JP2012210408A - Gel mat and method for producing same by ultraviolet light curing - Google Patents
Gel mat and method for producing same by ultraviolet light curing Download PDFInfo
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- JP2012210408A JP2012210408A JP2012072166A JP2012072166A JP2012210408A JP 2012210408 A JP2012210408 A JP 2012210408A JP 2012072166 A JP2012072166 A JP 2012072166A JP 2012072166 A JP2012072166 A JP 2012072166A JP 2012210408 A JP2012210408 A JP 2012210408A
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 18
- 239000000178 monomer Substances 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000003999 initiator Substances 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 claims abstract description 12
- IRLPACMLTUPBCL-KQYNXXCUSA-N 5'-adenylyl sulfate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OS(O)(=O)=O)[C@@H](O)[C@H]1O IRLPACMLTUPBCL-KQYNXXCUSA-N 0.000 claims abstract description 10
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 9
- 235000011187 glycerol Nutrition 0.000 claims abstract description 9
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 claims abstract description 9
- -1 alkali metal acrylates Chemical class 0.000 claims abstract description 8
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 claims abstract description 7
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims abstract description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- 150000002148 esters Chemical class 0.000 claims abstract description 7
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 7
- 125000002091 cationic group Chemical group 0.000 claims abstract description 4
- 238000001723 curing Methods 0.000 claims description 9
- 239000004744 fabric Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 238000003848 UV Light-Curing Methods 0.000 claims description 8
- 239000011521 glass Substances 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 238000004806 packaging method and process Methods 0.000 claims description 5
- 229920000742 Cotton Polymers 0.000 claims description 3
- 239000004677 Nylon Substances 0.000 claims description 3
- 229920004933 Terylene® Polymers 0.000 claims description 3
- 238000002347 injection Methods 0.000 claims description 3
- 239000007924 injection Substances 0.000 claims description 3
- 238000007689 inspection Methods 0.000 claims description 3
- 229920001778 nylon Polymers 0.000 claims description 3
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 239000000047 product Substances 0.000 description 17
- 229940048053 acrylate Drugs 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000005341 toughened glass Substances 0.000 description 5
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 3
- 239000011265 semifinished product Substances 0.000 description 3
- 229940047670 sodium acrylate Drugs 0.000 description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- 125000005520 diaryliodonium group Chemical group 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/58—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine
- C08F220/585—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine and containing other heteroatoms, e.g. 2-acrylamido-2-methylpropane sulfonic acid [AMPS]
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47C—CHAIRS; SOFAS; BEDS
- A47C27/00—Spring, stuffed or fluid mattresses or cushions specially adapted for chairs, beds or sofas
- A47C27/08—Fluid mattresses or cushions
- A47C27/085—Fluid mattresses or cushions of liquid type, e.g. filled with water or gel
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47G—HOUSEHOLD OR TABLE EQUIPMENT
- A47G27/00—Floor fabrics; Fastenings therefor
- A47G27/02—Carpets; Stair runners; Bedside rugs; Foot mats
- A47G27/0212—Carpets; Stair runners; Bedside rugs; Foot mats to support or cushion
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/56—Acrylamide; Methacrylamide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/36—Amides or imides
- C08F222/38—Amides
- C08F222/385—Monomers containing two or more (meth)acrylamide groups, e.g. N,N'-methylenebisacrylamide
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/23—Sheet including cover or casing
- Y10T428/239—Complete cover or casing
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Polymerisation Methods In General (AREA)
- Mattresses And Other Support Structures For Chairs And Beds (AREA)
- Invalid Beds And Related Equipment (AREA)
- Thermotherapy And Cooling Therapy Devices (AREA)
- Cosmetics (AREA)
Abstract
Description
本発明は、ゲルマットおよびその紫外線硬化製造方法に関する。 The present invention relates to a gel mat and a method for producing an ultraviolet curable product thereof.
近年、ゲルマット(gel mat)などに相応するいくつかの涼しいマット製品、例えば出願番号:200810063081.4などが市販されているが、涼しい時間が十分に長くなく、涼しい感覚があまり顕著でない問題が存在しており、また、この製品を製造する際に、製品の表面に比較的長い「凹痕」が生じること、内容物が外部包装材料に飛び散りやすく製品表面の汚れを引き起こすこと、封口する際に、袋中の空気が完全に押し出されないと、製品の表面に大きさの異なる多数の「窪み」が現われて外観に影響を与えること、製造過程でホットプレスする必要があるため、エネルギー消耗が多いこと、製品が製造された後、降温後に初めて包装できるため、プロセスが煩雑で、工場の敷地面積が大きいことなどという欠点が存在している。また、これらの方法は、例えば出願番号:200810063081.4のように、製造過程において、加熱硬化に必要な時間が長く、エネルギー消耗が大きく、効率も高くない。一部の方法では、エネルギー消耗がやや小さいが、硬化時間が5時間以上かかり、効率および現場の運営に深刻な影響を与える。また、高分子を用いて架橋成形された一部のゲルマットには強度が足りなく、ゲルの使用寿命が短く、変形しやすく、固形分が足りないなどという、製品の使用に非常に深刻な影響を与える欠点が見受けられる。 In recent years, some cool mat products corresponding to gel mats and the like, for example, application number: 200810063081.4, are commercially available, but there is a problem that the cool time is not long enough and the cool sensation is not so noticeable. In addition, when manufacturing this product, relatively long “dents” are formed on the surface of the product, the contents are likely to be scattered on the external packaging material, and the product surface is soiled. If the air in the bag is not completely pushed out, many “dents” of different sizes appear on the surface of the product, affecting the appearance, and it is necessary to perform hot pressing during the manufacturing process. There are many disadvantages, such as the fact that the product can be packaged for the first time after the product has cooled down, and the process is complicated and the site area of the factory is large. It is. Further, these methods, for example, as in application number: 200810063081.4, require a long time for heat curing in the production process, consume large energy, and do not have high efficiency. Some methods consume slightly less energy, but take more than 5 hours to cure, seriously affecting efficiency and field operations. In addition, some gel mats cross-linked with polymers are not strong enough, the gel has a short service life, is easily deformed, lacks solids, etc. There are some drawbacks.
本発明の目的は、ゲルマットを製造する従来技術に存在する上記課題を解決して、ゲルマットおよびその紫外線硬化製造方法を提供することである。 The object of the present invention is to solve the above-mentioned problems existing in the prior art for producing a gel mat, and to provide a gel mat and a method for producing an ultraviolet ray thereof.
上記の課題を解決するために、本発明では、モノマーと、架橋剤と、光開始剤と、水とを紫外線により硬化してなるゲルをゲル袋内に装填することを特徴とする、ゲル袋を備えるゲルマットおよびその紫外線硬化製造方法が設計される。前記ゲルが、百分率で、下記の組成物:
モノマー 5〜30%、
架橋剤 0.01〜2%、
光開始剤 0.001〜2%、
残部の水ならなることを特徴とする。
In order to solve the above problems, the present invention provides a gel bag characterized in that a gel formed by curing a monomer, a crosslinking agent, a photoinitiator, and water with ultraviolet rays is loaded into the gel bag. And a UV curable manufacturing method thereof are designed. The gel is, as a percentage, the following composition:
5-30% monomer,
Cross-linking agent 0.01-2%,
0.001-2% photoinitiator,
It is characterized by the remaining water.
前記モノマーが、アクリル酸アルカリ金属塩、メタクリル酸から生成したエステル、アクリルアミド、メタクリルアミド、AMPS(2−アクリルアミド−2−メチルプロパンスルホン酸)のうちの2種または2種以上の組成物であることを特徴とする。前記架橋剤が、複数の非共役二重結合を有する化合物であって、多価アルコール(グリセリン)、N,N’−メチレンビスアクリルアミドであることを特徴とする。前記光開始剤が、分解型開始剤または感熱性開始剤またはカチオン性開始剤であることを特徴とする。前記ゲル袋の外層が、綿布またはナイロン布またはテリレン布であり、内層がPVCフィルムまたはTPUフィルムまたはPEフィルムまたはEVAフィルムであることを特徴とする。ゲルマットの紫外線硬化製造方法は、ゲル袋の作製、注入、封口、紫外線硬化、検査包装の5つのステップからなり、紫外線硬化過程において、注入、封口されたゲル袋に一定の圧力を加えて、ゲル袋の両側を挟んだ2枚の強化ガラスまたは石英ガラスでゲル袋をプレスして平らにし、紫外線の単位面積当たりの照射強度が50mJ/cm2〜5000mJ/cm2で、硬化時間が10秒〜60分であり、コンベアによりガラスでプレスしたゲル袋半製品を搬送し、紫外線区間を経過した後に出したものが初期製品となり、仕上げ処理後に検査包装することを特徴とする。 The monomer is a composition of two or more of an alkali metal acrylate, an ester formed from methacrylic acid, acrylamide, methacrylamide, and AMPS (2-acrylamido-2-methylpropanesulfonic acid). It is characterized by. The cross-linking agent is a compound having a plurality of non-conjugated double bonds, and is a polyhydric alcohol (glycerin) or N, N′-methylenebisacrylamide. The photoinitiator is a decomposable initiator, a heat-sensitive initiator, or a cationic initiator. The outer layer of the gel bag is a cotton cloth, a nylon cloth, or a terylene cloth, and the inner layer is a PVC film, a TPU film, a PE film, or an EVA film. The UV curing method of gel mat consists of five steps: preparation of gel bag, injection, sealing, UV curing, and inspection packaging. In the UV curing process, a certain pressure is applied to the injected and sealed gel bag to The gel bag is pressed and flattened with two sheets of tempered glass or quartz glass sandwiched on both sides of the bag, the irradiation intensity per unit area of ultraviolet light is 50 mJ / cm 2 to 5000 mJ / cm 2 , and the curing time is 10 seconds to It is 60 minutes, and is characterized in that a semi-finished gel bag product that is pressed with glass by a conveyor is transported, and the product that is taken out after passing through the ultraviolet section becomes the initial product and is inspected and packaged after finishing treatment.
本発明は、製造工程が簡単で、ゲルの硬化が速く、作製したゲルマットが滑らかであることを特徴とする。 The present invention is characterized in that the production process is simple, the gel hardens quickly, and the gel mat produced is smooth.
図中にゲル袋が含まれ、ゲル袋内にゲル2が装填されており、前記ゲルがモノマーと、架橋剤と、光開始剤と、水とを紫外線により硬化してなることを特徴とする。前記ゲルが、百分率で、下記の組成物:
モノマー 5〜30%、
架橋剤 0.01〜2%、
光開始剤 0.001〜2%、
残部の水からなることを特徴とする。
The gel bag is included in the figure, the
5-30% monomer,
Cross-linking agent 0.01-2%,
0.001-2% photoinitiator,
It consists of the remaining water.
前記モノマーが、アクリル酸アルカリ金属塩、メタクリル酸から生成したエステル、アクリルアミド、メタクリルアミド、AMPS(2−アクリルアミド−2−メチルプロパンスルホン酸)のうちの2種または2種以上の組成物であることを特徴とする。前記架橋剤が、複数の非共役二重結合を有する化合物であって、多価アルコール(グリセリン)、N,N’−メチレンビスアクリルアミドであることを特徴とする。前記光開始剤が、分解型開始剤または感熱性開始剤またはカチオン性開始剤であることを特徴とする。前記ゲル袋の外層が、綿布またはナイロン布またはテリレン布であり、内層がPVCフィルムまたはTPUフィルムまたはPEフィルムまたはEVAフィルムであることを特徴とする。ゲルマットの紫外線硬化製造方法は、ゲル袋の作製、注入、封口、紫外線硬化、検査包装の5つのステップからなり、紫外線硬化過程において、注入、封口されたゲル袋に一定の圧力を加えて、ゲル袋の両側を挟んだ2枚の強化ガラスまたは石英ガラスでゲル袋をプレスして平らにし、紫外線の単位面積当たりの照射強度が50mJ/cm2〜5000mJ/cm2で、硬化時間が10秒〜60分であり、コンベアによりガラスでプレスしたゲル袋半製品を搬送し、紫外線区間を経過した後に出したものが初期製品となり、仕上げ処理後に検査包装することを特徴とする。 The monomer is a composition of two or more of an alkali metal acrylate, an ester formed from methacrylic acid, acrylamide, methacrylamide, and AMPS (2-acrylamido-2-methylpropanesulfonic acid). It is characterized by. The cross-linking agent is a compound having a plurality of non-conjugated double bonds, and is a polyhydric alcohol (glycerin) or N, N′-methylenebisacrylamide. The photoinitiator is a decomposable initiator, a heat-sensitive initiator, or a cationic initiator. The outer layer of the gel bag is a cotton cloth, a nylon cloth, or a terylene cloth, and the inner layer is a PVC film, a TPU film, a PE film, or an EVA film. The UV curing method of gel mat consists of five steps: preparation of gel bag, injection, sealing, UV curing, and inspection packaging. In the UV curing process, a certain pressure is applied to the injected and sealed gel bag to The gel bag is pressed and flattened with two sheets of tempered glass or quartz glass sandwiched on both sides of the bag, the irradiation intensity per unit area of ultraviolet light is 50 mJ / cm 2 to 5000 mJ / cm 2 , and the curing time is 10 seconds to It is 60 minutes, and is characterized in that a semi-finished gel bag product that is pressed with glass by a conveyor is transported, and the product that is taken out after passing through the ultraviolet section becomes the initial product and is inspected and packaged after finishing treatment.
実施例1
モノマー5kg、架橋剤0.01kg、光開始剤0.001kg、水94.989kgを取ってゲル原料100kgを配合し、用いられたモノマーは、アクリル酸アルカリ金属塩、メタクリル酸から生成したエステル、アクリルアミド、メタクリルアミド、AMPS(2−アクリルアミド−2−メチルプロパンスルホン酸)のうちの2種または2種以上の組成物、例えば、アクリル酸ナトリウムとAMPSとを3:1で配合された混合物であった。用いられた架橋剤は、複数の非共役二重結合を有する化合物であって、多価アルコール(グリセリン)、N,N’−メチレンビスアクリルアミド、例えば、グリセリンであり、用いられた光開始剤は、BP(Benzophenone、ベンゾフェノン、江陰ムーア化工、光開始剤BPと呼ばれる)であり、水は純水であり、配合したゲル原料を作製されたゲル袋に注入し、排気後に加熱して封口し、2枚の強化ガラスまたは石英ガラスでゲル袋をプレスして平らにし、コンベアによりガラスでプレスしたゲル袋半製品を、紫外線の単位面積当たりの照射強度が50mJ/cm2〜5000mJ/cm2で、硬化時間が60分である紫外線照射機に搬送して硬化させ、最後にコンベアにより紫外線区間を経過したゲルマットの初期製品を送出し、バリ取り後に検査包装した。
Example 1
5 kg of monomer, 0.01 kg of crosslinking agent, 0.001 kg of photoinitiator, 94.989 kg of water and 100 kg of gel raw material were blended, and the monomers used were alkali metal acrylate, ester formed from methacrylic acid, acrylamide , Methacrylamide, AMPS (2-acrylamido-2-methylpropanesulfonic acid), or two or more compositions, for example, a mixture of sodium acrylate and AMPS in a ratio of 3: 1 . The used crosslinking agent is a compound having a plurality of non-conjugated double bonds, and is a polyhydric alcohol (glycerin), N, N′-methylenebisacrylamide, for example, glycerin, and the photoinitiator used is BP (Benzophenone, Benzophenone, Jiangyin Moore Chemical, photoinitiator BP), water is pure water, the blended gel raw material is poured into the prepared gel bag, heated and sealed after evacuation, the gel bag flattened and pressed by two tempered glass or quartz glass, gel bags semifinished product was pressed by a glass by a conveyor, the irradiation intensity per unit area of the ultraviolet rays at 50mJ / cm 2 ~5000mJ / cm 2 , It is transported to an ultraviolet irradiator with a curing time of 60 minutes and cured, and finally the initial gel mat product that has passed the ultraviolet section is delivered by a conveyor. Then, after deburring, it was inspected and packaged.
実施例2
モノマー22kg、架橋剤1kg、光開始剤1kg、水76kgを取ってゲル原料100kgを配合し、用いられたモノマーは、アクリル酸アルカリ金属塩、メタクリル酸から生成したエステル、アクリルアミド、メタクリルアミド、AMPS(2−アクリルアミド−2−メチルプロパンスルホン酸)のうちの2種または2種以上の組成物、例えば、アクリル酸ナトリウム、アクリルアミドおよびAMPSが3:1:1の割合で配合された混合物であった。用いられた架橋剤は、複数の非共役二重結合を有する化合物であって、多価アルコール(グリセリン)、N,N’−メチレンビスアクリルアミド、例えば、N,N’−メチレンビスアクリルアミドであり、用いられた光開始剤は、市販の光開始剤184(Methanone、1−ヒドロキシシクロヘキシルフェニルケトン、江陰ムーア化工)であり、水は純水であり、配合したゲル原料を作製されたゲル袋に注入し、排気後に加熱して封口し、2枚の強化ガラスまたは石英ガラスでゲル袋をプレスして平らにし、コンベアによりガラスでプレスしたゲル袋半製品を、紫外線の単位面積当たりの照射強度が50mJ/cm2〜5000mJ/cm2で、硬化時間が3分である紫外線照射機に搬送して硬化させ、最後にコンベアにより紫外線区間を経過したゲルマットの初期製品を送出し、バリ取り後に検査包装した。
Example 2
Monomer 22 kg, cross-linking agent 1 kg, photoinitiator 1 kg, water 76 kg were taken and 100 kg of gel raw material was blended. Monomers used were alkali metal acrylate, ester formed from methacrylic acid, acrylamide, methacrylamide, AMPS ( 2-acrylamido-2-methylpropanesulfonic acid), or a mixture of sodium acrylate, acrylamide and AMPS in a ratio of 3: 1: 1. The cross-linking agent used is a compound having a plurality of non-conjugated double bonds, and is a polyhydric alcohol (glycerin), N, N′-methylenebisacrylamide, for example, N, N′-methylenebisacrylamide, The photoinitiator used is a commercially available photoinitiator 184 (Methanone, 1-hydroxycyclohexyl phenyl ketone, Jiangyin Moore Chemical), water is pure water, and the blended gel material is injected into the prepared gel bag The gel bag is heated and sealed after evacuation, the gel bag is pressed and flattened with two sheets of tempered glass or quartz glass, and the gel bag semi-finished product pressed with glass by a conveyor has an irradiation intensity of 50 mJ per unit area of ultraviolet rays. / cm 2 at ~5000MJ / cm 2, and cured by conveyor UV irradiator curing time is 3 minutes, finally ultraviolet ku by the conveyor It sends the initial product of Gerumatto have elapsed, and examined the packaging after the deburring.
実施例3
モノマー30kg、架橋剤2kg、光開始剤2kg、水66kgを取ってゲル原料100kgを配合し、用いられたモノマーは、アクリル酸アルカリ金属塩、メタクリル酸から生成したエステル、アクリルアミド、メタクリルアミド、AMPS(2−アクリルアミド−2−メチルプロパンスルホン酸)のうちの2種または2種以上の組成物、例えば、アクリルアミド:AMPS:アクリル酸ナトリウム:メタクリルアミドが5:1:2:1の混合物であった。用いられた架橋剤は、複数の非共役二重結合を有する化合物であって、多価アルコール(グリセリン)、N,N’−メチレンビスアクリルアミド、例えば、グリセリンとN,N’−メチレンビスアクリルアミドとの混合物であり、用いられた光開始剤は、通常使用される市販のジアリールヨードニウム塩(米国GE社)であり、水は純水であり、配合したゲル原料を作製されたゲル袋に注入し、排気後に加熱して封口し、2枚の強化ガラスまたは石英ガラスでゲル袋をプレスして平らにし、コンベアによりガラスでプレスしたゲル袋半製品を、紫外線の単位面積当たりの照射強度が50mJ/cm2〜5000mJ/cm2で、硬化時間が10秒である紫外線照射機に搬送して硬化させ、最後にコンベアにより紫外線区間を経過したゲルマットの初期製品を送出し、バリ取り後に検査包装した。
Example 3
30 kg of monomer, 2 kg of cross-linking agent, 2 kg of photoinitiator, 66 kg of water were added and 100 kg of gel raw material was blended. The monomers used were alkali metal acrylate, ester formed from methacrylic acid, acrylamide, methacrylamide, AMPS ( 2-acrylamido-2-methylpropanesulfonic acid) or a mixture of two or more, for example, a 5: 1: 2: 1 mixture of acrylamide: AMPS: sodium acrylate: methacrylamide. The used cross-linking agent is a compound having a plurality of non-conjugated double bonds, such as polyhydric alcohol (glycerin), N, N′-methylenebisacrylamide, for example, glycerin and N, N′-methylenebisacrylamide. The photo-initiator used is a commercially available diaryliodonium salt (US company GE) that is usually used, water is pure water, and the blended gel material is injected into the prepared gel bag. The gel bag semi-finished product heated and sealed after evacuation, pressed and flattened with two sheets of tempered glass or quartz glass, and pressed with glass by a conveyor has an irradiation intensity of 50 mJ / unit of ultraviolet light. in cm 2 ~5000mJ / cm 2, Geruma' the curing time and then cured by conveying the ultraviolet ray irradiation device is 10 seconds, it has elapsed ultraviolet interval by the last conveyor And of sending the initial product, it was tested packaging after deburring.
1 コンベア
2 紫外線照射ボックス
3 ガラス
4 ゲル原料が注入されたゲル袋
4 ゲル袋
5 ゲル
DESCRIPTION OF SYMBOLS 1
Claims (7)
モノマー5〜30%、架橋剤0.01〜2%、光開始剤0.001〜2%、残部の水からなることを特徴とする、請求項1記載のゲルマット。 The gel is, as a percentage, the following composition:
The gel mat according to claim 1, comprising 5 to 30% of a monomer, 0.01 to 2% of a crosslinking agent, 0.001 to 2% of a photoinitiator, and the balance of water.
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WO2012129968A1 (en) | 2012-10-04 |
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US20140010987A1 (en) | 2014-01-09 |
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