Light anti-nuclei production in pp collisions at s\sqrt{s}=7 and 14 TeV

A dynamically constrained coalescence model based on the phase space quantization and classical limit method was proposed to investigate the production of light nuclei (anti-nuclei) in non-single diffractive (NSD) pp collisions at $\sqrt{s}$=7 and 14 TeV. This calculation was based on the final hadronic state in the PYTHIA and PACIAE model simulations, the event sample consisted of 1.2$\times 10^8$ events in both simulations. The PACIAE model calculated $\bar D$ yield of 6.247$\times 10^{-5}$ in NSD pp collisions at $\sqrt{s}$=7 TeV is well comparing with the ALICE rough datum of 5.456$\times 10^{-5}$. It indicated the reliability of proposed method in some extent. The yield, transverse momentum distribution, and rapidity distribution of the $\bar D$, $^3{\bar{He}}$, and $_{\bar\Lambda} ^3{\bar H}$ in NSD pp collisions at $\sqrt{s}$=7 and 14 TeV were predicted by PACIAE and PYTHIA model simulations. The yield resulted from PACIAE model simulations is larger than the one from PYTHIA model. This might reflect the role played by the parton and hadron rescatterings.Comment: 5 pages, 2 figure

Quantum generalized Reed-Solomon codes: Unified framework for quantum MDS codes

We construct a new family of quantum MDS codes from classical generalized Reed-Solomon codes and derive the necessary and sufficient condition under which these quantum codes exist. We also give code bounds and show how to construct them analytically. We find that existing quantum MDS codes can be unified under these codes in the sense that when a quantum MDS code exists, then a quantum code of this type with the same parameters also exists. Thus as far as is known at present, they are the most important family of quantum MDS codes.Comment: 9 pages, no figure

(3S,12R,20S,24R)-20,24-Ep­oxy­dammarane-3,12,25-triol

In the title mol­ecule, C30H52O4, the three six-membered rings are in chair conformations, the cyclo­pentane ring is in an envelope form and the tetra­hydro­furan ring has a conformation inter­mediate between half-chair and sofa. In the crystal, mol­ecules are linked by inter­molecular O—H⋯O hydrogen bonds into helical chains along [100]. Two intra­molecular O—H⋯O hydrogen bonds are also present. One C atom of the tetrahydrofuran ring and its attached H atoms are equally disordered over two sets of sites

Fenton Reagent Oxidation and Decolorizing Reaction Kinetics of Reactive Red SBE

AbstractFenton reagent was employed to treat and decolorize the wastewater of Reactive Red SBE by on-line spectrophotometry. The effects of initial FeSO4 concentration, initial H2O2 concentration, pH, reactive red SBE and temperature on the decoloration of reactive red SBE were investigated. The results show that Fenton oxidize process follows pseudo first order kinetics in the first stage and reaction activation energy is 2.608 kJ/mol. The decolorizing reaction rate constants (k) increase with the rise of FeSO4 concentration, H2O2 concentration, temperature, but decrease with the rise of reactive red SBE, and the optimum pH is 3. Initial FeSO4 concentration and initial H2O2 concentration against k are linear correlation