Alternating Copolymers of Cyclopenta[2,1‐b;3,4‐b′]dithiophene and Thieno[3,4‐c]pyrrole‐4,6‐dione for High‐Performance Polymer Solar Cells

A series of alternating copolymers of cyclopenta[2,1‐b;3,4‐b′]dithiophene (CPDT) and thieno[3,4‐c]pyrrole‐4,6‐dione (TPD) have been prepared and characterized for polymer solar cell (PSC) applications. Different alkyl side chains, including butyl (Bu), hexyl (He), octyl (Oc), and 2‐ethylhexyl (EH), are introduced to the TPD unit in order to adjust the packing of the polymer chain in the solid state, while the hexyl side chain on the CPDT unit remains unchanged to simplify discussion. The polymers in this series have a simple main chain structure and can be synthesized easily, have a narrow band gap and a broad light absorption. The different alkyl chains on the TPD unit not only significantly influence the solubility and chain packing, but also fine tune the energy levels of the polymers. The polymers with Oc or EH group have lower HOMO (highest occupied molecular orbital) and LUMO (lowest unoccupied molecular orbital) energy levels, resulting higher open circuit voltages (V_oc) of the PSC devices. Power conversion efficiencies (PCEs) up to 5.5% and 6.4% are obtained from the devices of the Oc substituted polymer (PCPDTTPD‐Oc) with PC₆₁BM and PC₇₁BM, respectively. This side chain effect on the PSC performance is related to the formation of a fine bulk heterojunction structure of polymer and PCBM domains, as observed with atomic force microscopy.     

Promising antifungal effect of some Euro-Asiatic plants against dangerous pathogenic and toxinogenic fungi

BACKGROUND: Increasing evidence of fungicide‐resistant toxinogenic and pathogenic fungal species is obvious. Looking for new possibilities of antifungal treatment or sources of antifungal substances is a major problem. Some medicinal plants exert strong antifungal properties and could be conveniently used as a promising alternative source for presently problematic antifungal treatment in many areas with respect to their natural origin. Methanol extracts of 46 medicinal plants from the Eurasian area were used in a screening assay for antifungal activity in this study. The growth inhibitory effect was tested against six significant pathogenic and toxinogenic fungal species: Fusarium oxysporum, F. verticillioides, Penicillium expansum, P. brevicompactum, Aspergillus flavus and A. fumigatus. RESULTS: For 14 plant species, the possibility of using them as natural fungicides was indicated. The extract from Grindelia camporum showed significant activity against all target fungal species. The most sensitive target fungus was the toxinogenic and human pathogenic species A. fumigatus. CONCLUSION: This study has identified 14 extracts of medicinal plants with a potential use as an antifungal treatment in various areas. One of them showed promising efficiency against all selected significant pathogenic and toxinogenic fungal species. Copyright © 2010 Society of Chemical Industry     

PBT blends with rigid polymer and elastomer inclusions: the effect of component type and reactivity on mechanical behaviour

The present study shows the potential of the poly(butylene terephthalate) (PBT) matrix to form ternary blends with well‐balanced properties, analogous to Polyamide 6 (PA6) systems with a very fine (<100 nm) separately dispersed rigid polymer (poly(styrene‐co‐maleic anhydride)) and elastomer (maleated ethylene‐propylene elastomer). The use in PBT blends of maleated components analogous to those in the PA6 systems was much less effective, due to the presence of larger particles. Enhancement of all properties, including toughness, was found in the case of a blend containing at least one component with epoxide groups, such as rigid styrene‐glycidyl methacrylate copolymer or elastomeric poly[(ethylene)‐co‐(methyl acrylate)‐co‐(glycidyl methacrylate)]. In this case, the reactive compatibilization of the epoxy‐group‐containing component caused refinement of particle size of the other component due to enhanced viscosity. As a result, more advantageous micromechanical behaviour of this ternary in comparison with the binary system occurs. The PBT matrix offers a similar potential to PA6 in synergistic influencing of both well‐dispersed phases. This work supports the universality of rigid polymer‐elastomer combination for the enhancement of the properties of pseudoductile polymers. Copyright © 2004 Society of Chemical Industry     

Monoclonal antibody R5 for detection of putatively coeliac-toxic gliadin peptides

Monoclonal antibody R5 against rye secalin was recently suggested to be useful in analysis of gluten in food. The epitope specificity of R5 was characterized and compared with those of eight other monoclonal antibodies (mabs) against gliadins (gli) and secalins. Mabs were tested for binding to synthetic peptides spanning in overlapping manner sequences of gli. In a luminescence assay R5 bound to all peptides from the N-terminal part of α-type gli hitherto known to induce in sensitive patients with coeliac disease after in vivo instillation. Thus, R5 proves to be very useful for gluten analysis. Sequences QQPFP, QQQFP, LQPFP, and QLPFP were bound most strongly. Substitution of glutamine by glutamic acid in the epitope may decrease binding of R5 dependent on surrounding amino acids. One of the positions of the substitutions diminishing antibody binding was a typical site of attack of tissue transglutaminase, the enzyme converting by deamidation cereal prolamins into their disease active form. Investigation of eight other mabs against gli and secalins showed binding properties very similar to R5. We speculate the sequence QQQ/PFP seems to represent an immunodominant structure in prolamins. An erratum to this article can be found at     

Bestimmung der Zerst?rung von Trypsininhibitoren w?hrend der Sojabohnenentbitterung

Zusammenfassung Die Untersuchung der Proteolyse durch Trypsin bei unterschiedlichen Konzentrationen von Sojaextrakten ermöglicht eine genauere Bestimmung der Antitrypsin Aktivität als die üblichen Methoden. Im Laufe der Entbitterung durch Wasserdampf werden Trypsininhibitoren fast völlig inaktiviert; beim trockenen Erhitzen ist jedoch die Inaktivierung sehr langsam. Zwischen den Resultaten der Bestimmung der Antitrypsin-und der Uresse-Aktivität ist die Korrelation gut, wenn die Inaktivierung in nassem Millieu verläuft, in trockenem Material wird die Urease beim Erhitzen wesentlich schneller als die Trypsininhibitoren inaktiviert.     

A mechanistic study of methyl parathion hydrolysis by a bifunctional organoclay

The mechanism for the hydrolysis of methyl parathion (MP) by a bifunctional quaternary-ammonium based long-chained organclay(LCOC) containing an alkylamine (-CH2CH2-NH2) headgroup was elucidated. The pathway of the catalytic hydrolysis of methyl parathion by the LCOC was defined by following the effect of replacing H20 with D20, by replacing the primary amino headgroup by a tertiary amino group, and by a detailed mathematical analysis of the proposed reaction scheme. A phosphorothioate isomer of MP was formed in the presence of the LCOC as an intermediate reaction product, initially increasing in concentration and then disappearing. The isotope effect was minimal and substituting a tertiary amine in the LCOC increased the rate of MP hydrolysis. A mechanism is proposed in which hydrolysis of MP can proceed via both a direct route (specific base hydrolysis) and through the formation of the isomer which then undergoes specific base hydrolysis more rapidly than the parent MP. The relative importance of each pathway is a function of pH with the direct hydrolysis of MP being predominant at higher pH values (pH > 10) and the isomer intermediate pathway predominating at lower pH values (pH approximately 8-10).     

Persistent organic pollutants in ringed seals from the Russian Arctic

Organochlorine compounds total DDT (ΣDDT), total HCH isomers (ΣHCH), toxaphenes (sum of Parlar 26, 50, 62), mirex, endrin, methoxychlor, total chlorinated benzenes (ΣCBz), total chlordane compounds (ΣCHL), polychlorinated biphenyls (total of 56 congeners; ΣPCBs), polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs), and polybrominated diphenyl ethers (sum of 7 tri- to hepta congeners; ΣPBDEs) were analysed in the blubber of adult ringed seals from the four areas of the Russian Arctic (White Sea, Barents Sea, Kara Sea and Chukchi Sea) collected in 2001-2005. Ringed seals from the south-western part of the Kara Sea (Dikson Island — Yenisei estuary) were the most contaminated with ΣDDTs, ΣPCBs, ΣCHL, and mirex as compared with those found in the other three areas of Russian Arctic, while the highest mean concentrations of ΣHCHs and PCDD/Fs were found in the blubber of ringed seals from the Chukchi Sea and the White Sea, respectively. Among all organochlorine compounds measured in ringed seals from the European part of the Russian Arctic, concentrations of ΣDDT and ΣPCBs only were higher as compared with the other Arctic regions. Levels of all other organochlorine compounds were similar or lower than in seals from Svalbard, Alaska, the Canadian Arctic and Greenland. ΣPBDEs were found in all ringed seal samples analysed. There were no significant differences between ΣPBDE concentrations found in the blubber of ringed seals from the three studied areas of the European part of the Russian Arctic, while PBDE contamination level in ringed seals from the Chukchi Sea was 30-50 times lower. ΣPBDE levels in the blubber of seals from the European part of the Russian Arctic are slightly higher than in ringed seals from the Canadian Arctic, Alaska, and western Greenland but lower compared to ringed seals from Svalbard and eastern Greenland.     

Objective evaluation of multidirectional fabric creasing

Creasing is one of the most important properties of textiles for apparel application. Most fabrics are regularly evaluated by means of etalons, that is, visual standards. Nevertheless, due to the disadvantages of visual evaluation, which is unreliable and time consuming, several objective methods were developed. In this article, a new objective method of multidirectional evaluation of creasing is described. We have proposed the test method of angle recovery using image processing. The specimen of the fabric was of a circular shape and it was measured by the method of angle recovery in various directions. We compared the results obtained from our method with the method described by Sommer and by the hollow cylinder method also. We found good conformity between the results obtained from our method and the method described by Sommer.     

Study of the compositional heterogeneity of ethylene/1–hexene copolymers produced over supported catalysts of different composition

Separation into narrow MWD fractions (liquid–liquid fractionation) and preparative TREF (temperature rising elution fractionation) with subsequent analysis of fractions by GPC, FTIR, and ¹³C NMR spectroscopy were used to study the comonomer distribution of ethylene/1–hexene copolymers produced over highly active supported titanium‐ and vanadium‐magnesium catalysts (TMC and VMC) and a supported zirconocene catalyst. These catalysts produce PE with different MWD: M_w/M_n values vary from 2.9 for zirconocene catalyst, 4.0 for TMC, and 15 for VMC. 1‐Hexene increases polydispersity to 25 for copolymer produced over VMC and hardly affects MWD of the copolymer produced over TMC and zirconocene catalysts. The most broad short chain branching distribution (SCBD) was found for ethylene/1–hexene copolymers produced over TMC. VMC and supported zirconocene catalyst produce copolymers with uniform profile of SCB content vs. molecular weight in spite of great differences in M_w/M_n values (22 and 2.5 respectively). TREF data showed that majority of copolymer produced over supported zirconocene catalyst was eluted at 70–90°C (about 85 wt %). In the case of VMC copolymer's fractions were eluted in the broad temperature interval (40–100°C). Accordingly, TREF data indicate a more homogeneous SCBD in copolymer, produced over supported zirconocene catalyst. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012