JPH02223828A - Ultraviolet spectrophotometer - Google Patents
Ultraviolet spectrophotometerInfo
- Publication number
- JPH02223828A JPH02223828A JP4391789A JP4391789A JPH02223828A JP H02223828 A JPH02223828 A JP H02223828A JP 4391789 A JP4391789 A JP 4391789A JP 4391789 A JP4391789 A JP 4391789A JP H02223828 A JPH02223828 A JP H02223828A
- Authority
- JP
- Japan
- Prior art keywords
- light
- detecting element
- melanine
- dye
- section
- 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.)
- Pending
Links
Landscapes
- Investigating Or Analysing Materials By Optical Means (AREA)
- Photometry And Measurement Of Optical Pulse Characteristics (AREA)
Abstract
Description
【発明の詳細な説明】 (イ)産業上の利用分野 本発明は、紫外分光元度計に関する。[Detailed description of the invention] (b) Industrial application field The present invention relates to an ultraviolet spectrometer.
(ロ) 従来技術
例えば、従来の紫外分光元度計は、第2図に示す構成を
してい友。これは、光源より出射し几白色元を分光器で
分光し九単色元を試料溶液(元の吸収を示さない溶液に
は発色試薬をカロえて化学反応を起させ、発色させた溶
液)に当てて通過し九光束の光電測光を行い、試料溶液
中の目的成分を分析するものである。(b) Prior art For example, a conventional ultraviolet spectrophotometer has the configuration shown in Figure 2. This is done by separating the bright white elements emitted from a light source using a spectrometer, and applying the nine monochromatic elements to a sample solution (for solutions that do not exhibit the original absorption, a coloring reagent is added to cause a chemical reaction to develop a color). The target component in the sample solution is analyzed by photoelectric photometry of nine luminous fluxes passing through the sample solution.
入射元の強さ1.の単色光束が濃度C1長さ4の液層を
通過すると、元が吸収されてその強さが減少する。通過
した直後の光束の強度″t−1tとすればItと10の
間にっぎの関係が成り立ち、ランハート・ベールの法則
とよばれている。Strength of incident source 1. When a monochromatic light beam passes through a liquid layer of concentration C1 and length 4, the original is absorbed and its intensity decreases. If the intensity of the luminous flux immediately after passing through the light beam is ``t-1t'', then the following relationship holds between It and 10, which is called the Ranhart-Beer law.
gcj
It=Io・10 ・・・・・・・・・・φ・由…・
・・(1)ここで会は分子化合物の種類、波長により定
まる常数で吸光係数と呼ばれ試料濃度C= I M 。gcj It=Io・10 ・・・・・・・・・φ・Yu…・
(1) Here, the coefficient is a constant determined by the type of molecular compound and the wavelength, and is called the extinction coefficient, and the sample concentration C = IM.
1=1cmのときのeのIItモル吸光係数と呼ぶ。It is called the IIt molar extinction coefficient of e when 1=1 cm.
1tと10(D関係でl t / 1 o == t
f透過度、透過度を百分率で表わしたtX100=Tt
−透過バーセンの法則で表わすと、
人=e−c−1・・・・・・ ・ ・ (2)と
なり吸光度は試料溶液の濃度に比例する。1t and 10 (In relation to D, l t / 1 o == t
f transmittance, transmittance expressed as a percentage tX100=Tt
- Transmission Expressed by Barsen's law, person = e-c-1... (2) and the absorbance is proportional to the concentration of the sample solution.
0号 発明が解決しようとする問題点■従来は、測九
部(光源〜吸収セ/I/)と検出部<1gt出器か、ら
指示計)が一体となってい九ので装置全体が大がかりな
ものとなった。No. 0 Problems to be Solved by the Invention ■ Conventionally, the measuring section (light source to absorption center/I/) and the detection section <1gt output device to indicator) were integrated, so the entire device was large-scale. It became something.
■従来装置では、測定データを保存しようとすれば検出
器よりの出力をプリントアウトしこnを保存する以外に
方法がなかった。■With conventional equipment, the only way to save measurement data was to print out the output from the detector and save it.
■検出器には高価な7オトダイオードアレイを使用して
い友ので装置の値段が高かつ几。■The detector uses an expensive 7-diode array, making the device expensive and expensive.
■測光部だけ、あるいは検出部だけが故障し文とき装置
が一体となっていたので修理が困難であった。- Only the photometering section or the detection section broke down, making it difficult to repair because the reading device was integrated.
に)問題点を解決する几めの手段
本発明は、検出素子にメラニン色素で染色した素子音用
い検出する事を特徴とする。B) Elaborate means for solving the problem The present invention is characterized in that detection is performed using elemental consonants dyed with melanin pigment as a detection element.
ここで用いるメラニン色素で染色し几素子は例えばアガ
ロースゲルなどの基板上にメラニン色素で染色してなる
。The element used here is formed by staining with melanin on a substrate such as agarose gel.
メラニン色素は、日焼けの元凶になる色素で紫外光を良
く吸収し、本発明ではその紫外光が測定セルからの透過
光に該当する。すなわち本発明はまず試料が収容さnた
測定セルに紫外光を照射し、セルからの透過光ヶメラニ
ン色素に吸収させる。Melanin pigment is the cause of sunburn and absorbs ultraviolet light well, and in the present invention, the ultraviolet light corresponds to the transmitted light from the measurement cell. That is, in the present invention, a measurement cell containing a sample is first irradiated with ultraviolet light, and the transmitted light from the cell is absorbed by the melanin pigment.
メラニン色素への紫外光の吸収は、光照射の強度に応じ
て変化の割合が変わる。故に測定セμからの透過光強度
、すなわち試料成分の濃度値により紫外光の吸収の度合
が変わることになる。The rate of change in the absorption of ultraviolet light by melanin pigment varies depending on the intensity of light irradiation. Therefore, the degree of absorption of ultraviolet light changes depending on the intensity of the transmitted light from the measurement unit, that is, the concentration value of the sample component.
従って、メラニン色素の紫色光吸収割合を読出すことに
より試料成分の濃度値に換算できる。Therefore, by reading the violet light absorption percentage of melanin pigment, it can be converted into the concentration value of the sample component.
具体的にはメラニン色素からの紫外光吸収割合の続出し
は、光記録媒体(元カード)に元を照射し、記録部の反
射率や透過率変化を読んで電気信号に変換する市販の元
カード読出し装置が利用できる。Specifically, the successive increase in the absorption rate of ultraviolet light from melanin pigments can be confirmed by using a commercially available source that irradiates an optical recording medium (original card) with the source, reads the changes in reflectance and transmittance of the recording area, and converts it into an electrical signal. Card reader available.
(ホ)作用
メラニン色素で染色した素子は、分析情報をもった光を
検出し記録するので、測光部と検出部をこの素子によっ
て時間的にも機能的にも分断することができる。(e) Function The element dyed with melanin pigment detects and records light carrying analytical information, so the photometric section and the detection section can be separated both temporally and functionally by this element.
(へ)実施例
本発明の実施例を第1図に示す。1が光源部で重水素ラ
ングやタングステンラングが収容さnている。2,3.
4は平面および球面鏡であり5がグレーティング、6が
測定セルである。(f) Example An example of the present invention is shown in FIG. 1 is a light source section which houses a deuterium rung and a tungsten rung. 2,3.
4 is a plane and a spherical mirror, 5 is a grating, and 6 is a measurement cell.
光源部1からのjt、は2.4で反射さnてグレーティ
ング5に達し単色元となって測定セ/I/6に入射され
る。jt from the light source section 1 is reflected at 2.4, reaches the grating 5, becomes a monochromatic source, and enters the measurement center/I/6.
測定セ1v6からの透過光は検出素子部7に入る。The transmitted light from the measurement cell 1v6 enters the detection element section 7.
検出素子部7の構成は第3図に示す。The configuration of the detection element section 7 is shown in FIG.
7aが透明な部材からなる検出素子ホルダーで該ホルダ
ーは可動枠7bで保持さ九上下、左右に移動する。移動
により透過光の入射点が異なり違う地点で情報の記録が
できる。Reference numeral 7a denotes a detection element holder made of a transparent member, and the holder is held by a movable frame 7b and can be moved vertically and horizontally. By moving, the incident point of transmitted light changes and information can be recorded at different points.
移動は、パルスモータ(図示せず)とビニオン7Cの連
結により行う。なお、7dは固定枠、7eはホルダー引
き出し部である。Movement is performed by connecting a pulse motor (not shown) and a binion 7C. Note that 7d is a fixed frame, and 7e is a holder drawer.
検出素子8′frホ〃ダー7aに挿入するときは、図示
のようにホルダー引き出し部7e ’に把持して手前に
引けば良い。なお検出素子8は、長方形状のアガロース
ゲル全面にメラニン色素を染色してなる。When inserting the detection element 8'fr into the holder 7a, it is sufficient to hold it in the holder drawer part 7e' and pull it toward you as shown in the figure. The detection element 8 is formed by staining the entire surface of a rectangular agarose gel with melanin.
検出素子部7に達した透過光は、透過光強度(すなわち
試料成分のm度)に応じて検出素子o f(蜆収される
。The transmitted light that has reached the detection element section 7 is collected by the detection element 7 according to the intensity of the transmitted light (that is, the m degree of the sample component).
紫外光を吸収した検出素子8は、市販の元カード読出し
装置により吸収の割合を読み取り濃!fflに換算する
。なお、濃度値に換算する几めには、予め既知濃度の標
準試料を用いて検量線を作成しておく。The detection element 8 that has absorbed the ultraviolet light reads the absorption rate using a commercially available original card reading device. Convert to ffl. In addition, in order to convert into a concentration value, a calibration curve is created in advance using a standard sample with a known concentration.
1回の測定終了後、検出素子ホルダー全可動させて透過
光の入射点を変えntf1枚の検出素子で多数の測定値
(同一試料でも異なる試料でも良い)′?を得らnる。After completing one measurement, move the entire detection element holder to change the incident point of the transmitted light, and obtain multiple measured values (the same sample or different samples) with one ntf detection element. Get.
また、紫外光?吸収し之メラニン色素は、吸収していな
いメラニン色素と表面の状態が異なるので、異なった表
面の表面積より濃度を求めることができる。Also, ultraviolet light? Since the absorbed melanin pigment has a different surface condition than the unabsorbed melanin pigment, the concentration can be determined from the surface area of the different surfaces.
(ト)効果
本発明は、検出素子にメラニン色素で染色した素子を用
いているので、該素子を永久に保存しておけば測定デー
タを永久に保存したことになる。(g) Effects Since the present invention uses an element dyed with melanin as a detection element, if the element is stored forever, the measurement data is stored forever.
!!友、分析部と検出部全切り離しでき、分析部を主体
とする装置の小型化が可能となる。! ! Additionally, the analysis section and detection section can be completely separated, making it possible to downsize the device with the analysis section as its main component.
W!IJ1図は、本発明に係る元測定装置の全体図第2
図は従来装置の構成概略図、第3図は元カード部の詳細
図である。
1・・・光源部 5・・・グレーティング6・・・
測定セ/L/7・・・検出素子部牟3図W! Figure IJ1 is the second overall diagram of the original measuring device according to the present invention.
The figure is a schematic diagram of the configuration of a conventional device, and FIG. 3 is a detailed diagram of the original card section. 1... Light source part 5... Grating 6...
Measuring cell/L/7...Detection element section Fig. 3
Claims (1)
分光光度計。1. An ultraviolet spectrophotometer whose detection element is an element dyed with melanin pigment.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4391789A JPH02223828A (en) | 1989-02-23 | 1989-02-23 | Ultraviolet spectrophotometer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4391789A JPH02223828A (en) | 1989-02-23 | 1989-02-23 | Ultraviolet spectrophotometer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02223828A true JPH02223828A (en) | 1990-09-06 |
Family
ID=12677065
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4391789A Pending JPH02223828A (en) | 1989-02-23 | 1989-02-23 | Ultraviolet spectrophotometer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02223828A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6882875B1 (en) | 1997-09-29 | 2005-04-19 | Boston Scientific Corporation | Visible display for an interventional device |
US7302289B2 (en) | 1998-01-20 | 2007-11-27 | Scimed Life Systems, Inc. | Readable probe array for in-vivo use |
-
1989
- 1989-02-23 JP JP4391789A patent/JPH02223828A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6882875B1 (en) | 1997-09-29 | 2005-04-19 | Boston Scientific Corporation | Visible display for an interventional device |
US7302289B2 (en) | 1998-01-20 | 2007-11-27 | Scimed Life Systems, Inc. | Readable probe array for in-vivo use |
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