Relevant bibliographies by topics / Physical Chemistry

Contents

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

Academic literature on the topic 'Physical Chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 December 2024

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Journal articles on the topic "Physical Chemistry"

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de Berg, Kevin Charles. "The significance of the origin of physical chemistry for physical chemistry education: the case of electrolyte solution chemistry." Chem. Educ. Res. Pract. 15, no. 3 (2014): 266–75. http://dx.doi.org/10.1039/c4rp00010b.

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Physical Chemistry's birth was fraught with controversy, a controversy about electrolyte solution chemistry which has much to say about how scientific knowledge originates, matures, and responds to challenges. This has direct implications for the way our students are educated in physical chemistry in particular and science in general. The incursion of physical measurement and mathematics into a discipline which had been largely defined within a laboratory of smells, bangs, and colours was equivalent to the admission into chemistry of the worship of false gods according to one chemist. The controversy can be classified as a battle betweendissociationistson the one hand andassociationistson the other; between theEuropeanson the one hand and theBritishon the other; between theionistson the one hand and thehydrationistson the other. Such strong contrasts set the ideal atmosphere for the development of argumentation skills. The fact that a compromise position, first elaborated in the late 19th century, has recently enhanced the explanatory capacity for electrolyte solution chemistry is challenging but one in which students can participate to their benefit.
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Isbell, Terry A. "Chemistry and physical properties of estolides." Grasas y Aceites 62, no. 1 (February 16, 2011): 8–20. http://dx.doi.org/10.3989/gya/010810.

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Galwey, Andrew K. "Physical chemistry." Endeavour 17, no. 1 (March 1993): 44. http://dx.doi.org/10.1016/0160-9327(93)90029-3.

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Boddenberg, B. "Physical Chemistry." Zeitschrift für Physikalische Chemie 212, Part_1 (January 1999): 113–14. http://dx.doi.org/10.1524/zpch.1999.212.part_1.113.

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Bhattacharyya, Kankan, Gang-yu Liu, and Martin T. Zanni. "“New Physical Chemistry Insight” in Experimental Bio-Physical Chemistry." Journal of Physical Chemistry B 121, no. 27 (July 13, 2017): 6455. http://dx.doi.org/10.1021/acs.jpcb.7b05757.

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Krenos, John. "Physical Chemistry: Thermodynamics (Horia Metiu); Physical Chemistry: Statistical Mechanics (Horia Metiu); Physical Chemistry: Kinetics (Horia Metiu); Physical Chemistry: Quantum Mechanics (Horia Metiu)." Journal of Chemical Education 85, no. 2 (February 2008): 206. http://dx.doi.org/10.1021/ed085p206.

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Williams, Ian H. "Physical Organic Chemistry in the 21st Century: A Q1 Progress Report." Chemistry International 44, no. 2 (April 1, 2022): 10–13. http://dx.doi.org/10.1515/ci-2022-0203.

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Abstract In 1997, a collection of twenty personal perspectives from eminent chemists was published in Pure and Applied Chemistry to mark the centenary of physical organic chemistry [1]. This Symposium in Print, entitled Physical Organic Chemistry in the 21st Century (POC21C), was organized by the IUPAC Commission on Physical Organic Chemistry, which was chaired at that time by Tom Tidwell, who contributed a historical prologue in which he suggested Stieglitz’s 1899 proposal of carbocations as reaction intermediates as (unwittingly) having given birth to the discipline. The principal authors were Edward Arnett, Daniel Bellus, Ron Breslow, Fulvio Cacace, Jan Engberts, Marye Anne Fox, Ken Houk, Keith Ingold, Alan Katritzky, Ed Kosower, Meir Lahav, Teruaki Mukaiyama, Oleg Nefedov, George Olah, John Roberts, Jean-Michel Savéant, Helmut Schwarz, Andrew Streitwieser, Frank Westheimer, and Akio Yamamoto. Tidwell noted that, whereas they were not all known as physical organic chemists, yet they had all used the tools of this discipline in their work and were able to comment upon the utility of physical organic chemistry for the practice of other areas of chemistry as well. The theme that ran through all the essays was that the future of the field lay in an interdisciplinary approach, that physical organic chemists would use all the tools available to them, and that they would not be fettered to narrow views.
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WU, Kai. "Surface Physical Chemistry." Acta Physico-Chimica Sinica 34, no. 12 (2018): 1299–301. http://dx.doi.org/10.3866/pku.whxb201804192.

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Raven, J. A., C. Rossi, and E. Tiezzi. "Ecological Physical Chemistry." Journal of Applied Ecology 31, no. 1 (February 1994): 193. http://dx.doi.org/10.2307/2404611.

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Murphy, John A. "Physical organic chemistry." Beilstein Journal of Organic Chemistry 6 (November 3, 2010): 1025. http://dx.doi.org/10.3762/bjoc.6.116.

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Dissertations / Theses on the topic "Physical Chemistry"

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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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Ngabe, Barnabe. "Physical chemistry of sulphide self-heating." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123024.

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ABSTRACTA prerequisite step towards building a self-heating (SH) model for sulphide materials is the determination of physico-chemical parameters such as the specific heat capacity (Cp), and the energy of activation (Ea). The specific heat capacity of one copper and three nickel concentrates was determined over the temperature range 50 to 80oC in the presence of 6% moisture using the self-heating (SH) apparatus and confirmed by Drop Calorimetry. The Cp values from both techniques were comparable. The Cp values were similar for all concentrates increasing from 0.4 to 1.4 Jg-1K-1 as temperature increased from 50 to 80oC. From the Cp values, the enthalpy change (ΔH), the entropy change (ΔS) and the Gibbs free energy change (ΔG) for self-heating, were determined. The ΔG was negative, demonstrating that self-heating of the concentrates was spontaneous.Using the self-heating apparatus the, activation energy (Ea) was determined for the Ni-and Cu-concentrates and for pairs of sulphide minerals. The Ea ranged from 22 to 30 kJ.mol-1, implying a common reaction. Further support for a common reaction is the strong positive correlation between Ea and ln(QA/Cp) where Q (J.kg-1) is the heat of reaction causing self-heating and A the Arrhenius pre-exponential factor (s-1). Comparing to literature, the Ea values correspond to partial oxidation of hydrogen sulphide, supporting the contention that H2S may be an intermediate product in the self-heating of sulphide minerals. A positive relationship between Ea and the rest potential difference (ΔV) for the sulphide pairs and a negative relationship between Cp and ΔV were demonstrated which support a connection between self-heating and the galvanic effect.
RESUMÉLa réalisation d'un modèle mathématique de l'auto-échauffement des concentrés sulfurés de nickel et de cuivre et des mélanges des minerais sulfurés, enjoint à la détermination des paramètres physico-chimiques tels que les capacités de chaleur spécifiques (Cp), et les énergies d'activation (Ea). Les capacités de chaleur spécifiques d'un concentré de cuivre et de trois concentrés de nickel contenant 6% d'humidité, ont été déterminées par utilisation d'un instrument de mesure de vitesse d'auto – échauffement et validées par la calorimétrie de chute dans l'intervalle de températures allant de 50 à 80oC. Les Cp (0.4 à 1.4 Jg-1K-1) obtenues sont similaires pour tous les échantillons. A partir des valeurs des Cp, les variations de l'enthalpie (ΔH), l'entropie (ΔS) et de l'énergie libre de Gibbs (ΔG) de l'auto échauffement ont été déterminées. La valeur négative de ΔG confirme le caractère spontané de l'auto échauffement des minerais sulfurés.Les énergies d'activation (Ea) pour l'auto-échauffement des concentrés de nickel et cuivre et des paires de minerais sulfurés étaient déterminées en faisant usage de l'appareil d'auto-échauffement. Les Ea ainsi obtenues oscillent entre 22 et 30 kJ.mol-1 : Ce qui est suggestif d'une rèaction chimique commune gouvernant l'auto-échauffement de ces matériaux. Ce fait est corroboré par la forte corrélation obtenue entre Ea et ln(QA/Cp) (Q (J.kg-1) est la chaleur de la rèaction chimique responsable de l'auto-échauffement et A (s-1) la constante d'Arrhenius).Ensuite celles-ci sont similaires à celle de l'oxydation partielle du H2S. Il se pourrait, ce faisant, que H2S soit un composé intermediaire lors de l'auto–échauffement des sulfures.Enfin, la corrélation positive entre Ea et la difference de potential (ΔV) dans les paires de minerais sulfurés et celle negative entre Cp et ΔV sont une preuve qu'il existe bel et bien une connection entre l'auto-échauffement et l'effet galvanique.
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Christy, R. K. "The physical chemistry of drug formulations." Thesis, University of Kent, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362185.

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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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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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Grimes-Marchan, Thomas V. Cundari Thomas R. "Quantum perspectives on physical and inorganic chemistry." [Denton, Tex.] : University of North Texas, 2007. http://digital.library.unt.edu/permalink/meta-dc-5172.

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Portal, Christophe. "Approaches to high throughput physical organic chemistry." Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/2434.

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Over the past ten years, the development of High Throughput (HT) synthetic chemistry techniques has allowed the rapid preparation of libraries of hundreds to thousands of compounds. These tools are now extensively used for drug and material discovery programmes. The subsequent development of analytical capabilities to carry out qualitative and quantitative assessment of the compounds generated by HT synthesis as well as their HT screening has led to a dramatic broadening of the scope of HT techniques, ranging from image based analysis techniques to mass spectrometry (MS). Based on the latter, a range of solid phase and solution phase analytical constructs was developed to enable the qualitative and quantitative assessment of mixtures of small compounds, using positive electrospray MS as the sole analytical tool. A version of the construct allowed HT reactivity profiling to be carried out on a range of ten carboxylic acids, ten aldehydes and ten isonitriles in the Ugi 4-component condensation reaction. The effect of various parameters such as the concentration of the monomers on the reactivity was investigated. The elaboration of a HT Hammett parameter assessment method was made possible by the development of an electrophilic version of the construct. The value of the Hammett value was afforded by means of combinatorial Hammett plots and values were successfully evaluated in a HT mode for around thirty anilines with substituents in the meta and para position of the aromatic ring. Finally, analytical constructs were used in an attempt to evaluate enzyme reaction kinetics via the labelling of peptides and small drug fragment with coded constructs, to afford affinity determinations between the enzyme (protease) and peptidic or fragment based substrates.
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Slocum, Laura Elizabeth. "Evaluation of physical chemistry on-line modules." Virtual Press, 2001. http://liblink.bsu.edu/uhtbin/catkey/1221309.

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We have modeled in one-dimension two-dimensional (2-D) quantum wire structures: the notched electron stub tuner (NEST) and the double-notched electron stub tuner (D-NEST). The models consisted of square barriers representing the notches and square wells representing the stubs. We have calculated the transmission coefficient as a function of electron energy and/or device geometries to study electron transport through these quantum wire models. The transfer matrix method was used to calculate the transmission coefficient by utilizing a program written with Mathematica. The program and technique were verified using one-dimensional systems from the literature.We studied the principle of wave interference in the NEST model in the form of intersection points of several curves of the transmission coefficient versus barrier/well separation plotted with no offset. The creation of standing waves, in certain regions of the NEST model, by the interference of incident and reflected waves, gives rise to these intersection points. We have identified features in the conductance curves of the NEST and the transmission coefficient curves of the NEST model (the intersection points) that are very similar and may be explained by the same principle of wave interference.We have studied double-barrier resonant tunneling (DBRT) to assist in our study of the D-NEST model. The resonances in DBRT are attributed to the creation of standing waves between the two barriers for the tunneling and non-tunneling regimes. We attempted to prove the existence of these standing waves by studying the probability density in the D-NEST model. The well of the D-NEST model was scanned down the length of the double-barrier well region to investigate its effect on the transmission coefficient for this purpose. A small square barrier, used as a probe, was also used to study the probability density in the same way as the well was used. Initial scans of the probe above a simple square barrier gave us insight into the possibility of using it to scan for the probability density in the well region. The "over-the-barrier" resonances (attributed to standing waves) were studied in this case.We have developed knowledge of the transmission properties of these models that may aid in the understanding of the electron transport through the 2-D devices. We believe that to "fine tune" the conductance output of the D-NEST device, the second notch should be placed at a location that permits the creation of standing waves, for a specific electron energy value, between the two notches of the device. The "fine tuning" of the conductance output into a square-wave pattern could improve the devices performance as a potential switching mechanism.
Department of Chemistry
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Frank, Robert A. "Physical chemistry of carbothermic reduction of alumina." Thesis, Massachusetts Institute of Technology, 1985. http://hdl.handle.net/1721.1/15150.

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Thesis (M.S.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 1985.
MICROFICHE COPY AVAILABLE IN ARCHIVES AND SCIENCE
Vita.
Bibliography: leaves 177-180.
by Robert A. Frank.
M.S.
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Books on the topic "Physical Chemistry"

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Zarubin, D. Physical chemistry. ru: INFRA-M Academic Publishing LLC., 2016. http://dx.doi.org/10.12737/20894.

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Vemulapalli, G. K. Physical chemistry. Englewood Cliffs, N.J: Prentice-Hall, 1993.

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Atkins, P. W. Physical chemistry. 5th ed. Oxford: Oxford University Press, 1994.

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White, J. Edmund. Physical chemistry. San Diego: Harcourt Brace Jovanovich, 1987.

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Alberty, Robert A. Physical chemistry. 7th ed. Chichester: John Wiley & sons, 1987.

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Silbey, Robert J. Physical chemistry. 4th ed. Hoboken, New Jersey: John Wiley & sons, 2005.

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Levine, Ira N. Physical chemistry. 5th ed. Boston: McGraw Hill, 2002.

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R, Mount A., and Heal M. R, eds. Physical chemistry. [Place of publication not identified]: CRC Press, 2000.

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Atkins, P. W. Physical chemistry. 4th ed. Oxford: Oxford University Press, 1990.

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R, Mount A., and Heal M. R, eds. Physical chemistry. Oxford, UK: Bios, 2000.

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Book chapters on the topic "Physical Chemistry"

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Hudson, John. "Physical Chemistry." In The History of Chemistry, 202–27. London: Macmillan Education UK, 1992. http://dx.doi.org/10.1007/978-1-349-22362-6_13.

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Hudson, John. "Physical Chemistry." In The History of Chemistry, 202–27. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4684-6441-2_13.

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Kotyk, Arnošt. "Physical Chemistry." In Quantities, Symbols, Units, and Abbreviations in the Life Sciences, 31–33. Totowa, NJ: Humana Press, 1999. http://dx.doi.org/10.1007/978-1-59259-206-7_6.

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Hinrichs, Wouter, and Suzy Dreijer - van der Glas. "Physical Chemistry." In Practical Pharmaceutics, 357–82. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15814-3_18.

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Blake, George R., Gary C. Steinhardt, X. Pontevedra Pombal, J. C. Nóvoa Muñoz, A. Martínez Cortizas, R. W. Arnold, Randall J. Schaetzl, et al. "Physical Chemistry." In Encyclopedia of Soil Science, 555–58. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-3995-9_435.

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Hinrichs, Wouter, and Renske van Gestel. "Physical Chemistry." In Practical Pharmaceutics, 93–125. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-20298-8_6.

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Lewis, Gerald F. "Physical Properties." In Analytical Chemistry, 12–18. London: Macmillan Education UK, 1985. http://dx.doi.org/10.1007/978-1-349-07757-1_5.

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Brandenburg, Klaus, and Thomas Gutsmann. "Lipopolysaccharides: Physical Chemistry." In Encyclopedia of Biophysics, 1306–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_531.

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van der Put, Paul J. "Inorganic Physical Chemistry." In The Inorganic Chemistry of Materials, 345–80. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-0095-1_10.

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Henderson, Douglas J., and Charles T. Rettner. "Physical Chemistry." In Encyclopedia of Physical Science and Technology, 159–76. Elsevier, 2003. http://dx.doi.org/10.1016/b0-12-227410-5/00573-1.

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Conference papers on the topic "Physical Chemistry"

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Stepanovskih, E. I., L. A. Brusnitsina, and T. A. Alekseeva. "Teaching physical chemistry: Electronic labs." In MODERN SYNTHETIC METHODOLOGIES FOR CREATING DRUGS AND FUNCTIONAL MATERIALS (MOSM2020): PROCEEDINGS OF THE IV INTERNATIONAL CONFERENCE. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0068501.

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Spielfiedel, A., N. Feautrier, I. Drira, G. Chambaud, P. Rosmus, and Y. Viala. "Physical chemistry of silicon containing molecules." In The 50th international meeting of physical chemistry: Molecules and grains in space. AIP, 1994. http://dx.doi.org/10.1063/1.46615.

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"Preface: International Conference on Physical Chemistry." In CHEMISTRY BEYOND BORDERS: INTERNATIONAL CONFERENCE ON PHYSICAL CHEMISTRY: The 1st Annual Meeting of the Physical Chemistry Division of the Indonesian Chemical Society. AIP Publishing, 2023. http://dx.doi.org/10.1063/12.0020968.

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Mohan, R. "Weak neutral current chemistry." In Physical orgin of homochirality in life. AIP, 1996. http://dx.doi.org/10.1063/1.51235.

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Sola-Llano, Rebeca, Leire Gartzia-Rivero, Antonio Veloso, Leire Ruiz-Rubio, Leyre Pérez-Álvarez, Jorge Bañuelos, and José Luis Vilas-Vilela. "PHYSICAL CHEMISTRY TOWARDS STRENGTHENING FUTURE CHEMISTS’ AWARENESS OF SUSTAINABILITY: RESEARCH BASED LEARNING." In 14th annual International Conference of Education, Research and Innovation. IATED, 2021. http://dx.doi.org/10.21125/iceri.2021.0746.

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Suh, Yung Doug, and Hyun Woo Kim. "Physical chemistry of Nanogap-Enhanced Raman Scattering (NERS)." In Nanoimaging and Nanospectroscopy V, edited by Prabhat Verma and Alexander Egner. SPIE, 2017. http://dx.doi.org/10.1117/12.2275662.

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Moon, Nicole, G. Grubbs II, and Amanda Duerden. "ROTATIONAL SPECTROSCOPY: A LABORATORY FOR UNDERGRADUATE PHYSICAL CHEMISTRY." In 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.wc09.

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Ellison, B. T., C. T. Gallagher, L. M. Frostman, and S. E. Lorimer. "The Physical Chemistry of Wax, Hydrates, and Asphaltene." In Offshore Technology Conference. Offshore Technology Conference, 2000. http://dx.doi.org/10.4043/11963-ms.

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Tian, Z. W. "Some new applications of physical chemistry to MEMS." In 2010 5th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS 2010). IEEE, 2010. http://dx.doi.org/10.1109/nems.2010.5592516.

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Arpigny, C. "Physical chemistry of comets: Models, uncertainties, data needs." In The 50th international meeting of physical chemistry: Molecules and grains in space. AIP, 1994. http://dx.doi.org/10.1063/1.46600.

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Reports on the topic "Physical Chemistry"

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Frank, Robert A. Physical chemistry of carbothermic reduction of alumina. Office of Scientific and Technical Information (OSTI), September 1985. http://dx.doi.org/10.2172/6570345.

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Mackay, R. A. Physical Chemistry of Exothermic Gas-Aerosol Calaorimetry. Fort Belvoir, VA: Defense Technical Information Center, January 1985. http://dx.doi.org/10.21236/ada150872.

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Maroncelli, Mark. Physical Chemistry of Reaction Dynamics in Ionic Liquid. Office of Scientific and Technical Information (OSTI), October 2016. http://dx.doi.org/10.2172/1327486.

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Margulis, Claudio Javier. Physical Chemistry of Reaction Dynamics in Ionic Liquids. Office of Scientific and Technical Information (OSTI), October 2016. http://dx.doi.org/10.2172/1330584.

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Johnson, C. E., H. M. Attaya, M. C. Billone, R. A. Blomquist, J. P. Kopasz, L. Leibowitz, M. F. Roche, and C. A. Seils. Applied physical chemistry progress report, October 1991--September 1992. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/10146918.

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Luttrell, G. H., R. H. Yoon, and J. B. Zachwieja. Control of pyrite surface chemistry in physical coal cleaning. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/5060937.

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Yoon, R. H., G. H. Luttrell, J. B. Zachwieja, and J. A. Mielczarski. Control of pyrite surface chemistry in physical coal cleaning. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/5474691.

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Blank, David. SISGR: Physical Chemistry of Reaction Dynamics in Ionic Liquids. Office of Scientific and Technical Information (OSTI), October 2017. http://dx.doi.org/10.2172/1405286.

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Castner, Jr., Edward W. SISGR: Physical chemistry of reaction dynamics in ionic liquids. Office of Scientific and Technical Information (OSTI), July 2018. http://dx.doi.org/10.2172/1461643.

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Luttrell, G. H., R. H. Yoon, J. B. Zachwieja, and M. L. Lagno. Control of pyrite surface chemistry in physical coal cleaning. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/5196129.

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