JPH03221142A - Adsorbent indicator - Google Patents
Adsorbent indicatorInfo
- Publication number
- JPH03221142A JPH03221142A JP19210489A JP19210489A JPH03221142A JP H03221142 A JPH03221142 A JP H03221142A JP 19210489 A JP19210489 A JP 19210489A JP 19210489 A JP19210489 A JP 19210489A JP H03221142 A JPH03221142 A JP H03221142A
- Authority
- JP
- Japan
- Prior art keywords
- indicator
- adsorbent
- filter
- activated carbon
- plastic
- 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
Links
- 239000003463 adsorbent Substances 0.000 title abstract description 33
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 35
- 238000001179 sorption measurement Methods 0.000 claims abstract description 25
- 229920003023 plastic Polymers 0.000 claims abstract description 12
- 239000004033 plastic Substances 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 238000000465 moulding Methods 0.000 claims abstract description 10
- 239000011230 binding agent Substances 0.000 claims abstract description 9
- 239000002184 metal Substances 0.000 claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 claims abstract description 9
- 239000000843 powder Substances 0.000 claims abstract description 9
- 150000003839 salts Chemical class 0.000 claims abstract description 6
- 239000004816 latex Substances 0.000 claims abstract description 5
- 229920000126 latex Polymers 0.000 claims abstract description 5
- 150000003464 sulfur compounds Chemical class 0.000 claims abstract 4
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract 3
- 150000004706 metal oxides Chemical class 0.000 claims abstract 3
- 238000002156 mixing Methods 0.000 claims description 14
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 8
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 claims 4
- 229910001923 silver oxide Inorganic materials 0.000 claims 2
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- 229920005989 resin Polymers 0.000 abstract description 23
- 239000011347 resin Substances 0.000 abstract description 23
- 239000002245 particle Substances 0.000 abstract description 13
- -1 salt compound Chemical class 0.000 abstract description 10
- 229920001187 thermosetting polymer Polymers 0.000 abstract description 5
- 229920005992 thermoplastic resin Polymers 0.000 abstract description 4
- RAOSIAYCXKBGFE-UHFFFAOYSA-K [Cu+3].[O-]P([O-])([O-])=O Chemical compound [Cu+3].[O-]P([O-])([O-])=O RAOSIAYCXKBGFE-UHFFFAOYSA-K 0.000 abstract description 3
- 239000005749 Copper compound Substances 0.000 abstract description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract description 2
- 239000005062 Polybutadiene Substances 0.000 abstract description 2
- 150000001880 copper compounds Chemical class 0.000 abstract description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 abstract description 2
- 150000002611 lead compounds Chemical class 0.000 abstract description 2
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 abstract description 2
- 229920002239 polyacrylonitrile Polymers 0.000 abstract description 2
- 229920002857 polybutadiene Polymers 0.000 abstract description 2
- 229910000365 copper sulfate Inorganic materials 0.000 abstract 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 16
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 16
- 238000000034 method Methods 0.000 description 16
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 12
- 239000007789 gas Substances 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000499 gel Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000004926 polymethyl methacrylate Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000010457 zeolite Substances 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 239000012744 reinforcing agent Substances 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 3
- 239000000779 smoke Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 241000208125 Nicotiana Species 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000011295 pitch Substances 0.000 description 2
- 229920001197 polyacetylene Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 229910001961 silver nitrate Inorganic materials 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000276425 Xiphophorus maculatus Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 229920001600 hydrophobic polymer Polymers 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000011302 mesophase pitch Substances 0.000 description 1
- 229910001510 metal chloride Inorganic materials 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は吸着剤フィルターや濾過体の寿命を簡単に知る
方法を提供することにある。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention provides a method for easily determining the lifespan of an adsorbent filter or a filter body.
吸着剤は種々7)分野で使用されているが、使用中に有
害物質を吸着し、性能は低下する。長期間夏用すると吸
着能が殆ど無くなって1ハるのに知らずに、使−用しそ
浄化効果が得られないということがよく起こる。従って
、これらをフィルターとして用いる場合に、吸着剤の残
存能力とマツチングした形でフィルターの寿命予測がで
きれば、フィルターの交換時期を明確にすることが可能
になり、著しく好ましい。Adsorbents are used in various fields, but during use they adsorb harmful substances and their performance deteriorates. If it is used for a long time in summer, it often loses its adsorption capacity and, without realizing it, the purifying effect is not obtained. Therefore, when these are used as filters, it is extremely preferable if the lifespan of the filter can be predicted by matching it with the residual capacity of the adsorbent, as this will make it possible to clarify when to replace the filter.
本発明は、吸着剤の有害物質対する残留吸着能に相関し
て変化するインディケータ−及び、これを内蔵すること
により、フィルターの交換時期をフィルターの残留吸着
能に対応して表示する方法を提供することにちる。The present invention provides an indicator that changes in correlation with the residual adsorption capacity of an adsorbent for harmful substances, and a method of displaying the filter replacement time in accordance with the filter's residual adsorption capacity by incorporating this indicator. Particularly.
吸着剤は一般家庭でも安易に使用されるようになったが
、長期間使用すると劣化が起こる。その際、吸着剤の性
能がどれだけ残留しているか正確にわからないという欠
点がある。Adsorbents have come to be easily used in ordinary households, but they deteriorate when used for a long period of time. In this case, there is a drawback that it is not possible to know exactly how much of the adsorbent's performance remains.
従来からよ〈行なわれている、フィルターの交換時期を
表示する方法としては、例えばフィルタ−@面に紙を張
りつけ、色の変化により寿命を予測する方法がある。こ
れはタバコの煙がくるとヤニで茶色′/Cなることを利
用したものである。しかし、この方法ではタバコ煙を含
まないガスの浄化ンご用いた場合、茶色への変色が起こ
らないので吸着剤が劣化していても指示されない事にな
る。A conventional method of indicating when to replace a filter is, for example, pasting paper on the filter surface and predicting the service life based on the change in color. This takes advantage of the fact that when cigarette smoke comes in, the resin turns brown/C. However, when this method is used to purify gas that does not contain tobacco smoke, no discoloration to brown occurs, so even if the adsorbent has deteriorated, it will not be indicated.
また、電池の電圧変化を利用して電池と豆球を用いる方
法があるが、点灯していると電力が消費され電池7)電
圧が低下すれば、豆球が消えることを利用したものであ
る。がこれは処理するガスの有害成分が高濃度であろう
が低濃度で多ろうが無関係に、一定期間が過き゛れば、
寿命の指示が出ることになり、きわめて不適当である。There is also a method of using a battery and a miniature bulb that takes advantage of changes in battery voltage, but this method takes advantage of the fact that when the light is on, power is consumed and if the battery voltage drops, the miniature bulb disappears. . However, regardless of whether the harmful components in the gas to be treated are high or low in concentration, once a certain period of time has passed,
This would be extremely inappropriate as it would give instructions on the lifespan.
あるいはカレンダーを張りつけ、時間が経過すれば取り
替えるなど、吸着剤の残留性能に無関係な指標を使用し
ている場合が多かった。この場合、使用しなくても時間
が来れば交換することになり、無駄である。Alternatively, indicators unrelated to the residual performance of the adsorbent were often used, such as attaching a calendar and replacing it after a certain period of time. In this case, even if you do not use it, you will have to replace it when the time comes, which is wasteful.
本来フィルターの寿命は、高濃度のガスが来れば垣時間
で劣化し、低#度のガスであれば長時間の寿命になるも
のである。従ってフィルターの寿命を表わすインディケ
ータ−としては、吸着剤の残留吸着能に応じて寿命を示
すものでなくてはならない。Normally, the lifespan of a filter is that if it is exposed to high-concentration gas, it will deteriorate within a short period of time, but if it is exposed to low-concentration gas, it will last for a long time. Therefore, as an indicator of filter life, it is necessary to indicate the life according to the residual adsorption capacity of the adsorbent.
吸着剤の残存性能と対応する形で使用期間、残存性能が
推定できれば、吸着剤が劣化すればその使用期間に関わ
らず寿命を指示できることになる。If the usage period and residual performance can be estimated in a manner that corresponds to the residual performance of the adsorbent, it will be possible to indicate the service life regardless of the usage period if the adsorbent deteriorates.
この様なインディケータ−及びそれを内蔵したフィルタ
ーは産業上、きわめて有効である。Such an indicator and a filter incorporating it are extremely effective industrially.
吸着剤の残留吸着能に対応してインディケータ−機能を
発揮する組成物を板状、円柱状、円筒状、ノート状に加
工して、インディケータ−として使用する方法によび、
ノイルター内にインディケータ−が内蔵可能なように成
型加工し、それを吸着剤と一体加工し、吸着剤の残存寿
命と関連した指標を提供することにある。By processing a composition that exhibits an indicator function in accordance with the residual adsorption capacity of an adsorbent into a plate shape, a cylinder shape, a cylindrical shape, or a notebook shape and using it as an indicator,
The purpose of the present invention is to mold the indicator so that it can be built into the noiler, integrate it with the adsorbent, and provide an index related to the remaining life of the adsorbent.
本発明のインディケータ−及びイ/デイケータ−を内蔵
した濾過体は以下の様にして得られる。A filter body incorporating an indicator and an indicator of the present invention can be obtained as follows.
以下、その具体豹な製、失について詳しく説明する。Below, we will explain in detail the specifics of how it was made and how it was made.
(1) インディケータ−の製法と性能■インディケ
ータ−の種類
本発明のインディケータ−は硫化水素用、アルデヒド用
すなわち、硫化水素用としては金属塩化合物−活性突系
が利用できる。硫化水素の累積吸Wtと対応したインデ
ィケータ−として利用できる。この場合、金TJX塩化
合物としては、各種金属化合物が使用可能であるが、燐
酸銅、硫酸鋼、塩化銅などの銅化合物や、硫酸鉛、蓚酸
鉛等の鉛化合物が好lしい。(1) Indicator manufacturing method and performance (1) Types of indicators The indicator of the present invention can be used for hydrogen sulfide or aldehyde, that is, for hydrogen sulfide, a metal salt compound-activated system can be used. It can be used as an indicator corresponding to the cumulative absorption Wt of hydrogen sulfide. In this case, various metal compounds can be used as the gold TJX salt compound, but copper compounds such as copper phosphate, steel sulfate, and copper chloride, and lead compounds such as lead sulfate and lead oxalate are preferred.
4た、硝酸銀を添着したアクリル酸ゲルや、活性炭では
アセトアルデヒドや、ホルマリンなどの、アルデヒド化
合物に対1−で、反応し°C銀を析出し、電気抵抗が低
下するので、アルデヒドセンサーとして使用可能である
。4.Acrylic acid gel impregnated with silver nitrate and activated carbon react with aldehyde compounds such as acetaldehyde and formalin in a 1-to-1 ratio to precipitate silver at °C and reduce electrical resistance, so they can be used as aldehyde sensors. It is.
インディケータ−の形状としては、より的確なセンシイ
ティビティを出すためには、円柱状、板状、線状、円筒
状など、有害成分との接触を妨げない形状が好ましい。In order to obtain more accurate sensitivity, the shape of the indicator is preferably a shape that does not prevent contact with harmful components, such as a columnar shape, a plate shape, a linear shape, or a cylindrical shape.
■インデイケーターの製法
本発明のインディケータ−は、硫化水素用、アルデヒド
用については、以下のようにして作ることができる。す
なわち、粒子径0.1〜50μの金属塩化物100部と
粒子径0.1〜50μの活性炭粉末を10〜1000部
の範囲でよく混合し成型して得られる。この金属塩と活
性炭の混合組成物を、その混合比率を変えることにより
、吸着量に対する感度を変化させることができる。すな
わち、金属塩の量が少ない場合は、小量の吸着量で変化
が大きく、多い場合は、多量に吸着しないと変化しない
インディケータ−が得られる。(2) Manufacturing method of indicator The indicator of the present invention for hydrogen sulfide and aldehyde can be manufactured as follows. That is, it is obtained by thoroughly mixing 100 parts of a metal chloride with a particle size of 0.1 to 50 μm and activated carbon powder with a particle size of 0.1 to 50 μm in a range of 10 to 1000 parts and molding the mixture. By changing the mixing ratio of this mixed composition of metal salt and activated carbon, the sensitivity to the amount of adsorption can be changed. That is, when the amount of metal salt is small, a small amount of adsorption causes a large change, and when it is large, an indicator is obtained that does not change unless a large amount is adsorbed.
これらの混合物を必要な形状に成形する必要があるが、
成形のためのバインダーとしては、ラテックスや、プラ
スチック粉末が使用できる。It is necessary to mold these mixtures into the required shape,
Latex or plastic powder can be used as a binder for molding.
ラテックスとしては、ポリアクリロニトリル、ポリブタ
ジェン、ボリアリレート、ポリ酢酸ビニル、カルボキシ
ルメチルセルローズ、メチルセルローズ等が使用可能で
ある。配合量は金g塩と活性炭の混合#J100部に対
して50〜100部になる。As the latex, polyacrylonitrile, polybutadiene, polyarylate, polyvinyl acetate, carboxylmethylcellulose, methylcellulose, etc. can be used. The blending amount is 50 to 100 parts per 100 parts of mixture #J of gold g salt and activated carbon.
グラスチックの粒子径は0.1〜100μ、好!しくば
5〜50μである。The particle size of glasstic is 0.1 to 100μ, which is good! The thickness is 5 to 50μ.
ここでグラスチックとは、熱可塑性樹脂、熱硬化性樹脂
、戎水性樹脂、導電性樹脂等を言う。Here, the term "glasstic" refers to thermoplastic resins, thermosetting resins, water-soluble resins, conductive resins, and the like.
熱可塑性樹脂としてはポリエチレ/、ポリプロピレン、
ABS、PET、ナイロン、PBT1エチレンアクリル
#4旨、PMMAJ14旨、メソ7エーズピツチ等が使
用9能である。Thermoplastic resins include polyethylene/, polypropylene,
ABS, PET, nylon, PBT1 ethylene acrylic #4, PMMAJ14, Meso7Aze pitch, etc. can be used.
熱硬化性樹脂としては7ラン樹脂、フェノールtM脂等
が使用可能である。As the thermosetting resin, 7 run resin, phenol tM resin, etc. can be used.
親水性樹脂としてはポリビニルアルコール樹脂、エバー
ル樹脂、等が使用可能である。As the hydrophilic resin, polyvinyl alcohol resin, EVAL resin, etc. can be used.
導電性樹脂としてはポリビニルピロール、ポリアセチレ
ノ等が使用可能である。As the conductive resin, polyvinylpyrrole, polyacetylene, etc. can be used.
補強剤
強度を向上させるためには、補強剤を入れても良い。補
強剤としては、ガラス繊維、炭素繊維、金属繊維などが
使用できる。II!維径は、0.1〜30μ、長さd
0.5〜10■が最適である。添加量は0.5〜10部
、好1しくは2〜5部である。Reinforcing agent In order to improve the strength, a reinforcing agent may be added. As the reinforcing agent, glass fiber, carbon fiber, metal fiber, etc. can be used. II! The fiber diameter is 0.1-30μ, length d
0.5 to 10 cm is optimal. The amount added is 0.5 to 10 parts, preferably 2 to 5 parts.
混合法
混合方法としては、通常の工業的混合方法、例えばミキ
サー リボンミキサー スタティックミキサー ボール
ミル、サンプルミル、ニーダ−等が使用できるがこの限
りでない。Mixing Method As the mixing method, ordinary industrial mixing methods such as mixers, ribbon mixers, static mixers, ball mills, sample mills, kneaders, etc. can be used, but are not limited to these methods.
成型法
押出成型、ロールプレス、ベレットミル、打錠成型など
の方法で、板状、円柱状、筒状が作れる。Molding method Platy, cylindrical, and cylindrical shapes can be made using methods such as extrusion molding, roll press, pellet mill, and tablet molding.
電気抵抗を検出するためのリード線は両端を金属溶射し
てそれに半田付けするか、予め成型の際、埋め込むか、
あるいは導電性の接着剤で接着するなどの方法が利用で
きる。The lead wire for detecting electrical resistance can be sprayed with metal at both ends and soldered to it, or can be embedded in the molding process beforehand.
Alternatively, a method such as bonding with a conductive adhesive can be used.
フィルター型枠内の所定の位置にインディケータ−のリ
ード線を出して、一体成形してもよい。The lead wire of the indicator may be brought out at a predetermined position within the filter mold frame and integrally molded.
リード線は、ステンレス線、鋼被覆線、エナメル線など
が使える。As the lead wire, stainless steel wire, steel coated wire, enameled wire, etc. can be used.
■インデイケーターの使用法
単独で用いる場合は、暴露量インディケータ−として利
用可能である。■How to use the indicator When used alone, it can be used as an exposure amount indicator.
(2)内蔵型フィルターの製法、性能
不イ/デイケータ−は吸着剤を含むノイルターと共に使
用することにより、そのフィルターの残留吸着能に対応
した形で電気抵抗の変化を取り出せるので、フィルター
の取り替え時期を適確に予測することができる。気相、
液相に使える。(2) Manufacturing method of built-in filter, performance failure/Decator can be used with Noilter containing an adsorbent to extract changes in electrical resistance in a form corresponding to the filter's residual adsorption capacity, so it is time to replace the filter. can be accurately predicted. gas phase,
Can be used in liquid phase.
概略の製法
インディケータ−がベレット状、筒状、円柱状であれば
、フィルター内部に入れることが可能である。板状であ
れば、フィルターの外枠として、底形する。If the general manufacturing method indicator is pellet-shaped, cylindrical, or cylindrical, it can be placed inside the filter. If it is plate-shaped, it will have a bottom shape as the outer frame of the filter.
フィルターに用いる吸着材としては、活性炭、ゼオライ
ト、シリカゲル、アルミナゲル等、なんでも使用可能で
ある。Any adsorbent can be used for the filter, such as activated carbon, zeolite, silica gel, alumina gel, etc.
ゼオライトでは、天然ゼオライト、合成ゼオライト、モ
vキ、 5− 、;/−7”5A、 3A、 4A、
13X。Zeolites include natural zeolite, synthetic zeolite, movki, 5-,;/-7"5A, 3A, 4A,
13X.
ZSM−5等いづれも使用可能である。ZSM-5 etc. can also be used.
本発明に用いる吸着材の粒度は使用目的に合致すればな
んでも良い。気相フィルターの場合、粒径、0.5−〜
5−が好筐しい。液相の場合Fii。The particle size of the adsorbent used in the present invention may be of any size as long as it meets the purpose of use. For gas phase filters, the particle size is 0.5-~
5- is good. Fii in case of liquid phase.
メフ、ツユ〜32メツ/ユが良い。が、これに限定され
るものではない。Mefu, tsuyu~32metsu/yu is good. However, it is not limited to this.
1ft、吸着剤の形状は破砕状、ペレット状、顆粒状あ
るいは′flta吠、ノエルト状、織物状、シート状な
どのいづA7)形態の吸着剤でも使用可能である。濾過
体として必要な形状であればよい。圧損及び入れ替えな
どの取扱状、造粒炭iたは、吸着剤を添着した7一ト状
吸着剤が便利な場合がある。1 ft. The adsorbent may be in the form of crushed, pellet, granule, or in the form of a sheet, cloth, cloth, etc.A7). It may have any shape as long as it is necessary as a filter. For handling such as pressure loss and replacement, granulated carbon or a 7-piece adsorbent with an adsorbent attached may be convenient.
〔接着材]
そのま1でも、バラでノイルターに充填してもよい。バ
インダーを用いてブロック状に成型してもよい。ブロッ
ク化した場合はインディケータ−を一体止できるメリッ
トがある。バインダーとして用いるプラスチ、りとして
は、熱可塑性グラスチック、メソ7エーズピツチ等、水
や有機溶剤を用いずに加熱融着できるものが適している
。[Adhesive] It may be used as is, or it may be filled into a neuter in bulk. It may be molded into a block shape using a binder. Blocking has the advantage of being able to block the indicators all at once. Suitable plastics to be used as the binder are those that can be heat-fused without using water or organic solvents, such as thermoplastic glass and meso-7A pitch.
本発明′/C使用するプラスチックは吸着剤表面に添着
した場合、着色性や接着哩、導電性を賦与し得るもので
もよい。The plastic used in the present invention'/C may be one that can impart colorability, adhesiveness, and conductivity when attached to the surface of the adsorbent.
更にグラスチック類を選択することKより、そ7)$質
と吸着剤との複合機能を付与できれば、更に新しい弔途
の展開が可能になる。ここでグラスチックとは、熱可塑
性樹脂、熱硬化性樹脂、親水性樹脂、導電性樹脂等を言
う。Furthermore, if a glass material can be selected, 7) If it can be given a composite function of a material and an adsorbent, it will become possible to develop even newer methods of condolence. Here, the term "glasstic" refers to thermoplastic resins, thermosetting resins, hydrophilic resins, conductive resins, and the like.
熟可塑性崗脂としてはポリエチレ/、ポリプロピレノ、
ABS、PET、ナイロン、PBT、エチレノアクリル
fIi脂、PMMA樹脂、メソフェーズピッチ等が使用
可能である。As mature plastic resin, polyethylene/, polypropyleno,
ABS, PET, nylon, PBT, ethylenenoacrylic fii resin, PMMA resin, mesophase pitch, etc. can be used.
熱硬化性樹脂としては7ラン樹脂、フェノール調脂等が
使用oT能である。As the thermosetting resin, 7 run resin, phenol fat control, etc. can be used.
親水性樹、指としてはポリビニルアルコール樹脂エバー
ルミ1脂、等が使用可能である。Hydrophilic resins such as polyvinyl alcohol resin Everumi 1 resin can be used for the fingers.
導電性樹脂としてはポリビニルビロール、ポリアセチレ
ン等が使用可能である。As the conductive resin, polyvinyl pyrrole, polyacetylene, etc. can be used.
これらの接着剤樹脂は、使用目的に応じて使い分けるの
が好ましい。すなわち、水溶液の吸着に用いる場合は親
水性ポリマーを接着剤とするのが最適で、また、油、有
機溶剤などのろ過に用いる場合は、疎水性ポリマーを接
着剤にするのが、その対象点物質に対する親和性の点で
好ましい。It is preferable to use different adhesive resins depending on the purpose of use. In other words, when used for adsorption of aqueous solutions, it is best to use hydrophilic polymers as adhesives, and when used for filtration of oils, organic solvents, etc., it is best to use hydrophobic polymers as adhesives. Preferable in terms of affinity for substances.
これらの粒子径としては、o、 i u m〜100
p m s好fしくは、5Pm〜50μmであるがこの
限りではない。These particle diameters are o, i u m ~ 100
Pms is preferably 5 Pm to 50 μm, but is not limited to this.
本発明のインディケータ−を内蔵したフィルターの製法
としては、吸着剤表面に予め、接着剤粉末をコーティン
グまたは付着させ、この吸着剤粒子と内蔵すべきインデ
ィケータ−を同時に所望の枠に内にいれ、加熱圧着する
事により、得られる。The method of manufacturing the filter containing the indicator of the present invention is to coat or adhere adhesive powder to the surface of the adsorbent in advance, place the adsorbent particles and the indicator to be incorporated into a desired frame at the same time, and heat the filter. Obtained by crimping.
バインダーの粒子径としてはN lpm−100Pm
1好1しくは、57Am 〜50pmであるカコの限り
ではない。The particle size of the binder is N lpm-100Pm
Preferably, the range is not limited to 57 Am to 50 pm.
吸着材に対する接着剤の使用割合は、吸着材の粒度や比
重によって異なるが、吸着材100重量部に対して、プ
ラスチツク2〜lO重量部が好ましいが、必要最低限で
あることが、吸着能低下を防ぐ点から良い。The ratio of the adhesive to the adsorbent varies depending on the particle size and specific gravity of the adsorbent, but it is preferably 2 to 10 parts by weight of plastic to 100 parts by weight of the adsorbent, but it is recommended to use the minimum necessary amount to prevent a decrease in adsorption capacity. Good in terms of preventing.
添着する方法は、混合することにより添着できるが、そ
の混合方法としては、通常の工業的混合方法、例えばミ
キサー リボンミキサー スタティックミキサー ボー
ルミル、サンプルミル、ニーダ−等が使用できるがこの
限りでない。混合の際、混合のみでも付着させることが
できるが、プラスチックと吸着材の接着をより強固にす
るために、簡単な加熱を行なうのがよい。熱源としては
静電気の発生下あるいは、マイクロ波、赤外線、遠赤外
線、高周波等を混合の際、同時に照射することにより、
より強固にできるが、これらを用いなくても良い。又加
熱の際、減圧下で加熱することにより、接着剤から発生
する低沸点有機化合物が吸着剤に吸着されて吸着能が低
下するのを防止することができる。成形圧力を大きくす
ることにより、強實の大きい酸型体が得られる。The impregnation can be carried out by mixing, and the mixing method may be a conventional industrial mixing method such as a mixer, ribbon mixer, static mixer, ball mill, sample mill, kneader, etc., but is not limited to this. At the time of mixing, adhesion can be achieved by mixing alone, but in order to strengthen the adhesion between the plastic and the adsorbent, it is better to perform simple heating. As a heat source, under the generation of static electricity or by simultaneously irradiating microwave, infrared rays, far infrared rays, high frequency, etc. during mixing,
Although it can be made stronger, it is not necessary to use these. Furthermore, by heating under reduced pressure during heating, it is possible to prevent low boiling point organic compounds generated from the adhesive from being adsorbed by the adsorbent, thereby preventing the adsorption capacity from decreasing. By increasing the molding pressure, a highly strong acid type body can be obtained.
これを空気清浄器のノイルターとして、専楽番使用する
ことにより、その寿命を適
確指示することができる。By using this as a noirter in an air purifier and using a dedicated number, it is possible to accurately indicate its lifespan.
単独で用いれり、sitインディケータ−として、また
、フィルターに内蔵するとそのフィルターの寿命を知ら
せることが出来、残留吸着能と対応して、寿命全知るこ
とができる。以下実施例によって、具体的な効果につい
て説明する。When used alone, it can be used as a sit indicator, and when incorporated into a filter, it can indicate the life of the filter, and in correspondence with the residual adsorption capacity, the entire life can be known. Specific effects will be explained below using Examples.
実施例 l
粉末活性炭100重量部シよび、燐酸鋼100重量部分
よび、粒子径30μmのポリエチレ/扮末35部をよく
混合し、これを板状(10■×50園xl論試料1)、
ペレット状(5ss*x30■試料2)、筒状内径(2
m*x外径6m*X20m試料3)に加熱加圧成形した
。これらの両端にステンレスの針金のり−ド111iを
取り付けた。!た粉末活性炭100重量部にたいして、
燐酸銅200重量部(試料4))よび、燐酸w4300
重量部(試料5))よび粒子径30μmのポリエチレン
粉末35部をよく混合し、これを板状(10■×50■
×1■)に成型した。Example l 100 parts by weight of powdered activated carbon, 100 parts by weight of phosphoric acid steel, and 35 parts of polyethylene powder with a particle size of 30 μm were thoroughly mixed, and this was prepared into a plate (10 x 50 x 1 theoretical sample 1).
Pellet (5ss*x30■sample 2), cylindrical inner diameter (2
Sample 3) with m*x outer diameter of 6 m*x20 m was molded under heat and pressure. Stainless steel wire glue 111i was attached to both ends of these. ! For 100 parts by weight of powdered activated carbon,
200 parts by weight of copper phosphate (sample 4)) and phosphoric acid w4300
parts by weight (sample 5)) and 35 parts of polyethylene powder with a particle size of 30 μm were mixed well, and this was prepared into a plate shape (10×50 μm).
×1■).
図1は各センサーの電気抵抗の経時変化である。Figure 1 shows the change in electrical resistance of each sensor over time.
図のように本発明のインディケータ−は、硫化水素の暴
gtに応じて電気抵抗は変化し、寿命インディケータ−
として、有効であることが明らかになった。As shown in the figure, the electric resistance of the indicator of the present invention changes depending on the extreme gt of hydrogen sulfide, and the life indicator changes.
It has been shown to be effective.
実施例 2
吸水倍率100倍のPMMAゲル10グラムを、硝酸*
5gを含む水1リットル中に投入し、吸水させて、硝!
1銀t−5Q wt %含むPMMAゲルを得た。これ
を直径lO■の円柱状に押し出し成型し、150℃5時
間乾燥して、直径約5■の硝酸銀含浸ゲルを得た。(試
料6)
この両端にリードiIAを取り付け、硫化水素吸着量イ
ノデイケータ−として用いた。Example 2 10 grams of PMMA gel with a water absorption rate of 100 times was dissolved in nitric acid*
Pour it into 1 liter of water containing 5g, let it absorb water, and make nitrate!
A PMMA gel containing 1 silver t-5Q wt % was obtained. This was extruded into a cylindrical shape with a diameter of 10 cm and dried at 150°C for 5 hours to obtain a silver nitrate-impregnated gel with a diameter of about 5 cm. (Sample 6) Lead iIA was attached to both ends of this sample and used as a hydrogen sulfide adsorption amount indicator.
図2に、硫化水素吸着量と電気抵抗の関係を示す。FIG. 2 shows the relationship between the amount of hydrogen sulfide adsorption and electrical resistance.
図のように本発明のPMMAゲル−硝酸銀成形体は、硫
化水素吸着量インディケータ−として使用可能である。As shown in the figure, the PMMA gel-silver nitrate molded article of the present invention can be used as a hydrogen sulfide adsorption amount indicator.
実施例3
硝酸#120重量部、活性炭粉末20重量部、粒子径2
0μのポリプコビレン粉末10重量部をよ〈混合し、こ
れを板状10■×50−×1謹(試料7)に加熱成形し
た。Example 3 Nitric acid #120 parts by weight, activated carbon powder 20 parts by weight, particle size 2
10 parts by weight of 0μ polypcopylene powder was thoroughly mixed, and the mixture was heated and molded into a plate shape of 10×50×1 size (sample 7).
実施例1と同じ方法で、アセトアルデヒドガスを2dづ
つ導入した。この時のインディケータ−の電気抵抗変化
を図3に示す。In the same manner as in Example 1, acetaldehyde gas was introduced 2 d at a time. FIG. 3 shows the change in electrical resistance of the indicator at this time.
図のように本発明のアルデヒドインディケータ−は、ア
ルデヒド吸着1に対応したインディケータ−となり得る
ことがよくわかる。As shown in the figure, it can be clearly seen that the aldehyde indicator of the present invention can be an indicator corresponding to aldehyde adsorption 1.
実施例 4
実施例1で作成した硫化水素インディケータ−試料1、
試料2、試料3を用いて硫化水素インデイケーターを内
蔵した空気清浄器用フィルターを作成した。Example 4 Hydrogen sulfide indicator sample 1 prepared in Example 1,
Using Samples 2 and 3, an air purifier filter with a built-in hydrogen sulfide indicator was created.
板状センサー(試料l)は、フィルターの枠の一部とし
て、使用し、ベレット状センサー(試料2)はベレット
状活性炭と共に、フィルター内部に充填した。筒状セン
サー(試料3)は、風の流れる方向に穴を向けてフィル
ター内にセフ)した。The plate-shaped sensor (sample 1) was used as part of the frame of the filter, and the pellet-shaped sensor (sample 2) was filled inside the filter together with pellet-shaped activated carbon. The cylindrical sensor (Sample 3) was placed inside the filter with the hole facing the direction of the wind flow.
このフィルターの大きさは、17国X19cmx9mで
活性炭の充填量′/180gであった。この活性炭の使
用前の硫化水素吸着量は28a6であった。The size of this filter was 17 mm x 19 cm x 9 m, and the amount of activated carbon charged was '/180 g. The hydrogen sulfide adsorption amount of this activated carbon before use was 28a6.
このフィルターを入れた空気清浄器を内容積1立方米の
箱に入れて、硫化水素を連続的に注入し、各センサーの
電気抵抗の変化を測定した。The air purifier containing this filter was placed in a box with an internal volume of 1 cubic meter, hydrogen sulfide was continuously injected, and changes in the electrical resistance of each sensor were measured.
図4はフィルターに置ける各センサーの設置状態、図5
は各センサーの電気抵抗の経時変化である。図のように
本発明のフィルターは、フィルターの硫化水素の処理量
に応じて電気抵抗は変化し、寿命センサーとして、有効
であることが明らかになった。Figure 4 shows the installation status of each sensor that can be placed on the filter, Figure 5
is the change in electrical resistance of each sensor over time. As shown in the figure, the electrical resistance of the filter of the present invention changes depending on the amount of hydrogen sulfide processed by the filter, making it clear that it is effective as a life sensor.
このときの使用済活性炭の硫化水素吸着量は、3.0%
であった。At this time, the amount of hydrogen sulfide adsorbed by the used activated carbon was 3.0%.
Met.
比較のため、寿命インディケータ−として用いた豆球点
灯式のインディケータ−では豆球の使用時間が短いため
、灯が消えなかった。For comparison, in the case of a light bulb type indicator used as a lifespan indicator, the light did not go out because the light bulb was used for a short time.
1fc便用腸始時にラベルを剥した白い紙は、白いtt
で変化が無かった。これは処理ガスがタバコ煙でないた
めである。The white paper from which the label was removed at the beginning of the 1fc stool is white tt.
There was no change. This is because the processing gas is not tobacco smoke.
この様に従来からあるインディケータ−は、フィルター
の吸着剤の残存性能と無@係な値指示を与えることがわ
かる。It can thus be seen that the conventional indicators give value indications that are independent of the residual performance of the adsorbent in the filter.
実施例 5
実施例3で作成したアルデヒドインディケータ−を実施
例4と同様にフィルターに成型し、実施例4と同じ方法
で、アセトアルデヒドガスft2dづつ導入した。この
時のインディケータ−の電気抵抗変化を図6に示す。Example 5 The aldehyde indicator prepared in Example 3 was molded into a filter in the same manner as in Example 4, and acetaldehyde gas ft2d was introduced in the same manner as in Example 4. FIG. 6 shows the change in electrical resistance of the indicator at this time.
このフィルターに充填した活性炭の使用前のアセトアル
デヒド吸着量は5wt%で、使用後の活性炭のアセトア
ルデヒド吸着量ばQ、2vt%であった。The amount of acetaldehyde adsorbed by the activated carbon filled in this filter before use was 5 wt%, and the amount of acetaldehyde adsorbed by the activated carbon after use was Q, 2 vt%.
図のように本発明のインディケータ−内蔵フィルターは
、アセトアルデヒド吸着能に対応した寿命を指示し得る
ことがわかる。As shown in the figure, it can be seen that the filter with a built-in indicator of the present invention can indicate the lifespan corresponding to the acetaldehyde adsorption capacity.
図1 実施例1、硫化水素吸着量と電気抵抗の関係 図2 実施例2、硫化水素吸着量と電気抵抗の関係 図3 実施例3、アルデヒド吸着量と電気抵抗の関係 図4 図5 図6 実施例4、 実施例4、 実施例5、 エアーフイルメーとインデイ ケータ−配置図 フィルター使用時間とインデ イケータ−の電気抵抗の関係 フィルター使用時間とインデ イケータ−の電気抵抗の関係 Figure 1 Example 1, relationship between hydrogen sulfide adsorption amount and electrical resistance Figure 2 Example 2, relationship between hydrogen sulfide adsorption amount and electrical resistance Figure 3 Example 3, relationship between aldehyde adsorption amount and electrical resistance Figure 4 Figure 5 Figure 6 Example 4, Example 4, Example 5, Air Film and Inday caterer layout plan Filter usage time and index Icator electrical resistance relationship Filter usage time and index Icator electrical resistance relationship
Claims (3)
ックスまたはプラスチック粉末をバインダーとして成型
せしめてなる悪臭硫黄化合物の吸着量インディケーター
。(1) An adsorption amount indicator for malodorous sulfur compounds made by mixing metal salts or metal oxides with activated carbon and molding the mixture with latex or plastic powder as a binder.
ゲルに含有せしめてなる悪臭硫黄化合物の吸着量インデ
ィケーター。(2) An adsorption amount indicator for malodorous sulfur compounds obtained by incorporating silver salt or silver oxide into a polymetal methacrylate gel.
またはプラスチック粉末をバインダーとして成型せしめ
てなるアルデヒド吸着量インディケーター。(3) An aldehyde adsorption amount indicator made by mixing silver salt or silver oxide with activated carbon and molding the mixture using latex or plastic powder as a binder.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19210489A JPH03221142A (en) | 1989-07-24 | 1989-07-24 | Adsorbent indicator |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19210489A JPH03221142A (en) | 1989-07-24 | 1989-07-24 | Adsorbent indicator |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03221142A true JPH03221142A (en) | 1991-09-30 |
Family
ID=16285725
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19210489A Pending JPH03221142A (en) | 1989-07-24 | 1989-07-24 | Adsorbent indicator |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03221142A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005039656A1 (en) * | 2003-10-16 | 2005-05-06 | Kimberly-Clark Worldwide, Inc. | Odor controlling article including a visual indicating device for monitoring odor absorption |
| WO2009055200A3 (en) * | 2007-10-26 | 2009-07-30 | Schlumberger Services Petrol | Downhole spectroscopic hydrogen sulfide detection |
| CN103566876A (en) * | 2013-09-26 | 2014-02-12 | 蚌埠华纺滤材有限公司 | Hydrogen-sulfide-removed modified active carbon and preparation method thereof |
| US9052289B2 (en) | 2010-12-13 | 2015-06-09 | Schlumberger Technology Corporation | Hydrogen sulfide (H2S) detection using functionalized nanoparticles |
| JP2017001187A (en) * | 2015-06-04 | 2017-01-05 | 共同印刷株式会社 | Laminate for sulfide-based gas adsorption |
-
1989
- 1989-07-24 JP JP19210489A patent/JPH03221142A/en active Pending
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005039656A1 (en) * | 2003-10-16 | 2005-05-06 | Kimberly-Clark Worldwide, Inc. | Odor controlling article including a visual indicating device for monitoring odor absorption |
| WO2009055200A3 (en) * | 2007-10-26 | 2009-07-30 | Schlumberger Services Petrol | Downhole spectroscopic hydrogen sulfide detection |
| US7959864B2 (en) | 2007-10-26 | 2011-06-14 | Schlumberger Technology Corporation | Downhole spectroscopic hydrogen sulfide detection |
| US8058071B2 (en) | 2007-10-26 | 2011-11-15 | Schlumberger Technology Corporation | Downhole spectroscopic hydrogen sulfide detection |
| US8518702B2 (en) | 2007-10-26 | 2013-08-27 | Schlumberger Technology Corporation | Downhole spectroscopic hydrogen sulfide detection |
| US9052289B2 (en) | 2010-12-13 | 2015-06-09 | Schlumberger Technology Corporation | Hydrogen sulfide (H2S) detection using functionalized nanoparticles |
| CN103566876A (en) * | 2013-09-26 | 2014-02-12 | 蚌埠华纺滤材有限公司 | Hydrogen-sulfide-removed modified active carbon and preparation method thereof |
| JP2017001187A (en) * | 2015-06-04 | 2017-01-05 | 共同印刷株式会社 | Laminate for sulfide-based gas adsorption |
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