Effect of high magnetic fields on the martensite transformation

The effect of high magnetic fields up to 132 kOe on the martensite transformation has been investigated in two alloy steels, 52100 bearing steel and a type 410 stainless steel. In both cases the martensite start temperature is raised by the application of a magnetic field, and the increase inM _s is linear with field. The rate of formation of martensite is not affected by the field. Numerical values for the entropy of the austenite-martensite reaction can be obtained from the experimental results, and are in reasonable agreement with previous results and with theoretical calculations.     

Effect of high magnetic fields on the martensite transformation

The effect of high magnetic fields up to 132 kOe on the martensite transformation has been investigated in two alloy steels, 52100 bearing steel and a type 410 stainless steel. In both cases the martensite start temperature is raised by the application of a magnetic field, and the increase inM _s is linear with field. The rate of formation of martensite is not affected by the field. Numerical values for the entropy of the austenite-martensite reaction can be obtained from the experimental results, and are in reasonable agreement with previous results and with theoretical calculations. Richard Fields was formerly a student.     

Evidence of morphological and physiological transformation of mammalian cells by strong magnetic fields

Cultures of L-929 and WI-38 cells, frozen to 4.2 degrees K and exposed for 4 to 8 hours to 5000-oersted magnetic fields, were markedly inhibited in their growth as compared to controls. In cultures grown on cover slips, approximately 7 days after exposure, morphologically distinct cells emerged and were propagated from generation to generation; 3 weeks later, in flask cultures, contact inhibition was abolished. It is concluded that under certain experimental conditions, strong magnetic fields induce morphological and physiological transformations of target cells.     

Dissolution of thrombotic arterial occlusion by high intensity, low frequency ultrasound and dodecafluoropentane emulsion: an in vitro and in vivo study

OBJECTIVES: We examined the effectiveness of the microbubbles of an echo contrast agent, dodecafluoropentane (DDFP) emulsion, to enhance low frequency ultrasound clot disruption in vitro and in vivo. BACKGROUND: Ultrasound is reported to facilitate clot dissolution, and microbubbles could theoretically enhance ultrasound clot dissolution by augmenting cavitational effects. METHODS: In vitro studies: The disruption rate of fresh human clots by ultrasound (24 kHz, 2.9 W/cm2) was examined in saline and DDFP emulsion. In vivo studies: Using a rabbit iliofemoral thrombotic occlusion model, recanalization rate and histopathologic findings were compared among groups treated with DDFP emulsion alone, transcutaneous ultrasound (20 kHz, 1.5 W/cm2) alone and with DDFP emulsion and ultrasound combined. RESULTS: The ultrasound clot disruption rate was significantly (p < 0.01) increased, from 72 +/- 18% (mean +/- SD) in saline to 98 +/- 4% in DDFP emulsion in 3 min in vitro. No vessel was recanalized by DDFP emulsion alone (0%), and only a single artery was patent after ultrasound treatment alone (9%). In contrast, 82% of iliofemoral arteries were angiographically recanalized after ultrasound treatment with DDFP emulsion. Histologically, the patent arteries had only minimal focal mural thrombus, with no evidence of vessel wall damage. However, substantial damage was observed in rabbit dermis and subcutaneous tissue. CONCLUSIONS: 1) DDFP emulsion, an echo contrast agent, significantly enhances the clot-disrupting effect of low frequency ultrasound in vitro and in an in vivo rabbit iliofemoral occlusion model. 2) This simple combination therapy has potential for clinical application in patients with thrombotic arterial occlusions.     

氧化矿强精单独选别工艺流程的试验研究

针对氧化矿强磁精矿、弱磁精矿两种不同矿物采用单独反浮选工艺流程进行工业试验与研究,指出强精单独反浮选试验为下一步正浮选提供可靠的依据,达到氧化矿提质降杂的目的.     

Effect of mimosine on DNA synthesis in mammalian cells

We have designed a general protocol to assess the rate of replicon initiation in mammalian cells in the presence of inhibitors of DNA synthesis. It is based on cross-linking DNA in vivo with trioxsalen, which effectively blocks the movement of the replication forks along DNA, while having little effect on initiation of replication. We applied this protocol to study the effect of the plant amino acid mimosine on the rate of replicon initiation in exponentially growing murine erythroleukemia F4N cells. We found out that during the first 2 h after application of 25-400 microM mimosine, the initiation step was inhibited more efficiently than the overall DNA synthesis. In this respect, the effect of mimosine was similar to that of gamma-ray irradiation and differed from that of hydroxyurea and aphidicolin. The results suggest that in addition to inhibiting the elongation step of DNA synthesis, mimosine inhibits the initiation of DNA replication as well.