JPH0335359B2 - - Google Patents
Info
- Publication number
- JPH0335359B2 JPH0335359B2 JP56199712A JP19971281A JPH0335359B2 JP H0335359 B2 JPH0335359 B2 JP H0335359B2 JP 56199712 A JP56199712 A JP 56199712A JP 19971281 A JP19971281 A JP 19971281A JP H0335359 B2 JPH0335359 B2 JP H0335359B2
- Authority
- JP
- Japan
- Prior art keywords
- sodium
- zeolite
- bleach
- aluminum
- present
- 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
- 239000000203 mixture Substances 0.000 claims description 16
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 15
- 239000000460 chlorine Substances 0.000 claims description 15
- 229910052801 chlorine Inorganic materials 0.000 claims description 15
- 229910021536 Zeolite Inorganic materials 0.000 claims description 14
- 239000007844 bleaching agent Substances 0.000 claims description 14
- 239000010457 zeolite Substances 0.000 claims description 14
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 13
- CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical compound ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 claims description 8
- 239000013078 crystal Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- IFIDXBCRSWOUSB-UHFFFAOYSA-N potassium;1,3-dichloro-1,3,5-triazinane-2,4,6-trione Chemical compound [K+].ClN1C(=O)NC(=O)N(Cl)C1=O IFIDXBCRSWOUSB-UHFFFAOYSA-N 0.000 claims description 4
- JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 9
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 238000004806 packaging method and process Methods 0.000 description 6
- 239000011734 sodium Substances 0.000 description 5
- -1 sodium alkyl sulfate Chemical class 0.000 description 5
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 235000019645 odor Nutrition 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000001488 sodium phosphate Substances 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- 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 2
- 239000004698 Polyethylene Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000000645 desinfectant Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 description 1
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- 241001391944 Commicarpus scandens Species 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 241001237745 Salamis Species 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000015175 salami Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960001790 sodium citrate Drugs 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 1
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 description 1
- 229940039790 sodium oxalate Drugs 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000001433 sodium tartrate Substances 0.000 description 1
- 229960002167 sodium tartrate Drugs 0.000 description 1
- 235000011004 sodium tartrates Nutrition 0.000 description 1
- QHFDHWJHIAVELW-UHFFFAOYSA-M sodium;4,6-dioxo-1h-1,3,5-triazin-2-olate Chemical compound [Na+].[O-]C1=NC(=O)NC(=O)N1 QHFDHWJHIAVELW-UHFFFAOYSA-M 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
- 230000009182 swimming Effects 0.000 description 1
- 229950009390 symclosene Drugs 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 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
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Description
本発明は水溶液中で次亜塩素酸又は次亜塩素酸
塩を生成する粉末塩素系標白剤の安定化組成物に
関する。
次亜塩素酸又は次亜塩素酸塩を水溶液中で生成
する粉末塩素系漂白剤は、その良好な漂白性能、
殺菌性能の故に、家庭用衣類の漂白、浄化槽、プ
ールの殺菌等の用途に使用されており、これら漂
白剤としてはトリクロルイソシアヌール酸、ジク
ロルイソシアヌール酸、ジクロルイソシアヌール
酸カリウム、ジクロルイソシアヌール酸ナトリウ
ム、ジクロロジメチルヒダントイン、テトラクロ
ログルコルリル或いはサラシ粉等がある。
しかし、これら粉末塩素系漂白剤は、保存時の
安定性に乏しく、分解して塩素ガスを発生する。
その結果、刺激臭、アレルギー等、人体への好ま
しくない影響、および包装容器の腐蝕等の不都合
を生じる。そこで、ジクロルイソシアヌール酸、
ジクロルイソシアヌール酸カリウム、ジクロルイ
ソシアヌール酸ナトリウム等が安定性の点で優れ
ている点から、工業的に大量生産されている。し
かし、これらの物質も尚、安定性は十分でないた
め、特定の香料、メラミン等の安定剤を添加する
提案がなされてきた。しかしながら、これら安定
剤を添加しても尚、塩素系漂白剤の安定化は十分
とはいえず、家庭用漂白剤等、大衆消費者のため
の商品には到庭使用できるものではない。たとえ
ば、これら粉末塩素系漂白剤は粉末状で使用して
もよいが、1回の使用分だけ錠剤にして用いると
便利である。これらの錠剤は一錠一錠をアルミニ
ユウム/ポリエチレンラミネート包装しておけば
外部からの吸湿もなく好ましい。しかしながら余
り長期間保存するとアルミニウムが腐蝕を受け小
孔を生成しその後は安定性を低下する様になる。
本発明者らは粉末塩素系漂白剤の安定化につい
て鋭意検討した結果合成結晶型A型ゼオライトを
添加することにより顕著な安定化効果の得られる
ことを見い出し本発明に到達した。
即ち、本発明はジクロルイソシアヌール酸ナト
リウム、ジクロルイソシアヌール酸カリウム及び
ジクロルイソシアヌール酸からなる群からばれた
1種又は2種以上の粉末塩素系漂白剤と、含成結
晶型A型ゼオライトとを重量比で97/3〜70/30
の割合で含有することを特徴とする粉末塩素系漂
白剤の安定化組成物を提供するものである。
本発明に用いられるA型ゼオライトは合成結晶
型で、次の式で示される骨格構造を持つものであ
る。
6{(Na2O)・(Al2O3)・2(SiO2)}
ゼオライトは一般的には結晶水を持ち飽和された
状態で3〜25重量%の水分を持つことになる。こ
の様な含水ゼオライトを用いてもよいが、好まし
くは飽和水和水以下の結晶水、更に好ましくは結
晶水を含まないゼオライトがよい。
本発明組成物中の塩素系漂白剤とA型ゼオライ
トとの重量比率は97/3〜70/30の範囲で選択さ
れる。即ちゼオライトの量が少ないと十分効果が
なく、又多くても無駄になるだけである。本発明
の組成物を製造するに当つては特に限定するもの
ではないが粉末塩素系漂白剤、ゼオライトの粒度
を16meshフルイ通過が95%以上のものを用いる
ことが好ましい。
本発明の組成物には更に必要に応じて、硫酸ナ
トリウム、重炭酸ナトリウム、炭酸ナトリウム、
トリボリリン酸ナトリウム、ピロリン酸ナトリウ
ム、リン酸一ナトリウム、リン酸二ナトリウム、
リン酸三ナトリウムの如き希釈剤としての無機
塩、クエン酸ナトリウム、修酸ナトリウム、酒石
酸ナトリウム、コハク酸ナトリウム、ニトリロト
リ酢酸ナトリウム、エチレンジアミン四酢酸ナト
リウム、ポリエチレングリコール(分子量2000〜
20000)、カルボキシメチルセルロースナトリウム
塩、ヒドロキシエチルセルロース、アルキルベン
ゼンスルホン酸ナトリウム、アルキル硫酸ナトリ
ウム、アルキルスルホン酸ナトリウム、ポリエチ
レングリコールアルキルエーテル、ポリエチレン
グリコールアルキルフエノールエーテル等の有機
酸塩、高分子化合物金属キレート剤、陰イオン性
界面活性剤、非イオン性界面活性剤等々、更には
香料、顔料、染料等々、漂白剤、漂白洗剤、浄化
槽殺菌剤、プール用殺菌剤等の用途に対する製品
をつくるための常用成分を添加することができ
る。
以下、、実施例により本発明を更に詳細に説明す
る。尚、例中の部は重量基準である。
実施例 1
The present invention relates to a composition for stabilizing a powdered chlorine whitening agent that produces hypochlorous acid or hypochlorite in aqueous solution. Powdered chlorine bleach that produces hypochlorous acid or hypochlorite in an aqueous solution has good bleaching performance,
Because of its sterilizing properties, it is used for purposes such as bleaching household clothes, sterilizing septic tanks, and swimming pools. These bleaching agents include trichloroisocyanuric acid, dichloroisocyanuric acid, potassium dichloroisocyanurate, and dichloroisocyanurate. Examples include sodium isocyanurate, dichlorodimethylhydantoin, tetrachloroglucoruril, and salami powder. However, these powdered chlorine bleaches have poor stability during storage and decompose to generate chlorine gas.
As a result, undesirable effects on the human body such as irritating odors and allergies, and inconveniences such as corrosion of packaging containers occur. Therefore, dichloroisocyanuric acid,
Potassium dichloroisocyanurate, sodium dichloroisocyanurate, and the like are industrially produced in large quantities because of their excellent stability. However, since these substances still do not have sufficient stability, proposals have been made to add certain fragrances and stabilizers such as melamine. However, even with the addition of these stabilizers, the stabilization of chlorine bleach is still insufficient, and it cannot be used as a commercial product for mass consumers, such as household bleach. For example, these powdered chlorine bleaches may be used in powder form, but it is convenient to form them into tablets for one-time use. It is preferable for these tablets to be packaged one by one in aluminum/polyethylene laminate to avoid moisture absorption from the outside. However, if the aluminum is stored for too long, it will corrode and form small pores, which will subsequently reduce its stability. The inventors of the present invention have conducted extensive studies on the stabilization of powdered chlorine bleach, and have discovered that a significant stabilizing effect can be obtained by adding synthetic crystalline A-type zeolite, thereby achieving the present invention. That is, the present invention provides one or more powdered chlorine bleaches selected from the group consisting of sodium dichloroisocyanurate, potassium dichloroisocyanurate, and dichloroisocyanuric acid, and a crystal type A-containing bleach. Weight ratio of 97/3 to 70/30 with zeolite
The present invention provides a stabilizing composition for powdered chlorine bleach, characterized in that it contains a powdered chlorine bleach in a proportion of . The A-type zeolite used in the present invention is a synthetic crystal type and has a skeleton structure represented by the following formula. 6 {(Na 2 O)・(Al 2 O 3 )・2(SiO 2 )} Zeolite generally has water of crystallization and has a water content of 3 to 25% by weight in a saturated state. Although such a hydrous zeolite may be used, it is preferable to use a zeolite containing no crystal water, preferably less than saturated water of hydration, and more preferably a zeolite containing no crystal water. The weight ratio of chlorine bleach to type A zeolite in the composition of the present invention is selected within the range of 97/3 to 70/30. That is, if the amount of zeolite is small, it will not be sufficiently effective, and if the amount is large, it will just be wasted. In producing the composition of the present invention, although there are no particular limitations, it is preferable to use a powdered chlorine bleach and a zeolite having a particle size of 95% or more that passes through a 16 mesh sieve. The composition of the present invention may further include sodium sulfate, sodium bicarbonate, sodium carbonate,
Sodium tribolyphosphate, sodium pyrophosphate, monosodium phosphate, disodium phosphate,
Inorganic salts as diluents such as trisodium phosphate, sodium citrate, sodium oxalate, sodium tartrate, sodium succinate, sodium nitrilotriacetate, sodium ethylenediaminetetraacetate, polyethylene glycol (molecular weight from 2000 to
20000), carboxymethyl cellulose sodium salt, hydroxyethyl cellulose, sodium alkylbenzene sulfonate, sodium alkyl sulfate, sodium alkyl sulfonate, organic acid salts such as polyethylene glycol alkyl ether, polyethylene glycol alkyl phenol ether, polymer compound metal chelating agent, anion chemical surfactants, nonionic surfactants, etc., as well as fragrances, pigments, dyes, etc., as well as commonly used ingredients to make products for applications such as bleach, bleach detergent, septic tank disinfectant, pool disinfectant, etc. be able to. Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that parts in the examples are based on weight. Example 1
【表】
上記組成を有するA〜Eの5種の混合物を夫々
3gづつ錠剤に打錠し、アルミピロ包装に密封し
て20℃の恒温室に6ケ月間保存し、ピロ包装のア
ルミ面に生じる腐蝕を観察した。夫々のサンプル
30ケづつ保存し、1ケ月に3ケづつ任意に取り出
し包装を破り、内側のアルミの腐蝕を観察した。
結果を表1に示す。[Table] Compress 3g of each of the five mixtures A to E having the above composition into tablets, seal them in aluminum pillow packaging, and store them in a constant temperature room at 20℃ for 6 months. Corrosion was observed. each sample
I stored 30 pieces at a time, and took out 3 pieces every month at will, tore the packaging, and observed the corrosion of the aluminum inside.
The results are shown in Table 1.
【表】 実施施例 2【table】 Implementation example 2
【表】
A型ゼオライトを種々の水分含量に調整して上
記配合組成を有する組成物を作り3g量づつアル
ミピロ包装に密閉しし6ケ月保存した。実施例1
と同様にアルミ面に生じる腐蝕を観察した。
結果を表2に示す。[Table] A-type zeolite was adjusted to various moisture contents to prepare compositions having the above compositions, which were sealed in aluminum pyropackaging in 3 g portions and stored for 6 months. Example 1
Corrosion occurring on the aluminum surface was observed in the same manner. The results are shown in Table 2.
【表】 実施例 3【table】 Example 3
【表】
上記組成を有するH〜Kの4種の混合物を1錠
30gの量で3ケ打錠し、扁平円柱状の錠剤をつく
つた。これを500c.c.広口ポリエチレンボトルに密
栓して保存した。6ケ月室温保存後に開詮した。
Hは強い塩素の刺激臭があつたがI〜Kはほとん
ど塩素臭はなかつた。
実施例 4[Table] 1 tablet of a mixture of 4 types of H to K having the above composition
Three 30g tablets were compressed to produce flat cylindrical tablets. This was stored in a 500 c.c. wide-mouth polyethylene bottle with a tightly stopper. It was opened after being stored at room temperature for 6 months.
H had a strong pungent odor of chlorine, but I to K had almost no chlorine odor. Example 4
【表】
上記の表に示した組成を有するL〜Qの6種の
混合物を夫々3gずつ錠剤に打錠し、アルミピロ
包装に密封して、40℃の恒温室に保存し、ピロ包
装のアルミ面に生ずる腐蝕を観察した。夫々サン
プルを9ケずつ保存し、15日後、30日後、45日後
に3ケずつ任意に取り出し包装を破り、内側のア
ルミの腐蝕を観察した。その結果を上記の表に併
せて示した。
この加速試験は、40℃、45日で20℃、6ケ月の
試験にほぼ相応する。
上表より、合成非晶質ゼオライトを使用した場
合は分解抑止効果はあるが、多量に配合する必要
があるのに対し、本発明で使用する合成結晶型A
型ゼオライトは少量で効果があることがわかる。
また、合成非晶質ゼオライトを使用した場合、打
錠性がよくなかつた。即ち、ある程度の分解抑止
効果を示す組成物O,Pを打錠した錠剤は脆く手
でくだけやすかつた。[Table] The six mixtures L to Q having the compositions shown in the table above were compressed into tablets of 3 g each, sealed in aluminum pyro packaging, stored in a constant temperature room at 40°C, and placed in aluminum pyro packaging. Corrosion occurring on the surface was observed. Nine samples of each were stored, and after 15, 30, and 45 days, three samples were taken out at will, the packaging was torn, and the corrosion of the aluminum inside was observed. The results are also shown in the table above. This accelerated test is approximately equivalent to a 6-month test at 20°C for 45 days at 40°C. From the table above, it can be seen that when synthetic amorphous zeolite is used, it has the effect of suppressing decomposition, but it needs to be blended in a large amount, whereas synthetic crystal type A used in the present invention
It can be seen that zeolite type is effective in small amounts.
Furthermore, when synthetic amorphous zeolite was used, tableting properties were not good. That is, the tablets obtained by compressing compositions O and P, which exhibit a certain degree of decomposition-inhibiting effect, were brittle and easy to break apart by hand.
Claims (1)
ロルイソシアヌール酸カリウム及びジクロルイソ
シアヌール酸からなる群から選ばれた1種又は2
種以上の粉末塩素系漂白剤と、含成結晶型A型ゼ
オライトとを重量比で97/3〜70/30の割合で含
有することを特徴とする粉末塩素系漂白剤の安定
化組成物。 2 A型ゼオライトの水分含量が実質的に0であ
る特許請求の範囲第1項記載の組成物。[Claims] 1. One or two selected from the group consisting of sodium dichloroisocyanurate, potassium dichloroisocyanurate, and dichloroisocyanuric acid.
1. A stabilized composition for a powdered chlorine bleach, comprising at least one powdered chlorine bleach and a crystal type A zeolite in a weight ratio of 97/3 to 70/30. 2. The composition according to claim 1, wherein the water content of the A-type zeolite is substantially zero.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19971281A JPS58101199A (en) | 1981-12-11 | 1981-12-11 | Stabilizing composition for powder chlorine bleaching agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19971281A JPS58101199A (en) | 1981-12-11 | 1981-12-11 | Stabilizing composition for powder chlorine bleaching agent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58101199A JPS58101199A (en) | 1983-06-16 |
JPH0335359B2 true JPH0335359B2 (en) | 1991-05-27 |
Family
ID=16412350
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19971281A Granted JPS58101199A (en) | 1981-12-11 | 1981-12-11 | Stabilizing composition for powder chlorine bleaching agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58101199A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4389325A (en) * | 1982-01-25 | 1983-06-21 | Monsanto Company | Chloroisocyanurate compositions |
JPS61145169A (en) * | 1984-12-18 | 1986-07-02 | Nissan Chem Ind Ltd | Storage of solid chlorination agent |
JPS6225198A (en) * | 1985-07-25 | 1987-02-03 | ユ−ホ−ケミカル株式会社 | Bleaching detergent composition |
FR2658194B1 (en) * | 1990-02-15 | 1994-05-20 | Norsolor Sa | PROCESS FOR STORING CHLOROISOCYANURATES. |
JP4708776B2 (en) * | 2004-12-10 | 2011-06-22 | エステー株式会社 | Solid drain pipe cleaning agent and drain pipe cleaning method |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5197608A (en) * | 1975-01-24 | 1976-08-27 |
-
1981
- 1981-12-11 JP JP19971281A patent/JPS58101199A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5197608A (en) * | 1975-01-24 | 1976-08-27 |
Also Published As
Publication number | Publication date |
---|---|
JPS58101199A (en) | 1983-06-16 |
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