Quantitative determination method of chemicals for processing semiconductor and an apparatus thereof

• US 5,097,130 A
• Filed: 09/19/1990
• Issued: 03/17/1992
• Est. Priority Date: 09/20/1989
• Status: Expired due to Term

• Current Assignee: Kurashiki Boseki Kabushiki Kaisha
• Original Assignee: Kurashiki Boseki Kabushiki Kaisha
• Inventors: Yanai, Naoki, Yokota, Hiroshi, Koashi, Katsue
• Primary Examiner(s): Fields, Carolyn E.
• Assistant Examiner(s): Dunn, Drew A.
• Application Number:
  US07/584,663
• Time in Patent Office: 545 Days
• Field of Search: 200/339, 200/341, 200/343, 200/338.4
• US Class Current: 250/339.09
• CPC Class Codes: G01N 2021/3174 Filter wheel
• CPC Class Codes: G01N 21/3577 for analysing liquids, e.g. polluted water
• CPC Class Codes: G01N 21/359 using near infrared light

Abstract

The present invention relates to a quantitative determination method of a medicament for processing semiconductor by near-infrared spectrometry at 800-1400 μm and an apparatus which is adapted to the practice of said method. According to the present invention, concentration of an aqueous solution of the medicament can be determined without drawbacks of the prior methods.

Claims

1. A method of determining quantitatively the concentration of an inorganic electrolyte in an aqueous solution used in processing a semiconductor and containing at least one inorganic electrolyte, said method comprising carrying out the following steps for each inorganic electrolyte:

(i) obtaining a near-infrared spectrum at 800-1400 nm of an aqueous solution of a known concentration of said electrolyte;

(ii) selecting from the spectrum obtained in step (i) at least three wavelengths at which there are observed significant differences between said spectrum and the near-infrared spectrum of pure water at 800-1400 nm, said differences being caused by ionic hydration;

(iii) repeating step (i) for a plurality of aqueous solutions each containing a known concentration of said electrolyte;

(iv) deriving a calibration equation (I) for said electrolyte by regression analysis of the relation between the concentration of electrolyte in the aqueous solutions used in steps (i) and (iii) and the absorbance at each of the wavelengths selected in step (ii);

space="preserve" listing-type="equation">C=Σ

α

.sub.i A.sub.i (I)

wherein C is the concentration of said electrolyte, A_i is the absorbance at each of said selected wavelengths, and α

_i is a constant determined for each of said selected wavelengths by said regression analysis;

(v) obtaining a near-infrared spectrum under the same conditions as in step (i) for a sample of unknown concentration of said electrolyte;

(vi) measuring the absorbance at each of said selected wavelengths in the spectrum obtained in step (v); and

(vii) determining the concentration of said electrolyte in the sample of unknown concentration by correlation between the absorbances measured in step (vi) and the calibration equation obtained in step (iv).

2. A quantitative determination method according to claim 1, wherein said inorganic electrolyte is any one or more of the electrolytes selected from the group consisting of a mixture of ammonia and hydrogen peroxide, a mixture of hydrochloric acid and hydrogen peroxide, a mixture of sulfuric acid and hydrogen peroxide, hydrofluoric acid, a mixture of hydrochloric acid and nitric acid, a mixture of hydrofluoric acid and ammonium fluoride, and sodium hypochlorite.