Salt System (salt + system)

Distribution by Scientific Domains


Selected Abstracts


Partitioning and Characterization of Tyrosine-Tagged Green Fluorescent Proteins in Aqueous Two-Phase Systems

BIOTECHNOLOGY PROGRESS, Issue 3 2004
Sara Fexby
The green fluorescent protein GFPuv has been genetically engineered to investigate the influence of N-terminal tyrosine extensions in aqueous two-phase systems. Fusions in the N-terminus affected the protein expression, and tags containing three tyrosines and prolines influenced the expression favorably. This effect is probably due to changes in mRNA stability, because the amounts of corresponding mRNAs correlated with the amounts of GFPuv proteins. The partitioning was investigated in two different aqueous two-phase systems, a two-polymer system composed of EO30PO70/dextran and a PEG/salt system with potassium phosphate. Partitioning in the PEG/salt system generally was more favorable than in the EO30PO70/dextran system. Tags with three tyrosines resulted in higher partitioning toward the EO30PO70- and PEG-rich phases, respectively. The effect of adding proline residues to the tag was also investigated, and the partitioning effect of the tag was enhanced when prolines were included in the tags with three tyrosines. The best tyrosine tag, Y3P2, increased the partition coefficient 5 times in the PEG/salt system. Thermoseparation of the EO30PO70 phase allowed recovery of 83% Y3P2-GFPuv protein in a water phase. [source]


ChemInform Abstract: Amination Reactions of Aryl Halides with Nitrogen-Containing Reagents Mediated by Palladium/Imidazolium Salt Systems.

CHEMINFORM, Issue 18 2002
Gabriela A. Grasa
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


Dynamic modelling of passive margin salt tectonics: effects of water loading, sediment properties and sedimentation patterns

BASIN RESEARCH, Issue 3 2005
Lykke Gemmer
We investigate the evolution of passive continental margin sedimentary basins that contain salt through two-dimensional (2D) analytical failure analysis and plane-strain finite-element modelling. We expand an earlier analytical failure analysis of a sedimentary basin/salt system at a passive continental margin to include the effects of submarine water loading and pore fluid pressure. Seaward thinning sediments above a weak salt layer produce a pressure gradient that induces Poiseuille flow in the viscous salt. We determine the circumstances under which failure at the head and toe of the frictional,plastic sediment wedge occurs, resulting in translation of the wedge, landward extension and seaward contraction, accompanied by Couette flow in the underlying salt. The effects of water: (i) increase solid and fluid pressures in the sediments; (ii) reduce the head to toe differential pressure in the salt and (iii) act as a buttress to oppose failure and translation of the sediment wedge. The magnitude of the translation velocity upon failure is reduced by the effects of water. The subsequent deformation is investigated using a 2D finite-element model that includes the effects of the submarine setting and hydrostatic pore pressures. The model quantitatively simulates a 2D approximation of the evolution of natural sedimentary basins on continental margins that are formed above salt. Sediment progradation above a viscous salt layer results in formation of landward extensional basins and listric normal growth faults as well as seaward contraction. At a later stage, an allochthonous salt nappe overthrusts the autochthonous limit of the salt. The nature and distribution of major structures depends on the sediment properties and the sedimentation pattern. Strain weakening of sediment favours landward listric growth faults with formation of asymmetric extensional depocentres. Episodes of low sediment influx, with partial infill of depocentres, produce local pressure gradients in the salt that result in diapirism. Diapirs grow passively during sediment aggradation. [source]


A new method of potassium chromate production from chromite and KOH-KNO3 -H2O binary submolten salt system

AICHE JOURNAL, Issue 10 2009
Zhi Sun
Abstract A new method of chromate production by applying a new reaction system of KOH-KNO3 -H2O (binary submolten salt system) is proposed and proved feasible. Under conditions of temperature 350°C, KOH-to-chromite ore ratio 2:1, stirring speed 700 rpm, KNO3 -to-chromite ore ratio 0.8:1, oxygen partial pressure 50%, and gas flow 1 L/min, chromium conversion ratio obtained is >98% with reaction time around 300 min. The decomposition of chromite ore in the system is a typical process of solid, liquid,gas reaction, which is coordinately controlled by mass diffusion in product layer and interface reaction. Apparent activation energy of decomposition in the temperature range from 280 to 370°C is 55.63 kJ/mol. During reaction, oxygen dissolves into KOH-KNO3 -H2O melt system first and some cluster, e.g. O, is formed and the mass diffusion coefficient of the cluster was calculated. The system can be considered as both a media of oxygen transportation and reactant donator. Potassium nitrate plays a role of catalyst in the oxidation decomposition reaction of chromite ore and potassium hydroxide. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source]


Alternating copolymerization of carbon dioxide and epoxide catalyzed by an aluminum Schiff base,ammonium salt system

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 18 2005
Hiroshi Sugimoto
Abstract The alternating copolymerization of carbon dioxide (CO2) and cyclohexene oxide (CHO) with an aluminum Schiff base complex in conjunction with an appropriate additive as a novel initiator is demonstrated. A typical example is the copolymerization of CO2 and CHO with the (Salophen)AlMe (1a),tetraethylammonium acetate (Et4NOAc) system. When a mixture of the 1a,Et4NOAc system and CHO was pressurized by CO2 (50 atm) at 80 °C in CH2Cl2, the copolymerization of CO2 and CHO took place smoothly and produced a high polymer yield in 24 h. From the IR and NMR spectra, the product was characterized to be a copolymer of CO2 and CHO with an almost perfect alternating structure. The matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis indicated that an unfavorable reaction between Et4NOAc and CH2Cl2 and a possible chain-transfer reaction with concomitant water occurred, and this resulted in the bimodal distribution of the obtained copolymer. With carefully predried reagents and apparatus, the alternating copolymerization in toluene gave a copolymer with a unimodal and narrower molecular weight distribution. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4172,4186, 2005 [source]


Hydrophobic interaction chromatography in dual salt system increases protein binding capacity

BIOTECHNOLOGY & BIOENGINEERING, Issue 5 2009
Anna M. Senczuk
Abstract Hydrophobic interaction chromatography (HIC) uses weakly hydrophobic resins and requires a salting-out salt to promote protein,resin interaction. The salting-out effects increase with protein and salt concentration. Dynamic binding capacity (DBC) is dependent on the binding constant, as well as on the flow characteristics during sample loading. DBC increases with the salt concentration but decreases with increasing flow rate. Dynamic and operational binding capacity have a major raw material cost/processing time impact on commercial scale production of monoclonal antibodies. In order to maximize DBC the highest salt concentration without causing precipitation is used. We report here a novel method to maintain protein solubility while increasing the DBC by using a combination of two salting-out salts (referred to as dual salt). In a series of experiments, we explored the dynamic capacity of a HIC resin (TosoBioscience Butyl 650M) with combinations of salts. Using a model antibody, we developed a system allowing us to increase the dynamic capacity up to twofold using the dual salt system over traditional, single salt system. We also investigated the application of this novel approach to several other proteins and salt combinations, and noted a similar protein solubility and DBC increase. The observed increase in DBC in the dual salt system was maintained at different linear flow rates and did not impact selectivity. Biotechnol. Bioeng. 2009;103: 930,935. © 2009 Wiley Periodicals, Inc. [source]