AU568962B2 - Method for making artificial snow - Google Patents
Method for making artificial snowInfo
- Publication number
- AU568962B2 AU568962B2 AU50148/85A AU5014885A AU568962B2 AU 568962 B2 AU568962 B2 AU 568962B2 AU 50148/85 A AU50148/85 A AU 50148/85A AU 5014885 A AU5014885 A AU 5014885A AU 568962 B2 AU568962 B2 AU 568962B2
- Authority
- AU
- Australia
- Prior art keywords
- water
- snow
- swellable material
- water swellable
- crystals
- 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.)
- Ceased
Links
- 238000000034 method Methods 0.000 title claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 62
- 229920000642 polymer Polymers 0.000 claims description 34
- 239000013078 crystal Substances 0.000 claims description 31
- 239000000463 material Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 238000007710 freezing Methods 0.000 claims description 4
- 230000008014 freezing Effects 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- -1 aromatic alcohols Chemical class 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 239000003093 cationic surfactant Substances 0.000 claims description 3
- 238000004132 cross linking Methods 0.000 claims description 3
- 239000003599 detergent Substances 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical class COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
- 238000013019 agitation Methods 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 229920000058 polyacrylate Chemical class 0.000 claims description 2
- 239000000344 soap Substances 0.000 claims description 2
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 claims description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 2
- 230000008961 swelling Effects 0.000 claims description 2
- 229920001897 terpolymer Polymers 0.000 claims description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical class COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 238000005057 refrigeration Methods 0.000 description 11
- 239000003570 air Substances 0.000 description 10
- 239000012080 ambient air Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 4
- 241000533950 Leucojum Species 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000003507 refrigerant Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229920006037 cross link polymer Polymers 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical class OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- 239000004160 Ammonium persulphate Substances 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- 235000019395 ammonium persulphate Nutrition 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000005413 snowmelt Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
Landscapes
- Buildings Adapted To Withstand Abnormal External Influences (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Description
Title: "METHOD FOR MAKING ARTIFICIAL SNOW" BACKGROUND OF THE INVENTION
(1 ) Field of the Invention
This invention relates to a method for making artificial snow, and to a skiing slope using such snow.
(2) Description of the Prior Art
In certain ski resorts around the world, artific¬ ial skiing slopes are produced by a number of different techniques. One method is to create artificial snow by' using machines which spray atomised water and compressed air (or other gas) into a subzero atmosphere to create a blanket of snow. The adiabatic expansion of the air absorbs heat from the atomised water and the particles freeze to form snow flakes. The machines are expensive to instal and operate, requiring large volumes of com¬ pressed air and are only capable of producing skiable snow when both the air and ground temperatures are below Θ°C to prevent the snow from melting. In spite of the large capital and operating costs, such machines are currently in use as they can extend the skiing season by upto one month in certain resorts.
The basic method for producing snow using this type of technique was disclosed in U.S. Patent No, 2,676, 471 (Pierce). Improved methods and apparatus for this technique are disclosed in U.S. Nos. 3,716,190 (Lindlof); 3,010,660 (Barnett); 3,301,485 (Tropeano); 3,298,612 (Torrens); 3,761,020 (Tropeano et al); 3,774,843 (Rice); 3,774,842 (Howell); 3,945,567 (Rambach); 4,004,732 (Hanson); 4,083,492 (Dewey); 4,105,161 (Kircher et al); and 3,733,029 (Eustis et al) and Australian Patent Application Nos. 77956/75 (Burns) and 12534/83 (Albert- son) .
The atomised water particles can be fed into an airflow generated by a fan (e.g. as shown in U.S. Patent
Nos. 3,760,598 (Jakob et al) and 2,968,164 (Hanson) and the formation of the snow flakes or crystals can be accelerated by seeding with nucleating agents such as ice crystals (see U.S. Patent No. 3,596,476 (Jakob et al) and bacteria (see U.S. Patent No. 4,200,228 (Woerpel) .
To prevent the artificial snow from melting, U.S. Patent No. 3,893,507 (MacCracken et al) and Austrian Patent No. 363962 (Michaelis) disclose methods of freezing or cooling the ground using refrigeration systems of the type used for skating rinks and in mining. These methods do not overcome the problem of the snowflakes melting in the air and the constant refrigeration of the snow formed e.g. by the Pierce method, will eventually turn to a glaze of ice, unsuitable for skiing, as heat from the air above the snow is absorbed via the snow to the refrigeration.
In more temperate zones, artificial skiing slopes have been developed using mats, bristles or carpets of synthetic materials. Such slopes are sold under the Trade Marks "Dendex", "Delta", and "Dri-Sno" and form the subject of U.S. Patent Nos. 3,400,643 (Holley) and 3,731,923 (Grieve) and Australian Patent Application No. 71499/74 (Snow Products Inc). These slopes require the use of special skis and poles and cannot truly recreate a snow-covered slope.
SUMMARY OF THE PRESENT INVENTION It is an object of the present invention to provide a method for making artificial snow which is relatively simple and inexpensive.
It is a preferred object to provide a method which enables the snow to be used and maintained at temperatures not previously considered possible.
It is a further preferred object to provide a method where the snow can be laid in layers e.g. of different
crystal size to recreate "powder" snow and hard- packed snow.
It is a still further preferred object to provide a method where the snow can be recovered and reused, or retreated, as required.
It is a still further preferred object to produce a ski slope incorporating the snow produced by the present method.
Other preferred objects will become apparent from the following description.
In one aspect the present invention resides in a method of making artificial snow including the steps of:
(a) mixing water with a water swellable material at less than the maximum water retention capacity of the material;
(b) aerating the mixture; and
(c) freezing the mixture to form snow crystals. Preferably the water swellable materials include all polymers, copolymers and terpolymers capable of swelling in an aqueous solution with a high gel strength. These include the polymers and copolymers of acrylamide, acrylic acid, polyacrylate salts, vinyloxazolidinane, methacrylate salts, styrene, vinyl ether and salts of styrene sulphonates, together with polymers and copolym- ers polymerized with cellulosic fibres. Suitable polymers are described in U.S. Patent Nos. 3,247,171 (Walker et al); 3,022,279 (Proffitt); 3,022,280 (Shukys); and 3,251,194; British Patent Application 2,127005 (Chemical Discoveries SA) and Australian Patent No. 464077 (The Dow Chemical Company) .
It is more preferred that the polymer will absorb approximately 30-100 times its own weight in water to provide good gel strength, minimum evaporation and decreased permeability. Preferably, for hard snow the water swellable
polymer is mixed with the water at 30-85%, more preferably 50-70%, of its maximum water retention capacity. This may be at e.g. a nature of 50 parts water: 1 part polymer (by weight). Preferably for fine powder snow the polymer is mixed with the water at 5-50% more preferably 5-15% of its maximum water retention capacity. Such mixture may include 5-15 parts water: 1 part polymer (by weight).
A surfactant may be added to the mixture to reduce the surface tension of the water and to produce minute bubbles within the matrix of the snow crystals to create a honeycomb effect. Suitable surfactants include soap and detergents; sulphated, aliphatic or aromatic alcohols; linear or branched chain alkylbsn- zene sulphonates; alkylarine sulphonates; sodium dodecyl- benzene sulphonate; alkyl sulphonates; and anionic, cationic and non-ionic surfactants. When anionic or cationic surfactants are used, the polymer becomes anionic or cationic and causes the snow crystals to oppose each other.
The mixture may be aerated by spraying_ through a nozzle or by mechanical agitation or whipping in a - mixing chamber.
The mixture may be frozen at 0 C or below, the hardness of the ice being increased with decreasing temperature as additional water within each crystal is caused to freeze. (It has been observed that the snow crystals are formed when approximately 5% of the water contained within the polymer turns to ice. A practical minimum temperature is approximately -20 C.
The snow is preferably laid on a refrigerated floor to a depth of 75-200mm, more preferably 125-150mm to form a skiing slope. Preferably the snow is laid in layers in a manner similar to natural snow. The refrig- erated floor may be of the type used for ice skating rink
floors and suitable examples are described in Austrian Patent No. 363962 (Michaelis); U.S. Patent Nos. 3,893,507; 3,379,031; 2,878,651 and 3,751,935 or the "Holmsten Rink- master" sold by Holmsten Ice Rinks Inc. of St. Paul, Minnesota, U.S.A. TO control any likelihood of environ¬ mental damage should the snow melt, the floor is prefer¬ ably surrounded by side walls.
The refrigeration tonnage to maintain the snow frozen will be dependent on ambient air temperatures. The top layer of the snow crystals may be shaved or removed from the slope, the crystals melted back to the gel and any foreign matter filtered out before refreezing and relaying on the slope.
In a second aspect the present invention resides in a skiing slope incorporating the artificial snow made by the above method.
BRIEF DESCRIPTION OF THE DRAWINGS To enable the invention to be fully understood, a preferred embodiment will now be described with reference to the accompanying drawings, in which:
FIG. 1 is a part-sectional, part-schematic view of the skiing slope; and
FIG. 2 is a schematic layout of the alternative snow-crystal manufacturing equipment. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The water swellable polymer to be mixed with the water and frozen to produce the snow crystals may be formed from the following ingredients, by way of an example: 100ml water 20 ml Acrylamide Monomer
1 ml Tetramethylethylenediamine 4 ml 7% Ammonium Persulphate
0-4 gm Methylene Bisachylamide (0.002 - 0.005%) 10-50 ml detergent surfactant (optional) The ingredients are mixed well and allowed to react
exothermically to produce a highly cross-linked polymer matrix capable of retaining 50-100 times its own weight of water. The resultant gel is dried and ground into a powder or cast into flakes or granules. The production of a skiing slope using the poly¬ acrylamide powder will now be described with reference to FIG. 1.
The skiing slope 10 is laid out on the side of a mountain or hill to provide a downhill run. The slope is delineated by side walls 11 which controls any run-off of the water/polymer mixture should the snow crystals melt. This avoids the likelihood of any damage to the surrounding environment.
Flexible refrigeration pipes 12 are laid in a sand bed 13 on a subsoil base 14. The refrigerant pipes are connected to respective manifolds 15, which are connected to a refrigeration unit 16. Refrigerant e.g. brine from the pipes 12 is passed through a heat exchanger 17 and returned via a brine pump 18. The heat from the refrig- erant is dissipated by liquid circulated through the heat exchanger 17 and a cooling tower 19 by a pump 20.
Water, from a supply tank 21, and the polyacryla¬ mide powder, from a supply hopper 22, are fed into a mixing chamber 23 at the rate of 50 parts water: 1 part polymer by weight and are mixed so that the polymer absorbs the water to approximately 50% of its maximum water retention capacity.
The resultant gel is pumped through a line 24 into which is injected air by an air compressor 25. From the air compressor, the aerated gel is carried through lines 26 into manifolds 27 fitted with a series of spaced nozzles which spray the aerated gel over the refrigerated floor 28 created by the refrigeration pipes 12 and sand bed 13. As the air above the floor is below 0°C, the water
in the polymer particles sprayed from the nozzles begins to freeze and the snow crystals are formed as soon as 5% of the water becomes frozen, this water forming a frozen shell around the balance of the water absorbed in the polymer particles. Because the polymer is highly cross-linked, the pores in the polymer part¬ icles are very small and so little cross-linking between the crystals, due to the presence of the ice in the crystal. occurs. The layers of snow crystals are laid approximately 25mm thick at a time until the snow is approximately 125-150 mm thick. All the snow in these layers have the nature of natural hard packed snow.
A thin layer e.g. 6-12 mm thick of fine powder snow is then formed on top of the snow already laid. The water • polymer ratio is reduced to 5-15 parts water: 1 part poly¬ mer. Because of the higher polymer content, the snow acts as an insulator against absorbing heat from the ambient air and the CQ-NH side chains absorbs UV radiation If rain should fall , the polymer can absorb some of the water without damaging the skiing surface.
Tests have shown that by reducing the temperatures e.g. to -20°C, the percentage of water absorbed in the polymer which freezes increases e.g. to 85% and if the temperature is allowed to increase e.g. to -2°C, the ice within the frozen ice shell will melt without causing the snow crystals to break down and reform the gel. However, as the temperature is reduced, the crystals become harder due to the higher ice content.
This phenomenon leads to significant savings in the operating costs for the refrigeration unit 16. At night, when the ambient air temperature is low, the refrigeration unit can be operated to lower the snow crystal temperature to e.g. -18 C. During the day, the higher ambient air temperature heats up the crystals but provided the snow temperature does not exceed e.g. -1.8°C,
the snow is unaffected. Even if the ambient temperature becomes relatively high e.g. 5-10 C, the refrigeration unit need only be operated from a short period to maintain the snow temperature below the critical temperature of e.g. -1.8 C. (The critical temperature will be dependant in part on the particular polymer used).
An insulated cover e.g. of plastics material may be supported over the slope to act as a weatherproof barrier to protect the skiers (and reduce the absorption of heat by the snow from the ambient air).
To maintain the skiing surface, a thin layer can be shaved off and placed in side drains 29 along the sides of the slope 10. The snow melts and is drawn off via pipes 30 to a filter unit 31 where any foreign matter e.g. dirt is removed. (Because the highly cross-linked polymer particles have a small pore size, little foreign matter will enter the particles). The now cleaned gel is returned to the mixing chamber 23 for return to the slope where it can be sprayed onto the existing snow in the fine powder snow layer. (It may be necessary to maintain the necessary water/polymer ratio).
By laying the refrigeration pipes 12 out in sections down the slope, the length and width of the slope can be varied throughout the year. For example, in mid-summer, the slope may be 100 metres long. As summer turns to autumn, and the ambient air temperature drops, additional sections of the slope can be provided with the artificial snow until in mid-winter, the slope may be e.g. 400-500 metres long. As spring brings warmer ambient temperatures, and natural snowfalls decrease, additional artificial snow is produced to maintain the slope at maximum length and the normal skiing season may be extended by e.g. 30 days. Then as spring turns to summer, sections of the slope may be closed. To save costs, the melted snow can be drained off
and filtered and the gel stored for next season. (If preferred, the polymer may be dried and stored in powder form) .
In a modified form of the invention (see FIG. 2), the water and polymer are mixed in the mixing chamber 23 as hereinbefore described but the aerated gel is instantly frozen in a freezing unit 3 using liquid nitrogen. The resultant snow crystals can then be spread over the slope 10 and built up in layers to the desired depth.
It will be readily apparent to the skilled addressee that the embodiments described are by way of illustrative examples only. In particular, by varying the ratio of water to polymer in the described ranges, and the temperature at which the snow is frozen the characteristics of the snow crystals can be varied. The characteristics will also be dependant on the degree of cross-linking of the polymer and the crystal size and the particular polymer used. Various changes and modifications can be made to the embodiments described without departing from the scope of the appended claims.
Claims (18)
1. A method for making artificial snow including the steps of:
(a) mixing water with a water swellable material at less than the maximum water retention capacity of the material;
(b) aerating the mixture; and
(c) freezing the mixture to form snow crystals.
2. A method as claimed in Claim 1 wherein: the water swellable material is a polymer, copolymer or terpolymers capable of swelling in an aqueous solution with a high gel strength.
3. A method as claimed in Claim 2 wherein: the water swellable material will absorb approx¬ imately 30-100 times its own weight in water.
4. A method as claimed in Claim 2 wherein: the water swellable material includes the polymers and copolymers of acrylamide; acrylic acid; polyacrylate salts; vinyloxazolidinane; methylacrylate salts; styrene; vinyl ether and salts of styrene sulph¬ onates.
5. A method as claimed in Claim 4 wherein the polymers and copolymers are polymerized with cellulosic fibres.
6. A method as claimed in Claim 1 wherein: for hard snow, the water swellable material is mixed with the water at 30-85% of its maximum water retent¬ ion capacity.
7. A method as claimed in Claim 6 wherein: the water swellable material is mixed at 50-70% of its maximum water retention capacity.
8. A method as claimed in Claim 1 wherein: for fine powder snow, the water swellable material is mixed with the water at 5-50% of its maximum water retention capacity.
9. A method as claimed in Claim 8 wherein: the water swellable material is mixed with the water at 5-15% of its maximum water retention capacity.
10. A method as claimed in Claim 2 wherein: the water swellable material will absorb 100 times its own weight in water; and for hard snow the water and water swellable material are mixed in the ratio 50 parts water: 1 part water swellable material by weight.
11. A method as claimed in Claim 2 wherein: the water swellable material will absorb 100 times its own weight of water; and for fine powder snow, the water and the water swellable material are mixed in the ratio of 5-15 parts water: 1 part water swellable material by weight.
12. A method as claimed in Claim 1 wherein: the mixture is aerated by mechanical agitation or compressed air or gas.
13. A method as claimed in Claim 1 wherein: the mixture is frozen in the temperature range of -20°C to 0°C.
14. A method as claimed in Claim 4 or Claim 5 wherein: the snow crystals are formed when at least 5% of the water absorbed in the polymer, copolymer and ter- polymer is converted to ice, little crosslinking occurring between the respective crystals.
15. A method as claimed in Claim 1 wherein: a surfactant is added to the mixture to reduce the surface tension of the water and produce minute bubbles which create a honeycomb effect within the snow crystals.
16. A method as claimed in Claim 15 wherein the surf¬ actant includes : soap; detergents; sulphated, aliphatic or aromatic alcohols; linear or branched chain alkylbenzene sulphonates; alkylarine sulphonates; sodium dodecylbenzene sulphonate; alkyl sulphonates; and anionic, cationic and non-ionic surfactants.
17. A method as claimed in Claim 1 wherein: the snow crystals are sprayed or laid on a refrigerated floor in layers to a depth of 75-200 mm.
18. A skiing slope including: a refrigerated floor; and one or more layers of snow crystals covering the floor, the snow crystals being made by the method of any one of Claims 1 to 17.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU50148/85A AU568962B2 (en) | 1984-11-06 | 1985-11-04 | Method for making artificial snow |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPG800384 | 1984-11-06 | ||
| AUPG8003 | 1984-11-06 | ||
| AUPH0057 | 1985-04-09 | ||
| AU50148/85A AU568962B2 (en) | 1984-11-06 | 1985-11-04 | Method for making artificial snow |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU5014885A AU5014885A (en) | 1986-06-03 |
| AU568962B2 true AU568962B2 (en) | 1988-01-14 |
Family
ID=25628783
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU50148/85A Ceased AU568962B2 (en) | 1984-11-06 | 1985-11-04 | Method for making artificial snow |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU568962B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU622354B1 (en) * | 1990-10-15 | 1992-04-02 | Kun-Nan Lo | Connector for chain stay and seat stay |
| AU648286B2 (en) * | 1990-02-02 | 1994-04-21 | Snova Corporation | Artificial snow granule, snow quality improver and method for making the same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07110937B2 (en) * | 1987-10-22 | 1995-11-29 | パーマスノー(オーストラレーシア)リミテッド | Manufacturing method of artificial snow |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3251194A (en) * | 1964-04-03 | 1966-05-17 | Dow Chemical Co | Method of making an ice skating rink |
| US3257815A (en) * | 1964-07-10 | 1966-06-28 | Conch Int Methane Ltd | Method and apparatus for the largescale production of snow fields for sports use |
-
1985
- 1985-11-04 AU AU50148/85A patent/AU568962B2/en not_active Ceased
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3251194A (en) * | 1964-04-03 | 1966-05-17 | Dow Chemical Co | Method of making an ice skating rink |
| US3257815A (en) * | 1964-07-10 | 1966-06-28 | Conch Int Methane Ltd | Method and apparatus for the largescale production of snow fields for sports use |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU648286B2 (en) * | 1990-02-02 | 1994-04-21 | Snova Corporation | Artificial snow granule, snow quality improver and method for making the same |
| AU622354B1 (en) * | 1990-10-15 | 1992-04-02 | Kun-Nan Lo | Connector for chain stay and seat stay |
Also Published As
| Publication number | Publication date |
|---|---|
| AU5014885A (en) | 1986-06-03 |
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