Application of Laser Dispersion Method in Apparatus Combining H Atom Rydberg Tagging Time-of-Flight Technique with Vacuum Ultraviolet Free Electron Laser

Photodissociation of H2S in the VUV region plays an important role in the atmospheric chemistry and interstellar chemistry.To date,however,few studies have been focused on this topic.In this article,we have described a laser dispersion method applied in the apparatus combining the high-n H atom Rydberg tagging time-of-flight technique with the vacuum ultraviolet free electron laser(VUV FEL).The Lyman-αlaser beam(121.6 nm)used in the H-atom detection was generated by the difference frequency four-wave mixing schemes in a Kr/Ar gas cell.After passing through an off-axis biconvex LiF lens,the 121.6 nm beam was dispersed from the 212.6 nm and 845 nm beams due to the different deflection angles experienced by these laser beams at the surfaces of the biconvex lens.This method can eliminate the background signal from the 212.6 nm photolysis.Combined with the VUV FEL,photodissociation of H2S at 122.95 nm was studied successfully.The TOF spectrum was measured and the derived total kinetic energy release spectrum was displayed.The results suggest that the experimental setup is a powerful tool for investigating photodissociation dynamics of molecules in the VUV region which involves the H-atom elimination processes.

Quality control for bloom casting of YQ450NQR1 steel

To reduce surface depression of a bloom, the primary cooling intensity was decreased, and the water distribution of mold wide and narrow faces was optimized. The length of secondary cooling zones and the specific water flow were increased, and the water flow distribution among the secondary cooling zones was adjusted to eliminate central defects, such as center looseness, central segregation, and center line cracks. The operation showed that the proportion of surface depression decreased from 37.22% to 2.87%, whereas the proportion of center looseness for 〈1.0 increased from 79.71% to 90.70%, the proportion of central segregation for 〈0.5 increased from 1.45% to 44.19%, and the proportion of center line cracks that are free increased from 39.13% to 62.79%. The qualified blooms are delivered to produce 310 Z-beam, whose yield strength is greater than 450 MPa.

Ultrafast Decay Dynamics of 2-Hydroxypyridine Excited to S_(1) Electronic State

The S_(1) state decay dynamics of 2-hydroxypyridine following UV excitation at a wavelength range of 276.9-250.0 nm is investigated using femtosecond time-resolved photoelectron imaging technique.Based on pump wavelength dependence of the decay dynamics,a refined decay picture is proposed.At pump wavelength of 276.9 nm,the S_(1) state is depopulated through intersystem crossing to lower triplet state(s).At 264.0 nm,both intersystem crossing to lower triplet state(s)and internal conversion to the ground state are in operation.At 250.0 nm,internal conversion to the ground state becomes dominated.

Crossed Beam Study on the F+D2→DF+D Reaction at Hyperthermal Collision Energy of 23.84 kJ/mol

We presented an experimental apparatus combining the H-atom Rydberg tagging time-of-flight technique and the laser detonation source for studying crossed beam reactions at hyperthermal collision energies. The preliminary study of the F+D2→DF+D reaction at hyperthermal collision energy of 23.84 kJ/mol was performed. Two beam sources were used in this study: one is the hyperthermal F beam source produced by a laser detonation process, and the other is D2 beam source generated by liquid-N2 cooled pulsed valve. Vibrational state-resolved di erential cross sections (DCSs) of product for the title reaction were determined. From the product vibrational state-resolved DCS, it can be concluded that products DF(v'=0, 1, 2, 3) are predominantly distributed in the sideway and backward scattering directions at this collision energy. However, the highest vibrational excited product DF(v'=4), is clearly peaked in the forward direction. The probable dynamical origins for these forward scattering products were analyzed and discussed.

Ultrafast Decay Dynamics of N-Ethylpyrrole Excited to the S_(1)Electronic State:A Femtosecond Time-Resolved Photoelectron Imaging Study

N-ethylpyrrole is one of ethylsubstituted derivatives of pyrrole and its excited-state decay dynamics has never been explored.In this work,we investigate ultrafast decay dynamics of N-ethylpyrrole excited to the S_(1)electronic state using a femtosecond time-resolved photoelectron imaging method.Two pump wavelengths of 241.9 and 237.7 nm are employed.At 241.9 nm,three time constants,5.0±0.7 ps,66.4±15.6 ps and 1.3±0.1 ns,are derived.For 237.7 nm,two time constants of 2.1±0.1 ps and 13.1±1.2 ps are derived.We assign all these time constants to be associated with different vibrational states in the S_(1)state.The possible decay mechanisms of different S_(1)vibrational states are briefly discussed.

Ultrafast Dynamics of Water Molecules Excited to Electronic ■ States:A Time-Resolved Photoelectron Spectroscopy Study

The ultrafast dynamics of water molecules excited to the two F states is studied by combining two-photon excitation and time-resolved photoelectron imaging techniques. The lifetimes of the F1A1 and F1B1 states of H2O (D2O) were derived to be 1.0±0.3 (1.9±0.4) and 10±3 (30±10) ps, respectively. We propose that the F1A1 state mainly decays through the D state, due to the nonadiabatic coupling between them, while the F1B1 state decays through the F1A1 state via Coriolis interaction.

Ultraviolet Photodissociation Dynamics of DNCO+hν→D+NCO: Two Competitive Pathways

Photodissociation dynamics of DNCO+hv→D+NCO at photolysis wavelengths between 200 and 235 nm have been studied using the D-atom Rydberg tagging time-of-flight technique. Product translational energy distributions and angular distributions have been determined. Nearly statistical distribution of the product translational energy with nearly isotropic angular distribution was observed at 210-235 nm, which may come from the predissociation pathway of internal conversion from S1 to S0 state followed by decomposition on S0 surface. At shorter photolysis wavelengths, in addition to the statistical distribution, another feature with anisotropic angular distribution appears at high translational energy region, which can be attributed to direct dissociation on S1 surface. Compared with HNCO, the direct dissociation pathway for DNCO photodissociation opens at higher excitation energy. According to our assignment of the NCO internal energy distribution, dominantly bending and a little stretching excited NCO was produced via both dissociation pathways.

Analysis on the therapeutic effects of integrated traditional Chinese and Western medicine on ulcerative colitis and its effects on coagulation function and inflammatory factors

Objective:To analyze the therapeutic effects of Integrated Traditional Chinese and Western Medicine on ulcerative colitis (UC) and its effects on coagulation function and inflammatory factors.Methods: 220 cases of patients with UC were selected as the research subjects and randomly divided into the observation group and the control group, 110 cases were included into each group. The patients in the control group were treated with single western medicine, while the patients in the observation group were treated with enema treatment of traditional Chinese Medicine. The clinical therapeutic effects of the two groups were evaluated and compared. The blood coagulation indexes of the activated partial thromboplastin time (APTT), prothrombin time (PT), the plasma fibrinogen (Fib), the D dimer (D-D) of two groups patients who in the treatment were detected and compared. The serum tumor necrosis factor (TNF-α), interleukin-6 (IL-6), interleukin-8 (IL-8) levels of the patients in the two groups were measured and compared.Results: The clinical efficiencies of the observation group and the control group were 97% and 75%, the clinical efficiencies and the therapeutic effects of the observation group were better than those in the control group, there were statistically significant differences between the two groups. The plasma Fib levels and the plasma D-D levels after the treatment of the patients in the two groups were significantly lower than those before the treatment, the difference was statistically significant. The plasma Fib levels and the plasma D-D levels after the treatment of the patients in the observation group were lower than those in the control group, the difference was statistically significant. The serum inflammatory factors levels after the treatment of the patients in the two groups were significantly lower than those before the treatment, the difference was statistically significant. The serum inflammatory factors levels after the treatment of the patients in the observation group were lower than those in the control group, the difference is powerful and have statistically significant.Conclusion: The application of Integrated Traditional Chinese and Western Medicine in the treatment of UC can improve the therapeutic effect significantly, correct imbalance of the patients' coagulation dissolution function, reduce the degree of inflammatory reaction, which benefits to promote of the patients' rehabilitation, reduce the incidence of complications and improve the prognosis of patients.

Nanopore-Based Metal Ion Detection and Metal Ion-Mediated Nanopore Sensing

With the continuous development of nanotechnology,single-molecule nanopore detection has become a popular research topic.In this review,we summarize the application of biological nanopores for metal ions detection as well as overview the function of metal ions in the ion-mediated nanopore detection of different analytes in recent decades.According to the previous reports,biological nanopores utilize two strategies to detect metal ions.First,the specific binding sites are engineered in the nanopore to slow down the translocation rate of metal ions,resulting in the diverse specific current blockage signals.Secondly,the external molecule probes are added in the detection system to interact with metal ions,leading to the characteristic changes in the signals.At the same time,the external addition of metal ions into the nanopore detection systems enhances the sensitivity and selectivity through the changes of pore charges,the coordination with analytes or indirect detection.This review provides a summary on the role of metal ions in the application of nanopore detection technology.