JPS5811033A - Coagulation preventing agent for neutral inorganic salts - Google Patents

Coagulation preventing agent for neutral inorganic salts

Info

Publication number
JPS5811033A
JPS5811033A JP10944781A JP10944781A JPS5811033A JP S5811033 A JPS5811033 A JP S5811033A JP 10944781 A JP10944781 A JP 10944781A JP 10944781 A JP10944781 A JP 10944781A JP S5811033 A JPS5811033 A JP S5811033A
Authority
JP
Japan
Prior art keywords
salts
coagulation
agents
neutral
preventing agent
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
JP10944781A
Other languages
Japanese (ja)
Other versions
JPH0153096B2 (en
Inventor
Minoru Nishi
実 西
Kenichi Oikawa
健一 及川
Kinji Kaneda
金田 勤治
Shinsuke Fujita
晋介 藤田
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.)
Sogo Pharmaceutical Co Ltd
Original Assignee
Sogo Pharmaceutical 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 Sogo Pharmaceutical Co Ltd filed Critical Sogo Pharmaceutical Co Ltd
Priority to JP10944781A priority Critical patent/JPS5811033A/en
Publication of JPS5811033A publication Critical patent/JPS5811033A/en
Publication of JPH0153096B2 publication Critical patent/JPH0153096B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To prevent the coagulation of neutral inorg. salts effectively by combining >=2 kinds of moisture absorbing and deliquescing agents of different properties as a coagulation preventing agent for said salts. CONSTITUTION:The agents prepd. by adding and compounding >=2 kinds of moisture absorbing and deliquescing agents such as ammonium iron citrate, neopentyl glycol and the like which differ in moisture absorption time, coagulation time, etc. are used for a coagulation preventing agent for neutral inorg. salts such as rock salt, calciun chloride and the like. Then the migration of water between the moisture absorbing agents and the deliquescing agents takes place and the coagulation of the neutral inorg. salts is prevented extremely effectively.

Description

【発明の詳細な説明】 本発明は、各種の中性無機塩類が凝結するのを防止する
凝結防止剤に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an anti-caking agent that prevents various neutral inorganic salts from coagulating.

中性無機塩角は、純粋な物質であってもその表面に自由
水、吸湿水等各種の水分を保有しており、放置しておく
とこれらの水分が結合剤となって凝結現象が生じる。こ
の傾向は、中性無機塩類が未精製のものであって不純物
(特にカルシウム塩、マグネシウム塩)を含有する場合
には特に著しい。
Neutral inorganic salt cubes, even if they are pure substances, contain various kinds of moisture such as free water and hygroscopic water on their surfaces, and if left undisturbed, these moistures will act as a binder and cause a condensation phenomenon. . This tendency is particularly remarkable when the neutral inorganic salt is unrefined and contains impurities (particularly calcium salts and magnesium salts).

例えば、塩化カリウム、苛性カリ、炭酸カリウムの製造
原料であると同時に冬期における氷結道路上のすべり止
め材としてもしばしば利用される岩塩であって、特に加
工されていない岩塩を例にとるまでもなく、中性無機塩
角は、粉砕されたままで袋につめられるものには、その
表面に自由水や吸湿水を持っている。これ等、水分が極
自然に結合剤となり、袋のつみ重ねにより凝結現象を引
き起こす。さらに、これ等塩類の凝固には、粒度分布や
紋型が影響して最密充填の状態になったならば塩類の凝
結度は数百に9 / cm2をも示す様になり取扱いが
非常に不便な固まりとなシ作業性は著しく低下する。た
とえば水分含量が04%の岩塩の袋1000kgを放置
しておくと、日数が長くなればなるほど凝結が促進され
る。この岩塩を、袋から取り出し処理装置のホッパーに
投入してもホッパー内でブリッジ現象を生じてしまうこ
とは良く知られている。
For example, rock salt, which is often used as a raw material for the production of potassium chloride, caustic potash, and potassium carbonate, and also as a non-slip material on frozen roads in winter, need not be taken as an example of unprocessed rock salt. Neutral inorganic salt cubes that are crushed and packed in bags have free water or hygroscopic water on their surface. In these cases, water naturally acts as a binder, causing condensation when the bags are piled up. Furthermore, the coagulation of these salts is affected by the particle size distribution and pattern, and if they reach a close-packed state, the degree of coagulation of the salts will be in the hundreds to 9/cm2, making them extremely difficult to handle. Workability is significantly reduced due to inconvenient lumps. For example, if you leave a 1,000 kg bag of rock salt with a moisture content of 0.4% undisturbed, the longer the days, the more it will solidify. It is well known that even if this rock salt is taken out of the bag and put into the hopper of a processing device, a bridging phenomenon occurs in the hopper.

つまり、無機工業薬品の製造原料又は反応試栗としての
中性無機塩類(例えば岩塩、食塩、塩化カルシウム、塩
化マグネシウム)が凝結してしまったのでは、これを再
度粉砕しなければならず、無機工業薬品の製造プラント
での取扱いに多大の労力を費し、コスト高を招来する。
In other words, if neutral inorganic salts (e.g., rock salt, common salt, calcium chloride, magnesium chloride) used as raw materials for manufacturing inorganic industrial chemicals or reaction test chestnuts have condensed, they must be crushed again, and the inorganic It takes a lot of effort to handle industrial chemicals at a manufacturing plant, leading to high costs.

また、特に食塩、塩カル、塩マグのように、これを冬期
の氷結した道路路面上に散布して路面上の氷雪をとかす
ため、これらの塩類をマテリアルスプレッダ−等で散布
する場合、これらの塩類が凝固したのでは散布作業はた
ちまち停止せざるを得なくなる。特にこれら散布作業は
降雪時の戸外で行うことが多いため、戸外の水分の影響
をまともに受け、その結果塩類の凝固、凝結がますます
促進されるので、これを防止する手段が当業界において
とりわけ切望されていた。
In addition, when these salts, such as table salt, salt calcined salt, and salt mugs, are spread on frozen roads in winter to melt ice and snow on the road surface, when these salts are spread with a material spreader, etc. If the salt solidifies, the spraying operation will have to stop immediately. In particular, since these spraying operations are often carried out outdoors during snowfall, they are exposed to the influence of outdoor moisture, which further accelerates the coagulation and condensation of salts. It was especially coveted.

本発明は、このような業界の要望にこれえ、中性無機塩
類の凝結を阻止する手段を開発するためになされたもの
である。この目的達成のために本発明者は鋭意研寵を重
ねた結果、吸湿時間、固結時間等性質の異なる吸湿潮解
剤を2種以上中性熱(3) 機塩類に添力ロ配合すれば該塩類の凝固が極めて有効に
防止されることを発見し、この新知見を基礎にして更に
研究をすすめて本発明を完成した。
The present invention was made in order to meet the needs of the industry and to develop a means for preventing the condensation of neutral inorganic salts. In order to achieve this objective, the inventor of the present invention made extensive research and found that it is possible to mix two or more types of hygroscopic deliquescent agents with different properties such as moisture absorption time and consolidation time with neutral heat (3) machine salts. It was discovered that coagulation of the salts was extremely effectively prevented, and based on this new knowledge, further research was conducted and the present invention was completed.

そのメカニズムの詳ituは不明であるが、吸湿潮解剤
は、水分飽和に達する時間の違いや、飽和に達した後の
条件たとえば温度、湿度圧力によってそれぞれ異なった
状態になり、従って、これ等を混合するとたえず吸湿剤
潮解剤相互間で水分の移動が行なわれ、この原理を応用
して中性無機塩類の凝固が防止されるものと推測される
Although the details of the mechanism are unknown, hygroscopic deliquescent agents enter different states depending on the time it takes to reach water saturation and the conditions after reaching saturation, such as temperature and humidity pressure. When mixed, moisture constantly moves between the moisture absorbent and the deliquescent agent, and it is presumed that this principle is applied to prevent the neutral inorganic salts from coagulating.

本発明において使用される吸湿潮解剤は、吸湿性、吸着
性及び/又は潮解性を有する物質であって、中性無機塩
類と反応したり又はこれらに悪影響を与えないものであ
ればすべての物が適宜使用される。その例としては、例
えば、シリカゲル、硫酸塩(例えば、硫酸アルミニウム
)、クエン酸鉄アンモニウム、塩化コリン、酒石酸水素
コリン、コリンのクエン酸二水素塩、コリンのグルコン
酸塩、グリコール(例えばネオペンチルグリコール等ア
ルキルグリコール;エチレンクリコール、)(4) ロピレングリコール、トリメチレングリコール、1.4
−ブタンジオール、1.5−はンタンジオール等アルキ
レンクリコール;シクロペンタン1゜2−ジオール、シ
クロヘキサン1.2−:)オール等シクロアルキルジオ
ール)、活性炭、木炭その他が挙げられるが、これのみ
に限定されるものではない。これらの吸湿潮解剤は、単
独で使用したのでは所期の目的は達成されず、吸湿時間
、固結時間等性質の異なる物を2種以上併用することが
必要である。
The hygroscopic deliquescent agent used in the present invention is any substance that has hygroscopic, adsorbent and/or deliquescent properties, and does not react with or adversely affect neutral inorganic salts. is used as appropriate. Examples include, for example, silica gel, sulfates (e.g. aluminum sulfate), ferrous ammonium citrate, choline chloride, choline bitartrate, choline dihydrogen citrate, choline gluconate, glycols (e.g. neopentyl glycol). Equal alkyl glycol; ethylene glycol, ) (4) Ropylene glycol, trimethylene glycol, 1.4
Alkylene glycols such as -butanediol, 1.5-butanediol; cycloalkyl diols such as cyclopentane 1゜2-diol, cyclohexane 1.2-:)ol, activated carbon, charcoal, etc. It is not limited. If these hygroscopic deliquescent agents are used alone, the intended purpose cannot be achieved, and it is necessary to use two or more of them having different properties such as moisture absorption time and solidification time.

上記吸湿剤潮解剤は、これのみを凝固防止剤として塩類
に添加しても充分に所期の目的が達成されるが、界面活
性剤で更に処理すれば一層すぐれた効果が奏される。こ
の処理は、これを吸湿剤に配合、混合したり、被覆処理
して行う。そのメカニズムの詳細は今後の研究に一層た
ねばならないが、吸湿剤潮解剤が吸湿した結果界面活性
剤が表面に浸出して、被膜を中性無機塩類に形成し、こ
の現象がさらに凝結防止の効果を強力にするものと推定
される。
The desiccant deliquescent agent described above can sufficiently achieve the intended purpose when added alone to salts as an anti-caking agent, but an even better effect can be achieved if it is further treated with a surfactant. This treatment is carried out by blending it with a moisture absorbent, mixing it, or coating it. The details of this mechanism will require further research, but as a result of moisture absorption by the desiccant deliquescent agent, the surfactant leaches out to the surface, forming a film of neutral inorganic salts, and this phenomenon further prevents caking. It is estimated that the effect will be stronger.

界面活性剤としては、合成、天然を問わず、各種の陰イ
オン系、陽イオン系、両性系及び非イオン系の界面活性
剤が広く使用できるが、特に天然油脂系界面活性剤は好
適である。その例としては、高級脂肪酸アルカリ塩、ア
ルキル硫酸塩(アルキルサルフェート)、アルコールサ
ルフェート(例えば、サンノールLPF、LL−103
)、ポリエチレングリコールリ旨肋酸エステル、ソルビ
タン脂肪酸エステル、脂肪酸モノグリセリド等が挙げら
れる。
As the surfactant, various anionic, cationic, amphoteric, and nonionic surfactants, whether synthetic or natural, can be widely used, but natural oil-based surfactants are particularly suitable. . Examples include higher fatty acid alkali salts, alkyl sulfates, alcohol sulfates (e.g. Sannol LPF, LL-103
), polyethylene glycol fatty acid ester, sorbitan fatty acid ester, fatty acid monoglyceride, and the like.

本発明に係る凝固防止剤は、すべての中性無機塩類、例
えば岩塩、食塩、塩化カルシウム、塩化マグネシウム、
塩化アンモニウム、硝酸ナトリウム、硫酸ナトリウム等
に対して広く適用することができる。
The anticaking agent according to the present invention includes all neutral inorganic salts, such as rock salt, common salt, calcium chloride, magnesium chloride,
It can be widely applied to ammonium chloride, sodium nitrate, sodium sulfate, etc.

本発明によれば、冬期における道路路面の氷雪を除去す
るために袋から取り出してマテリアルスプレッダ−等に
投入して塩カリ、塩マグ、食塩、岩塩等を散布する際、
湿度の高い劣悪な気象条件のためとわら中性無機塩類を
マテリアルスゾレツグーに投入する作業工程とマテリア
ルスゾレツダー内で固結してし壕うことが非常に多くあ
h人手が掛かったり機械が停止してしまうことがしばし
ばであるが、このようなことがなくなり、散布作業が円
滑に実施できる。この場合の塩類の散布量は、積雪の紫
によっても異なるが、5園程度の積雪の場合は3朋程度
の粒状のものを約40y−/m2程度が適当であるが、
本発明によれば塩類が凝固しないために、上記散布間を
常に維持することができるほか、必要に応じて散布量を
適宜自由にコントロールすることができ、しかも均一・
に散布することができる。また、無機化学Tv、肥料工
業等において、これら塩類を原料その他として使用する
場合、プラントのパイプ、反応タンク内で凝固すること
がなく、反応がスムースに行われるし、ホツノt−内で
のブリッジング、ラットホーリングといった好ましくな
い現象も防止することができる。そのうえ、これら塩類
(d、いくら防湿1生の袋に入れて貯蔵しても、貯TW
、J04間が長くな:FLは袋の中でどうしても固結す
るものであるけれども、本(7) 発明によればそれが防止されるという著効も得られる。
According to the present invention, when removing ice and snow from a road surface in winter by removing it from a bag and putting it into a material spreader or the like to spread salt potash, salt mug, table salt, rock salt, etc.,
Due to the high humidity and poor weather conditions, the work process of adding neutral inorganic salts to the material sludge and the process of adding them to the material sludge often require a lot of manual labor. The machine often stops, but this is no longer the case, and the spraying work can be carried out smoothly. The amount of salt to be sprayed in this case will vary depending on the purple color of the snow, but in the case of snow covering about 5 gardens, it is appropriate to spray about 40 y-/m2 of granular salts of about 3 square meters.
According to the present invention, since the salts do not coagulate, the above-mentioned spraying interval can be maintained at all times, and the spraying amount can be freely controlled as needed, and the spraying rate can be uniform and uniform.
can be dispersed. In addition, when these salts are used as raw materials or other materials in the inorganic chemistry industry, fertilizer industry, etc., they do not coagulate in plant pipes or reaction tanks, and reactions occur smoothly. Undesirable phenomena such as ringing and ratholing can also be prevented. Moreover, even if these salts (d) are stored in moisture-proof bags, the storage capacity is
, J04 is long: FL inevitably solidifies in the bag, but the present invention (7) has the remarkable effect of preventing this from happening.

実施例1゜ それぞれ重量でクエン酸鉄アンモニウム14′5部、ネ
オペンチルグリコール628物を混合し、6部の水に溶
かしたアルコールサルフェート25.9部で被覆する。
Example 1: 14'5 parts by weight of ferrous ammonium citrate and 628 parts of neopentyl glycol are mixed and coated with 25.9 parts of alcohol sulfate dissolved in 6 parts of water.

そして、乾燥、脱水して、粉砕して、80〜150メツ
シユの粉状凝結防止剤を得る。
Then, it is dried, dehydrated, and pulverized to obtain a powdery anti-caking agent of 80 to 150 mesh.

ここに得ら:hだ凝固防止剤を1部取り、04%〜4%
の含水中間粉砕食tg I CI O0部にミキサー内
で攪拌混合17たものを約85y−取り、40#l/c
In2の土性で35φ×75〜80の円柱に成型j〜だ
Here you get: Take 1 part of anti-caking agent, 0.4%~4%
About 85y of 0 parts of water-containing intermediate pulverized food tg I CI O was stirred and mixed in a mixer, and 40#l/c
It is molded into a cylinder of 35φ x 75~80 mm with the soil quality of In2.

比較品は先の04%〜4%の食塩を用いて成郊したもの
を用意した。脱7g後0時間、24時間、2週間経過1
.た時の破壊強度は以下の様であった。
Comparative products were prepared using 4% to 4% salt. 0 hours, 24 hours, and 2 weeks after withdrawal of 7g 1
.. The breaking strength was as follows.

(8) 表−1 実施例2゜ 食塩の代わりに塩化マグネシウム、6水塩ヲ1000部
使用し7て実施例1と同様に処理して凝固防止剤を得た
。これは、実施例1と同様のすぐれた結果を示したが、
更に凝結防止剤の使用量は減少する方向にあつ′fC6 実施例6 それぞれ重量でり王ン酸鉄マンモニウム333部、硫、
酸アルミニウムか6.6部を混合し、6部の水に溶かし
たアルコールサルフエ−1・60部で被接[7て得られ
た凝固防止剤の粉体は、実施例1と同様なすぐれた結果
を示した。
(8) Table 1 Example 2 An anti-caking agent was obtained in the same manner as in Example 1 except that 1000 parts of magnesium chloride and hexahydrate were used instead of common salt. This showed excellent results similar to Example 1, but
Furthermore, the amount of anti-caking agents used is decreasing.
6.6 parts of aluminum acid was mixed and coated with 1.60 parts of alcohol sulfur dissolved in 6 parts of water. The results were shown.

代理人 弁理士  戸 1)親 男Agent Patent Attorney 1) Parent Male

Claims (1)

【特許請求の範囲】 1、 性質の異なる2種以上の吸湿潮解剤からなること
を特徴とする中性無機塩類の凝結防止剤。 2、該吸湿潮解剤を界面活性剤で処理したことを特徴と
する特許請求の範囲第1項に記載の凝結防止剤。 6、該界面活性剤が天然油脂系界面活性剤であることを
特徴とする特許請求の範囲第2項に記載の凝結防止剤。
[Scope of Claims] 1. An anti-caking agent of neutral inorganic salts, characterized by comprising two or more types of hygroscopic deliquescent agents having different properties. 2. The anti-caking agent according to claim 1, wherein the moisture-absorbing deliquescent agent is treated with a surfactant. 6. The anti-caking agent according to claim 2, wherein the surfactant is a natural oil-based surfactant.
JP10944781A 1981-07-15 1981-07-15 Coagulation preventing agent for neutral inorganic salts Granted JPS5811033A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10944781A JPS5811033A (en) 1981-07-15 1981-07-15 Coagulation preventing agent for neutral inorganic salts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10944781A JPS5811033A (en) 1981-07-15 1981-07-15 Coagulation preventing agent for neutral inorganic salts

Publications (2)

Publication Number Publication Date
JPS5811033A true JPS5811033A (en) 1983-01-21
JPH0153096B2 JPH0153096B2 (en) 1989-11-13

Family

ID=14510464

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10944781A Granted JPS5811033A (en) 1981-07-15 1981-07-15 Coagulation preventing agent for neutral inorganic salts

Country Status (1)

Country Link
JP (1) JPS5811033A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61291415A (en) * 1985-06-18 1986-12-22 Mitsubishi Metal Corp Easily dispersible calcium chloride containing silicic acid and production thereof
US6093336A (en) * 1996-05-31 2000-07-25 Akzo Nobel Nv Process for making solid compositions comprising quaternary ester ammonium compounds and fatty acids
US6613405B1 (en) * 1995-04-19 2003-09-02 Csp Technologies, Inc. Monolithic composition having the capability of maintaining constant relative humidity in a package

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61291415A (en) * 1985-06-18 1986-12-22 Mitsubishi Metal Corp Easily dispersible calcium chloride containing silicic acid and production thereof
JPH032804B2 (en) * 1985-06-18 1991-01-17 Mitsubishi Materiaru Kk
US6613405B1 (en) * 1995-04-19 2003-09-02 Csp Technologies, Inc. Monolithic composition having the capability of maintaining constant relative humidity in a package
US6093336A (en) * 1996-05-31 2000-07-25 Akzo Nobel Nv Process for making solid compositions comprising quaternary ester ammonium compounds and fatty acids

Also Published As

Publication number Publication date
JPH0153096B2 (en) 1989-11-13

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