PMMA‐multigraft copolymers derived from linseed oil,soybean oil,and linoleic acid: Protein adsorption and bacterial adherence

Synthesis of Poly(methyl methacrylate), PMMA‐multigraft copolymers derived from linseed oil, soybean oil, and linoleic acid PMMA‐g‐polymeric oil/oily acid‐g‐poly(3‐hydroxy alkanoate) (PHA), and their protein adsorption and bacterial adherence have been described. Polymeric oil/oily acid peroxides [polymeric soybean oil peroxide (PSB), polymeric linseed oil peroxide (PLO), and polymeric linoleic acid peroxide (PLina)] initiated the copolymerization of MMA and unsaturated PHA‐soya to yield PMMA–PLO–PHA, PMMA–PSB–PHA, and PMMA–PLina–PHA multigraft copolymers. PMMA–PLina–PHA multigraft copolymers were completely soluble while PMMA–PSB–PHA and PMMA–PLO–PHA multigraft copolymers were partially crosslinked. Crosslinked parts of the PLO‐ and PSB‐multigraft copolymers were isolated by the sol gel analysis and characterized by swelling measurements in CHCl₃. Soluble part of the PLO‐ and PSB‐multigraft copolymers and completely soluble PLina‐multigraft copolymers were obtained and characterized by spectroscopic, thermal, gel permeation chromatography (GPC), and scanning electron microscopy (SEM) techniques. In the mechanical properties of the PHA–PLina–PMMA, the elongation at break is reduced up to ～ 9%, more or less preserving the high stress values at its break point (48%) when compared to PLina‐g‐PMMA. The solvent casting film surfaces were studied by means of adsorption of blood proteins and bacterial adhesion. Insertion of the PHA into the multigraft copolymers caused the dramatic increase in bacterial adhesion on the polymer surfaces. PHA insertion into the graft copolymers also increased the protein adsorption. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

A study on the sorption of NO3− and F− on the carboxymethylated starch‐based hydrogels loaded with Fe2+ ions

Using the principle of geochemistry of fluoride, green and cost effective anion adsorbents were developed for the removal of F^? from water systems. The scheme was further applied for the removal of NO₃^? also. Carboxymethylated starch functionalized through network formation with acrylamide was used as adsorbent, and the resultant hydrogels were loaded with Fe²⁺ ions to generate anchorage for the anions. Sorption of Fe²⁺ was studied as a function of different factors such as time, temperature, pH, and ion strength. The network having the highest Fe²⁺ uptake was loaded with the Fe²⁺ ions under optimum conditions and used for the sorption of F^? and NO₃^?. High efficiency has been observed for F^?, as even up to 100% uptake has been observed within just 10 minutes. The support shows high selectivity for NO₃^?, which was used as anion reference. Thermodynamics of sorption confirms low order and low energy processes. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Surface activity and solubilization of a novel series of functional polyurethane surfactants

Functional polyurethane surfactants (di‐block and tri‐block) were synthesized by addition polymerization of 2,4‐toluenediisocyanate with poly(propylene oxide) and monoallyl‐end‐capped poly(ethylene oxide). The chemical structure of the polyurethane surfactants was confirmed by Fourier transform infrared and ¹H NMR spectroscopy. These polymeric surfactants were found to have excellent surface activity. The lowest surface tension of polyurethane surfactant aqueous solutions could be reduced to 37.6 mN m^?1. All the polyurethane surfactants synthesized had low critical micelle concentrations and could reduce the surface tension even at very low concentration levels (10^?6–10^?5 mol L^?1). The solubilization of toluene in micelles of the synthesized polyurethane surfactants was studied using UV‐visible spectroscopy, and the results showed that they all exhibited good solubilization capacity. Possible solubilization positions of toluene in the micelles are conjectured. Copyright © 2006 Society of Chemical Industry     

复合引发体系制备阳离子絮凝剂在污水处理中的应用研究

采用复合引发体系用甲基丙烯酰氧乙基三甲基氯化铵(DMC)和丙烯酰胺(AM)水溶液共聚制备了阳离子高分子絮凝剂P(DMC-AM).并将其应用于十堰市污水厂废水处理,探讨了其投加量和废水pH对CODCr、浊度、色度去除率的影响.结果表明,当处理的废水pH为7.5,P(DMC-AM)投加质量浓度为8 mg/L时,废水的CODCr去除率达到88%以上,色度和浊度的去除率均达到95%以上.     

对氨基苯甲酸生产废水的树脂吸附预处理

采用超高交联吸附树脂处理芳香两性化合物对氨基苯甲酸(PABA)生产废水,通过静态吸附、动态吸附-脱附实验,研究确定了最佳的吸附-脱附工艺条件。结果表明,在常温和2 BV/h的吸附流量条件下,原废水不用调节pH值,直接经JX-101树脂吸附处理20 BV后,CODC r可从6 000 mg/L左右降至700 mg/L左右,CODC r去除率达88%以上,PABA的吸附去除率达99%以上。采用1 BV 8%氨水溶液 1 BV 4%氨水溶液 2 BV水作脱附剂,在313 K脱附温度和1 BV/h脱附流量的条件下,树脂脱附性能良好。该工艺简单,运行稳定,操作简便,可回收有用物质,有望实现工业化。     

Synthesis and characterization of polystyrene initiated using polymeric peroxide

Polymer peroxides were synthesized by copolymerizing tert‐butyl‐3‐isopropenylcumylperoxide (D‐120) with styrene (St). Exothermic peak at 192.7°C in DSC thermogram indicated that peroxy bonds in D‐120 remained intact during the copolymerizing process. The polymeric peroxide was used to initiate polymerization of St. GPC results showed that polystyrene (PS) initiated by the polymeric peroxides was composed of both linear and branched molecules. In addition, the rheology test showed that PS samples initiated by polymeric peroxide contained branched structure and had lower shear viscosities. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 197–202, 2006     

Study on preparation of protein‐imprinted soft‐wet gel composite microspheres with magnetic susceptibility and their characteristics. I. Preparation and particle morphology

Protein‐imprinted soft‐gel composite microspheres with magnetic susceptibility (MS‐PIGMs) were prepared by inverse suspension polymerization, using Fe₃O₄ particles as magnetically susceptible component, acrylamide (AM) and N,N′‐methylenebisacrylamide (BisAM) as polymeric matrix components, toluene as solvent, and bovine serum albumin (BSA) and lysozyme (Lyz) as templates, respectively. The surface morphology of MS‐PIGMs was observed by environmental scanning electron microscope (ESEM) and scanning electron microscope (SEM). The effects of the kinds and amount of dispersants, stirring rate, the amount and adding methods of initiator, the amount of Fe₃O₄ and monomer concentration on particle morphology of MS‐PIGMs, as well as the effects of crosslinking degree on swelling ratio and particle morphology in wet condition were investigated in detail. ESEM and SEM photographs showed that the resulting MS‐PIGMs were all spheroid form and had large quantity of regularly distributed pores in wet condition, which close in dry condition, and the experimental results indicated that all the affecting factors had obvious effects on particle morphology of MS‐PIGMs. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 684–694, 2006     

Effects of multiple weak interactions on the binding of phenolic compounds by polymeric adsorbents

To investigate the effects of multiple weak interactions on the binding of phenolic compounds by polymeric adsorbents, macroporous polystyrene (PS) resin and PS‐based adsorbents with different hydrogen‐bond acceptor atoms (PS CH₂( OCH₂CH₂)_n OCH₃, n = 0, 1, 2, and 3, denoted as PS‐EG₀, PS‐EG₁, PS‐EG₂, and PS‐EG₃) were prepared. The phenol adsorption strength order on these adsorbents was PS/PS‐EG₀ < PS‐EG₁ < PS‐EG₂ < PS‐EG₃, indicating that the adsorption on PS and PS‐EG₀ was driven by hydrophobic and π–π interactions, and the adsorption on PS‐EG₁, PS‐EG₂, and PS‐EG₃ was driven by a hydrogen bond in addition to hydrophobic and π–π interactions. PS‐EG₂ may adsorb a second phenol molecule on each binding site and PS‐EG₃ may adsorb second and third ones. The adsorption strength of resorcinol increased in the order of PS, PS‐EG₁, and PS‐EG₂, indicating that the adsorption was driven by 0, 1, and 2 hydrogen bonds in addition to hydrophobic and π–π interactions. Similarly, the adsorption of phloroglucinol on PS, PS‐EG₁, PS‐EG₂, and PS‐EG₃ was driven by 0, 1, 2, and 3 hydrogen bonds in addition to hydrophobic and π–π interactions because the adsorption strength increased in this order. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4652–4658, 2006     

Titania pigment particles dispersion in water-based paint films

The distribution of titanian pigment, in dry water-based paint films in the presence of polymeric dispeersants containing different functional groups was investigated. The polymeric dispersants chosen were polyacrylic acid and polyacrylamide momo-and copolymers modified with hydroxyl and/or carboxylate groups. Atomic force microscopy (AFM) and transmission electron microscopy (TEM) were used to assess the distribution of the titania pigment particles in the surface and bulk, respectively, of the paint films, which was then compared to the gloss and surface roughnes of these films. In the absence of dispersant, the pigment distribution in the paint film was not uniform and relatively large pigment aggregates appeared at the surface, resulting in a rough surface and low gloss value. All dispersants both decreased surface roughness and increased the gloss of the dry paint film, with the dispersant type considerably enhancing the pigment dispersion in the dry paint film, in agreement with results obtained in aqueous pigment suspensions. In the presence of polyacrylamide homopolymer, the paint gloss increased slightly and further increased with the hydroxyl-modified polyacrylamide copolymer. The paint gloss was highest in the presence of polyacrylic acid or carboxylate/hydroxyl-modified polyacrylamide.     

净水剂的发展和展望

详细讨论了各类净水剂的应用及局限性，提出新型净水剂的研制方向。