JPH0750027B2 - How to create basic data for computer color matching - Google Patents
How to create basic data for computer color matchingInfo
- Publication number
- JPH0750027B2 JPH0750027B2 JP20105389A JP20105389A JPH0750027B2 JP H0750027 B2 JPH0750027 B2 JP H0750027B2 JP 20105389 A JP20105389 A JP 20105389A JP 20105389 A JP20105389 A JP 20105389A JP H0750027 B2 JPH0750027 B2 JP H0750027B2
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- Japan
- Prior art keywords
- tissue
- basic data
- dye
- color matching
- tissues
- 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 - Lifetime
Links
- 230000003287 optical effect Effects 0.000 claims description 34
- 238000004043 dyeing Methods 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 16
- 239000000975 dye Substances 0.000 description 33
- 230000003595 spectral effect Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000008520 organization Effects 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 238000012935 Averaging Methods 0.000 description 1
- 238000010016 exhaust dyeing Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007447 staining method Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Spectrometry And Color Measurement (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は、コンピュータ・カラー・マッチングにおける
配合処方計算の基準となる基礎データの作成方法に関す
るものである。TECHNICAL FIELD The present invention relates to a method of creating basic data which serves as a reference for formulation prescription calculation in computer color matching.
(従来の技術) コンピュータ・カラー・マッチング(以後CCMと称す)
方法とは、目的の繊維組織を個々の染料単品で数段階の
濃度を染色し、そのサンプルの分光反射率から計算する
光学濃度を基礎データとし、この基礎データを任意の染
料の組合せで加算する事により目標色の光学濃度と一致
させる方法である。この方法は染色の未熟練者でも簡単
に短時間で色合わせが可能であり便利である。(Prior Art) Computer Color Matching (hereinafter referred to as CCM)
The method is to dye the target fiber tissue with individual dyes at several levels of density, and use optical density calculated from the spectral reflectance of the sample as basic data, and add this basic data with any combination of dyes. This is a method of matching the optical density of the target color. This method is convenient because even an unskilled person can easily perform color matching in a short time.
このCCMに必要な基礎データは、組織(例えば平織とあ
や織)が異なれば、組織に対する個々の染料の染着率が
異なるため組織毎に作成しなければならない。すなわ
ち、日々の染色作業に用いる全染料の数と数段階(通常
3ないし5段階)の濃度数とその染料で染色する組織の
数を掛け合わせた数の基礎データ・サンプルがCCMの準
備作業として必要となる。The basic data required for this CCM must be created for each tissue because different dyes have different dyeing rates to different tissues (for example, plain weave and twill weave). In other words, the basic data sample, which is the number of all dyes used for daily dyeing work, the number of concentrations of several levels (usually 3 to 5 levels), and the number of tissues to be dyed with that dye, is used as CCM preparation work. Will be needed.
(発明が解決しようとする問題点) しかしながら、多品種小量生産が要求される今日では、
多種類の組織を同色で染色する場合が多く、基準組織以
外の染色現場で一度も染めたことのない組織(以後新組
織と称す)の色出し要求がある毎に基礎データサンプル
を作成しなければならずCCMの準備作業だけで多く時間
と手間を要するという問題があった。(Problems to be solved by the invention) However, in today's demand for high-mix low-volume production,
In many cases, many types of tissues are stained with the same color, and a basic data sample must be created every time there is a request for coloration of a tissue that has never been stained at a staining site other than the reference tissue (hereinafter referred to as a new tissue). There was a problem that it took a lot of time and effort just to prepare the CCM.
本発明は上述の問題点に鑑みてなされたものであって、
新組織に対しても簡単かつ効率的に基礎データを作成し
うるコンピュータ・カラー・マッチング用基礎データ作
成方法の提供をその目的とするものである。The present invention has been made in view of the above problems,
It is an object of the present invention to provide a method of creating basic data for computer color matching, which can easily and efficiently create basic data even for a new organization.
(問題点を解決するための手段) 上述の目的は、コンピュータ・カラー・マッチングのた
めの基準となる基礎データを作成するに際し、基準組織
については個々の染料単品ごとの複数の濃度別サンプル
を作成しその光学的データを測定して基礎データとし、
基準組織以外の組織については基準組織に対する染料の
染着率と基準組織以外の組織に対する染着率との関係を
表わす染着率係数を予め実験的に求め、この染着率係数
を基準組織の光学的データに乗ずる事で基準組織以外の
組織の光学的データを計算し基礎データとすることを特
徴とするコンピュータ・カラー・マッチング用基礎デー
タ作成方法により達成される。(Means for Solving Problems) The above-mentioned purpose is to prepare basic data as a reference for computer color matching, and to prepare a plurality of density-specific samples for each individual dye as a reference tissue. Then, measure the optical data to make the basic data,
For tissues other than the reference tissues, a dyeing ratio coefficient that represents the relationship between the dyeing ratio of the dye to the reference tissues and the dyeing ratio to the tissues other than the reference tissues was experimentally obtained in advance, and this dyeing ratio coefficient This is achieved by a method for creating basic data for computer color matching, which is characterized by calculating optical data of a tissue other than the reference tissue by multiplying the optical data to obtain basic data.
本発明を更に詳しく説明する。The present invention will be described in more detail.
新組織のコンピュータ・カラー・マッチング用基礎デー
タは次の様にして作成することができる。ここではA染
料、B染料、C染料の3種類を用い5段階の濃度段階別
サンプルの光学的データ例えば光学濃度を得る場合につ
いて第2図に基づき説明する。The basic data for computer color matching of the new organization can be created as follows. Here, the case where three kinds of A dye, B dye, and C dye are used to obtain optical data of a sample for each density step of 5 steps, for example, optical density will be described with reference to FIG.
(1) 先ず、基準組織(X)については、A染料、B
染料、C染料単品で5段階(濃度1〜5)を染色し(ス
テップ)、得られたサンプルを測色し(ステップ
)、分光反射率Rより光学濃度 (基準組織(X)でA染料単品で濃度1で染色した時の
光学濃度、以下同様), (2) 次に新組織(Y)と基準組織(X)をA染料、
B染料、C染料単品で1段階(例えば濃度3)のみ同浴
で染色し(ステップ)、得られたサンプルを測色し
(ステップ)、分光反射率より光学濃度を求め(ステ
ップ)、両者の光学濃度の関係を染着率係数Hで表わ
す(ステップ)。(1) First, regarding the reference structure (X), A dye, B
Dye and C dye alone are dyed in 5 steps (density 1 to 5) (step), and the color of the obtained sample is measured (step). (Optical density when dyed with a standard tissue (X) with A dye alone at a density of 1, the same applies below), (2) Next, the new structure (Y) and the reference structure (X) are the A dye,
Dyes B and C alone are dyed in the same bath for only one step (for example, density 3) (step), the color of the obtained sample is measured (step), and the optical density is determined from the spectral reflectance (step). The relationship between the optical densities is represented by the dyeing rate coefficient H (step).
然してA染料の基準組織(X)に対する新組織(Y)の
染着率係数HAは次の様に表わすことができる。 Therefore, the dyeing rate coefficient HA of the new structure (Y) with respect to the reference structure (X) of the dye A can be expressed as follows.
また、B染料の基準組織(X)に対する新組織(Y)の
染着率係数HBは次の様に表わすことができる。 Further, the dyeing rate coefficient H B of the new structure (Y) with respect to the reference structure (X) of B dye can be expressed as follows.
また、C染料の基準組織(X)に対する新組織(Y)の
染着率係数HCは次の様に表わすことが出来る。 The dyeing coefficient H C of the new structure (Y) with respect to the reference structure (X) of C dye can be expressed as follows.
(3) 新組織(Y)のA染料、B染料、C染料単品で
濃度1,2,4,5の光学濃度 (基準組織(Y)でA染料単品で濃度1で染色した時の
計算上の光学濃度、以下同様), は上記の染着率係数を用いて次の様に計算出来る(ステ
ップ)。 (3) Optical density of new dye (Y) A, B, and C dyes alone with a density of 1,2,4,5 (Calculated optical density when dyed with A dye alone at a density of 1 in the reference tissue (Y), the same applies hereinafter), Can be calculated as follows using the above dyeing rate coefficient (step).
A染料単品 B染料単品 C染料単品 これらのデータを基礎データとしてコンピュータ・カラ
ー・マッチングを行ない、任意の染料の組合せで加算す
ることにより目標色の光学濃度と一致させるのである。A dye only B dye only C dye only Computer color matching is carried out using these data as basic data, and the optical density of the target color is made to match by adding any combination of dyes.
(作用) 本発明は、基準組織以外の組織については、個々の染料
単品ごとの複数の濃度段階別サンプルは作成せず、例え
ば基準組織と基準組織以外の組織を個々の染料単品ごと
に1つの濃度で同浴で試染し、染め上がりの両者のサン
プルの光学濃度より基準組織に対する基準組織以外の染
着率係数を求め、この染着率係数により試染しなかった
他の濃度における光学的データを計算するようにしてい
るので、基準組織以外の組織については数多くのサンプ
ルを試染する必要がなく、基礎データの作成が簡単に行
ないうるようになる。(Function) The present invention does not prepare a plurality of concentration-level samples for each individual dye alone for tissues other than the reference tissue, and, for example, for the reference tissue and the tissues other than the reference tissue, one sample is prepared for each individual dye. The sample was dyed in the same bath at the same concentration, and the dyeing rate coefficient for the reference tissue other than the reference tissue was obtained from the optical densities of both dyed samples, and the optical data for other concentrations not sampled by this dyeing rate coefficient Is calculated, it is not necessary to sample a large number of samples for organizations other than the reference organization, and basic data can be easily created.
(実施例) 以下、実施例に基づいて本発明を詳細に説明する。(Examples) Hereinafter, the present invention will be described in detail based on Examples.
第1図は、本発明のコンピュータ・カラー・マッチング
法を実施するための装置を示している。(1)は物体の
分光反射率および分光透過率を測定する分光光度計であ
り、少なくとも波長400nm〜700nmの可視光領域を測定で
きる装置である。(2)はROM、RAM、磁気ディスク等の
記憶装置であり、基準組織の個々の染料単品ごとの複数
の濃度段階別サンプルの光学濃度、新組織の染着率係数
を用いて計算した光学濃度が記憶されている。(3)は
マイクロコンピュータ等の演算装置であり、分光光度計
(1)で測定された色サンプルのデータを用いて光学濃
度を得る作業や、染着率係数を計算する作業や、新組織
について染着率係数を用いて基準組織より光学濃度を算
出する作業を行なうものである。(4)はディスプレ
イ、プリンタ等の表示装置であり、求められた新組織の
光学濃度等を表示するものである。FIG. 1 shows an apparatus for implementing the computer color matching method of the present invention. (1) is a spectrophotometer for measuring the spectral reflectance and spectral transmittance of an object, and is an apparatus capable of measuring at least a visible light region of wavelength 400 nm to 700 nm. (2) is a storage device such as a ROM, a RAM, and a magnetic disk. The optical densities of a plurality of samples of each density step for each individual dye of the reference tissue and the optical density calculated using the dyeing coefficient of the new tissue. Is remembered. (3) is a computing device such as a microcomputer, for obtaining the optical density using the data of the color sample measured by the spectrophotometer (1), for calculating the dyeing rate coefficient, and for new structures It is the work of calculating the optical density from the reference tissue using the dyeing rate coefficient. (4) is a display device such as a display or a printer, which displays the required optical density of the new tissue.
次に具体例により本発明を具体的に説明する。Next, the present invention will be specifically described with reference to specific examples.
(1) 先ず基準組織(X)として下記の糸使いのパン
ティストッキング(ナイロン)を用い、下記の条件で染
色し、サンプルを得た。(1) First, a panty hose (nylon) using the following yarn was used as the reference structure (X) and dyed under the following conditions to obtain a sample.
(i) 被染色物 基準組織のパンティストッキング レッグ部 15d/5fケンネル糸 パンティー・トウ部 30d/8fウーリー糸 (ii) 染料及び濃度 Nylosan Yellow N−3RL(サンド(株)社製) 0.01,0.
05,0.1%owf Nylosan Blue E−GL(サンド(株)社製) 0.005,0.0
1,0.05,0.1%owf Nylosan Red E−BNL(サンド(株)社製) 0.01,0.03,
0.05,0.1%owf (iii) 染色方法:吸尽染色法(浴比1:30) 得られたサンプルのレッグ部を測色し、分光反射率より
光学濃度 (基準組織(X)でYellow N−3RL単品で濃度0.01%owf
で染色した時の光学濃度、以下同様), を求めた。結果を第1表〜第3表に示す。(I) Material to be dyed Pantyhose leg part 15d / 5f Kennel yarn of the standard tissue Panty / toe part 30d / 8f Woolly yarn (ii) Dye and concentration Nylosan Yellow N-3RL (Sand Co., Ltd.) 0.01,0.
05,0.1% owf Nylosan Blue E-GL (Sand Co., Ltd.) 0.005,0.0
1,0.05,0.1% owf Nylosan Red E-BNL (Sand Co., Ltd.) 0.01,0.03,
0.05,0.1% owf (iii) Dyeing method: exhaust dyeing method (bath ratio 1:30) The legs of the obtained sample are color-measured and the optical density is determined from the spectral reflectance. (With reference structure (X), Yellow N-3RL alone has a concentration of 0.01% owf
Optical density when stained with I asked. The results are shown in Tables 1 to 3.
(2) 次に新組織(Y)として下記の糸使いのサポー
トタイプのパンティストッキング(ナイロン)を用い、
上記基準組織のパンティストッキングと同浴で下記の条
件で染色し、サンプルを得た。 (2) Next, as the new structure (Y), the following type of support type panty hose (nylon) is used,
A sample was obtained by dyeing under the following conditions in the same bath as the pantyhose having the above-mentioned standard structure.
(i) 被染色物 (A) 基準組織 (1)と同様 (B) 新組織ののパンティストッキング (サポートタイプ) レッグ部 (20×13×13DCY)×13d/3f生糸 パンティー部 (20×30PCY)×30d/8fウーリー糸 トウ部 13d/3f生糸×30d/8fウーリー糸×70d/18fウー
リー糸 (ii) 染料及び濃度 Yellow N−3RL 0.01%owf Blue E−GL 0.05%owf Red E−BNL 0.01%owf (iii) 染色方法 (1)と同様 得られたサンプルのレッグ部を測色し、分光反射率より
新組織の光学濃度 を求めた、結果を第4表〜第6表に示す。(I) Material to be dyed (A) Same as standard tissue (1) (B) New tissue pantyhose (support type) Leg (20 × 13 × 13DCY) × 13d / 3f raw silk panty (20 × 30PCY) × 30d / 8f Woolly thread Toe 13d / 3f raw thread × 30d / 8f Woolly thread × 70d / 18f Woolly thread (ii) Dye and concentration Yellow N-3RL 0.01% owf Blue E-GL 0.05% owf Red E-BNL 0.01% owf (iii) Similar to staining method (1), the leg part of the obtained sample was color-measured and the optical density of the new tissue was determined from the spectral reflectance. The results obtained are shown in Tables 4 to 6.
尚、基準組織の光学濃度 は第1表〜第3表と同一であった。 The optical density of the reference tissue Was the same as in Tables 1 to 3.
然してYellow N−3RLの基準組織(X)に対する新組織
(Y)の染着率係数HYを光学濃度がもっとも大きい波
長とその前後の波長すなわち420nm,440nm,460nmの染着
率係数の平均で求めた。Thus Yellow N-3RL reference tissue new tissue to (X) (Y) color yield coefficient H Y optical density is the greatest wavelength and before and after the wavelength i.e. 420nm of, 440 nm, the average of color yield coefficient 460nm I asked.
すなわち 以上3点の平均HYは また、Blue E−GLの基準組織(X)に対する新組織
(Y)の染着率係数HBを光学濃度がもっとも大きい波
長とその前後の波長すなわち620nm,640nm,660nmの染着
率係数の平均で求めた。Ie The average H Y of the above 3 points is In addition, the dyeing coefficient H B of the new structure (Y) with respect to the reference structure (X) of Blue E-GL is the average of the wavelengths with the largest optical density and the wavelengths before and after that, that is, 620 nm, 640 nm, 660 nm. I asked for.
すなわち 以上3点の平均HBは また、Red E−BNLの基準組織(X)に対する新組織
(Y)の染着率係数HRを光学濃度がもっとも大きい波
長とその前後の波長すなわち520nm,540nm,560nmの染着
率係数の平均で求めた。Ie The average H B of the above 3 points is Further, Red E-BNL reference tissue new tissue to (X) (Y) color yield coefficient H R the optical density and largest wavelength before and after the wavelength i.e. 520nm of, 540 nm, the average color yield coefficient 560nm I asked for.
すなわち 以上3点の平均HRは (3) 新組織(Y)の下記の染料濃度 Yellow N−3RL 0.05,0.1%owf Blue E−GL 0.005,0.01,0.1%owf Red E−BNL 0.03,0.05,0.1%owf の光学濃度 は、上記の染着率係数を用いて次の様に計算した。Ie The average H R of three or more (3) The following dye concentrations of the new structure (Y) Yellow N-3RL 0.05,0.1% owf Blue E-GL 0.005,0.01,0.1% owf Red E-BNL 0.03,0.05,0.1% Optical density of owf Was calculated as follows using the above dyeing rate coefficient.
(4) 比較として、新組織(Y)を、下記の条件で染
色しサンプルを得た。 (4) For comparison, the new tissue (Y) was dyed under the following conditions to obtain a sample.
(i) 被染色物 新組織 (ii) 染料び濃度 Yellow N−3RL 0.05,0.1%owf Blue E−GL 0.005,0.01,0.1%owf Red E−BNL 0.03,0.05,0.1%owf (iii) 染色条件 (1)と同様 得られたサンプルのレッグ部を測色し、分光反射率より
光学濃度 を求めた。(I) New tissue to be dyed (ii) Dye concentration Yellow N-3RL 0.05,0.1% owf Blue E-GL 0.005,0.01,0.1% owf Red E-BNL 0.03,0.05,0.1% owf (iii) Staining conditions Similar to (1), the leg part of the obtained sample was subjected to color measurement, and the optical density was determined from the spectral reflectance. I asked.
(3)で得られた計算値 と(4)で得られた実測値 を比較した結果を第7表〜第9表及び第3図〜第5図に
示す。Calculated value obtained in (3) And the measured values obtained in (4) The results of the comparison are shown in Tables 7 to 9 and FIGS. 3 to 5.
第7表〜第9表及び第3図〜第5図から明らかなように
両者がほとんど一致していることがわかる。 As is clear from Tables 7 to 9 and FIGS. 3 to 5, it can be seen that the two are almost the same.
尚、実施例では染着率係数Hを光学濃度がもっとも大き
い波長とその前後の波長の染着率係数の平均で求めるよ
うにしたが、これに限定されず素材や染料の特性に応じ
て全体の染着率係数の平均を用いる等滴宜の方法を用い
ることができる。In the embodiment, the dyeing rate coefficient H is obtained by averaging the dyeing rate coefficients of the wavelength having the largest optical density and the wavelengths before and after it, but the present invention is not limited to this and the dyeing rate coefficient H is determined according to the characteristics of the material and the dye. A convenient method using an average of the dyeing rate coefficients of can be used.
次に本発明の精度を確認するために、本発明で求めた基
礎データによりコンピュータ・カラー・マッチングを行
なった。結果を第10図に示す。Next, in order to confirm the accuracy of the present invention, computer color matching was performed using the basic data obtained by the present invention. The results are shown in Fig. 10.
第10表から明らかなように色差上でも目視判定上でも本
発明で求めた基礎データによるコンピュータ・カラー・
マッチングは調色精度が十分である事がわかる。 As is clear from Table 10, the computer color based on the basic data obtained by the present invention on both the color difference and the visual judgment.
It can be seen that matching has sufficient toning accuracy.
(発明の効果) 以上詳述したように本発明のコンピュータ・カラー・マ
ッチング用基礎データ作成方法によれば、コンピュータ
・カラー・マッチングに必要な準備作業の手順が迅速に
行なわれるようになり、生産性が一段と向上する等、そ
の効果には極めて顕著なものがある。(Effects of the Invention) As described above in detail, according to the computer color matching basic data creation method of the present invention, the procedure of the preparatory work required for computer color matching can be quickly performed, and the production can be performed. The effect is extremely remarkable, such as the further improvement of the property.
第1図は本発明の方法を実施する装置を示すブロック
図、第2図は本発明の方法を説明するフローチャート、
第3図〜第5図は本発明の効果を示すために、光学濃度
を実際に染色したサンプルから求めたものと本発明の手
順により計算で求めたものとの精度比較図である。1 is a block diagram showing an apparatus for carrying out the method of the present invention, FIG. 2 is a flow chart for explaining the method of the present invention,
FIGS. 3 to 5 are accuracy comparison diagrams of the optical densities obtained from the actually dyed sample and those obtained by calculation according to the procedure of the present invention in order to show the effect of the present invention.
Claims (1)
の基準となる基礎データを作成するに際し、基準組織に
ついては個々の染料単品ごとの複数の濃度別サンプルを
作成しその光学的データを測定して基礎データとし、基
準組織以外の組織については基準組織に対する染料の染
着率と基準組織以外の組織に対する染着率との関係を表
わす染着率係数を予め実験的に求め、この染着率係数を
基準組織の光学的データに乗ずる事で基準組織以外の組
織の光学的データを計算し基礎データとすることを特徴
とするコンピュータ・カラー・マッチング用基礎データ
作成方法。1. When preparing basic data as a standard for computer color matching, a plurality of samples for each concentration of each individual dye is prepared for a standard tissue, and the optical data is measured to prepare the basic data. As data, for tissues other than the reference tissues, a dyeing ratio coefficient representing the relationship between the dyeing ratio of the dye to the reference tissues and the dyeing ratio to the tissues other than the reference tissues was experimentally obtained in advance, and this dyeing ratio coefficient was calculated. A method for creating basic data for computer color matching, characterized by calculating the optical data of a tissue other than the reference tissue as the basic data by multiplying the optical data of the reference tissue.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20105389A JPH0750027B2 (en) | 1989-08-01 | 1989-08-01 | How to create basic data for computer color matching |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20105389A JPH0750027B2 (en) | 1989-08-01 | 1989-08-01 | How to create basic data for computer color matching |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0363533A JPH0363533A (en) | 1991-03-19 |
| JPH0750027B2 true JPH0750027B2 (en) | 1995-05-31 |
Family
ID=16434616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20105389A Expired - Lifetime JPH0750027B2 (en) | 1989-08-01 | 1989-08-01 | How to create basic data for computer color matching |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0750027B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011095225A (en) * | 2009-11-02 | 2011-05-12 | Olympus Corp | Apparatus and method for processing image, and microscope system |
-
1989
- 1989-08-01 JP JP20105389A patent/JPH0750027B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0363533A (en) | 1991-03-19 |
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