JPH10139501A - Slaked lime composition - Google Patents

Slaked lime composition

Info

Publication number
JPH10139501A
JPH10139501A JP8289858A JP28985896A JPH10139501A JP H10139501 A JPH10139501 A JP H10139501A JP 8289858 A JP8289858 A JP 8289858A JP 28985896 A JP28985896 A JP 28985896A JP H10139501 A JPH10139501 A JP H10139501A
Authority
JP
Japan
Prior art keywords
slaked lime
naoh
koh
surface area
specific surface
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
JP8289858A
Other languages
Japanese (ja)
Inventor
Masaru Tamori
勝 田森
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.)
RYOKO SEKKAI KOGYO KK
Original Assignee
RYOKO SEKKAI KOGYO KK
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 RYOKO SEKKAI KOGYO KK filed Critical RYOKO SEKKAI KOGYO KK
Priority to JP8289858A priority Critical patent/JPH10139501A/en
Publication of JPH10139501A publication Critical patent/JPH10139501A/en
Pending legal-status Critical Current

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  • Treating Waste Gases (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Abstract

PROBLEM TO BE SOLVED: To produce a slaked lime composition small in reduction of a specific surface area with the lapse of time and excellent in storage stability by adding a specified amount of an alkali metal hydroxide to the slaked lime. SOLUTION: In this slaked time composition, 0.1-0.7 pts.wt. of an alkali metal hydroxide is incorporated in 100 pts.wt. slaked lime. NaOH and/or KOH is preferable as the alkali metal hydroxide. In the production of the slaked lime composition, a prescribed amount of NaOH and/or KOH are added preferably. For example, NaOH and/or KOH may be added at a grinding stage or may be dissolved previously in water for hydrating calcium oxide. The method is effective for preventing deterioration with the lapse of time of a pulverized slaked lime large in absorption of moisture and CO2 and having >=30m<2> /g specific surface area, and especially effective in the case when the slaked lime composition is stored for 1-2 week in an atmosphere of 30-70% relative humidity.

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】本発明は消石灰組成物に係
り、特に、消石灰の経時的な比表面積の減少を防止し
た、貯蔵安定性に優れた消石灰組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a slaked lime composition, and more particularly to a slaked lime composition excellent in storage stability which prevents the specific surface area of slaked lime from decreasing over time.

【0002】[0002]

【従来の技術】消石灰(水酸化カルシウム)の主要な用
途の一つとして、焼却炉の燃焼排ガスの浄化があるが、
これに用いる消石灰は排ガス中の塩化水素や硫黄酸化物
との反応性の面から、比表面積の大きい微粉であること
が望まれる。
2. Description of the Related Art One of the main uses of slaked lime (calcium hydroxide) is for purification of combustion exhaust gas from incinerators.
Slaked lime used for this purpose is desired to be a fine powder having a large specific surface area from the viewpoint of reactivity with hydrogen chloride and sulfur oxide in exhaust gas.

【0003】しかしながら、消石灰は空気中の水分やC
2 を吸収して次第に比表面積が低下してくる。特に、
比表面積の大きい消石灰は水分やCO2 の吸収速度が高
く、貯蔵中の比表面積の低下量が大きいために、貯蔵環
境によっても異なるが、通常、製造後約2〜3週間で比
表面積は製造時に対して半減してしまう。
[0003] However, slaked lime does not contain moisture in the air or C
The specific surface area gradually decreases by absorbing O 2 . Especially,
Slaked lime with a large specific surface area has a high absorption rate of water and CO 2 and a large decrease in the specific surface area during storage, so it varies depending on the storage environment. It halves over time.

【0004】[0004]

【発明が解決しようとする課題】工場で製造された消石
灰がユーザーにて使用に供されるまで、通常1〜2週間
を要する。このため、比表面積が製造時よりも相当に小
さくなった、従って、反応性がかなり小さくなった消石
灰を使用しているのが現状である。
It usually takes one to two weeks for slaked lime produced in a factory to be used by a user. For this reason, at present, slaked lime whose specific surface area is considerably smaller than that at the time of production, and therefore, reactivity is considerably reduced is used.

【0005】本発明は上記従来の問題点を解決し、経時
的な比表面積の減少量が小さい、貯蔵安定性に優れた消
石灰組成物を提供することを目的とする。
An object of the present invention is to solve the above-mentioned conventional problems and to provide a slaked lime composition having a small amount of decrease in specific surface area with time and excellent storage stability.

【0006】[0006]

【課題を解決するための手段】本発明の消石灰組成物
は、消石灰100重量部に対してNaOH及び/又はK
OH等のアルカリ金属水酸化物0.1〜0.7重量部が
混合されていることを特徴とする。
The slaked lime composition of the present invention comprises NaOH and / or K based on 100 parts by weight of slaked lime.
It is characterized in that 0.1 to 0.7 parts by weight of an alkali metal hydroxide such as OH is mixed.

【0007】消石灰に所定量のNaOH及び/又はKO
Hを混合することにより、消石灰の水分及びCO2 吸収
が防止され、経時的な比表面積の減少量を小さくするこ
とができる。
A predetermined amount of NaOH and / or KO is added to slaked lime.
By mixing H, the absorption of moisture and CO 2 in slaked lime can be prevented, and the decrease in the specific surface area over time can be reduced.

【0008】[0008]

【発明の実施の形態】以下に本発明の実施の形態を詳細
に説明する。
Embodiments of the present invention will be described below in detail.

【0009】本発明の消石灰組成物は、消石灰100重
量部に対して、NaOH及び/又はKOH等のアルカリ
金属水酸化物を0.1〜0.7重量部混合したものであ
る。NaOH及び/又はKOHの割合が消石灰100重
量部に対して0.1重量部未満であると、NaOH及び
/又はKOHを混合したことによる本発明の効果が十分
に得られない。NaOH及び/又はKOHの割合が、消
石灰100重量部に対して0.7重量部を超えると、経
時による比表面積の減少割合は小さいものの、過剰のN
aOH及び/又はKOHが消石灰の微細な消石灰粒子が
構成する凝集粒子の間隙に入り込んでこれをふさぐこと
で、消石灰の初期比表面積自体が小さいものとなり、好
ましくない。また、特にNaOHが多い場合には、Na
OHが混合、粉砕工程で機器内での付着を起こし易く、
その上、NaOHとCO2 との反応で生成したNa2
3 が水分を吸収するようになり、比表面積減少を加速
する場合がある。
The slaked lime composition of the present invention is obtained by mixing 0.1 to 0.7 parts by weight of an alkali metal hydroxide such as NaOH and / or KOH with 100 parts by weight of slaked lime. If the ratio of NaOH and / or KOH is less than 0.1 part by weight with respect to 100 parts by weight of slaked lime, the effect of the present invention caused by mixing NaOH and / or KOH cannot be sufficiently obtained. If the ratio of NaOH and / or KOH exceeds 0.7 parts by weight with respect to 100 parts by weight of slaked lime, the rate of decrease in specific surface area over time is small, but excessive N
If the aOH and / or KOH enter the gaps between the aggregated particles formed by the fine slaked lime particles of slaked lime and close them, the initial specific surface area of the slaked lime itself becomes small, which is not preferable. Further, particularly when NaOH is large, Na
OH easily causes adhesion inside the equipment during the mixing and grinding processes,
In addition, Na 2 C produced by the reaction of NaOH and CO 2
O 3 absorbs water, which may accelerate the specific surface area reduction.

【0010】特に好ましいNaOH及び/又はKOHの
割合は消石灰100重量部に対して0.1〜0.5重量
部である。
A particularly preferred ratio of NaOH and / or KOH is 0.1 to 0.5 part by weight per 100 parts by weight of slaked lime.

【0011】このような本発明の消石灰組成物は、製造
された消石灰に対して所定量のNaOH及び/又はKO
Hを添加混合して製造することも可能であるが、好まし
くは、消石灰の製造工程で所定量のNaOH及び/又は
KOHを添加して製造される。この場合、NaOH及び
/又はKOHの添加工程には特に制限はなく、後述の実
施例に示す如く、消石灰の粉砕工程にNaOH及び/又
はKOHを添加しても良く、また、生石灰水和用の水に
予めNaOH及び/又はKOHを溶解させておいても良
い。
[0011] Such a slaked lime composition of the present invention is prepared by adding a predetermined amount of NaOH and / or KO to the slaked lime produced.
Although H can be added and mixed for production, preferably, it is produced by adding a predetermined amount of NaOH and / or KOH in the slaked lime production process. In this case, the step of adding NaOH and / or KOH is not particularly limited, and NaOH and / or KOH may be added to the step of pulverizing slaked lime, as shown in Examples described later. NaOH and / or KOH may be previously dissolved in water.

【0012】本発明の消石灰組成物は、水分及びCO2
の吸収量が多く、比表面積の減少速度が大きい比表面積
30m2 /g以上の微粉消石灰の経時による劣化防止に
有効であり、特に、このような消石灰組成物を相対湿度
30〜70%の雰囲気で1〜2週間程度貯蔵する場合の
劣化防止に有効である。
The slaked lime composition of the present invention contains water and CO 2
It is effective in preventing the deterioration of fine powder slaked lime having a specific surface area of 30 m 2 / g or more with the lapse of time, which is particularly effective in reducing the specific surface area at a relative humidity of 30 to 70%. Is effective for preventing deterioration when stored for about 1 to 2 weeks.

【0013】なお、本発明の消石灰組成物は、活性炭、
粘土鉱物、その他の添加物を含有するものであっても良
く、例えば、消石灰100重量部に対して活性炭5〜2
0重量部含むダイオキシン吸着能を有する消石灰組成物
にも有効である。
[0013] The slaked lime composition of the present invention comprises activated carbon,
It may contain clay minerals and other additives. For example, activated carbon 5 to 2 with respect to 100 parts by weight of slaked lime
It is also effective for a slaked lime composition having a dioxin adsorption ability containing 0 parts by weight.

【0014】[0014]

【実施例】以下に実施例及び比較例を挙げて本発明をよ
り具体的に説明する。
The present invention will be described more specifically below with reference to examples and comparative examples.

【0015】実施例1〜4,比較例1〜3 消石灰製造能力15kg/時のテストプラントの粉砕工
程にフレーク状のNaOHを所定量添加し、混合と粉砕
を同時に行って、消石灰100重量部に対して表1に示
す量のNaOHが混合された消石灰組成物を製造した
(ただし、比較例1ではNaOH添加せず)。
Examples 1 to 4 and Comparative Examples 1 to 3 A predetermined amount of flake-like NaOH was added to a pulverizing step of a test plant having a slaked lime production capacity of 15 kg / hour, and mixing and pulverizing were simultaneously performed to reduce the amount to 100 parts by weight of slaked lime On the other hand, a slaked lime composition mixed with the amount of NaOH shown in Table 1 was produced (however, in Comparative Example 1, NaOH was not added).

【0016】得られた消石灰組成物を横18cm、縦2
3cmのバットに1cmの厚さに入れ試験試料とした。
この試験試料を相対湿度35%及び65%の一定湿度の
室内にそれぞれ上部解放で放置した。製造直後(0日)
及び放置3日後、7日後、14日後、28日後の消石灰
組成物の比表面積をユアサアイオニクス製モノソープ比
表面積測定器を使用して測定し、結果を表1に示した。
The obtained slaked lime composition is 18 cm wide and 2 cm long.
A test sample was placed in a 3 cm bat at a thickness of 1 cm.
The test sample was left open in a room with a constant humidity of 35% and 65% relative humidity, respectively, with the top open. Immediately after production (0 days)
The specific surface area of the slaked lime composition after 3 days, 7 days, 14 days and 28 days after standing was measured using a monosoap specific surface area measuring device manufactured by Yuasa Ionics, and the results are shown in Table 1.

【0017】[0017]

【表1】 [Table 1]

【0018】実施例5〜8,比較例4,5 実施例1において、NaOHの代りにKOHを用い、消
石灰100重量部に対して表2に示す量のKOHが混合
された消石灰組成物を製造した。
Examples 5 to 8, Comparative Examples 4 and 5 In Example 1, KOH was used in place of NaOH, and a slaked lime composition was prepared by mixing KOH in an amount shown in Table 2 with 100 parts by weight of slaked lime. did.

【0019】この消石灰組成物について実施例1と同様
にして比表面積の経時変化を調べ、結果を表2に示し
た。
With respect to this slaked lime composition, the change with time of the specific surface area was examined in the same manner as in Example 1, and the results are shown in Table 2.

【0020】なお、表2には、比較例1の結果も併記し
た。
Table 2 also shows the results of Comparative Example 1.

【0021】[0021]

【表2】 [Table 2]

【0022】実施例9〜11 実施例1において、NaOHの代りにNaOHとKOH
とを用い、消石灰100重量部に対して表3に示す量の
NaOH及びKOHが混合された消石灰組成物を製造し
た。
Examples 9 to 11 In Example 1, NaOH and KOH were used instead of NaOH.
Was used to produce a slaked lime composition in which NaOH and KOH were mixed in the amounts shown in Table 3 with respect to 100 parts by weight of slaked lime.

【0023】この消石灰組成物について実施例1と同様
にして比表面積の経時変化を調べ、結果を表3に示し
た。
With respect to this slaked lime composition, the change with time in the specific surface area was examined in the same manner as in Example 1, and the results are shown in Table 3.

【0024】[0024]

【表3】 [Table 3]

【0025】前述の如く、工場で製造された消石灰が使
用に供されるまでの期間は1〜2週間であることから、
消石灰は、この1〜2週間以内の期間において比表面積
の減少量が小さいことが望まれる。
As described above, since the time required for slaked lime produced at the factory to be used is 1-2 weeks,
Slaked lime is desired to have a small decrease in the specific surface area in the period of one to two weeks or less.

【0026】表1〜3の通り、NaOH及びKOHを含
まない比較例1では、比表面積の減少量が大きく、特に
相対湿度65%の場合には2週間で半分以下になってい
る。
As shown in Tables 1 to 3, in Comparative Example 1 containing neither NaOH nor KOH, the amount of decrease in the specific surface area was large, and in particular, when the relative humidity was 65%, it was less than half in two weeks.

【0027】これに対して、NaOH及び/又はKOH
を消石灰100重量部に対して0.1〜0.7重量部混
合した実施例1〜11では、比表面積の減少量が小さ
く、特に1〜2週間後の比表面積の減少量が著しく改善
されている。
On the other hand, NaOH and / or KOH
In Examples 1 to 11 in which 0.1 to 0.7 parts by weight was mixed with 100 parts by weight of slaked lime, the decrease in the specific surface area was small, and in particular, the decrease in the specific surface area after 1 to 2 weeks was significantly improved. ing.

【0028】なお、NaOH又はKOHの混合量が少な
い比較例2,4ではNaOH,KOHの添加効果が十分
でなく比表面積の減少量が大きい。
In Comparative Examples 2 and 4 in which the amount of NaOH or KOH was small, the effect of adding NaOH and KOH was not sufficient, and the amount of decrease in the specific surface area was large.

【0029】また、NaOH又はKOHの混合量が多い
比較例3,5では、比表面積の経時減少量は小さいが製
造直後の比表面積が小さい。
In Comparative Examples 3 and 5 in which the amount of NaOH or KOH is large, the specific surface area decreases with time, but the specific surface area immediately after production is small.

【0030】[0030]

【発明の効果】以上詳述した通り、本発明の消石灰組成
物は、比表面積の経時的な減少が小さく、長期貯蔵後に
おいても、高い反応性を維持するものである。
As described in detail above, the slaked lime composition of the present invention has a small decrease in specific surface area with time and maintains high reactivity even after long-term storage.

【0031】従って、本発明の消石灰組成物によれば、
その高い反応性により排ガス処理等における使用量の低
減を図ることができる。
Therefore, according to the slaked lime composition of the present invention,
Due to the high reactivity, it is possible to reduce the amount used in exhaust gas treatment and the like.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 消石灰100重量部に対してアルカリ金
属水酸化物0.1〜0.7重量部が混合されていること
を特徴とする消石灰組成物。
1. A slaked lime composition comprising 100 parts by weight of slaked lime and 0.1 to 0.7 parts by weight of an alkali metal hydroxide.
【請求項2】 請求項1において、アルカリ金属水酸化
物がNaOH及び/又はKOHであることを特徴とする
消石灰組成物。
2. The slaked lime composition according to claim 1, wherein the alkali metal hydroxide is NaOH and / or KOH.
JP8289858A 1996-10-31 1996-10-31 Slaked lime composition Pending JPH10139501A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8289858A JPH10139501A (en) 1996-10-31 1996-10-31 Slaked lime composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8289858A JPH10139501A (en) 1996-10-31 1996-10-31 Slaked lime composition

Publications (1)

Publication Number Publication Date
JPH10139501A true JPH10139501A (en) 1998-05-26

Family

ID=17748679

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8289858A Pending JPH10139501A (en) 1996-10-31 1996-10-31 Slaked lime composition

Country Status (1)

Country Link
JP (1) JPH10139501A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030089192A (en) * 2002-05-17 2003-11-21 (주) 제일금속열처리 Low-noise circular saw
JP2008546631A (en) * 2005-06-28 2008-12-25 ソシエテ アノニム ロワ ルシェルシュ エ ディベロプマン Powdered lime composition, production process thereof and use thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030089192A (en) * 2002-05-17 2003-11-21 (주) 제일금속열처리 Low-noise circular saw
JP2008546631A (en) * 2005-06-28 2008-12-25 ソシエテ アノニム ロワ ルシェルシュ エ ディベロプマン Powdered lime composition, production process thereof and use thereof
US7744678B2 (en) 2005-06-28 2010-06-29 S.A. Lhoist Recherche Et Developpement Powdered lime composition, method of preparing same and use thereof
TWI395713B (en) * 2005-06-28 2013-05-11 Lhoist Rech & Dev Sa Powdered lime composition, method of preparing same and use thereof

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