US20090301105A1 - Method for the production of an ice surface for ice rinks - Google Patents

Method for the production of an ice surface for ice rinks Download PDF

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Publication number
US20090301105A1
US20090301105A1 US12/306,187 US30618707A US2009301105A1 US 20090301105 A1 US20090301105 A1 US 20090301105A1 US 30618707 A US30618707 A US 30618707A US 2009301105 A1 US2009301105 A1 US 2009301105A1
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US
United States
Prior art keywords
ice
water
added
substance
ppm
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.)
Abandoned
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US12/306,187
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English (en)
Inventor
Thomas Loerting
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Unversitat Innsbruck
Universitaet Innsbruck
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Unversitat Innsbruck
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Assigned to UNIVERSITAT INNSBRUCK reassignment UNIVERSITAT INNSBRUCK ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LOERTING, THOMAS
Publication of US20090301105A1 publication Critical patent/US20090301105A1/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/24Materials not provided for elsewhere for simulating ice or snow

Definitions

  • the invention starts out from a method for the production of an ice surface for an ice rink in accordance with the preamble of claim 1 .
  • the ice quality of an ice rink plays a central role particularly for speed competitions, e.g., speed skating.
  • the mechanical properties of the ice, correspondingly, of the ice surface of the ice rinks, can be controlled via various parameters, e.g. via the ice temperature, the relative atmospheric humidity or the conductivity of the water forming the ice.
  • a substance is admixed to the ice-forming water, said substance being ammonia, an alkali hydroxide or alkaline earth hydroxide, a hydrogen halide, nitric acid, sulfuric acid, phosphoric acid, an alkali salt, alkaline earth salt or ammonium salt of said acids, or ammonium-bicarbonate, or a mixture of several of said substances.
  • NH 3 , HF, HCl, HBr, HI, NH 4 I, NH 4 F, NH 4 Br, LiOH, NaOH, KOH, Ca(OH) 2 or a mixture of several of these substances are added to the water preferentially, since said substances, due to their physical-chemical properties, cause the strongest effect of all possible dopants.
  • the substance added to the water is added in a concentration of up to 5 ppm, which requires only small amounts of dopants and is thus cost-efficient.
  • the maximum concentration of the substance added to the water does not exceed 20 ppm, since thereby an environment-friendly and—with respect to contamination by possibly noxious substances—safe concentration is ensured.
  • the substance added to the water can be added by admixing to the water before freezing in the form of dilute solutions so that a homogeneous ice layer can be generated.
  • the substance added to the water can be added after freezing by treating the ice with a liquid which contains the additives because thereby also an ice surface which was prepared using un-doped water can be improved in terms of quality afterwards during post-processing of the ice surface, without the need of freezing a new ice surface from scratch.
  • the method according to the present invention thereby proposes for the production of ice by freezing of de-ionized water, to add admixtures purposefully to said water, i.e. to dope the water.
  • This brings about that properties such as the static as well as the dynamic coefficient of friction or the surface hardness can be selectively controlled by these additives.
  • the additive can either be added by admixing it to the water (before freezing) in the form of dilute solutions or by treating the ice (after freezing) with a liquid which contains the admixtures.
  • An adaption of currently used ice preparation machines is not necessary, since instead of water simply contaminated water, e.g., de-ionized water, tap water, distilled water, etc. can be used.
  • the doping of water with 4 ppm NH 3 is described here.
  • 10000 litres of water are needed. These are typically sprinkled onto a pre-cooled area using a hose, which is connected to the water pipe.
  • a uniform doping with NH 3 can e.g. be achieved by interconnecting a metering valve which doses a dilute NH 3 solution into the tap water in dependence on the rate of flow.
  • One e.g. provides one litre of a 4% solution of NH 3 , which is supposed to be dosed into the water.
  • the metering valve At a flow rate of 50 litres per minute the metering valve is supposed to dose in 5 millilitres per minute for a duration of 200 minutes. This results in a dilution of 1:10000 so that the tap water finally contains 4 ppm NH 3 .
  • the ice needs to be given the time to freeze homogeneously on the pre-cooled surface.
  • the protocols can be employed which are used by ice preparation specialists today. The more time the ice is given, i.e., the slower the cooling rates, the larger the crystals and the smoother the ice surface. If one cools faster, then smaller crystals result which abut upon each other and produce interfaces (“triple junctions” or “grain boundaries”, respectively)—the ice surface becomes rough.
  • the method is also suitable for a surface treatment of the ice using special ice preparation machines.
  • These machines which are for instance employed during the breaks in ice hockey matches, mostly have a water tank and a snow container. These machines collect abraded snow, fine down the topmost ice layer and apply a new layer of water onto the ice. If one mixes an appropriate amount of NH 3 also into the water tank of the machine, then previously un-doped ice benefits for the first time from the surface properties improved by the doping, or, correspondingly, in case of ice which has already been prepared by means of doping, the optimized properties of the doped ice persist even after repeated ice preparation.
  • 3 ppm HF bring about a considerable increase in the ice flow properties.
  • An ice-skater “cuts” into the ice with his blade and thereby displaces ice from the groove, which normally ends up as “snow” on the ice surface.
  • the displaced ice flows back into the (just produced) groove to a much greater extent so that firstly less “snow” comes to lie on the ice surface and secondly the degree of destruction of the ice surface is minimized.
  • the ice surface also becomes softer.
  • 3 ppm NH 3 instead, the opposite effect occurs, attrition is enforced, the ice surface gets destroyed more severely and also becomes harder.
  • NH 3 doped ice has a decisive advantage: Today, ice preparation specialists adjust the ice hardness via the temperature. Soft ice surfaces (e.g. for figure skaters) are produced by making “warm” ice (e.g., at ⁇ 3° C.), while hard ice surfaces require cooling to e.g. ⁇ 10° C., thereby consuming much energy. Using NH 3 doped ice one can produce harder ice already at higher temperatures in an energy-saving manner.
  • the method according to the invention is also suitable for controlling the coefficient of sliding friction. For instance it can be measured that a certain doping results in a water film even on an ice surface at ⁇ 80° C., which reduces dynamic friction. On un-doped ice this water film disappears already below approx. ⁇ 25° C. so that cryogenic ice is no longer slippery. It is also conceivable that a dopant is found which increases dynamic friction on ice strongly by suppressing the water film already at comparably high temperatures.
  • the investigated substances are built directly into the ice lattice up to concentrations of 5 ppm and change the microscopic properties such as relaxation times, H-transfer times, electric conductivity, etc. via the production of so-called D- or L-defects. This leads to a change of the macroscopic properties.
  • Other substances such as for example bigger inorganic molecules, organic molecules, etc. are not built into the crystal lattice, but merely into lattice voids or grain boundaries, in many cases they are even only discharged via the surface and, accordingly, do not alter the microscopic and macroscopic properties of ice.
  • the list of substances that are capable of being built into the crystal lattice and which are therefore suitable for doping comprises ammonia, alkali hydroxides and alkaline earth hydroxides, hydrogen halides, nitric acid, sulfuric acid, phosphoric acid, alkali salts, alkaline earth salts and ammonium salts of said acids, and ammonium-bicarbonate. Particularly preferred are thereby NH 3 (ammonia), HF, HCl, HBr, HI, NH 4 I, NH 4 F, NH 4 Br, LiOH, NaOH, KOH, Ca(OH) 2 or mixtures thereof, which have the highest potential and the maximum effect, respectively.
  • the range of concentrations which has to be covered results from the concentration of molecules directly (substitutionally) incorporated into the lattice plus from the minerals already present in the tap water.
  • the threshold for fluorides amounts to 1.5 ppm so that for a hard NH 3 -doped ice surface the softening effect of fluorides has to be compensated at first.
  • the maximum of 1.5 ppm for compensation plus 5 ppm which are substitutionally incorporated at the utmost result in a threshold of 6.5 ppm for doping the tap water. Including a safety margin, the maximum concentration which has an influence on the macroscopic ice properties is 20 ppm.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Management, Administration, Business Operations System, And Electronic Commerce (AREA)
US12/306,187 2006-06-23 2007-06-19 Method for the production of an ice surface for ice rinks Abandoned US20090301105A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AT0106706A AT503443B1 (de) 2006-06-23 2006-06-23 Verfahren zur herstellung einer eisfläche für eissportbahnen
ATA1067/2006 2006-06-23
PCT/AT2007/000298 WO2007147185A1 (fr) 2006-06-23 2007-06-19 Procédé pour produire une surface de glace pour des pistes de patinage

Publications (1)

Publication Number Publication Date
US20090301105A1 true US20090301105A1 (en) 2009-12-10

Family

ID=38458288

Family Applications (1)

Application Number Title Priority Date Filing Date
US12/306,187 Abandoned US20090301105A1 (en) 2006-06-23 2007-06-19 Method for the production of an ice surface for ice rinks

Country Status (6)

Country Link
US (1) US20090301105A1 (fr)
EP (1) EP2041234A1 (fr)
AT (1) AT503443B1 (fr)
CA (1) CA2655336A1 (fr)
RU (1) RU2009102028A (fr)
WO (1) WO2007147185A1 (fr)

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8664232B2 (en) 2002-08-21 2014-03-04 Boehringer Ingelheim Pharma Gmbh & Co. Kg 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US8673927B2 (en) 2006-05-04 2014-03-18 Boehringer Ingelheim International Gmbh Uses of DPP-IV inhibitors
US8846695B2 (en) 2009-01-07 2014-09-30 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients with inadequate glycemic control despite metformin therapy comprising a DPP-IV inhibitor
US8853156B2 (en) 2008-08-06 2014-10-07 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients inappropriate for metformin therapy
US8865729B2 (en) 2008-12-23 2014-10-21 Boehringer Ingelheim International Gmbh Salt forms of a xanthine compound
US8883805B2 (en) 2004-11-05 2014-11-11 Boehringer Ingelheim International Gmbh Process for the preparation of chiral 8-(3-aminopiperidin-1-yl)-xanthines
US8883800B2 (en) 2011-07-15 2014-11-11 Boehringer Ingelheim International Gmbh Substituted quinazolines, the preparation thereof and the use thereof in pharmaceutical compositions
US9034883B2 (en) 2010-11-15 2015-05-19 Boehringer Ingelheim International Gmbh Vasoprotective and cardioprotective antidiabetic therapy
US9149478B2 (en) 2010-06-24 2015-10-06 Boehringer Ingelheim International Gmbh Diabetes therapy
US9155705B2 (en) 2008-04-03 2015-10-13 Boehringer Ingelheim International Gmbh DPP-IV inhibitor combined with a further antidiabetic agent, tablets comprising such formulations, their use and process for their preparation
US9186392B2 (en) 2010-05-05 2015-11-17 Boehringer Ingelheim International Gmbh Combination therapy
US9266888B2 (en) 2006-05-04 2016-02-23 Boehringer Ingelheim International Gmbh Polymorphs
US9457029B2 (en) 2009-11-27 2016-10-04 Boehringer Ingelheim International Gmbh Treatment of genotyped diabetic patients with DPP-IV inhibitors such as linagliptin
US9486526B2 (en) 2008-08-06 2016-11-08 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients inappropriate for metformin therapy
US9526728B2 (en) 2014-02-28 2016-12-27 Boehringer Ingelheim International Gmbh Medical use of a DPP-4 inhibitor
US9526730B2 (en) 2012-05-14 2016-12-27 Boehringer Ingelheim International Gmbh Use of a DPP-4 inhibitor in podocytes related disorders and/or nephrotic syndrome
US9555001B2 (en) 2012-03-07 2017-01-31 Boehringer Ingelheim International Gmbh Pharmaceutical composition and uses thereof
US9713618B2 (en) 2012-05-24 2017-07-25 Boehringer Ingelheim International Gmbh Method for modifying food intake and regulating food preference with a DPP-4 inhibitor
US10155000B2 (en) 2016-06-10 2018-12-18 Boehringer Ingelheim International Gmbh Medical use of pharmaceutical combination or composition
US11033552B2 (en) 2006-05-04 2021-06-15 Boehringer Ingelheim International Gmbh DPP IV inhibitor formulations
AU2014280955B2 (en) * 2014-12-24 2021-07-22 Arctic Ice Project Generation and deployment of ice with modified optical and/or thermal properties
US20230075532A1 (en) * 2021-08-31 2023-03-09 Tsinghua University Ice rink and method for making ice surface of ice rink
US11911388B2 (en) 2008-10-16 2024-02-27 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral or non-oral antidiabetic drug

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO325902B1 (no) * 2006-12-12 2008-08-11 Icemining Technology As Fremgangsmate for oppstotting av gruverom, tunnel eller hulrom i jorden ved bruk av is med modifisert flytehastighet
CN113137794A (zh) * 2021-05-21 2021-07-20 松下冷机系统(大连)有限公司 一种速度滑冰场地的二氧化碳制冰管道系统

Citations (2)

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US3361213A (en) * 1965-09-13 1968-01-02 Mobil Oil Corp Method of decreasing friction loss in turbulent liquids
US4953360A (en) * 1989-09-27 1990-09-04 Slick Ice Limited Additive for treating water used to form ice

Family Cites Families (4)

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DE526224C (de) * 1927-01-26 1931-06-06 Edgar Vorwerk Verfahren zur Herstellung einer kuenstlichen Eisbahn
DE19940203A1 (de) * 1999-08-25 2001-03-08 Integral Energietechnik Gmbh Zusatzstoff für ein pumpfähiges Flüssigeisgemisch
CA2556394A1 (fr) * 2004-02-13 2005-08-25 Orca Bay Arena Limited Partnership Procede, appareil et composition permettant de fabriquer de la glace
RU2293934C2 (ru) * 2005-12-26 2007-02-20 Борис Алексеевич Кузнецов Способ получения двухслойного льда

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3361213A (en) * 1965-09-13 1968-01-02 Mobil Oil Corp Method of decreasing friction loss in turbulent liquids
US4953360A (en) * 1989-09-27 1990-09-04 Slick Ice Limited Additive for treating water used to form ice

Cited By (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9108964B2 (en) 2002-08-21 2015-08-18 Boehringer Ingelheim International Gmbh 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US9321791B2 (en) 2002-08-21 2016-04-26 Boehringer Ingelheim International Gmbh 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US10202383B2 (en) 2002-08-21 2019-02-12 Boehringer Ingelheim International Gmbh 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US10023574B2 (en) 2002-08-21 2018-07-17 Boehringer Ingelheim International Gmbh 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US9556175B2 (en) 2002-08-21 2017-01-31 Boehringer Ingelheim International Gmbh 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and thier use as pharmaceutical compositions
US8664232B2 (en) 2002-08-21 2014-03-04 Boehringer Ingelheim Pharma Gmbh & Co. Kg 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US8883805B2 (en) 2004-11-05 2014-11-11 Boehringer Ingelheim International Gmbh Process for the preparation of chiral 8-(3-aminopiperidin-1-yl)-xanthines
US9751855B2 (en) 2004-11-05 2017-09-05 Boehringer Ingelheim International Gmbh Process for the preparation of chiral 8-(3-aminopiperidin-1-yl)-xanthines
US9499546B2 (en) 2004-11-05 2016-11-22 Boehringer Ingelheim International Gmbh Process for the preparation of chiral 8-(3-aminopiperidin-1-yl)-xanthines
US11033552B2 (en) 2006-05-04 2021-06-15 Boehringer Ingelheim International Gmbh DPP IV inhibitor formulations
US11084819B2 (en) 2006-05-04 2021-08-10 Boehringer Ingelheim International Gmbh Polymorphs
US9493462B2 (en) 2006-05-04 2016-11-15 Boehringer Ingelheim International Gmbh Polymorphs
US9173859B2 (en) 2006-05-04 2015-11-03 Boehringer Ingelheim International Gmbh Uses of DPP IV inhibitors
US10080754B2 (en) 2006-05-04 2018-09-25 Boehringer Ingelheim International Gmbh Uses of DPP IV inhibitors
US11919903B2 (en) 2006-05-04 2024-03-05 Boehringer Ingelheim International Gmbh Polymorphs
US9815837B2 (en) 2006-05-04 2017-11-14 Boehringer Ingelheim International Gmbh Polymorphs
US9266888B2 (en) 2006-05-04 2016-02-23 Boehringer Ingelheim International Gmbh Polymorphs
US8673927B2 (en) 2006-05-04 2014-03-18 Boehringer Ingelheim International Gmbh Uses of DPP-IV inhibitors
US11291668B2 (en) 2006-05-04 2022-04-05 Boehringer Ingelheim International Gmbh Uses of DPP IV inhibitors
US10301313B2 (en) 2006-05-04 2019-05-28 Boehringer Ingelheim International Gmbh Polymorphs
US10973827B2 (en) 2008-04-03 2021-04-13 Boehringer Ingelheim International Gmbh DPP-IV inhibitor combined with a further antidiabetic agent, tablets comprising such formulations, their use and process for their preparation
US9415016B2 (en) 2008-04-03 2016-08-16 Boehringer Ingelheim International Gmbh DPP-IV inhibitor combined with a further antidiabetic agent, tablets comprising such formulations, their use and process for their preparation
US9155705B2 (en) 2008-04-03 2015-10-13 Boehringer Ingelheim International Gmbh DPP-IV inhibitor combined with a further antidiabetic agent, tablets comprising such formulations, their use and process for their preparation
US10022379B2 (en) 2008-04-03 2018-07-17 Boehringer Ingelheim International Gmbh DPP-IV inhibitor combined with a further antidiabetic agent, tablets comprising such formulations, their use and process for their preparation
US9486526B2 (en) 2008-08-06 2016-11-08 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients inappropriate for metformin therapy
US10034877B2 (en) 2008-08-06 2018-07-31 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients inappropriate for metformin therapy
US8853156B2 (en) 2008-08-06 2014-10-07 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients inappropriate for metformin therapy
US11911388B2 (en) 2008-10-16 2024-02-27 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral or non-oral antidiabetic drug
US9212183B2 (en) 2008-12-23 2015-12-15 Boehringer Ingelheim International Gmbh Salt forms of 1-[(4-methyl-quinazolin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-(3-(R)-amino-piperidin-1-yl)-xanthine
US8865729B2 (en) 2008-12-23 2014-10-21 Boehringer Ingelheim International Gmbh Salt forms of a xanthine compound
US8846695B2 (en) 2009-01-07 2014-09-30 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients with inadequate glycemic control despite metformin therapy comprising a DPP-IV inhibitor
US10092571B2 (en) 2009-11-27 2018-10-09 Boehringer Ingelheim International Gmbh Treatment of genotyped diabetic patients with DPP-IV inhibitors such as linagliptin
US9457029B2 (en) 2009-11-27 2016-10-04 Boehringer Ingelheim International Gmbh Treatment of genotyped diabetic patients with DPP-IV inhibitors such as linagliptin
US10004747B2 (en) 2010-05-05 2018-06-26 Boehringer Ingelheim International Gmbh Combination therapy
US9603851B2 (en) 2010-05-05 2017-03-28 Boehringer Ingelheim International Gmbh Combination therapy
US9186392B2 (en) 2010-05-05 2015-11-17 Boehringer Ingelheim International Gmbh Combination therapy
US9149478B2 (en) 2010-06-24 2015-10-06 Boehringer Ingelheim International Gmbh Diabetes therapy
US9034883B2 (en) 2010-11-15 2015-05-19 Boehringer Ingelheim International Gmbh Vasoprotective and cardioprotective antidiabetic therapy
US11911387B2 (en) 2010-11-15 2024-02-27 Boehringer Ingelheim International Gmbh Vasoprotective and cardioprotective antidiabetic therapy
US8962636B2 (en) 2011-07-15 2015-02-24 Boehringer Ingelheim International Gmbh Substituted quinazolines, the preparation thereof and the use thereof in pharmaceutical compositions
US9199998B2 (en) 2011-07-15 2015-12-01 Boehringer Ingelheim Internatioal Gmbh Substituted quinazolines, the preparation thereof and the use thereof in pharmaceutical compositions
US8883800B2 (en) 2011-07-15 2014-11-11 Boehringer Ingelheim International Gmbh Substituted quinazolines, the preparation thereof and the use thereof in pharmaceutical compositions
US9555001B2 (en) 2012-03-07 2017-01-31 Boehringer Ingelheim International Gmbh Pharmaceutical composition and uses thereof
US10195203B2 (en) 2012-05-14 2019-02-05 Boehringr Ingelheim International GmbH Use of a DPP-4 inhibitor in podocytes related disorders and/or nephrotic syndrome
US9526730B2 (en) 2012-05-14 2016-12-27 Boehringer Ingelheim International Gmbh Use of a DPP-4 inhibitor in podocytes related disorders and/or nephrotic syndrome
US9713618B2 (en) 2012-05-24 2017-07-25 Boehringer Ingelheim International Gmbh Method for modifying food intake and regulating food preference with a DPP-4 inhibitor
US9526728B2 (en) 2014-02-28 2016-12-27 Boehringer Ingelheim International Gmbh Medical use of a DPP-4 inhibitor
AU2014280955B2 (en) * 2014-12-24 2021-07-22 Arctic Ice Project Generation and deployment of ice with modified optical and/or thermal properties
US10155000B2 (en) 2016-06-10 2018-12-18 Boehringer Ingelheim International Gmbh Medical use of pharmaceutical combination or composition
US20230075532A1 (en) * 2021-08-31 2023-03-09 Tsinghua University Ice rink and method for making ice surface of ice rink

Also Published As

Publication number Publication date
AT503443A4 (de) 2007-10-15
RU2009102028A (ru) 2010-07-27
WO2007147185A1 (fr) 2007-12-27
AT503443B1 (de) 2007-10-15
CA2655336A1 (fr) 2007-12-27
EP2041234A1 (fr) 2009-04-01

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