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.     

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.     

Sodium Alginate—Natural Microencapsulation Material of Polymeric Microparticles

From the multitude of materials currently available on the market that can be used in the development of microparticles, sodium alginate has become one of the most studied natural anionic polymers that can be included in controlled-release pharmaceutical systems alongside other polymers due to its low cost, low toxicity, biocompatibility, biodegradability and gelatinous die-forming capacity in the presence of Ca²⁺ ions. In this review, we have shown that through coacervation, the particulate systems for the dispensing of drugs consisting of natural polymers are nontoxic, allowing the repeated administration of medicinal substances and the protection of better the medicinal substances from degradation, which can increase the capture capacity of the drug and extend its release from the pharmaceutical form.     

Rich Phase Behavior in a Supramolecular Conducting Material Derived from an Organogelator

Organic conducting fiber‐like materials hold great promise for the development of nanowires that can act as connections in miniature electronic devices, as an alternative to inorganic nanometer scale structures. This article presents a conducting organic tetrathiafulvalene‐based supramolecular material which possesses a rich phase behavior with different packing of the molecules in the different forms, evidenced by electron spin resonance (ESR) spectroscopy. The distinct phases of conducting nanofibers can be easily fabricated through the temperature control of their preparation process from a xerogel by doping with iodine vapors. A total of four conducting phases have been identified conclusively using ESR spectroscopy as the key analytical tool. Three of the phases show a good long‐term stability and areas in which the I–V curves have ohmic behavior when studied by current sensing (conducting) AFM. They offer promise for applications where electrical nanometer scale connections are required.     

Scandium Recovery from Aqueous Solution by Adsorption Processes in Low-Temperature-Activated Alumina Products

In this paper, we studied the scandium adsorption from aqueous solutions on the surface of low-temperature-activated alumina products (GDAH). The GDAH samples are industrially manufactured, coming from the Bayer production cycle of the Sierra Leone bauxite as aluminium hydroxide, and further, by drying, milling, classifying and thermally treating up to dehydroxilated alumina products at low temperature. All experiments related to hydroxide aluminium activation were conducted at temperature values of 260, 300 and 400 °C on samples having the following particle sizes: <10 µm, 20 µm, <45 µm and <150 µm, respectively. The low-temperature-activated alumina products were characterised, and the results were published in our previous papers. In this paper, we studied the scandium adsorption process on the above materials and related thermodynamic and kinetic studies.