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11.
Phillips John R. Clausen Edgar C. Gaddy James L. 《Applied biochemistry and biotechnology》1994,45(1):145-157
Synthesis gas provides a simple substrate for the production of fuels and chemicals. Synthesis gas can be produced via established technologies from a variety of feedstocks including coal, wood, and agricultural and municipal wastes. The gasification is thermally efficient and results in complete conversion of the feedstock to fermentable substrate.Clostridium ljungdahlii grows on the synthesis gas components, carbon monoxide, hydrogen, and carbon dioxide. Production of acetic acid and ethanol accompanies growth with synthesis gas as sole source of energy and carbon. Rate and yield parameters are compared forC. ljungdahlii grown on carbon monoxide, or hydrogen with carbon dioxide.
相似文献12.
A micromethod for the determination of ascorbic acid has been developed. A 2–10 mg sample dissolved in glacial acetic acid is reacted with a known excess of bromine monochloride at ice-bath temperature, and the excess reagent is back-titrated iodometrically. The maximum deviation in the results is ± 1.5%. 相似文献
13.
Kristian Syberg Maria Bille Nielsen Lauge Peter Westergaard Clausen Geert van Calster Annemarie van Wezel Chelsea Rochman Albert A. Koelmans Richard Cronin Sabine Pahl Steffen Foss Hansen 《Current Opinion in Green and Sustainable Chemistry》2021
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14.
Methane production from synthesis gas using a mixed culture ofR. rubrum M. barkeri,and M. formicicum
Klasson K. T. Cowger J. P. Ko C. W. Vega J. L. Clausen E. C. Gaddy J. L. 《Applied biochemistry and biotechnology》1990,(1):317-328
The components of synthesis gas, CO, H2, and CO2, may be converted into CH4 biologically through either acetate or H2/CO2 as intermediates. Of these two routes, conversion through H2/CO2 is preferred. This paper presents results of mixed-culture studies employing the photosynthetic bacteriumR. rubrum for converting CO to CO2 and H2 by the water gas shift reaction and two methanogens,M. formicicum andM. barkeri, for converting CO2 and H2 into CH4. Results are presented for triculture operation in two types of reactors, the packed bubble column and the trickle-bed reactor. 相似文献
15.
16.
O. Elsenhans P. Fischer A. Furrer K. N. Clausen H. G. Purwins F. Hulliger 《Zeitschrift für Physik B Condensed Matter》1991,82(1):61-75
Compared to previous bulk magnetic measurements unusual magnetic ordering phenomena were detected by systematic neutron scattering experiments performed in the temperature range of 7 mKT300 K on the series of cubic metallic compounds REPd3 of the rare earths RE=Nd, Tb, Dy, Er, Tm and Yb. Except for ErPd3 withT
N
=3 K the observed critical temperatures are compatible with the de Gennes scaling. The complexity of long-range magnetic ordering increases with decreasing 4f
n
occupancy, ranging from ferro- or ferrimagnetism in YbPd3 and DyPd3 via commensurate antiferromagnetic ordering in ErPd3 and TmPd3 [k=(1/2, 1/2, 0)] to incommensurate antiferromagnetic ordering of modulated type in TbPd3 and NdPd3. Both RKKY interactions, crystalline electric field, hybridization with 4d states of Pd as well as nuclear spin polarization in the case of RE=Nd appear to be of importance for the magnetic properties of REPd3 systems. 相似文献
17.
18.
Citric acid is finding new areas of use each year and the demand for the acid is constantly increasing. Being a bulk chemical,
the continuous production of citric acid would be advantageous. The paper presents the results from ammonia limited batch
and continuous fermentations using the yeast strainSaccharomycopsis (Candida) lipolytica (NRRL Y-7576). Mathematical models were developed for growth and glucose utilization in batch and continuous culture. Cell
and acid yields appeared to be almost the same in batch and continuous culture. The specific production rates were found to
be constant, equal to 0.053 g/g h, in the batch fermentations but varied in the continuous experiments from 0 to 0.11 g/g
h depending on the fermentation conditions. Continuous production in a single stage CSTR was studied for over 1,000 hours
without shutdown. 相似文献
19.
Gryko DT Clausen C Roth KM Dontha N Bocian DF Kuhr WG Lindsey JS 《The Journal of organic chemistry》2000,65(22):7345-7355
The attachment of redox-active molecules such as porphyrins to an electroactive surface provides an attractive approach for electrically addressable molecular-based information storage. Porphyrins are readily attached to a gold surface via thiol linkers. The rate of electron transfer between the electroactive surface and the porphyrin is one of the key factors that dictates suitability for molecular-based memory storage. This rate depends on the type and length of the linker connecting the thiol unit to the porphyrin. We have developed different routes for the preparation of thiol-derivatized porphyrins with eight different linkers. Two sets of linkers explore the effects of linker length and conjugation, with one set comprising phenylethyne units and one set comprising alkyl units. One electron-deficient linker has four fluorine atoms attached directly to a thiophenyl unit. To facilitate the synthesis of the porphyrins, convenient routes have been developed to a wide range of aldehydes possessing a protected S-acetylthio group. An efficient synthesis of 1-(S-acetylthio)-4-iodobenzene also has been developed. A set of porphyrins, each bearing one S-acetyl-derivatized linker at one meso position and mesityl moieties at the three remaining meso positions, has been synthesized. Altogether seven new aldehydes, eight free base porphyrins and eight zinc porphyrins have been prepared. The zinc porphyrins bearing the different linkers all form self-assembled monolayers (SAMs) on gold via in situ cleavage of the S-acetyl protecting group. The SAM of each porphyrin is electrochemically robust and exhibits two reversible oxidation waves. 相似文献
20.
The adsorption of cationic and amphoteric copolymers onto controlled pore glass (CPG) powders has been studied by measurement of the powder particle zeta (zeta) potential, by determination of the adsorption isotherm, and by FT Raman measurements of the polymer-coated powder. The cationic polymers consisted chiefly of homopolymers of dimethyldiallylammonium chloride (DMDAAC) or copolymers of DMDAAC and acrylamide. The amphoteric polymers studied included copolymers of DMDAAC and acrylic acid. The comonomer ratio was varied to explore the dependence of cationic charge density on the extent and effect of adsorption. Both types of polymers adsorb onto the anionic glass surface via an ion-exchange mechanism. Consequently, a correspondingly higher mass of a low-charge-density copolymer adsorbs than of a cationic homopolymer. The presence of the anionic portion in the amphoteric polymers does not significantly alter this picture. The zeta potential, however, reflects the overall nature of the polymer. Cationic polymers effectively neutralize the glass surface, while amphoteric polymers leave the zeta potential net negative. Adsorption isotherms, determined via the depletion technique using colloidal titration, were used to "calibrate" a FT Raman method. The latter was used to determined the amount of adsorbed polymer under solution conditions in which colloidal titration could not be performed. 相似文献