Reduction and Analysis of Low Temperature Shift Heterogeneous Catalyst for Water Gas Reaction in Ammonia Production

Radi dobivanja dodatnih količina vodika nakon reakcija parnog reformiranja prirodnog plina te zaštite rada heterogenog katalizatora za sintezu amonijaka bitno je postići i održavati maksimalnu aktivnost, selektivnost i stabilnost heterogenog katalizatora niskotemperaturne pretvorbe (konverzije) vodenog plina. Budući da se heterogeni katalizator isporučuje u oksidiranom obliku, presudno je provođenje pravilnog postupka redukcije. Pravilnim postupkom redukcije i kontinuiranom analizom njegova rada osigurava se nužno potrebna aktivnost, selektivnost i stabilnost tijekom primjene. Da bi se uspješno provela redukcija heterogenog katalizatora za niskotemperaturnu pretvorbu vodenog plina, potrebno je osim procesne opreme za provođenje postupka redukcije primjenjivati pouzdan i realan sustav za mjerenje temperature radi učinkovitog uvida u temperaturne profile unutar reaktora pri provedbi egzotermne reakcije kroz sve slojeve heterogenog katalizatora. Kako bi se provjerila učinkovitost redukcije te omogućila analiza njegova rada, potrebno je u pravilnim razdobljima određivati odnos odgovarajućih temperaturnih profila i konstante ravnoteže reakcije. To se postiže analizom temperaturnih profila u pojedinim slojevima heterogenog katalizatora putem "S" i padajućih temperaturnih krivulja. Na temelju dobivenih podataka može se na zadovoljavajući način određivati optimalna temperatura na ulazu u reaktor kako bi se osigurao maksimalni vijek katalizatora. U radu je opisana redukcija heterogenog katalizatora in situ te dan prikaz sustava za praćenje temperature unutar pojedinih slojeva, kako bi se postigao minimalan sadržaj ugljikova (II) oksida na izlazu iz reaktora. Opisani sustav za praćenje temperature kroz slojeve heterogenog katalizatora osigurao je uspješnu redukciju koja se zasnivala na optimalnom povećanju temperature na ulazu u reaktor. Primijenjenim sustavom postignute su zadovoljavajuće katalitičke značajke (aktivnost, selektivnost i stabilnost). Također je omogućeno predviđanje rada katalizatora te donošenje odluke o potrebi njegove zamjene, što izravno utječe na smanjenje troškova proizvodnje.In order to obtain additional quantities of hydrogen after the reforming reactions of natural gas and protect the ammonia synthesis catalyst, it is crucial to achieve and maintain maximum possible activity, selectivity and stability of the low temperature shift catalyst for conversion of water gas reaction during its lifetime. Whereas the heterogeneous catalyst comes in oxidized form, it is of the utmost importance to conduct the reduction procedure properly. The proper reduction procedure and continuous analysis of its performance would ensure the required activity, selectivity and stability throughout the catalyst’s service time. For the proper reduction procedure of the low temperature shift catalyst, in addition to process equipment, also necessary is a reliable and realistic system for temperature measurements, which will be effective for monitoring the exothermal temperature curves through all catalyst bed layers. For efficiency evaluation of low shift temperature catalyst reduction and its optimization, it is necessary to determine at regular time intervals the temperature approach to equilibrium and temperature profiles of individual layers by means of “S” and “die off” temperature exothermal curves. Based on the obtained data, the optimum inlet temperature could be determined, in order to maximally extend the service life of the heterogeneous catalyst as much as possible, and achieve the optimum equilibrium for conversion of the water gas. This paper presents the methodology for in situ reduction of the low temperature shift heterogeneous catalyst and the developed system for monitoring its individual layers to achieve the minimum possible content of carbon monoxide at the exit of the reactor. The developed system for temperature monitoring through heterogeneous catalyst layers provides the proper procedure for reduction and adjustment of optimum process working conditions for the catalyst by the continuous increase of reactor inlet temperature. The applied system provides maximum catalytic activity, selectivity and stability, as well as enables prediction of the catalyst\u27s performance, which can be the basis for a proper decision on its timely replacement, and significant reduction of production costs

Sum rule for the optical scattering rates

An important quantity in electronic systems is the quasiparticle scattering rate (QPSR). A related optical scattering rate (OSR) is routinely extracted from optical data, and, while it is not the same as the QPSR, it nevertheless displays many of the same features. We consider a sum rule which applies to the area under a closely related quantity, almost equal to the OSR in the low energy region. We focus on the readjustment caused by, for example, a quasiparticle density of states change due to the superconducting transition. Unfortunately, no general statement about mechanism can be made solely on the energy scale in which the spectral weight readjustment on the OSR occurs.Comment: 22 pages, 7 figures accepted for publication by Phys. Rev.

Observation of the Cabibbo-suppressed decay Xi_c+ -> p K- pi+

We report the first observation of the Cabibbo-suppressed charm baryon decay Xi_c+ -> p K- pi+. We observe 150 +- 22 events for the signal. The data were accumulated using the SELEX spectrometer during the 1996-1997 fixed target run at Fermilab, chiefly from a 600 GeV/c Sigma- beam. The branching fractions of the decay relative to the Cabibbo-favored Xi_c+ -> Sigma+ K- pi+ and Xi_c+ -> X- pi+ pi+ are measured to be B(Xi_c+ -> p K- pi+)/B(Xi_c+ -> Sigma+ K- pi+) = 0.22 +- 0.06 +- 0.03 and B(Xi_c+ -> p K- pi+)/B(Xi_c+ -> X- pi+ pi+) = 0.20 +- 0.04 +- 0.02, respectively.Comment: 5 pages, RevTeX, 3 figures (postscript), Submitted to Phys. Rev. Let

Transcriptional activity of Hyacinthus orientalis L. female gametophyte cells before and after fertilization

We characterized three phases of Hyacinthus orientalis L. embryo sac development, in which the transcriptional activity of the cells differed using immunolocalization of incorporated 5′-bromouracil, the total RNA polymerase II pool and the hypo- (initiation) and hyperphosphorylated (elongation) forms of RNA Pol II. The first stage, which lasts from the multinuclear stage to cellularization, is a period of high transcriptional activity, probably related to the maturation of female gametophyte cells. The second stage, encompassing the period of embryo sac maturity and the progamic phase, involves the transcriptional silencing of cells that will soon undergo fusion with male gametes. During this period in the hyacinth egg cell, there are almost no newly formed transcripts, and only a small pool of RNA Pol II is present in the nucleus. The transcriptional activity of the central cell is only slightly higher than that observed in the egg cell. The post-fertilization stage is related to the transcriptional activation of the zygote and the primary endosperm cell. The rapid increase in the pool of newly formed transcripts in these cells is accompanied by an increase in the pool of RNA Pol II, and the pattern of enzyme distribution in the zygote nucleus is similar to that observed in the somatic cells of the ovule. Our data, together with the earlier results of Pięciński et al. (2008), indicate post-fertilization synthesis and the maturation of numerous mRNA transcripts, suggesting that fertilization in H. orientalis induces the activation of the zygote and endosperm genomes

A Deubiquitylating Complex Required for Neosynthesis of a Yeast Mitochondrial ATP Synthase Subunit

The ubiquitin system is known to be involved in maintaining the integrity of mitochondria, but little is known about the role of deubiquitylating (DUB) enzymes in such functions. Budding yeast cells deleted for UBP13 and its close homolog UBP9 displayed a high incidence of petite colonies and slow respiratory growth at 37°C. Both Ubp9 and Ubp13 interacted directly with Duf1 (DUB-associated factor 1), a WD40 motif-containing protein. Duf1 activates the DUB activity of recombinant Ubp9 and Ubp13 in vitro and deletion of DUF1 resulted in the same respiratory phenotype as the deletion of both UBP9 and UBP13. We show that the mitochondrial defects of these mutants resulted from a strong decrease at 37°C in the de novo biosynthesis of Atp9, a membrane-bound component of ATP synthase encoded by mitochondrial DNA. The defect appears at the level of ATP9 mRNA translation, while its maturation remained unchanged in the mutants. This study describes a new role of the ubiquitin system in mitochondrial biogenesis

Structure and Mechanism of RNA Polymerase II CTD Phosphatases

Recycling of RNA polymerase II (Pol II) after transcription requires dephosphorylation of the polymerase C-terminal domain (CTD) by the phosphatase Fcp1. We report the X-ray structure of the small CTD phosphatase Scp1, which is homologous to the Fcp1 catalytic domain. The structure shows a core fold and an active center similar to those of phosphotransferases and phosphohydrolases that solely share a DXDX(V/T) signature motif with Fcp1/Scp1. We demonstrate that the first aspartate in the signature motif undergoes metal-assisted phosphorylation during catalysis, resulting in a phosphoaspartate intermediate that was structurally mimicked with the inhibitor beryllofluoride. Specificity may result from CTD binding to a conserved hydrophobic pocket between the active site and an insertion domain that is unique to Fcp1/Scp1. Fcp1 specificity may additionally arise from phosphatase recruitment near the CTD via the Pol II subcomplex Rpb4/7, which is shown to be required for binding of Fcp1 to the polymerase in vitro

A structural perspective of CTD function

The C-terminal domain (CTD) of RNA polymerase II (Pol II) integrates nuclear events by binding proteins involved in mRNA biogenesis. CTD-binding proteins recognize a specific CTD phosphorylation pattern, which changes during the transcription cycle, due to the action of CTD-modifying enzymes. Structural and functional studies of CTD-binding and -modifying proteins now reveal some of the mechanisms underlying CTD function. Proteins recognize CTD phosphorylation patterns either directly, by contacting phosphorylated residues, or indirectly, without contact to the phosphate. The catalytic mechanisms of CTD kinases and phosphatases are known, but the basis for CTD specificity of these enzymes remains to be understood