GB2119298A - Method of abrading surfaces - Google Patents
Method of abrading surfaces Download PDFInfo
- Publication number
- GB2119298A GB2119298A GB08312002A GB8312002A GB2119298A GB 2119298 A GB2119298 A GB 2119298A GB 08312002 A GB08312002 A GB 08312002A GB 8312002 A GB8312002 A GB 8312002A GB 2119298 A GB2119298 A GB 2119298A
- Authority
- GB
- United Kingdom
- Prior art keywords
- urea
- abrasive
- blasting
- process according
- particles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 15
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000004202 carbamide Substances 0.000 claims abstract description 31
- 238000005270 abrasive blasting Methods 0.000 claims abstract description 6
- 239000002245 particle Substances 0.000 claims description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 238000005422 blasting Methods 0.000 claims description 15
- 239000003973 paint Substances 0.000 claims description 14
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 239000007921 spray Substances 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 6
- 235000000346 sugar Nutrition 0.000 description 6
- 239000000428 dust Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000005299 abrasion Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000002195 soluble material Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 238000000429 assembly Methods 0.000 description 2
- 230000000712 assembly Effects 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- MIMUSZHMZBJBPO-UHFFFAOYSA-N 6-methoxy-8-nitroquinoline Chemical compound N1=CC=CC2=CC(OC)=CC([N+]([O-])=O)=C21 MIMUSZHMZBJBPO-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229910000531 Co alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 229910001069 Ti alloy Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 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
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
- B24C1/00—Methods for use of abrasive blasting for producing particular effects; Use of auxiliary equipment in connection with such methods
- B24C1/003—Methods for use of abrasive blasting for producing particular effects; Use of auxiliary equipment in connection with such methods using material which dissolves or changes phase after the treatment, e.g. ice, CO2
-
- 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
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Particulate urea is used as the abrasive in dry abrasive blasting processes.
Description
SPECIFICATION
Method of abrading surfaces
It is well known to abrade surfaces by dry abrasive blasting methods. Such methods comprise blasting abrasive particles against a surface by directing onto the surface a stream of the abrasive particles entrained in a large volume of gas. Typical abrasive particles that are used include alumina, sand, crushed shells, silicon carbide, powdered glass and metal particles.
If the surfaces are of complex shape there may be a tendency for abrasive particles to be entrapped by the surfaces and to remain on them after the abrasion is completed. This is very undesirable, especially when the surfaces are to serve as components in assemblies that involve moving parts.
During use the particles may become dislodged from the surfaces where they are entrapped and cause severe wear. Examples of such surfaces are pistons, crankshafts and bearings in motor assemblies and hollow blades and other components of jet engines.
It might be thought possible to minimise this problem by using water soluble abrasive particles and water washing the surfaces after the blasting.
Unfortunately none of the water washable particles that have been proposed previously have proved to be satisfactory in practice.
In the invention the abrasive particles are urea particles. If desired the surface that has been blasted with them may be washed with water to remove any that have been entrapped by the surface.
The urea particles generally have a size of at least 0.01 mm since although smaller particles can be used as abrasive there is generally no advantage in using them and there can be the disadvantage of undesirable dusting problems. Normally the particle size is at least 0.05 mm and most preferably at least 0.1 mm. The particles are not usually larger than about 2 or 3 mm in particle size since particles as large as this or larger than this tend to give rather coarse abrasion. However for some purposes this may be desired. Generally the particle size is not more than about 1 mm with values of around 0.1 to 0.6 mm generally being particularly suitable. The particles may be commercial grade crystalline urea but preferably are urea prills.Many commercial grades of urea prills can have a particle size larger than is desired in the invention and so the preferred products are those known as urea microprills, for instance the product supplied by Chemie Linz AG under the name "Biuron" microprilled urea.
The urea particles are preferably used as the sole abrasive in the dry blasting method. They may be directed onto the surface in conventional manner.
Thus they are made to impinge at high velocity onto the surface by entrainment in a high velocity stream of a large volume of air or other inert gas. This stream may be generated by forcing compressed air out of a nozzle. The particles are entrained in the stream, generally before ejection from the nozzle, by conventional means such as a suitably designed hopper or by venturi action. Typically the air pressure is at least 1 kg/cm2 but is generally not more than about 8 kg/cm2. Air pressures of between 2.5 and 6 kg/cm2 are often preferred. The volume of air (measured at standard pressure) is generally very large compared to the volume of urea entrained in it, typically being more than 1,000 times the volume of urea.
The dry blasting is preferably conducted while the surfaces are enclosed within a dry blasting cabinet, but this is not essential. Generally the particles that have been blasted onto the surfaces are collected and reused until they become too contaminated.
After the dry blasting operation has been completed the surfaces may be washed with water, typically at ambient temperatures, for instance by immersion or, more usually, by application of spray or jets of water.
The use of urea results in satisfactory abrasion and avoids the disadvantages of using water insoluble particles or other water soluble particles. Typical water soluble particles that might be considered as alternatives for urea include salt, sugars, sodium benzoate, citric acid and certain other crystalline acids, and salts of various organic and inorganic acids, for instance ammonium bifluoride. However all these other materials have serious disadvantages that are not possessed by urea.
Many of the materials are highly acidic or highly alkaline when dissolved in water and therefore tend to cause corrosion of the surfaces and/or effluent discharge problems. An example is citric acid. Many of the materials accelerate corrosion of metal surfaces even though they may not be acidic or alkaline when dissolved in water. For instance metal surfaces of aluminium, magnesium, steel, titanium, nickel and cobalt based alloys may tend to be corroded when sodium chloride is used as the abrasive and is subsequently washed. Further it is well known that the specialised metals and metal alloys that are often used in components of, for instance, turbine engines and other devices should not be brought into contact with certain elements which many water soluble materials do contain.Thus compounds containing elements such as sulphur, chlorine, fluorine, bromine, iodine, sodium, lead, antimony, bismuth and zinc should not be brought into contact with such components. These criteria alone render unsuitable many water soluble abrasive particulate materials.
Another problem that arises with many water soluble materials is the risk of explosion. Materials such as sugar can result in the formation of inflammable residues or explosive dust clouds during dry blasting where oxygen from the compressed air stream or from the surroundings may admix with finely dispersed powder particles.
Another problem arises from effluent disposal in that many water soluble materials create a solution that is toxic by ingestion and/or is harmful to the environment. Examples are sodium hydroxide, sodium cyanide and oxalic acid.
Finally, many water soluble materials which in theory might be suitable in practice are not commercially available in a particulate form having the desired particle size or powder rheology. Examples include some grades of sugar and sodium laurate.
Urea avoids all these disadvantages, is very water soluble, and is readily available in suitable, free flowing, particulate form. It is non combustible. The commerically available grades of urea generally contain negligible quantities of harmful materials.
Aqueous solutions of urea are only mildly alkaline and so are relatively non-corrosive to sensitive metals. Its existing agricultural and industrial uses have established that it is basically not harmful to the environment. It occurs naturally in the blood stream in measurable concentrations and there is no evidence that it presents any health hazard.
Bythe invention it is therefore possible to abrade simple or complex metallic, or sometimes nonmetallic, surfaces and effectively remove mill scale, corrosion products, unwanted paint and many other kinds of surface contamination. In addition to or instead of this abrasion the blasting with urea can impart a certain roughness to the surface and this may be desirable as a pre-treatment for subsequent surface treatments, for instance to assist adhesion of a subsequentiy applied coating obtained by painting or plating.
The invention is of particular value for the removal of paint, especially after treatment of the paint with a suitable paint remover. For instance a surface carrying a paint coating, or residues of a paint coating, may be immersed or otherwise treated with a paint remover and the partially degraded paint may then be removed by blasting with urea.
The following are examples of the invention, example 1 being comparative.
Example 1 An experiment was carried out using a portable dry blasting cleaning rig of the type marketed by
Hodge-Clemco Ltd. In this experiment sugar granules were used as the dry abrasive blast medium and they were fed into a compressed air stream via a powder hopper and ejected with the compressed air at a 6.2 mm nozzle. The air pressure was 40 psi (2.8 kg/cm2).
The jet of particles was made to impinge on a titanium compressor blade from a commercial jet engine, the blade having been previously soiled by running in the engine and covered with a layer of carbonaceous 'sooty' deposits requiring removal before reassembly of the engine and for inspection purposes.
The attempt resulted in a poor cleaning performance in which sugar granules which had broken down on impact adhered to the surface to be cleaned and built-up on that surface preventing any further abrasive cleaning effect on the underlying carbonaceous contamination.
Large volumes of sugar dust were generated in the cleaning attempt and a hazard of combustion and possibly explosion of the dust cloud was present.
Example 2
In this example a further dirty section of the same compressor blade was abraded in a similar cleaning rig but using a different air nozzle and a different abrasive. The air pressure was 80 psi (5.6 kg/cm2) and the ejector nozzle orifice was 3.2 mm. The abrasive particles were of crystalline urea, and in particular the microprilled urea sold under the trade name "Biuron", typically having a particle size of around 0.5 mm.
Blasting was conducted for about 45 seconds, during which about 0.5 kg urea was blasted onto the surface.
A good abrasive cleaning effect was observed with no significant build-up of urea particles on the surface. Small deposits of dust that did remain were easily washed away with cold water. Although clouds of dust were formed they created no fire or other hazard and no ill effects to the operators were noted.
Example 3
In this example a chromated magnesium bearing carrier coated with Rockhard (an epoxy resin) and a green epoxy top coat was immersed in a solvent type paint remover operated at 100"C for a period of 3 hours. The softened paint was then removed by blasting with urea. The pressure was 80 psi (5.6 kg/cm2) with a nozzle orifice of 4 mm. Finally the surface was water rinsed to dissolve and hence remove final traces of the blasting medium. On areas not blasted with urea but only rinsed with water, removal of the paint scheme was incomplete.
Claims (10)
1. A process in which a surface is cleaned by dry abrasive blasting using particulate urea as the abrasive.
2. A process according to claim 1 in which the particulate urea has a particle size of 0.1 to 1 mm.
3. A process according to claim 2 in which the particulate urea is in the form of micropriils.
4. A process according to any preceding claim in which, after the dry blasting, the surface is washed with water to remove residual urea.
5. A process according to claim 4 in which the washing is effected by application of water to the surface by sprays or jets.
6. A process according to any preceding claim in which the dry abrasive blasting is conducted in a dry blasting cabinet.
7. A process according to any preceding claim in which the surface carries a paint coating or paint residues.
8. A process according to claim 7 in which the surface is treated with a paint remover before the abrasive blasting with urea.
9. A process according to claim 1 substantially as herein described with reference to examples 2 or 3.
10. An abrasive for dry abrasive blasting and that is particulate urea.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB08312002A GB2119298B (en) | 1982-05-04 | 1983-05-03 | Method of abrading surfaces |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8212866 | 1982-05-04 | ||
| GB08312002A GB2119298B (en) | 1982-05-04 | 1983-05-03 | Method of abrading surfaces |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB8312002D0 GB8312002D0 (en) | 1983-06-08 |
| GB2119298A true GB2119298A (en) | 1983-11-16 |
| GB2119298B GB2119298B (en) | 1985-11-27 |
Family
ID=26282727
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB08312002A Expired GB2119298B (en) | 1982-05-04 | 1983-05-03 | Method of abrading surfaces |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2119298B (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0178164A1 (en) * | 1984-10-10 | 1986-04-16 | Brent Chemicals International Plc | Method of cleaning surfaces |
| GR900100181A (en) * | 1989-03-14 | 1990-07-31 | Church & Dwight Co Inc | Process for removing coatings from sensitive substrates and blasting media useful therein |
| TR25648A (en) * | 1990-04-13 | 1993-07-01 | Church & Dwight Co Inc | PROCESS TO REMOVE COATINGS FROM PRECISE SUB-PLATES AND USEFUL SANDBLASTING ENVIRONMENT |
| ITGE20100010A1 (en) * | 2010-01-28 | 2011-07-29 | Alberto Rebaudi | "METHOD OF TREATMENT OF DENTAL AND ORTHOPEDIC SURFACES FOR ABLATION OBTAINED WITH HYDRO-SOLUBLE MATERIALS" |
| RU2707512C1 (en) * | 2019-07-11 | 2019-11-27 | Общество с ограниченной ответственностью "ЛУКОЙЛ-Нижегородниинефтепроект" | Apparatus for cleaning furnace and boilers heat exchange surfaces by blasting method |
| RU2714424C1 (en) * | 2019-07-17 | 2020-02-14 | Общество с ограниченной ответственностью "Сентро Восточная Европа" | Method of cleaning external surface of tubular coils inside heating equipment |
-
1983
- 1983-05-03 GB GB08312002A patent/GB2119298B/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0178164A1 (en) * | 1984-10-10 | 1986-04-16 | Brent Chemicals International Plc | Method of cleaning surfaces |
| GR900100181A (en) * | 1989-03-14 | 1990-07-31 | Church & Dwight Co Inc | Process for removing coatings from sensitive substrates and blasting media useful therein |
| TR25648A (en) * | 1990-04-13 | 1993-07-01 | Church & Dwight Co Inc | PROCESS TO REMOVE COATINGS FROM PRECISE SUB-PLATES AND USEFUL SANDBLASTING ENVIRONMENT |
| ITGE20100010A1 (en) * | 2010-01-28 | 2011-07-29 | Alberto Rebaudi | "METHOD OF TREATMENT OF DENTAL AND ORTHOPEDIC SURFACES FOR ABLATION OBTAINED WITH HYDRO-SOLUBLE MATERIALS" |
| RU2707512C1 (en) * | 2019-07-11 | 2019-11-27 | Общество с ограниченной ответственностью "ЛУКОЙЛ-Нижегородниинефтепроект" | Apparatus for cleaning furnace and boilers heat exchange surfaces by blasting method |
| RU2714424C1 (en) * | 2019-07-17 | 2020-02-14 | Общество с ограниченной ответственностью "Сентро Восточная Европа" | Method of cleaning external surface of tubular coils inside heating equipment |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2119298B (en) | 1985-11-27 |
| GB8312002D0 (en) | 1983-06-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |