Relevant bibliographies by topics / Langmuir Films of Perfluoroalkylalkanes

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
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Academic literature on the topic 'Langmuir Films of Perfluoroalkylalkanes'

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Published: 26 October 2024

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Journal articles on the topic "Langmuir Films of Perfluoroalkylalkanes"

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Blinov, L. M. "Langmuir films." Uspekhi Fizicheskih Nauk 155, no. 7 (1988): 443–80. http://dx.doi.org/10.3367/ufnr.0155.198807c.0443.

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Blinov, L. M. "Langmuir films." Soviet Physics Uspekhi 31, no. 7 (July 31, 1988): 623–44. http://dx.doi.org/10.1070/pu1988v031n07abeh003573.

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SUGI, Michio. "Langmuir-Blodgett Films." Nihon Kessho Gakkaishi 33, no. 3 (1991): 188–94. http://dx.doi.org/10.5940/jcrsj.33.188.

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Peterson, I. R. "Langmuir-Blodgett films." Journal of Physics D: Applied Physics 23, no. 4 (April 14, 1990): 379–95. http://dx.doi.org/10.1088/0022-3727/23/4/001.

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Mu, Jin, and Kong-Zhang Yang. "Langmuir-Blodget Films." Journal of Dispersion Science and Technology 16, no. 5 (August 1995): 333–38. http://dx.doi.org/10.1080/01932699508943687.

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Kuroda, Shin-ichi, and Michio Sugi. "Langmuir-blodgett films." Kobunshi 36, no. 4 (1987): 266–69. http://dx.doi.org/10.1295/kobunshi.36.266.

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Zasadzinski, J., R. Viswanathan, L. Madsen, J. Garnaes, and D. Schwartz. "Langmuir-Blodgett films." Science 263, no. 5154 (March 25, 1994): 1726–33. http://dx.doi.org/10.1126/science.8134836.

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Agarwal, Vijendra K. "Langmuir‐Blodgett Films." Physics Today 41, no. 6 (June 1988): 40–46. http://dx.doi.org/10.1063/1.881121.

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Collins, S. J., A. Dhathathreyan, T. Ramasami, and H. Möhwald. "Langmuir and Langmuir–Blodgett films of octadecylaminodihydroxysalicylaldehyde." Thin Solid Films 358, no. 1-2 (January 2000): 229–33. http://dx.doi.org/10.1016/s0040-6090(99)00525-8.

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Ouyang, Jian-Ming, Wei-Han Ling, Chuan Ll, Hong-Guo Liu, Qin-Bin Xue, and Gui-Ying Xu. "Langmuir and Langmuir-Blodgett Films of Bilirubin." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 363, no. 1 (July 2001): 195–205. http://dx.doi.org/10.1080/10587250108025269.

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Dissertations / Theses on the topic "Langmuir Films of Perfluoroalkylalkanes"

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Silva, Pedro Manuel Ribeiro. "Langmuir Films of Perfluoroalkylalkanes : Multiscale Insights on Molecular Structure, Mixing, and Subphase Deformability Effects." Electronic Thesis or Diss., Sorbonne université, 2024. http://www.theses.fr/2024SORUS215.

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Les perfluoroalkylalcanes (PFAA ; CnF2n+1CmH2m+1 ; FnHm) sont des molécules diblocs formées par des blocs hydrogénés (CH) et perfluorés (CF). Les deux sont hydrophobes et mutuellement phobiques. Bien qu'ils ne possèdent pas de groupe polaire, ces tensioactifs primitifs forment des films de Langmuir sur l'eau ou des substrats hydrophiles. Les films comprennent des hémimicelles monodispersées bien définies, ordonnées de manière hexagonale, comme le montrent les expériences de microscopie à force atomique (AFM) et de diffraction des rayons X à incidence rasante. Il a été observé que le diamètre de ces hémimicelles est lié à la structure moléculaire. Cependant, les effets de la structure moléculaire variable (n et/ou m), du mélange dans des films binaires et des propriétés physicochimiques de la sous-phase liquide sur la structure et l'ordre des films de Langmuir restent encore inexploités.Des études numériques préalables (simulation de dynamique moléculaire (MD)) ont élucidé la structure interne des hémimicelles F8H16 pures. Ici, les hémimicelles FnHm ont également été étudiées par MD en fonction de n et m. Il a été constaté que la disposition en éventail des molécules au sein des hémimicelles explique la variation du diamètre de l'hémimicelle avec l'architecture moléculaire, en particulier l'inadéquation des sections transversales des chaînes CH et CF et les longueurs relatives des chaînes CH. et chaînes CF. Un modèle basé sur des arguments géométriques est proposé. En outre, il a été constaté que la fosse centrale des hémimicelles mise en évidence par les mesures AFM résulte à la fois de l'interaction intermoléculaire des dipôles CH2-CF2 et de la capacité à déformer le substrat liquide. Enfin, il a été constaté que la formation d'hémimicelles ordonnées de FnHm est possible sur d'autres sous-phases liquides telles que les alcools CH et CF à chaîne courte.En outre, la structure et l'ordre des films de Langmuir mixtes F8H14: F8H20 ont été sondés par des isothermes de pression de surface et de surface moléculaire, la diffusion des rayons X aux petits angles à incidence rasante (GISAXS) et la diffraction des rayons X à incidence rasante (GIXD). Il a été constaté que le paramètre de réseau du réseau d'hémimicelles se situe entre celui des cas purs. Ceci indique soit un mélange au niveau moléculaire (formation d'hémimicelles monodispersées mixtes) soit un mélange de deux types d'hémimicelles FnHm pures.Ces résultats sont prometteurs et mettent en lumière les principes fondamentaux qui régissent l'auto-assemblage et, à terme, la prédiction et le contrôle de la morphologie des films de Langmuir nanostructurés des PFAA, envisageant leur utilisation comme modèles pour les applications de nanostructuration de surface et de nanotechnologie. Les travaux futurs devraient se concentrer sur une caractérisation plus approfondie des films binaires mixtes, y compris avec différents n et m, afin de discerner les scénarios proposés. De plus, en s'appuyant sur les connaissances accumulées, les études devraient progresser vers l'étude de films et d'émulsions mixtes de PFAA avec des biomolécules pertinentes (par exemple les phospholipides)
Perfluoroalkylalkanes (PFAAs; CnF2n+1CmH2m+1; FnHm) are diblock molecules formed by a hydrogenated (CH) and a perfluorinated (CF) blocks. Both are hydrophobic and mutually phobic. Despite lacking a polar group, these primitive surfactants form Langmuir films on water or hydrophilic substrates. The films comprise well-defined, hexagonally ordered, monodispersed hemimicelles as shown by Atomic Force Microscopy (AFM) and Grazing Incidence X-rays Diffraction experiments. It has been observed that the diameter of these hemimicelles is linked to the molecular structure. However, the effects of varying molecular structure (n and/or m), mixing in binary films and the physicochemical properties of the liquid subphase on the structure and ordering of the Langmuir films are still left untapped.Computational (Molecular Dynamics (MD) simulation) studies have elucidated the internal structure of pure F8H16 hemimicelles. Herein, FnHm hemimicelles were also studied by MD as functions of n and m. It was found that the fan-like arrangement of the molecules within the hemimicelles explains the variation of the diameter of the hemimicelle with the molecular architecture, specifically the mismatch of the CH and CF chains' cross-sectional areas and the relative lengths of the CH and CF chains. A model based on geometrical arguments is proposed. Furthermore, it was found that the central pit of the hemimicelles evidenced by AFM measurements results from both the CH2-CF2 dipoles intermolecular interaction and the ability to deform the liquid substrate. Finally, it was found that the formation of ordered hemimicelles of FnHm is possible on other liquid subphases such as short-chain CH and CF alcohols.Further, the structure and order of mixed F8H14:F8H20 Langmuir films were probed by surface pressure-molecular area isotherms, Grazing Incidence Small Angle X-Ray Scattering (GISAXS) and Grazing Incidence X-Ray Diffraction (GIXD). It was found that the lattice parameter of the network of hemimicelles is between the ones of the pure cases. This indicates either a mixing at the molecular level (formation of mixed monodisperse hemimicelles) or a mixture of two types of pure FnHm hemimicelles.These results are promising and shed light on the fundamental principles driving the self-assembling and, ultimately, the prediction and control of the morphology of the nanostructured Langmuir films of PFAAs, envisaging their use as templates for surface nanopatterning and nanotechnology applications. Future work should focus on further characterising the mixed binary films, including with different n and m, to discern between the proposed scenarios. Moreover, drawing on the accumulated knowledge, the studies should advance towards studying mixed films and emulsions of PFAAs with relevant biomolecules (e.g. phospholipids)
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Colbrook, Richard. "Pyroelectric Langmuir-Blodgett films." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.257662.

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Ou, Shih-hong. "Non-centrosymmetric Langmuir films." Case Western Reserve University School of Graduate Studies / OhioLINK, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=case1060358516.

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Yu, Lisha. "Vibrational spectroscopy of diamond films, Langmuir and Langmuir-Blodgett films and aromatic polyethers." Case Western Reserve University School of Graduate Studies / OhioLINK, 1992. http://rave.ohiolink.edu/etdc/view?acc_num=case1056553553.

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Romualdo, Torres Gemma. "Systèmes hybrides en films de Langmuir et Langmuir-Blodgett." Phd thesis, Université Sciences et Technologies - Bordeaux I, 2002. http://tel.archives-ouvertes.fr/tel-00815388.

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Ce travail porte sur la formation et la caractérisation de nouveaux systèmes organiques-inorganiques par l'utilisation de films de Langmuir et de la technique de Langmuir-Blodgett. Plusieurs voies ont ainsi été explorées afin d'obtenir des films minces hybrides aux propriétés multiples, en particulier magnétiques. L'utilisation de l'interaction entre monocouches cationiques et des anions présents en sous-phase a ainsi permis l'organisation de différents polyanions inorganiques en structure lamellaire. Cette stratégie a ensuite été généralisée au cas de colloïdes de Bleu de Prusse, composés bimétalliques étendus. Une large étude (de la préparation à la caractérisation) a été consacrée à ces matériaux mixtes Bleu de Prusse-dérivé amphiphile de Ru(bpy)3 2+. Il a été également montré que la cristallisation du Bleu de Prusse et de ses analogues est favorisée en-dessous des films de Langmuir. Finalement, la coordination d'ions dissous en sous-phase avec des molécules amphiphiles à l'interface permet d'élaborer de nouveaux systèmes pouvant former des films LB, ce qui est notamment le cas d'agencements à base de cyanures métalliques.
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Jones, Carole A. "Pyroelectricity in Langmuir-Blodgett films." Thesis, Durham University, 1987. http://etheses.dur.ac.uk/6784/.

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The fabrication of pyroelectric devices using the Langmuir-Blodgett (LB) technique is described. Studies of a wide range of materials are reported; however, the thesis concentrates on electrical and structural investigations of two specific alternate layer films: 22-tricosenoic acid/l-docosylamine and 22-tricosenoic acid/4-octadecylaniline. The latter system possesses a pyroelectric coefficient of 0.65 nCcm(^-2)K(^-1), representing the largest reported value, to date, for an LB film. The pyroelectric figure of merit (p/e(^1)(_T)) of such films is approximately 0.22 nCcm(^-2)K(^-1), which is comparable with the values for commercially available materials. The difference in pyroelectric coefficient of the two types of alternate layer film is attributed to differences in inter-layer bonding, as revealed by infrared spectroscopy. The dependence of the pyroelectric coefficients on parameters such as film thickness, substrate thickness and temperature is investigated. Structural studies, performed using electron and X-ray diffraction techniques, are also described. These provide information on the orientation of the molecules relative to the substrate and on the d-spacing of the LB films. It is shown that the substrate has a deleterious effect on the responsivity of LB film devices, and studies of films deposited onto different substrate materials indicate that there is a significant piezoelectric ally induced secondary effect contributing to the overall pyroelectric coefficient. This secondary effect is small at low temperatures, but becomes dominant at around 250 K. The results of thermally stimulated discharge experiments indicate that both free charges and dipolar groups are incorporated in the films during deposition, and become tightly bound within the polar structure.
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Amiri, M. A. "Optically nonlinear Langmuir Blodgett films." Thesis, Cranfield University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273468.

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Oliveira, Junior Osvaldo Novais de. "Electrical properties of Langmuir monolayers and deposited Langmuir-Blodgett films." Thesis, Bangor University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236716.

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Wang, Ji. "LANGMUIR LAYERS AND LANGMUIR/SCHAEFER FILMS OF BENT-CORE MOLECULES." Kent State University / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=kent1194385768.

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Constantino, Carlos José Leopoldo. "Filmes de Langmuir e Langmuir-Blodgett de ligninas." Universidade de São Paulo, 1995. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-18062008-083333/.

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Filmes de Langmuir e Langmuir-Blodgett (LB) foram fabricados a partir de ligninas de bagaço de cana-de-açúcar e da Pinus caribaea hondurensis, extraídas via processo organossolve. Obteve-se nove tipos de lignina de pinus, sendo que cada uma foi extraída com um sol vente diferente, e seis tipos de lignina de cana, as quais passaram por um fracionamento, diminuindo sua polidispersividade. Os filmes de Langmuir foram fabricados sobre subfases de água ultrapura e caracterizados por medidas de pressão e potencial de superfície. Em todos os casos constatou-se a formação de agregados não monomoleculares quando o filme é comprimido além do ponto de colapso, o que é notado pela grande histerese na isoterma pressãoárea. Para ligninas de baixa massa molecular, estruturas estáveis não monomoleculares são formadas antes do colapso. No caso das ligninas menos polidispersas (cana), a massa molecular aumenta linearmente com a área molecular média da lignina. Monocamadas das ligninas de pinus e cana puderam ser transferidas para substratos de vidro, constituindo-se nos primeiros filmes de Langmuir-Blodgett destes materiais. Através do monitoramento da velocidade de imersão e retirada do substrato da subfase pode-se fabricar diferentes tipos de filmes LB, os quais podem ser do tipo Y com a deposição ocorrendo na imersão e retirada do substrato e também dos tipos X e Z se a deposição ocorre preferencialmente na imersão ou retirada do substrato, respectivamente. Os filmes LB foram caracterizados por medidas do potencial de superfície e elipsometria. O potencial de superfície para os filmes de pinus são positivos, enquanto que para os filmes de cana são negativos. Esta inversão de sinal foi surpreendente, pois para as monocamadas os valores de potencial são sempre positivos, tanto para as ligninas de cana como para as de pinus, embora sejam maiores no caso da pinus. A razão para esta inversão é uma contribuição negativa da interface filme/substrato que suplanta a contribuição positiva dos dipolos do filme de lignina de cana. Os dados elipsométricos revelaram que a lignina apresenta um arranjo tridimensional, com muitos espaços vazios e uma espessura em torno de 60 \'angstrom\' por camada.
Langmuir monolayers and Langmuir-Blodgett (LB) films were fabricated from lignins extracted from Pinus caribaea hondurensis and sugar cane bagasse using the organosolv processo Nine types of pinus lignins were obtained by employing different solvents. The lignins of sugar cane bagasse were extracted using only one solvent but the material was fractioned into six fractions according to the molecular sizes. The resulting lignins were then less polydisperse than the pinus lignins. Langmuir monolayers were spread onto ultrapure water subphases and characterized by surface pressure and surface potential measurements. In all cases, non-monomolecular aggregates are formed when the monolayer is compressed beyond the collapse pressure, which is denoted by large hysteresis in pressurearea isotherms. For the low molecular weight lignins, stable multilayer structures are formed even before collapse. In the less polydisperse bagasse lignins, the average area per molecule increases linearly with the molecular weight. Monolayers from both pinus and bagasse lignins could be transferred onto glass substrates, thus forming the first ever reported Langmuir-Blodgett (LB) films of these materials. By controlling the dipping speed one can build-up different types of LB film which can be y-type with deposition occurring in both upstrokes and downstrokes and also Z or x-type if transfer occurs only in the upstrokes or downstrokes, respectively. The deposited LB films were characterized by surface potential and ellipsometric measurements. The surface potential of pinus films is positive whereas that of bagasse lignins is negative. This sign inversion was surprising since the monolayer surface potentials were always positive for all materials, even though they were higher for the Pinus lignins. The reason for the inversion is the negative contribution of the film/substrate interface which surpass the small, positive contribution from the dipole moments in the bagasse lignins. The ellipsometric data showed that the lignin molecules assume a three-dimensional arrangement, even within a single layer. The LB film appears to be a highly porous structure, with a thickness of 60 Á per layer.
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Books on the topic "Langmuir Films of Perfluoroalkylalkanes"

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Roberts, Gareth, ed. Langmuir-Blodgett Films. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2.

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1940-, Roberts G. G., ed. Langmuir-Blodgett films. New York: Plenum Press, 1990.

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Diniz, Jorge Manuel Boavida Fernandes. Surface thermodynamics of langmuir films for ionic langmuir-blodgett applications. Leicester: Leicester Polytechnic, 1990.

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Aspin, Ian Paul. Langmuir-Blodgett films from preformed polymers. Manchester: University of Manchester, 1992.

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Green, Christopher A. Covalent immobilisation of Langmuir-Blodgett films. Salford: University of Salford, 1993.

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Sherwin, Jennifer A. Langmuir monolayers in thin film technology. New York: Nova Science Publishers, 2011.

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Simmons, John M. Langmuir-Blodgett films of some novel phthalocyanines. Norwich: University of East Anglia, 1991.

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International Conference on Langmuir-Blodgett Films (3rd 1987 Göttingen, Germany). Langmuir-Blodgett films 3: Proceedings of the 3rd International Conference on Langmuir-Blodgett Films, Göttingen, F.R.G., July 26-31, 1987. Edited by Möbius D. London: Elsevier Applied Science, 1988.

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International Conference on Langmuir-Blodgett Films (5th 1991 Paris, France). Langmuir-Blodgett films 5: Proceedings of the 5th International Conference on Langmuir-Blodgett Films, Paris, France, August 26-30, 1991. Edited by Barraud A and Palacin S. Amsterdam: Elsevier, 1992.

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International Conference on Langmuir-Blodgett Films (4th 1989 Tsukuba Kenkyū Gakuen Toshi, Japan). Langmuir-Blodgett films 4: Proceedings of the 4th International Conference on Langmuir-Blodgett Films, Tsukuba, Japan, April 24-29, 1989. Edited by Fukuda K and Sugi M. London: Elsevier Applied Science, 1989.

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Book chapters on the topic "Langmuir Films of Perfluoroalkylalkanes"

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Hookes, D. E. "Langmuir—Blodgett Films." In Electronic Materials, 431–48. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3818-9_29.

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Hodge, P., and N. B. McKeown. "Langmuir—Blodgett films." In Principles and Applications of Nonlinear Optical Materials, 226–49. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2158-3_9.

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Ulman, Abraham. "Langmuir-Blodgett Films." In The Handbook of Surface Imaging and Visualization, 277–88. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9780367811815-22.

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Oliveira, Osvaldo N., and Diogo Volpati. "Langmuir and Langmuir–Blodgett (LB) Films." In Encyclopedia of Membranes, 1089. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_1525.

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Oliveira, Osvaldo N., and Diogo Volpati. "Langmuir and Langmuir-Blodgett (LB) Films." In Encyclopedia of Membranes, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40872-4_1525-3.

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Maganti, Lasya, Sonika Sharma, and T. P. Radhakrishnan. "Polyelectrolyte-Templated Langmuir/Langmuir–Blodgett Films." In Molecular Materials, 3–28. Boca Raton, FL : CRC Press, [2017]: CRC Press, 2017. http://dx.doi.org/10.1201/9781315118697-1.

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Giles, C. H., S. D. Forrester, and G. G. Roberts. "Historical Introduction." In Langmuir-Blodgett Films, 1–15. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_1.

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Hann, R. A. "Molecular Structure and Monolayer Properties." In Langmuir-Blodgett Films, 17–92. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_2.

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Petty, M. C., and W. A. Barlow. "Film Deposition." In Langmuir-Blodgett Films, 93–132. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_3.

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Petty, M. C. "Characterization and Properties." In Langmuir-Blodgett Films, 133–221. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_4.

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Conference papers on the topic "Langmuir Films of Perfluoroalkylalkanes"

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Neal, D. B., M. C. Petty, G. G. Roberts, M. H. Ahmad, W. J. Feast, I. R. Girling, N. A. Cade, P. V. Kolinski, and I. R. Peterson. "Langmuir-Blodgett Films for Nonlinear Optics." In Sixth IEEE International Symposium on Applications of Ferroelectrics. IEEE, 1986. http://dx.doi.org/10.1109/isaf.1986.201102.

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Lu, Xingze, and Zhi-Ming Zhang. "Langmuir-Blodgett films and nonlinear optics." In 1992 Shanghai International Symposium on Quantum Optics, edited by Yuzhu Wang, Yiqiu Wang, and Zugeng Wang. SPIE, 1992. http://dx.doi.org/10.1117/12.130461.

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Kurosawa, S. "Light emitting intelligent Langmuir-Blodgett films." In First European Conference on Smart Structures and Materials. SPIE, 1992. http://dx.doi.org/10.1117/12.2298110.

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Allen, S., T. D. McLean, P. F. Gordon, B. D. Bothwell, P. Robin, and I. Ledoux. "Properties Of Polyenic Langmuir Blodgett Films." In 32nd Annual Technical Symposium, edited by Garo Khanarian. SPIE, 1988. http://dx.doi.org/10.1117/12.948234.

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Zanoni, R., C. Naselli, J. Bell, G. Stegeman, and C. Seaton. "Brillouin spectra of Langmuir-Blodgett films." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1985. http://dx.doi.org/10.1364/oam.1985.thv8.

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The Brillouin spectra of thin films of cadmium arachidate have been measured. These films are multiple layers of ordered monolayers (26.8 Å thick) of the cadmium salt of arachidic acid deposited one monolayer at a time onto aluminum and glass substrates by the Langmuir-Blodgett technique.1 The elastic properties of these films can be determined from these Brillouin scattering spectra. Light from a single-mode argon-ion laser at 0.5145 m was scattered by multiple, high frequency, surface acoustic waves guided by LB films of thickness 100, 35, and 11 monolayers. The scattered light was collected and spectrum analyzed with a 9-pass tandem Fabry-Perot interferometer to obtain the velocities of the surface acoustic waves. The use of the tandem interferometer provided the high contrast needed to detect the weak Brillouin signals in the presence of the intense elastically scattered light. The Brillouin spectra are now being analyzed to determine the elastic properties of the Langmuir-Blodgett films.
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Gaididei, Yu B., and A. S. Trofimov. "Photorefractive Effects in Langmuir-Blodgett Films." In Photorefractive Materials, Effects, and Devices II. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/pmed.1993.frh.9.

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Martynski, Tomasz, Andrezj Biadasz, Robert Hertmanowski, and Danuta Bauman. "Fluorescent dyes mixed with liquid crystals in Langmuir and Langmuir-Blodgett films." In SPIE Proceedings, edited by Jozef Zmija. SPIE, 2004. http://dx.doi.org/10.1117/12.581134.

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Mattoso, L. H. C., S. V. Mello, A. Riul, G. D. Telles, and O. N. Oliveira. "Langmuir and Langmuir-Blodgett films of parent polyaniline doped with functionalized acids." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835767.

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Olsen, Eric, Rajesh Guntupalli, Iryna Sorkulova, Robert Long, William Neely, and Vitaly Vodyanoy. "Phage Langmuir-Blodgett films for biosensing applications." In 2010 Ninth IEEE Sensors Conference (SENSORS 2010). IEEE, 2010. http://dx.doi.org/10.1109/icsens.2010.5690208.

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ZHAVNERKO, G. K., I. V. PARIBOK, V. E. AGABEKOV, SOLIMAN H. AL-KHOWAITER, and MUHANNA K. A. ALMUHANNA. "MAGNETIC LANGMUIR-BLODGETT FILMS WITH GLUING PROPERTIES." In Proceedings of International Conference Nanomeeting – 2011. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814343909_0084.

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Reports on the topic "Langmuir Films of Perfluoroalkylalkanes"

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Mirley, C. L., and J. T. Koberstein. Tribology of Langmuir-Blodgett Films. Fort Belvoir, VA: Defense Technical Information Center, March 1992. http://dx.doi.org/10.21236/ada250075.

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Rahman, A. K., L. Samuelson, D. Minehan, S. Clough, S. Tripathy, T. Inagaki, X. O. Yang, T. A. Skotheim, and Y. Okamoto. Ordered Langmuir-Blodgett Films of Polypyrrole and Analogs. Fort Belvoir, VA: Defense Technical Information Center, October 1988. http://dx.doi.org/10.21236/ada200615.

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Duran, R. S., W. Sigmund, T. Bailey, and M. Hara. Langmuir Blodgett and STM Investigations of Conducting Polymer Thin Films. Fort Belvoir, VA: Defense Technical Information Center, December 1993. http://dx.doi.org/10.21236/ada274512.

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Vlakhov, Todor, George Ivanov, and George Hadjichristov. Phospholipid Langmuir-Blodgett Films and Impedance Spectroscopy for Detection of Acetone and Methanol Vapours. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, June 2021. http://dx.doi.org/10.7546/crabs.2021.06.04.

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Cesarano, J. III. Modeling and characterization of molecular structures in self assembled and Langmuir-Blodgett films for controlled fabrication. Office of Scientific and Technical Information (OSTI), October 1997. http://dx.doi.org/10.2172/548662.

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You might also be interested in the extended bibliographies on the topic 'Langmuir Films of Perfluoroalkylalkanes' for particular source types:
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