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Thematische Bibliographien / Titration

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Auswahl der wissenschaftlichen Literatur zum Thema „Titration“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 14. März 2023

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Zeitschriftenartikel zum Thema "Titration"

1

Fuhrmann, B., und U. Spohn. „A PC-based titrator for flow gradient titrations“. Journal of Automatic Chemistry 15, Nr. 6 (1993): 209–16. http://dx.doi.org/10.1155/s1463924693000276.

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This paper describes a PC (personal computer) based titrator which was developed for gradient flow titrations. Concentration gradients were generated electrolytically or volumetrically in small tubes. Complete titration curves can be recorded on-line and evaluated automatically. The titrator can be used with all liquid flow detectors with low axial dispersion. The titrator was evaluated for the titration of thiosulphate with electrogenerated triiodide and for the titration of ammonia with electrogenerated hypobromite after continuous gas dialytic separation of ammonia from the sample solution.

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FERNANDEZ-MAESTRE, Roberto. „THE IMPORTANCE OF TEACHING TITRATION CURVES IN ANALYTICAL CHEMISTRY“. Periódico Tchê Química 17, Nr. 34 (20.03.2020): 213–19. http://dx.doi.org/10.52571/ptq.v17.n34.2020.230_p34_pgs_213_219.pdf.

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Titration curves are an essential subject of an Analytical Chemistry course. The main objective of calculating titration curves is the selection of an indicator for such titrations. The calculation of titration errors is imperative because they establish if a given indicator can be used for a given titration. This study reviews the available literature on titration curves and calculating their errors. Its purpose is to draw attention to the importance of undergraduate chemistry students having competencies to determine the titration errors rather than skills to build titration curves as the ultimate purpose of these curves is to determine the failure committed when using a given indicator to assess their endpoints. It is shown that the pH and potential calculation at the equivalence point in acid-base and redox titrations, respectively, are not required to choose the titration indicator, one that yields an acceptable error according to the type of application needed. Methods to calculate these errors in the four main types of titrations are presented; those for complexometric and precipitation titrations are simpler than in the literature. Here, it is also demonstrated that calculating points immediately after and before the curve inflection are more critical for this selection in these two types of titrations. Also, it is deducted that complexometric and precipitation curves are not required to select indicators for these titrations. These demonstrations are essential because analytical chemistry teachers may disregard teaching important topics by spending time calculating unnecessary titration curves (complexometric and precipitation titrations) or additional points of titration curves (redox and acid-base titrations) when the calculation of titration errors of these reactions is more critical. Most analytical chemistry textbooks neglect this topic. Undergraduate chemistry programs should focus more on calculating titration errors than on the construction of titration curves.

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Ayoub, Muhammad Haris, Shehryar Ahmad, Zia Ul Hassan, Asad Muhammad Khan, Muhammad Bilal, Amir Waseem und Ahson Jabbar Shaikh. „Understanding non-covalent interactions of graphene oxide toward transition metal surfaces and relation of binding constants with titration end points from dynamic light scattering studies“. Journal of Applied Physics 133, Nr. 2 (14.01.2023): 025303. http://dx.doi.org/10.1063/5.0134267.

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The understanding of non-covalent binding interactions of graphene oxide toward transition metal surfaces (Fe, Co, Ni, and Cu) was observed by ultraviolet–visible absorption spectroscopy, fluorescence emission spectroscopy, hydrodynamic size, and zeta potential studies through titration experiments. These interactions mainly occur through C=C double bonds of graphene oxide. Iron and cobalt nanoparticles interact strongly as compared to nickel and copper nanoparticles. The obtained Stern–Volmer plots are curved indicating that static and dynamic quenching occur simultaneously in these systems. The curves obtained for size titration graphs indicated the saturation end point for these titrations, which were then compared with binding constants obtained from linear Stern–Volmer plots. Interestingly, with lower binding constants, a higher concentration of nanoparticles was required for titration end points. These two complimentary techniques stood well quantitatively toward each other. Upon titrating the nanoparticles with graphene oxide, the zeta potential always lowered close to the value of graphene oxide, indicating that hybrids are more stable than the nanoparticles.

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Feitkenhauer, H., und U. Meyer. „On-line titration of non-ionic surfactants in wastewater treatment plants using a specific electrode“. Water Science and Technology 45, Nr. 4-5 (01.02.2002): 61–68. http://dx.doi.org/10.2166/wst.2002.0552.

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Textile finishing industry wastewater often contains high concentrations of surfactants. Non-ionic surfactants like alcohol ethoxylates are among the most used surfactants and are discharged from batch-processes in widely varying concentrations. The anaerobic biomass and especially methanogenic microorganisms have been shown to be inhibited by surfactants. To protect these microorganisms from irreversible inhibition a measurement of the surfactant concentration is useful for the process control, but most analytical methods are too complicated and expensive for an on-line process control. It was shown that the titration of non-ionic surfactants is possible in the presence of biomass and in wastewater from textile wet processes using the Metrohm NIO-electrode. Titration and sampling were successfully performed with standard equipment. The software used for the process control of a lab-scale anaerobic treatment plant was also used to evaluate the obtained titration curves. This allowed performing the titrations without using a more expensive titrator.

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Gibson, Graham, Alexei A. Neverov und R. S. Brown. „Potentiometric titration of metal ions in methanol“. Canadian Journal of Chemistry 81, Nr. 6 (01.06.2003): 495–504. http://dx.doi.org/10.1139/v03-035.

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The potentiometric titrations of nine lanthanideIII triflates, ZnII and CuII triflate, and the NiII, CoII, MgII, and TiIV perchlorates were obtained in methanol to determine the titration constants (defined as the sspH at which the [OCH3]/[Mx+]t ratios are 0.5 and 1.5) as well as the apparent sspKa values for deprotonation of the metal-bound solvent molecules. The titrations were performed under various conditions with and without added salts as electrolytes, and the variations in the titration constants are discussed. In selected cases (La3+, Zn2+) the titration profiles were analyzed using a complex fitting program to obtain information about the species present in solution.Key words: potentiometric titration, methanol, sspH, metal ion, lanthanides, apparent sspKa.

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Gonzalez, G. G., A. M. Jimenez und A. G. Asuero. „Titration errors in acid-base titrations“. Microchemical Journal 41, Nr. 1 (Februar 1990): 113–20. http://dx.doi.org/10.1016/0026-265x(90)90103-c.

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7

Bodiroga, Milanka, und Jasminka Ognjanovic. „Determination of peracetic acid and hydrogen peroxide in the mixture“. Vojnosanitetski pregled 59, Nr. 3 (2002): 277–79. http://dx.doi.org/10.2298/vsp0203277b.

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Iodometric and permanganometric titrations were used for determination of peracetic acid and hydrogen peroxide (H2O2) in the mixture. Two procedures were described and compared. Titrations could be done in only one vessel, in the same reaction mixture, when iodometric titration of peracetic acid was continued after the permanganometric titration of H2O2, (procedure A). Peracetic acid and H2O2, as oxidizing agents, reacted with potassium iodide in an acid medium, evolving iodine. This reaction was used for the quantitative iodometric determination of total peroxide in procedure B. H2O2 reacted with potassium permanganate in acid medium, but peracetic acid did not react under the same conditions. That made possible the selective permanganometric determination of H2O2 in the presence of peracetic acid. The procedure B was performed in two titration vessels (KV=3.4% for peracetic acid, 0.6% for H2O2). The procedure A for iodometric determination of peracetic acid in one titration vessel after permanganometric titration of H2O2 was recommended (KV=2,5% for peracetic acid, 0,45% for H2O2).

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Bhavya sri Khagga, Srija Ghanukota und Sumakanth Mogili. „Novel titrimetric method for the determination of rosuvastatin in pure form“. World Journal of Biology Pharmacy and Health Sciences 13, Nr. 2 (28.02.2023): 001–4. http://dx.doi.org/10.30574/wjbphs.2023.13.2.0054.

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In this experiment assay of Rosuvastatin was performed by titrimetric method. The titration performed is a complexometric titration. The complexometric titration used is an easy, inexpensive volumetric titration method. This method is based on rection of calcium with a solution of disodium ethylenediaminotetraacetate (EDTA). Complex of calcium and EDTA is formed. Erichrome black Tis used as an indicator in this complexometric titration. At pH 12-13, Erichrome black T changes the color from pink to blue. The appearance blue color is determined to be the endpoint of this experiment. The titrations were carried out in triplicates and the average reading was taken to calculate the percentage assay. The percentage purity was found to be 103.05%

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DiMaria, Michelle, Brian Schultz, Jennifer Falvo, Edward Matthews, Michelle Ward, Jordan Land, Danna Tauber und Suzanne Beck. „0502 Harmony in the Sleep Lab: A Focus on Recognition of Hypoventilation and Direct Feedback Improves Quality of Pediatric Titrations“. Sleep 45, Supplement_1 (25.05.2022): A222. http://dx.doi.org/10.1093/sleep/zsac079.499.

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Abstract Introduction Over 350 pediatric polysomnogram titrations (T-PSGs) are performed each year at the Sleep Laboratory at Children’s Hospital of Philadelphia in three locations by 24 different polysomnography technologists (PSGTs) on a diverse patient population, typically performed as outpatient procedures and occasionally at the bedside as inpatients. PSGTs are responsible for titration of continuous or bilevel positive airway pressure based on flow, work of breathing, arousals, and/or gas exchange. PSGTs have varying degrees of experience; thus, maintaining quality of T-PSGs is challenging. We hypothesized that a quality improvement (QI) approach to reviewing T-PSGs with interdisciplinary education and regular feedback would improve T-PSGs. Our goal was to have >/= 80% of titrations of optimal quality. Methods Each T-PSG record was reviewed by a sleep physician for optimal quality, defined as appropriate signal integrity, titration, and documentation to permit definitive interpretation. Exclusion: RAM cannula use, illness, or external signal interference. Titration QI (T-QI) comments were reviewed by the sleep lab QI team bi-weekly to plan feedback. Improvement interventions for PSGTs included didactic education: lectures, presentations, and cases focusing on recognition of hypoventilation; direct feedback with teaching points by sleep physician and small group sessions with clinical supervisors to review areas for improvement; and communication of specific titration goals. Satisfaction surveys regarding recognition/titration for OSA/hypoventilation, transcutaneous CO2 signal integrity, and documentation were administered to sleep physicians. Results From September 2020-November 2021, PSGT education included: 1 synchronous and 2 asynchronous didactic presentations; 1:1 review of didactics with each night PSGT (n=24); T-QI feedback (2/week); and small group review sessions (4/week). 408 titrations were completed; 42 (10.3%, 2.8/month) were excluded; 366 (89.7%, 24.4/month) were reviewed for T-QI. 54.8% [50,71%] were deemed optimal during the first three months (pre-intervention) vs. 80.1% [63,96%] during the intervention period. QI satisfaction survey showed improvement in 3 of 4 domains. Conclusion Quality of T-PSG is enhanced by QI review of each titration, highlighting teaching points and areas for improvement via direct feedback and small group review. Education and communication among physicians, supervisors and technologists are important to support development which can result in better titrations and satisfaction. Support (If Any) none

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Besenhard, J. O., H. P. Gansmann und H. Meyer. „Bestimmung von Oberflächenoxiden auf Rußen durch potentiometrische Direkttitration in nichtwäßrigen Lösungsmitteln / Determination of Surface Oxides on Carbon Blacks by Direct Potentiometric Titration in Non-Aqueous Solvents“. Zeitschrift für Naturforschung B 45, Nr. 6 (01.06.1990): 857–63. http://dx.doi.org/10.1515/znb-1990-0617.

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An attempt is made to quantitatively determine acidic and basic surface oxides on carbon blacks and also to monitor their acid and base strength distribution by direct potentiometric titrations in non-aqueous media.In contrast to direct titration procedures proposed so far, our method allows to distinguish clearly between several types of acidic surface oxides of different acid strength. This is mainly achieved by improvements of the non-aqueous titration media. The total contents of weakly and strongly acidic and also of basic oxides determined by this very fast method is comparable to results obtained by slow and laborious indirect titrations.

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Dissertationen zum Thema "Titration"

1

Halliday, Colin George. „Aspects of photometric titration“. Thesis, Queen's University Belfast, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329513.

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Fardel, Julien. „Application of thermometric titration methods /“. Sion, 2008. http://doc.rero.ch/record/12817?ln=fr.

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Neville, M. D. „The development of titration membrane electrodes“. Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/47202.

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Butt, Michael David. „Macromolecular thermodynamics studied by titration calorimetry“. Thesis, University of Leicester, 1994. http://hdl.handle.net/2381/34042.

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This thesis is centred on the use of an isothermal titration microcalori-meter which can measure heat changes of the order of a few microcalories. The calorimeter provides a rapid and convenient method, incorporating a thermodynamic analysis, for estimating enthalpic pairwise interaction parameters, hjj, for solute-j in aqueous solution. Estimates of hjj for three solutes; urea, monoethylurea and hexamethylenetetramine are reported. Comparisons with published estimates of hjj show good agreement, and confirm the importance of the new technology in calorimetry. The critical micellar concentrations (cmc's) of a series of l-alkyl-4-alkylpyridinium halide and bisquaternary ammonium bromide surfactants are reported, using q, heat change on injection, as the reporter. The standard enthalpy of micelle formation is also obtained, directly, from titration experiments. An equation is derived for the standard Gibbs energy of micelle formation, for these compounds. Thus, the standard entropy is calculated and the driving force (enthalpy or entropy) for micellisation, of these surfactants, is identified. Injection of small aliquots of fusogenic agents (the dianions of dipicolinic acid and sodium sulphate) into aqueous solutions of dioctadecyldimethyl-ammonium bromide (DOAB) vesicles is endothermic at 50 Celsius. For solutions containing greater than equimolar ratios of DOAB and fusogenic agent, the injection process is effectively athermal. The patterns of enthalpy change are attributed to vesicle-dianion interaction (exothermic) and headgroup dehydration (endothermic). Other effects such as the presence of buffer and the interaction of DOAB with halide monoanions are also discussed. Binding of the substrate, chloramphenicol (CM), to the enzyme, chloramphenicol acetyltransferase (CAT), is exothermic. Calorimetric measurements of a series of injections of CM into CAT, and subsequent analysis, yield the binding constant, number of binding sites per macromolecule (enzyme) and the standard enthalpy of binding for the interaction. These three parameters are presented, together with the standard entropy and standard Gibbs energy of binding.

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Motara, Hasina. „Isothermal titration calorimetric studies of complexation reactions“. Thesis, University of Huddersfield, 2011. http://eprints.hud.ac.uk/id/eprint/10779/.

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The objective of this work has been to study the binding of metal ions to complex ligands expressing two or more metal binding sites, in terms of the thermodynamics of the binding events, and to use this information to contribute to the understanding of both the metal binding processes and the properties of the metal/ligand complexes. Two ligands have formed the basis of the study, one a naturally occurring enzyme and the other a newly synthesised ligand with two distinct binding sites (to form supramolecular complexes). The principle technique used to determine thermodynamic parameters has been isothermal titration calorimetry (ITC). The first system studied involved the enzyme β-lactamase II from Bacillus cereus 569/H/9 (BcII). The binding of zinc (II), cobalt (II) and cadmium (II) was investigated in aqueous solution at pH’s from 5.2 to 7.2. By using three or more buffers at each pH it has been possible to determine not only the binding constants of the metal ions at these pH’s but also the molar enthalpies of binding (and hence molar entropies). In addition, the dissociation of hydrogen ions from the enzyme on metal binding was also observed. In the case of all three metal ions, one metal ion per enzyme appears to bind at low pH and two metal ions at high pH (within the pH 5.20-7.20 range). In the case of zinc and cobalt ions two metal ions seem to bind per mole of enzyme in a cooperative mechanism. In contrast two cadmium ions appear to bind to the active sites of the enzyme non-cooperatively. For all three metal ions, models have been developed to describe the two binding sites and the sources of H+ ions that dissociate on metal ion binding. The second system studied involved the supramolecular synthesised ligand bipy-aza-crown-4. This ligand has two metal binding sites, one at the 2,2-bipyridine and the other at the aza-crown-4. The objective was to compare the way copper (II) binds in acetonitrile solution with the way in which the copper (II) complex with this ligand is crystallised from methanol solution with progressively increased copper (II) concentration, as revealed by single crystal x-ray diffraction. Smaller ligands that represent the two individual complexation regions of the synthesised ligand were also used for comparison. Both ITC and solution spectroscopic measurements were used to compare the binding model that was proposed in methanol solution. It was demonstrated in acetonitrile solution that copper (II) binds to the 2,2-bipyridine site first in a 1:2 (Cu2+:L) ratio, then binds to the aza-crown site in a 1:1 (Cu2+:L) ratio . So it was demonstrated that the overall stoichiometric ratio of copper ion to bipy-aza-crown-4 in the fully formed complex is 3:2 (Cu2+: L). Possibly the main conclusion drawn is that the order in which the binding sites are occupied in acetonitrile solution is different to that in which they are occupied in methanol.

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Ebert, Margaret S. (Margaret Sarah). „Molecular titration by MicroRNAs and target mimic inhibitors“. Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/61886.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2010.
Vita. Cataloged from PDF version of thesis.
Includes bibliographical references.
MicroRNAs (miRNAs) are short, highly conserved non-coding RNA molecules that repress gene expression in a sequence-dependent manner. Each miRNA is predicted to target hundreds of genes, and a majority of protein-coding genes are computationally predicted to be miRNA targets. To test miRNA functions experimentally, we introduced the miRNA "sponge" method, which uses miRNA target mimics to sequester mature miRNAs and thereby create continuous miRNA loss of function in cell lines and transgenic organisms. Sponge RNAs contain complementary binding sites to a miRNA of interest, and are produced from transgenes within cells. As with most miRNA target genes, a sponge's binding sites are specific to the miRNA seed region, which allows them to block a whole family of related miRNAs. This transgenic approach has proven to be a powerful tool to generate miRNA phenotypes in a variety of experimental systems. Bulk measurements on populations of cells have indicated that, although pervasive, repression due to miRNAs is on average quite modest. To assay repression in single cells, we performed quantitative fluorescence microscopy and flow cytometry to monitor a target gene's protein expression in the presence and absence of regulation by miRNA. We found that repression among individual cells varies dramatically. miRNAs establish a threshold level of target mRNA below which protein production is highly repressed and above which expression responds ultra sensitively to target mRNA input until reaching high enough mRNA levels to almost escape repression. We constructed a mathematical model describing molecular titration of target mRNAs by miRNAs. The model predicted, and experiments confirmed, that the ultrasensitive regime could be shifted to higher target mRNA levels by increasing the miRNA concentration or the number of miRNA binding sites in the 3' untranslated region (UTR) of the target mRNA. Thus even a single species of miRNA can act both as a switch to effectively silence gene expression and as a fine-tuner of gene expression. This fits the emerging paradigm in which miRNAs help to confer robustness to biological processes by reinforcing transcriptional programs, attenuating leaky transcripts, and perhaps buffering random fluctuations in transcript copy number.
by Margaret S. Ebert.
Ph.D.

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Relli-Dempsey, Vincent M. T. Relli-Dempsey. „A Thermometric Titration Study of Acetaminophen and Sodium Hypochlorite“. Ohio Dominican University Honors Theses / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=oduhonors152621864170557.

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Rabenstein, Björn. „Monte Carlo methods for simulation of protein folding and titration“. [S.l. : s.n.], 2000. http://www.diss.fu-berlin.de/2000/124/index.html.

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Grünke, Silke. „Reaktionsmechanismen in der Karl-Fischer-Lösung“. [S.l. : s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=957132433.

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Pan, Haobo. „Solubility of calcium phosphates and related oral minerals by solid titration“. Click to view the E-thesis via HKUTO, 2007. http://sunzi.lib.hku.hk/HKUTO/record/B39557558.

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Bücher zum Thema "Titration"

1

Hansen, Lee D., Mark K. Transtrum und Colette F. Quinn. Titration Calorimetry. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78250-8.

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2

L, Mabry Richard, Hrsg. Skin endpoint titration. 2. Aufl. New York: Thieme Medical Publishers, 1994.

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L, Mabry Richard, und American Academy of Otolaryngic Allergy., Hrsg. Skin endpoint titration manual. New York: Thieme Medical Publishers, 1992.

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4

1947-, Grime J. Keith, Hrsg. Analytical solution calorimetry. New York: Wiley, 1985.

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Knapp, George P. Automated oxygen titration and salinity determination. Woods Hole, Mass: Woods Hole Oceanographic Institution, 1990.

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M, Talmud M., Hrsg. Selektivnoe kompleksonometricheskoe titrovanie. Moskva: Nauka, 1993.

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Wieland, G. Water determination by Karl Fischer titration: Theory and applications. Darmstadt: Git Verlag, 1987.

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Selwyn, Lyndsie. Analysis of the chloride ion concentration in aqueous solutions by potentiometric titration. Ottawa, Ont: Canadian Conservation Institute, 2001.

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9

Elkordy, Amal Ali. Applications of calorimetry in a wide context: Differential scanning calorimetry, isothermal titration calorimetry and microcalorimetry. Rijeka, Croatia: Intech, 2013.

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Mwakibete, Hezron Kapaga Ozanne. Electrochemical and isothermal titration calorimetry studies associated with polymer-micelle complexes and surfactant/cyclodextrin inclusion complexes. Salford: University of Salford, 1994.

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Buchteile zum Thema "Titration"

1

Gooch, Jan W. „Titration“. In Encyclopedic Dictionary of Polymers, 752. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11921.

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Arndt, T. „Titration“. In Springer Reference Medizin, 2318. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_3055.

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Arndt, T. „Titration“. In Lexikon der Medizinischen Laboratoriumsdiagnostik, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49054-9_3055-1.

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4

Allemann. „Titration, Grundlagen“. In Analytische Methoden, 41–71. Basel: Birkhäuser Basel, 1988. http://dx.doi.org/10.1007/978-3-0348-5191-6_4.

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Wörfel, P., M. Bitzer, U. Claus, H. Felber, M. Hübel und B. Vollenweider. „Titration, Grundlagen“. In Laborpraxis, 41–71. Basel: Birkhäuser Basel, 1990. http://dx.doi.org/10.1007/978-3-0348-6162-5_4.

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Newall, Fiona. „Protamine Titration“. In Haemostasis, 279–87. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-339-8_21.

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Kahlert, Heike, und Fritz Scholz. „Titration Errors“. In Acid-Base Diagrams, 103–11. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-37902-4_6.

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Crompton, T. R. „Titration Procedures“. In Comprehensive Organometallic Analysis, 149–225. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4615-9498-7_2.

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Nahler, Gerhard. „dose titration study“. In Dictionary of Pharmaceutical Medicine, 55. Vienna: Springer Vienna, 2009. http://dx.doi.org/10.1007/978-3-211-89836-9_413.

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Dancey, Janet, Boris Freidlin und Larry Rubinstein. „Accelerated Titration Designs“. In Statistical Methods for Dose-Finding Experiments, 91–113. Chichester, UK: John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/0470861258.ch4.

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Konferenzberichte zum Thema "Titration"

1

Kaewthai, Ratchanee, Sotarat Thammaboosadee und Supaporn Kiattisin. „Diabetes dose titration identification model“. In 2015 8th Biomedical Engineering International Conference (BMEiCON). IEEE, 2015. http://dx.doi.org/10.1109/bmeicon.2015.7399557.

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2

Wang, Chunlin, Ning Huang, Lina Sun und Guoyi Wen. „A Titration Mechanism Based Congestion Model“. In 2018 IEEE International Conference on Software Quality, Reliability and Security Companion (QRS-C). IEEE, 2018. http://dx.doi.org/10.1109/qrs-c.2018.00089.

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3

Frede, T. Aljoscha, Stefan Hoving, Konrad E. R. Boettcher, Ines Aubel und Norbert Kockmann. „Microcontroller-based Titration for Remote Lab“. In 2022 IEEE German Education Conference (GeCon). IEEE, 2022. http://dx.doi.org/10.1109/gecon55699.2022.9942767.

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4

Verner, Igor M., und Leonid B. Revzin. „Towards Automation of Manual Operations in a High School Chemistry Laboratory“. In ASME 2008 9th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2008. http://dx.doi.org/10.1115/esda2008-59037.

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Annotation:

This paper proposes a learning environment in which manual operations of school chemistry laboratory experiments, such as titration and aliquoting, are automated by means of computer controlled devices. The educational study focuses on characteristics of learning in the automated laboratory environment. Pilot teaching indicated that using automation devices significantly reduces the performance time of titration laboratory work. The students also noted that automated titration experiments are more simple and accurate. Therefore, automation of manual operations in laboratory practice has been found to provide a very positive learning environment.

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5

Chamberlain, Roger D., Chris Edmiston und Don Williams. „Automated Titration in a Recirculating Water System“. In 2018 International Workshop on Cyber-physical Systems for Smart Water Networks (CySWater). IEEE, 2018. http://dx.doi.org/10.1109/cyswater.2018.00010.

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6

Gullaian, Martin, und John Lane. „Titration Curve Estimation for Adaptive pH Control“. In 1990 American Control Conference. IEEE, 1990. http://dx.doi.org/10.23919/acc.1990.4790971.

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7

Vandeput, S., F. Beckers, B. Verheyden, A. E. Aubert und S. Van Huffel. „Application of numerical noise titration during autonomic blockade“. In 2007 34th Annual Computers in Cardiology Conference. IEEE, 2007. http://dx.doi.org/10.1109/cic.2007.4745538.

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8

Kawai, Kentaro, Masaru Fujii und Shuichi Shoji. „Pricise Titration Microfluidic System using Sub-Picoliter Droplet Injection“. In 2009 IEEE 22nd International Conference on Micro Electro Mechanical Systems. MEMS 2009. IEEE, 2009. http://dx.doi.org/10.1109/memsys.2009.4805433.

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9

Silu Zhang, Pengyuan Zang, Yuchen Liang und Walter Hu. „Determination of protein titration curves using Si Nanograting FETs“. In 2014 IEEE 14th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2014. http://dx.doi.org/10.1109/nano.2014.6968097.

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10

Isnardi, E., F. Bertolino und G. Prest. „Do the CPAP auto titration systems (APAP) require calibration?“ In Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa959.

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Berichte der Organisationen zum Thema "Titration"

1

Hansen, Lance D., David D. Ringelberg, Deborah R. Felt und Jeffrey D. Davis. Base-Induced 2,4,6-Trinitrotoluene Transformation, Titration Studies. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada396037.

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2

Lee, Michael S., Freddie R. Salsbury, Brooks III Jr und Charles L. Constant-pH Molecular Dynamics using Continuous Titration Coordinates. Fort Belvoir, VA: Defense Technical Information Center, August 2004. http://dx.doi.org/10.21236/ada426290.

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3

Rogers, Kayron, Benjamin Roach, Jenn Parikh, Haley Wightman, Ralph Ilgner, Marc Chattin, Cole Hexel und Joseph {Joe} Giaquinto. New Capability at ORNL: High Precision Uranium Titration. Office of Scientific and Technical Information (OSTI), Juli 2021. http://dx.doi.org/10.2172/1811394.

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4

Cureton, LaShonda T., George Fountzoulas und John J. La Scala. Molecular Weight Measurement of Biobased Furan Polyamides via Non-Aqueous Potentiometric Titration. Fort Belvoir, VA: Defense Technical Information Center, Juni 2013. http://dx.doi.org/10.21236/ada586113.

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5

Christensen, Earl, Jack Ferrell, Mariefel V. Olarte, Asanga B. Padmaperuma und Teresa Lemmon. Acid Number Determination of Pyrolysis Bio-oils using Potentiometric Titration: Laboratory Analytical Procedure (LAP). Office of Scientific and Technical Information (OSTI), März 2016. http://dx.doi.org/10.2172/1241091.

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6

Sopok, Samuel. Determination of Trivalent Chromium in Chromium Plating Solutions Using a Redox Titration and Indicator. Fort Belvoir, VA: Defense Technical Information Center, Mai 1992. http://dx.doi.org/10.21236/ada252857.

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7

Sopok, Samuel. Determination of Chromic Acid in Chromium Plating Solutions Using a Redox Titration and Indicator. Fort Belvoir, VA: Defense Technical Information Center, August 1989. http://dx.doi.org/10.21236/ada220641.

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8

Taylor-Pashow, Kathryn M. L., und Daniel H. Jones. Non-Aqueous Titration Method for Determining Suppressor Concentration in the MCU Next Generation Solvent (NGS). Office of Scientific and Technical Information (OSTI), Oktober 2017. http://dx.doi.org/10.2172/1404909.

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9

Black, Stuart, Jack Ferrell, Mariefel V. Olarte und Asanga B. Padmaperuma. Determination of Carbonyls in Pyrolysis Bio-oils by Potentiometric Titration. Faix Method. Laboratory Analytical Procedure (LAP). Office of Scientific and Technical Information (OSTI), März 2016. http://dx.doi.org/10.2172/1241099.

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10

Sopok, Samuel. Determination of Nickel, Nickel Chloride Hexahydrate and Boric Acid in Nickel Sulfamate Plating Solutions by Titration. Fort Belvoir, VA: Defense Technical Information Center, Juni 1991. http://dx.doi.org/10.21236/ada420005.

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