Thematische Bibliographien / Physics chemistry

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Auswahl der wissenschaftlichen Literatur zum Thema „Physics chemistry“

Autor: Grafiati

Veröffentlicht am 29. März 2025

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Zeitschriftenartikel zum Thema "Physics chemistry"

Hiebert, Erwin N. „Discipline Identification in Chemistry and Physics“. Science in Context 9, Nr. 2 (1996): 93–119. http://dx.doi.org/10.1017/s0269889700002362.

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The ArgumentDuring the nineteenth century, physicists and chemists, using different linguistic modes of expression, sought to describe the world for different purposes; thus, both disciplines gradually were nudged toward demarcation and self-image identification. In the course of doing so the rich complexity of the empire of chemistry was born. The essential challenge was closely connected with analysis, synthesis, and chemical process: learning the art of watching substances change and making substances change. Pursued in theory-poor and phenomenology-rich contexts chemistry nevertheless made itself intellectually, professionally, societally, and industrially creditable and attractive. The developing links between physics and chemistry are examined in this paper from the perspective of the discipline of chemistry more specifically than from the side of physics. Chemists came to believe that essentially physics was no more than mechanics. All else belonged to the domain of chemistry.Not before the last decades of the century were firm collaborative links and genuine reciprocity fostered between physics and chemistry, and then primarily on account of the common utility of scientific research tools. At a more fundamental level physics and chemistry, in contradistinction to all the other natural sciences, experienced partial overlap and convergence because of unique mutual reliance on the construction of systems each according to its own theoretical conceptions. Still amalgamation was unthinkable. Eventually physical chemistry was loosened from chemistry in the same way that, somewhat later, chemical physics was emancipated from physics. The intrinsic messiness of chemistry, one might suggest, tends more readily to foster Bohr's opinion that “there is no rock bottom to the study of nature,” rather than Einstein's view that “we can realistically, ultimately, put it all together.”

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Toibazarova, Altynkul, Nurbol Appazov, Zhanar Kuanysheva, Klara Darmagambet und Gulzhan Balykbayeva. „Experimental competence formation in chemistry teacher training“. Scientific Herald of Uzhhorod University Series Physics, Nr. 56 (12.03.2024): 1316–25. http://dx.doi.org/10.54919/physics/56.2024.131qo6.

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Relevance. The research relevance is determined by the need to adapt the educational system to the rapidly changing requirements of the labour market and technological progress. Purpose. The study aims to evaluate the effectiveness of analytical chemistry training programmes in leading universities of Kazakhstan from the point of view of developing the scientific competence of students necessary for employment. Methodology. The study employs comparative, qualitative, and statistical analyses, questionnaires, surveys and observation. Results. The study examines the role of universities in training analytical specialists. The requirements of the labour market and academic institutions for candidates for positions in analytical chemistry, as well as the current state of research and development in training, were considered. The findings showed that many university graduates trained in analytical chemistry prefer not to go to work in industry or factory laboratories, but plan to stay in academia and continue their research. This indicates the need to revise curricula to better meet the requirements of the labour market and academic institutions. Problems and gaps in current programmes and methods of teaching analytical chemistry at universities in Kazakhstan have been identified. Approaches to strengthening the practical component of courses have been critically analysed, considering the current requirements and assessments of industry specialists. Conclusions. The study highlighted the high demand for qualified specialists, emphasizing that the issue lies not in the shortage of vacancies but in the level of training. The practical significance of the study lies in the fact that its results can be used to modernise the system of education in the field of analytical chemistry and improve curricula and teaching methods. This, in turn, will help to improve the quality of training of analytical chemists who will be able to meet the needs of the labour market and scientific institutions. Keywords: active learning; analysis methodology; students; specialist qualifications; researchers

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Bolton, Christ A. „Physics before chemistry“. Physics Teacher 25, Nr. 9 (Dezember 1987): 545. http://dx.doi.org/10.1119/1.2342368.

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Gavroglu, Kostas. „Is chemistry physics?“ Nature 369, Nr. 6480 (Juni 1994): 452. http://dx.doi.org/10.1038/369452a0.

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Khazanov, G. V. „Ionospheres: Physics, plasma physics, and chemistry“. Eos, Transactions American Geophysical Union 82, Nr. 46 (2001): 556. http://dx.doi.org/10.1029/01eo00328.

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Ganguli, Supriya B. „Ionospheres physics, plasma physics and chemistry“. Journal of Atmospheric and Solar-Terrestrial Physics 65, Nr. 6 (April 2003): 779. http://dx.doi.org/10.1016/s1364-6826(03)00002-6.

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Whittingham, M. Stanley. „Materials in the Undergraduate Chemistry Curriculum“. MRS Bulletin 15, Nr. 8 (August 1990): 40–45. http://dx.doi.org/10.1557/s0883769400058942.

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Although solids are one of the three states of matter, and the solid state is pervasive throughout science and our lives, students would not know it from the standard chemistry curriculum, which still emphasizes small molecules. Despite this education, a significant proportion (more than 30%) of all chemists end up as practitioners of materials chemistry, either in inorganic solids or in polymers, and they must therefore obtain on-the-job education. Not only should this need be reflected in the curriculum, but it should be possible through modern areas of chemistry such as materials to bring some of the excitement of the practicing chemist to the undergraduate student's first chemistry course, perhaps turning around the flight from science, and from chemistry and physics in particular. The American Chemical Society is encouraging this approach through the proposal of a certified BS degree in chemistry with emphasis in materials. To place the present position in perspective, one only needs to look at the recent figures tabulated by the National Science Foundation; there is a tremendous attrition of students planning to major in science and engineering during the freshman year (See Table I).Potential science majors are indeed there, but they are being lost due to their first experiences, which are usually in general chemistry and calculus, and a lesser number in biology and physics. It is therefore imperative that these courses encourage students rather than kill their enthusiasm.

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Raman, K. V. „Some Features of Java Language Illustrated through Examples from Chemistry“. Mapana - Journal of Sciences 1, Nr. 2 (03.07.2003): 22–56. http://dx.doi.org/10.12723/mjs.2.5.

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Computer programming has been used effectively by theoretical chemists and organic chemists to solve various types of problem in chemistry. Initially the languages used for computations in chemistry were FORTRAN and BASIC. Later the Pascal language was used for solving problems in chemistry and physics. Recently the languages C and C++ and Java have been used to solve problems in chemistry. In this paper I will illustrate features of C, C++ choosing examples from chemistry. Computer programming has been used effectively by theoretical chemists and organic chemists to solve various types of problem in chemistry. Initially the languages used for computations in chemistry were FORTRAN and BASIC. Later the Pascal language was used for solving problems in chemistry and physics. Recently the languages C and C++ and Java have been used to solve problems in chemistry. In this paper I will illustrate features of C, C++ choosing examples from chemistry. Some examples presented in this these languages are Program to calculate reduced mass of homo diatomic or hetero diatomic Program to calculate the molecular weight of a tetra atomic system ABCD Program to calculate NMR frequencies of spin 1/2 nuclei only Program to calculate NMR and ESR frequencies The examples presented in Java 2 are Program to calculate unit cell dimension of a crystal Program to generate the chair form and boat form of cyclohexane. The examples presented in this monograph will help researchers in theoretical chemistry and organic chemistry to develop their own software.

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Mysen, Bjorn. „Physics and chemistry of silicate glasses and melts“. European Journal of Mineralogy 15, Nr. 5 (17.11.2003): 781–802. http://dx.doi.org/10.1127/0935-1221/2003/0015-0781.

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BAUM, RUDY M. „No Chemistry, No Physics“. Chemical & Engineering News 79, Nr. 36 (03.09.2001): 5. http://dx.doi.org/10.1021/cen-v079n036.p005.

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Dissertationen zum Thema "Physics chemistry"

Sanders, Jacob N. „Compressed Sensing for Chemistry“. Thesis, Harvard University, 2016. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493432.

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Many chemical applications, from spectroscopy to quantum chemistry, involve measuring or computing a large amount of data, and then compressing this data to retain the most chemically-relevant information. In contrast, compressed sensing is an emergent technique that makes it possible to measure or compute an amount of data that is roughly proportional to its information content. In particular, compressed sensing enables the recovery of a sparse quantity of information from significantly undersampled data by solving an l1-optimization problem. This thesis represents the application of compressed sensing to problems in chemistry. The first half of this thesis is about spectroscopy. Compressed sensing is used to accelerate the computation of vibrational and electronic spectra from real-time time-dependent density functional theory simulations. Using compressed sensing as a drop-in replacement for the discrete Fourier transform, well-resolved frequency spectra are obtained at one-fifth the typical simulation time and computational cost. The technique is generalized to multiple dimensions and applied to two-dimensional absorption spectroscopy using experimental data collected on atomic rubidium vapor. Finally, a related technique known as super-resolution is applied to open quantum systems to obtain realistic models of a protein environment, in the form of atomistic spectral densities, at lower computational cost. The second half of this thesis deals with matrices in quantum chemistry. It presents a new use of compressed sensing for more efficient matrix recovery whenever the calculation of individual matrix elements is the computational bottleneck. The technique is applied to the computation of the second-derivative Hessian matrices in electronic structure calculations to obtain the vibrational modes and frequencies of molecules. When applied to anthracene, this technique results in a threefold speed-up, with greater speed-ups possible for larger molecules. The implementation of the method in the Q-Chem commercial software package is described. Moreover, the method provides a general framework for bootstrapping cheap low-accuracy calculations in order to reduce the required number of expensive high-accuracy calculations.
Chemical Physics

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McClean, Jarrod Ryan. „Algorithms Bridging Quantum Computation and Chemistry“. Thesis, Harvard University, 2015. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467376.

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The design of new materials and chemicals derived entirely from computation has long been a goal of computational chemistry, and the governing equation whose solution would permit this dream is known. Unfortunately, the exact solution to this equation has been far too expensive and clever approximations fail in critical situations. Quantum computers offer a novel solution to this problem. In this work, we develop not only new algorithms to use quantum computers to study hard problems in chemistry, but also explore how such algorithms can help us to better understand and improve our traditional approaches. In particular, we first introduce a new method, the variational quantum eigensolver, which is designed to maximally utilize the quantum resources available in a device to solve chemical problems. We apply this method in a real quantum photonic device in the lab to study the dissociation of the helium hydride (HeH$^{+}$) molecule. We also enhance this methodology with architecture specific optimizations on ion trap computers and show how linear-scaling techniques from traditional quantum chemistry can be used to improve the outlook of similar algorithms on quantum computers. We then show how studying quantum algorithms such as these can be used to understand and enhance the development of classical algorithms. In particular we use a tool from adiabatic quantum computation, Feynman's Clock, to develop a new discrete time variational principle and further establish a connection between real-time quantum dynamics and ground state eigenvalue problems. We use these tools to develop two novel parallel-in-time quantum algorithms that outperform competitive algorithms as well as offer new insights into the connection between the fermion sign problem of ground states and the dynamical sign problem of quantum dynamics. Finally we use insights gained in the study of quantum circuits to explore a general notion of sparsity in many-body quantum systems. In particular we use developments from the field of compressed sensing to find compact representations of ground states. As an application we study electronic systems and find solutions dramatically more compact than traditional configuration interaction expansions, offering hope to extend this methodology to challenging systems in chemical and material design.
Chemical Physics

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Das, Ujjal. „Electronic structure studies of semiconductor surface chemistry and aluminum oxide cluster chemistry“. [Bloomington, Ind.] : Indiana University, 2008. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3344570.

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Thesis (Ph. D.)--Indiana University, Dept. of Chemistry, 2008.
Title from PDF t.p. (viewed Oct. 7, 2009). Source: Dissertation Abstracts International, Volume: 70-02, Section: B, page: 1054. Adviser: Krishnan Raghavachari.

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Domke, Andreas. „Chemistry and physics of diamond surfaces“. Thesis, University of Liverpool, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367131.

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This thesis is concerned with the chemistry and physics of C(100) surfaces of diamond. The polished and cleaned C(100) surface is examined by surface microscopy (Atomic-force Microscopy), electron diffraction (Low-energy Electron Diffraction) and photoemission (X-ray Photoelectron Spectroscopy and Ultra-violet Photoelectron Spectroscopy). Results are presented on the presence of oxygen, nitrogen and hydrogen/deuterium on the C(100) surface. Finally, the valence band structure of diamond is probed by angle-resolved photoemission. We have confirmed by AFM that the grooves from the soft polishing process are present on a polished C(100) surface and found sporadic traces of hard polish on a surface polished in the soft polishing direction. XPS studies have verified heating cycles by electron beam bombardment as a suitable cleaning procedure for pure reconstructed C(100) surfaces. By allowing the crystal to cool slowly, the first experimental evidence of quarter-order LEED spots have been found, which suggest that buckled dimerisation might have occurred similar to those on Si(100) and Ge(100). We present the first experimental electron spectroscopy results for a nitrogen impurity in diamond by showing the N KLL Auger spectrum. An attempt to smooth a C(100) surface of diamond by an atomic hydrogen plasma did not succeed. AFM studies showed no evidence for the surface smoothing reported in other studies, but the results enable us to explain the different plasma published in the literature. The valence band of diamond is investigated by off-normal ARUPS. The features observed are consistent with possible transitions, which are determined using bulk band structure calculations and comparison with the experimental binding energies.

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Babbush, Ryan Joseph. „Towards Viable Quantum Computation for Chemistry“. Thesis, Harvard University, 2015. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467325.

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Since its introduction one decade ago, the quantum algorithm for chemistry has been among the most anticipated applications of quantum computers. However, as the age of industrial quantum technology dawns, so has the realization that even “polynomial” resource overheads are often prohibitive. There remains a large gap between the capabilities of existing hardware and the resources required to quantum compute classically intractable problems in chemistry. The primary contribution of this dissertation is to take meaningful steps towards reducing the costs of three approaches to quantum computing chemistry. First, we discuss how chemistry problems can be embedded in Hamiltonians suitable for commercially manufactured quantum annealing machines. We introduce schemes for more efficiently compiling problems to annealing Hamiltonians and apply the techniques to problems in protein folding, gene expression, and cheminformatics. Second, we introduce the first adiabatic quantum algorithm for fermionic simulation. Towards this end, we develop tools which embed arbitrary universal Hamiltonians in constrained hardware at a reduced cost. Finally, we turn our attention to the digital quantum algorithm for chemistry. By exploiting the locality of physical interactions, we quadratically reduce the number of terms which must be simulated. By analyzing the scaling of time discretization errors in terms of chemical properties, we obtain significantly tighter bounds on the minimum number of time steps which must be simulated. Also included in this dissertation is a protocol for preparing configuration interaction states that is asymptotically superior to all prior results and the details of the most accurate experimental quantum simulation of chemistry ever performed.
Chemical Physics

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Tilling, Ian. „Physics and chemistry of gas in discs“. Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/8271.

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Protoplanetary discs set the initial conditions for planet formation. By combining observations with detailed modelling, it is possible to constrain the physics and chemistry in such discs. I have used the detailed thermo-chemical disc model ProDiMo to explore the characteristics of the gas in protoplanetary discs, particularly in Herbig Ae objects. I have assessed the ability of various observational data to trace the disc properties. This has involved a number of different approaches. Firstly I compute a series of disc models with increasing mass, in order to test the diagnostic powers of various emission lines, in particular as gas mass tracers. This approach is then expanded to a large multiparameter grid of ~ 10 5 disc models. I have helped to develop a tool for analysing and plotting the huge quantity of data presented by such a model grid. Following this approach I move on to a detailed study of the Herbig Ae star HD 163296, attempting to fit the large wealth of available observations simultaneously. These include new Herschel observations of the far-infrared emission lines, as well as interferometric CO observations and a large number of continuum data. This study addresses the topical issues of the disc gas/dust ratio, and the treatment of the disc outer edge. It explores the effects of dust settling, UV variability and stellar X-ray emission on the disc chemistry and line emission. There is possible evidence for gas-depletion in the disc of HD 163296, with the line emission enhanced by dust settling, which would indicate a later evolutionary stage for this disc than suggested by other studies. Finally, I work to improve the treatment of the gas heating/cooling balance in ProDiMo, by introducing a non-LTE treatment of the atomic hydrogen line transitions and bound-free continuum transitions. I explore the effects of this on the disc chemical and thermal structure, and assess its impact in terms of the observable quantities.

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Michalak, David Jason Gray Harry B. „Physics and chemistry of silicon surface passivation /“. Diss., Pasadena, Calif. : Caltech, 2006. http://resolver.caltech.edu/CaltechETD:etd-05082006-074414.

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Marelli, Elena. „New chemistry and physics from transition-metal cyanides“. Thesis, University of Reading, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627647.

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Thompson, Travis W. „Tuning the Photochemical Reactivity of Electrocyclic Reactions| A Non-adiabatic Molecular Dynamics Study“. Thesis, California State University, Long Beach, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10839950.

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We use non-adiabatic ab initio molecular dynamics to study the influence of substituent side groups on the photoactive unit (Z)-hexa-1,3,5-triene (HT). The Time-Dependent Density Functional Theory Surface Hopping method (TDDFT-SH) is used to investigate the influence of substituted isopropyl and methyl groups on the excited state dynamics. The 1,4 and 2,5-substituted molecules are simulated: 2,5-dimethylhexa-1,3,5-triene (DMHT), 2-isopropyl-5-methyl-1,3,5-hexatriene (2,5-IMHT), 3,7-dimethylocta-1,3,5-triene (1,4-IMHT), and 2,5-diisopropyl-1,3,5-hexatriene (DIHT). We find that HT and 1,4-IMHT have the lowest ring-closing branching ratios of 5.3% and 1.0%, respectively. For the 2,5-substituted derivatives, the branching ratio increases with increasing size of the substituents, exhibiting yields of 9.78%, 19%, and 24% for DMHT, 2,5-IMHT, and DIHT, respectively. The reaction channels are shown to prefer certain conformation configurations at excitation, where the ring-closing reaction tends to originate from the gauche-Z-gauche (gZg) rotamer almost exclusively. In addition, there is a conformational dependency on absorption, gZg conformers have on average lower S₁ ← S₀ excitation energies that the other rotamers. Furthermore, we develop a method to calculate a predicted quantum yield that is in agreement with the wavelength-dependence observed in experiment for DMHT. In addition, the quantum yield method also predicts DIHT to have the highest CHD yield of 0.176 at 254 nm and 0.390 at 290 nm.

Additionally, we study the vitamin D derivative Tachysterol (Tachy) which exhibits similar photochemical properties as HT and its derivatives. We find the reaction channels of Tachy also have a conformation dependency, where the reactive products toxisterol-D1 (2.3%), previtamin D (1.4%) and cyclobutene toxisterol (0.7%) prefer cEc, cEt, and tEc configurations at excitation, leaving the tEt completely non-reactive. The rotamers similarly have a dependence on absorption as well, where the cEc configuration has the lowest energy S₁ ← S₀ excitation of the rotamers. The wavelength dependence of the rotamers should lead to selective properties of these molecules at excitation. An excitation to the red-shifted side of the maximum absorption peak will on average lead to excitations of the gZg rotamers more exclusively.

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Trabajo, Pedro Garcia. „The chemistry and physics of stabiliser additives in polyolefins“. Thesis, University of Sussex, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318606.

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Bücher zum Thema "Physics chemistry"

Royal Society of Chemistry (Great Britain). Physical chemistry chemical physics: PCCP. Cambridge, England: Royal Society of Chemistry, 1999.

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Pearce, Eli M., und G. E. Zaikov. New steps in physical chemistry, chemical physics, and biochemical physics. Herausgegeben von Kirshenbaum Gerald S. Hauppauge, N.Y: Nova Science Publishers, 2012.

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Schunk, R. W. Ionospheres: Physics, plasma physics, and chemistry. 2. Aufl. Cambridge, UK: Cambridge University Press, 2009.

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Andrew, Nagy, Hrsg. Ionospheres: Physics, plasma physics, and chemistry. Cambridge, UK: Cambridge University Press, 2009.

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Pople, Stephen. Physics. 2. Aufl. Oxford: Oxford University Press, 1996.

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(Firm), Knovel, Hrsg. Encyclopedia of chemical physics and physical chemistry. Bristol, UK: Institute of Physics Publishing, 2001.

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Pignatello, Rosario. Biomaterials: Physics and chemistry. Rijeka, Croatia: InTech, 2011.

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Prassides, Kosmas. Physics and Chemistry of the Fullerenes. Dordrecht: Springer Netherlands, 1994.

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Battaglia, Franco. Fundamentals in Chemical Physics. Dordrecht: Springer Netherlands, 1998.

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Battaglia, Franco. Fundamentals in chemical physics. Dordrecht: Kluwer Academic, 1998.

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Buchteile zum Thema "Physics chemistry"

Liberman, Michael A. „Combustion Chemistry“. In Combustion Physics, 1–32. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-85139-2_1.

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Hall, George M. „Physics and Chemistry“. In The Ingenious Mind of Nature, 185–203. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-6020-7_10.

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Simões, Ana. „Quantum Chemistry“. In Compendium of Quantum Physics, 518–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-70626-7_158.

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Battaglia, Franco, und Thomas F. George. „Quantum Chemistry“. In Fundamentals in Chemical Physics, 141–82. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-1636-9_4.

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Jortner, Joshua, und R. D. Levine. „Photoselective Chemistry“. In Advances in Chemical Physics, 1–114. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470142677.ch1.

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Nicolet, Marcel. „Atmospheric Chemistry“. In Advances in Chemical Physics, 63–78. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470142790.ch5.

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Biederman, H., und Y. Osada. „Plasma chemistry of polymers“. In Polymer Physics, 57–109. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/3-540-52159-3_6.

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Bentley, J., und G. P. A. Turner. „Colour physics and chemistry“. In Introduction to Paint Chemistry and principles of paint technology, 77–88. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-3180-1_6.

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Chapple, J. A. V. „Astronomy, Physics, Chemistry, Meteorology“. In Science and Literature in the Nineteenth Century, 20–57. London: Macmillan Education UK, 1986. http://dx.doi.org/10.1007/978-1-349-18470-5_2.

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Kilgour, O. F. G. „Food, Physics and Chemistry“. In Mastering Nutrition, 16–34. London: Macmillan Education UK, 1985. http://dx.doi.org/10.1007/978-1-349-17814-8_2.

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Konferenzberichte zum Thema "Physics chemistry"

Duley, W. W. „Physics, chemistry and microwelding“. In ICALEO® 2002: 21st International Congress on Laser Materials Processing and Laser Microfabrication. Laser Institute of America, 2002. http://dx.doi.org/10.2351/1.5065735.

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Kawai, Maki, Yousoo Kim, Beverly Karplus Hartline, Renee K. Horton und Catherine M. Kaicher. „Single-Molecule Chemistry“. In WOMEN IN PHYSICS: Third IUPAP International Conference on Women in Physics. AIP, 2009. http://dx.doi.org/10.1063/1.3137907.

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KLEMPERER, WILLIAM. „SOME THOUGHTS ON INTERSTELLAR CHEMISTRY“. In Contributions to Atomic, Molecular, and Optical Physics, Astrophysics, and Atmospheric Physics. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 2009. http://dx.doi.org/10.1142/9781848164703_0006.

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Haba, Hiromitsu, Daiya Kaji, Yoshitaka Kasamatsu, Hidetoshi Kikunaga, Yukiko Komori, Yuki Kudou, Kouji Morimoto et al. „Superheavy Element Nuclear Chemistry at RIKEN“. In NUCLEAR PHYSICS TRENDS: 7th Japan-China Joint Nuclear Physics Symposium. AIP, 2010. http://dx.doi.org/10.1063/1.3442621.

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THADDEUS, PATRICK. „STILL MORE THOUGHTS ON INTERSTELLAR CHEMISTRY“. In Contributions to Atomic, Molecular, and Optical Physics, Astrophysics, and Atmospheric Physics. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 2009. http://dx.doi.org/10.1142/9781848164703_0011.

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Kuzmany, Hans, Jörg Fink, Michael Mehring und Siegmar Roth. „PHYSICS AND CHEMISTRY OF FULLERENES AND DERIVATIVES“. In International Winterschool on Electronic Properties of Novel Materials. WORLD SCIENTIFIC, 1995. http://dx.doi.org/10.1142/9789814532327.

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Rosa, Lorenzo, Kai Sun, Ewa Kowalska und Saulius Juodkazis. „Novel plasmonic applications in physics and chemistry“. In 2011 International Quantum Electronics Conference (IQEC) and Conference on Lasers and Electro-Optics (CLEO) Pacific Rim. IEEE, 2011. http://dx.doi.org/10.1109/iqec-cleo.2011.6194053.

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Naskrecki, Ryszard, Carlos Granja, Claude Leroy und Ivan Stekl. „Ultrashort Laser Pulses in Physics and Chemistry“. In Nuclear Physics Medthods and Accelerators in Biology and Medicine. AIP, 2007. http://dx.doi.org/10.1063/1.2825781.

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Iyer, M. S. Karthikeyan, und Ajay V. Singh. „Detonation chemistry of jet A“. In APPLIED PHYSICS OF CONDENSED MATTER (APCOM 2022). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0127727.

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Dakasheva, Tanzila Mukhtarovna. „L.Y. KARPOV RESEARCH INSTITUTE OF PHYSICS AND CHEMISTRY: THE «EXCHANGE ZONE» BETWEEN CHEMISTRY AND PHYSICS (THE 1950S AND 1960S)“. In Российская наука: актуальные исследования и разработки. Самара: Самарский государственный экономический университет, 2022. http://dx.doi.org/10.46554/russian.science-2022.02-1-71/75.

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Berichte der Organisationen zum Thema "Physics chemistry"

Onishi, Y., H. C. Reid und D. S. Trent. Dilution physics modeling: Dissolution/precipitation chemistry. Office of Scientific and Technical Information (OSTI), September 1995. http://dx.doi.org/10.2172/109665.

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Va'vra, Jaroslav. Physics and Chemistry of Aging - Early Developments. Office of Scientific and Technical Information (OSTI), Februar 2002. http://dx.doi.org/10.2172/798985.

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Greenbaum, E. (The physics and chemistry of microalgal photosynthesis). Office of Scientific and Technical Information (OSTI), September 1989. http://dx.doi.org/10.2172/5622196.

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Hellwig, Helmut. Physics, chemistry and engineering in the 1990's. Gaithersburg, MD: National Institute of Standards and Technology, 1990. http://dx.doi.org/10.6028/nist.ir.90-4284.

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Klots, C. E. (Physics and chemistry of van der Waals particles). Office of Scientific and Technical Information (OSTI), Oktober 1990. http://dx.doi.org/10.2172/6608231.

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Jackson, Koblar A. The Physics and Chemistry of Cluster-based Catalyst Systems. Office of Scientific and Technical Information (OSTI), November 2018. http://dx.doi.org/10.2172/1481255.

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Buchanan, Christopher C. A Computational Examination of Detonation Physics and Blast Chemistry. Fort Belvoir, VA: Defense Technical Information Center, August 2011. http://dx.doi.org/10.21236/ada548571.

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Ruzsinsky, Adrienn. Exploring the Random Phase Approximately for materials chemistry and physics. Office of Scientific and Technical Information (OSTI), März 2015. http://dx.doi.org/10.2172/1183045.

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Goddard III, William A., Michael Ortiz und Sergey Zybin. The Fundamental Chemistry and Physics of Munitions under Extreme Conditions. Fort Belvoir, VA: Defense Technical Information Center, Februar 2011. http://dx.doi.org/10.21236/ada544994.

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