JPS5930879A - Frothing molded product - Google Patents

Frothing molded product

Info

Publication number
JPS5930879A
JPS5930879A JP13930082A JP13930082A JPS5930879A JP S5930879 A JPS5930879 A JP S5930879A JP 13930082 A JP13930082 A JP 13930082A JP 13930082 A JP13930082 A JP 13930082A JP S5930879 A JPS5930879 A JP S5930879A
Authority
JP
Japan
Prior art keywords
acid
weight
parts
100pts
alkali metal
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
JP13930082A
Other languages
Japanese (ja)
Other versions
JPS6019946B2 (en
Inventor
Masanori Oota
正典 太田
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical 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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP13930082A priority Critical patent/JPS6019946B2/en
Publication of JPS5930879A publication Critical patent/JPS5930879A/en
Publication of JPS6019946B2 publication Critical patent/JPS6019946B2/en
Expired legal-status Critical Current

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  • Cosmetics (AREA)
  • Oxygen, Ozone, And Oxides In General (AREA)
  • Detergent Compositions (AREA)

Abstract

PURPOSE:To obtain titled product free from any degradation even during a long storage period, providing excellent frothing performance when charged in water, to effect complete dissolution, by incorporating boron oxide in a granular formulation comprising a hydrogen peroxide adduct and others followed by press molding. CONSTITUTION:The objective product can be obtained by first incorporating (A) 100pts.wt. of a granular formulation comprising (i) 100pts.wt. of a hydrogen peroxide adduct, and (ii) 4-500pts.wt. of a chlorinated isocyanuric acid or peroxysulfuric acid (hydrogen) salt, or (iii) 100pts.wt. of an alkali metal (bi)carbonate and (iv) 10-100pts.wt. of a solid (in)organic acid with (B) 0.1-3pts.wt. of boron oxide, followed by carrying out a press molding under a pressure, normally, of 50-600kg/cm<2>. USE:Cleaning agents for medical, industrial, and domestic use; for example, a cleaning agent for articicial teeth.

Description

【発明の詳細な説明】 本発明は、保存中に変質が生起しない安定な起泡性成形
物の改良に係わる。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to the improvement of stable foamable molded products that do not undergo deterioration during storage.

従来よp、水中に投入した際気泡′を発生する錠剤が、
医薬、工業用及び家庭用洗浄剤、入れ歯の洗浄剤等各種
の分野で実用されている。これら起泡剤としては、過酸
化水素付加物に塩素化インシアタール酸。パーオキシ硫
酸塩、バー芽キシ硫酸水素塩等を配合し加圧成形したも
の。
Conventionally, tablets that generate bubbles when placed in water,
It is used in various fields such as medicine, industrial and household cleaning agents, and denture cleaning agents. These foaming agents include hydrogen peroxide adducts and chlorinated intheater acid. Pressure-molded product containing peroxysulfate, barium hydrogensulfate, etc.

或は、アルカリ金属炭酸塩、アルカリ金属重炭酸塩等に
固体の有機酸若しくは無機酸を配合し成形したもの等が
一般に知られているが、いずれも吸湿性を示すために1
通常の包装容器1例えば、ポリエチレン製の袋に密封保
存するときけ、徐々に吸湿と分解が起こシ、甚々しき場
合には1分解発生ガスによって袋が破損することも起こ
っている。また、完全に吸湿を抑えるべく、防湿包装に
て保存しても、原料中の及び)JIJ工時の微量の水分
によυ同様な問題が生起している。
Alternatively, products made by blending solid organic or inorganic acids with alkali metal carbonates, alkali metal bicarbonates, etc. are generally known, but in order to exhibit hygroscopicity,
When an ordinary packaging container 1 is stored sealed in a polyethylene bag, for example, it gradually absorbs moisture and decomposes, and in severe cases, the bag may be damaged by the gas generated by the decomposition. Furthermore, even if the product is stored in moisture-proof packaging to completely suppress moisture absorption, similar problems occur due to trace amounts of moisture in the raw materials and during JIJ processing.

しかし、か\る問題点の解消を意図した提案も幾つか見
られるが、未だ充分なものが得られていない。例えば、
タノシ゛り、ゼオライト、シリカ等の粉末を添加するこ
とにより吸湿性を抑制する方法では、起泡剤中を水中に
投入した際。
However, although there have been some proposals intended to solve these problems, nothing has yet been achieved. for example,
In the method of suppressing hygroscopicity by adding powders such as tanoshi, zeolite, and silica, when the foaming agent is added to water.

水が濁υ、また。別の例として、起泡剤成分の過酸化水
素付加化合物1重炭酸塩等の表面をボリビニルアルコー
ルでコーティングする方法も知られているが、か\る処
理を施した成分からなる起泡剤を水中に投入すると、充
分な起泡効果が得らhないことが多い。更に別の例とし
ては、起泡剤成分を積層溝造となるように成形した錠剤
も知られているが、が\る錠剤の製造は容易でないのみ
ならず、やは逆水中に投入した際の起泡効果も尚充分で
はない。
The water is cloudy, again. As another example, a method is known in which the surface of a foaming agent component such as hydrogen peroxide addition compound monobicarbonate is coated with polyvinyl alcohol; When added to water, a sufficient foaming effect is often not obtained. Another example is a tablet in which a foaming agent component is molded into a laminated groove structure. The foaming effect is still not sufficient.

本発明者らは研究の結果、過炭酸す) IJウム。As a result of our research, the present inventors found that hypercarbonate (IJum).

過硼酸ナトリウム等とジクロロイソシアヌール酸す) 
IJウムの粉状配合物に更に酸化硼素B2O5全〃[1
えて加圧成形した成形物を0通常のポリエチレン製袋に
密封下保存すると、極めて長期間分解ガスの発生が起ら
ず、しかも水中に投入したv′Aにも極めて良好な起泡
性を示し、成形物の成分は完全に溶解し、水が濁らない
ことを見出し本発明を完成した。
Sodium perborate, etc. and dichloroisocyanuric acid)
Boron oxide B2O5 total [1
When the molded product is sealed and stored in an ordinary polyethylene bag, no decomposition gas is generated for an extremely long period of time, and it shows extremely good foaming properties even when placed in water. They completed the present invention by discovering that the components of the molded product were completely dissolved and the water did not become cloudy.

本発明の目的は。長期間の保存中に変質が起らず、水中
に投入した際にも極めて良好な起泡性を示し、水に完全
に溶解する起泡性成形物を提供することにある。本発明
の安定な起泡性成形物は、過酸化水素伺加化合物100
重夙部と塩素化イソシアヌール酸、パーオキシ硫酸塩若
しくはパーオキシ硫酸水素塩4〜500重量部を含む粉
状配合物又はアルカリ金属炭酸塩若しくはアルカリ金属
重炭酸塩100重計部と固体の有機酸若しくは無機酸1
0〜100重量部を含む粉状配合物の100重量部に酸
化硼素を01〜50重量部を加え加圧成形したことを特
徴とする。
The purpose of the present invention is to: The object of the present invention is to provide a foamable molded product that does not undergo deterioration during long-term storage, exhibits extremely good foaming properties even when placed in water, and is completely soluble in water. The stable foamable molded product of the present invention contains hydrogen peroxide compound 100%
A powder formulation containing 4 to 500 parts by weight of chlorinated isocyanuric acid, peroxysulfate or peroxyhydrogensulfate, or 100 parts by weight of alkali metal carbonate or alkali metal bicarbonate and a solid organic acid or Inorganic acid 1
It is characterized in that 01 to 50 parts by weight of boron oxide is added to 100 parts by weight of a powdery compound containing 0 to 100 parts by weight, and the mixture is press-molded.

本発明に用いられろ過酸化水素付加化合物としては1例
えば、過炭酸ナトリウム、過硼酸ナトリウム、過りん酸
ナトリウム等が挙げられる。
Examples of the filtered hydrogen oxide addition compound used in the present invention include sodium percarbonate, sodium perborate, and sodium perphosphate.

本発明に用いられる塩素化インシアヌール酸としてハ、
トリクロロインシアヌール酸、ジクUロインシアヌール
酸、ジクロロイソシアヌール酸のナトリウム若しぐはカ
リウムの無水塩又は含水塩性が挙げられる。好ましい塩
素化イソシアヌール酸は、ジクロロインシアヌール酸カ
リウム、ジクロロイソシアヌール酸す)・リウムの無水
塩、ジクロロイソシアヌール酸ナトリウムの2水塩等で
ある。本発明に用いられるパーオキシ硫酸塩又はパーオ
キシ硫酸水素塩としては。
As the chlorinated incyanuric acid used in the present invention, c.
Examples include anhydrous sodium or potassium salts or hydrated salts of trichloroin cyanuric acid, dichloroin cyanuric acid, and dichloroisocyanuric acid. Preferred chlorinated isocyanuric acids include potassium dichloroisocyanurate, anhydrous salt of lium dichloroisocyanurate, and sodium dichloroisocyanurate dihydrate. The peroxysulfate or peroxyhydrogensulfate used in the present invention includes:

例えば、パーオキシ硫酸ナトリウム、パーオキシ硫酸カ
リウム、パーオキシ硫酸水素ナトリウム、パーオキシ硫
酸水素カリウム等が挙げられる。本発明に用いられるア
ルカリ金属炭酸塩若しくはアルカリ金属重炭酸塩として
は9例えば。
Examples include sodium peroxysulfate, potassium peroxysulfate, sodium peroxyhydrogensulfate, potassium peroxyhydrogensulfate, and the like. Examples of the alkali metal carbonate or alkali metal bicarbonate used in the present invention include 9.

炭酸ナトリウム、炭酸カリウム、炭酸水素ナトリウノ2
.炭酸水素カリウム等が挙げられる。また1本発明に用
いられる固体の有機酸若しくは無機酸の例としては、く
えん酸、酒石酸、アジピン酸、りんご酸、こはく酸、硼
酸、スルファミン酸、酸性リン酸塩等が挙げられる。こ
れら過酸化水素付加化合物、塩素化イソシアタール酸。
Sodium carbonate, potassium carbonate, sodium bicarbonate Uno 2
.. Examples include potassium hydrogen carbonate. Examples of the solid organic or inorganic acids used in the present invention include citric acid, tartaric acid, adipic acid, malic acid, succinic acid, boric acid, sulfamic acid, and acidic phosphates. These hydrogen peroxide adducts, chlorinated isotheateric acid.

パーオキシ硫酸塩、パーオキシ硫酸水素塩。Peroxysulfate, peroxyhydrogensulfate.

アルカリ金属炭酸塩、アルカリ金属重炭酸塩。Alkali metal carbonates, alkali metal bicarbonates.

固体の有機酸、固体の無機酸等は、いずれも市販工業製
品として入手できるが、特に含水率が約3%以下つ粉状
品が好ましい。
Solid organic acids, solid inorganic acids, etc. are all available as commercially available industrial products, but powdered products with a moisture content of about 3% or less are particularly preferred.

上記過酸化水素付加化合物に対し、上記塩素化イソシア
ヌール酸。パーオキシ硫酸塩、パーオキシ硫酸水素塩等
は、水中で酸化剤として作用し9分解による酸素ガスめ
発生を起こさせる作用をする。また、上記アルカリ金属
炭酸塩若しくはアルカリ金属重炭酸塩に対し、上記固体
の有機酸、無機酸等は、水中で中和反応により。
In contrast to the above hydrogen peroxide addition compound, the above chlorinated isocyanuric acid. Peroxy sulfates, peroxy hydrogen sulfates, etc. act as oxidizing agents in water and cause the generation of oxygen gas through decomposition. In addition, the solid organic acid, inorganic acid, etc. for the alkali metal carbonate or alkali metal bicarbonate are neutralized in water.

炭酸ガスを発生させる作用をする。上記過酸化水素付加
化合物と塩素化イソシアタール酸。パーオキシ硫酸塩、
パーオキシ硫酸水素塩等との配合物、或いは、上記アル
カリ金属炭酸塩、アルカリ金属爪炭酸塩等と固体の有機
酸、無機酸等との配合物は、粉状のま\では保存中に変
質しやす<、iた使用時の粉立ち、計量のトラブルもあ
り、特に水中での分散が乏しいので通常。
It acts to generate carbon dioxide gas. The above hydrogen peroxide addition compound and chlorinated isotheateric acid. peroxysulfate,
Blends with peroxy hydrogen sulfate, etc., or blends of the above-mentioned alkali metal carbonates, alkali metal nail carbonates, etc. with solid organic acids, inorganic acids, etc., do not deteriorate during storage if they are in powder form. There are also problems with powder dust and measuring problems when using it, especially since it has poor dispersion in water.

これら配合物は更に加圧成形した粒剤、丸剤又は錠剤と
して用いらtしる。しかし、これら加圧成形した起泡剤
でも前記の如く保存中に吸湿を起こし、その除徐々に分
解ガスを発生し、長期間の保存後には、かなりの変質ど
なって所期の起泡効果が得られない。
These formulations may also be used as pressed granules, pills or tablets. However, even these pressure-molded foaming agents absorb moisture during storage as described above, and as the moisture is removed, decomposition gas is generated.After long-term storage, the properties deteriorate considerably and the desired foaming effect is not achieved. is not obtained.

本発明の起泡剤は、上記加圧成形前に、上記粉状の起泡
性配合物に更に酸化硼素B、03を添加し、加圧成形す
ることにより得られた錠剤、丸剤又は粒剤である。本発
明に用いられる酸化硼素は、起泡剤中で強力な吸湿)生
を示すが、これによって捕捉さicた水分は遊離水とし
て存在せずに、酸化硼素を硼酸に変換せしめる作用をし
The foaming agent of the present invention is a tablet, pill or granule obtained by further adding boron oxide B, 03 to the powdery foaming composition before the pressure molding. It is a drug. The boron oxide used in the present invention exhibits strong hygroscopicity in the foaming agent, and thus the trapped moisture acts to convert the boron oxide into boric acid without existing as free water.

生成した硼酸は起泡剤の水中溶解性及び起泡性に何らの
影響も与えず、起泡剤の変質を防いで。
The produced boric acid has no effect on the foaming agent's solubility in water and foaming properties, and prevents the foaming agent from deteriorating in quality.

これを安定に保存せしめる作用をする。加圧成形された
好ましい起泡剤を得るVCは、その配合成分の性状及び
組成に限定が必要であることが見1に3さitた。過酸
化水素付7Jl+化合物100重量部に、塩素化インシ
アタール酸。パーオキシ硫酸塩、パーオキシ硫酸水素塩
等を4重量部以下又は500重景重量上配合した粉状配
合物に酸化硼素を加えて加圧成形した起泡剤、或いは。
It acts to preserve it stably. It has been found that in order to obtain a preferable pressure-molded foaming agent, it is necessary to limit the properties and composition of the blended components. 7 Jl with hydrogen peroxide + 100 parts by weight of the compound, chlorinated intheater acid. A foaming agent prepared by adding boron oxide to a powdered mixture containing peroxysulfate, peroxyhydrogensulfate, etc. in an amount of 4 parts by weight or less or 500 parts by weight or more, and then press-molding the mixture.

アルカリ金属炭酸塩、アルカリ金属重炭酸塩の100重
量部に固体の有機酸、無機酸等を10重量部以下又は1
00重量部以上配上記た粉状で、配合物の分散、溶解が
不均一となり好ましくない。また、加えるべき酸化硼素
の量が、上記粉状配合物100重量部に対し01重量部
以下では、前記変質防止効果に乏しくなり、−1,た。
100 parts by weight of alkali metal carbonate or alkali metal bicarbonate and 10 parts by weight or less of solid organic acid, inorganic acid, etc. or 1 part by weight or less.
00 parts by weight or more is not preferable because the dispersion and dissolution of the compound will be uneven. Furthermore, if the amount of boron oxide to be added is less than 0.1 parts by weight per 100 parts by weight of the powdery compound, the deterioration prevention effect becomes poor, and -1.

50重世部以上では、起泡剤中の起泡有効成分の濃度が
低下し、やはり充分な起泡性が付与できない。上記組成
にわいて、塩素化イソどアヌール酸を使用するときは、
特にその過狙IJルが含有されるとき水中において殺菌
、漂白等の効果も併せ示し、特に好寸しい場合もある。
If the amount exceeds 50 parts, the concentration of the foaming active ingredient in the foaming agent decreases, and sufficient foaming properties cannot be imparted. Regarding the above composition, when using chlorinated isodoanuric acid,
In particular, when the overly targeted IJ is contained, it also exhibits sterilizing, bleaching, and other effects in water, and may be particularly advantageous.

本発明の起泡剤としては1本発明の目的が達成ざiする
限り、上記配合成分の他に更に任意の成分1例えば5着
色剤、香料、界面活性剤、増量剤等を配合したものも差
支えない。通常1着色剤、香料1等は少量の添加で充分
であるが。
As long as the purpose of the present invention is achieved, the foaming agent of the present invention may contain, in addition to the above-mentioned ingredients, optional ingredients such as colorants, fragrances, surfactants, fillers, etc. No problem. Usually, it is sufficient to add a small amount of coloring agent 1, fragrance 1, etc.

洗浄効果を付与させろ場合、必要に応じて界面活性剤金
増υ口させてもよい。また増量剤は、水溶性、非変質性
、起泡性を損なわない成分を適量選んで使用する必要が
ある。上記粉状配合物及びこれに更に酸化硼素を加えた
配合物は、その配合成分が均−VC混合されていること
が好ましく1通常1粒度60〜3000μ程度の粉状の
配合成分及び酸化硼素を、v型プレンダー等上記の如く
、過酸化水素伺加化合物100重量部と塩素化イソシア
ヌール酸、パーオキシ硫酸塩若しくはパーオキシ硫酸水
素塩4〜500重量部を含む粉状配合物又はアルカリ金
属炭酸塩若しくはアルカリ金属重炭酸塩100重量部と
固体の有機酸若しくは無機酸1o〜100重量部を含む
粉状配合物の100M量部Vr−酸化硼素を01〜30
重量部を加えて均一混合物となし。
If a cleaning effect is to be imparted, surfactant gold may be added as necessary. In addition, as the extender, it is necessary to select an appropriate amount of components that are water-soluble, non-altering, and do not impair foaming properties. It is preferable that the above-mentioned powdery compound and a compound in which boron oxide is added are evenly mixed with VC. , v-type blender, etc. As mentioned above, a powdery formulation containing 100 parts by weight of a hydrogen peroxide compound and 4 to 500 parts by weight of a chlorinated isocyanuric acid, peroxysulfate or peroxyhydrogensulfate, or an alkali metal carbonate or 100 M parts of a powdered formulation containing 100 parts by weight of an alkali metal bicarbonate and 10 to 100 parts by weight of a solid organic or inorganic acid Vr - 01 to 30 parts by weight of boron oxide
Add parts by weight to make a homogeneous mixture.

こiしを更に加圧成形することにより得られる。It is obtained by further pressure molding the strained material.

加圧成形の方法としては9通常の乾式または湿式の造粒
法が採用できる。f!I、tば、乾式法としては打錠機
、ブリケッティングマシノ、コンパクテイングマシン等
が挙げられる。成形圧力け100 l(g/cnl以下
1通常50〜600 Kg/crjが用いられる。か\
る圧力で成形することにより。
As a method of pressure molding, a conventional dry or wet granulation method can be adopted. f! Examples of the dry method include a tablet press, a briquetting machine, and a compacting machine. Molding pressure 100 l (g/cnl or less 1 Usually 50 to 600 Kg/crj is used.
By molding under pressure.

密度1,4〜1,9程度の成形物が得られろ。不発いて
得られるフレーク状2粒子状等でよい。錠剤の場合は1
箇当りの重さについても特に制限はないが1通常05〜
200f程度でよい。
A molded product with a density of about 1.4 to 1.9 can be obtained. It may be in the form of flakes or two particles obtained by misfire. 1 for tablets
There is no particular restriction on the weight per piece, but it is usually 05~
Approximately 200f is sufficient.

かぐして0本発明の起泡性成形物は簡易Vこ得られるが
、その成形物の保存安定性は格別顕著に優れ1側法ば9
通常の厚さ100μ稈度のポリエチレン製袋中・常温の
室内に密封保°存するときけ24ケ月以上も変質が起ら
ず9袋が分解発生ガスによって膨らむこともない。しか
も長期保存後に水中に投入しても良好な起泡性を示し。
Although the foamable molded product of the present invention can be easily obtained, the storage stability of the molded product is exceptionally excellent.
When stored in a regular polyethylene bag with a thickness of 100 μm and sealed indoors at room temperature, no deterioration occurs for more than 24 months, and the bag does not swell due to gas generated by decomposition. Furthermore, it shows good foaming properties even when placed in water after long-term storage.

完全に水に溶解し、水が濁ることもない。It dissolves completely in water and does not make the water cloudy.

以下、比較例と共に実施例を挙げて更に詳しく説明する
が9本発明の技術的11Ii!囲はこれに限定されない
9 Technical 11Ii of the present invention! The enclosure is not limited to this.

実施例1〜7 粒径02〜1.1mm、含水率1.4チ以下の配合成分
と1粒径0.04−0.5 mm 、含水率0.2%以
下の酸化硼素を第1表記載の組成に配合し、V型プレン
ダーを使用して均一に混合した後、打錠機を使用して2
00にダ/cMの圧力で打錠し、直径20mm厚さ10
m1llの錠剤を成形した。この錠剤は1錠が52であ
る。
Examples 1 to 7 Compounding ingredients with a particle size of 02 to 1.1 mm and a moisture content of 1.4 mm or less and boron oxide with a particle size of 0.04 to 0.5 mm and a moisture content of 0.2% or less in Table 1 After blending into the stated composition and mixing uniformly using a V-type blender, 2.
Compressed into tablets at a pressure of 0.00 cm/cm, 20 mm in diameter and 10 mm in thickness.
ml tablets were molded. One tablet of this tablet weighs 52.

次いで、この得られた錠剤1箇を、縦・横50mm×6
0mmの4層ラミネート袋(ポリエステルに415 t
t 、ポリエチレン層12μ、アルミニウム/1v10
μ、ポリエチレン層30μが順次外側から内側ヘラミネ
ートされている。)に充填し。
Next, one of the obtained tablets was placed in a size of 50 mm x 6 mm in length and width.
0mm 4-layer laminated bag (415t on polyester)
t, polyethylene layer 12μ, aluminum/1v10
.mu., a polyethylene layer of 30 .mu. is sequentially laminated from the outside to the inside. ).

脱気後熱シールによυ密封包装した。引きつづき、この
包装物を恒温槽内45℃の空気中[40日間静置保存し
た後、取り田して袋の外観、特に膨張度合いを観察した
ところ第1表記載の結果が得られた。いずれも実用上充
分な安定性を示すことが認められる。更に、上記保存後
の錠剤を袋内から取り出し、水中に投入したところ。
After degassing, it was sealed and packaged by heat sealing. Subsequently, this package was stored in air at 45°C in a thermostatic oven for 40 days, and then removed and the appearance of the bag, especially the degree of expansion, was observed, and the results shown in Table 1 were obtained. All of them are recognized to exhibit sufficient stability for practical use. Furthermore, the tablets after storage were taken out of the bag and put into water.

良好な起泡性を示した。It showed good foaming properties.

比較例1〜6 酸化硼素を加えないで、第1表記載の組成で配合した他
は実施例1と同様にして錠剤を成形し、更に保存試験を
行なったところ、第1表記載の結果が得られた。いずれ
も分5ψFガス発生による袋の膨張、或いは袋の破裂が
起こり、到底実用に供し得ないことが認めらhろ。
Comparative Examples 1 to 6 Tablets were molded in the same manner as in Example 1 except that boron oxide was not added and the composition shown in Table 1 was used, and a storage test was conducted. The results shown in Table 1 were obtained. Obtained. In either case, the bag expands or ruptures due to the generation of 5ψF gas, making it impossible to put it to practical use.

第  1  表 (え1コ)米−I  DC!0−44aは2クロロイソ
シアヌル酸ナトリウムを表わす。
Table 1 (E1) Rice-I DC! 0-44a represents sodium dichloroisocyanurate.

半一2  PSKはパーオキシ硫酸水素カリウムを表わ
す。
Half-2 PSK stands for potassium peroxybisulfate.

米−5袋の保存状態 ○;保存の前後で不変口;わずか
に膨張 Δ;明らかに膨張 ×;著しい膨張 ≠;袋の破裂 実施例8〜12 粒径、含水率共に前記実施例に記載のものと同じである
配合成分を第2表記載の組成とし。
Storage condition of rice-5 bags ○; Mouth unchanged before and after storage; Slight expansion Δ; Obvious expansion ×; Significant expansion ≠; Bag rupture Examples 8 to 12 Particle size and moisture content are both the same as described in the previous example. The same ingredients as those listed in Table 2 were used.

前記実施例と同様にして1錠5yの錠剤を成形した。One 5y tablet was molded in the same manner as in the previous example.

次いで、この錠剤1箇を、*+横40mmX50mmの
厚ざ120μの高密度ポリエチレン製袋に充填し、脱気
後熱シールによυ密封包装した。
Next, one tablet was filled into a high-density polyethylene bag measuring 40 mm x 50 mm and 120 μm in thickness, and after degassing, the bag was sealed and packaged by heat sealing.

引きつづき、この包装物を35°C相対湿度70チの恒
温恒湿槽内に15日間静置保存し牟後取り出し袋の外観
を観察したところ、第2表記載の結果を得た。いずれも
充分な安定性を示すことが認められる。更に、上記保存
後の錠剤は。
Subsequently, this package was stored for 15 days in a constant temperature and humidity chamber at 35° C. and a relative humidity of 70° C. After storage, the appearance of the bag was observed, and the results shown in Table 2 were obtained. All were found to exhibit sufficient stability. Furthermore, the tablets after storage are as follows.

水中でも良好な起泡性を示した。It showed good foaming properties even in water.

比較例8〜12 第2表記載の配合組成とした他は、実施例8〜12と同
様にして錠剤を成形し、更に保存性を試験したところ第
2表記載の結果を得た。酸化硼素による安定化効果を欠
如していることが明らかに認められる、 第  2  表 特許出願人 日産化学工業株式会社
Comparative Examples 8 to 12 Tablets were molded in the same manner as in Examples 8 to 12, except that the formulation compositions shown in Table 2 were used, and the preservability was tested, and the results shown in Table 2 were obtained. Table 2 Patent applicant Nissan Chemical Industries, Ltd., which clearly lacks the stabilizing effect of boron oxide

Claims (1)

【特許請求の範囲】[Claims] 過酸化水素付加化合物100重量部と塩素化インシアヌ
ール酸、パーオキシ硫酸塩若しくはパーオキシ硫酸水素
塩4〜500重量部を含む粉状配合物又はアルカリ金属
炭酸塩若しくはアルカリ金属重炭酸塩100重量部と固
体の有機酸若しくは無機酸10〜100重量部を含む粉
状配合物の100重量部に酸化硼素を0.1〜30重量
部を加え加圧成形したことを特徴とする起泡性成形物。
A powder formulation comprising 100 parts by weight of a hydrogen peroxide addition compound and 4 to 500 parts by weight of chlorinated incyanuric acid, peroxysulfate or peroxyhydrogensulfate or 100 parts by weight of an alkali metal carbonate or alkali metal bicarbonate and a solid 1. A foamable molded article, characterized in that 0.1 to 30 parts by weight of boron oxide is added to 100 parts by weight of a powdery compound containing 10 to 100 parts by weight of an organic acid or an inorganic acid, and the mixture is pressure-molded.
JP13930082A 1982-08-11 1982-08-11 foamable molded product Expired JPS6019946B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13930082A JPS6019946B2 (en) 1982-08-11 1982-08-11 foamable molded product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13930082A JPS6019946B2 (en) 1982-08-11 1982-08-11 foamable molded product

Publications (2)

Publication Number Publication Date
JPS5930879A true JPS5930879A (en) 1984-02-18
JPS6019946B2 JPS6019946B2 (en) 1985-05-18

Family

ID=15242068

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13930082A Expired JPS6019946B2 (en) 1982-08-11 1982-08-11 foamable molded product

Country Status (1)

Country Link
JP (1) JPS6019946B2 (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60176904A (en) * 1984-02-20 1985-09-11 Nishi Akizo Solid agent for generating oxygen, and its preparation
JPS61192800A (en) * 1985-02-20 1986-08-27 四国化成工業株式会社 Production of foamable cleanser
JPS61228100A (en) * 1985-04-01 1986-10-11 株式会社ソフト九九コーポレーション Foamable detergent composition
JPS62182389A (en) * 1986-02-05 1987-08-10 清水建設株式会社 Method and device for forming blasting hole
JPH02125088A (en) * 1988-07-15 1990-05-14 Onoda:Kk Groove forming tool for brittle object and crushing method for brittle object
JPH04158200A (en) * 1990-10-23 1992-06-01 Yuichi Nakamura Fissure control exploding method
US5232701A (en) * 1990-10-11 1993-08-03 Sumitomo Chemical Company, Limited Boron carbonate and solid acid pesticidal composition
WO1997035955A1 (en) * 1996-03-22 1997-10-02 Alfred Kärcher GmbH & Co. Cleaning concentrate
JP2002356700A (en) * 2001-05-31 2002-12-13 Ue Ruko:Kk Foaming washing tool and method
JP2018104331A (en) * 2016-12-26 2018-07-05 ホーユー株式会社 Percarbonate packaging bag

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60176904A (en) * 1984-02-20 1985-09-11 Nishi Akizo Solid agent for generating oxygen, and its preparation
JPS61192800A (en) * 1985-02-20 1986-08-27 四国化成工業株式会社 Production of foamable cleanser
JPH0347318B2 (en) * 1985-02-20 1991-07-18 Shikoku Chem
JPS61228100A (en) * 1985-04-01 1986-10-11 株式会社ソフト九九コーポレーション Foamable detergent composition
JPS62182389A (en) * 1986-02-05 1987-08-10 清水建設株式会社 Method and device for forming blasting hole
JPH0578634B2 (en) * 1986-02-05 1993-10-29 Shimizu Construction Co Ltd
JPH02125088A (en) * 1988-07-15 1990-05-14 Onoda:Kk Groove forming tool for brittle object and crushing method for brittle object
US5232701A (en) * 1990-10-11 1993-08-03 Sumitomo Chemical Company, Limited Boron carbonate and solid acid pesticidal composition
JPH04158200A (en) * 1990-10-23 1992-06-01 Yuichi Nakamura Fissure control exploding method
WO1997035955A1 (en) * 1996-03-22 1997-10-02 Alfred Kärcher GmbH & Co. Cleaning concentrate
JP2002356700A (en) * 2001-05-31 2002-12-13 Ue Ruko:Kk Foaming washing tool and method
JP2018104331A (en) * 2016-12-26 2018-07-05 ホーユー株式会社 Percarbonate packaging bag

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