The effect of volatile organic compounds and hypoxia on paper degradation

The possible effects of volatile organic compounds (VOCs) and of hypoxic conditions on the durability of library and archival collections have been investigated. There is growing evidence that particularly in micro-environments, there may be an important contribution of these indoor-generated pollutants to the degradation of paper. However, since the principal source of VOCs in repositories is the collections themselves, there are also significant possibilities for less stable papers, which are net VOC emitters, to promote the degradation of more stable papers, which may be net VOC absorbers.Using a range of model and real historic papers, the influence of acetic acid, formic acid, furfural, toluene, 1,4-diethylbenzene, iso-butylbenzol, 2-pentylfuran, paraformaldehyde, hexanal and vanillin was evaluated by adding them to samples degraded in closed vessels at elevated temperature. Possible protective effects of the use of activated charcoal cloth, oxygen removal, and of various chemisorbents were also investigated.The results strongly suggest that particularly VOCs with acidic or oxidisable functions can have a strong effect on degradation of cellulose. This is less pronounced in lignin-containing and acidic papers and more pronounced in papers with a small alkaline reserve. The removal of VOCs from the immediate environment can have a pronounced beneficial effect on papers emitting VOCs more intensively, in fact, the lifetime expectancy can be doubled.The results have immediate implications for storage of paper-based heritage in enclosures, but also for initiation of long-term VOC monitoring programmes in libraries and archives, where significant development is still needed.     

Computational probe of cavitation events in protein systems

Previous all-atom simulations have identified several classes of proteins where hydrophobic de-wetting (cavitation) is at play. Here we develop and validate a computationally fast method that predicts in which protein systems water spontaneously cavitates. We implement a cubic lattice model, which incorporates the protein shape from crystallographic data and the protein-water interactions from thermodynamic data. Combining it with the previously developed coarse-grained model for water, we determine the extent of occupancy of water at protein-protein interfaces and in protein-ligand cavities. The model captures essential findings from all-atom molecular dynamics studies on the same systems by distinguishing protein cavities that dry from those that remain wet. We also interpret the origin of the cavitation inside the melittin tetramer on simple thermodynamic grounds, and show that part of the mellitin surface is sufficiently hydrophobic to trigger cavitation. Using Glauber/Kawasaki dynamics we obtain the time-scales for de-wetting events that are in agreement with those from all-atom simulations. The method can serve as an intermediate step between the necessary initial screening that identifies proteins with abundance of hydrophobic patches using bioinformatics tools (L. Hua, X. H. Huang, P. Liu, R. H. Zhou and B. J. Berne, J. Phys. Chem. B, 2007, 111, 9069), and computationally extensive studies that need to incorporate molecular details (e.g. single mutation studies of amino acid residues).     

Mechanisms Involved in the Modification of Textiles by Non-Equilibrium Plasma Treatment

Plasma methods are often employed for the desired wettability and soaking properties of polymeric textiles, but the exact mechanisms involved in plasma–textile interactions are yet to be discovered. This review presents the fundamentals of plasma penetration into textiles and illustrates mechanisms that lead to the appropriate surface finish of fibers inside the textile. The crucial relations are provided, and the different concepts of low-pressure and atmospheric-pressure discharges useful for the modification of textile’s properties are explained. The atmospheric-pressure plasma sustained in the form of numerous stochastical streamers will penetrate textiles of reasonable porosity, so the reactive species useful for the functionalization of fibers deep inside the textile will be created inside the textile. Low-pressure plasmas sustained at reasonable discharge power will not penetrate into the textile, so the depth of the modified textile is limited by the diffusion of reactive species. Since the charged particles neutralize on the textile surface, the neutral species will functionalize the fibers deep inside the textile when low-pressure plasma is chosen for the treatment of textiles.     

Novel N-chlorinated derivatives of 2H-1-benzopyran-2-imines

A series of new N-chlorobenzopyran-2-imines were prepared in moderate to good yields, by reacting sodium hypochlorite in an acidic medium with benzopyran-2-imines obtained via the Knoevenagel condensation. Some of the N-chlorobenzopyran-2-imines obtained are potential antiproliferating agents.     

Cleaning of Porous Aluminium Titanate by Oxygen Plasma

The removal of organic contaminants from porous Al₂TiO₅ during treatment in oxygen plasma was studied by optical emission spectroscopy (OES). The samples of Al₂TiO₅ were immersed into water emulsion of mineral oil for 3 h to get soaked. Then, they were thoroughly cleaned in ultrasound to remove oil from the surface. Samples were later exposed to RF oxygen plasma at the pressure of 75 Pa. The plasma density was about 2 × 10¹⁶ m⁻³, the electron temperature was about 6 eV and the density of neutral oxygen atoms was about 2 × 10²¹ m⁻³. Optical emission spectra between 200 and 1,000 nm were measured continuously during plasma treatment. The CO peak resulting from oil oxidation reached a well-pronounced maximum between 100 and 150 s of plasma treatment. The maximum in CO corresponded well with a minimum in O peaks. Concentration of oil in the samples was estimated by energy dispersion X-ray analysis. Initially the samples showed high concentration of carbon (about 38 at.%), while after plasma treatment the carbon concentration decreased below the detection limit. The cleaning efficiency was explained by diffusion of oil towards the surface where it was removed by oxidation with oxygen radicals.     

Tunable carbon-carbon and carbon-sulfur cross-coupling of boronic acids with 3,4-dihydropyrimidine-2-thiones

Direct microwave-assisted Pd(0)-catalyzed/Cu(I)-mediated carbon-carbon cross-coupling of 3,4-dihydropyrimidine-2-thiones and boronic acids under Liebeskind-Srogl conditions leads to 2-aryl-1,4-dihydropyrimidines in moderate to high yield. In contrast, Cu(II)-mediated reaction of the same substrates leads to carbon-sulfur cross-coupling. [reaction: see text]     

Use of HPTLC for Quantitative Evaluation of Inulin in Food Products

JPC – Journal of Planar Chromatography – Modern TLC - HPTLC and HPLC—MS methods have been developed for quantitative determination of inulin in food products. Samples were applied...     

QASKI – the quality assurance system of the National Institute of Chemistry

 The quality assurance system (QASKI) developed and implemented in the National Institute of Chemistry is presented. It tries to eliminate the incompatibilies between the present methods of quality assurance used in research and development institutes such as good laboratory practice and accreditation. Since 1991, QASKI has been used for internal accreditation of laboratories located in the institute, regardless of the fact that some of them deal with routine analyses and others with research and development. Every laboratory that wishes to ensure the credibility of its research or routine work enters QASKI and at the same time chooses an external method of approval. All interested laboratories, study directors, principal investigators, internal auditing staff, heads of documentation, quality assurance unit staff, the Director of the institute and the Quality Management Board participate in the internal system.     

Synthesis and functionalization oftrans-2-(2′-aminocyclohexyloxy)-andtrans-2-(2′-azidocyclohexyloxy)acetic acid

Summary Synthesis of the hydrochloride oftrans-2-(2-aminocyclohexyloxy)acetic acid (4) fromtrans-2-(2-azidocyclohexyloxy)acetic acid (1) is described.4 was acylated at the amino group to give compounds5–8.1 was converted into acid chloride (9) and amides10–13.

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Synthese und Funktionalisierung dertrans-2-(2-Aminocyclohexyloxy)- undtrans-2-(2-Azidocyclohexyloxy)essigsäure

Zusammenfassung Die Synthese destrans-2-(2-Aminocyclohexyloxy)essigsäurehydrochlorids (4), ausgehend vontrans-2-(2-Azidocyclohexyloxy)essigsäure (1), wird beschrieben.4 wurde durch Acylierung der Aminogruppe in die Verbindungen5–8 übergeführt.1 wurde in das Säurechlorid9 und die Carbonsäureamide10–13 umgewandelt.

     

Membrane switch hypothesis. 2. Domain structure of phagocytes in horses with recurrent airway obstruction

The mechanism of recurrent airway obstruction (RAO) in horses was investigated by measuring the membrane domain structure and oxy-redoxy activity in phagocytes isolated from bronchoalveolar lavage fluid (BAL) and from the blood of healthy and RAO horses by electron paramagnetic resonance (EPR). Differences in the activity of intracellular antioxidant enzymes CAT, GPx, and SOD measured in phagocytes of RAO horses in comparison to healthy horses showed that the phagocytes were affected by oxidative stress. In comparison with polymorphonuclear leukocytes (phagocytes) from the blood of healthy horses the reduction mechanisms in BAL were faster and coincided with the merging of disordered membrane domains, while in horses with RAO the reduction and membrane domain structure remained unchanged. We assume that the merging of lipid domains observed in phagocytes from BAL of healthy horses could promote cluster formation of membrane proteins or ligands, which could trigger the activation process in phagocytes of healthy horses and consequently the physiological response that probably did not happen in phagocytes of RAO horses.