Face recognition using elastic grid matching through photoshop: A new approach

Directory of Open Access Journals (Sweden)

Manavpreet Kaur

2015-12-01

Full Text Available Computing grids propose to be a very efficacious, economic and ascendable way of image identification. In this paper, we propose a grid based face recognition overture employing a general template matching method to solve the timeconsuming face recognition problem. A new approach has been employed in which the grid was prepared for a specific individual over his photograph using Adobe Photoshop CS5 software. The background was later removed and the grid prepared by merging layers was used as a template for image matching or comparison. This overture is computationally efficient, has high recognition rates and is able to identify a person with minimal efforts and in short time even from photographs taken at different magnifications and from different distances.

Photoshop Elements 12 all-in-one for dummies

CERN Document Server

Obermeier, Barbara

2013-01-01

9 books in 1 Getting Started with ElementsOrganizer FundamentalsImage EssentialsSelectionsPainting, Drawing, and TypingWorking with Layers and MasksFilters, Effects, Styles, and DistortionsRetouching and EnhancingCreating and Sharing with Elements Create extraordinary photos with Photoshop Elements 12 and this friendly guide! These days, we're practically never without a camera at hand - even if it's just a cellphone. Whatever you shoot with, Photoshop Elements can help you make your shots look their best. The nine easy-to-follow minibooks in this guide will help you organize, edit, create, a

Beauty is only photoshop deep: legislating models' BMIs and photoshopping images.

Science.gov (United States)

Krawitz, Marilyn

2014-06-01

Many women struggle with poor body image and eating disorders due, in part, to images of very thin women and photoshopped bodies in the media and advertisements. In 2013, Israel's Act Limiting Weight in the Modelling Industry, 5772-2012, came into effect. Known as the Photoshop Law, it requires all models in Israel who are over 18 years old to have a body mass index of 18.5 or higher. The Israeli government was the first government in the world to legislate on this issue. Australia has a voluntary Code of Conduct that is similar to the Photoshop Law. This article argues that the Australian government should follow Israel's lead and pass a law similar to the Photoshop Law because the Code is not sufficiently binding.

Photoshop CC for dummies

CERN Document Server

Bauer, Peter

2013-01-01

Stretch your creativity beyond the cloud with this fully-updated Photoshop guide!Photoshop puts amazing design and photo-editing tools in the hands of creative professionals and hobbyists everywhere, and the latest version - Photoshop CC - is packed with even more powerful tools to help you manage and enhance your images. This friendly, full-color guide introduces you to the basics of Photoshop CC and provides clear explanations of the menus, panels, tools, options, and shortcuts you'll use the most. Plus, you'll learn valuable tips for fixing common photo flaws, improvin

Adobe Photoshop CC for photographers

CERN Document Server

Evening, Martin

2014-01-01

Adobe Photoshop for Photographers 2014 Release by Photoshop hall-of-famer and acclaimed digital imaging professional Martin Evening has been fully updated to include detailed instruction for all of the updates to Photoshop CC 2014 on Adobe's Creative Cloud, including significant new features, such as Focus Area selections, enhanced Content-Aware filling, and new Spin and Path blur gallery effects. This guide covers all the tools and techniques photographers and professional image editors need to know when using Photoshop, from workflow guidance to core skills to advanced techniques for profess

Photoshop Elements 5 The Missing Manual

CERN Document Server

Brundage, Barbara

2006-01-01

Anyone still think that Adobe Photoshop Elements is a toy version of the real thing? As the most popular photo-editing program on the market, Photoshop Elements not only has Photoshop's marvelous powers, but also has capabilities the mothership lacks. Each new version includes more tools designed specifically for today's consumer digital photo enthusiasts. The latest edition, Photoshop Elements 5, solidifies the reputation of this superb and inexpensive product with new scrapbook features, a link to online photo services, and many other improvements. In fact, there's so much to Photoshop Ele

Photoshop Elements 10 For Dummies

CERN Document Server

Obermeier, Barbara

2011-01-01

Perfect your photos and images with this "focused" guide to the latest version of Photoshop Elements For most of us, the professional-level Photoshop is overkill for our needs. Amateur photographers and photo enthusiasts turn to Photoshop Elements for a powerful but simpler way to edit and retouch their snapshots. Photoshop Elements 10 For Dummies, fully updated and revised for the latest release of this software product, helps you navigate Elements to create, edit, fix, share, and organize the high-quality images you desire. Full color pages bring the techniques to life and make taking great

Technobabble: Photoshop 6 Converges Web, Print Photograph-Editing Capabilities.

Science.gov (United States)

Communication: Journalism Education Today, 2001

2001-01-01

Discusses the newly-released Adobe Photoshop 6, and its use in student publications. Notes its refined text-handling capabilities, a more user-friendly interface, integrated vector functions, easier preparation of Web images, and new and more powerful layer functions. (SR)

Power, speed & automation with Adobe Photoshop

CERN Document Server

Scott, Geoff

2012-01-01

This is a must for the serious Photoshop user! Power, Speed & Automation explores how to customize and automate Photoshop to increase your speed and productivity.  With numerous step-by-step instructions, the authors-two of Adobe's own software developers!- walk you through the steps to best tailor Photoshop's interface to your personal workflow; write and apply Actions; and use batching and scripts to process large numbers of images quickly and automatically.  You will learn how to build your own dialogs and panels to improve your production workflows in Photoshop, the secrets of changing

Enhanced columnar structure in CsI layer by substrate patterning

Energy Technology Data Exchange (ETDEWEB)

Jing, T.; Cho, G.; Drewery, J.; Kaplan, S.N.; Mireshghi, A.; Perez-Mendez, V.; Wildermuth, D. [Lawrence Berkeley Lab., CA (United States); Fujieda, I. [Xerox Palo Alto Research Center, CA (United States)

1991-10-01

Columnar structure in evaporated CsI layers can be controlled by patterning substrates as well as varying evaporation conditions. Mesh-patterned substrates with various dimensions were created by spin-coating polyimide on glass or amorphous silicon substrates and defining patterns with standard photolithography technique. CsI(Tl) layers 200--1000 {mu}m were evaporated. Scintillation properties of these evaporated layers, such as light yield and speed, were equivalent to those of the source materials. Spatial resolution of X-ray detectors consisting of these layers and a linear array of X-ray detectors consisting of these layers and a linear array of Si photodiodes was evaluated by exposing them to a 25{mu}m narrow beam of X-ray. The results obtained with 200{mu}m thick CsI layers coupled to a linear photodiode array with 20 dots/mm resolution showed that the spatial resolution of CsI(Tl) evaporated on patterned substrates was about 75 {mu}m FWHM, whereas that on CsI(Tl) on flat substrates was about 230 {mu}m FWHM. Micrographs taken by SEM revealed that these layers retained the well-defined columnar structure originating from substrate patterns. Adhesion and light transmission of CsI(Tl) were also improved by patterning the substrate.

Teach yourself visually Photoshop CC

CERN Document Server

Wooldridge, Mike

2013-01-01

Get savvy with the newest features and enhancements of Photoshop CC The newest version of Photoshop boasts enhanced and new features that afford you some amazing and creative ways to create images with impact, and this popular guide gets visual learners up to speed quickly. Packed with colorful screen shots that illustrate the step-by-step instructions, this visual guide is perfect for Photoshop newcomers as well as experienced users who are looking for some beginning to intermediate-level techniques to give their projects the ""wow"" factor! Veteran and bestselling authors Mik

Adobe Photoshop CC for photographers a professional image editor's guide to the creative use of Photoshop for the Macintosh and PC

CERN Document Server

Evening, Martin

2013-01-01

Martin Evening, Photoshop hall-of-famer and acclaimed digital imaging professional, has revamped his much-admired Photoshop for Photographers book for an eleventh edition, to include detailed instruction for all of the updates to Photoshop CC on Adobe's Creative Cloud. This comprehensive guide covers all the tools and techniques serious photographers need to know when using Photoshop, from workflow guidance to core skills to advanced techniques for professional results. Using clear, succinct instruction and real world examples, this guide is the essential reference for Photoshop users of al

The clinical application of Photoshop in image post-processing of no-gap-lower-limb digital photography

International Nuclear Information System (INIS)

Zhang Ziqi; Wang Longhua; Feng Min; Gu Jianping; Lu Lingquan; Gui Jianchao; Wang Liming

2006-01-01

Objective: To explore the value of Photoshop in image post-processing of digital total lower-limb X-ray photography, so as to obtain a more reasonable and accurate photography. Methods: Digital total lower-limb X-ray photography was performed in 34 patients, and the films were printed. Then the digital imaging were converted to a total no-gap-tower-limb photography by Adobe Photoshop CS software and were printed in A4 sheets. The Q angles ( the angle between the line of femoral axis and the line of central points of femoral head, knee joint and ankle joint) were measured by radiologists and orthopedists. The films and pages were evaluated separately by radiologists and orthopedists. The Q angles were compared. Results: There were 25 cases retrograde osteoarthritis of knee joints inl9 patients (6 patients were involved two sides), 15 cases of rheumatoid osteoarthritis in 12 patients, 1 case of malformation, 1 case of traumatic osteoarthritis, and 1 case of TB. Twenty-six of these patients were performed the knee joint replacement operations. The Q angle in films were (6.3±0.8) degree, and (6.1±0.3) degree in sheets. There was no significant difference between the two methods (paired-t-test, t=0.022, P>0.5). Conclusion: Photoshop software could be used readily to obtain a optional total no-gap-lower limb photography satisfying diagnostic and operational needs of orthopedics. (authors)

Photoshop Elements 10 All-in-One For Dummies

CERN Document Server

Obermeier, Barbara

2011-01-01

Create your photo vision with the latest version of Photoshop Elements Photoshop Elements is the top selling consumer photo editing software and Adobe continues to add innovative features that allow digital photo enthusiasts to do it all. This value-packed reference combines nine content-rich minibooks in one complete package. User-friendly and detailed, it covers the key features and tools that beginner and experienced users need to create high-quality images for print, e-mail, and the web using the latest release of Photoshop Elements - Photoshop Elements 10. Presented in full color, this re

Clean Up Your Image: A Beginner's Guide to Scanning and Photoshop

Science.gov (United States)

Stitzer, Michael S.

2005-01-01

In this article, the author addresses the key steps of scanning and illustrates the process with screen shots taken from a Macintosh G4 Powerbook computer running OSX and Adobe Photoshop 7.0. After reviewing scanning procedures, the author describes how to use Photoshop 7.0 to manipulate a scanned image. This activity gives students a good general…

Photoshop CC top 100 simplified tips and tricks

CERN Document Server

Sholik, Stan

2013-01-01

Take your Photoshop skill set to the next level with these essential techniques If you're already familiar with Photoshop basics and are ready to learn some new tips, tricks, and techniques, then this is the book for you! Full-color, step-by-step instructions take you beyond the essentials and show you how to make the most of the newest features of Photoshop CC (Creative Cloud). Beautiful photos will inspire you to experiment with Photoshop's features, and numbered instructions make the techniques easy to learn. Encourages you to expand your skill set with creative, or

PTX-loaded three-layer PLGA/CS/ALG nanoparticle based on layer-by-layer method for cancer therapy.

Science.gov (United States)

Wang, Fang; Yuan, Jian; Zhang, Qian; Yang, Siqian; Jiang, Shaohua; Huang, Chaobo

2018-05-17

Poly (lactic-co-glycolic acid) (PLGA) nanoparticles are an ideal paclitaxel (PTX)-carrying system due to its biocompatibility and biodegradability. But it possessed disadvantage of drug burst release. In this research, a layer-by-layer deposition of chitosan (CS) and sodium alginate (ALG) was applied to modify the PLGA nanoparticles. The surface charges and morphology of the PLGA, PLGA/CS and PLGA/CS/ALG particles was measured by capillary electrophoresis and SEM and TEM, respectively. The drug encapsulation and loading efficiency were confirmed by ultraviolet spectrophotometer. The nanoparticles were stable and exhibited controlled drug release performance, with good cytotoxicity to human lung carcinoma cells (HepG 2). Cumulatively, our research suggests that this kind of three-layer nanoparticle with LbL-coated shield has great properties to act as a novel drug-loaded system.

Energy- and temperature dependences of secondary electron emission of CsI- and CsBr layers doped with Cd

International Nuclear Information System (INIS)

Galij, P.V.; Tsal', N.A.

1983-01-01

The energy and temperature dependences of the secondary electron emission coefficient (SEEC) of CsI-Cd-, CsBr-Cd-, CsI-CsBr layers have been studied. The effect of bivalent cadmium impurity on the SEEC value is investigated. It is shown that implantation of small amounts of Cd 2+ impurity into the lattice of the initial monocrystals might increase the SEEC values of the layers. Temperature dependences (TD) of SEEC are measured and the possibility of comparing experimental results with the Dekker formula is analyzed. A conclusion is drawn that the Dekker model well describes the TD of SEEC of doped layers at temperatures T < or approximately 100 deg C. At elevated temperatures., along with secondary electron scattering on phonons, one should take into account their scattering on vacancies

Measurement of facial movements with Photoshop software during treatment of facial nerve palsy*

Science.gov (United States)

Pourmomeny, Abbas Ali; Zadmehr, Hassan; Hossaini, Mohsen

2011-01-01

BACKGROUND: Evaluating the function of facial nerve is essential in order to determine the influences of various treatment methods. The aim of this study was to evaluate and assess the agreement of Photoshop scaling system versus the facial grading system (FGS). METHODS: In this semi-experimental study, thirty subjects with facial nerve paralysis were recruited. The evaluation of all patients before and after the treatment was performed by FGS and Photoshop measurements. RESULTS: The mean values of FGS before and after the treatment were 35 ± 25 and 67 ± 24, respectively (p Photoshop assessment, mean changes of face expressions in the impaired side relative to the normal side in rest position and three main movements of the face were 3.4 ± 0.55 and 4.04 ± 0.49 millimeter before and after the treatment, respectively (p Photoshop was more objective than using FGS. Therefore, it may be recommended to use this method instead. PMID:22973325

Measurement of facial movements with Photoshop software during treatment of facial nerve palsy.

Science.gov (United States)

Pourmomeny, Abbas Ali; Zadmehr, Hassan; Hossaini, Mohsen

2011-10-01

Evaluating the function of facial nerve is essential in order to determine the influences of various treatment methods. The aim of this study was to evaluate and assess the agreement of Photoshop scaling system versus the facial grading system (FGS). In this semi-experimental study, thirty subjects with facial nerve paralysis were recruited. The evaluation of all patients before and after the treatment was performed by FGS and Photoshop measurements. The mean values of FGS before and after the treatment were 35 ± 25 and 67 ± 24, respectively (p Photoshop assessment, mean changes of face expressions in the impaired side relative to the normal side in rest position and three main movements of the face were 3.4 ± 0.55 and 4.04 ± 0.49 millimeter before and after the treatment, respectively (p Photoshop was more objective than using FGS. Therefore, it may be recommended to use this method instead.

The Photoshop Darkroom 2 creative digital transformations

CERN Document Server

Davis, Harold

2011-01-01

Award-winning photography/design team Harold and Phyllis Davis are back with a brand new volume in their new Photoshop Darkroom series. Picking up where their best-selling first book left off, The Photoshop Darkroom 2: Advanced Digital Post-Processing will show you everything you need to know to take your digital imaging skills to the next level. Great photographers know that the best images begin well before the shutter clicks, and certainly well before Photoshop boots up. Harold takes a step back, and shares his helpful tips for capturing the most compelling images possible by keeping in min

Appling Andragogy Theory in Photoshop Training Programs

Science.gov (United States)

Alajlan, Abdulrahman Saad

2015-01-01

Andragogy is a strategy for teaching adults that can be applied to Photoshop training. Photoshop workshops are frequented by adult learners, and thus andragogical models for instruction would be extremely helpful for prospective trainers looking to improve their classroom designs. Adult learners are much different than child learners, given the…

Synthesis and crystal structure of the cesium silver permanganate Cs_3Ag[MnO_4]_4

International Nuclear Information System (INIS)

Bauchert, Joerg M.; Henning, Harald; Schleid, Thomas

2012-01-01

After successful syntheses and structural refinements of the already known permanganates of cesium (Cs[MnO_4]) and silver (Ag[MnO_4]) we started to blend aqueous solutions of both components in various molar ratios. From crystallization experiments of these mixtures only three species of crystals with different chemical compositions were obtained: tricesium monosilver tetrakispermanganate (Cs_3Ag[MnO_4]_4) and, depending upon the respective ratio, either additional silver permanganate or surplus cesium permanganate, namely. The new title compound crystallizes in the orthorhombic space group Pnnm (no. 58) with two formula units per unit cell and cell dimensions of a = 764.53(4), b = 1883.57(9) and c = 584.34(3) pm. The crystal structure of Cs_3Ag[MnO_4]_4 consists of two crystallographically distinguishable cesium cations. (Cs1)"+ is surrounded by fourteen oxygen atoms constructing a slightly distorted bicapped hexagonal prism. These polyhedra are connected through edge-sharing with two other polyhedra of this kind to form chains along [001]. The chains are linked to each other via sixfold coordinated Ag"+ cations (d(Ag-O) = 238-246 pm), arranged in such a manner that they link three oxygen atoms of two cesium polyhedra, leading to a two-dimensional layer spreading out parallel to the (001) plane. Together with the two crystallographically different tetrahedral oxomanganate(VII) anions [MnO_4]"- (d(Mn-O) = 161-162 pm) the other kind of cesium cations ((Cs2)"+ with CN = 13) finally connect these layers three-dimensionally. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Geometrical verification system using Adobe Photoshop in radiotherapy.

Science.gov (United States)

Ishiyama, Hiromichi; Suzuki, Koji; Niino, Keiji; Hosoya, Takaaki; Hayakawa, Kazushige

2005-02-01

Adobe Photoshop is used worldwide and is useful for comparing portal films with simulation films. It is possible to scan images and then view them simultaneously with this software. The purpose of this study was to assess the accuracy of a geometrical verification system using Adobe Photoshop. We prepared the following two conditions for verification. Under one condition, films were hanged on light boxes, and examiners measured distances between the isocenter on simulation films and that on portal films by adjusting the bony structures. Under the other condition, films were scanned into a computer and displayed using Adobe Photoshop, and examiners measured distances between the isocenter on simulation films and those on portal films by adjusting the bony structures. To obtain control data, lead balls were used as a fiducial point for matching the films accurately. The errors, defined as the differences between the control data and the measurement data, were assessed. Errors of the data obtained using Adobe Photoshop were significantly smaller than those of the data obtained from films on light boxes (p Adobe Photoshop is available on any PC with this software and is useful for improving the accuracy of verification.

Focus On Adobe Photoshop Focus on the Fundamentals

CERN Document Server

Hilz, Corey

2011-01-01

This no-nonsense, highly affordable, and inspiring guide walks photographers new to Photoshop through the end to end Photoshop workflow. Starting from the moment you download your images off your memory card, photographer Corey Hilz guides you through importing and organizing your photos in Bridge, demonstrating how to give each photo ratings and keywords to make searching through your photos a snap. He then details the basics of editing photos in both Camera Raw and Photoshop, including how to correct exposure, make color and tonal adjustments, retouch flaws and imperfections, and much more.

Structural Series in the Ternary A-Mn-As System (A = Alkali Metal): Double-Layer-Type CsMn4As3 and RbMn4As3 and Tunnel-Type KMn4As3.

Science.gov (United States)

Ishida, Junichi; Iimura, Soshi; Hosono, Hideo

2018-04-16

New manganese arsenides CsMn 4 As 3 , RbMn 4 As 3 , and KMn 4 As 3 were synthesized by solid-state reaction. They consist of edge-sharing MnAs 4 tetrahedra, which are a building block similar to those of Fe-based superconductors. CsMn 4 As 3 and RbMn 4 As 3 adopt the KCu 4 S 3 -type structure (tetragonal P4/ mmm space group, No. 123) with a Mn 4 As 3 double layer, while KMn 4 As 3 has the CaFe 4 As 3 -type structure (orthorhombic Pnma space group, No. 62) with a Mn 4 As 3 tunnel framework. The structural change from CsMn 4 As 3 and RbMn 4 As 3 to KMn 4 As 3 as well as the structural trend of the other ternary A-Mn-As (A = alkali metal) and AE-Mn-As (AE = alkaline-earth metal) compounds is understood as a consequence of reduction of the coordination number around the A and AE sites owing to the decrease of the ionic radius from Cs + to Mg 2+ . Electrical resistivity measurements confirm that the three new phases are Mott insulators with band gaps of 0.52 (CsMn 4 As 3 ), 0.43 (RbMn 4 As 3 ), and 0.31 eV (KMn 4 As 3 ). Magnetic and heat capacity measurements revealed that CsMn 4 As 3 and RbMn 4 As 3 are antiferromagnets without apparent phase transitions below 400 K, which is similar to the magnetism of LaMnAsO and BaMn 2 As 2 , while the existence of the ferromagnetic component was indicated in KMn 4 As 3 with a magnetic transition at 179 K.

Focus On Photoshop Elements Focus on the Fundamentals

CERN Document Server

Asch, David

2011-01-01

Are you bewildered by the advanced editing options available in Photoshop Elements? Do you want to get the most out of your image without going bleary-eyed in front of a computer screen? This handy guide will explain the ins and outs of using Photoshop Elements, without having to spend hours staring at the screen. Using a fabulous combination of easy-to-follow advice and step-by-step instructions, Focus On Photoshop Elements gives great advice on setting up, storing and sharing your image library and teaches you the basics of RAW image processing and color correction, plus shows you how to edi

Layer-by-layer deposition of nanostructured CsPbBr3 perovskite thin films

Science.gov (United States)

Reshetnikova, A. A.; Matyushkin, L. B.; Andronov, A. A.; Sokolov, V. S.; Aleksandrova, O. A.; Moshnikov, V. A.

2017-11-01

Layer-by-layer deposition of nanostructured perovskites cesium lead halide thin films is described. The method of deposition is based on alternate immersion of the substrate in the precursor solutions or colloidal solution of nanocrystals and methyl acetate/lead nitrate solution using the device for deposition of films by SILAR and dip-coating techniques. An example of obtaining a photosensitive structure based on nanostructures of ZnO nanowires and layers of CsBbBr3 nanocrystals is also shown.

Photoshop Elements 10 Top 100 Simplified Tips and Tricks

CERN Document Server

Sheppard, Rob

2011-01-01

A visual guide to getting the most out of Photoshop Elements 10 If you understand the basics of Photoshop Elements, you'll love this collection of 100 must-know tips and tricks. Two-page tutorials, full-color screen shots, and step-by-step instructions make it easy to see and follow the directions, helping you to get the very most from this top-selling image-editing software. This guide catches you up on Photoshop Elements 10, covers features you may not have known about, and alerts you to a slew of cool effects and techniques. Explains techniques, best practices, and creative ways to transfor

Thermal gravimetric analysis of the CsCuCl3, Cs2CuCl4 and Cs2CuCl4x2H2O crystals

International Nuclear Information System (INIS)

Soboleva, L.V.; Vasil'eva, M.G.

1977-01-01

The thermal characteristics of crystals of Cs 2 CuCl 4 , Cs 2 CuCl 4 x2H 2 O, and CsCuCl 3 were investigated thermogravimetrically. The derivatogram of the Cs 2 CuCl 4 crystal is characterized by the presence of a single endothermal effect at 505 deg C. The derivatogram of the Cs 2 CuCl 4 x2H 2 O crystal contains three endothermal effects: at 40, 135, and 480 deg C. The derivatogram of the CsCuCl 3 crystal shows the presence of two endothermal effects at 142 and 455 deg C. The thermogravimetric data on Cs 2 CuCl 4 and CsCuCl 3 crystals reveal crystal decomposition on melting; hence, these crystals cannot be grown from melts

Imbedded Nanocrystals of CsPbBr3 in Cs4 PbBr6 : Kinetics, Enhanced Oscillator Strength, and Application in Light-Emitting Diodes.

Science.gov (United States)

Xu, Junwei; Huang, Wenxiao; Li, Peiyun; Onken, Drew R; Dun, Chaochao; Guo, Yang; Ucer, Kamil B; Lu, Chang; Wang, Hongzhi; Geyer, Scott M; Williams, Richard T; Carroll, David L

2017-11-01

Solution-grown films of CsPbBr 3 nanocrystals imbedded in Cs 4 PbBr 6 are incorporated as the recombination layer in light-emitting diode (LED) structures. The kinetics at high carrier density of pure (extended) CsPbBr 3 and the nanoinclusion composite are measured and analyzed, indicating second-order kinetics in extended and mainly first-order kinetics in the confined CsPbBr 3 , respectively. Analysis of absorption strength of this all-perovskite, all-inorganic imbedded nanocrystal composite relative to pure CsPbBr 3 indicates enhanced oscillator strength consistent with earlier published attribution of the sub-nanosecond exciton radiative lifetime in nanoprecipitates of CsPbBr 3 in melt-grown CsBr host crystals and CsPbBr 3 evaporated films. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Teach yourself visually Photoshop Elements 12

CERN Document Server

Wooldridge, Mike

2013-01-01

Are you a visual learner? Do you prefer instructions that show you how to do something - and skip the long-winded explanations? If so, then this book is for you. Open it up and you'll find clear, step-by-step screen shots that show you how to tackle more than 160 Photoshop Elements tasks. Each task-based spread covers a single technique, sure to help you get up and running on Photoshop Elements 12 in no time. You'll learn to:Use both the Organizer and EditorImport photos from various sourcesEnhance lighting and colorRestore old photos and add effectsSave, back up, and share photos Designed f

Synthesis and crystal structure of the cesium silver permanganate Cs{sub 3}Ag[MnO{sub 4}]{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Bauchert, Joerg M.; Henning, Harald; Schleid, Thomas [Institut fuer Anorganische Chemie, Universitaet Stuttgart (Germany)

2012-09-15

After successful syntheses and structural refinements of the already known permanganates of cesium (Cs[MnO{sub 4}]) and silver (Ag[MnO{sub 4}]) we started to blend aqueous solutions of both components in various molar ratios. From crystallization experiments of these mixtures only three species of crystals with different chemical compositions were obtained: tricesium monosilver tetrakispermanganate (Cs{sub 3}Ag[MnO{sub 4}]{sub 4}) and, depending upon the respective ratio, either additional silver permanganate or surplus cesium permanganate, namely. The new title compound crystallizes in the orthorhombic space group Pnnm (no. 58) with two formula units per unit cell and cell dimensions of a = 764.53(4), b = 1883.57(9) and c = 584.34(3) pm. The crystal structure of Cs{sub 3}Ag[MnO{sub 4}]{sub 4} consists of two crystallographically distinguishable cesium cations. (Cs1){sup +} is surrounded by fourteen oxygen atoms constructing a slightly distorted bicapped hexagonal prism. These polyhedra are connected through edge-sharing with two other polyhedra of this kind to form chains along [001]. The chains are linked to each other via sixfold coordinated Ag{sup +} cations (d(Ag-O) = 238-246 pm), arranged in such a manner that they link three oxygen atoms of two cesium polyhedra, leading to a two-dimensional layer spreading out parallel to the (001) plane. Together with the two crystallographically different tetrahedral oxomanganate(VII) anions [MnO{sub 4}]{sup -} (d(Mn-O) = 161-162 pm) the other kind of cesium cations ((Cs2){sup +} with CN = 13) finally connect these layers three-dimensionally. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

How to cheat in Photoshop Elements 12 release your imagination

CERN Document Server

Asch, David

2014-01-01

Have you ever wanted to summon magical powers? Appear in a graphic novel? Or control the weather and seasons? There's a whole world of opportunity out there for creating fun photomontages, powerful panoramas, and dynamic distortions.How to Cheat in Photoshop Elements 12 starts you at the basics of photomontage with selection techniques, layers and transformations; leading up to full-length projects for creating magazine covers, fantasy scenes, poster artwork and much, much more.This book also features:A dedicated website where you can download images and tutorial videos that show you how to ex

Dielectric barrier discharge image processing by Photoshop

Science.gov (United States)

Dong, Lifang; Li, Xuechen; Yin, Zengqian; Zhang, Qingli

2001-09-01

In this paper, the filamentary pattern of dielectric barrier discharge has been processed by using Photoshop, the coordinates of each filament can also be obtained. By using Photoshop two different ways have been used to analyze the spatial order of the pattern formation in dielectric barrier discharge. The results show that the distance of the neighbor filaments at U equals 14 kV and d equals 0.9 mm is about 1.8 mm. In the scope of the experimental error, the results from the two different methods are similar.

Syntheses, crystal structure, and electronic properties of the five ABaMQ{sub 4} compounds RbBaPS{sub 4}, CsBaPS{sub 4}, CsBaVS{sub 4}, RbBaVSe{sub 4}, and CsBaVSe{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Mesbah, Adel [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States); ICSM, UMR 5257 CEA / CNRS / UM / ENSCM, Site de Marcoule-Bâtiment 426, BP 17171, 30207 Bagnols-sur-Cèze Cedex (France); Prakash, Jai [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States); Rocca, Dario; Lebègue, Sébastien [Laboratoire de Cristallographie, Résonance Magnétique, et Modélisations CRM2 (UMR UHP-CNRS 7036), Faculté des Sciences et Techniques, Université de Lorraine, BP 70239, Boulevard des Aiguillettes, 54506 Vandoeuvre-lès-Nancy Cedex (France); Beard, Jessica C.; Lewis, Benjamin A. [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States); Ibers, James A., E-mail: ibers@chem.northwestern.edu [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States)

2016-01-15

Five new compounds belonging to the ABaMQ{sub 4} family were synthesized by solid-state chemistry at 1123 K. The compounds RbBaPS{sub 4}, CsBaPS{sub 4}, CsBaVS{sub 4}, RbBaVSe{sub 4}, and CsBaVSe{sub 4} are isostructural and have the TlEuPS{sub 4} structure type. They crystallize in space group D{sup 16}{sub 2h} – Pnma of the orthorhombic system. Their structure consists isolated MQ{sub 4} tetrahedra separated by A and Ba atoms to form a salt-like structure. Density Functional Theory (DFT) calculations of the electronic structures with the use of the HSE functional suggest that the compounds are semiconductors with calculated band gaps of 3.3 eV (RbBaPS{sub 4}), 3.4 eV (CsBaPS{sub 4}), 2.3 eV (CsBaVS{sub 4}), and 1.6 eV (RbBaVSe{sub 4}). - Graphical abstract: General view of the ABaMQ{sub 4} structure down the a axis. - Highlights: • Five new ABaMQ{sub 4} compounds were synthesized by solid-state chemistry at 1123 K. • RbBaPS{sub 4}, CsBaPS{sub 4}, CsBaVS{sub 4}, RbBaVSe{sub 4}, and CsBaVSe{sub 4} have the TlEuPS{sub 4} structure type. • The compounds are semiconductors with calculated band gaps ranging from 1.6 to 3.4 eV.

[APPLICATION OF PHOTOSHOP CS16.0 SOFTWARE IN PREOPERATIVE OSTEOTOMY DESIGN OF ANKYLOSING SPONDYLITIS KYPHOSIS].

Science.gov (United States)

Wang, Fei; Tao, Huiren; Liu, Zhibin; Zhang, Jianhua; Han, Fangmin

2015-02-01

To introduce the application of Photoshop CS16.0 (PS) software in preoperative osteotomy design of ankylosing spondylitis kyphosis (ASK), and to investigate applied values of the preoperative design. Between March 2009 and March 2013, 21 cases of ASK were treated through preoperative osteotomy design by using PS software. There were 16 males and 5 females, aged from 23 to 50 years (mean, 34.2 years). The deformity included thoracolumbar kyphosis in 14 cases, thoracic kyphosis in 2 cases, and lumbar kyphosis in 5 cases. The ultimate osteotomy angle of preoperative plans and the location and extent of osteotomy were determined by the osteotomy design, which guided operation procedures of the surgeon. The actual osteotomy angle was obtained by measuring Cobb angle of osteotomy segment before and after operation. The sagittal parameters of spine and pelvis including global kyphosis (GK), lumbar lordosis (LL), sagittal vertical axis (SVA), pelvic incidence (PI), pelvic tilt (PT), and chin brow-vertical angle (CBVA) were measured at preoperation, at 1 week after operation, and last follow-up. The clinical outcomes were assessed by simplified Chinese Scoliosis Research Society-22 (SRS-22) questionnaire and Oswestry disability index (ODI). No complications occurred in the other cases except 1 case of dural tear during operation and 1 case of nerve injury after operation, and primary healing of incision was obtained. All patients were followed up 14 to 45 months (mean, 26.3 months). The SRS-22 and ODI scores at 1 week after operation and last follow-up were significantly improved when compared with preoperative scores (P 0.05). The preoperative planned osteotomy angle and the postoperative actual osteotomy angle were (34.2 ± 10.5) degrees and (33.7 ± 9.7) degrees respectively, showing no significant difference (t = 0.84, P = 0.42). The CBVA, GK, SVA, PT, and LL were significantly improved when compared with the preoperative values (P 0.05). At last follow-up, no failures

Enhancing Hybrid Perovskite Detectability in the Deep Ultraviolet Region with Down-Conversion Dual-Phase (CsPbBr3-Cs4PbBr6) Films.

Science.gov (United States)

Tong, Guoqing; Li, Huan; Zhu, Zhifeng; Zhang, Yan; Yu, Linwei; Xu, Jun; Jiang, Yang

2018-04-05

Hybrid perovskite photodetectors (PDs) exhibit outstanding performance in the ultraviolet-visible (UV-vis) spectrum but have poor detectability in the deep ultraviolet (DUV) region (200-350 nm). In this work, a novel inorganic-hybrid architecture that incorporates a dual-phase (CsPbBr 3 -Cs 4 PbBr 6 ) inorganic perovskite material as a down-conversion window layer and a hybrid perovskite as a light capture layer was prepared to achieve faster, highly sensitive photodetection in the DUV spectrum. A dual-phase inorganic perovskite film coated on the back surface of the photodetector enables strong light absorption and tunes the incident energy into emission bands that are optimized for the perovskite photodetector. The presence of Cs 4 PbBr 6 enhances the capture and down-conversion of the incident DUV light. Due to the down-conversion and transport of the DUV photons, a self-driven perovskite photodetector with this composite structure exhibits a fast response time of 7.8/33.6 μs and a high responsivity of 49.4 mA W -1 at 254 nm without extra power supply.

Software Aids for radiologists: Part 1, Useful Photoshop skills.

Science.gov (United States)

Gross, Joel A; Thapa, Mahesh M

2012-12-01

The purpose of this review is to describe the use of several essential techniques and tools in Adobe Photoshop image-editing software. The techniques shown expand on those previously described in the radiologic literature. Radiologists, especially those with minimal experience with image-editing software, can quickly apply a few essential Photoshop tools to minimize the frustration that can result from attempting to navigate a complex user interface.

Bodyshop The PhotoShop Retouching Guide for the Face and Body

CERN Document Server

Nitzsche, Birgit

2011-01-01

The book Photoshop users need to get bodies into shape.This full-color book will show how both the newest and previous versions of Photoshop can be used to retouch and enhance the entire human form.From body contouring to changing hairstyles to adding makeup and fixing nails, this book will be a must-have reference for anyone who uses Photoshop to fix people pictures.The companion DVD includes before-and-after views of all pictures from the book, additional setting files for individual workshops, and trial versions of several Nik Multimedia filters.

Hybridization of Single Nanocrystals of Cs4PbBr6 and CsPbBr3.

Science.gov (United States)

Weerd, Chris de; Lin, Junhao; Gomez, Leyre; Fujiwara, Yasufumi; Suenaga, Kazutomo; Gregorkiewicz, Tom

2017-09-07

Nanocrystals of all-inorganic cesium lead halide perovskites (CsPbX 3 , X = Cl, Br, I) feature high absorption and efficient narrow-band emission which renders them promising for future generation of photovoltaic and optoelectronic devices. Colloidal ensembles of these nanocrystals can be conveniently prepared by chemical synthesis. However, in the case of CsPbBr 3 , its synthesis can also yield nanocrystals of Cs 4 PbBr 6 and the properties of the two are easily confused. Here, we investigate in detail the optical characteristics of simultaneously synthesized green-emitting CsPbBr 3 and insulating Cs 4 PbBr 6 nanocrystals. We demonstrate that, in this case, the two materials inevitably hybridize, forming nanoparticles with a spherical shape. The actual amount of these Cs 4 PbBr 6 nanocrystals and nanohybrids increases for synthesis at lower temperatures, i.e., the condition typically used for the development of perovskite CsPbBr 3 nanocrystals with smaller sizes. We use state-of-the-art electron energy loss spectroscopy to characterize nanoparticles at the single object level. This method allows distinguishing between optical characteristics of a pure Cs 4 PbBr 6 and CsPbBr 3 nanocrystal and their nanohybrid. In this way, we resolve some of the recent misconceptions concerning possible visible absorption and emission of Cs 4 PbBr 6 . Our method provides detailed structural characterization, and combined with modeling, we conclusively identify the nanospheres as CsPbBr 3 /Cs 4 PbBr 6 hybrids. We show that the two phases are independent of each other's presence and merge symbiotically. Herein, the optical characteristics of the parent materials are preserved, allowing for an increased absorption in the UV due to Cs 4 PbBr 6 , accompanied by the distinctive efficient green emission resulting from CsPbBr 3 .

[Energy pooling collisions for K(4P) + Cs(5D) in a K-Cs mixture].

Science.gov (United States)

Aihemaiti, Pulati; Dai, Kang; Lu, Xin-hong; Shen, Yi-fan

2005-04-01

The rate coefficients for energy-pooling collisions K(4P) + Cs(5D) --> Cs(6S) + K(4D, 6S) in the K-Cs vapor mixture were measured relative to a known energy-pooling rate coefficient of a homonuclear reaction [i. e., Cs(6P) + Cs(5D) --> Cs(6S) + Cs (7D(J))]. Populations of the Cs(6P, 5D) and K(4P) states were produced by photodissociation of K2 and Cs2 molecules through the use of a dye laser radiation. The resulting fluorescence included the direct components emitted in the decay of the excited states produced by photodissociation and the induced components arising from the collisionally populated states. By combining relative intensities of the components with the effective lifetimes of Cs(6P) and K(4P) states, the rate coefficients (in units of 10(-9) cm3 x s(-1)) for the heteronuclear energy-pooling were found to be 2.6 and 3.6, respectively. The contribution to the rate coefficients from other processes are discussed.

On thermal expansion of RbD2PO4, CsH2PO4 and CsDrPO4 crystals

International Nuclear Information System (INIS)

Vlokh, O.G.; Shchur, Ya.I.; Klymiv, I.M.

1994-01-01

Thermal expansion of RbD 2 PO 4 , CsH 2 PO 4 , CsD 2 PO 4 crystals in a wide range of temperatures embracing points of phase transitions was studied. An explanation of anomalous behaviour of thermal expansion factor along directions b and c in the course of RbD 2 PO 4 transfer into intermediate phase was suggested. 10 refs., 4 figs

Syntheses, crystal structures and photoluminescence properties of two rare-earth molybdates CsLn(MoO{sub 4}){sub 2} (Ln=Eu, Tb)

Energy Technology Data Exchange (ETDEWEB)

Zhao, Dan; Ma, Fa-Xue; Liu, Bao-Zhong; Fan, Yun-Chang; Han, Xue-Feng; Zhang, Lei; Nie, Cong-Kui [Henan Polytechnic Univ. (China). College of Chemistry and Chemical Engineering

2018-04-01

Single crystals of two cesium rare-earth molybdates CsLn(MoO{sub 4}){sub 2} (Ln=Eu, Tb) have been prepared using the high temperature molten salt (flux) method. Single-crystal X-ray diffraction analyses reveal that they crystallize in the orthorhombic space group Pccm (No. 49) and features a 2D layer structure that is composed of [Ln(MoO{sub 4}){sub 2}]{sub ∞} and [Cs]{sub ∞} layers. Under near-UV light excitation, emission spectrum of CsEu(MoO{sub 4}){sub 2} consists of several sharp lines due to the characteristic electronic transitions of Eu{sup 3+} ions, whereas CsTb(MoO{sub 4}){sub 2} exhibits characteristic green emission of Tb{sup 3+} ions.

Learning Flash CS4 Professional

CERN Document Server

Shupe, Rich

2009-01-01

Learning Flash CS4 Professional offers beginners and intermediate Flash developers a unique introduction to the latest version of Adobe's powerful multimedia application. This easy-to-read book is loaded with full-color examples and hands-on tasks to help you master Flash CS4's new motion editor, integrated 3D system, and character control using the new inverse kinematics bones animation system. No previous Flash experience is necessary.

Exploring Polaronic, Excitonic Structures and Luminescence in Cs4PbBr6/CsPbBr3.

Science.gov (United States)

Kang, Byungkyun; Biswas, Koushik

2018-02-15

Among the important family of halide perovskites, one particular case of all-inorganic, 0-D Cs 4 PbBr 6 and 3-D CsPbBr 3 -based nanostructures and thin films is witnessing intense activity due to ultrafast luminescence with high quantum yield. To understand their emissive behavior, we use hybrid density functional calculations to first compare the ground-state electronic structure of the two prospective compounds. The dispersive band edges of CsPbBr 3 do not support self-trapped carriers, which agrees with reports of weak exciton binding energy and high photocurrent. The larger gap 0-D material Cs 4 PbBr 6 , however, reveals polaronic and excitonic features. We show that those lattice-coupled carriers are likely responsible for observed ultraviolet emission around ∼375 nm, reported in bulk Cs 4 PbBr 6 and Cs 4 PbBr 6 /CsPbBr 3 composites. Ionization potential calculations and estimates of type-I band alignment support the notion of quantum confinement leading to fast, green emission from CsPbBr 3 nanostructures embedded in Cs 4 PbBr 6 .

Tunable CsPbBr3/Cs4PbBr6 phase transformation and their optical spectroscopic properties.

Science.gov (United States)

Chen, Xiao; Chen, Daqin; Li, Junni; Fang, Gaoliang; Sheng, Hongchao; Zhong, Jiasong

2018-04-24

As a novel type of promising materials, metal halide perovskites are a rising star in the field of optoelectronics. On this basis, a new frontier of zero-dimensional perovskite-related Cs4PbBr6 with bright green emission and high stability has attracted an enormous amount of attention, even though its photoluminescence still requires to clarification. Herein, the controllable phase transformation between three-dimensional CsPbBr3 and zero-dimensional Cs4PbBr6 is easily achieved in a facile ligand-assisted supersaturated recrystallization synthesis procedure via tuning the amount of surfactants, and their unique optical properties are investigated and compared in detail. Both Cs4PbBr6 and CsPbBr3 produce remarkably intense green luminescence with quantum yields up to 45% and 80%, respectively; however, significantly different emitting behaviors are observed. The fluorescence lifetime of Cs4PbBr6 is much longer than that of CsPbBr3, and photo-blinking is easily detected in the Cs4PbBr6 product, proving that the zero-dimensional Cs4PbBr6 is indeed a highly luminescent perovskite-related material. Additionally, for the first time, tunable emissions over the visible-light spectral region are demonstrated to be achievable via halogen composition modulations in the Cs4PbX6 (X = Cl, Br, I) samples. Our study brings a simple method for the phase control of CsPbBr3/Cs4PbBr6 and demonstrates the intrinsic luminescence nature of the zero-dimensional perovskite-related Cs4PbX6 products.

Sr2+ and Cs+ ion exchange properties of KLn(PO3)4: Ln = Ce and Eu

International Nuclear Information System (INIS)

Samatha, B.; Achary, S.N.; Tyagi, A.K.; Ramkumar, Jayshree; Chandramouleeswaran, S.

2014-01-01

With the aim to study the potential of layered phosphates as ion exchangers two stoichiometric compositions as KLn(PO 3 ) 4 with Ln = Ce and Eu were prepared by solid state reaction and characterized by powder X-ray diffraction method. The Cs + and Sr 2+ exchange properties of both materials were investigated using standard solutions of Sr 2 + or Cs + in low acidic aqueous medium

Two-gap superconductivity with line nodes in CsCa2Fe4As4F2

Science.gov (United States)

Kirschner, Franziska K. K.; Adroja, Devashibhai T.; Wang, Zhi-Cheng; Lang, Franz; Smidman, Michael; Baker, Peter J.; Cao, Guang-Han; Blundell, Stephen J.

2018-02-01

We report the results of a muon-spin rotation (μ SR ) experiment to determine the superconducting ground state of the iron-based superconductor CsCa2Fe4As4F2 with Tc≈28.3 K . This compound is related to the fully gapped superconductor CaCsFe4As4 , but here the Ca-containing spacer layer is replaced with one containing Ca2F2 . The temperature evolution of the penetration depth strongly suggests the presence of line nodes and is best modeled by a system consisting of both an s - and a d -wave gap. We also find a potentially magnetic phase which appears below ≈10 K but does not appear to compete with the superconductivity. This compound contains the largest alkali atom in this family of superconductors, and our results yield a value for the in-plane penetration depth of λa b(T =0 ) =244 (3 ) nm .

Cs2UPd3Se6

Directory of Open Access Journals (Sweden)

George N. Oh

2011-02-01

Full Text Available Dicaesium uranium(IV tripalladium(II hexaselenide, Cs2UPd3Se6, crystallizes in the space group Fmmm in the Ba2NaCu3O6 structure type. The asymmetric unit comprises the following atoms with site symmetries as shown: U1 (mm2, Cs1 (222, Cs2 (m2m, Pd1 (.m., Pd2 (2mm, Se1 (m.., and Se2 (1. This layered structure contains six edge-sharing square-planar [PdSe4] units that form a hexagon. These, in turn, edge-share with [USe6] trigonal–prismatic units, forming an extended layer parallel to (010. The layers are stacked along [010]. They are staggered, and are separated by the Cs atoms. The Cs atoms are either coordinated in a square antiprism of Se atoms or are ten-coordinate, with one square face and the opposite face hexagonal.

Cesium platinide hydride 4Cs{sub 2}Pt.CsH: an intermetallic double salt featuring metal anions

Energy Technology Data Exchange (ETDEWEB)

Smetana, Volodymyr [Ames Laboratory, US Department of Energy, and Critical Materials Institute, Ames, Iowa, 50011-3020 (United States); Mudring, Anja-Verena [Ames Laboratory, US Department of Energy, and Critical Materials Institute, Ames, Iowa, 50011-3020 (United States); Department of Materials Sciences and Engineering, Iowa State University, Ames, Iowa, 50011-3111 (United States)

2016-11-14

With Cs{sub 9}Pt{sub 4}H a new representative of ionic compounds featuring metal anions can be added to this rare-membered family. Cs{sub 9}Pt{sub 4}H exhibits a complex crystal structure containing Cs{sup +} cations, Pt{sup 2-} and H{sup -} anions. Being a red, transparent compound its band gap is in the visible range of the electromagnetic spectrum and the ionic type of bonding is confirmed by quantum chemical calculations. This cesium platinide hydride can formally be considered as a double salt of the ''alloy'' cesium-platinum, or better cesium platinide, Cs{sub 2}Pt, and the salt cesium hydride CsH according to Cs{sub 9}Pt{sub 4}H≡4 Cs{sub 2}Pt.CsH. (copyright 2016 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

Techniques on semiautomatic segmentation using the Adobe Photoshop

Science.gov (United States)

Park, Jin Seo; Chung, Min Suk; Hwang, Sung Bae

2005-04-01

The purpose of this research is to enable anybody to semiautomatically segment the anatomical structures in the MRIs, CTs, and other medical images on the personal computer. The segmented images are used for making three-dimensional images, which are helpful in medical education and research. To achieve this purpose, the following trials were performed. The entire body of a volunteer was MR scanned to make 557 MRIs, which were transferred to a personal computer. On Adobe Photoshop, contours of 19 anatomical structures in the MRIs were semiautomatically drawn using MAGNETIC LASSO TOOL; successively, manually corrected using either LASSO TOOL or DIRECT SELECTION TOOL to make 557 segmented images. In a likewise manner, 11 anatomical structures in the 8,500 anatomcial images were segmented. Also, 12 brain and 10 heart anatomical structures in anatomical images were segmented. Proper segmentation was verified by making and examining the coronal, sagittal, and three-dimensional images from the segmented images. During semiautomatic segmentation on Adobe Photoshop, suitable algorithm could be used, the extent of automatization could be regulated, convenient user interface could be used, and software bugs rarely occurred. The techniques of semiautomatic segmentation using Adobe Photoshop are expected to be widely used for segmentation of the anatomical structures in various medical images.

Absorption spectra of CsNd(MoO4)2 and CsGd(MoO4)2-Nd3+ crystals in strong magnetic fields

International Nuclear Information System (INIS)

Gorban', I.S.; Kozeeva, L.P.; Slobodyanyuk, A.V.; Shevchenko, V.A.

1987-01-01

The comparison of the electronic structure of Nd 3+ in CsNd(MoO 4 ) 2 and CsGd(MoO 4 ) 2 - Nd 3+ crystals is made. It is established that in these crystals the activator centers, mainly, of the certain type with the symmetry of the local environment C 2 are formed. The absorption spectra of self-activated CsNd(MoO 4 ) 2 crystal differ from spectra of CsGd(MoO 4 ) 2 - Nd 3+ by the presence of the vibrating structure. The Stark splittings of energy levels of Nd 3+ in the investigated crystalline matrices are more sensitive to the environment effect than the Zeeman ones. The ground state of Nd 3+ ion in CsNd(MoO 4 ) 2 and CsGd(MoO 4 ) 2 molybdates is characterized by the similar values of g-factors

Crystal structure of CsTb(PO3)4 compound

International Nuclear Information System (INIS)

Palkina, K.K.; Maksimova, S.I.; Kuznetsov, V.G.; Chibiskova, N.T.

1978-01-01

The X-ray structural study of compounds of the CsLn(PO 3 ) 4 series has been made. Found is the presence of two structural types for CsPr(PO 3 ) 4 (cubic and monoclinic modifications), one type for CsNd(PO 3 ) 4 (cubic modification) and for CsTb(PO 3 ) 4 (monoclinic modification). For the CsTb(PO 3 ) 4 monocrystal the lattice parameters are determined: a=7.032 +- 0.001; b=8.705 +- 0.001; c=9.051 +- 0.001 A; α=90 deg, β=90 deg, γ=100 deg, Z=2, V=545.68 A 3 , dsub(exp)=3.70 g/cm 3 . The structure character is presented as infinite chains of (PO 4 ) tetrahedrons, stretched along the ''C'' period. Tb and Cs atoms are rounded by 8 atoms of oxygen. Tb polyhedron are irregular octaapexes or strongly deformed tetragonal antiprisms. Tb-Tb shortest distance is 6.59 A

Photovoltaic Performance of Vapor-Assisted Solution-Processed Layer Polymorph of Cs3Sb2I9.

Science.gov (United States)

Singh, Anupriya; Boopathi, Karunakara Moorthy; Mohapatra, Anisha; Chen, Yang Fang; Li, Gang; Chu, Chih Wei

2018-01-24

The presence of toxic lead (Pb) remains a major obstruction to the commercial application of perovskite solar cells. Although antimony (Sb)-based perovskite-like structures A 3 M 2 X 9 can display potentially useful photovoltaic behavior, solution-processed Sb-based perovskite-like structures usually favor the dimer phase, which has poor photovoltaic properties. In this study, we prepared a layered polymorph of Cs 3 Sb 2 I 9 through solution-processing and studied its photovoltaic properties. The exciton binding energy and exciton lifetime of the layer-form Cs 3 Sb 2 I 9 were approximately 100 meV and 6 ns, respectively. The photovoltaic properties of the layered polymorph were superior to those of the dimer polymorph. A solar cell incorporating the layer-form Cs 3 Sb 2 I 9 exhibited an open-circuit voltage of 0.72 V and a power conversion efficiency of 1.5%-the highest reported for an all-inorganic Sb-based perovskite.

Elastic properties of Cs2HgBr4 and Cs2CdBr4 crystals

International Nuclear Information System (INIS)

Kityk, A.V.; Zadorozhna, A.V.; Shchur, Y.I.; Martynyuk-Lototska, Y.I.; Burak, Y.; Vlokh, O.G.

1998-01-01

Using ultrasonic velocity measurements, all components of the elastic constant matrix C ij , elastic compliances matrix S ij , and linear compressibility constants matrix K ij of orthorhombic Cs 2 HgBr 4 and Cs 2 CdBr 4 crystals have been determined over a wide temperature range, including the region of the phase transition from the normal to the incommensurate phase. Results obtained are considered within the framework of the phenomenological theory. Preliminary analysis of the acoustical properties at room temperature clearly indicates that both crystals are relatively important materials for acousto-optical applications. Copyright (1998) CSIRO Australia

Microbial immobilization and recycling of 137Cs in the organic layers of forest ecosystems: Relationship to environmental conditions, humification and invertebrate activity

International Nuclear Information System (INIS)

Brueckmann, Axel; Wolters, Volkmar

1994-01-01

The 137 Cs content of the microbial biomass in the organic layers of 10 German forest sites was quantified with a modified fumigation/extraction method. A K Cs factor was calculated for biomass 137 Cs from the difference between unfumigated and fumigated samples by means of laboratory cultures. The size of the estimated K Cs factors varied between 1.54 and 2.90 (mean, 2.17; S.D., 0.48). The microflora at the different forest sites contained between 1 and 56% of the total amount of 137 Cs found in the organic layers (mean, 13%). Litterbag experiments showed that 137 Cs was actively transported into the L layer by the microflora and that this effect was enhanced by the mesofauna. It is concluded that the immobilization and recycling of 137 Cs by the microflora in the organic layer of forest soils is determined by three major factors: 137 Cs availability, growth conditions of the microflora and biotic interactions

Digital Imaging: An Adobe Photoshop Course

Science.gov (United States)

Cobb, Kristine

2007-01-01

This article introduces digital imaging, an Adobe Photoshop course at Shrewsbury High School in Shrewsbury, Massachusetts. Students are able to earn art credits to graduate by successfully completing the course. Digital imaging must cover art criteria as well as technical skills. The course begins with tutorials created by the instructor and other…

Crystal Growth and Scintillation Properties of Eu2+ doped Cs4CaI6 and Cs4SrI6

Science.gov (United States)

Stand, L.; Zhuravleva, M.; Chakoumakos, B.; Johnson, J.; Loyd, M.; Wu, Y.; Koschan, M.; Melcher, C. L.

2018-03-01

In this work we present the crystal growth and scintillation properties of two new ternarymetal halide scintillators activated with divalent europium, Cs4CaI6 and Cs4SrI6. Single crystals of each compound were grown in evacuated quartz ampoules via the vertical Bridgman technique using a two-zone transparent furnace. Single crystal X-ray diffraction experiments showed that both crystals have a trigonal (R-3c) structure, with a density of 3.99 g/cm3 and 4.03 g/cm3. The radioluminescence and photoluminescence measurements showed typical luminescence properties due to the 5d-4f radiative transitions in Eu2+. At this early stage of development Cs4SrI6:Eu and Cs4CaI6:Eu have shown very promising scintillation properties, with light yields and energy resolutions of 62,300 ph/MeV and 3.3%, and 51,800 photons/MeV and 3.6% at 662 keV, respectively.

New crystals of the CsHSO{sub 4}–CsH{sub 2}PO{sub 4}–H{sub 2}O system

Energy Technology Data Exchange (ETDEWEB)

Makarova, I. P., E-mail: makarova@crys.ras.ru; Grebenev, V. V.; Komornikov, V. A.; Selezneva, E. V. [Russian Academy of Sciences, Shubnikov Institute of Crystallography, Federal Scientific Research Centre “Crystallography and Photonics,” (Russian Federation)

2016-11-15

Cs{sub 6}H(HSO{sub 4}){sub 3}(H{sub 2}PO{sub 4}){sub 4} crystals, grown for the first time based on an analysis of the phase diagram of the CsHSO{sub 4}–CsH{sub 2}PO{sub 4}–H{sub 2}O ternary system, have been investigated by structural analysis using synchrotron radiation. The atomic structure of the crystals is determined and its specific features are analyzed.

The ESA/ESO/NASA Photoshop FITS Liberator 3: Have your say on new features

Science.gov (United States)

Nielsen, L. H.; Christensen, L. L.; Hurt, R. L.; Nielsen, K.; Johansen, T.

2008-06-01

The popular, free ESA/ESO/NASA Photoshop FITS Liberator image processing software (a plugin for Adobe Photoshop) is about to get simpler, faster and more user-friendly! Here we would like to solicit inputs from the community of users.

New silicate-germanate Cs2Pb2[(Si0.6Ge0.4)2O7] from the series A2Pb2[B2O7], A = K, Cs, B = Si, Ge with the umbrella-like [PbO3]4- group

Science.gov (United States)

Belokoneva, Elena L.; Morozov, Ivan A.; Volkov, Anatoly S.; Dimitrova, Olga V.; Stefanovich, Sergey Yu.

2018-04-01

New silicate-germanate Cs2Pb2[(Si0.6Ge0.4)2O7] was synthesized in multi-components hydrothermal solution with 20 w.% concentration of Cs2CO3 mineralizer, pH = 10. Novel mixed compound belongs to the structure type A2Pb2[B2O7] previously indicated for powders with A = K, B=Si or Ge. Singe crystal structure determination of Cs2Pb2[(Si0.6Ge0.4)2O7] revealed the need for the correction of the space group of the earlier suggested structural model from P-3 to P-3m1, as well as for the splitting of the Pb-atom position. Umbrella-like groups [PbO3]4- are located between [(Si,Ge)O4]4- tetrahedra in mica-like honeycomb layers and play the role of tetrahedra with the Pb-lone-pair as the forth apex. Crystal chemical comparison revealed similarities and differences with the classical structure type of α-celsian Ba[Al2Si2O8] with the tetrahedral double layer. Recently investigated nonlinear optical acentric borates Pb2(BO3)(NO3) and Pb2(BO3)Cl are both related to this structural type, possessing umbrella-like groups [PbO3]4- and honeycomb layers [Pb2(BO3)]+ with the BO3-triangles on the tetrahedral positions.

Photoresponse of CsPbBr3 and Cs4PbBr6 Perovskite Single Crystals.

Science.gov (United States)

Cha, Ji-Hyun; Han, Jae Hoon; Yin, Wenping; Park, Cheolwoo; Park, Yongmin; Ahn, Tae Kyu; Cho, Jeong Ho; Jung, Duk-Young

2017-02-02

High-quality and millimeter-sized perovskite single crystals of CsPbBr 3 and Cs 4 PbBr 6 were prepared in organic solvents and studied for correlation between photocurrent generation and photoluminescence (PL) emission. The CsPbBr 3 crystals, which have a 3D perovskite structure, showed a highly sensitive photoresponse and poor PL signal. In contrast, Cs 4 PbBr 6 crystals, which have a 0D perovskite structure, exhibited more than 1 order of magnitude higher PL intensity than CsPbBr 3 , which generated an ultralow photoresponse under illumination. Their contrasting optoelectrical characteristics were attributed to different exciton binding energies, induced by coordination geometry of the [PbBr 6 ] 4- octahedron sublattices. This work correlated the local structures of lead in the primitive perovskite and its derivatives to PL spectra as well as photoconductivity.

Hepatic volumetry with PhotoShop in personal computer.

Science.gov (United States)

Lu, Yi; Wu, Zheng; Liu, Chang; Wang, Hao-Hua

2004-02-01

Convenient way to clarify liver volume or tumor volume in the liver is eagerly demanded by hepatobiliary surgeons, for so many aspects of clinical work need to know the liver volumetry. At present, some methods have been used to measure the liver volumetry, such as computed tomography (CT) scans, three-dimensional ultrasound volumetric system([1]) and 3-dimensional sonography([2,3]) et al. But enough volumetric information was failed to obtain by surgeons and a new way of measuring the liver volumetry that can be operated by themselves is exigent. Whereas we devise a new method of using PhotoShop in personal computer to measure the liver volumetry. A piece of whole CT film was transformed to a high quality digitized image by digital camera or scanner and then the digitized image was conducted as JPEG file into personal computer. The JPEG image file of CT film was opened by PhotoShop. Determining the edge of interested areas, and the data of pixel values of the interested areas divided by 1 cm2 pixel value will produce the actual area with the unit of square centimeter. If section thickness of CT scan is 1 cm, the sum of the areas of the liver or tumor in all sections naturally is the volume of the liver or tumor. Comparison of 10 hepatic volumes gained by this method and those gained by the GE Prospeed CT set showed a good relativity between the two groups. The volumes of three right lobes were calculated by this method before lobectomy and their real volumes were obtained postoperatively by a volumenometer. Their variation was limited to 5%. Hepatic volume obtained by PhotoShop is reliable. This method can be used to measure hepatic volume perfectly to meet clinical demand, and many parameters such as liver resection rate, graft volume can be achieved. The disadvantage of this method is the step of copying the pixel value from PhotoShop to Microsoft Excel.

Light-emitting diodes based on two-dimensional PA2(CsPbBr3)n-1PbBr4 layered perovskites%基于PA2(CsPbBr3)n-1PbBr4二维层状钙钛矿的电致发光二极管

Institute of Scientific and Technical Information of China (English)

孟妍; 牛连斌; 许龙; 林春燕; 熊自阳; 熊祖洪; 陈平

2018-01-01

remains a major concern.To circumvent this problem,all-inorganic halide perovskites exhibiting higher thermal and chemical stability,such as cesium lead bromide (CsPbBr3),have been used as alternative emitters in PeLED.Despite the advantages described above,both the brightness and the EQE of CsPbBr3-based PeLED remain limited.One important reason for low efficiency of CsPbBr3-based PeLED is the facile dissociation of excitons in 3D perovskites due to their small exciton binding energy.One promising way to enhance the exciton binding energy is reducing the grain size of perovskites.Herein,we report a solution process to form highly uniform and ultra-fiat perovskite films with nanometre-sized grains that allow us to demonstrate efficient PeLED.By mixing long-chain ammonium halides of CH3CH2CH2NH3Br (PABr) with the 3D CsPbBr3 perovskite precursor solution,the growth of 3D perovskite grains are dramatically impeded and the PA2(CsPbBr3)n-1PbBr4 quantum dots with grain size of ～100 nm were achieved.This is because the long-chain ammonium ions cannot fill the comer of PbBr4 octahedral layers and therefore impedes the 3D perovskite formation.Moreover,the nanometre-sized grains feature reduced dimensionality,starting a transition from 3D to 2D layered (so-called Ruddlesden-Popper phase) perovskite structures.The SEM image show the morphology of PA2(CsPbBr3)n-1PbBr4 layer was dense and uniform,which is very important to suppress the leaking current in the PeLED.We found that PA2(CsPbBr3)n-1PbBr4 film mainly consists of two different 2D structures,namely PA2PbBr4 (n=l) and PA2(CsPbBr3)PbBr4 (n=2),according to the analysis of XRD pattern.Compared to the single UVs absorption peak of CsPbBr3 at ～520 nm,PA2(CsPbBr3)n-1PbBr4 film show multiple absorption peaks,indicating several extonic states are formed upon light excitation.Although several extonic states exist,photoluminescence (PL) with only one peak of 506 nm was observed in PA2(CsPbBr3)n-1PbBr4 film.We suspect that the energy

Creating animated GIF files for electronic presentations using Photoshop.

Science.gov (United States)

Yam, Chun-Shan; Kruskal, Jonathan; Larson, Michael

2007-05-01

Our objective is to present a simple method for converting movie clips to animated GIFs (graphics interchange format) using Photoshop. Although animated GIF is a more reliable format than movie clips (e.g., AVI and QuickTime) for presenting dynamic data sets in PowerPoint presentations, this output format is not available on most radiology workstations. Therefore, many academic radiologists still experience the problem of incompatible codecs and missing file links when trying to show movie clips in their PowerPoint presentations. One way to resolve this issue is to convert the movie clips to animated GIFs. In this article, we provide a simple method for this conversion using Photoshop--a common software application used by radiologists.

[Use of Adobe Photoshop software in medical criminology].

Science.gov (United States)

Nikitin, S A; Demidov, I V

2000-01-01

Describes the method of comparative analysis of various objects in practical medical criminology and making of high-quality photographs with the use of Adobe Photoshop software. Options of the software needed for expert evaluations are enumerated.

Image editing with Adobe Photoshop 6.0.

Science.gov (United States)

Caruso, Ronald D; Postel, Gregory C

2002-01-01

The authors introduce Photoshop 6.0 for radiologists and demonstrate basic techniques of editing gray-scale cross-sectional images intended for publication and for incorporation into computerized presentations. For basic editing of gray-scale cross-sectional images, the Tools palette and the History/Actions palette pair should be displayed. The History palette may be used to undo a step or series of steps. The Actions palette is a menu of user-defined macros that save time by automating an action or series of actions. Converting an image to 8-bit gray scale is the first editing function. Cropping is the next action. Both decrease file size. Use of the smallest file size necessary for the purpose at hand is recommended. Final file size for gray-scale cross-sectional neuroradiologic images (8-bit, single-layer TIFF [tagged image file format] at 300 pixels per inch) intended for publication varies from about 700 Kbytes to 3 Mbytes. Final file size for incorporation into computerized presentations is about 10-100 Kbytes (8-bit, single-layer, gray-scale, high-quality JPEG [Joint Photographic Experts Group]), depending on source and intended use. Editing and annotating images before they are inserted into presentation software is highly recommended, both for convenience and flexibility. Radiologists should find that image editing can be carried out very rapidly once the basic steps are learned and automated. Copyright RSNA, 2002

Adobe Photoshop images software in the verification of radiation portal

International Nuclear Information System (INIS)

Ouyang Shuigen; Wang Xiaohu; Liu Zhiqiang; Wei Xiyi; Qi Yong

2010-01-01

Objective: To investigate the value of Adobe Photoshop images software in the verification of radiation portal. Methods: The portal and simulation films or CT reconstruction images were imported into computer using a scanner. The image size, gray scale and contrast scale were adjusted with Adobe Photoshop images software, then image registration and measurement were completed. Results: By the comparison between portal image and simulation image, the set-up errors in right-left, superior-inferior and anterior-posterior directions were (1.11 ± 1.37) mm, (1.33 ± 1.25) mm and (0.83±0.79) mm in the head and neck;(1.44±1.03) mm,(1.6±1.52) mm and (1.34±1.17) mm in the thorax;(1.53±0.86) mm, (1.83 ± 1.19) mm and (1.67 ± 0.68)mm in the abdomen; (1.93 ± I. 83) mm, (1.59 ± 1.07)mm and (0.85 ± 0.72)mm in the pelvic cavity. Conclusions: Accurate radiation portal verification and position measurement can be completed by using Adobe Photoshop, which is a simple, safe and reliable method. (authors)

Photoshop Elements 6 The Missing Manual

CERN Document Server

Brundage, Barbara

2009-01-01

With Photoshop Elements 6, the most popular photo-editing program on Earth just keeps getting better. It's perfect for scrapbooking, email-ready slideshows, Web galleries, you name it. But knowing what to do and when is tricky. That's why our Missing Manual is the bestselling book on the topic. This fully revised guide explains not only how the tools and commands work, but when to use them.

Complete chromogen separation and analysis in double immunohistochemical stains using Photoshop-based image analysis.

Science.gov (United States)

Lehr, H A; van der Loos, C M; Teeling, P; Gown, A M

1999-01-01

Simultaneous detection of two different antigens on paraffin-embedded and frozen tissues can be accomplished by double immunohistochemistry. However, many double chromogen systems suffer from signal overlap, precluding definite signal quantification. To separate and quantitatively analyze the different chromogens, we imported images into a Macintosh computer using a CCD camera attached to a diagnostic microscope and used Photoshop software for the recognition, selection, and separation of colors. We show here that Photoshop-based image analysis allows complete separation of chromogens not only on the basis of their RGB spectral characteristics, but also on the basis of information concerning saturation, hue, and luminosity intrinsic to the digitized images. We demonstrate that Photoshop-based image analysis provides superior results compared to color separation using bandpass filters. Quantification of the individual chromogens is then provided by Photoshop using the Histogram command, which supplies information on the luminosity (corresponding to gray levels of black-and-white images) and on the number of pixels as a measure of spatial distribution. (J Histochem Cytochem 47:119-125, 1999)

Preprocessing with Photoshop Software on Microscopic Images of A549 Cells in Epithelial-Mesenchymal Transition.

Science.gov (United States)

Ren, Zhou-Xin; Yu, Hai-Bin; Shen, Jun-Ling; Li, Ya; Li, Jian-Sheng

2015-06-01

To establish a preprocessing method for cell morphometry in microscopic images of A549 cells in epithelial-mesenchymal transition (EMT). Adobe Photoshop CS2 (Adobe Systems, Inc.) was used for preprocessing the images. First, all images were processed for size uniformity and high distinguishability between the cell and background area. Then, a blank image with the same size and grids was established and cross points of the grids were added into a distinct color. The blank image was merged into a processed image. In the merged images, the cells with 1 or more cross points were chosen, and then the cell areas were enclosed and were replaced in a distinct color. Except for chosen cellular areas, all areas were changed into a unique hue. Three observers quantified roundness of cells in images with the image preprocess (IPP) or without the method (Controls), respectively. Furthermore, 1 observer measured the roundness 3 times with the 2 methods, respectively. The results between IPPs and Controls were compared for repeatability and reproducibility. As compared with the Control method, among 3 observers, use of the IPP method resulted in a higher number and a higher percentage of same-chosen cells in an image. The relative average deviation values of roundness, either for 3 observers or 1 observer, were significantly higher in Controls than in IPPs (p Photoshop, a chosen cell from an image was more objective, regular, and accurate, creating an increase of reproducibility and repeatability on morphometry of A549 cells in epithelial to mesenchymal transition.

Simplified Perovskite Solar Cell with 4.1% Efficiency Employing Inorganic CsPbBr3 as Light Absorber.

Science.gov (United States)

Duan, Jialong; Zhao, Yuanyuan; He, Benlin; Tang, Qunwei

2018-04-17

Perovskite solar cells with cost-effectiveness, high power conversion efficiency, and improved stability are promising solutions to the energy crisis and environmental pollution. However, a wide-bandgap inorganic-semiconductor electron-transporting layer such as TiO 2 can harvest ultraviolet light to photodegrade perovskite halides, and the high cost of a state-of-the-art hole-transporting layer is an economic burden for commercialization. Here, the building of a simplified cesium lead bromide (CsPbBr 3 ) perovskite solar cell with fluorine-doped tin oxide (FTO)/CsPbBr 3 /carbon architecture by a multistep solution-processed deposition technology is demonstrated, achieving an efficiency as high as 4.1% and improved stability upon interfacial modification by graphene quantum dots and CsPbBrI 2 quantum dots. This work provides new opportunities of building next-generation solar cells with significantly simplified processes and reduced production costs. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Structural diversities induced by cation sizes in a series of fluorogermanophosphates: A2[GeF2(HPO4)2] (A = Na, K, Rb, NH4, and Cs).

Science.gov (United States)

Chen, Zhang-Gai; Huang, Xia; Zhuang, Rong-Chuan; Zhang, Yu; Liu, Xin; Shi, Tao; Wang, Shuai-Hua; Wu, Shao-Fan; Mi, Jin-Xiao; Huang, Ya-Xi

2017-09-12

Germanophosphates, in comparison with other metal phosphates, have been less studied but potentially exhibit more diverse structural chemistry with wide applications. Herein we applied a hydro-/solvo-fluorothermal route to make use of both the "tailor effect" of fluoride for the formation of low dimensional anionic clusters and the presence of alkali cations of different sizes to align the anionic clusters to control the overall crystal symmetries of germanophosphates. The synergetic effects of fluoride and alkali cations led to structural changes from chain-like structures to layered structures in a series of five novel fluorogermanophosphates: A 2 [GeF 2 (HPO 4 ) 2 ] (A = Na, K, Rb, NH 4 , and Cs, denoted as Na, K, Rb, NH4, and Cs). Although these fluorogermanophosphates have stoichiometrically equivalent formulas, they feature different anionic clusters, diverse structural dimensionalities, and contrasting crystal symmetries. Chain-like structures were observed for the compounds with the smaller sized alkali ions (Na + , K + , and Rb + ), whereas layered structures were found for those containing the larger sized cations ((NH 4 ) + and Cs + ). Specifically, monoclinic space groups were observed for the Na, K, Rb, and NH4 compounds, whereas a tetragonal space group P4/mbm was found for the Cs compound. These compounds provide new insights into the effects of cation sizes on the anionic clusters built from GeO 4 F 2 octahedra and HPO 4 tetrahedra as well as their influences on the overall structural symmetries in germanophosphates. Further characterization including IR spectroscopy and thermal analyses for all five compounds is also presented.

Variable dimensionality and framework found in a series of quaternary zinc selenites, A2Zn3(SeO3)4·xH2O (A = Na, Rb, and Cs; 0≤x≤1) and Cs2Zn2(SeO3)3·2H2O

Science.gov (United States)

Lü, Minfeng; Jo, Hongil; Oh, Seung-Jin; Ok, Kang Min

2017-01-01

Five new alkali metal zinc selenites, A2Zn3(SeO3)4·xH2O (A = Na, Rb, and Cs; 0≤x≤1) and Cs2Zn2(SeO3)3·2H2O have been synthesized by heating a mixture of ZnO, SeO2 and A2CO3 (A = Na, Rb, and Cs), and characterized by X-ray diffraction (XRD) and spectroscopic analyses techniques. All of the reported materials revealed a rich structural chemistry with different frameworks and connection modes of Zn2+. While Rb2Zn3(SeO3)4 and Cs2Zn3(SeO3)4·H2O revealed three-dimensional frameworks consisting of isolated ZnO4 tetrahedra and SeO3 polyhedra, Na2Zn3(SeO3)4, Cs2Zn3(SeO3)4, and Cs2Zn2(SeO3)3·2H2O contained two-dimensional [Zn3(SeO3)4]2- layers. Specifically, whereas isolated ZnO4 tetrahedra and SeO3 polyhedra are arranged into two-dimensional [Zn3(SeO3)4]2- layers in two cesium compounds, circular [Zn3O10]14- chains and SeO3 linkers are formed in two-dimensional [Zn3(SeO3)4]2- layers in Na2Zn3(SeO3)4. Close structural examinations suggest that the size of alkali metal is significant in determining the framework geometry as well as connection modes of transition metal cations.

Efficient small molecular organic light emitting diode with graphene cathode covered by a Sm layer with nano-hollows and n-doped by Bphen:Cs2CO3 in the hollows

Science.gov (United States)

Yao, Li; Li, Lei; Qin, Laixiang; Ma, Yaoguang; Wang, Wei; Meng, Hu; Jin, Weifeng; Wang, Yilun; Xu, Wanjin; Ran, Guangzhao; You, Liping; Qin, Guogang

2017-03-01

Graphene is a favorable candidate for electrodes of organic light emitting diodes (OLEDs). Graphene has quite a high work function of ˜4.5 eV, and has been extensively studied when used as anodes of OLEDs. In order to use graphene as a cathode, the electron injection barrier between the graphene cathode and the electron transport layer has to be low enough. Using 4,7-diphenyl-1,10-phenanthroline (Bphen):Cs2CO3 to n-dope graphene is a very good method, but the electron injection barrier between the n-doped graphene and Bphen:Cs2CO3 is still too high to be ˜1.0 eV. In this work, in order to further reduce the electron injection barrier, a novel method is suggested. On the graphene cathode, a Sm layer with a lot of nano-hollows, and subsequently a layer of Bphen:Cs2CO3, are deposited. The Bphen:Cs2CO3 can n-dope graphene in the nano-hollows, and the Fermi level of the graphene rises. The nano Sm layer is very easily oxidized. Oxygen adsorbed on the surface of graphene may react with Sm to form an O--Sm+ dipole layer. On the areas of the Sm oxide dipole layer without nano-hollows, the electron injection barrier can be further lowered by the dipole layer. Electrons tend to mainly inject through the lower electron barrier where the dipole layer exists. Based on this idea, an effective inverted small molecular OLED with the structure of graphene/1 nm Sm layer with a lot of nano-hollows/Bphen:Cs2CO3/Alq3:C545T/NPB/MoO3/Al is presented. The maximum current efficiency and maximum power efficiency of the OLED with a 1 nm Sm layer are about two and three times of those of the reference OLED without any Sm layer, respectively.

Influence of the number of layers on ultrathin CsSnI3 perovskite: from electronic structure to carrier mobility

Science.gov (United States)

Liu, Biao; Long, Mengqiu; Cai, Meng-Qiu; Yang, Junliang

2018-03-01

Inorganic halide perovskites have attracted great attention in recent years as promising materials for optoelectronic devices, with ultrathin inorganic halide perovskites showing excellent properties and great potential applications. Herein, the intrinsic electronic and optical properties of ultrathin cesium tin tri-iodide (CsSnI3) perovskite with a varying number of layers are explored using first-principles calculations. The results reveal that ultrathin CsSnI3 is a direct band gap semiconductor, and the band gap continues to increase to 1.83 eV from 1.28 eV as the number of layers is reduced to one layer from the bulk. By decreasing the number of layers, the effective mass of ultrathin CsSnI3 increases, and the optical absorption intensity along the x and y directions shows that the linear dichroism becomes stronger and stronger. Furthermore, the carrier mobilities (µ) can be predicted, and they show obvious in-plane anisotropy. The µ of the electrons is higher than that of the holes, and the electron mobility along the y direction is higher than that along the x direction. The layer thickness does not distinctly influence the µ. The difference in the atomic orbital distribution has the nature of obvious anisotropy in ultrathin CsSnI3. This work suggests that ultrathin inorganic perovskite could be a potential candidate for future nano-optoelectronic devices.

[Landmark-based automatic registration of serial cross-sectional images of Chinese digital human using Photoshop and Matlab software].

Science.gov (United States)

Su, Xiu-yun; Pei, Guo-xian; Yu, Bin; Hu, Yan-ling; Li, Jin; Huang, Qian; Li, Xu; Zhang, Yuan-zhi

2007-12-01

This paper describes automatic registration of the serial cross-sectional images of Chinese digital human by projective registration method based on the landmarks using the commercially available software Photoshop and Matlab. During cadaver embedment for acquisition of the Chinese digital human images, 4 rods were placed parallel to the vertical axis of the frozen cadaver to allow orientation. Projective distortion of the rod positions on the cross-sectional images was inevitable due to even slight changes of the relative position of the camera. The original cross-sectional images were first processed using Photoshop software firstly to obtain the images of the orientation rods, and the centroid coordinate of every rod image was acquired with Matlab software. With the average coordinate value of the rods as the fiducial point, two-dimensional projective transformation coefficient of each image was determined. Projective transformation was then carried out and projective distortion from each original serial image was eliminated. The rectified cross-sectional images were again processed using Photoshop to obtain the image of the first orientation rod, the coordinate value of first rod image was calculated using Matlab software, and the cross-sectional images were cut into images of the same size according to the first rod spatial coordinate, to achieve automatic registration of the serial cross-sectional images. sing Photoshop and Matlab softwares, projective transformation can accurately accomplish the image registration for the serial images with simpler calculation processes and easier computer processing.

Thermal, conductivity, NMR, and Raman spectroscopic measurements and phase diagram of the Cs2S2O7-CsHSO4 system

DEFF Research Database (Denmark)

Rasmussen, Søren Birk; Hama, Hind; Lapina, Olga

2003-01-01

The conductivity of the binary system CS2S2O7-CsHSO4 has been measured at 20 different molten compositions in the full composition range and in the temperature range 430-750 K. From the obtained liquidus-solidus phase transition temperatures, the phase diagram has been constructed. It is of the s......The conductivity of the binary system CS2S2O7-CsHSO4 has been measured at 20 different molten compositions in the full composition range and in the temperature range 430-750 K. From the obtained liquidus-solidus phase transition temperatures, the phase diagram has been constructed...... from the NMR measurements on CsHSO4, CS2S2O7, and Cs2S2O7-CsHSO4 mixtures. For 11 selected compositions covering the entire composition range of the CS2S2O7-CsHSO4 binary system, the conductivity of the molten state has been expressed by equations of the form k(X) = A(X) + B(X)(T - T-m) + C(X)(T - T...

Postsynthesis Transformation of Insulating Cs4PbBr6 Nanocrystals into Bright Perovskite CsPbBr3 through Physical and Chemical Extraction of CsBr.

Science.gov (United States)

Palazon, Francisco; Urso, Carmine; De Trizio, Luca; Akkerman, Quinten; Marras, Sergio; Locardi, Federico; Nelli, Ilaria; Ferretti, Maurizio; Prato, Mirko; Manna, Liberato

2017-10-13

Perovskite-related Cs 4 PbBr 6 nanocrystals present a "zero-dimensional" crystalline structure where adjacent [PbBr 6 ] 4- octahedra do not share any corners. We show in this work that these nanocrystals can be converted into "three-dimensional" CsPbBr 3 perovskites by extraction of CsBr. This conversion drastically changes the optoelectronic properties of the nanocrystals that become highly photoluminescent. The extraction of CsBr can be achieved either by thermal annealing (physical approach) or by chemical reaction with Prussian Blue (chemical approach). The former approach can be simply carried out on a dried film without addition of any chemicals but does not yield a full transformation. Instead, reaction with Prussian Blue in solution achieves a full transformation into the perovskite phase. This transformation was also verified on the iodide counterpart (Cs 4 PbI 6 ).

Molecular studies of Cs adsorption sites in inorganic layered materials: the influence of solution concentration.

Science.gov (United States)

Sato, Kiminori; Hunger, Michael

2017-07-19

Radioactive Cs released into a soil environment migrates along with groundwater in a manner dependent on Cs concentration. Data on the variation of Cs adsorption as a function of solution concentration are an essential prerequisite to successful decontamination work in Fukushima. To aid the ongoing decontamination work, the adsorption of Cs in aqueous solution across a wide Cs + molarity range is studied for the case of saponite clay as adsorbent, an inorganic layered material that is an abundant mineral in the soil environment. The local molecular structures, i.e. nanosheet surfaces, nanosheet edges, and oncoming hexagonal cavities, participating in Cs adsorption are qualitatively highlighted by means of a recently developed analytical method using data from a conventional elution test, 133 Cs magic-angle-spinning nuclear magnetic resonance (MAS NMR), and the radiocesium interception potential (RIP) [K. Sato, et al., J. Phys. Chem. C, 2016, 120, 1270]. The concentrations of nanosheet edges amount to between 100 and 400 mmol kg -1 , which are not substantially different from those of the nanosheet surfaces, generally regarded as the main decontamination sites. This unambiguously implies that the nanosheet edges should be targeted as the molecular sites for decontaminating radioactive Cs, in addition to the nanosheet surfaces.

Technical report on semiautomatic segmentation using the Adobe Photoshop.

Science.gov (United States)

Park, Jin Seo; Chung, Min Suk; Hwang, Sung Bae; Lee, Yong Sook; Har, Dong-Hwan

2005-12-01

The purpose of this research is to enable users to semiautomatically segment the anatomical structures in magnetic resonance images (MRIs), computerized tomographs (CTs), and other medical images on a personal computer. The segmented images are used for making 3D images, which are helpful to medical education and research. To achieve this purpose, the following trials were performed. The entire body of a volunteer was scanned to make 557 MRIs. On Adobe Photoshop, contours of 19 anatomical structures in the MRIs were semiautomatically drawn using MAGNETIC LASSO TOOL and manually corrected using either LASSO TOOL or DIRECT SELECTION TOOL to make 557 segmented images. In a similar manner, 13 anatomical structures in 8,590 anatomical images were segmented. Proper segmentation was verified by making 3D images from the segmented images. Semiautomatic segmentation using Adobe Photoshop is expected to be widely used for segmentation of anatomical structures in various medical images.

Hybridization of Single Nanocrystals of Cs4PbBr6 and CsPbBr3

OpenAIRE

Weerd, Chris de; Lin, Junhao; Gomez, Leyre; Fujiwara, Yasufumi; Suenaga, Kazutomo; Gregorkiewicz, Tom

2017-01-01

Nanocrystals of all-inorganic cesium lead halide perovskites (CsPbX3, X = Cl, Br, I) feature high absorption and efficient narrow-band emission which renders them promising for future generation of photovoltaic and optoelectronic devices. Colloidal ensembles of these nanocrystals can be conveniently prepared by chemical synthesis. However, in the case of CsPbBr3, its synthesis can also yield nanocrystals of Cs4PbBr6 and the properties of the two are easily confused. Here, we investigate in de...

Acid-base chemistry and proton conductivity of CsHSO₄, CsH₂PO₄ and their mixtures with N-heterocycles  

DEFF Research Database (Denmark)

Aili, David; Gao, Ying; Han, Junyoung

2017-01-01

temperature range of CsH2PO4 as well. Binary mixtures of CsH2PO4 with 1,2,4-triazole, benzimidazole or imidazole were prepared by means of mechanochemical synthesis. Mixtures based on CsHSO4 were prepared as a basis for a comparative discussion. It was found that CsHSO4 formed organic-inorganic salts, while...

An easy and inexpensive method for quantitative analysis of endothelial damage by using vital dye staining and Adobe Photoshop software.

Science.gov (United States)

Saad, Hisham A; Terry, Mark A; Shamie, Neda; Chen, Edwin S; Friend, Daniel F; Holiman, Jeffrey D; Stoeger, Christopher

2008-08-01

We developed a simple, practical, and inexpensive technique to analyze areas of endothelial cell loss and/or damage over the entire corneal area after vital dye staining by using a readily available, off-the-shelf, consumer software program, Adobe Photoshop. The purpose of this article is to convey a method of quantifying areas of cell loss and/or damage. Descemet-stripping automated endothelial keratoplasty corneal transplant surgery was performed by using 5 precut corneas on a human cadaver eye. Corneas were removed and stained with trypan blue and alizarin red S and subsequently photographed. Quantitative assessment of endothelial damage was performed by using Adobe Photoshop 7.0 software. The average difference for cell area damage for analyses performed by 1 observer twice was 1.41%. For analyses performed by 2 observers, the average difference was 1.71%. Three masked observers were 100% successful in matching the randomized stained corneas to their randomized processed Adobe images. Vital dye staining of corneal endothelial cells can be combined with Adobe Photoshop software to yield a quantitative assessment of areas of acute endothelial cell loss and/or damage. This described technique holds promise for a more consistent and accurate method to evaluate the surgical trauma to the endothelial cell layer in laboratory models. This method of quantitative analysis can probably be generalized to any area of research that involves areas that are differentiated by color or contrast.

Vibrational spectra of Cs2Cu(SO4)2·6H2O and Cs2Cu(SeO4)2·nH2O (n = 4, 6) with a crystal structure determination of the Tutton salt Cs2Cu(SeO4)2·6H2O

Science.gov (United States)

Wildner, M.; Marinova, D.; Stoilova, D.

2016-02-01

The solubility in the three-component systems Cs2SO4-CuSO4-H2O and Cs2SeO4-CuSeO4-H2O have been studied at 25 °C. The experimental results show that double salts, Cs2Cu(SO4)2·6H2O and Cs2Cu(SeO4)2·4H2O, crystallize from the ternary solutions within large concentration ranges. Crystals of Cs2Cu(SeO4)2·6H2O were synthesized at somewhat lower temperatures (7-8 °C). The thermal dehydration of the title compounds was studied by TG, DTA and DSC methods and the respective dehydration schemes are proposed. The calculated enthalpies of dehydration (ΔHdeh) have values of: 434.2 kJ mol-1 (Cs2Cu(SeO4)2·6H2O), 280.9 kJ mol-1 (Cs2Cu(SeO4)2·4H2O), and 420.2 kJ mol-1 (the phase transition of Cs2Cu(SO4)2·6H2O into Cs2Cu(SO4)2·H2O). The crystal structure of Cs2Cu(SeO4)2ṡ6H2O was determined from single crystal X-ray diffraction data. It belongs to the group of Tutton salts, crystallizing isotypic to the respective sulfate in a monoclinic structure which is characterized by isolated Cu(H2O)6 octahedra and SeO4 tetrahedra, interlinked by hydrogen bonds and [9]-coordinated Cs+ cations. Infrared spectra of the cesium copper compounds are presented and discussed with respect to both the normal modes of the tetrahedral ions and the water molecules. The analysis of the infrared spectra of the double compounds reveals that the distortion of the selenate tetrahedra in Cs2Cu(SeO4)2·4H2O is stronger than those in Cs2Cu(SeO4)2·6H2O in agreement with the structural data. Matrix-infrared spectroscopy was applied to confirm this claim - Δν3 for SO4 2 - ions matrix-isolated in Cs2Cu(SeO4)2·6H2O has a value of 35 cm-1 and that of the same ions included in Cs2Cu(SeO4)2·4H2O - 84 cm-1. This spectroscopic finding is due to the formation of strong covalent bands Cu-OSO3 on one hand, and on the other to the stronger deformation of the host SeO4 2 - tetrahedra in Cs2Cu(SeO4)2·4H2O as compared to those in Cs2Cu(SeO4)2·6H2O. The strength of the hydrogen bonds as deduced from the

Variable dimensionality and framework found in a series of quaternary zinc selenites, A2Zn3(SeO3)4·xH2O (A = Na, Rb, and Cs; 0≤x≤1) and Cs2Zn2(SeO3)3·2H2O

International Nuclear Information System (INIS)

Lü, Minfeng; Jo, Hongil; Oh, Seung-Jin; Ok, Kang Min

2017-01-01

Five new alkali metal zinc selenites, A 2 Zn 3 (SeO 3 ) 4 ·xH 2 O (A = Na, Rb, and Cs; 0≤x≤1) and Cs 2 Zn 2 (SeO 3 ) 3 ·2H 2 O have been synthesized by heating a mixture of ZnO, SeO 2 and A 2 CO 3 (A = Na, Rb, and Cs), and characterized by X-ray diffraction (XRD) and spectroscopic analyses techniques. All of the reported materials revealed a rich structural chemistry with different frameworks and connection modes of Zn 2+ . While Rb 2 Zn 3 (SeO 3 ) 4 and Cs 2 Zn 3 (SeO 3 ) 4 ·H 2 O revealed three-dimensional frameworks consisting of isolated ZnO 4 tetrahedra and SeO 3 polyhedra, Na 2 Zn 3 (SeO 3 ) 4 , Cs 2 Zn 3 (SeO 3 ) 4 , and Cs 2 Zn 2 (SeO 3 ) 3 ·2H 2 O contained two-dimensional [Zn 3 (SeO 3 ) 4 ] 2- layers. Specifically, whereas isolated ZnO 4 tetrahedra and SeO 3 polyhedra are arranged into two-dimensional [Zn 3 (SeO 3 ) 4 ] 2- layers in two cesium compounds, circular [Zn 3 O 10 ] 14- chains and SeO 3 linkers are formed in two-dimensional [Zn 3 (SeO 3 ) 4 ] 2- layers in Na 2 Zn 3 (SeO 3 ) 4 . Close structural examinations suggest that the size of alkali metal is significant in determining the framework geometry as well as connection modes of transition metal cations. - Graphical abstract: Variable dimensions and frameworks were found in a series of quaternary zinc selenites, A 2 Zn 3 (SeO 3 ) 4 (A = Na, Rb and Cs). - Highlights: • Five novel quaternary zinc selenites are synthesized. • All the selenites with different structures contain polarizable d 10 and lone pair cations. • The size of alkali metal cations is significant in determining the framework geometry.

The two-dimensional thiophosphate CsCrP2S7

Directory of Open Access Journals (Sweden)

Kyounghee Kim

2010-09-01

Full Text Available The quaternary title compound, caesium chromium(III heptathiodiphosphate(V, CsCrP2S7, has been synthesized using the reactive halide flux method. It is isotypic with other AMP2S7 (A = alkali metal; M = Cr, V or In structures and consists of two-dimensional ∞2[CrP2S7]− layers extending parallel to (001 which are separated from each other by Cs+ ions (symmetry 2. The layer is built up from slightly distorted octahedral [CrS6] units (symmetry 2 and bent [P2S7] units consisting of two corner-sharing [PS4] tetrahedra. The [CrS6] octahedra share two edges and two corners with the [PS4] tetrahedra. There are only van der Waals interactions present between the layers. The Cs+ ions are located in this van der Waals gap and stabilize the structure through weak ionic interactions. The classical charge balance of the title compound can be expressed as [Cs+][Cr3+][P5+]2[S2−]7.

Pure Cs4PbBr6: Highly Luminescent Zero-Dimensional Perovskite Solids

KAUST Repository

Saidaminov, Makhsud I.

2016-09-26

So-called zero-dimensional perovskites, such as Cs4PbBr6, promise outstanding emissive properties. However, Cs4PbBr6 is mostly prepared by melting of precursors that usually leads to a coformation of undesired phases. Here, we report a simple low-temperature solution-processed synthesis of pure Cs4PbBr6 with remarkable emission properties. We found that pure Cs4PbBr6 in solid form exhibits a 45% photoluminescence quantum yield (PLQY), in contrast to its three-dimensional counterpart, CsPbBr3, which exhibits more than 2 orders of magnitude lower PLQY. Such a PLQY of Cs4PbBr6 is significantly higher than that of other solid forms of lower-dimensional metal halide perovskite derivatives and perovskite nanocrystals. We attribute this dramatic increase in PL to the high exciton binding energy, which we estimate to be ∼353 meV, likely induced by the unique Bergerhoff–Schmitz–Dumont-type crystal structure of Cs4PbBr6, in which metal-halide-comprised octahedra are spatially confined. Our findings bring this class of perovskite derivatives to the forefront of color-converting and light-emitting applications.

Single-crystal X-ray diffraction study of Cs2Er[Si6O14]F and Cs2Er[Si4O10]F

International Nuclear Information System (INIS)

Dabic, Predrag; Kremenovic, Aleksandar; Vulic, Predag; Kahlenberg, Volker; Schmidmair, Daniela

2016-01-01

Single-crystal growth experiments in the system CsF-Er 2 O 3 -SiO 2 resulted in the simultaneous crystallization of two chemically related compounds within the same run: Cs 2 Er[Si 6 O 14 ]F (phase I) and Cs 2 Er[Si 4 O 10 ]F (phase II). They represent the first examples for cesium erbium silicates containing fluorine. Basic crystallographic data are - phase I: space group Cmca, a=17.2556(6) Aa, b=24.6565(7) Aa, c=14.4735(5) Aa, V=6157.9(3) Aa 3 , Z=16; phase II: space group Pnma, a=22.3748(7) Aa, b=8.8390(2) Aa, c=11.9710(4) Aa, V=2367.5(1) Aa 3 , Z=8. The structures were determined by direct methods and refined to residuals of R(vertical stroke F vertical stroke)=0.0229 for 2920 (phase I) and 0.0231 for 2314 (phase II) independent observed reflections with I>2σ(I). The structure of phase I represents a previously unknown structure type with a three dimensional tetrahedral framework consisting of Q 3 and Q 4 groups in the ratio 2:1. Basic building units of the network are unbranched sechser single-chains running parallel to [001]. The network can be conveniently built up from the condensation of tetrahedral layers parallel to (010) or (100), respectively. The crystal structure of phase II can be classified as a tubular or columnar chain silicate indicating that the backbones of the structure are multiple chains of silicate tetrahedra. This structure is isotypic to a Cs 2 Y[Si 4 O 10 ]F, a compound that has been characterized previously. Alternatively, both compounds can be described as mixed octahedral-tetrahedral frameworks, which can be classified according to their polyhedral microensembles. A topological analysis of both nets is presented.

Enthalpy-increment measurements for CsI(s) and Cs2CrO4(s) by high-temperature Calvet calorimetry

International Nuclear Information System (INIS)

Venugopal, V.; Agarwal, R.; Roy, K.N.; Prasad, R.; Sood, D.D.

1987-01-01

Molar thermodynamic properties of CsI(s) and Cs 2 Cr O 4 (s) have been evaluated by enthalpy-increment measurements, using a Calvet high-temperature calorimeter. Least squares analyses were performed on the enthalpy increment results. Data is presented in tabular form for the dependence of enthalpy increments on temperature, in the range 333 to 822 K, for both caesium compounds, along with the thermal properties of the compounds. Good agreement is found between the present data and previously reported results on reduced enthalpy increments of CsI(s) and Cs 2 CrO 4 (s). (U.K.)

Adobe Photoshop Elements 11 for photographers

CERN Document Server

Andrews, Philip

2013-01-01

To coincide with some of the biggest changes in Photoshop Elements for years, Philip Andrews completely revises his bestselling title to include all the new features of this release. See how the new interface works alongside new tools, techniques and workflows to make editing, enhancing and sharing your pictures easier than ever. And as always, he introduces the changed and improved features with colorful illustrations and the clear step-by-step instruction that has made his books the go-to titles for photographers the world over. ????In this edition Andrews highlights followi

Electrical behaviour of heterobimetallic [MM'(EtCS2)4] (MM'=NiPd, NiPt, PdPt) and MM'X-chain polymers [PtM(EtCS2)4I] (M=Ni, Pd).

Science.gov (United States)

Givaja, Gonzalo; Castillo, Oscar; Mateo, Eva; Gallego, Almudena; Gómez-García, Carlos J; Calzolari, Arrigo; di Felice, Rosa; Zamora, Félix

2012-11-26

Herein, we report the isolation of new heterobimetallic complexes [Ni(0.6)Pd(1.4)(EtCS(2))(4)] (1), [NiPt(EtCS(2))(4)] (2) and [Pd(0.4)Pt(1.6)(EtCS(2))(4)] (3), which were constructed by using transmetallation procedures. Subsequent oxidation with iodine furnished the MM'X monodimensional chains [Ni(0.6)Pt(1.4)(EtCS(2))(4)I] (4) and [Ni(0.1)Pd(0.3)Pt(1.6)(EtCS(2))(4)I] (5). The physical properties of these systems were investigated and the chain structures 4 and 5 were found to be reminiscent of the parent [Pt(2)(EtCS(2))(4)I] species. However, they were more sensitively dependent on the localised nature of the charge on the Ni ion, which caused spontaneous breaking of the conduction bands. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Efficient small-molecule organic solar cells incorporating a doped buffer layer

Energy Technology Data Exchange (ETDEWEB)

Chou, Dei-Wei [Department of aviation and Communication Electronics, Air Force Institute of Technology, Kaohsiung 820, Taiwan (China); Chen, Kan-Lin [Department of Electronic Engineering, Fortune Institute of Technology, Kaohsiung 831, Taiwan (China); Huang, Chien-Jung, E-mail: chien@nuk.edu.tw [Department of Applied Physics, National University of Kaohsiung, Nanzih, Kaohsiung 811, Taiwan (China); Tsao, Yao-Jen [Department of Applied Physics, National University of Kaohsiung, Nanzih, Kaohsiung 811, Taiwan (China); Chen, Wen-Ray; Meen, Teen-Hang [Department of Electronic Engineering, National Formosa University, Hu-Wei, Yunlin 632, Taiwan (China)

2013-06-01

Small-molecule organic solar cells (OSCs) with an optimized structure of indium tin oxide/poly (3,4-ethylenedioxythioxythiophene):poly(styrenesulfonate)/copper phthalocyanine (CuPc) (10 nm)/CuPc: fullerene (C{sub 60}) mixed (20 nm)/C{sub 60} (20 nm)/4,7-diphenyl-1,10-phenanthroline (BPhen) (5 nm)/Ag were fabricated. In this study, the cesium carbonate-doped BPhen (Cs{sub 2}CO{sub 3}:BPhen) was adopted as the buffer layer to enhance the efficiency of the OSCs. The photovoltaic parameters of the OSCs, such as the short-circuit current density and fill factor, depend on the doping concentration of Cs{sub 2}CO{sub 3} in the BPhen layer. The cell with a Cs{sub 2}CO{sub 3}:BPhen (1:4) cathode buffer layer exhibits a power conversion efficiency (PCE) of 3.51%, compared to 3.37% for the device with the pristine BPhen layer. The enhancement of PCE was attributed to the energy-level alignment between the C{sub 60} layer and the Cs{sub 2}CO{sub 3}:BPhen layer. In addition, the characterization measured using atomic force microscopy shows that the Cs{sub 2}CO{sub 3}:BPhen layers have smoother surfaces. - Highlight: • Cs2CO3-doped 4,7-diphenyl-1,10-phenanthroline (BPhen) cathode buffer layer. • Cs2CO3:BPhen layer with different ratios affects organic solar cells performance. • Cell with 1:4 (Cs2CO3:BPhen) ratio shows 3.51% power conversion efficiency.

Fission product behavior in high-temperature water: CsI vs MoO4

Science.gov (United States)

Kanjana, K.; Silva, K.; Channuie, J.

2017-09-01

Fission product behaviors of Cs, a major element released in a severe nuclear accident, still remain unclear. The question frequently addressed is whether Cs released will be in the form of Cs2MoO4 or CsOH. This is a challenging issue since it has been demonstrated that the reaction between Cs2MoO4 and water leading to CsOH production is thermodynamically favored. The present research aims at investigation of CsOH generation through this chemical channel. A high-temperature setup with a flow system based on the cooling system of a water-cooled nuclear reactor has been assembled. The reaction between aqueous solutions of CsI and Na2MoO4 in a high-corrosion-resistant hot cell (Hastelloy) has been studied up to 80 °C in deoxygenated system. The products have been characterized using FTIR and XRD. The results have shown that there is no reaction between CsI and Na2MoO4 under the experimental conditions.

Coprecipitation of 137Cs and 85Sr microquantities with complex compound [M(18-crown-6)]BPH4 (M=Na+, Cs+) from neutral and alkaline solutions

International Nuclear Information System (INIS)

Konovalova, N.A.; Rumer, I.A.; Kulyukhin, S.A.

2009-01-01

The paper reports the possibility of joint separation of 137 Cs and 85 Sr from neutral and alkaline aqueous solutions by their coprecipitation with the solid phase of complex compounds [M(18-crown-6)]BPh 4 (M=Na + , Cs + ), as well as to study the coprecipitation of 137 Cs and 85 Sr with the solid phase CsBPh 4 . It is found that complex compounds [M(18-crown-6)]BPh 4 (M=Na + , Cs + ) increased the degree of 85 Sr separation from solutions virtually two- to threefold vs. CsBPh 4 . Chloride and nitrate were found to have hardly any impact on the coprecipitation of 137 Cs and 85 Sr with [M(18-crown-6)]BPh 4 (M = Na + , Cs + ). (orig.)

Two structure types based on Si6O15 rings: synthesis and structural and spectroscopic characterisation of Cs1.86K1.14DySi6O15 and Cs1.6K1.4SmSi6O15

International Nuclear Information System (INIS)

Wierzbicka-Wieczorek, Maria; Goeckeritz, Martin; Kolitsch, Uwe; Lenz, Christoph; Giester, Gerald

2015-01-01

The silicate Cs 1.86 K 1.14 DySi 6 O 15 represents a mixed tetrahedral-octahedral framework structure type based on roughly circular Si 6 O 15 rings and isolated DyO 6 octahedra. The silicate Cs 1.6 K 1.4 SmSi 6 O 15 has a layered atomic arrangement built from corrugated Si 6 O 15 layers containing four-, six- and eight-membered rings. The layers are connected by isolated SmO 6 octahedra to form a mixed tetrahedral-octahedral framework. This structure shows a close structural relationship to β-K 3 NdSi 6 O 15 and a less close one to dehydrated elpidite (Na 2 ZrSi 6 O 15 ). In both structures, Cs/K atoms occupy large voids. The silicates were obtained through high-temperature flux syntheses. Their crystal structures have been determined from single-crystal X-ray diffraction data. Cs 1.86 K 1.14 DySi 6 O 15 crystallises in R32 (no. 155) with a = 13.896(2), c = 35.623(7) Aa and V = 5957.2(17) Aa 3 , whereas Cs 1.6 K 1.4 SmSi 6 O 15 crystallises in Cmca (no. 64) with a = 14.474(3), b = 14.718(3), c = 15.231(3) Aa and V = 3244.7(11) Aa 3 . The Dy 3+ and Sm 3+ cations present in the silicates cause PL emission bands in the visible yellow-to-orange spectral range. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Foundation Fireworks CS4

CERN Document Server

Smith, N; Heerema, Matt; Mallott, Chuch; King, R; Erskine, Craig

2009-01-01

Are you a web designer who is looking for a new and quicker way to prototype and create for the web? Perhaps you are a programmer who finds most design tools to be overkill for what you need to get done. Or, maybe you're an old Fireworks pro, who wants to keep up to date on the latest changes in Creative Suite 4. Either way, this book has something for you. * Coverage of all that's new and powerful for the Web designer and developer in Fireworks CS4* Targets developers who want design tools that don't get in their way and designers who want development tools that don't constrain their creativi

Solution-Grown CsPbBr3 /Cs4 PbBr6 Perovskite Nanocomposites: Toward Temperature-Insensitive Optical Gain.

Science.gov (United States)

Wang, Yue; Yu, Dejian; Wang, Zeng; Li, Xiaoming; Chen, Xiaoxuan; Nalla, Venkatram; Zeng, Haibo; Sun, Handong

2017-09-01

With regards to developing miniaturized coherent light sources, the temperature-insensitivity in gain spectrum and threshold is highly desirable. Quantum dots (QDs) are predicted to possess a temperature-insensitive threshold by virtue of the separated electronic states; however, it is never observed in colloidal QDs due to the poor thermal stability. Besides, for the classical II-VI QDs, the gain profile generally redshifts with increasing temperature, plaguing the device chromaticity. Herein, this paper addresses the above two issues simultaneously by embedding ligands-free CsPbBr 3 nanocrystals in a wider band gap Cs 4 PbBr 6 matrix by solution-phase synthesis. The unique electronic structures of CsPbBr 3 nanocrystals enable temperature-insensitive gain spectrum while the lack of ligands and protection from Cs 4 PbBr 6 matrix ensure the thermal stability and high temperature operation. Specifically, a color drift-free stimulated emission irrespective of temperature change (20-150 °C) upon two-photon pumping is presented and the characteristic temperature is determined to be as high as ≈260 K. The superior gain properties of the CsPbBr 3 /Cs 4 PbBr 6 perovskite nanocomposites are directly validated by a vertical cavity surface emitting laser operating at temperature as high as 100 °C. The results shed light on manipulating optical gain from the advantageous CsPbBr 3 nanocrystals and represent a significant step toward the temperature-insensitive frequency-upconverted lasers. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Phase diagram of the CsH/sub 2/AsO/sub 4/-CsH /SUB 0. 1/ D /SUB 1. 9/ AsO/sub 4/ System

Energy Technology Data Exchange (ETDEWEB)

Rakhimov, K.; Karapetyan, F.S.; Kozhenkov, V.Y.; Polyakov, Y.A.; Zhigarnovskii, B.M.

1986-05-01

The authors determined the melting point of dueterated cesium hydrogen arsenate of composition CsH /SUB 0.1/ D /SUB 1.9/ AsO/sub 4/ melts. Specimens for investigation of the system were prepared by fusion of appropriate amounts of CsH/sub 2/AsO/sub 4/ and CsH /SUB 0.1/ D /SUB 1.9/ AsO/sub 4/ in sealed quartz ampuls. In addition, the unit-cell parameters of the phases of the specimens practically did not differ from the corresponding parameters of the starting products over the entire range of concentrations.

Photoshop Elements 9 the missing manual

CERN Document Server

Brundage, Barbara

2010-01-01

Elements 9 offers much of Photoshop's power without the huge price tag. It's an ideal tool for most image-editing buffs -- including scrapbookers, photographers, and aspiring graphic artists. But Elements still doesn't come with a decent manual. This bestselling book will help you get the most out of the program, from the basics to advanced tips for both Windows and Mac. Quickly learn your way around. Customize Elements to suit your working style.Get to work right away. Import, organize, and make quick image fixes with ease.Retouch any image. Learn how to repair and restore your old and damag

How to cheat in Photoshop CC

CERN Document Server

Caplin, Steve

2013-01-01

Have you ever struggled to make the vision in your mind come to life on your screen? Then this book can help you realise your goal. In this comprehensive revision of the best-selling How To Cheat in Photoshop, photomontage guru Steve Caplin shows you how to get optimum results in minimum time, by cheating your way to success.As a professional digital artist, Steve knows all about creating great work under pressure. In this book he combines detailed step-by-step instructions with invaluable real-world hints, tips, and advice to really let your creativity run wild. Fully updated to

Photoshop Elements 10 The Missing Manual

CERN Document Server

Brundage, Barbara

2011-01-01

Elements 10 offers much of Photoshop's power without the huge price tag. It's a great tool for most image-editing buffs-whether you're a photographer, scrapbooker, or aspiring graphic artist. But Elements still doesn't come with a useful manual. This bestselling book helps you get the most out of the program, from the basics to advanced tips for both Windows and Mac users. The important stuff you need to know: Quickly learn your way around. Customize Elements to suit your working style.Get to work right away. Import, organize, and make quick image fixes with ease.Retouch any image. Learn how

A novel method for measuring anterior segment area of the eye on ultrasound biomicroscopic images using photoshop.

Science.gov (United States)

Wang, Zhonghao; Liang, Xuanwei; Wu, Ziqiang; Lin, Jialiu; Huang, Jingjing

2015-01-01

To describe a novel method for quantitative measurement of area parameters in ocular anterior segment ultrasound biomicroscopy (UBM) images using Photoshop software and to assess its intraobserver and interobserver reproducibility. Twenty healthy volunteers with wide angles and twenty patients with narrow or closed angles were consecutively recruited. UBM images were obtained and analyzed using Photoshop software by two physicians with different-level training on two occasions. Borders of anterior segment structures including cornea, iris, lens, and zonules in the UBM image were semi-automatically defined by the Magnetic Lasso Tool in the Photoshop software according to the pixel contrast and modified by the observers. Anterior chamber area (ACA), posterior chamber area (PCA), iris cross-section area (ICA) and angle recess area (ARA) were drawn and measured. The intraobserver and interobserver reproducibilities of the anterior segment area parameters and scleral spur location were assessed by limits of agreement, coefficient of variation (CV), and intraclass correlation coefficient (ICC). All of the parameters were successfully measured by Photoshop. The intraobserver and interobserver reproducibilities of ACA, PCA, and ICA were good, with no more than 5% CV and more than 0.95 ICC, while the CVs of ARA were within 20%. The intraobserver and interobserver reproducibilities for defining the spur location were more than 0.97 ICCs. Although the operating times for both observers were less than 3 minutes per image, there was significant difference in the measuring time between two observers with different levels of training (pPhotoshop showed good intraobserver and interobserver reproducibilties. The methodology was easy to adopt and effective in measuring.

Luminescent CsPbI.sub.3./sub. and Cs.sub.4./sub.PbI.sub.6./sub. aggregates in annealed CsI:Pb crystals

Czech Academy of Sciences Publication Activity Database

Babin, V.; Fabeni, P.; Nikl, Martin; Nitsch, Karel; Pazzi, G.P.; Zazubovich, S.

2001-01-01

Roč. 226, č. 2 (2001), s. 419-428 ISSN 0370-1972 Institutional research plan: CEZ:AV0Z1010914 Keywords : CsPbI 3 * Cs 4 PbI 6 * nanoaggregates * luminescence Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.873, year: 2001

An investigation of the thermal conductivity of Cs2MoO4

International Nuclear Information System (INIS)

Ishii, T.; Mizuno, T.

1997-01-01

The thermal diffusivity of 82.6% TD and 89.3% TD Cs 2 MoO 4 was measured by the laser flash method and the thermal conductivity was calculated. The thermal conductivity of these Cs 2 MoO 4 ranged from 0.3 to 0.5 W m -1 K -1 . The density dependence of the thermal conductivity was correlated based on the experimental values of these two densities and on the 94.3% TD specimen from the preceding study. The correlation of the thermal conductivity of Cs 2 MoO 4 is k=(1.0-1.848 x P)/(1.0-1.848 x P ref ) x k ref , where k ref =132.56/T+0.03+3.2 x 10 -10 x T 3 , P ref =1.0-0.943=0.057 and k and k ref are the thermal conductivities (Wm -1 K -1 ) of Cs 2 MoO 4 with the porosities P and P ref , respectively, where P ref is the porosity for the 94.3% TD Cs 2 MoO 4 . T is the temperature (K). This correlation is applicable for 82.6 to 94.3% TD Cs 2 MoO 4 from 873 to 1023 K. (orig.)

Elastic properties of Cs{sub 2}HgBr{sub 4} and Cs{sub 2}CdBr{sub 4} crystals

Energy Technology Data Exchange (ETDEWEB)

Kityk, A.V.; Zadorozhna, A.V.; Shchur, Y.I.; Martynyuk-Lototska, Y.I.; Burak, Y.; Vlokh, O.G. [Institute of Physical Optics, Lvov (Ukraine)

1998-12-31

Using ultrasonic velocity measurements, all components of the elastic constant matrix C{sub ij} , elastic compliances matrix S{sub ij}, and linear compressibility constants matrix K{sub ij} of orthorhombic Cs{sub 2}HgBr{sub 4} and Cs{sub 2}CdBr{sub 4} crystals have been determined over a wide temperature range, including the region of the phase transition from the normal to the incommensurate phase. Results obtained are considered within the framework of the phenomenological theory. Preliminary analysis of the acoustical properties at room temperature clearly indicates that both crystals are relatively important materials for acousto-optical applications. Copyright (1998) CSIRO Australia 16 refs., 1 tab. 8 figs. The URL for the electronic version of this article is http://www.publish.csiro.au/journals/ajp/electronic.html

Antibodies derived from an enterotoxigenic Escherichia coli (ETEC) adhesin tip MEFA (multiepitope fusion antigen) against adherence of nine ETEC adhesins: CFA/I, CS1, CS2, CS3, CS4, CS5, CS6, CS21 and EtpA.

Science.gov (United States)

Nandre, Rahul M; Ruan, Xiaosai; Duan, Qiangde; Sack, David A; Zhang, Weiping

2016-06-30

Diarrhea continues to be a leading cause of death in children younger than 5 years in developing countries. Enterotoxigenic Escherichia coli (ETEC) is a leading bacterial cause of children's diarrhea and travelers' diarrhea. ETEC bacteria initiate diarrheal disease by attaching to host receptors at epithelial cells and colonizing in small intestine. Therefore, preventing ETEC attachment has been considered the first line of defense against ETEC diarrhea. However, developing vaccines effectively against ETEC bacterial attachment encounters challenge because ETEC strains produce over 23 immunologically heterogeneous adhesins. In this study, we applied MEFA (multiepitope fusion antigen) approach to integrate epitopes from adhesin tips or adhesive subunits of CFA/I, CS1, CS2, CS3, CS4, CS5, CS6, CS21 and EtpA adhesins and to construct an adhesin tip MEFA peptide. We then examined immunogenicity of this tip MEFA in mouse immunization, and assessed potential application of this tip MEFA for ETEC vaccine development. Data showed that mice intraperitoneally immunized with this adhesin tip MEFA developed IgG antibody responses to all nine ETEC adhesins. Moreover, ETEC and E. coli bacteria expressing these nine adhesins, after incubation with serum of the immunized mice, exhibited significant reduction in attachment to Caco-2 cells. These results indicated that anti-adhesin antibodies induced by this adhesin tip MEFA blocked adherence of the most important ETEC adhesins, suggesting this multivalent tip MEFA may be useful for developing a broadly protective anti-adhesin vaccine against ETEC diarrhea. Copyright © 2016 Elsevier Ltd. All rights reserved.

Efficient CsF interlayer for high and low bandgap polymer solar cell

Science.gov (United States)

Mitul, Abu Farzan; Sarker, Jith; Adhikari, Nirmal; Mohammad, Lal; Wang, Qi; Khatiwada, Devendra; Qiao, Qiquan

2018-02-01

Low bandgap polymer solar cells have a great deal of importance in flexible photovoltaic market to absorb sun light more efficiently. Efficient wide bandgap solar cells are always available in nature to absorb visible photons. The development and incorporation of infrared photovoltaics (IR PV) with wide bandgap solar cells can improve overall solar device performance. Here, we have developed an efficient low bandgap polymer solar cell with CsF as interfacial layer in regular structure. Polymer solar cell devices with CsF shows enhanced performance than Ca as interfacial layer. The power conversion efficiency of 4.5% has been obtained for PDPP3T based polymer solar cell with CsF as interlayer. Finally, an optimal thickness with CsF as interfacial layer has been found to improve the efficiency in low bandgap polymer solar cells.

A novel method for measuring anterior segment area of the eye on ultrasound biomicroscopic images using photoshop.

Directory of Open Access Journals (Sweden)

Zhonghao Wang

Full Text Available To describe a novel method for quantitative measurement of area parameters in ocular anterior segment ultrasound biomicroscopy (UBM images using Photoshop software and to assess its intraobserver and interobserver reproducibility.Twenty healthy volunteers with wide angles and twenty patients with narrow or closed angles were consecutively recruited. UBM images were obtained and analyzed using Photoshop software by two physicians with different-level training on two occasions. Borders of anterior segment structures including cornea, iris, lens, and zonules in the UBM image were semi-automatically defined by the Magnetic Lasso Tool in the Photoshop software according to the pixel contrast and modified by the observers. Anterior chamber area (ACA, posterior chamber area (PCA, iris cross-section area (ICA and angle recess area (ARA were drawn and measured. The intraobserver and interobserver reproducibilities of the anterior segment area parameters and scleral spur location were assessed by limits of agreement, coefficient of variation (CV, and intraclass correlation coefficient (ICC.All of the parameters were successfully measured by Photoshop. The intraobserver and interobserver reproducibilities of ACA, PCA, and ICA were good, with no more than 5% CV and more than 0.95 ICC, while the CVs of ARA were within 20%. The intraobserver and interobserver reproducibilities for defining the spur location were more than 0.97 ICCs. Although the operating times for both observers were less than 3 minutes per image, there was significant difference in the measuring time between two observers with different levels of training (p<0.001.Measurements of ocular anterior segment areas on UBM images by Photoshop showed good intraobserver and interobserver reproducibilties. The methodology was easy to adopt and effective in measuring.

Digitally quantifying cerebral hemorrhage using Photoshop and Image J.

Science.gov (United States)

Tang, Xian Nan; Berman, Ari Ethan; Swanson, Raymond Alan; Yenari, Midori Anne

2010-07-15

A spectrophotometric hemoglobin assay is widely used to estimate the extent of brain hemorrhage by measuring the amount of hemoglobin in the brain. However, this method requires using the entire brain sample, leaving none for histology or other assays. Other widely used measures of gross brain hemorrhage are generally semi-quantitative and can miss subtle differences. Semi-quantitative brain hemorrhage scales may also be subject to bias. Here, we present a method to digitally quantify brain hemorrhage using Photoshop and Image J, and compared this method to the spectrophotometric hemoglobin assay. Male Sprague-Dawley rats received varying amounts of autologous blood injected into the cerebral hemispheres in order to generate different sized hematomas. 24h later, the brains were harvested, sectioned, photographed then prepared for the hemoglobin assay. From the brain section photographs, pixels containing hemorrhage were identified by Photoshop and the optical intensity was measured by Image J. Identification of hemorrhage size using optical intensities strongly correlated to the hemoglobin assay (R=0.94). We conclude that our method can accurately quantify the extent of hemorrhage. An advantage of this technique is that brain tissue can be used for additional studies. Published by Elsevier B.V.

Quantification of video-taped images in microcirculation research using inexpensive imaging software (Adobe Photoshop).

Science.gov (United States)

Brunner, J; Krummenauer, F; Lehr, H A

2000-04-01

Study end-points in microcirculation research are usually video-taped images rather than numeric computer print-outs. Analysis of these video-taped images for the quantification of microcirculatory parameters usually requires computer-based image analysis systems. Most software programs for image analysis are custom-made, expensive, and limited in their applicability to selected parameters and study end-points. We demonstrate herein that an inexpensive, commercially available computer software (Adobe Photoshop), run on a Macintosh G3 computer with inbuilt graphic capture board provides versatile, easy to use tools for the quantification of digitized video images. Using images obtained by intravital fluorescence microscopy from the pre- and postischemic muscle microcirculation in the skinfold chamber model in hamsters, Photoshop allows simple and rapid quantification (i) of microvessel diameters, (ii) of the functional capillary density and (iii) of postischemic leakage of FITC-labeled high molecular weight dextran from postcapillary venules. We present evidence of the technical accuracy of the software tools and of a high degree of interobserver reliability. Inexpensive commercially available imaging programs (i.e., Adobe Photoshop) provide versatile tools for image analysis with a wide range of potential applications in microcirculation research.

137Cs in a raised bog in central Sweden

International Nuclear Information System (INIS)

Rosen, K.; Vinichuk, M.; Johanson, K.J.

2009-01-01

The vertical distribution of 137 Cs activity in peat soil profiles and 137 Cs activity concentration in plants of various species was studied in samples collected at two sites on a raised bog in central Sweden. One site (open bog) was in an area with no trees and only a few sparsely growing plant species, while the other (low pine) was less than 100 m from the open bog site and had slowly growing Scots pine, a field layer dominated by some ericaceous plants and ground well-covered by plants. The plant samples were collected in 2004-2007 and were compared with samples collected in 1989 from the same open bog and low pine sites. Ground deposition of 137 Cs in 2005 was similar at both sites, 23 000 Bq m -2 . In the open bog peat profile it seems to be an upward transport of caesium since a clear peak of 137 Cs activity was found in the uppermost 1-4 cm of Sphagnum layers, whereas at the low pine site 137 Cs was mainly found in deeper (10-12 cm) layers. The migration rate was 0.57 cm yr -1 at the open bog site and the migration centre of 137 Cs was at a depth of 10.7, while the rate at the low pine site was 0.78 cm yr -1 and the migration centre was at 14.9 cm. Heather (Calluna vulgaris) was the plant species with the highest 137 Cs activity concentrations at both sites, 43.5 k Bq -1 DM in 1989 decreasing to 20.4 in 2004-2007 on open bog and 22.3 k Bq kg -1 DM in 1989 decreasing to 11.2 k Bq -1 DM by the period 2004-2007 on the low pine site. 137 Cs transfer factors in plants varied between 0.88 and 1.35 on the open bog and between 0.48 and 0.69 m 2 kg -1 DM at the low pine site.

Flash CS4: The Missing Manual

CERN Document Server

Grover, Chris

2008-01-01

Unlock the power of Flash and bring gorgeous animations to life onscreen. Flash CS4: The Missing Manual includes a complete primer on animation, a guided tour of the program's tools and capabilities, lots of new illustrations, and more details on working with video. Beginners will learn to use the software in no time, and experienced Flash designers will improve their skills.

The Cs2SO4-Ce2(SO4)3-H2SO4-H2O system at 150 and 200 deg C

International Nuclear Information System (INIS)

Bondar', S.A.; Belokoskov, V.I.; Trofimov, G.V.

1982-01-01

Solubility in the system Cs 2 SO 4 -Ce 2 (SO 4 ) 3 -H 2 SO 4 -H 2 O using the isothermal method at 150 and 200 deg C at molar ratios Cs 2 SO 4 :Ce 2 (SO 4 ) 3 =1:5 and conditions of sulfate crystallization Cs 2 SO 4 xCe 2 (SO 4 ) 3 , Ce 2 (SO 4 ) 3 x0.5H 2 SO 4 xnH 2 O (n=2-3) and Ce 2 (SO 4 ) 3 x3H 2 SO 4 are determined. Double sulfate Cs 2 SO 4 xCe 2 (SO 4 ) 3 is studied using the methods of crystallooptical, thermal, X-ray phase analyses and IR spectroscopy

Room-temperature synthesis of pure perovskite-related Cs4PbBr6 nanocrystals and their ligand-mediated evolution into highly luminescent CsPbBr3 nanosheets

Science.gov (United States)

Yang, Liu; Li, Dongmei; Wang, Cong; Yao, Wei; Wang, Hao; Huang, Kaixiang

2017-07-01

Currently, all-inorganic cesium lead-halide perovskite nanocrystals have attracted enormous attentions owing to their excellent optical performances. While great efforts have been devoted to CsPbBr3 nanocrystals, the perovskite-related Cs4PbBr6 nanocrystals, which were newly reported, still remained poorly understood. Here, we reported a novel room-temperature reaction strategy to synthesize pure perovskite-related Cs4PbBr6 nanocrystals. Size of the products could be adjusted through altering the amount of ligands, simply. A mixture of two good solvents with different polarity was innovatively used as precursor solvent, being one key to the high-yield Cs4PbBr6 nanocrystals synthesis. Other two keys were Cs+ precursor concentration and surface ligands. Ingenious experiments were designed to reveal the underlying reaction mechanism. No excitonic emission was observed from the prepared Cs4PbBr6 nanocrystals in our work. We considered the green emission which was observed in other reports originated from the avoidless transformation of Cs4PbBr6 into CsPbBr3 nanocrystals. Indeed, the new-prepared Cs4PbBr6 nanocrystals could transform into CsPbBr3 nanosheets with surface ligands mediated. The new-transformed two-dimensional CsPbBr3 nanosheets could evolve into large-size nanosheets. The influences of surface ligand density on the fluorescent intensity and stability of transformed CsPbBr3 nanosheets were also explained. Notably, the photoluminescence quantum yield of the as-transformed CsPbBr3 nanosheets could reach as high as 61.6% in the form of thin film. The fast large-scale synthesis of Cs4PbBr6 nanocrystals and their ligand-mediated transformation into high-fluorescent CsPbBr3 nanosheets will be beneficial to the future optoelectronic applications. Our work provides new approaches to understand the structural evolution and light-emitting principle of perovskite nanocrystals. [Figure not available: see fulltext.

Game Art Complete All-in-One; Learn Maya, 3ds Max, ZBrush, and Photoshop Winning Techniques

CERN Document Server

Gahan, Andrew

2008-01-01

A compilation of key chapters from the top Focal game art books available today - in the areas of Max, Maya, Photoshop, and ZBrush. The chapters provide the CG Artist with an excellent sampling of essential techniques that every 3D artist needs to create stunning game art. Game artists will be able to master the modeling, rendering, rigging, and texturing techniques they need - with advice from Focal's best and brightest authors. Artists can learn hundreds of tips, tricks and shortcuts in Max, Maya, Photoshop, ZBrush - all within the covers of one complete, inspiring reference

Structural study of caesium-based britholites Sr7La2Cs(PO4)5(SiO4)F2

International Nuclear Information System (INIS)

Boughzala, K.; Gmati, N.; Bouzouita, K.; Ben Cherifa, A.; Gravereau, P.

2010-01-01

Several studies demonstrated the ability of britholites to retain radionuclides such as the caesium and actinides. Therefore, three compounds with formulas Sr 8 LaCs(PO 4 ) 6 F 2 , Sr 7 La 2 Cs(PO 4 ) 5 (SiO 4 )F 2 and Sr 2 La 7 Cs(SiO 4 ) 6 F 2 , were prepared by solid state reaction. However, it seems that only the mono-silicated composition was obtained in a pure state. In this present work, the X-ray diffraction and magnetic nuclear resonance have been used to investigate the structure for this composition. The results showed that in fact this phase was not pure, but it was mixed with a secondary phase, SrLaCs(PO 4 ) 2 . The refinement by the Rietveld method allowed also to precise the distribution of La 3+ and Cs + ions between the two cationic sites of the apatite. (authors)

Enhancing Architectural Drawings and Models with Photoshop

CERN Document Server

Onstott, Scott

2010-01-01

Transform your CAD drawings into powerful presentationThis one-of-a-kind book shows you how to use Photoshop to turn CAD drawings and BIM models into artistic presentations with captivating animations, videos, and dynamic 3D imagery. The techniques apply to all leading architectural design software including AutoCAD, Revit, and 3ds Max Design. Video tutorials on the DVD improve your learning curve and let you compare your work with the author's.Turn CAD drawings and BIM models into powerful presentations featuring animation, videos, and 3D imagery for enhanced client appealCraft interactive pa

Volatility of components of saturated vapours of UCl4-CsCl and UCl4-LiCl molten mixtures

International Nuclear Information System (INIS)

Smirnov, M.V.; Kudyakov, V.Ya.; Salyulev, A.B.; Komarov, V.E.; Posokhin, Yu.V.; Afonichkin, V.K.

1979-01-01

The flow method has been used for measuring the volatility of the components from UCl 4 -CsCl and UCl 4 -LiCl melted mixtures containing 2.0, 5.0, 12.0, 25.0, 33.0, 50.0, 67.0, and 83.0 mol.% of UCl 4 within the temperature ranges of 903-1188 K and 740-1200 K, respectively. The chemical composition of saturated vapours above the melted salts has been determined. The melted mixtures in question exhibit negative deviation from ideal behaviour. Made was the conclusion about the presence in a vapour phase, along with monomeric UCl 4 , LiCl, CsCl and Li 2 Cl 2 , Cs 2 Cl 2 dimers of double compounds of the MeUCl 5 most probable composition. Their absolute contribution into a total pressure above the UCl 4 -CsCl melted mixtures is considerably smaller than above the UCl 4 -LiCl mixtures

Differentiation between chronic hepatitis and normal liver of grayscale ultrasound tissue quantification using adobe photoshop(5.0)

International Nuclear Information System (INIS)

Choi, Jong Cheol; Oh, Jong Young; Lim, Jong Uk; Nam, Kyung Jin

2001-01-01

To evaluate whether was any difference in the brightness of echogenicity on gray scale ultrasound imaging between the liver with chronic hepatitis and the normal liver using Adobe photoshop 5.0 Seventy-five patients with pathologically proven chronic hepatitis and twenty normal volunteers were included in this study. Adobe photoshop 5.0 histogram was used to measure the brightness of image. The measured brightness of the liver was divided by the brightness of the kidney, and the radio was calculated and compared between patients with chronic hepatitis and the normal control groups. In addition, the degree of fibrosis was also evaluated. The difference in brightness between the normal liver and live with chronic hepatitis was statistically significant, but no statistically significant difference was observed between the brightness of the liver and the degree of fibrosis in the liver. Tissue echo quantification using Adobe Photoshop 5.0 may be a helpful diagnostic methods for the patients with chronic hepatitis.

133Cs NMR investigation of 2D frustrated Heisenberg antiferromagnet, Cs2CuCl4

Science.gov (United States)

Vachon, M.-A.; Kundhikanjana, W.; Straub, A.; Mitrovic, V. F.; Reyes, A. P.; Kuhns, P.; Coldea, R.; Tylczynski, Z.

2006-10-01

We report 133Cs nuclear magnetic resonance (NMR) measurements on the 2D frustrated Heisenberg antiferromagnet Cs2CuCl4 down to 2 K and up to 15 T. We show that 133Cs NMR is a good probe of the magnetic degrees of freedom in this material. Cu spin degrees of freedom are sensed through a strong anisotropic hyperfine coupling. The spin excitation gap opens above the critical saturation field. The gap value was determined from the activation energy of the nuclear spin-lattice relaxation rate in a magnetic field applied parallel to the Cu chains (\\skew3\\hat{b} axis). The values of the g-factor and the saturation field are consistent with the neutron-scattering and magnetization results. The measurements of the spin spin relaxation time are exploited to show that no structural changes occur down to the lowest temperatures investigated.

Crystal structure of 4-RbHo(PO3)4, 4-RbTm(PO3)4 and 4-CsEr(PO3)4

International Nuclear Information System (INIS)

Maksimova, S.I.; Palkina, K.K.; Chibiskova, N.T.

1982-01-01

X-ray structural study of 4-RbLn(PO 3 ) 4 (Ln=Mo, Tm) and 4-CsEr(PO 3 ) 4 is carried out. The compounds are crystallized in monoclinic crystal system, sp. gr P2 1 /n. Parameters of their unit cell, atom coordinates, anisotropic heat parameters, interatomic distances and valent angles are given. 4-RbHo(PO 3 ) 4 , 4-RbTm(PO 3 ) 4 , 4-CsEr(PO 3 ) 4 are isostructural to previously studied TlNd(PO 3 ) and 4-RbNd(PO 3 ) 4 . Using as an example the structural type 4-M 1 Ln(PO 3 ) 4 it is shown that the change of the shortest distances Ln-Ln, M 1 -M 1 and M 1 -Ln, as well as of degree of polymorphous chain corrugation to a higher extent depends on rare earth atom dimensions, than on monovalent metal ion dimensions [ru

Facile synthesis of NaYF4:Yb, Ln/NaYF4:Yb core/shell upconversion nanoparticles via successive ion layer adsorption and one-pot reaction technique

NARCIS (Netherlands)

Zeng, Q.; Xue, B.; Zhang, Y.; Wang, D.; Liu, X.; Tu, L.; Zhao, H.; Kong, X.; Zhang, H.

2013-01-01

The facile one-pot synthesis of NaYF4:Yb, Ln/NaYF4:Yb core/shell (CS) upconversion nanoparticles (UCNPs) was firstly developed through the successive ion layer adsorption and reaction (SILAR) technique, which represents an attractive alternative to conventional synthesis utilizing the chloride of Ln

Single crystal growth, electronic structure and optical properties of Cs2HgBr4

Science.gov (United States)

Lavrentyev, A. A.; Gabrelian, B. V.; Vu, V. T.; Shkumat, P. N.; Parasyuk, O. V.; Fedorchuk, A. O.; Khyzhun, O. Y.

2015-10-01

We report on successful synthesis of high-quality single crystal of cesium mercury tetrabromide, Cs2HgBr4, by using the vertical Bridgman-Stockbarger method as well as on studies of its electronic structure. For the Cs2HgBr4 crystal, we have recorded X-ray photoelectron spectra for both pristine and Ar+ ion-bombarded surfaces. Our data indicate that the Cs2HgBr4 single crystal surface is rather sensitive with respect to Ar+ ion-bombardment. In particular, such a treatment of the Cs2HgBr4 single crystal surface alters its elemental stoichiometry. To explore peculiarities of the energy distribution of total and partial densities of states within the valence band and the conduction band of Cs2HgBr4, we have made band-structure calculations based on density functional theory (DFT) employing the augmented plane wave+local orbitals (APW+lo) method as incorporated in the WIEN2k package. The APW+lo calculations allow for concluding that the Br 4p states make the major contributions in the upper portion of the valence band, while its lower portion is dominated by contributors of the Hg 5d and Cs 5p states. Further, the main contributors to the bottom of the conduction band of Cs2HgBr4 are the unoccupied Br p and Hg s states. In addition, main optical characteristics of Cs2HgBr4 such as dispersion of the absorption coefficient, real and imaginary parts of dielectric function, electron energy-loss spectrum, refractive index, extinction coefficient and optical reflectivity have been explored from the first-principles band-structure calculations.

Cs[FeSe{sub 2}], Cs{sub 3}[FeSe{sub 2}]{sub 2}, and Cs{sub 7}[Fe{sub 4}Se{sub 8}]. Missing links of known chalcogenido ferrate series

Energy Technology Data Exchange (ETDEWEB)

Stueble, Pirmin; Roehr, Caroline [Institut fuer Anorganische und Analytische Chemie, Universitaet Freiburg (Germany)

2017-11-17

The three cesium selenido ferrate title compounds with an Se:Fe ratio of 2:1 were synthesized from stoichiometric samples reacting elemental Cs either (A) with Fe and Se in a double-crucible setup (Cs[FeSe{sub 2}], Cs{sub 3}[FeSe{sub 2}]{sub 2}) or (B) with previously prepared FeSe{sub 2} (Cs{sub 3}[FeSe{sub 2}]{sub 2}, Cs{sub 7}[Fe{sub 4}S{sub 8}]) (T{sub max} = 800-1000 C). The pure Fe{sup III} ferrate Cs[FeSe{sub 2}] crystallizes in the Tl[FeSe{sub 2}] type [monoclinic, space group C2/m, a = 1392.95(10), b = 564.43(3), c = 737.44(6) pm, β = 119.163(5) , Z = 4, R{sub 1} = 0.0550]. It is thus not isotypic to all other alkali ferrates(III) A[FeS{sub 2}] and A[FeSe{sub 2}] containing chains of edge-sharing tetrahedra, but crystallizes in a t2 subgroup of the Immm structure of Cs[FeS{sub 2}]. The mixed-valent chain compound Cs{sub 3}[FeSe{sub 2}]{sub 2} is isotypic to its sulfido analogue [orthorhombic, space group Pnma, a = 777.88(6), b = 1151.02(6), c = 1341.61(7) pm, Z = 4, R{sub 1} = 0.0470]. In contrast to the isopunctal Na{sub 3}[FeSe{sub 2}]{sub 2} type K/Rb compounds the chains are only slightly corrugated. The monoclinic, likewise mixed-valent Fe{sup II/III} selenido ferrate Cs{sub 7}[Fe{sub 4}Se{sub 8}] [monoclinic, space group C2/c, a = 1953.79(10), b = 879.71(5), c = 1717.03(10) pm, β = 117.890(2) , Z = 4, R{sub 1} = 0.0816] is isostructural both to the cesium sulfido and tellurido compound. The structure contains oligomeric moieties of four edge sharing [FeSe{sub 4}] tetrahedra forming slightly distorted tetrahedral clusters [Fe{sub 4}Se{sub 8}]{sup 7-}, which are surrounded by a cube of 26 Cs cations. Based on a structure map, the crystal chemistry of the three title compounds is discussed together with all chain/cluster ferrates of the general series A{sub 1+x}[Fe{sup III}{sub 1-x}Fe{sup II}{sub x}Q{sub 2}] (x = 0-1; A = Na, K, Rb, Cs; Q = S, Se, Te). (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Design and construction of a multi-layer CsI(Tl) telescope for high-energy reaction studies

International Nuclear Information System (INIS)

Yan, D.; Sun, Z.Y.; Yue, K.; Wang, S.T.; Zhang, X.H.; Yu, Y.H.; Chen, J.L.; Tang, S.W.; Fang, F.; Zhou, Y.; Sun, Y.; Wang, Z.M.; Sun, Y.Z.

2017-01-01

A prototype of a new CsI(Tl) telescope, which will be used in the reaction studies of light isotopes with energy of several hundred AMeV, was constructed and tested at the Institute of Modern Physics, Chinese Academy of Sciences. The telescope has a multi-layer structure, and the range information was obtained to improve the particle identification performance. This prototype has seven layers of different thickness. An energy resolution of 5.0% (FWHM) was obtained for one of the layers in a beam test experiment. Positive improvement for the identification of 14 O and 15 O isotopes was achieved using the range information.

Design and construction of a multi-layer CsI(Tl) telescope for high-energy reaction studies

Energy Technology Data Exchange (ETDEWEB)

Yan, D.; Sun, Z.Y. [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Yue, K., E-mail: yueke@impcas.ac.cn [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Wang, S.T.; Zhang, X.H.; Yu, Y.H.; Chen, J.L.; Tang, S.W.; Fang, F. [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Zhou, Y.; Sun, Y. [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Lanzhou University, Lanzhou 730000 (China); Wang, Z.M.; Sun, Y.Z. [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); University of Chinese Academy of Sciences, Beijing 100049 (China)

2017-01-21

A prototype of a new CsI(Tl) telescope, which will be used in the reaction studies of light isotopes with energy of several hundred AMeV, was constructed and tested at the Institute of Modern Physics, Chinese Academy of Sciences. The telescope has a multi-layer structure, and the range information was obtained to improve the particle identification performance. This prototype has seven layers of different thickness. An energy resolution of 5.0% (FWHM) was obtained for one of the layers in a beam test experiment. Positive improvement for the identification of {sup 14}O and {sup 15}O isotopes was achieved using the range information.

Syntheses, structural variants and characterization of AInM′S4 (A=alkali metals, Tl; M′ = Ge, Sn) compounds; facile ion-exchange reactions of layered NaInSnS4 and KInSnS4 compounds

International Nuclear Information System (INIS)

Yohannan, Jinu P.; Vidyasagar, Kanamaluru

2016-01-01

Ten AInM′S 4 (A=alkali metals, Tl; M′= Ge, Sn) compounds with diverse structure types have been synthesized and characterized by single crystal and powder X-ray diffraction and a variety of spectroscopic methods. They are wide band gap semiconductors. KInGeS 4 (1-β), RbInGeS 4 (2), CsInGeS 4 (3-β), TlInGeS 4 (4-β), RbInSnS 4 (8-β) and CsInSnS 4 (9) compounds with three-dimensional BaGa 2 S 4 structure and CsInGeS 4 (3-α) and TlInGeS 4 (4-α) compounds with a layered TlInSiS 4 structure have tetrahedral [InM′S 4 ] − frameworks. On the other hand, LiInSnS 4 (5) with spinel structure and NaInSnS 4 (6), KInSnS 4 (7), RbInSnS 4 (8-α) and TlInSnS 4 (10) compounds with layered structure have octahedral [InM′S 4 ] − frameworks. NaInSnS 4 (6) and KInSnS 4 (7) compounds undergo facile topotactic ion-exchange, at room temperature, with various mono-, di- and tri-valent cations in aqueous medium to give rise to metastable layered phases. - Graphical abstract: NaInSnS 4 and KInSnS 4 compounds undergo, in aqueous medium at room temperature, facile topotactic ion-exchange with mono, di and trivalent cations. Display Omitted - Highlights: • Ten AInM′S 4 compounds with diverse structure types were synthesized. • They are wide band gap semiconductors. • NaInSnS 4 and KInSnS 4 compounds undergo facile topotactic ion-exchange at room temperature.

Dissociation of gaseous complex fluorides MMnF3 and MMnF4 (M= Li - Cs)

International Nuclear Information System (INIS)

Sidorov, L.N.; Gubarevich, V.D.

1982-01-01

Mass spectrometric determination of dissociation enthalpies of gaseous complex fluorides CsMnF 3 and CsMnF 4 into neutral and charged particles is carried out using techniques of isothermal evaporation, electron impact and study of ion-molecular equilibria. As a result formation enthalpy values of CsMnFsub(3 gas) and CsMnFsub(4 gas) at T=298 are obtained, being -285.4 and -359.9 kcal/mol respectively

An evaluation of the subtraction photoshop software accuracy to detect minor changes in optical density by radiovisiography

Directory of Open Access Journals (Sweden)

Talaeipour AR.

2004-06-01

Full Text Available Statement of Problem: Subtraction is a newly presented radiography technique to detect minor density"nchanges that are not visible by conventional radiography."nPurpose: The aim of this In-vitro study was to evaluate the efficacy of photoshop subtraction software for"ndetecting minor density changes between two dental images."nMaterials and Methods: In this research, five dried human mandibles were held in fixed position while thin"naluminium sheets were superimposed on each mandible on the 1th and 2nd molar teeth regions."nA reference image, without aluminium sheet placement, was obtained from each mandible subsequently series"nconsist of 20 images with aluminium sheets, ranging from 50p. to "5Q0"x were recorded by radiovisiography"n(RVG system. Initial images were subtracted from subsequent ones by Photoshop subtraction software. The"ndifference in density between the two images at the 1st and 2nd molar sites was related to the aluminium"nsheets. The optical density of aluminium sheets was determined by densitometer."nResults: In the present study, 6.6% of the optical density changes of the minimum aluminium thickness as"n300u. could be detected by photoshop software software."nConclusion: The findings of this study showed that the accuracy of photoshop subtraction software was equal"nto that of the conventional subtraction softwares. Additionally, the accuracy of this software was proved to be"nsuitable for clinical investigations of small localized changes in alveolar bone.

P-T and T-x projections of phase diagram of CsF-ZrF4 system

International Nuclear Information System (INIS)

Karasev, N.M.; Korenev, Yu.M.; Sidorov, L.N.

1980-01-01

The CsF-ZrF 4 system has been investigated by the Knudsen effusion method and mass-spectral analysis of vaporization products. A molecular composition of vapour was determined. CsF, Cs 2 F 2 , ZrF 4 , Cs 2 ZrF 6 , CsZrF 5 , CsZr 2 F 9 molecules were found in the saturated vapour of the system. Heats of phase transitions and partial pressures of the molecules detected were determined depending on the melt compositions. Dissociation enthalpies of complex molecules were calculated. P-T and T-x projections of the state diagram of the CsF-ZrF 4 system were constructed

Behaviour of 137Cs in the Boreal forest ecosystem of central Sweden

International Nuclear Information System (INIS)

Fawaris, B.H.

1995-01-01

Behaviour of Chernobyl fallout 1 37 Cs in a coniferous forest ecosystem in central Sweden was investigated between 1990 and 1994. Results demonstrated that forest soil belongs to nutrient deficient type, and deposited fallout 1 37 Cs from Chernobyl nuclear accident (CNA) was retained (85%) in the upper 5 cm of humic forest soil layer, with a venial migration deeper into soil profile. No correlation between forest soil exchangeable and total potassium (K + ) and 1 37 Cs transfer parameters was observed. However, addition of K + , found to efficiently reduce 1 37 Cs uptake by sheep's fescue and the addition of stable caesium (1 33 Cs + ) enhanced it. The addition of ammonium (NH 4 + ) was slightly stimulating the uptake of 1 37 Cs by sheep's fescue in the first cut only. Field plants showed a considerably reduction in their 1 37 Cs activity concentrations. Relative to their 1 37 Cs levels of 1986-89, a little reduction in heather (16%) occurred eight years after CNA. In contrast the reductions in lingonberry and bilberry were 87% and 68%, respectively. Three fractions of forest soil bound 1 37 Cs were observed due to sequential extraction procedure (SEP). The first, is easily extractable 1 37 Cs fraction (F1+F2), it comprises 22% of total forest soil 1 37 Cs inventory in the upper 5 cm layer. The second, is soil organically and biologically bound 1 37 Cs (F3+F4) comprises about 30% of soil bound 1 37 Cs. This fraction might be accounted for long-term soil available 1 37 Cs for plant uptake after bio-degradation processes by soil microorganisms. The third, is the residual fraction (F5), it comprises more than 35% of total forest soil 1 37 Cs inventory, and may be associated with soil components which are probably of organic nature. Sorption of 1 37 Cs by zeolite (Mordenite) revealed that soil bound 1 37 Cs is to some extent more mobile in forest soils with high OM% and low pH than those with low OM%. 99 refs

Vertical profile of 137Cs in soil.

Science.gov (United States)

Krstić, D; Nikezić, D; Stevanović, N; Jelić, M

2004-12-01

In this paper, a vertical distribution of 137Cs in undisturbed soil was investigated experimentally and theoretically. Soil samples were taken from the surroundings of the city of Kragujevac in central Serbia during spring-summer of 2001. The sampling locations were chosen in such a way that the influence of soil characteristics on depth distribution of 137Cs in soil could be investigated. Activity of 137Cs in soil samples was measured using a HpGe detector and multi-channel analyzer. Based on vertical distribution of 137Cs in soil which was measured for each of 10 locations, the diffusion coefficient of 137Cs in soil was determined. In the next half-century, 137Cs will remain as the source of the exposure. Fifteen years after the Chernobyl accident, and more than 30 years after nuclear probes, the largest activity of 137Cs is still within 10 cm of the upper layer of the soil. This result confirms that the penetration of 137Cs in soil is a very slow process. Experimental results were compared with two different Green functions and no major differences were found between them. While both functions fit experimental data well in the upper layer of soil, the fitting is not so good in deeper layers. Although the curves obtained by these two functions are very close to each other, there are some differences in the values of parameters acquired by them.

Using photoshop filters to create anatomic line-art medical images.

Science.gov (United States)

Kirsch, Jacobo; Geller, Brian S

2006-08-01

There are multiple ways to obtain anatomic drawings suitable for publication or presentations. This article demonstrates how to use Photoshop to alter digital radiologic images to create line-art illustrations in a quick and easy way. We present two simple to use methods; however, not every image can adequately be transformed and personal preferences and specific changes need to be applied to each image to obtain the desired result. There are multiple ways to obtain anatomic drawings suitable for publication or to prepare presentations. Medical illustrators have always played a major role in the radiology and medical education process. Whether used to teach a complex surgical or radiologic procedure, to define typical or atypical patterns of the spread of disease, or to illustrate normal or aberrant anatomy, medical illustration significantly affects learning (). However, if you are not an accomplished illustrator, the alternatives can be expensive (contacting a professional medical illustrator or buying an already existing stock of digital images) or simply not necessarily applicable to what you are trying to communicate. The purpose of this article is to demonstrate how using Photoshop (Adobe Systems, San Jose, CA) to alter digital radiologic images we can create line-art illustrations in a quick, inexpensive, and easy way in preparation for electronic presentations and publication.

Adobe photoshop quantification (PSQ) rather than point-counting: A rapid and precise method for quantifying rock textural data and porosities

Science.gov (United States)

Zhang, Xuefeng; Liu, Bo; Wang, Jieqiong; Zhang, Zhe; Shi, Kaibo; Wu, Shuanglin

2014-08-01

Commonly used petrological quantification methods are visual estimation, counting, and image analyses. However, in this article, an Adobe Photoshop-based analyzing method (PSQ) is recommended for quantifying the rock textural data and porosities. Adobe Photoshop system provides versatile abilities in selecting an area of interest and the pixel number of a selection could be read and used to calculate its area percentage. Therefore, Adobe Photoshop could be used to rapidly quantify textural components, such as content of grains, cements, and porosities including total porosities and different genetic type porosities. This method was named as Adobe Photoshop Quantification (PSQ). The workflow of the PSQ method was introduced with the oolitic dolomite samples from the Triassic Feixianguan Formation, Northeastern Sichuan Basin, China, for example. And the method was tested by comparing with the Folk's and Shvetsov's "standard" diagrams. In both cases, there is a close agreement between the "standard" percentages and those determined by the PSQ method with really small counting errors and operator errors, small standard deviations and high confidence levels. The porosities quantified by PSQ were evaluated against those determined by the whole rock helium gas expansion method to test the specimen errors. Results have shown that the porosities quantified by the PSQ are well correlated to the porosities determined by the conventional helium gas expansion method. Generally small discrepancies (mostly ranging from -3% to 3%) are caused by microporosities which would cause systematic underestimation of 2% and/or by macroporosities causing underestimation or overestimation in different cases. Adobe Photoshop could be used to quantify rock textural components and porosities. This method has been tested to be precise and accurate. It is time saving compared with usual methods.

{sup 137}Cs in a raised bog in central Sweden

Energy Technology Data Exchange (ETDEWEB)

Rosen, K. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, Ulls vag 17, Box 7014, SE-75007, Uppsala (Sweden)], E-mail: klas.rosen@mv.slu.se; Vinichuk, M. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, Ulls vag 17, Box 7014, SE-75007, Uppsala (Sweden); Department of Ecology, Zhytomyr State Technological University, 103 Cherniakhovsky Str., 10005 Zhytomyr (Ukraine); Johanson, K.J. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, Ulls vag 17, Box 7014, SE-75007, Uppsala (Sweden)

2009-07-15

The vertical distribution of {sup 137}Cs activity in peat soil profiles and {sup 137}Cs activity concentration in plants of various species was studied in samples collected at two sites on a raised bog in central Sweden. One site (open bog) was in an area with no trees and only a few sparsely growing plant species, while the other (low pine) was less than 100 m from the open bog site and had slowly growing Scots pine, a field layer dominated by some ericaceous plants and ground well-covered by plants. The plant samples were collected in 2004-2007 and were compared with samples collected in 1989 from the same open bog and low pine sites. Ground deposition of {sup 137}Cs in 2005 was similar at both sites, 23 000 Bq m{sup -2}. In the open bog peat profile it seems to be an upward transport of caesium since a clear peak of {sup 137}Cs activity was found in the uppermost 1-4 cm of Sphagnum layers, whereas at the low pine site {sup 137}Cs was mainly found in deeper (10-12 cm) layers. The migration rate was 0.57 cm yr{sup -1} at the open bog site and the migration centre of {sup 137}Cs was at a depth of 10.7, while the rate at the low pine site was 0.78 cm yr{sup -1} and the migration centre was at 14.9 cm. Heather (Calluna vulgaris) was the plant species with the highest {sup 137}Cs activity concentrations at both sites, 43.5 k Bq{sup -1} DM in 1989 decreasing to 20.4 in 2004-2007 on open bog and 22.3 k Bq kg{sup -1} DM in 1989 decreasing to 11.2 k Bq{sup -1} DM by the period 2004-2007 on the low pine site. {sup 137}Cs transfer factors in plants varied between 0.88 and 1.35 on the open bog and between 0.48 and 0.69 m{sup 2} kg{sup -1} DM at the low pine site.

Radioactive Cs in the estuary sediments near Fukushima Daiichi Nuclear Power Plant

International Nuclear Information System (INIS)

Yamasaki, Shinya; Imoto, Junpei; Furuki, Genki; Ochiai, Asumi; Ohnuki, Toshihiko; Sueki, Keisuke; Nanba, Kenji; Ewing, Rodney C.; Utsunomiya, Satoshi

2016-01-01

The migration and dispersion of radioactive Cs (mainly "1"3"4Cs and "1"3"7Cs) are of critical concern in the area surrounding the Fukushima Daiichi Nuclear Power Plant (FDNPP). Considerable uncertainty remains in understanding the properties and dynamics of radioactive Cs transport by surface water, particularly during rainfall-induced flood events to the ocean. Physical and chemical properties of unique estuary sediments, collected from the Kuma River, 4.0 km south of the FDNPP, were quantified in this study. These were deposited after storm events and now occur as dried platy sediments on beach sand. The platy sediments exhibit median particle sizes ranging from 28 to 32 μm. There is increasing radioactivity towards the bottom of the layers deposited; approximately 28 and 38 Bq g"−"1 in the upper and lower layers, respectively. The difference in the radioactivity is attributed to a larger number of particles associated with radioactive Cs in the lower part of the section, suggesting that radioactive Cs in the suspended soils transported by surface water has decreased over time. Sequential chemical extractions showed that ~ 90% of "1"3"7Cs was strongly bound to the residual fraction in the estuary samples, whereas 60 ~ 80% of "1"3"7Cs was bound to clays in the six paddy soils. This high concentration in the residual fraction facilitates ease of transport of clay and silt size particles through the river system. Estuary sediments consist of particles < 100 μm. Radioactive Cs desorption experiments using the estuary samples in artificial seawater revealed that 3.4 ± 0.6% of "1"3"7Cs was desorbed within 8 h. More than 96% of "1"3"7Cs remained strongly bound to clays. Hence, particle size is a key factor that determines the travel time and distance during the dispersion of "1"3"7Cs in the ocean. - Highlights: • Cs-137 of estuary sediment impacted by the FDNPP was measured. • Physical and chemical properties were measured also. • Increasing radioactivity was

Pure zero-dimensional Cs4PbBr6 single crystal rhombohedral microdisks with high luminescence and stability.

Science.gov (United States)

Zhang, Haihua; Liao, Qing; Wu, Yishi; Chen, Jianwei; Gao, Qinggang; Fu, Hongbing

2017-11-08

Zero-dimensional (0D) perovskite Cs 4 PbBr 6 has been speculated to be an efficient solid-state emitter, exhibiting strong luminescense on achieving quantum confinement. Although several groups have reported strong green luminescence from Cs 4 PbBr 6 powders and nanocrystals, doubts that the origin of luminescence comes from Cs 4 PbBr 6 itself or CsPbBr 3 impurities have been a point of controversy in recent investigations. Herein, we developed a facile one-step solution self-assembly method to synthesize pure zero-dimensional rhombohedral Cs 4 PbBr 6 micro-disks (MDs) with a high PLQY of 52% ± 5% and photoluminescence full-width at half maximum (FWHM) of 16.8 nm. The obtained rhombohedral MDs were high quality single-crystalline as demonstrated by XRD and SAED patterns. We demonstrated that Cs 4 PbBr 6 MDs and CsPbBr 3 MDs were phase-separated from each other and the strong green emission comes from Cs 4 PbBr 6 . Power and temperature dependence spectra evidenced that the observed strong green luminescence of pure Cs 4 PbBr 6 MDs originated from direct exciton recombination in the isolated octahedra with a large binding energy of 303.9 meV. Significantly, isolated PbBr 6 4- octahedra separated by a Cs + ion insert in the crystal lattice is beneficial to maintaining the structural stability, depicting superior thermal and anion exchange stability. Our study provides an efficient approach to obtain high quality single-crystalline Cs 4 PbBr 6 MDs with highly efficient luminescence and stability for further optoelectronic applications.

The Photoshop Smile Design technique (part 1): digital dental photography.

Science.gov (United States)

McLaren, Edward A; Garber, David A; Figueira, Johan

2013-01-01

The proliferation of digital photography and imaging devices is enhancing clinicians' ability to visually document patients' intraoral conditions. By understanding the elements of esthetics and learning how to incorporate technology applications into clinical dentistry, clinicians can predictably plan smile design and communicate anticipated results to patients and ceramists alike. This article discusses camera, lens, and flash selection and setup, and how to execute specific types of images using the Adobe Photoshop Smile Design (PSD) technique.

Variable dimensionality and framework found in a series of quaternary zinc selenites, A{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}·xH{sub 2}O (A = Na, Rb, and Cs; 0≤x≤1) and Cs{sub 2}Zn{sub 2}(SeO{sub 3}){sub 3}·2H{sub 2}O

Energy Technology Data Exchange (ETDEWEB)

Lü, Minfeng; Jo, Hongil; Oh, Seung-Jin; Ok, Kang Min, E-mail: kmok@cau.ac.kr

2017-01-15

Five new alkali metal zinc selenites, A{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}·xH{sub 2}O (A = Na, Rb, and Cs; 0≤x≤1) and Cs{sub 2}Zn{sub 2}(SeO{sub 3}){sub 3}·2H{sub 2}O have been synthesized by heating a mixture of ZnO, SeO{sub 2} and A{sub 2}CO{sub 3} (A = Na, Rb, and Cs), and characterized by X-ray diffraction (XRD) and spectroscopic analyses techniques. All of the reported materials revealed a rich structural chemistry with different frameworks and connection modes of Zn{sup 2+}. While Rb{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4} and Cs{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}·H{sub 2}O revealed three-dimensional frameworks consisting of isolated ZnO{sub 4} tetrahedra and SeO{sub 3} polyhedra, Na{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}, Cs{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}, and Cs{sub 2}Zn{sub 2}(SeO{sub 3}){sub 3}·2H{sub 2}O contained two-dimensional [Zn{sub 3}(SeO{sub 3}){sub 4}]{sup 2-} layers. Specifically, whereas isolated ZnO{sub 4} tetrahedra and SeO{sub 3} polyhedra are arranged into two-dimensional [Zn{sub 3}(SeO{sub 3}){sub 4}]{sup 2-} layers in two cesium compounds, circular [Zn{sub 3}O{sub 10}]{sup 14-} chains and SeO{sub 3} linkers are formed in two-dimensional [Zn{sub 3}(SeO{sub 3}){sub 4}]{sup 2-} layers in Na{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}. Close structural examinations suggest that the size of alkali metal is significant in determining the framework geometry as well as connection modes of transition metal cations. - Graphical abstract: Variable dimensions and frameworks were found in a series of quaternary zinc selenites, A{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4} (A = Na, Rb and Cs). - Highlights: • Five novel quaternary zinc selenites are synthesized. • All the selenites with different structures contain polarizable d{sup 10} and lone pair cations. • The size of alkali metal cations is significant in determining the framework geometry.

The quinternary thiophosphate Cs0.5Ag0.5Nb2PS10

Directory of Open Access Journals (Sweden)

Sojeong Park

2010-07-01

Full Text Available The quinternary thiophosphate Cs0.5Ag0.5Nb2PS10, cesium silver tris(disulfido[tetrathiophosphato(V]diniobate(IV, has been prepared from the elements using a CsCl flux. The crystal structure is made up of ∞1[Nb2PS10] chains expanding along [010]. These chains are built up from bicapped trigonal-prismatic [Nb2S12] units and tetrahedral [PS4] groups and are linked through a linear S—Ag—S bridge, forming a two-dimensional layer. These layers then stack on top of each other, completing the three-dimensional structure with an undulating van der Waals gap. The disordered Cs+ ions reside on sites with half-occupation in the voids of this arrangement. Short [2.8843 (5 Å] and long [3.7316 (4 Å] Nb—Nb distances alternate along the chains, and anionic S22− and S2− species are observed. The charge balance of the compound can be represented by the formula [Cs+]0.5[Ag+]0.5[Nb4+]2[PS43−][S22−]3.

Boosting Two-Dimensional MoS2/CsPbBr3 Photodetectors via Enhanced Light Absorbance and Interfacial Carrier Separation.

Science.gov (United States)

Song, Xiufeng; Liu, Xuhai; Yu, Dejian; Huo, Chengxue; Ji, Jianping; Li, Xiaoming; Zhang, Shengli; Zou, Yousheng; Zhu, Gangyi; Wang, Yongjin; Wu, Mingzai; Xie, An; Zeng, Haibo

2018-01-24

Transition metal dichalcogenides (TMDs) are promising candidates for flexible optoelectronic devices because of their special structures and excellent properties, but the low optical absorption of the ultrathin layers greatly limits the generation of photocarriers and restricts the performance. Here, we integrate all-inorganic perovskite CsPbBr 3 nanosheets with MoS 2 atomic layers and take the advantage of the large absorption coefficient and high quantum efficiency of the perovskites, to achieve excellent performance of the TMD-based photodetectors. Significantly, the interfacial charge transfer from the CsPbBr 3 to the MoS 2 layer has been evidenced by the observed photoluminescence quenching and shortened decay time of the hybrid MoS 2 /CsPbBr 3 . Resultantly, such a hybrid MoS 2 /CsPbBr 3 photodetector exhibits a high photoresponsivity of 4.4 A/W, an external quantum efficiency of 302%, and a detectivity of 2.5 × 10 10 Jones because of the high efficient photoexcited carrier separation at the interface of MoS 2 and CsPbBr 3 . The photoresponsivity of this hybrid device presents an improvement of 3 orders of magnitude compared with that of a MoS 2 device without CsPbBr 3 . The response time of the device is also shortened from 65.2 to 0.72 ms after coupling with MoS 2 layers. The combination of the all-inorganic perovskite layer with high photon absorption and the carrier transport TMD layer may pave the way for novel high-performance optoelectronic devices.

Layered Halide Double Perovskites Cs3+nM(II)nSb2X9+3n (M = Sn, Ge) for Photovoltaic Applications.

Science.gov (United States)

Tang, Gang; Xiao, Zewen; Hosono, Hideo; Kamiya, Toshio; Fang, Daining; Hong, Jiawang

2018-01-04

Over the past few years, the development of lead-free and stable perovskite absorbers with excellent performance has attracted extensive attention. Much effort has been devoted to screening and synthesizing this type of solar cell absorbers. Here, we present a general design strategy for designing the layered halide double perovskites Cs 3+n M(II) n Sb 2 X 9+3n (M = Sn, Ge) with desired photovoltaic-relevant properties by inserting [MX 6 ] octahedral layers, based on the principles of increased electronic dimensionality. Compared to Cs 3 Sb 2 I 9 , more suitable band gaps, smaller carrier effective masses, larger dielectric constants, lower exciton binding energies, and higher optical absorption can be achieved by inserting variable [SnI 6 ] or [GeI 6 ] octahedral layers into the [Sb 2 I 9 ] bilayers. Moreover, our results show that adjusting the thickness of inserted octahedral layers is an effective approach to tune the band gaps and carrier effective masses in a large range. Our work provides useful guidance for designing the promising layered antimony halide double perovskite absorbers for photovoltaic applications.

Cs2SeO4-UO2SeO4-H2O system at 25 deg C

International Nuclear Information System (INIS)

Serezhkina, L.B.; Serezhkin, V.N.

1987-01-01

Using the method of isothermal solubility at 25 deg C the interaction of cesium and uranyl selenates in aqueous solution is studied. Formation of congruently soluble Cs 2 UO 2 (SeO 4 ) 2 x2H 2 O and Cs 2 (UO 2 ) 2 x(SeO 4 ) 3 is ascertained, their crystallographic characteristics being determined

Conductivity And Thermal Stability of Solid Acid Composites CsH2PO4 /NaH2PO4/ SiO2

International Nuclear Information System (INIS)

Norsyahida Mohammad; Abu Bakar Mohamad; Abu Bakar Mohamad; Abdul Amir Hassan Kadhum

2016-01-01

Solid acid composites CsH 2 PO 4 / NaH 2 PO 4 / SiO 2 with different mole ratios of CsH 2 PO 4 and NaH 2 PO 4 to SiO 2 were synthesized and characterized. Preliminary infrared measurements of CsH 2 PO 4 and its composites indicated that hydrogen bonds breaking and formation were detected between 1710 to 2710 cm -1 , while the rotation of phosphate tetrahedral anions occurred between 900 and 1200 cm -1 . The superprotonic transition of CsH 2 PO 4 / NaH 2 PO 4 / SiO 2 composite was identified at superprotonic temperatures between 230 and 260 degree Celcius, under atmospheric pressure. This study reveals higher conductivity values for composites with higher CsH 2 PO 4 (CDP) content. Solid acid composite CDP 613 appeared as the composite with the highest conductivity that is 7.2x10 -3 S cm -1 at 230 degree Celcius. Thermal stability of the solid acid composites such as temperature of dehydration, melting and decomposition were investigated. The addition of NaH 2 PO 4 lowers the dehydration temperature of the solid acid composites. (author)

Development of the CsI Calorimeter Subsystem for AMEGO

Science.gov (United States)

Grove, J. Eric; Woolf, Richard; Johnson, W. Neil; Phlips, Bernard

2018-01-01

We report on the development of the thallium-doped cesium iodide (CsI:Tl) calorimeter subsystem for the All-Sky Medium-Energy Gamma-ray Observatory (AMEGO). The CsI calorimeter is one of the three main subsystems that comprise the AMEGO instrument suite; the others include the double-sided silicon strip detector (DSSD) tracker/converter and a cadmium zinc telluride (CZT) calorimeter. Similar to the LAT instrument on Fermi, the hodoscopic calorimeter consists of orthogonally layered CsI bars. Unlike the LAT, which uses PIN photodiodes, the scintillation light readout from each end of the CsI bar is done with recently developed large-area silicon photomultiplier (SiPM) arrays. We currently have an APRA program to develop the calorimeter technology for a larger, future space-based gamma-ray observatory. Under this program, we are building and testing a prototype calorimeter consisting of 24 CsI bars (16.7 mm x 16.7 mm x 100 mm) arranged in 4 layers with 6 bars per layer. The ends of each bar are read out with a 2 x 2 array of 6 mm x 6 mm SensL J series SiPMs. Signal readout and processing is done with the IDEAS SIPHRA (IDE3380) ASIC. Performance testing of this prototype will be done with laboratory sources, a beam test, and a balloon flight in conjunction with the other subsystems led by NASA GSFC. Additionally, we will test 16.7 mm x 16.7 mm x 450 mm CsI bars with SiPM readout to understand the performance of longer bars in advance of the developing the full instrument.Acknowledgement: This work was sponsored by the Chief of Naval Research (CNR) and NASA-APRA (NNH15ZDA001N-APRA).

Magnetic biodegradable Fe3O4/CS/PVA nanofibrous membranes for bone regeneration

International Nuclear Information System (INIS)

Wei Yan; Zhang Xuehui; Hu Xiaoyang; Deng Xuliang; Song Yu; Lin Yuanhua; Han Bing; Wang Xinzhi

2011-01-01

In recent years, interest in magnetic biomimetic scaffolds for tissue engineering has increased considerably. The aim of this study is to develop magnetic biodegradable fibrous materials with potential use in bone regeneration. Magnetic biodegradable Fe 3 O 4 /chitosan (CS)/poly vinyl alcohol (PVA) nanofibrous membranes were achieved by electrospinning with average fiber diameters ranging from 230 to 380 nm and porosity of 83.9-85.1%. The influences of polymer concentration, applied voltage and Fe 3 O 4 nanoparticles loading on the fabrication of nanofibers were investigated. The polymer concentration of 4.5 wt%, applied voltage of 20 kV and Fe 3 O 4 nanoparticles loading of lower than 5 wt% could produce homogeneous, smooth and continuous Fe 3 O 4 /CS/PVA nanofibrous membranes. X-ray diffraction (XRD) data confirmed that the crystalline structure of the Fe 3 O 4 , CS and PVA were maintained during electrospinning process. Fourier transform infrared spectroscopy (FT-IR) demonstrated that the Fe 3 O 4 loading up to 5 wt% did not change the functional groups of CS/PVA greatly. Transmission electron microscopy (TEM) showed islets of Fe 3 O 4 nanoparticles evenly distributed in the fibers. Weak ferrimagnetic behaviors of membranes were revealed by vibrating sample magnetometer (VSM) test. Tensile test exhibited Young's modulus of membranes that were gradually enhanced with the increase of Fe 3 O 4 nanoparticles loading, while ultimate tensile stress and ultimate strain were slightly reduced by Fe 3 O 4 nanoparticles loading of 5%. Additionally, MG63 human osteoblast-like cells were seeded on the magnetic nanofibrous membranes to evaluate their bone biocompatibility. Cell growth dynamics according to MTT assay and scanning electron microscopy (SEM) observation exhibited good cell adhesion and proliferation, suggesting that this magnetic biodegradable Fe 3 O 4 /CS/PVA nanofibrous membranes can be one of promising biomaterials for facilitation of osteogenesis.

Volatility of components of saturated vapours of UCl/sub 4/-CsCl and UCl/sub 4/-LiCl molten mixtures

Energy Technology Data Exchange (ETDEWEB)

Smirnov, M V; Kudyakov, V Ya; Salyulev, A B; Komarov, V E; Posokhin, Yu V; Afonichkin, V K

1979-01-01

The flow method has been used for measuring the volatility of the components from UCl/sub 4/-CsCl and UCl/sub 4/-LiCl melted mixtures containing 2.0, 5.0, 12.0, 25.0, 33.0, 50.0, 67.0, and 83.0 mol.% of UCl/sub 4/ within the temperature ranges of 903-1188 K and 740-1200 K, respectively. The chemical composition of saturated vapours above the melted salts has been determined. The melted mixtures in question exhibit negative deviation from ideal behaviour. Made was the conclusion about the presence in a vapour phase, along with monomeric UCl/sub 4/, LiCl, CsCl and Li/sub 2/Cl/sub 2/, Cs/sub 2/Cl/sub 2/ dimers of double compounds of the MeUCl/sub 5/ most probable composition. Their absolute contribution into a total pressure above the UCl/sub 4/-CsCl melted mixtures is considerably smaller than above the UCl/sub 4/ -LiCl mixtures.

Chemical interaction between (Cs-Te) doped fuels and cladding material under irradiation

International Nuclear Information System (INIS)

Delbrassine, A.; Flipot, A.J.

1977-01-01

Pins containing UO 2 -30 wt.% PuO 2 low density pellets and or caesium and or tellurium as doping elements have been irradiated for about 40 days in the BR 2 reactor. The effect of two Cs/Te ratios, namely 1.3 and 4, and a wide range of O/M ratios on the inner corrosion of the clad has been investigated. The influence of tellurium on the attack of the cladding has been pointed out. It may be responsible for the chromium and nickel depletion in the grain boundaries of the steal. The corrosion patterns and the thickness of the corroded layer could be different in the total length of a fuel pin. It seems therefore necessary to measure the effective Cs/Te ratio associated with the local corrosion layers. This local Cs/Te ratio should be more useful than the initial mean Cs/Te ratio in a pin for understanding the corrosion phenomena. (author)

Hydrothermal synthesis and crystal structure of CsFe23(HPO4)2(PO4)(H2O)

International Nuclear Information System (INIS)

Anisimova, N.Yu.; Ilyukhin, A.B.; Chudinova, N.N.; Serafin, M.

2001-01-01

The double acid iron-cesium orthophosphate CsFe 2 3 (HPO 4 ) 2 (PO 4 )(H 2 O) was prepared by hydrothermal synthesis (from the Fe 2 O 3 , Cs 2 CO 3 and H 3 PO 4 mixture at 290 Deg C during 1 h following by cooling to 25 Deg C). Its crystal structure (a = 5.021(3), b = 15.80(1), c = 13.646(8), β 94.49(4) Deg, sp. gr. P2 1 /n, Z = 4) was analyzed by X-ray diffraction. The structure is formed by the orthophosphate tetrahedrons and the FeO 6 octahedrons, the water molecule is coordinated by the iron atom [ru

Single-crystal X-ray diffraction study of Cs{sub 2}Er[Si{sub 6}O{sub 14}]F and Cs{sub 2}Er[Si{sub 4}O{sub 10}]F

Energy Technology Data Exchange (ETDEWEB)

Dabic, Predrag; Kremenovic, Aleksandar; Vulic, Predag [Belgrade Univ. (Serbia). Lab. of Crystallography; Kahlenberg, Volker; Schmidmair, Daniela [Innsbruck Univ. (Austria). Inst. of Mineralogy and Petrography

2016-07-01

Single-crystal growth experiments in the system CsF-Er{sub 2}O{sub 3}-SiO{sub 2} resulted in the simultaneous crystallization of two chemically related compounds within the same run: Cs{sub 2}Er[Si{sub 6}O{sub 14}]F (phase I) and Cs{sub 2}Er[Si{sub 4}O{sub 10}]F (phase II). They represent the first examples for cesium erbium silicates containing fluorine. Basic crystallographic data are - phase I: space group Cmca, a=17.2556(6) Aa, b=24.6565(7) Aa, c=14.4735(5) Aa, V=6157.9(3) Aa{sup 3}, Z=16; phase II: space group Pnma, a=22.3748(7) Aa, b=8.8390(2) Aa, c=11.9710(4) Aa, V=2367.5(1) Aa{sup 3}, Z=8. The structures were determined by direct methods and refined to residuals of R(vertical stroke F vertical stroke)=0.0229 for 2920 (phase I) and 0.0231 for 2314 (phase II) independent observed reflections with I>2σ(I). The structure of phase I represents a previously unknown structure type with a three dimensional tetrahedral framework consisting of Q{sup 3} and Q{sup 4} groups in the ratio 2:1. Basic building units of the network are unbranched sechser single-chains running parallel to [001]. The network can be conveniently built up from the condensation of tetrahedral layers parallel to (010) or (100), respectively. The crystal structure of phase II can be classified as a tubular or columnar chain silicate indicating that the backbones of the structure are multiple chains of silicate tetrahedra. This structure is isotypic to a Cs{sub 2}Y[Si{sub 4}O{sub 10}]F, a compound that has been characterized previously. Alternatively, both compounds can be described as mixed octahedral-tetrahedral frameworks, which can be classified according to their polyhedral microensembles. A topological analysis of both nets is presented.

Contrast enhancement of bite mark images using the grayscale mixer in ACR in Photoshop®.

Science.gov (United States)

Evans, Sam; Noorbhai, Suzanne; Lawson, Zoe; Stacey-Jones, Seren; Carabott, Romina

2013-05-01

Enhanced images may improve bite mark edge definition, assisting forensic analysis. Current contrast enhancement involves color extraction, viewing layered images by channel. A novel technique, producing a single enhanced image using the grayscale mix panel within Adobe Camera Raw®, has been developed and assessed here, allowing adjustments of multiple color channels simultaneously. Stage 1 measured RGB values in 72 versions of a color chart image; eight sliders in Photoshop® were adjusted at 25% intervals, all corresponding colors affected. Stage 2 used a bite mark image, and found only red, orange, and yellow sliders had discernable effects. Stage 3 assessed modality preference between color, grayscale, and enhanced images; on average, the 22 survey participants chose the enhanced image as better defined for nine out of 10 bite marks. The study has shown potential benefits for this new technique. However, further research is needed before use in the analysis of bite marks. © 2013 American Academy of Forensic Sciences.

Ion conductivities of ZrF4-BaF2-CsF glasses

International Nuclear Information System (INIS)

Kawamoto, Yoji; Nohara, Ichiro

1987-01-01

The glass-forming region in the ZrF 4 -BaF 2 -CsF glass system has been determined and the ac conductivity and the transport number of fluoride ions have been measured. The conductivities of compounds β-Cs 2 ZrF 6 , α-SrZrF 6 , α-BaZrF 6 , β-BaZrF 6 and α-PbZrF 6 have also been measured. These results and a previous study of ZrF 4 -BaF 2 -MF n (M: the groups I-IV metals) glasses revealed the following: (1) the ZrF 4 -BaF 2 -CsF glasses are exclusively fluoride-ion conductors; (2) the ionic conductivities of ZrF 4 -based glasses are predominantly determined by the activation energies for conduction; (3) the activation energy for conduction decreases with an increase in the average polarizability of glass-constituting cations; (4) a decrease in average Zr-F bond length and a lowering of the average F coordination number of Zr are presumed to increase the activation energy for conduction. Principles of developing ZrF 4 -based glasses with higher conductivities have also been proposed. (Auth.)

Low-temperature liquid-phase epitaxy and optical waveguiding of rare-earth-ion-doped KY(WO4)2 thin layers

NARCIS (Netherlands)

Romanyuk, Y.E.; Utke, I.; Ehrentraut, D.; Apostolopoulos, V.; Pollnau, Markus; Garcia-Revilla, S.; Valiente, B.

2004-01-01

Crystalline $KY(WO_{4})_{2}$ thin layers doped with different rare-earth ions were grown on b-oriented, undoped $KY(WO_{4})_{2}$ substrates by liquid-phase epitaxy employing a low-temperature flux. The ternary chloride mixture of NaCl, KCl, and CsCl with a melting point of 480°C was used as a

Integrating multi-omics analyses of Nonomuraea dietziae to reveal the role of soybean oil in [(4'-OH)MeLeu]4-CsA overproduction.

Science.gov (United States)

Liu, Huanhuan; Huang, Di; Jin, Lina; Wang, Cheng; Liang, Shaoxiong; Wen, Jianping

2017-07-14

Nonomuraea dietziae is a promising microorganism to mediate the region-specific monooxygenation reaction of cyclosporine A (CsA). The main product [(4'-OH)MeLeu] 4 -CsA possesses high anti-HIV/HCV and hair growth-stimulating activities while avoiding the immunosuppressive effect of CsA. However, the low conversion efficiency restricts the clinical application. In this study, the production of [(4'-OH)MeLeu] 4 -CsA was greatly improved by 55.6% from 182.8 to 284.4 mg/L when supplementing soybean oil into the production medium, which represented the highest production of [(4'-OH)MeLeu] 4 -CsA so far. To investigate the effect of soybean oil on CsA conversion, some other plant oils (corn oil and peanut oil) and the major hydrolysates of soybean oil were fed into the production medium, respectively. The results demonstrated that the plant oils, rather than the hydrolysates, could significantly improve the [(4'-OH)MeLeu] 4 -CsA production, suggesting that soybean oil might not play its role in the lipid metabolic pathway. To further unveil the mechanism of [(4'-OH)MeLeu] 4 -CsA overproduction under the soybean oil condition, a proteomic analysis based on the two-dimensional gel electrophoresis coupled with MALDI TOF/TOF mass spectrometry was implemented. The results showed that central carbon metabolism, genetic information processing and energy metabolism were significantly up-regulated under the soybean oil condition. Moreover, the gas chromatography-mass spectrometry-based metabolomic analysis indicated that soybean oil had a great effect on amino acid metabolism and tricarboxylic acid cycle. In addition, the transcription levels of cytochrome P450 hydroxylase (CYP) genes for CsA conversion were determined by RT-qPCR and the results showed that most of the CYP genes were up-regulated under the soybean oil condition. These findings indicate that soybean oil could strengthen the primary metabolism and the CYP system to enhance the mycelium growth and the

Zero-Dimensional Cs4PbBr6 Perovskite Nanocrystals

KAUST Repository

Zhang, Yuhai; Saidaminov, Makhsud I.; Dursun, Ibrahim; Yang, Haoze; Banavoth, Murali; Alarousu, Erkki; Yengel, Emre; Alshankiti, Buthainah; Bakr, Osman; Mohammed, Omar F.

2017-01-01

class of materials remains elusive. Here we report the synthesis of a new class of colloidal semiconductor NCs based on Cs4PbBr6, the 0-D perovskite, enabled through the design of a novel low-temperature reverse microemulsion method with 85% reaction

Evaluation of a new electronic preoperative reference marker for toric intraocular lens implantation by two different methods of analysis: Adobe Photoshop versus iTrace.

Science.gov (United States)

Farooqui, Javed Hussain; Sharma, Mansi; Koul, Archana; Dutta, Ranjan; Shroff, Noshir Minoo

2017-01-01

The aim of this study is to compare two different methods of analysis of preoperative reference marking for toric intraocular lens (IOL) after marking with an electronic marker. Cataract and IOL Implantation Service, Shroff Eye Centre, New Delhi, India. Fifty-two eyes of thirty patients planned for toric IOL implantation were included in the study. All patients had preoperative marking performed with an electronic preoperative two-step toric IOL reference marker (ASICO AE-2929). Reference marks were placed at 3-and 9-o'clock positions. Marks were analyzed with two systems. First, slit-lamp photographs taken and analyzed using Adobe Photoshop (version 7.0). Second, Tracey iTrace Visual Function Analyzer (version 5.1.1) was used for capturing corneal topograph examination and position of marks noted. Amount of alignment error was calculated. Mean absolute rotation error was 2.38 ± 1.78° by Photoshop and 2.87 ± 2.03° by iTrace which was not statistically significant ( P = 0.215). Nearly 72.7% of eyes by Photoshop and 61.4% by iTrace had rotation error ≤3° ( P = 0.359); and 90.9% of eyes by Photoshop and 81.8% by iTrace had rotation error ≤5° ( P = 0.344). No significant difference in absolute amount of rotation between eyes when analyzed by either method. Difference in reference mark positions when analyzed by two systems suggests the presence of varying cyclotorsion at different points of time. Both analysis methods showed an approximately 3° of alignment error, which could contribute to 10% loss of astigmatic correction of toric IOL. This can be further compounded by intra-operative marking errors and final placement of IOL in the bag.

Radioactive Cs in the estuary sediments near Fukushima Daiichi Nuclear Power Plant

Energy Technology Data Exchange (ETDEWEB)

Yamasaki, Shinya, E-mail: s-yamasaki@ied.tsukuba.ac.jp [Faculty of Pure and Applied Sciences and Center for Research in Isotopes and Environmental Dynamics, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577 (Japan); Imoto, Junpei; Furuki, Genki; Ochiai, Asumi [Department of Chemistry, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan); Ohnuki, Toshihiko [Advanced Science Research Center, Japan Atomic Energy Agency, Shirakata Shirane 2-4, Tokai, Ibaraki 319-1195 (Japan); Sueki, Keisuke [Faculty of Pure and Applied Sciences and Center for Research in Isotopes and Environmental Dynamics, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577 (Japan); Nanba, Kenji [Department of Environmental Management, Faculty of Symbiotic System Science, Fukushima University, Kanayagawa 1, Fukushima, 960-1296 (Japan); Ewing, Rodney C. [Department of Geological Sciences and Center for International Security and Cooperation, Stanford University, Stanford, CA 94305-2115 (United States); Utsunomiya, Satoshi [Department of Chemistry, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan)

2016-05-01

The migration and dispersion of radioactive Cs (mainly {sup 134}Cs and {sup 137}Cs) are of critical concern in the area surrounding the Fukushima Daiichi Nuclear Power Plant (FDNPP). Considerable uncertainty remains in understanding the properties and dynamics of radioactive Cs transport by surface water, particularly during rainfall-induced flood events to the ocean. Physical and chemical properties of unique estuary sediments, collected from the Kuma River, 4.0 km south of the FDNPP, were quantified in this study. These were deposited after storm events and now occur as dried platy sediments on beach sand. The platy sediments exhibit median particle sizes ranging from 28 to 32 μm. There is increasing radioactivity towards the bottom of the layers deposited; approximately 28 and 38 Bq g{sup −1} in the upper and lower layers, respectively. The difference in the radioactivity is attributed to a larger number of particles associated with radioactive Cs in the lower part of the section, suggesting that radioactive Cs in the suspended soils transported by surface water has decreased over time. Sequential chemical extractions showed that ~ 90% of {sup 137}Cs was strongly bound to the residual fraction in the estuary samples, whereas 60 ~ 80% of {sup 137}Cs was bound to clays in the six paddy soils. This high concentration in the residual fraction facilitates ease of transport of clay and silt size particles through the river system. Estuary sediments consist of particles < 100 μm. Radioactive Cs desorption experiments using the estuary samples in artificial seawater revealed that 3.4 ± 0.6% of {sup 137}Cs was desorbed within 8 h. More than 96% of {sup 137}Cs remained strongly bound to clays. Hence, particle size is a key factor that determines the travel time and distance during the dispersion of {sup 137}Cs in the ocean. - Highlights: • Cs-137 of estuary sediment impacted by the FDNPP was measured. • Physical and chemical properties were measured also. �

Molecular structures and thermodynamic properties of 12 gaseous cesium-containing species of nuclear safety interest: Cs 2, CsH, CsO, Cs 2O, CsX, and Cs 2X 2 (X = OH, Cl, Br, and I)

Science.gov (United States)

Badawi, Michael; Xerri, Bertrand; Canneaux, Sébastien; Cantrel, Laurent; Louis, Florent

2012-01-01

Ab initio electronic structure calculations at the coupled cluster level with a correction for the triples extrapolated to the complete basis set limit have been made for the estimation of the thermochemical properties of Cs 2, CsH, CsO, Cs 2O, CsX, and Cs 2X 2 (X = OH, Cl, Br, and I). The standard enthalpies of formation and standard molar entropies at 298 K, and the temperature dependence of the heat capacities at constant pressure were evaluated. The calculated thermochemical properties are in good agreement with their literature counterparts. For Cs 2, CsH, CsOH, Cs 2(OH) 2, CsCl, Cs 2Cl 2, CsBr, CsI, and Cs 2I 2, the calculated ΔfH298K∘ values are within chemical accuracy of the most recent experimental values. Based on the excellent agreement observed between our calculated ΔfH298K∘ values and their literature counterparts, the standard enthalpies of formation at 298 K are estimated to be the following: ΔfH298K∘ (CsO) = 17.0 kJ mol -1 and ΔfH298K∘ (Cs 2Br 2) = -575.4 kJ mol -1.

Syntheses, structural variants and characterization of AInM′S{sub 4} (A=alkali metals, Tl; M′ = Ge, Sn) compounds; facile ion-exchange reactions of layered NaInSnS{sub 4} and KInSnS{sub 4} compounds

Energy Technology Data Exchange (ETDEWEB)

Yohannan, Jinu P.; Vidyasagar, Kanamaluru, E-mail: kvsagar@iitm.ac.in

2016-06-15

Ten AInM′S{sub 4} (A=alkali metals, Tl; M′= Ge, Sn) compounds with diverse structure types have been synthesized and characterized by single crystal and powder X-ray diffraction and a variety of spectroscopic methods. They are wide band gap semiconductors. KInGeS{sub 4}(1-β), RbInGeS{sub 4}(2), CsInGeS{sub 4}(3-β), TlInGeS{sub 4}(4-β), RbInSnS{sub 4}(8-β) and CsInSnS{sub 4}(9) compounds with three-dimensional BaGa{sub 2}S{sub 4} structure and CsInGeS{sub 4}(3-α) and TlInGeS{sub 4}(4-α) compounds with a layered TlInSiS{sub 4} structure have tetrahedral [InM′S{sub 4}]{sup −} frameworks. On the other hand, LiInSnS{sub 4}(5) with spinel structure and NaInSnS{sub 4}(6), KInSnS{sub 4}(7), RbInSnS{sub 4}(8-α) and TlInSnS{sub 4}(10) compounds with layered structure have octahedral [InM′S{sub 4}]{sup −} frameworks. NaInSnS{sub 4}(6) and KInSnS{sub 4}(7) compounds undergo facile topotactic ion-exchange, at room temperature, with various mono-, di- and tri-valent cations in aqueous medium to give rise to metastable layered phases. - Graphical abstract: NaInSnS{sub 4} and KInSnS{sub 4} compounds undergo, in aqueous medium at room temperature, facile topotactic ion-exchange with mono, di and trivalent cations. Display Omitted - Highlights: • Ten AInM′S{sub 4} compounds with diverse structure types were synthesized. • They are wide band gap semiconductors. • NaInSnS{sub 4} and KInSnS{sub 4} compounds undergo facile topotactic ion-exchange at room temperature.

Anti-fouling and high water permeable forward osmosis membrane fabricated via layer by layer assembly of chitosan/graphene oxide

Science.gov (United States)

Salehi, Hasan; Rastgar, Masoud; Shakeri, Alireza

2017-08-01

To date, forward osmosis (FO) has received considerable attention due to its potential application in seawater desalination. FO does not require external hydraulic pressure and consequently is believed to have a low fouling propensity. Despite the numerous privileges of FO process, a major challenge ahead for its development is the lack of high performance membranes. In this study, we fabricated a novel highly-efficient FO membrane using layer-by-layer (LbL) assembly of positive chitosan (CS) and negative graphene oxide (GO) nanosheets via electrostatic interaction on a porous support layer. The support layer was prepared by blending hydrophilic sulfonated polyethersulfone (SPES) into polyethersulfone (PES) matrix using wet phase inversion process. Various characterization techniques were used to confirm successful fabrication of LbL membrane. The number of layers formed on the SPES-PES support layer was easily adjusted by repeating the CS and GO deposition cycles. Thin film composite (TFC) membrane was also prepared by the same SPES-PES support layer and polyamide (PA) active layer to compare membranes performances. The water permeability and salt rejection of the fabricated membranes were obtained by two kinds of draw solutions (including Na2SO4 and sucrose) under two different membrane orientations. The results showed that membrane coated by a CS/GO bilayers had water flux of 2-4 orders of magnitude higher than the TFC one. By increasing the number of CS/GO bilayers, the selectivity of the LbL membrane was improved. The novel fabricated LbL membrane showed better fouling resistance than the TFC one in the feed solution containing 200 ppm of sodium alginate as a foulant model.

Ammonothermal synthesis and characterization of Cs{sub 2}[Zn(NH{sub 2}){sub 4}

Energy Technology Data Exchange (ETDEWEB)

Richter, Theresia M.M.; Niewa, Rainer [Institut fuer Anorganische Chemie, Universitaet Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart (Germany); Alt, Nicolas S.A.; Schluecker, Eberhard [Lehrstuhl fuer Prozessmaschinen und Anlagentechnik, Friedrich-Alexander-Universitaet Erlangen-Nuernberg, Cauerstrasse 4, 91058, Erlangen (Germany)

2016-10-15

Cs{sub 2}[Zn(NH{sub 2}){sub 4}] was synthesized under ammonothermal conditions (sc-NH{sub 3}, 523 K, 155 MPa) from CsNH{sub 2} and Zn. Growth of cm-sized crystals succeeded upon application of a temperature gradient. The crystal structure is based on the motif of a hexagonal closed packing of [Zn(NH{sub 2}){sub 4}]{sup 2-} ions with occurrence of no significant hydrogen bridges according to distances and vibrational spectroscopy. Cs{sup +} ions are located within octahedral and tetrahedral holes of the packing. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

The feature and distribution of 137Cs in the forest soil

International Nuclear Information System (INIS)

Narazaki, Yukinori

2002-01-01

The 137 Cs concentration in an undisturbed upper layer of naked land in Fukuoka Prefecture decreased exponentially from 1969 to 1999 with the apparent half-life of 7 years. The ratio of 137 Cs concentration in the lower layer of the soil to that in the upper layer was about 1/5. The concentration of 137 Cs, 40 K, and stable Cs and the soil profile consisting of loss on ignition, pH, and electric conductivity were determined in the 48 samples collected in the forests and the neighboring naked land from 1991 to 1998. The 137 Cs concentration in the forest soils ranged from 1 to 424 Bq/kg dry wt, 131 Bq/kg dry wt on average, although 137 Cs was hardly detected in the naked soil around the forest. There was no regional difference in the distribution of the 137 Cs concentration, and it varied with pH and electric conductivity in the soil. Further, it tended to be higher in the deciduous woodland than in the evergreen woodland. (author)

Regeneration of Used Frying Palm Oil with Coffee Silverskin (CS), CS Ash (CSA) and Nanoparticles of CS (NCS).

Science.gov (United States)

Ismail, Samir Abd-Elmonem A; El-Anany, Ayman Mohammed; Ali, Rehab Farouk M

2017-01-01

The present investigation aimed to evaluate the efficiency of coffee silverskin (CS), CS ash (CSA) and nanoparticles of CS (NCS) in regeneration the quality of used frying palm oil. The adsorbents were mixed individually with used frying palm oil at level 4% (w/v) for 60 min. The properties of CS, CSA and NCS adsorbents were studied using (SEM) scanning electron microscopy technique. Some of physico-chemical characteristics of used frying palm oil (UFPO) and UFPO treated with adsorbents were determined. The results showed that the CS ash particles composed of irregular spherical and semispherical grains with deep cavities. The size of particles of CS ash ranged in diameter from 1.1 to 1.7 µm. The morphology of NCS consisted of cluster-type spherical nanoparticles and flakes. The particle size of NCS varies from 0.9 to 1.7 µm. Purification treatments caused marked (poil compared to untreated oil. The treatment of UFPO with 4% of adsorbents caused significant reductions in the content of free fatty acids ranged from 51.2 to 65.0%. The lowest level of peroxide (2.1 meq/kg) was recorded for UFPO treated with 4% of NCS. The highest reductions (72.8; 70.0%) in p-anisidine value were observed in UFPO treated with 4% of CSA and NCS, respectively. Treatment of UFPO with 4% of CS, CSA and NCS significantly lowered the polar content from 13.9% to 6.3, 4.8 and 3.9%, respectively. The results also indicate that CSA and NCS have nearly the same adsorption efficiency in lowering polymer content of UFPO. Filtration treatment of UFPO with 4% of CS, CSA and NCS markedly lowered the viscosity and colour values of treated UFPO.

Foundation Flash CS4 for Designers

CERN Document Server

Green, Tom

2008-01-01

In this book, you'll learn:* How to create effective animations using the new Motion Editor and animation tools * How to use the new 3D features to animate objects in 3D space * Best-practice tips and techniques from some of the top Flash practitioners on the planet * How to create captioned video and full-screen video, and deploy HD video using Flash * Techniques for using the Flash UI components as well as XML documents to create stunning,interactive presentations If you're a Flash designer looking for a solid overview of Flash CS4, this book is for you. Through the use of solid and practica

Isolation and sequence analysis of pCS36-4CPA, a small plasmid from Citrobacter sp. 36-4CPA.

Science.gov (United States)

Zharikova, Natalia V; Iasakov, Timur R; Bumazhkin, Boris K; Patutina, Ekaterina O; Zhurenko, Evgeniia I; Korobov, Vladislav V; Sagitova, Alina I; Kuznetsov, Boris B; Markusheva, Tatiana V

2018-05-01

A small plasmid designated pCS36-4CPA with a size of 5217 base pairs and G-C content of 50.74% was isolated from Citrobacter sp. 36-4CPA. The origin of replication ( ori ) of the plasmid was identified as a region of about 800 bp in length with an identity of 67.1% to the ColE1 plasmid at the nucleotide level. The replication region contained typical elements of ColE1-like plasmids: RNA I and RNA II with their corresponding -10 and -35 boxes, a single-strand initiation site ( ssi ), and a lagging-strand termination site ( terH ). As seen in other ColE1-like plasmids, pCS36-4CPA carried mobilisation machinery that include mobABCD genes but it did not possess the rom gene. Analysis of the multimer resolution site ( mrs ) was performed and XerC and XerD binding sites were identified. Also, the 70-nt transcript Rcd of pCS36-4CPA was predicted and similarity of the transcript's secondary structure with those of the ColE1-family was shown. The cargo module of pCS36-4CPA contained three open reading frames (ORFs). Two of them (ORF5 and ORF6) showed no significant homology to any known gene sequences but contained putative THAP DNA-binding (DBD) and type II restriction endonuclease Eco O109I domains. The seventh open reading frame (ORF7) encodes YhdJ-like DNA modification methylase. The region highly homologous to pCS36-4CPA was found in the Salmonella phage SE2 genome.

Evaluation of photoshop based image analysis in cytologic diagnosis of pleural fluid in comparison with conventional modalities.

Science.gov (United States)

Jafarian, Amir Hossein; Tasbandi, Aida; Mohamadian Roshan, Nema

2018-04-19

The aim of this study is to investigate and compare the results of digital image analysis in pleural effusion cytology samples with conventional modalities. In this cross-sectional study, 53 pleural fluid cytology smears from Qaem hospital pathology department, located in Mashhad, Iran were investigated. Prior to digital analysis, all specimens were evaluated by two pathologists and categorized into three groups as: benign, suspicious, and malignant. Using an Olympus microscope and Olympus DP3 digital camera, digital images from cytology slides were captured. Appropriate images (n = 130) were separately imported to Adobe Photoshop CS5 and parameters including area and perimeter, circularity, Gray Value mean, integrated density, and nucleus to cytoplasm area ratio were analyzed. Gray Value mean, nucleus to cytoplasm area ratio, and circularity showed the best sensitivity and specificity rates as well as significant differences between all groups. Also, nucleus area and perimeter showed a significant relation between suspicious and malignant groups with benign group. Whereas, there was no such difference between suspicious and malignant groups. We concluded that digital image analysis is welcomed in the field of research on pleural fluid smears as it can provide quantitative data to apply various comparisons and reduce interobserver variation which could assist pathologists to achieve a more accurate diagnosis. © 2018 Wiley Periodicals, Inc.

[The concentration and distribution of 137Cs in soils of forest and agricultural ecosystems of Tula Region].

Science.gov (United States)

Lipatov, D N; Shcheglov, A I; Tsvetnova, O B

2007-01-01

The paper deals with a comparative study of 137Cs contamination in forest, old arable and cultivated soils of Tula Region. Initial interception of Chernobyl derived 137Cs is higher in forest ecosystems: oak-forest > birch-forest > pine-forest > agricultural ecosystems. Vertical migration of 137Cs in deeper layers of soils was intensive in agricultural ecosystems: cultivated soils > old arable soils > birch-forest soils > oak-forest soils > pine-forest soils. In study have been evaluated spatial variability of 137Cs in soil and asymmetrical distribution, that is a skew to the right. Spatial heterogeneity of 137Cs in agricultural soils is much lower than in forest soils. For cultivated soil are determined the rate of resuspension, which equal to 6.1 x 10(-4) day(-1). For forest soils are described the 137Cs concentration in litter of different ecosystems. The role of main accumulation and barrier of 137Cs retain higher layers of soils (horizon A1(A1E) in forest, horizon Ap in agricultural ecosystems) in long-term forecast after Chernobyl accident.

Electronic structure and optical properties of Cs2HgI4: Experimental study and band-structure DFT calculations

Science.gov (United States)

Lavrentyev, A. A.; Gabrelian, B. V.; Vu, V. T.; Shkumat, P. N.; Myronchuk, G. L.; Khvyshchun, M.; Fedorchuk, A. O.; Parasyuk, O. V.; Khyzhun, O. Y.

2015-04-01

High-quality single crystal of cesium mercury tetraiodide, Cs2HgI4, has been synthesized by the vertical Bridgman-Stockbarger method and its crystal structure has been refined. In addition, electronic structure and optical properties of Cs2HgI4 have been studied. For the crystal under study, X-ray photoelectron core-level and valence-band spectra for pristine and Ar+-ion irradiated surfaces have been measured. The present X-ray photoelectron spectroscopy (XPS) results indicate that the Cs2HgI4 single crystal surface is very sensitive with respect to Ar+ ion-irradiation. In particular, Ar+ bombardment of the single crystal surface alters the elemental stoichiometry of the Cs2HgI4 surface. To elucidate peculiarities of the energy distribution of the electronic states within the valence-band and conduction-band regions of the Cs2HgI4 compound, we have performed first-principles band-structure calculations based on density functional theory (DFT) as incorporated in the WIEN2k package. Total and partial densities of states for Cs2HgI4 have been calculated. The DFT calculations reveal that the I p states make the major contributions in the upper portion of the valence band, while the Hg d, Cs p and I s states are the dominant contributors in its lower portion. Temperature dependence of the light absorption coefficient and specific electrical conductivity has been explored for Cs2HgI4 in the temperature range of 77-300 K. Main optical characteristics of the Cs2HgI4 compound have been elucidated by the first-principles calculations.

Intrinsic Lead Ion Emissions in Zero-Dimensional Cs4PbBr6 Nanocrystals

KAUST Repository

Yin, Jun

2017-11-07

We investigate the intrinsic lead ion (Pb2+) emissions in zero-dimensional (0D) perovskite nanocrystals (NCs) using a combination of experimental and theoretical approaches. The temperature-dependent photoluminescence experiments for both “nonemissive” (highly suppressed green emission) and emissive (bright green emission) Cs4PbBr6 NCs show a splitting of emission spectra into high- and low-energy transitions in the ultraviolet (UV) spectral range. In the nonemissive case, we attribute the high-energy UV emission at approximately 350 nm to the allowed optical transition of 3P1 to 1S0 in Pb2+ ions and the low-energy UV emission at approximately 400 nm to the charge-transfer state involved in the 0D NC host lattice (D-state). In the emissive Cs4PbBr6 NCs, in addition to the broad UV emission, we demonstrate that energy transfer occurs from Pb2+ ions to green luminescent centers. The optical phonon modes in Cs4PbBr6 NCs can be assigned to both Pb–Br stretching and rocking motions from density functional theory calculations. Our results address the origin of the dual broadband Pb2+ ion emissions observed in Cs4PbBr6 NCs and provide insights into the mechanism of ionic exciton–optical phonon interactions in these 0D perovskites.

High-temperature behavior of dicesium molybdate Cs{sub 2}MoO{sub 4}: Implications for fast neutron reactors

Energy Technology Data Exchange (ETDEWEB)

Wallez, Gilles, E-mail: gilles.wallez@upmc.fr [Institut de Recherche de Chimie Paris, CNRS—Chimie ParisTech, 11 rue Pierre et Marie Curie, 75005 Paris (France); Université Pierre et Marie Curie, 4 place Jussieu, 75005 Paris (France); Raison, Philippe E., E-mail: philippe.raison@ec.europa.eu [European Commission, Joint Research Centre, Institute for Transuranium Elements, 76125 Karlsruhe (Germany); Smith, Anna L., E-mail: anna.smith@ec.europa.eu [European Commission, Joint Research Centre, Institute for Transuranium Elements, 76125 Karlsruhe (Germany); Department of Materials Science and Metallurgy, University of Cambridge, 27 Charles Babbage Road, Cambridge CB3 0FS (United Kingdom); Clavier, Nicolas, E-mail: nicolas.clavier@cea.fr [ICSM–UMR5257 CNRS/CEA/UM2/ENSCM, Site de Marcoule, Bât 426, BP 17171, 30207 Bagnols/Cèze (France); Dacheux, Nicolas, E-mail: nicolas.dacheux@cea.fr [ICSM–UMR5257 CNRS/CEA/UM2/ENSCM, Site de Marcoule, Bât 426, BP 17171, 30207 Bagnols/Cèze (France)

2014-07-01

Dicesium molybdate (Cs{sub 2}MoO{sub 4})'s thermal expansion and crystal structure have been investigated herein by high temperature X ray diffraction in conjunction with Raman spectroscopy. This first crystal-chemical insight at high temperature is aimed at predicting the thermostructural and thermomechanical behavior of this oxide formed by the accumulation of Cs and Mo fission products at the periphery of nuclear fuel rods in sodium-cooled fast reactors. Within the temperature range of the fuel's rim, Cs{sub 2}MoO{sub 4} becomes hexagonal P6{sub 3}/mmc, with disordered MoO{sub 4} tetrahedra and 2D distribution of Cs–O bonds that makes thermal axial expansion both large (50≤α{sub l}≤70 10{sup −6} °C{sup −1}, 500–800 °C) and highly anisotropic (α{sub c}−α{sub a}=67×10{sup −6} °C{sup −1}, hexagonal form). The difference with the fuel's expansion coefficient is of potential concern with respect to the cohesion of the Cs{sub 2}MoO{sub 4} surface film and the possible release of cesium radionuclides in accidental situations. - Graphical abstract: The weakness of the Cs–O bonds and the disordering of the MoO{sub 4} tetrahedra array in the high-temperature form are responsible for the huge thermal expansion of Cs{sub 2}MoO{sub 4} along the c-axis. - Highlights: • Thermomechanical behavior of Cs{sub 2}MoO{sub 4} fission products compound is studied. • High-temperature form of Cs{sub 2}MoO{sub 4} is characterized by XRD and Raman. • Thermal expansion appears very high and anisotropic. • Cohesion between Cs{sub 2}MoO{sub 4} and nuclear fuel seems questionable, and Cs release is expected.

Accumulation and translocation peculiarities of "1"3"7Cs and "4"0K in the soil – plant system

International Nuclear Information System (INIS)

Marčiulionienė, Danutė; Lukšienė, Benedikta; Jefanova, Olga

2015-01-01

Long-term investigations (1996–2008) were conducted into the "1"3"7Cs and "4"0K in the soil of forests, swamps and meadows in different regions of Lithuania, as well as in the plants growing in these media. The "1"3"7Cs and "4"0K activity concentrations, the "1"3"7Cs/"4"0K activity concentration ratio and accumulation, and translocation in the system, i.e. from the soil to plant roots to above-ground plant part of these radionuclides, were evaluated after gamma-spectrometric measurements using a high purity germanium (HPGe) detector. Based on the obtained data, it can be asserted that in the tested plant species, the "1"3"7Cs and "4"0K accumulation, the transfer from soil to roots and translocation within the plants depend on the plant species and environmental ecological conditions. The "1"3"7Cs/"4"0K activity concentration ratios in the same plant species in different regions of Lithuania are different and this ratio depends on the biotope (forest, swamp or meadow) in which the plant grows and on the location of the growing region. Based on the determined trends of statistically reliable inverse dependence between the activity concentrations in both soil and plants, it can be stated that the exchange of "1"3"7Cs and "4"0K in plants and soil is different. Different accumulations and translocations of investigated radionuclides in the same plant species indicate diverse biological metabolism of "1"3"7Cs and its chemical analogue "4"0K in plants. A competitive relationship exists between "1"3"7Cs and "4"0K in plants as well as in the soil. - Highlights: • Investigations of "1"3"7Cs and "4"0K were performed in different ecological conditions. • The data indicate a diverse biological metabolism of "1"3"7Cs and "4"0K in plant species. • A pronounced association between "1"3"7Cs and "4"0K in soil and plants is not statistically significant. • A competitive relationship exists between "1"3"7Cs and "4"0K in plants as well as in the soil. • The ratio of "1

Fractionation of (137)Cs and Pu in natural peatland.

Science.gov (United States)

Mihalík, Ján; Bartusková, Miluše; Hölgye, Zoltán; Ježková, Tereza; Henych, Ondřej

2014-08-01

High Cs-137 concentrations in plants growing on peatland inspired us to investigate the quantity of its bioavailable fraction in natural peat. Our investigation aims to: a) estimate the quantity of bioavailable Cs-137 and Pu present in peat, b) verify the similarity of Cs-137 and K-40 behaviours, and c) perform a quantification of Cs-137 and Pu transfer from peat to plants. We analysed the vertical distribution of Cs-137 and Pu isotopes in the peat and their concentrations in plants growing on these places. Bioavailability of radionuclides was investigated by sequential extraction. Sequential analyses revealed that it was the upper layer which contained the majority of Cs-137 in an available form while deeper layers retained Cs-137 in immobile fractions. We can conclude that 18% of all Cs-137 in the peat is still bioavailable. Despite of the low quantity of bioavailable fraction of Cs-137 its transfer factor reached extremely high values. In the case of Pu, 64% of its total amount was associated with fulvic/humic acids which resulted in the high transfer factor from peat to plants. 27 years after the Chernobyl nuclear accident, the significant part of radionuclides deposited in peatland is still bioavailable. Copyright © 2014 Elsevier Ltd. All rights reserved.

Fractionation of 137Cs and Pu in natural peatland

International Nuclear Information System (INIS)

Mihalík, Ján; Bartusková, Miluše; Hölgye, Zoltán; Ježková, Tereza; Henych, Ondřej

2014-01-01

High Cs-137 concentrations in plants growing on peatland inspired us to investigate the quantity of its bioavailable fraction in natural peat. Our investigation aims to: a) estimate the quantity of bioavailable Cs-137 and Pu present in peat, b) verify the similarity of Cs-137 and K-40 behaviours, and c) perform a quantification of Cs-137 and Pu transfer from peat to plants. We analysed the vertical distribution of Cs-137 and Pu isotopes in the peat and their concentrations in plants growing on these places. Bioavailability of radionuclides was investigated by sequential extraction. Sequential analyses revealed that it was the upper layer which contained the majority of Cs-137 in an available form while deeper layers retained Cs-137 in immobile fractions. We can conclude that 18% of all Cs-137 in the peat is still bioavailable. Despite of the low quantity of bioavailable fraction of Cs-137 its transfer factor reached extremely high values. In the case of Pu, 64% of its total amount was associated with fulvic/humic acids which resulted in the high transfer factor from peat to plants. 27 years after the Chernobyl nuclear accident, the significant part of radionuclides deposited in peatland is still bioavailable. - Highlights: • Decrease of exchangeable 137 Cs and its increase in residual fraction with depth. • High 137 Cs transfer factor contrary to its low quantity in bioavailable fractions. • Fulvic/humic acids are a more effective carrier for Pu than for Cs

[Distribution of 137Cs and relative influencing factors on typical karst sloping land].

Science.gov (United States)

Zhang, Xiao-Nan; Wang, Ke-Lin; Zhang, Wei; Chen, Hong-Song; He, Xun-Yang; Zhang, Xin-Bao

2009-11-01

Based on the field survey and the analysis of a large number of soil samples, the distribution of 137 Cs and its influencing factors were studied using 137 Cs tracer technology on typical karst sloping land. The results indicate that the distribution of 137 Cs in soil profile in karst areas show the similar characteristics as that in non-karst areas, fitted an exponential pattern in forest soils and a uniform pattern in cultivated soils. In the sinkhole points in karst areas, 137 Cs exists in deep soil layers and its specific activity vary from 1.7 to 3.3 Bq/kg in soil layers above 45cm, suggesting the existing soil around karst sinkhole is mainly formed by the accumulation of erosion materials. The 137 Cs specific activity in the soil from two rock cracks are 16.8 Bq/kg and 37.6 Bq/kg respectively, which are much higher than that in the soil around the rock, this phenomenon indicates that bare rock is an important influencing factor for 137 Cs spatial movement. With the increment of altitude, the 137 Cs area activity exhibits an irregular fluctuation and evident spatial heterogeneity. On the forest land, the 137 Cs area activities which range from 299.4 to 1 592.6 Bq/m2 are highly positively correlated with the slope gradient and positively correlated with the altitude; while on the cultivated land, the 137 Cs area activities which range from 115.8 to 1478.6 Bq/m2 are negatively correlated with the slope gradient but negatively correlated with the altitude. Topography, geomorphology and human disturbance intensity are the key factors influencing 137 Cs spatial distribution.

The high temperature synthesis of CsAlSiO 4-ANA, a new polymorph in the system Cs 2OAl 2O 3SiO 2. I. The end member of ANA type of zeolite framework

Science.gov (United States)

Dimitrijevic, R.; Dondur, V.; Petranovic, N.

1991-12-01

High temperature phase transformations of Cs + exchanged zeolites were investigated. Above 1000°C, CsX, CsY (FAU), and Cs, ZK-4 (LTA) frameworks recrystallized in a pollucite phase. A Cs + loaded mordenite recrystallized at 1300°C in the orthorhombic CsAlSi 5O 12 phase. A Cs + exchanged zeolite A at 960°C recrystallized in a mixture of two polymorphic CsAlSiO 4 phases having different (Al,Si)O 4 frameworks. The unstable orthorhombic CsAlSiO 4ABW phase has a topotactic transition at 1150°C into an ordered low CsAlSiO 4-ANA framework. Further calcination produces, at 1200°C, transformation of the low CsAlSiO 4-ANA phase to the more stable high CsAlSiO 4-ANA polymorph having cubic ( a 0 = 13.6595 (5) Å) symmetry and an ordered SiAl distribution. The crystal structure of high CsAlSiO 4ANA, a new polymorph in the system Cs 2OAl 2O 3SiO 2, was determined using X-ray Rietveld analyses and 29Si MAS NMR spectroscopy.

137Cs in northern Adriatic sediments

International Nuclear Information System (INIS)

Barisic, D.; Lulic, S.; Vdovic, N.; Vertacnik, A.; Juracic, M.

1996-01-01

The activity of 137 Cs in shallow northern Adriatic sediments was obtained on the basis of measurement results from 25 sediment box cores, sampled during the Adriatic Scientific COoperation Program (ASCOP) 16 cruise in the summer 1990. 137 Cs was determined in surface sediments (0-3 cm) and 12-15 cm-deep sediment. It was found that the lowest caesium concentrations correspond to sands, which are spread along the Croatian coast. Parallel to the Italian coast, 137 Cs concentrations in pelites are the highest. It seems that the influence of Po River is significant for 137 Cs activities in recent marine sediments along Italian coast south of Po River delta. Significantly higher 137 Cs activities in 0-3 cm sediment layer can be attributed to the deposition caused by Chernobyl accident. (author)

The first quinary rare earth thiophosphates. Cs{sub 5}Ln{sub 3}X{sub 3}(P{sub 2}S{sub 6}){sub 2}(PS{sub 4}) (Ln = La, Ce, X = Br, Cl) and the quasi-quaternary Cs{sub 10}Y{sub 4}Cl{sub 10}(P{sub 2}S{sub 6}){sub 3}

Energy Technology Data Exchange (ETDEWEB)

Schoop, Leslie Mareike; Eger, Roland; Nuss, Juergen; Pielnhofer, Florian [Max Planck Institute for Solid State Research, Stuttgart (Germany); Lotsch, Bettina Valeska [Max Planck Institute for Solid State Research, Stuttgart (Germany); Nanosystems Initiative Munich (NIM) and Center for Nanoscience, Muenchen (Germany)

2017-12-13

We report the first examples of quinary rare earth thiophosphates with a fully ordered cation and anion distribution, Cs{sub 5}Ln{sub 3}X{sub 3}(P{sub 2}S{sub 6}){sub 2}(PS{sub 4}), (Ln = La, Ce and X = Br, Cl) as well as the quasi-quaternary Cs{sub 10}Y{sub 4}Cl{sub 10}(P{sub 2}S{sub 6}){sub 3}. These four new compounds crystallize in three different, unknown structure types. The yellowish, transparent, brittle Cs{sub 5}Ce{sub 3}Br{sub 3}(P{sub 2}S{sub 6}){sub 2}(PS{sub 4}) crystallizes in the orthorhombic space group Pnma (no. 62) with a = 13.276(3), b = 14.891(3), c = 19.593(4) Aa, and V = 3873(1) Aa{sup 3} in a novel structure type. Colorless crystals of Cs{sub 5}La{sub 3}Br{sub 3}(P{sub 2}S{sub 6}){sub 2}(PS{sub 4}) and Cs{sub 5}La{sub 3}Cl{sub 3}(P{sub 2}S{sub 6}){sub 2}(PS{sub 4}) are isotypic and were obtained in the monoclinic space group P2{sub 1}/m (no. 11) with a = 9.715(2), b = 14.310(3), c = 13.685(3) Aa, β = 100.16(3) and V = 1873(1) Aa{sup 3} and a = 9.513(2), b = 14.182(3), c = 13.699(3) Aa, β = 99.39(3) and V = 1823(1) Aa{sup 3}, respectively. Both structures contain isolated hexathiohypodiphosphate(IV) [P{sub 2}S{sub 6}]{sup 4-} and thiophosphate [PS{sub 4}]{sup 3-} units that are arranged alternately in layers. Cs{sub 10}Y{sub 4}Cl{sub 10}(P{sub 2}S{sub 6}){sub 3} crystallizes in colorless transparent platelets in the orthorhombic space group Pnnm (no. 58) with a = 13.153(3), b = 28.964(6), c = 7.780(2) Aa, and V = 2964(1) Aa{sup 3}. The structure is composed of isolated [P{sub 4/2}S{sub 6}]{sup 4-} octahedra containing four half occupied P positions surrounded octahedrally by sulfur. We show with Raman scattering that this disordered thiophosphate anion shows a Raman spectrum that is distinct from spectra published for other literature-known thiophosphate anions. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Enhanced quantum efficiency for CsI grown on a graphite-based substrate coating

CERN Document Server

Friese, J; Homolka, J; Kastenmüller, A; Maier-Komor, P; Peter, M; Zeitelhack, K; Kienle, P; Körner, H J

1999-01-01

Quantum efficiencies (QE) in the vacuum ultraviolet (VUV) wavelength region have been measured for solid CsI layers on various substrates. The CsI films were deposited applying electron beam evaporation. The QE measurements were performed utilizing synchrotron radiation as well as light from a deuterium lamp. A GaAsP diode with a sensitivity calibration traceable to a primary radiation standard was used for normalization. For CsI layers grown on resin-stabilized graphite films a significant enhancement of QE was observed. Substrates suitable for gas detector applications and aging properties were investigated. The procedures to prepare and reproduce high quantum efficient CsI layers are described.

Cs/CsPbX3 (X = Br, Cl) epitaxial heteronanocrystals with magic-angle stable/metastable grain boundary

Science.gov (United States)

Zhang, Yumeng; Fan, Baolu; Wu, Wenhui; Fan, Jiyang

2017-05-01

Metal-semiconductor heteronanostructures are crucial building blocks of nanoscale electronic and optoelectronic devices. However, the lattice misfit remains a challenge in constructing heteronanostructures. Perovskite nanocrystals are superior candidates for constructing nanodevices owing to excellent optical, ferroelectric, and superconducting properties. We report the epitaxial growth of lattice-matched Cs/CsPbBr3 metal-semiconductor heteronanocrystals in a liquid medium. The well-crystallized ultrathin Cs layers grow epitaxially on the surfaces of colloidal CsPbBr3 nanocrystals, forming heteronanocrystals with interface diameters of several nanometers. Most of them are pseudomorphic with coherent interfaces free from dislocations, and the others exhibit discrete high-angle grain boundaries. The model based on the calculation of the elastic potential energy of the epilayer and analysis of the near-coincidence sites explains well the experimental result. The analysis shows that the excellent lattice match between the metal and the semiconductor ensures the ideal epitaxial-growth of both Cs/CsPbBr3 and Cs/CsPbCl3 heteronanocrystals. Such metal/semiconductor heteronanocrystals pave the way for developing perovskite-based nanodevices.

Changes in content and synthesis of collagen types and proteoglycans in osteoarthritis of the knee joint and comparison of quantitative analysis with Photoshop-based image analysis.

Science.gov (United States)

Lahm, Andreas; Mrosek, Eike; Spank, Heiko; Erggelet, Christoph; Kasch, Richard; Esser, Jan; Merk, Harry

2010-04-01

The different cartilage layers vary in synthesis of proteoglycan and of the distinct types of collagen with the predominant collagen Type II with its associated collagens, e.g. types IX and XI, produced by normal chondrocytes. It was demonstrated that proteoglycan decreases in degenerative tissue and a switch from collagen type II to type I occurs. The aim of this study was to evaluate the correlation of real-time (RT)-PCR and Photoshop-based image analysis in detecting such lesions and find new aspects about their distribution. We performed immunohistochemistry and histology with cartilage tissue samples from 20 patients suffering from osteoarthritis compared with 20 healthy biopsies. Furthermore, we quantified our results on the gene expression of collagen type I and II and aggrecan with the help of real-time (RT)-PCR. Proteoglycan content was measured colorimetrically. Using Adobe Photoshop the digitized images of histology and immunohistochemistry stains of collagen type I and II were stored on an external data storage device. The area occupied by any specific colour range can be specified and compared in a relative manner directly from the histogram using the "magic wand tool" in the select similar menu. In the image grow menu gray levels or luminosity (colour) of all pixels within the selected area, including mean, median and standard deviation, etc. are depicted. Statistical Analysis was performed using the t test. With the help of immunohistochemistry, RT-PCR and quantitative RT- PCR we found that not only collagen type II, but also collagen type I is synthesized by the cells of the diseased cartilage tissue, shown by increasing amounts of collagen type I mRNA especially in the later stages of osteoarthritis. A decrease of collagen type II is visible especially in the upper fibrillated area of the advanced osteoarthritic samples, which leads to an overall decrease. Analysis of proteoglycan showed a loss of the overall content and a quite uniform staining in

Asian Rhinoplasty: Preoperative Simulation and Planning Using Adobe Photoshop.

Science.gov (United States)

Kiranantawat, Kidakorn; Nguyen, Anh H

2015-11-01

A rhinoplasty in Asians differs from a rhinoplasty performed in patients of other ethnicities. Surgeons should understand the concept of Asian beauty, the nasal anatomy of Asians, and common problems encountered while operating on the Asian nose. With this understanding, surgeons can set appropriate goals, choose proper operative procedures, and provide an outcome that satisfies patients. In this article the authors define the concept of an Asian rhinoplasty-a paradigm shift from the traditional on-top augmentation rhinoplasty to a structurally integrated augmentation rhinoplasty-and provide a step-by-step procedure for the use of Adobe Photoshop as a preoperative program to simulate the expected surgical outcome for patients and to develop a preoperative plan for surgeons.

Modeling radionuclide Cs and C dynamics in an artificial forest ecosystem in Japan -FoRothCs ver1.0-

Directory of Open Access Journals (Sweden)

Kazuya eNishina

2015-09-01

Full Text Available Predicting the environmental fate of Cs radionuclides in forest ecosystems is important for the effective management and assessment of radioactively contaminated forest areas. A large proportion of the radioactively contaminated areas in Japan consist of forest ecosystems, and most of these areas are artificial forests that are used for timber production (e.g., Japanese cedar (Cryptomeria japonica and red pine (Pinus densiflora. Determining the long-term redistribution of 137Cs in forest ecosystems is important for estimating human doses and understanding the ecological impacts and challenges associated with managing contaminated forests. To facilitate the management and 137Cs decontamination of these forests, we developed a new open-source 137Cs cycling model, ForRothCs, that considers C cycling within forests, as well as biomass production and soil decomposition processes. For the 137Cs inventory, this model estimates the dynamics (Bq m−2 and activity (Bq kg−2 of 137Cs on a decadal time scale, primarily in the leaves, branches, stems, litter layer, and the soil. This model is based on the biomass production and the dynamics of the C cycle models. We tested the model by considering a simple scenario of forest management, i.e., thinning and harvesting, for the first five years following a fallout event. The results showed that these activities have a limited impact on the 137Cs inventory due to the rapid migration of 137Cs from vegetation to soil. Our projections also showed the examined forest management practices resulted in reduced litterfall, which in turn reduced C input to the forest floor and increased the concentration of 137Cs in the litterfall and soil organic layer. Although further validation of the ForRothCs model is required using field observation data, the model can be used to evaluate long-term 137Cs dynamics associated with commonly used forest and decontamination management scenarios.

A Technique Using Calibrated Photography and Photoshop for Accurate Shade Analysis and Communication.

Science.gov (United States)

McLaren, Edward A; Figueira, Johan; Goldstein, Ronald E

2017-02-01

This article reviews the critical aspects of controlling the shade-taking environment and discusses various modalities introduced throughout the years to acquire and communicate shade information. Demonstrating a highly calibrated digital photographic technique for capturing shade information, this article shows how to use Photoshop® to standardize images and extract color information from the tooth and shade tab for use by a ceramist for an accurate shade-matching restoration.

Selective Se-for-S substitution in Cs-bearing uranyl compounds

Energy Technology Data Exchange (ETDEWEB)

Gurzhiy, Vladislav V., E-mail: vladgeo17@mail.ru [Department of Crystallography, St. Petersburg State University, University Emb. 7/9, 199034 St. Petersburg, Russia Federation (Russian Federation); Tyumentseva, Olga S.; Krivovichev, Sergey V. [Department of Crystallography, St. Petersburg State University, University Emb. 7/9, 199034 St. Petersburg, Russia Federation (Russian Federation); Tananaev, Ivan G. [Far Eastern Federal University, Suhanova st. 8, Vladivostok 690950 (Russian Federation)

2017-04-15

Phase formation in the mixed sulfate-selenate aqueous system of uranyl nitrate and cesium nitrate has been investigated. Two types of crystalline compounds have been obtained and characterized using a number of experimental (single crystal XRD, FTIR, SEM) and theoretical (information-based complexity calculations, topological analysis) techniques. No miscibility gaps have been observed for Cs{sub 2}[(UO{sub 2}){sub 2}(TO{sub 4}){sub 3}] (T= S, Se), which crystallizes in tetragonal system, P-42{sub 1}m, a =9.616(1)–9.856(2), c =8.105(1)–8.159(1) Å, V =749.6(2)–792.5(3) Å{sup 3}. Nine phases with variable amount of S and Se have been structurally characterized. The structures of the Cs{sub 2}[(UO{sub 2}){sub 2}(TO{sub 4}){sub 3}] (T= S, Se) compounds are based upon the [(UO{sub 2}){sub 2}(TO{sub 4}){sub 3}]{sup 2-} layers of corner-sharing uranyl pentagonal bipyramids and TO{sub 4} tetrahedra. The layers contain two types of tetrahedral sites: T1 (3-connected, i.e. having three O atoms shared by adjacent uranyl polyhedra) and T2 (4-connected). The Se-for-S substitution in tetrahedral sites is highly selective with smaller S{sup 6+} cation showing a strong preference for the more tightly bonded T2 site. Crystallization in the pure Se system starts with the formation of Cs{sub 2}[(UO{sub 2})(SeO{sub 4}){sub 2}(H{sub 2}O)](H{sub 2}O) crystals, its subsequent dissolution and formation of Cs{sub 2}[(UO{sub 2}){sub 2}(SeO{sub 4}){sub 3}]. The information-based structural complexity calculations for these two phases support the rule that more topologically complex structures form at the latest stages of crystallization. - Graphical abstract: Nine phases representing the Cs{sub 2}[(UO{sub 2}){sub 2}(TO{sub 4}){sub 3}] (T= S, Se) solid solution series with variable amount of S and Se have been prepared by isothermal evaporation from aqueous solutions and characterized using a number of experimental and theoretical techniques. No immiscibility is observed between the

Low temperature phase transition and crystal structure of CsMgPO{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Orlova, Maria, E-mail: maria.p.orlova@gmail.com [Institute of Mineralogy and Petrography, University of Innsbruck, Innrain 52, Innsbruck 6020 (Austria); Khainakov, Sergey [Departamento de Química Física y Analítica, Universidad de Oviedo—CINN, 33006 Oviedo (Spain); Servicios Científico Técnicos, Universidad de Oviedo, 33006 Oviedo (Spain); Michailov, Dmitriy [Department of Chemistry, University of Nizhny Novgorod, 23 Gagarin av., Nizhny Novgorod 603950 (Russian Federation); Perfler, Lukas [Institute of Mineralogy and Petrography, University of Innsbruck, Innrain 52, Innsbruck 6020 (Austria); Langes, Christoph [Institute of Pharmacy, University of Innsbruck, Innrain 52, Innsbruck 6020 (Austria); Kahlenberg, Volker [Institute of Mineralogy and Petrography, University of Innsbruck, Innrain 52, Innsbruck 6020 (Austria); Orlova, Albina [Department of Chemistry, University of Nizhny Novgorod, 23 Gagarin av., Nizhny Novgorod 603950 (Russian Federation)

2015-01-15

CsMgPO{sub 4} doped with radioisotopes is a promising compound for usage as a radioactive medical source. However, a low temperature phase transition at temperatures close to ambient conditions (∼−40 °C) was observed. Information about such kind of structural changes is important in order to understand whether it can cause any problem for medical use of this compound. The phase transition has been investigated in detail using synchrotron powder diffraction, Raman spectroscopy and DFT calculations. The structure undergoes a transformation from an orthorhombic modification, space group Pnma (RT phase) to a monoclinic polymorph, space group P2{sub 1}/n (LT phase). New LT modification adopts similar to RT but slightly distorted unit cell: a=9.58199(2) Å, b=8.95501(1) Å, c=5.50344(2) Å, β=90.68583(1)°, V=472.198(3) Å{sup 3}. CsMgPO{sub 4} belongs to the group of framework compounds and is made up of strictly alternating MgO{sub 4}- and PO{sub 4}-tetrahedra sharing vertices. The cesium counter cations are located in the resulting channel-like cavities. Upon the transformation a combined tilting of the tetrahedra is observed. A comparison with other phase transitions in ABW-type framework compounds is given. - Graphical abstract: Structural behavior of β-tridymite-type phosphate CsMgPO{sub 4}, considered as potential chemical form for radioactive Cs-source has been studied at near ambient temperatures. A phase transition at (∼−40 °C) has been found and investigated. It has been established that the known orthorhombic RT modification, space group Pnma, adopts a monoclinic cell with space group P2{sub 1}/n at low temperatures. In this paper, we present results of structural analysis of changes accompanying this phase transition and discuss its possible impact on the application properties. - Highlights: • β-Tridymite type phosphate CsMgPO{sub 4} undergoes so called translationengleiche phase transition of index 2 at −40 °C. • The structure

Residual contamination from Cs-137 in the Sondrio area (Lombardy - Italy)

International Nuclear Information System (INIS)

Rimoldi, E.M.; Leonardi, L.; Cavallone, E.; Bignazzi, R.; Galimberti, A.

2000-01-01

The authors conducted the investigations on the contamination by Cs-137, resulting from Chernobyl's Accident, in the Sondrio area (Lombardy, Italy). Analyses were performed with NaI (T1) spectrometer. 130 samples collected from superficial earth layer (up to 15 cm) and deep earth layer (from 15 to 30 cm) of woods and meadows, pond's mud, mosses, mushrooms, wild wood fruits, forages, striated muscle from deer, chamois and roe deer, goat's and cow's milk, and running and stagnant water, were studied. Superficial earth samples always showed a higher Cs-137 concentration compared to deep earth samples, their mean activities being 68 Bq/kg (sup. wood) and 18 Bq/kg (sup. meadow). In 1 sample from superficial wood earth in Val Belsivo, the concentration was 1109 Bq/kg. The mud samples had a mean Cs-137 concentration of 96 Bq/kg. Cs-137 was always present in mosses with a mean activity of 234 Bq/kg, whereas in mushrooms contamination was continuous (mean, 63 Bq/kg). Cs-137 was absent in wild wood fruits and in forages except for one sample of bilberry (12 Bq/Kg) and one sample of forage (54 Bq/Kg). In the striated muscle samples from wild animals, chamois always showed high Cs-137 concentration (29 Bq/kg), but was intermediate in roe deer (18 Bq/kg) and lowest in deer (5 Bq/kg). In 4 deer and 4 roe deer, contamination was undetectable. Running and stagnant waters, and cow's milk were not contaminated whereas some Cs-137 activities were detected in goat milk samples (18 Bq/kg). It is concluded that residual contamination from Chernobyl's accident in the investigated areas has by now just become a scientific interest and no longer a sanitary issue, as the contamination levels detected in all the samples are clearly below the maximal admissible levels established by the European Gazettes. However, it is interesting to note that the recycling of Cs-137 is more present in wood, confirming the delicate environmental balance of this ecosystem. The routine radio

Magnetic biodegradable Fe{sub 3}O{sub 4}/CS/PVA nanofibrous membranes for bone regeneration

Energy Technology Data Exchange (ETDEWEB)

Wei Yan; Zhang Xuehui; Hu Xiaoyang; Deng Xuliang [Department of Geriatric Dentistry, School and Hospital of Stomatology, Peking University, Beijing, 100081 (China); Song Yu; Lin Yuanhua [State Key Laboratory of New Ceramics and Fine Processing, Department of Materials Science and Engineering, Tsinghua University, Beijing, 100084 (China); Han Bing [Department of Orthodontics, School and Hospital of Stomatology, Peking University, Beijing, 100081 (China); Wang Xinzhi, E-mail: kqdengxuliang@bjmu.edu.cn [Department of Prosthodontics, School and Hospital of Stomatology, Peking University, Beijing, 100081 (China)

2011-10-15

In recent years, interest in magnetic biomimetic scaffolds for tissue engineering has increased considerably. The aim of this study is to develop magnetic biodegradable fibrous materials with potential use in bone regeneration. Magnetic biodegradable Fe{sub 3}O{sub 4}/chitosan (CS)/poly vinyl alcohol (PVA) nanofibrous membranes were achieved by electrospinning with average fiber diameters ranging from 230 to 380 nm and porosity of 83.9-85.1%. The influences of polymer concentration, applied voltage and Fe{sub 3}O{sub 4} nanoparticles loading on the fabrication of nanofibers were investigated. The polymer concentration of 4.5 wt%, applied voltage of 20 kV and Fe{sub 3}O{sub 4} nanoparticles loading of lower than 5 wt% could produce homogeneous, smooth and continuous Fe{sub 3}O{sub 4}/CS/PVA nanofibrous membranes. X-ray diffraction (XRD) data confirmed that the crystalline structure of the Fe{sub 3}O{sub 4}, CS and PVA were maintained during electrospinning process. Fourier transform infrared spectroscopy (FT-IR) demonstrated that the Fe{sub 3}O{sub 4} loading up to 5 wt% did not change the functional groups of CS/PVA greatly. Transmission electron microscopy (TEM) showed islets of Fe{sub 3}O{sub 4} nanoparticles evenly distributed in the fibers. Weak ferrimagnetic behaviors of membranes were revealed by vibrating sample magnetometer (VSM) test. Tensile test exhibited Young's modulus of membranes that were gradually enhanced with the increase of Fe{sub 3}O{sub 4} nanoparticles loading, while ultimate tensile stress and ultimate strain were slightly reduced by Fe{sub 3}O{sub 4} nanoparticles loading of 5%. Additionally, MG63 human osteoblast-like cells were seeded on the magnetic nanofibrous membranes to evaluate their bone biocompatibility. Cell growth dynamics according to MTT assay and scanning electron microscopy (SEM) observation exhibited good cell adhesion and proliferation, suggesting that this magnetic biodegradable Fe{sub 3}O{sub 4}/CS/PVA nanofibrous

Behaviour of {sup 137}Cs in the Boreal forest ecosystem of central Sweden

Energy Technology Data Exchange (ETDEWEB)

Fawaris, B.H.

1995-12-31

Behaviour of Chernobyl fallout 1{sup 37}Cs in a coniferous forest ecosystem in central Sweden was investigated between 1990 and 1994. Results demonstrated that forest soil belongs to nutrient deficient type, and deposited fallout 1{sup 37}Cs from Chernobyl nuclear accident (CNA) was retained in the upper 5 cm of humic forest soil layer, with a venial migration deeper into soil profile. No correlation between forest soil exchangeable and total potassium (K{sup +}) and 1{sup 37}Cs transfer parameters was observed. However, addition of K{sup +}, found to efficiently reduce 1{sup 37}Cs uptake by sheep`s fescue and the addition of stable caesium (1{sup 33}Cs{sup +}) enhanced it. The addition of ammonium (NH{sub 4}{sup +}) was slightly stimulating the uptake of 1{sup 37}Cs by sheep`s fescue in the first cut only. Field plants showed a considerably reduction in their 1{sup 37}Cs activity concentrations. Relative to their 1{sup 37}Cs levels of 1986-89, a little reduction in heather occurred eight years after CNA. In contrast the reductions in lingonberry and bilberry were 87% and 68%, respectively. Three fractions of forest soil bound 1{sup 37}Cs were observed due to sequential extraction procedure (SEP). The first, is easily extractable 1{sup 37}Cs fraction, it comprises 22% of total forest soil 1{sup 37}Cs inventory in the upper 5 cm layer. The second, is soil organically and biologically bound 1{sup 37}Cs comprises about 30% of soil bound 1{sup 37}Cs. This fraction might be accounted for long-term soil available 1{sup 37}Cs for plant uptake after bio-degradation processes by soil microorganisms. The third, is the residual fraction, it comprises more than 35% of total forest soil 1{sup 37}Cs inventory, and may be associated with soil components which are probably of organic nature. Sorption of 1{sup 37}Cs by zeolite (Mordenite) revealed that soil bound 1{sup 37}Cs is to some extent more mobile in forest soils with high OM% and low pH than those with low OM%.

Behaviour of {sup 137}Cs in the Boreal forest ecosystem of central Sweden

Energy Technology Data Exchange (ETDEWEB)

Fawaris, B H

1996-12-31

Behaviour of Chernobyl fallout 1{sup 37}Cs in a coniferous forest ecosystem in central Sweden was investigated between 1990 and 1994. Results demonstrated that forest soil belongs to nutrient deficient type, and deposited fallout 1{sup 37}Cs from Chernobyl nuclear accident (CNA) was retained in the upper 5 cm of humic forest soil layer, with a venial migration deeper into soil profile. No correlation between forest soil exchangeable and total potassium (K{sup +}) and 1{sup 37}Cs transfer parameters was observed. However, addition of K{sup +}, found to efficiently reduce 1{sup 37}Cs uptake by sheep`s fescue and the addition of stable caesium (1{sup 33}Cs{sup +}) enhanced it. The addition of ammonium (NH{sub 4}{sup +}) was slightly stimulating the uptake of 1{sup 37}Cs by sheep`s fescue in the first cut only. Field plants showed a considerably reduction in their 1{sup 37}Cs activity concentrations. Relative to their 1{sup 37}Cs levels of 1986-89, a little reduction in heather occurred eight years after CNA. In contrast the reductions in lingonberry and bilberry were 87% and 68%, respectively. Three fractions of forest soil bound 1{sup 37}Cs were observed due to sequential extraction procedure (SEP). The first, is easily extractable 1{sup 37}Cs fraction, it comprises 22% of total forest soil 1{sup 37}Cs inventory in the upper 5 cm layer. The second, is soil organically and biologically bound 1{sup 37}Cs comprises about 30% of soil bound 1{sup 37}Cs. This fraction might be accounted for long-term soil available 1{sup 37}Cs for plant uptake after bio-degradation processes by soil microorganisms. The third, is the residual fraction, it comprises more than 35% of total forest soil 1{sup 37}Cs inventory, and may be associated with soil components which are probably of organic nature. Sorption of 1{sup 37}Cs by zeolite (Mordenite) revealed that soil bound 1{sup 37}Cs is to some extent more mobile in forest soils with high OM% and low pH than those with low OM%.

Cs-137 migration in soil near NPPs

International Nuclear Information System (INIS)

Silant'ev, A.N.; Shkuratova, I.G.; Khatskevich, R.N.

1984-01-01

A convective-diffusion model has been employed for describing Cs-137 migration in soil. The migration parameters were determined by comparing the calculated vertical distribution profiles with the experimental ones. The migration parameters dependence on the soil state has been studied. Cs-137 penetration rate was found to be function of the soil type, surface state, soil wetness and orography. The obtained values are presented. A method is suggested for revealing the soil surface contamination by Cs-137 produced during NPP operation with distinguishing it from the global contamination background. For this purpose Cs-137 content in the upper 5 mm soil layer is estimated [ru

The accumulation of 137Cs in the biological compartment of forest soils

International Nuclear Information System (INIS)

Nikolova, Ivanka; Johanson, Karl J.; Clegg, Stephen

2000-01-01

Soil samples were collected in various forest stands, located about 40 km north-west from Uppsala. The various stands were: (1) Clear cut area made in 1987, (2) Normal forest with 50-100 old Norway spruce and Scots pine and with a thick humic layer of about 10 cm; (3) Raised bog with 50-year-old Scots pine and Sphagnum moss layer over peat soil. (4) Rocky area with old Scots pine, growing on a shallow soil, mainly of organic origin. (5) Normal forest with nearly 100-year-old spruce and pine, growing a shallow humic layer over sandy soil. Soil blocks of about 20x20 cm and down to a depth of 10-15 cm were collected on each site. The soil samples were mechanically separated into various fractions: bulk, rhizosphere and soil-root interface. The results showed that 137 Cs was unevenly distributed between the three soil fractions. The highest activity concentrations -- 3-4 times higher than in the other two fractions -- as well as the highest organic content -- usually more than 95% -- were found in the soil-root interface fraction. Of the total 137 Cs activity in the soil, 18% as a mean value was found in the soil-root interface fraction. The results thus show that a substantial fraction of the 137 Cs in the soils in some way associated with the biological part of the soil, probably with the fungal component

Cs4PbBr6/CsPbBr3 Perovskite Composites with Near-Unity Luminescence Quantum Yield: Large-Scale Synthesis, Luminescence and Formation Mechanism, and White Light-Emitting Diode Application.

Science.gov (United States)

Chen, Yameng; Zhou, Yang; Zhao, Qing; Zhang, Junying; Ma, Ju-Ping; Xuan, Tong-Tong; Guo, Shao-Qiang; Yong, Zi-Jun; Wang, Jing; Kuroiwa, Yoshihiro; Moriyoshi, Chikako; Sun, Hong-Tao

2018-04-18

All-inorganic perovskites have emerged as a new class of phosphor materials owing to their outstanding optical properties. Zero-dimensional inorganic perovskites, in particular the Cs4PbBr6-related systems, are inspiring intensive research owing to the high photoluminescence quantum yield (PLQY) and good stability. However, synthesizing such perovskites with high PLQYs through an enviromentally friendly, cost-effective, scalable, and high-yield approach remains challenging, and their luminescence mechanisms has been elusive. Here, we report a simple, scalable, room-temperature self-assembly strategy for the synthesis of Cs4PbBr6/CsPbBr3 perovskite composites with near-unity PLQY (95%), high product yield (71%) and good stability, using low-cost, low-toxicity chemicals as precursors. A broad range of experimental and theoretical characterizations suggest that the high-efficiency PL originates from CsPbBr3 nanocrystals well passivated by the zero-dimensional Cs4PbBr6 matrix that forms based on a dissolution-crystallization process. These findings underscore the importance in accurately identifying the phase purity of zero-dimensional perovskites by synchrotron X-ray technique to gain deep insights into the structure-property relationship. Additionally, we demonstrate that green-emitting Cs4PbBr6/CsPbBr3, combined with red-emitting K2SiF6:Mn4+, can be used for the construction of WLEDs. Our work may pave the way for the use of such composite perovskites as highly luminescent emitters in various applications such as lighting, displays, and other optoelectronic and photonic devices.

Real-time underwater image enhancement: An improved approach ...

Indian Academy of Sciences (India)

1School of Mechatronics, CSIR-Central Mechanical Engineering Research Institute, Durgapur 713209, India. 2Robotics and ...... a general purpose computer with Intel core i3 processor, frequency 2.20 ... Adobe Photoshop CS4 software. Table 6. .... 1In general, vision (e.g. camera) aided navigation requires on-board real-.

Synthesis, structural and spectroscopic properties of acentric triple molybdate Cs{sub 2}NaBi(MoO{sub 4}){sub 3}

Energy Technology Data Exchange (ETDEWEB)

Savina, A.A. [Laboratory of Oxide Systems, Baikal Institute of Nature Management, SB RAS, Ulan-Ude 670047 (Russian Federation); Department of Chemistry, Buryat State University, Ulan-Ude 670000 (Russian Federation); Atuchin, V.V., E-mail: atuchin@isp.nsc.ru [Laboratory of Optical Materials and Structures, Rzhanov Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090 (Russian Federation); Functional Electronics Laboratory, Tomsk State University, Tomsk 634050 (Russian Federation); Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Solodovnikov, S.F. [Laboratory of Crystal Chemistry, Nikolaev Institute of Inorganic Chemistry, SB RAS, Novosibirsk 630090 (Russian Federation); Department of Natural Sciences, Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Solodovnikova, Z.A. [Laboratory of Crystal Chemistry, Nikolaev Institute of Inorganic Chemistry, SB RAS, Novosibirsk 630090 (Russian Federation); Krylov, A.S. [Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Maximovskiy, E.A. [Laboratory of Epitaxial Layers, Nikolaev Institute of Inorganic Chemistry, SB RAS, Novosibirsk 630090 (Russian Federation); Laboratory of Research Methods of Composition and Structure of Functional Materials, Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Molokeev, M.S. [Laboratory of Crystal Structure, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Oreshonkov, A.S [Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Department of Photonics and Laser Technology, Siberian Federal University, Krasnoyarsk 660079 (Russian Federation); Pugachev, A.M. [Laboratory of Condenced Matter Spectroscopy, Institute of Automation and Electrometry, SB RAS, Novosibirsk 90, 630090 (Russian Federation); and others

2015-05-15

New ternary molybdate Cs{sub 2}NaBi(MoO{sub 4}){sub 3} is synthesized in the system Na{sub 2}MoO{sub 4}–Cs{sub 2}MoO{sub 4}–Bi{sub 2}(MoO{sub 4}){sub 3}. The structure of Cs{sub 2}NaBi(MoO{sub 4}){sub 3} of a new type is determined in noncentrosymmetric space group R3c, a=10.6435(2), c=40.9524(7) Å, V=4017.71(13) Å{sup 3}, Z=12 in anisotropic approximation for all atoms taking into account racemic twinning. The structure is completely ordered, Mo atoms are tetrahedrally coordinated, Bi(1) and Bi(2) atoms are in octahedra, and Na(1) and Na(2) atoms have a distorted trigonal prismatic coordination. The Cs(1) and Cs(2) atoms are in the framework cavities with coordination numbers 12 and 10, respectively. No phase transitions were found in Cs{sub 2}NaBi(MoO{sub 4}){sub 3} up to the melting point at 826 K. The compound shows an SHG signal, I{sub 2w}/I{sub 2w}(SiO{sub 2})=5 estimated by the powder method. The vibrational properties are evaluated by Raman spectroscopy, and 26 narrow lines are measured. - Graphical abstract: - Highlights: • The crystal structure of Cs{sub 2}NaBi(MoO{sub 4}){sub 3} is defined. • The molybdate Cs{sub 2}NaBi(MoO{sub 4}){sub 3} is stable up to melting point at 826 K. • Vibrational properties of Cs{sub 2}NaBi(MoO{sub 4}){sub 3} are evaluated by Raman spectroscopy.

Effect of He pressure on the superconducting transition temperatures of Na2CsC60 and (NH3)4Na2CsC60

International Nuclear Information System (INIS)

Schirber, J.E.; Bayless, W.R.; Rosseinsky, M.J.; Zhou, O.; Fleming, R.M.; Murphy, D.; Fischer, J.E.

1994-01-01

The Na based mixed alkali doped C 60 superconductors show anomalous behavior with respect to the ''universal'' superconducting transition temperature T c vs lattice constant a 0 relation followed by most of the fcc A 3 C 60 superconductors. We have measured dt c /dP for Na 2 CsC 60 and (NH 3 ) 4 Na 2 CsC 60 using solid He as the pressure medium to ∼ 6 kbar finding dT c /dP equal to -0.8±(0.01) K/kbar and -1.0(±0.1)K/kbar for Na 2 CsC 60 and Na 2 (NH 3 ) 4 C 60 respectively. Our value for Na 2 CsC 60 differs markedly from that obtained by Mizuki et al of about -1.3 K/kbar. However, using N 2 or Ar, we obtain values for dT c /dP in substantial agreement with Mizuki et al who used fluorinert to generate their pressure. This work emphasizes the need for compressibility measurements with the same pressure medium in the appropriate temperature range so that meaningful comparisons can be made between various pressure measurements and models which are based on lattic spacing

137 Cs in the soil from Pljevlja region

International Nuclear Information System (INIS)

Vukotic, P.; Jovanovic, S.; Dapcevic, S.; Zic, J.

1996-01-01

Surface layer of the seven characteristic types of soil in Pljevlja region (Montenegro) is sampled. Soil samples are taken 33 locations, at eight of them from three layers up to 20 cm in depth. Specific activity of 137 Cs is then measured in the soil samples by a method of semiconductor gamma-spectrometry. Average cesium contamination in the region is found to be about 10 times higher than the same before Chernobyl accident. 137 Cs is still in the superficial soil layer, mostly to the depth of 10 cm. Contamination level of soil has certain regularities in distribution over the region, and is the highest on the two mutually almost parallel geographic directions. 7 refs.; 1 figs.; 1 tabs

Determination of Cs-134 and Cs-137 rain water samples

International Nuclear Information System (INIS)

Lima, M.F.; Mazzilli, B.

1988-01-01

In order to setting an environmental monitoring program at IPEN, was developed a fast and simple methodology for concentration of Cs-134 and Cs-137 in rain water. This procedure consists in the precipitation of cesium and others cathions of its family (NH 4 + , K + and Rb + ) by ammonium molybdophosphate. The measures of the desintegration rates of Cs-134 and Cs-137 was done by gamma spectrometry in a Ge(Li) detector. After setting up the ideal experimental conditions, the procedure was used to analyze four samples of rain water. (author) [pt

Agreement between clinical estimation and a new quantitative analysis by Photoshop software in fundus and angiographic image variables.

Science.gov (United States)

Ramezani, Alireza; Ahmadieh, Hamid; Azarmina, Mohsen; Soheilian, Masoud; Dehghan, Mohammad H; Mohebbi, Mohammad R

2009-12-01

To evaluate the validity of a new method for the quantitative analysis of fundus or angiographic images using Photoshop 7.0 (Adobe, USA) software by comparing with clinical evaluation. Four hundred and eighteen fundus and angiographic images of diabetic patients were evaluated by three retina specialists and then by computing using Photoshop 7.0 software. Four variables were selected for comparison: amount of hard exudates (HE) on color pictures, amount of HE on red-free pictures, severity of leakage, and the size of the foveal avascular zone (FAZ). The coefficient of agreement (Kappa) between the two methods in the amount of HE on color and red-free photographs were 85% (0.69) and 79% (0.59), respectively. The agreement for severity of leakage was 72% (0.46). In the two methods for the evaluation of the FAZ size using the magic and lasso software tools, the agreement was 54% (0.09) and 89% (0.77), respectively. Agreement in the estimation of the FAZ size by the lasso magnetic tool was excellent and was almost as good in the quantification of HE on color and on red-free images. Considering the agreement of this new technique for the measurement of variables in fundus images using Photoshop software with the clinical evaluation, this method seems to have sufficient validity to be used for the quantitative analysis of HE, leakage, and FAZ size on the angiograms of diabetic patients.

Differential bioaccumulation of "1"3"4Cs in tropical marine organisms and the relative importance of exposure pathways

International Nuclear Information System (INIS)

Metian, Marc; Pouil, Simon; Hédouin, Laetitia; Oberhänsli, François; Teyssié, Jean-Louis; Bustamante, Paco; Warnau, Michel

2016-01-01

Bioaccumulation of "1"3"4Cs was determined in 5 tropical marine species: three bivalves (the oysters Isognomon isognomum and Malleus regula, and the clam Gafrarium pectinatum), one decapod (shrimp Penaeus stylirostris) and one alga (Lobophora variegata). Marine organisms were exposed to the radionuclides via different pathways: seawater (all of them), food (shrimp and bivalves) and sediment (bivalves). Our results indicate that the studied tropical species accumulate Cs similarly than species from temperate regions whereas retention capacities seems to be greater in the tropical species. Bioaccumulation capacities of the two oysters were similar for all the exposure pathways. The alga, and to a lesser extent the shrimp, concentrated dissolved Cs more efficiently than the bivalves (approx. 14 and 7 times higher, respectively). Assimilation efficiencies of Cs in bivalves and shrimp after a single feeding with radiolabelled food were comprised between 7.0 ± 0.4 and 40.7 ± 4.3%, with a variable retention time (half-life –T_b_1_/_2– ranging from 16 ± 3 to 89 ± 55 d). Although the clam lives buried in the sediment, this exposure pathway resulted in low bioaccumulation efficiency for sediment-bound Cs (mean transfer factor: 0.020 ± 0.001) that was lower than the two oyster species, which are not used to live in this media (0.084 ± 0.003 and 0.080 ± 0.005). Nonetheless, Cs accumulated from sediment was similarly absorbed (61.6 ± 9.7 to 79.2 ± 2.3%) and retained (T_b_1_/_2: 37 ± 2 to 58 ± 25 d) for the three bivalves species. Despite the poor transfer efficiency of Cs from food, the use of a global bioaccumulation model indicated that the trophic pathways was the main uptake route of Cs in the bivalves and shrimp. In shelled organisms, shells played a non-negligible role in Cs uptake, and their composition and structure might play a major role in this process. Indeed, most of the Cs taken up from seawater and sediment was principally

Crystal field effect in the uranium compounds - model calculations for CsUF6, Cs2UCl6 and UCl4

International Nuclear Information System (INIS)

Gajek, Z.; Mulak, J.

1987-01-01

A practical crystal field model allowing one to estimate the crystal field parameters from first principles is presented and applied to the actinide compounds. The model results directly from the renormalization (and reduction) procedure of the true Schroedinger equation for an effective Hamiltonian acting on the 5f spin-orbitals only. In practice this approach becomes convergent with the ab initio model of Newman. Three ionic uranium compounds: CsUF 6 , Cs 2 UCl 6 and UCl 4 have served as examples of the application. The results obtained, particularly for the first two compounds, are in good agreement with the experimental data. The contributions of different mechanisms responsible for the crystal field effect are discussed. (author)

Systems of Na/sup +/NO/sub 3/, Na/sub 2/SO/sub 4/, RbNO/sub 3/, Rb/sub 2/SO/sub 4/-H/sub 2/O and NaNO/sub 3/, Na/sub 2/SO/sub 4/, CsNO/sub 3/, Cs/sub 2/SO/sub 4/-H/sub 2/O at 25 and 75 deg C

Energy Technology Data Exchange (ETDEWEB)

Poletaev, I F; Krasnenkova, L V

1975-08-01

Quaternary Na/sup +/, Rb/sup +///NO/sub 3/-, SO/sub 4//sup 2 -/-H/sub 2/O and Nsub(+), Cs/sup +///NO/sub 3/-, SO/sub 4//sup 2 -/-H/sub 2/O mutual systems have been studied isothermally. The following six fields of crystallization have been revealed in these systems at 25 deg C: Cs/sub 2/SO/sub 4/, Na/sub 2/SO/sub 4/, Na/sub 2/SO/sub 4/x10H/sub 2/O, NaNO/sub 3/xNa/sub 2/SO/sub 4/x2H/sub 2/O, NaNO/sub 3/, and CsNO/sub 3/.

{sup 137}Cs in northern Adriatic sediments

Energy Technology Data Exchange (ETDEWEB)

Barisic, D; Lulic, S; Vdovic, N; Vertacnik, A [Center for Marine Research - Department Zagreb, ' Ruder Boskovic' Institute, Zagreb (Croatia); Juracic, M [Department of Geology, Faculty of Natural Sciences, University of Zagreb, Zagreb (Croatia)

1996-01-01

The activity of {sup 137}Cs in shallow northern Adriatic sediments was obtained on the basis of measurement results from 25 sediment box cores, sampled during the Adriatic Scientific COoperation Program (ASCOP) 16 cruise in the summer 1990. {sup 137}Cs was determined in surface sediments (0-3 cm) and 12-15 cm-deep sediment. It was found that the lowest caesium concentrations correspond to sands, which are spread along the Croatian coast. Parallel to the Italian coast, {sup 137}Cs concentrations in pelites are the highest. It seems that the influence of Po River is significant for {sup 137}Cs activities in recent marine sediments along Italian coast south of Po River delta. Significantly higher {sup 137}Cs activities in 0-3 cm sediment layer can be attributed to the deposition caused by Chernobyl accident. (author)

Electron dynamics of Cs covered Cu(111). A scanning tunneling spectroscopy inverstigation at low temperatures

International Nuclear Information System (INIS)

Hofe, T. von

2005-01-01

During this Ph.D. a scanning tunneling microscope operating in ultra-high vacuum and at low temperatures was assembled and modified to allow operation at variable temperatures. Also, an additional vibration isolation stage was conceived and mounted. Measurements were performed on Cu(111)-Cs for different coverages. For a coverage of Θ=0:05 ML, the layer shows a commensurate (√(19) x √(19)R23.4 ) structure which may be stabilized by surface-state mediated adatom interactions. For higher coverages, the layer is incommensurate and rotated with respect to the substrate, where the angle of rotation depends on the coverage. At the saturation coverage Θ=0:25 ML, the layer, although commensurate, reveals many defects. The binding energy of the quantum well state (QWS) confined to the Cs layer decreases with increasing coverage as has been observed before for other systems. The lifetime of the QWS decreases with increasing binding energy. The comparatively short lifetime for Cu(111)-p(2 x 2)Cs led to the introduction of Brillouin Zone Backfolding as a new lifetime-limiting process. Acquisition of dispersion relations of the QWS for different coverages revealed that the effective mass of the excitations increases with decreasing binding energy. (Orig.)

X-ray detection capability of a Cs2ZnCl4 single-crystal scintillator

International Nuclear Information System (INIS)

Yahaba, Natsuna; Koshimizu, Masanori; Sun, Yan; Asai, Keisuke; Yanagida, Takayuki; Fujimoto, Yutaka; Haruki, Rie; Nishikido, Fumihiko; Kishimoto, Shunji

2014-01-01

The X-ray detection capability of a scintillation detector equipped with a Cs 2 ZnCl 4 single crystal was evaluated. The scintillation decay kinetics can be expressed as the sum of two exponential decay components. The fast decay component had a decay time constant of 1.8 ns, and its relative intensity was 95%. The total light output was 630 photons/MeV, and a subnanosecond timing resolution of 0.66 ns was obtained. The detection efficiency of 67.4 keV X-rays was 80% for a detector equipped with a 2.2-mm-thick Cs 2 ZnCl 4 crystal. Thus, excellent timing resolution and high detection efficiency were achieved simultaneously. (author)

The behavior of radioactive 137Cs and stable Cs at the isolated undisturbed mountain pond in Fukui, Japan

International Nuclear Information System (INIS)

Iwamoto, Kazumi; Kimura, Makio; Ando, Kenji; Amano, Hikaru

2003-01-01

The behavior of radioactive 137 Cs and stable Cs at the isolated undisturbed mountain pond in Fukui, Japan was studied for the pond water, the sedimentary grains and the soil near the pond. The concentrations of 137 Cs and stable Cs in the pond water ranged from 0.23 to 0.85 Bq/m 3 and from 0.005 to 0.018 mg/m 3 , respectively. The sedimentary grains were sorted by sieving into fractions with diameter from 2 mm to less than 38 μm. The concentrations of 137 Cs and stable Cs in the sorted grains were measured, and those of the adsorbed state were determined by subtracting the concentration of the grain matrix. The adsorbed concentrations increased with decrease in particle diameter and depended less on the kind of samples. The in-situ distribution coefficient Kd depended largely on particle diameter and increased with the decrease in diameter. The values of Kd ranged from about 20 to 1200 m 3 /kg for stable Cs and about 15 to 1000 m 3 /kg for 137 Cs, and the Kd of 137 Cs seemed to be slightly smaller than that of stable Cs. The concentration of stable Cs in the sedimentary mud was found to be close to that of the fine grains. The concentrations of stable Cs in the soil near the pond was about 7.7 mg/kg, and that of 137 Cs was about 0.6 kBq/kg for the surface layer soil and decreased with increase in soil depth. (author)

Progress in ultrafast CsI-photocathode gaseous imaging photomultipliers

International Nuclear Information System (INIS)

Dagendorf, V.; Breskin, A.; Chechick, R.; Schmidt-Boecking, H.

1991-04-01

A large area low-pressure gas-filled UV-imaging photomultiplier with CsI photocathode is presented. The double step electron photomultiplier with a 10 torr CH 4 gas-filling enables stable high gain operation. The detection efficiency of photon in the wavelength range λ ∼ 170 nm (Xe scintilation light) is about 10% for 200 to 2000 nm thick photocathodes. We investigate the influence of various substrate materials, the thickness of the CsI-layer, the gas pressure and the gas composition on the performance of the photocathode. Furthermore we studied the stability of the photocathode under different operating conditions and its sensitivity to air. Measurements of the timing characteristic of the device yielded an ultimate time resolution of 350 ps (fwhm). (author)

137Cs concentration distribution in among feeds and various soil types

International Nuclear Information System (INIS)

Csupka, S.

1980-01-01

The distribution of 137 Cs in four types of arable land and soil with grass cover (chernozem, serozem, gely soddy soil and meadow calcareous soil) is different. In arable land the penetration of 137 Cs into greater depths is higher than under the grasscover, where the main proportion of 137 Cs is retained by the upper layers in the depth of 0 to 5 cm. The only exception is gley soddy soil, where the upper layers allow the passage of radionuclides into greater depths. In the soil horizon to a depth of 50 cm out or the total content of 137 Cs from 16 to 47% is bound in exchangeable form and from 53 to 84% in a form available to plants according to the soil type. The relationship between exchangeable 137 Cs and that available to plants in soils is given by the coefficient of desorption and the relation between the 137 Cs content in the plant and in the soil is given by the coefficient of concentration. Their value varies within the range of 0.1 to 2.6. (author)

The Status of GLAST CsI Calorimeter

Energy Technology Data Exchange (ETDEWEB)

Chekhtman, A.

2003-09-18

GLAST is a gamma-ray observatory for celestial sources in the energy range from 20 MeV to 300 GeV. This is NASA project with launch anticipated in 2006. The principal instrument of the GLAST mission is the Large Area Telescope (LAT), consisting of an Anti Coincidence Detector (ACD), a silicon-strip detector Tracker (TKR) and a hodoscopic CsI Calorimeter (CAL). It consists of 16 identical modules arranged in a 4 x 4 array. Each module has horizontal dimensions 38 x 38 cm{sup 2} and active thickness 8.5 radiation length. It contains 96 CsI (Tl) crystals arranged in 8 layers with 12 crystals per layer. The scintillation light is measured by PIN photodiodes mounted on both ends of each crystal. The sum of signals at the two ends of the crystal provides the energy measurement. The difference in these signals provides the position measurement along the crystal. The calorimeter was designed to meet the goals of good energy resolution (better than 10% for photon energies 100 MeV-100 GeV), position resolution of {approx} 1 mm for photon energies > 1 GeV, and a rejection factor of > 100 for charged cosmic rays, under limitations on calorimeter weight (95 kg per module) and power consumption (6 W per module). The Monte Carlo simulation and prototype beam test results confirm that proposed design meets the requirements. Calorimeter production is planned to start in 2003.

Quasi-self-trapped Frenkel-exciton near-UV luminescence with large Stokes shift in wide-bandgap Cs4PbCl6 nanocrystals

Science.gov (United States)

Zhang, Yumeng; Fan, Baolu; Liu, Yuzhen; Li, Hongxia; Deng, Kaiming; Fan, Jiyang

2018-04-01

Inorganic lead halide perovskite nanocrystals (NCs) have attracted great interest owing to their superior luminescence and optoelectronic properties. In comparison to cubic CsPbX3 (X = Cl, Br, or I) that has visible luminescence, trigonal Cs4PbX6 has a much larger bandgap and distinct optical properties. Little has been known about the luminescence properties of the Cs4PbX6 NCs. In this study, we synthesize the well-crystallized Cs4PbCl6 NCs with sizes of 2.2-11.8 nm, which exhibit stable and near-UV luminescence (with a lifetime of 19.7-24.2 ns) with a remarkable quantum confinement effect at room temperature. In comparison to the negligible Stokes shift in the CsPbCl3 NCs, the Stokes shift of the Cs4PbCl6 NCs is very large (0.91 eV). The experimental results in combination with the first-principles calculations reveal that the near-UV luminescence of the Cs4PbCl6 NCs stems from the Frenkel excitons self-trapped in the isolated PbCl64- octahedrons. This is different from the CsPbCl3 NCs whose luminescence originates from the free Wannier excitons. The theoretical model based on the lattice relaxation is proposed to account for the large Stokes shift and its abnormal decrease with the decreasing particle size.

Redetermination of the cubic struvite analogue Cs[Mg(OH26](AsO4

Directory of Open Access Journals (Sweden)

Matthias Weil

2009-01-01

Full Text Available In contrast to the previous refinement from photographic data [Ferrari et al. (1955. Gazz. Chim. Ital. 84, 169–174], the present redetermination of the title compound, caesium hexaaquamagnesium arsenate(V, revealed the Cs atom to be on Wyckoff position 4d instead of Wyckoff position 4b of space group Foverline{4}3m. The structure can be derived from the halite structure. The centres of the complex [Mg(OH26] octahedra and the AsO4 tetrahedra (both with overline{4}3m symmetry are on the respective Na and Cl positions. The building units are connected to each other by O—H...O hydrogen bonds. The Cs+ cations (overline{4}3m symmetry are located in the voids of this arrangement and exhibit a regular cuboctahedral 12-coordination to the O atoms of the water molecules. The O atom bonded to As has 2mm site symmetry (Wyckoff position 24f and the water-molecule O atom has m site symmetry (Wyckoff position 48h.

Crystal structures of LiCsTiF6 and Cs2TiF6 and interval mobility of complex anions

International Nuclear Information System (INIS)

Popov, D.Yu.; Kavun, V.Ya.; Gerasimenko, A.V.; Sergienko, V.I.; Antokhina, T.F.

2002-01-01

The structure of LiCsTiF 6 (1) and Cs 2 TiF 6 (2) monocrystals was studied by the method of X-ray diffraction analysis. Crystal lattice parameters for compound 1 are: a = 9.251 (1), b = 11.920 (1), c = 10.271 (1), sp.gr. Pbcn, Z = 8; for compound 2: a = 6.213 (1), c = 5.004 (1), sp.gr. P3-bar m1, Z = 1. Three-dimensional frame of bound titanium octahedrons and slightly distorted lithium tetragonal pyramids with Li-F distance ranging from 1.86 to 2.24 A is the crystal structure base of compound 1. The structure of compound 2 is made of dose-packed CsF 3 layers and TiF 6 2- octahedrons located between the layers. The types of internal motion of the complex anions were determined by 10 F NMR method, their activation energy in crystals 1 and 2 in the temperature range of 200-500 K being estimated [ru

Cs2SO4-Pr2(SO4)3-H2O and NiSO4-Pr2(SO4)3-H2O systems at 75 deg C

International Nuclear Information System (INIS)

Onishchenko, M.K.; Skorikov, V.M.; Shevchuk, V.G.; AN SSSR, Moscow. Inst. Obshchej i Neorganicheskoj Khimii)

1979-01-01

To investigate physico-chemical properties of equilibrium saturated solutions and to elucidate the chemical changes under way, the aqueous systems of cesium, nickel and praseodymium (3) sulfates are studied. The method of isothermal saturation of salts at 75 deg C is used. It has been found that in the system Cs 2 SO 4 -Pr 2 (SO 4 ) 3 -H 2 O in a wide concentration range the soluble binary salt Cs 2 SO 4 xPr 2 (SO 4 ) 3 csytallizes in a congruent way. For the system NiSO 4 -Pr 2 (SO 4 ) 3 -H 2 O a solubility curve of the eutonic type is obtained, there being no chemical interaction between the components. The solubility isotherms for the system are given

Ternary system of Na2MoO4-Cs2MoO4-MoO3

International Nuclear Information System (INIS)

Zueva, V.P.; Shabanova, A.N.; Drobasheva, T.I.

1982-01-01

Using the methods of thermal analysis interaction of components in ternary system Na 2 MoO 4 -Cs 2 MoO 4 -MoO 3 has been studied. Crystallization surface consists of nine fields belonging to initial components and compounds of lateral sides. Triangulation of the system is carried out and the character of nonvariant points is clarified, the temperature of 360 deg C corresponds to low-melting eutectics

Pure Cs4PbBr6: Highly Luminescent Zero-Dimensional Perovskite Solids

KAUST Repository

Saidaminov, Makhsud I.; Almutlaq, Jawaher; Sarmah, Smritakshi P.; Dursun, Ibrahim; Zhumekenov, Ayan A.; Begum, Raihana; Pan, Jun; Cho, Nam Chul; Mohammed, Omar F.; Bakr, Osman

2016-01-01

more than 2 orders of magnitude lower PLQY. Such a PLQY of Cs4PbBr6 is significantly higher than that of other solid forms of lower-dimensional metal halide perovskite derivatives and perovskite nanocrystals. We attribute this dramatic increase in PL

The hydrogen dynamics of CsH5(PO4)2 studied by means of nuclear magnetic resonance

International Nuclear Information System (INIS)

Gradisek, A; Dimnik, B; Vrtnik, S; Dolinsek, J; Wencka, M; Zdanowska Fraczek, M; Lavrova, G V

2011-01-01

We have investigated the hydrogen dynamics of cesium pentahydrogen diphosphate, CsH 5 (PO 4 ) 2 , by means of nuclear magnetic resonance (NMR) spectroscopy, in order to address the question of why there is no superprotonic phase transition in this compound, in contrast to other structurally similar hydrogen-bonded ionic salts, where a superprotonic transition is frequently found to be present. The analysis of the NMR spectrum and the spin-lattice relaxation rate revealed that the temperature-dependent hydrogen dynamics of CsH 5 (PO 4 ) 2 involves motional processes (the intra-H-bond jumps and the inter-H-bond jumps at elevated temperatures, as a mechanism of the ionic conductivity) identical to those for the other H-bonded superprotonic salts. The considerably stronger H-bond network in CsH 5 (PO 4 ) 2 prompts the search for a higher superprotonic transition temperature. However, due to the relatively weak bonding between the {[H 2 PO 4 ]} ∞ planes in the [100] direction of the CsH 5 (PO 4 ) 2 structure by means of the ionic bonding via the cesium atoms and the small number of H bonds in that direction (where out of five H bonds in the unit cell, four are directed within the {[H 2 PO 4 ]} ∞ planes and only one is between the planes), the bonds between the planes become thermally broken and the crystal melts before the H-bond network rearranges via water release into an open structure typical of the superprotonic phase. Were the coupling between the {[H 2 PO 4 ]} ∞ planes in the CsH 5 (PO 4 ) 2 somewhat stronger, the superprotonic transition would occur in the same manner as it does in other structurally related hydrogen-bonded ionic salts.

Radiocesium migration in the litter layer of different forest types in Fukushima, Japan.

Science.gov (United States)

Kurihara, Momo; Onda, Yuichi; Kato, Hiroaki; Loffredo, Nicolas; Yasutaka, Tetsuo; Coppin, Frederic

2018-07-01

Cesium-137 ( 137 Cs) migration in the litter layer consists of various processes, such as input via throughfall, output via litter decomposition, and input from deeper layers via soil organism activity. We conducted litter bag experiments over 2 years (December 2014-November 2016) to quantify the inputs and outputs of 137 Cs in the litter layer in a Japanese cedar plantation (Cryptomeria japonica) and a mixed broadleaf forest dominated by Quercus serrata located 40 km northwest of the Fukushima Dai-ichi Nuclear Power Plant. The experiments included four conditions, combining contaminated and non-contaminated litter and deeper layer material, and the inputs and outputs were estimated from the combination of 137 Cs increases and decreases in the litter layer under each condition. The 137 Cs dynamics differed between the two forests. In the C. japonica forest, some 137 Cs input via throughfall remained in the litter layer, and downward 137 Cs flux passed through the litter layer was 0.42 (/year).Upward flux of 137 Cs from the deeper layer was very restricted, layers was restricted, downward 137 Cs flux was less than 0.003 (/year).Upward input of 137 Cs from the deeper layer was prominent, 0.037 (/year). 137 Cs output via litter decomposition was observed in both forests. The flux in the C. japonica forest was slower than that in the broadleaf forest, 0.12 and 0.15 (/year), respectively. Copyright © 2018 Elsevier Ltd. All rights reserved.

Theoretical study of the Cs isotope exchange reaction of CsI + Cs' → Cs + ICs' (Contract research)

International Nuclear Information System (INIS)

Kobayashi, Takanori; Hashimoto, Masashi; Yokoyama, Keiichi

2015-12-01

To discuss the exchange reaction of Cs isotope by CsI + Cs' → Cs + ICs', the structure and chemical properties of Cs 2 I intermediate and potential energy surface of the entrance reaction are calculated using M06/def2-TZVPPD density functional calculation. The calculation shows that the reaction to the intermediate has no barrier and the two Cs-I bonds of Cs 2 I are chemically equivalent. These results suggest that the rate of the Cs exchange reaction of CsI + Cs' → Cs + ICs' is as high as the collision rate. (author)

Radiation damage in undoped CsI and CsI(Tl)

International Nuclear Information System (INIS)

Woody, C.L.; Kierstead, J.A.; Levy, P.W.; Stoll, S.

1992-01-01

Radiation damage has been studied in undoped CsI and CsI(TI) crystals using 60 Co gamma radiation for doses up to ∼ 4.2 x 10 6 . Samples from various manufacturers were measured ranging in size from 2.54 cm long cylinders to a 30 cm long block. Measurements were made on the change in optical transmission and scintillation light output as a function of dose. Although some samples showed a small change in transmission, a significant change in light output was observed for all samples. Recovery from damage was also studied as a function of time and exposure to UV light. A short lived phosphorescence was observed in undoped CsI, similar to the phosphorescence seen in CsI(TI)

Trends in Illustration: A digital approach to large format illustrations ...

African Journals Online (AJOL)

In view of this, this study uses Adobe Photoshop CS4, a digital draw and paint tool, to illustrate some of the notable folktales in Igbo oral tradition. Vector and Raster techniques of computer graphics will be employed and discussed. Basic information on digital illustration will also be enumerated in the project. This piece of ...

Vandmølle i Tadami

DEFF Research Database (Denmark)

2016-01-01

in black color. The image shows part of a texture map, which belongs to a 3d modelled fragment of a watermill recorded in Tadami, Japan. The 3d model and texture map are captured on an iPhone 4S using photogrammetry in a digital process implemented with 123D Catch from Autodesk and Adobe Photoshop CS6...

(134)Cs and ¹³⁷Cs levels in a grassland, 32 km northwest of the Fukushima 1 Nuclear Power Plant, measured for two seasons after the fallout.

Science.gov (United States)

Terashima, Ichiro; Shiyomi, Masae; Fukuda, Hiroo

2014-01-01

We measured the levels of radioactive caesium (RACs; ¹³⁴Cs and ¹³⁷Cs) in plants and soil in a grassland, 32 km northwest of the Fukushima 1 Nuclear Power Plant, from June 2011 to October 2012. In 2011, the highest RACs levels (¹³⁴Cs + ¹³⁷Cs) in plants and in the 0-5 cm soil layer were approximately 80 kBq per kg dry weight (DW). Forage grasses and clovers in this grassland showed similar RACs levels. On a DW basis, the levels of RACs in these plants tended to increase with increasing biomass over both years, but the absolute levels decreased in 2012. The RACs levels in the soil decreased sharply with soil depth; the RACs level in the 5-10 cm soil layer was only 3 % of that in the 0-5 cm layer. The transfer factor (ratio of radioactivity in plant parts on DW basis to that in the 0-10 cm soil layer) was 0.5 and 1.0 for the aboveground and belowground plant parts, respectively, in 2011, and these values decreased by approximately 50 % in 2012. We discuss the possible mechanisms underlying these trends, and strategies to decrease the level of RACs in plants to the permissible level for forage.

CsPb2Br5 Single Crystals: Synthesis and Characterization

KAUST Repository

Dursun, Ibrahim; de Bastiani, Michele; Turedi, Bekir; Alamer, Badriah Jaber; Shkurenko, Aleksander; Yin, Jun; Gereige, Issam; Alsaggaf, Ahmed; Mohammed, Omar F.; Eddaoudi, Mohamed; Bakr, Osman

2017-01-01

, which enabled us to finally clarify the material's optical features. Our CsPb2Br5 crystal has a two-dimensional structure with Pb2Br5- layers spaced by Cs+ cations, and exhibits a ~3.1 eV indirect bandgap with no emission in the visible spectrum.

Energy spectrum of CsDy(MoO/sub 4/)/sub 2/ in the vicinity of the structural phase transition

Energy Technology Data Exchange (ETDEWEB)

Khats' ko, E N; Chernyj, A S [AN Ukrainskoj SSR, Kharkov. Fiziko-Tekhnicheskij Inst. Nizkikh Temperatur

1981-08-01

The magnetic susceptibilities of CsDy(MoO/sub 4/)/sub 2/ and CsDy(MoO/sub 4/)/sub 2/+10%Eu/sup 3 +/ were measured in the temperature range 4 to 70 K and the frequency range 200 Hz to 20 MHz. The observed spin-lattice relaxation of the Dy/sup 3 +/ ion is found to be exponential with the relaxation time as a function of temperature tau/sup -1/=A exp (-..delta../kT) with ..delta..=105+-20 and 250+-40 cm/sup -1/ for CsDy(MoO/sub 4/)/sub 2/ in ranges 10-20 K and 20-38 K, respectively, and ..delta..=22.4+-5 cm for C=sDy(MoO/sub 4/)/sub 2/+10%Eu/sup 3 +/. The energies ..delta..105+-20 and 250 -40cm/sup -1/ are suggested to correspond to the first and second excited levels of Dy/sup 3 +/ in the low temperature phase of CsDy(MoO/sub 4/)/sub 2/, and ..delta..=22.4+-5 cm/sup -1/ to the first excited level of Dy/sup 3 +/ in the high temperature phase of the compound.

Design and synthesis of a redox-active tc-99m radiopharmaceutical with ferrocenedithiocarboxylate [FcCS=Fe(C{sub 5}H{sub 4}CS{sub 2})(C{sub 5}H{sub 5}){sup -}

Energy Technology Data Exchange (ETDEWEB)

Uccelli, Licia; Bolzati, Cristina; Boschi, Alessandra; Duatti, Adriano E-mail: dta@ifeuniv.unife.it; Morin, Christophe; Pasqualini, Roberto; Giganti, Melchiore; Piffanelli, Adriano

1999-01-01

The synthesis, at tracer level, of two Tc-99m complexes having the same chemical composition and structure, but differing by one electron in the total electron counting, is reported. These compounds have been prepared by reacting [{sup 99m}TcO{sub 4}]{sup -} with the piperidinium salt of the ligand ferrocenedithiocarboxylate {l_brace}[Fe(II)(C{sub 5}H{sub 4}CS{sub 2})(C{sub 5}H{sub 5})]{sup -}=FcCS{r_brace}, in the presence of N-methyl S-methyldithiocarbazate as donor of N{sup 3-} groups, and triphenylphosphine or SnCl{sub 2} as reducing agents. The formation of the neutral complex [{sup 99m}Tc(N)(FcCS){sub 2}] (compound A) and of the monocationic, mixed-valence complex [{sup 99m}Tc(N)(FcCS) (FcCS*)]{sup +} (compound B) {l_brace}FcCS* [Fe(III)(C{sub 5}H{sub 4}CS{sub 2})(C{sub 5}H{sub 5})]{r_brace} was obtained in high yield. Both complexes comprise a terminal Tc{identical_to}N multiple bond and two FcCS ligands coordinated to the metal center through the two sulfur atoms of the -CS{sub 2} group, but they differ in the oxidation state of one of the two iron atoms of the coordinated FcCS ligands. In complex A, the two Fe atoms are both in the +2 oxidation state, while in B, one Fe atom is in the +2 and the other is in the +3 oxidation state. Thus, B is a mixed-valence Fe(II)-Fe(III) complex. B is easily converted into A by one-electron exchange with various reductants such as triphenylphosphine and excess SnCl{sub 2}. Biodistribution studies in rats showed that complexes A and B are mostly retained in lungs and liver without any significant uptake in organs such as heart and brain.

Theoretical study on decay of the 4d core-excited states of Cs III

International Nuclear Information System (INIS)

Ding Xiaobin; Dong Chenzhong; Fritzsche, Stephan

2008-01-01

In a recent XUV photoabsorption spectrum of Cs III ions by Cummings and O'Sullivan [2001 J. Phys. B 34 199], rather large linewidths were found for the 4d 9 5s 2 5p 6 – 4d 10 5s 2 5p 5 transition which are quite in disagreement with corresponding quasi-relativistic multiconfiguration Hartree–Fock (MCHF) calculation. In the present work, a detailed multiconfiguration Dirac-Fock study has been carried out to explore this discrepancy. Owing to the detailed consideration of electron correlation effects, some 'forbidden' Auger decay channels, such as 4d 10 5s 2 5p 3 5d and 4d 10 5s 0 5p 6 , would become 'open'. As a result, remarkable improvement of the linewidths has been obtained in our calculation. Furthermore, the theoretical Auger spectrum of the 4d 9 5s 2 5p 6 core-excited states of Cs III ions is given in the present work

Synthesis and crystal structure of hydrogen phosphites RbH2PO3, CsH2PO3, and TlH2PO3

International Nuclear Information System (INIS)

Kosterina, E.V.; Troyanov, S.I.; Kemnits, Eh.; Aslanov, L.A.

2001-01-01

The crystal acid phosphites RbH 2 PO 3 , CsH 2 PO 3 and TlH 2 PO 3 were separated during reaction of Rb, Cs and Tl carbonates with phosphorous acid solution. The crystal structure of the compounds was analyzed by X-ray diffraction method at 150 K. CsH 2 PO 3 has a monoclinic system, a = 7.930(2), b = 8.929(2), c = 13.163(3) A, β = 104.84(3) Deg, V = 900.9(4) A 3 , Z 8, sp. gr. P2 1 /c, R 1 = 0.239. In the structure hydrogen bonds integrate the PHO 3 tetrahedrons in the unlimited zigzag chains [HPHO 3 ] n n- laying at the layers, which are alternate to the layers of metal cations. The layers of anion chains have a wavy form [ru

Photoelectron extraction efficiency from a CsI photocathode and THGEM operation in He−CF4 and He−CH4 mixtures

International Nuclear Information System (INIS)

Coimbra, A.E.C.; Santos, J.M.F. dos; Israelashvili, I.

2016-01-01

This work presents the experimental measurements obtained for UV-induced photo-electron extraction efficiency from a CsI photocathode into He with CF 4 and CH 4 gas mixtures. A 1000Å CsI photocathode was deposited on a gold plated THGEM for photo-electron conversion. Charge-gain measurements were obtained with a Single-THGEM detector operating in these gas mixtures using a continuous UV lamp for the extraction of photo-electrons. Charge-gains in excess of 10 5 were obtained for gas mixtures containing percentages of quencher higher than 20% while photo-electron extraction efficiency achieved ∼ 50% for He/CF 4 and ∼ 30% for He/CH 4 . Single photon electron measurements were also performed to assess the maximal gains reached in this regime. A discussion for future GPM cryogenic applications is presented

Modification of the 137Cs, 90Sr, and 60Co transfer to wheat plantlets by NH4+ fertilizers.

Science.gov (United States)

Guillén, J; Muñoz-Muñoz, G; Baeza, A; Salas, A; Mocanu, N

2017-03-01

Inorganic fertilizers are used as agricultural countermeasures intended to inhibit the soil to plant transfer of radionuclides after a radioactive fallout. Two NH 4 + fertilizers, diammonium phosphate (DAP) and NPK, were applied to soil contaminated with a mixture of radionuclides to analyze whether they modify the transfer of 137 Cs, 90 Sr, and 60 Co and stable elements (K, Na, Ca, and Mg) to wheat plantlets grown under controlled laboratory conditions. DAP introduced NH 4 + in the soil, which can increase 137 Cs transfer, while NPK also introduced K + , which can decrease it. The application of DAP increased the accumulation of 137 Cs in wheat plantlets with increasing application rate, so did the 137 Cs/K in plantlets. Regarding the NPK application, the 137 Cs increased in all treatments, but at maximum rate, the available K introduced by the fertilizer was probably able to partially satisfy the nutritional requirements of the wheat plantlet and the 137 Cs decreased relative to the recommended rate. The 137 Cs/K ratio in plantlet decreased with increasing NPK rates. The transfer of 90 Sr increased with increasing DAP rate and only at the maximum NPK rate. The 60 Co transfer only increased at the maximum application rates for DAP and NPK. These modifications should be considered when using these fertilizers as agricultural countermeasures.

The application of image processing software: Photoshop in environmental design

Science.gov (United States)

Dong, Baohua; Zhang, Chunmi; Zhuo, Chen

2011-02-01

In the process of environmental design and creation, the design sketch holds a very important position in that it not only illuminates the design's idea and concept but also shows the design's visual effects to the client. In the field of environmental design, computer aided design has made significant improvement. Many types of specialized design software for environmental performance of the drawings and post artistic processing have been implemented. Additionally, with the use of this software, working efficiency has greatly increased and drawings have become more specific and more specialized. By analyzing the application of photoshop image processing software in environmental design and comparing and contrasting traditional hand drawing and drawing with modern technology, this essay will further explore the way for computer technology to play a bigger role in environmental design.

Electronic structure and optical properties of Cs2HgCl4: DFT calculations and X-ray photoelectron spectroscopy measurements

Science.gov (United States)

Lavrentyev, A. A.; Gabrelian, B. V.; Vu, V. T.; Parasyuk, O. V.; Fedorchuk, A. O.; Khyzhun, O. Y.

2016-10-01

A high-quality single crystal of cesium mercury tetrabromide, Cs2HgCl4, was synthesized by using the vertical Bridgman-Stockbarger method and its electronic structure was studied from both experimental and theoretical viewpoints. In particular, X-ray photoelectron spectra were measured for both pristine and Ar+ ion-bombarded Cs2HgCl4 single crystal surfaces. The present XPS measurements indicate that the Cs2HgCl4 single crystal surface is sensitive with respect to Ar+ ion-bombardment: such a treatment changes substantially its elemental stoichiometry. With the aim of exploring total and partial densities of states within the valence band and conduction band regions of the Cs2HgCl4 compound, band-structure calculations based on density functional theory (DFT) using the augmented plane wave + local orbitals (APW + lo) method as incorporated within the WIEN2k package are performed. The calculations indicate that the Cl 3p states are the principal contributors in the upper portion of the valence band, while the Hg 5d and Cs 5p states dominate in its lower portion. In addition, the calculations allow for concluding that the unoccupied Cl p and Hg s states are the main contributors to the bottom of the conduction band. Furthermore, main optical characteristics of Cs2HgCl4, namely dispersion of the absorption coefficient, real and imaginary parts of dielectric function, electron energy-loss spectrum, refractive index, extinction coefficient and optical reflectivity, are elucidated based on the DFT calculations.

Heat enhancement of radiation resistivity of evaporated CsI, KI and KBr photocathodes

CERN Document Server

Tremsin, A S

2000-01-01

The photoemissive stability of as-deposited and heat-treated CsI, KI and KBr evaporated thin films under UV radiation is examined in this paper. After the deposition, some photocathodes were annealed for several hours at 90 deg. C in vacuum and their performance was then compared to the performance of non-heated samples. We observed that the post-evaporation thermal treatment not only increases the photoyield of CsI and KI photocathodes in the spectral range of 115-190 nm, but also reduces CsI, KI and KBr photocurrent degradation that occurs after UV irradiation. KBr evaporated layers appeared to be more radiation-resistant than CsI and KI layers. Post-deposition heat treatment did not result in any significant variation of KBr UV sensitivity.

Radioecological studies of 137Cs in limnological ecosystems. Biochemical states of 137Cs accumulated in killifish (Medaka, Oryzias latipes) meat

International Nuclear Information System (INIS)

Miyake, Sadaaki; Motegi, Misako; Oosawa, Takashi; Nakazawa, Kiyoaki; Izumo, Yoshiro; Nakamura, Fumio.

1997-01-01

Biochemical states of 137 Cs accumulated in killifish's (Medaka, Oryzias latipes) meat were investigated in order to elucidate the accumulation mechanism of the radionuclide in goldfish, Carassius auratus auratus, examined in our preceding report. Most of 137 Cs radioactivity in the killifish's raw meat accumulated this radionuclide in the radioactive freshwater, were found in the non-protein nitrogenous compound (NPNC) fraction (>92%), also in the killifish's control raw meat mixed with 137 Cs, the difference between both meat samples was not clear. As the results of gel filtration profiles on Sephadex G-25 for the NPNC fraction of these meats, each only one radioactive peak was shown, also similar to 137 CsCl solution. Moreover, these peaks appeared at the same position. On the other hand, the peak positions absorbed at OD 280nm in the samples were different from those of each radioactive peak. It was so suggested that 137 Cs accumulated in the killifish's meat was shown not to be binding to protein's composition. Furthermore, as the results on thin-layer chromatography, ion-exchange resin chromatography and reaction with 137 Cs in samples and ammonium phosphomolybdate, 137 Cs in the NPNC fraction of the killifish's meat was not almost different from those of each control and 137 CsCl solution. (author)

CsPb2Br5 Single Crystals: Synthesis and Characterization

KAUST Repository

Dursun, Ibrahim

2017-08-02

CsPb2Br5 is a ternary halogen-plumbate material with close characteristics to well-reported halide perovskites. Due to its unconventional two-dimensional structure, CsPb2Br5 is being looked at broadly for potential applications in optoelectronics. CsPb2Br5 investigations are currently limited to nanostructures and powder forms of the material, which present unclear and conflicting optical properties. In this study, we present the synthesis and characterization of CsPb2Br5 bulk single crystals, which enabled us to finally clarify the material\\'s optical features. Our CsPb2Br5 crystal has a two-dimensional structure with Pb2Br5- layers spaced by Cs+ cations, and exhibits a ~3.1 eV indirect bandgap with no emission in the visible spectrum.

The application of parameters for comprehensive smile esthetics by digital smile design programs: A review of literature

Directory of Open Access Journals (Sweden)

Doya Omar

2018-01-01

Full Text Available Cosmetic dentistry is increasingly becoming an issue of concern to patients who hope to improve their smile. A systematic and comprehensive dentofacial analysis must be performed before commencing esthetic treatment. Several computer software programs have been developed for digital smile design (DSD to assist clinicians in this process. This article compares DSD programs commonly used in cosmetic dentistry and their ability to assess esthetic parameters. A literature review was performed of current dentofacial aesthetic parameters and clinical applications of computer technology to assess facial, dentogingival and dental esthetics. Eight DSD programs (Photoshop CS6, Keynote, Planmeca Romexis Smile Design, Cerec SW 4.2, Aesthetic Digital Smile Design, Smile Designer Pro, DSD App and VisagiSMile were compared. Photoshop, Keynote and Aesthetic Digital Smile Design included the largest number of esthetic analysis parameters. Other studied DSD programs presented deficiencies in their ability to analyze facial esthetic parameters but included comprehensive dentogingival and dental esthetic functions. The DSD App, Planmeca Romexis Smile Design, and Cerec SW 4.2 were able to perform 3D analysis; furthermore, Cerec SW 4.2 and PRSD could be used jointly with CAD/CAM. The DSD App and Smile Designer Pro are available as mobile phone applications. It can be concluded that despite the fact that they were not specifically designed for dental diagnosis, Photoshop CS6 and Keynote provide a more comprehensive smile analysis than most specialized DSD programs. However, other program functions should also be considered when deciding which DSD program is applicable to individual clinical setups.

Transfer of 137Cs from soil to plants in a wet montane forest in subtropical Taiwan

International Nuclear Information System (INIS)

Chih-Yu Chiu

1999-01-01

The distribution of 137 Cs in an undisturbed, multistoried, subtropical wet montane forest ecosystem surrounding Yuanyang Lake (lake surface level ca. 1670 m, in northeastern Taiwan), was investigated. The mossy forest here represents a currently-rare perhumid temperate environment in subtropical region. The radioactivity concentration of 137 Cs was determined by γ-spectroscopy with a Ge(Li) detector. Although the soil is extremely acidic (pH 3.3 to 3.6) and the rainfall is high, 137 Cs is evidently retained in the organic layer. The radioactivity concentration of 137 Cs in surface soil ranges from 28 to 71 Bq x kg -1 . The concentrations of 137 Cs in the ground moss layer and litter were much lower than that in the soil organic layer; this suggests that 137 Cs detected is not from the newly deposited radioactive fallout. The radioactivity concentration and transfer factor (TF) of 137 Cs varied with plant species. Shrubs and ferns have higher values than a coniferous tree (Taiwan cedar). The TF in this ecosystem is as high as 0.21 to 1.88. The high values of TF is attributed to the abundance of the organic matter in the forest soils. The rapid recycling of 137 Cs through the soil-plant system of this undisturbed multistoried ecosystem suggests the existence of an internal cycling that help the accumulation of 137 Cs in this ecosystem. (author)

Residence half-time of {sup 137}Cs in the top-soils of Japanese paddy and upland fields

Energy Technology Data Exchange (ETDEWEB)

Komamura, Misako [National Inst. of Agro-Environmental Sciences, Tsukuba, Ibaraki (Japan); Tsumura, Akito; Kodaira, Kiyoshi

1999-03-01

A series of top-soil samples of 14 paddy fields and 10 upland fields in Japan, were annually collected during more than 30 years, to be examined in the contents of {sup 137}Cs. The data, which were obtained by the use of a gamma spectrometric system, received some statistical treatments to distinguish the annual decline of {sup 137}Cs contents from deviations. Then the authors calculated `residence half-time of {sup 137}Cs` within top-soil, and `eluviation rate of {sup 137}Cs` from top to the sub-layer of the soil. The following nationwide results were obtained irrespective of paddy or upland field: (1) The `apparent residence half-time` was estimated as 16 - 17 years. This consists of both effects of eluviation and nuclear disintegration. (2) The true residence half-time` was reported as 41 - 42 years. This depends on the eluviation speed of {sup 137}Cs exclusively, because the influence of nuclear disintegration has been compensated. (3) The eluviation rate of {sup 137}Cs from top-soil down to the sub-soil was 1.6 - 1.7% per year. (4) The ratio of distribution of {sup 137}Cs between top-soil and the sub-soil was estimated to be 6:4 as average at the date of 1996. (author)

Chronological study of 137Cs input to the Black Sea deep and shelf sediments

International Nuclear Information System (INIS)

Gulin, S.B.; Polikarpov, G.G.; Egorov, V.N.; Aarkrog, A.; Nielsen, S.P.

1997-01-01

The chart of the post-Chernobyl 137 Cs distribution in the upper Black Sea sediments was made. The field of sediments with the highest 137 Cs activity was found near the Danube River mouth. The age of sediment layers as well as the sedimentation rates were calculated from 137 Cs vertical profiles in the top of the uncompacted sediments nearby the Danube (11.5 mm yr -1 ), the NW Black Sea slope (2.2 mm yr -1 ) and the deepest western area (0.4 mm yr -1 ). Subsequent assessments showed the high distinction of 137 Cs sedimentary fluxes and inventories between these sites related to different contributions of terrigenous matter in the sediments, as traced by 40 K. The results allow to reconstruct chronology of 137 Cs input to the Black Sea over the last decades. The traced three most notable phases correspond well with the periods of active nuclear weapon testings in the 1950's and 1960's as well as of the Chernobyl NPP accident. The post-Chernobyl dynamics of 137 Cs activity in the near Danube sediments traced from its dated profile was like that observed during the annual monitoring. (author)

A novel vanadosilicate with hexadeca-coordinated Cs+ ions as a highly effective Cs+ remover

International Nuclear Information System (INIS)

Datta, Shuvo Jit; Moon, Won Kyung; Choi, Do Young; Hwang, In Chul; Yoon, Kyung Byung

2014-01-01

The effective removal of 137 Cs + ions from contaminated groundwater and seawater and from radioactive nuclear waste solutions is crucial for public health and for the continuous operation of nuclear power plants. Various 137 Cs + removers have been developed, but more effective 137 Cs + removers are still needed. A novel microporous vanadosilicate with mixed-valence vanadium (V 4+ and V 5+ ) ions is now reported, which shows an excellent ability for Cs + capture and immobilization from groundwater, seawater, and nuclear waste solutions. This material is superior to other known materials in terms of selectivity, capacity, and kinetics, and at very low Cs + concentrations, it was found to be the most effective material for the removal of radioactive Cs + ions under the test conditions. This novel vanadosilicate also contains hexadeca-coordinated Cs + ions, which corresponds to the highest coordination number ever described.

Determination of 137Cs activities in soil samples from east and south Marmara region, Turkey

International Nuclear Information System (INIS)

Kilic, Oe.; Belivermis, M.; Cotuk, Y.; Coskun, M.; Cayir, A.; Kuecer, R.

2006-01-01

Activity concentrations of 1 37Cs, 4 0K and physico-chemical parameters of soil samples collected from 99 sampling stations in the east and south of Marmara Region of Turkey were determined. The study region was divided into 20 x 20 km grids and soil samples collected randomly in each square from 0-5 cm surface layer. Activities were measured by means of multichannel gamma analyser provided with high purity germanium detector. Relations among 1 37Cs concentrations and physico-chemical parameters of soils and climatic factors of the region were evaluated. Arc View GIS version 3.1 was used mapping of study area. Distribution of radionuclide concentrations in the region illustrated with contour maps using Surfer 8.0 for Windows. The range of activity concentrations of 1 37Cs and 4 0K were measured to be 0.92-153.72 and 69.24-1085.57 Bq/kg respectively

Ion exchange of alkaline metals on the thin-layer zinc ferrocyanide

International Nuclear Information System (INIS)

Betenekov, N.D.; Buklanov, G.V.; Ipatova, E.G.; Korotkin, Yu.S.

1991-01-01

Basic regularities of interphase distribution in the system of thin-layer sorbent on the basis of mixed zinc ferrocyanide (FZ)-alkaline metal solution (Na, K, Rb, Cs, Fr) in the column chromatography made are studied. It is established that interphase distribution of microgram amounts of alkaline metals in the systems thin-layer FZ-NH 4 NO 3 electrolyte solutions is of ion-exchange character and subjected to of law effective mass. It is shown that FZ thin-layer material is applicable for effective chromatographic separation of alkaline metal trace amounts. An approach to the choice of a conditions of separate elution of Na, K, Rb, Cs, Fr in the column chromatography mode

[Perception of asymmetry smile: Attempt to evaluation through Photoshop].

Science.gov (United States)

Diakite, C; Diep, D; Labbe, D

2016-04-01

In the labial palliative surgery of facial paralysis, it can persist asymmetry smile. Evaluate the impact of an augmentation or reduction of the commissural course on the perception of a smile anomaly, and determine from which asymmetry threshold, the smile is estimated unsightly. We took a picture of two people with a smile not forced; including one with a "cuspid smile", and the another one with a "Mona Lisa" smile. The pictures obtained were modified by the Photoshop software, to simulate an asymmetry labial smile. The changes were related to the move of the left labial commissure, the left nasolabial furrow, and the left cheek using under-correction and overcorrection, every 4 mm. Three pictures with under-correction and four pictures with over-correction were obtained. These smiles were shown to three groups of five people, which included doctors in smile specialties, doctors in other specialties, and non-doctors. Participants were then asked to indicate on which of the pictures, the smile seemed abnormal. Between -8 mm under-correction, and +8 mm over-correction, the asymmetry of the commissural course does not hinder the perception of smile. In the labial palliative surgery of facial paralysis, in the case of persistent asymmetry, there is a tolerance in the perception of "normality" of smile concerning the amplitude of the commissural course going up to 8 mm of asymmetric with under-correction or over-correction. Copyright © 2015 Elsevier Masson SAS. All rights reserved.

Modular metal chalcogenide chemistry: secondary building blocks as a basis of the silicate-type framework structure of CsLiU(PS_4)_2

International Nuclear Information System (INIS)

Neuhausen, Christine; Rocker, Frank; Tremel, Wolfgang

2012-01-01

The novel uranium thiophosphate CsLiU(PS_4)_2 has been synthesized by reacting uranium metal, Cs_2S, Li_2S, S, and P_2S_5 at 700 C in an evacuated silica tube. The crystal structure was determined by single-crystal X-ray diffraction techniques. CsLiU(PS_4)_2 crystallizes in the rhombohedral space group R anti 3c (a = 15.2797(7) Aa; c = 28.778(2) Aa, V = 5818.7(5) Aa"3, Z = 18). The structure of CsLiU(PS_4)_2 is a unique three-dimensional U(PS_4)_2"2"- framework with large tunnels with an approximate diameter of 6.6 Aa running parallel to the crystallographic c axis. The tunnels are filled with Cs"+ cations. The smaller Li"+ cations are located at tetrahedral sites at the periphery of the channels. In the structure of CsLiU(PS_4)_2 the uranium atoms are coordinated by thiophosphate groups in a pseudotetrahedral fashion, and the PS_4 groups act as linear connectors. Topologically, CsLiU(PS_4)_2 may be regarded a chalcogenide analogue of silicate frameworks, with the uranium atoms and PS_4 groups replacing silicon and oxygen atoms. Alternatively, CsLiU(PS_4)_2 may be viewed as a coordination polymer, which is formed in salt melts by the solid state equivalent of the ''self-assembly'' reactions in solution. Magnetic susceptibility measurements indicated Curie-Weiss-type behavior between 4 K and 300 K. The μ_e_f_f of 2.83 μ_B at 300 K is in agreement with an f"2 configuration of U"4"+. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Using Photoshop with images created by a confocal system.

Science.gov (United States)

Sedgewick, Jerry

2014-01-01

Many pure colors and grayscales tones that result from confocal imaging are not reproducible to output devices, such as printing presses, laptop projectors, and laser jet printers. Part of the difficulty in predicting the colors and tones that will reproduce lies in both the computer display, and in the display of unreproducible colors chosen for fluorophores. The use of a grayscale display for confocal channels and a LUT display to show saturated (clipped) tonal values aids visualization in the former instance and image integrity in the latter. Computer monitors used for post-processing in order to conform the image to the output device can be placed in darkened rooms, and the gamma for the display can be set to create darker shadow regions, and to control the display of color. These conditions aid in visualization of images so that blacks are set to grayer values that are more amenable to faithful reproduction. Preferences can be set in Photoshop for consistent display of colors, along with other settings to optimize use of memory. The Info window is opened so that tonal information can be shown via readouts. Images that are saved as indexed color are converted to grayscale or RGB Color, 16-bit is converted to 8-bit when desired, and colorized images from confocal software is returned to grayscale and re-colorized according to presented methods so that reproducible colors are made. Images may also be sharpened and noise may be reduced, or more than one image layered to show colocalization according to specific methods. Images are then converted to CMYK (Cyan, Magenta, Yellow and Black) for consequent assignment of pigment percentages for printing presses. Changes to single images and multiple images from image stacks are automated for efficient and consistent image processing changes. Some additional changes are done to those images destined for 3D visualization to better separate regions of interest from background. Files are returned to image stacks, saved and

Theoretical study for heterojunction surface of NEA GaN photocathode dispensed with Cs activation

Science.gov (United States)

Xia, Sihao; Liu, Lei; Wang, Honggang; Wang, Meishan; Kong, Yike

2016-09-01

For the disadvantages of conventional negative electron affinity (NEA) GaN photocathodes activated by Cs or Cs/O, new-type NEA GaN photocathodes with heterojunction surface dispensed with Cs activation are investigated based on first-principle study with density functional theory. Through the growth of an ultrathin n-type GaN cap layer on p-type GaN emission layer, a p-n heterojunction is formed on the surface. According to the calculation results, it is found that Si atoms tend to replace Ga atoms to result in an n-type doped cap layer which contributes to the decreasing of work function. After the growth of n-type GaN cap layer, the atom structure near the p-type emission layer is changed while that away from the surface has no obvious variations. By analyzing the E-Mulliken charge distribution of emission surface with and without cap layer, it is found that the positive charge of Ga and Mg atoms in the emission layer decrease caused by the cap layer, while the negative charge of N atom increases. The conduction band moves downwards after the growth of cap layer. Si atom produces donor levels around the valence band maximum. The absorption coefficient of GaN emission layer decreases and the reflectivity increases caused by n-type GaN cap layer.

Uptake and distributions of 90Sr and 137Cs in rice plants

International Nuclear Information System (INIS)

Tsukada, Hirofumi; Takeda, Akira; Hasegawa, Hidenao

2008-01-01

Polished rice is a staple food in Asian countries and ingestion of polished rice is one of the most important pathways of radionuclides into humans. Inedible parts of rice plants are returned to the soil as fertilizer and are used as an ingredient of feed for livestock. Strontium-90 and 137 Cs are important radionuclides for the assessment of radiation exposure to the public because of their high fission yield, long-half lives and transferability in the environment. The purpose of the present study is to obtain information on the distributions of 90 Sr and 137 Cs in rice plant components for better understanding of the fate of the radionuclides in an agricultural environment. Rice plants were cultivated in an experimental field and collected at harvest time. The concentrations of 90 Sr and 137 Cs in the soil were 5.6 and 4.4 Bq kg -1 , respectively. Rice plant samples were separated into polished rice, rice bran, hull, straw and root parts, and then the concentrations of 90 Sr and 137 Cs in the samples were determined. The concentrations of 90 Sr and 137 Cs in polished rice were 0.012 and 0.0048 Bq kg -1 dry weight, respectively. The concentrations of 90 Sr and 137 Cs varied by two and one orders of magnitudes in rice plant components, respectively. The edible component, polished rice, accounted for 32% of the total dry weight. In the entire rice plants, only 0.5% of the total 90 Sr and 10% of the total 137 Cs were found in polished rice. Contents of 90 Sr and 137 Cs in the above ground parts were 0.84 and 0.021 Bq m -2 , respectively. For each cropping, the percentages of 90 Sr and 137 Cs uptake from the upper soil layer to the aboveground biomass of rice plants were calculated as 0.094 and 0.0030% of their soil inventories, respectively. (author)

The fate of long - lived radionuclides 137Cs and 90Sr in the Black Sea after Chernobyl NPP accident: results of twenty - year observations

International Nuclear Information System (INIS)

Stokozov, N. A.; Egorov, V. N.; Polikarpov, G. G.; Mirzoeva, N. Y.; Gulin, S. B.

2006-01-01

The presentation summarizes studies of 1 37Cs and 9 0Sr pollution of the Black Sea Basin carried out by Institute of Biology of the Southern Seas during 1986-2005 following the Chernobyl NPP accident. Its goal was to assess inflows of 1 37Cs and 9 0Sr from the Dnieper and the Danube Rivers, outflow through the Bosphorus Strait, inventories in bottom sediments and temporary evolution of 1 37Cs and 9 0Sr inventories in the Black Sea water column. Besides, the temporary evolution of 1 37Cs and 9 0Sr profiles in the Black Sea deep-water basin was used to estimations of a large-scale vertical water mixing. It has been estimated that the atmospheric fall outs during the first days of May 1986 have deposited 1.7-2.4 PBq of 1 37Cs on the Black Sea surface (nearly 2% of total 1 37Cs release in the environment). Therefore, 1 37Cs inventory in the 0-50 m layer have increased by a factor of 6-10 and the total 1 37Cs inventory in the whole basin have increased at least by a factor of 2 in comparison with the pre-Chernobyl value - 1.4+/-0.3 PBq. 1 37Cs input from the Danube and the Dnieper Rivers was insignificant in comparison with short-term atmospheric fall outs. The results of observations and mathematical modelling are testified that in the surface layers 0-50 and 0-200 m of the Black Sea deep-water basin in 1986-2000 an exponential decreases of the 1 37Cs inventories with an effective half-lifes of 5-6 years and 9-13 years, respectively, have been observed. The process of vertical water mixing has been observed mainly in the 0-200 m layer. The contribution of Chernobyl-origin 9 0Sr from atmospheric fallout was estimated around in 0.1-0.3 PBq. Pre-accident 9 0Sr level nearly 20 Bq m - 3 was reached by 1988. At the same time, an active input of 9 0Sr from the Dnieper and Danube Rivers has been observed. The total amount of 9 0Sr delivered by the two rivers into the Black Sea was estimated to be nearly 0.1 PBq in the 1986-1995. Under conditions of insignificant river input

Crystal structure relation between tetragonal and orthorhombic CsAlD{sub 4}: DFT and time-of-flight neutron powder diffraction studies

Energy Technology Data Exchange (ETDEWEB)

Bernert, Thomas; Krech, Daniel; Felderhoff, Michael; Weidenthaler, Claudia [Department of Heterogeneous Catalysis, Max-Planck-Institut fuer Kohlenforschung, Muelheim/Ruhr (Germany); Kockelmann, Winfried [Rutherford Appleton Laboratory, Harwell Oxford, Didcot (United Kingdom); Frankcombe, Terry J. [Research School of Chemistry, The Australian National University, Canberra, ACT (Australia); School of Physical, Environmental and Mathematic Sciences, The University of New South Wales, Canberra, ACT (Australia)

2015-11-15

The crystal structures of orthorhombic and tetragonal CsAlD{sub 4} were refined from time-of-flight neutron powder diffraction data starting from atomic positions predicted from DFT calculations. The earlier proposed crystal structure of orthorhombic CsAlH{sub 4} is confirmed. For tetragonal CsAlH{sub 4}, DFT calculations predicted a crystal structure in I4{sub 1}/amd as potential minimum structure, while from neutron diffraction studies of CsAlD{sub 4} best refinement is obtained for a disordered structure in the space group I4{sub 1}/a, with a = 5.67231(9) Aa, c = 14.2823(5) Aa. While the caesium atoms are located on the Wyckoff position 4b and aluminium at Wyckoff position 4a, there are two distinct deuterium positions at the Wyckoff position 16f with occupancies of 50 % each. From this structure, the previously reported phase transition between the orthorhombic and tetragonal polymorphs could be explained. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

New sulfido antimonates of the heavy alkali metals. Synthesis, crystal structure and chemical bonding of (K/Rb/Cs){sub 3}SbS{sub 3} and Cs{sub 3}SbS{sub 4} . H{sub 2}O; Neue Sulfido-Antimonate der schweren Alkalimetalle. Synthese, Kristallstruktur und chemische Bindung von (K/Rb/Cs){sub 3}SbS{sub 3} und Cs{sub 3}SbS{sub 4} . H{sub 2}O

Energy Technology Data Exchange (ETDEWEB)

Schindler, Lisa V.; Schwarz, Michael; Roehr, Caroline [Freiburg Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

2013-12-15

The new sulfido antimonates(III) (Rb/Cs){sub 3}SbS{sub 3} were prepared from the alkali metal sulfides Rb{sub 2}S/Cs{sub 2}S{sub 2} and elemental antimony and sulfur or Sb{sub 2}S{sub 3} at reaction temperatures of about 700 C. The known isotypic potassium compound was similarly synthesized from the elements. The structures of the light-yellow crystals were refined using single-crystal X-ray data. Both compounds are isotypic to the respective Na salt forming the Na{sub 3}AsS{sub 3} structure type (cubic, space group P2{sub 1}3, K/Rb/Cs: a = 947.21(7)/982.28(5)/1025.92(5) pm, Z = 4, R1 = 0.0159/0.0560/0.0582). The {psi}-tetrahedral SbS{sub 3}{sup 3-} anions with Sb-S bond lengths of 242 pm are arranged in a cubic face centered packing, in which the three crystallographically different A{sup +} cations occupy the tetrahedral and octahedral voids, overall exhibiting a distorted octahedral sulfur coordination. The chemical bonding and the characteristics of the stereochemically active lone electron pair have been investigated by means of FP-LAPW band structure calculations. Needle-shaped crystals of the monohydrate of the antimony(V) salt Cs{sub 3}SbS{sub 4} . H{sub 2}O were obtained from a suspension of Sb{sub 2}O{sub 3}, CsOH and elemental sulfur. Cs{sub 3}SbS{sub 4} . H{sub 2}O crystallizes in a new structure type (monoclinic, space group P2{sub 1}/c, a = 987.17(10), b = 994.83(7), c = 1600.46(14) pm, {beta} = 126.895(8) , Z = 4, R1 = 0.0234). As expected, the Sb-S distances (233.1-234.7 pm) in the nearly ideally tetrahedral anion SbS{sub 4}{sup 3-} are considerably shorter than in the antimonates(III) but match the bond lengths in the anhydrous sulfido antimonate(V) Cs{sub 3}SbS{sub 4}. Due to their similar fcc-like anion packing and the stereochemically active lone electron pair of Sb in the antimonates(III), the whole series of compounds A{sub 3}Sb{sup III,V}S{sub 3/4} shows a uniform structure relation, which is elucidated using crystallographic group

Improving CS regulations.

Energy Technology Data Exchange (ETDEWEB)

Nesse, R.J.; Scheer, R.M.; Marasco, A.L.; Furey, R.

1980-10-01

President Carter issued Executive Order 12044 (3/28/78) that required all Federal agencies to distinguish between significant and insignificant regulations, and to determine whether a regulation will result in major impacts. This study gathered information on the impact of the order and the guidelines on the Office of Conservation and Solar Energy (CS) regulatory practices, investigated problems encountered by the CS staff when implementing the order and guidelines, and recommended solutions to resolve these problems. Major tasks accomplished and discussed are: (1) legislation, Executive Orders, and DOE Memoranda concerning Federal administrative procedures relevant to the development and analysis of regulations within CS reviewed; (2) relevant DOE Orders and Memoranda analyzed and key DOE and CS staff interviewed in order to accurately describe the current CS regulatory process; (3) DOE staff from the Office of the General Counsel, the Office of Policy and Evaluation, the Office of the Environment, and the Office of the Secretary interviewed to explore issues and problems encountered with current CS regulatory practices; (4) the regulatory processes at five other Federal agencies reviewed in order to see how other agencies have approached the regulatory process, dealt with specific regulatory problems, and responded to the Executive Order; and (5) based on the results of the preceding four tasks, recommendations for potential solutions to the CS regulatory problems developed. (MCW)

Ultrasound estimates of muscle quality in older adults: reliability and comparison of Photoshop and ImageJ for the grayscale analysis of muscle echogenicity.

Science.gov (United States)

Harris-Love, Michael O; Seamon, Bryant A; Teixeira, Carla; Ismail, Catheeja

2016-01-01

Background. Quantitative diagnostic ultrasound imaging has been proposed as a method of estimating muscle quality using measures of echogenicity. The Rectangular Marquee Tool (RMT) and the Free Hand Tool (FHT) are two types of editing features used in Photoshop and ImageJ for determining a region of interest (ROI) within an ultrasound image. The primary objective of this study is to determine the intrarater and interrater reliability of Photoshop and ImageJ for the estimate of muscle tissue echogenicity in older adults via grayscale histogram analysis. The secondary objective is to compare the mean grayscale values obtained using both the RMT and FHT methods across both image analysis platforms. Methods. This cross-sectional observational study features 18 community-dwelling men (age = 61.5 ± 2.32 years). Longitudinal views of the rectus femoris were captured using B-mode ultrasound. The ROI for each scan was selected by 2 examiners using the RMT and FHT methods from each software program. Their reliability is assessed using intraclass correlation coefficients (ICCs) and the standard error of the measurement (SEM). Measurement agreement for these values is depicted using Bland-Altman plots. A paired t-test is used to determine mean differences in echogenicity expressed as grayscale values using the RMT and FHT methods to select the post-image acquisition ROI. The degree of association among ROI selection methods and image analysis platforms is analyzed using the coefficient of determination (R (2)). Results. The raters demonstrated excellent intrarater and interrater reliability using the RMT and FHT methods across both platforms (lower bound 95% CI ICC = .97-.99, p Photoshop was .97 and 1.05 grayscale levels when using the RMT and FHT ROI selection methods, respectively. Comparatively, the SEM values were .72 and .81 grayscale levels, respectively, when using the RMT and FHT ROI selection methods in ImageJ. Uniform coefficients of determination (R (2) = .96

Electric conductivity of solid solutions the Cs3-2xMxPO4 (M=Ba, Sr, Ca, Mg) systems

International Nuclear Information System (INIS)

Burmakin, E.I.; Stroev, S.S.; Shekhtman, G.Sh.; Antonov, B.D.

2003-01-01

The solid solutions in the Cs 3-2x M x PO 4 (M=Ba, Sr, Ca, Mg) system are synthesized and their thermal behavior and electric conductivity are studied. The introduction of the alkaline earth metal cations into cesium orthophosphates is accompanied by the shift of the phase transition occurring in the pure Cs 3 PO 4 at 450-620 Deg C into the low-temperature area as well as by increase in the cesium-cation conductivity at low temperatures. The electric conductivity in the area of existence of the Cs 3 PO 4 high-temperature modification slightly depends on the availability and concentration of the modifying additions, which make it possible to suppose the calcium sublattice structural disordering [ru

Inside Perovskites: Quantum Luminescence from Bulk Cs4PbBr6 Single Crystals

KAUST Repository

de Bastiani, Michele; Dursun, Ibrahim; Zhang, Yuhai; Alshankiti, Buthainah; Miao, Xiaohe; Yin, Jun; Yengel, Emre; Alarousu, Erkki; Turedi, Bekir; Almutlaq, Jawaher; Saidaminov, Makhsud I.; Mitra, Somak; Gereige, Issam; Alsaggaf, Ahmed; Zhu, Yihan; Han, Yu; Roqan, Iman S.; Bredas, Jean-Luc; Mohammed, Omar F.; Bakr, Osman

2017-01-01

the chemistry and structure of these materials, without revealing the origins of their optical behaviour, which is contradictory to the well-studied APbX3 perovskites. In this work, we synthesize single crystals of Cs4PbBr6 0D-PRS, and investigated the origins

CS Informativeness Governs CS-US Associability

Science.gov (United States)

Ward, Ryan D.; Gallistel, C. R.; Jensen, Greg; Richards, Vanessa L.; Fairhurst, Stephen; Balsam, Peter D

2012-01-01

In a conditioning protocol, the onset of the conditioned stimulus (CS) provides information about when to expect reinforcement (the US). There are two sources of information from the CS in a delay conditioning paradigm in which the CS-US interval is fixed. The first depends on the informativeness, the degree to which CS onset reduces the average expected time to onset of the next US. The second depends only on how precisely a subject can represent a fixed-duration interval (the temporal Weber fraction). In three experiments with mice, we tested the differential impact of these two sources of information on rate of acquisition of conditioned responding (CS-US associability). In Experiment 1, we show that associability (the inverse of trials to acquisition) increases in proportion to informativeness. In Experiment 2, we show that fixing the duration of the US-US interval or the CS-US interval or both has no effect on associability. In Experiment 3, we equated the increase in information produced by varying the C̅/T̅ ratio with the increase produced by fixing the duration of the CS-US interval. Associability increased with increased informativeness, but, as in Experiment 2, fixing the CS-US duration had no effect on associability. These results are consistent with the view that CS-US associability depends on the increased rate of reward signaled by CS onset. The results also provide further evidence that conditioned responding is temporally controlled when it emerges. PMID:22468633

137Cs vertical migration in a deciduous forest soil following the Fukushima Dai-ichi Nuclear Power Plant accident

International Nuclear Information System (INIS)

Nakanishi, Takahiro; Matsunaga, Takeshi; Koarashi, Jun; Atarashi-Andoh, Mariko

2014-01-01

The large amount of 137 Cs deposited on the forest floor because of the Fukushima Dai-ichi Nuclear Power Plant accident represents a major potential long-term source for mobile 137 Cs. To investigate 137 Cs mobility in forest soils, we investigated the vertical migration of 137 Cs through seepage water, using a lysimetric method. The study was conducted in a deciduous forest soil over a period spanning 2 month to 2 y after the Fukushima nuclear accident. Our observations demonstrated that the major part of 137 Cs in the litter layer moved into the mineral soil within one year after the accident. On the other hand, the topsoil prevented migration of 137 Cs, and only 2% of 137 Cs in the leachate from litter and humus layer penetrated below a 10 cm depth. The annual migration below a 10 cm depth accounted for 0.1% of the total 137 Cs inventory. Therefore, the migration of 137 Cs by seepage water comprised only a very small part of the total 137 Cs inventory in the mineral soil, which was undetectable from the vertical distribution of 137 Cs in the soil profile. In the present and immediate future, most of the 137 Cs deposited on the forest floor will probably remain in the topsoil successively, although a small but certain amount of bioavailable 137 Cs exists in forest surface soil. -- Highlights: • Lysimeter captured 137 Cs mobility in a forest soil after the Fukushima accident. • Major part of 137 Cs in the litter layer moved into the mineral soil within a year. • Litter-leachate 137 Cs was predominantly adsorbed within the topsoil. • The annual migration below a 10 cm depth was 0.1% of the total 137 Cs inventory

Luminescence and scintillation properties of Ce-doped Cs2ZnCl4 crystals

Science.gov (United States)

Sugawara, K.; Koshimizu, M.; Yanagida, T.; Fujimoto, Y.; Haruki, R.; Nishikido, F.; Kishimoto, S.; Asai, K.

2015-03-01

In this study, we have synthesized scintillation materials based on Ce-doped Cs2ZnCl4 crystals. The light yield was enhanced by up to 20% by doping Cs2ZnCl4 with Ce3+ ions. In the scintillation time profiles, fast components exhibited decay time constants on the order of nanoseconds, which was ascribed to Auger-free luminescence (AFL). The light yield of the AFL component decreased at 10 mol% Ce3+ concentration, which is mainly attributed to the reabsorption of AFL photons inside the crystals by Ce3+ ions, as seen in the scintillation spectra. Long components had decay time constants of approximately 30 ns. In addition, at 10 mol% Ce3+ concentration, a prominent band appeared at approximately 500 nm in the scintillation spectrum, which was not observed in the photoluminescence spectra. The long components in the scintillation time profiles and the 500 nm band in the scintillation spectra were tentatively attributed to self-trapped excitons perturbed by Ce3+ ions.

Comparison of the depth distribution processes for 137Cs and 210Pbex in cultivated soils

International Nuclear Information System (INIS)

Zhang Yunqi; Zhang Xinbao; Long Yi; He Xiubin; Yu Xingxiu

2012-01-01

This paper focuses on the different processes of 137 Cs and 210 Pb ex depth distribution in cultivated soils. In view of their different fallout deposition processes, considering radionuclide will diffuse from the plough layer to the plough pan layer duo to the concentration gradient between the two layers, the 137 Cs and 210 Pb ex depth distribution processes were theoretically derived. Additionally, the theoretical derivation was verified by the measured 137 Cs and 210 Pb ex values in the soil core collected from wheat field in Fujianzhuang, Shanxi Province, China, and the 137 Cs and 210 Pb ex concentrations variation with depth in soils of the wheat field was explained rationally. The 137 Cs depth distribution state in cultivated soils will consistently vary with time due to 137 Cs continual decay and diffusion as an artificial radionuclide without sustainable fallout input since 1960s. In contrast, the 210 Pb ex depth distribution in cultivated soils will achieve steady state because of sustainable deposition of the naturally occurring 210 Pb ex fallout, and it can be concluded that the differences between the theoretical and the measured values, especially for 210 Pb ex , might be associated with the history of plough depth variation or LUCC. (authors)

A Raman spectroscopic study of the structural aspects of K2MgCl4 and Cs2MgCl4 as solid single crystals and molten salts

International Nuclear Information System (INIS)

Brooker, M.H.

1975-01-01

Polarized Raman spectra have been obtained for oriented single crystals of K 2 MgCl 4 and Cs 2 MgCl 4 at 77 and 298 K. The data are in excellent agreement with factor group analyses based on the space groups I 4 /mmm (D 17 4 /subh/) and Pnma (D 16 2 /subh/) for the K 2 MgCl 4 and Cs 2 MgCl 4 crystals. In K 2 MgCl 4 the magnesium is surrounded by six chloride ions in a distorted octahedral arrangement with a network structure such that neighboring octahedra share corners. In Cs 2 MgCl 4 a discrete tetrahedral MgCl 4 2- species is present. The 35 Cl-- 37 Cl isotopic splitting of the symmetric stetching mode of the tetrahedral MgCl 4 2- species has been resolved at 77 K and is similar to that observed for CCl 4 . Raman spectra for the high temperature solids and molten salts suggest that the coordination number of magnesium changes from six in solid K 2 MgCl 4 to four in the melt, whereas Cs 2 MgCl 4 melts with retention of the MgCl 4 2- tetrahedral complex. Additional evidence is presented to support previous reports that the MgCl 4 2- tetrahedral species is the principal complex ion in the melts, although a fraction of the magnesium appears to be present in a polynuclear complex, perhaps Mg 2 Cl 6 2-

Distribution of 137Cs in the Surface Soil of Serpong Nuclear Site

OpenAIRE

Lubis, E

2011-01-01

The distribution of 137Cs in the surface soil layer of Serpong Nuclear Site (SNS) was investigated by field sampling. The Objectives of the investigation is finding the profile of 137Cs distribution in the surface soil and the Tf value that can be used for estimation of radiation dose from livestock product-man pathways. The results indicates that the 137Cs activity in surface soil of SNS is 0.80 ± 0,29 Bq/kg, much lower than in the Antarctic. The contribution value of 137Cs from the operatio...

A study on H{sub 2}S permeability of CsHSO{sub 4} membranes

Energy Technology Data Exchange (ETDEWEB)

Mbah, Jonathan; Wolan, John T. [Department of Chemical and Biomedical Engineering, College of Engineering, University of South Florida, Tampa, FL 33620 (United States); Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL 33617 (United States); Krakow, Burton [Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL 33617 (United States); Stefanakos, Elias [Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL 33617 (United States); Department of Electrical Engineering, College of Engineering, University of South Florida, Tampa, FL 33617 (United States)

2009-03-15

The gas permeability of H{sub 2}S gas at 150 C through ultra-thin cesium hydrogen sulfate (CsHSO{sub 4}) membranes has been investigated. Gas chromatography-mass spectrometry analyses indicate that CsHSO{sub 4} membrane is impermeable to H{sub 2}S gas under test conditions. The apparent micropore diameter of the membrane averaged between 9.5 and 11.5 Aa with a maximum permeance of 0.09 Barrer (6.75 x 10{sup -19} m{sup 2} s{sup -1} Pa{sup -1}). Atomic force microscope and X-ray diffraction analyses show respectively that the surface morphology and crystal structure of the membranes are preserved, with no adverse effect from prolonged exposure to H{sub 2}S gas. Electrochemical impedance spectroscopy analysis confirm over a 30% decrease in membrane resistance via an 80% reduction in membrane thickness. (author)

Water-resistant, monodispersed and stably luminescent CsPbBr3/CsPb2Br5 core-shell-like structure lead halide perovskite nanocrystals

Science.gov (United States)

Qiao, Bo; Song, Pengjie; Cao, Jingyue; Zhao, Suling; Shen, Zhaohui; Gao, Di; Liang, Zhiqin; Xu, Zheng; Song, Dandan; Xu, Xurong

2017-11-01

Lead halide perovskite materials are thriving in optoelectronic applications due to their excellent properties, while their instability due to the fact that they are easily hydrolyzed is still a bottleneck for their potential application. In this work, water-resistant, monodispersed and stably luminescent cesium lead bromine perovskite nanocrystals coated with CsPb2Br5 were obtained using a modified non-stoichiometric solution-phase method. CsPb2Br5 2D layers were coated on the surface of CsPbBr3 nanocrystals and formed a core-shell-like structure in the synthetic processes. The stability of the luminescence of the CsPbBr3 nanocrystals in water and ethanol atmosphere was greatly enhanced by the photoluminescence-inactive CsPb2Br5 coating with a wide bandgap. The water-stable enhanced nanocrystals are suitable for long-term stable optoelectronic applications in the atmosphere.

Semi-automated relative quantification of cell culture contamination with mycoplasma by Photoshop-based image analysis on immunofluorescence preparations.

Science.gov (United States)

Kumar, Ashok; Yerneni, Lakshmana K

2009-01-01

Mycoplasma contamination in cell culture is a serious setback for the cell-culturist. The experiments undertaken using contaminated cell cultures are known to yield unreliable or false results due to various morphological, biochemical and genetic effects. Earlier surveys revealed incidences of mycoplasma contamination in cell cultures to range from 15 to 80%. Out of a vast array of methods for detecting mycoplasma in cell culture, the cytological methods directly demonstrate the contaminating organism present in association with the cultured cells. In this investigation, we report the adoption of a cytological immunofluorescence assay (IFA), in an attempt to obtain a semi-automated relative quantification of contamination by employing the user-friendly Photoshop-based image analysis. The study performed on 77 cell cultures randomly collected from various laboratories revealed mycoplasma contamination in 18 cell cultures simultaneously by IFA and Hoechst DNA fluorochrome staining methods. It was observed that the Photoshop-based image analysis on IFA stained slides was very valuable as a sensitive tool in providing quantitative assessment on the extent of contamination both per se and in comparison to cellularity of cell cultures. The technique could be useful in estimating the efficacy of anti-mycoplasma agents during decontaminating measures.

Structural transitions, ion mobility, and conductivity in CsSbF3(H2PO4)

Science.gov (United States)

Kavun, V. Ya.; Uvarov, N. F.; Slobodyuk, A. B.; Ulihin, A. S.; Kovaleva, E. V.; Zemnukhova, L. A.

2018-02-01

Structural transitions, ion mobility, and conductivity in CsSbF3(H2PO4) (I) have been investigated by the methods of 1H, 19F, 31P NMR (including 1H, 19F, 31P MAS NMR), DSC, X-ray diffraction, and impedance spectroscopy. It was found that the fundamental changes in 1H, 19F, 31P NMR spectra (above 390 K) were associated with the formation of a crystalline disorder phase I with high ionic mobility in the proton and fluoride sublattices, as a result of a phase transition in the 400-420 K range. In the same temperature range, the transition of PO2(OH)2- anions from the "rigid lattice" to fast reorientations takes place. Above 430 K, there occurs a transition from the crystalline disordered phase to the amorphous one. The types of ion mobility in CsSbF3(H2PO4) and its amorphous phase have been established and temperature ranges of their realization have been determined (150-450 K). According to the NMR data, the diffusion in the proton sublattice of the disordered crystalline and amorphous phases is preserved even at room temperature. The ionic conductivity in CsSbF3(H2PO4) reaches the values of 2.6 × 10-4 S/cm in the temperature range 410-425 K and decreases down to 2.0 × 10-5 S/cm upon transition to the amorphous phase (435-445 K).

The large second-harmonic generation of LiCs{sub 2}PO{sub 4} is caused by the metal-cation-centered groups

Energy Technology Data Exchange (ETDEWEB)

Cheng, Xiyue; Guo, Guo-Cong; Hong, Maochun; Deng, Shuiquan [State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter (FJIRSM), Chinese Academy of Sciences (CAS), Fuzhou (China); Whangbo, Myung-Hwan [State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter (FJIRSM), Chinese Academy of Sciences (CAS), Fuzhou (China); Department of Chemistry, North Carolina State University, Raleigh, NC (United States)

2018-04-03

We evaluated the individual atom contributions to the second harmonic generation (SHG) coefficients of LiCs{sub 2}PO{sub 4} (LCPO) by introducing the partial response functionals on the basis of first principles calculations. The SHG response of LCPO is dominated by the metal-cation-centered groups CsO{sub 6} and LiO{sub 4}, not by the nonmetal-cation-centered groups PO{sub 4} expected from the existing models and theories. The SHG coefficients of LCPO are determined mainly by the occupied orbitals O 2p and Cs 5p as well as by the unoccupied orbitals Cs 5d and Li 2p. For the SHG response of a material, the polarizable atomic orbitals of the occupied and the unoccupied states are both important. (copyright 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

The influence of interstitial water velocity on the migration of 85Sr and 137Cs in an aerated sandy soil layer

International Nuclear Information System (INIS)

Ohnuki, Toshihiko; Takebe, Shinichi; Yamamoto, Tadatoshi; Wadachi, Yoshiki

1983-01-01

The influence of interstitial water velocity on the migration of Sr-85 and Cs-137 in an aerated sandy soil layer was studied at different feed water velocities and feed times. As well known, it was found that Sr-85 migrated with interstitial water, but Cs-137 little migrated with interstitial water. The apparent migration velocity for each fraction corresponding to three concentrations (2 x 10 -2 , 1 x 10 -2 and 5 x 10 -3 μCi/g) of Sr-85 was further investigated. At constant interstitial water velocity (1cm/ min), different values were given for the apparent migration velocity of three fractions, and the fraction with thin concentration migrated faster. At constant feeding time (100hr), there was a linear relationship between apparent migration velocity of three fractions and interstitial water velocity, in the range of slow water velocity ( -2 and 5 x 10 -3 μCi/g) and interstitial water velocity, in the range of fast water velocity (> 1cm/min). (author)

Flexible All-Inorganic Perovskite CsPbBr3 Nonvolatile Memory Device.

Science.gov (United States)

Liu, Dongjue; Lin, Qiqi; Zang, Zhigang; Wang, Ming; Wangyang, Peihua; Tang, Xiaosheng; Zhou, Miao; Hu, Wei

2017-02-22

All-inorganic perovskite CsPbX 3 (X = Cl, Br, or I) is widely used in a variety of photoelectric devices such as solar cells, light-emitting diodes, lasers, and photodetectors. However, studies to understand the flexible CsPbX 3 electrical application are relatively scarce, mainly due to the limitations of the low-temperature fabricating process. In this study, all-inorganic perovskite CsPbBr 3 films were successfully fabricated at 75 °C through a two-step method. The highly crystallized films were first employed as a resistive switching layer in the Al/CsPbBr 3 /PEDOT:PSS/ITO/PET structure for flexible nonvolatile memory application. The resistive switching operations and endurance performance demonstrated the as-prepared flexible resistive random access memory devices possess reproducible and reliable memory characteristics. Electrical reliability and mechanical stability of the nonvolatile device were further tested by the robust current-voltage curves under different bending angles and consecutive flexing cycles. Moreover, a model of the formation and rupture of filaments through the CsPbBr 3 layer was proposed to explain the resistive switching effect. It is believed that this study will offer a new setting to understand and design all-inorganic perovskite materials for future stable flexible electronic devices.

Features of present day Cs 137 contamination of Bryansk-Belarusian Poles'e

International Nuclear Information System (INIS)

Kvasnikova, E.V.; Stukin, E.D.; Zhukova, O.M.; Germenchuk, M.G.; Zhukova, O.Mit.; Shagalova, E.D.; Bakarykava, Zh.V.; Kirienko, N.V.

2005-01-01

This article is devoted to estimation of changes of the area of radioactive pollution in Bryansk-Belarusian Poles'e due to intensity of landscape factors influence. Research of influence of geochemical conditions on transformation of soil pollution with Cs 137 was carried out on the catchment of small and medium size rivers: the Besed' river (Bryansk-Belarusian cesium spot), the Nesvich river (the territory of exclusion zone of Chernobyl NPP) (Belarus), the Moskovka river and the Oleshnya river (Russia) of Dnieper basin (Bryansk-Belarusian cesium spot). Investigation results have shown that soddy podsolic sandy soil under a pine forest resist Cs 137 migration, strongly fixing this radionuclide in a thin layer of the humus horizon lying under forest litter. In the processes of redistribution of Cs 137 in hydromorphous landscapes of Bryansk woodlands, vertical migration prevails above lateral one. In soils with redundant humidification Cs 137 significant transfer from the top 5-cm layer of soil occurs in comparison with automorphous soils. On arable lands there is an appreciable Cs 137 transfer in a horizontal direction and its accumulation on negative elements of relief. (authors)

The western Veil nebula (Image)

Science.gov (United States)

Glenny, M.

2009-12-01

The western Veil nebula in Cygnus. 15-part mosaic by Mike Glenny, Gloucestershire, taken over several months mostly in the autumn of 2008. 200mm LX90/f10 autoguided, Meade UHC filter, 0.3xFR/FF, Canon 20Da DSLR. Exposures each typically 10x360 secs at ISO1600, processed in Registax4, PixInsight (for flat field correction) & Photoshop CS.

Crystal field effect in the uranium compounds - model calculations for CsUF/sub 6/, Cs/sub 2/UCl/sub 6/ and UCl/sub 4/

Energy Technology Data Exchange (ETDEWEB)

Gajek, Z.; Mulak, J.; Faucher, M.

1987-01-01

A practical crystal field model allowing one to estimate the crystal field parameters from first principles is presented and applied to the actinide compounds. The model results directly from the renormalization (and reduction) procedure of the true Schroedinger equation for an effective Hamiltonian acting on the 5f spin-orbitals only. In practice this approach becomes convergent with the ab initio model of Newman. Three ionic uranium compounds: CsUF/sub 6/, Cs/sub 2/UCl/sub 6/ and UCl/sub 4/ have served as examples of the application. The results obtained, particularly for the first two compounds, are in good agreement with the experimental data. The contributions of different mechanisms responsible for the crystal field effect are discussed.

Photoshop® Assisted Spectroscopy: An Economical and Non-Destructive Method for Tracking Color Shift.

Science.gov (United States)

Wright, Kristi; Herro, Holly

Many historically and culturally significant objects from the mid-to-late 20 th century were created with media which contains light sensitive dyes that present problems for collection custodians and conservators. The conservation staff at the National Library of Medicine (NLM), National Institutes of Health, conducted a multi-phase project on the aging of ballpoint pen ink in a variety of enclosure types that ultimately culminated in the development of a new method to detect color shift in documents with light sensitive media. This article offers instructions on how to detect color shift in digitized materials using Photoshop® Assisted Spectroscopy.

Migration of cesium-137 through sandy soil layer effect of fine silt on migration

International Nuclear Information System (INIS)

Ohnuki, Toshihiko; Wadachi, Yoshiki

1983-01-01

The migration of 137 Cs through sandy soil layer was studied with consideration of the migration of fine silt by column method. It was found that a portion of fine silt migrated through the soil layer accompanying with 137 Cs. The mathematical migration model of 137 Cs involved the migration of fine silt through such soil layer was presented. This model gave a good accordance between calculated concentration distribution curve in sandy soil layer and effluent curve and observed those. So, this model seems to be advanced one for evaluating migration of 137 Cs in sandy soil layer with silt. (author)

Synthesis and crystal structure of hydrogen selenates K(HSeO4)(H2SeO4) and Cs(HSeO4)(H2SeO4)

International Nuclear Information System (INIS)

Troyanov, S.I.; Morozov, I.V.; Zakharov, M.A.; Kemnitz, E.

1999-01-01

Hydrogen selenates of the compositions K(HSeO 4 )(H 2 SeO 4 ) and Cs(HSeO 4 )(H 2 SeO 4 ) are synthesized by the reaction of alkali metal carbonates with an excess of the concentrated selenic acid. The X-ray diffraction study showed that both compounds are isostructural to the corresponding hydrogen sulfates. The difference in the systems of hydrogen bonding are caused by various combinations of the acceptor functions of the oxygen atoms in the HSeO 4 and H 2 SeO 4 groups

Level and origin of {sup 129}I and {sup 137}Cs in lichen samples (Cladonia alpestris) in central Sweden

Energy Technology Data Exchange (ETDEWEB)

Gomez-Guzman, J.M., E-mail: jm_gomez@us.e [Centro Nacional de Aceleradores (CNA), Accelerator Mass Spectrometry Unit, Avd. Tomas Alva Edison 7, Isla de Cartuja, Seville 41092 (Spain); Lopez-Gutierrez, J.M. [Centro Nacional de Aceleradores (CNA), Accelerator Mass Spectrometry Unit, Avd. Tomas Alva Edison 7, Isla de Cartuja, Seville 41092 (Spain); Department of Applied Physics, University of Seville, C. Virgen de Africa 7, Seville 41011 (Spain); Holm, E. [Norwegian Radiation Protection Authority, Grini Naearingspark 13, P.O. Box 55, 1332 Osteras (Norway); Pinto-Gomez, A.R. [Centro Nacional de Aceleradores (CNA), Accelerator Mass Spectrometry Unit, Avd. Tomas Alva Edison 7, Isla de Cartuja, Seville 41092 (Spain)

2011-02-15

Lichen is a symbiosis between algae and fungi. They have for decades been used as bioindicators for atmospheric deposition of heavy metals, organic compounds and radioactive elements. Especially the species Cladonia alpestris and Cladonia rangiferina are important for the food chain lichen-reindeer-man. The concentration of {sup 129}I was determined in lichen samples (Cladonia alpestris) contaminated by fallout from atmospheric nuclear tests explosions and the Chernobyl accident. The samples were collected at Lake Rogen District (62.3{sup o}N, 12.4{sup o}E) in central Sweden in the periods 1961-1975 and 1987-1998, and analysed with accelerator mass spectrometry (AMS) at CNA (Seville) to study its distribution in different layers. Data on the {sup 137}Cs activity measured previously were also included in this study. The {sup 129}I concentration ranged from (0.95 {+-} 0.13) x 10{sup 8} at g{sup -1} in 1961 in the uppermost layer to (14.2 {+-} 0.5) x 10{sup 8} at g{sup -1} in 1987 in deepest layer. The {sup 129}I/{sup 137}Cs atom ratio ranged between 0.12 and 0.27 for lichen samples collected in the period 1961-1975, indicating weapons tests fallout. For lichen samples collected between 1987 and 1998 the behaviour of {sup 137}Cs concentrations reflected Chernobyl fallout. The concentrations of the two radionuclides followed each other quite well in the profile, reflecting the same origin for both. From the point of view of the spatial distribution in the lichen, it appears that {sup 129}I was predominantly accumulated in the lowest layer, the opposite to {sup 137}Cs for which the highest amounts were detected systematically in the topmost layer of lichen. This vertical distribution is important for radioecology because lichen is the initial link in the food chain lichen-reindeer-man, and reindeer only graze the upper parts of lichen carpets. - Research highlights: {yields} This work shows the results for {sup 129}I in lichens collected in 1961-1975 and 1987

Cs0.49NbPS6

Directory of Open Access Journals (Sweden)

Hoseop Yun

2011-01-01

Full Text Available The quaternary thiophosphate, Cs0.49NbPS6, caesium hexathioniobiophosphate(V, has been synthesized by the reactive halide flux method. The title compound is isotypic with Rb0.46TaPS6 and is made up of a bicapped trigonal–biprismatic [Nb2S12] unit and a tetrahedral [PS4] group. The [Nb2S12] units linked by the [PS4] tetrahedra form infinite chains, yielding a three-dimensional network with rather large van der Waals gaps along the c axis in which the disordered Cs+ ions reside. The electrons released by the Cs atoms are transferred to the pairwise niobium metal site and there are substantial intermetallic Nb—Nb bonding interactions. This leads to a significant decrease of the intermetallic distance in the title compound compared to that in TaPS6. The classical charge balance of the title compound may be represented as [Cs+]0.49[Nb4.51+][P5+][S2−]4[S22−].

A quantitative model for estimating mean annual soil loss in cultivated land using 137Cs measurements

International Nuclear Information System (INIS)

Yang Hao; Zhao Qiguo; Du Mingyuan; Minami, Katsuyuki; Hatta, Tamao

2000-01-01

The radioisotope 137 Cs has been widely used to determine rates of cultivated soil loss, Many calibration relationships (including both empirical relationships and theoretical models) have been employed to estimate erosion rates from the amount of 137 Cs lost from the cultivated soil profile. However, there are important limitations which restrict the reliability of these models, which consider only the uniform distribution of 137 Cs in the plough layer and the depth. As a result, erosion rates they may be overestimated or underestimated. This article presents a quantitative model for the relation the amount of 137 Cs lost from the cultivate soil profile and the rate of soil erosion. According to a mass balance model, during the construction of this model we considered the following parameters: the remaining fraction of the surface enrichment layer (F R ), the thickness of the surface enrichment layer (H s ), the depth of the plough layer (H p ), input fraction of the total 137 Cs fallout deposition during a given year t (F t ), radioactive decay of 137 Cs (k), and sampling year (t). The simulation results showed that the amounts of erosion rates estimated using this model were very sensitive to changes in the values of the parameters F R , H s , and H p . We also observed that the relationship between the rate of soil loss and 137 Cs depletion is neither linear nor logarithmic, and is very complex. Although the model is an improvement over existing approaches to derive calibration relationships for cultivated soil, it requires empirical information on local soil properties and the behavior of 137 Cs in the soil profile. There is clearly still a need for more precise information on the latter aspect and, in particular, on the retention of 137 Cs fallout in the top few millimeters of the soil profile and on the enrichment and depletion effects associated with soil redistribution (i.e. for determining accurate values of F R and H s ). (author)

137Cs-migration in soils and its transfer to roe deer in an Austrian forest stand

International Nuclear Information System (INIS)

Strebl, F.; Gerzabek, M.H.; Karg, V.; Tataruch, F.

1996-01-01

The depth distribution of 137 Cs in an Austrian spruce forest stand was investigated in soil profiles sampled in thin layers (2 cm) and in pooled soil samples over an area of 200 ha. The 137 Cs concentrations both from Chernobyl and global fallout decrease exponentially with depth. Forty-six percent of Chernobyl-derived caesium and 26% from global fallout are still to be found in the litter layer; 137 Cs content in samples on organic matter as well as cation exchange capacity. Using a compartment model, average residence half-times of 5.3, 9.9, 1.78 and 0.8 years were calculated for the layers litter, 0-5 (Ah 1 ), 5-10 (Ah 2 ) and 10-20 cm (A/B) of mineral soil, respectively. Using the model predictions of soil contamination as a basis and considering that roe deer forage plants' rooting depths, the development of 137 Cs contamination of roe deer (Capreolus capreolus) (1987-1993) was well described by applying an aggregated transfer factor

Radioecological studies of {sup 137}Cs in limnological ecosystems. Biochemical states of {sup 137}Cs accumulated in killifish (Medaka, Oryzias latipes) meat

Energy Technology Data Exchange (ETDEWEB)

Miyake, Sadaaki; Motegi, Misako; Oosawa, Takashi; Nakazawa, Kiyoaki [Saitama Institute of Public Health, Urawa (Japan); Izumo, Yoshiro; Nakamura, Fumio

1997-07-01

Biochemical states of {sup 137}Cs accumulated in killifish`s (Medaka, Oryzias latipes) meat were investigated in order to elucidate the accumulation mechanism of the radionuclide in goldfish, Carassius auratus auratus, examined in our preceding report. Most of {sup 137}Cs radioactivity in the killifish`s raw meat accumulated this radionuclide in the radioactive freshwater, were found in the non-protein nitrogenous compound (NPNC) fraction (>92%), also in the killifish`s control raw meat mixed with {sup 137}Cs, the difference between both meat samples was not clear. As the results of gel filtration profiles on Sephadex G-25 for the NPNC fraction of these meats, each only one radioactive peak was shown, also similar to {sup 137}CsCl solution. Moreover, these peaks appeared at the same position. On the other hand, the peak positions absorbed at OD{sub 280nm} in the samples were different from those of each radioactive peak. It was so suggested that {sup 137}Cs accumulated in the killifish`s meat was shown not to be binding to protein`s composition. Furthermore, as the results on thin-layer chromatography, ion-exchange resin chromatography and reaction with {sup 137}Cs in samples and ammonium phosphomolybdate, {sup 137}Cs in the NPNC fraction of the killifish`s meat was not almost different from those of each control and {sup 137}CsCl solution. (author)

Effect of chemical pollution on forms of 137Cs, 90Sr and 239,240Pu in arctic soil studied by sequential extraction.

Science.gov (United States)

Puhakainen, M; Riekkinen, I; Heikkinen, T; Jaakkola, T; Steinnes, E; Rissanen, K; Suomela, M; Thørring, H

2001-01-01

The aim of the present study was to determine the forms of 137Cs, 90Sr and 239,240Pu occurring in different soil horizons using sequential extraction of samples taken from four sites located along a pollution gradient from the copper-nickel smelter at Monchegorsk in the Kola Peninsula, Russia, and from a reference site in Finnish Lapland in 1997. A selective sequential-leaching procedure was employed using a modification of the method of Tessier, Cambell and Bisson ((1979). Analytical Chemistry, 51, 844-851). For 137Cs the organic (O) and uppermost mineral (E1) layer were studied, for 90Sr and 239,240Pu only the uppermost organic layer (Of). The fraction of 137Cs occurring in readily exchangeable form in the organic layer was about 50% at the reference site and decreased as a function of pollution, being 15% at the most polluted site in the Kola Peninsula. There was a clear positive correlation in the O layer between the distance from the smelter and the percentage of 137Cs extracted in the readily exchangeable fraction (Spearman correlation rsp = 0.7805, p = 0.0001), whereas in the E1 layer no correlation was evident. The distribution of 90Sr in the Of layer was similar at all sites, with the highest amounts occurring in exchangeable form and bound to organic matter, whereas stable Sr showed a somewhat different distribution with the highest amount in the oxide fraction. Most of the 239,240Pu was bound to organic matter. Chemical pollution affected the exchangeable fraction of 239,240Pu, which was about 1% at the most polluted site and 4-6% at the other sites.

Concentration of "1"3"4Cs + "1"3"7Cs bonded to the organic fraction of sediments offshore Fukushima, Japan

International Nuclear Information System (INIS)

Ono, Tsuneo; Ambe, Daisuke; Kaeriyama, Hideki

2015-01-01

We conducted a sequential chemical extraction experiment for radiocesium ("1"3"4Cs + "1"3"7Cs) using 21 surface sediment samples and two sets of size-fractionated surface sediment samples collected offshore Fukushima. Our results support earlier reports in this area that organic substances in marine sediments have an apparently higher preference for radiocesium than mineral substances. Observations suggest that mineral and organic substances in the marine sediments offshore Fukushima have the same order of preference for radiocesium, primarily because of the existence of ionic competitors in seawater. The apparent preference of radiocesium for organic material is greater because of the partial coverage of sediment mineral surfaces by organic substances. By using these relationships, we created a 2-D map of radiocesium concentration in sediment organic fraction in offshore-Fukushima region. Combining our results with existing monitoring data of marine benthos in offshore-Fukushima sediments, we estimated a transfer coefficient of radiocesium from sediment organic materials to benthic polychaetes as less than 0.03-0.008. (author)

Formation of zeolite-like zinc 1,3,5-benzenetriphosphonate open-frameworks by topotactic pillaring of anionic layers.

Science.gov (United States)

Maeda, Kazuyuki; Takamatsu, Ryohei; Mochizuki, Miki; Kawawa, Kanako; Kondo, Atsushi

2013-08-07

An ab initio powder X-ray crystal structure analysis revealed that layered zinc 1,3,5-benzenetriphosphonates containing interlayer tetramethylammonium (ZBP-TMA) or 4,4'-bipyridinium cations (ZBP-bpy) are transformed to novel isomorphous 3D open-framework compounds ZBP-M (M: K, Rb, and Cs) by treatment in aqueous alkali metal chloride solutions. ZBP-Ms have a pillared layer-type of anionic framework containing 2D zigzag channels connected with cage-like spaces. The potassium atoms in ZBP-K are located near 8MR windows in the 2D zigzag channels, and the potassium cations are successfully exchanged with ammonium cations retaining the open-framework structure. The ammonium form (ZBP-NH4) showed remarkable cation exchange selectivity for Rb(+) and Cs(+) in a mixture of alkali metal cations. It is assumed that zinc ions partially dissolved from the starting layered ZBP precursors are intercalated in ZBP layers to form pillared layered 3D open-frameworks. These results clearly show that topotactic pillared layer approaches are applicable not only to zeolite-related materials but also to novel open-framework metal organophosphonates.

Digital Quantification of Goldmann Visual Fields (GVF) as a Means for Genotype-Phenotype Comparisons and Detection of Progression in Retinal Degenerations

Science.gov (United States)

Zahid, Sarwar; Peeler, Crandall; Khan, Naheed; Davis, Joy; Mahmood, Mahdi; Heckenlively, John; Jayasundera, Thiran

2015-01-01

Purpose To develop a reliable and efficient digital method to quantify planimetric Goldmann visual field (GVF) data to monitor disease course and treatment responses in retinal degenerative diseases. Methods A novel method to digitally quantify GVF using Adobe Photoshop CS3 was developed for comparison to traditional digital planimetry (Placom 45C digital planimeter; EngineerSupply, Lynchburg, Virginia, USA). GVFs from 20 eyes from 10 patients with Stargardt disease were quantified to assess the difference between the two methods (a total of 230 measurements per method). This quantification approach was also applied to 13 patients with X-linked retinitis pigmentosa (XLRP) with mutations in RPGR. Results Overall, measurements using Adobe Photoshop were more rapidly performed than those using conventional planimetry. Photoshop measurements also exhibited less inter- and intra-observer variability. GVF areas for the I4e isopter in patients with the same mutation in RPGR who were nearby in age had similar qualitative and quantitative areas. Conclusions Quantification of GVF using Adobe Photoshop is quicker, more reliable, and less-user dependent than conventional digital planimetry. It will be a useful tool for both retrospective and prospective studies of disease course as well as for monitoring treatment response in clinical trials for retinal degenerative diseases. PMID:24664690

Digital quantification of Goldmann visual fields (GVFs) as a means for genotype-phenotype comparisons and detection of progression in retinal degenerations.

Science.gov (United States)

Zahid, Sarwar; Peeler, Crandall; Khan, Naheed; Davis, Joy; Mahmood, Mahdi; Heckenlively, John R; Jayasundera, Thiran

2014-01-01

To develop a reliable and efficient digital method to quantify planimetric Goldmann visual field (GVF) data to monitor disease course and treatment responses in retinal degenerative diseases. A novel method to digitally quantify GVFs using Adobe Photoshop CS3 was developed for comparison to traditional digital planimetry (Placom 45C digital planimeter; Engineer Supply, Lynchburg, Virginia, USA). GVFs from 20 eyes from 10 patients with Stargardt disease were quantified to assess the difference between the two methods (a total of 230 measurements per method). This quantification approach was also applied to 13 patients with X-linked retinitis pigmentosa (XLRP) with mutations in RPGR. Overall, measurements using Adobe Photoshop were more rapidly performed than those using conventional planimetry. Photoshop measurements also exhibited less inter- and intraobserver variability. GVF areas for the I4e isopter in patients with the same mutation in RPGR who were nearby in age had similar qualitative and quantitative areas. Quantification of GVFs using Adobe Photoshop is quicker, more reliable, and less user dependent than conventional digital planimetry. It will be a useful tool for both retrospective and prospective studies of disease course as well as for monitoring treatment response in clinical trials for retinal degenerative diseases.

Asymmetric temporal integration of layer 4 and layer 2/3 inputs in visual cortex.

Science.gov (United States)

Hang, Giao B; Dan, Yang

2011-01-01

Neocortical neurons in vivo receive concurrent synaptic inputs from multiple sources, including feedforward, horizontal, and feedback pathways. Layer 2/3 of the visual cortex receives feedforward input from layer 4 and horizontal input from layer 2/3. Firing of the pyramidal neurons, which carries the output to higher cortical areas, depends critically on the interaction of these pathways. Here we examined synaptic integration of inputs from layer 4 and layer 2/3 in rat visual cortical slices. We found that the integration is sublinear and temporally asymmetric, with larger responses if layer 2/3 input preceded layer 4 input. The sublinearity depended on inhibition, and the asymmetry was largely attributable to the difference between the two inhibitory inputs. Interestingly, the asymmetric integration was specific to pyramidal neurons, and it strongly affected their spiking output. Thus via cortical inhibition, the temporal order of activation of layer 2/3 and layer 4 pathways can exert powerful control of cortical output during visual processing.

Intrinsic Lead Ion Emissions in Zero-Dimensional Cs4PbBr6 Nanocrystals

KAUST Repository

Yin, Jun; Zhang, Yuhai; Bruno, Annalisa; Soci, Cesare; Bakr, Osman; Bredas, Jean-Luc; Mohammed, Omar F.

2017-01-01

-energy UV emission at approximately 350 nm to the allowed optical transition of 3P1 to 1S0 in Pb2+ ions and the low-energy UV emission at approximately 400 nm to the charge-transfer state involved in the 0D NC host lattice (D-state). In the emissive Cs4PbBr6

Molecular CsF 5 and CsF 2 +

KAUST Repository

Rogachev, Andrey Yu.; Miao, Mao-sheng; Merino, Gabriel; Hoffmann, Roald

2015-01-01

D5h star-like CsF5, formally isoelectronic with known XeF5− ion, is computed to be a local minimum on the potential energy surface of CsF5, surrounded by reasonably large activation energies for its exothermic decomposition to CsF+2 F2, or to CsF3 (three isomeric forms)+F2, or for rearrangement to a significantly more stable isomer, a classical Cs+ complex of F5−. Similarly the CsF2+ ion is computed to be metastable in two isomeric forms. In the more symmetrical structures of these molecules there is definite involvement in bonding of the formally core 5p levels of Cs.

Molecular CsF 5 and CsF 2 +

KAUST Repository

Rogachev, Andrey Yu.

2015-06-03

D5h star-like CsF5, formally isoelectronic with known XeF5− ion, is computed to be a local minimum on the potential energy surface of CsF5, surrounded by reasonably large activation energies for its exothermic decomposition to CsF+2 F2, or to CsF3 (three isomeric forms)+F2, or for rearrangement to a significantly more stable isomer, a classical Cs+ complex of F5−. Similarly the CsF2+ ion is computed to be metastable in two isomeric forms. In the more symmetrical structures of these molecules there is definite involvement in bonding of the formally core 5p levels of Cs.

Coprecipitation of trace amounts of 137Cs and 85Sr with [Na(18-Crown-6]BPh4 from neutral and alkaline solutions

International Nuclear Information System (INIS)

Kulyukhin, S.A.; Konovalova, N.A.; Rumer, I.A.; Kamenskaya, A.N.; Mikheev, N.B.

2005-01-01

Coprecipitation of 137 Cs and 85 Sr with [Na(18-crown-6]BPh 4 solid phase from aqueous, aqueous-ethanolic, and alkaline solutions is studied. 137 C s and 85 Sr co-crystallize with [Na(18-crown-6]BPh 4 from aqueous and aqueous-ethanolic solutions. The cocrystallization coefficients D of 137 Cs and 85 Sr from aqueous solutions are 2.6 ± 0.5 and 3.3 ± 0.3, respectively. For aqueous-ethanolic solutions, the corresponding values are 4.4 ± 0.5 and 3.4 ± 0.4. In the alkaline solutions (0.1 and 1 M NaOH), 54-74% of 137 Cs and 37-51% of 85 Sr pass into the [Na(18-crown-6)]BPh 4 solid phase, depending on the crown ether concentration in the system [ru

A winning combination: the 3Cs of business continuity.

Science.gov (United States)

Glendon, Lee

2013-01-01

Contingency planning is a natural part of business life and is used across identified strategic, financial and operational risks. But is it being done well and is it the right approach all of the time? This paper shows how contingency planning forms one layer of a three-line defence termed 'the 3Cs of business continuity': contingency planning; continuity capability; crisis response. Collectively, 'the 3Cs' help organisations deliver a robust response to the risks that can be seen and those that cannot.

Morphing images to demonstrate potential surgical outcomes.

Science.gov (United States)

Hamilton, Grant S

2010-05-01

Morphing patient images to offer some demonstration of the intended surgical outcome can support shared expectations between patient and facial plastic surgeon. As part of the preoperative consultation, showing a patient an image that compares their face before surgery with what is planned after surgery can greatly enhance the surgical experience. This article refers to use of Photoshop CS3 for tutorial descriptions but any recent version of Photoshop is sufficiently similar. Among the topics covered are creating a before-and-after, rhinoplasty imaging, face- and brow-lift imaging, and removing wrinkles. Each section presents a step-by-step tutorial with graphic images demonstrating the computer screen and Photoshop tools. Copyright 2010 Elsevier Inc. All rights reserved.

Inventories and fluxes of 137Cs in the Syrian land

International Nuclear Information System (INIS)

Al-Masri, M. S.; Amin, Y.

2005-03-01

Cesium-137 inventories and atmospheric fluxes have been determined using radiocesium distributions in undistributed soil profiles, collected from 38 sites distributed all over the Syrian lands. Results have shown that 137 Cs inventories determination by Soil Layers Sum Method is more accurate than the Integration Method, where the best curve fitting of 137 Cs distribution with depth is difficult to establish. 137 Cs inventories ranged from 441 Bq.m - 2 and 13312 Bq.m - 2 using the Layers Sum Method with a mean value of 3679 Bq.m - 2; the highest values observed were in the coastal, middle and north east regions. This is due to the fact that most of Chernobyl accident atmospheric fall-out of cesium 137 had entered the Syrian land came from the west boarders (Mediterranean sea). While the lowest values were found to be in the samples collected from the east south region. In addition, 137 Cs flux ranged from 3.1 kBq m - 2y - 1 and 527.8 kBq m - 2 y - 1 with a mean value of 65.7 kBq m - 2y - 1. Moreover, there was a semi linear relationship found between 137 Cs flux and the height above sea level. While no linear relationship was found between 137 Cs flux and annual rainfall. On the other hand, the external radiation dose to Syrians that due to gamma-rays emitted from cesium 137 decay has been determined and reached a mean value of 166μ Sv.y - 1. This value is about 20% of the radiation dose received by the Syrian from naturally occurring radionuclides in soil. (Author)

A novel vanadosilicate with hexadeca-coordinated Cs{sup +} ions as a highly effective Cs{sup +} remover

Energy Technology Data Exchange (ETDEWEB)

Datta, Shuvo Jit; Moon, Won Kyung; Choi, Do Young; Hwang, In Chul; Yoon, Kyung Byung [Sogang Univ., Seoul (Korea, Republic of). Korea Center for Artificial Photosynthesis

2014-07-07

The effective removal of {sup 137}Cs{sup +} ions from contaminated groundwater and seawater and from radioactive nuclear waste solutions is crucial for public health and for the continuous operation of nuclear power plants. Various {sup 137}Cs{sup +} removers have been developed, but more effective {sup 137}Cs{sup +} removers are still needed. A novel microporous vanadosilicate with mixed-valence vanadium (V{sup 4+} and V{sup 5+}) ions is now reported, which shows an excellent ability for Cs{sup +} capture and immobilization from groundwater, seawater, and nuclear waste solutions. This material is superior to other known materials in terms of selectivity, capacity, and kinetics, and at very low Cs{sup +} concentrations, it was found to be the most effective material for the removal of radioactive Cs{sup +} ions under the test conditions. This novel vanadosilicate also contains hexadeca-coordinated Cs{sup +} ions, which corresponds to the highest coordination number ever described.

X-ray enhancement of CsI:Eu{sup 2+} radioluminescence

Energy Technology Data Exchange (ETDEWEB)

Leblans, P., E-mail: paul.leblans@agfa.com [Agfa-HealthCare NV, Septestraat 27, B-2640 Mortsel (Belgium); Struye, L.; Elen, S.; Mans, I. [Agfa-HealthCare NV, Septestraat 27, B-2640 Mortsel (Belgium); Vrielinck, H.; Callens, F. [Electron Magnetic Resonance Research Group, Department of Solid State Sciences, Ghent University, Krijgslaan 281-S1, B-9000 Gent (Belgium)

2015-09-15

CsI:Eu{sup 2+} needle crystal layers were produced by Physical Vapour Deposition (PVD). The luminescence properties were studied before and after thermal anneal. It was shown by Electron Paramagnetic Resonance (EPR) that annealing produces Eu{sup 2+} monomer centres, probably starting from Eu clusters in the needle crystalline layers. These centres seem structurally very similar to the Eu{sup 2+} monomer centres in annealed CsBr:Eu{sup 2+} needle layers. They give rise to a narrow luminescence band peaking at about 450 nm (2.76 eV) at room temperature, both under X-ray and UV excitation. The luminescence intensity of as-deposited layers is low. Annealing enhances photo- and radioluminescence on average by a factor of 1.5–3. Surprisingly, further sensitization of radioluminescence with a factor of up to 7 is possible by exposing the annealed needle layers to X-rays or UV, while in contrast, UV excited luminescence is slightly reduced. X-ray enhancement thus leads to a structured scintillator with a conversion efficiency of about 42,000 photons/MeV upon X-ray excitation. A similar radioluminescence enhancement is observed for annealed CsI:Eu{sup 2+} fine powder, but not for large single crystals or conglomerated polycrystals. The measurements and observations are consistent with Eu{sup 2+} monomer centres stabilized by water molecules. These molecules are incorporated via annealing, and that this happens when the morphology is such that water can diffuse throughout the volume of the crystals. The presence of stabilized Eu{sup 2+} monomers is necessary to enhance radioluminescence by X-ray exposure. A mechanism is proposed for the phenomenon.

Distribution of radioactive "1"3"7Cs and "1"3"4Cs in river water and bottom sand for major rivers at Minami-Soma City in Fukushima

International Nuclear Information System (INIS)

Kajimoto, Tsuyoshi; Endo, Satoru; Shizuma, Kiyoshi; Naganuma, Takeshi

2013-01-01

A nuclear power plant accident, which occurred on March 11, 2011, caused severe radioactive contamination in Fukushima. We initiated an environmental radioactive survey in Minami-Soma City the following October. The city is located approximately 10-40 km north of the TEPCO's Fukushima Daiichi Nuclear Power Plant. The study reported here involves an environmental radioactive survey conducted along three rivers and their tributary streams. Water and bottom sands were collected from four to six sampling locations along each river. Water samples (1 L) were dried on thin Teflon sheets, and gamma-ray measurements were performed with a well-type Ge detector. Sand samples were homogenized after drying, and approximately 50 g were measured for gamma-rays with a low-background coaxial-type Ge detector. The Cs concentrations ("1"3"7Cs+"1"3"4Cs) were determined to be 10,000-20,000 Bq/kg in the bottom sand collected from the upper reaches of the rivers, whereas the concentrations measured from samples collected near coastal down reaches were measured at about 200 Bq/kg. The Cs concentrations measured in river water were about 0.8 Bq/L in the upper reaches of the rivers and 0.3 Bq/L in the lower reaches, indicating that the Cs concentration in water is quite low. It is necessary to study the behavior of the contaminants in the upper reaches of the river system, and determine if they will move to the down stream area hereafter. (author)

Distribution of radioactive "1"3"7Cs and "1"3"4Cs in river water and bottom sand for major rivers at Minami-Soma City in Fukushima

International Nuclear Information System (INIS)

Kajimoto, Tsuyoshi; Endo, Satoru; Shizuma, Kiyoshi; Naganuma, Takeshi

2012-01-01

A nuclear power plant accident, which occurred on March 11, 2011, caused severe radioactive contamination in Fukushima. We initiated an environmental radioactive survey in Minami-Soma City the following October. The city is located approximately 10-40 km north of the TEPCO's Fukushima Daiichi Nuclear Power Plant. The study reported here involves an environmental radioactive survey conducted along three rivers and their tributary streams.Water and bottom sands were collected from four to six sampling locations along each river. Water samples (1 L) were dried on thin Teflon sheets, and gamma-ray measurements were performed with a well-type Ge detector. Sand samples were homogenized after drying, and approximately 50 g were measured for gamma-rays with a low-background coaxial-type Ge detector. The Cs concentrations ("1"3"7Cs+"1"3"4Cs) were determined to be 10,000-20,000 Bq/kg in the bottom sand collected from the upper reaches of the rivers, whereas the concentrations measured from samples collected near coastal down reaches were measured at about 200 Bq/kg. The Cs concentrations measured in river water were about 0.8 Bq/L in the upper reaches of the rivers and 0.3 Bq/L in the lower reaches, indicating that the Cs concentration in water is quite low. It is necessary to study the behavior of the contaminants in the upper reaches of the river system, and determine if they will move to the down stream area hereafter. (author)

Probing molecules on a surface by Cs+ reactive ion scattering: identification of C2Hx (x≤4) hydrocarbons

International Nuclear Information System (INIS)

Kang, H.; Lee, C.W.; Hwang, C.H.; Kim, C.M.

2003-01-01

We studied molecular species appearing in the reactions of ethylene on a Pt(1 1 1) surface by the technique of Cs + reactive ion scattering (Cs + RIS). Dehydrogenation reaction of ethylene was examined for a surface temperature range of 100-800 K, and the RIS result verified the well-known sequence of forming di-σ-bonded ethylene (-CH 2 -CH 2 -), ethylidyne (≡C-CH 3 ), CH, and then surface carbons, as the temperature increased. In particular, the intermediate species in the conversion of ethylene to ethylidyne was closely investigated, which showed the presence of an ethylidene intermediate (≡CH-CH 3 ). In a study of H/D exchange reactions between surface C 2 D 4 and H, we successfully identified the ethylenes in which several deuterium atoms were substituted by hydrogen (C 2 D 4-x H x ,x=0-4), and quantitatively determined their relative populations. These examples demonstrate the ability of the Cs + RIS method to identify small hydrocarbons and their isotope-exchanged species on surfaces

Organic-Inorganic Hybrid Interfacial Layer for High-Performance Planar Perovskite Solar Cells.

Science.gov (United States)

Yang, Hao; Cong, Shan; Lou, Yanhui; Han, Liang; Zhao, Jie; Sun, Yinghui; Zou, Guifu

2017-09-20

4,7-Diphenyl-1,10-phenanthroline (Bphen) is an efficient electron transport and hole blocking material in organic photoelectric devices. Here, we report cesium carbonate (Cs 2 CO 3 ) doped Bphen as cathode interfacial layer in CH 3 NH 3 PbI 3-x Cl x based planar perovskite solar cells (PSCs). Investigation finds that introducing Cs 2 CO 3 suppresses the crystallization of Bphen and benefits a smooth interface contact between the perovskite and electrode, resulting in the decrease in carrier recombination and the perovskite degradation. In addition, the matching energy level of Bphen film in the PSCs effectively blocks the holes diffusion to cathode. The resultant power conversion efficiency (PCE) achieves as high as 17.03% in comparison with 12.67% of reference device without doping. Besides, experiments also demonstrate the stability of PSCs have large improvement because the suppressed crystallization of Bphen by doping Cs 2 CO 3 as a superior barrier layer blocks the Ag atom and surrounding moisture access to the vulnerable perovskite layer.

Parametric study of the sorption of Cs(I) and Sr(II) on mixture of bentonite and magnetite using SCM + IEXM

International Nuclear Information System (INIS)

Filipska, H.; Stamberg, K.

2005-01-01

of sorption, K(Cs/Sr), on total KD, % of sorption for Cs and Sr and for their individual species, etc. The individual quantities were related to the mass of bentonite and/or magnetite or to the type of functional group mentioned (edge and/or layer sites). From the results it is evident that the sorption selectivity depends not only on pH and type of sorbent, but also on the type of functional group; e.g., in the pH interval studied (4-9), the sorption of Cs is more selective than sorption of Sr on layer sites, on edge sites it is vice versa. On the whole, the sorption reactions of Cs(I) and Sr(II) taking place on layer sites play the most important role in the sorption process. (authors)

P-T-x phase diagrams of MeF-UF4(Me=Li-Cs) systems

International Nuclear Information System (INIS)

Korenev, Yu.M.; Rykov, A.N.; Varkov, M.V.; Novoselova, A.V.

1988-01-01

Vapor composition and general pressure at three-phase equilibria in the MeF-UF 4 (Me=Li-Cs) systems are calculated using the values of independent component activities obtained earlier together with the data on fusibility diagrams. P-T and T-x projections of phase diagrams of these systems are constructed

Interface engineering of CsPbBr3/TiO2 heterostructure with enhanced optoelectronic properties for all-inorganic perovskite solar cells

Science.gov (United States)

Qian, Chong-Xin; Deng, Zun-Yi; Yang, Kang; Feng, Jiangshan; Wang, Ming-Zi; Yang, Zhou; Liu, Shengzhong Frank; Feng, Hong-Jian

2018-02-01

Interface engineering has become a vital method in accelerating the development of perovskite solar cells in the past few years. To investigate the effect of different contacted surfaces of a light absorber with an electron transporting layer, TiO2, we synthesize CsPbBr3/TiO2 thin films with two different interfaces (CsBr/TiO2 and PbBr2/TiO2). Both interfacial heterostructures exhibit enhanced visible light absorption, and the CsBr/TiO2 thin film presents higher absorption than the PbBr2/TiO2 interface, which is attributed to the formation of interface states and the decreased interface bandgap. Furthermore, compared with the PbBr2/TiO2 interface, CsBr/TiO2 solar devices present larger output short circuit current and shorter photoluminescence decay time, which indicates that the CsBr contacting layer with TiO2 can better extract and separate the photo-induced carriers. The first-principles calculations confirm that, due to the existence of staggered gap (type II) offset junction and the interface states, the CsBr/TiO2 interface can more effectively separate the photo-induced carriers and thus drive the electron transfer from the CsPbBr3 perovskite layer to the TiO2 layer. These results may be beneficial to exploit the potential application of all-inorganic perovskite CsPbBr3-based solar cells through the interface engineering route.

How to optimize radiological images captured from digital cameras, using the Adobe Photoshop 6.0 program.

Science.gov (United States)

Chalazonitis, A N; Koumarianos, D; Tzovara, J; Chronopoulos, P

2003-06-01

Over the past decade, the technology that permits images to be digitized and the reduction in the cost of digital equipment allows quick digital transfer of any conventional radiological film. Images then can be transferred to a personal computer, and several software programs are available that can manipulate their digital appearance. In this article, the fundamentals of digital imaging are discussed, as well as the wide variety of optional adjustments that the Adobe Photoshop 6.0 (Adobe Systems, San Jose, CA) program can offer to present radiological images with satisfactory digital imaging quality.

137Cs-migration in soils and its transfer to roe deer in an Austrian forest stand

International Nuclear Information System (INIS)

Strebl, F.; Gerzabek, M. H.; Karg, V.; Tataruch, F.

1996-03-01

The depth distribution of 137 Cs in an Austrian spruce forest stand was investigated in soil profiles sampled in thin layers (2 cm) and in pooled soil samples over an area of 200 ha. The 137 Cs concentrations both from Chernobyl and global fallout decrease exponentially with depth. Forty-six percent of Chernobyl-derived cesium and 26 % from global fallout are still to be found in the litter layer; 137 Cs content in samples on organic matter as well as cation exchange capacity. Using a compartment model, average residence half-times of 5.3, 9.9, 1.78 and 0.8 years were calculated for the layers litter, 0-5 (Ah 1 ), 5-10 (Ah 2 ) and 10-20 cm (A/B) of mineral soil, respectively. Using the model predictions of soil contamination as a basis and considering the roe deer forage plants' rooting depths, the development of 137 Cs contamination of roe deer (Capreolus capreolus) (1987 - 1993) was well described by applying an aggregated transfer factor. (author)

Distribution of dendritic cells expressing dendritic cell-specific ICAM-3-grabbing non-integrin (DC-SIGN, CD209): Morphological analysis using a novel Photoshop-aided multiple immunohistochemistry technique.

Science.gov (United States)

Masuda, Akihiro; Nishikawa, Toshio

2014-08-01

The distribution of dendritic cells (DCs) expressing DC-specific ICAM-3-grabbing non-integrin (DC-SIGN, CD209) and the morphological interaction of DC-SIGN⁺ DCs with other cells, especially B cells, in tonsillar and other lymphoid tissues were investigated by multiple immunohistochemistry (IHC) using the graphics editing program Photoshop, which enabled staining with 4 or more antibodies in formalin-fixed paraffin sections. Images obtained by repetition of conventional IHC using diaminobenzidine color development in a tissue section were processed on Photoshop for multiple staining. DC-SIGN⁺ DCs were present in the area around the lymphoid follicles and formed a DC-SIGN⁺ DC-rich area, and these cells contacted not only T cells, fascin⁺ DCs, and blood vessels but also several subsets of B cells simultaneously, including naïve and memory B cells. DC-SIGN⁺ DCs may play an important role in the regulation of the immune response mediated by not only T cells but also B cells. The multiple IHC method introduced in the present study is a simple and useful method for analyzing details of complex structures. Because this method can be applied to routinely processed paraffin sections with conventional IHC with diaminobenzidine, it can be applied to a wide variety of archival specimens.

Crystal structure of Cs3H(SeO4)2 (T=295 K) and its changes in phase transformations

International Nuclear Information System (INIS)

Merinov, B.V.; Bolotina, N.B.; Baranov, A.I.; Shuvalov, L.A.

1988-01-01

Crystal structure of Cs 3 H(SeO 4 ) 2 3 phase at T=295 K is decoded by X-ray diffraction data. Monoclinic cell parameters are improved: a=10.903(3), b=6.390(8), c=8.452(2)A, β=112.46(1) deg, V=544 A 3 , Z=2, sp. gr. C2/m. Structural peculiarities of 3↔2↔1 phase transitions in Cs 3 H(SeO 4 ) 2 and proton conductivity mechanism in superionic phase are considered

Layer-by-layer assembly of type I collagen and chondroitin sulfate on aminolyzed PU for potential cartilage tissue engineering application

Science.gov (United States)

He, Xianyun; Wang, Yingjun; Wu, Gang

2012-10-01

In this paper, a two-step method was used to synthesize a biodegradable polyurethane (PU) composed of L-lysine ethyl ester diisocyanate (LDI), poly(ɛ-caprolactone) diols (PCL-diol) and 1,4:3,6-dianhydro-D-sorbitol (isosorbide). Amino groups were introduced onto the surface of the PU membrane by an amination reacting with 1,3-propanediamine to produce polycationic substratum. And then, type I collagen (Col) and chondroitin sulfate (CS) were deposited alternately on the polycationic substratum through layer-by-layer (LBL) assembly technology. The FTIR and 1H NMR results showed that the polyurethane was successfully synthesized. Rhodamine B isothiocyanate (RBITC) fluorescence spectrum indicated that amino groups were successfully introduced onto the PU surface. The results of quartz-crystal microbalance (QCM) and RBITC-Col fluorescence spectroscopy monitoring the LBL assemble process presented that the Col/CS deposited alternately on the PU surface. X-ray photoelectron spectroscopy (XPS) results displayed that the CS deposited on the PU surface as well. The surface of the assembled PU became even smoother observed from the surface morphology by atomic force microscopy (AFM) imaging. The hydrophilicity of the PU membrane was greatly enhanced though the modification of LBL assembly. The PU modified with the adsorption of Col/CS may be a potential application for cartilage tissue engineering due to its created mimicking chondrogenic environment.

Ternary rare-earth halides of the A2MX5 type (A = K, In, NH4, Rb, Cs; X = Cl, Br, I)

International Nuclear Information System (INIS)

Meyer, G.; Soose, J.; Moritz, A.; Vitt, V.; Holljes, T.

1985-01-01

Ternary rare-earth (=M) chlorides, bromides, and iodides In 2 MCl 5 , (NH 4 ) 2 MCl 5 , Rb 2 MCl 5 , Cs 2 MCl 5 , CsRbMCl 5 , K 2 MBr 5 , Rb 2 MBr 5 , K 2 MI 5 , and Rb 2 MI 5 have been synthesized. Single crystals of In 2 PrCl 5 , Rb 2 PrCl 5 , K 2 PrBr 5 , and K 2 PrI 5 were grown and the structures refined. The other halides were characterized by X-ray powder patterns. They are isotypic either with K 2 PrCl 5 (orthorhombic, Pnma, Z = 4, hexagonal arrangement of chains of edge-connected polyhedra [PrX 7 ]) or with Cs 2 DyCl 5 (orthorhombic, Pbnm, Z = 4, hexagonal arrangement of cis-corner-connected octahedra [DyCl 6 ]) which may be discriminated in structure field diagrams. The thermal expansion was investigated for Cs 2 LuCl 5 and Rb 2 PrX 5 (X = Cl, Br, I). (author)

Asymmetric Temporal Integration of Layer 4 and Layer 2/3 Inputs in Visual Cortex

OpenAIRE

Hang, Giao B.; Dan, Yang

2010-01-01

Neocortical neurons in vivo receive concurrent synaptic inputs from multiple sources, including feedforward, horizontal, and feedback pathways. Layer 2/3 of the visual cortex receives feedforward input from layer 4 and horizontal input from layer 2/3. Firing of the pyramidal neurons, which carries the output to higher cortical areas, depends critically on the interaction of these pathways. Here we examined synaptic integration of inputs from layer 4 and layer 2/3 in rat visual cortical slices...

Chemical information on tank supernatants, Cs adsorption from tank liquids onto Hanford sediments, and field observations of Cs migration from past tank leaks

Energy Technology Data Exchange (ETDEWEB)

Serne, R.J.; Zachara, J.M.; Burke, D.S.

1998-01-01

Borehole gamma-logging profiles beneath the SX-Tank Farm suggest that contamination from Cs-137 extends to at least a depth of 40 m (130 ft), and may extend even deeper. What is presently not known is the pathway that Cs-137 has taken to reach these depths. In this report we provide an analysis of the chemistry of tank supernates with emphasis on the REDOX waste stream disposed in SX tanks, Cs chemistry in aqueous solutions and adsorption properties onto minerals, available data on Cs adsorption onto Hanford sediments, and information on Cs migration from other Hanford tank leaks that have been studied. The data in this report was used to help guide the vadose zone transport analysis of the SX Tank Farm presented in a companion report. The goal of the vadose zone transport modelling is to attempt to explain the depth and extent of the Cs-137 plume under the SX Tank farm, specifically in the vicinity of the greatest leak, near the SX-109 Tank as inferred from the gamma logs (DOE 1996). In solution Cs is present as the monovalent cation and shows very little tendency to form aqueous complexes with inorganic or organic ligands. Cs is expected to adsorb primarily onto selective minerals that have unique adsorption sites. The small Cs{sup +} ion is accommodated on these frayed edge and interlayer sites. Adsorption within the interlayers often leads to collapse of the layers such that the Cs{sup +} ion is effectively trapped and not readily exchangeable by all other common cations. The degree of adsorption is thus only moderately dependent on the types and high concentrations of other cations in leaking tank liquors.

Chemical information on tank supernatants, Cs adsorption from tank liquids onto Hanford sediments, and field observations of Cs migration from past tank leaks

International Nuclear Information System (INIS)

Serne, R.J.; Zachara, J.M.; Burke, D.S.

1998-01-01

Borehole gamma-logging profiles beneath the SX-Tank Farm suggest that contamination from Cs-137 extends to at least a depth of 40 m (130 ft), and may extend even deeper. What is presently not known is the pathway that Cs-137 has taken to reach these depths. In this report we provide an analysis of the chemistry of tank supernates with emphasis on the REDOX waste stream disposed in SX tanks, Cs chemistry in aqueous solutions and adsorption properties onto minerals, available data on Cs adsorption onto Hanford sediments, and information on Cs migration from other Hanford tank leaks that have been studied. The data in this report was used to help guide the vadose zone transport analysis of the SX Tank Farm presented in a companion report. The goal of the vadose zone transport modelling is to attempt to explain the depth and extent of the Cs-137 plume under the SX Tank farm, specifically in the vicinity of the greatest leak, near the SX-109 Tank as inferred from the gamma logs (DOE 1996). In solution Cs is present as the monovalent cation and shows very little tendency to form aqueous complexes with inorganic or organic ligands. Cs is expected to adsorb primarily onto selective minerals that have unique adsorption sites. The small Cs + ion is accommodated on these frayed edge and interlayer sites. Adsorption within the interlayers often leads to collapse of the layers such that the Cs + ion is effectively trapped and not readily exchangeable by all other common cations. The degree of adsorption is thus only moderately dependent on the types and high concentrations of other cations in leaking tank liquors

Distribution of {sup 90} Sr and {sup 137} Cs in vertical soil sections of the Chernobyl exclusion zone.; Raspredelenie form nakhozhdeniya {sup 90} Sr i {sup 137} Cs po vertikal`nym pochvennym razrezam Zony otchuzhdeniya ChAEhS.

Energy Technology Data Exchange (ETDEWEB)

Bondarenko, G N; Kononenko, L.V. [AN Ukrainskoj SSR, Kiev (Ukraine). Inst. Geokhimii i Fiziki Mineralov

1994-12-31

Water-soluble, exchangeable and acid-soluble (IM HCI) forms of {sup 90} Sr and {sup 137} Cs were determined in 15 layer-by-layer (1 cm) samples of podzolis and peaty soils from the Chernobyl exclusion zone taken in 1991 and 1992. Positions of centers of {sup 137} Cs and {sup 90} Sr supply as well as their water-soluble and exchangeable forms were estimated. The data obtained testify to deceleration of vertical migration of {sup 137} Cs in soils till the early 90th. The conclusion is made on evolution of dominating mechanisms of vertical migration of radionuclides. It consists in a decrease of the lessivage significance.

Performance of LiAlloy/Ag(2)CrO(4) Couples in Molten CsBr-LiBr-KBr Eutectic

International Nuclear Information System (INIS)

GUIDOTTI, RONALD A.; REINHARDT, FREDERICK W.

1999-01-01

The performance of Li-alloy/CsBr-LiBr-KBr/Ag(sub 2)CrO(sub 4) systems was studied over a temperature range of 250 C to 300 C, for possible use as a power source for geothermal borehole applications. Single cells were discharged at current densities of 15.8 and 32.6 mA/cm(sup 2) using Li-Si and Li-Al anodes. When tested in 5-cell batteries, the Li-Si/CsBr-LiBr-KBr/Ag(sub 2)CrO(sub 4) system exhibited thermal runaway. Thermal analytical tests showed that the Ag(sub 2)CrO(sub 4) cathode reacted exothermically with the electrolyte on activation. Consequently, this system would not be practical for the envisioned geothermal borehole applications

Distribution of the radionuclide 137Cs in the soils of a wet mountainous forest in Taiwan

International Nuclear Information System (INIS)

Chiu, C.-Y.; Lai, S.-Y.; Lin, Y.-M.; Chiang, H.-C.

1999-01-01

The behavior of 137 Cs was studied in the Yuanyang lake ecosystem, a wet mountainous forest in subtropical Taiwan. Soils investigated are either partially podzolic soils or nearly pure peats with a high organic matter concentration in the surface layer. Concentration of 137 Cs was highest in the organic surface layers, particularly in the Oe horizon or in the underlying A horizon. The downwards migration to the mineral horizons is limited, in spite of the high rainfall. Topography is a critical factor for the distribution of 137 Cs. It is shown that the concentration of 137 Cs is highest at the foot of the slope and lower near the summit and near the lakeshore. The variation of the concentration along the landscape has been attributed to erosion-deposition in combination with surface run-off of the undisturbed forest. The amount of 137 Cs in the site studied is significantly higher than at any other place in Taiwan. The accumulation of 137 Cs is attributed to the high rainfall, which brought large amounts of 137 Cs with the precipitation in the early 1960s. A very remarkable feature of the ecosystem is that 137 Cs is not leached to the subsoils, but is stored in the biomass. Due to permanent recycling it remains available, without being leached downward

Distribution of 137Cs in the Surface Soil of Serpong Nuclear Site

International Nuclear Information System (INIS)

Lubis, E.

2011-01-01

The distribution of 137 Cs in the surface soil layer of Serpong Nuclear Site (SNS) was investigated by field sampling. The Objectives of the investigation is finding the profile of 137 Cs distribution in the surface soil and the T f value that can be used for estimation of radiation dose from livestock product-man pathways. The results indicates that the 137 Cs activity in surface soil of SNS is 0.80 ± 0.29 Bq/kg, much lower than in the Antarctic. The contribution value of 137 Cs from the operation of G.A. Siwabessy Reactor until now is undetectable. The T f of 137 Cs from surface soil to Panisetum Purpureum, Setaria Spha Celata and Imperata Cylindrica grasses were 0.71 ± 0.14, 0.84 ± 0.27 and 0.81 ± 0.11 respectively. The results show that value of the transfer factor of 137 Cs varies between cultivated and uncultivated soil and also with the soils with thick humus. (author)

Distribution of 137Cs In the Surface Soil of Serpong Nuclear Site

Directory of Open Access Journals (Sweden)

E. Lubis

2011-08-01

Full Text Available The distribution of 137Cs in the surface soil layer of Serpong Nuclear Site (SNS was investigated by field sampling. The Objectives of the investigation is finding the profile of 137Cs distribution in the surface soil and the Tf value that can be used for estimation of radiation dose from livestock product-man pathways. The results indicates that the 137Cs activity in surface soil of SNS is 0.80 ± 0,29 Bq/kg, much lower than in the Antarctic. The contribution value of 137Cs from the operation of G.A.Siwabessy Reactor until now is undetectable. The Tf of 137Cs from surface soil to Panisetum Purpureum, Setaria Spha Celata and Imperata Cylindrica grasses were 0.71 ± 0.14, 0.84 ± 0.27 and 0.81 ± 0.11 respectively. The results show that value of the transfer factor of 137Cs varies between cultivated and uncultivated soil and also with the soils with thick humus

First-principles study of paraelectric and ferroelectric CsH2PO4 including dispersion forces: Stability and related vibrational, dielectric, and elastic properties

Science.gov (United States)

Van Troeye, Benoit; van Setten, Michiel Jan; Giantomassi, Matteo; Torrent, Marc; Rignanese, Gian-Marco; Gonze, Xavier

2017-01-01

Using density functional theory (DFT) and density functional perturbation theory (DFPT), we investigate the stability and response functions of CsH2PO4 , a ferroelectric material at low temperature. This material cannot be described properly by the usual (semi)local approximations within DFT. The long-range e--e- correlation needs to be properly taken into account, using, for instance, Grimme's DFT-D methods, as investigated in this work. We find that DFT-D3(BJ) performs the best for the members of the dihydrogenated alkali phosphate family (KH2PO4 , RbH2PO4 , CsH2PO4 ), leading to experimental lattice parameters reproduced with an average deviation of 0.5%. With these DFT-D methods, the structural, dielectric, vibrational, and mechanical properties of CsH2PO4 are globally in excellent agreement with the available experiments (<2 % MAPE for Raman-active phonons). Our study suggests the possible existence of a new low-temperature phase of CsH2PO4 , not yet reported experimentally. Finally, we report the implementation of DFT-D contributions to elastic constants within DFPT.

Ce3+-Doping to Modulate Photoluminescence Kinetics for Efficient CsPbBr3 Nanocrystals Based Light-Emitting Diodes.

Science.gov (United States)

Yao, Ji-Song; Ge, Jing; Han, Bo-Ning; Wang, Kun-Hua; Yao, Hong-Bin; Yu, Hao-Lei; Li, Jian-Hai; Zhu, Bai-Sheng; Song, Ji-Zhong; Chen, Chen; Zhang, Qun; Zeng, Hai-Bo; Luo, Yi; Yu, Shu-Hong

2018-03-14

Inorganic perovskite CsPbBr 3 nanocrystals (NCs) are emerging, highly attractive light emitters with high color purity and good thermal stability for light-emitting diodes (LEDs). Their high photo/electroluminescence efficiencies are very important for fabricating efficient LEDs. Here, we propose a novel strategy to enhance the photo/electroluminescence efficiency of CsPbBr 3 NCs through doping of heterovalent Ce 3+ ions via a facile hot-injection method. The Ce 3+ cation was chosen as the dopant for CsPbBr 3 NCs by virtue of its similar ion radius and formation of higher energy level of conduction band with bromine in comparison with the Pb 2+ cation to maintain the integrity of perovskite structure without introducing additional trap states. It was found that by increasing the doping amount of Ce 3+ in CsPbBr 3 NCs to 2.88% (atomic percentage of Ce compared to Pb) the photoluminescence quantum yield (PLQY) of CsPbBr 3 NCs reached up to 89%, a factor of 2 increase in comparison with the native, undoped ones. The ultrafast transient absorption and time-resolved photoluminescence (PL) spectroscopy revealed that Ce 3+ -doping can significantly modulate the PL kinetics to enhance the PL efficiency of doped CsPbBr 3 NCs. As a result, the LED device fabricated by adopting Ce 3+ -doped CsPbBr 3 NCs as the emitting layers exhibited a pronounced improvement of electroluminescence with external quantum efficiency (EQE) from 1.6 to 4.4% via Ce 3+ -doping.

Enhanced T{sub c} in a dual-layered molecular superconductor

Energy Technology Data Exchange (ETDEWEB)

Souza, Mariano de; Lang, Michael [Physikalisches Institut, J.W. Goethe-Universitaet, SFB/TR49, D-60438 Frankfurt/M (Germany); Wiehl, Leonor [Institut fuer Geowissenschaften, J.W. Goethe-Universitaet, D-60438 Frankfurt/M (Germany); Schlueter, John A. [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439 (United States)

2011-07-01

We have revisited the structural and electronic properties of the filamentary organic superconductor (BEDT-TTF){sub 2}Ag(CF{sub 3}){sub 4}(TCE), first synthesized in 1994. Detailed structural investigations reveal that the BEDT-TTF molecules are arranged in two distinctly different packing motifs, {kappa} and {alpha}', which alternate from layer to layer. This molecule-based superconductor with dual BEDT-TTF packing motifs has a T{sub c} five times higher than that of its polymorph that contains only {kappa}-type packing. Using the established empirical correlations between the bond lengths (C-S and C=S) and the oxidation state of the BEDT-TTF molecule, we have found that there is a uniform charge distribution in the {kappa}-layers (corresponding to an oxidation state of +0.5 for all BEDT-TTF molecules), whereas in the {alpha}'-layer, half of the molecules are nearly fully oxidized to +1, while the other half are close to neutral, resulting in a charge-ordered neutral layer. These findings indicate that this material can be considered as a promising candidate for a distinctly two-dimensional superconductor.

Crystal structures of MBi{sub 2}Br{sub 7} (M = Rb, Cs) - filled variants of AX{sub 7} sphere packing

Energy Technology Data Exchange (ETDEWEB)

Chang, Jen-Hui; Wolff, Alexander [Fachrichtung Chemie und Lebensmittelchemie, Technische Universitaet Dresden, 01062 Dresden (Germany); Ruck, Michael [Fachrichtung Chemie und Lebensmittelchemie, Technische Universitaet Dresden, 01062 Dresden (Germany); Max-Planck-Institut fuer Chemische Physik fester Stoffe, Noethnitzer Str. 40, 01187 Dresden (Germany)

2016-03-15

The reinvestigation of the pseudo-binary systems MBr-BiBr{sub 3} (M = Rb, Cs) revealed two new phases with composition MBi{sub 2}Br{sub 7}. Both compounds are hygroscopic and show brilliant yellow color. The crystal structures were solved from X-ray single crystal diffraction data. The isostructural compounds adopt a new structure type in the triclinic space group P anti 1. The lattice parameters are a = 755.68(3) pm, b = 952.56(3) pm, c = 1044.00(4) pm, α = 76.400(2) , β = 84.590(2) , γ = 76.652(2) for RbBi{sub 2}Br{sub 7} and a = 758.71(5) pm, b = 958.23(7) pm, c = 1060.24(7) pm, α = 76.194(3) , β = 83.844(4) , γ = 76.338(3) for CsBi{sub 2}Br{sub 7}. The crystal structures consist of M{sup +} cations in anticuboctahedral coordination by bromide ions and bromidobismuthate(III) layers {sup 2}{sub ∞}[Bi{sub 2}Br{sub 7}]{sup -}. The 2D layers comprise pairs of BiBr{sub 6} octahedra sharing a common edge. The Bi{sub 2}Br{sub 10} double octahedra are further connected by common vertices. The bismuth(III) atoms increase their mutual distance in the double octahedra by off-centering so that the BiBr{sub 6} octahedra are distorted. The CsBi{sub 2}Br{sub 7} type can be interpreted as a common hexagonal close sphere packing of M and Br atoms, in which 1/4 of the octahedral voids are filled by Bi atoms. The structure type was systematically analyzed and compared with alternative types of common packings. The existence of a compound with the suggested composition CsBiBr{sub 4} could not be verified experimentally. (Copyright copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Fabrication of the heterostructured CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} hybrid photocatalyst with enhanced performance of photocatalytic hydrogen production from water

Energy Technology Data Exchange (ETDEWEB)

Lang, Junyu; Liu, Mengqing; Su, Yiguo; Yan, Lijuan; Wang, Xiaojing, E-mail: wang_xiao_jing@hotmail.com

2015-12-15

Graphical abstract: - Highlights: • A novel ternary CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} hybrid photocatalyst was successfully fabricated. • Au particles act as an electron-conduction bridge between the heterostructure. • The photoctalytic hydrogen generation was promoted by the SPR of the Au. • CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} shows significant photocatalytic activity in H{sub 2} generation. - Abstract: In this work, a novel CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} hybrid photocatalyst is successfully fabricated. The photocatalytic performance of the heterostructured CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} composite was investigated. Au nanoparticles were photo-deposited as the interlayer between g-C{sub 3}N{sub 4} and the surface of CsTaWO{sub 6}, which can facilitate the photoinduced electrons migration as an electron-conduction bridge as well as increase visible-light absorption via the surface plasmon resonance. This heterostructured interface bridging by Au particles may significantly retard the recombination of electron–holes, which is beneficial to promote the photocatalytic activity under visible-light irradiation. It is found the CsTaWO{sub 6}/Au/g-C{sub 3}N{sub 4} sample showed excellent photocatalytic activity of water splitting, even higher than the sum of g-C{sub 3}N{sub 4} and Au/CsTaWO{sub 6} samples, or the sum of CsTaWO{sub 6} and Au/g-C{sub 3}N{sub 4} samples. It indicates that the heterostructured combination of g-C{sub 3}N{sub 4} and CsTaWO{sub 6} bridging by Au particles provided the synergistic photocatalytic activity driving by solar light through an efficient electron transfer process.

Accumulation and distribution of 137Cs in the organic matter of soil during decomposition of forest dead leaves

International Nuclear Information System (INIS)

Jokhanson, K.J.; Dolgilevich, M.I.

2000-01-01

The samples of dead leaves, litter, and soil were taken in 1996 in the forest area located in the Ovruch district of the Zhytomyr region, Ukraine and where ground depositions of 137 Cs range from 100 to 590 kBq/m 2 . Radiocaesium activity of all organic fractions of litter decreased in comparison with radioactivity of the same fractions of dead leaves. Only hydrochloric acid hydrolysate of hemicellulose had a very big radioactivity reached 12-32% of radioactivity of samples. Apparently, hydrochloric acid extracted exchangeable 137 Cs (11-17%) and joined one with mineral substances. Organic matter content in the soil layer at a depth of 6-12 cm was 3,4%, the main organic fraction components were residues after hydrolysis and humus substances extracted by sodium pyrophosphate - 52.2 and 28.8%, respectively. In the same soil layer, radiocaesium activity was 0.63 kBg/kg

Differential leaching of 137Cs from sediment core depth fractions of Bombay harbour bay

International Nuclear Information System (INIS)

Hemalatha, P.; Desai, M.V.M.

1998-01-01

Bombay harbour bay receives 137 Cs from the effluents of research reactors, fuel reprocessing plant and isotope laboratories. 137 Cs is strongly taken up by suspended particulates and sediments and is trapped in the layer lattices of the clay minerals. As the siltation rate is high in the bay, 137 Cs gets distributed vertically along the depth of sediment. NaCl solution has been proved to desorb 137 Cs from clay minerals effectively. NaCl solution of ionic strength 1.6 was used to desorb 137 Cs from depth fractions of a sediment core to obtain a possible gradient of leaching with the depth. A definite rate of leaching was observed for the 137 Cs in the core sediment depth fractions. About 13% to 56% of 137 Cs was leached. As the depth increases removal rate of cesium decreases. This is expected to bring out a relation between age of 137 Cs and rate of its leaching. (author)

Particle identification method in the CsI(Tl) scintillator used for the CHIMERA 4 pi detector

CERN Document Server

Alderighi, M; Basssini, R; Berceanu, I; Blicharska, J; Boiano, C; Borderie, B; Bougault, R; Bruno, M; Cali, C; Cardella, G; Cavallaro, S; D'Agostino, M; D'andrea, M; Dayras, R; De Filippo, E; Fichera, F; Geraci, E; Giustolisi, F; Grzeszczuk, A; Guardone, N; Guazzoni, P; Guinet, D; Iacono-Manno, M; Kowalski, S; La Guidara, E; Lanchais, A L; Lanzalone, G; Lanzanò, G; Le Neindre, N; Li, S; Maiolino, C; Majka, Z; Manfredi, G; Nicotra, D; Paduszynski, T; Pagano, A; Papa, M; Petrovici, C M; Piasecki, E; Pirrone, S; Politi, G; Pop, A; Porto, F; Rivet, M F; Rosato, E; Sacca, G; Sechi, G; Simion, V; Sperduto, M L; Steckmeyer, J C; Trifiró, A; Trimarchi, M; Urso, S; Vannini, G; Vigilante, M; Wilczynski, J; Wu, H; Xiao, Z; Zetta, L; Zipper, W

2002-01-01

The charged particle identification obtained by the analysis of signals coming from the CsI(Tl) detectors of the CHIMERA 4 pi heavy-ion detector is presented. A simple double-gate integration method, with the use of the cyclotron radiofrequency as reference time, results in low thresholds for isotopic particle identification. The dependence of the identification quality on the gate generation timing is discussed. Isotopic identification of light ions up to Beryllium is clearly seen. For the first time also the identification of Z=5 particles is observed. The identification of neutrons interacting with CsI(Tl) by (n,alpha) and (n,gamma) reactions is also discussed.

Early stages of Cs adsorption mechanism for GaAs nanowire surface

Science.gov (United States)

Diao, Yu; Liu, Lei; Xia, Sihao; Feng, Shu

2018-03-01

In this study, the adsorption mechanism of Cs adatoms on the (100) surface of GaAs nanowire with [0001] growth direction is investigated utilizing first principles method based on density function theory. The adsorption energy, work function, atomic structure and electronic property of clean surface and Cs-covered surfaces with different coverage are discussed. Results show that when only one Cs is adsorbed on the surface, the most favorable adsorption site is BGa-As. With increasing Cs coverage, work function gradually decreases and gets its minimum at 0.75 ML, then rises slightly when Cs coverage comes to 1 ML, indicating the existence of 'Cs-kill' phenomenon. According to further analysis, Cs activation process can effectively reduce the work function due to the formation of a downward band bending region and surface dipole moment directing from Cs adatom to the surface. As Cs coverage increases, the conduction band minimum and valence band maximum both shift towards lower energy side, contributed by the orbital hybridization between Cs-5s, Cs-5p states and Ga-4p, As-4s, As-4p states near Fermi level. The theoretical calculations and analysis in this study can improve the Cs activation technology for negative electron affinity optoelectronic devices based on GaAs nanowires, and also provide a reference for the further Cs/O or Cs/NF3 activation process.

Formation of 2D-PhCs with missing holes based on Si-layers by EBL

Science.gov (United States)

Utkin, D. E.; Shklyev, A. A.; Tsarev, A. V.; Latyshev, A. V.

2017-11-01

The fabrication of the periodic structures, that is two-dimensional photonic crystals (2D PhCs) based on Si-materials by electron beam lithography (EBL) technique has been studied. We have investigated basic lithography processes such as designing, exposition, development, etching and others. The developed top-down approach allows close-packed arrays of elements and holes to be formed in nanometre range. This can be used to produce 2D PhCs with emitting micro-cavities (missing holes) with lateral size parameters with an accuracy of about 2% in the Si (100) substrate and in silicon-on-insulator structures. Such accuracy is expected to be sufficient for obtaining the cavities-coupling radiation interference from large areas of 2D PhCs.

Thermodynamics of the amalgam cells {l_brace}Cs-amalgam|CsX (m)|AgX|Ag{r_brace} (X=Cl, Br, I) and primary medium effects in (methanol+water) (acetonitrile+water), and (1,4-dioxane+water) solvent mixtures

Energy Technology Data Exchange (ETDEWEB)

Falciola, Luigi [Department of Physical Chemistry and Electrochemistry, University of Milan, Via Golgi 19, I-20133 Milan (Italy)]. E-mail: luigi.falciola@unimi.it; Longoni, Giorgio [Department of Physical Chemistry and Electrochemistry, University of Milan, Via Golgi 19, I-20133 Milan (Italy); Mussini, Patrizia R. [Department of Physical Chemistry and Electrochemistry, University of Milan, Via Golgi 19, I-20133 Milan (Italy)]. E-mail: patrizia.mussini@unimi.it; Mussini, Torquato [Department of Physical Chemistry and Electrochemistry, University of Milan, Via Golgi 19, I-20133 Milan (Italy)]. E-mail: torquato.mussini@unimi.it

2006-06-15

The potential difference E of the amalgam cell {l_brace}Cs{sub x}Hg{sub 1-x}|CsX (m)|AgX|Ag{r_brace} (X=Cl, Br, I) has been measured as a function of the mole fraction x{sub Cs} of Cs metal in amalgams and of the molality m of CsX in (methanol+water) (acetonitrile+water), and (1,4-dioxane+water) solvent mixtures containing up to 0.75 mass fraction of the organic component, at the temperature 298.15K. The respective standard molal potential differences E{sub m}{sup o} have been determined together with the relevant activity coefficients {gamma}{sub +}/- as functions of the CsX molality. The found E{sub m}{sup o} values show a parabolic decrease with increasing proportion of the organic component in the solvent mixture. Analysis of the relevant primary medium effects upon CsX shows that the CsX transfer from the standard state in water to the standard state in the (aqueous+organic) mixture is always unfavoured, and the acetonitrile is the least unfavoured co-solvent studied. Analysis of the primary medium effect upon CsI in terms of Feakins and French's theory leads to a primary hydration number close to zero, which is consistent with the results of supplementary EXAFS experiments on Cs{sup +} and I{sup -} in (acetonitrile+water) solvent mixtures.

Distribution of 90Sr and 137Cs in Arctic soil profiles polluted by heavy metals

International Nuclear Information System (INIS)

Puhakainen, M.; Heikkinen, T.; Steinnes, E.; Thorring, H.; Outola, I.

2005-01-01

Effects of industrial pollution on the behaviour of radionuclides in spruce forest ecosystems were studied along a gradient from of a copper-nickel smelter in Monchegorsk, NW Russia. A reference site was situated in Lapland, Finland, 152 km west of Monchegorsk. Most of the total 137 Cs activity in soil was in mineral (E and B) horizons, except at the reference site where the major part was still in the organic surface layer. Most of the total 90 Sr activity still remaining in the soil profile was found in the surface layer, but the relative amount decreased with increasing level of industrial pollution. Pollutants from the smelter clearly affected the chemical speciation of radionuclides. Smaller amounts of exchangeable radionuclides were present in the organic surface layer at the most polluted sites. The decline of 137 Cs with decreasing distance from the smelter correlated strongly with a similar depletion in exchangeable K and Mg. Total concentrations of 137 Cs and 90 Sr showed high correlations with exchangeable cations, particularly in the E and upper B horizon. A sudden change in behaviour of 137 Cs in the lower B horizon may be associated with changes in clay mineralogy along the soil profile caused by weathering

Optimising the measurement of bruises in children across conventional and cross polarized images using segmentation analysis techniques in Image J, Photoshop and circle diameter measurements.

Science.gov (United States)

Harris, C; Alcock, A; Trefan, L; Nuttall, D; Evans, S T; Maguire, S; Kemp, A M

2018-02-01

Bruising is a common abusive injury in children, and it is standard practice to image and measure them, yet there is no current standard for measuring bruise size consistently. We aim to identify the optimal method of measuring photographic images of bruises, including computerised measurement techniques. 24 children aged Photoshop 'ruler' software (Photoshop diameter)). Inter and intra-observer effects were determined by two individuals repeating 11 electronic measurements, and relevant Intraclass Correlation Coefficient's (ICC's) were used to establish reliability. Spearman's rank correlation was used to compare in vivo with computerised measurements; a comparison of measurement techniques across imaging modalities was conducted using Kolmogorov-Smirnov tests. Significance was set at p 0.5 for all techniques, with maximum Feret diameter and maximum Photoshop diameter on conventional images having the strongest correlation with in vivo measurements. There were significant differences between in vivo and computer-aided measurements, but none between different computer-aided measurement techniques. Overall, computer aided measurements appeared larger than in vivo. Inter- and intra-observer agreement was high for all maximum diameter measurements (ICC's > 0.7). Whilst there are minimal differences between measurements of images obtained, the most consistent results were obtained when conventional images, segmented by Image J Software, were measured with a Feret diameter. This is therefore proposed as a standard for future research, and forensic practice, with the proviso that all computer aided measurements appear larger than in vivo. Copyright © 2018 Elsevier Ltd and Faculty of Forensic and Legal Medicine. All rights reserved.

Analysis on the influence of forest soil characteristics on radioactive Cs infiltration and evaluation of residual radioactive Cs on surfaces.

Science.gov (United States)

Mori, Yoshitomo; Yoneda, Minoru; Shimada, Yoko; Fukutani, Satoshi; Ikegami, Maiko; Shimomura, Ryohei

2018-03-29

We investigated the depth profiles of radioactive Cs, ignition loss, and cation exchange capacity (CEC) in five types of forest soils sampled using scraper plates. We then simulated the monitored depth profiles in a compartment model, taking ignition loss as a parameter based on experimental results showing a positive correlation between ignition loss and the CEC. The calculated values were comparable with the monitored values, though some discrepancy was observed in the middle of the soil layer. Based on decontamination data on the surface dose rate and surface contamination concentration, we newly defined a surface residual index (SRI) to evaluate the residual radioactive Cs on surfaces. The SRI value tended to gradually decrease in forests and unpaved roads and was much smaller in forests and on unpaved roads than on paved roads. The radioactive Cs was assumed to have already infiltrated underground 18 months after the nuclear power plant accident, and the sinking was assumed to be ongoing. The SRI values measured on paved roads suggested that radioactive Cs remained on the surfaces, though a gradual infiltration was observed towards the end of the monitoring term. The SRI value is thought to be effective in grasping the rough condition of residual radioactive Cs quickly at sites of decontamination activity in the field. The SRI value may be serviceable for actual contamination works after further research is done to elucidate points such as the relation between the SRI and the infiltration of radioactive Cs in various types of objects.

Protonic Conductors for Intermediate Temperature Fuel Cell Electrolytes: Superprotonic CsH2PO4 Stabilization and in-Doped SnP2O7 Structure Study

Science.gov (United States)

Martinez Salinas, Heber Jair

Proton conductor solid electrolytes CsH2PO4 and In-doped tin pyrophosphate have been investigated as candidates to fill a gap of suitable electrolytes for fuel cells at the intermediate temperature range due their unusually high conductivities between 200 and 300 °C. Unfortunately, in the case of CsH2PO4, complicated experimental conditions, like a humidified environment, or high pressure, are needed to preserve the sought high conducting phase. In the first stage of this work, X-ray diffraction on CsH2PO 4 samples performed in air, and under normal conditions of humidity and pressure, evidence of the cubic phase of CsH2PO4 was observed during short intervals of temperature and time, starting at 215 °C and disappearing completely at 265 °C into a dehydrated phase. An AC impedance spectroscopy experimental setup has been assembled and data has been successfully collected on undoped, and doped CsH2PO 4 samples to investigate the effects of chemical and environmental modifications. Measurements performed in the temperature range 200 - 260 °C, and using the frequency range 1 - 6 MHz, showed that the high conducting phase of undoped CsH2PO4 was present for a very short interval of temperature. Additionally, these measurements showed that nano-silica-doped CsH2PO4, and CsH2PO4 under a humidified environment achieve the highest values of conductivity, above 10-2 S cm-1 among the samples tested. In the second stage of this investigation, AC impedance spectroscopy measurements were successfully performed on CsH2PO4 samples in air, at temperatures from 200 - 260 °C, and in the frequency range 1 - 6 MHz, inside a hermetically sealed stainless-steel chamber, which was designed and assembled in-house. Results showed that the highly conducting phase of CsH2PO 4 was achieved at temperatures measured above 230 °C, reaching conductivity values up to 1.7 x10-2 S cm-1, and remaining stable for over 40 hours. Consequent X-ray diffraction analysis of such samples showed that a

Long term behaviour and seasonal cycling of Cs-137 in a eutrophic lake in Southern Germany

Energy Technology Data Exchange (ETDEWEB)

Klemt, E.; Knaus, J.; Putyrskaya, V.; Ries, T. [Hochschule Ravensburg-Weingarten (Germany)

2014-07-01

Lake Vorsee is a small and shallow eutrophic lake with a swampy watershed about 25 km north of Lake Constance in southern Germany which is intensely used for fishing by local fishermen. It is completely overgrown by watermilfoil (Myriophyllum spicatum) which produces thick watery organic sediment layers when it decomposes in late autumn and winter. In 1986 the watershed of Lake Vorsee had a Cs-137 Chernobyl inventory of about 30 kBq/m{sup 2}. The Cs-137 activity concentration in the water was monitored for more than 25 years and it can be well described by a sum of two exponential functions superimposed by some seasonal cycling. To analyze the seasonal cycling of the Cs-137 activity concentration in water and in suspended matter, samples were collected with a Large Volume Water Sampler (Midiya-System) on a monthly base and measured gamma-spectrometrically by HPGe-detectors. Also the Cs-137 distribution coefficient kD was determined. Additionally, in the lake water the concentration of the competing ions K{sup +} and NH{sub 4}{sup +} was determined by ion-chromatography, total organic carbon (TOC) with a combustion catalytic oxidation / NDIR detection method as well as the dissolved O{sub 2}-concentration and the pH and temperature of the water by hand-held probes. Information on the amount of precipitation was taken from nearby weather stations. In this project the following hypothesis will be checked: In late autumn the decomposing watermilfoil produces NH{sub 4}{sup +}-ions which exchange Cs{sup +}-ions from their binding places, thereby increasing the Cs-137 activity concentration in the water. In spring the watermilfoil starts growing which leads to a larger O{sub 2}-concentration in the water and helps to disintegrate the NH{sub 4}{sup +}-ions in this way decreasing the Cs-137 concentration again. A possible influence of the other measured parameters on the seasonal cycling will also be discussed. Document available in abstract form only. (authors)

Activation energies of diffusion for I and Cs in interlayer of smectite

International Nuclear Information System (INIS)

Sato, H.

2009-01-01

The apparent diffusivities (Da) and activation energies (ΔEa) for I - and Cs + ions in compacted Na-smectite with an interlayer space of only 2 water layers were measured at a dry density of 1.79 Mg/m 3 . In-diffusion experiments were carried out under the conditions that interlayer space, orientation of smectite stacks and dry density were controlled. Basal spacing was checked by X-ray diffractometry (XRD). All diffraction peaks to d(001) indicated basal spacing, of which interlayer space was equal to 2 water layers. The ΔEa of I - ions was at similar level as that for the ionic diffusivity of I - ions in free water (Do) at a dry density of 1.0 Mg/m 3 , but was 35.24 kJ/mol at a dry density of 1.79 Mg/m 3 . The ΔEa for Cs + ions was 46.27 kJ/mol which was higher than that for I? ions, at a dry density of 1.79 Mg/m 3 . Such high ΔEa for I - ions in the interlayer of smectite could be explained by the lowering in the activity (a H 2 O ) of interlayer water. Since Cs + ions sorb onto smectite by ion exchange, such high ΔEa for Cs + ions could be explained by the combined effects of the Cs+/Na+ ion exchange enthalpy (ΔH o ) in smectite and the lowering in the a H 2 O of interlayer water. (author)

Soil 137Cs background values in monsoon region of china

International Nuclear Information System (INIS)

Zhang Mingli; Yang Hao; Wang Xiaolei; Wang Yihong; Xu Congan; Yang Jiudong; Rong Jing

2009-01-01

Land degradation,, which is resulted from the soil erosion, is one of the major environmental problems. It severely affects the food supplies, environmental safety and the sustainable development in China. Some areas in the monsoon region are suffering from the acute soil erosion. To find out the degree of soil erosion, the proven technique of 137 Cs tracer is definitely one of the best methods, and the key is to ascertain the accuracy of soil 137 Cs background value. The distributions of 137 Cs were explored in soil profiles by detecting the 137 Cs of soil cores from the Yimeng mountain area in Shandong Province, hills in the southern area of Jiangsu Province and Dianchi catchment in Yunnan Province, respectively. We found that the depth of 137 Cs distribution is not the same in the soils of various areas. But the 137 Cs activity shows an exponential distribution in the uncultivated soil and demonstrates a strong correlation with the soil depth, while the 137 Cs activity proves uniform in the soil plowing layer of the cultivated land. The study shows the 137 Cs background values of three areas: 1737.1 Bq/m 2 in Yimeng mountain area, 1847.6 Bq/m 2 in southern area of hills in Jiangsu, 918.0 Bq/m 2 in Dianchi catchment. The certainty of 137 Cs background value can technically support the use of 137 Cs technique to study the spatial pattern of soil erosion, deposition and the land degradation, which provides the support for the sustainable utilization of soil resource, the assessment of economical benefit and loss and the evaluation of water and soil conservation measures. (authors)

Analysis on the influence of forest soil characteristics on radioactive Cs infiltration

International Nuclear Information System (INIS)

Mori, Yoshitomo; Yoneda, Minoru; Shimada, Yoko; Shimomura, Ryohei; Fukutani, Satoshi; Ikegami, Maiko

2017-01-01

Soil core (0-5 cm and 5-10 cm) was collected in 5 points with different vegetation in Fukushima Prefecture in order to explore the permeability, field capacity and voidage. Depth profiles of radioactive Cs, ignition loss and CEC (Cation Exchange Capacity) in the 5 forest soils were also investigated, using scraper plate (at 0.5 cm intervals for 0-5 cm and at 1.0 cm intervals for 5-10 cm). Depth profiles in soil layers were totally different between forests and did not show explicit correlation with field capacity, voidage or ignition loss. On the other hand, CEC correlated weakly and permeability did strongly with infiltration of radioactive Cs. Compartment modeling was conducted, so as to reproduce the monitored depth profile, taking ignition loss as a parameter, based on the experiment result that ignition loss had positive correlation with CEC, which might influence the adsorption process on radioactive Cs in soil layer. However, the ignition loss alone failed to fully reproduce the depth profile. Considering the present results as well as the fact that permeability might have explicit relation with infiltration of radioactive Cs, factors related with precipitation or water flow in early stage after the accident could influence the depth profile, before adsorbed with negative charge in soil particles. (author)

Experimental and computation method for determination of burnup and isotopic composition of the WWER-440 fuel using the 134Cs and 137Cs concentrations

International Nuclear Information System (INIS)

Babichev, B.A.; Kozharin, V.V.

1990-01-01

An experimental and computational method for determination of burnup and actinoid concentrations in WWER fuel elements using 134 Cs and 137 Cs concentrations in fuel is considered. It is shown that the error in calculation of fuel burnup and U and Pu isotope concentrations in WWER-440 fuel elements is 1.3-4.9% provided that the error in 134 Cs and 137 Cs concentration measurements does not exceed 1.7 and 1.2%. 9 refs.; 10 figs.; 4 tabs

A Monte Carlo study of backscattering effects in the photoelectron emission from CsI into CH$_{4}$ and Ar-CH$_{4}$ mixtures

CERN Document Server

Escada, J; Rachinhas, P J B M; Lopes, J A M; Santos, F P; Távora, L M N; Conde, C A N; Stauffer, A D

2007-01-01

Monte Carlo simulation is used to investigate photoelectron backscattering effects in the emission from a CsI photocathode into CH4 and Ar-CH4 mixtures for incident monochromatic photons with energies Eph in the range 6.8 eV to 9.8 eV (182 nm to 127 nm), and photons from a continuous VUV Hg(Ar) lamp with a spectral distribution peaked at Eph = 6.7 eV (185 nm), considering reduced applied electric fields E/N in the 0.1 Td to 40 Td range. The addition of CH4 to a noble gas efficiently increases electron transmission and drift velocity, due to vibrational excitation of the molecules at low electron energies. Results are presented for the photoelectron transmission efficiencies f, where f is the fraction of the number of photoelectrons emitted from CsI which are transmitted through the gas as compared to vacuum. The dependence of f on Eph, E/N, and mixture composition is analyzed and explained in terms of electron scattering in the different gas media, and results are compared with available measurements. Electro...

Degradation of 4-Chloro phenol by gamma radiation of 137Cs and X-rays

International Nuclear Information System (INIS)

Gonzalez J, J. C.; Jimenez B, J.; Cejudo A, J.

2010-01-01

This paper presents results of radiolytic degradation of 4-chloro phenol in the presence of TiO 2 , Al 2 O 3 and SiO 2 , using different radiation sources than 60 Co, which is so common in this type of experiment. The radiation sources used were X-rays with energy of 100 keV and radiation from 137 Cs (662 keV). After irradiation with a dose of 50 c Gy X-ray and TiO 2 obtained a degradation of about 5%, no degradation was obtained with 137 Cs source and other oxides. This may be due to the fact that X-rays have a linear energy transfer greater value, and in the case of TiO 2 present a crystalline structure, whereas the other two oxides are amorphous. Both characteristics result in better formation of a reactive species that allows the degradation of the compound. (Author)

MENINGKATKAN KEMAMPUAN KOMUNIKASI DAN PENALARAN SERTA DISPOSISI MATEMATIK SISWA SMK DENGAN PENDEKATAN KONTEKSTUAL MELALUI GAME ADOBE FLASH CS 4.0

Directory of Open Access Journals (Sweden)

Martin Bernard

2015-07-01

Full Text Available ABSTRAK Penelitian ini bertujuan untuk menelaah pencapaian dan peningkatan kemampuan komunikasi dan penalaran matematik siswa yang pembelajaran dengan pendekatan kontekstual melalui game Adobe Flash CS 4.0 lebih baik daripada pembelajaran kontekstual dengan cara biasa, menalaah asosiasi kemampuan komunikasi dan penalaran matematika siswa, asosiasi skala disposisi dan kemampuan komunikasi dan asosiasi skala disposisi dan kemampuan penalaran. Serta bagaimana menelaah kemampuan komunikasi dan penalaran matematik siswa terhadap pendekatan pembelajaran. Metode penelitian yang dipakai adalah menggunakan kuasi eksperimen. Dimana metode ini terdiri dua kelas, bahwa kelas pertama diberi perlakuan yaitu kelas yang pembelajaran pendekatan kontekstual menggunakan game Adobe Flash CS 4.0 dan kelas yang kedua yaitu kelas yang pembelajaran pendekatan kontekstual dengan cara biasa. Populasi yang diambil di sekolah SMK Mahardika dan sampelnya adalah 40 siswa kelas X.1 sebagai kelas Kontrol dan 42 siswa kelas X.2 sebagai kelas Eksperimen. Instrumen yang digunakan berupa 10 butir soal diantaranya 5 soal kemampuan komunikasi dan 5 soal kemampuan penalaran berbentuk uraian yang telah diuji validitas, realibilitas, derajat pembeda dan indeks kesukaran. Untuk angket skala disposisi yang digunakan adalah angket skala Linkert yang berbentuk ordinal yang akan dikonversi ke bentuk interval melalui Method Seccessive Interval (MSI. Kesimpulan dari penelitian tersebut yaitu pencapaian dan peningkatan kemampuan komunikasi dan penalaran serta disposisi matematik siswa dengan pendekatan kontekstual melalui Game Adobe Flash CS 4.0 lebih baik dibandingkan dengan pembelajaran cara biasa, adanya asosiasi antara kemampuan komunikasi dan penalaran tetapi tidak ada asosiasi antara disposisi dengan kemampuan komunikasi dan penalaran.   Kata Kunci    :   Komunikasi, Penalaran, Skala Disposisi, Pendekatan Kontekstual, Adobe Flash CS 4     ABSTRACT This study aimed to examine the

Effect of moisture and chitosan layered silicate on morphology and properties of chitosan/layered silicates films

International Nuclear Information System (INIS)

Silva, J.R.M.B. da; Santos, B.F.F. dos; Leite, I.F.

2014-01-01

Thin chitosan films have been for some time an object of practical assessments. However, to obtain biopolymers capable of competing with common polymers a significant improvement in their properties is required. Currently, the technology of obtaining polymer/layered silicates nanocomposites has proven to be a good alternative. This work aims to evaluate the effect of chitosan content (CS) and layered silicates (AN) on the morphology and properties of chitosan/ layered silicate films. CS/AN bionanocomposites were prepared by the intercalation by solution in the proportion 1:1 and 5:1. Then were characterized by infrared spectroscopy (FTIR), diffraction (XRD) and X-ray thermogravimetry (TG). It is expected from the acquisition of films, based on different levels of chitosan and layered silicates, choose the best composition to serve as a matrix for packaging drugs and thus be used for future research. (author)

GrinLine identification using digital imaging and Adobe Photoshop.

Science.gov (United States)

Bollinger, Susan A; Brumit, Paula C; Schrader, Bruce A; Senn, David R

2009-03-01

The purpose of this study was to outline a method by which an antemortem photograph of a victim can be critically compared with a postmortem photograph in an effort to facilitate the identification process. Ten subjects, between 27 and 55 years old provided historical pictures of themselves exhibiting a broad smile showing anterior teeth to some extent (a grin). These photos were termed "antemortem" for the purpose of the study. A digital camera was used to take a current photo of each subject's grin. These photos represented the "postmortem" images. A single subject's "postmortem" photo set was randomly selected to be the "unknown victim." These combined data of the unknown and the 10 antemortem subjects were digitally stored and, using Adobe Photoshop software, the images were sized and oriented for comparative analysis. The goal was to devise a technique that could facilitate the accurate determination of which "antemortem" subject was the "unknown." The generation of antemortem digital overlays of the teeth visible in a grin and the comparison of those overlays to the images of the postmortem dentition is the foundation of the technique. The comparisons made using the GrinLine Identification Technique may assist medical examiners and coroners in making identifications or exclusions.

Rietveld refinement of the orthorhombic Pbca structures of Rb2CdSi5O12, Cs2MnSiO5O12, Cs2CoSi5O12 and Cs2NiSi5O12 leucites by synchrotron X-ray powder diffraction

International Nuclear Information System (INIS)

Bell, A.M.T.; Henderson, C.M.B.

1996-01-01

Analysis of high-resolution synchrotron X-ray powder diffraction patterns for hydrothermally synthesized Rb 2 CdSi 5 O 12 and Cs 2 MnSi 5 O 12 leucite analogues, and dry-synthesized Cs 2 CoSi 5 O 12 and Cs 2 NiSi 5 O 12 leucite analogues showed that they have an orthorhombic Pbca structure. The structures have been refined by the Rietveld method, showing that the tetrahedrally coordinated atoms (Si, Cd, Mn, Co and Ni) are ordered on separate sites. The Cs 2 MnSi 5 O 12 , Cs 2 CoSi 5 O 12 and Cs 2 NiSi 5 O 12 leucite samples are unusual in containing SiO 4 tetrahedra which are more distorted, on average, than the larger MnO 4 , CoO 4 and NiO 4 tetrahedra. The JCPDS file numbers for Rb 2 CdSi 5 O 12 , Cs 2 MnSi 5 O 12 and Cs 2 CoSi 5 O 12 are 46-1491, 46-1492 and 46-1493, respectively. (orig.)

Thin layer chitosan-coated cellulose filter paper as substrate for immobilization of catalytic cobalt nanoparticles.

Science.gov (United States)

Kamal, Tahseen; Khan, Sher Bahadar; Haider, Sajjad; Alghamdi, Yousef Gamaan; Asiri, Abdullah M

2017-11-01

A facile approach utilizing synthesis of cobalt nanoparticles in green polymers of chitosan (CS) coating layer on high surface area cellulose microfibers of filter paper (CFP) is described for the catalytic reduction of nitrophenol and an organic dye using NaBH 4 . Simple steps of CFP coating with 1wt% CS aqueous solution followed by Co 2+ ions adsorption from 0.2M CoCl 2 aqueous solution were carried out to prepare pre-catalytic strips. The Co 2+ loaded pre-catalytic strips of CS-CFP were treated with 0.19M NaBH 4 aqueous solution to convert the ions into nanoparticles. Successful Co nanoparticles formation was assessed by various characterization techniques of FESEM, EDX and XRD analyzes. TGA analyses were carried out on CFP, CS-CFP, and Co-CS-CFP for the determination of the amount of Co particles formed on the CS-FP, and to track their thermal properties. Furthermore, we demonstrated that the Co-CS-CFP showed an excellent catalytic activity and reusability in the reduction reactions a nitroaromatic compound of 2,6-dintirophenol (2,6-DNP) and brilliant cresyl blue (BCB) dye by NaBH 4 . The Co-CS-CFP catalyzed the reduction reactions of 2,6-DNP and BCB by NaBH 4 with psuedo-first order rate constants of 0.0451 and 0.1987min -1 , respectively. Copyright © 2017 Elsevier B.V. All rights reserved.

Correlations between potassium, rubidium and cesium (133Cs and 137Cs) in sporocarps of Suillus variegatus in a Swedish boreal forest

International Nuclear Information System (INIS)

Vinichuk, M.; Rosen, K.; Johanson, K.J.; Dahlberg, A.

2011-01-01

An analysis of sporocarps of ectomycorrhizal fungi Suillus variegatus assessed whether cesium ( 133 Cs and 137 Cs) uptake was correlated with potassium (K) or rubidium (Rb) uptake. The question was whether intraspecific correlations of Rb, K and 133 Cs mass concentrations with 137 Cs activity concentrations in sporocarps were higher within, rather than among, different fungal species, and if genotypic origin of sporocarps within a population affected uptake and correlation. Sporocarps (n = 51) from a Swedish forest population affected by the fallout after the Chernobyl accident were studied. The concentrations were 31.9 ± 6.79 g kg -1 for K (mean ± SD, dwt), 0.40 ± 0.09 g kg -1 for Rb, 8.7 ± 4.36 mg kg -1 for 133 Cs and 63.7 ± 24.2 kBq kg -1 for 137 Cs. The mass concentrations of 133 Cs correlated with 137 Cs activity concentrations (r = 0.61). There was correlation between both 133 Cs concentrations (r = 0.75) and 137 Cs activity concentrations (r = 0.44) and Rb, but the 137 Cs/ 133 Cs isotopic ratio negatively correlated with Rb concentration. Concentrations of K and Rb were weakly correlated (r = 0.51). The 133 Cs mass concentrations, 137 Cs activity concentrations and 137 Cs/ 133 Cs isotopic ratios did not correlate with K concentrations. No differences between, within or, among genotypes in S. variegatus were found. This suggested the relationships between K, Rb, 133 Cs and 137 Cs in sporocarps of S. variegatus is similar to other fungal species. - Highlights: → We studied uptake of Cs ( 133 Cs and 137 Cs), K and Rb by Suillus variegates sporocarps. → Genotypic origin of fungus did not affect uptake of studied elements (isotopes). → Genotypic origin did not affect correlation between Cs ( 133 Cs and 137 Cs), K and Rb.

Distribution of 137Cs in samples of ocean bottom sediments of the baltic sea in 1982-1983

International Nuclear Information System (INIS)

Gedenov, L.I.; Flegontov, V.M.; Ivanova, L.M.; Kostandov, K.A.

1986-01-01

The concentration of Cs-137 in samples of ocean bottom sediments picked up in 1979 in the Gulf of Finland with a geological nozzle pipe varied within a wide interval of values. The results could indicate nonuniformity of the Cs-137 distribution in ocean bottom sediments as well as the penetration of significant amounts of Cs-137 to large depths. The main error resulted from the sampling technique employed because the upper part of the sediment could be lost. In 1982, a special ground-sampling device, with which the upper layer of sediments in the water layer close to the ocean bottom could be sampled, was tested in the Gulf of Finland and the Northeastern part of the Baltic Sea. The results of a layerwise determination of the Cs-137 concentration in samples of ocean bottom sediments of the Gulf of Finland and of the Baltic Sea are listed. The new soil-sampling device for picking samples of ocean sediments of undisturbed stratification will allow a correct determination of the radionuclide accumulation in the upper layers of ocean bottom sediments in the Baltic Sea

Mechanisms of Left Ventricular Dysfunction Assessed by Layer-Specific Strain Analysis in Patients With Repaired Tetralogy of Fallot.

Science.gov (United States)

Yamada, Mariko; Takahashi, Ken; Kobayashi, Maki; Yazaki, Kana; Takayasu, Hirobumi; Akimoto, Katsumi; Kishiro, Masahiko; Inage, Akio; Yoshikawa, Tadahiro; Park, In-Sam; Nakanishi, Keisuke; Kawasaki, Shiori; Shimizu, Toshiaki

2017-05-25

Left ventricular (LV) dysfunction in patients with repaired tetralogy of Fallot (rTOF) is an important risk factor for adverse outcomes. The aim of this study was to assess the details and time course of such LV dysfunction using layer-specific strain analysis by echocardiography.Methods and Results:The 66 patients with rTOF (mean age, 16.3±9.3 years) were divided into 3 groups (T1: 4-10 years, T2: 11-20 years, T3: 21-43 years), and 113 controls of similar age (mean age, 17.2±9.3 years) were divided into 3 corresponding groups (C1, C2, and C3). Layer-specific longitudinal strain (LS) and circumferential strain (CS) of 3 myocardial layers (endocardial, midmyocardial, and epicardial) were determined by echocardiography. Basal and papillary endocardial CS values were decreased in T1 compared with C1. With the exception of papillary epicardial CS, basal/papillary CS and LS of all 3 layers decreased in T2 compared with C2. Excepting papillary epicardial CS, all other values were decreased in T3 compared with C3. Potential myocardial damage was found in the endocardium at the basal and papillary levels of the LV in young patients with rTOF, extending from the endocardium to the epicardium and from the base to the apex. This is the possible time course of LV dysfunction in patients with rTOF.

The dependence of the content of Cs137 forms in sod-podzolic sabulous soil of different degree of humidification on the basic soil tillage

International Nuclear Information System (INIS)

Tsybulko, N.N.; Ermolenko, A.V.; Lazarevich, S.S.

2011-01-01

The dependence of the content of 137 Cs-forms in sod-podzolic sabulous soils of different degree of humidification on the basic soil tillage is presented. Structure (in %) of plant available 137Cs in automorphic and semi-hydromorphic soils is shown. The influence of soil tillage type on 137Cs content is analyzed per 2007-2008. Content (in %) of plant available 137Cs in automorphic and semi-hydromorphic soils during moldboard plowing, beardless plowing, surface disc plowing and minimum tillage is evaluated. In sod-podzolic sabulous soils with 137 Cs pollution density which equals to 13-15 Cu/km2 the content of the accessible for plants forms (water-soluble, exchangeable, mobile forms) makes in average 9-11%; of those inaccessible (not exchangeable, fixed) 89-91%. It is established, that the degree of the hydromorphic feature in sod-podzolic sabolous soil influence the content of accessible forms of 1376cs in its top layer. The chisel tillage and the minimum tillage make it possible to decrease the accessible 137Cs connections by 2-4%

Estimation of average burnup of damaged fuels loaded in Fukushima Dai-ichi reactors by using the 134Cs/137Cs ratio method

International Nuclear Information System (INIS)

Endo, T.; Sato, S.; Yamamoto, A.

2012-01-01

Average burnup of damaged fuels loaded in Fukushima Dai-ichi reactors is estimated, using the 134 Cs/ 137 Cs ratio method for measured radioactivities of 134 Cs and 137 Cs in contaminated soils within the range of 100 km from the Fukushima Dai-ichi nuclear power plants. As a result, the measured 134 Cs/ 137 Cs ratio from the contaminated soil is 0.996±0.07 as of March 11, 2011. Based on the 134 Cs/ 137 Cs ratio method, the estimated burnup of damaged fuels is approximately 17.2±1.5 [GWd/tHM]. It is noted that the numerical results of various calculation codes (SRAC2006/PIJ, SCALE6.0/TRITON, and MVP-BURN) are almost the same evaluation values of 134 Cs/ 137 Cs ratio with same evaluated nuclear data library (ENDF-B/VII.0). The void fraction effect in depletion calculation has a major impact on 134 Cs/ 137 Cs ratio compared with the differences between JENDL-4.0 and ENDF-B/VII.0. (authors)

Modeling dynamics of {sup 137}Cs in forest surface environments: Application to a contaminated forest site near Fukushima and assessment of potential impacts of soil organic matter interactions

Energy Technology Data Exchange (ETDEWEB)

Ota, Masakazu, E-mail: ohta.masakazu@jaea.go.jp; Nagai, Haruyasu; Koarashi, Jun

2016-05-01

A process-based model for {sup 137}Cs transfer in forest surface environments was developed to assess the dynamic behavior of Fukushima-derived {sup 137}Cs in a Japanese forest. The model simulation successfully reproduced the observed data from 3 year migration of {sup 137}Cs in the organic and mineral soil layers at a contaminated forest near Fukushima. The migration of {sup 137}Cs from the organic layer to the mineral soil was explained by the direct deposition pattern on the forest floor and the turnover of litter materials in the organic layer under certain ecological conditions. Long-term predictions indicated that more than 90% of the deposited {sup 137}Cs would remain within the top 5 cm of the soil for up to 30 years after the accident, suggesting that the forest acts as an effective long-term reservoir of {sup 137}Cs with limited transfer via the groundwater pathway. The model was also used to explore the potential impacts of soil organic matter (SOM) interactions on the mobility and bioavailability of {sup 137}Cs in the soil–plant system. The simulation results for hypothetical organic soils with modified parameters of {sup 137}Cs turnover revealed that the SOM-induced reduction of {sup 137}Cs adsorption elevates the fraction of dissolved {sup 137}Cs in the soil solution, thereby increasing the soil-to-plant transfer of {sup 137}Cs without substantially altering the fractional distribution of {sup 137}Cs in the soil. Slower fixation of {sup 137}Cs on the flayed edge site of clay minerals and enhanced mobilization of the clay-fixed {sup 137}Cs in organic-rich soils also appeared to elevate the soil-to-plant transfer of {sup 137}Cs by increasing the fraction of the soil-adsorbed (exchangeable) {sup 137}Cs. A substantial proportion (approximate 30%–60%) of {sup 137}Cs in these organic-rich soils was transferred to layers deeper than 5 cm decades later. These results suggested that SOM influences the behavior of {sup 137}Cs in forests over a prolonged

Long-term monitoring and analysis of 90Sr and 137Cs concentrations in rice, wheat and soils in Japan from 1959 to 2000

International Nuclear Information System (INIS)

Komamura, M.; Tsumura, A.; Yamaguchi, N.; Fujiwara, H.; Kihou, N.; Kodaira, K.

2006-01-01

Atmospheric nuclear tests in the 1950s and thereafter had showered radioactive fallout throughout Japan. Therefore, radioactive contamination of crops cultivated in Japan was concerned. We continued to monitor concentrations of 90Sr and 137Cs in rice, wheat and soils collected annually from sixteen national and prefectural experimental farms for forty-two years, from 1959 to 2000. In 1963, when the largest annual precipitation of radioactive fallout was observed, 90Sr and 137Cs concentration in rice and wheat reached at their maximum; 0.27 Bq/kg for 90Sr and 4.2 Bq/kg for 137Cs in polished rice and 12 Bq/kg for 90Sr and 44 Bq/kg for 137Cs in wheat grain. The concentration of 90Sr and 137Cs in the plowed layer of paddy and upland soils reached maximum from 1963 to 1966. After 1966, concentrations of 90Sr and 137Cs in polished rice, wheat grain, and soils were gradually decreased although there were some minor fluctuations. The Chernobyl nuclear power plant accident in 1986 caused contamination of wheat grain by 137Cs up to 6.0 Bq/kg. However, the concentration of 137Cs in wheat grain decreased to its normal level in the following year. There was no evidence for the polished rice contamination in Japan that could be ascribed to the accident at Chernobyl. Based on the analyses of the data above, we made several interesting findings as follows: a) The accumulated amounts of 90Sr and 137Cs in fallout during cultivation period were highly correlated with those concentrations in husked rice, polished rice and wheat grain. The estimate equations derived from the correlations were accurate enough for quick prediction of contamination level of polished rice and wheat grain based on 90Sr and 137Cs contents in fallout in case of contingencies. b) The sensitive response of 90Sr and 137Cs in polished rice and wheat grain to concentrations of fallout suggested that direct absorption of 90Sr and 137Cs from radioactive fallout deposited on plant body played important role. In 1963

Surface chemical analysis and ab initio investigations of CsI coated C fiber cathodes for high power microwave sources

Science.gov (United States)

Vlahos, Vasilios; Morgan, Dane; LaCour, Matthew; Golby, Ken; Shiffler, Don; Booske, John H.

2010-02-01

CsI coated C fiber cathodes are promising electron emitters utilized in field emission applications. Ab initio calculations, in conjunction with experimental investigations on CsI-spray coated C fiber cathodes, were performed in order to better understand the origin of the low turn-on E-field obtained, as compared to uncoated C fibers. One possible mechanism for lowering the turn-on E-field is surface dipole layers reducing the work function. Ab initio modeling revealed that surface monolayers of Cs, CsI, Cs2O, and CsO are all capable of producing low work function C fiber cathodes (1 eV<Φ<1.5 eV), yielding a reduction in the turn-on E-field by as much as ten times, when compared to the bare fiber. Although a CsI-containing aqueous solution is spray deposited on the C fiber surface, energy dispersive x-ray spectroscopy and scanning auger microscopy measurements show coabsorption of Cs and I into the fiber interior and Cs and O on the fiber surface, with no surface I. It is therefore proposed that a cesium oxide (CsxOy) surface coating is responsible, at least in part, for the low turn E-field and superior emission characteristics of this type of fiber cathode. This CsxOy layer could be formed during preconditioning heating. CsxOy surface layers cannot only lower the fiber work function by the formation of surface dipoles (if they are thin enough) but may also enhance surface emission through their ability to emit secondary electrons due to a process of grazing electron impact. These multiple electron emission processes may explain the reported 10-100 fold reduction in the turn-on E-field of coated C fibers.

137Cs in the western South Pacific Ocean

International Nuclear Information System (INIS)

Yamada, Masatoshi; Wang Zhongliang

2007-01-01

The 137 Cs activities were determined for seawater samples from the East Caroline, Coral Sea, New Hebrides, South Fiji and Tasman Sea (two stations) Basins of the western South Pacific Ocean by γ spectrometry using a low background Ge detector. The 137 Cs activities ranged from 1.4 to 2.3 Bq m -3 over the depth interval 0-250 m and decreased exponentially from the subsurface to 1000 m depth. The distribution profiles of 137 Cs activity at these six western South Pacific Ocean stations did not differ from each other significantly. There was a remarkable difference for the vertical profiles of 137 Cs activity between the East Caroline Basin station in this study and the GEOSECS (Geochemical Ocean Sections Study) station at the same latitude in the Equatorial Pacific Ocean; the 137 Cs inventory over the depth interval 100-1000 m increased from 400 ± 30 Bq m -2 to 560 ± 30 Bq m -2 during the period from 1973 to 1992. The total 137 Cs inventories in the western South Pacific Ocean ranged from 850 ± 70 Bq m -2 in the Coral Sea Basin to 1270 ± 90 Bq m -2 in the South Fiji Basin. Higher 137 Cs inventories were observed at middle latitude stations in the subtropical gyre than at low latitude stations. The 137 Cs inventories were 1.9-4.5 times (2.9 ± 0.7 on average) and 1.7-4.3 times (3.1 ± 0.7 on average) higher than that of the expected deposition density of atmospheric global fallout at the same latitude and that of the estimated 137 Cs deposition density in 10 o latitude by 10 deg. longitude grid data obtained by Aoyama et al. [Aoyama M, Hirose K, Igarashi Y. Re-construction and updating our understanding on the global weapons tests 137 Cs fallout. J Environ Monit 2006;8:431-438], respectively. The possible processes for higher 137 Cs inventories in the western South Pacific Ocean than that of the expected deposition density of atmospheric global fallout may be attributable to the inter-hemisphere dispersion of the atmospheric nuclear weapons testing 137 Cs from

Coherent Population Trapping Resonances in Cs Atomic Vapor Layers of Micrometric Thickness

Directory of Open Access Journals (Sweden)

A. Krasteva

2011-01-01

Full Text Available We report on a novel behavior of the electromagnetically induced absorption (EIA resonance observed on the D2 line of Cs for atoms confined in cells with micrometric thickness. With the enhancement of light intensity, the EIA resonance amplitude suffers from fast reduction, and even at very low intensity (W < 1 mW/cm2, resonance sign reversal takes place and electromagnetically induced transparency (EIT resonance is observed. Similar EIA resonance transformation to EIT one is not observed in conventional cm-size cells. A theoretical model is proposed to analyze the physical processes behind the EIA resonance sign reversal with light intensity. The model involves elastic interactions between Cs atoms as well as elastic interaction of atom micrometric-cell windows, both resulting in depolarization of excited state which can lead to the new observations. The effect of excited state depolarization is confirmed also by the fluorescence (absorption spectra measurement in micrometric cells with different thicknesses.

The interaction of CsCl with films of solid water

CERN Document Server

Borodin, A; Krischok, S; Kempter, V

2003-01-01

The interaction of CsCl molecules with films of solid water (three layers thick, typically), deposited on a tungsten crystal at 130 K, was studied. Metastable impact electron spectroscopy (MIES) and UPS(HeI) were applied to study the emission from Cl3p and Cs5p and the highest occupied states 1b sub 1 , 3a sub 1 and 1b sub 2 of molecular water. Below a critical stoichiometry of about CsCl centre dot nH sub 2 O with n=6 the UPS spectra are quite similar to those from chlorides solvated in liquid water in as much as the relative positions and intensities of the water and salt features are concerned; very little emission from the ionization of Cl3p and Cs5p is observed with MIES. We conclude that the CsCl molecules become solvated in the water film. As long as n>6, the water spectrum remains characteristic for condensed water; at n6, water molecules not involved directly into the hydration of the salt molecules desorb around 140 K. Around 160 K all water has disappeared from the surface. Above this temperature o...

Syntheses and crystal structures of BaAgTbS{sub 3}, BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and CsAgUTe{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Prakash, Jai; Beard, Jessica C.; Ibers, James A. [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States); Mesbah, Adel [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States); ICSM-UMR 5257 CNRS/CEA/UM2/ENSCM, Bat 426, BP 17171, 30207 Bagnols/Ceze (France)

2015-06-15

Five new quaternary chalcogenides of the 1113 family, namely BaAgTbS{sub 3}, BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and CsAgUTe{sub 3}, were synthesized by the reactions of the elements at 1173-1273 K. For CsAgUTe{sub 3} CsCl flux was used. Their crystal structures were determined by single-crystal X-ray diffraction studies. The sulfide BaAgTbS{sub 3} crystallizes in the BaAgErS{sub 3} structure type in the monoclinic space group C{sup 3},{sub 2h}-C2/m, whereas the tellurides BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and CsAgUTe{sub 3} crystallize in the KCuZrS{sub 3} structure type in the orthorhombic space group D{sup 1},{sub 2}{sup 7},{sub h}-Cmcm. The BaAgTbS{sub 3} structure consists of edge-sharing [TbS{sub 6}{sup 9-}] octahedra and [AgS{sub 5}{sup 9-}] trigonal pyramids. The connectivity of these polyhedra creates channels that are occupied by Ba atoms. The telluride structure features {sup 2}{sub ∞}[MLnTe{sub 3}{sup 2-}] layers for BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and {sup 2}{sub ∞}[AgUTe{sub 3}{sup 1-}] layers for CsAgUTe{sub 3}. These layers comprise [MTe{sub 4}] tetrahedra and [LnTe{sub 6}] or [UTe{sub 6}] octahedra. Ba or Cs atoms separate these layers. As there are no short Q..Q (Q = S or Te) interactions these compounds achieve charge balance as Ba{sup 2+}M{sup +}Ln{sup 3+}(Q{sup 2-}){sub 3} (Q = S and Te) and Cs{sup +}Ag{sup +}U{sup 4+}(Te{sup 2-}){sub 3}. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Assessment of the transfer of 137Cs in three types of vegetables consumed in Hong Kong

International Nuclear Information System (INIS)

Yu, K.N.; Mao, S.Y.; Young, E.C.M.

1998-01-01

A dynamic food chain model has been built for the modeling of the transfer of 137 Cs in three types of vegetables consumed in Hong Kong, namely, white flowering cabbage (Brassica chinensis), head lettuce (Lactuca sativa) and celery (Apium graveolens). Some parameters have been estimated from the experimental data obtained in this work. The experimental data include the transfer factors of 137 Cs from soil to the different vegetable species which are determined through high resolution gamma spectrometry, maximum crop biomasses for the vegetable species, the dry-to-fresh ratios for the vegetable species, the bulk density of soil layers and the average concentration of 137 Cs in air. The derived parameters include the deposition rate and the root uptake rate, information for tillage, the logistic growth model and radionuclide concentrations in vegetables. The dynamic food chain model is solved by the Birchall-James algorithm to give the 137 Cs concentration in subsurface soil, from the 0.1-25 cm soil layer, and the 137 Cs concentration in harvested and unwashed vegetables. As validation of the model and parameters, the concentrations obtained experimentally and from the model are compared and are found to be in good agreement

Efficiency enhancement of InGaN/GaN multiple quantum wells with graphene layer

International Nuclear Information System (INIS)

Deng, Zhen; Li, Zishen; Jiang, Yang; Ma, Ziguang; Fang, Yutao; Li, Yangfeng; Wang, Wenxin; Jia, Haiqiang; Chen, Hong

2015-01-01

In this work, a novel hybrid graphene/InGaN-based multiple quantum wells (MQWs) structure has been fabricated. Compared to the sample conventional structure (CS), the utilization of graphene transferred on top GaN layer significantly enhances the internal quantum efficiency and relatively photoluminescence intensity. Furthermore, the excitons in the MQWs of sample hybrid structure (HS) have a shorter decay lifetime of 3.4 ns than that of 6.7 ns for sample CS. These results are probably attributed to the free carriers in the graphene layer, which can screen the piezoelectric field in the active region and thus present a free quantum-confined Stark effect-like behavior. Our work demonstrates that the graphene on the top GaN layer can effectively increase the recombination rate in sample HS, which may further improve LEDs' performance. (orig.)

Molecular composition of light portion from CS{sub 2}/NMP-extractable fraction of Hami and Lingwu coals

Energy Technology Data Exchange (ETDEWEB)

Ji-Xian Jia; Zhi-Min Zong; Xin Jin; Chan-Min Liu; Hong Zhang; Yan Li; Bin Huang; Xian-Yong Wei [China University of Mining and Technology, Xuzhou (China). School of Chemical Engineering

2007-07-01

Hami and Lingwu coals were extracted with a CS{sub 2}/NMP mixed solvent (1:1 by vol) under ultrasonic irradiation at room temperature. After removing most of CS{sub 2} and NMP by distillation under ambient and reduced pressures, respectively, from the extraction solution, the extract was extracted with petroleum ether (PE) in a Soxhlet extractor. Two layers appeared after concentrating the PE-extractable solution. GC/MS analysis shows that the upper layer mainly consists of normal and branched alkanes along with cyclanes, whereas main components in the lower layer are non-substituted and substituted arenes along with heteroatom-containing organic compounds. 15 refs., 2 figs., 1 tab.

Radiocesium storage in soil microbial biomass of undisturbed alpine meadow soils and its relation to 137Cs soil-plant transfer

International Nuclear Information System (INIS)

Stemmer, Michael; Hromatka, Angelika; Lettner, Herbert; Strebl, Friederike

2005-01-01

This study focuses on radiocesium storage in soil microbial biomass of undisturbed alpine meadow sites and its relation to the soil-to-plant transfer. Soil and plant samples were taken in August 1999 from an altitude transect (800-1600 m.a.s.l.) at Gastein valley, Austria. Soil samples were subdivided into 3-cm layers for analyses of total, K 2 SO 4 -extractable and microbially stored 137 Cs. Microbial biomass was measured by the fumigation extraction method, and fungal biomass was quantified using ergosterol as biomarker molecule. In general, the quantity of 137 Cs stored in the living soil microbial biomass was relatively small. At the high-altitude meadows, showing high amounts of fungal biomass, microbially stored 137 Cs amounted to 0.64 ± 0.14 kBq m -2 which corresponds to about 1.2-2.7% of the total 137 Cs soil inventory. At lower altitudes, microbial 137 Cs content was distinctly smaller and in most cases not measurable at all using the fumigation extraction method. However, a positive correlation between the observed soil-to-plant aggregated transfer factor, microbially stored 137 Cs and fungal biomass was found, which indicates a possible role of fungal biomass in the storage and turnover of 137 Cs in soils and in the 137 Cs uptake by plants

Selectivity of crystalline Cesup(IV) phosphate sulphate hydrates for Li+, Na+, K+, Rb+ Cs+, and NH4+ in absolute methanol and absolute dimethylsulphoxide

International Nuclear Information System (INIS)

Koenig, K.H.; Psotta, L.

1978-01-01