Relevant bibliographies by topics / Non-polar

Contents

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

Academic literature on the topic 'Non-polar'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Non-polar"

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J K Pendharkar, J. K. Pendharkar, and Veena Khilnani. "Acoustic Parameters of Polar- Non polar Chemicals at Variable Frequencies." Indian Journal of Applied Research 3, no. 7 (October 1, 2011): 588–90. http://dx.doi.org/10.15373/2249555x/july2013/186.

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Ahmed, Hameed M., and Shuja-Aldeen B. Aziz. "Dielectric Properties of Commercial non-Polar Polymers." Journal of Zankoy Sulaimani - Part A 11, no. 1 (April 10, 2008): 1–8. http://dx.doi.org/10.17656/jzs.10175.

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Boytsova, O., I. Dovgaliuk, D. Chernyshov, A. Eliseev, P. O'Brien, A. J. Sutherland, and A. Bosak. "Polar and non-polar structures of NH4TiOF3." Journal of Applied Crystallography 52, no. 1 (February 1, 2019): 23–26. http://dx.doi.org/10.1107/s1600576718016606.

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Ammonium oxofluorotitanate, NH4TiOF3, is probably the best known precursor for the synthesis of anatase mesocrystals. Transformation of NH4TiOF3 into TiO2 through thermal decomposition, accompanied by hydrolysis, preserves some structural features of the precursor. Currently, any discussion of the mechanism of this transformation is difficult, as the exact crystal structure of the starting compound is not available and no intermediate structures are known. This article describes the outcome of single-crystal and powder X-ray diffraction studies, revealing the existence of two polymorphs of the parent NH4TiOF3 at different temperatures. A second-order phase transition from the polar Pca21 α phase (1), stable at room temperature, to the Pma2 β phase (2) above ∼433 K has been demonstrated. The direction of the pseudo-fourfold axis in NH4TiOF3 coincides with the orientation of the fourfold axis of anatase mesocrystals, consistent with a topotactical transformation.
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Dongmo Foumthuim, Cedrix J., Manuel Carrer, Maurine Houvet, Tatjana Škrbić, Giuseppe Graziano, and Achille Giacometti. "Can the roles of polar and non-polar moieties be reversed in non-polar solvents?" Physical Chemistry Chemical Physics 22, no. 44 (2020): 25848–58. http://dx.doi.org/10.1039/d0cp02948c.

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Using thermodynamic integration, we study the solvation free energy of 18 amino acid side chain equivalents in solvents with different polarities, ranging from the most polar water to the most non-polar cyclohexane.
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Omini, M. "Permittivity of Polar Solutions in Non-Polar Solvents." IEEE Transactions on Electrical Insulation EI-20, no. 6 (December 1985): 965–73. http://dx.doi.org/10.1109/tei.1985.348737.

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Kucharski, R., M. Zając, R. Doradziński, M. Rudziński, R. Kudrawiec, and R. Dwiliński. "Non-polar and semi-polar ammonothermal GaN substrates." Semiconductor Science and Technology 27, no. 2 (January 19, 2012): 024007. http://dx.doi.org/10.1088/0268-1242/27/2/024007.

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Mahmoudinobar, Farbod, Zhaoqian Su, and Cristiano L. Dias. "Thermodynamic Stability of Polar and Non-polar Fibrils." Biophysical Journal 114, no. 3 (February 2018): 414a. http://dx.doi.org/10.1016/j.bpj.2017.11.2295.

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Engelhardt, H., R. Grüner, and M. Scherer. "The polar selectivities of non-polar reversed phases." Chromatographia 53, S1 (January 2001): S154—S161. http://dx.doi.org/10.1007/bf02490322.

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Kim, Kwang Soo, Kwang Ho Ahn, Jae Ro Park, and Hyun Jung Kim. "Development of Cellulosic Fiber Filter Using Replacement Liquid in Water-Swollen Fiber with Non-Polar Solvent." Journal of Korean Society of Environmental Engineers 35, no. 10 (October 30, 2013): 743–48. http://dx.doi.org/10.4491/ksee.2013.35.10.743.

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Pykacz, Henryk, and Zbigniew Czapla. "Coexistence of polar and non-polar phases in ND4DSeO4crystals." Ferroelectrics Letters Section 7, no. 3 (May 1987): 61–65. http://dx.doi.org/10.1080/07315178708200516.

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Dissertations / Theses on the topic "Non-polar"

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Newsham, David K. Sen Ayusman. "Palladium catalyzed copolymerizations of polar and non-polar monomers." [University Park, Pa.] : Pennsylvania State University, 2009. http://etda.libraries.psu.edu/theses/approved/WorldWideIndex/ETD-4528/index.html.

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Hanan, Faridah Hanim Ab. "Plasticizer transportation studies in polar and non-polar rubbers." Thesis, London Metropolitan University, 2001. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341733.

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SILVA, ELIZANDRA MARTINS. "NANOSCALE MECHANICAL DEFORMATION MECHANISMS OF POLAR AND NON-POLAR ZNO." PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO, 2014. http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=24779@1.

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PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO
COORDENAÇÃO DE APERFEIÇOAMENTO DO PESSOAL DE ENSINO SUPERIOR
CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO
PROGRAMA DE SUPORTE À PÓS-GRADUAÇÃO DE INSTS. DE ENSINO
Neste trabalho foi estudado o mecanismo de deformação de faces polares e não polares do óxido de zinco (ZnO), através da introdução de defeitos mecânicos por nanoindentação. A estrutura cristalina estável do ZnO é do tipo wurtzita, de forte caráter anisotrópico já observado em relação a propriedades como piezoeletricidade e polarização espontânea. O mecanismo de deformação mecânica desses sistemas ainda não está bem esclarecido e são de vital importância na otimização de dispositivos optoeletrônicos. A extensão dos defeitos para cada orientação do cristal foi analisada via microscopia eletrônica de transmissão e correlacionada com o movimento de planos basais {0001} de forma divergente, em faces não polares (1100) e (1120), e ao movimento de planos piramidais {1011} de forma convergente para faces polares (0001) e (0001). A extensão da deformação induzida abaixo da superfície foi avaliada, onde foi possível identificar a formação de discordâncias do tipo parafuso que se propagam através do sistema de escorregamento (1120)(0001), se propagando de forma altamente localizada abaixo da superfície. O início da deformação plástica em monocristais é marcado por eventos plásticos súbitos (pop-ins). Estes eventos foram identificados e analisados em função da força e da extensão da deformação gerada. A topografia e forma das impressões residuais foi analisada usando microscopia de força atômica. Os defeitos observados no plano superficial tenderam a se propagar em direções preferenciais num processo induzido pela formação de zonas de tensão em torno da indentação. A formação de zonas de tensão trativa em uma dada direção aumenta a mobilidade das discordâncias, enquanto zonas de tensão compressiva agem contribuindo para o travamento. Estas zonas foram identificadas e a magnitude desta tensão foi estimada via catodoluminescência. Observamos também que a face polar (0001) apresentou um comportamento reativo, onde defeitos localizados abaixo da superfície foram revelados através do processo de limpeza.
In this work, deformation mechanisms of polar and non-polar zinc oxide (ZnO) were studied by nanoindentation tests. The stable crystal structure of ZnO is the wurtzite with a strong anisotropic character observed in relation to the piezoelectricity and spontaneous polarization properties, for example. The mechanical deformation mechanisms of these sorts of materials are not yet fully understood, being of vital importance for optoelectronic devices optimization.For each ZnO crystallographic orientation, the induced defects damages were analyzed by transmission electron microscopy (TEM) and correlated with the slip of basal planes {0001} in the divergent directions for the both non-polar faces (1100) and (1120), as well as for the both polar faces (0001) and (0001). Screw perfect dislocations were identified by propagating through the slip system (1120)(0001). The beginning of plastic deformation in single crystals is marked by pop-ins events. Such events were identified and analyzed in function of the applied force and size. The residual impressions topography and shape were analyzed by atomic force microscopy (AFM). The observed defects on the surface were propagated in a preferred direction induced by stress components around the indentation. Tensile stress generation in a certain direction increases the dislocations mobility, while compressive stress contributes to pinning regions. Stress components were identified and their magnitudes were estimated by cathode luminescence method. The polar face (0001) showed a reactive behavior; some defects produced underneath the surface were revealed by samples cleaning process.
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Persson, Marcus. "Surfactants at non-polar surfaces." Doctoral thesis, KTH, Chemistry, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3444.

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The aim of this thesis work was to investigate theadsorption of surfactants to different nonpolar interfaces.Particularly, the effects of the polar group and the nature ofthe hydrophobic interface were elucidated. The interfacialbehavior of the liquid-vapor interface was investigated bymeans of surface tension measurements. Here the effect of thepolar group and the hydrocarbon chain length was investigatedin a systematic manner. It was found that the shorter of thetwo chains examined, decyl, generated a larger surface pressurecontribution than the longer, dodecyl. Furthermore, the sugarbased surfactants behaved differently as compared to theethylene oxide based ones. The former could be modelled byassuming a hard disc behavior of the head group while thelatter displayed polymeric behavior. The influence of saltconcentration on the surface tension behavior of an ionicsurfactant, sodium dodecyl sulphate, was investigated. Theresult could be rationalized by employing the Gouy- Chapmanmodel to the polar region. Furthermore, mixtures of two sugarbased surfactants were investigated by surface tensionmeasurements and the adsorbed amount of the two components atthe interface atdifferent concentrations and fractions in thebulk were obtained by applying the Gibbs surface tensionequation. It was found that the molecule with the smaller headgroup adsorbed preferentially, and more so as the totalsurfactant concentration was increased. These findings could beexplained by considering the interactions generated by thedifferent head groups. The adsorption of sugar surfactants toan isolated hydrophobic surface was studied by means of wettingmeasurements and the behavior was similar to that at theliquid-vapor interface. Wetting isotherms were measured on twodifferent hydrophobic surfaces where the covalently attachedhydrophobic layers were in a crystalline and fluid state,respectively. The wetting results revealed that the sugarsurfactants anchored in the fluid hydrophobic layer. This had asignificant influence on the force profile. For example, at thecrystalline surface the surfactant monolayers were easilyremoved as the surface came into contact at relatively lowapplied loads. This was not the case when the hydrophobic layerwas in a fluid state. Here a significant fraction of thesurfactants remained between the surfaces. Disjoining pressureisotherms were measured using a sugar based surfactant thatwere thoroughly purified and compared to the as receivedsample. Even the purified sample showed a double-layer forcealthough lower as compared to the as received, one. Asignificant difference in foam stability was also observed.

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Tabor, Richard F. "Surfactant kinetics in non-polar solvents." Thesis, University of Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508096.

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Chang, Tse Yang. "Characterisation of polar (0001) and non-polar (11-20) ultraviolet nitride semiconductors." Thesis, University of Cambridge, 2012. https://www.repository.cam.ac.uk/handle/1810/242371.

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UV and deep-UV emitters based on AlGaN/AlN heterostructures are very inefficient due to the high lattice mismatch of these films with sapphire substrates, leading to high dislocation densities. This thesis describes the characterisation of the nanostructures of a range of UV structures, including c-plane (polar) AlGaN epilayers grown on AlN template, and nonpolar GaN/AlGaN MQWs grown on a-plane GaN template. The results are based primarily on transmission electron microscopy (TEM), cathodoluminescence in the scanning electron microscope (SEM-CL), high-resolution X-ray diffraction (HRXRD) and atomic force microscopy (AFM) measurements. The structural and optical properties of various types of defect were examined in the c-plane AlGaN epilayers. Strain analysis based on in-situ wafer curvature measurements was employed to describe the strain relief mechanisms for different AlGaN compositions and to correlate the strain to each type of defect observed in the epilayers. This is followed by the investigation of AlN template growth optimisation, based on the TMA pre-dose on sapphire method to enhance the quality and the surface morphology of the template further. The initial growth conditions were shown to be critical for the final AlN film morphology. A higher TMA pre-dose has been shown to enable a better Al coverage leading to a fully coalesced AlN film at 1 μm thickness. An atomically smooth surface of the template was achieved over a large 10 x 10 μm AFM scale. Finally, the investigation of UV emitters based on nonpolar crystal orientations is presented. The SiNx interlayer was able to reduce the threading dislocation density but was also found to generate voids with longer SiNx growth time. The relationship between voids, threading dislocations, inversion domain boundaries and their associated V-defects and the variation in MQW growth rate has been discussed in detail.
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El-Agamey, Ali Abdel Ghani. "Acylperoxyl radicals and their reactions with carotenoids in polar and non-polar solvents." Thesis, Keele University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252583.

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Emery, Robert Michael. "Investigation into the growth of non-polar and semi-polar InGaN quantum dots." Thesis, University of Cambridge, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708911.

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Johnston, C. F. "Characterization of (11-20) non-polar and (11-22) semi-polar GaN epitaxial films." Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.605657.

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This thesis describes the microstructural characterization (using transmission electron microscopy [TEM], high resolution X-ray diffraction [HRXRD] and atomic force microscopy [AFM]) of non-polar (11-20) and semi-polar (11-22) GaN epitaxial layers. They were grown under a range of conditions on sapphire by metal-organic vapour phase epitaxy (MOVPE). The majority of the dislocations were partial dislocations bounding BSFs. As a consequence, defects were confined to the c-plane. A 3D-2D growth transition (where 3D islands are grown initially, then coalesced) reduced the defect density of non-polar GaN. Optimised coalescence conditions (i.e. a V/III ratio of 50) produced smooth films with a low RMS roughness. The effect of a 3D-2D growth transition on semi-polar material was less clear, but the microstructure was similar to non-polar GaN, in that the majority of dislocations were partials bounding BSFs. Since the growth conditions for the semi-polar epilayers were not optimised, surfaces were rough. Quantum wells grown on these templates were found to follow the surface roughness resulting in large fluctuations in quantum well width (of a few nanometres) and subsequent broadening of peaks in the photoluminescence spectra. To reduce the defect density, epitaxial laterial overgrowth (ELOG), SiNx interlayers and ScN interlayers were applied to non-polar and semi-polar films. ELOG was effective at reducing both BSF and dislocation density in both examples. Thick SiNx interlayers in non-polar GaN reduced dislocation density by a factor of 500 and BSF density by a factor of 5, compared to the template. An 8.5 nm ScN interlayer in semi-polar GaN reduced the dislocation density by a factor of 200 and BSF density by a factor of 14.
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Derry, Matthew J. "Polymerisation-induced self-assembly in non-polar solvents." Thesis, University of Sheffield, 2016. http://etheses.whiterose.ac.uk/13620/.

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This Thesis describes the reversible addition-fragmentation chain transfer (RAFT) dispersion polymerisation of benzyl methacrylate (BzMA) in non-polar solvents. Firstly, oil-soluble poly(lauryl methacrylate) (PLMA), poly(stearyl methacrylate) (PSMA) and poly(behenyl methacrylate) (PBhMA) macromolecular chain transfer agents (macro-CTAs) are synthesised via RAFT solution polymerisation in toluene. These macro-CTAs are then chain-extended in turn with varying amounts of BzMA in industrially-sourced mineral oil or a poly(α-olefin). Polymerisation-induced self-assembly (PISA) occurs under these conditions, where the soluble BzMA monomer polymerises to form an insoluble poly(benzyl methacrylate) (PBzMA) block, thus driving the in situ formation of spheres, worms or vesicles. Subtle differences in the phase diagrams constructed for PLMA-PBzMA diblock copolymer nano-objects are observed in different solvents. In such PISA formulations, the stabiliser block DP is an important parameter, because only kinetically-trapped spheres are accessible when sufficiently long stabilisers (e.g. PLMA39, PSMA18 or PBhMA37) are used. PLMA47-PBzMA100 spheres could be prepared at copolymer concentrations up to 50% w/w solids. Importantly, a highly convenient ‘one-pot’ synthetic protocol was developed, whereby 39 nm PLMA50-PBzMA100 spheres were prepared at 30% w/w solids within 9 h starting from LMA monomer. The phase diagram for PSMA13-PBzMAx diblock copolymer nanoparticles in mineral oil indicates that the final copolymer morphologies are only weakly dependent on copolymer concentration, which enables the synthesis of pure spheres, worms or vesicles at just 5.0% w/w solids. This facilitated in situ small-angle X-ray scattering (SAXS) studies during the PISA synthesis. When targeting PSMA31-PBzMA2000 spheres, the PBzMA core diameter and aggregation number per sphere (Ns) increased monotonically during the polymerisation. When targeting PSMA13-PBzMA150 vesicles, the full range of morphologies is observed, from soluble copolymer chains to the final vesicles via intermediate spheres and worms. Transmission electron microscopy (TEM) studies indicated that vesicles are formed from worms via transient octopi and jellyfish morphologies, which is consistent with observations previously reported for aqueous PISA formulations. A combination of dynamic light scattering (DLS), TEM and both in situ and post mortem SAXS analyses confirmed that the overall vesicle dimensions are conserved as the membrane thickens, which indicates an ‘inward growth’ mechanism. This is consistent with observations recently reported for an aqueous PISA formulation and hence suggests a universal vesicle growth mechanism for all PISA formulations. Dispersions of PSMA13-PBzMA65 worms form free-standing gels at 20 °C due to multiple inter-worm contacts, but heating leads to surface plasticisation. This induces a worm-to-sphere transition and concomitant degelation, since isotropic spheres cannot form inter-particle contacts at this copolymer concentration. The worm-to-sphere transition was characterised using TEM, DLS and rheology.
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Books on the topic "Non-polar"

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Louch, Jeff. Semipermeable membrane devices (SPMDs) for determining absolute or relative water column concentrations of non-polar chemicals in aqueous systems / by Jeff Louch. Research Triangle Park, N.C: National Council for Air and Stream Improvement, 2002.

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1960-, Geiger John, ed. Frozen in time: The fate of the Franklin expedition. Vancouver: Greystone Books, 1998.

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1960-, Geiger John, ed. Frozen in time: The fate of the Franklin expedition. Berkeley, Calif: Greystone Books, Douglas & McIntyre Pub. Group, 2004.

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John, Geiger, ed. Frozen in time: Fate of the Franklin expedition. London: Grafton, 1989.

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1960-, Geiger John, ed. Frozen in time: Unlocking the secrets of the Franklin expedition. New York: Dutton, 1988.

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Beattie, Owen. Frozen in time: The fate of the Franklin expedition. London: Bloomsbury, 1987.

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John, Geiger, ed. Frozen in time: The fate of the Franklin Expedition. London: Bloomsbury, 1993.

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Beattie, Owen. Frozen in time: Unlocking the secrets of the Franklin expedition. Saskatoon, Sask: Western Producer Prairie Books, 1988.

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1960-, Geiger John, ed. Frozen in time: Unlocking the secrets of the Franklin expedition. New York, N.Y., U.S.A: Plume, 1990.

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Polar Region (Living & Non-Living). Heinemann Library, 2007.

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Book chapters on the topic "Non-polar"

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de Leeuw, Simon W. "Polar / Non-Polar Fluid Mixtures." In Condensed Matter Theories, 485–98. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2934-7_42.

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Yakovlev, B. S., and L. V. Lukin. "Photoionization in Non-Polar Liquids." In Advances in Chemical Physics, 99–160. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470142844.ch3.

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Liska, Igor. "Non-Polar Micropollutants in Water Resources." In Security of Public Water Supplies, 161–70. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4241-0_13.

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Sakwe, Sakwe Aloysius, Yeon Suk Jang, and Peter J. Wellmann. "Defect Etching of Non-Polar and Semi-Polar Faces in SiC." In Materials Science Forum, 243–46. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-442-1.243.

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Walhout, P. K., J. C. Alfano, K. A. M. Thakur, and P. F. Barbara. "Vibrational Relaxation of I 2 − in Polar and Non-Polar Solvents." In Springer Series in Chemical Physics, 495–96. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85176-6_189.

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Shkapenko, Viktoriia, Vadim Kadoshnikov, and Irayida Pysanskaia. "Transformation of Non-polar Hydrocarbons in Soils." In Soil Science Working for a Living, 281–90. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-45417-7_28.

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Peper, Ferdinand, and Jia Lee. "On Non-polar Token-Pass Brownian Circuits." In Reversibility and Universality, 299–311. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-73216-9_14.

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Tsoneva, Yana, and Alia Tadjer. "Water Structuring at Non-Polar Fluid Interfaces." In Quantum Systems in Physics, Chemistry, and Biology, 119–38. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-50255-7_7.

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Dickerson, James H. "Electrophoretic Deposition of Nanocrystals in Non-polar Solvents." In Nanostructure Science and Technology, 131–55. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9730-2_3.

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Hansmann, U. H. E., and Y. Okamoto. "A Multicanonical Study of Non-Polar Amino Acids." In Springer Proceedings in Physics, 183–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-79293-9_17.

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Conference papers on the topic "Non-polar"

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Unlu, Hilmi, and Hadis Morkoc. "Effects Of Strains On The Polar/Non-Polar Heteroepitaxy." In 1988 Semiconductor Symposium, edited by Anupam Madhukar. SPIE, 1988. http://dx.doi.org/10.1117/12.947369.

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Padilla, A., J. Pérez, Marco Antonio Gigosos, and Manuel Ángel González. "The non Markovian Q-branch of polar diatomic molecules in non polar liquids." In SPECTRAL LINE SHAPES: Volume 15–19th International Conference on Spectral Line Shapes. AIP, 2008. http://dx.doi.org/10.1063/1.3026432.

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Hangleiter, Andreas, Torsten Langer, Philipp Henning, Fedor Alexej Ketzer, Philipp Horenburg, Ernst Ronald Korn, Heiko Bremers, and Uwe Rossow. "Radiative recombination in polar, non-polar, and semi-polar III-nitride quantum wells." In SPIE OPTO, edited by Jen-Inn Chyi, Hiroshi Fujioka, Hadis Morkoç, Yasushi Nanishi, Ulrich T. Schwarz, and Jong-In Shim. SPIE, 2017. http://dx.doi.org/10.1117/12.2252036.

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Wetzel, Christian, Mingwei Zhu, Yufeng Li, Wenting Hou, Liang Zhao, Wei Zhao, Shi You, et al. "Green LED development in polar and non-polar growth orientation." In SPIE Optical Engineering + Applications, edited by Ian T. Ferguson, Christoph Hoelen, Jianzhong Jiao, and Tsunemasa Taguchi. SPIE, 2009. http://dx.doi.org/10.1117/12.829513.

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Mikawa, Yutaka, Takayuki Ishinabe, Shinichiro Kawabata, Tae Mochizuki, Atsuhiko Kojima, Yuji Kagamitani, and Hideo Fujisawa. "Ammonothermal growth of polar and non-polar bulk GaN crystal." In SPIE OPTO, edited by Jen-Inn Chyi, Hiroshi Fujioka, and Hadis Morkoç. SPIE, 2015. http://dx.doi.org/10.1117/12.2078137.

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Chopra, Manish, Rohan Phatak, and N. Choudhury. "Transport of polar and non-polar solvents through a carbon nanotube." In SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4791161.

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Xu, Huangxia, Chaofan Chen, and Yanming Xue. "Short Polar-coded Non-coherent Receiver." In 2019 IEEE 3rd Information Technology, Networking, Electronic and Automation Control Conference (ITNEC). IEEE, 2019. http://dx.doi.org/10.1109/itnec.2019.8729533.

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Dai, Jincheng, Kai Niu, Zhongwei Si, and Jiaru Lin. "Polar coded non-orthogonal multiple access." In 2016 IEEE International Symposium on Information Theory (ISIT). IEEE, 2016. http://dx.doi.org/10.1109/isit.2016.7541447.

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Laib, Jonathan P., and Daniel M. Mittleman. "Terahertz absorption in non-polar, non-hydrogen-bonding liquids." In Conference on Lasers and Electro-Optics. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/cleo.2009.cmt4.

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Ye, Ming, and Hui Li. "A Performance Comparison of Systematic Polar Codes and Non-systematic Polar Codes." In 2018 International Conference on Mathematics, Modelling, Simulation and Algorithms (MMSA 2018). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/mmsa-18.2018.57.

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Reports on the topic "Non-polar"

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Paul Fini. High-Efficiency Non-Polar GaN-Based LEDs. Office of Scientific and Technical Information (OSTI), November 2010. http://dx.doi.org/10.2172/1001208.

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Gresser, Joseph D. Stable Biodegradable Polymers for Delivery of Both Polar and Non-Polar Drugs. Phase I. Fort Belvoir, VA: Defense Technical Information Center, October 1996. http://dx.doi.org/10.21236/adb222994.

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Ueda, Herbert T., and Pavel G. Talalay. Fifty Years of Soviet and Russian Drilling Activity in Polar and Non-Polar Ice: A Chronological History. Fort Belvoir, VA: Defense Technical Information Center, October 2007. http://dx.doi.org/10.21236/ada472548.

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Fini, P. Development of On-Demand Non-Polar and Semi-Polar Bulk Gallium Nitride Materials for Next Generation Electronic and Optoelectrode Devices. Fort Belvoir, VA: Defense Technical Information Center, March 2007. http://dx.doi.org/10.21236/ada464197.

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Sand, J. R. An analytical method of predicting Lee-Kesler-Ploecker binary interaction coefficients: Part 1, For non-polar hydrocarbon mixtures. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/105495.

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van Vark, Winnie, Ewoud Klopstra, and Joop Harmsen. Validation of ISO 16751 Soil Quality - Environmental availability of non-polar organic compounds : Determination of the potentially bioavailable fraction and the non-bioavailable fraction using a strong adsorbent or complexing agent. Wageningen: Wageningen Environmental Research, 2018. http://dx.doi.org/10.18174/465000.

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Andrieux, Charlotte. Touchez pas au grisbi! d’Albert Simonin : une initiation à l’argot et au monde interlope du «mitan» parisien dans le polar à la française, à l’usage des «non-affranchis» et des «gambergeologues avertis». Edicions de la Universitat de Lleida, 2018. http://dx.doi.org/10.21001/luc.21.22.12.

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