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1.
Bioresour Technol ; 129: 612-5, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23337539

ABSTRACT

The existing water treatment process often uses chemicals, which is of high health and environmental concern. The present study focused on the efficiency of microemulsion prepared magnetic iron oxide nanoparticles (ME-MIONs) and protein-functionalized nanoparticles (MOCP+ME-MIONs) in water treatment. Their influence on mineral ions and microorganisms present in the surface water from lake Brunnsviken and Örlången, Sweden were investigated. Ion analysis of water samples before and after treatment with nanoparticles was performed. Microbial content was analyzed by colony forming units (CFU/ml). The results impart that ME-MIONs could reduce the water turbidity even in low turbid water samples. Reduction of microbial content (98%) was observed at 37°C and more than 90% reduction was seen at RT and 30 °C when compared to untreated samples from lake Örlången. The investigated surface water treatment method with ME-MIONs was not significantly affecting the mineral ion composition, which implies their potential complement in the existing treatment process.


Subject(s)
Minerals/chemistry , Moringa oleifera/chemistry , Plant Proteins/chemistry , Water Microbiology , Water Pollutants, Chemical/chemistry , Water Purification/methods , Magnetite Nanoparticles , Minerals/isolation & purification , Water Pollutants, Chemical/isolation & purification
2.
J Chromatogr A ; 1247: 134-45, 2012 Jul 20.
Article in English | MEDLINE | ID: mdl-22687712

ABSTRACT

An on-line gas chromatographic (GC) system has been developed for rapid and accurate product analysis in catalytic conversion of syngas (a mixture of H2 and CO) to alcohols, so called "higher alcohol synthesis (HAS)". Conversion of syngas to higher alcohols is an interesting second step in the route of converting coal, natural gas and possibly biomass to liquid alcohol fuel and chemicals. The presented GC system and method are developed for analysis of the products formed from syngas using alkali promoted MoS2 catalysts, however it is not limited to these types of catalysts. During higher alcohol synthesis not only the wanted short alcohols (∼C2-C5) are produced, but also a great number of other products in smaller or greater amounts, they are mainly short hydrocarbons (olefins, paraffins, branched, non-branched), aldehydes, esters and ketones as well as CO2, H2O. Trace amounts of sulfur-containing compounds can also be found in the product effluent when sulfur-containing catalysts are used and/or sulfur-containing syngas is feed. In the presented GC system, most of them can be separated and analyzed within 60 min without the use of cryogenic cooling. Previously, product analysis in "higher alcohol synthesis" has in most cases been carried out partly on-line and partly off-line, where the light gases (gases at room temp) are analyzed on-line and liquid products (liquid at room temp) are collected in a trap for later analysis off-line. This method suffers from many drawbacks compared to a complete on-line GC system. In this paper an on-line system using an Agilent 7890 gas chromatograph equipped with two flame ionization detectors (FID) and a thermal conductivity detector (TCD), together with an Agilent 6890 with sulfur chemiluminescence dual plasma detector (SCD) is presented. A two-dimensional GC system with Deans switch (heart-cut) and two capillary columns (HP-FFAP and HP-Al2O3) was used for analysis of the organic products on the FIDs. Light inorganic gases (H2, CO, CO2, N2) and methane were separated on packed columns and quantified with the TCD. The "sulfur GC" was optimized for on-line trace level sulfur analysis in hydrocarbon matrices and used to understand to which degree sulfur is released from the catalyst and incorporated into the liquid product, and if so in which form. The method provides excellent quantitative measurements with a carbon material balance near 99.5% (carbon in/carbon out) for individual measurement points.


Subject(s)
Alcohols/chemistry , Chromatography, Gas/instrumentation , Chromatography, Gas/methods , Alcohols/chemical synthesis , Catalysis , Equipment Design , Gases/analysis , Gases/isolation & purification , Hydrocarbons/analysis , Hydrocarbons/isolation & purification , Sulfur Compounds/chemistry
3.
Langmuir ; 28(22): 8479-85, 2012 Jun 05.
Article in English | MEDLINE | ID: mdl-22578053

ABSTRACT

Magnetic iron oxide nanoparticles (MION) for protein binding and separation were obtained from water-in-oil (w/o) and oil-in-water (o/w) microemulsions. Characterization of the prepared nanoparticles have been performed by TEM, XRD, SQUID magnetometry, and BET. Microemulsion-prepared magnetic iron oxide nanoparticles (ME-MION) with sizes ranging from 2 to 10 nm were obtained. Study on the magnetic properties at 300 K shows a large increase of the magnetization ~35 emu/g for w/o-ME-MION with superparamagnetic behavior and nanoscale dimensions in comparison with o/w-ME-MION (10 emu/g) due to larger particle size and anisotropic property. Moringa oleifera coagulation protein (MOCP) bound w/o- and o/w-ME-MION showed an enhanced performance in terms of coagulation activity. A significant interaction between the magnetic nanoparticles and the protein can be described by changes in fluorescence emission spectra. Adsorbed protein from MOCP is still retaining its functionality even after binding to the nanoparticles, thus implying the extension of this technique for various applications.


Subject(s)
Ferric Compounds/chemistry , Magnetite Nanoparticles/chemistry , Moringa oleifera/chemistry , Plant Proteins/chemistry , Seeds/chemistry , Adsorption , Aluminum Silicates/chemistry , Clay , Emulsions , Magnetite Nanoparticles/ultrastructure , Magnetometry , Microscopy, Electron, Transmission , Particle Size , Protein Binding , Spectrometry, Fluorescence , Water , X-Ray Diffraction
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