Controlled conversion of polyacrylamide into polyacrylic acid

Interaction of nitrous acid with aqua solution of poly(acrylamide) gives poly(acrylic acid) in quantitative conversion yields. The reaction proceeds smoothly, with simultaneous evolution of nitrogen, provided that the temperature below 5 °C. The procedure presented provides a versatile route to prepare acrylic acid-acrylamide copolymers in any desired composition, by adjusting molar ratio of nitrous acid. Received: 29 January 1997/Revised: 24 July 1997/Accepted: 6 August 1997     

Occurrence of patulin and 5-hydroxymethylfurfural in apple sour,which is a traditional product of Kastamonu,Turkey

Apple sour is a traditional product of Kastamonu, Turkey. It is consumed by spreading on bread or drinking after diluting with water. The aim of this study was to determine patulin (PAT) and 5-hydroxymethylfurfural (HMF) in apple sour. This study is the first to evaluate the occurrence of PAT and HMF in apple sour. The samples were extracted with ethyl acetate using liquid-liquid extraction technique. PAT and HMF were determined by HPLC with UV detection. PAT was detected in all samples, and the PAT level in 94.9% of samples was found to be equal or greater than the legal limit for juice concentrates. The mean value for PAT was found to be 284 ± 307 μg kg^?1. PAT levels in 13 of 39 samples were in the range of 100 ≤ x < 200 μg kg^?1, two samples were in the range of 0 ≤ x < 50 μg kg ?1 and two samples were in the range of 1000 ≤ x < 1500 μg kg¹. HMF levels of all samples were above the legal limit for solid molasses. The mean value for HMF was found to be 16215 ± 13317 mg kg^?1. HMF levels of 10 of 39 samples were determined to be in the range of 10000 ≤ x < 20000 mg kg^?1, eight samples were in the range of 20000 ≤ x < 30000 mg kg^?1 and only three samples were in the range of 100 ≤ x < 1000 mg kg^?1. There was a significant and inverse relationship between HMF and pH of the samples. These results indicate that consumption of apple sour is a considerable risk in terms of HMF and PAT toxicity.     

Numerical and Optical Analysis of Solar Power Level Adaptable Solar Reactor

Solar energy is an abundant renewable energy resource that can be used to provide high process heat necessary to run thermochemical processes for production of various solar fuels and commodities. In a solar reactor, sunlight is concentrated into a receiver through a small opening called the aperture. However, obtaining and maintaining semiconstant high temperatures inside a solar reactor is a challenge. This is because the incident solar radiation can fluctuate depending on the position of the sun and the weather conditions. For fixed aperture size reactors, changes in incident solar flux directly affect the temperature inside the reactor. This paper presents a novel solar reactor with variable aperture mechanism that is designed and manufactured at our lab. Radiation heat transfer analysis of this reactor concept is studied via Monte Carlo (MC) ray tracing. MC ray tracing module is coupled to a steady-state one-dimensional energy equation solver. Energy equation is solved for the wall and gas, accounting for the absorption, emission, and convection. Incoming direct flux values for a typical day are obtained from National Renewable Energy Lab database. Results show that for a perfectly insulated reactor, the average temperature of the working fluid may be kept appreciably constant throughout the day if aperture diameter is varied between 3 cm and 1.5 cm for incoming fluxes starting with 400 W/m² at 05:12 a.m., reaching peak value of 981 W/m² at noon, and eventually receiving 400 W/m² at 6:58 p.m., which can make the solar reactor run about 13 hr continuously at 1500 K semiconstant temperature.     

Antioxidants alleviate electric field-induced effects on lung tissue based on assays of heme oxygenase-1, protein carbonyl content, malondialdehyde, nitric oxide, and hydroxyproline

In order to test whether antioxidants have beneficiary effects on electric field induced damage, we determined the pulmonary levels of heme oxygenase-1 (HO-1), protein carbonyl content (PCO), malondialdehyde (MDA), nitric oxide (NO) and hydroxyproline (HP) under extremely low frequency (ELF) electric (E) field exposure (50 Hz, 12 kV/m, 7 days/for 8 h/day). While PCO levels significantly increased (p < 0.05), insignificant changes (p > 0.05) were observed in HO-1, MDA, NO and HP levels for electric field exposure groups compared to the control group. We have not observed any significant change in these parameters on the electric field group compared to the group where NAC and EGCG were separately applied along with electric field. However, during our previous studies, we have concluded that NAC and EGCG are potent antioxidants and we believe that new studies should be established by way of setting up different experimental conditions.     

Redox initiation system of ceric salt and α,ω‐dihydroxy poly(dimethylsiloxane)s for vinyl polymerization

The redox system of ceric salt and α,ω‐dihydroxy poly(dimethylsiloxane) is used to polymerize vinyl monomers such as acrylonitrile and styrene to produce block copolymers. The concentration and type of α,ω‐dihydroxy poly(dimethylsiloxane) affects the yield and the molecular weight of the copolymers. The copolymers have about 20°C lower glass‐transition temperatures and much higher contact angle values than of the corresponding homopolymer of vinyl monomers, although the weight percent of α,ω‐dihydroxy poly(dimethylsiloxane) of the copolymers is in the range of 1–2%. © 2006 Wiley Periodicals Inc. J Appl Polym Sci 102: 2112–2116, 2006     

Covalent Immobilization of a α-Amylase onto Poly(methyl methacrylate-2-hydroxyethyl methacrylate) Microspheres and the Effect of Ca2+ Ions on the Enzyme Activity

α-Amylase was covalently immobilized onto poly(methyl methacrylate-2-hydroxyethyl methacrylate) microspheres, which were activated by using either epichlorohydrin (ECH) or cyanuric chloride (C₃N₃Cl₃). The properties of the immobilized enzyme were investigated and compared with those of the free enzyme. For the assays carried out at 25 °C and pH 6.9, the relative activities were found to be 73.0% and 90.8% for epichlorohydrin and cyanuric chloride bound enzymes, respectively. Upon immobilization, the maximum activities were obtained at lower pH values and higher temperatures as compared with the free enzyme. Kinetic parameters were calculated as 2.51 g/L, 28.54 g/L and 15.50 g/L for K_m and 1.67 × 10⁻³ gL⁻¹ min⁻¹ 2.89 × 10⁻⁴ gL⁻¹ min⁻¹ and 1.89 × 10⁻³ gL⁻¹ min⁻¹ for V_max for free, epichlorohydrin and cyanuric chloride bound enzymes, respectively. Enzyme activities were found to be ca. 32.7% for ECH and 41.1% for C₃N₃Cl₃ activated matrices after storage for one month. On the other hand the free enzyme lost its activity completely within 20 days. Immobilization, storage stability and repeated use capability experiments carried out in the presence of Ca²⁺ ions demonstrated higher stability in the presence of these ions. The enzymes immobilized in the presence of Ca²⁺ ions retained 90.6% and 90.8% of the original activities even after 30 days in the case of ECH and C₃N₃Cl₃ activations, respectively. In repeated batch experiments, i.e., 20 uses of the enzyme in 3 days; in the absence of Ca²⁺ ions retentions of 79.2% and 77.1% of the original enzyme activities were observed for ECH and C₃N₃Cl₃ immobilized enzymes, respectively, whereas, in the case of addition of Ca²⁺ ions to the assay medium, these values were enhanced to 95.3% and 92.2%.     

Low molecular weight polyacrylic acid with nitrilodi(methylene-phosphonic acid) chain ends for scale inhibition

Poly(acrylic acid) with molecular weight of 5000 was produced by using 2-aminoethanethiol hydrochloride as chain transfer agent. Amine chain end groups of the resulting polyacrylic acid were transformed into nitrilodi(methylenephosphonic acid) by reacting formaldehyde-phosphorous acid in the presence of hydrogen chloride. ¹H NMR, ³¹P NMR and microanalysis were used for structural analysis.The modified polyacrylic acid had much better calcium carbonate scale inhibition effect than commercial poly(acrylic acid).     

The Use of a Eutectic Mixture of Olive Pomace Oil Fatty Amides to Easily Prepare Sulfated Amides Applied as Lime Soap Dispersants

Sulfated diethanolamides of fatty acids are known to be effective lime soap dispersing agents. However, their preparation from fatty acids via fatty amides requires the use of organic solvents due to the high viscosity of both fatty amides and sulfated fatty amides. This study shows that the preparation of sulfated fatty amides is relatively easy when using olive pomace oil as the raw material. The latter, is converted into sulfated fatty amides by performing the following steps: saponification, hydrolysis, esterification, amidation, and sulfation. In the final step, the mixture obtained has sufficient fluidity, due to its high linoleic acid amide content, to obviate the use of organic solvents, as usually suggested in the literature. Characterization of the product was carried out by chemical analyses, FTIR, ¹³C NMR, GC, and HPLC. It was shown that the yield of the amidation reaction is about 80%, and that of the sulfation reaction can exceed 100% against the pure amide (more than one sulfate group could be linked to one amide molecule). On the other hand, the Borghetty test showed that the product is an effective dispersant with a lime soap dispersing power equal to five.     

A comprehensive study on neutronics of a lead–bismuth eutectic cooled accelerator-driven sub-critical system for long-lived fission product transmutation

The aim of this study is to investigate the high-level waste (HLW) transmutation and fissile breeding potentials of a lead–bismuth eutectic (LBE) cooled accelerator-driven system (ADS) for the various configurations (the target radius, R_T = 10–50 cm and the radial thickness of the sub-critical core, δ_SC = 50–80 cm) and for the various fuel compositions (the fuel volume fraction, VF_F = 10%, 12%, 15% and 20% and the fissile fraction, FF = 10–24%) under sub-critical condition. The long-lived fission products (LLFPs: ⁹⁹Tc, ¹²⁹I and ¹³⁵Cs nuclides) and the uranium mono carbide (UC) ceramic fuel are considered as the HLW and the fissile fuel, respectively. The neutronic calculations have been performed per the incident proton (1000 MeV) with the high-energy Monte Carlo code MCNPX in coupled neutron and proton mode using the LA150 library. The numerical results bring out that the case of R_T = 30 cm, δ_SC = 80 cm, VF_F = 10% and FF = 23% is the optimum configuration and fuel composition, from the energy gain point of view, and has a high neutronic performance for an effective LLFP transmutation and fissile breeding.     

Time-dependent Neutronic Analysis for High Level Waste Transmutation in a Fusion-driven Transmuter

This study presents time-dependent transmutations of high-level waste (HLW) including minor actinides (MAs) and long-lived fission products (LLFPs) in the fusion-driven transmuter (FDT) that is optimized in terms of the neutronic performance per fusion neutron in our previous study. Its blanket has two different transmutation zones (MA transmutation zone, TZ_MA, and LLFP transmutation zone, TZ_FP), located separately from each other. High burn-up pressured water reactor (PWR)-mixed oxide (MOX) spent fuel is used as HLW. The time-dependent transmutation analyses have been performed for an operation period (OP) of up to 10 years by 75% plant factor (η) under a first-wall neutron load (P) of 5 MW/m². The effective half-lives of the MA and LLFP nuclides can be shortened significantly in the considered FDT while substantial electricity is produced in situ along the OP.