Partial characterization of white cabbages (Brassica oleracea var. capitata f. alba) from different regions by glucosinolates, bioactive compounds, total antioxidant activities and proteins

Glucosinolates (GLS), antioxidative compounds, total radical scavenging activities (TRSAs) and proteins of white cabbage samples derived from different regions of Europe, collected in the spring and autumn, were studied. Glucobrassicin and sinigrin were the dominating GLS in all analyzed cabbage samples. Depending on origin, these two GLS accounted for ∼30% to ∼70% of the total. The total GLS content ranged from 3.3 to 7.7 μmol/g dw in lyophilized vegetables. Assays based on electron transfer [total phenols by Folin-Ciocalteu reagent (FCR), 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid)] radical cation (ABTS) and 1,1-diphenyl-2-picrylhydrazyl (DPPH)] were used to compare the TRSAs and the main bioactive compounds in cabbage. Total polyphenols varied from 2.4 to 4.9 GAE/g dw. The TRSAs ranged from 2.7 to 8.2 μmol TE/g dw in ABTS test and from 2.4 to 5.4 μmol TE/g dw in DPPH assay. The maximum amount of polyphenol compounds, antioxidant activity, as well as total GLS content, were recorded in Belgian cabbage harvested in the autumn and the lowest ones were found for Poland 2 cabbage harvested in the spring. In extracted and separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) proteins from cabbage leaves only in samples from England and Belgium some differences in patterns were found in the regions of 60 and 97 kDa. The calculated correlations between antioxidative potency and the abundance of bioactive compounds were highly statistically significant. This suggests that TRSA could serve as a means of standardization of natural mixtures, at least in the case of cabbage, necessary to compare results of biological studies carried out for vegetable derived samples.     

Electrodeposition and heat treatment of nickel/silicon carbide composites

Electrodeposited Ni/SiC composite coatings were obtained in a Watts-type bath. The effect of fine SiC particles on polarization curves of the cathodic reduction of nickel ions was discussed. The incorporation of the particles into the deposit with respect to current density and SiC concentration in the bath was tested. Cathodic current efficiencies were also calculated. Structure of as-plated and heat-treated Ni/SiC composites were examined by means of metallography observations as well as scanning and transmission electron microscopy methods. Two phase transformations in the temperatures range of 20-700 °C were found. For annealed samples, Ni₂Si and Ni₃Si₂ phases were identified. Hardening of the Ni/SiC composites as a function of the particle content in the deposit and annealing temperature was determined by means of the microhardness testing method.     

Particle emission characteristics of office printers

In modern society, printers are widely used in the office environment. This study investigated particle number and PM2.5 emissions from printers using the TSI SMPS, TSI CPC 3022, and 3025A TSI P-Trak and DustTrak. The monitoring of particle characteristics in a large open-plan office showed that particles generated by printers can significantly (p = 0.01) affect the submicrometer particle number concentration levels in the office. An investigation of the submicrometer particle emissions produced by each of the 62 printers used in the office building was also conducted and based on the particle concentrations in the immediate vicinity of the printers, after a short printing job, the printers were divided into four classes: non-emitters, and low, medium, and high emitters. It was found that approximately 60% of the investigated printers did not emit submicrometer particles and of the 40% that did emit particles, 27% were high particle emitters. Particle emission characteristics from three different laser printers were also studied in an experimental chamber, which showed that particle emission rates are printer-type specific and are affected by toner coverage and cartridge age. While a more comprehensive study is still required, to provide a better database of printer emission rates, as well as their chemical characteristics, the results from this study imply that submicrometer particle concentration levels in an office can be reduced by a proper choice of the printers.     

Exposure to particles from laser printers operating within office workplaces

While recent research has provided valuable information as to the composition of laser printer particles, their formation mechanisms, and explained why some printers are emitters while others are low emitters, questions relating to the potential exposure of office workers remained unanswered. In particular, (i) what impact does the operation of laser printers have on the background particle number concentration (PNC) of an office environment over the duration of a typical working day? (ii) What is the airborne particle exposure to office workers in the vicinity of laser printers? (iii) What influence does the office ventilation have upon the transport and concentration of particles? (iv) Is there a need to control the generation of, and/or transport of particles arising from the operation of laser printers within an office environment? (v) What instrumentation and methodology is relevant for characterizing such particles within an office location? We present experimental evidence on printer temporal and spatial PNC during the operation of 107 laser printers within open plan offices of five buildings. The 8 h time-weighted average printer particle exposure is significantly less than the 8 h time-weighted local background particle exposure, but that peak printer particle exposure can be greater than 2 orders of magnitude higher than local background particle exposure. The particle size range is predominantly ultrafine (<100 nm diameter). In addition we have established that office workers are constantly exposed to nonprinter derived particle concentrations, with up to an order of magnitude difference in such exposure among offices, and propose that such exposure be controlled along with exposure to printer derived particles. We also propose, for the first time, that peak particle reference values be calculated for each office area analogous to the criteria used in Australia and elsewhere for evaluating exposure excursion above occupational hazardous chemical exposure standards. A universal peak particle reference value of 2.0 × 10(4) particles cm(-3) has been proposed.     

Carbon dioxide removal in power generation using membrane technology

Carbon dioxide separation by means of membranes from methane reformed synthesis gas and from semi-closed cycle flue gases has been studied. In the first case, removing carbon dioxide using membrane is more energy consuming than removing it, from the same synthesis gas, using chemical absorption, leading to overall energy conversion efficiency of about 39% for the recuperated-auto thermal reforming (R-ATR) cycle equipped with membrane vs. 45% for the same R-ATR equipped with chemical absorption. With reference to the semi-closed cycle, the net cycle efficiency in the case of membrane removal (42.7%) seems to be not very far from the chemical absorption case (46%). Finally, published data about CO₂ membrane separation specific cost have been analysed, showing that the membrane technology for flue gas application can be competitive with respect to chemical absorption if CO₂ flue gas concentration is higher than 10%.     

Palm oil deodorizer distillate as toughening agent in polylactide packaging films

Polylactide (PLA) is the most used biodegradable and biobased food packaging polymer for rigid containers and films. However, its low ductility is a hurdle for increasing its applications in flexible food packaging. A solution is the use of additives. Palm oil deodorizer distillate (PODC) is revealed to be an excellent additive promoting PLA ductility. PODC is a by‐product of vegetable oil refining, which is available in stable quality and in sufficient amounts. Amorphous PLA/PODC blends had an elongation at break of around 130% and that of semi‐crystalline blends was still around 55% compared to the initial 5% of neat PLA. At the same time the PLA rigidity and high glass transition temperatures were kept. PODC was also a very efficient processing aid, allowing for film blow extrusion. The blends were stable in properties during six months without exudation. They complied with legal norms of Food Contact Materials (EU 10/2011) and induced no sensorial alteration of packed food. Therefore PODC is a very interesting alternative to common plasticizers for the production of flexible PLA packaging films. © 2016 Society of Chemical Industry     

Silicon‐containing heterocyclic polymers and thin films made therefrom

Thin films, in the range of tens of micrometers thickness, have been prepared by casting onto glass plates the chloroform or N‐methylpyrrolidone solutions of polyimides or poly(imide‐amide)s containing silicon and phenylquinoxaline units in the main chain. The polymers have been synthesized by solution polycondensation reaction of aromatic diamines having preformed phenylquinoxaline rings with bis(3,4‐dicarboxyphenyl)dimethylsilane dianhydride or with a diacid chloride resulting from the reaction of this dianhydride with p‐aminobenzoic acid. The polymers were easily soluble in polar aprotic solvents and showed high thermal stability. The free‐standing films exhibited good mechanical properties with tensile strengths in the range of 48–86 MPa, tensile modulus in the range of 1.25–2.22 GPa and elongation at break in the range of 3–37%. Electrical insulating properties of some polymer films were evaluated on the basis of dielectric constant and dielectric loss and their variation with frequency and temperature. The values of the dielectric constant at 10 kHz were in the range of 2.94–3.08 for polyimides and 3.89–4.49 for poly(imide‐amide)s. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3062–3068, 2006     

Electrochemical behaviour of cationic polyelectrolytes at a polarized liquid/liquid interface

The behaviours of several cationic polyelectrolytes (chitosan; polyquaternium-4; diethylaminoethyl dextran; polyquaternium-10, and aminoacrylmethacrylate copolymer, Eudragit^® E100) at a polarised liquid/liquid interface are analysed and compared in the present paper. Based on the analysis of the voltammetric results, it was possible to determine some of the relationships between polymer structure and the tendency to adsorb at the interface. It was also possible to determine the substitution degree of a polymer comprising a chitosan main chain modified with glycidyltrimethylammonium chloride, and the values obtained are in agreement with those calculated using other methodologies. Finally, we report a comparative study concerning the effect of cationic (chitosan) and anionic (dextran sulphate) polyelectrolytes on the compactness of a phospholipid film.     

Structural and photoresponsive behavior of a series of (phenylene)azobenzene‐containing liquid‐crystalline methacrylic copolymers

A series of side‐chain liquid‐crystalline methacrylic copolymers, having various amounts of 4′‐(4‐decyloxyphenyl)‐4‐(hexyloxy)‐azobenzene as the mesogenic group, were synthesized and characterized by differential scanning calorimetry, polarizing optical microscopy and X‐ray diffraction to determine their mesomorphic properties, and by UV?visible spectrometry to elucidate their optical absorption characteristics. Also, birefringence and surface relief gratings were photoinduced in the films using a laser beam of 413 nm. Copolymers with high mesogen contents display a polymorphic behavior of the smectic type. The smectic order tends to disappear as the content of mesogens in the copolymer decreases, going from extended lamellar domains of chromophores packed in a parallel position, typical for smectic liquid crystals, to small aggregates of chromophores dispersed in an amorphous matrix. Important hypsochromic shifts (Δλ_max ≈ 20 nm), associated with π interactions between neighboring aromatic groups, confirm the aggregation of chromophores in lamellar structures. The light‐induced birefringence (0.005 ? 0.06) is not as high as expected but it corroborates that there exists a tight interplay between photoinduced orientation and intrinsic molecular order. Surface relief gratings were recorded in copolymers with low mesogen content (15 ? 30 mol%), showing by atomic force microscopy sinusoidal profiles with an average depth of around 150 nm. © 2013 Society of Chemical Industry