JPH0481488A - Production of gas sealing member - Google Patents

Production of gas sealing member

Info

Publication number
JPH0481488A
JPH0481488A JP2196602A JP19660290A JPH0481488A JP H0481488 A JPH0481488 A JP H0481488A JP 2196602 A JP2196602 A JP 2196602A JP 19660290 A JP19660290 A JP 19660290A JP H0481488 A JPH0481488 A JP H0481488A
Authority
JP
Japan
Prior art keywords
seal member
gas seal
gas
felt
aqueous solution
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
JP2196602A
Other languages
Japanese (ja)
Other versions
JP2858363B2 (en
Inventor
Hironao Numamoto
浩直 沼本
Atsushi Nishino
敦 西野
Jiro Suzuki
次郎 鈴木
Yukiyoshi Ono
之良 小野
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP2196602A priority Critical patent/JP2858363B2/en
Publication of JPH0481488A publication Critical patent/JPH0481488A/en
Application granted granted Critical
Publication of JP2858363B2 publication Critical patent/JP2858363B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Gasket Seals (AREA)
  • Catalysts (AREA)
  • Sealing Material Composition (AREA)
  • Inorganic Fibers (AREA)
  • Nonwoven Fabrics (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はガス 石油の未燃焼混合気を触媒燃焼するガス
シール部材の製造方法に関すム従来の技術 従来のガスシール部材は耐熱性無機繊維をシート状 フ
ェルト状またはブランケット状に加工しこれらを使用し
たい場所に圧縮した状態で挟み込んで使用してい島 し
かし これでは燃焼体とそれを保持する枠体との隙間を
充分にガスシールすることが困難であった そのため燃焼装置の一つである触媒燃焼装置では高濃度
の未燃焼混合気をハニカム形状の燃焼体に供給し燃焼さ
せも そのときに燃焼体とそれを保持する枠体の隙間の
シール部かられずかなガス漏れが生じて耘 未燃焼ガス
は著しい臭気を発生すそこで燃焼体とそれを保持する枠
体との隙間には充分な注意を払う必要があり、従来の無
機繊維シール部材て そのシール性を改善するためには
ガスシール部材のかさ密度を大きくし ち密にしなけれ
ばらなかった 発明が解決しようとする課題 しかし 従来のガスシール部材において、そのかさ密度
を大きくしち密にするとガスシール部材のクツション性
が失われてくa その結果 燃焼状態で高温になった燃焼体と枠体とはと
もに膨張する力丈 熱膨張に差がある場合(一般には枠
体は金入 燃焼体はセラミックであり、枠体の方が燃焼
体よりも熱膨張係数が大きい)にはクツション性の失わ
れたシール部材では隙間ができ、未燃焼ガスがスリップ
し易く、これを従来のガスシール部材で防止しようとす
ることは困難であった 本発明は上記のような従来の課題を解決するもの玄 米
燃焼ガスを触媒燃焼し 適度のクツション性を有するガ
スシール部材の製造方法の提供を目的とすも 課題を解決するための手段 上記の目的を達成するために本発明のガスシール部材の
製造方法ζよ 耐熱性無機繊維からなるシートまたはフ
ェルトに水溶性高分子と希土類金属塩を含む水溶液を含
浸し その後乾燥、 熱分解して希土類金属酸化物をシ
ートまたはフェルト中に分散担持させ、さらにその後白
金族系金属を担持させも 作用 本発明は上記した構成により、無機繊維に希土類金属酸
化物が均一に分散担持され 熱劣化が少なく、適度のク
ツション性を有するガスシール部材が得られも 実施例 以下、本発明の実施例について説明する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a method for manufacturing a gas seal member for catalytically combusting an unburned mixture of gas or oil.Background ArtA conventional gas seal member is made of a sheet of heat-resistant inorganic fibers. It is used by processing it into a felt or blanket shape and compressing it and putting it in the place where you want to use it. However, with this method, it is difficult to sufficiently seal the gap between the combustion body and the frame that holds it. Therefore, in a catalytic combustion device, which is one type of combustion device, a highly concentrated unburned air-fuel mixture is supplied to a honeycomb-shaped combustion body and combusted. Unburned gas generates a strong odor. Therefore, it is necessary to pay sufficient attention to the gap between the combustion body and the frame that holds it, and conventional inorganic fiber seal members In order to improve the sealing performance, the bulk density of the gas seal member must be increased and the gas seal member must be made denser.However, in conventional gas seal members, if the bulk density is increased and the gas seal member is made denser, the gas seal member becomes As a result, the combustion body and the frame expand at a high temperature during combustion.If there is a difference in thermal expansion (generally, the frame is made of gold and the combustion body is made of ceramic). , the frame body has a larger coefficient of thermal expansion than the combustion body), a sealing member that has lost its cushioning properties creates a gap, making it easy for unburned gas to slip.We tried to prevent this with conventional gas sealing members. The present invention solves the above-mentioned conventional problems, and aims to provide a method for manufacturing a gas seal member that catalytically burns brown rice combustion gas and has appropriate cushioning properties. Means for Solving In order to achieve the above object, the method for manufacturing a gas seal member of the present invention is as follows: A sheet or felt made of heat-resistant inorganic fibers is impregnated with an aqueous solution containing a water-soluble polymer and a rare earth metal salt, and then dried. , The rare earth metal oxide can be dispersed and supported on the sheet or felt by thermal decomposition, and then the platinum group metal can be supported thereon.The present invention has the above-described structure, so that the rare earth metal oxide is evenly dispersed and supported on the inorganic fiber. EMBODIMENTS OF THE INVENTION Examples of the present invention will be described below.

実施例1 アルミナ 70wt販 シリカ 30wt翅繊維長繊維
長0m爪 繊維径 約3μmのアルミナシリカの無機繊
維からなる厚み8mmのフェルト(かさ密度 0. 1
8g/cc)に水溶性高分子としてポリエチレングリコ
ール(分子量 約20000)10wt%と希土類金属
塩として0゜1モル硝酸セリウムを含む水溶液を含浸後
、 80℃で1時間転速 500℃で30分間熱処理し
て酸化セリウムをアルミナシリカ繊維に対して18wt
%分散担持させ丸 その後このガスシール部材を塩化白
金酸の水溶液に浸漬し 乾燥 熱処理を行t\ 白金を
0.1wt%担持し九  本実施例で得られたガスシー
ル部材1を第1図のような触媒燃焼装置に使用し シー
ル部での炭化水素の漏れをシール部から1cm離れたと
ころに2mmφのノズルを設は測定することにより評価
し九触媒燃焼装置は空燃比をm=1.70とし 燃焼体
2に6 kcal・h/cm2の燃焼負荷をかけ、燃焼
体2を約800℃に加熱し丸 な抵 第1図において、
3は燃焼体2を保持する枠恢 4は燃料ガス供給a 5
は送風a 6は予混合気室 7は排出部であム また ガスシール部材寿命試験として上記燃焼状態を1
時間続けた後消火し 30分間冷却する工程を1サイク
ルとり、、2000サイクル後に再度上記燃焼状態での
ガスシール性を評価し九比較例1 実施例1のガスシール部材に代えてアルミナシリカ繊維
のみからなる厚み8mmのフェルトを比較例1としな 比較例2 比較例1のガスシール部材を塩化白金酸の水溶液に浸漬
し 転速 熱処理を行〜\ 白金を0. 1wt%担持
したガスシール部材を比較例2とした比較例3 実施例1において、ポリエチレングリコールを添加しな
い硝酸セリウム水溶液を使用して酸化セリウムをアルミ
ナシリカ繊維に対して18wt%分散担持させた その
後、塩化白金酸の水溶液に浸漬し 転速 熱処理を行1
.X、白金を0.1wt%担持したガスシール部材を比
較例3としへ比較例1、比較例2、比較例3で得られた
ガスシール部材のシール性も実施例1と同様な条件で測
定し九 実施例1、比較例1、比較例2、比較例3について初期
と2000サイクル後の結果を表1に示す。
Example 1 Alumina 70wt sales Silica 30wt wing fiber long fiber length 0m nail 8mm thick felt (bulk density 0.1
8 g/cc) was impregnated with an aqueous solution containing 10 wt% of polyethylene glycol (molecular weight approximately 20,000) as a water-soluble polymer and 0.1 mole of cerium nitrate as a rare earth metal salt, then rotated at 80°C for 1 hour and heat treated at 500°C for 30 minutes. and add 18wt of cerium oxide to alumina-silica fiber.
After that, this gas seal member was immersed in an aqueous solution of chloroplatinic acid, dried, and heat-treated.The gas seal member 1 obtained in this example was shown in FIG. When used in a catalytic combustion device such as Then, a combustion load of 6 kcal h/cm2 was applied to the combustion body 2, and the combustion body 2 was heated to about 800°C.
3 is a frame that holds the combustion body 2; 4 is a fuel gas supply a; 5
is the air blower a, 6 is the premixture chamber, 7 is the exhaust part, and the above combustion condition is 1 as a gas seal member life test.
After 1 cycle of extinguishing and cooling for 30 minutes, the gas sealing properties under the above combustion conditions were evaluated again after 2,000 cycles.9 Comparative Example 1 Only alumina-silica fiber was used instead of the gas seal member of Example 1. Comparative Example 1 and Comparative Example 2 The gas seal member of Comparative Example 1 was immersed in an aqueous solution of chloroplatinic acid, and subjected to rotational heat treatment. Comparative Example 3 in which a gas seal member carrying 1 wt% was used as Comparative Example 2 In Example 1, 18 wt% of cerium oxide was dispersed and supported on alumina-silica fiber using a cerium nitrate aqueous solution to which polyethylene glycol was not added. Immersed in an aqueous solution of chloroplatinic acid, rotated and heat treated 1
.. X, a gas seal member carrying 0.1 wt% platinum was used as Comparative Example 3. The sealing performance of the gas seal members obtained in Comparative Example 1, Comparative Example 2, and Comparative Example 3 was also measured under the same conditions as in Example 1. Table 1 shows the results of Example 1, Comparative Example 1, Comparative Example 2, and Comparative Example 3 at the initial stage and after 2000 cycles.

表1 この結果 本実施例によるガスシール部材は優れたガス
シール性を示していム すなわ板 比較例1では最初か
ら充分なガスのシールを行うことができなかった また
 比較例2では初期においては優れたガスシール性を示
した力丈 その後に熱劣化が進収 シール部材に担持さ
れた触媒金属が浄化効果を発揮できなくなった また 
比較例3は本実施例とほぼ同等レベルのガスシール性を
示し丸 しかし 本実施例と比較例3のガスシール部材
に対して厚み8mmの断面方向に酸化セリウムの分散状
態を分析すると、第2図(A)、第2図(B)に示すよ
うに比較例3では酸化セリウムの分布にかなりむらがあ
り、表面側に比べて中心部における担持量が少なくなっ
ているのに対し本実施例ではほぼ均一な担持状態となっ
ていた その結果 ガスシール部材の寿命試験において
本実施例の方が比較例3よりも優れた性能を示したここ
て ガスシール部材中での酸化セリウム分布を均一にす
るため添加するポリエチレングリコールの量は水溶液中
に約2〜15wt%である時有効であっな そして、使
用するポリエチレングリコールの分子量が大きい時(分
子量 約60000)は少量で約2〜ewt%程度、分
子量が小さい時(分子量 約8000)は約10〜15
wt%程度が好まし賎 実施例2 実施例1で使用したのと同じアルミナシリカ繊維フェル
トに水溶性高分子としてポリエチレングリコール(分子
量 約20000)を10wt翅希土類金属塩として硝
酸セリウムを0.02〜0゜4モルを含む水溶液を含浸
[80℃で1時間転速 500℃で30分間熱処理し 
酸化セリウムを分散担持させ丸 その免 そのガスシー
ル部材を塩化白金酸の水溶液に浸饗 転速 熱処理を行
t、X  白金を0.1wt%担持した 得られたガス
シール部材のシール性は実施例1と同様の条件で測定し
九 また ガスシール部材のクツション性(復元性)につい
て41  部材をIcm”に切り出し プレスで10k
g/cm”の荷重をかけた後の復元率で評価し九 ここで復元率(%)=(荷重後の厚み)/(荷重前の厚
み)であム その結果を表2に示す。
Table 1 Results The gas seal member according to this example exhibited excellent gas sealing properties. Strength that showed excellent gas sealing properties After that, thermal deterioration progressed The catalytic metal supported on the sealing member was no longer able to exert its purification effect.
Comparative Example 3 showed almost the same level of gas sealing performance as this Example. As shown in Figures (A) and 2 (B), in Comparative Example 3, the distribution of cerium oxide was quite uneven, and the amount supported in the center was smaller than on the surface side, whereas in this example As a result, in the life test of the gas seal member, this example showed better performance than Comparative Example 3.The cerium oxide distribution in the gas seal member was made uniform. Therefore, it is effective when the amount of polyethylene glycol added to the aqueous solution is about 2 to 15 wt%.And when the molecular weight of the polyethylene glycol used is large (molecular weight of about 60,000), a small amount of about 2 to 15 wt% is added. When the molecular weight is small (molecular weight approximately 8000), it is approximately 10 to 15
About wt% is preferable.Example 2: 10wt of polyethylene glycol (molecular weight: about 20,000) as a water-soluble polymer was added to the same alumina-silica fiber felt as used in Example 1, and cerium nitrate was added as a rare earth metal salt of 0.02~ Impregnated with an aqueous solution containing 0.4 mol [rolled at 80°C for 1 hour, heat treated at 500°C for 30 minutes]
Cerium oxide was dispersed and supported, and the gas seal member was immersed in an aqueous solution of chloroplatinic acid, rotated, and heat treated. Measurements were made under the same conditions as in 1. Regarding the cushioning properties (restorability) of gas seal members: 41 Cut the member into Icm" pieces and press to 10k.
It was evaluated based on the recovery rate after applying a load of "g/cm".Here, recovery rate (%)=(thickness after load)/(thickness before load).The results are shown in Table 2.

実施例3 かさ密度 0. 29g/cc、  厚み8mmのアル
ミナシリカ繊維フェルトに水溶性高分子としてポリエチ
レングリコール(分子量 約20000)10wt% 
 希土類金属塩として硝酸セリウムを0、02〜0.2
0モル含む水溶液を含浸機 80℃で1時間乾燥 50
0℃で30分間熱処理し酸化セリウムを分散担持させた
 その徽 それぞれのガスシール部材を塩化白金酸の水
溶液に浸漬し 転速 熱処理を行(\ 白金を0.1w
t%担持しtも  得られたガスシール部材のシール性
は実施例1と同様な条件で測定し九 それらの結果を表
3に示す。
Example 3 Bulk density 0. 29g/cc, 8mm thick alumina silica fiber felt with 10wt% polyethylene glycol (molecular weight approximately 20,000) as a water-soluble polymer.
Cerium nitrate as rare earth metal salt 0.02~0.2
Dry the aqueous solution containing 0 mol in an impregnation machine at 80℃ for 1 hour 50
Cerium oxide was dispersed and supported by heat treatment at 0°C for 30 minutes.Each gas seal member was immersed in an aqueous solution of chloroplatinic acid and then heat treated at a rolling speed (\0.1w of platinum).
The sealing performance of the obtained gas seal member was measured under the same conditions as in Example 1. The results are shown in Table 3.

(以下余白) 実施例4 かさ密度0.4g/cc、  厚み8mm(7)フルミ
ナシリカ繊維フェルトに水溶性高分子として ポリエチ
レングリコール(分子量的20000)10wt%と希
土類金属塩として硝酸セリウム含む水溶液を含浸機 8
0℃で1時間乾燥 500℃で30分間熱処理し 酸化
セリウムを分散担持させた その後塩化白金酸の水溶液
に浸漬し 転速熱処理を行1.%  白金を0.1wt
%担持したガスシール部材を実施例1と同様な条件でガ
スシール性を測定し九 それらの結果を表4に示す。
(Space below) Example 4 Flumina silica fiber felt with a bulk density of 0.4 g/cc and a thickness of 8 mm was impregnated with an aqueous solution containing 10 wt% of polyethylene glycol (molecular weight 20,000) as a water-soluble polymer and cerium nitrate as a rare earth metal salt. 8
Dry at 0°C for 1 hour, heat treat at 500°C for 30 minutes to disperse and support cerium oxide, then immerse in an aqueous solution of chloroplatinic acid and perform rotational heat treatment.1. % 0.1wt platinum
The gas sealing properties of the gas sealing member loaded with 9% of the gas loading were measured under the same conditions as in Example 1.The results are shown in Table 4.

表2、表3、表4の結果か収 ガラスシール部材として
はアルミナシリカ繊維に酸化セリウムを担持し 比表面
積2m2/g以上の時優れたシール性を示すことがわか
った しかし 担持する酸化セリウムが多くなると、ガ
スシール部材のクツション性(復元性)は急激に悪くな
り、触媒燃焼装置で燃詭 消火を繰り返した時燃焼体と
シール部材またはシール部材と枠体との間に隙間ができ
易くなり、初期においては優れた性能を示しているにも
かかわらず、寿命試験後にはガス漏れが生じた したが
って、本発明におけるガスシール部材のかさ密度は0.
15〜0. 50g/ccの範囲にするのが好まし鶏 
ここで、かさ密度0.15g/ccはガスシール部材の
強度を考慮した値であり、 これ以下のものでは充分な
強度がなく、使用に耐えな(ち な耘 本発明で使用する耐熱性無機繊維からなるシート
またはフェルトと(よ アルミナシリカ繊観 炭化珪素
繊観 窒化珪素繊維などの耐熱性を有する無機繊維から
なるものであればよい力(コストの観点から考え 現在
広い用途で使われているアルミナシリカ繊維がもっとも
好まししも またその組成としてはアルミナ40〜95
wt% シリカ5〜60wt%のものが好ましt〜 そ
の理由は耐熱性を考慮するならばアルミナ分を多くする
ことが好ましいのである力丈 アルミナ分を多くし過ぎ
ると繊維が脆くなってくるためである。またガスシール
部材のクツション法 機械的強度を考慮すると、繊維長
50mm以五 繊維径5μm以下の繊維からなゑ かさ
密度0.15〜0.40g / c c程度のシートま
たはフェルトを使用して希土類金属酸化物の担持を行う
ことが好ましl、%発明の効果 以上のように本発明によれ(L 次の効果が得られも (1)未燃焼ガスを触媒燃焼し 適度のクツション性を
有するガスシール部材が得られも   (2)燃焼体と
それを保持する枠体との隙間のガスシール部材より漏れ
る未燃焼成分を完全に防止できる燃焼装置が得えられ也
 特に高濃度の未燃焼成分を含む触媒燃焼装置では本発
明の効果が著しく〜
The results of Tables 2, 3, and 4 are summarized. Cerium oxide is supported on alumina-silica fiber as a glass sealing member, and it was found that excellent sealing performance was exhibited when the specific surface area was 2 m2/g or more. However, the supported cerium oxide If the amount increases, the cushioning properties (restoring properties) of the gas seal member will deteriorate rapidly, and gaps will easily form between the combustion body and the seal member, or between the seal member and the frame body, when repeatedly extinguishing a fire using a catalytic combustion device. Despite showing excellent performance in the initial stage, gas leakage occurred after the life test. Therefore, the bulk density of the gas seal member in the present invention is 0.
15-0. It is preferable to keep it in the range of 50g/cc.
Here, the bulk density of 0.15 g/cc is a value that takes into account the strength of the gas seal member, and anything less than this does not have sufficient strength and cannot be used (by the way) The heat-resistant inorganic fiber used in the present invention A sheet or felt made of heat-resistant inorganic fibers such as alumina, silica fibers, silicon carbide fibers, and silicon nitride fibers is suitable (from a cost perspective, alumina, which is currently used in a wide range of applications) Silica fiber is most preferred, and its composition is alumina 40-95.
Preferably 5 to 60 wt% silica.The reason for this is that if heat resistance is taken into consideration, it is preferable to increase the alumina content.Strength If the alumina content is too large, the fibers will become brittle. It is. In addition, considering the mechanical strength of the cushioning method for gas seal members, rare earth materials can be made using sheets or felts with a fiber length of 50 mm or more, a fiber diameter of 5 μm or less, and a bulk density of 0.15 to 0.40 g/cc. It is preferable to support a metal oxide.As described above, the present invention provides the following effects (1) Catalytic combustion of unburned gas and appropriate cushioning properties. (2) Even if a gas seal member is obtained, a combustion device can be obtained that can completely prevent unburned components leaking from the gas seal member in the gap between the combustion body and the frame that holds it. The effects of the present invention are remarkable in catalytic combustion devices including

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

第1図は本発明の一実施例によるガスシール部材を有す
る燃焼装置の断面医 第2図(A)、第2図(B)はそ
れぞれ実施例1、比較例3のシール部材の厚み方向にお
ける酸化セリウムの分散状態を分析した図であム ト・・ガスシール部材。 第2図 第 図 カスシール部材 摩り万βJ(mnう
FIG. 1 is a cross-sectional diagram of a combustion device having a gas seal member according to an embodiment of the present invention. FIG. 2 (A) and FIG. This is a diagram analyzing the dispersion state of cerium oxide. Gas seal member. Fig. 2 Fig. Cas seal member

Claims (3)

【特許請求の範囲】[Claims] (1)耐熱性無機繊維からなるシートまたはフェルトに
水溶性高分子と希土類金属塩を含む水溶液を含浸し、そ
の後乾燥、熱分解して希土類金属酸化物をシートまたは
フェルト中に分散担持させ、さらにその後白金族系金属
を担持させることを特徴とするガスシール部材の製造方
法。
(1) A sheet or felt made of heat-resistant inorganic fibers is impregnated with an aqueous solution containing a water-soluble polymer and a rare earth metal salt, and then dried and pyrolyzed to disperse and support the rare earth metal oxide in the sheet or felt. A method for manufacturing a gas seal member, which comprises subsequently supporting a platinum group metal.
(2)水溶性高分子がポリエチレングリコールであるこ
とを特徴とする請求項1記載のガスシール部材の製造方
法。
(2) The method for manufacturing a gas seal member according to claim 1, wherein the water-soluble polymer is polyethylene glycol.
(3)シートまたはフェルトが2m^2/g以上の比表
面積を有し、かつ0.15〜0.50g/ccのかさ密
度を有することを特徴とする請求項1記載のガスシール
部材の製造方法。
(3) Manufacturing the gas seal member according to claim 1, wherein the sheet or felt has a specific surface area of 2 m^2/g or more and a bulk density of 0.15 to 0.50 g/cc. Method.
JP2196602A 1990-07-24 1990-07-24 Manufacturing method of gas seal member Expired - Fee Related JP2858363B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2196602A JP2858363B2 (en) 1990-07-24 1990-07-24 Manufacturing method of gas seal member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2196602A JP2858363B2 (en) 1990-07-24 1990-07-24 Manufacturing method of gas seal member

Publications (2)

Publication Number Publication Date
JPH0481488A true JPH0481488A (en) 1992-03-16
JP2858363B2 JP2858363B2 (en) 1999-02-17

Family

ID=16360480

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2196602A Expired - Fee Related JP2858363B2 (en) 1990-07-24 1990-07-24 Manufacturing method of gas seal member

Country Status (1)

Country Link
JP (1) JP2858363B2 (en)

Also Published As

Publication number Publication date
JP2858363B2 (en) 1999-02-17

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