Fabrication of reverse‐osmosis membranes for the desalination of underground water via the γ‐radiation grafting of acrylic acid onto polyethylene films
Abstract:Research has been devoted to the desalination of saline water to fresh water suitable for human demands because of the shortage of water in some countries. Therefore, in this study, reverse-osmosis membranes were prepared via the g-radiation graft copolymerization of acrylic acid onto high-density and low-density polyethylene. The factors that could affect the grafting process, such as the solvent type, monomer and inhibitor concentration, and irradiation dose, were investigated to determine the optimum condit… Show more
“…Radiation technique is often used for radiation modification of polymer materials because of its simple experimental conditions, mild reaction and easy control. 27 Considering the non-selective nature of gamma-ray interactions, 27 radiation grafting techniques allow the grafting of vinyl monomers onto a variety of polymer substrates without the need for initiators and specific functional groups. 28 Cotton fiber material is one of the matrix materials commonly used for radiation modification.…”
Silver nanocluster composites are obtained directly through radiation technology and can be used to catalyse 4-nitrophenol reduction and sodium borohydride. The catalyst is a candidate for the treatment of water contaminant 4-NP and the production of hydrogen from NaBH4.
“…Radiation technique is often used for radiation modification of polymer materials because of its simple experimental conditions, mild reaction and easy control. 27 Considering the non-selective nature of gamma-ray interactions, 27 radiation grafting techniques allow the grafting of vinyl monomers onto a variety of polymer substrates without the need for initiators and specific functional groups. 28 Cotton fiber material is one of the matrix materials commonly used for radiation modification.…”
Silver nanocluster composites are obtained directly through radiation technology and can be used to catalyse 4-nitrophenol reduction and sodium borohydride. The catalyst is a candidate for the treatment of water contaminant 4-NP and the production of hydrogen from NaBH4.
“…[12][13][14][15] The grafting process can be achieved using different strategies, including free-radical initiators, ionizing radiation (electron beam, γ-ray, and X-ray) and, UV radiation. [16][17][18][19] The significant problems of these procedures are consist of: little control over the graft operations onto PE backbone, the wide dispensation of molecular weight, a long-lasting modification effect, difficulties in achieving uniform modification, chain depression of PE backbone during the organization of free radical polymerization places, as well as the attendance of it's as a significant of homopolymer in the production. [20][21][22] For many years, many scholars have the intention to apply reversible impoverished radical polymerization (RIRP) for the synthesis of HDPE-based nanocomposite with well-explanatory structures.…”
Section: Introductionmentioning
confidence: 99%
“…Another affections and versatile approach for surface modification of PE are the grafting of other polymers onto the PE backbone [12–15] . The grafting process can be achieved using different strategies, including free‐radical initiators, ionizing radiation (electron beam, γ‐ray, and X‐ray) and, UV radiation [16–19] . The significant problems of these procedures are consist of: little control over the graft operations onto PE backbone, the wide dispensation of molecular weight, a long‐lasting modification effect, difficulties in achieving uniform modification, chain depression of PE backbone during the organization of free radical polymerization places, as well as the attendance of it's as a significant of homopolymer in the production [20–22] .…”
A well-defined method for discovering an easy and effective strategy through graft copolymer derived from poly (methylmethacrylate) (PMMA) as a monomer, high-density polyethylene (HDPE) and its organoclay nanocomposite with physicochemical and mechanical properties was successfully prepared by reversible addition-fragmentation transfer (RAFT) polymerization, and factors organoclay (Cloisite® 20 A) on the terminal features of the obtained graft copolymer were investigated. First, maleic anhydride (MA) was grafted onto HDPE directed by, the inauguration of an anhydride chain with ethanolamine to develop a hydroxylated high-density polyethylene (HDPE-OH). After that, the hydroxyl masses were esterified by using RAFT agent, 4-cyano-4-[(phenyl carbon thionyl) sulfanyl valeric acid to obtain HDPE-CTA macroinitiator. Then, the MMA monomer was grafted onto HDPE via the RAFT method to obtain the HDPE-g-PMMA graft copolymer. In the end, HDPE-g-PMMA/clay nanocomposite by a solution intercalation method was synthesized. The structures of the, copolymer and nanocomposite were studied by Fourier transform infrared spectroscopy, X-ray diffraction, and Transmission electron microscopy (TEM) techniques. It explores for the synthesis of HDPE-g-PMMA/clay nanocomposites, disclosed a foliated structure. Based on the thermic behavior, synthesized HDPE-g-PMMA/clay nanocomposites can display the above thermic solidity with just some extent (5) of organoclay.
“…In addition, the graft copolymers of synthetic polymers such as (poly(chloroethyl vinyl ether)‐g‐polystyrene)comb‐b‐(poly(chloropyran ethoxy vinyl ether)‐g‐polyisoprene)comb, (meth)acrylate copolymer grafted with long fluorinated side chain, Nylon 6‐g‐poly(acrylic acid), polyethylene‐g‐poly(acrylic acid), polyaniline‐g‐(sulfonated polyurethane), poly(N‐vinylpyrrolidinone‐g‐styrene), etc. are also reported . Depending on the chemical structure of reagents, more hydrophobic or more hydrophilic type graft copolymers than initial polymeric materials can be prepared …”
Novel amphiphilic, more environmentally friendly starch graft copolymers obtained by applying the “grafting from” method are prepared. The graft copolymerization of various ratios of citronellyl acrylate monomer and potato starch at 80 °C in the presence of potassium persulfate (1 wt.%) as an initiator is performed. The maximum of the grafting percent (%G) is observed for potato starch to monomer ratio 1:1.25 where ca. 1.8 hydroxyl groups per glycoside unit are covalently bonded with hydrophobic polymer chains. The graft materials are characterized by the attenuated total reflectance‐Fourier transform infrared spectroscopy (ATR‐FTIR), cross‐polarization magic angle spinning (13C CP/MAS NMR), and scanning electron microscopy (SEM). The performed analyses affirm the structure of the graft materials and confirm the creation of non‐porous copolymers with brief, heterogeneous surface. The selected physico‐chemical properties of the obtained graft copolymers such as ability to gelation, moisture absorption, swelling in polar and non‐polar solvents, chemical resistance, thermal properties, and pyrolysis mechanism are evaluated and compared with the previously tested starch‐g‐poly(citronellyl methacrylate) copolymers.
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