Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP3892925B2 - Manufacturing method of artificially contaminated cloth - Google Patents
[go: Go Back, main page]

JP3892925B2 - Manufacturing method of artificially contaminated cloth - Google Patents

Manufacturing method of artificially contaminated cloth Download PDF

Info

Publication number
JP3892925B2
JP3892925B2 JP01458697A JP1458697A JP3892925B2 JP 3892925 B2 JP3892925 B2 JP 3892925B2 JP 01458697 A JP01458697 A JP 01458697A JP 1458697 A JP1458697 A JP 1458697A JP 3892925 B2 JP3892925 B2 JP 3892925B2
Authority
JP
Japan
Prior art keywords
cloth
artificially contaminated
soil
organic solvent
contaminated cloth
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 - Fee Related
Application number
JP01458697A
Other languages
Japanese (ja)
Other versions
JPH10204769A (en
Inventor
浩司 笹田
将嗣 山元
勲 山田
正仁 千脇
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP01458697A priority Critical patent/JP3892925B2/en
Publication of JPH10204769A publication Critical patent/JPH10204769A/en
Application granted granted Critical
Publication of JP3892925B2 publication Critical patent/JP3892925B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Landscapes

  • Treatment Of Fiber Materials (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は、人工汚染布の製造方法に関する。さらに詳しくは、衣料用洗剤の開発、評価、洗浄研究などの際に用いられる人工汚染布の製造方法に関する。
【0002】
【従来の技術】
人工汚染布は、衣料用洗剤の開発、評価、洗浄研究などを行なう際には必要不可欠なものである。
【0003】
従来、人工汚染布としては、種々の汚れを付着させたものが数多く開発されており、かかる人工汚染布に使用される溶媒には、例えば、テトラクロロエチレン(パークレン)、四塩化炭素などの塩素系有機溶剤が使用されている。
【0004】
しかしながら、これらの塩素系有機溶剤は、人体に対して有害であり、また廃水汚染や大気汚染を引き起こすおそれがある。
【0005】
したがって、前記塩素系有機溶剤を必要としない人工汚染布の開発が待ち望まれている。
【0006】
【発明が解決しようとする課題】
本発明は、前記従来技術に鑑みてなされたものであり、人体などに対する安全性に優れ、さらに乾燥効率が高く、製造時の時間を短縮化させることができる人工汚染布の製造方法を提供することを目的とする。
【0007】
【課題を解決するための手段】
本発明は、沸点が90℃以下であり、引火点を有しないフッ素原子含有有機溶媒に汚れ成分を分散または溶解させてなり、汚れ成分を1〜70重量%含有する汚れ液を、試験布に付着させることを特徴とする人工汚染布の製造方法に関する。
【0008】
【発明の実施の形態】
本発明の製造方法によれば、沸点が90℃以下であり、引火点を有しないフッ素原子含有有機溶媒に汚れ成分を分散または溶解させて得られた汚れ液を、試験布に付着させることにより、人工汚染布を得ることができる。
【0009】
以下に、本発明の人工汚染布の製造方法を図面に基づいて説明する。
【0010】
図1は、本発明の人工汚染布の製造方法の一実施態様を示す概略説明図であるが、本発明はかかる態様のみに限定されるものではない。
【0011】
図1において、布送り出しローラー1 には、試験布2が巻回されている。
【0012】
布送り出しローラー1には、例えば、重り式などの試験布2の走行速度を制御するためのブレーキ装置が装着されていてもよい。
【0013】
試験布2は、汚れ試験に供されるものであればよく、例えば、衣料などに用いられる布地などがあげられる。前記布地としては、例えば、木綿などの天然繊維、ポリエステル繊維、ナイロン繊維、アクリル繊維などの合成繊維などがあげられる。
【0014】
試験布2は、支持棒3上を走行したのち、例えば一定速度で、汚れ液4が注がれた汚染浴5中に浸漬される。
【0015】
前記汚れ液4は、前記したように、沸点が90℃以下であり、引火点を有しないフッ素原子含有有機溶媒に、汚れ成分を分散または溶解させたものである。
【0016】
本発明においては、有機溶剤として、沸点が90℃以下であり、引火点を有しないフッ素原子含有有機溶媒が用いられている点に、1つの大きな特徴がある。
【0017】
本発明においては、前記フッ素原子含有有機溶媒の沸点が90℃以下であることから、揮発性に優れ、厚手の生地を用いた場合であっても該フッ素原子含有有機溶媒をほぼ完全に乾燥させることができるので、作業性が向上するという利点がある。また、前記フッ素原子含有有機溶媒は、引火点を有しないことから、火災や爆発などに対する安全性に優れ、塩素系有機溶媒と対比して、人体に及ぼす影響が非常に小さいという優れた性質が発現される。
【0018】
前記沸点が90℃以下であり、引火点を有しないフッ素原子含有有機溶媒の代表例としては、例えば、1,1−ジクロロ−2,2,3,3,3−ペンタフルオロプロパン、1,3−ジクロロ−1,1,2,2,3−ペンタフルオロプロパンなどがあげられ、これらは単独でまたは2種以上を混合して用いることができる。これらのフッ素原子を有する化合物は、人体に対する安全性に優れ、乾燥性に優れ、また得られる人工汚染布に残存しがたいので、本発明においては好適に使用しうるものである。
【0019】
また、前記汚れ成分としては、例えば、固体粒子汚れなどがあげられる。かかる固体粒子汚れの代表例としては、例えば、鹿沼赤玉土の粉砕物などの無機質汚れの粉末物質であることが実際に家庭での汚れを想定した場合に適切である。
【0020】
前記引火点を有しないフッ素原子含有有機溶媒に、前記汚れ成分を添加し、分散または溶解させることにより、汚れ液4が得られる。このとき、汚れ成分を均一に試験布2に付着させ、また洗浄効果を容易に確認することができるようにするために、前記汚れ成分の汚れ液4中における濃度は、かかる汚れ成分の種類にもよるが、通常、1〜70重量%程度であることが好ましい。
【0021】
前記汚染浴5中の汚れ液4は、例えば、回転ブラシ6や空気攪拌装置(図示せず)などにより、攪拌させることができる。
【0022】
汚れ液4中に浸漬された試験布2は、つぎに、回転ブラシ6と接触させ、摺擦させることにより、その両面が汚れ液4に含まれている汚れ成分によって汚染される。前記回転ブラシ6としては、例えば、獣毛などの天然毛、樹脂製の人造毛のブラシや、縮絨させた毛織物などがあげられる。
【0023】
次に、汚染された試験布2は、絞りローラー7へ導かれる。この絞りローラー7によって汚染された試験布2に含まれた汚れ液4が絞られ、汚れ成分が試験布2に定着される。このとき、試験布2の走行速度は、均一に汚れを付着させるという点から、一定にすることが好ましい。
【0024】
汚れ成分の定着後、試験布2は、乾燥室8に導入される。図1に示されている乾燥室8は、熱風乾燥室であるが、本発明は、かかる乾燥室8の種類によって限定されるものではない。乾燥室8の下方には、熱風吹き出し口9が設けられている。かかる熱風吹き出し口9から放出される熱風は、例えば、送風機から搬送された空気を加熱器内に送入し、電熱器などで加熱することによって生じさせることができる。このようにして放出された熱風によって試験布2が乾燥される。
【0025】
次に、乾燥された試験布2は、汚れ落とし室10に導入される。この汚れ落とし室10で、試験布2は、回転ブラシ11と接触し、該試験布2に付着している過剰の汚れ成分が落とされる。かかる回転ブラシ11は、前記回転ブラシ6と同じものであってもよい。
【0026】
付着していた過剰の汚れ成分を試験布2から落として得られた人工汚染布は、例えば、引っ張りローラー12で牽引され、必要により、汚染布巻取りローラー13で巻き取られる。
【0027】
前記したように、本発明においては、試験布2に汚れ液4を付着させ、例えば、回転ブラシ6などにより、汚れ成分を試験布2に付着させた後、乾燥させ、過剰に付着した汚れ成分を、例えば回転ブラシ11などで除去するという操作を採用した場合には、現実に即した人工汚染布を容易に製造することができるという利点がある。
【0028】
かくして、本発明の製造方法によって得られた人工汚染布は、従来法と対比して、乾燥効率が高く、また溶媒の残留がほとんどないという優れた性質を有するものである。
【0029】
さらに、本発明の製造方法によれば、人工汚染布を製造する際の乾燥効率が高いことから、靴下、トレーナー、肌着などに用いられている実用着衣により近い厚手の生地を用いた場合であっても、フッ素原子含有有機溶媒を残留させずに、ほぼ完全に該フッ素原子含有有機溶媒を乾燥させることができるという利点がある。
【0030】
【実施例】
次に、本発明を実施例に基づいてさらに詳細に説明するが、本発明はかかる実施例のみに限定されるものではない。
【0031】
実施例1
図1に示されるような人工汚染布の製造装置を用いた。
【0032】
汚れ液4として、1,1−ジクロロ−2,2,3,3,3−ペンタフルオロプロパン(沸点:51.1℃)45重量%および1,3−ジクロロ−1,1,2,2,3−ペンタフルオロプロパン(沸点:65.1℃)55重量%からなる有機溶媒(沸点:54℃)に固体粒子汚れとして鹿沼赤玉土を添加し、固体粒子汚れの濃度が12.0g/lである汚れ液を用いた。
【0033】
試験布2として、木綿金巾2003布(木綿平織または木綿メリヤス)を用い、これを1.3 m/分の走行速度で前記汚れ液(液温:20℃)4中に浸漬し、回転ブラシ6と接触させ、摺擦させることにより、その両面が汚れ液4に含まれている汚れ成分によって汚染させた。
【0034】
次に、汚染された試験布2を絞りローラー7へ導き、この絞りローラー7によって汚染された試験布2に含まれた汚れ液4を絞り取った。
【0035】
汚れ成分の定着後、試験布2を、熱風乾燥室(80℃)8に導入し、乾燥時間を木綿平織で1.7分間、また木綿メリヤスで1.5分間として乾燥させた。
【0036】
次に、乾燥させた試験布2を、汚れ落とし室10に導入し、この汚れ落とし室10で、試験布2を回転ブラシ11と接触させ、試験布2に付着している過剰の汚れ成分を落とした。
【0037】
かくして得られた人工汚染布を引っ張りローラー12で牽引し、汚染布巻取りローラー13で巻き取った。
【0038】
次に、得られた人工汚染布の反射率を測色色差計(日本電色工業(株)製、ND−300A、測定波長:460nm)で測定したところ、46±1%であった。
【0039】
次に、得られた人工汚染布の特性を以下の方法にしたがって調べた。その結果を表1に示す。
【0040】
(1)溶媒残留量
試験布(木綿平織)を6cm×6cmの大きさに裁断し、このサンプル5 枚を各有機溶媒中に浸漬したのち、ローラーで絞り、有機溶媒の付着量を0.11gに調整した。次に、室温で15時間放置し、有機溶媒の残留量を式:
〔有機溶媒の残留量〕
=〔人工汚染布の重量−試験布の重量−汚れ成分の付着重量〕
÷〔試験布の重量〕
にしたがって求めた。
【0041】
なお、汚れ成分の付着量は、式:
〔汚れ成分の付着量〕
=〔人工汚染布の重量−試験布の重量〕÷〔試験布の重量〕
にしたがって求めた。
【0042】
(2)洗浄力
4°DH(ドイツ硬度)または8°DH(ドイツ硬度)を有する20℃の硬水1000mlに、JISB洗剤1.0gを溶解させて洗剤液を得た。
【0043】
この洗剤液20℃中に人工汚染布を8cm×8cmの大きさで5枚浸漬し、ターゴトメーター((株)上島製作所製)を用いて100rpmの回転速度で、10分間洗浄し、流水すすぎを30秒間行なった。
【0044】
次に、洗浄率を式:
〔洗浄率(%)〕
=〔洗浄後の人工汚染布の反射率−洗浄前の人工汚染布の反射率〕
÷〔試験布の反射率−洗浄前の人工汚染布の反射率〕
×100
にしたがって求めた。
【0045】
比較例1〜2
実施例1において、溶媒としてテトラクロロエチレン(沸点:121℃)(比較例1)またはイソプレン系グリコールエーテル(クラレ(株)製、商品名:ファイントップJ−410)80重量%と水20重量%とからなる水溶液(沸点:100〜170℃)(比較例2)を用い、走行速度を1.3m/分(比較例1)または0.8m/分(比較例2)とし、また乾燥時間を比較例1で木綿平織について1.7分間、木綿メリヤスについて2分間とし、比較例2で木綿平織について2.9分間、木綿メリヤスについて4.6分間としたほかは実施例1と同様にして人工汚染布を得た。
【0046】
得られた人工汚染布の特性を実施例1と同様にして調べた。その結果を表1に示す。
【0047】
【表1】

Figure 0003892925
【0048】
表1に示された結果から、実施例1で得られた人工汚染布は、比較例1〜2におけるように、従来の塩素系有機溶剤が用いられた人工汚染布と対比して、有機溶媒の残留量が少ないことがわかる。また、実施例1の方法によれば、洗浄時間が短くても、比較例1〜2の方法と同等の洗浄効果が発現されるので、乾燥効率が高いことがわかる。
【0049】
【発明の効果】
本発明の製造方法によれば、塩素系有機溶剤を必要しないので、人体などに対する安全性に優れ、また乾燥効率が高く、製造時の時間を短縮化させて人工汚染布を製造することができるという優れた効果が奏される。
【図面の簡単な説明】
【図1】図1は、本発明の人工汚染布の製造方法の一実施態様を示す概略説明図である。
【符号の説明】
1 布送り出しローラー
2 試験布
3 支持棒
4 汚れ液
5 汚染浴
6 回転ブラシ
7 絞りローラー
8 乾燥室
9 熱風吹き出し口
10汚れ落とし室
11回転ブラシ
12引っ張りローラー
13汚染布巻取りローラー[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for manufacturing an artificially contaminated cloth. More specifically, the present invention relates to a method for producing an artificially contaminated cloth used in the development, evaluation, and cleaning research of a laundry detergent.
[0002]
[Prior art]
Artificial contaminated cloth is indispensable when developing, evaluating and cleaning research on detergents for clothing.
[0003]
Conventionally, many artificially contaminated cloths with various stains have been developed. Solvents used for such artificially contaminated cloths include, for example, chlorinated organic materials such as tetrachloroethylene (parklene) and carbon tetrachloride. Solvent is used.
[0004]
However, these chlorinated organic solvents are harmful to the human body and may cause wastewater pollution and air pollution.
[0005]
Therefore, development of an artificially contaminated cloth that does not require the chlorinated organic solvent is awaited.
[0006]
[Problems to be solved by the invention]
The present invention has been made in view of the prior art, and provides a method for manufacturing an artificially contaminated cloth that is excellent in safety to human bodies and the like, has high drying efficiency, and can shorten the time for manufacturing. For the purpose.
[0007]
[Means for Solving the Problems]
In the present invention, a soil solution having a boiling point of 90 ° C. or less and having a soil component dispersed or dissolved in a fluorine atom-containing organic solvent having no flash point and containing 1 to 70% by weight of the soil component is applied to a test cloth. The present invention relates to a method for manufacturing an artificially contaminated cloth characterized by being adhered.
[0008]
DETAILED DESCRIPTION OF THE INVENTION
According to the production method of the present invention, a soil solution obtained by dispersing or dissolving a soil component in a fluorine atom-containing organic solvent having a boiling point of 90 ° C. or less and having no flash point is attached to a test cloth. , You can get an artificially contaminated cloth.
[0009]
Below, the manufacturing method of the artificial contamination cloth of this invention is demonstrated based on drawing.
[0010]
FIG. 1 is a schematic explanatory view showing one embodiment of the method for producing an artificially contaminated cloth of the present invention, but the present invention is not limited to such an embodiment.
[0011]
In FIG. 1, a test cloth 2 is wound around a cloth feed roller 1.
[0012]
For example, a brake device for controlling the traveling speed of the test cloth 2 such as a weight type may be attached to the cloth feed roller 1.
[0013]
The test cloth 2 only needs to be subjected to a soil test, and examples thereof include cloth used for clothing and the like. Examples of the fabric include natural fibers such as cotton, synthetic fibers such as polyester fibers, nylon fibers, and acrylic fibers.
[0014]
After running on the support rod 3, the test cloth 2 is immersed, for example, in a contaminated bath 5 in which the soil liquid 4 is poured at a constant speed.
[0015]
As described above, the soil liquid 4 is obtained by dispersing or dissolving a soil component in a fluorine atom-containing organic solvent having a boiling point of 90 ° C. or less and having no flash point.
[0016]
The present invention has one major feature in that a fluorine atom-containing organic solvent having a boiling point of 90 ° C. or less and having no flash point is used as the organic solvent.
[0017]
In the present invention, since the boiling point of the fluorine atom-containing organic solvent is 90 ° C. or less, the fluorine atom-containing organic solvent is almost completely dried even when a thick dough is used. Therefore, there is an advantage that workability is improved. In addition, since the fluorine-containing organic solvent has no flash point, it is excellent in safety against fires and explosions, and has an excellent property of having a very small effect on the human body as compared with a chlorinated organic solvent. Expressed.
[0018]
Representative examples of the fluorine-containing organic solvent having a boiling point of 90 ° C. or less and having no flash point include, for example, 1,1-dichloro-2,2,3,3,3-pentafluoropropane, 1,3 -Dichloro-1,1,2,2,3-pentafluoropropane and the like can be mentioned, and these can be used alone or in admixture of two or more. These compounds having a fluorine atom are excellent in safety to the human body, excellent in drying properties, and hardly remain in the resulting artificially contaminated cloth, and therefore can be suitably used in the present invention.
[0019]
Examples of the soil component include solid particle soil. As a representative example of such solid particle soil, for example, a powder material of inorganic soil such as crushed material of Kanuma Akadama is appropriate when soil at home is actually assumed.
[0020]
The stain solution 4 is obtained by adding and dispersing or dissolving the stain component in the fluorine atom-containing organic solvent having no flash point. At this time, in order to allow the dirt component to uniformly adhere to the test cloth 2 and to make it possible to easily confirm the cleaning effect, the concentration of the dirt component in the dirt liquid 4 depends on the type of the dirt component. However, it is usually preferably about 1 to 70% by weight.
[0021]
The dirt liquid 4 in the contamination bath 5 can be stirred by, for example, a rotating brush 6 or an air stirring device (not shown).
[0022]
The test cloth 2 immersed in the dirt liquid 4 is then brought into contact with the rotating brush 6 and rubbed with the test cloth 2 to be contaminated with dirt components contained in the dirt liquid 4. Examples of the rotating brush 6 include natural hairs such as animal hair, artificial hair brushes made of resin, and knitted woolen fabrics.
[0023]
Next, the contaminated test cloth 2 is guided to the squeeze roller 7. The dirt liquid 4 contained in the contaminated test cloth 2 is squeezed by the squeezing roller 7, and the dirt component is fixed on the test cloth 2. At this time, it is preferable that the running speed of the test cloth 2 is constant from the viewpoint that dirt is uniformly attached.
[0024]
After fixing the soil component, the test cloth 2 is introduced into the drying chamber 8. The drying chamber 8 shown in FIG. 1 is a hot air drying chamber, but the present invention is not limited by the type of the drying chamber 8. A hot air outlet 9 is provided below the drying chamber 8. The hot air discharged from the hot air outlet 9 can be generated by, for example, sending air conveyed from a blower into a heater and heating it with an electric heater or the like. The test cloth 2 is dried by the hot air thus discharged.
[0025]
Next, the dried test cloth 2 is introduced into the dirt removing chamber 10. In this dirt removal chamber 10, the test cloth 2 comes into contact with the rotating brush 11, and excess dirt components adhering to the test cloth 2 are removed. The rotating brush 11 may be the same as the rotating brush 6.
[0026]
The artificially contaminated cloth obtained by removing the excessive soil component adhering to the test cloth 2 is pulled by, for example, the pulling roller 12 and wound by the contaminated cloth winding roller 13 as necessary.
[0027]
As described above, in the present invention, the dirt liquid 4 is adhered to the test cloth 2 and, for example, the dirt component is adhered to the test cloth 2 by the rotating brush 6 or the like, and then dried, and the dirt component adhered excessively. In the case of adopting an operation of removing, for example, the rotating brush 11 or the like, there is an advantage that an artificially contaminated cloth that is realistic can be easily manufactured.
[0028]
Thus, the artificially contaminated cloth obtained by the production method of the present invention has excellent properties such as high drying efficiency and almost no residual solvent, as compared with the conventional method.
[0029]
Furthermore, according to the production method of the present invention, since the drying efficiency when producing artificially contaminated cloth is high, it is a case where a thick fabric closer to the practical clothes used for socks, trainers, underwear, etc. is used. However, there is an advantage that the fluorine atom-containing organic solvent can be dried almost completely without leaving the fluorine atom-containing organic solvent.
[0030]
【Example】
Next, the present invention will be described in more detail based on examples, but the present invention is not limited to such examples.
[0031]
Example 1
An artificially contaminated cloth manufacturing apparatus as shown in FIG. 1 was used.
[0032]
As the stain liquid 4, 1,1-dichloro-2,2,3,3,3-pentafluoropropane (boiling point: 51.1 ° C.) 45% by weight and 1,3-dichloro-1,1,2,2, Kanuma Akadama is added as solid particle soil to an organic solvent (boiling point: 54 ° C.) consisting of 55% by weight of 3-pentafluoropropane (boiling point: 65.1 ° C.), and the solid particle soil concentration is 12.0 g / l. A certain soil solution was used.
[0033]
As the test cloth 2, a cotton gold cloth 2003 (cotton plain weave or cotton knitted fabric) was used, immersed in the soil solution (liquid temperature: 20 ° C.) 4 at a running speed of 1.3 m / min, and contacted with the rotating brush 6. The both surfaces were contaminated with the dirt component contained in the dirt liquid 4 by rubbing and rubbing.
[0034]
Next, the contaminated test cloth 2 was guided to the squeezing roller 7, and the soil solution 4 contained in the test cloth 2 contaminated by the squeezing roller 7 was squeezed out.
[0035]
After fixing the soil components, the test cloth 2 was introduced into a hot air drying room (80 ° C.) 8 and dried for 1.7 minutes with a plain cotton weave and 1.5 minutes with a cotton knitted fabric.
[0036]
Next, the dried test cloth 2 is introduced into the dirt removing chamber 10. In this dirt removing chamber 10, the test cloth 2 is brought into contact with the rotating brush 11, and excess dirt components adhering to the test cloth 2 are removed. Dropped.
[0037]
The artificially contaminated cloth thus obtained was pulled by the pulling roller 12 and wound by the contaminated cloth winding roller 13.
[0038]
Next, when the reflectance of the obtained artificially contaminated cloth was measured with a colorimetric color difference meter (Nippon Denshoku Industries Co., Ltd., ND-300A, measurement wavelength: 460 nm), it was 46 ± 1%.
[0039]
Next, the characteristics of the obtained artificially contaminated cloth were examined according to the following method. The results are shown in Table 1.
[0040]
(1) Residual amount of solvent Test cloth (cotton plain weave) is cut into a size of 6 cm x 6 cm, and after immersing 5 samples in each organic solvent, the amount of organic solvent adhered is 0.11 g Adjusted. Next, it is allowed to stand at room temperature for 15 hours, and the residual amount of the organic solvent is expressed by the formula:
[Residual amount of organic solvent]
= [Weight of artificially contaminated cloth-Weight of test cloth-Weight of dirt components]
÷ [Weight of test cloth]
It was calculated according to
[0041]
In addition, the amount of adhesion of dirt components is the formula:
[Amount of dirt components]
= [Weight of artificially contaminated cloth-Weight of test cloth] ÷ [Weight of test cloth]
It was calculated according to
[0042]
(2) A detergent solution was obtained by dissolving 1.0 g of JISB detergent in 1000 ml of 20 ° C. hard water having a cleaning power of 4 ° DH (German hardness) or 8 ° DH (German hardness).
[0043]
5 pieces of artificially contaminated cloth with a size of 8 cm × 8 cm are immersed in this detergent solution at 20 ° C., washed with a targotometer (manufactured by Ueshima Seisakusho Co., Ltd.) at a rotation speed of 100 rpm for 10 minutes, and rinsed with running water. For 30 seconds.
[0044]
Next, the cleaning rate is expressed by the formula:
[Washing rate (%)]
= [Reflectance of artificially contaminated cloth after washing-Reflectance of artificially contaminated cloth before washing]
÷ [Reflectance of test cloth-reflectance of artificially contaminated cloth before washing]
× 100
It was calculated according to
[0045]
Comparative Examples 1-2
In Example 1, as a solvent, tetrachloroethylene (boiling point: 121 ° C.) (Comparative Example 1) or isoprene-based glycol ether (manufactured by Kuraray Co., Ltd., trade name: Fine Top J-410) 80% by weight and 20% by weight of water An aqueous solution (boiling point: 100-170 ° C.) (Comparative Example 2) is used, the running speed is 1.3 m / min (Comparative Example 1) or 0.8 m / min (Comparative Example 2), and the drying time is Comparative Example. 1 for 1.7 minutes for cotton plain weave, 2 minutes for cotton knitted fabric, 2.9 minutes for plain cotton weave in Comparative Example 2 and 4.6 minutes for cotton knitted fabric, artificially contaminated cloth as in Example 1. Got.
[0046]
The characteristics of the obtained artificially contaminated cloth were examined in the same manner as in Example 1. The results are shown in Table 1.
[0047]
[Table 1]
Figure 0003892925
[0048]
From the results shown in Table 1, the artificially contaminated cloth obtained in Example 1 was compared with the artificially contaminated cloth using the conventional chlorinated organic solvent as in Comparative Examples 1 and 2, and the organic solvent. It can be seen that the residual amount of is small. Moreover, according to the method of Example 1, even if cleaning time is short, since the cleaning effect equivalent to the method of Comparative Examples 1-2 is expressed, it turns out that drying efficiency is high.
[0049]
【The invention's effect】
According to the production method of the present invention, since a chlorinated organic solvent is not required, it is excellent in safety for human bodies and the like, has high drying efficiency, and can produce an artificially contaminated cloth by shortening the production time. An excellent effect is achieved.
[Brief description of the drawings]
FIG. 1 is a schematic explanatory view showing an embodiment of a method for producing an artificially contaminated cloth according to the present invention.
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 1 Cloth feed roller 2 Test cloth 3 Support stick 4 Dirt liquid 5 Contamination bath 6 Rotating brush 7 Drawing roller 8 Drying chamber 9 Hot air outlet 10 Dirt removing chamber 11 Rotating brush 12 Pulling roller 13 Contaminated cloth winding roller

Claims (4)

沸点が90℃以下であり、引火点を有しないフッ素原子含有有機溶媒に汚れ成分を分散または溶解させてなり、汚れ成分を1〜70重量%含有する汚れ液を、試験布に付着させることを特徴とする人工汚染布の製造方法。A soil component is dispersed or dissolved in a fluorine atom-containing organic solvent having a boiling point of 90 ° C. or less and has no flash point, and a soil solution containing 1 to 70% by weight of the soil component is adhered to the test cloth. A method for producing an artificially contaminated cloth. 汚れ液を試験布に付着させた後、乾燥させ、過剰に付着した汚れ成分を除去する請求項1記載の人工汚染布の製造方法。The method for producing an artificially contaminated cloth according to claim 1, wherein the stain liquid is attached to the test cloth and then dried to remove excessively attached dirt components. フッ素原子含有有機溶媒が1,1−ジクロロ−2,2,3,3,3−ペンタフルオロプロパンおよび1,3−ジクロロ−1,1,2,2,3−ペンタフルオロプロパンよりなる群から選ばれた少なくとも1種である請求項1または2記載の人工汚染布の製造方法。The fluorine atom-containing organic solvent is selected from the group consisting of 1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,3-dichloro-1,1,2,2,3-pentafluoropropane The method for producing an artificially contaminated cloth according to claim 1 or 2, wherein the artificially contaminated cloth is at least one kind. 汚れ成分が固体粒子汚れである請求項1〜3いずれか記載の人工汚染布の製造方法。The method for producing an artificial soiled cloth according to any one of claims 1 to 3, wherein the soil component is solid particle soil.
JP01458697A 1997-01-10 1997-01-10 Manufacturing method of artificially contaminated cloth Expired - Fee Related JP3892925B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP01458697A JP3892925B2 (en) 1997-01-10 1997-01-10 Manufacturing method of artificially contaminated cloth

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP01458697A JP3892925B2 (en) 1997-01-10 1997-01-10 Manufacturing method of artificially contaminated cloth

Publications (2)

Publication Number Publication Date
JPH10204769A JPH10204769A (en) 1998-08-04
JP3892925B2 true JP3892925B2 (en) 2007-03-14

Family

ID=11865280

Family Applications (1)

Application Number Title Priority Date Filing Date
JP01458697A Expired - Fee Related JP3892925B2 (en) 1997-01-10 1997-01-10 Manufacturing method of artificially contaminated cloth

Country Status (1)

Country Link
JP (1) JP3892925B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105820795B (en) * 2015-01-07 2018-12-21 南京绿泽宇和精细化工有限公司 The production method that spot is used in experiment

Also Published As

Publication number Publication date
JPH10204769A (en) 1998-08-04

Similar Documents

Publication Publication Date Title
JP5881619B2 (en) Improved washing machine and washing method
US3442692A (en) Method of conditioning fabrics
CN102713043B (en) The cleaning equipment improved
JP2012517876A (en) Cleaning device
AU2001266721B2 (en) Home laundry method
US20120048299A1 (en) Novel cleaning method
AU2001266721A1 (en) Home laundry method
MXPA03000608A (en) Textile cleaning processes and apparatuses.
JPS5831172A (en) Fiber treating agent
Novotna et al. Release of microplastic fibers from polyester knit fleece during abrasion, washing, and drying
JP2019081993A (en) Damage process for textile products
JP3892925B2 (en) Manufacturing method of artificially contaminated cloth
DE102007029485B4 (en) Process for cleaning in particular sensitive cleaning goods
JP2000328455A (en) Fiber treatment agent
JPS6159461B2 (en)
JPS59112069A (en) Product for treating garment
JP2005034410A (en) Laundry auxiliary cloth
JPH02104770A (en) Treating agent for synthetic fiber
TWI521115B (en) Improved cleaning apparatus and method
CN112368442A (en) Method for conditioning textiles and conditioned textiles produced therefrom
JPWO2021014620A1 (en) Manufacturing method of shrink-proof animal hair fiber
JP2001107090A (en) Detergent for cleaning and cleaning method using the same
JPH07268766A (en) Anti-shrink agent for washing with water and method for washing dry products by washing with water
CN113853460A (en) Polyester fiber structure, method for producing same, clothing, and bedding
JPH04316665A (en) Cleaning

Legal Events

Date Code Title Description
A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20050707

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20050818

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20051006

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: 20061204

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20061208

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

Free format text: PAYMENT UNTIL: 20091215

Year of fee payment: 3

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

Free format text: PAYMENT UNTIL: 20101215

Year of fee payment: 4

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

Free format text: PAYMENT UNTIL: 20101215

Year of fee payment: 4

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

Free format text: PAYMENT UNTIL: 20111215

Year of fee payment: 5

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

Free format text: PAYMENT UNTIL: 20111215

Year of fee payment: 5

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

Free format text: PAYMENT UNTIL: 20121215

Year of fee payment: 6

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

Free format text: PAYMENT UNTIL: 20121215

Year of fee payment: 6

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

Free format text: PAYMENT UNTIL: 20131215

Year of fee payment: 7

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees