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Relevant bibliographies by topics / Physico-chemical

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Academic literature on the topic 'Physico-chemical'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 July 2024

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Journal articles on the topic "Physico-chemical"

1

Oghly, Jurakulov Sanjar Zafarjon. "PHYSICO-CHEMICAL PROPERTIES OF POLYMER COMPOSITES." American Journal of Applied Science and Technology 3, no. 10 (October 1, 2023): 25–33. http://dx.doi.org/10.37547/ajast/volume03issue10-06.

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The article deals with the role of physics in the modern national economy, production and scientific system. A number of issues are considered, such as physics, the subject of the school curriculum, the methodology of teaching physics, the basics of professional training of a physics teacher, the content and tasks of the methodology of teaching physics, the methodology for studying the methodology of teaching physics, the history of the development of methods of teaching physics.

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Chaabna, Manel, Lina Aissa, Fadhila Debbah, and Nassima Taleb. "Physico-chemical incompatibilities." Batna Journal of Medical Sciences (BJMS) 1, no. 2 (December 31, 2014): 107–10. http://dx.doi.org/10.48087/bjmstf.2014.1212.

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Compatibility problems are frequently encountered in hospitals, particularly in intensive care units. Physico-chemical incompatibilities (PCI) may have different origins and several types. The result is inactivation of the active ingredient reacted training or derivative(s) more or less toxic. The issue of PCI is made complex, moreover, by the fact that the reactions involved may be influenced by many factors. This chemical problem becomes a public health concern because it poses a risk to the patient.

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Ahmad, Rasheed, Shaista Begum, Eric M. V. Hoek, Tanju Karanfil, Esra Ates Genceli, Abhishek Yadav, Paras Trivedi, and Chunlong Carl Zhang. "Physico-Chemical Processes." Water Environment Research 76, no. 6 (September 2004): 823–1002. http://dx.doi.org/10.2175/106143004x142013.

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Ahmad, Rasheed, Shaista Begum, Chunlong Carl Zhang, Tanju Karanfil, Esra Ates Genceli, Abhishek Yadav, and Sirajuddin Ahmed. "Physico-Chemical Processes." Water Environment Research 77, no. 6 (September 2005): 982–1156. http://dx.doi.org/10.2175/106143005x54371.

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Karanfil, Tanju, Abhishek Yadav, Chunlong Carl Zhang, Suman Ghosh, and Sirajuddin Ahmed. "Physico-Chemical Processes." Water Environment Research 78, no. 10 (September 2006): 1193–260. http://dx.doi.org/10.2175/106143006x119198.

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Grenoble, Zlata, Chunlong Carl Zhang, Sirajuddin Ahmed, Stuart B. Jeffcoat, Tanju Karanfil, Meric Selbes, Sehnaz Sule Kaplan, Shaista Begum, and Rasheed Ahmad. "Physico-Chemical Processes." Water Environment Research 79, no. 10 (September 2007): 1228–96. http://dx.doi.org/10.2175/106143007x218395.

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Ahmad, Rasheed, Chunlong Carl Zhang, Sirajuddin Ahmed, Tanju Karanfil, Sehnaz Sule Kaplan, Meric Selbes, and Shaista Begum. "Physico-Chemical Processes." Water Environment Research 80, no. 10 (October 2008): 978–1035. http://dx.doi.org/10.2175/106143008x328554.

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Chelme-Ayala, Pamela, Atefeh Afzal, Parastoo Pourrezaei, Yingnan Wang, Mario A. Zapata, Ning Ding, Jing Jin, Nan Wang, Przemyslaw Drzewicz, and Mohamed Gamal El-Din. "Physico-Chemical Processes." Water Environment Research 81, no. 10 (September 10, 2009): 1056–126. http://dx.doi.org/10.2175/106143009x12445568399451.

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Pourrezaei, Parastoo, Atefeh Afzal, Ning Ding, Md Shahinoor Islam, Ahmed Moustafa, Przemys ł. Aw Drzewicz, Pamela Chelme-Ayala, and Mohamed Gamal El-Din. "Physico-Chemical Processes." Water Environment Research 82, no. 10 (January 1, 2010): 997–1072. http://dx.doi.org/10.2175/106143010x12756668800852.

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Afzal, Atefeh, Parastoo Pourrezaei, Ning Ding, Ahmed Moustafa, Geelsu Hwang, Przemyslaw Drzewicz, Eun-Sik Kim, et al. "Physico-Chemical Processes." Water Environment Research 83, no. 10 (January 1, 2011): 994–1091. http://dx.doi.org/10.2175/106143011x13075599869173.

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Dissertations / Theses on the topic "Physico-chemical"

1

Potužák, Marcel. "Physico-Chemical Properties of Silicate Melts." Diss., lmu, 2006. http://nbn-resolving.de/urn:nbn:de:bvb:19-55228.

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Folmer, Britta M. "Physico-chemical characterisation of novel surfactants /." Stockholm : Tekniska högsk, 2001. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3052.

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Jordan, Peter A. "Physico-chemical studies of aluminium biochemistry." Thesis, University of East Anglia, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294654.

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Lim, Wen Huei. "Physico-chemical properties of ultraflexible vesicles." Thesis, King's College London (University of London), 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.417109.

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Gupta, Saloni. "Physico-chemical properties of polypropylene glycols." Thesis, University of Greenwich, 2015. http://gala.gre.ac.uk/21538/.

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Poly(propylene glycol) (PPG) samples of different molecular mass were characterized using differential scanning calorimetry, modulated differential scanning calorimetry, thermogravimetry and thermally stimulated current (TSC) spectroscopy. It was shown, by TSC, that the glass transition temperature and the degree of molecular mobility increased with increasing molecular mass of PPG. Additional experiments showed that PPGs of molecular mass 425, 1000 and 2000 Da undergo one global relaxation process; however, PPG 2700 (Da) undergoes an additional relaxation process after the glass transition which has been attributed either to the release of the excess charge delocalised in the polymer structure or a liquid-liquid transition. Thermally induced phase separation in aqueous solutions of PPG has been examined using a variety of techniques including high sensitivity scanning calorimetry (HSDSC), hot stage microscopy, small angle neutron scattering, and turbidity measurements. The data suggest that phase separation is a consequence of PPG aggregation (droplets); the aggregates grow in size, as the temperature is raised further. It is postulated that phase separation occurs via nucleation and growth, which is corroborated by model fitting the calorimetric data using a mass action aggregation model. It is concluded that phase separation of PPG occurs as a result of the disruption of a hydrogen bonded network between water and PPG. The effect of five sugars (mannitol, maltose, raffinose, sucrose and trehalose) on the Tm (transition temperature) of aqueous PPG 1000 solutions was studied by HSDSC and turbidity measurements. All the sugars decreased the phase separation temperature of the PPG solutions, with trehalose and maltose showing the greatest effect. A series of experiments, using HPLC, showed that phase separated PPG (1000 Da) increased the apparent aqueous solubility of naphthalene.

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Powell, Francis E. "Physico-chemical studies in flow analysis." Thesis, Loughborough University, 1990. https://dspace.lboro.ac.uk/2134/25925.

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The first part of this study was the characterisation of an impinging jet electrode in an amperometric detector; the device having found extensive application in flow injection analysis. A voltammetric study of the detector in the stopped flow mode was carried out and evidence is presented of restricted diffusion imposed by the shallow depth of the cell. In hydrodynamic voltammetry, the detector exhibited a gradual progression from thin-layer to wall jet behaviour as the flow rate increased. This gradation is discussed in terms of a model in which flow in the electrode chamber forms concentric rings, the streamlines being successively perpendicular, oblique and parallel to the electrode. The response of the detector and its associated equipment was studied by two experiments. Firstly, the fidelity of the electrochemical instrumentation and recording system was ascertained from its electronic response to a RC (resistance-capacitance) circuit functioning as a flow injection transport analogue. Secondly, the dynamic response of the electrochemical cell was established from an experiment using a concentration step input delivered through a short, straight manifold. The results indicated that laminar flow in the delivery tube was modified by mixing stages in the cell channel and its connections to produce a final dispersion which defines an effective detection volume of only 7μL. The electronic and cell responses indicate that the total detection system would impose little extra dispersion in a practical flow injection line. In the second part of this study, photometric titrations were carried out in a stirred tank reactor in which the volume changed linearly with time. The general relation for the concentration gradient when the tank is used as a mixing device was examined experimentally under various flow conditions. In particular, the precision of linear concentration gradients was ascertained when peristaltic pumping was employed. These gradients were utilised to titrate analyte within the tank by means of titrant delivered by pump flow with photometric detection in an exit stream. Self-indicating titrations, following changes in the absorbance of analyte, titrant or reaction product, were performed each conforming to theoretical prediction. Due to the external detection system employed, dispersion and transportation lag effects were observed and accounted for.

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Díez, Orrite Silvia. "Physico-chemical properties of polymers at interfaces." Doctoral thesis, Universitat Rovira i Virgili, 2002. http://hdl.handle.net/10803/8511.

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A polymer is a large molecule constructed from many smaller structural units called
monomers joined together by covalent bonds. Polymers have existed in natural form
since life began and those such as DNA, RNA, proteins and polysaccharides are some
of the most important macromolecules found in plant and animal life. From the earliest
times, the man has used many of these polymers as materials for providing clothing,
decoration, tools, weapons and other requirements. However, the origins of today's
polymer industry commonly are accepted as being in the nineteenth century when
important discoveries were made concerning to the modification of certain natural
polymers, as cellulose. The use of synthetic and natural polymers as stabilisers for
colloid systems (sols, dispersions, microemulsions, etc.) is becoming more important
everyday in contemporary life. Polymer additives can be applied in preconcentrations
and dehydration of suspensions in mineral processing, purification of wastewater and
even in nutritional and pharmaceutical emulsions being their importance related to the
characteristics of the process and the properties that they show. The present work aims
to develop appropriate numerical and analytical modelling techniques, which can
describe (considering the formation of loops and tails) the structure of a polymeric layer
adsorbed on heterogeneous surfaces; this adsorbed layer is an relevant factor in the
properties showed by this kind of materials. Taking into account this, the methodology
known as Single Chain Mean Field (SCMF) (originally used to study micellar
aggregates and grafted polymers) was modified to apply on polymer adsorption
problems. In this way, it was possible to calculate numerically properties that can be
experimentally measured, such as total monomer volume fraction profiles, loop and tail
volume fraction profiles, adsorbance or the thickness of the adsorbed layer. The
structure of the polymeric layer was examined both for flat and spherical (colloidal
particles) surface geometries. When compared with other well established
methodologies for the numerical simulation of polymeric systems, this new version of
SCMF was found to be more efficient due to the improved sampling of the polymer
chain configuration space.
Thus, SCMF method results, in the case of the adsorption on flat surfaces, compare well
with those obtained either with Monte Carlo simulations or with the method developed
in the 80s by Scheutjens and Fleer (SCF). Due to the lack of studies focusing to polymer
adsorption on colloidal particles, our results have been the first to present quantitative
predictions of the structure of the polymeric layer adsorbed on a spherical surface. Thus,
we have demonstrated the dependence of the adsorbed polymer layer with the size of
the colloidal particle as well as the characteristic lengths that influence on it. Finally, in
this work an analytical approach for the description of polymer-colloidal mixtures has
been developed which compares well with the numerical results obtained from the
SCMF methodology. Furthermore, the analytical approach is able to predict system
behaviours, as for example the formation of gels.
Un polímero es una molécula de grandes dimensiones formada de pequeñas unidades
llamadas monómeros, los cuales se encuentran unidos por medio de enlaces covalentes.
Los polímeros han existido de forma natural desde el comienzo de la vida, y aquellos
como el DNA, RNA o las proteínas son algunos de los polímeros más importantes
encontrados tanto en la vida animal como en la vegetal. Desde siempre el hombre ha
utilizado muchos de estos polímeros como materiales para hacer ropa, decoración,
herramientas, etc. Sin embargo, el origen de la industria de polímeros que conocemos
hoy en día se produjo en el siglo 19, gracias a importantes descubrimientos dentro de la
modificación de ciertos polímeros naturales, como la celulosa. El uso de polímeros
sintéticos y naturales como estabilizadores de sistemas coloidales (dispersiones,
microemulsiones, etc.) juega en nuestros días un papel importante. Los polímeros
utilizados como aditivos, pueden ser aplicados en preconcentraciones y deshidratación
de suspensiones dentro de procesos minerales, tratamiento de aguas residuales e incluso
los podemos encontrar dentro de la industria farmacéutica y alimentaria, donde su
importancia es debida a la procesabilidad y propiedades que ellos exhiben. El trabajo
que se presenta es orientado al desarrollo de técnicas de modelización, tanto analíticas
como computacionales, y su aplicación en la descripción (por medio de la formación de
bucles y colas) de la estructura de la capa de polímeros adsorbida en superficies
heterogéneas, siendo dicha capa de polímeros un factor importante en las propiedades
que este tipo de materiales presentan. Con este propósito, la metodología conocida
como Single Chain Mean Field, utilizada anteriormente tanto para el estudio de
agregados micelares como de polímeros anclados en superficies, ha sido modificada
para describir la adsorción de polímeros en superficies. Así se han podido calcular
numéricamente propiedades medibles experimentalmente como los perfiles de la
fracción en volumen de monómeros totales, además de los pertenecientes a los bucles y
colas, adsorbancia o el espesor de la capa adsorbida, para geometrías de la superficie
absorbente tanto plana como esférica (partículas coloidales). En su comparación con
otras metodologías, ya establecidas para la simulación numérica dentro de la física de
polímeros, la aplicación de esta nueva versión del Single Chain Mean Field (SCMF)
ha resultado ser más eficiente debido a un mejor muestreo del espacio de
configuraciones de las cadenas poliméricas. De este modo, comparando los resultados
obtenidos a partir del SCMF, con aquellos obtenidos mediante técnicas de simulación
Monte Carlo o la teoría desarrollada en los años 80 por Scheutjens y Fleer (SCF), se ha
podido encontrar un buen acuerdo en las propiedades calculadas para el caso de la
adsorción en superficies planas. Debido a la dificultad intrínseca del estudio de la
adsorción en superficies curvadas, nuestros resultados son los primeros que presentan
predicciones cuantitativas sobre la estructura de la capa que se forma sobre una
partícula coloidal. Así hemos podido comprobar la dependencia de la estructura de la
capa de polímeros adsorbidos con el tamaño de la partícula sobre la que se encuentran
adsorbidos además de las longitudes características de las cuales depende. Finalmente,
en este trabajo se ha desarrollado, también, una teoría analítica para la descripción de la
mezcla polímero-coloide. De este modo, los resultados numéricos obtenidos con el
SCMF han podido ser comparados con dicha teoría, obteniendo, de nuevo, un buen
acuerdo y predecir, además, comportamientos colectivos como la formación de geles.

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Sellaturay, S. V. "Physico-chemical basis for struvite stone formation." Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1336882/.

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Introduction: Struvite stones (magnesium ammonium phosphate) account for 10-15% of renal stones and can grow rapidly forming staghorn calculi. With limited medical therapies available and surgery the mainstay of treatment, an understanding of the physico-chemical conditions causing struvite crystallization allows development of strategies to prevent their formation. At present, very little is known about the physico-chemical conditions that result in struvite crystallisation. This lack of understanding has two bases: i) the particular ionised concentrations of the reactants (e.g. Mg2+, NH4+, and phosphate) in the urine are unknown; ii) the prevailing chemical conditions that would modulate crystallisation are also unclear (e.g. pH, osmolality, other urinary constituents).Recent advances in the development of ion-selective electrodes allows accurate determination of urinary constituents in small (<1ml) undiluted samples. Methods: We have furthered developed an NH4+-ion selective electrode and magnesium ion-selective electrode to measure the urinary concentrations of each to aid our understanding of struvite deposition. [NH4+] and [Mg2+] were measured using plastic dip cast ion-selective electrodes dispersed in suitable plasticisers, using nonactin for NH4+ and several different neutral ligands for Mg2+. Data were validated against standardised and developing methodology, including colour spectrophotometry and computational algorithms. Urine samples were also subjected to analysis using clinical biochemical techniques. Results: We characterised an NH4+-ion selective electrode and made the first measurements of [NH4+] in undiluted urine samples, in normal subjects and those with stone disease. This technique was validated using colour spectrophotometry and then the technique was used to validate a computational algorithm. We have developed and characterised the Mg2+-ion-selective electrode but Ca2+ caused significant interference. Conclusions: Direct measurement of the urinary [NH4+] has been achieved for the first time with a value of about 25mM. This exciting new technique may now provide clinicians with an important point-of-care investigative tool in diagnosing and monitoring struvite calculogenesis.

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Maciejczyk, Malgorzata. "1,3,2-Benzodiazaboroles : synthetic and physico-chemical studies." Pau, 2010. http://www.theses.fr/2010PAUU3008.

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There is considerable current interest in conjugated organic compounds containing threecoordinate boryl substituents as π-acceptors, as the vacant pz-orbital on boron is capable of significant interaction with an organic π-system. But as boron is less electronegative than carbon, the boryl moiety may also act as α-donor. These boron containing compounds exhibit intriguing fluorescence emission, second and third order non-linear optical properties and fluoride sensing ability. They can serve as emissive and/or electron-transport layers in organic light emitting devices (OLED). Materials with phenylethynyl scaffolds as π-electron conducting units have been intensively studied according to optical and physical properties of oligo- and poly-(p-arylene)ethynes, including those substituted by donor- and/or acceptor functions. This work is followed in collaboration with Pr Weber group at Bielefeld University, which has a long-standing interest in the chemistry of 1,3,2-diazaboroles. Thereby, our studies were carried out on syntheses and the electronic properties of simples and progressively extended π-conjugated systems with 1,3,2-diazaborolyl- and 1,3,2-benzodiazaborolyl- substituents, with the particular interest focused on the influence of substituents on the spectroscopic properties when additional donor functionalities are present in the molecules. Quantum chemical calculations [DFT, TD-DFT, OVGF] have been applied to provide information on the physico-chemical properties and electronic structure of following molecules: 1,3-Diethyl-1,3,2-diazaboroles, 1,3-Diethyl-1,3,2-benzodiazaboroles, 2-Arylethynyl-1,3,-diethyl-1,3,2-benzodiazaboroles, 2[3’-cyano-4’-phenylethynyl]phenyl-1,3,-diethyl-1,3,2-benzodiazaboroles, and finally N-carbazolyl- and Ncarbazolyl-2’-thienyl- functionalized
Il existe actuellement un intérêt considérable pour les composés organiques conjugués contenant des ligands avec l’atome de bore en tant que π accepteur, puisque l’orbitale pz vacante de cet atome peut interagir de manière significative avec un système π organique. Mais comme le bore est moins électronégatif que le carbone, il peut aussi agir comme α-donneur. Il s’avère que ces composés sont doués de propriétés particulièrement intéressantes du point de vue de l’optique non linéaire de second et de troisième ordre. Ils peuvent servir d'émetteur et/ou de transporteur d’électron dans les couches organiques dans les diodes électroluminescentes (OLED). Les matériaux avec le groupement phenyléthynyl en tant que unité de transport d’électrons π a été intensivement étudié par rapport à leurs propriétés optiques et physiques comme oligo- et poly-(p-arylene)ethynes, en incluant ceux substitués par des fonctions donneur - et/ou accepteur. Ce travail est mené en collaboration avec le groupe du Pr Weber de l'Université Bielefeld, qui s’intéresse de longue date à la chimie des 1,3,2-diazaboroles. Ainsi, nos études ont portées sur les synthèses et les propriétés électroniques de systèmes π conjugués simples et ont progressivement été étendues aux substituants 1,3,2-diazaborolyl- et 1,3,2-benzodiazaborolyl, avec un intérêt particulier sur l'influence de substituants sur les propriétés spectroscopiques quand les fonctions additionnelles donneurs sont présentes dans les molécules. Les calculs quantiques [DFT,TD-DFT,OVGF] ont été effectués pour obtenir des renseignements sur les propriétés physico-chimiques et la structure électronique de molécules suivantes : 1,3-diéthyl-1,3,2-diazaboroles, 1,3-diéthyl-1,3,2-benzodiazaboroles, 2-aryléthynyl-1,3,-diéthyl-1,3,2-benzodiazaboroles, 2[3’-cyano-4’-phényléthynyl]phenyl-1,3,-diéthyl-1,3,2-benzodiazaboroles et finalement N-carbazolyl-et N-carbazolyl-2’-thiényl-functionalized compounds

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Kalogianni, Eleni P. "Physico-chemical and chemical changes during repeated deep-frying of potatoes." Thesis, University of Lincoln, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.441670.

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Books on the topic "Physico-chemical"

1

Vakula, V. L. Polymer adhesion: Physico-chemical principles. Edited by Pritykin L. M, Vakula Alexander V, and Catterall Eric. New York: E. Horwood, 1991.

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Peters, A. T. Physico-Chemical Principles of Color Chemistry. Dordrecht: Springer Netherlands, 1996.

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Beckett, S. T., ed. Physico-Chemical Aspects of Food Processing. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1227-7.

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Restelli, G., and G. Angeletti, eds. Physico-Chemical Behaviour of Atmospheric Pollutants. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0567-2.

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Burkinshaw, Stephen M. Physico-chemical Aspects of Textile Coloration. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118725658.

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Angeletti, G., and G. Restelli, eds. Physico-Chemical Behaviour of Atmospheric Pollutants. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3841-0.

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Peters, A. T., and H. S. Freeman, eds. Physico-Chemical Principles of Color Chemistry. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0091-2.

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Ranga, Narayanan, and COSPAR, eds. Gravitational effects in physico-chemical processes. Oxford: Published for the Committee on Space Research [by] Pergamon, 2003.

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T, Peters A., and Freeman H. S, eds. Physico-chemical principles of color chemistry. London: Blackie Academic & Professional, 1996.

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T, Beckett S., ed. Physico-chemical aspects of food processing. London: Blackie Academic & Professional, 1995.

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Book chapters on the topic "Physico-chemical"

1

Baker, Julien S., Fergal Grace, Lon Kilgore, David J. Smith, Stephen R. Norris, Andrew W. Gardner, Robert Ringseis, et al. "Physico-chemical." In Encyclopedia of Exercise Medicine in Health and Disease, 711. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_2875.

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Vekshin, Nikolai. "Physico-Chemical Mechanisms." In Biophysics of Mitochondria, 49–72. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-33853-4_4.

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Bennett, Richard H., and Matthew H. Hulbert. "Physico-Chemical Interactions." In Clay Microstructure, 5–45. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4684-2_2.

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Osadchyy, Volodymyr, Bogdan Nabyvanets, Petro Linnik, Nataliia Osadcha, and Yurii Nabyvanets. "Physico-Chemical Processes." In Processes Determining Surface Water Chemistry, 69–163. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-42159-9_3.

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Holzbach, R. T., R. L. Barnhart, and J. M. Nader. "The Physico-chemical Defect." In Bile Acids in Health and Disease, 117–33. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1249-6_8.

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Clarke, J. F. "Physico-Chemical Gas Dynamics." In Kinetic Theory and Gas Dynamics, 135–82. Vienna: Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-2762-9_5.

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Soustelle, Michel. "Physico-Chemical Transformations and Equilibria." In Chemical Equilibria, 1–24. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119178545.ch1.

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Oliveira, D. R. "Physico-Chemical Aspects of Adhesion." In Biofilms — Science and Technology, 45–58. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-1824-8_5.

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Bacri, J. C., R. Perzynski, D. Salin, V. Cabuil, R. Massart, J. N. Pons, and J. Roger. "Ionic Ferrofluids: Physico-Chemical Aspects." In Springer Proceedings in Physics, 59–64. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71526-6_11.

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Pirumov, Ul’yan G., and Gennadi S. Roslyakov. "Flows with Physico-Chemical Transformations." In Gas Flow in Nozzles, 199–317. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-86790-3_6.

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Conference papers on the topic "Physico-chemical"

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van Oort, Eric. "Physico-Chemical Stabilization of Shales." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1997. http://dx.doi.org/10.2118/37263-ms.

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Ignaci Victoria Thiagarajan, Venkatesh Meda, and Phyllis Shand. "PHYSICO-CHEMICAL CHARACTERISTICS OF BEEF JERKY." In 2006 CSBE/SCGAB, Edmonton, AB Canada, July 16-19, 2006. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2006. http://dx.doi.org/10.13031/2013.22119.

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Luma, Kosovare, Arleta Rifati-Nixha, Fatjona Isufaj, and Miribane Dërmaku-Sopjani. "Physico - chemical properties of almond oil." In University for Business and Technology International Conference. Pristina, Kosovo: University for Business and Technology, 2018. http://dx.doi.org/10.33107/ubt-ic.2018.185.

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Grigoreva, Liudmila. "PHYSICO-CHEMICAL METHOD OF ENHANCED OIL RECOVERY." In 16th International Multidisciplinary Scientific GeoConference SGEM2016. Stef92 Technology, 2016. http://dx.doi.org/10.5593/sgem2016/b13/s06.113.

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Abramov, A. "Physico-chemical fundamentals of nonsulphide minerals flotation." In The 8th International Mineral Processing Symposium. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2017. http://dx.doi.org/10.4324/9780203747117-38.

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I. Svarovskaya, L., L. K. Altunina, and Z. A. Rozhenkova. "Combined Physico-Chemical and Microbiological EOR Method." In IOR 1999 - 10th European Symposium on Improved Oil Recovery. European Association of Geoscientists & Engineers, 1999. http://dx.doi.org/10.3997/2214-4609.201406327.

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Altunina, L. K., and V. A. Kuvshinov. "Evolution Tendencies of Physico-Chemical EOR Methods." In SPE European Petroleum Conference. Society of Petroleum Engineers, 2000. http://dx.doi.org/10.2118/65173-ms.

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Klinskaya, N., V. Jilyaev, and A. Pankratov. "Physico-Chemical Aspects of Plasma Spray Coatings." In ITSC 1998, edited by Christian Coddet. ASM International, 1998. http://dx.doi.org/10.31399/asm.cp.itsc1998p0747.

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Abstract The results of an investigation into compound, structure and some properties of composite plasma coatings based on stellite with an addition of titanium nitride are presented. It is shown that the coating formed in a gas-air plasma is characterized by better wear resistance and resistance to scaling. The results of industrial test lend support to wide use of such coatings in machine parts and units that work under the simultaneous influence of impact, abrasive wear and high temperature.

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Srieko, Khongsak, Dagva Ariunzaya, and Ulziibat Gantogoo. "Physico-chemical properties of rice starch gel." In 2012 7th International Forum on Strategic Technology (IFOST). IEEE, 2012. http://dx.doi.org/10.1109/ifost.2012.6357809.

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Smagulova, A. Sh. "Physico-chemical analysis of imported dietary supplements." In XX Anniversary All-Russian Scientific and Practical Conference of Young Scientists, Postgraduates and Students. Technical Institute (BRANCH) of NEFU, 2019. http://dx.doi.org/10.18411/s-2019-77.

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Reports on the topic "Physico-chemical"

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Sivashinsky, G. Topics in physico-chemical hydrodynamics. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/5829181.

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Sivashinsky, G. Topics in physico-chemical hydrodynamics. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/6490638.

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Six, Johan, and Alain F. Plante. Physico-chemical and Bio-chemical Controls on Soil C Saturation Behavior. Office of Scientific and Technical Information (OSTI), May 2011. http://dx.doi.org/10.2172/1015558.

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Michalske, T. A., D. R. Jennison, P. J. Feibelman, J. E. Houston, and G. L. Kellogg. Physico-chemical stability of solid surfaces: Final report. Office of Scientific and Technical Information (OSTI), June 1998. http://dx.doi.org/10.2172/654202.

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Cheng, M. D. Physico-Chemical Dynamics of Nanoparticle Formation during Laser Decontamination. Office of Scientific and Technical Information (OSTI), June 2005. http://dx.doi.org/10.2172/893273.

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Cheng, M. D. Physico-Chemical Dynamics of Nanoparticle Formation during Laser Decontamination. Office of Scientific and Technical Information (OSTI), June 2004. http://dx.doi.org/10.2172/839150.

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Peter J. Ortoleva. Automated Physico-Chemical Cell Model Development through Information Theory. Office of Scientific and Technical Information (OSTI), November 2005. http://dx.doi.org/10.2172/860659.

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Cheng, Meng-Dawn. PHYSICO-CHEMICAL DYNAMICS OF NANOPARTICLE FORMATION DURING LASER DECONTAMINATION AND CHARACTERIZATION. Office of Scientific and Technical Information (OSTI), June 2002. http://dx.doi.org/10.2172/835402.

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Cheng, Meng-Dawn. PHYSICO-CHEMICAL DYNAMICS OF NANOPARTICLE FORMATION DURING LASER DECONTAMINATION AND CHARACTERIZATION. Office of Scientific and Technical Information (OSTI), June 2003. http://dx.doi.org/10.2172/835403.

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Kumar, Devendra, and S. P. McGlynn. A Physico-Chemical Study of Some Areas of Fundamental Significance to Biophysics. Office of Scientific and Technical Information (OSTI), April 1999. http://dx.doi.org/10.2172/7144.

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