. In order to clarify the structure of the adsorbed species and the origin of the reaction between M(DPM)2 (M=Cu and Ca) and OH groups, the surface adsorbed species are studied by infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), and the extended X-ray absorption fine structure (EXAFS). As a result, it was found that H from surface OH has moved into M(DPM)2 after the adsorption, where the four oxygen coordinated structure around Cu still exists in the adsorbed Cu(DPM)2. Introducing water vapor at 673 K to this surface results in the removal of ligand DPM from the adsorbed Cu(DPM)2. At 673 K, Cu atoms decomposed from the adsorbates aggregated on the surface. This fact supports that the interaction between the adsorbed Cu(DPM)2 and SiO2 surface is originated from that between the ligands and the surface.


1986 ◽  
Vol 51 (7) ◽  
pp. 1430-1438 ◽  
Author(s):  
Alena Reissová ◽  
Zdeněk Bastl ◽  
Martin Čapka

The title complexes have been obtained by functionalization of silica with cyclopentadienylsilanes of the type Rx(CH3)3 - xSi(CH2)nC5H5 (x = 1-3, n = 0, 1, 3), trimethylsilylation of free surface hydroxyl groups, transformation of the bonded cyclopentadienyl group to the cyclopentadienyl anion, followed by coordination of (h5-cyclopentadienyl)trichlorotitanium. The effects of single steps of the above immobilization on texture of the support, the number of free hydroxyl groups, the coverage of the surface by cyclopentadienyl groups and the degree of their utilization in anchoring the titanium complex have been investigated. ESCA study has shown that the above anchoring leads to formation of the silica-supported bis(h5-cyclopentadienyl)dichlorotitanium(IV) complex.


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