JP2709554B2 - Ladle electrode heating and refining method for molten steel - Google Patents

Ladle electrode heating and refining method for molten steel

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Publication number
JP2709554B2
JP2709554B2 JP30273092A JP30273092A JP2709554B2 JP 2709554 B2 JP2709554 B2 JP 2709554B2 JP 30273092 A JP30273092 A JP 30273092A JP 30273092 A JP30273092 A JP 30273092A JP 2709554 B2 JP2709554 B2 JP 2709554B2
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JP
Japan
Prior art keywords
slag
steel
molten steel
basicity
refining
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.)
Expired - Fee Related
Application number
JP30273092A
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Japanese (ja)
Other versions
JPH06145764A (en
Inventor
雅之 荒井
文夫 小泉
安夫 山上
一 磯田
健治 立野
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.)
Nippon Steel Corp
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Nippon Steel Corp
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Filing date
Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP30273092A priority Critical patent/JP2709554B2/en
Publication of JPH06145764A publication Critical patent/JPH06145764A/en
Application granted granted Critical
Publication of JP2709554B2 publication Critical patent/JP2709554B2/en
Anticipated expiration legal-status Critical
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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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  • Treatment Of Steel In Its Molten State (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】本発明は溶鋼の二次精錬工程であ
る取鍋電極加熱精錬(以下LFと言う)法に関するもの
である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a ladle electrode heating and refining (hereinafter referred to as LF) method as a secondary refining process for molten steel.

【0002】[0002]

【従来の技術】近年、鋼材に対する品質要求はその利用
技術の高度化、多様化とともに厳しさを増し、高純度鋼
製造へのニーズは益々高まっている。このような高純度
鋼製造の要求に対して製鋼工程では溶銑予備処理あるい
は二次精錬設備の拡充をはかってきた。特に溶鋼の脱S
及び脱介在物をはかる精錬については、強還元且つ高塩
基度スラグによる精錬が必要であり、LFプロセスの導
入によりこのスラグ精錬が可能となり、低S鋼及び高清
浄度鋼の製造工程能力が大幅に向上した。
2. Description of the Related Art In recent years, the quality requirements for steel materials have become increasingly severe with the sophistication and diversification of their utilization techniques, and the need for high-purity steel production has been increasing. In response to such demands for the production of high-purity steel, the steelmaking process has attempted to expand the hot metal pretreatment or secondary refining equipment. In particular, removal of molten steel S
For refining to measure inclusions and de-inclusions, refining with strong reduction and high basicity slag is necessary, and the introduction of the LF process makes this slag refining possible, significantly increasing the production process capacity of low S steel and high cleanliness steel. Improved.

【0003】従来の技術として、LF工程においてはス
ラグ塩基度の高位確保及び徹底したスラグ酸化度(Fe
O+MnO)の低減をはかることにより、脱S反応促進
あるいは鋼中介在物の低減をはかることが一般的に行わ
れている(例えば、日本鉄鋼協会:第126・127回
西山記念技術講座、1988)。また一方では近年にお
いて、高清浄度を要求される鋼種の中においても鋼材の
被削性を向上させるために積極的にSを添加し、鋼中S
濃度を高くする必要がある鋼種が増加傾向にある。しか
し、上記のとおり従来のLF工程でのスラグ精錬技術で
は、溶鋼の清浄化と脱Sが同時に促進されてしまい、現
状の清浄度を確保するための高塩基度操業では、添加し
たSの溶鋼中への溶解割合が低く、多量にSを添加する
必要があった。
As a conventional technique, in the LF process, a high slag basicity is secured and a thorough slag oxidation degree (Fe
It is generally practiced to reduce the amount of O + MnO) to promote the de-S reaction or reduce inclusions in the steel (for example, Japan Iron and Steel Institute: 126th and 127th Nishiyama Memorial Technical Course, 1988). . On the other hand, in recent years, even in steel types that require high cleanliness, S is actively added to improve the machinability of steel materials,
There is an increasing trend for steel types that require higher concentrations. However, as described above, in the conventional slag refining technology in the LF process, the purification of molten steel and the removal of S are simultaneously promoted, and in the high basicity operation for securing the current cleanliness, the molten steel of added S The rate of dissolution in the medium was low, and a large amount of S had to be added.

【0004】[0004]

【発明が解決しようとする課題】このように高清浄且つ
被削性を有する鋼種の従来LF精錬においては、脱介在
物を目的とする高清浄化処理を優先するためスラグ塩基
度を高くせざるを得ず、Sの添加歩留が低下することに
より多量にSを添加する必要がある。また、LF処理を
行うに当たっては生石灰、アルミナ、軽焼ドロマイト等
の高価な造滓材を添加し、さらに滓化させるため、精錬
前溶鋼の十分な熱裕度の確保が必要であることなどの改
善すべき課題がある。
In the conventional LF refining of a steel type having high cleanliness and machinability as described above, it is necessary to increase the basicity of slag in order to give priority to the high purification treatment for removing inclusions. However, it is necessary to add a large amount of S due to a decrease in the yield of S addition. In addition, in performing the LF treatment, it is necessary to add a high-grade slag forming material such as quicklime, alumina, and lightly-burned dolomite, and to further form a slag. There are issues to be improved.

【0005】本発明は前記従来法の問題点を解決できる
LF操業法の提供を目的とする。
An object of the present invention is to provide an LF operation method capable of solving the problems of the conventional method.

【0006】[0006]

【課題を解決するための手段】すなわち本発明は、溶鋼
の二次精錬工程の一つであるLF処理において、高塩基
度且つ低酸化度スラグにより脱Sを行った後、該高S含
有スラグを回収し、これを高S鋼で脱Sを抑制すること
が必要な鋼種の精錬に再使用するに際して、珪石等のS
iO 2 源を添加することによりスラグ塩基度を3〜5に
制御して精錬することを特徴とするLF精錬法を要旨と
する。
That is, in the present invention, in the LF treatment which is one of the secondary refining processes of molten steel, after removing S by a high basicity and a low oxidation degree slag, the high S content slag is obtained. Is recovered and reused in the refining of steel types that require high S steel to suppress the removal of S.
Add slag basicity to 3-5 by adding iO 2 source
Control to the gist of LF refining method characterized by refining.

【0007】[0007]

【0008】[0008]

【作用】従来、LF処理は図1の従来法に示す工程で行
っており、毎回新規の造滓材を添加していた。本発明者
らは、図1の本発明法に示すように、LFにて脱S処理
を行った後の高塩基度(CaO/SiO2 )、低酸化度
(T.Fe+MnO)であり、且つ高S含有のスラグを
LFでの脱S抑制が必要な処理に再使用すると、S添加
歩留が向上し、溶鋼中の介在物を生成する鋼中T[O]
の増大を伴なわずに、さらに従来処理法に比較してスラ
グの生成が迅速となり、LFトータルの処理時間が短縮
され、大幅なエネルギーコストの削減が可能であること
を見出した。
Conventionally, the LF treatment has been carried out in the step shown in the conventional method of FIG. 1, and a new slag material has been added each time. The present inventors, as shown in the method of the present invention in FIG. 1, have a high basicity (CaO / SiO 2 ), a low oxidation degree (T.Fe + MnO) after de-S treatment by LF, and When the slag containing high S is reused in the processing that requires the suppression of the removal of S by LF, the yield of S addition is improved, and T [O] in the steel that generates inclusions in the molten steel is improved.
It has been found that the slag is generated more quickly than the conventional processing method, the LF total processing time is shortened, and the energy cost can be significantly reduced without increasing the conventional method.

【0009】即ちLF工程での脱S反応は次の式にて説
明される。 〔S〕+(O2+) = (S2+)+〔O〕………………(1) 〔S〕+(CaO)=(CaS)+〔O〕………………(2) 従って、溶鋼の脱S反応を抑制するためには、(1)式
右辺のスラグ中(S2+)または溶鋼中〔O〕の活量を増
大させるか、あるいは(1)式左辺のスラグ中(O2+
の活量を低下させることが有効である。この内、〔O〕
活量の増大及び(O2+)活量の低下はスラグ酸化度が上
昇し、且つ(2)式のスラグ中(CaO)が低下するこ
とによる塩基度の低下を伴うことから、溶鋼の高清浄度
を維持しつつ脱S反応を抑制するためには、スラグ中の
(S2+)の活量増大が最も有効であることは物理化学的
に明らかである。
That is, the S removal reaction in the LF step is described by the following equation. (S) + (O 2+ ) = (S 2+ ) + [O] (1) [S] + (CaO) = (CaS) + [O] (...) ( 2) Therefore, in order to suppress the de-S reaction of molten steel, the activity of (S 2+ ) in the right side of equation (1) or the activity of [O] in molten steel must be increased, or the left side of equation (1) In slag (O 2+ )
It is effective to decrease the activity. Of these, [O]
An increase in the activity and a decrease in the (O 2+ ) activity are accompanied by an increase in the slag oxidation degree and a decrease in the basicity due to a decrease in (CaO) in the slag in the formula (2). It is physicochemically clear that increasing the activity of (S 2+ ) in the slag is most effective in suppressing the de-S reaction while maintaining the cleanliness.

【0010】よって脱S後のS含有量の高いスラグの再
使用によりスラグの高塩基度、低酸化度を維持しつつ、
スラグ中のSの活量を高めることが可能となり、溶鋼の
清浄度を低下させずに脱S反応を抑制できることにな
る。本発明者らは、上記目標とする反応を実機で確認し
たところ、図2に示すとおり生石灰、アルミナ、軽焼ド
ロマイト等の新規造滓材をそれぞれ添加して処理する従
来法より、脱S後のS含有率が0.25〜0.35%と
高い高塩基度、低酸化度のスラグを再使用する本発明法
の方が溶鋼の脱S率が低下するのが確認された。さら
に、図2に示すとおり、LF処理後スラグ塩基度5近傍
より溶鋼の脱S率は急減し、また図3に示すとおりスラ
グ塩基度が3近傍よりスラグ酸化度の指標であるスラグ
中のT.Fe濃度が急増することを見出した。従ってL
F脱S後のスラグを再使用することでスラグ中のS濃度
を高め、Sの活量を高位に保持し、且つ上記範囲にスラ
グ中の塩基度を制御することによって、脱S反応をさら
に効率的に抑制でき、より高S含有の高清浄度鋼製造へ
の適用が可能となる。
[0010] Therefore, by reuse of the slag having a high S content after de-S, while maintaining the high basicity and low oxidation degree of the slag,
The activity of S in the slag can be increased, and the S removal reaction can be suppressed without lowering the cleanliness of the molten steel. The present inventors have confirmed the above-mentioned target reaction with an actual machine. As shown in FIG. 2, after the conventional method of adding and treating a new slag forming material such as quicklime, alumina, lightly burned dolomite, and the like, It was confirmed that the method of the present invention in which slag having a high basicity and a low oxidation degree was reused, which had a high S content of 0.25 to 0.35%, had a lower S removal rate of molten steel. Further, as shown in FIG. 2, the desulfurization rate of the molten steel decreases sharply from the vicinity of slag basicity 5 after the LF treatment, and as shown in FIG. . It has been found that the Fe concentration sharply increases. Therefore L
By increasing the S concentration in the slag by reusing the slag after the F de-S, maintaining the activity of S at a high level, and controlling the basicity in the slag to the above range, the de-S reaction is further increased. It can be suppressed efficiently and can be applied to the production of high-purity steel with a higher S content.

【0011】塩基度の制御は、珪石等のSiO2 源を添
加することにより制御可能であり、添加量については再
使用するスラグの組成及び量より容易に決定できる。と
ころで、LF脱S抑制処理後スラグは、再度LF脱S処
理に利用することも可能であり、この場合は、生石灰等
の添加による高塩基度レベルへのスラグ組成コントロー
ルが必要である。
The basicity can be controlled by adding an SiO 2 source such as silica stone, and the amount of addition can be easily determined from the composition and amount of the slag to be reused. By the way, the slag after the LF de-S suppression processing can be used again for the LF de-S processing. In this case, it is necessary to control the slag composition to a high basicity level by adding quicklime or the like.

【0012】また、スラグの再使用法については、安全
を考慮する上で排滓・冷却後、破砕し、フレコンバック
詰めにて添加する方法が最適と考えられるが、この限り
ではない。
Regarding the method of reusing the slag, it is considered that, in consideration of safety, a method of crushing after discharging and cooling, crushing, and adding the slag in a flexible container bag is not limited thereto.

【0013】[0013]

【実施例】脱S及び低酸素化精錬を行ったLF処理後ス
ラグを回収し、LFにおける脱S抑制処理に該回収スラ
グを10kg/T再使用した。表1は脱S及び低酸素化
処理を行った鋼種の成分系と脱S抑制処理を行った鋼種
の成分系を示す。また表2は脱S処理後回収したスラグ
組成及び該スラグを脱S抑制処理に再使用した後のスラ
グ組成及び品質状況を示す。さらに表3に比較のために
従来法にて脱S抑制処理を行った実績も併せて示す。こ
こで従来法とは、生石灰、軽焼ドロマイト、アルミナ等
の造滓材を新たに添加し、処理に必要なスラグを生成さ
せて処理する方法を示す。
EXAMPLE Slag after LF treatment after removal of S and deoxygenation was recovered, and the recovered slag was reused at 10 kg / T for suppression of removal of S in LF. Table 1 shows the component systems of the steel types subjected to the de-S and oxygen reduction treatments and the component systems of the steel types subjected to the de-S suppression treatment. Table 2 shows the slag composition recovered after the de-S treatment and the slag composition and quality status after the slag was reused in the de-S control processing. Further, Table 3 also shows the results of performing the desulfurization suppression processing by the conventional method for comparison. Here, the conventional method refers to a method of newly adding a slag-making material such as quicklime, lightly-burned dolomite, and alumina to generate slag necessary for the treatment.

【0014】表3に示す結果から分かるように、従来法
に比較して本発明法による溶鋼清浄度(T[O]レベ
ル)は従来法並が得られており、問題は見られず、さら
に本発明法では再使用スラグを用いることにより滓化時
間が短縮されるため、LF総処理時間が短縮され、その
他LF添加S歩留が向上し、造滓材である生石灰等の使
用量も低減した。
As can be seen from the results shown in Table 3, compared with the conventional method, the cleanliness of molten steel (T [O] level) according to the method of the present invention is comparable to that of the conventional method, and no problem is observed. In the method of the present invention, the slagification time is shortened by using the reused slag, so that the LF total treatment time is shortened, the LF addition S yield is improved, and the amount of lime used as slag forming material is also reduced. did.

【0015】[0015]

【表1】 [Table 1]

【0016】[0016]

【表2】 [Table 2]

【0017】[0017]

【表3】 [Table 3]

【0018】[0018]

【発明の効果】以上の説明からわかるように本発明によ
れば次のような効果が奏される。第1は、LF処理中の
脱S反応が抑制され、添加するS歩留が向上すること、
さらに下工程であるRHあるいは連鋳工程における鋼中
S濃度の低下が抑制されることである。即ち、鋼中S濃
度を高めて被削性の向上をはかる必要のある鋼種につい
ては、本発明は有効であり、容易に必要な塩基度が制御
できることから清浄度の維持(介在物量の低減)が可能
となる。
As will be understood from the above description, the present invention has the following effects. First, the removal of S during the LF treatment is suppressed, and the yield of added S is improved.
Further, the lowering of the S concentration in the steel in the RH or the continuous casting step, which is a lower step, is suppressed. That is, the present invention is effective for a steel type which needs to improve the machinability by increasing the S concentration in the steel to maintain the cleanness (reduction of the amount of inclusions) since the required basicity can be easily controlled. Becomes possible.

【0019】第2は、LF工程における添加フラックス
量の大幅削減がはかられること、さらに第3としてスラ
グの滓化が迅速であり、LFの処理時間が短縮され、エ
ネルギーあるいは耐火物コストの削減がもたらされるこ
とである。
Second, the amount of added flux in the LF process can be greatly reduced. Third, the slag can be quickly turned into slag, the LF processing time can be shortened, and energy or refractory costs can be reduced. Is brought.

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

【図1】従来法および本発明法の工程を対比して示す図
である。
FIG. 1 is a diagram showing steps of a conventional method and a method of the present invention in comparison.

【図2】LF処理後スラグ塩基度と脱S率の関係を表す
図である。
FIG. 2 is a diagram showing the relationship between the slag basicity after LF treatment and the S removal rate.

【図3】LF処理後スラグ塩基度とスラグ中T.Fe含
有率の関係を表す図である。
FIG. 3 shows slag basicity and TF in slag after LF treatment. It is a figure showing the relationship of Fe content.

フロントページの続き (72)発明者 磯田 一 北海道室蘭市仲町12番地 新日本製鐵株 式会社 室蘭製鐵所内 (72)発明者 立野 健治 北海道室蘭市仲町12番地 新日本製鐵株 式会社 室蘭製鐵所内 (56)参考文献 特開 昭61−174314(JP,A)Continued on the front page (72) Inventor Kazuo Isoda 12 Nakamachi, Muroran City, Hokkaido Nippon Steel Corporation Muroran Works (72) Inventor Kenji Tateno 12 Nakamachi, Muroran City, Hokkaido Nippon Steel Corporation Muroran Inside the ironworks (56) References JP-A-61-174314 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 溶鋼の二次精錬工程である取鍋電極加熱
精錬法において、高塩基度且つ低酸化度スラグによ
S処理を行った後、該スラグ回収し、高S鋼の脱S抑
制精錬に再使用するに際して、スラグ塩基度が下記の範
囲を満足するようにSiO 2 源を添加することを特徴と
する溶鋼の取鍋電極加熱精錬法。3≦スラグ塩基度;(%CaO/%SiO 2 )≦5
1. A ladle electrode heating refining method, which is molten steel secondary refining step, after the de-S process that due to the high basicity and low oxidation degree slag, and recovering the slag, a high S steel Escape from S
When reused in refining, the slag basicity is in the following range.
A ladle electrode heating and refining method for molten steel, characterized by adding a SiO 2 source so as to satisfy the requirements. 3 ≦ slag basicity; (% CaO /% SiO 2 ) ≦ 5
JP30273092A 1992-11-12 1992-11-12 Ladle electrode heating and refining method for molten steel Expired - Fee Related JP2709554B2 (en)

Priority Applications (1)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30273092A JP2709554B2 (en) 1992-11-12 1992-11-12 Ladle electrode heating and refining method for molten steel

Publications (2)

Publication Number Publication Date
JPH06145764A JPH06145764A (en) 1994-05-27
JP2709554B2 true JP2709554B2 (en) 1998-02-04

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