scholarly journals Determination of protein loss during aqueous and phase partition fixation using formalin and glutaraldehyde.

1984 ◽  
Vol 32 (10) ◽  
pp. 1107-1112 ◽  
Author(s):  
E T Mays ◽  
R C Feldhoff ◽  
G S Nettleton
Keyword(s):  
Organic Solvent ◽  
Aqueous Phase ◽  
Protein Loss ◽  
Protein Retention ◽  
Phase Partition ◽  
Better Than

In phase partition fixation tissue is immersed in an organic solvent at equilibrium with an aqueous phase containing a fixing agent. By using radioisotope labeling techniques the effects of phase partition fixation on protein retention during fixation of tissue with formalin and glutaraldehyde have been determined and compared with those of standard aqueous fixation using these fixatives. It has been shown that retention of protein in tissue during phase partition fixation was as good or better than during aqueous fixation. Improved retention provides further evidence that phase partition fixation may be a useful alternative to aqueous fixation.

scholarly journals Determination of lipid loss during aqueous and phase partition fixation using formalin and glutaraldehyde.

1986 ◽  
Vol 34 (4) ◽  
pp. 437-441 ◽  
Author(s):  
D P Leist ◽  
G S Nettleton ◽  
R C Feldhoff
Keyword(s):  
Total Lipid ◽  
Formalin Fixation ◽  
Phase Partition ◽  
Fixation Techniques ◽  
Osmotic Effects ◽  
Better Than

Phase partition fixation permits fixation of tissue in a nonaqueous environment, thus eliminating osmotic effects. It was shown in an earlier investigation that retention of protein in liver blocks can be improved by phase partition fixation. By using radioisotopic labeling techniques, the effects of phase partition fixation on lipid retention during fixation, dehydration, and clearing have been determined and compared with those of standard aqueous fixation techniques. In this article we show that retention of total lipid in liver blocks following phase partition fixation using formalin was comparable to or better than that with aqueous formalin fixation and processing. Fixation with glutaraldehyde using phase partition fixation resulted in somewhat greater loss of total lipid than that observed for aqueous buffered glutaraldehyde-fixed blocks.

A comparison of spectrophotometric methods for the determination of uranium

1991 ◽  
Vol 56 (4) ◽  
pp. 774-784 ◽  
Author(s):  
Luděk Jančář ◽  
Irena Jančářová ◽  
Josef Havel
Keyword(s):  
Organic Solvent ◽  
Aqueous Phase ◽  
State Standard ◽  
Surface Waters ◽  
Waste Waters ◽  
Triphenylmethane Dyes ◽  
Spectrophotometric Methods ◽  
Model Sample ◽  
Uranium Industry

Some spectrometric and extraction photometric methods for the determination of uranium were compared using pure solutions, a model sample and samples of surface waters and waste waters; the characteristics examined included sensitivity, accuracy, repeatability, time demands and tediousness. Among the most sensitive methods are those based on the use of triphenylmethane dyes in the presence of surfactants; uranium is separated from associate ions by extraction into tri-n-octylamine in an organic solvent and subsequently re-extracted into an aqueous phase. The results compare well with those attained by using methods given in the Czechoslovak State Standard and in the standard of the Czechoslovak Uranium Industry corporation.

Time and Latitude in South Africa

1972 ◽  
Vol 1 ◽  
pp. 27-38
Author(s):  
J. Hers
Keyword(s):  
South Africa ◽  
Cape Town ◽  
Astronomical Observations ◽  
Royal Observatory ◽  
The Republic ◽  
Astronomical Determination ◽  
Limited Accuracy ◽  
Better Than

In South Africa the modern outlook towards time may be said to have started in 1948. Both the two major observatories, The Royal Observatory in Cape Town and the Union Observatory (now known as the Republic Observatory) in Johannesburg had, of course, been involved in the astronomical determination of time almost from their inception, and the Johannesburg Observatory has been responsible for the official time of South Africa since 1908. However the pendulum clocks then in use could not be relied on to provide an accuracy better than about 1/10 second, which was of the same order as that of the astronomical observations. It is doubtful if much use was made of even this limited accuracy outside the two observatories, and although there may – occasionally have been a demand for more accurate time, it was certainly not voiced.

Determination of trace concentrations of copper by FIA-FAAS after preconcentration on chelating sorbents

1989 ◽  
Vol 54 (7) ◽  
pp. 1785-1794 ◽  
Author(s):  
Vlastimil Kubáň ◽  
Josef Komárek ◽  
Zbyněk Zdráhal
Keyword(s):  
Sampling Frequency ◽  
Copper Determination ◽  
Flow Rates ◽  
Sample Injection ◽  
Injection Flow ◽  
Chelating Sorbents ◽  
Set Up ◽  
Trace Concentrations ◽  
Better Than

A FIA-FAAS apparatus containing a six-channel sorption equipment with five 3 x 26 mm microcolumns packed with Spheron Oxin 1 000, Ostsorb Oxin and Ostsorb DTTA was set up. Combined with sorption from 0.002M acetate buffer at pH 4.2 and desorption with 2M-HCl, copper can be determined at concentrations up to 100, 150 and 200 μg l-1, respectively. For sample and eluent flow rates of 5.0 and 4.0 ml min-1, respectively, and a sample injection time of 5 min, the limit of copper determination is LQ = 0.3 μg l-1, repeatability sr is better than 2% and recovery is R = 100 ± 2%. The enrichment factor is on the order of 102 and is a linear function of time (volume) of sample injection up to 5 min and of the sample injection flow rate up to 11 ml min-1 for Spheron Oxin 1 000 and Ostsorb DTTA. For times of sorption of 60 and 300 s, the sampling frequency is 70 and 35 samples/h, respectively. The parameters of the FIA-FAAS determination (acetylene-air flame) are comparable to or better than those achieved by ETA AAS. The method was applied to the determination of traces of copper in high-purity water.

Determination of Dimetridazole and Ipronidazole in Feeds at Cross-Contamination Levels

1988 ◽  
Vol 71 (3) ◽  
pp. 474-477 ◽  
Author(s):  
Duane D Hughes
Keyword(s):  
Thin Layer ◽  
Rapid Method ◽  
Aqueous Phase ◽  
Borate Buffer ◽  
Cross Contamination ◽  
Chromatographic System ◽  
Arsanilic Acid ◽  
Contamination Levels ◽  
Benzene Extract

Abstract A rapid method for the determination of dimetridazole and ipronidazole in feeds is described. The compounds are extracted from a borate buffer (pH 8.65) with benzene, partitioned into IN HC1, and then partitioned back into benzene from a basic aqueous phase. The benzene extract is concentrated and injected onto a nonpolar (Apiezon L) gas chromatographic column for determination by 63Ni electroncapture detection. Recoveries from feeds of various composition, spiked at 0.2 ppm with both dimetridazole and ipronidazole, ranged from 70 to 115%; for the same feeds spiked at 1 ppm or more, the recoveries were greater than 80%. Carbadox, furazolidone, levamisole, oxytetracycline, chlortetracycline, sulfamethazine, sulfaquinoxaline, arsanilic acid, piperazine, penicillin, and commonly added vitamins and minerals do not interfere. A 2-dimensional thin layer chromatographic system is presented as a means of additional identification.

scholarly journals Measuring the quartic Higgs self-coupling at a multi-TeV muon collider

2020 ◽  
Vol 2020 (9) ◽  
Author(s):  
M. Chiesa ◽  
F. Maltoni ◽  
L. Mantani ◽  
B. Mele ◽  
F. Piccinini ◽  
...  
Keyword(s):  
Higgs Boson ◽  
Center Of Mass ◽  
Mass Energy ◽  
Simple Analysis ◽  
Proton Proton ◽  
Coupling Interaction ◽  
Center Of Mass Energy ◽  
Muon Collider ◽  
Better Than

Abstract Measuring the shape of the Higgs boson potential is of paramount importance, and will be a challenging task at current as well as future colliders. While the expectations for the measurement of the trilinear Higgs self-coupling are rather promising, an accurate measurement of the quartic self-coupling interaction is presently considered extremely challenging even at a future 100 TeV proton-proton collider. In this work we explore the sensitivity that a muon collider with a center of mass energy in the multi-TeV range and luminosities of the order of 1035cm−2s−1, as presently under discussion, might provide, thanks to a rather large three Higgs-boson production and to a limited background. By performing a first and simple analysis, we find a clear indication that a muon collider could provide a determination of the quartic Higgs self-coupling that is significantly better than what is currently considered attainable at other future colliders.

scholarly journals Performance of the SoLid reactor neutrino detector

2019 ◽  
Vol 219 ◽  
pp. 08003
Author(s):  
Maja Verstraeten
Keyword(s):  
Quality Control ◽  
Energy Resolution ◽  
Neutrino Detector ◽  
Channel Response ◽  
In Situ Calibration ◽  
Reactor Neutrino ◽  
Li Isotope ◽  
Better Than

The SoLid Collaboration is currently operating a 1.6 ton neutrino detector near the Belgian BR2 reactor. Its main goal is the observation of the oscillation of electron antineutrinos to previously undetected flavour states. The highly segmented SoLid detector employs a compound scintillation technology based on PVT scintillator in combination with LiF-ZnS(Ag) screens containing the 6Li isotope. The experiment has demonstrated a channel-to-channel response that can be controlled to the level of a few percent, an energy resolution of better than 14% at 1 MeV, and a determination of the interaction vertex with a precision of 5 cm. This contribution highlights the major outcomes of the R&D program, the quality control during component manufacture and integration, the current performance and stability of the full-scale system, as well as the in-situ calibration of the detector with various radioactive sources.

HPLC Determination of Furfural after Preliminary Extraction to Aqueous Phase

2007 ◽  
Vol 30 (14) ◽  
pp. 2081-2093 ◽  
Author(s):  
Hossein Sid Kalal ◽  
Mohamad Khayatzadeh Mahani ◽  
Mohamad Ghanadi Maragheh ◽  
Marzieh Chaloosi
Keyword(s):  
Aqueous Phase ◽  
Hplc Determination ◽  
Preliminary Extraction

scholarly journals The Application of Baum-Welch Algorithm in Multistep Attack

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Yanxue Zhang ◽  
Dongmei Zhao ◽  
Jinxing Liu
Keyword(s):  
Markov Model ◽  
Hidden Markov Model ◽  
Hidden Markov Models ◽  
Viterbi Algorithm ◽  
Markov Models ◽  
Hidden Markov ◽  
Simulation Experiments ◽  
Forward Algorithm ◽  
Better Than

The biggest difficulty of hidden Markov model applied to multistep attack is the determination of observations. Now the research of the determination of observations is still lacking, and it shows a certain degree of subjectivity. In this regard, we integrate the attack intentions and hidden Markov model (HMM) and support a method to forecasting multistep attack based on hidden Markov model. Firstly, we train the existing hidden Markov model(s) by the Baum-Welch algorithm of HMM. Then we recognize the alert belonging to attack scenarios with the Forward algorithm of HMM. Finally, we forecast the next possible attack sequence with the Viterbi algorithm of HMM. The results of simulation experiments show that the hidden Markov models which have been trained are better than the untrained in recognition and prediction.

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