SU387275A1 - METHOD OF ANALYZING EXTRACTORS BASED ON NEUTRAL AIR MIXTURE - Google Patents

METHOD OF ANALYZING EXTRACTORS BASED ON NEUTRAL AIR MIXTURE

Info

Publication number
SU387275A1
SU387275A1 SU1450686A SU1450686A SU387275A1 SU 387275 A1 SU387275 A1 SU 387275A1 SU 1450686 A SU1450686 A SU 1450686A SU 1450686 A SU1450686 A SU 1450686A SU 387275 A1 SU387275 A1 SU 387275A1
Authority
SU
USSR - Soviet Union
Prior art keywords
analyzing
air mixture
extractant
tbp
content
Prior art date
Application number
SU1450686A
Other languages
Russian (ru)
Inventor
М. Бобрик В.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to SU1450686A priority Critical patent/SU387275A1/en
Application granted granted Critical
Publication of SU387275A1 publication Critical patent/SU387275A1/en

Links

Landscapes

  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

Description

1one

Изобретение относитс  к аналитической химии , в частности к контролю процессов экстракции редких   рассе нных элементов.This invention relates to analytical chemistry, in particular, to the control of the extraction processes of rare scattered elements.

В насто щее врем  дл  анализа экстрагентов на основе ТБФ с добавкой алкилфосфорных кислот (например Д2ЭГФК) в инертном растворителе (обычно 1керосине) примен ют спектрофотометрические методы, которые требуют применени  сложных в эксплуатации приборов и высокой квалификации исполнителей .At present, spectrophotometric methods are used to analyze TBP-based extractants with the addition of alkyl phosphoric acids (e.g. D2EHPA) in an inert solvent (usually 1kerosene), which require the use of sophisticated instruments and highly skilled performers.

Цель изобретени  - раз,рабо11ка ускоренного способа анализа экстрагентов, представл ющих собой смесь нейтральных фосфорных и алкилфосфорных кислот, нригодного дл  оперативного контрол  производства.The purpose of the invention is the development of an accelerated method for the analysis of extractants, which are a mixture of neutral phosphoric and alkylphosphoric acids, which is not useful for the operational control of production.

По предлагаемому способу производ т две серии измерений диэлектрической проницаемости (ДП) экстрагента на основе нейтральных эфирОВ фосфорной кислоты (например ТБФ) и алкилфосфорных кислот (например Д2ЭГФК): 1) свободного зкстрагента; 2) отработанного раствором азотной кислоты концентрацией 0,75-1,5 .According to the proposed method, two series of measurements of the dielectric constant (DP) of the extractant based on neutral ethers of phosphoric acid (for example TBP) and alkyl phosphoric acids (for example D2EHPA) are carried out: 1) free extractor; 2) spent with a solution of nitric acid with a concentration of 0.75-1.5.

ДП нейтральный эфиров фосфорной кислоты и алкилфосфорных кислот наход тс  в пределах 7-9, тогда: как ДП растворител  (керосина) значительно меньше - 2. Таким образом, первое измерение ДП дает содержание суммы экстрагирующих веществ в керосине .DP neutral esters of phosphoric acid and alkylphosphoric acids are in the range of 7-9, then: as the DP of the solvent (kerosene) is significantly less - 2. Thus, the first measurement of the DP gives the content of the sum of extracting substances in kerosene.

При Об ра;бот1ке экстр агента раствором азотной кислоты определенной умеренной концентрации ТБФ 1прев1ращае11с  в азотнокислые комплексы, ДП которых значительно выше, чем у исходного экстрагеита. Алкилфосфорные кислоты не поглощают азотную кислоту из ее растворов умеренной концентрации. ТакимAt Obs; an extra agent with a solution of nitric acid of a certain moderate concentration of TBP 1 transforms into nitric acid complexes, the DP of which is significantly higher than that of the original extractgeite. Alkyl phosphoric acids do not absorb nitric acid from its solutions of moderate concentration. So

образом, второе из)мерение ДП дает содержание ТБФ в экстрагенте, пропорциональное приращению ДП зкстрагента после обработки азотной кислотой. Содержание алкилфосфорной кислоты находитс  из разности.Thus, the second of the measurements of DP gives the TBP content in the extractant, which is proportional to the increment of the PD extractant after treatment with nitric acid. The content of alkylphosphoric acid is from the difference.

Предлагаемый способ позвол ет проводить анализ экстрагентов с применением простого в эксплуатации прибора-измерител  диэлектрической проницаемости (электрической емкости ).The proposed method allows the analysis of extractants using an easy-to-use dielectric permittivity meter (electrical capacitance).

Пример. Дл  определени  содержани  Д2ЭГФК и ТБФ в экстрагенте на основе керосина готов т серию стандартных смесей индивидуальных э кстрагентов с керосином иExample. To determine the content of D2EHPA and TBP in a kerosene-based extractant, a series of standard mixtures of individual extras with kerosene and

стро т два графика зависимостей ДП экстра гейта от содержани . Серию стандартов на основе ТБФ обрабатывают 1 М раствором азотной кислоты при отношении фаз органическа  :1водна  1 : I и на основе измеренийTwo graphs of DP extra dependencies on the content are plotted. A series of standards based on TBP is treated with a 1 M solution of nitric acid with an organic: 1 water ratio of 1: I and based on measurements

ДП стро т трет1ИЙ график зависимости приращени  ДП экстрагента от содержани  в нем ТБФ. (The DP builds a tertiary plot of the increment of the DP extractant on the TBP content. (

Пробу экстрагента неизвестного состава после реакции поглощенных «омпонентов и промывюи водой подвергают замеру ДП, затем обрабатывают 1 М раствором азотной кислоты при отношении органическа  : водна  1:1 И«HOSib измер ют ДП.ПрИ:ра|щение ДП по третьему (Графику дает содержание ТБФ. По найденному содержанию ТБФ наход т соответствующую ему величину ДП по калибровочному графику. Эту величину вычитают из -величины ДП экстрагента ino первому замеру и 1ПО калибровочному графику дл  Д2ЭГФК наход т содержание .последней.A sample of an extractant of unknown composition after the reaction of absorbed components and washing with water is subjected to measurement of DP, then treated with 1 M solution of nitric acid at an organic: aqueous ratio 1: 1 AND "HOSib" measure DP. PIP: DP increase by the third (Graph TBP. According to the found TBP content, the corresponding DP value is found according to the calibration schedule. This value is subtracted from the DP extractant ino value to the first measurement and 1PO calibration chart for D2EHPK to find the content last.

В широком интервале концентраций нейтральных эфиров фосфорной кислоты и алкилфоофорных кислот сохран етс  аддиктивность ДП экстратента и мала  зависимость приращени  ДП ТБФ после обра1ботки азотной кислотой от содержани  алкилфосфорной .кислоты .In a wide range of concentrations of neutral esters of phosphoric acid and alkyl phosphoric acids, the additivity of DP extractant remains and the increment of DP TBP increment after treatment with nitric acid on the content of alkyl phosphoric acid remains low.

Предмет изобретени Subject invention

Способ анализа.Э1Кстраге:нто(в на основе смеси нейтральных эфиров фосфорной кислоты и алкйлфосфорных кислот в инертных раз бавител х по диэлектрической проницаемости,Method of analysis. E1Kstrague: nto (in based on a mixture of neutral phosphoric acid esters and alkyl phosphoric acids in inert dilutions on the dielectric constant,

отличающийс  тем, что, с целью ускорени  анализа и дифференцированного определени  исследуемых веществ, экстрагент -перед измерением обрабатывают раствором азотной -кислоты концентрацией 0,75-1,5 моль/л и измер ют приращение величины его диэлектр ческой пр01НИ|Ца.емо1Сти, лр.опорциоеально.е содержанию нейтрального эфира, -которое сравнивают с диэлектрической проницаемостью необработанного экстрагента.characterized in that, in order to speed up the analysis and differentiated determination of the test substances, the extractant is treated with a solution of 0.75-1.5 mol / l before measuring and the increment of its dielectric value is measured .portsiooealno.e content of neutral ether, which is compared with the dielectric constant of the raw extractant.

SU1450686A 1970-06-19 1970-06-19 METHOD OF ANALYZING EXTRACTORS BASED ON NEUTRAL AIR MIXTURE SU387275A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1450686A SU387275A1 (en) 1970-06-19 1970-06-19 METHOD OF ANALYZING EXTRACTORS BASED ON NEUTRAL AIR MIXTURE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1450686A SU387275A1 (en) 1970-06-19 1970-06-19 METHOD OF ANALYZING EXTRACTORS BASED ON NEUTRAL AIR MIXTURE

Publications (1)

Publication Number Publication Date
SU387275A1 true SU387275A1 (en) 1973-06-21

Family

ID=20454236

Family Applications (1)

Application Number Title Priority Date Filing Date
SU1450686A SU387275A1 (en) 1970-06-19 1970-06-19 METHOD OF ANALYZING EXTRACTORS BASED ON NEUTRAL AIR MIXTURE

Country Status (1)

Country Link
SU (1) SU387275A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012047402A1 (en) * 2010-10-06 2012-04-12 The Boeing Company Extraction method and system for monitoring for the presence of phosphate esters in jet fuel

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012047402A1 (en) * 2010-10-06 2012-04-12 The Boeing Company Extraction method and system for monitoring for the presence of phosphate esters in jet fuel
US8426212B2 (en) 2010-10-06 2013-04-23 The Boeing Company Method and system for monitoring for the presence of phosphate esters in jet fuel
CN105388269A (en) * 2010-10-06 2016-03-09 波音公司 Method and system for monitoring for the presence of phosphate esters in jet fuel

Similar Documents

Publication Publication Date Title
KR101470363B1 (en) Method for elemental analysis by isotope dilution inductively-coupled plasma mass spectrometry coupled with combustion sample preparation
CN103900990B (en) The method of plutonium and nitric acid content in Rapid Simultaneous Determination organic facies
CN105891374A (en) Detection method for measuring eight preservatives in reconstituted tobaccos simultaneously
Sinclair An ‘AutoAnalyzer’method for determination of extractable sulphate in soil
SU387275A1 (en) METHOD OF ANALYZING EXTRACTORS BASED ON NEUTRAL AIR MIXTURE
Klinghoffer et al. Flow-injection analysis of traces of lead and cadmium by solvent extraction with dithizone
CN105372371A (en) Ion chromatography method for simultaneous determination of oxalic ion, succinate ion, sulfate ion and phosphate ion in reconstituted tobacco and application thereof
CN105334283B (en) Simultaneous Determination reconstituted tobacco oxalate, amber acid radical, the sample-pretreating method of sulfate radical and phosphate radical
JPH07146284A (en) Safe analytical method for measurement of concentration of decomposition product in solvent used for solvent extraction
CN109239004B (en) Method for analyzing components of fatty acid-containing and fatty acid derivative compound
JP5622543B2 (en) Method for quantitative analysis of higher fatty acids contained in inorganic powders
CN112461945B (en) Method for simultaneously and rapidly analyzing dibutyl phosphate, monobutyl phosphate, n-butyric acid, NO 3-and NO2-
Chandramouleeswaran et al. Insight of solvent extraction process: Reassessment of trace level determinations
JP2023012339A (en) Method for analyzing concentrations of fluorine and compound thereof
Whitman et al. Extraction of Magnesium with 8-Quinolinol
McAlister et al. A method for the separation of beryllium from spectral interfering elements in inductively coupled plasma-atomic emission spectroscopic analysis
CN103398968A (en) Method for detecting 2-methylisoborneol in water
CN115326984B (en) Method for measuring content of baicalin metal complex by HPLC (high Performance liquid chromatography)
Hughes et al. The estimation of phosphine in air
RU2779479C1 (en) Method for luminescent determination of yttrium (iii)
CN115343410B (en) Method for quantitatively measuring acid concentration in perchloric acid-containing mixed acid etching solution
Englmaier Nitrate analysis by gas-liquid chromatography using the nitration of 2, 4-dimethylphenol in sulphuric acid
SU142809A1 (en) Method for analytical determination of extractants
CN111855644A (en) Method for enriching and quantifying rare earth elements in solubility product driven electrolyte
JP2023508654A (en) Method for determining acidity of acidic aqueous solutions