JPH01278593A - Strongly basic solution and solid strong base - Google Patents
Strongly basic solution and solid strong baseInfo
- Publication number
- JPH01278593A JPH01278593A JP10680188A JP10680188A JPH01278593A JP H01278593 A JPH01278593 A JP H01278593A JP 10680188 A JP10680188 A JP 10680188A JP 10680188 A JP10680188 A JP 10680188A JP H01278593 A JPH01278593 A JP H01278593A
- Authority
- JP
- Japan
- Prior art keywords
- solution
- precipitate
- aqueous solution
- strong
- seawater
- 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
Links
- 239000002585 base Substances 0.000 title claims abstract description 20
- 239000003637 basic solution Substances 0.000 title claims abstract description 15
- 239000007787 solid Substances 0.000 title claims abstract description 15
- 239000013535 sea water Substances 0.000 claims abstract description 30
- 239000000243 solution Substances 0.000 claims abstract description 25
- 239000002244 precipitate Substances 0.000 claims abstract description 22
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 238000001816 cooling Methods 0.000 claims abstract description 6
- 230000002378 acidificating effect Effects 0.000 claims description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 27
- 239000007864 aqueous solution Substances 0.000 abstract description 17
- 239000002253 acid Substances 0.000 abstract description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 10
- 239000007788 liquid Substances 0.000 abstract description 7
- 239000002904 solvent Substances 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 6
- 238000004140 cleaning Methods 0.000 abstract description 4
- 230000003472 neutralizing effect Effects 0.000 abstract description 3
- 239000003054 catalyst Substances 0.000 abstract description 2
- 239000011248 coating agent Substances 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 abstract description 2
- 239000003607 modifier Substances 0.000 abstract description 2
- 239000010865 sewage Substances 0.000 abstract description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical class [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 abstract description 2
- 239000006228 supernatant Substances 0.000 abstract 3
- 239000012530 fluid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000011734 sodium Substances 0.000 description 8
- 239000003973 paint Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- TXKUEILVFFGAIG-UHFFFAOYSA-K [OH-].[OH-].[OH-].[Na+].[Na+].[Na+] Chemical compound [OH-].[OH-].[OH-].[Na+].[Na+].[Na+] TXKUEILVFFGAIG-UHFFFAOYSA-K 0.000 description 2
- 229910001413 alkali metal ion Inorganic materials 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 229910001416 lithium ion Inorganic materials 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- 230000005856 abnormality Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- -1 hydroxide ions Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- SFKTYEXKZXBQRQ-UHFFFAOYSA-J thorium(4+);tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Th+4] SFKTYEXKZXBQRQ-UHFFFAOYSA-J 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
この発明は、水酸化すI〜リウ八への従来アルカリに代
わる強塩基性の物質に係わり、各種洗浄液、中和剤、汚
水処理剤、触媒として用いられる他、塗料用溶剤として
更にはガソリン等の改質剤として適用することのできる
極めて塩基性の強い物質に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a strong basic substance that replaces conventional alkalis for hydroxides I to R-8, and is suitable for use in various cleaning solutions, neutralizing agents, sewage treatment agents, The present invention relates to an extremely basic substance that can be used as a catalyst, a paint solvent, and a modifier for gasoline, etc.
[従来の技術及び発明が解決しようとする課題]従来よ
り各種工業において洗浄液、中和剤等どして主として水
酸化ナトリウム及びその水溶液が用いられている。[Prior Art and Problems to be Solved by the Invention] Conventionally, sodium hydroxide and its aqueous solution have been mainly used as cleaning liquids, neutralizing agents, etc. in various industries.
しかし、水酸化ナトリウムは潮解性が大きいために扱い
にくく、又、その水溶液は粘性があるため塗料の溶剤等
用途によっては適用することができない。However, sodium hydroxide is difficult to handle because of its large deliquescent property, and its aqueous solution is viscous, so it cannot be used as a solvent for paints or other applications.
ところで、近年、アルカリ土類酸化物等の特定の金属酸
化物にNa金属を添加したものが極めて強い塩基性を示
し、触媒作用等に興味ある挙動を示すことが報告されて
いる。このような極めて強い塩基性を示す物質は超強塩
基と呼ばれ(その定義は不明確であるが)、現在のとこ
ろMgOにNaを添加したNa−MgO、AQ、03に
Na金属を添加したNa−A、Q、03、CaOを真空
中で焼成したものなどが知られている。Incidentally, in recent years, it has been reported that certain metal oxides such as alkaline earth oxides to which Na metal is added exhibit extremely strong basicity and exhibit interesting behavior in terms of catalysis and the like. Substances that exhibit extremely strong basicity are called superstrong bases (although the definition is unclear), and currently there are three types: Na-MgO, which is MgO with Na added, AQ, and 03 with Na metal added. Those obtained by firing Na-A, Q, 03, and CaO in a vacuum are known.
これらの物質は特に有機合成化学上重要性が着用されて
いるが、その物理化学的性質等が研究途上であり、また
空気中ではない特定条件下(例えばアルゴン中とか真空
中など)で焼成する、Na金属を必要とするなど製造」
二の困難性から未だ工業的に実用化されていないし、ま
たアルカリ剤が大量に使用される分野には適していない
。These substances are particularly important in terms of organic synthesis chemistry, but their physicochemical properties are still under research, and they must be fired under specific conditions other than in air (for example, in argon or vacuum). , Manufacture that requires Na metal, etc.
Due to the second difficulty, it has not yet been put into practical use industrially, and it is not suitable for fields where a large amount of alkaline agents are used.
この発明は、安価かつ、容易に量産でき、種々の用途に
用いることのできる強塩基を提供することを目的とする
。The object of the present invention is to provide a strong base that is inexpensive, can be easily mass-produced, and can be used for various purposes.
更にこの発明は、海水を利用して製造される水酸化ナト
リウムに代わる強塩基性溶液及び固体強塩基を提供する
ことを目的とする。A further object of the present invention is to provide a strong basic solution and solid strong base that can replace sodium hydroxide produced using seawater.
[課題を解決するための手段]
このような目的を達成する本発明の強塩基の一つは、海
水を酸性にした後、強アルカリ剤を加え高p I−1に
しその際生成する沈澱物を除去して得られた溶液(、)
を濃縮後、冷却し、冷却の際生成する沈澱物を除去する
ことによって得られる溶液(b)であり、他の一つは溶
液(b)から水分を除去することによって得られる固体
である。[Means for Solving the Problems] One of the strong bases of the present invention that achieves this purpose is to make seawater acidic, then add a strong alkaline agent to make it have a high p I-1, and remove the precipitate generated at that time. Solution obtained by removing (,)
Solution (b) is obtained by concentrating, cooling, and removing the precipitate generated during cooling, and the other is a solid obtained by removing water from solution (b).
本発明者はすでに提案した「海水の塩分離方法」(特願
昭62−201578号)において、海水を硫酸イオン
を含有する強酸により低pHに調整した後、強アルカリ
剤を加え高pHにしその際生成する沈澱物と溶液(a)
とを分離することにより、海水中に含まれる各種金属イ
オン等のイオンを分離しうろことを示した。本発明の強
塩基はこの溶液(a)を基礎として製造される。The present inventor has already proposed a method for separating salts from seawater (Japanese Patent Application No. 62-201578), in which the pH of seawater is adjusted to low with a strong acid containing sulfate ions, and then a strong alkaline agent is added to raise the pH to high. Precipitate and solution (a)
It was shown that ions such as various metal ions contained in seawater can be separated and scaled by separating them. The strong bases of the invention are prepared on the basis of this solution (a).
以下、海水の分離について簡単に説明する。まず海水を
低pHにするための硫酸イオンを含有する強酸としては
、数%の希硫酸を用いることができるが、活性化した燐
酸力ルシウl\を溶解せしめた水溶液に3〜5%の濃硫
酸を加えて沈澱物を除去した水溶液(以下P−8酸と略
す)を用いることができる。このP−8酸は、pI(0
,2程度の強酸性を示すが硫酸のような劇物とは異なり
肌に触れても異常がなく扱いやすい安全性の高い酸とし
て利用できる。希硫酸あるいはP −S酸を海水に対し
数%加え、2〜3時間放置することにより海水をpH2
以下の低p、 Hに調整することかできる。Seawater separation will be briefly explained below. First, a few percent dilute sulfuric acid can be used as a strong acid containing sulfate ions to lower the pH of seawater, but 3 to 5 percent concentrated acid can be used in an aqueous solution in which activated phosphoric acid is dissolved. An aqueous solution (hereinafter abbreviated as P-8 acid) obtained by adding sulfuric acid and removing a precipitate can be used. This P-8 acid has a pI (0
It exhibits a strong acidity of about .2, but unlike harmful substances such as sulfuric acid, it can be used as a highly safe acid that is easy to handle and does not cause any abnormality when it comes in contact with the skin. Add a few percent of dilute sulfuric acid or P-S acid to seawater and leave it for 2 to 3 hours to adjust the pH of the seawater to 2.
It is possible to adjust to the following low p and H values.
この時、沈澱物は殆ど生しないが若干の沈澱物はもとの
海水中の懸濁物質と共に濾過等の手段により除去する。At this time, almost no precipitates are formed, but some precipitates are removed together with the original suspended matter in the seawater by means such as filtration.
次に、強アルカリ剤は、−度低pHに調整した海水を中
和し、更に高pHにするためのもので、これにより高p
Hで溶解度の低下するアルカリ上金属類、その他金属の
硫酸塩等の塩類を沈澱せしめる。このような強アルカリ
剤としては、水酸化ナトリウムをそのまま、あるいは酸
化カルシウムの水溶液に水酸化ナトリウムを加えたもの
(以下、Ca−Na水溶液と略す)などが用いられる。Next, the strong alkaline agent is used to neutralize seawater that has been adjusted to a low pH and raise the pH further.
Hydrogen precipitates alkali metals whose solubility decreases and salts such as sulfates of other metals. As such a strong alkaline agent, sodium hydroxide as it is, or a solution obtained by adding sodium hydroxide to an aqueous solution of calcium oxide (hereinafter abbreviated as Ca--Na aqueous solution) is used.
強アルカリ剤の量は上記目的を達成することのできる量
以上であればよく、通常水酸化すトリウム(固体)の場
合海水に対し3%、Ca−Naの水溶液の場合約5%加
え、10時間以上放置する。The amount of strong alkaline agent should be at least the amount that can achieve the above purpose, and usually 3% of thorium hydroxide (solid) is added to seawater, and about 5% of Ca-Na aqueous solution is added to 10% of the seawater. Leave it for more than an hour.
これによって海水はp、H13以上の塩基性を呈し、沈
澱物が生成する。As a result, the seawater exhibits a basicity of p, H13 or more, and a precipitate is formed.
この沈澱物を除去後の溶液(a)は、海水に比へアルカ
リ金属イオンは同程度であるが、Ca、Mg等のアルカ
リ士金属イオンが少なく、また陰イオンとして主として
水酸イオン及び塩素イオン登含有する塩基性の水溶液で
ある。After removing this precipitate, solution (a) contains about the same amount of alkali metal ions as seawater, but contains less alkali metal ions such as Ca and Mg, and contains mainly hydroxide ions and chloride ions as anions. It is a basic aqueous solution containing
次に、このようにして海水を分離して得られた溶液(a
)から本発明の強塩基を製造する方法[3ついて説明す
る。Next, the solution obtained by separating seawater in this way (a
) to produce the strong base of the present invention [3] will be explained.
ます、溶液(a)を加熱して水分を蒸発させることによ
り適当に濃縮する。この濃縮したものを冷却すると沈澱
物が析出するので、この沈澱物を除去することにより極
めて塩基性の強い溶液(b)を得る。First, solution (a) is appropriately concentrated by heating to evaporate water. When this concentrated product is cooled, a precipitate is deposited, and by removing this precipitate, a very strongly basic solution (b) is obtained.
ここで濃縮の度合は溶液(b)を適用する目的によって
異なるが、元の溶液(a)の1割〜1.5割程度まで濃
縮することによりp H14を越える極めて強い塩基性
溶液を得ることができる。最初に海水を分離して得られ
た溶液(a)、溶液(b)及び海水の元素分析の結果を
表1に示す。The degree of concentration here varies depending on the purpose for which solution (b) is applied, but by concentrating it to about 10% to 1.50% of the original solution (a), an extremely strong basic solution with a pH exceeding 14 can be obtained. I can do it. Table 1 shows the results of elemental analysis of solutions (a) and (b) obtained by first separating seawater and the seawater.
この7容液(b)は最初に海水を分離して得られた溶液
(a)から更に解離度の低い塩を沈澱物として除去した
ものであるので、陽イオンとしてNa+、K+、Ca+
+を主として含み海水に比べLi+イオンが多く含まれ
る。This 7-volume solution (b) is obtained by removing salts with a lower degree of dissociation as precipitates from the solution (a) obtained by first separating seawater, so it contains Na+, K+, Ca+ as cations.
It mainly contains Li+ ions, and contains more Li+ ions than seawater.
このような塩基性溶液は、水酸化すI〜リウム水溶液の
代用として洗浄液、中和剤に有効に使用することができ
るが、船のエンジンの周囲に生じる海水と重油等の混合
汚水を処理し、海水と油を分離する分離剤として、また
製紙工場等から排出される酸性廃液の処理液としても優
れた効果を発揮する。Such basic solutions can be effectively used as cleaning solutions and neutralizers as substitutes for aqueous solutions of sodium to lithium hydroxide; It exhibits excellent effects as a separating agent for separating seawater and oil, and as a treatment liquid for acidic waste liquid discharged from paper mills, etc.
更に、従来トルエン、ラッカー・シンナー等を溶剤とし
て用いざるを得なかったエポキシ系塗料、アクリル系塗
料の溶剤としても適用することができる。これらの塗料
は水酸化すトリウl\水溶液にも溶かすことができるが
、水酸化すI−リウl、水溶液の場合、塗料の粘性が増
し、溶剤として不適当であった。しかし、本発明の強塩
基性溶液の場合、粘性の上昇はなく、混合状態、塗布性
共に良好である。Furthermore, it can also be applied as a solvent for epoxy paints and acrylic paints, which conventionally had to use toluene, lacquer thinner, etc. as solvents. These paints can also be dissolved in an aqueous solution of sodium trihydroxide, but in the case of an aqueous solution of sodium trihydroxide, the viscosity of the paint increases, making it unsuitable as a solvent. However, in the case of the strongly basic solution of the present invention, there is no increase in viscosity, and both the mixing state and the coating properties are good.
以下余白
表1
本願の第二の発明である固体強塩基は、この強塩基性溶
液(b)を加熱して水分を蒸発させることにより得られ
る。強塩基性溶液(b)は極めて強い塩基性を有するの
で、これを加熱下で水分を除去する場合、耐腐性のある
容器が必要となる。Margin Table 1 Below: The solid strong base, which is the second invention of the present application, can be obtained by heating this strong basic solution (b) to evaporate water. Since the strongly basic solution (b) has extremely strong basicity, when removing moisture from it under heating, a container with corrosion resistance is required.
水分の除去は減圧で比較的低温で行うことも可能である
。Moisture removal can also be carried out under reduced pressure and at relatively low temperatures.
このようにして得られた固体強塩基は潮解性を有するこ
となく砂状の白い固体であった。主としてに、Na、C
aの塩、酸化物及び水酸化物であリ、水に溶かした際、
極めて強い塩基性を示すことからN a−Ca○等超強
塩基といわれる化合物をも含有すると推定される。The solid strong base thus obtained was a sandy white solid without deliquescent properties. Mainly Na, C
Salts, oxides and hydroxides of a, when dissolved in water,
Since it exhibits extremely strong basicity, it is estimated that it also contains compounds called super strong bases such as Na-Ca○.
この固体強塩基は水に溶解することによって第一の発明
である強塩基性溶液として用いることができ、特に液体
と違って運搬が容易であり、使用する場所で適宜調整で
きるという利点がある。By dissolving this solid strong base in water, it can be used as a strong basic solution according to the first invention, and has the advantage that unlike a liquid, it is easy to transport and can be adjusted appropriately at the site of use.
更に本発明の固体強塩基はその触媒作用を利用すること
ができ、燃焼反応の触媒として例えばアルコールと混練
することによりガソリン等の改質剤として適用すること
ができる。Further, the solid strong base of the present invention can utilize its catalytic action, and can be used as a combustion reaction catalyst, for example, as a reforming agent for gasoline etc. by kneading it with alcohol.
[実施例]
本発明の強塩基性溶液及び固体強塩基の製造方法の一実
施例を説明する。[Example] An example of the method for producing a strong basic solution and solid strong base of the present invention will be described.
1、P−8酸の調製
真水IQに動物骨の焼成物からなるリン酸カルシウムを
主成分とする粉末50gを溶解し、p I(13以上の
水溶液を得た。水溶液に対し5%の濃硫酸を加え、pH
0,2のP−8酸を製造した。1. Preparation of P-8 acid Dissolve 50 g of powder mainly composed of calcium phosphate made from calcined animal bones in fresh water IQ to obtain an aqueous solution with p I (13 or more). Add 5% concentrated sulfuric acid to the aqueous solution. addition, pH
0.2 P-8 acid was prepared.
2゜海水分離
海水500 Qに対し、上記のp−s酸10Qを加え、
3時間放置した後、不純物を濾過により除去した。これ
により海水はpH1,,6となった。次いで、低p、
H化した海水500Qに3%Na−〇■1水溶液を25
11を加え10時間放置した。この時、生成した沈澱物
を濾別後の溶液(a)のp、 Hは13.5であった。2゜Separated seawater Add 10Q of the above p-s acid to 500Q of seawater,
After standing for 3 hours, impurities were removed by filtration. As a result, the pH of the seawater became 1.6. Then low p,
Add 25% 3% Na-〇■1 aqueous solution to 500Q of hydrogenated seawater.
11 was added and left to stand for 10 hours. At this time, the p and H values of solution (a) after filtering off the generated precipitate were 13.5.
3、強塩基性溶液の製造
海水を分離した後の溶液(a)10Qを加熱して水分を
除去し、1.5Q、の濃縮溶液とした。この濃縮溶液を
急冷させることによって析出した沈澱物を除去し、目的
の強塩基性溶液を得た。除去した沈澱物は200gであ
った。3. Preparation of strongly basic solution Solution (a) 10Q after separating the seawater was heated to remove water to obtain a concentrated solution of 1.5Q. By rapidly cooling this concentrated solution, the precipitate deposited was removed to obtain the desired strong basic solution. The amount of precipitate removed was 200 g.
4、固体強塩基の製造
3で製造した強塩基性溶液(30kg)を石英性るつぼ
で加熱し、水分を蒸発させることにより目的の固体強塩
基(約5kg)を得た。4. Production of solid strong base The strong basic solution (30 kg) produced in step 3 was heated in a quartz crucible to evaporate water to obtain the target solid strong base (approximately 5 kg).
[発明の効果]
以上の説明からも明らかなように本発明の強塩基は、水
酸化ナトリウムに代わる、水酸化すトすラムより優れた
性質を有するものであり、工業」二幅広く利用すること
が可能である。[Effects of the Invention] As is clear from the above explanation, the strong base of the present invention has superior properties to sodium hydroxide, which can replace sodium hydroxide, and can be widely used in industry. is possible.
更に、本発明の強塩基は海水を用いて製造されるもので
あるから安価かつ大量に製造することができ、その製造
方法も容易である。Furthermore, since the strong base of the present invention is produced using seawater, it can be produced at low cost and in large quantities, and the method for producing it is also easy.
代理人 弁理士 守 谷 −雄Agent Patent Attorney Moriya - Yu
Claims (1)
しその際生成する沈澱物を除去して得られた溶液(a)
を濃縮後、冷却し、冷却の際生成する沈澱物を除去する
ことによって得られる溶液(b)から成る強塩基性溶液
。 2、第1項記載の超強塩基である溶液(b)から水分を
除去することによって得られる固体強塩基。[Claims] 1. Solution (a) obtained by making seawater acidic and then adding a strong alkaline agent to increase the pH and removing the precipitate generated at that time.
A strongly basic solution consisting of solution (b) obtained by concentrating, cooling, and removing the precipitate formed during cooling. 2. A solid strong base obtained by removing water from the solution (b) which is the super strong base described in item 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10680188A JPH01278593A (en) | 1988-04-28 | 1988-04-28 | Strongly basic solution and solid strong base |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10680188A JPH01278593A (en) | 1988-04-28 | 1988-04-28 | Strongly basic solution and solid strong base |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01278593A true JPH01278593A (en) | 1989-11-08 |
| JPH0583111B2 JPH0583111B2 (en) | 1993-11-24 |
Family
ID=14442976
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10680188A Granted JPH01278593A (en) | 1988-04-28 | 1988-04-28 | Strongly basic solution and solid strong base |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01278593A (en) |
-
1988
- 1988-04-28 JP JP10680188A patent/JPH01278593A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0583111B2 (en) | 1993-11-24 |
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