JPH0466203B2 - - Google Patents
Info
- Publication number
- JPH0466203B2 JPH0466203B2 JP58220236A JP22023683A JPH0466203B2 JP H0466203 B2 JPH0466203 B2 JP H0466203B2 JP 58220236 A JP58220236 A JP 58220236A JP 22023683 A JP22023683 A JP 22023683A JP H0466203 B2 JPH0466203 B2 JP H0466203B2
- Authority
- JP
- Japan
- Prior art keywords
- isocyanuric acid
- chlorinated isocyanuric
- sodium
- granules
- hydrogen peroxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 150000007973 cyanuric acids Chemical class 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 18
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 15
- 239000002245 particle Substances 0.000 claims description 9
- 238000005469 granulation Methods 0.000 claims description 7
- 230000003179 granulation Effects 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 3
- 238000000034 method Methods 0.000 description 17
- 239000008187 granular material Substances 0.000 description 12
- -1 hydrogen peroxide compound Chemical class 0.000 description 12
- 239000007789 gas Substances 0.000 description 10
- 238000002156 mixing Methods 0.000 description 9
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 239000004088 foaming agent Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 238000004806 packaging method and process Methods 0.000 description 5
- 239000004604 Blowing Agent Substances 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000011973 solid acid Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000005001 laminate film Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- FHHJDRFHHWUPDG-UHFFFAOYSA-L peroxysulfate(2-) Chemical compound [O-]OS([O-])(=O)=O FHHJDRFHHWUPDG-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Description
本発明は保存中に、ガス発生により包装袋の膨
張、または破裂等を生起しない安定性の優れた発
泡性造粒組成物の製造法に関する。
従来より、水中に投入した際に炭酸ガスを発生
しながら、短時間に溶解する錠剤が医薬または食
品分野等に見られる。これらの発泡剤は重炭酸ナ
トリウムに固体の酸を混合するか、過炭酸ソー
ダ、過硼酸ソーダの如き過酸化水素付加化合物に
ペルオキシ硫酸塩、ペルオキシ硫酸水素塩を混合
した粉体が知られている。また前記の過酸化水素
付加化合物に対して、塩素化イソシアヌル酸を配
合した組成物も発泡剤として知られ、家庭用の風
呂水清浄剤、義歯洗浄剤、台所(俎、分布)用、
オムツ用、更にペツト用の脱臭剤に至るまで、そ
の用途は極めて広く有用である。
しかるに上記塩素化イソシアヌル酸を配合した
発泡剤は極めて水分に敏感であり、この為に原
料、製品の取扱い、保存は細心の注意を必要とす
る。例えば、上記気泡剤を含む粉、顆粒または錠
剤を外気に曝す場合、外気より水分を吸収し、そ
れ相当のガスを発生することにより、もはや使用
時の発泡性が乏しくなるだけでなく、殺菌、漂
白、脱臭等に有効な活性有効酸素または活性有効
塩素の濃度が低下する。これを防ぐ為、通常は発
泡剤をアルミのラミネートフイルムの如き密閉包
装に充填している。然し包装前に吸収した水分に
よりガスが発生し包装袋が膨張したり極端な場合
は破裂する事もある。この様な発泡剤の敏感さに
対し、かかる問題点の解決を意図した提案が幾つ
か見られるが、まだ充分なものが得られていな
い。
例えば、重炭酸ナトリウムと固体酸を用いた発
泡剤の場合、錠剤に於いては多層錠にしたり、特
公昭58−24361号公報では、過酸化水素付加化合
物を炭酸酸ナトリウム、硫酸ナトリウムで表面被
覆する方法等が提案されているがこれらは、使用
時水中での発泡が不充分でまた表面被覆処理はか
なりコストが高くなる。
また特公昭58−101199号公報では塩素化イソシ
アヌル酸の長期間の保存に於いてアルミニウム/
ポリエチレンラミネート包装袋が塩素化イソシア
ヌル酸から発生する分解塩素ガスによつて腐食を
受けることを抑える方法として結晶水を含まな
い、無水のゼオライトを混合することで、達成で
きることを提案している。しかし本方法は過酸化
水素付加化合物と混合した塩素化イソシアヌル酸
の系からの分解ガスの発生を抑える効果は全くな
く、またゼオライトそのものが水に対して不溶解
であるために使用分野が限定され好ましくない。
以上の点を鑑み本研究者らは鋭意研究の結果、
以外にも、前記の発泡剤組成物に於いて塩素化イ
ソシアヌル酸の粒子径をある程度以上に大きく
し、発泡性造粒組成物を得ると極めて安定で、分
解酸素ガスの発生も一定値で停止する事を見出し
た。
即ち、本発明は過酸化水素付加化合物と塩素化
イソシアヌル酸を必須2成分とする発泡性造粒組
成物の製法於いて、造粒の際の原料に塩素化イソ
シアヌル酸の粒径が75〜1000μである塩素化イソ
シアヌル酸を用いる事を特徴とする保存安定性の
ある発泡性造粒組成物の製造法である。
本発明に於ける塩素化イソシアヌル酸とは塩素
化イソシアヌル酸ナトリウム、塩素化イソシアヌ
ル酸カリウム等の塩素化イソシアヌル酸のアルカ
リ金属塩を云い、実際上、水分は可能な限り少な
無水物が好ましい。
本発明の発泡剤造粒組成物の形態は顆粒あるい
は錠剤であり、造粒方法は公知の方法で良いが、
造粒の際の原料に粒径が75〜1000μの塩素化イソ
シアヌル酸と他の配合成分を均一に混合した配合
物を使用する事が必要である。工業的には前記の
配合物を加圧ロールにより圧縮造粒し顆粒を得る
方法が好ましい。また錠剤を得る時も同様に粒径
が75μ〜1000μの塩素化イソシアヌル酸と他の配
合成分を均一に混合した配合物を用いる方法と、
また前記の顆粒を用いて打錠する方法がある。
本発明方法に於いて使用する塩素化イソシアヌ
ル酸の粒径は75μ〜1000μの範囲が90%以上であ
り好ましくは150μ〜700μの範囲が90%以上であ
る。塩素化イソシアヌル酸の粒径が75μ以下では
発泡剤造粒組成物の安定性が低く、1000μ以上で
は過酸化水素付加化合物との混合が不均一にな
り、特に顆粒や小型の錠剤を成型する場合に於い
て偏析が生じ好ましくない。塩素化イソシアヌル
酸以外の配合物は粉体、または顆粒のいずれでも
良い。
本発明に於いて使過する酸化水素付加化合物と
しては特に過酸化ソーダ、過硼酸ソーダの1水塩
が好ましい。
本発明の必須成分である過酸化水素付加化合物
と塩素化イソシアヌル酸の混合割合は過酸化水素
付加化合物100重量部に対して塩素化イソシアヌ
ル酸を5〜500重量部が発泡性を付与するために
好ましい。これ以外の範囲では発泡性が低い。更
に、造粒の際に必要に応じて硫酸ナトリウム、珪
酸ナトリウム、燐酸ナトリウム等のアルカリビル
ダーや、マンニツト、乳糖等の結合剤、ラウリル
硫酸ナトリウム、α−オレフインスルホン酸ナト
リウム等の界面活性剤、色素、香料、更にはポリ
エチレングリコール、ステアリン酸塩、タルク等
の成型助剤を添加することが好ましい。
上記の方法で得た発泡性造粒組成物は分解ガス
の発生が少なく一定値で停止するため、保存中に
ガス発生による包装袋の膨張、または破裂が起こ
らず保存安定性が優れている。
以下に実施例、比較例をもつて詳しく説明する
が、本発明の技術的範囲はこれに限定されるもの
でない。
先ず、配合に使用した原料、顆粒化方法、打錠
方法及び得られた造粒物の評価方法を述べる。
表1に使用した過酸化水素付加化合物と塩素化
イソシアヌル酸を示す。
The present invention relates to a method for producing a highly stable foamable granulated composition that does not cause expansion or rupture of packaging bags due to gas generation during storage. BACKGROUND ART Conventionally, tablets that dissolve in a short time while generating carbon dioxide gas when placed in water have been found in the pharmaceutical and food fields. These blowing agents are known as powders made by mixing sodium bicarbonate with a solid acid, or by mixing peroxysulfate or peroxyhydrogensulfate with a hydrogen peroxide addition compound such as sodium percarbonate or sodium perborate. . Compositions containing chlorinated isocyanuric acid in addition to the above-mentioned hydrogen peroxide compound are also known as foaming agents, and are used as household bath water cleaners, denture cleaners, kitchen cleaners, etc.
Its uses are extremely wide and useful, from diapers to pet deodorizers. However, the blowing agent containing the above-mentioned chlorinated isocyanuric acid is extremely sensitive to moisture, and therefore, the raw materials and products must be handled and stored with great care. For example, when powders, granules, or tablets containing the above-mentioned foaming agents are exposed to the outside air, they absorb moisture from the outside air and generate a corresponding amount of gas, which not only results in poor foaming properties during use, but also sterilization and The concentration of active oxygen or active chlorine, which is effective for bleaching, deodorization, etc., decreases. To prevent this, the foaming agent is usually packed in a sealed package such as an aluminum laminate film. However, the moisture absorbed before packaging generates gas that can cause the packaging bag to expand or, in extreme cases, burst. Regarding the sensitivity of blowing agents, there have been several proposals aimed at solving these problems, but nothing satisfactory has yet been achieved. For example, in the case of an effervescent agent using sodium bicarbonate and a solid acid, tablets are made into multilayer tablets, and in Japanese Patent Publication No. 58-24361, a hydrogen peroxide adduct is surface-coated with sodium carbonate and sodium sulfate. Although methods have been proposed to do this, foaming in water during use is insufficient, and surface coating treatment is quite costly. Furthermore, in Japanese Patent Publication No. 1983-101199, aluminum/
As a method of suppressing corrosion of polyethylene laminate packaging bags by decomposed chlorine gas generated from chlorinated isocyanuric acid, we have proposed that this can be achieved by mixing anhydrous zeolite, which does not contain water of crystallization. However, this method has no effect on suppressing the generation of decomposed gas from the system of chlorinated isocyanuric acid mixed with a hydrogen peroxide compound, and the field of use is limited because zeolite itself is insoluble in water. Undesirable. In view of the above points, the present researchers conducted intensive research and found that
In addition, if the particle size of the chlorinated isocyanuric acid in the above-mentioned foaming agent composition is increased to a certain level or more to obtain a foamable granulated composition, it will be extremely stable and the generation of decomposed oxygen gas will stop at a certain value. I found something to do. That is, the present invention provides a method for producing a foamable granulated composition containing a hydrogen peroxide compound and chlorinated isocyanuric acid as two essential components, in which the particle size of chlorinated isocyanuric acid is 75 to 1000 μm as a raw material during granulation. This is a method for producing a storage-stable foamable granulated composition characterized by using chlorinated isocyanuric acid. In the present invention, chlorinated isocyanuric acid refers to alkali metal salts of chlorinated isocyanuric acid such as sodium chlorinated isocyanurate and potassium chlorinated isocyanurate, and in practice, anhydride with as little water content as possible is preferred. The foaming agent granulated composition of the present invention is in the form of granules or tablets, and the granulation method may be any known method.
It is necessary to use a mixture of chlorinated isocyanuric acid with a particle size of 75 to 1000μ and other ingredients uniformly mixed as a raw material for granulation. Industrially, a method of obtaining granules by compressing and granulating the above-mentioned blend using a pressure roll is preferred. In addition, when obtaining tablets, a method in which a mixture of chlorinated isocyanuric acid with a particle size of 75μ to 1000μ and other ingredients is uniformly mixed is used;
There is also a method of tabletting using the above granules. The particle size of the chlorinated isocyanuric acid used in the method of the present invention is 90% or more in the range of 75μ to 1000μ, preferably 90% or more in the range of 150μ to 700μ. If the particle size of chlorinated isocyanuric acid is less than 75μ, the stability of the blowing agent granulation composition is low, and if it is more than 1000μ, mixing with the hydrogen peroxide compound becomes uneven, especially when molding granules or small tablets. Segregation occurs, which is undesirable. The ingredients other than chlorinated isocyanuric acid may be in the form of powder or granules. As the hydrogen oxide addition compound used in the present invention, sodium peroxide and sodium perborate monohydrate are particularly preferred. The mixing ratio of the hydrogen peroxide compound and chlorinated isocyanuric acid, which are essential components of the present invention, is such that 5 to 500 parts by weight of chlorinated isocyanuric acid is added to 100 parts by weight of the hydrogen peroxide compound to impart foaming properties. preferable. Foamability is low in other ranges. Furthermore, during granulation, alkali builders such as sodium sulfate, sodium silicate, and sodium phosphate, binders such as mannitrate and lactose, surfactants such as sodium lauryl sulfate and sodium α-olefin sulfonate, and pigments are added as necessary. It is preferable to add molding aids such as , fragrance, and furthermore polyethylene glycol, stearate, and talc. The foamable granulated composition obtained by the above method generates less decomposed gas and stops at a constant value, so the packaging bag does not expand or burst due to gas generation during storage, and has excellent storage stability. The present invention will be explained in detail below using Examples and Comparative Examples, but the technical scope of the present invention is not limited thereto. First, the raw materials used for compounding, the granulation method, the tableting method, and the evaluation method of the obtained granules will be described. Table 1 shows the hydrogen peroxide adduct and chlorinated isocyanuric acid used.
【表】【table】
ロール;径160mm 幅60mm
フレークの厚み:2.3〜3.2mm
ロール回転数;15rpm
油圧;87Kg/cm2、線圧;1.5t/cm
錠剤の製法
前記の方法により顆粒を得、この顆粒を直径20
mmの臼に2.0gを充填した後、その上に杵を入れ、
油圧プレスにより面圧が600Kg/cm2の圧力をかけ、
圧縮成型して径が20mm、厚みが3.8mmの錠剤を得
る。
安定性の評価方法
ポリエチレンテレフタレート/ポリエチレン/
アルミニウム/ポリエチレンよりなるアルミニウ
ムラミネートシート(厚さ;20/15/12/30μ)
5cmX5cmを二枚重ねて三方を熱シールして小袋
をつくり、この袋に顆粒2g、または錠剤1錠
(2g)を入れた後に熱シールして閉じる。その
後、四隅の内の一つに注射針をさして中の空気を
完全に抜き、針穴は熱シールして閉じる。このよ
うにして作製したアルミ袋に充填した顆粒、また
は錠剤を55℃の恒温槽に1週間入れて、1週間経
過後アルミ袋内のガス(酸素)を注射により採取
し、その発生量を求める。
実施例1〜10及び比較例1〜6
表2に示す配合比で前記方法により配合し、顆
粒状の発泡性造粒組成物を製造し、上記の安定性
の評価方法で安定性の評価を行つた。安定性の評
価結果も併せて表2に示す。
Roll; Diameter: 160 mm Width: 60 mm Flake thickness: 2.3 to 3.2 mm Roll rotation speed: 15 rpm Oil pressure: 87 Kg/cm 2 , linear pressure: 1.5 t/cm Tablet manufacturing method Granules were obtained by the above method, and the granules were made into a diameter of 20 mm.
After filling a mm mortar with 2.0g, put a pestle on top of it,
A pressure of 600 kg/cm 2 is applied using a hydraulic press.
Compression molding yields tablets with a diameter of 20 mm and a thickness of 3.8 mm. Stability evaluation method Polyethylene terephthalate/Polyethylene/
Aluminum laminate sheet made of aluminum/polyethylene (thickness: 20/15/12/30μ)
Make a small bag by stacking two 5cm x 5cm sheets and heat sealing on three sides, put 2g of granules or 1 tablet (2g) into this bag, then heat seal and close. Then, insert a syringe needle into one of the four corners to remove the air completely, and heat seal the needle hole to close it. The granules or tablets filled in the aluminum bag prepared in this way are placed in a constant temperature bath at 55℃ for one week, and after one week, the gas (oxygen) inside the aluminum bag is collected by injection to determine the amount generated. . Examples 1 to 10 and Comparative Examples 1 to 6 A granular foamable granulated composition was produced by blending according to the above method at the blending ratio shown in Table 2, and the stability was evaluated using the above stability evaluation method. I went. The stability evaluation results are also shown in Table 2.
【表】【table】
【表】
表2に示すように本発明方法の塩素化イソシア
ヌル酸は75μ以上の粒径を用い他の配合成分と混
合し顆粒化したほうが、比較例の粉末の塩素化イ
ソシアヌル酸を用いる時よりガスの発生量が少な
く安定性が良い。
実施例11〜12及び比較例7〜8
表2に示す配合比で前記方法により配合し、顆
粒状の発泡性造粒組成物を製造し、打錠し錠剤を
得た。この錠剤の安定性の評価結果を表3に併せ
て示す。[Table] As shown in Table 2, it is better to use chlorinated isocyanuric acid in the method of the present invention with a particle size of 75μ or more, mix it with other ingredients, and granulate it than to use powdered chlorinated isocyanuric acid in the comparative example. The amount of gas generated is small and the stability is good. Examples 11-12 and Comparative Examples 7-8 A granular effervescent granulated composition was produced by blending according to the method described above at the blending ratio shown in Table 2, and was compressed to obtain a tablet. The stability evaluation results of this tablet are also shown in Table 3.
【表】
表2に示すように本発明方法の塩素化イソシア
ヌル酸は75μ以上の粒径を用い他の配合成分と混
合し錠剤化したほうが、比較例の粉末の塩素化イ
ソシアヌル酸を用いる時よりガスの発生量が少な
く安定性が良い。[Table] As shown in Table 2, it is better to use chlorinated isocyanuric acid in the method of the present invention with a particle size of 75μ or more, mix it with other ingredients, and form tablets than to use powdered chlorinated isocyanuric acid in the comparative example. The amount of gas generated is small and the stability is good.
Claims (1)
酸を必須2成分とする発泡性造粒組成物の製法於
いて、造粒の際の原料に粒径が75〜1000μである
塩素化イソシアヌル酸を用いる事を特徴とする保
存安定性のある発泡性造粒組成物の製造法。1. In the method of manufacturing a foamable granulated composition containing a hydrogen peroxide addition compound and chlorinated isocyanuric acid as two essential components, chlorinated isocyanuric acid having a particle size of 75 to 1000 μ is used as a raw material during granulation. A method for producing a storage-stable foamable granulated composition characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58220236A JPS60112714A (en) | 1983-11-22 | 1983-11-22 | Production of foamable granular composition having storage stability |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58220236A JPS60112714A (en) | 1983-11-22 | 1983-11-22 | Production of foamable granular composition having storage stability |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60112714A JPS60112714A (en) | 1985-06-19 |
JPH0466203B2 true JPH0466203B2 (en) | 1992-10-22 |
Family
ID=16748022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58220236A Granted JPS60112714A (en) | 1983-11-22 | 1983-11-22 | Production of foamable granular composition having storage stability |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60112714A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0622453A1 (en) * | 1993-04-26 | 1994-11-02 | Setric International S.A. | Process for particulate protection of a combustible product against the action of a chlorinated product mixed therewith |
JP2002356700A (en) * | 2001-05-31 | 2002-12-13 | Ue Ruko:Kk | Foaming washing tool and method |
CA2759344C (en) * | 2011-08-31 | 2016-10-11 | DeVere Company, Inc. | Antimicrobial surface treatment composition comprising a peroxygen compound, a chlorinated isocyanurate salt, and a bleach activator |
JP6735663B2 (en) * | 2016-12-26 | 2020-08-05 | ホーユー株式会社 | Percarbonate packaging bag |
-
1983
- 1983-11-22 JP JP58220236A patent/JPS60112714A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS60112714A (en) | 1985-06-19 |
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