Acid Black 194 Dye Clarifications Onto Natural And Acid/Base Activated Smectitic Clays

The present work is concerned the Acid Black 194 dye adsorption by Two smectitic clays (BJ and AJ) aged upper Eocene were sampled from Atlas Central of Tunisia in Kairouan region. Technical characterization was carried out using calcimetry and X-ray diffraction. The activation studies of clays by HCl/ Na2CO3 have been conducted to improve their physicochemical properties. The optimum result of the surface area after acid activation (aa) was 398 m2/g for BJ aa and AJ aa, after basic activation (ab) the surface area was 460 m2 /g for BJ ab and 440 m2/g for AJ ab. The characterization by XRD, chemical analysis and SEM observations, were performed before and after optimum activation.Moreover, the raw and activated samples (aa/ab) under the optimum activation conditions were used in the effluent treatment. Adsorption tests were made by batch system at 25 °C in different pH (2-12) and by varying the adsorbent amount (0.025-0.1 g). The best adsorption results were recorded with pH = 11 and amount adsorbent 0.025 g. The raw clay adsorption capacity was slightly better than activated samples. The best yield was given by BJ (94%). Therefore, clay can be used in various applications without any characteristic modification.

A Kinetic Study of 2-Amino-4-(Methyl-Thio) Butanoic Acid By Quinaldinium Fluorochromate In Selected Hydrophilic Solvent Medium

A Major role in oxidation kinetics is to determine the reaction mechanism that comprise chemical reaction. In the present paper we derived rate law for reaction mechanism and to recognized the order of reaction, give rate equation, calculate the rate constant. Identify the product of this oxidation reaction.The chemical oxidation of 2-Amino-4-methyl thio-butanoic acid by Quinaldinium Fluorochromate was studied in 50-50 (v/v) selected hydrophilic solvent medium at 308 Kelvin. The reaction is acid catalysed and exhibits first order dependence with respect to oxidant, substrate, and fractional order respect to H+ ion concentrations. Chemical oxidation kinetics is the study of the rate of chemical reaction.the factors Manganesh sulphate, Acrylonitrile, Sodium perchlorate that affect these rates (or) not, and draw of ln Kobs/T verses 1/T energy diagram to find the activation energy. Addition of sodium perchlorate slightly decreases the rate of reaction. However, Acrylonitrile is not induced by the polymerization reaction, showing that there is no free radical route. Added Mn2+ increases with slightly increase rate in the reaction medium. 2-Amino-4-(MethylThio)-Butanoic acid by Quinaldinium Fluorochromate has not been reported. Hence, the investigation of oxidation of 2-Amino-4-Methyl Thio-Butanoic acid by QNFC in selected hydrophilic solvent medium and the corresponding mechanistic aspects are discussed in this research paper. A systematic kinetic work carried out to explore the physical characterization of the reactance. The characterstic effects like Substrate, Oxidant, Perchloric acid, Solvent, Sodium perchlorate, Acrylonitrile, Manganes sulphate and Influence Temperature it clearly shows effect on that reaction path. The process was carried out at four different temperatures to determine the activation conditions. The measured kinetic findings ΔH# and ΔS# are derived from the value.

Geranylgeraniol Restores Zoledronic Acid-Induced Efferocytosis Inhibition in Bisphosphonate-Related Osteonecrosis of the Jaw

Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is a severe side effect of long-term administration of bisphosphonates such as zoledronic acid (ZA), but its pathogenesis remains unclear. Impairment of the clearance of apoptotic cells (termed “efferocytosis”) by ZA may be associated with the pathogenesis of BRONJ. The aim of this study was to investigate whether ZA might inhibit macrophage efferocytosis and promote osteocytic apoptosis, and the underlying mechanisms responsible for the disturbing balance between clean and generation of osteocytic apoptosis. We found that ZA significantly promoted the apoptosis of osteocyte and pre-osteoblast via BRONJ mouse models and in vitro MC3T3-E1 but also inhibited the efferocytosis of macrophage on apoptotic cells. Moreover, supplement with geranylgeraniol (GGOH), a substrate analog for geranylgeranylation of Rac1, could restore Rac1 homeostasis and rescue macrophage efferocytosis. GGOH partially inhibits MC3T3-E1 apoptosis induced by ZA via downregulation of Rac1/JNK pathway. We also examined the Rac1 distribution and activation conditions in bone marrow-derived macrophages (BMDMs) and MC3T3-E1 under ZA treatment, and we found that ZA impaired Rac1 migration to BMDM membrane, leading to round appearance with less pseudopodia and efferocytosis inhibition. Moreover, ZA simultaneously activated Rac1, causing overexpression of P-JNK and cleaved caspase 3 in MC3T3-E1. Finally, the systemic administration of GGOH decreased the osteocytic apoptosis and improved the bone healing of the extraction sockets in BRONJ mouse models. Taken together, our findings provided a new insight and experimental basis for the application of GGOH in the treatment of BRONJ.

Verified Lustre Normalization with Node Subsampling

Dataflow languages allow the specification of reactive systems by mutually recursive stream equations, functions, and boolean activation conditions called clocks. Lustre and Scade are dataflow languages for programming embedded systems. Dataflow programs are compiled by a succession of passes. This article focuses on the normalization pass which rewrites programs into the simpler form required for code generation. Vélus is a compiler from a normalized form of Lustre to CompCert’s Clight language. Its specification in the Coq interactive theorem prover includes an end-to-end correctness proof that the values prescribed by the dataflow semantics of source programs are produced by executions of generated assembly code. We describe how to extend Vélus with a normalization pass and to allow subsampled node inputs and outputs. We propose semantic definitions for the unrestricted language, divide normalization into three steps to facilitate proofs, adapt the clock type system to handle richer node definitions, and extend the end-to-end correctness theorem to incorporate the new features. The proofs require reasoning about the relation between static clock annotations and the presence and absence of values in the dynamic semantics. The generalization of node inputs requires adding a compiler pass to ensure the initialization of variables passed in function calls.

Durability of Sustainable Ceramics Produced by Alkaline Activation of Clay Brick Residue

Alkali-activated materials (AAMs) were produced using residues from the red ceramic industry as a precursor, and sodium hydroxide (NaOH), potassium hydroxide (KOH), and sodium silicate (Na2SiO3) as alkaline activators. The effect of activators and curing conditions on physical-mechanical properties and durability were evaluated. The processing parameters (amount of water and consistency index) and the activation conditions (the activator contents and curing temperature) were defined based on an experimental design getting the flexural rupture module as the response. The durability behavior was evaluated by natural aging, accelerated aging (simulated rain test), exposure to the marine environment (salt fog), and acidic environments (HCl and H2SO4). The results showed that the NaOH- and KOH-activated samples exhibited inferior mechanical behavior than those activated with Na2SiO3. In the durability studies, due to leaching, there was a decrease in mechanical strength when samples are subjected to aggressive exposure conditions. However, the strength values are still higher than the minimum indicated for traditional ceramic applications.

INF2-mediated actin filament reorganization confers intrinsic resilience to neuronal ischemic injury

During early stages of ischemic brain injury, glutamate receptor hyperactivation mediates neuronal death via osmotic cell swelling. Here we show that ischemia and excess NMDA receptor activation, conditions that trigger neuronal swelling, cause actin filaments to undergo a rapid and extensive reorganization within the somatodendritic compartment. Normally, Factin is concentrated within dendritic spines, with relatively little Factin in the dendrite shaft. However, beginning <5 min after incubation of neurons with NMDA, Factin depolymerizes within dendritic spines and polymerizes into long, stable filament bundles within the dendrite shaft and soma. A similar actinification of the somatodendritic compartment occurs after oxygen/glucose deprivation in vitro, and in mouse brain after photothrombotic stroke in vivo. Following transient, sub-lethal NMDA exposure these actin changes spontaneously reverse within 1-2 hours. A combination of Na+, Cl-, water, and Ca2+ entry are all necessary, but not individually sufficient, for induction of actinification. Spine F-actin depolymerization is also required. Actinification is driven by activation of the Factin polymerization factor inverted formin2 (INF2). Silencing of INF2 renders neurons more vulnerable to NMDA induced membrane leakage and cell death, and formin inhibition markedly increases ischemic infarct severity in vivo. These results show that ischemia induced actin filament reorganization within the dendritic compartment is an intrinsic pro-survival response that protects neurons from death induced by swelling.

Nanoporous Carbon Magnetic Hybrid Derived From Waterlock Polymers and Its Application for Hexavalent Chromium Removal from Aqueous Solution

Sodium polyacrylate is the superabsorbent waterlock polymer used in disposable diapers, which are the third largest single consumer item in landfills. As diapers are difficult to recycle, their use produces an incredible amount of environmental waste. In the present article, we present a reliable and facile approach to transform sodium polyacrylate, the main constitute in the used diapers, in a carbon-based magnetic sorbent material, capable for use in environmental applications. A nanoporous carbon magnetic hybrid material was prepared by reacting NaPA with iron acetate species under chemical activation conditions. Analysis of the characterization results revealed, the creation of a nanoporous structure, with high specific surface area value (SgBET = 611 m2/g), along with the formation of nanosized zero valent iron nanoparticles and iron carbide (Fe3C), inside the carbon pore system. 57Fe Mössbauer spectroscopy verified also the existence of these two main iron-bearing phases, as well as additional minor magnetic phases, such as Fe3O4 and γ-Fe2O3. Vibrating sample magnetometry (VSM) measurements of the obtained hybrid confirmed its ferromagnetic/ferrimagnetic behavior. The hybrid material demonstrated a rapid sorption of Cr(VI) ions (adsorption capacity: 90 mg/g, 24 h pH = 3). The results showed highly pH-dependent sorption efficiency of the hybrids, whereas a pseudo-second-order kinetic model described their kinetics.

The Analysis of Pore Development and Formation of Surface Functional Groups in Bamboo-Based Activated Carbon during CO2 Activation

Pore development and the formation of oxygen functional groups were studied for activated carbon prepared from bamboo (Bambusa bambos) using a two-step activation with CO2, as functions of carbonization temperature and activation conditions (time and temperature). Results show that activated carbon produced from bamboo contains mostly micropores in the pore size range of 0.65 to 1.4 nm. All porous properties of activated carbons increased with the increase in the activation temperature over the range from 850 to 950 °C, but decreased in the temperature range of 950 to 1000 °C, due principally to the merging of neighboring pores. The increase in the activation time also increased the porous properties linearly from 60 to 90 min, which then dropped from 90 to 120 min. It was found that the carbonization temperature played an important role in determining the number and distribution of active sites for CO2 gasification during the activation process. Empirical equations were proposed to conveniently predict all important porous properties of the prepared activated carbons in terms of carbonization temperature and activation conditions. Oxygen functional groups formed during the carbonization and activation steps of activated carbon synthesis and their contents were dependent on the preparation conditions employed. Using Boehm’s titration technique, only phenolic and carboxylic groups were detected for the acid functional groups in both the chars and activated carbons in varying amounts. Empirical correlations were also developed to estimate the total contents of the acid and basic groups in activated carbons in terms of the carbonization temperature, activation time and temperature.

Synthesis of 5-arylacetylenyl-1,2,4-oxadiazoles and their transformations under superelectrophilic activation conditions

Acetylene derivatives of 1,2,4-oxadiazoles, i.e., 5-(2-arylethynyl)-3-aryl-1,2,4-oxadiazoles, have been obtained, for the first time reported, from 5-(2-arylethenyl)-3-aryl-1,2,4-oxadiazoles by their bromination at the carbon–carbon double bond followed by di-dehydrobromination with NaNH2 in liquid NH3. The reaction of the acetylenyl-1,2,4-oxadiazoles with arenes in neat triflic acid TfOH (CF3SO3H) at room temperature for 1 h resulted in the formation of E/Z-5-(2,2-diarylethenyl)-3-aryl-1,2,4-oxadiazoles as products of regioselective hydroarylation of the acetylene bond. The addition of TfOH to the acetylene bond of these oxadiazoles quantitatively resulted in E/Z-vinyl triflates. The reactions of the cationic intermediates have been studied by DFT calculations and the reaction mechanisms are discussed.