SERS and Raman imaging as a new tool to monitor dyeing on textile fibres

Textile fibres containing Ag nanoparticles have been widely explored for a number of antimicrobial fabrics. Moreover, it is well‐known that textile dyeing is a critical stage in the manufacture thereof. This research shows that surface enhanced Raman scattering (SERS) and Raman imaging can be used with advantage in the monitoring of this process. Using Ag containing linen fibres stained with methylene blue (MB), it was possible to map the local distribution of the MB dye in the fibres by Raman imaging. MB was selected as the SERS molecular probe and as a model dye. Composites of linen fibres and Ag nanoparticles were prepared by distinct methods and used as SERS substrates in order to evaluate the effect of the preparative method on the Raman images. Our results demonstrate that by using Raman imaging associated to the presence of Ag nanoparticles, it is possible to distinguish the local distribution of the dye on the textile surface. This investigation allows to foreseeing the use of this technique in terms of quality control of Ag containing fabrics, which is a market in great expansion. Copyright © 2016 John Wiley & Sons, Ltd.     

Sensitivity-Enhanced 13C-NMR Spectroscopy for Monitoring Multisite Phosphorylation at Physiological Temperature and pH

Abundant phosphorylation events control the activity of nuclear proteins involved in gene regulation and DNA repair. These occur mostly on disordered regions of proteins, which often contain multiple phosphosites. Comprehensive and quantitative monitoring of phosphorylation reactions is theoretically achievable at a residue-specific level using ¹H-¹⁵N NMR spectroscopy, but is often limited by low signal-to-noise at pH>7 and T>293 K. We have developed an improved ¹³Cα-¹³CO correlation NMR experiment that works equally at any pH or temperature, that is, also under conditions at which kinases are active. This allows us to obtain atomic-resolution information in physiological conditions down to 25 μm . We demonstrate the potential of this approach by monitoring phosphorylation reactions, in the presence of purified kinases or in cell extracts, on a range of previously problematic targets, namely Mdm2, BRCA2, and Oct4.     

Homogeneous isotope exchange between tungsten(VI) and Keggin and Dawson type uranium polyoxotungstophosphates

The present paper is concerned with the isotope exchange between¹⁸⁵W and tungsten, and³²P and phosphorus respectively, in uranium(IV) trivacant Keggin and Dawson polyoxotungstophosphate complexes, in water. These studies were carried out at different concentrations and temperature. The isotope exchange rate increases with the temperature and the reagents' concentration. The experimental results show that the complexes are labile kinetically.     

Hydrolytically stable arabinofuranoside analogs for the synthesis of arabinosyltransferase inhibitors

The first members of two new families of arabinosyltransferase inhibitors, derived from previously reported hybrid compounds covalently associating an iminoalditol with an α-d-arabinofuranoside, have been prepared. In place of the arabinofuranoside moiety, they incorporate in their structure a suitably substituted tetrahydrofuran (C-glycoside family) or a cyclopentane (carba-sugar family) for mimicking the α-d-arabinofuranoside ring.     

Process Parameters Optimization,Characterization, and Application of KOH-Activated Norway Spruce Bark Graphitic Biochars for Efficient Azo Dye Adsorption

In this work, Norway spruce bark was used as a precursor to prepare activated biochars (BCs) via chemical activation with potassium hydroxide (KOH) as a chemical activator. A Box–Behnken design (BBD) was conducted to evaluate and identify the optimal conditions to reach high specific surface area and high mass yield of BC samples. The studied BC preparation parameters and their levels were as follows: pyrolysis temperature (700, 800, and 900 °C), holding time (1, 2, and 3 h), and ratio of the biomass: chemical activator of 1: 1, 1.5, and 2. The planned BBD yielded BC with extremely high SSA values, up to 2209 m²·g⁻¹. In addition, the BCs were physiochemically characterized, and the results indicated that the BCs exhibited disordered carbon structures and presented a high quantity of O-bearing functional groups on their surfaces, which might improve their adsorption performance towards organic pollutant removal. The BC with the highest SSA value was then employed as an adsorbent to remove Evans blue dye (EB) and colorful effluents. The kinetic study followed a general-order (GO) model, as the most suitable model to describe the experimental data, while the Redlich–Peterson model fitted the equilibrium data better. The EB adsorption capacity was 396.1 mg·g⁻¹. The employment of the BC in the treatment of synthetic effluents, with several dyes and other organic and inorganic compounds, returned a high percentage of removal degree up to 87.7%. Desorption and cyclability tests showed that the biochar can be efficiently regenerated, maintaining an adsorption capacity of 75% after 4 adsorption–desorption cycles. The results of this work pointed out that Norway spruce bark indeed is a promising precursor for producing biochars with very promising properties.     

Ion‐exchange resins. III. Functionalization–morphology correlations in the synthesis of some macroporous,strong basic anion exchangers and uranium‐sorption properties evaluation

The synthesis and characterization of a series of macroporous, strong basic anion exchangers (SBAEs), with an average pore radius higher than 50 nm, and the evaluation of their sorption properties for uranyl chlorocomplexes from HCl solutions are reported. Finely divided macroporous styrene–divinylbenzene (S–DVB) copolymers with a narrow distribution of beads sizes, diameters within the range of 90–200 μm, were prepared for this purpose with 2‐ethyl‐1‐hexanol as a porogen, at a high dilution of monomers (D ≥ 0.55 mL/mL). Chloromethyl groups were introduced with (CH₂O)_n/Me₃SiCl as a chloromethylation agent in the presence of a Lewis acid as a catalyst (TiCl₄, SnCl₄, and FeCl₃) in CHCl₃ as a reaction medium. SnCl₄ and FeCl₃ gave comparable chloromethylation degrees in the same reaction conditions. TiCl₄ was not efficient as a catalyst in the chloromethylation with this reagent. Diethyl‐2‐hydroxyethylamine was used as a tertiary amine to prepare SBAEs. Structural and morphological characteristics were determined after every functionalization step of the macroporous network. Both the chloromethylation, in the presence of FeCl₃ as a catalyst, and the amination reactions determined a significant decrease of the pore volume, in the whole range of the nominal crosslinking degree, comparative with the starting copolymer. The specific surface area and the average pore radius varied in a different way as a function of the nominal crosslinking degree. Thus, the specific surface area increased and the average pore radius decreased after chloromethylation and amination for copolymers with a DVB content lower than 10 wt %. Small decreases of the specific surface area and the average pore radius were observed after chloromethylation and amination reactions for copolymers with a DVB content higher than 10 wt %. SBAEs were also characterized by thermogravimetric analysis and sorption capacity for uranyl chlorocomplexes. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2451–2461, 2004     

Generic tropical initial ideals of Cohen-Macaulay algebras

We study the generic tropical initial ideals of a positively graded Cohen-Macaulay algebra R over an algebraically closed field k. Building on work of Römer and Schmitz, we give a formula for each initial ideal, and we express the associated quasivaluations in terms of certain I-adic filtrations. As a corollary, we show that in the case that R is a domain, every initial ideal coming from the codimension 1 skeleton of the tropical variety is prime, so “generic presentations of Cohen-Macaulay domains are well-poised in codimension 1.”