JPH0259094A - Ph control method - Google Patents

Ph control method

Info

Publication number
JPH0259094A
JPH0259094A JP21005888A JP21005888A JPH0259094A JP H0259094 A JPH0259094 A JP H0259094A JP 21005888 A JP21005888 A JP 21005888A JP 21005888 A JP21005888 A JP 21005888A JP H0259094 A JPH0259094 A JP H0259094A
Authority
JP
Japan
Prior art keywords
solvent
honeycomb
powder
sheet
container
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.)
Pending
Application number
JP21005888A
Other languages
Japanese (ja)
Inventor
Takaharu Asano
浅野 敬治
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP21005888A priority Critical patent/JPH0259094A/en
Publication of JPH0259094A publication Critical patent/JPH0259094A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0086Processes carried out with a view to control or to change the pH-value; Applications of buffer salts; Neutralisation reactions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)

Abstract

PURPOSE:To remove impurities and to easily control pH by a method wherein a metal oxide component is mixed with amorphous carbon particles having a metal ion adsorbed thereby and the formed powder is brought into contact with water containing impurities to adjust said water to predetermined pH. CONSTITUTION:A powder obtained by mixing a metal oxide component with amorphous carbon particles having a metal ion adsorbed thereby is used as it is or subjected to secondary processing. Subsequently, said powder is brought into contact with water containing impurities or an org. solvent for a definite time not only to purity the solvent but also to neutralize the same or to restor the pH of the original solvent to control pH. As the concrete example of the aforementioned metal ion, there are Na, K, Mg, Ca, Cr, Ni, Mn or Zn and, as the concrete example of metal oxide, there are Al2O3, SiO2 or Fe2O3. By this method, simultaneously with the removal of impurities, pH can be controlled without charging chemicals.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は水及び有慎俗剤が不細物に汚染され、そのPH
が変化したとき、その不H′#Jk吸虜浄化すると共に
PHを中性に近い伏7に回復させる方法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention deals with water and unscrupulous agents that are contaminated with impurities and whose PH
This method relates to a method for purifying the PH when the pH changes, and for recovering the pH to 7, which is close to neutrality.

(従来の技術) 工業用水或はその他の目的で門己管金流通すろ水の管理
に於込て、PHの+ilf’J顛及び不細物の問題は水
質の評価、b己管の安全上亜要な課題である。多くの場
合、水のpHX、化は不純物の存在によって生じるが、
他面ば目的に変えることもあシ、そのための方法として
、は不細物を除去するか、薬品を投入してPHを調節す
るのである。
(Prior art) In the management of effluent flowing through pipes for industrial use or other purposes, the problems of PH, filtrate, and impurities are important for evaluating water quality and for the safety of pipes. This is an important issue. In many cases, the pH of water changes due to the presence of impurities.
On the other hand, it is also possible to change it for other purposes, and the methods for that purpose are to remove impurities or to adjust the pH by adding chemicals.

(究明が、91決しようとする課題〉 不−B物を除去する方法としては濾過模、又は活性法の
ような吸層剤全使用するのが最も一服的であるが、これ
らの使用目的はPHの調節を慧図するものではないので
、PHに影響を及ぼす不純物を除去するとPHが元の伏
惑にLSI狽するに過ぎない。
(Issues to be solved by investigation) The most effective method for removing non-B substances is to use all absorbing agents such as filtration or activation methods, but the purpose of these uses is Since it is not intended to control the pH, removing impurities that affect the pH will only make the LSI return to its original state.

これに対し、1図的にPHを調節する場合は酸又はアル
カリの薬品を投入する。例えば原子発電所の冷却水にL
i  (OH)を投入し、OHイオンの濃度ヲ営理する
とか、上水道の配fII5蝕を防止するためにカルシウ
ム化合物ニよるOHイオンの投入等がある。
On the other hand, when adjusting the pH in one diagram, acid or alkali chemicals are added. For example, L is used for cooling water in nuclear power plants.
i (OH) to control the concentration of OH ions, or to prevent water supply from corrosion by adding OH ions using calcium compounds.

このような薬品投入方式は化学的にPHr調如する目的
としては最も単tnHで効果的な手段であるが、しかし
薬品投入方法では必ず反対側のイオンが残留することと
なシ、殆んどの場合この残留物は望しくない物資である
This type of chemical injection method is the most effective means for chemically adjusting PHr with a single tnH, but in most chemical injection methods, ions on the opposite side always remain. In this case, this residue is an undesirable material.

また工業的に広く使われている・H機廖則の場合、使用
する間に不、−れ物が混入され鹸江又は7ルカリ姓に変
化する。このPHcl父1とと押えるために、また有(
張俗剤の使用ガ晴金長くするために有蝋溶剤中の不純物
を除去することが重要であシ、その方を人として炉暎或
ンよ活性法のような多孔体の物理的吸4’材が用いられ
るのであるが、不純物を除去した後も必要に応じ薬品を
投入してPHを調節する。
In addition, in the case of the ``H Machine Liao Rule'' which is widely used in industry, foreign substances are mixed in during use and the surname changes to Kenjiang or 7 Lucari. In order to suppress this PHcl father 1, there is also (
It is important to remove impurities in the waxy solvent in order to prolong the use of the waxing agent, and it is better to remove the impurities from the waxy solvent by physically absorbing the porous material, such as using a furnace or an active method. Even after removing impurities, chemicals are added as needed to adjust the pH.

このように従来のPH調iIa技術は専ら薬品を投入す
ることであシ、それには必ず反対側のイオンに対する管
理を行わなければならない。
As described above, the conventional PH adjustment IIa technique involves exclusively injecting chemicals, and in doing so, the ions on the opposite side must be managed.

(課題を解決するための手段) 本究明は上記問題点を解決せんとするものであって蛍、
萬イオンを扱盾した非゛晶質炭素粒子に金属酸1ヒ吻成
分を混合した粉末(以下、粉本と称す)を粉末のま\投
入、または2次加工(以下、加工品と称す)し、これを
不純物を含む水又は−Vflx l蓄剤(以下、水を含
め溶剤と称す)に一定時1lfJ接触させ、溶媒を浄化
すると共に、PHを中性化するか元のld謀のPHK回
硬させる(以下、浄化を含め調顛法と称す)ことを特徴
とする。
(Means for solving the problem) This research aims to solve the above problems.
Powder made by mixing amorphous carbon particles that handle 10,000 ions with one component of metal acid (hereinafter referred to as powder) is added to the powder or is subjected to secondary processing (hereinafter referred to as processed product). Then, this is brought into contact with impurity-containing water or -Vflx l storage agent (hereinafter referred to as the solvent including water) for 1lfJ for a certain period of time to purify the solvent and neutralize the PH, or to remove the original PHK from the LD scheme. It is characterized by hardening (hereinafter referred to as the preparation method including purification).

不発明で粉本の製造は金属イオンを非晶質仄素粒子に吸
着させ、その次素粒子に金属酸化物成分を混入して粉末
を:A整し、その粉末と固形粉末と固形粉末の非酸化物
又は酸化物戚は后注炭のような担体とを混合し、水又は
池のバインダーで固め、これを800℃以下でノ頂黙処
理して製造されるのであり、これに対し分散剤は非晶′
R次累を凡そ1戸以下の粉末となるように粉砕すると共
に、金属イオンの全て金含む有機分散剤と混合して金属
イオンを粉本の粒子表面に吸着させ、これを500℃以
下の乾燥工程中で凡そ1μm以下の金属酸化物粒子をl
尾大して製造するものである。
Inventive powder book manufacturing involves adsorbing metal ions onto amorphous particles, then mixing metal oxide components into the particles to prepare the powder, and then combining the powder with solid powder and solid powder. Non-oxides or oxides are produced by mixing with a carrier such as coal injection, solidifying with water or a binder, and then silently treating the mixture at a temperature below 800°C. The agent is amorphous
The R grade is crushed into a powder of approximately one size or less, mixed with an organic dispersant containing all metal ions to make the metal ions adsorb onto the surface of the powder particles, and dried at 500°C or less. Metal oxide particles of approximately 1 μm or less are removed during the process.
It is manufactured in large quantities.

(作用) 本発明では金ノ寓イオンを吸着した非晶質次素粒子に金
属酸化物成分を混合した粉末を利用するのであシ、これ
は非晶質汰素に吸)Hした金属イオンが触媒であってI
#、諷で物理的及び化学的吸清活性の高い物質である。
(Function) In the present invention, a powder is used in which a metal oxide component is mixed with amorphous elementary particles that have adsorbed metal ions. Catalyst I
#, literally, is a substance with high physical and chemical absorption activity.

金属イオンの鍍、アルカリ環境におけるCヒ学的挙動は
不明な点が多いが、水分子を分解しOHイオンを完生ず
ることがわかっている。
Although much is unknown about the chemical behavior of metal ions in an alkaline environment, it is known that they decompose water molecules and completely generate OH ions.

また含有物質であるA1903.5ICh、Flzoa
は持に層線のPH変化に灯影−を与えるものとなる。
In addition, the contained substances A1903.5ICh, Flzoa
It will give a light to the PH change of the layer line.

本発明は以下の火桶例及び夾験例によって具体的に説明
される。
The present invention is illustrated by the following fire barrel examples and experimental examples.

(実施例1) 第1図Aに於いてl?i扮末粉末分散剤の反入槽である
。該投入槽には攪拌方式が図示されていないが、自動又
は手動により槽内の攪拌が行わnる。攪拌が終9曾らく
放置すると粉本は投入槽の底辺に沈−するので浮液を流
出口2よシ流し、使用剤の粉末はドレン口3より除去す
る。但し、分散液を投入する場合id分散剤の比■が溶
媒と余シ差が認められないことが多く、この場合は攪拌
後放i%粱しても良い条件で行わなければならない。
(Example 1) In FIG. 1A, l? This is the anti-admission tank for powder dispersant. Although the stirring system for the charging tank is not shown in the drawings, the inside of the tank can be stirred automatically or manually. If the stirring is left for a long time, the powder will settle to the bottom of the input tank, so the floating liquid will flow through the outlet 2 and the powder of the agent used will be removed through the drain port 3. However, when adding a dispersion liquid, there is often no discernible difference in the ratio of id dispersant to that of the solvent, and in this case, it must be carried out under conditions that allow i% to be reduced after stirring.

使用する適量は不ボヒ物の一度によるが、粉本ly当り
溶解性物質を1009〜200岬吸肩1宗去する能力を
持っている。分散液体には1〜10%の粉本を分散する
ので粉本の含有量を考ノ、ばして最終結果を計算する。
The appropriate amount to use depends on the amount used, but it has the ability to remove 1,009 to 200 soluble substances per liter of powder. Since 1 to 10% of powder is dispersed in the dispersion liquid, the final result is calculated by taking into account the content of powder.

しかしてPHは不純物が除去されたあと弱アリカリ注の
M謀となる。
However, after the impurities are removed, the pH becomes weakly alkali.

本発明で固形体或はシート状の加工品は粉本のような直
接投入方式ではなく、m謀の流れを利用して接触させる
ようになされる。また、粉末の投入と異り、接m時間を
十分とってからrX、m分離するような工程は必要ない
ので長時間繰返して使用することができる。
In the present invention, the solid or sheet-like processed product is brought into contact with the product using a mechanical flow, rather than a direct feeding method such as a powder book. Furthermore, unlike the case of adding powder, there is no need for a step of allowing sufficient contact time before rX and m separation, so it can be used repeatedly for a long time.

ところで固形陣取はシート伏に加工する場合、その:汲
庸持注が粉末の場合と異るので当然PHの調節条件も異
るのであって、従って夫々れの吸渭特性を十分調べた上
で葉材及び装置の設計を行う。
By the way, when processing a solid sheet into a sheet, it is different from the powder, so naturally the pH adjustment conditions are also different, so the absorption characteristics of each should be thoroughly investigated. Design of leaf materials and equipment.

次に固形体の加工品によるPH調節法について説明する
。固形体の加工品はその形仄から多種のものが考えられ
、りlえば粒状、球状、ペレット伏、ハニカム伏などが
考えられる。
Next, a method of adjusting pH using a processed solid product will be explained. There are many types of solid processed products depending on their shape, including granular, spherical, pellet, and honeycomb shapes.

これらは常温でラングミアンの吸ja式でその吸>12
特性が説明されるが、吸漕速度は各形状によって多少の
相異があるもの″−概略M課ノ中テ0.4〜t # 7
g、灯程度である。これは通常の多孔体吸清剤、例えば
活性法と比較して若干遅い方である。そのために、突用
に於いては必要な層線を必要な時間内に処理するべく色
々な工夫が必要であるが、本発明では流入する層線に対
応する工Vメントを設計し、これを装置内へ適宜組込む
ようになすのである。
These have Langmian suction type at room temperature, and the suction is >12.
The characteristics will be explained, but the suction speed will differ slightly depending on the shape.
g, about the size of a light. This is a little slower than conventional porous absorbents, such as the activation method. For this reason, in emergency situations, it is necessary to take various measures to process the necessary layer wires within the required time, but in the present invention, we have designed a process that can handle the inflowing layer wires, and It is designed to be incorporated into the device as appropriate.

第11B?i該授14全ボアもので6って、1つのエレ
メントは溶媒の流れ・七−時的に貯留スるセクション5
と、固形体加工品を入れる容器6とからなシ、図示レリ
装置は上段に2圀、下段に21m1ld設されてなる。
11th B? 14 full-bore design, one element has a section 5 for solvent flow and temporary storage.
and a container 6 for holding the solid processed product, and the illustrated reli device is installed in the upper stage with 2 squares and the lower stage with 21 m1ld.

このさい7はセクション間を吐切る堰板、8は流入管、
9は流出管であって、流入管8から流入する俗峰?′i
堰板7を越えて順次67、幡ン5を矢印方向に流れ、且
つ上段からは下段に移行し同様谷1.2i4J25 k
流れて流出管9から排出される。本装置では液位が堰板
7の;離さに達するまでの時間層線と加工品が接i強す
るのであり、加工品入れ容器6は列えば金網のようなも
ので間に合うため、容品目体が接触に支障を与えること
はない。なお、1つのエレメントに於いて加工品入れ容
器6の取付は位置は三通りめる。即ち溶媒の比夏よりそ
こに含まれている不、4物の比重が大きい時には、不、
沌物の1n度は下方がj妬くなるので取付位置は中間よ
シ下に、比重が反対の場合は中間よシ上に取付け、何れ
の比重にも差が余シ側い1階は中間位置に取付けるよう
にする。
In this case, 7 is a weir plate for discharging between sections, 8 is an inflow pipe,
9 is the outflow pipe, and the common peak that flows in from the inflow pipe 8? 'i
It passes over the weir plate 7 and flows in the direction of the arrow in the direction of the arrow 67 and the gate 5, and from the upper stage to the lower stage, the same valley 1.2i4J25k
It flows and is discharged from the outflow pipe 9. In this device, the time layer line and the processed product are in close contact until the liquid level reaches the distance of the weir plate 7, and if the processed product container 6 is lined up, it can be made of something like a wire mesh, so the container does not interfere with contact. Note that the processed product container 6 can be attached to three positions in one element. In other words, when the specific gravity of the four substances contained in the solvent is greater than that of the solvent, the
Since the lower part of the 1n degree of the chaotic object is jealous, the installation position is below the middle.If the specific gravity is opposite, install it from the middle to the top.If there is no difference in any specific gravity, the first floor should be installed in the middle position. so that it is installed on the

ところで上述の如き加工品入れ容器6の取付は位置とか
、この#&g6を受答する各エレメントは溶媒中の不純
物の除去とPH調節に対して、加工品との接触時間を決
める亜要な要因となる。図示例で加工品入れ容器6はそ
の形状が同局形のものにしても艮く、またエレメントの
数を減す代わシに、エレメントの大きさを大きくするこ
ともできる。しかし、ニレメン)を大きくすることは使
用する現場条件とか、装置のコストを下げるr谷解注物
貿f:100sy〜200ダ県盾除去する能力金持って
いる0分散液体にはl −10%の粉末を分散するので
粉本の含有層を考L〆してkP−結果を計算する。しか
して、PHは不純物が除去されたあと剥アルカリ注の溶
媒どなる。
By the way, the mounting position of the processed product container 6 as mentioned above is a sub-important factor that determines the contact time with the processed product for the removal of impurities in the solvent and pH adjustment of each element that receives this #&g6. becomes. In the illustrated example, the processed product container 6 can have the same shape, and instead of reducing the number of elements, the size of the elements can be increased. However, increasing the size of the dispersion liquid depends on the field conditions used, lowering the cost of the equipment, and lowering the cost of the equipment. Since the powder is dispersed, the kP-result is calculated by considering the layer containing the powder. Therefore, the pH of the alkali stripping solvent increases after the impurities are removed.

本開明で固形体或はシート状の加工品は粉末のような直
接投入方式ではなく、溶媒の流れを利用して82触させ
るようになされる。また、粉本の投入と異シ、接触時間
を十分とって、からEm分離するような工程は必要ない
ので長時間繰返して使用することができる。
In the present invention, a solid or sheet-like processed product is not directly introduced like a powder, but is brought into contact using a flow of a solvent. In addition, since there is no need for steps such as loading the powder book, allowing sufficient contact time, and separating Em from it, it can be used repeatedly for a long time.

ところで固形体或はシート状に汀工する場合、その汲盾
特性が粉末O場合と異るので当然PHの調節条件も異る
のであって、従って大々れの1汲7M′4注全十分調べ
た上で素材及び賃1dの設計を行う。
By the way, when sanding in the form of a solid or sheet, the sanding characteristics are different from those of powder O, so naturally the pH adjustment conditions are also different. After researching, we will design the materials and rent 1d.

入に固形体の加工品によるPH調顛法について説明する
。固形体の加工品はその形状から多側のものが考えらn
、列えば粒状、球状、ベレット伏、ハニカム伏などが考
えられる。
First, we will explain the PH adjustment method using solid processed products. Solid processed products can be considered multi-sided due to their shape.
, granular, spherical, pellet shape, honeycomb shape, etc. can be considered.

これらは常温でラングミアンの・米層式でその吸肩特性
が説明されるが、咬着速度は谷形状によって多少の相異
があるもの一概略解謀の中で0.4〜lq/y、hr程
度である。これは通常の多孔体吸層剤、例えば活性法と
比較して肴干遅い方である。そのために、英用に於いて
は必要な溶媒を必要な時間内に処理するべく色々な工夫
が必要であるが、本発明では流入するtW Kに対応す
るニレメンt’−,&計し、これを装置内へ適宜組込む
ために艮くめることでbるが、この場合は溶μと加工品
との接触を悪くするのであって、極端な列としてはエレ
メントを11にして他の装置を省略することがある。
The shoulder suction characteristics of these are explained by the Langmian/Rice layer equation at room temperature, but the bite speed differs somewhat depending on the valley shape. It is about hr. This is slower drying than conventional porous absorbent agents, such as active methods. For this purpose, various measures are required in order to process the necessary solvent within the required time, but in the present invention, the nilemens t'-, & corresponding to the inflowing tWK are calculated, In order to properly incorporate it into the equipment, it is possible to make some adjustments, but in this case, the contact between the molten μ and the processed product will be poor, so in an extreme case, the number of elements can be set to 11 and other equipment can be omitted. Sometimes.

(夾施列2) 第2図は他の列のエレメントを示すもので、溶媒を受け
る谷姦は省略しである。このさい加工品10は円闇谷潴
11に詰められてめシ、溶媒の流入口12及び流出口1
3は流通に支障を与えない程度の隙間を有する蓋となっ
ている。本しリのエレメントは必要な量の俗縄を処理す
るために流圧が加えられる伏ルで使われることが多いの
で、強度のことを十分考りぼして作られる。
(Containment row 2) Figure 2 shows the elements of the other rows, and the valleys that receive the solvent are omitted. At this time, the processed product 10 is packed into the enyamidani tank 11, and the inlet 12 and outlet 1 for the solvent.
3 is a lid with a gap that does not impede circulation. Honshiri elements are often used in folding systems where fluid pressure is applied to process the necessary amount of rope, so they are made with sufficient strength in mind.

(夾苑列3) 本f/lはシート状加工品によるものであってシート状
加工品は削記粉末を更らに細く粉砕して作る。即ち、約
0.1〜0.01agK細分1ヒした粉末を水や熱を加
えて十分信託し乾糖したものを紙又はシート状物質とす
る。具体的には十分に分解されたパルプのスラリーへ池
の添)M剤と前記細分化粉末を除々に加えながら混合′
A侵し、調整したパルプスラリーを抄紙域へ送って紙状
に、製造するのである。
(Kyoen row 3) This f/l is a sheet-shaped processed product, and the sheet-shaped processed product is made by grinding the abrasive powder even finer. That is, the powder, which has been subdivided into about 0.1 to 0.01 agK, is sufficiently stirred with water and heat and dried to form a paper or sheet-like material. Specifically, the M agent and the finely divided powder are gradually added to a slurry of sufficiently decomposed pulp and mixed.
The pulp slurry that has been subjected to A-corrosion is sent to the papermaking area to be made into paper.

こ\にシート状加工品は粉末が更らに細分化されている
ために比表面積が大きく増加している。従って溶媒中の
不純物を吸漬除去する扱者速度及び・汲;d:4量は大
きくなるが、シート化されているために単位体積のシー
ト中に含まれる粉本の含有量が少くない。
In sheet-shaped processed products, the powder is further subdivided, so the specific surface area increases greatly. Therefore, the operator's speed and amount of suction to remove impurities in the solvent increases, but since the sheet is formed into a sheet, the amount of powder contained in a unit volume of sheet is not small.

′f、3図は上記シート状加工品をへ二カム伏に加工し
たものでろって下のシー) 15と上のシート16との
+alに波形のもう1枚のシート14がメジ、該シート
140波形状を山とすると例えばシート15と16の長
さ30菌の間に山の敵を62、山の高さ’に1.9〜2
.2 twとしたハニカム伏加工品17?の体積には細
分化粉末が50〜70y含まれるものとなる。
'f, Figure 3 shows the above sheet-like processed product processed into a diagonal shape (lower sheet).Another corrugated sheet 14 is placed between the sheet 15 and the upper sheet 16. If the 140 wave shape is a mountain, for example, the enemy of the mountain is 62 between the length of sheets 15 and 16 and 30 bacteria, and the height of the mountain is 1.9 to 2.
.. 2 TW honeycomb processed product 17? The volume includes 50 to 70 y of finely divided powder.

本発明では基本的に前記シート加工法又はシートハニカ
ムを遇肖な大きさに切)出しエレメントfヒして使用す
るのである。
In the present invention, basically, the sheet processing method described above or the sheet honeycomb is cut into a suitable size and the elements are used.

シート状加工品を箱に詰めるさいシートそのものを切り
出してこれを槓み上げても艮いが、シートハニカムを丁
度箱と同じ大きさに切シ出して使用しても艮い。シリえ
ば第3図の単一ハニカムを数枚積属ねたハニカムが第4
図でこれを切シ出して使用する。固形体加工品を使用す
る場合と同様にエレメントの数を1薗にする場合、第3
図に示す単一ハニカムを使用する場合と、第4図に示す
積層ね形ハニカムを使用する場合とがある。
When packing a processed sheet product into a box, it is acceptable to cut out the sheet itself and roll it up, but it is also acceptable to cut sheet honeycomb to exactly the same size as the box and use it. In other words, the honeycomb stacked with several single honeycombs shown in Figure 3 is the fourth one.
Cut out and use this in the figure. If the number of elements is one, as in the case of using solid processed products, the third
A single honeycomb as shown in the figure may be used, or a laminated spiral honeycomb as shown in FIG. 4 may be used.

(夫苑例4) 第5図及び第6図はハニカムを円筒形にした場合のクリ
を示すものであり、図囲では外枠を示していないが必要
に応じて外枠を付けることもある。このような使い方に
よると流込んで来る溶媒中の不純物の比重に関しては考
Iぼしないことになるが、第7図に示す如く断商慣に直
角で片側を切捨て、ぞの代シ固形体の加工品17のよう
な誦賢度の加工品をtdめ、溶媒中の不純物の比重が厘
い場合は高M&’部分金下に軽い部分は上に向くように
なして使用する。
(Fuen Example 4) Figures 5 and 6 show the shape of a cylindrical honeycomb, and although the outer frame is not shown in the figure, an outer frame may be attached if necessary. . Using this method does not take into account the specific gravity of impurities in the incoming solvent, but as shown in Figure 7, one side of the solid body is cut off at a right angle, and the other half of the solid body is cut off. If the specific gravity of impurities in the solvent is low, use a processed product with a high degree of recitation, such as Processed Product 17, with the high M&' part facing downward and the light part facing upward.

2次加工品の何れも、夫々れのエレメントに流れ込む浴
媒の過量の制御が天川に於いて大切であり、この制御方
法として第1−〇に下す如き貯留タンク18を用意する
。このさい溶媒は流入口19から流れ込み下部に落ちて
液位が上がる。液位がるる程度のレベルになると流出口
20から、オプション荻1dとした前述の粉末投入タン
クlの流入口21へ流入させるか、又は装置4の流入口
8へ流入させる。ところで貯留タンク18の流入口19
から大量の浴媒が流込み、液位の上昇が早くて流出口2
0からの流量では聞に合わないで液位が点綴位m22ま
で上昇すると警報が鳴シ、更らに液位が上昇すると放流
口23から外へ流出するものとなるのであるが、通常の
設計で貯留タンク18の流出口20VCは流量コントロ
ールパルプ24が設けてあり、従って常時適麓がエレメ
ントに流れることによって設計通りの目的を達成するこ
とのできるものである。
For any of the secondary processed products, it is important at Tenkawa to control the excess amount of bath medium flowing into each element, and as a method for this control, a storage tank 18 as shown in No. 1-0 is prepared. At this time, the solvent flows from the inlet 19 and falls to the bottom, raising the liquid level. When the liquid level reaches a certain level, it is made to flow from the outlet 20 to the inlet 21 of the powder input tank 1 mentioned above as option 1d, or to the inlet 8 of the device 4. By the way, the inlet 19 of the storage tank 18
A large amount of bath medium flows in from the outlet 2, and the liquid level rises quickly.
If the flow rate from 0 is not satisfactory and the liquid level rises to point m22, an alarm will sound, and if the liquid level rises further, it will flow out from the outlet 23, but the normal By design, the outlet 20VC of the storage tank 18 is provided with a flow rate control pulp 24, so that the designed purpose can be achieved by constantly flowing the appropriate amount to the element.

本発明の作用効果は次の笑竣で更らに明らかにされる。The effects of the present invention will be further clarified in the following summary.

来験例1 水50 mgに対しトリクロロエチレン30ダを混合し
た混合液に粉本1gを投入することによって最初のPH
から時間、即ち接触時間と共にどう変化するかを見た。
Experimental Example 1 The initial pH was adjusted by adding 1 g of powder to a mixture of 50 mg of water and 30 da of trichlorethylene.
We looked at how it changes over time, that is, the contact time.

同時にPHの変化時間に対してトリクロロエチレンの除
去がどう変化するかを見た。第8図はその結果を図表に
したもので実8AはPHの変化を、点線はトリクロロエ
チレンの除去量を示す。
At the same time, we looked at how the removal of trichlorethylene changed with the time of pH change. Fig. 8 shows the results in a graph, where Act 8A shows the change in pH and the dotted line shows the amount of trichlorethylene removed.

最初混合液のPHは6.4でめったが、これが8日間で
忌mは増加しアルがり注を示しん。
At first, the pH of the mixed solution was 6.4, but after 8 days the pH increased and showed no signs of corrosion.

同時にこの間にトリクロロエチレンが著しく除去された
。恩赦なPHの上昇は粉末が水の一部を分解し、OHイ
オンの一度を増加さぜるためで、このOHイオンの一部
はゆつくシした反応でトリクロロエチレンの分解に使わ
れる。
At the same time, trichlorethylene was significantly removed during this time. The gradual increase in pH is due to the fact that the powder decomposes some of the water and increases the number of OH ions, and some of these OH ions are used to decompose trichlorethylene in a slow reaction.

接触時間が1週間以上となると、2日以後PHとトリク
ロロエチレンの濃度変化がないま\続いたのが若干変化
が現われるのはこのためである。即ちOHイオンが一部
トリクロロエチレンの分解に、使われるためトリクロロ
エチレン;旙度は減少し、PH値も減少する。
This is why when the contact time is one week or more, the PH and trichlorethylene concentration, which remained unchanged for two days, start to change slightly. That is, since some OH ions are used to decompose trichlorethylene, the trichlorethylene temperature decreases and the pH value also decreases.

央朝例2 ベンジンはヘキサン、へ°ブタンを主成分とするドライ
クリーニングのしみ抜き溶剤として良く使われる。ドラ
イクリーニング工場で繰返して使われると服などの汚れ
を1余去するに従い、ベンジンは赤色を浴び始めピンク
に近くなると洗冴力が低下し使用できなくなる。
Chuocho Example 2 Benzine is often used as a stain removal solvent for dry cleaning, with hexane and hexane as the main ingredients. When benzene is used repeatedly at a dry cleaning factory, as it removes more and more dirt from clothes, it begins to turn red and becomes pink, and its cleaning power decreases, making it unusable.

赤已は主に服などの色素成分を抜きと9、それが溶剤の
中でイオン状態として浴解されるものとなる。
Akami mainly removes pigment components from clothes, etc.9, which is then dissolved in a solvent as an ionic state.

このようにベンジンに不訓物が多゛くなるとPH4直も
低下するので、ベンジンを再生するメントは8面)で各
エレメントに固形体ベンツ) 500 ft″谷3tr
に入れ、・流速を1分間にl−e或は1分間に70−1
にして流し込んだ。
In this way, when there are too many harmful substances in benzene, the PH4 value also decreases, so the number of ment to regenerate benzene is 8) and solid benzene in each element) 500 ft" valley 3tr
- Set the flow rate to l-e per minute or 70-1 per minute.
and poured it.

そして不純物の除去の度合は丙眼で脱色の程度で判断し
同時にPHを測定した。その結果は欠の表の通りである
The degree of removal of impurities was judged by the degree of decolorization using a red eye, and the pH was measured at the same time. The results are shown in the missing table.

表 1 試材:不測物をも・むベンジン 温度:常 温 稜if : 5g1図Bのもの う肉6為9き8ンリ 3 央験例1は水が数量のテトラクロロエチレンで汚染され
た場合のものであるが、本例では純粋なテトラクロロエ
チレンがドライクリニングに使われ、その汚れを除去す
るにつれ、またその間ドライクリーニング禄械部品から
Caイオンを抜き収シ、ブルーの色に盾色された場合に
ついてその赤火とPHi直について行った。装置は夾験
例2と同じ第1図Bのもので:)fJ1エレメントだけ
t通過したものを測定した。この場合の流速は1 jP
Ie/ misでめった。その結果は次表θ通シである
Table 1 Sample material: benzene containing unexpected objects Temperature: room temperature If: 5 g 1 carious tissue in Figure B 6 to 9 x 8 liters 3 Central test example 1 is for the case where water is contaminated with a certain amount of tetrachlorethylene. However, in this example, when pure tetrachlorethylene is used for dry cleaning, and as it removes the dirt, it also extracts Ca ions from the dry cleaning machine parts and is colored blue. I followed Akahi and PHi Nao. The device was the same one shown in Figure 1B as in Experimental Example 2:) Only the fJ1 element passed through t was measured. The flow velocity in this case is 1 jP
I met Ie/mis. The results are shown in the following table θ.

表  2 試験条件 試材:不純物を含むテトラクロロエチレン1M度:常 
濾 装置:第1図Bのもの (発明の幼呆) 本発明は以上の如く実施するものでろって、不純例金含
む水或いは有縁溶剤に対してその不AJB物を汲盾除去
すると共に、水と接;独し触媒的に水分子を分解しOH
イオンJt晶めることによってアルカリ注にする一方、
粉末に含まれる5I02、AezOs   FI2os
ニよつ−Cit 1iiEl展75全減少するように胸
く。便って、不3d ’月は不111B¥//Jを除去
すると同時に薬品を投入せずにPHを調部することので
きるものでめる。
Table 2 Test conditions Sample material: Tetrachlorethylene containing impurities 1M degree: Normal
Filtration device: Fig. 1 B (Baby stage of the invention) The present invention is carried out as described above. , in contact with water; catalytically decomposes water molecules to form OH
While turning it into alkali injection by crystallizing ion Jt,
5I02 contained in powder, AezOs FI2os
Niyotsu-Cit 1ii El Exhibition 75 I feel like the whole thing is decreasing. In short, F3d' month is a device that can remove F111B\//J and at the same time check the pH without adding chemicals.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図A、B、Cは本発明で使用さnる装置の&1.略
図(一部破断図)、第2図はエレメントの−Nを示すも
の、第8図〜第6図はシート伏加工品のレリを示すもの
、第7図は池の例を示すもの。第8はトリクロロエチレ
ンで汚染された水′X友化を示すもので火線は時間に対
するPH変化であシ、点線は同トリクロロエチレンの除
去虚夏化で16゜ l・・・粉本投入タンク 2・・・俟出口3・・・ドレ
ン口 6・・・容品 lO・・・加工品 14.15.16・・・ 5II−自セクション 7・・・堰板 11・・・円面容器 シート18・・・貯留タンク 第 図 第 図 第 図 手 続 r山 正 ilH ・11件の表示 昭和63 年 特 IFI’ 願 第210058号 発明の名称 PHの調節方法 補正をする者 事件との関係 特I「出願人 氏  名(名称) 浅 野 敬 冶 代 理 人 住 所 f7i1山山南1町2番6号 [1陽 ヒ゛ ル
FIGS. 1A, B, and C illustrate &1. of the apparatus used in the present invention. Schematic drawing (partially cutaway), Fig. 2 shows -N of the element, Figs. 8 to 6 show the relief of the sheet-folded product, and Fig. 7 shows an example of the pond. The 8th figure shows the conversion of water contaminated with trichlorethylene, the caustic line is the pH change over time, and the dotted line is the removal of the same trichlorethylene and the temperature rises to 16°l...Powder supply tank 2...・Ball outlet 3...Drain port 6...Container lO...Processed product 14, 15, 16... 5II- Own section 7...Weir plate 11...Circular container sheet 18...・Storage Tank Diagram Diagram Diagram Diagram Procedure r Yamamasa IlH ・Display of 11 cases 1988 Special IFI' Application No. 210058 Name of invention PH adjustment method Name Keiji Asano Agent address f7i1 Yamayamaminami 1-cho 2-6

Claims (12)

【特許請求の範囲】[Claims] (1)金属イオンを吸着した非晶質炭素粒子に金属酸化
物成分を混合した粉末(以下、粉末と称す)を粉末のま
ゝ投入、または2次加工(以下、加工品と称す)し、こ
れを不純物を含む水又は有機溶剤(以下、水を含め溶剤
と称す)に一定時間接触させ、溶媒を浄化すると共に、
PHを中性化するか元の溶媒のPHに回復させることを
特徴としたPHの調節方法。
(1) Powder made by mixing metal oxide components with amorphous carbon particles that have adsorbed metal ions (hereinafter referred to as powder) is introduced as a powder or subjected to secondary processing (hereinafter referred to as processed product), This is brought into contact with water or an organic solvent containing impurities (hereinafter referred to as the solvent including water) for a certain period of time to purify the solvent and
A method for adjusting pH, characterized by neutralizing the pH or restoring it to the original pH of the solvent.
(2)金属イオンはNa、K、Mg、Ca、Cr、Ni
、Mn及びZnを含むことを特徴とする請求項1に記載
のPHの調節方法。
(2) Metal ions are Na, K, Mg, Ca, Cr, Ni
, Mn, and Zn.
(3)金属酸化物はAl_2O_3、SiO_2及びF
e_2O_3を含むことを特徴とした請求項1に記載の
PHの調節方法。
(3) Metal oxides are Al_2O_3, SiO_2 and F
The method for adjusting pH according to claim 1, comprising e_2O_3.
(4)加工品は分散剤又は界面活性剤に分散した液体(
以下、分散液体と称す)、パルプ又は不織布を使用した
シート或はそれをハニカム状などの固形体にしたものを
含むことを特徴とした請求項1に記載のPHの調節方法
(4) Processed products are liquids (
2. The method for adjusting PH according to claim 1, further comprising a sheet using a dispersion liquid (hereinafter referred to as a dispersion liquid), pulp or nonwoven fabric, or a solid body thereof such as a honeycomb shape.
(5)粉末及び分散液体加工品を溶媒中へ直接投入して
攪拌する方法、及び加工品を適量化したエレメントとな
し、このエレメントのまゝ使用する方法を含むことを特
徴とした請求項1に記載のPHの調節方法。
(5) Claim 1, characterized in that it includes a method in which powder and dispersed liquid processed products are directly introduced into a solvent and stirred, and a method in which the processed products are made into an element with an appropriate amount and used as such. PH adjustment method described in .
(6)エレメントは加工品のそれぞれの吸着特性に基づ
き、また溶媒中に含まれる不純物と溶媒との相対比重を
考慮し、加工品入り容器の取付位置又は加工品の詰め方
を決めることを特徴とした請求項5に記載のPHの調節
方法。
(6) The element determines the mounting position of the container containing the processed product or the method of packing the processed product based on the adsorption characteristics of each processed product and considering the relative specific gravity of the impurities contained in the solvent and the solvent. The method for adjusting pH according to claim 5.
(7)固形体加工品を使用する方法として、加工品を箱
形又は円筒形にするか、或いは同形の容器に詰めこれを
このまゝにして溶媒を直接通過させる方法、及び溶媒を
受ける容器を用意し該容器中に上記加工品入りの容器を
入れるか又は取付ける方法として溶媒に含まれる不純物
の比重に従いその取付位置の上下関係を変えるようにな
すことを特徴とした請求項6に記載のPHの調節方法。
(7) Methods for using solid processed products include forming the processed product into a box or cylinder shape, or packing it into a container of the same shape and allowing the solvent to pass through it directly, and a container to receive the solvent. 7. A method according to claim 6, characterized in that the container containing the processed product is placed in or attached to the container by changing the vertical relationship of the attachment position according to the specific gravity of impurities contained in the solvent. How to adjust pH.
(8)シート状の加工品をハニカムとなし、該ハニカム
を横又は縦にして箱又は円筒形の容器に詰め、これを溶
媒に含まれる不純物の比重に従つて溶媒受けの容器に於
ける取付位置の上下関係を変えるようになすことを特徴
とした請求項6に記載のPHの調節方法。
(8) Form a sheet-like processed product into a honeycomb, pack the honeycomb horizontally or vertically into a box or cylindrical container, and install it in a container for receiving a solvent according to the specific gravity of impurities contained in the solvent. 7. The method for adjusting pH according to claim 6, further comprising changing the vertical relationship of the positions.
(9)シートハニカム使用のエレメントを適宜つないで
溶媒の流れが順に各エレメントと接触し、溶媒中のPH
の調節及び不純物を除去することを特徴とした請求項8
に記載のPHの調節方法。
(9) Connect elements using sheet honeycomb as appropriate so that the flow of solvent contacts each element in turn, and the PH in the solvent
Claim 8 characterized in that it adjusts and removes impurities.
PH adjustment method described in .
(10)シートハニカムのエレメントが1個又は2個の
小数の場合、シートハニカムを詰める容器を使用しない
でシートハニカムを円筒形又は角柱形となし、これを支
持する外枠を設け、これに溶媒を流入通過させることを
特徴とした請求項9に記載のPHの調節方法。
(10) When the number of elements in the sheet honeycomb is one or two decimals, the sheet honeycomb is made into a cylindrical or prismatic shape without using a container for packing the sheet honeycomb, an outer frame is provided to support it, and a solvent is attached to the sheet honeycomb. 10. The method for adjusting pH according to claim 9, further comprising the step of flowing and passing through the pH.
(11)シートハニカムが円筒形の場合、その片側を円
筒の円断面に対し直角に切り捨て、その切り捨てた空間
に高密度の他の加工品を詰め、これを外枠又は容器で固
定し溶媒の流れが円断面に直角に流入するようになし、
溶媒中の不純物の比重が溶媒より重い時には高密度部分
が下方となるように、逆の場合は上方となるように取付
けて使用することを特徴とした請求項10に記載のPH
の調節方法。
(11) When the sheet honeycomb is cylindrical, one side of it is cut off at right angles to the circular cross section of the cylinder, the cut out space is filled with other high-density processed products, and this is fixed with an outer frame or container and the solvent is removed. The flow is made to flow at right angles to the circular cross section,
11. The PH according to claim 10, characterized in that when the specific gravity of impurities in the solvent is heavier than the solvent, the high-density part is mounted downward, and in the opposite case, the high-density part is mounted upward.
How to adjust.
(12)シートハニカムを薄い板状のハニカムとなす場
合、これを円筒状に巻上げその円筒状周りに外枠を取付
け、溶媒の流れを円断面へ直角に流すことを特徴とした
請求項10又は11に記載のPHの調節方法。
(12) When the sheet honeycomb is formed into a thin plate-like honeycomb, it is rolled up into a cylindrical shape and an outer frame is attached around the cylindrical shape, so that the solvent flows at right angles to the circular cross section. 12. The method for adjusting pH according to item 11.
JP21005888A 1988-08-23 1988-08-23 Ph control method Pending JPH0259094A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21005888A JPH0259094A (en) 1988-08-23 1988-08-23 Ph control method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21005888A JPH0259094A (en) 1988-08-23 1988-08-23 Ph control method

Publications (1)

Publication Number Publication Date
JPH0259094A true JPH0259094A (en) 1990-02-28

Family

ID=16583118

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21005888A Pending JPH0259094A (en) 1988-08-23 1988-08-23 Ph control method

Country Status (1)

Country Link
JP (1) JPH0259094A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5202044A (en) * 1990-09-12 1993-04-13 Kao Corporation Working fluid composition for refrigerating machine

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5202044A (en) * 1990-09-12 1993-04-13 Kao Corporation Working fluid composition for refrigerating machine

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