Poly(vinyl alcohol)/chitosan/honey/clay responsive nanocomposite hydrogel wound dressing

Many efforts have been made to develop modern wound dressings to overcome limitations of traditional ones. Smart nanocomposite hydrogels are appropriate candidates. In this work, a novel responsive nanocomposite hydrogel based on poly(vinyl alcohol)/chitosan/honey/clay was developed and evaluated as a novel wound dressing. The morphology and properties of synthesized nanocomposite hydrogels loaded with honey as a drug model were investigated. The exfoliated morphology of nanocomposite was confirmed by X‐ray diffractometry. Swelling studies were performed at 20 and 37 °C at various pH. The results showed that swelling increased as a result of temperature rise and maximum swelling occurred at a pH of 2. In vitro release of honey was also studied at the same conditions. Corresponding results indicated faster honey release rate at higher pH values. MTT results exhibited no cytotoxicity in nanocomposite hydrogel system. Investigation of antibacterial activity revealed more than 99% antibacterial activity for proposed system. In vivo results confirmed the wound healing ability of developed system. Generally, appropriate properties of proposed system made it ideal in wound dressing applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46311.     

Preparation of poly(vinyl acetate) latex with ultrasonic and redox initiation

The high water solubility of vinyl acetate (VAc) monomer increases the need for a good initiator system to speed up the polymerization and remove unreacted monomers. Ultrasonic energy can be used to initiate VAc redox emulsion polymerization in the absence of an inert gas and with sodium dodecyl sulfate as a surfactant. Combining ultrasonic energy and a redox initiator at the ambient temperature leads to a higher conversion and higher rate of polymer production in comparison with just using a redox initiator. Ultrasonic energy plays an important role in synthesizing and controlling the polymer structure. The particle size distribution is an important variable in the formulation of latex paint. Ultrasonic energy has an effect on the particle size distribution and average molecular weight of VAc polymer. The particle size increases with an increase in the monomer conversion for ultrasonic polymerization, whereas the particle size stays constant with the monomer conversion for redox polymerization. An ultrasonic polymer has a broader particle size distribution than a redox polymer. The average molecular weight of poly(vinyl acetate) falls with an increase in the sonication time, whereas it increases with time for a redox polymer. Ultrasonic energy also produces a stable, milky white, opaque latex. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 812–817, 2005     

One‐Step Immobilization of Protein‐Encapsulated Core/Shell Particles onto Nanofibers

A novel method is described to functionalize nanofibers to form a nanocomposite with core/shell particles in order to control protein release. The nanocomposite is produced by electrically neutralizing negatively charged poly(lactic acid) nanofibers with positively charged poly[(lactic acid)‐co‐(glycolic acid)] particles via a one‐step electrohydrodynamic jetting process. The protein‐encapsulated core/shell particles exhibited no significant initial burst release or denaturation. The protein release profile was controlled by porosity and protein/polymer interactions. The method may be promising to engineer intelligent scaffolds that can fulfill the needs of biomimetic materials.

     

A new type synthetic filter material for biofilter: Poly(vinyl alcohol)/peat composite bead

In this study, a new type of poly(vinyl alcohol) (PVA)/peat composite bead was prepared and was proved suitable as a filter material in the biofiltration process. The composite bead is a porous spherical particle and has a diameter of 2.4–6.0 mm and a density of 0.69 kg/cm³. It contains 3.25 mg N/g dry solid and 2.91 mg P/g dry solid. The equilibrium moisture content of the composite bead for adsorption and holding experiments is 50.5 and 66.8% by wet basis, respectively. The initial compression strength of the composite bead is 0.32 kg/cm². It has higher moisture holding capacity and compression strength than pig manure compost filter material. The adsorption behavior of ethyl acetate and composite bead follows the Freundlich adsorption isotherm. The composite bead has buffer capacity and could keep the filter bed at pH = 6.9–7.2 during operating. The percentage of removed ethyl acetate was 99% for up to 33 days as the composite bead adsorbed nutrients. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 3248–3255, 2003     

水性核（PMMA）／壳（PU）聚氨酯丙烯酸酯杂化乳液的合成研究

合成高Tg低成膜温度的水性聚氨酯丙烯酸酯杂化乳液,研究了合成工艺、—N CO和—O H的比例、丙烯酸酯含量等因素对乳液稳定性和其他性能的影响。     

种子聚合法制备PS/PAA核壳微球的研究

设计制备了以疏水性聚苯乙烯(PS)为核、以亲水性聚丙烯酸(PAA)为壳的PS/PAA核壳结构复合微球。首先利用无皂乳液聚合法制备了亚微米级的PS微球,再以其为种子,利用种子无皂乳液聚合法制备PS/PAA核壳微球。在种子聚合阶段,选用AIBN当引发剂,经过红外光谱(IR)表征,表明当使用油溶性引发剂偶氮二异丁腈(AIBN),使其最终形成PS/PAA核壳结构微球。这种方法解决了亲水性较强的单体在以水为介质时在PS微球溶于少量的苯乙烯(St),并在引发聚合之前经过充分的吸附溶胀,可使亲水性单体AAc在PS种子微球表面聚合生成壳层,解决表面不容易直接聚合生成壳层的问题。     

Alginate–poly(vinyl alcohol) core–shell microspheres for lipase immobilization

A lipase [triacylglycerol ester hydrolase (EC 3.1.1.3)] was encapsulated in sodium alginate (AlgNa)/poly(vinyl alcohol) (PVA) microspheres. Spherical AlgNa/PVA beads were prepared by the ionotropic gelation of an AlgNa/PVA blend in the presence of calcium tetraborate (CaB₄O₇). The particles were spherical and had an average diameter of 400 μm. The microspheres were studied with differential scanning calorimetry, Fourier transform infrared (FTIR) spectroscopy, and water transport by the equilibrium degree of swelling. The elevation of the glass‐transition temperature of the microspheres indicated specific crosslinking reactions of the component polymers (AlgNa/PVA). FTIR spectra showed no evidence of a strong chemical interaction changing the nature of the functional groups of both AlgNa and PVA in the AlgNa/PVA blends. The water diffusion coefficients increased with increasing PVA content in the microspheres, indicating a decrease in the resistance to mass transfer through the AlgNa/PVA microsphere wall. The AlgNa/PVA microspheres were characterized by the Michaelis constant (K_M) and the maximum reaction velocity (V_max), which were determined for both free and immobilized lipases. The enzyme affinity for the substrate (K_M/V_max) remained quite good after immobilization. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1553–1560, 2006     

Effects of different parameters on the characteristics of chitosan–poly(acrylic acid) nanoparticles obtained by the method of coacervation

Chitosan–poly(acrylic acid) polyelectrolyte complex nanoparticles were prepared by coacervation under mild experimental conditions without the use of any organic solvents or surfactants. The influence of some experimental parameters such as the pH of the polyelectrolyte solutions, their concentrations, and the purification procedure on the particle dimensions and their size distribution was studied in detail. The physicochemical properties of the obtained complex were characterized with Fourier transform infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, and dynamic light scattering. It was found that for solution concentrations below 0.1 wt %, it was possible to obtain suspensions of nanometer‐sized particles. Furthermore, it was established that the pH values of the reactant solutions had a great influence on both the particle size and the yield of the complex that was formed. The most convenient pH values for obtaining chitosan–poly(acrylic acid) particles with a nanometric size and optimum yield (near 90%) were found to be 4.5–5.5 for chitosan and 3.2 for poly(acrylic acid). Additionally, the effects of dialysis and ultrasonic treatment on the stability of complex suspensions, prepared under different experimental conditions, were clarified so that recommendations could be made to bring this system into practical use. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Cadmium and copper absorption mediated by a poly(vinyl alcohol)‐b‐polyacrylonitrile based micelle/Trichosporon cutaneum cell system

The micelles of a recently synthesized copolymer of poly(vinyl alcohol)‐b‐polyacrylonitrile added to the growth solution of the filamentous yeast Trichosporon cutaneum strain R57 led to the formation of a binary system consisting of micelles and cells. The resulting micelle/cell system was studied as a model for the removal of toxic concentrations of heavy‐metal ions (cadmium and copper) from aqueous solutions. The ion‐removal efficiency mediated by this system was higher than for free‐floating cells. The copper‐removal efficiency from the solution reached a level of 65% after 24 h of cultivation, whereas the cadmium‐removal efficiency reached 62% after 6 h of growth. For comparison, the free‐floating cells removed 42% of copper and only 38% of cadmium from the solutions. The effects of surface interactions between the cells and polymer micelles on the biosorption capacity of the cells are discussed in the article. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

核壳结构纳米TiO_2/PU/PMMA复合材料制备及其光催化性能研究

采用纳米TiO2有机化改性、加成及原位乳液聚合,制备了纳米TiO2、聚氨酯(PU)、聚丙烯酸酯(PMMA)的复合材料。透射电镜形貌表明:合成了以纳米TiO2为核,PU与PMMA为壳的核壳结构的复合材料。研究了该复合材料的光催化性能。     

具有硬核—软壳结构的丙烯酸聚合物乳液的研究

利用种子乳液聚合法合成了具有硬核—软壳结构的丙烯酸聚合物微粒子,通过对种子粒子数和最终粒子数的理论计算,并结合最低成膜温度(MFT)的测试结果,描述了聚合物微粒子的聚合过程,同时,还对聚合物乳液的各项性能进行了研究。     

PB—g—PMMA核壳粒子的合成及其在PVC中的分散

聚丁二烯(PB)橡胶粒子与聚氯乙烯(PVC)不相容。采用乳液聚合手段，在聚丁二烯乳胶粒表层接枝与聚氯乙烯相容的聚甲基丙烯酸甲酯(PMMA)充当增容剂制备了聚丁二烯接枝聚甲基丙烯酸甲酯(PB-g-PMMA，MB)核壳粒子。用熔融共混法制备了PVC／MB共混物。SEM照片表明，这种核壳结构的粒子在聚氯乙烯中的分散情况随着核壳比的不同而改变，当核壳质量比小于93／7时能够完全均匀地分散在：PVC基体中，核壳质量比大于94／6时根本不能分散在PVC基体中，核壳质量比为93／7是粒子能否分散开的转折点。共混物的力学性能数据表明，当MB加入量改变时，共混物也存在脆韧转变点，但受MB粒子的核壳比影响。     

皮革涂料用丙烯酸酯核-壳乳液的研制

采用种子乳液聚合法，以交联型软性聚合物为核，交联型硬性高聚物为壳，合成了具有优异耐寒性及高温抗回粘性聚合物。讨论了乳化剂种类及应用、核／壳比等对聚合物性能的影响。     

Synthesis of Co3O4/Poly(N‐vinylcarbazole) Core/Shell Composite With Enhanced Optical Property

Co₃O₄/poly(N‐vinylcarbazole) (PNVC) composite with enhanced optical property was synthesized via a simple in situ bulk polymerization of NVC monomers in the presence of Co₃O₄ nanoparticles at an elevated temperature. High‐resolution electron microscopic observations showed that the Co₃O₄ nanoparticles were coated with uniform nanolayer shells of PNVC. Fourier‐transform infrared (FT‐IR) spectroscopy revealed the presence of strong interactions between the PNVC polymer chains with the Co₃O₄ surface in the Co₃O₄/PNVC composite. Raman spectroscopic results supported conclusions based on electron microscopy and FT‐IR spectra. The uniform nanolayer coating of PNVC decreases the inherent bulk conductivity of Co₃O₄, however, significantly increases the fluorescence property of Co₃O₄ nanoparticles.

     

具有核壳结构的聚苯胺/二氧化硅微球的制备与表征

利用原位聚合(In-situ)方法,在二氧化硅微球表面上成功包覆了聚苯胺层.透射电镜(TEM)照片显示,微球呈现良好的核壳结构,大部分粒径在500 nm左右;包覆后,聚苯胺的红外特征吸收峰发生了红移,表明二氧化硅与聚苯胺两相之间不是简单的物理包覆,而是存在类似于共价键的缔合作用.热重(TG-DTG)曲线显示聚苯胺/二氧化硅微球具有3个明显的失重阶段,并且无机二氧化硅提高了聚苯胺的氧化分解温度.     

Intramolecular and intermolecular crosslinked poly(vinyl alcohol)–borate complexes for the sustained release of fertilizers and enzymes

Therapeutic agents or agricultural fertilizers captured in polymer colloids (PCs) give rise to interesting applications, which are typically related to sustained release. We synthesized crosslinked polymer structures with poly(vinyl alcohol) (PVA) and borax precursors. Fourier transform infrared spectroscopy showed that a polymer–boron ion complex was formed with the crosslinking reaction at the O H site of PVA; thereby, PCs were formed. Field‐emission scanning electron microscopy showed that a uniform mesoporous two‐dimensional structure formed via intermolecular and intramolecular crosslinking. Trypsin enzyme and phosphate fertilizer were trapped in these PCs independently to study sustained release. Fertilizer‐incorporated PCs were mixed with soil samples, in which seeds of fenugreek were sown, and the plant growth was monitored a duration of 15 days. The fertilizer release, studied with UV–visible spectroscopy, showed a sustained signature of the fertilizer (at 690 nm) in the water extracts of soil, with much healthier plant growth compared to the control. For the trypsin‐incorporated PC samples, the released enzyme was made to interact with bovine serum albumin protein to monitor the released percentage with UV absorption spectroscopy. A systematic increase in the enzyme signature (at 280 nm) was observed for a duration of 60 min; this indicated the potential of PC for sustained drug release. The swelling calculations predicted that the mechanism involved was composed of pseudo‐swelling behavior. We envisaged that the hydroxyl groups of the PC broke in water and formed a complex with water. This complex slowly dissolved in water to release the entrapped molecules. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

聚乙烯醇-甲醛-脲三元共聚物的合成及其粘接性能的研究

本文研究了聚乙烯醇-甲醛-脲在酸性介质中的共聚反应，三元共聚物的粘接性能及影响因素。     

Synthesis and characterization of poly(butyl acrylate)/silica and poly(butyl acrylate)/silica/poly(methyl methacrylate) composite particles

Poly(butyl acrylate)/poly(methyl methacrylate) (PBA/PMMA) core–shell particles embedded with nanometer‐sized silica particles were prepared by emulsion polymerization of butyl acrylate (BA) in the presence of silica particles preabsorbed with 2,2′‐azobis(2‐amidinopropane)dihydrochloride (AIBA) initiator and subsequent MMA emulsion polymerization in the presence of PBA/silica composite particles. The morphologies of the resulting PBA/silica and PBA/silica/PMMA composite particles were characterized, which showed that AIBA could be absorbed effectively onto silica particles when the pH of the dispersion medium was greater than the isoelectric potential point of silica. The critical amount of AIBA added to have stable dispersion of silica particles increased as the pH of the dispersion medium increased. PBA/silica composite particles prepared by in situ emulsion polymerization using silica preabsorbed with AIBA showed higher silica absorption efficiency than did the PBA/silica composite particles prepared by direct mixing of PBA latex and silica dispersion or by emulsion polymerization in which AIBA was added after the mixing of BA and silica. The PBA/silica composite particles exhibited a raspberrylike morphology, with silica particles “adhered” to the surfaces of the PBA particles, whereas the PBA/silica/PMMA composite latex particles exhibited a sandwich morphology, with silica particles mainly at the interface between the PBA core and the PMMA shell. Subsequently, the PBA/silica/PMMA composite latex obtained had a narrow particle size distribution and good dispersion stability. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3425–3432, 2006     

Emulsion grafting of vinyl acetate onto preirradiated poly(3‐hydroxybutyrate) film

Vinyl acetate (VAc) was grafted onto poly(3‐hydroxybutyrate) film by a preirradiation method. Grafting reactions were carried out in VAc/water/surfactant emulsion, VAc/water, and VAc/methanol systems. For emulsion grafting, Nonion L‐4 was ascertained to be the optimum surfactant with respect to the stability of a single emulsion layer. The emulsion with a 10 : 1 (w/w) ratio of VAc to surfactant yielded the highest degree of grafting: 23%. The grafting efficiency in the emulsion and the water and methanol solvents were evaluated. The results indicated that the grafting efficiency of the emulsion was 100 times that of VAc/methanol when the same 2 wt % VAc was used in the grafting reaction. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008