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Journal articles on the topic 'SANS a SAXS'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Metwalli, Ezzeldin, Klaus Götz, Tobias Zech, Christian Bär, Isabel Schuldes, Anne Martel, Lionel Porcar, and Tobias Unruh. "Simultaneous SAXS/SANS Method at D22 of ILL: Instrument Upgrade." Applied Sciences 11, no. 13 (June 25, 2021): 5925. http://dx.doi.org/10.3390/app11135925.

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A customized portable SAXS instrument has recently been constructed, installed, and tested at the D22 SANS instrument at ILL. Technical characteristics of this newly established plug-and-play SAXS system have recently been reported (J. Appl. Cryst. 2020, 53, 722). An optimized lead shielding arrangement on the SAXS system and a double energy threshold X-ray detector have been further implemented to substantially suppress the unavoidable high-energy gamma radiation background on the X-ray detector. The performance of the upgraded SAXS instrument has been examined systematically by determining background suppression factors (SFs) at various experimental conditions, including different neutron beam collimation lengths and X-ray sample-to-detector distances (SDDX-ray). Improved signal-to-noise ratio SAXS data enables combined SAXS and SANS measurements for all possible experimental conditions at the D22 instrument. Both SAXS and SANS data from the same sample volume can be fitted simultaneously using a common structural model, allowing unambiguous interpretation of the scattering data. Importantly, advanced in situ/real time investigations are possible, where both the SAXS and the SANS data can reveal time-resolved complementary nanoscale structural information.

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2

GOYAL, P. S., and V. K. ASWAL. "USE OF SANS AND SAXS IN STUDY OF NANOPARTICLES." International Journal of Nanoscience 04, no. 05n06 (October 2005): 987–94. http://dx.doi.org/10.1142/s0219581x05003954.

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Small Angle Neutron Scattering (SANS) and Small Angle X-ray Scattering (SAXS), anong other available techniques, are the nost sought after techniques for studying the sizes and shapes of nanoparticles. The contrast between particle and its surrounding is different for X-rays and neutrons. Thus a combined SANS and SAXS study, at times, provides information about the core and the shell structure of nanoparticles. This paper gives an introduction to the techniques of SANS and SAXS and shows results of a study of core-shell structure for a micelle (nanaoparticle of organic material).

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3

Sato, Nobuhiro, Rina Yogo, Saeko Yanaka, Anne Martel, Lionel Porcar, Ken Morishima, Rintaro Inoue, et al. "A feasibility study of inverse contrast-matching small-angle neutron scattering method combined with size exclusion chromatography using antibody interactions as model systems." Journal of Biochemistry 169, no. 6 (February 2, 2021): 701–8. http://dx.doi.org/10.1093/jb/mvab012.

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Abstract Small-angle neutron scattering (SANS) and small- angle X-ray scattering (SAXS) are powerful techniques for the structural characterization of biomolecular complexes. In particular, SANS enables a selective observation of specific components in complexes by selective deuteration with contrast-matching techniques. In most cases, however, biomolecular interaction systems with heterogeneous oligomers often contain unfavorable aggregates and unbound species, hampering data interpretation. To overcome these problems, SAXS has been recently combined with size exclusion chromatography (SEC), which enables the isolation of the target complex in a multi-component system. By contrast, SEC–SANS is only at a preliminary stage. Hence, we herein perform a feasibility study of this method based on our newly developed inverse contrast-matching (iCM) SANS technique using antibody interactions as model systems. Immunoglobulin G (IgG) or its Fc fragment was mixed with 75% deuterated Fc-binding proteins, i.e. a mutated form of IgG-degrading enzyme of Streptococcus pyogenes and a soluble form of Fcγ receptor IIIb, and subjected to SEC–SANS as well as SEC–SAXS as reference. We successfully observe SANS from the non-deuterated IgG or Fc formed in complex with these binding partners, which were unobservable in terms of SANS in D2O, hence demonstrating the potential utility of the SEC–iCM–SANS approach.

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4

Ballauff, M. "SAXS and SANS studies of polymer colloids." Current Opinion in Colloid & Interface Science 6, no. 2 (May 2001): 132–39. http://dx.doi.org/10.1016/s1359-0294(01)00072-3.

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5

Smarsly, B. M., S. Mascotto, C. Weidmann, and H. Kaper. "Charakterisierung mesoporöser Materialien mittels Kleinwinkelstreuung (SAXS/SANS)." Chemie Ingenieur Technik 82, no. 6 (June 2010): 823–28. http://dx.doi.org/10.1002/cite.201000075.

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6

Demé, Bruno. "SAXS and SANS techniques discussed in Grenoble." Neutron News 10, no. 3 (January 1999): 15. http://dx.doi.org/10.1080/10448639908233682.

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7

Johansen, Nicolai Tidemand, Martin Cramer Pedersen, Lionel Porcar, Anne Martel, and Lise Arleth. "Introducing SEC–SANS for studies of complex self-organized biological systems." Acta Crystallographica Section D Structural Biology 74, no. 12 (November 30, 2018): 1178–91. http://dx.doi.org/10.1107/s2059798318007180.

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Small-angle neutron scattering (SANS) is maturing as a method for studying complex biological structures. Owing to the intrinsic ability of the technique to discern between 1H- and 2H-labelled particles, it is especially useful for contrast-variation studies of biological systems containing multiple components. SANS is complementary to small-angle X-ray scattering (SAXS), in which similar contrast variation is not easily performed but in which data with superior counting statistics are more easily obtained. Obtaining small-angle scattering (SAS) data on monodisperse complex biological structures is often challenging owing to sample degradation and/or aggregation. This problem is enhanced in the D2O-based buffers that are typically used in SANS. In SAXS, such problems are solved using an online size-exclusion chromatography (SEC) setup. In the present work, the feasibility of SEC–SANS was investigated using a series of complex and difficult samples of membrane proteins embedded in nanodisc particles that consist of both phospholipid and protein components. It is demonstrated that SEC–SANS provides data of sufficient signal-to-noise ratio for these systems, while at the same time circumventing aggregation. By combining SEC–SANS and SEC–SAXS data, an optimized basis for refining structural models of the investigated structures is obtained.

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8

KANAYA, Toshiji, Nobuaki TAKAHASHI, Rintaro INOUE, Koji NISHIDA, and Go MATSUBA. "Flow and Deformation-induced Polymer Crystallization by SANS and SAXS." Nihon Kessho Gakkaishi 57, no. 1 (2015): 27–33. http://dx.doi.org/10.5940/jcrsj.57.27.

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9

Allen, A. "SAXS and SANS for industrial materials-by-design." Acta Crystallographica Section A Foundations of Crystallography 67, a1 (August 22, 2011): C29—C30. http://dx.doi.org/10.1107/s0108767311099399.

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10

Kajiwara, Kanji. "Structural Characterization of Gels by SAXS and SANS." Kobunshi 42, no. 7 (1993): 600–603. http://dx.doi.org/10.1295/kobunshi.42.600.

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11

Lou, Kuo-Long, Po-Tsang Huang, Guey-Yueh Shi, and Hua-Lin Wu. "SAXS/SANS structural analysis of human thrombomodulin domains." Acta Crystallographica Section A Foundations of Crystallography 65, a1 (August 16, 2009): s335—s336. http://dx.doi.org/10.1107/s0108767309092836.

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12

Grillo, Isabelle. "Applications of stopped-flow in SAXS and SANS." Current Opinion in Colloid & Interface Science 14, no. 6 (December 2009): 402–8. http://dx.doi.org/10.1016/j.cocis.2009.04.005.

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13

Metwalli, Ezzeldin, Klaus Götz, Sebastian Lages, Christian Bär, Tobias Zech, Dennis M. Noll, Isabel Schuldes, et al. "A novel experimental approach for nanostructure analysis: simultaneous small-angle X-ray and neutron scattering." Journal of Applied Crystallography 53, no. 3 (May 13, 2020): 722–33. http://dx.doi.org/10.1107/s1600576720005208.

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Exploiting small-angle X-ray and neutron scattering (SAXS/SANS) on the same sample volume at the same time provides complementary nanoscale structural information in two different contrast situations. Unlike an independent experimental approach, the truly combined SAXS/SANS experimental approach ensures the exactness of the probed samples, particularly for in situ studies. Here, an advanced portable SAXS system that is dimensionally suitable for installation in the D22 zone of ILL is introduced. The SAXS apparatus is based on a Rigaku switchable copper/molybdenum microfocus rotating-anode X-ray generator and a DECTRIS detector with a changeable sample-to-detector distance of up to 1.6 m in a vacuum chamber. A case study is presented to demonstrate the uniqueness of the newly established method. Temporal structural rearrangements of both the organic stabilizing agent and organically capped gold colloidal particles during gold nanoparticle growth are simultaneously probed, enabling the immediate acquisition of correlated structural information. The new nano-analytical method will open the way for real-time investigations of a wide range of innovative nanomaterials and will enable comprehensive in situ studies on biological systems. The potential development of a fully automated SAXS/SANS system with a common control environment and additional sample environments, permitting a continual and efficient operation of the system by ILL users, is also introduced.

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14

Lamparter, P., and B. Boucher. "Small Angle Neutron Scattering with Hydrogenated Amorphous Cu50 Ti50 and Ni-Ti-Si Alloys." Zeitschrift für Naturforschung A 48, no. 11 (November 1, 1993): 1086–92. http://dx.doi.org/10.1515/zna-1993-1105.

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Abstract The metallic glasses Cu50Ti50, Ni30Ti60Si10, Ni32Ti52Si16 , Ni16Ti68Si16 and Ti84Si16 were produced by melt spinning. The alloys in the blank state as well as after loading with hydrogen or deuterium were investigated by small angle neutron (SANS) and X-ray (SAXS) scattering. The scattering of the different amorphous alloys exhibited common features. SANS follows a power-law with exponent of the scattering vector between -3 and -4. The melt-spun glasses contain extended structural inhomogeneities which are associated rather with the local composition than with the local density. SAXS measurements did not show effects above the background level. Loading the alloys with hydrogen or deuterium causes strong effects in the SANS behaviour. From the results it is concluded that the amorphous alloys contain inner surfaces where the hydrogen atoms segregate.

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15

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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16

Hasegawa, H., H. Tanaka, T. Hashimoto, and C. C. Han. "SANS and SAXS study of block copolymer/homopolymer mixtures." Journal of Applied Crystallography 24, no. 5 (October 1, 1991): 672–78. http://dx.doi.org/10.1107/s0021889890014212.

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17

Ryan, A. J., S. Naylor, N. J. Terrill, and S. King. "Chain Conformations in Polyurethanes: A SAXS & SANS Study." Fibre Diffraction Review 5, no. 5 (1996): 38. http://dx.doi.org/10.1382/s19960538.

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18

Madl, Tobias. "Integration von NMR und SAXS/SANS in der Strukturbiologie." BIOspektrum 19, no. 4 (June 2013): 386–89. http://dx.doi.org/10.1007/s12268-013-0327-8.

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19

Zabelskii, D. V., A. V. Vlasov, Yu L. Ryzhykau, T. N. Murugova, M. Brennich, D. V. Soloviov, O. I. Ivankov, et al. "Ambiguities and completeness of SAS data analysis: investigations of apoferritin by SAXS/SANS EID and SEC-SAXS methods." Journal of Physics: Conference Series 994 (March 2018): 012017. http://dx.doi.org/10.1088/1742-6596/994/1/012017.

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20

Hollamby, Martin J., Catherine F. Smith, Melanie M. Britton, Ashleigh E. Danks, Zoe Schnepp, Isabelle Grillo, Brian R. Pauw, Akihiro Kishimura, and Takashi Nakanishi. "The aggregation of an alkyl–C60 derivative as a function of concentration, temperature and solvent type." Physical Chemistry Chemical Physics 20, no. 5 (2018): 3373–80. http://dx.doi.org/10.1039/c7cp06348b.

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21

Allen, Andrew J., Fan Zhang, R. Joseph Kline, William F. Guthrie, and Jan Ilavsky. "NIST Standard Reference Material 3600: Absolute Intensity Calibration Standard for Small-Angle X-ray Scattering." Journal of Applied Crystallography 50, no. 2 (March 7, 2017): 462–74. http://dx.doi.org/10.1107/s1600576717001972.

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The certification of a new standard reference material for small-angle scattering [NIST Standard Reference Material (SRM) 3600: Absolute Intensity Calibration Standard for Small-Angle X-ray Scattering (SAXS)], based on glassy carbon, is presented. Creation of this SRM relies on the intrinsic primary calibration capabilities of the ultra-small-angle X-ray scattering technique. This article describes how the intensity calibration has been achieved and validated in the certifiedQrange,Q= 0.008–0.25 Å−1, together with the purpose, use and availability of the SRM. The intensity calibration afforded by this robust and stable SRM should be applicable universally to all SAXS instruments that employ a transmission measurement geometry, working with a wide range of X-ray energies or wavelengths. The validation of the SRM SAXS intensity calibration using small-angle neutron scattering (SANS) is discussed, together with the prospects for including SANS in a future renewal certification.

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22

Butter, Karen, Armin Hoell, Albrecht Wiedenmann, Andrei V. Petukhov, and Gert-Jan Vroege. "Small-angle neutron and X-ray scattering of dispersions of oleic-acid-coated magnetic iron particles." Journal of Applied Crystallography 37, no. 6 (November 11, 2004): 847–56. http://dx.doi.org/10.1107/s0021889804018564.

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This paper describes the characterization of dispersions of oleic-acid-coated magnetic iron particles by small-angle neutron and X-ray scattering (SANS and SAXS). Both oxidized and non-oxidized dilute samples were studied by SANS at different contrasts. The non-oxidized samples are found to consist of non-interacting superparamagnetic single dipolar particles, with a lognormal distribution of iron cores, surrounded by a surfactant shell, which is partially penetrated by solvent. This model is supported by SAXS measurements on the same dispersion. Small iron particles are expected to oxidize upon exposure to air. SANS was used to study the effect of this oxidation, both on single particles, as well as on interparticle interactions. It is found that on exposure to air, a non-magnetic oxide layer is formed around the iron cores, which causes an increase of particle size. In addition, particles are found to aggregate upon oxidation, presumably because the surfactant density on the particle surfaces is decreased.

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23

Izumi, Atsushi. "Structural Analysis of Phenolic Resin Moldings Using SAXS and SANS." Seikei-Kakou 26, no. 10 (September 20, 2014): 464–67. http://dx.doi.org/10.4325/seikeikakou.26.464.

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24

Nozue, Y., M. Shibayama, E. B. Coughlin, and J. A. Kornfield. "SAXS and SANS for the better understanding of polymer processing." Acta Crystallographica Section A Foundations of Crystallography 67, a1 (August 22, 2011): C235. http://dx.doi.org/10.1107/s0108767311094128.

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25

Wu, Guangwei, Lizhi Liu, Vinh-Bao Buu, Benjamin Chu, and Dieter K. Schneider. "SANS and SAXS studies of pluronic L64 in concentrated solution." Physica A: Statistical Mechanics and its Applications 231, no. 1-3 (September 1996): 73–81. http://dx.doi.org/10.1016/0378-4371(95)00445-9.

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26

Zhou, Huan-Xiang, and Osman Bilsel. "SAXS/SANS Probe of Intermolecular Interactions in Concentrated Protein Solutions." Biophysical Journal 106, no. 4 (February 2014): 771–73. http://dx.doi.org/10.1016/j.bpj.2014.01.019.

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27

Golub, Maksym, Adrian Kölsch, Artem Feoktystov, Athina Zouni, and Jörg Pieper. "Insights into Solution Structures of Photosynthetic Protein Complexes from Small-Angle Scattering Methods." Crystals 11, no. 2 (February 19, 2021): 203. http://dx.doi.org/10.3390/cryst11020203.

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High-resolution structures of photosynthetic pigment–protein complexes are often determined using crystallography or cryo-electron microscopy (cryo-EM), which are restricted to the use of protein crystals or to low temperatures, respectively. However, functional studies and biotechnological applications of photosystems necessitate the use of proteins isolated in aqueous solution, so that the relevance of high-resolution structures has to be independently verified. In this regard, small-angle neutron and X-ray scattering (SANS and SAXS, respectively) can serve as the missing link because of their capability to provide structural information for proteins in aqueous solution at physiological temperatures. In the present review, we discuss the principles and prototypical applications of SANS and SAXS using the photosynthetic pigment–protein complexes phycocyanin (PC) and Photosystem I (PSI) as model systems for a water-soluble and for a membrane protein, respectively. For example, the solution structure of PSI was studied using SAXS and SANS with contrast matching. A Guinier analysis reveals that PSI in solution is virtually free of aggregation and characterized by a radius of gyration of about 75 Å. The latter value is about 10% larger than expected from the crystal structure. This is corroborated by an ab initio structure reconstitution, which also shows a slight expansion of Photosystem I in buffer solution at room temperature. In part, this may be due to conformational states accessible by thermally activated protein dynamics in solution at physiological temperatures. The size of the detergent belt is derived by comparison with SANS measurements without detergent match, revealing a monolayer of detergent molecules under proper solubilization conditions.

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28

Toolan, Daniel T. W., Michael P. Weir, Rachel C. Kilbride, Jon R. Willmott, Stephen M. King, James Xiao, Neil C. Greenham, et al. "Controlling the structures of organic semiconductor–quantum dot nanocomposites through ligand shell chemistry." Soft Matter 16, no. 34 (2020): 7970–81. http://dx.doi.org/10.1039/d0sm01109f.

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Structural insights via small angle X-ray and neutron (SAXS and SANS, respectively) into how nanocrystal quantum dots (QD) functionalized with organic ligands self-assemble with a small molecule organic semiconductor.

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29

Skoglund, Sara, Eva Blomberg, Inger Odnevall Wallinder, Isabelle Grillo, Jan Skov Pedersen, and L. Magnus Bergström. "A novel explanation for the enhanced colloidal stability of silver nanoparticles in the presence of an oppositely charged surfactant." Phys. Chem. Chem. Phys. 19, no. 41 (2017): 28037–43. http://dx.doi.org/10.1039/c7cp04662f.

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The structural behavior in aqueous mixtures of negatively charged silver nanoparticles (Ag NPs) together with the cationic surfactants cetyltrimethylammonium bromide (CTAB) and dodecyltrimethylammonium chloride (DTAC), respectively, has been investigated using SANS and SAXS.

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30

Sreij, Ramsia, Carina Dargel, Philippe Geisler, Yvonne Hertle, Aurel Radulescu, Stefano Pasini, Javier Perez, Lara H. Moleiro, and Thomas Hellweg. "DMPC vesicle structure and dynamics in the presence of low amounts of the saponin aescin." Physical Chemistry Chemical Physics 20, no. 14 (2018): 9070–83. http://dx.doi.org/10.1039/c7cp08027a.

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Vesicle shape and bilayer parameters are studied by small-angle X-ray (SAXS) and small-angle neutron (SANS) scattering in the presence of the saponin aescin. Bilayer dynamics is studied by neutron spin-echo (NSE) spectroscopy.

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31

Semeraro, Enrico F., Juliette M. Devos, Lionel Porcar, V. Trevor Forsyth, and Theyencheri Narayanan. "In vivoanalysis of theEscherichia coliultrastructure by small-angle scattering." IUCrJ 4, no. 6 (September 26, 2017): 751–57. http://dx.doi.org/10.1107/s2052252517013008.

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The flagellated Gram-negative bacteriumEscherichia coliis one of the most studied microorganisms. Despite extensive studies as a model prokaryotic cell, the ultrastructure of the cell envelope at the nanometre scale has not been fully elucidated. Here, a detailed structural analysis of the bacterium using a combination of small-angle X-ray and neutron scattering (SAXS and SANS, respectively) and ultra-SAXS (USAXS) methods is presented. A multiscale structural model has been derived by incorporating well established concepts in soft-matter science such as a core-shell colloid for the cell body, a multilayer membrane for the cell wall and self-avoiding polymer chains for the flagella. The structure of the cell envelope was resolved by constraining the model by five different contrasts from SAXS, and SANS at three contrast match points and full contrast. This allowed the determination of the membrane electron-density profile and the inter-membrane distances on a quantitative scale. The combination of USAXS and SAXS covers size scales from micrometres down to nanometres, enabling the structural elucidation of cells from the overall geometry down to organelles, thereby providing a powerful method for a non-invasive investigation of the ultrastructure. This approach may be applied for probingin vivothe effect of detergents, antibiotics and antimicrobial peptides on the bacterial cell wall.

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32

Izumi, Atsushi, Toshio Nakao, Hiroki Iwase, and Mitsuhiro Shibayama. "Structural Analysis of Cured Phenolic Resins using Complementary SANS and SAXS." hamon 24, no. 1 (2014): 11–14. http://dx.doi.org/10.5611/hamon.24.1_11.

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33

Triolo, A., J. S. Lin, and R. Triolo. "Combined SANS and SAXS experiments in polyolefins-hydrogenated oligocyclopentadiene (HOCP) blends." Physica A: Statistical Mechanics and its Applications 249, no. 1-4 (January 1998): 362–68. http://dx.doi.org/10.1016/s0378-4371(97)00492-5.

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34

Jenkins, Paul J., and Athene M. Donald. "Gelatinisation of starch: a combined SAXS/WAXS/DSC and SANS study." Carbohydrate Research 308, no. 1-2 (March 1998): 133–47. http://dx.doi.org/10.1016/s0008-6215(98)00079-2.

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35

Sugiyama, Masaaki, Norihiko Fujii, Yukio Morimoto, Keiji Itoh, Kazuhiro Mori, Toshiharu Fukunaga, and Noriko Fujii. "SAXS and SANS Observations of Abnormal Aggregation of Human α-Crystallin." Chemistry & Biodiversity 7, no. 6 (June 16, 2010): 1380–88. http://dx.doi.org/10.1002/cbdv.200900332.

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36

Hoell, A., A. Heinemann, M. Kammel, and A. Wiedenmann. "Nanostructure and ordering in magnetic liquids probed by SAXS and SANS." Acta Crystallographica Section A Foundations of Crystallography 61, a1 (August 23, 2005): c74. http://dx.doi.org/10.1107/s0108767305096868.

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37

Joshi, J. V., V. K. Aswal, and P. S. Goyal. "Combined SANS and SAXS studies on alkali metal dodecyl sulphate micelles." Journal of Physics: Condensed Matter 19, no. 19 (April 20, 2007): 196219. http://dx.doi.org/10.1088/0953-8984/19/19/196219.

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38

Murthy, N. Sanjeeva, Zheng Zhang, Siddharth Borsadia, and Joachim Kohn. "Nanospheres with a smectic hydrophobic core and an amorphous PEG hydrophilic shell: structural changes and implications for drug delivery." Soft Matter 14, no. 8 (2018): 1327–35. http://dx.doi.org/10.1039/c7sm02472j.

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The structural changes in nanospheres with a crystalline core and an amorphous diffuse shell were investigated by small-angle neutron scattering (SANS), small-, medium-, and wide-angle X-ray scattering (SAXS, MAXS and WAXS), and differential scanning calorimetry (DSC).

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39

Vass, Sz, J. Pleštil, P. Laggner, S. Borbély, H. Pospı́šil, and T. Gilányi. "Simultaneous evaluation of SAXS and SANS patterns from solutions of ionic micelles." Physica B: Condensed Matter 276-278 (March 2000): 406–7. http://dx.doi.org/10.1016/s0921-4526(99)01505-7.

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40

Manet, Sabine, Anne-Sophie Cuvier, Claire Valotteau, Giulia C. Fadda, Javier Perez, Esra Karakas, Stéphane Abel, and Niki Baccile. "Structure of Bolaamphiphile Sophorolipid Micelles Characterized with SAXS, SANS, and MD Simulations." Journal of Physical Chemistry B 119, no. 41 (October 2, 2015): 13113–33. http://dx.doi.org/10.1021/acs.jpcb.5b05374.

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41

Morfin, Isabelle, Françoise Ehrburger-Dolle, Isabelle Grillo, Frédéric Livet, and Françoise Bley. "ASAXS, SAXS and SANS investigations of vulcanized elastomers filled with carbon black." Journal of Synchrotron Radiation 13, no. 6 (October 18, 2006): 445–52. http://dx.doi.org/10.1107/s090904950603425x.

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42

Filippov, Sergey K., John M. Franklin, Petr V. Konarev, Petr Chytil, Tomas Etrych, Anna Bogomolova, Margarita Dyakonova, et al. "Hydrolytically Degradable Polymer Micelles for Drug Delivery: A SAXS/SANS Kinetic Study." Biomacromolecules 14, no. 11 (October 25, 2013): 4061–70. http://dx.doi.org/10.1021/bm401186z.

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43

Kalus, J., and U. Schmelzer. "Small angle neutron (SANS) and x-ray (SAXS) scattering on micellar systems." Physica Scripta T49B (January 1, 1993): 629–35. http://dx.doi.org/10.1088/0031-8949/1993/t49b/042.

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Botti, A., W. Pyckhout-Hintzen, D. Richter, and E. Straube. "Filled elastomers: polymer chain and filler characterization by a SANS–SAXS approach." Physica A: Statistical Mechanics and its Applications 304, no. 1-2 (February 2002): 230–34. http://dx.doi.org/10.1016/s0378-4371(01)00512-x.

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Larson-Smith, Kjersta, Andrew Jackson, and Danilo C. Pozzo. "SANS and SAXS Analysis of Charged Nanoparticle Adsorption at Oil–Water Interfaces." Langmuir 28, no. 5 (January 26, 2012): 2493–501. http://dx.doi.org/10.1021/la204513n.

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Jouault, Nicolas, Rémi Nguyen, Michel Rawiso, Nicolas Giuseppone, and Eric Buhler. "SANS, SAXS, and light scattering investigations of pH-responsive dynamic combinatorial mesophases." Soft Matter 7, no. 10 (2011): 4787. http://dx.doi.org/10.1039/c1sm05164d.

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Sartori, Sabrina, Kenneth D. Knudsen, Zhirong Zhao-Karger, Elisa Gil Bardaji, Jiri Muller, Maximilian Fichtner, and Bjørn C. Hauback. "Nanoconfined Magnesium Borohydride for Hydrogen Storage Applications Investigated by SANS and SAXS." Journal of Physical Chemistry C 114, no. 44 (October 18, 2010): 18785–89. http://dx.doi.org/10.1021/jp1058726.

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Uhríková, D., M. Hanulová, N. Kucerka, A. Islamov, S. S. Funari, and P. Balgavý. "The structure of DNA+cationic liposome aggregates studied using SAXS and SANS." Acta Crystallographica Section A Foundations of Crystallography 61, a1 (August 23, 2005): c73. http://dx.doi.org/10.1107/s0108767305096881.

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Huang, P. T., K. L. Lou, G. Y. Shi, and H. L. Hu. "Crystal structural determination and SAXS/SANS structural analysis of human thrombomodulin domains." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (August 23, 2008): C470. http://dx.doi.org/10.1107/s0108767308084894.

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Cherniavskyi, Yevhen K., and D. Peter Tieleman. "Lipid Bilayer Structure Refinement with Saxs/Sans Based Restrained Ensemble Molecular Dynamics." Biophysical Journal 116, no. 3 (February 2019): 164a. http://dx.doi.org/10.1016/j.bpj.2018.11.912.

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