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Sample records for automated potentiometric titrations

  1. Semi-automated potentiometric titration method for uranium characterization.

    Science.gov (United States)

    Cristiano, B F G; Delgado, J U; da Silva, J W S; de Barros, P D; de Araújo, R M S; Lopes, R T

    2012-07-01

    The manual version of the potentiometric titration method has been used for certification and characterization of uranium compounds. In order to reduce the analysis time and the influence of the analyst, a semi-automatic version of the method was developed in the Brazilian Nuclear Energy Commission. The method was applied with traceability assured by using a potassium dichromate primary standard. The combined standard uncertainty in determining the total concentration of uranium was around 0.01%, which is suitable for uranium characterization. PMID:22154105

  2. Semi-automated potentiometric titration method for uranium characterization

    International Nuclear Information System (INIS)

    The manual version of the potentiometric titration method has been used for certification and characterization of uranium compounds. In order to reduce the analysis time and the influence of the analyst, a semi-automatic version of the method was developed in the Brazilian Nuclear Energy Commission. The method was applied with traceability assured by using a potassium dichromate primary standard. The combined standard uncertainty in determining the total concentration of uranium was around 0.01%, which is suitable for uranium characterization. - Highlights: ► We developed a semi-automatic version of potentiometric titration method. ► The method is used for certification and characterization of uranium compounds. ► The traceability of the method was assured by a K2Cr2O7 primary standard. ► The results of U3O8 reference material analyzed was consistent with certified value. ► The uncertainty obtained, near 0.01%, is useful for characterization purposes.

  3. Semi-automated potentiometric titration method for uranium characterization

    Energy Technology Data Exchange (ETDEWEB)

    Cristiano, B.F.G., E-mail: barbara@ird.gov.br [Comissao Nacional de Energia Nuclear (CNEN), Instituto de Radioprotecao e Dosimetria (IRD), Avenida Salvador Allende s/n Recreio dos Bandeirantes, PO Box 37750, Rio de Janeiro, 22780-160 RJ (Brazil); Delgado, J.U.; Silva, J.W.S. da; Barros, P.D. de; Araujo, R.M.S. de [Comissao Nacional de Energia Nuclear (CNEN), Instituto de Radioprotecao e Dosimetria (IRD), Avenida Salvador Allende s/n Recreio dos Bandeirantes, PO Box 37750, Rio de Janeiro, 22780-160 RJ (Brazil); Lopes, R.T. [Programa de Engenharia Nuclear (PEN/COPPE), Universidade Federal do Rio de Janeiro (UFRJ), Ilha do Fundao, PO Box 68509, Rio de Janeiro, 21945-970 RJ (Brazil)

    2012-07-15

    The manual version of the potentiometric titration method has been used for certification and characterization of uranium compounds. In order to reduce the analysis time and the influence of the analyst, a semi-automatic version of the method was developed in the Brazilian Nuclear Energy Commission. The method was applied with traceability assured by using a potassium dichromate primary standard. The combined standard uncertainty in determining the total concentration of uranium was around 0.01%, which is suitable for uranium characterization. - Highlights: Black-Right-Pointing-Pointer We developed a semi-automatic version of potentiometric titration method. Black-Right-Pointing-Pointer The method is used for certification and characterization of uranium compounds. Black-Right-Pointing-Pointer The traceability of the method was assured by a K{sub 2}Cr{sub 2}O{sub 7} primary standard. Black-Right-Pointing-Pointer The results of U{sub 3}O{sub 8} reference material analyzed was consistent with certified value. Black-Right-Pointing-Pointer The uncertainty obtained, near 0.01%, is useful for characterization purposes.

  4. Implementation of the automated potentiometric titration method for total U at the CNEN Safeguard Laboratory, Brazil

    International Nuclear Information System (INIS)

    Brazilian nuclear facilities, in accordance with the regulation CNEN-NN-2.02, must have available measurement systems which allow to determine their nuclear material inventories. For the evaluation and the follow up the performance of the involved laboratories in those measurement systems, the accomplishment of interlaboratory comparison programmes becomes fundamental. Therefore, the implementation of the potentiometric titration viewing the characterization of uranium samples, represents an reference element for the Brazilian programs

  5. A generalized approach for the calculation and automation of potentiometric titrations Part 1. Acid-Base Titrations

    NARCIS (Netherlands)

    Stur, J.; Bos, M.; Linden, van der W.E.

    1984-01-01

    Fast and accurate calculation procedures for pH and redox potentials are required for optimum control of automatic titrations. The procedure suggested is based on a three-dimensional titration curve V = f(pH, redox potential). All possible interactions between species in the solution, e.g., changes

  6. Determination of total acidity index in bioethanol by automated potentiometric titration; Determinacao do indice de acidez total em bioetanol por titulacao potenciometrica automatizada

    Energy Technology Data Exchange (ETDEWEB)

    Sobral, Sidney Pereira; Ribeiro, Carla de Matos; Fraga, Isabel Cristina Serta; Goncalves, Mary Ane [Instituto Nacional de Metrologia, Normalizacao e Qualidade Industrial (DIMCI/INMETRO), Duque de Caxias, RJ (Brazil). Diretoria de Metrologia Cientifica e Industrial], E-mail: spsobral@inmetro.gov.br

    2009-07-01

    This paper determines the total acidity index of bioethanol by volumetric titration with potentiometric detection. Also, viewing the optimization of the method, studies are exhibited related to the repeatable, besides the comparison with the colorimetric method with the objective to contribute to the certification of bioethanol reference materials.

  7. Implementation and assessment of a computerized potentiometric titration

    International Nuclear Information System (INIS)

    Potentiometric titrations still have a great importance in the work of chemical analysis laboratories of different nature, as well as in the Chemistry programs or related to this discipline. At the same time, such titrations have been frequently criticized as tedious and arduous. At our laboratories, potentiometric titrations are important to determine the performance of several radiochemical separations and as a complement to the nuclear techniques in some analysis. Due to the automatic potentiometric titrations high-cost, some authors have proposed some relatively low-cost alternatives that may be built or implemented in research, services or instruction analytical laboratories. This work describes a controlled system by computer, developed and used at the Chemical Department laboratories of the General Direction of Promotion and Technological Development of IPEN

  8. Simple home-made sensors for potentiometric titrations

    International Nuclear Information System (INIS)

    A sensor for potentiometric titrations was prepared by coating a spectroscopic graphite rod with a solution of poly(vinyl chloride) and dioctyphthalate in tetrahydrofuran. The reference electrode was an Ag/AgCl single-junction electrode. The sensor was used in precipitation, acid-base, compleximetric, and redox titrations. Preparation of the coated-graphite sensor is simple and rapid. Moreover, it is quite inexpensive. A limitation is its applicability in aqueous media only, because organic solvents will dissolve the membrane. Various uncoated types of graphite have also been investigated as sensors, particularly in two applications of interest in the analysis of propellants: the titration of nitroform and perchlorate. Obviously, these sensors can be used also in nonaqueous, or partially nonaqueous media. These sensors may also find use in the potentiometric titration of fluoride vs La(III) or Th

  9. SURFACE PROPERTIES AND MODELLING POTENTIOMETRIC TITRATION OF AQUEOUS ILLITE SUSPENSIONS

    OpenAIRE

    Kriaa, A.; Hamdi, N.; Srasra, E.

    2008-01-01

    Potentiometric titration behaviour of complex illitic clay minerals, provided from different origins (two Tunisian illite samples and an American illite sample), were investigated and interpreted according to surface complexation theory. In the present investigation, the focus was on the surface charge characteristics. Proton surface charge can be calculated by subtracting supernatant titration curves from those of illite suspension at ambient temperature and aerated medium. The points of zer...

  10. Natural Monocrystalline Pyrite as Sensor for Potentiometric Redox Titrations. Part I. Titrations with Permanganate

    OpenAIRE

    Vukanovic, B. V.; Mihajlovic, R. P.; Antonijevic, M. M.

    2002-01-01

    Results obtained in potentiometric titrations of Fe(II), Mn(II), Fe(CN)64-, C2O42- and As(III) with standard potassium permanganate solution, are presented. The titration end point (TEP) was detected with a universal electrode whose sensor is natural crystalline pyrite. The titrations of As(III) were carried out in HCl (1.2 M) and H2SO4 solutions (0.1- 4.5 M), whereas oxalate was determined in H2SO4 (0.1-4.5 M). Iron(II) and hexacyanoferrate(II) were titrated in H2SO4 and also in H3PO4 soluti...

  11. Characterization of Native and Modified Starches by Potentiometric Titration

    OpenAIRE

    Diana Soto; Jose Urdaneta; Kelly Pernia

    2014-01-01

    The use of potentiometric titration for the analysis and characterization of native and modified starches is highlighted. The polyelectrolytic behavior of oxidized starches (thermal and thermal-chemical oxidation), a graft copolymer of itaconic acid (IA) onto starch, and starch esters (mono- and diester itaconate) was compared with the behavior of native starch, the homopolymer, and the acid employed as a graft monomer and substituent. Starch esters showed higher percentages of acidity, follo...

  12. Characterization of Native and Modified Starches by Potentiometric Titration

    Directory of Open Access Journals (Sweden)

    Diana Soto

    2014-01-01

    Full Text Available The use of potentiometric titration for the analysis and characterization of native and modified starches is highlighted. The polyelectrolytic behavior of oxidized starches (thermal and thermal-chemical oxidation, a graft copolymer of itaconic acid (IA onto starch, and starch esters (mono- and diester itaconate was compared with the behavior of native starch, the homopolymer, and the acid employed as a graft monomer and substituent. Starch esters showed higher percentages of acidity, followed by graft copolymer of itaconic acid and finally oxidized starches. Analytical techniques and synthesis of modified starches were also described.

  13. Implementation of the automated potentiometric titration method for total U at the CNEN Safeguard Laboratory, Brazil; Implementacao do metodo de titulacao potenciometrica automatizado para U total no Laboratorio de Salvaguardas da CNEN, Brasil

    Energy Technology Data Exchange (ETDEWEB)

    Cristiano, Barbara F.G.; Delgado, Jose U.; Araujo, Radier M.S. de; Silva, Jose W.S. da; Barros, Pedro D. de, E-mail: barbara@ird.gov.b [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2009-07-01

    Brazilian nuclear facilities, in accordance with the regulation CNEN-NN-2.02, must have available measurement systems which allow to determine their nuclear material inventories. For the evaluation and the follow up the performance of the involved laboratories in those measurement systems, the accomplishment of interlaboratory comparison programmes becomes fundamental. Therefore, the implementation of the potentiometric titration viewing the characterization of uranium samples, represents an reference element for the Brazilian programs

  14. Natural Monocrystalline Pyrite as Sensor for Potentiometric Redox Titrations. Part I. Titrations with Permanganate

    Directory of Open Access Journals (Sweden)

    B. V. Vukanovic

    2002-04-01

    Full Text Available Results obtained in potentiometric titrations of Fe(II, Mn(II, Fe(CN64-, C2O42- and As(III with standard potassium permanganate solution, are presented. The titration end point (TEP was detected with a universal electrode whose sensor is natural crystalline pyrite. The titrations of As(III were carried out in HCl (1.2 M and H2SO4 solutions (0.1- 4.5 M, whereas oxalate was determined in H2SO4 (0.1-4.5 M. Iron(II and hexacyanoferrate(II were titrated in H2SO4 and also in H3PO4 solutions (0.1-4.5 M. The titrations of Mn(II were performed in H2P2O72- media at pH 4.0, 5.0, 6.0 and 7.0. The results obtained by using the pyrite electrode were compared with those obtained by the application of a Pt-electrode, and good agreement, reproducibility and accuracy were obtained. The potentials in the course of the titration and at the end-point (TEP are rapidly established. The potential changes at the TEP ranged from 90 to 330 mV/0.1 mL, depending on the titrated system. The highest changes were observed in titrations of Fe(II in H3PO4 (240-330 mV/0.1 mL. Reversed titrations were also performed and accurate and reproducible results were obtained.

  15. Comparison of methods for accurate end-point detection of potentiometric titrations

    Science.gov (United States)

    Villela, R. L. A.; Borges, P. P.; Vyskočil, L.

    2015-01-01

    Detection of the end point in potentiometric titrations has wide application on experiments that demand very low measurement uncertainties mainly for certifying reference materials. Simulations of experimental coulometric titration data and consequential error analysis of the end-point values were conducted using a programming code. These simulations revealed that the Levenberg-Marquardt method is in general more accurate than the traditional second derivative technique used currently as end-point detection for potentiometric titrations. Performance of the methods will be compared and presented in this paper.

  16. Comparative Study of the Total Acidity Determination in Wine by Potentiometric and Volumetric Titration

    OpenAIRE

    Budić-Leto, Irena; Mešin, Nela; Gajdoš Kljusurić, Jasenka; Pezo, Ivan; Bralić, Marija

    2009-01-01

    Total acidity was determined in thirty-seven samples of Croatian red, white and rosé wines by potentiometric titration. In order to find the effect of the corresponding rate of the automatic titrant added, several procedures were employed. For different rates of titration, the aberrances were found from 0.1 to 0.4 g L–1 for some wines. The value of the total acid content in wine determined by the automatic potentiometric titration method was compared to that obtained by the conventional volum...

  17. Further investigation on the degree of deacetylation of chitosan determined by potentiometric titration.

    OpenAIRE

    Kamal Sweidan; Abdel-Motalleb Jaberb; Nawzat Al-jbour; Rana Obaidat; Mayyas Al-Remawi; Adnan Badwan

    2011-01-01

    The degree of deacetylation (DDA) of various low molecular weight chitosan (LMWC) species as the hydrochloride and free base (amine form) was determined by direct and back potentiometric titration,respectively. The DDA values obtained for the chitosan hydrochloride by direct titration were greater than 93% for all oligomers tested (Molecular weight (Mwt) between about 1.3 to 30.0 kDa). However, the DDA values obtained for chitosan amine oligomers using back titration were significantly lower,...

  18. Determination of Sulfides in FCC Gasoline by Using the Potentiometric Titration of Lead Tetraacetate

    Institute of Scientific and Technical Information of China (English)

    罗立文; 夏道宏

    2004-01-01

    Compared with conventional method of violet spectrum, determination of the content of sulfides in fluid catalytic cracking (FCC) gasoline by using the potentiometric titration of lead tetraacetate has some advantages such as clear potentiometric abrupt change at the stoichiometric point, stable potentiometric value, exact and credible results, and simple operation. The content of sulfides in FCC gasoline of Shenghua refinery is 0.136% by this method. The standard deviation about this method is less than 0.01% and the relative standard deviation is less than 2.42%.

  19. Method for linearizing the potentiometric curves of precipitation titration in nonaqueous and aqueous-organic solutions

    International Nuclear Information System (INIS)

    The method for linearizing the potentiometric curves of precipitation titration is studied for its application in the determination of halide ions (Cl-, Br-, I-) in dimethylacetamide, dimethylformamide, in which titration is complicated by additional equilibrium processes. It is found that the method of linearization permits the determination of the titrant volume at the end point of titration to high accuracy in the case of titration curves without a potential jump in the proximity of the equivalent point (5 x 10-5 M). 3 refs., 2 figs., 3 tabs

  20. Data processing for potentiometric precipitation titration of mixtures of isovalent ions by linear regression analysis

    International Nuclear Information System (INIS)

    A method for the computer processing of the curves of potentiometric differential titration using the precipitation reactions is developed. This method is based on transformation of the titration curve into a line of multiphase regression, whose parameters determine the equivalence points and the solubility products of the formed precipitates. The computational algorithm is tested using experimental curves for the titration of solutions containing Hg(2) and Cd(2) by the solution of sodium diethyldithiocarbamate. The random errors (RSD) for the titration of 1x10-4M solutions are in the range of 3-6%. 7 refs.; 2 figs.; 1 tab

  1. Comparative Study of the Total Acidity Determination in Wine by Potentiometric and Volumetric Titration

    Directory of Open Access Journals (Sweden)

    Irena Budić-leto

    2009-03-01

    Full Text Available Total acidity was determined in thirty-seven samples of Croatian red, white and rosé wines by potentiometric titration. In order to find the effect of the corresponding rate of the automatic titrant added, several procedures were employed. For different rates of titration, the aberrances were found from 0.1 to 0.4 g L–1 for some wines. The value of the total acid content in wine determined by the automatic potentiometric titration method was compared to that obtained by the conventional volumetric titration method. The ANOVA and cluster analysis (CA were applied to detect possible resemblance. The results of total acidity depended on the methods used. However, a good correlation between the results by these methods was found.

  2. A novel approach for high precision rapid potentiometric titrations: Application to hydrazine assay

    Science.gov (United States)

    Sahoo, P.; Malathi, N.; Ananthanarayanan, R.; Praveen, K.; Murali, N.

    2011-11-01

    We propose a high precision rapid personal computer (PC) based potentiometric titration technique using a specially designed mini-cell to carry out redox titrations for assay of chemicals in quality control laboratories attached to industrial, R&D, and nuclear establishments. Using this technique a few microlitre of sample (50-100 μl) in a total volume of ˜2 ml solution can be titrated and the waste generated after titration is extremely low comparing to that obtained from the conventional titration technique. The entire titration including online data acquisition followed by immediate offline analysis of data to get information about concentration of unknown sample is completed within a couple of minutes (about 2 min). This facility has been created using a new class of sensors, viz., pulsating sensors developed in-house. The basic concept in designing such instrument and the salient features of the titration device are presented in this paper. The performance of the titration facility was examined by conducting some of the high resolution redox titrations using dilute solutions--hydrazine against KIO3 in HCl medium, Fe(II) against Ce(IV) and uranium using Davies-Gray method. The precision of titrations using this innovative approach lies between 0.048% and 1.0% relative standard deviation in different redox titrations. With the evolution of this rapid PC based titrator it was possible to develop a simple but high precision potentiometric titration technique for quick determination of hydrazine in nuclear fuel dissolver solution in the context of reprocessing of spent nuclear fuel in fast breeder reactors.

  3. Statistical evaluation of an interlaboratory comparison for the determination of uranium by potentiometric titration

    International Nuclear Information System (INIS)

    Upon request of the ESARDA working group 'Low enriched uranium conversion - and fuel fabrication plants' an interlaboratory comparison was organized, to assess the precision and accuracy concerning the determination of uranium by the potentiometric titration method. This report presents the results of a statistical evaluation on the data of the first phase of this exercise. (author). 9 refs.; 5 figs.; 24 tabs

  4. A study on dissociation and complexation of fuivic acid from weathered coal using potentiometric titration

    International Nuclear Information System (INIS)

    The dissociation and complexation of fulvic acid from weathered coal (from Gong Xian, Henan Province) are studied by means of potentiometric titrations. The effects of salt concentration and functional group heterogeneity on the apparent dissociation constants are characterized. Some characteristics of the binding of the ions Cu(II), Th(IV) and La(III) on this fulvic acid are determined

  5. Sequential injection titration of chloride in milk with potentiometric detection

    OpenAIRE

    Lima, M.J. Reis; Fernandes, Sílvia M. V.; Rangel, António O.S.S.

    2004-01-01

    In this work, a sequential injection system for the pseudo-titration of chloride in milk is described. Milk was directly aspirated into the system and sandwiched between two silver nitrate plugs (titrant). The aspirated zones were then propelled to the detector (Ag2S/Ag tubular electrode), where the depletion in the titrant silver concentration (due to the formation of a AgCl precipitate) was monitored. The results obtained by the developed sequential injection titration method were ...

  6. Potentiometric titration of excess cadmium in cadmium selenide

    International Nuclear Information System (INIS)

    A simple and rapid potentiometric technique for determining excess cadmium in CdSe has been developed. Reaction with AgNO3 is used for sample treatment. Silver, formed in the AgNO3 reaction with excess Cd is determined with the help of KI. When using the given method of analysis the relative standard deviation is equal to 0.08-0.21. The real detection limit of excess cadmium is 9x10-7 g

  7. Linear regression analysis of potentiometric titration data for asymmetric redox reactions

    International Nuclear Information System (INIS)

    A statistical method of processing the curves of potentiometric titration for homogeneous asymmetric redox reactions has been suggested. The method was tested using a model titrimetric system Mohr's salt-K2Cr2O7 and was employed for Te determination in an individual solution, semiconductor alloy and CdTe ceramics. Random error of the equivalence point evaluation by the data of a specific titration of 0.1-0.01 M solutions does not exceed 0.3% in case of titration of 0.001 M solutions it increases up to 1.2%. The value of sr varies from 0.0006 to 0.007

  8. Semi-automatic version of the potentiometric titration method for characterization of uranium compounds

    International Nuclear Information System (INIS)

    The potentiometric titration method was used for characterization of uranium compounds to be applied in intercomparison programs. The method is applied with traceability assured using a potassium dichromate primary standard. A semi-automatic version was developed to reduce the analysis time and the operator variation. The standard uncertainty in determining the total concentration of uranium was around 0.01%, which is suitable for uranium characterization and compatible with those obtained by manual techniques. - Highlights: ► A semi-automatic potentiometric titration method was developed for U charaterization. ► K2Cr2O7 was the only certified reference material used. ► Values obtained for U3O8 samples were consistent with certified. ► Uncertainty of 0.01% was useful for characterization and intercomparison program.

  9. Semi-automatic version of the potentiometric titration method for characterization of uranium compounds.

    Science.gov (United States)

    Cristiano, Bárbara F G; Delgado, José Ubiratan; da Silva, José Wanderley S; de Barros, Pedro D; de Araújo, Radier M S; Dias, Fábio C; Lopes, Ricardo T

    2012-09-01

    The potentiometric titration method was used for characterization of uranium compounds to be applied in intercomparison programs. The method is applied with traceability assured using a potassium dichromate primary standard. A semi-automatic version was developed to reduce the analysis time and the operator variation. The standard uncertainty in determining the total concentration of uranium was around 0.01%, which is suitable for uranium characterization and compatible with those obtained by manual techniques. PMID:22406220

  10. Interlaboratory comparison exercise for the determination of uranium by potentiometric titration (first phase)

    International Nuclear Information System (INIS)

    Upon request of the Esarda working group on low-enriched uranium conversion and fuel fabrication plants an interlaboratory comparison was organized, to assess the precision and accuracy concerning the determination of uranium by the potentiometric titration method. This report presents the results of the first phase of this exercise (pure uranyl-nitrate solutions). The solutions used in this intercomparison have been certified for their uranium content by the CBNM, Geel. Comparison of the laboratory results with the certified values shows excellent, good and fairly good agreement for many of the participating laboratories. 10 tabs., 5 figs., 10 refs

  11. Method of semi-automatic high precision potentiometric titration for characterization of uranium compounds

    International Nuclear Information System (INIS)

    The method of high precision potentiometric titration is widely used in the certification and characterization of uranium compounds. In order to reduce the analysis and diminish the influence if the annalist, a semi-automatic version of the method was developed at the safeguards laboratory of the CNEN-RJ, Brazil. The method was applied with traceability guaranteed by use of primary standard of potassium dichromate. The standard uncertainty combined in the determination of concentration of total uranium was of the order of 0.01%, which is better related to traditionally methods used by the nuclear installations which is of the order of 0.1%

  12. The investigation of iron oxyhydroxides precipitation process by potentiometric titration method

    OpenAIRE

    Abuzarova, Kamila

    2013-01-01

    It was investigated the iron oxyhydroxide precipitation process by potentiometric titration method of such systems: Fe₂(SO₄)₃-X-H₂O, Fe(NO₃)₃-X-H₂O, FeCl₃-XH₂O, where X – NH₄OH, Na₂CO₃, CO(NH₂)₂. It was determined the optimum ratio (equivalent) between the amount of a precipitator and an initial salt solution on the base of the experimental data. It was assumed previous conditions of carrying out the precipitation process for this ratio.

  13. Comparing characterization of functionalized multi-walled carbon nanotubes by potentiometric proton titration, NEXAFS, and XPS

    Institute of Scientific and Technical Information of China (English)

    Zhiteng Zhang; Lisa Pfefferle; Gary L. Haller

    2014-01-01

    Since the discovery of carbon nanotubes (CNT), this material has been recognized as an attractive catalyst support. CNT must be functionalized before use as a catalyst support and typically this involves oxidation. However, the functional group distribution on the CNT is very complex mixture of groups and varies with oxidation agent used. Here a simple acid-base titration is introduced to characterize the oxygen functionalized CNT. By comparing characterization with near-edge X-ray absorption fine structure (NEXAFS) and X-ray photoelectron spectroscopy (XPS) for both at the C and O K-edges, it can be demonstrated that potentiometric proton titration can be a fast and quan-titative analysis for Brönsted acid functional groups on CNT.

  14. Surface Complexation Modeling in Variable Charge Soils: Charge Characterization by Potentiometric Titration

    Directory of Open Access Journals (Sweden)

    Giuliano Marchi

    2015-10-01

    Full Text Available ABSTRACT Intrinsic equilibrium constants of 17 representative Brazilian Oxisols were estimated from potentiometric titration measuring the adsorption of H+ and OH− on amphoteric surfaces in suspensions of varying ionic strength. Equilibrium constants were fitted to two surface complexation models: diffuse layer and constant capacitance. The former was fitted by calculating total site concentration from curve fitting estimates and pH-extrapolation of the intrinsic equilibrium constants to the PZNPC (hand calculation, considering one and two reactive sites, and by the FITEQL software. The latter was fitted only by FITEQL, with one reactive site. Soil chemical and physical properties were correlated to the intrinsic equilibrium constants. Both surface complexation models satisfactorily fit our experimental data, but for results at low ionic strength, optimization did not converge in FITEQL. Data were incorporated in Visual MINTEQ and they provide a modeling system that can predict protonation-dissociation reactions in the soil surface under changing environmental conditions.

  15. Determination of vanadium(V) by direct automatic potentiometric titration with EDTA using a chemically modified electrode as a potentiometric sensor.

    Science.gov (United States)

    Quintar, S E; Santagata, J P; Cortinez, V A

    2005-10-15

    A chemically modified electrode (CME) was prepared and studied as a potentiometric sensor for the end-point detection in the automatic titration of vanadium(V) with EDTA. The CME was constructed with a paste prepared by mixing spectral-grade graphite powder, Nujol oil and N-2-naphthoyl-N-p-tolylhydroxamic acid (NTHA). Buffer systems, pH effects and the concentration range were studied. Interference ions were separated by applying a liquid-liquid extraction procedure. The CME did not require any special conditioning before using. The electrode was constructed with very inexpensive materials and was easily made. It could be continuously used, at least two months without removing the paste. Automatic potentiometric titration curves were obtained for V(V) within 5 x 10(-5) to 2 x 10(-3)M with acceptable accuracy and precision. The developed method was applied to V(V) determination in alloys for hip prosthesis. PMID:18970248

  16. Determination of quaternary ammonium compounds by potentiometric titration with an ionic surfactant electrode: single-laboratory validation.

    Science.gov (United States)

    Price, Randi; Wan, Ping

    2010-01-01

    A potentiometric titration for determining the quaternary ammonium compounds (QAC) commonly found in antimicrobial products was validated by a single laboratory. Traditionally, QACs were determined by using a biphasic (chloroform and water) manual titration procedure. Because of safety considerations regarding chloroform, as well as the subjectivity of color indicator-based manual titration determinations, an automatic potentiometric titration procedure was tested with quaternary nitrogen product formulations. By using the Metrohm Titrando system coupled with an ionic surfactant electrode and an Ag/AgCl reference electrode, titrations were performed with various QAC-containing formulation products/matrixes; a standard sodium lauryl sulfate solution was used as the titrant. Results for the products tested are sufficiently reproducible and accurate for the purpose of regulatory product enforcement. The robustness of the method was measured by varying pH levels, as well as by comparing buffered versus unbuffered titration systems. A quantitation range of 1-1000 ppm quaternary nitrogen was established. Eight commercially available antimicrobial products covering a variety of matrixes were assayed; the results obtained were comparable to those obtained by the manual titration method. Recoveries of 94 to 104% were obtained for spiked samples. PMID:21140668

  17. Pitfalls and Uncertainties of Using Potentiometric Titration for Estimation of Plant Roots Surface Charge and Acid-Base Properties

    OpenAIRE

    Grzegorz Jozefaciuk; Alicja Szatanik-Kloc; Malgorzata Lukowska; Justyna Szerement

    2014-01-01

    Amount and properties of roots surface charge are important for nutrient uptake and balance in plants. Roots surface charge markedly varies at different rizosphere conditions (particularly pH and ionic strength), which can markedly alter during vegetation season. Among recently available measuring methods, surface charge-pH dependence of roots (as well as other biological objects) is most easily evaluated by potentiometric titration. Use of this method is also easy at d...

  18. Evaluation of the performance of a metrohm titrator titrando-836 in potentiometric analysis of uranium for safeguards purposes

    International Nuclear Information System (INIS)

    To achieve the requirements of the Brazilian State System of Accounting for and Control of Nuclear Materials - SSAC the Safeguards Laboratory of Brazilian Nuclear Energy Commission, LASAL, has been applying the 'Davies and Gray/NBL' method for Potentiometric determination of total uranium concentration in several forms of nuclear materials since 1984. To improve the accuracy and the repeatability the method uses as titrant, standard reference potassium dichromate NIST SRM 136e and the results are also corrected for bias with NBL CRM 112A uranium metal assay standard. This work describes the assays performed for validation of a Metrohm 836 potentiometric titrator acquired by LASAL in order to improve the analytical methodology of the laboratory. The titrator is attached to a Pt:Rh (90:10) as indicator electrode and a mercurous sulfate as the reference electrode. The evaluation of accuracy and repeatability were made by comparison, the results provided by the titrator with the certified value of standards and also by the participation in round robin program sponsored by New Brunswick Laboratory - NBL. The validation was done by a comparison of the performance between the Metrohm 836 and a Mettler - DL67 titrator which has currently been used by the laboratory. It included evaluation of the results of both equipment, the repeatability of the measurement, any systematic contributions and its uncertainties. (author)

  19. Automatic potentiometric titration study of the iodine content in salt%食盐中碘含量的自动电位滴定法测定研究

    Institute of Scientific and Technical Information of China (English)

    麦浪; 梁雄宇; 黄义活; 梁水基

    2012-01-01

    Objective Establish a fast, easy, accurate iodine in salt content by automatic potentiometric detection method. Methods Determination of iodine content in salt use the Metrohm809 Titrando automatic potentiometric titrator. Results The recovery rate in the different samples was 97,4% -99.0%, relative standard deviation was 0.81% - 1.37%( n =6). It was shown that there was no significant difference between automatic potentiometric titration and direct titration by applying 10 samples( P > 0. 05). Conclusion Automatic potentiometric titration method was simple, rapid and high degree of automation, the determination of iodine content in salt, high accuracy, good reproducibility, conventionally analytical methods for the determination of salt iodine.%目的 建立快速、简便、准确的食盐中碘含量的自动电位滴定检测方法.方法 用瑞士万通Metrohm809 Titrando自动电位滴定仪测定食盐中的碘含量.结果 不同样品中的加标回收率为97.4% ~ 99.0%,相对标准偏差为0.81%~1.37%(n=6),对10份样品分别用自动电位滴定法和直接滴定法测定,两种方法所得结果无显著性差异(P>0.05).结论 自动电位滴定法操作简单、快速,自动化程度高,测定食盐中碘含量时准确度高,重现性好,适合作为盐碘测定的常规分析方法.

  20. Potentiometric titration of uranium reduced by chromic salts in chloridic solutions

    International Nuclear Information System (INIS)

    The utilization of chromic salts for reducing the uranium (VI) from chloridic solutions, for potentiometric dosage is described. This method is used in the range of 0,002 to 1,0 M of uranium. (C.G.C.)

  1. Programa de ajuste multiparamétrico de curvas de titulação potenciométricas de ácidos húmicos Multiparametric adjustment program of potentiometric titration curves of humic acids

    Directory of Open Access Journals (Sweden)

    Clausius Duque Gonçalves Reis

    2010-04-01

    Full Text Available Tendo em vista a dificuldade de determinação dos pontos de inflexão na curva de titulação potenciométrica de ácidos húmicos, por metodologias tradicionais, foi desenvolvido foi desenvolvido um programa na linguagem Delphi para ajuste multiparamétrico de dados de titulação potenciométrica. Para isso um processo iterativo para estimar as raízes de um polinômio, com base no método de Newton-Raphson, foi utilizado. Os dados das titulações potenciométricas de ácidos húmicos usados nas regressões foram obtidos em um sistema automatizado de titulação potenciométrica. O programa desenvolvido na linguagem Delphi permite maior versatilidade e facilidade de operação, com uma interação mais amigável com o usuário. As curvas de titulação potenciométricas ajustadas sobrepuseram-se quase que totalmente às curvas experimentais. Os valores de pKa e as percentagens de grupos tituláveis dos ácidos húmicos, parâmetros ajustáveis na regressão multiparamétrica, apresentaram valores comparáveis com dados da literatura.Regarding the difficulty of determining the inflection points in the potentiometric titration curve of humic acids by means of traditional methodologies, a Delphi program a Delphi program was developed for the multiparametric data adjustment in potentiometric titration. For this purpose, an iterative process was used, based on the Newton-Raphson method to estimate the roots of a polynomial. The humic acid potentiometric titration data, used in regressions, were obtained in an automated system of potentiometric titration. The program developed in Delphi language features greater versatility, ease of operation and better interaction with the user. The adjusted potentiometric titration curves overlap the experimental curves almost entirely. The pKa values and percentages of titrable groups of humic acids extracted from soil, adjustable parameters in the multiparametric regression, were comparable with those reported

  2. Characterization of acid functional groups of carbon dots by nonlinear regression data fitting of potentiometric titration curves

    Science.gov (United States)

    Alves, Larissa A.; de Castro, Arthur H.; de Mendonça, Fernanda G.; de Mesquita, João P.

    2016-05-01

    The oxygenated functional groups present on the surface of carbon dots with an average size of 2.7 ± 0.5 nm were characterized by a variety of techniques. In particular, we discussed the fit data of potentiometric titration curves using a nonlinear regression method based on the Levenberg-Marquardt algorithm. The results obtained by statistical treatment of the titration curve data showed that the best fit was obtained considering the presence of five Brønsted-Lowry acids on the surface of the carbon dots with constant ionization characteristics of carboxylic acids, cyclic ester, phenolic and pyrone-like groups. The total number of oxygenated acid groups obtained was 5 mmol g-1, with approximately 65% (∼2.9 mmol g-1) originating from groups with pKa groups was independent of small variations in experimental conditions, i.e. the mass of carbon dots titrated and initial concentration of HCl solution. Finally, we believe that the methodology used here, together with other characterization techniques, is a simple, fast and powerful tool to characterize the complex acid-base properties of these so interesting and intriguing nanoparticles.

  3. Determination of soil organic matter by automatically potentiometric titration method%自动电位滴定法测定土壤有机质含量

    Institute of Scientific and Technical Information of China (English)

    郝会军; 杨俐苹; 金继运

    2011-01-01

    采用丘林滴定法与自动电位滴定法测定土壤中有机质含量,并对自动电位滴定法做了精密度和加标回收率试验.同时进行了用自动电位滴定法与手工滴定法标定硫酸亚铁标准溶液试验.结果表明,两种方法标定硫酸亚铁标准溶液结果一致,并无显著差别;丘林滴定法和自动电位滴定法均能满足土壤中有机质含量的分析要求,测定结果无显著性差异.自动电位滴定法显示了很好的准确度和重现性,加标回收率在98.43%~101.8%之间,相对标准偏差(RSD)为0.693%~0.936%,可见自动电位滴定法是一种测定土壤有机质含量的好方法.%Soil organic matter (SOM) was determined by Tyurin method with manual titration and automatically potentiometric titration. The precision and recovery rate of automatically potentiometric titration was studied. The concentration of FeSO4 standard solution of was calibrated by both automatically potentiometric titration and manual titration method. The results indicated that there was identical and no remarkable difference for calibration of FeSO4 standard solution by two methods. There was no significance difference for determining SOM by Tyurin method with manual titration and automatically potentiometric titration method which showed two methods could meet analysis requirement. Automatically potentiometric titration method revealed a good accuracy and reproducibility with recovery rate of 98. 43% ~ 101.8% and RSD of 0. 693% ~ 0. 936%. It was obvious automatically potentiometric titration method could be recommended as a good method to determine SOM.

  4. Determination of the biodiesel acidity index by potentiometric titration by using different methods; Determinacao do indice de acidez de biodiesel por titulacao potenciometrica utilizando-se diferentes metodos

    Energy Technology Data Exchange (ETDEWEB)

    Goncalves, Mary Ane; Sobral, Sidney Pereira; Borges, Paulo Paschoal [Instituto Nacional de Metrologia, Normalizacao e Qualidade Industrial (DIMCI/INMETRO), Duque de Caxias, RJ (Brazil). Diretoria de Metrologia Cientifica e Industrial], E-mail: magoncalves@inmetro.gov.br

    2009-07-01

    This work determined the index of the soybean/fat bio diesel through the potentiometric titration. Four different methods were used with variation of solvent and electrodes. The results were compared by F and t (Student) and it was verified that they were agreed in a 95% confidence interval.

  5. Number of independent parameters in the potentiometric titration of humic substances.

    Science.gov (United States)

    Lenoir, Thomas; Manceau, Alain

    2010-03-16

    With the advent of high-precision automatic titrators operating in pH stat mode, measuring the mass balance of protons in solid-solution mixtures against the pH of natural and synthetic polyelectrolytes is now routine. However, titration curves of complex molecules typically lack obvious inflection points, which complicates their analysis despite the high-precision measurements. The calculation of site densities and median proton affinity constants (pK) from such data can lead to considerable covariance between fit parameters. Knowing the number of independent parameters that can be freely varied during the least-squares minimization of a model fit to titration data is necessary to improve the model's applicability. This number was calculated for natural organic matter by applying principal component analysis (PCA) to a reference data set of 47 independent titration curves from fulvic and humic acids measured at I = 0.1 M. The complete data set was reconstructed statistically from pH 3.5 to 9.8 with only six parameters, compared to seven or eight generally adjusted with common semi-empirical speciation models for organic matter, and explains correlations that occur with the higher number of parameters. Existing proton-binding models are not necessarily overparametrized, but instead titration data lack the sensitivity needed to quantify the full set of binding properties of humic materials. Model-independent conditional pK values can be obtained directly from the derivative of titration data, and this approach is the most conservative. The apparent proton-binding constants of the 23 fulvic acids (FA) and 24 humic acids (HA) derived from a high-quality polynomial parametrization of the data set are pK(H,COOH)(FA) = 4.18 +/- 0.21, pK(H,Ph-OH)(FA) = 9.29 +/- 0.33, pK(H,COOH)(HA) = 4.49 +/- 0.18, and pK(H,Ph-OH)(HA) = 9.29 +/- 0.38. Their values at other ionic strengths are more reliably calculated with the empirical Davies equation than any existing model fit. PMID

  6. Synergy Interval Partial Least Square (siPLS) with Potentiometric Titration Multivariate Calibration for the Simultaneous Determination of Amino Acids in Mixtures

    OpenAIRE

    Xiaobo Zuo; Sheng Fang; Xianli Liang

    2014-01-01

    The simultaneous determination of amino acids in solution is important for food and nutrient industries. This study investigated the feasibility of potentiometric titration with synergy interval Partial Least Square (siPLS) for the simultaneous determination of glycine, glutamic acid and phenylalanine in aqueous solution. The methods used were compared with the traditional Partial Least Square (PLS) that based on full pH range. The performance was evaluated by the Root Mean Square Error of Cr...

  7. 自动电位滴定法测定硫磺总酸度%Automatic Potentiometric Titration Determination of Total Acidity in Sulfur

    Institute of Scientific and Technical Information of China (English)

    潘存艳; 齐云鹏; 宁海龙; 张金龙

    2014-01-01

    Basing on samples of imported industrial sulfur in Alashankou port, the automatic potentiometric titration determination of total acidity was established. The titration mode, main titration parameters and the dissolving time of the samples were studied. Each sample tested 10 times, the relative standard deviation was 1. 6560% ~1. 7857%, and in the recovery experiment, the recovery rate was 98. 56% ~101. 02%, which proved that automatic potentiometric titration method possessed high precision and accuracy.%以阿拉山口口岸进口的工业硫磺为样品,建立了测定硫磺总酸度的自动电位滴定法。对滴定模式、主要滴定参数和样品溶解时间进行了探究。每个样品平行测定10次,计算的相对标准偏差为1.6560%~1.7857%;加标回收实验中,得到回收率为95.39%~107.29%,说明了自动电位滴定法精密度很高,同时具有很高的准确度。

  8. Determination of hydroxide in the presence of aluminate using a modified potentiometric titration

    International Nuclear Information System (INIS)

    A procedure for the determination of hydroxide concentration in the presence of aluminate and other interfering ions was developed using the method of standard additions (or more specifically in this case, standard subtractions). The procedure called for titration with a strong acid which was added in equal increments at regular time intervals. The potential was recorded after each addition of acid. The data was plotted on Gran's Plot Paper, which is based on work done originally by Gran, or it was entered into a computer to determine the equivalence volume of the titrant. When used on many different samples in different matrices, the method gave results that were approximately 100 +- 1 percent of the calculated value. This was shown to be true even in systems containing aluminate [Al(OH)4-], phosphate (PO43-), sulfate (SO42-), nitrate (NO3-), nitrite (NO2-), carbonate (CO32-), and other ions. The effect of these ions was shown to be negligible if the initial OH- concentration was at least 10-3 M and barium chloride (BaCl2) was added to complex the PO43- and CO32- ions. These ions were checked at levels of up to 3 M for Al(OH)4- and NO3-, 2 M for NO2-, and 1 M for SO42-, PO43-, and CO32-. The method is applicable to radioactive as well as nonradioactive samples and any heat involved with a radioactive sample is insufficient to cause an error in the determination. On the basis of the work performed it was shown that the method was general enough to be run on a routine basis

  9. Determination of Acidity of Triacetin with Automatic Potentiometric Titration%自动电位滴定法测定三乙酸甘油酯的酸度

    Institute of Scientific and Technical Information of China (English)

    周培琛; 刘泽春; 黄华发; 张峰; 张鼎方; 刘江生; 赖伟玲

    2011-01-01

    为了克服常规酸碱滴定法测定三乙酸甘油酯酸度存在的诸如终点不易观察,相对标准偏差( RSD)较大等缺点,考察了自动电位滴定法.结果表明,自动电位滴定法的RSD为0.774%,定量限0.00175%,回收率99.5%~103.3%.该方法可以快速准确地测定三乙酸甘油酯的酸度.%In order to get rid of the disadvantages of conventional acid-base titration in determining the acidity of triacetin, such as inconvenience in endpoint differentiation and high relative standard deviation, automatic potentiometric titration was investigated. The results showed that the recoveries of the method ranged from 99.5% to 103.3% with the relative standard deviation of 0.774% and the limit of quantitation of 0.00175%. It proved that the acidity of triacetin could be rapidly and accurately determined with automatic potentiometric titration.

  10. 自动电位滴定法测定油脂皂化值%Determination of saponification value of oils and fats by automatic potentiometric titration

    Institute of Scientific and Technical Information of China (English)

    曾正策; 苏军; 吴昊

    2011-01-01

    An automatic potentiometric titration method was established for determining saponification value of oils and fats. Automatic potentiometric titration and the method of GB/T 5534-2008 were separately used to determine the three rapeseed oil samples for 6 times. The relative standard deviations of automatic potentiometric titration and GB/T 5534-2008 were 0. 16% -0. 22% and 0. 36% -0. 81% respectively, so the former was superior to the method of GB/T 5534-2008.%采用电位滴定仪测定了油脂的皂化值,利用电位滴定仪能够识别多个滴定终点的特点,采用分步滴定法用盐酸分别滴定皂化液中过量的氢氧化钾和生成的钾皂,根据滴定钾皂消耗的盐酸的量可计算出样品的皂化值.分别采用全自动电位滴定法和国标GB/T 5534-2008规定的方法对3个不同菜籽油样品各平行测定6次,前者测定结果的相对标准偏差为0.16%~0.22%,优于国标方法测定结果的相对标准偏差0.36%~0.81%.

  11. Determination of sulfides in FCC gasoline by using the potentiometric titration of lead tetraacetate%FCC汽油中硫醚硫的测定--四乙酸铅电位滴定法

    Institute of Scientific and Technical Information of China (English)

    罗立文; 夏道宏

    2004-01-01

    Compared with conventional method of violet spectrum,determination of the content of sulfides in fluid catalytic cracking(FCC)gasoline by using the potentiometric titration of lead tetraacetate has some advantages such as clear potentiometric abrupt change at the stoichiometric point,stable potentiometric value,exact and credible results,and simple operation.The content of sulfides in FCC gasoline of Shenghua refinery is 0.136% by this method.The standard deviation about this method is less than 0.01% and the relative standard deviation is less than 2.42%.

  12. Virtual Instrument for an Automated Potentiometric e-Tongue Employing the SIA Technique

    Directory of Open Access Journals (Sweden)

    Manuel del Valle

    2005-12-01

    Full Text Available In this work we report the design, construction, and applications of an electronictongue (abbreviated e-tongue based on an array of potentiometric sensors employing theSequential Injection Analysis technique (SIA operated as a Virtual Instrument implementedin LabVIEW6.1TM. The system can use transient and stationary responses as the measuredinput information for e-tongues. The new concepts applied, lead to different advantages tobe obtained, such as complete automation, easy handling, saving time, reliability andmodularity.

  13. Kinetics of bacterial potentiometric titrations : the effect of equilibration time on buffering capacity of Pantoea agglomerans suspensions

    OpenAIRE

    Kapetas, Leon; Ngwenya, Bryne T; MacDonald, Alan M.; Elphick, Stephen C.

    2011-01-01

    Several recent studies have made use of continuous acid–base titration data to describe the surface chemistry of bacterial cells as a basis for accurately modelling metal adsorption to bacteria and other biomaterials of potential industrial importance. These studies do not share a common protocol; rather they titrate in different pH ranges and they use different stability criteria to define equilibration time during titration. In the present study we investigate the kinetics of bacterial titr...

  14. Effect of fluoride, chloride, bromide, and thiocynate on potentiometric titrations of iron(II)-tin(II) mixtures with cerium(IV)

    International Nuclear Information System (INIS)

    A two-step curve is expected in the potentiometric titration of Fe(II)-Sn(II) mixtures with Ce(IV) in H2SO4. Each end point should indicate the respective oxidation of Sn(II) and Fe(II). However, experimentally only one end point was found; it corresponded to the total oxidation of Sn(II) and Fe(II). When this oxidation-reduction reaction was carried out in the presence of Cl-, the theoretical behavior was observed. The present study was done to ascertain if monovalent anions other than Cl- have a similar effect on this oxidation-reduction system. The monovalent species F-, Br-, and SCN- were selected for this study, and the results indicate that each affects the rate of reaction relative to the ease of oxidation of the individual ions

  15. Microcalorimetric and potentiometric titration studies on the adsorption of copper by P. putida and B. thuringiensis and their composites with minerals

    International Nuclear Information System (INIS)

    In order to have a better understanding of the interactions of heavy metals with bacteria and minerals in soil and associated environments, isothermal titration calorimetry (ITC), potentiometric titration and equilibrium sorption experiments were conducted to investigate the adsorption behavior of Cu(II) by Bacillus thuringiensis, Pseudomonas putida and their composites with minerals. The interaction of montmorillonite with bacteria increased the reactive sites and resulted in greater adsorption for Cu(II) on their composites, while decreased adsorption sites and capacities for Cu(II) were observed on goethite-bacteria composites. A gram-positive bacterium B. thuringiensis played a more important role than a gram-negative bacterium P. putida in determining the properties of the bacteria-minerals interfaces. The enthalpy changes (ΔHads) from endothermic (6.14 kJ mol-1) to slightly exothermic (-0.78 kJ mol-1) suggested that Cu(II) is complexed with the anionic oxygen ligands on the surface of bacteria-mineral composites. Large entropies (32.96-58.89 J mol-1 K-1) of Cu(II) adsorption onto bacteria-mineral composites demonstrated the formation of inner-sphere complexes in the presence of bacteria. The thermodynamic data implied that Cu(II) mainly bound to the carboxyl and phosphoryl groups as inner-sphere complexes on bacteria and mineral-bacteria composites.

  16. Automatic Potentiometric Titrator Determinated Chloride Ions in Water%自动电位滴定仪测定水中氯离子的探讨

    Institute of Scientific and Technical Information of China (English)

    李芳; 李文胜

    2014-01-01

    Using automatic potentiometric titrator, standard solution of silver nitrate was calibrated and chloride ions in industrial circulating wate was determined. The matters need attention of the electrode maintenance and the end point of titration to set were summarized. The result showed that the determination of chloride ions in water by using the instrument, its accuracy and precision can be obtained satisfactory results.%通过使用自动电位滴定仪标定硝酸银标准溶液和测定工业循环水中氯离子的实验研究,总结了在使用中应注意的电极的维护保养和滴定终点设定方面的一些规律,结果表明用该仪器测定水中氯离子,其准确性和精密度均可获得满意的结果。

  17. Synergy Interval Partial Least Square (siPLS with Potentiometric Titration Multivariate Calibration for the Simultaneous Determination of Amino Acids in Mixtures

    Directory of Open Access Journals (Sweden)

    Xiaobo Zuo

    2014-11-01

    Full Text Available The simultaneous determination of amino acids in solution is important for food and nutrient industries. This study investigated the feasibility of potentiometric titration with synergy interval Partial Least Square (siPLS for the simultaneous determination of glycine, glutamic acid and phenylalanine in aqueous solution. The methods used were compared with the traditional Partial Least Square (PLS that based on full pH range. The performance was evaluated by the Root Mean Square Error of Cross-Validation (RMSECV, the Root Mean Square Error of Prediction (RMSEP and the correlation coefficient (R. By optimizing the pH region with siPLS, a good linear model was produced for the calibration set with correlation coefficient R of 0.9947, 0.9956 and 0.9913 for glycine, glutamic acid and phenylalanine, respectively. A single set of synergy mixtures was tested independently and good results were obtained. The results show that the siPLS method can locate the informative region by using a graphically-oriented interface which is more easily to use and interpret. The study proves the feasibility of potential titration with chemometrics in the simultaneous determination of amino acid mixtures without preliminary separation.

  18. Microcalorimetric and potentiometric titration studies on the adsorption of copper by P. putida and B. thuringiensis and their composites with minerals

    Energy Technology Data Exchange (ETDEWEB)

    Fang Linchuan [State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070 (China); Key Laboratory of Subtropical Agriculture and Environment, Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070 (China); Cai Peng; Li Pengxiang; Wu Huayong; Liang Wei; Rong Xingmin [Key Laboratory of Subtropical Agriculture and Environment, Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070 (China); Chen Wenli [State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070 (China); Huang Qiaoyun, E-mail: qyhuang@mail.hzau.edu.cn [State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070 (China); Key Laboratory of Subtropical Agriculture and Environment, Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070 (China)

    2010-09-15

    In order to have a better understanding of the interactions of heavy metals with bacteria and minerals in soil and associated environments, isothermal titration calorimetry (ITC), potentiometric titration and equilibrium sorption experiments were conducted to investigate the adsorption behavior of Cu(II) by Bacillus thuringiensis, Pseudomonas putida and their composites with minerals. The interaction of montmorillonite with bacteria increased the reactive sites and resulted in greater adsorption for Cu(II) on their composites, while decreased adsorption sites and capacities for Cu(II) were observed on goethite-bacteria composites. A gram-positive bacterium B. thuringiensis played a more important role than a gram-negative bacterium P. putida in determining the properties of the bacteria-minerals interfaces. The enthalpy changes ({Delta}H{sub ads}) from endothermic (6.14 kJ mol{sup -1}) to slightly exothermic (-0.78 kJ mol{sup -1}) suggested that Cu(II) is complexed with the anionic oxygen ligands on the surface of bacteria-mineral composites. Large entropies (32.96-58.89 J mol{sup -1} K{sup -1}) of Cu(II) adsorption onto bacteria-mineral composites demonstrated the formation of inner-sphere complexes in the presence of bacteria. The thermodynamic data implied that Cu(II) mainly bound to the carboxyl and phosphoryl groups as inner-sphere complexes on bacteria and mineral-bacteria composites.

  19. 等电位间隔电位滴定法测定葡萄酒中游离二氧化硫%Determination of free sulfur dioxide in wine by the equal potential interval potentiometric titration

    Institute of Scientific and Technical Information of China (English)

    冯俊贤; 李家栋; 孙晓丽; 苏洪茹; 刘元昀

    2013-01-01

    目的:建立等电位间隔电位滴定法测定葡萄酒中游离SO2的方法.方法:采用间接碘量滴定,以等电位间隔法识别滴定终点.结果:方法RSD≤0.5%,游离二氧化硫回收率在94.50% ~ 103.7%,与自动电位滴定法比较,相对误差小于1.0%.结论:间接碘量法无需碘标准溶液,等电位间隔电位滴定法识别滴定终点准确可靠,重现性好,适合葡萄酒中游离二氧化硫含量的测定.%Objective:To establish a method for determination of free sulfur dioxide in wine by the equal potential interval potentiometric titration. Methods: According to indirect iodimetry, the end - point of titration could be judged with the equal potential interval potentiometric titration. Results: The RSD was 0.3% ~0.5% , the recovery rate for free sulfur dioxide was 94. 50% ~ 103. 7%. Compared with automatic potentiometric titration, the relative deviation for free sulfur dioxide was less than 1.0%. Conclusion: The indirect iodimetry is simple, accurate without iodine standard solution. The equal potential interval potentiometric titration is accurate, reliable with good repeatability. It is suitable for determination of free sulfur dioxid in wine.

  20. Development of a Novel Solid-State Sensor Electrode Based on Titanium Thin Film as an Indicator Electrode in Potentiometric and Conductometric Acid-Base Titration in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Nasser Abu Ghalwa

    2012-01-01

    Full Text Available A modified Ti/(SnO2 + Sb2O3 electrode was prepared by thermal deposition on titanium substrate and its use as indicator electrode to potentiometric and conductometric acid-base titration in aqueous solution at 298 K was developed. The E-pH curve is linear with slope of 0.0512 V/dec at 298 K. The standard potential of this electrode, E0, was determined with respect to the SCE as reference electrode. The recovery percentages for potentiometric and conductometric acid-base titration for acetic acid against NaOH were calculated. The cell constant, specific conductance, and the molar conductance with dilution for some common electrolytes were measured.

  1. 自动电位滴定法测定米糠油酸值的研究%Detection of acid value of rice bran oil by automatic potentiometric titration

    Institute of Scientific and Technical Information of China (English)

    薛斌; 曹文明; 包杰; 陈纯; 金俊

    2014-01-01

    为了克服传统的人工指示剂滴定法在测定米糠油酸值过程中,米糠油本身的颜色和高含量的γ-谷维素对测定结果的严重干扰,采用自动电位滴定法,根据经典的酸碱滴定理论,采用二次作图法,在滴定的同时由联机电脑实时同步绘制酸碱滴定的pH-滴定体积曲线及其相应的一阶微分曲线,以这些曲线上游离脂肪酸发生中和反应引起的“pH突跃”为滴定终点的判定依据,建立米糠油酸值测定的自动电位滴定法。结果发现,自动电位滴定法能够准确区分游离脂肪酸和γ-谷维素各自的滴定终点,从而排除γ-谷维素对米糠油酸值测定的干扰。对比实验发现,除了米糠油外,自动电位滴定法对各类食用植物油酸值的测定结果与传统的人工指示剂滴定法的测定结果十分接近;但对于米糠油,人工指示剂滴定法的酸值(KOH)测定结果一般偏高0.3~1.0 mg/g。表明自动电位滴定法更能准确地测定米糠油的酸值。%In order to overcome the severe interferences of color and high contentγ-oryzanol in the de-tection of acid value of rice bran oil by traditional manual indicator titration method, according to the classical theory of acid base titration, using methods of automatic potentiometric titration and “second graph”, a detection method of the acid value of rice bran oil was established. Using this method, the pH-titration volume curve and corresponding first -order difference curve of acid base titration were drawn by computer real-timely and synchronously, then the “pH jump” in these curves, which was caused by the neutralization of free fatty acids, was taken as the foundation for judgment of titration end point. The results showed that the titration end points of free fatty acids and γ-oryzanol could be distin-guished correctly by automatic potentiometric titration method, therefore the interference of γ-oryzanol in the detection

  2. 全自动电位滴定法测定有色液态食品中的糖含量%Determination of sugar content in colored liquid food by automatic potentiometric titration

    Institute of Scientific and Technical Information of China (English)

    纪丽君; 陈英; 李培; 姚卫蓉

    2013-01-01

    本论文针对国标法测定糖含量所采用的手工滴定法存在不适合深色样品的缺点,研究采用高温氧化还原电极的全自动滴定法进行替代的可能性.首先通过测定3个含酒精饮料,研究样品中的酒精对全自动滴定结果的影响,结果表明有色液态样品中所含酒精对全自动电位滴定法测定结果没有影响;采用全自动电位滴定法测定了9个有色液态食品(包括7个含酒精饮料和2个碳酸饮料)的糖含量,相对标准偏差(RSD)、回收率分别为0.124% ~ 1.637%、96.0% ~104.6%,并将结果与国标方法的结果进行了比对,相关系数r达到0.99997,说明全自动电位滴定法作为糖含量测定的一种新方式,其精密度和准确度均满足要求,可以取代传统手工滴定法.%The traditional manual titration method for determination sugar is not so suitable for the dark samples to overcome this shortcorning.A replace method of automatic potentiometric titrator equipped with high temperature redox electrode was studied,Firstly,the effect of alcohol on the determiantion result was stuidied by detecting 3 kinds of alcoholic beverage, which showed no effect.Then the sugar content of 9 kinds of colored liquid food, including 7 alcoholic beverage and 2 sodas, were measured by automatic potentiometric titration.Their relative standard deviation( RSD) and recoveries were 0.124% ~ 1.637% and 96.0%~104.6% respectively.The correlation between automatic potentiometric titration and manual titration was 0.99997. Our result showed that the automatic potentiometric titration method could meet the demand of detection sugar and could replace of the manual titration method.

  3. Preliminary Discussion on Development of Automatic Potentiometric Titration Technology and Its Application to Routine Detection of Solution%浅谈自动电位滴定技术发展及在常规检测中的应用

    Institute of Scientific and Technical Information of China (English)

    王桂林; 陶淑芸

    2013-01-01

    According to the simple and quick,accurate and efficient advantages,the application of automatic potentiometric titration technology in the detection industry is becoming increasingly popular. This article describes the development of the potentiometer titration method,and analyses the principle,to study the application in routine detection,compared with direct potential. Compared through experiments by automatic potentiometric titrator and the traditional manual titration,the results showed no significant difference.%  自动电位滴定技术因其简便快捷、准确高效的优点在检测行业的应用越来越普及。介绍了电位滴定法的发展,分析其原理,研究其在常规检测中的应用,比较其与直接电位法的区别,并使用自动电位滴定仪与传统人工滴定进行实验对比,得出无显著性差异结果。

  4. Determination of total manganese in manganese ore by automatic potentiometric titrator%自动电位滴定仪测定锰矿石中全锰量

    Institute of Scientific and Technical Information of China (English)

    马德起; 韩娟; 胡德新; 武素茹; 王永芳

    2012-01-01

    样品经盐酸、磷酸、硝酸、高氯酸加热溶解后,以硫酸亚铁铵为标准溶液为滴定液,采用自动电位滴定仪测定全锰量.经过对5个有证标准样品进行测试,全锰量测定的平均值与认定值的误差在0.015%~0.145%之间,标准差为0.074%,t检验值为0.366.选取主要进口国含量不同的样品进行全锰量的测定,并进行方法对比,其允许差符合标准GB/T 1506-2002规定.本法具有较高灵敏度和准确度,可用于大批量锰矿石的日常检测.%The sample was dissolved in hydrochloric acid, phosphoric acid, nitric acid and perchloric acid by heating. The content of total manganese was determined by automatic potentiometric titrator. Five certified reference materials were tested. The errors between average determination value and certified value of total manganese content were in the range of 0. 015 %-0. 145%. The standard deviation was 0. 074% and the t test value was 0. 366. Various samples with difference total manganese contents from main import countries were selected for the determination of total manganese. The method comparison was conducted, and the admissible error complied with rules in GB/T 1506-2002. This method had high sensitivity and accuracy, and it could be used for the routing inspection of large numbers of manganese ores.

  5. Studies of factors affecting uranium determinations by automated coulometric titration (New Brunswick Laboratory/Davies--Gray Method)

    International Nuclear Information System (INIS)

    The method's errors are defined to ascertain its absolute accuracy. An analytical technique was developed to examine vanadyl sulfate diluent for vanadium (V). None could be found in any of the lots tested. Certain lots of reagent-grade phosphoric acid contained an unidentified impurity that caused high generator-electrode potentials and a positive error. The current-potential characteristics of the generator electrode were measured. The data indicated that a significant fraction of uranium (IV) was oxidized directly during the early stages of titration. Using equations theoretically applicable to such a titration, a negligible difference was found between the inflection point of the titration curve and the equivalence point in the titration. However, the actual experimental curves did not agree with the theoretical curves early in the titration. Measurements of the background current indicated a level equivalent to approximately 0.2 mg uranium. The evaluation of the reagent delivery system used in the automated analyzer revealed adequate reproducibility. 8 tables

  6. Instrumentation and Automated Photometric Titration Procedure for Total Acidity Determination in Red Wine Employing a Multicommuted Flow System

    OpenAIRE

    Boaventura F. Reis; Ausberta Jesus Cabezas Garcia

    2006-01-01

    An automated procedure for photometric titration of red wine and associated instrumentation is described. The procedure was based on the flow-batch approach implemented employing multicommutation. The photometric detection was carried out using a homemade LED-based photometer. The mixing device, LED, and photodetector were attached to the titration chamber in order to form a compact and small-sized unit. The flow system comprised an automatic injector and three-way solenoid valves, which were...

  7. Automatic Potentiometric Titration Method to Measure the Different Types of Wine in the Total Acid Ester and Comparison of the Total%自动电位滴定法测不同类酒中的总酸总酯

    Institute of Scientific and Technical Information of China (English)

    杨盛春; 杨明惠; 高云涛

    2013-01-01

    Total acid and total alcohol ester is an important indicator of the two, the quality of the wine production and has a great influence. Conventional methods of determination of total acid titration method directly, pH meter and so on, while the total esters are used saponification were determined by neutralization. As two indicators were measured, and both manual systems and thus easy to operate, big error. In the paper, the analysis by automatic potentiometric titration to determine by potentiometric titration Category 3 of 6 total acid total ester alcohol, obtained satisfactory results.%  总酸与总酯是酒分析中的两个重要指标,对酒的生产及其品质有很大的影响。常规检测总酸的方法有直接滴定法、酸度计法等,而总酯则采用皂化中和法加以测定。由于二项指标分别测定,且均系手工操作,因而操作繁琐,误差较大。文章应用自动电位滴定法进行分析,测定了3类6种酒中总酸与总酯的含量,获得了较为满意的结果。

  8. Method of semi-automatic high precision potentiometric titration for characterization of uranium compounds; Metodo de titulacao potenciometrica de alta precisao semi-automatizado para a caracterizacao de compostos de uranio

    Energy Technology Data Exchange (ETDEWEB)

    Cristiano, Barbara Fernandes G.; Dias, Fabio C.; Barros, Pedro D. de; Araujo, Radier Mario S. de; Delgado, Jose Ubiratan; Silva, Jose Wanderley S. da, E-mail: barbara@ird.gov.b, E-mail: fabio@ird.gov.b, E-mail: pedrodio@ird.gov.b, E-mail: radier@ird.gov.b, E-mail: delgado@ird.gov.b, E-mail: wanderley@ird.gov.b [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Lopes, Ricardo T., E-mail: ricardo@lin.ufrj.b [Universidade Federal do Rio de Janeiro (LIN/COPPE/UFRJ), RJ (Brazil). Coordenacao dos Programas de Pos-Graduacao de Engenharia. Lab. de Instrumentacao Nuclear

    2011-10-26

    The method of high precision potentiometric titration is widely used in the certification and characterization of uranium compounds. In order to reduce the analysis and diminish the influence if the annalist, a semi-automatic version of the method was developed at the safeguards laboratory of the CNEN-RJ, Brazil. The method was applied with traceability guaranteed by use of primary standard of potassium dichromate. The standard uncertainty combined in the determination of concentration of total uranium was of the order of 0.01%, which is better related to traditionally methods used by the nuclear installations which is of the order of 0.1%

  9. The measurement of alkalinity in the Raney nickel catalyst activation by Automatic potentiometric titration%自动电位滴定法测定Raney镍催化剂活化中的碱度

    Institute of Scientific and Technical Information of China (English)

    叶乃义

    2011-01-01

    This research studies the method of potentiometric titration to determinate the concentration of NaOH in the lotion off in the activativity process of Raney nickel catalyst.It can meet the testing demand of Raney nickel catalyst to activation and possesses its application values in the actual work.%本文研究采用电位滴定法测定Raney镍催化剂在活化过程中脱洗液中NaOH含量,能够满足Raney镍催化剂活化时的检测需求,具有实际的工作应用价值。

  10. Automated high-pressure titration system with in situ infrared spectroscopic detection

    Science.gov (United States)

    Thompson, Christopher J.; Martin, Paul F.; Chen, Jeffrey; Benezeth, Pascale; Schaef, Herbert T.; Rosso, Kevin M.; Felmy, Andrew R.; Loring, John S.

    2014-04-01

    A fully automated titration system with infrared detection was developed for investigating interfacial chemistry at high pressures. The apparatus consists of a high-pressure fluid generation and delivery system coupled to a high-pressure cell with infrared optics. A manifold of electronically actuated valves is used to direct pressurized fluids into the cell. Precise reagent additions to the pressurized cell are made with calibrated tubing loops that are filled with reagent and placed in-line with the cell and a syringe pump. The cell's infrared optics facilitate both transmission and attenuated total reflection (ATR) measurements to monitor bulk-fluid composition and solid-surface phenomena such as adsorption, desorption, complexation, dissolution, and precipitation. Switching between the two measurement modes is accomplished with moveable mirrors that direct the light path of a Fourier transform infrared spectrometer into the cell along transmission or ATR light paths. The versatility of the high-pressure IR titration system was demonstrated with three case studies. First, we titrated water into supercritical CO2 (scCO2) to generate an infrared calibration curve and determine the solubility of water in CO2 at 50 °C and 90 bar. Next, we characterized the partitioning of water between a montmorillonite clay and scCO2 at 50 °C and 90 bar. Transmission-mode spectra were used to quantify changes in the clay's sorbed water concentration as a function of scCO2 hydration, and ATR measurements provided insights into competitive residency of water and CO2 on the clay surface and in the interlayer. Finally, we demonstrated how time-dependent studies can be conducted with the system by monitoring the carbonation reaction of forsterite (Mg2SiO4) in water-bearing scCO2 at 50 °C and 90 bar. Immediately after water dissolved in the scCO2, a thin film of adsorbed water formed on the mineral surface, and the film thickness increased with time as the forsterite began to dissolve

  11. 自动电位滴定法快速测定铝箔生产液中的氯离子%Automtic potentiometric titration determinated chloride ions in electrolyte

    Institute of Scientific and Technical Information of China (English)

    林庆宇; 张志; 罗杨合; 练洁婷

    2011-01-01

    利用自动电位滴定仪,在体积分数为80%的丙酮介质中,以Ag电极为指示电极,双盐桥甘汞电极为参比电极,对铝箔生产液中Cl-进行非水滴定,方法的电位突跃明显,电极响应速度较快,SO42-、Cu2+、Fe3+及可能存在其他离子均对测定结果无影响,实现了自动电位滴定法快速测定铝箔生产过程液中Cl-的含量,结果表明本法是一种测定Cl-含量的有效方法.%Using automatic potentiometric titration, chlorine ions in aluminum electrolyte was determined at 80% acetone medium, with the silver electrode as indicator electrode, double salt bridge calomel electrode as reference electrode. The end point jumped of method over 500mV, the electrode responsed faster. Sulfate, copper ions, iron ions and other ions were no effect on the determination. The result showed that content of chloride could be achieved quickly by automatic potentiometric titration. It is an effective way to determine of industry chloride ion.

  12. 自动电位滴定法测定马蹄中的总还原糖%Determination of Reducing Sugar in Eleocharis dulcis by Automatic Potentiometric Titration

    Institute of Scientific and Technical Information of China (English)

    林庆宇; 张志; 魏小平; 严瑶

    2011-01-01

    [Objective] To study the new system for determining the reducing sugar in Eleocharis dukis by automatic potentiometric titration. [ Method] According to the principles of Film's indirect iodometric method,the automatic potentiometric titration was adopted to detect the con tent of reducing sugar,and the optimal conditions of the system were determined. [ Result] The standard deviation detected by the method was 2.47% ,RSD was 1. 30% , the added recovery was 99. 2% - 102. 5% ,and the average recovery was 99. 26%. [ Conclusion] The method was easy,rapid and accurate,which provided effective method for determining the sugar content of fruit products.%[目的]研究自动电位滴定法测定马蹄中总还原糖含量的新体系.[方法]根据菲林氏间接碘量法的原理,应用自动电位滴定法测定,确定了体系的最优条件.[结果]方法测定的标准偏差为2.47%,RSD为1.30%,加标回收率为99.2% ~ 102.5%,平均回收率为99.26%.[结论]该法操作简便快速、结果准确,为果品糖分含量提供有效的测定方法.

  13. Determinação de ácido acéttico em amostra de vinagre adulterada com ácido clorídrico - um experimento integrado de titulação potenciométrica e condutométrica Determination of acetic acid in vinegar adulterated sample with cloridric acid - an experiment integrated of potentiometric and conductometric titrations

    Directory of Open Access Journals (Sweden)

    José Vinicius Martins

    2010-01-01

    Full Text Available The determination of acetic acid in vinegar adulterated sample using simultaneous potentiometric and condutometric titrations was used as an example of integrated experiment in instrumental analysis. An Excel® spreadsheet, which allows the entry of simultaneous data and the construction of the superimposed experimental curves (condutometric, potentiometric, first and second derivative potentiometric curve and, distribution diagrama of the acetic species as function of pH, was used as powerful tool to discuss the fundamental concepts involved in each technique and choose the best of them to quantify, without mutual interference, H3CCOOH and HCl in vinegar adulterated sample.

  14. Determination for acid and peroxide value in nuts by potentiometric titration method%电位滴定法测定坚果食品中的酸价和过氧化值

    Institute of Scientific and Technical Information of China (English)

    王国桢; 苏菊萍; 刘俐君; 李丹; 董琳; 王萍

    2015-01-01

    目的:建立坚果食品中酸价和过氧化值的电位滴定检测方法。方法本试验采用石油醚对坚果食品试样进行浸提,过滤后用旋转蒸发仪对试剂回收利用,并将浸提出的油脂用电位滴定法测定酸价和过氧化值,计算出坚果食品中酸价和过氧化值结果。结果选择瓜子、花生、杏仁、核桃4类坚果,不同实验室重复测定16次,酸价的电位滴定结果:0.29~4.09 mg/g,相对标准偏差:0.64%~3.63%;过氧化值的电位滴定结果:0.011~0.071 g/100 g,相对标准偏差:1.28%~8.77%。电位滴定结果与手动滴定结果相比较,无显著性差异(P>0.05)。结论坚果食品中酸价和过氧化值的电位滴定检测方法操作简单,结果准确度能满足国标要求,且灵敏度高,精密度好。%Objective To establish a testing method for determination of acid and peroxide value in nuts by potentiometric titration. Methods The nuts samples were extracted by the petroleum ether, the reagent after filtration was recycled with the rotary evaporator, the acid and peroxide value of the extraction of oil were tested by potentiometric titration, and then the results of acid and peroxide value in nuts were calculated. Results The melon-seeds, peanuts, almonds and walnuts as samples were used to detect in different labs, the results of acid value were 0.29~4.09 mg/g, the RSD was 0.64~3.63%, the results of peroxide value were 0.011~0.071 g/100 g, and the RSD was 1.28~8.77%. There is no significant difference between potentiometric titration and manual titration (P>0.05). Conclusion The method is simple, accurate, sensitive, and of high precision. It can be used to detect acid and peroxide value in nuts.

  15. Instrumentation and automated photometric titration procedure for total acidity determination in red wine employing a multicommuted flow system.

    Science.gov (United States)

    Garcia, Ausberta Jesus Cabezas; Reis, Boaventura F

    2006-01-01

    An automated procedure for photometric titration of red wine and associated instrumentation is described. The procedure was based on the flow-batch approach implemented employing multicommutation. The photometric detection was carried out using a homemade LED-based photometer. The mixing device, LED, and photodetector were attached to the titration chamber in order to form a compact and small-sized unit. The flow system comprised an automatic injector and three-way solenoid valves, which were controlled by a microcomputer through an electronic interface card. The software, written in Quick BASIC 4.5, was designed with abilities to accomplish all steps of the titration procedure including data acquisition and real-time processing to decide about the course of titration in the following step and so forth, until the titration endpoint was reached. The usefulness of the proposed titration system was demonstrated by analyzing red wine samples. When results were compared with those obtained using the AOAC reference method, no significant difference was observed at the 95% confidence level. A relative standard deviation of ca 2% (n=9) was obtained when processing a typical red wine sample containing 7.3 gl-1 total acidity expressed as tartaric acid. PMID:17671625

  16. Instrumentation and Automated Photometric Titration Procedure for Total Acidity Determination in Red Wine Employing a Multicommuted Flow System

    Directory of Open Access Journals (Sweden)

    Boaventura F. Reis

    2006-09-01

    Full Text Available An automated procedure for photometric titration of red wine and associated instrumentation is described. The procedure was based on the flow-batch approach implemented employing multicommutation. The photometric detection was carried out using a homemade LED-based photometer. The mixing device, LED, and photodetector were attached to the titration chamber in order to form a compact and small-sized unit. The flow system comprised an automatic injector and three-way solenoid valves, which were controlled by a microcomputer through an electronic interface card. The software, written in Quick BASIC 4.5, was designed with abilities to accomplish all steps of the titration procedure including data acquisition and real-time processing to decide about the course of titration in the following step and so forth, until the titration endpoint was reached. The usefulness of the proposed titration system was demonstrated by analyzing red wine samples. When results were compared with those obtained using the AOAC reference method, no significant difference was observed at the 95% confidence level. A relative standard deviation of ca 2% (n=9 was obtained when processing a typical red wine sample containing 7.3 gl-1 total acidity expressed as tartaric acid.

  17. Separate Determination of Borohydride, Borate, Hydroxide, and Carbonate in the Borohydride Fuel Cell by Acid-Base and Iodometric Potentiometric Titration

    OpenAIRE

    Churikov, A. V.; S. L. Shmakov; Romanova, V. O.; Zapsis, K. V.; Ushakov, A. V.; Ivanishchev, A. V.; Churikov, M. A.

    2014-01-01

    A methodology for quantitative chemical analysis of the complex “borohydride-borate-hydroxide-carbonate-water” mixtures used as fuel in the borohydride fuel cell was developed and optimized. The methodology includes the combined usage of the acid-base and iodometric titration methods. The acid-base titration method, which simultaneously uses the technique of differentiation and computer simulation of titration curves, allows one to determine the contents of hydroxide (alkali), carbonate, and ...

  18. 自动电位滴定仪测定铁矿石中全铁量的自动化程序设计%Program designing for determination of total iron content in iron ore by automatic potentiometric titrator

    Institute of Scientific and Technical Information of China (English)

    马德起; 武素茹; 臧世阳

    2012-01-01

    本文采用微波消解—自动电位滴定法测定铁矿石全铁量.重点研究自动电位滴定仪编写空白的滴定程序编写的方式对结果的影响、设计滴定程序,以经典的手工滴定法作对比,结果相似,达到滴定过程的自动化.结果表明:本法适用于铁矿石中全铁量的检测,测定范围为40%~70%,相对标准偏差小于2%.%A method based on Time Slice Model (TSM) is proposed for batch processes heat exchanger network synthesis by taking place. Total iron content in iron ore was determined by automatic potentiometric titrator and the sample was digested by microwave. The program designing for blank was discussed which effect on the results, and also the program designing for total titration, and then the results conformed to the manual titration method. The method applies to determination of total iron content in iron ore, the inspection range was 40%~70%, RSD

  19. Determination of the content of sodium acetate anhydrous by aqueous potentiometric titration method%水相电位滴定法测定无水乙酸钠含量

    Institute of Scientific and Technical Information of China (English)

    杨晓丽

    2011-01-01

    将无水NaAc配成水溶液,用自动电位滴定仪,以DETU滴定模式水相滴定法快速准确分析无水NaAc主体含量.结果表明,无水NaAc溶液浓度为0.1000mol· L-1时,滴定结果与国家标准方法分析结果基本一致,允许误差小于0.2%;标准偏差为0.030~0.057,相对标准偏差为0.030%~0.057%.%The anhydrous sodium acetate is prepared into water solution, The main content of anhydrous sodium acetate was determined by DETU aqueous titration method with automatic potentiometric titration.The results show that, anhydrous sodium acetate solution concentration was 0.1000 mol'L-1, GB/T titration and 694-1995 analysis results are basically consistent, allowable error is less than 0.2%; the standard deviation was 0.030-0.057, the relative standard deviation is 0.030%~0.057%.

  20. 自动电位滴定仪在铜元素分析中的应用研究%Analysis of Copper Element Using Automatic Potentiometric Titration Method

    Institute of Scientific and Technical Information of China (English)

    黄乐斯; 徐美娇; 彭娜; 彭锦锋; 吴文进; 范远红

    2011-01-01

    利用自动电位滴定仪,建立了铜合金和铜矿石中铜含量检测的一种新方法。结果表明:用二阶微商法确定滴定终点为245 mV,在预控点设置为310 mV,滴定剂硫代硫酸钠标准溶液浓度为0.01 mol/L滴定,pH在3~4之间时,加入2 mL氟化氢铵,取10 mL消解液的滴定结果较接近,且标准偏差较小,精密度高,测定结果准确。%Using automatic potentiometric titration instrument,a new method to examine the copper alloy and copper copper content palygorskite was established.5 kinds of titration parameters,like precontrol point setting,concentration of titrant,solution of to be tested acidity,addition amount of ammonium bifluoride and amount of testing solution were researched.Using second-order micro business method to judge titration end volume and abrupt jump potential points.At the best possible conditions,the copper alloy and copper ore content was determined by nitric acid digestion method.And make a comprehensive analysis on its precision and recovery percent.The results showed that the two order derivative method to determine the end point of titration for the 245 mV,in control point was set to 310 mV,the titration of sodium thiosulfate standard solution concentration was 0.01 mol/L titration,pH in 3~4,2 mL ammonium hydrogen fluoride,and 10 mL digestion liquid titration results were very close.The measuring result was accurate,with high precision and litter deviation.

  1. 多项目电位滴定系统在工业锅炉水质检测中的应用%The Usage of Automatic Potentiometric Titration in Industrial Boiler Water-treatment

    Institute of Scientific and Technical Information of China (English)

    黄容; 张居光; 邱康勇

    2012-01-01

    在工业锅炉水质检测中采用多项目电位滴定系统实现锅炉水中的pH、碱度、氯离子等多项目的同步检测,检测过程可溯源,检测效率高。该检测方法重复性符合相关标准,与手动测定结果的比对试验的相对平均偏差低于2%,回收率97%~105%。%By means of automatic potentiometric titration,multi-items of industrial boiler water-treatment such as pH,alkalinity,chlorinity can be synchronous detected.This detection method is traceable and efficient.The relative average deviation of comparative test is less than 2 %.The result of recovery test was 97 %~105 %.

  2. 自动电位滴定仪测定海洋沉积物中碳酸盐百分含量%THE DETERMINATION OF CARBONATE CONTENT IN MARINE SEDIMENTS BY AUTOMATIC POTENTIOMETRIC TITRATOR

    Institute of Scientific and Technical Information of China (English)

    孙晗杰; 李铁刚; 于心科

    2012-01-01

    Based on the volumetric method, the determination of carbonate content in marine sediment was carried out by automatic potentiometric titrator with related software-tiamo, which can export the results automatically. This method is simple and rapid for batch measurement. The results were consistent with standards defined by the National Standard Reference of Deep-Sea Sediment. Seven independent determinations were measured for the same sample, and the standard deviation of the results was less than 0. 9 %. Several samples of sediment core MD06-3050 were used to measure carbonate content by automatic potentiometric titrator and ICP-OES. The results of two methods were consistent.%基于容量法原理,探讨了海底沉积物中碳酸盐的自动电位滴定法,配合tiamo软件,自动计算并输出测定结果.该法简单快速,且可以批量测试,经深海沉积物等国家标准物质验证,结果与标准值相符.对同一样品进行7次测定,其结果的相对标准偏差小于0.9%.该方法应用于西菲律宾海岩心MD06-3050的部分样品,测试结果与ICP-OES方法得到的结果具有一致性,该方法再现性良好,准确可信.

  3. Uncertainty Evaluation for the Determination of Chromium in Ferrochromium by Automatic Potentiometric Titration%自动电位滴定法测定铬铁中铬含量的不确定度评定

    Institute of Scientific and Technical Information of China (English)

    赵晶晶

    2013-01-01

    建立了自动电位滴定法测定铬铁中铬含量的数学模型,对数学模型中各个参数进行不确定度来源分析,分别对A类不确定度及B类不确定度进行评定,对各不确定度分量进行合成,得到铬质量分数的不确定度。当铬铁中铬含量为68.31%时,扩展不确定度为0.52%(k=2)。结果表明玻璃器具的精度、自动电位滴定仪自带体积管的误差、自动电位滴定仪终点识别的误差是测量不确定度的主要来源。%A mathematics model for evaluating the uncertainty for the determination of chromium in ferrochromium by automatic potentiometric titration was established. The uncertainty sources for each of the parameters in the model were analyzed. The uncertainties of type A or type B were evaluted. According to the method,the component uncertainties were synthesized, which were used to obtain the uncertainty evalution. The expanded uncertainty was 0.52%(k=2) as chromium content in errochromium was 0.52%.The results showed that the accuracy of glassware, inaccuracy from prover of automatic potentiometric titration and error from end identification were the main sources for uncertainties.

  4. 自动电位滴定仪测定水中氯化物的应用研究%Application Research on the Determination of Chloride in Water by Automatic Potentiometric Ti-tration Instrument

    Institute of Scientific and Technical Information of China (English)

    窦蓓蕾; 杏艳; 王舒婷; 郭晋君; 田渭花

    2014-01-01

    Determination of water by automatic potentiometric titration of chloride,can get high precision and accuracy,the quality control result in confidence.Compared with the traditional manual titration method, with a lower detection limit,is not affected by the turbidity and chroma of the determination of water,more suitable for low concentration of water samples and special water sample,worthy of promotion in environ-mental monitoring system.%采用自动电位滴定仪测定水中的氯化物,可得到较好的精密度及准确度,经质控样测定结果可信。与传统手工滴定法相比较,该方法具有更低的检出限,且不受水体浊度及色度的影响,更适用于低浓度水样和特殊水样的测定,值得在环境监测系统中推广应用。

  5. Determination of Chloride with Automatic Potentiometric Titration%自动电位滴定仪测定氯化物的探讨

    Institute of Scientific and Technical Information of China (English)

    李莉; 郑璇; 赵彬; 肖溶

    2012-01-01

    该实验就自动电位滴定仪测定氯化物的检出限、适用的水样pH范围及对其干扰物质的最大容忍浓度作了实验研究,对分析实际水样有一定的参考作用.%The detection limit, applicable pH and interference tolerance to chloride in the automatic potentiometric titrationwere discussed, which would be beneficial to the analysis of chloride.

  6. Quantitative determination of alkylcarboxylbetaine surfactants by automatic potentiometric titration%自动电位滴定法定量测定烷基羧基甜菜碱类表面活性剂含量

    Institute of Scientific and Technical Information of China (English)

    王海江; 戚晶晶; 许宗会; 郑昌戈; 崔正刚

    2012-01-01

    Quantitative determination of a series of alkylcarboxylbetaines by automatic potentiometric titration was studied with emphases as effect of selection of acidification agents, acidification temperature and time on the titralion result with respect to the content of alkylcarboxylbetaines. The results showed that the determination accuracy is significantly affected by the pH of the acidification system as well as the acidification temperature and time. Key issue is to assure the complete acidification of the alkylcarboxylbetaine molecules. By using acetic acid - sodium acetate buffer solution of pH = 3 as acidification system at 70 ~ 80 ℃ for 2 -3 h,the content of C12 - C18 alkyldimethylcarboxylbetaines and bis - dodecylmethylcarboxylbetaine can be potentiometric titrated by sodium dodecyl sulfate (SDS) with satisfactory result and the recovery achieves 97% - 102%. Good results have also be obtained by acidification in sulfuric acid solution of pH = 2 for 1 h at room temperature. For samples of technical grade betaine product, under the titration conditions, content of tertiary amine in the product will participate the titration reaction,so that the titration result is actually the sum of content of alkylbetaine and corresponding tertiary amine. Since the tertiary amine content can be independently measured using suitable method,the content of alkylbetaine can thus be quantitatively identified.%研究了酸化剂种类、酸化温度及时间等对电位滴定法测定烷基摹羧基甜菜碱含量的影响.结果表明,酸化剂的pH,酸化温度和时间等对测定结果有显著影响,关键是保证甜菜碱分子的完全酸化.以pH =3的醋酸-醋酸钠缓冲溶液作酸化体系,于70 ~80℃下酸化2~3h后用十二烷基硫酸钠(SDS)进行电位滴定,对C12-C18单长链烷基甜菜碱以及双十二烷基甜菜碱都能得到满意的结果,回收牢达到97%一102%.以硫酸作酸化剂,将pH提高到2左右,于室温下酸化lh后滴定,亦

  7. 无汞重铬酸钾-自动电位滴定法准确测定矿石中的全铁含量%Accurate Determination of Total Iron in Ores by Automatic Potentiometric Titration without Potassium Dichromate

    Institute of Scientific and Technical Information of China (English)

    赵怀颖; 温宏利; 夏月莲; 巩爱华; 马生凤

    2012-01-01

    铁矿石样品采用Na2O2碱熔进行前处理,自动电位滴定法准确测定矿石中全铁的含量.对于样品溶液Fe3+的还原方式,考察了SnCl2-HgC12、SnC12、TiC13、SnCl2-TiCl3四种方式,确定选用SnCl2-TiCl3联合还原,不仅避免了有毒试剂的使用,而且滴定终点电位突跃明显.自动电位滴定法的相对误差(RE)为0.13%,精密度(RSD)为0.22%,优于手动滴定法,避免了手动滴定受终点颜色判断误差、分析者水平等因素影响的不足.将建立的SnCl2-TiCl3-K2Cr2O7自动电位滴定法应用于6个铁含量大于30%的矿石标准物质分析,RE<0.2%,RSD<0.3%(n=10).该方法对于钒钛磁铁矿样品GBW07226a、GBW07224无需分离,可直接测定,样品分解方法简单快捷,适用性强,样品不会飞溅且分解完全,适用于需要较高准确度的铁矿石尤其是高含量铁矿石样品的分析工作.%For iron ores, this paper discusses an alkali fusion method of sodium peroxide to resolve the ores without splash and complete decomposition. Four methods of reducing Fe3+ to Fe2+ are also discussed, using stannous chloride and titanium trichloride as this not only avoids the use of toxic reagents, but also has a clearly potential jump at the end of the titration. Finally, the manual titration method is replaced by an automatic potentiometric titration to avoid manual errors, such as the judgement of the end of titration by colour and the level of experience of the analyst. The relative error can be reduced to 0. 13% and the relative standard deviation is 0. 22%. A new SnCl2 - TiCl3 - K2 Cr2 O7 automatic potentiometric titration method has been developed. It has been applied to detect six National Standard Reference iron ore samples where the content of iron is higher than 30% and the relative error is lower than 0. 2% , the relative standard deviation being lower than 0. 3% (n = l0). The magnetite GBW 07226a and GBW 07224 with high vanadium and titanium can be determined

  8. Determination on Content of Chloride in the FGD System Wastewater by Automatic Potentiometric Titration%自动电位滴定法测定湿法脱硫系统脱硫废水中氯化物

    Institute of Scientific and Technical Information of China (English)

    高姗; 郭磊; 宋晓红

    2011-01-01

    By automatic potentiometric titration,at pH=5 sourish water mixtures with total ionic strength buffer,wet de-sulfurization wastewater was determinted with titration teagen of 0.05 mo1·L-1 AgNO 3.The different concentration of chloride desulfurization wastewater samples were experienced and analyzed.Tests for recovery were made by the stan-dard addition method,and the recovery were between 95.21% and 107.46%.Tests for precision were made with different samples,and the relative standard deviation(sRSDs)were between 0.19% and 5.30%.%应用自动电位滴定法,在pH=5的总离子强度缓冲溶液存在的微酸性水溶液中,用0.05 mo1·L-1硝酸银标准溶液作为滴定剂,测定了湿法脱硫废水中氯化物含量。实验对不同浓度氯化物的脱硫废水样品分别进行了实验并加以分析。用标准加入法进行了回收率试验,结果在95.21%~107.46%之间。用不同样品进行了精密度试验,方法的相对标准偏差(n=6)在0.19%~5.30%之间。

  9. 电位滴定法测定白酒总酯的不确定度分析%Evaluation of the Uncertainty in the Determination of Total Esters Content in Liquor by Automatic Potentiometric Titration

    Institute of Scientific and Technical Information of China (English)

    刘妙芬; 邱佩丽; 丁怡; 黄秋婷; 彭程

    2012-01-01

    The uncertainty components in the determination of total esters content in liquor by potentiometric titration were analyzed and quantified according to the evaluation principles of uncertainty.The effects of measurement repeatability,sampling,preparation process of standard solution,burette and molar weight etc on the uncertainty were also investigated to establish the mathematical model of uncertainty.The combined standard measurement uncertainty of total ester content was calculated to be 0.00836 g / L and the expanded uncertainty was 0.0167g / L(k = 2).%根据测量不确定度的评定原理和方法,对电位滴定法测定白酒中总酯含量过程的不确定度分量进行分析和定量,分析了测量重复性、取样、标准滴定液的标定过程、滴定管和摩尔质量等因素对测量不确定度的影响,建立了不确定度的数学模型。计算得到总酯的合成标准不确定度为uc=0.00836 g/L,扩展不确定度为U=0.0167 g/L;k=2。

  10. Determination of Content of Calcium in Desulfurization Slury by Automatic Potentiometric Titration%自动电位滴定法测定脱硫浆液中的钙含量

    Institute of Scientific and Technical Information of China (English)

    张瑞枝

    2011-01-01

    The content of calcium in desulfurization slury was determined by automatic potentiometric titration.The proposed method was applied to the determination of calcium in various contents of 14.8~26.7 mmol/L desulfurization slury,giving values of recovery and RSD's(n =5) in the ranges of 97.60%~100.72% and 0.54%~0.99% respectively.%建立了自动电位滴定法测定脱硫浆液中钙含量的方法,即取适量浆液经适当程序处理后进行滴定。对实际样品和标准溶液的测试结果表明:不同浆液样品中,14.8~26.7 mmoL/L的加标回收率为97.60%~100.72%,相对标准偏差为0.54%~0.99%(n=5),方法操作简单、快速,自动化程度高,准确度和重复性好,适用于钙含量的常规分析。

  11. Determination of chromium content in ferrochromium alloy by automatic potentiometric titration%自动电位滴定法测定铬铁合金中的铬含量

    Institute of Scientific and Technical Information of China (English)

    赵晶晶; 宁海龙; 常健辉

    2011-01-01

    A new method based on automatic potentiometric titration was established for the determination of chromium content in ferrochromium. The precision, recovery and accuracy of the method were investigated. The RSD was 0. 07%~0. 09%, and the recovery was 100. 38%~100. 45%. The method is simple and rapid* and the results are satisfactory.%利用自动电位滴定仪,建立了铬铁合金铬含量检测的一种新方法,对方法的准确度、回收率、精密度进行了全面的分析,该方法相对标准偏差为0.07%~0.09%,回收率为100.38~100.45%,该方法操作简便、测定快速,结果令人满意,是一种简便易行的测定铬铁合金中铬含量的新方法.

  12. 自动电位滴定测定马蹄提取物中多酚类化合物%Determination of Polyphenols in Chinese Water Chestnut Extraction by Automatic Potentiometric Titration

    Institute of Scientific and Technical Information of China (English)

    汤亚芳; 黄广凤

    2016-01-01

    建立电位滴定法测定马蹄中多酚类化合物含量的定量分析方法。以高锰酸钾为氧化剂,在强酸性介质中,以没食子酸为参照,用二阶微分法确定待测样品试液的滴定终点电位,对马蹄提取物中的多酚类化合物进行自动滴定,并与可见分光光度法进行对比。方法的RSD为1.29%(n=5),平均回收率为99.34%。结果表明,本方法体系可以完成对多酚类物质的快速测定。%The automatically potentiometric titration was used to determine polyphenols in Chinese Water chestnut. The sample was tested used potassium permanganate as an oxidant in strong acid medium , gallic acid as reference, and the result was compared with the visible spectrophotometry. The RSD of method was 1.29%(n=5), and the average recovery was 99.34%. The results showed that the methodology can be completed on the rapid determination of polyphenols.

  13. Determination of Chloride in Infant Formula and Adult/Pediatric Nutritional Formula by Potentiometric Titration: Single-Laboratory Validation, First Action 2015.07.

    Science.gov (United States)

    Bolong, Wu; Fengxia, Zhang; Xiaoning, Ma; Fengjuan, Zhou; Brunelle, Sharon L

    2016-01-01

    A potentiometric method for determination of chloride was validated against AOAC Standard Method Performance Requirement (SMPR(®)) 2014.015. Ten AOAC Stakeholder Panel on Infant Formula and Adult Nutritionals (SPIFAN) matrixes, including National Institute of Standards and Technology (NIST) Standard Reference Material (SRM) 1849a, were tested in duplicate on 6 independent days. The repeatability (RSDr) ranged from 0.43 to 1.34%, and the intermediate reproducibility (RSDiR) ranged from 0.80 to 3.04%. All results for NIST SRM 1849a were within the range of the certified concentration (701 ± 17 mg/100 g). Recovery was demonstrated with two overspike levels, 50 and 100%, in the 10 SPIFAN matrixes. Samples were tested in duplicate on 3 different days, and all results were within the SMPR requirement of 95 to 105%. The LOQs of the method for powdered products and ready-to-feed or reconstituted products were 20 mg/100 g and 2.2 mg/100 mL, respectively. A wide analytical range from the LOQ to 99.5% chlorine content can be reached with an appropriate dilution factor, but in practice, the upper analytical value observed in routine matrix testing was approximately 1080 mg/100 g in skim milk powder. This is a rapid, simple, and reliable chlorine-testing method applicable to infant formula, adult nutritionals, and ingredients used in these dairy-based products, such as skim milk powder, desalted whey powder, whey protein powder, and whole milk powder. PMID:26822885

  14. Digital image-based titrations.

    Science.gov (United States)

    Gaiao, Edvaldo da Nobrega; Martins, Valdomiro Lacerda; Lyra, Wellington da Silva; de Almeida, Luciano Farias; da Silva, Edvan Cirino; Araújo, Mário César Ugulino

    2006-06-16

    The exploitation of digital images obtained from a CCD camera (WebCam) as a novel instrumental detection technique for titration is proposed for the first time. Named of digital image-based (DIB) titration, it also requires, as a traditional titration (for example, spectrophotometric, potentiometric, conductimetric), a discontinuity in titration curves where there is an end point, which is associated to the chemical equivalence condition. The monitored signal in the DIB titration is a RGB-based value that is calculated, for each digital image, by using a proposed procedure based on the red, green, and blue colour system. The DIB titration was applied to determine HCl and H3PO4 in aqueous solutions and total alkalinity in mineral and tap waters. Its results were compared to the spectrophotometric (SPEC) titration and, by applying the paired t-test, no statistic difference between the results of both methods was verified at the 95% confidence level. Identical standard deviations were obtained by both titrations in the determinations of HCl and H3PO4, with a slightly better precision for DIB titration in the determinations of total alkalinity. The DIB titration shows to be an efficient and promising tool for quantitative chemical analysis and, as it employs an inexpensive device (WebCam) as analytical detector, it offers an economically viable alternative to titrations that need instrumental detection. PMID:17723410

  15. Study on automatic potentiometric titration for the determination of free hydroxide in the straight hair cream (agent)%自动电位滴定仪连续测定直发产品中游离氢氧化物方法的研究

    Institute of Scientific and Technical Information of China (English)

    周长美; 李小娟; 吴健

    2012-01-01

    Objective: To build up a method for fast and accurate determination of free hydroxide in the straight hair products. Methods: Free hydroxide in the straight hair products reacted with the hydrochloric acid, pH combination glass electrode potential may change and automatic potentiometric titrator was used to record the titration of the hydrochloric acid standard solution at pH =9. 2, then free hydroxide content in the samples was calculated. Results : The precision of automatic potentiometric titrator method was better than manual titration, the relative standard deviation was 0. 55% ; the former also has better accuracy, the average recovery of three groups of samples was between 97. 6% and 102. 9%. It has a good effect on removing ammonia from straight hair products by vacuum. Conclusion: Automatic potentiometric titration method for the determination of free hydroxide in the straight hair cream (agent) in the samples is simple, fast and accurate, suitable for batch testing with strong practical utility.%目的:建立一种快速、准确的测定直发产品中游离氢氧化物的方法.方法:直发产品中游离氢氧化物与盐酸发生中和反应,pH复合玻璃电极上电位发生变化,在溶液pH =9.2时自动记录盐酸标准溶液的滴定量,从而计算出样品中游离氢氧化物含量.结果:自动电位滴定仪法的精密度优于人工滴定法,相对标准偏差为0.55%;方法有较好的准确度,三组样品测得的平均加标回收率为97.6% ~ 102.9%,总平均加标回收率为98.9%;方法中抽真空法去除氨效果良好.结论:运用自动电位滴定法测定直发膏(剂)类样品中的游离氢氧化物,方法简便、快速、准确,该方法适合批量检测,实用性强.

  16. An estimated potentiometric surface of the Death Valley region, Nevada and California, developed using geographic information system and automated interpolation techniques

    International Nuclear Information System (INIS)

    An estimated potentiometric surface was constructed for the Death Valley region, Nevada and California, from numerous, disparate data sets. The potentiometric surface was required for conceptualization of the ground-water flow system and for construction of a numerical model to aid in the regional characterization for the Yucca Mountain repository. Because accurate, manual extrapolation of potentiometric levels over large distances is difficult, a geographic-information-system method was developed to incorporate available data and apply hydrogeologic rules during contour construction. Altitudes of lakes, springs, and wetlands, interpreted as areas where the potentiometric surface intercepts the land surface, were combined with water levels from well data. Because interpreted ground-water recharge and discharge areas commonly coincide with groundwater basin boundaries, these areas also were used to constrain a gridding algorithm and to appropriately place local maxima and minima in the potentiometric-surface map. The resulting initial potentiometric surface was examined to define areas where the algorithm incorrectly extrapolated the potentiometric surface above the land surface. A map of low-permeability rocks overlaid on the potentiometric surface also indicated areas that required editing based on hydrogeologic reasoning. An interactive editor was used to adjust generated contours to better represent the natural water table conditions, such as large hydraulic gradients and troughs, or ''vees''. The resulting estimated potentiometric-surface map agreed well with previously constructed maps. Potentiometric-surface characteristics including potentiometric-surface mounds and depressions, surface troughs, and large hydraulic gradients were described

  17. The Study on Detection of Chloride Ion in Flue Gas Ammonium Sulfate Slurry by Automatic Potentiometric Titration Method%自动电位滴定法测定烟气氨法脱硫模拟浆液中氯离子的研究

    Institute of Scientific and Technical Information of China (English)

    杭蕾; 吕程; 陈慧慧; 连洲洋; 袁礼锐; 魏无际

    2015-01-01

    Chloride ion content of ammonia desulfurization process is an important monitoring indicators and this paper dis-cusses the detection of chloride ions in ammonium sulfate slurry by automatic potentiometric titration .The results show that :adding ethanol helps to increase the magnitude of the potential jump ;when pH=3-5 ,the result is accurate ;the recovery rate keeps between 90% and 110% ;compared with the Mohr method ,the test result is more accurate and precise and free from ash color;also the tested result is close to ion chromatography detection result ,but the high concentrations of chloride ion potentiometric titration is more advantageous .%氯离子含量是氨法脱硫工艺中的一个重要监控指标,用自动电位滴定法测定氨法脱硫浆液中的氯离子。结果表明,实验加入乙醇有利于增大电位突跃幅度;pH值为3~5时实验结果准确;加标回收率为90%~110%;与莫尔法相比,测定结果准确度、精密度更高,且不受灰分颜色干扰;与离子色谱法测定结果准确度、精密度相近,但测定高浓度氯离子电位滴定法更有优势。

  18. The determination of titratable acidity and total tannins in red wine

    OpenAIRE

    Rajković Miloš B.; Sredović Ivana D.

    2009-01-01

    Titration acidity and content of total tannins in mass-market red wines are analyzed in this paper. The content of total acids in wine, expressed through wine acid, was analyzed by potentiometric titration on 7.00 pH value. According to titratable acidity in analyzed wines, all wines (only) with analyzed parameters according to Regulations about wine quality. The analysis of differential potentiometric curves shows that these curves can give the answer to the question if non organic substance...

  19. 超声溶解-电位滴定法测定硅钢涂层用纳米二氧化钛中氯%Determination of chlorine in nanoscale titanium dioxide used in silicon steel coating by potentiometric titration with ultrasonic dissolution

    Institute of Scientific and Technical Information of China (English)

    闻向东; 谭谦; 邵梅; 张穗忠

    2015-01-01

    采用加酸后超声震荡的方法处理样品,建立了电位滴定法测定了硅钢涂层用纳米二氧化钛中氯离子含量的方法。实验确定了最佳条件:称取0.1 g过300目(50μm)筛孔的样品,加入20 mL硝酸(1+5)后,在90 kHz的条件下室温超声振荡30 min,过滤后稀释,以等体积自动加入0.10 mL 0.01 mol/L硝酸银标准滴定溶液的方式进行滴定,以d2 E/dV2-V滴定曲线中E/V的二阶倒数为零时计算滴定终点。将方法应用于硅钢涂层用纳米二氧化钛实际样品分析,结果与分光光度法一致,相对标准偏差(RSD, n=8)小于5%,加标回收率为99%~102%。%The sample was treated in acid by ultrasonic oscillation. A determination method of chlorine ion content in nanoscale titanium dioxide used in silicon steel coating was established by potentiometric titration. The optimal conditions were obtained by experiments:0. 1 g of sample was screened with 300-mesh (50μm) sieve;the sample was dissolved at room temperature with 20 mL of nitric acid (1+5) by ultrasonic oscillation at 90 kHz for 30 min;after filtration and dilution, the sample solution was titrated with 0. 10 mL of 0. 01 mol/L silver nitrate standard ti-tration solution by isovolumetric automatic addition. The titration endpoint was calculated when the second deriva-tive of E/V in d2 E/dV2-V titration curve was zero. The proposed method was applied to the analysis of actual sam-ple of nanoscale titanium dioxide used in silicon steel coating. The results were consistent with those obtained by spectrophotometry. The relative standard deviation ( RSD, n=8 ) was less than 5%, and the recoveries were be-tween 99% and 102%.

  20. Caracterização ácido-base da superfície de espécies mistas da alga Spirulina através de titulação potenciométrica e modelo de distribuição de sítios discretos Acid base characterization of the surface of mixed species of algae Spirulin by potentiometric titration and discrete site distribution model

    OpenAIRE

    Elizabete C. de Lima; Jorge C. Masini

    1999-01-01

    Acid base properties of mixed species of the microalgae Spirulina were studied by potentiometric titration in medium of 0.01 and 0.10 mols L-1 NaNO3 at 25.0±0.10 C using modified Gran functions or nonlinear regression techniques for data fitting. The discrete site distribution model was used, permitting the characterization of five classes of ionizable sites in both ionic media. This fact suggests that the chemical heterogeneity of the ionizable sites on the cell surface plays a major role on...

  1. Making pH calculations in the titration of strong protolytes

    OpenAIRE

    Milla González, Miguel

    2013-01-01

    Titration graphs of protolytic systems are very useful among other things to find the equivalence point (ep), choose the most suitable indicator, calculate the titration error and decide whether a given titration is feasible or not under certain conditions. The main feature of a titration curve is the pH jump that occurs in the vicinity of the equivalence point. Titration graphs can be obtained experimentally using the potentiometric method with the pH electrode. They also can be obtained the...

  2. Application of mensurating alkalinity in PO by automatic potentiometric titration%自动电位滴定仪在测定环氧丙烷中碱度的应用

    Institute of Scientific and Technical Information of China (English)

    庄恒榕

    2015-01-01

    采用电石渣作皂化剂的氯醇法生产环氧丙烷(PO),其碱度会对下游产品产生影响,而目前PO碱度检测无国家标准可参考。为了有效检测PO中的碱度,本文研究建立了一种自动电位滴定仪测定方法。实验结果表明,该方法的精密度和准确度符合要求,且操作简单。%At present,the normal chlorohydrination of carbide slag as saponification agent to produce the propylene oxide (denoted as PO)has a negative effect for the down-stream product,and the alkalinity of PO has not been exactly detected so far. Herein,we develop an efficient automatic potentiometric tritration method to detect the alkalinity of PO sample. In conclusion,a facile method can be employed to mensurate the alkalinity of PO,and the results are much more accurate than normal measurement method.

  3. 自动电位滴定法标定硫酸铈溶液和测定硫酸亚铁片中铁含量%Calibration of Ceric Sulfate Solution and Determination of Fe in Ferrous Sulfate Tablets by Automatic Potentiometric Titration Method

    Institute of Scientific and Technical Information of China (English)

    伍建君; 汪严; 杨孝容

    2014-01-01

    Automatic potentiometric titration method (APTM)was applied to the calibration of ceric sulfate solution and ferrum in ferrous sulfate tablets was determined by APTM.The end-point of titration was measured with potential jump by APTM.Value of RSD (n=5)found was 0.070% for calibration of ceric sulfate with sodium oxalate solution at temperatures between 45 ℃ and 50 ℃.A ferrous sulfate tablet was dissolved with 0.01 mol· L-1 sulfuric acid solution (30 mL)and titrated directly with ceric sulfate solution for determination of ferrum.The proposed method was applied in the analysis of samples of ferrous sulfate tablets,giving values of recovery of 100%and RSD′s (n=5)in the range of 1.2%-2.6%.%采用自动电位滴定法标定硫酸铈溶液,并进行硫酸亚铁片中铁含量的测定。自动电位滴定法以电位突跃监测终点,在45℃~50℃之间,以草酸钠溶液标定硫酸铈溶液,测定值的相对标准偏差(n=5)为0.070%。取硫酸亚铁片1片用0.01 mol·L-1硫酸溶液30 mL 溶解,直接用硫酸铈溶液滴定测定铁含量。方法用于硫酸亚铁片样品分析,回收率为100%,测定值的相对标准偏差(n=5)在1.2%~2.6%之间。

  4. Coupled chemical processes at clay/electrolyte interface : A batch titration study of Na-montmorillonites

    OpenAIRE

    DUC, M; F. Thomas; GABORIAUD, F

    2006-01-01

    The present work addresses the protolytic charge of montmorillonite, which occurs on the broken-bond sites at the particle edges. The purpose is to overcome the general difficulty arising in potentiometric titration due to coupled side reactions, which severely impede the titrant budget (partial dissolution of the clay and of secondary phases, hydrolysis and readsorption of dissolved species, cation exchange). Batch potentiometric titrations were carried out on the montmorillonite fractions e...

  5. Method for the Determination of Chloride Ion Flux with the Automatic Potentiometric Titration%自动电位滴定法测定焊剂中氯离子的方法

    Institute of Scientific and Technical Information of China (English)

    朵云琨; 邓勇; 朵云峰

    2014-01-01

    采用自动电位滴定法测定焊剂中氯离子的质量分数,对试样的处理、酸度的影响、线性范围、标准回收、精密度和准确度等进行探究.结果表明:对样品11次测定值的相对标准偏差(RSD)为2.27%~2.35%,标准回收率为99.00%~100.80%;所用方法的准确度和精密度较好,适合于焊剂中0.02%~1.00%氯离子的测定.%Using Auto-electric titration method measured Cl-in flux of mass fraction,the sample processing,the effects of acidity,linear range,standard recovery,precision and accuracy were studied.The results show that:the relative standard deviation of the measured val-ue of the samples for eleven times (RSD)ranged from 2.27%-2.35%;the standard recovery rate was 99.0%-100.8%;The accuracy and precision of the method are good,and suitable for the determination of 0.02%-1.00%in the flux of chloride ion.

  6. Potentiometric determination of ibuprofen, indomethacin and naproxen using an artificial neural network calibration

    Directory of Open Access Journals (Sweden)

    A. HAKAN AKTAŞ

    2008-01-01

    Full Text Available In this study, three anti-inflammatory agents, namely ibuprofen, indomethacin and naproxen, were titrated potentiometrically using tetrabutylammonium hydroxide in acetonitrile solvent under a nitrogen atmosphere at 25 °C. MATLAB 7.0 software was applied for data treatment as a multivariate calibration tool in the potentiometric titration procedure. An artificial neural network (ANN was used as a multivariate calibration tool in the potentiometric titration to model the complex non-linear relationship between ibuprofen, indomethacin and naproxen concentrations and the millivolt (mV of the solutions measured after the addition of different volumes of the titrant. The optimized network predicted the concentrations of agents in synthetic mixtures. The results showed that the employed ANN can precede the titration data with an average relative error of prediction of less than 2.30 %.

  7. Gran method for end point anticipation in monosegmented flow titration

    OpenAIRE

    Aquino Emerson V; Pasquini Celio; Rohwedder Jarbas J. R.; Raimundo Jr Ivo M.; Montenegro M. Conceição B. S. M; Araújo Alberto N

    2004-01-01

    An automatic potentiometric monosegmented flow titration procedure based on Gran linearisation approach has been developed. The controlling program can estimate the end point of the titration after the addition of three or four aliquots of titrant. Alternatively, the end point can be determined by the second derivative procedure. In this case, additional volumes of titrant are added until the vicinity of the end point and three points before and after the stoichiometric point are used for end...

  8. Study on the determination of chIoride ions in the continuous detection by muIti-project automatic potentiometric titration%多项目自动电位滴定连续检测中氯离子测定的研究

    Institute of Scientific and Technical Information of China (English)

    戴恩贤; 周英

    2015-01-01

    采用国际先进的多功能自动电位滴定仪,实现在同一杯水中自动连续检测多项水质指标,是水处理工作中先进高效的新颖检测方法。然而在同一杯水中测定多项指标,是否会彼此产生干扰,需要进行试验研究。作者为配合该方法的国家标准制订,针对多项目连续检测中氯离子测定的影响因素进行系列研究分析,确认多项目自动检测中氯离子的测定是准确可靠的。%Multiple indices of water quality can be detected in the same cup of water automatically and continuously by the international,advanced,multifunctional&automatic potentiometric titration,which is an advanced and effi-cient detection method in water treatment. However ,it needs to be tested and studied whether there will be interfer-ence when multiple indices are detected in the same cup of water. According to the influential factors of chloride ion determination in the continuous detection ,series of study and analyses have been carried out to coordinate with the formulation of national standards. It is confirmed that the determination of chloride ions in the multi-project automatic detection is accurate and reliable.

  9. Caracterização ácido-base da superfície de espécies mistas da alga Spirulina através de titulação potenciométrica e modelo de distribuição de sítios discretos Acid base characterization of the surface of mixed species of algae Spirulin by potentiometric titration and discrete site distribution model

    Directory of Open Access Journals (Sweden)

    Elizabete C. de Lima

    1999-09-01

    Full Text Available Acid base properties of mixed species of the microalgae Spirulina were studied by potentiometric titration in medium of 0.01 and 0.10 mols L-1 NaNO3 at 25.0±0.10 C using modified Gran functions or nonlinear regression techniques for data fitting. The discrete site distribution model was used, permitting the characterization of five classes of ionizable sites in both ionic media. This fact suggests that the chemical heterogeneity of the ionizable sites on the cell surface plays a major role on the acid-base properties of the suspension in comparison to electrostatic effects due to charge-charge interactions. The total of ionizable sites were 1.75±0.10 and 1.86±0.20 mmolsg-1 in ionic media of 0.01 and 0.10 mols L-1 NaNO3, respectively. A major contribution of carboxylic groups was observed with an average 34 and 22% of ionizable sites being titrated with conditional pcKa of 4.0 and 5.4, respectively. The remaining 44% of ionizable sites were divided in three classes with averaged conditional pcKa of 6.9, 8.7 and 10.12, which may be assigned respectively to imidazolic, aminic, and phenolic functionalities.

  10. Dysprosium selective potentiometric membrane sensor

    Energy Technology Data Exchange (ETDEWEB)

    Zamani, Hassan Ali, E-mail: haszamani@yahoo.com [Department of Applied Chemistry, Mashhad Branch, Islamic Azad University, Mashhad (Iran, Islamic Republic of); Faridbod, Farnoush; Ganjali, Mohammad Reza [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran (Iran, Islamic Republic of)

    2013-03-01

    A novel Dy(III) ion-selective PVC membrane sensor was made using a new synthesized organic compound, 3,4-diamino-N Prime -((pyridin-2-yl)methylene)benzohydrazide (L) as an excellent sensing element. The electrode showed a Nernstian slope of 19.8 {+-} 0.6 mV per decade in a wide concentration range of 1.0 Multiplication-Sign 10{sup -6}-1.0 Multiplication-Sign 10{sup -2} mol L{sup -1}, a detection limit of 5.5 Multiplication-Sign 10{sup -7} mol L{sup -1}, a short conditioning time, a fast response time (< 10 s), and high selectivity towards Dy(III) ion in contrast to other cations. The proposed sensor was successfully used as an indicator electrode in the potentiometric titration of Dy(III) ions with EDTA. The membrane sensor was also applied to the F{sup -} ion indirect determination of some mouth washing solutions and to the Dy{sup 3+} determination in binary mixtures. Highlights: Black-Right-Pointing-Pointer The novelty of this work is based on the high affinity of the ionophore toward the Dy{sup 3+} ions. Black-Right-Pointing-Pointer This technique is very simple, fast and inexpensive and it is not necessary to use sophisticated equipment. Black-Right-Pointing-Pointer The newly developed sensor is superior to the formerly reported Dy{sup 3+} sensors in terms of selectivity.

  11. Potentiometric sensors for the selective determination of sulbutiamine.

    Science.gov (United States)

    Ahmed, M A; Elbeshlawy, M M

    1999-11-01

    Five novel polyvinyl chloride (PVC) matrix membrane sensors for the selective determination of sulbutiamine (SBA) cation are described. These sensors are based on molybdate, tetraphenylborate, reineckate, phosphotun gestate and phosphomolybdate, as possible ion-pairing agents. These sensors display rapid near-Nernstian stable response over a relatively wide concentration range 1x10(-2)-1x10(-6) M of sulbutiamine, with calibration slopes 28 32.6 mV decade(-1) over a reasonable pH range 2-6. The proposed sensors proved to have a good selectivity for SBA over some inorganic and organic cations. The five potentiometric sensors were applied successfully in the determination of SBA in a pharmaceutical preparation (arcalion-200) using both direct potentiometry and potentiometric titration. Direct potentiometric determination of microgram quantities of SBA gave average recoveries of 99.4 and 99.3 with mean standard deviation of 0.7 and 0.3 for pure SBA and arcalion-200 formulation respectively. Potentiometric titration of milligram quantities of SBA gave average recoveries of 99.3 and 98.7% with mean standard deviation of 0.7 and 1.2 for pure SBA and arcalion-200 formulation, respectively. PMID:10703998

  12. Chemical sensors and the development of potentiometric methods for liquid media analysis

    International Nuclear Information System (INIS)

    Aspects of applying indirect potentiometric determination to chemical analysis are considered. Among them are the standard and modified addition and subtraction methods, the multiple addition method, and potentiometric titration using ion-selective electrodes as indicators. These methods significantly extend the capabilities of ion-selective potentiometric analysis. Conditions for the applicability of the above-mentioned methods to various samples (Cd, REE, Th, iodides and others) are discussed using all available ion-selective electrodes as examples. 162 refs., 2 figs., 5 tabs

  13. Permian potentiometric analysis

    International Nuclear Information System (INIS)

    Pacific Northwest Laboratory (PNL) was requested to analyze potentiometric data from the Wolfcamp Formation of the Permian System to evaluate the recommendations by the University of Texas/Bureau of Economic Geology (UT/BEG) that additional geohydrologic boreholes be drilled into the Wolfcamp. The UT/BEG recommended that two stratigraphic and two geohydrologic borings be drilled into the Permian System during FY83 and that several shallow hydrologic tests be made in the Dockum Formation. A geostatistical technique known as kriging was applied to objectively evaluate these geohydrologic borehole recommendations. The Deaf Smith County location appears to be an excellent choice for a borehole. No high quality potentiometric data are available from Deaf Smith County and a borehole location immediately upgradient from the candidate repository site is needed. Adding this borehole location to the potentiometric data base will significantly reduce field data uncertainty near the location being studied. The Swisher County location does not appear to be the best choice. High quality data values H2206 and H2360 are located immediately upgradient from the proposed repository site. The best placement of additional geohydrological boreholes in the Wolfcamp Formation depends strongly upon the proposed repository location. The variability of the potentiometric data causes estimation errors to rapidly increase away from locations of field measurements. Suggested locations for additional boreholes for the Deaf Smith investigations are in northwest Randall or central Potter Counties. Ideal borehole locations for the Swisher county studies appear to be in southeast Randall and Armstrong Counties

  14. Permian potentiometric analysis

    Energy Technology Data Exchange (ETDEWEB)

    Devary, J.L.

    1983-09-01

    Pacific Northwest Laboratory (PNL) was requested to analyze potentiometric data from the Wolfcamp Formation of the Permian System to evaluate the recommendations by the University of Texas/Bureau of Economic Geology (UT/BEG) that additional geohydrologic boreholes be drilled into the Wolfcamp. The UT/BEG recommended that two stratigraphic and two geohydrologic borings be drilled into the Permian System during FY83 and that several shallow hydrologic tests be made in the Dockum Formation. A geostatistical technique known as kriging was applied to objectively evaluate these geohydrologic borehole recommendations. The Deaf Smith County location appears to be an excellent choice for a borehole. No high quality potentiometric data are available from Deaf Smith County and a borehole location immediately upgradient from the candidate repository site is needed. Adding this borehole location to the potentiometric data base will significantly reduce field data uncertainty near the location being studied. The Swisher County location does not appear to be the best choice. High quality data values H2206 and H2360 are located immediately upgradient from the proposed repository site. The best placement of additional geohydrological boreholes in the Wolfcamp Formation depends strongly upon the proposed repository location. The variability of the potentiometric data causes estimation errors to rapidly increase away from locations of field measurements. Suggested locations for additional boreholes for the Deaf Smith investigations are in northwest Randall or central Potter Counties. Ideal borehole locations for the Swisher county studies appear to be in southeast Randall and Armstrong Counties.

  15. The first 110 years of laboratory automation: technologies, applications, and the creative scientist.

    Science.gov (United States)

    Olsen, Kevin

    2012-12-01

    Prior to the widespread availability of electronic components after the Second World War, laboratory automation was constructed by end users and designed for specific tasks, mostly filtration, percolation, and washing operations. The earliest mention of automation in the chemical literature of the United States was in 1875, announcing a device to wash filtrates unattended. In the years that followed, a small number of commercial automated devices were sold, including large grinders for the preparation of coal samples. Around 1900, power stations began adopting automated carbon dioxide analysis. The development of electrical equipment for conductivity measurements enabled the first commercial, automated gas detection instruments for laboratory and field use around the time of the First World War. The growth of industrial production in the 1920s led to a desire for automated testing equipment, and the growing rubber industry was among the more successful early adapters. Photoelectric cells were first used in the early 1930s to create automatic titrators, and by the 1950s, automatic titration encompassed coulometric, potentiometric, and photometric devices. Combinations of chart recorders, photocells, and timers created other types of automated equipment such as stills and fraction collectors. The first true stand-alone automation for the laboratory included clinical chemistry analyzers, introduced during the 1950s. PMID:22893633

  16. Automated oxygen titration and weaning with FreeO2 in patients with acute exacerbation of COPD: a pilot randomized trial

    Directory of Open Access Journals (Sweden)

    Lellouche F

    2016-08-01

    Full Text Available François Lellouche,1 Pierre-Alexandre Bouchard,1 Maude Roberge,1 Serge Simard,1,2 Erwan L’Her,1,3 François Maltais,1 Yves Lacasse1 1Research Centre, 2Biostatistics Department, Quebec Heart and Lung Institute, Laval University, 3Emergency Medicine, Hôtel-Dieu de Lévis, Laval University, Quebec City, QC, Canada Introduction: We developed a device (FreeO2 that automatically adjusts the oxygen flow rates based on patients’ needs, in order to limit hyperoxia and hypoxemia and to automatically wean them from oxygen. Objective: The aim of this study was to evaluate the feasibility of using FreeO2 in patients hospitalized in the respiratory ward for an acute exacerbation of COPD. Methods: We conducted a randomized controlled trial comparing FreeO2 vs manual oxygen titration in the respiratory ward of a university hospital. We measured the perception of appropriateness of oxygen titration and monitoring in both groups by nurses and attending physicians using a Likert scale. We evaluated the time in the target range of oxygen saturation (SpO2 as defined for each patient by the attending physician, the time with severe desaturation (SpO2 <85%, and the time with hyperoxia (SpO2 >5% above the target. We also recorded length of stay, intensive care unit admissions, and readmission rate. Fifty patients were randomized (25 patients in both groups; mean age: 72±8 years; mean forced expiratory volume in 1 second: 1.00±0.49 L; and mean initial O2 flow 2.0±1.0 L/min. Results: Nurses and attending physicians felt that oxygen titration and monitoring were equally appropriate with both O2 administration systems. The percentage of time within the SpO2 target was significantly higher with FreeO2, and the time with severe desaturation and hyperoxia was significantly reduced with FreeO2. Time from study inclusion to hospital discharge was 5.8±4.4 days with FreeO2 and 8.4±6.0 days with usual oxygen administration (P=0.051. Conclusion: FreeO2 was deemed as an

  17. Multi-task flow system for potentiometric analysis: its application to the determination of vitamin B6 in pharmaceuticals.

    Science.gov (United States)

    Fernandes, R N; Sales, M G; Reis, B F; Zagatto, E A; Araújo, A N; Montenegro, M C

    2001-07-01

    A flow set-up based on the sequential injection analysis concept was designed, aiming at increased automation and robustness of procedures related with potentiometric detection in pharmaceutical control. In this sense, programmable set-up calibration, ion-selective electrode characterization, standard addition techniques and titration procedures could be carried out without any stock solutions conventional handling or modification on the physical structure of the flow system. Evaluation of a flow-through vitamin B6 selective electrode and its application to routine analysis of pharmaceuticals were selected as models to demonstrate the system potentialities. The system ability to generate in-line calibrating solutions was verified by comparing the results with those obtained with solutions prepared by the manual procedure. The vitamin B6 determination in pharmaceutical products was carried out and in-line performed recoveries gave values within 97.4-103.5%. The system ability to perform titrations was ascertained using the precipitation reaction of vitamin B6 with tetraphenylborate. Other profitable features such as lower reagent consumption with a low effluent generation volume were also achieved. PMID:11377053

  18. Polyelectrolyte assisted charge titration spectrometry: applications to latex and oxide nanoparticles

    OpenAIRE

    Mousseau, F.; Vitorazi, L.; Herrmann, L.; S Mornet; Berret, J. -F.

    2016-01-01

    The electrostatic charge density of particles is of paramount importance for the control of the dispersion stability. Conventional methods use potentiometric, conductometric or turbidity titration but require large amount of samples. Here we report a simple and cost-effective method called polyelectrolyte assisted charge titration spectrometry or PACTS. The technique takes advantage of the propensity of oppositely charged polymers and particles to assemble upon mixing, leading to aggregation ...

  19. Potentiometric determination of hexavalent uranium in uranium silicide samples

    International Nuclear Information System (INIS)

    The Chilean Nuclear Energy Commission's Department of Nuclear Materials has among its projects the production of fuels elements for nuclear reactors, and, therefore, the Chemical Analysis Laboratory must have a rapid and reliable method for uranium analysis, to control the uranium concentration during each stage of the production process. For this reason the Chilean Nuclear Energy Commission's Chemical Analysis Laboratory has validated a potentiometric method, which is a modification of the Davies and Gray method proposed by A.R. Eberle. This method uses the Potentiometric Titration Technique and is based on the direct and rapid reduction of uranium (VI) to Uranium (IV), in a concentrated phosphoric acid medium, with excess iron (II) used as a reducing agent. In this medium the excess iron (II) selectively oxidizes to iron (III) with nitric acid, using molybdenum (IV) as a catalyzer, the nitrous acid that is produced is eliminated by adding amidosulfuric acid. The solution is diluted with 1M sulfuric acid and the uranium (IV) obtained is titrated potentiometrically with potassium dichromate in the presence of vanadilic sulfate to obtain a better defined final titration point. The samples were softened with hydrochloric acid and nitric acid and later 50 ml were estimated in a 20% sulfuric acid medium. The analytical method was validated by comparing it with Certified Reference Material (C.R.M.) from the New Brunswick Laboratory (NBL), Metallic Uranium, CRM 112-A. The F Test and the T Test show that the value calculated is less than the tabulated value so the result is traceable to the reference material. The quantification limit, sensitivity, precision and accuracy were quantified for the method

  20. Plutonium potentiometric analysis after reduction by copper (I)

    International Nuclear Information System (INIS)

    Plutonium determination in solutions containing fission products and an important amount of uranium (ratio U/Pu = 7), suitable for a mass of plutonium between 5 to 30 mg, by reduction of plutonium to the valency state III with an excess of copper (I) in hydrochloric acid saturated with aluminium chloride and sulfamic acid; molybdemum (VI) and uranium (VI) are not reduced. Copper (I) in excess is titrated potentiometrically with potassium dichromate. Addition of sulfuric-phosphoric acid and oxidation of plutonium to the valency state IV by potassium dichromate by potentiometry. The mass of plutonium is obtained from the volume of dichromate used

  1. The Davies-Gray titration for the assay of uranium in nuclear materials: a performance study

    International Nuclear Information System (INIS)

    An interlaboratory comparison in two phases was organized to assess the precision and accuracy concerning the assay of uranium in nuclear materials by the potentiometric titration method. This contribution presents the results of this exercise in terms of method performance. Variations to be expected between different laboratories and within a single laboratory are estimated. In general, the method proved again very reliable. (orig.)

  2. Titulação potenciométrica aplicada na determinação de ácidos graxos livres de óleos e gorduras comestíveis Potentiometric titration applied to free fatty acid determination of edible oils and fats

    OpenAIRE

    Cibele Cristina Osawa; Lireny Ap. Guaraldo Gonçalves; Sidnei Ragazzi

    2006-01-01

    Free fatty acids are a measure of evaluating fats and oils, submitted to abusive conditions, besides being a quality characteristic of edible vegetable oils. The official method of determination (AOCS Ca 5a-40, 2004) is based on titration, using phenolphthalein as an indicator. For crude and degummed oils, the titration end point is difficult to be observed due to the high level of pigments, resulting in dark solutions. In this case and others, such as self-life studies, in which sample quant...

  3. Surfactant/detergent titration analysis method and apparatus for machine working fluids, surfactant-containing wastewater and the like

    Science.gov (United States)

    Smith, D.D.; Hiller, J.M.

    1998-02-24

    The present invention is an improved method and related apparatus for quantitatively analyzing machine working fluids and other aqueous compositions such as wastewater which contain various mixtures of cationic, neutral, and/or anionic surfactants, soluble soaps, and the like. The method utilizes a single-phase, non-aqueous, reactive titration composition containing water insoluble bismuth nitrate dissolved in glycerol for the titration reactant. The chemical reaction of the bismuth ion and glycerol with the surfactant in the test solutions results in formation of micelles, changes in micelle size, and the formation of insoluble bismuth soaps. These soaps are quantified by physical and chemical changes in the aqueous test solution. Both classical potentiometric analysis and turbidity measurements have been used as sensing techniques to determine the quantity of surfactant present in test solutions. This method is amenable to the analysis of various types of new, in-use, dirty or decomposed surfactants and detergents. It is a quick and efficient method utilizing a single-phase reaction without needing a separate extraction from the aqueous solution. It is adaptable to automated control with simple and reliable sensing methods. The method is applicable to a variety of compositions with concentrations from about 1% to about 10% weight. It is also applicable to the analysis of waste water containing surfactants with appropriate pre-treatments for concentration. 1 fig.

  4. Using Spectrophotometric Titrations To Characterize Humic Acid Reactivity at Environmental Concentrations

    International Nuclear Information System (INIS)

    Potentiometric titration is a common method to characterize dissolved organic matter (DOM) reactivity. Because of the sensitivity of pH electrodes, it is necessary to work with very high DOM (≥1 g/L) concentrations that are unrealistic compared to those found in natural waters (0. 1 to 100 mg/L). To obtain proton binding data for concentrations closer to environmental values, spectroscopic titration methodology is a viable alternative to traditional potentiometric titrations. Spectrophotometric titrations and UV visible spectra of a diluted solution of purified Aldrich humic acid (5 mg(DOC)/L) are used to estimate changes in proton binding moieties as function of pH and ionic strength after calculation of differential absorbance spectra variations. After electrostatic correction of spectrophotometric data, there is a linear operational correlation between spectrophotometric and potentiometric data which can be used as a transfer function between the two properties. Spectrophotometric titrations are then used to determine the changes of humic acid protonation after adsorption onto alpha-alumina. (authors)

  5. Potentiometric end point detection in the EDTA titrimetric determination of gallium

    International Nuclear Information System (INIS)

    Gallium is titrated in presence of known amount of Fe (III) with EDTA in HNO3 solution at pH 2 to 3. The end point is detected potentiometrically employing a bright platinum wire - saturated calomel (SCE) reference electrode system, the redox couple being Fe (III) / Fe (II). Since Fe (III) is also titrated by EDTA, it is, therefore, subtracted from titre value to get the EDTA equivalent to gallium only. Precision and accuracy 0.2 to 0.4% was obtained in the results of gallium in the range of 8 to 2 mg. (author)

  6. Determination of total iron in iron ore by potentiometric titration with ascorbic acid as reducing titrant%以抗坏血酸作还原滴定剂电位滴定法测定铁矿石中全铁

    Institute of Scientific and Technical Information of China (English)

    戚淑芳; 张杰; 王莹; 宁松

    2011-01-01

    提出了以抗坏血酸作为还原滴定剂、全自动电位滴定仪判定滴定终点的测定铁矿石中全铁的方法.对滴定酸介质和酸度、温度、电位滴定仪参数进行了优化,对干扰元素的影响等进行了试验.结果表明,全铁可在铁矿石溶样的酸介质及酸度下滴定,无需进行酸度调节,滴定的温度范围为50~80℃.采用过氧化氢或过硫酸铵作预氧化剂,过量的预氧化剂煮沸数分钟即可除去,操作简便.铁矿石中大多数元素均不干扰测定,尤其是铜、钼、钒的允许量可达到5%(质量分数).测定结果相对标准偏差(RSD)小于0.2%.对两个铁矿石标准样品进行加标回收试验,得到加标回收率分别为99.6%和100.4%.%The determination method of total iron in iron ore using ascorbic acid as reducing titrant was development. The end point of titration was determined by full-automatic potential titrimeter. The titration acid medium and acidity, temperature, and potential titrimeter parameters were optimized.The influence of interference elements was tested. The results showed that titration of total iron could be carred out in the medium and acidity of dissolving iron ore samples without pH adjustment. The titration temperature range was 50 -80 ℃ . The hydrogen peroxide or ammonium persulfate was used as pre-oxidant. Since the excessive pre-oxidant could be removed by boiling for a few minutes, the operation was easy. The majority elements in iron ores did not intcrfcrc in the determination, especially the tolerant amount of copper, molybdenum and vanadium could be up to 5 % (mass fraction). The relative standard deviation (RSD) of determination results was less than 0. 2 % , and the recoveries for two samples were 99. 6% and 100. 4 % ,respectively.

  7. ''Titration'' polymerization of monovinylacetylene

    NARCIS (Netherlands)

    Mavinkurve, A; Visser, S; vandenBroek, W; Pennings, AJ

    1996-01-01

    A polymer consisting of a saturated carbon backbone with pendent acetylenic groups was prepared from monovinylacetylene. A titration was performed between the monomer and tertiary butyllithium, its lithiating agent. The charge transfer complex formed between the solvent THF and the tertiary butyllit

  8. NBL-Davies-Gray weight titration method

    International Nuclear Information System (INIS)

    The titration method for uranium consists of the following basic steps: reduction of U+6 to U+4 by Fe+2; selective oxidation of excess Fe+2 by HNO3 with Mo+6 catalyst, all in strong phosphoric acid solution; and titration of the U+4 with standard dichromate after dilution. In this paper, detailed procedure of the NBL method, its modification to a gravimetric system or weight titration technique, and miniaturization of the NBL titrimetric method are discussed. Improved precisions and accuracy (2 to 3 times), of the gravimetric titrant delivery has made it possible to reduce the amount of uranium taken for each analysis. At present, using gravimetric delivery, most samples are titrated in the 30 to 50 mg range. Improved precision has led to investigating the possibility of a scaled-down version of the basic method so as to reduce the volume of phosphoric acid waste generated. Because all reactions are carried out in the same vessel, this method can be automated. Analysts at NBL have been able to restrict error to 0.05% or better in the 30 to 100 mg range using the basic procedure

  9. Automated Methods Of Corrosion Measurements

    DEFF Research Database (Denmark)

    Bech-Nielsen, Gregers; Andersen, Jens Enevold Thaulov; Reeve, John Ch;

    1997-01-01

    The chapter describes the following automated measurements: Corrosion Measurements by Titration, Imaging Corrosion by Scanning Probe Microscopy, Critical Pitting Temperature and Application of the Electrochemical Hydrogen Permeation Cell.......The chapter describes the following automated measurements: Corrosion Measurements by Titration, Imaging Corrosion by Scanning Probe Microscopy, Critical Pitting Temperature and Application of the Electrochemical Hydrogen Permeation Cell....

  10. 滴定分析在聚酰胺合成中的应用%The Application of Titration Analysis in Synthesis of Polyamide

    Institute of Scientific and Technical Information of China (English)

    蒋莹

    2012-01-01

    The analysis methods of the amine values of potentiometric titration were introduced emphasis, titration were discussed. and acid values of polyamide were provided. The application and the accuracy and influencing factors of potentiometric%总结了聚酰胺的酸值、胺值的分析方法。重点介绍了电位滴定法的应用。讨论了电位滴定法的精确度及其影响因素。

  11. DETERMINATION OF ACID–BASE PROPERTIES OF HCL ACID ACTIVATED PALYGORSKITE BY POTENTIOMETRIE TITRATION

    OpenAIRE

    N. FriniSrasra; Srasra, E.

    2008-01-01

    The surface acidity of raw and acid activated palygorskite clay were studied by acid-base potentiometric titration. The Gran plot method was applied for the hydroxide titration and the total surface site (Hs) and the average number of protons reacted per surface site (Z) of palygorskite samples at a given ionic strength were calculated. Acid treatment increases the clay acidity and modifies its surface charge. The point of zero charge value, determined by the common crossing point of Z vs pH ...

  12. A new potentiometric determination of hydrazine in the presence of uranium(IV)

    International Nuclear Information System (INIS)

    The present method describes the determination of hydrazine by making use of potentiometric titration technique. The underlying principle is back titration of unreacted excess cerium remaining after the complete oxidation of hydrazine. Standardized ferrous ammonium sulfate was used for titration. This method was applied to 'real samples' generated from a nuclear reprocessing plant wherein control of hydrazine is of paramount importance. The interference of U(IV), Cr(III), U(VI), nitrite, and chloride was studied and of all these ions the way to eliminate the interference of U(IV) was only attempted. The relative standard deviations (RSD) for synthetic as well as 'real samples' were determined. The method gives RSD of less than 1% in the range of 1 mg to 20 mg of hydrazine. The error in the range 3 mg to 17 mg was found to be less than 1%. (author). 5 refs., 3 tabs

  13. 自动电位滴定法测定工业铬酸酐中氯离子含量方法研究%The Research Method to Determine Chloride Ion Content in Chromium Trioxide for Industrial Use with Automatic Potentiometric Titration

    Institute of Scientific and Technical Information of China (English)

    胡清启; 孙宁

    2015-01-01

    用乙醇作还原剂,将铬酸酐中CrO42-还原为Cr3+,再用硝酸银标准溶液滴定,以电位变化率最大点确定反应终点,求出氯离子含量。就精密度和加标回收进行实验,并对方法展开分析与讨论,该方法的建立对工业生产铬酸酐中氯离子指标的控制具有指导意义。%Reduce the CrO42+to Cr3+in chromium trioxide with ethanol as the reductant ,then determine the content of chloride ion using AgNO3 standard solution to titrate to the end point that has a biggest change of potential. Conduct an experiment for calculating the precision and standard addition recovery of the method,and then analysis and discuss about the method.This method has a guiding significance for controlling the content of chloride ion in the industrial production of chromium trioxide.

  14. The application of hydrogen-palladium electrode for potentiometric acid-base determinations in tetrahydrofuran

    Directory of Open Access Journals (Sweden)

    Jokić Anja B.

    2013-01-01

    Full Text Available The application of the hydrogen-palladium electrode (H2/Pd as the indicator electrode for the determination of relative acidity scale (Es, mV of tetrahydrofuran (THF and the potentiometric titrations of acids in this solvent was investigated. The relative acidity scale tetrahydrofuran was determined from the difference half-neutralization potentials of perchloric acid and tetrabutylammonium hydroxide (TBAH, which were measured by using both H2/Pd-SCE and glass-SCE electrode pairs. The experimentally obtained value of Es scale THF with a H2/Pd-SCE electrode pair was 1155 mV, and those obtained with glass-SCE electrode pair 880 mV. By using a H2/Pd indicator electrode, the individual acids (benzoic acid, palmitic acid, maleic acid, acetyl acetone, α-naphthol and two component acid mixtures (benzoic acid + α-naphthol, palmitic acid + α-naphthol, maleic acid + α-naphthol and maleic acid + ftalic acid were titrated with a standard solution of TBAH. In addition, sodium methylate and potassium hydroxide proved to be very suitable titrating agents for titrating of the individual acids and the acids in mixtures, respectively. The relative error of the determination of acids in mixture was less than 3%. The results are in agreement with those obtained by a conventional glass electrode. The advantages of H2/Pd electrode over a glass electrode in potentiometric acid-base determinations in tetrahydrofuran lie in the following: this electrode gives wider relative acidity scale THF, higher the potential jumps at the titration end-point and relatively fast response time; furthermore, it is very durable, simple to prepare and can be used in the titrations of small volumes. [Projekat Ministarstva nauke Republike Srbije, br.172051

  15. Potentiometric application of boron- and phosphorus-doped glassy carbon electrodes

    Directory of Open Access Journals (Sweden)

    ZORAN V. LAUSEVIC

    2001-03-01

    Full Text Available Acomparative study was carried out of the potentiometric application of boronand phosphorus-doped and undoped glassy carbon samples prepared at the same heat treatment temperature (HTT 1000°C. The electrochemical activities of the obtained electrode materials were investigated on the example of argentometric titrations. It was found that the electrochemical behaviour of the doped glassy carbon samples are very similar to a Sigri (undoped glassy carbon sample (HTT 2400°C. The experiments showed that the potentiometric response depends on the polarization mode, the nature of the sample, the pretreatment of the electrode surface, and the nature of the supporting electrolyte. The amounts of iodide, bromide, and of chloridewere determined to be 1.27 mg, 0.80 mg and 0.54 mg, respectively, with a maximum relative standard deviation of less than 1.1%. The obtained results are in good agreement with the results of comparative potentiometric titrations using a silver indicator electrode. The titrationmethod was applied to the indirect determination of pyridoxine hydrochloride, i.e., vitamin B6.

  16. Potentiometric studies on the complexes of tetracycline (TC) and oxytetracycline (OTC) with some metal ions

    International Nuclear Information System (INIS)

    The interaction of Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Zn(II), Cd(II), Hg(II), Pb(II), Al(III), and UO2(II) ions with tetracycline (TC) were studied by potentiometric pH titrations. The formation constants of the different binary complexes formed in such systems have been determined at 25±0.1 deg C and μ=0.1 moll-1 (NaNO3). Potentiometric pH equilibrium measurements have been made under the same conditions for the interaction of oxytetracycline (OTC) and Cu(II), Cd(II), Pb(II), and UO2(II). The formation of (1:1) binary complexes are inferred from the potentiometric pH titration curves. The protonation constants of TC and OTC were also determined under the same conditions and refined (ESAB2M computer program). The transition metal stability constants are consistent with the Irving-Williams series. (authors)

  17. PK7300全自动血型分析仪测定ABO血型抗体效价的初步研究%A preliminary study on ABO blood type antibody titration by PK7300 automated blood typing analyzer

    Institute of Scientific and Technical Information of China (English)

    石绍川; 刘东; 李军; 田耘博; 陈鹏

    2014-01-01

    目的:探索使用PK7300全自动血型分析仪测定ABO血型抗体效价的方法,探讨献血者血型检测中与ABO血型抗体效价相关的影响因素及注意事项。方法仪器微板法测定抽样标本的ABO血型抗体效价;仪器微板法及手工试管法测定各血型混合血浆的ABO血型抗体效价;统计分析该中心2013年5~7月检测出的ABO血型抗体效价降低的情况。结果A型献血者与B型献血者的ABO血型抗体效价比较,差异无统计学意义(P>0.05),O型献血者的ABO血型抗体效价明显高于A型或B型献血者(P<0.05);手工试管法的灵敏度明显优于仪器微板法,而手工试管法二的灵敏度又明显优于手工试管法一(P<0.05);ABO血型抗体效价降低的A型献血者明显多于B型或O型(均P<0.01),ABO血型抗体效价降低的男性献血者明显多于女性(P<0.01)。结论仪器微板法测定ABO血型抗体效价操作简便、结果判读客观、重复性好,1∶1~1∶80的稀释比例范围能满足绝大多数标本的测定需要,采用梯度稀释有助于减小测定误差;血型、性别、年龄、亚型等因素可能与献血者ABO血型抗体效价降低相关。%Objective To explore the detection method of ABO blood type antibody titration by the PK7300 automated blood typing analyzer and to investigate the ABO blood type antibody titer‐related influencing factors and the matter needing attentions in blood typing test for blood donors .Methods The ABO blood type antibody titers of the samples were measured by the analyzer microplate method;the ABO blood type antibody titer of each mixed plas‐ma was respectively measured by the analyzer microplate method and by the manual tube method;the decrease situa‐tion of ABO blood type antibody titers detected in our center from May to July 2013 were statistically analyzed .Re‐sults There was no statistically significant difference in the ABO

  18. Design and fabrication of a miniaturization micro volume auto titrator coupled with electrochemical end-point detector for the determination of acidity of some fruit juice

    OpenAIRE

    Prinya Masawat

    2008-01-01

    A miniaturization micro volume auto titrator coupled with electrochemical end-point detector was designed and fabricated for the determination of acidity of some Thai citrus fruit juices collected in the northern area of Thailand. The method was based on on-line potentiometric titration of the acid contents with sodium hydroxide. Conditions such as volume of fruit juice sample, volume and concentration of potassium chloride used as supporting electrolyte and flow rate of titrant were optimize...

  19. Isothermal Titration Calorimetry Can Provide Critical Thinking Opportunities

    Science.gov (United States)

    Moore, Dale E.; Goode, David R.; Seney, Caryn S.; Boatwright, Jennifer M.

    2016-01-01

    College chemistry faculties might not have considered including isothermal titration calorimetry (ITC) in their majors' curriculum because experimental data from this instrumental method are often analyzed via automation (software). However, the software-based data analysis can be replaced with a spreadsheet-based analysis that is readily…

  20. Physico chemical studies on the composition of complex arsenites of metals Part IV: conductometric and potentiometric studies on the composition of cadmium arsenite

    Directory of Open Access Journals (Sweden)

    M. S. Bhadraver

    1962-07-01

    Full Text Available The formation and precipitation of cadmium arsenite has been studied by conductometric and potentiometric titrations between cadmium nitrate and sodium arsenite (meta at different concentrations with either of the substances used as the reagent in titration. In the case of direct titrations (cadmium nitrate added to sodium arsenite in the conductivity cell, one distinct break in the curves is observed corresponding to the formation of the Cd (AsO/sub 2//sub 2/ where the molecular ratio is 2:1. The direct and reverse potentiometric titrations curves give one maxima in dE/dV at point corresponding to the formation of the complex Cd (AsO/sub/2/sub/2 where the molecular ratio of reactants Cd:AsO/sub/2 is 1:2. The composition has been arrived at by comparing the calculated values with observed values by conductometric and potentiometric titrations. The composition of cadmium arsenite arrived at both by conductometry and potentiometry is best representative as Cd(AsO/sub/2/sub/2

  1. Spectroscopic study on variations in illite surface properties after acid-base titration

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    FT-IR, Raman microscopy, XRD, 29 Si and 27 Al MAS NMR, were used to investigate changes in surface properties of a natural illitesample after acid-base potentiometric titration. The characteristic XRD lines indicated the presence of surface Al-Si complexes, preferable to Al(OH)3 precipitates. In the microscopic Raman spectra, the vibration peaks of Si-O and Al-O bonds diminished as a result of treatment withacid, then increased after hydroxide back titration. The varied ratio of signal intensity between Ⅳ Al and Ⅵ At species in 27 Al MAS NMRspectra, together with the stable BET surface area after acidimetric titration, suggested that edge faces and basal planes in the layer structure ofillite participated in dissolution of structural components. The combined spectroscopic evidence demonstrated that the reactions between illitesurfaces and acid-leaching silicic acid and aluminum ions should be considered in the model description of surface acid-base properties of theaqueous illite.

  2. Determination of the protonation enthalpy of humic acid by calorimetric titration technique

    International Nuclear Information System (INIS)

    Graphical abstract: The thermodynamic quantities of protonation of humic acid were determined by the combination of potentiometric titration and calorimetric titration. It was observed that the protonation enthalpy and Gibbs free energy had been affected by pH of solution. As a result, the thermodynamics of the protonation reaction of humic acid is influenced by the polyelectrolyte effect and the heterogeneity. - Highlights: • We applied calorimetric titration technique to the protonation of humic acid. • The thermodynamic quantities of protonation of humic acid were determined. • The protonation enthalpy of humic acid is affected by the heterogeneity. • Gibbs free energy of the protonation is affected by the polyelectrolyte effect. - Abstract: In this study, the calorimetric titration technique was used to determine the protonation enthalpy of two reference humic acids and polyacrylic acid. First, we obtained the apparent protonation constant of two kinds of humic acid purchased from IHSS (International Humic Substances Society) and polyacrylic acid by potentiometric titration. Second, we obtained the protonation enthalpy of them by calorimetric titration. The protonation enthalpy of humic acid was affected by pH and the ionic strength of bulk solution. From the comparison of ΔH between humic acid and polyacrylic acid, it was concluded that the pH dependence of ΔH is attributed to the heterogeneity of humic acid. And ΔH of phenolic hydroxyl group in humic acid is strongly influenced by the electric double layer of humic acid’s surface. This is considered to be a reason of the ionic strength dependence of ΔH. On the other hand, Gibbs free energy of the protonation of humic acid is affected by the electrostatic attraction with the progress of dissociation of functional groups such as carboxyl group and phenolic hydroxyl group. Consequently, the thermodynamics of the protonation of humic acid is affected by the polyelectrolyte effect and the

  3. Tracer-monitored flow titrations.

    Science.gov (United States)

    Sasaki, Milton K; Rocha, Diogo L; Rocha, Fábio R P; Zagatto, Elias A G

    2016-01-01

    The feasibility of implementing tracer-monitored titrations in a flow system is demonstrated. A dye tracer is used to estimate the instant sample and titrant volumetric fractions without the need for volume, mass or peak width measurements. The approach was applied to spectrophotometric flow titrations involving variations of sample and titrant flow-rates (i.e. triangle programmed technique) or concentration gradients established along the sample zone (i.e. flow injection system). Both strategies required simultaneous monitoring of two absorbing species, namely the titration indicator and the dye tracer. Mixing conditions were improved by placing a chamber with mechanical stirring in the analytical path aiming at to minimize diffusional effects. Unlike most of flow-based titrations, the innovation is considered as a true titration, as it does not require a calibration curve thus complying with IUPAC definition. As an application, acidity evaluation in vinegars involving titration with sodium hydroxide was selected. Phenolphthalein and brilliant blue FCF were used as indicator and dye tracer, respectively. Effects of sample volume, titrand/titrant concentrations and flow rates were investigated aiming at improved accuracy and precision. Results were reliable and in agreement with those obtained by a reference titration procedure. PMID:26703261

  4. 手动滴定测定甲醛方法的改进%Improving of the Method of Formaldehyde Manual Titration

    Institute of Scientific and Technical Information of China (English)

    崔永乐

    2014-01-01

    The formaldehyde content analysis is very frequent in POM production . But there are more shortcomings in the formaldehyde manual titration . After the manual titration is substituted by the automatic potentiometric titration ,the analysis requirements can be met .%在聚甲醛的生产过程中,甲醛分析的频率很高,手动滴定存在局限性,改用自动电位滴定法,可满足分析要求。

  5. Host-Tailored Sensors for Leucomalachite Green Potentiometric Measurements

    Directory of Open Access Journals (Sweden)

    F. T. C. Moreira

    2013-01-01

    Full Text Available A new biomimetic sensor for leucomalachite green host-guest interactions and potentiometric transduction is presented. The artificial host was imprinted in methacrylic acid or acrylamido-2-methyl-1-propanesulfonic acid-based polymers. Molecularly imprinted particles were dispersed in 2-nitrophenyloctyl ether and trapped in poly(vinyl chloride. The potentiometric sensors exhibited a near-Nernstian response in steady state evaluations, with slopes and detection limits ranging from 45.8 to 81.2 mV decade-1 and 0.28 to 1.01 μg mL-1, respectively. They were independent from the pH of test solutions within 3 to 5. Good selectivity was observed towards drugs that may contaminate water near fish cultures, such as oxycycline, doxycycline, enrofloxacin, trimethoprim, creatinine, chloramphenicol, and dopamine. The sensors were successfully applied to field monitoring of leucomalachite green in river samples. The method offered the advantages of simplicity, accuracy, applicability to colored and turbid samples, and automation feasibility.

  6. Potentiometric determination of trace amounts of volatile thiols in natural gas

    International Nuclear Information System (INIS)

    A potentiometric titration method was developed for the determination of volatile thiols in natural gas. An apparatus was devised for the quantitative absorption of volatile thiols. The measurements were performed in an ethanolic ammonium buffer solution containing a known amount of silver nitrate as supporting electrolyte. The excess silver was precipitated by a known amount of potassium iodide. The excess of iodide was back titrated potentiometrically with a standard solution of silver nitrate. The direct titration of the excess silver ions with a standard solution of potassium iodide gave a poor accuracy compared with the back titration method. Iodide selective electrode was employed as an indicator electrode and a silver-silver chloride electrode as reference electrode. The accuracy and reproducibility of the method were established by preparing several synthetic samples in which ethanthiol containing from 346.61 to 12.11 μUg mercaptan sulfur was taken as standard nitrogen as carrier gas with an optimum flow rate of 31.5 L/hr. The results obtained expressed in the form of Grans plot showed an error ranging from 0.16 to 2.39% by weight and the relative standard deviation did not exceed 2.20%. The amount of mercaptan sulfur determined in Iraqi natural gas taken directly in a cylinder from Dora refinery, Baghdad, Iraq, and after six months of storage we 23.15 Ug/L and 21.25 Ug/L respectively with a relative standard deviation not exceeded 1%. The interferences of hydrogen sulfide could be eliminated by absorption in cadimium acetate containing solution. Other sulfur containing compounds e.g. disulfides, sulfoxides which may be present in natural gas do not interfere with the analysis

  7. The determination of titratable acidity and total tannins in red wine

    Directory of Open Access Journals (Sweden)

    Rajković Miloš B.

    2009-01-01

    Full Text Available Titration acidity and content of total tannins in mass-market red wines are analyzed in this paper. The content of total acids in wine, expressed through wine acid, was analyzed by potentiometric titration on 7.00 pH value. According to titratable acidity in analyzed wines, all wines (only with analyzed parameters according to Regulations about wine quality. The analysis of differential potentiometric curves shows that these curves can give the answer to the question if non organic substances, amino groups and phenols are present in wine in large quantity, as they are always present in wine. However it doesn't give the clear answer which substances are present in analyzed samples. The answer to this question can be received only by the method of ionic chromatography. The content of total tannins shows short time of storage in wine cellars so wine wasn't stored long enough, i.e. they are commercial wines made for mass market production and consumption. Although they have less content of total tannin materials of given values, wine taste gives the correlation with other polyphenol materials that only give odour, aroma and 'bouquet' to wine. The relative error of mean value is very low which indicates the reproduction of results and reliability of the method of determination of total tannins in red wine.

  8. Determination of concentration of anionic and amphoteric surfactants in shampoos using potentiometric titration method

    OpenAIRE

    Saman Ahmad Nasrollahi; Hesam Alibakhshi; Alireza Firooz

    2013-01-01

    Background and Aim: Shampoos are surfactant systems to clean hair and body. Two kinds of surfactants are generally used in shampoo formulations: anionic and amphoteric. These agents, especially anionic ones may cause skin irritation and dryness after bathing. So, using a simple and fast method to determine the types and concentrations of surfactants can help to choose a product with high efficacy and low side effects. This study was aimed to determine surfactant concentrations using potentiom...

  9. Automatic set-point titration for monitoring nitrification in SBRs.

    Science.gov (United States)

    Fiocchi, N; Ficara, E; Bonelli, S; Canziani, R; Ciappelloni, F; Mariani, S; Pirani, M; Ratini, P; Mazouni, D; Harmand, J

    2008-01-01

    Nitrification is usually the bottleneck of biological nitrogen removal processes. In SBRs systems, it is not often enough to monitor dissolved oxygen, pH and ORP to spot problems which may occur in nitrification processes. Therefore, automated supervision systems should be designed to include the possibility of monitoring the activity of nitrifying populations. Though the applicability of set-point titration for monitoring biological processes has been widely demonstrated in the literature, the possibility of an automated procedure is still at its early stage of industrial development. In this work, the use of an at-line automated titrator named TITAAN (TITrimetric Automated ANalyser) is presented. The completely automated sensor enables us to track nitrification rate trend with time in an SBR, detecting the causes leading to slower specific nitrification rates. It was also possible to perform early detection of toxic compounds in the influent by assessing their effect on the nitrifying biomass. Nitrifications rates were determined with average errors+/-10% (on 26 tests), never exceeding 20% as compared with UV-spectrophotometric determinations. PMID:18701782

  10. A real-time data acquisition and processing system for the analytical laboratory automation of a HTR spent fuel reprocessing facility

    International Nuclear Information System (INIS)

    A real-time data acquisition and processing system for the analytical laboratory of an experimental HTR spent fuel reprocessing facility is presented. The on-line open-loop system combines in-line and off-line analytical measurement procedures including data acquisition and evaluation as well as analytical laboratory organisation under the control of a computer-supported laboratory automation system. In-line measurements are performed for density, volume and temperature in process tanks and registration of samples for off-line measurements. Off-line computer-coupled experiments are potentiometric titration, gas chromatography and X-ray fluorescence analysis. Organisational sections like sample registration, magazining, distribution and identification, multiple data assignment and especially calibrations of analytical devices are performed by the data processing system. (orig.)

  11. Integration and global analysis of isothermal titration calorimetry data for studying macromolecular interactions.

    Science.gov (United States)

    Brautigam, Chad A; Zhao, Huaying; Vargas, Carolyn; Keller, Sandro; Schuck, Peter

    2016-05-01

    Isothermal titration calorimetry (ITC) is a powerful and widely used method to measure the energetics of macromolecular interactions by recording a thermogram of differential heating power during a titration. However, traditional ITC analysis is limited by stochastic thermogram noise and by the limited information content of a single titration experiment. Here we present a protocol for bias-free thermogram integration based on automated shape analysis of the injection peaks, followed by combination of isotherms from different calorimetric titration experiments into a global analysis, statistical analysis of binding parameters and graphical presentation of the results. This is performed using the integrated public-domain software packages NITPIC, SEDPHAT and GUSSI. The recently developed low-noise thermogram integration approach and global analysis allow for more precise parameter estimates and more reliable quantification of multisite and multicomponent cooperative and competitive interactions. Titration experiments typically take 1-2.5 h each, and global analysis usually takes 10-20 min. PMID:27055097

  12. Study and Application of a New On—Line Titration Technique

    Institute of Scientific and Technical Information of China (English)

    朱建育; 施利毅; 等

    2002-01-01

    A new on-line titration method and device based on a new technique-continuous flow titration is described.By the means of electronically controlled switching of a solenoid valve,the main component of the system,the equivalent point of the titration is easily determined.Several kinds of mixing tools were examined.whereby a self-made mixing chamer with minimum volume gave best results and was therefore used in the dveice,The error of the titration is within 0.2% and the relative standard deviation(RSD) is below 1.2%,The results show no difference compared with a commercial device,meanwhile the new on-line titration system is cheaper and fully automated and thus easy to hand and less slovent consumption.

  13. Physico-chemical studies on the composition of complex thiosulphates of metals Part VI: Potentiometric studies on the reaction between cadmium nitrate and sodium thiosulphate

    Directory of Open Access Journals (Sweden)

    M. S. Bhadraver

    1962-07-01

    Full Text Available The  formation and composition of cadmium thiosulphate complex has been studied  by potentiometric titrations between cadmium nitrate and sodium thiosulphate both by direct and the inverse methods.the equivalence point obtained from the maximum value of De/Dc corresponds to t e formation of a compound having the composition CdS2O3 when Cd (NO32 was added from a micro-burette to sodium thiosulphate in the electtode vessel.

  14. High-sensitivity titration microcalorimeter

    Science.gov (United States)

    Velikov, A. A.; Grigoryev, S. V.; Chuikin, A. V.

    2015-02-01

    A differential titration microcalorimeter for studying intermolecular interactions in solutions has been designed. To increase the speed of the instrument, the dynamic correction method has been used. It has been shown that electrical calibration of the microcalorimeter is consistent with its chemical calibration. The use of the instrument for measuring the integral heats of dilution of 1-propanol has been demonstrated.

  15. Stuides on a Pb2+-selective electrode with a macrocyclic liquid membrane. Potentiometric determination of Pb2+ ions

    Directory of Open Access Journals (Sweden)

    MARIAN ISVORANU

    2006-12-01

    Full Text Available This paper presents experimental and theoretical data regarding the design, characterization and analytical applications of a non-expensive, liquid-membrane ion-selective electrode for Pb2+ ions. The membrane is a solution of the active complex formed by Pb2+ ions with dibenzo-18-crown-6-ionophore (DB-[18]-C-6 extracted in propylene carbonate (PC. The sucessful application of the developed electrode for the determination of Pb2+ ions in aqueos solution samples by direct potentiometry and potentiometric titration is presented. For the presented analytical results, there are insignificant systematic errors between the direct potentiometric method with the developed ion-selective electrode and atomic absorption spectrometry.

  16. Free Software Development. 3. Numerical Description of Soft Acid with Soft Base Titration

    OpenAIRE

    JÄNTSCHI, Lorentz; Horea Iustin NAŞCU

    2002-01-01

    The analytical methods of qualitative and quantitative determination of ions in solutions are very flexible to automation. The present work is focus on modeling the process of titration and presents a numerical simulation of acid-base titration. A PHP program to compute all iterations in titration process that solves a 3th rank equation to find value of pH for was built and is available through http internet protocol at the address: http://vl.academicdirect.org/molecular_dynamics/ab_titra...

  17. Simple Potentiometric Determination of Reducing Sugars

    Science.gov (United States)

    Moresco, Henry; Sanson, Pedro; Seoane, Gustavo

    2008-01-01

    In this article a potentiometric method for reducing sugar quantification is described. Copper(II) ion reacts with the reducing sugar (glucose, fructose, and others), and the excess is quantified using a copper wire indicator electrode. In order to accelerate the kinetics of the reaction, working conditions such as pH and temperature must be…

  18. Isothermal Titration Calorimetry of RNA

    OpenAIRE

    Salim, Nilshad N.; Feig, Andrew L.

    2008-01-01

    Isothermal titration calorimetry (ITC) is a fast and robust method to study the physical basis of molecular interactions. A single well-designed experiment can provide complete thermodynamic characterization of a binding reaction, including Ka, ΔG, ΔH, ΔS and reaction stoichiometry (n). Repeating the experiment at different temperatures allows determination of the heat capacity change (ΔCP) of the interaction. Modern calorimeters are sensitive enough to probe even weak biological interactions...

  19. Potentiometric determination of free acidity in presence of hydrolysable ions and a sequential determination of hydrazine.

    Science.gov (United States)

    Ganesh, S; Khan, Fahmida; Ahmed, M K; Pandey, S K

    2011-08-15

    A simple potentiometric method for the determination of free acidity in presence of hydrolysable ions and sequential determination of hydrazine is developed and described. Both free acid and hydrazine are estimated from the same aliquot. In this method, free acid is titrated with standard sodium carbonate solution after the metal ions in solutions are masked with EDTA. Once the end point for the free acid is determined at pH 3.0, an aliquot of formaldehyde is added to liberate the acid equivalent to hydrazine which is then titrated with the same standard sodium carbonate solution using an automatic titration system. The described method is simple, accurate and reproducible. This method is especially applicable to all ranges of nitric acid and heavy metal ion concentration relevant to Purex process used for nuclear fuel reprocessing. The overall recovery of nitric acid is 98.9% with 1.2% relative standard deviation. Hydrazine content has also been determined in the same aliquot with a recovery of nitric acid is 99% with 2% relative standard deviation. The major advantage of the method is that generation of corrosive analytical wastes containing oxalate or sulphate is avoided. Valuable metals like uranium and plutonium can easily be recovered from analytical waste before final disposal. PMID:21726724

  20. ANALYSIS OF EFFLUENT FROM CAUSTIC TREATMENT PLANTS: IMPROVEMENT OF ACCURACY IN THE SIMULTANEOUS POTENTIOMETRIC DETERMINATION OF SULFIDE AND MERCAPTIDE IONS Análisis del efluente de una planta de tratamiento cáustico: mejoras de la precisión en la determinación simultánea potenciométrica de los iones de sulfuro y mercaptido

    OpenAIRE

    Marcio Reboucas; Ana Massa; Marcos Vinicio

    2006-01-01

    Potentiometric titration using silver nitrate for determination of sulfide and mercaptide ions, as defined by the UOP Method 209, has been widely used for quality control of Spent Caustic Neutralization Unit in petroleum industries. However, it has been found this procedure does not provide accurate results for samples taken from units based on Wet Air Oxidation (WAO) technology. Therefore, possible sources of error, such as concominant species, between-analytes interference and titration sol...

  1. Direct Potentiometric Method for Human Stress Determination

    OpenAIRE

    Sakač, N.; Karnaš, M.; Grčić, M.

    2015-01-01

    The application of platinum redox electrode for potentiometric determination of salivary amylase activity as a stress biomarker is described. The candidates were divided into two groups, physical activity – medium intensity exercise (ten candidates), and psychical activity – student exam (thirteen candidates). The experimental data were compared with an adapted theoretical model where the sensor and analyte properties were optimized using Solver and the least-squares criterion to fit a theore...

  2. Flow injection potentiometric determination of pipazethate hydrochloride.

    Science.gov (United States)

    Abdel-Ghani, N T; Shoukry, A F; el Nashar, R M

    2001-01-01

    New plastic membrane electrodes for pipazethate hydrochloride based on pipazethatium phosphotungstate, pipazethatium phosphomolybdate and a mixture of the two were prepared. The electrodes were fully characterized in terms of composition, life span, pH and temperature and were then applied to the potentiometric determination of the pipazethate ion in its pure state and pharmaceutical preparations under batch and flow injection conditions. The selectivity of the electrodes towards many inorganic cations, sugars and amino acids was also tested. PMID:11205518

  3. A Porphyrin Based Potentiometric Sensor for Zn2+ Determination

    Directory of Open Access Journals (Sweden)

    H. Lang

    2003-07-01

    Full Text Available PVC based membranes of disodium salt of porphyrin 3,7,12,17-tetramethyl-8, 13-divinyl 2,18-porphine dipropionic acid (I as ionophore with sodium tetra phenyl borate (NaTPB as anion excluder and dibutyl phthalate (DBP, dioctyl phthalate (DOP, dibutyl butyl phosphonate (DBBP, tris(2- ethyl hexylphosphate (TEP, tri-n-butylphosphate (TBP and 1- chloronaphthalene (CN as plasticizing solvent mediators were prepared and constructed for determination of Zn(II. The PVC based membrane of (I with DBBP as plasticizer and having anion excluder, NaTPB in the ratio PVC: I: NaTPB: DBBP (150: 10: 2: 200 gave the best results in terms of working concentration range (1.3×10-5-1.0 ×10-1M with a Nernstian slope (30.0 mV/decade of activity. The useful pH range of the sensor is 3.0 –7.4, beyond which a drift in potential was observed. The response time of the sensor is 10s and the lifetime was about 2 months during which it could be used without any measurable divergence. It had good stability and reproducibility. The membrane worked satisfactorily in non-aqueous medium up to 40% (v/v non-aqueous content. The selectivity coefficient values indicate that the electrode is highly selective for Zn2+ over a number of other cations except Na+ and Cd2+. Although Na+ and Cd2+ are likely to cause some interference, they would not interfere if present at the concentrations < 1 ×10-5 and < 5 ×10-5 M, respectively. The electrode has been used as an indicator electrode to determine the end point in the potentiometric titration of Zn2+ with EDTA.

  4. Development and validation of an alternative titration method for the determination of sulfate ion in indinavir sulfate

    Directory of Open Access Journals (Sweden)

    Breno de Carvalho e Silva

    2005-02-01

    Full Text Available A simple and rapid precipitation titration method was developed and validated to determine sulfate ion content in indinavir sulfate raw material. 0.1 mol L-1 lead nitrate volumetric solution was used as titrant employing potentiometric endpoint determination using a lead-specific electrode. The United States Pharmacopoeia Forum indicates a potentiometric method for sulfate ion quantitation using 0.1 mol L-1 lead perchlorate as titrant. Both methods were validated concerning linearity, precision and accuracy, yielding good results. The sulfate ion content found by the two validated methods was compared by the statistical t-student test, indicating that there was no statistically significant difference between the methods.

  5. Recruitment Maneuvers and PEEP Titration.

    Science.gov (United States)

    Hess, Dean R

    2015-11-01

    The injurious effects of alveolar overdistention are well accepted, and there is little debate regarding the importance of pressure and volume limitation during mechanical ventilation. The role of recruitment maneuvers is more controversial. Alveolar recruitment is desirable if it can be achieved, but the potential for recruitment is variable among patients with ARDS. A stepwise recruitment maneuver, similar to an incremental PEEP titration, is favored over sustained inflation recruitment maneuvers. Many approaches to PEEP titration have been proposed, and the best method to choose the most appropriate level for an individual patient is unclear. A PEEP level should be selected that balances alveolar recruitment against overdistention. The easiest approach to select PEEP might be according to the severity of the disease: 5-10 cm H2O PEEP in mild ARDS, 10-15 cm H2O PEEP in moderate ARDS, and 15-20 cm H2O PEEP in severe ARDS. Recruitment maneuvers and PEEP should be used within the context of lung protection and not just as a means of improving oxygenation. PMID:26493593

  6. Potentiometric Zinc Ion Sensor Based on Honeycomb-Like NiO Nanostructures

    Directory of Open Access Journals (Sweden)

    Magnus Willander

    2012-11-01

    Full Text Available In this study honeycomb-like NiO nanostructures were grown on nickel foam by a simple hydrothermal growth method. The NiO nanostructures were characterized by field emission electron microscopy (FESEM, high resolution transmission electron microscopy (HRTEM and X-ray diffraction (XRD techniques. The characterized NiO nanostructures were uniform, dense and polycrystalline in the crystal phase. In addition to this, the NiO nanostructures were used in the development of a zinc ion sensor electrode by functionalization with the highly selective zinc ion ionophore 12-crown-4. The developed zinc ion sensor electrode has shown a good linear potentiometric response for a wide range of zinc ion concentrations, ranging from 0.001 mM to 100 mM, with sensitivity of 36 mV/decade. The detection limit of the present zinc ion sensor was found to be 0.0005 mM and it also displays a fast response time of less than 10 s. The proposed zinc ion sensor electrode has also shown good reproducibility, repeatability, storage stability and selectivity. The zinc ion sensor based on the functionalized NiO nanostructures was also used as indicator electrode in potentiometric titrations and it has demonstrated an acceptable stoichiometric relationship for the determination of zinc ion in unknown samples. The NiO nanostructures-based zinc ion sensor has potential for analysing zinc ion in various industrial, clinical and other real samples.

  7. Risks and benefits of rapid clozapine titration

    Directory of Open Access Journals (Sweden)

    Jeannie D. Lochhead

    2016-05-01

    Full Text Available Clozapine is often considered the gold standard for the treatment of schizophrenia. Clinical guidelines suggest a gradual titration over 2 weeks to reduce the risks of adverse events such as seizures, hypotension, agranulocytosis, and myocarditis. The slow titration often delays time to therapeutic response. This raises the question of whether, in some patients, it may be safe to use a more rapid clozapine titration. The following case illustrates the potential risks associated with the use of multiple antipsychotics and rapid clozapine titration. We present the case of a young man with schizophrenia who developed life threatening neuroleptic malignant syndrome (NMS during rapid clozapine titration and treatment with multiple antipsychotics. We were unable to find another case in the literature of NMS associated with rapid clozapine titration. This case is meant to urge clinicians to carefully evaluate the risks and benefits of rapid clozapine titration, and to encourage researchers to further evaluate the safety of rapid clozapine titration. Rapid clozapine titration has implications for decreasing health care costs associated with prolonged hospitalizations, and decreasing the emotional suffering associated with uncontrolled symptoms of psychosis. Clozapine is considered the most effective antipsychotic available thus efforts should focus on developing strategies that would allow for safest and most efficient use of clozapine to encourage its utilization for treatment resistance schizophrenia.

  8. Nap-titration : An effective alternative for continuous positive airway pressure titration

    NARCIS (Netherlands)

    Hoekema, A; Stegenga, B; Meinesz, AF; van der Hoeven, JH; Wijkstra, PJ

    2006-01-01

    When treating Obstructive Steep Apnea-Hypopnea Syndrome (OSAHS) several alternatives for standard (manual) continuous positive airway pressure (CPAP) titration are feasible. A practical alternative is titration without polysomnography during an afternoon nap (Nap-titration). The aim of the present s

  9. Potentiometric determination of uranium in organic extracts

    International Nuclear Information System (INIS)

    The potentimetric determination of uranium in organic extracts was studied. A mixture of 30% TBP, (tributylphosphate), in carbon tetrachloride was used, with the NBL (New Brunswick Laboratory) titrimetric procedure. Results include a comparative analysis performed on organic extracts of fissium alloys vs those performed on aqueous samples of the same alloys which had been treated to remove interfering elements. Also comparative analyses were performed on sample solutions from a typical scrap recovery operation common in the uranium processing industry. A limited number of residue type materials, calciner products, and presscakes were subjected to analysis by organic extraction. The uranium extraction was not hindered by 30% TBP/CCl4. To fully demonstrate the capabilities of the extraction technique and its compatibility with the NBL potentiometric uranium determination, a series of uranium standards was subjected to uranium extraction with 30% TBP/CCl4. The uranium was then stripped out of the organic phase with 40 mL of H3PO4, 15 mL of H20, and 1 mL of 1M FeSO4 solution. The uranium was then determined in the aqueous phosphoric phase by the regular NBL potentiometric method, omitting only the addition of another 40 mL of H3PO4. Uranium determinations ranging from approximately 20 to 150 mg of U were successfully made with the same accuracy and precision normally achieved. 8 tables

  10. Theoretical considerations and a simple method for measuring alkalinity and acidity in low-pH waters by gran titration

    Science.gov (United States)

    Barringer, J.L.; Johnsson, P.A.

    1996-01-01

    Titrations for alkalinity and acidity using the technique described by Gran (1952, Determination of the equivalence point in potentiometric titrations, Part II: The Analyst, v. 77, p. 661-671) have been employed in the analysis of low-pH natural waters. This report includes a synopsis of the theory and calculations associated with Gran's technique and presents a simple and inexpensive method for performing alkalinity and acidity determinations. However, potential sources of error introduced by the chemical character of some waters may limit the utility of Gran's technique. Therefore, the cost- and time-efficient method for performing alkalinity and acidity determinations described in this report is useful for exploring the suitability of Gran's technique in studies of water chemistry.

  11. Design and fabrication of a miniaturization micro volume auto titrator coupled with electrochemical end-point detector for the determination of acidity of some fruit juice

    Directory of Open Access Journals (Sweden)

    Prinya Masawat

    2008-06-01

    Full Text Available A miniaturization micro volume auto titrator coupled with electrochemical end-point detector was designed and fabricated for the determination of acidity of some Thai citrus fruit juices collected in the northern area of Thailand. The method was based on on-line potentiometric titration of the acid contents with sodium hydroxide. Conditions such as volume of fruit juice sample, volume and concentration of potassium chloride used as supporting electrolyte and flow rate of titrant were optimized by using univariate optimization. A sample throughput of 83 samples h-1 at 0.28 mL/min was achieved with satisfactory results. The results obtained by the proposed method agreed with those obtained by using the standard classical titration method.

  12. Discussion on Improvement of the Acid Standard Solution Titration Method%酸标准溶液标定方法改进探讨

    Institute of Scientific and Technical Information of China (English)

    谢鹏

    2012-01-01

    Objective: To improve the method for titration of standard acid solution. Methods According to interna- tional standard GB601 -2002, this experiment was used THAM as standard substance and applied the MATLAB Wavelet Toolbox functions to calculate the concentration of standard solution so as to determine the end point of ti- tration. The effectiveness of Potentiometric titration and Manual titration were compared. Results To use THAM as standard substance is feasible and the results dont reject the null hypothesis in the 95% confidence interval in both methods. Conclusion To determine the end point of titration, the Potentiometric titration -wavelet transform method is more accurate, easily manipulated and convenient than Manual titration.%目的:改进酸标准溶液标定方法。方法:在用GB601—2002方法配制时,尝试用三羟甲基氨基甲烷(THAM)作基准物,采用MATLAB小波工具箱函数确定滴定终点(化学计量点)并计算标准溶液浓度。结果:THAM作基准物可行,且电位滴定——小波变换法用于标定终点检测,其所得结果与手工滴定结果经统计分析,有95%的把握认为两种方法所得结果无显著差异。结论:电位滴定——小波变换法确定终点比手工指示剂法准确、简单、方便。

  13. Determination of titratable acidity in white wine

    OpenAIRE

    Rajković Miloš B.; Novaković Ivana D.; Petrović Aleksandar

    2007-01-01

    The amount of titration acid in must is in the largest number of cases with in the range 5.0-8.0 g/dm3. Wines, as a rule, contain less acids than must, and according to Regulations, titratable acidity is in the range of 4.0-8.0 g/dm3 expressed in tartaric acid, because a part of tartaric acid is deposited in the form of salts (tartar or argol) during alcohol fermentation. For wines that contain less than 4 g/dm3 of titratable acids there arises a suspicion about their origin, that is, that du...

  14. The Ca(2+)-EDTA chelation as standard reaction to validate Isothermal Titration Calorimeter measurements (ITC).

    Science.gov (United States)

    Ràfols, Clara; Bosch, Elisabeth; Barbas, Rafael; Prohens, Rafel

    2016-07-01

    A study about the suitability of the chelation reaction of Ca(2+)with ethylenediaminetetraacetic acid (EDTA) as a validation standard for Isothermal Titration Calorimeter measurements has been performed exploring the common experimental variables (buffer, pH, ionic strength and temperature). Results obtained in a variety of experimental conditions have been amended according to the side reactions involved in the main process and to the experimental ionic strength and, finally, validated by contrast with the potentiometric reference values. It is demonstrated that the chelation reaction performed in acetate buffer 0.1M and 25°C shows accurate and precise results and it is robust enough to be adopted as a standard calibration process. PMID:27154686

  15. Determination of uranium in PWR spent fuels by coulometric titration method

    International Nuclear Information System (INIS)

    Controlled-potential coulometric titration method was applied in 0.5M sulphuric acid medium for the determination of uranium content in samples of PWR spent fuel. In this study, we discussed some experimental conditions related to the determination of uranium in PWR spent fuel samples. Accuracy(recovery of uranium) for the coulometric determination of 1∼7mg uranium standard was 99.96∼100.88%. Precision(relative standard deviation, rsd) for the coulometric determination(n=3) of 3∼4mg uranium in PWR spent fuel samples was 0.07∼0.68%. Relative error for the results of the potentiometric and coulometric determination of uranium PWR spent fuel samples was +0.65∼-2.76%

  16. Determination of Formation Constants of Co2+,Ni2+,Cu2+and Zn2+ Complexes with Humic and Fulvic Acids by Potentionmetric Titration Method

    Institute of Scientific and Technical Information of China (English)

    DUJIN-ZHOU; LUCHANG-QING; 等

    1994-01-01

    The formation constants of Co2+,Ni2+,Cu2+ and Zn2+ complexes with humic acid(HA) and fulvic acid(FA) in red soil wrer determined by the potentiometric titration method.The constants as a function of composition of the complexation solutions were obtained by two graphical approaches respetively,The formation constants decreased with increasing concentration of metal in the solution,The results provide unambiguous evidence for the heterogeneity of the function groups of humic substances,the formation constants of FA were much smaller than those of HA,and the formation constants of Cu2+ were much greater than those of Co2+ ,Ni2+ and Zn2+,The potentiometric titration methon for determining formation constants are also discussed in the article.

  17. Gasometric titration for dimethylaluminum chloride analysis.

    Science.gov (United States)

    Wang, Lin; Maligres, Peter; Eckenroad, Kyle; Simmons, Bryon

    2016-06-01

    A gasometric titration method was developed to quantitate active alkylaluminum content in dimethylaluminum chloride solution to perform the stoichiometry calculation for the reaction charge. The procedure was reproducible with good precision, and the results showed good correlation with ICP-MS method. The gasometric titration is a simple, inexpensive alternative to analysis via ICP-MS which provides more selective analysis of methylaluminum species without the need for inertion. PMID:27017569

  18. Nanopore Back Titration Analysis of Dipicolinic Acid

    OpenAIRE

    Han, Yujing; Zhou, Shuo; Wang, Liang; Guan, Xiyun

    2014-01-01

    Here we report a novel label-free nanopore back titration method for the detection of dipicolinic acid, a marker molecule for bacterial spores. By competitive binding of the target analyte and a large ligand probe to metal ions, dipicolinic acid could be sensitively and selectively detected. This nanopore back titration approach should find useful applications in the detection of other species of medical, biological, or environmental importance if their direct detection is difficult to achieve.

  19. Kinetic Titration Series with Biolayer Interferometry

    OpenAIRE

    Frenzel, Daniel; Willbold, Dieter

    2014-01-01

    Biolayer interferometry is a method to analyze protein interactions in real-time. In this study, we illustrate the usefulness to quantitatively analyze high affinity protein ligand interactions employing a kinetic titration series for characterizing the interactions between two pairs of interaction patterns, in particular immunoglobulin G and protein G B1 as well as scFv IC16 and amyloid beta (1–42). Kinetic titration series are commonly used in surface plasmon resonance and involve sequentia...

  20. Plutonium titration by controlled potential coulometry

    International Nuclear Information System (INIS)

    The LAMMAN (Nuclear Materials Metrology Laboratory) is the support laboratory of the CETAMA (Analytical Method Committee), whose two main activities are developing analytic methods, and making and characterizing reference materials. The LAMMAN chose to develop the controlled potential coulometry because it is a very accurate analytical technique which allows the connection between the quantity of element electrolysed to the quantity of electricity measured thanks to the Faraday's law: it does not require the use of a chemical standard. This method was first used for the plutonium titration and was developed in the Materials Analysis and Metrology Laboratory (LAMM), for upgrading its performances and developing it to the titration of other actinides. The equipment and the material used were developed to allow the work in confined atmosphere (in a glove box), with all the restrictions involved. Plutonium standard solutions are used to qualify the method, and in particular to do titrations with an uncertainty better than 0.1 %. The present study allowed making a bibliographic research about controlled potential coulometry applied to the actinides (plutonium, uranium, neptunium, americium and curium). A full procedure was written to set all the steps of plutonium titration, from the preparation of samples to equipments storage. A method validation was done to check the full procedure, and the experimental conditions: working range, uncertainty, performance... Coulometric titration of the plutonium from pure solution (without interfering elements) was developed to the coulometric titration of the plutonium in presence of uranium, which allows to do accurate analyses for the analyses of some parts of the reprocessing of the spent nuclear fuel. The possibility of developing this method to other actinides than plutonium was highlighted thanks to voltammetric studies, like the coulometric titration of uranium with a working carbon electrode in sulphuric medium. (author)

  1. New potentiometric transducer based on a Mn(II) [2-formylquinoline thiosemicarbazone] complex for static and hydrodynamic assessment of azides.

    Science.gov (United States)

    Kamel, Ayman H

    2015-11-01

    A new potentiometric transducer for selective recognition of azide is characterized and developed. The PVC plasticized based sensor incorporates Mn(II) [2-formylquinoline thiosemicarbazone] complex in the presence of tri dodecyl methyl ammonium chloride (TDMAC) as a lipophilic cationic additive. The sensor displayed a near-Nernstian response for azide over 1.0×10(-2)-1.0×10(-5) mol L(-1), with an anionic slope of -55.8±0.6 mV decade(-1) and lower limit of detection 0.34 µg mL(-1). The sensor was pH independent in the range 5.5-9 and presented good selectivity features towards several inorganic anions, and it is easily used in a flow injection system and compared with a tubular detector. The intrinsic characteristics of the detector in a low dispersion manifold were determined and compared with data obtained under a hydrodynamic mode of operation. This simple and inexpensive automation, with a good potentiometric detector, enabled the analysis of ~33 samples h(-1) without requiring pre-treatment procedures. The proposed method is also applied to the analysis of trace levels of azide in primer mixtures. Significantly improved accuracy, precision, response time, stability and selectivity were offered by these simple and cost-effective potentiometric sensor compared with other standard techniques. The method has the requisite accuracy, sensitivity and precision to determine azide ions. PMID:26452931

  2. End-point construction and systematic titration error in linear titration curves-complexation reactions

    NARCIS (Netherlands)

    Coenegracht, P.M.J.; Duisenberg, A.J.M.

    1975-01-01

    The systematic titration error which is introduced by the intersection of tangents to hyperbolic titration curves is discussed. The effects of the apparent (conditional) formation constant, of the concentration of the unknown component and of the ranges used for the end-point construction are consid

  3. Coulometric titration at low temperatures-nonstoichiometric silver selenide

    OpenAIRE

    Beck, Gesa K.; Janek, Jürgen

    2003-01-01

    A modified coulometric titration technique is described for the investigation of nonstoichiometric phases at low temperatures. It allows to obtain titration curves at temperatures where the conventional coulometric titration technique fails because of too small chemical diffusion coefficients of the mobile component. This method for indirect coulometric titration is applied to silver selenide between -100 and 100 °C. The titration curves are analyzed on the basis of a defect chemical model an...

  4. Potentiometric assay for acid and alkaline phosphatase

    International Nuclear Information System (INIS)

    Simple potentiometric kinetic assay for evaluation of acid and alkaline phosphatase activity has been developed. Enzymatically catalyzed hydrolysis of monofluorophosphate, the simplest inorganic compound containing P-F bond, has been investigated as the basis of the assays. Fluoride ions formed in the course of the hydrolysis of this specific substrate have been detected using conventional fluoride ion-selective electrode based on membrane made of lanthanum fluoride. The key analytical parameters necessary for sensitive and selective detection of both enzymes have been assessed. Maximal sensitivity of the assays was observed at monofluorophosphate concentration near 10-3 M. Maximal sensitivity of acid phosphatase assay was found at pH 6.0, but pH of 4.8 is recommended to eliminate effects from alkaline phosphatase. Optimal pH for alkaline phosphatase assay is 9.0. The utility of the developed substrate-sensor system for determination of acid and alkaline phosphatase activity in human serum has been demonstrated

  5. Polyelectrolyte assisted charge titration spectrometry: Applications to latex and oxide nanoparticles.

    Science.gov (United States)

    Mousseau, F; Vitorazi, L; Herrmann, L; Mornet, S; Berret, J-F

    2016-08-01

    The electrostatic charge density of particles is of paramount importance for the control of the dispersion stability. Conventional methods use potentiometric, conductometric or turbidity titration but require large amount of samples. Here we report a simple and cost-effective method called polyelectrolyte assisted charge titration spectrometry or PACTS. The technique takes advantage of the propensity of oppositely charged polymers and particles to assemble upon mixing, leading to aggregation or phase separation. The mixed dispersions exhibit a maximum in light scattering as a function of the volumetric ratio X, and the peak position XMax is linked to the particle charge density according to σ∼D0XMax where D0 is the particle diameter. The PACTS is successfully applied to organic latex, aluminum and silicon oxide particles of positive or negative charge using poly(diallyldimethylammonium chloride) and poly(sodium 4-styrenesulfonate). The protocol is also optimized with respect to important parameters such as pH and concentration, and to the polyelectrolyte molecular weight. The advantages of the PACTS technique are that it requires minute amounts of sample and that it is suitable to a broad variety of charged nano-objects. PMID:27153216

  6. Determination of U and Impurities Elements in The Uranium Tetra Fluoride by Potentiometric and Atomic Absorption Spectrophotometric Methods

    International Nuclear Information System (INIS)

    The determination of u and impurities contents in the Uranium tetra fluoride (UF4)has been carried out by potentiometric titration using modified 'Davies-Gray' and atomic absorption spectrophotometric methods. Dissolution process of the powder sample using saturated Al2(SO4)3 solution introduced to determine UF4 compound content in the UF4 sample. The uranium Content in the obtained filtrate is analyzed by potentiometric. The impurities content is determined by ato-Mic absorption spectrophotometric using ammonium oxalate powder in introducing of the sample preparation. The experiment covered the observation on influence of stirring time of UF4 sample dissolution in respect to separate UF4 from its impurities in determination of uranium content. Also the effects of Ammonium Oxalate added and agitating time were observed deal with the sample preparation for the determination of Impurities content.The analysis result found that UF4 content was 96.15 ± 0.04% the relative station 0.7%. However the best impurities determination was achieved by addition of ammonium oxalate powder and 15 Minutes of agitation time at temperature of 8000C

  7. Potentiometric titration for determining the composition and stability of metal(II) alginates and pectinates in aqueous solutions

    Science.gov (United States)

    Kaisheva, N. Sh.; Kaishev, A. Sh.

    2015-07-01

    The compositions and stabilities of Cu2+, Mn2+, Pb2+, Ca2+, Zn2+, Cd2+, Co2+, and Ni2+ alginates and pectinates are determined in aqueous solutions via titrimetry and potentiometry with calculations performed using Bjerrum's method, the curve intersection technique, and the equilibrium shift method. It is found that the interaction between Cu2+ and polyuronides is a stepwise process and, depending on the ligand concentration and the method of determination, Cu2+ alginate can be characterized by its ML, ML2, and ML3 compositions (where M is the metal ion and L is the structural unit of polyuronide) and stability constants logβ = 2.65, 5.00-5.70, and 7.18-7.80, respectively. The compositions of Cu2+ pectinates are ML and ML2 with logβ = 3.00 and 7.64-7.94, respectively. It is concluded that Pb2+, Ca2+, Mn2+, Zn2+, Cd2+, Co2+, and Ni2+ ions form only alginates and pectinates of ML2 composition with logβ values of 3.45 (Pb2+ alginate), 2.20 (Ca2+ alginate), 1.06 (Mn2+ alginate), 3.51 (Pb2+ pectinate), 2.35 (Ca2+ pectinate), and 1.24 (Mn2+ pectinate). The pectinates are shown to be more stable than the alginates, the most stable compounds being those formed by polyuronides and Cu2+. The least stable are those with Mn2+.

  8. Titratable Acidity and Alkalinity of Red Soil Surfaces

    Institute of Scientific and Technical Information of China (English)

    SHAOZONG-CHEN; HEQUN; 等

    1993-01-01

    The surfaces of red soils have an apparent amphoteric character,carrying titratable acidity and titratable alkalinity simultaneously.The titratable acidity arises from deprotonation of hydroxyl groups of hydrous oxide-type surfaces and dissociation of weak-acid functional groups of soil organic matter,while the titratable alkalinity is derived from release of hydroxyl groups of hydrous oxide-type surfaces.The titratable acidity and titratable alkalinity mainly depended on the composition and content of iron and aluminum oxides in the soils.The results showed that the titratable acidity and titratable alkalinity were in significantly positive correlation not only with the content of amorphous aluminum oxide(Alo) and iron oxide(Feo) extracted with acid ammonium oxalate solution,free iron oxide(Fed) extracted with sodium dithionite-citrate-bicarbonate(DCB) and clays,but also with the zero point of charge (ZPC) of the samples.Organic matter made an important contribution to the titratable acidity.the titratable alkalinity was closely correlated with the amount of fluoride ions adsorbed.The titratable acidity and titratable alkalinity of red soils were influenced by parent materials,being in the order of red soil derived from basalt> that from tuff> that from granite.The titratable acidity and titratable alkalinity ware closely related with origination of the variable charges of red soils,and to a certain extent were responsible for variable negative and positive charges of the soils.

  9. 全新在线滴定技术的研究与应用%Study and Application of a New On-Line Titration Technique

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A new on-line titration method and device based on a new technique-continuous flow titration is described. By the meansofelectronically controlled switching of a solenoid valve, the main component of the system, the equivalent point of the titration is easilydetermined. Several kinds of mixing tools were examined, whereby a self-made mixing chamber with minimum volume gave best re-sults and was therefore used in the device. The error of the titration is within 0.2% and the relative standard deviation (RSD) isbe-low 1.2%. The results show no difference compared with a commercial device, meanwhile the new on-line titration system is cheaperand fully automated and thus easy to hand and less solvent consumption.

  10. Direct potentiometric determination of diastase activity in honey.

    Science.gov (United States)

    Sak-Bosnar, Milan; Sakač, Nikola

    2012-11-15

    A novel method for the determination of diastase activity is reported. The method is based on a direct potentiometric measurement of triiodide ion that is released when a starch-triiodide complex is hydrolysed by honey diastase. The increase of free triiodide ion concentration in a sample is found to be directly proportional to the diastase activity of the sample. A response mechanism of the platinum redox electrode is proposed, allowing a calculation of the diastase activity factor (F). The sensor and analyte parameters, including F, were obtained by least squares fitting of potentiometric data using the optimisation function of the Solver add-in of Microsoft Excel. The values of F obtained by the new direct potentiometric method were compared with those obtained using the standard Phadebas method (DN values), and the two values were found to agree within experimental error. Finally, the diastase activity of nine varieties of honey was determined using the novel method developed here. PMID:22868165

  11. Titration Calculations with Computer Algebra Software

    Science.gov (United States)

    Lachance, Russ; Biaglow, Andrew

    2012-01-01

    This article examines the symbolic algebraic solution of the titration equations for a diprotic acid, as obtained using "Mathematica," "Maple," and "Mathcad." The equilibrium and conservation equations are solved symbolically by the programs to eliminate the approximations that normally would be performed by the student. Of the three programs,…

  12. Isothermal Titration Calorimetry in the Student Laboratory

    Science.gov (United States)

    Wadso, Lars; Li, Yujing; Li, Xi

    2011-01-01

    Isothermal titration calorimetry (ITC) is the measurement of the heat produced by the stepwise addition of one substance to another. It is a common experimental technique, for example, in pharmaceutical science, to measure equilibrium constants and reaction enthalpies. We describe a stirring device and an injection pump that can be used with a…

  13. Fe (III - Galactomannan Solid and Aqueous Complexes: Potentiometric, EPR Spectroscopy and Thermal Data

    Directory of Open Access Journals (Sweden)

    Mercê Ana L. R.

    2001-01-01

    Full Text Available Galactomannans can be employed in food industries to modify the final rheological properties of the products. Since they are not absorbed by the living organisms they can also be used in dietary foods. The equilibria involving the interactions of Fe(III and galactomannans and arabinogalactan of several leguminous plants were characterized by potentiometric titrations and EPR spectroscopy. The log of the equilibrium constants for the formation of ML species, where M is the metal ion and L is the monomeric unit of the biopolymers, were 15.4, 14.1 and 18.5, for the galactomannans of C. fastuosa, L. leucocephala and S. macranthera, respectively. Log K values for protonated species (MHL were 3.1, 3.3, and were not detected for the galactomannan of S. macranthera. The log K values for the formation of ML2 were 14.1, 13.3 and 15.2, respectively. Early formation of insoluble products in the equilibrium with arabinogalactan and Fe(III prevented acquisition of reliable data. The solid complexes assays showed a great dipolar interaction between two Fe(III ions in the inner structure of the biopolymer which increased as the degree of substitution of the galactomannan decreased, and also showed the resulting thermal stability. The complexes impart a new possibility of providing essential metal ions in dietary foods since decomplexation of the complexes can occur at different pH values existing in the human body.

  14. New triiodomercurate-modified carbon paste electrode for the potentiometric determination of mercury

    International Nuclear Information System (INIS)

    A new tetrazolium-triiodomercurate-modified carbon paste electrode has been described for the sensitive and selective determination of mercury. The electrode shows a stable, near-Nernstian response for 1x10-3 to 6x10-6 M [HgI3]- at 25 deg. C over the pH range of 4.0-9.0, with an anionic slope of 55.5±0.4 mV. The lower detection limit is 4x10-6 M with a fast response time of 30-50 s. Selectivity coefficients of a number of interfering anions and iodo complexes of some metal ions have been estimated. The interference from many of the investigated ions is negligible. The determination of 1-200 μg/ml of mercury in aqueous solutions shows an average recovery of 98.5% and a mean relative standard deviation of 1.6% at 50.0 μg/ml. The direct determination of mercury in spiked wastewater, metal amalgams and dental alloy gave results that compare favorably with those obtained by the cold vapor atomic absorption spectrometric method. Potentiometric titration of mercury and phenylmercury acetate with standard potassium iodide has been monitored using the developed triiodomercurate-carbon paste electrode (CPE) as an end point indicator electrode

  15. Aluminum(III) selective potentiometric sensor based on morin in poly(vinyl chloride) matrix.

    Science.gov (United States)

    Gupta, Vinod K; Jain, Ajay K; Maheshwari, Gaurav

    2007-06-15

    Al(3+) selective sensor has been fabricated from poly(vinyl chloride) (PVC) matrix membranes containing neutral carrier morin as ionophore. Best performance was exhibited by the membrane having composition as morin:PVC:sodium tetraphenyl borate:tri-n-butylphosphate in the ratio 5:150:5:150 (w/w, mg). This membrane worked well over a wide activity range of 5.0x10(-7) to 1.0x10(-1)M of Al(3+) with a Nernstian slope of 19.7+/-0.1mV/decade of Al(3+) activity and a limit of detection 3.2x10(-7)M. The response time of the sensor is approximately 5s and membrane could be used over a period of 2 months with good reproducibility. The proposed sensor works well over a pH range (3.5-5.0) and demonstrates good discriminating power over a number of mono-, di- and trivalent cations. The sensor can also be used in partially non-aqueous media having up to 20% (v/v) methanol, ethanol or acetone content with no significant change in the value of slope or working activity range. The sensor has also been used in the potentiometric titration of Al(3+) with EDTA and for its determination in zinc plating mud and red mud. PMID:19071785

  16. Conductimetric and potentiometric detection in conventional and microchip capillary electrophoresis.

    Science.gov (United States)

    Tanyanyiwa, Jatisai; Leuthardt, Sandro; Hauser, Peter C

    2002-11-01

    Potentiometric detection is rarely used in separation methods but is promising for certain classes of analytes which can only with difficulty be quantified by more standard methods. Conductimetric detection of ions is very versatile and has recently received renewed interest spurned by the introduction of the capacitively coupled contactless configuration. Both are useful and complementary alternatives to the established optical detection methods, and to the more widely known electrochemical method of amperometry. The simplicity of the electrochemical methods makes them particularly attractive for microfabricated devices, but relatively little work has to date been carried out with regard to potentiometric and conductimetric detection. PMID:12432526

  17. Titration Calorimetry Standards and the Precision of Isothermal Titration Calorimetry Data

    OpenAIRE

    Daumantas Matulis; Jurgita Matulienė; Vilma Petrikaitė; Lina Baranauskienė

    2009-01-01

    Current Isothermal Titration Calorimetry (ITC) data in the literature have relatively high errors in the measured enthalpies of protein-ligand binding reactions. There is a need for universal validation standards for titration calorimeters. Several inorganic salt co-precipitation and buffer protonation reactions have been suggested as possible enthalpy standards. The performances of several commercial calorimeters, including the VP-ITC, ITC200, and Nano ITC-III, were validated using these sug...

  18. Potentiometric and electrokinetic signatures of iron(II) interactions with (a,y)-Fe2O3

    Energy Technology Data Exchange (ETDEWEB)

    Toczydlowska, Diana; Kedra-Krolik, Karolina; Nejbert, Krzysztof; Preocanin, Tajana; Rosso, Kevin M.; Zarzycki, Piotr P.

    2015-05-29

    The role of surface electrostatics on the reductive dissolution of iron (III) oxides is poorly understood, despite its importance in controlling the amount of mobilized iron. We report the potentiometric titration of the a; y -Fe2O3 oxides exposed to reductants and complexing ligands (Fe(II), ascorbate, oxalate, malonate). We monitored in situ surface and potentials, the ratio of mobilized ferric to ferrous ions, and periodically analyzed nanoparticle crystal structure using X-ray diffraction. We found that addition of Fe2+ ions produces a response consistent with the iron solubilityactivity curve, whereas the presence of ascorbate significantly decreases the amount of mobilized Fe(III) due to reduction to Fe(II). In addition, XRD analysis proved that y-Fe2O3 particles remain structurally unchanged along the titration pathway despite iron cycling between aqueous and solid reservoirs. Our studies, suggest that the surface redoxactivity of iron oxides is primarily governed by the balance between Fe(III) and Fe(II) ions in aqueous phase, which may be easily altered by complexing and reducing agents.

  19. Titration of dengue viruses by immunofluorescence in microtiter plates.

    OpenAIRE

    Schoepp, R.J.; Beaty, B J

    1984-01-01

    A fast, reliable, and inexpensive method was developed for titration of dengue viruses in microtiter plates with an indirect fluorescent-antibody technique. No significant differences were found in median infectious dose endpoints of samples titrated in microtiter plates as compared with titrations in multichambered slides.

  20. Thermographic and potentiometric investigations of the thermal degradation of coals

    Energy Technology Data Exchange (ETDEWEB)

    Mel' nichuk, A.Yu.; Fialkov, B.S.; Zakharov, A.G.; Lemke, E.R.

    1981-01-01

    In the reported experiments, various types of solid fuels have been investigated by thermographic method and by determining electron-ion phenomena. The potentiometric method, in combination with the differential thermal method, can give more complete information on the processes taking place in the thermal degradation of fuels. 8 refs.

  1. A Textile-Based Stretchable Multi-Ion Potentiometric Sensor.

    Science.gov (United States)

    Parrilla, Marc; Cánovas, Rocío; Jeerapan, Itthipon; Andrade, Francisco J; Wang, Joseph

    2016-05-01

    A textile-based wearable multi-ion potentiometric sensor array is described. The printed flexible sensors operate favorably under extreme mechanical strains (that reflect daily activity) while offering attractive real-time noninvasive monitoring of electrolytes such as sodium and potassium. PMID:26959998

  2. Comparison of lentiviral vector titration methods

    OpenAIRE

    Debyser Zeger; Baekelandt Veerle; Willems Sofie; Geraerts Martine; Gijsbers Rik

    2006-01-01

    Abstract Background Lentiviral vectors are efficient vehicles for stable gene transfer in dividing and non-dividing cells. Several improvements in vector design to increase biosafety and transgene expression, have led to the approval of these vectors for use in clinical studies. Methods are required to analyze the quality of lentiviral vector production, the efficiency of gene transfer and the extent of therapeutic gene expression. Results We compared lentiviral vector titration methods that ...

  3. Digital movie-based on automatic titrations.

    Science.gov (United States)

    Lima, Ricardo Alexandre C; Almeida, Luciano F; Lyra, Wellington S; Siqueira, Lucas A; Gaião, Edvaldo N; Paiva Junior, Sérgio S L; Lima, Rafaela L F C

    2016-01-15

    This study proposes the use of digital movies (DMs) in a flow-batch analyzer (FBA) to perform automatic, fast and accurate titrations. The term used for this process is "Digital movie-based on automatic titrations" (DMB-AT). A webcam records the DM during the addition of the titrant to the mixing chamber (MC). While the DM is recorded, it is decompiled into frames ordered sequentially at a constant rate of 26 frames per second (FPS). The first frame is used as a reference to define the region of interest (ROI) of 28×13pixels and the R, G and B values, which are used to calculate the Hue (H) values for each frame. The Pearson's correlation coefficient (r) is calculated between the H values of the initial frame and each subsequent frame. The titration curves are plotted in real time using the r values and the opening time of the titrant valve. The end point is estimated by the second derivative method. A software written in C language manages all analytical steps and data treatment in real time. The feasibility of the method was attested by application in acid/base test samples and edible oils. Results were compared with classical titration and did not present statistically significant differences when the paired t-test at the 95% confidence level was applied. The proposed method is able to process about 117-128 samples per hour for the test and edible oil samples, respectively, and its precision was confirmed by overall relative standard deviation (RSD) values, always less than 1.0%. PMID:26592600

  4. Analysis of Cooperativity by Isothermal Titration Calorimetry

    OpenAIRE

    Alan Brown

    2009-01-01

    Cooperative binding pervades Nature. This review discusses the use of isothermal titration calorimetry (ITC) in the identification and characterisation of cooperativity in biological interactions. ITC has broad scope in the analysis of cooperativity as it determines binding stiochiometries, affinities and thermodynamic parameters, including enthalpy and entropy in a single experiment. Examples from the literature are used to demonstrate the applicability of ITC in the characterisation of coop...

  5. A monosegmented-flow Karl Fischer titrator.

    Science.gov (United States)

    de Aquino, Emerson Vidal; Rohwedder, Jarbas José Rodrigues; Pasquini, Celio

    2007-02-28

    A monosegmented volumetric Karl Fischer titrator is described to mechanize the determination of water content in organic solvents. The system is based on the flow-batch characteristics of the monosegmented analysis concept and employs biamperometry to monitor the progress of the titration. The system shows accuracy and precision that are highly independent of the flow rate, does not require calibration, and is carried out in a closed system capable of minimizing contact of the sample and reagents with ambient moisture. Sample volumes in the range of 40-300muL are employed, depending on the water concentration. An automatic dilution is provided to deal with concentrated samples. The consumption of Karl Fischer reagent depends on the water content of the sample but is not larger than 100muL. The system was evaluated for determination of water in ethanol and methanol in the range 0.02-0.5% (w/w). The average relative precision estimated in that range (9-3%) is comparable to that obtained with a larger volume commercial system and no significant difference was observed between the results obtained for the two systems at the 95% confidence level. A complete titration can be performed in less than 5min employing the proposed system. PMID:19071447

  6. Isothermal titration calorimetry: A thermodynamic interpretation of measurements

    International Nuclear Information System (INIS)

    Highlights: ► Literature review shows that many ITC utilizations are based on empirical rules. ► A proper and rigorous thermodynamic interpretation of heats of titration is proposed. ► Heats of titration are independent of the cell type using infinitesimal titrations. ► Heats of interaction between solutes require only two different titration runs. - Abstract: Isothermal titration calorimeters have been developed and in use since the 1960s and the number of applications based on empirical rules to use them steadily increases. In this paper a rigorous study of the physical interpretation of the titration heat and the thermodynamic framework underlying isothermal titration calorimetry are proposed. For infinitesimal titrations, the titration heat is independent of the cell type employed, and the interpretation of the titration heat depends on the titrant composition and on the experiment type. Moreover, for the study of the interaction between two solutes in solution, only a combination of two experiments is necessary, and the result is interpreted as the partial enthalpy of interaction at infinite dilution of the solute contained in the titrant solution.

  7. Strontium (II-Selective Potentiometric Sensor Based on Ester Derivative of 4-tert-butylcalix(8arene in PVC Matrix

    Directory of Open Access Journals (Sweden)

    Jitendra R. Raisoni

    2004-08-01

    Full Text Available Abstract: Membranes of 4-tert-butylcalix(8arene-octaacetic acid octaethyl ester (I as an electroactive material, sodium tetraphenyl borate (NaTPB as an anion excluder, and tri-n-butyl phosphate (TBP as a solvent mediator in poly(vinyl chloride (PVC matrix have been tried for a strontium-selective sensor. The best performance was exhibited by the membrane having a composition 5:100:150:2 (I: PVC: TBP: NaTPB (w/w. This sensor exhibits a good potentiometric response to Sr2+ over a wide concentration range (3.2 × 10 –5 –1.0 × 10 –1 M with a Nernstian slope (30 mV/ decade. The response time of the sensor is 10 s and it has been used for a period of four months without any drift in potentials. The selectivity coefficient values are in the order of 0.01 for mono-, bi-, and trivalent cations which indicate a good selectivity for Sr2+ over a large number of cations. The useful pH range for the sensor was found to be 3-10 and it works well in mixtures with non-aqueous content up to 25 % (v/v. The sensor has been used as an indicator electrode in the potentiometric titration of Sr2+ against EDTA.

  8. Tandem electrochemical desalination-potentiometric nitrate sensing for seawater analysis.

    Science.gov (United States)

    Cuartero, Maria; Crespo, Gastón A; Bakker, Eric

    2015-08-18

    We report on a methodology for the direct potentiometric determination of nitrate in seawater by in-line coupling to an electrochemical desalination module. A microfluidic custom-fabricated thin layer flat cell allows one to electrochemically reduce the chloride concentration of seawater more than 100-fold, from 600 mM down to ∼2.8 mM. The desalinator operates by the exhaustive electrochemical plating of the halides from the thin layer sample onto a silver element as silver chloride, which is coupled to the transfer of the counter cations across a permselective ion-exchange membrane to an outer solution. As a consequence of suppressing the major interference of an ion-exchanger based membrane, the 80 μL desalinated sample plug is passed to a potentiometric flow cell of 13 μL volume. The potentiometric sensor is composed of an all-solid-state nitrate selective electrode based on lipophilic carbon nanotubes (f-MWCNTs) as an ion-to-electron transducer (slope of -58.9 mV dec(-1), limit of detection of 5 × 10(-7) M, and response time of 5 s in batch mode) and a miniaturized reference electrode. Nitrate is successfully determined in desalinated seawater using ion chromatography as the reference method. It is anticipated that this concept may form an attractive platform for in situ environmental analysis of a variety of ions that normally suffer from interference by the high saline level of seawater. PMID:26201537

  9. Silver ion recognition using potentiometric sensor based on recently synthesized isoquinoline-1,3-dione derivatives

    Directory of Open Access Journals (Sweden)

    AJAR KAMAL

    2012-08-01

    Full Text Available The four derivatives of isoquinoline-1,3-dione based on β-lactum (I-IV, have been explored as neutral ionophores for preparing poly(vinylchloride based polymeric membrane electrodes (PME selective to silver(I ions. The addition of sodium tetraphenylborate (NaTPB and dioctylsebacate (DOS as a plasticizer was found to improve the performance of ion selective electrodes. The best performance was obtained with PME-1 based on ionophore I having composition: ionophore (9.2 mg, PVC (100.1 mg, DOS (201.1 mg and NaTPB (1.5 mg in 5 mL tetrahydrofuran. The electrode response was linear with Nernstian slope of 58.44 mV/decade in the concentration range of 1.0 x 10-1 M to 5.0 x 10-6 M and detection limit of 5.83 x 10-6 M. It performs satisfactorily over wide pH range of 1.0-5.5. The proposed sensor can be used over a period of more than three months without any significant drift in potential and shows good selectivity to silver(I ion over a number of cations especially with no interference of mercury(II ions. Sharp end point was obtained when the sensor was used as an indicator electrode for the potentiometric titration of silver(I ions with chloride ions and therefore this electrode (PME-1 could be used for quantitative determination of silver(I ion in synthetic water, silver foil and dental amalgam samples.

  10. Preparation and Application of Automatic Photometric Titration Analyzer Based on Reflective Photometric Sensor%基于反射式光度传感器的自动光度滴定仪的研制及应用

    Institute of Scientific and Technical Information of China (English)

    何艺; 周小锋; 马建丰

    2012-01-01

    研制了一种以颜色变化为滴定终点的自动光度滴定仪,仪器以光度传感器为核心,包括光度探头、滴定装置、AT89S52单片机、电磁阀、二极管和磁力搅拌器等部件。传感器采用开放设计,对溶液吸光度变化反应迅速。仪器用于红醋酸度的测定,所得结果与电位滴定分析法结果相符。%An automatic photometric titration analyzer with color change as end point of titration was prepared. The analyzer consisted of reflective photometric sensor (as core), photometric probe, titration device, AT89S52 monolithic circuit, electromagnetic valve, diode and magnetic stirrer. The open design of sensor leaded to detect the absorbance of solution without delay in titration. The analyzer was applied in the determination of acidity of red vinegar, and the results obtained were in consistency with those obtained by potentiometric titration.

  11. Contribution to the study of beryllium complexes. IX. Chelation of Be2+ ions by 3-hydroxy butanoic and 2-hydroxy 2-methyl propanoic acids, potentiometric study

    International Nuclear Information System (INIS)

    In the field of work on complexation of beryllium, complex equilibria in aqueous solution between beryllium (II) and 3-hydroxybutanoic acid (HA) and 2-hydroxy-2-methyl propanoic acid (HA) were studied by potentiometric (alkalimetric) titration (at ionic strength = 0.5 M by NaClO4 and a temperature T = 25.0 +- 0.10C to show the influence of hydroxyl group in carboxylic ligands. For the system 3-hydroxy butanoic acid, the results show the presence of two mononuclear species: BeA+ and BeA2 and one hydrolized complex: Be3(OH)3A2, but for 2-hydroxy-2-methylpropanoic acid an additional species is identified, in what the alcoolic function is dissociated: Be(H-1A). The formation constants are reported

  12. Potentiometric studies on stepwise biligand complex formation La(III), Pr(III) or Nd(III)-cyclo hexane-1, 2-diaminotetraacetic acid-hydroxy acid

    International Nuclear Information System (INIS)

    Potentiometric studies of the interaction between 1:1 Ln(III)-CDTA binary chelate (where Ln(III) = La(III), Pr(III) or Nd(III); CDTA = cyclohexane-1,2-diamino-N,N,N',N'-tetracetic acid) with certain hydroxy acids such as glycollic (GA), lactic (LA) and malic (MEA) are described. The nature of the titration curves indicates the stepwise addition of the secondary ligand to the initially formed 1:1, M(III)-CDTA binary complex. Formation constants (Ksub(MAL)) of the resulting biligand chelates have been determined at 30 +- 10 and 35 +- 10C and also thermodynamic functions (viz. ΔG,ΔH and ΔS). The order of stability in terms of metal ions has been found to be La(III) LA > GA. (author)

  13. Application Of A Potentiometric Electronic Tongue For The Determination Of Free SO2 And Other Analytical Parameters In White Wines From New Zealand

    Science.gov (United States)

    Mednova, Olga; Kirsanov, Dmitry; Rudnitskaya, Alisa; Kilmartin, Paul; Legin, Andrey

    2009-05-01

    The present study deals with a potentiometric electronic tongue (ET) multisensor system applied for the simultaneous determination of several chemical parameters for white wines produced in New Zealand. Methods in use for wine quality control are often expensive and require considerable time and skilled operation. The ET approach usually offers a simple and fast measurement protocol and allows automation for on-line analysis under industrial conditions. The ET device developed in this research is capable of quantifying the free and total SO2 content, total acids and some polyphenolic compounds in white wines with acceptable analytical errors.

  14. Fabrication of new carbon paste electrodes based on gold nano-particles self-assembled to mercapto compounds as suitable ionophores for potentiometric determination of copper ions

    Directory of Open Access Journals (Sweden)

    Rasoul Pourtaghavi Talemi

    2013-12-01

    Full Text Available In the present study, we investigate the potentiometric behavior of Cu2+ carbon paste electrodes based on two mercapto compounds 2-ethylmino-5-mercapto-1,3,4-thiadiazole (EAMT and 2-acetylamino-5-mercapto-1,3,4-thiadiazole (AAMT self-assembled on gold nano-paricle (GNP as ionophore. Then, the obtained results from the modified electrodes are compared. The self-assembled ionophores exhibit a high selectivity for copper ion (Cu2+, in which the sulfur and nitrogen atoms in their structure play a significant role as the effective coordination donor site for the copper ion. Among these electrodes, the best performance was obtained with the sensor with a EAMT/graphite powder/paraffin oil weight ratio of 4.0/68/28 with 200 µL of GNP which exhibits the working concentration range of 1.6×10−9 to 6.3×10−2 M and a nernstian slope of 28.9±0.4 mVdecade−1 of copper(II activity. The detection limit of electrode was 2.9(±0.2×10−10M and potential response was pH ; in other words, it was independent across the range of 2.8–6.3. The proposed electrode presented very good selectivity and sensitivity towards the Cu2+ ions over a wide variety of cations including alkali, alkaline earth, transition and heavy metal ions. Moreover, the proposed electrode was successfully applied as an indicator electrode in the potentiometric titration of Cu(II ions with EDTA and also the potentiometric determination of copper ions in spiked water samples.

  15. Potentiometric studies on ternary complexes involving some divalent transition metal ions, gallic acid and biologically abundant aliphatic dicarboxylic acids in aqueous solutions

    Directory of Open Access Journals (Sweden)

    Abdelatty Mohamed Radalla

    2015-06-01

    Full Text Available Formation of binary and ternary complexes of the divalent transition metal ions, Cu2+, Ni2+, Co2+ and Zn2+ with gallic acid and the biologically important aliphatic dicarboxylic acids (adipic, succinic, malic, malonic, maleic, tartaric and oxalic acids were investigated by means of the potentiometric technique at 25 °C and I = 0.10 mol dm−3 NaNO3. The acid-base properties of the ligands were investigated and discussed. The acidity constants of gallic acid and aliphatic dicarboxylic acids were determined and used for determining the stability constants of the binary and ternary complexes formed in the aqueous medium under the above experimental conditions. The formation of the different 1:1 and 1:2 binary complexes and 1:1:1 ternary complexes are inferred from the corresponding potentiometric pH-metric titration curves. The ternary complex formation was found to occur in a stepwise manner. The stability constants of these binary and ternary systems were calculated. The values of Δ log K, percentage of relative stabilization (%R.S. and log X were evaluated and discussed. The concentration distribution of the various complex species formed in solution was evaluated and discussed. The mode of chelation of ternary complexes formed was ascertained by conductivity measurements.

  16. A Novel Potentiometric Sensor Based on 1,2-Bis(N’-benzoylthioureido)benzene and Reduced Graphene Oxide for Determination of Lead (II) Cation in Raw Milk

    International Nuclear Information System (INIS)

    We have developed a highly sensitive and selective potentiometric PVC-membrane sensor for lead (II) cation. A glassy carbon electrode (GCE) was modified with synthesized 1,2-Bis(N’-benzoylthioureido) benzene (BBTB) as an ionophore and reduced graphene oxide (RGO), and this material was characterized by scanning electron microscopy. The sensor shows sensitive and highly selective response to Pb(II) ion with a linear range from 6.31 × 10−8 to 3.98 × 10−2 M, Nernstian slope of 30.37 ± 0.62 mV per decade and a detection limit of 2.51 × 10−8 M. The proposed sensor could be used in a pH range of 4.0–8.0. Selectivity coefficients were determined for known common cations by applying the match potential method (MPM). The sensor was successfully applied to monitor Pb(II) in raw milk and in potentiometric titration of Pb2+ ions. The structure of BBTB ligand and its complexation with some common cations were investigated by using quantum mechanical DFT calculations. Lead (II) cation showed prominent affinity to the BBTB carrier

  17. Coulometric titration studies of nonstoichiometric nanocrystalline ceria

    International Nuclear Information System (INIS)

    Oxygen nonstoichiometry measurements in nanocrystalline ceria, x in CeO2-x, were performed using coulometric titration. The measurements reveal large apparent deviations from stoichiometry, of the order of 10-3--10-4 at T = 405--455 C and PO2 = 0.21--10-5 atm, as compared to levels of ∼ 10-9 for coarsened materials under the same conditions. The level of nonstoichiometry is, however, larger then expected from previous electrical conductivity data of nanocrystalline ceria. In addition, x ∝ PO2-1/2 while σ ∝ PO2-1/6. The observed dependence of X(PO2, T) can be explained by either the formation of neutral oxygen vacancies at or near the interface, or by surface adsorption

  18. The coulometric titration of acids and bases in dimethylsulfoxide media

    NARCIS (Netherlands)

    Bos, M.; IJpma, S.T.; Dahmen, E.A.M.F.

    1976-01-01

    The coulometric titration of 20–200 μeq of acids and bases in DMSO media is described. In the titration of bases, the electro-oxidation of hydrogen at a platinized platinum electrode is used as the source of protons. The conditions for 100 % current efficiency at this electrode are low current densi

  19. Microscale pH Titrations Using an Automatic Pipet.

    Science.gov (United States)

    Flint, Edward B.; Kortz, Carrie L.; Taylor, Max A.

    2002-01-01

    Presents a microscale pH titration technique that utilizes an automatic pipet. A small aliquot (1-5 mL) of the analyte solution is titrated with repeated additions of titrant, and the pH is determined after each delivery. The equivalence point is determined graphically by either the second derivative method or a Gran plot. The pipet can be…

  20. New applications of corrosion measurements by titration (CMT)

    DEFF Research Database (Denmark)

    Bech-Nielsen, Gregers

    1998-01-01

    is shown that when aluminium dissolves in alkali, CMT measurements can also be applied, but in this case requiring titration with alkali. Titration with alkali is also required in a special situation, where corrosion of nickel in an acid solution and subsequent formation of a nickel complex results...

  1. Quantitative Analysis of Sulfate in Water by Indirect EDTA Titration

    Science.gov (United States)

    Belle-Oudry, Deirdre

    2008-01-01

    The determination of sulfate concentration in water by indirect EDTA titration is an instructive experiment that is easily implemented in an analytical chemistry laboratory course. A water sample is treated with excess barium chloride to precipitate sulfate ions as BaSO[subscript 4](s). The unprecipitated barium ions are then titrated with EDTA.…

  2. Use of Sequential Injection Analysis to construct a Potentiometric Electronic Tongue: Application to the Multidetermination of Heavy Metals

    Science.gov (United States)

    Mimendia, Aitor; Legin, Andrey; Merkoçi, Arben; del Valle, Manel

    2009-05-01

    An automated potentiometric electronic tongue (ET) was developed for the quantitative determination of heavy metal mixtures. The Sequential Injection Analysis (SIA) technique was used in order to automate the obtaining of input data, and the combined response was modeled by means of Artificial Neural Networks (ANN). The sensor array was formed by four sensors: two based on chalcogenide glasses Cd sensor and Cu sensor, and the rest on poly(vinyl chloride) membranes Pb sensor and Zn sensor. The Ion Selective Electrode (ISE) sensors were first characterized with respect to one and two analytes, by means of high-dimensionality calibrations, thanks to the use of the automated flow system; this characterization enabled an interference study of great practical utility. To take profit of the dynamic nature of the sensor's response, the kinetic profile of each sensor was compacted by Fast Fourier Transform (FFT) and the extracted coefficients were used as inputs for the ANN in the multidetermination applications. In order to identify the ANN which provided the best model of the electrode responses, some of the network parameters were optimized. Finally analyses were performed employing synthetic samples and water samples of the river Ebro; obtained results were compared with reference methods.

  3. Use of Sequential Injection Analysis to construct a Potentiometric Electronic Tongue: Application to the Multidetermination of Heavy Metals

    International Nuclear Information System (INIS)

    An automated potentiometric electronic tongue (ET) was developed for the quantitative determination of heavy metal mixtures. The Sequential Injection Analysis (SIA) technique was used in order to automate the obtaining of input data, and the combined response was modeled by means of Artificial Neural Networks (ANN). The sensor array was formed by four sensors: two based on chalcogenide glasses Cd sensor and Cu sensor, and the rest on poly(vinyl chloride) membranes Pb sensor and Zn sensor. The Ion Selective Electrode (ISE) sensors were first characterized with respect to one and two analytes, by means of high-dimensionality calibrations, thanks to the use of the automated flow system; this characterization enabled an interference study of great practical utility. To take profit of the dynamic nature of the sensor's response, the kinetic profile of each sensor was compacted by Fast Fourier Transform (FFT) and the extracted coefficients were used as inputs for the ANN in the multidetermination applications. In order to identify the ANN which provided the best model of the electrode responses, some of the network parameters were optimized. Finally analyses were performed employing synthetic samples and water samples of the river Ebro; obtained results were compared with reference methods.

  4. Neurochip Based on Light-addressable Potentiometric Sensor

    Institute of Scientific and Technical Information of China (English)

    Qingjun Liu; Hua Cai; Ying Xu; Lifeng Qin; Lijiang Wang; Ping Wang

    2006-01-01

    A novel neurochip based on light addressable potentiometric sensor (LAPS) is designed. Using its light addressable characteristic. The problems of the limitations of restricted discrete active sites of current neurochips, such as microelectrode array and field effect transistor array can be settled easily. Based on the theoretical analysis of the interface between cells and LAPS, spontaneously discharges of hippocampal neurons induced by Mg2+-free media treatment were recorded by LAPS. The results demonstrate that this kind of neurochip has potential to monitor electrophysiology of cultured cells in a non-invasive way.

  5. Limitations of potentiometric oxygen sensors operating at low oxygen levels

    DEFF Research Database (Denmark)

    Lund, Anders; Jacobsen, Torben; Hansen, Karin Vels;

    2011-01-01

    The electrochemical processes that limit the range of oxygen partial pressures in which potentiometric oxygen sensors can be used, were analysed using a theoretical and an experimental approach. Electrochemical impedance spectroscopy was performed on porous Pt/yttria stabilised zirconia (YSZ......) electrodes between 10−6 and 0.2 bar and at temperatures between 500 and 950 °C. The flow of oxide ions and electron holes through a sensor cell, with a YSZ electrolyte, were calculated under similar conditions. The oxygen permeation of the sensor cell was insignificant at an oxygen partial pressure of 10...... oxygen sensors can be used....

  6. New conventional coated-wire ion-selective electrodes for flow-injection potentiometric determination of chlordiazepoxide.

    Science.gov (United States)

    Issa, Y M; Abdel-Ghani, N T; Shoukry, A F; Ahmed, Howayda M

    2005-09-01

    New chlordiazepoxide hydrochloride (Ch-Cl) ion-selective electrodes (conventional type) based on ion associates, chlordiazepoxidium-phosphomolybdate (I) and chlordiazepoxidium-phosphotungstate (II), were prepared. The electrodes exhibited mean slopes of calibration graphs of 59.4 mV and 60.8 mV per decade of (Ch-Cl) concentration at 25 degrees C for electrodes (I) and (II), respectively. Both electrodes could be used within the concentration range 3.16 x 10(-6)-1 x 10(-2) M (Ch-Cl) within the pH range 2.0-4.5. The standard electrode potentials were determined at different temperatures and used to calculate the isothermal coefficients of the electrodes, which were 0.00139 and 0.00093 V degrees C(-1) for electrodes (I) and (II), respectively. The electrodes showed a very good selectivity for Ch-Cl with respect to the number of inorganic cations, amino acids and sugars. The electrodes were applied to the potentiometric determination of the chlordiazepoxide ion and its pharmaceutical preparation under batch and flow injection conditions. Also, chlordiazepoxide was determined by conductimetric titrations. Graphite, copper and silver coated wires were prepared and characterized as sensors for the drug under investigation. PMID:16363470

  7. N′, N″, N‴-tris(2-pyridyloxymethyl) ethane as ionophore in potentiometric sensor for Pb(II) ions

    Indian Academy of Sciences (India)

    Pawan Kumar; Ashok Kumar S K; Susheel K Mittal

    2014-01-01

    N′,N″,N‴ tris(2-pyridyloxymethyl) ethane (TPOME) has been used as an ionophore in a polyvinylchloride (PVC)-based membrane. Membrane electrode with a composition 30:5:62:3 (PVC:TPOME: o-NPOE:NaTPB) exhibits Nernstian response towards Pb(II) ions with a slope of 30mV/decade, over a concentration range of 1 × 10−5 M to 1 × 10−1 M. Potential response remains almost unchanged over pH range of 3.7-6.4. The electrode shows fast response time of 15 ± 2 s and a lifetime of four months. It shows good selectivity for Pb(II) ions over other mono-, di- and trivalent cations. Electrode response is satisfactory in mixed solvent media up to 30% (v/v) non-aqueous contents. Selectivity of the ionophore for Pb(II) ions was determined by spectrophotometric method. The electrode can also be used as an indicator electrode in potentiometric titration of Pb(II) ions with standard chromate solution and its determination in real-life samples. Surface morphology of membrane electrode at different stages of its development and use is also discussed.

  8. Determination of complexable metals by chelometric titration

    International Nuclear Information System (INIS)

    A rapid, simple method for the determination of total complexable metal ions (Fe3+, Al3+, Mn2+, Ni2+, Co2+, Pb2+, and Rare Earths) in feed to the Hanford strontium recovery process has been developed. The method consists of complexing the metal ions with EDTA and titrating the excess with copper (II) ion. Pyrocatechol violet is used as a colorimetric end point indicator. Samples of actual process feed were analyzed and the results compared very favorably with results by atomic absorption. Use of a synthetic feed standard showed an average accuracy of 99.7% and a relative precision of +- 1.9% (95% C.L.). Interference studies run on the method show that oxalate and phosphate interfere above mole ratios of 0.1 and 0.3, respectively (anion : total complexable cations). Of the complexable metal ions commonly encountered in this feed (specifically excluding alkali and alkaline-earth metals), the only complexable ion not determinable by this method is Cr

  9. Titration and hysteresis in epigenetic chromatin silencing

    International Nuclear Information System (INIS)

    Epigenetic mechanisms of silencing via heritable chromatin modifications play a major role in gene regulation and cell fate specification. We consider a model of epigenetic chromatin silencing in budding yeast and study the bifurcation diagram and characterize the bistable and the monostable regimes. The main focus of this paper is to examine how the perturbations altering the activity of histone modifying enzymes affect the epigenetic states. We analyze the implications of having the total number of silencing proteins, given by the sum of proteins bound to the nucleosomes and the ones available in the ambient, to be constant. This constraint couples different regions of chromatin through the shared reservoir of ambient silencing proteins. We show that the response of the system to perturbations depends dramatically on the titration effect caused by the above constraint. In particular, for a certain range of overall abundance of silencing proteins, the hysteresis loop changes qualitatively with certain jump replaced by continuous merger of different states. In addition, we find a nonmonotonic dependence of gene expression on the rate of histone deacetylation activity of Sir2. We discuss how these qualitative predictions of our model could be compared with experimental studies of the yeast system under anti-silencing drugs. (paper)

  10. Improving the limits of detection in potentiometric sensors

    International Nuclear Information System (INIS)

    Potentiometric sensors will generally suffer from unwanted responses as a result to changing temperatures by generating an electromotive force. Typically, this voltage drift has a non-linear character and therefore it is difficult to compensate using linear algorithms implemented in the analogue domain. A solution is proposed to improve the sensor characteristics by combining the digitized output of two CO2 rubidium silver iodide sensors with a specially designed digital algorithm to improve the limits of detection (LOD). Experiments show that this method has the capability to improve the LOD of the sensor with a factor 4.5x during temperature variations of 22 °C over a measurement period of 22 h. It enables potentiometric sensors to be used in low power wireless sensor networks for long term air quality control. Furthermore, the influence of depletion of the rubidium silver iodide electrolyte layer can be effectively compensated by determining the decay of the active layer according to the Nernst equation. Knowing the function of depletion over time helps to correct the sensor output and thereby improves the accuracy of the sensor. (paper)

  11. Improving the limits of detection in potentiometric sensors

    Science.gov (United States)

    van der Bent, J. F.; Puik, E. C. N.; Tong, H. D.; van Rijn, C. J. M.

    2015-12-01

    Potentiometric sensors will generally suffer from unwanted responses as a result to changing temperatures by generating an electromotive force. Typically, this voltage drift has a non-linear character and therefore it is difficult to compensate using linear algorithms implemented in the analogue domain. A solution is proposed to improve the sensor characteristics by combining the digitized output of two CO2 rubidium silver iodide sensors with a specially designed digital algorithm to improve the limits of detection (LOD). Experiments show that this method has the capability to improve the LOD of the sensor with a factor 4.5x during temperature variations of 22 °C over a measurement period of 22 h. It enables potentiometric sensors to be used in low power wireless sensor networks for long term air quality control. Furthermore, the influence of depletion of the rubidium silver iodide electrolyte layer can be effectively compensated by determining the decay of the active layer according to the Nernst equation. Knowing the function of depletion over time helps to correct the sensor output and thereby improves the accuracy of the sensor.

  12. Highly sensitive potentiometric immunosensor for hepatitis B surface antigen diagnosis

    Institute of Scientific and Technical Information of China (English)

    YUAN Ruo; TANG Dianping; CHAI Yaqin; ZHANG Lingyan; LIU Yan; ZHONG Xia; DAI Jianyuan

    2005-01-01

    A highly sensitive potentiometric immunosensor for the diagnoses of epidemic diseases has been developed by means of self-assembly to immobilize hepatitis B surface antibody (HBsAb) for the detection of hepatitis B surface antigen (HBsAg) as a model. At first, the Nafion containing -SO3- groups was immobilized on a platinum electrode surface to absorb the -NH3+ groups of antibody molecules via the opposite-charged adsorption technique, in the meantime, hepatitis B surface antibodies were adsorbed onto the surface of Au nanoparticles, then hepatitis B surface antibodies and Au nanopartilces were entrapped into polyvinyl butyral on the surface of Nafion film. The modified procedure was further characterized by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The influence and factors influencing the performance of resulting immunosensor were studied in detail. The resulting immunosensor exhibited sigmoid curve with log HBsAg concentrations, high sensitivity, wide linear range from 26 to 1280 ng·mL-1 with a detection limit of 3.1 ng·mL-1, rapid potentiometric response (4 months). Analytical results of clinical samples show that the developed immunoassay is comparable with the enzyme-linked immunosorbent assays (ELISAs) method, implying a promising alternative approach for detecting HBsAg in the clinical diagnosis.

  13. Rapid Clozapine Titration in Patients with Treatment Refractory Schizophrenia.

    Science.gov (United States)

    Poyraz, Cana Aksoy; Özdemir, Armağan; Sağlam, Nazife Gamze Usta; Turan, Şenol; Poyraz, Burç Çağrı; Tomruk, Nesrin; Duran, Alaattin

    2016-06-01

    The aim of this study is to evaluate the safety and effectiveness of rapid clozapine titration in patients with schizophrenia in hospital settings. We conducted a retrospective two-center cohort study to compare the safety and effectiveness of clozapine with different titration rates in treatment-refractory patients with schizophrenia. In the first center, clozapine was started at 25-50 mg followed by 50-100 mg as needed every 6 h on day 1, followed by increases of 50-100 mg/day. In the second center, titration was slower; clozapine initiated with 12.5-50 mg on day 1 followed by increases of 25-50 mg/day. The number of days between starting of clozapine until discharge was shorter in the rapid titration group (22.4 ± 8.72 vs 27.0 ± 10.5, p = 0.1). Number of days of total hospital stay were significantly shorter in the rapid titration group (29.6 ± 10.6 vs 41.2 ± 14.8, p = 0.002). Hypotension was more common in the rapid titration group and one patient had suspected myocarditis. Rapid clozapine titration appeared safe and effective. The length of stay following initiation of clozapine was shorter in the rapid-titration group, although this was not statistically significant. However starting clozapine earlier together with rapid titration has significantly shortened the length of hospital stay in patients with treatment refractory schizophrenia. PMID:26433727

  14. Novel titration method for surface-functionalised silica

    International Nuclear Information System (INIS)

    This paper describes three inexpensive and fast analytical methods to characterise grafted particle surfaces. The reaction of silica with (3-aminopropyl)triethoxysilane, (3-mercaptopropyl)trimethoxysilane and N-(phosphonomethyl)iminodiacetic acid hydrate, respectively, leads to NH2-, SO3H- or COOH-functionalised silica, which were characterised by X-ray photoelectron spectrometry and titration in nonaqueous media as well as with two titration methods in a water-based environment. In the work presented, factors influencing the titrations are pointed out and solutions are presented to overcome these limiting factors are shown.

  15. Automatic photometric titrations of calcium and magnesium in carbonate rocks

    Science.gov (United States)

    Shapiro, L.; Brannock, W.W.

    1955-01-01

    Rapid nonsubjective methods have been developed for the determination of calcium and magnesium in carbonate rocks. From a single solution of the sample, calcium is titrated directly, and magnesium is titrated after a rapid removal of R2O3 and precipitation of calcium as the tungstate. A concentrated and a dilute solution of disodium ethylenediamine tetraacetate are used as titrants. The concentrated solution is added almost to the end point, then the weak solution is added in an automatic titrator to determine the end point precisely.

  16. The hydrolysis and precipitation of Pd(II) in 0.6 mol kg-1 NaCl: A potentiometric, spectrophotometric, and EXAFS study

    International Nuclear Information System (INIS)

    The hydrolysis of palladium was investigated in 0.6 mol kg-1 NaCl at 298.2 K. Potentiometric titrations of solutions at various total concentrations of palladium(II) revealed that dilute (millimolar) conditions can be used to monitor the proton release due to hydrolysis reactions up to 2 protons per palladium(II) as long as the equilibration time is kept small. Spectrophotometric titrations were used to corroborate the homogeneous changes in speciation for the PdCl3OH2- species and to extract its correlative molar absorption coefficients in the 210-320 nm range. The molar absorption coefficients are similar to those of PdCl42- but exhibit a broader distribution of excitation energies resulting from the blue shift of the dominant charge transfer bands due to the presence of OH-. The longer-term potentiometric titrations systematically yielded, on the other hand, precipitates which matured over a period of 6 weeks and resulted in a more extensive release of protons to the solution. Precipitation experiments at six different total palladium(II) concentrations in the 3-11 pH range showed the dominant precipitating phase as Pd(OH)1.72Cl0.28. The coordination environment of Pd in this solid was investigated by extended X-ray absorption fine structure spectroscopy (EXAFS) and yielded an average 1.75 O and 0.25 Cl per Pd atoms with a Pd-O distance of 2.0 (angstrom) and Pd-Cl of 2.1 (angstrom). Finally, the precipitation experiments showed the final products to be of larger solubility than a literature Pd(OH)2 solubility study in which the KCl media induced a solid phase transformation to Pd(OH)1.72Cl0.28. Polynuclear complexes Pdq(OH)r2q-r with q=r=[3,9] explain the combined precipitation and hydrolysis data and may represent subsets of [Pd(OH)2]n and/or [Pd(OH)1.72Cl0.28]n chains coiled into nanometer-sized spheroids previously described in the literature

  17. Home Automation

    OpenAIRE

    Ahmed, Zeeshan

    2010-01-01

    In this paper I briefly discuss the importance of home automation system. Going in to the details I briefly present a real time designed and implemented software and hardware oriented house automation research project, capable of automating house's electricity and providing a security system to detect the presence of unexpected behavior.

  18. Potentiometric-level monitoring program: Mississippi and Louisiana. Annual status report for fiscal year 1984

    International Nuclear Information System (INIS)

    Potentiometric-level data presented in this report were collected from October 1983 through September 1984 at 79 wells in Mississippi and Louisiana. These wells are located near Richton and Cypress Creek Domes in Mississippi and Vacherie Dome in Louisiana. Fourteen wells were added to the program during this period. Two of these wells were not measurable. Two wells previously unmeasurable were located and measured. One well was destroyed during military maneuvers in the area. Analysis of the data indicated minimal, if any, change in potentiometric levels during the past year in the Citronelle, Hattiesburg, Cockfield, Sparta, and Wilcox Formations in Mississippi. A continuing decline in potentiometric levels, ranging from 0.3 to 0.6 foot per year, occurred in the wells screened in the caprock at Richton and Cypress Creek Domes. The Catahoula Formation experienced a continuing decline in potentiometric levels of about 2 feet per year. Two wells in the Cook Mountain Formation showed a continuing rise in potentiometric levels ranging from 8 to 30 ft during the past fiscal year. Wells screened in the Austin Formation in Louisiana showed a fall in potentiometric levels of 2 to 3 ft over the past fiscal year. Other formations in Louisiana generally showed no change in potentiometric levels over the past year. 26 refs., 2 figs., 3 tabs

  19. Microscope Titration and Extraction of DNA from Liver.

    Science.gov (United States)

    Mayo, Lois T.; And Others

    1993-01-01

    Describes a simple and inexpensive, one-period activity to extract DNA to make the study of DNA less abstract. A microscope titration is used to determine when cells are ready for DNA extraction. (PR)

  20. A microcomputer-controlled system for titration analysis

    OpenAIRE

    Boelema, Gerrit Jan

    1982-01-01

    This thesis deals with the results of the implementation of microprocessor technology in automatic titration equipment to obtain a versatile system for pharmaceutical, chemical analytical and optimization research purposes. ... Zie: Summary

  1. Analysis of the Purity of Cetrimide by Titrations

    DEFF Research Database (Denmark)

    Andersen, Jens Enevold Thaulov; Rasmussen, Claus/Dallerup; Nielsen, Hans/Boye

    2006-01-01

    The purity of cetrimide, trimethyl tetradecyl ammonium bromide (TTAB), that is an important preservative of many cosmetic and pharmaceutical products, was determined by three independent methods of titration. Traditionally, cetrimide was analysed by an assay method of the European Pharmacopoeia (Ph....... Eur.), which showed consistently a low purity of cetrimide with large standard deviations associated, however. A systematic 3% bias of the Ph. Eur. assay method was identified by comparing the result with results of two alternative methods of titration that exhibited high precision and high accuracy....... Titration by perchloric acid showed a 99.69 ± 0.05 % purity of cetrimide and titration by silver nitrate showed a 99.85% ± 0.05 % purity while the traditional assay method predicted a purity of only 97.1 ± 0.4. It was found that the discrepancy could be identified as differences in selectivity during the...

  2. Analysis of the Purity of Cetrimide by Titrations

    DEFF Research Database (Denmark)

    Andersen, Jens Enevold Thaulov; Rasmussen, Claus/Dallerup; Nielsen, Hans/Boye

    2006-01-01

    The purity of cetrimide, trimethyl tetradecyl ammonium bromide (TTAB), that is an important preservative of many cosmetic and pharmaceutical products, was determined by three independent methods of titration. Traditionally, cetrimide was analysed by an assay method of the European Pharmacopoeia (...

  3. A Titration Technique for Demonstrating a Magma Replenishment Model.

    Science.gov (United States)

    Hodder, A. P. W.

    1983-01-01

    Conductiometric titrations can be used to simulate subduction-setting volcanism. Suggestions are made as to the use of this technique in teaching volcanic mechanisms and geochemical indications of tectonic settings. (JN)

  4. Infrared Turbidimetric Titration Method for Sulfate Ions in Brackish Water

    OpenAIRE

    Benabadji Nouredine; Kherici Samira; Benouali Djillali

    2012-01-01

    In this work an infrared turbidimetric titration method is described for the determination of sulfate ions in brackish water. A suspension of barium sulfate is produced in an aqueous solution and/or brackish water sample by the addition of barium chloride solution and the turbidity is monitored with the help of an immersed infrared sensor. The developed sensor utilizes an optical system to measure the evolution of turbidity during the titration. This sensor is a simple device designed in th...

  5. Reliability of home CPAP titration with different automatic CPAP devices

    OpenAIRE

    Lacasse Yves; Plante Julie; Sériès Frédéric

    2008-01-01

    Abstract Background CPAP titration may be completed by automatic apparatus. However, differences in pressure behaviour could interfere with the reliability of pressure recommendations. Our objective was to compare pressure behaviour and effective pressure recommendations between three Automatic CPAP machines (Autoset Spirit, Remstar Auto, GK 420). Methods Sixteen untreated obstructive sleep apnea patients were randomly allocated to one of the 3 tested machines for a one-week home titration tr...

  6. Carbon Nanotubes-Based Potentiometric Bio-Sensors for Determination of Urea

    Directory of Open Access Journals (Sweden)

    Ewa Jaworska

    2015-07-01

    Full Text Available The possibility of using disposable plastic-carbon potentiometric sensors as enzyme biosensors was examined. Urease enzyme was immobilized on poly(vinyl chloride based H+- or NH4+-selective membranes using cellulose acetate. This approach has resulted in a potentiometric response on changing the pH of the solution or NH4+ ion content due to an enzymatic reaction that occurs between urease and urea. Both types of potentiometric biosensors for urea were characterized by good analytical parameters as high sensitivity and fast response time.

  7. Modeling potentiometric measurements in topological insulators including parallel channels

    Science.gov (United States)

    Hong, Seokmin; Diep, Vinh; Datta, Supriyo; Chen, Yong P.

    2012-08-01

    The discovery of spin-polarized states at the surface of three-dimensional topological insulators (TI) like Bi2Te3 and Bi2Se3 motivates intense interests in possible electrical measurements demonstrating unique signatures of these unusual states. Here we show that a three-terminal potentiometric set-up can be used to probe them by measuring the voltage change of a detecting magnet upon reversing its magnetization. We present numerical results using a nonequilibrium Green's function (NEGF)-based model to show the corresponding signal quantitatively in various transport regimes. We then provide an analytical expression for the resistance (the measured voltage difference divided by an applied current) that agrees with NEGF results well in both ballistic and diffusive limits. This expression is applicable to TI surface states, two-dimensional electrons with Rashba spin-split bands, and any combination of multiple channels, including bulk parallel states in TI, which makes it useful in analyzing experimental results.

  8. A large-scale radiometric micro-quantitative complement fixation test for serum antibody titration

    International Nuclear Information System (INIS)

    A micro-quantitative complement fixation (CF) procedure based on 51Cr release is described. The method employs 50% hemolysis as end point and the alternation equation to calculate the amount of complement involved in the hemolytic reaction. Compared to the conventional CF tests, the radiometric procedure described here is very precise and consistently reproducible. Also, since only 3 4-fold dilutions of sera are used for the titration of antibodies over a wide range of concentrations, the test is very concise and is economical to perform. Its format is amenable to automation and computerization. This radioimetric CF procedure is thus most useful for large-scale immunological research and epidemiological surveilance studies. (Auth.)

  9. Potentiometric detection of chemical vapors using molecularly imprinted polymers as receptors

    OpenAIRE

    Rongning Liang; Lusi Chen; Wei Qin

    2015-01-01

    Ion-selective electrode (ISE) based potentiometric gas sensors have shown to be promising analytical tools for detection of chemical vapors. However, such sensors are only capable of detecting those vapors which can be converted into ionic species in solution. This paper describes for the first time a polymer membrane ISE based potentiometric sensing system for sensitive and selective determination of neutral vapors in the gas phase. A molecularly imprinted polymer (MIP) is incorporated into ...

  10. Potentiometric-level monitoring program - Mississippi and Louisiana: annual status report for fiscal year 1983

    International Nuclear Information System (INIS)

    Potentiometric-level data presented in this report were collected from October 1982 to September 1983 at 62 wells in Mississippi and Louisiana near Richton and Vacherie Domes, respectively. Six wells were added to the monitoring program during this period, and one previously measured well was damaged and has been deleted from the monitoring program. Analysis of the data indicates that most of the potentiometric-level changes recorded during fiscal year 1983 were small (less than 2 feet) and attributable to seasonal fluctuations. Of the 62 wells monitored, 18 exhibited potentiometric-level changes in excess of 2 feet. In Mississippi, the data generally indicate that a long-term, potentiometric-level increase is occurring in the Sparta, Kosciusko, Hattiesburg, Wilcox, and Citronelle Formations. Only seasonal fluctuations in potentiometric levels were observed in the caprock, and in the Catahoula and Cockfield Formations. In Louisiana, a long-term, potentiometric-level decline was observed for the Lower Austin Formation while an increase was observed for the Sparta and Upper Austin Formations. Seasonal fluctuations were observed in the Wilcox, Carrizo, and Nacatoch Formations. This work is a continuation of that described in ONWI-478 for fiscal year 1982. 24 references, 2 figures, 3 tables

  11. Complexometric titrations: new reagents and concepts to overcome old limitations.

    Science.gov (United States)

    Zhai, Jingying; Bakker, Eric

    2016-07-21

    Chelators and end point indicators are the most important parts of complexometric titrations. The most widely used universal chelator ethylenediamine tetraacetic acid (EDTA) and its derivatives can strongly coordinate with different metal ions. Their limited selectivity often requires the use of masking agents, and the multiple pKa values of the chelators necessitate a careful adjustment of pH during the procedure. Real world requirements for pH independent, selective and sensitive chelators and indicators call for a new design of these reagents. New concepts and structures of chelators and indicators have indeed recently emerged. We present here recent developments on chelators and indicators for complexometric titrations. Many of these advances were made possible only recently by moving the titration from a homogeneous to a heterogeneous phase using a new class of chelators and indicators based on highly selective ionophores embedded in ion-selective nanosphere emulsions. In view of achieving titrations in situ by complete instrumental control, thin layer electrochemistry has recently been shown to be an attractive concept that replaces the traditional cumbersome titration protocol with a direct reagent free sensing tool. PMID:27272695

  12. Reliability of home CPAP titration with different automatic CPAP devices

    Directory of Open Access Journals (Sweden)

    Lacasse Yves

    2008-07-01

    Full Text Available Abstract Background CPAP titration may be completed by automatic apparatus. However, differences in pressure behaviour could interfere with the reliability of pressure recommendations. Our objective was to compare pressure behaviour and effective pressure recommendations between three Automatic CPAP machines (Autoset Spirit, Remstar Auto, GK 420. Methods Sixteen untreated obstructive sleep apnea patients were randomly allocated to one of the 3 tested machines for a one-week home titration trial in a crossover design with a 10 days washout period between trials. Results The median pressure value was significantly lower with machine GK 420 (5.9 +/- 1.8 cm H2O than with the other devices both after one night and one week of CPAP titration (7.4 +/- 1.3 and 6.6 +/- 1.9 cm H2O. The maximal pressure obtained over the one-week titration was significantly higher with Remstar Auto (12.6 +/- 2.4 cm H2O, Mean +/- SD than with the two other ones (10.9 +/- 1.0 and 11.0 +/- 2.4 cm H2O. The variance in pressure recommendation significantly differed between the three machines after one night and between Autoset Spirit and the two other machines after 1 week. Conclusion Pressure behaviour and pressure recommendation significantly differ between Auto CPAP machines both after one night and one week of home titration.

  13. Library Automation

    OpenAIRE

    Dhakne, B. N.; Giri, V. V; Waghmode, S. S.

    2010-01-01

    New technologies library provides several new materials, media and mode of storing and communicating the information. Library Automation reduces the drudgery of repeated manual efforts in library routine. By use of library automation collection, Storage, Administration, Processing, Preservation and communication etc.

  14. Proton conducting ceramics for potentiometric hydrogen sensors for molten metals

    Energy Technology Data Exchange (ETDEWEB)

    Borland, H.; Llivina, L.; Colominas, S.; Abellà, J., E-mail: jordi.abella@iqs.edu

    2013-10-15

    Highlights: • Synthesis and chemical characterization of proton conductor ceramics. • Qualification of ceramics for hydrogen sensors in molten lithium–lead. • Ceramics have well-defined grains with a wide distribution of sizes. • Good agreement with predictions obtained with BaZrY, BaCeZrY and SrFeCo ceramics. -- Abstract: Tritium monitoring in lithium–lead eutectic (Pb–15.7Li) is of great importance for the performance of liquid blankets in fusion reactors. Also, tritium measurements will be required in order to proof tritium self-sufficiency in liquid metal breeding systems. On-line hydrogen (isotopes) sensors must be design and tested in order to accomplish these goals. Potentiometric hydrogen sensors for molten lithium–lead eutectic have been designed at the Electrochemical Methods Lab at Institut Quimic de Sarria (IQS) at Barcelona and are under development and qualification. The probes are based on the use of solid state electrolytes and works as proton exchange membranes (PEM). In this work the following compounds: BaZr{sub 0.9}Y{sub 0.1}O{sub 3}, BaCe{sub 0.6}Zr{sub 0.3}Y{sub 0.1}O{sub 3−α}, Sr(Ce{sub 0.6}-Zr{sub 0.4}){sub 0.9}Y{sub 0.1}O{sub 3−α} and Sr{sub 3}Fe{sub 1.8}Co{sub 2}O{sub 7} have been synthesized in order to be tested as PEM H-probes. Potentiometric measurements of the synthesized ceramic elements at 500 °C have been performed at a fixed hydrogen concentration. The sensors constructed using the proton conductor elements BaZr{sub 0.9}Y{sub 0.1}O{sub 3}, BaCe{sub 0.6}Zr{sub 0.3}Y{sub 0.1}O{sub 3−δ} and Sr{sub 3}Fe{sub 1.8}Co{sub 0.2}O{sub 7−δ} exhibited stable output potential and its value was close to the theoretical value calculated with the Nernst equation (deviation around 60 mV). In contrast, the sensor constructed using the proton conductor element Sr(Ce{sub 0.6}–Zr{sub 0.4}){sub 0.9}Y{sub 0.1}O{sub 3−δ} showed a deviation higher than 100 mV between experimental an theoretical data.

  15. Determination of fluoride with thorium nitrate by catalytic titration

    International Nuclear Information System (INIS)

    Amperometry, constant-current potentiometry and spectrophotometry were used to follow the course of catalytic titrations of fluoride and silicofluoride with thorium nitrate. The hydrogen peroxide-iodide system was used as the indicator reaction. Titrations were performed in 50% ethanolic acetate buffer, pH 3.6. Amounts of 3.70 to 6.85 mg of ammonium fluoride, 5.53 to 10.79 mg of potassium fluoride and 4.34 to 8.41 mg of sodium silicofluoride were determined with a maximum average deviation of 0.9%. The results obtained are in good agreement with those of comparable methods. (author)

  16. Titration procedures for nasal CPAP: Automatic CPAP or prediction formula?

    OpenAIRE

    HERTEGONNE, KATRIEN; Volna, J.; Portier, Sofie; De Pauw, Rebecca; Van Maele, Georges; Pevernagie, Dirk

    2008-01-01

    Background: The best method for titration Of continuous positive airway pressure (CPAP) therapy in obstructive sleep apnea (OSA) syndrome has not yet been established. The 90th or 95th percentiles of the pressure titrated over time by automatic CPAP (A-CPAP) have been recommended as reference for prescribing therapeutic fixed CPAP (F-CPAP). We compared A-CPAP to F-CPAP. which was determined by a common prediction formula. Methods: Forty-five patients who were habituated to F-CPAP underwent...

  17. Automatic potentiometric titration determination red wine total acidity%自动电位滴定法测定红葡萄酒总酸度

    Institute of Scientific and Technical Information of China (English)

    李艳霞; 宣亚文; 秦珠红; 常利平; 王小果

    2007-01-01

    测定红葡萄酒总酸度时,采用自动电位滴定法控制反应终点,避免了因指示剂使用而带来的误差,简化了操作步骤,提高了测定准确度,用于实际酒样的测定,结果满意.

  18. Automatic potentiometric titration determination content of the iron ore%自动电位滴定法测定铁矿石中全铁含量

    Institute of Scientific and Technical Information of China (English)

    李艳霞; 李敏; 谢红; 欧阳丽

    2008-01-01

    采用自动电位滴定法控制SnCl2还原Fe3+为Fe2+反应的终点,达到了准确控制SnCl2用量的目的,从而避免了剧毒试剂HgCl2的引入,节约了试荆,有效避免了环境污染.用于铁矿石中铁含量的测定,结果满意.

  19. Determination of Food Moisture by Automatic Potentiometric Titrator%全自动电位滴定仪测定食物水分

    Institute of Scientific and Technical Information of China (English)

    文娜; 宋良辉; 韦子昂

    2014-01-01

    通过对使用全自动电位滴定仪卡尔费休法测定食物水分的实验研究,建立了几种食物水分测定的方法,重现性好,操作方便快捷,减小了人为误差,可以推广使用.

  20. Bio-precipitation of uranium by two bacterial isolates recovered from extreme environments as estimated by potentiometric titration, TEM and X-ray absorption spectroscopic analyses

    Energy Technology Data Exchange (ETDEWEB)

    Merroun, Mohamed L., E-mail: merroun@ugr.es [Institute of Radiochemistry, Helmholtz Centre Dresden-Rossendorf, Dresden (Germany); Departamento de Microbiologia, Universidad de Granada, Campus Fuentenueva s/n 18071, Granada (Spain); Nedelkova, Marta [Institute of Radiochemistry, Helmholtz Centre Dresden-Rossendorf, Dresden (Germany); Ojeda, Jesus J. [Cell-Mineral Interface Research Programme, Kroto Research Institute, University of Sheffield, Broad Lane, Sheffield S3 7HQ (United Kingdom); Experimental Techniques Centre, Brunel University, Uxbridge, Middlesex UB8 3PH (United Kingdom); Reitz, Thomas [Institute of Radiochemistry, Helmholtz Centre Dresden-Rossendorf, Dresden (Germany); Fernandez, Margarita Lopez; Arias, Jose M. [Departamento de Microbiologia, Universidad de Granada, Campus Fuentenueva s/n 18071, Granada (Spain); Romero-Gonzalez, Maria [Cell-Mineral Interface Research Programme, Kroto Research Institute, University of Sheffield, Broad Lane, Sheffield S3 7HQ (United Kingdom); Selenska-Pobell, Sonja [Institute of Radiochemistry, Helmholtz Centre Dresden-Rossendorf, Dresden (Germany)

    2011-12-15

    Highlights: Black-Right-Pointing-Pointer Precipitation of uranium as U phosphates by natural bacterial isolates. Black-Right-Pointing-Pointer The uranium biomineralization involves the activity of acidic phosphatase. Black-Right-Pointing-Pointer Uranium bioremediation could be achieved via the biomineralization of U(VI) in phosphate minerals. - Abstract: This work describes the mechanisms of uranium biomineralization at acidic conditions by Bacillus sphaericus JG-7B and Sphingomonas sp. S15-S1 both recovered from extreme environments. The U-bacterial interaction experiments were performed at low pH values (2.0-4.5) where the uranium aqueous speciation is dominated by highly mobile uranyl ions. X-ray absorption spectroscopy (XAS) showed that the cells of the studied strains precipitated uranium at pH 3.0 and 4.5 as a uranium phosphate mineral phase belonging to the meta-autunite group. Transmission electron microscopic (TEM) analyses showed strain-specific localization of the uranium precipitates. In the case of B. sphaericus JG-7B, the U(VI) precipitate was bound to the cell wall. Whereas for Sphingomonas sp. S15-S1, the U(VI) precipitates were observed both on the cell surface and intracellularly. The observed U(VI) biomineralization was associated with the activity of indigenous acid phosphatase detected at these pH values in the absence of an organic phosphate substrate. The biomineralization of uranium was not observed at pH 2.0, and U(VI) formed complexes with organophosphate ligands from the cells. This study increases the number of bacterial strains that have been demonstrated to precipitate uranium phosphates at acidic conditions via the activity of acid phosphatase.

  1. Bio-precipitation of uranium by two bacterial isolates recovered from extreme environments as estimated by potentiometric titration, TEM and X-ray absorption spectroscopic analyses

    International Nuclear Information System (INIS)

    Highlights: ► Precipitation of uranium as U phosphates by natural bacterial isolates. ► The uranium biomineralization involves the activity of acidic phosphatase. ► Uranium bioremediation could be achieved via the biomineralization of U(VI) in phosphate minerals. - Abstract: This work describes the mechanisms of uranium biomineralization at acidic conditions by Bacillus sphaericus JG-7B and Sphingomonas sp. S15-S1 both recovered from extreme environments. The U–bacterial interaction experiments were performed at low pH values (2.0–4.5) where the uranium aqueous speciation is dominated by highly mobile uranyl ions. X-ray absorption spectroscopy (XAS) showed that the cells of the studied strains precipitated uranium at pH 3.0 and 4.5 as a uranium phosphate mineral phase belonging to the meta-autunite group. Transmission electron microscopic (TEM) analyses showed strain-specific localization of the uranium precipitates. In the case of B. sphaericus JG-7B, the U(VI) precipitate was bound to the cell wall. Whereas for Sphingomonas sp. S15-S1, the U(VI) precipitates were observed both on the cell surface and intracellularly. The observed U(VI) biomineralization was associated with the activity of indigenous acid phosphatase detected at these pH values in the absence of an organic phosphate substrate. The biomineralization of uranium was not observed at pH 2.0, and U(VI) formed complexes with organophosphate ligands from the cells. This study increases the number of bacterial strains that have been demonstrated to precipitate uranium phosphates at acidic conditions via the activity of acid phosphatase.

  2. "Titration simulator"--Good assistant for titration analysis%滴定分析教学的好帮手"Titration simulator"

    Institute of Scientific and Technical Information of China (English)

    屠婕红

    2005-01-01

    @@ Titration simulator(滴定模拟器)软件是专门为滴定分析而设计的教学软件,它短小精悍,简洁实用,可以从Internet网上免费下载,网址为:http://www.chemonline.net/Truechemsoft/downsoft.asp?softID=1565该软件所占容量仅为72KB,是学生训练及化学教师的好助手.笔者在教学中尝试运用该软件辅助教学,效果良好,现将Titration simulator软件的主要功能、应用简要介绍如下:

  3. Study on Determination of Titratable Acidity in Fruits Using Automatic Potentiometric Titrator%应用自动电位滴定仪测定水果中的可滴定酸

    Institute of Scientific and Technical Information of China (English)

    李文生; 冯晓元; 王宝刚; 郭振忠; 杨军军; 张长松

    2009-01-01

    应用自动电位滴定仪的等量等当点滴定法,测定苹果、葡萄、草莓三类水果样品的可滴定酸.结果表明加标回收率为92.85%~96.65%,相对标准偏差为0.64%~1.84%,不受浸提液的颜色影响,准确度和精密度高,可以在水果品质测定中推广.

  4. 自动电位滴定法和两相滴定法测定DDAG含量的比较%Comparison of DDAC Concentration Measured by Automatic Potentiometric Titration Procedure and Two-phase Titration Procedure

    Institute of Scientific and Technical Information of China (English)

    韩玉杰; 宋常明; 唐镇忠

    2008-01-01

    DDAC含量是评定ACQ防腐木材性能的一项重要指标,本文通过对比自动电位滴定法和两相滴定法测定防腐材萃取液中DDAC的含量,得出结论:采用自动电位滴定仪可大大缩短操作时间,提高了检测的准确度.

  5. Beer classification by means of a potentiometric electronic tongue.

    Science.gov (United States)

    Cetó, Xavier; Gutiérrez-Capitán, Manuel; Calvo, Daniel; del Valle, Manel

    2013-12-01

    In this work, an electronic tongue (ET) system based on an array of potentiometric ion-selective electrodes (ISEs) for the discrimination of different commercial beer types is presented. The array was formed by 21 ISEs combining both cationic and anionic sensors with others with generic response. For this purpose beer samples were analyzed with the ET without any pretreatment rather than the smooth agitation of the samples with a magnetic stirrer in order to reduce the foaming of samples, which could interfere into the measurements. Then, the obtained responses were evaluated using two different pattern recognition methods, principal component analysis (PCA), which allowed identifying some initial patterns, and linear discriminant analysis (LDA) in order to achieve the correct recognition of sample varieties (81.9% accuracy). In the case of LDA, a stepwise inclusion method for variable selection based on Mahalanobis distance criteria was used to select the most discriminating variables. In this respect, the results showed that the use of supervised pattern recognition methods such as LDA is a good alternative for the resolution of complex identification situations. In addition, in order to show an ET quantitative application, beer alcohol content was predicted from the array data employing an artificial neural network model (root mean square error for testing subset was 0.131 abv). PMID:23870992

  6. Process automation

    International Nuclear Information System (INIS)

    Process automation technology has been pursued in the chemical processing industries and to a very limited extent in nuclear fuel reprocessing. Its effective use has been restricted in the past by the lack of diverse and reliable process instrumentation and the unavailability of sophisticated software designed for process control. The Integrated Equipment Test (IET) facility was developed by the Consolidated Fuel Reprocessing Program (CFRP) in part to demonstrate new concepts for control of advanced nuclear fuel reprocessing plants. A demonstration of fuel reprocessing equipment automation using advanced instrumentation and a modern, microprocessor-based control system is nearing completion in the facility. This facility provides for the synergistic testing of all chemical process features of a prototypical fuel reprocessing plant that can be attained with unirradiated uranium-bearing feed materials. The unique equipment and mission of the IET facility make it an ideal test bed for automation studies. This effort will provide for the demonstration of the plant automation concept and for the development of techniques for similar applications in a full-scale plant. A set of preliminary recommendations for implementing process automation has been compiled. Some of these concepts are not generally recognized or accepted. The automation work now under way in the IET facility should be useful to others in helping avoid costly mistakes because of the underutilization or misapplication of process automation. 6 figs

  7. Modeling of titration experiments by a reactive transport model

    Institute of Scientific and Technical Information of China (English)

    Ma Hongyun; Samper Javier; Xin Xin

    2011-01-01

    Acid mine drainage (AMD) is commonly treated by neutralization with alkaline substances. This treatment is supported by titration experiments that illustrate the buffering mechanisms and estimate the base neutralization capacity (BNC) of the AMD. Detailed explanation of titration curves requires modeling with a hydro-chemical model. In this study the titration curves of water samples from the drainage of the As Pontes mine and the corresponding dumps have been investigated and six buffers are selected by analyzing those curves. Titration curves have been simulated by a reactive transport model to discover the detailed buffering mechanisms. These simulations show seven regions involving different buffering mechanism. The BNC is primarily from buffers of dissolved Fe, Al and hydrogen sulfate. The BNC can be approximated by: BNC = 3(CFe + CAl) + 0.05Csulfate, where the units are mol/L. The BNC of the sample from the mine is 9.25 × 10-3 mol/L and that of the dumps sample is 1.28 × 10-2 mol/L.

  8. Functionalized β-cyclodextrin based potentiometric sensor for naproxen determination.

    Science.gov (United States)

    Lenik, Joanna; Łyszczek, Renata

    2016-04-01

    Potentiometric sensors based on neutral β-cyclodextrins: (2-hydroxypropyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-benzoyl)-β-cyclodextrin and anionic β-cyclodextrin: (2-hydroxy-3-N,N,N-trimethylamino)propyl-β-cyclodextrin chloride for naproxen are described. Inclusion complexes of naproxen with the above-mentioned cyclodextrins were studied using IR spectroscopy. The electrode surface was made from PVC membranes doped with the appropriate β-cyclodextrin as ionophores and quaternary ammonium chlorides as positive charge additives that were dispersed in plasticizers. The optimum membrane contains heptakis(2,3,6-tri-O-benzoyl)-β-cyclodextrin, o-nitrophenyloctyl ether and tetraoctyl ammonium chloride as a lipophilic salt. The electrode is characterized by a Nernstian response slope of -59.0 ± 0.5 mV decade(-1) over the linear range of 5.0 × 10(-5)-1.0 × 10(-2) mol L(-1) and the detection limit 1.0 × 10(-5) mol L(-1), as well as the response time 10s. It can be used in the pH range 6.2-8.5 for 10 months without any considerable deterioration. Incorporation of β-cyclodextrins improved the electrode selectivity towards naproxen ions from several inorganic and organic interferents and some common drug excipients due to concovalent interactions (host molecule-guest molecule). The notable advantages of the naproxen-selective electrode include its high sensitivity, high selectivity, cost-effectiveness as well as accurate and comfortable application in drug analysis and milk samples. PMID:26838835

  9. Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Kivlehan, Francine [Tyndall National Institute, Lee Maltings, University College, Cork (Ireland); Mace, Wade J. [Tyndall National Institute, Lee Maltings, University College, Cork (Ireland); Department of Chemistry, Analytical and Biological Chemistry Research Facility, University College, Cork (Ireland); Moynihan, Humphrey A. [Department of Chemistry, Analytical and Biological Chemistry Research Facility, University College, Cork (Ireland); Arrigan, Damien W.M. [Tyndall National Institute, Lee Maltings, University College, Cork (Ireland)], E-mail: damien.arrigan@tyndall.ie

    2009-02-28

    Characterization of the interaction of a urea-functionalized calix[4]arene ionophore and phosphate was undertaken by combination of nuclear magnetic resonance (NMR) spectrometry, potentiometric selectivity coefficient evaluation and voltammetric ion transfer at the interface between two immiscible electrolyte solutions (ITIES). NMR revealed that the urea protons were involved in complexation with the target anion and potentiometric separate solution selectivity data indicated selectivity for phosphate over chloride and sulphate. Voltammetry at the ITIES confirmed that the ionophore-facilitated transfer of monohydrogen phosphate occurred in preference to dihydrogen phosphate transfer. The results correlate with previously reported data on the potentiometric evaluation of this calixarene as an anionophore in PVC-membrane electrodes. The data provide the basis for development of amperometric monohydrogen phosphate sensors based on the ion-transfer principle.

  10. Potentiometric measurement of glucose concentration with an immobilized glucose oxidase/catalase electrode.

    Science.gov (United States)

    Wingard, L B; Liu, C C; Wolfson, S K; Yao, S J; Drash, A L

    1982-01-01

    A series of enzyme electrodes for measurement of glucose have been constructed. The electrodes contain glucose oxidase immobilized on platinum, either with or without co-immobilization of catalase. When placed in buffered glucose, the enzyme electrodes show a potentiometric response to glucose with respect to a Ag/AgCl reference electrode. This response is reproducible in the physiologic range of glucose concentrations. The immobilization technique, some of the environmental variables such as oxygen concentration and pH, and several compounds that might interfere with the selectivity of the enzyme electrodes for glucose have received preliminary study. This direct potentiometric approach is undergoing further evaluation to determine the basic electrochemical mechanism responsible for the potentiometric signal and whether it can be adapted for continuous in vivo monitoring of the glucose concentration in body fluids. PMID:7172983

  11. Preparation of nano-structured Pt-YSZ composite and its application in oxygen potentiometric sensor

    International Nuclear Information System (INIS)

    Nano-structured Platinum-Yttria Stabilized Zirconia (YSZ) composites for oxygen potentiometric sensors were directly prepared with carbon black and the precursors such as chloroplatinic acid, zirconyl nitrate and yttrium nitrate. The as-prepared Pt-YSZ composite consisted of cubic crystalline YSZ and Pt particles, and the particle sizes of Pt catalyst and YSZ electrolyte were about 25-35 and 5-10 nm, respectively. The Pt-YSZ composite electrodes exhibited excellent electrochemical performances when evaluated by EIS measurements. The introduction of the nano-structured Pt-YSZ composite into the oxygen potentiometric sensor can reduce sensor's operating temperature to be about 380 deg. C, and also can reduce sensor's response time to be about 5 s at 400 deg. C. The oxygen potentiometric sensors incorporating nano-structured Pt-YSZ composites exhibited longer lifetime than those employing pure Pt as the sensing electrodes.

  12. Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation

    International Nuclear Information System (INIS)

    Characterization of the interaction of a urea-functionalized calix[4]arene ionophore and phosphate was undertaken by combination of nuclear magnetic resonance (NMR) spectrometry, potentiometric selectivity coefficient evaluation and voltammetric ion transfer at the interface between two immiscible electrolyte solutions (ITIES). NMR revealed that the urea protons were involved in complexation with the target anion and potentiometric separate solution selectivity data indicated selectivity for phosphate over chloride and sulphate. Voltammetry at the ITIES confirmed that the ionophore-facilitated transfer of monohydrogen phosphate occurred in preference to dihydrogen phosphate transfer. The results correlate with previously reported data on the potentiometric evaluation of this calixarene as an anionophore in PVC-membrane electrodes. The data provide the basis for development of amperometric monohydrogen phosphate sensors based on the ion-transfer principle

  13. The potentiometric and laser RAMAN study of the hydrolysis of uranyl chloride under physiological conditions and the effect of systematic and random errors on the hydrolysis constants

    International Nuclear Information System (INIS)

    The hydrolysis of uranyl ions in 0.15 mol/L (Na)C1 solution at 37 degrees Celsius has been studied by potentiometric titration. The results were consistent with the formation of (UO2)2(OH)2, (UO2)3(OH)4, (UO2)3(OH)5 and (UO2)4(OH)7. The stability constants, which were evaluated using a version of MINIQUAD, were found to be: log β22 = -5.693 ± 0.007, log β34 = -11.499 ± 0.024, log β35 = -16.001 ± 0.050, log β47 = -21.027 ± 0.051. Laser Raman spectroscopy has been used to identify the products including (UO2)4(OH)7 species. The difficulties in identifying the chemical species in solution and the effect of small errors on this selection has also been investigated by computer simulation. The results clearly indicate that small errors can lead to the selection of species that may not exist

  14. Potencialidades do dióxido de chumbo eletrodepositado como sensor potenciométrico Potentialities of electrodeposited lead dioxide as a potentiometric sensor

    Directory of Open Access Journals (Sweden)

    Milton Duffles Capelato

    1998-07-01

    Full Text Available This paper proposes an experiment to be performed in both instrumental analysis and experimental physical-chemistry curricular disciplines in order to open options to develop challenging basic research activities. Thus the experimental procedures and the results obtained in the preparation of electrodeposited lead dioxide onto graphite and its evaluation as potentiometric sensor for H3O+ and Pb2+ ions, are presented. The data obtained in acid-base titrations were compared with those of the traditional combination glass electrode at the same conditions. Although a linear sub-Nernstian response to free hydrogen ions was observed for the electrodeposited PbO2 electrode, a good agreement was obtained between them. Working as lead(II sensing electrode, the PbO2 showed a linear sub-Nernstian behavior at total Pb2+ concentrations ranging from 3,5 x 10-4 to 3,0 x 10-2 mol/L in nitrate media. For the redox couple PbO2/Pb(II the operational slope converges to the theoretical one, as the acidity of the working solution increases.

  15. Potentiometric Electronic Tongues for Foodstuff and Biosample Recognition—An Overview

    Directory of Open Access Journals (Sweden)

    Patrycja Ciosek

    2011-04-01

    Full Text Available Potentiometric sensors are attractive tools for the fabrication of various electronic tongues that can be used in wide area of applications, ranging from foodstuff recognition to environmental monitoring and medical diagnostics. Their main advantages are the ability to modify their selectivity (including cross-sensitivity effects and the possibility of miniaturization using appropriate construction methods for the transducer part (e.g., with the use of solid-state technology. In this overview various examples of the design, performance, and applications of potentiometric electronic tongues are presented. The results summarize recent research in the field conducted in the Department of Microbioanalytics, Warsaw University of Technology (WUT.

  16. Geostatistical analysis of potentiometric data in Wolfcamp aquifer of the Palo Duro Basin, Texas

    International Nuclear Information System (INIS)

    This report details a geostatistical analysis of potentiometric data from the Wolfcamp aquifer in the Palo Duro Basin, Texas. Such an analysis is a part of an overall uncertainty analysis for a high-level waste repository in salt. Both an expected potentiometric surface and the associated standard error surface are produced. The Wolfcamp data are found to be well explained by a linear trend with a superimposed spherical semivariogram. A cross-validation of the analysis confirms this. In addition, the cross-validation provides a point-by-point check to test for possible anomalous data

  17. Colloid Titration--A Rapid Method for the Determination of Charged Colloid.

    Science.gov (United States)

    Ueno, Keihei; Kina, Ken'yu

    1985-01-01

    "Colloid titration" is a volumetric method for determining charged polyelectrolytes in aqueous solutions. The principle of colloid titration, reagents used in the procedure, methods of endpoint detection, preparation of reagent solutions, general procedure used, results obtained, and pH profile of colloid titration are considered. (JN)

  18. Acidity titration curves - a versatile tool for the characterisation of acidic mine waste water

    International Nuclear Information System (INIS)

    Acidity titrations with NaOH are valuable tools for characterisation of acidic mine waters. - Titrations can be used to estimate metal concentrations. - Titrations can be carried out in the field, minimising changes in water chemistry due to sample handling time and procedure. (orig.)

  19. Titrating Polyelectrolytes - Variational Calculations and Monte Carlo Simulations

    CERN Document Server

    Jönsson, B; Peterson, C; Sommelius, O; Söderberg, B

    1995-01-01

    Variational methods are used to calculate structural and thermodynamical properties of a titrating polyelectrolyte in a discrete representation. The Coulomb interactions are emulated by harmonic repulsive forces, the force constants being used as variational parameters to minimize the free energy. For the titrating charges, a mean field approach is used. The accuracy is tested against Monte Carlo data for up to 1000 monomers. For an unscreened chain, excellent agreement is obtained for the end-to-end distance and the apparent dissociation constant. With screening, the thermodynamical properties are invariably well described, although the structural agreement deteriorates. A very simple rigid-rod approximation is also considered, giving surprisingly good results for certain properties.

  20. Determination of uranium by a gravimetric-volumetric titration method

    International Nuclear Information System (INIS)

    A volumetric-gravimetric modification of a method for the determination of uranium based on the reduction of uranium to U (IV) in a phosphoric acid medium and titration with a standard potassium dichromate solution is described. More than 99% of the stoichiometric amount of the titrating solution is weighed and the remainder is added volumetrically by using the Mettler DL 40 RC Memotitrator. Computer interconnected with analytical balances collects continually the data on the analyzed samples and evaluates the results of determination. The method allows to determine uranium in samples of uranium metal, alloys, oxides, and ammonium diuranate by using aliquot portions containing 30 - 100 mg of uranium with the error of determination, expressed as the relative standard deviation, of 0.02 - 0.05%. (author)

  1. Applications of isothermal titration calorimetry in protein science

    Institute of Scientific and Technical Information of China (English)

    Yi Liang

    2008-01-01

    During the past decade,isothermal titration calorimetry (ITC)has developed from a specialist method for understanding molecular interactions and other biological processes within cells to a more robust,widely used method.Nowadays,ITC is used to investigate all types of protein interactions,including protein-protein interactions,protein-DNA/RNA interactions,protein-small molecule interactions and enzyme kinetics;it provides a direct route to the complete thermodynamic characterization of protein interactions.This review concentrates on the new applications of ITC in protein folding and misfolding,its traditional application in protein interactions,and an overview of what can be achieved in the field of protein science using this method and what developments are likely to occur in the near future.Also,this review discusses some new developments of ITC method in protein science,such as the reverse titration of ITC and the displacement method of ITC.

  2. Monitoring assembly of ribonucleoprotein complexes by isothermal titration calorimetry

    OpenAIRE

    Recht, Michael I.; Ryder, Sean P.; Williamson, James R.

    2008-01-01

    Isothermal titration calorimetry (ITC) is a useful technique to study RNA-protein interactions, as it provides the only method by which the thermodynamic parameters of free energy, enthalpy, and entropy can be directly determined. This chapter presents a general procedure for studying RNA-protein interactions using ITC, and gives specific examples for monitoring the binding of Caenorhabditis elegans GLD-1 STAR domain to TGE RNA and the binding of Aquifex aeolicus S6:S18 ribosomal protein hete...

  3. Propagation and Titration of West Nile Virus on Vero Cells.

    Science.gov (United States)

    McAuley, Alexander J; Beasley, David W C

    2016-01-01

    The propagation and titration of viruses are key virological techniques. Unlike other flaviviruses, such as the dengue viruses, West Nile virus (WNV) grows and plaques very efficiently on Vero cells, usually inducing strong cytopathic effect (CPE) and forming clear plaques. Here, we outline the steps for propagating WNV from culture supernatant stocks and homogenized organ/mosquito samples, as well as for determining virus titers in samples by serial-dilution plaque assay using neutral red or crystal violet stains. PMID:27188547

  4. Titration of Human Coronaviruses Using an Immunoperoxidase Assay

    OpenAIRE

    Lambert, Francine; Jacomy, Helene; Marceau, Gabriel; J. Talbot, Pierre

    2008-01-01

    Calculation of infectious viral titers represents a basic and essential experimental approach for virologists. Classical plaque assays cannot be used for viruses that do not cause significant cytopathic effects, which is the case for strains 229E and OC43 of human coronavirus (HCoV). An alternative indirect immunoperoxidase assay (IPA) is herein described for the detection and titration of these viruses. Susceptible cells are inoculated with serial logarithmic dilutions of samples in a 96-wel...

  5. Electrochemical Pseudo-Titration of Water-Soluble Antioxidants

    OpenAIRE

    Tacchini, Philippe; Lesch, Andreas; Neequaye, Alice; Lagger, Grégoire; Liu, Jifeng; Cortes Salazar, Fernando; Girault, Hubert H.

    2013-01-01

    An amperometric test for the antioxidant power (AOP) of biological and food samples is presented. The gist of the method is to measure by linear sweep voltammetry the anodic current produced during the oxidation of the labile species present in the sample and then rationalizing this signal with a mathematical treatment that allows the pseudo-titration of antioxidants (AOs) around a given threshold potential. As a result, the AOP of the sample is calculated. This method allows the discriminati...

  6. Estimation of Lignin in Jute by Titration Method

    OpenAIRE

    M. Ashraf Hussain; M. Emdadul Huq; Sarder Matiur Rahman; Zakaria Ahmed

    2002-01-01

    The standard method for determining the Kappa Numbers of paper pulps has been evaluated, modified and applied for estimation of Lignin in different samples of jute. The values of the lignin content as determined from the Kappa Numbers of different samples of jute showed conformity with the values of Klason lignin estimated by sulphuric acid method. The method consisted in determining by titration the amount of potassium permanganate reduced by the lignin content of jute fibre. The developed m...

  7. In vitro titration of Theileria parva tick derived stabilates

    OpenAIRE

    Marcotty, T.; Speybroeck, N; Berkvens, D. (Dirk); Chaka, G.; Besa, R.; Madder, M.; Dolan, T.; Losson, B.; J. Brandt

    2004-01-01

    Immunization against the protozoan Theileria parva by infection and treatment has proved to be very efficient for the control of East Coast fever, an acute and often-fatal lymphoproliferative tick-borne disease of cattle in Eastern, Central and Southern Africa. The immunizing dose of live T. parva sporozoites used in this method is usually determined by in vivo titration. An alternative in vitro method of quantification of sporozoites in whole tick-derived stabilates is proposed. The method c...

  8. Predicting proton titration in cationic micelle and bilayer environments

    OpenAIRE

    Brian H. Morrow; Eike, David M.; Murch, Bruce P.; Koenig, Peter H.; Shen, Jana K.

    2014-01-01

    Knowledge of the protonation behavior of pH-sensitive molecules in micelles and bilayers has significant implications in consumer product development and biomedical applications. However, the calculation of pKa’s in such environments proves challenging using traditional structure-based calculations. Here we apply all-atom constant pH molecular dynamics with explicit ions and titratable water to calculate the pKa of a fatty acid molecule in a micelle of dodecyl trimethylammonium chloride and l...

  9. Potentiometric measurement of polymer-membrane electrodes based on lanthanum

    Energy Technology Data Exchange (ETDEWEB)

    Saefurohman, Asep, E-mail: saefurohman.asep78@Gmail.com; Buchari,, E-mail: saefurohman.asep78@Gmail.com; Noviandri, Indra, E-mail: saefurohman.asep78@Gmail.com [Department of Chemistry, Bandung Institute of Technology (Indonesia); Syoni [Department of Metallurgy Engineering, Bandung Institute of Technology (Indonesia)

    2014-03-24

    Quantitative analysis of rare earth elements which are considered as the standard method that has a high accuracy, and detection limits achieved by the order of ppm is inductively coupled plasma atomic emission spectroscopy (ICPAES). But these tools are expensive and valuable analysis of the high cost of implementation. In this study be made and characterized selective electrode for the determination of rare earth ions is potentiometric. Membrane manufacturing techniques studied is based on immersion (liquid impregnated membrane) in PTFE 0.5 pore size. As ionophores to be used tri butyl phosphate (TBP) and bis(2-etylhexyl) hydrogen phosphate. There is no report previously that TBP used as ionophore in polymeric membrane based lanthanum. Some parameters that affect the performance of membrane electrode such as membrane composition, membrane thickness, and types of membrane materials studied in this research. Manufacturing of Ion Selective Electrodes (ISE) Lanthanum (La) by means of impregnation La membrane in TBP in kerosene solution has been done and showed performance for ISE-La. FTIR spectrum results for PTFE 0.5 pore size which impregnated in TBP and PTFE blank showed difference of spectra in the top 1257 cm{sup −1}, 1031 cm{sup −1} and 794.7 cm{sup −1} for P=O stretching and stretching POC from group −OP =O. The result showed shift wave number for P =O stretching of the cluster (−OP=O) in PTFE-TBP mixture that is at the peak of 1230 cm{sup −1} indicated that no interaction bond between hydroxyl group of molecules with molecular clusters fosforil of TBP or R{sub 3}P = O. The membrane had stable responses in pH range between 1 and 9. Good responses were obtained using 10{sup −3} M La(III) internal solution, which produced relatively high potential. ISE-La showed relatively good performances. The electrode had a response time of 29±4.5 second and could be use for 50 days. The linear range was between 10{sup −5} and 10{sup −1} M.

  10. Potentiometric measurement of polymer-membrane electrodes based on lanthanum

    International Nuclear Information System (INIS)

    Quantitative analysis of rare earth elements which are considered as the standard method that has a high accuracy, and detection limits achieved by the order of ppm is inductively coupled plasma atomic emission spectroscopy (ICPAES). But these tools are expensive and valuable analysis of the high cost of implementation. In this study be made and characterized selective electrode for the determination of rare earth ions is potentiometric. Membrane manufacturing techniques studied is based on immersion (liquid impregnated membrane) in PTFE 0.5 pore size. As ionophores to be used tri butyl phosphate (TBP) and bis(2-etylhexyl) hydrogen phosphate. There is no report previously that TBP used as ionophore in polymeric membrane based lanthanum. Some parameters that affect the performance of membrane electrode such as membrane composition, membrane thickness, and types of membrane materials studied in this research. Manufacturing of Ion Selective Electrodes (ISE) Lanthanum (La) by means of impregnation La membrane in TBP in kerosene solution has been done and showed performance for ISE-La. FTIR spectrum results for PTFE 0.5 pore size which impregnated in TBP and PTFE blank showed difference of spectra in the top 1257 cm−1, 1031 cm−1 and 794.7 cm−1 for P=O stretching and stretching POC from group −OP =O. The result showed shift wave number for P =O stretching of the cluster (−OP=O) in PTFE-TBP mixture that is at the peak of 1230 cm−1 indicated that no interaction bond between hydroxyl group of molecules with molecular clusters fosforil of TBP or R3P = O. The membrane had stable responses in pH range between 1 and 9. Good responses were obtained using 10−3 M La(III) internal solution, which produced relatively high potential. ISE-La showed relatively good performances. The electrode had a response time of 29±4.5 second and could be use for 50 days. The linear range was between 10−5 and 10−1 M

  11. A titration microcalorimeter and the vesicle of mixed surfactants

    Institute of Scientific and Technical Information of China (English)

    白光月[1; 王玉洁[2; 王金本[3; 杨冠英[4; 韩布兴[5; 闫海科[6

    2000-01-01

    A titration microcalorimeter with the sample cells of 1 mL and 3 mL volume was constructed by combining LKB-2107 ampule microcalorimeter with an improved Thermometric titration microcalorimeter. Its sensitivity and precision were tested with the baseline noise and stability, the measurement of energy equivalent, and the linear relation of electric energy and integral area as the function of voltage (V)-time (f). Its accuracy was demonstrated by measuring the dilution enthalpy of a concentrated sucrose solution and the micelle-forming enthalpy of sodium dodecyl sulfate (SDS) in aqueous solution respectively. At the same time, the enthalpy of interaction between SDS and didodecyldimethylammonium bromide (DDAB) was measured by using the titration microcalorimeter, and the phase behavior of SDS-DDAB aqueous mixture was discussed. The microcalorimetric results show that the enthalpy of interaction between SDS and DDAB micelles is -29.53 kJ/mol, the enthalpy of formation of 1:1 SDS-DDAB salt is -125.8 kJ/mol,

  12. A titration microcalorimeter and the vesicle of mixed surfactants

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A titration microcalorimeter with the sample cells of 1 mL and 3 mL volume was constructed by combining LKB-2107 ampule microcalorimeter with an improved Thermometric titration microcalorimeter. Its sensitivity and precision were tested with the baseline noise and stability, the measurement of energy equivalent, and the linear relation of electric energy and integral area as the function of voltage (V )-time (t ). Its accuracy was demonstrated by measuring the dilution enthalpy of a concentrated sucrose solution and the micelle-forming enthalpy of sodium dodecyl sulfate (SDS) in aqueous solution respectively. At the same time, the enthalpy of interaction between SDS and didodecyldimethylammonium bromide (DDAB) was measured by using the titration microcalorimeter, and the phase behavior of SDS-DDAB aqueous mixture was discussed. The microcalorimetric results show that the enthalpy of interaction between SDS and DDAB micelles is ?29.53 kJ/mol, the enthalpy of formation of 1:1 SDS-DDAB salt is ?125.8 kJ/mol, the vesicle-forming enthalpy of SDS-DDAB is 41.23 kJ/mol, and the enthalpy of phase transition from vesicles to SDS rich micelle is 32.10 kJ/mol.

  13. Titrating and evaluating multi-drug regimens within subjects.

    Science.gov (United States)

    Shih, Margaret; Gennings, Chris; Chinchilli, Vernon M; Carter, Walter H

    2003-07-30

    The dosing of combination therapies is commonly undertaken empirically by practising physicians, and a coherent algorithm to approach the problem of combination dosing is currently lacking. Current methods of evaluating multiple drug combinations in clinical trials fail to provide information regarding the location of more effective doses when the combination is not found to differ from the standard, even though the absence of a difference does not necessarily mean the new combination is ineffective. Moreover, in studies where the new combination is found more effective, often a large proportion of the study participants obtain no benefit from the trial. Even with early stopping rules, the time these subjects spend on inferior treatments can have lasting detrimental effects, leading to problems with patient enrolment and adherence to study protocol. This paper describes an evolutionary operation (EVOP) direct-search procedure to titrate combination doses within individual patients. The Nelder-Mead simplex direct-search algorithm is used to titrate combinations of drugs within individual subjects. Desirability functions are utilized to define the main response of interest and additional responses or constraints. Statistical methodology for determining whether the titrated treatment combination has resulted in an improvement in subject response and for evaluating for therapeutic synergism is developed. Inferences can then be made about the efficacy of the combination or about the individual drugs that comprise the combination. The advantages of this approach include affording every patient the potential to benefit from the combination under study and permitting the consideration of multiple endpoints simultaneously. PMID:12854092

  14. BIOSENSOR FOR DIRECT DETERMINATION OF ORGANOPHOSPHATE NERVE AGENTS. 1. POTENTIOMETRIC ENZYME ELECTRODE. (R823663)

    Science.gov (United States)

    A potentiometric enzyme electrode for the direct measurement of organophosphate (OP)nerve agents was developed. The basic element of this enzyme electrode was a pH electrodemodified with an immobilized organophosphorus hydrolase (OPH) layer formed by cross-linkingOPH ...

  15. Potentiometric pH Measurements of Acidity Are Approximations, Some More Useful than Others

    Science.gov (United States)

    de Levie, Robert

    2010-01-01

    A recent article by McCarty and Vitz "demonstrating that it is not true that pH = -log[H+]" is examined critically. Then, the focus shifts to underlying problems with the IUPAC definition of pH. It is shown how the potentiometric method can provide "estimates" of both the IUPAC-defined hydrogen activity "and" the hydrogen ion concentration, using…

  16. Analysis of Lead and Zinc by Mercury-Free Potentiometric Stripping Analysis

    DEFF Research Database (Denmark)

    Andersen, Jens Enevold Thaulov

    1997-01-01

    A method is presented for trace-element analysis of lead and zinc by potentiometric stripping analysis (PSA) where both the glassy-carbon working electrode and the electrolyte are free of mercury. Analysis of zinc requires an activation procedure of the glassy-carbon electrode. The activation is...

  17. Interactions between oxovanadium (IV), glycylvaline and imidazoles: An aqueous potentiometric and spectroscopic study

    Indian Academy of Sciences (India)

    N Patel; V K Soni; K K Shukla; S Sharma; K B Pandeya

    2002-02-01

    Speciation has been determined in aqueous oxovanadium, glycylvaline and imidazoles at 25 ± 1° C and = 0.1M NaClO4 using a combination of potentiometry, and visible and EPR spectroscopy. Results of potentiometric and spectroscopic methods are consistent. Calculations of stability constants have been made using the SCOGS computer program.

  18. Reversible potentiometric oxygen sensors based on polymeric and metallic film electrodes.

    Science.gov (United States)

    Yim, H S; Meyerhoff, M E

    1992-09-01

    Various materials and sensor configurations that exhibit reversible potentiometric responses to the partial pressure of oxygen at room temperature in neutral pH solution are examined. In one arrangement, platinum electrodes are coated with plasticized poly(vinyl chloride) films doped with a cobalt(II) tetraethylene pentamine complex. For such sensors, potentiometric oxygen response is attributed to a mixed potential originating from the underlying platinum electrode surface as well as a change in redox potential of the Co(II)-tetren-doped film as the complex binds oxygen reversibly. The response due to the platinum surface is prolonged by the presence of the Co(II)-tetren/PVC film. Alternately, thin films of metallic copper, electrochemically deposited on platinum and/or sputtered or vapor deposited on a single crystal silicon substrate, may be used for reversible oxygen sensing. The long-term reversibility and potentiometric stability of such copper film-based sensors is enhanced (up to 1 month) by preventing the formation of cuprous oxide on the surfaces via the application of an external nonpolarizing cathodic current through the working electrode or by specifically using sputtered copper films that have [100] preferred crystal structures as determined by X-ray diffraction. The implications of these findings in relation to fabricating analytically useful potentiometric oxygen sensors are discussed. PMID:1416035

  19. Lead in Hair and in Red Wine by Potentiometric Stripping Analysis: The University Students' Design.

    Science.gov (United States)

    Josephsen, Jens

    1985-01-01

    A new program for training upper secondary school chemistry teachers (SE 537 693) depends heavily on student project work. A project in which lead in hair and in red wine was examined by potentiometric stripping analysis is described and evaluated. (JN)

  20. PVC Membrane Sensors for Potentiometric Determination of Acebutolol

    Directory of Open Access Journals (Sweden)

    Abdulrahman Al-Majed

    2007-12-01

    Full Text Available The construction and general performance characteristics of two novelpotentiometric membrane sensors responsive to the acebutolol are described. Thesensors are based on the use of ion-association complexes of acebutolol (AC withtetraphenylborate(TPB (I and phosphomolybdate(PM (II as exchange sites in a PVCmatrix. The sensors show a fast, stable and near- Nernstian for the mono charge cationof AC over the concentration range 1×10-3 - ~10-6 M at 25 °C over the pH range 2.0 -6.0 with cationic slope of 51.5 ± 0.5 and 53.0 ± 0.5 per concentration decade for AC-Iand AC-II sensors respectively. The lower detection limit is 6×10-6 M and 4×0-6 M withthe response time 20-30 s in the same order of both sensors. Selectivity coefficients ofAC related to a number of interfering cation and some organic compounds wereinvestigated. There are negligible interferences are caused by most of the investigatedspecies. The direct determination of 3 - 370 μg/ml of AC shows an average recovery of 99.4 and 99.5% and a mean relative standard deviation of 1 . 5 % at 100.0 μg/ml forsensor I and II respectively. The results obtained by determination of AC in tablets usingthe proposed sensors which comparable favorably with those obtained by the Britishpharmacopoeia method. In the present investigation the electrodes have been utilized asend point indicator for some precipitation titration reactions.

  1. Potentiometric-level monitoring program, Mississippi and Louisiana: Annual status report for fiscal year 1985

    International Nuclear Information System (INIS)

    Potentiometric-level data presented in this report were collected at 82 wells in Mississippi and Louisiana from October 1984 through September 1985. These wells are located near Richton and Cypress Creek Domes in Mississippi and Vacherie dome in Louisiana. Three wells were reinstated to the program during this period. Two previously destroyed wells were deleted from the program. Protective barriers were installed around 26 shallow borings in Mississippi. Cursory analysis of the data in Mississippi indicated minimal, if any, change in potentiometric level during the past year in the Citronelle, Hattiesburg, Cockfield, Sparta, and Wilcox Formations. A slight decline, on the order of 0.3 meter (1 foot), occurred during the past year in well MCCG-1, which is screened in the caprock of Cypress Creek Dome. The potentiometric level in well MRIG-9, in the caprock of Richton Dome, stabilized during fiscal year 1985 following 5 years of increase. The Catahoula Formation experienced a continuing decline of about 0.3 meter/year (1 foot/year). Well MH-5C, screened in the Cook Mountain Formation, showed a continuing, long-term, upward trend on the order of 1.5 meters (4.9 feet) during the past year. The potentiometric level of well MH-8C, screened in the Cook Mountain Formation, stabilized during fiscal year 1985, following 5 years of large annual increases. Wells screened in the Austin Formation in Louisiana showed a downward trend of 0.3 to 1 meter (1 to 3.3 feet) during fiscal year 1985. Other formations in Louisiana generally showed no change in potentiometric level

  2. Highly sensitive covalently functionalized light-addressable potentiometric sensor for determination of biomarker.

    Science.gov (United States)

    Liang, Jintao; Guan, Mingyuan; Huang, Guoyin; Qiu, Hengming; Chen, Zhengcheng; Li, Guiyin; Huang, Yong

    2016-06-01

    A biomarker is related to the biological status of a living organism and shows great promise for the early prediction of a related disease. Herein we presented a novel structured light-addressable potentiometric sensor (LAPS) for the determination of a model biomarker, human immunoglobulin G (hIgG). In this system, the goat anti-human immunoglobulin G antibody was used as recognition element and covalently immobilized on the surface of light-addressable potentiometric sensor chip to capture human immunoglobulin G. Due to the light addressable capability of light-addressable potentiometric sensor, human immunoglobulin G dissolved in the supporting electrolyte solution can be detected by monitoring the potential shifts of the sensor. In order to produce a stable photocurrent, the laser diode controlled by field-programmable gate array was used as the light emitter to drive the light-addressable potentiometric sensor. A linear correlation between the potential shift response and the concentration of human immunoglobulin G was achieved and the corresponding regression equation was ΔV (V)=0.00714ChIgG (μg/mL)-0.0147 with a correlation coefficient of 0.9968 over a range 0-150μg/mL. Moreover, the light-addressable potentiometric sensor system also showed acceptable stability and reproducibility. All the results demonstrated that the system was more applicable to detection of disease biomarkers with simple operation, multiple-sample format and might hold great promise in various environmental, food, and clinical applications. PMID:27040210

  3. Automation Security

    OpenAIRE

    Mirzoev, Dr. Timur

    2014-01-01

    Web-based Automated Process Control systems are a new type of applications that use the Internet to control industrial processes with the access to the real-time data. Supervisory control and data acquisition (SCADA) networks contain computers and applications that perform key functions in providing essential services and commodities (e.g., electricity, natural gas, gasoline, water, waste treatment, transportation) to all Americans. As such, they are part of the nation s critical infrastructu...

  4. Titratable acidity of beverages influences salivary pH recovery

    Directory of Open Access Journals (Sweden)

    Livia Maria Andaló TENUTA

    2015-01-01

    Full Text Available A low pH and a high titratable acidity of juices and cola-based beverages are relevant factors that contribute to dental erosion, but the relative importance of these properties to maintain salivary pH at demineralizing levels for long periods of time after drinking is unknown. In this crossover study conducted in vivo, orange juice, a cola-based soft drink, and a 10% sucrose solution (negative control were tested. These drinks differ in terms of their pH (3.5 ± 0.04, 2.5 ± 0.05, and 5.9 ± 0.1, respectively and titratable acidity (3.17 ± 0.06, 0.57 ± 0.04 and < 0.005 mmols OH- to reach pH 5.5, respectively. Eight volunteers with a normal salivary flow rate and buffering capacity kept 15 mL of each beverage in their mouth for 10 s, expectorated it, and their saliva was collected after 15, 30, 45, 60, 90, and 120 s. The salivary pH, determined using a mini pH electrode, returned to the baseline value at 30 s after expectoration of the cola-based soft drink, but only at 90 s after expectoration of the orange juice. The salivary pH increased to greater than 5.5 at 15 s after expectoration of the cola drink and at 30 s after expectoration of the orange juice. These findings suggest that the titratable acidity of a beverage influences salivary pH values after drinking acidic beverages more than the beverage pH.

  5. A titration model for evaluating calcium hydroxide removal techniques

    Directory of Open Access Journals (Sweden)

    Mark PHILLIPS

    2015-02-01

    Full Text Available Objective Calcium hydroxide (Ca(OH2 has been used in endodontics as an intracanal medicament due to its antimicrobial effects and its ability to inactivate bacterial endotoxin. The inability to totally remove this intracanal medicament from the root canal system, however, may interfere with the setting of eugenol-based sealers or inhibit bonding of resin to dentin, thus presenting clinical challenges with endodontic treatment. This study used a chemical titration method to measure residual Ca(OH2 left after different endodontic irrigation methods. Material and Methods Eighty-six human canine roots were prepared for obturation. Thirty teeth were filled with known but different amounts of Ca(OH2 for 7 days, which were dissolved out and titrated to quantitate the residual Ca(OH2 recovered from each root to produce a standard curve. Forty-eight of the remaining teeth were filled with equal amounts of Ca(OH2 followed by gross Ca(OH2 removal using hand files and randomized treatment of either: 1 Syringe irrigation; 2 Syringe irrigation with use of an apical file; 3 Syringe irrigation with added 30 s of passive ultrasonic irrigation (PUI, or 4 Syringe irrigation with apical file and PUI (n=12/group. Residual Ca(OH2 was dissolved with glycerin and titrated to measure residual Ca(OH2 left in the root. Results No method completely removed all residual Ca(OH2. The addition of 30 s PUI with or without apical file use removed Ca(OH2 significantly better than irrigation alone. Conclusions This technique allowed quantification of residual Ca(OH2. The use of PUI (with or without apical file resulted in significantly lower Ca(OH2 residue compared to irrigation alone.

  6. Lentiviral vectors titration using real-time PCR

    OpenAIRE

    Amir Allahverdi; Fatemeh Eskandari; Mohammad Hossein Moghadasi; Mehdi Azad; Mehdi Goudarzi; Saied Abroun; Masoud Soleimani

    2015-01-01

    Lentiviral vectors (LVs) are useful vehicle for genetransfer to dividing and non-dividing cells and genetic manipulations. However, the use of lentiviruses in studies requires an accurate titration technique.Quantitative real-time PCR (qPCR) is a sensitive technique for the indication and quantitation of retrovirals particles. In this study, we used the qPCR for lentiviral vector titeration. The puromycin resistance gene as templates for an SYBR green-based real-time qPCR method and detect le...

  7. ANALYSIS OF EFFLUENT FROM CAUSTIC TREATMENT PLANTS: IMPROVEMENT OF ACCURACY IN THE SIMULTANEOUS POTENTIOMETRIC DETERMINATION OF SULFIDE AND MERCAPTIDE IONS Análisis del efluente de una planta de tratamiento cáustico: mejoras de la precisión en la determinación simultánea potenciométrica de los iones de sulfuro y mercaptido

    Directory of Open Access Journals (Sweden)

    Marcio Reboucas

    2006-01-01

    Full Text Available Potentiometric titration using silver nitrate for determination of sulfide and mercaptide ions, as defined by the UOP Method 209, has been widely used for quality control of Spent Caustic Neutralization Unit in petroleum industries. However, it has been found this procedure does not provide accurate results for samples taken from units based on Wet Air Oxidation (WAO technology. Therefore, possible sources of error, such as concominant species, between-analytes interference and titration solvent, were investigated and adjustments in the method were proposed. Aqueous media should be used to prepare the titration solution instead of the recommended alcoholic solvent which was found to be related to the quite low analyte recoveries in WAO unit samples. The modified method can be successfully applied to samples with different chemical compositions which is the main advantage over the reference procedure. Limit of detection and relative standard deviation of 0,5 mg.L-1 and 5,2% for sulfide and 0,6 mg.L-1 and 5,5% for mercaptide were achieved.

  8. Infrared Turbidimetric Titration Method for Sulfate Ions in Brackish Water

    Directory of Open Access Journals (Sweden)

    Benabadji Nouredine

    2012-12-01

    Full Text Available In this work an infrared turbidimetric titration method is described for the determination of sulfate ions in brackish water. A suspension of barium sulfate is produced in an aqueous solution and/or brackish water sample by the addition of barium chloride solution and the turbidity is monitored with the help of an immersed infrared sensor. The developed sensor utilizes an optical system to measure the evolution of turbidity during the titration. This sensor is a simple device designed in the laboratory, consisting of two infrared diodes (LED, the first is an emitter and the second is used as detector (receiver. The data acquisition system is made with the help of a dataloger made on the basis of the microcontroller 16F877/874 accompanied with adaptable software both of them are self made. Concentration over 60 µg/mL of sulfate expressed as, SO42- can be measured with high reproducibility, by this method without a preliminary treatment or dilution of the sample. The method determines SO42 - concentration of brackish water with RSD of < 1.2%.

  9. A microfabrication-based approach to quantitative isothermal titration calorimetry.

    Science.gov (United States)

    Wang, Bin; Jia, Yuan; Lin, Qiao

    2016-04-15

    Isothermal titration calorimetry (ITC) directly measures heat evolved in a chemical reaction to determine equilibrium binding properties of biomolecular systems. Conventional ITC instruments are expensive, use complicated design and construction, and require long analysis times. Microfabricated calorimetric devices are promising, although they have yet to allow accurate, quantitative ITC measurements of biochemical reactions. This paper presents a microfabrication-based approach to integrated, quantitative ITC characterization of biomolecular interactions. The approach integrates microfabricated differential calorimetric sensors with microfluidic titration. Biomolecules and reagents are introduced at each of a series of molar ratios, mixed, and allowed to react. The reaction thermal power is differentially measured, and used to determine the thermodynamic profile of the biomolecular interactions. Implemented in a microdevice featuring thermally isolated, well-defined reaction volumes with minimized fluid evaporation as well as highly sensitive thermoelectric sensing, the approach enables accurate and quantitative ITC measurements of protein-ligand interactions under different isothermal conditions. Using the approach, we demonstrate ITC characterization of the binding of 18-Crown-6 with barium chloride, and the binding of ribonuclease A with cytidine 2'-monophosphate within reaction volumes of approximately 0.7 µL and at concentrations down to 2mM. For each binding system, the ITC measurements were completed with considerably reduced analysis times and material consumption, and yielded a complete thermodynamic profile of the molecular interaction in agreement with published data. This demonstrates the potential usefulness of our approach for biomolecular characterization in biomedical applications. PMID:26655185

  10. Measuring the Kinetics of Molecular Association by Isothermal Titration Calorimetry.

    Science.gov (United States)

    Vander Meulen, Kirk A; Horowitz, Scott; Trievel, Raymond C; Butcher, Samuel E

    2016-01-01

    The real-time power response inherent in an isothermal titration calorimetry (ITC) experiment provides an opportunity to directly analyze association kinetics, which, together with the conventional measurement of thermodynamic quantities, can provide an incredibly rich description of molecular binding in a single experiment. Here, we detail our application of this method, in which interactions occurring with relaxation times ranging from slightly below the instrument response time constant (12.5s in this case) to as large as 600s can be fully detailed in terms of both the thermodynamics and kinetics. In a binding titration scenario, in the most general case an injection can reveal an association rate constant (kon). Under more restrictive conditions, the instrument time constant-corrected power decay following each injection is simply an exponential decay described by a composite rate constant (kobs), from which both kon and the dissociation rate constant (koff) can be extracted. The data also support the viability of this exponential approach, for kon only, for a slightly larger set of conditions. Using a bimolecular RNA folding model and a protein-ligand interaction, we demonstrate and have internally validated this approach to experiment design, data processing, and error analysis. An updated guide to thermodynamic and kinetic regimes accessible by ITC is provided. PMID:26794355

  11. Spectrophotometric titrations: Application to the determination of some elements in uranium solutions

    International Nuclear Information System (INIS)

    The aim of this work is the application of spectrophotometric titrations to the analysis of uranium-containing solutions. We have been led to examine the general principles involved in these titrations, and we give a brief outline of these principles. In the first part we deal therefore with spectrophotometric titrations from a general point of view, examining their fundamental principle, their practical execution as well as the various possibilities of the method. The advantage of the titration are examined, in particular that of lending itself simultaneous determination of two species. The possibility of applying these spectrophotometric titrations to the analysis of uranium-containing solutions is the subject of the second part of this report: the dosage of a few species in uranium (VI) solutions is described. To this second part is added an experimental appendix consisting of a description of the apparatus, as well as of the operational techniques used for certain titrations, in particular those involving solutions containing uranium. (author)

  12. Comparison of VFA titration procedures used for monitoring the biogas process

    DEFF Research Database (Denmark)

    Lützhøft, Hans-Christian Holten; Boe, Kanokwan; Fang, Cheng;

    2014-01-01

    titration procedures. Currently, no standardized procedure is used and it is therefore difficult to compare the performance among plants. The aim of this study was to evaluate four titration procedures (for determination of VFA-levels of digested manure samples) and compare results with gas chromatographic...... (GC) analysis. Two of the procedures are commonly used in biogas plants and two are discussed in literature. The results showed that the optimal titration results were obtained when 40mL of four times diluted digested manure was gently stirred (200rpm). Results from samples with different VFA...... concentrations (1-11g/L) showed linear correlation between titration results and GC measurements. However, determination of VFA by titration generally overestimated the VFA contents compared with GC measurements when samples had low VFA concentrations, i.e. around 1g/L. The accuracy of titration increased when...

  13. 电镀废水中硫氰酸根离子含量的自动电位滴定%Determination of Thiocyanate Ions in Electroplating Wastewater by Automatic Potentiometeric Titration

    Institute of Scientific and Technical Information of China (English)

    姚晓华; 丘圣; 丘山; 丘星初

    2011-01-01

    The condition and method to determine thiocyanate ion by automatic potentiometric titration was studied. The results show that, the selection of silver electrode as indicator electrode, the electrode 217 with double liquid junction as reference, this method has high selectivity in nitric acid medium to titrate thiocyanate ion. When used in electroplating wastewater analysis, the method is simple and fast, which can print out the results in 4 minutes.%研究了用自动电位滴定测定硫氰酸根离子的条件和方法.实验结果表明,选用银电极为指示电极,217型双液接电极为参比电极,在硝酸介质中滴定硫氰酸根离子,方法具有高选择性;应用于电镀废水分析,方法简便快捷,在4min内能打印出分析结果.

  14. Potentiometric and polarographic studies on some aza styrene Schiff bases and their complexes with some lanthanide ions

    International Nuclear Information System (INIS)

    Potentiometric and polarographic studies have been carried out on some Schiff bases obtained by the condensation of o-hydroxybenylamine with salicyladehyde and some of its derivatives as well as their complexes have been determined potentiometrically by Bjerrum-Calvin method (Irving and Rossotti modification) and polarographically by Lingane method. Also the polarographic reduction of the Schiff bases was investigated in ethanolic-buffered solutions. A mechanism of the electrode reaction is proposed and discussed. (author). 10 refs., 2 figs., 3 tabs

  15. The effects of heated humidifier in continuous positive airway pressure titration

    OpenAIRE

    Yu, Chung-Chieh; Luo, Cheng-Ming; Liu, Yu-Chih; Wu, Huang-Pin

    2012-01-01

    Background Previous studies have shown that routine heated humidifier (HH) do not provide any benefit during continuous positive airway pressure (CPAP) titration if there are no significant naso-pharyngeal symptoms. In clinical practice, nasal diseases and upper airway symptoms are very common. This study investigates the effects of HH during CPAP titration in subjects with or without naso-pharyngeal symptoms. Methods Fifty-two patients who received polysomnography with CPAP titration were ra...

  16. Technical Note: How long can seawater oxygen samples be stored before titration?

    OpenAIRE

    Lankhorst, M.; Chavez, G; Nam, S. H.; Send, U.

    2014-01-01

    The concentration of dissolved oxygen in seawater is routinely measured using a standardized titration method that involves analysis shortly after the water sample has been collected. However, none of the existing procedural documents are specific about how soon after collection the titration has to be done. Here, we report on a small number of samples where duplicates were collected and one batch was titrated within days after collectio...

  17. Simple Modification of Karl-Fischer Titration Method for Determination of Water Content in Colored Samples

    OpenAIRE

    Eva Tavčar; Erika Turk; Samo Kreft

    2012-01-01

    The most commonly used technique for water content determination is Karl-Fischer titration with electrometric detection, requiring specialized equipment. When appropriate equipment is not available, the method can be performed through visual detection of a titration endpoint, which does not enable an analysis of colored samples. Here, we developed a method with spectrophotometric detection of a titration endpoint, appropriate for moisture determination of colored samples. The reaction takes p...

  18. Application of »Mass Titration« to Determination of Surface Charge of Metal Oxides

    OpenAIRE

    1998-01-01

    The mass titration method, used for the point of zero charge determination, was extended to the measurement of the surface charge density. The results agree with the common method, which is the acid-base titration of the colloidal suspension. The advantage of mass titration is that one does not need to perform blank titration, instead one simply adds metal oxide powder to the electrolyte aqueous solution of known pH. To cover the pH range above and below the point of zero charge, two experime...

  19. Disposable Miniaturized Screen‐Printed pH and Reference Electrodes for Potentiometric Systems

    DEFF Research Database (Denmark)

    Musa, Arnaud Emmanuel; del Campo, Francisco Javier; Abramova, Natalia;

    2011-01-01

    This work describes the development of a miniaturized potentiometric system comprising a miniaturized quasi‐reference electrode (QRE) coupled to a solid‐state ion‐selective electrode (ISE) for the monitoring of pH. We describe the optimization of materials and fabrication processes including screen‐printing...... (SP), electrode treatments (thermal and electrochemical) and the formulation and deposition of an ion‐selective membrane (ISM), to obtain a system compliant with biomedical specifications. We developed a potentiometric system composed of an Ag/AgCl QRE and a pH‐electrode (ISM deposited on a graphite...... electrode) that can be used continuously for a period of not less than 7 days in aqueous solutions. Curing the Ag/AgCl pastes during 20 minutes at 120 °C after printing allowed the QREs to display excellent potential stability, as demonstrated by an open‐circuit‐potential standard deviation of ±1.2 mV over...

  20. Challenges in the enantioanalysis of fucose using stochastic and potentiometric microsensors

    Directory of Open Access Journals (Sweden)

    Iuliana Moldoveanu

    2014-08-01

    Full Text Available Fucose gained significant interest in the medical field since a large number of studies have been reported on the role of fucose – as tumor marker. Electrochemical enantioselective sensors based on monocrystalline diamond paste and carbon paste working on stochastic and potentiometric modes were proposed for the enantioanalysis of fucose in biological fluids. Porphyrins and polymeric surfactants were used as modifiers for the diamond and carbon pastes in the design of sensors. Stochastic sensors were able to determine simultaneously l- and d-fucose in whole blood samples (qualitative and quantitative, and potentiometric sensors were used for quantitative determination of fucose in the biological fluids. The main advantages of the utilization of the proposed sensors were: real time enantioanalysis of fucose, no sample preparation for the biological fluid, and high reliability of the determinations.

  1. Geostatistical analysis of potentiometric data in the Pennsylvanian aquifer of the Palo Duro Basin, Texas

    International Nuclear Information System (INIS)

    This report details a geostatistical analysis of potentiometric data from the Pennsylvanian aquifer in the Palo Duro Basin, Texas. Such an analysis is a part of an overall uncertainty analysis for a high-level waste repository in salt. Both an expected potentiometric surface and the associated standard error surface are produced. The Pennsylvanian data are found to be well explained by a linear trend with a superimposed spherical semivariogram. A cross-validation of the analysis confirms this. In addition, the cross-validation provides a point-by-point check to test for possible anomalous data. The analysis is restricted to that portion of the Pennsylvanian aquifer that lies to the southwest of the Amarillo Uplift. The Pennsylvanian is absent is some areas across the uplift and data to the northeast were not used in this analysis. The surfaces produced in that analysis are included for comparison. 9 refs., 15 figs

  2. Nano Structured Potentiometric Sensors Based on Polyaniline Conducting Polymer for Determination of Cr (VI)

    Energy Technology Data Exchange (ETDEWEB)

    Mohammad-khah, Ali; Ansari, Reza; Delavar, Ali Fallah; Mosayebzadeh, Zahra [University of Guilan, Rasht (Iran, Islamic Republic of)

    2012-04-15

    In this paper, a potentiometric sensor based on polyaniline conducting polymer for potentiometric determination of Cr (VI) ions is reported. Polyaniline was synthesized electrochemically (cyclic voltammetry method) onto a micro pencil graphite electrode (0.7 mm diameter) in the presence of HCl and diphenylcarbazide (termed as (PGE/PAni/DPC). Some initial experiments were performed in order to find out the optimized conditions for preparation of the introduced Cr (VI) sensor electrode. The plot of E vs. log [Cr (VI)], showed a linear response in the range from 1.0 x 10{sup -6} to 1.0 x 10{sup -1} M. High repeatability with the detection limit of 8.0 x 10{sup -7} M was obtained

  3. Manganese(III) Porphyrin-based Potentiometric Sensors for Diclofenac Assay in Pharmaceutical Preparations

    OpenAIRE

    Eugenia Fagadar-Cosma; Vlad Chiriac; Elena Maria Pica; Luminita Nica; Liviu Calin Bolundut; Vasile Ostafe; Stela Pruneanu; Florina Pogacean; Liliana Olenic; Dana Vlascici

    2010-01-01

    Two manganese(III) porphyrins: manganese(III) tetraphenylporphyrin chloride and manganese(III)-tetrakis(3-hydroxyphenyl)porphyrin chloride were tested as ionophores for the construction of new diclofenac−selective electrodes. The electroactive material was incorporated either in PVC or a sol−gel matrix. The effect of different plasticizers and additives (anionic and cationic) on the potentiometric response was studied. The best results were obtained for the PVC membrane plasticized with dioct...

  4. Highly efficient potentiometric glucose biosensor based on functionalized InN quantum dots

    OpenAIRE

    Alvi, Naveed ul Hassan; Soto Rodríguez, Paul; Gómez Hernández, Víctor Jesús; Kumar, Praveen; Amin, G.; Nur, O; Willander, Magnus; Nötzel, R.

    2012-01-01

    We present a fast, highly sensitive, and efficient potentiometric glucose biosensor based on functionalized InN quantum-dots (QDs). The InN QDs are grown by molecular beam epitaxy. The InN QDs are bio-chemically functionalized through physical adsorption of glucose oxidase (GOD). GOD enzyme-coated InN QDs based biosensor exhibits excellent linear glucose concentration dependent electrochemical response against an Ag/AgCl reference electrode over a wide logarithmic glucose concentration range ...

  5. Potentiometric Urea Biosensor Based on an Immobilised Fullerene-Urease Bio-Conjugate

    OpenAIRE

    Kasra Saeedfar; Lee Yook Heng; Tan Ling Ling; Majid Rezayi

    2013-01-01

    A novel method for the rapid modification of fullerene for subsequent enzyme attachment to create a potentiometric biosensor is presented. Urease was immobilized onto the modified fullerene nanomaterial. The modified fullerene-immobilized urease (C60-urease) bioconjugate has been confirmed to catalyze the hydrolysis of urea in solution. The biomaterial was then deposited on a screen-printed electrode containing a non-plasticized poly(n-butyl acrylate) (PnBA) membrane entrapped with a hydrogen...

  6. Potentiometric Electronic Tongues for Foodstuff and Biosample Recognition—An Overview

    OpenAIRE

    Patrycja Ciosek; Wojciech Wróblewski

    2011-01-01

    Potentiometric sensors are attractive tools for the fabrication of various electronic tongues that can be used in wide area of applications, ranging from foodstuff recognition to environmental monitoring and medical diagnostics. Their main advantages are the ability to modify their selectivity (including cross-sensitivity effects) and the possibility of miniaturization using appropriate construction methods for the transducer part (e.g., with the use of solid-state technology). In this overvi...

  7. Potentiometric urea biosensor utilizing nanobiocomposite of chitosan-iron oxide magnetic nanoparticles

    OpenAIRE

    Ali, A.; AlSalhi, M. S.; Atif, M.; Ansari, Anees A.; Israr, Muhammad Qadir; Sadaf, J.R.; Ahmed, E; Nur, Omer; Willander, Magnus

    2013-01-01

    The iron oxide (Fe3O4) magnetic nanoparticles have been fabricated through a simple, cheap and reproducible approach. Scanning electron microscope, x-rays powder diffraction of the fabricated nanoparticles. Furthermore, the fabrication of potentiometric urea biosensor is carried out through drop casting the initially prepared isopropanol and chitosan solution, containing Fe3O4 nanoparticles, on the glass fiber filter with a diameter of 2 cm and a copper wire (of thickness −500 μm) has been ut...

  8. Redox potential of shallow groundwater by 1-month continuous in situ potentiometric measurements

    Science.gov (United States)

    Ioka, Seiichiro; Muraoka, Hirofumi; Suzuki, Yota

    2016-06-01

    One-month continuous in situ potentiometric measurements of redox potential (Eh) were used to investigate the dominant redox processes in the shallow groundwater (i.e., fit was found between measured Eh values and Eh values calculated using thermodynamic data of fine-grained goethite. This suggests that Fe redox system is related to the Eh values of shallow groundwater in the Aomori City aquifer.

  9. Optimal regional potentiometric surface design: least cost water supply/sustained groundwater yield

    OpenAIRE

    Peralta, R. C.; Killian, Paul J.

    1985-01-01

    A distributed parameter groundwater management model utilizing quadratic programming to develop an optimal regional steady-state potentiometric surface and its sustained groundwater withdrawal strategy is presented. It minimizes the regional cost of attempting to satisfy the water needs of each finite-difference cell (a) from groundwater and diverted surface water or (b) from groundwater and reduction of water needs achieved by reducing production acreages. Groundwater elevations, withdrawal ...

  10. Challenges in the enantioanalysis of fucose using stochastic and potentiometric microsensors

    OpenAIRE

    Iuliana Moldoveanu; Raluca-Ioana Stefan-van Staden; Constantina P. Kapnissi-Cristodoulou; Jacobus Frederick van Staden; Aboul-Enein, Hassan Y.

    2014-01-01

    Fucose gained significant interest in the medical field since a large number of studies have been reported on the role of fucose – as tumor marker. Electrochemical enantioselective sensors based on monocrystalline diamond paste and carbon paste working on stochastic and potentiometric modes were proposed for the enantioanalysis of fucose in biological fluids. Porphyrins and polymeric surfactants were used as modifiers for the diamond and carbon pastes in the design of sensors. Stochastic sens...

  11. Epidermal tattoo potentiometric sodium sensors with wireless signal transduction for continuous non-invasive sweat monitoring.

    Science.gov (United States)

    Bandodkar, Amay J; Molinnus, Denise; Mirza, Omar; Guinovart, Tomás; Windmiller, Joshua R; Valdés-Ramírez, Gabriela; Andrade, Francisco J; Schöning, Michael J; Wang, Joseph

    2014-04-15

    This article describes the fabrication, characterization and application of an epidermal temporary-transfer tattoo-based potentiometric sensor, coupled with a miniaturized wearable wireless transceiver, for real-time monitoring of sodium in the human perspiration. Sodium excreted during perspiration is an excellent marker for electrolyte imbalance and provides valuable information regarding an individual's physical and mental wellbeing. The realization of the new skin-worn non-invasive tattoo-like sensing device has been realized by amalgamating several state-of-the-art thick film, laser printing, solid-state potentiometry, fluidics and wireless technologies. The resulting tattoo-based potentiometric sodium sensor displays a rapid near-Nernstian response with negligible carryover effects, and good resiliency against various mechanical deformations experienced by the human epidermis. On-body testing of the tattoo sensor coupled to a wireless transceiver during exercise activity demonstrated its ability to continuously monitor sweat sodium dynamics. The real-time sweat sodium concentration was transmitted wirelessly via a body-worn transceiver from the sodium tattoo sensor to a notebook while the subjects perspired on a stationary cycle. The favorable analytical performance along with the wearable nature of the wireless transceiver makes the new epidermal potentiometric sensing system attractive for continuous monitoring the sodium dynamics in human perspiration during diverse activities relevant to the healthcare, fitness, military, healthcare and skin-care domains. PMID:24333582

  12. Schiff's Bases and Crown Ethers as Supramolecular Sensing Materials in the Construction of Potentiometric Membrane Sensors

    Directory of Open Access Journals (Sweden)

    Siavash Riahi

    2008-03-01

    Full Text Available Ionophore incorporated PVC membrane sensors are well-established analyticaltools routinely used for the selective and direct measurement of a wide variety of differentions in complex biological and environmental samples. Potentiometric sensors have someoutstanding advantages including simple design and operation, wide linear dynamic range,relatively fast response and rational selectivity. The vital component of such plasticizedPVC members is the ionophore involved, defining the selectivity of the electrodes' complexformation. Molecular recognition causes the formation of many different supramolecules.Different types of supramolecules, like calixarenes, cyclodextrins and podands, have beenused as a sensing material in the construction of ion selective sensors. Schiff's bases andcrown ethers, which feature prominently in supramolecular chemistry, can be used assensing materials in the construction of potentiometric ion selective electrodes. Up to now,more than 200 potentiometric membrane sensors for cations and anions based on Schiff'sbases and crown ethers have been reported. In this review cation binding and anioncomplexes will be described. Liquid membrane sensors based on Schiff's bases and crownethers will then be discussed.

  13. Stripping potentiometric analysis: application to determination of metallic cations in presence of uranium

    International Nuclear Information System (INIS)

    Potentiometric stripping analysis consists of a potentiostatic deposition step of trace elements and a subsequent stripping step. The trace metals are simultaneously reduced at a rotating electrode, the working electrode being a mercury film coated glassy carbon electrode; the amalgamated metals are then re-oxidized with an oxidizing agent. The analytical signal of this method is the time required for complete re-oxidation. Influence of different parameters on the analytical signal is studied by using mercury (II) ions as oxidizing agent in 5.10-4 M H2SO4 aqueous solution. Here, we point out the main characteristics of the potentiometric stripping analysis under the same experimental conditions. The reproductibility ranges are comprised between 0.5% to 1.5% and the detection limit for cadmium (II) is estimated to be 2.10-10 M with a plating time of 300 seconds. Small quantities, as 10-7 M Cd2+, Pb2+ and Zn2+ are simultaneously determined in presence of U (VI) ions (UO22+) with an accuracy of 0.5% for Cd2+ and Zn2+, and 4.5% for Pb2+. Compared to well-known electrochemical techniques, potentiometric stripping analysis appears to be a performing method for trace analysis in a wide range of media: this method permits the analysis of elements in presence of species more concentrated and being able to oxidize the trace elements

  14. Potentiometric detection of chemical vapors using molecularly imprinted polymers as receptors

    Science.gov (United States)

    Liang, Rongning; Chen, Lusi; Qin, Wei

    2015-07-01

    Ion-selective electrode (ISE) based potentiometric gas sensors have shown to be promising analytical tools for detection of chemical vapors. However, such sensors are only capable of detecting those vapors which can be converted into ionic species in solution. This paper describes for the first time a polymer membrane ISE based potentiometric sensing system for sensitive and selective determination of neutral vapors in the gas phase. A molecularly imprinted polymer (MIP) is incorporated into the ISE membrane and used as the receptor for selective adsorption of the analyte vapor from the gas phase into the sensing membrane phase. An indicator ion with a structure similar to that of the vapor molecule is employed to indicate the change in the MIP binding sites in the membrane induced by the molecular recognition of the vapor. The toluene vapor is used as a model and benzoic acid is chosen as its indicator. Coupled to an apparatus manifold for preparation of vapor samples, the proposed ISE can be utilized to determine volatile toluene in the gas phase and allows potentiometric detection down to parts per million levels. This work demonstrates the possibility of developing a general sensing principle for detection of neutral vapors using ISEs.

  15. Man-tailored biomimetic sensor of molecularly imprinted materials for the potentiometric measurement of oxytetracycline.

    Science.gov (United States)

    Moreira, Felismina T C; Kamel, Ayman H; Guerreiro, Joana R L; Sales, M Goreti F

    2010-10-15

    A novel biomimetic sensor for the potentiometric transduction of oxytetracycline is presented. The artificial host was imprinted in methacrylic acid and/or acrylamide based polymers. Different amounts of molecularly imprinted and non-imprinted polymers were dispersed in different plasticizing solvents and entrapped in a poly(vinyl chloride) matrix. Only molecularly imprinted based sensors allowed a potentiometric transduction, suggesting the existence of host-guest interactions. These sensors exhibited a near-Nernstian response in steady state evaluations; slopes and detection limits ranged 42-63 mV/decade and 2.5-31.3 μg/mL, respectively. Sensors were independent from the pH of test solutions within 2-5. Good selectivity was observed towards glycine, ciprofloxacin, creatinine, acid nalidixic, sulfadiazine, cysteine, hydroxylamine and lactose. In flowing media, the biomimetic sensors presented good reproducibility (RSD of ±0.7%), fast response, good sensitivity (65 mV/decade), wide linear range (5.0×10(-5) to 1.0×10(-2) mol/L), low detection limit (19.8 μg/mL), and a stable baseline for a 5×10(-3) M citrate buffer (pH 2.5) carrier. The sensors were successfully applied to the analysis of drugs and urine. This work confirms the possibility of using molecularly imprinted polymers as ionophores for organic ion recognition in potentiometric transduction. PMID:20688507

  16. Determination of Dimethylallylamine by Titration in Nonaqueous Solvent

    Institute of Scientific and Technical Information of China (English)

    LIU Li-hua; GONG Zhu-qing; ZHENG Ya-jie

    2004-01-01

    The content of dimethylallylamine was determined using glacial acetic acid as solvent, acetic-formic mixture as an anhydrite, perchloric acid-glacial acetic acid as titrant, and 1% crystal violet in acetic acid as indicator in the presence of methylamine and dimethylamine The influences of inert constituents and water on the titration were investigated, and a complete analytical method was determined. The results showed that the determination error of total amines increased with water increasing, while the effect of water on the determination of dimethylallylamine was little when the amount of water was within 5%, the relative error was generally within 1%, and that the end-point was acutely when about 10% chloroform was added. Compared with gas chromatography, this method is simple, convenient and accurate.

  17. Sailing on the "C": A Vitamin Titration with a Twist

    Science.gov (United States)

    Sowa, S.; Kondo, A. E.

    2003-05-01

    The experiment takes the traditional redox titration of vitamin C using iodine with starch as an indicator, and presents it to the student as a challenge in guided-inquiry format. Two versions, with different levels of difficulty, are provided, to accommodate students with varying levels of problem-solving skills. The "challenge" is both quantitative and qualitative: if you were an eighteenth-century sea captain packing for a voyage to the New World, would you take oranges, lemons, limes, or grapefruits to prevent your crew from getting scurvy? The challenge ties in history, nutrition, and health with chemistry, and provides students an opportunity to work with familiar food products in the laboratory.

  18. Automated Budget System

    Data.gov (United States)

    Department of Transportation — The Automated Budget System (ABS) automates management and planning of the Mike Monroney Aeronautical Center (MMAC) budget by providing enhanced capability to plan,...

  19. Design and construction of new potentiometric sensors for determination of Al3+ ion based on (Z)-2-(2-methyl benzylidene)-1-(2,4-dinitrophenyl) hydrazine.

    Science.gov (United States)

    Mizani, F; Salmanzadeh Ardabili, S; Ganjaliab, M R; Faridbod, F; Payehghadr, M; Azmoodeh, M

    2015-04-01

    (Z)-2-(2-methyl benzylidene)-1-(2,4-dinitrophenyl) hydrazine (L) was used as an active component of PVC membrane electrode (PME), coated graphite electrode (CGE) and coated silver wire electrode (CWE) for sensing Al(3+) ion. The electrodes exhibited linear Nernstian responses to Al(3+) ion in the concentration range of 1.0×10(-6) to 1.0×10(-1)M (for PME, LOD=8.8×10(-7)M), 5.5×10(-7) to 2.0×10(-1)M (for CWE, LOD=3.3×10(-7)M) and 1.5×10(-7) to 1.0×10(-1)M (for CGE, LOD=9.2×10(-8)M). The best performances were observed with the membranes having the composition of L:PVC:NPOE:NaTPB in the ratio of 5:35:57:3 (w/w; mg). The electrodes have a response time of 6s and an applicable pH range of 3.5-9.1. The sensors have a lifetime of about 15weeks and exhibited excellent selectivity over a number of mono-, bi-, and tri-valent cations including alkali, alkaline earth metal, heavy and transition metal ions. Analytical utility of the proposed sensor has been further tested by using it as an indicator electrode in the potentiometric titration of Al(3+) with EDTA. The electrode was also successfully applied for the determination of Al(3+) ion in real and pharmaceutical samples. PMID:25687018

  20. Potentiometric and spectrophotometric study of the stability of magnesium carbonate and bicarbonate ion pairs to 150 °C and aqueous inorganic carbon speciation and magnesite solubility

    Science.gov (United States)

    Stefánsson, Andri; Bénézeth, Pascale; Schott, Jacques

    2014-08-01

    The formation constants of magnesium bicarbonate and carbonate ion pairs have been experimentally determined in dilute hydrothermal solutions to 150 °C. Two experimental approaches were applied, potentiometric acid-base titrations at 10-60 °C and spectrophotometric pH measurements using two pH indicators, 2-naphthol and 4-nitrophenol, at 25 and 80-150 °C. At a given temperature, the first and second ionization constants of carbonic acid (K1, K2) and the ion pair formation constants for MgHCO3+(aq) (KMgHCO3+) and MgCO3(aq) (KMgCO3) were simultaneously fitted to the data. Results of this study compare well with previously determined values of K1 and K2. The formation constants of MgHCO3+(aq) and MgCO3(aq) ion pairs increased significantly with increasing temperature, with values of logKMgHCO3+ = 1.14 and 1.75 and of logKMgCO3 = 2.86 and 3.48 at 10 °C and 100 °C, respectively. These ion pairs are important aqueous species under neutral to alkaline conditions in moderately dilute to concentrated Mg-containing solutions, with MgCO3(aq) predominating over CO32-(aq) in solutions at pH >8. The predominance of magnesium carbonate over carbonate is dependent on the concentration of dissolved magnesium and the ratio of magnesium over carbonate. With increasing temperature and at alkaline pH, brucite solubility further reduced the magnesium concentration to levels below 1 mmol kg-1, thus limiting availability of Mg2+(aq) for magnesite precipitation.

  1. Surface complexation of neodymium at the rutile-water interface: A potentiometric and modeling study in NaCl media to 250°C

    Science.gov (United States)

    Ridley, Moira K.; Machesky, Michael L.; Wesolowski, David J.; Palmer, Donald A.

    2005-01-01

    The adsorption of Nd 3+ onto rutile surfaces was examined by potentiometric titration from 25 to 250°C, in 0.03 and 0.30 m NaCl background electrolyte. Experimental results show that Nd 3+ sorbs strongly, even at low temperature, with adsorption commencing below the pH znpc of rutile. In addition, there is a systematic increase in Nd 3+ adsorption with increasing temperature. The experimental results were rationalized and described using surface oxygen proton affinities computed from the MUlti SIte Complexation or MUSIC model, coupled with a Stern-based three-layer description of the oxide/water interface. Moreover, molecular-scale information was incorporated successfully into the surface complexation model, providing a unique geometry for the adsorption of Nd 3+ on rutile. The primary mode of Nd 3+ adsorption was assumed to be the tetradentate configuration found for Y 3+ adsorption on the rutile (110) surface from previously described in situ X-ray standing wave experiments, wherein the sorbing cations bond directly with two adjacent "terminal" and two adjacent "bridging" surface oxygen atoms. Similarly, the adsorption of Na + counterions was also assumed to be tetradentate, as supported by MD simulations of Na + interactions with the rutile (110) surface, and by analogous X-ray standing wave results for Rb + adsorption on rutile. Fitting parameters for Nd 3+ adsorption included binding constants for the tetradentate adsorption complex and capacitance values for the inner-sphere binding plane. In addition, hydrolysis of the tetradentate adsorption complex was permitted and resulted in significantly improved model fits at higher temperature and pH values. The modeling results indicate that the Stern-based MUSIC surface-complexation model adequately accommodates molecular-scale information to uniquely rationalize and describe multivalent ion adsorption systematically into the hydrothermal regime.

  2. 原位自动光度滴定法测定铁矿中铁含量%Study on application of photometric titration in the in situ determination of iron in iron ores

    Institute of Scientific and Technical Information of China (English)

    卢振国; 彭速标; 郑建国; 翟翠萍; 黄伟; 郭汉城; 邹振基

    2012-01-01

    利用自动电位滴定仪和DP5光度电极研究了原位自动光度滴定法在全铁测量中的应用.以HNO3、HCl和HF溶液为溶剂,采用密封微波消解系统分解试样.用NaOH溶液调节溶液酸度至pH 1.5,在原消解罐中以乙二胺四乙酸二钠盐(磺基水杨酸为指示剂)滴定铁.主要对滴定温度、试样的分解条件以及杂质对测定的干扰情况进行了研究.研究结果表明,称样量为0.05 g,溶剂为60%王水10 mL加1 mL HF(1 +99),温度为210℃,消解时间为20 min时溶样效果最好,50~60℃条件下,pH 1.5时进行滴定,结果准确可靠,能有效消除干扰.%The in situ determination of iron content in iron ores is presented with the automatic photometric titration method using an automatic potentiometric titrator and a DP5 photometric electrode. The samples are digested in closed vessels in a microwave oven with a mixture of nitric acid, hydrochloric acid and hydrofluoric acid solution. The resulting solution is diluted with water and adjusted to pHl. 5 with sodium hydroxide solution. Iron is determined in situ by automatic photometric titration with EDTA ( Sulfosalicylic acid as indicator). The conditions of titration temperature, sample decomposition and interferences are studied. The results show that optimal conditions are as follows, 0.05 g of samples, 10 mL of 60% aqua regia and 1 mL of (1+99) HF, digestion temperature of 210℃ , digestion time of 20 minutes, the titration solution at 50-60℃ and pH 1.5. The obtained results are accurate and reliable, and the interferences can be eliminated.

  3. A Laser-Pointer-Based Spectrometer for Endpoint Detection of EDTA Titrations

    Science.gov (United States)

    Dahm, Christopher E.; Hall, James W.; Mattioni, Brian E.

    2004-01-01

    A laser spectrometer for the ethylenediaminetetra-acetic acid (EDTA) titration of magnesium or calcium ions that is designed around a handheld laser pointer as the source and a photoresistor as the detector is developed. Findings show that the use of the spectrometer reduces the degree of uncertainty and error in one part of the EDTA titrations,…

  4. Effects of Acute and Chronic Cocaine Administration on Titrating-Delay Matching-to-Sample Performance

    Science.gov (United States)

    Kangas, Brian D.; Branch, Marc N.

    2012-01-01

    The effects of cocaine were examined under a titrating-delay matching-to-sample procedure. In this procedure, the delay between sample stimulus offset and comparison stimuli onset adjusts as a function of the subject's performance. Specifically, matches increase the delay and mismatches decrease the delay. Titrated delay values served as the…

  5. Humic substance charge determination by titration with a flexible cationic polyelectrolyte

    NARCIS (Netherlands)

    Tan, Wen-Feng; Norde, Willem; Koopal, Luuk K.

    2011-01-01

    The anionic charge of humic substances (HS) plays a major role in the interaction of HS with other components. Therefore, the potential of the polyelectrolyte titration technique to obtain the charge density of HS in simple 1-1 electrolyte solutions has been investigated. Titrations are carried out

  6. Humic substance charge determination by titration with a flexible cationic polyelectrolyte

    NARCIS (Netherlands)

    Tan, W.F.; Norde, W.; Koopal, L.K.

    2011-01-01

    The anionic charge of humic substances (HS) plays a major role in the interaction of HS with other components. Therefore, the potential of the polyelectrolyte titration technique to obtain the charge density of HS in simple 1–1 electrolyte solutions has been investigated. Titrations are carried out

  7. Quick titration of pergolide in cotreatment with domperidone is safe and effective

    NARCIS (Netherlands)

    Jansen, PAF; Herings, RMC; Samson, MM; Schuurmans-Daemen, LMPJ; Hovestadt, A; Verhaar, HJJ; Van Laar, T; de Vreede, P.

    2001-01-01

    The purpose of the study was to analyze efficacy and safety of quick pergolide titration combined with domperidone. In an open-label prospective study, pergolide was titrated in 16 days to a maximum of 3 mg/d doses as adjunctive treatment to L-Dopa in 10 elderly patients with Parkinson's disease. Si

  8. Manufacturing and automation

    OpenAIRE

    Ernesto Córdoba Nieto

    2010-01-01

    The article presents concepts and definitions from different sources concerning automation. The work approaches automation by virtue of the author’s experience in manufacturing production; why and how automation prolects are embarked upon is considered. Technological reflection regarding the progressive advances or stages of automation in the production area is stressed. Coriat and Freyssenet’s thoughts about and approaches to the problem of automation and its current state are taken and e...

  9. Development of potentiometric urea biosensor based on urease immobilized in PVA-PAA composite matrix for estimation of blood urea nitrogen (BUN).

    Science.gov (United States)

    Jha, Sandeep Kumar; Topkar, Anita; D'Souza, Stanislaus F

    2008-04-24

    A urea biosensor was developed using the urease entrapped in polyvinyl alcohol (PVA) and polyacrylamide (PAA) composite polymer membrane. The membrane was prepared on the cheesecloth support by gamma-irradiation induced free radical polymerization. The performance of the biosensor was monitored using a flow-through cell, where the membrane was kept in conjugation with the ammonia selective electrode and urea was added as substrate in phosphate buffer medium. The ammonia produced as a result of enzymatic reaction was monitored potentiometrically. The potential of the system was amplified using an electronic circuit incorporating operational amplifiers. Automated data acquisition was carried by connecting the output to a 12-bit analog to digital converter card. The sensor working range was 1-1000 mM urea with a response time of 120 s. The enzyme membranes could be reused 8 times with more than 90% accuracy. The biosensor was tested for blood urea nitrogen (BUN) estimation in clinical serum samples. The biosensor showed good correlation with commercial Infinitytrade mark BUN reagent method using a clinical chemistry autoanalyzer. The membranes could be preserved in phosphate buffer containing dithiothreitol, beta-mercaptoethanol and glycerol for a period of two months without significant loss of enzyme activity. PMID:18329719

  10. Predicting proton titration in cationic micelle and bilayer environments

    Energy Technology Data Exchange (ETDEWEB)

    Morrow, Brian H.; Shen, Jana K. [Department of Pharmaceutical Sciences, University of Maryland, Baltimore, Maryland 21201 (United States); Eike, David M.; Murch, Bruce P.; Koenig, Peter H. [Computational Chemistry, Modeling and Simulation GCO, Procter and Gamble, Cincinnati, Ohio 45201 (United States)

    2014-08-28

    Knowledge of the protonation behavior of pH-sensitive molecules in micelles and bilayers has significant implications in consumer product development and biomedical applications. However, the calculation of pK{sub a}’s in such environments proves challenging using traditional structure-based calculations. Here we apply all-atom constant pH molecular dynamics with explicit ions and titratable water to calculate the pK{sub a} of a fatty acid molecule in a micelle of dodecyl trimethylammonium chloride and liquid as well as gel-phase bilayers of diethyl ester dimethylammonium chloride. Interestingly, the pK{sub a} of the fatty acid in the gel bilayer is 5.4, 0.4 units lower than that in the analogous liquid bilayer or micelle, despite the fact that the protonated carboxylic group is significantly more desolvated in the gel bilayer. This work illustrates the capability of all-atom constant pH molecular dynamics in capturing the delicate balance in the free energies of desolvation and Coulombic interactions. It also shows the importance of the explicit treatment of ions in sampling the protonation states. The ability to model dynamics of pH-responsive substrates in a bilayer environment is useful for improving fabric care products as well as our understanding of the side effects of anti-inflammatory drugs.

  11. Predicting proton titration in cationic micelle and bilayer environments

    International Nuclear Information System (INIS)

    Knowledge of the protonation behavior of pH-sensitive molecules in micelles and bilayers has significant implications in consumer product development and biomedical applications. However, the calculation of pKa’s in such environments proves challenging using traditional structure-based calculations. Here we apply all-atom constant pH molecular dynamics with explicit ions and titratable water to calculate the pKa of a fatty acid molecule in a micelle of dodecyl trimethylammonium chloride and liquid as well as gel-phase bilayers of diethyl ester dimethylammonium chloride. Interestingly, the pKa of the fatty acid in the gel bilayer is 5.4, 0.4 units lower than that in the analogous liquid bilayer or micelle, despite the fact that the protonated carboxylic group is significantly more desolvated in the gel bilayer. This work illustrates the capability of all-atom constant pH molecular dynamics in capturing the delicate balance in the free energies of desolvation and Coulombic interactions. It also shows the importance of the explicit treatment of ions in sampling the protonation states. The ability to model dynamics of pH-responsive substrates in a bilayer environment is useful for improving fabric care products as well as our understanding of the side effects of anti-inflammatory drugs

  12. 沉淀滴定的林邦滴定曲线方程%Ringbom titration curve equation of precipitation titration

    Institute of Scientific and Technical Information of China (English)

    乔成立; 李文新

    2014-01-01

    Ionic strength effect,acid effect,precipitation effect and ligand effect were identified as side reactions of the main reaction,Ringbom titration curve equation of precipitation titration was derived by means of material balance, conditional stability constant and titration scores,etc,which can lay a solid foundation for researching precipitation titration analysis theory on the basis of Ringbom titration curve equation.%把离子强度效应、酸效应、沉淀效应、配位效应等看作是主反应发生的副反应,通过物料平衡、条件稳定常数和滴定分数等推导出沉淀滴定的林邦滴定曲线方程,为用林邦滴定曲线方程研究沉淀滴定分析理论打下坚实的基础。

  13. Fusion of Potentiometric & Voltammetric Electronic Tongue for Classification of Black Tea Taste based on Theaflavins (TF) Content

    Science.gov (United States)

    Bhattacharyya, Nabarun; Legin, Andrey; Papieva, Irina; Sarkar, Subrata; Kirsanov, Dmitry; Kartsova, Anna; Ghosh, Arunangshu; Bandyopadhyay, Rajib

    2011-09-01

    Black tea is an extensively consumed beverage worldwide with an expanding market. The final quality of black tea depends upon number of chemical compounds present in the tea. Out of these compounds, theaflavins (TF), which is responsible for astringency in black tea, plays an important role in determining the final taste of the finished black tea. The present paper reports our effort to correlate the theaflavins contents with the voltammetric and potentiometric electronic tongue (e-tongue) data. Noble metal-based electrode array has been used for collecting data though voltammetric electronic tongue where as liquid filled membrane based electrodes have been used for potentiometric electronic tongue. Black tea samples with tea taster score and biochemical results have been collected from Tea Research Association, Tocklai, India for the analysis purpose. In this paper, voltammetric and potentiometric e-tongue responses are combined to demonstrate improvement of cluster formation among tea samples with different ranges of TF values.

  14. Improved Performance of the Potentiometric Biosensor for the Determination of Creatinine

    DEFF Research Database (Denmark)

    Andersen, Jens Enevold Thaulov; Rasmussen, Claus/Dallerup; Zachau-Christiansen, Birgit

    2007-01-01

    The development of potentiometric biosensors for the determination of creatinine is attractive because it is a frequently analysed species in clinical chemistry. Contemporary methods of analysing creatinine engage chemicals harmful to the environment and generate large volumes of waste disposals...... revisited and optimised with respect to repeatability, sensitivity, limit of detection (LOD) and response time. A detection limit of 0.3 M and a sensitivity of 58.78 ± 0.03 mV (23.5 0C) were obtained in tris buffer at pH = 7.4 after introduction of shielding of all electronics and software filtering...

  15. Direct Potentiometric Determination of Penicillamine in Real Samples by Using Copper ISE

    OpenAIRE

    Vukušić, Tina; Prkić, Ante; Giljanović, Josipa; Sokol, Vesna; Bošković, Perica

    2015-01-01

    Direct potentiometric method for determination of penicillamine in pharmaceuticals by using commercial copper ISE is described. Proposed method is very inexpensive, simple and reasonably fast method for determination of Pen in acetic buffer, pH = 4 without pretreatment of pharmaceuticals. Determination is based on the reaction between Pen and Cu2+ from electrode membrane. Described method has linear response range for Pen from 2×10−6 to 1×10−2 mol L−1 with limit of detection of 1.1×10−6 mol L...

  16. Development of miniaturized potentiometric nitrate- and ammonium selective electrodes for applications in water monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Schwarz, J.; Kaden, H. [Kurt-Schwabe-Institut fuer Mess- und Sensortechnik e.V., Meinsberg (Germany); Pausch, G. [Umwelt- und Ingenieurtechnik GmbH, Dresden (Germany)

    2000-06-01

    Mobile analysis with potentiometric sensors is well suited for field measurements. Ion-selective electrodes (ISE) based on polymeric membranes for in-situ determination of nitrate and ammonium contents in ground water, drinking water and surface water have been developed. The ISE are integrated in a multisensor module (MSM) for monitoring these ions over longer time intervals. The receptor is a PVC-membrane with tridodecylammonium nitrate (TDDA) for nitrate- and nonactine for ammonium-electrodes as ionophores. As plasticizer dibutylphthalate (DBT) was used. The main parameters for assessing the efficiency of these ISE are presented. (orig.)

  17. Thermodynamics of micellization of N-alkylpyridinium chlorides: a potentiometric study:

    OpenAIRE

    Simončič, Barbara; Špan, Jože

    1998-01-01

    The critical micelle concentration (CMC) and the thermodynamics functions deltaG° mic, deltaH° mic and deltaS° mic for the micellization process of the two pyridinium cationic surfactants N-dodecilpiridinium chloride (DPC) in aqueous solution were studied by a potentiometric method using surfactant cation-sensitive membrane electrodes. The e.m.f. of the galvanic cell was measured as a function of surfactant concentration at temperatures of 15, 25, 35 and 45 °C at different concentrations of a...

  18. Indicator electrodes from d-elements for application in different types of potentiometric analytical methods

    OpenAIRE

    Z. Kunasheva; Dina Mendalieva; B. Seifullina

    2012-01-01

    The article covers the use of metal electrodes from titanium, tungsten, molybdenum as indicator electrodes at potentiometric method of analysis. The condition of measuring operation in dependence on pH, ionic strength of solutions is described in the article. Electrode potential of testing electrodes are measured in the interval of concentration of salts from 0,1∙10-1 mole/l till 0,1∙10-6 mole/l. The results of testing of electrical-analytical description of metal electrodes made of d-element...

  19. Complexation of Iron by Dopamine Analogs; A Spectrophotometric and Potentiometric Study

    OpenAIRE

    *T. Fiaz; N. Fatima; S. Z. A. Zaidi

    2013-01-01

    The chelation of Bio-essential metal, Iron, with dopamine analogs was studied at 30±2°C. Fe2+ formed intense color complex with these molecules with an absorbance maxima in visible region. A distinct peak of Fe-Carbidopa complex at 364nm with molar absorptivity of 1600 M-1 cm-1 was observed while that of Fe-Levodopa and Fe-Methyldopa were observed at 730nm with molar absorptivities of 306 M-1 cm-1 and 2300 M-1 cm-1, respectively. Potentiometric studies of the complex indicate that Fe(II) ...

  20. Structural characterization of hexadecyltrimethylammonium-smectite composites and their potentiometric electrode applications

    Energy Technology Data Exchange (ETDEWEB)

    Cubuk, Osman [Department of Chemistry, Faculty of Arts and Sciences, Erzincan University, 24100 Erzincan (Turkey); Caglar, Bulent, E-mail: bcaglar55@gmail.com [Department of Chemistry, Faculty of Arts and Sciences, Erzincan University, 24100 Erzincan (Turkey); Topcu, Cihan; Coldur, Fatih; Sarp, Gokhan [Department of Chemistry, Faculty of Arts and Sciences, Erzincan University, 24100 Erzincan (Turkey); Tabak, Ahmet [Department of Chemistry, Faculty of Arts and Sciences, Recep Tayyip Erdoğan University, 53100 Rize (Turkey); Sahin, Erdal [Department of Chemistry, Faculty of Arts and Sciences, Erzincan University, 24100 Erzincan (Turkey)

    2015-05-30

    Graphical abstract: - Highlights: • Surfactant cations intercalated with different molecular arrangements into smectite layers. • The electrophoretic mobility values indicate that excess surfactant loadings also create positive charges on the organosmectites surfaces. • A novel potentiometric SCN{sup −} selective electrode was fabricated based on modified smectite. - Abstract: Organosmectites were prepared by the intercalation of hexadecyltrimethylammonium cations at various ratios into interlayer of Unye smectite. Structural, thermal, morphological and textural properties of the synthesized organosmectites were characterized. Afterwards, a novel potentiometric PVC-membrane thiocyanate selective electrode was prepared based on the obtained hexadecyltrimethylammonium modified smectites as electroactive material. The basal spacing values of organosmectites were observed in the range of 15.61 and 35.50 Å. Powder X-ray diffraction data show that the surfactant cations penetrated into the smectite layers with different molecular arrangements. Modification of smectite with hexadecyltrimethylammonium led to appreciable decreases in the intensities of the FTIR bands at 3402 and 1635 cm{sup −1} and the new characteristic vibrational bands at 2927, 2850, 1472 and 722 cm{sup −1} originating from the surfactant molecules appeared. The thermal analysis data showed that the decomposition of surfactant species occurred in the temperature range of 170–720 °C and the amount of dehydrated water gradually decreased with the increase in surfactant amount. The intercalation of surfactant species within the gallery spacing led gradually to smaller surface areas. In addition, the electrophoretic mobility values indicate that excess surfactant loadings also generate positive charges on the organosmectite surfaces. The most convenient membrane composition resulting in the best potentiometric performance was investigated. The optimum membrane composition was determined to

  1. Underground Test Area Subproject Phase I Data Analysis Task. Volume II - Potentiometric Data Document Package

    Energy Technology Data Exchange (ETDEWEB)

    None

    1996-12-01

    Volume II of the documentation for the Phase I Data Analysis Task performed in support of the current Regional Flow Model, Transport Model, and Risk Assessment for the Nevada Test Site Underground Test Area Subproject contains the potentiometric data. Because of the size and complexity of the model area, a considerable quantity of data was collected and analyzed in support of the modeling efforts. The data analysis task was consequently broken into eight subtasks, and descriptions of each subtask's activities are contained in one of the eight volumes that comprise the Phase I Data Analysis Documentation.

  2. Potentiometric study of polyaniline film synthesized with various dopants and composite-dopant: A comparative study

    Indian Academy of Sciences (India)

    P D Gaikwad; D J Shirale; V K Gade; P A Savale; K P Kakde; H J Kharat; M D Shirsat

    2006-08-01

    The potentiometric study of polyaniline (PANI) film synthesized with dopants viz. polyvinyl sulfonic acid (PVS), -toluene sulfonic acid (TS), dodecyl benzene sulfonic acid (DBS) and composite-dopants viz. PVS–TS and PVS–DBS, has been carried out. The synthesized PANI films were characterized by electrochemical technique, UV-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and conductivity measurement. It was found that the PANI doped with PVS gives good electrochemical properties, conductivity as well as surface morphology as compared to TS and DBS, whereas in composite dopants the PANI doped with PVS–TS gives good polymer matrix as compared to PVS–DBS.

  3. Structural characterization of hexadecyltrimethylammonium-smectite composites and their potentiometric electrode applications

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Surfactant cations intercalated with different molecular arrangements into smectite layers. • The electrophoretic mobility values indicate that excess surfactant loadings also create positive charges on the organosmectites surfaces. • A novel potentiometric SCN− selective electrode was fabricated based on modified smectite. - Abstract: Organosmectites were prepared by the intercalation of hexadecyltrimethylammonium cations at various ratios into interlayer of Unye smectite. Structural, thermal, morphological and textural properties of the synthesized organosmectites were characterized. Afterwards, a novel potentiometric PVC-membrane thiocyanate selective electrode was prepared based on the obtained hexadecyltrimethylammonium modified smectites as electroactive material. The basal spacing values of organosmectites were observed in the range of 15.61 and 35.50 Å. Powder X-ray diffraction data show that the surfactant cations penetrated into the smectite layers with different molecular arrangements. Modification of smectite with hexadecyltrimethylammonium led to appreciable decreases in the intensities of the FTIR bands at 3402 and 1635 cm−1 and the new characteristic vibrational bands at 2927, 2850, 1472 and 722 cm−1 originating from the surfactant molecules appeared. The thermal analysis data showed that the decomposition of surfactant species occurred in the temperature range of 170–720 °C and the amount of dehydrated water gradually decreased with the increase in surfactant amount. The intercalation of surfactant species within the gallery spacing led gradually to smaller surface areas. In addition, the electrophoretic mobility values indicate that excess surfactant loadings also generate positive charges on the organosmectite surfaces. The most convenient membrane composition resulting in the best potentiometric performance was investigated. The optimum membrane composition was determined to have 20.0% (w/w) 2

  4. Integrated potentiometric detector for use in chip-based flow cells

    Science.gov (United States)

    Tantra; Manz

    2000-07-01

    A new kind of potentiometric chip sensor for ion-selective electrodes (ISE) based on a solvent polymeric membrane is described. The chip sensor is designed to trap the organic cocktail inside the chip and to permit sample solution to flow past the membrane. The design allows the sensor to overcome technical problems of ruggedness and would therefore be ideal for industrial processes. The sensor performance for a Ba2+-ISE membrane based on a Vogtle ionophore showed electrochemical behavior similar to that observed in conventional electrodes and microelectrode arrangements. PMID:10905321

  5. Analysis of Lead and Zinc by Mercury-Free Potentiometric Stripping Analysis

    DEFF Research Database (Denmark)

    Andersen, Jens Enevold Thaulov

    1997-01-01

    A method is presented for trace-element analysis of lead and zinc by potentiometric stripping analysis (PSA) where both the glassy-carbon working electrode and the electrolyte are free of mercury. Analysis of zinc requires an activation procedure of the glassy-carbon electrode. The activation is...... performed by pre-concentrating zinc on glassy carbon at -1400 mV(SCE) in a mercury-free electrolyte containing 0.1 M HCl and 2 ppm Zn2+, followed by stripping at approx. -1050 mV. A linear relationship between stripping peak areas, recorded in the derivative mode, and concentration was found in the...

  6. Potentiometric sensor fabrication having 2D sarcosine memories and analytical features.

    Science.gov (United States)

    Özkütük, Ebru Birlik; Diltemiz, Sibel Emir; Avcı, Şeyma; Uğurağ, Deniz; Aykanat, Rabia Berna; Ersöz, Arzu; Say, Rıdvan

    2016-12-01

    In this study, a simple, rapid and sensitive method based on novel molecular imprinted polymeric sensor has been developed and validated for the determination of prostate cancer metabolite biomarker. The molecularly imprinted polymer (MIP) has been synthesized by emulsion polymerization, using sarcosine as template molecule, methacryloylamido histidine (MAH) as functional monomer and ethylene glycol dimethacrylate (EDMA) as cross-linking agent. The performance of the developed sarcosine sensor has been evaluated, and the results have indicated that a sensitive potentiometric sensor has been fabricated. The sarcosine sensor has showed high-selectivity, shorter response time (5.5months). PMID:27612708

  7. On the Physical Meaning of the Isothermal Titration Calorimetry Measurements in Calorimeters with Full Cells

    Science.gov (United States)

    Grolier, Jean-Pierre E.; del Río, Jose Manuel

    2009-01-01

    We have performed a detailed study of the thermodynamics of the titration process in an isothermal titration calorimeter with full cells. We show that the relationship between the enthalpy and the heat measured is better described in terms of the equation Δ H = Winj + Q (where Winj is the work necessary to carry out the titration) than in terms of ΔH = Q. Moreover, we show that the heat of interaction between two components is related to the partial enthalpy of interaction at infinite dilution of the titrant component, as well as to its partial volume of interaction at infinite dilution. PMID:20054472

  8. Titration Calorimetry Applied to the Thermokinetics Study of Consecutive First-order Reactions

    Institute of Scientific and Technical Information of China (English)

    SHI Jing-Yan; LI Jie; WANG Zhi-Yong; LIU Yu-Wen; WANG Cun-Xin

    2008-01-01

    The thermokinetic mathematical models for consecutive first-order reactions in titration period and the stopped-titration reaction period were proposed for titration calorimetry, based on which, thermodynamic parameters (reaction enthalpies, △rHm1 and △rHm2) and kinetic parameters (rate constants, k1 and k2) of the consecutive first-order reactions could be obtained by directly simulating the calorimetric curve from a single experiment with the method of nonlinear least squares regression (NLLS).The reliability of the model has been verified by investigating the reaction of the saponification of diethyl succinate in an aqueous ethanol solvent.

  9. Manufacturing and automation

    Directory of Open Access Journals (Sweden)

    Ernesto Córdoba Nieto

    2010-04-01

    Full Text Available The article presents concepts and definitions from different sources concerning automation. The work approaches automation by virtue of the author’s experience in manufacturing production; why and how automation prolects are embarked upon is considered. Technological reflection regarding the progressive advances or stages of automation in the production area is stressed. Coriat and Freyssenet’s thoughts about and approaches to the problem of automation and its current state are taken and examined, especially that referring to the problem’s relationship with reconciling the level of automation with the flexibility and productivity demanded by competitive, worldwide manufacturing.

  10. 混合离子的沉淀准确滴定%Precipitation Titration for Multiple Ions

    Institute of Scientific and Technical Information of China (English)

    乔成立

    2016-01-01

    The absolute value of titration break in precipitation titration is deduced with the Ringbom titration curve equation, and the conditions for accurate precipitation titration are thus deduced with the absolute value of the titration break.%用沉淀滴定的林邦滴定曲线方程推导滴定突跃的绝对值,用滴定突跃的绝对值推导混合离子准确滴定的条件。

  11. Potentiometric urea biosensor utilizing nanobiocomposite of chitosan-iron oxide magnetic nanoparticles

    International Nuclear Information System (INIS)

    The iron oxide (Fe3O4) magnetic nanoparticles have been fabricated through a simple, cheap and reproducible approach. Scanning electron microscope, x-rays powder diffraction of the fabricated nanoparticles. Furthermore, the fabrication of potentiometric urea biosensor is carried out through drop casting the initially prepared isopropanol and chitosan solution, containing Fe3O4 nanoparticles, on the glass fiber filter with a diameter of 2 cm and a copper wire (of thickness −500 μm) has been utilized to extract the voltage signal from the functionalized nanoparticles. The functionalization of surface of the Fe3O4 nanoparticles is obtained by the electrostatically immobilization of urease onto the nanobiocomposite of the chitosan- Fe3O4 in order to enhance the sensitivity, specificity, stability and reusability of urea biosensor. Electrochemical detection procedure has been adopted to measure the potentiometric response over the wide logarithmic concentration range of the 0.1 mM to 80 mM. The Fe3O4 nanoparticles based urea biosensor depicts good sensitivity with ∼42 mV per decade at room temperature. Durability of the biosensor could be considerably enhanced by applying a thin layer of the nafion. In addition, the reasonably stable output response of the biosensor has been found to be around 12 sec.

  12. Potentiometric urea biosensor based on multi-walled carbon nanotubes (MWCNTs)/silica composite material

    International Nuclear Information System (INIS)

    A novel potentiometric urea biosensor has been fabricated with urease (Urs) immobilized multi-walled carbon nanotubes (MWCNTs) embedded in silica matrix deposited on the surface of indium tin oxide (ITO) coated glass plate. The enzyme Urs was covalently linked with the exposed free -COOH groups of functionalized MWCNTs (F-MWCNTs), which are subsequently incorporated within the silica matrix by sol-gel method. The Urs/MWCNTs/SiO2/ITO composite modified electrode was characterized by Fourier transform infrared (FTIR) spectroscopy, thermal gravimetric analysis (TGA) and UV-visible spectroscopy. The morphologies and electrochemical performance of the modified Urs/MWCNTs/SiO2/ITO electrode have been investigated by scanning electron microscopy (SEM) and potentiometric method, respectively. The synergistic effect of silica matrix, F-MWCNTs and biocompatibility of Urs/MWCNTs/SiO2 made the biosensor to have the excellent electro catalytic activity and high stability. The resulting biosensor exhibits a good response performance to urea detection with a wide linear range from 2.18 x 10-5 to 1.07 x 10-3 M urea. The biosensor shows a short response time of 10-25 s and a high sensitivity of 23 mV/decade/cm2.

  13. Potentiometric urea biosensor based on multi-walled carbon nanotubes (MWCNTs)/silica composite material

    Energy Technology Data Exchange (ETDEWEB)

    Ahuja, Tarushee [National Physical Laboratory (Council of Scientific and Industrial Research), Dr. K.S. Krishnan Road, New Delhi-110012 (India); Department of Applied Chemistry, Delhi College of Engineering, University of Delhi, Bawana Road, Delhi-110042 (India); Kumar, D. [Department of Applied Chemistry, Delhi College of Engineering, University of Delhi, Bawana Road, Delhi-110042 (India); Singh, Nahar; Biradar, A.M. [National Physical Laboratory (Council of Scientific and Industrial Research), Dr. K.S. Krishnan Road, New Delhi-110012 (India); Rajesh, E-mail: rajesh_csir@yahoo.com [National Physical Laboratory (Council of Scientific and Industrial Research), Dr. K.S. Krishnan Road, New Delhi-110012 (India)

    2011-03-12

    A novel potentiometric urea biosensor has been fabricated with urease (Urs) immobilized multi-walled carbon nanotubes (MWCNTs) embedded in silica matrix deposited on the surface of indium tin oxide (ITO) coated glass plate. The enzyme Urs was covalently linked with the exposed free -COOH groups of functionalized MWCNTs (F-MWCNTs), which are subsequently incorporated within the silica matrix by sol-gel method. The Urs/MWCNTs/SiO{sub 2}/ITO composite modified electrode was characterized by Fourier transform infrared (FTIR) spectroscopy, thermal gravimetric analysis (TGA) and UV-visible spectroscopy. The morphologies and electrochemical performance of the modified Urs/MWCNTs/SiO{sub 2}/ITO electrode have been investigated by scanning electron microscopy (SEM) and potentiometric method, respectively. The synergistic effect of silica matrix, F-MWCNTs and biocompatibility of Urs/MWCNTs/SiO{sub 2} made the biosensor to have the excellent electro catalytic activity and high stability. The resulting biosensor exhibits a good response performance to urea detection with a wide linear range from 2.18 x 10{sup -5} to 1.07 x 10{sup -3} M urea. The biosensor shows a short response time of 10-25 s and a high sensitivity of 23 mV/decade/cm{sup 2}.

  14. Correlation between Electrical Properties and Potentiometric Response of CS-Clay Nanocomposite Membranes

    Directory of Open Access Journals (Sweden)

    M. Oviedo Mendoza

    2015-01-01

    Full Text Available The aim of this work is to study the relationship between electrical, structure, and potentiometric response to nitrate anions using Ion Selective Electrodes (ISE. These ISE are based on chitosan-montmorillonite nanocomposite membranes with different content of montmorillonite. Membrane properties have been studied using SEM, FTIR, and impedance spectroscopy measurements. With the advent of impedance spectroscopy one is allowed to obtain the DC conductivity dependence on montmorillonite concentration and the percolation threshold. Additionally, the potentiometric response to nitrate anions of ISE based on chitosan-clay nanocomposite has been investigated. It is shown that the properties and performance of these membrane electrodes depend upon the clay wt% and that the best sensitivity to nitrate ions (with detection limit 7 × 10−5 M is obtained near the percolation concentration ca. 8 ± 2.5 wt% of clay. This observation is traceable to higher clay content (higher agglomeration that tends to decrease the intercalation and absorption of the number of chitosan chains in the interlayer space of montmorillonite.

  15. Potentiometric Multisensory Systems with Novel Ion-Exchange Polymer-Based Sensors for Analysis of Drugs

    Directory of Open Access Journals (Sweden)

    Olga V. Bobreshova

    2012-01-01

    Full Text Available This paper examines potentiometric multisensory systems that consist of novel cross-sensitive PD-sensors (Potential Donnan-sensors. The analytical signal of PD-sensors is the Donnan potential at the ion-exchange polymer/electrolyte test solution interface. The use of novel sensors for the quantitative analysis of multicomponent aqueous solutions of amino acids, vitamins and medical substances is based on protolytic and ion-exchange reactions at the interfaces of ion-exchangers and test solutions. The potentiometric sensor arrays consist of PD-sensors and ion-selective electrodes. Such systems were developed for the multicomponent quantitative analysis of lysine monohydrochloride, thiamine chloride and novocaine hydrochloride solutions that contained salts of alkaline and alkaline-earth metals, as well as for mixed solutions of nicotinic acid and pyridoxine hydrochloride. Multivariate methods of analysis were used for sensor calibration and the analysis of the total response of sensor arrays. The errors of measurement of the electrolytes in aqueous solutions did not exceed 10%. The developed multisensory systems were used to determine the composition of a therapeutic “Mineral salt with low content of sodium chloride” and to determine concentrations of novocaine in sewage samples from a dental clinic.

  16. Array of potentiometric sensors for simultaneous determination of copper, silver, and cadmium ions in complex mixtures

    International Nuclear Information System (INIS)

    Graphical abstract: - Abstract: A programmed switching system combined with an array of potentiometric sensors consisting of seven potentiometric sensors (i.e., ion-selective or cross-selective electrodes) was connected directly to a pH/potentiometer and a computer (PC) to sequentially acquire the potential corresponding to water sample mixtures. The acquired potentials were recorded and saved on the PC and were used as input variables for an artificial neural network to simultaneously yield the concentrations of Cd2+, Cu2+, and Ag+ in simple and complex mixtures. A feed-forward, back propagation network with a Levenburg–Maquart algorithm was employed to optimize the network parameters. Certain characteristics of each of the seven ion-selective electrodes, including selectivity coefficients, calibration curves, and response times, were also studied. A five-second delay time was used when recording the potentials of the electrodes using the switching system. The array system was also optimized for the selection of the ion-selective electrodes. A four-electrode array system was found to be the best choice for the prediction of Cd2+, Ag+ and Cu2+ ion concentration, but application of all seven ion-selective electrodes was necessary for prediction of these primary ions in samples containing a combination of zinc and nickel ions as interfering ions.

  17. New molecularly-imprinted polymer for carnitine and its application as ionophore in potentiometric selective membranes.

    Science.gov (United States)

    Moret, Joséphine; Moreira, Felismina T C; Almeida, Sofia A A; Sales, M Goreti F

    2014-10-01

    Carnitine (CRT) is a biological metabolite found in urine that contributes in assessingseveral disease conditions, including cancer. Novel quick screening procedures for CRT are therefore fundamental. This work proposes a novel potentiometric device where molecularly imprinted polymers (MIPs) were used as ionophores. The host-tailored sites were imprinted on a polymeric network assembled by radical polymerization of methacrylic acid (MAA) and trimethylpropane trimethacrylate (TRIM). Non-imprinted polymers (NIPs) were produced as control by removing the template from the reaction media. The selective membrane was prepared by dispersing MIP or NIP particles in plasticizer and poly(vinyl chloride), PVC, and casting this mixture over a solid contact support made of graphite. The composition of the selective membrane was investigated with regard to kind/amount of sensory material (MIP or NIP), and the need for a lipophilic additive. Overall, MIP sensors with additive exhibited the best performance, with near-Nernstian response down to ~1×10(-4)mol L(-1), at pH5, and a detection limit of ~8×10(-5)mol L(-1). Suitable selectivity was found for all membranes, assessed by the matched potential method against some of the most common species in urine (urea, sodium, creatinine, sulfate, fructose and hemoglobin). CRT selective membranes including MIP materials were applied successfully to the potentiometric determination of CRT in urine samples. PMID:25175239

  18. An automated swimming respirometer

    DEFF Research Database (Denmark)

    STEFFENSEN, JF; JOHANSEN, K; BUSHNELL, PG

    1984-01-01

    An automated respirometer is described that can be used for computerized respirometry of trout and sharks.......An automated respirometer is described that can be used for computerized respirometry of trout and sharks....

  19. Configuration Management Automation (CMA)

    Data.gov (United States)

    Department of Transportation — Configuration Management Automation (CMA) will provide an automated, integrated enterprise solution to support CM of FAA NAS and Non-NAS assets and investments. CMA...

  20. Application of Ion-Association Titration for the Assay of Cyproheptadine Hydrochloride in Pharmaceuticals

    OpenAIRE

    kanakapura Basavaiah; Raghu, Madihalli S.

    2012-01-01

    Two simple and rapid titrimetric methods are described for the determination of cyproheptadine hydrochloride (CPH) in pharmaceuticals. The proposed methods are based on the solvent extraction-titration of CPH with two ion association reagents, sodium lauryl sulphate (SLS), (method A), and tetraphenylborate (TPB), (method B). In method A, SLS was used as titrant and the titration was carried out in the presence of dilute sulphuric acid and chloroform using dimethyl yellow as indicator, whereas...

  1. Opuntia ficus indica (L.) Fruit Extract as Natural Indicator in Acid-Base Titration

    OpenAIRE

    Manoj A. Suva

    2014-01-01

    In routine experiments synthetic indicators are the choice of acid base titrations. But there are some limitations like environmental pollution, availability and higher cost which leads to search for natural compounds as an acid base indicator was started. The present work highlights theexploit of the methanolic and aqueous extract of the fruit of Opuntia ficus indica plants as a natural acid base indicator in acid base titrations. Opuntia ficus indica plant was identified and fruits were was...

  2. Report of a patient chewing fentanyl patches who was titrated onto methadone

    OpenAIRE

    Dale, Eric; Ashby, Fleur; Seelam, Kalyan

    2009-01-01

    This case report discusses the clinical presentation and management of a patient presenting to substance misuse services reporting chewing fentanyl patches in addition to wearing them transdermally. The patient was successfully titrated onto methadone 30 mg. Only one previously reported case of an individual chewing fentanyl patches was found in the literature; no case reports were found where treatment involved titrating the patient onto methadone. The pharmacology and illicit use of fentany...

  3. Complexometric titration with potenciometric indicator to determination of calcium and magnesium in soil extracts¹

    OpenAIRE

    Claudia Mara Pereira; Cristhiane Anete Neiverth; Shizuo Maeda; Marcela Guiotoku; Luziane Franciscon

    2011-01-01

    This study proposes a method of direct and simultaneous determination of the amount of Ca2+ and Mg2+ present in soil extracts using a Calcium Ion-Selective Electrode and by Complexometric Titration (ISE-CT). The results were compared to those obtained by conventional analytical techniques of Complexometric Titration (CT) and Flame Atomic Absorption Spectrometry (FAAS). There were no significant differences in the determination of Ca2+ and Mg2+ in comparison with CT and FAAS, at a 95 % confide...

  4. A coulometric Gran titration method for the determination of strong and weak acids in freshwater

    OpenAIRE

    Røgeberg, E.

    1987-01-01

    A modefied Gran titration procedure for the determination of strong and weak acids in freshwater is described. The titrations are carried out by coulometric generation of hydroxide ions in the pH range 3.6-10.3. The method measures the amount of non-volatile strong and weak acids with a precision of + - 5 moles/l. Application to natural water samples is demonstrated.

  5. Detection of Neutralising Antibody Titration in Vaccinated Owned and Stray Dogs against Rabies Virus

    OpenAIRE

    GAZİ, Aliye Ebru; AK, Seyyal

    2011-01-01

    The aim of this study was to determine the titers of neutralising antibodies against rabies virus in five hundred vaccinated owned and stray dogs within the Istanbul province. The levels of the neutralising antibody titration in the blood serum were evaluated by Enzyme-Linked Immunosorbent Assay (ELISA) method. Sixty five (13%) of the dogs examined had adequate level (0.5 IU/ml and over) of antibody titration. Also, the effects on the formation of the neutralising antibody levels following th...

  6. Appropriate conditions for polyelectrolyte titration to determine the charge of cellulosic fibers

    OpenAIRE

    Horvath, Elisabet

    2003-01-01

    The polyelectrolyte titration method has been developed overthe years in order to determine the surface charge ofcellulosic fibers. The conditions have been varied depending onthe author. This work has been aimed at resolving theappropriate conditions for measuring the charge, such aselectrolyte concentration and molecular mass of thepolyelectrolyte. The charge ratio of variously treated pulpswas also investigated. The polyelectrolyte titration technique is based on a 1:1adsorption stoichiome...

  7. APPLICATION OF ION-ASSOCIATION TITRATION FOR THE ASSAY OF BUPROPION HYDROCHLORIDE IN PHARMACEUTICALS

    OpenAIRE

    Abdulrahman, Sameer A. M.; Kanakapura Basavaiah

    2011-01-01

    Two simple and rapid titrimetric methods are described for the determination of bupropion hydrochloride (BUPH) in pharmaceuticals. The proposed methods are based on the solvent extraction-titration of BUPH with two ion-association reagents, i.e., sodium lauryl sulphate (SLS) and tetraphenylborate (TPB). In method A, SLS was used as titrant and the titration was carried out in the presence of dilute sulphuric acid and chloroform using dimethyl yellow as indicator whereas in method B, the titr...

  8. Determination of the aggregation number for micelles by isothermal titration calorimetry

    DEFF Research Database (Denmark)

    Olesen, Niels Erik; Holm, Rene; Westh, Peter

    2014-01-01

    Isothermal titration calorimetry (ITC) has previously been applied to estimate the aggregation number (n), Gibbs free energy (ΔG), enthalpy (ΔH) and entropy (ΔS) of micellization. However, some difficulties of micelle characterization by ITC still remain; most micelles have aggregation numbers...... insight into optimal design of titration protocols for micelle characterization. By applying the new method, the aggregation number of sodium dodecyl sulphate and glycochenodeoxycholate was determined at concentrations around their critical micelle concentration (CMC)...

  9. Measuring the sequence-affinity landscape of antibodies with massively parallel titration curves

    OpenAIRE

    Adams, Rhys M.; Kinney, Justin B.; Mora, Thierry; Walczak, Aleksandra M.

    2016-01-01

    Despite the central role that antibodies play in the adaptive immune system and in biotechnology, much remains unknown about the quantitative relationship between an antibody's amino acid sequence and its antigen binding affinity. Here we describe a new experimental approach, called Tite-Seq, that is capable of measuring binding titration curves and corresponding affinities for thousands of variant antibodies in parallel. The measurement of titration curves eliminates the confounding effects ...

  10. A practical protocol for titrating "optimal" PEEP in acute lung injury: recruitment maneuver and PEEP decrement.

    OpenAIRE

    Suh, Gee Young; Kwon, O Jung; Yoon, Jong Wook; Park, Sang Joon; Ham, Hyoung Suk; Kang, Soo Jung; Koh, Won-Jung; Chung, Man Pyo; Kim, Ho Joong

    2003-01-01

    This study was conducted to evaluate the effectiveness and safety of a practical protocol for titrating positive end-expiratory pressure (PEEP) involving recruitment maneuver (RM) and decremental PEEP. Seventeen consecutive patients with acute lung injury who underwent PEEP titration were included in the analysis. After baseline ventilation, RM (continuous positive airway pressure, 35 cm H2O for 45 sec) was performed and PEEP was increased to 20 cmH2O or the highest PEEP guaranteeing the mini...

  11. Workflow automation architecture standard

    Energy Technology Data Exchange (ETDEWEB)

    Moshofsky, R.P.; Rohen, W.T. [Boeing Computer Services Co., Richland, WA (United States)

    1994-11-14

    This document presents an architectural standard for application of workflow automation technology. The standard includes a functional architecture, process for developing an automated workflow system for a work group, functional and collateral specifications for workflow automation, and results of a proof of concept prototype.

  12. Determination of free acid in U(VI)-Al(III) solution by Gran plot titration

    International Nuclear Information System (INIS)

    The determination method of free acid in spent U-Al nuclear fuel solutions by Gran plot titration was described. Effect of U(VI) and Al(III) on the alkalimetric titration of nitric acid was investigation in oxalate complexing media as well as in noncomplexing media. Positive biases were observed in both titration media when the end-point was estimated by the Gran plot method. It was found that the cause of the bias was U(VI) in the oxalate complexing media, but Al(III) in the noncomplexing media. The relative error was less than 1% in the titration of 0.1 M HNO3 at a U(VI):Al(III):H+ mole ratio of up to 2:12:1 as long as the pH of the oxalate titration media was sustained to be below 5.0 at the beginning of titration. The method was successfully applied to the determination of nitric acid in a solution of HANARO reactor fuel with U:Al mole ratio of 1:6

  13. Titration of strong and weak acids by sequential injection analysis technique.

    Science.gov (United States)

    Maskula, S; Nyman, J; Ivaska, A

    2000-05-31

    A sequential injection analysis (SIA) titration method has been developed for acid-base titrations. Strong and weak acids in different concentration ranges have been titrated with a strong base. The method is based on sequential aspiration of an acidic sample zone and only one zone of the base into a carrier stream of distilled water. On their way to the detector, the sample and the reagent zones are partially mixed due to the dispersion and thereby the base is partially neutralised by the acid. The base zone contains the indicator. An LED-spectrophotometer is used as detector. It senses the colour of the unneutralised base and the signal is recorded as a typical SIA peak. The peak area of the unreacted base was found to be proportional to the logarithm of the acid concentration. Calibration curves with good linearity were obtained for a strong acid in the concentration ranges of 10(-4)-10(-2) and 0.1-3 M. Automatic sample dilution was implemented when sulphuric acid at concentration of 6-13 M was titrated. For a weak acid, i.e. acetic acid, a linear calibration curve was obtained in the range of 3x10(-4)-8x10(-2) M. By changing the volumes of the injected sample and the reagent, different acids as well as different concentration ranges of the acids can be titrated without any other adjustments in the SIA manifold or the titration protocol. PMID:18967966

  14. Shoe-String Automation

    Energy Technology Data Exchange (ETDEWEB)

    Duncan, M.L.

    2001-07-30

    Faced with a downsizing organization, serious budget reductions and retirement of key metrology personnel, maintaining capabilities to provide necessary services to our customers was becoming increasingly difficult. It appeared that the only solution was to automate some of our more personnel-intensive processes; however, it was crucial that the most personnel-intensive candidate process be automated, at the lowest price possible and with the lowest risk of failure. This discussion relates factors in the selection of the Standard Leak Calibration System for automation, the methods of automation used to provide the lowest-cost solution and the benefits realized as a result of the automation.

  15. Effect of temperature on the protonation of N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetic acid in aqueous solutions: Potentiometric and calorimetric studies

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xingliang [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Chemical Sciences Div.; China Academy of Engineering Physics, Mianyang (China). Inst. of Nuclear Physics and Chemistry; Zhang, Zhicheng [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Chemical Sciences Div.; Endrizzi, Francesco [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Chemical Sciences Div.; Martin, Leigh R. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Luo, Shunzhong [China Academy of Engineering Physics, Mianyang (China). Inst. of Nuclear Physics and Chemistry; Rao, Linfeng [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Chemical Sciences Div.

    2015-06-01

    The TALSPEAK process (Trivalent Actinide Lanthanide Separations by Phosphorus-reagent Extraction from Aqueous Komplexes) has been demonstrated in several pilot-scale operations to be effective at separating trivalent actinides (An3+) from trivalent lanthanides (Ln3+). However, fundamental studies have revealed undesired aspects of TALSPEAK, such as the significant partitioning of Na+, lactic acid, and water into the organic phase, thermodynamically unpredictable pH dependence, and the slow extraction kinetics. In the modified TALSPEAK process, the combination of the aqueous holdback complexant HEDTA (N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetic acid) with the extractant HEH[EHP] (2-ethyl(hexyl) phosphonic acid mono-2-ethylhexyl ester) in the organic phase has been found to exhibit a nearly flat pH dependence between 2.5 and 4.5 and more rapid phase transfer kinetics for the heavier lanthanides. To help understand the speciation of Ln3+ and An3+ in the modified TALSPEAK, systematic studies are underway on the thermodynamics of major reactions in the HEDTA system under conditions relevant to the process (e.g., higher temperatures). Thermodynamics of the protonation and complexation of HEDTA with Ln3+ were studied at variable temperatures. Equilibrium constants and enthalpies were determined by a combination of techniques including potentiometry and calorimetry. This paper presents the protonation constants of HEDTA at T = (25 to 70) °C. The potentiometric titrations have demonstrated that, stepwise, the first two protonation constants decrease and the third one slightly increases with the increase of temperature. This trend is in good agreement with the enthalpy of protonation directly determined by calorimetry. The results of NMR analysis further confirm that the first two protonation reactions occur on the diamine nitrogen atoms, while the third protonation reaction occurs on the

  16. Development of automated analytical system using robots. Development of automated spectrophotometer

    International Nuclear Information System (INIS)

    An automated analytical system for the measurement of U and Pu concentrations, acidity and radioactivity has been developed since 1993 at the Tokai Reprocessing Plant. The total system is composed of three units, the unit of spectrophotometry, that of titration and that of radioactivity counting. Each unit consists of a robot, an analytical instrument and a computer. The robot operates pretreatment of the samples and to set them into the analytical instrument. The personal computer is used to control the robot and the analytical instrument, and also send the measurement results to the host computer. This report describes the present status of the development of the system and the results of the basic test for the spectrophotometry unit. (author)

  17. Potentiometric Electronic Tongue to Resolve Mixtures of Sulfide and Perchlorate Anions

    Directory of Open Access Journals (Sweden)

    Deivy Wilson

    2011-03-01

    Full Text Available This work describes the use of an array of potentiometric sensors and an artificial neural network response model to determine perchlorate and sulfide ions in polluted waters, by what is known as an electronic tongue. Sensors used have been all-solid-state PVC membrane selective electrodes, where their ionophores were different metal-phtalocyanine complexes with specific and anion generic responses. The study case illustrates the potential use of electronic tongues in the quantification of mixtures when interfering effects need to be counterbalanced: relative errors in determination of individual ions can be decreased typically from 25% to less than 5%, if compared to the use of a single proposed ion-selective electrode.

  18. Highly efficient potentiometric glucose biosensor based on functionalized InN quantum dots

    Science.gov (United States)

    Alvi, N. H.; Soto Rodriguez, P. E. D.; Gómez, V. J.; Kumar, Praveen; Amin, G.; Nur, O.; Willander, M.; Nötzel, R.

    2012-10-01

    We present a fast, highly sensitive, and efficient potentiometric glucose biosensor based on functionalized InN quantum-dots (QDs). The InN QDs are grown by molecular beam epitaxy. The InN QDs are bio-chemically functionalized through physical adsorption of glucose oxidase (GOD). GOD enzyme-coated InN QDs based biosensor exhibits excellent linear glucose concentration dependent electrochemical response against an Ag/AgCl reference electrode over a wide logarithmic glucose concentration range (1 × 10-5 M to 1 × 10-2 M) with a high sensitivity of 80 mV/decade. It exhibits a fast response time of less than 2 s with good stability and reusability and shows negligible response to common interferents such as ascorbic acid and uric acid. The fabricated biosensor has full potential to be an attractive candidate for blood sugar concentration detection in clinical diagnoses.

  19. Potentiometric studies on mixed-ligand chelates of uranyl ion with carboxylic acid phenolic acids

    International Nuclear Information System (INIS)

    Mixed ligand complexes of UO22+ with bidentate carboxylic and phenolic acids have been studied potentiometrically at 30 ± 0.1degC and μ=0.2M (NaClO4). 1:1 and 1:2 complexes of UO22+ with phthalic acid (PTHA), maleic acid (MAE), malonic acid (MAL), quinolinic acid (QA), 5-sulphosalicylic acid (5-SSA), salicylic acid (SA), and only 1:1 complexes in the case of mandelic acid (MAD) have been detected. The formation of 1:1:1 mixed ligand complexes has been inferred from simultaneous equilibria in the present study. The values of ΔlogK, Ksub(DAL), Ksub(2LA) or Ksub(2AL) for the ternary complexes have been calculated. The stabilities of mixed ligand complexes depend on the size of the chelate ring and the stabilities of the binary complexes. (author). 15 refs

  20. Open ISEmeter: An open hardware high-impedance interface for potentiometric detection.

    Science.gov (United States)

    Salvador, C; Mesa, M S; Durán, E; Alvarez, J L; Carbajo, J; Mozo, J D

    2016-05-01

    In this work, a new open hardware interface based on Arduino to read electromotive force (emf) from potentiometric detectors is presented. The interface has been fully designed with the open code philosophy and all documentation will be accessible on web. The paper describes a comprehensive project including the electronic design, the firmware loaded on Arduino, and the Java-coded graphical user interface to load data in a computer (PC or Mac) for processing. The prototype was tested by measuring the calibration curve of a detector. As detection element, an active poly(vinyl chloride)-based membrane was used, doped with cetyltrimethylammonium dodecylsulphate (CTA(+)-DS(-)). The experimental measures of emf indicate Nernstian behaviour with the CTA(+) content of test solutions, as it was described in the literature, proving the validity of the developed prototype. A comparative analysis of performance was made by using the same chemical detector but changing the measurement instrumentation. PMID:27250474

  1. Potentiometric stripping analysis of lead and cadmium leaching from dental prosthetic materials and teeth

    Directory of Open Access Journals (Sweden)

    GORAN M. NIKOLIC

    2004-07-01

    Full Text Available Potentiometric stipping analysis (PSA was applied for the determination of lead and cadmium leaching from dental prosthetic materials and teeth. The soluble lead content in finished dental implants was found to be much lower than that of the individual components used for their preparation. Cadmium was not detected in dental implants and materials under the defined conditions. The soluble lead and cadmium content of teeth was slightly lower than the lead and cadmium content in whole teeth (w/w reported by other researchers, except in the case of a tooth with removed amalgam filling. The results of this work suggest that PSA may be a good method for lead and cadmium leaching studies for investigation of the biocompatibility of dental prosthetic materials.

  2. Gas-potentiometric method with solid electrolyte oxygen sensors for the investigation of combustion.

    Science.gov (United States)

    Lorenz, H; Tittmann, K; Sitzki, L; Trippler, S; Rau, H

    1996-09-01

    Gas-potentiometric analysis using oxide-ion-conducting solid electrolytes as stabilized zirconia is a worthwhile method for the investigation of combustion processes. In the case of gas and oil flames specific parameters like the flame contour, the degree of burn-out and mixing can be determined and information about flame turbulence and reaction density can be gained from the temporal resolution of the sensor signal. Measurements carried out with solid electrolyte oxygen sensors in a fluidized bed show that combustion processes of solid fuels are also analyzable. This analysis results in fuel specific burn-out curves finally leading to burn-out times and to parameters of a macrokinetics of the combustion process as well as to ideas about the burn-out mechanism. From the resulting constants of the effective reaction rate a reactivity relative to bituminous coal coke can be given for any solid fuel. PMID:15048356

  3. Lanthanide recognition: A Ho3+ potentiometric membrane sensor as a probe for determination of terazosin

    International Nuclear Information System (INIS)

    In this study, complexation of N'-(1-pyridin-2-ylmethylene)-2-furohydrazide (NFH) with some metal ions was investigated by conductometry and spectroscopy. Then, a Ho3+ potentiometric membrane sensor was prepared based on the highly selective complexation between this ionophore and Ho3+. These new ionophores are more selective than the previously reported ones. In this work, for the first time, the proposed sensor was applied in indirect determination of the terazocine in its pharmaceutical formulation. The interest in constructing lanthanide sensors arises because they have similar ionic radii to calcium, but a higher charge density, which allows them to be used as probes to find the interactions between Ca2+ and biologically important molecules.

  4. Bio-assisted potentiometric multisensor system for purity evaluation of recombinant protein A.

    Science.gov (United States)

    Voitechovič, Edita; Korepanov, Anton; Kirsanov, Dmitry; Jahatspanian, Igor; Legin, Andrey

    2016-08-15

    Recombinant proteins became essential components of drug manufacturing. Quality control of such proteins is routine task, which usually requires a lot of time, expensive reagents, specialized equipment and highly educated personnel. In this study we propose a new concept for protein purity evaluation that is based on application of bio-assisted potentiometric multisensor system. The model object for analysis was recombinant protein A from Staphylococcus aureus (SpA), which is commonly used for monoclonal antibody purification. SpA solutions with different amount of host cell related impurities (Escherichia coli, bacterial lysate) were analyzed. Two different bio-transducers were employed: proteinase K from Tritirachium album and baker's yeast Saccharomyces cerevisiae. It was shown that both bio-transducers are able to induce changes in pure and lysate-contaminated SpA samples. Different products of yeast digestion and proteolysis with proteinase of pure SpA and lysate were detected with size exclusion high-performance liquid chromatography (SE-HPLC). The induced changes of chemical composition are detectible with potentiometric multisensor system and can be related to SpA purity through projection on latent structures (PLS) regression technique. The proposed method allows for estimation of the impurity content with 12% accuracy using proteinase K and 16% accuracy using baker's yeast. The suggested approach could be useful for early contamination warning at initial protein purification steps. The analysis requires no expensive materials and equipment, no bio-material immobilization, and its duration time is comparable with other commonly used methods like chromatography or electrophoresis though the main part of this time is related to the sample preparation. PMID:27260439

  5. Potentiometric Urea Biosensor Based on an Immobilised Fullerene-Urease Bio-Conjugate

    Directory of Open Access Journals (Sweden)

    Kasra Saeedfar

    2013-12-01

    Full Text Available A novel method for the rapid modification of fullerene for subsequent enzyme attachment to create a potentiometric biosensor is presented. Urease was immobilized onto the modified fullerene nanomaterial. The modified fullerene-immobilized urease (C60-urease bioconjugate has been confirmed to catalyze the hydrolysis of urea in solution. The biomaterial was then deposited on a screen-printed electrode containing a non-plasticized poly(n-butyl acrylate (PnBA membrane entrapped with a hydrogen ionophore. This pH-selective membrane is intended to function as a potentiometric urea biosensor with the deposition of C60-urease on the PnBA membrane. Various parameters for fullerene modification and urease immobilization were investigated. The optimal pH and concentration of the phosphate buffer for the urea biosensor were 7.0 and 0.5 mM, respectively. The linear response range of the biosensor was from 2.31 × 10−3 M to 8.28 × 10−5 M. The biosensor’s sensitivity was 59.67 ± 0.91 mV/decade, which is close to the theoretical value. Common cations such as Na+, K+, Ca2+, Mg2+ and NH4+ showed no obvious interference with the urea biosensor’s response. The use of a fullerene-urease bio-conjugate and an acrylic membrane with good adhesion prevented the leaching of urease enzyme and thus increased the stability of the urea biosensor for up to 140 days.

  6. Real-Time Telemetry System for Amperometric and Potentiometric Electrochemical Sensors

    Directory of Open Access Journals (Sweden)

    Ching-Hsing Luo

    2011-09-01

    Full Text Available A real-time telemetry system, which consists of readout circuits, an analog-to-digital converter (ADC, a microcontroller unit (MCU, a graphical user interface (GUI, and a radio frequency (RF transceiver, is proposed for amperometric and potentiometric electrochemical sensors. By integrating the proposed system with the electrochemical sensors, analyte detection can be conveniently performed. The data is displayed in real-time on a GUI and optionally uploaded to a database via the Internet, allowing it to be accessed remotely. An MCU was implemented using a field programmable gate array (FPGA to filter noise, transmit data, and provide control over peripheral devices to reduce power consumption, which in sleep mode is 70 mW lower than in operating mode. The readout circuits, which were implemented in the TSMC 0.18-μm CMOS process, include a potentiostat and an instrumentation amplifier (IA. The measurement results show that the proposed potentiostat has a detectable current range of 1 nA to 100 μA, and linearity with an R2 value of 0.99998 in each measured current range. The proposed IA has a common-mode rejection ratio (CMRR greater than 90 dB. The proposed system was integrated with a potentiometric pH sensor and an amperometric nitrite sensor for in vitro experiments. The proposed system has high linearity (an R2 value greater than 0.99 was obtained in each experiment, a small size of 5.6 cm × 8.7 cm, high portability, and high integration.

  7. Automated stopcock actuator

    OpenAIRE

    Vandehey, N. T.; O'Neil, J.P.

    2015-01-01

    Introduction We have developed a low-cost stopcock valve actuator for radiochemistry automation built using a stepper motor and an Arduino, an open-source single-board microcontroller. The con-troller hardware can be programmed to run by serial communication or via two 5–24 V digital lines for simple integration into any automation control system. This valve actuator allows for automated use of a single, disposable stopcock, providing a number of advantages over stopcock manifold systems ...

  8. The Adaptive Automation Design

    OpenAIRE

    Calefato, Caterina; Montanari, Roberto; TESAURI, Francesco

    2008-01-01

    After considering the positive effects of adaptive automation implementation, this chapter focuses on two partly overlapping phenomena: on the one hand, the role of trust in automation is considered, particularly as to the effects of overtrust and mistrust in automation's reliability; on the other hand, long-term lack of exercise on specific operation may lead users to skill deterioration. As a future work, it will be interesting and challenging to explore the conjunction of adaptive automati...

  9. Service functional test automation

    OpenAIRE

    Hillah, Lom Messan; Maesano, Ariele-Paolo; Rosa, Fabio; Maesano, Libero; Lettere, Marco; Fontanelli, Riccardo

    2015-01-01

    This paper presents the automation of the functional test of services (black-box testing) and services architectures (grey-box testing) that has been developed by the MIDAS project and is accessible on the MIDAS SaaS. In particular, the paper illustrates the solutions of tough functional test automation problems such as: (i) the configuration of the automated test execution system against large and complex services architectures, (ii) the constraint-based test input generation, (iii) the spec...

  10. Observation wells used in the creation of the generalized potentiometric surface of the Arikaree aquifer, Pine Ridge Indian Reservation and Bennett County, South Dakota

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — This data set describes observation wells completed in the Arikaree aquifer that were used to create a map of the generalized potentiometric surface of the Arikaree...

  11. Spring point coverage for the potentiometric coverages for the Inyan Kara, Minnekahta, Minnelusa, Madison, and Deadwood Aquifers in the Black Hills Area, South Dakota

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — This dataset describes springs in the Black Hills area that were used to create potentiometric surface maps for the Inyan Kara, Minnekahta, Minnelusa, Madison, and...

  12. Regional potentiometric-surface contours by Bedinger and Harrill (2004), for the Death Valley regional ground-water flow system study, Nevada and California

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — The contours in this digital data set represent the regional potentiometric surface developed by Bedinger and Harrill (2004) to assess potential interbasin flow in...

  13. Estimated potentiometric surface by D'Agnese and others (1998), for the Death Valley regional ground-water flow system study, Nevada and California

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — D'Agnese and others (1998) developed a potentiometric surface to conceptualize the regional ground-water flow system and to construct numerical flow models of the...

  14. Automated Weather Observing System

    Data.gov (United States)

    Department of Transportation — The Automated Weather Observing System (AWOS) is a suite of sensors, which measure, collect, and disseminate weather data to help meteorologists, pilots, and flight...

  15. Laboratory Automation and Middleware.

    Science.gov (United States)

    Riben, Michael

    2015-06-01

    The practice of surgical pathology is under constant pressure to deliver the highest quality of service, reduce errors, increase throughput, and decrease turnaround time while at the same time dealing with an aging workforce, increasing financial constraints, and economic uncertainty. Although not able to implement total laboratory automation, great progress continues to be made in workstation automation in all areas of the pathology laboratory. This report highlights the benefits and challenges of pathology automation, reviews middleware and its use to facilitate automation, and reviews the progress so far in the anatomic pathology laboratory. PMID:26065792

  16. Automated cloning methods.; TOPICAL

    International Nuclear Information System (INIS)

    Argonne has developed a series of automated protocols to generate bacterial expression clones by using a robotic system designed to be used in procedures associated with molecular biology. The system provides plate storage, temperature control from 4 to 37 C at various locations, and Biomek and Multimek pipetting stations. The automated system consists of a robot that transports sources from the active station on the automation system. Protocols for the automated generation of bacterial expression clones can be grouped into three categories (Figure 1). Fragment generation protocols are initiated on day one of the expression cloning procedure and encompass those protocols involved in generating purified coding region (PCR)

  17. Solubility increase of colloidal zinc hydroxide as revealed by isothermal titration calorimetry

    International Nuclear Information System (INIS)

    Highlights: • Association between zinc (II) and dipicolylamine was studied by ITC. • Increasing heat release was observed as the titration proceeded. • Thermodynamics of the association was discussed. • The increasing heat release was ascribed to solubility increase of colloidal Zn(OH)2. - Abstract: In this study, association between zinc (II) and dipicolylamine was studied by isothermal titration calorimetry. At neutral of weakly alkaline conditions, with zinc (II) in cell and dipicolylamine in syringe, increasing heat release was observed as the titration proceeded. Considering the equilibrium between Zn2+ and Zn(OH)2 at these conditions, the increasing heat release is ascribed to the increasing solubilization of colloidal Zn(OH)2 followed by neutralization of OH- by the buffer. Though quantitative determination of the increase in solubility is not accomplished, to the best of our knowledge, this is the first report about solubility increase of colloidal zinc hydroxide using calorimetric method

  18. Thermometric titration of thorium with EDTA in the presence of large excess of neutral sodium salts

    International Nuclear Information System (INIS)

    The thermometric titration of Th(IV) in the presence of neutral sodium salts, sulphuric acid or acetic acid with EDT has been studied. The effect of each on the observed heat values for the titration is discussed. For sodium perchlorate media, ΔH values of -9 and -21 kJ/mole have been estimated for the formation of the Th(IV)-EDTA chelate at μ → 0 and μ = 0.5 (NaClO4), respectively. The -ΔH values increase steadily with increase in concentration of sodium perchlorate up to at least 3M. For the titration of Th(IV) in the presence of a large excess of sodium nitrate the use of sodium iodide as a masking reagent has been examined: large amounts of Bi and Cu(II) are masked and a masking effect is observed for small amounts of Ni. (author)

  19. Purity of potassium hydrogen phthalate, determination with precision coulometric and volumetric titration--a comparison.

    Science.gov (United States)

    Recknagel, Sebastian; Breitenbach, Martin; Pautz, Joachim; Lück, Detlef

    2007-09-19

    The mass fraction of potassium hydrogen phthalate (KHP) from a specific batch was certified as an acidimetric standard. Two different analytical methods on a metrological level were used to carry out certification analysis: precision constant current coulometric and volumetric titration with NaOH. It could be shown that with a commercial automatic titration system in combination with a reliable software for the end-point detection it is possible to produce equivalent results with the same accuracy in comparison to a definite method handled by a fundamental apparatus for traceable precision coulometry. Prerequisite for titrations are that a high number of single measurement are applied which are calibrated with a high precision certified reference material. PMID:17870288

  20. The role of DNA binding sites and slow unbinding kinetics in titration-based oscillators

    CERN Document Server

    Karapetyan, Sargis

    2015-01-01

    Genetic oscillators, such as circadian clocks, are constantly perturbed by molecular noise arising from the small number of molecules involved in gene regulation. One of the strongest sources of stochasticity is the binary noise that arises from the binding of a regulatory protein to a promoter in the chromosomal DNA. In this study, we focus on two minimal oscillators based on activator titration and repressor titration to understand the key parameters that are important for oscillations and for overcoming binary noise. We show that the rate of unbinding from the DNA, despite traditionally being considered a fast parameter, needs to be slow to broaden the space of oscillatory solutions. The addition of multiple, independent DNA binding sites further expands the oscillatory parameter space for the repressor-titration oscillator and lengthens the period of both oscillators. This effect is a combination of increased effective delay of the unbinding kinetics due to multiple binding sites and increased promoter ul...

  1. Opuntia ficus indica (L. Fruit Extract as Natural Indicator in Acid-Base Titration

    Directory of Open Access Journals (Sweden)

    Manoj A. Suva

    2014-03-01

    Full Text Available In routine experiments synthetic indicators are the choice of acid base titrations. But there are some limitations like environmental pollution, availability and higher cost which leads to search for natural compounds as an acid base indicator was started. The present work highlights theexploit of the methanolic and aqueous extract of the fruit of Opuntia ficus indica plants as a natural acid base indicator in acid base titrations. Opuntia ficus indica plant was identified and fruits were washed and cleaned by distilled water, grinded by a mechanical blender and soaked in 50ml methanol for 48 hours and then triturated in mortal and pestle and the resulting solution were filtered through muslin cloth. The resulted methanolic extract and aqueous extract which was prepared by heating fruits in water for half an hour and filtered used as natural indicator foracidimetry and alkalimetry. For each type of acid base titrations t-value and standard deviation were calculated from results obtained. Natural indicator is easy to prepare, easily available and have no toxic effects and promising results were obtained when it was tested against standard synthetic indicators. Titration shows sharp colour change at the equivalence point. The equivalence points (end points obtained by the fruit extract correlate with the equivalence points obtained by standard indicators. In strong acid and strong base titration, the results obtained in the fruit's extract matched with the results obtained by standard indicator. Hence, natural indicator is found to be a very useful, readily available, nonhazardous, economical, simple to prepare and accurate for the acid-base titrations.

  2. Comparison of Titration ICP and XRF Spectrometry Methods in Determination of Cerium in Lens Polishing Powder

    International Nuclear Information System (INIS)

    Three analytical methods in determination of cerium in cerium oxide separated from monazite ore for producing lens polishing powder were compared. These methods are titration ICP and XRF spectrometry techniques. The cerium oxide sample with estimated 45% cerium content needed to be digested and converted into solution before the analysis. The analytical results shown significantly no difference between each method. However, the titration method was found to be more convenient and suitable for quality control in the production of cerium oxide as it does not require standard cerium and the complicated analytical instruments

  3. Determination of the acidic sites of purified single-walled carbon nanotubes by acid base titration

    Science.gov (United States)

    Hu, H.; Bhowmik, P.; Zhao, B.; Hamon, M. A.; Itkis, M. E.; Haddon, R. C.

    2001-09-01

    We report the measurement of the acidic sites in three different samples of commercially available full-length purified single-walled carbon nanotubes (SWNTs) - as obtained from CarboLex (CLI), Carbon Solutions (CSI) and Tubes@Rice (TAR) - by simple acid-base titration methods. Titration of the purified SWNTs with NaOH and NaHCO 3 solutions was used to determine the total percentage of acidic sites and carboxylic acid groups, respectively. The total percentage of acidic sites in full length purified SWNTs from TAR, CLI and CSI are about 1-3%.

  4. Higher Order Inclusion Complexes and Secondary Interactions Studied by Global Analysis of Calorimetric Titrations

    DEFF Research Database (Denmark)

    Schönbeck, Jens Christian Sidney; Holm, René; Westh, Peter

    2012-01-01

    This paper investigates the use of isothermal titration calorimetry (ITC) as a tool for studying molecular systems in which weaker secondary interactions are present in addition to a dominant primary interaction. Such systems are challenging since the signal pertaining to the stronger primary...... results are validated by a 13C NMR titration and negative controls with a bile salt with no secondary binding site (glycocholate) (K = 2.96 ± 0.01 × 103 M–1). The method proved useful for detailed analysis of ITC data and may strengthen its use as a tool for studying molecular systems by advanced binding...

  5. Determination of fluoride ions in water by condutometric titration with lanthanum nitrates

    International Nuclear Information System (INIS)

    An alternative method for determining fluoride ions in drinking water by condutometric titration using La(NO3)3 as titrant is presented. The method is based on previous separation of fluoride from sample by distillation at 1350C. The pH of the distillated is adjusted between 5,5 - 6,0; ethanol is adicioned in 50% titrating the resultant solution with La(NO3)3. In these conditions, fluoride ions are determined with accuracy respectively, 5% and 4%. Natural samples of drinking water were analysed by this method and by the ion selective method, with agreement among the results. (author)

  6. Library Automation Style Guide.

    Science.gov (United States)

    Gaylord Bros., Liverpool, NY.

    This library automation style guide lists specific terms and names often used in the library automation industry. The terms and/or acronyms are listed alphabetically and each is followed by a brief definition. The guide refers to the "Chicago Manual of Style" for general rules, and a notes section is included for the convenience of individual…

  7. Automation in Warehouse Development

    NARCIS (Netherlands)

    Hamberg, R.; Verriet, J.

    2012-01-01

    The warehouses of the future will come in a variety of forms, but with a few common ingredients. Firstly, human operational handling of items in warehouses is increasingly being replaced by automated item handling. Extended warehouse automation counteracts the scarcity of human operators and support

  8. Automate functional testing

    Directory of Open Access Journals (Sweden)

    Ramesh Kalindri

    2014-06-01

    Full Text Available Currently, software engineers are increasingly turning to the option of automating functional tests, but not always have successful in this endeavor. Reasons range from low planning until over cost in the process. Some principles that can guide teams in automating these tests are described in this article.

  9. Automation in Immunohematology

    Directory of Open Access Journals (Sweden)

    Meenu Bajpai

    2012-01-01

    Full Text Available There have been rapid technological advances in blood banking in South Asian region over the past decade with an increasing emphasis on quality and safety of blood products. The conventional test tube technique has given way to newer techniques such as column agglutination technique, solid phase red cell adherence assay, and erythrocyte-magnetized technique. These new technologies are adaptable to automation and major manufacturers in this field have come up with semi and fully automated equipments for immunohematology tests in the blood bank. Automation improves the objectivity and reproducibility of tests. It reduces human errors in patient identification and transcription errors. Documentation and traceability of tests, reagents and processes and archiving of results is another major advantage of automation. Shifting from manual methods to automation is a major undertaking for any transfusion service to provide quality patient care with lesser turnaround time for their ever increasing workload. This article discusses the various issues involved in the process.

  10. Automated model building

    CERN Document Server

    Caferra, Ricardo; Peltier, Nicholas

    2004-01-01

    This is the first book on automated model building, a discipline of automated deduction that is of growing importance Although models and their construction are important per se, automated model building has appeared as a natural enrichment of automated deduction, especially in the attempt to capture the human way of reasoning The book provides an historical overview of the field of automated deduction, and presents the foundations of different existing approaches to model construction, in particular those developed by the authors Finite and infinite model building techniques are presented The main emphasis is on calculi-based methods, and relevant practical results are provided The book is of interest to researchers and graduate students in computer science, computational logic and artificial intelligence It can also be used as a textbook in advanced undergraduate courses

  11. Automation in Warehouse Development

    CERN Document Server

    Verriet, Jacques

    2012-01-01

    The warehouses of the future will come in a variety of forms, but with a few common ingredients. Firstly, human operational handling of items in warehouses is increasingly being replaced by automated item handling. Extended warehouse automation counteracts the scarcity of human operators and supports the quality of picking processes. Secondly, the development of models to simulate and analyse warehouse designs and their components facilitates the challenging task of developing warehouses that take into account each customer’s individual requirements and logistic processes. Automation in Warehouse Development addresses both types of automation from the innovative perspective of applied science. In particular, it describes the outcomes of the Falcon project, a joint endeavour by a consortium of industrial and academic partners. The results include a model-based approach to automate warehouse control design, analysis models for warehouse design, concepts for robotic item handling and computer vision, and auton...

  12. Advances in inspection automation

    Science.gov (United States)

    Weber, Walter H.; Mair, H. Douglas; Jansen, Dion; Lombardi, Luciano

    2013-01-01

    This new session at QNDE reflects the growing interest in inspection automation. Our paper describes a newly developed platform that makes the complex NDE automation possible without the need for software programmers. Inspection tasks that are tedious, error-prone or impossible for humans to perform can now be automated using a form of drag and drop visual scripting. Our work attempts to rectify the problem that NDE is not keeping pace with the rest of factory automation. Outside of NDE, robots routinely and autonomously machine parts, assemble components, weld structures and report progress to corporate databases. By contrast, components arriving in the NDT department typically require manual part handling, calibrations and analysis. The automation examples in this paper cover the development of robotic thickness gauging and the use of adaptive contour following on the NRU reactor inspection at Chalk River.

  13. 甘蔗糖蜜有机酸总量的电位滴定分析方法研究%Determination of total organic acids in sugar cane molasses with potentiometric titration

    Institute of Scientific and Technical Information of China (English)

    曹家兴; 陆建平; 李郁; 童张法

    2010-01-01

    甘蔗糖蜜试样溶液用HCl调节至pH值为2,加入乙酸指示羧酸滴定起点,用标准NaOH溶液进行电位滴定,突跃指数曲线指示出羧酸的滴定突跃起点和突跃终点,两突跃之间消耗的标准碱量相当于样品中羧酸的总量.无机酸包括硫酸或磷酸不影响滴定结果.方法平均样品加标回收率100.1%,相对标准偏差2.3%.测定了广西几家糖厂的糖蜜羧酸根总量,结果约为0.64mol/kg.

  14. 全自动电位滴定法测定混凝土中酸溶氯离子含量%DETERMINATION OF ACID-SOLUBLE CHLORIDE ION IN CONCRETE BY AUTOMATIC POTENTIOMETRIC TITRATION

    Institute of Scientific and Technical Information of China (English)

    吴双九; 徐晓云; 杨竞

    2009-01-01

    采用全自动电位滴定仪测定混凝土中氯离子含量,研究了实验相关影响因素.实验结果表明,pH值和AgNO3溶液浓度对试验结果无显著影响,在水溶液中加入乙醇有利于提高终点电位突跃,该方法加标回收率为96.9%~98.7%,测量结果的相对标准偏差为2.74%(n=6).

  15. Automatic Potentiometric Titration Determination of the Content of Ag in Ag2C2O4%自动电位滴定法测定草酸银中的银含量

    Institute of Scientific and Technical Information of China (English)

    王伟

    2015-01-01

    采用自动电位滴定法测定草酸银中的银含量,每个平行测定6次,滴定的相对标准偏差小于0.2%.方法的回收率为99.65 %~100.10%.经过对比实验证明,此方法操作简便快捷、准确可靠,不仅能满足生产过程中大批量草酸银中银含量的快速分析,而且不受干扰离子的影响.

  16. Integrated, paper-based potentiometric electronic tongue for the analysis of beer and wine.

    Science.gov (United States)

    Nery, Emilia Witkowska; Kubota, Lauro T

    2016-04-28

    The following manuscript details the stages of construction of a novel paper-based electronic tongue with an integrated Ag/AgCl reference, which can operate using a minimal amount of sample (40 μL). First, we optimized the fabrication procedure of silver electrodes, testing a set of different methodologies (electroless plating, use of silver nanoparticles and commercial silver paints). Later a novel, integrated electronic tongue system was assembled with the use of readily available materials such as paper, wax, lamination sheets, bleach etc. New system was thoroughly characterized and the ion-selective potentiometric sensors presented performance close to theoretical. An electronic tongue, composed of electrodes sensitive to sodium, calcium, ammonia and a cross-sensitive, anion-selective electrode was used to analyze 34 beer samples (12 types, 19 brands). This system was able to discriminate beers from different brands, and types, indicate presence of stabilizers and antioxidants, dyes or even unmalted cereals and carbohydrates added to the fermentation wort. Samples could be classified by type of fermentation (low, high) and system was able to predict pH and in part also alcohol content of tested beers. In the next step sample volume was minimalized by the use of paper sample pads and measurement in flow conditions. In order to test the impact of this advancement a four electrode system, with cross-sensitive (anion-selective, cation-selective, Ca(2+)/Mg(2+), K(+)/Na(+)) electrodes was applied for the analysis of 11 types of wine (4 types of grapes, red/white, 3 countries). Proposed matrix was able to group wines produced from different varieties of grapes (Chardonnay, Americanas, Malbec, Merlot) using only 40 μL of sample. Apart from that, storage stability studies were performed using a multimeter, therefore showing that not only fabrication but also detection can be accomplished by means of off-the-shelf components. This manuscript not only describes new

  17. Determination of Cobalt and Manganese percentages in paint driers by complex formation titration

    International Nuclear Information System (INIS)

    The use of paint can be seen in everyday life. However, authorities in many countries have laid down strict regulations on toxic metal content of paints for toys, domestic appliances and other applications. An insisting demand for quick and reliable monitoring techniques arose since. Driers, which are the main additive used in paints, contain heavy metals. Complex formation titration is carried out to determine the percentages of cobalt and manganese in different paint driers utilizing EDTA titration method. For cobalt determination, eight different samples were dissolved in an acetic acid solution diluted with ethanol and water, then treated with an excess of EDTA solution. PAN indicator was used as the metal indicator. The excess was titrated with cupric acid. The average cobalt content was 0.0710 %. The manganese-containing samples were a benzene-soluble and EDTA was used. Eight dissolved samples were treated with EDTA and then titrated with zinc chloride solution. Eriochrome Black-T was the indicator. The mean manganese content was 0.0431 %. (author)

  18. Titration of a Solid Acid Monitored by X-Ray Diffraction

    Science.gov (United States)

    Dungey, Keenan E.; Epstein, Paul

    2007-01-01

    An experiment is described to introduce students to an important class of solid-state reactions while reinforcing concepts of titration by using a pH meter and a powder X-ray diffractometer. The experiment was successful in teaching students the abstract concepts of solid-state structure and diffraction by applying the diffraction concepts learned…

  19. Solvatochromic Dyes as pH-Independent Indicators for Ionophore Nanosphere-Based Complexometric Titrations.

    Science.gov (United States)

    Zhai, Jingying; Xie, Xiaojiang; Bakker, Eric

    2015-12-15

    For half a century, complexometric titrations of metal ions have been performed with water-soluble chelators and indicators that typically require careful pH control. Very recently, ion-selective nanosphere emulsions were introduced that exhibit ion-exchange properties and are doped with lipophilic ionophores originally developed for chemical ion sensors. They may serve as novel, highly selective and pH independent complexometric reagents. While ion optode emulsions have been demonstrated as useful indicators for such titrations, they exhibit a pH cross-response that unfortunately complicates the identification of the end point. Here, we present pH-independent optode nanospheres as indicators for complexometric titrations, with calcium as an initial example. The nanospheres incorporate an ionic solvatochromic dye (SD), ion exchanger and ionophore. The solvatochromic dye will be only expelled from the core of the nanosphere into the aqueous solution at the end point at which point it results in an optical signal change. The titration curves are demonstrated to be pH-independent and with sharper end points than with previously reported chromoionophore-based optical nanospheres as indicator. The calcium concentration in mineral water was successfully determined using this method. PMID:26595520

  20. Effect of Spacers on CMCs and Micelle-forming Enthalpies of Gemini Surfactants by Titration Microcalorimetry

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The critical micelle concentrations (CMC) and the micelle-forming enthalpies (D Hmic) of gemini surfactants were first measured by the precise titration microcalorimetry. The results showed that D Hmic values are negative, and there is an exothermal minimum between s=4 and s=6. Furthermore, the CMCs of the surfactants are in good agreement with literature values.

  1. Charge Density Quantification of Polyelectrolyte Polysaccharides by Conductometric Titration: An Analytical Chemistry Experiment

    Science.gov (United States)

    Farris, Stefano; Mora, Luigi; Capretti, Giorgio; Piergiovanni, Luciano

    2012-01-01

    An easy analytical method for determination of the charge density of polyelectrolytes, including polysaccharides and other biopolymers, is presented. The basic principles of conductometric titration, which is used in the pulp and paper industry as well as in colloid and interface science, were adapted to quantify the charge densities of a…

  2. Isothermal titration calorimetry (ITC) study of surfactants and thermoresponsive poly-oxazolines

    Czech Academy of Sciences Publication Activity Database

    Bogomolova, Anna; Filippov, Sergey K.; Starovoytova, Larisa; Sedláček, Ondřej; Macková, Hana; Hrubý, Martin; Štěpánek, Petr

    Pisa : European Polymer Federation, 2013. P6-13. [European Polymer Congress - EPF 2013. 16.06.2013-21.06.2013, Pisa] Grant ostatní: AV ČR(CZ) M200501201 Institutional support: RVO:61389013 Keywords : isothermal titration calorimetry (ITC) * poly-oxyzolines Subject RIV: CD - Macromolecular Chemistry

  3. Subsite binding energies of an exo-polygalacturonase using isothermal titration calorimetry

    Science.gov (United States)

    Thermodynamic parameters for binding of a series of galacturonic acid oligomers to an exo-polygalacturonase, RPG16 from Rhizopus oryzae, were determined by isothermal titration calorimetry. Binding of oligomers varying in chain length from two to five galacturonic acid residues is an exothermic proc...

  4. Role of titrated low dose oral misoprostol solution in induction of labour

    Directory of Open Access Journals (Sweden)

    Sarvottma Antil

    2016-03-01

    Conclusions: For induction of labour in women with term gestation after cervical priming, low dose oral misoprostol solution in titrated doses and intravenous oxytocin were found to be comparable with each other in terms of labour outcomes, efficacy and adverse effects. [Int J Reprod Contracept Obstet Gynecol 2016; 5(3.000: 775-782

  5. Thermodynamic profiling of Peptide membrane interactions by isothermal titration calorimetry: a search for pores and micelles

    DEFF Research Database (Denmark)

    Henriksen, Jonas Rosager; Andresen, Thomas Lars

    2011-01-01

    mixed peptide-lipid micelles. We have investigated the mode of action of the antimicrobial peptide mastoparan-X using isothermal titration calorimetry (ITC) and cryo-transmission electron microscopy (cryo-TEM). The results show that mastoparan-X induces a range of structural transitions of POPC/POPG (3...

  6. A modelling approach to establish experimental parameters of a flow-through titration

    NARCIS (Netherlands)

    Reijnders, H.F.R.; Staden, J.J. van; Eelderink, G.H.B; Griepink, B.

    1980-01-01

    A flow-through titrimeter with optical detection and the flow-through titration of sulphate have been studied by using control engineering methods. Qualitative chemical descriptions and systems analysis yield a model covering different precipitation rates of barium sulphate. The validity of the mode

  7. ELECTROKINETIC PHENOMENA : VII. RELATIONSHIP BETWEEN ELECTRIC MOBILITY, CHARGE, TITRATION CURVE, AND OPTICAL ROTATION OF PROTEIN.

    Science.gov (United States)

    Abramson, H A; Grossman, E B

    1932-05-20

    The specific rotation of egg albumin, gliadin, and gelatin (40 degrees C.) is discussed in connection with available data on (a) mobility, (b) titration curve, and (c) osmotic pressure. It seems likely that the change in specific rotation with pH of protein solutions is proportional to the change in net charge. PMID:19872669

  8. Coulometric Titration of Ethylenediaminetetraacetate (EDTA) with Spectrophotometric Endpoint Detection: An Experiment for the Instrumental Analysis Laboratory

    Science.gov (United States)

    Williams, Kathryn R.; Young, Vaneica Y.; Killian, Benjamin J.

    2011-01-01

    Ethylenediaminetetraacetate (EDTA) is commonly used as an anticoagulant in blood-collection procedures. In this experiment for the instrumental analysis laboratory, students determine the quantity of EDTA in commercial collection tubes by coulometric titration with electrolytically generated Cu[superscript 2+]. The endpoint is detected…

  9. Isothermal Titration Calorimetry and Macromolecular Visualization for the Interaction of Lysozyme and Its Inhibitors

    Science.gov (United States)

    Wei, Chin-Chuan; Jensen, Drake; Boyle, Tiffany; O'Brien, Leah C.; De Meo, Cristina; Shabestary, Nahid; Eder, Douglas J.

    2015-01-01

    To provide a research-like experience to upper-division undergraduate students in a biochemistry teaching laboratory, isothermal titration calorimetry (ITC) is employed to determine the binding constants of lysozyme and its inhibitors, N-acetyl glucosamine trimer (NAG[subscript 3]) and monomer (NAG). The extremely weak binding of lysozyme/NAG is…

  10. The Quantitative Resolution of a Mixture of Group II Metal Ions by Thermometric Titration with EDTA. An Analytical Chemistry Experiment.

    Science.gov (United States)

    Smith, Robert L.; Popham, Ronald E.

    1983-01-01

    Presents an experiment in thermometric titration used in an analytic chemistry-chemical instrumentation course, consisting of two titrations, one a mixture of calcium and magnesium, the other of calcium, magnesium, and barium ions. Provides equipment and solutions list/specifications, graphs, and discussion of results. (JM)

  11. Hydrogen-ion titrations of amino acids and proteins in solutions containing concentrated electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Fergg, F. [Technische Universitaet Muenchen (Germany); Kuehner, D.E.; Blanch, H.W.; Prausnitz, J.M. [Lawrence Berkeley Lab., CA (United States)

    1994-12-01

    This report describes a first attempt to quantify the net charge as a function of solution pH for lysozyme and {alpha}-chymotrypsin at 0.1 M, 1.0 M and 3.0 M ionic strength, (IS). The calculations are based on the residue (titratable group) pK{sub a}`s in the amino-acid sequence of the protein. To determine these pK{sub a}`s, a simple theory was used which assumes that the pK{sub a}`s are independent from each other in the protein and are equal to their pK{sub a} values in free amino-acid solution (Independent-Site Theory, IST). Residue pK{sub a}`s were obtained from amino-acid hydrogen-ion titrations at three different KCl concentrations corresponding to 0.1M, 1.0M and 3.0M ionic strength. After construction of a suitable apparatus, the experimental procedure and data reduction were computerized to perform a large number of titrations. Most measured pK{sub a}`s showed high reproducibility (the difference of pK{sub a} values observed between two experiments was less than 0.05). For IS = 0.1M, observed pK{sub a}`s agreed with literature values to within a few hundredths of a pH unit. Furthermore, the ionic-strength dependence of the pK{sub a}`s followed the trends reported in the literature, viz. pK{sub a} values decrease with increasing ionic strength until they reach a minimum at about IS = 0.5M. At still higher IS, pK{sub a}`s increase as the ionic strength rises to 3M. The known pK{sub a}`s of all titratable groups in a protein were used with the IST to give a first approximation of how the protein net charge varies with pH at high ionic strength. A comparison of the titration curves based on the IST with experimental lysozyme and {alpha}-chymotrypsin titration data indicates acceptable agreement at IS = 0.1M. However, comparison of measured and calculated titration curves at IS = 1M and IS = 3M indicates only quantitative agreement.

  12. Fully automated measuring equipment for aqueous boron and its application to online monitoring of industrial process effluents.

    Science.gov (United States)

    Ohyama, Seiichi; Abe, Keiko; Ohsumi, Hitoshi; Kobayashi, Hirokazu; Miyazaki, Naotsugu; Miyadera, Koji; Akasaka, Kin-ichi

    2009-06-01

    Fully automated measuring equipment for aqueous boron (referred to as the online boron monitor) was developed on the basis of a rapid potentiometric determination method using a commercial BF4(-) ion-selective electrode (ISE). The equipment can measure boron compounds with concentration ranging from a few to several hundred mg/L, and the measurement is completed in less than 20 min without any pretreatment of the sample. In the monitor, a series of operations for the measurement, i.e., sampling and dispensing of the sample, addition of the chemicals, acquisition and processing of potentiometric data, rinsing of the measurement cell, and calibration of the BF4(-) ISE, is automated. To demonstrate the performance, we installed the monitor in full-scale coal-fired power plants and measured the effluent from a flue gas desulfurization unit. The boron concentration in the wastewater varied significantly depending on the type of coal and the load of power generation. An excellent correlation (R2 = 0.987) was obtained in the measurements between the online boron monitor and inductively coupled plasma atomic emission spectrometry, which proved that the developed monitor can serve as a useful tool for managing boron emission in industrial process effluent. PMID:19569339

  13. Improvement of Test Automation

    OpenAIRE

    Räsänen, Timo

    2013-01-01

    The purpose for this study was to find out how to ensure that the automated testing of MME in the Network Verification will continue smooth and reliable while using the in-house developed test automation framework. The goal of this thesis was to reveal the reasons of the currently challenging situation and to find the key elements to be improved in the MME testing carried by the test automation. Also a reason for the study was to get solutions as to how to change the current procedures and wa...

  14. Chef infrastructure automation cookbook

    CERN Document Server

    Marschall, Matthias

    2013-01-01

    Chef Infrastructure Automation Cookbook contains practical recipes on everything you will need to automate your infrastructure using Chef. The book is packed with illustrated code examples to automate your server and cloud infrastructure.The book first shows you the simplest way to achieve a certain task. Then it explains every step in detail, so that you can build your knowledge about how things work. Eventually, the book shows you additional things to consider for each approach. That way, you can learn step-by-step and build profound knowledge on how to go about your configuration management

  15. Technical Note: Maximising accuracy and minimising cost of a potentiometrically regulated ocean acidification simulation system

    Science.gov (United States)

    MacLeod, C. D.; Doyle, H. L.; Currie, K. I.

    2014-05-01

    This article describes a potentiometric ocean acidification simulation system which automatically regulates pH through the injection of 100% CO2 gas into temperature-controlled seawater. The system is ideally suited to long-term experimental studies of the effect of acidification on biological processes involving small-bodied (10-20 mm) calcifying or non-calcifying organisms. Using hobbyist grade equipment, the system was constructed for approximately USD 1200 per treatment unit (tank, pH regulation apparatus, chiller, pump/filter unit). An overall accuracy of ±0.05 pHT units (SD) was achieved over 90 days in two acidified treatments (7.60 and 7.40) at 12 °C using glass electrodes calibrated with salt water buffers, thereby preventing liquid junction error. The accuracy of the system was validated through the independent calculation of pHT (12 °C) using dissolved inorganic carbon (DIC) and total alkalinity (AT) data taken from discrete acidified seawater samples. The system was used to compare the shell growth of the marine gastropod Zeacumantus subcarinatus infected with the trematode parasite Maritrema novaezealandensis with that of uninfected snails, at pH levels of 7.4, 7.6, and 8.1.

  16. Manganese(III Porphyrin-based Potentiometric Sensors for Diclofenac Assay in Pharmaceutical Preparations

    Directory of Open Access Journals (Sweden)

    Eugenia Fagadar-Cosma

    2010-09-01

    Full Text Available Two manganese(III porphyrins: manganese(III tetraphenylporphyrin chloride and manganese(III-tetrakis(3-hydroxyphenylporphyrin chloride were tested as ionophores for the construction of new diclofenac−selective electrodes. The electroactive material was incorporated either in PVC or a sol−gel matrix. The effect of different plasticizers and additives (anionic and cationic on the potentiometric response was studied. The best results were obtained for the PVC membrane plasticized with dioctylphtalate and having sodium tetraphenylborate as a lipophilic anionic additive incorporated. The sensor response was linear in the concentration range 3 × 10−6 – 1 × 10−2 M with a slope of −59.7 mV/dec diclofenac, a detection limit of 1.5 × 10−6 M and very good selectivity coefficients. It was used for the determination of diclofenac in pharmaceutical preparations, by direct potentiometry. The results were compared with those obtained by the HPLC reference method and a good agreement was found between the two methods.

  17. Manganese(III) porphyrin-based potentiometric sensors for diclofenac assay in pharmaceutical preparations.

    Science.gov (United States)

    Vlascici, Dana; Pruneanu, Stela; Olenic, Liliana; Pogacean, Florina; Ostafe, Vasile; Chiriac, Vlad; Pica, Elena Maria; Bolundut, Liviu Calin; Nica, Luminita; Fagadar-Cosma, Eugenia

    2010-01-01

    Two manganese(III) porphyrins: manganese(III) tetraphenylporphyrin chloride and manganese(III)-tetrakis(3-hydroxyphenyl)porphyrin chloride were tested as ionophores for the construction of new diclofenac-selective electrodes. The electroactive material was incorporated either in PVC or a sol-gel matrix. The effect of different plasticizers and additives (anionic and cationic) on the potentiometric response was studied. The best results were obtained for the PVC membrane plasticized with dioctylphtalate and having sodium tetraphenylborate as a lipophilic anionic additive incorporated. The sensor response was linear in the concentration range 3 × 10(-6) - 1 × 10(-2) M with a slope of -59.7 mV/dec diclofenac, a detection limit of 1.5 × 10(-6) M and very good selectivity coefficients. It was used for the determination of diclofenac in pharmaceutical preparations, by direct potentiometry. The results were compared with those obtained by the HPLC reference method and a good agreement was found between the two methods. PMID:22163384

  18. Trace detection and discrimination of explosives using electrochemical potentiometric gas sensors.

    Science.gov (United States)

    Sekhar, Praveen K; Brosha, Eric L; Mukundan, Rangachary; Linker, Kevin L; Brusseau, Charles; Garzon, Fernando H

    2011-06-15

    In this article, selective and sensitive detection of trace amounts of pentaerythritol tetranitrate (PETN), 2,4,6-trinitrotoluene (TNT) and cyclotrimethylenetrinitramine (RDX) is demonstrated. The screening system is based on a sampling/concentrator front end and electrochemical potentiometric gas sensors as the detector. Preferential hydrocarbon and nitrogen oxide(s) mixed potential sensors based on lanthanum strontium chromite and Pt electrodes with yttria stabilized zirconia (YSZ) solid electrolyte were used to capture the signature of the explosives. Quantitative measurements based on hydrocarbon and nitrogen oxide sensor responses indicated that the detector sensitivity scaled proportionally with the mass of the explosives (1-3 μg). Moreover, the results showed that PETN, TNT, and RDX samples could be discriminated from each other by calculating the ratio of nitrogen oxides to hydrocarbon integrated area under the peak. Further, the use of front-end technology to collect and concentrate the high explosive (HE) vapors make intrinsically low vapor pressure of the HE less of an obstacle for detection while ensuring higher sensitivity levels. In addition, the ability to use multiple sensors each tuned to basic chemical structures (e.g., nitro, amino, peroxide, and hydrocarbon groups) in HE materials will permit the construction of low-cost detector systems for screening a wide spectrum of explosives with lower false positives than present-day technologies. PMID:21435779

  19. Indicator electrodes from d-elements for application in different types of potentiometric analytical methods

    Directory of Open Access Journals (Sweden)

    Z. Kunasheva

    2012-05-01

    Full Text Available The article covers the use of metal electrodes from titanium, tungsten, molybdenum as indicator electrodes at potentiometric method of analysis. The condition of measuring operation in dependence on pH, ionic strength of solutions is described in the article. Electrode potential of testing electrodes are measured in the interval of concentration of salts from 0,1∙10-1 mole/l till 0,1∙10-6 mole/l. The results of testing of electrical-analytical description of metal electrodes made of d-elements, in particular, titanium, tungsten, molybdenum in solutions of cations of some metals and anions were mentioned. As ions of metal cations Cu2+, Cd2+, Zn2+, Pb2+ and anions Cl-, I-, F- were chosen.It is identified that titanic electrode has different response to ions of copper (II, zinc and cadmium. However, dependence of electrode potential on concentration of ions of metal is rectilinear, that is vequired of indicator electrodes in the direct potential metrics.  

  20. Potentiometric and spectrophotometric studies of the complexation of Schiff-base hydrazones containing the pyrimidine moiety

    Directory of Open Access Journals (Sweden)

    M. SHEBL

    2003-10-01

    Full Text Available Three Schiff-base hydrazones (ONN – donors were prepared by condensation of 2-amino-4-hydrazino-6-methylpyrimidine with 2-hydroxyacetophenone, 2-methoxybenzaldehyde and diacetyl to yield 2-OHAHP, 2-OMeBHP and DHP, respectively. The structures of these ligands were elucidated by elemental analysis, UV, IR, 1H-NMR and mass spectra. The metal–ligand stability constants of Mn2+, Fe3+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, UO22+ and Th4+ chelates were determined potentiometrically in two different media (75 % (v/v dioxane–water and ethanol–water at 283, 293, 303 and 313 K at an ionic strength of 0.05 M (KNO3. The thermodynamic parameters of the 1:1 and 1:2 complexes were evaluated and are discussed. The dissociation constants of 2-OHAHP, 2-OMeBHP and DHP ligands and the stability constants of Co2+, Ni2+ and Cu2+ with 2-OHAHP were determined spectrophotometrically in 75 % (v/v dioxane–water.

  1. Technical Note: Maximising accuracy and minimising cost of a potentiometrically regulated ocean acidification simulation system

    Directory of Open Access Journals (Sweden)

    C. D. MacLeod

    2014-05-01

    Full Text Available This article describes a potentiometric ocean acidification simulation system which automatically regulates pH through the injection of 100% CO2 gas into temperature-controlled seawater. The system is ideally suited to long-term experimental studies of the effect of acidification on biological processes involving small-bodied (10–20 mm calcifying or non-calcifying organisms. Using hobbyist grade equipment, the system was constructed for approximately USD 1200 per treatment unit (tank, pH regulation apparatus, chiller, pump/filter unit. An overall accuracy of ±0.05 pHT units (SD was achieved over 90 days in two acidified treatments (7.60 and 7.40 at 12 °C using glass electrodes calibrated with salt water buffers, thereby preventing liquid junction error. The accuracy of the system was validated through the independent calculation of pHT (12 °C using dissolved inorganic carbon (DIC and total alkalinity (AT data taken from discrete acidified seawater samples. The system was used to compare the shell growth of the marine gastropod Zeacumantus subcarinatus infected with the trematode parasite Maritrema novaezealandensis with that of uninfected snails, at pH levels of 7.4, 7.6, and 8.1.

  2. A Potentiometric Formaldehyde Biosensor Based on Immobilization of Alcohol Oxidase on Acryloxysuccinimide-modified Acrylic Microspheres

    Directory of Open Access Journals (Sweden)

    Lee Yook Heng

    2010-11-01

    Full Text Available A new alcohol oxidase (AOX enzyme-based formaldehyde biosensor based on acrylic microspheres has been developed. Hydrophobic poly(n-butyl acrylate-N-acryloxy-succinimide [poly(nBA-NAS] microspheres, an enzyme immobilization matrix, was synthesized using photopolymerization in an emulsion form. AOX-poly(nBA-NAS microspheres were deposited on a pH transducer made from a layer of photocured and self-plasticized polyacrylate membrane with an entrapped pH ionophore coated on a Ag/AgCl screen printed electrode (SPE. Oxidation of formaldehyde by the immobilized AOX resulted in the production of protons, which can be determined via the pH transducer. Effects of buffer concentrations, pH and different amount of immobilization matrix towards the biosensor’s analytical performance were investigated. The formaldehyde biosensor exhibited a dynamic linear response range to formaldehyde from 0.3–316.2 mM and a sensitivity of 59.41 ± 0.66 mV/decade (R2 = 0.9776, n = 3. The lower detection limit of the biosensor was 0.3 mM, while reproducibility and repeatability were 3.16% RSD (relative standard deviation and 1.11% RSD, respectively (n = 3. The use of acrylic microspheres in the potentiometric formaldehyde biosensor improved the biosensor’s performance in terms of response time, linear response range and long term stability when compared with thick film immobilization methods.

  3. Automated Vehicles Symposium 2014

    CERN Document Server

    Beiker, Sven; Road Vehicle Automation 2

    2015-01-01

    This paper collection is the second volume of the LNMOB series on Road Vehicle Automation. The book contains a comprehensive review of current technical, socio-economic, and legal perspectives written by experts coming from public authorities, companies and universities in the U.S., Europe and Japan. It originates from the Automated Vehicle Symposium 2014, which was jointly organized by the Association for Unmanned Vehicle Systems International (AUVSI) and the Transportation Research Board (TRB) in Burlingame, CA, in July 2014. The contributions discuss the challenges arising from the integration of highly automated and self-driving vehicles into the transportation system, with a focus on human factors and different deployment scenarios. This book is an indispensable source of information for academic researchers, industrial engineers, and policy makers interested in the topic of road vehicle automation.

  4. I-94 Automation FAQs

    Data.gov (United States)

    Department of Homeland Security — In order to increase efficiency, reduce operating costs and streamline the admissions process, U.S. Customs and Border Protection has automated Form I-94 at air and...

  5. Automated Vehicles Symposium 2015

    CERN Document Server

    Beiker, Sven

    2016-01-01

    This edited book comprises papers about the impacts, benefits and challenges of connected and automated cars. It is the third volume of the LNMOB series dealing with Road Vehicle Automation. The book comprises contributions from researchers, industry practitioners and policy makers, covering perspectives from the U.S., Europe and Japan. It is based on the Automated Vehicles Symposium 2015 which was jointly organized by the Association of Unmanned Vehicle Systems International (AUVSI) and the Transportation Research Board (TRB) in Ann Arbor, Michigan, in July 2015. The topical spectrum includes, but is not limited to, public sector activities, human factors, ethical and business aspects, energy and technological perspectives, vehicle systems and transportation infrastructure. This book is an indispensable source of information for academic researchers, industrial engineers and policy makers interested in the topic of road vehicle automation.

  6. Hydrometeorological Automated Data System

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The Office of Hydrologic Development of the National Weather Service operates HADS, the Hydrometeorological Automated Data System. This data set contains the last...

  7. An automated Certification Authority

    CERN Document Server

    Shamardin, L V

    2002-01-01

    This note describe an approach to building an automated Certification Authority. It is compatible with basic requirements of RFC2527. It also supports Registration Authorities and Globus Toolkit grid-cert-renew automatic certificate renewal.

  8. Disassembly automation automated systems with cognitive abilities

    CERN Document Server

    Vongbunyong, Supachai

    2015-01-01

    This book presents a number of aspects to be considered in the development of disassembly automation, including the mechanical system, vision system and intelligent planner. The implementation of cognitive robotics increases the flexibility and degree of autonomy of the disassembly system. Disassembly, as a step in the treatment of end-of-life products, can allow the recovery of embodied value left within disposed products, as well as the appropriate separation of potentially-hazardous components. In the end-of-life treatment industry, disassembly has largely been limited to manual labor, which is expensive in developed countries. Automation is one possible solution for economic feasibility. The target audience primarily comprises researchers and experts in the field, but the book may also be beneficial for graduate students.

  9. Automated security management

    CERN Document Server

    Al-Shaer, Ehab; Xie, Geoffrey

    2013-01-01

    In this contributed volume, leading international researchers explore configuration modeling and checking, vulnerability and risk assessment, configuration analysis, and diagnostics and discovery. The authors equip readers to understand automated security management systems and techniques that increase overall network assurability and usability. These constantly changing networks defend against cyber attacks by integrating hundreds of security devices such as firewalls, IPSec gateways, IDS/IPS, authentication servers, authorization/RBAC servers, and crypto systems. Automated Security Managemen

  10. Automating Supplier Selection Procedures

    OpenAIRE

    Davidrajuh, Reggie

    2001-01-01

    This dissertation describes a methodology, tools, and implementation techniques of automating supplier selection procedures of a small and medium-sized agile virtual enterprise. Firstly, a modeling approach is devised that can be used to model the supplier selection procedures of an enterprise. This modeling approach divides the supplier selection procedures broadly into three stages, the pre-selection, selection, and post-selection stages. Secondly, a methodology is presented for automating ...

  11. Taiwan Automated Telescope Network

    OpenAIRE

    Shuhrat Ehgamberdiev; Alexander Serebryanskiy; Antonio Jimenez; Li-Han Wang; Ming-Tsung Sun; Javier Fernandez Fernandez; Dean-Yi Chou

    2010-01-01

    A global network of small automated telescopes, the Taiwan Automated Telescope (TAT) network, dedicated to photometric measurements of stellar pulsations, is under construction. Two telescopes have been installed in Teide Observatory, Tenerife, Spain and Maidanak Observatory, Uzbekistan. The third telescope will be installed at Mauna Loa Observatory, Hawaii, USA. Each system uses a 9-cm Maksutov-type telescope. The effective focal length is 225 cm, corresponding to an f-ratio of 25. The field...

  12. Automated Lattice Perturbation Theory

    Energy Technology Data Exchange (ETDEWEB)

    Monahan, Christopher

    2014-11-01

    I review recent developments in automated lattice perturbation theory. Starting with an overview of lattice perturbation theory, I focus on the three automation packages currently "on the market": HiPPy/HPsrc, Pastor and PhySyCAl. I highlight some recent applications of these methods, particularly in B physics. In the final section I briefly discuss the related, but distinct, approach of numerical stochastic perturbation theory.

  13. Automated functional software testing

    OpenAIRE

    Jelnikar, Kristina

    2009-01-01

    The following work describes an approach to software test automation of functional testing. In the introductory part we are introducing what testing problems development companies are facing. The second chapter describes some testing methods, what role does testing have in software development, some approaches to software development and the meaning of testing environment. Chapter 3 is all about test automation. After a brief historical presentation, we are demonstrating through s...

  14. Instant Sikuli test automation

    CERN Document Server

    Lau, Ben

    2013-01-01

    Get to grips with a new technology, understand what it is and what it can do for you, and then get to work with the most important features and tasks. A concise guide written in an easy-to follow style using the Starter guide approach.This book is aimed at automation and testing professionals who want to use Sikuli to automate GUI. Some Python programming experience is assumed.

  15. Comparison of 3 titration methods of positive airway pressure for obstructive sleep apnea syndrome: a random, single-blind and self-control clinical study

    OpenAIRE

    LI Yan; Liu, Xin-Xin; Wan-er WANG; Wang, Yang; Gao, He

    2013-01-01

    Objective  To evaluate the efficacy and safety of polysomnography-manual continuous positive airway pressure titration (PSG-CPAP), polysomnography-automatic positive airway pressure titration (PSG-APAP), or automatic positive airway pressure titration (APAP) in patients with moderate or severe simple obstructive sleep apnea syndrome (OSAS). Methods  Twenty patients with moderate or severe OSAS sequentially underwent PSG-CPAP, PSG-APAP and APAP titration 3 days apart, and then 3 primary effica...

  16. Highly selective electrode for potentiometric analysis of methadone in biological fluids and pharmaceutical formulations.

    Science.gov (United States)

    Ardeshiri, Moslem; Jalali, Fahimeh

    2016-06-01

    In order to develop a fast and simple procedure for methadone analysis in biological fluids, a graphite paste electrode (GPE) was modified with the ion-pair of methadone-phosphotungstic acid, and multiwalled carbon nanotubes (MWCNTs). Optimized composition of the electrode with respect to graphite powder:paraffin oil:MWCNTs:ion pair, was 58:30:8:4 (w/w%). The electrode showed a near-Nernstian slope of 58.9±0.3mV/decade for methadone in a wide linear range of 1.0×10(-8)-4.6×10(-3)M, with a detection limit of 1.0×10(-8)M. The electrode response was independent of pH in the range of 5-11, with a fast response time (~4s) at 25°C. The sensor showed high selectivity and was successfully applied to the determination of sub-micromolar concentrations of methadone in human blood serum and urine samples, with recoveries in the range of 95-99.8%. The average recovery of methadone from tablets (5mg/tablet) by using the proposed method was 98%. The life time of the modified electrode was more than 5months, due to the characteristic of GPE which can be cut off and fresh electrode surface be available. A titration procedure was performed for methadone analysis by using phosphotungstic acid, as titrating agent, which showed an accurate end point and 1:1 stoichiometry for the ion-pair formed (methadone:phosphotungstic acid). The simple and rapid procedure as well as excellent detection limit and selectivity are some of the advantages of the proposed sensor for methadone. PMID:27040192

  17. Development of a potentiometric EDTA method for determination of molybdenum. Use of the analysis for molybdenite concentrates

    Science.gov (United States)

    Khristova, R.; Vanmen, M.

    1986-01-01

    Based on considerations of principles and experimental data, the interference of sulfate ions in poteniometric titration of EDTA with FeCl3 was confirmed. The method of back complexometric titration of molybdenum of Nonova and Gasheva was improved by replacing hydrazine sulfate with hydrazine hydrochloride for reduction of Mo(VI) to Mo(V). The method can be used for one to tenths of mg of molybdenum with 0.04 mg standard deviation. The specific method of determination of molybdenum in molybdenite concentrates is presented.

  18. Development of a potentiometric EDTA method for determination of molybdenum. Use of the analysis for molybdenite concentrates

    International Nuclear Information System (INIS)

    Based on considerations of principles and experimental data, the interference of sulfate ions in poteniometric titration of EDTA with FeCl3 was confirmed. The method of back complexometric titration of molybdenum of Nonova and Gasheva was improved by replacing hydrazine sulfate with hydrazine hydrochloride for reduction of Mo(VI) to Mo(V). The method can be used for one to tenths of mg of molybdenum with 0.04 mg standard deviation. The specific method of determination of molybdenum in molybdenite concentrates is presented

  19. Rapid determination of phenolic compounds in water samples by alternating-current oscillopolarographic titration

    Institute of Scientific and Technical Information of China (English)

    XIAO Jun-ping; WANG Xue-feng; ZHOU Qing-xiang; FAN Xiao-yuan; SU Xian-fa; Bai Hua-hua; DUAN Hai-jing

    2007-01-01

    A rapid, simple and sensitive method was demonstrated for the determination of phenolic compounds in water samples by alternating-current oscillopolarographic titration. With the presence of sulfuric acid, phenol could be transferred into a nitroso-compound by reacting with NaNO2. The titration end-point was obtained by the formation of a sharp cut in the oscillopolarographic with infinitesimal NaNO2 on double platinum electrodes. The results showed that phenol had an excellent linear relationship over the range of 4.82×10-6 -9.65×10-3 mol/L, the RSD of the proposed method was lower than 1.5%, and the spiked recoveries of three real water samples were in the range of 95.6%-106.9%.

  20. Titratable macroions in multivalent electrolyte solutions: Strong coupling dressed ion approach

    Science.gov (United States)

    Adžić, Nataša; Podgornik, Rudolf

    2016-06-01

    We present a theoretical description of the effect of polyvalent ions on the interaction between titratable macroions. The model system consists of two point-like macroions with dissociable sites, immersed in an asymmetric ionic mixture of monovalent and polyvalent salts. We formulate a dressed ion strong coupling theory, based on the decomposition of the asymmetric ionic mixture into a weakly electrostatically coupled monovalent salt and into polyvalent ions that are strongly electrostatically coupled to the titratable macro-ions. The charge of the macroions is not considered as fixed, but is allowed to respond to local bathing solution parameters (electrostatic potential, pH of the solution, and salt concentration) through a simple charge regulation model. The approach presented, yielding an effective polyvalent-ion mediated interaction between charge-regulated macroions at various solution conditions, describes the strong coupling equivalent of the Kirkwood-Schumaker interaction.

  1. Successful management of a difficult cancer pain patient by appropriate adjuvant and morphine titration

    Directory of Open Access Journals (Sweden)

    Shiv PS Rana

    2011-01-01

    Full Text Available Morphine has been used for many years to relieve cancer pain. Oral morphine (in either immediate release or modified release form remains the analgesic of choice for moderate or severe cancer pain. The dose of oral morphine is titrated up to achieve adequate relief from pain with minimal side effects. Antidepressant and anticonvulsant drugs, when used in addition to conventional analgesics, give excellent relief from cancer pain. Most cancer pain responds to pharmacological measures with oral morphine but some pain like neuropathic and bony pain, pain in children and elderly age group, and advanced malignancy pain are very difficult to treat. Here, we report the management of a similar patient of severe cancer pain and the difficulty that we came across during dose titration of oral morphine and adjuvant analgesic.

  2. An automatic system for acidity determination based on sequential injection titration and the monosegmented flow approach.

    Science.gov (United States)

    Kozak, Joanna; Wójtowicz, Marzena; Gawenda, Nadzieja; Kościelniak, Paweł

    2011-06-15

    An automatic sequential injection system, combining monosegmented flow analysis, sequential injection analysis and sequential injection titration is proposed for acidity determination. The system enables controllable sample dilution and generation of standards of required concentration in a monosegmented sequential injection manner, sequential injection titration of the prepared solutions, data collecting, and handling. It has been tested on spectrophotometric determination of acetic, citric and phosphoric acids with sodium hydroxide used as a titrant and phenolphthalein or thymolphthalein (in the case of phosphoric acid determination) as indicators. Accuracy better than |4.4|% (RE) and repeatability better than 2.9% (RSD) have been obtained. It has been applied to the determination of total acidity in vinegars and various soft drinks. The system provides low sample (less than 0.3 mL) consumption. On average, analysis of a sample takes several minutes. PMID:21641455

  3. 滴定分析教学的好帮手"Titration simulator"

    Institute of Scientific and Technical Information of China (English)

    "Titration; simulator"--Good; assistant; for; titration; analysis

    2005-01-01

      Titration simulator(滴定模拟器)软件是专门为滴定分析而设计的教学软件,它短小精悍,简洁实用,可以从Internet网上免费下载,网址为:http://www.chemonline.net/Truechemsoft/downsoft.asp?softID=1565该软件所占容量仅为72KB,是学生训练及化学教师的好助手.笔者在教学中尝试运用该软件辅助教学,效果良好,现将Titration simulator软件的主要功能、应用简要介绍如下:……

  4. Titratable Macroions in Multivalent Electrolyte Solutions: Strong Coupling Dressed Ion Approach

    CERN Document Server

    Adzic, Natasa

    2016-01-01

    We present a theoretical description of the effect of polyvalent ions on the interaction between titratable macro-ions. The model system consists of two point-like macro-ions with dissociable sites, immersed in an asymmetric ionic mixture of monovalent and polyvalent salts. We formulate a {\\em dressed ion strong coupling theory}, based on the decomposition of the asymmetric ionic mixture into a weakly electrostatically coupled monovalent salt, and into polyvalent ions that are strongly electrostatically coupled to the titratable macro-ions. The charge of the macroions is not considered as fixed, but is allowed to respond to local bathing solution parameters (electrostatic potential, $pH$ of the solution, salt concentration) through a simple {\\em charge regulation} model. The approach presented, yielding an effective polyvalent-ion mediated interaction between charge-regulated macro-ions at various solution conditions, describes the strong coupling equivalent of the Kirkwood-Schumaker interaction.

  5. Development of analytical method for the determination of uranium in presence of plutonium by complexometric titration

    International Nuclear Information System (INIS)

    Uranium determination in the plant samples by conventional Davies Gray method generates radioactive wastes bearing plutonium. Uranium determination by complexometric titration using 2,6 Pyridine di-carboxylic acid (PDCA) as titrant is a well established. It had been observed that the presence of plutonium increases bias in the determination of uranium. Hence for the Plutonium bearing process samples such as strip products, feed samples of the Plutonium reconversion, Uranium estimation through PDCA method is optimized by employing ethylene diamine tetra acetic (EDTA) as the masking agent. It is found that beyond 0.075 m moles of EDTA bias for determination of uranium increased; therefore EDTA of 0.05 mmoles is maintained in the titration medium. The precision for determination of uranium in absence of Pu for a range of 3-10 mg was found be less than 0.5 %. A bias of 6 % is observed for uranium determination with two different ratios of U and Pu. (author)

  6. Potentiometric CO2 Sensor Using Li Ion Conducting Li3PO4Thin Film Electrolyte

    Directory of Open Access Journals (Sweden)

    Jin Seong Park

    2005-11-01

    Full Text Available Li+ ion conducting Li3PO4 thin film electrolytes with thickness 300nm, 650nm and1.2μm were deposited on Al2O3 substrate at room temperature by thermal evaporation method.Reference and sensing electrodes were printed on Au interfaces by conventional screen printingtechnique. The overall dimension of the sensor was 3 x 3 mm and of electrodes were 1 x 1.5 mmeach. The fabricated solid state potentiometric CO2 sensors of type: CO2, O2, Au, Li2TiO3-TiO2 / Li3PO4 / Li2CO3, Au, CO2, O2 have been investigated for CO2 sensing properties. Theelectromotive force (emf and δemf/dec values of the sensors are dependent on the thickness ofthe electrolyte film. 1.2μm thickness deposited sensor has shown good sensing behavior than thesensors with less thickness. The δemf values of the sensor are linearly increased up to 460oCoperating temperature and became stable above 460oC. Between 460-500oC temperatures regionthe sensor has reached an equilibrium state and the experimentally obtained δemf values areabout 80% of the theoretically calculated values. A Nernst’s slope of -61mV/decade has beenobtained between 250 to 5000 ppm of CO2 concentration at 500oC temperature. The sensor issuitable for ease of mass production in view of its miniaturization and cost effectiveness aftersome further improvement.

  7. Potentiometric Sensors Based on Surface Molecular Imprinting: Detection of Cancer Biomarkers and Viruses

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Y.; Zhang, Z; Jain, V; Yi, J; Mueller, S; Sokolov, J; Liu, Z; Levon, K; Rigas, B; Rafailovich, M

    2010-01-01

    The continuing discovery of cancer biomarkers necessitates improved methods for their detection. Molecular imprinting using artificial materials provides an alternative to the detection of a wide range of substances. We applied surface molecular imprinting using self-assembled monolayers to design sensing elements for the detection of cancer biomarkers and other proteins. These elements consist of a gold-coated silicon chip onto which hydroxyl-terminated alkanethiol molecules and template biomolecule are co-adsorbed, where the thiol molecules are chemically bound to the metal substrate and self-assembled into highly ordered monolayers, the biomolecules can be removed, creating the foot-print cavities in the monolayer matrix for this kind of template molecules. Re-adsorption of the biomolecules to the sensing chip changes its potential, which can be measured potentiometrically. We applied this method to the detection of carcinoembryonic antigen (CEA) in both solutions of purified CEA and in the culture medium of a CEA-producing human colon cancer cell line. The CEA assay, validated also against a standard immunoassay, was both sensitive (detection range 2.5-250 ng/mL) and specific (no cross-reactivity with hemoglobin; no response by a non-imprinted sensor). Similar results were obtained for human amylase. In addition, we detected virions of poliovirus in a specific manner (no cross-reactivity to adenovirus, no response by a non-imprinted sensor). Our findings demonstrate the application of the principles of molecular imprinting to the development of a new method for the detection of protein cancer biomarkers and to protein-based macromolecular structures such as the capsid of a virion. This approach has the potential of generating a general assay methodology that could be highly sensitive, specific, simple and likely inexpensive.

  8. The influence of Al, Mg, and Na on uranium analysis using potentiometric method

    International Nuclear Information System (INIS)

    The uranium concentration in uranyl nitrate solution from the dissolution of fuel element plate U3O8-Al has been analyzed using potentiometric method. The determination of uranium concentration is performed using redox method with ferro sulfate as the reductor and potassium bichromate as the oxidator. Uranyl nitrate solution obtained from the dissolution of fuel plate appears to contain impurities at relatively high concentration. To observe the influence of the impurities, sample preparation was performed employing heating with HClO4 and without heating. The results of uranium analysis in uranyl nitrate solution obtained from the dissolution of fuel elements plate with heating and without heating are 5.755 g/L and 5.105 g/L correspondingly. The difference in the analysis results is quite significant due to the presence of impurities Na, Mg and Al in the uranyl nitrate solution at rather high concentrations. The experiment results show that the influence of Al is noted at the concentrations of 8000 ppm and 10 000 ppm with accuracy of 95.06% and 87.09% respectively. The influence of Na is noted at the concentrations of 8000 ppm and 10 000 ppm with accuracy of 95.06% and 87.09%, respectively. The influence of Mg is noted at the concentration of 10 000 ppm with accuracy of 96.23%. The combined influence of the three elements commences at the concentrations of 1000 ppm, 2000 ppm, and 4000 ppm with accuracy of 94.37%, 94.97%, and 87.48% respectively. The combined influence at the concentration of 6000 ppm or higher cannot be measured. (author)

  9. Phenytoin speciation with potentiometric and chronopotentiometric ion-selective membrane electrodes.

    Science.gov (United States)

    Jansod, Sutida; Afshar, Majid Ghahraman; Crespo, Gastón A; Bakker, Eric

    2016-05-15

    We report on an electrochemical protocol based on perm-selective membranes to provide valuable information about the speciation of ionizable drugs, with phenytoin as a model example. Membranes containing varying amounts of tetradodecylammonium chloride (TDDA) were read out at zero current (potentiometry) and with applied current techniques (chronopotentiometry). Potentiometry allows one to assess the ionized form of phenytoin (pKa~8.2) that corresponds to a negatively monocharged ion. A careful optimization of the membrane components resulted in a lower limit of detection (~1.6 µM) than previous reports. Once the pH (from 9 to 10) or the concentration of albumin is varied in the sample (from 0 to 30 g L(-1)), the potentiometric signal changes abruptly as a result of reducing/increasing the ionized concentration of phenytoin. Therefore, potentiometry as a single technique is by itself not sufficient to obtain information about the concentration and speciation of the drug in the system. For this reason, a tandem configuration with chronopotentiometry as additional readout principle was used to determine the total and ionized concentration of phenytoin. In samples containing excess albumin the rate-limiting step for the chronopotentiometry readout appears to be the diffusion of ionized phenytoin preceded by comparatively rapid deprotonation and decomplexation reactions. This protocol was applied to measure phenytoin in pharmaceutical tables (100mg per tablet). This tandem approach can likely be extended to more ionizable drugs and may eventually be utilized in view of pharmacological monitoring of drugs during the delivery process. PMID:26703989

  10. Computational prediction and experimental selectivity coefficients for hydroxyzine and cetirizine molecularly imprinted polymer based potentiometric sensors

    International Nuclear Information System (INIS)

    Graphical abstract: -- Highlights: •Possible configurations template/monomer complexes were designed and optimized. •Effect of the electrostatic force on the selectivity of MIPs was investigated. •A correlation between selectivity of sensors and a charge distribution was obtained. -- Abstract: In spite of the increasing usages number of molecularly imprinted polymers (MIPs) in many scientific applications, the theoretical aspects of participating intra molecular forces are not fully understood. This work investigates effects of the electrostatic force, the Mulliken charge and the role of cavity's backbone atoms on the selectivity of MIPs. Moreover, charge distribution, which is a computational parameter, was proposed for the prediction of the selectivity coefficients of MIP-based sensors. In the computational approaches and experimental study, methacrylic acid (MAA) was chosen as the functional monomer and ethylene glycol dimethacrylate (EGDMA) as the cross linker for hydroxyzine and cetirizine imprinted polymers. Ab initio, DFT B3LYP method was carried out on molecular optimization. With regard to results obtained from molecules optimization and hydrogen bonding properties, possible configurations of 1:n (n ≤ 5) template/monomer complexes were designed and optimized. The binding energy for each complex in gas phase was calculated. Depending on the most stable configuration, hydroxyzine and cetirizine imprinted polymer models were designed. The calculations including the porogen were also investigated. The theoretical charge distributions for the template and some potential interfering molecules were calculated. The results showed a correlation between the selectivity coefficients and the theoretical charge distributions. The results surprisingly show that charge distribution based model was able to predict the selectivity coefficients of MIP based potentiometric sensors

  11. Potentiometric Sensor for Real-Time Monitoring of Multivalent Ion Concentrations in Molten Salt

    Energy Technology Data Exchange (ETDEWEB)

    Peter A. Zink; Jan-Fong Jue; Brenda E. Serrano; Guy L. Fredrickson; Ben F. Cowan; Steven D. Herrmann; Shelly X. Li

    2010-07-01

    Electrorefining of spent metallic nuclear fuel in high temperature molten salt systems is a core technology in pyroprocessing, which in turn plays a critical role in the development of advanced fuel cycle technologies. In electrorefining, spent nuclear fuel is treated electrochemically in order to effect separations between uranium, noble metals, and active metals, which include the transuranics. The accumulation of active metals in a lithium chloride-potassium chloride (LiCl-KCl) eutectic molten salt electrolyte occurs at the expense of the UCl3-oxidant concentration in the electrolyte, which must be periodically replenished. Our interests lie with the accumulation of active metals in the molten salt electrolyte. The real-time monitoring of actinide concentrations in the molten salt electrolyte is highly desirable for controlling electrochemical operations and assuring materials control and accountancy. However, real-time monitoring is not possible with current methods for sampling and chemical analysis. A new solid-state electrochemical sensor is being developed for real-time monitoring of actinide ion concentrations in a molten salt electrorefiner. The ultimate function of the sensor is to monitor plutonium concentrations during electrorefining operations, but in this work gadolinium was employed as a surrogate material for plutonium. In a parametric study, polycrystalline sodium beta double-prime alumina (Na-ß?-alumina) discs and tubes were subject to vapor-phase exchange with gadolinium ions (Gd3+) using a gadolinium chloride salt (GdCl3) as a precursor to produce gadolinium beta double-prime alumina (Gd-ß?-alumina) samples. Electrochemical impedance spectroscopy and microstructural analysis were performed on the ion-exchanged discs to determine the relationship between ion exchange and Gd3+ ion conductivity. The ion-exchanged tubes were configured as potentiometric sensors in order to monitor real-time Gd3+ ion concentrations in mixtures of gadolinium

  12. A Geochemical Reaction Model for Titration of Contaminated Soil and Groundwater at the Oak Ridge Reservation

    Science.gov (United States)

    Zhang, F.; Parker, J. C.; Gu, B.; Luo, W.; Brooks, S. C.; Spalding, B. P.; Jardine, P. M.; Watson, D. B.

    2007-12-01

    This study investigates geochemical reactions during titration of contaminated soil and groundwater at the Oak Ridge Reservation in eastern Tennessee. The soils and groundwater exhibits low pH and high concentrations of aluminum, calcium, magnesium, manganese, various trace metals such as nickel and cobalt, and radionuclides such as uranium and technetium. The mobility of many of the contaminant species diminishes with increasing pH. However, base additions to increase pH are strongly buffered by various precipitation/dissolution and adsorption/desorption reactions. The ability to predict acid-base behavior and associated geochemical effects is thus critical to evaluate remediation performance of pH manipulation strategies. This study was undertaken to develop a practical but generally applicable geochemical model to predict aqueous and solid-phase speciation during soil and groundwater titration. To model titration in the presence of aquifer solids, an approach proposed by Spalding and Spalding (2001) was utilized, which treats aquifer solids as a polyprotic acid. Previous studies have shown that Fe and Al-oxyhydroxides strongly sorb dissolved Ni, U and Tc species. In this study, since the total Fe concentration is much smaller than that of Al, only ion exchange reactions associated with Al hydroxides are considered. An equilibrium reaction model that includes aqueous complexation, precipitation, ion exchange, and soil buffering reactions was developed and implemented in the code HydroGeoChem 5.0 (HGC5). Comparison of model results with experimental titration curves for contaminated groundwater alone and for soil- water systems indicated close agreement. This study is expected to facilitate field-scale modeling of geochemical processes under conditions with highly variable pH to develop practical methods to control contaminant mobility at geochemically complex sites.

  13. Importance of anticomplement immunofluorescence antibody titration for diagnosing varicella-zoster virus infection in Bell's palsy.

    OpenAIRE

    Shigeta, S; Baba, M.; Ogata, M.; Nozaki, H.; Okuaki, A; Nakamura, S

    1986-01-01

    Anticomplement Immunofluorescence was used for antibody titration against varicella-zoster virus (VZV) in 43 patients with peripheral facial palsy. Nine of 31 patients (29%) with Bell's palsy and eight of 12 patients (75%) with Ramsey-Hunt syndrome had anticomplement immunofluorescence antibody titres of greater than or equal to 1/10. On the other hand, none of 14 patients with herpes simplex virus (HSV) infection and 51 healthy adults showed anticomplement immunofluorescence antibody titres ...

  14. The coulometric titration of acids and bases in m-cresol medium

    NARCIS (Netherlands)

    Bos, M.; Dahmen, E.A.M.F.

    1974-01-01

    A method is described for the coulometric titration of acids and bases in the solvent m-cresol. The method is suitable for bases with pKa values greater than 11 in m-cresol, or for acids with pKa values below 13 in m-cresol. Amounts of 5–50 μeq of acid or base can be determined with a relative accur

  15. Quantitative determination of acidic groups in functionalized graphene by direct titration

    Czech Academy of Sciences Publication Activity Database

    Ederer, J.; Janoš, P.; Ecorchard, Petra; Štengl, Václav; Bělčická, Zuzana; Šťastný, Martin; Pop-Georgievski, Ognen; Dohnal, V.

    2016-01-01

    Roč. 103, JUN (2016), s. 44-53. ISSN 1381-5148 R&D Projects: GA ČR(CZ) GA14-05146S Institutional support: RVO:61388980 ; RVO:61389013 Keywords : Acid-base titration * Carboxylic functional groups * Graphene oxide * Phenolic functional groups * Proton-binding model Subject RIV: CA - Inorganic Chemistry; CD - Macromolecular Chemistry (UMCH-V) Impact factor: 2.515, year: 2014

  16. Key considerations in the determination of polyelectrolyte concentration by the colloidal titration method

    OpenAIRE

    Miguel A. Zanuttini; Paulina Mocchiutti

    2007-01-01

    Medium or high charge density cationic polyelectrolytes are frequently used for water treatment. In the papermaking wet-end they are used as retention agents or as flocculating aids. Negative polyelectrolytes that enter the papermaking system increase the demand for cationic poly-electrolytes. Polyelectrolyte concentration can be determined by the colloidal titration method, using either of two options for detecting the endpoint: i) visual observation or spectrophotometric determination of th...

  17. Measurement of VFA in anaerobic digestion: The five-point titration method revisited

    OpenAIRE

    Lahav, O.; Loewenthal, R. E.

    2000-01-01

    The 5-point titration method proposed by Moosbrugger et al. (1993)provides a cheap and rapid means form measuring inter alia short chain volatile fatty acids. However, output from the analysis requires invoking a 'systematic pH error'. The authors ascribed this to either residual liquid junction potential effects ol pH calibration errors. However, from a scientific standpoint this detracts from confidence in the method. In this paper, it is shown that Moosbrugger et al's 'systematic pH error'...

  18. DETERMINATION OF NITRATE NITROGEN IN SURFACE WATER: COMPARISON OF DISTILATION-TITRATION AND SPECTROPHOTOMETRIC METHODS

    OpenAIRE

    JAKUB ELBL; KATEŘINA ZÁKOUTSKÁ; JAROSLAV ZÁHORA; PETRA OPELTOVÁ; ANTONÍN KINTL; LUKÁŠ PLOŠEK

    2014-01-01

    This work deals with comparison of two methods for determination of mineral nitrogen in surface water. The distillation-titration and spectrophotometric methods were compared. From January to September 2013, mineral nitrogen was determined by both methods in samples, which were taken from seven sites. These sites are located in CHKO Jizera Mountains. Water sampling was carried out every month (from April to August 2013). Based on the statistical analysis of results from each...

  19. Monitoring of an RNA Multistep Folding Pathway by Isothermal Titration Calorimetry

    OpenAIRE

    Reymond, Cédric; Bisaillon, Martin; Perreault, Jean-Pierre

    2008-01-01

    Isothermal titration calorimetry was used to monitor the energetic landscape of a catalytic RNA, specifically that of the hepatitis delta virus ribozyme. Using mutants that isolated various tertiary interactions, the thermodynamic parameters of several ribozyme-substrate intermediates were determined. The results shed light on the impact of several tertiary interactions on the global structure of the ribozyme. In addition, the data indicate that the formation of the P1.1 pseudoknot is the lim...

  20. Heats of Mixing Using an Isothermal Titration Calorimeter: Associated Thermal Effects

    OpenAIRE

    Fabiola Socorro; Manuel Rodríguez de Rivera; Matos, José S.

    2009-01-01

    The correct determination of the energy generated or absorbed in the sample cell of an Isothermal Titration Calorimeter (ITC) requires a thorough analysis of the calorimetric signal. This means the identification and quantification of any thermal effect inherent to the working method. In this work, it is carried out a review on several thermal effects, studied by us in previous work, and which appear when an ITC is used for measuring the heats of mixing of liquids in a continuous mode. These ...