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Sample records for boric acid samples

  1. Determination of uranium in boric acid samples at Paks Nuclear Power Plant by ICP-MS method

    International Nuclear Information System (INIS)

    Komlosi, E.Zs.; Menyhart, A.; Varju, I.

    2005-01-01

    Measurement of uranium became necessary in 2003, after the incident of unit 2 in April, when the fission products, uranium and transuranium isotopes got into the cooling water. The measurement of uranium with ICP-MS method was initiated in January 2004. Apparatus type Agilent 7500a was used. Uranium concentration and uranium isotope ratio were measured in samples with different - but known - boric acid concentration. Internal standard was used for the elimination of the matrix effect. The samples have high boric acid concentration (in few samples over 20 g/litres). Two methods were used for the reduction of the boric acid concentration: dilution and evaporation with ethyl alcohol. Both methods were found successful and exact. The limit of detection is 0.1 ng/litres for the Uranium-238. (N.T.)

  2. Spectrophotometric determination of boric acid in boron powder with curcumin

    International Nuclear Information System (INIS)

    Grotheer, E.W.

    1979-01-01

    A rapid and accurate method was needed to determine trace amounts of boric acid for quality control and specification testing of elemental boron. The reaction between boric acid and curcumin occurs at a measurable rate only when the curcumin molecule is protonated. Protonation takes place at the carbonyl groups in the presence of a strong acid and occurs completely and rapidly when sulfuric acid is added to a solution of curcumin in acetic acid. Spectrophotometric measurements were made. The extraction of boric acid from boron powder was found to be complete within 2h when either water or the diol solution was used. Whatman No. 40 cr 42 filter paper was used to obtain diol samples free of boron particles. The extraction efficiency of 2-ethyl-1,3-hexanediol was evaluated by adding 1 ml of 500 ppM aqueous boric acid and 1 drop of 10% NaOH to accurately weighed samples of boron powder. The water then was evaporated at room temperature and the samples were extracted with diol solution. The data obtained are included. The extraction efficiency also was evaluated by determining the boric acid content of boron which had been recovered from a previous extraction and boric acid determination. The determination of boric acid using curcumin is unaffected by the presence of other compounds, except for fluoride and nitrate ions. 2 tables

  3. Chemical Reaction between Boric Acid and Phosphine Indicates Boric Acid as an Antidote for Aluminium Phosphide Poisoning

    Directory of Open Access Journals (Sweden)

    Motahareh Soltani

    2016-08-01

    Full Text Available Objectives: Aluminium phosphide (AlP is a fumigant pesticide which protects stored grains from insects and rodents. When it comes into contact with moisture, AlP releases phosphine (PH3, a highly toxic gas. No efficient antidote has been found for AlP poisoning so far and most people who are poisoned do not survive. Boric acid is a Lewis acid with an empty p orbital which accepts electrons. This study aimed to investigate the neutralisation of PH3 gas with boric acid. Methods: This study was carried out at the Baharlou Hospital, Tehran University of Medical Sciences, Tehran, Iran, between December 2013 and February 2014. The volume of released gas, rate of gas evolution and changes in pH were measured during reactions of AlP tablets with water, acidified water, saturated boric acid solution, acidified saturated boric acid solution, activated charcoal and acidified activated charcoal. Infrared spectroscopy was used to study the resulting probable adduct between PH3 and boric acid. Results: Activated charcoal significantly reduced the volume of released gas (P <0.01. Although boric acid did not significantly reduce the volume of released gas, it significantly reduced the rate of gas evolution (P <0.01. A gaseous adduct was formed in the reaction between pure AlP and boric acid. Conclusion: These findings indicate that boric acid may be an efficient and non-toxic antidote for PH3 poisoning.

  4. Recovery of boric acid from ion exchangers

    International Nuclear Information System (INIS)

    Pollock, C.W.

    1976-01-01

    The recovery of boric acid from an anion exchange resin is improved by eluting the boric acid with an aqueous solution of ammonium bicarbonate. The boric acid can be readily purified and concentrated by distilling off the water and ammonium bicarbonate. This process is especially useful for the recovery of boric acid containing a high percentage of 10 B which may be found in some nuclear reactor coolant solutions. 10 claims

  5. LITERATURE REVIEW OF BORIC ACID SOLUBILITY DATA

    Energy Technology Data Exchange (ETDEWEB)

    Crapse, K.; Kyser, E.

    2011-09-22

    A new solvent system is being evaluated for use in the Modular Caustic-Side Solvent Extraction Unit (MCU) and in the Salt Waste Processing Facility (SWPF). The new system replaces the current dilute nitric acid strip solution with 0.01 M boric acid. This literature study is performed to determine if there is a potential for boric acid to crystallize in the lines with emphasis on the transfer lines to the Defense Waste Processing Facility. This report focuses on the aqueous phase chemistry of boric acid under conditions relevant to MCU and SWPF. Operating and transfer conditions examined for the purpose of this review include temperatures between 13 C (McLeskey, 2008) and 45 C (Fondeur, 2007) and concentrations from 0 to 3M in nitric acid as well as exposure of small amounts of entrained boric acid in the organic phase to the sodium hydroxide caustic wash stream. Experiments were also conducted to observe any chemical reactions and off-gas generation that could occur when 0.01 M boric acid solution mixes with 3 M nitric acid solution and vice versa. Based on the low concentration (0.01M) of boric acid in the MCU/SWPF strip acid and the moderate operating temperatures (13 C to 45 C), it is unlikely that crystallization of boric acid will occur in the acid strip solution under process or transfer conditions. Mixing experiments of boric and nitric acid show no measurable gas generation (< 1 cc of gas per liter of solution) under similar process conditions.

  6. The development of precisely analytical method for the concentrated boric acid solution in the NPP systems

    Energy Technology Data Exchange (ETDEWEB)

    Sung, G. B.; Jung, K. H.; Kang, D. W. [KEPRI, Taejon (Korea, Republic of); Park, C. S. [KEPCO, Taejon (Korea, Republic of)

    1999-05-01

    Boric acid is used for reactivity control in nuclear reactors, which frequently results in leftover boric acid. This extra boric acid is stored in boric acid storage tank after the concentration process by boric acid evaporator. Apart from this excess, highly concentrated boric acid is stored in safety-related boric acid storage tank. Accordingly, proper maintenance of these boric acid is one of the greatest safety concerns. The solubility of boric acid decreases with decreasing temperature resulting in its precipitation. Consequently, the temperature of boric acid storage tanks is maintained at high temperature. The following analysis should be also performed at the similar temperature to prevent the formation of boric acid precipitation, which is difficult to achieve affecting the accuracy of analytical results. This paper presents a new sampling and measuring technique that makes up for the difficulties mentioned above and shows several advantages including improved reliability and short analysis time. This method is based on gravimetry and dilution method and is expected to be widely used in field application.

  7. Recovery of boric acid from nuclear waste

    International Nuclear Information System (INIS)

    Lahoda, E.J.

    1985-01-01

    Disclosed is a process for separating and recovering boric acid from water containing solids which include boric acid and radionuclides. In the first step, the water is separated from the solids by evaporation of the water at a temperature under 130 0 F In the second step, an alcohol selected from the group consisting of methanol, ethanol, propanol, isopropanol, and mixtures thereof is added to the remaining solids in the amount of at least 1.4 times that stoichiometrically required to react with the boric acid to form boron alkoxide and water to about 100 mole % in excess of stoichiometric. In the third step, the boron alkoxide is separated from the remaining solids by evaporation of the boron alkoxide. In the fourth step, water is added to the volatilized boron alkoxide to form boric acid and an alcohol. And finally, the alcohol is separated from the boric acid by evaporating the alcohol

  8. Processing of nuclear power plant waste streams containing boric acid

    International Nuclear Information System (INIS)

    1996-10-01

    Boric acid is used in PWR type reactor's primary coolant circuit to control the neutron flux. However, boric acid complicates the control of water chemistry of primary coolant and the liquid radioactive waste produced from NPP. The purpose of this report is to provide member states with up-to-date information and guidelines for the treatment and conditioning of boric acid containing wastes. It contains chapters on: (a) characteristics of waste streams; (b) options for management of boric acid containing waste; (c) treatment/decontamination of boric acid containing waste; (d) concentration and immobilization of boric acid containing waste; (e) recovery and re-use of boric acid; (f) selected industrial processes in various countries; and (g) the influence of economic factors on process selection. 72 refs, 23 figs, 5 tabs

  9. The Acid-Base Titration of a Very Weak Acid: Boric Acid

    Science.gov (United States)

    Celeste, M.; Azevedo, C.; Cavaleiro, Ana M. V.

    2012-01-01

    A laboratory experiment based on the titration of boric acid with strong base in the presence of d-mannitol is described. Boric acid is a very weak acid and direct titration with NaOH is not possible. An auxiliary reagent that contributes to the release of protons in a known stoichiometry facilitates the acid-base titration. Students obtain the…

  10. The role of boric acid in the Phebus-FP tests

    International Nuclear Information System (INIS)

    Bowsher, B.R.

    1991-12-01

    The data in this report should enable proposed methods for the introduction of boric acid into the Phebus-FP tests to be assessed. Boric acid chemistry is reviewed in the condensed, vapour and aqueous phases. The chemistry of concentrated aqueous solutions of boric acid is complex, involving polyborate species resulting in enhanced acidities. Equations are presented that allow the partition of boric acid between the vapour and aqueous phase to be calculated at different boric acid concentrations. The volatility of boric acid is enhanced significantly in the presence of steam. Equations are given that allow the effective vapour pressure of boric acid to be determined as functions of the water vapour pressure for temperatures in the range from 723 to 1000 o C. These data are confirmed by experimental studies designed to simulate specific aspects of the conditions in the Phebus-FP tests. (author)

  11. MCB-2 concentration meter for boric acid

    International Nuclear Information System (INIS)

    Lisecki, W.

    1978-01-01

    The principles are explained of the thermal neutron absorption method for monitoring boric acid concentration in the WWER type reactor coolant. The design principles and the characteristics of four variants are described of the MSB-2 type boric acid concentration monitor developed by IBJ. (B.S.)

  12. Effects of an inorganic insecticide (boric acid) against Blattella ...

    African Journals Online (AJOL)

    In order to obtain more information on the mode of action of boric acid, which has not been satisfactorily established, a biometric and biochemical study of the ovaries was done following the toxicity assays after having evaluated the toxicity of the boric acid against B. germanica. Boric acid was injected at two doses, 77.62 ...

  13. Solubilities of boric acid in heavy water

    International Nuclear Information System (INIS)

    Nakai, Shigetsugu; Aoi, Hideki; Hayashi, Ken-ichi; Katoh, Taizo; Watanabe, Takashi.

    1988-01-01

    A gravimetric analysis using meta-boric acid (HBO 2 or DBO 2 ) as a weighing form has been developed for solubility measurement. The method gave satisfactory results in preliminary measurement of solubilities of boric acid in light water. By using this method, the solubilities of 10 B enriched D 3 BO 3 in heavy water were measured. The results are as follows; 2.67 (7deg C), 3.52 (15deg C), 5.70 (30deg C), 8.87 (50deg C) and 12.92 (70deg C) w/o, respectively. These values are about 10% lower than those in light water. Thermodynamical consideration based on the data shows that boric acid is the water structure breaker. (author)

  14. Evaporation of boric acid from sea water

    Energy Technology Data Exchange (ETDEWEB)

    Gast, J A; Thompson, T G

    1959-01-01

    Previous investigators have shown that the boron-chlorinity ratios of rain waters are many times greater than the boron-chlorinity ratio of sea water. The presence of boron in the atmosphere has been attributed to sea spray, volcanic activity, accumulation in dust, evaporation from plants, and industrial pollution. In this paper data are presented to demonstrate that boric acid in sea water has a vapor pressure at ordinary temperatures of the sea and, when sea water evaporates, boric acid occurs in the condensate of the water vapor. It is postulated that, while some of the boron in the atmosphere can be attributed to the sources mentioned above, most of the boric acid results from evaporation from the sea.

  15. Aqueous Boric acid injection facility of PWR type reactor

    International Nuclear Information System (INIS)

    Matsuoka, Tsuyoshi; Iwami, Masao.

    1996-01-01

    If a rupture should be caused in a secondary system of a PWR type reactor, pressure of a primary coolant recycling system is lowered, and a back flow check valve is opened in response to the lowering of the pressure. Then, low temperature aqueous boric acid in the lower portion of a pressurized tank is flown into the primary coolant recycling system based on the pressure difference, and the aqueous boric acid reaches the reactor core together with coolants to suppress reactivity. If the injection is continued, high temperature aqueous boric acid in the upper portion boils under a reduced pressure, further urges the low temperature aqueous boric acid in the lower portion by the steam pressure and injects the same to the primary system. The aqueous boric acid stream from the pressurized tank flowing by self evaporation of the high temperature aqueous boric acid itself is rectified by a rectifying device to prevent occurrence of vortex flow, and the steam is injected in a state of uniform stream. When the pressure in the pressurized tank is lowered, a bypass valve is opened to introduce the high pressure fluid of primary system into the pressurized tank to keep the pressure to a predetermined value. When the pressure in the pressurized tank is elevated to higher than the pressure of the primary system, a back flow check valve is opened, and high pressure aqueous boric acid is flown out of the pressurized tank to keep the pressure to a predetermined value. (N.H.)

  16. Boric Acid Reclamation System (BARS)

    International Nuclear Information System (INIS)

    Kniazewycz, B.G.; Markind, J.

    1986-03-01

    KLM Technologies' personnel have identified a Boric Acid Reclamation System (BARS) utilizing reverse osmosis and ultrafiltration to produce a recyclable grade of otherwise waste boric acid at PWRs, thus reducing a major source of low-level radwaste. The design of a prototype BARS as a compact volume reduction system was the result of KLM's Phase 1 Program, and based upon a preliminary feasibility program, which assessed the applicability of membrane technology to refurbish and recycle waste boric acid from floor and equipment drain streams. The analysis of the overall program indicated a substantial savings regarding off-site disposal costs. Today's economic scenario indicates that optimization of volume reduction operation procedures could significantly reduce waste management costs, especially where burial penalties have become more severe. As a reaction to the economic burden imposed by final disposal, many nuclear plants are currently modifying their design and operating philosophies concerning liquid radwaste processing systems to meet stricter environmental regulations, and to derive potential economic benefits by reducing the ever-increasing volumes of wastes that are produced. To effect these changes, innovative practices in waste management and more efficient processing technologies are being successfully implemented

  17. Boric acid corrosion of low alloy steel

    Energy Technology Data Exchange (ETDEWEB)

    Jones, R.; White, G.; Collin, J.; Marks, C. [Dominion Engineering, Inc., Reston, Virginia (United States); Reid, R.; Crooker, P. [Electric Power Research Inst., Palo Alto, California (United States)

    2010-07-01

    In the last decade, the industry has been aware of a potential loss of coolant accident (LOCA) per the following scenario: primary water stress corrosion cracking (PWSCC) of a primary system component or weld leads to a coolant leak, the coolant corrodes a low alloy steel structural component (e.g., the reactor vessel (RV) or the reactor vessel head (RVH)), and corrosion degrades the pressure boundary leading to a loss of coolant accident. The industry has taken several steps to address this concern, including replacement of the most susceptible components (RVH replacement), enhanced inspection (both NDE of components and visual inspections for boric acid deposits), and safety analyses to determine appropriate inspection intervals. Although these measures are generally thought to have adequately addressed this issue, there have been some uncertainties in the safety analyses which the industry has sought to address in order to quantify the extent of conservatism in the safety analyses. Specifically, there has been some uncertainty regarding the rate of boric acid corrosion under various conditions which might arise due to a PWSCC leak and the extent to which boric acid deposits are retained near the leak under various geometries. This paper reviews the results of the Electric Power Research Institute (EPRI) Materials Reliability Program (MRP) boric acid corrosion (BAC) test programs conducted over the last 8 years, focusing on the most recent results of full-scale mockup testing of CRDM nozzle and bottom mounted nozzle (BMN) configurations. The main purpose of this presentation is to provide an overview of the latest understanding of the risk of boric acid corrosion as it is informed by the results of the testing conducted over the last eight years. The rate of boric acid corrosion has been found to be a function of many factors, including initial chemistry, the extent of concentration due to boiling, the temperature at which concentration takes place, the velocity

  18. General corrosion of metallic materials in boric acid environments

    International Nuclear Information System (INIS)

    Gras, J.M.

    1994-05-01

    Certain low-alloy steel components in PWR primary circuit were corroded by leaking water containing boric acid. A number of studies have been performed by manufacturers in the USA and by EDF in France to determine the rate of general corrosion for low-alloy steels in media containing varying concentrations of boric acid. The first part of this paper summarizes the studies performed and indicates how far work has advanced to date in establishing the resistance of stainless steels to general corrosion in concentrated boric acid solutions. The second part of the paper discusses the mechanism of corrosion and proposes a model. Carbon steels and low-alloy steels - carbon steels and low-alloy steels in deaerated diluted boric acid solutions (pH > 4) corrode very slowly ( -1 . (author). 31 refs., 12 figs., 13 tabs

  19. Ion exchange separation of low boric acid concentrations from water

    International Nuclear Information System (INIS)

    Kysela, J.; Brabec, J.; Peterka, F.

    1975-01-01

    Boric acid poisoning of the moderator of the TR-O experimental heavy water reactor was studied. The possibility is discussed of removing boric acid from heavy water by means of a strong basic anion exchanger, below the residual concentration of 0.01 mg B/l. Measurements of the usable capacities of the strong basic anion exchanger Zerollit FF showed that the penetration of boric acid during the sorption period does not exceed the value of 0.015 mg B/l. The dependence was found of capacity on the boric acid concentration in the solution. Analytical methods used to determine B in water are also described. (author)

  20. Boric Acid Reclamation System (BARS)

    International Nuclear Information System (INIS)

    Kniazewycz, B.G.; Markind, J.

    1986-01-01

    KLM Technologies was recently awarded a contract by the Department of Energy for a Phase II demonstration of an optimized full-scale prototype membrane system including performance evaluation under plant operating conditions. The program will serve as the catalyst for developing technology to augment the industry's incentive toward innovative and compact volume reduction alternatives for PWRs. The development and demonstration of the KLM Boric Acid Reclamation System, which is readily retrofitted into existing PWR facilities, will provide a positive means of reducing PWR waste volumes without requiring the $25-50 million equipment and support facility expenditures associated with most liquid waste volume reduction systems. This new application for membrane separation technology can reduce waste by upward of 50 percent for two-thirds of the operating nuclear plants in the U.S. The use of membrane technology has demonstrated significant process potential in radwaste and related applications. Reverse Osmosis (RO) and Ultrafiltration (UF) can provide selective filtration capability and concentrate contaminants without the need of filter aids, thus minimizing the requirements of chemical regeneration, costly resins, and major process equipment with large auxiliary heat supplies. KLM Technologies' personnel have identified a Boric Acid Reclamation System (BARS) utilizing RO and UF to produce a recyclable grade of otherwise waste boric acid at PWRs, thus reducing a major source of low-level radwaste. The design of a prototype BARS as a compact volume reduction system was the result of KLM's Phase I Program, and based upon a preliminary feasibility program, which assessed the applicability of membrane technology to refurbish and recycle waste boric acid from floor and equipment drain streams. The analysis of the overall program indicated a substantial savings regarding off-site disposal costs

  1. Study of boric acid sorption and desorption processes

    International Nuclear Information System (INIS)

    Czosnowska, B.; Laren, E.

    1978-01-01

    The results are given of the experimental determination of the effect on the boric acid flow and sorption and desorption efficiency of the flow rate of boric acid at different concentrations through an ion exchange column 10.2 cm 2 in cross section. The strongly alkaline VOFATIT RO ion exchanger was used. (B.S.)

  2. Characterisation of boric acid aerosol behaviour and interactions with stainless steel

    International Nuclear Information System (INIS)

    Anderson, A.B.; Beard, A.M.; Bennett, P.J.; Benson, C.G.

    1991-03-01

    Experiments have been conducted to determine the physical characteristics of boric acid aerosol. Aqueous solutions of boric acid (either 200 or 2000 ppm boron) were injected at a controlled rate onto a 304 stainless steel cone held at 1000 o C. The transport and deposition of the resulting aerosol was studied through a system including pipework and a dilution chamber. Work was also undertaken to characterise the interaction between boric acid and stainless steel. Boric acid was vaporized in steam-argon atmospheres at 300 o C and passed over 304 stainless steel coupons held at temperatures between 400 and 1000 o C. (author)

  3. Effect of boric acid on intergranular corrosion in tube support plate crevices

    International Nuclear Information System (INIS)

    Brunet, J.P.; Campan, J.L.

    1993-10-01

    Intergranular attack on steam generator tubing is one important phenomenon involved in availability of Pressurized Water Reactors. Boric acid appears to be a possible candidate for inhibiting the corrosion process. The program performed in Cadarache was supposed to give statistical informations on the boric acid effect. It was based on a large number of samples initially attacked during a program performed by BABCOCK ampersand WILCOX. These samples were sleeved onto Alloy 690 tubes, in order to prevent premature cracking. Unfortunately it was not possible to find chemical conditions able to produce significant additional corrosion; we postulated mainly due to a drastic reduction of the thermal flux resulting from the increase of the tube wall thickness under the tube support plates (TSP). The tests demonstrate that such sleeve could be a possible remedy of the corrosion when introduced under the TSP. The tests show indications of a possible beneficial effect of the boric acid, a large variability of the heats sensitivity to the IGA and a predominant effect of Na 2 CO 3 on IGA production

  4. Boric acid solubility in the presence of alkali metal nitrides

    Energy Technology Data Exchange (ETDEWEB)

    Skvortsov, V G; Tsekhanskij, R S; Molodkin, A K; Sadetdinov, Sh V [Chuvashskij Gosudarstvennyj Univ., Cheboksary (USSR); Universitet Druzhby Narodov, Moscow (USSR))

    1983-01-01

    Methods of solubility and refractometry at 25 deg C have been applied to state that systems boric acid-lithium (sodium, potassium) nitrite-water are simple eutonic type systems. Nitrites salt in the acid and their lyotropic effect increases from lithium salt to potassium salt. The disclosed succession in change of the effect is determined by the character of cation hydration in the medium the acidic reaction of which is conditioned by boric acid polymerization and partial oxidation of nitrite ion into nitrate ion. Boric acid is salted out from solutions containing lithium and sodium cations with increase of nitrate ion.

  5. Boric acid solubility in the presence of alkali metal nitrides

    International Nuclear Information System (INIS)

    Skvortsov, V.G.; Tsekhanskij, R.S.; Molodkin, A.K.; Sadetdinov, Sh.V.

    1983-01-01

    Methods of solubility and refractometry at 25 deg C have been applied to state that systems boric acid-lithium (sodiUm, potassium) nitrite-water are simple eutonic type systems. Nitrites salt in the acid and their lyotropic effect increases from lithium salt to potassium salt. The disclosed succession in change of the effect is determined by the character of cation hydration in the medium the acidic reaction of which is conditioned by boric acid polymerization and partial oxidation of nitrite ion into nitrate ion Boric acid is salted out form solutions containing lithium and sodium cations with increase of nitrate ion

  6. Lubrication from mixture of boric acid with oils and greases

    Science.gov (United States)

    Erdemir, Ali

    1995-01-01

    Lubricating compositions including crystalline boric acid and a base lubricant selected from oils, greases and the like. The lubricity of conventional oils and greases can also be improved by adding concentrates of boric acid.

  7. High production of D-tagatose by the addition of boric acid.

    Science.gov (United States)

    Lim, Byung-Chul; Kim, Hye-Jung; Oh, Deok-Kun

    2007-01-01

    An L-arabinose isomerase mutant enzyme from Geobacillus thermodenitrificans was used to catalyze the isomerization of D-galactose to D-tagatose with boric acid. Maximum production of D-tagatose occurred at pH 8.5-9.0, 60 degrees C, and 0.4 molar ratio of boric acid to D-galactose, and the production increased with increasing enzyme concentration. Under the optimum conditions, the enzyme (10.8 units/mL) converted 300 g/L D-galactose to 230 g/L D-tagatose for 20 h with a yield of 77% (w/w); the production and conversion yield with boric acid were 1.5-fold and 24% higher than without boric acid, respectively. In 24 h, the enzyme produced 370 g/L D-tagatose from 500 g/L D-galactose with boric acid, corresponding to a conversion yield of 74% (w/w) and a production rate of 15.4 g/L.h. The production and yield of D-tagatose obtained in this study are unprecedented.

  8. Boric acid reduces axonal and myelin damage in experimental sciatic nerve injury

    Directory of Open Access Journals (Sweden)

    Zahir Kizilay

    2016-01-01

    Full Text Available The aim of this study was to investigate the effects of boric acid in experimental acute sciatic nerve injury. Twenty-eight adult male rats were randomly divided into four equal groups (n = 7: control (C, boric acid (BA, sciatic nerve injury (I , and sciatic nerve injury + boric acid treatment (BAI. Sciatic nerve injury was generated using a Yasargil aneurysm clip in the groups I and BAI. Boric acid was given four times at 100 mg/kg to rats in the groups BA and BAI after injury (by gavage at 0, 24, 48 and 72 hours but no injury was made in the group BA. In vivo electrophysiological tests were performed at the end of the day 4 and sciatic nerve tissue samples were taken for histopathological examination. The amplitude of compound action potential, the nerve conduction velocity and the number of axons were significantly lower and the myelin structure was found to be broken in group I compared with those in groups C and BA. However, the amplitude of the compound action potential, the nerve conduction velocity and the number of axons were significantly greater in group BAI than in group I. Moreover, myelin injury was significantly milder and the intensity of nuclear factor kappa B immunostaining was significantly weaker in group BAI than in group I. The results of this study show that administration of boric acid at 100 mg/kg after sciatic nerve injury in rats markedly reduces myelin and axonal injury and improves the electrophysiological function of injured sciatic nerve possibly through alleviating oxidative stress reactions.

  9. Effect of boric acid on intergranular corrosion and on hideout return efficiency of sodium in the tube support plate crevices

    International Nuclear Information System (INIS)

    Paine, J.P.N.; Shoemaker, C.E.; Campan, J.L.; Brunet, J.P.; Schindler, P.; Stutzmann, A.

    1995-01-01

    Sodium hydroxide is one of the main causes of intergranular attack/stress corrosion cracking (IGA/SCC) of alloy 600 steam generator (S.G.) tubes. Boric acid appears to be one of the possible remedies for intergranular corrosion process inhibition. In order to obtain data on boric acid injection efficiency, an experimental program was performed on previously corroded tubes. To prevent premature tube wall cracking, samples were sleeved on alloy 690 tubes. The objective of the tests was to evaluate, on a statistically valid number of samples, the effectiveness of boric acid and tube sleeving as possible remedies for IGA/SCC extension. Another independent experimental program was initiated to determine the hideout return efficiency in the tube support plate (TSP) and tubesheet (TS) crevices after a significant duration (≤ 180 hours) of sodium hideout. The main objective of the first tests being a statistical evaluation of the efficiency of boric acid treatment, was not achieved. The tests did demonstrate that sleeving effectively reduces IGA/SCC growth. In an additional program, cracks were obtained on highly susceptible tubes when specimens were not sleeved. The companion tests performed in the same conditions but with an addition of boric acid did not show any IGA or cracks. These results seem to demonstrate the possible effect of boric acid in preventing the corrosion process. Results of the second tests did not demonstrate any difference in the amount of sodium piled up in the crevices before and after boric acid injection. They however showed an increase of the hideout return efficiency at the tube support plate level from 78 % without boric acid to 95 % when boric acid is present in the feed water

  10. 40 CFR 721.3032 - Boric acid (H3BO2), zinc salt.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Boric acid (H3BO2), zinc salt. 721... Substances § 721.3032 Boric acid (H3BO2), zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO2), zinc salt (PMN P-97-553...

  11. Experimental Study and Reactive Transport Modeling of Boric Acid Leaching of Concrete

    Directory of Open Access Journals (Sweden)

    Chiang K.-T. K.

    2013-07-01

    Full Text Available Borated water leakage through spent fuel pools (SFPs at pressurized water reactors is a concern because it could cause corrosion of reinforcement steel in the concrete structure, compromise the integrity of the structure, or cause unmonitored releases of contaminated water to the environment. Experimental data indicate that pH is a critical parameter that determines the corrosion susceptibility of rebar in borated water and the degree of concrete degradation by boric acid leaching. In this study, reactive transport modeling of concrete leaching by borated water was performed to provide information on the solution pH in the concrete crack or matrix and the degree of concrete degradation at different locations of an SFP concrete structure exposed to borated water. Simulations up to 100 years were performed using different boric acid concentrations, crack apertures, and solution flow rates. Concrete cylinders were immersed in boric acid solutions for several months and the mineralogical changes and boric acid penetration in the concrete cylinder were evaluated as a function of time. The depths of concrete leaching by boric acid solution derived from the reactive transport simulations were compared with the measured boric acid penetration depth.

  12. Determination of contaminants in boric acid used as neutron moderator by means of ion chromatography and selective electrodes

    International Nuclear Information System (INIS)

    Pires, M.A.F.; Abrao, A.

    1988-07-01

    The boric acid used as neutron moderator in reactors must observe restrictions about the concentration of some impurities. According to Westinghouse (1) specification, the highest limits for sodium, sulphate, phosphate, fluoride, and chlorine are: Na + - 0,003%; SO 4 -2 - 0,0006%; PO 4 -3 - 0,003%; F - - 0,00002%; Cl - - 0,00004%. This paper describes the determination of ions above mentioned directly in the boric acid solution. The sample is dissolved in water or in an appropriate eluent and is injected in the ion chromatograph. Na + and F - are determined by means of selective electrodes. The determination limits found for F - (0,0002%) and Cl - (0,0002%) are not sufficiently low to attent the specifications. The determination limits found for SO 4 -2 (0,0005%), PO 4 -3 (0,0003%) and Na + (0,0005%) are good enough for nuclear pure boric acid analysis. In some samples nitrate (detection limit 0,0015%) was found as well. Boric acid from different suppliers were analysed. (author) [pt

  13. Liquid Superlubricity of Polyethylene Glycol Aqueous Solution Achieved with Boric Acid Additive.

    Science.gov (United States)

    Ge, Xiangyu; Li, Jinjin; Zhang, Chenhui; Luo, Jianbin

    2018-03-27

    Boric acid is a weak acid and has been used as a lubrication additive because of its special structure. In this study, we report that boric acid could achieve a robust superlubricity (μ friction coefficient of approximately 0.004-0.006 could be achieved with boric acid under neutral conditions (pH of approximately 6.4), which is different from the acidic conditions leading to superlubricity. The influence of various factors, including boric acid concentration, sliding speed, applied load, PEG molecular weight, and the volume of lubricant on the superlubricity, were investigated. The results reveal that the PEG aqueous solution with the boric acid additive could achieve superlubricity under a wide range of conditions. The surface composition analysis shows that the synergy effect between boric acid and PEG provides sufficient H + ions to realize the running-in process. Moreover, a composite tribochemical film composed of silica and ammonia-containing compounds were formed on the ball surface, contributing to the superlubricity. The film thickness calculation shows that superlubricity was achieved in a mixed lubrication region, and therefore, the superlubricity state was dominated by both the composite tribochemical film formed via the tribochemical reaction on the contact surfaces and the hydrodynamic lubricating film between the contact surfaces. Such a liquid superlubricity achieved under neutral conditions is of importance for both scientific understanding and engineering applications.

  14. KLM's Boric Acid Reclamation System (BARS): An update

    International Nuclear Information System (INIS)

    Schuelke, D.; Kniazewycz, B.G.; Markind, J.; Brossart, M.A.; Choi, R.C.

    1987-02-01

    KLM Technologies has implemented its Department of Energy Phase II Small Business Innovative Research (SBIR) demonstration program for a radioactive waste Boric Acid Reclamation System (BARS). Preliminary performance indicates enhanced treatment by the BARS technique over state of the art process methods for selective removal of silica and other impurities from borated water matrices. At optimal system recovery of 96 to 97%, BARS removes nominal levels of boric acid while achieving significant rejection for soluble silica and selective radioisotopes. This is indicative of superior performance compared to existing data governing standard boric acid process treatment in the presence of silica and other contaminants. Conventional technologies have also proven to be relatively expensive, utilizing costly chemically treated disposable resins for primary waste removal. The overall BARS program indicates substantial savings regarding off-site disposal costs based on reduced waste generation. Optimization of the BARS technology could have potential impact on conventional process technologies that are essentially non-selective in removal capacities. 2 figs

  15. Experimental and modeling study of Portland cement paste degradation in boric acid

    International Nuclear Information System (INIS)

    Benakli, A.; Chomat, L.; Le Bescop, P.; Wall, J.

    2015-01-01

    In the framework of Spent Fuel Pools (SFP) lifetime studies, an investigation of the Portland cement degradation in boric acid has been requested by the Electric Power Research Institute. The main goal of this study is to identify the physico-chemical degradation mechanisms involved in boric acid media. Both experimental and modeling approaches are considered. Concerning degradation experiments, sample of cement paste are immersed during three and nine months in a boric acid solution at 2400 ppm that is periodically renewed. Boric acid concentration has been chosen to be representative of SFP solution. Results will be confronted with reactive transport numerical calculations performed by the reactive transport code HYTEC associated with a dedicated extended database called Thermoddem. The analysis of degradation solution revealed a main ions release mechanism driven by diffusion especially for calcium, nitrate, sodium and sulfate. Leaching behavior of magnesium seems to be more complex. Decalcification is the major degradation process involved, even if a non-negligible contribution of further cations (Mg 2+ , Na + ) and anions (SO 4 2- ) has been noticed. Analysis of degradation soution also revealed that kinetic of Portland cement paste degradation in boric acid is higher than in pure water, regarding the degraded depths measured and calcium leaching rate. This observation has been confirmed by solid characterization. Microstructure analysis of degraded Portland cement paste showed a global porosity increase in the degraded zone that might be mainly attributed to Portlandite dissolution. An Ettringite reprecipitation in the degraded zone has been suspected but could also be Ettringite-like phases containing boron. The analysis techniques used did not allow us to differentiate it, and no others specific mineral phases containing boron has been identified. Profile pattern by XRD analysis allowed us to identify four zones composing the degraded Portland cement paste

  16. Experimental observations of boric acid precipitation scenarios

    Energy Technology Data Exchange (ETDEWEB)

    Vaghetto, R., E-mail: r.vaghetto@tamu.edu; Childs, M., E-mail: masonchilds@tamu.edu; Jones, P., E-mail: pgjones87@tamu.edu; Lee, S., E-mail: sayalee@tamu.edu; Kee, E., E-mail: erniekee@gmail.com; Hassan, Y.A., E-mail: y-hassan@tamu.edu

    2017-02-15

    During a Loss of Coolant Accident (LOCA) in Light Water Reactors (LWR), borated water is injected into the core through the safety injection system. The continuous vaporization of the water from the core may increase the concentration of boric acid in the core that, under certain conditions may reach the solubility limit and precipitate. This includes scenarios where the liquid water supply to the core is affected by possible blockages due to debris accumulation. Questions have been raised on the effects of the precipitate in the core on the flow behavior, including the possibility of additional blockages produced by precipitate accumulation. A simple experimental facility was constructed to perform experimental observations of the behavior of borated water under the combined effects of the boiling and the boric acid precipitation (BAP). The facility consists of a transparent polycarbonate vertical pipe where forty-five heated rods have been installed to supply the power to the water to reach the saturation temperature, and maintain a desired boil-off rate. The layout and geometry of the experimental apparatus were conceived to emulate a simplified core of a Pressurized Water Reactor (PWR). Experimental observations have been conducted under two different conditions. Preliminary tests were conducted to observe the behavior of the water and the boric acid precipitate during a boil-off scenario without borated water addition (decreasing water level). During the main test runs, borated water was constantly injected from the top of the test section to maintain a constant mixture level in the test section. Both tests assumed no flow from the bottom of the test section which may be the case of PWR LOCA scenarios in presence of debris-generated core blockage. The observations performed with a set of cameras installed around the test section showed interesting effects of the vapor bubbles on the boric acid precipitate migration and accumulation in the test section. The

  17. Boric Acid Corrosion of Concrete Rebar

    Directory of Open Access Journals (Sweden)

    Yang L.

    2013-07-01

    Full Text Available Borated water leakage through spent fuel pools (SFPs at pressurized water reactors is a concern because it could cause corrosion of reinforcement steel in the concrete structure and compromise the integrity of the structure. Because corrosion rate of carbon steel in concrete in the presence of boric acid is lacking in published literature and available data are equivocal on the effect of boric acid on rebar corrosion, corrosion rate measurements were conducted in this study using several test methods. Rebar corrosion rates were measured in (i borated water flowing in a simulated concrete crack, (ii borated water flowing over a concrete surface, (iii borated water that has reacted with concrete, and (iv 2,400 ppm boric acid solutions with pH adjusted to a range of 6.0 to 7.7. The corrosion rates were measured using coupled multielectrode array sensor (CMAS and linear polarization resistance (LPR probes, both made using carbon steel. The results indicate that rebar corrosion rates are low (~1 μm/yr or lesswhen the solution pH is ~7.1 or higher. Below pH ~7.1, the corrosion rate increases with decreasing pH and can reach ~100 μm/yr in solutions with pH less than ~6.7. The threshold pH for carbon steel corrosion in borated solution is between 6.8 and 7.3.

  18. Esterification of microcrystalline cellulose by binary mixture of pyromellitic dianhydride and boric acid

    International Nuclear Information System (INIS)

    Arslanov, Sh.S.; Petropavlovskij, G.A.

    1996-01-01

    The reaction between microcrystalline cellulose and boric acid in the medium of dimethyl-sulfoxide (DMSO) and in solid phase has been studied. By the methods of IR and 1 H NMR spectroscopy it has been shown that the triatment of cellulose with boric acid solution in DMSO, while the latter is removed under vacuum conditions and cellulose is heated up to 170 deg C, gives rise to formation of unstable esters of cellulose and boric acid. Pyromellitate-borates of cellulose are formed in the course of cellulose reaction with a mixture of boric acid and pyromellite dianhydride. 9 refs., 3 figs., 1 tab

  19. Zinc-Nickel Codeposition in Sulfate Solution Combined Effect of Cadmium and Boric Acid

    Directory of Open Access Journals (Sweden)

    Y. Addi

    2011-01-01

    Full Text Available The combined effect of cadmium and boric acid on the electrodeposition of zinc-nickel from a sulfate has been investigated. The presence of cadmium ion decreases zinc in the deposit. In solution, cadmium inhibits the zinc ion deposition and suppresses it when deposition potential value is more negative than −1.2 V. Low concentration of CdSO4 reduces the anomalous nature of Zn-Ni deposit. Boric acid decreases current density and shifts potential discharge of nickel and hydrogen to more negative potential. The combination of boric acid and cadmium increases the percentage of nickel in the deposit. Boric acid and cadmium.

  20. Enriched boric acid as an optimized neutron absorber in the EPR primary coolant

    International Nuclear Information System (INIS)

    Cosse, Christelle; Jolivel, Fabienne; Berger, Martial

    2012-09-01

    reasons, the EBA Boron 10 isotopic atomic abundance target value is 37 at.%. However, EBA conditioning also necessitates the renewal of boric acid supply, operating and management schemes. Supplies must cover the needs for initial conditioning and for later compensation of losses during operation. These losses can be divided into three categories: 1. volumetric losses (such as leaks) 2. decrease of total Boron concentration (dilution for example) 3. Boron neutron core depletion (through Boron 10 consuming reactions). The first two losses are classically compensated with EBA supplied with the required isotopic abundance. Very Enriched boric acid (VEBA) will also be supplied to compensate Boron 10 enrichment losses due to neutron depletion ( 10 B [n, He] 7 Li). According to an optimized boron neutron depletion management scheme, neutron depletion will be directly compensated into boric acid make-up tanks prior to any refuelling shutdown, by injection of reasonable quantities of VEBA (Boron 10 atomic abundance superior to 90 at.%). Finally, EPR operators and chemists will have to cope with these two different sorts of boric acid. Distinctive methods will be employed to avoid any error: use of an optimized and strict policy of different units of Boron used in instrumentation and control systems and in operating procedures; distinct packaging and storage; separate procedures; specific skills for Boron neutron core depletion management. EPR operation has to rely on appropriate parameters and procedures. Total Boron concentration and Boron 10 isotopic abundance monitoring will be periodically achieved by sampling and analysing all borated systems, so called 'boron mapping'. The Boron 10 concentration is continuously monitored in the reactor coolant system with the on-line neutronic boron meter located in the Nuclear Sampling System (NSS): this data is directly used for reactor operation and chemistry control. The use of EBA in the EPR is one of the major progresses for

  1. Surface interactions of cesium and boric acid with stainless steel

    International Nuclear Information System (INIS)

    Grossman-Canfield, N.

    1995-08-01

    In this report, the effects of cesium hydroxide and boric acid on oxidized stainless steel surfaces at high temperatures and near one atmosphere of pressure are investigated. This is the first experimental investigation of this chemical system. The experimental investigations were performed using a mass spectrometer and a mass electrobalance. Surfaces from the different experiments were examined using a scanning electron microscope to identify the presence of deposited species, and electron spectroscopy for chemical analysis to identify the species deposited on the surface. A better understanding of the equilibrium thermodynamics, the kinetics of the steam-accelerated volatilizations, and the release kinetics are gained by these experiments. The release rate is characterized by bulk vaporization/gas-phase mass transfer data. The analysis couples vaporization, deposition, and desorption of the compounds formed by cesium hydroxide and boric acid under conditions similar to what is expected during certain nuclear reactor accidents. This study shows that cesium deposits on an oxidized stainless steel surface at temperatures between 1000 and 1200 Kelvin. Cesium also deposits on stainless steel surfaces coated with boric oxide in the same temperature ranges. The mechanism for cesium deposition onto the oxide layer was found to involve the chemical reaction between cesium and chromate. Some revaporization in the cesium hydroxide-boric acid system was observed. It has been found that under the conditions given, boric acid will react with cesium hydroxide to form cesium metaborate. A model is proposed for this chemical reaction

  2. Effects of boric acid and borax on titanium dioxide genotoxicity.

    Science.gov (United States)

    Turkez, Hasan

    2008-07-01

    Titanium dioxide (TiO(2)) is a potential carcinogenic/mutagenic agent although it is used in many areas including medical industries and cosmetics. Boron (as boric acid and borax) has also well-described biological effects and therapeutic benefits. In a previous study, sister-chromatid exchanges (SCEs) and micronuclei (MN) rates were assessed in control and TiO(2)-treated (1, 2, 3, 5, 7.5 and 10 microm) human whole blood cultures. The results showed that the rates of SCE (at 2, 3, 5, 7.5 and 10 microm) and MN (at 5, 7.5 and 10 microm) formation in peripheral lymphocytes were increased significantly by TiO(2) compared with the controls. The present study also investigated the genetic effects of boric acid and borax (2.5, 5 and 10 microm) on cultures with and without TiO(2) addition. No significant increase in SCE and MN frequencies were observed at all concentrations of boron compounds. However, TiO(2)-induced SCE and MN could be reduced significantly by the presence of boric acid and borax. In conclusion, this study indicated for the first time that boric acid and borax led to an increased resistance of DNA to damage induced by TiO(2). 2008 John Wiley & Sons, Ltd

  3. Boric acid - trilon B (glycine, acetylurea) - water systems at 25 deg C

    International Nuclear Information System (INIS)

    Skvortsov, V.G.; Rodionov, N.S.; Molodkin, A.K.; Fedorov, Yu.A.; Tsekhanskij, R.S.

    1985-01-01

    Boric acid-trilon B (glycine, acetylurea)-water systems are studied at 25 deg C by the methods of isothermal solubility densi- and refractometry. It is ascertained that all of them are of a simple eutonic type with a small salting-out effect of organic components on boric acid

  4. Boric acid - trilon B (glycine, acetylurea) - water systems at 25 deg C

    Energy Technology Data Exchange (ETDEWEB)

    Skvortsov, V G; Rodionov, N S; Molodkin, A K; Fedorov, Yu A; Tsekhanskij, R S

    1985-07-01

    Boric acid-trilon B (glycine, acetylurea)-water systems are studied at 25 deg C by the methods of isothermal solubility densi- and refractometry. It is ascertained that all of them are of a simple eutonic type with a small salting-out effect of organic components on boric acid.

  5. Impacts of impregnation with boric acid and borax on the red colour ...

    African Journals Online (AJOL)

    Impacts of impregnation with boric acid and borax on the red colour tone of some hardwoods and varnishes. H Keskin, M Atar, A Ketizmen. Abstract. This study was performed to determine the impacts of impregnation with boric acid and borax on the red colour tone of some hardwoods and varnishes. For this purpose, the ...

  6. CEC mechanism in electrochemical oxidation of nitrocatechol-boric acid complexes

    International Nuclear Information System (INIS)

    Rafiee, Mohammad; Nematollahi, Davood; Salehzadeh, Hamid

    2011-01-01

    Graphical abstract: Display Omitted Highlights: → Nitrochetechol and its anionic form undergo complex reaction with boric acid. → The electron transfer of complex is coupled with both proceeding and following chemical reactions. → Electrochemical behavior of complex is resolved by diagnostic criteria and digital simulation. - Abstract: The electrochemical behavior of nitrocatechols-boric acid complexes in aqueous solution has been studied using cyclic voltammetry. The results indicate that nitrocatechol-boric acid complex derivatives are involved in the CEC mechanism. In this work, the impact of empirical parameters on the shape of the voltammograms is examined based on a CEC mechanism. In addition, homogeneous rate constants of both the preceding and the following reactions were estimated by comparing the experimental cyclic voltammograms with the digitally simulated results. The calculated dissociation constants for the complexes (K d ) and for ring cleavage of nitroquinone (k f2 ) were found to vary in the following order: 4-nitrocatechol > 3-methylnitrocatechol > 3-metoxynitrocatechol.

  7. 40 CFR 180.1121 - Boric acid and its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Boric acid and its salts, borax... salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate, boric oxide (boric anhydride... its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate, boric oxide (boric...

  8. Removal of Aqueous Boron by Using Complexation of Boric Acid with Polyols: A Raman Spectroscopic Study

    Energy Technology Data Exchange (ETDEWEB)

    Eom, Ki Heon; Jeong, Hui Cheol; An, Hye Young; Lim, Jun-Heok; Lee, Jea-Keun; Won, Yong Sun [Pukyong National University, Busan (Korea, Republic of)

    2015-12-15

    Boron is difficult to be removed from seawater by simple RO (reverse osmosis) membrane process, because the size of boric acid (B(OH){sub 3}), the major form of aqueous boron, is as small as the nominal pore size of RO membrane. Thus, the complexation of boric acid with polyols was suggested as an alternative way to increase the size of aqueous boron compounds and the complexation behavior was investigated with Raman spectroscopy. As a reference, the Raman peak for symmetric B-O stretching vibrational mode both in boric acid and borate ion (B(OH){sub 4}{sup -}) was selected. A Raman peak shift (877 cm{sup -1} →730 cm{sup -1}) was observed to confirm that boric acid in water is converted to borate ion as the pH increases, which is also correctly predicted by frequency calculation. Meanwhile, the Raman peak of borate ion (730 cm{sup -1}) did not appear as the pH increased when polyols were applied into aqueous solution of boric acid, suggesting that the boric acid forms complexing compounds by combining with polyols.

  9. Preliminary Evaluation Of DWPF Impacts Of Boric Acid Use In Cesium Strip FOR SWPF And MCU

    International Nuclear Information System (INIS)

    Stone, M.

    2010-01-01

    A new solvent system is being evaluated for use in the Modular Caustic-Side Solvent Extraction Unit (MCU) and in the Salt Waste Processing Facility (SWPF). The new system includes the option to replace the current dilute nitric acid strip solution with boric acid. To support this effort, the impact of using 0.01M, 0.1M, 0.25M and 0.5M boric acid in place of 0.001M nitric acid was evaluated for impacts on the DWPF facility. The evaluation only covered the impacts of boric acid in the strip effluent and does not address the other changes in solvents (i.e., the new extractant, called MaxCalix, or the new suppressor, guanidine). Boric acid additions may lead to increased hydrogen generation during the SRAT and SME cycles as well as change the rheological properties of the feed. The boron in the strip effluent will impact glass composition and could require each SME batch to be trimmed with boric acid to account for any changes in the boron from strip effluent additions. Addition of boron with the strip effluent will require changes in the frit composition and could lead to changes in melt behavior. The severity of the impacts from the boric acid additions is dependent on the amount of boric acid added by the strip effluent. The use of 0.1M or higher concentrations of boric acid in the strip effluent was found to significantly impact DWPF operations while the impact of 0.01M boric acid is expected to be relatively minor. Experimental testing is required to resolve the issues identified during the preliminary evaluation. The issues to be addressed by the testing are: (1) Impact on SRAT acid addition and hydrogen generation; (2) Impact on melter feed rheology; (3) Impact on glass composition control; (4) Impact on frit production; and (5) Impact on melter offgas. A new solvent system is being evaluated for use in the Modular Caustic-Side Solvent Extraction Unit (MCU) and in the Salt Waste Processing Facility (SWPF). The new system includes the option to replace the

  10. KLM's boric acid reclamation system (BARS). An update

    International Nuclear Information System (INIS)

    Schuelke, D.; Kniazewycz, B.G.; Markind, J.; Brossart, M.A.; Choi, R.C.

    1987-01-01

    KLM Technologies has implemented its Department of Energy Phase II Small Business Innovative Research (SBIR) demonstration program for a radioactive waste Boric Acid Reclamation System (BARS). Preliminary performance indicates enhanced treatment by the BARS technique over state of the art process methods for selective removal of silica and other impurities from borated water matrices. At optimal system recovery of 96-97 percent. BARS removes nominal levels of boric acid while achieving significant rejection for soluble silica and selective radioisotopes. This is indicative of superior performance compared to existing data governing standard boric acid process treatment in the presence of silica and other contaminants. Conventional technologies have also proven to be relatively expensive, utilizing costly chemically treated disposable resins for primary waste removal. The overall BARS program indicates substantial savings regarding off-site disposal costs based on reduced waste generation. Optimization of the BARS technology could have potential impact on conventional process technologies that are essentially non-selective in removal capacities. Within the scope of the project, a variety of contaminated process stream and mixed radwaste sources have been evaluated at Northern States Power's Prairie Island Nuclear Generating Station. The design of an advanced prototype BARS as an optimized process alternative was the result of KLM's initial Phase 1 SBIR program with the DOE in 1984 and 1985

  11. Evaluation of ultrasonic technique to characterize the concentration of boric acid in liquid medium

    International Nuclear Information System (INIS)

    Kohara, Richard Yuzo Ramida

    2015-01-01

    This dissertation is to analyze the viability of using ultrasonic technique to characterize the concentration of boric acid in liquid medium non-invasively, therefore, ultrasonic tests were performed relating different boric acid concentrations with the travel time of the ultrasonic wave, also were evaluated factors able to mask the characterization of these concentrations by ultrasonic technique. The results showed that the ultrasonic technique allows the characterization of boric acid concentrations in liquid medium in very simple terms by the ultrasonic wave travel time, requiring further studies in complex conditions. (author)

  12. Device for regulating light water nuclear reactors by changing the boric acid concentration in the cooling water circuit

    International Nuclear Information System (INIS)

    Brown, W.W.; Van der Schoot, M.R.

    1980-01-01

    Small changes in boric acid concentration can be carried out quickly by a combination of an ion exchanger with temperature-dependent capacity and an evaporator. No boric acid need be extracted from the circuit or added to it. However, if large changes of concentration are required, boric acid has to be added. The evaporator is then used to separate distilled water and concentrated boric acid when the cooling water is diluted. (DG) [de

  13. Chloride stress corrosion cracking of Alloy 600 in boric acid solutions

    International Nuclear Information System (INIS)

    Berge, Ph.; Noel, D.; Gras, J.M.; Prieux, B.

    1997-10-01

    The high nickel austenitic alloys are generally considered to have good resistance to chloride stress corrosion cracking. In the standard boiling magnesium chloride solution tests, alloys with more than 40% nickel are immune. Nevertheless, more recent data show that cracking can occur in both Alloys 600 and 690 if the solution is acidified. In other low pH media, such as boric acid solution at 100 deg C, transgranular and intergranular cracking are observed in Alloy 600 in the presence of minor concentrations of sodium chloride (2g/I). In concentrated boric acid at higher temperatures (250 and 290 deg C), intergranular cracking also occurs, either when the chloride concentration is high, or at low chloride contents and high oxygen levels. The role of pH and a possible specific action of boric acid are discussed, together with the influence of electrochemical potential. (author)

  14. Boric acid - ammonium rhodanide (nitrate, sulfate) - water system at 25 deg C

    Energy Technology Data Exchange (ETDEWEB)

    Skvortsov, V G; Molodkin, A K; Tsekhanskij, R S; Sadetdinov, Sh V; Nikonov, F V [Chuvashskij Gosudarstvennyj Pedagogicheskij Inst., Cheboksary (USSR); Universitet Druzhby Narodov, Moscow (USSR))

    1985-03-01

    Methods of isothermal solubility and refractometry have been used to establish that boric acid-ammonium rhodanite (nitrate, sulfate) - water systems are of a simple eutonic type. Rhodanide salts out boric acid, while nitrate and sulfate salt it in. The lyotropic effect referred to the volumetric share of both anion and cation increases in the series SCN/sup -/ < NO/sub 3//sup -/ < SO/sub 4//sup 2 -/.

  15. Application of Lime Additive on Cementation of Concentrated Low Activities Liquid Radwaste Containing Boric Acid

    International Nuclear Information System (INIS)

    Bahdir-Johan

    2000-01-01

    The effect of lime additive on the waste form containing boric acid and the activity 1 μCi/ml have been studied. The studying parameter was the optimum lime additive in concentrate. The sample was made by cement slurry containing boric acid. The cement slurry composition are water/cement ratio (W/C) was 0.35, sand/cement ratio (S/C) was 0.75 and boric (B) was 15000 ppm. On this condition into cement slurry was added the lime additive (K/C) 0.05 -0.8 by weigh. The quality test included density, compressive strength and leaching rate. The density was determination by weighing and measuring sample volume, compressive strength determination using Paul Weber apparatus and leaching rate tested using aquadest. The result of this research are the lime/cement ratio (K/C) 0.30; the density (ρ) 2.449 ± 0.008 g.cm -3 , the compressive strength (Γ) 44.005 ± 0.012 N.mm -2 and the leaching rate (Rn) 7.20x10 -4 -0.90x10 -4 g.cm -2 day -1 . According to this research the quality of the waste form has been complied the IAEA quality standard. (author)

  16. The boric acid - ammonium rhodanide (nitrate, sulfate) - water system at 25 deg C

    International Nuclear Information System (INIS)

    Skvortsov, V.G.; Molodkin, A.K.; Tsekhanskij, R.S.; Sadetdinov, Sh.V.; Nikonov, F.V.

    1985-01-01

    Methods of isothermal solubility and refractometry have been used to establish that boric acid-ammonium rhodanite (nitrate, sulfate) - water systems are of a simple eutonic type. Rhodanide salts out boric acid, while nitrate and sulfate salt it in. The lyotropic effect referred to the volumetric share of both anion and cation increases in the series SCN - 3 - 4 2-

  17. Ingested boric acid effect on the venom chemistry of Solenopsis invicta Buren (Hymenoptera: Formicidae)

    Science.gov (United States)

    During a field evaluation of a boric acid bait against the red imported fire ant, Solenopsis invicta Buren, it was observed that workers of intoxicated colonies produced stings with less toxic effects compared to workers from healthy colonies. In this study, the effect of boric acid on the levels o...

  18. PERIODS OF VERTEBRAL COLUMN SENSITIVITY TO BORIC ACID TREATMENT IN CD-1 MICE IN UTERO

    Science.gov (United States)

    Periods of vertebral column sensitivity to boric acid treatment in CD-1 mice in utero.Cherrington JW, Chernoff N.Department of Toxicology, North Carolina State University, Raleigh, NC 27695, USA. jana_cherrington@hotmail.comBoric acid (BA) has many uses as...

  19. 40 CFR 721.3031 - Boric acid (H3BO3), zinc salt (2=3).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Boric acid (H3BO3), zinc salt (2=3). 721.3031 Section 721.3031 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.3031 Boric acid (H3BO...

  20. Effect of nano-silver and boric acid on extending the vase life of cut rose (Rosa hybrida L.).

    Science.gov (United States)

    Hashemabadi, Davood; Liavali, Mahbanoo Hoseinzadeh; Kaviani, Behzad; Mousavi, Meysam; Keyghobadi, Saghi; Zahiri, Samaneh

    2014-09-01

    Silver nano-particles (2-5 nm diam.), as antimicrobial agent and boric acid, as ethylene production inhibitor are used for enhancing the quality and vase life of cut flowers. In the present study the effects of a preservative solution containing nano-silver and boric acid on some traits of cut rose (Rosa hybrida L. cv. Yellow Island) including vase life, ethylene production, dry weight percentage, chlorophyll content, flower opening index, beta-carotene of petals and the number of basal stem end bacteria were investigated. The results showed that the effect of nano-silver and boric acid as either solitary or in combination with each other were significant (p rose treated with 100 mg l(-1) boric acid along with 5 mg l(-1) nano-silver. The lowest number of bacteria in the end of stem was calculated in cut flowers treated with the highest concentrations of boric acid (300 mg l(-1)) and nano-silver (20 mg l(-1)).

  1. Effects of an inorganic insecticide (boric acid) against Blattella ...

    African Journals Online (AJOL)

    ufuoma

    2013-05-01

    May 1, 2013 ... Data on ovarian .... The overall data suggested an interference of boric acid with the ... solutions as baits for management of German cockroaches .... Comp. Biochem. Physiol. 135C:257-267. Tine S, Aribi N, Soltani N (2011).

  2. Electrodialysis recovery of boric acid and potassium hydroxide from eluates of SWC facilities at NPP with VVER

    International Nuclear Information System (INIS)

    Dudnik, S.N.; Virich, P.M.; Kramskikh, E.Y.; Masanov, O.L.; Turovsky, I.P.

    1993-01-01

    To extract boric acid and potassium hydroxide from regenerates of SWC-2-46 facilities, an electrodialysis-sorption process has been devised consisting of the following operations: separation of boron-alkaline regenerate solution into desorbate and wash water; filling of desalination and concentration chambers, respectively, with desorbate and was water of electrodialysis equipment; production of boric acid and potassium hydroxide from desorbate by electrodialysis; removal of chloride-ion from boric acid solution on ion-exchange filter AB-17-18. The flow-sheet was tested and boron containing alkaline regeneration solutions were recovered from Novovoronezh NPP

  3. Effect of boric acid mass transfer on the accumulation thereof in a fuel core under emergency modes at NPPs with WMR

    Science.gov (United States)

    Morozov, A. V.; Sorokin, A. P.; Ragulin, S. V.; Pityk, A. V.; Sahipgareev, A. R.; Soshkina, A. S.; Shlepkin, A. S.

    2017-07-01

    Boric acid mass transfer processes in the reactor facilities with WMR are considered for the case of an emergency with breaking of the main circulation pipeline (MCP) and the operation of the passive safety systems, such as first-, second-, and third-stage accumulator tank systems, and a passive heat removal system (PHRS). Calculation results are presented for a change in the boric acid concentration in the fuel core (FC) of a water-moderated reactor (WMR) in the case of an emergency process. The calculations have been performed for different values of drop entrainment of boric acid from the reactor (0, 0.2, 2%). A substantial excess of the maximum concentration of boric acid has been found to occur 24 hours after an emergency event with a break of MCP. It is shown that increasing the droplet entrainment of boric acid causes the crystallization and accumulation thereof in the FC to become slower. The mass of boric acid deposits on the elements of internals is determined depending on the values of drop entrainment. These results allow one to draw a conclusion concerning the possibility of accumulation and crystallization of boric acid in the FC, because the latter event could lead to a blocking of the flow cross section and disturbance in the heat removal from fuel elements. A review of available literature data concerning the thermal properties of boric acid solution (density, viscosity, thermal conductivity) is presented. It is found that the available data are of quite a general character, but it does not cover the entire range of parameters (temperature, pressure, acid concentrations) inherent in a possible emergency situation at nuclear power plants with WMR. It is demonstrated that experimental study of boric acid drop entrainment at the parameters inherent in the emergency mode of WMR operation, as well as the studies of boric acid thermal properties in a wide range of concentrations, are required.

  4. Management of Azole-Refractory Candida Species Using Boric Acid

    African Journals Online (AJOL)

    Mgina

    commonly used drugs in the country, the best performance of boric acid envisage the need to update the national ... drugs especially with the azole antifungal groups and are ... Other factors include extensive use of broad spectrum ..... influence not only prescription tendency but .... pharmacokinetics, and antifungal therapy.

  5. Breaking Bad Delirium: Methamphetamine and Boric Acid Toxicity with Hallucinations and Pseudosepsis.

    Science.gov (United States)

    Johnson, Kayla; Stollings, Joanna L; Ely, E Wesley

    2017-02-01

    A 30-year-old patient presented with hallucinations and profound shock. He was initially misdiagnosed as having severe sepsis; once ingestions were considered, he was diagnosed as potentially having arsenic toxicity. The clinical story reveals many instructional lessons that could aid in the evaluation and management of future patients. This man presented with large amounts of blue crystals around his nose and lips from inhaling and eating boric acid (an ant poison) so he could, as he put it, kill the ants "pouring into my mouth and nose and up into my brain." His profound pseudosepsis and sustained delirium were induced by co-ingestion of methamphetamine and a large quantity of boric acid. Delirium is a form of acute brain dysfunction that often is multifactorial in critical illness and, when seen in septic shock, is associated with prolonged mechanical ventilation, increased length of hospital stay, medical costs, higher mortality, and long-term cognitive impairment resembling dementia. Pseudosepsis is a noninfectious condition most commonly seen with ingestions such as salicylate (aspirin) toxicity. This report emphasizes the need to recognize agents that contain boric acid as an etiology of unexplained delirium and profound shock.

  6. Effect of Silica Sol on Boric-sulfuric Acid Anodic Oxidation of LY12CZ Aluminum Alloy

    Directory of Open Access Journals (Sweden)

    LIU Hui-cong

    2016-07-01

    Full Text Available Aluminum alloy anodizing coatings were prepared for LY12CZ in the boric-sulfuric acid solution (45g/L sulfuric acid,8g/L boric acid with the addition of 10%,20%,30% (volume fractionsilica sol,with the gradient voltage of 15V. The current and voltage transients of the anodizing process were collected by data collection instrument. The surface morphologies,microstructure and chemical composition of the anodic coatings were characterized by scanning electron microscopy (SEM. The corrosion resistance was examined by neutral salt spray,electrochemical impedance spectroscopy (EIS test and titrating test. The results show that the different concentration of silica sol addition can influence the forming and dissolution of anodizing coatings,improve the compactness smoothness and corrosion resistance during the anodizing process in the boric-sulfuric acid solution.

  7. Synergy of boric acid and added salts in the catalytic dehydration of hexoses to 5-hydroxymethylfurfural in water

    DEFF Research Database (Denmark)

    Hansen, Thomas Steen; Mielby, Jerrik Jørgen; Riisager, Anders

    2011-01-01

    Boric acid and salts showed a synergistic effect on the dehydration of concentrated aqueous sugar solutions to yield 5-hydroxymethylfurfural.......Boric acid and salts showed a synergistic effect on the dehydration of concentrated aqueous sugar solutions to yield 5-hydroxymethylfurfural....

  8. The characterisation of molecular boric acid by mass spectrometry and matrix isolation-infrared spectroscopy

    International Nuclear Information System (INIS)

    Ogden, J.S.; Young, N.A.; Bowsher, B.R.

    1987-10-01

    Boric acid (H 3 BO 3 ) is used as a soluble neutron absorber in the coolant of pressurised water reactors and will be an important species in defining the fission product chemistry of severe reactor accidents. Mass spectrometry and matrix isolation-infrared spectroscopy have been used to characterise boric acid in the vapour phase and hence assess the implications of any chemical interactions. Crystalline orthoboric acid vaporises to yield molecular H 3 BO 3 when heated in vacuum to approximately 40 0 C. The infrared spectrum of the vapour species isolated in low-temperature nitrogen matrices shows characteristic absorptions at 3668.5 (E'), 1426.2 (E'), 1009.9 (E'), 675.0 (A''), 513.8 (A'') and 448.9 (E') cm -1 , consistent with C 3h symmetry. These spectral assignments are supported by extensive isotope labelling, and by a partial normal co-ordinate analysis. These data will be used to quantify specific thermodynamic functions and hence assist in determining the magnitude of reactions such as boric acid with caesium iodide. (author)

  9. Mitochondrial dysfunction is involved in the toxic activity of boric acid against Saprolegnia.

    Directory of Open Access Journals (Sweden)

    Shimaa E Ali

    Full Text Available There has been a significant increase in the incidence of Saprolegnia infections over the past decades, especially after the banning of malachite green. Very often these infections are associated with high economic losses in salmonid farms and hatcheries. The use of boric acid to control the disease has been investigated recently both under in vitro and in vivo conditions, however its possible mode of action against fish pathogenic Saprolegnia is not known. In this study, we have explored the transformation in Saprolegnia spores/hyphae after exposure to boric acid (1 g/L over a period 4-24 h post treatment. Using transmission electron microscopy (TEM, early changes in Saprolegnia spores were detected. Mitochondrial degeneration was the most obvious sign observed following 4 h treatment in about 20% of randomly selected spores. We also investigated the effect of the treatment on nuclear division, mitochondrial activity and function using confocal laser scanning microscopy (CLSM. Fluorescence microscopy was also used to test the effect of treatment on mitochondrial membrane potential and formation of reactive oxygen species. Additionally, the viability and proliferation of treated spores that correlated to mitochondrial enzymatic activity were tested using an MTS assay. All obtained data pointed towards changes in the mitochondrial structure, membrane potential and enzymatic activity following treatment. We have found that boric acid has no effect on the integrity of membranes of Saprolegnia spores at concentrations tested. It is therefore likely that mitochondrial dysfunction is involved in the toxic activity of boric acid against Saprolegnia spp.

  10. Study of structural, surface and hydrogen storage properties of boric acid mediated metal (sodium)-organic frameworks

    Science.gov (United States)

    Ozer, Demet; Köse, Dursun A.; Sahin, Onur; Oztas, Nursen A.

    2018-04-01

    Three boric acid mediated metal organic frameworks were synthesized by solution method with using succinic acid, fumaric acid and acetylene dicarboxylic acid as a ligand source and sodium as a metal source. The complexes were characterized by FT-IR, powder XRD, elemental analyses and single crystal measurements. The complexes with the formula, C4H18B2Na2O14, C4H16B2Na2O14 and C4H14B2Na2O14 were successfully obtained. BET surface area of complexes were calculated and found as 13.474 m2/g for catena-(tetrakis(μ2-hydroxo)-(μ2-trihydrogen borate)-(μ2-succinato)-di-sodium boric acid solvate), 1.692 m2/g for catena-(tetrakis(μ2-hydroxo)-(μ2-trihydrogen borate)-(μ2-fumarato)-di-sodium boric acid solvate) and 5.600 m2/g for catena-(tetrakis(μ2-hydroxo)-(μ2-trihydrogen borate)-(μ2-acetylenedicarboxylato)-di-sodium boric acid solvate). Hydrogen storage capacities of the complexes were also studied at 77 K 1 bar pressure and found as 0.108%, 0.033%, 0.021% by mass. When different ligands were used, the pore volume, pore width and surface area of the obtained complexes were changed. As a consequence, hydrogen storage capacities also changed.

  11. Activity of boric acid on German cockroaches: Analysis of residues ...

    African Journals Online (AJOL)

    STORAGESEVER

    2009-02-18

    Feb 18, 2009 ... Full Length Research Paper. Activity of ... In a previous study, we have shown that boric ... ing 300 µl of curcumin solution (12.5 mg curcumin, 10 ml acetic acid) ..... Schal C, Chiang AS, Burns EL, Gadot M, Cooper RA (1993).

  12. Inhibition studies of soybean (Glycine max) urease with heavy metals, sodium salts of mineral acids, boric acid, and boronic acids.

    Science.gov (United States)

    Kumar, Sandeep; Kayastha, Arvind M

    2010-10-01

    Various inhibitors were tested for their inhibitory effects on soybean urease. The K(i) values for boric acid, 4-bromophenylboronic acid, butylboronic acid, and phenylboronic acid were 0.20 +/- 0.05 mM, 0.22 +/- 0.04 mM, 1.50 +/- 0.10 mM, and 2.00 +/- 0.11 mM, respectively. The inhibition was competitive type with boric acid and boronic acids. Heavy metal ions including Ag(+), Hg(2+), and Cu(2+) showed strong inhibition on soybean urease, with the silver ion being a potent inhibitor (IC(50) = 2.3 x 10(-8) mM). Time-dependent inhibition studies exhibited biphasic kinetics with all heavy metal ions. Furthermore, inhibition studies with sodium salts of mineral acids (NaF, NaCl, NaNO(3), and Na(2)SO(4)) showed that only F(-) inhibited soybean urease significantly (IC(50) = 2.9 mM). Competitive type of inhibition was observed for this anion with a K(i) value of 1.30 mM.

  13. Galvanic corrosion between carbon steel 1018 and Alloy 600 in crevice with boric acid solution

    International Nuclear Information System (INIS)

    Kim, Dong Jin; Kim, Hong Pyo; Kim, Joung Soo; Machonald, Digby D.

    2005-01-01

    This work dealt with the evaluation of galvanic corrosion rate in a corrosion cell having annular gap of 0.5 mm between carbon steel 1018 and alloy 600 as a function of temperature and boron concentration. Temperature and boron concentration were ranged from 110 to 300 .deg. C and 2000∼10000 ppm, respectively. After the operating temperature of the corrosion cell where the electrolyte was injected was attained at setting temperature, galvanic coupling was made and at the same time galvanic current was measured. The galvanic corrosion rate decreased with time, which was described by corrosion product such as protective film as well as boric acid deposit formed on the carbon steel with time. From the galvanic current obtained as a function of temperature and boron concentration, it was found that the galvanic corrosion rate decreased with temperature while the corrosion rate increased with boron concentration. The experimental results obtained from galvanic corrosion measurement were explained by adhesive property of corrosion product such as protective film, boric acid deposit formed on the carbon steel wall and dehydration of boric acid to be slightly soluble boric acid phase. Moreover the galvanic corrosion rate calculated using initial galvanic coupling current instead of steady state coupling current was remarked, which could give us relatively closer galvanic corrosion rate to real pressurized water reactor

  14. Is Boric Acid Toxic to Reproduction in Humans? Assessment of the Animal Reproductive Toxicity Data and Epidemiological Study Results.

    Science.gov (United States)

    Duydu, Yalçın; Başaran, Nurşen; Ustündağ, Aylin; Aydın, Sevtap; Undeğer, Ulkü; Ataman, Osman Yavuz; Aydos, Kaan; Düker, Yalçın; Ickstadt, Katja; Waltrup, Brita Schulze; Golka, Klaus; Bolt, Hermann Maximilian

    2016-01-01

    Boric acid and sodium borates are classified as toxic to reproduction in the CLP Regulation under "Category 1B" with the hazard statement of "H360FD". This classification is based on the reprotoxic effects of boric acid and sodium borates in animal experiments at high doses. However, boron mediated reprotoxic effects have not been proven in epidemiological studies so far. The epidemiological study performed in Bandırma boric acid production plant is the most comprehensive published study in this field with 204 voluntarily participated male workers. Sperm quality parameters (sperm morphology, concentration and motility parameters), FSH, LH and testosterone levels were determined in all participated employees as the reproductive toxicity biomarkers of males. However, boron mediated unfavorable effects on reproduction in male workers have not been determined even in the workers under very high daily boron exposure (0.21 mg B/kg-bw/day) conditions. The NOAEL for rat reproductive toxicity is equivalent to a blood boron level of 2020 ng/g. This level is higher than the mean blood boron concentration (223.89 ± 69.49 ng/g) of the high exposure group workers in Bandırma boric acid production plant (Turkey) by a factor of 9. Accordingly, classifying boric acid and sodium borates under "Category 1B" as "presumed reproductive human toxicant in the CLP regulation seems scientifically not reasonable. The results of the epidemiological studies (including the study performed in China) support for a down-classification of boric acid from the category 1B, H360FD to category 2, H361d, (suspected of damaging the unborn child).

  15. Enhanced activity of Anticarsia gemmatalis Hüb. (Lepidoptera: Noctuidae) nuclear polyhedrosis virus by boric acid in the laboratory

    OpenAIRE

    Morales, Lauro; Moscardi, Flávio; Sosa-Gómez, Daniel R.; Paro, Fábio E.; Soldorio, Ivanilda L.

    1997-01-01

    Boric acid concentrations (0.02,0.03,0.045,0.067 and 0.101 g/100 ml of diet) were evaluated in combination with the Anticarsia gemmatalis Hüb. nuclear polyhedrosis virus (AgNPV) for enhanced virali activity against the insect. Seven days after inoculation, the median lethal concentration (LC50) was 1.52 x 10(5) for the AgNPV alone and 7.95 x 10² for the NPV mixed with 0.045g of boric acid/100 ml of diet. At subsequent evaluation dates (9,11 and 14 days after inoculation) LC50's for NPV+boric ...

  16. Influence of temperature, hydrogen and boric acid concentration on IGSCC susceptibility of unsensitized 316 stainless steel

    Energy Technology Data Exchange (ETDEWEB)

    Arioka, Koji [Inst. of Nuclear Safety System Inc., Mihama, Fukui (Japan)

    2002-09-01

    IGSCC susceptibility of unsensitized 316SS under PWR primary water was studied as a function of solution temperature, dissolved hydrogen, and boric acid concentration by SSRT test using specimens with cold deformed hump. IGSCC growth rate was dependent on temperature and the obtained activation energy was 21.6K cal/mol. Regarding the influence of dissolved hydrogen, there was a simple monotonic increase in crack growth rate with the increasing hydrogen concentration within the PWR primary water chemistry specifications. Also, there was a remarkable difference in IGSCC susceptibility with regard to the effect to boric acid concentration. Within the tested concentration, the IGSCC susceptibility under high concentrated boric acid solution (2300ppm B) was inhibited in comparison with that under 500ppm B. These temperature and dissolved hydrogen dependencies of IGSCC susceptibility were similar to the literature on published data on irradiated 316SS. Although further study is required to clarify the mechanism, however the similarity of the dependencies suggests that the rate-limited IGSCC process of un-irradiated 316SS is related to that of IASCC. (author)

  17. Boric acid inhibits embryonic histone deacetylases: A suggested mechanism to explain boric acid-related teratogenicity

    International Nuclear Information System (INIS)

    Di Renzo, Francesca; Cappelletti, Graziella; Broccia, Maria L.; Giavini, Erminio; Menegola, Elena

    2007-01-01

    Histone deacetylases (HDAC) control gene expression by changing histonic as well as non histonic protein conformation. HDAC inhibitors (HDACi) are considered to be among the most promising drugs for epigenetic treatment for cancer. Recently a strict relationship between histone hyperacetylation in specific tissues of mouse embryos exposed to two HDACi (valproic acid and trichostatin A) and specific axial skeleton malformations has been demonstrated. The aim of this study is to verify if boric acid (BA), that induces in rodents malformations similar to those valproic acid and trichostatin A-related, acts through similar mechanisms: HDAC inhibition and histone hyperacetylation. Pregnant mice were treated intraperitoneally with a teratogenic dose of BA (1000 mg/kg, day 8 of gestation). Western blot analysis and immunostaining were performed with anti hyperacetylated histone 4 (H4) antibody on embryos explanted 1, 3 or 4 h after treatment and revealed H4 hyperacetylation at the level of somites. HDAC enzyme assay was performed on embryonic nuclear extracts. A significant HDAC inhibition activity (compatible with a mixed type partial inhibition mechanism) was evident with BA. Kinetic analyses indicate that BA modifies substrate affinity by a factor α = 0.51 and maximum velocity by a factor β = 0.70. This work provides the first evidence for HDAC inhibition by BA and suggests such a molecular mechanism for the induction of BA-related malformations

  18. Boric Acid Catalyzed Convenient Synthesis of Benzimidazoles in Aqueous Media

    Directory of Open Access Journals (Sweden)

    Mohammad Reza Poor Heravi

    2013-01-01

    Full Text Available Synthesis of benzimidazoles has been developed by the o-phenylenediamine with aldehydes using boric acid an efficient catalyst under mild reaction conditions in aqueous media. The product is applicable to aryl and heteroaryl aldehydes. This reaction led to the formation of benzimidazoles new derivatives in good yields. The FT-IR, 19F-NMR, 1H-NMR, 13C-NMR spectra and elemental analysis confirm the structure of compounds.

  19. Boric Acid Catalyzed Convenient Synthesis of Benzimidazoles in Aqueous Media

    OpenAIRE

    Poor Heravi, Mohammad Reza; Ashori, Marjan

    2013-01-01

    Synthesis of benzimidazoles has been developed by the o-phenylenediamine with aldehydes using boric acid an efficient catalyst under mild reaction conditions in aqueous media. The product is applicable to aryl and heteroaryl aldehydes. This reaction led to the formation of benzimidazoles new derivatives in good yields. The FT-IR, 19F-NMR, 1H-NMR, 13C-NMR spectra and elemental analysis confirm the structure of compounds.

  20. Genotoxic effects of boric acid and borax in zebrafish, Danio rerio using alkaline comet assay.

    Science.gov (United States)

    Gülsoy, Nagihan; Yavas, Cüneyd; Mutlu, Özal

    2015-01-01

    The present study is conducted to determine the potential mechanisms of Boron compounds, boric acid (BA) and borax (BX), on genotoxicity of zebrafish Danio rerio for 24, 48, 72 and 96-hours acute exposure (level:1, 4, 16, 64 mg/l BA and BX) in semi-static bioassay experiment. For that purpose, peripheral erythrocytes were drawn from caudal vein and Comet assay was applied to assess genotoxicity. Acute (96 hours) exposure and high concentrations of boric acid and borax increases % tail DNA and Olive tail moment. Genotoxicity was found for BA as concentration-dependent and BX as concentration and time dependent manner. In general, significant effects (P borax-induced genotoxicity in fish.

  1. Model for conductometric detection of carbohydrates and alcohols as complexes with boric acid and borate ion in high-performance liquid chromatography

    International Nuclear Information System (INIS)

    Bertrand, G.L.; Armstrong, D.W.

    1989-01-01

    In recent articles, Okada has demonstrated the utility of indirect conductometric detection of electrically neutral sugars and alcohols through their complexes in boric acid solution. The use of a boric acid eluent provides a highly sensitive means of detection for monosaccharides, lactose, and sugar alcohols but not for polysaccharides (other than lactose) and simple alcohols. Addition of sorbitol, mannitol, or fructose to the boric acid eluent allows detection of the polysaccharides and simple alcohols, as well as lactose, glucose, fructose, and presumably other monosaccharides and sugar alcohols. These results were interpreted in terms of the ability of an analyte to form either dissociated or undissociated complexes with boric acid. This interpretation was quantified with a mathematical description of the complexation equilibria and the conductivity due to ionic species. Unfortunately, the mathematical model contains some incorrect assumptions that severely limit the utility of the derived equations and may prevent optimization of this potentially important technique. We present here a more general mathematical model that does not suffer from these limitations

  2. Synthesis of PBAD-lipiodol nanoparticles for combination treatment with boric acid in boron neutron capture therapy for hepatoma in-vitro

    International Nuclear Information System (INIS)

    Chou, F.I.; Chung, H.P.; Liu, H.M.; Wen, H.W.; Chi, C.W.; Lin, Shanyang; Lui, W.Y.; Kai, J.J.

    2006-01-01

    This study attempted to increase BNCT efficiency for hepatoma by a combined treatment of phenylboric acid derivative entrapped lipiodol nanoparticles (PBAD-L nanoparticles) with boric acid. The size of PBAD-L nanoparticles were 400-750 nm at the boron concentrations of 0.3-2.7 mg/ml. After 24 hours the boron concentration in PBAD-L nanoparticles treated human hepatoma HepG2 cells was 112 ppm, while that in rat liver Clone 9 cells was 52 ppm. With the use of 25 μg B/ml boric acid, after 6 hours the boron concentration in HepG2 and Clone 9 cells were 75 ppm and 40 ppm, respectively. In a combined treatment, boron concentration in HepG2 cells which were treated with PBAD-L nanoparticles for 18 hours and then combined with boric acid for 6 hours was 158 ppm. After neutron irradiation, the surviving fraction of HepG2 cells treated with PBAD-L nanoparticles was 12.6%, while that in the ones with a combined treatment was 1.3%. In conclusion, the combined treatment provided a higher boron concentration in HepG2 cells than treatments with either PBAD-L nanoparticles or boric acid, resulting in a higher therapeutic efficacy of BNCT in hepatoma cells. (author)

  3. Effect of complexing reagents on the ionization constant of boric acid and its relation to isotopic exchange separation factor

    International Nuclear Information System (INIS)

    Sharma, B.K.; Subramanian, R.; Mathur, P.K.

    1991-01-01

    The effect of change in concentration of complexing reagents having two or more hydroxyl groups, viz., ethylene glycol, propylene glycol, dextrose and mannitol on the ionization constant of boric acid has been studied by pH-metric titration method. The effect of increase in ionization constant of boric acid on isotopic exchange separation factor for the separation of isotopes of boron by ion exchange chromatography has been studied by the batch method. (author). 9 refs

  4. Hierarchical porous photoanode based on acid boric catalyzed sol for dye sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Maleki, Khatereh [School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, P.O. Box: 14395-553, Tehran (Iran, Islamic Republic of); Abdizadeh, Hossein [School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, P.O. Box: 14395-553, Tehran (Iran, Islamic Republic of); Center of Excellence for High Performance Materials, University of Tehran, Tehran (Iran, Islamic Republic of); Golobostanfard, Mohammad Reza, E-mail: Mohammadreza.Golbostanfard@gmail.com [School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, P.O. Box: 14395-553, Tehran (Iran, Islamic Republic of); Adelfar, Razieh [School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, P.O. Box: 14395-553, Tehran (Iran, Islamic Republic of)

    2017-02-01

    Highlights: • Acid boric can thoroughly leads to the hierarchical porous titania structure. • Boron is introduced into titania lattice which causes slight blueshift of bandgap. • The optimized sol parameters are H{sub 3}BO{sub 3}/TTiP = 0.45, DI/TTiP = 4.5, and 0.17 M. • Optimized paste parameters is not changed compared to conventional pastes. • The DSSC based on H{sub 3}BO{sub 3} catalyzed sol shows promising efficiency of 2.91%. - Abstract: The hierarchical porous photoanode of the dye sensitized solar cell (DSSC) is synthesized through non-aqueous sol-gel method based on H{sub 3}BO{sub 3} as an acid catalyst and the efficiencies of the fabricated DSSC based on these photoanodes are compared. The sol parameters of 0.17 M, water mole ratio of 4.5, acid mole ratio of 0.45, and solvent type of ethanol are introduced as optimum parameters for photoanode formation without any detectable cracks. The optimized hierarchical photoanode mainly contains anatase phase with slight shift toward higher angles, confirming the doping of boron into titania structure. Moreover, the porous structure involves two ranges of average pore sizes of 20 and 635 nm. The diffuse reflectance spectroscopy (DRS) shows the proper scattering and blueshift in band gap. The paste parameters of solid:liquid, TiO{sub 2}:ethyl cellulose, and terpineol:ethanol equal to 11:89, 3.5:7.5, and 25:64, respectively, are assigned as optimized parameters for this novel paste. The photovoltaic properties of short circuit current density, open circuit voltage, fill factor, and efficiency of 5.89 mA/cm{sup 2}, 703 mV, 0.7, and 2.91% are obtained for the optimized sample, respectively. The relatively higher short circuit current of the main sample compared to other samples is mainly due to higher dye adsorption in this sample corresponding to its higher surface area and presumably higher charge transfer confirmed by low R{sub S} and R{sub ct} in electrochemical impedance spectroscopy data. Boric acid as

  5. Estimation of influence of a solution of a boric acid and temperatures on a isolation material from basalt fibers

    International Nuclear Information System (INIS)

    Pyshnova, V.V.; Skobelkina, T.N.; Yurchenko, V.G.; Knot'ko, A.V.; Putlyaev, V.I.

    2006-01-01

    Paper presents the results of investigation into long-term simultaneous effect of a medium (boric acid solution) and temperature on a thermal-insulating basalt fiber material. The basalt fiber clothes used at the NPP were tested. When evaluating simultaneous effect of boric acid solution and temperature one kept watch on density, compressibility, elasticity and diameter of fiber. According to the results of 30 day tests, the basic technical parameters of the thermal-insulating material have changed insignificantly [ru

  6. Limitations when use chloramphenicol-bcyclodextrins complexes in ophtalmic solutions buffered with boric acid/borax system

    Directory of Open Access Journals (Sweden)

    Todoran Nicoleta

    2014-12-01

    Full Text Available Chloramphenicol eye drops are commonly prescribed in concentrations of 0.5-1% in the treatment of infectious conjunctivitis. In terms of ophthalmic solution preparation, the major disadvantage of chloramphenicol consists in its low solubility in water. The solubility is increased by substances that form chloramphenicol-complexes, for example: boric acid/borax or cyclodextrins. Objective: Experimental studies aimed to evaluate the potential advantages of enhancing the solubility and stability of chloramphenicol (API by molecular encapsulation in b-cyclodextrin (CD, in formulation of ophthalmic solutions buffered with boric acid/borax system. Methods and Results: We prepared four APIb- CD complexes, using two methods (kneading and co-precipitation and two molar ratio of API/b-cyclodextrin (1:1 and 1:2. The formation of complexes was proved by differential scanning calorimetry (DSC and the in vitro dissolution tests. Using these compounds, we prepared eight ophthalmic solutions, formulated in two variants of chloramphenicol concentrations (0.4% and 0.5%. Each solution was analyzed, by the official methods, at preparation and periodically during three months of storing in different temperature conditions (4°C, 20°C and 30°C. Conclusions: Inclusion of chloramphenicol in b-cyclodextrin only partially solves the difficulties due to the low solubility of chloramphenicol. The protection of chloramphenicol molecules is not completely ensured when the ophthalmic solutions are buffered with the boric acid/borax system.

  7. Boric acid as a mild and efficient catalyst for one-pot synthesis of 1

    Indian Academy of Sciences (India)

    Abstract. An efficient green chemistry method has been developed for the synthesis of 1-amidoalkyl-2-naphthol derivatives via a one-pot three-component condensation of 2-naphthol, aldehydes and amide in the presence of boric acid as a mild catalyst.

  8. The Usability of Boric Acid as an Alternative Foaming Agent on the Fabrication of Al/Al2O3 Composite Foams

    Science.gov (United States)

    Yaman, Bilge; Onuklu, Eren; Korpe, Nese O.

    2017-09-01

    Pure Al and alumina (2, 5, 10 wt.% Al2O3)-added Al composite foams were fabricated through powder metallurgy technique, where boric acid (H3BO3) is employed as a new alternative foaming agent. It is aimed to determine the effects of boric acid on the foaming behavior and cellular structure and also purposed to develop the mechanical properties of Al foams by addition of Al2O3. Al and Al composite foams with porosity fraction in the range of 46-53% were achieved by sintering at 620 °C for 2 h. Cell morphology was characterized using a combination of stereomicroscope equipped with image analyzer and scanning electron microscopy. Microhardness values were measured via using Vickers indentation technique. Quasi-static compression tests were performed at strain rate of 10-3 s-1. Compressive strength and energy absorption of the composite foams enhanced not only by the increasing weight fraction of alumina, but also by the usage of boric acid which leads to formation of boron oxide (B2O3) acting as a binder in obtaining dense cell walls. The results revealed that the boric acid has outstanding potential as foaming agent in the fabrication of Al and Al composite foams by providing improved mechanical properties.

  9. Effectiveness of 3 per cent boric acid in 70 per cent alcohol versus 1 per cent clotrimazole solution in otomycosis patients: a randomised, controlled trial.

    Science.gov (United States)

    Romsaithong, S; Tomanakan, K; Tangsawad, W; Thanaviratananich, S

    2016-09-01

    To compare the clinical effectiveness and adverse events for 3 per cent boric acid in 70 per cent alcohol versus 1 per cent clotrimazole solution in the treatment of otomycosis. A total of 120 otomycosis patients were randomly assigned to receive either 1 per cent clotrimazole solution (intervention group) or 3 per cent boric acid in 70 per cent alcohol (control group) at the Khon Kaen Hospital ENT out-patient department. Treatment effectiveness was determined based on the otomicroscopic absence of fungus one week after therapy, following a single application of treatment. After 1 week of treatment, there were data for 109 participants, 54 in the clotrimazole group and 55 in the boric acid group. The absolute difference in cure rates between 1 per cent clotrimazole solution and 3 per cent boric acid in 70 per cent alcohol was 17.9 per cent (95 per cent confidence interval, 2.3 to 33.5; p = 0.028) and the number needed to treat was 6 (95 per cent confidence interval, 3.0 to 43.4). Adverse events for the two agents were comparable. One per cent clotrimazole solution is more effective than 3 per cent boric acid in 70 per cent alcohol for otomycosis treatment.

  10. Determination of Optimum Duration and Concentration of Stevia (Stevia rebaudiana Bert.) Seed Priming with Boric Acid (H3BO3)

    OpenAIRE

    SHAHVERDI, Mehdi Aghighi; OMIDI, Heshmat; TABATABAEI, Seyed Jalal

    2017-01-01

    In order to determine optimal duration and concentration of Stevia seed priming with boric acid for improving germination, an experimental factorial completely randomized design with three replications was conducted in the laboratory of Seed Science and Technology, Shahed University of Tehran in 2015. The first factor was different concentrations of boric acid (0, 0.5, 1.0, 1.5 and 2.0 percent) and the second factor was priming duration (0, 8, 16, 24 and 32 hours). Effects of concentration an...

  11. Further investigation on boric acid catalytic graphitization of polyacrylonitrile carbon fibers: Mechanism and mechanical properties

    International Nuclear Information System (INIS)

    Wen, Ya; Lu, Yonggen; Xiao, Hao; Qin, Xianying

    2012-01-01

    Highlights: ► The modulus of carbon fiber was improved by boric acid at the temperature range of 1500–2900 °C. ► 2300 °C is a key temperature degree from which the boron began to benefit fiber strength. ► The fiber strength was affected by the boron reaction and related to the boron states. -- Abstract: Catalytic graphitization of polyacrylonitrile based carbon fibers by boric acid doping was studied and the dependence of fiber tensile strength on the boron content and temperature was discussed. It was found that there existed a key temperature point for the boron to take effect. When the fibers were modified with 7.0 wt.% boric acid solution, with increasing temperature, the tensile strength was lower than that of the unmodified ones below 2300 °C, but a reverse thing happened above 2300 °C. Moreover, when being heated at 2500 °C, the modified fibers showed an increasing tensile modulus and strength with increasing boron content till maximums of 404 GPa and 2.46 GPa, 26% and 16% higher than those of unmodified ones. The mechanical properties of the fibers were affected by the interaction of carbon and boron, and also related with boron states. The decomposition of boron acid and its interaction with carbon brought defects on fiber surface, degrading the mechanical properties below 1300 °C. With further heat treatment, the boron diffused into the fibers and divided into two states: substitutional and interstitial. At a temperature over 2300 °C with an appreciate boron content, the substitutional would be formed predominantly, which removed the structural defects and relaxed the distortions, so as to benefit the mechanical properties.

  12. Metal‐Free Dehydration of Glucose to 5‐(Hydroxymethyl)furfural in Ionic Liquids with Boric Acid as a Promoter

    DEFF Research Database (Denmark)

    Ståhlberg, Tim; Rodriguez, Sergio; Fristrup, Peter

    2011-01-01

    The dehydration of glucose and other hexose carbohydrates to 5‐(hydroxymethyl)furfural (HMF) was investigated in imidazolium‐based ionic liquids with boric acid as a promoter. A yield of up to 42 % from glucose and as much as 66 % from sucrose was obtained. The yield of HMF decreased as the conce......The dehydration of glucose and other hexose carbohydrates to 5‐(hydroxymethyl)furfural (HMF) was investigated in imidazolium‐based ionic liquids with boric acid as a promoter. A yield of up to 42 % from glucose and as much as 66 % from sucrose was obtained. The yield of HMF decreased...

  13. Cover Picture: Metal‐Free Dehydration of Glucose to 5‐(Hydroxymethyl)furfural in Ionic Liquids with Boric Acid as a Promoter (Chem. Eur. J. 5/2011)

    DEFF Research Database (Denmark)

    Ståhlberg, Tim Johannes Bjarki; Rodriguez, Sergio; Fristrup, Peter

    2011-01-01

    Boric acid promotes the dehydration of glucose to 5-(hydroxy)methylfurfural in ionic liquids. Computational analyses by DFT calculations show a significant decrease in energy for the isomerization of glucose to fructose when the sugars are bound to boric acid and isotopic labeling NMR studies con...

  14. Mechanism of Early Stage Corrosion for Boric-sulfuric Acid Anodized 2A97 Al-Cu-Li Alloy Under Tropical Marine Atmosphere

    Directory of Open Access Journals (Sweden)

    LUO Chen

    2016-09-01

    Full Text Available Optical microscopy(OM, scanning electron microscopy(SEM, EDX and EIS combined with ultramicrotomy were employed to investigate the micro morphology, chemical composition and electrochemical properties of anodized 2A97 Al-Cu-Li alloy before and after atmospheric corrosion. The results show that when electrolytes containing combinations of tartaric-sulfuric or boric-sulfuric acid are used to grow the films at different temperatures, boric acid addition and higher temperature allow for higher current density that speeds up the film growth. The pore geometry and structure is similar for different electrolytes. Dispersive dark rusty spots composed of O, Al, Cl, Cu are present on the boric-sulfuric acid anodized specimen after exposure in tropical marine atmosphere for 1 month. Deposition of white corrosion product is found on the specimen surface as well. Severe pitting occurs and develops deeply into the alloy substrate after elongated outdoor exposure. Corrosion propagation is associated with θ-phase particles.

  15. Design of Test Facility to Evaluate Boric Acid Precipitation Following a LOCA

    Energy Technology Data Exchange (ETDEWEB)

    Suh, Jeong-Kwan; Song, Yong-Jae [KHNP CRI, Daejeon (Korea, Republic of)

    2016-10-15

    The U.S.NRC has identified a concern that debris associated with generic safety issue (GSI) - 191 may affect the potential precipitation of boric acid due to one or more of the following phenomena: - Reducing mass transport (i.e. mixing) between the core and the lower plenum (should debris accumulate at the core inlet) - Reduced lower plenum volume (should debris settle in the lower plenum), and, - Increased potential for boric acid precipitation (BAP) in the core (should debris accumulate in suspension in the core) To address these BAP issues, KHNP is planning to conduct validation tests by constructing a BAP test facility. This paper describes the design of test facility to evaluate BAP following a LOCA. The design of BAP test facility has been developed by KHNP. To design the test facility, test requirements and success criteria were established, and scaling analysis of power-to-volume method, Ishii-Kataoka method, and hierarchical two-tiered method were investigated. The test section is composed of two fuel assemblies with half of full of prototypic FA height. All the fuel rods are heated by the electric power supplier. The BAP tests in the presence of debris, buffering agents, and boron will be performed following the test matrix.

  16. Evaluation of ultrasonic technique to characterize the concentration of boric acid in liquid medium; Avaliacao de tecnica ultrassonica para medida de concentracao de acido borico em meio liquido

    Energy Technology Data Exchange (ETDEWEB)

    Kohara, Richard Yuzo Ramida

    2015-06-01

    This dissertation is to analyze the viability of using ultrasonic technique to characterize the concentration of boric acid in liquid medium non-invasively, therefore, ultrasonic tests were performed relating different boric acid concentrations with the travel time of the ultrasonic wave, also were evaluated factors able to mask the characterization of these concentrations by ultrasonic technique. The results showed that the ultrasonic technique allows the characterization of boric acid concentrations in liquid medium in very simple terms by the ultrasonic wave travel time, requiring further studies in complex conditions. (author)

  17. 59Ni and 63Ni separation from boric acid concentrates produced at NPP

    International Nuclear Information System (INIS)

    Fisera, O.

    2010-01-01

    Procedure for direct separation of radionickel from boric acid concentrate was developed. Quantitative separation from 100 mL of real concentrate on the column filled with 3 mL of PAN-DMG composite material was achieved. PAN-DMG material (dimethylglyoxime in porous beads of polyacrylonitrile) was compared with Ni Resin and DMG-PAN material exhibited higher sorption capacity for nickel than Ni Resin. (author)

  18. Experimental Investigations to Enhance the Tribological Performance of Engine Oil by Using Nano-Boric Acid and Functionalized Multiwalled Carbon Nanotubes: A Comparative Study to Assess Wear in Bronze Alloy

    Science.gov (United States)

    Ajay Vardhaman, B. S.; Amarnath, M.; Ramkumar, J.; Rai, Prabhat K.

    2018-04-01

    In various mechanical systems, lubricants are generally used to reduce friction and wear; thus, the total energy loss in the mechanical systems can be minimized by the proper enhancement of lubrication properties. In general, friction modifiers and antiwear additives are used to improve the tribological properties of the lubricant. However, the use of these additives has to be phased out due to their fast chemical degradation in their applications and other environmental issues. In recent years, the use of nanoparticles as a potential lubricant additive has received considerable attention because of its excellent mechanical and tribological characteristics. The present work describes the tribological behavior of nano-boric acid, multiwalled carbon nanotubes (MWCNTs), and functionalized multiwalled carbon nanotubes (FMWCNTs) modified with carboxylic acid. These nanoparticles were used to enhance the tribological properties of engine oil (SAE20W40) used to lubricate bronze alloy samples. The performance of these nano-coolants was assessed on a linear reciprocating ball-on-flat tribometer. Results highlight the friction and wear behavior of the nano-boric acid, MWCNTs, and FMWCNTs under three varying parameters such as the effect of nanoparticles concentration, load-carrying capacity, and sliding speed. The addition of nano-boric acid, MWCNTs, and FMWCNTs has significantly improved the tribological properties of the base lubricant. The addition of 0.5 wt.% of nano-boric acid, MWCNTs, and FMWCNTs to the base lubricant has decreased the coefficient of friction by 19.76, 30.55, and 35.65%, respectively, and a significant reduction in wear volume by 55.17, 71.42, and 88.97% was obtained in comparison with base lubricant.

  19. Determination of boron as boric acid by automatic potentiometric titration

    International Nuclear Information System (INIS)

    Midgley, D.

    1988-06-01

    Boron in PWR primary coolant and related waters may be determined as boric acid by titration with sodium hydroxide, using a glass electrode as a pH indicator. With a modern automatic titrator, the analysis is quick, convenient, accurate and precise. In the titration of 8 mg B (e.g. 4 ml of 2000 mg 1 -1 solution), no significant bias was observed and relative standard deviations were about 0.25%. With 0.8 g B, a bias of about 2% appears, although this could be reduced by restandardizing the titrant, but the relative standard deviation was still -1 B, depending on the stage of the fuel cycle. (author)

  20. Boric acid as cost-effective and recyclable catalyst for trimethylsilyl protection and deprotection of alcohols and phenols

    Energy Technology Data Exchange (ETDEWEB)

    Rostami, Amin; Akradi, Jamal; Ahmad-Jangi, Firoz, E-mail: a_rostami372@yahoo.co [University of Kurdistan, Sanandaj (Iran, Islamic Republic of). Faculty of Science. Dept. of Chemistry

    2010-07-01

    Boric acid has been used as a green, selective and recyclable catalyst for trimethysilylation of alcohols and phenols using hexamethyldisilazane in acetonitrile. Deprotection of trimethylsilyl ethers to their parent alcohols and phenols was also achieved using this catalyst in water at room temperature. The salient features of this methodology are cheap processing, mild acidity conditions, excellent yields of products and easy availability of the catalyst. (author)

  1. Fiberboards treated with N’-N-(1, 8-Naphthalyl) hydroxylamine (NHA-Na), borax, and boric acid

    Science.gov (United States)

    Turgay Akbulut; S. Nami Kartal; Frederick Green

    2004-01-01

    This paper reports on the physical and mechanical properties and decay and termite resistance of fiberboard panels made from pine and beech treated with N’-N-(1, 8-Naphthalyl) hydroxylamine sodium salt(NHA-Na), borax, and boric acid at varying loadings. The panels were manufactured using 10 percent urea-formaldehyde resin and 1 percent NH4Cl. Mechanical and physical...

  2. Simultaneous pollutant removal and electricity generation in denitrifying microbial fuel cell with boric acid-borate buffer solution.

    Science.gov (United States)

    Chen, Gang; Zhang, Shaohui; Li, Meng; Wei, Yan

    2015-01-01

    A double-chamber denitrifying microbial fuel cell (MFC), using boric acid-borate buffer solution as an alternative to phosphate buffer solution, was set up to investigate the influence of buffer solution concentration, temperature and external resistance on electricity generation and pollutant removal efficiency. The result revealed that the denitrifying MFC with boric acid-borate buffer solution was successfully started up in 51 days, with a stable cell voltage of 205.1 ± 1.96 mV at an external resistance of 50 Ω. Higher concentration of buffer solution favored nitrogen removal and electricity generation. The maximum power density of 8.27 W/m(3) net cathodic chamber was obtained at a buffer solution concentration of 100 mmol/L. An increase in temperature benefitted electricity generation and nitrogen removal. A suitable temperature for this denitrifying MFC was suggested to be 25 °C. Decreasing the external resistance favored nitrogen removal and organic matter consumption by exoelectrogens.

  3. The Effect of Boric Acid and Borax on Oxidative Stress, Inflammation, ER Stress and Apoptosis in Cisplatin Toxication and Nephrotoxicity Developing as a Result of Toxication.

    Science.gov (United States)

    Hazman, Ömer; Bozkurt, Mehmet Fatih; Fidan, Abdurrahman Fatih; Uysal, Fadime Erkan; Çelik, Sefa

    2018-03-02

    The development of treatment protocols that can reduce side effects in chemotherapy applications is extremely important in terms of cancer treatment. In this context, it was aimed to investigate the effects of boric acid and borax on cisplatin toxicity (nephrotoxicity) in rats. In the experimental phase, eight groups were formed from rats. Boric acid and borax were given to the treatment groups with three different doses using gavage. On the fifth day of the study, cisplatin (10 mg/kg) was administered to all rats except the control group. At the end of the study, oxidative stress-related (GSH, MDA, PCO, GPx, 8-OHdG), inflammation-related (TNF-α, IL-1β, IL-18, MCP-1, ICAM, TGF-β), apoptosis-related (p53, caspase 1, 3, 8, 12, bcl-2, bcl-xL, NFkB), and ER stress-related (GRP78, ATF-6, PERK) basic parameters were analyzed in serum, erythrocyte, and kidney tissues. Kidney tissues were also examined by histopathological and immunohistochemical methods. Borax and boric acid at different doses decreased inflammation and oxidative stress caused by cisplatin toxicity and increased ER stress. As a result of the treatments applied to experimental animals, it was determined that boric acid and borax reduced apoptotic damage in kidney tissue, but the decrease was statistically significant only in 200 mg/kg boric acid-administered group. In the study, low anti-apoptotic effects of borate doses with the anti-inflammatory and antioxidant effect may be due to increased ER stress at the relevant doses. Further studies on the effects of boron compounds on ER stress and apoptotic mechanisms may clarify this issue. Thus, possible side effects or if there are new usage areas of borone compounds which have many usage areas in clinics can be detected.

  4. EFFECTS.OF BORIC ACID ON THE CURE OF BORON-FILLED Y-3602 SILICONE GUM

    Energy Technology Data Exchange (ETDEWEB)

    Leichliter, G E

    1974-10-01

    The first two phases of a program designed to determine the effects of boric acid on the cure of Y-3602 silicone gum were conducted to evaluate extraction solvents and extraction time. The standard production formulation of B10-filled Y-3602 silicone gum was used in these evaluations. Results showed that the best solvent for reproducibility and high amine content was chloroform. The second phase indicated that extraction was essentially complete at the end of 4 hours.

  5. Limitations when use chloramphenicol-bcyclodextrins complexes in ophtalmic solutions buffered with boric acid/borax system

    OpenAIRE

    Todoran Nicoleta; Ciurba Adriana; Rédai Emőke; Ion V.; Lazăr Luminița; Sipos Emese

    2014-01-01

    Chloramphenicol eye drops are commonly prescribed in concentrations of 0.5-1% in the treatment of infectious conjunctivitis. In terms of ophthalmic solution preparation, the major disadvantage of chloramphenicol consists in its low solubility in water. The solubility is increased by substances that form chloramphenicol-complexes, for example: boric acid/borax or cyclodextrins. Objective: Experimental studies aimed to evaluate the potential advantages of enhancing the solubility and stability ...

  6. Boric Acid as an Accelerator of Cerium Surface Treatment on Aluminum

    Directory of Open Access Journals (Sweden)

    K. Cruz-Hernández

    2014-01-01

    Full Text Available Aluminum pieces are often used in various industrial processes like automotive and aerospace manufacturing, as well as in ornamental applications, so it is necessary to develop processes to protect these materials, processes that can be industrialized to protect the aluminum as well or better than chromate treatments. The purpose of this research is to evaluate boric acid as an accelerator by optimizing its concentration in cerium conversion coatings (CeCC with 10-minute immersion time with a concentration of 0.1 g L−1 over aluminum to protect it. The evaluation will be carried out by measuring anticorrosion properties with electrochemical techniques (polarization resistance, Rp, polarization curves, PC, and electrochemical impedance spectroscopy, EIS in NaCl 3.5% wt. aqueous solution and surface characterization with scanning electron microscopy (SEM.

  7. Effects of sublethal exposure to boric acid sugar bait on adult survival, host-seeking, bloodfeeding behavior, and reproduction of Stegomyia albopicta.

    Science.gov (United States)

    Ali, Arshad; Xue, Rui-De; Barnard, Donald R

    2006-09-01

    Effects of sublethal exposure to 0.1% boric acid sugar bait on adult survival, host-seeking, bloodfeeding behavior, and reproduction of Stegomyia albopicta were studied in the laboratory. Survival of males as well as females was significantly reduced when exposed to the bait, compared to control adults. The host-seeking and bloodfeeding activities in the baited females decreased, but the mean duration of blood engorgement (probing to voluntary withdrawal of proboscis) was not significantly different between the baited and control females. The landing and biting rates (human forearm) were significantly reduced in the baited females compared to nonbaited controls. Fecundity and fertility (based on number of laid eggs per female and percentage egg hatch, respectively) in the baited females were significantly reduced, and ovarian development was retarded. Sublethal exposure to sugar-based boric acid bait has the potential to reduce adult populations of St. albopicta.

  8. Effect of boric acid composition on the properties of ZnO thin film nanotubes and the performance of dye-sensitized solar cell (DSSC)

    Energy Technology Data Exchange (ETDEWEB)

    Rahman, M.Y.A., E-mail: mohd.yusri@ukm.edu.my; Roza, L.; Umar, A.A., E-mail: akrajas@ukm.edu.my; Salleh, M.M.

    2015-11-05

    The effect of boric acid (H{sub 3}BO{sub 3}) composition at constant concentration of hexamethylenetetramine (HMT) and zinc nitrate (Zn(NO{sub 3}){sub 2}) on the morphology, thickness, elemental composition, optical absorption, structure, photoluminescence of ZnO nanotubes has been investigated. The performance of the DSSC utilizing the ZnO samples has also been studied. It was found that the structure, thickness, elemental composition, optical absorption and morphology of ZnO nanostructure are significantly affected by the concentration of H{sub 3}BO{sub 3}. The diameter and thickness of ZnO nanotubes decreases as the composition of H{sub 3}BO{sub 3} increases. The DSSC utilizing ZnO nanotubes synthesized at 2 wt. % H{sub 3}BO{sub 3} performs the highest J{sub SC} and η of 2.67 mA cm{sup −2} and 0.29%, respectively. The highest performance of the device is due to the highest optical absorption of ZnO nanotubes sample and lowest charge interfacial resistance. - Graphical abstract: Nyquist plots of the DSSCs utilizing ZnO nanotubes prepared at various boric acid compositions. - Highlights: • Boron was doped into ZnO films by adding H{sub 3}BO{sub 3} into the growth solution. • Diameter and thickness of ZnO nanotubes decreases with the composition of H{sub 3}BO{sub 3}. • The DSSC performs the highest J{sub SC} and η of 2.67 mA cm{sup −2} and 0.29%, respectively. • This is due to high specific surface area and low charge interfacial resistance.

  9. An assessment of boric acid and borax using the IEHR Evaluative Process for Assessing Human Developmental and Reproductive Toxicity of Agents. Expert Scientific Committee.

    Science.gov (United States)

    Moore, J A

    1997-01-01

    Boron is a ubiquitous element widely distributed in nature in the form of borates at low concentrations in soils and rocks. Boron is released from these minerals by the natural weathering processes in the form of boric acid, which is water soluble and biologically available. High levels of boric acid are naturally found in sea water. Boric acid and borax are used in the greatest quantities and represent the major boron chemical exposures to humans and the environment. The principal use of boric acid and borax is in the manufacture of various types of glass products that do not result in exposure to the consumer. Boric acid and borax are also found in an array of consumer goods including fireproofing for fabrics and wood, insecticides, and in many cosmetics and personal care products as well. Boron may be an essential element for higher animals including humans. Boric acid and borax are considered to be completely absorbed by the oral route of exposure. Absorption through intact skin is considered negligible, although absorption can occur through denuded or irritated skin. Boron levels in the body do not persist upon cessation of exposure. People may be exposed to boron through three primary sources: 1) consumption of private, municipal, or commercial (bottled) sources of drinking water; 2) dietary consumption of crops and other foodstuffs (including dietary supplements for body building); and 3) inhalation of boron compounds during their mining, manufacturing, and other industrial processing. While boron has been detected in 81.8% of the municipal water systems, it is a minor source of boron in most parts of the U.S. The mean boron concentration is reported as 0.2 mg B/L. However, residents of California and other western states with boron-rich geologic deposits may be regularly exposed to higher levels in drinking water. Individuals who drink bottled mineral water may also increase their exposure to boron. An EPA health advisory, recommends boron concentrations in

  10. Effects of Induction Heat Bending and Heat Treatment on the Boric Acid Corrosion of Low Alloy Steel Pipe for Nuclear Power Plants

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Ki-Tae; Kim, Young-Sik [Andong National University, Gyeongbuk (Korea, Republic of); Chang, Hyun-Young; Park, Heung-Bae [KEPCO EandC, Gyeongbuk (Korea, Republic of); Sung, Gi-Ho; Shin, Min-Chul [Sungil SIM Co. Ltd, Busan (Korea, Republic of)

    2016-11-15

    In many plants, including nuclear power plants, pipelines are composed of numerous fittings such as elbows. When plants use these fittings, welding points need to be increased, and the number of inspections also then increases. As an alternative to welding, the pipe bending process forms bent pipe by applying strain at low or high temperatures. This work investigates how heat treatment affects on the boric acid corrosion of ASME SA335 Gr. P22 caused by the induction heat bending process. Microstructure analysis and immersion corrosion tests were performed. It was shown that every area of the induction heat bent pipe exhibited a high corrosion rate in the boric acid corrosion test. This behavior was due to the enrichment of phosphorous in the ferrite phase, which occurred during the induction heat bending process. This caused the ferrite phase to act as a corrosion initiation site. However, when re-heat treatment was applied after the bending process, it enhanced corrosion resistance. It was proved that this resistance was closely related to the degree of the phosphorus segregation in the ferrite phase.

  11. Update of the water chemistry effect on the flow-accelerated corrosion rate of carbon steel: influence of hydrazine, boric acid, ammonia, morpholine and ethanolamine

    International Nuclear Information System (INIS)

    Pavageau, E.-M.; De Bouvier, O.; Trevin, S.; Bretelle, J.-L.; Dejoux, L.

    2007-01-01

    The influence of the water chemistry on Flow-Accelerated Corrosion (FAC) affecting carbon steel components has been studied for many years and is relatively well known and taken into account by the models. Nonetheless, experimental studies were conducted in the last few years at EDF on the CIROCO loop in order to check the influence of the water chemistry parameters (hydrazine, boric acid, ammonia, morpholine and ethanolamine) on the FAC rate of carbon steel in one phase flow conditions. The hydrazine impact on the FAC rate was shown to be minor in EDF's chemistry recommendation range, compared to other parameters' effects such as the pH effect. The presence of boric acid in the nominal secondary circuit conditions was negligible. Finally, as expected, the nature of the chemical conditioning (ammonia, morpholine or ethanolamine) did not modify the FAC rate, the influencing chemical variable being the at-temperature pH in one-phase flow conditions. (author)

  12. The Effects of Foliar Application of Urea, Calcium Nitrate and Boric Acid on Growth and Yield of Greenhouse Cucumber (cv. Khassib

    Directory of Open Access Journals (Sweden)

    Naser Nasrolahzadehasl

    2017-10-01

    Full Text Available Introduction: Cucumis sativus L. is one of the most eminent and consuming vegetables which is widely cultivated in the Middle East. Using the controlled and greenhouse cultivation is one of the most appropriate methods to increase production per unit area. In this method, controlling the effective factors of production such as plant nutrition is the important factor to achieve high performance. Besides the accuracy applied in nutritional regulation of plant roots (both in soil and hypothermic environments, in many cases, foliar nutrition is considered by breeder of greenhouse productions. Foliar nutrition is more effective on young leaves, and deficiency of macro and micro nutrients can be removed by this factor. Khassib is one of the most important cultivar of greenhouse cucumber which is widely cultivated in Iran. The present study was conducted to evaluate the effect of foliar application on greenhouse cucumber. Materials and Methods: The experiment was performed on greenhouse cucumber (cv. Khassib for five months (from March 2007 to July 2008 in Ziba Dasht Technical Instruction Center which is located near Karaj, Iran. For this reason the experiment was conducted based on split-split-plot design with three replications. Eight experimental treatments were applied for foliar application including U1C1B1: urea + calcium nitrate +boric acid, U1C1B0: urea + calcium nitrate, U1C0B1: urea + boric acid, U1C0B0: urea, U0C1B1: calcium nitrate + boric acid, U0C1B0: calcium nitrate, U0C0B1: boric acid, U0C0B0: control. The effects of urea, calcium nitrate and boric acid in concentrations 3, 10 and 0.5 (gL-1 respectively on qualitative and quantitative characteristics of greenhouse cucumber, including fruit yield, yield of first class fruit, number of fruits, percentage of first class fruit, fruits T.S.S, plant length, percentage of leaf dry matter, and leaf weight ratio were studied. Results and Discussion: The results showed that calcium nitrate had a

  13. Fabrication of Li{sub 2}TiO{sub 3} pebbles using PVA–boric acid reaction for solid breeding materials

    Energy Technology Data Exchange (ETDEWEB)

    Park, Yi-Hyun, E-mail: yhpark@nfri.re.kr; Cho, Seungyon; Ahn, Mu-Young

    2014-12-15

    Highlights: • Li{sub 2}TiO{sub 3} pebbles were successfully fabricated by the slurry droplet wetting method. • Boron was used as hardening agent of PVA and completely removed during sintering. • Microstructure of fabricated Li{sub 2}TiO{sub 3} pebble was exceptionally homogeneous. • Suitable process conditions for high-quality Li{sub 2}TiO{sub 3} pebble were summarized. - Abstract: Lithium metatitanate (Li{sub 2}TiO{sub 3}) is a candidate breeding material of the Helium Cooled Ceramic Reflector (HCCR) Test Blanket Module (TBM). The breeding material is used in pebble-bed form to reduce the uncertainty of the interface thermal conductance. In this study, Li{sub 2}TiO{sub 3} pebbles were successfully fabricated by the slurry droplet wetting method using the cross-linking reaction between polyvinyl alcohol (PVA) and boric acid. The effects of fabrication parameters on the shaping of Li{sub 2}TiO{sub 3} green body were investigated. In addition, the basic characteristics of the sintered pebble were also evaluated. The shape of Li{sub 2}TiO{sub 3} green bodies was affected by slurry viscosity, PVA content and boric acid content. The grain size and average crush load of sintered Li{sub 2}TiO{sub 3} pebble were controlled by the sintering time. The boron was completely removed during the final sintering process.

  14. The effects of dietary boric acid and borax supplementation on lipid peroxidation, antioxidant activity, and DNA damage in rats.

    Science.gov (United States)

    Ince, Sinan; Kucukkurt, Ismail; Cigerci, Ibrahim Hakki; Fatih Fidan, A; Eryavuz, Abdullah

    2010-07-01

    The aims of this study were to clarify the effects of high dietary supplementation with boric acid and borax, called boron (B) compounds, on lipid peroxidation (LPO), antioxidant activity, some vitamin levels, and DNA damage in rats. Thirty Sprague Dawley male rats were divided into three equal groups: the animals in the first group (control) were fed with a standard rodent diet containing 6.4 mg B/kg, and the animals in the experimental group were fed with a standard rodent diet added with a supra-nutritional amount of boric acid and borax (100 mg B/kg) throughout the experimental period of 28 days. The B compounds decreased malondialdehyde (MDA), DNA damage, the protein carbonyl content (PCO) level in blood, and glutathione (GSH) concentration in the liver, Cu-Zn superoxide dismutase (SOD), and catalase (CAT) activity in the kidney. The B compounds increased GSH concentration in blood and the vitamin C level in plasma. Consequently, our results demonstrate that B supplementation (100 mg/kg) in diet decreases LPO, and enhances the antioxidant defense mechanism and vitamin status. There are no differences in oxidant/antioxidant balance and biochemical parameters except for serum vitamin A and liver GSH concentration, between the boron compounds used in this study. Crown Copyright 2010. Published by Elsevier GmbH. All rights reserved.

  15. The use of Zeolite into the controlling of Lithium concentration in the PWR primary water coolant (I) : the influences of Ca, Mg and Boric Acid concentration into the exchanges capacity of Ammonium Zeolite

    International Nuclear Information System (INIS)

    Sumijanto; Siti-Amini

    1996-01-01

    In this first part of research, the influences of calsium, magnesium and boric acid concentrations to the zeolite uptake of lithium in the PWR primary water coolant have been studied. The ammonium form of zeolite was found by modification of the natural zeolite which was originated from Bayah. The results showed that the boric acid concentration in the normal condition of PWR operation absolutely did not affects the lithium uptake. The Li uptake efficiency was influenced by the presence of Ca and Mg ions in order to the presence of cations competition which was dominated by Ca ion

  16. In vivo percutaneous absorption of boric acid, borax, and disodium octaborate tetrahydrate in humans compared to in vitro absorption in human skin from infinite and finite doses.

    Science.gov (United States)

    Wester, R C; Hui, X; Hartway, T; Maibach, H I; Bell, K; Schell, M J; Northington, D J; Strong, P; Culver, B D

    1998-09-01

    Literature from the first half of this century report concern for toxicity from topical use of boric acid, but assessment of percutaneous absorption has been impaired by lack of analytical sensitivity. Analytical methods in this study included inductively coupled plasma-mass spectrometry which now allows quantitation of percutaneous absorption of 10B in 10B-enriched boric acid, borax, and disodium octaborate tetrahydrate (DOT) in biological matrices. This made it possible, in the presence of comparatively large natural dietary boron intakes for the in vivo segment of this study, to quantify the boron passing through skin. Human volunteers were dosed with 10B-enriched boric acid, 5.0%, borax, 5.0%, or disodium octaborate tetrahydrate, 10%, in aqueous solutions. Urinalysis, for boron and changes in boron isotope ratios, was used to measure absorption. Boric acid in vivo percutaneous absorption was 0.226 (SD = 0.125) mean percentage dose, with flux and permeability constant (Kp) calculated at 0.009 microgram/cm2/h and 1.9 x 10(-7) cm/h, respectively. Borax absorption was 0.210 (SD = 0.194) mean percentage of dose, with flux and Kp calculated at 0.009 microgram/cm2/h and 1.8 x 10(-7) cm/h, respectively. DOT absorption was 0.122 (SD = 0.108) mean percentage, with flux and Kp calculated at 0.01 microgram/cm2/h and 1.0 x 10(-7) cm/h, respectively. Pretreatment with the potential skin irritant 2% sodium lauryl sulfate had no effect on boron skin absorption. In vitro human skin percentage of doses of boric acid absorbed were 1.2 for a 0.05% solution, 0.28 for a 0.5% solution, and 0.70 for a 5.0% solution. These absorption amounts translated into flux values of, respectively, 0.25, 0.58, and 14.58 micrograms/cm2/h and permeability constants (Kp) of 5.0 x 10(-4), 1.2 x 10(-4), and 2.9 x 10(-4) cm/h for the 0.05, 0.5, and 5.0% solutions. The above in vitro doses were at infinite, 1000 microliters/cm2 volume. At 2 microliters/cm2 (the in vivo dosing volume), flux decreased some

  17. Synthesis of 1-amidoalkyl-2-naphthols based on a three-component reaction catalyzed by boric acid as a solid heterogeneous catalyst under solvent-free conditions

    Directory of Open Access Journals (Sweden)

    Zahed Karimi-Jaberi

    2012-12-01

    Full Text Available An efficient method for the preparation of 1-amidoalkyl-2-naphthols has been described using a multi-component, one-pot condensation reaction of 2-naphthol, aldehydes and amides in the presence of boric acid under solvent-free conditions.DOI: http://dx.doi.org/10.4314/bcse.v26i3.18

  18. Reconstitution of Vanadium Haloperoxidase's Catalytic Activity by Boric Acid-Towards a Potential Biocatalytic Role of Boron.

    Science.gov (United States)

    Natalio, Filipe; Wiese, Stefanie; Brandt, Wolfgang; Wessjohann, Ludger

    2017-04-11

    Boron's unusual properties inspired major advances in chemistry. In nature, the existence and importance of boron has been fairly explored (e.g. bacterial signaling, plant development) but its role as biological catalyst was never reported. Here, we show that boric acid [B(OH) 3 ] can restore chloroperoxidase activity of Curvularia inaequalis recombinant apo-haloperoxidase's (HPO) in the presence of hydrogen peroxide and chloride ions. Molecular modeling and semi-empirical PM7 calculations support a thermodynamically highly favored (bio)catalytic mechanism similarly to vanadium haloperoxidases (V-HPO) in which [B(OH) 3 ] is assumedly located in apo-HPO's active site and a monoperoxyborate [B(OH) 3 (OOH) - ] intermediate is formed and stabilized by interaction with specific active site amino acids leading ultimately to the formation of HOCl. Thus, B(OH) 3 -HPO provides the first evidence towards the future exploitation of boron's role in biological systems. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Effects on concrete from borated water and boric compounds cast into the concrete

    International Nuclear Information System (INIS)

    Fagerlund, Goeran

    2010-06-01

    A study has been made of the effects on concrete of its exposure to external water containing boric acid, and the effects on concrete of boric compounds cast into the concrete during its manufacture. According to information in literature boric acid is a weak Lewis acid that has no effect on concrete. Reaction between calcium hydroxide existing in concrete and boric acid might occur at the concrete surface. The reaction product formed (calcium-metaboritehexahydrate) has lower solubility than calcium hydroxide itself. Therefore, the reaction is reasonably harmless. Accelerated and non-accelerated test methods exist by which quantitative information on the effect of boric acid can be obtained. The test principles are described. Boron-containing compounds might be mixed into concrete in order to increase its resistance to neutron radiation. Pure boron minerals, as well as boron-containing residual materials from processing of natural boron minerals, might be used. Concrete might be affected with regard to the following properties: - Workability of the fresh concrete; - Stiffening and hardening of the concrete; - Strength (compression, tension); - Deformation (E-modulus, creep); - Durability (chemical, steel corrosion. Information in literature indicates that the hardening process might be severely affected also when rather small amounts of certain boron-containing materials are used. The effect seems to be small, or none, however, if materials with low solubility are used. The effect on workability seems to be marginal. Test methods exist by which it is practical possible to develop acceptable concrete recipes. The effects on mechanical properties are not well clarified by research. However, effects seem to be small when boron materials with low solubility are used. In one study, in which part of the cement was replaced by a boron containing colemanite waste, it was found that the E-modulus was very much reduced. The significance of this result is unclear. The

  20. Interaction of sodium monoborate and boric acid with some mono- and disaccharides in aqueous solutions (from data on isomolar solutions method)

    International Nuclear Information System (INIS)

    Shvarts, E.M.; Ignash, R.T.; Belousova, R.G.

    2000-01-01

    Interaction of sodium monoborate Na[B(OH) 4 ] and boric acid with D-glucose, D-fructose, D-saccharose and D-lactose in aqueous solution depending on the solution total concentration is studied through the method of isomolar solutions with application of conductometry and polarimetry. It is shown by the D-glucose and D-fructose examples that the method of isomolar solutions leads to results compatible with the data obtained by other methods and it may be applied to other saccharides [ru

  1. Method for the reprocessing of liquid wastes containing boric acid, radioactive antimony and other radioactive nuclides and similar, especially of the evaporator concentrates of nuclear power plants

    International Nuclear Information System (INIS)

    Doerr, A.

    1978-01-01

    The liquid wastes are evaporated, H 2 SO 4 and methanol are added, and the formed boric acid methylester is distilled off. The residue with Sb-124, Cs, Co and Mn is then stored two years until the activity of Sb-124 has decayed. Afterwards the radioactive nuclides are precipitated. (DG) [de

  2. Boric/sulfuric acid anodizing of aluminum alloys 2024 and 7075: Film growth and corrosion resistance

    Energy Technology Data Exchange (ETDEWEB)

    Thompson, G.E.; Zhang, L.; Smith, C.J.E.; Skeldon, P.

    1999-11-01

    The influence of boric acid (H{sub 3}BO{sub 3}) additions to sulfuric acid (H{sub 2}SO{sub 4}) were examined for the anodizing of Al 2024-T3 (UNS A92024) and Al 7075-T6 (UNS A97075) alloys at constant voltage. Alloys were pretreated by electropolishing, by sodium dichromate (Na{sub 2}Cr{sub 2}O{sub 7})/H{sub 2}SO{sub 4} (CSA) etching, or by alkaline etching. Current-time responses revealed insignificant dependence on the concentration of H{sub 3}BO{sub 3} to 50 g/L. Pretreatments affected the initial film development prior to the establishment of the steady-state morphology of the porous film, which was related to the different compositions and morphologies of pretreated surfaces. More detailed studies of the Al 7075-T6 alloy indicated negligible effects of H{sub 3}BO{sub 3} on the coating weight, morphology of the anodic film, and thickening rate of the film, or corrosion resistance provided by the film. In salt spray tests, unsealed films formed in H{sub 2}SO{sub 4} or mixed acid yielded similar poor corrosion resistances, which were inferior to that provided by anodizing in chromic acid (H{sub 2}CrO{sub 4}). Sealing of films in deionized water, or preferably in chromate solution, improved corrosion resistance, although not matching the far superior performance provided by H{sub 2}CrO{sub 4} anodizing and sealing.

  3. [Progress in sample preparation and analytical methods for trace polar small molecules in complex samples].

    Science.gov (United States)

    Zhang, Qianchun; Luo, Xialin; Li, Gongke; Xiao, Xiaohua

    2015-09-01

    Small polar molecules such as nucleosides, amines, amino acids are important analytes in biological, food, environmental, and other fields. It is necessary to develop efficient sample preparation and sensitive analytical methods for rapid analysis of these polar small molecules in complex matrices. Some typical materials in sample preparation, including silica, polymer, carbon, boric acid and so on, are introduced in this paper. Meanwhile, the applications and developments of analytical methods of polar small molecules, such as reversed-phase liquid chromatography, hydrophilic interaction chromatography, etc., are also reviewed.

  4. Results Of Analytical Sample Crosschecks For Next Generation Solvent Extraction Samples Isopar L Concentration And pH

    International Nuclear Information System (INIS)

    Peters, T.; Fink, S.

    2011-01-01

    As part of the implementation process for the Next Generation Cesium Extraction Solvent (NGCS), SRNL and F/H Lab performed a series of analytical cross-checks to ensure that the components in the NGCS solvent system do not constitute an undue analytical challenge. For measurement of entrained Isopar(reg s ign) L in aqueous solutions, both labs performed similarly with results more reliable at higher concentrations (near 50 mg/L). Low bias occurred in both labs, as seen previously for comparable blind studies for the baseline solvent system. SRNL recommends consideration to use of Teflon(trademark) caps on all sample containers used for this purpose. For pH measurements, the labs showed reasonable agreement but considerable positive bias for dilute boric acid solutions. SRNL recommends consideration of using an alternate analytical method for qualification of boric acid concentrations.

  5. Influences of boric acid and lithium hydroxide on oxide film of type 316 stainless steel in PWR simulated primary water; PWR 1次冷却材模擬環境中の316ステンレス鋼に生成した皮膜性状に及ぼすほう酸および水酸化リチウムの影響

    Energy Technology Data Exchange (ETDEWEB)

    Fukumura, Takuya; Fukuya, Koji; Arioka, Koji [Institute of Nuclear Safety System, Inc., Mihama, Fukui (Japan)

    2012-06-15

    In order to understand the influences of boric acid and lithium hydroxide on the IGSCC of type 316 stainless steel, an oxide film was analyzed in simulated PWR primary water while varying the boric acid and lithium hydroxide concentrations. It was found that, although boric acid and lithium hydroxide did not affect the structure and chemical composition of the surface oxide film remarkably, a lower boric acid concentration or a higher lithium concentration produced an oxide film with a thicker surface. It was considered that the lower boric acid concentration and higher lithium hydroxide concentration caused a higher magnetite solubility at the surface of the material and that the higher magnetite solubility caused a higher iron concentration gradient, which promoted iron dissolution from the material and the formation of a thicker oxide film. It was found that the thicker oxide film caused a higher IGSCC susceptibility and that the corrosion was the dominant factor of the IGSCC mechanism. No significant change was found in the morphologies of crack tip oxide in different bulk water chemistry systems, thus producing CT specimens with similar crack growth rates. (author)

  6. Stability of Hydrogen-Bonded Supramolecular Architecture under High Pressure Conditions: Pressure-Induced Amorphization in Melamine-Boric Acid Adduct

    International Nuclear Information System (INIS)

    Wang, K.; Duan, D.; Wang, R.; Lin, A.; Cui, Q.; Liu, B.; Cui, T.; Zou, B.; Zhang, X.

    2009-01-01

    The effects of high pressure on the structural stability of the melamine-boric acid adduct (C3N6H6 2H3BO3, M 2B), a three-dimensional hydrogen-bonded supramolecular architecture, were studied by in situ synchrotron X-ray diffraction (XRD) and Raman spectroscopy. M 2B exhibited a high compressibility and a strong anisotropic compression, which can be explained by the layerlike crystal packing. Furthermore, evolution of XRD patterns and Raman spectra indicated that the M 2B crystal undergoes a reversible pressure-induced amorphization (PIA) at 18 GPa. The mechanism for the PIA was attributed to the competition between close packing and long-range order. Ab initio calculations were also performed to account for the behavior of hydrogen bonding under high pressure.

  7. Determination of boron as boric acid by automatic potentiometric titration using Gran plots [in pressurized water reactor coolant

    International Nuclear Information System (INIS)

    Midgley, D.; Gatford, C.

    1989-11-01

    Boron in PWR primary coolant and related waters may be determined as boric acid by titration with sodium hydroxide, using a glass electrode as a pH indicator. Earlier work has shown that this analysis can conveniently be carried out automatically with adequate precision and accuracy for routine use, although bias became apparent at the lowest concentrations tested. The latest titrators enable the titration data to be transformed mathematically to give two linear segments, before and after the end-point (Gran plots). The results are as precise as those from other titration methods (in which the end-point is found from the point of inflexion of a plot of pH against volume of titrant), but the bias at low concentrations is much reduced. This is achieved without extra time or involvement of the operator. (author)

  8. Boric Ester-Type Molten Salt via Dehydrocoupling Reaction

    Directory of Open Access Journals (Sweden)

    Noriyoshi Matsumi

    2014-11-01

    Full Text Available Novel boric ester-type molten salt was prepared using 1-(2-hydroxyethyl-3-methylimidazolium chloride as a key starting material. After an ion exchange reaction of 1-(2-hydroxyethyl-3-methylimidazolium chloride with lithium (bis-(trifluoromethanesulfonyl imide (LiNTf2, the resulting 1-(2-hydroxyethyl-3-methylimidazolium NTf2 was reacted with 9-borabicyclo[3.3.1]nonane (9-BBN to give the desired boric ester-type molten salt in a moderate yield. The structure of the boric ester-type molten salt was supported by 1H-, 13C-, 11B- and 19F-NMR spectra. In the presence of two different kinds of lithium salts, the matrices showed an ionic conductivity in the range of 1.1 × 10−4–1.6 × 10−5 S cm−1 at 51 °C. This was higher than other organoboron molten salts ever reported.

  9. Toxicological studies on the Use of acid applied or combined with gamma radiation for controlling the mediterranean fruit fly Ceratitis Capitata Wied

    International Nuclear Information System (INIS)

    Fadel, A.M.; Othman, K.S.A.

    1997-01-01

    Biological studies were conducted to determine the effect of boric acid applied alone to different stages of ceratitis capitata or combined with gamma radiation of the produced treated pupae (9 days old). At a concentration range of 200-2000 ppm of boric acid per gm larval diet, larval and pupal durations were insignificantly affected. Pupation significantly decreased with increasing concentration, and adult emergence significantly increased at higher concentrations. Lc50 value of boric acid applied to the larval diet was 250 ppm. Applying boric acid as a powder mixed with pupal medium, the Lc50 was 96 mg/gm sand. Male and emergence significantly decreased. Significant mortality was obtained in adults of C capitata after applying boric acid as a thin film on the inner surface of the experimental cages where the adults were kept or when mixed with their food or as powder on the cage bottom. Applying boric acid to larval diet and gamma radiation to the produced pupae (9 days old) insignificantly affected larval and durations, percent pupation, adult emergence or adult survival. In cross-mating experiments, egg hatch ability was significantly reduced in the combination treatments of boric acid (500, 1000 ppm) and gamma radiation (90 Gy). On the other hand gamma radiation combined with boric acid treatments significantly increased male mating competitiveness at the concentration of 1000 ppm of boric acid followed by gamma irradiation (90 Gy). 2 figs., 5 tabs

  10. Importance of temperature, pH, and boric acid concentration on rates of hydrogen production from galvanized steel corrosion

    International Nuclear Information System (INIS)

    Loyola, V.M.

    1982-01-01

    One of the known sources of hydrogen gas within a nuclear plant containment building during a LOCA is the high temperature corrosion of galvanized steel yielding hydrogen gas. The importance of this source of hydrogen will vary depending on the severity of the accident. In an accident which resulted in core degradation, for example, the major source of hydrogen would probably be the metal-water reaction of the zircaloy cladding, and the corrosion of galvanized steel would then become a relatively minor source of hydrogen. However, in an accident in which core degradation is avoided or limited to minor damage, the corrosion of galvanized steel, and presumably of other materials as well, would then become a major contributor to the buildup of hydrogen within containment. The purpose of this paper is to present the overall effects of temperature, pH, and boric acid concentration on the rate of hydrogen generation over a broad range of each parameter

  11. Analytical and sampling problems in primary coolant circuits of PWR-type reactors

    International Nuclear Information System (INIS)

    Illy, H.

    1980-10-01

    Details of recent analytical methods on the analysis and sampling of a PWR primary coolant are given in the order as follows: sampling and preparation; analysis of the gases dissolved in the water; monitoring of radiating substances; checking of boric acid concentration which controls the reactivity. The bibliography of this work and directions for its use are published in a separate report: KFKI-80-48 (1980). (author)

  12. Radiochemical neutron activation analysis of gold in geochemical samples

    International Nuclear Information System (INIS)

    Zilliacus, R.

    1983-01-01

    A fast method for the radiochemical neutron activation analysis of gold in geochemical samples is described. The method is intended for samples having background concentrations of gold. The method is based on the dissolution of samples with hydrofluoric acid and aqua regia followed by the dissolution of the fluorides with boric acid and hydrochloric acid. Gold is then adsorbed on activated carbon by filtrating the solution through a thin carbon layer. The activity measurements are carried out using a Ge(Li)-detector and a multichannel analyzer. The chemical yields of the separation determined by reirradiation vary between 60 and 90%. The detection limit of the method is 0.2 ng/g gold in rock samples. USGS standard rocks and exploration reference materials are analyzed and the results are presented and compared with literature data. (author)

  13. Crystallo-chemistry of boric anhydride and of anhydrous borates

    International Nuclear Information System (INIS)

    Bernardin, Jacques

    1968-01-01

    After an overview of various aspects related to the atomic structure of boron and of its three-bind and four-bind compounds, this report briefly presents the different forms of boric anhydride (in solid, liquid, glassy and gaseous state), presents and comments the structure of these different forms, and addresses the molten boric anhydride which is used as oxide solvent. The next part addresses the structure of anhydrous borates. It presents some generalities on their structure, and describes examples of known structures: dimers, trimers, polymers with a degree higher than three like calcium metaborate, caesium tri-borate, lithium tetraborate, or potassium pentaborate

  14. Recent bibliography on analytical and sampling problems of a PWR primary coolant

    International Nuclear Information System (INIS)

    Illy, H.

    1980-07-01

    An extensive bibliography on the problems of analysis and sampling of the primary cooling water of PWRs is presented. The aim was to collect the analytical methods for dissolved gases. The sampling and preparation are also taken into account. last 8-10 years is included. The bibliography is arranged into alphabetical order by topics. The most important topics are as follows: boric acid, gas analysis, hydrogen isotopes, iodine, noble gases, radiation monitoring, sampling and preparation, water chemistry. (R.J.)

  15. Recent bibliography on analytical and sampling problems of a PWR primary coolant Suppl. 4

    International Nuclear Information System (INIS)

    Illy, H.

    1986-09-01

    The 4th supplement of a bibliographical series comprising the analytical and sampling problems of the primary coolant of PWR type reactors covers the literature from 1985 up to July 1986 (220 items). References are listed according to the following topics: boric acid; chloride, chlorine; general; hydrogen isotopes; iodine; iodide; noble gases; oxygen; other elements; radiation monitoring; reactor safety; sampling; water chemistry. (V.N.)

  16. Intravaginal boric acid: is it an alternative therapeutic option for vaginal trichomoniasis?

    Science.gov (United States)

    Thorley, Nicola; Ross, Jonathan

    2017-12-09

    Trichomoniasis, caused by Trichomonas vaginalis (TV), is the most common curable sexually transmitted infection worldwide. Current guidance in the UK is to treat TV with a nitroimidazole antibiotic. The high prevalence of TV, high rate of antibiotic resistance and limited tolerability to nitroimidazoles suggest that alternative treatment regimens are needed. Intravaginal boric acid (BA) has been used safely for the treatment of candida vulvovaginitis and bacterial vaginosis, and in vitro studies suggest BA is active against TV. We review the evidence for the efficacy of BA in patients with TV. MEDLINE, EMBASE, CINAHL, AMED, HMIC and BNI and Grey literature databases, The Cochrane Library, Trial Registers, conference abstracts and proceedings were searched. Inclusion criteria were women aged 16 years or over with microbiological confirmation of TV infection and using BA as treatment. There were no restrictions on language, publication date or study design. The in vitro evidence for BA activity against TV was also reviewed. No randomised controlled trials or case series were found. Four case reports demonstrated TV clearance with BA using a variety of dose regimens (dose 600 mg alternate nights to 600 mg two times per day; duration 1-5 months). In vitro studies suggest that BA has activity against TV which is independent of its effect on pH. Further evaluation of BA for the treatment of uncomplicated TV is required, but it may be useful when therapeutic options are limited. If shown to be safe and effective, intravaginal BA might provide a well-tolerated alternative anti-infective treatment which reduces community exposure to systemic antibiotics. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

  17. Improving pitting corrosion resistance of aluminum by anodizing process

    International Nuclear Information System (INIS)

    John, P.; Khan, I.U.

    2013-01-01

    Summary: Anodizing of aluminum was studied in sulphuric/citric/boric acid electrolyte system to improve pitting corrosion resistance. Maximum oxide film thickness was obtained using 5% sulphuric acid, 3% citric acid and 0.5% boric acid electrolyte composition. The corrosion resistance of aluminum sample was determined to find the effectiveness of oxide coating by potentiodynamic polarization test. The surface morphology of aluminum samples was investigated using scanning electron microscope (SEM) before and after corrosion test. It was found that the coated aluminum sample obtained by anodizing in sulphuric/citric/boric acid electrolyte system exhibited better pitting corrosion resistance with no significant difference in surface morphology. (author)

  18. Electrodeposited Fe-Co films prepared from a citric-acid-based plating bath

    OpenAIRE

    Yanai, Takeshi; Uto, H.; Shimokawa, Takaya; Nakano, Masaki; Fukunaga, Hirotoshi; Suzuki, K.

    2013-01-01

    Electrodeposited Fe-Co films are commonly prepared in a boric-acid-based bath. In this research, we applied citric acid instead of boric acid for the plating of Fe-Co films because boron in the waste bath is restricted by environmental-protection regulations in Japan. We evaluated the effect of citric acid on the magnetic and structural properties of the films. The saturation magnetization of the Fe-Co films slightly increased while the Fe content in the Fe-Co films decreased with increasing ...

  19. Direct solid surface fluorescence spectroscopy of standard chemicals and humic acid in ternary system.

    Science.gov (United States)

    Mounier, S; Nicolodelli, G; Redon, R; Milori, D M B P

    2017-04-15

    The front face fluorescence spectroscopy is often used to quantify chemicals in well-known matrices as it is a rapid and powerful technique, with no sample preparation. However it was not used to investigate extracted organic matter like humic substances. This work aims to fully investigate for the first time front face fluorescence spectroscopy response of a ternary system including boric acid, tryptophan and humic substances, and two binaries system containing quinine sulfate or humic substance in boric acid. Pure chemicals, boric acid, tryptophan, quinine sulfate and humic acid were mixed together in solid pellet at different contents from 0 to 100% in mass. The measurement of excitation emission matrix of fluorescence (3D fluorescence) and laser induced fluorescence were then done in the front face mode. Fluorescence matrices were decomposed using the CP/PARAFAC tools after scattering treatments. Results show that for 3D fluorescence there is no specific component for tryptophan and quinine sulfate, and that humic substances lead to a strong extinction effect for mixture containing quinine sulfate. Laser induced fluorescence gives a very good but non-specific related response for both quinine sulfate and tryptophan. No humic substances fluorescence response was found, but extinction effect is observed as for 3D fluorescence. This effect is stronger for quinine sulfate than for tryptophan. These responses were modeled using a simple absorbance versus emission model. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. Evaluating 10B-enriched Boric Acid, Bromide, and Heat as Tracers of Recycled Groundwater Flow near MAR Operations

    Science.gov (United States)

    Becker, T.; Clark, J. F.

    2012-12-01

    County, CA, USA) has been in progress since September 6, 2011, following injection of boric acid enriched in boron-10 (10B) and bromide (Br-) tracers. Tracer concentrations are collected at 9 monitoring wells that have pre-experiment estimated travel times between 0.5 to 180 days. Results indicate that 10B-enriched boric acid is an effective deliberate tracer at MAR sites; however, the ion's movement is slightly retarded relative to bromide by the substrate. 10B/Br- travel time ratios range from 1 to 1.4. In addition to the two deliberate geochemical tracers, heat is being evaluated as a possible intrinsic tracer at MAR sites. At the time of the experiment (late summer), reclaimed water was significantly warmer (~20°F) than the native groundwater as it entered the system. Time series are developed from loggers outfitted at each monitoring well, with measurements recorded hourly accurate to one thousandth of a degree. Results are similar to 10B & Br- travel times and validate the potential of heat as an intrinsic tracer.

  1. Synthesis, characterization and fuel cell performance tests of boric acid and boron phosphate doped, sulphonated and phosphonated poly(vinyl alcohol) based composite membranes

    Science.gov (United States)

    Şahin, Alpay; Ar, İrfan

    2015-08-01

    The aim of this study is to synthesize a composite membrane having high proton conductivity, ion exchange capacity and chemical stability. In order to achieve this aim, poly(vinyl alcohol) (PVA) based composite membranes are synthesized by using classic sol-gel method. Boric acid (H3BO3) and boron phosphate (BPO4) are added to the membrane matrix in different ratios in order to enhance the membrane properties. Characterization tests, i.e; FT-IR analysis, mechanical strength tests, water hold-up capacities, swelling properties, ion exchange capacities, proton conductivities and fuel cell performance tests of synthesized membranes are carried out. As a result of performance experiments highest performance values are obtained for the membrane containing 15% boron phosphate at 0.6 V and 750 mA/cm2. Water hold-up capacity, swelling ratio, ion exchange capacity and proton conductivity of this membrane are found as 56%, 8%, 1.36 meq/g and 0.37 S/cm, respectively. These values are close to the values obtained ones for perfluorosulphonic acid membranes. Therefore this membrane can be regarded as a promising candidate for usage in fuel cells.

  2. Recent bibliography on analytical and sampling problems of a PWR primary coolant Suppl. 3

    International Nuclear Information System (INIS)

    Illy, H.

    1985-03-01

    The present supplement to the bibliography on analytical and sampling problems of PWR primary coolant covers the literature published in 1984 and includes some references overlooked in the previous volumes dealing with the publications of the last 10 years. References are devided into topics characterized by the following headlines: boric acid; chloride; chlorine; carbon dioxide; general; gas analysis; hydrogen isotopes; iodine; iodide; nitrogen; noble gases and radium; ammonia; ammonium; oxygen; other elements; radiation monitoring; reactor safety; sampling; water chemistry. Under a given subject bibliographical information is listed in alphabetical order of the authors. (V.N.)

  3. Investigation of the vaporization of boric acid by transpiration thermogravimetry and knudsen effusion mass spectrometry.

    Science.gov (United States)

    Balasubramanian, R; Lakshmi Narasimhan, T S; Viswanathan, R; Nalini, S

    2008-11-06

    The vaporization of H3BO3(s) was studied by using a commercial thermogravimetric apparatus and a Knudsen effusion mass spectrometer. The thermogravimetric measurements involved use of argon as the carrier gas for vapor transport and derivation of vapor pressures of H3BO3(g) in the temperature range 315-352 K through many flow dependence and temperature dependence runs. The vapor pressures as well as the enthalpy of sublimation obtained in this study represent the first results from measurements at low temperatures that are in accord with the previously reported near-classical transpiration measurements (by Stackelberg et al. 70 years ago) at higher temperatures (382-413 K with steam as the carrier gas). The KEMS measurements performed for the first time on boric acid showed H3BO3(g) as the principal vapor species with no meaningful information discernible on H2O(g) though. The thermodynamic parameters, both p(H3BO3) and Delta sub H degrees m(H3BO3,g), deduced from KEMS results in the temperature range 295-342 K are in excellent agreement with the transpiration results lending further credibility to the latter. All this information points toward congruent vaporization at the H3BO3 composition in the H2O-B2O3 binary system. The vapor pressures obtained from transpiration (this study and that of Stackelberg et al.) as well as from KEMS measurements are combined to recommend the following: log [p(H3BO3)/Pa]=-(5199+/-74)/(T/K)+(15.65+/-0.23), valid for T=295-413 K; and Delta sub H degrees m=98.3+/-9.5 kJ mol (-1) at T=298 K for H3BO3(s)=H3BO3(g).

  4. Reverse osmosis for the recovery of boric acid from the primary coolant at nuclear power plants

    Energy Technology Data Exchange (ETDEWEB)

    Bártová, Šárka, E-mail: sarka.bartova@cvrez.cz [Research Centre Řež Ltd., Husinec-Řež 130, 250 68 Řež (Czech Republic); Kůs, Pavel [Research Centre Řež Ltd., Husinec-Řež 130, 250 68 Řež (Czech Republic); Skala, Martin [Research Centre Řež Ltd., Husinec-Řež 130, 250 68 Řež (Czech Republic); University of Chemical Technology, Prague, Department of Chemical Engineering, Technická 5, Prague 166 28 (Czech Republic); Vonková, Kateřina [Research Centre Řež Ltd., Husinec-Řež 130, 250 68 Řež (Czech Republic)

    2016-04-15

    Highlights: • RO membranes tested for boric acid recovery from primary coolant of nuclear power plants. • Scanning electron microscopy was used for the characterization of the membranes. • Lab scale experiments performed under various operation conditions. • We proposed configuration of and operation conditions for RO unit in nuclear power plant. - Abstract: At nuclear power plants (NPP), evaporators are used for the treatment of primary coolant and other liquid radioactive waste containing H{sub 3}BO{sub 3}. Because the operation of evaporators is expensive, a number of more cost-effective alternatives has been considered, one of which is reverse osmosis. We tested reverse osmosis modules from several manufactures on a batch laboratory apparatus. SEM images of the tested membranes were taken to distinguish the differences between the membranes. Water permeability through membranes was evaluated from the experiments with pure water. The experiments were performed with feed solutions containing various concentrations of H{sub 3}BO{sub 3} in a range commonly occurring in radioactive waste. The pH of the feed solutions ranged from 5.2 to 11.2. Our results confirmed that the pH of the feed solution plays the most important role in membrane separation efficiency of H{sub 3}BO{sub 3}. Certain modifications to the pH of the feed solution were needed to enable the tested membranes to concentrate the H{sub 3}BO{sub 3} in the retentate stream, separate from the pure water in the permeate stream. On this basis, we propose the configuration of and operational conditions for a reverse osmosis unit at NPP.

  5. Boron removal from aqueous solutions by activated carbon impregnated with salicylic acid

    International Nuclear Information System (INIS)

    Celik, Z. Ceylan; Can, B.Z.; Kocakerim, M. Muhtar

    2008-01-01

    In this study, the removal of boric acid from aqueous solution by activated carbon impregnated with salicylic acid was studied in batch system. pH, adsorbent amount, initial boron concentration, temperature, shaking rate and salicylic acid film thickness were chosen as parameters. Boron removal efficiencies increased with increasing adsorbent amount, temperature and pH, decreasing initial boron concentration. As thickness of salicylic acid film on activated carbon becomes thin up to 0.088 nm, the efficiency increased, and then, the efficiency decreased with becoming thinner than 0.088 nm of salicylic acid film. Shaking rate was no effect on removal efficiency. In result, it was determined that the use of salicylic acid as an impregnant for activated carbon led to the increase of the amount of boron adsorbed. A lactone ring, being the most appropriate conformation, forms between boric acid and -COOH and -OH groups of salicylic acid

  6. Boron removal from aqueous solutions by activated carbon impregnated with salicylic acid

    Energy Technology Data Exchange (ETDEWEB)

    Celik, Z. Ceylan [Department of Environmental Engineering, Atatuerk University, Faculty of Engineering, Erzurum (Turkey)], E-mail: zcelik@atauni.edu.tr; Can, B.Z. [Department of Environmental Engineering, Atatuerk University, Faculty of Engineering, Erzurum (Turkey); Kocakerim, M. Muhtar [Department of Chemical Engineering, Atatuerk University, Faculty of Engineering, 25240 Erzurum (Turkey)

    2008-03-21

    In this study, the removal of boric acid from aqueous solution by activated carbon impregnated with salicylic acid was studied in batch system. pH, adsorbent amount, initial boron concentration, temperature, shaking rate and salicylic acid film thickness were chosen as parameters. Boron removal efficiencies increased with increasing adsorbent amount, temperature and pH, decreasing initial boron concentration. As thickness of salicylic acid film on activated carbon becomes thin up to 0.088 nm, the efficiency increased, and then, the efficiency decreased with becoming thinner than 0.088 nm of salicylic acid film. Shaking rate was no effect on removal efficiency. In result, it was determined that the use of salicylic acid as an impregnant for activated carbon led to the increase of the amount of boron adsorbed. A lactone ring, being the most appropriate conformation, forms between boric acid and -COOH and -OH groups of salicylic acid.

  7. THE KINETICS OF SAPONIFICATION OF IODOACETIC ACID BY SODIUM HYDROXIDE AND BY CERTAIN ALKALINE BUFFER SOLUTIONS.

    Science.gov (United States)

    Brdicka, R

    1936-07-20

    1. The rate of the saponification of iodoacetic acid in sodium hydroxide and alkaline buffer solutions yielding glycollic acid was measured by means of Heyrovský's polarographic method. 2. From the bimolecular velocity constants, increasing with the ionic strength of the solution, the Brönsted factor, F, which characterizes the primary salt effect, was calculated. 3. In the borate buffer solutions the monomolecular constants of the saponification were determined which, at values above the pH of neutralization of boric acid, show a proportionality to the concentration of hydroxyl anions. Below the pH of neutralization of boric acid, they are proportional to the concentration of borate anions.

  8. The preservation of urine samples for determination of renal stone risk factors

    Science.gov (United States)

    Nicar, M. J.; Hsu, M. C.; Johnson, T.; Pak, C. Y.

    1987-01-01

    A preservation technique for urine specimens before determination of stone risk factors was evaluated. The purpose of these experiments was to prove the effectiveness of the preservatives used to prevent changes in the concentrations of those constituents measured. Measured concentrations in fresh specimens were compared with those in the same specimens after storage with the preservatives. Refrigeration at 4 degrees C up to five days was appropriate in a laboratory setting, as no significant changes in urinary concentrations occurred. Refrigeration, however, did not offer a convenient method for shipping. Chemical preservation was found to be an effective alternative to refrigeration. Thymol prevented changes in concentration of pH, citrate, uric acid, sulfate, sodium, potassium, and cyclic AMP, while a mixture of hydrochloric (HCl) acid and boric acid prevented changes in calcium, magnesium, phosphorus, oxalate, ammonium, and creatinine. Thus, the addition of thymol or HCl/boric acid to urine specimens will prevent significant changes in the concentrations of stone risk factors.

  9. Theoretical isotopic fractionation between structural boron in carbonates and aqueous boric acid and borate ion

    Science.gov (United States)

    Balan, Etienne; Noireaux, Johanna; Mavromatis, Vasileios; Saldi, Giuseppe D.; Montouillout, Valérie; Blanchard, Marc; Pietrucci, Fabio; Gervais, Christel; Rustad, James R.; Schott, Jacques; Gaillardet, Jérôme

    2018-02-01

    The 11B/10B ratio in calcite and aragonite is an important proxy of oceanic water pH. However, the physico-chemical mechanisms underpinning this approach are still poorly known. In the present study, we theoretically determine the equilibrium isotopic fractionation properties of structural boron species in calcium carbonates, BO33-, BO2(OH)2- and B(OH)4- anions substituted for carbonate groups, as well as those of B(OH)4- and B(OH)3 species in vacuum. Significant variability of equilibrium isotopic fractionation properties is observed among these structural species which is related to their contrasted coordination state, Bsbnd O bond lengths and atomic-scale environment. The isotopic composition of structural boron does not only depend on its coordination number but also on its medium range environment, i.e. farther than its first coordination shell. The isotopic fractionation between aqueous species and their counterparts in vacuum are assessed using previous investigations based on similar quantum-mechanical modeling approaches. At 300 K, the equilibrium isotope composition of structural trigonal species is 7-15‰ lighter than that of aqueous boric acid molecules, whereas substituted tetrahedral borate ions are heavier than their aqueous counterparts by 10-13‰. Although significant uncertainties are known to affect the theoretical prediction of fractionation factors between solids and solutions, the usually assumed lack of isotopic fractionation during borate incorporation in carbonates is challenged by these theoretical results. The present theoretical equilibrium fractionation factors between structural boron and aqueous species differ from those inferred from experiments which may indicate that isotopic equilibrium, unlike chemical equilibrium, was not reached in most experiments. Further research into the isotopic fractionation processes at the interface between calcium carbonates and aqueous solution as well as long duration experiments aimed at

  10. Determination of organic acids evolution during apple cider fermentation using an improved HPLC analysis method

    NARCIS (Netherlands)

    Zhang, H.; Zhou, F.; Ji, B.; Nout, M.J.R.; Fang, Q.; Zhang, Z.

    2008-01-01

    An efficient method for analyzing ten organic acids in food, namely citric, pyruvic, malic, lactic, succinic, formic, acetic, adipic, propionic and butyric acids, using HPLC was developed. Boric acid was added into the mobile phase to separate lactic and succinic acids, and a post-column buffer

  11. Synthesis of trialkyloboron from boric oxide and organoaluminium compounds

    International Nuclear Information System (INIS)

    Synoradzki, L.; Boleslawski, M.; Pasynkiewicz, S.; Zawada, T.

    1981-01-01

    The reaction of organoaluminium compounds with boric oxide has been studied. The facility of forming trialkyloboron decreases corresponding to the sequence: RAlCl 2 >R 3 Al 2 Cl 3 >R 2 AlCl>R 3 Al. The best yields have been obtained at the temperature of the boiling point of the reaction mixture and at a vigorous mixing. The new method of simultaneous obtaining of trialkyloboron and alkylaluminium chloride having an industrial significance has been proposed. (author)

  12. Preparation of rock samples for measurement of the thermal neutron macroscopic absorption cross-section

    International Nuclear Information System (INIS)

    Czubek, J.A.; Burda, J.; Drozdowicz, K.; Igielski, A.; Kowalik, W.; Krynicka-Drozdowicz, E.; Woznicka, U.

    1986-03-01

    Preparation of rock samples for the measurement of the thermal neutron macroscopic absorption cross-section in small cylindrical two-region systems by a pulsed technique is presented. Requirements which should be fulfilled during the preparation of the samples due to physical assumptions of the method are given. A cylindrical vessel is filled with crushed rock and saturated with a medium strongly absorbing thermal neutrons. Water solutions of boric acid of well-known macroscopic absorption cross-section are used. Mass contributions of the components in the sample are specified. This is necessary for the calculation of the thermal neutron macroscopic absorption cross-section of the rock matrix. The conditions necessary for assuring the required accuracy of the measurement are given and the detailed procedure of preparation of the rock sample is described. (author)

  13. Enraizamento de estacas do porta-enxerto de videira 'vr 043-43' submetidas a estratificação, ácido indolbutírico e ácido bórico Rooting cuttings of rootstocks of grape vine 'vr 043-43' submitted to the stratification, indolebutyric acid and boric acid

    Directory of Open Access Journals (Sweden)

    Ariane Busch Salibe

    2010-01-01

    Full Text Available O presente trabalho teve como objetivo estudar o enraizamento de estacas de porta-enxerto 'VR 043-43' (V. vinifera x V. rotundifolia, testando diferentes concentrações de ácido indolbutírico (0, 1.000, 2.000 e 3.000 mg L-1, ácido bórico (0 e 150 µg L-1 e a técnica de estratificação a 4 ºC por 48 horas em câmara refrigerada. Utilizou-se o delineamento experimental em blocos inteiramente casualizados, em esquema fatorial 4 x 2 x 2, com cinco repetições e cada parcela representada por oito estacas. Após 120 dias do plantio das estacas, os seguintes dados biométricos foram mensurados: porcentagem de estacas enraizadas, comprimento médio radicial, massa da parte aérea, massa do sistema radicial e número de raízes. Verificou-se que a estratificação das estacas e a utilização de ácido bórico não afetaram o enraizamento do porta-enxerto 'VR 043-43'. No que se refere ao tratamento com ácido indolbutírico, a concentração de 3.000 mg L-1 favoreceu sensivelmente o desenvolvimento do sistema radicial das estacas do porta-enxerto.The present work had as objective to study the rooting of rootstocks 'VR 043-43' (V. vinifera x V. rotundifolia, testing different concentrations of indolebutyric acid (0, 1.000, 2.000 and 3.000 mg L-1, boric acid (0 and 150 μg L-1 and the technique of the stratification at 4 °C for 48 hours in cooled chamber. We used a randomized complete block design, in factorial scheme 4 x 2 x 2, with five repetitions and each parcel represented for eight cuttings. After 120 days of planting the cuttings, the following biometric data were measured: percentage of rooting cuttings, average length root, mass of the aerial part, mass of the radicial system and number of roots. It was verified that the stratification of the cuttings and the use of boric acid did not affect the rooting of the rootstocks 'VR 043-43'. With regard the treatment with indolebutyric acid, the concentration of 3.000 mg L-1 significantly

  14. Effect of the calcium, boron and sulphur in pre harvest applications over the severity of anthracnose(Colletotrichum gloeosporioides Penz.) and the fruit's quality of two papaya's varieties in Perez Zeledon

    International Nuclear Information System (INIS)

    Montealegre Perez, Eduardo Antonio

    2005-01-01

    This research established the effect of the calcium, boron and sulphur in pre harvest applications over the severity of anthracnosis (Colletotrichum gloeosporioides Penz.) and the fruit's quality of two papaya's varieties, one creole and a hibrido in Perez Zeledon. The treatments were the folloguings: oxide of calcium plus dolomite, oxide of calcium plus boric acid plus dolomite, boric acid plus sulphate of potassium and dolomite, boric acid less dolomite and witness. The utilized sources were nitrate of calcium, boric acid and sulphate of potassium. The evaluations were realized both in the rainy season like in the dry season. There were evaluated: severity of anthracnosis, weight of the fruits, total soluble solids, shell's hardness, and stability of the flesh. The experimental design utilized was a complete block at random. There were got that the applications of oxide of calcium and boric acid less dolomite decreased the severity of the disease in the papaya's fruits, while that the boric acid plus sulphate tend to increase the disease. The treatment of boric acid plus sulphate decreased the weight of the fruits both in the rainy and dry season. Besides this treatment decreased the hardness of the shell, while that the treatments with boron increased that. Also the treatments with boric acid plus dolomite and boric acid less dolomite, increased the levels of total soluble solids in the papaya's fruits in the two varieties. Finally; the treatments: oxide of calcium plus boric acid and boric acid plus sulphate decreased the stability of the flesh in both varieties and both evaluated seasons, while the treatment with oxide of calcium increased the stability of the flesh in the hibrido during the dry season. (Author) [es

  15. 3.6. The kinetics of sulfuric acid decomposition of calcined concentrate of borosilicate ore

    International Nuclear Information System (INIS)

    Mirsaidov, U.M.; Kurbonov, A.S.; Mamatov, E.D.

    2015-01-01

    Present article is devoted to kinetics of sulfuric acid decomposition of calcined concentrate of borosilicate ore. The experimental data of kinetics of extraction of boron oxide from danburite at sulfuric acid decomposition were obtained at 20-90 deg C temperature range and process duration 15-90 minutes. The flowsheet of obtaining of boric acid from borosilicate ores of Ak-Arkhar Deposit by sulfuric acid method was proposed.

  16. An X-ray fluorescence method for the determination of Ba, Sr, Mo and Bi in thorium oxide

    International Nuclear Information System (INIS)

    Dixit, R.M.; Deshpande, S.S.

    1988-01-01

    A simple and rapid X-ray fluorescence method for the determination of Ba, Sr, Mo and Bi in thoria is described. Thorium oxide samples are dry-mixed thoroughly with pure boric acid in the ratio of 9:1. One gram of mixture is pressed as a double layer over a primary boric acid pellet. The precision and accuracy of the method have been determined. The power limits of detection are found to be around 20 ppm for most analytes. (author). 5 tables

  17. Viabilidade in vitro de grãos de pólen de bananeira sob diferentes concentrações de ácido bórico e sacarose In vitro viability of banana pollen grain under different concentrations of boric acid and sucrose

    Directory of Open Access Journals (Sweden)

    Ronaldo Viana dos Reis

    2011-06-01

    Full Text Available Neste trabalho, objetivou-se avaliar a germinação do grão de pólen e o comprimento do tubo polínico das bananeiras diplóides M53, 8987-01 e 9197-03, Calcutá, Lidi e 86B79-12. O delineamento utilizado foi inteiramente casualizado com cinco doses de sacarose (0, 5, 10, 15, 20% e seis concentrações de ácido bórico (0, 100, 200, 300, 400 e 500 Mg L-1 com quatro repetições. Foram utilizados grãos de pólen retirados da inflorescência masculina dos diplóides Musa acuminata (AA. O pólen foi distribuído em placas de Petri, contendo o seguinte meio de cultura: 1,27 mM de Ca(NO32.2H2O, 0,87 mM de MgSO4.7H2O, 0,99 mM de KNO3, 0,7% de ágar com pH ajustado para 7,0, variando as concentrações de sacarose e de ácido bórico. As avaliações foram realizadas 24 horas após a distribuição do pólen no meio de cultura. O meio de cultura padrão para germinação de grãos de pólen suplementado com 15% de sacarose proporcionou uma maior percentagem de germinação para os diplóides de bananeira avaliados. A concentração de ácido bórico adicionado ao meio de cultura para a germinação de grãos de pólen de bananeira diplóide é dependente do genótipo.The objective of this work was to evaluate the germination of pollen grain and pollen tube length of banana diploids (M53, 8987-01 e 9197-03, Calcutta, Lidi and 86B79-12. Five concentrations of sucrose (0, 5, 10, 15 and 20% and six concentrations of boric acid (0, 100, 200, 300, 400 and 500 mg L-1 were used, in a completely randomized experimental design, with four replicates. The pollen was distributed in Petri dishes containing the following culture medium: 1.27 mM Ca(NO32.2H2O, 0.87 mM MgSO4.7H2O, 0.99 mM KNO3, and 0.7% agar; pH adjusted to 7.0, varying the sucrose and boric acid concentrations. The evaluations were performed 24 hours after the distribution of the pollen in the culture medium. The standard culture medium for germination of pollen grains with 15% sucrose provided the

  18. Effect of Relative Humidity on the Tribological Properties of Self-Lubricating H3BO3 Films Formed on the Surface of Steel Suitable for Biomedical Applications

    Directory of Open Access Journals (Sweden)

    E. Hernández-Sanchez

    2015-01-01

    Full Text Available The effect of environmental humidity on the self-lubricating properties of a thin film of boric acid (H3BO3 was evaluated. H3BO4 films were successfully formed on the surface of AISI 316L steel. The study was conducted on AISI 316L steel because of its use in biomedical applications. First, the samples were exposed to boriding to generate a continuous surface layer of iron borides. The samples were then exposed to a short annealing process (SAP at 1023 K for 5 min and cooled to room temperature while controlling the relative humidity (RH. Five different RH conditions were tested. The purpose of SAP was to promote the formation of a surface film of boric acid from the boron atoms present in the iron boride layers. The presence of the boric acid at the surface of the borided layer was confirmed by Raman spectroscopy and X-ray diffraction (XRD. The self-lubricating capability of the films was demonstrated using the pin-on-disk technique. The influence of RH was reflected by the friction coefficient (FC, as the samples cooled with 20% of RH exhibited FC values of 0.16, whereas the samples cooled at 60% RH showed FC values of 0.02.

  19. Introduction - Acid decomposition of borosilicate ores

    International Nuclear Information System (INIS)

    Mirsaidov, U.M.; Kurbonov, A.S.; Mamatov, E.D.

    2015-01-01

    The complex processing of mineral raw materials is an effective way for the extraction of valuable components. One of these raw materials are borosilicate ores from which the boric acid, aluminium and iron salts and building materials can be obtained. In the Institute of Chemistry of the Academy of Sciences of the Republic of Tajikistan the flowsheets of the processing of borosilicate raw materials by acid and chloric methods were elaborated. The acid methods of decomposition of borosilicate ores of Ak-Arkhar Deposit were considered in present monograph. The carried out researches on elaboration of physicochemical aspects and technological acid methods allowed to define the optimal ways of extraction of valuable products from borosilicate raw materials of Tajikistan.

  20. X-ray fluorescence analysis of lutetium oxide/oxalate for rare earth impurities

    International Nuclear Information System (INIS)

    Chandola, L.C.; Khanna, P.P.

    1985-01-01

    An X-ray fluorescence spectrometric method for the analysis of lutetium oxide is described. The sample in the oxalate form is mixed with boric acid binding material and pressed into a pellet over supporting pellet of boric acid. A Philips PW 1220 wavelength dispersive semiautomatic X-ray fluorescence spectrometer is used for the analysis. The minimum determination limit is 0.002 percent for Y, Er and Yb and 0.005 percent for Tm. Calculations for theoretical minimum detection limits and percent standard deviations at each concentration of the standard are carried out. (author)

  1. The Origin of Amino Acids in Lunar Regolith Samples

    Science.gov (United States)

    Cook, Jamie E.; Callahan, Michael P.; Dworkin, Jason P.; Glavin, Daniel P.; McLain, Hannah L.; Noble, Sarah K.; Gibson, Everett K., Jr.

    2016-01-01

    We analyzed the amino acid content of seven lunar regolith samples returned by the Apollo 16 and Apollo 17 missions and stored under NASA curation since collection using ultrahigh-performance liquid chromatography with fluorescence detection and time-of-flight mass spectrometry. Consistent with results from initial analyses shortly after collection in the 1970s, we observed amino acids at low concentrations in all of the curated samples, ranging from 0.2 parts-per-billion (ppb) to 42.7 ppb in hot-water extracts and 14.5 ppb to 651.1 ppb in 6M HCl acid-vapor-hydrolyzed, hot-water extracts. Amino acids identified in the Apollo soil extracts include glycine, D- and L-alanine, D- and L-aspartic acid, D- and L-glutamic acid, D- and L-serine, L-threonine, and L-valine, all of which had previously been detected in lunar samples, as well as several compounds not previously identified in lunar regoliths: -aminoisobutyric acid (AIB), D-and L-amino-n-butyric acid (-ABA), DL-amino-n-butyric acid, -amino-n-butyric acid, -alanine, and -amino-n-caproic acid. We observed an excess of the L enantiomer in most of the detected proteinogenic amino acids, but racemic alanine and racemic -ABA were present in some samples.

  2. Boron isotope separation by ion exchange chromatography using weakly basic anion exchange resin

    International Nuclear Information System (INIS)

    Itoh, S.; Aida, M.; Okamoto, M.; Nomura, M.; Fujii, Y.

    1985-01-01

    Influences of operating temperatures and concentrations of feed boric acid solutions were examined on the above titled process over the ranges of 25 - 70 0 C and 0.1 - 1.6 mol/dm 3 (M), respectively. The ideal displacement chromatography with a very sharp-cut boundary of the boric acid adsorption band was realized at higher temperatures and lower boric acid concentrations within the experimental conditions. The isotope separation coefficient epsilon was found to decrease with increases in either temperature or the boric acid concentration. The observed values of epsilon at 25 0 C were 0.013, 0.012 and 0.011 corresponding to feed boric acid concentrations of 0.1 M, 0.4 M and 0.8 M, respectively. The epsilon's at 70 0 C were 0.0097 (0.1 M), 0.0086 (0.4 M), 0.0083 (0.8 M) and 0.0073 (1.6 M). A temperature of 40 0 C and 0.4 M of boric acid concentration was considered the optimum operating condition for the production of enriched 10 B. (author)

  3. The nitric acid decomposition of calcined danburite concentrate of Ak-Arkhar Deposit

    International Nuclear Information System (INIS)

    Kurbonov, A.S.; Mamatov, E.D.; Suleymani, M.; Borudzherdi, A.; Mirsaidov, U.M.

    2011-01-01

    Present article is devoted to nitric acid decomposition of calcined danburite concentrate of Ak-Arkhar Deposit of Tajikistan. The obtaining of boric acid from pre backed danburite concentrate by decomposition of nitric acid was studied. The chemical composition of danburite concentrate was determined. The laboratory study of danburite leaching by nitric acid was conducted. The influence of temperature, process duration, nitric acid concentration on nitric acid decomposition of calcined danburite concentrate of Ak-Arkhar Deposit was studied as well. The optimal conditions of nitric acid decomposition of calcined danburite concentrate of Ak-Arkhar Deposit, including temperature, process duration, nitric acid concentration and particle size were proposed.

  4. Analysis of Rock-Geological Material From Places in Tanzania by ...

    African Journals Online (AJOL)

    Dispersive X-ray Fluorescence (WDXRF) Analysis has been used with objective of ... The samples identified and reported in this paper include: Iron ore, ... The samples were prepared as pellets after mixing with boric acid or fused as discs for

  5. Distribution and Origin of Amino Acids in Lunar Regolith Samples

    Science.gov (United States)

    Elsila, J. E.; Callahan, M. P.; Glavin, D. P.; Dworkin, J. P.; McLain, H. L.; Noble, S. K.; Gibson, E. K., Jr.

    2015-01-01

    The existence of organic compounds on the lunar surface has been a question of interest from the Apollo era to the present. Investigations of amino acids immediately after collection of lunar samples yielded inconclusive identifications, in part due to analytical limitations including insensitivity to certain compounds, an inability to separate enantiomers, and lack of compound-specific isotopic measurements. It was not possible to determine if the detected amino acids were indigenous to the lunar samples or the result of terrestrial contamination. Recently, we presented initial data from the analysis of amino acid abundances in 12 lunar regolith samples and discussed those results in the context of four potential amino acid sources [5]. Here, we expand on our previous work, focusing on amino acid abundances and distributions in seven regolith samples and presenting the first compound-specific carbon isotopic ratios measured for amino acids in a lunar sample.

  6. The development of radioactive waste treatment technology (III)

    International Nuclear Information System (INIS)

    Kim, Joon Hyung; Jung, Ki Jung; Lee, Kune Woo; Park, Hun Hwee

    1991-03-01

    Most PWR stations have experienced leakages of boric acid and oil into liquid radwaste systems. Typically, these wastes have been concentrated by an evaporator system. Based on operating plant experiences, boric acid and oil are the majority of the solid loading for disposal and tend to decrease the efficiency significantly. The objective of these studies is to develop pretreatment techniques for the recovery of boric acid and for the removal of oil from such wastes for improving the evaporator performance. To these objectives, lab. scale reverse osmosis (RO) membrane and filtration/coalescence processes are introduced, which can separate boric acid and oil into waste streams. (Author)

  7. Radiocarbon variability of fatty acids in semi-urban aerosol samples

    International Nuclear Information System (INIS)

    Matsumoto, Kohei; Uchida, Masao; Kawamura, Kimitaka; Shibata, Yasuyuki; Morita, Masatoshi

    2004-01-01

    We analyzed radiocarbon and the stable carbon isotope ratio for individual monocarboxylic (fatty) acids in an aerosol sample (QFF 2138) and compared the results with data of the aerosol sample taken in another year. The fatty acid concentration distribution of aerosol sample QFF 2138 showed a bimodal pattern with maxima at C 16 and C 26 . Stable carbon isotope ratios of the fatty acids ranged from -30.8 per mille to -23.0 per mille which indicates the animal and/or marine algae origins for C 16 -C 19 fatty acids and mainly terrestrial C 3 plant origins for C >20 fatty acids. Δ 14 C values for fatty acids ranged from -89.7 per mille to +83.5 per mille. Compared with QFF1969, we found that the Δ 14 C values of fatty acids exhibited a wide diversity and Δ 14 C values for each fatty acid in QFF 2138 were largely different from those of QFF 1969

  8. X-ray fluorescence analysis of thulium oxide/oxalate for rare earth impurities

    International Nuclear Information System (INIS)

    Chandola, L.C.; Khanna, P.P.

    1986-01-01

    An X-ray fluorescence spectrometric method for the analysis of thulium oxide is described. For the analysis, the sample in oxalate form is mixed with boric acid binding material and pressed into a pellet over a supporting pellet of boric acid. A wavelength dispersive Philips PW 1220 X-ray fluorescence spectrometer is used for the experiments; the minimum determination limits are 0.002per cent for Ho, Lu and Y, 0.005per cent for Dy and Er and 0.01per cent for Yb. Calculations for theoretical minimum detection limits and percent standard deviation at each concentration of the standard are carried out. (author)

  9. Determination of very small contents of boron by pH difference measurement

    International Nuclear Information System (INIS)

    Boehm, H.; Kirmse, E.M.; Schilbach, U.

    1983-01-01

    For the determination of boron as a trace element for food of plants in a very complicated salt matrix an analytical proceeding was developed, which allows to determine the content of boron without separation. The principle of analysis is based on the esterification of boric acid with a multivalent alcohol, which leeds to a monovalent strong complex acid. The change of the pH value of the analysing solution is measured. From the initial pH number, the end pH number, the volume of the analysing solution and the ionic product of water corresponding with the operating temperature the quantity of boric acid of boron that is equivalent the produced quantity of H + -ions is calculated by means of a linear program. The standard deviation of analytical proceeding amounts to 13.9 ng B. For the determination of the contents of boron of an unknown sample, five to ten separate measurements are carried out. For solutions, which are about 1x10 -6 M of boric acid, there are necessary 10 ml of sample for each separate measurement. The confidence interval of analytical results is found to be between +- 0.5 and +- 15.5% (P=0.99). For the determination of the content of boron in plant materials about 50-100 mg of dry weight are necessary. (Author)

  10. Method of processing radioactive liquid wastes

    Energy Technology Data Exchange (ETDEWEB)

    Sugimoto, Y; Kikuchi, M; Funabashi, K; Yusa, H; Horiuchi, S

    1978-12-21

    Purpose: To decrease the volume of radioactive liquid wastes essentially consisting of sodium hydroxide and boric acid. Method: The concentration ratio of sodium hydroxide to boric acid by weight in radioactive liquid wastes essentially consisting of sodium hydroxide and boric acid is adjusted in the range of 0.28 - 0.4 by means of a pH detector and a sodium concentration detector. Thereafter, the radioactive liquid wastes are dried into powder and then discharged.

  11. Immobilized laccase mediated dye decolorization and transformation pathway of azo dye acid red 27

    OpenAIRE

    Chhabra, Meenu; Mishra, Saroj; Sreekrishnan, Trichur Ramaswamy

    2015-01-01

    Background Laccases have good potential as bioremediating agents and can be used continuously in the immobilized form like many other enzymes. Methods In the present study, laccase from Cyathus bulleri was immobilized by entrapment in Poly Vinyl Alcohol (PVA) beads cross-linked with either nitrate or boric acid. Immobilized laccase was used for dye decolorization in both batch and continuous mode employing a packed bed column. The products of degradation of dye Acid Red 27 were identified by ...

  12. 4.2. The kinetics of nitric acid decomposition of calcined borosilicate raw material of Ak-Arkhar Deposit

    International Nuclear Information System (INIS)

    Mirsaidov, U.M.; Kurbonov, A.S.; Mamatov, E.D.

    2015-01-01

    Present article is devoted to kinetics of nitric acid decomposition of calcined borosilicate raw material of Ak-Arkhar Deposit. The dependence of nitric acid decomposition of calcined boric raw material for extraction of boron oxide on temperature (20-100 deg C) and process duration (15-60 minutes) was defined. It was defined that at temperature increasing the extraction rate of boron oxide increases from 20.8 to 78.6%.

  13. Enraizamento de estacas de Ginkgo biloba tratadas com ácido indolbutírico e ácido bórico Rooting of Ginkgo biloba cuttings treated with indolbutyric and boric acids

    Directory of Open Access Journals (Sweden)

    Janice Valmorbida

    2008-04-01

    Full Text Available Objetivou-se neste trabalho estudar o efeito do ácido indolbutírico (AIB e do ácido bórico (B no enraizamento de estacas de Ginkgo biloba. Em estacas com duas folhas, medindo 15 cm de comprimento foram provocadas duas lesões na base de aproximadamente 2 cm, expondo o câmbio e procedeu-se à imersão por 10 segundos no tratamento correspondente, AIB (0, 1000, 2000 e 3000 mg L-1 na ausência ou presença de B (0 e 150 mg L-1. Em seguida foram colocadas para enraizar em bandejas de polipropileno contendo areia lavada. O delineamento foi em blocos casualizados num fatorial 4X2, com seis repetições. Foram avaliadas porcentagem de estacas enraizadas, estacas não enraizadas e mortas, diâmetro e comprimento das raízes, aos 70 dias do tratamento. Os dados foram submetidos à análise de variância sendo previamente testados para normalidade pelo Teste de Shapiro-Wilk. As médias foram comparadas pelo Teste de Tukey. Os tratamentos com 2000 mg L-1 de AIB foram superiores à ausência de AIB (80,55% vs. 55,56%, respectivamente, não diferindo dos demais tratamentos. A utilização de B não afetou a taxa de enraizamento, de estacas não enraizadas e mortas, não havendo interação entre a concentração de AIB e a utilização ou não de B. O diâmetro e o comprimento das raízes não foram afetados pela utilização de AIB e B.The aim of the work was to study the effect of indolbutyric (IBA and boric (B acids to root Ginkgo biloba cuttings. At the base of cuttings, with two leaves and 15 cm of length, were made two lesions with 2 cm to expose the cambium. Cuttings were treated for a period of 10 seconds with four concentrations of IBA (0, 1000, 2000 and 3000 mg L-1 combined with two concentration of B (0 and 150 mg L-1. After that, cuttings were taken in polypropylene trays filled with washed sand. The experimental design was of randomized blocks in the factorial arrangement (4x2, with six replications. After 70 days, evaluations were done

  14. Selenium speciation in acidic environmental samples: application to acid rain-soil interaction at Mount Etna volcano.

    Science.gov (United States)

    Floor, Geerke H; Iglesías, Mònica; Román-Ross, Gabriela; Corvini, Philippe F X; Lenz, Markus

    2011-09-01

    Speciation plays a crucial role in elemental mobility. However, trace level selenium (Se) speciation analyses in aqueous samples from acidic environments are hampered due to adsorption of the analytes (i.e. selenate, selenite) on precipitates. Such solid phases can form during pH adaptation up till now necessary for chromatographic separation. Thermodynamic calculations in this study predicted that a pHpH eluent that matches the natural sample pH of acid rain-soil interaction samples from Etna volcano was developed. With a mobile phase containing 20mM ammonium citrate at pH 3, selenate and selenite could be separated in different acidic media (spiked water, rain, soil leachates) in rain-soil interaction using synthetic rain based on H(2)SO(4) and soil samples collected at the flanks of Etna volcano demonstrated the dominance of selenate over selenite in leachates from samples collected close to the volcanic craters. This suggests that competitive behavior with sulfate present in acid rain might be a key factor in Se mobilization. The developed speciation method can significantly contribute to understand Se cycling in acidic, Al/Fe rich environments. Copyright © 2011 Elsevier Ltd. All rights reserved.

  15. Determination of Ti, Cr, Cu and Ta in niobium oxide by X-ray fluorescence method

    International Nuclear Information System (INIS)

    Dixit, R.M.; Deshpande, S.S.

    1986-01-01

    An x-ray fluorescence method for the determination of Ti, Cr, Cu and Ta in niobium oxide has been developed. Samples/standards in powder form are mixed with boric acid in the proportion of 1:1 (400 mg. each). Double layer pellets are prepared by pressing this mixture over a primary boric acid pellet. Philips PW-1220, a semiautomatic x-ray spectrometer with tungsten target x-ray tube for excitation and LiF (200) crystal for dispersion have been used. The determination range is from 0.005 to 0.1per cent for Ti and Cr, 0.01 to 0.1per cent for Cu and 0.05 to 1per cent for Ta. (author)

  16. Acid-permanganate oxidation of potassium tetraphenylboron

    International Nuclear Information System (INIS)

    Smith, J.R.

    1993-02-01

    Scoping experiments have been performed which show that potassium tetraphenylboron (KTPB) is rapidly oxidized by permanganate in acidic solutions at room temperature. The main Products are CO 2 , highly oxidized organic compounds related to tartaric and tartronic acids, boric acid, and potassium phosphate (when phosphoric acid is used as the source of acid). One liter of 0.6M NaMnO 4 /2.5M H 3 PO 4 solution will destroy up to 8 grams of KTPB. The residual benzene concentration has been measured to be less than the RCRA limit of 0.5 ppm. Approximately 30% of the organic material is released as CO 2 (trace CO) and 0.16% as benzene vapor. The reaction is well behaved, no foaming or spattering. Tests were performed from .15M to near 1M permanganate. The phosphoric acid concentration was maintained at a concentration at least three times that of the permanganate since an excess of acid was desired and this is the ratio that these two reagents are consumed in the oxidation

  17. X-ray fluorescence analysis of ytterbium oxide/oxalate for rare earth impurities

    International Nuclear Information System (INIS)

    Chandola, L.C.; Khanna, P.P.; Thomas, A.

    1982-01-01

    An XRF method for the determination of Ho, Er, Tm, Lu and Y oxides in Yb 2 O 3 is described. 450 mg sample in the oxalate form is mixed with 150 mg boric acid binding material and pressed into 1.25 inch diameter pellet over a supporting pellet of boric acid. The sample is irradiated by X-rays from a tungsten tube and the fluorescent X-rays are dispersed by a LiF(200) crystal in a Philips PW 1220 semiautomatic X-ray fluorescence spectrometer. The intensities of characteristic X-rays of the impurity elements are measured by a flow proportional counter or a scintillation counter. The lowest determination limit is 0.005% for Ho, Er, Tm and Y and 0.01% for Lu. Calculations for theoretical detection limit, standard deviation and uncertainty are done and presented. (author)

  18. Deboration in nuclear stations of the PWR type

    International Nuclear Information System (INIS)

    1978-01-01

    Reactivity control in nuclear power stations of the PWR type is realised with boric acid. A method to concentrate boric acid without an evaporator has been studied. A flow-sheet with reverse osmosis is proposed. (author)

  19. Integrated sample-to-detection chip for nucleic acid test assays.

    Science.gov (United States)

    Prakash, R; Pabbaraju, K; Wong, S; Tellier, R; Kaler, K V I S

    2016-06-01

    Nucleic acid based diagnostic techniques are routinely used for the detection of infectious agents. Most of these assays rely on nucleic acid extraction platforms for the extraction and purification of nucleic acids and a separate real-time PCR platform for quantitative nucleic acid amplification tests (NATs). Several microfluidic lab on chip (LOC) technologies have been developed, where mechanical and chemical methods are used for the extraction and purification of nucleic acids. Microfluidic technologies have also been effectively utilized for chip based real-time PCR assays. However, there are few examples of microfluidic systems which have successfully integrated these two key processes. In this study, we have implemented an electro-actuation based LOC micro-device that leverages multi-frequency actuation of samples and reagents droplets for chip based nucleic acid extraction and real-time, reverse transcription (RT) PCR (qRT-PCR) amplification from clinical samples. Our prototype micro-device combines chemical lysis with electric field assisted isolation of nucleic acid in a four channel parallel processing scheme. Furthermore, a four channel parallel qRT-PCR amplification and detection assay is integrated to deliver the sample-to-detection NAT chip. The NAT chip combines dielectrophoresis and electrostatic/electrowetting actuation methods with resistive micro-heaters and temperature sensors to perform chip based integrated NATs. The two chip modules have been validated using different panels of clinical samples and their performance compared with standard platforms. This study has established that our integrated NAT chip system has a sensitivity and specificity comparable to that of the standard platforms while providing up to 10 fold reduction in sample/reagent volumes.

  20. Ecofriendly Fire Retardant and Rot Resistance Finishing of Jute Fabric Using Tin and Boron Based Compound

    Science.gov (United States)

    Samanta, Ashis Kumar; Bagchi, Arindam

    2017-06-01

    Treatment with sodium stannate followed by treatment with boric acid imparts jute fabric wash fast fire resistance property as indicated by its Limiting Oxygen Index (LOI) value and 45° inclined flammability test results. The treatment was carried out by impregnation of sodium stannate followed by impregnation with an aqueous solution of boric acid and drying. Application of sodium stannate (20%) and boric acid (20%) treatment on jute fabric showed balanced flame retardancy property (LOI value 34) with some loss in fabric tenacity (loss of tenacity is 14.5%). Treated fabric retained good fire retardant property after three consecutive washing. Treated fabric also possessed good rot resistance property as indicated by soil burial test and strength retention after 21 days soil burial was found to be 65%. It is found that of sodium stannate and boric acid combination by double bath process form a synergistic durable fire-retardant as well as rot resistant when impregnated on jute material, which is considerably greater than the use of either sodium stannate or boric acid alone. TGA, FTIR and SEM analysis are also reported to support the results and reaction mechanism.

  1. Capillary Electrophoresis Analysis of Organic Amines and Amino Acids in Saline and Acidic Samples Using the Mars Organic Analyzer

    Science.gov (United States)

    Stockton, Amanda M.; Chiesl, Thomas N.; Lowenstein, Tim K.; Amashukeli, Xenia; Grunthaner, Frank; Mathies, Richard A.

    2009-11-01

    The Mars Organic Analyzer (MOA) has enabled the sensitive detection of amino acid and amine biomarkers in laboratory standards and in a variety of field sample tests. However, the MOA is challenged when samples are extremely acidic and saline or contain polyvalent cations. Here, we have optimized the MOA analysis, sample labeling, and sample dilution buffers to handle such challenging samples more robustly. Higher ionic strength buffer systems with pKa values near pH 9 were developed to provide better buffering capacity and salt tolerance. The addition of ethylaminediaminetetraacetic acid (EDTA) ameliorates the negative effects of multivalent cations. The optimized protocol utilizes a 75 mM borate buffer (pH 9.5) for Pacific Blue labeling of amines and amino acids. After labeling, 50 mM (final concentration) EDTA is added to samples containing divalent cations to ameliorate their effects. This optimized protocol was used to successfully analyze amino acids in a saturated brine sample from Saline Valley, California, and a subcritical water extract of a highly acidic sample from the Río Tinto, Spain. This work expands the analytical capabilities of the MOA and increases its sensitivity and robustness for samples from extraterrestrial environments that may exhibit pH and salt extremes as well as metal ions.

  2. Uptake of BSH in M2R melanoma cells monitored by NMR spectroscopy

    International Nuclear Information System (INIS)

    Koudinova, N.; Elhanati, G.; Salomon, Y.; Bendel, P.

    2000-01-01

    The accumulation ratio of BSH, relative to that of boric acid, in M2R mouse melanoma cells, was measured using 11 B NMR of the cell extracts. The cells were incubated in growth medium for up to 24 h, in the presence of 0.8 mM boric acid and 0.25-1.5 mM BSH. The aqueous phase of the cellular extracts was re-suspended for NMR spectroscopy. The relative accumulation ratio of BSH/boric acid determined from 9 separate experiments was 0.45±0.09. (author)

  3. Universal nucleic acids sample preparation method for cells, spores and their mixture

    Science.gov (United States)

    Bavykin, Sergei [Darien, IL

    2011-01-18

    The present invention relates to a method for extracting nucleic acids from biological samples. More specifically the invention relates to a universal method for extracting nucleic acids from unidentified biological samples. An advantage of the presently invented method is its ability to effectively and efficiently extract nucleic acids from a variety of different cell types including but not limited to prokaryotic or eukaryotic cells and/or recalcitrant organisms (i.e. spores). Unlike prior art methods which are focused on extracting nucleic acids from vegetative cell or spores, the present invention effectively extracts nucleic acids from spores, multiple cell types or mixtures thereof using a single method. Important that the invented method has demonstrated an ability to extract nucleic acids from spores and vegetative bacterial cells with similar levels effectiveness. The invented method employs a multi-step protocol which erodes the cell structure of the biological sample, isolates, labels, fragments nucleic acids and purifies labeled samples from the excess of dye.

  4. Carbon Isotopic Ratios of Amino Acids in Stardust-Returned Samples

    Science.gov (United States)

    Elsila, Jamie E.; Glavin, Daniel P.; Dworkin, Jason P.

    2009-01-01

    NASA's Stardust spacecraft returned to Earth samples from comet 81P/Wild 2 in January 2006. Preliminary examinations revealed the presence of a suite of organic compounds including several amines and amino acids, but the origin of these compounds could not be identified. Here. we present the carbon isotopic ratios of glycine and E-aminocaproic acid (EACH), the two most abundant amino acids observed, in Stardust-returned foil samples measured by gas chromatography-combustion-isotope ratio crass spectrometry coupled with quadrupole mass spectrometry (GC-QMS/IRMS).

  5. An Optical Test Strip for the Detection of Benzoic Acid in Food

    Directory of Open Access Journals (Sweden)

    Fatimah Abu Bakar

    2011-07-01

    Full Text Available Fabrication of a test strip for detection of benzoic acid was successfully implemented by immobilizing tyrosinase, phenol and 3-methyl-2-benzothiazolinone hydrazone (MBTH onto filter paper using polystyrene as polymeric support. The sensing scheme was based on the decreasing intensity of the maroon colour of the test strip when introduced into benzoic acid solution. The test strip was characterized using optical fiber reflectance and has maximum reflectance at 375 nm. It has shown a highly reproducible measurement of benzoic acid with a calculated RSD of 0.47% (n = 10. The detection was optimized at pH 7. A linear response of the biosensor was obtained in 100 to 700 ppm of benzoic acid with a detection limit (LOD of 73.6 ppm. At 1:1 ratio of benzoic acid to interfering substances, the main interfering substance is boric acid. The kinetic analyses show that, the inhibition of benzoic is competitive inhibitor and the inhibition constant (Ki is 52.9 ppm. The activity of immobilized tyrosinase, phenol, and MBTH in the test strip was fairly sustained during 20 days when stored at 3 °C. The developed test strip was used for detection of benzoic acid in food samples and was observed to have comparable results to the HPLC method, hence the developed test strip can be used as an alternative to HPLC in detecting benzoic acid in food products.

  6. Perfluoroalkyl Acid Concentrations in Blood Samples Subjected to Transportation and Processing Delay.

    Science.gov (United States)

    Bach, Cathrine Carlsen; Henriksen, Tine Brink; Bossi, Rossana; Bech, Bodil Hammer; Fuglsang, Jens; Olsen, Jørn; Nohr, Ellen Aagaard

    2015-01-01

    In studies of perfluoroalkyl acids, the validity and comparability of measured concentrations may be affected by differences in the handling of biospecimens. We aimed to investigate whether measured plasma levels of perfluoroalkyl acids differed between blood samples subjected to delay and transportation prior to processing and samples with immediate processing and freezing. Pregnant women recruited at Aarhus University Hospital, Denmark, (n = 88) provided paired blood samples. For each pair of samples, one was immediately processed and plasma was frozen, and the other was delayed and transported as whole blood before processing and freezing of plasma (similar to the Danish National Birth Cohort). We measured 12 perfluoroalkyl acids and present results for compounds with more than 50% of samples above the lower limit of quantification. For samples taken in the winter, relative differences between the paired samples ranged between -77 and +38% for individual perfluoroalkyl acids. In most cases concentrations were lower in the delayed and transported samples, e.g. the relative difference was -29% (95% confidence interval -30; -27) for perfluorooctane sulfonate. For perfluorooctanoate there was no difference between the two setups [corresponding estimate 1% (0, 3)]. Differences were negligible in the summer for all compounds. Transport of blood samples and processing delay, similar to conditions applied in some large, population-based studies, may affect measured perfluoroalkyl acid concentrations, mainly when outdoor temperatures are low. Attention to processing conditions is needed in studies of perfluoroalkyl acid exposure in humans.

  7. X-ray fluorescence analysis of erbium oxide/oxalate for rare earth impurities

    International Nuclear Information System (INIS)

    Chandola, L.C.; Khanna, P.P.; Thomas, A.

    1981-01-01

    A method for the determination of Tb, Dy, Ho, Tm, Yb, Lu and Y oxides in Er 2 O 3 is described. 450 mg sample in the oxalate form is mixed with 150 mg boric acid binding material and pressed into a 1.25 inch diameter pellet over a supporting pellet of boric acid. The sample is then irradiated by X-rays from a tungsten tube and the fluorescent X-rays are dispersed by a LiF (200) crystal in a Philips PW 1220 semiautomatic X-ray fluorescence spectrometer. The intensities of characteristic X-rays of the impurity elements are measured by a flow proportional counter for all elements except yttrium for which the intensities are measured by a scintillation counter. The lowest determination limit is 0.005% for all impurities except for Yb for which it is 0.01%. Calculations for theoretical detection limit are given. (author)

  8. The Impact Of The MCU Life Extension Solvent On Sludge Batch 8 Projected Operating Windows

    International Nuclear Information System (INIS)

    Peeler, D. K.; Edwards, T. B.; Stone, M. E.

    2013-01-01

    As a part of the Actinide Removal Process (ARP)/Modular Caustic Side Solvent Extraction Unit (MCU) Life Extension Project, a next generation solvent (NGS) and a new strip acid will be deployed. The strip acid will be changed from dilute nitric acid to dilute boric acid (0.01 M). Because of these changes, experimental testing or evaluations with the next generation solvent are required to determine the impact of these changes (if any) to Chemical Process Cell (CPC) activities, glass formulation strategies, and melter operations at the Defense Waste Processing Facility (DWPF). The introduction of the dilute (0.01M) boric acid stream into the DWPF flowsheet has a potential impact on glass formulation and frit development efforts since B2O3 is a major oxide in frits developed for DWPF. Prior knowledge of this stream can be accounted for during frit development efforts but that was not the case for Sludge Batch 8 (SB8). Frit 803 has already been recommended and procured for SB8 processing; altering the frit to account for the incoming boron from the strip effluent (SE) is not an option for SB8. Therefore, the operational robustness of Frit 803 to the introduction of SE including its compositional tolerances (i.e., up to 0.0125M boric acid) is of interest and was the focus of this study. The primary question to be addressed in the current study was: What is the impact (if any) on the projected operating windows for the Frit 803 - SB8 flowsheet to additions of B2O3 from the SE in the Sludge Receipt and Adjustment Tank (SRAT)? More specifically, will Frit 803 be robust to the potential compositional changes occurring in the SRAT due to sludge variation, varying additions of ARP and/or the introduction of SE by providing access to waste loadings (WLs) of interest to DWPF? The Measurement Acceptability Region (MAR) results indicate there is very little, if any, impact on the projected operating windows for the Frit 803 - SB8 system regardless of the presence or absence of

  9. Micropropagação de duas espécies frutíferas, em meio de cultura DSD1, modificado com fontes de boro e zinco Micropropagation of two fruit tree species on dsd1 culture medium modified with boric acid and zinc sulfate

    Directory of Open Access Journals (Sweden)

    Fabíola Villa

    2009-04-01

    H adjusted to 6.4 before the sterilization at 121ºC and 1 atm per 20 minutes. The treatments consisted of blackberry plants cv. Tupy, the grapevine rootstock 'Kobber' and concentrations of boric acid (0; 1.0; 2.0, and 4.0 mg L-1 and zinc sulfate (0; 1.0; 2.0, and 4.0 mg L-1, mixed in all possible combinations. Nodal segments of in vitro cultivated plants were excised and inoculated in tubes with 15 mL culture medium. After that, the tubes were transferred to a growth room at 27 ± 1ºC, irradiance of 35 mol.m-2.s-1 and photoperiod of 16 hours. The experiment was arranged in a completely randomized design, using four replications with 12 plants each. After 70 days of in vitro cultivation it was verified that the best results for the micropropagation of blackberry cv. Tupy (Rubus sp. were obtained in the absence of boric acid and zinc sulfate mixed in the DSD1culture medium. With 4.0 mg L-1 boric acid added to the culture medium higher number of leaves and length of roots of the grapevine rootstock 'Kobber' (Vitis sp. was observed.

  10. Characteristics of β-glucosidase production by Paecilomyces variotii ...

    African Journals Online (AJOL)

    This study reports the potential application of Paecilomyces variotii immobilized in calcium alginate beads as a sensing element in the analysis of boric acid. In the presence of boric acid, β-glucosidase production of P. variotii was inhibited and the changes of β-glucosidase concentration were correlated to the ...

  11. X-ray fluorescence analysis of terbium oxide for rare earth impurities

    International Nuclear Information System (INIS)

    Chandola, L.C.; Machado, I.J.; Mohile, A.N.

    1975-01-01

    A method for the determination of Sm 2 O 3 , Eu 2 O 3 , Gd 2 O 3 , Dy 2 O 3 , Ho 2 O 3 and Y 2 O 3 in terbium oxide is described. The sample is converted to terbium oxalate, mixed with boric acid binder in the ratio 2:1, pelleted at a pressure of 20 tons over a boric acid backing pellet and irradiated with x-rays from a tungsten tube operated by Philips PW 1140 generator. The secondary x-rays thus generated are analysed by a LiF (200) crystal in Philips PW 1220 x-ray fluorescence spectrometer using suitable detectors. The minimum determination limit (MDL) is 0.01% for all rare earth oxides determined except for Y 2 O 3 for which it is 0.005%. (author)

  12. Enrichment of boron 10

    International Nuclear Information System (INIS)

    Coutinho, C.M.M.; Rodrigues Filho, J.S.R.; Umeda, K.; Echternacht, M.V.

    1990-01-01

    A isotopic separation pilot plant with five ion exchange columns interconnected in series were designed and built in the IEN. The columns are charged with a strong anionic resin in its alkaline form. The boric acid solution is introduced in the separation columns until it reaches a absorbing zone length which is sufficient to obtain the desired boron-10 isotopic concentration. The boric acid absorbing zone movement is provided by the injection of a diluted hydrochloric acid solution, which replace the boric acid throughout the columns. The absorbing zone equilibrium length is proportional to its total length. The enriched boron-10 and the depleted boron are located in the final boundary and in the initial position of the absorbing zones, respectively. (author)

  13. Boric oxide or boric acid sintering aid for sintering ceramics

    International Nuclear Information System (INIS)

    Lawler, H.A.

    1979-01-01

    The invention described relates to the use of liquid sintering aid in processes involving sintering of ceramic materials to produce dense, hard articles having industrial uses. Although the invention is specifically discussed in regard to compositions containing silicon carbide as the ceramic material, other sinterable carbides, for example, titanium carbide, may be utilized as the ceramic material. A liquid sintering aid for densifying ceramic material is selected from solutions of H 3 BO 3 , B 2 O 3 and mixtures of these solutions. In sintering ceramic articles, e.g. silicon carbide, a shaped green body is formed from a particulate ceramic material and a resin binder, and the green body is baked at a temperature of 500 to 1000 0 C to form a porous body. The liquid sintering aid of B 2 O 3 and/or H 3 BO 3 is then dispersed through the porous body and the treated body is sintered at a temperature of 1900 to 2200 0 C to produce the sintered ceramic article. (U.K.)

  14. Impact of impregnation with boron compounds on combustion ...

    African Journals Online (AJOL)

    This study examined the impacts of varnishing after impregnation with boron compounds on combustion properties of oriental beech. The test samples prepared from oriental beech (Fagus orientalis Lipsky) wood were impregnated according to ASTM D 1413–76–99 with boric acid (Ba) or borax (Bx) using a vacuum ...

  15. Tank 12H Acidic Chemical Cleaning Sample Analysis And Material Balance

    International Nuclear Information System (INIS)

    Martino, C. J.; Reboul, S. H.; Wiersma, B. J.; Coleman, C. J.

    2013-01-01

    A process of Bulk Oxalic Acid (BOA) chemical cleaning was performed for Tank 12H during June and July of 2013 to remove all or a portion of the approximately 4400 gallon sludge heel. Three strikes of oxalic acid (nominally 4 wt % or 2 wt %) were used at 55 deg C and tank volumes of 96- to 140-thousand gallons. This report details the sample analysis of a scrape sample taken prior to BOA cleaning and dip samples taken during BOA cleaning. It also documents a rudimentary material balance for the Tank 12H cleaning results

  16. The Impact Of The Mcu Life Extension Solvent On Dwpf Glass Formulation Efforts

    International Nuclear Information System (INIS)

    Peeler, D.; Edwards, T.

    2011-01-01

    As a part of the Actinide Removal Process (ARP)/Modular Caustic Side Solvent Extraction Unit (MCU) Life Extension Project, a next generation solvent (NG-CSSX), a new strip acid, and modified monosodium titanate (mMST) will be deployed. The strip acid will be changed from dilute nitric acid to dilute boric acid (0.01 M). Because of these changes, experimental testing with the next generation solvent and mMST is required to determine the impact of these changes in 512-S operations as well as Chemical Process Cell (CPC), Defense Waste Processing Facility (DWPF) glass formulation activities, and melter operations at DWPF. To support programmatic objectives, the downstream impacts of the boric acid strip effluent (SE) to the glass formulation activities and melter operations are considered in this study. More specifically, the impacts of boric acid additions to the projected SB7b operating windows, potential impacts to frit production temperatures, and the potential impact of boron volatility are evaluated. Although various boric acid molarities have been reported and discussed, the baseline flowsheet used to support this assessment was 0.01M boric acid. The results of the paper study assessment indicate that Frit 418 and Frit 418-7D are robust to the implementation of the 0.01M boric acid SE into the SB7b flowsheet (sludge-only or ARP-added). More specifically, the projected operating windows for the nominal SB7b projections remain essentially constant (i.e., 25-43 or 25-44% waste loading (WL)) regardless of the flowsheet options (sludge-only, ARP added, and/or the presence of the new SE). These results indicate that even if SE is not transferred to the Sludge Receipt and Adjustment Tank (SRAT), there would be no need to add boric acid (from a trim tank) to compositionally compensate for the absence of the boric acid SE in either a sludge-only or ARP-added SB7b flowsheet. With respect to boron volatility, the Measurement Acceptability Region (MAR) assessments also

  17. Development of automatic high-concentration boron measurement technique; Konodo hoso jido sokutei gijutsu no kaihatsu

    Energy Technology Data Exchange (ETDEWEB)

    Maeda, T.; Honda, S.; Ito, A. [Kyushu Electric Power Co. Inc., Fukuoka (Japan)

    1997-03-01

    The technology that can automatically measure the boron concentration in boric acid water was developed. A high-concentration boric acid solution must be held at a high temperature to prevent the deposition. Skill and precision ({plus_minus}0.2 to 0.3% for 10 to 2500 ppm as boron concentration, and {plus_minus}2 to 3% for 2500 to 25,000 ppm) are required to analyze the boric acid solution manually. In theory, the boron concentration in a wide range can be measured, and boron has a constant-temperature function. A density hydrometer method that facilitates the treatment and calibration in high precision and at low cost was chosen. The vibration period generated when vibration is given to the solution specimen put in a U-tube is higher as the density is lower. On the basis of this theory, the density of a specimen can be obtained according to the relation with the same data of the known-concentration boric acid water. The high-concentration boric acid water that cannot be measured by the existing boron densitometer can be measured directly. It can also be measured in a low-concentration area. The technique can be used in a laboratory as the simplified method that is replaced by the current manual analysis. The reduction effect of analytical chemical`s waste liquid can also be expected. In the electric power industry, automated equipment is required for high efficiency and labor saving. 13 figs., 3 tabs.

  18. Effects of radiation and impurities on gaseous iodine behavior in a containment vessel

    International Nuclear Information System (INIS)

    Takahashi, Masato; Watanabe, Atsushi; Hashimoto, Takashi

    2000-01-01

    In order to estimate the effect of impurities and radiation on gaseous iodine behavior in containment vessel, NUPEC has improved IMPAIR-3 code developed by PSI. Several modifications on the iodine oxidation by radiolysis and the production of nitric acid, the existence of boric acid, and the reaction of silver particle with iodine were newly added in evaluating the effect of radiolysis and impurities. pH change resulting from presence of boric acid, nitric acid production by radiolysis of air, and sodium hydroxide addition by AM operation, was also considered. The code verification for pH change was performed using the RTF experimental results. Additionally, the effects of boric acid and silver impurities on gaseous iodine behavior were evaluated by the sensitivity analysis. As a result, the experimental results of iodine concentration transient under pH change were well simulated. The following results were also obtained from the sensitive analysis. The gaseous iodine behavior was not affected by the existence of boric acid. In the case of silver existence in liquid phase, the gaseous iodine concentration rapidly decreased because a large amount of iodine changed into AgI species in liquid phase. The restraint effect of silver on gaseous iodine, production was larger than that of pH change. (author)

  19. Limited oxygen index levels of impregnated Scots pine wood

    International Nuclear Information System (INIS)

    Tomak, Eylem Dizman; Cavdar, Ayfer Donmez

    2013-01-01

    Highlights: • Scots pine samples were treated with 4 wood preservatives with various concentrations. • Limited oxygen index level was evaluated both for leached and un-leached samples. • All treatments improved fire retardance of samples despite some chemicals leached out. • Samples treated with fireproof agent showed the best results. • LOI of samples treated with boron powder and silicon oil was not changed by leaching. - Abstract: In this study, effect of various concentrations of boron powder, mixture of boric acid and borax, fireproof agent based on liquid blend of limestone, and silicon oil on limited oxygen index levels (LOI) of S. pine wood was investigated. Wood samples were first vacuum treated with the preservatives, and then were subjected to leaching procedure. Samples treated with fireproof agent showed the best results for improving the fire retardancy of wood, furthermore, samples treated with 25%, 50% and 100% of the solution did not burn. Leaching did not considerably change the LOI of wood samples treated with boron powder and silicon oil; however, LOI levels of samples treated with the mixture of boric acid and borax and fireproof agent were affected by leaching procedure probably arising those preservatives did not chemically bond to main wood components. All treatments improved fire retardancy of samples despite some amount of preservatives leached out from wood

  20. Limited oxygen index levels of impregnated Scots pine wood

    Energy Technology Data Exchange (ETDEWEB)

    Tomak, Eylem Dizman, E-mail: eylemdizman@yahoo.com [Forest Industry Engineering Department, Faculty of Forestry, Bursa Technical University, 16200 Bursa (Turkey); Cavdar, Ayfer Donmez [Interior Architecture Department, Faculty of Architecture, Karadeniz Technical University, 61080 Trabzon (Turkey)

    2013-12-10

    Highlights: • Scots pine samples were treated with 4 wood preservatives with various concentrations. • Limited oxygen index level was evaluated both for leached and un-leached samples. • All treatments improved fire retardance of samples despite some chemicals leached out. • Samples treated with fireproof agent showed the best results. • LOI of samples treated with boron powder and silicon oil was not changed by leaching. - Abstract: In this study, effect of various concentrations of boron powder, mixture of boric acid and borax, fireproof agent based on liquid blend of limestone, and silicon oil on limited oxygen index levels (LOI) of S. pine wood was investigated. Wood samples were first vacuum treated with the preservatives, and then were subjected to leaching procedure. Samples treated with fireproof agent showed the best results for improving the fire retardancy of wood, furthermore, samples treated with 25%, 50% and 100% of the solution did not burn. Leaching did not considerably change the LOI of wood samples treated with boron powder and silicon oil; however, LOI levels of samples treated with the mixture of boric acid and borax and fireproof agent were affected by leaching procedure probably arising those preservatives did not chemically bond to main wood components. All treatments improved fire retardancy of samples despite some amount of preservatives leached out from wood.

  1. Highly simplified lateral flow-based nucleic acid sample preparation and passive fluid flow control

    Science.gov (United States)

    Cary, Robert E.

    2015-12-08

    Highly simplified lateral flow chromatographic nucleic acid sample preparation methods, devices, and integrated systems are provided for the efficient concentration of trace samples and the removal of nucleic acid amplification inhibitors. Methods for capturing and reducing inhibitors of nucleic acid amplification reactions, such as humic acid, using polyvinylpyrrolidone treated elements of the lateral flow device are also provided. Further provided are passive fluid control methods and systems for use in lateral flow assays.

  2. Highly simplified lateral flow-based nucleic acid sample preparation and passive fluid flow control

    Energy Technology Data Exchange (ETDEWEB)

    Cary, Robert B.

    2018-04-17

    Highly simplified lateral flow chromatographic nucleic acid sample preparation methods, devices, and integrated systems are provided for the efficient concentration of trace samples and the removal of nucleic acid amplification inhibitors. Methods for capturing and reducing inhibitors of nucleic acid amplification reactions, such as humic acid, using polyvinylpyrrolidone treated elements of the lateral flow device are also provided. Further provided are passive fluid control methods and systems for use in lateral flow assays.

  3. Selective removal of phosphate for analysis of organic acids in complex samples.

    Science.gov (United States)

    Deshmukh, Sandeep; Frolov, Andrej; Marcillo, Andrea; Birkemeyer, Claudia

    2015-04-03

    Accurate quantitation of compounds in samples of biological origin is often hampered by matrix interferences one of which occurs in GC-MS analysis from the presence of highly abundant phosphate. Consequently, high concentrations of phosphate need to be removed before sample analysis. Within this context, we screened 17 anion exchange solid-phase extraction (SPE) materials for selective phosphate removal using different protocols to meet the challenge of simultaneous recovery of six common organic acids in aqueous samples prior to derivatization for GC-MS analysis. Up to 75% recovery was achieved for the most organic acids, only the low pKa tartaric and citric acids were badly recovered. Compared to the traditional approach of phosphate removal by precipitation, SPE had a broader compatibility with common detection methods and performed more selectively among the organic acids under investigation. Based on the results of this study, it is recommended that phosphate removal strategies during the analysis of biologically relevant small molecular weight organic acids consider the respective pKa of the anticipated analytes and the detection method of choice. Copyright © 2015 Elsevier B.V. All rights reserved.

  4. Perfluoroalkyl Acid Concentrations in Blood Samples Subjected to Transportation and Processing Delay

    DEFF Research Database (Denmark)

    Bach, Cathrine Carlsen; Henriksen, Tine Brink; Bossi, Rossana

    2015-01-01

    and transportation prior to processing and samples with immediate processing and freezing. METHODS: Pregnant women recruited at Aarhus University Hospital, Denmark, (n = 88) provided paired blood samples. For each pair of samples, one was immediately processed and plasma was frozen, and the other was delayed...... and transported as whole blood before processing and freezing of plasma (similar to the Danish National Birth Cohort). We measured 12 perfluoroalkyl acids and present results for compounds with more than 50% of samples above the lower limit of quantification. RESULTS: For samples taken in the winter, relative...... differences between the paired samples ranged between -77 and +38% for individual perfluoroalkyl acids. In most cases concentrations were lower in the delayed and transported samples, e.g. the relative difference was -29% (95% confidence interval -30; -27) for perfluorooctane sulfonate. For perfluorooctanoate...

  5. Scoria analysis by X-ray fluorescence with briquet

    International Nuclear Information System (INIS)

    Silva, G.R. da; Albert, P.E.

    1987-01-01

    The sample of scoria is triturated, using boric acid as agglomerative. The briquets are analyzed by X-ray quantometry, establishing the proportions of SiO 2 , P 2 O 5 , S, Cr 2 O 3 , V 2 O 5 , TiO 2 , Al 2 O 3 , Mg O, Ca O, FeO and their basicity. The calibration curves are prepared with standard scoria samples, by chemical analysis. (C.G.C.) [pt

  6. Advanced boron soaking procedure for steam generators

    International Nuclear Information System (INIS)

    Ueno, T.; Tsuge, A.; Kawanishi, K.; Ochi, T.; Kadokami, E.

    1991-01-01

    An experimental study on boric acid penetration into tube to tube-support-plate crevices and Inter-Granular-Attack (hereinafter called 'IGA') cracks in crevices has been performed to obtain the optimum boric acid soaking procedure in operating steam generators with IGA. The penetration rate into the crevice is closely related to various parameters such as heat flux, crevice gap, and porosity of the sludge deposited in crevices. Two experimental crevice models were set up. One was of the packed crevice type; crevice gap is completely packed by sludge, and the other was of the open crevice type; crevice gap is not packed, but reduced by sludge. The porosity of the crevice varied from 100% open porosity to the highly sludge packed porosity of 10∼20%. The relation between heat flux and boric acid penetration rate of the packed crevice type was investigated. For the open crevice type, from the viewpoint that boric acid penetration into the dryout region produces no effects, tube wall superheat in the crevice was measured in order to obtain the dryout heat flux. And it was investigated the boron in IGA cracks using Ion Micro Analysis in order to confirm existence of an anticorrosive film in IGA propagation. The optimum reactor power for effective boric acid penetration onto the tube surface and into the IGA cracks within the tube to tube-support-plate crevice was found to be about a 5% and 30% power level, which are applicable to both the packed and open crevice type. (author)

  7. Leaching of nuclear power reactor wastes forms

    International Nuclear Information System (INIS)

    Endo, L.S.; Villalobos, J.P.; Miyamoto, H.

    1986-01-01

    The leaching tests for power reactor wastes carried out at IPEN/CNEN-SP are described. These waste forms consist mainly of spent resins and boric acid concentrates solidified in ordinary Portland cement. All tests were conducted according to the ISO and IAEA recommendations. 3 years leaching results are reported, determining cesium and strontium diffusivity coefficients for boric acid waste form and ion-exchange resins. (Author) [pt

  8. The determination, by x-ray-fluorescence spectrometry, of gold, silver, and base metals on activated carbon

    International Nuclear Information System (INIS)

    Wall, G.; Jacobs, J.J.; Dixon, K.

    1980-01-01

    The method proposed involves ashing of the sample at a low temperature in a muffle furnace, mixing of the ash with alumina and boric acid in a Siebtechnik mill, and briquetting of the mixture. The elements are measured in the briquette by the use of x-ray fluorescence spectrometry. The detailed laboratory method is given in an appendix [af

  9. Genomic regions associated with bovine milk fatty acids in both summer and winter milk samples

    NARCIS (Netherlands)

    Bouwman, A.C.; Visker, M.H.P.W.; Arendonk, van J.A.M.; Bovenhuis, H.

    2012-01-01

    Background - In this study we perform a genome-wide association study (GWAS) for bovine milk fatty acids from summer milk samples. This study replicates a previous study where we performed a GWAS for bovine milk fatty acids based on winter milk samples from the same population. Fatty acids from

  10. Separation of glycols from dilute aqueous solutions via complexation with boronic acids

    Energy Technology Data Exchange (ETDEWEB)

    Randel, L.A.; King, C.J.

    1991-07-01

    This work examines methods of separating low molecular weight glycols from dilute aqueous solution. Extraction into conventional solvents is generally not economical, since, in the literature reviewed, distribution ratios for the two- to four-carbon glycols are all less than one. Distribution ratios can be increased, however, by incorporating into the organic phase an extracting agent that will complex with the solute of interest. The extracting agent investigated in this work is 3-nitrophenylboronic acid (NPBA). NPBA, a boric acid derivative, reversibly complexes with many glycols. The literature on complexation of borate and related compounds with glycols, including mechanistic data, measurement techniques, and applications to separation processes, provides information valuable for designing experiments with NPBA and is reviewed herein. 88 refs., 15 figs., 24 tabs.

  11. Evaluation of a Solid Dispersion of Curcumin With Polyvinylpyrrolidone and Boric Acid Against Salmonella Enteritidis Infection and Intestinal Permeability in Broiler Chickens: A Pilot Study

    Directory of Open Access Journals (Sweden)

    Daniel Hernandez-Patlan

    2018-06-01

    Full Text Available In the present study, in vitro assays were conducted to evaluate the solubility of curcumin (CUR alone or with polyvinylpyrrolidone (PVP at different pH, as well as its permeability in Caco-2 cells. Results confirmed that the solid dispersion of CUR with PVP (CUR/PVP at a 1:9 ratio, significantly increased (P < 0.05 solubility and permeability compared to CUR alone. Then, the antimicrobial activity of CUR/PVP, boric acid (BA, and a combination of 0.5% CUR/PVP and 0.5% BA (CUR/PVP-BA against Salmonella Enteritidis (SE was determined using an in vitro digestion model that simulates crop, proventriculus, and intestine. The results revealed that in the proventriculus and intestinal compartments significant reductions of SE were observed in all the experimental treatments, but 1% BA eliminated SE in the intestinal compartment and CUR/PVP-BA showed a synergistic effect on antimicrobial activity against SE. To complement these findings, two independent in vivo trials were conducted to determine the effect of 0.1% CUR/PVP; 0.1% BA; or the combination of 0.05% CUR/PVP (1:9 ratio and 0.05% BA (CUR/PVP-BA on the antimicrobial activity against SE, intestinal permeability and inflammatory responses in broiler chickens. BA at 0.1% had no significant in vivo effects against SE. However, the combination of 0.05% BA and 0.05% CUR/PVP and 0.05% BA was sufficient to reduce crop and intestinal SE colonization in broiler chickens in two independent trials, confirming the synergic effect between them. A similar antimicrobial impact against SE intestinal colonization was observed in chickens treated with 0.1% CUR/PVP at a 1:9 ratio, which could be due to the increase in solubility of CUR by PVP. Furthermore, 0.1% CUR/PVP reduced the intestinal permeability of FITC-d and total intestinal IgA, as well as increase the activity of SOD when compared to control, while, CUR/PVP-BA only decreased SOD activity. Further studies to confirm and expand the in vivo results obtained

  12. Acid digestion of geological and environmental samples using open-vessel focused microwave digestion.

    Science.gov (United States)

    Taylor, Vivien F; Toms, Andrew; Longerich, Henry P

    2002-01-01

    The application of open vessel focused microwave acid digestion is described for the preparation of geological and environmental samples for analysis using inductively coupled plasma-mass spectrometry (ICP-MS). The method is compared to conventional closed-vessel high pressure methods which are limited in the use of HF to break down silicates. Open-vessel acid digestion more conveniently enables the use of HF to remove Si from geological and plant samples as volatile SiF4, as well as evaporation-to-dryness and sequential acid addition during the procedure. Rock reference materials (G-2 granite, MRG-1 gabbros, SY-2 syenite, JA-1 andesite, and JB-2 and SRM-688 basalts) and plant reference materials (BCR and IAEA lichens, peach leaves, apple leaves, Durham wheat flour, and pine needles) were digested with results comparable to conventional hotplate digestion. The microwave digestion method gave poor results for granitic samples containing refractory minerals, however fusion was the preferred method of preparation for these samples. Sample preparation time was reduced from several days, using conventional hotplate digestion method, to one hour per sample using our microwave method.

  13. [Microeukaryotic biodiversity in the waste ore samples surrounding an acid mine drainage lake].

    Science.gov (United States)

    Li, Si-Yuan; Hao, Chun-Bo; Wang, Li-Hua; Lü, Zheng; Zhang, Li-Na; Liu, Ying; Feng, Chuan-Ping

    2013-10-01

    The abandoned mineral samples were collected in an acid mine drainage area in Anhui Province. Molecular ecological methods were used to construct 18S rDNA clone libraries after analyzing the main physicochemical parameters, and then the microeukaryotic diversity and community structure in the acid mine drainage area were studied. The results showed that the region was strongly acidic (pH <3), and the concentrations of Fe, SO2-(4), P, NO-(3) -N showed the same trend, all higher in the bare waste ore samples PD and 1 M than in the vegetation covered samples LW and XC. Four eukaryotic phyla were detected in the abandoned mineral samples: Ascomycota, Basidiomycota, Glomeromycota and Arthropoda. Glomeromycota can form an absolute symbiotic relationship with the plant, and it was a key factor for early plant to adapt the terrestrial environment. The biodiversity of the vegetation covered samples LW and XC, which contained Glomeromycota, was much higher than that of the bare abandoned rock samples PD and 1 M. Moreover, many sequences in the libraries were closely related to some isolated strains, which are tolerant to low pH and heavy metals, such as Penicillium purpurogenum, Chaetothyriales sp. and Staninwardia suttonii.

  14. 3M"T"M neutron quench. Compounds with substantial water solubility and boron content

    International Nuclear Information System (INIS)

    Cook, Kevin S.; Blake, Alex B.; Neef, C. Jody

    2014-01-01

    Of the two naturally occurring isotopes of boron ("1"1B 80%, "1"0B 20%), "1"0B is a good neutron absorber with a thermal neutron absorption cross section of ∼3800 barns. The ability to absorb thermal neutrons while producing benign reaction products makes boron an ideal atom to aid in the control and arrest of the fission reaction in nuclear power reactors. In current practice, boric acid and sodium pentaborate are commonly used as neutron absorbers in the water regime of active and passive safety systems. 3M"T"M Neutron Quench compounds have been developed to be applied in situations where criticality control needs exceed normal control methods. In this type of situation these compounds have several advantages over commonly used neutron absorbers like boric acid: Boron Content; compounds contain up to 80 wt% boron compared to 16 wt% for boric acid and sodium pentaborate. Solubility; >16 g B/100 g solution compared to 0.6 g B/100 g solution for boric acid at 25°C. pH neutrality; compounds demonstrate pH neutrality even in concentrated solutions. Thermal Stability; Compounds are stable as solids at temperatures greater than 500°C. Corrosiveness; Electrochemical corrosion rate studies have indicated that these compounds are significantly less corrosive than boric acid. Use of 3M"T"M Neutron Quench can lead to reduction in emergency shutdown pool size, reduce or remove the necessity for pool heating and heat tracing of lines, allow for more rapid introduction of the absorber in emergency situations or be used in other applications where significant neutron control is necessary. (author)

  15. Optimization of crosslinked poly(vinyl alcohol) nanocomposite films for mechanical properties.

    Science.gov (United States)

    Rouhi, Milad; Razavi, Seyed Hadi; Mousavi, Seyed Mohammad

    2017-02-01

    The effects of glycerol, bacterial cellulose nanocrystal (BCNC) and boric acid concentrations on the mechanical properties of PVA based films, including ultimate tensile strength (UTS), elongation at break (EAB), tensile Young's modulus (TYM), tensile toughness to break (TT), ultimate puncture strength (UPS), puncture deformation (PD), puncture Young's modulus (PYM) and puncture toughness to break (PT), were scrutinized using a response surface methodology-central composite rotatable design (RSM-CCRD). Second-order polynomial models with high R 2 values ranging from 0.945 to 0.977 were developed for the studied responses using multiple linear regression analysis. The models showed the maximum UTS (72.84MPa), EAB (293.43%), UPS (4.64MPa) and PD (31.80%) could be achieved at 13.89% glycerol concentration, 5.00% BCNC concentration and a boric acid content of 1.96%. The predicted values for optimum conditions were in good agreement with experimental data. Fourier-transform infrared spectroscopy (FTIR) analysis confirmed the formation of intramolecular and intermolecular hydrogen and ether crosslinkages in PVA and/or BCNC chains when boric acid is applied. Results showed that PVA/BCNC nanocomposite films plasticized with glycerol and crosslinked with boric acid showed appropriate mechanical properties that made them suitable as a disposable packaging film. Copyright © 2016 Elsevier B.V. All rights reserved.

  16. Chemical enhancement of crevice flushing: Volume 2, Data documentation: Final report

    International Nuclear Information System (INIS)

    Baum, A.J.; Prestegiacomo, J.B.

    1987-06-01

    The primary objective of this project was to evaluate the effect of various chemical additives on enhancing the hideout return produced during tubesheet crevice flushing operations in PWR steam generators. Secondary objectives included determining if flushing was an effective means of introducing a corrosion inhibitor into deep tubesheet crevices, and evaluating the effects of different degrees of crevice restriction, different initial crevice chemistries, and different flushing processes. Testing was unable to identify a single additive formulation which increased the flushing effectiveness for all degrees of crevice restriction considered. Testing did reveal that a combination of surfactant (Surfynol 104) and boric acid enhances the flushing effectiveness in tests with moderately restricted crevices. Although cleaning agents were found to increase the flushing effectiveness in tests with extensively restricted crevices, potential corrosion concerns and relatively high contaminant (sodium) levels could discourage their use. However, the testing demonstrated that flushing was an effective means of accumulating a corrosion inhibitor, such as boric acid, in deep tubesheet crevices. Companion testing also indicated that boric acid which accumulated in a tubesheet crevice during crevice flushing was likely to remain in the crevice during subsequent power operation. Consequently, use of boric acid as an additive in tubesheet crevice flushing operations is strongly recommended

  17. Composition and method for coke retardant during hydrocarbon processing

    International Nuclear Information System (INIS)

    Reid, D.K.

    1988-01-01

    A process is described for inhibiting the formation and deposition of filamentous coke on metallic surfaces in contact with a hydrocarbon having a temperature of 600 0 -1300 0 F which comprises adding to the hydrocarbon a sufficient amount for the purpose of a boron compound selected from the group of boron oxide compounds, boric acid and metal borides, with the proviso that when boric acid is used, it is substantially free of water

  18. Effect of boron compounds on the thermal and combustion properties of wood-plastic composites

    OpenAIRE

    Altuntaş, Ertuğrul; Karaoğul, Eyyup; Alma, Mehmet Hakkı

    2017-01-01

    In this study, the thermal properties and fire resistancesof the wood plastic composites produced with waste lignocellulosic materialswere investigated. For this purpose, lignocellulosic waste, high densitypolyethylene, (HDPE) sodium borate (borax) and boric acid was used to producethe wood-plastic composites. A twin-screw extruder was used during theproduction of the wood plastic composites. The produced composite granule waspressed at 175 °C hot press. The effects of boric acid and borax ad...

  19. Bituminization of simulated PWR type reactor wastes, boric evaporator bottons and ion exchange resins, carried out in CNEN/SP using commercial bitumen available in the Brazilian market

    International Nuclear Information System (INIS)

    Grosche Filho, C.E.; Chandra, U.

    1986-01-01

    The first results of the study of bituminization of simulated PWR wastes, boric evaporator bottons and spent ion-exclange resins (OH - , H + ) and incinerated ash-wates are presented and discussed. The study consisted of characterization of the commercial bitumen, locally available and bitumen wastes products of varying whight compositions. The characterization was carried out using standard analysis methods of ABNT and ASTM, and included measurement of, penetration, softening point and flash point. In addition, the bitumen samples were analized for their resin and asphaltene contents. For leaching studies, wastes products of bitumen and resin loaded with 134 Cs were utilized. The method used was according to the ISO norms. The simulation of the industrial process was carried out using an extruder-evaporator typically used in the plastic industries offered by Industria de Maquinas Miotto Ltda., Sao Bernardo do Campo - SP. (Author) [pt

  20. Concurrent Lactic and Volatile Fatty Acid Analysis of Microbial Fermentation Samples by Gas Chromatography with Heat Pre-treatment.

    Science.gov (United States)

    Darwin; WipaCharles; Cord-Ruwisch, Ralf

    2018-01-01

    Organic acid analysis of fermentation samples can be readily achieved by gas chromatography (GC), which detects volatile organic acids. However, lactic acid, a key fermentation acid is non-volatile and can hence not be quantified by regular GC analysis. However the addition of periodic acid to organic acid samples has been shown to enable lactic acid analysis by GC, as periodic acid oxidizes lactic acid to the volatile acetaldehyde. Direct GC injection of lactic acid standards and periodic acid generated inconsistent and irreproducible peaks, possibly due to incomplete lactic acid oxidation to acetaldehyde. The described method is developed to improve lactic acid analysis by GC by using a heat treated derivatization pre-treatment, such that it becomes independent of the retention time and temperature selection of the GC injector. Samples containing lactic acid were amended by periodic acid and heated in a sealed test tube at 100°C for at least 45 min before injecting it to the GC. Reproducible and consistent peaks of acetaldehyde were obtained. Simultaneous determination of lactic acid, acetone, ethanol, butanol, volatile fatty acids could also be accomplished by applying this GC method, enabling precise and convenient organic acid analysis of biological samples such as anaerobic digestion and fermentation processes. © The Author 2017. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  1. Metalworking and machining fluids

    Science.gov (United States)

    Erdemir, Ali; Sykora, Frank; Dorbeck, Mark

    2010-10-12

    Improved boron-based metal working and machining fluids. Boric acid and boron-based additives that, when mixed with certain carrier fluids, such as water, cellulose and/or cellulose derivatives, polyhydric alcohol, polyalkylene glycol, polyvinyl alcohol, starch, dextrin, in solid and/or solvated forms result in improved metalworking and machining of metallic work pieces. Fluids manufactured with boric acid or boron-based additives effectively reduce friction, prevent galling and severe wear problems on cutting and forming tools.

  2. Method for preparation of borax decahydrate

    International Nuclear Information System (INIS)

    Dujnedenko, V.I.; Chumaevskij, V.A.; Kovalev, A.S.; Gabova, E.L.; Suvorova, M.R.; Smirnova, V.G.; Smirnov, A.S.

    1990-01-01

    A highly productive method of borax decahydrate preparation, consisting in the mixing of boric acid, soda and mother solution at the temperature not exceeding 40 deg is described. The mixture is supplied to borax circulating solution at the temperature of 85-95 deg. After crystallization borax decahydrate is isolated from mother solution and solution is directed for mixing with boric acid and soda. The given method permits to increase the process productivity 3.75-4.50 fold

  3. Correlated Amino Acid and Mineralogical Analyses of Milligram and Submilligram Samples of Carbonaceous Chondrite Lonewolf Nunataks 94101

    Science.gov (United States)

    Burton, S.; Berger, E. L.; Locke, D. R.; Lewis, E. K.

    2018-01-01

    Amino acids, the building blocks of proteins, have been found to be indigenous in the eight carbonaceous chondrite groups. The abundances, structural, enantiomeric and isotopic compositions of amino acids differ significantly among meteorites of different groups and petrologic types. These results suggest parent-body conditions (thermal or aqueous alteration), mineralogy, and the preservation of amino acids are linked. Previously, elucidating specific relationships between amino acids and mineralogy was not possible because the samples analyzed for amino acids were much larger than the scale at which petrologic heterogeneity is observed (sub mm-scale differences corresponding to sub-mg samples); for example, Pizzarello and coworkers measured amino acid abundances and performed X-ray diffraction (XRD) on several samples of the Murchison meteorite, but these analyses were performed on bulk samples that were 500 mg or larger. Advances in the sensitivity of amino acid measurements by liquid chromatography with fluorescence detection/time-of-flight mass spectrometry (LC-FD/TOF-MS), and application of techniques such as high resolution X-ray diffraction (HR-XRD) and scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) for mineralogical characterizations have now enabled coordinated analyses on the scale at which mineral heterogeneity is observed. In this work, we have analyzed samples of the Lonewolf Nunataks (LON) 94101 CM2 carbonaceous chondrite. We are investigating the link(s) between parent body processes, mineralogical context, and amino acid compositions in meteorites on bulk samples (approx. 20mg) and mineral separates (< or = 3mg) from several of spatial locations within our allocated samples. Preliminary results of these analyses are presented here.

  4. Efficacy of commercial baits and new active ingredients against firebrats and silverfish (Zygentoma: Lepismatidae).

    Science.gov (United States)

    Sims, Steven R; Appel, Arthur G

    2012-08-01

    Commercial baits containing boric acid, hydramethynon, and indoxacarb were tested against the firebrat, Thermobia domestica (Packard), and silverfish, Lepisma saccharina L. (both Zygentoma: Lepismatidae), under laboratory conditions. Three boric acid baits were consumed in significantly smaller amounts than untreated control food and did not effectively control either species. Baits containing hydramethylnon and indoxacarb were consumed in greater amounts than boric acid baits, but were relatively ineffective, with LT50 values >9 d. Presence or absence of competitive untreated food did not consistently affect bait efficacy. A ground oat matrix was used to evaluate the potential effectiveness of abamectin, chlorfenapyr, dinotefuran, fipronil, hydramethylnon, metaflumizone, and novaluron baits. The most effective compound was chlorfenapyr. At 0.05 and 0.20% (wt:wt) rates, chlorfenapyr baits produced LT50 values, for both species, ranging from 2 to 4 d. All other compounds had LT50 values >7 d.

  5. Solidification of low-level radioactive wastes in masonry cement

    International Nuclear Information System (INIS)

    Zhou, H.; Colombo, P.

    1987-03-01

    Portland cements are widely used as solidification agents for low-level radioactive wastes. However, it is known that boric acid wastes, as generated at pressurized water reactors (PWR's) are difficult to solidify using ordinary portland cements. Waste containing as little as 5 wt % boric acid inhibits the curing of the cement. For this purpose, the suitability of masonry cement was investigated. Masonry cement, in the US consists of 50 wt % slaked lime (CaOH 2 ) and 50 wt % of portland type I cement. Addition of boric acid in molar concentrations equal to or less than the molar concentration of the alkali in the cement eliminates any inhibiting effects. Accordingly, 15 wt % boric acid can be satisfactorily incorporated into masonry cement. The suitability of masonry cement for the solidification of sodium sulfate wastes produced at boiling water reactors (BWR's) was also investigated. It was observed that although sodium sulfate - masonry cement waste forms containing as much as 40 wt % Na 2 SO 4 can be prepared, waste forms with more than 7 wt % sodium sulfate undergo catastrophic failure when exposed to an aqueous environment. It was determined by x-ray diffraction that in the presence of water, the sulfate reacts with hydrated calcium aluminate to form calcium aluminum sulfate hydrate (ettringite). This reaction involves a volume increase resulting in failure of the waste form. Formulation data were identified to maximize volumetric efficiency for the solidification of boric acid and sodium sulfate wastes. Measurement of some of the waste form properties relevant to evaluating the potential for the release of radionuclides to the environment included leachability, compression strengths and chemical interactions between the waste components and masonry cement. 15 refs., 19 figs., 9 tabs

  6. Gas chromatography/isotope ratio mass spectrometry: analysis of methanol, ethanol and acetic acid by direct injection of aqueous alcoholic and acetic acid samples.

    Science.gov (United States)

    Ai, Guomin; Sun, Tong; Dong, Xiuzhu

    2014-08-15

    Methanol, ethanol, and acetic acid are not easily extracted from aqueous samples and are susceptible to isotope fractionation in gas chromatography/isotope ratio mass spectrometry (GC/IRMS) analysis. Developing a direct dilution GC/IRMS method for aqueous samples, by adjusting the sample concentrations in common solvents to be similar to each other and using a fixed GC split ratio, is very convenient and important because any linearity effects caused by amount-dependent isotope fractionation can be avoided. The suitability of acetonitrile and acetone solvents for the GC/IRMS analysis of pure methanol, ethanol and acetic acid, and commercial liquor and vinegar samples was evaluated using n-hexane and water as control solvents. All the solvents including water were separated from the analyte on a HP-INNOWAX column and were diverted away from the combustion interface. The influence of liquor matrix on the ethanol GC/IRMS analyses was evaluated by adding pure ethanol to liquor samples. Acetonitrile and acetone gave similar δ(13) C values for pure ethanol and pure acetic acid to those obtained in water and n-hexane, and also gave similar δ(13) C values of ethanol in liquor and acetic acid in white vinegar to that obtained in water. For methanol analysis, acetonitrile and refined acetone gave similar δ(13) C values to that obtained in water, but n-hexane was not a suitable solvent. In addition, isotopic fractionation caused by solvent and solute interactions was observed. We recommend using acetonitrile for the GC/IRMS analysis of aqueous alcoholic samples, and acetone for the analysis of aqueous acetic acid samples. This direct dilution method can provide high accurate and precise GC/IRMS analysis of the relative changes in δ(13) C values of methanol, ethanol, and acetic acid. Copyright © 2014 John Wiley & Sons, Ltd.

  7. X-ray fluorescence analysis of Fe, Mn, Cr and V in natural silicate crystals

    International Nuclear Information System (INIS)

    Dias, O.L.; Albuquerque, A.R.P.L.; Isotani, S.

    1983-01-01

    Concentrations of Fe, Mn, Cr and V were determined in samples of beryl, topaze, tourmaline and spodumene by measuring the first order Kα fluorescence lines. The intensity of these lines were calibrated by using beryl as the standard matrix. The matrices were prepared in the form of pressed pellets with 4:1 mixture of beryl and boric acid, where transition metal oxides were added. (Author) [pt

  8. Reverse osmosis and its use at the nuclear power plants. Purification of primary circuit coolant by the means of reverse osmosis

    International Nuclear Information System (INIS)

    Kus, Pavel; Vonkova, Katerina; Kunesova, Katerina; Bartova, Sarka; Skala, Martin; Moucha, Tomáš

    2014-01-01

    This contribution is focused on the use of membrane technologies (e.g. reverse osmosis) for the primary coolant purification at the nuclear power plants. Currently, boric acid present in the primary coolant is preconcentrated at the evaporators, but their operation is very inefficient and expensive. Therefore, reverse osmosis was proposed as one of promising methods possibly replacing evaporators. The aim of the purification process is to achieve boric acid solution of a defined concentration (40 g/l) in the retentate stream in order to recycle it and reuse it in the primary circuit. Additionally, permeate flow should consist solely of pure water. To study the efficiency of several reverse osmosis modulus in the boric acid removal form the water solutions, experimental apparatus was constructed in our laboratory. It consists of the solution reservoir, pump and reverse osmosis modulus. The arrangement of experiments was batch and the retentate flow was refluxed to the feed solution. Several modulus of commercial reverse osmosis membranes were tested. The feed solution contained various concentrations of H 3 BO 3 , KOH, LiOH and NH 3 in order to simulate real primary coolant composition. Based on the experimental results, mathematical model was developed in order to optimize experimental conditions for the best results in primary coolant purification and boric acid preconcentration. (author)

  9. Kinetic and Mechanistic Study of the pH-Dependent Activation (Epoxidation) of Prodrug Treosulfan Including the Reaction Inhibition in a Borate Buffer.

    Science.gov (United States)

    Romański, Michał; Ratajczak, Whitney; Główka, Franciszek

    2017-07-01

    A prodrug treosulfan (T) undergoes a pH-dependent activation to epoxide derivatives. The process seems to involve an intramolecular Williamson reaction (IWR) but clear kinetic evidence is lacking. Moreover, a cis-diol system present in the T structure is expected to promote complexation with boric acid. As a result, the prodrug epoxidation would be inhibited; however, this phenomenon has not been investigated. In this article, the effect of pH on the kinetics of T conversion to its monoepoxide was studied from a mechanistic point of view. Also, the influence of boric acid on the reaction kinetics was examined. The rate constants observed for the activation of T (k obs ) in acetate, phosphate, and carbonate buffers satisfied the equation logk obs  = -7.48 + 0.96 pH. The reaction was inhibited in the excess of boric acid over T, and the k obs decreased with increasing borate buffer concentration. The experimental results were consistent with the inhibition model that included the formation of a tetrahedral, anionic T-boric acid monoester. To conclude, in nonborate buffers, the T activation to (2S,3S)-1,2-epoxybutane-3,4-diol 4-methanesulfonate follows IWR mechanism. A borate buffer changes the reaction kinetics and complicates kinetic analysis. Copyright © 2017 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

  10. Pore water sampling in acid sulfate soils: a new peeper method.

    Science.gov (United States)

    Johnston, Scott G; Burton, Edward D; Keene, Annabelle F; Bush, Richard T; Sullivan, Leigh A; Isaacson, Lloyd

    2009-01-01

    This study describes the design, deployment, and application of a modified equilibration dialysis device (peeper) optimized for sampling pore waters in acid sulfate soils (ASS). The modified design overcomes the limitations of traditional-style peepers, when sampling firm ASS materials over relatively large depth intervals. The new peeper device uses removable, individual cells of 25 mL volume housed in a 1.5 m long rigid, high-density polyethylene rod. The rigid housing structure allows the device to be inserted directly into relatively firm soils without requiring a supporting frame. The use of removable cells eliminates the need for a large glove-box after peeper retrieval, thus simplifying physical handling. Removable cells are easily maintained in an inert atmosphere during sample processing and the 25-mL sample volume is sufficient for undertaking multiple analyses. A field evaluation of equilibration times indicates that 32 to 38 d of deployment was necessary. Overall, the modified method is simple and effective and well suited to acquisition and processing of redox-sensitive pore water profiles>1 m deep in acid sulfate soil or any other firm wetland soils.

  11. Characterization of citrus pectin samples extracted under different conditions: influence of acid type and pH of extraction

    DEFF Research Database (Denmark)

    Kaya, Merve; Sousa, Antonio G.; Crepeau, Marie-Jeanne

    2014-01-01

    on the chemical and macromolecular characteristics of pectin samples. Methods Citrus peel (orange, lemon, lime and grapefruit) from a commercial supplier was used as raw material. Pectin samples were obtained on a bulk plant scale (kilograms; harsh nitric acid, mild nitric acid and harsh oxalic acid extraction......) and on a laboratory scale (grams; mild oxalic acid extraction). Pectin composition (acidic and neutral sugars) and physicochemical properties (molar mass and intrinsic viscosity) were determined. Key Results Oxalic acid extraction allowed the recovery of pectin samples of high molecular weight. Mild oxalic acid......-extracted pectins were rich in long homogalacturonan stretches and contained rhamnogalacturonan I stretches with conserved side chains. Nitric acid-extracted pectins exhibited lower molecular weights and contained rhamnogalacturonan I stretches encompassing few and/or short side chains. Grapefruit pectin was found...

  12. A method for analysing small samples of floral pollen for free and protein-bound amino acids.

    Science.gov (United States)

    Stabler, Daniel; Power, Eileen F; Borland, Anne M; Barnes, Jeremy D; Wright, Geraldine A

    2018-02-01

    Pollen provides floral visitors with essential nutrients including proteins, lipids, vitamins and minerals. As an important nutrient resource for pollinators, including honeybees and bumblebees, pollen quality is of growing interest in assessing available nutrition to foraging bees. To date, quantifying the protein-bound amino acids in pollen has been difficult and methods rely on large amounts of pollen, typically more than 1 g. More usual is to estimate a crude protein value based on the nitrogen content of pollen, however, such methods provide no information on the distribution of essential and non-essential amino acids constituting the proteins.Here, we describe a method of microwave-assisted acid hydrolysis using low amounts of pollen that allows exploration of amino acid composition, quantified using ultra high performance liquid chromatography (UHPLC), and a back calculation to estimate the crude protein content of pollen.Reliable analysis of protein-bound and free amino acids as well as an estimation of crude protein concentration was obtained from pollen samples as low as 1 mg. Greater variation in both protein-bound and free amino acids was found in pollen sample sizes amino acids in smaller sample sizes, we suggest a correction factor to apply to specific sample sizes of pollen in order to estimate total crude protein content.The method described in this paper will allow researchers to explore the composition of amino acids in pollen and will aid research assessing the available nutrition to pollinating animals. This method will be particularly useful in assaying the pollen of wild plants, from which it is difficult to obtain large sample weights.

  13. Fatty Acid Detection in Mars-Analogous Rock Samples with the TMAH Wet Chemistry Experiment on the Sample Analysis at Mars (SAM) Instrument

    Science.gov (United States)

    Williams, A. J.; Eigenbrode, J. L.; Wilhelm, M. B.; Johnson, S. S.; Craft, K.; O'Reilly, S.; Lewis, J. M. T.; Williams, R.; Summons, R. E.; Benison, K. C.; Mahaffy, P. R.

    2017-12-01

    The Curiosity rover is exploring sedimentary rock sequences in Gale Crater for evidence of habitability and searching for organic compounds using the Sample Analysis at Mars (SAM) instrument suite. SAM includes a gas chromatograph mass spectrometer (GC-MS) and pyrolysis ovens. SAM has the ability to perform wet chemistry experiments, one of which uses tetramethylammonium hydroxide (TMAH) thermochemolysis to liberate bound lipids, making them sufficiently volatile for detection by GC-MS. To determine the effectiveness of the SAM-like TMAH experiment on fatty acid methyl ester (FAME) biomarker identification, rock and sediment samples were collected from a variety of Mars analog environments including iron oxides from a modern mineral precipitate and older surface gossan at Iron Mountain, CA, as well as modern acid salt and neutral lake sediments with mixed iron oxides and clays from Western Australia; siliceous sinter from recently inactive and modern near-vent Icelandic hot springs deposits; modern carbonate ooids from The Bahamas, and organic-rich shale from Germany. Samples underwent pyrolysis with TMAH. Fatty acids were analyzed by pyro-GC-MS using a SAM-like heating ramp (35°C/min) as well as a 500°C flash on a Frontier pyrolyzer and Agilent GC-MS instrument. Results reveal that FAMEs were detectable with the TMAH experiment in nearly all samples. Low molecular weight (MW) C6:0-C10:0 FAMEs were present in all samples, medium MW C11:0-C18:2 FAMEs were present in select samples, and high MW (HMW) C20:0-C30:0 FAMEs were present in the shale sample. Many of these samples exhibited an even-over-odd carbon number preference, indicating biological production. These experiments demonstrate that TMAH thermochemolysis with SAM-like pyro-GC-MS is effective in fatty acid analysis from natural Mars-analog samples that vary in mineralogy, age, and microbial community input. HMW FAMEs are not detected in iron-dominated samples, and may not be detectable at low

  14. Reproductive toxicity parameters and biological monitoring in occupationally and environmentally boron-exposed persons in Bandirma, Turkey.

    Science.gov (United States)

    Duydu, Yalçın; Başaran, Nurşen; Üstündağ, Aylin; Aydin, Sevtap; Ündeğer, Ülkü; Ataman, Osman Yavuz; Aydos, Kaan; Düker, Yalçın; Ickstadt, Katja; Waltrup, Britta Schulze; Golka, Klaus; Bolt, Hermann M

    2011-06-01

    Boric acid and sodium borates have been considered as being "toxic to reproduction and development", following results of animal studies with high doses. Experimentally, a NOAEL (no observed adverse effect level) of 17.5 mg B/kg-bw/day has been identified for the (male) reproductive effects of boron in a multigeneration study of rats, and a NOAEL for the developmental effects in rats was identified at 9.6 mg B/kg-bw/day. These values are being taken as the basis of current EU safety assessments. The present study was conducted to investigate the reproductive effects of boron exposure in workers employed in boric acid production plant in Bandirma, Turkey. In order to characterize the external and internal boron exposures, boron was determined in biological samples (blood, urine, semen), in workplace air, in food, and in water sources. Unfavorable effects of boron exposure on the reproductive toxicity indicators (concentration, motility, morphology of the sperm cells and blood levels of follicle-stimulating hormone (FSH), luteinizing hormone (LH), and total testosterone) were not observed. The mean calculated daily boron exposure (DBE) of the highly exposed group was 14.45 ± 6.57 (3.32-35.62) mg/day. These human exposures represent worst-case exposure conditions to boric acid/borates in Turkey. These exposure levels are considerably lower than exposures, which have previously led to reproductive effects in experimental animals. In conclusion, this means that dose levels of boron associated with developmental and reproductive toxic effects in animals are by far not reachable for humans under conditions of normal handling and use.

  15. Acetic Acid Detection Threshold in Synthetic Wine Samples of a Portable Electronic Nose

    Directory of Open Access Journals (Sweden)

    Miguel Macías Macías

    2012-12-01

    Full Text Available Wine quality is related to its intrinsic visual, taste, or aroma characteristics and is reflected in the price paid for that wine. One of the most important wine faults is the excessive concentration of acetic acid which can cause a wine to take on vinegar aromas and reduce its varietal character. Thereby it is very important for the wine industry to have methods, like electronic noses, for real-time monitoring the excessive concentration of acetic acid in wines. However, aroma characterization of alcoholic beverages with sensor array electronic noses is a difficult challenge due to the masking effect of ethanol. In this work, in order to detect the presence of acetic acid in synthetic wine samples (aqueous ethanol solution at 10% v/v we use a detection unit which consists of a commercial electronic nose and a HSS32 auto sampler, in combination with a neural network classifier (MLP. To find the characteristic vector representative of the sample that we want to classify, first we select the sensors, and the section of the sensors response curves, where the probability of detecting the presence of acetic acid will be higher, and then we apply Principal Component Analysis (PCA such that each sensor response curve is represented by the coefficients of its first principal components. Results show that the PEN3 electronic nose is able to detect and discriminate wine samples doped with acetic acid in concentrations equal or greater than 2 g/L.

  16. Rapid determination of the equivalence volume in potentiometric acid-base titrations to a preset pH-I Theory and applications.

    Science.gov (United States)

    Ivaska, A

    1974-06-01

    A new approach to shorten the time needed for an acid-base titration has been made. The method developed is based on the equation for acid-base titrations derived by Ingman and Still. The equation is transformed into such a form that only one titration point is needed to calculate the equivalence volume when the titration is carried out to a preset pH which can be chosen according to the experimental conditions. The method is used for titration of acetic acid, log K(H)(HA) = 4.65, hydroxylammonium ion, log K(H)(HA) approximately 6.2, and boric acid, log K(H)(HA) approximately 9.1, with an error of 0.1-0.5%. In titration of hydrogen ascorbate ion, log K(H)(HA) approximately 11.3, the error obtained was about 0.3-2%.

  17. Co-melting technology in resource recycling of sludge derived from stone processing.

    Science.gov (United States)

    Hu, Shao-Hua; Hu, Shen-Chih; Fu, Yen-Pei

    2012-12-01

    Stone processing sludge (SPS) is a by-product of stone-processing wastewater treatment; it is suitable for use as a raw material for making artificial lightweight aggregates (ALWAs). In this study, boric acid was utilized as a flux to lower sintering temperature. The formation of the viscous glassy phase was observed by DTA curve and changes in XRD patterns. Experiments were conducted to find the optimal combination of sintering temperature, sintering time, and boric acid dosage to produce an ALWA of favorable characteristics in terms of water absorption, bulk density, apparent porosity, compressive strength and weight loss to satisfy Taiwan's regulatory requirements for construction and insulation materials. Optimal results gave a sintering temperature of 850 degrees C for 15 min at a boric acid dosage of 15% by weight of SPS. Results for ALWA favorable characteristics were: 0.21% (water absorption), 0.35% (apparent porosity), 1.67 g/cm3 (bulk density), 66.94 MPa (compressive strength), and less than 0.1% (weight loss).

  18. PWR steam-side chemistry follow program. Final report

    International Nuclear Information System (INIS)

    Economy, G.; Wootten, M.J.

    1982-08-01

    Denting is the diametral reduction of Inconel 600 tubes at the support plates of several nuclear steam generators during operation. This tube deformation was shown to be caused by the expansion forces resulting from formation of voluminous oxide generated by corrosion of the carbon steel support plate. The denting phenomenon and potential methods for its inhibition were investigated in the laboratory using isothermal capsules and heated crevice (heat transfer) testing at temperatures relevant to operating steam generators. Both test methods simulate the tube-support plate geometry and materials. Mathematical models were developed to predict the denting behavior of isothermal capsules. Three additives were investigated as potential denting inhibitors. Soaking with calcium hydroxide or sodium phosphate under heat transfer conditions did not inhibit denting when the environment was recontaminated, in contrast to similar soaks in boric acid which inhibited denting for two to four weeks following recontamination. When the boric acid soak was followed by on-line boric acid treatment, inhibition was maintained

  19. Volume reduction by crystallization of low-level radioactive wastes

    International Nuclear Information System (INIS)

    Grant, D.C.; Murray, A.P.

    1982-01-01

    Low-level radioactive wastes containing boric acid, borax, or sodium sulfate, with radioactive contaminants, are generated during the operation of nuclear power plants. These wastes require disposal, and as such, it is economically and environmentally desirable to reduce their volume. Crystallization was examined in the laboratory as a means of accomplishing this. The crystallizer was operated in both of two modes: evaporative cooling and total evaporation. A 12 wt% boric acid waste feed was concentrated to a 40 to 45 wt% slurry in both modes of operation. Using pure boric acid, a slurry containing over 60 wt% was obtained. An 18.5 wt% borax waste feed was concentrated to 50 wt% in the total evaporative mode and 70 wt% in the evaporatively cooled mode. A 22 wt% sodium sulfate feed was concentrated to a 78 wt% slurry in the total evaporative mode. For all of the feeds, this represents a 4- to 5-fold volume reduction by the crystallizer

  20. Application of self-organising maps towards segmentation of soybean samples by determination of amino acids concentration.

    Science.gov (United States)

    Silva, Lívia Ramazzoti Chanan; Angilelli, Karina Gomes; Cremasco, Hágata; Romagnoli, Érica Signori; Galão, Olívio Fernandes; Borsato, Dionisio; Moraes, Larissa Alexandra Cardoso; Mandarino, José Marcos Gontijo

    2016-09-01

    Soybeans are widely used both for human nutrition and animal feed, since they are an important source of protein, and they also provide components such as phytosterols, isoflavones, and amino acids. In this study, were determined the concentrations of the amino acids lysine, histidine, arginine, asparagine, glutamic acid, glycine, alanine, valine, isoleucine, leucine, tyrosine, phenylalanine present in 14 samples of conventional soybeans and 6 transgenic, cultivated in two cities of the state of Paraná, Londrina and Ponta Grossa. The results were tabulated and presented to a self-organising map for segmentation according planting regions and conventional or transgenic varieties. A network with 7000 training epochs and a 10 × 10 topology was used, and it proved appropriate in the segmentation of the samples using the data analysed. The weight maps provided by the network, showed that all the amino acids were important in targeting the samples, especially isoleucine. Three clusters were formed, one with only Ponta Grossa samples (including transgenic (PGT) and common (PGC)), a second group with Londrina transgenic (LT) samples and the third with Londrina common (LC) samples. Copyright © 2016 Elsevier Masson SAS. All rights reserved.

  1. Evaluation of sampling methods for measuring exposure to volatile inorganic acids in workplace air. Part 2: Sampling capacity and breakthrough tests for sodium carbonate-impregnated filters.

    Science.gov (United States)

    Demange, Martine; Oury, Véronique; Rousset, Davy

    2011-11-01

    In France, the MétroPol 009 method used to measure workplace exposure to inorganic acids, such as HF, HCl, and HNO3, consists of a closed-face cassette fitted with a prefilter to collect particles, and two sodium carbonate-impregnated filters to collect acid vapor. This method was compared with other European methods during the development of a three-part standard (ISO 21438) on the determination of inorganic acids in workplace air by ion chromatography. Results of this work, presented in a companion paper, led to a need to go deeper into the performance of the MétroPol 009 method regarding evaluation of the breakthrough of the acids, both alone and in mixtures, interference from particulate salts, the amount of sodium carbonate required to impregnate the sampling filter, the influence of sampler components, and so on. Results enabled improvements to be made to the sampling device with respect to the required amount of sodium carbonate to sample high HCl or HNO3 concentrations (500 μL of 5% Na2CO3 on each of two impregnated filters). In addition, a PVC-A filter used as a prefilter in a sampling device showed a propensity to retain HNO3 vapor so a PTFE filter was considered more suitable for use as a prefilter. Neither the material of the sampling cassette (polystyrene or polypropylene) nor the sampling flowrate (1 L/min or 2 L/min) influenced the performance of the sampling device, as a recovery of about 100% was achieved in all experiments for HNO3, HCl, and HF, as well as HNO3+HF and HNO3+HCl mixtures, over a wide range of concentrations. However, this work points to the possibility of interference between an acid and salts of other acids. For instance, interference can occur through interaction of HNO3 with chloride salts: the stronger the acid, the greater the interference. Methods based on impregnated filters are reliable for quantitative recovery of inorganic volatile acids in workplace atmosphere but are valuable only in the absence of interferents.

  2. Cementation of wastes with boric acid

    International Nuclear Information System (INIS)

    Tello, Cledola C.O.; Haucz, Maria Judite A.; Alves, Lilian J.L.; Oliveira, Arno H.

    2000-01-01

    In nuclear power plants (PWR) are generated wastes, such as concentrate, which comes from the evaporation of liquid radioactive wastes, and spent resins. Both have boron in their composition. The cementation process is one of the options to solidify these wastes, but the boron has a negative effect on the setting of the cement mixture. In this paper are presented the experiments that are being carried out in order to overcome this problem and also to improve the efficiency of the process. Simulated wastes were cemented using additives (clays, admixtures etc.). In the process and product is being evaluated the effect of the amount, type and addition order of the materials. The mixtures were selected in accordance with their workability and incorporated waste. The solidified products are monolithic without free water with a good mechanical resistance. (author)

  3. Device for borating the primary circuit of a water-cooled nuclear reactor plant

    International Nuclear Information System (INIS)

    Stiefel, M.

    1985-01-01

    The extraction pipes for the boric acid and deionisation container are each connected to a pipe which can be shut off behind the pump. Measures for checking the contents of the container are provided in the extraction pipes and/or in the pipes leading to the containers. Faults can therefore be recognised in good time. The degree of availability is increased and the number of necessary redundant devices is reduced. The extraction pipe of the boric acid container has a rotary displacement pump. (HP) [de

  4. Use of a polystyrene-divinylbenzene-based weakly acidic cation-exchange resin column and propionic acid as an eluent in ion-exclusion/adsorption chromatography of aliphatic carboxylic acids and ethanol in food samples.

    Science.gov (United States)

    Mori, Masanobu; Hironaga, Takahiro; Kajiwara, Hiroe; Nakatani, Nobutake; Kozaki, Daisuke; Itabashi, Hideyuki; Tanaka, Kazuhiko

    2011-01-01

    We developed an ion-exclusion/adsorption chromatography (IEAC) method employing a polystyrene-divinylbenzene-based weakly acidic cation-exchange resin (PS-WCX) column with propionic acid as the eluent for the simultaneous determination of multivalent aliphatic carboxylic acids and ethanol in food samples. The PS-WCX column well resolved mono-, di-, and trivalent carboxylic acids in the acidic eluent. Propionic acid as the eluent gave a higher signal-to-noise ratio, and enabled sensitive conductimetric detection of analyte acids. We found the optimal separation condition to be the combination of a PS-WCX column and 20-mM propionic acid. Practical applicability of the developed method was confirmed by using a short precolumn with a strongly acidic cation-exchange resin in the H(+)-form connected before the separation column; this was to remove cations from food samples by converting them to hydrogen ions. Consequently, common carboxylic acids and ethanol in beer, wine, and soy sauce were successfully separated by the developed method.

  5. The comparison of possibilities at using of different electrolytes in the process of anodizing aluminum

    Directory of Open Access Journals (Sweden)

    M. Gombar

    2014-01-01

    Full Text Available The contribution researches and solves the suitability of utilize of electrolyte, consisting of the oxalic acid, boric acid, sodium chloride and aluminium cations in the process of anodizing aluminium in operating conditions of electrolyte T = 22 °C, t = time of oxidation and the size of at least 210 an applied voltage U = 12 V. The appropriate use of the electrolyte is judged by the thickness of the anodic aluminium oxide layer (AAO formed on the basis of the monitoring and the resulting quality of the sample surface.

  6. X-ray fluorescence analysis of Fe, Mn, Cr and V in natural silicate crystals

    International Nuclear Information System (INIS)

    Dias, O.L.; Albuquerque, A.R.P.L.; Isotani, S.

    1983-04-01

    Concentrations of Fe, Mn, Cr and V were determined in samples of beryl, topaz, tourmaline and spodumene by measuring the first order K sub(α) fluorescence lines. The intensity of these lines were calibrated by using beryl as the standard matrix. The matrices were prepared in the form of pressed pellets with 4:1 mixture of beryl and boric acid, where transition metal oxides were added. (Author) [pt

  7. In vitro assessment of potential intestinal absorption of some phenolic families and carboxylic acids from commercial instant coffee samples.

    Science.gov (United States)

    López-Froilán, R; Ramírez-Moreno, E; Podio, N S; Pérez-Rodríguez, M L; Cámara, M; Baroni, M V; Wunderlin, D A; Sánchez-Mata, M C

    2016-06-15

    Coffee is one of the most consumed beverages in the world, being a source of bioactive compounds as well as flavors. Hydroxycinnamic acids, flavonols, and carboxylic acids have been studied in the samples of instant coffee commercialized in Spain. The studies about contents of food components should be complemented with either in vitro or in vivo bioaccessibility studies to know the amount of food components effectively available for functions in the human body. In this sense, a widely used in vitro model has been applied to assess the potential intestinal absorption of phenolic compounds and organic acids. The contents of hydroxycinnamic acids and flavonols were higher in instant regular coffee samples than in the decaffeinated ones. Bioaccessible phenolic compounds in most analyzed samples account for 20-25% of hydroxycinnamic acids and 17-26% of flavonols. This could mean that a great part of them can remain in the gut, acting as potential in situ antioxidants. Quinic, acetic, pyroglutamic, citric and fumaric acids were identified in commercial instant coffee samples. Succinic acid was found in the coffee blend containing chicory. All carboxylic acids showed a very high bioaccessibility. Particularly, acetic acid and quinic acid were found in higher contents in the samples treated with the in vitro simulation of gastrointestinal processes, compared to the original ones, which can be explained by their cleavage from chlorogenic acid during digestion. This is considered as a positive effect, since quinic acid is considered as an antioxidant inducer.

  8. HPLC/DAD determination of rosmarinic acid in Salvia officinalis: sample preparation optimization by factorial design

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Karina B. de [Universidade Federal do Parana (UFPR), Curitiba, PR (Brazil). Dept. de Farmacia; Oliveira, Bras H. de, E-mail: bho@ufpr.br [Universidade Federal do Parana (UFPR), Curitiba, PR (Brazil). Dept. de Quimica

    2013-01-15

    Sage (Salvia officinalis) contains high amounts of the biologically active rosmarinic acid (RA) and other polyphenolic compounds. RA is easily oxidized, and may undergo degradation during sample preparation for analysis. The objective of this work was to develop and validate an analytical procedure for determination of RA in sage, using factorial design of experiments for optimizing sample preparation. The statistically significant variables for improving RA extraction yield were determined initially and then used in the optimization step, using central composite design (CCD). The analytical method was then fully validated, and used for the analysis of commercial samples of sage. The optimized procedure involved extraction with aqueous methanol (40%) containing an antioxidant mixture (ascorbic acid and ethylenediaminetetraacetic acid (EDTA)), with sonication at 45 deg C for 20 min. The samples were then injected in a system containing a C{sub 18} column, using methanol (A) and 0.1% phosphoric acid in water (B) in step gradient mode (45A:55B, 0-5 min; 80A:20B, 5-10 min) with flow rate of 1.0 mL min-1 and detection at 330 nm. Using this conditions, RA concentrations were 50% higher when compared to extractions without antioxidants (98.94 {+-} 1.07% recovery). Auto-oxidation of RA during sample extraction was prevented by the use of antioxidants resulting in more reliable analytical results. The method was then used for the analysis of commercial samples of sage. (author)

  9. HPLC/DAD determination of rosmarinic acid in Salvia officinalis: sample preparation optimization by factorial design

    International Nuclear Information System (INIS)

    Oliveira, Karina B. de; Oliveira, Bras H. de

    2013-01-01

    Sage (Salvia officinalis) contains high amounts of the biologically active rosmarinic acid (RA) and other polyphenolic compounds. RA is easily oxidized, and may undergo degradation during sample preparation for analysis. The objective of this work was to develop and validate an analytical procedure for determination of RA in sage, using factorial design of experiments for optimizing sample preparation. The statistically significant variables for improving RA extraction yield were determined initially and then used in the optimization step, using central composite design (CCD). The analytical method was then fully validated, and used for the analysis of commercial samples of sage. The optimized procedure involved extraction with aqueous methanol (40%) containing an antioxidant mixture (ascorbic acid and ethylenediaminetetraacetic acid (EDTA)), with sonication at 45 deg C for 20 min. The samples were then injected in a system containing a C 18 column, using methanol (A) and 0.1% phosphoric acid in water (B) in step gradient mode (45A:55B, 0-5 min; 80A:20B, 5-10 min) with flow rate of 1.0 mL min−1 and detection at 330 nm. Using this conditions, RA concentrations were 50% higher when compared to extractions without antioxidants (98.94 ± 1.07% recovery). Auto-oxidation of RA during sample extraction was prevented by the use of antioxidants resulting in more reliable analytical results. The method was then used for the analysis of commercial samples of sage. (author)

  10. Direct methylation procedure for converting fatty amides to fatty acid methyl esters in feed and digesta samples.

    Science.gov (United States)

    Jenkins, T C; Thies, E J; Mosley, E E

    2001-05-01

    Two direct methylation procedures often used for the analysis of total fatty acids in biological samples were evaluated for their application to samples containing fatty amides. Methylation of 5 mg of oleamide (cis-9-octadecenamide) in a one-step (methanolic HCl for 2 h at 70 degrees C) or a two-step (sodium methoxide for 10 min at 50 degrees C followed by methanolic HCl for 10 min at 80 degrees C) procedure gave 59 and 16% conversions of oleamide to oleic acid, respectively. Oleic acid recovery from oleamide was increased to 100% when the incubation in methanolic HCl was lengthened to 16 h and increased to 103% when the incubation in methoxide was modified to 24 h at 100 degrees C. However, conversion of oleamide to oleic acid in an animal feed sample was incomplete for the modified (24 h) two-step procedure but complete for the modified (16 h) one-step procedure. Unsaturated fatty amides in feed and digesta samples can be converted to fatty acid methyl esters by incubation in methanolic HCl if the time of exposure to the acid catalyst is extended from 2 to 16 h.

  11. Absorção e redistribuição de boro em coqueiro-anão-verde Boron absorption and redistribution in green dwarf coconut tree

    Directory of Open Access Journals (Sweden)

    Leandro Glaydson da Rocha Pinho

    2008-12-01

    Full Text Available O objetivo deste trabalho foi verificar se ocorre redistribuição de boro em coqueiros (Cocos nucifera, quando a aplicação de ácido bórico é realizada na axila foliar ou no solo. Foram empregados os seguintes tratamentos com ácido bórico: 30 g aplicados sobre a axila da folha número 10; 60 g aplicados ao solo; e controle, sem aplicação. Foram realizadas duas aplicações de B, com um intervalo de cinco meses entre elas. A unidade experimental consistiu de duas plantas, com seis repetições, em delineamento inteiramente casualizado. Foram determinados os teores de boro nas folhas 2, 6, 10, 14 e 18, aos dois e quatro meses após a primeira aplicação de ácido bórico, e aos dois e cinco meses após a segunda aplicação. O boro se redistribuiu pela planta de coqueiro, independentemente da forma de aplicação. A elevação do teor de boro nas folhas persistiu por mais tempo, quando a aplicação de ácido bórico foi feita ao solo. As doses de ácido bórico aplicadas não causaram fitotoxidade, mesmo quando a aplicaçãofoi repetida após um curto período.The aim of this work was to verify if boron redistribution occurs among the coconut palm (Cocos nucifera fronds, when boric acid is applied on frond axils or on soil. The treatments with boric acid were: 30 g applied on the axil of frond number 10; 60 g applied to the soil; and a control without boric acid application. The B applications were repeated after five-month interval. The experimental unit consisted of two plants, with six replicates, in a randomized complete block design. Boron contents were determined in fronds number 2, 6, 10, 14 and 18, two and four months after the first boric acid application, and two and five months after the second application. Boron was redistributed in coconut plants, regardless of the application form. Increases in boron concentration in fronds persisted longer when boric acid was applied to the soil. The applied doses of boric acid hadno

  12. Preliminary observations on the metal content in some milk samples from an acid geoenvironment

    Directory of Open Access Journals (Sweden)

    Alhonen, P.

    1997-12-01

    Full Text Available The metal content of some milk samples was analyzed from areas of acid sulphate soils along the course of the river Kyrönjoki in western Finland. Comparative analyses were made with samples from the Artjärvi-Porlammi area. The variations of analyzed metals AI, Ba, Ca, Cr, Cu, Fe, K, Mg, Mo, Na, Sr and Zn are not great in both areas except that of Al, which is clearly associated with the acid environment in the Kyrönjoki valley. The portions of these elements in milk are relatively high as compared with data from literature. It is obvious that they show environmental contamination. Under acid circumstances the metals in milk may create serious geomedical problems.

  13. A basic study for the boron thermal regeneration system using anion exchange resins

    International Nuclear Information System (INIS)

    Frantiesek, P.; Kotaka, Masahiro; Okamoto, Makoto; Kakihana, Hidetake.

    1979-01-01

    For the boron thermal regeneration system (BTRS), the basic characteristics of commercial anion exchange resin have been investigated on the swelling characteristics, absorption, desorption and temperature coefficient of exchange capacity for boric acid. The equilibrium capacity increases as decrease of temperature and depends strongly on the degrees of cross linking having a maximum point at about 7% of DVB. The temperature coefficient of equilibrium capacity of boric acid is also a function of the concentration of external solution and of the cross linking having a maximum point around 7% of DVB. (author)

  14. Spectroscopic quantification of 5-hydroxymethylcytosine in genomic DNA using boric acid-functionalized nano-microsphere fluorescent probes.

    Science.gov (United States)

    Chen, Hua-Yan; Wei, Jing-Ru; Pan, Jiong-Xiu; Zhang, Wei; Dang, Fu-Quan; Zhang, Zhi-Qi; Zhang, Jing

    2017-05-15

    5-hydroxymethylcytosine (5hmC) is the sixth base of DNA. It is involved in active DNA demethylation and can be a marker of diseases such as cancer. In this study, we developed a simple and sensitive 2-(4-boronophenyl)quinoline-4-carboxylic acid modified poly (glycidyl methacrylate (PBAQA-PGMA) fluorescent probe to detect the 5hmC content of genomic DNA based on T4 β-glucosyltransferase-catalyzed glucosylation of 5hmC. The fluorescence-enhanced intensity recorded from the DNA sample was proportional to its 5-hydroxymethylcytosine content and could be quantified by fluorescence spectrophotometry. The developed probe showed good detection sensitivity and selectivity and a good linear relationship between the fluorescence intensity and the concentration of 5 hmC within a 0-100nM range. Compared with other fluorescence detection methods, this method not only could determine trace amounts of 5 hmC from genomic DNA but also could eliminate the interference of fluorescent dyes and the need for purification. It also could avoid multiple labeling. Because the PBAQA-PGMA probe could enrich the content of glycosyl-5-hydroxymethyl-2-deoxycytidine from a complex ground substance, it will broaden the linear detection range and improve sensitivity. The limit of detection was calculated to be 0.167nM after enrichment. Furthermore, the method was successfully used to detect 5-hydroxymethylcytosine from mouse tissues. Copyright © 2016 Elsevier B.V. All rights reserved.

  15. Employing natural reagents from turmeric and lime for acetic acid determination in vinegar sample.

    Science.gov (United States)

    Supharoek, Sam-Ang; Ponhong, Kraingkrai; Siriangkhawut, Watsaka; Grudpan, Kate

    2018-04-01

    A simple, rapid and environmentally friendly sequential injection analysis system employing natural extract reagents was developed for the determination of acetic acid following an acid-base reaction in the presence of an indicator. Powdered lime and turmeric were utilized as the natural base and indicator, respectively. Mixing lime and turmeric produced an orange to reddish-brown color solution which absorbed the maximum wavelength at 455 nm, with absorbance decreasing with increasing acetic acid concentration. Influential parameters including lime and turmeric concentrations, reagent and sample aspirated volumes, mixing coil length and dispensing flow rate were investigated and optimized. A standard calibration graph was plotted for 0-5.0 mmol/L acetic acid with r 2  = 0.9925. Relative standard deviations (RSD) at 2.0 and 4.0 mmol/L acetic acid were less than 3% (n = 7), with limit of detection (LOD) and limit of quantification (LOQ) at 0.12 and 0.24 mmol/L, respectively. The method was successfully applied to assay acetic acid concentration in cooking vinegar samples. Results achieved were not significantly different from those obtained following a batchwise standard AOAC titration method. Copyright © 2017. Published by Elsevier B.V.

  16. Employing natural reagents from turmeric and lime for acetic acid determination in vinegar sample

    Directory of Open Access Journals (Sweden)

    Sam-ang Supharoek

    2018-04-01

    Full Text Available A simple, rapid and environmentally friendly sequential injection analysis system employing natural extract reagents was developed for the determination of acetic acid following an acid–base reaction in the presence of an indicator. Powdered lime and turmeric were utilized as the natural base and indicator, respectively. Mixing lime and turmeric produced an orange to reddish-brown color solution which absorbed the maximum wavelength at 455 nm, with absorbance decreasing with increasing acetic acid concentration. Influential parameters including lime and turmeric concentrations, reagent and sample aspirated volumes, mixing coil length and dispensing flow rate were investigated and optimized. A standard calibration graph was plotted for 0–5.0 mmol/L acetic acid with r2 = 0.9925. Relative standard deviations (RSD at 2.0 and 4.0 mmol/L acetic acid were less than 3% (n = 7, with limit of detection (LOD and limit of quantification (LOQ at 0.12 and 0.24 mmol/L, respectively. The method was successfully applied to assay acetic acid concentration in cooking vinegar samples. Results achieved were not significantly different from those obtained following a batchwise standard AOAC titration method. Keywords: Acetic acid assay, Natural reagent, Turmeric, Lime, Sequential injection analysis

  17. Fast derivatization of fatty acids in different meat samples for gas chromatography analysis.

    Science.gov (United States)

    Figueiredo, Ingrid Lima; Claus, Thiago; Oliveira Santos Júnior, Oscar; Almeida, Vitor Cinque; Magon, Thiago; Visentainer, Jesuí Vergilio

    2016-07-22

    In order to analyze the composition of fatty acids employing gas chromatography as the separation method, a derivatization of lipids using esterification and transesterification reactions is needed. The methodologies currently available are time consuming and use large amounts of sample and reagents. Thus, this work proposes a new procedure to carry out the derivatization of fatty acids without the need for prior extraction of lipids. The use of small amounts of sample (100mg) allows the analysis to be performed in specific parts of animals, in most cases without having them slaughtered. Another benefit is the use of small amounts of reagents (only 2mL of NaOH/Methanol and H2SO4/Methanol). The use of an experimental design procedure (Design Expert software) allows the optimization of the alkaline and acid reaction times. The procedure was validated for five minutes in both steps. The method was validated for bovine fat, beef, chicken, pork, fish and shrimp meats. The results for the merit figures of accuracy (from 101.07% to 109.18%), precision (RSDintra-day (from 0.65 to 3.93%), RSDinter-day (from 1.57 to 5.22%)), linearity (R(2)=0.9864) and robustness confirmed that the new method is satisfactory within the linear range of 2-30% of lipids in the sample. Besides the benefits of minimizing the amount of samples and reagents, the procedure enables gas chromatography sample preparation in a very short time compared with traditional procedures. Copyright © 2016 Elsevier B.V. All rights reserved.

  18. The determination of magnesium in simulated PWR coolant by graphite furnace atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Gatford, C.; Torrance, K.

    1988-06-01

    The determination of magnesium in simulated PWR coolant has been investigated by graphite furnace atomic absorption spectrometry with atomization from a L'vov platform. The presence of boric acid in the coolant suppresses the magnesium absorption to such an extent that removal of the boron is necessary and three variations of a methyl borate volatilization technique for the in situ removal of boron from the sample platform were investigated. This work has shown that dilution of the sample with an equal volume of acidified methanol and volatilization of the methyl borate was adequate for the determination of magnesium in coolant samples containing up to 2000 mg 1 -1 of boron. In simulated coolant samples containing 25 and 4 μg 1 -1 of magnesium, positive biases of about 2 and 0.5 μg 1 -1 were measured and these errors were considered to be due to contamination. The limit of detection in the presence of 100 and 2000 mg 1 -1 boron were 0.14 and 0.93 μg 1 -1 respectively. These performance characteristics suggest the method is completely acceptable for monitoring the chemical purity of PWR coolant and associated waters containing boric acid. If, however, more precise analyses were to be required for research purposes then any significant improvement in the above figures would require increased purity of reagents, clean-room conditions to reduce contamination and a more versatile atomic absorption spectrophotometer. (author)

  19. Impact of urine preservation methods and duration of storage on measured levels of environmental contaminants.

    Science.gov (United States)

    Hoppin, Jane A; Ulmer, Ross; Calafat, Antonia M; Barr, Dana B; Baker, Susan V; Meltzer, Helle M; Rønningen, Kjersti S

    2006-01-01

    Collection of urine samples in human studies involves choices regarding shipping, sample preservation, and storage that may ultimately influence future analysis. As more studies collect and archive urine samples to evaluate environmental exposures in the future, we were interested in assessing the impact of urine preservative, storage temperature, and time since collection on nonpersistent contaminants in urine samples. In spiked urine samples stored in three types of urine vacutainers (no preservative, boric acid, and chlorhexidine), we measured five groups of contaminants to assess the levels of these analytes at five time points (0, 24, 48, and 72 h, and 1 week) and at two temperatures (room temperature and 4 degrees C). The target chemicals were bisphenol A (BPA), metabolites of organophosphate (OP), carbamate, and pyrethroid insecticides, chlorinated phenols, and phthalate monoesters, and were measured using five different mass spectrometry-based methods. Three samples were analyzed at each time point, with the exception of BPA. Repeated measures analysis of variance was used to evaluate effects of storage time, temperature, and preservative. Stability was summarized with percent change in mean concentration from time 0. In general, most analytes were stable under all conditions with changes in mean concentration over time, temperature, and preservative being generally less than 20%, with the exception of the OP metabolites in the presence of boric acid. The effect of storage temperature was less important than time since collection. The precision of the laboratory measurements was high allowing us to observe small differences, which may not be important when categorizing individuals into broader exposure groups.

  20. Aluminium, extractable from soil samples by the acid ammonium acetate soil-testing method

    Directory of Open Access Journals (Sweden)

    Osmo Mäkitie

    1968-05-01

    Full Text Available The extractant, 0.5 M acetic acid –0.5 M ammonium acetate at pH 4.65, which is used in soil-testing, extracts relatively high amounts of aluminium from acid soils. The mean values of acetate-extractable aluminium at pH 4.65, 1.75 meq Al/100 g of soil, and of exchangeable aluminium (M KCI extraction, 0.41 meq Al were obtained from a material of 30 samples of acid soils (Table 2. Several other acetic acid ammonium acetate extractants, from M acetic acid to M ammonium acetate solution were also used for studying the extractability of soil aluminium. The soil-testing extractant can be used for the estimation of the soluble amounts of aluminium in acid soils, however, further studies are needed for a better interpretation of the ammonium acetate extractable (at pH 4.65 aluminium in our soils.

  1. Method of preventing criticality of fresh fuel assembly in storage facility

    International Nuclear Information System (INIS)

    Kawamura, Makoto.

    1990-01-01

    With an aim of improving the operation efficiency of a reactor, extention of the operation cycle by increasing U 235 enrichment degree of fuel uranium is planned. However, along with the increase of the enrichment degree of the fuel uranium, there occurs a problem of criticality upon fuel handling. Then, in the present invention, boric acid incorporating B-10 of great neutron absorption effect are packed with water soluble polymeric materials which are further packed with a fuel packing sheet, or the water soluble polymeric materials incorporating boric acids are packed with fuel packing sheets which are disposed to a fresh fuel assembly and stored in a store house as they are. The fuel packing sheet is a perforated sheet having a plurality of water intruding pores. Then, if water should intrude to the store house accidentally, the water soluble polymeric materials are dissolved, so that the intruded water is converted into aqueous boric acid easily and absorbs neutrons effectively to thereby attain the prevention of criticality. (T.M.)

  2. Implementation of antimicrobial peptides for sample preparation prior to nucleic acid amplification in point-of-care settings.

    Science.gov (United States)

    Krõlov, Katrin; Uusna, Julia; Grellier, Tiia; Andresen, Liis; Jevtuševskaja, Jekaterina; Tulp, Indrek; Langel, Ülo

    2017-12-01

    A variety of sample preparation techniques are used prior to nucleic acid amplification. However, their efficiency is not always sufficient and nucleic acid purification remains the preferred method for template preparation. Purification is difficult and costly to apply in point-of-care (POC) settings and there is a strong need for more robust, rapid, and efficient biological sample preparation techniques in molecular diagnostics. Here, the authors applied antimicrobial peptides (AMPs) for urine sample preparation prior to isothermal loop-mediated amplification (LAMP). AMPs bind to many microorganisms such as bacteria, fungi, protozoa and viruses causing disruption of their membrane integrity and facilitate nucleic acid release. The authors show that incubation of E. coli with antimicrobial peptide cecropin P1 for 5 min had a significant effect on the availability of template DNA compared with untreated or even heat treated samples resulting in up to six times increase of the amplification efficiency. These results show that AMPs treatment is a very efficient sample preparation technique that is suitable for application prior to nucleic acid amplification directly within biological samples. Furthermore, the entire process of AMPs treatment was performed at room temperature for 5 min thereby making it a good candidate for use in POC applications.

  3. Determination of 5-caffeoylquinic acid (5-CQA as one of the major classes of chlorogenic acid in commercial tea and coffee samples

    Directory of Open Access Journals (Sweden)

    Grujić-Letić Nevena

    2015-01-01

    Full Text Available Background/Aim. Tea and coffee are one of the most widely consumed beverages in the world due to their beneficial health effects which are largely associated with their phenolic compounds composition, including chlorogenic acid. The main aim of this study was to determine 5-caffeoylquinic acid (5-CQA, as one of the major classes of chlorogenic acid, in various commercial tea and coffee samples present at the Serbian market. Methods. A high-performance liquid chromatography (HPLC method for determination of 5-CQA in plant extracts was applied to determine the content of this active compound in commercial tea and coffee samples. Mobile phase was aqueous 1.5% acetic acid - methanol (80:20, v/v with the flow rate of 0.8 mL/min. Run time was 15 min and column temperature 25°C. The detection was performed at 240 nm. Results. The HPLC method was modified and revalidated. The 5-CQA content varied depending on the type of tea (white, green, black tea and mate and the processing technology. Green tea had the highest 5-CQA content (16 mg/100 mL among the analyzed tea samples. The content of 5-CQA in coffee samples ranged 0-36.20 mg/g of coffee and 0-46.98 mg/100 mL of beverage, showing that the content varied depending on the type of coffee, coffee processing technology and the formulation. Conclusion. The modified and revalidated HPLC method showed a good accuracy, repeatability, selectivity and robustness. The highest amount of 5-CQA was determined in green tea in comparison to white, black and mate tea because the increased oxidation level decreases the amount of 5-CQA. The obtained results for commercial coffee samples indicated that the formulation was the most important factor determining the amount of 5-CQA. It can be concluded that plant material selection, processing conditions and formulation have great influence on the amount of chlorogenic acid (5-CQA in the final tea and coffee products. [Projekat Ministarstva nauke Republike Srbije, br. OI

  4. Determination of 5-caffeoylquinic acid (5-CQA) as one of the major classes of chlorogenic acid in commercial tea and coffee samples.

    Science.gov (United States)

    Nevena, Grujić-Letić; Branislava, Rakić; Emilia, Sefer; Dusica, Rakić; Ivan, Nedeljković; Nebojsa, Kladar; Biljana, Božin

    2015-11-01

    Tea and coffee are one of the most widely consumed beverages in the world due to their beneficial health effects which are largely associated with their phenolic compounds composition, including chlorogenic acid. The main aim of this study was to determine 5-caffeoylquinic acid (5-CQA), as one of the major classes of chlorogenic acid, in various commercial tea and coffee samples present at the Serbian market. A high-performance liquid chromatography (HPLC) method for determination of 5-CQA in plant extracts was applied to determine the content of this active compound in commercial tea and coffee samples. Mobile phase was aqueous 1.5% acetic acid-methanol (80:20, v/v) with the flow rate of 0.8 mL/min. Run time was 15 min and column temperature 25°C. The detection was performed at 240 nm. The HPLC method was modified and revalidated. The 5-CQA content varied depending on the type of tea (white, green, black tea and mate) and the processing technology. Green tea had the highest 5-CQA content (16 mg/100 mL) among the analyzed tea samples. The content of 5-CQA in coffee samples ranged 0-36.20 mg/g of coffee and 0-46.98 mg/100 mL of beverage, showing that the content varied depending on the type of coffee, coffee processing technology and the formulation. The modified and revalidated HPLC method showed a good accuracy, repeatability, selectivity and robustness. The highest amount of 5-CQA was determined in green tea in comparison to white, black and mate tea because the increased oxidation level decreases the amount of 5-CQA. The obtained results for commercial coffee samples indicated that the formulation was the most important factor determining the amount of 5-CQA. It can be concluded that plant material selection, processing conditions and formulation have great influence on the amount of chlorogenic acid (5-CQA) in the final tea and coffee products.

  5. Osteoinduction on acid and heat treated porous Ti metal samples in canine muscle.

    Directory of Open Access Journals (Sweden)

    Toshiyuki Kawai

    Full Text Available Samples of porous Ti metal were subjected to different acid and heat treatments. Ectopic bone formation on specimens embedded in dog muscle was compared with the surface characteristics of the specimen. Treatment of the specimens by H2SO4/HCl and heating at 600 °C produced micrometer-scale roughness with surface layers composed of rutile phase of titanium dioxide. The acid- and heat-treated specimens induced ectopic bone formation within 6 months of implantation. A specimen treated using NaOH followed by HCl acid and then heat treatment produced nanometer-scale surface roughness with a surface layer composed of both rutile and anatase phases of titanium dioxide. These specimens also induced bone formation after 6 months of implantation. Both these specimens featured positive surface charge and good apatite-forming abilities in a simulated body fluid. The amount of the bone induced in the porous structure increased with apatite-forming ability and higher positive surface charge. Untreated porous Ti metal samples showed no bone formation even after 12 months. Specimens that were only heat treated featured a smooth surface composed of rutile. A mixed acid treatment produced specimens with micrometer-scale rough surfaces composed of titanium hydride. Both of them also showed no bone formation after 12 months. The specimens that showed no bone formation also featured almost zero surface charge and no apatite-forming ability. These results indicate that osteoinduction of these porous Ti metal samples is directly related to positive surface charge that facilitates formation of apatite on the metal surfaces in vitro.

  6. Analysis of non-esterified fatty acids in human samples by solid-phase-extraction and gas chromatography/mass spectrometry.

    Science.gov (United States)

    Kopf, Thomas; Schmitz, Gerd

    2013-11-01

    The determination of the fatty acid (FA) profile of lipid classes is essential for lipidomic analysis. We recently developed a GC/MS-method for the analysis of the FA profile of total FAs, i.e. the totality of bound and unbound FAs, in any given biological sample (TOFAs). Here, we present a method for the analysis of non-esterified fatty acids (NEFAs) in biological samples, i.e. the fraction that is present as extractable free fatty acids. Lipid extraction is performed according to Dole using 80/20 2-propanol/n-hexane (v/v), with 0.1% H2SO4. The fatty acid-species composition of this NEFA-fraction is determined as FAME after derivatization with our GC/MS-method on a BPX column (Shimadzu). Validation of the NEFA-method presented was performed in human plasma samples. The validated method has been used with human plasma, cells and tissues, as well as mammalian body fluids and tissue samples. The newly developed solid-phase-extraction (SPE)-GC-MS method allows the rapid separation of the NEFA-fraction from a neutral lipid extract of plasma samples. As a major advantage compared to G-FID-methods, GC-MS allows the use of stable isotope labeled fatty acid precursors to monitor fatty acid metabolism. Copyright © 2013 Elsevier B.V. All rights reserved.

  7. Inhibition and Kinetic Studies of Tortoise (Kinixys erosa) Liver arginase

    African Journals Online (AJOL)

    The effect of amino acid on tortoise liver arginase showed that L-lysine, L-valine, L-serine, L-aspartic acid and L aspartic acid had significant inhibitory effect on the enzyme but proline and glutamic acid showed slight inhibition. Ethylenediaminetetraacetic acid (EDTA), citrate, ascorbic acid, boric acid and sodium borate ...

  8. Determination of ethanol in acetic acid-containing samples by a biosensor based on immobilized Gluconobacter cells

    Directory of Open Access Journals (Sweden)

    VALENTINA A. KRATASYUK

    2012-11-01

    Full Text Available Reshetilov AN, Kitova AE, Arkhipova AV, Kratasyuk VA, Rai MK. 2012. Determination of ethanol in acetic acid containing samples by a biosensor based on immobilized Gluconobacter cells. Nusantara Bioscience 4: 97-100. A biosensor based on Gluconobacter oxydans VKM B-1280 bacteria was used for detection of ethanol in the presence of acetic acid. It was assumed that this assay could be useful for controlling acetic acid production from ethanol and determining the final stage of the fermentation process. Measurements were made using a Clark electrode-based amperometric biosensor. The effect of pH of the medium on the sensor signal and the analytical parameters of the sensor (detection range, sensitivity were investigated. The residual content of ethanol in acetic acid samples was analyzed. The results of the study are important for monitoring the acetic acid production process, as they represent a method of tracking its stages

  9. Determination of acrolein, ethanol, volatile acidity, and copper in different samples of sugarcane spirits

    Directory of Open Access Journals (Sweden)

    José Masson

    2012-09-01

    Full Text Available Seventy-one samples of sugarcane spirits from small and average size stills produced in the northern and southern Minas Gerais (Brazil were analyzed for acrolein using HPLC (High Performance Liquid Chromatography. Ethanol and copper concentrations and volatile acidity were also determined according to methods established by the Ministry of Agriculture, Livestock and Supply (MAPA. A total of 9.85% of the samples tested showed levels of acrolein above the legal limits, while the copper concentrations of 21.00% of the samples and the volatile acidity of 8.85% of the samples were higher than the limits established by the Brazilian legislation. The concentration of acrolein varied from 0 to 21.97 mg.100 mL-1 of ethanol. However, no significant difference at 5% of significance was observed between the samples produced in the northern and southern Minas Gerais. The method used for determination of acrolein in sugarcane spirits involved the formation of a derivative with 2,4-dinitrophenylhydrazine (2,4-DNPH and subsequent analysis by HPLC.

  10. Membrane systems and their use in nuclear power plants. Treatment of primary coolant

    Energy Technology Data Exchange (ETDEWEB)

    Kus, Pavel; Bartova, Sarka; Skala, Martin; Vonkova, Katerina [Research Centre Rez, Husinec-Rez (Czech Republic). Technological Circuits Innovation Dept.; Zach, Vaclav; Kopa, Roman [CEZ a.s., Temelin (Czech Republic). Nuclear Power Plant Temelin

    2016-03-15

    In nuclear power plants, drained primary coolant containing boric acid is currently treated in the system of evaporators and by ion exchangers. Replacement of the system of evaporators by membrane system (MS) will result in lower operating cost mainly due to lower operation temperature. In membrane systems the feed primary coolant is separated into two output streams: retentate and permeate. Retentate stream consists of the concentrated boric acid solution together with other components, while permeate stream consists of purified water. Results are presented achieved by testing a pilot-plant unit of reverse osmosis in nuclear power plant (NPP) Temelin.

  11. Neutronic-thermohydraulic oscillatory instability in modern PWRs due to high concentrations of boron in the water

    International Nuclear Information System (INIS)

    Novelli, A.

    1985-01-01

    Conspicuous amounts of boric acid are normally dissolved into the moderator of a modern PWR, especially in BOL operative conditions. If the concentration of such a neutronic poison attains certain limits, the nuclear temperature coefficient of the moderator, which is highly negative in the absence of boron, may turn about and reach positive values, due to the strong thermal expansion of the water. A dynamical model of a PWR system is presented, facilitating a quick stability analysis related to the co-ordination of boric acid solution in the water and control-rod insertion in the core. (author)

  12. Characterization of citrus pectin samples extracted under different conditions: influence of acid type and pH of extraction

    Science.gov (United States)

    Kaya, Merve; Sousa, António G.; Crépeau, Marie-Jeanne; Sørensen, Susanne O.; Ralet, Marie-Christine

    2014-01-01

    Background and Aims Pectin is a complex macromolecule, the fine structure of which is influenced by many factors. It is used as a gelling, thickening and emulsifying agent in a wide range of applications, from food to pharmaceutical products. Current industrial pectin extraction processes are based on fruit peel, a waste product from the juicing industry, in which thousands of tons of citrus are processed worldwide every year. This study examines how pectin components vary in relation to the plant source (orange, lemon, lime, grapefruit) and considers the influence of extraction conditions on the chemical and macromolecular characteristics of pectin samples. Methods Citrus peel (orange, lemon, lime and grapefruit) from a commercial supplier was used as raw material. Pectin samples were obtained on a bulk plant scale (kilograms; harsh nitric acid, mild nitric acid and harsh oxalic acid extraction) and on a laboratory scale (grams; mild oxalic acid extraction). Pectin composition (acidic and neutral sugars) and physicochemical properties (molar mass and intrinsic viscosity) were determined. Key Results Oxalic acid extraction allowed the recovery of pectin samples of high molecular weight. Mild oxalic acid-extracted pectins were rich in long homogalacturonan stretches and contained rhamnogalacturonan I stretches with conserved side chains. Nitric acid-extracted pectins exhibited lower molecular weights and contained rhamnogalacturonan I stretches encompassing few and/or short side chains. Grapefruit pectin was found to have short side chains compared with orange, lime and lemon. Orange and grapefruit pectin samples were both particularly rich in rhamnogalacturonan I backbones. Conclusions Structural, and hence macromolecular, variations within the different citrus pectin samples were mainly related to their rhamnogalacturonan I contents and integrity, and, to a lesser extent, to the length of their homogalacturonan domains. PMID:25081519

  13. Sequential injection titration method using second-order signals: determination of acidity in plant oils and biodiesel samples.

    Science.gov (United States)

    del Río, Vanessa; Larrechi, M Soledad; Callao, M Pilar

    2010-06-15

    A new concept of flow titration is proposed and demonstrated for the determination of total acidity in plant oils and biodiesel. We use sequential injection analysis (SIA) with a diode array spectrophotometric detector linked to chemometric tools such as multivariate curve resolution-alternating least squares (MCR-ALS). This system is based on the evolution of the basic specie of an acid-base indicator, alizarine, when it comes into contact with a sample that contains free fatty acids. The gradual pH change in the reactor coil due to diffusion and reaction phenomenona allows the sequential appearance of both species of the indicator in the detector coil, recording a data matrix for each sample. The SIA-MCR-ALS method helps to reduce the amounts of sample, the reagents and the time consumed. Each determination consumes 0.413ml of sample, 0.250ml of indicator and 3ml of carrier (ethanol) and generates 3.333ml of waste. The frequency of the analysis is high (12 samples h(-1) including all steps, i.e., cleaning, preparing and analysing). The utilized reagents are of common use in the laboratory and it is not necessary to use the reagents of perfect known concentration. The method was applied to determine acidity in plant oil and biodiesel samples. Results obtained by the proposed method compare well with those obtained by the official European Community method that is time consuming and uses large amounts of organic solvents.

  14. Searching for Amino Acids in Meteorites and Comet Samples

    Science.gov (United States)

    Cook, Jamie Elsila

    2010-01-01

    Chemistry plays an important role in the interdisciplinary field of astrobiology, which strives to understand the origin, distribution, and evolution of life throughout the universe. Chemical techniques are used to search for and characterize the basic ingredients for life, from the elements through simple molecules and up to the more complex compounds that may serve as the ingredients for life. The Astrobiology Analytical Laboratory at NASA Goddard uses state-of-the-art laboratory analytical instrumentation in unconventional ways to examine extraterrestrial materials and tackle some of the big questions in astrobiology. This talk will discuss some of the instrumentation and techniques used for these unique samples, as well as some of our most interesting results. The talk will present two areas of particular interest in our laboratory: (1) the search for chiral excesses in meteoritic amino acids, which may help to explain the origin of homochirality in life on Earth; and (2) the detection of amino acids and amines in material returned by NASA's Stardust mission, which rendevouzed with a cornet and brought back cometary particles to the Earth.

  15. Polymerase chain reaction system using magnetic beads for analyzing a sample that includes nucleic acid

    Science.gov (United States)

    Nasarabadi, Shanavaz [Livermore, CA

    2011-01-11

    A polymerase chain reaction system for analyzing a sample containing nucleic acid includes providing magnetic beads; providing a flow channel having a polymerase chain reaction chamber, a pre polymerase chain reaction magnet position adjacent the polymerase chain reaction chamber, and a post pre polymerase magnet position adjacent the polymerase chain reaction chamber. The nucleic acid is bound to the magnetic beads. The magnetic beads with the nucleic acid flow to the pre polymerase chain reaction magnet position in the flow channel. The magnetic beads and the nucleic acid are washed with ethanol. The nucleic acid in the polymerase chain reaction chamber is amplified. The magnetic beads and the nucleic acid are separated into a waste stream containing the magnetic beads and a post polymerase chain reaction mix containing the nucleic acid. The reaction mix containing the nucleic acid flows to an analysis unit in the channel for analysis.

  16. A study on the generation of radioactive corrosion product at PWR for extended fuel cycle

    International Nuclear Information System (INIS)

    Min Chul Song; Kun Jai Lee

    2001-01-01

    Current nuclear power plant operating practice is to extend the time between refueling from a 12 month operating cycle to an 18-24 month period. This current to longer fuel cycles has complicated the dilemma of finding optimum pH range for the primary coolant chemistry. The International Commission on Radiological Protection (ICRP) in ICRP publication No. 60 recommends optimization of operator radiation exposure (ORE) in nuclear power plants. CRUD formed in the plants is the major source of ORE and its transport mechanism is not understood. To analyze the generation of CRUD at the extended fuel cycle, the COTRAN code, which was developed at the Korea Advanced Institute of Science and Technology (KAIST), was used. It predicts that the activity of CRUD decreases as the pH of the coolant increases. For the same period of different fuel cycles, as the operating fuel cycle duration is increased, the generation of the CRUD increases. In this paper, enriched boric acid (40% enriched 10 B concentration) for reactivity control is adopted as the required chemical shim rather than natural boric acid. The effect of the enriched boric acid (EBA) is that the neutron absorption capability of the chemical shim is maintained while decreasing the required boron and lithium concentration in the reactor coolant system. By employing enriched boric acid, the amounts of CRUD generated are reduced, because the high pH-operating period is extended. From the waste generation point of view, more filters or ion exchangers to remove CRUD are required and the amounts of waste are increased at the extended fuel cycle. (author)

  17. Flame retardant finishing of cotton fabric based on synergistic compounds containing boron and nitrogen.

    Science.gov (United States)

    Xie, Kongliang; Gao, Aiqin; Zhang, Yongsheng

    2013-10-15

    Boric acid and compound containing nitrogen, 2,4,6-tri[(2-hydroxy-3-trimethyl-ammonium)propyl]-1,3,5-triazine chloride (Tri-HTAC) were used to finish cotton fabric. The flame retardant properties of the finished cotton fabrics and the synergetic effects of boron and nitrogen elements were investigated and evaluated by limited oxygen index (LOI) method. The mechanism of cross-linking reaction among cotton fiber, Tri-HTAC, and boric acid was discussed by FTIR and element analysis. The thermal stability and surface morphology of the finished cotton fabrics were investigated by thermogravimetric analysis (TGA) and scanning electron microscope (SEM), respectively. The finishing system of the mixture containing boron and nitrogen showed excellent synergistic flame retardancy for cotton fabric. The cotton fabric finished with mixture system had excellent flame retardancy. The LOI value of the treated cotton fabric increased over 27.5. Tri-HTAC could form covalent bonds with cellulose fiber and boric acid. The flame retardant cotton fabric showed a slight decrease in tensile strength and whiteness. The surface morphology of flame retardant cotton fiber was smooth. Copyright © 2013 Elsevier Ltd. All rights reserved.

  18. Ammonia volatilization from coated urea forms

    Directory of Open Access Journals (Sweden)

    Carlos Antonio Costa do Nascimento

    2013-08-01

    Full Text Available Nitrogen fertilization is a major component of the cost of agricultural production, due to the high cost and low efficiency of fertilizers. In the case of urea, the low efficiency is mainly due to losses by volatilization, which are more pronounced in cultivation systems in which plant residues are left on the soil. The objective of this work was to compare the influence of urea coated with sulfur or boric acid and copper sulfate with conventional N fertilizers on N volatilization losses in sugar cane harvested after stubble burning. The sources urea, sulfur-coated urea, urea coated with boric acid and copper sulfate, as well as nitrate and ammonium sulfate, were tested at amounts containing N rates of 120 kg ha-1 N. The integration of new technologies in urea fertilization can reduce N losses by volatilization. These losses were most reduced when using nitrate and ammonium sulfate. The application of a readily acidified substance (boric acid to urea was more efficient in reducing volatilization losses and nutrient removal by sugar cane than that of a substance with gradual acidification (elemental sulfur.

  19. Contamination of the ground waters and surface waters by boron in Lerma Valley, NW-Argentina - an inventory

    International Nuclear Information System (INIS)

    Bundschuh, J.

    1992-01-01

    Ground- and surface waters in areas unaffected by pollution from borax and boric acid producing plants exhibit low boron concentrations of less than 300 μg B/l. Only at the boric acid plant 'Mineratea' is the groundwater contaminated, with up to 6200 μg B/l occurring within an area of 8 to 10 km 2 with more than 1000 μg boron/l. Even higher boron concentrations (up to 18 μg B/l) are present in polluted surface waters. Not the boron concentration in the irrigation water, but the absolute amount of boron added to the plants by irrigation is what determines plant toxicity. For the contaminated area of the boric acid 'Mineratea', characterized by boron concentrations of between 1000 and 6000 μg B/l, the maximal amounts of irrigation water that can be applied lies between 300 and 8 mm. In order to protect the local groundwater resoures from present and future contamination, environmental impact assessment on industrial projects in the area are required. In this way, the quality of the drinking and irrigation water can be guaranteed through suitable measures, without hindering further necessary industrial development of the region. (orig./UWA) [de

  20. Rapid determination of amino acids in biological samples using a monolithic silica column.

    Science.gov (United States)

    Song, Yanting; Funatsu, Takashi; Tsunoda, Makoto

    2012-05-01

    A high-performance liquid chromatography method in which fluorescence detection is used for the simultaneous determination of 21 amino acids is proposed. Amino acids were derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F) and then separated on a monolithic silica column (MonoClad C18-HS, 150 mm×3 mm i.d.). A mixture of 25 mM citrate buffer containing 25 mM sodium perchlorate (pH 5.5) and acetonitrile was used as the mobile phase. We found that the most significant factor in the separation was temperature, and a linear temperature gradient from 30 to 49°C was used to control the column temperature. The limits of detection and quantification for all amino acids ranged from 3.2 to 57.2 fmol and 10.8 to 191 fmol, respectively. The calibration curves for the NBD-amino acid had good linearity within the range of 40 fmol to 40 pmol when 6-aminocaproic acid was used as an internal standard. Using only conventional instruments, the 21 amino acids could be analyzed within 10 min. This method was found to be suitable for the quantification of the contents of amino acids in mouse plasma and adrenal gland samples.

  1. Impact of Sampling and Cellular Separation on Amino Acid Determinations in Drosophila Hemolymph.

    Science.gov (United States)

    Cabay, Marissa R; Harris, Jasmine C; Shippy, Scott A

    2018-04-03

    The fruit fly is a frequently used model system with a high degree of human disease-related genetic homology. The quantitative chemical analysis of fruit fly tissues and hemolymph uniquely brings chemical signaling and compositional information to fly experimentation. The work here explores the impact of measured chemical content of hemolymph with three aspects of sample collection and preparation. Cellular content of hemolymph was quantitated and removed to determine hemolymph composition changes for seven primary amine analytes. Hemolymph sampling methods were adapted to determine differences in primary amine composition of hemolymph collected from the head, antenna, and abdomen. Also, three types of anesthesia were employed with hemolymph collection to quantitate effects on measured amino acid content. Cell content was found to be 45.4 ± 22.1 cells/nL of hemolymph collected from both adult and larvae flies. Cell-concentrated fractions of adult, but not larvae, hemolymph were found to have higher and more variable amine content. There were amino acid content differences found between all three areas indicating a robust method to characterize chemical markers from specific regions of a fly, and these appear related to physiological activity. Methods of anesthesia have an impact on hemolymph amino acid composition related to overall physiological impact to fly including higher amino acid content variability and oxygen deprivation effects. Together, these analyses identify potential complications with Drosophila hemolymph analysis and opportunities for future studies to relate hemolymph content with model physiological activity.

  2. Determination of branched chain amino acids, methionine, phenylalanine, tyrosine and alpha-keto acids in plasma and dried blood samples using HPLC with fluorescence detection.

    Science.gov (United States)

    Kand'ár, Roman; Záková, Pavla; Jirosová, Jana; Sladká, Michaela

    2009-01-01

    The determination of branched chain amino acids [BCAA; valine (Val), leucine (Leu), isoleucine (Ile)], alpha-keto acids derived from BCAA [BCKA; alpha-ketoisovaleric acid (KIV), alpha-ketoisocaproic acid (KIC), alpha-ketomethylvaleric acid (KMV)], methionine (Met), phenylalanine (Phe) and tyrosine (Tyr) is currently the most reliable approach for the diagnosis of maple syrup urine disease (MSUD), hypermethioninemia, phenylketonuria (PKU) and tyrosinemia. The aim of this study was to develop rapid and simple HPLC methods for measurement of BCAA, Met, Phe, Tyr and BCKA in plasma and dried blood samples. Samples of peripheral venous blood with EDTA as anticoagulant were obtained from a group of healthy blood donors (n=70, 35 females, 27-41 years of age and 35 males, 28-43 years of age). Blood-spot samples from a group of newborns (n=80, 40 girls and 40 boys 3-5 days of age) were collected onto #903 Specimen Collection Paper and allowed to dry for at least 24 h before analysis. Prior to separation, the amino acids (AA) were derivatized with o-phthaldialdehyde (OPA) and BCKA with o-phenylenediamine (OPD). Reverse phase column chromatography (LiChroCart 125-4 Purospher RP-18e, 5 microm) was used for separation and fluorescence detection used to monitoring of effluent. For AA analysis, 25 mmol/L sodium hydrogenphosphate-methanol (90:10, v/v), pH 6.5+/-0.1 was used as mobile phase A and 100% methanol was used as mobile phase B. Measurement of BCKA used a mixture of methanol and deionized water (55:45, v/v) as mobile phase A and mobile phase B consisted of 100% methanol. Analytical performance of these methods was satisfactory for the determination of all AA and BCKA. The intra-assay and inter-assay coefficients of variation were below 10% and recovery ranged from 90%-110%. We have developed simple, rapid and selective HPLC methods with fluorescence detection for the determination of BCAA, Met, Phe, Tyr and BCKA in plasma and dried blood samples.

  3. Leaching of nuclear power reactor waste forms

    International Nuclear Information System (INIS)

    Endo, L.S.; Villalobos, J.P.; Miyamoto, H.

    1987-01-01

    The leaching tests for immobilized power reactor wastes carried out at IPEN are described. These wastes forms consist mainly of spent resins and boric acid concentrates solidified in ordinary Portland cement. All tests were conducted according to the ISO and IAEA recommendations. Three years leaching results are reported. The cesium diffuvity coefficients determined out of these results are about 1 x 10 -8 cm 2 /s for boric acid waste form and 9 x 10 -9 cm 2 /s for ion-exchange resin waste. Strontium diffusivity coefficients found are about 3 x 10 -11 cm 2 /s and 9 x 10 -11 cm 2 /s respectively. (Author) [pt

  4. The development of radioactive waste treatment technology(IV)

    International Nuclear Information System (INIS)

    Kim, Joon Hyung; Yim, Sung Paal; Lee, Kune Woo; Yoo, Jeong Woo; Kim, Young Min; Park, Seong Chul

    1992-03-01

    Following studies were performed in the project of development of radioactive waste treatment technology. 1) Treatment of radioactive borated liquid wastes by reverse osmosis : Separation characteristics of boric acid were estimated using cellulose acetate membrane and aromatic polyamide membrane. The performance of reverse osmosis process was evaluated in terms of boric acid recovery, radiochemical rejection, and membrane flux by operating variables such as applied pressure and feed concentration. 2) Oily waste treatment : The mathematical model to estimate oil removal efficiency is to be proposed at coalescence column. 3) Treatment of radioactive laundry waste 4) Comparison of evaporation and ion-exchange 5) State of the art of high integrity container. (Author)

  5. Influence of citric acid as chemical modifier for lead determination in dietary calcium supplement samples by graphite furnace atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Cezar Paz de Mattos, Julio; Medeiros Nunes, Adriane; Figueiredo Martins, Ayrton; Luiz Dressler, Valderi; Marlon de Moraes Flores, Erico

    2005-01-01

    Citric acid was used as a chemical modifier for Pb determination by graphite furnace atomic absorption spectrometry in dietary supplement samples (calcium carbonate, dolomite and oyster shell samples) and its efficiency was compared to the use of palladium. Pyrolysis and atomization curves were established without use of chemical modifier, with the addition of 20, 100 and 200 μg of citric acid, and with 3 μg of palladium. The citric acid modifier made possible the interference-free Pb determination in the presence of high concentrations of Ca and Mg nitrates. Acid sample digestion involving closed vessels (microwave-assisted and conventional heating) and acid attack using polypropylene vessels at room temperature were compared. All digestion procedures presented similar results for calcium carbonate and dolomite samples. However, for oyster shell samples accurate results were obtained only with the use of closed vessel systems. Analyte addition and matrix-matched standards were used for calibration. The characteristic mass for Pb using citric acid and palladium were 16 and 25 pg, respectively. The relative standard deviation (RSD) was always less than 5% when citric acid was used. The relative and absolute limits of detection were 0.02 μg g -1 and 8 pg with citric acid and 0.1 μg g -1 and 44 pg with the Pd modifier, respectively (n = 10, 3σ). The recovery of Pb in spiked calcium supplement samples (10 μg l -1 ) was between 98% and 105%. With the use of 100 μg of citric acid as chemical modifier, problems such as high background absorption and high RSD values were minimized in comparison to the addition of 3 μg of palladium

  6. Volumetric and chemical control auxiliary circuit for a PWR primary circuit

    International Nuclear Information System (INIS)

    Costes, D.

    1990-01-01

    The volumetric and chemical control circuit has an expansion tank with at least one water-steam chamber connected to the primary circuit by a sampling pipe and a reinjection pipe. The sampling pipe feeds jet pumps controlled by valves. An action on these valves and pumps regulates the volume of the water in the primary circuit. A safety pipe controlled by a flap automatically injects water from the chamber into the primary circuit in case of ruptures. The auxiliary circuit has also systems for purifying the water and controlling the boric acid and hydrogen content [fr

  7. The effects of different additives in electrolyte of AGM batteries on self-discharge

    Energy Technology Data Exchange (ETDEWEB)

    Yazd, M. Safari; Molazemi, A. [Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, P.O. Box 91775-1111 (Iran); Moayed, M.H. [Metallurgical and Materials Engineering Department, Faculty of Engineering, Ferdowsi University of Mashhad, P.O. Box 91775-1111 (Iran)

    2006-07-14

    Hydrogen and oxygen evolution at the negative and positive electrodes in AGM batteries are the main reasons of self-discharging. The self-discharge of five AGM batteries was investigated by measuring different potential between two electrodes during 48 days. Five different battery electrolytes were used including 35% (w/w) H{sub 2}SO{sub 4} without additives and the remaining contain 7.1, 9.94, and 21.3gl{sup -1} sodium sulfate, 4gl{sup -1} boric acid, 3gl{sup -1} citric acid, and finally 0.7 and 1gl{sup -1} stearic acid except one containing boric acid that the concentration of H{sub 2}SO{sub 4} was 36% (w/w). The results revealed that the rate of self-discharge for battery without additive was 0.01Vday{sup -1}. The battery with boric acid showed the lowest rate of self-discharge with 0.0025Vday{sup -1}. It was also found that stearic and citric acids are comparatively appropriate additives for decreasing the self-discharge. They caused a decrease of the self-discharge rate to 0.005 and 0.0075Vday{sup -1} on appropriate concentration, respectively. In compared to other additives, sodium sulfate showed to be not an appropriate additive for decreasing battery self-discharging. The rate of 0.03Vday{sup -1} of self-discharging was obtained for the battery containing all selected concentration of sodium sulfate during first 4 days of measuring. (author)

  8. Comparison of alkaline fusion and acid digestion methods for the determination of rhenium in rock and soil samples by ICP-MS

    International Nuclear Information System (INIS)

    Uchida, Shigeo; Tagami, Keiko; Tabei, Ken

    2005-01-01

    A simple acid digestion method was studied in order to analyze many samples at once to understand Re behavior in the terrestrial environment, because, under normal laboratory conditions, digestion methods generally used, such as Carius tube digestions, Teflon vessel digestions and alkaline fusions, can handle only a small number of samples at one time to ensure complete sample digestion. In this study, the Re results for reference materials (RMs) obtained by the acid digestion method were compared with those by the alkaline fusion digestion method to get applicability of the acid digestion method for Re determination in soil by inductively coupled plasma mass spectrometry. Alkaline fusion was chosen for the comparison because it is known to have the highest capability to dissolve Re in geological materials among digestion methods. The average total Re recoveries measured using the 185 Re spike for RMs, such as rock, soil and sediment, were 90.6 ± 4.0% for alkaline fusion and 92.2 ± 7.3% for acid digestion, showing no differences between them. However, Re results obtained by the acid digestion method were usually slightly lower than those by the alkaline fusion (Student's t-test, P -1 , the acid digestion method could dissolve about 80% of the sample Re. Although the acid digestion method is unable to dissolve all Re in the sample, however, the Re discharged to soils could be more extractable than the Re in the dissolution-resistant part; thus, the acid digestion method could be useful for obtaining Re levels in soil samples

  9. Determination of boron in sea water by atomic absorption spectrophotometry

    International Nuclear Information System (INIS)

    Horta, A.M.T.C.; Curtius, A.J.

    1978-01-01

    The chelation-extraction of boric acid with are acid solution of 2-ethyl-1,3 hexanediol in methy1-isobutye-ketone is studied. By this way a simple, quick and precise method for boron determination can be obtained [pt

  10. A bench-top automated workstation for nucleic acid isolation from clinical sample types.

    Science.gov (United States)

    Thakore, Nitu; Garber, Steve; Bueno, Arial; Qu, Peter; Norville, Ryan; Villanueva, Michael; Chandler, Darrell P; Holmberg, Rebecca; Cooney, Christopher G

    2018-04-18

    Systems that automate extraction of nucleic acid from cells or viruses in complex clinical matrices have tremendous value even in the absence of an integrated downstream detector. We describe our bench-top automated workstation that integrates our previously-reported extraction method - TruTip - with our newly-developed mechanical lysis method. This is the first report of this method for homogenizing viscous and heterogeneous samples and lysing difficult-to-disrupt cells using "MagVor": a rotating magnet that rotates a miniature stir disk amidst glass beads confined inside of a disposable tube. Using this system, we demonstrate automated nucleic acid extraction from methicillin-resistant Staphylococcus aureus (MRSA) in nasopharyngeal aspirate (NPA), influenza A in nasopharyngeal swabs (NPS), human genomic DNA from whole blood, and Mycobacterium tuberculosis in NPA. The automated workstation yields nucleic acid with comparable extraction efficiency to manual protocols, which include commercially-available Qiagen spin column kits, across each of these sample types. This work expands the scope of applications beyond previous reports of TruTip to include difficult-to-disrupt cell types and automates the process, including a method for removal of organics, inside a compact bench-top workstation. Copyright © 2018 Elsevier B.V. All rights reserved.

  11. Extraction of methylmercury from tissue and plant samples by acid leaching

    Energy Technology Data Exchange (ETDEWEB)

    Hintelmann, Holger; Nguyen, Hong T. [Trent University, Chemistry Department, Peterborough, ON (Canada)

    2005-01-01

    A simple and efficient extraction method based on acidic leaching has been developed for measurement of methylmercury (MeHg) in benthic organisms and plant material. Methylmercury was measured by speciated isotope-dilution mass spectrometry (SIDMS), using gas chromatography interfaced with inductively coupled plasma mass spectrometry (GC-ICP-MS). Reagent concentration and digestion temperature were optimized for several alkaline and acidic extractants. Recovery was evaluated by addition of MeHg enriched with CH{sub 3}{sup 201}Hg{sup +}. Certified reference materials (CRM) were used to evaluate the efficiency of the procedure. The final digestion method used 5 mL of 4 mol L{sup -1} HNO{sub 3} at 55 C to leach MeHg from tissue and plant material. The digest was further processed by aqueous phase ethylation, without interference with the ethylation step, resulting in 96{+-}7% recovery of CH{sub 3}{sup 201}Hg{sup +} from oyster tissue and 93{+-}7% from pine needles. Methylmercury was stable in this solution for at least 1 week and measured concentrations of MeHg in CRM were statistically not different from certified values. The method was applied to real samples of benthic invertebrates and inter-laboratory comparisons were conducted using lyophilized zooplankton, chironomidae, and notonectidae samples. (orig.)

  12. Inverse-Frontal Chromatography studies on enrichment of Boron-10 using quaternery 4-vinylpyridine-divinylbenzene resin

    International Nuclear Information System (INIS)

    Bejawada, Venki; Mohapatra, C.; Rao, A.S.; Prasad, K.L.; Murthy, P.K.; Rao, A.K.; Singh, H.P.; Vithal, G.K.; Kumar, Sangita D.

    2014-01-01

    In order to enrich 10 B, band migration of boric acid-mannitol with hydrochloric acid solution was performed by inverse frontal chromatography on a porous, 25% crosslinked, 38% quaternized 4-vinylpyridine-divinylbenzene resin (py-resin). The work was initiated to replace the existing strong base anion exchange resin type-II (SBA-II) which is used in Boron Enrichment Plant (BEP) of heavy water plant Manuguru. Before its application in BEP, it is mandatory to evaluate py-resin for its performance. The studies showed that maximum of 40% 10 B enrichment observed after 13 m band movement and there was no further improvement, hence profile sampling carried out after 28 m. (author)

  13. Synthesis and characterization of boron trifluoride (B F[sub 3]). Sintese e caracterizacao de trifluoreto de boro (BF[sub 3])

    Energy Technology Data Exchange (ETDEWEB)

    Bastos, E T.R.; Umeda, K; Echternacht, M V; Silva, E.F. da.

    1994-08-01

    High purity boron trifluoride (B F[sub 3]) has been prepared from reaction of ammonium fluorborate and boron oxide in concentrated sulfuric acid. Fluorborate was synthesized by reaction of ammonium bi fluoride and boric acid produced from enrichment plant. (author).

  14. Study of sample preparation for quantitative analysis of amino acids in human sweat by liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Delgado-Povedano, M M; Calderón-Santiago, M; Priego-Capote, F; Luque de Castro, M D

    2016-01-01

    The determination of physiological levels of amino acids is important to aid in the diagnosis and treatment of several diseases and nutritional status of individuals. Amino acids are frequently determined in biofluids such as blood (serum or plasma) and urine; however, there are less common biofluids with different concentration profiles of amino acids that could be of interest. One of these biofluids is sweat that can be obtained in a non-invasive manner and is characterized by low complex composition. The analysis of amino acids in human sweat requires the development of sample preparation strategies according to the sample matrix and small collected volume. The influence of sample preparation on the quantitative analysis of amino acids in sweat by LC-MS/MS has been assessed through a comparison between two strategies: dilution of sweat and centrifugal microsolid-phase extraction (c-μSPE). In both cases, several dilution factors were assayed for in-depth knowledge of the matrix effects, and the use of c-μSPE provided the best results in terms of accuracy. The behavior of the target analytes was a function of the dilution factor, thus providing a pattern for sample preparation that depended on the amino acid to be determined. The concentration of amino acids in sweat ranges between 6.20 ng mL(-1) (for homocysteine) and 259.77 µg mL(-1) (for serine) with precision, expressed as relative standard deviation, within 1.1-21.4%. Copyright © 2015 Elsevier B.V. All rights reserved.

  15. PENGGUNAAN PENGAWET DAN PEMANIS BUATAN PADA PANGAN JAJANAN ANAK SEKOLAH (PJAS DI WILAYAH KABUPATEN KULON PROGO-DIY (The Use of Preservatives and Artificial Sweeteners in Elementary School-Food in Kulon Progo District of DIY Province

    Directory of Open Access Journals (Sweden)

    Chatarina Wariyah

    2013-08-01

    Full Text Available School-food (SF is processed-foods sold by vendor in the elementary school. Recently, many SF has been found to contain excessive food additives and used hazardous substances those are prohibited i.e. formalin, boric acid and rhodamin. The prebious survey showed that the considerations for buying food of most people in Kulon Progo District of DIY province were price, taste, appearance, and were not of the quality and nutrition. The purpose of this research was to determine the SF profile in Kulon Progo District, especially those used excessive food additive (preservative and artificial sweetener, SF with hazardous substances, and the relation between SF condition and the education level of the vendor. The sampling method used Proportionate Random Sampling consists of two stages, namely: 1 sampling to determine the sub-district samples and 2 sampling to determine the amount of the elementary-school of each sub-district for SF sampling. The data were collected by direct observation, interview and experimental method. Analysis of sodium benzoat and sorbic acid, saccharin, sodium cyclamate, and unrecommended/hazardous substances were conducted in BBPOM Laboratory and BLK of Yoyakarta. The data were statistically analyzed by statistic-descriptive and processed with microsoft excell and SPSS for window version 13 for Spearman correlative test.The research showed that SF at the elementary school in Kulon Progo District indicated to contain excessive food additives and hazardous substances. There were 4% samples containing excessive sodium benzoat, sorbic acid and 8% samples containing excessive artificial sweetener of sodium cyclamate. SF with boric acid was 3% samples (cilok, sosis, kerupuk rambak and with formalin was 1% samples (burjo,cimol. There was a significant correlation between the education level of the SF vendor with knowledge about formalin, boric acid and artificial sweetener. Keywords: School-food, food-additives, unrecommended

  16. Sugar and acid interconversion in tomato fruits based on biopsy sampling of locule gel and pericarp tissue

    NARCIS (Netherlands)

    Schouten, R.E.; Woltering, E.J.; Tijskens, L.M.M.

    2016-01-01

    This study deals with quantifying sugar and acids levels important for the perceived taste of tomatoes (Solanum lycopersicum). Sugar and acids levels were measured repeatedly on the same tomato using tissue samples obtained with a biopsy needle in combination with HPLC protocols. Biopsies of

  17. Loss of ammonia from nitrogen fertilizers applied to maize and soybean straw

    Directory of Open Access Journals (Sweden)

    Letícia de Abreu Faria

    2013-08-01

    Full Text Available In Brazilian agriculture, urea is the most commonly used nitrogen (N source, in spite of having the disadvantage of losing considerable amounts of N by ammonia-N volatilization. The objectives of this study were to evaluate: N lossby ammonia volatilization from: [urea coated with copper sulfate and boric acid], [urea coated with zeolite], [urea+ammonium sulfate], [urea coated with copper sulfate and boric acid+ammonium sulfate], [common urea] and [ammonium nitrate]; and the effect of these N source son the maize yield in terms of amount and quality. The treatments were applied to the surface of a soil under no-tillage maize, in two growing seasons. The first season (2009/2010 was after a maize crop (maize straw left on the soil surface and the second cycle (2012/2011 after a soybean crop. Due to the weather conditions during the experiments, the volatilization of ammonia-N was highest in the first four days after application of the N sources. Of all urea sources, under volatilization-favorable conditions, the loss of ammonia from urea coated with copper sulfate and boric acid was lowest, while under high rainfall, the losses from the different urea sources was similar, i.e., an adequate rainfall was favorablet o reduce volatilization. The ammonia volatilization losses were greatest in the first four days after application. Maize grain yield differed due to N application and in the treatments, but this was only observed with cultivation of maize crop residues in 2009/2010. The combination of ammonium+urea coated with copper sulfate and boric acid optimized grain yield compared to the other urea treatments. The crude protein concentration in maize was not influenced by the technologies of urea coating.

  18. Immobilized laccase mediated dye decolorization and transformation pathway of azo dye acid red 27.

    Science.gov (United States)

    Chhabra, Meenu; Mishra, Saroj; Sreekrishnan, Trichur Ramaswamy

    2015-01-01

    Laccases have good potential as bioremediating agents and can be used continuously in the immobilized form like many other enzymes. In the present study, laccase from Cyathus bulleri was immobilized by entrapment in Poly Vinyl Alcohol (PVA) beads cross-linked with either nitrate or boric acid. Immobilized laccase was used for dye decolorization in both batch and continuous mode employing a packed bed column. The products of degradation of dye Acid Red 27 were identified by LC MS/MS analysis. The method led to very effective (90%) laccase immobilization and also imparted significant stability to the enzyme (more than 70% after 5 months of storage at 4°C). In batch decolorization, 90-95% decolorization was achieved of the simulated dye effluent for up to 10-20 cycles. Continuous decolorization in a packed bed bioreactor led to nearly 90% decolorization for up to 5 days. The immobilized laccase was also effective in decolorization and degradation of Acid Red 27 in the presence of a mediator. Four products of degradation were identified by LC-MS/MS analysis. The immobilized laccase in PVA-nitrate was concluded to be an effective agent in treatment of textile dye effluents.

  19. A highly sensitive kinetic spectrophotometric method for the determination of ascorbic Acid in pharmaceutical samples.

    Science.gov (United States)

    Shishehbore, Masoud Reza; Aghamiri, Zahra

    2014-01-01

    In this study, a new reaction system for quantitative determination of ascorbic acid was introduced. The developed method is based on inhibitory effect of ascorbic acid on the Orange G-bromate system. The change in absorbance was followed spectrophotometrically at 478 nm. The dependence of sensitivity on the reaction variables including reagents concentration, temperature and time was investigated. Under optimum experimental conditions, calibration curve was linear over the range 0.7 - 33.5 μg mL(-1) of ascorbic acid including two linear segments and the relative standard deviations (n = 6) for 5.0 and 20.0 μg mL(-1) of ascorbic acid were 1.08 and 1.02%, respectively. The limit of detection was 0.21 μg mL(-) (1) of ascorbic acid. The effect of diverse species was also investigated. The developed method was successfully applied for the determination of ascorbic acid in pharmaceutical samples. The results were in a good agreement with those of reference method.

  20. Headspace solid-phase microextraction with 1-pyrenyldiazomethane on-fibre derivatisation for analysis of fluoroacetic acid in biological samples.

    Science.gov (United States)

    Sporkert, Frank; Pragst, Fritz; Hübner, Sandra; Mills, Graham

    2002-05-25

    A new and in part automated headspace solid-phase microextraction method for quantitative determination of the highly toxic rodenticide fluoroacetic acid (FAA) in serum and other biological samples has been developed. FAA and deuterated acetic acid (internal standard) were extracted from acidified samples by a StableFlex divinylbenzene-Carboxen on polydimethylsiloxane fibre. The acids were derivatised on the fibre in-situ with 1-pyrenyldiazomethane and detected using gas chromatography-mass spectrometry with electron impact ionisation and selected ion monitoring. The calibration curve for FAA in serum was linear over the range from 0.02 to 5 microg/ml, with limits of detection and quantification of 0.02 and 0.07 microg/ml, respectively. The method was also tested with spiked whole blood, urine, stomach contents and kidney samples. It was sufficiently reliable, reproducible and sensitive for use in routine forensic toxicology applications.

  1. Enhancement of virulence of bacillus thuringiensis and serratia marcescens by chemicals

    International Nuclear Information System (INIS)

    Khan, K. A.

    2006-01-01

    Studies were conducted on the enhancement of pathogenicity of Bacillus thuringiensis by 1% boric acid against various species of termites. The increase in virulence of Serratia marcescens by 1% potassium chloride or 1% Sodium citrate against the workers of M. championi has also been established. The increase in virulence is confirmed by the enhancement ratio, which are ranging from about 1.5 to 1.8 for Bacillus thuringiensis and 1.3 to 1.6 for Serratia marcescens. It was also noted that 1% boric acid alone was found toxic to various species of termites. However, Potassium chloride and Sodium citrate in a concentration of 1% were non-toxic to the workers of M. championi. (author)

  2. Coolant circuit water chemistry of the Paks Nuclear Power Plant

    International Nuclear Information System (INIS)

    Tilky, Peter; Doma, Arpad

    1985-01-01

    The numerous advantages of the proper selection of water chemistry parameters including low corrosion rate of the structural materials, hence the low-level activity build-up, depositions, radiation doses were emphasized. Major characteristics of water chemistry applied to the primary coolant of pressurized water reactors including neutral, slightly basic and strong basic ones are discussed. Boric acid is widely used to control reactivity. Primary coolant water chemistry of WWER type reactors which is based on the addition of ammonia and potassium hydroxide to boric acid is compared with that of other reactors. The demineralization of the total condensate of the steam turbines became a general trend in the water chemistry of the secondary coolant circuits. (V.N.)

  3. Amino acid analysis in physiological samples by GC-MS with propyl chloroformate derivatization and iTRAQ-LC-MS/MS.

    Science.gov (United States)

    Dettmer, Katja; Stevens, Axel P; Fagerer, Stephan R; Kaspar, Hannelore; Oefner, Peter J

    2012-01-01

    Two mass spectrometry-based methods for the quantitative analysis of free amino acids are described. The first method uses propyl chloroformate/propanol derivatization and gas chromatography-quadrupole mass spectrometry (GC-qMS) analysis in single-ion monitoring mode. Derivatization is carried out directly in aqueous samples, thereby allowing automation of the entire procedure, including addition of reagents, extraction, and injection into the GC-MS. The method delivers the quantification of 26 amino acids. The isobaric tagging for relative and absolute quantification (iTRAQ) method employs the labeling of amino acids with isobaric iTRAQ tags. The tags contain two different cleavable reporter ions, one for the sample and one for the standard, which are detected by fragmentation in a tandem mass spectrometer. Reversed-phase liquid chromatography of the labeled amino acids is performed prior to mass spectrometric analysis to separate isobaric amino acids. The commercial iTRAQ kit allows for the analysis of 42 physiological amino acids with a respective isotope-labeled standard for each of these 42 amino acids.

  4. Insights into the Mechanisms Underlying Boron Homeostasis in Plants

    Directory of Open Access Journals (Sweden)

    Akira Yoshinari

    2017-11-01

    Full Text Available Boron is an essential element for plants but is toxic in excess. Therefore, plants must adapt to both limiting and excess boron conditions for normal growth. Boron transport in plants is primarily based on three transport mechanisms across the plasma membrane: passive diffusion of boric acid, facilitated diffusion of boric acid via channels, and export of borate anion via transporters. Under boron -limiting conditions, boric acid channels and borate exporters function in the uptake and translocation of boron to support growth of various plant species. In Arabidopsis thaliana, NIP5;1 and BOR1 are located in the plasma membrane and polarized toward soil and stele, respectively, in various root cells, for efficient transport of boron from the soil to the stele. Importantly, sufficient levels of boron induce downregulation of NIP5;1 and BOR1 through mRNA degradation and proteolysis through endocytosis, respectively. In addition, borate exporters, such as Arabidopsis BOR4 and barley Bot1, function in boron exclusion from tissues and cells under conditions of excess boron. Thus, plants actively regulate intracellular localization and abundance of transport proteins to maintain boron homeostasis. In this review, the physiological roles and regulatory mechanisms of intracellular localization and abundance of boron transport proteins are discussed.

  5. Borate compound content reduction in liquid radioactive waste from nuclear power plants with VVER reactor

    International Nuclear Information System (INIS)

    Szalo, A.; Zatkulak, M.

    2000-01-01

    This paper describes the current status of liquid waste (evaporator concentrates) inventory at V-1 and V-2 NPPs in Jaslovske Bohunice and the intention to separate boron from them with respect to waste minimisation and improvement of physical and chemical properties for further waste treatment and conditioning. Preliminary results of laboratory experiments concerned to borate crystallisation after pH adjustment with nitric or formic acid performed in the 1998 are given. At the present time laboratory experiments continuing - next acids, coagulation with carbon oxide, electrolytic process, ion exchange resin, study of decontamination factors, immobilization of boric acid, decrease radioactivity, purification of boron-contained compounds. Slovenske Elektrarne have accumulated 7,000 m 3 of evaporator concentrates containing 100-180 g/l borate. In order to make more storage space available, it is proposed to remove some of the borate in the liquor by precipitation as sodium tetraborate and immobilise in either cement of bitumen. The supernate can be further volume reduced by evaporation and returned to the tanks. Slovenske Elektrarne are currently evaluating acid addition to the pH 12-13 concentrate to reduce the borate solubility. However, this adds to the salt burden of the waste through this chemical addition -thus creating future increases in conditioning and disposal costs. Boric acid is used in pressurized water as a soluble neutron poison to control reactivity and also to assure a safety margin in the spent fuel pool and during refuelling operations. Boric acid is also present in the water reserved for injection into the reactor in the event of postulated accidents. (author)

  6. Poster 34. Monitoring of soluble species in the NPTEC SCEPTRE loop

    International Nuclear Information System (INIS)

    Eley, C.D.; Thomas, D.M.; Libaert, D.F.; Cattell, R.A.; Garbett, K.; Woolsey, I.S.

    1992-01-01

    Soluble transition metal ion and other species were measured in the coolant of the SCEPTRE Loop under PWR primary circuit conditions typical of the hot functional test and normal load operation. Good consistency between lines was observed for stainless steel sample lines with relatively high linear flow rates, rapid cooling to near ambient temperature and PTFE lining downstream of the cooler. Phenomenological conditioning times of the order of 100 hours for soluble transition metal species were determined for this type of sampling system. The behaviour of soluble transition metal species in a static, aerated stainless steel tank containing boric acid solutions was also investigated. (author)

  7. Gravimetric screening method for fungal decay of paper: inoculation with Trametes versicolor.

    Science.gov (United States)

    Råberg, Ulrika; Hafrén, Jonas

    2009-10-01

    The European standard test EN 113 for fungal degradation of solid wood has been adapted for degradation of paper by white rot fungus (Trametes versicolor). Fungal degradation of paper sheets may potentially be used for screening different wood preservatives on paper instead of solid wood. The paper samples showed higher relative mass losses compared to wood, and samples pretreated with boric acid, copper sulfate and polymerized linseed oil were successfully tested for biodegradation using the paper sheet method. The results on paper degradation were compared with wood, both as wood blocks (according to standard test) and wood cut in sections forming layered structures mimicking paper layers.

  8. Boron evaporation in thermally-driven seawater desalination: Effect of temperature and operating conditions

    KAUST Repository

    Alpatova, Alla; Alsaadi, Ahmad Salem; Ghaffour, NorEddine

    2018-01-01

    The volatilization of boron in thermal desalination processes, namely multi-stage flash (MSF) and air-gap membrane distillation (AGMD) was investigated for the first time. This phenomenon was observed at feed temperatures above 55 °C in both studied processes. In simulated MSF process with two feeds, model boric acid and Red Sea water, boron concentration in distillate increased with feed temperature increase from 55 °C to 104 °C because of the increase in boric acid vapor pressure. Salinity and pH were the main factors controlling boron evaporation. The achieved boron concentrations in simulated MSF process were consistent with those measured in distillate samples collected from commercial MSF plants. The AGMD process also revealed a strong influence of operating temperature on boron removal. However, unlike MSF process, the boron concentration in AGMD permeate decreased with the feed temperature increase from 55 °C to 80 °C due probably to increase in vapor production and corresponding permeate dilution. When AGMD was operated in concentrating mode at a constant feed temperature of 80 °C, permeate boron concentration increased with process time due to concentration polarization and membrane fouling. A 10% flux decline observed after 21 h was attributed to CaCO scaling on the membrane surface.

  9. The 10B(n,α)7Li reaction in PWR coolants: calculations of the effect on coolant pH and on decreases in 10B isotopic fractions

    International Nuclear Information System (INIS)

    Polley, M.V.

    1988-07-01

    Boron is used as a chemical shim in PWRs for reactivity control and is added in the form of boric acid to the primary coolant. The 10 B(n,α) 7 Li reaction leads to a continuous increase in 7 Li in the primary coolant and to a continuous decrease in 10 B the isotope of boron responsible for control of reactivity. The rate of increase in coolant pH due to 7 Li production is calculated for the Sizewell 'B' PWR to enable judgements to be made on the frequency of sampling and removal of lithium required to maintain the pH of the primary coolant within the desired limits. Calculations are contrasted for the cases of natural boron and 100% 10 B chemical shims, for both a normal cycle and an extended 18 month cycle. Calculations of 10 B depletion over 30 years of operation as a function of the quantity of boron discharged to waste are also presented. 10 B isotopic fractions are calculated for the reactor coolant (RC), boric acid tanks (BATs) and refuelling water storage tank (RWST) assuming rapid mixing of BAT and RC boron for tritium control and other reasons. Such predictions enable assessments of the reactor physics implications of 10 B consumption to be made. (author)

  10. Boron evaporation in thermally-driven seawater desalination: Effect of temperature and operating conditions

    KAUST Repository

    Alpatova, Alla

    2018-03-26

    The volatilization of boron in thermal desalination processes, namely multi-stage flash (MSF) and air-gap membrane distillation (AGMD) was investigated for the first time. This phenomenon was observed at feed temperatures above 55 °C in both studied processes. In simulated MSF process with two feeds, model boric acid and Red Sea water, boron concentration in distillate increased with feed temperature increase from 55 °C to 104 °C because of the increase in boric acid vapor pressure. Salinity and pH were the main factors controlling boron evaporation. The achieved boron concentrations in simulated MSF process were consistent with those measured in distillate samples collected from commercial MSF plants. The AGMD process also revealed a strong influence of operating temperature on boron removal. However, unlike MSF process, the boron concentration in AGMD permeate decreased with the feed temperature increase from 55 °C to 80 °C due probably to increase in vapor production and corresponding permeate dilution. When AGMD was operated in concentrating mode at a constant feed temperature of 80 °C, permeate boron concentration increased with process time due to concentration polarization and membrane fouling. A 10% flux decline observed after 21 h was attributed to CaCO scaling on the membrane surface.

  11. An integrated paper-based sample-to-answer biosensor for nucleic acid testing at the point of care.

    Science.gov (United States)

    Choi, Jane Ru; Hu, Jie; Tang, Ruihua; Gong, Yan; Feng, Shangsheng; Ren, Hui; Wen, Ting; Li, XiuJun; Wan Abas, Wan Abu Bakar; Pingguan-Murphy, Belinda; Xu, Feng

    2016-02-07

    With advances in point-of-care testing (POCT), lateral flow assays (LFAs) have been explored for nucleic acid detection. However, biological samples generally contain complex compositions and low amounts of target nucleic acids, and currently require laborious off-chip nucleic acid extraction and amplification processes (e.g., tube-based extraction and polymerase chain reaction (PCR)) prior to detection. To the best of our knowledge, even though the integration of DNA extraction and amplification into a paper-based biosensor has been reported, a combination of LFA with the aforementioned steps for simple colorimetric readout has not yet been demonstrated. Here, we demonstrate for the first time an integrated paper-based biosensor incorporating nucleic acid extraction, amplification and visual detection or quantification using a smartphone. A handheld battery-powered heating device was specially developed for nucleic acid amplification in POC settings, which is coupled with this simple assay for rapid target detection. The biosensor can successfully detect Escherichia coli (as a model analyte) in spiked drinking water, milk, blood, and spinach with a detection limit of as low as 10-1000 CFU mL(-1), and Streptococcus pneumonia in clinical blood samples, highlighting its potential use in medical diagnostics, food safety analysis and environmental monitoring. As compared to the lengthy conventional assay, which requires more than 5 hours for the entire sample-to-answer process, it takes about 1 hour for our integrated biosensor. The integrated biosensor holds great potential for detection of various target analytes for wide applications in the near future.

  12. Determination of 35S-aminoacyl-transfer ribonucleic acid specific radioactivity in small tissue samples

    International Nuclear Information System (INIS)

    Samarel, A.M.; Ogunro, E.A.; Ferguson, A.G.; Lesch, M.

    1981-01-01

    Rate determination of protein synthesis utilizing tracer amino acid incorporation requires accurate assessment of the specific radioactivity of the labeled precursor aminoacyl-tRNA pool. Previously published methods presumably useful for the measurement of any aminoacyl-tRNA were unsuccessful when applied to [ 35 S]methionine, due to the unique chemical properties of this amino acid. Herein we describe modifications of these methods necessary for the measurement of 35 S-aminoacyl-tRNA specific radioactivity from small tissue samples incubated in the presence of [ 35 S]methionine. The use of [ 35 S]methionine of high specific radioactivity enables analysis of the methionyl-tRNA from less than 100 mg of tissue. Conditions for optimal recovery of 35 S-labeled dansyl-amino acid derivatives are presented and possible applications of this method are discussed

  13. Boron-containing acids: preliminary evaluation of acute toxicity and access to the brain determined by Raman scattering spectroscopy.

    Science.gov (United States)

    Soriano-Ursúa, Marvin A; Farfán-García, Eunice D; López-Cabrera, Yessica; Querejeta, Enrique; Trujillo-Ferrara, José G

    2014-01-01

    Boron-containing compounds (BCCs), particularly boron containing acids (BCAs), have become attractive moieties or molecules in drug development. It has been suggested that when functional groups with boron atoms are added to well-known drugs, the latter are conferred with greater potency and efficacy in relation to their target receptors. However, the use of BCAs in drug development is limited due to the lack of a toxicological profile. Consequently, the aim of the present study was to evaluate the acute toxicity of boric and boronic acids. Thus, a determination was made of the lethal dose (LD50) of test compounds in male CD1 mice, as well as the effective dose required to negatively affect spontaneous motor activity and to produce notable behavioral abnormalities. After treatment of animals at different doses, macroscopic observations were made from a necropsy, and Raman scattering spectroscopic studies were carried out on brain tissue samples. In general, the results show that most of the tested BCAs have very low toxicity, evidenced by the high doses required to induce notable toxic effects (greater than 100 mg/kg of body weight for all compounds, except for 3-thyenilboronic acid). Such toxic effects, presumably mediated by action on the CNS, include eye damage, gastrointestinal effects (e.g., gastric-gut dilatation and fecal retention), sedation, hypnosis and/or trembling. This preliminary toxicological profile suggests that BCAs can be considered potential therapeutic agents or moieties to be added to other compounds in the development of new drugs. Future studies are required to explore possible chronic toxicity of BCCs. Copyright © 2013 Elsevier Inc. All rights reserved.

  14. FTA Cards for Preservation of Nucleic Acids for Molecular Assays: A Review on the Use of Cytologic/Tissue Samples.

    Science.gov (United States)

    da Cunha Santos, Gilda

    2018-03-01

    - Traditional methods for storing histologic and cytologic specimens for future use in molecular assays have consisted of either snap-freezing with cryopreservation or formalin-fixing, paraffin-embedding the samples. Although snap-freezing with cryopreservation is recommended for better preservation of nucleic acids, the infrastructure and space required for archiving impose challenges for high-volume pathology laboratories. Cost-effective, long-term storage at room temperature; relatively easy shipment; and standardized handling can be achieved with formalin-fixed, paraffin-embedded samples, but formalin fixation induces fragmentation and chemical modification of nucleic acids. Advances in next-generation sequencing platforms, coupled with an increase in diagnostic, prognostic, and predictive molecular biomarkers have created a demand for high-quality nucleic acids. To address issues of the quality of nucleic acid and logistics in sample acquisition, alternatives for specimen preservation and long-term storage have been described and include novel universal tissue fixatives, stabilizers, and technologies. - To collect, retrieve, and review information from studies describing the use of nucleic acids recovered from cytologic/tissue specimens stored on Flinders Technology Associates (FTA, GE Whatman, Maidstone, Kent, United Kingdom) cards for downstream molecular applications. - An electronic literature search in the PubMed (National Center for Biotechnology Information, Bethesda, Maryland) database allowed the selection of manuscripts addressing the use of FTA cards for storage of cytologic samples for molecular analysis. Only articles published in English were retrieved. - The use of FTA cards is a versatile method for fostering multicenter, international collaborations and clinical trials that require centralized testing, long-distance shipment, and high-quality nucleic acids for molecular techniques. Studies with controlled temperature are required to test the

  15. COMBUSTION PROPERTIES OF EUCALYPTUS WOOD

    Directory of Open Access Journals (Sweden)

    Yalçın ÖRS

    1999-03-01

    Full Text Available In this study, the combustion properties of some impregnation materials (abiotic and biotic factors used for eucalyptus wood in interior or exterior environments were investigated. The experimental samples were prepared from Eucalyptus wood based on ASTM-D-1413-76 Tanalith-CBC, boric acid, borax, vacsol-WR, immersol-WR, polyethylen glycole-400 and ammonium sulphate were used as an impregnation material. The results indicated that, vacuum treatment on Eucalyptus gave the lowest retention value of salts. Compounds containing boron+salt increased fire resistance however water repellents decreased the wood flammability.

  16. Chemistry aspects of the Falcon programme

    International Nuclear Information System (INIS)

    Beard, A.M.; Bennett, P.J.; Benson, C.G.; Sabathier, F.

    1990-12-01

    Experiments have been conducted in the Falcon facility to study the interaction of fission product vapours released from simulant and trace-irradiated fuel samples with bulk-materials aerosol such as control rod alloy and boric acid. These experiments were designed in collaboration with computer code specialists to represent, as closely as possible, the conditions pertaining within a severe reactor accident. Small segments of fuel were heated to ∼2000 K and the resulting vapour-aerosol release was studied along a pathway simulating the upper plenum, hot-leg structures and containment. (author)

  17. Stability and reproducibility of a single-sample urinary C-peptide/creatinine ratio and its correlation with 24-h urinary C-peptide.

    Science.gov (United States)

    McDonald, Tim J; Knight, Bridget A; Shields, Beverley M; Bowman, Pamela; Salzmann, Maurice B; Hattersley, Andrew T

    2009-11-01

    C-peptide measurement in blood or 24-h urine samples provides useful information regarding endogenous insulin secretion, but problems related to the rapid degradation of C-peptide in blood and difficulty of 24-h urine collection have limited widespread routine clinical use of this test. We assessed the feasibility of measuring urinary C-peptide (UCP) with correction for creatinine concentration in single urine samples. We analyzed UCP using a routine electrochemiluminescence immunoassay in samples from 21 healthy volunteers. We investigated the stability of UCP with different preservatives and storage conditions and compared the reproducibility of urinary C-peptide/creatinine ratio (UCPCR) in first- and second-void fasting urines, then assessed correlations with 24-h collections. UCPCR was unchanged at room temperature for 24 h and at 4 degrees C for 72 h even in the absence of preservative. UCPCR collected in boric acid was stable at room temperature for 72 h. UCPCR remained stable after 7 freeze-thaw cycles but decreased with freezer storage time and dropped to 82%-84% of baseline by 90 days at -20 degrees C. Second-void fasting UCPCRs were lower than first-void (median 0.78 vs 1.31, P = 0.0003) and showed less variation (CV 33% vs 52%), as second-void UCPCRs were not influenced by evening food-related insulin secretion. Second-void fasting UCPCR was highly correlated with 24-h UCP (r = 0.8, P = 0.00006). Second-void fasting UCPCR is a reproducible measure that correlates well with 24-h UCP in normal samples. The 3-day stability of UCPCR at room temperature greatly increases its potential clinical utility.

  18. Analytical methods for the determination of boron in reactor materials programme

    International Nuclear Information System (INIS)

    Chitre, R.S.; Joshi, V.R.; Iyer, C.S.P.

    1983-01-01

    Spectrophotometric methods of determination of boron based on the complexation reaction between boric acid and protonated curcumin are briefly reviewed. Direct determination of boron in heavy water, plant leaves, copper and its alloys, and aluminium and its alloys using a modified method of Hayes and Metcalfe is described. A method for determination of boron, when its content is very low as in case of uranium metal, diuranate, uranium oxide and thorium nitrate, is also described. In this method, boron is first separated as methyl borate by distillation of the sample with methanol in acid media. The distilled ester is absorbed by hydroxide solution and boron is analysed after removal of methanol. The precision obtained is indicated. (M.G.B.)

  19. Quantification of fatty acids as methyl esters and phospholipids in cheese samples after separation of triacylglycerides and phospholipids.

    Science.gov (United States)

    Hauff, Simone; Vetter, Walter

    2009-03-23

    Determination of the individual fatty acid composition of neutral- and phospholipids as well as the phospholipid content of dairy food and other foodstuffs are important tasks in life sciences. For these purposes, a method was developed for the separation of lipids (standards of triolein and diacylphosphatidylcholines as well as three cheese samples) by solid-phase extraction using a self-packed column filled with partly deactivated silica. Non-halogenated solvents were used for the elution of the lipid classes. Cyclohexane/ethyl acetate (1:1, v/v) served for the elution of neutral lipids, while polar lipids were eluted with three solvents (ethyl acetate/methanol, methanol, and methanol/water) into one fraction. The separated lipid fractions were transesterified and the individual fatty acids were quantified by using gas chromatography coupled to electron ionization mass spectrometry (GC/EI-MS) in the selected ion monitoring (SIM) mode. The recovery rate for standard phosphatidylcholines was approximately 90% and cross-contamination from neutral lipids was negligible. The method was applied to cheese samples. Quantitative amounts of individual fatty acids in the phospholipid fraction were camembert, cheese. Differences in the fatty acid pattern of neutral and polar lipids were detected. The quantity of the fatty acids determined in the phospholipid fraction was divided by the factor 0.7 in order to convert the fatty acid content into the phospholipid content of the cheese samples. This factor is based on the contribution of 16:0 to dipalmitoylphosphatidylcholine (DPPC). The resulting DPPC equivalents (DPPC(eq)) were found to be representative for the average contribution of fatty acids to all classes of phospholipids in dairy products. Using this approach, the phospholipid content of lipids from mozzarella, camembert, and goat cream cheese was 0.60%, 1.42% and 0.79%, respectively.

  20. Influence of water chemistry on IGSCC growth rate of SUS316 under high temperature water

    International Nuclear Information System (INIS)

    Fukumura, Takuya; Terachi, Takumi; Arioka, Koji

    2005-01-01

    The influence of the environment on intergranular stress corrosion crack behavior was examined by performing tensile tests in high-temperature water using cold-water non-sensitized 316 stainless steel. In the constant elongation test, the crack growth rate showed a clear environmental dependence on the concentration of dissolved hydrogen, boric acid and lithium, but no such environmental dependence was observed in the compact tension test. Regarding the influence of the environment on the intergranular stress corrosion crack behavior of non-sensitized 316 stainless steel, it is considered that the environmental factors of dissolved hydrogen (3-45 cc/kgH 2 O), boric acid (500-3500 ppm) and lithium (0.05-10 ppm) greatly affect the initiation process but do not significantly affect the propagation process. (author)

  1. Electrochemical measurements in PWR steam generators to follow crevice chemistry

    International Nuclear Information System (INIS)

    Feron, D.

    1991-01-01

    In PWR steam generator crevices, the evolution of chemistry is important for the understanding of corrosion phenomena. Electrochemical measurements have been performed in high temperature simulated crevice environments in order to follow hideout processes and remedial actions (on-line addition of boric acid). Reported tests have been conducted with model boilers of AJAX facilities. Eccentric and concentric tube support plate crevices have been instrumented with platinum electrodes. Electrochemical measurements have been collected when model boiler was under nominal conditions (primary temperature: 335 deg C, secondary temperature: 280 deg C). They include Electrochemical Impedance Spectroscopy (EIS) and potential measurements: with EIS, sodium and boric acid hideouts have been detected and followed. Potential measurements have been performed in an attempt to measure crevice PH evolution

  2. Prediction of Layer Thickness in Molten Borax Bath with Genetic Evolutionary Programming

    Science.gov (United States)

    Taylan, Fatih

    2011-04-01

    In this study, the vanadium carbide coating in molten borax bath process is modeled by evolutionary genetic programming (GEP) with bath composition (borax percentage, ferro vanadium (Fe-V) percentage, boric acid percentage), bath temperature, immersion time, and layer thickness data. Five inputs and one output data exist in the model. The percentage of borax, Fe-V, and boric acid, temperature, and immersion time parameters are used as input data and the layer thickness value is used as output data. For selected bath components, immersion time, and temperature variables, the layer thicknesses are derived from the mathematical expression. The results of the mathematical expressions are compared to that of experimental data; it is determined that the derived mathematical expression has an accuracy of 89%.

  3. Reproductive toxicity in boron exposed workers in Bandirma, Turkey.

    Science.gov (United States)

    Başaran, Nurşen; Duydu, Yalçin; Bolt, Hermann M

    2012-06-01

    Boric acid and sodium borates have been considered as being "toxic to reproduction and development", following results of animal studies with high doses. However unfavorable effects of boron exposure on reproduction and development have not been proved in epidemiological studies so far. The aim of the present study was to investigate the reproductive toxicity indicators in highly exposed workers employed in a boric acid production plant in Bandırma, Turkey. Two hundred and four workers participated in this study. The mean blood boron concentration of the high exposure group of workers was 223.89 ± 69.49 (152.82-454.02)ng/g. Unfavorable effects of boron exposure on the reproductive toxicity indicators were not observed. Copyright © 2012 Elsevier GmbH. All rights reserved.

  4. The effects of acid treatment and sample preparation on 40Ar/39Ar ages

    Science.gov (United States)

    Morgan, L. E.; Davidheiser, B.; Kuiper, K.; Wijbrans, J. R.

    2011-12-01

    Practitioners of K-Ar and 40Ar/39Ar geochronology regularly use dilute acids (typically 5-10% hydrofluoric acid (HF)) to clean mineral grains prior to irradiation (in the case of 40Ar/39Ar), and analysis (e.g. Evernden and Curtis, 1965; Dalrymple, 1967). This treatment has been shown to reduce contamination from atmospheric Ar, which consists largely of 40Ar and thus must be differentiated from radiogenic 40Ar* (Evernden and Curtis, 1965). Acid treatments can also remove fine grained material attached to mineral grains, such as glass shards or devitrified glass, which can affect analyses and is difficult to remove by other means (Evernden and Curtis, 1965). Such treatments were originally examined for their efficacy in reducing atmospheric argon contamination (Dalrymple, 1967) but were not assessed for the possibility of leaching Ar* or K differentially, which would affect both K-Ar and 40Ar/39Ar ages. Indeed, Evernden and Curtis (1965) state that they are simply removing the "outer portions of the crystals" and apparently do not account for the potential for leaching of 40Ar* or K from the mass of their host mineral. Moreover, the capabilities of the K-Ar system in the 1960s was limited to a precision of ca. 3-4% on samples of 1-3 Ma (Cox and Dalrymple, 1967). Effects of smaller magnitude could not have been detected at the time. As the developments of the 40Ar/39Ar system and modern mass spectrometer technology have allowed for precision to approach 0.1%, the potential effects of acid treatment during sample preparation warrant revisiting. Additionally, the use of Calgon for sample disintegration has not previously been quantitatively assessed but is used extensively in some laboratories. Here we present a series of experiments from co-irradiated Fish Canyon sanidine (FCs) and Mes-4 (Kuiper et al., 2008). FCs is used as the mineral standard following standard procedures. Mes-4 splits were treated with H2O (10 minutes, ultrasonic), Calgon (10%, overnight at 50

  5. Spectroscopic studies of humic acids from subsurface sediment samples collected across the Aegean Sea

    Directory of Open Access Journals (Sweden)

    F. SAKELLARIADOU

    2006-12-01

    Full Text Available Natural humic acids are biogenic, structurally complex and heterogeneous, refractory, acidic, yellow-to black-coloured organic polyelectrolytes of relatively high molecular weight. They occur in all soils, sediments, fresh waters, and seawaters. Humic acids represent the largest portion of nonliving soil organic matter. In the present paper, humic substances were isolated from marine subsurface sediment samples collected across the Aegean sea (in Greece and especially from a marine area extending northwards of the Samothraki plateau towards the north-eastern part of the island of Crete. In a following step, humic preparations were studied using infrared and fluorescence spectroscopy (emission, excitation and synchronous-scan excitation spectra were obtained. The infrared spectra suggested functional chemical groups such as as OH-, C-H aliphatic, C=C, C=O/COO-, salts of carboxylic acids, and also, in some cases, silicate anions or C-O from alcohols, esters and ethers. Fluorescence emission, excitation and synchronous scan excitation provided some valuable information concerning a probable origin (marine and/or terrestrial for the isolated humics.

  6. Effects of impregnation with boron compounds on the surface ...

    African Journals Online (AJOL)

    Liebl.) which met the requirements of ASTM D 358 were impregnated according to ASTM D 1413 with boric acid (Ba) and borax (Bx) by vacuum technique. After impregnation, surfaces were coated with cellulosic, synthetic, polyurathane, water-based, acrylic and acid hardening varnishes in accordance with ASTM D 3023 ...

  7. Thermal-hydraulic studies on the safety of VVER-440 type nuclear power plants

    International Nuclear Information System (INIS)

    Tuunanen, J.

    1994-01-01

    The thesis includes several thermal-hydraulic analyses related to the Loviisa VVER-440 nuclear power plant units. The work consists of experimental studies, analysis of the experiments, analysis of some plant transients and development of a calculational model for calculation of boric concentrations in the reactor. In the first part of thesis, in the case of simulation of boric acid solution behaviour during long-term cooling period of LOCAs, experiments were performed in scaled-down test facilities. The experimental data together with the results of RELAP5/MOD3 simulations were used to develop a model for calculations of boric acid concentrations in the reactor during LOCAs. In the second part, in the case of simulation of horizontal generators, experiments were performed with PACTEL integral test loop to simulate loss of feedwater transients. The PACTEL experiments as well as earlier REWETT-III natural circulation tests, were analyzed with RELAP5/MOD3 Version 5m5 code. The third part of the work consists of simulations of Loviisa VVER reactor pump trip transients with RELAP5/MOD1-Eur, RELAP5/MOD3 and CATHARE codes. (56 refs., 9 figs.)

  8. Theory of Ion and Water Transport in Reverse-Osmosis Membranes

    Science.gov (United States)

    Oren, Y. S.; Biesheuvel, P. M.

    2018-02-01

    We present a theory for ion and water transport through reverse-osmosis (RO) membranes based on a Maxwell-Stefan framework combined with hydrodynamic theory for the reduced motion of particles in thin pores. We take into account all driving forces and frictions both on the fluid (water) and on the ions including ion-fluid friction and ion-wall friction. By including the acid-base characteristic of the carbonic acid system, the boric acid system, H3O+/OH- , and the membrane charge, we locally determine p H , the effective charge of the membrane, and the dissociation degree of carbonic acid and boric acid. We present calculation results for an experiment with fixed feed concentration, where effluent composition is a self-consistent function of fluxes through the membrane. A comparison with experimental results from literature for fluid flow vs pressure, and for salt and boron rejection, shows that our theory agrees very well with the available data. Our model is based on realistic assumptions for the effective size of the ions and makes use of a typical pore size of a commercial RO membrane.

  9. Impact of reactor water chemistry on cladding performance

    Energy Technology Data Exchange (ETDEWEB)

    Cox, B. [University of Toronto, Centre for Nuclear Engineering, Toronto, Ontario (Canada)

    1997-07-01

    Water chemistry may have a major impact on fuel cladding performance in PWRs. If the saturation temperature on the surface of fuel cladding is exceeded, either because of the thermal hydraulics of the system, or because of crud deposition, then LiOH concentration can occur within thick porous oxide films on the cladding. This can degrade the protective film and accelerate the corrosion rate of the cladding. If sufficient boric acid is also present in the coolant then these effects may be mitigated. This is normally the case through most of any reactor fuel cycle. Extensive surface boiling may disrupt this equilibrium because of the volatility of boric acid in steam. Under such conditions severe cladding corrosion can ensue. The potential for such effects on high burnup cladding in CANDU reactors, where bone acid is not present in the primary coolant, is discussed. (author)

  10. Impact of reactor water chemistry on cladding performance

    International Nuclear Information System (INIS)

    Cox, B.

    1997-01-01

    Water chemistry may have a major impact on fuel cladding performance in PWRs. If the saturation temperature on the surface of fuel cladding is exceeded, either because of the thermal hydraulics of the system, or because of crud deposition, then LiOH concentration can occur within thick porous oxide films on the cladding. This can degrade the protective film and accelerate the corrosion rate of the cladding. If sufficient boric acid is also present in the coolant then these effects may be mitigated. This is normally the case through most of any reactor fuel cycle. Extensive surface boiling may disrupt this equilibrium because of the volatility of boric acid in steam. Under such conditions severe cladding corrosion can ensue. The potential for such effects on high burnup cladding in CANDU reactors, where bone acid is not present in the primary coolant, is discussed. (author)

  11. Fate and behavior of an organo-borate in the soil-plant system

    International Nuclear Information System (INIS)

    Adriano, D.C.; Mills, G.L.; Afre, J.L.; Hart, R.J.

    1984-01-01

    An organo-borate, sodium tetraphenylboron (NaTPB), is used to precipitate radiocesium in high level nuclear wastes in conjunction with the 'glassification' of these wastes for long-term storage. Because of the possibility of this compound interacting with the environment through land application of the waste supernate or ground burial of the waste 'saltblocks', studies were undertaken to evaluate the environmental chemistry of this compound. Results indicate that the parent compound, NaTPB, is unstable in the soil-plant system, yielding two primary degradation products, biphenyl and diphenylborinic acid. Plant growth and B uptake data further indicate that the growth of plants was more deleteriously affected by NaTPB soil treatment than by comparable soil treatment with boric acid, in spite of the much greater uptake of B from boric acid. This can be attributed to the hypothesized aggravating effect of biphenyl on plant growth. (author)

  12. A solid phase extraction procedure for the determination of Cd(II) and Pb(II) ions in food and water samples by flame atomic absorption spectrometry.

    Science.gov (United States)

    Daşbaşı, Teslima; Saçmacı, Şerife; Ülgen, Ahmet; Kartal, Şenol

    2015-05-01

    A relatively rapid, accurate and precise solid phase extraction method is presented for the determination of cadmium(II) and lead(II) in various food and water samples. Quantitation is carried out by flame atomic absorption spectrometry (FAAS). The method is based on the retention of the trace metal ions on Dowex Marathon C, a strong acid cation exchange resin. Some important parameters affecting the analytical performance of the method such as pH, flow rate and volume of the sample solution; type, concentration, volume, flow rate of the eluent; and matrix effects on the retention of the metal ions were investigated. Common coexisting ions did not interfere on the separation and determination of the analytes. The detection limits (3 σb) for Cd(II) and Pb(II) were found as 0.13 and 0.18 μg L(-1), respectively, while the limit of quantification values (10 σb) were computed as 0.43 and 0.60 μg L(-1) for the same sequence of the analytes. The precision (as relative standard deviation was lower than 4% at 5 μg L(-1) Cd(II) and 10 μg L(-1) Pb(II) levels, and the preconcentration factor was found to be 250. The accuracy of the proposed procedure was verified by analysing the certified reference materials, SPS-WW2 Batch 108 wastewater level 2 and INCT-TL-1 tea leaves, with the satisfactory results. In addition, for the accuracy of the method the recovery studies (⩾ 95%) were carried out. The method was applied to the determination of the analytes in the various natural waters (lake water, tap water, waste water with boric acid, waste water with H2SO4) and food samples (pomegranate flower, organic pear, radish leaf, lamb meat, etc.), and good results were obtained. While the food samples almost do not contain cadmium, they have included lead at low levels of 0.13-1.12 μg g(-1). Copyright © 2014 Elsevier Ltd. All rights reserved.

  13. WEED CONTROL AND BORON NUTRITION ON Eucalyptus IN SILVOPASTORAL SYSTEM

    Directory of Open Access Journals (Sweden)

    Alexandre Magno Brighenti

    2015-04-01

    Full Text Available The objective of this study was to evaluate the control of weeds in the rows of eucalyptus (Eucalyptus urograndis with herbicides applied singly or combined with boron (B, as well as, the response of Eucalyptus plants to this micronutrient. The experiments were carried out in a split-plot with randomized complete block design, with three replicates. Six treatments were applied to the plots: (i weeded control, (ii control without weeding, (iii glyphosate (1080 g ae ha-1 + chlorimuron-ethyl (10 g ai ha-1 + 0.05% v / v mineral oil, (iv glyphosate (1080 g ae  ha-1 + isoxaflutole (112.5 g ai ha-1,  (v glyphosate (1080 g ae ha-1 and  (vi oxyfluorfen (480 g ai ha-1. The sub-plots consisted of the absence or presence of 4 kg of boric acid (H3BO3 - 17% B in 100 L of water. The addition of boric acid in the solution containing the herbicides did not affect the weed control. There was an increase in boron content in the soil and consequently an increase in the boron levels in the eucalyptus leaves. The combined application of herbicides plus boric acid is perfectly suitable for preventing dry of the pointer on eucalyptus plants. Keywords: Eucalyptus urograndis; chemical control; herbicides; micronutrients; Urochloa decumbens.

  14. Determination of trace elements in biological samples treated with formic acid by inductively coupled plasma mass spectrometry using a microconcentric nebulizer

    International Nuclear Information System (INIS)

    Tormen, Luciano; Gil, Raul A.; Frescura, Vera L.A.; Dante Martinez, Luis; Curtius, Adilson J.

    2010-01-01

    A simple and fast method for the determination of As, Ba, Cd, Co, Cu, Fe, Ga, Mn, Mo, Ni, Pb, Rb, Se, Sr, Tl, U, V and Zn in biological samples by inductively coupled plasma mass spectrometry (ICP-MS), after sample solubilization with formic acid and introduction by a microconcentric nebulizer, is proposed. The sample is mixed with formic acid, kept at 90 o C for one hour and then diluted with nitric acid aqueous solution to a 50% v/v formic acid and 1% v/v nitric acid final concentrations. The final sample solution flow rate for introduction into the plasma was 30 μL min -1 . The optimized and adopted nebulizer gas flow rate was 0.7 L min -1 and RF power was 800 W. These conditions are very different than those normally used when a conventional nebulizer is employed. Rodhium was used as internal standard. External calibration against aqueous standard solutions, without formic acid, could be used for quantification, except for As, Se and Zn. However, external calibration with 50% formic acid allows the determination of all analytes with high accuracy and it is recommended. The detection limits were between 0.0005 (Tl) and 0.22 mg kg -1 (Fe) and the precision expressed by the relative standard deviations (RSD) were between 0.2% (Sr) and 3.5% (Ga). Accuracy was validated by the analysis of four certified reference biological materials of animal tissues, comparing the results by linear regressions and by the t-test at a 95% confidence level. The recommended procedure avoids plasma instability and carbon deposit on the cones.

  15. Effect of NaOH on large-volume sample stacking of haloacetic acids in capillary zone electrophoresis with a low-pH buffer.

    Science.gov (United States)

    Tu, Chuanhong; Zhu, Lingyan; Ang, Chay Hoon; Lee, Hian Kee

    2003-06-01

    Large-volume sample stacking (LVSS) is an effective on-capillary sample concentration method in capillary zone electrophoresis, which can be applied to the sample in a low-conductivity matrix. NaOH solution is commonly used to back-extract acidic compounds from organic solvent in sample pretreatment. The effect of NaOH as sample matrix on LVSS of haloacetic acids was investigated in this study. It was found that the presence of NaOH in sample did not compromise, but rather help the sample stacking performance if a low pH background electrolyte (BGE) was used. The sensitivity enhancement factor was higher than the case when sample was dissolved in pure water or diluted BGE. Compared with conventional injection (0.4% capillary volume), 97-120-fold sensitivity enhancement in terms of peak height was obtained without deterioration of separation with an injection amount equal to 20% of the capillary volume. This method was applied to determine haloacetic acids in tap water by combination with liquid-liquid extraction and back-extraction into NaOH solution. Limits of detection at sub-ppb levels were obtained for real samples with direct UV detection.

  16. X-ray fluorescence spectrometric and optical emission spectographic analysis of thoria in thoriated copper metal powder

    International Nuclear Information System (INIS)

    Chandola, L.C.; Khanna, P.P.

    1984-01-01

    Two methods, one using the X-ray fluorescence (XRF) spectrometric technique and another using optical emission spectrographic (OES) technique are described for the determination of thoria in the concentration range 0.5-10% in thoriated copper metal powder. The precision of XRF method is superior to OES method but when sample quantity is very small, the OES method is useful. For XRF method, 500 mg sample is mixed with boric acid binding material and converted to a tablet for analysis. For OES method, only 200 mg sample is needed which is glued to the flat ends of two graphite electrodes for excitation by AC arc. The precision obtained in XRF is better than +-1% and in OES it is +-23%. (author)

  17. Quantification of fatty acids as methyl esters and phospholipids in cheese samples after separation of triacylglycerides and phospholipids

    Energy Technology Data Exchange (ETDEWEB)

    Hauff, Simone [University of Hohenheim, Institute of Food Chemistry, Garbenstrasse 28, D-70599 Stuttgart (Germany); Vetter, Walter [University of Hohenheim, Institute of Food Chemistry, Garbenstrasse 28, D-70599 Stuttgart (Germany)], E-mail: w-vetter@uni-hohenheim.de

    2009-03-23

    Determination of the individual fatty acid composition of neutral- and phospholipids as well as the phospholipid content of dairy food and other foodstuffs are important tasks in life sciences. For these purposes, a method was developed for the separation of lipids (standards of triolein and diacylphosphatidylcholines as well as three cheese samples) by solid-phase extraction using a self-packed column filled with partly deactivated silica. Non-halogenated solvents were used for the elution of the lipid classes. Cyclohexane/ethyl acetate (1:1, v/v) served for the elution of neutral lipids, while polar lipids were eluted with three solvents (ethyl acetate/methanol, methanol, and methanol/water) into one fraction. The separated lipid fractions were transesterified and the individual fatty acids were quantified by using gas chromatography coupled to electron ionization mass spectrometry (GC/EI-MS) in the selected ion monitoring (SIM) mode. The recovery rate for standard phosphatidylcholines was {approx}90% and cross-contamination from neutral lipids was negligible. The method was applied to cheese samples. Quantitative amounts of individual fatty acids in the phospholipid fraction were <0.002-0.29% of total lipids from camembert, <0.002-0.12% of total lipids from mozzarella, and <0.002-0.18% of total lipids in a goat cream cheese. Differences in the fatty acid pattern of neutral and polar lipids were detected. The quantity of the fatty acids determined in the phospholipid fraction was divided by the factor 0.7 in order to convert the fatty acid content into the phospholipid content of the cheese samples. This factor is based on the contribution of 16:0 to dipalmitoylphosphatidylcholine (DPPC). The resulting DPPC equivalents (DPPC{sub eq}) were found to be representative for the average contribution of fatty acids to all classes of phospholipids in dairy products. Using this approach, the phospholipid content of lipids from mozzarella, camembert, and goat cream cheese

  18. Discriminative power of an assay for automated in vitro screening of teratogens

    DEFF Research Database (Denmark)

    Walmod, Peter S; Gravemann, Ute; Nau, Heinz

    2004-01-01

    -trans-retinoic acid, pentyl-4-yn-valproic acid, saccharin, salicylic acid and valproic acid. All compounds, with the exception of dimethadione inhibited proliferation in a linear dose-dependent manner, and there were statistically significant compound class-dependent differences between the IC(50)-values...... to teratogenicity were: 5-bromo-2(')-deoxyuridine, 6-aminonicotinamide, acrylamide, boric acid, D-(+)-camphor, dimethadione, dimethyl phthalate, diphenhydramine, hydroxyurea, isobutyl-ethyl-valproic acid, lithium chloride, methyl mercury chloride, methotrexate, methoxyacetic acid, penicillin G, all...

  19. Characterization of sulfur-oxidizing bacteria isolated from acid mine drainage and black shale samples

    International Nuclear Information System (INIS)

    Sajjad, W.; Bhatti, T. M.; Hasan, F.; Khan, S.; Badshah, M.

    2016-01-01

    Acid mine drainage (AMD) and black shale (BS) are the main habitats of sulfur-oxidizing bacteria. The aim of this study was to isolate and characterize sulfur-oxidizing bacteria from extreme acidic habitats (AMD and BS). Concentration of metals in samples from AMD and BS varied significantly from the reference samples and exceeded the acceptable limits set by the Environmental Protection Agency (EPA) and the World Health Organization (WHO). A total of 24 bacteria were isolated from these samples that were characterized both morphologically as well as through biochemical tests. All the bacteria were gram-negative rods that could efficiently oxidize sulfur into sulfate ions (SO/sub 4/-2), resulted into decrease in pH up to 1.0 when grown in thiosulfate medium with initial pH 4.0. Out of 24, only 06 isolates were selected for phylogenetic analysis through 16S rRNA sequencing, on the basis of maximum sulfur-oxidizing efficiency. The isolates were identified as the species from different genera such as Alcaligenes, Pseudomonas, Bordetella, and Stenotrophomonas on the basis of maximum similarity index. The concentration of sulfate ions produced was estimated in the range of 179-272 mg/L. These acidophiles might have various potential applications such as biological leaching of metals from low-grade ores, alkali soil reclamation and to minimize the use of chemical S-fertilizers and minimize environmental pollution. (author)

  20. Optimized Analytical Method to Determine Gallic and Picric Acids in Pyrotechnic Samples by Using HPLC/UV (Reverse Phase)

    International Nuclear Information System (INIS)

    Garcia Alonso, S.; Perez Pastor, R. M.

    2013-01-01

    A study on the optimization and development of a chromatographic method for the determination of gallic and picric acids in pyrotechnic samples is presented. In order to achieve this, both analytical conditions by HPLC with diode detection and extraction step of a selected sample were studied. (Author)

  1. Determination of Cd, Pb and As in sediments of the Sava River by electrothermal atomic absorption spectrometry

    Directory of Open Access Journals (Sweden)

    SIMONA MURKO

    2010-01-01

    Full Text Available The applicability of nitric acid, palladium nitrate and a mixture of palladium and magnesium nitrate as matrix modifiers were estimated for the accurate and reproducible determination of cadmium (Cd, lead (Pb and arsenic (As in sediments of the Sava River by electrothermal atomic absorption spectrometry, ETAAS. Decomposition of the samples was done in a closed vessel microwave-assisted digestion system using nitric, hydrochloric and hydrofluoric acids, followed by the addition of boric acid to convert the fluorides into soluble complexes. The parameters for the determination of Cd, Pb and As in sediments were optimised for each individual element and for each matrix modifier. In addition, two sediment reference materials were also analysed. In determination of Cd and Pb, nitric acid was found to be the most appropriate matrix modifier. The accurate and reliable determination of Cd and Pb in sediments was possible also in the presence of boric acid. The use of a mixture of palladium and magnesium nitrate efficiently compensated for matrix effects and enabled the accurate and reliable determination of As in the sediments. Quantification of Cd and As was performed by calibration using acid matched standard solutions, while the standard addition method was applied for the quantification of Pb. The repeatability of the analytical procedure for the determination of Cd, Pb and As in sediments was ±5 % for Cd, ±4 % for Pb and ±2 % for As. The LOD values of the analytical procedure were found to be 0.05 mg/kg for Cd and 0.25 mg/kg for Pb and As, while the LOQ values were 0.16 mg/kg for Cd and 0.83 mg/kg for Pb and As. Finally, Cd, Pb and As were successfully determined in sediments of the Sava River in Slovenia.

  2. Development and evaluation of polyethylene as solidification agent for low-level waste

    International Nuclear Information System (INIS)

    Franz, E.M.; Colombo, P.

    1986-09-01

    A polyethylene solidification process, using an extrusion system, has been developed for the immobilization of dry wastes resulting from volume reduction technologies. Ease of processibility and high packing efficiencies were obtained through the use of low-density polyethylene (0.917 to 0.924 g/cm 3 ) with melt indices from 2.0 to 55.0 g/10 min. Maximum waste loadings of 70 wt % sodium sulfate, 50 wt % boric acid, 40 wt % incinerator ash and 65 wt % ion exchnge were obtained. A series of tsts were conducted to assess the acceptability of polyethylene waste forms to meet the requirements of 10 CFR 61. Based on test results and process control considerations, optimal waste loadings of 70 wt % sodium sulfate, 50 wt % boric acid, 40 wt % incinerator ash and 30 wt % ion exchange resins are recommended

  3. Material and water chemistry for a ferritic reactor coolant system in pressure water reactors

    International Nuclear Information System (INIS)

    Stieding, L.

    1979-04-01

    The use of unplated, low-alloy steels in a boric acid controlled PWR is not considered possible without changing the water conditions during the start-up and shut-down periods of the reactor. The significant pH reduction of the water due to boric acid during these periods most probably leads to damage of the magnetite protective layers followed by selective corrosion. As this highly important process has not been sufficiently evaluated with respect to our specific application problem, more detailed information will be necessary. KWU test facilities provide a means of performing such tests. In order to avoid corrosion attack during the above operating conditions, an inhibition of the water with 7 Li-borate is recommended which, however, will amount to approx. DM 60.000,-- per period of use. (orig.) [de

  4. Effects of Treatment Materials on the Physical Properties of Eucalyptus (Eucalyptus camaldulensis Dehn. Wood

    Directory of Open Access Journals (Sweden)

    Selahattin Bardak

    2011-04-01

    Full Text Available This study was designed to determine effects on retention and shrink levels of Eucalyptus (Eucalyptus camaldulensis Dehn. which treated with some commercial preservative types, borates, polyethylene glycol, and water repellents. In this study, four type impregnation chemicals were chosen: 1. Commercial preservative types, [Ammonium sulphate, Vacsol-WR WR and Immersol-WR (WR], 2. Borates chemicals, [Boric acid, Borax, Boric acid+ Borax] 3. Polyethylene glycol such as Polyethylene glycol (PEG-400 4. Water repellents [Styrene, Methylmetacrylate.]. As a result, retention % and shrink levels of Eucalyptus wood was lower treated with commercial preservative types and borates preservatives compare to other treatment chemicals. However, retention % levels of Eucalyptus wood treated with WR chemicals were highly significant levels. According to their leachability period although PEG 400 showed antishrink effectiveness other treatments didnt showed antishrink efficiency.

  5. Studies of light water lattices by the homogeneous boron poisoning technique

    International Nuclear Information System (INIS)

    Bailly, J.; Calament, J.; Girard, Y.; Golinelli, C.

    1964-01-01

    By homogeneously poisoning a critical facility with boric acid, one can balance important reactivities. Furthermore this technique is particularly interesting, due to the fact that it allows the substitution of cross sections to kinetic parameters in lattice calculations. With this use of boric acid as a poison arise important technological problems which are described in this report, the last part of which deals with the accuracy of the measurements made in these conditions. The main features of a lattice study made according to this moderator poisoning technique concern the determination of the concentration of dissolved boron which makes the multiplying assembly just critical and the determination of the reactivity factor as a function of temperature (this study has been carried out fill above 95 deg. C). (authors) [fr

  6. Liquid chromatography-tandem mass spectrometry analysis of perfluorooctane sulfonate and perfluorooctanoic Acid in fish fillet samples.

    Science.gov (United States)

    Paiano, Viviana; Fattore, Elena; Carrà, Andrea; Generoso, Caterina; Fanelli, Roberto; Bagnati, Renzo

    2012-01-01

    Perfluorooctane sulfonate (PFOS) and perfluorooctanoic (PFOA) acid are persistent contaminants which can be found in environmental and biological samples. A new and fast analytical method is described here for the analysis of these compounds in the edible part of fish samples. The method uses a simple liquid extraction by sonication, followed by a direct determination using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The linearity of the instrumental response was good, with average regression coefficients of 0.9971 and 0.9979 for PFOS and PFOA, respectively, and the coefficients of variation (CV) of the method ranged from 8% to 20%. Limits of detection (LOD) were 0.04 ng/g for both the analytes and recoveries were 90% for PFOS and 76% for PFOA. The method was applied to samples of homogenized fillets of wild and farmed fish from the Mediterranean Sea. Most of the samples showed little or no contamination by perfluorooctane sulfonate and perfluorooctanoic acid, and the highest concentrations detected among the fish species analyzed were, respectively, 5.96 ng/g and 1.89 ng/g. The developed analytical methodology can be used as a tool to monitor and to assess human exposure to perfluorinated compounds through sea food consumption.

  7. Liquid Chromatography-Tandem Mass Spectrometry Analysis of Perfluorooctane Sulfonate and Perfluorooctanoic Acid in Fish Fillet Samples

    Directory of Open Access Journals (Sweden)

    Viviana Paiano

    2012-01-01

    Full Text Available Perfluorooctane sulfonate (PFOS and perfluorooctanoic (PFOA acid are persistent contaminants which can be found in environmental and biological samples. A new and fast analytical method is described here for the analysis of these compounds in the edible part of fish samples. The method uses a simple liquid extraction by sonication, followed by a direct determination using liquid chromatography-tandem mass spectrometry (LC-MS/MS. The linearity of the instrumental response was good, with average regression coefficients of 0.9971 and 0.9979 for PFOS and PFOA, respectively, and the coefficients of variation (CV of the method ranged from 8% to 20%. Limits of detection (LOD were 0.04 ng/g for both the analytes and recoveries were 90% for PFOS and 76% for PFOA. The method was applied to samples of homogenized fillets of wild and farmed fish from the Mediterranean Sea. Most of the samples showed little or no contamination by perfluorooctane sulfonate and perfluorooctanoic acid, and the highest concentrations detected among the fish species analyzed were, respectively, 5.96 ng/g and 1.89 ng/g. The developed analytical methodology can be used as a tool to monitor and to assess human exposure to perfluorinated compounds through sea food consumption.

  8. Determination of /sup 35/S-aminoacyl-transfer ribonucleic acid specific radioactivity in small tissue samples

    Energy Technology Data Exchange (ETDEWEB)

    Samarel, A.M.; Ogunro, E.A.; Ferguson, A.G.; Lesch, M.

    1981-11-15

    Rate determination of protein synthesis utilizing tracer amino acid incorporation requires accurate assessment of the specific radioactivity of the labeled precursor aminoacyl-tRNA pool. Previously published methods presumably useful for the measurement of any aminoacyl-tRNA were unsuccessful when applied to (/sup 35/S)methionine, due to the unique chemical properties of this amino acid. Herein we describe modifications of these methods necessary for the measurement of /sup 35/S-aminoacyl-tRNA specific radioactivity from small tissue samples incubated in the presence of (/sup 35/S)methionine. The use of (/sup 35/S)methionine of high specific radioactivity enables analysis of the methionyl-tRNA from less than 100 mg of tissue. Conditions for optimal recovery of /sup 35/S-labeled dansyl-amino acid derivatives are presented and possible applications of this method are discussed.

  9. Validation of a One-Step Method for Extracting Fatty Acids from Salmon, Chicken and Beef Samples.

    Science.gov (United States)

    Zhang, Zhichao; Richardson, Christine E; Hennebelle, Marie; Taha, Ameer Y

    2017-10-01

    Fatty acid extraction methods are time-consuming and expensive because they involve multiple steps and copious amounts of extraction solvents. In an effort to streamline the fatty acid extraction process, this study compared the standard Folch lipid extraction method to a one-step method involving a column that selectively elutes the lipid phase. The methods were tested on raw beef, salmon, and chicken. Compared to the standard Folch method, the one-step extraction process generally yielded statistically insignificant differences in chicken and salmon fatty acid concentrations, percent composition and weight percent. Initial testing showed that beef stearic, oleic and total fatty acid concentrations were significantly lower by 9-11% with the one-step method as compared to the Folch method, but retesting on a different batch of samples showed a significant 4-8% increase in several omega-3 and omega-6 fatty acid concentrations with the one-step method relative to the Folch. Overall, the findings reflect the utility of a one-step extraction method for routine and rapid monitoring of fatty acids in chicken and salmon. Inconsistencies in beef concentrations, although minor (within 11%), may be due to matrix effects. A one-step fatty acid extraction method has broad applications for rapidly and routinely monitoring fatty acids in the food supply and formulating controlled dietary interventions. © 2017 Institute of Food Technologists®.

  10. The impact of the MCU life extension solvent on sludge batch 8 projected operating windows

    International Nuclear Information System (INIS)

    Peeler, D.K.; Edwards, T.B.

    2013-01-01

    As a part of the Actinide Removal Process (ARP)/Modular Caustic Side Solvent Extraction Unit (MCU) Life Extension Project, a next generation solvent (NGS) and a new strip acid will be deployed. The strip acid will be changed from dilute nitric acid to dilute boric acid (0.01 M). Because of these changes, experimental testing or evaluations with the next generation solvent are required to determine the impact of these changes (if any) to Chemical Process Cell (CPC) activities, glass formulation strategies, and melter operations at the Defense Waste Processing Facility (DWPF). The introduction of the dilute (0.01 M) boric acid stream into the DWPF flowsheet has a potential impact on glass formulation and frit development efforts since B203 is a major oxide in frits developed for DWPF. Prior knowledge of this stream can be accounted for during frit development efforts but that was not the case for Sludge Batch 8 (SB8). Frit 803 has already been recommended and procured for SB8 processing; altering the frit to account for the incoming boron from the strip effluent (SE) is not an option for SB8. Therefore, the operational robustness of Frit 803 to the introduction of SE including its compositional tolerances (i.e., up to 0.0125M boric acid) is of interest and was the focus of this study. The primary question to be addressed in the current study was: What is the impact (if any) on the projected operating windows for the Frit 803 - SB8 flowsheet to additions of B203 from the SE in the Sludge Receipt and Adjustment Tank (SRAT)? More specifically, will Frit 803 be robust to the potential compositional changes occurring in the SRAT due to sludge variation, varying additions of ARP and/or the introduction of SE by providing access to waste loadings (WLs) of interest to DWPF? The Measurement Acceptability Region (MAR) results indicate there is very little, if any, impact on the projected operating windows for the Frit 803 - SB8 system regardless of the presence or absence of

  11. Determination of boron in waters by using methyl borate generation and flame atomic-emission spectrometry

    International Nuclear Information System (INIS)

    Castillo, J.R.; Mir, J.M.; Martinez, C.; Bendicho, C.

    1985-01-01

    An improved method is proposed for the determination of boron in waters. The esterification reaction between boric acid and methanol in a concentrated sulphuric acid medium and the vaporisation of the methyl borate formed (boiling-point, 68 C) are used in the determination by boron by measuring the emission of the BO 2 radical at 548 nm. This reaction is carried out in a simple and inexpensive generator, designed for this purpose, and the heat developed in it causes the rapid volatilisation of the methyl borate. Thus no collection systems or carrier gas are required. The proposed method gives an improved detection limit and it can be applied to the determination of boron in water samples. It is both rapid and highly selective. (author)

  12. Direct determination of mercury in cosmetic samples by isotope dilution inductively coupled plasma mass spectrometry after dissolution with formic acid

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Ying; Shi, Zeming; Zong, Qinxia; Wu, Peng; Su, Jing [Sichuan Provincial Key Laboratory of Nuclear Technology in Geology, College of Nuclear Technology and Automation Engineering, Chengdu University of Technology, Chengdu 610059 (China); Liu, Rui, E-mail: liur.ray@gmail.com [Mineral Resources Chemistry Key Laboratory of Sichuan Higher Education Institutions, College of Materials and Chemistry and Chemical Engineering, Chengdu University of Technology, Chengdu 610059 (China)

    2014-02-17

    Graphical abstract: -- Highlights: •Simple, sensitive, and accurate method is established for mercury determination in cosmetics. •The sample preparation procedure is highly simplified. •Isotope dilution efficiently eliminates matrix effect. •First report of using formic acid based method in combination with PVG-ID-ICP MS for mercury quantitation in cosmetics. -- Abstract: A new method was proposed for the accurate determination of mercury in cosmetic samples based on isotopic dilution (ID)-photochemical vapor generation (PVG)-inductively coupled plasma mass spectrometry (ICP MS) measurement. Cosmetic samples were directly dissolved in formic acid solution and subsequently subjected to PVG for the reduction of mercury into vapor species following by ICP MS detection. Therefore, the risks of analyte contamination and loss were avoided. Highly enriched {sup 201}Hg isotopic spike is added to cosmetics and the isotope ratios of {sup 201}Hg/{sup 202}Hg were measured for the quantitation of mercury. With ID calibration, the influences originating from sample matrixes for the determination of mercury in cosmetic samples have been efficiently eliminated. The effects of several experimental parameters, such as the concentration of the formic acid, and the flow rates of carrier gas and sample were investigated. The method provided good reproducibility and the detection limits were found to be 0.6 pg mL{sup −1}. Finally, the developed method was successfully applied for the determination of mercury in six cosmetic samples and a spike test was performed to verify the accuracy of the method.

  13. Field Sampling Plan for the HWMA/RCRA Closure Certification of the TRA-731 Caustic and Acid Storage Tank System - 1997 Notice of Violation Consent Order

    International Nuclear Information System (INIS)

    Evans, S.K.

    2002-01-01

    This Field Sampling Plan for the HWMA/RCRA Closure Certification of the TRA-731 Caustic and Acid Storage Tank System is one of two documents that comprise the Sampling and Analysis Plan for the HWMA/RCRA closure certification of the TRA-731 caustic and acid storage tank system at the Idaho National Engineering and Environmental Laboratory. This plan, which provides information about sampling design, required analyses, and sample collection and handling procedures, is to be used in conjunction with the Quality Assurance Project Plan for the HWMA/RCRA Closure Certification of the TRA-731 Caustic and Acid Storage Tank System

  14. Boron evaporation in thermally-driven seawater desalination: Effect of temperature and operating conditions.

    Science.gov (United States)

    Alpatova, A; Alsaadi, A; Ghaffour, N

    2018-06-05

    The volatilization of boron in thermal desalination processes, namely multi-stage flash (MSF) and air-gap membrane distillation (AGMD) was investigated for the first time. This phenomenon was observed at feed temperatures above 55 °C in both studied processes. In simulated MSF process with two feeds, model boric acid and Red Sea water, boron concentration in distillate increased with feed temperature increase from 55 °C to 104 °C because of the increase in boric acid vapor pressure. Salinity and pH were the main factors controlling boron evaporation. The achieved boron concentrations in simulated MSF process were consistent with those measured in distillate samples collected from commercial MSF plants. The AGMD process also revealed a strong influence of operating temperature on boron removal. However, unlike MSF process, the boron concentration in AGMD permeate decreased with the feed temperature increase from 55 °C to 80 °C due probably to increase in vapor production and corresponding permeate dilution. When AGMD was operated in concentrating mode at a constant feed temperature of 80 °C, permeate boron concentration increased with process time due to concentration polarization and membrane fouling. A 10% flux decline observed after 21 h was attributed to CaCO 3 scaling on the membrane surface. Copyright © 2018 Elsevier B.V. All rights reserved.

  15. Evaluation of tecniques for controlling UF6 release clouds in the GAT environmental chamber

    International Nuclear Information System (INIS)

    Lux, C.J.

    1982-01-01

    Studies designed to characterize the reaction between UF 6 and atmospheric moisture, evaluate environmental variables of UF 6 cloud formation and ultimate cloud fate, and UF 6 release cloud control procedure have been conducted in the 1200 cu. ft. GAT environmental chamber. In earlier chamber experiments, 30 separate UF 6 release tests indicated that variations of atmospheric conditions and sample sizes had no significant effect on UO 2 F 2 particle size distribution, release cloud formation, or cloud settling rates. During the past year, numerous procedures have been evaluated for accelerating UF 6 cloud knockdown in a series of 37 environmental chamber releases. Knockdown procedures included: coarse water spray; air jet; steam spray (electrostatically charged and uncharged); carbon dioxide; Freon-12; fine water mist (uncharged); boric acid mist (charged and uncharged); and an ionized dry air stream. UF 6 hydrolysis cloud settling rates monitored by a laser/powermeter densitometer, indicated the relative effectiveness of various cloud knockdown techniques. Electrostatically charged boric acid/water mist, and electrostatically ionized dry air were both found to be very effective, knocking down the UO 2 F 2 release cloud particles in two to five minutes. Work to adapt these knockdown techniques for use under field conditions is continuing, taking into account recovery of the released uranium as well as nuclear criticality constraints

  16. Linear titration plot for the determination of boron in the primary coolant of a pressurized water reactor

    International Nuclear Information System (INIS)

    Midgley, D.; Gatford, C.

    1992-01-01

    A linear titration plot method has been devised for the determination of boron as boric acid in partly neutralized solution, such as occurs in the primary coolant of pressurized water reactors. The total boron and the alkali in the sample are determined simultaneously. Although it is not essential to add mannitol in this method, it is more accurate when the solution is saturated with mannitol. Comparisons are made with other modes of titration: Gran plots, first and second differential potentiometric titrations and indicator titrations. None of these gives the total boron directly in partly neutralized solutions. (author)

  17. Contributions te the study of methods and factors affecting the spectrophotometric determination of boron traces with carmin uranium compounds

    International Nuclear Information System (INIS)

    Fernandez Cellini, R.; Gasco Sanchez, L.

    1956-01-01

    The study of some factors affecting the spectrophotometric determination of boron traces with carmin is made; the influence of carmin from different origin, the stability of complex carmin-boric acid in relation with the sulphuric acid concentration, the interference produced by ion nitrate, and the ion uraline and light influence are discussed. (Author) 36 refs

  18. Contributions te the study of methods and factors affecting the spectrophotometric determination of boron traces with carmin uranium compounds; Contribucion al estudio del metodo y factores que afectan a la determinacion espectrofotometrica de trazas de boro con Carmin en compuestos de uranio

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez Cellini, R; Gasco Sanchez, L

    1956-07-01

    The study of some factors affecting the spectrophotometric determination of boron traces with carmin is made; the influence of carmin from different origin, the stability of complex carmin-boric acid in relation with the sulphuric acid concentration, the interference produced by ion nitrate, and the ion uraline and light influence are discussed. (Author) 36 refs.

  19. Download this PDF file

    African Journals Online (AJOL)

    made visible by ethidium bromide. The results from gel electrophoresis were visualized on a UV transillumination. (254 nm). Agarose gel preparation as well as electrophoresis were carried out using buffer solution (pH 8.0), contain- ing 45 mmol/L Tris-base/boric acid and. 1 mmol/L EDTA adjusted with hydro- chloric acid.

  20. Cobalt (II)–EDTA complex as a new reductant for phosphomolybdic ...

    Indian Academy of Sciences (India)

    Unknown

    Trazodone; phosphomolybdic acid; cobalt nitrate; ethylenediamine tetra ... Aliquots of standard TZ solution (0⋅5–2⋅5 ml, 200 µg/ml in 0⋅01 M HCl) were ... 750 nm; εmax, 5⋅39 × 103 l mol–1 cm–1) was obtained after one hour if the reaction mixture ... starch (150-fold), boric acid (150-fold), stearic acid (70-fold), magnesium ...

  1. Personal monitors for inorganic gases. Final report, 28 September 1978-31 August 1979

    Energy Technology Data Exchange (ETDEWEB)

    West, P.W.

    1979-01-01

    Successful passive sampling techniques were developed for ammonia and hydrogen-cyanide. For ammonia the collection of the sample required permeation through a silicone membrane into boric acid. Spectrophotometric determination of the ammonia was carried out using Nessler's reagent or potentiometrical means with an ion-selective electrode. Linearity was demonstrated using the monitor over concentration ranges of less than 10 to over 160 parts per million. The ammonia monitor was relatively free from interference by amines and could be used in a badge-type monitor, as it was very light in weight and compact. The hydrogen-cyanide monitor functioned by permeation through a silicone membrane. The permeated gas was stabilized in sodium hydroxide and determined by means of a standard pyridine/barbituric acid colorimetric method. A detection limit of 10 parts per billion for an 8-hour exposure was obtained. Difficulties were encountered in developing a sampler for hydrogen sulfide.

  2. Extraction of nucleic acids from yeast cells and plant tissues using ethanol as medium for sample preservation and cell disruption.

    Science.gov (United States)

    Linke, Bettina; Schröder, Kersten; Arter, Juliane; Gasperazzo, Tatiana; Woehlecke, Holger; Ehwald, Rudolf

    2010-09-01

    Here we report that dehydrated ethanol is an excellent medium for both in situ preservation of nucleic acids and cell disruption of plant and yeast cells. Cell disruption was strongly facilitated by prior dehydration of the ethanol using dehydrated zeolite. Following removal of ethanol, nucleic acids were extracted from the homogenate pellet using denaturing buffers. The method provided DNA and RNA of high yield and integrity. Whereas cell wall disruption was essential for extraction of DNA and large RNA molecules, smaller molecules such as tRNAs could be selectively extracted from undisrupted, ethanol-treated yeast cells. Our results demonstrate the utility of absolute ethanol for sample fixation, cell membrane and cell wall disruption, as well as preservation of nucleic acids during sample storage.

  3. Modification of ntezi bentonite structure by hydrochloric acid: process kinetics and structural properties of the modified samples

    International Nuclear Information System (INIS)

    Ajemba, R.O.

    2014-01-01

    Bentonite from Ntezi was modified by reacting it with different concentrations of hydrochloric acid solutions. The modified samples were analysed by x-ray fluorescence. The kinetics of the modification reaction was studied by performing the experiment at different temperatures and times. Results of the analysis of the modified samples showed that the octahedral cations were removed which altered the chemical composition of the bentonite. The surface area and adsorptive capacity of the bentonite were improved after the modification. The kinetic studies showed that the acid modification reaction is controlled by the product layer diffusion and can be represented by (1-(l-X)/sup 1/3)/sup 2/ = k t; where, X is the fraction of the bentonite dissolved at time t. The activation energy was determined to be 24.98 kJ/mol. (author)

  4. Canada - Atomic Energy Control Board, Canada. Summary of a common cause failure event which occurred in a Canadian utility. 'Failure to Verify Poison Isotopic'

    International Nuclear Information System (INIS)

    1996-01-01

    Operating Policies and Principles (OP and Ps) are referenced in the reactor operating license. They contain not only general safety principles, but also define safety parameters and their numerical values for the operation of the nuclear power plant. The event described highlights the difficulties to implement the OP and Ps into detailed purchase orders. In Candu reactors gadolinium nitrate and boric oxide are used as neutron absorbers in the moderator. The concentration of neutron absorbers in the moderator is safety significant because a small change in concentration in coincidence with other failures (e.g. LOCA) can result in a sudden increase of power. To ensure that new shipments of gadolinium nitrate or boric acid meet the required specifications, these must undergo quarantine so that samples could be taken and forwarded for analysis. The chemistry unit of the NPP issued this requirements in a 'note to file'. In the event, two separated purchase orders, one for gadolinium nitrate and one for boric oxide, were placed. The purchase orders did not stipulate the requirements to quarantine, inform the chemistry unit or to analyse samples. They only stated that correct isotopic and chemical purity were required. The gadolinium nitrate as well as the boron oxide were both not quarantined and even the purity was not verified. The chemistry unit felt that a 'note to file' memo was sufficient to ensure that the OP and Ps are met taking into account the low shipment rate and sufficient experiences before. The analysis of the event revealed several causal factors. Four main factors were pointed out: - Work practices, - Resource Management, - Written communication, - Managerial methods. The actions taken after the event focused on the identified deficiencies

  5. Division of waste management programs. Progress report, July--December 1977

    International Nuclear Information System (INIS)

    Lerch, R.E.; Allen, C.R.

    1978-07-01

    An acid fractionator and acid recycle equipment were added to the Radioactive Acid Digestion Test Unit (RADTU). The first simulated waste was processed through RADTU in November. By the end of December RADTU had been operated up to its design capacity of 4 kg of waste/hour without major problems. The unit was operated for 23 hours and processed 62 kg of waste during initial shakedown testing. Borosilicate glass specimens, containing up to 33 wt percent acid digestion residue, were made after the sulfur was removed. The glass had a density of 2.6 g/cm 3 and produced a two-fold decrease in residue volume. During tests on the solubility of thorium oxide in the acid digestion system, thorium oxide was converted to a form, presumably thorium sulfate, that was soluble in either dilute nitric acid or water. Thorium sulfate has approximately the same solubility in acid digestion as plutonium, about 0.1 g/l, and strontium from the boric acid-cement samples were found to be excessively high during 14-day leach tests. Leach rates of cesium and strontium from the sodium sulfate-cement samples were much lower. Leach rate tests were also performed on mercuric iodate immobilized in cement. 12 figs., 10 tables

  6. Validation of a multi-analyte HPLC-DAD method for determination of uric acid, creatinine, homovanillic acid, niacinamide, hippuric acid, indole-3-acetic acid and 2-methylhippuric acid in human urine.

    Science.gov (United States)

    Remane, Daniela; Grunwald, Soeren; Hoeke, Henrike; Mueller, Andrea; Roeder, Stefan; von Bergen, Martin; Wissenbach, Dirk K

    2015-08-15

    During the last decades exposure sciences and epidemiological studies attracts more attention to unravel the mechanisms for the development of chronic diseases. According to this an existing HPLC-DAD method for determination of creatinine in urine samples was expended for seven analytes and validated. Creatinine, uric acid, homovanillic acid, niacinamide, hippuric acid, indole-3-acetic acid, and 2-methylhippuric acid were separated by gradient elution (formate buffer/methanol) using an Eclipse Plus C18 Rapid Resolution column (4.6mm×100mm). No interfering signals were detected in mobile phase. After injection of blank urine samples signals for the endogenous compounds but no interferences were detected. All analytes were linear in the selected calibration range and a non weighted calibration model was chosen. Bias, intra-day and inter-day precision for all analytes were below 20% for quality control (QC) low and below 10% for QC medium and high. The limits of quantification in mobile phase were in line with reported reference values but had to be adjusted in urine for homovanillic acid (45mg/L), niacinamide 58.5(mg/L), and indole-3-acetic acid (63mg/L). Comparison of creatinine data obtained by the existing method with those of the developed method showing differences from -120mg/L to +110mg/L with a mean of differences of 29.0mg/L for 50 authentic urine samples. Analyzing 50 authentic urine samples, uric acid, creatinine, hippuric acid, and 2-methylhippuric acid were detected in (nearly) all samples. However, homovanillic acid was detected in 40%, niacinamide in 4% and indole-3-acetic acid was never detected within the selected samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  7. Operational Environmental Assessment

    Science.gov (United States)

    1988-09-01

    Anhydride 0 oz Cupric Sulfide 5 lb Oxalic Acid 56 oz Potassium Carbonate Anhydrous 32 oz Potassium Phosphate 36 oz Sodium Acetate 44 oz Sodium...Benzene 35,500 ml Antimony Potassium Tartrate 4,000 gm Barbituric Acid 150 gm Barbituric Acid 400 gm Chromium Trioxide 6,000 gm Disodium Ethylenediamine...Hydrocholoride 600 gm *Benzene a pt Boric Acid 5,000 gm Calcium Chloride 6,500 gm Calcium Chloride 3 lb Citric Acid 3 lb Citric Acid 2,500 gm Cupric Sulfate 2,500

  8. IGA/SCC propagation rate measurements on alloy 600 steam generator tubing using a side stream model boiler

    International Nuclear Information System (INIS)

    Takamatsu, H.; Matsueda, K.; Matsunaga, T.; Kitera, T.; Arioka, K.; Tsuruta, T.; Okamoto, S.

    1993-01-01

    IGA/SCC crack propagation rate measurements using various types of IGA/SCC predefected ALloy 600 tubing were tested in model boilers, a side stream model boiler at Ohi Unit 1 and similar model boilers in the laboratory. Types of IGA/SCC predefects introduced from the outside of the tubing were as follows. (1) Actual IGA/SCC predefect introduced by high temperature caustic environments; (2) Longitudinal predefect by electrodischarge machining (EDM) method, and then crack tip fatigue was introduced to serve as the marker on the fractured surface (EDM slit + fatigue). IGA/SCC crack propagation rate was measured after the destructive examination by Cr concentration profile on fracture surface for (1), and observation of intergranular fractured surface propagated from the marked fatigue was employed for (2) and (3) after the model boiler tests. As for the water chemistry conditions, mainly AVT (high N 2 H 4 ) + boric acid (5-10ppm as B in SGs) treatment for both model boilers, and some of the tests for the model boiler in the laboratory employed AVT (high N 2 H 4 ) without boric acid. The results of IGA/SCC crack propagation rate measurements were compared with each other, and the three methods employed showed a good coincidence with the rate of ca. 1 x 10 -5 mm/Hr for AVT (high N 2 H 4 ) + boric acid treatment condition, in the case that crack tip boron intensity (B/O value by IMMA analysis) of more than 1 was observed

  9. In Vitro Pollen Germination of Eichhornia crassipes (Mart. Solms: An Insight into its Preferred Mode of Clonal Reproduction

    Directory of Open Access Journals (Sweden)

    Somnath BHOWMIK

    2012-05-01

    Full Text Available Eichhornia crassipes (Mart. Solms is an aquatic invasive weed throughout the tropical and subtropical regions of the world. The plant rarely produces any fruit under natural condition In order to understand the causes of failure of seed set in this plant various aspect of pollen biology were studied. Pollen fertility and pollen viability was assessed using Muntzing� s mixture and in acetic orcein and TTZ, while pollen germination was assessed with different concentrations of sucrose supplemented with boric acid and Ca and Mg salts. The aim of present study was to find out the cause of sexual incompatibility of Eichhornia crassipes (Mart. Solms. In spite of high pollen fertility, pollen viability and pollen germination the species show hardly any fruit set under natural condition. The abnormal pollen germination like curling of pollen tubes, shrinkage of pollen tube tips and bending of pollen tube might be reasons of sexual incompatibility of this species. It is observed that the taxa required comparatively low sucrose concentration (5% for their optimal in vitro pollen germination (54.08%. Boric acid to certain extent also influences the in vitro pollen germination (56.2%. In the present investigation the nature of substrate in association with the effect of Boric acid, CaCO3, MgSO4 on the in vitro pollen germination of Eichhornia crassipes is also worked out. However the tested salts show no significant effect on pollen germination in the present study.

  10. Retrospective bioindication of stratospheric ozone and ultraviolet radiation using hydroxycinnamic acid derivatives of herbarium samples of an aquatic liverwort

    Energy Technology Data Exchange (ETDEWEB)

    Otero, Saul [Universidad de La Rioja, Complejo Cientifico-Tecnologico, Avda. Madre de Dios 51, 26006 Logrono (La Rioja) (Spain); Nunez-Olivera, Encarnacion, E-mail: encarnacion.nunez@unirioja.e [Universidad de La Rioja, Complejo Cientifico-Tecnologico, Avda. Madre de Dios 51, 26006 Logrono (La Rioja) (Spain); Martinez-Abaigar, Javier; Tomas, Rafael [Universidad de La Rioja, Complejo Cientifico-Tecnologico, Avda. Madre de Dios 51, 26006 Logrono (La Rioja) (Spain); Huttunen, Satu [Department of Biology, University of Oulu, P.O. Box 3000, FIN-90 014 Finland (Finland)

    2009-08-15

    We analyzed bulk UV absorbance of methanolic extracts and levels of five UV-absorbing compounds (hydroxycinnamic acid derivatives) in 135 herbarium samples of the liverwort Jungermannia exsertifolia subsp. cordifolia from northern Europe. Samples had been collected in 1850-2006 (96% in June-August). Both UV absorbance and compound levels were correlated positively with collection year. p-Coumaroylmalic acid (C1) was the only compound showing a significant (and negative) correlation with stratospheric ozone and UV irradiance in the period that real data of these variables existed. Stratospheric ozone reconstruction (1850-2006) based on C1 showed higher values in June than in July and August, which coincides with the normal monthly variation of ozone. Combining all the data, there was no long-term temporal trend from 1850 to 2006. Reconstructed UV showed higher values in June-July than in August, but again no temporal trend was detected in 1918-2006 using the joint data. This agrees with previous UV reconstructions. - On the basis of the levels of p-coumaroylmalic acid in liverwort samples, reconstructions of both ozone and UV radiation showed no significant temporal trend in, respectively, 1850-2006 and 1918-2006.

  11. Retrospective bioindication of stratospheric ozone and ultraviolet radiation using hydroxycinnamic acid derivatives of herbarium samples of an aquatic liverwort

    International Nuclear Information System (INIS)

    Otero, Saul; Nunez-Olivera, Encarnacion; Martinez-Abaigar, Javier; Tomas, Rafael; Huttunen, Satu

    2009-01-01

    We analyzed bulk UV absorbance of methanolic extracts and levels of five UV-absorbing compounds (hydroxycinnamic acid derivatives) in 135 herbarium samples of the liverwort Jungermannia exsertifolia subsp. cordifolia from northern Europe. Samples had been collected in 1850-2006 (96% in June-August). Both UV absorbance and compound levels were correlated positively with collection year. p-Coumaroylmalic acid (C1) was the only compound showing a significant (and negative) correlation with stratospheric ozone and UV irradiance in the period that real data of these variables existed. Stratospheric ozone reconstruction (1850-2006) based on C1 showed higher values in June than in July and August, which coincides with the normal monthly variation of ozone. Combining all the data, there was no long-term temporal trend from 1850 to 2006. Reconstructed UV showed higher values in June-July than in August, but again no temporal trend was detected in 1918-2006 using the joint data. This agrees with previous UV reconstructions. - On the basis of the levels of p-coumaroylmalic acid in liverwort samples, reconstructions of both ozone and UV radiation showed no significant temporal trend in, respectively, 1850-2006 and 1918-2006.

  12. Acid-base behavior in hydrothermal processing of wastes. 1997 annual progress report

    International Nuclear Information System (INIS)

    1997-01-01

    'A major obstacle to the development of hydrothermal technology for treating DOE wastes has been a lack of scientific knowledge of solution chemistry, thermodynamics and transport phenomena. The progress over the last year is highlighted in the following four abstracts from manuscripts which have been submitted to journals. The authors also have made considerable progress on a spectroscopic study of the acid-base equilibria of Cr(VI). They have utilized novel spectroscopic indicators to study acid-base equilibria up to 380 C. Until now, very few systems have been studied at such high temperatures, although this information is vital for hydrothermal processing of wastes. The pH values of aqueous solutions of boric acid and KOH were measured with the optical indicator 2-naphthol at temperatures from 300 to 380 C. The equilibrium constant Kb-l for the reaction B(OH)3 + OH - = B(OH) -4 was determined from the pH measurements and correlated with a modified Born model. The titration curve for the addition of HCl to sodium borate exhibits strong acid-strong base behavior even at 350 C and 24.1 MPa. At these conditions, aqueous solutions of sodium borate buffer the pH at 9.6 t 0.25. submitted to Ind. Eng. Chem. Res. Acetic Acid and HCl Acid-base titrations for the KOH-acetic acid or NH 3 -acetic acid systems were monitored with the optical indicator 2-naphthoic acid at 350 C and 34 MPa, and those for the HCl;Cl- system with acridine at 380 C and up to 34 MPa (5,000 psia ). KOH remains a much stronger base than NH,OH at high temperature. From 298 K to the critical temperature of water, the dissociation constant for HCl decreases by 13 orders of magnitude, and thus, the basicity of Cl - becomes significant. Consequently, the addition of NaCl to HCl raises the pH. The pH titration curves may be predicted with reasonable accuracy from the relevant equilibrium constants and Pitzer''s formulation of the Debye- Htickel equation for the activity coefficients.'

  13. An overview the boron dilution issue in PWRs

    International Nuclear Information System (INIS)

    Hyvaerinen, J.

    1994-01-01

    The presentation is an overview of boron (boric acid) dilution in pressurized water reactors (PWRs). Boric acid has been widely used in PWRs as a dissolved poison, as one of the main reactivity controlling means, for a long time, from nearly but not quite from the beginning of the design, construction and operation of PWRs in the present-day sense. The specific safety issue, namely the risk of uncontrolled reactivity insertion due to inadvertent boron dilution, is discussed first, followed by a brief look on the history of boron usage in PWRs. A discussion of boron dilution phenomenology is presented next in general terms. Some particular concerns that boron dilution phenomena arouse in the minds of a regulator will also be presented before concluding with a brief look on the future of dissolved poisons. (11 refs.)

  14. Solubilities of iron and nickel oxides under high temperature and high pressure conditions

    International Nuclear Information System (INIS)

    Choi, Ke-Chon; Jung, Yong-Ju; Yeon, Jei-Won; Jee, Kwang-Yong

    2007-01-01

    The purposes of primary coolant chemistry are to assure fuel and material integrity and to minimize out of core radiation fields. During the PWR operation, crud deposits are expected on the cladding, leading to cladding failure and raising the radioactivity. Such deposits come from the corrosion products of system surface. To achieve optimal conditions for primary coolant, basic researches on mass transfer, deposition and solubility of corrosion products are needed. The initial stage of crud formation could be the studies on the solubility of a structural material. It has been known that the solubility of metal oxides in boric acid under high temperature and high pressure condition depends on the pH and dissolved hydrogen. Thus, the effect of various pH on the solubility of metal oxide in boric acid solution was investigated in this work

  15. Study of colloidal particles behaviour in the PWR primary circuit conditions; Etude du comportement des particules colloidales dans les conditions physicochimiques du circuit primaire des reacteurs a eau sous pression

    Energy Technology Data Exchange (ETDEWEB)

    Barale, M

    2006-12-15

    EDF wants to understand, model and limit primary circuit contamination of Pressurized Water Reactors by colloidal particles resulting from corrosion. The electrostatic behaviour of representative oxide particles (cobalt ferrite, nickel ferrite and magnetite) has been studied in primary circuit conditions with the influence of boric acid and lithium hydroxide. The isoelectric point (IEP) and the point of zero charge (PZC) of particles, measured between 5 C and 320 C, exhibit a minimum towards 200 C. The thermodynamic constants of the protonation equilibrium of surface sites were calculated. When boric acid is added, zeta potential and IEP decrease because of borate ions sorption. On the contrary, there is not effect of lithium ions. The modelling of these results under conditions representative of primary circuit shows that these oxides exhibit a negative surface charge, explaining their sorption and adhesion behaviour. (author)

  16. Study of colloidal particles behaviour in the PWR primary circuit conditions

    International Nuclear Information System (INIS)

    Barale, M.

    2006-12-01

    EDF wants to understand, model and limit primary circuit contamination of Pressurized Water Reactors by colloidal particles resulting from corrosion. The electrostatic behaviour of representative oxide particles (cobalt ferrite, nickel ferrite and magnetite) has been studied in primary circuit conditions with the influence of boric acid and lithium hydroxide. The isoelectric point (IEP) and the point of zero charge (PZC) of particles, measured between 5 C and 320 C, exhibit a minimum towards 200 C. The thermodynamic constants of the protonation equilibrium of surface sites were calculated. When boric acid is added, zeta potential and IEP decrease because of borate ions sorption. On the contrary, there is not effect of lithium ions. The modelling of these results under conditions representative of primary circuit shows that these oxides exhibit a negative surface charge, explaining their sorption and adhesion behaviour. (author)

  17. X-ray fluorescence analysis of neodymium oxide/oxalate for rare earth impurities

    International Nuclear Information System (INIS)

    Chandola, L.C.; Mohile, A.N.

    1977-01-01

    An X-ray fluorescence method for the determination of cesium, praseodymium, samarium, europium and gadolinium in pure neodymium oxide and oxalate is described. The oxide sample is converted to oxalate and mixed with a binder (boric acid) to obtain a pressed circular pellet. The amount of sample needed for analysis is reduced by making use of the double layer pellet technique. A tungsten target X-ray tube is employed to irradiate the sample and a Philips PW 1220 semiautomatic X-ray spectrometer with a LiF (200) crystal is used to analyse the fluorescent X-rays. The minimum determination limit is 0.01 percent for all rare earths determined except for europium for which the limit is 0.005 percent. Three sigma detection limits have been calculated. (author)

  18. Comparison of acid leachate and fusion methods to determine plutonium and americium in environmental samples

    International Nuclear Information System (INIS)

    Smith, L.L.; Markun, F.; TenKate, T.

    1992-06-01

    The Analytical Chemistry Laboratory at Argonne National Laboratory performs radiochemical analyses for a wide variety of sites within the Department of Energy complex. Since the chemical history of the samples may vary drastically from site to site, the effectiveness of any analytical technique may also vary. This study compares a potassium fluoride-pyrosulfate fusion technique with an acid leachate method. Both normal and high-fired soils and vegetation samples were analyzed for both americium and plutonium. Results show both methods work well, except for plutonium in high-fired soils. Here the fusion method provides higher accuracy

  19. Development of a New Microextraction Fiber Combined to On-Line Sample Stacking Capillary Electrophoresis UV Detection for Acidic Drugs Determination in Real Water Samples

    Science.gov (United States)

    Araujo, Lilia; Prieto, Avismelsi; Navalón, Alberto; Vílchez, José Luis; Valera, Paola; Zambrano, Ana; Dugas, Vincent

    2017-01-01

    A new analytical method coupling a (off-line) solid-phase microextraction with an on-line capillary electrophoresis (CE) sample enrichment technique was developed for the analysis of ketoprofen, naproxen and clofibric acid from water samples, which are known as contaminants of emerging concern in aquatic environments. New solid-phase microextraction fibers based on physical coupling of chromatographic supports onto epoxy glue coated needle were studied for the off-line preconcentration of these micropollutants. Identification and quantification of such acidic drugs were done by capillary zone electrophoresis (CZE) using ultraviolet diode array detection (DAD). Further enhancement of concentration sensitivity detection was achieved by on-line CE “acetonitrile stacking” preconcentration technique. Among the eight chromatographic supports investigated, Porapak Q sorbent showed higher extraction and preconcentration capacities. The screening of parameters that influence the microextraction process was carried out using a two-level fractional factorial. Optimization of the most relevant parameters was then done through a surface response three-factor Box-Behnken design. The limits of detection and limits of quantification for the three drugs ranged between 0.96 and 1.27 µg∙L−1 and 2.91 and 3.86 µg∙L−1, respectively. Recovery yields of approximately 95 to 104% were measured. The developed method is simple, precise, accurate, and allows quantification of residues of these micropollutants in Genil River water samples using inexpensive fibers. PMID:28686186

  20. Development of a New Microextraction Fiber Combined to On-Line Sample Stacking Capillary Electrophoresis UV Detection for Acidic Drugs Determination in Real Water Samples

    Directory of Open Access Journals (Sweden)

    Maria Espina-Benitez

    2017-07-01

    Full Text Available A new analytical method coupling a (off-line solid-phase microextraction with an on-line capillary electrophoresis (CE sample enrichment technique was developed for the analysis of ketoprofen, naproxen and clofibric acid from water samples, which are known as contaminants of emerging concern in aquatic environments. New solid-phase microextraction fibers based on physical coupling of chromatographic supports onto epoxy glue coated needle were studied for the off-line preconcentration of these micropollutants. Identification and quantification of such acidic drugs were done by capillary zone electrophoresis (CZE using ultraviolet diode array detection (DAD. Further enhancement of concentration sensitivity detection was achieved by on-line CE “acetonitrile stacking” preconcentration technique. Among the eight chromatographic supports investigated, Porapak Q sorbent showed higher extraction and preconcentration capacities. The screening of parameters that influence the microextraction process was carried out using a two-level fractional factorial. Optimization of the most relevant parameters was then done through a surface response three-factor Box-Behnken design. The limits of detection and limits of quantification for the three drugs ranged between 0.96 and 1.27 µg∙L−1 and 2.91 and 3.86 µg∙L−1, respectively. Recovery yields of approximately 95 to 104% were measured. The developed method is simple, precise, accurate, and allows quantification of residues of these micropollutants in Genil River water samples using inexpensive fibers.

  1. Development of a New Microextraction Fiber Combined to On-Line Sample Stacking Capillary Electrophoresis UV Detection for Acidic Drugs Determination in Real Water Samples.

    Science.gov (United States)

    Espina-Benitez, Maria; Araujo, Lilia; Prieto, Avismelsi; Navalón, Alberto; Vílchez, José Luis; Valera, Paola; Zambrano, Ana; Dugas, Vincent

    2017-07-07

    A new analytical method coupling a (off-line) solid-phase microextraction with an on-line capillary electrophoresis (CE) sample enrichment technique was developed for the analysis of ketoprofen, naproxen and clofibric acid from water samples, which are known as contaminants of emerging concern in aquatic environments. New solid-phase microextraction fibers based on physical coupling of chromatographic supports onto epoxy glue coated needle were studied for the off-line preconcentration of these micropollutants. Identification and quantification of such acidic drugs were done by capillary zone electrophoresis (CZE) using ultraviolet diode array detection (DAD). Further enhancement of concentration sensitivity detection was achieved by on-line CE "acetonitrile stacking" preconcentration technique. Among the eight chromatographic supports investigated, Porapak Q sorbent showed higher extraction and preconcentration capacities. The screening of parameters that influence the microextraction process was carried out using a two-level fractional factorial. Optimization of the most relevant parameters was then done through a surface response three-factor Box-Behnken design. The limits of detection and limits of quantification for the three drugs ranged between 0.96 and 1.27 µg∙L -1 and 2.91 and 3.86 µg∙L -1 , respectively. Recovery yields of approximately 95 to 104% were measured. The developed method is simple, precise, accurate, and allows quantification of residues of these micropollutants in Genil River water samples using inexpensive fibers.

  2. Neutron shielding material and a process for producing the same

    International Nuclear Information System (INIS)

    Tadokoro, S.; Segawa, H.

    1982-01-01

    A neutron shielding material comprises a polymerization product of a monomer mixture of an alkyl methacrylate or styrene and a boric acid containing a polyol constituent. Such a material may be formed into transparent sheets with high mechanical strength

  3. Concentrations of higher dicarboxylic acids C5–C13 in fresh snow samples collected at the High Alpine Research Station Jungfraujoch during CLACE 5 and 6

    Directory of Open Access Journals (Sweden)

    K. Sieg

    2009-03-01

    Full Text Available Samples of freshly fallen snow were collected at the high alpine research station Jungfraujoch (Switzerland in February and March 2006 and 2007, during the Cloud and Aerosol Characterization Experiments (CLACE 5 and 6. In this study a new technique has been developed and demonstrated for the measurement of organic acids in fresh snow. The melted snow samples were subjected to solid phase extraction and resulting solutions analysed for organic acids by HPLC-MS-TOF using negative electrospray ionization. A series of linear dicarboxylic acids from C5 to C13 and phthalic acid, were identified and quantified. In several samples the biogenic acid pinonic acid was also observed. In fresh snow the median concentration of the most abundant acid, adipic acid, was 0.69 μg L−1 in 2006 and 0.70 μg L−1 in 2007. Glutaric acid was the second most abundant dicarboxylic acid found with median values of 0.46 μg L−1 in 2006 and 0.61 μg L−1 in 2007, while the aromatic acid phthalic acid showed a median concentration of 0.34 μg L−1 in 2006 and 0.45 μg L−1 in 2007. The concentrations in the samples from various snowfall events varied significantly, and were found to be dependent on the back trajectory of the air mass arriving at Jungfraujoch. Air masses of marine origin showed the lowest concentrations of acids whereas the highest concentrations were measured when the air mass was strongly influenced by boundary layer air.

  4. Porous media investigation before and after hydrochloric acid injection on a pre-salt carbonate coquinas sample.

    Science.gov (United States)

    Machado, A C; Teles, A P; Pepin, A; Bize-Forest, N; Lima, I; Lopes, R T

    2016-04-01

    Porous space characterization of carbonate rocks is an important aid in petroleum exploration from carbonate reservoir. In this study, X-ray microtomography technique was applied to evaluate total porosity of a coquina sample extracted from pre-salt reservoir, in Brazil, before and after acid injection. Two image processing program were used in order to assess performance. The results showed that microtomography has potential to compute porosity of coquina samples and provides information about rock porous network. Copyright © 2016 Elsevier Ltd. All rights reserved.

  5. 40 CFR 180.920 - Inert ingredients used pre-harvest; exemptions from the requirement of a tolerance.

    Science.gov (United States)

    2010-07-01

    ... than 0.2 pt of pesticide formulation Light stabilizer Hydroxypropyl guar gum Thickener Isobornyl... per acre Preservative/stabilizer Boric acid Sequestrant Buffalo gourd root powder (Cucurbita foetidissima root powder); or, Zucchini juice (Cucurbita pepo juice) or Hawkesbury melon Citrullus lanatus. No...

  6. Quantification of fatty acids as methyl esters and phospholipids in cheese samples after separation of triacylglycerides and phospholipids

    International Nuclear Information System (INIS)

    Hauff, Simone; Vetter, Walter

    2009-01-01

    Determination of the individual fatty acid composition of neutral- and phospholipids as well as the phospholipid content of dairy food and other foodstuffs are important tasks in life sciences. For these purposes, a method was developed for the separation of lipids (standards of triolein and diacylphosphatidylcholines as well as three cheese samples) by solid-phase extraction using a self-packed column filled with partly deactivated silica. Non-halogenated solvents were used for the elution of the lipid classes. Cyclohexane/ethyl acetate (1:1, v/v) served for the elution of neutral lipids, while polar lipids were eluted with three solvents (ethyl acetate/methanol, methanol, and methanol/water) into one fraction. The separated lipid fractions were transesterified and the individual fatty acids were quantified by using gas chromatography coupled to electron ionization mass spectrometry (GC/EI-MS) in the selected ion monitoring (SIM) mode. The recovery rate for standard phosphatidylcholines was ∼90% and cross-contamination from neutral lipids was negligible. The method was applied to cheese samples. Quantitative amounts of individual fatty acids in the phospholipid fraction were eq ) were found to be representative for the average contribution of fatty acids to all classes of phospholipids in dairy products. Using this approach, the phospholipid content of lipids from mozzarella, camembert, and goat cream cheese was 0.60%, 1.42% and 0.79%, respectively

  7. Crude protein, fibre and phytic acid in vitro digestibility of selected legume and buckwheat samples

    Directory of Open Access Journals (Sweden)

    Petra Vojtíšková

    2013-01-01

    Full Text Available The aim of this study was to determine crude protein, fibre and phytic acid in vitro digestibility of selected legumes and buckwheat products. All analyses except the phytic acid contents were performed in the line with the Commission Regulation (EC No. 152/2009. A modified version of Holt’s Method was used for phytic acid (phytate determination. None of all samples contained more than 11% of moisture. Soybeans are rich in crude protein; they contain nearly 40% of this compound. The content of crude protein in buckwheat flours was about 14%. The highest amount of phytate was found in common beans and soybeans-about 2 g/100 g of dry matter. On the other hand, the lowest phytate content was observed in buckwheat pasta (F. esculentum groats was 1.9 g per 100 g of dry matter. In vitro digestibility was determined using an incubator Daisy and pepsin enzymes and the combination of pepsin and pancreatin. The highest coefficient of crude protein digestibility was discovered to be in peels and wholemeal flour. The greatest fibre digestibility coefficients were obtained for peels, which contain about 65% of fibre in their dry matter. When pepsin was used, a higher phytic acid digestibility coefficient for G. max, Ph. vulgaris, peels, flour, groats and broken groats was observed; while when the combination of pepsin and pancreatin was used, higher phytic acid digestibility coefficients for peas, lentil and wholemeal flour were observed.

  8. Dependence of matrix effect on ionization polarity during LC-ESI-MS analysis of derivatized amino acids in some natural samples.

    Science.gov (United States)

    Oldekop, Maarja-Liisa; Rebane, Riin; Herodes, Koit

    2017-10-01

    Matrix effect, the influence of co-eluting components on the ionization efficiency of the analyte, affects the trueness and precision of the LC-ESI-MS analysis. Derivatization can reduce or eliminate matrix effect, for example, diethyl ethoxymethylenemalonate (DEEMM) derivatives have shown less matrix effect compared to other derivatives. Moreover, the use of negative ion mode can further reduce matrix effect. In order to investigate the combination of derivatization and different ionization modes, an LC-ESI-MS/MS method using alternating positive/negative ion mode was developed and validated. The analyses in positive and negative ion modes had comparable limit of quantitation values. The influence of ESI polarity on matrix effect was investigated during the analysis of 22 DEEMM-derivatized amino acids in herbal extracts and honeys. Sample dilution approach was used for the evaluation of the presence of matrix effect. Altogether, 4 honeys and 11 herbal extracts were analyzed, and the concentrations of 22 amino acids in the samples are presented. In the positive ion mode, matrix effect was observed for several amino acid derivatives and the matrix effect was stronger in honey samples compared to the herbal extracts. The negative ion mode was free from matrix effect, with only few exceptions in honeys (average relative standard deviation over all analytes and matrices was 8%; SD = 7%). The matrix effect was eliminated in the positive ion mode by sample dilution and agreement between concentrations from the two ion modes was achieved for most amino acids. In conclusion, it was shown that the combination of derivatization and negative ion mode can be a powerful tool for minimizing matrix effect in more complicated applications.

  9. Sample preparation techniques for the determination of natural 15N/14N variations in amino acids by gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS).

    Science.gov (United States)

    Hofmann, D; Gehre, M; Jung, K

    2003-09-01

    In order to identify natural nitrogen isotope variations of biologically important amino acids four derivatization reactions (t-butylmethylsilylation, esterification with subsequent trifluoroacetylation, acetylation and pivaloylation) were tested with standard mixtures of 17 proteinogenic amino acids and plant (moss) samples using GC-C-IRMS. The possible fractionation of the nitrogen isotopes, caused for instance by the formation of multiple reaction products, was investigated. For biological samples, the esterification of the amino acids with subsequent trifluoroacetylation is recommended for nitrogen isotope ratio analysis. A sample preparation technique is described for the isotope ratio mass spectrometric analysis of amino acids from the non-protein (NPN) fraction of terrestrial moss. 14N/15N ratios from moss (Scleropodium spec.) samples from different anthropogenically polluted areas were studied with respect to ecotoxicologal bioindication.

  10. fluconazole and boric acid for treatment of vaginal candidiasis

    African Journals Online (AJOL)

    2013-04-01

    Apr 1, 2013 ... M. K. Khameneie, Assistant Professor, Department of Obstetrics and Gynecology, Imam Reza hospital, Tehran - Iran,. N. Arianpour ..... candidiasis. Am Fam Physician. 2000;1, 61:3306-12. 12. Donders GG, Bellen G, Mendling W. Management of recurrent vulvo-vaginal candidosis as a chronic illness.

  11. Tanzania Journal of Science - Vol 38, No 2 (2012)

    African Journals Online (AJOL)

    Electrical Properties of DC Reactive Magnetron Sputtered ZnO:Al Films from Optical ... of ZnO:Al/ZnO Double Layers and the Cu(In,Ga)Se2 Solar Cell Efficiencies · EMAIL ... Management of Azole-Refractory Candida Species Using Boric Acid ...

  12. Neutron shielding material and process for its manufacture

    International Nuclear Information System (INIS)

    Tadokoro, S.I; Segawa, H.

    1980-01-01

    The artificial resin sheets are optically transparent and mechanically strong. They are the polymerisation product of methyl methacrylate and a boric acid ester, for example. The boron content of the material is between 1% and 6% by weight (many examples). (RW) [de

  13. Utilization of borosilicate glass for transuranic waste immobilization

    International Nuclear Information System (INIS)

    Ledford, J.A.; Williams, P.M.

    1979-01-01

    Incinerated transuranic waste and other low-level residues have been successfully vitrified by mixing with boric acid and sodium carbonate and heating to 1050 0 C in a bench-scale continuous melter. The resulting borosilicate glass demonstrates excellent mechanical durability and chemical stability

  14. Focused-microwave-assisted sample preparation (M8)

    International Nuclear Information System (INIS)

    Nobrega, J.A.; Santos, D.M.; Trevizan, L.C.; Costa, L.M.; Nogueira, A.R.A.

    2002-01-01

    Full text: Focused-microwave-assisted sample preparation is a suitable strategy when dealing with high masses of organic samples. However, the final acid concentration of the digestate can difficult routine analytical measurements using spectroscopic techniques. Acids could be evaporated, but this step could be slow even when using microwave-assisted heating and requires a scrubber system for acid vapor collection and neutralization. We are investigating two procedures to decrease the acid concentration of digestates. The first one is based on acid vapor phase digestion of samples contained in PTFE devices' inserted into the microwave flask. The acid solution is heated by absorption of microwave radiation, then the acid vapor partially condenses in the upper part of the reaction flask and it is partially collected in each sample container. Calcium, Fe, Mg, Mn, and Zn were quantitatively recovered in samples of animal and vegetable tissues. Better recoveries were attained when adding a small volume of sodium hypochlorite to the sample. This effect is probably related to the generation of chlorine in the sample container after collecting condensed acid. The second procedure developed is based on the gradual addition of liquid samples to a previously heated acid digestion mixture. This procedure was successfully applied for digestion of milk, fruit juices, and red wine. The main advantage is the possibility of digesting up to four-fold more sample using up to ten-fold lower amounts of concentrated acids. Results obtained using both digestion procedures and measurements by ICP-OES with axial view will be presented. (author)

  15. A novel digestion method based on a choline chloride–oxalic acid deep eutectic solvent for determining Cu, Fe, and Zn in fish samples

    Energy Technology Data Exchange (ETDEWEB)

    Habibi, Emadaldin [Department of Marine Chemistry, Faculty of Marine Science, Khorramshahr University of Marine Science and Technology, P.O. BOX 669, Khorramshahr (Iran, Islamic Republic of); Ghanemi, Kamal, E-mail: Kamal.ghanemi@kmsu.ac.ir [Department of Marine Chemistry, Faculty of Marine Science, Khorramshahr University of Marine Science and Technology, P.O. BOX 669, Khorramshahr (Iran, Islamic Republic of); Marine Science Research Institute, Khorramshahr University of Marine Science and Technology, Khorramshahr (Iran, Islamic Republic of); Fallah-Mehrjardi, Mehdi [Department of Marine Chemistry, Faculty of Marine Science, Khorramshahr University of Marine Science and Technology, P.O. BOX 669, Khorramshahr (Iran, Islamic Republic of); Marine Science Research Institute, Khorramshahr University of Marine Science and Technology, Khorramshahr (Iran, Islamic Republic of); Dadolahi-Sohrab, Ali [Department of Marine Environment, Faculty of marine natural resources, Khorramshahr University of Marine Science and Technology, Khorramshahr (Iran, Islamic Republic of)

    2013-01-31

    Highlights: ► A novel digestion method: lack of concentrated acids or oxidizing reagents. ► First report of using choline chloride–oxalic acid (ChCl–Ox) for digestion. ► Complete dissolution of biological samples in ChCl–Ox for solubilization metals. ► Extraction recoveries greater than 95%: validated by the fish protein CRM. ► Successfully applied in different fish tissues (Muscle, Liver, and Gills). -- Abstract: A novel and efficient digestion method based on choline chloride–oxalic acid (ChCl–Ox) deep eutectic solvent (DES) was developed for flame atomic absorption spectrometry (FAAS) determination of Cu, Zn, and Fe in biological fish samples. Key parameters that influence analyte recovery were investigated and optimized, using the fish protein certified reference material (CRM, DORM-3) throughout the procedure. In this method, 100 mg of the sample was dissolved in ChCl–Ox (1:2, molar ratio) at 100 °C for 45 min. Then, 5.0 mL HNO{sub 3} (1.0 M) was added. After centrifugation, the supernatant solution was filtered, diluted to a known volume, and analyzed by FAAS. Under optimized conditions, an excellent agreement between the obtained results and the certified values was observed, using Student's t-test (P = 0.05); the extraction recovery of the all elements was greater than 95.3%. The proposed method was successfully applied to the determination of analytes in different tissues (muscle, liver, and gills) having a broad concentration range in a marine fish sample. The reproducibility of the method was validated by analyzing all samples by our method in a different laboratory, using inductively coupled plasma optical emission spectrometry (ICP-OES). For comparison, a conventional acid digestion (CAD) method was also used for the determination of analytes in all studied samples. The simplicity of the proposed experimental procedure, high extraction efficiency, short analysis time, lack of concentrated acids and oxidizing agents, and the

  16. A novel digestion method based on a choline chloride–oxalic acid deep eutectic solvent for determining Cu, Fe, and Zn in fish samples

    International Nuclear Information System (INIS)

    Habibi, Emadaldin; Ghanemi, Kamal; Fallah-Mehrjardi, Mehdi; Dadolahi-Sohrab, Ali

    2013-01-01

    Highlights: ► A novel digestion method: lack of concentrated acids or oxidizing reagents. ► First report of using choline chloride–oxalic acid (ChCl–Ox) for digestion. ► Complete dissolution of biological samples in ChCl–Ox for solubilization metals. ► Extraction recoveries greater than 95%: validated by the fish protein CRM. ► Successfully applied in different fish tissues (Muscle, Liver, and Gills). -- Abstract: A novel and efficient digestion method based on choline chloride–oxalic acid (ChCl–Ox) deep eutectic solvent (DES) was developed for flame atomic absorption spectrometry (FAAS) determination of Cu, Zn, and Fe in biological fish samples. Key parameters that influence analyte recovery were investigated and optimized, using the fish protein certified reference material (CRM, DORM-3) throughout the procedure. In this method, 100 mg of the sample was dissolved in ChCl–Ox (1:2, molar ratio) at 100 °C for 45 min. Then, 5.0 mL HNO 3 (1.0 M) was added. After centrifugation, the supernatant solution was filtered, diluted to a known volume, and analyzed by FAAS. Under optimized conditions, an excellent agreement between the obtained results and the certified values was observed, using Student's t-test (P = 0.05); the extraction recovery of the all elements was greater than 95.3%. The proposed method was successfully applied to the determination of analytes in different tissues (muscle, liver, and gills) having a broad concentration range in a marine fish sample. The reproducibility of the method was validated by analyzing all samples by our method in a different laboratory, using inductively coupled plasma optical emission spectrometry (ICP-OES). For comparison, a conventional acid digestion (CAD) method was also used for the determination of analytes in all studied samples. The simplicity of the proposed experimental procedure, high extraction efficiency, short analysis time, lack of concentrated acids and oxidizing agents, and the use of

  17. Boron isotope separation by ion exchange chromatography using weakly basic anion exchange resin

    International Nuclear Information System (INIS)

    Sakuma, Yoichi; Aida, Masao; Okamoto, Makoto; Kakihana, Hidetake

    1980-01-01

    Isotopic plateau displacement chromatography, a useful method for isotope separation is presented. The boric acid band formed in a column of weakly basic anion exchange resin Diaion WA21 can be eluted with pure water. In order to obtain good accumulation of the isotope effect, a series of experiments with different migration length were carried out. The boron-10 enriched part of the boric acid absorbed band was always preceded by the isotopic plateau part, in which the atomic fraction of boron-10 was maintained at its original value. The atomic fraction of boron-10 at the end of the chromatogram increased with migration length, and in the case of 256-m migration, boron-10 was enriched from its original atomic fraction of 19.84 to 91.00%, the separation factor S being constant irrespective of migration length: S = 1.0100 +- 0.0005. (author)

  18. Post-LOCA core flushing system

    International Nuclear Information System (INIS)

    Boyajian, J.D.; Weinberger, P.A.

    1980-01-01

    A system is disclosed for flushing the core of a nuclear reactor after a loss-of-coolant accident. A pump causes flow of liquid-phase fluid from the containment-vessel sump. This flow is used to provide the motivating force for an eductor that causes suction at the hot log of the reactor. The eductor suction can draw gas-phase coolant out of the hot leg. As a result, it can reduce pressure which may be preventing the flow of liquid-phase coolant out of the hot leg. By causing liquid-phase flow through the reactor, the system ensures that particles and boric acid are flushed out of the core. The system thereby eliminates the build-up of particles and the concentrations of boric acid in the core that could result if the coolant were to leave the pressure vessel exclusively in the gas phase. 9 claims

  19. Crack propagation rate modelling for 316SS exposed to PWR-relevant conditions

    International Nuclear Information System (INIS)

    Vankeerberghen, M.; Weyns, G.; Gavrilov, S.; Martens, B.; Deconinck, J.

    2009-01-01

    The crack propagation rate of Type 316 stainless steel in boric acid-lithium hydroxide solutions under PWR-relevant conditions was modelled. A film rupture/dissolution/repassivation mechanism is assumed and extended to cold worked materials by including a stress-dependent bare metal dissolution current density. The chemical and electrochemical conditions within the crack are calculated by finite element calculations, an analytical expression is used for the crack-tip strain rate and the crack-tip stress is assumed equal to 2.5 times the yield stress (plane-strain). First the model was calibrated against a literature published data set. Afterwards, the influence of various variables - dissolved hydrogen, boric acid and lithium hydroxide content, stress intensity, crack length, temperature, flow rate - was studied. Finally, other published crack growth rate tests were modelled and the calculated crack growth rates were found to be in reasonable agreement with the reported ones

  20. Probe depth matters in dermal microdialysis sampling of benzoic acid after topical application

    DEFF Research Database (Denmark)

    Holmgaard, R; Benfeldt, E; Bangsgaard, N

    2012-01-01

    -2 mm) and deep (>2 mm) positioning of the linear MD probe in the dermis of human abdominal skin, followed by topical application of 4 mg/ml of benzoic acid (BA) in skin chambers overlying the probes. Dialysate was sampled every hour for 12 h and analysed for BA content by high-performance liquid...... chromatography. Probe depth was measured by 20-MHz ultrasound scanning. The area under the time-versus-concentration curve (AUC) describes the drug exposure in the tissue during the experiment and is a relevant parameter to compare for the 3 dermal probe depths investigated. The AUC(0-12) were: superficial...... significantly different from each other (p value paper demonstrates that there is an inverse relationship between the depth of the probe in the dermis and the amount of drug sampled following topical penetration ex vivo. The result is of relevance to the in vivo situation, and it can...

  1. X-ray fluorescence analysis of praseodymium oxide/oxalate for rare earth impurities

    International Nuclear Information System (INIS)

    Chandola, L.C.; Mohile, A.N.

    1976-01-01

    A method for the determination of lanthanum, cerium, neodymium and samarium oxides in praseodymium oxide is described. The sample in the oxalate form is mixed with boric acid binder in the weight ratio of 1:1 and pressed into a pellet. The pellet is irradiated by X-rays from a tungsten tube and fluorescent X-rays are dispersed by a LiF (200) crystal in a Philips semiautomatic X-ray fluorescence spectrometer. The intensity of the characteristic X-rays of the impurity elements is measured by a flow proportional counter at selected 20 angles. The minium determination limit is 0.01% for all impurities. (author)

  2. Limited sampling strategies drawn within 3 hours postdose poorly predict mycophenolic acid area-under-the-curve after enteric-coated mycophenolate sodium.

    NARCIS (Netherlands)

    Winter, B.C. de; Gelder, T. van; Mathôt, R.A.A.; Glander, P.; Tedesco-Silva, H.; Hilbrands, L.B.; Budde, K.; Hest, R.M. van

    2009-01-01

    Previous studies predicted that limited sampling strategies (LSS) for estimation of mycophenolic acid (MPA) area-under-the-curve (AUC(0-12)) after ingestion of enteric-coated mycophenolate sodium (EC-MPS) using a clinically feasible sampling scheme may have poor predictive performance. Failure of

  3. Silver nanoparticles plasmon resonance-based method for the determination of uric acid in human plasma and urine samples

    International Nuclear Information System (INIS)

    Amjadi, M.; Rahimpour, E.

    2012-01-01

    We have developed a simple and sensitive colorimetric procedure for the quantification of trace amounts of uric acid. It is based on the finding that uric acid in a medium containing ammonia and sodium hydroxide at 65 0 C can reduce silver ions to form yellow silver nanoparticles (Ag NPs). These are stabilized in solution by using poly(vinyl alcohol) as a capping agent. The yellow color of the solution that results from the localized surface plasmon resonance of Ag NPs can be observed by the bare eye. The absorbance at 415 nm is proportional to the concentration of uric acid which therefore can be determined quantitatively. The calibration curve is linear in the concentration range from 10 to 200 nM, with a limit of detection of 3.3 nM. The method was successfully applied to the determination of uric acid in human plasma and urine samples. (author)

  4. Use of FTA cards for the storage of breast carcinoma nucleic acid on fine-needle aspiration samples.

    Science.gov (United States)

    Peluso, Anna Lucia; Cascone, Anna Maria; Lucchese, Lucrezia; Cozzolino, Immacolata; Ieni, Antonio; Mignogna, Chiara; Pepe, Stefano; Zeppa, Pio

    2015-10-01

    The preservation and storage of nucleic acids is important for DNA molecular techniques. The material obtained by fine-needle aspiration (FNA) is often scanty and can not be wasted. FTA cards are filter papers that immobilize and stabilize nucleic acids and can be stored at room temperature. The current study evaluated whether nucleic acids of breast carcinoma cells, obtained by FNA in a clinical setting, may be collected, stored, and preserved on FTA cards. Thirty breast carcinoma, 5 non-Hodgkin lymphoma (NHL), and 5 benign reactive lymph node (RLN) cell samples obtained by FNA were stored at -80 °C and on FTA cards. DNA extraction and polymerase chain reaction were performed on cells at -80 °C and on 2 punched disks of FTA cards. Fifty nanograms of extracted DNA from both sample types were used to amplify the Janus Kinase 2 (JAK2) gene. The mean value of DNA extracted from breast carcinoma cells was 28.19 ng/µL for that stored at -80 °C and 3.28 ng/µL for that stored on FTA cards. Agarose gel analysis demonstrated expected bands of DNA in 29 cases (97%) with both methods. The mean value of DNA extracted from NHL and RLN samples was 37.54 ng/µL and 4.28 ng/µL, respectively, and agarose gel analysis demonstrated bands of high molecular weight DNA in both methods. Significant differences in DNA yield were found between storage at -80 °C and FTA cards (PFTA cards can be conveniently used for the storage of breast carcinoma cells obtained by FNA, thus providing a reliable alternative to traditional methods. © 2015 American Cancer Society.

  5. Long-Endurance Maritime Surveillance with Ocean Glider Networks

    Science.gov (United States)

    2015-09-01

    response to fluid viscosity , as well as magnesium sulfate and boric acid molecules found in seawater (Francois and Garrison 1982). As a result, its...Hemipelagic Terrigenous Clay ) is derived from the Bottom Sediment Type (BST) database maintained by the U.S. Naval Oceanographic Office Acoustics

  6. Proceedings: 1991 EPRI workshop on secondary-side intergranular corrosion mechanisms

    International Nuclear Information System (INIS)

    Partridge, M.J.; Zemitis, W.S.

    1992-08-01

    A workshop on ''Secondary-Side Intergranular Corrosion Mechanisms'' was organized by EPRI as an effort to give those working in this area an opportunity to share their results, ideas, and plans. Topics covered included: (1) caustic induced intergranular attack/stress corrosion cracking (IGA/IGSCC), (2) plant experience, (3) boric acid as an IGA/IGSCC remedial measure, (4) lead induced IGA/IGSCC, and (5) acid induced IGA/IGSCC

  7. The Consistency of Isotopologues of Ambient Atmospheric Nitric Acid in Passively Collected Samples

    Science.gov (United States)

    Bell, M. D.; Sickman, J. O.; Bytnerowicz, A.; Padgett, P.; Allen, E. B.

    2012-12-01

    Anthropogenic sources of nitrogen oxides have previously been shown to have distinctive isotopic signatures of oxygen and nitrogen. Nylon filters are currently used in passive sampling arrays to measure ambient atmospheric nitric acid concentrations and estimate deposition rates. This experiment measured the ability of nylon filters to consistently collect isotopologues of atmospheric nitric acid in the same ratios as they are present in the atmosphere. Samplers were deployed in continuous stirred tank reactors (CSTR) and at field sites across a nitrogen deposition gradient in Southern California. Filters were exposed over a four week period with individual filters being subjected to 1-4 week exposure times. Extracted nitric acid were measured for δ18O and δ15N ratios and compared for consistency based on length of exposure and amount of HNO3 collected. Filters within the CSTRs collected HNO3 at a consistent rate in both high and low concentration chambers. After two weeks of exposure, the mean δ18O values were within 0.5‰ of the δ18O of the source HNO3 solution. The mean of all weekly exposures were within 0.5‰ of the δ15N of the source solution, but after three weeks, the mean δ15N of adsorbed HNO3 was within 0.2‰. As the length of the exposure increased, the variability of measured delta values decreased for both elements. The field samplers collected HNO3 consistent with previously measured values along a deposition gradient. The mean δ18O at high deposition sites was 52.2‰ compared to 35.7‰ at the low deposition sites. Mean δ15N values were similar at all sites across the deposition gradient. Due to precipitation events occurring during the exposure period, the δ15N and δ18O of nitric acid were highly variable at all field sites. At single sites, changes in δ15N and δ18O were negatively correlated, consistent with two-sourcing mixing dynamics, but the slope of the regressions differed between high and low deposition sites. Anthropogenic

  8. Optimized methods for total nucleic acid extraction and quantification of the bat white-nose syndrome fungus, Pseudogymnoascus destructans, from swab and environmental samples.

    Science.gov (United States)

    Verant, Michelle L; Bohuski, Elizabeth A; Lorch, Jeffery M; Blehert, David S

    2016-03-01

    The continued spread of white-nose syndrome and its impacts on hibernating bat populations across North America has prompted nationwide surveillance efforts and the need for high-throughput, noninvasive diagnostic tools. Quantitative real-time polymerase chain reaction (qPCR) analysis has been increasingly used for detection of the causative fungus, Pseudogymnoascus destructans, in both bat- and environment-associated samples and provides a tool for quantification of fungal DNA useful for research and monitoring purposes. However, precise quantification of nucleic acid from P. destructans is dependent on effective and standardized methods for extracting nucleic acid from various relevant sample types. We describe optimized methodologies for extracting fungal nucleic acids from sediment, guano, and swab-based samples using commercial kits together with a combination of chemical, enzymatic, and mechanical modifications. Additionally, we define modifications to a previously published intergenic spacer-based qPCR test for P. destructans to refine quantification capabilities of this assay. © 2016 The Author(s).

  9. Optimized methods for total nucleic acid extraction and quantification of the bat white-nose syndrome fungus, Pseudogymnoascus destructans, from swab and environmental samples

    Science.gov (United States)

    Verant, Michelle; Bohuski, Elizabeth A.; Lorch, Jeffrey M.; Blehert, David

    2016-01-01

    The continued spread of white-nose syndrome and its impacts on hibernating bat populations across North America has prompted nationwide surveillance efforts and the need for high-throughput, noninvasive diagnostic tools. Quantitative real-time polymerase chain reaction (qPCR) analysis has been increasingly used for detection of the causative fungus, Pseudogymnoascus destructans, in both bat- and environment-associated samples and provides a tool for quantification of fungal DNA useful for research and monitoring purposes. However, precise quantification of nucleic acid fromP. destructans is dependent on effective and standardized methods for extracting nucleic acid from various relevant sample types. We describe optimized methodologies for extracting fungal nucleic acids from sediment, guano, and swab-based samples using commercial kits together with a combination of chemical, enzymatic, and mechanical modifications. Additionally, we define modifications to a previously published intergenic spacer–based qPCR test for P. destructans to refine quantification capabilities of this assay.

  10. Nitrosation and Nitration of Fulvic Acid, Peat and Coal with Nitric Acid.

    Directory of Open Access Journals (Sweden)

    Kevin A Thorn

    Full Text Available Nitrohumic acids, produced from base extraction of coals and peats oxidized with nitric acid, have received considerable attention as soil ammendments in agriculture. The nitration chemistry however is incompletely understood. Moreover, there is a need to understand the reaction of nitric acid with natural organic matter (NOM in general, in the context of a variety of environmental and biogeochemical processes. Suwannee River NOM, Suwannee River fulvic acid, and Pahokee Peat fulvic acid were treated with 15N-labeled nitric acid at concentrations ranging from 15% to 22% and analyzed by liquid and solid state 15N NMR spectroscopy. Bulk Pahokee peat and Illinois #6 coal were also treated with nitric acid, at 29% and 40% respectively, and analyzed by solid state 15N NMR spectroscopy. In addition to nitro groups from nitration of aromatic carbon, the 15N NMR spectra of all five samples exhibited peaks attributable to nitrosation reactions. These include nitrosophenol peaks in the peat fulvic acid and Suwannee River samples, from nitrosation of phenolic rings, and N-nitroso groups in the peat samples, from nitrosation of secondary amides or amines, the latter consistent with the peat samples having the highest naturally abundant nitrogen contents. Peaks attributable to Beckmann and secondary reactions of the initially formed oximes were present in all spectra, including primary amide, secondary amide, lactam, and nitrile nitrogens. The degree of secondary reaction product formation resulting from nitrosation reactions appeared to correlate inversely with the 13C aromaticities of the samples. The nitrosation reactions are most plausibly effected by nitrous acid formed from the reduction of nitric acid by oxidizable substrates in the NOM and coal samples.

  11. A p An atte proces empt t ss of da oward awada s stan awan b ...

    African Journals Online (AJOL)

    SAM

    2014-08-07

    Aug 7, 2014 ... used as “sorrel meat” or Iyu (Schippers, 2000) and Borno where the .... copper sulphate (CuSO4) and selenium oxide (SeO2) in the ratio. 10:5:1 was ... boric acid containing four drops of bromocresol green/methyl red indicator ...

  12. Multielement determination of major-to-ultratrace elements in vegetable samples by ICP-MS and ICP-AES after acid digestion

    Energy Technology Data Exchange (ETDEWEB)

    Hokura, Akiko; Oguri, Sachiko; Matsuura, Hirotaka; Haraguchi, Hiroki [Dept. of Applied Chemistry, Graduate School of Engineering, Nagoya Univ. (Japan)

    2000-06-01

    A multielement determination of major-to-ultratrace elements in vegetable samples was carried out by inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma atomic emission spectrometry (ICP-AES). Spinach samples (0.5 g) were digested with nitric acid and hydrofluoric acid in a Teflon beaker on a hot plate. The decomposed samples were dissolved in a 1 M ( = mol dm{sup -3}) HNO{sub 3} solution containing internal standard elements (Ge, In, and Re, 10 ppb each), and were subjected to multielement analyses by ICP-AES and ICP-MS. As a result, about 40 elements were successfully determined over a wide concentration range from % to ppb level. Spinach samples grown in different production areas were also analyzed in order to understand the influences of the environmental conditions on growth. Among the major and minor elements, the values of the coefficient of variance (CV) for B, Mg, P, and K were < 20%, and those for Ca, Na, Al, and Mn were higher than 50%. On the other hand, the values of CV for trace and ultratrace elements were significantly high. Furthermore, the present analytical method was also applied to the determination of major-to-ultratrace elements in various vegetable samples (23 species in 11 families); the similarities and differences of the elemental distributions in vegetables were found in the experimental results. (author)

  13. Multielement determination of major-to-ultratrace elements in vegetable samples by ICP-MS and ICP-AES after acid digestion

    International Nuclear Information System (INIS)

    Hokura, Akiko; Oguri, Sachiko; Matsuura, Hirotaka; Haraguchi, Hiroki

    2000-01-01

    A multielement determination of major-to-ultratrace elements in vegetable samples was carried out by inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma atomic emission spectrometry (ICP-AES). Spinach samples (0.5 g) were digested with nitric acid and hydrofluoric acid in a Teflon beaker on a hot plate. The decomposed samples were dissolved in a 1 M ( = mol dm -3 ) HNO 3 solution containing internal standard elements (Ge, In, and Re, 10 ppb each), and were subjected to multielement analyses by ICP-AES and ICP-MS. As a result, about 40 elements were successfully determined over a wide concentration range from % to ppb level. Spinach samples grown in different production areas were also analyzed in order to understand the influences of the environmental conditions on growth. Among the major and minor elements, the values of the coefficient of variance (CV) for B, Mg, P, and K were < 20%, and those for Ca, Na, Al, and Mn were higher than 50%. On the other hand, the values of CV for trace and ultratrace elements were significantly high. Furthermore, the present analytical method was also applied to the determination of major-to-ultratrace elements in various vegetable samples (23 species in 11 families); the similarities and differences of the elemental distributions in vegetables were found in the experimental results. (author)

  14. New Acid Combination for a Successful Sandstone Acidizing

    Science.gov (United States)

    Shafiq, M. U.; Mahmud, H. K. B.; Rezaee, R.

    2017-05-01

    With the development of new enhanced oil recovery techniques, sandstone acidizing has been introduced and played a pivotal role in the petroleum industry. Different acid combinations have been applied, which react with the formation, dissolve the soluble particles; thus increase the production of hydrocarbons. To solve the problems which occurred using current preflush sandstone acidizing technology (hydrochloric acid); a new acid combination has been developed. Core flooding experiments on sandstone core samples with dimensions 1.5 in. × 3 in. were conducted at a flow rate of 2 cm3/min. A series of hydrochloric-acetic acid mixtures with different ratios were tested under 150°F temperature. The core flooding experiments performed are aimed to dissolve carbonate, sodium, potassium and calcium particles from the core samples. These experiments are followed by few important tests which include, porosity-permeability, pH value, Inductively Coupled Plasma (ICP) analysis and Nuclear Magnetic Resonance (NMR measurements). All the results are compared with the results of conventional hydrochloric acid technology. NMR and porosity analysis concluded that the new acid combination is more effective in creating fresh pore spaces and thus increasing the reservoir permeability. It can be seen from the pore distribution before and after the acidizing. Prior applying acid; the large size of pores appears most frequently in the pore distribution while with the applied acid, it was found that the small pore size is most the predominant of the pore distribution. These results are validated using ICP analysis which shows the effective removal of calcium and other positive ions from the core sample. This study concludes that the combination of acetic-hydrochloric acid can be a potential candidate for the preflush stage of sandstone acidizing at high temperature reservoirs.

  15. Analyses of CsI aerosol deposition in aerosol behavior tests in WIND project

    International Nuclear Information System (INIS)

    Kudo, Tamotsu; Shibazaki, Hiroaki; Hidaka, Akihide

    1999-01-01

    The aerosol deposition tests have been performed in WIND project at JAERI to characterize the aerosol behavior. The aerosol deposition tests named WAV1-D and WAV2-D were analyzed by aerosol behavior analysis codes, JAERI's ART and SNL's VICTORIA. The comparison calculation was performed for the confirmation of the analytical capabilities of the both codes and improvement of the models in ART. The deposition mass calculated by ART was larger than that by VICTORIA. This discrepancy is caused by differences in model for FP vapor condensation onto the wall surface. In the WAV2-D test, in which boric acid was placed on the floor area of the test section prior to the deposition phase to simulate the PWR primary coolant, there was a discrepancy in deposition mass between analytical results in both codes and experimental results. The discrepancy may be caused by existence of boric acid which is not considered in the codes. (author)

  16. In vitro evaluation of boron tolerance in wheat (Triticum aestivum L. genotypes

    Directory of Open Access Journals (Sweden)

    Kondić-Špika Ankica

    2010-01-01

    Full Text Available Wheat tolerance to high boron concentrations was determined using mature embryo culture. The testing was performed on a modified MS nutrient medium to which boric acid was added in two concentrations: 15 mM and 30 mM. The control medium contained no excess boric acid. The experiment involved 14 Serbian varieties. After one month of cultivation callus fresh weight (CFW was measured and reductions of fresh callus weight (RFCW at boron (B concentration of 15 mM in relation to the control were calculated. The genotypes differed significantly according to their reaction to different B concentrations. Six genotypes had RFCWs below 50.0 %, while eight genotypes had RFCWs above 50.1 %. Cultivars Nevesinjka and Pesma were considered the most tolerant genotypes, while cultivars Balada and Vila were the most sensitive. The results confirmed that differences in genotype reactions to excess B are visible at the cellular level and that they may serve as a selection criterion. .

  17. Calculation of spatial weighting functions for ex-core detectors of VVER-440 reactors by Monte Carlo method

    International Nuclear Information System (INIS)

    Berki, T.

    2003-01-01

    The signal of ex-core detectors depends not only on the total power of a reactor but also on the power distribution. The spatial weighting function establishes correspondence between the power distribution and the detector signal. The weighting function is independent of the power distribution. The weighting function is used for detector-response analyses, for example in the case of rod-drop experiments. (1) The paper describes the calculation and analysis of the weighting function of a VVER-440. The three-dimensional Monte Carlo code MCNP is used for the evaluation. Results from forward and adjoint calculations are compared. The effect of the change in the concentration of boric acid is also investigated. The evaluation of the spatial weighting function is a fixed-source neutron transport problem, which can be solved much faster by adjoint calculation, however forward calculations provide more detailed results. It is showed that the effect of boric acid upon the weighting function is negligible. (author)

  18. GDP-D-mannose epimerase regulates male gametophyte development, plant growth and leaf senescence in Arabidopsis.

    Science.gov (United States)

    Qi, Tiancong; Liu, Zhipeng; Fan, Meng; Chen, Yan; Tian, Haixia; Wu, Dewei; Gao, Hua; Ren, Chunmei; Song, Susheng; Xie, Daoxin

    2017-09-04

    Plant GDP-D-mannose epimerase (GME) converts GDP-D-mannose to GDP-L-galactose, a precursor of both L-ascorbate (vitamin C) and cell wall polysaccharides. However, the genetic functions of GME in Arabidopsis are unclear. In this study, we found that mutations in Arabidopsis GME affect pollen germination, pollen tube elongation, and transmission and development of the male gametophyte through analysis of the heterozygous GME/gme plants and the homozygous gme plants. Arabidopsis gme mutants also exhibit severe growth defects and early leaf senescence. Surprisingly, the defects in male gametophyte in the gme plants are not restored by L-ascorbate, boric acid or GDP-L-galactose, though boric acid rescues the growth defects of the mutants, indicating that GME may regulate male gametophyte development independent of L-ascorbate and GDP-L-galactose. These results reveal key roles for Arabidopsis GME in reproductive development, vegetative growth and leaf senescence, and suggest that GME regulates plant growth and controls male gametophyte development in different manners.

  19. Natural convection type reactor

    International Nuclear Information System (INIS)

    Nakayama, Takafumi; Horiuchi, Tetsuo; Moriya, Kimiaki; Matsumoto, Masayoshi; Akita, Minoru.

    1988-01-01

    Purpose: To improve the reliability by decreasing the number of dynamic equipments and safely shutdown the reactor core upon occurrence of accidents. Constitution: A pressure relief valve and a pressurizing tank or gravitational water falling tank disposed to the main steam pipe of a reactor are installed in combination. Upon loss-of-coolant accident, the pressure relief valve is opened to reduce the pressure in the reactor pressure vessel to the operation pressure for each of the tanks, thereby enabling to inject water in the pressurizing tank at first and, thereafter, water in the gravitational water falling tank successively to the inside of the pressure vessel. By utilizing the natural force in this way, the reliability can be improved as compared with the case of pumped water injection. Further, by injecting an aqueous boric acid to a portion of a plurality of tanks, if the control rod insertion becomes impossible, aqueous boric acid can be injected. (Takahashi, M.)

  20. Corrosion resistance testing of high-boron-content stainless steels

    International Nuclear Information System (INIS)

    Petrman, I.; Safek, V.

    1994-01-01

    Boron steels, i.e. stainless steels with boron contents of 0.2 to 2.25 wt.%, are employed in nuclear engineering for the manufacture of baskets or wells in which radioactive fissile materials are stored, mostly spent nuclear fuel elements. The resistance of such steels to intergranular corrosion and uniform corrosion was examined in the Strauss solution and in boric acid; the dependence of the corrosion rate of the steels on their chemical composition was investigated, and their resistance was compared with that of AISI 304 type steel. Corrosion resistance tests in actual conditions of ''wet'' compact storage (demineralized water or a weak boric acid solution) gave evidence that boron steels undergo nearly no uniform corrosion and, as electrochemical measurements indicated, match standard corrosion-resistant steels. Corrosion resistance was confirmed to decrease slightly with increasing boron content and to increase somewhat with increasing molybdenum content. (Z.S.). 3 tabs., 4 figs., 7 refs

  1. Method of manufacturing neutron protecting materials

    Energy Technology Data Exchange (ETDEWEB)

    Kakibana, Hidetake; Okamoto, Masazane; Fujii, Yasuhiko; Koguchi, Noboru; Takesute, Morihito; Miyamatsu, Tokuhisa

    1985-06-03

    Purpose: To manufacture neutron protecting materials which are highly flexible and can be shaped with ease at a good workability. Method: In this invention, natural lithium, natural boron such as Li-6 or B-10 or enriched isotope thereof with a great neutron absorption cross section is fixed to fibers. As a specific example, lumps of copolymer fibers are fabricated into weave sheets in a carding machine and applied with needle punching to prepare felt-like products. They are conditioned to OH or H type, which are respectively immersed in saturated aqueous boric acid or 1M-aqueous solution of lithium hydroxide and then dewatered and dried. As a result, boric acid type anion exchange fibers and lithium type cation exchange fibers can be obtained from the former and the latter respectively. In this way, blankets or cloths which are light in weight, flexible and have high neutron absorbing performance can be shaped. They are also in good fitting contact to a human body. (Kamimura, M.).

  2. Comparison of hot hydroxylamine hydrochloride and oxalic acid leaching of stream sediment and coated rock samples as anomaly enhancement techniques

    Science.gov (United States)

    Filipek, L.H.; Chao, T.T.; Theobald, P.K.

    1982-01-01

    A hot hydroxylamine hydrochloride (H-Hxl) extraction in 25% acetic acid is compared with the commonly used oxalic acid extraction as a method of anomaly enhancement for Cu and Zn in samples from two very different metal deposits and climatic environments. Results obtained on minus-80-mesh stream sediments from an area near the Magruder massive sulfide deposit in Lincoln County, Georgia, where the climate is humid subtropical, indicate that H-Hxl enhances the anomaly for Cu by a factor of 2 and for Zn by a factor of 1.5, compared to the oxalic method. Analyses of Fe oxide-coated rock samples from outcrops overlying the North Silver Bell porphyry copper deposit near Tucson, Arizona, where the climate is semi-arid to arid, indicate that both techniques effectively outline the zones of hydrothermal alteration. The H-Hxl extraction can also perform well in high-carbonate or high-clay environments, where other workers have suggested that oxalic acid is not very effective. Therefore, the H-Hxl method is recommended for general exploration use. ?? 1982.

  3. Bioanalysis of underivatized amino acids in non-invasive exhaled breath condensate samples using liquid chromatography coupled with tandem mass spectrometry.

    Science.gov (United States)

    Konieczna, Lucyna; Pyszka, Magdalena; Okońska, Magdalena; Niedźwiecki, Maciej; Bączek, Tomasz

    2018-03-23

    Exhaled breath condensate (EBC) is receiving increased attention as a novel, entirely non-invasive technique for collecting biomarker samples. This increased attention is due to the fact that EBC is simple, effort independent, rapid, can be repeated frequently, and can be performed on young children and patients suffering from a variety of diseases. By having a subject breathe tidally through a cooling system for 15-20 min, a sufficient amount of condensate is collected for analysis of biomarkers in clinical studies. However, bioanalysis of EBC involves an unavoidable sample preparation step due to the low concentration of its components. Thus, there is a need for a new and more sensitive analytical method of assessing EBC samples. While researchers have considered analyses of single and small quantities of amino acids - for example, those connected with leukemia - no one has previously attempted to simultaneously analyze a panel of 23 amino acids. Moreover, the present study is well-justified, as prior studies focusing on single amino acids and leukemia at the moment of diagnosis and during chemotherapy (33 days of treatment) are inconsistent. In the present study, amino acids were separated using an XBridge Amide column (3 mm × 100 mm, 3.5 μm). The mobile phase consisted of 10 mM of ammonium buffer in water with a pH of 3 (Phase A) and 10 mM ammonium buffer in acetonitrile (Phase B) under gradient program elution. The analytes were detected in electrospray positive ionization mode. Under optimal conditions, the proposed method exhibited limits of quantification (LOQ) in the range of 0.05-0.5 ng/mL, and good linearity, with the determination coefficient (R 2 ) falling between 0.9904 and 0.9998. The accuracy in human exhaled breath condensate samples ranged between 93.3-113.3% for the 23 studied amino acids, with intra- and inter-day coefficient of variation (CVs) of 0.13-9.92% and 0.17-10.53%, respectively. To demonstrate the liquid

  4. Rapid Screening of Carboxylic Acids from Waste and Surface Waters by ESI-MS/MS Using Barium Ion Chemistry and On-Line Membrane Sampling

    Science.gov (United States)

    Duncan, Kyle D.; Volmer, Dietrich A.; Gill, Chris G.; Krogh, Erik T.

    2016-03-01

    Negative ion tandem mass spectrometric analysis of aliphatic carboxylic acids often yields only non-diagnostic ([M - H]-) ions with limited selective fragmentation. However, carboxylates cationized with Ba2+ have demonstrated efficient dissociation in positive ion mode, providing structurally diagnostic product ions. We report the application of barium adducts followed by collision induced dissociation (CID), to improve selectivity for rapid screening of carboxylic acids in complex aqueous samples. The quantitative MS/MS method presented utilizes common product ions of [M - H + Ba]+ precursor ions. The mechanism of product ion formation is investigated using isotopically labeled standards and a series of structurally related carboxylic acids. The results suggest that hydrogen atoms in the β and γ positions yield common product ions ([BaH]+ and [BaOH]+). Furthermore, the diagnostic product ion at m/z 196 serves as a qualifying ion for carboxylate species. This methodology has been successfully used in conjunction with condensed phase membrane introduction mass spectrometry (CP-MIMS), with barium acetate added directly to the methanol acceptor phase. The combination enables rapid screening of carboxylic acids directly from acidified water samples (wastewater effluent, spiked natural waters) using a capillary hollow fiber PDMS membrane immersion probe. We have applied this technique for the direct analysis of complex naphthenic acid mixtures spiked into natural surface waters using CP-MIMS. Selectivity at the ionization and tandem mass spectrometry level eliminate isobaric interferences from hydroxylated species present within the samples, which have been observed in negative electrospray ionization.

  5. Rapid Screening of Carboxylic Acids from Waste and Surface Waters by ESI-MS/MS Using Barium Ion Chemistry and On-Line Membrane Sampling.

    Science.gov (United States)

    Duncan, Kyle D; Volmer, Dietrich A; Gill, Chris G; Krogh, Erik T

    2016-03-01

    Negative ion tandem mass spectrometric analysis of aliphatic carboxylic acids often yields only non-diagnostic ([M - H](-)) ions with limited selective fragmentation. However, carboxylates cationized with Ba(2+) have demonstrated efficient dissociation in positive ion mode, providing structurally diagnostic product ions. We report the application of barium adducts followed by collision induced dissociation (CID), to improve selectivity for rapid screening of carboxylic acids in complex aqueous samples. The quantitative MS/MS method presented utilizes common product ions of [M - H + Ba](+) precursor ions. The mechanism of product ion formation is investigated using isotopically labeled standards and a series of structurally related carboxylic acids. The results suggest that hydrogen atoms in the β and γ positions yield common product ions ([BaH](+) and [BaOH](+)). Furthermore, the diagnostic product ion at m/z 196 serves as a qualifying ion for carboxylate species. This methodology has been successfully used in conjunction with condensed phase membrane introduction mass spectrometry (CP-MIMS), with barium acetate added directly to the methanol acceptor phase. The combination enables rapid screening of carboxylic acids directly from acidified water samples (wastewater effluent, spiked natural waters) using a capillary hollow fiber PDMS membrane immersion probe. We have applied this technique for the direct analysis of complex naphthenic acid mixtures spiked into natural surface waters using CP-MIMS. Selectivity at the ionization and tandem mass spectrometry level eliminate isobaric interferences from hydroxylated species present within the samples, which have been observed in negative electrospray ionization.

  6. Italian steam power plants

    Energy Technology Data Exchange (ETDEWEB)

    von Rautenkranz, J

    1939-01-01

    A brief history of geothermal power production in Italy is presented. Boric acid has been produced on an industrial scale since 1818. The first electrical power was generated in 1904, and by 1939 the output of geothermal power plants had reached 500 GWh, with major expansion of facilities planned.

  7. Germination and storage of pollen

    NARCIS (Netherlands)

    Visser, T.

    1955-01-01

    Germination of pear pollen markedly improved when boric acid was added to the medium. The pollen was more sensitive to boron in water than in 10 % sugar solution. Supplying weak solutions of boron to pear branches before flowering resulted in a good germination of the pollen in sugar solution

  8. Methods for separating boron from borated paraffin wax and its determination by ion chromatography

    International Nuclear Information System (INIS)

    Jeyakumar, S.

    2015-01-01

    Boron compounds are found to be useful in shielding against high-energy neutrons. In radiotherapy treatments, in order to protect occupational workers and patients from the undesirable neutron and gamma doses, paraffin wax containing B 4 C/boric acid is used. Low-level borate wastes generated from the nuclear power plants have been immobilized with paraffin wax using a concentrate waste drying system (CWDS). Borated paraffin waxes are prepared by mixing calculated amounts of either boric acid or boron carbide with the molten wax. This necessitates the determination of boron at different locations in order to check the homogeneous distribution of B over the borated wax. The determination of boron in nuclear materials is inevitable due to its high neutron absorption cross section. For the determination of boron in borated waxes, not many methods have been reported. A method based on the pyrohydrolysis extraction of boron and its quantification with ion chromatography was proposed for paraffin waxes borated with H 3 BO 3 and B 4 C. The B 4 C optimum pyrohydrolysis conditions were identified. Wax samples were mixed with U 3 O 8 , which prevents the sample from flare up, and also accelerates the extraction of boron. Pyrohydrolysis was carried out with moist O 2 at 950℃ for 60 and 90 min for wax with H 3 BO 3 and wax with B 4 C, respectively. Two simple methods of separation based on alkali extraction and melting wax in alkali were also developed exclusively for wax with H 3 BO 3 . In all the separations, the recovery of B was above 98%. During IC separation, B was separated as boron-mannitol anion complex. Linear calibration was obtained between 0.1 and 50 ppm of B, and LOD was calculated as 5 ppb (S/N=3). The reproducibility was better than 5% (RSD)

  9. Evaluation of acid leaching method for the determination of uranium in fecal samples from occupational workers at Tarapur

    International Nuclear Information System (INIS)

    Raveendran, Nanda; Dubla, Rupali; Yadav, J.R.; Rao, D.D.; Baburajan, A.

    2015-01-01

    Assessment of internal contamination due to inhalation, ingestion or injection of radionuclides to occupational workers is carried out by analysis of excreta samples and whole body counting. Routine monitoring of radiation workers for assessing actinides intake are done either by urine or fecal sample analysis. This paper deals with the evaluation of analytical method for the determination of isotopes of uranium in fecal samples submitted by occupational workers from operating plants at Tarapur. The method involves sample ashing, addition of 232 U tracer for radiochemical recovery and acid leaching preconcentration stage followed by anion exchange separation. Thirteen routine fecal samples submitted by radiation workers under their routine monitoring practices were collected and analyzed. Radiochemical tracer recovery was obtained in the range of 52% to 86.4 % with a mean and standard deviation of 64.7% and 12.3% respectively. (author)

  10. Nonlinear binding of phenanthrene to the extracted fulvic acid fraction in soil in comparison with other organic matter fractions and to the whole soil sample

    International Nuclear Information System (INIS)

    Liu Wenxin; Xu, Shanshan; Xing, Baoshan; Pan, Bo; Tao, Shu

    2010-01-01

    Fractions of soil organic matter in a natural soil were extracted and sorption (or binding) characteristics of phenanthrene on each fraction and to the whole sample were investigated. The organic carbon normalized single point sorption (or binding) coefficient followed lipid > humin (HM) > humic acid (HA) > fulvic acid (FA) > whole soil sample, while the nonlinear exponent exhibited lipid > FA > HA > whole soil sample > HM. FA showed nonlinear binding of phenanthrene as it often does with other fractions. HM and HA contributed the majority of organic carbon in the soil. The calculated sorption coefficients of the whole soil were about two times greater than the measured values at different equilibrium phenanthrene concentrations. As for phenanthrene, the sorption capacity and nonlinearity of the physically mixed HA-HM mixtures were stronger as compared to the chemically reconstituted HA-HM composite. This was attributed to (besides the conditioning effect of the organic solvents) interactions between HA and HM and acid-base additions during fractionation. - Nonlinear binding of phenanthrene to fulvic acid extracted from soil organic matter was found.

  11. Chemometric deconvolution of gas chromatographic unresolved conjugated linoleic acid isomers triplet in milk samples.

    Science.gov (United States)

    Blasko, Jaroslav; Kubinec, Róbert; Ostrovský, Ivan; Pavlíková, Eva; Krupcík, Ján; Soják, Ladislav

    2009-04-03

    A generally known problem of GC separation of trans-7;cis-9; cis-9,trans-11; and trans-8,cis-10 CLA (conjugated linoleic acid) isomers was studied by GC-MS on 100m capillary column coated with cyanopropyl silicone phase at isothermal column temperatures in a range of 140-170 degrees C. The resolution of these CLA isomers obtained at given conditions was not high enough for direct quantitative analysis, but it was, however, sufficient for the determination of their peak areas by commercial deconvolution software. Resolution factors of overlapped CLA isomers determined by the separation of a model CLA mixture prepared by mixing of a commercial CLA mixture and CLA isomer fraction obtained by the HPLC semi-preparative separation of milk fatty acids methyl esters were used to validate the deconvolution procedure. Developed deconvolution procedure allowed the determination of the content of studied CLA isomers in ewes' and cows' milk samples, where dominant isomer cis-9,trans-11 is eluted between two small isomers trans-7,cis-9 and trans-8,cis-10 (in the ratio up to 1:100).

  12. Differential pulse polarographic determination of trace antimony in standard biological samples after preconcentration using 2-nitroso-1-naphthol-4-sulfonic acid

    International Nuclear Information System (INIS)

    Taher, M. A.

    2003-01-01

    A highly selective, rapid and economical differential polarographic method has been developed for the determination of trace amounts of antimony in various standard alloys and biological samples after of its 2-naphthol-4 sulfonic acid tetradecyl dimethylbenzylammonium chloride on microcrystalline naphthalene in the ph range of 7.5-11.0. After filtration, the solid mass is shaken with 8-10 ml of 1 M hydrochloric acid (with preconcentration factor of 10) and antimony is determined by differential pulse polarography. Antimony can alternatively be quantitatively absorbed on 2-nitroso-1-naphthol-4-sulfonic acid tetradecyl dimethylbenzylammonium-naphthalene absorbed packed in a column (with preconcentration factor of 30) and determined similarly. In this case, 1.5 μg of antimony can be concentrated in a column from 300 ml of aqueous sample, where its concentration is as low as 5 ng/ml. Characterization of the electro active process included an examination of the degree of reversibility. The results show that the irreversibility of antimony. Various parameters such as the effect of ph, volume of aqueous phase, HCl concentration, reagent concentration, naphthalene concentration, shaking time and interference of a number of metal ions on the determination of antimony have been studied in detail to optimize the conditions for determination in standard alloys and standard biological samples

  13. Choice of infusion-sampling mode for tracer studies of free fatty acid metabolism

    International Nuclear Information System (INIS)

    Jensen, M.D.; Rogers, P.J.; Ellman, M.G.; Miles, J.M.

    1988-01-01

    To determine the preferred infusion-sampling mode for isotopic studies of free fatty acid (FFA) metabolism, tracer [( 14 C]palmitate) was infused into the left ventricle of five anesthetized dogs, and tracee ([ 3 H]palmitate) was infused into three separate peripheral veins of each dog. The [ 14 C]palmitate specific activity (SA) was lower in mixed venous than arterial blood, and [ 3 H]palmitate SA was equal in both sites. The actual infusion rate of [ 3 H]palmitate [2.15 +/- 0.31 X 10(5) disintegrations/min (dpm).kg-1.min-1] could be accurately predicted (2.14 +/- 0.32 X 10(5) dpm.kg-1.min-1) using the known [ 14 C]palmitate infusion rate and the arterial plasma [ 14 C]-to-[ 3 H]palmitate ratio. In contrast, the mixed venous [ 14 C]-to-[ 3 H]palmitate ratio resulted in overestimates (P less than 0.05) of the actual [ 3 H]palmitate infusion rate. In summary, venous tracer infusion with arterial blood sampling for FFA tracer studies provides the most accurate estimates of tracee rate of appearance

  14. Zinc corrosion after loss-of-coolant accidents in pressurized water reactors – Physicochemical effects

    Energy Technology Data Exchange (ETDEWEB)

    Kryk, Holger, E-mail: h.kryk@hzdr.de [Helmholtz-Zentrum Dresden-Rossendorf, Institute of Fluid Dynamics, P.O. Box 510119, D-01314 Dresden (Germany); Hoffmann, Wolfgang [Helmholtz-Zentrum Dresden-Rossendorf, Institute of Fluid Dynamics, P.O. Box 510119, D-01314 Dresden (Germany); Kästner, Wolfgang; Alt, Sören; Seeliger, André; Renger, Stefan [Hochschule Zittau/Görlitz, Institute of Process Technology, Process Automation and Measuring Technology, Theodor-Körner-Allee 16, D-02763 Zittau (Germany)

    2014-12-15

    Highlights: • Physicochemical effects due to post-LOCA zinc corrosion in PWR were elucidated. • Decreasing solubility of corrosion products with increasing temperature was found. • Solid corrosion products may be deposited on hot surfaces and/or within hot-spots. • Corrosion products precipitating from coolant were identified as zinc borates. • Depending on coolant temperature, different types of zinc borate are formed. - Abstract: Within the framework of the reactor safety research, generic experimental investigations were carried out aiming at the physicochemical background of possible zinc corrosion product formation, which may occur inside the reactor pressure vessel during the sump circulation operation after loss-of-coolant accidents in pressurized water reactors. The contact of the boric acid containing coolant with hot-dip galvanized steel containment internals causes corrosion of the corresponding materials resulting in dissolution of the zinc coat. A retrograde solubility of zinc corrosion products with increasing temperature was observed during batch experiments of zinc corrosion in boric acid containing coolants. Thus, the formation and deposition of solid corrosion products cannot be ruled out if the coolant containing dissolved zinc is heated up during its recirculation into hot regions within the emergency cooling circuit (e.g. hot-spots in the core). Corrosion experiments at a lab-scale test facility, which included formation of corrosion products at a single heated cladding tube, proved that dissolved zinc, formed at low temperatures in boric acid solution by zinc corrosion, turns into solid deposits of zinc borates when contacting heated zircaloy surfaces during the heating of the coolant. Moreover, the temperature of formation influences the chemical composition of the zinc borates and thus the deposition and mobilization behavior of the products.

  15. Zinc corrosion after loss-of-coolant accidents in pressurized water reactors – Physicochemical effects

    International Nuclear Information System (INIS)

    Kryk, Holger; Hoffmann, Wolfgang; Kästner, Wolfgang; Alt, Sören; Seeliger, André; Renger, Stefan

    2014-01-01

    Highlights: • Physicochemical effects due to post-LOCA zinc corrosion in PWR were elucidated. • Decreasing solubility of corrosion products with increasing temperature was found. • Solid corrosion products may be deposited on hot surfaces and/or within hot-spots. • Corrosion products precipitating from coolant were identified as zinc borates. • Depending on coolant temperature, different types of zinc borate are formed. - Abstract: Within the framework of the reactor safety research, generic experimental investigations were carried out aiming at the physicochemical background of possible zinc corrosion product formation, which may occur inside the reactor pressure vessel during the sump circulation operation after loss-of-coolant accidents in pressurized water reactors. The contact of the boric acid containing coolant with hot-dip galvanized steel containment internals causes corrosion of the corresponding materials resulting in dissolution of the zinc coat. A retrograde solubility of zinc corrosion products with increasing temperature was observed during batch experiments of zinc corrosion in boric acid containing coolants. Thus, the formation and deposition of solid corrosion products cannot be ruled out if the coolant containing dissolved zinc is heated up during its recirculation into hot regions within the emergency cooling circuit (e.g. hot-spots in the core). Corrosion experiments at a lab-scale test facility, which included formation of corrosion products at a single heated cladding tube, proved that dissolved zinc, formed at low temperatures in boric acid solution by zinc corrosion, turns into solid deposits of zinc borates when contacting heated zircaloy surfaces during the heating of the coolant. Moreover, the temperature of formation influences the chemical composition of the zinc borates and thus the deposition and mobilization behavior of the products

  16. Mercury analysis of acid- and alkaline-reduced biological samples: identification of meta-cinnabar as the major biotransformed compound in algae.

    Science.gov (United States)

    Kelly, David; Budd, Kenneth; Lefebvre, Daniel D

    2006-01-01

    The biotransformation of Hg(II) in pH-controlled and aerated algal cultures was investigated. Previous researchers have observed losses in Hg detection in vitro with the addition of cysteine under acid reduction conditions in the presence of SnCl2. They proposed that this was the effect of Hg-thiol complexing. The present study found that cysteine-Hg, protein and nonprotein thiol chelates, and nucleoside chelates of Hg were all fully detectable under acid reduction conditions without previous digestion. Furthermore, organic (R-Hg) mercury compounds could not be detected under either the acid or alkaline reduction conditions, and only beta-HgS was detected under alkaline and not under acid SnCl2 reduction conditions. The blue-green alga Limnothrix planctonica biotransformed the bulk of Hg(II) applied as HgCl2 into a form with the analytical properties of beta-HgS. Similar results were obtained for the eukaryotic alga Selenastrum minutum. No evidence for the synthesis of organomercurials such as CH3Hg+ was obtained from analysis of either airstream or biomass samples under the aerobic conditions of the study. An analytical procedure that involved both acid and alkaline reduction was developed. It provides the first selective method for the determination of beta-HgS in biological samples. Under aerobic conditions, Hg(II) is biotransformed mainly into beta-HgS (meta-cinnabar), and this occurs in both prokaryotic and eukaryotic algae. This has important implications with respect to identification of mercury species and cycling in aquatic habitats.

  17. Mercury Analysis of Acid- and Alkaline-Reduced Biological Samples: Identification of meta-Cinnabar as the Major Biotransformed Compound in Algae†

    Science.gov (United States)

    Kelly, David; Budd, Kenneth; Lefebvre, Daniel D.

    2006-01-01

    The biotransformation of HgII in pH-controlled and aerated algal cultures was investigated. Previous researchers have observed losses in Hg detection in vitro with the addition of cysteine under acid reduction conditions in the presence of SnCl2. They proposed that this was the effect of Hg-thiol complexing. The present study found that cysteine-Hg, protein and nonprotein thiol chelates, and nucleoside chelates of Hg were all fully detectable under acid reduction conditions without previous digestion. Furthermore, organic (R-Hg) mercury compounds could not be detected under either the acid or alkaline reduction conditions, and only β-HgS was detected under alkaline and not under acid SnCl2 reduction conditions. The blue-green alga Limnothrix planctonica biotransformed the bulk of HgII applied as HgCl2 into a form with the analytical properties of β-HgS. Similar results were obtained for the eukaryotic alga Selenastrum minutum. No evidence for the synthesis of organomercurials such as CH3Hg+ was obtained from analysis of either airstream or biomass samples under the aerobic conditions of the study. An analytical procedure that involved both acid and alkaline reduction was developed. It provides the first selective method for the determination of β-HgS in biological samples. Under aerobic conditions, HgII is biotransformed mainly into β-HgS (meta-cinnabar), and this occurs in both prokaryotic and eukaryotic algae. This has important implications with respect to identification of mercury species and cycling in aquatic habitats. PMID:16391065

  18. Comparison of Buffer Effect of Different Acids During Sandstone Acidizing

    International Nuclear Information System (INIS)

    Shafiq, Mian Umer; Mahmud, Hisham Khaled Ben; Hamid, Mohamed Ali

    2015-01-01

    The most important concern of sandstone matrix acidizing is to increase the formation permeability by removing the silica particles. To accomplish this, the mud acid (HF: HCl) has been utilized successfully for many years to stimulate the sandstone formations, but still it has many complexities. This paper presents the results of laboratory investigations of different acid combinations (HF: HCl, HF: H 3 PO 4 and HF: HCOOH). Hydrofluoric acid and fluoboric acid are used to dissolve clays and feldspar. Phosphoric and formic acids are added as a buffer to maintain the pH of the solution; also it allows the maximum penetration of acid into the core sample. Different tests have been performed on the core samples before and after the acidizing to do the comparative study on the buffer effect of these acids. The analysis consists of permeability, porosity, color change and pH value tests. There is more increase in permeability and porosity while less change in pH when phosphoric and formic acids were used compared to mud acid. From these results it has been found that the buffer effect of phosphoric acid and formic acid is better than hydrochloric acid. (paper)

  19. Lot quality assurance sampling of sputum acid-fast bacillus smears for assessing sputum smear microscopy centers.

    Science.gov (United States)

    Selvakumar, N; Murthy, B N; Prabhakaran, E; Sivagamasundari, S; Vasanthan, Samuel; Perumal, M; Govindaraju, R; Chauhan, L S; Wares, Fraser; Santha, T; Narayanan, P R

    2005-02-01

    Assessment of 12 microscopy centers in a tuberculosis unit by blinded checking of eight sputum smears selected by using a lot quality assurance sampling (LQAS) method and by unblinded checking of all positive and five negative slides, among the slides examined in a month in a microscopy centre, revealed that the LQAS method can be implemented in the field to monitor the performance of acid-fast bacillus microscopy centers in national tuberculosis control programs.

  20. Determination of uranium in urine samples for workers in the phosphoric acid purification using fluorimetry technique

    International Nuclear Information System (INIS)

    Kharita, M. H.; Sakhita, Kh.; Aldalal, Z.

    2003-10-01

    There is probability of exposure to uranium for workers in the phosphoric acid purification (internal exposure) by inhalation, and the deposition of this uranium in organs and tissues, and the consequence excreation out of the body by perspiration or urine. This study focuses on the determination of uranium in urine samples of workers. All results seem to be under the detection limit of the method, therefore no routine monitoring is required. (author)

  1. Determination of boron distribution in rat's brain, kidney and liver

    Energy Technology Data Exchange (ETDEWEB)

    Pazirandeh, Ali [Nuclear Engineering Department, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Science and Technology Research Center, AEOI, Tehran (Iran, Islamic Republic of)], E-mail: paziran@khayam.ut.ac.ir; Jameie, Behnam [Neuroscience Lab, Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Zargar, Maysam [Nuclear Engineering Department, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of)

    2009-07-15

    To determine relative boron distribution in rat's brain, liver and kidney, a mixture of boric acid and borax, was used. After transcardial injection of the solution, the animals were sacrificed and the brain, kidney and liver were removed. The coronal sections of certain areas of the brain were prepared by freezing microtome. The slices were sandwiched within two pieces of CR-39. The samples were bombarded in a thermal neutron field of the TRR pneumatic facility. The alpha tracks are registered on CR-39 after being etched in NaOH. The boron distribution was determined by counting these alpha tracks CR-39 plastics. The distribution showed non-uniformity in brain, liver and kidney.

  2. Investigation of surface and underground waters about the Blayais nuclear site - 2010

    International Nuclear Information System (INIS)

    Migeon, A.; Bernollin, A.; Dunand, E.; Barbey, P.; Boilley, D.; Josset, M.

    2011-01-01

    This investigation aims at proposing a first assessment of the impact of releases on surface and underground waters around the Blayais nuclear power station, i.e. the assessment of the (mainly radiological) quality of waters. The report identifies the various pollution sources: old sources (like atmospheric nuclear tests, nuclear accidents), incidents in the Blayais station, and potential sources for the present contamination. Different radionuclides are searched like tritium, carbon 14, gamma radioactivity (from different elements), some beta emitters, radon as well as some chemicals related to the station activity (hydrazine, boric acid, EDTA, lithium, morpholine). Sampling sites are presented (estuary, canals, reservoirs). Radiological and chemical analysis are reported and commented. Significant presence of Tritium and Nickel-63 are noticed

  3. Experimental Investigation on the Effects of Coolant Concentration on Sub-Cooled Boiling and Crud Deposition on Reactor Cladding at Prototypical PWR Operating Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Schultis, J., Kenneth; Fenton, Donald, L.

    2006-10-20

    Increasing demand for energy necessitates nuclear power units to increase power limits. This implies significant changes in the design of the core of the nuclear power units, therefore providing better performance and safety in operations. A major hindrance to the increase of nuclear reactor performance especially in Pressurized Deionized water Reactors (PWR) is Axial Offset Anomaly (AOA)--the unexpected change in the core axial power distribution during operation from the predicted distribution. This problem is thought to be occur because of precipitation and deposition of lithiated compounds like boric acid (H{sub 2}BO{sub 3}) and lithium metaborate (LiBO{sub 2}) on the fuel rod cladding. Deposited boron absorbs neutrons thereby affecting the total power distribution inside the reactor. AOA is thought to occur when there is sufficient build-up of crud deposits on the cladding during subcooled nucleate boiling. Predicting AOA is difficult as there is very little information regarding the heat and mass transfer during subcooled nucleate boiling. An experimental investigation was conducted to study the heat transfer characteristics during subcooled nucleate boiling at prototypical PWR conditions. Pool boiling tests were conducted with varying concentrations of lithium metaborate (LiBO{sub 2}) and boric acid (H{sub 2}BO{sub 3}) solutions in deionized water. The experimental data collected includes the effect of coolant concentration, subcooling, system pressure and heat flux on pool the boiling heat transfer coefficient. The analysis of particulate deposits formed on the fuel cladding surface during subcooled nucleate boiling was also performed. The results indicate that the pool boiling heat transfer coefficient degrades in the presence of boric acid and lithium metaborate compared to pure deionized water due to lesser nucleation. The pool boiling heat transfer coefficients decreased by about 24% for 5000 ppm concentrated boric acid solution and by 27% for 5000 ppm

  4. Comparative antibacterial activity of topical antiseptic eardrops against methicillin-resistant Staphylococcus aureus and quinolone-resistant Pseudomonas aeruginosa.

    Science.gov (United States)

    Youn, Cha Kyung; Jang, Sook-Jin; Jo, Eu-Ri; Choi, Ji Ae; Sim, Ju-Hwan; Cho, Sung Il

    2016-06-01

    Aural irrigation using antiseptic solutions can be an effective medical treatment of chronic suppurative otitis media (CSOM) owing to the increasing prevalence of antibiotic-resistant CSOM infections. In the present study, we compared the antimicrobial activities of 100% Burow's solution, 50% Burow's solution, 2% acetic acid, vinegar with water (1:1), and 4% boric acid solution against methicillin-resistant Staphylococcus aureus (MRSA), methicillin-susceptible S. aureus (MSSA), quinolone-resistant Pseudomonas aeruginosa (QRPA), and quinolone-susceptible P. aeruginosa (QSPA) in vitro. We examined the antimicrobial activities of five antiseptic solutions against MRSA, MSSA, QRPA, and QSPA. The antimicrobial activities of the solutions were calculated as a percentage of the surviving microorganisms by dividing the viable count in each antiseptic solution with that in control. The time (D10 value) required for each of the five solutions to inactivate 90% of the microorganism population was also investigated. Burow's solution exhibited the highest antimicrobial activity and the lowest D10 value against MRSA, MSSA, QRPA, and QSPA, followed by 2% acetic acid, vinegar with water (1:1), and 4% boric acid solution. Our results indicate that Burow's solution has the most potent activity against bacteria including antibiotic-resistant strains. Twofold dilution of the solution is recommended to avoid ototoxicity. Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

  5. Microwave synthesis of homogeneous and highly luminescent BCNO nanoparticles for the light emitting polymer materials

    Energy Technology Data Exchange (ETDEWEB)

    Iwasaki, Hideharu [Battery Materials Laboratory, Kurashiki Research Center, Kuraray Co., Ltd., 2045-1, Sakazu, Kurashiki, Okayama 710-0801 (Japan); Department of Chemical Engineering, Graduate School of Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi Hiroshima 739 8527 (Japan); Ogi, Takashi, E-mail: ogit@hiroshima-u.ac.jp [Department of Chemical Engineering, Graduate School of Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi Hiroshima 739 8527 (Japan); Iskandar, Ferry [Department of Physics, Institute of Technology Bandung, Ganesha 10, Bandung 40132, West Java (Indonesia); Aishima, Kana; Okuyama, Kikuo [Department of Chemical Engineering, Graduate School of Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi Hiroshima 739 8527 (Japan)

    2015-10-15

    Nano-sized boron carbon oxynitride (BCNO) phosphors around 50 nm containing no rare earth metal and free from color heterogeneity were synthesized from mixtures of boric acid, urea, and citric acid by microwave heating with substantially shorter reaction times and lower temperatures than in the conventional BCNO preparation method such as electric-furnace heating. The emission wavelength of the phosphors varied with the mixing ratio of raw materials and it was found that lowering the proportion of urea to boric acid or citric acid tended to increase the internal quantum yield and shorten the emission wavelength under excitation at 365 nm. It was also found for the first time that a light-emitting polymer could be synthesized from a mixture of the prepared BCNO nanoparticles and a polyvinyl alcohol. This polymer composite exhibited uniform dispersion and stabilization of the luminescence and had a high internal quantum yield of 54%, which was higher than that of the phosphor alone. - Highlights: • Nano-sized BCNO phosphor was synthesized via microwave heating. • BCNO nanophosphor has homogeneous and high luminescence. • Emission wavelength was tunable by changing the ratio of precursor components. • BCNO nanophosphor can be easily dispersed in a polyvinyl alcohol. • BCNO–polymer composite exhibited uniform high internal quantum yield.

  6. Characterization of the first core sample of neutralized current acid waste from double-shell tank 101-AZ

    International Nuclear Information System (INIS)

    Peterson, M.E.; Scheele, R.D.; Tingey, J.M.

    1989-09-01

    In FY 1989, Westinghouse Hanford Company (WHC) successfully obtained four core samples (totaling seven segments) of neutralized current acid waste (NCAW) from double-shell tanks (DSTs) 101-AZ and 102-AZ. A segment was a 19-in.-long and 1-in.-diameter cylindrical sample of waste. A core sample consisted of enough 19-in.-long segments to obtain the waste of interest. Three core samples were obtained from DST 101-AZ and one core sample from DST 102-AZ. Two DST 101-AZ core samples consisted of two segments per core, and the third core sample consisted of only one segment. The third core consisted of the solids from the bottom of the tank and was used to determine the relative abrasiveness of this NCAW. The DST 102-AZ core sample consisted of two segments. The core samples were transported to the Pacific Northwest Laboratory (PNL), where the waste was extruded from its sampler and extensively characterized. A characterization plan was followed that simulated the processing of the NCAW samples through retrieval, pretreatment and vitrification process steps. Physical, rheological, chemical and radiochemical properties were measured throughout the process steps. The characterization of the first core sample from DST 101-AZ was completed, and the results are provided in this report. The results for the other core characterizations will be reported in future reports. 3 refs., 13 figs., 10 tabs

  7. Effect of boron and phosphate compounds on physical, mechanical, and fire properties of wood-polypropylene composites

    Science.gov (United States)

    Nadir Ayrilmis; Turgay Akbulut; Turker Dundar; Robert H. White; Fatih Mengeloglu; Umit Buyuksari; Zeki Candan; Erkan Avci

    2012-01-01

    Physical, mechanical, and fire properties of the injection-molded wood flour/polypropylene composites incorporated with different contents of boron compounds; borax/boric acid and zinc borate, and phosphate compounds; mono and diammonium phosphates were investigated. The effect of the coupling agent content, maleic anhydride-grafted polypropylene, on the properties of...

  8. Sensitive Electrochemical Determination of Gallic Acid: Application in Estimation of Total Polyphenols in Plant Samples

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Sheikh-Mohseni

    2016-12-01

    Full Text Available A modified electrode was prepared by modification of the carbon paste electrode (CPE with graphene nano-sheets. The fabricated modified electrode exhibited an electrocatalytic activity toward gallic acid (GA oxidation because of good conductivity, low electron transfer resistance and catalytic effect. The graphene modified CPE had a lower overvoltage and enhanced electrical current respect to the bare CPE for the oxidation of GA. The oxidation potential of GA decreased more than 210 mV by the modified electrode. The modified electrode responded to the GA in the concentration range of 3.0 × 10-5-1.5 × 10-4 M with high sensitivity by the technique of differential pulse voltammetry. Also, detection limit of 1.1 × 10-7 M was obtained by this modified electrode for GA. This electrode was used for the successful determination of GA in plant samples. Therefore, the content of total polyphenols in plant samples can be determined by the proposed modified electrode based on the concentration of GA in the sample.

  9. The use of electrothermal vaporizer coupled to the inductively coupled plasma mass spectrometry for the determination of arsenic, selenium and transition metals in biological samples treated with formic acid

    Energy Technology Data Exchange (ETDEWEB)

    Tormen, Luciano, E-mail: lucianotormen@hotmail.com [Departamento de Quimica, Universidade Federal de Santa Catarina, Depto. Quimica, Campus Trindade, 88040-900 Florianopolis, SC (Brazil); Universidade Federal da Fronteira Sul - UFFS, Campus Laranjeiras do Sul, 85303-775 Laranjeiras do Sul, PR (Brazil); Gil, Raul A. [Instituto de Quimica de San Luis (UNSL-CONICET), Chacabuco y Pedernera, D5700BWQ San Luis (Argentina); Frescura, Vera L.A. [Departamento de Quimica, Universidade Federal de Santa Catarina, Depto. Quimica, Campus Trindade, 88040-900 Florianopolis, SC (Brazil); Martinez, Luis Dante [Instituto de Quimica de San Luis (UNSL-CONICET), Chacabuco y Pedernera, D5700BWQ San Luis (Argentina); Curtius, Adilson J. [Departamento de Quimica, Universidade Federal de Santa Catarina, Depto. Quimica, Campus Trindade, 88040-900 Florianopolis, SC (Brazil)

    2012-03-02

    Highlights: Black-Right-Pointing-Pointer Simple sample treatment of biologic samples with formic acid is proposed. Black-Right-Pointing-Pointer The treatment with formic acid is easy, rapid, less expensive and environmental friendly allowing a high sample throughput. Black-Right-Pointing-Pointer External calibration with aqueous standard allows the simultaneous determination of As, Co, Cu, Fe, Mn, Ni, Se and V. Black-Right-Pointing-Pointer The use of ETV avoids plasma instability, carbon deposit on the cones and does not require sample digestion. - Abstract: A fast method for the determination of As, Co, Cu, Fe, Mn, Ni, Se and V in biological samples by ETV-ICP-MS, after a simple sample treatment with formic acid, is proposed. Approximately 75 mg of each sample is mixed with 5 mL of formic acid, kept at 90 Degree-Sign C for 1 h and then diluted with nitric acid aqueous solution to a 5% (v/v) formic acid and 1% (v/v) nitric acid final concentrations. A palladium solution was used as a chemical modifier. The instrumental conditions, such as carrier gas flow rate, RF power, pyrolysis and vaporization temperatures and argon internal flow rate during vaporization were optimized. The formic acid causes a slight decrease of the analytes signal intensities, but does not increase the signal of the mainly polyatomic ions ({sup 14}N{sup 35}Cl{sup +}, {sup 14}N{sup 12}C{sup +}, {sup 40}Ar{sup 12}C{sup +}, {sup 13}C{sup 37}Cl{sup +}, {sup 40}Ar{sup 36}Ar{sup +}, {sup 40}Ar{sup 35}Cl{sup +}, {sup 35}Cl{sup 16}O{sup +}, {sup 40}Ar{sup 18}O{sup +}) that affect the analytes signals. The effect of charge transfer reactions, that could increase the ionization efficiency of some elements with high ionization potentials was not observed due to the elimination of most of the organic compounds during the pyrolysis step. External calibration with aqueous standard solutions containing 5% (v/v) formic acid allows the simultaneous determination of all analytes with high accuracy. The

  10. Efeitos da aplicação de reguladores vegetais e do ácido bórico, em estacas de lichieira (Litchi chinensis Sonn. Effects of growth regulators and boric acid on lychee (Litchi chinensis Sonn. cuttings

    Directory of Open Access Journals (Sweden)

    S. Leonel

    1993-05-01

    Full Text Available Estudaram-se as interações entre os ácidos indol-butírico, alfa-naftaleno-acético e bórico no desenvolvimento de calos e na sobrevivência das estacas de lichieira (Litchi chinensis Sonn.. As estacas apresentavam 25 cm de comprimento e 4 folhas cortadas pela metade, sendo retiradas em duas épocas diferentes (janeiro e abril e colocadas para enraizar em bandejas de isopor, tendo como substrato vermiculita e em condições de câmara de nebulização. Foi feita imersão de 2,5 cm da base das estacas, em soluções aquosas por l minuto. Os tratamentos utilizados corresponderam a 5.000 e 2.000 ppm de IBA; 3.000 e 1.500 ppra de NAA; 150 microgramas/ml de H3BO3; IBA 5.000 e 2.000 ppm + H3BO(3150 microgramas/ml; NAA 3.000 e 1.500 ppm + H3BO3 150 microgramas/ml e H2O. Avaliou-se a formação de calos e a sobrevivência das estacas após 120 dias do plantio. Através dos resultados obtidos, foi possível concluir que dos tratamentos utilizados, nenhum foi efetivo na formação de raízes, havendo somente a formação de calos. A melhor época para a retirada de estacas correspondeu ao mês de abril.Interactions between indolebutyric, naphtalen acetic and boric acids were studied on "callus" development and survival in lychee (Litchi chinensis Sonn. cuttings. The cuttings were twenty five cm long with four leaves cut in half and taken in two different periods (January and April Styrofoam trays, with vermiculite as substratum kept under intermittent mist were used as rooting media. Cuttings were imersed up to 2.5 cm from the base in water solutions, for one minute. The treatments were: 5,000 and 2,000 ppm of IBA; 3,000 and 1,500 ppm of NAA; 150 micrograms/ml H3BO3; IBA 5,000 and 2,000 ppm plus H3BO3 150 micrograms/ml; NAA 3,000 and 1,500 ppm plus boron 150 micrograms/ml and II2O. "Callus" formation and cutting survival were evaluated 120 days after planting. It was concluded that no treatments were effective on root formation, however, "callus

  11. The effect of the boron source composition ratio on the adsorption performance of hexagonal boron nitride without a template

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Ning, E-mail: zhangning5832@163.com; Zhang, Tong; Kan, Hongmin; Wang, Xiaoyang; Long, Haibo; Cui, Xingyu

    2015-08-01

    An inexpensive boric acid (H{sub 3}BO{sub 3}) and borax (Na{sub 2}B{sub 4}O{sub 7}·10H{sub 2}O) mix was used as a source of boron with different composition ratios, and urea was used as a nitrogen source, in flowing ammonia atmosphere, for the preparation of hexagonal boron nitride (h-BN) with different micro-morphologies. Under a certain synthesis process, the effects of the molar ratio of borax and boric acid (or simply the boron source composition ratio for short) on the phase composition of the sample were studied; the work also explored the effect of boron source composition ratio on the micro-morphology, adsorption desorption isotherm and specific surface area of the h-BN powder. The main purpose of this work was to determine the optimum composition ratio of preparing spherical mesoporous h-BN and ensure that the micro-mechanism underpinning the formation of spherical mesoporous h-BN was understood. The results showed that at the optimum boron source composition ratio of 1:1, globular mesoporous spheres with a diameter of approximately 600–800 nm could be obtained with the highest pore volume and specific surface area (230.2 m{sup 2}/g). - Graphical abstract: Display Omitted - Highlights: • Spherical h-BN was synthesized by controlling the boron source composition ratio. • Without extra spherical template, solid Na{sub 2}O was equal to a spherical template. • At boron source composition ratio of 1:1, h-BN had best adsorption performance.

  12. Retrospective bioindication of stratospheric ozone and ultraviolet radiation using hydroxycinnamic acid derivatives of herbarium samples of an aquatic liverwort.

    Science.gov (United States)

    Otero, Saúl; Núñez-Olivera, Encarnación; Martínez-Abaigar, Javier; Tomás, Rafael; Huttunen, Satu

    2009-01-01

    We analyzed bulk UV absorbance of methanolic extracts and levels of five UV-absorbing compounds (hydroxycinnamic acid derivatives) in 135 herbarium samples of the liverwort Jungermannia exsertifolia subsp. cordifolia from northern Europe. Samples had been collected in 1850-2006 (96% in June-August). Both UV absorbance and compound levels were correlated positively with collection year. p-Coumaroylmalic acid (C1) was the only compound showing a significant (and negative) correlation with stratospheric ozone and UV irradiance in the period that real data of these variables existed. Stratospheric ozone reconstruction (1850-2006) based on C1 showed higher values in June than in July and August, which coincides with the normal monthly variation of ozone. Combining all the data, there was no long-term temporal trend from 1850 to 2006. Reconstructed UV showed higher values in June-July than in August, but again no temporal trend was detected in 1918-2006 using the joint data. This agrees with previous UV reconstructions.

  13. Electrocatalytic simultaneous determination of ascorbic acid, uric acid and L-Cysteine in real samples using quercetin silver nanoparticles-graphene nanosheets modified glassy carbon electrode

    Science.gov (United States)

    Zare, Hamid R.; Jahangiri-Dehaghani, Fahime; Shekari, Zahra; Benvidi, Ali

    2016-07-01

    By immobilizing of quercetin at the surface of a glassy carbon electrode modified with silver nanoparticles and graphene nanosheets (Q-AgNPs-GNs-GCE) a new sensor has been fabricated. The cyclic voltammogram of Q-AgNPs-GNs-GCE shows a stable redox couple with surface confined characteristics. Q-AgNPs-GNs-GCE demonstrated a high catalytic activity for L-Cysteine (L-Cys) oxidation. Results indicated that L-Cys peak potential at Q-AgNPs-GNs-GCE shifted to less positive values compared to GNs-GCE or AgNPs-GCE. Also, the kinetic parameters such as the electron transfer coefficient,, and the heterogeneous electron transfer rate constant, k‧, for the oxidation of L-Cys at the Q-AgNPs-GNs-GCE surface were estimated. In differential pulse voltammetric determination, the detection limit of L-Cys was obtained 0.28 μM, and the calibration plots were linear within two ranges of 0.9-12.4 μM and 12.4-538.5 μM of L-Cys. Also, the proposed modified electrode is used for the simultaneous determinations of ascorbic acid (AA), uric acid (UA), and L-Cys. Finally, this study has demonstrated the practical analytical utility of the sensor for determination of AA in vitamin C tablet, L-Cys in a milk sample and UA in a human urine sample.

  14. Direct monitoring by carbon-13 nuclear magnetic resonance spectroscopy of the metabolism and metabolic rate of 13C-labeled compounds in vivo.

    Science.gov (United States)

    Iida, K; Hidoh, O; Fukami, J; Kajiwara, M

    1991-01-01

    Carbon-13 nuclear magnetic resonance spectroscopy has been used to observe the transformations of [1-13C]-D-glucose to [1,1'-13C2]-D-trehalose, and [3-13C]-L-alanine to [2-13C]-L-glutamic acid in the living body of Gryllodes sigillatus. [3-13C]-D-Alanine was not metabolized. The metabolic rate of [1-13C]-D-glucose was found to be altered by prior injection of boric acid.

  15. Acquisition of Heat Stable Enzymes from Thermophilic Microorganisms: Peroxidases, Ureases, and Glucose Oxidases.

    Science.gov (United States)

    1992-04-01

    heptahydrate, 1.50 g/L boric acid, 0.05 g/L copper sulfate pentahydrate . 0.20 g/L molybdic acid dihydrate sodium salt and 0.05 g/L cobalt chloride...vanadium, cobalt, magnesium, potassium, zinc, copper , manganese, sodium, chloride and various forms of nitrogen. In addition to pH and temperature...growth may not coincide with the optimal conditions for production of the desired enzyme. For isolate #135, the sulfate , magnesium, potassium and

  16. Boron and Coumaphos Residues in Hive Materials Following Treatments for the Control of Aethina tumida Murray.

    Directory of Open Access Journals (Sweden)

    Cesar Valdovinos-Flores

    Full Text Available In the search of alternatives for controlling Aethina tumida Murray, we recently proposed the BAA trap which uses boric acid and an attractant which mimics the process of fermentation caused by Kodamaea ohmeri in the hive. This yeast is excreted in the feces of A. tumida causing the fermentation of pollen and honey of infested hives and releasing compounds that function as aggregation pheromones to A. tumida. Since the boron is the toxic element in boric acid, the aim of this article is to assess the amount of boron residues in honey and beeswax from hives treated with the BAA trap. For this aim, the amount of bioaccumulated boron in products of untreated hives was first determined and then compared with the amount of boron of products from hives treated with the BAA trap in two distinct climatic and soil conditions. The study was conducted in the cities of Padilla, Tamaulipas, and Valladolid, Yucatan (Mexico from August 2014 to March 2015. The quantity of boron in honey was significantly less in Yucatan than in Tamaulipas; this agrees with the boron deficiency among Luvisol and Leptosol soils found in Yucatan compared to the Vertisol soil found in Tamaulipas. In fact, the honey from Yucatan has lower boron levels than those reported in the literature. The BAA treatment was applied for four months, results show that the BAA trap does not have any residual effect in either honey or wax; i.e., there is no significant difference in boron content before and after treatment. On the other hand, the organophosphate pesticide coumaphos was found in 100% of wax samples and in 64% of honey samples collected from Yucatan. The concentration of coumaphos in honey ranges from 0.005 to 0.040 mg/kg, which are below Maximum Residue Limit (MRL allowed in the European Union (0.1 mg/kg but 7.14% of samples exceeded the MRL allowed in Canada (0.02 mg/kg.

  17. Boron and Coumaphos Residues in Hive Materials Following Treatments for the Control of Aethina tumida Murray

    Science.gov (United States)

    Valdovinos-Flores, Cesar; Gaspar-Ramírez, Octavio; Heras–Ramírez, María Elena; Dorantes-Ugalde, José Antonio; Saldaña-Loza, Luz María

    2016-01-01

    In the search of alternatives for controlling Aethina tumida Murray, we recently proposed the BAA trap which uses boric acid and an attractant which mimics the process of fermentation caused by Kodamaea ohmeri in the hive. This yeast is excreted in the feces of A. tumida causing the fermentation of pollen and honey of infested hives and releasing compounds that function as aggregation pheromones to A. tumida. Since the boron is the toxic element in boric acid, the aim of this article is to assess the amount of boron residues in honey and beeswax from hives treated with the BAA trap. For this aim, the amount of bioaccumulated boron in products of untreated hives was first determined and then compared with the amount of boron of products from hives treated with the BAA trap in two distinct climatic and soil conditions. The study was conducted in the cities of Padilla, Tamaulipas, and Valladolid, Yucatan (Mexico) from August 2014 to March 2015. The quantity of boron in honey was significantly less in Yucatan than in Tamaulipas; this agrees with the boron deficiency among Luvisol and Leptosol soils found in Yucatan compared to the Vertisol soil found in Tamaulipas. In fact, the honey from Yucatan has lower boron levels than those reported in the literature. The BAA treatment was applied for four months, results show that the BAA trap does not have any residual effect in either honey or wax; i.e., there is no significant difference in boron content before and after treatment. On the other hand, the organophosphate pesticide coumaphos was found in 100% of wax samples and in 64% of honey samples collected from Yucatan. The concentration of coumaphos in honey ranges from 0.005 to 0.040 mg/kg, which are below Maximum Residue Limit (MRL) allowed in the European Union (0.1 mg/kg) but 7.14% of samples exceeded the MRL allowed in Canada (0.02 mg/kg). PMID:27092938

  18. Characterization of Zircaloy-2 and Zircaloy-4 by X-Ray fluorescence

    International Nuclear Information System (INIS)

    Sato, I.M.; Imakuma, K.; Salvador, V.L.R.

    1981-03-01

    The analytical characterization of zircaloy-2 and zircaloy-4 is intimataly connected with the determination of Sn, Fe, Cr, Ni, O, N, H, and Hf. An analytical method developed in this laboratory is discribed for the determination of metallic elements like Sn, Fe, Cr and Ni using the technique of X-ray fluorescence. The samples are prepared in the form of double-layer pellets using boric acid as a binding agent. The zircaloy-4 is dissolved in hydrofluoric acid and the metallic elements are converted to fluorides. The standard samples used for calibration are prepared from synthetic materials. The elements are determined by measuring the characteristic first order K α lines. A Zircaloy-4 sample analysed yielded the following values: Sn=1.30+-0.03%, Fe=0.18+-0.01%, Cr=0.088+-0.004% and Ni=14+-3 ppm. The reproducibility, precision, as well as the theoretical limit of detection of the method are discussed. The determination of the elements O, N and H present as occluded gas in the zircaloy is nearing completion. These analyses are being carried out by a Mass Spectrometric technique where an aliquot of the released gas is analysed. (Author) [pt

  19. Physical, mechanical, and fire properties of oriented strandboard with fire retardant treated veneers

    Science.gov (United States)

    Nadir Ayrilmis; Zeki Candan; Robert White

    2007-01-01

    This study evaluated physical, mechanical and fire properties of oriented strand boards (OSB) covered with fire retardant treated veneers. The beech (Fagus orientalis Lipsky) veneers were treated with either monoammonium phosphate, diammonium phosphate, lime water or a borax/boric acid (1 : 1 by weight) mixture. Physical and mechanical properties of the specimens were...

  20. Journal of Chemical Sciences | Indian Academy of Sciences

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences. G N Mukherjee. Articles written in Journal of Chemical Sciences. Volume 114 Issue 3 June 2002 pp 163-174 Inorganic and Analytical. Mixed ligand complex formation of Fe with boric acid and typical N-donor multidentate ligands · G N Mukherjee Ansuman Das · More Details ...

  1. Ultra low and negative expansion glass–ceramic materials ...

    Indian Academy of Sciences (India)

    Ultra low and negative expansion glass–ceramic materials have been obtained from pyrophyllite and blast furnace slag. The batch composition was modified with the addition of lithium carbonate, hydrated alumina, boric acid and nucleating agent (titania). The batch was melted at 1400°C followed by casting in the form of ...

  2. Ammonia role in WWER primary circuit water chemistry optimization

    International Nuclear Information System (INIS)

    Kritskij, V.G.; Stjagkin, P.S.; Chvedova, M.N.; Slobodov, A.A.

    1999-01-01

    Ammonia influence on iron crud's solubility at 300 deg. C and different relations of boric acid and alkaline cation sum are considered. Reduction of dose rate on WWER-440 steam generators at average ammonia concentration increasing is empirically explained. Practical recommendations on optimization of WWER primary circuit water chemistry are given. (author)

  3. Computer modeling of homogenization of boric acid in IRIS pressurizer

    International Nuclear Information System (INIS)

    Rives Sanz, Ronny; Montesinos Otero, Maria Elena; Gonzalez Mantecon, Javier

    2015-01-01

    Integral layout of nuclear reactor IRIS makes possible the elimination of the spray system; which is usually used to mitigate in-surge transient and help to boron homogenization. The study of transients with deficiencies in the boron homogenization in this technology is very important, because they can cause disturbances in the reactor power and insert a strong reactivity in the core. The aim of the present research is to model the IRIS pressurizer using the CFX code searching for designs alternatives that guaranteed its intrinsic security, focused on the phenomena before mentioned. A symmetric tri dimensional model equivalent to 1/8 of the total geometry was adopted to reduce mesh size and minimize processing time. The relationships are programmed and incorporated into the code. This paper discusses the model developed and the behavior of the system for representative transients sequences. The results of the analyzed IRIS transients could be applied to the design of the pressurizer internal structures and components. (Author)

  4. The Effect of Particle Size of Wollastonite Filler on Thermal Performance of Intumescent Fire Retardant Coating

    Directory of Open Access Journals (Sweden)

    Zia-ul-Mustafa M.

    2014-07-01

    Full Text Available Intumescent Fire retardant coatings (IFRC’s are one of the simplest ways to protect substrates exposed to fire. In this study, Wollastonite (W filler of two different particle sizes were used to determine the fire performance of intumescent fire retardant coating. The basic ingredients of the coating were ammonium poly-phosphate (APP as acid source, expandable graphite (EG as carbon source, melamine (MEL as blowing agent in epoxy binder, boric acid as additive and hardener as curing agent. A series of coating formulations were developed by using different weight percentages of both sized Wollastonite fillers. The coated steel substrate samples were tested for fire performance using Bunsen burner and char expansion was measured using furnace fire test. A Comparison of the coatings thermal performance was determined. Wollastonite containing filler particle size 10 μm showed better thermal performance than formulations containing filler’s particle size 44 μm.

  5. Collecting Samples for Testing

    Science.gov (United States)

    ... Creatinine Ratio Valproic Acid Vancomycin Vanillylmandelic Acid (VMA) VAP Vitamin A Vitamin B12 and Folate Vitamin D ... that used for CSF in that they require aspiration of a sample of the fluid through a ...

  6. An analytical method for trifluoroacetic Acid in water and air samples using headspace gas chromatographic determination of the methyl ester.

    Science.gov (United States)

    Zehavi, D; Seiber, J N

    1996-10-01

    An analytical method has been developed for the determination of trace levels of trifluoroacetic acid (TFA), an atmospheric breakdown product of several of the hydrofluorocarbon (HFC) and hydrochlorofluorocarbon (HCFC) replacements for the chlorofluorocarbon (CFC) refrigerants, in water and air. TFA is derivatized to the volatile methyl trifluoroacetate (MTFA) and determined by automated headspace gas chromatography (HSGC) with electron-capture detection or manual HSGC using GC/MS in the selected ion monitoring (SIM) mode. The method is based on the reaction of an aqueous sample containing TFA with dimethyl sulfate (DMS) in concentrated sulfuric acid in a sealed headspace vial under conditions favoring distribution of MTFA to the vapor phase. Water samples are prepared by evaporative concentration, during which TFA is retained as the anion, followed by extraction with diethyl ether of the acidified sample and then back-extraction of TFA (as the anion) in aqueous bicarbonate solution. The extraction step is required for samples with a relatively high background of other salts and organic materials. Air samples are collected in sodium bicarbonate-glycerin-coated glass denuder tubes and prepared by rinsing the denuder contents with water to form an aqueous sample for derivatization and analysis. Recoveries of TFA from spiked water, with and without evaporative concentration, and from spiked air were quantitative, with estimated detection limits of 10 ng/mL (unconcentrated) and 25 pg/mL (concentrated 250 mL:1 mL) for water and 1 ng/m(3) (72 h at 5 L/min) for air. Several environmental air, fogwater, rainwater, and surface water samples were successfully analyzed; many showed the presence of TFA.

  7. Application of a simple column-switching ion chromatography technique for removal of matrix interferences and sensitive fluorescence determination of acidic compounds (pharmaceutical drugs) in complex samples.

    Science.gov (United States)

    Muhammad, Nadeem; Subhani, Qamar; Wang, Fenglian; Guo, Dandan; Zhao, Qiming; Wu, Shuchao; Zhu, Yan

    2017-09-15

    This work illustrates the introduction of a simple, rugged and flexible column-switching ion chromatography (IC) technique for an automated on-line QuEChERS extracted samples extracts washing followed by sensitive fluorescence (FLD) determination of five acidic pharmaceutical drugs namely; clofibric acid (CLO), ibuprofen (IBU), aspirin (ASP), naproxen (NAP) and flurobrofen (FLU) in three complex samples (spinach, apple and hospital sewage sludge). An old anion exchange column IonPac ® AS11-HC was utilized as a pre-treatment column for on-line washing of inorganic and organic interferences followed by isocratic separation of five acidic drugs with another anion exchange IonPac ® AS12A analytical column by exploiting the column-switching technique. This novel method exhibited good linearity with correlation coefficients (r 2 ) for all drugs were in the range 0.976-0.996. The limit of detection and quantification of all five acidic drugs were in the range 0.024μg/kg to 8.70μg/kg and 0.082μg/kg to 0.029mg/kg, respectively, and better recoveries in the range 81.17-112.5% with percentage relative standard deviations (RSDs) less than 17.8% were obtained. This on-line sample pre-treatment method showed minimum matrix effect in the range of 0.87-1.25 except for aspirin. This simple rugged and flexible column-switching system required only 28min for maximum elimination of matrices and interferences in three complex samples extracts, isocratic separation of five acidic drugs and for the continuous regeneration of pre-treatment column prior to every subsequent analysis. Finally, this simple automated IC system was appeared so rugged and flexible, which can eliminate and wash out most of interference, impurities and matrices in complex samples, simply by adjusting the NaOH and acetonitrile concentration in washing mobile phase with maximum recoveries of acidic analytes of interest. Copyright © 2017. Published by Elsevier B.V.

  8. Improvement of fuel sampling device for STACY and TRACY

    International Nuclear Information System (INIS)

    Hirose, Hideyuki; Sakuraba, Koichi; Onodera, Seiji

    1998-05-01

    STACY and TRACY, static and transient experiment facilities in NUCEF, use solution fuel. It is important to analyze accurately fuel composition (uranium enrichment, uranium concentration, nitric acid morality, amount of impurities, radioactivity of FP) for their safety operation and improvement of experimental accuracy. Both STACY and TRACY have the sampling devices to sample fuel solution for that purpose. The previous sampling devices of STACY and TRACY had been designed to dilute fuel sample with nitric acid. Its sampling mechanism could pour fuel sample into sampling vessel by a piston drive of nitric acid in the burette. It was, however, sometimes found that sample fuel solution was diluted by mixing with nitric acid in the burette. Therefore, the sampling mechanism was change into a fixed quantity pump drive which didn't use nitric acid. The authors confirmed that the performance of the new sampling device was improved by changing sampling mechanism. It was confirmed through the function test that the uncertainty in uranium concentration measurement using the improved sampling device was 0.14%, and less than the designed value of 0.2% (coefficient of variation). (author)

  9. Classical bile acids in animals, beta-phocaecholic acid in ducks.

    Science.gov (United States)

    Jirsa, M; Klinot, J; Klinotová, E; Ubik, K; Kucera, K

    1989-01-01

    1. Bile samples of different animals were analysed and the percentage content of classical bile acids was determined. 2. Herbivorous birds mostly excreted a large proportion of chenodeoxycholic acid. 3. The anteater (Myrmecophaga tridactyla) excreted deoxycholic acid most probably as a primary bile acid. 4. In the bile of ducks (Anas platyrhynchos) a large amount of (23R)3 alpha, 7 alpha, 23-trihydroxy-5 beta-cholan-24-oic acid (beta-phocaecholic acid) was found.

  10. Fatty Acid Composition of Meat from Ruminants, with Special Emphasis on trans Fatty Acids

    DEFF Research Database (Denmark)

    Leth, Torben; Ovesen, L.; Hansen, K.

    1998-01-01

    The fatty acid composition was determined in 39 samples of beef, 20 samples of veal, and 34 samples of lamb, representative of the supply of ruminant meat in Denmark. Five cuts of beef and veal and three cuts of lamb with increasing fat content were selected, and analysis of the fatty acid methyl...... esters was performed by gas-liquid chromatography (GLC) on a polar 50-m capillary column CP Sil 88 with flame-ionization detection. Lamb had the highest content of saturated fatty acids (52.8 +/- 1.8 g/100 g fatty acids), higher than beef and veal (45.3 +/- 3.1 and 45.4 +/- 0.8 g/100 g fatty acids......, respectively). Cis monounsaturated fatty acids were 49.2 +/- 3.1, 44.9 +/- 1.8, and 37.7 +/- 1.7, and polyunsaturated fatty acids were 3.3 +/- 0.7, 5.8 +/- 2.0, and 5.0 +/- 0.1 g/100 g fatty acids in beef, veal, and lamb, respectively. Beef contained 2.1 +/- 0.8 g trans C-18:1 per 100 g fatty acids, about half...

  11. Kombinasi Boraks dan Asam Borat sebagai Bahan Penghambat Api dan Antirayap Pada Kayu Meranti Merah

    Directory of Open Access Journals (Sweden)

    Mahdi Santoso

    2015-01-01

    improve the quality of wood by impregnating the fire-retardant and anti-termites possessed chemicals. The aim of this research was to investigate the effect of impregnation duration by combination of borax:boric acid ( 1:1 against the fire and termites. This study used red meranti wood (Shorea spp with the dimension of 6 x 15 x 500 cm. The pressure times were 1, 2, and 3 hours as the concentration of borax:boric acid was 7% in 5 replications. Empty cell method was applied as preservation method by 12 kg/cm2 of pressure. Testing the fire resistance referred ASTM E 69-02 B and anti-termite evaluation was conducted by no-choice feeding method. Observed parameters were absorption, actual retention, burn intensity, maximum combustion temperature, glowing time, termite mortality, mass loss, the degree of damage and visual observation. The results showed that the combination of borax: boric acid (1: 1 could improve the quality of red meranti samples against the fire and termite attacks. The most effective impregnation process were 2 hours of pressing time to obtain the 331 kg/ m3 of absorption; actual retention of 28.8 kg/ m3; burnt intensity of 10.9%; maximum combustion temperature of 140ºC; glowing time of 1.03 minutes, termite mortality of 100%; mass loss of 0.002%; and mild degrees of damage category.

  12. Efeito da época de estaquia, fitorreguladores e ácido bórico no enraizamento de estacas de porta-enxertos de videira Effect of pruning time, growth regulators and boric acid on rooting of grape rootstock cuttings

    Directory of Open Access Journals (Sweden)

    S. Leonel

    1993-05-01

    Full Text Available Estudaram-se as interações entre os ácidos indol-butírico, alfa-naftaleno-acético e bórico no desenvolvimento de raízes em estacas de porta-enxertos de videira (Vitis vinifera L.. As estacas tinham aproximadamente 25 cm de comprimento e, necessariamente, 2 gemas, sendo obtidas em três épocas distintas (janeiro, abril e julho e colocadas para enraizar em bandejas de isopor, tendo vermiculita como substrato, e mantidas sob nebulização. O tratamento constou da imersão de 2,5 cm da base das estacas em soluções, por um tempo de imersão de 1 minuto. Os tratamentos utilizados corresponderam a: 1 .000; 2.000 e 5.000 ppm de IBA; 1.500 e 3.000 ppm de NAA; 150 microgramas/ml de H3BO3; IBA 1.000; 2.000 e 5.000 + H3BO3 150 microgramas/ml e H2O. Avaliaram-se a porcentagem de enraizamento, o número médio de raízes formadas por estaca e o comprimento médio das raízes (mm aos 90 dias após a instalação, no mês de julho. O IBA 2.000 ppm propiciou o enraizamento em 88,87% das estacas, contudo não diferiu estatisticamente da testemunha (H2O-61,10%. A melhor época de coleta de estaca para o enraizamento foi o mês de julho (inverno.The effects of indolebutyric, naphtalen acetic and boric acids were studied on rooting of grape rootstock cuttings. The cuttings were 25 cm long with two buds and were taken in three different times (January, April and July. Rooting was carried out in styrofoam trays with vermiculite as substratum and under intermittent mist. Cuttings were imersed up to 2.5 cm from the base in solutions for one minute. The treatments were: 1,000; 2,000 and 5,000 ppm of IBA; 1,500 and 3,000 ppm of NAA; 150 micrograms/ml H3BO3; IBA 1,000; 2,000 and 5,000 ppm plus H3BO(3150 niicrograins/ml and H2O. Rooting percentage, average number of roots per cutting and average length of roots (mm were evaluated 90 days after planting, in July. IBA at 2,000 ppm was the best treatment with 88.8% of rooted cuttings. The best time for rooting was

  13. Termite Resistance of MDF Panels Treated with Various Boron Compounds

    Directory of Open Access Journals (Sweden)

    Sedat Ondaral

    2009-06-01

    Full Text Available In this study, the effects of various boron compounds on the termite resistance of MDF panels were evaluated. Either borax (BX, boric acid (BA, zinc borate (ZB, or sodium perborate tetrahydrate (SPT were added to urea-formaldehyde (UF resin at target contents of 1%, 1.5%, 2% and 2.5% based on dry fiber weight. The panels were then manufactured using 12% urea-formaldehyde resin and 1% NH4Cl. MDF samples from the panels were tested against the subterranean termites, Coptotermes formosanus Shiraki. Laboratory termite resistance tests showed that all samples containing boron compounds had greater resistance against termite attack compared to untreated MDF samples. At the second and third weeks of exposure, nearly 100% termite mortalities were recorded in all boron compound treated samples. The highest termite mortalities were determined in the samples with either BA or BX. Also, it was found that SPT showed notable performance on the termite mortality. As chemical loadings increased, termite mortalities increased, and at the same time the weight losses of the samples decreased.

  14. Boron Removal in Radioactive Liquid Waste by Forward Osmosis Membrane

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Dooseong; Choi, Hei Min; Lee, Kune Woo; Moon Jeikwon [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2014-05-15

    These wastes contain about 0.3-0.8 wt% boric acid and have been concentrated through an evaporation treatment. Boric acid tends to crystallize owing to its solubility, and to plug the evaporator. The volume reduction obtained through evaporation is limited by the amount of boric acid in the waste. As an emerging technology, forward osmosis (FO) has attracted growing interest in wastewater treatment and desalination. FO is a membrane process in which water flows across a semi-permeable membrane from a feed solution of lower osmotic pressure to a draw solution of higher osmotic pressure. However, very few studies on the removal of boron by FO have been performed. The objective of this study is to evaluate the possibility of boron separation in radioactive liquid waste by FO. In this study, the performance of FO was investigated to separate boron in the simulated liquid waste under the factors such as pH, osmotic pressure, ionic strength of the solution, and membrane characteristic. The boron separation in radioactive borate liquid waste was investigated with an FO membrane. When the feed solution containing boron is treated by the FO membrane, the boron permeation depends on the type of membrane, membrane orientation, pH of the feed solution, salt and boron concentration in the feed solution, and osmotic pressure of the draw solution. The boron flux begins to decline from pH 7, and increases with an increase in the osmotic driving force. The boron flux of the CTA-ES and ALFD membrane orientation is higher than those of the CTA-NW and ALFF orientation, respectively. The boron permeation rate is constant regardless of the osmotic pressure and membrane orientation. The boron flux decreases slightly with the salt concentration, but it is not heavily influenced at a low salt concentration.

  15. Boron Removal in Radioactive Liquid Waste by Forward Osmosis Membrane

    International Nuclear Information System (INIS)

    Hwang, Dooseong; Choi, Hei Min; Lee, Kune Woo; Moon Jeikwon

    2014-01-01

    These wastes contain about 0.3-0.8 wt% boric acid and have been concentrated through an evaporation treatment. Boric acid tends to crystallize owing to its solubility, and to plug the evaporator. The volume reduction obtained through evaporation is limited by the amount of boric acid in the waste. As an emerging technology, forward osmosis (FO) has attracted growing interest in wastewater treatment and desalination. FO is a membrane process in which water flows across a semi-permeable membrane from a feed solution of lower osmotic pressure to a draw solution of higher osmotic pressure. However, very few studies on the removal of boron by FO have been performed. The objective of this study is to evaluate the possibility of boron separation in radioactive liquid waste by FO. In this study, the performance of FO was investigated to separate boron in the simulated liquid waste under the factors such as pH, osmotic pressure, ionic strength of the solution, and membrane characteristic. The boron separation in radioactive borate liquid waste was investigated with an FO membrane. When the feed solution containing boron is treated by the FO membrane, the boron permeation depends on the type of membrane, membrane orientation, pH of the feed solution, salt and boron concentration in the feed solution, and osmotic pressure of the draw solution. The boron flux begins to decline from pH 7, and increases with an increase in the osmotic driving force. The boron flux of the CTA-ES and ALFD membrane orientation is higher than those of the CTA-NW and ALFF orientation, respectively. The boron permeation rate is constant regardless of the osmotic pressure and membrane orientation. The boron flux decreases slightly with the salt concentration, but it is not heavily influenced at a low salt concentration

  16. Alternative water chemistry for the primary loop of PWR plants

    Energy Technology Data Exchange (ETDEWEB)

    Henzel, N [Siemens AG Unternehmensbereich KWU, Erlangen (Germany)

    1997-02-01

    Advanced fuel element concepts (longer cycles, higher burnup, increased rod power) call for more reactivity binding capacity and, moreover, might produce higher void fractions, particularly in the hot channel. Thus, on the one hand, more alcalizing agent is needed to maintain a high coolant pH according to the approved ``modified boron-lithium mode of operation`` in the presence of more boric acid (chemical shim); on the other hand, increasing enrichment of coolant constituents due to local boiling (higher void fraction), which must not result in accelerated corrosion of fuel cladding and structural materials, imposes enhanced requirements on both, materials technology and water chemistry. At present, the use of boric acid enriched in B10 (the isotope effective in terms of reactivity control) appears to advantageously compromise in capturing more neutrons with less total boron while maintaining or even slightly reducing lithium concentrations at the same time. There is no feasible alternative for boric acid used as the chemical shim and for hydrogen gas as the reducing agent used to suppress oxygen formation by water radiolysis. Systematic screening as performed in phase 1 of a recent project proved potassium hydroxide to be the only potential candidate to favourably replace lithium 7 hydroxide as an alcalizing agent. Unfortunately, the results of pertinent comparative corrosion tests are not unambiguous, and available operational experience with potassium hydroxide in WWER plants is not readily applicable to western world-type PWR plants. Therefore, a switch-over from lithium to potassium can be envisaged only subsequent to a comprehensive qualification program which is planned to be the objective of phase 2 of the project. This program should also comprise zinc addition tests in order to confirm the alleged positive impact of this element on corrosion rates and activity buildup. (Abstract Truncated)

  17. Experimental study of asymmetric boron dilution at VVER-1000 of Kudankulam NPP and its simulation

    Energy Technology Data Exchange (ETDEWEB)

    Tsyganov, Sergey V.; Kotsarev, Alexander V.; Baykov, Alexander V. [National Research Centre ' ' Kurchatov Institute' ' , Moscow (Russian Federation)

    2017-09-15

    The Kudankulam NPP units contain additional and unique for VVER Quick Boron Injection System (QBIS) for beyond-design-basis accident management without scram. During the physical start-up stage at hot zero power of both Kudankulam units, special tests were performed to assess the efficiency of the system. In the course of test three out of four QBIS tanks had been promptly opened and it led to the asymmetrical injection of boric acid into the core. The scenario of the tests may address to the inhomogeneous boron dilution process that is now an essential part of safety analysis of pressurised water reactors. The simulation of the process, including ex-core ion chambers readings, has been accomplished using ATHLET/BIPR-VVER code. Behaviour of some reactor parameters in the course of the test and some results of the simulation are discussing in the paper. Authors believe the process of the asymmetrical injection of boric acid may be useful for verification and validation of coupled neutronic and thermo-hydraulic codes widely used for safety analysis, including analysis of boron dilution accident.

  18. A review of pH calculation and corrosion product solubilities under PWR primary coolant chemistry conditions

    International Nuclear Information System (INIS)

    Thornton, E.W.; Polley, M.V.

    1986-12-01

    The calculation of high temperature pH in boric acid solutions is discussed and various relationships for the ionisation constant Ksub(w) or ion product Qsub(w) for water are reviewed. It is shown that the boric acid equilibria of Mesmer, Baes and Sweeton remain virtually unaltered when Marshall and Franck's relationship for Ksub(w) is substituted in a re-analysis of Mesmer, Baes and Sweeton's original experimental data. Magnetite solubility data and Westinghouse's studies of iron, nickel and cobalt solubility from mixed ferrites are collated and consideration is given to experimental difficulties which could have contributed to the variability in the data. Thermodynamic model fits have been computerised and used to compare different studies and to determine pH values at which the temperature dependence of solubility is predicted to be zero. Consideration is given to the differing dependences of solubility on dissolved hydrogen concentration in the three model fits. Two models for predicting iron and nickel solubility with respect to non-stoichiometric nickel ferrites are briefly discussed showing that only one of these is likely to be credible. (author)

  19. A simple and efficient method of nickel electrodeposition for the cyclotron production of 64Cu

    International Nuclear Information System (INIS)

    Manrique-Arias, Juan C.; Avila-Rodriguez, Miguel A.

    2014-01-01

    Nickel targets for the cyclotron production of 64 Cu were prepared by electrodeposition on a gold backing from nickel chloride solutions using boric acid as buffer. Parameters studied were nickel chloride and boric acid concentration, temperature and current density. All plating conditions studied were successful obtaining efficiencies of approximately 90% in 2–3 h, reaching almost quantitative plating (>97%) in 10–20 h depending on the current density. All plated targets withstood proton irradiations up to 40 µA for 2 h. Recovered nickel was successfully recycled and reused with an overall efficiency >95%. - Highlights: • Simple and efficient method of Ni electrodeposition from NiCl 2 solutions. • Represents an improvement over current methods for the preparation of Ni targets. • All plated targets underwent irradiation and withstood currents up to 40 µA for 2 h. • Nickel target material was recycled and reused with an overall efficiency >95%. • Specific activity of 64 Cu was similar than that obtained with older methods of Ni plating

  20. Comparison of EPR response of alanine and Gd₂O₃-alanine dosimeters exposed to TRIGA Mainz reactor.

    Science.gov (United States)

    Marrale, M; Schmitz, T; Gallo, S; Hampel, G; Longo, A; Panzeca, S; Tranchina, L

    2015-12-01

    In this work we report some preliminary results regarding the analysis of electron paramagnetic resonance (EPR) response of alanine pellets and alanine pellets added with gadolinium used for dosimetry at the TRIGA research reactor in Mainz, Germany. Two set-ups were evaluated: irradiation inside PMMA phantom and irradiation inside boric acid phantom. We observed that the presence of Gd2O3 inside alanine pellets increases the EPR signal by a factor of 3.45 and 1.24 in case of PMMA and boric acid phantoms, respectively. We can conclude that in the case of neutron beam with a predominant thermal neutron component the addition of gadolinium oxide can significantly improve neutron sensitivity of alanine pellets. Monte Carlo (MC) simulations of both response of alanine and Gd-added alanine pellets with FLUKA code were performed and a good agreement was achieved for pure alanine dosimeters. For Gd2O3-alanine deviations between MC simulations and experimental data were observed and discussed. Copyright © 2015 Elsevier Ltd. All rights reserved.

  1. Improvement on control of waste disposal system at Genkai Nuclear Power Station No.1 and No.2 unit

    International Nuclear Information System (INIS)

    Morooka, Masatoshi; Tsutsumi, Akria

    1989-01-01

    At Genkai Nuclear Power Station, the operational and control systems of the boric acid evaporator, waste liquid evaporator and gaseous waste disposal system were converted from general purpose analong systems to computer instrumentation and control systems in order to improve their operability and controllability. The equipments were operated by batch processing system, so plant operators were required to operate them manually. By introducing the computer instrumentation and control systems, the automatic operation of the equipments has become possible. Furthermore, it has become possible to monitor the relevant parameters intensively with a CRT in the operating room, and it contributes to the improvement of reliability and labor saving. The operation of No.1 plant was begun in October, 1975, and No.2 plant in March, 1981. Both are the PWR plants of 625 MVA capacity. The outline of the power station facilities, the background of the reconstruction, the problems and the plan of reconstruction for the boric acid recovery facility, waste liquid evaporator and gas compressor, the peculiarity of the reconstruction works, and the effect of introducing the new systems are reported. (Kako, I.)

  2. [Determination of fatty acid esters of chloropropanediols in diet samples by gas chromatography-mass spectrometry coupled with solid-supported liquid-liquid extraction].

    Science.gov (United States)

    Gao, Jie; Liu, Qing; Han, Feng; Miao, Hong; Zhao, Yunfeng; Wu, Yongning

    2014-05-01

    To establish a method for the determination of fatty acid esters of 3-monochloropropane-1, 2-diol (3-MCPD) and 2-monochloropropane-1, 3-diol (2-MCPD) in diet samples by gas chromatography-mass spectrometry (GC-MS) with solid-supported liquid-liquid extraction (SLE). Diet samples were ultrasonically extracted by hexane, followed by ester cleavage reaction with sodium methylate in methanol, and then purified by solid-supported liquid-liquid extraction. (SLE) using diatomaceous earth as the sorbent. After derivatization with heptafluorobutyrylimidazole, the analytes were detected by GC-MS and quantified by the deuterated internal standards. The limits of detection (LODs) of 3-MCPD esters and 2-MCPD esters in different diet samples were 0.002 - 0.005 mg/kg and 0.002 - 0.006 mg/kg. The average recoveries of 3-MCPD esters and 2-MCPD esters at the spiking levels of 0.05 and 0.1 mg/kg in the diet samples were in the range of 65.9% - 104.2% and 75.4% - 118.0%, respectively, with the relative standard deviations in the range of 2.2% - 14.2% and 0.8% - .13.9%. The method is simple, accurate and rugged for the determination of fatty acid esters of 3-MCPD and 2-MCPD in diet samples.

  3. Syringe needle-based sampling coupled with liquid-phase extraction for determination of the three-dimensional distribution of l-ascorbic acid in apples.

    Science.gov (United States)

    Tang, Sheng; Lee, Hian Kee

    2016-05-15

    A novel syringe needle-based sampling approach coupled with liquid-phase extraction (NBS-LPE) was developed and applied to the extraction of l-ascorbic acid (AsA) in apple. In NBS-LPE, only a small amount of apple flesh (ca. 10mg) was sampled directly using a syringe needle and placed in a glass insert for liquid extraction of AsA by 80 μL oxalic acid-acetic acid. The extract was then directly analyzed by liquid chromatography. This new procedure is simple, convenient, almost organic solvent free, and causes far less damage to the fruit. To demonstrate the applicability of NBS-LPE, AsA levels at different sampling points in a single apple were determined to reveal the spatial distribution of the analyte in a three-dimensional model. The results also showed that this method had good sensitivity (limit of detection of 0.0097 mg/100g; limit of quantification of 0.0323 mg/100g), acceptable reproducibility (relative standard deviation of 5.01% (n=6)), a wide linear range of between 0.05 and 50mg/100g, and good linearity (r(2)=0.9921). This interesting extraction technique and modeling approach can be used to measure and monitor a wide range of compounds in various parts of different soft-matrix fruits and vegetables, including single specimens. Copyright © 2015 Elsevier Ltd. All rights reserved.

  4. Studies on the interference of hydrofluoric acid and phosphoric acid in the determination of uranium using Ti(III) reduction method-biamperometry end point

    International Nuclear Information System (INIS)

    Shiny, T.S.; Rajalakshmi, A.; Phal, D.G.; Charyulu, M.M.; Ramakumar, K.L.

    2007-01-01

    Accurate and precise determination of uranium in nuclear materials is necessary for chemical quality control as well as for nuclear material accounting purposes. Different types of uranium samples are received for the measurements. Depending upon the nature of the sample dissolution procedure is selected. Mixed oxide samples of uranium and plutonium, for example, are dissolved in nitric acid containing hydrofluoric acid under IR lamp. The fluoride ions are removed by repeated evaporation of the solution. However, some fluoride ions are left in the solutions depending on the conditions of evaporation. Uranium samples and alloy samples are dissolved in dilute hydrochloric acid. The rate of dissolution depends on concentration of acid. Sometimes a mixture of hydrochloric acid and hydrofluoric acid is used for the dissolution metal alloy samples, which may contain silica. Another method of dissolution of these samples is using a mixture of phosphoric acid and 1% hydrofluoric acid. It is necessary to study the interference of hydrofluoric acid and phosphoric acid on the determination of uranium

  5. Determination of low concentrations of thorium in granites using X-ray fluorescence technique

    International Nuclear Information System (INIS)

    Shigematsu, H.M.; Sato, I.M.; Iyer, S.S.

    1981-03-01

    An analytical method for the accurate determination of low concentrations of thorium in rocks using X-ray fluorescence technique, was developed. A tungsten tube was utilized for the production of X-rays. The samples were prepared in the form of double layer pressed pellets using boric acid as a binding agent. The concentration of thorium was determined by measuring the intensity of the characteristic first order Th L α line. The calibration was carried out with USGS rock standards AGV-1, GSP-1 and G-2. Seven granite rocks samples from Granite Mountains of Wyoming, USA, supplied by Dr. Stuckless. Also were analysed. The results obtained were compared with values obtained in others laboratories using different analytical methods. The analyses show that the thorium is concentrated in accessory minerals and presented a non-uniform distribution, making sampling an important factor in the analysis of thorium. A discussion of the precision and accuracy of the method is presented. (Author) [pt

  6. Oxalic acid as a liquid dosimeter for absorbed dose measurement in large-scale of sample solution

    International Nuclear Information System (INIS)

    Biramontri, S.; Dechburam, S.; Vitittheeranon, A.; Wanitsuksombut, W.; Thongmitr, W.

    1999-01-01

    This study shows the feasibility for, applying 2.5 mM aqueous oxalic acid solution using spectrophotometric analysis method for absorbed dose measurement from 1 to 10 kGy in a large-scale of sample solution. The optimum wavelength of 220 nm was selected. The stability of the response of the dosimeter over 25 days was better than 1 % for unirradiated and ± 2% for irradiated solution. The reproducibility in the same batch was within 1%. The variation of the dosimeter response between batches was also studied. (author)

  7. Multiplexed microfluidic approach for nucleic acid enrichment

    Science.gov (United States)

    VanderNoot, Victoria A.; Langevin, Stanley Alan; Bent, Zachary; Renzi, Ronald F.; Ferko, Scott M.; Van De Vreugde, James L.; Lane, Todd; Patel, Kamlesh; Branda, Steven

    2016-04-26

    A system for enhancing a nucleic acid sample may include a one pump, a denaturing chamber; a microfluidic hydroxyapatite chromatography device configured for performing hydroxyapatite chromatography on the nucleic acid sample, a sample collector, and tubing connecting the pump with the denaturing chamber, the hydroxyapatite chromatography device and the sample collector such that the pump may be used to move the nucleic acid sample from the denaturing chamber to the hydroxyapatite chromatography device and then to the sample collector.

  8. Fire-retardant-treated strandboard : properties and fire performance

    Science.gov (United States)

    Jerrold Winandy; Qingwen Wang; Robert H. White

    2008-01-01

    This study evaluated a series of single-layer, randomly oriented strandboard panels made with one resin type, a single resin loading level, and four fire-retardant-treatment levels. The fire retardant (FR) evaluated was a pH-buffered combination of boric acid and organic phosphate. Siberian larch strands were separated into five batches. One batch of strands served as...

  9. PWR auxiliary systems, safety and emergency systems, accident analysis, operation

    International Nuclear Information System (INIS)

    Meyer, P.J.

    1976-01-01

    The author presents a description of PWR auxiliary systems like volume control, boric acid control, coolant purification, -degassing, -storage and -treatment system and waste processing systems. Residual heat removal systems, emergency systems and containment designs are discussed. As an accident analysis the author gives a survey over malfunctions and disturbances in the field of reactor operations. (TK) [de

  10. Effect of Boron and Phosphate compounds on Thermal and Fire Properties of wood/HDPE composites

    Science.gov (United States)

    Turgay Akbulut; Nadir Ayrilmis; Turker Dundar; Ali Durmus; Robert H. White; Murat Teker

    2011-01-01

    Melting and non-isothermal crystallization behaviors, oxidative induction time, and fire performance of the injection-molded wood flour-high density polyethylene (HDPE) composites (WPCs) incorporated with different levels (4, 8, or 12 wt %) of boron compounds [borax/boric acid (BX/BA) (0.5:0.5 wt %), zinc borate (ZB)] and phosphorus compounds [mono- and di-ammonium...

  11. Dismountable wall for radiation shielding and screen realized from this wall

    International Nuclear Information System (INIS)

    Blomart, P.

    1988-01-01

    The wall for protection against neutrons and gamma radiations is made of bricks with a shoulder on the upper and side faces and the complementary shape on the lower face to provide a barrier to radiations. Bricks are made of a heavy material for gamma absorption and of epoxy resin, boric acid and hydrated alumina [fr

  12. 77 FR 43382 - Millstone Power Station, Unit 2; Exemption

    Science.gov (United States)

    2012-07-24

    ... Transition from Main Steam Safety Valves. Check Local Condensate Storage OMA 20 Tank Level Indication at LIS-5489. Open Breaker to Fail Valve 2-CH- OMA 6 517 Closed. Check Local Level Indication at LI- OMA 18 206A. Check Local Boric Acid Storage OMA 19 Tank Level Indication at LI-208A. Open Valve 2-CH-429 to...

  13. Synthesis of nanocrystalline TiO 2 thin films by liquid phase ...

    Indian Academy of Sciences (India)

    A transparent, high purity titanium dioxide thin film composed of densely packed nanometer sized grains has been successfully deposited on a glass substrate at 30°C from an aqueous solution of TiO2–HF with the addition of boric acid as a scavenger by liquid phase deposition technique. From X-ray diffraction ...

  14. ELECTROCHEMICAL DETERMINATION OF ETHANOL, 2 ...

    African Journals Online (AJOL)

    2014-12-31

    Dec 31, 2014 ... ABSTRACT. In this work, we present the modification of a glassy carbon electrode with nickel oxide film which is performed in two successive steps. In the first one, the electrochemical deposition of metallic nickel on the glassy carbon electrode (GCE) is achieved in 0.1M boric acid; in the second step, the ...

  15. Use of X-ray fluorescence analysis for the determination of hafnium in zircalloys

    International Nuclear Information System (INIS)

    Sato, I.M.; Salvador, V.L.R.; Lordello, A.R.

    1985-01-01

    The determination of hafnium at trace levels (ppm) in the presence of zirconium by X-ray fluorescence technique is presented. The samples were prepared in the form of double-layer pellets, with boric acid as the binding material. The most sensitive first order line of hafnium HfLα (0.157 nm), which is used analyticaly, has approximately 67% overlapping with second order line of zirconium ZrKα 1 , (0.079 nm). As the excitation potencial of zirconium is larger than hafnium, the best condition was selected, so that the interference of zirconium intensity would not be significant in hafnium analytical line. The method allowed the determination of hafnium above 5.0 ppm (LLd = 1.5 ppm) with an accuracy of less than 10%. (Author) [pt

  16. Determination of rubidium and strontium in geological materials by X-Ray fluorescence spectrometry

    International Nuclear Information System (INIS)

    Roca, M.

    1979-01-01

    In order to determine whole-rock ages by the Rb/Sr procedure, an X-ray fluorescence spectrometry method for the determination of both elements has been developed. The samples are pressed into boric acid backed and ringed pellets with this material as a binding agent. Matrix corrections are made following the determination od the mass absorption coefficients, based on the intensity of the Compton-scattered peak of MoKα. or MoKβ 1 .3. The U. S. Geological Survey granodiorite GSP-1 is used as a reference standard. Spectral-line interferences have been carefully studied and the empirical correction factors determined. A BASIC language program for calculating the Rb and Sr concentrations and the Rb/Sr ratios has been written. (Author) 7 refs

  17. Determination of rubidium and strontium in geological materials by X-Ray fluorescence spectrometry; Determinacion de rubidio y estroncio en materiales geologicos mediante espectrometria de fluorescencia de rayos X

    Energy Technology Data Exchange (ETDEWEB)

    Roca, M.

    1979-07-01

    In order to determine whole-rock ages by the Rb/Sr procedure, an X-ray fluorescence spectrometry method for the determination of both elements has been developed. The samples are pressed into boric acid backed and ringed pellets with this material as a binding agent. Matrix corrections are made following the determination od the mass absorption coefficients, based on the intensity of the Compton-scattered peak of MoK{alpha}. or MoK{beta}{sub 1}.3. The U. S. Geological Survey granodiorite GSP-1 is used as a reference standard. Spectral-line interferences have been carefully studied and the empirical correction factors determined. A BASIC language program for calculating the Rb and Sr concentrations and the Rb/Sr ratios has been written. (Author) 7 refs.

  18. Determination of trace metals in nuclear-grade uranium dioxide by X-ray fluorescence spectrometry

    International Nuclear Information System (INIS)

    Salvador, V.L.R.; Imakuma, K.

    1988-04-01

    A method is described for the simultaneous determination of low concentrations of Ca, Cr, Cu, Fe, Mn and Ni in nuclear-grade uranium dioxide by X-ray fluorescence spectrometry, without the use of chemical treatment. The lower limits of detection range from 2 μg g -1 for nickel and manganese to 5 μg g -1 for copper. Samples are prepared in the form of double-layer pellets with boric acid as a binding agent. Standards are prepared in a U 3 O 8 matrix, which is more chemically stable than UO 2 and has similar matrix behaviour. The correlation coefficients for calibration curves are better than 0.999. Erros range from 2.4 % for chromium to 6.8 % for nickel. (author) [pt

  19. [Trace analysis of aristolochic acid A].

    Science.gov (United States)

    Liu, Yalin; Gao, Huimin; Wang, Zhimin; Zhang, Qiwei

    2010-12-01

    A HPLC method for limit detection of aristolochic acid A in the Chinese herbs containing aristolochic acid or suspected-containing aristolochic acid and their preparations was established. The samples were analyzed on an Alltima C18 column eluted with methanol-water-acetic acid (68:32:1.5) as the mobile phase. Flow rate was at 1.0 mL x min(-1) and the detection wavelength was at 390 nm. The calibration curve was linear over the range from 0.016 to 0.51 g (r = 0.9993) and LOD was 4 ng. The average recovery was 101.2% with RSD of 2.01%. The procedures of sample preparation were systematically investigated. The contents of aristolochic acid A in Radix et Rhizoma Asari bought from market or drugstore were fluctuated from 3.1 to 26.6 microg x g(-1) and 3 of 11 samples accorded with the quality requirement of current Chinese Pharmacopoeia. Among 15 batches samples of Chinese medicaments, only one sample was found to contain aristolochic acid A. The present investigation shows that the method is sensitive and repeatable and it could be used for the limit detection of aristolochic acid A in the Chinese herbal medicines containing trace amount of aristolochic acid A or suspected-containing aristolochic acid A and their preparations.

  20. Characterization of acid tars

    Energy Technology Data Exchange (ETDEWEB)

    Leonard, Sunday A., E-mail: sunday.leonard@ucl.ac.uk [Department of Civil Environmental and Geomatic Engineering, University College London, Chadwick Building, Gower Street, London, WC1E 6BT (United Kingdom); Stegemann, Julia A. [Department of Civil Environmental and Geomatic Engineering, University College London, Chadwick Building, Gower Street, London, WC1E 6BT (United Kingdom); Roy, Amitava [J. Bennett Johnston, Sr., Centre for Advance Microstructures and Devices (CAMD), 6980 Jefferson Highway, Louisiana State University, Baton Rouge, LA, 70806 (United States)

    2010-03-15

    Acid tars from the processing of petroleum and petrochemicals using sulfuric acid were characterized by gas chromatography/mass spectrometry (GC/MS), inductively coupled plasma/optical emission spectrometry (ICP/OES), differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectrometry, and scanning electron microscopy/energy dispersive X-ray (SEM/EDX) micro-analysis. Leaching of contaminants from the acid tars in 48 h batch tests with distilled water at a liquid-to-solid ratio 10:1 was also studied. GC/MS results show that the samples contained aliphatic hydrocarbons, cyclic hydrocarbons, up to 12 of the 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs), and numerous other organic groups, including organic acids (sulfonic acids, carboxylic acids and aromatic acids), phenyl, nitrile, amide, furans, thiophenes, pyrroles, and phthalates, many of which are toxic. Metals analysis shows that Pb was present in significant concentration. DSC results show different transition peaks in the studied samples, demonstrating their complexity and variability. FTIR analysis further confirmed the presence of the organic groups detected by GC/MS. The SEM/EDX micro-analysis results provided insight on the surface characteristics of the samples and show that contaminants distribution was heterogeneous. The results provide useful data on the composition, complexity, and variability of acid tars; information which hitherto have been scarce in public domain.