SU95772A1 - Method for determination of small amounts of divalent manganese - Google Patents
Method for determination of small amounts of divalent manganeseInfo
- Publication number
- SU95772A1 SU95772A1 SU44.3831A SU443831A SU95772A1 SU 95772 A1 SU95772 A1 SU 95772A1 SU 443831 A SU443831 A SU 443831A SU 95772 A1 SU95772 A1 SU 95772A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- solution
- small amounts
- determination
- divalent manganese
- manganese
- Prior art date
Links
- 239000011572 manganese Substances 0.000 title description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 title description 6
- 229910052748 manganese Inorganic materials 0.000 title description 6
- 238000000034 method Methods 0.000 title description 5
- 239000000243 solution Substances 0.000 description 20
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000012086 standard solution Substances 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 244000125300 Argania sideroxylon Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 101150111724 MEP1 gene Proteins 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical class [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 239000012088 reference solution Substances 0.000 description 1
- JZWFDVDETGFGFC-UHFFFAOYSA-N salacetamide Chemical group CC(=O)NC(=O)C1=CC=CC=C1O JZWFDVDETGFGFC-UHFFFAOYSA-N 0.000 description 1
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
Landscapes
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Description
Известны способы определени двухвалентного марганца по :редством окислительно-васстановительной реакции, напэимер с фо)мальдOXCи oм . Однако при этом п 1едварителько требуетс производить отделение железа.Methods are known for the determination of divalent manganese by: the redox reaction, the naphimer with phyldohaloxo and o. However, at the same time, it is required to make iron separation once a quarter.
Предлагаемый спос.об сокращает врем анализа, так как позвол ет производить определение малых количеств двухва.чентного лгарганца в присутствии небольших количеств железа и отличаетс от известных тем, что определение цроизвод т посредством реакции с са 1ицилальорто-аминофенолом .The proposed method shortens the analysis time, as it allows the determination of small amounts of two-bv argans in the presence of small amounts of iron and differs from those known in that the definition is produced by reaction with calcium cyanalorto-aminophenol.
Способ заключаетс в следую1цем .The method is as follows.
В испытуемый раствор с рН 9,7-11,6, содержащий хлористый аммоний прибав п ют 0,05%-ного спиртового раствора азометина, получаемого конденсацией салицилового альдегида с орто-аминофенолом , и сравнивают окраску испытуемого раствора после добавлени формал:ина (дл стабилизации окраски) с окраской эталонных растворов. Открываемый минимум составл ет 0,25 7 { Т 0,001 мг) марганца в 5 мл раствора, что отвечает пpeдe. разоав,1ению 1:2. 10чAmmonium chloride containing 0.05% alcoholic solution of azomethine obtained by condensation of salicylic aldehyde with ortho-aminophenol is added to the test solution with pH 9.7-11.6, and the color of the test solution is compared after adding the formal: other (for color stabilization) with the color of standard solutions. The opening minimum is 0.25 7 {T 0.001 mg) of manganese in 5 ml of solution, which corresponds to a precursor. Having said 1: 2. 10h
П р 11 м е р -1. Опреде.:1ение катиона Мп в прнсутствии других катионов .PR 11 mep -1. Definition: 1: cation of Mp in the presence of other cations.
В pacTBOj), содержании от 0,25 до БуМп, прибавл ют 1 мл 1()-ного раствора .х,ло)истого аммони и добавкой воды o6iieM довод т до 5 M.I. К раствору прибавл ют 0,1 -ил 0,05| спиртово1о jiacTBOpa салицила .1ь-орто-ам1 нофенола (азометина ) п iiocie перемешивани 0,2 м.г 2()о-ного раствора едкого нат1)а. По в.чение окраски, в результате взаимодействи катиона Мп с азометином, происходит при j)H среды в ин1ерва..1е от 9,7 до 11,6 с одинаково интенсивностью; прл рН 9-9,2 возникающа окраска несколько бледней; при рН, paBHoii 6-7, уже не наблюдаетс изменени ЖС.1ТОЙ окраски реагента. Окраска, возникаюн,а при благопри тной величине рН от наличи марганца, разви ваетс со временем (при комнатной температуре) и через 10 мин. достигает своей наибольшей , пропорциональной количеству марганца, интенсивности, котора в данных услови х можетIn pacTBOj), the content is from 0.25 to BuMn, 1 ml of a 1 () solution of .x, low ammonium hydroxide and o6iieM water is added to 5 M.I. 0.1 -1.0.05 is added to the solution | alcoholic jiacTBOpa salicyl .1-ortho-am1 nophenol (azomethine) p iiocie mixing 0.2 m g 2 () of a caustic solution of sodium (1) a. According to the color of the coloration, as a result of the interaction of the Mp cation with azomethine, occurs at j) H of the medium in a1.1.1 from 9.7 to 11.6 with the same intensity; In the pH range of 9-9.2, the resulting color is somewhat paler; at pH, paBHoii 6–7, there is no longer a change in LC.1 TO color of the reagent. The color arises, and with a favorable pH value from the presence of manganese, it develops with time (at room temperature) and after 10 minutes. reaches its highest, proportional to the amount of manganese, intensity, which in these conditions can
разЕ5иг ;л1 с ii Ati.iee. Дл пред} .:режлеии iroro дальнейшего развити окраски, котора может уже достигнуть интенсивности, не соответс т в V10 Hie ii ксхч и ч е ству о 11 ) е дел емого марг нг(а, через 9-10 мин. от начала развити oKiKiCKH к онре,деленному раство1)у добавл ют 0,5 мл -1() (1-го раствора формалина. Пос.че этого окраска ислытуемого раствора сравниваетс с ок) эталон1П)1. растворов.RazE5ig; L1 with ii Ati.iee. For the fore}.: The iroro further development of color, which can already reach intensity, does not correspond to Vx Hie ii and xxh and a ratio of 11) e divisible marg ng (a, 9-10 min from the beginning of the development of oKiKiCKH 0.5 ml -1 () (1st formalin solution is added to the liquid divided by solution1). After this, the color of the solution to be treated is compared to ca. standard1P) 1. solutions.
Г1 j) и м е J) 2. Олределе гне Мп в приеутетвии катиона Ре .Г1 j) и ме J) 2. Alredele rah Mn in the preutuetvia of the cation of Fe.
Ана.шзнруемын нейтральный раствОр , содержащиГ 0,25-0,5 г солей н.1елочны. мета.тлов-0,5 ; - 8 7 Мп и око.чо 50 у Рё, номен;а1ОТ в пробирку бесцветного стекла, прибав,п ют 1 мл 10 ii-Hoio раствора .х.юристого аммони , 0,5 мл 10 -ного раствора с.егнетовон соли, и добавкой воды довод т объем до 5 мл. Одновре.менно готов т нжалу эталонных растворов, дл чего в н ть таки.х же пробирок ввод т соответственно 0,57, 1у. -{, Ч:, и 87 Мп но 1 мл раствора хло)истогч) аммони , по 0,5 мл сегнетовой соли, и обтаем во всех нробирках довод т до 5 мл. К нснытуе.мому )аствору и в эталонные растворы ввод т но четыре канли 0,05 и-ного сниртового раствора реактива и, носле неремегнивани , но 0,15 мл 20:п-норо раствора едкого натра. Через 9-10 мин. нрибавл ют, по, возможности одновременно во вес растворы, 0,3 мл 40:и-ног() раствора формалина. .;Ana neutralized neutral solution containing 0.25–0.5 g of salts of n.1 acid. meta.tl-0,5; - 8 7 Mp and about 50 yr of Ryo, nomen; a1OT into a test tube of colorless glass, adding 1 ml of 10 ii-Hoio solution of x.hour ammonium solution, 0.5 ml of 10% solution of ferocaine salt, and add water to 5 ml. Simultaneously, standard solutions are prepared, for which purpose, respectively, 0.57, 1y are introduced into the same tubes. - {, H :, and 87 Mp but 1 ml of chloro-istocch ammonium solution, 0.5 ml of segnetova salt each, and we put it in all bottles to 5 ml. To the solution, to the solution, four channels of a 0.05% solution of the reagent were added to the reference solutions and, but unreacted, but 0.15 ml of 20: p-noro caustic soda solution. After 9-10 min. If possible, at the same time, in the weight of the solution, 0.3 ml of 40: i-leg () formalin solution is added. ;
В нредложенных услови х можно проводить опреде.тение марганцаUnder the conditions proposed, manganese can be determined.
в растворах сернокислых, in sulphate solutions,
азотнокис .пых и хлористых солей кали , и аммони .nitrous oxide and potassium chloride salts, and ammonium.
В надсернокис.1ых со.т х In nadsernokis.1kh so.t x
ншлочных м-еталлов опреде.тение марганца вoз.oжнo single-metal metals determination of manganese is possible
Hoc.ie не)евода их в сернокис.чые.Hoc.ie not) evoda them in erythrocyte.
П р е д мет из о б р е т е н и PREDAM OF ABOUT THIS
Способ определени малых количеств двухвалентного марганца носредством окие.тительно-восстановнтельнон реакции, отличающийс тем, что, с це.1ью проведени анализа в присутствии небольших количеств железа, онреде.тение -производ т нос)едством |№акцфп с еа .1ицила.115-орто-а.минофено.1ом.The method of determining small amounts of bivalent manganese by means of opioid. Restoratively reducing reactions, characterized in that, with the purpose of conducting an analysis in the presence of small amounts of iron, it is necessary to carry out an analysis of the body. ortho-a.minofen.1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU44.3831A SU95772A1 (en) | 1951-02-23 | 1951-02-23 | Method for determination of small amounts of divalent manganese |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU44.3831A SU95772A1 (en) | 1951-02-23 | 1951-02-23 | Method for determination of small amounts of divalent manganese |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU95772A1 true SU95772A1 (en) | 1952-11-30 |
Family
ID=48370760
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU44.3831A SU95772A1 (en) | 1951-02-23 | 1951-02-23 | Method for determination of small amounts of divalent manganese |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU95772A1 (en) |
-
1951
- 1951-02-23 SU SU44.3831A patent/SU95772A1/en active
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