Relevant bibliographies by topics / Chemical engineering. Chemistry. Biochemistry

Contents

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

Academic literature on the topic 'Chemical engineering. Chemistry. Biochemistry'

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

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Journal articles on the topic "Chemical engineering. Chemistry. Biochemistry"

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Jeguirim, Mejdi, and Lionel Limousy. "International Chemical Engineering Congress 2013: From fundamentals to applied chemistry and biochemistry." Comptes Rendus Chimie 18, no. 1 (2015): 11–14. http://dx.doi.org/10.1016/j.crci.2014.11.009.

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Harrowfield, Jack M. "Biological coordination chemistry, a confluence of chemistry and biochemistry." Comptes Rendus Chimie 8, no. 2 (2005): 199–210. http://dx.doi.org/10.1016/j.crci.2004.12.001.

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Fitzpatrick, D. E., and S. V. Ley. "Engineering chemistry for the future of chemical synthesis." Tetrahedron 74, no. 25 (2018): 3087–100. http://dx.doi.org/10.1016/j.tet.2017.08.050.

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Sheldon, Roger A. "Engineering a more sustainable world through catalysis and green chemistry." Journal of The Royal Society Interface 13, no. 116 (2016): 20160087. http://dx.doi.org/10.1098/rsif.2016.0087.

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The grand challenge facing the chemical and allied industries in the twenty-first century is the transition to greener, more sustainable manufacturing processes that efficiently use raw materials, eliminate waste and avoid the use of toxic and hazardous materials. It requires a paradigm shift from traditional concepts of process efficiency, focusing on chemical yield, to one that assigns economic value to replacing fossil resources with renewable raw materials, eliminating waste and avoiding the use of toxic and/or hazardous substances. The need for a greening of chemicals manufacture is readily apparent from a consideration of the amounts of waste generated per kilogram of product (the E factors) in various segments of the chemical industry. A primary source of this waste is the use of antiquated ‘stoichiometric’ technologies and a major challenge is to develop green, catalytic alternatives. Another grand challenge for the twenty-first century, driven by the pressing need for climate change mitigation, is the transition from an unsustainable economy based on fossil resources—oil, coal and natural gas—to a sustainable one based on renewable biomass. In this context, the valorization of waste biomass, which is currently incinerated or goes to landfill, is particularly attractive. The bio-based economy involves cross-disciplinary research at the interface of biotechnology and chemical engineering, focusing on the development of green, chemo- and biocatalytic technologies for waste biomass conversion to biofuels, chemicals and bio-based materials. Biocatalysis has many benefits to offer in this respect. The catalyst is derived from renewable biomass and is biodegradable. Processes are performed under mild conditions and generally produce less waste and are more energy efficient than conventional ones. Thanks to modern advances in biotechnology ‘tailor-made’ enzymes can be economically produced on a large scale. However, for economic viability it is generally necessary to recover and re-use the enzyme and this can be achieved by immobilization, e.g. as solid cross-linked enzyme aggregates (CLEAs), enabling separation by filtration or centrifugation. A recent advance is the use of ‘smart’, magnetic CLEAs, which can be separated magnetically from reaction mixtures containing suspensions of solids; truly an example of cross-disciplinary research at the interface of physical and life sciences, which is particularly relevant to biomass conversion processes.
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Shimizu, Y., Sandeep Gupta, Kazuo Masuda, Lucie Maranda, C. K. Walker, and R. Wang. "Dinoflagellate and other microalgal toxins: chemistry and biochemistry." Pure and Applied Chemistry 61, no. 3 (1989): 513–16. http://dx.doi.org/10.1351/pac198961030513.

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Raven, E. Lloyd, A. Celik, P. M. Cullis, R. Sangar, and M. J. Sutcliffe. "Engineering the active site of ascorbate peroxidase." Biochemical Society Transactions 29, no. 2 (2001): 105–11. http://dx.doi.org/10.1042/bst0290105.

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Understanding the catalytic versatility of haem enzymes, and in particular the relationships that exist between different classes of haem-containing proteins and the mechanisms by which the apo-protein structure controls chemical reactivity, presents a major experimental and theoretical challenge. These issues are discussed in the general context of peroxidase and cytochrome P450 chemistry, and specific issues relating to the catalytic chemistry of ascorbate peroxidase are highlighted.
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Tsipis, Athanassios C. "Correction: DFT/TDDFT insights into the chemistry, biochemistry and photophysics of copper coordination compounds." RSC Advances 10, no. 63 (2020): 38251. http://dx.doi.org/10.1039/d0ra90110e.

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Correction for ‘DFT/TDDFT insights into the chemistry, biochemistry and photophysics of copper coordination compounds’ by Athanassios C. Tsipis, RSC Adv., 2014, 4, 32504–32529, DOI: 10.1039/C4RA04921G.
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Schmickler, Wolfgang. "The Jerusalem symposia on quantum chemistry and biochemistry." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 234, no. 1-2 (1987): 369. http://dx.doi.org/10.1016/0022-0728(87)80186-9.

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Tsipis, Athanassios C. "DFT/TDDFT insights into the chemistry, biochemistry and photophysics of copper coordination compounds." RSC Advances 4, no. 61 (2014): 32504–29. http://dx.doi.org/10.1039/c4ra04921g.

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Maksić, Zvonimir B., and Robert Vianello. "Physical origin of chemical phenomena: Interpretation of acidity, basicity, and hydride affinity by trichotomy paradigm." Pure and Applied Chemistry 79, no. 6 (2007): 1003–21. http://dx.doi.org/10.1351/pac200779061003.

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Some of the most important aspects of modeling in chemistry are discussed in detail. It is argued that the interpretive side of (quantum) chemistry is indispensable, since it gives sense to a myriad of experimental and computational results. The usefulness of some physical modeling is illustrated by the trichotomy approach in rationalizing acidity, basicity, and hydride affinities of neutral organic compounds. According to trichotomy paradigm, the simple chemical reaction of protonation and H- attachment can be decomposed into three separate sequential steps, which in turn mirror the initial-, intermediate-, and final-state effects. Ample evidence is given, which convincingly shows that the trichotomy approach has some distinct advantages in interpreting aforementioned properties that belong to the most important ones in chemistry and biochemistry.
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Dissertations / Theses on the topic "Chemical engineering. Chemistry. Biochemistry"

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Smith, Gregory K. "Simulations of chemical catalysis." Thesis, The University of New Mexico, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3612623.

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<p> This dissertation contains simulations of chemical catalysis in both biological and heterogeneous contexts. A mixture of classical, quantum, and hybrid techniques are applied to explore the energy profiles and compare possible chemical mechanisms both within the context of human and bacterial enzymes, as well as exploring surface reactions on a metal catalyst. A brief summary of each project follows. </p><p> Project 1 - Bacterial Enzyme SpvC </p><p> The newly discovered SpvC effector protein from <i>Salmonella typhimurium </i> interferes with the host immune response by dephosphorylating mitogen-activated protein kinases (MAPKs) with a &beta;-elimination mechanism. The dynamics of the enzyme substrate complex of the SpvC effector is investigated with a 3.2 ns molecular dynamics simulation, which reveals that the phosphorylated peptide substrate is tightly held in the active site by a hydrogen bond network and the lysine general base is positioned for the abstraction of the alpha hydrogen. The catalysis is further modeled with density functional theory (DFT) in a truncated active-site model at the B3LYP/6-31 G(d,p) level of theory. The truncated model suggested the reaction proceeds via a single transition state. After including the enzyme environment in <i>ab initio</i> QM/MM studies, it was found to proceed via an E1cB-like pathway, in which the carbanion intermediate is stabilized by an enzyme oxyanion hole provided by Lys104 and Tyr158 of SpvC. </p><p> Project 2 - Human Enzyme CDK2 </p><p> Phosphorylation reactions catalyzed by kinases and phosphatases play an indispensable role in cellular signaling, and their malfunctioning is implicated in many diseases. Ab initio quantum mechanical/molecular mechanical studies are reported for the phosphoryl transfer reaction catalyzed by a cyclin-dependent kinase, CDK2. Our results suggest that an active-site Asp residue, rather than ATP as previously proposed, serves as the general base to activate the Ser nucleophile. The corresponding transition state features a dissociative, metaphosphate-like structure, stabilized by the Mg(II) ion and several hydrogen bonds. The calculated free-energy barrier is consistent with experimental values. </p><p> Project 3 - Bacterial Enzyme Anthrax Lethal Factor </p><p> In this dissertation, we report a hybrid quantum mechanical and molecular mechanical study of the catalysis of anthrax lethal factor, an important first step in designing inhibitors to help treat this powerful bacterial toxin. The calculations suggest that the zinc peptidase uses the same general base-general acid mechanism as in thermolysin and carboxypeptidase A, in which a zinc-bound water is activated by Glu687 to nucleophilically attack the scissile carbonyl carbon in the substrate. The catalysis is aided by an oxyanion hole formed by the zinc ion and the side chain of Tyr728, which provide stabilization for the fractionally charged carbonyl oxygen. </p><p> Project 4 - Methanol Steam Reforming on PdZn alloy </p><p> Recent experiments suggested that PdZn alloy on ZnO support is a very active and selective catalyst for methanol steam reforming (MSR). Plane-wave density functional theory calculations were carried out on the initial steps of MSR on both PdZn and ZnO surfaces. Our calculations indicate that the dissociation of both methanol and water is highly activated on flat surfaces of PdZn such as (111) and (100), while the dissociation barriers can be lowered significantly by surface defects, represented here by the (221), (110), and (321) faces of PdZn. The corresponding processes on the polar Zn-terminated ZnO(0001) surfaces are found to have low or null barriers. Implications of these results for both MSR and low temperature mechanisms are discussed.</p>
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Barriga, Jeffrey. "Characterization of the emulsifying mannoproteins of Saccharomyces cerevisiae." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=23364.

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Mannoproteins from Saccharomyces cerevisiae (Baker's yeast) were extracted in high yield. The crude extract was resolved into two components, $ alpha$ and $ beta$, using capillary electrophoresis. These were both shown to be fragments from the cell wall mannoproteins. The $ alpha$ component consisted mainly of the protein portion of the mannoproteins and the $ beta$ component consisted of the long highly phosphorylated mannan chains. Fragmentation occurred when the covalent bonds between the mannans and the asparagine residues were hydrolysed during the hot citrate extraction procedure.<br>The $ alpha$ component was identified as the active emulsifying agent. Although the $ beta$ component was not an emulsifier, it was an effective coemulsifier and improved the properties of the $ alpha$ component.<br>The emulsifying properties of these materials were related to the ability to bind the dye Coomassie blue. Removal of the long mannan chains both increases emulsifying ability and exposes the protein chain for binding to the dye.
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Garofalo, Flavio A. (Flavio Alberto). "Serum cholesterol depletion using immobilized pseudomonas pictorum." Thesis, McGill University, 1989. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=74354.

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Pseudomonas pictorum can deplete serum cholesterol. Cholesterol depleted includes free cholesterol, esterified cholesterol and cholesterol bound to different lipoproteins. Temporarily accumulated cholestenone was metabolized as reaction continued. The reaction kinetics controls the global cholesterol depletion rate during the initial part of the fermentation. Then, mass transfer takes control. In the latter, the global rate was first order with respect to the cholesterol concentration and zero order with respect to the bacterial concentration. The half time was 330 min. The activation energy was 83 kJ/mol. These results are consistent with the aqueous cholesterol diffusion model. P. pictorum was immobilized in alginate beads, polylysine microcapsules and open pore agar beads. The latter depleted serum cholesterol. The depletion rates were similar to those of free P. pictorum, suggesting a barrier free mass transfer. The matrix effect diffusivity for lipoproteins at 37$ sp circ$C was 6.7 $ times$ 10$ sp{-11}$ m$ sp2$/s. The beads effectively retained P. pictorum. No leakage was detected.
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Marin, Joseph R. "Production of sophorolipids from long-chain fatty acids by candida bombicola." Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=79250.

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Tall oil, a mixture of long-chain oleic and linoleic acids, was found to be a suitable lipophilic substrate for the production of sophorolipid, an extracellular glycolipid surfactant, by Candida bombicola ATCC 22214. Oxygen limitation was found to decrease sophorolipid production in this system. Partitioning experiments with sophorolipid revealed that the surfactant increases the affinity of oleic acid for the aqueous phase of a two phase system. C. bombicola therefore has potential applications in the remediation of pulp and paper effluent containing recalcitrant long-chain fatty acids; both for its ability to degrade the acids and for the tendency of sophorolipid to make fatty acids more bioavailable to organisms involved in downstream activated sludge treatment. A novel capillary gas chromatography method was developed to rapidly and quantitatively analyze long-chain fatty acids.
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Gu, Lina. "Heterologous expression of manganese peroxidase from Phanerochaete chrysosporium in Pichia pastoris." Related Electronic Resource: Current Research at SU : database of SU dissertations, recent titles available full text, 2003. http://wwwlib.umi.com/cr/syr/main.

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Aguinaga-Diaz, de Leon Pablo 1965. "Polymers modification with metal chelates and their application to the recovery of metals and biocompounds from aqueous solutions." Thesis, The University of Arizona, 1992. http://hdl.handle.net/10150/278196.

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This work presents the results of studies for protein and metal separations from aqueous solutions by means of metal-chelating interactions using salt-polymer aqueous two-phase systems. Several polymer-chelates were synthesized and characterized. Polyethylene glycol (8000 M.W.) and sodium sulfate along with four different chelates (IDA, TED, Cm-TREN and L-ASP) coupled to monomethoxy polyethylene glycol (M-PEG), were used for the preparation of aqueous two-phase systems and the recovering of metals. The PEG-Chelators synthesized complexed with Cu⁺² Ni⁺² Co⁺² and Zn⁺² were used for the recovery of proteins from aqueous solutions. The influence of the pH, the chelated metal as well as the number of accessible histidine groups on proteins partitioning was investigated and found not to follow a linear relationship for all cases.
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Agarwal, Kitty. "Characterization of cell-secreted microvesicles: modulators of cell-cell communication." The Ohio State University, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=osu1388511983.

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Menegatti, Stefano. "Design, Selection, and Development of Novel Peptide Ligands for Bioseparations and Diagnostics." Thesis, North Carolina State University, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=3575894.

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<p> The relevance of protein-based biopharmaceuticals has increased dramatically in the past decades and a variety of products are now available for human therapy. Antibodies in particular are currently the most heavily consumed protein therapeutics, with a current market volume expected to reach 1 trillion US$ in 2015 and a compound annual growth rate (CAGR) of 3-6%. Meeting the increasing demand for these therapeutics at lower prices while complying with increasingly stringent regulatory environments, calls for the development of new technologies and platform approaches for efficient downstream protein purification. Extended use of affinity chromatography holds great promise in meeting the urgent demand for affordable high-quality biological products. This technology, however, is still dependent on the use of biological ligands, such as Protein A, Protein G, and Protein L, that have significant issues associated with their high cost, harsh elution conditions, narrow specificity, low chemical stability, and immunogenicity in patients if they leach into the product stream. Small, robust, synthetic ligands may offer an effective alternative to protein ligands. Peptides in particular combine levels of affinity and specificity similar to those of biological ligands with high chemical and biochemical stability, broader specificity, low immunogenicity and ease of synthesis that can reduce costs.</p><p> The work in this thesis aims to discover and characterize novel peptide ligands to produce efficient, robust, and affordable affinity adsorbents for improved downstream purification of biologics. Two main areas have been investigated: (a) the development of linear hexapeptide &ndash; based adsorbents for the purification of human antibodies and (b) the design and screening of novel libraries of cyclic peptides for the discovery of novel ligands.</p><p> The research conducted on the characterization and development of competitive peptide-based affinity adsorbents comprises: (a.1) testing existing peptide ligands for the purification of antibodies from a variety of sources; (a.2) optimizing the protocol of ligand coupling on chromatographic resins to increase adsorbent binding capacity; (a.3) a method of modification of the resin&rsquo;s surface chemistry to increase the adsorbent's chemical stability in harsh alkaline conditions; and (a.4.) a combined computational and chemical strategy for the design of protease-stable peptide ligands. The resulting peptide affinity adsorbents compete well with advanced Protein A &ndash; based adsorbents in terms of product yield and purity, dynamic binding capacity (~ 50 &ndash; 60 g/L), resistance to alkaline cleaning and sanitization, and biochemical stability in the presence of proteolytic enzymes.</p><p> In the second part of this work, two methods are presented for the design, synthesis, and screening of libraries of cyclic peptides for the identification of novel affinity ligands. The first method involves the generation and screening of (b.1) a biological mRNA-display library of cyclic peptides, and the second method (b.2) uses a synthetic solid-phase library of &ldquo;reversible cyclic peptides&rdquo;. Both libraries have been screened for the identification of ligands for human antibodies. The results of these studies indicate that these libraries are very promising tools for the discovery of robust, selective and affordable peptide ligands.</p><p> The methods presented herein offer a new set of tools, not only for affinity ligand discovery, but also for finding new drugs and diagnostic methods. Besides their technological value, these studies also offer insights into the mechanisms of non-covalent interaction that underlie the phenomena of biorecognition and protein activity.</p>
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Garcia-Barron, Javier Enrique. "Synthesis and study of chelating polymers and their application to protein and metal separation from aqueous solutions using novel metal affinity interaction techniques." Diss., The University of Arizona, 1999. http://hdl.handle.net/10150/283931.

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The main objective of this research work was the development, synthesis, and study of polymeric chelating derivatives. These derivatives were characterized in terms of their specific metal affinity interaction with biomolecules and metal ions. These engineered materials were used to test their feasibility as tools for separation of proteins and heavy metal ions from aqueous solutions using different affinity separation techniques. Linear and branched polymers were synthesized to create a variety of materials. Among the linear polymers synthesized was the chelated monomethoxy poly(ethylene) glycol (PEG-IDA). This derivative was used in metal affinity partitioning and metal affinity electrophoresis for fast protein-metal interaction analysis. Also a linear heterobifunctional poly(ethylene) glycol (Biotin - PEG - IDA) was synthesized and used as a tool to develop a modified enzyme-linked immuno sorbent assay (ELISA). A multi-armed high molecular weight chelating poly(ethylene) glycol (Star PEG-IDA) was prepared to enhance the separation of protein mixture in gel permeation chromatography. Iminodiacetic poly(ethyleneimine) (PEI-IDA) was prepared and used as a soluble chelating polymer in complexation-ultrafiltration studies for heavy metal ion removal from aqueous solutions. Similar PEIs were also used as casting polymers for the synthesis of affinity adsorbents useful in chromatographic applications. Either as a soluble macromolecule or as a casting polymer for the preparation of adsorbents, PEI chelated derivatives were used for ultratrace metal ion preconcentration and metal ion separations. All polymeric materials prepared were characterized using analytical techniques which include elementary analysis, atomic absorption, UV and IR spectroscopy, high performance liquid chromatography and several colorimetric assays for the determination of end groups and product purity. Metal affinity separation techniques studied with the aforementioned derivatives included: affinity partitioning, affinity electrophoresis and affinity size exclusion for protein purification; affinity complexation-ultrafiltration and metal ion affinity chromatography for removal of heavy metal. Efficient separation of protein mixtures were achieved based on selective affinity by some of the chelated polymers here described and extremely high metal adsorption capacities were found for some of the PEI-based adsorbents prepared. Even though, some of these techniques are still in developmental stages, the results are very promising and encouraging for biotechnical and environmental applications.
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Jouzi, Maryam. "Carbon nanotube nanoneedles and their electrical-mechanical-chemical interactions with biological systems." View abstract/electronic edition; access limited to Brown University users, 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:3318334.

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Books on the topic "Chemical engineering. Chemistry. Biochemistry"

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Keszei, Ernő. Chemical Thermodynamics: An Introduction. Springer Berlin Heidelberg, 2012.

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Press, Apple Academic, ed. Chemical technology: Key developments in applied chemistry, biochemistry and materials science. Apple Academic Press, 2015.

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Piletsky, Sergey A. Designing Receptors for the Next Generation of Biosensors. Springer Berlin Heidelberg, 2013.

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Mirsky, Vladimir M. Ultrathin Electrochemical Chemo- and Biosensors: Technology and Performance. Springer Berlin Heidelberg, 2004.

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Narayanaswamy, Ramaier. Optical Sensors: Industrial Environmental and Diagnostic Applications. Springer Berlin Heidelberg, 2004.

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Osada, Yoshihito. Polymer Sensors and Actuators. Springer Berlin Heidelberg, 2000.

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Cohen, Steven A. Multidimensional liquid chromatography: Theory and applications in industrial chemistry and the life sciences. Wiley-Interscience, 2008.

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Chemical and biochemical technology: Materials, processing, and reliability. Apple Academic Press, 2015.

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Milagro, Reig, and SpringerLink (Online service), eds. Analytical Tools for Assessing the Chemical Safety of Meat and Poultry. Springer US, 2012.

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Andreas, Manz, Zhang Yonghao, and SpringerLink (Online service), eds. Microdroplet Technology: Principles and Emerging Applications in Biology and Chemistry. Springer New York, 2012.

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Book chapters on the topic "Chemical engineering. Chemistry. Biochemistry"

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Hine, F., B. V. Tilak, and K. Viswanathan. "Chemistry and Chemical Engineering in the Chlor-Alkali Industry." In Reviews of Physiology, Biochemistry and Pharmacology. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-1-4613-1791-3_5.

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Szczepanski, R. "Chemical Engineering." In an introduction to Industrial Chemistry. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-6438-6_7.

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Szczepanski, Richard. "Chemical Engineering." In An Introduction to Industrial Chemistry. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-0613-9_8.

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Schultz, M., and H. Kunz. "Chemical and enzymatic synthesis of glycopeptides." In Interface between Chemistry and Biochemistry. Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9061-8_10.

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Zuin, Vânia Gomes, Mateus Lodi Segatto, and Luize Zola Ramin. "Green Chemistry in Analytical Chemistry." In Green Chemistry and Chemical Engineering. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9060-3_1017.

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Meier, Willi. "Chemistry and Chemical Engineering." In Practical Applications of Fuzzy Technologies. Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4601-6_9.

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Inglis, A. S., G. E. Reid, and R. J. Simpson. "Chemical techniques employed for the primary structural analysis of proteins and peptides." In Interface between Chemistry and Biochemistry. Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9061-8_8.

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Mulliken, Robert S., and Bernard J. Ransil. "MIT: Chemistry and Chemical Engineering." In Life of a Scientist. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-61320-3_3.

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Shah, Y. T., A. B. Pandit, and V. S. Moholkar. "Gas-Liquid Cavitation Chemistry." In The Plenum Chemical Engineering Series. Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4787-7_4.

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Filiciotto, Layla, and Rafael Luque. "Nanocatalysis for Green Chemistry." In Green Chemistry and Chemical Engineering. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9060-3_1007.

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Conference papers on the topic "Chemical engineering. Chemistry. Biochemistry"

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GenTan, Xie, Lin Na, Bi ZhiLi, Shan Jie, and LI HongMei. "Application of Molecular Chemistry in Biochemistry and Chemistry and Biology Application of Traditional in Medicine." In 2021 10th International Conference on Applied Science, Engineering and Technology (ICASET 2021). Atlantis Press, 2021. http://dx.doi.org/10.2991/aer.k.210817.013.

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Adams, Joseph P. "Synthetic Biochemistry as a Tool for Sustainable Processing: An Industrial Perspective." In 14th Asia Pacific Confederation of Chemical Engineering Congress. Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-1445-1_589.

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Kresinski, Roman, Seema Pillai, and Peter Foot. "Scorpionates: Coordination Chemistry Comes Home." In Chemical technology and engineering. Lviv Polytechnic National University, 2019. http://dx.doi.org/10.23939/cte2019.01.397.

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Cisneros, Gerardo, J. A. Cogordan, Miguel Castro, and Chumin Wang. "Computational Chemistry and Chemical Engineering." In Third UNAM-CRAY Supercomputing Conference. WORLD SCIENTIFIC, 1997. http://dx.doi.org/10.1142/9789814529426.

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Chrobok, Anna. "Ionic liquids – application driven synthesis in green chemistry." In Chemical technology and engineering. Lviv Polytechnic National University, 2019. http://dx.doi.org/10.23939/cte2019.01.240.

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Москалев, Владимир Борисович. "PREDICTION OF THE CONDITIONS OF CHEMICAL ORGANIC REACTIONS USING THE EDGE ATTENTION GRAPH CONVOLUTION NETWORK." In Наука. Исследования. Практика: сборник избранных статей по материалам Международной научной конференции (Санкт-Петербург, Апрель 2020). Crossref, 2020. http://dx.doi.org/10.37539/srp290.2020.84.35.019.

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Моделирование структуры химической реактивности с точки зрения структуры участвующих веществ имеет важные последствия во всех областях химии и биохимии, от синтеза до понимания метаболических процессов. Для предсказания условий реакций органической химии на основе графов была взята модель графовой сверточной нейронной сети с механизмом внимания на ребрах Edge Attention Graph Convolution Network. Modeling the structure of chemical reactivity from the point of view of the structure of the substances involved has important consequences in all areas of chemistry and biochemistry, from synthesis to understanding metabolic processes. To predict the reaction conditions of organic chemistry based on graphs, we used the model Edge Attention Graph Convolution Network.
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"Innovative cosmetic raw materials and biologically active compounds in cosmetics chemistry." In Chemical technology and engineering. Lviv Polytechnic National University, 2021. http://dx.doi.org/10.23939/cte2021.01.156.

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Cheah, Sin Moh, and Claire Huiting Ng. "Integrating Sustainable Development into Chemical Engineering Curriculum Work Done, Learning Points and Future Directions." In Annual International Conference on Chemistry, Chemical Engineering and Chemical Process. Global Science & Technology Forum (GSTF), 2013. http://dx.doi.org/10.5176/2301-3761_ccecp.01.

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Venkatesu, Pannuru. "Influence of ammonium ionic liquids on structure and stability of myoglobin." In Annual International Conference on Chemistry, Chemical Engineering and Chemical Process. Global Science & Technology Forum (GSTF), 2013. http://dx.doi.org/10.5176/2301-3761_ccecp.03.

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Choudhary, R. B. "An Investigation on Tribo-Chemical Reactions of AF/AW Additive Compounds of Alkyl ThioOctadecenoate Origin." In Annual International Conference on Chemistry, Chemical Engineering and Chemical Process. Global Science & Technology Forum (GSTF), 2013. http://dx.doi.org/10.5176/2301-3761_ccecp.04.

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