Synthesis of acrylic acid grafted silicone rubber via preirradiation graft copolymerization and its physical and dielectric properties

The hydrophilic monomer, acrylic acid (AA), has been grafted onto hydrophobic silicone rubber (SR) film via the γ-ray preirradiation graft technique. The AA percent graft in SR-g-AA film increases with increasing irradiation dose rate. The iron powder in monomer solution serves as one source of ferrous ion that is generated by the oxidation reaction with water. The swelling effect shows that the amount of chloroform taken up by an SR-g-AA membrane decreases with the increasing AA grafting, and the amount of water, alcohol, and glycerol taken up by an SR-g-AA film increases with increasing AA percent grafting. The contact angle, ultimate stress, and elongation at break of SR and SR-g-AA copolymers decrease with increasing AA percent grafting. The oxygen/nitrogen selectivity in these films can be enhanced by the graft modification. The thermal behaviors of SR-g-AA copolymers show the characteristics of SR and polyacrylic acid. Finally, the dielectric properties show that the SR-g-AA film has a superior dielectric property than the original SR and poly(AA) matrix. © 1996 John Wiley & Sons, Inc.     

Dialysis membranes from polyethylene films grafted with acrylic acid

Low‐density polyethylene‐g‐poly(acrylic acid) membranes were prepared by the direct radiation grafting of aqueous acrylic acid solutions (containing Mohr's salt) onto low‐density polyethylene films and were irradiated at two different irradiation doses (2 and 3 Mrad) at a dose rate of 0.02 Mrad/h. Two series of polyethylene‐g‐poly(acrylic acid) membranes with 100 and 150% grafting were obtained. The free carboxylic acid groups in the grafted films were converted into the corresponding acrylates by reactions with different metal salts. The swelling (water uptake) and dialysis permeability of glucose and urea through the grafted membranes in different metal‐ion forms were investigated. The prepared membranes showed good permeability to both solutes, which increased as the hydrophilicity of the membrane increased. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 10–14, 2004     

Simple and feasible strategy to fabricate microcellular poly(butylene succinate) foams by chain extension and isothermal crystallization induction

In this article, a facile and efficient isothermal crystallization induction method was proposed to fabricate microcellular poly(butylene succinate) (PBS) foams with supercritical CO₂. The good regularity of PE chain segments and high reactive epoxy groups in ethylene-glycidyl methacrylate copolymer (PE-g-GMA) serving as a chain extender were employed to improve the crystallization behaviors, viscoelasticity, and foaming behaviors of PBS through chain extension reaction. The effect of PE-g-GMA content on the thermal properties, rheological performances, and cellular morphology of various PBS samples was investigated systematically. When the PE-g-GMA content switched from 7.5 to 10 wt %, an interesting transition from fine cells to microcells was observed in PBS/PE-g-GMA foams. Microcellular PBS foam modified by 10 wt % PE-g-GMA was successfully prepared at the foaming temperature of 87 °C and the induction time of 7 min, in which its cell size and cell density could reach 6.63 ± 1.93 μm and 3.75 × 10⁹ cells cm⁻³, respectively. The formation of abundant but tiny spherocrystals in chain extended PBS samples made a considerable contribution for preparing microcellular PBS foams. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48850.     

Si@S-doped C anode with high cycling stability using PVA-g-PAA water soluble binder for lithium-ion batteries

The nanostructured Si@S-doped C (Si/C) hybrid is synthesized via a mild hydrothermal process of glucose and the simultaneous polymerization of 3,4-ethylenedioxythiophene and poly(sodium-4-styrene sulfonate) on the surface of nano-Si powders, then followed by a calcination process. A new water soluble polymer of poly(vinyl alcohol) (PVA) grafted with poly(acrylic acid) (PAA) is synthesized via a free-radical polymerization of acrylic acid (AA) in a 1:1 weight ratio in PVA water solution. The Si/C anode using PVA-g-PAA binder, exhibits improved lithium storage properties and cycling stability than that of the parallel electrode with carboxymethyl cellulose binder, which exhibits an initial coulombic efficiency (82.0%), even a reversible capacity of 487 mAh g⁻¹ after 300 cycles with 81.2% capacity retention at 0.4 A g⁻¹. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48764.     

A comparison of the structure, thermal properties, and biodegradability of polycaprolactone/chitosan and acrylic acid grafted polycaprolactone/chitosan

The effects of replacing PCL with acrylic acid grafted PCL (PCL-g-AA) on the structure and properties of a PCL/chitosan composite were investigated. The properties of both PCL-g-AA/chitosan and PCL/chitosan were examined and compared using FTIR, ¹H and ¹³C nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), and a biodegradation test. With PCL-g-AA in the composite, compatibility with chitosan and, consequently, the properties of the blend were both much improved due to the formation of ester and imide groups that conferred better dispersion and homogeneity of chitosan in the matrix. Moreover, PCL-g-AA/chitosan had a lower melt temperature and was, therefore, more easily processed than PCL/chitosan. Resistance to water was higher in the PCL-g-AA/chitosan blend, and consequently so was its resistance to biodegradation in soil and in an enzymatic environment. Nevertheless, weight loss of blends buried in soil or exposed to an enzymatic environment indicates that both blends were biodegradable, especially at high levels of chitosan content. Both blends suffered deterioration in tensile strength and elongation at break after exposure to soil or enzymatic environments.     

Melt Functionalization of Ethylene-Propylene Copolymer: Structural Investigation

An ethylene-propylene copolymer (EPM) has been functionalized with acrylic acid (AA) by means of a radical-initiated melt process. Different degrees of grafting have been obtained by varying the overall composition of the reaction mixture. The influence of the grafting degree on the structure has been investigated by differential scanning calorimetry (DSC), Fourier-transform infrared analysis (FTIR), and wide-angle x-ray scattering (WAXS) techniques. The results of the structural investigations suggest that the grafting preferentially occurs onto the ethylene sequences of EPM. After acrylic acid was grafted onto EPM, the grafted AA acted as nucleation agent; it caused an increase of crystallization temperature of propylene sequences of EPM-g-AA.     

Effect of Polyethylene-Grafted Maleic Anhydride (PE-g-MAH) on Properties of Low Density Polyethylene/Eggshell Powder (LDPE/ESP) Composites

The effect of polyethylene-grafted maleic anhydride (PE-g-MAH) on the tensile properties, morphology and thermal properties of low-density polyethylene (LDPE)/eggshell powder (ESP) composites was studied. LDPE/ESP composites with different eggshell powder content and the addition of PE-g-MAH were prepared with Z-blade mixer at 180°C and rotor speed of 50 rpm. The tensile strength, elongation at break and thermal stability of LDPE/ESP composites with PE-g-MAH were greater than LDPE/ESP composites, and their differences became more pronounced at higher filler content. The interfacial adhesion between ESP and LDPE was improved with the addition of PE-g-MAH as evidenced by the morphological study.     

Grafting reactions onto poly(organophosphazenes). IV. Light-induced graft copolymerization of organic polymers containing free acid or basic functionalities onto poly[bis(4-benzylphenoxy)phosphazene]

The light-induced graft copolymerization of acrylic acid, methacrylic acid, and 4-vinylpyridine onto poly[bis(4-benzylphenoxy)phosphazene] films to prepare new grafted phosphazene copolymers containing acid and basic functionalities is reported. The process was carried out in monomer/methanol mixtures in the presence of benzophenone or benzoin ethyl ether as photosensitizers by selective excitation of these last species. The yield of the grafting processes was evaluated as a function of the monomer concentration in the reaction medium, type of photoinitiator, and characteristics of the grafted organic monomers. The acid functions inserted in poly[bis(4-benzylphenoxy)phosphazene]-g-poly(meth)acrylic acid grafted copolymers, and the basic groups of the poly[bis(4-benzylphenoxy)phosphazene]-g-poly-4-vinylpyridine substrates were allowed to interact with basic and acid dyes, respectively, to form permanently colored polymeric films. The photoactivity of these films as substrates for the photosensitized production of singlet oxygen was tested. © 1995 John Wiley & Sons, Inc.     

Two-Dimensional Texture of Intrinsic Conductive Poly(styrene-co-maleanilic Acid) Grafted with Polyaniline: Formation and Conductivity

Intrinsically conducting polyaniline is grafted onto a preformed poly(styrene-co-maleanilic acid) copolymer backbone via chemical oxidative coupling of aniline in acidified chloroform/water emulsion. The structure and textural morphology of the grafted poly(S-co-MA-g-PANI) are examined by different spectroscopic, thermal, powder X-ray diffraction and scanning electron microscopic techniques. The d.c. electrical conductivity of the grafted emeraldine base of the obtained materials displays a d.c. conductivity of the order of 10^?7 – 10^?9 Scm^?1, which is ～2 orders of magnitude greater than that of the reported PANI-EB homopolymer. This enhancement in d.c. conductivity is explained in terms of microstructure-electronic conductivity relationship.     

Graft copolymerization of acrylic acid to nylon 6 by mutual irradiation. II. The influence of cupric ions

In the γ-irradiation in vacuo of nylon 6 film in the presence of aqueous acrylic acid and different concentrations of cupric chloride, the following relationships have been obtained: R_H ∝ [CuCl₂]^?1.0 and R_G ∝ [CuCl₂]^?0.3 Here [CuCl₂] is the concentration of cupric chloride in the bulk solution, and R_H and R_G denote the initial rates of homopolymerization and grafting, respectively. The values of ?1.0 and ?0.3 for the exponents indicate that the cupric ion is a less effective chain terminator in the film on account of its lower concentration there. Analyses of films grafted in different media demonstrate the copper content of a film to be independent of both the concentration of monomer in the solution and the degree of swelling. The copper content is primarily a function of the total poly(acrylic acid) present, i.e., (grafted species plus occluded homopolymer). Thus, at high doses, where the total poly(acrylic acid) associated with a film is significant, the grafting curves exhibit a falling off, and complex formation between cupric ion and a growing chain is considered a likely contributory factor.     

Control of biodegradability of poly(3‐hydroxybutyric acid) film with grafting acrylic acid and thermal remolding

Radiation‐induced graft polymerization of acrylic acid (AAc) on poly(3‐hydroxybutyric acid) (PHB) film was carried out and the resulting film was thermally‐remolded. The PHB films grafted with AAc (PHB‐g‐AAc) having a degree of grafting higher than 5% completely lost the enzymatic degradability. The enzymatic degradability of the grafted film was recovered by thermal remolding. The highest enzymatic degradation rate was observed at degree of grafting of 10% after thermal remolding. The PHB‐g‐AAc films and thermally‐remolded PHB‐g‐AAc films were characterized by contact angle and differential scanning calorimetry. The enzymatic degradability of PHB‐g‐AAc films was lost by the grafted AAc, which covered the surface of PHB film. The acceleration of enzymatic degradation in the remolded PHB‐g‐AAc films was mainly caused by decrease of crystallinity of PHB by dispread of grafted AAc during thermal remolding. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3856–3861, 2006     

Physicochemical investigation of radiation‐grafted poly(acrylic acid)‐graft‐poly(tetrafluoroethylene–ethylene) copolymer membranes and their use in metal recovery from aqueous solution

ET‐g‐PAAc membranes were obtained by radiation grafting of acrylic acid onto poly(tetrafluoroethylene–ethylene) copolymer films using a mutual technique. The ion selectivity of the grafted membranes was determined toward K⁺, Ag⁺, Hg²⁺, Co²⁺, and Cu²⁺ in a mixed aqueous solution. The ion‐exchange capacity of the grafted membranes was measured by back titration and atomic absorption spectroscopy. The Hg²⁺ ion content of the membrane was more than that of either the K⁺ or Ag⁺ ions. The presence of metal ions in the membranes was studied by infrared and energy‐dispersive spectroscopy measurements. Scanning electron microscopy of the grafted and metal‐treated grafted membranes showed modification of the morphology of the surface due to the adsorption of K⁺ and Ag⁺ ions. No change was observed for the surface of the membrane that was treated with Hg²⁺ ions. The thermal stability of different membranes was improved more with Ag⁺ and Hg²⁺ ions than with K⁺ ions. It was found that the modified grafted membranes possessed good hydrophilicity, which may make them promising candidates for practical applications, such as for cation‐exchange membranes in the recovery of metals from an aqueous solution. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2692–2698, 2002     

Design and electrical conductivity of poly(acrylic acid‐g‐gelatin)/graphite conducting gel

A novel poly(acrylic acid‐g‐gelatin)/graphite composite is synthesized by aqueous solution polymerization. Based on the electrical conductivity of graphite nanoplatelets and the absorbency of poly(acrylic acid‐g‐gelatin)/graphite, a novel conducting gel with a conductivity of 3.18 mS cm^?1 is prepared. The effects of synthesis parameters on the electrical conductivity of the gels are investigated in detail. An appended network structure model of the poly(acrylic acid‐g‐gelatin)/graphite conducting gel is proposed. The conducting gel presents a high mechanical strength in cyclohexane, which is important for the gel applications. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers     

Polypropylene/polypropylene‐grafted acrylic acid blends for multilayer films: Preparation and characterization

Polypropylene (PP) was functionalized with acrylic acid (AA) and styrene (st) as a comonomer by means of a radical‐initiated melt‐grafting reaction. FTIR, ESCA, and ¹H‐NMR spectroscopies were used to characterize the formation of polypropylene grafted with acrylic acid (PP‐g‐AA) and polypropylene grafted with acrylic acid and styrene (PP‐g‐AAst). The content of AA grafted onto PP was determined by using volumetric titration. Blends of PP with 0–100 wt % of PP‐g‐AA were prepared by melt mixing. The effect of the modified polymer content on the surfaces of cast films was characterized through FTIR–ATR and ESCA analysis as well as contact‐angle, wetting‐tension, and ink‐adhesion measurements. The influence of the content of AA on the melting and crystallization temperature of PP was investigated by DSC. The contact angles of water on cast‐film surfaces of PP/PP‐g‐AA blends decreases with increasing modified polymer content and decreasing PP‐g‐AA molecular weight. A notorious improvement on wetting tension was observed with increasing modified polymer content and decreasing PP‐g‐AA molecular weight. From FTIR–ATR and ESCA spectra of the blends, a calculation was made of the carbonyl index on the films' surfaces. It was found that the higher the carbonyl index, the lower the contact‐angle value for the polypropylene blends. An increase in crystallization temperature of PP was observed when AA monomers were grafted into PP and with increasing PP‐g‐AA content in the blend, probably caused by a nucleation effect of AA monomers that would improve the crystallization capability of PP. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1497–1505, 2001     

Synthesis and characterization of cassava starch graft poly(acrylic acid) and poly[(acrylic acid)‐co‐acrylamide] and polymer flocculants for wastewater treatment

Starch‐g‐poly(acrylic acid) and poly[(acrylic acid)‐co‐acrylamide] synthesized via chemically crosslinking polymerization were then each mixed with inorganic coagulants of aluminum sulfate hydrate [Al₂(SO₄)₃·18H₂O], calcium hydroxide [Ca(OH)₂], and ferric sulfate [Fe₂(SO₄)₃] in a proper ratio to form complex polymeric flocculants (CPFs). All CPFs exhibited low water absorbency than those of the uncomplexed superabsorbent copolymers. The color reduction by the CPFs was tested with both synthetic wastewater and selected wastewater samples from textile industries. The synthetic wastewater was prepared from a direct dye in a concentration of 50 mg dm^?3 at pH 7. The CPFs of poly[(acrylic acid)‐co‐acrylamide] with calcium hydroxide at a ratio of 1:2 is the most effective CPF for the wastewater color reduction. The CPF concentration of 500 mg dm^?3 could reduce the color of the synthetic wastewater containing the direct dye solution by 95.4% and that of the industrial wastewater by 76%. Starch‐g‐poly(acrylic acid)/Ca(OH)₂ CPF can reduce the synthetic direct dye and the industrial wastewater by 74% and 18%, respectively. Chemical oxygen demand, residual metal ion concentrations, pHs, turbidity of the wastewater were also investigated and the potential use of the complex polymer flocculants for textile wastewater treatment was indicated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2915–2928, 2006     

Syntheses,characterization, and antibacterial activity of chitosan grafted hydrogels and associated mica‐containing nanocomposite hydrogels

Chitosan (CS) grafted poly[(acrylic acid)‐co‐(2‐hydroxyethyl methacrylate)] (CS‐g‐poly(AA‐co‐HEMA)) at different molar ratios of AA and HEMA, and the associated nanocomposite hydrogels of CS‐g‐poly(AA‐co‐HEMA)/mica were synthesized by radical copolymerization. The grafting positions at the amino or hydroxyl groups in the CS were identified by Fourier transform infrared spectroscopy. CS‐g‐poly(AA‐co‐HEMA) hydrogels were intercalated in the mica and the amount of hydrogel insertion did not affect the spacing of the silicate layers in mica. The higher mica loadings produced a rougher surface of the nanocomposite hydrogel. The water absorbency of the CS‐g‐poly(AA‐co‐HEMA)/mica nanocomposite hydrogels decreased with increasing levels of mica loading to a lower level than those of the CS‐g‐poly(AA‐co‐HEMA) hydrogels. Both CS‐g‐poly(AA) and CS‐g‐poly(AA‐co‐HEMA)/mica nanocomposite hydrogels exhibited a higher antiproliferative activity against Staphylococcus aureus than did the neat CS hydrogel with CS‐g‐poly(AA) revealing a very pronounced minimum inhibition concentration (MIC) of 1.56 mg mL^?1. The extent of mica loading in the CS‐g‐poly(AA‐co‐HEMA) nanocomposite hydrogels did not affect the MIC (12.5 mg mL^?1). © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis and characterization of a poly(acrylic acid)‐graft‐methoxy poly(ethylene oxide) comblike copolymer

A methoxy poly(ethylene oxide) (MPEO) grafted poly(acrylic acid) (PAA) comblike copolymer was synthesized by the direct condensation of MPEO onto the PAA backbone in the presence of dicyclohexyl dimethylcarbodiimide (DCC) and 4‐dimethylaminopyridine (DMAP). Its chemical structure was characterized by Fourier transform infrared and ¹H‐NMR spectroscopies. The effects of different catalysts, solvents, reaction temperatures, and reaction times on the grafting degree of the PAA‐g‐MPEO comblike copolymer were investigated. Compared to p‐toluene sulfonic acid, DMAP/DCC as a catalyst markedly increased the grafting degree. The optimum reaction conditions were a tetrahydrofuran/water mixture solvent, a reaction temperature of 50°C, and a reaction time of 168 h. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Preparation of biocompatible multi‐walled carbon nanotubes as potential tracers for sentinel lymph nodes

Carbon nanotubes (CNTs) are capable of traversing cellular membranes by endocytosis and are therefore promising materials for use in imaging and drug delivery. Unfortunately, pristine CNTs are practically insoluble and tend to accumulate inside cells, organs and tissues. To overcome the poor dispersibility and toxicity of pristine CNTs, hydrophilic functionalization of CNTs has been intensively investigated. Water‐soluble multi‐walled carbon nanotubes (MWCNTs) were prepared by in situ polymerization of acrylic acid in a poor solvent for poly(acrylic acid) (PAA). The solvent type influenced the grafted density and chain length of PAA. MWCNTs with a high grafted density of PAA (22 wt%) could be well dispersed in water, NaCl aqueous solution (0.9 wt%) and cell culture media. The in vitro cytotoxicity of these MWCNTs for endothelial cells is reasonably low even at high concentration of PAA‐g‐MWCNT (70 µg mL^?1). The experimental results show that the biocompatibility of these MWCNTs is sufficient for biological applications. PAA‐g‐MWCNTs were successfully utilized for lymph node tracing. Experimental results suggest that PAA‐g‐MWCNTs have potential to be used as a vital staining dye, which may simplify the identification of lymph nodes during surgery. Copyright © 2009 Society of Chemical Industry     

The adsorption of Cu(II) ion from aqueous solution upon acrylic acid grafted poly(ethylene terephthalate) fibers

This study is concerned with the investigation of the adsorption properties of acrylic acid grafted poly(ethylene terephthalate) fibers by the use of Cu(II) ions in aqueous solutions. Influence of pH, graft yield, contact time, concentration of the ion, and reaction temperature on the amount of ion adsorbed upon reactive fiber were investigated. The time in which the adsorption reached to the equilibrium value was determined as 1 h. The adsorption isotherm of Cu(II) ion was found to be a Langmuir type and the heat of adsorption was calculated as ?10.1 kJ mol^?1. It was observed that the adsorbed Cu(II) ion upon acrylic acid grafted poly(ethylene terephthalate) fibers could be recovered in acidic media. The fiber could also readsorb Cu(II) ions without losing its activity. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1216–1220, 2003     

The study of surface segregation and the formation of gradient domain structure at the blend of poly(methyl methacrylate)/poly(dimethyl siloxane) graft copolymers and acrylate adhesive copolymers

The effect of siloxane chain length on surface segregation of poly(methyl methacrylate)‐grafted poly(dimethyl siloxane) (PMMA‐g‐PDMS)/poly(2‐ethylhexyl acrylate‐co‐acrylic acid‐co‐vinyl acetate) [P(2EHA‐AA‐VAc)] blends was investigated. The blends of PMMA‐g‐PDMS with P(2EHA‐AA‐VAc) showed surface segregations of PDMS components. The surface enrichments of PDMS in the blends depended significantly on the PDMS chain length. Also, this blend showed the gradient domain structure. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 375–380, 2003