Synthesis and flocculation properties of poly(diallyldimethyl ammonium chloride–vinyl trimethoxysilane) and poly(diallyldimethyl ammonium chloride–acrylamide–vinyl trimethoxysilane)

Poly(diallyldimethyl ammonium chloride–vinyl trimethoxysilane) [P(DADMAC–VTMS)] and poly(diallyldimethyl ammonium chloride–acrylamide–vinyl trimethoxysilane) [P(DADMAC–AM–VTMS)], the latter a new cationically charged and hydrophobically modified flocculant, were obtained by radical polymerization initiated by potassium persulfate. The effects of the vinyl trimethoxysilane (VTMS) feed ratio on the intrinsic viscosity and solubility of the polymers were examined. The effects of the flocculants on turbidity removal, decolorization, and oil removal in water treatment were also studied. The introduction of VTMS increased the intrinsic viscosities of P(DADMAC–VTMS) and P(DADMAC–AM–VTMS) in comparison with the viscosities of poly(diallyldimethyl ammonium chloride) and poly(diallyldimethyl ammonium chloride–acrylamide), respectively, but reduced their solubilities. The introduction of VTMS also enhanced the flocculation properties of P(DADMAC–VTMS) and P(DADMAC–AM–VTMS), including turbidity removal, decolorization, and oil removal. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 335–342, 2002; DOI 10.1002/app.10339     

离子液体-TiO_2体系选择性催化降解染料废水的研究

将离子液体和TiO_2P25纳米颗粒物理掺杂,构建了具有选择性降解功能的离子液体-TiO_2复合光催化体系,实现了染料废水的选择性降解。研究发现,离子液体的加入能够提高TiO_2对阴离子染料的降解效率,抑制阳离子染料的降解。通过优化离子液体的结构、用量等因素,筛选出了最佳复合体系[C_(10)mim](CF_3SO_2)_2N-TiO_2P25(物质的量比为20∶1)。紫外光照射下,20 min即可将10.0 mg/L甲基橙溶液几乎脱色完全,而对阳离子染料的降解几乎完全抑制。该体系可以选择性地降解染料废水中的某一组分,简化阴阳染料的分离和回收。     

Synthesis,characterization, and flocculation properties of poly(acrylamide‐methacryloxyethyltrimethyl ammonium chloride‐methacryloxypropyltrimethoxy silane)

A novel hydrophobically modified and cationic flocculant poly(acrylamide‐methacryloxyethyltrimethyl ammonium chloride‐methacryloxypropyltrimethoxy silane) (P(AM‐DMC‐MAPMS)) was synthesized by inverse emulsion polymerization. The molecular structure of hydrophobically cationic polyacrylamide (HCPAM) was characterized by FTIR and ¹H‐NMR. The effects of DMC and MAPMS feed ratio on intrinsic viscosity and solubility were measured. The effects of hydrophobically cationic flocculants on reactive brilliant red X‐3B solution and kaolin suspension were studied. It was found that the introduction of MAPMS could increase the intrinsic viscosities of P(AM‐DMC‐MAPMS) and enhance the flocculation properties to anionic dye solution and kaolin suspension, but reduced their water‐solubility. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Decolorization of textile dyes by Bjerkandera sp. BOL 13 using waste biomass as carbon source

BACKGROUND: Phanerochaete chrysosporium, Trametes versicolor and Bjerkandera sp BOL13 were compared for decolorization of azo dyes supplied individually or as a mixture. The dye decolorization was also evaluated during continuous treatment under non‐sterile conditions using a lignocellulosic growth substrate. RESULTS: Bjerkandera sp BOL13 showed the highest dye decolorization potential. This fungus was also found to support high decolorization of Remazol Red RR at an initial pH of 4‐6 and when using straw as co‐substrate. The fungus was evaluated for Remazol Red RR decolorization in a continuously fed packed‐bed bioreactor operated under non‐sterile conditions with 3 days of hydraulic retention time. When glucose was supplied as growth‐substrate, decolorization efficiencies of 65‐90% were maintained for 12 days in a bioreactor packed with wooden material. The decolorization efficiency was lower when glucose was not fed to the fungus or when a plastic material was used as packing. Higher manganese peroxidase and laccase activities were also recorded when the wood packing was used. Contamination caused a drop in decolorization efficiency after 17‐19 days operation. CONCLUSIONS: The potential of Bjerkandera sp BOL13 for decolorization of azo dyes under non‐sterile conditions using lignocellulosic growth substrates was demonstrated. Research is needed to reduce contamination under non‐sterile conditions. © 2012 Society of Chemical Industry     

Synthesis of perfluorohexyl‐terminated poly(ethylene oxide) using maghnite‐h as clay catalyst

Activated monomer cationic ring‐opening polymerization of ethylene oxide initiated with 1H,1H,2H, 2H‐perfluorooctan‐1‐ol, using acid exchanged montmorillonite clay called Maghnite‐H⁺ (Mag‐H⁺) as an effective catalyst, was carried out to obtain the corresponding homopolymers with narrow polydispersity ratios. The molecular weights of the obtained polymers could be controlled with the feed ratio of the monomer and initiator. The effect of amount of catalyst and time on the polymerization yield and viscosity of the polymers were studied. The structure was confirmed by ¹H‐NMR and MALDI‐TOF‐MS. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Photocatalytic decolorization of Basic Blue 41 using TiO2-Fe3O4-bentonite coating applied to ceramic in continuous system

Abstract

Photocatalytic degradation/decolorization of Basic Blue 41 dye assisted by UV radiation has been studied over TiO₂-Fe₃O₄ supported by bentonite. In this experiment, photocatalytic decolorization process was performed continuously; where dye feed solution was supplied to a coated-ceramic vessel. The influence of the initial concentration, pH, and flow rate of the dye feed solution on the degradation efficiency process was examined in this study. The results showed that the increase in the dye concentration and flow rate reduces decolorization efficiency. The highest decolorization efficiency was at pH of 5.5. The kinetic study of this photo-decolorization indicated that under the experimental condition, the photocatalytic kinetic process followed first-order kinetics on the basis of Langmuir–Hinshelwood heterogeneous reaction mechanism, where the reaction rate constant, namely k_r, is 0.7707 and the adsorption rate constant, namely K, is 0.01298.     

Preparation and characterization of vinyltrimethoxysilane and dicumyl peroxide–cured (ethylene propylene diene monomer)/polypropylene thermoplastic vulcanizates

The present investigation deals with understanding the influence of vinyltrimethoxysilane (VTMS) concentration on the mechanical, thermal, thermomechanical, rheological, morphological, gel content, crosslinking density, and compression set properties of dynamically vulcanized ethylene propylene diene monomer (EPDM)/polypropylene (PP) (60/40, w/w) ‐based thermoplastic vulcanizates. It was determined that the values of crosslinking density, gel content, tensile strength, Young's modulus, elongation at break, and viscosity increased; whereas that of compression set, melting temperature, enthalpy of melting, crystallinity, and damping factor decreased with increased addition of VTMS in the EPDM/PP‐based thermoplastic vulcanizate. This is attributed to the physical crosslinking caused because of VTMS grafting on EPDM and chemical crosslinking induced by VTMS between PP and EPDM. This has been confirmed by Fourier‐transform infrared spectroscopy spectra, whereas the thermomechanical and scanning electron microscopy analysis confirmed increased compatibility between EPDM and PP on the addition of VTMS. J. VINYL ADDIT. TECHNOL., 23:312–320, 2017. © 2015 Society of Plastics Engineers     

铝硅酸盐对阳离子染料脱色的研究

研究了粉煤灰合成的铝硅酸盐活性物质对阳离子染料脱色影响的有关因素。结果表明 ,4‰的活性组分能使浓度为 1 0 0 mg/ L的染料废水明显脱色。     

Transport of cationic dye by supported liquid membrane using D2EHPA as the carrier

The transport of cationic dye from an aqueous feed solution through a flat‐type supported liquid membrane containing di‐(2‐ethylhexyl)phosphoric acid as a carrier was studied. The influence of pH on the source phase, the effect of the concentration of the receiving phase, the stirring speed, the effect of the initial dye concentration, the feed‐to‐strip ratio and the influence of the support characteristics were studied. A polytetrafluoroethylene membrane with a 1.0‐μm pore size was found to have more permeability than that with a pore size of 0.5 μm. The results indicated that the aqueous feed solution at an alkaline pH has high permeability. The initial feed phase dye can be completely extracted and stripped with a stripping solution within 7 h.     

Cationic polymerization of ethylene oxide with Maghnite‐H as a clay catalyst in the presence of ethylene glycol

The activated‐monomer cationic ring‐opening polymerization of ethylene oxide, initiated with ethylene glycol and using an acid‐exchanged montmorillonite clay called Maghnite‐H⁺ as an effective catalyst, was carried out to obtain the corresponding homopolymers with narrow polydispersity ratios. The molecular weights of the obtained polymers were controlled with the feed ratio of the monomer to the initiator. The effects of the amount of the catalyst and time on the polymerization yield and viscosity of the polymers were studied. The structure was confirmed with proton nuclear magnetic resonance and matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Microbial Fuel Cell Application for Azoic Dye Decolorization with Simultaneous Bioenergy Production Using Stenotrophomonas sp.

A single‐chamber air‐cathode microbial fuel cell (MFC) was successfully applied for decolorization of the diazoic dye Reactive Black 5 (RB5) with simultaneous production of electricity. An innovative low‐cost medium, the marine water‐glucose‐yeast extract medium (MWGY), was developed which appears as a textile marine effluent in terms of salinity. The anode compartment containing a single bacterial strain of Stenotrophomonas sp. showed almost complete dye decolorization with different RB5 concentrations after seven days of treatment. For the four dye concentrations used, a correlation between dye removal and production of electrical energy was found. The comparison of the decolorization process in the MFC with that in a batch reactor as control experiment highlights the efficiency of the single‐chamber air‐cathode MFC technology which improved the dye removal by the same bacterial strain.     

Bir型氧化锰对阳离子黄X-5GL染料的脱色研究

采用溶胶凝胶法制得Birnessite(Bir)型氧化锰,并对阳离子黄X-5GL的模拟染料废水进行脱色研究。在考察废水处理体系初始pH、Bir型氧化锰用量等影响因素的基础上,进一步考察了Mg2+、Ca2+及重金属离子(Pb2+、Cd2+、Hg2+)对脱色效果的影响。结果表明,Bir型氧化锰对阳离子黄X-5GL具有很好的脱色效果。当pH=2.5、Bir型氧化锰为5 mg时,反应5 min脱色率即达到98%;Mg2+、Ca2+及重金属离子(Pb2+、Cd2+、Hg2+)对脱色效果均无明显影响。pH=2.5时的降解反应近似为一级反应,反应速率常数为0.206 9 min-1。     

P(DMC-AM)对活性染料废水絮凝脱色效果研究

采用混凝烧杯实验,以脱色率为考察指标,研究了系列化阳离子絮凝剂P(DMC-AM)对活性染料废水的絮凝脱色效果和机理。结果表明:P(DMC-AM)阳离子度越大、特征黏度越高、活性染料分子中所含磺酸基数越多,絮凝脱色效果越好,并具有一定耐酸耐盐性。P(DMC-AM)絮凝脱色机理主要为电中和和吸附架桥。实验证明,P(DMC-AM)对活性染料废水具有良好处理效果。     

A new atom transfer radical polymerization initiator based on phenolphthalein for the synthesis of bis‐allyloxy functionalized polystyrene macromonomers

A new atom transfer radical polymerization (ATRP) initiator, namely 2‐(1,1‐bis(4‐(allyloxy)phenyl)‐3‐oxoisoindolin‐2‐yl)ethyl 2‐bromo‐2‐methylpropanoate, was synthesized starting from phenolphthalein, a commercially available and an inexpensive chemical. Well‐ defined bis‐allyloxy functionalized polystyrene macromonomers (M_n,GPC 4800–11 700 g mol^?1) with controlled molecular weight and narrow molecular weight distribution (1.05–1.09) were synthesized using ATRP by varying the monomer to initiator feed ratio. The presence of allyloxy functionality on polystyrene was confirmed by Fourier transform infrared and ¹H NMR spectroscopy. A kinetic study of polymerization revealed pseudo‐first‐order kinetics with respect to monomer consumption. Initiator efficiency was found to be in the range 0.80–0.95. Matrix‐assisted laser desorption ionization time of flight spectra showed a narrow molecular weight distribution with control over the molecular weight. The reactivity of the allyloxy groups on polystyrene was successfully demonstrated by quantitative photochemical thiol‐ene click reaction with benzyl mercaptan as the model thiol reagent. Furthermore, the thiol‐ene click reaction was exploited to introduce other reactive functional groups such as hydroxyl and carboxyl by reaction of α,α′‐bis‐allyloxy functionalized polystyrene with 2‐mercaptoethanol and 3‐mercaptopropionic acid, respectively. © 2014 Society of Chemical Industry     

Gamma radiation on poly(ϵ‐caprolactone) in the presence of vinyltrimethoxysilane

The performance and radiation‐induced cross‐linking of polycaprolactone (PCL) in the presence of vinyltrimethoxysilane (VTMS) have been investigated. Radiation‐induced cross‐linking of PCL in the presence of VTMS followed the Charlesby–Pinner equation, and VTMS promoted the radiation‐induced cross‐linking of PCL. As the concentration of VTMS increased, the gelation dose and the ratio of degradation to cross‐linking (p₀/q₀) decreased and the efficiency of radiation‐induced cross‐linking increased. Differential scanning calorimetry analyses showed differences between the first and second scans. Glass‐transition temperature (T_g) and mechanical properties of the polymers increased. Radiation‐induced cross‐linking of PCL in the presence of VTMS was found to retard hydrolytic degradation greatly. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers     

Hyperbranched polyglycerol/poly(acrylic acid) hydrogel for the efficient removal of methyl violet from aqueous solutions

Hydrogels were synthesized from hyperbranched polyglycerol (HPG) and acrylic acid through free‐radical polymerization with HPG as the crosslinker. The HPG/poly(acrylic acid) (PAA) hydrogel could absorb cationic dyes in aqueous solutions because of the existence of a porous structure and the large numbers of hydroxyl and carboxylic groups. With methyl violet chosen as a model compound, the HPG/PAA hydrogel reached a maximum adsorption of 394.12 mg/g at a feed concentration of 1 g/L. The highest removal ratio of 98.33% was observed at a feed concentration of 50 mg/L. The effects of the pH, contact time, and feed concentration on the dye adsorption were investigated. The dye adsorption data fit well with the pseudo‐second‐order and Langmuir models. We believe that the HPG/PAA hydrogels could perform well in appropriate applications in the removal of cationic dyes from aqueous solutions because of their high adsorption capacity and environmental friendliness. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42951.     

Synthesis,characterization, and rheological studies of methacrylic acid–ethyl acrylate–diallyl phthalate copolymers

Copolymerization of methacrylic acid (MAA) and ethyl acrylate (EA) was performed by the emulsion polymerization technique in the presence of a mixture of ionic and nonionic emulsifiers, at 85°C, using potassium persulfate as initiator (0.16 wt % of monomer). The molar ratio of MAA : EA varied between 44 : 56 and 54 : 46 in the monomer feed. Copolymers of MAA and EA were synthesized by incorporating diallyl phthalate (DAP) with varying concentrations (0–1.7 mol % of total monomer) in the feed. A copolymer latex of MAA, EA, and DAP was also prepared by the variable feed process. The intrinsic viscosity and gel content were determined. Copolymers were characterized by IR and NMR spectroscopic techniques. The composition of copolymers was determined by ¹H‐NMR spectra and sequential distribution from ¹³C{¹H}‐NMR spectra. The pH of the copolymer emulsion varied between 3 and 10 by addition of aqueous ammonia (23% w/w) and its effect on Brookfield viscosity was studied. The effects of copolymer composition, crosslinking agent concentration in the feed, monomer feed process, polymer solid contents, and shear rate on Brookfield viscosity were studied at pH ～ 8. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1430–1441, 2003     

Dye flocculation using polyampholytes and polyelectrolyte‐surfactant nanoparticles

In this article, we report on the dye flocculation performance of polyampholytes containing hydrophobically modified cationic, hydrophilic nonionic, and anionic monomer units, always with an excess of cationic charges. The results are compared with homopolymers and with those obtained using nonstoichiometric polyelectrolyte–surfactant complex (PSC) dispersions with adjustable surface charge density. The polyampholytes as well as the PSC can successfully remove the dye Celliton Fast Blue (Dispers blue 3). The efficiency of dye separation is mainly influenced by the charge of polymers or complexes, demonstrating that charge neutralization is one flocculation mechanism. However, PSC, which are almost neutral, are also able to remove the dye due to their size and structure. In this case, the degree of dye removal is a little bit better and the so‐called flocculation window is broader as in the case of charge neutralization. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1342–1349, 2007     

有机高分子絮凝剂P(DMDAAC-VTMS)和P(DMDAAC-AM-VTMS)的合成及絮凝性能研究

采用水溶液自由基聚合方式,用复合引发剂引发聚合,得到了P（DMDAAC-VTMS）和P（DMDAAC-AM-VTMS）;探讨了BTMS的投料比对聚合物的特性粘度和水溶性的影响;并对这两种絮凝剂的除浊和脱色性能做了初步研究。实验中发现;VTMS的引入使P（DMDAAC-VTMS）和P（DMDAAC-AM-VYMS）的特性粘度分别比PDMDAAC和P（DMDAAC-AM）的特性粘度略微增大,但其水溶性变差;在絮凝性能方面,P（DMDAAC-VTMS）和P（DMDAAC-AM-VTMS）的除浊和脱色性能分别较PDMDAAC和P（DMDAAC-AM）有了提高。     

Grafting of polyelectrolytes onto polyacrylamide by reactive processing

Low‐molecular‐weight high‐charge‐density cationic poly diallydimethyl ammonium chloride (polyDADMAC) was grafted onto nonionic polyacrylamide (PAM) using organic peroxide initiators in the molten state carried out in a batch mixer. The graft copolymer can be used as a high performance flocculant. Glycerol was selected as a plasticizer. The grafting reaction was characterized in terms of composition, temperature, degree of grafting, and grafting efficiency. It was found that free radicals on polymer chains were induced by the decomposition of the initiator. Grafting was produced by free radical recombination termination. The degree of grafting increases with an increase of the polyDADMAC/PAM feed ratio. However, the grafting efficiency was lower than 10 wt % in this highly viscous polymer melt system. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1412–1416, 1999