JP2524740B2 - Calibration method of PH meter - Google Patents

Calibration method of PH meter

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Publication number
JP2524740B2
JP2524740B2 JP62061634A JP6163487A JP2524740B2 JP 2524740 B2 JP2524740 B2 JP 2524740B2 JP 62061634 A JP62061634 A JP 62061634A JP 6163487 A JP6163487 A JP 6163487A JP 2524740 B2 JP2524740 B2 JP 2524740B2
Authority
JP
Japan
Prior art keywords
calibration
sheet
pure water
meter
solution
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.)
Expired - Fee Related
Application number
JP62061634A
Other languages
Japanese (ja)
Other versions
JPS63225163A (en
Inventor
晴夫 小谷
勝彦 冨田
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 JP62061634A priority Critical patent/JP2524740B2/en
Priority to KR1019870013846A priority patent/KR900005223B1/en
Priority to EP87118327A priority patent/EP0271102A3/en
Priority to CN89103431A priority patent/CN1012018B/en
Priority to CN87107352A priority patent/CN1010251B/en
Publication of JPS63225163A publication Critical patent/JPS63225163A/en
Priority to US07/291,628 priority patent/US4872956A/en
Application granted granted Critical
Publication of JP2524740B2 publication Critical patent/JP2524740B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、pH計の校正方法に関する。The present invention relates to a method for calibrating a pH meter.

〔従来の技術〕[Conventional technology]

pH計の電極の校正を行う場合、JIS規格によって調整
方法が規定された5種の標準緩衝溶液であって、25℃に
おけるpHがそれぞれ、1.68,4.01,6.86,9.18,10.02であ
る標準液が校正液として用いられている。
When calibrating the electrodes of a pH meter, there are five standard buffer solutions whose adjustment method is specified by JIS standards, and the standard solutions whose pH at 25 ° C are 1.68, 4.01, 6.86, 9.18, 10.02, respectively. Used as a calibration solution.

前記5種の標準緩衝溶液とは、シュウ酸塩標準液〔0.
05M四シュウ酸カリウムKH3(C2O4・2H2O水溶液〕、
フタル酸塩標準液〔0.05Mフタル酸水素カリウムC6H4(C
OOK)(COOH)水溶液〕、中性リン酸塩標準液〔0.025M
リン酸一カリウムKH2PO4−0.025Mリン酸二ナトリウムNa
2HPO4水溶液〕、ホウ酸塩標準液〔0.01Mホウ酸ナトリウ
ム(ホウ砂)Na2B4O7・10H2O水溶液〕、炭酸塩標準液
〔0.025M炭酸水素ナトリウムNaHCO3−0.025M炭酸ナトリ
ウムNa2CO3水溶液〕のことをいう。
The five standard buffer solutions are oxalate standard solutions [0.
05M tetrapotassium oxalate KH 3 (C 2 O 4) 2 · 2H 2 O aqueous solution],
Phthalate standard solution (0.05 M potassium hydrogen phthalate C 6 H 4 (C
OOK) (COOH) aqueous solution], neutral phosphate standard solution [0.025M
Monopotassium phosphate KH 2 PO 4 −0.025M Disodium phosphate Na
2 HPO 4 aqueous solution], borate standard solution [0.01 M sodium borate (borax) Na 2 B 4 O 7 · 10 H 2 O aqueous solution], carbonate standard solution [0.025 M sodium hydrogen carbonate NaHCO 3 -0.025 M carbonate Sodium Na 2 CO 3 aqueous solution].

そして、標準緩衝溶液の調整には、導電率が2×10-6
Ω-1cm-1(at 25℃)以下の純水が用いられ、例えば、
シュウ酸塩標準液は、四シュウ酸カリウム(JIS K847
4,pH測定用)12.71gを上記純水に溶解して11の溶液とす
るのである。
And to adjust the standard buffer solution, the conductivity should be 2 × 10 -6.
Pure water of Ω -1 cm -1 (at 25 ° C) or less is used.
The oxalate standard solution is potassium tetraoxalate (JIS K847
(4, pH measurement) 12.71 g is dissolved in the above pure water to make 11 solution.

第4図は、従来の校正方法の手順を示しており、同図
において、「保存」とは調整した標準液を上質のガラス
またはポリエチレンよりなる壜内に密閉するようにして
保存することであり、このようにして調整・保存された
標準液をセットとした校正液がpH計の付属品として市販
されている。
FIG. 4 shows the procedure of the conventional calibration method. In the figure, “preservation” means that the adjusted standard solution is sealed and stored in a bottle made of high quality glass or polyethylene. A calibration solution containing the standard solution thus adjusted and stored is commercially available as an accessory for the pH meter.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

ところで、pH計は校正時において最も精度よく計測が
行えるため、pH計測の際、その必要に応じて校正を行う
必要があり、上記校正液がpH測定において必要不可欠と
なるが、試験室内における計測時はともかく、屋外計測
や現場作業における計測の場合においては、上記セット
となった校正液や洗浄水をpH計とともに携行する必要が
あり、大変嵩高くなると云う欠点があるとともに、屋外
計測などにおいては校正作業がきわめて行いにくく、正
確に校正を行うのが困難であり、正確なpH測定を行う上
で障害となっていた。
By the way, since the pH meter can perform the most accurate measurement during calibration, it is necessary to calibrate it as necessary when measuring pH, and the above calibration solution is indispensable for pH measurement. Regardless of the time, in the case of outdoor measurement or measurement in the field work, it is necessary to carry the calibration solution and cleaning water set as above together with the pH meter, which has the drawback of being very bulky, and also in outdoor measurement etc. Was extremely difficult to calibrate, and it was difficult to calibrate accurately, which was an obstacle to accurate pH measurement.

本発明は、上述の事柄に留意してなされたもので、そ
の目的とするところは、携帯し易くかつ取り扱いが簡単
である校正用シートを用い、かつ、測定に際して簡易に
校正することができるpH計の校正方法を提供することに
ある。
The present invention has been made in consideration of the above matters, and its purpose is to use a calibration sheet that is easy to carry and easy to handle, and a pH that can be easily calibrated during measurement. It is to provide a calibration method for the meter.

〔問題点を解決するための手段〕[Means for solving problems]

上述の目的を達成するため、本発明に係るpH計の校正
方法は、校正用緩衝溶液を、イオン溶出のない化学的に
安定な吸水性を備えた吸水シートに吸収させた後、乾燥
させてなる校正用シートを、平面構造のpH電極に接触さ
せ、前記校正用シートに所定量の純水を滴下するように
して所定の校正を行うようにした点に特徴がある。
In order to achieve the above-mentioned object, the calibration method of the pH meter according to the present invention, the calibration buffer solution is absorbed into a water-absorbent sheet having chemically stable water absorption without ion elution, and then dried. The calibration sheet is characterized in that it is brought into contact with a pH electrode having a planar structure and a prescribed amount of pure water is dropped on the calibration sheet to perform a prescribed calibration.

〔作用〕[Action]

本発明に係るpH計の校正方法は、吸水シートに校正用
緩衝溶液を吸収させた後、乾燥した上記校正用シートを
平面構造のpH電極に載置して純水を校正用シートに滴下
させるだけの簡単な操作で校正を行うことができる。
The calibration method of the pH meter according to the present invention is such that after absorbing the calibration buffer solution in the water absorbing sheet, the dried calibration sheet is placed on the pH electrode having a planar structure and pure water is dropped on the calibration sheet. Calibration can be performed with just a simple operation.

その上、本発明では校正用緩衝溶液を上記校正用シー
トに吸収させている。そのため、上記校正用シートに滴
下される前記純水の量がある程度変化してもpH値は一定
となり、よって、前記純水を校正用シートに滴下させる
ときに前記純水の滴下量を厳密に軽量しなくてもよい。
要するに、校正用緩衝溶液を使用することで、前記純水
の滴下量の変動を許容でき、滴下操作を容易に行える。
Furthermore, in the present invention, the calibration buffer solution is absorbed in the calibration sheet. Therefore, the pH value is constant even if the amount of the pure water dropped on the calibration sheet changes to some extent, and therefore, when the pure water is dropped on the calibration sheet, the drop amount of the pure water is strictly adjusted. It does not have to be lightweight.
In short, by using the calibration buffer solution, it is possible to allow the fluctuation of the amount of the pure water to be dropped, and to easily perform the dropping operation.

〔実施例〕〔Example〕

以下、本発明の実施例を、第1図〜第3図を参照しな
がら説明する。
Hereinafter, an embodiment of the present invention will be described with reference to FIGS.

第1図は、本発明に係るpH計の校正用シートの製造か
らこの校正用シートを用いてpH計を校正するまでの各ス
テップを示し、例えばpH4およびpH7の校正用シートを例
に挙げて説明する。
FIG. 1 shows each step from the production of the calibration sheet for the pH meter according to the present invention to the calibration of the pH meter using this calibration sheet. For example, a calibration sheet for pH 4 and pH 7 is taken as an example. explain.

まず、フタル酸水素カリウム(JIS K8809,pH測定
用)を10.21g秤量するとともに、リン酸−カリウム(JI
S K9007,pH測定用)を3.40gをリン酸二ナトリウム(JI
S K9020,pH測定用)を3.55g秤量する(S1参照)。
First, weigh 10.21 g of potassium hydrogen phthalate (JIS K8809, for pH measurement) and add phosphate-potassium (JI
3.40 g of S K9007, for pH measurement) disodium phosphate (JI
Weigh 3.55 g of S K9020 (for pH measurement) (see S1).

次いで、上記フタル酸水素カリウム10.21gを導電率が
2×10-6Ω-1cm-1(at 25℃)以下の純水(以下、調整
用純水という)に溶解して11のフタル酸塩標準液を作
る。一方、上記リン酸−カリウム3.40gとリン酸二ナト
リウム3.55とを調整用純水に溶解して11の中性リン酸塩
標準液を作る(S2参照)。
Then, 10.21 g of the above potassium hydrogen phthalate was dissolved in pure water having an electric conductivity of 2 × 10 −6 Ω −1 cm −1 (at 25 ° C.) or less (hereinafter referred to as pure water for adjustment) to obtain 11 phthalic acid. Make a salt standard solution. On the other hand, 3.40 g of potassium-potassium phosphate and 3.55 of disodium phosphate are dissolved in pure water for adjustment to prepare 11 neutral phosphate standard solutions (see S2).

そして、上記フタル酸塩標準液と中性リン酸塩標準液
とをそれぞれ計量して、別々の容器に所定量入れる(S3
参照)。
Then, the phthalate standard solution and the neutral phosphate standard solution are weighed and put in separate containers in predetermined amounts (S3
reference).

次に、上記各容器内の標準液にそれぞれ吸収シートを
浸漬して、吸収シートに溶液を吸収させる(S4参照)。
Next, the absorbent sheet is immersed in the standard solution in each of the above-mentioned containers so that the absorbent sheet absorbs the solution (see S4).

ここで、吸収シートの素材としては、イオン溶出のな
い化学的に安定であって吸水性に富むものが好ましく、
例えば上記性質に加えて柔軟性に富み電極に対する密着
性が良好な高分子素材のほか、ガラスやセラミックファ
イバなどの無機素材でもよい。
Here, the material of the absorbent sheet is preferably one that is chemically stable without ion elution and rich in water absorption,
For example, in addition to the above-mentioned properties, in addition to a polymer material having high flexibility and good adhesion to an electrode, an inorganic material such as glass or ceramic fiber may be used.

本実施例では、セルロース100%の不織布(厚さ約220
μm)を吸収シートとして用いた。
In this example, a non-woven fabric made of 100% cellulose (having a thickness of about 220
μm) was used as an absorbent sheet.

次いで、上記のようにして標準液を吸収させた吸収シ
ートを室温で乾燥させて、pH4とpH7の校正用シート1,2
が得られる(S5および第2図参照)。
Then, the absorbent sheet that has absorbed the standard solution as described above is dried at room temperature, and the calibration sheets for pH 4 and pH 7 are used.
Is obtained (see S5 and FIG. 2).

この場合、水分の蒸発後、乾固した成分微粒子の粉末
が吸収シートから剥離しないように乾燥させることが大
切である。
In this case, after evaporation of water, it is important to dry the powder of the dried component fine particles so as not to be separated from the absorbent sheet.

上記のようにして得られた校正用シート1,2は、適宜
の包装を施して保存される(S6参照)。なお、これらの
校正用シート1,2は、他の標準液を吸収させた他の校正
用シートとともにセットされてpH計の付属品として市販
される。
The calibration sheets 1 and 2 obtained as described above are appropriately packaged and stored (see S6). It should be noted that these calibration sheets 1 and 2 are set together with other calibration sheets that have absorbed other standard solutions, and are commercially available as accessories for the pH meter.

そして、pH測定に際してpH計の電極を校正するには、
第3図に示すように、例えば本願出願人に係る特願昭61
−285371号において示される平面構造のpH電極3表面
に、上記校正用シート1(2)を密着するようにして載
置し、その上から、上記第1図におけるS2に示す調整用
純水の添加による標準液作成時に用いた調整用純水にほ
ぼ相当する量の純水4を滴下させる。この純水4の滴下
によって、校正用シート1(2)内では、再び、乾燥前
の標準液が得られ、この標準液によってpH電極の校正が
行われるのである。
And to calibrate the electrode of the pH meter when measuring pH,
As shown in FIG. 3, for example, Japanese Patent Application No.
-285371, the calibration sheet 1 (2) is placed in close contact with the surface of the pH electrode 3 having a planar structure, and the pure water for adjustment shown in S2 in FIG. Pure water 4 in an amount substantially equivalent to the pure water for adjustment used when the standard solution was prepared by addition is dropped. By dropping this pure water 4, the standard solution before drying is again obtained in the calibration sheet 1 (2), and the pH electrode is calibrated by this standard solution.

このように本実施例では、校正用シート1,2を平面構
造のpH電極3に載置して純水4を校正用シート1,2に滴
下させるだけの簡単な操作で校正を行うことができる上
に、校正用緩衝溶液を使用しているので、上記校正用シ
ートに滴下される前記純水の量がある程度変化してもpH
値は一定となり、よって、前記純水を校正用シートに滴
下させるときに前記純水の滴下量を厳密に計量しなくて
もよく、滴下操作を容易に行える。
As described above, in the present embodiment, the calibration sheets 1 and 2 can be calibrated by a simple operation of placing the calibration electrodes 1 and 2 on the planar pH electrode 3 and dropping pure water 4 onto the calibration sheets 1 and 2. In addition, since the calibration buffer solution is used, even if the amount of the pure water dropped on the calibration sheet changes to some extent, the pH
Since the value is constant, it is not necessary to strictly measure the dropping amount of the pure water when dropping the pure water on the calibration sheet, and the dropping operation can be easily performed.

そして、本実施例で用いたセルロース100%の不織布
よりなる吸収シートにより、上記標準液を吸収させて得
られた校正用シートを用いて上記平面構造のpH電極3の
校正を行ったところ、再現性および数日放置後の再現性
テストはいずれも良好であった。
The pH electrode 3 having the above-mentioned planar structure was calibrated by using the calibration sheet obtained by absorbing the standard solution with the absorbent sheet made of the non-woven fabric of 100% cellulose used in this example, and reproduced. And the reproducibility test after standing for several days were both good.

なお、pH標準緩衝溶液のうち、ホウ酸塩標準液および
炭酸塩標準液は、炭酸ガスを吸収してpHが著しく低下す
ることがあるので、これらの標準液を吸収シートに吸収
させて校正用シートを得る場合、吸収シートに標準液を
吸収させる工程から不活性ガス雰囲気内で処理を行うよ
うにし、乾燥や保存も大気に触れないようにするのがよ
い。
Of the pH standard buffer solutions, the borate standard solution and carbonate standard solution may absorb carbon dioxide gas and cause the pH to drop significantly, so absorb these standard solutions in an absorption sheet for calibration. When a sheet is obtained, it is preferable to carry out the treatment in an inert gas atmosphere from the step of absorbing the standard liquid in the absorbent sheet so that the sheet is not exposed to the atmosphere during drying and storage.

〔発明の効果〕〔The invention's effect〕

以上説明したように、本発明に係るpH計の校正方法
は、吸水シートに校正用緩衝溶液を吸収させた後、乾燥
した上記校正用シートを平面構造のpH電極に載置して純
水を校正用シートに滴下させるだけの簡単な操作で校正
を行うことができる。
As described above, the calibration method of the pH meter according to the present invention, after absorbing the calibration buffer solution in the water-absorbing sheet, the dried calibration sheet is placed on the pH electrode having a planar structure to obtain pure water. Calibration can be performed by a simple operation of simply dropping it on the calibration sheet.

その上、本発明では校正用緩衝溶液を上記校正用シー
トに吸収させている。そのため、上記校正用シートに滴
下される前記純水の量がある程度変化してもpH値は一定
となり、よって、前記純水を校正用シートに滴下させる
ときに前記純水の滴下量を厳密に計量しなくてもよい。
要するに、校正用緩衝溶液を使用することで、前記純水
の滴下量の変動を許容でき、滴下操作を容易に行える。
Furthermore, in the present invention, the calibration buffer solution is absorbed in the calibration sheet. Therefore, the pH value is constant even if the amount of the pure water dropped on the calibration sheet changes to some extent, and therefore, when the pure water is dropped on the calibration sheet, the drop amount of the pure water is strictly adjusted. You do not need to weigh.
In short, by using the calibration buffer solution, it is possible to allow the fluctuation of the amount of the pure water to be dropped, and to easily perform the dropping operation.

【図面の簡単な説明】[Brief description of drawings]

第1図〜第3図は本発明の一実施例を示し、第1図は本
発明に係るpH計の校正用シートの製造からこの校正用シ
ートを用いてpH計を校正するまでの各ステップを示すチ
ャート、第2図は上記校正用シートの一例を示す斜視
図、第3図は校正方法を説明するための図である。 第4図は従来技術を説明するためのチャートである。 1,2……校正用シート、3……平面構造のpH電極、4…
…純水。
1 to 3 show one embodiment of the present invention, and FIG. 1 shows each step from the production of the calibration sheet of the pH meter according to the present invention to the calibration of the pH meter using this calibration sheet. FIG. 2, FIG. 2 is a perspective view showing an example of the above calibration sheet, and FIG. 3 is a diagram for explaining the calibration method. FIG. 4 is a chart for explaining the conventional technique. 1,2 ... Calibration sheet, 3 ... Planar pH electrode, 4 ...
…Pure water.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】校正用緩衝溶液を、イオン溶出のない化学
的に安定な吸水性を備えた吸水シートに吸収させた後、
乾燥させてなる校正用シートを、平面構造のpH電極に接
触させ、前記校正用シートに所定量の純水を滴下するよ
うにして所定の校正を行うようにしたことを特徴とする
pH計の校正方法。
1. After absorbing a calibration buffer solution into a water-absorbing sheet having a chemically stable water-absorbing property without ion elution,
The dried calibration sheet is brought into contact with a pH electrode having a planar structure, and a predetermined amount of pure water is dropped onto the calibration sheet to perform a predetermined calibration.
Calibration method of pH meter.
JP62061634A 1986-12-11 1987-03-16 Calibration method of PH meter Expired - Fee Related JP2524740B2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP62061634A JP2524740B2 (en) 1987-03-16 1987-03-16 Calibration method of PH meter
KR1019870013846A KR900005223B1 (en) 1986-12-11 1987-12-04 Method of measuring ion-concentration and the like and a calibrating sheet as well as a calibrating method of measuring device used therein
EP87118327A EP0271102A3 (en) 1986-12-11 1987-12-10 Method for measuring the ion-concentration and the like, a calibrating sheet and a calibrating method for the measuring device used therefor
CN89103431A CN1012018B (en) 1986-12-11 1987-12-10 Scale plate of apparatus for measuring ionic concentration and like and scale method thereof
CN87107352A CN1010251B (en) 1986-12-11 1987-12-10 Method for measuring ion density and like, graduated piece and graduation of measurer used therein
US07/291,628 US4872956A (en) 1986-12-11 1988-12-29 Methods of measuring ion-concentration and the like and a calibrating sheet as well as a calibrating method of measuring devices used therein

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62061634A JP2524740B2 (en) 1987-03-16 1987-03-16 Calibration method of PH meter

Publications (2)

Publication Number Publication Date
JPS63225163A JPS63225163A (en) 1988-09-20
JP2524740B2 true JP2524740B2 (en) 1996-08-14

Family

ID=13176822

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62061634A Expired - Fee Related JP2524740B2 (en) 1986-12-11 1987-03-16 Calibration method of PH meter

Country Status (1)

Country Link
JP (1) JP2524740B2 (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55155962U (en) * 1979-04-24 1980-11-10
JPS61270650A (en) * 1985-05-24 1986-11-29 Matsushita Electric Works Ltd Reagent for quantitative determination of blood component and method for using said reagent

Also Published As

Publication number Publication date
JPS63225163A (en) 1988-09-20

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