JPS6057918B2 - Seawater desalination method - Google Patents
Seawater desalination methodInfo
- Publication number
- JPS6057918B2 JPS6057918B2 JP52010133A JP1013377A JPS6057918B2 JP S6057918 B2 JPS6057918 B2 JP S6057918B2 JP 52010133 A JP52010133 A JP 52010133A JP 1013377 A JP1013377 A JP 1013377A JP S6057918 B2 JPS6057918 B2 JP S6057918B2
- Authority
- JP
- Japan
- Prior art keywords
- seawater
- scale
- acid
- salt
- seawater desalination
- 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
Links
Description
【発明の詳細な説明】
本発明は海水の淡水化方法、更に詳しくは海水を加熱蒸
発させて淡水を得るに当り、加熱蒸発装置へのスケール
の付着を防止し、効率良く淡水化を行なう方法に関する
。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a method for desalinating seawater, more specifically, a method for efficiently desalinating seawater by preventing scale from adhering to a heating evaporation device when heating and evaporating seawater to obtain fresh water. Regarding.
従来より海水を加熱蒸発後凝縮させ淡水を得る方法は、
例えば多段フラッシュ方式、管式多重効用方式又は浸管
方式等の各種加熱蒸発装置により実施されている。The conventional method of obtaining fresh water is to heat and evaporate seawater and then condense it.
For example, this is carried out using various heating evaporation devices such as a multi-stage flash method, a tube-type multiple effect method, or an immersion tube method.
しかるに上記各種装置による海水の淡水化において、海
水は加熱蒸発に伴い高濃度に濃縮される結果、その含有
するMgイオン、Caイオン等を炭酸塩、硫酸塩又は水
酸化物等の形態で析出し、之等が上記装置内特に伝熱面
にスケールとして付着する。このスケールの付着によれ
ば、伝熱面の伝熱係数は著しく低下し、淡水化の効率が
極端に低下し、ひいては運転が不可能となるという重大
な弊害が生じる。殊に海水は一般淡水と比較して通常約
100倍のオーダーの塩類を含有しており、Mgイオン
、Caイオン等の含有量も多く、上記スケーール付着の
傾向は特に著しい。従つて従来よりこの種海水の淡水化
方法においては、被処理海水に硫酸等の酸を加えPHを
調節して装置内でのスケール発生及び析出付着を防止す
る方法等が開発されている。しかるに酸を添加してpH
の調節によりスケールの発生を防止する方法では、装置
材料等の酸による腐食が新たな問題となり、しかもスケ
ール成分の分解に要する酸添加量は非常に多く更に通常
硫酸等の強酸を用いるためその取扱いにも危険を伴い実
用上満足な方法とはいえない。また重合リン酸を始めと
して、工業用水(硬水)のスケール防止に利用されてい
る各種スケール防止剤を添加する方法も種々提案されて
いる。しカルながら海水は一般工業用水とは異なりスケ
ール付着が著しく、通常のスケール防止剤は、その汎用
される濃度での使用によつては到底充分なスケール防止
効果を奏し得ないばかりか、比較的多量の使用によつて
も尚実用できるスケール抑制作用を奏し得ない。しかも
上記海水の淡水化においては被処理水は高温下に高濃縮
されるため、高温で容易に加水分解してそのスケール防
止能を消失する重合リン酸塩等は実際上使用に耐えずむ
しろその使用によれば加水分解により生成するオルトリ
ン酸がCaイオン、Mgイオンと不溶性塩を形成し逆に
スケールの因子となる。この様に従来海水の淡水化にお
いては満足なスケール防止法が未だ開発されておらず、
淡水化の効率を向上し得ない現状にある。本発明は上記
現状に鑑み海水の淡水化において重大な問題となつてい
るスケール付着を抑制し、安全で且つ効率よくしかも低
ランニングコストで運転可能な新しい海水の淡水化法を
提供することを目的とするものてある。However, when seawater is desalinated using the various devices mentioned above, the seawater is heated and evaporated to a high concentration, resulting in the Mg ions, Ca ions, etc. contained therein being precipitated in the form of carbonates, sulfates, hydroxides, etc. , etc. adhere as scale inside the above-mentioned apparatus, especially on the heat transfer surface. The adhesion of this scale significantly reduces the heat transfer coefficient of the heat transfer surface, extremely reducing the desalination efficiency, and eventually making operation impossible, which is a serious problem. In particular, seawater usually contains about 100 times as much salt as ordinary fresh water, and also has a large content of Mg ions, Ca ions, etc., so the tendency of scale adhesion is particularly remarkable. Therefore, in this type of seawater desalination method, a method has been developed in which an acid such as sulfuric acid is added to the seawater to be treated to adjust the pH to prevent scale formation and precipitation in the equipment. However, by adding acid, the pH
In the method of preventing scale formation by controlling the amount of water, a new problem arises: acid corrosion of equipment materials, etc. Moreover, the amount of acid required to decompose the scale components is extremely large, and since strong acids such as sulfuric acid are usually used, handling is difficult. However, it is not a practically satisfactory method as it is also dangerous. Various methods have also been proposed for adding various scale inhibitors, including polymerized phosphoric acid, which are used to prevent scale in industrial water (hard water). However, unlike general industrial water, seawater has significant scale adhesion, and ordinary scale inhibitors, when used at commonly used concentrations, are not only unable to produce sufficient scale prevention effects, but also have relatively low scale adhesion. Even when used in large quantities, it still cannot produce a practical scale-inhibiting effect. Moreover, in the desalination of seawater mentioned above, the water to be treated is highly concentrated at high temperatures, so polymerized phosphates, etc., which easily hydrolyze at high temperatures and lose their scale prevention ability, cannot withstand practical use, rather they are When used, orthophosphoric acid produced by hydrolysis forms insoluble salts with Ca ions and Mg ions, and conversely becomes a factor of scale. As described above, a satisfactory scale prevention method has not yet been developed for seawater desalination.
The current situation is that it is impossible to improve the efficiency of desalination. In view of the above-mentioned current situation, it is an object of the present invention to provide a new seawater desalination method that suppresses scale adhesion, which is a serious problem in seawater desalination, and that can be operated safely, efficiently, and at low running costs. There is something to do.
この目的は被処理海水にイソブテンー無水マレイン酸共
重合体またはその塩と、これに対し213乃至312倍
重量のホスホン酸またはその塩とを添加共存させること
により達成される。即ち本発明は上記イソブテンー無水
マレイン酸共重合体が優れたスケール防止能を有し、之
を上記所定量のホスホン酸と併用する時には、之等が相
乗的に作用し合つて少量の添加で卓越したスケール防止
効果を発揮ししかもその効果は高温条件下でも全く低下
せず従つて海水の淡水化におけるスケール付着の弊害を
一挙に解消できることを見い出し完成されたものである
。本発明において上記イソブテンー無水マレイン酸共重
合体としては好ましくは分子量1000〜150凹程度
のものを使用する。該共重合体のイソブテンと無水マレ
イン酸との共重合割合は特に制限されないが通常イソブ
テン含量が20〜70%程度好ましくは50%前後とす
るのがよい。また上記共重合体はその水に対する溶解性
を更に向上させるために例えばナトリウム、カリウム等
のアルカリ金属塩やアンモニウム塩の形態で用いること
ができる。また上記イソブテンー無水マレイン酸共重合
体またはその塩と併用されるホスホン酸及びその塩とし
ては、各種のホスホン酸、ホスホノカルボン酸及びそれ
らの水溶性塩類が使用できる。具体的には、ヒドロキシ
エタンー1,1ージホスホン酸、アミノエタンー1,1
ージホスホン酸、ヒドロキシプロパンー1,1ージホス
ホン酸、アミノトリメチルホスホン酸、エチレンジアミ
ンテトラメチルホスホン酸、ヘキサメチレンジアミンテ
トラメチルホスホン酸等のホスホン酸、1−ホスホノプ
ロパンー2,3−ジカルボン酸、1,1−ジホスホノプ
ロパンー2,3−ジカルボン酸、2ーホスホノブタンー
1,2−ジカルボン酸、2,2−ジホスホノプロパンー
3,4−ジカルボン酸等のホスホノアルカンジカルボン
酸;1−ホスホノプロパンー1,2,3−トリカルボン
酸、2−ホスホノブタンー1,2,4−トリカルボン酸
、2−ホスホノー3−(2−メチルカルボキシメチル)
−ヘキサンー1J2,4−トリカルボン酸等のホスホノ
アルカントリカルボン酸;及び乃等各化合物のアルカリ
金属塩、アンモニウム塩等を例示できる。上記共重合体
又はその塩とホスホン酸又はその塩との併用割合は、前
者10〜9哩量%及び後者10〜9呼量%の範囲で略々
併用効果を奏し得るが、少量の添加で常に安定して充分
なスケール防止効果を奏するためには前者40〜(1)
重量%及び後者40〜6踵量%とするのがよい。This object is achieved by adding and coexisting an isobutene-maleic anhydride copolymer or a salt thereof and a phosphonic acid or a salt thereof in an amount of 213 to 312 times the weight of the copolymer to the seawater to be treated. That is, the present invention provides that the above-mentioned isobutene-maleic anhydride copolymer has excellent scale prevention ability, and when it is used in combination with the above-mentioned predetermined amount of phosphonic acid, they act synergistically and achieve excellent scale prevention even with a small amount of addition. This product was developed based on the discovery that it exhibits a scale-preventing effect that does not deteriorate at all even under high-temperature conditions, and that it can eliminate the negative effects of scale adhesion in seawater desalination at once. In the present invention, the isobutene-maleic anhydride copolymer preferably has a molecular weight of about 1,000 to 150. The copolymerization ratio of isobutene and maleic anhydride in the copolymer is not particularly limited, but the isobutene content is usually about 20 to 70%, preferably about 50%. Further, the above copolymer can be used in the form of an alkali metal salt such as sodium or potassium, or an ammonium salt in order to further improve its solubility in water. Further, as the phosphonic acid and its salt used together with the isobutene-maleic anhydride copolymer or its salt, various phosphonic acids, phosphonocarboxylic acids, and water-soluble salts thereof can be used. Specifically, hydroxyethane-1,1-diphosphonic acid, aminoethane-1,1
Phosphonic acids such as -diphosphonic acid, hydroxypropane-1,1-diphosphonic acid, aminotrimethylphosphonic acid, ethylenediaminetetramethylphosphonic acid, hexamethylenediaminetetramethylphosphonic acid, 1-phosphonopropane-2,3-dicarboxylic acid, 1,1- Phosphonoalkanedicarboxylic acids such as diphosphonopropane-2,3-dicarboxylic acid, 2-phosphonobutane-1,2-dicarboxylic acid, 2,2-diphosphonopropane-3,4-dicarboxylic acid; 1-phosphonopropane-3,4-dicarboxylic acid; Nopropane-1,2,3-tricarboxylic acid, 2-phosphonobutane-1,2,4-tricarboxylic acid, 2-phosphono-3-(2-methylcarboxymethyl)
Examples include phosphonoalkanetricarboxylic acids such as -hexane-1J2,4-tricarboxylic acid; and alkali metal salts and ammonium salts of each compound. The combination ratio of the above copolymer or its salt and phosphonic acid or its salt is approximately 10 to 9% by weight for the former and 10 to 9% by volume for the latter, but a small amount of addition can produce a combined effect. In order to always have a stable and sufficient scale prevention effect, the former 40~(1)
The latter is preferably 40 to 6% by weight.
その海水への添加量は海水中に0.5ppm程度以上好
ましくは0.5〜200ppmより好ましくは2〜20
ppmの濃度で存在する量とすればよく、従つて上記濃
度となる量を連続的又は間歇的に被処理海水に添加注入
すればよい。かくして本発明によれば海水中に上記イソ
ブテンー無水マレイン酸共重合体又はその塩とホスホン
酸又はその塩とを所定割合で添加共存させるのみで、之
等が従来例のないスケール防止剤として作用し、海水の
高温条件下での加熱蒸発及び海水の高濃縮化に実質的に
何ら影響されることなく優れたスケール防止能を発揮し
、その淡水化を極めて効率よく実施可能とするのである
。The amount added to seawater is about 0.5 ppm or more, preferably 0.5 to 200 ppm, more preferably 2 to 20 ppm.
It is sufficient that the amount is present at a concentration of ppm, and therefore, the amount that has the above concentration may be continuously or intermittently added to the seawater to be treated. Thus, according to the present invention, by simply adding and coexisting the above-mentioned isobutene-maleic anhydride copolymer or its salt and phosphonic acid or its salt in seawater at a predetermined ratio, they act as an unprecedented scale inhibitor. It exhibits excellent scale prevention ability without being substantially affected by thermal evaporation of seawater under high-temperature conditions and high concentration of seawater, making desalination of seawater extremely efficient.
本発明における上記海水の淡水化装置、操作、運転条件
等は常法に従えばよい。又本発明方法においては更に必
要に応じてシリコンオイルや非イオン活性剤等の公知の
消泡剤を添加併用することも可能である。以下本発明を
更に詳しく説明するために実施例を挙げる。The seawater desalination apparatus, operation, operating conditions, etc. in the present invention may be carried out in accordance with conventional methods. In addition, in the method of the present invention, it is also possible to add and use known antifoaming agents such as silicone oil and nonionic activators, if necessary. Examples will be given below to explain the present invention in more detail.
実施例
1fビーカーに海水11を入れ、、これに各スケール防
止剤の夫々所定量を添加し、この海水中に熱源としてバ
イブヒーター(100■、500W)を浸漬し、これを
通電加温して、攪拌しながら蒸発濃縮を行う。Example 1f Seawater 11 was placed in a beaker, a predetermined amount of each scale inhibitor was added thereto, a vibrator heater (100cm, 500W) was immersed as a heat source in this seawater, and heated by electricity. , Evaporate and concentrate while stirring.
Claims (1)
イソブテン−無水マレイン酸共重合体またはその塩と、
これに対し2/3乃至3/2倍重量のホスホン酸または
その塩とを添加共存させて加熱蒸発装置へのスケールの
付着を防止することを特徴とする海水の淡水化方法。1. When heating and evaporating seawater to obtain fresh water, isobutene-maleic anhydride copolymer or its salt is added to the seawater,
A seawater desalination method characterized in that 2/3 to 3/2 times the weight of phosphonic acid or a salt thereof is added to coexist with the seawater to prevent scale from adhering to the heating evaporator.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52010133A JPS6057918B2 (en) | 1977-01-31 | 1977-01-31 | Seawater desalination method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52010133A JPS6057918B2 (en) | 1977-01-31 | 1977-01-31 | Seawater desalination method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5395185A JPS5395185A (en) | 1978-08-19 |
| JPS6057918B2 true JPS6057918B2 (en) | 1985-12-17 |
Family
ID=11741781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52010133A Expired JPS6057918B2 (en) | 1977-01-31 | 1977-01-31 | Seawater desalination method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6057918B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6071093A (en) * | 1983-09-27 | 1985-04-22 | Nippon Zeon Co Ltd | Water treating method |
| JPS61153198A (en) * | 1984-12-26 | 1986-07-11 | Nippon Zeon Co Ltd | Anti-scaling agent |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1414918A (en) * | 1973-02-14 | 1975-11-19 | Ciba Geigy Uk Ltd | Treatment of water to prevent the deposition of scale |
-
1977
- 1977-01-31 JP JP52010133A patent/JPS6057918B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5395185A (en) | 1978-08-19 |
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