Effect of heterocyclic ring system on formation of dimeric quinolones under catalyst-free conditions: a green approach

The intermediate-dependent green and efficient synthesis of dimeric quinolones 4a–l and 7a–l by the Knoevenagel condensation followed by Michael-type addition of 4-hydroxy-1-methylquinolin-2(1H)-one 1a, b to indole-3-aldehydes 2a–f and aromatic aldehydes 5a–l in water through the condensed compound 3a–l under catalyst-free conditions is described. This reaction was found to be environmentally friendly, has easy-workup and shorter reaction times giving good yields of the product without the need for its isolation using column chromatography.     

Mechanically-induced dimensional extensibility of fibers towards tough fiber networks

The beneficial effect of materials with high aspect ratio as composite reinforcement has prompted continuous interest towards cellulosic fibers. Besides providing stiffness, fibers can potentially contribute to composite extensibility. While mechanical treatments are typically used to adjust the physical and surface properties of fibers, less is known about ensuing effects on their extensibility and that of associated networks. Fiber network dimensional extensibility of 16% was achieved by processing the precursor aqueous fiber dispersions following a simple mechanical treatment with a judicious combination of low (PFI refining) and high concentrations and temperatures (Wing defibrator). Consequently, deformation of fibers and increased inter-fiber bonding resulted in a three-fold increase in strength to rupture of the fiber network leading to the structures with unprecedented toughness.     

Analysis of moisture sorption in lyocell-polypropylene composites

The preparation of composites by thermoforming of intermingled fibre slivers is an efficient method to receive high performance and lightweight materials. Cellulosic fibres have benefits like low density and sustainability but the sorption of water due to the high hydrophilicity of the cellulose requires attention. The swelling of the wet fibres changes the fibre-matrix adhesion and as a consequence, the mechanical strength of the composite is influenced negatively. In this study, the thermoplastic polypropylene was combined with lyocell fibres as reinforcement. Moisture sorption isotherms of cellulose/polypropylene composites were recorded as function of relative humidity. Additionally, the specific surface area was analysed by the Brunauer–Emmett–Teller model. It has been found, that the moisture sorption is influenced by the polypropylene (PP) ratio in the composites. At 60% relative humidity the moisture uptake of the lyocell fibres was reduced from 10.8 to 5.8% for lyocell embedded in a composite with 50% polypropylene. Besides the hysteresis between moisture sorption/desorption cycles was found to be proportional to the increased content of PP. The “Parallel Exponential Kinetics” (PEK) model was used to analyse the kinetics of moisture sorption of these composites in more detail. With the help of the PEK model the sorption/desorption kinetics were described by a fast and slow moisture sorption/desorption process. The capacity for rapid moisture sorption is reduced by the formation of PP layers on the lyocell surface. The share of slow moisture sorption increased with increasing PP content in the composite. The results support understanding of the interaction of water with cellulose containing composites.     

Physical properties and thermal behavior of reconstituted tobacco sheet with precipitated calcium carbonate added in the coating process

Addition of precipitated calcium carbonate (PCC) to cellulosic products can reduce production costs and modify their physical properties. This study investigated the effects of adding PCC on the properties of reconstituted tobacco sheet (RTS), a cellulosic product. Scanning electron microscopy (SEM) analysis showed that adding PCC to the coating could modify the surface microstructure of RTS. With increasing PCC addition, the strength and tar release per cigarette of RTS decreased. However, the filling capacity, bulk, and CO release content in the mainstream smoke reached optimal values when the proportion of PCC in the coating was 8%. Thermogravimetry (TG) and differential thermogravimetry (DTG) analysis indicated that the main thermal pyrolysis stage occurred in the range of 200–400 °C, similar to cellulosic components. The Coats–Redfern equation was used to analyze the thermal pyrolysis mechanism. The fitting results showed that, in the range of 200–280 °C, the best fit model for RTS with 4 or 8% PCC was diffusion-controlled reaction (D1) with fitting correlation coefficient (r ²) of 0.9630 and 0.9576, respectively. Meanwhile, in the range of 280–400 °C, the most reliable fitting model for RTS with 4% PCC was chemical reaction (F2) with r ² = 0.9681. One reaction model could not describe the thermal pyrolysis of RTS with 12% PCC in the main decomposition stage. The thermal kinetic parameters suggested that addition of PCC to RTS coatings could modify the thermal pyrolysis mechanism, but did not change the peak temperatures in the main thermal decomposition stage. This study demonstrates that addition of PCC to RTS coating is a promising method to improve its quality.     

Ag@AgCl embedded on cellulose film: a stable,highly efficient and easily recyclable photocatalyst

In this work, cellulose–Ag@AgCl composite films have been fabricated directly through a one-step coagulation of a cellulose/1-butyl-3-methylimidazolium chloride (BmimCl) solution with AgNO₃ and PVP. The AgCl was formed upon the addition of AgNO₃ to a cellulose/BmimCl solution, and underwent further reaction with excess Cl^?, leading to the complete dissolution of AgCl. The AgCl crystals were regenerated on the cellulose matrix during the coagulation process. The AgCl was partial decomposed to Ag⁰ and formed Ag@AgCl under visible light irradiation. The morphology of Ag@AgCl in the cellulose matrix was controlled by varying the concentration of PVP. The addition of PVP enabled the formation of stable cellulose films embedded with Ag@AgCl. The composite film demonstrated efficient photodegradation of methyl orange, which was retained upon recycling. This work thus provides a simple pathway for the preparation of Ag@AgCl embedded on a polymer support via one-step coagulation.     

Preparation of phthalocyanine-bound myristoyl celluloses for photocurrent generation system

The influences of two structural modifications on the photocurrent generation performance of the Langmuir–Blodgett (LB) film of the 6-O-phthalocyaninyl cellulose derivative were investigated. These structural modifications were the substituent groups at the O-2 and O-3 positions, and the central metal of the phthalocyanine moiety. Specifically, 6-O-Zn/phthalocyaninyl- (8a) and Pd/phthalocyaninyl (8b) -2,3-di-O-myristoylcelluloses were prepared instead of 6-O-Zn/phthalocyaninyl-2,3-di-O-myristylcellulose (2). The LB monolayer film of compound 8a on an indium thin oxide electrode showed higher photocurrent generation performance than that of compound 2. This suggested that myristoyl groups (C-14 acyl groups) were more beneficial to photocurrent generation than myristyl groups (C-14 alkyl groups), as the substituent at the O-2 and O-3 positions. The LB monolayer film of compound 8b showed photocurrent generation from 500 to 700 nm, although a blue-shift in the Q-band maximum was observed. The photocurrent generation performance of compound 8b was significantly higher than that of compound 8a. This indicated that Pd was more beneficial to photocurrent generation than Zn. The film of compound 8b prepared by the horizontal lifting method showed better photocurrent generation performance than that prepared by the vertical dipping method. Consequently, compound 8b is a complementary material to the porphyrin-appended cellulose derivative (1) for photocurrent generation system.     

On the syzygies and Hodge theory of nodal hypersurfaces

We give lower bounds for the degree of the syzygies involving the partial derivatives of a homogeneous polynomial defining an even dimensional nodal hypersurface. This implies the validity of formulas due to M. Saito, L. Wotzlaw and the author for the graded pieces with respect to the Hodge filtration of the top cohomology of the hypersurface complement in many new cases. A classical result by Severi on the position of the singularities of a nodal surface in \(\mathbb {P}^3\) is improved and applications to deformation theory of nodal surfaces are given.     

On the power of rewinding simulators in functional encryption

In a seminal work, Boneh, Sahai and Waters (BSW) [TCC’11] showed that for functional encryption the indistinguishability notion of security (IND-Security) is weaker than simulation-based security (SIM-Security), and that SIM-Security is in general impossible to achieve. This has opened up the door to a plethora of papers showing feasibility and new impossibility results. Nevertheless, the quest for better definitions that (1) overcome the limitations of IND-Security and (2) the known impossibility results, is still open. In this work, we explore the benefits and the limits of using efficient rewinding black-box simulators to argue security. To do so, we introduce a new simulation-based security definition, that we call rewinding simulation-based security (RSIM-Security), that is weaker than the previous ones but it is still sufficiently strong to not meet pathological schemes as it is the case for IND-Security (that is implied by the RSIM). This is achieved by retaining a strong simulation-based flavour but adding more rewinding power to the simulator having care to guarantee that it can not learn more than what the adversary would learn in any run of the experiment. What we found is that for RSIM  the BSW impossibility result does not hold and that IND-Security is equivalent to RSIM-Security for attribute-based encryption in the standard model. Nevertheless, we prove that there is a setting where rewinding simulators are of no help. The adversary can put in place a strategy that forces the simulator to rewind continuously.     

Distributional Transformations Without Orthogonality Relations

Distributional transformations characterized by equations relating expectations of test functions weighted by a given biasing function on the original distribution to expectations of the test function’s higher derivatives with respect to the transformed distribution play a great role in Stein’s method and were, in great generality, first considered by Goldstein and Reinert (J Theoret Probab 18(1):237–260, 2005. doi: 10.1007/s10959-004-2602-6). We prove two abstract existence and uniqueness results for such distributional transformations, generalizing their \(X-P\)-bias transformation. On the one hand, we show how one can abandon previously necessary orthogonality relations by subtracting an explicitly known polynomial depending on the test function from the test function itself. On the other hand, we prove that for a given nonnegative integer m, it is possible to obtain the expectation of the m-th derivative of the test function with respect to the transformed distribution in the defining equation, even though the biasing function may have \(k<m\) sign changes, if these two numbers have the same parity. We explain how these results can be used to guarantee the existence of two different generalizations of the zero-bias transformation by Goldstein and Reinert (Ann Appl Probab 7(4):935–952, 1997. doi: 10.1214/aoap/1043862419). Further applications include the derivation of Stein-type characterizations without needing to solve any Stein equation and the presentation of a general framework for estimating the distance from the distribution of a given real random variable X to that of a random variable Z, whose distribution is characterized by some mth-order linear differential operator. We also explain the fact that, in general, the biased distribution depends on the choice of the sign change points, if these are ambiguous. This new phenomenon does not appear in the framework from Goldstein and Reinert (2005).     

The Matsumoto–Yor Property and Its Converse on Symmetric Cones

The Matsumoto–Yor (MY) property of the generalized inverse Gaussian and gamma distributions has many generalizations. As was observed in Letac and Weso?owski (Ann Probab 28:1371–1383, 2000), the natural framework for the multivariate MY property is symmetric cones; however, they prove their results for the cone of symmetric positive definite real matrices only. In this paper, we prove the converse to the symmetric cone-variate MY property, which extends some earlier results. The smoothness assumption for the densities of respective variables is reduced to continuity only. This enhancement was possible due to the new solution of a related functional equation for real functions defined on symmetric cones.