From the Sea to Hydrobromic Acid: Polydopamine Layer as Corrosion Protective Layer on Platinum Electrocatalyst

2018 ◽  
Vol 1 (9) ◽  
pp. 4678-4685 ◽  
Author(s):  
Gregory Gershinsky ◽  
Pilkhaz Nanikashvili ◽  
Ran Elazari ◽  
David Zitoun
Keyword(s):  
Hydrobromic Acid ◽  
Protective Layer ◽  
Platinum Electrocatalyst

Development of imaging plate for a TEM and its characteristics

1989 ◽  
Vol 47 ◽  
pp. 100-101
Author(s):  
N. Mori ◽  
T. Oikawa ◽  
Y. Harada ◽  
J. Miyahara ◽  
T. Matsuo
Keyword(s):  
Dynamic Range ◽  
Protective Layer ◽  
High Sensitivity ◽  
Imaging Plate ◽  
Phosphor Layer ◽  
Imaging Device ◽  
X Ray Imaging ◽  
New Type ◽  
Basic Characteristics ◽  
Reading System

The Imaging Plate (IP) is a new type imaging device, which was developed for diagnostic x ray imaging. We have reported that usage of the IP for a TEM has many merits; those are high sensitivity, wide dynamic range, and good linearity. However in the previous report the reading system was prototype drum-type-scanner, and IP was also experimentally made, which phosphor layer was 50μm thick with no protective layer. So special care was needed to handle them, and they were used only to make sure the basic characteristics. In this article we report the result of newly developed reading, printing system and high resolution IP for practical use. We mainly discuss the characteristics of the IP here. (Precise performance concerned with the reader and other system are reported in the other article.)Fig.1 shows the schematic cross section of the IP. The IP consists of three parts; protective layer, phosphor layer and support.

Study on preferred crystal orientations of Mg-Zr-O composite protective layer in AC-PDP

2006 ◽  
Vol 36 (2) ◽  
pp. 111-117 ◽  
Author(s):  
G. Bingang ◽  
L. Chunliang ◽  
S. Zhongxiao ◽  
L. Liu ◽  
F. Yufeng ◽  
...  
Keyword(s):  
Protective Layer ◽  
Crystal Orientations

New atmospheric corrosion inhibitor of aluminum alloy D16

2020 ◽  
pp. 38-46
Author(s):  
A.M. Semiletov ◽  
◽  
Yu.B. Makarychev ◽  
A.A. Chirkunov ◽  
L.P. Kazansky ◽  
...  
Keyword(s):  
Aluminum Alloy ◽  
Corrosion Inhibitor ◽  
Atmospheric Corrosion ◽  
Protective Layer ◽  
Humid Atmosphere ◽  
Water Condensation ◽  
Equimolar Composition ◽  
Aluminum Hydroxides ◽  
Daily Water ◽  
20 Nm

The application of mixed corrosion inhibitor (CI), which is an equimolar composition of oleoyl sarcosinate (SOS) and sodium flufenamate (SFF), for protection of D16 aluminum alloy from atmospheric corrosion has been studied. The polarization measurements used to assess the effectiveness of preliminary passivation of the alloy with solutions of SOS, SFF and their composition showed significant advantages of mixed CI. The XPS method was used to study features of CI adsorption on the surface of D16 alloy. It has been established that upon adsorption of SOS and SFF separately a monolayer is formed, firmly bonded to the alloy surface, thickness of which is not exceeding 2.6—3.2 nm. After the joint adsorption of these CI, the layer thickness reaches 12—20 nm. The composition of this layer includes a considerable amount of Al3+ ions (~20%) related to their compounds with SFF and SOS, as well as to aluminum hydroxides. A possible mechanism for the formation of such a protective layer is proposed. The results of corrosion tests in a humid atmosphere with daily water condensation on samples of D16 alloy confirmed the high protective ability of the mixed CI film.

Application of Automated FIB for TEM Sample Preparation in Semiconductor Failure Analysis

2014 ◽  
Author(s):  
Jie Zhu ◽  
Soo Sien Seah ◽  
Irene Tee ◽  
Bing Hai Liu ◽  
Eddie Er ◽  
...  
Keyword(s):  
Sample Preparation ◽  
Success Rate ◽  
Protective Layer ◽  
Factors Affecting ◽  
Dual Beam ◽  
Lamella Thickness ◽  
Surface Patterns ◽  
Working Parameters ◽  
Practical Factors ◽  
High Flexibility

Abstract In this paper, we describe automated FIB for TEM sample preparation using iFast software on a Helios 450HP dual-beam system. A robust iFast automation recipe needs to consider as many variables as possible in order to ensure consistent sample quality and high success rate. Variations mainly come from samples of different materials, structures, surface patterns, surface topography and surface charging. The recipe also needs to be user-friendly and provide high flexibility by allowing users to choose preferable working parameters for specific types of samples, such as: grounding, protective layer coating, milling steps, and final TEM lamella thickness/width. In addition to the iFast recipe, other practical factors affecting automation success rate are also discussed and highlighted.

Solification with Hydrobromic Acid as a Factor Defining the Antiarrhythmic Effect of Lappaconitine Derivatives

2009 ◽  
Vol 6 (7) ◽  
pp. 475-477 ◽  
Author(s):  
T. Tolstikova ◽  
A. Bryzgalov ◽  
I. Sorokina ◽  
S. Osadchii ◽  
E. Shults ◽  
...  
Keyword(s):  
Hydrobromic Acid ◽  
Antiarrhythmic Effect

Participation of 19-ester groups in the cleavage of 2α,3α- and 5α,6α-steroid epoxides. A case of competition between participation and external nucleophile attack

1979 ◽  
Vol 44 (5) ◽  
pp. 1496-1509 ◽  
Author(s):  
Pavel Kočovský ◽  
Václav Černý
Keyword(s):  
Perchloric Acid ◽  
Hydrobromic Acid ◽  
Ester Group ◽  
Carbonyl Oxygen ◽  
Cyclic Carbonate ◽  
Cyclic Ether ◽  
Normal Reaction ◽  
Neighboring Group ◽  
Ether Oxygen ◽  
The Difference

Acid cleavage of the acetoxy epoxide IIIa with aqueous perchloric acid or hydrobromic acid gave two types of products, i.e. the diol Va or the bromohydrin VIa, and the cyclic ether VIII. The latter compound arises by participation of ether oxygen of the ester group. On reaction with perchloric acid the epoxide IVa gave the diol XIIIa as a product of a normal reaction and the isomeric diol Xa as a product arising by intramolecular participation of the carbonyl oxygen of the 19-acetoxy group. Participation of the 19-ester group is confirmed by the formation of the cyclic carbonate XI when the 19-carbonate IVb is treated analogously. On reaction with hydrobromic acid, the epoxide IVa gave solely the bromohydrin XIVa as a product of the normal reaction course. Discussed is the similarity of these reactions with electrophilic additions to the related 19-acetoxy olefins I and II, the mechanism, the difference in behavior of both epoxides III and IV, the dependence of the product ratio on the nucleophility of the attacking species, and the competition between participation of an ambident neighboring group and an external nucleophile attack.

Participation of 19-substituents in electrophilic additions to 6,7-unsaturated 5α-cholestane and B-homo 5α-cholestane derivatives; A case of competition between the participation of an ambident neighboring group and external nucleophile attack

1980 ◽  
Vol 45 (2) ◽  
pp. 559-583 ◽  
Author(s):  
Pavel Kočovský ◽  
Ladislav Kohout ◽  
Václav Černý
Keyword(s):  
Perchloric Acid ◽  
Hydrobromic Acid ◽  
Cyclic Ether ◽  
Cyclic Ethers ◽  
Neighboring Group ◽  
Acid Cleavage ◽  
Neighbouring Group Participation ◽  
Aqueous Perchloric Acid ◽  
The Difference ◽  
Electrophilic Additions

Hypobromous acid action upon the 6,7-unsaturated 19-substituted 5α-cholestans Va-Vc results in the formation of two types of products, the cyclic ethers IX as products of 5(O)n participation of the 19-substituent, and the bromohydrins X. All these compounds are formed from the 6α,7α-bromonium ions Va'-Vc'. Under the same conditions the B-homo-5α-cholestane derivatives VIIa-VIIc afforded solely the cyclic ethers XIV as products of 5(O)n participation of the 19-substituent in the cleavage of the bromonium ions VIIa'-VIIc'. Acid cleavage of the 6α,7α-epoxides VIb and VIc with aqueous perchloric acid or hydrobromic acid gave two types of products, i.e. the cyclic ethers XI and the diols XII or bromohydrines XIII. The cyclic ethers XI arise by 5(O)n participation of the 19-substituent. The B-homo-6α, 7α-epoxide VIIIc on cleavage with aqueous perchloric acid have solely the cyclic ether XVc and by treatment with hydrobromic acid VIIIc afforded the mixture of XVc, as the main product, and of the bromohydrin XVIc. Discussed is the similarity of the bromonium ion cleavage with the fission of the corresponding epoxides, the mechanism of these reactions and the difference in the behaviour of the isomeric olefins Ia-c, IIIa-c, Va-c and VIIa-c and epoxides IIb,c, IVb,c, VIb,c and VIIIb,c. The competition between ambident neighbouring group participation and external nucleophile attack is discussed as well as the dependence of the products ratio on the nucleophilicity of the attacking species.

Substituted N,N-Dimethyl-3-(phenylthio)- and -4-(phenylthio)benzylamines

1992 ◽  
Vol 57 (1) ◽  
pp. 194-203 ◽  
Author(s):  
Karel Šindelář ◽  
Vojtěch Kmoníček ◽  
Marta Hrubantová ◽  
Zdeněk Polívka
Keyword(s):  
Serotonin Receptors ◽  
Hydrobromic Acid ◽  
Antidepressant Activity ◽  
Benzoic Acids ◽  
Lithium Aluminium Hydride ◽  
Acid Chlorides ◽  
Activity Inhibition ◽  
Lithium Aluminium ◽  
The Brain

(Arylthio)benzoic acids IIa - IIe and VIb - VId were transformed via the acid chlorides to the N,N-dimethylamides which were reduced either with diborane "in situ" or with lithium aluminium hydride to N,N-dimethyl-(arylthio)benzylamines Ia - Ie and Vb - Vd. Leuckart reaction of the aldehydes IX and X with dimethylformamide and formic acid afforded directly the amines Va and Ve. Demethylation of the methoxy compounds Ia and Ve with hydrobromic acid resulted in the phenolic amines If and Vf. The most interesting N,N-dimethyl-4-(phenylthio)benzylamine (Va) hydrochloride showed affinity to cholinergic and 5-HT2 serotonin receptors in the rat brain and some properties considered indicative of antidepressant activity (inhibition of serotonin re-uptake in the brain and potentiation of yohimbine toxicity in mice).

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