Poly(methyl acrylate)/Na‐montmorillonite intercalated composites: Preparation and characterization

Poly(methyl acrylate)/Na‐montmorillonite intercalated composites were prepared by free‐radical polymerization using benzoyl peroxide as a radical initiator in an aqueous medium. XRD patterns confirmed that the increase in interlayer spacing of Na‐montmorillonite (Na‐MMT) from 1.21 to 1.64 nm supports the intercalation. Although the width of the intercalated, delaminated montmorillonite aggregates are less than 100 nm (as seen in transmission electron microscopy), the prepared samples are members of the intercalated composite group. The samples exhibited better thermal stability than the pure polymer. Nitrogen adsorption capacity decreased due to the hindering of molecule diffusion and shielding of the intercalated aggregates by the polymer matrix. The decrease in moisture and water uptake of the samples indicated that the hydrophilic nature of montmorillonite changed greatly due to the hydrophobicity with increasing polymer content. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of Imidazolium–p-Chloro-phenacylide on Properties of Semi-interpenetrating Polymer Network from Poly(zinc acrylate) and Poly(styrene-co-methylmethacrylate)

The effect of nitrogen ylide, namely imidazolium–p-chlorophenacylide (ICPY), on the properties of semi-interpenetrating polymer network (semi-IPNs) of poly(zinc acrylate) as component I and styrene-co-methylmethacrylate as component II, using divinyl benzene as crosslinking agent, has been studied and compared with those obtained with α-α′-azobisisobutyronitrile (AIBN). The semi-IPNs have been characterized by infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry and scanning electron microscopy. The crosslink density as well as thermal stability of the IPNs synthesized in the presence of ylide (ICYP) is less than that with AIBN. © of SCI.     

Effect of bentonite on the physical properties and drug‐release behavior of poly(AA‐co‐PEGMEA)/bentonite nanocomposite hydrogels for mucoadhesive

A series of nanocomposite hydrogels for mucoadhesive were prepared from acrylic acid, poly(ethylene glycol) methyl ether acrylate, and intercalated bentonite clay by photopolymerization. The microstructures were identified by X‐ray diffraction (XRD). Results showed that the swelling ratio for the present nanocomposite hydrogels decreased with an increase of bentonite, whereas the gel strength and Young's modulus of the present gels increased with an increase of bentonite. However, the adhesive force of the present gels did not decrease with an increase of bentonite. XRD results indicated that the exfoliation of bentonite was achieved in the xerogels and swollen gels. Finally, the drug‐release behaviors for these gels were also assessed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2934–2941, 2004     

年产120吨聚丙烯酸钠絮凝剂的工艺设计与投产

介绍了新开发的生产工艺过程及工艺条件,对120吨/年的工厂设备选型、工厂经济分析及其应用效果作了简要评述。     

Synthesis and characterization of poly(glycidyl methacrylate)/Na‐montmorillonite nanocomposites

Poly(glycidyl methacrylate)/Na–montmorillonite nanocomposites were synthesized by free‐radical polymerization of glycidyl methacrylate containing dispersed montmorillonite. By changing the concentration of glycidyl methacrylate several polymer–clay nanocomposites were prepared and the resulting nanocomposites were characterized by X‐ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis. The results indicated that the properties of the composite were significantly improved. The thermogravimetric analysis results revealed that the degradation temperatures of nanocomposites were higher than that of pure polymer and the thermal degradation rates decreased. Examination of these materials by scanning electron microscopy showed that the clay layers are dispersed homogenously in the polymer matrix and the formation of intercalation nanostructure. Furthermore, adsorptive, moisture regain, and water uptake properties of nanocomposites were also investigated. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1532–1538, 2004     

Hydrophobic cellulose fibers via ATRP and their performance in the removal of pyrene from water

In the present work, cellulose fibers were modified by grafting with poly(lauryl acrylate) and poly(octadecyl acrylate). The grafted materials were prepared by polymerization of the corresponding monomers via surface initiated atom transfer radical polymerization, starting from cellulose papers previously modified with 2‐bromoisobutyryl groups. The polymerizations were carried out in the presence of ethyl‐2‐bromoisobutyrate, as a sacrificial initiator, added to control the molecular weight of the anchored segments, and polymerization kinetics. The grafting of both polymers was confirmed by infrared spectroscopy and elemental analysis. The effect of grafting these polymers on the thermal stability, morphology, and surface properties of cellulose fibers was studied using thermogravimetric analysis, scanning electron microscopy, and measuring water contact angle, respectively. The results reveal that grafting poly(lauryl acrylate) and poly(octadecyl acrylate) to cellulose confers the filter paper a hydrophobic character, and increases its affinity with pyrene, allowing the removal of this pollutant from water. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44482.     

Influence of the COOH and COONa groups and crosslink density of poly(acrylic acid)/montmorillonite superabsorbent composite on water absorbency

A novel poly(acrylic acid)/montmorillonite superabsorbent composite with a water absorbency of 1100 times its own weight was synthesized by the graft copolymerization of acrylic acid with a cross‐linking agent in the presence of montmorillonite ultrafine powder. The influence of the amount of crosslinker and montmorillonite on water absorbency has been investigated. It was found that a crosslinker concentration of 0.03 wt% and 30 wt% montmorillonite gave the best results. The collaborative absorbent effect of sodium carboxylate and carboxylic acid groups was superior to that of sodium carboxylate or carboxylic acid groups alone, and the composite with a ratio of about 2/3 for sodium carboxylate to carboxyl acid groups possessed the highest water absorbence. © 2001 Society of Chemical Industry     

Controlled‐release polymers for delivery of dipyridyls and tetraalkyl ammonium hydroxide

A method to incorporate 2,2′‐(or 4,4′‐)dipyridyl and tetra‐n‐butylammonium hydroxide into poly(vinyl alcohol) (PVA) monoliths and the controlled‐release properties of these polymer monoliths for delivery of the reagents are reported. The monoliths were prepared by heating PVA beads until they formed a viscous liquid and then loading the molten polymers with the desired reagents. Several freeze‐thaw cycles were then carried out to provide the mechanically stable, reagent‐loaded monoliths. The release of the reagents from the PVA monoliths was monitored by UV–vis spectroscopy, and the release was found to proceed in a controlled manner, yielding consistent results among different reagent‐loaded PVA monoliths. In addition, the reagents underwent no chemical changes upon their release from the monoliths. Limitations of the use of the controlled‐released chemicals as replenished reagents in Fujiwara reactions for the continuous monitoring of halocarbons are discussed. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1043–1048, 2007     

Structure‐property and swelling behavior of electron beam irradiated poly(vinyl alcohol)/acrylamide/sodium montmorillonite clay composites

Composites based on poly(vinyl alcohol) (PVA), acrylamide monomer (AM) and sodium montmorillonite clay (MMT) were prepared, in the form of thin films, by solution casting. The PVA/AM/MMT composites films were then exposed to electron beam irradiation to form crosslinked network structure. The structure‐property behavior of PVA/AM/MMT hybrids was demonstrated by x‐ray diffraction (XRD), scanning electron microscopy, gel content, color intensity, thermogravimetric analysis (TGA) and swelling behavior in aqueous solutions. The results indicated that the introduction of MMT clay ratio up to 5% decreased the gel content of PVA/AM hydrogels. The color measurements indicated that the introduction of MMT clay ratio up to 5% was shown to affect the color intensity of composite films. It was found that both PVA/AM hydrogels and PVA/AM/MMT composites reached the equilibrium swelling state in water after four hours; however PVA/AM/MMT composites displayed higher swelling than PVA/AM hydrogels. However, the swelling of PVA/AM hydrogels or their composites at the equilibrium state increased with increasing temperature up to 60°C. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Removal of paraquat pesticide from aqueous solutions using a novel adsorbent material based on polyacrylamide and methylcellulose hydrogels

This research studied the characteristics of poly(acrylamide) and methylcellulose (PAAm‐MC) hydrogels as a novel adsorbent material for removal of pesticide paraquat, from aqueous solution, with potential applications in curbing environmental risk from such herbicides. PAAm‐MC hydrogels with different acrylamide (AAm) and MC concentrations were prepared by a free‐radical polymerization method. The capability of the hydrogels in removing paraquat dichloride from aqueous solution was determined using UV–Vis analysis. The scanning electron microscopy method was used to study the morphological properties of the hydrogels, and swelling degree (Q) of the hydrogels was also measured. The entrapped MC in PAAm chains provoked significant changes in morphological, hydrophilic, and adsorption properties of the PAAm‐MC hydrogels. The adsorption capacity of hydrogels was strongly influenced by AAm, MC, and paraquat concentrations with the highest adsorption capacity (q_eq = 14.3 mg g^?1) was observed for hydrogels synthesized with 6.0% AAm with 0.75% MC swollen in 45.7 mg L^?1 of paraquat solution. Freundlich model performed better than Langmuir model in describing the adsorption isotherm of PAAm‐MC/paraquat system, implying a heterogeneous surface. These results suggest that PAAm‐MC hydrogels are potentially viable absorbents for removal of paraquat pesticide from aqueous solution and cleaning water contaminated with dyes, heavy metals, and others pesticides. © 2009 Wiley Periodicals, Inc. Journal of Appl Polym Sci, 2009     

纤维素/聚乙二醇/维生素共混膜的制备与缓释性能研究

介绍了在纤维素/聚乙二醇体系中加入维生素C制备成药物缓释膜的过程,并研究了其在水中的药物缓释性能。结果表明,固液比、pH和温度这三个条件都对药物缓释有非常明显的影响。例如,药物在中性条件下的缓释一般是随着固液比的增大和温度的升高而加快的,但在高分子材料的结晶温度区域进行时也受到抑制。此外,在酸性环境中药物缓释在初始时是受到抑制而后逐渐以脉冲式进行。值得指出的是,药物缓释在碱性条件下完全不发生,并出现与缓释相反的吸附现象。     

Influence of microwave heating on the kinetic of acrylic acid polymerization and crosslinking

Kinetics of isothermal formation of poly (acrylic acid) (PAA) hydrogels through polymerization of acrylic acid and crosslinking of the PAA formed in a conventionally heated reaction system and in a microwave heated reaction system were investigated. It was found that in the microwave heated system the reaction rate constant of PAA hydrogel formation significantly increased (from 32 to 43 times) when compared with the conventionally heated system. The isothermal kinetics of the PAA hydrogel formation during the microwave process could be described by the so‐called first‐order chemical reaction kinetics model. In contrast, the so‐called second‐order chemical reaction rate model could best describe the isothermal kinetics of the PAA hydrogel formation during the conventionally heated process. Also, in the microwave heated system, the reaction kinetics of the PAA hydrogel formation and its kinetic parameters changed, that is, the activation energy (E_a) decreased by about 19% and the pre‐exponential factor (lnA) decreased by 2.2 times. The decrease in activation energy, change in entropy of activation energy, and decrease in the pre‐exponential value of PAA hydrogel formation under microwave heating are caused with increased energy of the reactive species when compared with their energy in thermal activation. Increased energy of the reactive species is a consequence of rapid transfer and absorption of the energy of microwave field to the existing reactive species. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Control of pore generation and pore size in nanoparticles of poly(styrene‐methyl methacrylate‐acrylic acid)

Seeded emulsion polymerization of styrene‐methyl methacrylate‐acrylic acid onto seed latexes of monodisperse particles of poly(styrene‐methyl methacrylate) was conducted with or without divinyl benzene as a crosslinking agent. Experiments revealed that almost no new particles were formed during the second stage of polymerization, and that the seeded latex particles obtained were almost monodisperse. An alkali‐acid treatment was then applied to the seeded latex particles swollen in 2‐butanone. Experimental results indicated that: (1) for uncrosslinked particles, an optimum volume expansion of >50% is reached for a ratio of the swelling agent, 2‐butanone, to polymer (methyl‐ethyl‐ketone/polymer by weight) between 2.0 and 2.9; the volume expansion is much lower outside the above range. (2) For crosslinked particles, the particle volume expansion follows the same pattern, but with smaller values. (3) pH plays an important role in pore generation and volume expansion. Pore generation is optimized by decreasing pH to a value as low as 1.5 during acid treatment, and by keeping pH in the optimum range between 11.98 and 12.20 during alkali treatment. Based on the above observations, a discussion regarding the mechanism of pore generation and particle expansion is provided. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 72: 419–426, 1999     

Synthesis of diblock and triblock copolymers from butyl acrylate and styrene by reverse iodine transfer polymerization

Well‐defined AB and BA diblock copolymers were obtained by a one‐pot two‐step sequential block copolymerization by reverse iodine transfer polymerization (RITP), A being a poly(styrene) block and B a poly(butyl acrylate) block. High monomer conversions during the formation of the first block avoided the purification steps before growing the second block. In a third sequential step, the diblock copolymers were further extended to synthesize ABA and BAB triblock copolymers. Furthermore, the synthesis of ABA and BAB copolymers in only two steps by RITP was investigated starting with the formation of the central block using 2,5‐di(2‐ethylhexanoylperoxy)‐2,5‐dimethylhexane as a difunctional initiator and then resuming the polymerization to grow the external blocks in a second step. The obtained copolymers were analyzed by size exclusion chromatography, transmission electron microscopy, and differential scanning calorimetry. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of non-uniform initial drug concentration distribution on the kinetics of drug release from glassy hydrogel matrices

The effect of non-uniform initial drug concentration distribution, on the kinetics of drug release from polymer matrices has been examined theoretically. The results indicate that a constant-rate of drug release can be achieved, via a specific sigmoidal drug concentration distribution without the need to have a saturated drug reservoir as in a membrane-reservoir system. To test this concept, a novel approach has been developed, which utilizes the non-Fickian swelling behaviour in glassy hydrogels to develop an inflection-point containing drug concentration profile, followed by a freeze-drying step to rapidly remove the swelling solvent and immobilize in-situ the desired sigmoidal drug concentration distribution. The drug release from such a system generally exhibits a characteristic time-lag and a constant-rate release region similar to that of a membrane-reservoir system. The applicability of the present concept and process has been demonstrated experimentally with the release of oxprenolol HCl from hydrogel beads; based on 2-hydroxyethyl methacrylate polymerized with a polymeric crosslinking agent.     

Removal of Poly Aromatic Hydrocarbons (PAHs) from Water: Effect of Nano and Modified Nano-clays as a Flocculation Aid and Adsorbent in Coagulation-flocculation Process

Water treatment process involving simultaneous action of adsorption on different nano and organo-modified nano-clays followed by coagulation-flocculation by alum and poly aluminium chloride (PAC) has been evaluated for the removal of PAHs (naphthalene, acenaphthalene, phenanthrene, fluoranthene, anthracene, and pyrene) from water. When clay minerals along with alum and PAC were used for treatment, 37.4–100.0% removal of PAHs was observed compared to 20–38% removal using normal water treatment process with either alum or alum + PAC. The effectiveness of clay minerals for removal of PAHs followed the order (P < 0.05): halloysitenano-clay (HN-clay) < normal bentonite (NB-clay) < hydrophilic nano-bentonite (HNB-clay) < nano-montmorillonite modified with dimethyl dialkyl amine (DMDA-M-clay) ≈ nano-montmorillonite modified with octadecylamine and aminopropyltriethoxysilane (ODAAPS-M-clay) ≈ nano-montmorillonite modified with octadecylamine (ODA-M-clay) in combination with alum + PAC. The modified treatment process (alum + PAC + clay minerals), where water was initially treated with clays followed by normal process of coagulation (alum + PAC), was found to be the most effective method with maximum removal for ODAAPS-M-clay (97.7–100.0%) which is at par wih ODA-M (97.0–100.0%), and DMDA-M-clay (94.8–100%). The removal of PAHs varied in the order: naphthalene ≈ acenaphthalene > anthracene ≈ pyrene > phenanthrene > fluoranthrene. The treatment combination having the maximum removal capacity was also used eficiently for the removal of PAHs from natural and fortified natural water. This article demonstrated adsorption-coagulation integrated system has the potential to remediate PAHs polluted water.     

Swelling and drug release profile of poly(2‐ethyl‐2‐oxazoline)‐based hydrogels prepared by gamma radiation‐induced copolymerization

Poly(2‐ethyl‐2‐oxazoline) and acrylic acid were copolymerized in different compositions using γ‐rays‐induced polymerization and cross‐linking to obtain a series of pH‐sensitive hydrogels. The preparation parameters that may affect the copolymerization process such as the feed solution composition and irradiation dose were optimized. Swelling characteristics of the obtained polymeric hydrogels were evaluated. The results show the significant effects of the hydrogel composition, soaking time, and pH on the swelling equilibrium. The diffusion parameters obtained at pH 1 and 7 show the possibility of using the prepared hydrogels in the field of colon‐specific drug delivery systems. Ibuprofen as a model drug was loaded into (poly(2‐ethyl‐2‐oxazoline)/acrylic acid) copolymer hydrogel to investigate their drug release behavior at different pH values. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

硫酸生产废水治理与双水闭路循环系统

介绍硫酸生产中,酸性含砷废水的治理方法,及双水闭路水循环系统的流程、运行情况与经济效益。含砷10mg/L以下,仅用石灰一级中和沉降后,出水即可达标;含砷10～20mg/L需用石灰、FeSO4二级处理方可达标。双水闭路循环投入运行,开车率100%,实现了硫酸生产废水的零排放,产生数十万元的经济效益。     

Synthesis and functionalization of nanoengineered materials using click chemistry

The synthesis of nanoengineered materials with precise control over material composition, architecture and functionality is integral to advances in diverse fields, including biomedicine. Over the last 10 years, click chemistry has emerged as a prominent and versatile approach to engineer materials with specific properties. Herein, we highlight the application of click chemistry for the synthesis of nanoengineered materials, ranging from ultrathin films to delivery systems such as polymersomes, dendrimers and capsules. In addition, we discuss the use of click chemistry for functionalizing such materials, focusing on modifications aimed at biomedical applications.     

Atom transfer radical polymerization (ATRP): A versatile and forceful tool for functional membranes

The progress in atom transfer radical polymerization (ATRP) provides an effective means for the design and preparation of functional membranes. Polymeric membranes with different macromolecular architectures applied in fuel cells, including block and graft copolymers are conveniently prepared via ATRP. Moreover, ATRP has also been widely used to introduce functionality onto the membrane surface to enhance its use in specific applications, such as antifouling, stimuli-responsive, adsorption function and pervaporation. In this review, the recent design and synthesis of advanced functional membranes via the ATRP technique are discussed in detail and their especial advantages are highlighted by selected examples extract the principles for preparation or modification of membranes using the ATRP methodology.