Co-reporter:Qiufeng An;Jiayan Pan;Bei Zhang;Tingting Wang
Fibers and Polymers 2016 Volume 17( Issue 7) pp:1069-1077
Publication Date(Web):2016 July
DOI:10.1007/s12221-016-6296-z
A novel dodecylphenylsiloxane oligomer resin/nanocomposite (PHDESR-SiO2) was prepared by graft copolymerization between dodecyl modified phenylsiloxane resin with pendent epoxy groups (PHDESR) and amino-functionalized silica nanoparticles (BTEPA-SiO2). PHDESR-SiO2 was then used to prepare a super hydrophobic surface on cotton fabric by a facile solution-immersion process method. Chemical structures, chemical compositions, wettability, surface morphology, and thermal properties were investigated by Fourier Transform Infrared Spectrum (FT-IR), 1H-NMR spectrum, X-ray photoelectron spectroscopy (XPS), static contact angle analyzer, scanning electron microscopy (SEM), Particle size distribution (PSD) and thermo-gravimetric analysis (TGA). The results showed that the target product PHDESR-SiO2 has an anticipative structure with many micro/nanostructure tubercles, a cross-linked network hydrophobic organosilicon resin film and many clusters of cylindrical dodecyl molecular brushes. This created super hydrophobic structure on the surface of the treated cotton fabrics. XPS analysis indicated that the long carbon chain groups had a slight tendency to enrich the film-air interface. In addition, PHDESR-SiO2 can provide good hydrophobicity for the treated fabric. As the dose of PHDESR-SiO2 increased, the hydrophobicity of the treated fabric enhanced and consequently the water static contact angle reached 152.5 °. This had little influence on the softness, color, and gas permeability of the fabrics. This makes it slightly stiff at high doses, and the super-hydrophobic cotton fabric also had good launderability.
Co-reporter:Qiufeng An;Jie Zhao;Xianqi Li;Yuanbo Wei;Wen Qin
Journal of Applied Polymer Science 2014 Volume 131( Issue 16) pp:
Publication Date(Web):
DOI:10.1002/app.40612
ABSTRACT
A novel comb-like polysiloxane (QPEPS) bearing dimethyldodecyl quaternary ammonium polyether groups (QPEs) was synthesized by reaction of epoxy polyether polysiloxane, which was prepared from polymethylhydrosiloxane (PHMS) and allyl polyether epoxy (APEE500) via hydrosilylation, with N,N-dimethyldodecylamine (DMDA) in the presence of acetic acid (HAc). Chemical structure, film morphology, and performance of the synthesized polysiloxane on cotton and its mimic substrates were investigated by Fourier transform infrared spectrum, nuclear magnetic resonance spectrum, field emission scanning electron microscopy, atomic force microscopy, and so on. As expected, the QPEPS was easily emulsified into a clear, uniform micro-emulsion with a mean size of about 20 nm. Since the presence of a large number of cationic QPEs pendant in the side chains, the QPEPS exhibited microscopic inhomogeneous morphology with many pinnacles projected on the film surface. As a result, the root mean square roughness (Rq) of the QPEPS film reached 0.615 nm in 2 µm × 2 µm scanning field and the largest height of the pinnacles achieved 7.618 nm. And under the influence of the QPEs, the QPEPS provided the treated fabrics with not only very soft handle, but also excellent hygroscopicity. And the wettability of the treated fabrics reached 1–3 s. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40612.
Co-reporter:Jie Zhao;Xianqi Li;Wei Xu
Fibers and Polymers 2014 Volume 15( Issue 10) pp:2112-2117
Publication Date(Web):2014 October
DOI:10.1007/s12221-014-2112-9
The supramolecule CPES/ASO was self-assembled from carboxylated polyether-block-polydimethylsiloxane (CPES) and N-β-aminoethyl-γ-aminopropyl polysiloxane (ASO) in ethyl acetate solution. The film morphology and performance of CPES/ASO on cotton substrates were investigated by field emission scanning electron microscope (FESEM), atomic force microscope (AFM), X-ray photoelectron microscope (XPS), and so on. The results indicated that a polysiloxane resin film was coated on the treated fiber surface and able to decrease the root mean square roughness (Rq) of the treated fiber conspicuously. Morphology of higher peaks circled by many smaller peaks was observed on the film surface, which was partly similar to that of CPES/ASO on the silicon wafer. Besides, when the mass ratio of CPES to ASO was 2:1, the fabric treated by CPES/ASO showed the best softness and had a comfortable oily tactile.
Co-reporter:Qiufeng An;Wei Xu;Lifen Hao;Yongshan Fu ;Liangxian Huang
Journal of Applied Polymer Science 2013 Volume 128( Issue 5) pp:3050-3056
Publication Date(Web):
DOI:10.1002/app.38503
Abstract
Superhydrophobic coating was developed on cotton fabric in this article using a dodecafluoroheptyl-containing polyacrylate (DFPA) and nanosilica. Film morphology of DFPA on cotton fibers/fabrics and chemical compositions of the treated cotton fabric were investigated using scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS), respectively. DFPA could form a relatively even film on the cotton fabric/fiber under SEM observation; however, it presented a rough and microphase-separated pattern under AFM observation. There were many mountain-like protuberances. The height of the protuberances and the root mean square roughness (Rms) of the film reached about 20–50 nm and 12.511 nm in 2 × 2-μm2 scanning field (as the scale data was 100 nm). XPS analysis indicated that the perfluoroalkyl groups had the tendency to enrich at the film–air interface. DFPA could make the treated cotton fabric with a water contact angle (WCA) at about 138.5°. Cotton fabric was previously roughened using a 1 wt % silica sol with an average particle size of 20–30 nm and then finished by DFPA; hydrophobicity of the resultant cotton fabric was strongly improved, and WCA could reach 153.6°. The color of this superhydrophobic fabric would not be influenced, but its softness decreased compared to untreated fabric. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013
Co-reporter:Wei Xu;Lifen Hao;Zhe Sun;Wenjing Zhao
Journal of Polymer Research 2013 Volume 20( Issue 2) pp:
Publication Date(Web):2013 February
DOI:10.1007/s10965-012-0069-1
Cationic fluorinated polyacrylate soap-free latexes (CFMBD) with core-shell structure were prepared by co-polymerizing dodecafluoroheptyl methacrylate (DFMA), methyl methacrylate (MMA), butyl acrylate (BA), and dimethylaminoethyl methacrylate (DM) using a novel cationic polymerisable emulsifier, maleic acid double ester-octadecyl poly(ethyleneoxy)20 ether-ethylene trimethyl ammonium chloride (R303). FT-IR spectra and 1H-NMR spectra confirmed that DFMA successfully participated in emulsion polymerization. The resulted emulsion particles had a core-shell structure. Compared with the latex prepared by mixed 1831/AEO-9 emulsifiers, the latexes prepared by R303 emulsifier had higher surface tension. In addition, hydrophobicity of the CFMBD latex film was superior to that of the general latex film under the same conditions. Those latex films showed the increasing thermal stability with augment of DFMA amount in polymer compared to fluorine-free one. XPS analysis indicated the fluoroalkyl groups had the tendency to enrich at the film-air interface. The fluorine-free latex film showed the relatively smooth surface morphology in its AFM image, however, there were numerous little protuberances on the film surface of the CFMBD latex from the polymer containing 27.5 wt% DFMA in total monomers weight dried at room temperature. Especially, after the annealing process, some peaks and lots of protuberances on that film appeared and the surface roughness was greatly increased. Water contact angles (WCAs) of fluorine-free latex film, that CFMBD film dried at room temperature and after the annealing process could attain 62.5°, 102.5° and 108.5°, respectively.
Co-reporter:Qiufeng An;Qianjin Wang;Yan Wang;Liangxian Huang
Fibers and Polymers 2009 Volume 10( Issue 1) pp:40-45
Publication Date(Web):2009 February
DOI:10.1007/s12221-009-0040-x
A water-soluble polysiloxane (PE-PUVSi) bearing functional benzophenone derivative and hydrophilic polyether side groups was successfully synthesized by hydrosilylation of polyhydromethylsiloxane (PHMS) with 2-hydroxy-4-(β-allyloxy-γ-hydroxy)propyloxy benzophenone (MUV-O) and allyl polyoxyethylenepolyoxypropylene ether (F6). The chemical structure, film morphology, and performance of the synthesized polysiloxane were investigated and characterized by spectral analysis, atomic force microscope (AFM), Kawabata evaluation system (KES), and other instruments. Experiment results indicate that PE-PUVSi had an intensive UV-absorbing capacity at wavelengths of 243.6, 289.2, and 325.0 nm. It formed a hydrophilic polysiloxane film on both the fiber and the silicon wafer surface. On the wafer surface, PE-PUVSi actually showed non-homogeneous and phase-separated microscopic film morphology. In addition, PE-PUVSi could provide a bulky softness, good wettability, and antistatic property for the treated fabric and make the treated cotton fabric show a low UV transmittance at the wavelengths between 270 and 330 nm.
Co-reporter:Qiufeng An;Gang Yang;Qianjin Wang ;Liangxian Huang
Journal of Applied Polymer Science 2008 Volume 110( Issue 5) pp:2595-2600
Publication Date(Web):
DOI:10.1002/app.28749
Abstract
In this research, hydroxyl-terminated polyether-block-polydimethylsiloxane (PESO) was synthesized as an intermediate through the hydrosilylation of SiH-terminated polydimethylsiloxane with allyl polyoxyethylene polyoxypropylene ether. Then, carboxylated polyether-block-polydimethylsiloxane (CPES) was prepared through the reaction of maleic anhydride with PESO. First, the chemical structures of the synthesized polysiloxanes were characterized with IR and 1H-NMR spectroscopy, and then the film morphology of CPES and the supermolecule self-assembled from CPES and N-β-aminoethyl-γ-aminopropyl polydimethylsiloxane (ASO-1) was investigated by atomic force microscopy in detail. Experimental results indicated that the superpolysiloxane that self-assembled from CPES and ASO-1 showed a film morphology very different from those of CPES and ASO-1. There were not only many small, bright dots but also some big and marvelous dots circled by dots on the film surface. The morphology of dots circled by dots was estimated to result from aggregates of CPES micelles adsorbed onto the curled ASO-1 molecule interface. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008
Co-reporter:Qiufeng An;Linsheng Li;Dedai Lu;Liangxian Huang
Journal of Applied Polymer Science 2007 Volume 104(Issue 1) pp:
Publication Date(Web):25 JAN 2007
DOI:10.1002/app.25739
A novel functional polysiloxane (PSBP) bearing benzophenone derivatives as UV absorbing side groups was synthesized by hydrosilylation of polyhydromethylsiloxane (PHMS) with 2-hydroxy-4-(β-hydroxy-γ-allyloxy)propyloxy benzophenone (HHAPB). The chemical structure, film morphology, and the softening fabric property of the synthesized polysiloxane were characterized and investigated by spectrum analysis, atomic force microscope (AFM), and Kawabata evaluation system. The experiment results indicated that PSBP was not only an excellent polymeric UV-absorber, which showed intensive ultraviolet absorptions respectively, at wavelengths of 243.2, 288.2, and 325.4 nm, but could exhibit a nonhomogeneous, some rough structure film on silicon wafer substrate. In addition, the functional side group, benzophenone derivative as well as its mass ratio to PSBP has an influence on the performance of the synthesized polysiloxane. As the mass ratio decreased from 31.48 to 12.87%, the molar extinction coefficients εmax (λmax = 288.2 nm) of the PSBP fluids lowered from 3.4564 × 105 to 1.5763 × 105, but while the softening fabric properties of PSBP on cotton fabrics increased. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 680–687, 2007
Co-reporter:Qiufeng An;Guangwen Cheng;Linsheng Li
Journal of Applied Polymer Science 2006 Volume 101(Issue 6) pp:4480-4486
Publication Date(Web):27 JUN 2006
DOI:10.1002/app.24288
A novel polysiloxane softener bearing dodecyl side groups (dodecylpolysiloxane [DDPS]) was synthesized by copolymerization of octamethylcyclotetrasiloxane with dodecyltrimethoxysilane and hexamethyldisiloxane. Chemical structure and film morphology of the synthesized polysiloxane are characterized and investigated by infrared spectrum, 1H-NMR, field emission scanning electronic microscope, and atomic force microscope. The experiment results indicate that DDPS can form a hydrophobic film on both the cotton fiber and silicon wafer surface. At an amplification of <80,000 (of the original fiber) and the observation rule (working distance) of >200 nm, DDPS shows a relative smooth resin film on the treated fabric/fiber surface. But as the observation rule decreases to 2 nm—almost to a molecular scale—the DDPS film mostly exhibits an inhomogeneous structure and uneven morphology in its atomic force microscope images. There are many low or high peaks that appeared in DDPS topography. Consequently in 2 μm2 scanning field, the root mean square roughness of DDPS film reaches to 0.199 nm, which is 2.46 times rougher as compared with that of polydimethylsiloxane film. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 4480–4486, 2006