X-ray identification of fusion reaction products implanted in Al foils following 16O and 19F bombardment of 59Co foils

1980 ◽  
Vol 170 (1-3) ◽  
pp. 189-192
Author(s):  
A.W. Waltner ◽  
S.L. Varghese ◽  
J.E. Willis ◽  
S.M. Shafroth
Keyword(s):  
Fusion Reaction ◽  
Reaction Products ◽  
X Ray

scholarly journals Recent results on implosions directly driven at λ = 0·26-μm laser wavelength

1992 ◽  
Vol 10 (4) ◽  
pp. 573-583 ◽  
Author(s):  
M. Koenig ◽  
V. Malka ◽  
E. Fabre ◽  
P. Hammerling ◽  
A. Michard ◽  
...  
Keyword(s):  
Neutron Emission ◽  
Fusion Reaction ◽  
Laser Wavelength ◽  
Reconstruction Technique ◽  
Size Determination ◽  
Core Size ◽  
Reaction Products ◽  
X Ray ◽  
Emission Core ◽  
Α Particles

New diagnostics were implemented on the implosion experiments performed at LULI to improve our measurements of hydroefficiencies: Neutron chronometry gives the time of emission of the fusion reaction products as measured from the peak of the laser pulse; thereby making it possible to correlate the neutron emission with X-ray emission. Core imaging, based upon a maximum entropy reconstruction technique, leads to core size determination and also is a promising diagnostic for wall nonuniformities induced by irradiation conditions. A simple model is developed to retrieve experimental spectra of α-particles.

scholarly journals Joining of SiO2 glass and 316L stainless steel using Bi–Ag-based active solders

2020 ◽  
Vol 56 (4) ◽  
pp. 3444-3454
Author(s):  
Felix Weber ◽  
Markus Rettenmayr
Keyword(s):  
Stainless Steel ◽  
Cross Sections ◽  
316L Stainless Steel ◽  
Dissimilar Materials ◽  
Intermetallic Phases ◽  
Reaction Products ◽  
Cast State ◽  
Metallic Component ◽  
X Ray ◽  
Solder Interface

Abstract Active brazing is a commonly used method for joining dissimilar materials with at least one non-metallic component. In the present study, joining of SiO2 glass to 316L stainless steel was performed utilizing Bi–Ag-based solders. Ti up to a concentration of 4 and Mg up to 1 wt.% were added as active elements. Microstructures of the solder alloys in the as-cast state and of cross sections of the joined compounds were analysed using scanning electron microscopy and energy-dispersive X-ray spectroscopy. In the as-cast state of the solder, Ti is found in Bi–Ti intermetallic phases; Mg is partially dissolved in the fcc-(Ag) phase and additionally contained in a ternary Ag-Bi-Mg phase. After soldering, a tight joint was generated using several alloy compositions. Ti leads to the formation of reaction products at the steel/solder and glass/solder interfaces, and Mg is exclusively accumulated at the glass/solder interface.

Microtexture of shock reaction products of niobium and silica mixtures

1999 ◽  
Vol 14 (7) ◽  
pp. 3169-3174 ◽  
Author(s):  
Reiko Murao ◽  
Masae Kikuchi ◽  
Kiyoto Fukuoka ◽  
Eiji Aoyagi ◽  
Toshiyuki Atou ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Electron Microscope ◽  
Shock Compression ◽  
Pressure Range ◽  
Reaction Products ◽  
Small Particles ◽  
Powder Mixtures ◽  
X Ray ◽  
Transmission Electron

Shock compression experiments on powder mixtures of niobium metal and quartz were conducted for the pressure range of 30–40 GPa by a 25-mm single-stage propellant gun. Chemical reaction occurred above 35 GPa, and products were found to be mainly so-called “Cu3Au-type” Nb3Si, which contained a small amount of oxygen. Microtextures of the specimen were examined by scanning and transmission electron microscopy. A field-emission transmission electron microscope was used for energy-dispersive x-ray analysis of microtextures in small particles found in the SiO2 matrix, and various species with different Nb/Si ratio and oxygen content were shown to be produced through the nonequilibrium process of shock compression.

scholarly journals Acid-beta-glycerophosphatase reaction products in the central nervous system mitochondria following x-ray irradiation.

1975 ◽  
Vol 23 (6) ◽  
pp. 402-410 ◽  
Author(s):  
L Roizin ◽  
D Orlovskaja ◽  
J C Liu ◽  
A L Carsten
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Acid Phosphatase ◽  
Enzyme Reaction ◽  
Reaction Products ◽  
Huntington's Chorea ◽  
X Ray ◽  
System A ◽  
Chemical Lesion ◽  
The Central Nervous System

A survey of the literature to date on the enzyme histochemistry of intracellular organelles has not yielded any reference to the presence of acid phosphatase reaction products in the mammalian mitochondria of the central nervous system. A combination of Gomori's acid phosphatase mehtod, however, with standard electron microscopy has disclosed the presence of enzyme reaction products in the mitochondria of the central nervous system of rats from 2 hr to 22 weeks after x-ray irradiation, as well as in a cerebral biopsy performed on a patient affected by Huntington's chorea. No enzyme reaction products, on the other hand, were observed in serial sections that had been incubated in substrates either containing sodium fluoride or lacking in beta-glycerophosphate. The abnormal mitochondrial enzyme reaction (chemical lesion) is considered to be the consequenco of the pathologic process affecting the ultrastructural-chemical organization of the organelle.

scholarly journals Effects of Initial Water Content on Microstructure and Mechanical Properties of Lean Clay Soil Stabilized by Compound Calcium-Based Stabilizer

Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1933 ◽  
Author(s):  
Chenglong Yin ◽  
Wei Zhang ◽  
Xunli Jiang ◽  
Zhiyi Huang
Keyword(s):  
Water Content ◽  
Soil Stabilization ◽  
Clay Soil ◽  
Soil Aggregates ◽  
Optical Microscope ◽  
Initial Water Content ◽  
Reaction Products ◽  
Unconfined Compression Test ◽  
Initial Water ◽  
X Ray

Initial water content significantly affects the efficiency of soil stabilization. In this study, the effects of initial water content on the compressibility, strength, microstructure, and composition of a lean clay soil stabilized by compound calcium-based stabilizer were investigated by static compaction test, unconfined compression test, optical microscope observations, environment scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction. The results indicate that as the initial water content increases in the range studied, both the compaction energy and the maximum compaction force decrease linearly and there are less soil aggregates or agglomerations, and a smaller proportion of large pores in the compacted mixture structure. In addition, for specimens cured with or without external water supply and under different compaction degrees, the variation law of the unconfined compressive strength with initial water content is different and the highest strength value is obtained at various initial water contents. With the increase of initial water content, the percentage of the oxygen element tends to increase in the reaction products of the calcium-based stabilizer, whereas the primary mineral composition of the soil-stabilizer mixture did not change notably.

ARYL THIOCARBAMOYLATIONS OF PHTHALIDES AND X-RAY STUDIES OF THREE REACTION PRODUCTS

1996 ◽  
Vol 116 (1) ◽  
pp. 185-202 ◽  
Author(s):  
Wolfgang Dölling ◽  
Thomas Gildenast ◽  
Matthias Biedermann ◽  
Helmut Hartung
Keyword(s):  
Reaction Products ◽  
X Ray

scholarly journals Reactions of Titanocene- and Zirconocene-Bis(trimethylsilyl)acetylene Complexes with Selected Heterocyclic and Aromatic NH and OH Acid Compounds

2007 ◽  
Vol 72 (4) ◽  
pp. 475-491 ◽  
Author(s):  
Perdita Arndt ◽  
Vladimir V. Burlakov ◽  
Ulrike Jäger-Fiedler ◽  
Marcus Klahn ◽  
Anke Spannenberg ◽  
...  
Keyword(s):  
Bond Activation ◽  
Reaction Pathway ◽  
Reaction Products ◽  
X Ray ◽  
X Ray Crystallography

The titanocene complexes Cp'2Ti(η2-Me3SiC2SiMe3) (Cp' = Cp (1), Cp* (2)) react with pyrrole under the formation of the titanium(III) mono-N-pyrrolides Cp'2Ti(NC4H4) (Cp' = Cp (6), Cp* (7)); whereas the corresponding zirconocene system Cp2Zr(η2-Me3SiC2SiMe3)(thf) (3) forms in a different reaction pathway first the Cp2Zr(NC4H4)[C(SiMe3)=CH(SiMe3)] (8) and then the zirconium(IV) bis-N-pyrrolide Cp2Zr(NC4H4)2 (11). With Cp*2Zr(η2-Me3SiC2SiMe3) (4) and pyrrole, the zirconium(IV) mono-N-pyrrolide with an agostic alkenyl group Cp*2Zr(NC4H4)[C(SiMe3)=CH(SiMe3)] (9) was obtained. In the reaction of the ethylenebistetrahydroindenyl (ebthi) complex rac-(ebthi)Zr(η2-Me3SiC2SiMe3) (5) with 2,3,5,6-tetrafluoroaniline under N-H bond activation, a complex with an agostic alkenyl group rac-(ebthi)Zr(NH-C6HF4)[C(SiMe3)=CH(SiMe3)] (10) was formed. Compound 10 reacts with additional 2,3,5,6-tetrafluoroaniline to give the bisanilide rac-(ebthi)Zr(NH-C6HF4)2 (12) which was obtained directly from 5 with two equivalents of 2,3,5,6-tetrafluoroaniline. In reactions of complex 5 with unsubstituted aniline to rac-(ebthi)Zr(NH-C6H5)2 (13) and with pentafluorophenol to bisphenolate rac-(ebthi)Zr(O-C6F5)2 (14), no intermediates could be isolated. The new reaction products 6, 9, 10, 12, 13 and 14 were investigated by X-ray crystallography.

scholarly journals Multi Component Reactions under Increased Pressure: On the Mechanism of Formation of Pyridazino[5,4,3-de][1,6]naphthyridine Derivatives from Reaction of Malononitrile, Aldehyde and 2-Oxoglyoxalarylhydrazones in Q-Tubes

2017 ◽  
Author(s):  
Majdah A. AL-Johani ◽  
Khadijah M. Al-Zaydi ◽  
Sameera M. Mousally ◽  
Norah F. Alqahtani ◽  
Mohamed H. Elnagdi
Keyword(s):  
Crystal Structure ◽  
Reaction Pathway ◽  
Aromatic Aldehydes ◽  
Reaction Products ◽  
Mechanism Of Formation ◽  
X Ray ◽  
Alternate Pathway ◽  
Considerable Research ◽  
Increased Pressure ◽  
Chemical Evidence

The considerable biological and medicinal activities of pyridazines has stimulated considerable research on efficient syntheses of these derivatives. In the last decade, microwave irradiation has generally been used for the energy source. As demonstrated in recent studies, pressure reactor “Q-tubes” may be used to accelerate several of these reactions in a more optimal and safer manner (compared to microwaves). In these studies there has been postulated a pathway for the formation of pyridazino[5,4,3-de][1,6]naphthyridine derivatives . In this paper we consider this pathway, and an alternate pathway, for several reactions. Contrary to the suggestion in these studies the pathway in which initial dimerization of malononitrile was postulated could be excluded based on chemical evidence. The reactions performed were the reaction of arylhydrazonals 1a,b with benzylidinemalononitrile which afforded in Q-tube the 3-acyl-4-aryl-1-phenyl-6-amino-1,4-dihydropyridazines, and the reaction of arylhydrazonals 1a,b, malononitrile 9 and aromatic aldehydes 10a-g in Q-tubes which afforded the tricyclic systems 12a-n whose structure could be established by X-ray crystal structure determination. In conclusion, we have added to the work of the recent studies by excluding a reaction pathway for one of their reaction products.

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