US20140010987A1 - Gel Mat and Its UV Solidification Production Method - Google Patents

Gel Mat and Its UV Solidification Production Method Download PDF

Info

Publication number
US20140010987A1
US20140010987A1 US13/636,130 US201213636130A US2014010987A1 US 20140010987 A1 US20140010987 A1 US 20140010987A1 US 201213636130 A US201213636130 A US 201213636130A US 2014010987 A1 US2014010987 A1 US 2014010987A1
Authority
US
United States
Prior art keywords
gel
foresaid
initiating agent
light
agent
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
Application number
US13/636,130
Inventor
Zhu Xuebing
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NEW CONCEPT DEVS GROUP Ltd
Original Assignee
NEW CONCEPT DEVS GROUP Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by NEW CONCEPT DEVS GROUP Ltd filed Critical NEW CONCEPT DEVS GROUP Ltd
Assigned to NEW CONCEPT DEVELOPMENTS GROUP LIMITED reassignment NEW CONCEPT DEVELOPMENTS GROUP LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: Zhu, Xuebing
Publication of US20140010987A1 publication Critical patent/US20140010987A1/en
Abandoned legal-status Critical Current

Links

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
    • A47C27/085—Fluid mattresses 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

Definitions

  • the utility model concerns a gel mat and its UV solidification production method.
  • the utility model aims at solving the above mentioned problems with the existing technology when producing gel mat, and providing a production method of gel mat and UV solidification.
  • the utility model concerns gel mat, comprising of gel pack, characterized ion that: the gel pack is filled with gel, and the foresaid gel is composed of monocase, cross-linking agent, light initiating agent and water solidified with UV light. It characterizes in that: the foresaid gel is composed of the following compositions at the following percentage:
  • the foresaid monocase is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid.
  • the foresaid cross-linking agent is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide.
  • the foresaid light initiating agent is a pyrolysis initiating agent or photosensitive initiating agent or cation initiating agent.
  • the outer layer of the gel pack is cotton cloth or Nylon cloth or terylene cloth
  • the inner layer is PVC film or TPU film or PE film or EVA film.
  • Production method of gel mat UB solidification characterizes in that: it is composed of 5 steps including making gel pack, filling, sealing, UV solidification, and package inspection. During UV solidification, perform certain pressure on to the gel pack filled and sealed, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat. UV radiation intensity per unit of area is 50 mJ/cm 2 -5000 mJ/cm 2 , and the solidification time is 10 seconds to 60 minutes. The semi-finished gel pack pressed ready by glass is sent to UV light area with the conveyor as primary finished product waiting for trimming, inspection and packaging. Advantages of this utility model include simple production technics, fast gel solidification and smooth gel mat produced.
  • FIG. 1 is an illustration of processing equipment of the utility model. 1 indicates the conveyor, 2 indicates the UV light radiation box, 3 indicates the glass and 4 indicates the gel pack filled with gel material;
  • FIG. 2 is a structure sectional illustration of the utility model. 4 indicates the gel pack and 5 indicates the gel.
  • the figure comprises of gel pack, characterized in that: the gel pack is filled with gel, and the foresaid gel is composed of monocase, cross-linking agent, light initiating agent and water solidified with UV light. It characterizes in that: the foresaid gel is composed of the following compositions at the following percentage:
  • the foresaid monocase is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid.
  • the foresaid cross-linking agent is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide.
  • the foresaid light initiating agent is a pyrolysis initiating agent or photosensitive initiating agent or cation initiating agent.
  • the outer layer of the gel pack is cotton cloth or Nylon cloth or terylene cloth
  • the inner layer is PVC film or TPU film or PE film or EVA film.
  • Production method of gel mat UB solidification characterizes in that: it is composed of 5 steps including making gel pack, filling, sealing, UV solidification, and package inspection. During UV solidification, perform certain pressure on to the gel pack filled and sealed, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat. UV radiation intensity per unit of area is 50 mJ/cm 2 -5000 mJ/cm 2 , and the solidification time is 10 seconds to 60 minutes. The semi-finished gel pack pressed ready by glass is sent to UV light area with the conveyor as primary finished product waiting for trimming, inspection and packaging.
  • the monocase used is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid, e.g. compound of sodium acrylate and AMPS at proportion of 3:1.
  • the cross-linking agent used is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide.
  • the light initiating agent used is benzophenone (Jiangyin More Chemical names it as light initiating agent BP), and the water is purified water.
  • the prepared ready gel material into the prepared gel pack, hot seal the pack after expelling air from it, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat, send the gel pack semi-finished product pressed with the glass on the conveyor to the UV radiation machine for solidification.
  • UV radiation intensity per unit of area is 50 mJ/cm 2 -5000 mJ/cm 2 , and the solidification time is 60 minutes.
  • the primary finished product of gel mat after passing the UV light area is sent out to wait for trimming, inspection and packaging.
  • the monocase used is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid, e.g. compound of sodium acrylate, acrylamide and AMPS at proportion of 3:1:1.
  • the cross-linking agent used is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N,N′-methylene diacrylamide.
  • the light initiating agent used is light initiating agent 184 sold in the market (Methanone, 1-hydroxycyclohexyl phenyl ketone, Jiangyin More Chemical), and the water is purified water.
  • the prepared ready gel material into the prepared gel pack, hot seal the pack after expelling air from it, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat, send the gel pack semi-finished product pressed with the glass on the conveyor to the UV radiation machine for solidification.
  • UV radiation intensity per unit of area is 50 mJ/cm 2 -5000 mJ/cm 2 , and the solidification time is 3 minutes.
  • the primary finished product of gel mat after passing the UV light area is sent out to wait for trimming, inspection and packaging.
  • the monocase used is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid, e.g. compound of acrylamide, AMPS, sodium acrylate, and methyl acrylamide at proportion of 5:1:2:1.
  • the cross-linking agent used is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide.
  • the light initiating agent used is diaryliodonium salt sold in the market (USA CE Company), and the water is purified water.
  • the prepared ready gel material into the prepared gel pack, hot seal the pack after expelling air from it, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat, send the gel pack semi-finished product pressed with the glass on the conveyor to the UV radiation machine for solidification.
  • UV radiation intensity per unit of area is 50 mJ/cm 2 -5000 mJ/cm 2 , and the solidification time is 10 seconds.
  • the primary finished product of gel mat after passing the UV light area is sent out to wait for trimming, inspection and packaging.

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)
  • Invalid Beds And Related Equipment (AREA)
  • Thermotherapy And Cooling Therapy Devices (AREA)
  • Mattresses And Other Support Structures For Chairs And Beds (AREA)
  • Polymerisation Methods In General (AREA)
  • Cosmetics (AREA)

Abstract

The utility model concerns a gel mat and its UV solidification production method, comprising of gel pack, characterized in that: the gel pack is filled with gel, and the foresaid gel is composed of monocase, cross-linking agent, light initiating agent and water solidified with UV light. It characterizes in that: the foresaid gel is composed of the following compositions at certain percentage: monocase, cross-linking agent, light imitating agent, and water. It also characterizes in that: the foresaid monocase is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid, characterized in that: the foresaid cross-linking agent is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide. It characterizes in that: the foresaid light initiating agent is a pyrolysis initiating agent or photosensitive initiating agent or cation initiating agent. Advantages of this utility model include simple production technics, fast gel solidification and smooth gel mat produced.

Description

    TECHNICAL FIELD
  • The utility model concerns a gel mat and its UV solidification production method.
  • BACKGROUND ART
  • For recent years, some cool mats (e.g. application No.: 200810063081.4) as gel mat were put into market. However, they are troubled with insufficient cool duration and unremarkable cool sense. In addition, during production of the products, surface of the product is with long “concave”; the content is easily spattered on to outer package material causing dirty for the surface of the product; in case of uncompleted air expelled from the pack during sealing, there will be plenty of “concaves” on surface of the product, and thus makes the product ugly by appearance; the production process needs thermal pressure, and therefore costs much energy; when the product is produced, it can not be packaged until cooled. Thus, it is with the shortcoming of complicated production process and large area needed for the factory.
  • Moreover, theses methods in production need long term for heating solidification, costs plenty of energy and achieves a low efficiency (e.g. application No.: 200810063081.4). Some of the methods cost less energy, but over 5 hours are required for solidification and thus seriously lowered production efficiency and operation; in addition, some gel mats formed with macromolecule cross-linking are troubled with serious problems like insufficient intensity, short lifespan of colloid and easily distortion caused, and insufficient solidification.
  • Contents of the Invention
  • This utility model aims at solving the above mentioned problems with the existing technology when producing gel mat, and providing a production method of gel mat and UV solidification. The utility model concerns gel mat, comprising of gel pack, characterized ion that: the gel pack is filled with gel, and the foresaid gel is composed of monocase, cross-linking agent, light initiating agent and water solidified with UV light. It characterizes in that: the foresaid gel is composed of the following compositions at the following percentage:
      • Monocase: 5-30%
      • Cross-linking agent: 0.01-2%
      • Light initiating agent: 0.001-2%
      • The remainder is water.
  • It characterizes in that: the foresaid monocase is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid. It characterizes in that: the foresaid cross-linking agent is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide. It characterizes in that: the foresaid light initiating agent is a pyrolysis initiating agent or photosensitive initiating agent or cation initiating agent. It characterizes in that: the outer layer of the gel pack is cotton cloth or Nylon cloth or terylene cloth, and the inner layer is PVC film or TPU film or PE film or EVA film. Production method of gel mat UB solidification characterizes in that: it is composed of 5 steps including making gel pack, filling, sealing, UV solidification, and package inspection. During UV solidification, perform certain pressure on to the gel pack filled and sealed, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat. UV radiation intensity per unit of area is 50 mJ/cm2-5000 mJ/cm2, and the solidification time is 10 seconds to 60 minutes. The semi-finished gel pack pressed ready by glass is sent to UV light area with the conveyor as primary finished product waiting for trimming, inspection and packaging. Advantages of this utility model include simple production technics, fast gel solidification and smooth gel mat produced.
  • DESCRIPTION OF FIGURES
  • FIG. 1 is an illustration of processing equipment of the utility model. 1 indicates the conveyor, 2 indicates the UV light radiation box, 3 indicates the glass and 4 indicates the gel pack filled with gel material;
  • FIG. 2 is a structure sectional illustration of the utility model. 4 indicates the gel pack and 5 indicates the gel.
  • MODE OF CARRYING OUT THE INVENTION
  • In the figure, it comprises of gel pack, characterized in that: the gel pack is filled with gel, and the foresaid gel is composed of monocase, cross-linking agent, light initiating agent and water solidified with UV light. It characterizes in that: the foresaid gel is composed of the following compositions at the following percentage:
      • Monocase: 5-30%
      • Cross-linking agent: 0.01-2%
      • Light initiating agent: 0.001-2%
      • The remainder is water.
  • It characterizes in that: the foresaid monocase is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid. It characterizes in that: the foresaid cross-linking agent is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide. It characterizes in that: the foresaid light initiating agent is a pyrolysis initiating agent or photosensitive initiating agent or cation initiating agent. It characterizes in that: the outer layer of the gel pack is cotton cloth or Nylon cloth or terylene cloth, and the inner layer is PVC film or TPU film or PE film or EVA film. Production method of gel mat UB solidification characterizes in that: it is composed of 5 steps including making gel pack, filling, sealing, UV solidification, and package inspection. During UV solidification, perform certain pressure on to the gel pack filled and sealed, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat. UV radiation intensity per unit of area is 50 mJ/cm2-5000 mJ/cm2, and the solidification time is 10 seconds to 60 minutes. The semi-finished gel pack pressed ready by glass is sent to UV light area with the conveyor as primary finished product waiting for trimming, inspection and packaging.
  • Embodiment 1
  • Take 5 Kg monocase, 0.01 Kg cross-linking agent, 0.001 Kg light initiating agent, 94.989 Kg water to form gel material at weight of 100 Kg. The monocase used is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid, e.g. compound of sodium acrylate and AMPS at proportion of 3:1. The cross-linking agent used is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide. Taking glycerol as an example, the light initiating agent used is benzophenone (Jiangyin More Chemical names it as light initiating agent BP), and the water is purified water. Fill the prepared ready gel material into the prepared gel pack, hot seal the pack after expelling air from it, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat, send the gel pack semi-finished product pressed with the glass on the conveyor to the UV radiation machine for solidification. UV radiation intensity per unit of area is 50 mJ/cm2-5000 mJ/cm2, and the solidification time is 60 minutes. The primary finished product of gel mat after passing the UV light area is sent out to wait for trimming, inspection and packaging.
  • Embodiment 2
  • Take 22 Kg monocase, 1 Kg cross-linking agent, 1 Kg light initiating agent, 76 Kg water to form gel material at weight of 100 Kg. The monocase used is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid, e.g. compound of sodium acrylate, acrylamide and AMPS at proportion of 3:1:1. The cross-linking agent used is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N,N′-methylene diacrylamide. Taking N, N′-methylene diacrylamide as an example, the light initiating agent used is light initiating agent 184 sold in the market (Methanone, 1-hydroxycyclohexyl phenyl ketone, Jiangyin More Chemical), and the water is purified water. Fill the prepared ready gel material into the prepared gel pack, hot seal the pack after expelling air from it, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat, send the gel pack semi-finished product pressed with the glass on the conveyor to the UV radiation machine for solidification. UV radiation intensity per unit of area is 50 mJ/cm2-5000 mJ/cm2, and the solidification time is 3 minutes. The primary finished product of gel mat after passing the UV light area is sent out to wait for trimming, inspection and packaging.
  • Embodiment 3
  • Take 30 Kg monocase, 2 Kg cross-linking agent, 2 Kg light initiating agent, 66 Kg water to form gel material at weight of 100 Kg. The monocase used is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid, e.g. compound of acrylamide, AMPS, sodium acrylate, and methyl acrylamide at proportion of 5:1:2:1. The cross-linking agent used is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide. Taking compound of glycerol and N, N′-methylene diacrylamide as an example, the light initiating agent used is diaryliodonium salt sold in the market (USA CE Company), and the water is purified water. Fill the prepared ready gel material into the prepared gel pack, hot seal the pack after expelling air from it, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat, send the gel pack semi-finished product pressed with the glass on the conveyor to the UV radiation machine for solidification. UV radiation intensity per unit of area is 50 mJ/cm2-5000 mJ/cm2, and the solidification time is 10 seconds. The primary finished product of gel mat after passing the UV light area is sent out to wait for trimming, inspection and packaging.

Claims (7)

1. A gel mat, comprising of gel pack, characterized in that: the gel pack is filled with gel, and the foresaid gel is composed of monocase, cross-linking agent, light initiating agent and water solidified with UV light.
2. The gel mat as set forth in claim 1, characterized in that: the foresaid gel is composed of the following compositions at the following percentage:
Monocase: 5-30%
Cross-linking agent: 0.01-2%
Light initiating agent: 0.001-2%
The remainder is water.
3. The gel mat as set forth in claim 1, characterized in that: the foresaid monocase is a composition with two or more compositions including ester, acrylamide, methyl acrylamide, AMPS (2-Acrylamide-2-methylpro panesulfonic acid) generated from acryl acid, alkali metallic salt, methacrylic acid;
4. The gel mat as set forth in claim 1, characterized in that: the foresaid cross-linking agent is a composition with more non conjugated double bonds, is polyhydric alcohols (Glycerol), N, N′-methylene diacrylamide;
5. The gel mat as set forth in claim 1, characterized in that: the foresaid light initiating agent is a pyrolysis initiating agent or photosensitive initiating agent or cation initiating agent;
6. The gel mat as set forth in claim 1, characterized in that: the outer layer of the gel pack is cotton cloth or Nylon cloth or terylene cloth, and the inner layer is PVC film or TPU film or PE film or EVA film;
7. Production method of gel mat UB solidification characterizes in that: it is composed of 5 steps including making gel pack, filling, sealing, UV solidification, and package inspection. During UV solidification, perform certain pressure on to the gel pack filled and sealed, nip two pieces of tempered glass or quartz glass at two sides of the gel pack to press the gel pack flat. UV radiation intensity per unit of area is 50 mJ/cm2-5000 mJ/cm2, and the solidification time is 10 seconds to 60 minutes. The semi-finished gel pack pressed ready by glass is sent to UV light area with the conveyor as primary finished product waiting for trimming, inspection and packaging.
US13/636,130 2011-03-30 2012-03-30 Gel Mat and Its UV Solidification Production Method Abandoned US20140010987A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2011100783012A CN102715751A (en) 2011-03-30 2011-03-30 Gel pad and UV-curving production method thereof
CN201110078301.2 2011-03-30
PCT/CN2012/000416 WO2012129968A1 (en) 2011-03-30 2012-03-30 Gel pad and method for producing same by ultraviolet light curing

Publications (1)

Publication Number Publication Date
US20140010987A1 true US20140010987A1 (en) 2014-01-09

Family

ID=46929404

Family Applications (1)

Application Number Title Priority Date Filing Date
US13/636,130 Abandoned US20140010987A1 (en) 2011-03-30 2012-03-30 Gel Mat and Its UV Solidification Production Method

Country Status (4)

Country Link
US (1) US20140010987A1 (en)
JP (1) JP5529197B2 (en)
CN (1) CN102715751A (en)
WO (1) WO2012129968A1 (en)

Families Citing this family (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103082734A (en) * 2012-12-31 2013-05-08 上海易舜冰袋有限公司 Production method of gel pad
EP3187938A1 (en) 2013-02-12 2017-07-05 CARBON3D, Inc. Method and apparatus for three-dimensional fabrication with feed through carrier
MX350841B (en) 2013-02-12 2017-09-18 Carbon3D Inc METHOD AND APPLIANCE FOR THREE-DIMENSIONAL MANUFACTURING.
WO2014192616A1 (en) * 2013-05-28 2014-12-04 シャープ株式会社 Heat storage member, manufacturing method of same, and storage container, refrigerator, packaging container, clothing, glass and pillow using said heat storage member
WO2015142546A1 (en) 2014-03-21 2015-09-24 Carbon3D, Inc. Method and apparatus for three-dimensional fabrication with gas injection through carrier
WO2015164234A1 (en) 2014-04-25 2015-10-29 Carbon3D, Inc. Continuous three dimensional fabrication from immiscible liquids
ES2711849T3 (en) 2014-06-20 2019-05-07 Carbon Inc Three-dimensional printing with reciprocal feed of polymerizable liquid
WO2015195920A1 (en) 2014-06-20 2015-12-23 Carbon3D, Inc. Three-dimensional printing method using increased light intensity and apparatus therefore
WO2015195909A1 (en) 2014-06-20 2015-12-23 Carbon3D, Inc. Three-dimensional printing using tiled light engines
AU2015280283B2 (en) 2014-06-23 2019-05-02 Carbon, Inc. Methods of producing three-dimensional objects from materials having multiple mechanisms of hardening
US11390062B2 (en) 2014-08-12 2022-07-19 Carbon, Inc. Three-dimensional printing with supported build plates
EP3240671B1 (en) 2014-12-31 2020-12-16 Carbon, Inc. Three-dimensional printing of objects with breathing orifices
US20160193786A1 (en) 2015-01-06 2016-07-07 Carbon3D, Inc. Three-dimensional printing with build plates having a rough or patterned surface and related methods
WO2016112090A1 (en) 2015-01-07 2016-07-14 Carbon3D, Inc. Microfluidic devices and methods of making the same
US20160200052A1 (en) 2015-01-13 2016-07-14 Carbon3D, Inc. Three-dimensional printing with build plates having surface topologies for increasing permeability and related methods
US20180133959A1 (en) 2015-01-30 2018-05-17 Carbon, Inc. Build plates for continuous liquid interface printing having permeable sheets and related methods, systems and devices
US11020898B2 (en) 2015-01-30 2021-06-01 Carbon, Inc. Build plates for continuous liquid interface printing having permeable base and adhesive for increasing permeability and related methods, systems and devices
WO2016126779A1 (en) 2015-02-05 2016-08-11 Carbon3D, Inc. Method of additive manufacturing by fabrication through multiple zones
WO2016133759A1 (en) 2015-02-20 2016-08-25 Carbon3D, Inc. Methods and apparatus for continuous liquid interface printing with electrochemically supported dead zone
WO2016140888A1 (en) 2015-03-05 2016-09-09 Carbon3D, Inc. Fabrication of three dimensional objects with variable slice thickness
WO2016140891A1 (en) 2015-03-05 2016-09-09 Carbon3D, Inc. Continuous liquid interface production with sequential patterned exposure
US10391711B2 (en) 2015-03-05 2019-08-27 Carbon, Inc. Fabrication of three dimensional objects with multiple operating modes
WO2016145050A1 (en) 2015-03-10 2016-09-15 Carbon3D, Inc. Microfluidic devices having flexible features and methods of making the same
WO2016145182A1 (en) 2015-03-12 2016-09-15 Carbon3D, Inc. Additive manufacturing using polymerization initiators or inhibitors having controlled migration
WO2016149151A1 (en) 2015-03-13 2016-09-22 Carbon3D, Inc. Three-dimensional printing with concurrent delivery of different polymerizable liquids
WO2016149097A1 (en) 2015-03-13 2016-09-22 Carbon3D, Inc. Three-dimensional printing with reduced pressure build plate unit
US10792856B2 (en) 2015-03-13 2020-10-06 Carbon, Inc. Three-dimensional printing with flexible build plates
US10800094B2 (en) 2015-09-14 2020-10-13 Carbon, Inc. Light-curable article of manufacture with portions of differing solubility
WO2017053783A1 (en) 2015-09-25 2017-03-30 Carbon3D, Inc. Build plate assemblies for continuous liquid interphase printing having lighting panels and related methods, systems and devices
WO2017059082A1 (en) 2015-09-30 2017-04-06 Carbon, Inc. Method and apparatus for producing three-dimensional objects
WO2017066584A1 (en) 2015-10-15 2017-04-20 Saint-Gobain Ceramics & Plastics, Inc. Method for forming a three dimensional body from a mixture with a high content of solid particles
US10647873B2 (en) 2015-10-30 2020-05-12 Carbon, Inc. Dual cure article of manufacture with portions of differing solubility
WO2017112521A1 (en) 2015-12-22 2017-06-29 Carbon, Inc. Production of flexible products by additive manufacturing with dual cure resins
EP3341792A1 (en) 2015-12-22 2018-07-04 Carbon, Inc. Dual precursor resin systems for additive manufacturing with dual cure resins
US10647054B2 (en) 2015-12-22 2020-05-12 Carbon, Inc. Accelerants for additive manufacturing with dual cure resins
WO2017112682A1 (en) 2015-12-22 2017-06-29 Carbon, Inc. Fabrication of compound products from multiple intermediates by additive manufacturing with dual cure resins
WO2017112571A1 (en) 2015-12-22 2017-06-29 Carbon, Inc. Dual cure additive manufacturing of rigid intermediates that generate semi-rigid, flexible, or elastic final products
WO2017120806A1 (en) 2016-01-13 2017-07-20 中国科学院福建物质结构研究所 3d printing apparatus and method
WO2017210298A1 (en) 2016-05-31 2017-12-07 Northwestern University Method for the fabrication of three-dimensional objects and apparatus for same
CN211105627U (en) 2016-07-01 2020-07-28 卡本有限公司 Build plate for three-dimensional printer, build plate assembly and apparatus for forming three-dimensional object from polymerizable liquid
US11135790B2 (en) 2016-11-21 2021-10-05 Carbon, Inc. Method of making three-dimensional object by delivering reactive component for subsequent cure
US10239255B2 (en) 2017-04-11 2019-03-26 Molecule Corp Fabrication of solid materials or films from a polymerizable liquid
US11283189B2 (en) 2017-05-02 2022-03-22 Rogers Corporation Connected dielectric resonator antenna array and method of making the same
US11135766B2 (en) 2017-06-29 2021-10-05 Carbon, Inc. Products containing nylon 6 produced by stereolithography and methods of making the same
DK3655465T3 (en) 2017-07-21 2024-10-21 Saint Gobain Performance Plastics Corp PROCEDURE FOR FORMING A THREE-DIMENSIONAL BODY
US11616302B2 (en) 2018-01-15 2023-03-28 Rogers Corporation Dielectric resonator antenna having first and second dielectric portions
WO2019164808A1 (en) 2018-02-20 2019-08-29 The Regents Of The University Of Michigan Polymerization photoinhibitor
US11552390B2 (en) 2018-09-11 2023-01-10 Rogers Corporation Dielectric resonator antenna system
TWI820237B (en) 2018-10-18 2023-11-01 美商羅傑斯公司 Polymer structure, its stereolithography method of manufacture, and electronic device comprising same
JP2022510892A (en) 2018-12-04 2022-01-28 ロジャーズ コーポレーション Dielectric electromagnetic structure and its manufacturing method
NL2022372B1 (en) 2018-12-17 2020-07-03 What The Future Venture Capital Wtfvc B V Process for producing a cured 3d product
CN109718002B (en) * 2018-12-28 2021-08-17 义乌市安航科技有限公司 Heating patch with slow-release health care function
CN118636467A (en) 2019-03-07 2024-09-13 西北大学 Method for forming a three-dimensional object and device for forming a three-dimensional object
KR20220016453A (en) 2019-04-09 2022-02-09 아줄 쓰리디, 인크. Methodologies for rapidly curing and coating parts produced by additive manufacturing
EP3942366B1 (en) 2019-05-30 2023-11-15 Rogers Corporation Photocurable compositions for stereolithography, stereolithography methods using the compositions, polymer components formed by the stereolithography methods, and a device including the polymer components
US11482790B2 (en) 2020-04-08 2022-10-25 Rogers Corporation Dielectric lens and electromagnetic device with same
DE112022005305T5 (en) 2021-11-04 2024-08-29 The Procter & Gamble Company WEB MATERIAL STRUCTURING TAPE, METHOD OF MANUFACTURING AND METHOD OF USING
GB2626904A (en) 2021-11-04 2024-08-07 Procter & Gamble Web material structuring belt, method for making structured web material and structured web material made by the method
DE112022005294T5 (en) 2021-11-04 2024-08-29 The Procter & Gamble Company WEB MATERIAL STRUCTURING TAPE, METHOD OF MANUFACTURING AND METHOD OF USING
GB2627655A (en) 2021-11-04 2024-08-28 Procter & Gamble Web material structuring belt, method for making structured web material and structured web material made by the method
CA3237079A1 (en) 2023-05-02 2025-06-17 The Procter & Gamble Company Web material structuring belt comprising a seam and method for making and using

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4206827A1 (en) * 1991-03-06 1992-09-10 Sanyo Chemical Ind Ltd Low-temp. gel-type insulating material - contains water-absorbent gel of insol., water-absorbent polymer, aq. gel of water-soluble polymer and opt. a hydrophilic alcohol
EP1245241A1 (en) * 2001-03-30 2002-10-02 The Procter & Gamble Company Polymerized hydrogel adhesives comprising low amounts of residual monomers
US20100009128A1 (en) * 2008-07-09 2010-01-14 HIRAKAWA CORPORATION & Litao FAN Gel mat and method for manufacturing the same
US20100261850A1 (en) * 2007-10-09 2010-10-14 Nippon Shokubai Co., Ltd. Surface treatment method for water-absorbent resin

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6161147A (en) * 1984-08-31 1986-03-28 Kuraray Co Ltd Photoresponsive material
CN1039609A (en) * 1988-07-15 1990-02-14 上海科技大学 The method of the dynamic synthetic water gelatinous material of UV-light
US5590430A (en) * 1993-10-15 1997-01-07 Sereboff; Joel L. Gel filled deformable cushion and composition contained therein
JP3513568B2 (en) * 1995-12-06 2004-03-31 日東電工株式会社 Oily gel molding and method for producing the same
DE19909382C2 (en) * 1999-03-04 2003-04-30 Multigestion Deutschland Gmbh Process for making a pillow with a textured surface and gel filling
JP2000325410A (en) * 1999-05-24 2000-11-28 Kohjin Co Ltd Mat
JP2003199650A (en) * 2002-11-29 2003-07-15 Sanyo Chem Ind Ltd Mat with water absorbent resin
CN1304441C (en) * 2005-09-30 2007-03-14 清华大学 Direct synthesis of temperate sensitive aquogel by ultraviolet radiant polymerization
CN1834111A (en) * 2006-03-10 2006-09-20 清华大学 Process of directly synthetizing pH sensitive aquagel polymerized by UV radiation
US20080263772A1 (en) * 2007-04-30 2008-10-30 Li-Ya Chiu Adjustable pad according user's weight
CN101113207B (en) * 2007-06-27 2011-05-18 中国科学技术大学 Preparation method of sol-gel ultraviolet/heat cross-linking of hybridized anion exchange membrane
WO2009076572A2 (en) * 2007-12-12 2009-06-18 3M Innovative Properties Company Methods of making an article and articles
JP2010002154A (en) * 2008-06-23 2010-01-07 Ooshin Mlp:Kk Heating device
CN201341656Y (en) * 2008-11-25 2009-11-11 伦志柱 Cushion bag with hydrogel sealed therein
JP2010201149A (en) * 2009-02-09 2010-09-16 Nomura Trading Co Ltd Cold insulating bedding
CN101526632B (en) * 2009-03-10 2011-08-24 海昌隐形眼镜有限公司 Hydrogel contact glass material and preparation method thereof
CN201645944U (en) * 2010-04-19 2010-11-24 上海艾可杰生物高分子材料有限公司 Punching hydrogel pad

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4206827A1 (en) * 1991-03-06 1992-09-10 Sanyo Chemical Ind Ltd Low-temp. gel-type insulating material - contains water-absorbent gel of insol., water-absorbent polymer, aq. gel of water-soluble polymer and opt. a hydrophilic alcohol
EP1245241A1 (en) * 2001-03-30 2002-10-02 The Procter & Gamble Company Polymerized hydrogel adhesives comprising low amounts of residual monomers
US20100261850A1 (en) * 2007-10-09 2010-10-14 Nippon Shokubai Co., Ltd. Surface treatment method for water-absorbent resin
US20100009128A1 (en) * 2008-07-09 2010-01-14 HIRAKAWA CORPORATION & Litao FAN Gel mat and method for manufacturing the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Machine Translation of DE 4,206,827 C2. Obtained using Google machine translation service on 9 January 2014. *

Also Published As

Publication number Publication date
JP2012210408A (en) 2012-11-01
CN102715751A (en) 2012-10-10
WO2012129968A1 (en) 2012-10-04
JP5529197B2 (en) 2014-06-25

Similar Documents

Publication Publication Date Title
CN102715751A (en) Gel pad and UV-curving production method thereof
CN102963104B (en) Preparation method of back-sealing vacuum insulation panel
CN105751673A (en) LED encapsulation printer and LED encapsulation method
CN114774023B (en) EPE photovoltaic adhesive film, preparation method thereof and photovoltaic module
ATE541699T1 (en) STACK SEAL SHRINK FILM
JPWO2001061763A1 (en) Solar cell sealing film and method for manufacturing solar cell
CN104497899A (en) High-reflectivity photovoltaic module packaging film and application thereof
WO2013044179A3 (en) Ultraviolet device encapsulant
CN105914389B (en) A kind of laser accurate welding method of Soft Roll aluminum hull battery core edge sealing
CN104617170A (en) Solar spectrum conversion resin and preparation and application methods thereof
CN205573205U (en) High reflecting rate solar cell encapsulation glued membrane structure and dual glass assembly
CN105907046A (en) SMC (sheet molding compound) material and preparation method thereof
CN103555217B (en) EVA (ethylene-vinyl acetate) locating adhesive tape for crystalline silicon solar cell module
CN103367498B (en) The two glass assembly of a kind of solar energy and method for packing thereof
CN102760792A (en) Dry method packaging process of solar cell panel with rigid back plate
CN205366152U (en) A seal membrane machine for a cosmetics packaging box membrane
CN202025779U (en) Anti-sticking structure for solar module
CN103884118A (en) Adhesive package structure of flat-plate solar heat collector
CN204189905U (en) The top sealing mechanism of battery first top side sealer
CN204323733U (en) The package mechanism of electrode slice apparatus for production line
CN204189904U (en) The both sides sealing mechanism of battery first top side sealer
CN210942398U (en) Even quality board plastic film packing plant
CN205248293U (en) Shovel rubber cutter who uses during production solar PV modules
CN201638826U (en) A kind of solar cell adhesive film
CN204548649U (en) A kind of closing device of wrapping machine

Legal Events

Date Code Title Description
AS Assignment

Owner name: NEW CONCEPT DEVELOPMENTS GROUP LIMITED, HONG KONG

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ZHU, XUEBING;REEL/FRAME:028992/0399

Effective date: 20120731

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION