Synthesis and dissolution behavior of nanosized silicon and magnesium co-doped fluorapatite obtained by high energy ball milling

Nanosized hydroxyapatite (HA) powders exhibit a greater surface area than coarser crystals and are expected to show an improved bioactivity. In addition, properties of HA can be tailored over a wide range by incorporating different ions into HA lattice. The aim of this study was to prepare and characterize silicon and magnesium co-doped fluorapatite (Si–Mg–FA) with a chemical composition of Ca_9.5Mg_0.5 (PO₄)_5.5(SiO₄)_0.5F₂ by the high-energy ball milling method. Characterization techniques such as X-ray diffraction analysis (XRD), Fourier transformed infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX) and transmission electron microscopy (TEM) were utilized to investigate the structural properties of the obtained powders. Dissolution behavior was evaluated in simulated body fluid (SBF) and physiological normal saline solution at 37 °C for up to 28 days. The results of XRD and FTIR showed that nanocrystalline single-phase Si–Mg–FA powders were synthesized after 12 h of milling. In addition, incorporation of magnesium and silicon into fluorapatite lattice decreased the crystallite size from 53 nm to 40 nm and increased the lattice strain from 0.220% to 0.296%. Dissolution studies revealed that Si–Mg–FA in comparison to fluorapatite (FA), releases more Ca, P and Mg ions into SBF during immersion. 175 ppm Ca, 33.5 ppm P and 48 ppm Mg were detected in the SBF containing Si–Mg–FA after 7days of immersion, while for FA, it was 75 ppm Ca, 21.5 ppm P and 29 ppm Mg. Release of these ions could improve the bioactivity of the obtained nanopowder. It could be concluded that the prepared nanopowders have structural properties such as crystallite size (~40 nm), crystallinity degree (~40%) and chemical composition similar to biological apatite. Therefore, prepared Si–Mg–FA nanopowders are expected to be appropriate candidates for bone substitution materials and also as a phase in polymer or ceramic-based composites for bone regeneration in tissue engineering applications.     

Effect of green manure and supplemental fertility amendments on selected soil quality parameters in an organic potato rotation in Eastern Canada

The effects of green manure, crop sequence and off-farm composts on selected soil quality parameters were assessed in a three-year organic potato (Solanum tuberosum L.) rotation in Eastern Canada. Three crop sequences varying in preceding green manure [red clover (RCl) + RCl, and beans/buckwheat or carrots + oats/peas/vetch mixture (OPV)] as main plots and four fertility treatments applied in the potato phase only [control; inorganic fertilizer; municipal solid waste compost (MSW); composted paper mill biosolid (PMB)] as subplots were compared. In 2008 and 2010, changes in selected soil quality parameters (0–15 cm) were assessed prior to planting of potatoes and at potato tuber initiation stage. Potentially mineralizable nitrogen (N) and the acid phosphatase enzyme activity average values across years were greater following RCl (1.51 abs and 622 kg ha^?1) compared with OPV (1.32 abs and 414 kg ha^?1) at potato planting. Soil NO₃–N average value was greater following RCl compared with OPV (63 vs. 52 kg ha^?1) at tuber initiation. For the other measured parameters, OPV and RCl were similar. The soil organic carbon (C) and particulate organic matter-C were greater under PMB and MSW (31.1 and 7.57 kg ha^?1) compared with fertilizer treatment (27.9 and 6.05 kg ha^?1). The microbial biomass C and microbial biomass quotient were greater under MSW (216 kg ha^?1 and 0.73 %) than PMB and fertilizer (147 kg ha^?1 and 0.50 %) across crop rotations. Annual legume green manures and off-farm composts can be used to satisfy potato N requirement and maintains soil quality in organic potato rotations.     

Prediction of hydrate equilibrium conditions using k-nearest neighbor algorithm to CO2 capture

Gas or clathrate hydrates are an important issue when they form in the oil and gas pipelines. Since the determination of the hydrate formation temperature and pressure is very difficult experimentally for every gas system and it is impossible in terms of cost and time approximately, mathematical models can be useful tools to overcome these difficulties. In this study, k-nearest neighbor model was used to predict the equilibrium conditions of hydrate formation in absorption and separation of carbon dioxide from flue gas mixture, containing carbon dioxide and nitrogen. At the training phase, temperature and composition data of nitrogen and carbon dioxide in the flue gas mixture at equilibrium conditions and the equilibrium pressures of hydrate formation were used as input and output, respectively. The error percentage less than 0.38% indicates the high accuracy of the proposed model. In this study, 80%, 85%, and 90% of the training data are examined for three numbers of nearest. For three numbers of used nearest (k = 1, k = 2 and k = 3), the value of k = 1 leads to the lowest error; so, it is selected as the best nearest in the presented model.     

The preparation of an amino acid-based surfactant and its potential application as an EOR agent

Most of the synthetic surfactants investigated with the aim of enhanced chemically oil recovery in the literature have environmental drawbacks. In this work, application of an environmentally-friendly synthetic surfactant as an enhanced oil recovery agent is introduced by measuring interfacial tension of water–kerosene systems and wettability alteration of carbonate pellets. For this purpose, an amino acid-based surfactant was initially synthesized using a new synthetic approach which was subsequently confirmed by spectra of Fourier transform infrared and Proton nuclear magnetic resonance. Results showed a value of critical micelle concentration in the range of 9000–9100 ppm for this surfactant. Results also demonstrated a decrease of 38.53% in water–kerosene system interfacial tension and a 17.76% reduction in oil-wetness of the carbonate pellets.     

Simple N‐Heterocyclic Carbenes as Ligands in Ullmann‐Type Ether and Thioether Formations

A simple N‐heterocyclic carbene (NHC) derived from 1‐methyl‐3‐ethylimidazolium tetrafluoroborate was found to be an efficient ligand for a range of copper‐catalyzed cross‐coupling reactions, leading to the formation of aromatic ethers and thioethers.

     

Gate All Around Dopingless Nanotube TFET Biosensor with Si0.5Ge0.5 – Based Source

Silicon - Through this paper, we discuss how Tunnel Field Effect Transistors can be utilized for the detection of biomaterials hence acting as a biosensor. The device proposed is a 3-D Doping less...     

Cement take estimation using neural networks and statistical analysis in Bakhtiari and Karun 4 dam sites,in south west of Iran

Bulletin of Engineering Geology and the Environment - Water seepage from dam foundations causes reservoir water loss and raises the risk of dam instability. One method of remediation for...     

Crystal Structure and Physicochemical Properties of Two Supramolecular Compounds: (C4H8NH2)4[Mo8O26] and (NH4)Na2[AsIIIMo6O21(O2CCH2NH3)3]·8H2O

Two inorganic–organic hybrid supramolecular compounds based on polyoxometalates formulated as (C₄H₈NH₂)₄[Mo₈O₂₆] (1) and (NH₄)Na₂[As^IIIMo₆O₂₁(O₂CCH₂NH₃)₃]·8H₂O (2) have been synthesized by conventional solution method and characterized by infrared, UV–Vis and single-crystal X-ray diffraction analyses. Thermal analysis was performed to study their thermal stability. The atomic arrangement in compound (1) can be described as inorganic layers built by [Mo₈O₂₆]^4?, pyrrolidinium cations are embedded into layers. The fascinating structural feature of compound (2) is that the glycine molecules are bounded to two edge-sharing Mo centers via their carboxylate functionality leading to functionalized heteropolymolybdate [As^IIIMo₆O₂₁(O₂CCH₂NH₃)₃]^3?, extensive net hydrogen bonds between cations and anions contribute to the crystal packing. The electrochemical behavior of compound (2) has been studied.     

Understanding the Corrosion Inhibition Mechanism of Mild Steel in Hydrochloric Acid by a Triazole Derivative: A Combined Experimental and Theoretical Approach

Protection of Metals and Physical Chemistry of Surfaces - The effect of an heterocycle triazole, namely (1-(4-methoxyphenyl)-1H-1,2,3-triazol-4-yl)methanol (MTM) on the corrosion of mild steel in...     

Inhibition of Listeria monocytogenes and Salmonella by Combinations of Oriental Mustard,Malic Acid,and EDTA

The antimicrobial activities of oriental mustard extract alone or combined with malic acid and EDTA were investigated against Salmonella spp. or Listeria monocytogenes at different temperatures. Five strain Salmonella or L. monocytogenes cocktails were separately inoculated in Brain Heart Infusion broth containing 0.5% (w/v) aqueous oriental mustard extract and incubated at 4 °C to 21 °C for 21 d. For inhibitor combination tests, Salmonella Typhimurium 02:8423 and L. monocytogenes 2–243 were individually inoculated in Mueller Hinton broth containing the mustard extract with either or both 0.2% (w/v) malic acid and 0.2% (w/v) EDTA and incubated at 10 °C or 21 °C for 10 to 14 d. Mustard extract inhibited growth of the L. monocytogenes cocktail at 4 °C up to 21 d (2.3 log₁₀ CFU/mL inhibition) or at 10 °C for 7 d (2.4 log₁₀ CFU/mL inhibition). Salmonella spp. viability was slightly, but significantly reduced by mustard extract at 4 °C by 21 d. Although hydrolysis of sinigrin in mustard extract by both pathogens was 2 to 6 times higher at 21 °C than at 4 °C to 10 °C, mustard was not inhibitory at 21 °C, perhaps because of the instability of its hydrolysis product (allyl isothiocyanate). At 21 °C, additive inhibitory effects of mustard extract with EDTA or malic acid led to undetectable levels of S. Typhimurium and L. monocytogenes by 7 d and 10 d, respectively. At 10 °C, S. Typhimurium was similarly susceptible, but combinations of antimicrobials were not more inhibitory to L. monocytogenes than the individual agents.