JPS6120850A - Production of standard liquid for simultaneous calibration of electrode for measuring sodium ion, potassium ion and calcium ion and ph - Google Patents

Production of standard liquid for simultaneous calibration of electrode for measuring sodium ion, potassium ion and calcium ion and ph

Info

Publication number
JPS6120850A
JPS6120850A JP14316884A JP14316884A JPS6120850A JP S6120850 A JPS6120850 A JP S6120850A JP 14316884 A JP14316884 A JP 14316884A JP 14316884 A JP14316884 A JP 14316884A JP S6120850 A JPS6120850 A JP S6120850A
Authority
JP
Japan
Prior art keywords
ion
added
standard solution
prescribed
amt
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP14316884A
Other languages
Japanese (ja)
Other versions
JPH0347707B2 (en
Inventor
Narihiro Oku
成博 奥
Takeshi Kono
猛 河野
Seiji Usui
臼井 誠次
Hiroaki Uematsu
植松 宏彰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Horiba Ltd
Original Assignee
Horiba Ltd
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 by Horiba Ltd filed Critical Horiba Ltd
Priority to JP14316884A priority Critical patent/JPS6120850A/en
Priority to CN 85104664 priority patent/CN1027925C/en
Publication of JPS6120850A publication Critical patent/JPS6120850A/en
Publication of JPH0347707B2 publication Critical patent/JPH0347707B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/4163Systems checking the operation of, or calibrating, the measuring apparatus
    • G01N27/4165Systems checking the operation of, or calibrating, the measuring apparatus for pH meters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

PURPOSE:To obtain stably a standard soln. having a highly accurate concn. by adding a prescribed amt. of HCl and tris(hydroxymethyl)aminomethane(Tris) to a mixture composed of a prescribed amt. each of NaCl, KCl and CaCO3. CONSTITUTION:The prescribed amt. each of NaCl, KCl and CaCO3 are put into a tank for prepn. and further a prescribed amt. of HCl is added thereto to complete the reaction CaCO3+2HCl CaCl2+H2O+CO2. Pure water is added thereto to prepare a prescribed amt. of a soln. mixture which is then thoroughly stirred to make uniform the concn. The prescribed amt. of Tris is dissolved in the pure water and is added under stirring into the tank. A surface active agent (for example, ''Toriton X-100'') is finally added thereto and the pure water is added to the soln. to make the entire amt. to the prescribed amt. The NaCl, KCl and CaCO3 which have less hygroscopicity are used as the reagent in the stage of adjusting the sodium ion, potassium ion and calcium ion to the prescribed concn. and therefore the stable and exact weighing is made possible.

Description

【発明の詳細な説明】 〔産業上の利用分舒〕 本発明は例えば血液中のナトリウムイオン、(以下、N
a+と表わす)、カリウムイオン(以下、K+と表わす
)、カルシウムイオン(以下、Ca+と表わす)及びp
H測定電極の同時校正用標準液の製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application] The present invention is directed to, for example, sodium ions (hereinafter referred to as N
a+), potassium ions (hereinafter referred to as K+), calcium ions (hereinafter referred to as Ca+), and p
The present invention relates to a method for producing a standard solution for simultaneous calibration of H measurement electrodes.

〔従来技術] 血液中のNa%に、Ca  の活量又は濃度及びpHを
測定する装置における各イオンの測定電極及びpH測定
電極は、定期的に当該電極に対し一定の既知値を示す標
準液によって校正する必要がある。
[Prior art] In an apparatus for measuring the activity or concentration and pH of Na% and Ca in blood, the measurement electrodes for each ion and the pH measurement electrode are periodically filled with a standard solution that shows a certain known value for the electrodes. It is necessary to calibrate by

従来Na+、K+、Ca+、pH測定電極を別々に校正
する標準液は市販されてはいるが、上記4成分lこ対応
する測定型iを同時に校正しうる標準液は実現しておら
ず、カルシウム感応性電極とpH電極の同時調整のため
の対照液(本願発明の標準液)があるのみであった(特
公昭56−35052号公報)。
Conventionally, standard solutions for calibrating Na+, K+, Ca+, and pH measurement electrodes separately are commercially available, but a standard solution that can simultaneously calibrate the corresponding measurement type i for the above four components has not been realized. There was only a control solution (standard solution of the present invention) for simultaneous adjustment of a sensitive electrode and a pH electrode (Japanese Patent Publication No. 56-35052).

〔発明の目的〕[Purpose of the invention]

そこで、本発明の目的はNa”、K+、Ca+Elびp
H測定電極を同時校正する標準液を製造する新規かつ有
用な方法を提供することを目的とする。
Therefore, the purpose of the present invention is to
The purpose of the present invention is to provide a new and useful method for producing a standard solution for simultaneous calibration of H measurement electrodes.

〔実施例〕〔Example〕

標準液の調整に用いる試薬は、塩化ナトリウム(以下、
NaC1と表わす)、塩化カリウム(以下、Me’t′
と表わす)、炭酸カルシウム(以下、Ca COBと表
わす)、トリス(ヒドロキシメチル)アミノメタン(以
下、Trisと略す)、塩酸(以下、HCl  ト褒’
t)す)、及び界面活性剤として作用するトリトンX−
100(商品名)であり、これらの試薬はいずれも市販
の特級品を用いるのが好ましい。
The reagent used to prepare the standard solution is sodium chloride (hereinafter referred to as
(hereinafter referred to as NaC1), potassium chloride (hereinafter referred to as Me't')
Calcium carbonate (hereinafter referred to as Ca COB), tris(hydroxymethyl)aminomethane (hereinafter referred to as Tris), hydrochloric acid (hereinafter referred to as HCl)
t)), and Triton X- acting as a surfactant.
100 (trade name), and it is preferable to use commercially available special grade products for all of these reagents.

NaCl%KCl%Caco8については、110’C
で6時間以上加熱乾燥した後、デシケータ中で放冷した
ものを使用するのが望ましい。又、HcI! は予めフ
ァクターを小数点以下3桁まで求めた1規定溶液を使用
する。なお、調整時に使用する純水は、導電率lX10
−7Ω−1a−1以下のイオン交換水とする。
For NaCl%KCl%Caco8, 110'C
It is desirable to use a product that has been heated and dried for at least 6 hours and then allowed to cool in a desiccator. Also, HcI! Use a 1N solution whose factor has been determined in advance to three decimal places. Note that the pure water used during adjustment has a conductivity of 1×10
-7Ω-1a-1 or less ion-exchanged water.

上記した試薬の濃度及びpH値は第1表の通りである。The concentrations and pH values of the above reagents are shown in Table 1.

第    1    表 り標準液(洗浄液)、H標準液ともトリトンX−100
は10ppm である。
1. Both the surface standard solution (cleaning solution) and H standard solution are Triton X-100.
is 10 ppm.

次にL標準液、H標準液の作製手順の一例を数値ととも
に説明する。なお、調整量は50/とする。
Next, an example of the procedure for preparing the L standard solution and H standard solution will be explained along with numerical values. Note that the adjustment amount is 50/.

(1)L標準液、洗浄液 NaCl!(m、 w、 58.44.) 350.6
40±0.005p、KCl(m、 w、 74.56
 )14.912±0.001F?、Ca COB(m
、w、100.09)’6.005±0.001 yを
調整用タンクに入れ、さらにl規定I(Cl7(0,9
95(f(1,005)1885±0.IWd!を加え
、CaCO3+2HC1−CaC12+H20+CO2
↑なる反応を完結させる。そして更に、前記タンクに純
水を加えて総見が301の混合液を作製し、これを十分
に撹拌して、上記各試薬を溶解して一様な濃度の混合液
を作製する。
(1) L standard solution, cleaning solution NaCl! (m, w, 58.44.) 350.6
40±0.005p, KCl (m, w, 74.56
)14.912±0.001F? , Ca COB(m
, w, 100.09)'6.005±0.001 y is placed in the adjustment tank, and further l regulation I (Cl7(0,9
Add 95(f(1,005)1885±0.IWd!, CaCO3+2HC1-CaC12+H20+CO2
↑ Complete the reaction. Further, pure water is added to the tank to prepare a mixed solution with a total weight of 301, and this is sufficiently stirred to dissolve each of the above reagents to prepare a mixed solution with a uniform concentration.

そして、Tris(m、w、121.14)302.8
5±o、oospを約21の純水で溶解してTris水
溶液となし、このTris水溶液を前記タンク内に撹拌
しながら加える。上記においてTrisを一旦純水で希
釈しているのは% Trisはアルカリ性であり、濃度
の高い状態で加えると、タンク内の混合液と反応して沈
澱物を生ずるからである。
And Tris (m, w, 121.14) 302.8
5±o, oosp is dissolved in approximately 21% pure water to make a Tris aqueous solution, and this Tris aqueous solution is added into the tank with stirring. The reason why Tris is once diluted with pure water in the above is that % Tris is alkaline and if added at a high concentration, it will react with the mixed solution in the tank and form a precipitate.

最後に、トリトンX−100の10%溶液を5、〇−添
加し1更に純水を加えて全量が5olになるようにする
。このとき、トリトンX−100により溶液は非常に泡
立ちやすくなっているから、撹拌等については十分注意
を払う必要がある。
Finally, add 5,0-10% solution of Triton X-100 and add pure water to make the total volume 5 ol. At this time, since the solution becomes foamy very easily due to Triton X-100, it is necessary to pay sufficient attention to stirring and the like.

(II)  H標準液 H標準液の調整手順は、上述した(I)L標準液に準じ
て行なえばよいが、各試薬の混合量は以下の通りである
。即ち、 NaClCm、w、58.44)、、、、、、584.
400±0.005yKCI(m、w、74.56)、
、、、、、、、、、、、26.469±0.005yC
aCOa(m、w、100.09)、、、、12.76
2±0.001 y1規定H(J(0,995(f(1
,005)、、、 2325十0.1+++eTr i
 s (m、 w、 121.14 ) 、、、、 3
02.85±o、oo5yトリ)7X−100(10%
溶液)、、、、、、、、、、、、、、’5.0d上述の
ようにして、調整された各標準液は第2表に示す精度を
示すことが望ましい。
(II) H standard solution The procedure for preparing the H standard solution may be carried out according to the above-mentioned (I) L standard solution, but the mixing amounts of each reagent are as follows. That is, NaClCm, w, 58.44), , 584.
400±0.005yKCI (m, w, 74.56),
, , , , , , , , 26.469±0.005yC
aCOa (m, w, 100.09), , 12.76
2±0.001 y1 regulation H(J(0,995(f(1
,005),,, 232510.1+++eTri
s (m, w, 121.14) , , 3
02.85±o, oo5y bird) 7X-100 (10%
solution), , , , , , , , , , , '5.0d It is desirable that each standard solution prepared as described above exhibits the accuracy shown in Table 2.

第    2    表 トリトンx−iooについては、各液共に10±2 p
pm  とする。
Table 2 For Triton x-ioo, each solution was 10±2p
Let it be pm.

なお、調整後の標準液が第2表の精度を満たさないとき
は、適当に濃度補正を行うが、この濃度禎玉方法の詳細
については省略する。
Note that if the adjusted standard solution does not meet the accuracy shown in Table 2, the concentration is appropriately corrected, but the details of this concentration correction method will be omitted.

〔発明の効果〕〔Effect of the invention〕

以上の実施例から明らかなように、本発明においては、
Na s K s Ca  を所定濃度に調整するにあ
たって、試薬として吸湿性の少ないNaC1゜KCl、
CaC0Bを用いているので、安定して正確な秤量をす
ることができる。従って高精度の濃度を有する標準液を
安定して調製できる。特に、Ca COBは通常の方法
では溶けにくいが、吸湿性がなく、これをHC1!  
と反応させて水溶性の塩化カルシウムCCaC12) 
 として溶解させるようにしているので、より正確に安
定した標準液が得られる。
As is clear from the above examples, in the present invention,
When adjusting Na s K s Ca to a predetermined concentration, NaCl, which has low hygroscopicity, and 1° KCl are used as reagents.
Since CaC0B is used, stable and accurate weighing can be performed. Therefore, a standard solution having a highly accurate concentration can be stably prepared. In particular, Ca COB is difficult to dissolve using normal methods, but it is not hygroscopic, so it can be used as HC1!
Water-soluble calcium chloride CCaC12)
Since the standard solution is dissolved as a standard solution, a more accurate and stable standard solution can be obtained.

血液中のNa+、K+、Ca+、pH濃度の4成分を測
定するには正確に校正された測定電極を要するが、本発
明に係る標準液は上述の測定電極の同時校正用標準液と
して最適であるといえるものである。
Measuring the four components of Na+, K+, Ca+, and pH concentration in blood requires an accurately calibrated measurement electrode, and the standard solution according to the present invention is optimal as a standard solution for simultaneous calibration of the above-mentioned measurement electrodes. It can be said that there is.

自発手続補正書 1、事件の表示 昭和59年 特 許 頼第143168号2 発明の名
称  丹すウムイオン、カリウムイオン、カル/ラムイ
オン及び33、El、、tう7  ・0測定電′″i0
同”校11標準液09造雑事件との関係 特許出願人 4、代理人 5 補正命令の日付 6、 補正により増加する発明の数 7、補正の対象 明細書の発明の詳細な説明の欄 (1)  明細書第2頁第3行の「田測定電極」を「田
を測定する測定電極」と補正します。
Voluntary procedure amendment 1, indication of the case 1982 Patent Rei No. 143168 2 Title of the invention Tansuum ion, potassium ion, cal/lamb ion and 33, El, t7 ・0 measurement voltage'"i0
Relationship with the same school 11 standard solution 09 miscellaneous case Patent applicant 4, agent 5 Date of amendment order 6, number of inventions increased by amendment 7, column for detailed explanation of the invention in the specification subject to amendment ( 1) Correct "measuring electrode" in line 3 of page 2 of the specification to "measuring electrode for measuring".

(2)同第2頁第14行乃至第17行の「カルシウム−
公報)。」を次の通シ補正します。
(2) “Calcium-
Public bulletin). " will be corrected as follows.

「特公昭56−35052号公報に示すように、カルシ
ウム感応性電極と…電極の同時校正のための標準液があ
るのみであった。」 (3)同第3頁第6行乃至第9行の「トリス〜であり」
を次の通り補正します。
"As shown in Japanese Patent Publication No. 56-35052, there was only a standard solution for simultaneous calibration of calcium-sensitive electrodes and electrodes." (3) Page 3, lines 6 to 9 of the same. 's "Tris~de"
Correct as follows.

「トリス(ヒドロキシメチル)アミノメタン(化学式は
(HOCH2)3ONH2であシ、以下、’l’ris
と表わす)、塩酸(以下、HCtと表わす)、及び界面
活性剤として作用するトリトンX−100(商品名、化
学式はHO(CH2CH20)nC6H4C9H19で
ある)であり」 (4)同第4頁下から第14行の「L標準液〜とも」を
次の通り補正します。
"Tris(hydroxymethyl)aminomethane (chemical formula is (HOCH2)3ONH2, hereinafter 'l'ris
), hydrochloric acid (hereinafter referred to as HCt), and Triton X-100 (trade name, chemical formula is HO(CH2CH20)nC6H4C9H19) which acts as a surfactant.'' Correct "L standard solution~tomo" on line 14 as follows.

「なお、校正は通常2点校正(高濃度標準液と低濃度標
準液)によって行なわれるが、以下、高一度標準液をH
標準液、低濃度標準液をL標準液という。
"Calibration is usually performed by two-point calibration (high-concentration standard solution and low-concentration standard solution), but below, we will use the high-concentration standard solution with H
The standard solution and low concentration standard solution are called L standard solution.

L標準液(洗浄液)及びH標準液においてそれぞれ」For L standard solution (cleaning solution) and H standard solution respectively.

Claims (1)

【特許請求の範囲】 各々所定量の塩化ナトリウム、塩化カリウム及び炭酸カ
ルシウムを混合したものに、所定量の塩酸を加えて、 CaCO_3+2HCl→CaCl_2+H_2O+C
O_2↑なる反応が完結した混合液を作製し、更に所定
量のトリス(ヒドロキシメチル)アミノメタンを純水で
希釈したものを前記混合液に撹拌しながら加えた後、純
水を加えて全体として所定量となるようにしたことを特
徴とするナトリウムイオン、カリウムイオン、カルシウ
ムイオン及びpH測定電極の同時校正用標準液の製造方
法。
[Claims] A predetermined amount of hydrochloric acid is added to a mixture of predetermined amounts of sodium chloride, potassium chloride, and calcium carbonate, resulting in CaCO_3+2HCl→CaCl_2+H_2O+C
A mixed solution in which the reaction O_2↑ has been completed is prepared, and a predetermined amount of tris(hydroxymethyl)aminomethane diluted with pure water is added to the mixed solution while stirring, and then pure water is added to make the entire mixture. A method for producing a standard solution for simultaneous calibration of sodium ions, potassium ions, calcium ions, and pH measuring electrodes, characterized in that the standard solution is made to have a predetermined amount.
JP14316884A 1984-07-09 1984-07-09 Production of standard liquid for simultaneous calibration of electrode for measuring sodium ion, potassium ion and calcium ion and ph Granted JPS6120850A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP14316884A JPS6120850A (en) 1984-07-09 1984-07-09 Production of standard liquid for simultaneous calibration of electrode for measuring sodium ion, potassium ion and calcium ion and ph
CN 85104664 CN1027925C (en) 1984-07-09 1985-06-18 Method of preparing a standard solution for simultaneously calibrating electrodes for measuring sodium ions, potassium ions, calcium ions and the PH of a solution or dispersion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14316884A JPS6120850A (en) 1984-07-09 1984-07-09 Production of standard liquid for simultaneous calibration of electrode for measuring sodium ion, potassium ion and calcium ion and ph

Publications (2)

Publication Number Publication Date
JPS6120850A true JPS6120850A (en) 1986-01-29
JPH0347707B2 JPH0347707B2 (en) 1991-07-22

Family

ID=15332496

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14316884A Granted JPS6120850A (en) 1984-07-09 1984-07-09 Production of standard liquid for simultaneous calibration of electrode for measuring sodium ion, potassium ion and calcium ion and ph

Country Status (1)

Country Link
JP (1) JPS6120850A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0219769A (en) * 1988-05-13 1990-01-23 Instrumentation Lab Spa Ph analyzer and buffer solution system for standardization of electrolyte
WO2021181922A1 (en) * 2020-03-09 2021-09-16 日本特殊陶業株式会社 Calibration liquid for water quality measurement device, calibration-liquid-filled container for water quality measurement device, and calibration method using calibration liquid for water quality measurement device

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0219769A (en) * 1988-05-13 1990-01-23 Instrumentation Lab Spa Ph analyzer and buffer solution system for standardization of electrolyte
WO2021181922A1 (en) * 2020-03-09 2021-09-16 日本特殊陶業株式会社 Calibration liquid for water quality measurement device, calibration-liquid-filled container for water quality measurement device, and calibration method using calibration liquid for water quality measurement device
JP2021139837A (en) * 2020-03-09 2021-09-16 日本特殊陶業株式会社 Calibration solution for water quality measuring device, container containing calibration solution for water quality measuring device, and calibration method using calibration solution for water quality measuring device
CN115244393A (en) * 2020-03-09 2022-10-25 日本特殊陶业株式会社 Calibration solution for water quality measuring device, calibration solution container for water quality measuring device, and calibration method using calibration solution for water quality measuring device

Also Published As

Publication number Publication date
JPH0347707B2 (en) 1991-07-22

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