JPS5913823A - Incineration of waste ion exchange resin - Google Patents

Incineration of waste ion exchange resin

Info

Publication number
JPS5913823A
JPS5913823A JP12402982A JP12402982A JPS5913823A JP S5913823 A JPS5913823 A JP S5913823A JP 12402982 A JP12402982 A JP 12402982A JP 12402982 A JP12402982 A JP 12402982A JP S5913823 A JPS5913823 A JP S5913823A
Authority
JP
Japan
Prior art keywords
water
ion exchange
exchange resin
oil
emulsion
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
JP12402982A
Other languages
Japanese (ja)
Other versions
JPH0139008B2 (en
Inventor
Takeshi Osada
武 長田
Tadao Yamada
山田 忠男
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.)
Toray Engineering Co Ltd
Original Assignee
Toray Engineering 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 Toray Engineering Co Ltd filed Critical Toray Engineering Co Ltd
Priority to JP12402982A priority Critical patent/JPS5913823A/en
Publication of JPS5913823A publication Critical patent/JPS5913823A/en
Publication of JPH0139008B2 publication Critical patent/JPH0139008B2/ja
Granted legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G5/00Incineration of waste; Incinerator constructions; Details, accessories or control therefor
    • F23G5/02Incineration of waste; Incinerator constructions; Details, accessories or control therefor with pretreatment

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Feeding And Controlling Fuel (AREA)
  • Gasification And Melting Of Waste (AREA)

Abstract

PURPOSE:To dispense with the pre-treatment of waste ion exchange resin such as pulverization of the resin, to incinerate the resin efficiently and to reduce the quantity of resultant exhaust gas by a method wherein the wet and coarse waste ion exchange resin is mixed with fuel oil and water in the presence of an emulsifier to produce oil drop-in-water three component type stabilized emulsion and the emulsion is burned by spraying. CONSTITUTION:Wet and coarse waste ion exchange resin 12 is mixed with fuel oil 10 and water 11 in the presence of emulsifier 13 to thereby produce oil drop- in-water three component type stabilized emulsion. The emulsion thus produced is transferred from a tank 1 through a pump 2 and burned by spraying it into a furnace 4 through a nozzle 3. Further, an auxiliary fuel is supplied through a pump 5 and a nozzle 6.

Description

【発明の詳細な説明】 本発明は廃イオン交換樹脂の焼却処理方法に門出される
湿潤されている粗い廃イオン交換樹脂をそのまま直接、
焼却処理しうる方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention is a method for incinerating waste ion exchange resin, in which the wet coarse waste ion exchange resin is directly processed as it is.
This relates to a method that allows for incineration.

原子力分野などにおいて、そのイオン交換処理工程−か
ら取り出される湿潤されている粗い廃イオン交換樹脂の
発生量の増加が著しく、これの減容化技術の確立が課題
となっており、その−解決策として廃イオン交換樹脂を
焼却処理することが考えられているが、従来のロータリ
ーギルン式、多段炉、流動層炉式、攪拌炉床式などの一
般方法により焼却処理しようとしても、いずれの場合に
おいても燃焼効率が低く、かつ多量の燃焼空気を必要と
するため排ガス処理設備が非常に大型になるという問題
があってこれらの方法は採用し難かった。また他の微粉
炭燃焼のような方式により焼却処理しようとしても。
In the nuclear power field, etc., the amount of wet coarse waste ion exchange resin extracted from the ion exchange treatment process has increased significantly, and the establishment of technology to reduce its volume has become an issue. However, even if conventional methods such as rotary gill, multi-stage furnace, fluidized bed furnace, and stirred hearth furnace are used to incinerate waste ion exchange resin, it will not work. However, these methods had low combustion efficiency and required a large amount of combustion air, making the exhaust gas treatment equipment extremely large, making it difficult to adopt these methods. Even if you try to incinerate it using other methods such as pulverized coal combustion.

湿潤されている粗い廃イオン交換樹脂を前処理として2
00メツシユ以下に倣粉砕し所定に乾燥させなければな
らなく、而してその設備が複雑になると共に粉じん爆発
に対する高度な技1ホi的7・1策も必要とされるとい
うような問題があってこの方法も採用し難かった。
2 as a pretreatment of wetted coarse waste ion exchange resin.
It is necessary to crush the powder to a size of 0.00 mesh or less and dry it in a specified manner, which makes the equipment complex and requires sophisticated techniques and 7/1 measures to prevent dust explosions. This method was also difficult to adopt.

本発明はこのような従来の問題点に鑑みて発明されたも
のであり、りその目的とするところは。
The present invention was invented in view of such conventional problems, and its purpose is to:

イオン交換処理工程から取り出される湿潤されている粗
い廃イオン交換樹脂をそのまま焼却。
The wet coarse waste ion exchange resin extracted from the ion exchange treatment process is directly incinerated.

すなわち微粉砕や乾燥などの前処理を−切しなくても前
記樹脂を効率よく焼却し得て、かつそのυ1゛ガス量を
より一段と減らすことができる廃イオン交換樹脂の焼却
処理方法を提供しようとするにある。
In other words, we would like to provide a method for incinerating waste ion exchange resin that can efficiently incinerate the resin without performing pretreatment such as pulverization or drying, and further reduce the amount of υ1゛ gas. There it is.

この目的を達成する本発明に係る廃イオン交換樹脂の焼
却処理方法は、湿潤されている粗い廃イオン交換樹脂を
机下剤の存在下で燃料油及び水と混合して水中油滴型得
3成分系の安定なエマルジョンとし1次いでこれを単独
機または助燃焼土で噴霧燃焼させることを特徴とするも
のである。
The method for incineration of waste ion exchange resin according to the present invention which achieves this objective is to mix the moistened coarse waste ion exchange resin with fuel oil and water in the presence of a laxative to obtain a three-component oil-in-water type product. The system is characterized by forming a stable emulsion and then spraying and burning this in a single machine or in auxiliary combustion soil.

イオン交換処理工程から取り出される廃イオン交換樹脂
は粗い樹脂であって、かつ湿潤されておジ、これを燃料
油または水のみと混合しても安定な均一分散体を得るこ
とが困難であるが。
The waste ion exchange resin taken out from the ion exchange treatment process is a coarse resin and is wet, so it is difficult to obtain a stable homogeneous dispersion even if it is mixed with fuel oil or water alone. .

本発明においては前記廃イオン交換樹脂を乳化剤の存在
下で燃料油及び水と混合するので廃イオン交換樹脂−燃
料油−yJ< 3成分系の甑めて安定な水中油滴型エマ
ルジョンが得られる。
In the present invention, since the waste ion exchange resin is mixed with fuel oil and water in the presence of an emulsifier, a stable oil-in-water emulsion with a 3-component system of waste ion exchange resin - fuel oil - yJ < is obtained. .

なお前記廃イオン交換樹脂を油中水滴型乳化剤の存在下
で燃料油及び水と混合すれば油中水滴型エマルシコンも
得ることができるが、この油中水滴型エマルジョンでは
本発明の目的をより十分に達成することが困難である。
Note that a water-in-oil emulsion can also be obtained by mixing the waste ion exchange resin with fuel oil and water in the presence of a water-in-oil emulsifier; difficult to achieve.

なぜならばこノ種のエマルジョンは燃料油に対し水のi
t増すと常温での流動性が悪化して送液操作が困難にな
り、!、た湿潤されている粗い廃イオン交換樹脂と混合
液(燃料油と水とを混合した液)との重量比が大きくな
るにつれても流動性が悪化するためである。
This is because this type of emulsion has a high concentration of water compared to fuel oil.
If t increases, the fluidity at room temperature will deteriorate and the liquid feeding operation will become difficult. This is because fluidity deteriorates as the weight ratio of the wetted coarse waste ion exchange resin and the mixed liquid (liquid mixed with fuel oil and water) increases.

本発明において水中油滴型エマルジョンの組成範囲は特
に限定されないが、燃料油と水との重量比が70 :3
0〜20:80で、かつ廃イオン交換樹脂と混合液(燃
料油と水とを混合した液)との重量比が20:80〜7
0:30であるのが(1fましい。
In the present invention, the composition range of the oil-in-water emulsion is not particularly limited, but the weight ratio of fuel oil and water is 70:3.
0 to 20:80, and the weight ratio of waste ion exchange resin to mixed liquid (liquid mixed with fuel oil and water) is 20:80 to 7.
0:30 is (1f).

表1において各種組成範囲の水中油滴型エマルジョンの
実施例を示す。なお同表中における(A)〜(F) 、
 (0/W) 、 (R/L)は下記全それぞれ表わし
ていると共に「乳濁安定性」の行における(・記す−は
良好を、・:△)記号は1時間以内で分離を、(う記号
は数分で分離をそれぞれを表わしており。
Table 1 shows examples of oil-in-water emulsions having various composition ranges. In addition, (A) to (F) in the same table,
(0/W) and (R/L) represent all of the following, and in the row of "emulsion stability" (・marked - means good, ・:△) sign means separation within 1 hour, ( The symbols represent each separation in minutes.

さらに「常温流動性」の行におけるC1)記号は良好を
、そして(Δ)記号は不良を表わしている。
Furthermore, the C1) symbol in the "room temperature fluidity" row indicates good quality, and the (Δ) symbol indicates poor quality.

なお本実施例においては水中油滴型ノニオン系の乳化剤
を使用している。
In this example, an oil-in-water type nonionic emulsifier is used.

(A) : 60〜400メソシユで空隙率が7.6チ
の湿潤されている廃カチオン交換樹脂(オルガノ株式会
社製のパウデックスPCH)。
(A): A wetted waste cation exchange resin (Powdex PCH manufactured by Organo Co., Ltd.) with a porosity of 60 to 400 mS and a porosity of 7.6 h.

(B) : 60〜400メツシユで空隙率が31チの
湿潤されている廃アニオン交換樹脂(オルガノ株式%式
%) (C):有効径が0.450.60mmで空隙率が35
チの湿潤されている廃カチオン交換樹脂(オルガノ株式
会社製のアンバーライトlR120B)。
(B): Wetted waste anion exchange resin with a mesh size of 60 to 400 and a porosity of 31 inches (organo stock% formula %) (C): Effective diameter of 0.450.60 mm and a porosity of 35
The waste cation exchange resin (Amberlite 1R120B manufactured by Organo Co., Ltd.) was wetted with water.

(D):有効径が0 、45−0 、6 Q ynmで
空隙率が35qbの湿潤されている廃アニオン交換樹脂
(オルガノ株式会社製のアンバーライトIRA400)
(D): Wetted waste anion exchange resin with an effective diameter of 0, 45-0, 6 Q ynm and a porosity of 35 qb (Amberlite IRA400 manufactured by Organo Co., Ltd.)
.

(E):前記(A)と(B)との混合物であって、nJ
記iA)とCB)との重量比が3:1のもの。
(E): A mixture of the above (A) and (B), with nJ
The weight ratio of iA) and CB) is 3:1.

(F):前記(A)〜(D)の混合物であって、前記i
A)と(B)と(C)と(D)との重量比が6:2:2
:lのもの。
(F): A mixture of the above (A) to (D), wherein the above i
The weight ratio of A), (B), (C) and (D) is 6:2:2
:l's.

(0/W) :燃料油と水との重量比。(0/W): Weight ratio of fuel oil and water.

(R/L) :前記(A)〜(F)の廃イオン交換樹脂
それぞれと混合液(燃料油と水とを混合したgl)と0
重量比・          //表  1 (水中油滴型エマルジョン) このように本発明においては水中油滴型エマルジョンの
組成範囲を各種に設けることができるが、実施例7及び
9のような組成範囲に設けるのはあまり好ましくない。
(R/L): Each of the waste ion exchange resins (A) to (F) above and a mixed liquid (gl of fuel oil and water mixed) and 0
Weight ratio // Table 1 (Oil-in-water emulsion) As described above, in the present invention, the oil-in-water emulsion can be provided in various composition ranges, but the composition ranges as in Examples 7 and 9 are I don't really like that.

すなわち実施例7のように(o/W)を(16/84)
に設けると、乳濁安定性及び常温流動性が良好であって
もこれを燃焼する際、助燃焼下で燃焼させても火炎の安
定性が不十分となり、また実施例9のように(0/W)
を(85/15)に設けると流動性が悪化して送液操作
が困難となるからあまり好ましくない。
That is, as in Example 7, (o/W) is (16/84)
If the emulsion stability and room temperature fluidity are good, the flame stability will be insufficient even if it is burned under auxiliary combustion, and as in Example 9, the flame stability will be insufficient. /W)
(85/15) is not very preferable because the fluidity deteriorates and the liquid feeding operation becomes difficult.

なお(0/W )に関し一般に少なくとも(10/90
)以上に設ければ安定した乳濁性が得られ、この場合に
おける油滴は数ミクロンから数十ミクロンになって水中
に高密度に分散して樹脂粒子の沈降を防止しうるが、燃
焼に際して安定な火炎を得るためには助燃焼下でも(2
0/80)以」二に設けるのが好ましい。
Regarding (0/W), generally at least (10/90
) or above, stable emulsification can be obtained, and in this case, the oil droplets will be from several microns to several tens of microns in size and dispersed in water at a high density, preventing the resin particles from settling. In order to obtain a stable flame, even under auxiliary combustion (2
0/80) or less is preferable.

また( R/L )についてはこれをあまり大きくする
と流動性が悪化して送液操作が困難となるがら(70/
30)以下が好ましい。
Regarding (R/L), if it is too large, the fluidity will deteriorate and the liquid feeding operation will be difficult; however, (70/L)
30) The following are preferred.

次に表2において各種組成範囲の油中水滴型エマルジョ
ンを示す。なおこの表中における(A1−(F) 、 
(0/W) 、 (R/L:) 、その池各種記号は表
1におけるそれと同じもの表わし、乳化剤は油中水滴型
ノニオン系のものが用いられている。
Next, Table 2 shows water-in-oil emulsions having various composition ranges. In this table, (A1-(F),
(0/W), (R/L:), the various symbols for the pond are the same as those in Table 1, and the emulsifier used is a water-in-oil type nonionic emulsifier.

表  2 (油中水滴型エマルジョン) これからして明らかのように油中水滴型エマルジョンは
表1に示される水中油滴型エマルジョンに比して流動性
が著しく劣っており、また(R/L)をあまり上げられ
ず、廃イオン交換樹脂当りの燃料油使用量が多くなり、
従って油中水滴型エマルジョンでは本発明の目的をより
十分に達成し得ないことがわかる。
Table 2 (Water-in-oil emulsion) As is clear from this, the water-in-oil emulsion is significantly inferior in fluidity to the oil-in-water emulsion shown in Table 1, and (R/L) The amount of fuel oil used per waste ion exchange resin increases.
Therefore, it can be seen that the objects of the present invention cannot be more fully achieved with water-in-oil emulsions.

なお表3において水または軽油のどちらか一方及び乳化
剤を添加しない場合の例を示すが、ここにおける(R/
W)は前記樹脂(F)と水との重量比を、また(R10
)は前記樹脂(F)と軽油との重量比を表わしている。
Table 3 shows an example where either water or light oil and no emulsifier are added;
W) is the weight ratio of the resin (F) and water, and (R10
) represents the weight ratio of the resin (F) and light oil.

表  3 (水または軽油のどちらか一方及び乳化剤を添加しない
エマルジョン)この例によれば乳濁安定性が十分でない
のでこのエマルジョンを使用しても本発明の目的を達成
し得ないことは述べる寸でもなく明らかである。
Table 3 (Emulsion without the addition of either water or diesel oil and an emulsifier) According to this example, the emulsion stability is insufficient, so it can be stated that even if this emulsion is used, the object of the present invention cannot be achieved. But it's obvious.

なお」二連の実施例においては燃料油として軽油音用い
ているが1本発明においてはこ呪芹定されず重油、溶油
、廃油、廃溶剤などを用いてもよい。
Note that in the two embodiments, light oil is used as the fuel oil, but in the present invention, this is not limited, and heavy oil, molten oil, waste oil, waste solvent, etc. may also be used.

また乳化剤はノニオン型界面活性剤が好ましく。Further, the emulsifier is preferably a nonionic surfactant.

カチオン及びアニオン型活性剤を用いると廃イオン交換
樹脂と反応して乳化能力を低下させて長期間安定な乳濁
性を維持し難い。
When cationic and anionic activators are used, they react with the waste ion exchange resin and reduce the emulsifying ability, making it difficult to maintain stable emulsifying properties for a long period of time.

本発明においては上述したように、湿潤されている粗い
廃イオン交換樹脂を乳化剤の存在下で?CrA油及び水
と混合して水中油滴型の3成分系の安定なエマルジョン
を生成するが1次いでこれを噴M燃焼させるのである。
In the present invention, as described above, the coarse waste ion exchange resin is wetted in the presence of an emulsifier. It is mixed with CrA oil and water to form a stable three-component emulsion in the form of oil-in-water droplets, which is then combusted.

すなわち第11iの燃焼系統図において示すように、槽
(1)から水中油滴型エマルジョンをポンプ(2)ヲ介
して送液してノズル(3)から炉(4)内へ噴霧し燃焼
させる。
That is, as shown in the combustion system diagram No. 11i, the oil-in-water emulsion is sent from the tank (1) through the pump (2), and is sprayed into the furnace (4) through the nozzle (3) and combusted.

なおこの際、助燃焼土で噴霧燃焼させるのが好ましい。At this time, it is preferable to carry out spray combustion using auxiliary combustion soil.

図示の装置においてはポンプ(5)、ノズル(6)ヲ配
した助燃油供給管路を設けている。なお(7)は燃焼用
エアーを送気するブロアー、(8)は噴霧用の加圧空気
を送気するコンブレノザー。
The illustrated apparatus is provided with an auxiliary fuel oil supply conduit in which a pump (5) and a nozzle (6) are arranged. Note that (7) is a blower that sends combustion air, and (8) is a comb noser that sends pressurized air for spraying.

(9)は乳化器、00)は燃料油供給管路、 (1,1
)は水供給管路、02は湿潤されている粗い廃イオン交
換樹脂を供給する管路、αjは乳化剤供給管路全それぞ
れ示している。
(9) is an emulsifier, 00) is a fuel oil supply pipe, (1,1
) indicates a water supply pipe, 02 indicates a pipe supplying wetted coarse waste ion exchange resin, and αj indicates all emulsifier supply pipes.

而してこのようにして廃イオン交換樹脂を焼却処理する
ことにより油中水滴型エマルジョンの場合に比して各種
のすぐれた効果が得られる。
By incinerating the waste ion exchange resin in this manner, various superior effects can be obtained compared to the case of water-in-oil emulsion.

すなわちそのlとして、水添加量を多くすればエマルジ
ョンの粘度が低下する(油中水滴型の場合は高くなる)
から2排ガス温度を所定にさげる際に水添加量を容易に
増加させることができ07゛す る云細チ誼C燃焼空気量を最低に維持することができる
という効果が得られる。
In other words, if the amount of water added is increased, the viscosity of the emulsion will decrease (in the case of water-in-oil type, it will increase).
Therefore, when lowering the exhaust gas temperature to a predetermined level, the amount of water added can be easily increased, and the effect is that the amount of combustion air can be maintained at a minimum.

またその2として、廃イオン交換樹脂量当りの燃料使用
量を少なくすることができるという効果が得られ、更に
その3として、C重油などの高粘度油を使用する場合に
おいてもエマルジョン粘度は連続相である水の粘度に収
れんするので常温で噴霧可能な流動性が得られるという
効果、更にまたその4として、エマルジョンが流動して
も静電気の蓄積がないのでこれによる気相部の着火爆発
の恐れがな−い(油中水滴型の場合は危険性が犬)とい
う効果が得られる。
Secondly, the amount of fuel used per amount of waste ion exchange resin can be reduced, and thirdly, even when using high viscosity oil such as C heavy oil, the viscosity of the emulsion is reduced by the continuous phase. Since the viscosity of water converges to a certain level, fluidity that can be sprayed at room temperature can be obtained.Fourthly, even if the emulsion flows, there is no accumulation of static electricity, so there is a risk of ignition and explosion in the gas phase. (In the case of water-in-oil type, it is dangerous).

次に第4図において各種の水中油滴型エマルジョン全第
1図の装置によV燃焼させた実施例を示す。なお同表中
における(F) 、 (0/W) 、 (R/L)は前
述したそれと同じものを示している。
Next, FIG. 4 shows an example in which various oil-in-water emulsions were subjected to V-combustion using the apparatus shown in FIG. 1. Note that (F), (0/W), and (R/L) in the same table indicate the same as those described above.

表  4 (水中油滴型エマルジョンの焼却) このように本発明によれば湿潤されている粗い廃イオン
交換樹脂全良好に焼却処理することができる。なお灯油
と軽油については(0/W) 。
Table 4 (Incineration of oil-in-water emulsion) As described above, according to the present invention, all wetted coarse waste ion exchange resin can be incinerated in a satisfactory manner. For kerosene and diesel oil (0/W).

(R/L) を同一にする限りその乳濁安定性及び常温
流動性がほぼ同じであった。
As long as (R/L) was the same, the emulsion stability and room temperature fluidity were almost the same.

以上、詳述したように本発明によれば各種のすぐれた効
果が得られるが、ここでさらに詳述するに、その1とし
て、完全燃焼を容易化して排ガス量を少なくしうという
効果が得られる。すなわち廃イオン交換樹脂処理量当り
の排ガス量を少なくするためには前記樹脂を液体焼判化
して燃焼空気量を理論燃焼空気比に近づけることが望ま
しく、また前記樹脂を完全燃焼させるには出来る限り高
温帯を通過させることが必要であるが9本発明において
は前記樹脂を燃料油などと混合して液体燃料として取扱
えるような流動性が良く、かつ安定な均一分散液とし、
これを噴霧燃焼させている。而して前記樹脂が必ず高温
度の火炎を通過するからその燃焼を効率よく行うことが
できるので完全燃焼が達成できる。
As detailed above, various excellent effects can be obtained according to the present invention.To explain in more detail here, one of them is that it facilitates complete combustion and reduces the amount of exhaust gas. It will be done. In other words, in order to reduce the amount of exhaust gas per amount of waste ion exchange resin processed, it is desirable to make the amount of combustion air close to the theoretical combustion air ratio by liquid burning the resin, and to burn the resin completely, as much as possible. Although it is necessary to pass through a high temperature zone, 9 In the present invention, the resin is mixed with fuel oil etc. to form a stable uniform dispersion with good fluidity that can be handled as a liquid fuel,
This is sprayed and burned. Since the resin always passes through the high-temperature flame, its combustion can be carried out efficiently and complete combustion can be achieved.

次にその2として、燃料を節減しうると共にNOxも減
らすことができるという効果が15)られる。すなわち
エマルジョンの均一分散性を安定に維持出来れば定常な
噴霧燃焼を保つことができて前記樹脂の着火を安定しう
るので完全燃焼に必要な炉内温度全過度に高くする必要
はない。
Secondly, there is an effect that fuel can be saved and NOx can also be reduced15). That is, if the uniform dispersion of the emulsion can be stably maintained, steady spray combustion can be maintained and the ignition of the resin can be stabilized, so there is no need to raise the total temperature in the furnace excessively, which is necessary for complete combustion.

一般の焼却処理では炉内温度が過度に高くなった場合に
は燃焼空気量全増加させて温度を下げる方法が採られて
いるが1本発明においては含廃樹脂エマルジョンの発熱
量は水の添加量を変えることにより容易に調整出来るの
で、燃焼空気量全理論空気量の近くに保持したままで炉
内温度の過度上昇防止を主に(0/W )の変更で容易
に行うことができる。また( 0/W )が小さく、前
記エマルジョンの発熱量が低い場合に助燃焼土で噴霧燃
焼を行うので、炉内温度の調nを助燃焼用燃料のコント
ロールで行うことができる。
In general incineration treatment, when the temperature inside the furnace becomes excessively high, a method is adopted in which the total amount of combustion air is increased to lower the temperature, but in the present invention, the calorific value of the waste resin emulsion is reduced by adding water. Since it can be easily adjusted by changing the amount, it is possible to prevent an excessive rise in the furnace temperature while maintaining the combustion air amount close to the total theoretical air amount, mainly by changing (0/W). Furthermore, when (0/W) is small and the calorific value of the emulsion is low, spray combustion is performed with the auxiliary combustion soil, so that the temperature inside the furnace can be adjusted by controlling the auxiliary combustion fuel.

なお水の添加は炉内温度の過度な上昇防止及び燃焼炎温
度分布の均一化の両面からNOx低減化に大きく貢献し
ている。また廃イオン交換樹脂当りの使用燃料は出来る
だけ少ないことが望ましいが、油中水滴型エマルジョン
では表2の比較例で明らかのとと< (0/W) ’&
下げるかまたけ(R/L)ffi上げると流動性が悪化
して安定な噴霧燃焼が得難い。これに苅し本発明に係る
水中油滴型エマルジョン(でおいては(R/L)が(6
0/40)でも完全燃焼が容易であり、従って燃料使用
欧の節減が図れる、 次にその3として、微粉砕及び乾燥などの前処理を省く
ことができるという効果が得られる。
Note that the addition of water greatly contributes to reducing NOx by preventing an excessive rise in the temperature inside the furnace and making the combustion flame temperature distribution uniform. In addition, it is desirable to use as little fuel as possible per waste ion exchange resin, but in water-in-oil emulsions, it is clear from the comparative example in Table 2 that < (0/W) '&
If it is lowered or increased (R/L)ffi, the fluidity deteriorates and it is difficult to obtain stable spray combustion. The oil-in-water emulsion according to the present invention (in which (R/L) is (6
0/40), complete combustion is easy, and therefore fuel consumption can be reduced. Thirdly, pretreatment such as pulverization and drying can be omitted.

f19’のイオン交換樹脂はスチレン−ジビニルベンゼ
ンの架橋型共重合体など全基本購成物とした熱硬化性の
高分子物質であり、かつ廃イオン交換樹脂粒の内部には
多量の水が包含されてこれの乾燥速度は極めて遅い。し
かしながら本発明においては水中油滴型エマルジョンを
噴霧燃焼させて必ず高温の燃焼炎にしうるので1粒子径
が1M程度の廃イオン交換樹脂でも火炎中で破砕して微
細化することができる。
The ion exchange resin of f19' is a thermosetting polymer material such as a crosslinked copolymer of styrene and divinylbenzene, and a large amount of water is contained inside the waste ion exchange resin particles. However, the drying speed is extremely slow. However, in the present invention, since the oil-in-water emulsion can be spray-combusted to produce a high-temperature combustion flame, even waste ion exchange resin having a particle size of about 1M can be crushed in the flame and made into fine particles.

すなわち燃焼時においては樹脂粒子内包含水の逸散速度
より粒子内への加熱速度がはやくなり。
That is, during combustion, the rate of heating into the particles becomes faster than the rate of escape of the water contained within the resin particles.

粒子は内部の水蒸気圧により破砕される。而して前処理
しなくても完全燃焼させることができる。なお第1図に
示される装置における乳化器(9)は振動式、攪拌式、
乱流混合式、噴射式、衝撃式、超音波式など各種型式に
設けることができ、また炉(4)も横型、竪型の噴霧燃
焼炉その他サイクロン式燃焼炉に設けることができる。
Particles are crushed by internal water vapor pressure. Thus, complete combustion can be achieved without pretreatment. The emulsifier (9) in the apparatus shown in FIG. 1 may be of a vibration type, a stirring type, or
It can be provided in various types such as a turbulent mixing type, an injection type, an impact type, and an ultrasonic type, and the furnace (4) can also be installed in a horizontal type, a vertical type spray combustion furnace, or a cyclone type combustion furnace.

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

第1図は本発明の実施例を示し、廃イオン交換樹脂の焼
却処理装置の概略構成図である。 (1):エマルジョン化槽    (4):炉00):
燃料油供給管路     (1υ:水供給管路θの:廃
イオン交換樹脂供給管路 0:):乳化剤供給管路 特許出願人 東V・エンジニアリング株式会社1、
FIG. 1 shows an embodiment of the present invention, and is a schematic diagram of a waste ion exchange resin incineration treatment apparatus. (1): Emulsion tank (4): Furnace 00):
Fuel oil supply pipe (1υ: Water supply pipe θ: Waste ion exchange resin supply pipe 0:): Emulsifier supply pipe Patent applicant ToV Engineering Co., Ltd. 1,

Claims (2)

【特許請求の範囲】[Claims] (1)湿潤されている粗い廃イオン交換樹脂全乳化剤の
存在下で燃料油及び水と混合して水中油滴型3成分系の
安定なエマルジョンとし。 次いでこれ全単独または助燃焼下で噴霧燃焼させること
を特徴とする廃イオン交換樹脂の焼却処理方法。
(1) Coarse waste ion exchange resin that has been moistened is mixed with fuel oil and water in the presence of an emulsifier to form a stable oil-in-water three-component emulsion. A method for incineration of waste ion exchange resin, characterized in that the resin is then spray-combusted either alone or with auxiliary combustion.
(2)  エマルジョンの組成範囲が、燃料油と水との
重量比が70:30〜20:80で、かつ廃イオン交換
樹脂と燃料油及び水の混合液との重量比が20:80〜
70:30であること全特徴とする特FT’請求の範囲
(1)に記載の廃イオン交換樹脂の焼却処理方法。
(2) The composition range of the emulsion is such that the weight ratio of fuel oil to water is 70:30 to 20:80, and the weight ratio of waste ion exchange resin to the mixture of fuel oil and water is 20:80 to 20:80.
The method for incinerating waste ion exchange resin according to claim (1), characterized in that the ratio is 70:30.
JP12402982A 1982-07-15 1982-07-15 Incineration of waste ion exchange resin Granted JPS5913823A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12402982A JPS5913823A (en) 1982-07-15 1982-07-15 Incineration of waste ion exchange resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12402982A JPS5913823A (en) 1982-07-15 1982-07-15 Incineration of waste ion exchange resin

Publications (2)

Publication Number Publication Date
JPS5913823A true JPS5913823A (en) 1984-01-24
JPH0139008B2 JPH0139008B2 (en) 1989-08-17

Family

ID=14875264

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12402982A Granted JPS5913823A (en) 1982-07-15 1982-07-15 Incineration of waste ion exchange resin

Country Status (1)

Country Link
JP (1) JPS5913823A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59177148U (en) * 1983-05-13 1984-11-27 オムロン株式会社 timer variable resistor
JPS61253498A (en) * 1985-05-02 1986-11-11 三菱重工業株式会社 Method of processing spent ion exchange resin
FR2679319A1 (en) * 1991-07-15 1993-01-22 Gradient Rech Royallieu PROCESS FOR THE INCINERATION OF ORGANIC WASTE.
FR2691524A1 (en) * 1992-05-20 1993-11-26 Servithen Sarl Disposal of radioactive graphite without contaminating environment - by pulverising, mixing with water and burning, then purifying combustion gases and recycling unburnt solids
JP2002115835A (en) * 2000-10-06 2002-04-19 Nakanishi Giken:Kk Process for decomposition of organic chlorine compound
JP2007199023A (en) * 2006-01-30 2007-08-09 Toshiba Corp Ion-exchange resin processing method, ion-exchange resin pulverizing system, decontamination apparatus, nuclear power station, decontamination apparatus modifying method and nuclear power station modifying method
CN102230628A (en) * 2011-04-22 2011-11-02 马鞍山钢铁股份有限公司 Innocent treatment method for waste ion exchange resin

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59177148U (en) * 1983-05-13 1984-11-27 オムロン株式会社 timer variable resistor
JPS61253498A (en) * 1985-05-02 1986-11-11 三菱重工業株式会社 Method of processing spent ion exchange resin
FR2679319A1 (en) * 1991-07-15 1993-01-22 Gradient Rech Royallieu PROCESS FOR THE INCINERATION OF ORGANIC WASTE.
FR2691524A1 (en) * 1992-05-20 1993-11-26 Servithen Sarl Disposal of radioactive graphite without contaminating environment - by pulverising, mixing with water and burning, then purifying combustion gases and recycling unburnt solids
JP2002115835A (en) * 2000-10-06 2002-04-19 Nakanishi Giken:Kk Process for decomposition of organic chlorine compound
JP2007199023A (en) * 2006-01-30 2007-08-09 Toshiba Corp Ion-exchange resin processing method, ion-exchange resin pulverizing system, decontamination apparatus, nuclear power station, decontamination apparatus modifying method and nuclear power station modifying method
JP4679377B2 (en) * 2006-01-30 2011-04-27 株式会社東芝 Ion exchange resin treatment method, ion exchange resin atomization system, decontamination equipment, nuclear power plant, decontamination equipment modification method, and nuclear power plant modification method
CN102230628A (en) * 2011-04-22 2011-11-02 马鞍山钢铁股份有限公司 Innocent treatment method for waste ion exchange resin

Also Published As

Publication number Publication date
JPH0139008B2 (en) 1989-08-17

Similar Documents

Publication Publication Date Title
US3958915A (en) Method of burning emulsion oils
CN202199276U (en) Fuel oil emulsifying device
DE2459040A1 (en) ATOMIZATION PROCESS
US5513583A (en) Coal water slurry burner assembly
JPS5913823A (en) Incineration of waste ion exchange resin
US3738289A (en) Counter-flow sludge burner
EP0581230A2 (en) Activated, ionized fuel and apparatus for producing the same as well as combustion system for the same
JP2001522979A (en) Fuel combustion method and combustion reactor
US5816790A (en) Heavy oil emulsified fuel combustion equipment
CN1109735C (en) Oil-water-coal slurry and its preparing process
JP3458262B2 (en) Heavy oil combustion method and apparatus used therefor
KR20070096450A (en) Emulsion combustion apparatus
JP2000144158A (en) Water-oil mix fuel and its production
US4151259A (en) Use of oil-water emulsions in a hydrothermal process
US3089539A (en) Method and fuel for operating combustion equipment
JP2006112666A (en) Combustion device provided with emulsified fuel supply system
CN101007970A (en) Heavy oil modified fuel oil for substituting for heavy diesel oil and its production method
JPH11140470A (en) Water-fossil fuel mixed emulsion
KR910006270B1 (en) Method of combustion
JPS60231794A (en) Improving quality of low-grade oil
JPS6046332B2 (en) Atomization method for liquid fuel, etc.
JPS62138609A (en) Heavy oil burning method
JPH01179814A (en) Manufacture of fuel oil mixed with air and water and its manufacturing device
CN103939891A (en) Turbulence intensified combustion method and combustion device of water-coal-slurry
JPS6082706A (en) Combustion method for heavy oil mixed with water