JP4823835B2 - Plant bleaching agent and bleaching method - Google Patents

Plant bleaching agent and bleaching method Download PDF

Info

Publication number
JP4823835B2
JP4823835B2 JP2006265355A JP2006265355A JP4823835B2 JP 4823835 B2 JP4823835 B2 JP 4823835B2 JP 2006265355 A JP2006265355 A JP 2006265355A JP 2006265355 A JP2006265355 A JP 2006265355A JP 4823835 B2 JP4823835 B2 JP 4823835B2
Authority
JP
Japan
Prior art keywords
acid
methyl
ether acetate
organic
plant
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.)
Active
Application number
JP2006265355A
Other languages
Japanese (ja)
Other versions
JP2008081463A (en
Inventor
健一 徳永
Original Assignee
株式会社佐野
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by 株式会社佐野 filed Critical 株式会社佐野
Priority to JP2006265355A priority Critical patent/JP4823835B2/en
Publication of JP2008081463A publication Critical patent/JP2008081463A/en
Application granted granted Critical
Publication of JP4823835B2 publication Critical patent/JP4823835B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

本発明は、植物の脱色剤、特に生花や葉などを使用した造花の製造において使用するのに適した脱色剤とそれを使用した脱色方法に関する。   The present invention relates to a decolorizing agent for plants, particularly a decolorizing agent suitable for use in the production of artificial flowers using fresh flowers and leaves, and a decoloring method using the same.

生花等を使用した造花の製造方法は、プリザーブドフラワーとして広く実施されており、その中では、生花等を脱色し、染色するという方法も知られている。しかし、生花等を脱色する方法は、過酸化水素系の漂白剤を使用するのがよいとされている(特許文献1の末尾、特許文献2の[0023]、特許文献3の[0007]等参照、その他、プリザーブドフラワーに関するホームページ等にも広く記載されている)が、このような従来の脱色法では、次のような問題があった。
1)脱色されない色がある(花の黄色や茎の緑等)。
2)強い酸化剤を使うため植物自体を傷めることがある。
3)脱色に時間がかかる(2日間以上を要することが多い)。
4)酸化剤が水溶性ため(アルコールの中に水が入る)植物中の水分とアルコールの置換がうまくいかない。
Artificial flower production methods using fresh flowers and the like are widely practiced as preserved flowers, and among them, a method of decoloring and dyeing fresh flowers and the like is also known. However, it is said that it is preferable to use a hydrogen peroxide-based bleach for the method of decoloring fresh flowers (Patent Document 1, [0023] Patent Document 2, [0007] Patent Document 3, etc.) However, such conventional decoloring methods have the following problems.
1) There are colors that are not decolored (flower yellow, stem green, etc.).
2) Use of a strong oxidizer may damage the plant itself.
3) Decolorization takes time (often takes 2 days or more).
4) Since the oxidizing agent is water-soluble (water enters the alcohol), the water and alcohol in the plant cannot be replaced successfully.

別途、特許文献4には、低級アルコールと有機酸からなる液を脱色液とし、これに植物体を浸漬処理する方法が開示されているが、この脱色液は、生花等を褐色化しないようにするためのものであって、24時間浸漬処理しても、生花等が白くなるまで脱色できるものではなかった。
特表平4−505766号公報 特開2004−99605号公報 特開2004−203815号公報 特開2006−111598号公報
Separately, Patent Document 4 discloses a method in which a liquid composed of a lower alcohol and an organic acid is used as a decolorizing liquid, and a plant body is immersed in the decolorizing liquid. However, this decolorizing liquid does not brown a fresh flower or the like. Therefore, even if it was immersed for 24 hours, it could not be decolored until the fresh flowers and the like became white.
JP-T-4-505766 JP 2004-99605 A JP 2004-203815 A JP 2006-111598 A

本発明は、このような欠点を解消し、過酸化水素系のような劇薬を使用することなく、生花等の植物を、耐久性よく新鮮な状態で、効率よく脱色できる脱色剤及び脱色法を提供することを課題とする。   The present invention provides a decolorizing agent and decolorizing method that can eliminate such drawbacks and efficiently decolorize plants such as fresh flowers in a durable and fresh state without using a powerful drug such as hydrogen peroxide. The issue is to provide.

本発明者は、炭素数1−3の低級アルコールと他の有機極性溶媒を組み合わせて使用し、それを酸性条件下使用することにより、前記課題を解決することを見出した。   The present inventor has found that the above problem can be solved by using a combination of a lower alcohol having 1 to 3 carbon atoms and another organic polar solvent under acidic conditions.

すなわち、本発明では、炭素数1−3の低級アルコールと他の有機極性溶媒を重量比率で50:50〜95:5の割合で含む有機溶媒に、有機酸を0.5〜10重量%の割合で添加混合してなるものを生花等の植物の脱色剤とする。   That is, in the present invention, 0.5 to 10% by weight of an organic acid is added to an organic solvent containing a lower alcohol having 1 to 3 carbon atoms and another organic polar solvent in a weight ratio of 50:50 to 95: 5. What is added and mixed at a ratio is used as a decolorizing agent for plants such as fresh flowers.

かかる本発明の脱色剤では、その中に生花等を浸漬するだけで、生花等を新鮮な状態で短時間で、効率よく白く脱色することが可能である。赤色の花では1〜2時間で完全な脱色が可能となり、従来不可能とされていた黄色の花でも、2〜5時間程度で脱色が可能となる。   With such a decolorizing agent of the present invention, it is possible to efficiently decolorize fresh flowers and the like in a short time in a short time simply by immersing the fresh flowers and the like therein. A red flower can be completely decolored in 1 to 2 hours, and a yellow flower that has been impossible in the past can be decolored in about 2 to 5 hours.

低級アルコールとしては、メタノール、エタノール、n−又はiso−プロパノールの使用が可能であるが、メタノール、エタノールの使用が好ましく、メタノールが最も効率よく使用できる。   As the lower alcohol, methanol, ethanol, n- or iso-propanol can be used, but methanol and ethanol are preferable, and methanol can be used most efficiently.

また、これら低級アルコールと組み合わせ使用する他の有機極性溶媒は、低級アルコールに可溶であり、染料溶解剤として使用可能なものであればよく、例えば、N−メチル−2−ピロリドン、NN−ジメチルアセトアミド、NN−ジメチルホルムアミド、ジメチルスルホオキサイド、エチレングリコールジメチルエーテル、ジエチレングリコールモノエチルエーテルアセテート、ジエチレングリコールモノブチルエーテルアセテート、プロピレングリコールモノメチルエーテルアセテート、エチレングリコールモノブチルエーテルアセテート、ベンジルアルコール、アセトン、メチルエチルケトン、εカプロラクタム、プロピレングリコールモノメチルエーテル、エチレングリコールモノエチルエーテル、ジエチレングリコールモノエチルエーテル、ジエチレングリコールモノブチルエーテル、エチレングリコールモノメチルエーテルアセテート、3−メトキシ−1−ブタノール、メチルイソプロピルケトン、メチルイソブチルカービノール、メチルイソブチルケトン、乳酸メチル、乳酸エチル、乳酸ブチル、ダイヤセトンアルコール、チオジグリコール、酢酸ブチル、酢酸アリル、酢酸イソプロピル、酢酸アミール、酢酸エチル、1,3−ブタンジオール及びメトキシブタノールからなる群から選ばれるものを使用するのが好ましく、これらは二種以上併用されてもよい。他の有機極性溶媒として特に好ましいのは、N−メチル−2−ピロリドン、NN−ジメチルアセトアミド、NN−ジメチルホルムアミド、ジメチルスルホオキサイド、エチレングリコールジメチルエーテル、ジエチレングリコールモノエチルエーテル、εカプロラクタム等である。これらは、単独で使用されても、混合使用されてもよく、また、添加剤を含んでも良い。また、該溶媒として、一般に染料溶解剤として市販されるものも使用可能である。例えば、LANXESS社製のLEVALIN EX-BNS、クラリアントジャパン社製のLyocol BCやLyocol KH、コタニ化学社製のソルバー580、日成化成社製のニチロンソルブN-507、日新化学社製のニッシンゾール2GやニッシンゾールCF、モーリン化学社製のモーリンTDGやモーリンゾルHIT、BASF社製のGlyecin A、Glyecin BC又はSesolvan L、大阪ケミカル社製のグリコゾールN1やグリコゾールN-150、七福化学社製のグリゾル AAC、明成化学社製のグリソルブAOX、グリソルブBE又はグリソルブZO、センカ社製のセレナゾールPDN、日華化学社製のダイセントDHやニューソルブEG、東邦化学社製のトーホーソルトA100又はCP60、ニッコー技研社製のヒドロゾールEG、ヒドロゾールN又はヒドロゾールTN、古川化学社製のペネゾールCPX、ユ二化成社製のユ二カゾールD-2、ユ二カゾールLX-7又はユ二カゾールEBなどである。   Other organic polar solvents used in combination with these lower alcohols may be those that are soluble in lower alcohols and can be used as dye solubilizers, such as N-methyl-2-pyrrolidone, NN-dimethyl. Acetamide, NN-dimethylformamide, dimethylsulfoxide, ethylene glycol dimethyl ether, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate, propylene glycol monomethyl ether acetate, ethylene glycol monobutyl ether acetate, benzyl alcohol, acetone, methyl ethyl ketone, epsilon caprolactam, propylene glycol Monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monoethyl Ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether acetate, 3-methoxy-1-butanol, methyl isopropyl ketone, methyl isobutyl carbinol, methyl isobutyl ketone, methyl lactate, ethyl lactate, butyl lactate, diacetone alcohol, thiodiglycol, It is preferable to use one selected from the group consisting of butyl acetate, allyl acetate, isopropyl acetate, amyl acetate, ethyl acetate, 1,3-butanediol and methoxybutanol, and these may be used in combination of two or more. Particularly preferred as other organic polar solvents are N-methyl-2-pyrrolidone, NN-dimethylacetamide, NN-dimethylformamide, dimethylsulfoxide, ethylene glycol dimethyl ether, diethylene glycol monoethyl ether, ε-caprolactam and the like. These may be used alone or in combination, and may contain additives. Moreover, what is generally marketed as a dye dissolving agent can also be used as this solvent. For example, LEVALIN EX-BNS manufactured by LANXESS, Lyocol BC and Lyocol KH manufactured by Clariant Japan, Solver 580 manufactured by Kotani Chemical Co., Ltd., Nichiron Solve N-507 manufactured by Nissei Kasei Co., Ltd., Nissinsol 2G manufactured by Nisshin Chemical Co., Ltd. Nissinsol CF, Morin TDG and Morinsol HIT from Morin Chemical, Glyecin A, Glyecin BC or Sesolvan L from BASF, Glycozol N1 and Glycozol N-150 from Osaka Chemical, Glysol AAC from Shichifuku Chemical Glysolve AOX, Glysolve BE or Glysolve ZO, manufactured by Meisei Chemical Co., Selenazole PDN manufactured by Senka, Dicent DH and Newsolv EG manufactured by Nikka Chemical Co., Ltd., Toho Salt A100 or CP60 manufactured by Toho Chemical Co., Ltd., manufactured by Nikko Giken Hydrozol EG, Hydrozol N or Hydrozol TN, Penezole CPX from Furukawa Chemical Co., Yunicazole D-2, Yunicazole LX-7 or Yunicazole from Yuni Kasei EB etc.

なお、低級アルコールと他の有機極性溶媒の混合割合は、重量比率で50:50〜95:5であればよいが、55:45〜90:10程度であるのが好ましい。他の有機極性溶媒の量が多すぎると、生花を新鮮状態に保ち難くなり、また、脱色の程度も悪くなる。   In addition, the mixing ratio of the lower alcohol and the other organic polar solvent may be 50:50 to 95: 5 by weight ratio, but is preferably about 55:45 to 90:10. If the amount of the other organic polar solvent is too large, it becomes difficult to keep fresh flowers fresh, and the degree of decolorization also deteriorates.

有機酸は、脱色剤を酸性に保つために添加混合されれよく、通常、脱色剤に0.5〜5重量%程度の割合で添加混合されればよく、1〜3重量%程度であるのが好ましい。   The organic acid may be added and mixed in order to keep the decoloring agent acidic. Usually, it may be added and mixed with the decoloring agent at a ratio of about 0.5 to 5% by weight, and is about 1 to 3% by weight. Is preferred.

使用される有機酸の例としては、蟻酸、酢酸、プロピオン酸、酪酸、吉草酸、イタコン酸、オクチル酸、シクロヘキサンカルボン酸、酒石酸、リンゴ酸、セバシン酸、グルコン酸、ブタンテトラカルボン酸、乳酸、レプリン酸、シュウ酸、マロン酸、マレイン酸、フマル酸、コクハク酸、グルタル酸、アジピン酸及びクエン酸などが挙げられる。   Examples of organic acids used include formic acid, acetic acid, propionic acid, butyric acid, valeric acid, itaconic acid, octylic acid, cyclohexanecarboxylic acid, tartaric acid, malic acid, sebacic acid, gluconic acid, butanetetracarboxylic acid, lactic acid, Examples include repric acid, oxalic acid, malonic acid, maleic acid, fumaric acid, succinic acid, glutaric acid, adipic acid and citric acid.

かかる本発明の脱色剤は、生花等の植物をその中に浸漬するだけで、生花等を白く脱色できるものであり、該浸漬処理は常温で実施可能である。   Such a decolorizing agent of the present invention is capable of decoloring fresh flowers and the like by simply immersing plants such as fresh flowers therein, and the immersion treatment can be carried out at room temperature.

なお、このようにして脱色した生花等は、脱色後、通常のプリザーブドフラワーの手法により種々の色に染色可能である。   In addition, the fresh flower etc. which were decolored in this way can be dye | stained to various colors by the method of a normal preserved flower after decoloring.

次に、本発明の実施例を示す。
実施例1−6及び比較例1
表1に示す組成からなる7種の脱色剤を準備し、これらの脱色剤に、常温で黄色のバラを浸漬し、脱色の状態を試験した。その結果を表1に示す。
従来、脱色できないとされていた黄色の花が、本発明に従った低級アルコールと他の有機極性媒体と有機酸を含む脱色剤では、脱色でき、特に実施例3,4では、短時間で完全に白く脱色できた。なお、有機酸として氷酢酸を使用した実施例1−3では、製品に若干酢酸臭が残ったが、イタコン酸を使用した実施例4−5では、無臭で、品質のよい製品を得ることができた。
Next, examples of the present invention will be described.
Examples 1-6 and Comparative Example 1
Seven types of decoloring agents having the compositions shown in Table 1 were prepared, and yellow roses were immersed in these decoloring agents at room temperature to test the decolorization state. The results are shown in Table 1.
Conventionally, yellow flowers, which have been considered not to be decolorized, can be decolorized with a decolorizing agent containing a lower alcohol, another organic polar medium and an organic acid according to the present invention. It was possible to decolorize white. In Example 1-3 in which glacial acetic acid was used as the organic acid, a slight acetic acid odor remained in the product, but in Example 4-5 in which itaconic acid was used, an odorless and good quality product could be obtained. did it.

Figure 0004823835
Figure 0004823835

実施例7−10及び比較例2−4
表2に示す組成からなる7種の脱色剤を準備し、これらの脱色剤に、常温で黄色のバラを浸漬し、脱色の状態を試験した。その結果を表2に示す。
本発明に従った実施例7−10では、花を新鮮な状態に保った効率のよい脱色が可能であったが、低級アルコールの使用量が少ない比較例2−4では、脱色剤への浸漬で花の状態が悪くなり、特に、比較例3−4では、脱色も悪くなった。
Example 7-10 and Comparative Example 2-4
Seven kinds of decoloring agents having the compositions shown in Table 2 were prepared, and yellow roses were immersed in these decoloring agents at room temperature to test the decolorization state. The results are shown in Table 2.
In Examples 7-10 according to the present invention, efficient decolorization was possible while keeping the flowers fresh, but in Comparative Example 2-4 where the amount of lower alcohol used was small, immersion in a decolorizing agent Thus, the state of the flowers deteriorated. In particular, in Comparative Example 3-4, decolorization also deteriorated.

Figure 0004823835
Figure 0004823835

実施例11−13
表3に示す通り、実施例10と同様の組成からなる脱色剤に赤いバラ、黄色の菊、黄色のヒマワリを浸漬し、脱色の状態を試験した。赤いバラは1時間で完全に白く脱色し、黄色の菊は黄色のバラ同様、2時間程度で脱色した。ヒマワリは水分率が少ないので少し時間がかかったが、完全脱色が可能であった。
Examples 11-13
As shown in Table 3, red roses, yellow chrysanthemums and yellow sunflowers were immersed in a decolorizing agent having the same composition as in Example 10, and the state of decolorization was tested. Red roses were completely decolorized in 1 hour, and yellow chrysanthemums were decolorized in about 2 hours, just like yellow roses. Sunflower took a little time because of its low moisture content, but it could be completely decolorized.

Figure 0004823835
Figure 0004823835

実施例14−18
表4に示す通り、組成の異なる脱色剤を種準備し、赤いバラを浸漬して、脱色の状態を試験した。実施例17,18では1−2時間で、完全に脱色し、実施例16,15,14の順に、脱色に時間がかかったが、いずれも、実用性ある脱色が可能であった。
また、黄色のバラについて浸漬試験をした結果、実施例17,18では、4−5時間で完全に脱色できた。
Examples 14-18
As shown in Table 4, five kinds of decoloring agents having different compositions were prepared, red roses were immersed, and the state of decolorization was tested. In Examples 17 and 18, the color was completely decolored in 1-2 hours, and decoloration took time in the order of Examples 16, 15, and 14. However, practical decolorization was possible in both cases.
Moreover, as a result of the immersion test on the yellow rose, in Examples 17 and 18, it was possible to completely remove the color in 4-5 hours.

Figure 0004823835
Figure 0004823835

実施例19−20
表5に示す脱色剤で、アイビーリーフと黄色のバラを脱色し、その後、染料を含む保湿剤(京華クラフト製の「一液くん」)に浸漬することにより、新鮮な状態で耐久性よく、綺麗な外観を有する製品を得ることができた、
アイビーリーフは、漂白に、花より多少多くの時間を要するが、24時間の脱色後、染色することで、綺麗に自然な色に染色された製品を得ることができ、黄色のバラは、4時間の脱色処理で完全に白く脱色され、染料入りの保湿剤への浸漬で、美しいピンクのバラに変身させることができた。
Examples 19-20
By decoloring the ivy leaf and yellow rose with the decoloring agent shown in Table 5, and then immersing in a moisturizing agent containing dye ("Kikka Craft") We were able to obtain a product with a beautiful appearance,
Ivy leaf takes a little more time than flowers to bleach, but after dyeing for 24 hours, it can be dyed to obtain a product that is beautifully dyed in natural colors. It was completely decolorized by time decoloring treatment, and it was possible to transform it into a beautiful pink rose by immersion in a moisturizer containing dye.

Figure 0004823835
Figure 0004823835

なお、アスパラペラをアイビーリーフと同様の処理をしたところ、葉を新鮮な状態に保って、自然のままの外観の製品を得ることができた。   In addition, when the asparapella was treated in the same manner as the ivy leaf, it was possible to obtain a product with a natural appearance while keeping the leaves fresh.

このようにして実施例で脱色した生花等はいずれも、通常のプリザーブドフラワーの手法で染料を加えた仕上剤を適用して所望の色に着色することができ、その結果、最初から所望の色を有する新鮮な生花であるかのような状態に仕上ることができた。   Thus, any of the fresh flowers and the like decolorized in the examples can be colored to a desired color by applying a finishing agent to which a dye is added by a conventional preserved flower method. It was possible to finish it as if it were a fresh flower.

Claims (5)

炭素数1−3の低級アルコールと、N−メチル−2−ピロリドン、NN−ジメチルアセトアミド、NN−ジメチルホルムアミド、ジメチルスルホオキサイド、ジエチレングリコールモノエチルエーテルアセテート、ジエチレングリコールモノブチルエーテルアセテート、プロピレングリコールモノメチルエーテルアセテート、エチレングリコールモノブチルエーテルアセテート、ベンジルアルコール、アセトン、メチルエチルケトン、εカプロラクタム、エチレングリコールモノメチルエーテルアセテート、メチルイソプロピルケトン、メチルイソブチルカービノール、メチルイソブチルケトン、乳酸メチル、乳酸エチル、乳酸ブチル、ダイセトンアルコール、酢酸ブチル、酢酸アリル、酢酸イソプロピル、酢酸アミール、及び酢酸エチルからなる群から選ばれる他の有機極性溶媒を、重量比率で50:50〜95:5の割合で含む有機溶媒に、有機酸を0.5〜10重量%の割合で添加混合してなることを特徴とする植物の脱色剤。 C1-C3 lower alcohol, N-methyl-2-pyrrolidone, NN-dimethylacetamide, NN-dimethylformamide, dimethylsulfoxide, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate, propylene glycol monomethyl ether acetate, ethylene glycol monobutyl ether acetate, benzyl alcohol, acetone, methyl ethyl ketone, epsilon-caprolactam, ethylene glycol monomethyl ether acetate, methylation isopropyl ketone, methyl isobutyl carbinol, methyl isobutyl ketone, methyl lactate, ethyl lactate, butyl lactate, die A seton alcohol, acetic acid butyl, allyl acetate, isopropyl acetate, Amir, and ethyl acetate Other organic polar solvent selected from Ranaru group, in a weight ratio of 50: 50-95: an organic solvent in a proportion of 5, by comprising adding and mixing an organic acid in a proportion of 0.5 to 10 wt% A plant bleaching agent characterized by. 前記他の有機極性溶媒が、N−メチル−2−ピロリドン、NN−ジメチルアセトアミド、NN−ジメチルホルムアミド、ジエチレングリコールモノブチルエーテルアセテート、メチルエチルケトンからなる群から選ばれることを特徴とする請求項1の脱色剤。 The decoloring agent according to claim 1, wherein the other organic polar solvent is selected from the group consisting of N-methyl-2-pyrrolidone, NN-dimethylacetamide, NN-dimethylformamide, diethylene glycol monobutyl ether acetate, and methyl ethyl ketone. 前記有機酸が、蟻酸、酢酸、プロピオン酸、酪酸、吉草酸、イタコン酸、乳酸、オクチル酸、シクロヘキサンカルボン酸、酒石酸、リンゴ酸、セバシン酸、グルコン酸、ブタンテトラカルボン酸、レプリン酸、シュウ酸、マロン酸、マレイン酸、フマル酸、コクハク酸、グルタル酸、アジピン酸及びクエン酸からなる群から選ばれることを特徴とする請求項1又は2の脱色剤。 The organic acid is formic acid, acetic acid, propionic acid, butyric acid, valeric acid, itaconic acid, lactic acid, octylic acid, cyclohexanecarboxylic acid, tartaric acid, malic acid, sebacic acid, gluconic acid, butanetetracarboxylic acid, repric acid, oxalic acid 3. A decolorizing agent according to claim 1 or 2, which is selected from the group consisting of malonic acid, maleic acid, fumaric acid, succinic acid, glutaric acid, adipic acid and citric acid. 前記有機酸が、酢酸、イタコン酸及び乳酸からなる群から選ばれることを特徴とする請求項1〜3のいずれかに記載の脱色剤。 The decoloring agent according to any one of claims 1 to 3, wherein the organic acid is selected from the group consisting of acetic acid, itaconic acid and lactic acid. 請求項1〜4のいずれかに記載の脱色剤に、植物を浸漬し、植物を脱色することを特徴とする植物の脱色方法。 A plant decolorization method comprising immersing a plant in the decolorizing agent according to claim 1 to decolorize the plant.
JP2006265355A 2006-09-28 2006-09-28 Plant bleaching agent and bleaching method Active JP4823835B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006265355A JP4823835B2 (en) 2006-09-28 2006-09-28 Plant bleaching agent and bleaching method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006265355A JP4823835B2 (en) 2006-09-28 2006-09-28 Plant bleaching agent and bleaching method

Publications (2)

Publication Number Publication Date
JP2008081463A JP2008081463A (en) 2008-04-10
JP4823835B2 true JP4823835B2 (en) 2011-11-24

Family

ID=39352664

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006265355A Active JP4823835B2 (en) 2006-09-28 2006-09-28 Plant bleaching agent and bleaching method

Country Status (1)

Country Link
JP (1) JP4823835B2 (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3813165B2 (en) * 2003-07-15 2006-08-23 株式会社京華クラフト Method for producing artificial flower using natural plant and finishing agent used therefor
JP4584670B2 (en) * 2004-10-18 2010-11-24 パレス化学株式会社 Fresh flower preservation method

Also Published As

Publication number Publication date
JP2008081463A (en) 2008-04-10

Similar Documents

Publication Publication Date Title
JP2003519248A (en) Eco-friendly solvent
US5049314A (en) Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate
WO2005108536A2 (en) A composition for removing a film from a substrate, a method of removing a film from a substrate, and a method of making the composition
FR2941462A1 (en) STRIPPING COMPOSITION
WO1993018865A1 (en) Aqueous stripping composition containing a peroxide and butyrolactone, ethylene carbonate or a water soluble ester
CN104139436A (en) Color fixing immersion solution applied to straw woven material dyed by perilla leaves and application method of immersion solution
NO20053452D0 (en) Aqueous dispersion of alkyd resin treated with an oxidizing agent and having improved drying properties
JP4823835B2 (en) Plant bleaching agent and bleaching method
JP4738005B2 (en) Fish skin pretreatment method
JP3813165B2 (en) Method for producing artificial flower using natural plant and finishing agent used therefor
CN110710530B (en) Compound disinfectant composition and disinfection method
US6841523B1 (en) Nail polish remover
CN109957281A (en) A kind of aqueous UV paint stripper and preparation method thereof
JPS62164612A (en) Hair dye
CN111218219A (en) Water-based resin cleaning and polishing agent
JP5277162B2 (en) Plant bleaching agent and plant bleaching method
CN109517429B (en) Deinking agent for removing ink of aluminum alloy spraying clamp jig, deinking process of aluminum alloy spraying clamp jig and aluminum alloy spraying clamp jig
JP2008057059A (en) Special processing method for preserved flower
CN101288410B (en) Scavenger for wall mould and application
JP5002514B2 (en) How to make eggplant pickles
ATE443153T1 (en) METHOD FOR PRODUCING EPTIFIBATIDE
CN113583502B (en) Medium agent and preparation method and application thereof
JP4000360B2 (en) Nickel or nickel alloy stripper on copper or copper alloy
EP3473083A1 (en) Method for marking a tree trunck with biodegradable aqueous marking paint solution and biodegradable aqueous marking paint solution
CA1320675C (en) Paint stripping composition containing five membered ring lactone

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20080625

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20110406

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20110413

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20110517

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20110720

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20110722

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20110722

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20110831

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20110907

R150 Certificate of patent or registration of utility model

Ref document number: 4823835

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140916

Year of fee payment: 3

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250