Dual Polymer Conditioning of Water Treatment Residuals

Conditioning of either wastewater biosolids or water treatment residuals conventionally utilizes a single polymer to improve subsequent dewatering. The sequential addition of two polymers has been reported to enhance biosolids dewaterability, but comparable benefits have not been demonstrated for water treatment residuals. This paper evaluated the use of cationic and nonionic polymers, singly and in combination (dual), to investigate whether dual polymer conditioning of residuals offers any advantages, and to determine whether the results could be accommodated by current mechanistic understandings. For this purpose, lab-scale tests used capillary suction time (CST), supernatant viscosity, zeta potential, streaming current, turbidity, floc size, and rheometric analyses. Comparisons of CST and viscosity results for single and dual polymer additions indicated that dual polymer use gave moderately improved dewaterability, possibly due to the increased mixing utilized for dual polymer addition. Using a cationic polymer produced a less turbid supernatant. Zeta potential and streaming current were not good indicators of conditioning efficacy when a nonionic polymer was used. Rheometric analyses were only meaningful in one selected method for treatment of the data: the area under the rheogram up to a shear rate of 30?inverse?s. Overall, implementation of dual polymer use does not appear warranted.     

Using of Photoluminescent Tile for Evacuation of the Buildings During Electrical Failure

Photoluminescent pigments could be successfully applied on the wall tiles, floor tiles and porcelain tiles as well as glass substrates （glass mosaics, borders, and cutted glass with various designs）. For this applications, these products can be used for different purposes. In this study, these pigments are applied on the ceramic tiles and glass mosaics/tiles with traditional ceramic production line. These products are intentended to provide guidance in the event of a power failure. With this study also aimed to prevent potential accidents and injury during evacuation of building.     

Synthesis,structural characterization,and antiproliferative/cytotoxic effects of a novel modified poly(maleic anhydride-co-vinyl acetate)/doxorubicin conjugate

Polymer Bulletin - Drug carrier, poly(maleic anhydride-co-vinyl acetate) (MAVA or poly[MA-co-VA]) copolymer, was traditionally synthesized by free radical chain polymerization reaction, in methyl...     

Microbial profile and bacterial characterisation of naturally debittered Hurma olives compared to non‐debittered Erkence variety during ripening period

Naturally debittered Hurma olive is grown in a specific area in Karaburun peninsula in Turkey. It is characterised by its sweet taste and it differs from other varieties by losing its bitterness caused by phenolic compounds during its maturation period on the tree. Therefore, Hurma olive does not require any further debittering process to be served as table olive. This study was particularly interested in the comparison of the microbial profile of Hurma olive during its 8 weeks of maturation period in two subsequent harvest years and Erkence (not naturally debittered) olive. In addition, main bacterial profile of both Hurma and Erkence olives were isolated and identified. Aerobic mesophilic microorganism (AMM), lactic acid bacteria (LAB), Enterobacteriaceae, Pseudomonadaceae, Staphylococci, Micrococcaceae, yeasts and moulds (Y&Ms) were detected (counted and isolated) in the olive drupes during the maturation period. Isolated bacteria were identified as different spp. of Bacillaceae, Enterobacteriaceae, Micrococcoceae and Pseudomonadaceae.     

Synthesis and polymerizations of novel bisphosphonate‐containing methacrylates derived from alkyl α‐hydroxymethacrylates

The synthesis and polymerizations of four novel bisphosphonate‐containing monomers are reported. The monomers were synthesized from reaction of ethyl and tert‐butyl α‐bromomethacrylates with 3,3‐bis(diethoxyphosphoryl)propanoic acid or with tetraethyl 4‐hydroxybutane‐1,1‐diyldiphosphonate. Their thermal bulk polymerizations, photopolymerizations and copolymerizations with poly(ethylene glycol) methyl ether methacrylate were investigated. The homopolymerizations resulted in polymers with values of 25 000–83 000 g mol^?1; the copolymerizations yielded soluble polymers with 22–34% incorporation of the new monomers; the photopolymerizations gave some structure–reactivity correlation; and one of the homopolymers, upon hydrolysis of its bisphosphonate groups, could interact with hydroxyapatite. © 2013 Society of Chemical Industry     

Properties of biodegradable PVA/sepiolite‐based nanocomposite fiber mats

In this study, poly(vinyl alcohol) (PVA) nanocomposite fiber mats with sepiolite were prepared via electrospinning technique. The measurements of fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), contact angle, scanning electron microscopy (SEM), and atomic force microscopy (AFM) were used for the characterization. The effect of polymer/sepiolite ratio and heat treatment on the properties of samples was investigated. The heat treatment which decreased the solubility of nanofibers and the addition of sepiolite resulted in a decrease in nanofiber diameter, contact angle with water, and water drop spreading rate on the material, and also resulted in an increase in water drop spreading rate inside the material. POLYM. COMPOS., 36:2334–2342, 2015. © 2014 Society of Plastics Engineers     

Synthesis and photopolymerization of novel,highly reactive phosphonated-urea-methacrylates for dental materials

An urea methacrylate (1) and two phosphonated methacrylates (2–3) were synthesized from 2-isocyanatoethyl methacrylate (IEM) and benzyl amine (1), diethyl aminomethylphosphonate (2) and diethyl amino(phenyl)methylphosphonate (3). Their photopolymerization rates are notably higher than commercial monomers, despite the presence of only one double bond. Their polymerization rates follow the order 1 ～ 2 > 3 ～ triethylene glycol dimethacrylate (TEGDMA) > 2-hydroxyethyl methacrylate (HEMA). A tendency toward high crosslinking density during thermal bulk polymerizations, low oxygen sensitivity and high conversions with benzophenone during photopolymerization indicated the importance of hydrogen abstraction/chain transfer reactions. It was found that the addition of the monomers to HEMA significantly increased its polymerization rate, proving their utility as replacements for TEGDMA as reactive diluents for 2,2-bis[4-(2-hydroxy-3-methacryloyloxy propyloxy) phenyl] propane (Bis-GMA). Copolymer systems containing 2 and 3 showed improved T_g values compared to Bis-GMA/TEGDMA systems.     

Determination of important biochemical properties of honey to discriminate pure and adulterated honey with sucrose (Saccharum officinarum L.) syrup

The aims of the present study were to determine biochemical properties of honey samples and to discriminate pure and adulterated honey produced by the standard bee feeding method (control honey), the shaking method (pure blossom honey), and overfeeding (100 kg/colony syrup) with sucrose syrup (adulterated honey). The biochemical properties evaluated were moisture, ash, acidity, hydroxymethylfurfural (HMF), specific sugars (i.e. fructose, glucose, fructose–glucose, sucrose, and maltose), diastase activity, δ¹³C value (honey), δ¹³C value (protein), electrical conductivity, potassium, vitamin C, and proline. Fifteen honey samples were analyzed by discriminant analysis stepwise method. Proline, electrical conductivity and sucrose were found as discriminative characters of samples. Based on these three properties 100% of original group cases (samples) correctly classified in their real group. We found that the honey produced by feeding with 100 kg sucrose syrup per colony contained the sucrose as low as pure blossom honey. Therefore, the sugar (sucrose, fructose and glucose) content of honey cannot be used to distinguish between adulterated (sucrose syrup) and pure blossom honey.     

Minimizing the surface effect of PDMS–glass microchip on polymerase chain reaction by dynamic polymer passivation

Polydimethyl siloxane (PDMS)–glass microchip has a very strong surface effect on polymerase chain reaction (PCR), leading to a very poor PCR yield. In the work reported here, practical dynamic passivation of surfaces of PDMS–glass microchip using polyethylene glycol (PEG) or polyvinylpyrrolidone (PVP) was achieved using a conventional thermocycler. The passivation procedure was cost‐effective and easy to conduct. The effects of polymer molecular weight and polymer concentration on tube PCR efficiency were investigated primarily to prescreen out suitable polymers and polymer concentrations in the PCR mixture. The result from tube PCR indicated that both PEG and PVP could affect the performance of Taq polymerase. A final concentration of 0.025% (w/v) or 0.4% (w/v) polymer in the PCR mixture can enhance the tube PCR, while 1% (w/v) polymer was found to inhibit the reaction. PEG was more effective in tube PCR, although PVP performed better in chip PCR. Instead of employing the polymer directly in the PCR mixture, i.e. the conventional in situ passivation approach, another approach of dynamic passivation by pre‐injecting polymers into the microchip achieved better performance. The efficiency of pre‐passivation was found to follow the order: PVP10000>PVP55000, PEG8000> PEG10000>PEG400. After pre‐passivation with PVP10000, PVP55000 and PEG8000, the PCR efficiency can recover to 93%, 86% and 83%, respectively, of that obtained from tube PCR. Copyright © 2006 Society of Chemical Industry