JPS6240053B2 - - Google Patents
Info
- Publication number
- JPS6240053B2 JPS6240053B2 JP53129467A JP12946778A JPS6240053B2 JP S6240053 B2 JPS6240053 B2 JP S6240053B2 JP 53129467 A JP53129467 A JP 53129467A JP 12946778 A JP12946778 A JP 12946778A JP S6240053 B2 JPS6240053 B2 JP S6240053B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- collection efficiency
- dust collection
- dust
- 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
Links
- 239000011347 resin Substances 0.000 claims description 41
- 229920005989 resin Polymers 0.000 claims description 41
- 239000000428 dust Substances 0.000 claims description 24
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 9
- 239000004925 Acrylic resin Substances 0.000 claims description 7
- 229920000178 Acrylic resin Polymers 0.000 claims description 7
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000004094 surface-active agent Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 229920003002 synthetic resin Polymers 0.000 claims description 2
- 239000000057 synthetic resin Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 8
- 239000004745 nonwoven fabric Substances 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 239000003945 anionic surfactant Substances 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- -1 butyl lauryl Chemical group 0.000 description 4
- 229920006026 co-polymeric resin Polymers 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000282320 Panthera leo Species 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 125000006487 butyl benzyl group Chemical group 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- SGGOJYZMTYGPCH-UHFFFAOYSA-L manganese(2+);naphthalene-2-carboxylate Chemical compound [Mn+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 SGGOJYZMTYGPCH-UHFFFAOYSA-L 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Filtering Materials (AREA)
Description
本発明は、防塵マスクなどのフイルター材を加
工するための含浸処理剤に関するものである。
従来、防塵マスク用などのフイルター材の処理
方法としては、羊毛フエルトのような材に合成
樹脂を含浸せしめた後、余分の液を絞り、100℃
程度に加熱乾燥して樹脂加工することにより、
材に静電気効果を付与する方法が広く採用されて
いた。
またその他、特公昭39−5987号「防塵マスクの
材処理方法」などを以つて従来方法の欠点を解
消した方法が提案されている。これはパラアルキ
ルフエノール類にホルマリンを加えた混合液に触
媒として塩酸と塩化アンモンの適量を加え加温し
て得られる溶液Aと、パラターシヤリブチルフエ
ノールにホルマリンを加えて得た混合液に触媒と
してアンモニア水の適量を加え加温して得られる
樹脂Bとを調整し、この溶液Aおよび樹脂Bをベ
ンゾールを適宜加え加温して得られる樹脂液に羊
毛フエルトのような材を浸漬乾燥することを特
徴とするものである。
しかし、公知方法はいずれも樹脂の溶剤として
上記したようにベンゾールなどの有機溶剤を使用
するため、この溶剤回収設備に多大の費用を必要
とするばかりでなく、火災や人災などの安全、衛
生の面でも種々の問題が残されていた。
これに対し、本発明者等は先に特願昭52−
34997号「防塵マスクなどのフイルター材の処理
方法」などを以つて、羊毛、不織布などの適宜の
材に公知手段による樹脂の含浸、乾燥処理を施
した後、引き続き機械的に曲げたり、伸ばした
り、手でもみほぐしたり、或いはこれらに類似の
物理的手段によるなめし加工処理を施し、公知の
ものに比べて、不織布のような安価な材や通気
抵抗の小さい他の材を用いても収塵効率を大幅
に向上し得る方法を提案した。
本発明は、この先願発明に適用させる含浸処理
剤に関するもので、樹脂を、水を溶剤とし、界面
活性剤を用いてエマルジヨン化することにより、
羊毛のように有機溶剤性の樹脂液でないと樹脂含
浸が困難とされていた材に対しても付着、含浸
性が良く、また前記した公知方法におけるような
高価な溶剤回収設備を必要とせず、さらに安全、
衛生面の欠点をも伴なわないで、収塵効率が大幅
に改善する防塵フイルターを製造することのでき
る含浸処理剤を提供するものである。
本発明における樹脂は、アクリル系樹脂、スチ
レン系樹脂、酢酸ビニール系樹脂の単独若しくは
混合物で、これらはホモ重合型樹脂、又は、アク
リルースチレン、アクリルー酢酸ビニール、スチ
レンー酢酸ビニール、エチレンー酢酸ビニールな
どの共重合型樹脂である。
また本発明における界面活性剤は乳化分散剤と
して用いられるもので、アニオン系、ノニオン系
のいずれも使用できるが、アクリル系樹脂やスチ
レン系樹脂に対しては特にアニオン系が効果的で
あり、酢酸ビニール系樹脂に対しては特にアニオ
ン系もしくはノニオン系が効果的であり、アクリ
ルー酢酸ビニール共重合型樹脂に対しては特にア
ニオン系が効果的である。
本発明において、樹脂の添加量は後述する参考
例に示すように防塵フイルターの収塵効率上0.3
〜2重量%とすることが重要であり、また界面活
性剤の添加量は樹脂添加量の1/10とする。
なお、本発明においては、必要に応じてナフテ
ン酸鉄、ナフテン酸マンガン、ナフテン酸コバル
ト、ナフテン酸亜鉛、クロム酸、クロム酸アルカ
リなどの硬化促進剤、ジメチルフタレート、ジエ
チルフタレート、ジイソブチルフタレート、ジブ
チルフタレート、ジヘブチルフタレート、ジオク
チルフタレートなどのフタル酸エステルやプチル
ベンジル、プチルラウリルなどのフタル酸混基エ
ステルなどの可塑剤等を添加してもよい。これら
の硬化促進剤や可塑剤等の添加により、本発明含
浸処理剤含浸後の硬化時間が短縮されたり、硬化
乾燥後の樹脂被膜の状態が改善されるなどの効果
が得られ、これによつて収塵効率に対する悪影響
は全く見られない。
更に、本発明においては、樹脂の乳化分散の安
定性を良くするために、アクリル系樹脂やスチレ
ン系樹脂の場合にはPH7〜8の弱アルカリ性に、
酢酸ビニール系樹脂の場合にはPH4〜5.5の弱酸
性とする必要がある。
以上説明した本発明の含浸処理剤は、1フエル
ト(天然動物性繊維)、2綿、レーヨンなどの天
然植物性繊維の織布または不織布、3ポリプロピ
レン、ポリオレフイン、ナイロン、アクリルなど
の合成繊維の単独もしくは組合せの不織布、4上
記3の合成繊維と上記2の天然植物性繊維との組
合せ不織布、5ゴム、ウレタンなどの発泡成形
品、などの各種の材に含浸させた後、ロールな
どによつて余分の液を絞り、100〜150℃程度に加
熱乾燥し、引き続き、このものを機械的に曲げた
り、伸ばしたり、手でもみほぐしたり、或いはこ
れに類似の物理的手段によるなめし処理を施すこ
とにより、通気性が良く、しかも収塵効率が極め
て高い防塵フイルターを製造することができるの
で、産業上極めて有益である。
以下、実施例により本発明をより具体的に説明
する。
実施例 1
粒子径0.5〜1μに調整した酢酸ビニール樹脂
2重量部を、アニオン系界面活性剤(ライオン油
脂社製商品名リポラン)0.2重量部、硬化促進剤
(ナフテン酸コバルト)0.5重量部、残部水よりな
る配合比のものに良く混合し、さらに酢酸を少量
添加してPHを5.5としたところ、やがてエマルジ
ヨン化して乳白色状を呈した。
このものを厚さ3mmのフエルト含浸後、ロール
によつて余分の液を絞り、50〜60℃に予備乾燥さ
せ、更に110℃の恒温槽中にて加熱乾燥した。引
き続きその一部は、10mmφのロールを15mm間隔
(ロールの中心から中心までの距離)にちどり状
に合計7本設置したなめし装置に3回通過させ、
他の一部はなめし装置を通過させることなくその
ままで防塵フイルターとなし、両者の収塵効率を
JIS T8151「防塵マスク」の試験方法に準じて測
定比較したところ、前者(なめし処理あり)は収
塵効率99.8%であるのに対し、後者(なめし処理
なし)は収塵効率54.5%であつた。
実施例 2
粒子径を0.1〜0.2μに調整したアクリル樹脂1.5
重量部、アニオン系界面活性剤(第一工業薬品社
製商品名ラベリン)0.15重量部、硬化促進剤(ナ
フテン酸コバルト)0.3重量部を水94.7重量部に
加え、苛性ソーダにてPHを7に調節してよく混
合、撹拌した。このものはやがてエマルジヨン化
して乳白色状を呈した。
このものをポリプロピレンとレーヨンの混綿か
らなる厚さ1.5mmの不織布を材とする以外は実
施例1と全く同様にしてなめし処理ありの防塵フ
イルターとし、実施例1と同様の収塵効率測定を
行なつたところ、2枚重ねで収塵効率99.8%であ
つた。
実施例 3
粒子径を0.1〜0.2μに調整したアクリルースチ
レン共重合型樹脂1重量部とアニオン系界面活性
剤(ライオン油脂社製商品名リポラン)0.1重量
部を水98重量部に加え、苛性ソーダにてPHを7.5
に調節したうえで良く混合、撹拌し、エマルジヨ
ン化せしめた。
このものをポリプロピレンとレーヨンの混綿か
らなる厚さ3.0mmの不織布を材とする以外は実
施例1と全く同様にしてなめし処理ありの防塵フ
イルターとし、実施例1と同様の収塵効率測定を
行なつたところ、2枚重ねで収塵効率99.8%であ
つた。
参考例
最適樹脂濃度を確認するため以下の種々の実験
を行なつた。
先ず、予備テストの結果、アクリル系樹脂、ス
チレン系樹脂、酢酸ビニール系樹脂のホモ重合型
樹脂又は共重合型樹脂の単独もしくは混合物につ
いては、樹脂の種類に関係なく同一濃度では略々
同等の収塵効率が得られることが判つた。
次いで、実施例1における酢酸ビニール樹脂を
用いて樹脂濃度を種々変えた以外は実施例1と全
く同様にしてエマルジヨン溶液をつくり、材と
してはポリプロピレンとレーヨンの混綿からなる
厚さ3mmと1.5mmの不織布を用い、それぞれにつ
いて実施例1と同様にしてなめし処理ありの防塵
フイルターとし、3mmのものと1.5mmのものとを
重ねた状態で実施例1と同様の収塵効率測定を行
なつた。結果は表1に示す通りであつた。
The present invention relates to an impregnation treatment agent for processing filter materials such as dust masks. Conventionally, the method of processing filter materials such as those for dust masks is to impregnate a material such as wool felt with synthetic resin, squeeze out the excess liquid, and heat it at 100°C.
By heating and drying to a certain degree and processing with resin,
A method of imparting an electrostatic effect to materials was widely adopted. In addition, other methods have been proposed, such as Japanese Patent Publication No. 39-5987 ``Method for Processing Materials for Dust Masks'', which eliminate the drawbacks of the conventional methods. Solution A is obtained by adding appropriate amounts of hydrochloric acid and ammonium chloride as a catalyst to a mixture of para-alkyl phenols and formalin, and heating the solution. A material such as wool felt is immersed in the resin solution obtained by adding an appropriate amount of ammonia water and heating it to prepare the resin B. A material such as wool felt is immersed in the resin solution obtained by adding appropriate amount of benzol and heating the solution A and resin B. It is characterized by this. However, all of the known methods use organic solvents such as benzene as the solvent for the resin, which not only requires a large amount of money for the solvent recovery equipment, but also poses safety and hygiene concerns such as fires and human disasters. Various problems still remained. In contrast, the present inventors previously filed a patent application filed in 1973-
No. 34997 "Method for processing filter materials such as dust masks" etc., after impregnating appropriate materials such as wool or non-woven fabric with resin and drying them by known means, mechanically bending or stretching the materials. Dust can be collected by hand-rubbing, tanning by similar physical means, and using cheaper materials such as non-woven fabrics or other materials with lower ventilation resistance than known methods. We proposed a method that can significantly improve efficiency. The present invention relates to an impregnating treatment agent applied to this prior invention, by emulsifying a resin using water as a solvent and a surfactant.
It has good adhesion and impregnation properties even for materials such as wool, which are difficult to impregnate with resin unless it is an organic solvent-based resin liquid, and does not require expensive solvent recovery equipment as in the above-mentioned known method. Even safer,
To provide an impregnating agent that can produce a dustproof filter with significantly improved dust collection efficiency without any hygienic drawbacks. The resin used in the present invention is an acrylic resin, a styrene resin, or a vinyl acetate resin, either alone or as a mixture. It is a copolymer resin. In addition, the surfactant in the present invention is used as an emulsifying dispersant, and both anionic and nonionic surfactants can be used, but anionic surfactants are particularly effective for acrylic resins and styrene resins, and acetic acid Anionic or nonionic resins are particularly effective for vinyl resins, and anionic resins are particularly effective for acrylic-vinyl acetate copolymer resins. In the present invention, the amount of resin added is 0.3 in terms of the dust collection efficiency of the dustproof filter, as shown in the reference example below.
It is important that the amount of surfactant be ~2% by weight, and the amount of surfactant added should be 1/10 of the amount of resin added. In addition, in the present invention, curing accelerators such as iron naphthenate, manganese naphthenate, cobalt naphthenate, zinc naphthenate, chromic acid, alkali chromate, dimethyl phthalate, diethyl phthalate, diisobutyl phthalate, dibutyl phthalate, etc. , plasticizers such as phthalic acid esters such as dihebutyl phthalate and dioctyl phthalate, and phthalic acid mixed group esters such as butyl benzyl and butyl lauryl. By adding these curing accelerators, plasticizers, etc., effects such as shortening the curing time after being impregnated with the impregnating treatment agent of the present invention and improving the condition of the resin film after curing and drying can be obtained. No adverse effect on dust collection efficiency was observed at all. Furthermore, in the present invention, in order to improve the stability of the emulsified dispersion of the resin, in the case of acrylic resins and styrene resins, a weak alkaline solution with a pH of 7 to 8,
In the case of vinyl acetate resin, it needs to be weakly acidic with a pH of 4 to 5.5. The impregnating treatment agent of the present invention described above can be applied to 1) felt (natural animal fiber), 2) woven fabrics or non-woven fabrics of natural vegetable fibers such as cotton and rayon, and 3) single fibers of synthetic fibers such as polypropylene, polyolefin, nylon, and acrylic. Alternatively, it can be impregnated into various materials such as a combination non-woven fabric, a combination non-woven fabric of the synthetic fibers described in 3 above and natural vegetable fibers described in 2 above, 5 foam molded products such as rubber or urethane, etc., and then rolled or the like. Squeeze out excess liquid, heat and dry at around 100-150℃, and then apply tanning treatment by mechanically bending, stretching, loosening by hand, or similar physical means. This makes it possible to manufacture a dustproof filter with good air permeability and extremely high dust collection efficiency, which is extremely useful industrially. Hereinafter, the present invention will be explained in more detail with reference to Examples. Example 1 2 parts by weight of vinyl acetate resin adjusted to a particle size of 0.5 to 1μ, 0.2 parts by weight of an anionic surfactant (product name: Liporan, manufactured by Lion Oil Co., Ltd.), 0.5 parts by weight of a curing accelerator (cobalt naphthenate), and the remainder When the mixture was well mixed with water and a small amount of acetic acid was added to adjust the pH to 5.5, it eventually turned into an emulsion and took on a milky white appearance. This product was impregnated with felt to a thickness of 3 mm, and the excess liquid was squeezed out using a roll, pre-dried at 50 to 60°C, and further heated and dried in a constant temperature bath at 110°C. Then, a part of it was passed three times through a tanning device with a total of seven rolls of 10 mm diameter installed in a chain at 15 mm intervals (distance from center to center of the rolls).
The other part is used as a dust filter without passing through the tanning equipment, improving the dust collection efficiency of both.
When compared according to the JIS T8151 "dust mask" test method, the former (with tanning treatment) had a dust collection efficiency of 99.8%, while the latter (without tanning treatment) had a dust collection efficiency of 54.5%. . Example 2 Acrylic resin 1.5 with particle size adjusted to 0.1-0.2μ
Add parts by weight, 0.15 parts by weight of an anionic surfactant (trade name: Labelin, manufactured by Dai-ichi Kogyo Yakuhin Co., Ltd.), and 0.3 parts by weight of a curing accelerator (cobalt naphthenate) to 94.7 parts by weight of water, and adjust the pH to 7 with caustic soda. Mix and stir well. This material eventually turned into an emulsion and took on a milky white appearance. This was made into a tanned dustproof filter in the same manner as in Example 1 except that the nonwoven fabric with a thickness of 1.5 mm made of a blend of polypropylene and rayon was used, and the dust collection efficiency was measured in the same manner as in Example 1. After getting used to it, the dust collection efficiency was 99.8% with two layers. Example 3 1 part by weight of an acrylic-styrene copolymer resin whose particle size was adjusted to 0.1 to 0.2μ and 0.1 part by weight of an anionic surfactant (product name: Riporan, manufactured by Lion Oil Co., Ltd.) were added to 98 parts by weight of water, and caustic soda was added. PH at 7.5
After adjusting the temperature, the mixture was thoroughly mixed and stirred to form an emulsion. This product was made into a tanned dustproof filter in the same manner as in Example 1 except that the material was a 3.0 mm thick nonwoven fabric made of a blend of polypropylene and rayon, and the dust collection efficiency was measured in the same manner as in Example 1. After getting used to it, the dust collection efficiency was 99.8% with two layers. Reference Example The following various experiments were conducted to confirm the optimum resin concentration. First, as a result of preliminary tests, homopolymer resins such as acrylic resins, styrene resins, and vinyl acetate resins, or copolymer resins alone or in mixtures, have approximately the same yield at the same concentration, regardless of the type of resin. It has been found that dust efficiency can be obtained. Next, an emulsion solution was prepared in exactly the same manner as in Example 1 except that the vinyl acetate resin used in Example 1 was used and the resin concentration was varied. Using non-woven fabric, each was made into a tanned dustproof filter in the same manner as in Example 1, and the dust collection efficiency was measured in the same manner as in Example 1 with a 3 mm filter and a 1.5 mm filter stacked one on top of the other. The results were as shown in Table 1.
【表】
表1から明らかなように、収塵効率は樹脂濃度
と密接な関係にあり、樹脂濃度に応じた収塵効率
が得られるが、JISに規定された1級防塵マスク
の規定値95%以上を得るためには樹脂濃度を0.3
〜2重量%の範囲内に保つことが必要であること
が判る。また、その理由については、付着する樹
脂量が少なくても多過ぎても静電効果が小さくな
るためと考えられる。[Table] As is clear from Table 1, the dust collection efficiency is closely related to the resin concentration, and the dust collection efficiency can be obtained according to the resin concentration. To obtain more than %, the resin concentration should be 0.3
It turns out that it is necessary to keep it within the range of ~2% by weight. Moreover, the reason for this is thought to be that the electrostatic effect becomes smaller whether the amount of resin attached is too small or too large.
Claims (1)
処理を行なつて防塵フイルターを製造するための
含浸処理剤において、0.3〜2重量%のアクリル
系樹脂、スチレン系樹脂、酢酸ビニール系樹脂の
単独若しくは混合物を含み、さらに残部水と上記
樹脂量の1/10の界面活性剤とを含むとともに、上
記樹脂がアクリル系樹脂、スチレン系樹脂の場合
にはPH7〜8の弱アルカリ性に、酢酸ビニール系
樹脂の場合にはPH4〜5.5の弱酸性にPH調整され
たことを特徴とする防塵フイルター用含浸処理
剤。1. In an impregnating treatment agent for manufacturing a dust filter by tanning by physical means after impregnating with a synthetic resin, 0.3 to 2% by weight of acrylic resin, styrene resin, or vinyl acetate resin alone or Contains a mixture, and further contains the balance water and a surfactant of 1/10 of the amount of the above resin, and if the above resin is an acrylic resin or a styrene resin, it is slightly alkaline with a pH of 7 to 8, and a vinyl acetate resin. In this case, an impregnating treatment agent for dust filters characterized by having a pH adjusted to a weak acidity of PH4 to 5.5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12946778A JPS5556814A (en) | 1978-10-23 | 1978-10-23 | Impregnated material for dust-preventing filter |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12946778A JPS5556814A (en) | 1978-10-23 | 1978-10-23 | Impregnated material for dust-preventing filter |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5556814A JPS5556814A (en) | 1980-04-26 |
JPS6240053B2 true JPS6240053B2 (en) | 1987-08-26 |
Family
ID=15010205
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12946778A Granted JPS5556814A (en) | 1978-10-23 | 1978-10-23 | Impregnated material for dust-preventing filter |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5556814A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58101721A (en) * | 1981-12-11 | 1983-06-17 | Toa Nenryo Kogyo Kk | Filter |
WO2000013764A1 (en) * | 1998-09-03 | 2000-03-16 | University Of Florida | Novel methods and apparatus for improved filtration of submicron particles |
-
1978
- 1978-10-23 JP JP12946778A patent/JPS5556814A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5556814A (en) | 1980-04-26 |
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