Synthesis and testing of cellulose acetate nicotinate as adsorbent for rhodamine B dye

The esterification of cellulose hydroxyl groups with natural carboxylic acids in mild conditions represents an adequate pathway in obtaining cellulose derivatives with different useful properties. In this article, authors report the synthesis of new mixed ester of cellulose and cellulose acetate nicotinate (CAN) , in a homogenous medium using DMF as solvent, cellulose acetate (CA) as starting cellulosic material, and nicotinic acid as an esterification agent in the presence of p-toluenesulfonyl chloride and pyridine. FTIR and NMR techniques were used to prove the binding of nicotinoyl group at free hydroxyl groups of CA. The obtained CAN was electrospun by electrospinning technique to obtain adsorbent ultrafine fibers, evidenced by SEM images, with high specific surface area. Monolayer Langmuir and empirical Leundrich isotherms were used to assess the adsorption capacity for rhodamine B dye of electrospun CAN in comparison with that of electrospun CA used as starting material. Langmuir isotherm led to a better assessment of experimental data suggesting that the adsorption is mainly determined by hydrogen bonds formed between carboxylic OH hydrogen bonding donor and pyridine N hydrogen bonding acceptor. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47772.     

Co/SiO2 catalysts prepared from Co2(CO)8 for CO hydrogenation into alcohols and hydrocarbons: characterization by magnetic methods and temperature-programmed hydrogenation

The hydrogenation of carbon monoxide over Co/SiO₂ catalysts obtained by reduction of precursors prepared by the reaction of dicobaltoctacarbonyl with silica gives rise to a mixture of alcohols and hydrocarbons. The chain growth probability for hydrocarbon synthesis is similar to that observed over conventional catalysts prepared by the ammonia method (=0.74) with a comparable metal dispersion (metal particle size 4 nm). Alcohol formation yields a smaller chain growth probability (=0.42). Magnetic measurements have shown that in the latter catalyst, small cobalt clusters (1 nm) are likely to be present together with the cobalt particles (4 nm), this observation reconciles apparently conflicting results from the literature. It has been speculated that alcohol formation might be related to the presence of these clusters according to a concerted mechanism. Furthermore, the observation of large amounts of acetates by temperature-programmed hydrogenation, not detected in hydrocarbon selective catalysts, suggests that they may play a role in ethanol synthesis.     

DSP-based bottleneck bandwidth estimation

This paper presents a new passive technique for estimating the bottleneck bandwidth based on transferring the Gaussian kernel density estimation of the packets inter-arrival times to the frequency domain. The resulting spectrum contains information about the transmission time of the bottleneck link and can reveal information about multiple bottlenecks if they exist along the end-to-end path. The advantage of the technique is that it provides a model that can be manipulated by the digital signal processing methods and, unlike prior work in the area, it relies less on statistical methods. The proposed technique was validated using the ns2 network simulator [1] on several topologies and traffic sources. Further experiments were conducted to test the strength of the patterns between flows that share a bottleneck by applying K-means algorithm to cluster the average packet inter-arrival times of these flows. The paper also presents a set of results from real traffic experiments conducted in order to infer both the bottleneck bandwidth and the capacity of the path using a passive approach.     

Interactions between Polymeric Dispersants and Calcium Silicate Hydrates

To better understand the mechanism of interaction between hydrating silicate-based cements and polymeric dispersants of the type used as "superplasticizers" in modern construction concretes, two different types of polymeric dispersant were added (at concentrations of 1 and 10 g/L) during the synthesis of calcium silicate hydrate (C-S-H) via the "pozzolanic reaction" in dilute slurries of lime and reactive silica, at Ca/Si ratios in the range of 0.66–1.50. Although both polymers gave degrees of adsorption of >79% in all cases studied, no significant structural modifications of the resulting C-S-H products were observed via X-ray diffraction or ²⁹Si magic angle spinning–nuclear magnetic resonance. These results differ from recent work in which it was shown that similar types of polymer could intercalate into the interlayers of C-S-H that was made using an alternative process. It is suggested that the process by which the C-S-H is formed may have a strong influence on whether C-S-H can intercalate polymers. This observation is relevant to understanding the fate of such polymers in concrete.     

A study into first and second order thermal transitions of materials using Spectral-DSC

Thermal and spectral analysis is conducted routinely to characterise a large range of materials and compounds. However, tests are often conducted independently on separate samples where comparison between essentially the same material can provide conflicting results. Simultaneous thermal and spectral measurements have the advantage of being able to directly compare results using the same sample. A novel design of a simultaneous thermal and spectral technique is described along with application examples that highlight the benefits of this technique. The thermal analysis was conducted using Differential Scanning Calorimetry (DSC) and the in situ spectral analysis was conducted using a Fourier Transform Near Infrared (FT-NIR) spectrometer. Two examples are used to illustrate the versatility and potential advantages of the combined thermal and spectral method. Analysis of the first and second order transitions of polyethylene terephthalate (PET) is presented along with the pharmaceutical polymorphic conversion of carbamazepine from Form III to Form I through an isothermal hold at 160 °C.     

Calcium Silicate Hydrates Studied by Small-Angle Neutron Scattering (SANS)

Small-angle neutron scattering (SANS) was used to study calcium silicate hydrate (C-S-H) formed via pozzolanic reaction between calcium oxide and ultrafine silica in water or polymer solutions at a temperature of 20°C. The SANS profile of this product was consistent with a structure that consisted of platelets with maximum diameters of ∼20 nm (± 5 nm) in the x – y plane, which was similar to a structure that had been deduced in previous work via X-ray diffractometry. The presence of two different types of superplasticizer in solution (at a concentration of 10 g/L) had no significant effect on its formation kinetics or its SANS profile.     

Spatiotemporal investigations of DNA damage repair using microbeams

Cellular response to radiation damage is made by a complex network of pathways and feedback loops whose spatiotemporal organisation is still unclear despite its decisive role in determining the fate of the damaged cell. Revealing the dynamic sequence of the repair proteins is therefore critical in understanding how the DNA repair mechanisms work. There are also still open questions regarding the possible movement of damaged chromatin domains and its role as trigger for lesion recognition and signalling in the DNA repair context. The single-cell approach and the high spatial resolution offered by microbeams provide the perfect tool to study and quantify the dynamic processes associated with the induction and repair of DNA damage. We have followed the development of radiation-induced foci for three DNA damage markers (i.e. γ-H2AX, 53BP1 and hSSB1) using normal fibroblasts (AG01522), human breast adenocarcinoma cells (MCF7) and human fibrosarcoma cells (HT1080) stably transfected with yellow fluorescent protein fusion proteins following irradiation with the QUB X-ray microbeam (carbon X-rays <2 μm spot). The size and intensity of the foci has been analysed as a function of dose and time post-irradiation to investigate the dynamics of the above-mentioned DNA repair processes and monitor the remodelling of chromatin structure that the cell undergoes to deal with DNA damage.     

Effects of river regulation on the lower Ebro river (NE Spain)

The regulation of the Ebro River in the 1960s has changed the discharge pattern: spring floods have been reduced and, as the reservoirs are used for hydroelectrical purposes, discharge varies daily. The last 50 km of the river have been studied for two years (1986 and 1987). Our main purpose was to establish the particulate organic and inorganic transport of the river and its seasonal changes. Particulate material was sampled in surface and deep waters. Water conductivity ranges between 0.9 and 53 mS, and anoxia is common in summer situations. Particulate C ranges between 1 and 3 mg l^?1 with higher values in summer; particulate N is very similar along the year with values between 0.1 and 0.5 mg l^?1. Effects of regulation seem to be important in supplying very high nutrient content to algae and producing a high biomass and production in the lower part of the river, especially in summer. Diatoms and Chlorophyta are the most abundant groups. Phosphorus is higher than 5 μmol l^?1, with lower values in summer. Most of particulate material is very fine (between 0.45 and 50 μm). The high biomass also explains the presence of abundant filter-feeders, such as Hydropsyche and Ephoron virgo. In some parts, where light reaches the bottom, stones and boulders are covered by Cladophora. In this case, grazers such as the gastropods Melanopsis and Theodoxus are abundant.