JP2000282155A - Lead separating method - Google Patents

Lead separating method

Info

Publication number
JP2000282155A
JP2000282155A JP9345599A JP9345599A JP2000282155A JP 2000282155 A JP2000282155 A JP 2000282155A JP 9345599 A JP9345599 A JP 9345599A JP 9345599 A JP9345599 A JP 9345599A JP 2000282155 A JP2000282155 A JP 2000282155A
Authority
JP
Japan
Prior art keywords
lead
chlorine
chloride
compound
ratio
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
JP9345599A
Other languages
Japanese (ja)
Inventor
Koichiro Sato
宏一郎 佐藤
Yasushi Yamamoto
泰史 山本
Taku Nakano
卓 中野
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.)
Taiheiyo Cement Corp
Original Assignee
Taiheiyo Cement Corp
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 Taiheiyo Cement Corp filed Critical Taiheiyo Cement Corp
Priority to JP9345599A priority Critical patent/JP2000282155A/en
Publication of JP2000282155A publication Critical patent/JP2000282155A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

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  • Manufacture And Refinement Of Metals (AREA)

Abstract

PROBLEM TO BE SOLVED: To make usable wastes as a raw material of cement with reduced residual ratio of the lead contained therein by baking wastes, etc., to be treated at a temperature above the boiling point of lead chloride in the presence of chlorine of a quantity balanced with the total content of the lead compound and the alkaline metal compound. SOLUTION: Material to be treated containing lead compound such as residential and industrial wastes are baked at a temperature above the boiling point of lead chloride (about 950 deg.C) in the presence of chlorine, and the lead compound is vaporized and separated as lead chloride to reduce the lead content. The quantity of chlorine is balanced with the total content of the lead compound and the alkaline metal compound in the material to be treated. For example, the baking temperature of 950-1500 deg.C is preferable when the chlorine equivalent ratio A=(Cl-R)/Pb (Cl, R and Pb denote the chemical equivalent of chlorine, alkaline metal and lead, respectively) is >=-10, and further, the temperature is preferably 1,400-1,500 deg.C when A is between -10 and -5, and >=950 deg.C when A is >=-5. The residual ratio of lead contained in the wastes is <= about 20 wt.%, preferably <= about 3%.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は廃棄物等から鉛を効
率よく分離して鉛の残留率を大幅に低減する方法に関す
る。より詳しくは、生活・産業廃棄物に含まれる鉛の残
留率を20wt%以下、好ましくは10wt%以下に分離し
てセメント原料として利用できるようにする鉛の分離方
法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for efficiently separating lead from wastes and the like to greatly reduce the residual ratio of lead. More specifically, the present invention relates to a method for separating lead in which the residual ratio of lead contained in domestic and industrial wastes is reduced to 20% by weight or less, preferably 10% by weight or less, so that the lead can be used as a raw material for cement.

【0002】[0002]

【従来の技術】近年、都市ゴミ焼却灰、下水汚泥焼却灰
やその溶融スラグおよびこれらの飛灰などの廃棄物量が
著しく増加し、その処理対策が問題となっている。これ
らの廃棄物の処理対策として、含有する金属化合物を回
収し、またその焼却物をセメント原料として利用する試
みがなされている。この焼却物には廃棄物に由来するか
なりの量の鉛化合物が含まれており、これを効率よく分
離する必要がある。
2. Description of the Related Art In recent years, the amount of waste such as incinerated ash from municipal waste, incinerated ash from sewage sludge, its molten slag, and fly ash has been remarkably increased. As a disposal measure of these wastes, attempts have been made to recover contained metal compounds and use the incinerated materials as cement raw materials. This incinerated material contains a considerable amount of lead compounds derived from wastes, and it is necessary to separate this efficiently.

【0003】[0003]

【発明が解決しようとする課題】廃棄物中に含まれる鉛
は塩素の存在下で焼成することにより、塩化鉛に転じて
揮発させることができる。しかし、アルカリ金属が共存
すると鉛の塩素化による揮発が抑制されて十分に鉛を分
離できない問題がある。アルカリ金属塩化物と塩化鉛の
蒸気圧を比較すると、塩化鉛の蒸気圧が低いので、従来
はアルカリ金属の存在は鉛の揮発に影響しないと一般に
考えられているが、実際にはアルカリ金属の方が鉛より
も塩化物となる傾向が強いため、鉛とアルカリ金属が共
存すると、アルカリ金属によって塩化鉛の一部が酸化鉛
に転換されて鉛の揮発が抑制される。このため、酸化鉛
の沸点(1470℃)以下では鉛の残留率を20wt%以下に低
減するのが難しくなる。
The lead contained in the waste can be converted into lead chloride and volatilized by firing in the presence of chlorine. However, when an alkali metal coexists, there is a problem in that volatilization due to chlorination of lead is suppressed and lead cannot be separated sufficiently. Comparing the vapor pressures of alkali metal chloride and lead chloride, the vapor pressure of lead chloride is low, so it has been generally thought that the presence of alkali metal does not affect the volatilization of lead. Since lead is more likely to be chloride than lead, when lead and an alkali metal coexist, part of the lead chloride is converted to lead oxide by the alkali metal, and volatilization of lead is suppressed. Therefore, it is difficult to reduce the residual ratio of lead to 20 wt% or less when the boiling point of lead oxide (1470 ° C.) or lower.

【0004】本発明は、廃棄物等から鉛を分離する方法
において、従来の上記問題を解決したものであり、生活
・産業廃棄物等に含まれる鉛の残留率を20wt%以下、
好ましくは10wt%以下に分離してセメント原料として
利用できるようにする鉛の分離方法を提供することを目
的とする。
The present invention solves the above-mentioned conventional problems in a method of separating lead from wastes and the like, and has a lead content of 20% by weight or less contained in household and industrial wastes.
It is an object of the present invention to provide a method for separating lead, which is preferably separated to 10% by weight or less and used as a cement raw material.

【0005】[0005]

【課題を解決するための手段】すなわち、本発明は、鉛
化合物を含有する被処理物を、塩素の存在下で、塩化鉛
の沸点以上に焼成し、鉛化合物を塩化鉛に転じて揮発分
離する方法において、鉛化合物含有量とアルカリ金属化
合物含有量の合計量に見合う量の塩素存在下で焼成する
ことを特徴とする鉛の分離方法に関するものである。
That is, the present invention relates to an object of the present invention is to calcine an object to be treated containing a lead compound in the presence of chlorine to a temperature higher than the boiling point of lead chloride, convert the lead compound into lead chloride and volatilize. The present invention relates to a method for separating lead, characterized by firing in the presence of chlorine in an amount corresponding to the total amount of the lead compound content and the alkali metal compound content.

【0006】本発明の鉛の分離方法は、好ましくは、塩
素の化学当量からアルカリ金属の化学当量を差し引いた
量の鉛の化学当量に対する比(塩素当量比)が−10以
上となる範囲に塩素量を制御し、950〜1500℃の
温度で焼成することにより、鉛を揮発分離する方法を含
む。
In the lead separation method of the present invention, the ratio of chlorine to the chemical equivalent of lead obtained by subtracting the chemical equivalent of alkali metal from the chemical equivalent of chlorine (chlorine equivalent ratio) is preferably -10 or more. The method includes a method of volatilizing and separating lead by controlling the amount and firing at a temperature of 950 to 1500 ° C.

【0007】より具体的には、本発明の鉛分離方法は、
塩素当量比−10〜−5の範囲において1400〜15
00℃の温度で焼成し、塩素当量比−5以上の範囲にお
いて950℃以上の温度で焼成することにより鉛残留率
を20wt%以下に低減する方法を含み、さらに好ましく
は、塩素当量比8以上の範囲で950℃以上の温度で焼
成することにより鉛残留率を3wt%以下に低減する方法
を含む。
More specifically, the lead separation method of the present invention comprises:
In the range of chlorine equivalent ratio -10 to -5, 1400 to 15
The method includes firing at a temperature of 00 ° C. and firing at a temperature of 950 ° C. or more in a range of chlorine equivalent ratio of −5 or more to reduce the lead residual ratio to 20 wt% or less, and more preferably a chlorine equivalent ratio of 8 or more. And reducing the residual ratio of lead to 3 wt% or less by firing at a temperature of 950.degree.

【0008】また、本発明の鉛分離方法は、塩素量は塩
化物の添加量および被処理物の塩化物含有量の合計量で
ある態様を含み、また、被処理物がセメント原料、セメ
ント原料用材料またはコンクリート用材料として利用さ
れるもの、および被処理物の全部または一部が生活・産
業廃棄物である態様を含む。
Further, the lead separation method of the present invention includes an embodiment in which the chlorine amount is the total amount of chloride added and the chloride content of the material to be treated, and the material to be treated is a cement raw material, a cement raw material. The present invention includes an embodiment in which all or a part of the object to be treated is domestic / industrial waste.

【0009】[0009]

【発明の実施の態様】以下、本発明を実施態様に即して
具体的に説明する。本発明の鉛分離方法は、鉛化合物を
含有する被処理物を、塩素の存在下で、塩化鉛の沸点以
上に焼成し、鉛化合物を塩化鉛に転じて揮発分離する方
法において、鉛化合物含有量とアルカリ金属化合物含有
量の合計量に見合う量の塩素存在下で焼成することを特
徴とする。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be specifically described below with reference to embodiments. The lead separation method of the present invention is a method for subjecting an object to be treated containing a lead compound to baking in the presence of chlorine to a temperature equal to or higher than the boiling point of lead chloride, converting the lead compound to lead chloride, and volatilizing and separating the lead compound. It is characterized by firing in the presence of chlorine in an amount corresponding to the total amount of the alkali metal compound and the alkali metal compound content.

【0010】本発明において、被処理物の全部または一
部は都市ゴミ焼却灰、下水汚泥焼却灰、これらの溶融ス
ラグないしその飛灰等の生活廃棄物あるいはシュレッダ
ーダストなどの産業廃棄物などである。これらの焼却灰
等には鉛化合物が通常0.1〜0.5wt%、多いものでは
1.5wt%程度含まれている。また、通常、鉛と共にア
ルカリ金属化合物が1〜10wt%含まれている。なお、
一般に鉛化合物やアルカリ金属化合物と共に銅や亜鉛が
数wt%含まれている。
In the present invention, all or a part of the object to be treated is incinerated ash from municipal waste, incinerated ash from sewage sludge, domestic waste such as molten slag or fly ash thereof, or industrial waste such as shredder dust. . These incinerated ash and the like usually contain a lead compound in an amount of 0.1 to 0.5 wt%, and in most cases, about 1.5 wt%. Further, usually, 1 to 10% by weight of an alkali metal compound is contained together with lead. In addition,
In general, copper and zinc are contained at several wt% together with a lead compound and an alkali metal compound.

【0011】本発明の方法は、上記被処理物を、鉛化合
物含有量とアルカリ金属化合物含有量の合計量に見合う
量の塩素存在下で焼成する。鉛化合物とアルカリ金属化
合物とを共に含むものを塩素存在下で焼成すると、鉛化
合物が塩化鉛に転じて揮発する。この塩化鉛の生成によ
り、図1に示すように、塩化鉛(PbCl2)の沸点(約950℃)
付近で塩素の反応量がピークに達するが、アルカリ金属
塩化物の融点(約800℃)以上では、鉛よりもアルカリ金
属の方が塩化物を生成する傾向が強いため、アルカリ金
属化合物が塩化鉛から塩素を奪って塩化物となり、塩化
鉛の一部は酸化鉛に転じる。この酸化鉛(PbO)の蒸気圧
は塩化鉛の蒸気圧より低いので鉛の揮発が抑制され、鉛
による塩素の反応量は次第に低下する。一方、焼成温度
の上昇に伴い、アルカリ金属塩化物の生成によって塩素
の消費量が増加し、その沸点付近でアルカリ金属による
塩素消費量がピークに達する。従って、アルカリ金属含
有量を除外した鉛化合物の含有量に見合う塩素量では十
分に鉛を揮発分離することができない。
In the method of the present invention, the object to be treated is fired in the presence of chlorine in an amount corresponding to the total amount of the lead compound and the alkali metal compound. When a material containing both a lead compound and an alkali metal compound is fired in the presence of chlorine, the lead compound turns into lead chloride and volatilizes. Due to the formation of lead chloride, as shown in FIG. 1, the boiling point of lead chloride (PbCl 2 ) (about 950 ° C.)
The reaction amount of chlorine reaches a peak in the vicinity, but above the melting point of alkali metal chloride (about 800 ° C), alkali metal has a greater tendency to generate chloride than lead, so that the alkali metal compound becomes lead chloride. From chlorine to chloride, and part of lead chloride turns into lead oxide. Since the vapor pressure of this lead oxide (PbO) is lower than the vapor pressure of lead chloride, the volatilization of lead is suppressed, and the reaction amount of chlorine by lead gradually decreases. On the other hand, as the firing temperature increases, the consumption of chlorine increases due to the generation of alkali metal chloride, and the chlorine consumption by the alkali metal reaches a peak near its boiling point. Therefore, lead cannot be sufficiently volatilized and separated with a chlorine amount corresponding to the content of the lead compound excluding the alkali metal content.

【0012】このように、鉛化合物とアルカリ金属化合
物とを共に含むものを塩素の存在下で焼成することによ
って鉛を揮発分離するには、鉛化合物が塩化鉛に転じる
のに消費される塩素量(ie.鉛化合物含有量に対する塩
素量)と、アルカリ金属化合物によって消費される塩素
量(ie.アルカリ金属化合物に対する塩素量)との合計
量に見合う量の塩素が必要である。
As described above, in order to volatilize and separate lead by calcining a compound containing both a lead compound and an alkali metal compound in the presence of chlorine, the amount of chlorine consumed when the lead compound is converted into lead chloride is determined. An amount of chlorine is necessary which is equal to the total amount of (ie. The amount of chlorine relative to the content of the lead compound) and the amount of chlorine consumed by the alkali metal compound (ie. The amount of chlorine relative to the alkali metal compound).

【0013】具体的な例として、A=(Cl−R)/Pb(Cl
は塩素の化学当量、Rはアルカリ金属の化学当量、Pbは
鉛の化学当量)の式に示すように、鉛の当量に対し、塩
素の当量からアルカリ金属の当量を差し引いた量の比A
(塩素当量比と略称する)を所定範囲に制御する。
As a specific example, A = (Cl-R) / Pb (Cl
Is the chemical equivalent of chlorine, R is the chemical equivalent of the alkali metal, and Pb is the chemical equivalent of lead.) As shown in the equation, the ratio A of the equivalent of lead minus the equivalent of the alkali metal is subtracted from the equivalent of chlorine to the equivalent of lead.
(Abbreviated as chlorine equivalent ratio) within a predetermined range.

【0014】上記塩素当量比の範囲および焼成温度によ
って鉛の残留率は大きく異なる。この関係を図2に示
す。図示するように、塩素当量比が−10未満の範囲で
は焼成温度が1400℃以下では鉛の残留率が20wt%
以上となり、鉛残留率を20wt%以下に低減するには1
400℃以上の温度で焼成する必要がある。この塩素当
量比が−10以上の範囲では、塩素当量比の範囲に応じ
て焼成温度を950〜1500℃に制御することによ
り、鉛の残留率を20wt%以下、好ましくは10wt%以
下に低減することができる。
The residual ratio of lead varies greatly depending on the range of the chlorine equivalent ratio and the firing temperature. This relationship is shown in FIG. As shown in the figure, when the chlorine equivalent ratio is less than -10, when the firing temperature is 1400 ° C. or lower, the residual ratio of lead is 20 wt%.
As mentioned above, to reduce the lead residual ratio to 20 wt% or less, 1
It is necessary to fire at a temperature of 400 ° C. or higher. When the chlorine equivalent ratio is in the range of −10 or more, the firing rate is controlled at 950 to 1500 ° C. in accordance with the range of the chlorine equivalent ratio, so that the residual ratio of lead is reduced to 20% by weight or less, preferably 10% by weight or less. be able to.

【0015】具体的には、塩素当量比が−10〜−5の
範囲では1400〜1500℃の焼成温度で鉛残留率は
概ね10〜20%であり、塩素当量比が−5に近づくに
つれて鉛の残留率が次第に低下し、焼成温度がやや低い
1350℃付近の温度でも鉛の残留率は10〜20%程
度に低減する。塩素当量比が大きくなるにつれて鉛の残
留率が低下する傾向は、塩素当量比が−5以上の範囲に
おいても同様であり、塩素当量比−5〜8に範囲では、
950〜1350℃の焼成温度で鉛残留率が10〜20
wt%に低減し、焼成温度がこれよりやや高く1350〜
1450℃では鉛残留率が更に低減して約10%以下に
なる。また、塩素当量比が8以上の範囲では、950℃
以上の焼成温度、好ましくは1350℃付近の焼成温度
で、鉛残留率を3wt%以下に低減することができる。
Specifically, when the chlorine equivalent ratio is in the range of -10 to -5, the residual ratio of lead is generally 10 to 20% at the firing temperature of 1400 to 1500 ° C., and as the chlorine equivalent ratio approaches -5, the lead content becomes lower. The residual ratio of lead gradually decreases, and the residual ratio of lead is reduced to about 10 to 20% even at a temperature of about 1350 ° C. where the firing temperature is slightly lower. The tendency that the residual ratio of lead decreases as the chlorine equivalent ratio increases is the same even when the chlorine equivalent ratio is in the range of -5 or more, and in the range of the chlorine equivalent ratio of -5 to 8,
The residual ratio of lead is 10 to 20 at a firing temperature of 950 to 1350 ° C.
wt%, firing temperature is slightly higher than 1350 ~
At 1450 ° C., the residual ratio of lead is further reduced to about 10% or less. When the chlorine equivalent ratio is in the range of 8 or more, 950 ° C.
At the above firing temperature, preferably around 1350 ° C., the residual ratio of lead can be reduced to 3 wt% or less.

【0016】上記塩素量は廃棄物が含有する塩化物の量
と、添加する塩化物(塩素源)の量との合計量として定め
ることができる。鉛含有量に対して塩素含有量の多い廃
棄物については、その塩素当量比Aに応じた焼成温度で
加熱する。塩素含有量の少ない廃棄物については塩素源
を添加し、焼成温度との兼ね合いから塩素含有当量Aが
−10以上の適度な範囲になるように塩素源の添加量を
調整して焼成する。塩素源としては塩化カルシウムなど
が適当である。
The amount of chlorine can be determined as the total amount of chloride contained in the waste and the amount of chloride (chlorine source) to be added. The waste having a high chlorine content relative to the lead content is heated at a firing temperature corresponding to the chlorine equivalent ratio A. For waste having a low chlorine content, a chlorine source is added, and the amount of the chlorine source added is adjusted so that the chlorine content equivalent A is in an appropriate range of -10 or more in consideration of the firing temperature, and firing is performed. As a chlorine source, calcium chloride or the like is suitable.

【0017】本発明の方法によって処理された廃棄物は
鉛の含有量が少ないので、セメント原料に適する。従っ
て、都市ゴミ焼却灰や下水汚泥焼却灰あるいはこれらの
溶融スラグや飛灰などを原料として製造されるセメント
の原料として利用することができる。また、セメント原
料用材料あるいはコンクリート用材料として利用するこ
とができる。
The waste treated by the method of the present invention has a low lead content and is suitable as a raw material for cement. Therefore, it can be used as a raw material for cement produced from incinerated municipal ash or sewage sludge ash or their molten slag or fly ash. Further, it can be used as a material for a cement raw material or a material for concrete.

【0018】[0018]

【実施例】以下、本発明を実施例によって具体的に示
す。なお、本発明はこれらの例に限定されない。
EXAMPLES The present invention will be specifically described below with reference to examples. Note that the present invention is not limited to these examples.

【0019】実施例および比較例 表1に示す組成のゴミ焼却灰に、石灰石、塩化カルシウ
ムを加え(焼却灰35wt%、石灰石64wt%、塩化カル
シウム0〜1.5wt%)、これを粉砕・混合して表2に示
す組成の試料を調製した。この試料を表3に示す温度で
焼成し、その鉛残留率を調べた。この結果を表3にまと
めて示した。この結果に示すように塩素当量比および焼
成温度を調整することにより鉛残留率を所望の水準に低
減することができる。
[0019] waste incineration ash having the composition shown in Examples and Comparative Example Table 1, limestone, calcium chloride was added (ash 35 wt%, limestone 64 wt%, calcium chloride 0~1.5wt%), ground and mixed with this Then, a sample having the composition shown in Table 2 was prepared. This sample was fired at the temperature shown in Table 3 and the lead residual ratio was examined. The results are summarized in Table 3. As shown in these results, by adjusting the chlorine equivalent ratio and the firing temperature, the lead residual ratio can be reduced to a desired level.

【0020】[0020]

【表1】 [Table 1]

【0021】[0021]

【表2】 [Table 2]

【0022】[0022]

【表3】 [Table 3]

【図面の簡単な説明】[Brief description of the drawings]

【図1】 鉛とアルカリ金属(Na)の塩素との反応量を
示すグラフ
FIG. 1 is a graph showing the amount of reaction between lead and chlorine of an alkali metal (Na).

【図2】 塩素当量比A〔(Cl−R)/Pb〕と焼成温度に
対する鉛残留率を示すグラフ
FIG. 2 is a graph showing the ratio of lead equivalent to chlorine equivalent ratio A [(Cl-R) / Pb] and firing temperature.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 中野 卓 千葉県佐倉市大作二丁目4番2号 太平洋 セメント株式会社佐倉研究所内 Fターム(参考) 4K001 AA20 BA22 CA13  ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Taku Nakano 2-4-2 Daisaku, Sakura City, Chiba Pref.

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】 鉛化合物を含有する被処理物を、塩素の
存在下で、塩化鉛の沸点以上に焼成し、鉛化合物を塩化
鉛に転じて揮発分離する方法において、鉛化合物含有量
とアルカリ金属化合物含有量の合計量に見合う量の塩素
存在下で焼成することを特徴とする鉛の分離方法。
1. A method for baking an object to be treated containing a lead compound in the presence of chlorine to a temperature equal to or higher than the boiling point of lead chloride, converting the lead compound into lead chloride, and volatilizing and separating the lead compound. A method for separating lead, comprising calcination in the presence of chlorine in an amount commensurate with the total content of metal compounds.
【請求項2】 塩素の化学当量からアルカリ金属の化学
当量を差し引いた量の鉛の化学当量に対する比(塩素当
量比と略称する)が−10以上となる範囲に塩素量を制
御し、950〜1500℃の温度で焼成することにより
鉛を揮発分離する請求項1に記載する鉛の分離方法。
2. The amount of chlorine is controlled within a range where the ratio of the chemical equivalent of lead to the chemical equivalent of lead obtained by subtracting the chemical equivalent of alkali metal from the chemical equivalent of chlorine (abbreviated as chlorine equivalent ratio) is -10 or more. The lead separation method according to claim 1, wherein the lead is volatilized and separated by firing at a temperature of 1500 ° C.
【請求項3】 塩素当量比−10〜−5の範囲において
1400〜1500℃の温度で焼成し、塩素当量比−5
以上の範囲において950℃以上の温度で焼成すること
により鉛残留率を20wt%以下に低減する請求項1また
は2に記載する鉛の分離方法。
3. Firing at a temperature of 1400 to 1500 ° C. in a chlorine equivalent ratio of -10 to -5, and a chlorine equivalent ratio of -5.
3. The method of separating lead according to claim 1, wherein the residual ratio of lead is reduced to 20 wt% or less by firing at a temperature of 950 ° C. or higher in the above range.
【請求項4】 塩素当量比8以上の範囲で950℃以上
の温度で焼成することにより鉛残留率を3wt%以下に低
減する請求項1または2に記載する鉛の分離方法。
4. The method for separating lead according to claim 1, wherein the residual ratio of lead is reduced to 3% by weight or less by baking at a temperature of 950 ° C. or more in a chlorine equivalent ratio of 8 or more.
【請求項5】 塩素量が塩化物の添加量および被処理物
の塩化物含有量の合計量である請求項1〜4のいずれか
に記載する鉛の分離方法。
5. The method for separating lead according to claim 1, wherein the amount of chlorine is a total amount of chloride added and chloride content of the material to be treated.
【請求項6】 被処理物がセメント原料、セメント原料
用材料またはコンクリート用材料である請求項1〜5の
いずれかに記載する鉛の分離方法。
6. The lead separation method according to claim 1, wherein the object to be treated is a cement raw material, a cement raw material, or a concrete material.
【請求項7】 被処理物の全部または一部が生活・産業
廃棄物である請求項1〜6のいずれかに記載する鉛の分
離方法。
7. The method for separating lead according to claim 1, wherein all or a part of the object to be treated is domestic / industrial waste.
JP9345599A 1999-03-31 1999-03-31 Lead separating method Pending JP2000282155A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9345599A JP2000282155A (en) 1999-03-31 1999-03-31 Lead separating method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9345599A JP2000282155A (en) 1999-03-31 1999-03-31 Lead separating method

Publications (1)

Publication Number Publication Date
JP2000282155A true JP2000282155A (en) 2000-10-10

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Family Applications (1)

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Country Status (1)

Country Link
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102586615A (en) * 2012-03-31 2012-07-18 大冶有色金属有限责任公司 Method for efficiently enriching valued metals from complicated sulfur- and lead-containing waste residue
WO2014073399A1 (en) * 2012-11-12 2014-05-15 鳥取県 Method for separating heavy metals from glass

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102586615A (en) * 2012-03-31 2012-07-18 大冶有色金属有限责任公司 Method for efficiently enriching valued metals from complicated sulfur- and lead-containing waste residue
WO2014073399A1 (en) * 2012-11-12 2014-05-15 鳥取県 Method for separating heavy metals from glass
JP2014094366A (en) * 2012-11-12 2014-05-22 Tottori Prefecture Method of separating heavy metal from glass
EP2918352A4 (en) * 2012-11-12 2016-06-22 Tottori Prefecture Method for separating heavy metals from glass

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