JPS60114391A - Removing method of silica in water - Google Patents

Removing method of silica in water

Info

Publication number
JPS60114391A
JPS60114391A JP21867083A JP21867083A JPS60114391A JP S60114391 A JPS60114391 A JP S60114391A JP 21867083 A JP21867083 A JP 21867083A JP 21867083 A JP21867083 A JP 21867083A JP S60114391 A JPS60114391 A JP S60114391A
Authority
JP
Japan
Prior art keywords
silica
water
polymer
contg
thioether
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
JP21867083A
Other languages
Japanese (ja)
Other versions
JPS6339303B2 (en
Inventor
Yasuo Namita
靖夫 波田
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.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan 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 Idemitsu Kosan Co Ltd filed Critical Idemitsu Kosan Co Ltd
Priority to JP21867083A priority Critical patent/JPS60114391A/en
Publication of JPS60114391A publication Critical patent/JPS60114391A/en
Publication of JPS6339303B2 publication Critical patent/JPS6339303B2/ja
Granted legal-status Critical Current

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  • Physical Water Treatments (AREA)
  • Removal Of Specific Substances (AREA)
  • Water Treatment By Sorption (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

PURPOSE:To remove effectively silica contained in water with a simple installation and operation by bringing the thioether polymer expressed by the specified general formula into contact with water contg. silica and separating the polymer phase and the water phase. CONSTITUTION:The thioether polymer expressed by the formula [in which, A, B may be the same or different and denote respectively -H, -SH, -X (X denotes halogen atom), n, m denote respectively the numbers satisfying 4<=m<=2, 5<=n<= 200] is charged into the silica-contg. water stored in a tank or the silica-contg. water flowing in a pipe and the water is stirred and mixed. The amt. of the thioether polymer may be increased or decreased according to the concn. of silica. The contact time between said polymer and the silica-contg. water is such time when the concn. of the silica in the water after the treatment is <=200ppm.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は水中に存在するシリカ成分を除失する方法に関
し、更に詳しくは、チオエーテル重合体を用いた水中シ
リカの除去方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a method for removing silica components present in water, and more particularly to a method for removing silica in water using a thioether polymer.

〔発明の技術的背景とその問題点〕[Technical background of the invention and its problems]

天然水、とくに地熱利用の際に地下から汲みあげられる
熱水中には、溶解性シリカやコロイダルシリカが多量に
含有されている。
Natural water, especially hot water pumped up from underground during geothermal utilization, contains large amounts of soluble silica and colloidal silica.

そのため、配管系統や熱水利用の機器類にはシリカがス
ケールとして析出し、配管や機器類の閉塞事故がしばし
ば起る。
As a result, silica precipitates as scale in piping systems and equipment that utilizes hot water, often causing blockage accidents in piping and equipment.

このような事故への対策としては、通常、汲み上げる天
然水に各種の陽イオン成分を添加したり、コロイダルシ
リカを帯電させて析出を抑制したり、各種の凝集剤、シ
リカ捕集剤を添加したのち沈澱分離、遠心分離処理を施
すという方法が講じられている。
Measures to prevent such accidents include adding various cationic components to the natural water being pumped, charging colloidal silica to suppress precipitation, and adding various flocculants and silica scavengers. A method has been adopted in which the material is then subjected to precipitation separation and centrifugation treatment.

しかしながら、上記した方法はいずれもその操作が煩雑
でしかも処理に長時間を要するという問題がある。
However, all of the above methods have problems in that the operations are complicated and the processing takes a long time.

〔発明の目的〕[Purpose of the invention]

本発明は上記した問題を解決し、簡単な設備・操作で水
中に含有されるシリカを効果的に除去する方法の提供を
目的とする。
The present invention aims to solve the above problems and provide a method for effectively removing silica contained in water using simple equipment and operations.

〔発明の概要〕[Summary of the invention]

本発明方法は、 次式:A÷(CH2) m S垢B (式中、A、Bは同じであっても異なっていてもよく、
それぞれ−H,−8H,−X (ただし、Xはハロゲン
原子を表わす)を表わし;m、nはそれぞれ4≦m≦2
0,5≦n≦200の関係を満足する数を表わす) で示されるチオエーテル重合体をシリカ含有水に接触さ
せたのち、該重合体と水を分離することを特徴とする。
The method of the present invention is based on the following formula: A÷(CH2) mS sludge B (wherein A and B may be the same or different,
Each represents -H, -8H, -X (where X represents a halogen atom); m and n each represent 4≦m≦2
The method is characterized in that after a thioether polymer represented by the formula (representing a number satisfying the relationship of 0,5≦n≦200) is brought into contact with silica-containing water, the polymer and water are separated.

本発明方法は、上記したチオエーテル重合体を用いるこ
とに最大の特徴がある。
The method of the present invention has the greatest feature in using the above-mentioned thioether polymer.

このチオエーテル重合体は、+(CH2)m−8+を繰
返し単位とするもので、その末端は−H,−8H。
This thioether polymer has +(CH2)m-8+ as a repeating unit, and its terminal ends are -H and -8H.

−X(ただし、Xはハロゲン原子を表わす)のいずれか
でブロックされている。すなわち、前記の式%式% ある。また、A、Bは同じであっても、異なっていても
よい。Xとしては、ハロゲン原子であれば何であっても
よいが、チオエーテル重合体の製造のし易さからすると
XはBr又はClであることが好ましい。
-X (where X represents a halogen atom). That is, the above formula % formula % exists. Further, A and B may be the same or different. X may be any halogen atom, but from the viewpoint of ease of manufacturing the thioether polymer, X is preferably Br or Cl.

繰返し単位におけるメチレン基の数mは4以上20以下
である。mが4未満の場合には重合体は液状となって扱
いに〈〈なり、また20を超える場合には該重合体の、
融点が高くなりまた硫黄原子の含有量が減じその結果、
効果が小さくなる。
The number m of methylene groups in the repeating unit is 4 or more and 20 or less. When m is less than 4, the polymer becomes liquid and becomes difficult to handle, and when m exceeds 20, the polymer becomes
The melting point increases and the content of sulfur atoms decreases, resulting in
The effect becomes smaller.

好ましくは5〜12である。Preferably it is 5-12.

更に上記した繰返し単位の数nは5以上200以下であ
る。nが5より小さい場合には、水に対し混和し易くな
り水との分離が困難となって不都合であり、また200
を超える場合には、充分なシリカ捕集効果が発揮されな
い。好ましくは7〜100である。
Furthermore, the number n of repeating units described above is 5 or more and 200 or less. When n is less than 5, it is disadvantageous because it is easily miscible with water and difficult to separate from water.
If it exceeds 100%, sufficient silica trapping effect will not be exhibited. Preferably it is 7-100.

このようなチオエーテル重合体はX (CH2) m−
X (ただし、XはハClグン)、Na、S、水を出発
原料とし、触媒を用いて重合させるというような方法で
容易に製造することができる。
Such thioether polymers are X (CH2) m-
It can be easily produced by using as starting materials X (where X is Cl), Na, S, and water and polymerizing them using a catalyst.

本発明方法は次のようにして行なわれる。The method of the present invention is carried out as follows.

すなわち、まず、上記したチオエーテル重合体をシリカ
含有水に接触させる。接触の態様はいかなる方法でもよ
い。例えば、槽内に貯留したシリカ含有水又は管内を通
流するシリカ含有水に上記重合体を投入して撹拌・混合
する。
That is, first, the above-described thioether polymer is brought into contact with silica-containing water. The contact may be made in any manner. For example, the polymer is added to silica-containing water stored in a tank or flowing through a pipe, and stirred and mixed.

チオエーテル重合体の使用量は、シリカ濃度に応じて増
減させればよいので一義的には決められない。また、こ
の重合体とシリカ含有水との接触時間は、重合体の使用
量、原水のシリカ濃度及び処理後の水のシリカ濃度をど
の程度にまでするかという目的との関係で決められる。
The amount of the thioether polymer to be used cannot be determined uniquely because it can be increased or decreased depending on the silica concentration. Further, the contact time between the polymer and the silica-containing water is determined depending on the amount of the polymer used, the silica concentration of the raw water, and the silica concentration of the water after treatment.

通常は、処理後の水のシリカ濃度が200 ppm以下
になるような時間である。
Usually, the time is such that the silica concentration in the water after treatment becomes 200 ppm or less.

この接触時の温度は格別限宇されないが、チオエーテル
重合体の融点以上の温度下で接触させると、すなわち、
チオエーテル重合体を溶融状態で用いると、シリカ除去
効果が顕著に向上して有効である。
The temperature during this contact is not particularly limited, but if the contact is made at a temperature higher than the melting point of the thioether polymer, that is,
When the thioether polymer is used in a molten state, the silica removal effect is significantly improved and effective.

このようにして、シリカ含有水中のシリカはチオエーテ
ル重合体によって捕促される。シリカを捕促したチオエ
ーテル重合体は、沈澱として、又は処理後の水の中に分
散して存在する。
In this way, the silica in the silica-containing water is trapped by the thioether polymer. The thioether polymer entrapping the silica is present as a precipitate or dispersed in the water after treatment.

したがって、本発明にあっては次に、シリカを捕促した
チオエーテル重合体の相と水の相を分離する。
Therefore, in the present invention, next, the thioether polymer phase in which silica has been trapped and the water phase are separated.

両相の分離に際しては、常用の固液分離(沈澱のP別)
、液液分離(重合体が溶融している場合)処理などを適
宜に施せばよい。
When separating both phases, use conventional solid-liquid separation (separate P in precipitate).
, liquid-liquid separation (when the polymer is molten) treatment, etc. may be performed as appropriate.

〔発明の実施例〕[Embodiments of the invention]

実施例1 分子量約1000の式: H8−E−(CHI )6−
 S +Fr1Hで示されるチオエーテル重合体(融点
76℃)の粉20gを、コロイダルシリカ含量792 
ppmで全シリカ含量940 ppmの原水100dの
中に投入した。25℃の温度で重合体の粉と原水の系を
振とうしたのち、粉をP別して処理水中のコロイダルシ
リカ含量、全シリカ含量を測定した。
Example 1 Formula: H8-E-(CHI)6- with a molecular weight of about 1000
20 g of powder of a thioether polymer (melting point 76°C) represented by S + Fr1H was mixed with colloidal silica content of 792
It was poured into 100 d of raw water with a total silica content of 940 ppm. After shaking the polymer powder and raw water system at a temperature of 25° C., the powder was separated from P and the colloidal silica content and total silica content in the treated water were measured.

その結果を、振とう時間との関係として第1表に括して
示した。
The results are summarized in Table 1 as a relationship with shaking time.

第 1 表 実施例2 +:1rx−fk重合体が、式:HSモ(Cut)to
 5thH(分子量約11000.融点96°C)であ
ったことを除いては、実施例1と同様にして原水中のシ
リカを除去した。その結果を第2表に示した。
Table 1 Example 2 +:1rx-fk polymer has formula: HSMo(Cut)to
Silica in the raw water was removed in the same manner as in Example 1, except that it was 5thH (molecular weight approximately 11,000, melting point 96°C). The results are shown in Table 2.

第 2 表 実施例3 原水との接触時の温度が100℃であった、分離方法は
、処理系全体を静置して有機相と水相とを分離するとい
う方法であったことを除いては、実施例1と同様にして
シリカを除去した。接触時間10分後におけるコロイダ
ルシリカ、全シリカの含量はそれぞれ14 ppm、2
73 ppmであった。
Table 2 Example 3 The temperature at the time of contact with the raw water was 100°C, except that the separation method was to leave the entire treatment system still and separate the organic phase and the aqueous phase. Silica was removed in the same manner as in Example 1. After 10 minutes of contact time, the contents of colloidal silica and total silica were 14 ppm and 2 ppm, respectively.
It was 73 ppm.

実施例4 原水との接触時の温度が100℃であったことを除いて
は、実施例2と同様にしてシリカを除去した。接触時間
10分後におけるコロイダルシリカ、全シリカの含量は
それぞれ21ppm、284ppmであった。
Example 4 Silica was removed in the same manner as in Example 2, except that the temperature during contact with raw water was 100°C. After a contact time of 10 minutes, the contents of colloidal silica and total silica were 21 ppm and 284 ppm, respectively.

実施例5 式’ H8+ (CHt )e S +f−H(分子量
約4200 。
Example 5 Formula 'H8+(CHt)eS+f-H (molecular weight approximately 4200.

融点42℃)で示されるチオエーテル重合体を用いたこ
と、接触時の温度が50℃であったことを除いては、実
施例1と同様にして原水中のシリカを除去した。接触時
間10分後のコロイダルシリカ、全シリカの含量はそれ
ぞれ15 ppm、301ppmであった。
Silica in the raw water was removed in the same manner as in Example 1, except that a thioether polymer having a melting point of 42°C was used and the temperature during contact was 50°C. After a contact time of 10 minutes, the contents of colloidal silica and total silica were 15 ppm and 301 ppm, respectively.

〔発明の効果〕〔Effect of the invention〕

以上の説明で明らかなように、本発明方法は、■極めて
簡単な操作、装置で水中のシリカを除去できる、■シリ
カ除去に必要な時間が比較的短い、などの効果を奏し、
天然水を直接使用する産業分野、地熱発電の分野、鉱業
関係の分野などに適用してその工業的価値は大である。
As is clear from the above explanation, the method of the present invention has the following effects: 1. Silica in water can be removed with extremely simple operation and equipment; 2. The time required for silica removal is relatively short.
It has great industrial value when applied to industries that directly use natural water, geothermal power generation, mining-related fields, etc.

Claims (1)

【特許請求の範囲】 1、次式:A千(CH2) m 5−)−B(式中、A
、Bは同じであっても異なっていてもよく、それぞれ−
H,−8H,−X (ただし、Xはハロゲン原子を表わ
す)を表わし;m、nはそれぞれ4≦m≦20,5≦n
≦200の関係を満足する数を表わす)で示されるチオ
エーテル重合体をシリカ含有水に接触させたのち、該重
合体の相と水の相を分離することを特徴とする水中シリ
カの除去方法。 2、該接触時の温度が、該チオエーテル重合体の融点以
上の温度である特許請求の範囲第1項記載の方法。
[Claims] 1. The following formula: A 1,000 (CH2) m 5-)-B (in the formula, A
, B may be the same or different, and each -
H, -8H, -X (where X represents a halogen atom); m and n are 4≦m≦20, 5≦n, respectively
A method for removing silica in water, the method comprising: contacting a thioether polymer (representing a number satisfying the relationship of ≦200) with silica-containing water, and then separating the polymer phase and the water phase. 2. The method according to claim 1, wherein the temperature during the contact is higher than the melting point of the thioether polymer.
JP21867083A 1983-11-22 1983-11-22 Removing method of silica in water Granted JPS60114391A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21867083A JPS60114391A (en) 1983-11-22 1983-11-22 Removing method of silica in water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21867083A JPS60114391A (en) 1983-11-22 1983-11-22 Removing method of silica in water

Publications (2)

Publication Number Publication Date
JPS60114391A true JPS60114391A (en) 1985-06-20
JPS6339303B2 JPS6339303B2 (en) 1988-08-04

Family

ID=16723579

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21867083A Granted JPS60114391A (en) 1983-11-22 1983-11-22 Removing method of silica in water

Country Status (1)

Country Link
JP (1) JPS60114391A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11244867A (en) * 1998-02-27 1999-09-14 Mitsubishi Materials Corp Treatment of silica-containing geothermal hot water
JP2007321885A (en) * 2006-06-01 2007-12-13 Mirai Ind Co Ltd Connection structure of double-walled pipe to coupling

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH058883Y2 (en) * 1986-12-17 1993-03-05

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11244867A (en) * 1998-02-27 1999-09-14 Mitsubishi Materials Corp Treatment of silica-containing geothermal hot water
JP2007321885A (en) * 2006-06-01 2007-12-13 Mirai Ind Co Ltd Connection structure of double-walled pipe to coupling

Also Published As

Publication number Publication date
JPS6339303B2 (en) 1988-08-04

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