Non-thermal ablation of expanded polytetrafluoroethylene with an intense femtosecond-pulse laser

Ablation of expanded polytetrafluoroethylene without disruption of the fine porous structure is demonstrated using an intense femtosecond-pulse laser. As a result of laser-matter interactions near ablation threshold fluence, high-energy ions are emitted, which cannot be produced by thermal dissociation of the molecules. The ion energy is produced by Coulomb explosion of the elements of (-CF_{2}-CF_{2-})n and the energy spectra of the ions show contributions from the Coulomb explosions of the ions rather than those of thermal expansion to generate high-energy ions. The dependence of ion energy on the laser fluence of a 180-fs pulse, compared with that of a 400-ps pulse, also suggests that the high-energy ions are accelerated by Coulomb explosio

Mechanism of femtosecond laser nano-ablation for metals

Metals have three ablation threshold fluences (high,middle and low-threshold fluence, here called) forfemtosecond laser pulses. In order to investigatethe physics of metal ablation under an intenseoptical field, the ions emitted from a laserirradiatedcopper surface were studied by time-offlightenergy spectroscopy. The low laser fluenceat which ions are emitted, Fth,L is 0.028 J/cm2, andtwo higher emission thresholds were identified atfluences of Fth,M =0.195 J/cm2 and Fth,H =0.470J/cm2. The relation between the number of emittedions per pulse Ni and laser fluence F was in goodagreement with Ni ∝F4 for Fth,L - Fth,M, Ni ∝F3 forFth,M - Fth,H, and Ni ∝F2 for ≥ Fth,H. Thedependence of ion production on laser energyfluence is explained well by multiphotonabsorption and optical field ionization.For fluence levels near the middle to high ablationthreshold, the formation of grating structures onmetal surfaces has been observed. The interspacesof grating structures were shorter than the laserwavelength, and the interspaces depend on fluencefor Mo and W with a 160 fs laser pulse. Thisphenomenon is well explained by the parametricdecay model proposed by Sakabe et al

Columnariose: etiologia, sinais clínicos e envio de amostras para análise laboratorial.

bitstream/item/42313/1/DOC109-columnariose.pd

Effects of Metal Hydride Coatings at the Electrodes on Neutron Production Rate in a Discharge-Type Fusion Neutron Source

A glow discharge (GD) fusion neutron source that utilizes nuclear fusion reactions of deuterium has been upgraded. The fusion reactions in this device mainly occur by collisions between the charged or neutral particles and the hydrogen isotopes trapped at the surface of electrodes. In addition, it is known that the metal hydride coating on the electrode enhances the neutron production rate (NPR). Therefore, the elemental distribution, including deuterium, in the depth direction on the electrode is an essential factor in neutron production. However, the distribution on the electrode has not been experimentally investigated. This study aims to analyze the distribution experimentally and indicate the effect of the metal hydride coatings. To achieve this purpose, we prepared the titanium (Ti)-coated cathode and the uncoated cathode, of which the base material was stainless steel. After that, the neutron production test was performed in the range of from 5-to 40-mA currents and from 20-to 60-kV applied voltage. This test indicated that the NPR was improved by coating the cathode with Ti than the uncoated cathode. In addition, depth profiling on the cathodes by glow discharge optical emission spectroscopy (GD-OES) was performed. While the analysis indicated that the concentration of deuterium on both cathodes was increased after the test, there was no significant difference in the concentration of deuterium between both cathodes. Furthermore, the concentration of Ti on the Ti-coated cathode was vastly decreased. The cause of these changes needs to be investigated

Tbx20 Is Required in Mid-Gestation Cardiomyocytes and Plays a Central Role in Atrial Development.

RationaleMutations in the transcription factor TBX20 (T-box 20) are associated with congenital heart disease. Germline ablation of Tbx20 results in abnormal heart development and embryonic lethality by embryonic day 9.5. Because Tbx20 is expressed in multiple cell lineages required for myocardial development, including pharyngeal endoderm, cardiogenic mesoderm, endocardium, and myocardium, the cell type-specific requirement for TBX20 in early myocardial development remains to be explored.ObjectiveHere, we investigated roles of TBX20 in midgestation cardiomyocytes for heart development.Methods and resultsAblation of Tbx20 from developing cardiomyocytes using a doxycycline inducible cTnTCre transgene led to embryonic lethality. The circumference of developing ventricular and atrial chambers, and in particular that of prospective left atrium, was significantly reduced in Tbx20 conditional knockout mutants. Cell cycle analysis demonstrated reduced proliferation of Tbx20 mutant cardiomyocytes and their arrest at the G1-S phase transition. Genome-wide transcriptome analysis of mutant cardiomyocytes revealed differential expression of multiple genes critical for cell cycle regulation. Moreover, atrial and ventricular gene programs seemed to be aberrantly regulated. Putative direct TBX20 targets were identified using TBX20 ChIP-Seq (chromatin immunoprecipitation with high throughput sequencing) from embryonic heart and included key cell cycle genes and atrial and ventricular specific genes. Notably, TBX20 bound a conserved enhancer for a gene key to atrial development and identity, COUP-TFII/Nr2f2 (chicken ovalbumin upstream promoter transcription factor 2/nuclear receptor subfamily 2, group F, member 2). This enhancer interacted with the NR2F2 promoter in human cardiomyocytes and conferred atrial specific gene expression in a transgenic mouse in a TBX20-dependent manner.ConclusionsMyocardial TBX20 directly regulates a subset of genes required for fetal cardiomyocyte proliferation, including those required for the G1-S transition. TBX20 also directly downregulates progenitor-specific genes and, in addition to regulating genes that specify chamber versus nonchamber myocardium, directly activates genes required for establishment or maintenance of atrial and ventricular identity. TBX20 plays a previously unappreciated key role in atrial development through direct regulation of an evolutionarily conserved COUPT-FII enhancer

Identification And Agreement Of First Turn Point By Mathematical Analysis Applied To Heart Rate, Carbon Dioxide Output And Electromyography.

The second heart rate (HR) turn point has been extensively studied, however there are few studies determining the first HR turn point. Also, the use of mathematical and statistical models for determining changes in dynamic characteristics of physiological variables during an incremental cardiopulmonary test has been suggested. To determine the first turn point by analysis of HR, surface electromyography (sEMG), and carbon dioxide output (VCO2) using two mathematical models and to compare the results to those of the visual method. Ten sedentary middle-aged men (53.9 ± 3.2 years old) were submitted to cardiopulmonary exercise testing on an electromagnetic cycle ergometer until exhaustion. Ventilatory variables, HR, and sEMG of the vastus lateralis were obtained in real time. Three methods were used to determine the first turn point: 1) visual analysis based on loss of parallelism between VCO2 and oxygen uptake (VO2); 2) the linear-linear model, based on fitting the curves to the set of VCO2 data (Lin-LinVCO2); 3) a bi-segmental linear regression of Hinkley's algorithm applied to HR (HMM-HR), VCO2 (HMM-VCO2), and sEMG data (HMM-RMS). There were no differences between workload, HR, and ventilatory variable values at the first ventilatory turn point as determined by the five studied parameters (p>0.05). The Bland-Altman plot showed an even distribution of the visual analysis method with Lin-LinVCO2, HMM-HR, HMM-VCO2, and HMM-RMS. The proposed mathematical models were effective in determining the first turn point since they detected the linear pattern change and the deflection point of VCO2, HR responses, and sEMG.17614-2