JPH04263865A - Hardener for hydraulic cast - Google Patents
Hardener for hydraulic castInfo
- Publication number
- JPH04263865A JPH04263865A JP3045696A JP4569691A JPH04263865A JP H04263865 A JPH04263865 A JP H04263865A JP 3045696 A JP3045696 A JP 3045696A JP 4569691 A JP4569691 A JP 4569691A JP H04263865 A JPH04263865 A JP H04263865A
- Authority
- JP
- Japan
- Prior art keywords
- hydraulic
- cast
- curing agent
- water
- hardener
- 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
- 239000004848 polyfunctional curative Substances 0.000 title abstract 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229920000768 polyamine Polymers 0.000 claims abstract description 12
- 239000000835 fiber Substances 0.000 claims abstract description 6
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 4
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 4
- 229920005862 polyol Polymers 0.000 claims abstract description 4
- 150000003077 polyols Chemical class 0.000 claims abstract description 4
- 239000011347 resin Substances 0.000 claims abstract description 3
- 229920005989 resin Polymers 0.000 claims abstract description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 12
- 238000005266 casting Methods 0.000 claims description 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 3
- 201000010099 disease Diseases 0.000 abstract description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 3
- 230000000399 orthopedic effect Effects 0.000 abstract description 3
- 229920000642 polymer Polymers 0.000 abstract description 3
- 238000000465 moulding Methods 0.000 abstract 2
- 208000010392 Bone Fractures Diseases 0.000 abstract 1
- 206010024453 Ligament sprain Diseases 0.000 abstract 1
- 208000010040 Sprains and Strains Diseases 0.000 abstract 1
- 208000027418 Wounds and injury Diseases 0.000 abstract 1
- 238000004321 preservation Methods 0.000 abstract 1
- 238000007789 sealing Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 description 14
- 239000011342 resin composition Substances 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 5
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000008034 disappearance Effects 0.000 description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- -1 amine compound Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 229940098779 methanesulfonic acid Drugs 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- GTEXIOINCJRBIO-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]-n,n-dimethylethanamine Chemical compound CN(C)CCOCCN(C)C GTEXIOINCJRBIO-UHFFFAOYSA-N 0.000 description 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Materials For Medical Uses (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、整形外科的疾患の骨折
、捻性、脱臼部位の固定、或いはスポーツ時の体の保護
等のために体の所定部位に巻いたり添えたりして使用さ
れる水硬性キャストを硬化させるための硬化剤に関する
。[Industrial Application Field] The present invention can be used by wrapping or attaching to a predetermined part of the body to fix fractures, torsions, or dislocations in orthopedic diseases, or to protect the body during sports. This invention relates to a curing agent for curing hydraulic cast.
【0002】0002
【従来の技術】整形外科的疾患の部位の固定、支持、保
護のため、ポリイソシアネートとポリオールとからなる
ウレタンプレポリマーを主成分とし、触媒、安定剤、消
泡剤、着色剤等を配合した水硬性ウレタン樹脂組成物を
ガラス繊維、ポリエステル繊維、アラミド繊維、線繊維
等の繊維からなる比較的目の粗い編物、織物の基布に含
浸塗布した水硬性キャストを湿気不透過性の袋に封入し
ておき、使用の際袋より水硬性キャストを取り出して水
に漬け、使用部位に巻いたり添えたりして硬化させるこ
とは既に知られている。この水硬性キャストは水分との
反応性が高く長期保存に問題があり、製造条件、包装材
料、配合面等の種々の技術が提案されているが、いずれ
も満足すべきものではない。例えば、製造条件では使用
する基材を前もって乾燥し基材中の水分を極限近くまで
取り除き、水分量100ppm 以下の雰囲気で塗布す
る技術、包装材料としてナイロン、アルミニウム、ポリ
プロピレンからなる複合フィルムによる完全な湿気不透
過性素材を使用し、袋に窒素ガスと置換して封入する技
術、配合面ではウレタンプレポリマーと触媒や硬化剤を
分離し、使用時に接触させるようにしたもの、触媒、安
定剤の種類、両者の組合わせの種類を選択する技術等が
提案されている。しかしながら製造面で対応しようとす
る技術は設備スペース、設備費、環境維持費が大となる
問題点があり、ウレタンプレポリマーと触媒や硬化剤を
分離させたものは保存安定性は良好であるが使用時ウレ
タンプレポリマーと触媒とを均等に接触させることが難
しく硬化がむらになる欠点がある。また触媒や安定剤を
選択する方法は保存安定性はかなり改善されるがなお満
足すべきものではない。すなわち保存安定性を高めよう
として触媒の量を少なくしたり触媒作用の緩慢なものを
使用したり、或いは安定剤の配合量を増加させると、保
存安定性は向上するが使用時の硬化時間が長くなり、逆
にすると硬化時間は短くなるが保存安定性は低下し、保
存安定性と硬化時間の両者を満足させることができない
。[Prior Art] In order to fix, support and protect the site of orthopedic disease, a urethane prepolymer consisting of polyisocyanate and polyol is the main component, and a catalyst, stabilizer, antifoaming agent, coloring agent, etc. are mixed therein. A hydraulic cast made by impregnating and applying a hydraulic urethane resin composition to a relatively coarse knitted or woven base fabric made of fibers such as glass fibers, polyester fibers, aramid fibers, and wire fibers is enclosed in a moisture-impermeable bag. It is already known that the hydraulic cast is removed from the bag before use, soaked in water, and then wrapped or attached to the area of use to harden. This hydraulic cast is highly reactive with moisture and has problems in long-term storage. Various techniques have been proposed regarding manufacturing conditions, packaging materials, compounding aspects, etc., but none of them are satisfactory. For example, the manufacturing conditions include a technology in which the base material to be used is dried in advance to remove as much water as possible in the base material, and then applied in an atmosphere with a moisture content of 100 ppm or less; Technology that uses a moisture-impermeable material and encloses it in a bag after replacing it with nitrogen gas.In terms of compounding, the urethane prepolymer is separated from the catalyst and curing agent so that they come into contact with each other during use. Techniques for selecting types and combinations of the two have been proposed. However, the technology that attempts to respond to this from a manufacturing perspective has the problem of large equipment space, equipment costs, and environmental maintenance costs, and products in which the urethane prepolymer is separated from the catalyst and curing agent have good storage stability. During use, it is difficult to bring the urethane prepolymer into even contact with the catalyst, resulting in uneven curing. Furthermore, although the storage stability is considerably improved by the method of selecting catalysts and stabilizers, it is still not satisfactory. In other words, if you reduce the amount of catalyst or use a catalyst with slow catalytic action in an attempt to improve storage stability, or increase the amount of stabilizer blended, storage stability will improve, but the curing time during use will decrease. Conversely, the curing time becomes shorter, but the storage stability decreases, making it impossible to satisfy both storage stability and curing time.
【0003】0003
【発明が解決しようとする課題】本発明の目的は、保存
安定性を高め、通常の水硬性キャストと同様の設備、環
境条件で製造することができ、しかも十分満足のいく時
間内で硬化させることのできる水硬性キャスト用硬化剤
を提供することにある。[Problems to be Solved by the Invention] The object of the present invention is to improve storage stability, to be able to manufacture the product using the same equipment and environmental conditions as ordinary hydraulic casting, and to cure within a sufficiently satisfactory time. An object of the present invention is to provide a curing agent for hydraulic casting that can be used for hydraulic casting.
【0004】0004
【課題を解決するための手段】上記の目的を達成するた
め、本発明においては、ポリオールとポリイソシアネー
トからなるウレタンプレポリマーを主成分とする水硬化
性樹脂を繊維形成物に塗布し、湿気不透過性の袋に封入
した水硬性キャストを硬化させるための硬化剤が水溶性
ポリアミン化合物を含有するものである。[Means for Solving the Problems] In order to achieve the above object, in the present invention, a water-curable resin whose main component is a urethane prepolymer made of polyol and polyisocyanate is coated on a fiber formed product to prevent moisture. A curing agent for curing the hydraulic cast sealed in a permeable bag contains a water-soluble polyamine compound.
【0005】水溶性ポリアミン化合物が1級アミノ基、
2級アミノ基、又はこれらを1分子内に2個以上有する
ものであるのが好ましい。[0005] The water-soluble polyamine compound has a primary amino group,
It is preferable to have a secondary amino group or two or more of these in one molecule.
【0006】ポリアミン化合物を5%以上含有する水溶
液として硬化剤を形成するのが有利である。It is advantageous to form the curing agent as an aqueous solution containing more than 5% of the polyamine compound.
【0007】本発明による硬化剤を水硬性キャストに適
用する方法としては、ポリアミン化合物を含有する水溶
液に直接水硬性キャストを浸漬して接触させる方法、こ
の水溶液を噴霧状または泡状にして水硬性キャスト上に
塗布する方法などを用いることがてきる。Methods for applying the curing agent according to the present invention to hydraulic casts include a method in which the hydraulic cast is directly immersed in an aqueous solution containing a polyamine compound to contact it, and a method in which the aqueous solution is sprayed or foamed to form a hydraulic cast. A method such as applying it on a cast can be used.
【0008】[0008]
【作用】本発明の水硬性キャスト用硬化剤がキャストの
ポリウレタンプレポリマーと接触すると、ポリアミン化
合物のアミノ基とウレタンプレポリマーのイソシアネー
ト基が反応して尿素結合を造り高分子に成長する反応と
、ウレタンプレポリマーのイソシアネート基と水とが反
応してウレタン結合を造り、カルバミン酸、二酸化炭素
及びアミン化合物を生成し、さらにこのアミン中間化合
物はイソシアネート基と反応し、尿素結合を造りながら
高分子になる反応とが生じる。ウレタンプレポリマーの
イソシアネートは、ポリアミン化合物と水とでは、ポリ
アミン化合物との方が反応性が高く、選択的にポリアミ
ン化合物と反応し高分子化すなわち硬化して行くため、
硬化時間が短絡される。[Operation] When the hydraulic casting curing agent of the present invention comes into contact with the cast polyurethane prepolymer, the amino groups of the polyamine compound and the isocyanate groups of the urethane prepolymer react to form urea bonds and grow into a polymer. The isocyanate groups of the urethane prepolymer react with water to create urethane bonds, producing carbamic acid, carbon dioxide, and an amine compound.Furthermore, this amine intermediate compound reacts with the isocyanate groups to form a polymer while creating urea bonds. A reaction occurs. The isocyanate of the urethane prepolymer has higher reactivity with the polyamine compound than with water, and selectively reacts with the polyamine compound to polymerize, that is, harden.
Curing time is shortened.
【0009】[0009]
【実施例】次に本発明の実施例を説明する。[Example] Next, an example of the present invention will be described.
【0010】A1.樹脂組成物
MDIと平均分子量850のPPGとを反応させてウレ
タンプレポリマーを合成し、これにビスフェノールAを
15.8%、TDMMEA〔トリ(2,6‐ジメチルモ
ルホリノエチル)アミン〕を2.8%、MSA(メタン
スルホン酸)を0.03%、PEG(ポリエチレングリ
コール)を0.4%添加し、樹脂組成物を造った。A1. A urethane prepolymer was synthesized by reacting the resin composition MDI with PPG having an average molecular weight of 850, and to this was added 15.8% of bisphenol A and 2.8% of TDMMEA [tri(2,6-dimethylmorpholinoethyl)amine]. %, 0.03% MSA (methane sulfonic acid) and 0.4% PEG (polyethylene glycol) were added to prepare a resin composition.
【0011】A2.樹脂組成物
MDIと平均分子量700のPPGとを反応させてウレ
タンプレポリマーを合成し、これに触媒としてビス(N
,N‐ジメチルアミノエチル)エーテルを1.5%、安
定剤としてベンゾイルクロライドを0.2%、酸化防止
剤としてイルガノックス1100(商品名)を0.2%
、消泡剤としてシリコン系のものを0.1%混合して樹
脂組成物を造った。この樹脂組成物はA1のものに比し
触媒の量が少なく、約1.7倍のシェルフライフを有す
るものである。A2. A urethane prepolymer is synthesized by reacting the resin composition MDI with PPG having an average molecular weight of 700, and bis(N
, N-dimethylaminoethyl) ether (1.5%), benzoyl chloride (0.2%) as a stabilizer, and Irganox 1100 (trade name) as an antioxidant (0.2%).
A resin composition was prepared by mixing 0.1% of a silicone-based antifoaming agent. This resin composition has a smaller amount of catalyst than A1 and has a shelf life about 1.7 times longer.
【0012】B.評価検体
ガラス繊維をラッシェル編でテープ状に作成した目付量
340g/m2の目の粗い基布に、上述のいずれかの樹
脂組成物を低湿度条件で230g/m2塗布し、3m
の長さに巻き取ってロールとし、アルミフィルム、ナイ
ロン、ポリプロピレンのラミネートからなる高防水性の
袋に窒素置換後挿入し、熱シールで密封し評価検体とし
た。B. Evaluation sample One of the above-mentioned resin compositions was applied at 230 g/m2 under low humidity conditions to a coarse base fabric with a basis weight of 340 g/m2 made of glass fibers made into a tape shape by Raschel knitting, and a 3 m
The sample was wound up into a roll, replaced with nitrogen, inserted into a highly waterproof bag made of a laminate of aluminum film, nylon, and polypropylene, and sealed with a heat seal to serve as an evaluation sample.
【0013】C1.硬化剤
1級アミンとして炭酸グアニジン、2級アミンとしてピ
ペラジン、1級と2級アミンを含むものとして3‐アミ
ノ‐1,2,4‐トリアゾールをそれぞれ水に溶解して
硬化剤を造った。C1. Hardening agents A hardening agent was prepared by dissolving guanidine carbonate as a primary amine, piperazine as a secondary amine, and 3-amino-1,2,4-triazole as a material containing primary and secondary amines in water.
【0014】C2.硬化剤 比較のため従来使用されている水を硬化剤とした。C2. hardening agent For comparison, water, which is conventionally used, was used as a curing agent.
【0015】次表は本発明の実施例と比較例とについて
タック消失時間と硬化時間について評価したもので、実
施例1〜9はA1に示す樹脂組成物を使用してBに示す
評価検体を作り、C1の硬化剤の種々の濃度について評
価した例、比較例1は同じ評価検体について硬化剤とし
てC2の水を使用した場合の例、実施例10はA2に示
す樹脂組成物を使用してBに示す評価検体を作り、C1
の硬化剤について評価した例、比較例2はその同じ評価
検体について硬化剤としてC2の水を使用した場合であ
る。[0015] The following table shows the evaluation of tack disappearance time and curing time for Examples and Comparative Examples of the present invention. In Examples 1 to 9, the evaluation specimen shown in B was prepared using the resin composition shown in A1. Comparative Example 1 is an example in which C2 water is used as a curing agent for the same evaluation sample, and Example 10 is an example in which the resin composition shown in A2 is used. Prepare the evaluation sample shown in B, and
Comparative Example 2 is an example in which the curing agent was evaluated using C2 water as the curing agent for the same evaluation specimen.
【0016】試験方法は、検体を袋より取り出し、剥離
紙上にて3層に重ね硬化剤液をかけ、指触により表面の
べたつきが消失するまでの時間を計りタック消失時間と
した。又、4層に折り重ねた検体を10cm×15cm
にカットし、硬化剤をつけたものが硬化して形状が保持
できるまでの時間を計り硬化時間とした。[0016] The test method was to take a sample out of the bag, stack it on release paper in three layers, apply a hardening agent solution, and measure the time until the stickiness on the surface disappeared when touched with a finger, which was determined as the tack disappearance time. In addition, the specimen was folded in 4 layers to a size of 10 cm x 15 cm.
The curing time was determined by measuring the time it took for the piece to be cut and coated with a hardening agent to harden and retain its shape.
【0017】試験結果によれば、本発明による硬化剤は
タック消失時間も硬化時間も極めて良好であり、硬化剤
濃度は20〜30%が好ましく、それ以上濃度を高くし
ても効果の著しい上昇はなく、一方着色性が増し、溶解
性にも多少問題が出てくる。According to the test results, the curing agent according to the present invention has extremely good tack disappearance time and curing time, and the curing agent concentration is preferably 20 to 30%, and even if the concentration is higher than that, the effect increases significantly. On the other hand, the coloring property increases and there are some problems with solubility.
【0018】[0018]
【表1】[Table 1]
【0019】[0019]
【発明の効果】本発明によれば、水硬性キャストの硬化
時間を短縮できるから、従来活性の高い種類の触媒を配
合したり、触媒の配合量を多くして対応してきた技術が
不要となり、活性の低い触媒を使用したり触媒の配合量
を少なくすることができ、水硬性キャストの保存安定性
は高くなる。さらにこの活性の低い触媒を利用でき、触
媒の配合量を少なくすることができることは水硬性キャ
ストの製造条件の緩和に結び付くものである。[Effects of the Invention] According to the present invention, since the curing time of hydraulic cast can be shortened, the conventional techniques of blending highly active catalysts or increasing the amount of catalyst blended are no longer necessary. It is possible to use a catalyst with low activity or to reduce the amount of catalyst blended, and the storage stability of the hydraulic cast is increased. Furthermore, the fact that this low-activity catalyst can be used and the amount of catalyst blended can be reduced leads to relaxation of the manufacturing conditions for hydraulic casting.
【0020】又、本発明の硬化剤を従来の水硬性キャス
トに使用すると硬化時間が従来より短縮されるから、特
に硬化時間を短縮したい小児患者や矯正目的に利用する
場合に有利である。さらに、キャストを患部に適用した
後硬化剤を噴霧状又は泡状にして塗布し部分的に硬化さ
せるような使用方法も有利に可能となるものである。Furthermore, when the curing agent of the present invention is used in conventional hydraulic casts, the curing time is shorter than that of conventional castings, so it is particularly advantageous for pediatric patients who wish to shorten the curing time or for use in orthodontic purposes. Furthermore, after applying the cast to the affected area, it is possible to advantageously apply a hardening agent in the form of a spray or foam to partially harden the cast.
Claims (4)
なるウレタンプレポリマーを主成分とする水硬化性樹脂
を繊維形成物に塗布し湿気不透過性の袋に封入した水硬
性キャストを硬化させるための硬化剤が、水溶性ポリア
ミン化合物を含有することを特徴とする水硬性キャスト
用硬化剤。Claim 1: A curing agent for curing a hydraulic cast in which a hydraulic resin mainly composed of a urethane prepolymer consisting of polyol and polyisocyanate is applied to a fiber formed product and sealed in a moisture-impermeable bag. A curing agent for hydraulic casting, characterized by containing a water-soluble polyamine compound.
基を1分子内に2個以上有するものであることを特徴と
する請求項1記載の水硬性キャスト用硬化剤。2. The curing agent for hydraulic casting according to claim 1, wherein the water-soluble polyamine compound has two or more primary amino groups in one molecule.
基を1分子内に2個以上有するものであることを特徴と
する請求項1記載の水硬性キャスト用硬化剤。3. The curing agent for hydraulic casting according to claim 1, wherein the water-soluble polyamine compound has two or more secondary amino groups in one molecule.
基及び2級アミノ基を1分子内に合わせて2個以上有す
るものであることを特徴とする請求項1記載の水硬性キ
ャスト用硬化剤。4. The curing agent for hydraulic casting according to claim 1, wherein the water-soluble polyamine compound has two or more primary amino groups and two or more secondary amino groups in one molecule.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3045696A JP3014786B2 (en) | 1991-02-20 | 1991-02-20 | Hardener for hydraulic cast |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3045696A JP3014786B2 (en) | 1991-02-20 | 1991-02-20 | Hardener for hydraulic cast |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04263865A true JPH04263865A (en) | 1992-09-18 |
JP3014786B2 JP3014786B2 (en) | 2000-02-28 |
Family
ID=12726549
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3045696A Expired - Fee Related JP3014786B2 (en) | 1991-02-20 | 1991-02-20 | Hardener for hydraulic cast |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3014786B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06254146A (en) * | 1993-03-10 | 1994-09-13 | Arukea Kk | Hydraulic casting member |
JP2019513855A (en) * | 2016-03-29 | 2019-05-30 | ダウ グローバル テクノロジーズ エルエルシー | Adhesive Formulation for Lamination Comprising Polyurethane and Latent Catalyst |
-
1991
- 1991-02-20 JP JP3045696A patent/JP3014786B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06254146A (en) * | 1993-03-10 | 1994-09-13 | Arukea Kk | Hydraulic casting member |
JP2019513855A (en) * | 2016-03-29 | 2019-05-30 | ダウ グローバル テクノロジーズ エルエルシー | Adhesive Formulation for Lamination Comprising Polyurethane and Latent Catalyst |
Also Published As
Publication number | Publication date |
---|---|
JP3014786B2 (en) | 2000-02-28 |
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