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 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Multi-walled carbon nanotubes (MWNTs) without any metal ions were used as the catalyst, and investigated in the CWAO of phenol and aniline in a batch reactor. The structures of the MWNTs were characterized by means of SEM and TEM. It showed that the MWNTs, treated with the mixed acid (HNO3-H2SO4), displayed excellent activity and stability in the CWAO. Under the reaction temperature of 160 degrees C, the total pressure of 2.5 MPa, the initial concentration of 1000 mg/L and loading the catalyst of 1.6 g/L, 100% phenol and 86% COD were removed after 120 min reaction in CWAO of phenol. At the same operating conditions, 83% aniline and 68% COD removals were obtained in the CWAO of aniline solution when the initial concentration of aniline was 2 000 mg/L. The surface functional groups played the important role for the high activity of the MWNTs in CWAO of organic compounds.
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PMID:[Catalytic wet air oxidation of phenol and aniline over multi-walled carbon nanotubes]. 1906 37

This paper presents a new way of recycling aluminum and iron in boiler slag derived from coal combustion plants, which integrates efficient extraction and reuse of the leached pellets together. The boiler slag was pelletized together with washed coal and lime prior to sintering and then was sintered at 800-1200 degrees C for different periods to produce sintered pellets for the leaching test. An elemental analysis of aqueous solutions leached by sulfuric acid was determined by EDTA-Na(2)-ZnCl(2) titration method. The components and microstructures of the samples, sintered pellets and leached residue were examined by means of XRF, XRD and SEM. XRD analysis indicates that predominate minerals such as kaolinite, quartz, calcium silicide, hematate and metakoalin exist in the boiler slag. An aluminum extraction efficiency of 86.50% was achieved. The maximum extraction efficiency of Fe was 94.60% in the same conditions of that for the maximum extraction efficiency of Al. The extraction efficiencies of Al and Fe increased with an increase in temperature, leaching time and acidity. High Al extraction efficiency was obtained for pellets with high CaO content. The final product of alumina would be used directly for the production of metallic aluminum.
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PMID:Leaching of aluminum and iron from boiler slag generated from a typical Chinese Steel Plant. 1915 93

Vertically-oriented high aspect ratio titania nanotube bundles have been grown by a potentiostatic anodization of titanium sheet in fluoride-free electrolytes. The anodization conditions like the applied voltage were optimized for the synthesis of titania nanotubes in HClO4 and NaCl electrolyte. The resulting nanotubes have a length of about 30 microm, outer diameter about 40 nm, inner pore size of about 10 nm and the aspect ratio was 750:1 by anodization in 0.1 M perchloric acid of pH approximaately 1 at applied voltage of 20 V. While for nanotubes prepared in 0.3 M NaCl of pH 4.3, the length was above 50 microm with the aspect ratio of 1250:1. A method to increase the uniformity of nanotube was demonstrated by pretreatment the titanium sheet by (4 wt% HF + 5 M HNO3) solution prior to anodization. Titania nanotubes were prepared, for the first time, by anodization in aqueous H2SO4 electrolyte alone with tube length above 500 nm. Annealing studies were performed, on high aspect ratio Titania nanotube layers produced in HClO4 electrolyte, in the temperature interval of 300 to 550 degrees C. The XRD patterns and TEM data confirmed the formation of single anatase phase after annealing at 450 degrees C with perfect nanoubular structure. While the rutile titania phase starts to emerege after annealing at about 500 degrees C and the evidence for the appearance of rutile phase due to the oxidation of the underlying Ti metal at the interface between nanotube/Ti-metal was given. On the other hand, the nanotubular structure starts to destroy upon annealing temperature of approximate 550 degrees C by tube flattening and losing of roll-up characteristics as indicated in SEM images. The superior morphology of these high aspect ratio nanotubes and their rapid growth rate foreshadow a bright future in wide applications like dye-sensitized solar cells, water photolysis and nanobiomedical.
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PMID:Electrochemical growth of vertically-oriented high aspect ratio titania nanotubes by rabid anodization in fluoride-free media. 1943 43

Using sludge as pore-forming agent, bentonite granule was acidified by sulfuric acid solution as a decolorant. The specific surface area and SEM were performed to characterize the structure of samples, and the new acidified sludge-bentonite granule was applied to the decoloration of reactive turquoise blue. The influencing factors of pH value, dosage, reaction time and reaction temperature were studied on the removal of the dyes. The important thermodynamics parameters (DeltaH0, DeltaS0, DeltaG) and the activation energy Ea were also acquired by experiment data processing. The results indicated that the adsorption isotherm fitted the isothermal adsorption equations of Langmuir better than Freundlich. The adsorption dynamics followed the law of the pseudo-second order kinetic equation, while the adsorption rate is 313 K > 303 K > 293 K. The low value of Ea which is 5.52 kJ x mol(-1) shows that physical adsorption is primary. And DeltaH0 > TDeltaS0 means that the influence of enthalpy is more remarkable than the entropy in the activation reaction. DeltaG > 0 also means the chemical reactions are not spontaneous.
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PMID:[Decoloration of reactive turquoise blue by acidified sludge-bentonite granule]. 1955 23

Acid tars from the processing of petroleum and petrochemicals using sulfuric acid were characterized by gas chromatography/mass spectrometry (GC/MS), inductively coupled plasma/optical emission spectrometry (ICP/OES), differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectrometry, and scanning electron microscopy/energy dispersive X-ray (SEM/EDX) micro-analysis. Leaching of contaminants from the acid tars in 48 h batch tests with distilled water at a liquid-to-solid ratio 10:1 was also studied. GC/MS results show that the samples contained aliphatic hydrocarbons, cyclic hydrocarbons, up to 12 of the 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs), and numerous other organic groups, including organic acids (sulfonic acids, carboxylic acids and aromatic acids), phenyl, nitrile, amide, furans, thiophenes, pyrroles, and phthalates, many of which are toxic. Metals analysis shows that Pb was present in significant concentration. DSC results show different transition peaks in the studied samples, demonstrating their complexity and variability. FTIR analysis further confirmed the presence of the organic groups detected by GC/MS. The SEM/EDX micro-analysis results provided insight on the surface characteristics of the samples and show that contaminants distribution was heterogeneous. The results provide useful data on the composition, complexity, and variability of acid tars; information which hitherto have been scarce in public domain.
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PMID:Characterization of acid tars. 1985 24

The purpose of this study was the synthesis of two thiol conjugated Chitosan polymers, and evaluation of the potential of Thiomer nanoparticle formulation as a carrier for oral delivery system. Mediated by EDAC (Ethylene-3-(3-di-methylaminopropyl)-carbodiimide), either N-acetyl Cysteine (NAC) or N-acetyl D-penicillamine (NAP) were covalently attached to Chitosan. The success of the synthesis was demonstrated by comparing FTIR spectra. Iodometric titration demonstrated that depending on the pH value of the synthesis medium, the Thiomers display 250 +/- 30 microMol and 300 +/- 20 microMol thiol groups per gram of polymer respectively. The interaction between mucin and Thiomers, compared to mucin and Chitosan was studied for assessment of mucoadhesion properties of synthesized polymers. This interaction was determined by the measurement of the amount of mucin adsorbed on Chitosan and the conjugated polymers. Rotating cylinder method demonstrated an average of 20 times improvement in mucoadhesion of Thiomers compared to the unmodified polymer. Chitosan and Thiomer nanoparticles were formulated by two methods; TPP and Sodium Sulfate gelation. SEM micrographs and data achieved by a Malvern nano/zetasizer show nanoparticles formed by TPP gelation have a mean size of 150 +/- 15 nm compared to 300 +/- 25 nm sized nanoparticles obtained by Sodium sulfate gelation. TPP gelation yields smaller, more spherical shaped nanoparticles with a smaller range of size distribution. Amikacin loaded nanoparticles with an average size of 280 nm were prepared by TPP gelation in which disulfide bond formation was achieved by a time dependent oxidation process. In vitro studies were carried out; a recovery rate of 33% and a drug entrapment of 25% were achieved. The amount of release was determined during 18 hr in a carefully prepared media. The permeation time across a biological membrane was observed to be about 150 minutes. Microbiological tests were carried out on two microorganisms; Pseudomona aeruginosa and Staphylococcus aureus to further confirm the amount of Amikacin inside drug loaded nanoparticles.
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PMID:Thiolated chitosan nanoparticles as an oral delivery system for Amikacin: in vitro and ex vivo evaluations. 1992 23

Cellulose triacetate was prepared via reacting of a mixture of acetic anhydride and acetic acid containing sulfuric acid as catalyst with ramie fiber obtained from a biomass of ramie. The cellulose triacetate with a degree of substitution (DS) 2.93 of the ramie fiber was obtained. The honeycomb-like cellulose triacetate microspheres with an average diameter of 14 microm were made from the cellulose triacetate solution. The optimum conditions for preparing the microspheres were determined as cellulose triacetate/dichloromethane ratio 1:7 (w/w), and 0.75% sodium dodecylsulfonate. The cellulose triacetate microspheres were characterized using FT-IR, NMR, XRD, and SEM. Application of the microspheres as an adsorbent for removing disperse dyes in water was investigated under the temperatures from 15 to 50 degrees C, pHs from 4 to 9, and the weight of cellulose triacetate microspheres from 0.03 to 0.09 g. The cellulose triacetate microspheres exhibited a 16.5mg/g capability to remove DR dye from water at 50 degrees C and pH 7.
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PMID:Preparation and application of cellulose triacetate microspheres. 2006 Jun 44

Three different pretreatment methods for switchgrass were studied. Aqueous sodium hydroxide (0.5-10% w/v, 90 degrees C, 1h), dilute H(2)SO(4) (0.5-6.0% v/v, 121 degrees C, 1h) and hot water (100 degrees C, 1h) were employed in this study to determine how each method affected the digestibility of switchgrass during enzymatic hydrolysis. Switchgrass pre-treated with 0.5% w/v sodium hydroxide generally produced glucose in higher concentrations than sulfuric acid and hot water pre-treated samples. SEM studies on the pre-treated samples revealed a great deal of pore formation in the NaOH pre-treated samples and little or no physical changes on the acid and hot water pre-treated samples. Lignin analysis carried out on the pre-treated samples showed a considerable decrease in lignin content in the NaOH pre-treated samples and only a slight decrease in lignin content for the other pretreatment methods studied.
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PMID:Comparison of different pretreatment methods based on residual lignin effect on the enzymatic hydrolysis of switchgrass. 2021 64

To study and evaluate the performance of the continuously-operated autohydrogenotrophic sulfate reduction technique enhanced with electrochemical method and to improve the sulfate removal efficiency, a combined bio-electrical sulfidogenic system was developed with a three-dimensional bio-cathode. Sulfate reduction rate was elevated markedly owing to H2 mass transfer enhancement, biomass augmentation and electrical field stimulation. Indeed, when a current of 0.50 mA was applied to the system, the average sulfate removal load was 1.94 g/(L x d) during the stable running status and the maximum removal load was 2.23 g/(L x d). Furthermore, the combined bio-electrical system was comparatively more stable in terms of response to the variation of influx load under the same hydraulic conditions. Results of SEM showed that besides the bacteria attached on the surface of the hollow fiber, large amount of biomass was aggregated on the surface and the inner gridding space of the graphite felt. PCR-DGGE analysis indicated that the diversity of the microbial community structure was slightly reduced resulting in an optimized one. The dominant genera were Desulfovibrio and Desulfomicrobium. Enhanced H2 mass transfer, biomass augmentation, optimized microbial community structure and electrical stimulation were the key important factors for the high sulfate reduction efficiency of the system.
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PMID:[Performance of a combined bio-chemical sulfidogenic system and microbial characteristics in the presence of H2]. 2035 31

In this work, radiological, chemical, and also morphological characterization was performed in phosphate rock and phosphogypsum samples, in order to understand the behavior of toxic elements. Characterization was carried out using X-ray diffraction (XRD), X-ray fluorescence (XRF), gamma spectrometry and scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDX). Our results show that the phosphate rock was mainly composed of fluorapatite, calcite, perovskite, quartz, magnetite, pyrite and kaolinite, whereas phosphogypsum only exhibited dihydrated calcium sulfate. The activity concentration of U-series radioisotopes in phosphate rock was around 1640 Bq/kg. (226)Ra and (210)Pb tend to be distributed into phosphogypsum by up to 80%, whereas the fraction of U-isotopes is 10%. The most abundant trace elements in phosphate rock were Sr, Cr, V, Zn, Y, Ni and Ba. Some elements, such as Ba, Cd, Cu, La, Pb, Se, Sr, Th and Y, were enriched in the phosphogypsum. This enrichment may be attributed to an additional input associated to the sulfuric acid used for the phosphoric acid production. Furthermore, results from SEM-EDX demonstrated that toxic elements are not distributed homogeneously into phosphogypsum. Most of these elements are concentrated in particles <20 microm of high porosity, and could be easily mobilized by leaching and/or erosion.
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PMID:Radiological, chemical and morphological characterizations of phosphate rock and phosphogypsum from phosphoric acid factories in SW Spain. 2053 94


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