JPS59173120A - Dissolving method of tamarind seed powder - Google Patents

Dissolving method of tamarind seed powder

Info

Publication number
JPS59173120A
JPS59173120A JP4944983A JP4944983A JPS59173120A JP S59173120 A JPS59173120 A JP S59173120A JP 4944983 A JP4944983 A JP 4944983A JP 4944983 A JP4944983 A JP 4944983A JP S59173120 A JPS59173120 A JP S59173120A
Authority
JP
Japan
Prior art keywords
tamarind seed
water
seed powder
powder
paste
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
Application number
JP4944983A
Other languages
Japanese (ja)
Other versions
JPH0150448B2 (en
Inventor
Masayoshi Minami
南 昌義
Yoshizumi Hayashi
林 良純
Atsunobu Mizote
溝手 敦信
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.)
Sansho Co Ltd
Original Assignee
Sansho Co Ltd
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 Sansho Co Ltd filed Critical Sansho Co Ltd
Priority to JP4944983A priority Critical patent/JPS59173120A/en
Publication of JPS59173120A publication Critical patent/JPS59173120A/en
Publication of JPH0150448B2 publication Critical patent/JPH0150448B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To dissolve and to make tamarind seed powder pasty in water even at ordinary temp. by stirring the tamarind seed powder in water in the presence of ureas. CONSTITUTION:Tamarind seed powder is stirred in water at ordinary temp. in the presence of urea and/or thiourea. The quantity of ureas is 6pts.wt. fasing on 100pts.wt. water and >=10pts.wt. is especially preferable. As for the blending quantity of said powder, there is no limitation, and it can be selected adequately according to the desired viscosity of the pasty liquid and the uses. The pasty liquid of 5% said powder obtd. by this method, is a light brown, opaque liquid having excellent fluidity and has more superior water-holding property and viscosity than that of the pasty liquid obtd. by heating and dissolving said powder in water and very useful as thickening and water holding agents of textile printing agents and sizing liquids and binders of granular fertilizers, urea type fertilizers for foliage-scattering and seeds for vegetation.

Description

【発明の詳細な説明】 本発明はタマリンド種子粉末の溶解法に関する。さらに
詳しくは、尿素および(または)チオ尿素(以下、尿素
類という)の存在下に攪拌することを特徴とするタマリ
ンド種子粉末の溶解法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for dissolving tamarind seed powder. More specifically, the present invention relates to a method for dissolving tamarind seed powder, which is characterized by stirring in the presence of urea and/or thiourea (hereinafter referred to as ureas).

タマリンド種子粉末は、豆科植物Tamarind蝉d
iaa L−果実中の種子から外皮を除去し、粉末化す
ることによってえられる。タマリンド果実の果肉は主と
してカレー、ソースなどの食品原料として用いられ、タ
マリンド種子はその副産物としてえられるものであり、
廉価に入手できる。
Tamarind seed powder is a legume plant called Tamarind cicada.
iaa L - Obtained by removing the outer skin from the seeds in the fruit and powdering. The pulp of the tamarind fruit is mainly used as a food ingredient for curries, sauces, etc., and tamarind seeds are obtained as a by-product.
It can be obtained at a low price.

タマリンド種子粉末は粗タンパク質16.95〜20.
12%(重量%、以下同様)、粗脂肪6.06〜7.3
9%、炭水化物(多糖類)65.14〜72.17%1
粗繊維0.76〜4.62%、灰分2.45〜6.28
%からなり、灰白色ないしクリーム色の粉末であり、常
温水に分散するがその粘稠度は低い。しかしその水性分
散液を加熱すると著しく粘稠度が増大して糊化する。か
かる糊化物は古くからサイズ剤などとしてインド、パキ
スタン諸国で使用されており、最近では種々の工業分野
で分散安定剤、増粘保水剤、粘着剤、結着剤などの原料
として、その利用が図られている。
Tamarind seed powder has a crude protein of 16.95 to 20.
12% (weight%, same below), crude fat 6.06-7.3
9%, carbohydrates (polysaccharides) 65.14-72.17%1
Crude fiber 0.76-4.62%, ash 2.45-6.28
%, it is a gray-white to cream-colored powder that is dispersed in water at room temperature, but its viscosity is low. However, when the aqueous dispersion is heated, its viscosity increases significantly and gelatinizes. Such gelatinized products have been used as sizing agents in India and Pakistan since ancient times, and recently they have been used as raw materials for dispersion stabilizers, thickening water retention agents, adhesives, binders, etc. in various industrial fields. It is planned.

しかしながらタマリンド種子粉末は、前記のごとく常温
では水に分散するが溶解糊化せず、糊化するためには8
0〜950Cに加熱することが必要である。そのような
糊化のための加熱は工業的に不利であり、工業化にあた
って、常温でも水に溶解して糊化可能なタマリンド種子
粉末をうるべく、タマリンド種子粉末をエステル化、エ
ーテル化などの化学的処理により誘導体としたり、タマ
リンド種子から多糖類のみを抽出分離し精製したりして
いる。
However, as mentioned above, tamarind seed powder is dispersed in water at room temperature, but does not dissolve and gelatinize, and it takes 80% to gelatinize.
It is necessary to heat to 0-950C. Such heating for gelatinization is industrially disadvantageous, and in order to produce tamarind seed powder that can be dissolved in water and gelatinized even at room temperature, chemical processes such as esterification and etherification of tamarind seed powder are required for industrialization. Derivatives are obtained through chemical treatment, and polysaccharides are extracted and purified from tamarind seeds.

しかし、化学的処理により誘導体にするにしてもまた多
糖類を分離抽出するにしても、加工コストの増大は避け
られない。
However, regardless of whether the polysaccharide is converted into a derivative through chemical treatment or the polysaccharide is separated and extracted, an increase in processing cost is inevitable.

本発明者らは、そうしたタマリンド種子粉末自体に水溶
化処理を施さずにかつ常温でも水に溶解糊化せしめうる
タマリンド種子粉末の溶解法を開発するべく鋭意研究を
重ねた結果、タマリンド種子粉末を尿素類の存在下に水
中で攪拌するときは、常温においてもタマリンド種子粉
末が水に溶解糊化することを見出し、本発明を完成した
The present inventors have conducted intensive research to develop a method for dissolving tamarind seed powder that can be dissolved and gelatinized in water even at room temperature without subjecting the tamarind seed powder itself to water solubilization treatment. The present invention was completed based on the discovery that tamarind seed powder dissolves in water and gelatinizes even at room temperature when stirred in water in the presence of ureas.

本発明において尿素類は、タマリンド種子粉粉の水分散
液中に添加してもよいし、あらかしめ水に溶解させてお
いてもよいし、またタマリンド種子粉末とあらかじめ混
合していてもよい。
In the present invention, ureas may be added to an aqueous dispersion of tamarind seed powder, dissolved in pre-warming water, or mixed with tamarind seed powder in advance.

尿素類の量は、水100部(重量部、以下同様)に対し
て6部以上、とくに10部以上が好ましい。
The amount of urea is preferably 6 parts or more, particularly 10 parts or more, based on 100 parts (by weight, the same applies hereinafter) of water.

タマリンド種子粉末はタマリンド種子から外皮を取り除
いて粉末化したものが用いられるが、脱脂したものも用
いることができる。タマリンド種子粉末の配合鷲はとく
に制限はなく、目的とする糊液の粘度や用途に応じて適
宜選定される。
Tamarind seed powder is obtained by removing the outer skin from tamarind seeds and pulverizing them, but defatted tamarind seeds can also be used. There are no particular restrictions on the blend of tamarind seed powder, and it is appropriately selected depending on the viscosity of the intended paste and the intended use.

本発明のすぐれた効果は、タマリンド種子粉末を尿素類
の存在下に水中で攪拌するだけで常温においてタマリン
ド種子粉末を充分溶解糊化できることにあるが、所望に
より加温または加熱して溶解糊化を促進させてもよい。
The excellent effect of the present invention is that tamarind seed powder can be sufficiently dissolved and gelatinized at room temperature simply by stirring the tamarind seed powder in water in the presence of urea, but if desired, it can be dissolved and gelatinized by heating or heating. may be promoted.

攪拌に要する時間はタマリンド種子粉末の量や処理温度
、攪拌条件などによって異なるが、常温においては通常
60分間〜1時間である。
The time required for stirring varies depending on the amount of tamarind seed powder, processing temperature, stirring conditions, etc., but is usually 60 minutes to 1 hour at room temperature.

本発明の方法によってえられるたとえばタマリンド種子
粉末5%の糊液は、淡褐色の不透明できわめて流動性に
すぐれたものであり、タマリンド種子粉末を水に加熱溶
解してえられる糊液に優るも劣らない保水性、粘稠性を
示し、捺染料、サイジンダ液などの増粘保水剤1粒状肥
料の結着剤、尿素系葉面散布剤の結着剤1植生用種子結
着剤などの結着剤などとしてきわめて有用なものである
For example, a sizing solution containing 5% tamarind seed powder obtained by the method of the present invention is light brown, opaque, and extremely fluid, and is superior to a sizing solution obtained by heating and dissolving tamarind seed powder in water. It exhibits comparable water retention and viscosity, and can be used as a thickening water-retaining agent such as printing dyes and cyjinda liquid, as a binder for granular fertilizers, as a binder for urea-based foliar sprays, as a binder for seeds for vegetation, etc. It is extremely useful as an adhesive.

なお本発明の方法によってえられる糊液は、水で希釈さ
れ尿素類の濃度が下がってもタマリンド種子粉末を析出
することがない。
Note that the paste obtained by the method of the present invention does not precipitate tamarind seed powder even if it is diluted with water and the concentration of ureas is lowered.

本発明の方法によってえられる糊液は、デンプン、(1
部M(! SHP;C! 、 MO,アルギン酸ナトリ
ウム、グアーガム、ローカストビーンガム、アラビヤガ
ムなどの糊液との相溶性がよく、必要に応じそれらの他
の糊液ど併用してもよい。他の糊液と併用するときは、
タマリンド種子糊液と混合してもよいし、またタマリン
ド種子粉末の溶解時に他の糊料を共存させてもよい。い
ずれのばあいも、尿素が共存する限りにおいて他の糊料
の存在が夕w IJンド種子粉末の溶解の障害にはなら
ない。
The thickening liquid obtained by the method of the present invention contains starch, (1
Part M (! SHP; C!, MO, sodium alginate, guar gum, locust bean gum, gum arabic, etc., has good compatibility with other glues, and may be used in combination with other glues if necessary.Others When used together with glue,
It may be mixed with the tamarind seed paste liquid, or other paste materials may be present when the tamarind seed powder is dissolved. In either case, as long as urea is present, the presence of other thickeners does not impede the dissolution of the seed powder.

本発明の方法によるときは、廉価でかつ入手容易な尿素
類の存在下にタマリンド種子粉末を水に分散させるだけ
で常温においてタマリンド種子粉末を溶解糊化すること
ができ、タマリンド種子粉末の工業的価値を飛躍的に増
大せしめうる。
When using the method of the present invention, tamarind seed powder can be dissolved and gelatinized at room temperature by simply dispersing tamarind seed powder in water in the presence of inexpensive and easily available ureas, and industrial tamarind seed powder can be It can dramatically increase the value.

つぎに本発明の方法を実施例に基づいて説明するが、本
発明はかかる実施例のみに限定されるものではない。
Next, the method of the present invention will be explained based on examples, but the present invention is not limited only to these examples.

実施例1 インド産タマリンド種子粉末(200メツシュバス分9
5%以上)5部を、尿素6.0部、6.0部、9.0部
、12.0部、15.0部および1aJO部含む20°
cJの尿素水溶液95部に加えてタマリンド種子粉末の
分散液を調製した。
Example 1 Indian tamarind seed powder (200 mesh baths 9
20° containing 5 parts (5% or more), 6.0 parts, 6.0 parts, 9.0 parts, 12.0 parts, 15.0 parts of urea and 1aJO parts
A dispersion of tamarind seed powder was prepared in addition to 95 parts of cJ's urea aqueous solution.

この分散液をプロペラ攪拌機により1時間攪拌(回転数
1500rpm ) シてタマリンド種子糊液をえた゛
。それらのそれぞれの尿素濃度のばあいの粘度(BH型
粘度計、20rpm N以下同様)を調ベた。結果を第
1図に示す。
This dispersion was stirred for 1 hour using a propeller stirrer (rotation speed: 1500 rpm) to obtain a tamarind seed paste. The viscosity (BH type viscometer, 20 rpm N or less) was investigated at each of these urea concentrations. The results are shown in Figure 1.

えられたタマリンド種子糊液は尿素量の少ないものは淡
褐色の不透明の粘稠なものであったが、尿素量の増加と
ともに半透明になった。
The obtained tamarind seed paste liquid was pale brown, opaque, and viscous when the amount of urea was low, but it became translucent as the amount of urea increased.

実施例2 攪拌時間を24時間にしたほかは実施例1と同様ニシテ
翫タマリンド種子糊液をえた。それらの粘度を第1図に
示す。
Example 2 A tamarind seed paste solution was obtained in the same manner as in Example 1 except that the stirring time was changed to 24 hours. Their viscosities are shown in FIG.

実施例6 尿素に代えてチオ尿素を濃度6.0%および6.0%と
なるように加えたほかは実施例1と同様にしてタマリン
ド種子糊液をえた。それらの粘度を第1図に示す。
Example 6 A tamarind seed paste solution was obtained in the same manner as in Example 1, except that thiourea was added in place of urea at concentrations of 6.0% and 6.0%. Their viscosities are shown in FIG.

実施例4 攪拌時間を6時間にしたほかは実施例6と同様にしてタ
マリンド種子糊液をえた。それらの粘度を第1図に示す
Example 4 A tamarind seed paste solution was obtained in the same manner as in Example 6 except that the stirring time was changed to 6 hours. Their viscosities are shown in FIG.

比較例1〜2 尿素を加えなかったほかは実施例1と同様に1時間攪拌
(比較例1)および24時間攪拌(比較例2)して、比
較用のタマリンド種子糊液をえた。
Comparative Examples 1-2 Comparative tamarind seed paste liquids were obtained by stirring for 1 hour (Comparative Example 1) and stirring for 24 hours (Comparative Example 2) in the same manner as in Example 1, except that urea was not added.

実施例1と同様にして粘度を測定したところ、比較例1
の糊液では67QP、比較例2の糊液では65cpとき
わめて低い粘度であった。
When the viscosity was measured in the same manner as in Example 1, Comparative Example 1
The viscosity of the size liquid of Comparative Example 2 was 67QP, and 65 cp of the size liquid of Comparative Example 2, which was extremely low.

実施例5 実施例1で調製した種々の濃度で尿素を含むタマリンド
種子分散液をゆっくり攪拌しながら85°Cに60分間
維持してタマリンド種子糊液をえた。それらの粘度を第
1図に示す。
Example 5 The tamarind seed dispersions containing urea at various concentrations prepared in Example 1 were maintained at 85° C. for 60 minutes with slow stirring to obtain tamarind seed paste solutions. Their viscosities are shown in FIG.

第1図から明らかなように、尿素の添加量の増大にした
がって、タマリンド種子粉末がより多く溶解糊化するよ
うになる。とくに尿素およびチオ尿素濃度が6%以上の
ばあい、2oOcで溶解糊化したものと加熱溶解したも
のと同程度の粘度を示す。
As is clear from FIG. 1, as the amount of urea added increases, more tamarind seed powder is dissolved and gelatinized. In particular, when the concentration of urea and thiourea is 6% or more, the viscosity is comparable to that obtained by dissolving and gelatinizing with 2oOc and that obtained by heating.

比較例6 実施例1で用いたものと同じタマリンド種子粉末を濃度
が2%、都、6%、8%および10%となるように20
°0の水に分散し、プロペラ攪拌機により60分間攪拌
(回転数11000rp ) した。えられた比較用タ
マリンド種子糊液の粘度を第2図に示す。
Comparative Example 6 The same tamarind seed powder used in Example 1 was mixed with 20% of the tamarind seed powder at concentrations of 2%, 6%, 8% and 10%.
The mixture was dispersed in water at 0°C and stirred for 60 minutes using a propeller stirrer (rotation speed: 11,000 rpm). The viscosity of the comparative tamarind seed paste obtained is shown in FIG.

比較例4 比較例2で調製したタマリンド種子粉末の分散液を20
°Cに2時間維持して、比較用のタマリンド種子糊液を
えた。それらの粘度を第2図に示す。
Comparative Example 4 The dispersion of tamarind seed powder prepared in Comparative Example 2 was
A comparative tamarind seed paste solution was obtained by keeping at °C for 2 hours. Their viscosities are shown in FIG.

第2図から明らかなように2000の水ではタマリンド
種子粉末の溶解は進まず、加熱によって初めて溶解糊化
が生ずることがわかる。
As is clear from FIG. 2, dissolution of the tamarind seed powder does not proceed in 2000 ml of water, and dissolution and gelatinization occur only upon heating.

実施例6 実施例1で用いたものと同じタマリンド種子粉末と尿素
とを重量比で1:1に混合した混合物を、尿素の濃度が
2%、4%、6%、8%お、よ5び9%となる重量で2
0°0の水に分散させ、5種のタマリンド種子粉末の分
散液を調製した。各分散液をプロペラ攪拌機により60
分間攪拌(回転数11000rp ) l、て、タマリ
ンド種子糊液をえた。
Example 6 A mixture of the same tamarind seed powder and urea as used in Example 1 in a weight ratio of 1:1 was mixed with a urea concentration of 2%, 4%, 6%, 8%, 5%, and 5%. 2 with a weight of 9%
A dispersion of five types of tamarind seed powder was prepared by dispersing it in water at 0°0. Each dispersion was mixed with a propeller stirrer for 60 minutes.
Stir for 1 minute (rotation speed: 11,000 rpm) to obtain a tamarind seed paste solution.

それらの粘度を第1表に示す。Their viscosities are shown in Table 1.

実施例、7 実施例6で調製した5種のタマリンド種子粉末の各分散
液を80oOに1時間維持してタマリンド種子糊液をえ
た。それらの粘度を第1表に示す。
Example 7 Each dispersion of the five types of tamarind seed powder prepared in Example 6 was maintained at 80oO for 1 hour to obtain a tamarind seed paste solution. Their viscosities are shown in Table 1.

第   1   表 第1表に示すごとく、尿素が8%以上存在するときは、
20°Cの水に溶解したものと加熱溶解したものの粘度
が同じ程度になっていることがわかる。
Table 1 As shown in Table 1, when urea is present at 8% or more,
It can be seen that the viscosities of those dissolved in water at 20°C and those dissolved by heating are about the same.

実施例8 インド産タマリンド種子粉末(200メツシュパス95
%以上)100部と尿素100部を20°Cの水800
部に分散させ、プロペラ攪拌機で60分間攪拌して粘&
 150,000cPのタマリンド種子糊液をえた。
Example 8 Indian tamarind seed powder (200 methus pass 95
% or more) and 100 parts of urea in 800 parts of water at 20°C.
Stir for 60 minutes with a propeller stirrer until viscous &
A tamarind seed paste solution of 150,000 cP was obtained.

比較のためタマリンド種子粉末100部を200(!の
水900部に分散させ、前記と同様に60分間攪拌した
ところ、えられた比較用のタマリンド種子糊液の粘度は
Lloocpと低いものであった。
For comparison, 100 parts of tamarind seed powder was dispersed in 900 parts of 200 (!) water and stirred for 60 minutes in the same manner as above. The viscosity of the comparative tamarind seed paste liquid obtained was as low as Lloocp. .

この糊液を常温で一昼夜放置したところ、粘度がわずか
に1+250cPになっただけであった。
When this paste solution was left at room temperature for a day and night, the viscosity only increased to 1+250 cP.

前記尿素を含むタマリンド種子樹液を用い、つぎに示す
方法により捺染を行なった。
Printing was carried out using the tamarind seed sap containing urea by the method shown below.

(分散性染料によるポリエステル生地の捺染)カヤロン
ポリエステルブルーTS<日本化薬味部の分散性染料)
2部、クエン酸0.2部、還元防止剤(メタニトロベン
ゼンスルホン酸ナトリウム)0.1部を水67.7部に
溶解させて染料液を調製した。この染料液と前記タマリ
ンド種子糊液60部とを均一に混合し、色糊とした。
(Printing of polyester fabric with dispersible dye) Kayalon Polyester Blue TS <Dispersible dye from Nippon Kajimi Department]
A dye solution was prepared by dissolving 2 parts of citric acid, 0.2 parts of citric acid, and 0.1 part of a reduction inhibitor (sodium metanitrobenzene sulfonate) in 67.7 parts of water. This dye liquid and 60 parts of the tamarind seed paste liquid were uniformly mixed to form a colored paste.

えられた色糊を用いてぎリエステルサテン生地上にスク
リーン捺染を施し、乾燥後蒸熱処理(13000,60
分間)したのち常法により水洗した。
Using the obtained color paste, screen printing was performed on Gilliester satin fabric, and after drying, steaming treatment (13000, 60
minutes) and then washed with water in a conventional manner.

比較のため糊液としてメイプロガムNP(メイホール社
製のグアーガム加工品)の12%糊液ヲ用いて調製した
色糊により、前記と同様にポリエステルサテン生地に捺
染L タ。
For comparison, polyester satin fabric was printed in the same manner as described above using a color paste prepared using a 12% paste of Maypro Gum NP (a guar gum processed product manufactured by Mayhall Co., Ltd.) as a paste.

えられたそれぞれの捺染物のカラーパリニーは、タマリ
ンド種子糊液を用いたものの方がグアーガム加工品を用
いたものよりも高く、風合も良好であった。
The color pariny of each of the obtained prints using the tamarind seed paste liquid was higher than that using the guar gum processed product, and the texture was also better.

(塩化第一錫による地染ポリエステル生地の白色抜染)
塩化第一錫(Sn0% 2H20) 20部、ジシアン
ジアミド1部を水29部に分散させたものと前記タマリ
ンド種子糊液50部とを均一に混合し、抜染糊を調製し
た。
(White discharge printing of ground-dyed polyester fabric using stannous chloride)
A dispersion paste was prepared by uniformly mixing 50 parts of the tamarind seed paste solution with 20 parts of stannous chloride (Sn0% 2H20) and 1 part of dicyandiamide dispersed in 29 parts of water.

比較のためハスバインディTG −10(敷島紡績■製
のヒドロキシプロピルエーテル化された冷水可溶のタマ
リンド種子粉末)の12%$211液を用いたほかは前
記と同様にして比較用の抜染糊を調製した。
For comparison, a discharge printing paste for comparison was prepared in the same manner as described above, except that a 12% $211 solution of Hasbindi TG-10 (hydroxypropyl etherified cold water soluble tamarind seed powder manufactured by Shikishima Boseki) was used. Prepared.

えら−れた各抜染糊を用い、ミケトンポリエステルデイ
スチャージプルーRの5%染液で地染されたポリエステ
ル平織生地に印捺し、乾燥後170°Cで8分間連続高
温蒸熱機で蒸熱処理したのち、常法により水洗、乾燥し
たところ、タマリンド種子糊液を用いたものの抜染部分
の白色度はきわめて満足のいくものであり、かつ風合い
も良好であった。一方、タマリンド種子加工品を用いた
比較用の抜染糊のば゛あいは抜染部分がやや黄褐色を呈
していた。
Using each of the selected discharge printing pastes, printing was carried out on a polyester plain weave fabric that had been ground-dyed with a 5% dye solution of Miketon Polyester Discharge Plue R. After drying, it was steam-treated at 170°C for 8 minutes in a continuous high-temperature steamer. Afterwards, when washed with water and dried in a conventional manner, the whiteness of the discharge-printed area using tamarind seed paste liquid was extremely satisfactory, and the texture was also good. On the other hand, in the case of the comparative discharge printing paste using processed tamarind seeds, the discharged areas were slightly yellowish brown.

(アルカリ抜染) 炭酸カリウム6部、炭酸ナトリウム6部、ポリエチレン
グリフール8部およびグリセリン8部を前記タマリンド
種子糊液50部に混合し、さらに水を加えて100部の
アルカリ抜染糊を調製した。相溶性は良好で糊液の分離
あるいはゲル化はみられず、抜染糊は流動性に富むもの
であった。
(Alkali discharge printing) 6 parts of potassium carbonate, 6 parts of sodium carbonate, 8 parts of polyethylene glycol, and 8 parts of glycerin were mixed with 50 parts of the tamarind seed paste solution, and water was further added to prepare 100 parts of an alkaline discharge paste. The compatibility was good, no separation or gelation of the paste solution was observed, and the discharge printing paste was highly fluid.

このアルカリ抜染糊を用いて5%のダイアエックスレッ
ドA2B −FSペースト(三菱化成工業■製)と0.
2%ケルテックスp(ケルコ社製飄アルギン酸ナトリウ
ム)を含む染液にパディングし、乾燥しでえたポリエス
テルジコーゼツ1mに印捺し、乾燥棟180°Oで6分
間連続高温蒸熱機で熱処理したのち、常法により水洗し
た。抜染部分の白色度ならびに絵柄のシャープ性は良好
であった。
Using this alkaline discharge dyeing paste, 5% Diax Red A2B-FS paste (manufactured by Mitsubishi Chemical Industries, Ltd.) and 0.
Padded with a dye solution containing 2% Keltex P (sodium alginate manufactured by Kelco), printed on 1 m of dried polyester jikozetsu, heat treated in a continuous high temperature steamer for 6 minutes at 180°O in a drying building, It was washed with water using a conventional method. The whiteness of the discharge printed area and the sharpness of the pattern were good.

実施例9 インド産脱脂タマリンド種子粉末(200メツシュパス
95%以上)80部とチオ尿素50部とを870部の2
0°C水に分散させプロペラ攪拌機で60分間攪拌し、
120*000cPのタマリンド種子糊液をえた。なお
チオ尿素を含まない脱脂タマリンド種子粉末の8%分散
液の粘度は450 cPであった。
Example 9 870 parts of 80 parts of Indian defatted tamarind seed powder (200 mesh pass 95% or more) and 50 parts of thiourea
Disperse in 0°C water and stir for 60 minutes with a propeller stirrer.
A tamarind seed paste solution of 120*000cP was obtained. The viscosity of an 8% dispersion of defatted tamarind seed powder containing no thiourea was 450 cP.

前記チオ尿素を含む脱脂タマリンド種子糊液を用いてポ
リアクリル生地の捺染を行なった◇カチ四ンオレンジR
H(商品名、保土谷化学工業株製のカチオン染料)5部
を2部のチオジエチレングリコールと10部の水とで混
練しペースト状とし、さらにリンゴ酸1部、還元防止剤
(メタニトロベンゼンスルホン酸ナトリウム)0.1部
を加えさらに水を追加し、合計40部の染料溶液を調製
した。この染料溶液と60部のチオ尿素を含む脱脂タマ
リンド種子糊液とを均一に混合して色糊をえた。この色
糊の粘度は9,800cPであった。
Polyacrylic fabric was printed using the defatted tamarind seed paste containing thiourea ◇Kachishin Orange R
Knead 5 parts of H (trade name, cationic dye manufactured by Hodogaya Chemical Industry Co., Ltd.) with 2 parts of thiodiethylene glycol and 10 parts of water to form a paste, and then add 1 part of malic acid and a reduction inhibitor (metanitrobenzenesulfonic acid). 0.1 part of sodium) was added and water was further added to prepare a total of 40 parts of a dye solution. This dye solution and a defatted tamarind seed paste solution containing 60 parts of thiourea were uniformly mixed to obtain a colored paste. The viscosity of this colored paste was 9,800 cP.

この色糊を用いてアクリルモスリン生地上に印捺乾燥し
たのち、100°Oで60分間蒸熱した。
This colored paste was printed and dried on an acrylic muslin fabric, and then steamed at 100°O for 60 minutes.

その後、常法により水洗して仕上げた。生地の風合いは
良好であり、均染性も良好であった。
Thereafter, it was finished by washing with water using a conventional method. The texture of the fabric was good, and the level dyeing property was also good.

実施例10 実施例8で用いたものと同じタマリンド種子粉末10部
を常温の水80部に分散させたものの中に尿素6部、チ
オ尿素4部を加え、60分間攪拌したところ、分散して
いたタマリンド種子粉末が膨潤溶解し、糊液となった。
Example 10 10 parts of the same tamarind seed powder used in Example 8 was dispersed in 80 parts of water at room temperature, and 6 parts of urea and 4 parts of thiourea were added and stirred for 60 minutes. The tamarind seed powder swelled and dissolved to form a paste.

この糊液の粘度は160*000aPであった。The viscosity of this glue was 160*000 aP.

この糊液を用いてナイ四ン編物生地の捺染を行なった。This paste was used to print a four-dimensional knitted fabric.

すなわち、スミノールファーストオレンジpo(商品名
、住友化学工業■製の酸性染料)2部、チオジエチレン
グリコール1部、熱水5部を加えて染料粉末をよく溶解
したのちクエン酸0.5部を加え、さらに水を追加して
40部の染料溶液とした。これに前記糊液40部とソル
ビトーゼO−S (商品名、アベベ社製、オランダ)の
12%糊液20部とを混入し、色糊としたO糊料の相溶
性は良好であり、ゲル化あるいは分離などは生じていな
かった。
That is, 2 parts of Suminol Fast Orange po (trade name, acid dye manufactured by Sumitomo Chemical Co., Ltd.), 1 part of thiodiethylene glycol, and 5 parts of hot water were added to dissolve the dye powder well, and then 0.5 part of citric acid was added. , more water was added to make 40 parts of the dye solution. This was mixed with 40 parts of the above size liquid and 20 parts of 12% size liquid of Sorbitose O-S (trade name, manufactured by Abebe, Netherlands) to form a colored paste. No separation or separation occurred.

この色糊を用いてナイ四ンジャージイ生地にスクリーン
捺染を行なったところ、スクリーンからの透過性、浸透
性は良好であった。乾燥後100°Oで蒸熱し、水洗し
て仕上げた。生地の風合い、カラーバリユー、均染性、
浸透性などすべて良好であった。
When screen printing was performed on a jersey fabric using this color paste, the permeability and permeability through the screen were good. After drying, it was steamed at 100°O and washed with water. Fabric texture, color value, level dyeing,
Everything was good including permeability.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は実施例1〜6および比較例1γ2でそれぞれえ
られたタマリンド種子糊液の粘度と尿素濃度との関係を
示すグラフ、第2図は比較例3〜4でそれぞれえられた
タマリンド種子糊液の粘度とタマリンド種子粉末濃度と
の関係を示すグラフである。
Figure 1 is a graph showing the relationship between the viscosity and urea concentration of tamarind seed paste liquids obtained in Examples 1 to 6 and Comparative Example 1γ2, and Figure 2 is a graph showing the relationship between tamarind seeds obtained in Comparative Examples 3 to 4, respectively. It is a graph showing the relationship between the viscosity of paste liquid and the concentration of tamarind seed powder.

Claims (1)

【特許請求の範囲】 1 タマリンド種子粉末を尿素および(または)チオ尿
素の存在下に水中で攪拌することを特徴とするタマリン
ド種子粉末の溶解法。 2 常温で行なう特許請求の範囲第1項記載の方法。
[Claims] 1. A method for dissolving tamarind seed powder, which comprises stirring tamarind seed powder in water in the presence of urea and/or thiourea. 2. The method according to claim 1, which is carried out at room temperature.
JP4944983A 1983-03-23 1983-03-23 Dissolving method of tamarind seed powder Granted JPS59173120A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4944983A JPS59173120A (en) 1983-03-23 1983-03-23 Dissolving method of tamarind seed powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4944983A JPS59173120A (en) 1983-03-23 1983-03-23 Dissolving method of tamarind seed powder

Publications (2)

Publication Number Publication Date
JPS59173120A true JPS59173120A (en) 1984-10-01
JPH0150448B2 JPH0150448B2 (en) 1989-10-30

Family

ID=12831444

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4944983A Granted JPS59173120A (en) 1983-03-23 1983-03-23 Dissolving method of tamarind seed powder

Country Status (1)

Country Link
JP (1) JPS59173120A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006198496A (en) * 2005-01-19 2006-08-03 Miyoshi Oil & Fat Co Ltd Solid waste treatment method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006198496A (en) * 2005-01-19 2006-08-03 Miyoshi Oil & Fat Co Ltd Solid waste treatment method
JP4535888B2 (en) * 2005-01-19 2010-09-01 ミヨシ油脂株式会社 Solid waste disposal method

Also Published As

Publication number Publication date
JPH0150448B2 (en) 1989-10-30

Similar Documents

Publication Publication Date Title
DK167243B1 (en) PROCEDURE FOR INTRODUCING DIVALENT IONS IN SOLVENT ALGINATE SOLUTIONS FOR PREPARING A MIXTURE AND PRINT COLOR, ANIMAL FOOD AND FOOD CONTAINING THE MIXTURE
US4753659A (en) Derivatives of cassia tora polysaccarides and their use
CN100532704C (en) Thickener for textile printing paste
EP0025679A2 (en) Multicolor coating system, process for producing it, process using it to achieve a multicolor pattern on a surface, and articles having such multicolor patterns
JPS6099082A (en) Calcium alginate/sodium alginate printing
JPS59173120A (en) Dissolving method of tamarind seed powder
US4426206A (en) Textile printing paste composition with highly substituted carboxymethyl cellulose
DE3347469A1 (en) Substituted alkyl ethers of Cassia polysaccharides, and the use thereof as thickeners
CN106592266B (en) A kind of anti-impression method of polyamide -ester plus material hot melt
JPH0623355B2 (en) Adhesive composition for corrugated board
JPS59230073A (en) Hydroxyalkyl-carboxymethylated tamarind gum
US5417754A (en) Composition and method for selective removal of fabric design image
JP3219922B2 (en) Carboxymethylcellulose and its use in textile printing
US5415790A (en) Thickening agent for treating textile material
JPS628553B2 (en)
JPH10292272A (en) Printing paste, printing, resist printing paste and resist printing
JPS6385186A (en) Dyeing of cellulosic fiber cloth
JPH0518951B2 (en)
JPS5940952B2 (en) printing paste
EP0044601B1 (en) Process for discharge printing of polyester materials
El-Thalouth et al. Effect of Enzymatic Treatment of Starch Gelatinized with Urea
JPS605710B2 (en) Printing paste
JPS58220881A (en) Printing size
JP2914751B2 (en) Stabilization of aqueous compositions containing anionic surfactants
JPH0291282A (en) Size for printing