JPS6115182B2 - - Google Patents
Info
- Publication number
- JPS6115182B2 JPS6115182B2 JP55140495A JP14049580A JPS6115182B2 JP S6115182 B2 JPS6115182 B2 JP S6115182B2 JP 55140495 A JP55140495 A JP 55140495A JP 14049580 A JP14049580 A JP 14049580A JP S6115182 B2 JPS6115182 B2 JP S6115182B2
- Authority
- JP
- Japan
- Prior art keywords
- bleaching
- whiteness
- ammonia gas
- cloth
- hydrogen peroxide
- 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
Links
- 238000004061 bleaching Methods 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 22
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 19
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 18
- 239000000835 fiber Substances 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 5
- 229920003043 Cellulose fiber Polymers 0.000 claims description 3
- 238000011282 treatment Methods 0.000 claims description 3
- 239000004753 textile Substances 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 21
- 239000000243 solution Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 238000010025 steaming Methods 0.000 description 8
- 229920000742 Cotton Polymers 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000004115 Sodium Silicate Substances 0.000 description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 6
- 229910052911 sodium silicate Inorganic materials 0.000 description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 239000004202 carbamide Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid group Chemical class S(N)(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 3
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RBNPOMFGQQGHHO-UWTATZPHSA-N D-glyceric acid Chemical compound OC[C@@H](O)C(O)=O RBNPOMFGQQGHHO-UWTATZPHSA-N 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- -1 fatty acid alkali metal salt Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000004967 organic peroxy acids Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Description
本発明はセルロース繊維の過酸化水素スチ―ミ
ング漂白において、新規な漂白助剤を用いて漂白
する方法に関するものである。
従来のセルロース繊維の過酸化水素スチ―ミン
グ漂白、過酸化水素、ケイ酸ソーダ、アルカリ
剤、浸透剤を含む液を布にパツドし、これを100
℃前後の高温で蒸熱処理していた。このパツド液
のPHは10以上であり、ケイ酸ソーダが安定剤とし
て加えてはあるが、サチユレーター中で過酸化水
素が除々に分解するので1日以上の長時間一定の
過酸化水素の濃度を保持することは不可能であ
り、毎日パツド液を交換しているのが実状であ
る。またケイ酸ソーダの添加はいわゆるケイ酸塩
障害をひきおこすため決して望ましいことではな
い。その上高アルカリ、高温による処理は繊維を
疎剛にし、風合が低下する等の欠点があつた。
本発明の目的は上記の欠点を克腹する漂白法を
提供することにある。本発明の漂白方法は、ケイ
酸ソーダ、アルカリ剤を全く含まない中性付近の
PHのパツド液を繊維にパツドし、これをアンモニ
アガス処理及び70〜100℃で蒸熱することを特徴
とする。本発明の漂白方法によれば、パツド液は
中性に保たれるのでサチユレーター中のH2O2は
非常に安定に保たれる。また、70℃程度の漂白温
度でも十分な白度が得られるのでエネルギーコス
トの低減となり、その上、ケイ酸塩障害もない風
合の良好な製品が得られる。
H2O2による中性漂白については、従来からい
くつかの研究がなされている。例えば、特許公報
昭49―30234では尿素、ジアン酸塩、スルフアミ
ン酸及びスルフアミン酸塩の中から選ばれた一種
又は二種以上の物質と縮合リン酸塩とを使用する
方法が提案されている。又、特許公報昭49―
30235には、リン酸エステル及びリン酸エステル
から成る群から選ばれた物質と尿素、アミド、イ
ミド、ジアン酸塩、スルフアミン酸及びスルフア
ミン酸から成る群から選ばれた物質を併用する方
法が提案されている。しかしながらこれらの方法
は、H2O2の活性化については不十分でであり、
薄手の布にはある程度有効であるが、厚手の布の
漂白に適用すると漂白白度も低く、ネツプの除去
も不完全となる。過酸化水素の酸性漂白について
も特許公報昭50―34674に提案されている。これ
は乳酸、酒石酸、クエン酸、グリコール酸等のオ
キシカルボン酸と過酸化水素を併用し有機過酸を
生成せしめ、酸性で漂白する方法である。しか
し、この方法によれば、綿布の場合ネツプの除去
が非常に悪く、実際の漂白に適用することは無理
であろう。また、ケイ酸ソーダを含まないいわゆ
る非ケイ酸塩系の安定剤を使用する方法もいくつ
か提案されている。例えば、出願人がすでに提案
した特許公報昭50―10425には、脂肪酸アルカリ
士類金属塩と易溶性マグネシウム塩を使用する方
法が、また、特許公報昭50―34675には水可溶性
タンパク質を使用する方法等が記載されている。
しかし、これらの方法のうち前者はパツチ式の漂
白には効果を発揮するが、スチーミング漂白方法
の場合はケイ酸ソーダを使用した漂白方法と比較
して漂白効果は不十分である。また後者は、コス
ト的に問題がある。
しかるに、本発明における如く、過酸化水素及
びクエン酸塩を含む液を布にパツドし、アンモニ
アガスとともに蒸熱する漂白方法は、70℃程度の
温度でも漂白効果は著しく、厚手の布に対しても
十分適用できるものである。又、ケイ酸塩を全く
含まない非ケイ酸塩漂白方法であるので、そのメ
リツトは大きい。
易溶性クエン酸塩としては、ナトリウム塩、ア
ンモニウム塩、カリウム塩等が使用でき、クエン
酸塩の使用量は、溶液量に対して、0.05〜1.0
%、望ましくは、0.1〜0.3%である。0.05%以下
の添加量では効果がなく、0.1%以上添加しても
効果は変わらず、不経済となる。この場合、尿
素、総合リン酸塩の添加は、良い結果をもたらす
が、クエン酸塩以外の酒石酸塩、グリコール酸
塩、リンゴ酸塩、乳酸塩、グリセリン酸塩等のオ
キシカルボン酸塩類の添加は効果がない。
本発明における漂白方法の特徴は、また、蒸熱
時前又は、蒸熱中にアンモニアガスを使用するこ
とである。この場合、アンモニアガスをボンベよ
り直接スチーマー中に導入してもよいし、アンモ
ニア水をスチーマーの底部に保持し、蒸発により
スチーマー中に供給してもよい。他の一般的なア
ルカリ剤である。カセイソーダ、炭酸ソーダ、水
酸化カルシウム、炭酸カルシウム等は、ガス化す
ることが困難なため使用できない。アンモニアガ
スの供給量は繊維重量に対して0.1重量%〜20重
量%が適当である。0.1%以下のアンモニアガス
使用量では増白効果が得られず、20%以上の供給
量ではセンイの脆化が著しく、望ましくない。ア
ンモニアガス処理は、漂白液を繊維にパツド後に
一定時間アンモニアガスを供給し、その後蒸熱処
理する方法をとつてもよいし、蒸熱と同時に行う
方法でもよい。アンモニアは処理時必ずガス状で
なければならず、たとえばアンモニア水をパツド
液に添加した場合は、パツド液が当然アルカリ性
となりH2O2が不安定になるばかりでなく、パツ
ドした繊維の蒸熱処理を行つても漂白効果は小さ
い。
次に本発明を更に具体的に説明するために実施
例及び比較例をあげるが、これらは特に本発明を
限定するものではない。
実施例 1
35%(重量)過酸化水素溶液40g/、クエン
酸ソーダ(2水塩)2g/、ヘキサメタリン酸
ソーダ1g/、非イオン界面活性剤2g/を含
む水溶液を精練した40番手綿メリヤス布に充分浸
透させこれを対物重量100℃に絞りスチーマー中
に入れ、アンモニアガスを対物重量0.1%/mim
の割合で5分間室温で供給した。次にスチームを
導入し、70℃で30分間蒸熱した後、湯洗、水洗、
乾燥の順で処理し、漂白布の白度をハンター白度
計で測定した。またテンシロン(東洋ボールドウ
イン製)を使用し、10cm×10cmの正方形に切つた
綿メリヤス布が内径3cmの金属リングを通過する
際の抵抗値を風合値とした。なお漂白前の布の白
度及び風合も合わせて測定した。その結果を表1
に示す。(精練条件は、NaOH30g/、絞り率
100%、100℃×30分)
The present invention relates to a method of bleaching cellulose fibers using a novel bleaching aid in hydrogen peroxide steam bleaching. Conventional hydrogen peroxide steam bleaching of cellulose fibers involves padding a cloth with a solution containing hydrogen peroxide, sodium silicate, an alkaline agent, and a penetrating agent.
It was steam-treated at high temperatures around ℃. The pH of this pad solution is over 10, and although sodium silicate is added as a stabilizer, hydrogen peroxide gradually decomposes in the saturator, so the concentration of hydrogen peroxide cannot be maintained at a constant concentration for a long period of time or more. In reality, it is impossible to maintain the pad fluid, and the pad fluid must be replaced every day. Furthermore, the addition of sodium silicate is not at all desirable because it causes so-called silicate disorder. Furthermore, high alkali and high temperature treatments have the disadvantage of making the fibers loose and stiff, resulting in poor texture. The object of the present invention is to provide a bleaching method which overcomes the above-mentioned disadvantages. The bleaching method of the present invention uses a near-neutral method that does not contain any sodium silicate or alkaline agents.
It is characterized by applying a PH padding liquid to the fibers, treating it with ammonia gas and steaming it at 70 to 100°C. According to the bleaching method of the present invention, the pad solution is kept neutral, so the H 2 O 2 in the saturator is kept very stable. In addition, sufficient whiteness can be obtained even at a bleaching temperature of about 70°C, reducing energy costs, and in addition, products with good texture and no silicate damage can be obtained. Several studies have been conducted on neutral bleaching using H 2 O 2 . For example, Patent Publication No. 30234/1986 proposes a method using one or more substances selected from urea, dianates, sulfamic acids, and sulfamic acid salts, and condensed phosphates. Also, Patent Publication 1977-
30235 proposes a method of using a substance selected from the group consisting of phosphoric esters and phosphoric esters in combination with a substance selected from the group consisting of urea, amides, imides, dianates, sulfamic acids, and sulfamic acids. ing. However, these methods are insufficient for the activation of H 2 O 2 ;
Although it is somewhat effective for thin fabrics, when applied to bleach thick fabrics, the degree of bleaching is low and the removal of neps is incomplete. Acidic bleaching using hydrogen peroxide is also proposed in Patent Publication 1983-34674. This is a method in which an oxycarboxylic acid such as lactic acid, tartaric acid, citric acid, or glycolic acid is used in combination with hydrogen peroxide to generate an organic peracid, which is then bleached with acid. However, according to this method, removal of neps from cotton fabric is very difficult, and it would be impossible to apply it to actual bleaching. Additionally, some methods have been proposed in which so-called non-silicate stabilizers that do not contain sodium silicate are used. For example, Patent Publication No. 10425, proposed by the applicant, describes a method using a fatty acid alkali metal salt and a readily soluble magnesium salt, and Patent Publication No. 34675, which has been proposed by the applicant, discloses a method using a water-soluble protein. Methods etc. are described.
However, although the former of these methods is effective for patch bleaching, the steaming bleaching method has an insufficient bleaching effect compared to the bleaching method using sodium silicate. Furthermore, the latter poses a problem in terms of cost. However, the bleaching method of the present invention, in which a solution containing hydrogen peroxide and citrate is padded onto cloth and then steamed with ammonia gas, has a remarkable bleaching effect even at temperatures of about 70°C, and is effective even on thick cloth. It is fully applicable. Also, since it is a non-silicate bleaching method that does not contain any silicate, it has great advantages. As the easily soluble citrate, sodium salt, ammonium salt, potassium salt, etc. can be used, and the amount of citrate used is 0.05 to 1.0 based on the amount of solution.
%, preferably 0.1 to 0.3%. Adding less than 0.05% has no effect, and adding more than 0.1% does not change the effect, making it uneconomical. In this case, the addition of urea and synthetic phosphates brings good results, but the addition of oxycarboxylate salts other than citrate, such as tartrate, glycolate, malate, lactate, and glycerate, has no effect. The bleaching method of the present invention is also characterized by the use of ammonia gas before or during steaming. In this case, ammonia gas may be directly introduced into the steamer from a cylinder, or aqueous ammonia may be held at the bottom of the steamer and supplied into the steamer by evaporation. Another common alkaline agent. Caustic soda, soda carbonate, calcium hydroxide, calcium carbonate, etc. cannot be used because they are difficult to gasify. The appropriate amount of ammonia gas to be supplied is 0.1% to 20% by weight based on the weight of the fibers. If the amount of ammonia gas used is less than 0.1%, no brightening effect will be obtained, and if the amount of ammonia gas used is more than 20%, the fibrous material will become extremely brittle, which is not desirable. The ammonia gas treatment may be performed by padding the fibers with a bleaching solution, supplying ammonia gas for a certain period of time, and then steaming the fibers, or by simultaneously applying steaming to the fibers. Ammonia must be in a gaseous state during processing; for example, if aqueous ammonia is added to the padding solution, the padding solution will naturally become alkaline and H 2 O 2 will become unstable, as well as the steaming process of the padded fibers. Even if you do this, the bleaching effect is small. Next, Examples and Comparative Examples will be given to explain the present invention more specifically, but these are not intended to limit the present invention in particular. Example 1 A 40 count cotton knitted fabric scoured with an aqueous solution containing 40g/35% (weight) hydrogen peroxide solution, 2g/ sodium citrate (dihydrate), 1g/ sodium hexametaphosphate, and 2g/nonionic surfactant. Sufficiently permeate the gas, squeeze it to an objective weight of 100℃, put it in a steamer, and add ammonia gas to an objective weight of 0.1%/mim.
was fed for 5 minutes at room temperature. Next, steam is introduced and heated at 70℃ for 30 minutes, then washed with hot water and water.
The whiteness of the bleached cloth was measured using a Hunter whiteness meter. In addition, using Tensilon (manufactured by Toyo Baldwin), the resistance value when a cotton knitted cloth cut into a square of 10 cm x 10 cm passes through a metal ring with an inner diameter of 3 cm was taken as the texture value. The whiteness and texture of the cloth before bleaching were also measured. Table 1 shows the results.
Shown below. (Scouring conditions are NaOH30g/, squeezing rate
100%, 100℃ x 30 minutes)
【表】
実施例 2
35%(重量)H2O2溶液40g/、クエン酸アン
モニウム4g/、尿素5g/、非イオン界面活
性剤2g/を含む水溶液を40番手末精練綿メリヤ
ス布に充分浸透させこれを対物重量100%に絞
り、スチ―マー中でアンモニアガスを対物重量
0.07%/mim供給しながら100℃で30分間蒸熱処
理した。この後、湯洗、水洗、乾燥の順で処理
し、実施例1と同様に白度と風合を測定した。そ
の結果を表2に示す。[Table] Example 2 An aqueous solution containing 40 g of 35% (by weight) H 2 O 2 solution, 4 g of ammonium citrate, 5 g of urea, and 2 g of nonionic surfactant was sufficiently penetrated into a 40-count refined cotton knitted cloth. The ammonia gas is reduced to 100% of the objective weight in a steamer.
Steaming was performed at 100° C. for 30 minutes while supplying 0.07%/mim. Thereafter, the fabric was washed in hot water, washed in water, and dried in this order, and its whiteness and texture were measured in the same manner as in Example 1. The results are shown in Table 2.
【表】
比較例 1
実施例1と同様にして精練した40番手綿メリヤ
ス布を35%(重量)H2O2水溶液40g/、ヘキサ
メタリン酸ソーダ1g/、非イオン界面活性剤
2g/、各種オキシ酸ソーダ2g/を含む水溶
液中に入れ、充分浸透させ、これを対物重量100
%に絞り、スチーマー中に入れ、アンモニアガス
を対物重量0.1%/mimの割合で5分間室温で供
給した。次にスチームを導入し、70℃で30分間蒸
熱した後、湯洗、水洗、乾燥の順で処理し、漂白
布の白度をハンター白度計で測定した。それぞれ
のオキシ酸ソーダ別の白度を表3に示す。尚、漂
白前の布の白度は69.5である。[Table] Comparative Example 1 A 40-count cotton knitted cloth scoured in the same manner as in Example 1 was mixed with 35% (by weight) H 2 O 2 aqueous solution 40 g/, sodium hexametaphosphate 1 g/, nonionic surfactant 2 g/, and various oxidants. Put it in an aqueous solution containing 2 g of acid soda, let it penetrate thoroughly, and then add it to an objective weight of 100
%, placed in a steamer, and ammonia gas was supplied at a rate of 0.1% objective weight/mim for 5 minutes at room temperature. Next, steam was introduced and the fabric was heated at 70°C for 30 minutes, followed by washing in hot water, washing in water, and drying in that order.The whiteness of the bleached fabric was measured using a Hunter whiteness meter. Table 3 shows the whiteness of each sodium oxyacid. The whiteness of the cloth before bleaching is 69.5.
【表】
比較例 2
実施例1と同様の条件で精練した40番手綿メリ
ヤス布を下記の組成の漂白液に入れ、充分浸透さ
せ、これを対物重量100%に絞り、スチーマー中
に入れ、70℃で30分間蒸熱した後、湯洗、水洗、
乾燥の順で処理し、漂白布の白度をハンター白度
計で測定した。漂白前の白度は69.5で、漂白後の
白度は87.6であつた。[Table] Comparative Example 2 A 40-count cotton knitted fabric scoured under the same conditions as Example 1 was placed in a bleaching solution with the following composition, thoroughly penetrated, squeezed to 100% objective weight, placed in a steamer, and heated to 70% by weight. After steaming at ℃ for 30 minutes, wash with hot water, wash with water,
The whiteness of the bleached cloth was measured using a Hunter whiteness meter. The whiteness before bleaching was 69.5, and the whiteness after bleaching was 87.6.
【表】
比較例 3
H2O2(35%)40ml、クエン酸ソーダ2g/、
ヘキサメタリン酸ソーダ1g/、非イオン界面
活性剤2g/を含む水溶液にそれぞれ(イ)〜(ニ)の
量のアンモニア水(28%)を添加し、漂白液とし
た。
(イ) 0.5g/
(ロ) 1.0g/
(ハ) 5.0g/
(ニ) 20.0g/
これらのそれぞれの漂白液に実施例1と同様に
して精練した40番手綿メリヤス布を入れて液を充
分に浸透させ、これを対物重量100%に絞り、ス
チーマー中に入れて、70℃で30分間蒸熱した後、
湯洗、水洗、乾燥の順で処理し、漂白布の白度を
ハンター白度計で測定した。その結果を表4に示
す。[Table] Comparative example 3 H 2 O 2 (35%) 40ml, sodium citrate 2g/,
To an aqueous solution containing 1 g of sodium hexametaphosphate and 2 g of a nonionic surfactant, aqueous ammonia (28%) was added in amounts (a) to (d), respectively, to prepare a bleaching solution. (a) 0.5g/ (b) 1.0g/ (c) 5.0g/ (d) 20.0g/ Add 40 count cotton knitted cloth scoured in the same manner as in Example 1 to each of these bleaching solutions and pour the solution. After sufficiently permeating, squeeze this to 100% of the objective weight, put it in a steamer, and steam it at 70℃ for 30 minutes.
The bleached cloth was washed in hot water, washed with water, and dried in this order, and the whiteness of the bleached cloth was measured using a Hunter whiteness meter. The results are shown in Table 4.
Claims (1)
水素、易溶性クエン酸塩を含む水溶液を繊維にパ
ツドし、これをアンモニアガス処理及び70〜100
℃の水蒸気で蒸熱処理する繊維製品の漂白方法。1. In bleaching cellulose fiber products, the fibers are padded with an aqueous solution containing hydrogen peroxide and easily soluble citrate, treated with ammonia gas and
A method of bleaching textile products using steam treatment with steam at ℃.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55140495A JPS5766176A (en) | 1980-10-09 | 1980-10-09 | Bleaching of fiber product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55140495A JPS5766176A (en) | 1980-10-09 | 1980-10-09 | Bleaching of fiber product |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5766176A JPS5766176A (en) | 1982-04-22 |
| JPS6115182B2 true JPS6115182B2 (en) | 1986-04-23 |
Family
ID=15269947
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55140495A Granted JPS5766176A (en) | 1980-10-09 | 1980-10-09 | Bleaching of fiber product |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5766176A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3037785U (en) * | 1996-11-15 | 1997-05-20 | 株式会社ジ−・シ− | Photo holder for system notebook |
-
1980
- 1980-10-09 JP JP55140495A patent/JPS5766176A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3037785U (en) * | 1996-11-15 | 1997-05-20 | 株式会社ジ−・シ− | Photo holder for system notebook |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5766176A (en) | 1982-04-22 |
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