JPH0669668B2 - Improved method for removing coatings from easily scratchable substrates and jetting media useful therefor - Google Patents
Improved method for removing coatings from easily scratchable substrates and jetting media useful thereforInfo
- Publication number
- JPH0669668B2 JPH0669668B2 JP3510591A JP51059191A JPH0669668B2 JP H0669668 B2 JPH0669668 B2 JP H0669668B2 JP 3510591 A JP3510591 A JP 3510591A JP 51059191 A JP51059191 A JP 51059191A JP H0669668 B2 JPH0669668 B2 JP H0669668B2
- Authority
- JP
- Japan
- Prior art keywords
- bicarbonate
- medium
- particle size
- hydrophobic silica
- microns
- 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
Links
- 238000000576 coating method Methods 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 16
- 239000000758 substrate Substances 0.000 title description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical group [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 48
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 46
- 239000002245 particle Substances 0.000 claims description 33
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 25
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 24
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 24
- 239000000377 silicon dioxide Substances 0.000 claims description 21
- 230000002209 hydrophobic effect Effects 0.000 claims description 18
- 239000002131 composite material Substances 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 5
- 125000005372 silanol group Chemical group 0.000 claims description 4
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 3
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- -1 alkali metal bicarbonate Chemical class 0.000 claims description 3
- 235000012538 ammonium bicarbonate Nutrition 0.000 claims description 3
- 239000001099 ammonium carbonate Substances 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 3
- 238000005422 blasting Methods 0.000 claims description 2
- 239000003112 inhibitor Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 description 10
- 239000003973 paint Substances 0.000 description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 6
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 238000005498 polishing Methods 0.000 description 5
- 239000003380 propellant Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000005488 sandblasting Methods 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000003082 abrasive agent Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 230000000069 prophylactic effect Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000011256 aggressive treatment Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010438 granite Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C7/00—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts
- B24C7/0084—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts the abrasive material being fed in a mixture of liquid and gas
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C1/00—Methods for use of abrasive blasting for producing particular effects; Use of auxiliary equipment in connection with such methods
- B24C1/08—Methods for use of abrasive blasting for producing particular effects; Use of auxiliary equipment in connection with such methods for polishing surfaces, e.g. smoothing a surface by making use of liquid-borne abrasives
- B24C1/086—Descaling; Removing coating films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C11/00—Selection of abrasive materials or additives for abrasive blasts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C11/00—Selection of abrasive materials or additives for abrasive blasts
- B24C11/005—Selection of abrasive materials or additives for abrasive blasts of additives, e.g. anti-corrosive or disinfecting agents in solid, liquid or gaseous form
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C7/00—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts
- B24C7/0046—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts the abrasive material being fed in a gaseous carrier
- B24C7/0053—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts the abrasive material being fed in a gaseous carrier with control of feed parameters, e.g. feed rate of abrasive material or carrier
- B24C7/0061—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts the abrasive material being fed in a gaseous carrier with control of feed parameters, e.g. feed rate of abrasive material or carrier of feed pressure
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Paints Or Removers (AREA)
- Cleaning By Liquid Or Steam (AREA)
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Description
【発明の詳細な説明】 発明の分野 この発明は、易傷性金属及び複合材の表面又は同様な基
体からの被膜除去法とそれに有用な噴射媒体に関する。Description: FIELD OF THE INVENTION The present invention relates to methods for removing coatings from surfaces of fragile metals and composites or similar substrates and jetting media useful therein.
発明の背景 建築物から工業用装置にわたって変化する各種の構造物
や装置の表面から被膜(コーティング)を洗浄又は除去
することが望まれることが多い。このような目的のため
多数の技術が知られており、塗料、シール剤、ラッカー
などのような表面被膜を洗浄又は除去に機械的研磨から
化学品の応用まである。花崗岩の壁や重質スチールメッ
キのような硬い耐久性表面は、サンドブラストのような
激しい研磨技法で洗浄又は剥離できる。よりデリケート
な表面は、基体損傷を防ぐため侵略性の少ない処理が必
要とされる。BACKGROUND OF THE INVENTION It is often desirable to wash or remove coatings from the surfaces of various structures and devices that vary from buildings to industrial equipment. A number of techniques are known for this purpose, ranging from mechanical polishing to chemical applications for cleaning or removing surface coatings such as paints, sealants, lacquers and the like. Hard and durable surfaces such as granite walls and heavy steel plating can be cleaned or stripped with vigorous polishing techniques such as sandblasting. More delicate surfaces require less aggressive treatment to prevent substrate damage.
民間の航空会社や軍当局は、近代的な飛行機の外面から
塗料や他の被膜を定期的に剥離又は研磨するのに多くの
金を消費している。これら表面は、軽量アルミ又は他の
金属合金、又は複合材からなり、これらは比較的柔かで
あり、塗料や他の被覆は、過剰の研磨や化学的損傷を避
けて注意して除去する必要がある。このような損傷は、
極端な場合に機械的破損になりうる。Civil aviation and military authorities spend a lot of money routinely stripping or polishing paint and other coatings from the exterior of modern aircraft. These surfaces are made of lightweight aluminum or other metal alloys, or composites, which are relatively soft, and paints and other coatings need to be carefully removed to avoid excessive polishing and chemical damage. There is. Such damage
In extreme cases mechanical damage can occur.
易傷性金属及び複合材の航空機などの表面からの被膜の
除去に、サンドブラストに類似の各種の改良剥離技術が
提案されている。このような目的に有用な噴射媒体(bl
asting media)は、次の基準に合致するのが好まし
い。Various improved stripping techniques similar to sandblasting have been proposed for the removal of coatings from vulnerable metal and composite surfaces such as aircraft. A jetting medium useful for such purposes (bl
asting media) preferably meets the following criteria:
1.比較的に非侵略性であること(モース硬度が約2.0〜
3.0)、 2.異なる基材の処理用に各種の粒度分布が入手可能であ
ること、 3.高湿度条件下、広範囲の空気圧と媒体流速で易流動性
であること、 4.剥離した不溶性塗料や樹脂の分離を容易にし廃棄物処
理を容易にする水溶性で非公害のものであること。1. Be relatively non-invasive (Mohs hardness is about 2.0 ~
3.0), 2. Various particle size distributions are available for the treatment of different substrates, 3. Free-flowing under high humidity conditions over a wide range of air pressures and medium flow rates, 4. Exfoliated insoluble paint Water-soluble and non-polluting, which facilitates the separation of resin and resin and facilitates waste disposal.
カーの米国特許第4,731,125号(1988年3月15日付与)
には、易傷性金属、複合材の表面の噴射洗浄用にプラス
チック媒体の使用が記載されている。しかし、このよう
な材料は比較的高価であり、その使用は廃棄物処理問題
を起こしうる。Car US Patent No. 4,731,125 (Granted March 15, 1988)
Describes the use of plastic media for jet cleaning of easily scratchable metal, composite surfaces. However, such materials are relatively expensive and their use can cause waste disposal problems.
航空機パーツのような易傷性表面から被膜を除去するた
めの噴霧媒体として重炭酸ナトリウムも提案されてい
る。重曹は、上記の基準1,2及び4に容易に合致するた
め、このような媒体の理想的な選択となる。かくして、
このものは比較的に非侵略性(モース硬度約2.5)であ
り、各種の粒子サイズが入手可能であり、水溶性があっ
て、アルカリ度やpHの調整用に汚水処理施設を処理する
のに通常利用されている。重炭酸ナトリウムのマイルド
な研磨特性は、例えば歯の研磨材で既に利用されてい
る。例えば米国特許第3,882,638号、第3,972,123号、第
4,174,571号、第4,412,402号、第4,214,871号、第4,46
2,803号、第4,482,322号、第4,487,582号、第4,492,575
号、第4,494,932号及び第4,522,597号参照。Sodium bicarbonate has also been proposed as a spray medium for removing coatings from vulnerable surfaces such as aircraft parts. Baking soda easily meets the criteria 1, 2 and 4 above, making it an ideal choice for such media. Thus,
It is relatively non-invasive (Mohs hardness about 2.5), is available in various particle sizes, is water soluble, and is suitable for treating wastewater treatment plants for alkalinity and pH adjustment. It is usually used. The mild abrasive properties of sodium bicarbonate are already utilized in tooth abrasives, for example. For example, U.S. Pat.Nos. 3,882,638, 3,972,123,
No. 4,174,571, No. 4,412,402, No. 4,214,871, No. 4,46
No. 2,803, No. 4,482,322, No. 4,487,582, No. 4,492,575
See Nos. 4,494,932 and 4,522,597.
重炭酸ナトリウムを噴射媒体として使用するに伴う主な
欠点は、圧縮又はより重要なのは高湿度条件下にさらさ
れることの何れかによりケーク化する傾向があることで
ある。これは市販の噴射仕上操作で激しく、その圧縮空
気流は実質的に湿気で飽和されており、すなわち90%以
上の相対湿度を有し、エヤーコンプレッサーからの油性
汚物を含んでいる。加えて、市販の重炭酸ナトリウム
は、通常の粒子サイズ分布と結晶形のため本質的に流動
特性が悪い。The major drawback with using sodium bicarbonate as the propellant medium is its tendency to cake, either by compression or, more importantly, by exposure to high humidity conditions. This is violent in commercial jet finishing operations, the compressed air stream is substantially saturated with moisture, that is, it has a relative humidity of 90% or more and contains oily debris from the air compressor. In addition, commercially available sodium bicarbonate inherently has poor flow properties due to the usual particle size distribution and crystalline form.
重炭酸ナトリウムの流動と凝結防止性を改良するために
流動助剤を添加することが知られている。かくして、パ
ン焼き用処方や歯科用エヤージェット予防媒体で重炭酸
ナトリウムにリン酸カルシウム(TCP)を配合すること
が以前提案されている。このような材料の添加は重炭酸
塩の流動と凝結防止特性を改良する。しかし、TCP処理
の重炭酸ナトリウムは、室温下で3〜6ケ月の貯蔵性で
あり、これはTCPが飽和まで湿気を吸収し、その後製品
が凝結するからである。It is known to add flow aids to improve the flow and anti-caking properties of sodium bicarbonate. Thus, it has previously been proposed to incorporate sodium bicarbonate with calcium phosphate (TCP) in a baking recipe or a dental air jet prophylaxis medium. The addition of such materials improves the bicarbonate flow and anti-caking properties. However, TCP treated sodium bicarbonate is storable at room temperature for 3 to 6 months because TCP absorbs moisture to saturation and then the product sets.
従って、この発明の目的は、重炭酸ナトリウム含有の噴
射媒体(blasting media)の提供と、このような媒体
を易傷性(sensitive)金属、複合材の表面からの被膜
除去に利用する方法を提供することにある。利用しうる
重炭酸塩噴射媒体は易流動性であり、悪い商業用噴射条
件下で長い貯蔵期限を有しており、かつ高湿で、広範囲
のよく調節された高流速及び空気圧下で噴射媒体として
利用できる。この発明の他の目的と利点は、次の好まし
い形態の記述から明らかであろう。Accordingly, it is an object of the present invention to provide a blasting media containing sodium bicarbonate and a method of using such media to remove coatings from the surface of sensitive metals and composites. To do. Bicarbonate jetting media available are free-flowing, have a long shelf life under poor commercial jetting conditions, and are humid, jetting media under a wide range of well-controlled high flow rates and air pressures. Available as Other objects and advantages of the invention will be apparent from the following description of the preferred embodiments.
発明の要約 この発明によれば、噴射媒体として、平均粒子サイズが
約100〜500ミクロン、好ましくは250〜300ミクロンの範
囲内を有する結晶性水溶性重炭酸ナトリウム粒子を、こ
の重炭酸塩の重量に対し、少なくとも約0.2%、好まし
くは約0.2〜3%の疏水性シリカの流動/凝結防止剤と
の混合で含有する約10〜150psiの圧力下の高速流動流、
望ましは実質的に飽和圧縮空気流で易傷性表面を噴射仕
上げすることからなる易傷性基体からの被膜除去方法を
提供する。SUMMARY OF THE INVENTION According to the present invention, crystalline water-soluble sodium bicarbonate particles having an average particle size in the range of about 100 to 500 microns, preferably 250 to 300 microns are used as the jetting medium in the weight of the bicarbonate salt. A high flow rate stream under pressure of about 10 to 150 psi, containing at least about 0.2%, preferably about 0.2 to 3% of hydrophobic silica mixed with a flow / anti-caking agent,
Desirably, there is provided a method of coating removal from a vulnerable substrate which comprises jet finishing the vulnerable surface with a substantially saturated stream of compressed air.
比較的大きな粒子サイズの重炭酸塩が、基体を損傷する
ことなく基体から腐食副産物ならびに他の被膜を除去す
るのに全く効果的であることが見い出された。これは、
噴射媒体として有効表面面積がより大きい小さな粒子が
大きな粒子より、より効果的な洗浄剤であるとの通常の
知識と矛盾する。その上、殆どの公知の噴射適用では、
噴霧材の供給速度が早い程、生産率がより高い、すなわ
ち被膜の除去がより早い。しかし、上記の粒子の大きさ
内の結晶性重炭酸塩を使用すると、効率的には0.5イン
チ直径のノズルを用いる通常のサンドブラスト装置で1
分当り約3〜4ポンドの供給量で経済的な生産率を達す
ることができる。この速度以下では、重炭酸塩噴射媒体
の供給速度を著しく高めても生産率の増加は殆どない。It has been found that the relatively large particle size of bicarbonate is quite effective in removing corrosion by-products as well as other coatings from the substrate without damaging the substrate. this is,
Contradictory with the common knowledge that small particles with a larger effective surface area as a jetting medium are more effective cleaning agents than large particles. Moreover, in most known injection applications,
The faster the feed rate of the spray material, the higher the production rate, ie the faster the removal of the coating. However, the use of crystalline bicarbonate within the above particle size effectively results in a conventional sandblasting machine with a 0.5 inch diameter nozzle.
Economic production rates can be reached with a supply of about 3-4 pounds per minute. Below this speed, the production rate hardly increases even if the supply rate of the bicarbonate injection medium is significantly increased.
この発明のもう1つの特徴によれば、噴射媒体に疏水性
シリリカの添加により、流動助剤を含まないか又はTCP
もしくは親水性シリカのような流動助剤を含む比較媒体
より有意に良好な流動特性が出る。加えて、重炭酸塩噴
射媒体で疏水性シリカ流動助剤を含むものは、有意に長
く、実質的に不定の保存期限を有し、商業用の圧縮空気
流の高い相対湿度で優れた耐性を奏する。According to another characteristic of the invention, the addition of hydrophobic silica to the propellant medium does not include flow aids or TCP
Alternatively, it provides significantly better flow properties than comparative media containing flow aids such as hydrophilic silica. In addition, bicarbonate jet media containing hydrophobic silica flow aids have significantly longer, substantially indefinite shelf life and excellent resistance to high relative humidity of commercial compressed air streams. Play.
この発明の噴射媒体で研磨材として結晶性重炭酸ナトリ
ウムを使用するのが好ましい。しかし、他の水溶性重炭
酸塩、例えば重炭酸カリウムのような重炭酸アルカリ金
属や重炭酸アンモニウムも同様に使用しうることも意図
される。従って、次の記述は、好ましい結晶性重炭酸ナ
トリウム含有噴射媒体について言及されるが、この発明
は他の水溶性結晶性重炭酸塩研磨材を含有する噴射媒体
も同様に包含されると理解されるであろう。It is preferred to use crystalline sodium bicarbonate as the abrasive in the jetting medium of this invention. However, it is contemplated that other water soluble bicarbonates, such as alkali metal bicarbonates such as potassium bicarbonate and ammonium bicarbonate may be used as well. Therefore, while the following description refers to preferred crystalline sodium bicarbonate-containing jetting media, it is understood that this invention also includes jetting media containing other water-soluble crystalline bicarbonate abrasives as well. Will
疏水性シリカは、歯科予防用の研磨媒体での流動助剤と
して親水性シリカとの混合で使用されていた。このよう
な媒体は、商業用噴射媒体と劇的に異なる条件下で適用
される。かくして、歯科予防用媒体は、約65〜75ミクロ
ンの粒子サイズを有する重炭酸塩粒子を含有し、約50〜
100psiの圧力下でクリーンの実験室的圧縮空気供給機の
圧力下、1/16〜1/32インチノズルを通して、分当り約3g
の割合で適用される。Hydrophobic silica has been used in admixture with hydrophilic silica as a flow aid in dental prophylactic polishing media. Such media are applied under conditions that are dramatically different than commercial jet media. Thus, the dental prophylactic medium contains bicarbonate particles having a particle size of about 65-75 microns and contains about 50-
Approximately 3g per minute through a 1/16 to 1/32 inch nozzle under the pressure of a clean laboratory compressed air supply under 100psi pressure
Applied in proportion.
最も重要なことは、このような空気供給機は湿気で実質
的に飽和されておらず、かつ、飽和圧縮空気噴射流中高
い押出量で商業用噴射媒体を適用する際の固有のものか
ら異なった流動とケーク化の問題がある。Most importantly, such air feeders are not substantially saturated with moisture and differ from those inherent in applying commercial jet media at high extrusion rates in saturated compressed air jets. There are problems of fluidity and cake.
この発明の噴射媒体は、疏水性シリカ粒子の混合で、結
晶性水溶性重炭酸塩、例えば重炭酸ナトリウムから本質
的になるものである。公知の親水性シリカと異なり疏水
性シリカは、非水素結合したシラノール基と吸収水とを
実質に含まない。The jetting medium of the present invention consists essentially of a crystalline water-soluble bicarbonate salt, such as sodium bicarbonate, with a mixture of hydrophobic silica particles. Unlike known hydrophilic silica, hydrophobic silica does not substantially contain non-hydrogen-bonded silanol groups and absorbed water.
噴射媒体に利用できる1つの好ましい疏水性シリカはエ
ロジル(Aerosil)R972で、デグーサ(Degussa)AGより
入手可能な製品である。このものは、純粋な凝結シリコ
ーンジオキシドエヤロゾルで、その表面のシラノール基
の約75%がジメチルジクロロシランと化学的に反応して
おり、その製品は、100m2表面積当り約0.7mmolの化学的
に結合したメチル基を有し、約1%の炭素を含有する。
その粒子は、約10〜40ナノメーターの間の直径で変動
し、約110m2/gの比表面積を有する。このものは親水性
シリカの火焔加水分解で作ることができる。より詳細に
はAngew.Chem.72,744(1960)、F-PS1,368,765及びDT−
AS1,163,784に記載されている。さらにこれらの材料に
関する詳細は、1986年8月デグーサACの技報の“エロジ
ルの基本的な特性と適用”に含まれている。One preferred hydrophobic silica that can be used in the jetting medium is Aerosil R972, a product available from Degussa AG. It is a pure coagulated silicone dioxide aerosol with about 75% of its surface silanol groups chemically reacting with dimethyldichlorosilane and the product is about 0.7 mmol of chemical per 100 m 2 surface area. It has a methyl group attached to and contains about 1% carbon.
The particles range in diameter between about 10-40 nanometers and have a specific surface area of about 110 m 2 / g. It can be made by flame hydrolysis of hydrophilic silica. More specifically Angew.Chem. 72, 744 (1960) , F-PS1,368,765 and DT-
AS 1,163,784. Further details regarding these materials are contained in the August 1986 Degussa AC Technical Report, "Basic Properties and Applications of Elosil".
疏水性シリカ粒子は、結晶性重炭酸ナトリウム噴射体
に、少なくとも約0.2%かつ約3%(重量)までの割合
で混合される。結晶性重炭酸塩粒子は、約100〜500ミク
ロンの範囲内の何れの所望の平均粒子サイズであっても
よい。噴射媒体が航空機外面のペイントの除去に利用さ
れるとき、約250〜300ミクロンの平均粒子サイズを有す
る結晶性重炭酸粒子を利用するのが好ましい。The hydrophobic silica particles are admixed with the crystalline sodium bicarbonate propellant at a rate of at least about 0.2% and up to about 3% (by weight). The crystalline bicarbonate particles can be any desired average particle size in the range of about 100 to 500 microns. When the jetting medium is utilized to remove paint on the exterior of an aircraft, it is preferred to utilize crystalline bicarbonate particles having an average particle size of about 250-300 microns.
このように構成された噴射媒体は、航空機外面のよう
に、易傷性金属、例えばアルミニウム又はアルミニウム
金属、又は複合材の基体を洗浄もしくは脱被膜化するの
に有用である。この噴射媒体で処理できる複合材は、マ
トリックス、例えばエポキシ樹脂で強化用のガラススト
ランド、グラファイトなどの繊維を含んでよいものから
なる。Jet media constructed in this manner are useful for cleaning or decoating fragile metals, such as aluminum or aluminum metal, or composite substrates, such as aircraft exterior surfaces. The composite material which can be treated with this jetting medium consists of a matrix, for example glass strands for reinforcement with epoxy resins, which may contain fibers such as graphite.
このような噴射媒体は、商業用圧縮空気流、すなわち、
実質的に湿気で飽和(90%又はそれ以上の相対湿度)さ
れ、コンプレッサーからの油汚物を含む流に適用するの
が好ましい。水流を、媒体/空気流に加えて、加工物を
冷却し、ダスト形成を調節することができるが、被膜除
去率はいくらか減少する。重炭酸塩/疏水性シリカ噴射
媒体は、1分当り約1〜10ポンド、望ましくは約3〜4
ポンドの流量で、1/4インチ又はそれより大きい噴射ノ
ズルから約10〜150psiの空気圧で適用できる。Such a propellant medium is a commercial compressed air stream, i.e.
It is preferably applied to streams that are substantially saturated with moisture (90% or higher relative humidity) and that contain oil fouling from the compressor. A water stream can be added to the media / air stream to cool the work piece and control dust formation, but the coating removal rate is somewhat reduced. The bicarbonate / hydrophobic silica jet medium is about 1-10 pounds per minute, preferably about 3-4.
Applicable at a flow rate of lbs and air pressure of about 10-150 psi from a 1/4 inch or larger injection nozzle.
この発明によれば、上記及び下記より詳しく示されるよ
うに、上記のように構成し、使用される噴射媒体は、ケ
ーク化せず、優れた保存期限を有し、易流動性である。
従って、このものは、易傷性金属及び複合材の表面から
被膜を除去するため商業用噴射作業で容易に使用できる
ものである。According to the invention, as will be shown in more detail above and below, the jetting medium configured and used as described above is not caked, has an excellent shelf life and is free-flowing.
Therefore, it is easy to use in commercial spraying operations to remove coatings from the surface of vulnerable metals and composites.
図面の簡単な説明 図1は表面に可視腐食を有し、クラッドを浸透している
クラッドアルミニウムテストパネルの噴射仕上げ前の電
子走査顕微鏡写真である。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is an electron scanning micrograph of a clad aluminum test panel having visible corrosion on the surface and infiltrating the clad before spray finishing.
図2は、この発明の方法によって洗浄されたクラッドア
ルミニウムテストパネルの電子走査顕微鏡写真である。
腐食副産物が、金属表面を損傷することなく除去された
ことが明らかである。FIG. 2 is an electron scanning micrograph of a clad aluminum test panel cleaned by the method of the present invention.
It is clear that the corrosion by-products were removed without damaging the metal surface.
図3は、異なる平均粒子サイズを有する重炭酸塩噴射媒
体を供給量を変えて使用して得られた生産速度を比較す
るグラフである。FIG. 3 is a graph comparing production rates obtained using bicarbonate jetting media having different average particle sizes at varying feed rates.
好ましい具体例の詳述 次の実施例は、この発明の噴射媒体についての易流動特
性(実施例1)、高生産速度(実施例2と3)を例証す
る。実施例で、特に示さない限り、全ての部とパーセン
トは重量で、全ての湿度は゜Fである。Detailed Description of the Preferred Embodiments The following examples illustrate the free-flowing properties (Example 1), high production rates (Examples 2 and 3) for the jetting media of the present invention. In the examples, all parts and percentages are by weight and all humidity are degrees Fahrenheit unless otherwise noted.
実施例1 2種の結晶性重炭酸ナトリウム試料(各々は約250〜300
ミクロンの平均粒子サイズを有し)、その内1つはエロ
ジルR-972疏水性シリカを0.5%混合したものを、標準サ
ンドブラスト装置で媒体として用いた。装置は、米国、
テキサス州、ヒューストンのシュミット社製のシュミッ
トアキュストリップシステムで、6方フートブラストポ
ットと800cfmコンプレッサーに連結させた0.5インチノ
ズル直径とトンプソンバルブを有する。ブラストポット
は、平均流量が測定できるようなスケールで装備され
た。Example 1 Two crystalline sodium bicarbonate samples (each about 250-300)
It had an average particle size of micron), one of which was a 0.5% blend of Elosil R-972 hydrophobic silica used as medium in a standard sandblasting machine. The equipment is
The Schmidt Acustrip system from Schmidt, Houston, Tex., Has a 6-way foot blast pot and a 0.5 inch nozzle diameter and a Thompson valve connected to an 800 cfm compressor. The blast pot was equipped with a scale such that the average flow rate could be measured.
各重炭酸塩製剤は、湿気飽和の室温の圧縮空気を利用
し、ブラストポットの噴射媒体を通過するよう60psig圧
でノズルを通して噴射された。Each bicarbonate formulation utilized compressed air at room temperature, which was saturated with moisture, and was sprayed through a nozzle at 60 psig pressure through the spray media of the blast pot.
疏水性シリカ流動助剤のない結晶性重炭酸ナトリウム粒
子は、間欠的にシステムを流動、ノズルの急速な目詰を
来たし、更なる流動を妨げた。補給した流動は保持でき
なかった。Crystalline sodium bicarbonate particles without hydrophobic silica flow aid intermittently flowed through the system, causing rapid nozzle clogging and impeded further flow. The replenished flow could not be maintained.
結晶性重炭酸塩−疏水性シリカ製剤は、1分当り1ポン
ドから5ポンドに変化する調節しうるレートで、65時間
以上システムを連続的に流動した。これによる流動問題
はみられなかった。The crystalline bicarbonate-hydrophobic silica formulation flowed through the system continuously for over 65 hours at an adjustable rate varying from 1 pound to 5 pounds per minute. There was no flow problem due to this.
実施例2 2フィート×2フィート×0.032インチ厚みのアルミニ
ウムのテストパネルを水で処理し、リン酸液で洗浄し、
水でリンスし、アロデン腐食防止剤を用い、最終の水リ
ンスでリンスして清浄化した。エポキシドプライマーを
塗布し、パネルを8時間風乾燥した。次いで、ポリウレ
タン塗料を塗布し、パネルを7日間乾燥した。次いで、
210゜Fの空気オーブン中で96時間熟成した。塗料とプ
ライマーのターゲット厚みは2ミリであった。Example 2 A 2 foot x 2 foot x 0.032 inch thick aluminum test panel was treated with water and washed with phosphoric acid solution,
Rinse with water, clean with alloden corrosion inhibitor, final water rinse. The epoxide primer was applied and the panel was air dried for 8 hours. The polyurethane paint was then applied and the panel dried for 7 days. Then
Aged in a 210 ° F. air oven for 96 hours. The target thickness of the paint and primer was 2 mm.
各種の重炭酸ナトリウム噴射媒体をその流量を規制する
適当なオリフィスプレートを備えたプラストポットに入
れた。噴射媒体は、99.5%の重炭酸ナトリウム(粒子サ
イズを異にし)と0.5%エロジルE972疏水性シリカから
なる。ノズル圧を60psiにセットし、媒体を所望供給量
を与えるのに十分な差圧にした。水圧は200psiの圧に
し、0.5gal/minの流動とした。加工物で作ったブラスト
ノズル角を60゜にセットした。媒体供給量を2から4
bs/minに変えた。Various sodium bicarbonate propellants were placed in a plasto pot equipped with a suitable orifice plate to regulate its flow rate. The jetting medium consists of 99.5% sodium bicarbonate (different particle size) and 0.5% Elosil E972 hydrophobic silica. The nozzle pressure was set to 60 psi and the medium was at a pressure differential sufficient to give the desired feed rate. The water pressure was 200 psi and the flow rate was 0.5 gal / min. The blast nozzle angle made of the work piece was set to 60 °. Medium supply from 2 to 4
changed to bs / min.
パネルの完全に脱ペイント化される時間を記録した。The time for the panel to be completely depainted was recorded.
各媒体での重炭酸塩の生産速度と平均粒子サイズは次の
通りであった。The bicarbonate production rate and average particle size for each medium were as follows:
このデータは、図3で要約され、曲線1が2bs/min、
曲線2が3b/min、曲線3が4b/minである。 This data is summarized in Figure 3, curve 1 at 2 bs / min,
Curve 2 is 3 b / min and curve 3 is 4 b / min.
このデータは重炭酸ナトリウムの大きな平均粒子サイズ
(150と250ミクロン)を用いる媒体が小さな粒子を含有
するものより全ての供給量でより効果的であることを示
す。This data shows that media using large average particle sizes of sodium bicarbonate (150 and 250 microns) are more effective at all feed rates than those containing small particles.
1分当り約3ポンドの平均流量で経済的な生産が達せら
れ、高い供給量では生産速度の改善が殆どないことも明
らかである。It is also clear that economic production is achieved with an average flow rate of about 3 pounds per minute, with little improvement in production rate at high feed rates.
実施例3 平均粒子サイズ約250〜300ミクロンの結晶性重炭酸ナト
リウムとエロジルR-972疏水性シリカ0.5%を混合してな
る実施例1記載の噴射媒体を、粒子が−20メッシュ〜+
40メッシュの範囲である圧縮重炭酸塩を同じ疏水性シリ
カ助剤の同様な量(0.5%)と混合してなる噴射媒体と
比較した。それぞれの媒体を、実施例2に記載と同じよ
うにアルミニウムテストパネルの脱ペイント化に用い
た。各媒体で得られた最大の生産速度を測定し、下記の
表とする。表は、圧縮重炭酸ナトリウムを入れた媒体よ
り結晶性重炭酸ナトリウムを入れた噴射媒体を用いた方
が生産速度の改良があることを示す。Example 3 An injection medium as described in Example 1 is prepared by mixing crystalline sodium bicarbonate having an average particle size of about 250 to 300 microns and 0.5% of Elosil R-972 hydrophobic silica.
Compressed bicarbonate, in the range of 40 mesh, was compared to a jetting medium mixed with a similar amount (0.5%) of the same hydrophobic silica aid. Each media was used to depaint aluminum test panels as described in Example 2. The maximum production rate obtained for each medium is measured and is given in the table below. The table shows that there is an improvement in production rate with the injection media containing crystalline sodium bicarbonate over the media containing compressed sodium bicarbonate.
上記の開示から、この発明が易傷性(鋭敏性)基体の表
面からペイント又は他の被膜を洗浄又は除去する方法と
それに有用な結晶性重炭酸ナトリウム含有噴射媒体を提
供するものであることが理解されるであろう。上記の好
ましい具体例で例示したプラスト工程と噴射媒体で、発
明の範囲を離れることなく各種の変形がなし得ることは
理解されるであろう。従って前の記述は例証であって、
限定されるものではないと解すべきである。 From the above disclosure, it is believed that the present invention provides a method of cleaning or removing paint or other coatings from the surface of a vulnerable (sensitized) substrate and a crystalline sodium bicarbonate-containing jetting medium useful therein. Will be understood. It will be appreciated that the plast process and jetting medium illustrated in the preferred embodiment above may be modified in various ways without departing from the scope of the invention. Therefore, the preceding description is illustrative,
It should be understood that it is not limited.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 スパイヤース、ウィリアム、イー.、ジュ ニアー 米国、テキサス 77043、ヒューストン、 トリウエイ 1927 ─────────────────────────────────────────────────── ─── Continued Front Page (72) Inventors Speyers, William, E. United States, Texas 77043, Houston, Triway 1927
Claims (9)
炭酸アンモニウムからなる群より選択された水溶性で結
晶性重炭酸塩粒子で、その重炭酸塩粒子の平均粒子サイ
ズが100〜500ミクロンであるものと該重炭酸塩に対して
0.2〜3重量%の疏水性シリカとを含有する高速流動流
で易傷性表面をブラストすることからなる易傷性金属、
複合材の表面からの被膜除去方法。1. Water-soluble crystalline bicarbonate particles selected from the group consisting of alkali metal bicarbonate and ammonium bicarbonate as the jetting medium, the bicarbonate particles having an average particle size of 100 to 500 microns. For things and the bicarbonate
A vulnerable metal comprising blasting a vulnerable surface with a high velocity flow stream containing 0.2 to 3% by weight of hydrophobic silica,
A method for removing a coating from the surface of a composite material.
飽和された圧縮空気流である請求項1の方法。2. The method of claim 1 wherein the flow stream is a substantially saturated compressed air stream under a pressure of 10 to 150 psi.
ポンドの割合で処理表面に適用される請求項1の方法。3. The jet stream has 1 to 10 bicarbonate particles per minute.
The method of claim 1 applied to the treated surface at a rate of pounds.
の平均粒子サイズを有する請求項1の方法。4. The method of claim 1 wherein the bicarbonate particles have an average particle size in the range of 250-300 microns.
1の方法。5. The method of claim 1 wherein the bicarbonate is sodium bicarbonate.
と吸収水を実質的に含まないものである請求項1の方
法。6. The method of claim 1 wherein the hydrophobic silica is substantially free of non-hydrogen bonded silanol groups and absorbed water.
からなる群より選択された水溶性で結晶性重炭酸塩粒子
で、その粒子サイズが100〜500ミクロンのものと、疏水
性シリカの流動/凝結防止材の重炭酸塩に対し0.2〜3
%(重量)との混合で本質的になる易傷性金属、複合材
の表面からの被膜除去用噴射媒体。7. Water-soluble crystalline bicarbonate particles selected from the group consisting of alkali metal bicarbonate and ammonium bicarbonate, having a particle size of 100-500 microns, and the flow / condensation of hydrophobic silica. 0.2 to 3 against bicarbonate as an inhibitor
% Fragile metal which becomes essentially by mixing with (weight), a jetting medium for removing a coating from the surface of a composite material.
リカが非水素結合シラノール基と吸収水を実質的に含ま
ない請求項7の噴射媒体。8. The jet medium of claim 7, wherein the bicarbonate is sodium bicarbonate and the hydrophobic silica is substantially free of non-hydrogen bonded silanol groups and absorbed water.
均粒子サイズを有する請求項7の噴射媒体。9. The jet medium of claim 7, wherein the bicarbonate salt has an average particle size in the range of 250 to 300 microns.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50644790A | 1990-04-06 | 1990-04-06 | |
| US506,447 | 1990-04-06 | ||
| PCT/US1991/002338 WO1991015308A1 (en) | 1990-04-06 | 1991-04-04 | Improved process for removing coatings from sensitive substrates, and blasting media useful therein |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05504919A JPH05504919A (en) | 1993-07-29 |
| JPH0669668B2 true JPH0669668B2 (en) | 1994-09-07 |
Family
ID=24014633
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3510591A Expired - Fee Related JPH0669668B2 (en) | 1990-04-06 | 1991-04-04 | Improved method for removing coatings from easily scratchable substrates and jetting media useful therefor |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0525122A4 (en) |
| JP (1) | JPH0669668B2 (en) |
| KR (1) | KR960003113B1 (en) |
| CN (1) | CN1029599C (en) |
| AU (1) | AU643039B2 (en) |
| CA (1) | CA2079892C (en) |
| MY (1) | MY109653A (en) |
| NO (1) | NO176751C (en) |
| NZ (1) | NZ237596A (en) |
| PL (1) | PL165174B1 (en) |
| TR (1) | TR25589A (en) |
| WO (1) | WO1991015308A1 (en) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5232514A (en) * | 1991-10-10 | 1993-08-03 | Church & Dwight Co., Inc. | Corrosion-inhibiting cleaning systems for aluminum surfaces, particularly aluminum aircraft surfaces |
| WO1993018863A1 (en) * | 1992-03-20 | 1993-09-30 | Church & Dwight Company, Inc. | Abrasive coating remover and process for using same |
| US5593339A (en) * | 1993-08-12 | 1997-01-14 | Church & Dwight Co., Inc. | Slurry cleaning process |
| NL1003398C2 (en) * | 1996-06-21 | 1997-12-23 | Delwi Ontwikkelingen B V | Passage-wall cleaning system using granular material |
| US6010546A (en) * | 1997-07-24 | 2000-01-04 | Asahi Glass Company, Ltd. | Blasting medium and blasting method employing such medium |
| NL1007501C2 (en) * | 1997-11-10 | 1999-05-11 | Pieter Schurink | Cleaning surfaces by blasting to remove e.g. dirt, scale or paint |
| DE19842054A1 (en) | 1998-09-15 | 2000-03-16 | Bayer Ag | Use of water-soluble polymeric polycarboxylates in cleaning formulations with an abrasive effect |
| DE19842053A1 (en) | 1998-09-15 | 2000-03-23 | Bayer Ag | Use of polyaspartic acids in cleaning formulations with an abrasive effect |
| GB2565122A (en) * | 2017-08-03 | 2019-02-06 | Rolls Royce Plc | Gas turbine engine |
| FR3102694B1 (en) | 2019-10-30 | 2022-06-03 | Safran Aircraft Engines | PROCESS FOR COMPACTING AN ANTI-CORROSION COATING |
| CN111673622A (en) * | 2020-06-01 | 2020-09-18 | 江苏佰健环保科技有限公司 | Environment-friendly cleaning process and equipment for food utensil non-stick coating |
| CN113996602A (en) * | 2021-11-02 | 2022-02-01 | 东南大学 | A kind of hole drilling and dirt cleaning method of printed circuit board |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA532346A (en) * | 1956-10-30 | D. Smith Rowland | Method of cleaning glass-working tools | |
| US2710286A (en) * | 1953-02-25 | 1955-06-07 | Rca Corp | Method of removing and salvaging adherent materials |
| US3963627A (en) * | 1970-02-16 | 1976-06-15 | Imperial Chemical Industries Limited | Surface treatment of particulate solids |
| US4020857A (en) * | 1976-04-13 | 1977-05-03 | Louis Frank Rendemonti | Apparatus and method for pressure cleaning and waxing automobiles and the like |
| GB1603085A (en) * | 1977-06-03 | 1981-11-18 | Ciba Geigy Uk Ltd | Fire protection means |
| US4174531A (en) * | 1977-11-14 | 1979-11-13 | Rca Corporation | Printed circuit board with increased arc track resistance |
| US4174571A (en) * | 1978-07-28 | 1979-11-20 | Dentron, Inc. | Method for cleaning teeth |
| US4412402A (en) * | 1978-07-28 | 1983-11-01 | Cavitron Inc. | Equipment and method for delivering an abrasive-laden gas stream |
| SE455265B (en) * | 1984-03-27 | 1988-07-04 | Arne Alvemarker | BLASTER BODIES OF COMPOSITION MATERIAL TO CLEAN CLEANING DISH |
| US4588444A (en) * | 1984-04-04 | 1986-05-13 | Anderson Ronald L | Method for cleaning polymeric contact lenses |
| US4731125A (en) * | 1984-04-19 | 1988-03-15 | Carr Lawrence S | Media blast paint removal system |
| IL93572A (en) * | 1989-03-14 | 1993-06-10 | Church & Dwight Co Inc | Process for removing coatings from sensitive substrates and blasting media useful therein |
-
1991
- 1991-03-26 NZ NZ237596A patent/NZ237596A/en unknown
- 1991-03-30 MY MYPI91000529A patent/MY109653A/en unknown
- 1991-04-04 KR KR1019920702462A patent/KR960003113B1/en not_active Expired - Fee Related
- 1991-04-04 JP JP3510591A patent/JPH0669668B2/en not_active Expired - Fee Related
- 1991-04-04 EP EP19910911117 patent/EP0525122A4/en not_active Ceased
- 1991-04-04 CA CA002079892A patent/CA2079892C/en not_active Expired - Lifetime
- 1991-04-04 WO PCT/US1991/002338 patent/WO1991015308A1/en not_active Ceased
- 1991-04-04 AU AU79828/91A patent/AU643039B2/en not_active Ceased
- 1991-04-05 PL PL91289763A patent/PL165174B1/en unknown
- 1991-04-05 TR TR91/0360A patent/TR25589A/en unknown
- 1991-04-06 CN CN91103072.7A patent/CN1029599C/en not_active Expired - Fee Related
-
1992
- 1992-10-01 NO NO923823A patent/NO176751C/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0525122A1 (en) | 1993-02-03 |
| CA2079892C (en) | 1996-01-23 |
| TR25589A (en) | 1993-07-01 |
| PL165174B1 (en) | 1994-11-30 |
| AU643039B2 (en) | 1993-11-04 |
| MY109653A (en) | 1997-03-31 |
| JPH05504919A (en) | 1993-07-29 |
| KR960003113B1 (en) | 1996-03-05 |
| NZ237596A (en) | 1993-03-26 |
| WO1991015308A1 (en) | 1991-10-17 |
| CN1056077A (en) | 1991-11-13 |
| NO923823L (en) | 1992-11-30 |
| EP0525122A4 (en) | 1993-04-28 |
| CA2079892A1 (en) | 1991-10-07 |
| NO923823D0 (en) | 1992-10-01 |
| CN1029599C (en) | 1995-08-30 |
| AU7982891A (en) | 1991-10-30 |
| NO176751C (en) | 1995-05-24 |
| NO176751B (en) | 1995-02-13 |
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| LAPS | Cancellation because of no payment of annual fees |