JPH01224089A - Method for adsorbing ionic dye dissolved in water - Google Patents
Method for adsorbing ionic dye dissolved in waterInfo
- Publication number
- JPH01224089A JPH01224089A JP63048299A JP4829988A JPH01224089A JP H01224089 A JPH01224089 A JP H01224089A JP 63048299 A JP63048299 A JP 63048299A JP 4829988 A JP4829988 A JP 4829988A JP H01224089 A JPH01224089 A JP H01224089A
- Authority
- JP
- Japan
- Prior art keywords
- dye
- dyeing
- water
- silica gel
- dissolved
- 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
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000000741 silica gel Substances 0.000 claims abstract description 27
- 229910002027 silica gel Inorganic materials 0.000 claims abstract description 27
- 239000002657 fibrous material Substances 0.000 claims abstract description 8
- 239000000975 dye Substances 0.000 claims description 48
- 238000001179 sorption measurement Methods 0.000 claims description 7
- 238000004043 dyeing Methods 0.000 abstract description 50
- 239000002351 wastewater Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 7
- 239000004753 textile Substances 0.000 description 7
- 238000007796 conventional method Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 238000010186 staining Methods 0.000 description 4
- 238000004065 wastewater treatment Methods 0.000 description 4
- 239000004744 fabric Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 210000003746 feather Anatomy 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000002759 chromosomal effect Effects 0.000 description 1
- 210000000349 chromosome Anatomy 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000010919 dye waste Substances 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Coloring (AREA)
- Water Treatment By Sorption (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、水中に溶解しているイオン性染料を繊維物質
によって吸着させる処理方法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a treatment method for adsorbing ionic dyes dissolved in water by textile materials.
従来の技術
繊維の染色工程から発生する染色残液すなわち染色廃水
は種々の染料が溶解しており、排水経路の河川湖沼海洋
を汚染させないためには高度の廃水処理が必要とされ、
BOD (生化学的酸素要求量)、COD (化学的酸
素要求旦)などで表示される汚染物質を除去してもなお
着色の問題が残り、高価な活性炭処理やオゾン酸化処理
などを余儀なくされている。Conventional technology The dyeing residue, or dyeing wastewater, generated from the textile dyeing process contains various dyes dissolved in it, and advanced wastewater treatment is required to prevent contamination of the rivers, lakes, marshes, and oceans along the drainage route.
Even after removing pollutants such as BOD (Biochemical Oxygen Demand) and COD (Chemical Oxygen Demand), the problem of coloration remains, and expensive activated carbon treatment and ozone oxidation treatment are forced. There is.
また一方、繊維物質の染色の工程においても短時間で吸
着効率のよい染色法が求められており、程々の染色助剤
が開発されてきたが必ずしも十分ではない、特に濃色の
染色を実施する場合には繊維物質に高濃度の染料を反応
吸着せしめねばならず、染液を新しく取り替えて数回染
色を繰り返さねばならない、したがって、染料を多量に
使用しなければらならず、このためにコスト高になる。On the other hand, there is also a need for a dyeing method that is quick and has high adsorption efficiency in the process of dyeing textile materials, and although some dyeing aids have been developed, they are not necessarily sufficient, especially when dyeing deep colors. In some cases, a high concentration of dye must be reacted and adsorbed onto the textile material, and the dyeing process must be repeated several times by replacing the dye liquor with a new one.Therefore, a large amount of dye must be used, resulting in high costs. become.
さらに、染色回数が多くなるために、その作業が煩雑で
ある。同時にまた染色廃水を多量に発生せしめ廃水処理
の負荷を大きくしていることにもつながっている。Furthermore, since the number of times of dyeing is increased, the work is complicated. At the same time, a large amount of dyeing wastewater is generated, increasing the burden of wastewater treatment.
発明が解決しようとする課題
本発明の目的は、上記の問題点に鑑み、所要の濃度の色
調の染色を効率よくしかも短時間で達成し、染色残液中
に未反応の染料の残存をほぼ0%にまで少なくすること
ができるとともに、従来方法での染色工程から発生する
染色廃水中に溶解残存する染料を廃水中から完全に除去
することができろ水中に溶解したイオン性染料の吸着処
理方法を提供することである。Problems to be Solved by the Invention In view of the above-mentioned problems, an object of the present invention is to efficiently achieve dyeing with a desired density of color in a short period of time, and to substantially eliminate unreacted dye from remaining in the dyeing residue. This is an adsorption treatment for ionic dyes dissolved in water, which can reduce the amount to 0% and completely remove dyes that remain dissolved in dyeing wastewater generated from dyeing processes using conventional methods. The purpose is to provide a method.
課題を解決するための手段
本発明は、イオン性染料を溶解した水中に溶解染料の重
量の3.5倍以上の量のシリカゲルを添加し、しかる後
、lJ! i、It重物質接触させることを特徴とする
水中に溶解したイオン性染料の吸着処理方法である。Means for Solving the Problems The present invention involves adding silica gel in an amount equal to or more than 3.5 times the weight of the dissolved dye to water in which an ionic dye is dissolved, and then adding lJ! This is a method for adsorption treatment of ionic dyes dissolved in water, characterized by bringing them into contact with heavy substances.
作 用
シリカゲルは従来から塗料、接着材、医薬品、化粧品な
どの分近において用いられるようになってきたが、その
特性を検討しiJI!、1と染料との反応に有効である
ことを発見したのである。勿論この場き、溶解染料の約
3,5倍以上のシリカゲルが共存することが必要である
ことを見出したのである。Function Silica gel has long been used in paints, adhesives, pharmaceuticals, cosmetics, etc., but we have studied its characteristics and iJI! , 1 was found to be effective in the reaction with dyes. Of course, in this case, it was found that it was necessary to coexist approximately 3.5 times more silica gel than the dissolved dye.
本発明は、1Jli tlt物質をイオン性染料で染色
する場きに所要の色調濃度に着色、発色するに必要な染
料のヱ(染色された繊維物質中に含有される染料のJi
t)にほぼ等しい星の染料を染色液中に溶解し、その染
料の重量の約3.5倍以上のシリカゲルを・染色液中に
添加する。しかる後、被染色体の繊維物資を上記のごと
<’A製された染色液によって処理する0本発明の方法
によれば、染色液中に溶解されている染料は短時間でほ
ぼ全量繊維物質に吸着され、染色残液中にはほとんど染
料は残存せず無色に近い透明液となり、わずかにシリカ
ゲルの白い沈澱、すなわちいわゆるホワイトカーボンが
残るのみである。The present invention provides a method for dyeing a 1Jli tlt material with an ionic dye, which is necessary for coloring and developing a desired color tone density.
A star dye approximately equal to t) is dissolved in the dyeing solution, and silica gel in an amount of about 3.5 times the weight of the dye or more is added to the dyeing solution. Thereafter, the chromosomal textile material is treated with the dyeing solution prepared as described above.According to the method of the present invention, almost all of the dye dissolved in the dyeing solution is converted into the textile material in a short period of time. After adsorption, almost no dye remains in the dyeing residue, resulting in a nearly colorless transparent liquid, with only a slight white precipitate of silica gel, ie, so-called white carbon, remaining.
また本発明は、従来方法による染色廃水にその廃水中に
溶存する染料の推定ffl量の3.5倍以上のシリカゲ
ルを添加攪拌して後、羊毛、絹またはナイロンおよびア
クリルならびに木綿またはセルローズ等の!!11維物
質全物質した容器の中に導入し、染色廃水と繊ti物質
とを接触させる。染色廃水中に溶解する染料は上記繊t
+fi群と短時間で反応し、廃水中の染料は完全に除去
される。染色廃水中に含有される染料の種類が判然とし
ている場きは、その8Mの染↑1と反応するm維のみを
泗択すればよい、廃水処理速度を高めるためには、染色
廃水を加熱昇温すればよい。In addition, the present invention involves adding and stirring silica gel in an amount of 3.5 times or more of the estimated amount of dye dissolved in the wastewater to the dyeing wastewater produced by the conventional method, and then dyeing wool, silk, nylon, acrylic, cotton, cellulose, etc. ! ! 1. Introduce all fiber materials into a container and bring the dyeing wastewater into contact with the fiber materials. The dye that dissolves in dyeing wastewater is the above-mentioned fiber t.
It reacts with the +fi group in a short time and the dye in the wastewater is completely removed. If the type of dye contained in the dyeing wastewater is known, it is only necessary to select the m fibers that react with the 8M dye↑1.To increase the wastewater treatment speed, it is necessary to heat the dyeing wastewater. Just raise the temperature.
、シリカゲルはその表面に多くの水酸基があり、水に対
して強い親和性を有し、水酸基(−OH)やアミノ基等
の水素結き性の末端基を有する分子とは非常に容易に水
素結合を形成する。したがって、染料を有効に1lIl
維構成分子に反応させることができる。Silica gel has many hydroxyl groups on its surface and has a strong affinity for water, and it is very easy to bond with molecules that have hydrogen-bonding end groups such as hydroxyl groups (-OH) and amino groups. form a bond. Therefore, the dye is effectively 1lIl
It can be reacted with fiber constituent molecules.
本発明を実施するにあたっては、シリカゲルの平均粒子
径が1〜10ミクロンであることが望ましい、その理由
は、平均粒子径がこの範囲より大きくなり過ぎると、す
なわちシリカゲルの平均粒子径が10ミクロンを超える
と、溶解染料の繊維物資への吸収吸着効果が低下し、ま
た、平均粒子径がこの範囲より小さくなると、すなわち
シリカゲルの平均粒子径が1ミクロン未満であると、シ
リカゲルが繊維物質に残存し所期の効果を挙げることが
困難になるからである。In carrying out the present invention, it is desirable that the average particle size of the silica gel is 1 to 10 microns. If the average particle size is smaller than this range, that is, the average particle size of silica gel is less than 1 micron, the silica gel will remain in the textile material. This is because it becomes difficult to achieve the desired effect.
また本発明では、表面上の水酸基が2.5〜3%以上を
有するシリカゲルを用いるのが盟ましく、2.59g以
下であると本発明の効果を挙げることができないことが
本件発明者によって確認された。In addition, in the present invention, it is preferable to use silica gel having 2.5 to 3% or more of hydroxyl groups on the surface, and the inventor has found that the effect of the present invention cannot be achieved if the amount is 2.59 g or less. confirmed.
染色に使用する染料ならびに廃液処理対象の染料によっ
て、使用するシリカゲルの表面上の水酸基を1T機物あ
るいは無機物によって必要に応じて処理するいわゆるマ
スキング処理によって添加する染液のFI H調整にも
役立ち、−層重発明の効果な高めることができるのであ
る。Depending on the dye used for dyeing and the dye to be treated as waste liquid, the hydroxyl groups on the surface of the silica gel used are treated with 1T organic or inorganic substances as necessary.It is also useful for adjusting the FIH of the dye solution added by so-called masking treatment. - The effectiveness of the layered invention can be increased.
本発明の実施に使用されるシリカゲルの価格は、−mの
染料のi格に比し10分の1を下まわり、シリカゲルを
染料の重量の3.5倍以上使用しても染色原′Flコス
トは従来法に比し、はるかに安価である。The price of the silica gel used in the practice of the present invention is less than one-tenth of the i rating of the -m dye, and even if silica gel is used at least 3.5 times the weight of the dye, the chromogen 'F The cost is much lower than conventional methods.
本発明は染料原単位の低減に有効であるのみならず、染
色工程の温度を従来法に比し、低い温度でも従来法以上
に染料の低減にも効果を発揮する。The present invention is not only effective in reducing the dye consumption per unit, but also exhibits an effect in reducing the amount of dye more than the conventional method even when the temperature of the dyeing process is lower than that of the conventional method.
さらに濃色染めの場合に従来法における2度染め、3度
染めなどを行なわなくても所望の濃度の染色を1回で短
時間で達成できるので生産性においても極めて浸れた方
法である。Furthermore, in the case of deep color dyeing, it is possible to achieve the desired density in a short time in one step without having to carry out double or triple dyeing as in conventional methods, so this method is extremely efficient in terms of productivity.
すなわち本発明方法を染色工程に採用すれば、■染料コ
ストの低減
■熱エネルギーの低減
■染色時間の可縮から生産性の向上
に卓効があり、
また染色工程から発生する排水中に残存する染料の旦が
ほとんどゼロであり、染色廃液による排水経路の汚染問
題を解消することができ、廃水処理工程をも極めて簡略
化することが可能であり、また(足来法による染色廃液
の廃水処理にも本発明の方法は残存染f1を完全に除去
することが可能になり、公害問題をも解消するのに大い
に(λ立つ。In other words, if the method of the present invention is adopted in the dyeing process, it will be extremely effective in reducing dye costs, reducing thermal energy, reducing dyeing time, and improving productivity. Since there is almost no dye waste, it is possible to solve the problem of contamination of the drainage route due to dyeing waste liquid, and it is possible to extremely simplify the wastewater treatment process. In addition, the method of the present invention makes it possible to completely remove the residual stain f1, which goes a long way toward solving the pollution problem.
本発明のπ様を実施例について説明すると次のとおりで
ある。The π pattern of the present invention will be explained with reference to an embodiment as follows.
実施例1
スミノールミリングブラックV L G (商品名)染
filを水に1526のOWFの濃度に溶解し平均粒子
径2,5ミクロンのシリカゲルを染y−1のff1mの
3.5倍の■を染fl溶解水に添加攪拌し、浴比1゛1
00で80℃の温度に調製し絹の羽二重を染色した。一
方、ブランクとしてシリカゲルを添加しない染iαを同
−条rトて7I製して染色した。Example 1 Suminol Milling Black V L G (trade name) dyeing film was dissolved in water to a concentration of 1526 OWF, and silica gel with an average particle size of 2.5 microns was dyed. Add to the dye fl solution water and stir to make a bath ratio of 1゛1.
The temperature was adjusted to 80° C. to dye silk habutae. On the other hand, as a blank, a dye iα to which no silica gel was added was prepared using the same strips as 7I and stained.
染色時間15分でブランクは青味の残る濃芸色であった
が本発明方法による場合はいわゆる烏の濡羽色と称され
る真黒であった。When the dyeing time was 15 minutes, the blank had a deep blue color with a tinge of blue, but when the method of the present invention was used, the color was pure black, which is called the so-called crow's feather color.
また双方の染色残液はブランクのそれが黒色で明らかに
染↑1の残存を示していたが、本発明方法による染色残
)αはほぼ無色透明でシリカゲルの白色沈澱の存在が;
2められた。In addition, for both staining residues, the blank was black and clearly showed the residual stain ↑1, but the staining residue α obtained by the method of the present invention was almost colorless and transparent, indicating the presence of white precipitates of silica gel;
I got hit twice.
実施例2
実施例1と同一の染1’lを用い、また被染色体に絹を
用いて本発明方法とシリカゲルご用いない方法(ブラン
ク)との染液の染TEI 濃度(OW F )と染色布
の色調濃度(K / S ) [K U B E L
K A −M U N Kの式により染色布の反射率
から計算した[]との関係を実験によって求めた結果は
、図面に示されるとおりである。Example 2 Using the same dye 1'l as in Example 1 and using silk as the chromosome, the dyeing TEI concentration (OW F ) and staining of the dye liquors of the method of the present invention and the method not using silica gel (blank) Cloth color density (K/S) [KUBEL
The relationship between [ ] calculated from the reflectance of the dyed cloth using the formula K A - M U N K was determined by experiment, and the results are as shown in the drawings.
すなわち、○W Fが5%の場合ブランクのIり/S(
図面の22参照)が7.5であるのに比し、本発明のK
/ S (図面のll参照)は18となり、染T1吸
収効率がはるかに高いことを示している。In other words, when ○WF is 5%, the blank I/S(
22 in the drawing) is 7.5, whereas the K of the present invention is 7.5.
/S (see ll in the drawing) was 18, indicating that the dye T1 absorption efficiency was much higher.
なお参考までに述べると、実施例1と同一のシリカゲル
を染料の重量の3.0倍以下の旦に設定した場合のK
/ S値は、図面の二点鎖線13に示されている。For reference, K when the same silica gel as in Example 1 is set at 3.0 times the weight of the dye or less.
/S value is indicated by the two-dot chain line 13 in the drawing.
実施例3
実施例1および実施1!1112のブランクにおいて用
いた場6の黒い染色残液は約61であった。この残液中
の染料)負度は0.12≦位と推定されるのでその残存
束石の量の約4倍のシリカゲルを残液中に添加した後に
、約4℃で加熱撹拌した。高さ50 c m直径5 c
mのガラス管中に絹糸を詰めて、このガラス管中と先
に調製した染色残iαを50 rnl/分の濃度で流下
させたところ、管から排出された水はぼ無色透明でiP
)つな。Example 3 The black dye residual liquid of field 6 used in the blanks of example 1 and run 1!1112 was about 61. Since the dye negativity in this residual liquid is estimated to be 0.12≦, approximately 4 times the amount of silica gel as the amount of residual slag was added to the residual liquid, and then heated and stirred at approximately 4°C. Height: 50 cm Diameter: 5 cm
Silk thread was stuffed into a glass tube of 1.0 m, and the previously prepared dyed residue iα was allowed to flow down the glass tube at a concentration of 50 rnl/min. The water discharged from the tube was almost colorless and transparent.
)tuna.
実施例Z1
実施例1において実施した方法において使用したシリカ
ゲルの平均粒子径2.5ミクロンのものと、平均粒子径
13ミクロンのシリカゲルな用いた場なひ比較したとこ
ろ、実施例1の場りは烏の濡羽色とri;される真黒で
、しったのに比し、平均粒子径13ミクロンのシリカゲ
ルを用いた場きは染色布に染色むらが散見され、また染
色濃度は若干藍色がかつており、染色残液は黒色を呈し
ており、染↑:lの!a維物質による吸収吸着効果が劣
ることが認められた。Example Z1 A comparison was made between the silica gel used in the method carried out in Example 1 with an average particle diameter of 2.5 microns and the silica gel with an average particle diameter of 13 microns. The color is pure black, which is similar to the color of a crow's wet feathers, and compared to Shishita, when silica gel with an average particle size of 13 microns was used, uneven dyeing was seen on the dyed cloth, and the dyeing density was slightly indigo. The staining residue is black, and the dyeing ↑:l! It was observed that the absorption and adsorption effect of the a-fiber material was poor.
発明の効果
以上のように本発明によれば、イオン性束王り1と繊維
′ll1I質との吸着反応効率を極めて著しく向上せし
める方法であり、染色工程における染料原単位の低下な
どと特に濃色染めにおける場合の従来の2度染め、3度
染めの繁雑さを解消し染色コストの低減に著しく効果を
発揮するのみならず、染色残液中の染〒4残存量をほと
んどなくし、公害対策における発生源対策としても潰れ
ている。また同じく詳述したように染色廃水の処理にも
卓効を有するものである。Effects of the Invention As described above, according to the present invention, there is provided a method that very significantly improves the efficiency of the adsorption reaction between the ionic bundle material 1 and the fiber material. Not only is it extremely effective in reducing dyeing costs by eliminating the complexity of conventional double and triple dyeing in color dyeing, but it also eliminates almost all the residual amount of dye 4 in the dyeing residue, which helps prevent pollution. It has also failed as a countermeasure for the source. Furthermore, as described in detail, it is also highly effective in treating dyeing wastewater.
図面は、実施例2の実験結果を示すグラフであり、1M
軸に染浴中の染料濃度(%0WF)、縦軸にK / S
値を示したものである。グラフ中の実線!1は本発明方
法、破線12はブランク、二点鎖線13は本発明のシリ
カゲルを染マ1の重量の3゜0倍以下の量に設定した場
合のK / S値をそれぞれを示している。
代理人 弁理士 西教 圭一部The drawing is a graph showing the experimental results of Example 2, and 1M
The axis is the dye concentration in the dye bath (%0WF), the vertical axis is K/S
It shows the value. Solid line in the graph! 1 indicates the method of the present invention, dashed line 12 indicates a blank, and chain double-dashed line 13 indicates the K/S value when the amount of silica gel of the present invention is set to be 3.0 times or less the weight of dye marker 1, respectively. Agent Patent Attorney Keiichi Nishikyo
Claims (1)
倍以上の量のシリカゲルを添加し、しかる後、繊維物質
と接触させることを特徴とする水中に溶解したイオン性
染料の吸着処理方法。3.5 of the weight of dye dissolved in water containing ionic dye
1. A method for adsorption treatment of ionic dyes dissolved in water, which comprises adding silica gel in an amount more than double the amount and then bringing it into contact with a fiber material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63048299A JPH01224089A (en) | 1988-02-29 | 1988-02-29 | Method for adsorbing ionic dye dissolved in water |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63048299A JPH01224089A (en) | 1988-02-29 | 1988-02-29 | Method for adsorbing ionic dye dissolved in water |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01224089A true JPH01224089A (en) | 1989-09-07 |
JPH0535036B2 JPH0535036B2 (en) | 1993-05-25 |
Family
ID=12799558
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63048299A Granted JPH01224089A (en) | 1988-02-29 | 1988-02-29 | Method for adsorbing ionic dye dissolved in water |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01224089A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0937972A (en) * | 1995-07-26 | 1997-02-10 | Hitoshi Akamine | Oil separation apparatus |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62117886A (en) * | 1985-11-19 | 1987-05-29 | 農林水産省蚕糸・昆虫農業技術研究所長 | Dyeing of fiber |
-
1988
- 1988-02-29 JP JP63048299A patent/JPH01224089A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62117886A (en) * | 1985-11-19 | 1987-05-29 | 農林水産省蚕糸・昆虫農業技術研究所長 | Dyeing of fiber |
Also Published As
Publication number | Publication date |
---|---|
JPH0535036B2 (en) | 1993-05-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Kurbus et al. | The study of the effects of the variables on H2O2/UV decoloration of vinylsulphone dye: part II | |
US5403362A (en) | Mordant and method of dyeing fibers | |
Mughal et al. | Dye fixation and decolourization of vinyl sulphone reactive dyes by using dicyanidiamide fixer in the presence of ferric chloride | |
KR970701285A (en) | Process for dyeing polytrimethylene terephthalate fibers and use of thus dyed fibers | |
CA2394349A1 (en) | Enzymatic method for textile dyeing | |
Senthilkumar et al. | Studies on the possibility of recycling reactive dye bath effluent after decolouration using ozone | |
Perkins et al. | Renovation of Dyebath Water By Chlorination or Ozonation. | |
JPH01224089A (en) | Method for adsorbing ionic dye dissolved in water | |
Lewis et al. | Modification of cotton with nicotinoyl thioglycollate to improve its dyeability | |
CN105084436B (en) | A kind of application of the recycle-water that efficient decolorizing of printing waste water obtains in printcloth washing process | |
CN112301763A (en) | Pure cotton fabric and dyeing method thereof | |
Saremi et al. | Dyeing of fibers and impact on the environment | |
DE59301994D1 (en) | METHOD FOR DYING AND PRINTING TEXTILE MATERIALS FROM CELLULOSE FIBERS IN THE PRESENCE OF CYCLIC ALPHAHYDROXYKETONES | |
Burkinshaw et al. | The aftertreatment of sulphur dyes on cotton | |
Chu et al. | Effects of uv‐decolouring of aromatic dyes with different chemical structures | |
FR2379645A1 (en) | TREATMENT OF DYED OR PRINTED TEXTILES WITH REACTIVE AND DISPERSION DYES | |
Vajpeyee et al. | Aspects of mordants and metal complex dyes | |
CN108467466A (en) | A kind of aluminum sulfate as catalyst prepares the method and its application of high viscosity dicandiamide-formaldehyde condensation polymer | |
CN114293386B (en) | One-bath one-step dyeing method for polyester-cotton fabric | |
JP4050801B2 (en) | Method for modifying polymer material by gas phase photochemical reaction, modified polymer material and dyeing method | |
Rattee | The colouring of textiles | |
JPH0797785A (en) | Method for printing with microorganism and microorganism for decoloring azo dyestuff | |
GB1597342A (en) | Treatment of aqueous effluents containing a dyestuff | |
CN109879351B (en) | Functional powder capable of being recycled, rapidly and efficiently purifying printing and dyeing wastewater, preparation method and decoloring method thereof | |
JPH0121265B2 (en) |