Modal dispersion due to photon–plasmon coupling in a SNOM tip

The mesoscopic effect of spectral modulation is used to experimentally investigate the possible effect of a metal-coated SNOM tip on the intermodal dispersion of an optical fiber. Highly regular modulation registered in a fixed spectral region of the broadband light transmitted by a 200 nm SNOM tip yields the value of optical path difference (OPD) in the two-mode model. To investigate the origin of this OPD a series of spectral measurements accompanied with a gradual reduction of the multimode fiber tail length has been performed. The results indicate that the observed OPD consists of two clearly distinguishable contributions: the OPD in the non-coated multimode fiber and the OPD in the metal-coated SNOM tip. The first one is a result of the inherent modal dispersion of an optical fiber. A numerical consideration shows that the second one can be attributed to a mode-dependent contribution of surface plasmon polaritons: one of the two modes couples to plasmons stronger than the other one, resulting in a remarkably slower propagation. This leads to a completely different value of intermodal dispersion, which actually changes its sign in the SNOM tip. Proposed is a logical explanation for such kind of a sign-switching behavior.     

Flow boiling visualization in a vertical circular minichannel at high vapor quality

This paper reports on an experimental study of saturated flow boiling of R134a inside a circular vertical quartz tube coated with a transparent heater. The inner diameter of the tube was 1.33 mm and the heated length 235.5 mm. The flow pattern at high vapor qualities and the dryout of the liquid film were studied using a high speed CCD camera at the mass fluxes 47.4 and 124.4 kg/m² s in up flow at 6.425 bar. The heat fluxes ranged from 5 to 13.6 kW/m² for the lower mass flux and from 20 to 32.4 kW/m² for the higher mass flux.

The behavior of the flow close to dryout was found to be different at low and high mass flux. At low mass flux the location of the liquid front fluctuated with waves passing high up in the tube. In between the waves, a thin film was formed, slowly evaporating without breaking up.

At high mass flux the location of the liquid front was more stable. In this case the liquid film was seen to break up into liquid streams and dry zones on the tube wall.     

Entropie und Erzeuger in dynamischen VerbÄnden

Ohne Zusammenfassung     

Eine klasse topologischer Fastkörperebenen

Ohne ZusammenfassungAus dem Nachlaß. Für den Druck vorbereitet von Theo Grundhöfer (Tübingen) und Heinz Lüneburg (Kaiserslautern).     

THE PHOTOTOXICITY OF PHENYLHEPTATRIYNE: OXYGEN-DEPENDENT HEMOLYSIS OF HUMAN ERYTHROCYTES AND INACTIVATION OF Escherichia coli

Abstract— Phenylheptatriyne (PHT) plus near-ultraviolet light(320–400 nm; NUV) hemolyzed human erythrocytes in an oxygen dependent manner. When the phototoxicity of PHT plus NUV was tested with a series of Escherichia coli strains carrying all four possible combinations of genes controlling excision proficiency ( uvrA6 vs uvrA ⁺) and catalase activity (HPII, katF vs katF *), the membrane was found to be an important lethal target. Consistent with this observation. PHT plus NUV did not induce histidine independent ( his-4 ⁺) mutations in the four tester strains (RT7h-RT10h). Using tester strain RT10h, it was shown that there was no inactivation by PHT plus NUV in nitrogen. Results of experiments with an E. coli fatty acid auxotroph (K1060) treated with PHT plus NUV are also consistent with membrane proteins being the chief targets for attack. Radicals were formed during the photolysis of PHT plus NUV in aqueous solutions, both in the presence of air and under nitrogen. Since PHT plus NUV did not hemolyze erythrocytes or inactivate E. coli cells under nitrogen, these radicals are not cytotoxic.     

A monolithic PNGase F enzyme microreactor enabling glycan mass mapping of glycoproteins by mass spectrometry

We demonstrate a simple and rapid single-step method to fabricate an enzyme microreactor incorporating the N-glycosidase PNGase F (peptide-N-glycosidase F) into a porous polymer-based monolith. The monolith is contained in a capillary format, while the enzyme reactor is ready to use within 1 h of preparation. The monomers making up the monolith, including N-acryloxysuccinimide for covalent immobilization of the enzyme, are mixed with PNGase F and introduced into the column by capillary force for polymerization/immobilization. Glycoproteins (ribonuclease B, asialofetuin, alpha1-acid glycoprotein, and ovalbumin) perfused through the PNGase F reactor were shown to be effectively deglycosylated on a time-scale of seconds/low minutes using low nanogram to microgram per microliter concentration (corresponding to a total sample consumption of 0.1-20 microg of a glycoprotein). The reactor enzyme activity was shown to be reproducible for at least 8 weeks when used and stored at room temperature. Evaluation was performed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.