Relevant bibliographies by topics / Small-angle X-ray and neutron scattering

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Small-angle X-ray and neutron scattering'

Author: Grafiati
Published: 4 February 2023

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Journal articles on the topic "Small-angle X-ray and neutron scattering"

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Seto, Hideki, and Michihiro Nagao. "Small Angle X-ray and Neutron Scattering." hamon 13, no. 1 (2003): 29–32. http://dx.doi.org/10.5611/hamon.13.29.

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Hoell, Armin, Dragomir Tatchev, Sylvio Haas, Jörg Haug, and Peter Boesecke. "On the determination of partial structure functions in small-angle scattering exemplified by Al89Ni6La5alloy." Journal of Applied Crystallography 42, no. 2 (January 24, 2009): 323–25. http://dx.doi.org/10.1107/s0021889808042453.

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A comparison between the resonant scattering curve obtained by anomalous small-angle X-ray scattering at the X-ray absorption edge of Ni and the complementary small-angle neutron scattering curve from an Al89Ni6La5alloy sample is reported. The sample does not comply with the two-phase approximation. The two resulting scattering curves are approximately proportional to each other in this particular case. The anomalous small-angle X-ray scattering resonant curve at the Ni absorption edge equals the Ni–Ni partial structure factor and, owing to the favourable neutron scattering lengths of Ni, La and Al, the neutron scattering curve is also proportional to that partial structure factor.
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Gommes, Cedric J., Sebastian Jaksch, and Henrich Frielinghaus. "Small-angle scattering for beginners." Journal of Applied Crystallography 54, no. 6 (November 25, 2021): 1832–43. http://dx.doi.org/10.1107/s1600576721010293.

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Many experimental methods are available for the characterization of nanostructures, but most of them are limited by stringent experimental conditions. When it comes to analysing nanostructures in the bulk or in their natural environment – even as ordinary as water at room temperature – small-angle scattering (SAS) of X-rays or neutrons is often the only option. The rapid worldwide development of synchrotron and neutron facilities over recent decades has opened unprecedented possibilities for using SAS in situ and in a time-resolved way. But, in spite of its huge potential in the field of nanomaterials in general, SAS is covered far less than other characterization methods in non-specialized curricula. Presented here is a rigorous discussion of small-angle scattering, at a technical level comparable to the classical undergraduate coverage of X-ray diffraction by crystals and which contains diffraction as a particular case.
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MATSUOKA, Hideki. "Introduction to Small-angle X-ray and Neutron Scattering." Journal of Japan Oil Chemists' Society 49, no. 10 (2000): 1163–71. http://dx.doi.org/10.5650/jos1996.49.1163.

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Henderson, Stephen J. "Isotope effects in solution small-angle X-ray scattering." Journal of Applied Crystallography 32, no. 1 (February 1, 1999): 113–14. http://dx.doi.org/10.1107/s0021889898010498.

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While the difference between using heavy and light water as solvents for small-angle neutron scattering experiments is well known, the lesser difference for the case of small-angle X-ray scattering with these same isotopes of water has, as yet, not been reported. This difference for the case of X-rays is discussed and quantified for several familiar materials: polystyrene latexes, proteins and lipids.
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Suzuya, Kentaro, Michihiro Furusaka, Noboru Watanabe, Makoto Osawa, Kiyohito Okamura, Kaoru Shibata, Tomoaki Kamiyama, and Kenji Suzuki. "Mesoscopic structure of SiC fibers by neutron and x-ray scattering." Journal of Materials Research 11, no. 5 (May 1996): 1169–78. http://dx.doi.org/10.1557/jmr.1996.0151.

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Mesoscopic structures of SiC fibers produced from polycarbosilane by different methods were studied by diffraction and small-angle scattering of neutrons and x-rays. Microvoids of a size of 4–10 Å in diameter have been observed for the first time by neutron scattering in a medium momentum transfer range (Q = 0.1–1.0 Å−1). The size and the volume fraction of β–SiC particles were determined for fibers prepared at different heat-treatment temperatures. The results show that wide-angle neutron scattering measurements are especially useful for the study of the mesoscopic structure of multicomponent materials.
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Sastry, P. U., V. K. Aswal, and A. G. Wagh. "Small angle neutron scattering and small angle X-ray scattering studies of platinum-loaded carbon foams." Pramana 71, no. 5 (November 2008): 1075–78. http://dx.doi.org/10.1007/s12043-008-0226-6.

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Härk, Eneli, and Matthias Ballauff. "Carbonaceous Materials Investigated by Small-Angle X-ray and Neutron Scattering." C 6, no. 4 (December 19, 2020): 82. http://dx.doi.org/10.3390/c6040082.

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Carbonaceous nanomaterials have become important materials with widespread applications in battery systems and supercapacitors. The application of these materials requires precise knowledge of their nanostructure. In particular, the porosity of the materials together with the shape of the pores and the total internal surface must be known accurately. Small-angle X-ray scattering (SAXS) and small-angle neutron scattering (SANS) present the methods of choice for this purpose. Here we review our recent investigations using SAXS and SANS. We first describe the theoretical basis of the analysis of carbonaceous material by small-angle scattering. The evaluation of the small-angle data relies on the powerful concept of the chord length distribution (CLD) which we explain in detail. As an example of such an evaluation, we use recent analysis by SAXS of carbide-derived carbons. Moreover, we present our SAXS analysis on commercially produced activated carbons (ACN, RP-20) and provide a comparison with small-angle neutron scattering data. This comparison demonstrates the wealth of additional information that would not be obtained by the application of either method alone. SANS allows us to change the contrast, and we summarize the main results using different contrast matching agents. The pores of the carbon nanomaterials can be filled gradually by deuterated p-xylene, which leads to a precise analysis of the pore size distribution. The X-ray scattering length density of carbon can be matched by the scattering length density of sulfur, which allows us to see the gradual filling of the nanopores by sulfur in a melt-impregnation procedure. This process is important for the application of carbonaceous materials as cathodes in lithium/sulfur batteries. All studies summarized in this review underscore the great power and precision with which carbon nanomaterials can be analyzed by SAXS and SANS.
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Russell, T. P., J. S. Lin, S. Spooner, and G. D. Wignall. "Intercalibration of small-angle X-ray and neutron scattering data." Journal of Applied Crystallography 21, no. 6 (December 1, 1988): 629–38. http://dx.doi.org/10.1107/s0021889888004820.

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Schmidt, P. W. "Collimation effects in small-angle X-ray and neutron scattering." Journal of Applied Crystallography 21, no. 6 (December 1, 1988): 602–12. http://dx.doi.org/10.1107/s0021889888006375.

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Dissertations / Theses on the topic "Small-angle X-ray and neutron scattering"

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Van, Delinder Kurt William. "The investigation of the molecular mechanism of rhodopsin activation by small angle neutron scattering and small angle x-ray scattering techniques." Thesis, Wayne State University, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=1604674.

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Rhodopsin is a visual pigment found within the rod photoreceptor cells of the retina. It is a visual protein found within human beings and commonly shared amongst other vertebrate species. The major pigment protein is responsible for converting photons into chemical signals, which stimulates biological processes in the nervous system, and this allows the ability to then sense light.

The process of how rhodopsin is activated is believed to be understood with the introduction of a time ordered sequence of intermediate states. However, there are still major gaps and inconsistencies regarding the large-scale conformational changes that follow photoactivation.

The purpose of our experimental research is to use small angle neutron and x-ray scattering techniques to illuminate the structural changes and dynamics of rhodopsin that lead to the activation of the photoreceptor, and thus triggering of the amplified visual response.

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Rai, Durgesh K. "Quantification of Fractal Systems using Small Angle Scattering." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1377870724.

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Ku, Chwen-Yuan. "Small-angle X-ray and neutron scattering studies of 3-component microemulsion and micellar solution of semifluorinated copolymers." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/38846.

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Kulkarni, Amit S. "Nature of Branching in Disordered Materials." University of Cincinnati / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1190655419.

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Ivanov, Ivan Yavorov. "Etude biophysique et structurale du complexe de réplication des virus à ARN négatif." Thesis, Grenoble, 2011. http://www.theses.fr/2011GRENV083/document.

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Les rhabdovirus, dont les virus de la stomatite vésiculaire (VSV) et de la rage (RAV) constituent des prototypes, sont des virus enveloppés dont le génome est constitué d'une seule molécule d'ARN simple brin de polarité négative qui font partie de l'ordre des Mononegavirales (MNV). La machinerie de transcription/réplication de ces virus est constituée de l'ARN génomique et de trois protéines qui sont communes à tous les virus de l'ordre des MNV, la (N) qui encapside le génome viral, la grande sous-unité de l'ARN polymérase ARN dépendante (L) et la phosphoprotéine (P) qui est un cofacteur non-catalytique de la L et sert de chaperonne à la N. Le premier objectif de mon travail de thèse consistait à déterminer la structure cristallographique du domaine de dimérisation de la phosphoprotéine du virus de la rage. La P des rhabdovirus est une protéine modulaire qui contient deux régions intrinsèquement désordonnée, un domaine central responsable la dimérisation et un domaine C-terminal responsable de la fixation sur la matrice N-ARN. Le modèle atomique obtenu à une résolution de 1.5A montre que la structure est très différente de celle du domaine correspondant chez VSV. Le second objectif de mon travail était la caractérisation structurale de la grande sous-unité L de la polymérase du virus de la stomatite vésiculaire. Cette enzyme de 2109,aa, possède six régions conservées. Le domaine conservé III comprend les régions impliquées dans l'activité de polymérisation et les domaines V et VI sont responsables de la formation de la coiffe des ARNm. Plusieurs stratégies ont été envisagées successivement. (1) Sur la base de prédictions de structures secondaires et de prédictions de désordre, nous avons essayé d'exprimer différents fragments en système d'expression bactérien. Les constructions testées se sont avérées insolubles et certaines d'entre elles fixaient GroEL, indiquant un problème de repliement. (2) Nous avons alors essayé d'exprimer la L seule ou en complexe avec la P en système d'expression eucaryote. La purification s'est avérée impossible, la protéine L restant toujours associées à des protéines cellulaires visibles par coloration au bleu de Coommassie. (3) Finalement nous avons réussi à purifier la polymérase à partir de virus entier. La préparation de la polymérase était très homogène et a permis d'entreprendre une caractérisation par microscopie électronique. Une classification d'images a permis de construire un premier modèle à basse résolution. Le modèle révèle la présence d'un domaine annulaire avec plusieurs domaines structurés attachés au coeur de la polymérase. La cryo-microscopie électronique et la tomographie permettront d'obtenir plus de détails sur cette protéine
Rhabdoviruses, including vesicular stomatitis virus (VSV) and rabies virus (RAV), are enveloped viruses which genome is made of a single molecule of negative-sense RNA and are classified in the order Mononegavirales (MNV). The transcription/replication machinery of these viruses consists of the genomic RNA and of three proteins, which are common to all other viruses of the order MNV, a nucleoprotein (N) that encapsidates the viral genome, a large subunit of the RNA-dependent RNA polymerase (L) and a phosphoprotein (P) that acts as a non-catalytic cofactor of L and a chaperone of N. The first goal of my research project was to determine the crystallographic structure of the dimerization domain of the rabies virus phosphoprotein. The P protein of the rhabdoviruses is a modular protein, which contains two intrinsically disordered regions, a central dimerization domain and a C-terminal domain involved in binding to the N-RNA template. The atomic model obtained at a resolution of 1.5 A showed that the structure is different from that of the corresponding domain of VSV. The second goal was the structural characterization of the large subunit L of VSV polymerase. The enzyme of 2109 aa has six conserved regions. Conserved region III includes the residues involved in the RNA synthesis activity, whereas domains V and VI are involved in mRNA capping formation. Three strategies were successively developed: (1) On the basis of secondary structure and disorder predictions, we tried to express different fragments in bacterial expression systems. These constructions appeared to be insoluble and some of them bound GroEL suggesting a folding problem; (2) We tried to express L alone or co-express it with P in eukaryotic expression system. The purification appeared to be impossible, the L protein always remaining associated with host-cell proteins in amounts detectable by Coommassie staining; (3) We succeeded in purifying the L protein from the virus. The L samples were homogenous and allowed a characterization by electron microscopy. Image classes allowed the reconstruction of a first low-resolution model. This model revealed the presence of a large ring-like domain and several globular domains. Cryo-electron microscopy and tomography should lead to a more detailed description of this protein
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Kinder, S. H. "Small angle neutron scattering and #gamma#-ray scattering for the study of second phase precipitation in semiconductor silicon and the Nimonic superalloy PE16." Thesis, University of Reading, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.378199.

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Liu, Yun 1973. "Studies of structure and dynamics of biological macro-molecular assemblies by low angle neutron diffraction and inelastic X-ray scattering." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/34438.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Nuclear Engineering, 2005.
Includes bibliographical references (leaves 141-148).
This thesis is organized into two parts which focus on the studies of the dynamic structure factor and static inter-particle structure factor respectively. In the first part, we have measured and analyzed the dynamic structure factors of aligned 40 wt% calfthymus Na-DNA molecules with the inelastic X-ray scattering (IXS). In the second part, we have developed a new efficient method to calculate the inter-particle structure factor in a simple fluid interacting with a two-Yukawa term potential and apply it to study the kinetic phase diagram and analyze the small angle neutron scattering (SANS) intensity distribution of colloidal systems. By analyzing the dynamic structure factor measured with IXS, the phonon dispersion relations of 40 wt% calf-thymus Na-DNA with different counterion atmosphere are constructed. It is found that the addition of extra counterions will increase phonon damping at small scattering wave vector, Q. At the intermediate Q range (12.5 nm- < Q < 22.5 nm-l), it may even overdamp the phonon so that the phonon feature can not be extracted from the IXS spectra. The measured sound speed is 3100m/s, which is much higher than the sound speed, - 1800m/s, obtained by Brillouin light scattering. This difference shows that the atoms of DNA molecules are closely coupled to the surrounding water molecules.
(cont.) Therefore, the different dynamic response of water molecules in different Q range affects the overall dynamic response of the hydrated DNA molecules. By analyzing the IXS spectra, the intermediate scattering function is extracted and shows a clear two step relaxation with the fast relaxation time ranging from 0.1 to 4 ps and the slow relaxation time ranging from 2 to 800 ps. In order to understand the phase behavior and the interactive potential of a colloidal system, we have developed a new and efficient method to calculate the inter-particle structure factor of a simple fluid interacting with a two-Yukawa term potential. We have applied this method to study the kinetic phase diagram of a system interacting with a short-range attraction and a long-range repulsion. A new glass phase, cluster glass, is determined through the theoretical analysis by the mode coupling theory (MCT). The SANS intensity distribution of cytochrome C protein molecules in solutions is measured and analyzed with our method. A sharp rising intensity at very low Q value has been consistently observed, which is named zero-Q peak. The existence of the zero-Q peak implies that a weak long-range attraction between protein molecules in solutions exists and has a even longer range than the electrostatic repulsion.
by Yun Liu.
Ph.D.
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Ouali, Chakib. "Caractérisation multi-échelle de l’écoulement de mousses en milieux poreux en contexte EOR." Thesis, Sorbonne université, 2019. http://www.theses.fr/2019SORUS001/document.

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L’utilisation de la mousse en récupération assistée du pétrole (Enhanced Oil Recovery, EOR) présente un avantage indéniable par rapport à l’injection du gaz seul pour pallier les problèmes de ségrégation gravitaire et de digitations visqueuses. Son utilisation systématique en ingénierie du réservoir nécessite des connaissances plus approfondies sur son comportement en milieu poreux. La littérature montre deux types d’approches expérimentales basées soit sur des études pétrophysiques effectuées sur des systèmes poreux 3D et basées sur des mesures de pressions intégrées sur l’ensemble du milieu poreux, soit sur des études micro-fluidiques qui permettent une visualisation directe de l’écoulement mais qui sont limitées à des systèmes modèles dans des géométries à 1 ou 2 dimensions. L’objectif de cette thèse est de faire le pont entre ces deux approches. La stratégie proposée consiste à caractériser in situ l’écoulement de la mousse dans des milieux poreux 3D à différentes échelles, en utilisant des techniques complémentaires permettant d’accéder à une large gamme de résolutions spatiale et temporelle. Un environnement instrumenté donnant accès aux mesures pétro-physiques classiques a été développé puis couplé à différentes cellules d’observation conçues spécifiquement pour chaque instrument de caractérisation. Dans un premier temps, un scanner X a été utilisé pour décrire et visualiser les écoulements de la mousse à l’échelle de la carotte. La rhéologie de la mousse à cette échelle a pu être étudiée en fonction des conditions d’injections comme la vitesse interstitielle du gaz et la qualité de mousse. Dans un deuxième temps, la technique de diffusion des neutrons aux petits angles (SANS) a permis de sonder la texture de la mousse en écoulement sur trois ordres de grandeurs en taille. Des informations in situ sur la texture de la mousse en écoulement (taille et densité des bulles et des lamelles) ont pu être mesurées pour différentes qualités de mousse puis en fonction de la distance au point d’injection. Une comparaison avec les caractéristiques géométriques du milieu poreux a également été effectuée. Dans un troisième temps, la micro-tomographie X rapide haute résolution sur Synchrotron a été utilisée pour visualiser la mousse en écoulement à l’échelle du pore. Cette technique a permis de confirmer de visu certaines caractéristiques de la mousse mesurées par SANS et de décrire en sus les effets d’intermittence du piégeage de la mousse. Cette étude constitue une étape importante de la caractérisation multi-échelle de l’écoulement des mousses en milieux poreux 3D et apporte des éléments de réponse à certaines hypothèses admises
Foam has long been used as a mobility control agent in Enhanced Oil Recovery (EOR) processes to enhance sweep efficiency and overcome gravity segregation, viscous fingering and gas channeling, which are gas-related problems when the latter is injected alone in the reservoir. However, the systematic use of foam in reservoir engineering requires more in-depth knowledge of its dynamics in porous media. The literature shows two types of experimental approaches based either on petrophysical studies carried out on 3D porous systems and based on pressure measurements, or on microfluidic studies that allow direct visualization of foam flow but are limited to 1D or 2D model systems. The research investigated in this thesis aims to bridge the gap between these two approaches. The proposed strategy is to characterize in situ the foam flow in 3D porous media with techniques providing a wide range of temporal and spatial resolutions. A coreflood setup giving access to classical petro-physical measurements was developed and then coupled to different observation cells designed specifically for each characterization instrument. First, an X-ray CT scanner was used to describe and visualize the foam flow at the core scale. The rheological behavior of foam on this scale was studied as a function of the injection conditions such as gas velocity and foam quality. Secondly, Small Angle Neutron Scattering (SANS) was used to probe the foam structure in situ during the flow, on a wide length scale, up to three orders of magnitude in size. In situ foam texture (size and density of bubbles and lamellae) was measured for different foam qualities and at different propagation distances from the injection point. A comparison to the geometric characteristics of the porous medium was also realized. Thirdly, High Resolution Fast X-ray Micro-tomography on a Synchrotron was used to visualize the foam flow at the pore scale. This allowed to confirm visually some foam characteristics measured with SANS and to investigate on local intermittent gas trapping and mobilization. This study is an important step in the multi-scale characterization of foam flow in 3D porous media and provides some answers to certain generally accepted assumptions
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Konko, Iuliia. "Aqueous solutions of complexes formed by model polyelectrolytes of opposite charges." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAE049/document.

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Cette thèse présente une étude des solutions aqueuses de trois complexes de polyélectrolytes (PECs) modèles. Les PECs résultent de la complexation de deux polyélectrolytes linéaires de charge opposée: un polycation (le PDADMA) et trois polyanions de longueur de persistance non électrostatique distinctes: le polystyrene sulfoné (PSS), le poly(α-méthyl styrène sulfoné) (PαMSS) et l’acide hyaluronique (HA). En plus de l’influence de la rigidité intrinsèque des polyanions sur la formation et la structure des PECs, les effets de la force ionique et de la méthode de préparation des solutions aqueuses de PECs ainsi que l’influence de la concentration des solutions binaires de polyélectrolytes initiales ont également été abordés. Nous suggérons que le processus de complexation entre polycations et polyanions en régimes semidilué et concentré est analogue à une gélification. Il y a toutefois une différence entre les deux complexes qui est reliée à la différence de rigidité intrinsèque
This PhD thesis presents a study of the aqueous solutions of three model polyelectrolyte complexes (PECs). PECs were formed between hydrophilic and highly charged linear macrocations of poly(diallyldimethyl ammonium) (PDADMA) and linear macroanions of distinct intrinsic persistence lengths: sulfonated polystyrene (PSS), sulfonated poly(α-methyl styrene) (PαMSS) and hyaluronate (HA). In addition to the effect of the macroion stiffness on the PEC formation and structure, those of the ionic strength and the way of preparing the PEC aqueous solutions as well as that of the concentration regimes of the initial PE aqueous solutions were also tackled. We suggest the complexation between macrocations and macroanions in the semidilute and concentrated regimes can be described as a universal gelation process. A difference between PDADMA-PSS and PDADMA-HA complexes is related to the primary self-assembling process and is associated with the distinct structural models for PECs
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Jalal, Noureddine. "Etude des agregats formes par neutralisation des chaines monocarboxylees par : diffusion aux petits angles des neutrons et des rayons x." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13137.

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Etude de polymeres possedant un seule fonction acide terminale neutralisee par des cations metalliques. Influence du cation, de la masse du precurseur et de la concentration sur l'association de chaines et de l'existence d'une concentration d'agregation critique
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Books on the topic "Small-angle X-ray and neutron scattering"

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A, Feĭgin L., and Taylor George W, eds. Structure analysis by small-angle x-ray and neutron scattering. New York: Plenum Press, 1987.

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Feigin, L. A., and D. I. Svergun. Structure Analysis by Small-Angle X-Ray and Neutron Scattering. Edited by George W. Taylor. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4757-6624-0.

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Paul, Amitesh. Low-Angle Polarized Neutron and X-Ray Scattering from Magnetic Nanolayers and Nanostructures. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-63224-7.

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Pająk, Lucjan. Nanoniejednorodoności materiałów a efekt małokątowego rozpraszania promieni rentgenowskich i neutronów. Katowice: Wydawn. Uniwersytetu Śląskiego, 2010.

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Svergun, D. I. Rentgenovskoe i neĭtronnoe malouglovoe rassei͡a︡nie. Moskva: "Nauka," Glav. red. fiziko-matematicheskoĭ lit-ry, 1986.

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1926-, Brumberger H., ed. Modern aspects of small-angle scattering. Dordrecht: Kluwer Academic Publishers, 1995.

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Carlo, Steven Roy. Small angle x-ray scattering and modelling studies of nitrogenase. Leicester: De MontfortUniversity, 1996.

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Anitas, Eugen Mircea. Small-Angle Scattering (Neutrons, X-Rays, Light) from Complex Systems. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-26612-7.

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Furugren, Bo. Biomolekyler studerade med la gvinkelro ntgenspridning =: Biomolecules studied by small-angle X-ray scattering. Uppsala: Sveriges lantbruksuniversitet, 1987.

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Kikō), Foton Fakutorī Kenkyūkai (2004 Kō-enerugī Kasokuki Kenkyū. Kō X-sen o mochiita dainamikku kōzō no kanōsei: Foton Fakutorī Kenkyūkai. Tsukuba-shi: High Energy Accelerator Research Organization, 2005.

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Book chapters on the topic "Small-angle X-ray and neutron scattering"

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Melnichenko, Yuri B. "Neutron and X-Ray Porosimetry." In Small-Angle Scattering from Confined and Interfacial Fluids, 173–204. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-01104-2_8.

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Wignall, George D. "Small Angle Neutron and X-Ray Scattering." In Physical Properties of Polymers Handbook, 407–20. New York, NY: Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-69002-5_23.

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Takeno, Hiroyuki. "Synchrotron Small-Angle X-Ray Scattering and Small-Angle Neutron Scattering Studies of Nanomaterials." In X-ray and Neutron Techniques for Nanomaterials Characterization, 717–60. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48606-1_13.

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Feigin, L. A., D. I. Svergun, and George W. Taylor. "X-Ray and Neutron Instrumentation." In Structure Analysis by Small-Angle X-Ray and Neutron Scattering, 249–74. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4757-6624-0_8.

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Laggner, P. "X-Ray and Neutron Small-Angle Scattering on Plasma Lipoproteins." In Modern Aspects of Small-Angle Scattering, 371–86. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8457-9_15.

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Vainio, Ulla. "Anomalous Small-Angle X-ray Scattering." In Neutrons and Synchrotron Radiation in Engineering Materials Science, 217–25. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527684489.ch13.

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Wignall, George D. "Combined Small-Angle Neutron and X-Ray Scattering Studies of Polymers." In Advances in X-Ray Analysis, 355–72. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2972-9_41.

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Williams, Claudine E., Roland P. May, and André Guinier. "Small-Angle Scattering of X-Rays and Neutrons." In X-ray Characterization of Materials, 211–54. Weinheim, Germany: Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527613748.ch4.

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Feigin, L. A., D. I. Svergun, and George W. Taylor. "General Principles of Small-Angle Diffraction." In Structure Analysis by Small-Angle X-Ray and Neutron Scattering, 25–55. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4757-6624-0_2.

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Petoukhov, M. V., and D. I. Svergun. "Small Angle X-Ray Scattering/Small Angle Neutron Scattering as Methods Complementary to NMR." In NMR of Biomolecules, 562–74. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527644506.ch35.

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Conference papers on the topic "Small-angle X-ray and neutron scattering"

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Mazumder, S., Abarrul Ikram, Agus Purwanto, Sutiarso, Anne Zulfia, Sunit Hendrana, and Zeily Nurachman. "Dynamical Scaling, Fractal Morphology and Small-angle Scattering." In NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906085.

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Knott, R. B., Abarrul Ikram, Agus Purwanto, Sutiarso, Anne Zulfia, Sunit Hendrana, and Zeily Nurachman. "Membrane Structure Studies by Means of Small-Angle Neutron Scattering (SANS)." In NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906088.

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Sari, Widya, Dian Fitriyani, Edy Giri Rachman Putra, Abdul Aziz bin Mohamed, Noorddin Ibrahim, and Abdul Aziz Bin Mohamed. "Fractal Structures on Silica Aerogels Containing Titanium: A Small Angle Neutron Scattering Study." In NEUTRON AND X-RAY SCATTERING IN ADVANCING MATERIALS RESEARCH: Proceedings of the International Conference on Neutron and X-Ray Scattering—2009. AIP, 2010. http://dx.doi.org/10.1063/1.3295595.

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Zeng, X. B., F. Liu, F. Xie, G. Ungar, C. Tschierske, J. E. Macdonald, Abarrul Ikram, et al. "Small Angle X-ray and Neutron Scattering in the Study of Polymers and Supramolecular Systems." In NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906097.

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Putra, E. Giri Rachman, and Abdul Aziz Bin Mohamed. "Small-Angle Neutron Scattering (SANS) Facility at BATAN for Nanostructure Studies in Materials Science and Biology." In NEUTRON AND X-RAY SCATTERING IN ADVANCING MATERIALS RESEARCH: Proceedings of the International Conference on Neutron and X-Ray Scattering—2009. AIP, 2010. http://dx.doi.org/10.1063/1.3295588.

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Mohamed, Abdul Aziz, Megat Harun Al Rashid Megat Ahmad, Faridah Md Idris, Azraf Azman, Rafhayudi Jamro, Mohd Rizal Mamat Ibrahim, Anwar Abdul Rahman, and Abdul Aziz Bin Mohamed. "Micro-focused Small Angle Neutron Scattering and Imaging for Science and Engineering Using RTP—A Preliminary Study." In NEUTRON AND X-RAY SCATTERING IN ADVANCING MATERIALS RESEARCH: Proceedings of the International Conference on Neutron and X-Ray Scattering—2009. AIP, 2010. http://dx.doi.org/10.1063/1.3295602.

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Ani, S. A., S. Pratapa, S. Purwaningsih, Triwikantoro, Darminto, E. Giri Rachman Putra, A. Ikram, et al. "Size and Correlation Analysis of Fe[sub 3]O[sub 4] Nanoparticles in Magnetic Fluids by Small-Angle Neutron Scattering." In NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906059.

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Ray, Debes, V. K. Aswal, Alka B. Garg, R. Mittal, and R. Mukhopadhyay. "Combined Small-angle Neutron and X-ray Scattering Studies of Block Copolymer-mediated Gold Nanoparticles." In SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3605906.

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Aliev, F. K., G. R. Alimov, A. Ikramov, A. K. Inoyatov, Muradin A. Kumakhov, A. T. Muminov, Tolib M. Muminov, et al. "Hard γ-quanta scattering on a smooth surface at very small slide angles." In International Conference on X-ray and Neutron Capillary Optics, edited by Muradin A. Kumakhov. SPIE, 2002. http://dx.doi.org/10.1117/12.489753.

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Hae-Jeong Lee, E. K. Lin, H. Wang, Wen-Li Wu, Wei Chen, and T. A. Deis. "Characterization of porous low-k dielectric thin films using X-ray reflectivity, small angle neutron scattering and ion scattering." In Proceedings of the IEEE 2001 International Interconnect Technology Conference. IEEE, 2001. http://dx.doi.org/10.1109/iitc.2001.930074.

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Reports on the topic "Small-angle X-ray and neutron scattering"

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Thomson, T. Agglomeration and Sintering in Annealed FePt Nanoparticle Assemblies Studied by Small Angle Neutron Scattering and X-Ray Diffraction. Office of Scientific and Technical Information (OSTI), January 2005. http://dx.doi.org/10.2172/839720.

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Allain, Jean Paul. Advanced grazing-emission X-ray fluorescence spectroscopy with small-angle neutron scattering for in-vivo surface composition and defect/morphology surface evolution in tokamak PMI. Office of Scientific and Technical Information (OSTI), January 2020. http://dx.doi.org/10.2172/1596402.

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Jemian, P. R., J. R. Weertman, and G. G. Long. A gradient method for anomalous small-angle x-ray scattering. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/10149708.

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Fulton, J. L., and D. M. Pfund. Small angle X-ray scattering studies of aggregation in supercritical fluid solutions. Office of Scientific and Technical Information (OSTI), October 1994. http://dx.doi.org/10.2172/10107265.

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Pfund, D. M., and J. L. Fulton. Small angle X-ray scattering studies of reverse micelles in supercritical fluids. Office of Scientific and Technical Information (OSTI), October 1994. http://dx.doi.org/10.2172/28247.

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Rice, Marybeth. Anomalous small angle x-ray scattering studies of amorphous metal-germanium alloys. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/10127769.

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Rice, M. Anomalous Small Angle X-Ray Scattering Studies of Amorphous Metal-Germanium Alloys. Office of Scientific and Technical Information (OSTI), June 2018. http://dx.doi.org/10.2172/1454109.

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Howell, Steven C. Dynamic Conformations of Nucleosome Arrays in Solution from Small-Angle X-ray Scattering. Office of Scientific and Technical Information (OSTI), January 2016. http://dx.doi.org/10.2172/1338475.

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Eliezer, D. Protein Folding and Protein Metallocluster Studies Using Synchrotron Small Angle X-Ray Scattering. Office of Scientific and Technical Information (OSTI), June 2018. http://dx.doi.org/10.2172/1454122.

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Pople, John A. Collagen Orientation and Crystallite Size in Human Dentin: A Small Angle X-ray Scattering Study. Office of Scientific and Technical Information (OSTI), March 2001. http://dx.doi.org/10.2172/784894.

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