scholarly journals Unbeeinflußbarkeit ihrer Wirkung auf Ribonuclease durch Cystamin und tiefe Temperaturen

1966 ◽  
Vol 21 (12) ◽  
pp. 1165-1170 ◽  
Author(s):  
H. Jung

Slow protons having energies below 1.5 keV dissipate their kinetic energy in matter through elastic nuclear collisions. By this process atoms are displaced out from their original positions in macromolecules. This was recently shown to cause biological damage with high efficiency. Experiments are described to test the possibility of modifying the sensitivity of ribonuclease towards elastic collisions by protective agents and by low temperatures. When cystamine is present during irradiation dry ribonuclease is protected against the action of “ionizing” fast protons (2 MeV), the dose reduction factor being 1.8. But no protection is observed when inactivation is achieved by elastic nuclear collisions (proton energy 1 keV and 1.4 keV). Similar results were obtained when the irradiations were carried out at different temperatures. Using 2 MeV protons the radiosensitivity of ribonuclease was found to be 3 times higher at room temperature than at 125 °K, but when using slow protons of 1.4 keV energy the inactivation cross section turned out to be independent of temperature. This shows that the action of elastic nuclear collisions can be modified neither by cystamine nor by low temperatures.

Materials ◽  
2021 ◽  
Vol 14 (2) ◽  
pp. 431
Author(s):  
Giorgio Turri ◽  
Scott Webster ◽  
Michael Bass ◽  
Alessandra Toncelli

Spectroscopic properties of neodymium-doped yttrium lithium fluoride were measured at different temperatures from 35 K to 350 K in specimens with 1 at% Nd3+ concentration. The absorption spectrum was measured at room temperature from 400 to 900 nm. The decay dynamics of the 4F3/2 multiplet was investigated by measuring the fluorescence lifetime as a function of the sample temperature, and the radiative decay time was derived by extrapolation to 0 K. The stimulated-emission cross-sections of the transitions from the 4F3/2 to the 4I9/2, 4I11/2, and 4I13/2 levels were obtained from the fluorescence spectrum measured at different temperatures, using the Aull–Jenssen technique. The results show consistency with most results previously published at room temperature, extending them over a broader range of temperatures. A semi-empirical formula for the magnitude of the stimulated-emission cross-section as a function of temperature in the 250 K to 350 K temperature range, is presented for the most intense transitions to the 4I11/2 and 4I13/2 levels.


1935 ◽  
Vol 35 (3) ◽  
pp. 437-448 ◽  
Author(s):  
A. E. Platt

1. The survival of coliform organisms was studied in river water, either raw or sterilised, kept at different temperatures.2. For determining the coliform count and the differentialcoli-aerogenescount in sterilised river water, direct plating of the water on agar, with subsequent study of a number of colonies picked at random, was used. For raw river water the rapid method described by Wilson and his colleagues (1935) was used, which obviates the necessity of plating and of colonial examination.3. WhenBact. coliandBact. aerogeneswere held in stored river water, which was protected from agitation, they underwent a gradual decrease in numbers and finally disappeared. At 37°C. they died out rapidly, but survived for a much longer time at temperatures in the neighbourhood of 0°C. They were able to survive longer in sterile water than in raw water.4. Observations, however, made on water kept at room temperature and subjected to gentle aeration showed that not only did the organisms not die out, but that they actually multiplied, so that their numbers were considerably higher at the end of two months than at the beginning of the experiment.5. In raw river water coliform bacilli survived longer at room temperature when kept in the dark than in daylight.6. On the whole,aerogenes1proved more resistant thanBact. colito the environmental conditions provided. This was particularly noticeable in samples kept at room temperature (18°C.). In samples of raw water kept at 37°C.aerogenesproved slightly more resistant thancoli, while at 0–2°C. the reverse was true.7. The general conclusion seems to be that, except at very low temperatures,aerogenesis likely to survive longer in raw river water thanBact. coli.8. This conclusion is clearly of importance in the interpretation of thecoli-aerogenesresults in water analysis.


2007 ◽  
Vol 72 (7) ◽  
pp. 713-722 ◽  
Author(s):  
Slavisa Putic ◽  
Marina Stamenovic ◽  
Branislav Bajceta ◽  
Predrag Stajcic ◽  
Srdjan Bosnjak

The aim of this paper is to present the influence of high and low temperatures on the impact properties glass-epoxy composites. The impact strength an is presented for four different glass-epoxy composite structures at three different temperatures, i.e., at room temperature t=20?C, at an elevated temperature t=+50?C and at a low temperature t=-50?C. Standard mechanical testing was carried out on the composite materials with specific masses of reinforcement of 210 g m-2 and 550 g m-2 and orientations 0?/90? and ?45?. Micromechanical analysis of the failure was performed in order to determine real models and mechanisms of crack and temperature influence on the impact properties. .


2016 ◽  
Vol 1133 ◽  
pp. 50-54 ◽  
Author(s):  
Siti Noorzidah Mohd Sabri ◽  
Syazana Abu Bakar ◽  
Abdul Yazid Abdul Manaf ◽  
Siti Farhana Hisham ◽  
Mohamad Azmirruddin Ahmad ◽  
...  

The purpose of this study was to prepare biphasic granules containing gypsum and carbonated apatite at low temperatures. The biphasic granules were prepared using dissolution-precipitation technique at three different temperatures 30°C, 40°C and 50°C. Characterization of the biphasic granules was determined by multiple analytical methods such as X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier Transform Infra-red (FTIR), and CHN Analysis. The obtained granules were determined by XRD as biphasic granules containing bone apatite and gypsum. The cross-section of biphasic granules was observed by SEM. The formed bone apatite was identified as B-Type carbonated apatite using FTIR The carbonate content in biphasic granules fabricated at 30°C, 40°C and 50°C were recorded by CHN analysis as 5.0 wt%, 6.1 wt% and 6.25 wt%, respectively.


1967 ◽  
Vol 22 (3) ◽  
pp. 313-320 ◽  
Author(s):  
Wolfgang Günther ◽  
Horst Jung

The radiosensitivity of dry ribonuclease was determined at various temperatures ranging from 90 °K to 300 °K and using 60Co gamma-radiation, 2 MeV protons, and 2 MeV deuterons. The cross section for the inactivation of RNase S (T) is, in this range, given as a function of temperature byS(T) =S0+S1·e-Ea/RT.For inactivation of ribonuclease with Co gamma-rays we found S0=0 and Ea=1000 cal/mole; S1= =0.125 Mrad-1 when irradiation is carried out in vacuo, and S1=0.265 Mrad-1 in oxygen. With protons and deuterons the following values were determined: S0=1.28·10-14 cm2, S1=19.5·10-14 cm2, Ea=1050 cal/mole for 2 MeV protons; S0=2.45·10-14 cm2, S1=31·10-14 cm2, and Ea = 1050 cal/mole for 2 MeV deuterons. Furthermore, by analysis of some recent data from the literature we found that the cross section for inactivation by ionizing radiation of various enzymes, bacteriophages, and bacterial spores in the range from 4 °K to temperatures higher than room temperature can satisfactorily be described by the more general equationS(T) =S0+S1·e-E₁/RT+S2·e-E₂/RT,with E1=1 kcal/mole and E2=4 kcal/mole being constant for all objects and for all circumambient conditions tested. This correlation between inactivation cross section S (T) and temperature T shows three mechanisms of inactivation to occur in biological objects: one (S0) being independent of temperature, while the two others have apparent activation energies of 1 kcal/mole and 4 kcal/mole, respectively.


1968 ◽  
Vol 23 (7) ◽  
pp. 949-952 ◽  
Author(s):  
Klaus Kürzinger ◽  
Horst Jung

The radiosensitivity of dry ribonuclease was determined at various temperatures between 120 °K and 440 °K using 2 MeV protons. Within this temperature range the inactivation cross section S (T) of ribonuclease may be described as a function of temperature by the expression S(T) = (1.28 + 16·e-1000/RT+14000·e-6500/7RT)·10-14 cm2 .This result indicates that the observed radiation damage to ribonuclease is produced by three different mechanisms, one being independent of temperature, the other two having apparent activation energies of 1 kcal/mole and 6.5 kcal/mole, respectively. From these relatively small activation energies the conclusion may be drawn that radical reactions contribute to the inactivation of enzymes in the dry state. Experiments with Co gamma radiation showed that the radiosensitivity of ribonuclease at 77 °K depends on dose rate; at room temperature a dose rate effect was not observed.


1998 ◽  
Vol 29 (3) ◽  
pp. 164-166 ◽  
Author(s):  
Francisco Cleber Sousa Vieira ◽  
Ely Nahas

The enzymatic activity of soil samples stored at temperatures of 5 to -12oC and at room temperature for 0-32 weeks was determined. While alkaline phosphatase and dehydrogenase activity was decreased compared to control in samples stored at low temperatures, acid phosphatase activity showed no significant change.


Author(s):  
M. H. Rhee ◽  
W. A. Coghlan

Silicon is believed to be an almost perfectly brittle material with cleavage occurring on {111} planes. In such a material at room temperature cleavage is expected to occur prior to any dislocation nucleation. This behavior suggests that cleavage fracture may be used to produce usable flat surfaces. Attempts to show this have failed. Such fractures produced in semiconductor silicon tend to occur on planes of variable orientation resulting in surfaces with a poor surface finish. In order to learn more about the mechanisms involved in fracture of silicon we began a HREM study of hardness indent induced fractures in thin samples of oxidized silicon.Samples of single crystal silicon were oxidized in air for 100 hours at 1000°C. Two pieces of this material were glued together and 500 μm thick cross-section samples were cut from the combined piece. The cross-section samples were indented using a Vicker's microhardness tester to produce cracks. The cracks in the samples were preserved by thinning from the back side using a combination of mechanical grinding and ion milling.


1977 ◽  
Vol 16 (01) ◽  
pp. 30-35 ◽  
Author(s):  
N. Agha ◽  
R. B. R. Persson

SummaryGelchromatography column scanning has been used to study the fractions of 99mTc-pertechnetate, 99mTcchelate and reduced hydrolyzed 99mTc in preparations of 99mTc-EDTA(Sn) and 99mTc-DTPA(Sn). The labelling yield of 99mTc-EDTA(Sn) chelate was as high as 90—95% when 100 μmol EDTA · H4 and 0.5 (Amol SnCl2 was incubated with 10 ml 99mTceluate for 30—60 min at room temperature. The study of the influence of the pH-value on the fraction of 99mTc-EDTA shows that pH 2.8—2.9 gave the best labelling yield. In a comparative study of the labelling kinetics of 99mTc-EDTA(Sn) and 99mTc- DTPA(Sn) at different temperatures (7, 22 and 37°C), no significant influence on the reduction step was found. The rate constant for complex formation, however, increased more rapidly with increased temperature for 99mTc-DTPA(Sn). At room temperature only a few minutes was required to achieve a high labelling yield with 99mTc-DTPA(Sn) whereas about 60 min was required for 99mTc-EDTA(Sn). Comparative biokinetic studies in rabbits showed that the maximum activity in kidneys is achieved after 12 min with 99mTc-EDTA(Sn) but already after 6 min with 99mTc-DTPA(Sn). The long-term disappearance of 99mTc-DTPA(Sn) from the kidneys is about five times faster than that for 99mTc-EDTA(Sn).


2019 ◽  
Author(s):  
Shuyuan Zheng ◽  
Taiping Hu ◽  
Xin Bin ◽  
Yunzhong Wang ◽  
Yuanping Yi ◽  
...  

Pure organic room temperature phosphorescence (RTP) and luminescence from nonconventional luminophores have gained increasing attention. However, it remains challenging to achieve efficient RTP from unorthodox luminophores, on account of the unsophisticated understanding of the emission mechanism. Here we propose a strategy to realize efficient RTP in nonconventional luminophores through incorporation of lone pairs together with clustering and effective electronic interactions. The former promotes spin-orbit coupling and boost the consequent intersystem crossing, whereas the latter narrows energy gaps and stabilizes the triplets, thus synergistically affording remarkable RTP. Experimental and theoretical results of urea and its derivatives verify the design rationale. Remarkably, RTP from thiourea solids with unprecedentedly high efficiency of up to 24.5% is obtained. Further control experiments testify the crucial role of through-space delocalization on the emission. These results would spur the future fabrication of nonconventional phosphors, and moreover should advance understanding of the underlying emission mechanism.<br>


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