Polyamide grafted with polypyrrole: formation, properties, and stability

2013 ◽  
Vol 67 (8) ◽  
Author(s):  
Katarína Mosnáčková ◽  
Mohamed Chehimi ◽  
Pavol Fedorko ◽  
Mária Omastová
Keyword(s):  
Photoelectron Spectroscopy ◽  
Surface Composition ◽  
Sol Gel ◽  
Attenuated Total Reflectance ◽  
Conducting Layer ◽  
Washing Process ◽  
Sol Gel Process ◽  
Pre Treatment ◽  
Surface Modified

AbstractConducting textiles of polyamide (PA) fabrics and polypyrrole (PPy) were prepared by in situ oxidative chemical polymerisation of pyrrole (Py) on the surface of PA textiles using FeCl3 as oxidant. The anionic surfactant, dodecylbenzenesulphonic acid, was used as co-dopant during Py polymerisation on the textile surface. The influence of the monomer amount and polymerisation conditions on formation of the conducting PPy layer, conductivity, morphology, and stability of the prepared PA/PPy was studied. The conductivity of modified textiles decreased rapidly after the washing process, so a special Py-functionalised silane (1-(3-(triethoxysilyl)propylamino)-3-(1-H-pyrrole-1-yl)propan-2-ol; SP) was synthesised and applied to the PA surface prior to PPy formation. The presence of SP on the PA surface after completion of the sol-gel process was verified by Fourier transform infrared spectroscopy with an attenuated total reflectance. Pyrrole polymerisation was subsequently applied to the SP pre-treated textile surface. The influence of SP concentration on both the fastness of the conducting layer after the washing process and stability of the electrical conductivity of the prepared PA/PPy samples was investigated. Surface conductivity of the samples treated and untreated by the sol-gel process of SP was measured both prior to and after washing of the prepared textiles. It was found that an application of 0.6 mass % of SP significantly improved the fastness of the PPy layers. Examination of the modified PA surface using scanning electron microscopy disclosed the differences in the formation of PPy on PA textiles when using SP and also showed differences on the PPy modified textile surface prior to and after washing. The method of X-ray photoelectron spectroscopy was used for a detailed study of the surface composition. It was confirmed that the pre-treatment with Py-functionalised triethoxysilane significantly influenced the chemical composition of the PA surface modified with PPy.

Synthesis and Intermolecularly Mediated Assembly of Organic Pigment in Hybrid Coating Films

1998 ◽  
Vol 519 ◽  
Author(s):  
Y. Yan ◽  
Z. Duan ◽  
D.-G. Chen ◽  
S. Ray Chaudhuri
Keyword(s):  
Sol Gel ◽  
Hybrid Coating ◽  
Hypsochromic Shift ◽  
Hybrid Films ◽  
Coating Films ◽  
Organic Pigment ◽  
Inorganic Hybrid ◽  
Matrix Interactions ◽  
Sol Gel Process

AbstractThe insoluble, strongly hydrogen bonded organic pigment of 3,6-bis-(4-chlorphenyl)-l,4- diketopyrrolo [3,4-c] pyrrole was transiently blocked by adding carbamate groups, and consequently incorporated into organic-inorganic hybrid matrices by a sol-gel process. The homo- (pigment-pigment) and hetero-intermolecular (pigment-matrix) interactions were found to control both the assembly and dispersion of pigment molecules in the hybrid coating films. A weaker interaction between matrices and pigment molecules results in aggregation of the carbamate pigment in the methyl-silicate films. A stronger interaction forms a homogenous dispersion and coloration of the phenyl-silicate films. The as-prepared methyl- and phenylsilicate films doped with the organic pigment were distinguished by a morphology change and a blue (hypsochromic) shift in absorption from 550 to 460 nm. Thermal treatment can remove the carbamate groups and in-situ form the organic pigment in the hybrid films.

Chemical Analyses of Sol/Gel Surfaces and Thin Films

1984 ◽  
Vol 32 ◽  
Author(s):  
Carlo G. Pantano ◽  
C. A. Houser ◽  
R. K. Brow
Keyword(s):  
Thin Films ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Silica Films ◽  
Alumina Films ◽  
Surface Analysis Techniques ◽  
Relative Water ◽  
Temperature Programmed

ABSTRACTThe application of surface analysis techniques to the characterization of sol/gel surfaces and thin films is described. Secondary-ion mass spectroscopy (SIMS), x-ray photoelectron spectroscopy (XPS) and sputter-induced photon spectroscopy (SIPS) are used to measure the composition of multicomponent silicate films, the relative water content of alumina films, the nitrogen content of ammonia treated silica films, and the depth profiles for films on black chrome. The determination of chemical structure using XPS and SIMS is also discussed. Finally, a brief introduction to temperature-programmed desorption (TPD) and its potential for studying surface chemical reactions, in situ, is presented.

Preparation of the polymerizable titania oriented to 3D printing and the laser-induced crystallization

2018 ◽  
Vol 24 (9) ◽  
pp. 1421-1427 ◽  
Author(s):  
Feng Liu ◽  
Shaoai Xie ◽  
Yan Wang ◽  
Jianjun Yu ◽  
Qinghua Meng
Keyword(s):  
3D Printing ◽  
Sol Gel ◽  
Crystal Form ◽  
Tetrabutyl Titanate ◽  
Content Type ◽  
Functional Additives ◽  
Sol Gel Process ◽  
Photosensitive Resin ◽  
Induced Crystallization

PurposeThe titania (titanium dioxide) is one of the important functional additives in the photosensitive resin and encounters the problem of stabilization in the photosensitive resin for 3D printing. This study aims to achieve enhancement in stabilization by preparation of the polymerizable titania andin situlaser-induced crystallization during 3D printing.Design/methodology/approachA type of polymerizable titania (AAEM@TiO2) was designed and prepared from tetrabutyl titanate (TBT) and 2-(acetoacetoxy)ethyl methacrylate (AAEM) via the sol–gel process, which was characterized by Fourier-transform infrared (FTIR) spectra, ultraviolet–visible (UV-Vis) spectra, surface bonding efficiency (SBE) and settling height (H). AAEM acted on both bonding to the titania and polymerization with the monomer in resin for stabilization. The polymerizable titania could be converted to the pigmented titania by means of laser-induced crystallization. The photosensitive resin was then formulated on the basis of optimization and used in a stereolithography apparatus (SLA) for 3D printing.FindingsThe stabilization effect of AAEM on TiO2was achieved and the mechanism of competition in the light-consuming reactions during photocuring was proposed. The ratio of nAAEM/nTBTin AAEM@TiO2, the concentration of AAEM@TiO2and photoinitiator (PI) used in the photosensitive resin were optimized. The anatase crystal form was indicated by X-ray diffraction (XRD) and clustering of nanocrystals was revealed by scanning electron microscopy (SEM) after SLA 3D printing.Originality/valueThis investigation provides a novel method of pigmentation by preparation of the polymerizable titania andin situlaser-induced crystallization for SLA 3D printing.

Epoxy resin modified with in situ generated metal oxides by means of sol-gel process

2011 ◽  
Vol 122 (3) ◽  
pp. 1792-1799 ◽  
Author(s):  
Federica Bondioli ◽  
Maria Elena Darecchio ◽  
Adrian S. Luyt ◽  
Massimo Messori
Keyword(s):  
Metal Oxides ◽  
Epoxy Resin ◽  
Sol Gel ◽  
Sol Gel Process

Photocatalytically Active Cotton Fabrics Produced with Anatase Synthesized Using a Low-Temperature Sol-Gel Process

2018 ◽  
Vol 762 ◽  
pp. 408-412
Author(s):  
Raivis Eglītis ◽  
Gundars Mežinskis
Keyword(s):  
Photocatalytic Activity ◽  
Uv Light ◽  
Sol Gel ◽  
Average Particle Size ◽  
Synthesis Method ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Sol Gel Process ◽  
Anatase Nanoparticles ◽  
Pre Treatment

In this work two different hydrosols were used to impregnate a commercially available cotton fabric with anatase nanoparticles to give it photocatalytic activity. To increase the activity, different pre-treatment methods were applied. The nanoparticle size was determined using dynamic light scattering and x-ray diffraction and the fabrics were examined using scanning electron microscopy. Photocatalytic activity was measured using the degradation of methyl-orange while irradiating the samples with UV light. The synthesis method allowed to produce anatase with an average particle size of 32 to 37 nm depending on the synthesis method used.

Antibacterial Activity of Surface-Modified Fabric with Ag/AgCl-Doped Quaternary Ammonium-Modified Silicate Hybrid

2019 ◽  
Vol 19 (11) ◽  
pp. 7285-7293 ◽  
Author(s):  
Kuo-Hui Wu ◽  
Yin-Chiung Chang ◽  
Ken-Fa Cheng ◽  
Je-Chuang Wang
Keyword(s):  
Colloidal Suspension ◽  
Sol Gel ◽  
Antimicrobial Properties ◽  
Woven Fabrics ◽  
Dipolar Interactions ◽  
Zone Of Inhibition ◽  
E Coli ◽  
Antibacterial Material ◽  
Surface Modified

An organic–inorganic hybrid antibacterial material based on Ag/AgCl and quaternary ammoniummodified silicate (Ormosil (NR+4 Cl-)) was prepared by sol–gel processes and an in situ reduction method, in which silver nitrate, tetraethoxysilane (TEOS), N-trimethoxysilylpropyl-N,N,Ntrimethylammonium chloride (TMAPS) and N-[3-(trimethoxysilyl)propyl]diethylenetriamine (ATS) acted as precursor, linker and colloidal suspension stabilizer, respectively. The physical properties of the Ormosil (NR+4 Cl-) and Ormosil (NR+4 Cl-)/Ag hybrids were examined using XPS and TGA spectroscopy, the results of which indicated that Ag/AgCl was immobilized in channels by dipolar interactions with the Ormosil (NR+4 Cl-) matrix. Ormosil (NR+4 Cl-) and Ormosil (NR+4 Cl-)/Ag sol solutions were used to functionalize non-woven fabrics by simply immersing the textiles into the dispersions in order to obtain antimicrobial fabrics. The antibacterial effects of the Ormosil/Ag- and Ormosil (NR+4 Cl-)/Ag-modified fabrics against Gram-negative P. aeruginosa and E. coli, and Grampositive S. aureus and B. subtilis, were assessed using the zone of inhibition and the plate-counting method. The antibacterial efficacy was maintained even after 20 laundry cycles. The results indicated that the Ormosil/Ag and Ormosil (NR+4 Cl-)/Ag hybrids are useful as non-leaching agents imparting durable antimicrobial properties to fabrics.

scholarly journals In Situ Gel Formation in Microporated Skin for Enhanced Topical Delivery of Niacinamide

Pharmaceutics ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 472 ◽  
Author(s):  
Sonalika Bhattaccharjee ◽  
Moritz Beck-Broichsitter ◽  
Ajay K. Banga
Keyword(s):  
Molecular Weight ◽  
Sol Gel ◽  
Topical Delivery ◽  
Needle Length ◽  
Molecular Weight Polymer ◽  
Sol Gel Transition ◽  
Pre Treatment ◽  
Franz Diffusion Cells

Although used widely in cosmetic formulations, topical delivery of niacinamide (LogP = −0.35) is unfavorable by conventional means. Poly(lactide-co-glycolide) (PLGA) formulations, can undergo a sol-gel transition triggered by solvent exchange, entrapping molecules and sustaining their release. The current study aims to exploit the ability of PLGA to gel in situ and enhance the topical delivery of niacinamide in microporated skin. In vitro drug permeation studies were performed using vertical Franz diffusion cells. Microporation was performed using Dr. PenTM Ultima A6, where pre-treatment with a 1 mm needle-length for 10 s and a 0.5 mm needle-length for 5 s, both at 13,000 insertions/min were compared. The effect of different grades of PLGA, EXPANSORB® DLG 50-2A (“low” molecular weight), and EXPANSORB® DLG 50-8A (“high” molecular weight) on topical delivery was also determined. Formulations containing PLGA resulted in successful gelation in situ on application over microporated skin. A significantly higher amount of drug was found in the skin with the 0.5 mm treatment for 5 s (892 ± 36 µg/cm2) than with 1 mm for 10 s (167 ± 16 µg/cm2). Hence, the different grades of PLGA were evaluated with 0.5 mm, 5 s treatment, and a significantly larger amount was seen in skin with the higher rather than the lower molecular weight polymer (172 ± 53 µg/cm2).

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