On viscous flow and azimuthal anisotropy of quark-gluon plasma in strong magnetic field

We calculate the viscous pressure tensor of the quark-gluon plasma in strong magnetic field. It is azimuthally anisotropic and is characterized by five shear viscosity coefficients, four of which vanish when the field strength eB is much larger than the plasma temperature squared. We argue, that the azimuthally anisotropic viscous pressure tensor generates the transverse flow with asymmetry as large as 1/3, even not taking into account the collision geometry. We conclude, that the magnitude of the shear viscosity extracted from the experimental data ignoring the magnetic field must be underestimated.Comment: 10 page

Structural Studies on a Mitochondrial Glyoxalase II

Glyoxalase 2 is a β-lactamase fold-containing enzyme that appears to be involved with cellular chemical detoxification. Although the cytoplasmic isozyme has been characterized from several organisms, essentially nothing is known about the mitochondrial proteins. As a first step in understanding the structure and function of mitochondrial glyoxalase 2 enzymes, a mitochondrial isozyme (GLX2-5) from Arabidopsis thaliana was cloned, overexpressed, purified, and characterized using metal analyses, EPR and 1H NMR spectroscopies, and x-ray crystallography. The recombinant enzyme was shown to bind 1.04 ± 0.15 eq of iron and 1.31 ± 0.05 eq of Zn(II) and to exhibit kcat and Km values of 129 ± 10 s-1 and 391 ± 48 μm, respectively, when using S-d-lactoylglutathione as the substrate. EPR spectra revealed that recombinant GLX2-5 contains multiple metal centers, including a predominant Fe(III)Z-n(II) center and an anti-ferromagnetically coupled Fe(III)Fe(II) center. Unlike cytosolic glyoxalase 2 from A. thaliana, GLX2-5 does not appear to specifically bind manganese. 1H NMR spectra revealed the presence of at least eight paramagnetically shifted resonances that arise from protons in close proximity to a Fe(III)Fe(II) center. Five of these resonances arose from solvent-exchangeable protons, and four of these have been assigned to NH protons on metal-bound histidines. A 1.74-Å resolution crystal structure of the enzyme revealed that although GLX2-5 shares a number of structural features with human GLX2, several important differences exist. These data demonstrate that mitochondrial glyoxalase 2 can accommodate a number of different metal centers and that the predominant metal center is Fe(III)Zn(II)

Neutron Diffraction Studies of ErNi₅₋ₓCoₓ (X=0.68, 1.68, 2.26) Alloys

ErNi5-xCox alloys were prepared by RF induction melting and analyzed using neutron powder diffraction. Rietveld analysis neutron diffraction data indicates the unit cell volume increases with Co content while the a and c lattice parameters show different dependencies on the composition. the Co atoms show higher affinity for the 3g sites than for the 2c sites. the Co sublattice tends to couple antiferromagnetically to the Er sublattice. the easy magnetization direction is along the c axis

Site Affinity of Substituents in Nd₂Fe₁₇₋ₓTₓ (T=Cu,Zr,Nb,Ti,V) Alloys

In order to understand the magnetic properties of the substituted rare-earth-iron alloys, it is especially important to know the location of the substitutional atoms within the iron lattice. The site distributions of some nontransition-metal substituents in the substituted Nd2Fe17-xTx alloys have previously been reported. Here we report the site distributions of some transition-metal substituents (Cu,Zr,Nb,Ti,V) in the Nd2Fe17-xTx alloys and compare them with those of the nontransition-metal substituted compounds. Rietveld analysis of neutron powder diffraction data indicates that the nontransition-metal substituents show very similar site affinity at low substituent content. For example Al, Ga, and Si all prefer the 18h sites. The transition-metal substituents show a more complex site affinity. Ti and V atoms strongly prefer the 6c sites, Cu atoms prefer the 9d and 18f sites, Nb atoms prefer the 6c and 18h sites, and Zr atoms prefer 6c and 18f sites. It was also noted that the site affinity can change if carbon is included in the melting procedure of the sample preparation. The superconducting quantum interference device measurements show that all the substituted compounds have a Curie temperature higher than the unsubstituted parent compound. The relationship between the site distribution of substituents and the magnetic properties of the substituted Nd2Fe17-xTx alloys is discussed

The Relationship Between Magnetic Interactions and Near Neighbor Interatomic Distances in the Transition Metal Sublattice of R(Mn/Fe)6A6 (R=Nd or Sm, A=Ge or Sn)

The magnetic and crystallographic structures of R(Fe/Mn)6A6 (R=Nd or Sm and A=Ge or Sn) intermetallics have been investigated using x-ray and neutron diffraction techniques and superconducting quantum interference device magnetic measurements. For both stannides (A=Sn) and germanides (A=Ge), the lattice contracts with increasing iron content. In the case of the stannides, substitution of manganese by iron enhances the saturation magnetization and Curie temperature at low iron concentrations (x≤2) suggesting the presence of an extremely rare occurrence, positive coupling between iron and manganese magnetic moments. In contrast, the magnetic properties of the germanides deteriorate rapidly as manganese is replaced by iron. This difference in the dependence of magnetic properties on the iron content between the germanides and stannides is explained using the Bethe–Slater relationship between near neighbor exchange interactions and interatomic distances. Based on the observations described in this article, it is concluded that the critical near neighbor interatomic distance above which manganese/iron moments couple positively in these intermetallics is ∼2.614 Å

The Relationship Between Magnetic Interactions and Near Neighbor Interatomic Distances in the Transition Metal Sublattice of R(Mn/Fe)₆A₆(R=Nd or Sm, A=Ge or Sn)

The magnetic and crystallographic structures of R(Fe/Mn)6A6 (R=Nd or Sm and A = Ge or Sn) intermetallics have been investigated using x-ray and neutron diffraction techniques and superconducting quantum interference device magnetic measurements. For both stannides (A = Sn) and germanides (A = Ge), the lattice contracts with increasing iron content. In the case of the stannides, substitution of manganese by iron enhances the saturation magnetization and Curie temperature at low iron concentrations (x ≤2 ) suggesting the presence of an extremely rare occurrence, positive coupling between iron and manganese magnetic moments. In contrast, the magnetic properties of the germanides deteriorate rapidly as manganese is replaced by iron. This difference in the dependence of magnetic properties on the iron content between the germanides and stannides is explained using the Bethe-Slater relationship between near neighbor exchange interactions and interatomic distances. Based on the observations described in this article, it is concluded that the critical near neighbor interatomic distance above which manganese/iron moments couple positively in these intermetallics is ∼2.614 Å.

Neodymium and Erbium Coordination Environments in Phosphate Glasses

The local structures of Nd3+ and Er3+ ions in two series of rare-earth (RE) phosphate glasses with nominal compositions xR203-(1-x)P2O5, where R=Nd and Er and 0.05≤x≤0.28, have been characterized by LIII-edge extended x-ray-absorption fine-structure spectroscopy (EXAFS). The RE coordination number depends on the R2O3 content, decreasing from 9.0 (10) oxygen nearest neighbors in ultraphosphate compositions (x\u3c0.15) to 6.4 (9) oxygen nearest neighbors for the metaphosphate (x∼0.25) compositions. The average Er-O bond distance decreases from 2.29 (1) to 2.23 (1) Å, and the average Nd-O bond distance decreases from 2.40 (1) to 2.37 (1) Å over the same compositional range. The changes in coordination environments are consistent with the conversion of isolated RE polyhedra to clustered RE polyhedra sharing common oxygens as the number of available terminal oxygens per RE ion decreases with increasing x

An Analysis of Iron-Iron Interatomic Distances in Several Rare Earth Transition Metal Intermetallics

As a part of a systematic study of the dependence of iron-iron exchange interactions on near neighbor iron-iron distances in rare earth transition metal magnetic materials, we have conducted a statistical analysis of interatomic distances in Nd2Fe17, Nd2Fe17N3, and Nd2Fe14B. Results, in general, support the notion that larger near neighbor iron-iron distances promote higher Curie temperatures. In this work, special attention has been paid to the expansion of the Nd2Fe17 lattice due to interstitial nitrogenation and the accompanying increase in the Curie temperature. Within the unit cell, the expansion of the Nd2Fe17 lattice due to nitrogenation is highly nonuniform. When nitrided, the distance between near neighbor 6c iron sites in Nd2Fe17 increases only slightly, by 0.021 Å. However, the distances between other near neighbor iron pairs separated by less than 2.45 Å increases by about 0.04 Å. The nitrogenation of Nd2Fe17 effectively reduces the number of near neighbor iron pain separated by less than 2.45 Å by 92%. However, near neighbor interatomic distances involving the 18h sites are the most affected by nitrogenation. Consequently, the 18h site may play a major role in the enhancement of the Curie temperature due to nitrogenation

The Atomic and Magnetic Structure of NdMn(6−x)FexGe6 Solid Solutions

The magnetic and crystallographic properties of induction-melted NdMn(6−x)FexGe6 intermetallics (x=0, 1.0, and 1.5) in the temperature range of 30–475 K have been studied by x-ray and neutron diffraction techniques and SQUID measurements. All of the samples crystallized in the YCo6Ge6-type structure (P6/mmm). A small amount (\u3c5 mol%) of Nd(MnFe)2Ge2 is present as an impurity. As expected, iron replaces manganese at the 3g site. The unit cell volume decreases slightly with increasing iron content at an average rate of 1.3% per substituted atom. Lattice parameters a and c contract at a rate of 0.6% and 0.2% per substitution atom, respectively. The net magnetization of these samples decreases rapidly with increasing iron content. According to neutron diffraction data, the magnetic moment of the iron sublattice couples negatively with ferromagnetically coupled manganese and neodymium moments. Addition of iron suppresses the spin reorientation processes observed in NdMn6Ge6. Whereas the net moment in NdMn5Fe1Ge6 slowly cants away from the c-axis with increasing temperature, the easy direction of NdMn4.5Fe1.5Ge6 is approximately parallel to the c-axis in the temperature range mentioned above