CN105878054A - LED-UV phototherapy glue scrubbing-free sealing layer glue and preparation method thereof - Google Patents

LED-UV phototherapy glue scrubbing-free sealing layer glue and preparation method thereof Download PDF

Info

Publication number
CN105878054A
CN105878054A CN201610214824.8A CN201610214824A CN105878054A CN 105878054 A CN105878054 A CN 105878054A CN 201610214824 A CN201610214824 A CN 201610214824A CN 105878054 A CN105878054 A CN 105878054A
Authority
CN
China
Prior art keywords
glue
led
phototherapy
exempts
sealing glue
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
Application number
CN201610214824.8A
Other languages
Chinese (zh)
Other versions
CN105878054B (en
Inventor
徐钦昌
朱鑫
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.)
UV TECH MATERIAL Co Ltd
Original Assignee
UV TECH MATERIAL Co 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 UV TECH MATERIAL Co Ltd filed Critical UV TECH MATERIAL Co Ltd
Priority to CN201610214824.8A priority Critical patent/CN105878054B/en
Publication of CN105878054A publication Critical patent/CN105878054A/en
Application granted granted Critical
Publication of CN105878054B publication Critical patent/CN105878054B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/87Polyurethanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/347Phenols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/415Aminophenols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/418Amines containing nitro groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4926Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4986Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with sulfur as the only hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/86Polyethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q3/00Manicure or pedicure preparations
    • A61Q3/02Nail coatings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/42Colour properties
    • A61K2800/43Pigments; Dyes
    • A61K2800/432Direct dyes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/42Colour properties
    • A61K2800/43Pigments; Dyes
    • A61K2800/434Luminescent, Fluorescent; Optical brighteners; Photosensitizers

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Sealing Material Composition (AREA)
  • Radiation-Therapy Devices (AREA)

Abstract

The invention discloses LED-UV phototherapy glue scrubbing-free sealing layer glue. The LED-UV phototherapy glue scrubbing-free sealing layer glue is prepared from, by weight concentration, 7-90% of oligomer, 7-90% of active monomers, 1-10% of photoinitiator, 1-10% of a mercaptan compound and 0.1-1% of stabilizer. The invention further discloses a preparation method of the LED-UV phototherapy glue scrubbing-free sealing layer glue. The scrubbing-free sealing layer glue can basically overcome the oxygen inhibition phenomenon, has a very high curing reaction rate and can be completely cured under an LED-UV weak light source, the situations that floating glue exists and the surface is not dry do not exist, and the curing time is shortened to about 60 s from general 120 s. Therefore, in the nail beautifying process, the scrubbing process is omitted, the nail beautifying process becomes simple, and manpower, material resources and time cost are saved.

Description

LED-UV phototherapy glue exempts to clean sealing glue and preparation method thereof
Technical field
The invention belongs to material chemistry technical field, particularly relate to LED-UV phototherapy glue exempt from clean sealing glue and Its preparation method.
Background technology
Phototherapy glue, also known as UV nail polish glue, belongs to the one of nial polish in color make-up, is coated in nail surface, warp UV light solidify to form thin film after irradiating, lucuriant in design, gloss is full so that the great aesthetic feeling of fingernail, deep by wide The welcome of big women and liking.
At present, on market nial polish mainly have water-based nail polish, nitro nial polish, UV phototherapy glue this in three, To have adhesive force good with other two kinds of nial polishs are compared for UV phototherapy glue, and the retention time is long, glossiness advantages of higher. The main flow having become nail salon uses product.
Current UV phototherapy glue is the formula for the design of UV mercury lamp light source, along with the rise of LED, LED-UV light source the most progressively substitutes UV mercury lamp light source, and future will become main flow, because of the light for solidification The spectral characteristic in source changes, and current UV phototherapy glue formula is badly in need of improvement.
Now, the phototherapy glue used on the market is three step glue: primer, color glue, sealing glue, the most in due order Sequence is respectively coated with and solidifies.Nail lamp is mainly with CCFL+LED as light source, and optical source wavelength peak value is 250nm、395nm.Nail lamp power is generally 12-36W.
Current UV phototherapy glue product existing defects need improvement, including length hardening time, exist floating glue, Need cleaning.The use of phototherapy glue and solidification process be exposed in air ambient according to radical polymerization principle Carrying out, the oxygen molecule in air has very important inhibition to radical polymerization, especially low Under the low light level of power LED-UV lamp, oxygen inhibition phenomenon is particularly evident.
Each layer (primer, face glue, color glue) of present three step phototherapy glue is solid under nail lamp after having coated The change time is required to more than 120s, and top layer still remains one layer of floating glue the most completely crued, it is impossible to surface drying. Need to continue to be coated with overlapping colours glue after solidifying due to primer, need after color adhesive curing to continue coating sealing glue, so this The floating glue of two-layer can need not process, and it can be handed over next step color glue dough-making powder glue being coated on face Connection curing reaction, but the floating glue of residual after nail lamp irradiates solidification on last sealing glue then must be used Cotton or cotton swab are stained with ethanol by its scrub.3rd step sealing glue is called to clean sealing in the industry, uses this Plant and clean sealing so that the slightly aobvious complexity of manicure technique, human and material resources and time cost increased.
Summary of the invention
The weak point that it is an object of the invention to overcome prior art to exist and provide a kind of LED-UV light Treat glue exempt from clean sealing glue, the present invention exempt from clean sealing glue can substantially overcome oxygen inhibition phenomenon, have very High curing reaction speed, can realize being fully cured under the such weak light source of LED-UV, not there are The situation of floating glue, not surface drying, and also shortened to about 60s by general 120s hardening time.Therefore exist Eliminate scouring process during manicure so that manicure technique becomes simple, saved human and material resources and time Between cost.
The technical solution used in the present invention is: a kind of LED-UV phototherapy glue exempts to clean sealing glue, comprises following The raw material of weight percent concentration: oligomer 7~90%, activated monomer 7~90%, light trigger 1~10%, Sulfur alcohol compound 1~10%, stabilizer 0.1~1%.
As the further improvement to technique scheme, described LED-UV phototherapy glue exempts to clean sealing glue, Comprise the raw material of following weight percent concentration: oligomer 45~55%, activated monomer 30~40%, light-initiated Agent 6~8%, sulfur alcohol compound 6.5~8.5%, stabilizer 0.4~0.6%.Weight percent when described raw material Specific concentration within the above range time, prepared LED-UV phototherapy glue exempt from clean sealing glue curing reaction speed Higher, hardening time is shorter.
As the further improvement to technique scheme, described oligomer is unsaturated polyester (UP), propylene oxide In acid esters, urethane acrylate, polyether acrylate, polyester acrylate, pure acrylic resin extremely Few one.
As the further improvement to technique scheme, described activated monomer selected from Monofunctional monomers and/or Bifunctional monomer.
As the further improvement to technique scheme, described Monofunctional monomers is acryloyl morpholine (ACMO), vinylacetate (VA), Isooctyl acrylate monomer (EHA), isobornyl acrylate (IBOA), In isobornyl methacrylate (IBOMA), crylic acid hydroxy ester, methacrylic acid hydroxyl ester at least A kind of.Described crylic acid hydroxy ester is preferably Hydroxyethyl Acrylate (HEA) and/or hydroxypropyl acrylate (HPA);Described methacrylic acid hydroxyl ester is preferably hydroxyethyl methacrylate (HEMA) and/or first Base hydroxypropyl acrylate (HPMA).
As the further improvement to technique scheme, described bifunctional monomer is 1,6-hexanediol two propylene Acid esters (HDDA), 1,4 butanediol diacrylate (BDDA), tri (propylene glycol) diacrylate (TPGDA), neopentylglycol dimethacrylate (NPGDMA), ethylene glycol dimethacrylate (EGDMA) at least one in.
The ultraviolet light of 250nm and 395nm wavelength is had response to absorb by described light trigger, causes photopolymerization Reaction.As the further improvement to technique scheme, described light trigger is 1-hydroxycyclohexylphenyl Ketone (184), 2-hydroxy-2-methyl-1-phenyl-1-acetone (1173), 2,4,6-trimethylbenzoyl-hexichol At least one in base phosphine oxide (TPO), 2-isopropyl thioxanthone (ITX).Light trigger can absorb purple Outer heat input, produces free radical, then causes coating oligomer and monomer to realize polymerization, crosslinking, make system hand over It is unified into film.
As the further improvement to technique scheme, described sulfur alcohol compound is ethylene glycol bisthioglycolate (3-sulfydryl Propionic ester) (GDMP), 1,4-butanediol two (3-thiopropionate) (BDMP), trimethylolpropane tris In (3-thiopropionate) (TMPMP), tetramethylolmethane four (3-thiopropionate) (PETMP) at least A kind of.
As the further improvement to technique scheme, described stabilizer be MEHQ (MEHQ), P-tert-Butylcatechol (TBC), p-methyl phenol, para-aminophenol, paranitrophenol, the tert-butyl group pair Hydroxyanisol (BHA), 2,6 di tert butyl 4 methyl phenol (BHT), three (2,4-DI-tert-butylphenol compounds) Phosphite ester (168), three (N-nitroso-group-N-Phenylhydroxylamine) aluminium salt (510), NO free radical piperidine alcohols (701) In at least one.
The LED-UV phototherapy glue of the present invention exempt from clean sealing glue by formula add sulfur alcohol compound and Stabilizer improves curing efficiency and overcomes oxygen inhibition phenomenon.
Specifically, the present invention is to add the thio-alcohol containing sulfydryl (-SH) in radically curing system Compound (namely sulfhydryl compound), so in radical polymerization process, in the presence of having oxygen, alkyl is certainly Being combined with oxygen atom by base, form peroxy radical, newly-generated peroxy radical again can be by capturing mercaptan The hydrogen atom of upper sulfydryl produces sulfydryl free radical, and polyreaction is again to carry out, and the existence of such oxygen is the most not Can cause the generation of oxygen inhibition phenomenon, very big due to the activity of sulfydryl free radical on the contrary, the speed of polymerization has The biggest raising.Then high due to sulfur alcohol compound activity, can dissociate sulfydryl free radical, is not having Ultraviolet light also can slowly occur dark reaction under irradiating, therefore to improve the storage stability of product, the present invention In system, add stabilizer, neutralize free sulfydryl free radical out, the generation of suppression dark reaction.
Scouring sealing glue of exempting from of the present invention can overcome oxygen inhibition existing under LED-UV nail lamp weak light source As, eliminate the phenomenon of the not dry viscous hands in top layer, technique and the step wiping floating glue can be exempted during manicure.
Scouring sealing glue of exempting from of the present invention can realize in 30-60S under LED-UV nail lamp is irradiated All solidstate, is greatly shortened the hardening time compared to existing frequently-used sealing glue 90-120S.
Present invention also offers described LED-UV phototherapy glue exempt from clean sealing glue preparation method, including with Lower step:
(1) by described oligomer, activated monomer, light trigger, sulfur alcohol compound, stabilizer mixing;
(2) at normal temperatures and pressures, the raw material mixed is stirred dispersion so that light trigger is the most molten Solving, each component is fully dispersed;
(3) standing sloughs bubble or vacuum sloughs bubble.
As the further improvement to technique scheme, carry out under conditions of rotating speed is 800~1500rpm Dispersed with stirring.
Relative to prior art, the invention have the benefit that
The LED-UV phototherapy glue of the present invention is exempted to clean sealing glue and is passed through can substantially overcome oxygen inhibition phenomenon, tool There is the highest curing reaction speed, can realize being fully cured under the such weak light source of LED-UV, not deposit There iing the situation of floating glue, not surface drying, and hardening time is also being shortened to about 60s by general 120s.Cause This eliminates scouring process during manicure so that manicure technique becomes simple, has saved human and material resources And time cost.Thus the property easy to use of existing product can be improved, provide more preferable experience for client.
The preparation method that the LED-UV phototherapy glue of the present invention exempts to clean sealing glue is simple, convenient.
Detailed description of the invention
For better illustrating the object, technical solutions and advantages of the present invention, below in conjunction with specific embodiment pair The present invention is described further.
Embodiment 1
Urethane acrylate (Sartomer 996), the epoxy acrylate (sand of 10wt% according to 45wt% Many agates E151), the acryloyl morpholine (ACMO, Japanese emerging people) of 10wt%, the 1,6-HD of 20wt% Diacrylate (HDDA, Changxing EM221), the 2,4,6-trimethylbenzoy-dipheny oxidation of 6wt% Phosphine (TPO, long day green wood), tetramethylolmethane four (3-thiopropionate) (PETMP tri-well of 8.5wt% Learn), three (N-nitroso-group-N-Phenylhydroxylamine) aluminium salt of 0.5wt% (510, English profit science and technology) mixed material feeding, often Under the conditions of normal temperature and pressure, stir with the speed of 1000rpm in blender, make light trigger fully dissolve and respectively Component is fully dispersed, then stand slough bubble, just obtained clarification bright exempt from clean sealing glue.
Embodiment 2
Urethane acrylate (Changxing DR-U120), the polyester acrylate of 20wt% according to 30wt% The hydroxyethyl methacrylate (HEMA, Mitsubishi) of (Changxing 6355), 35wt%, the 1-of 5wt% Hydroxycyclohexyl phenyl ketone (184, long day green wood), the 2 of 3wt%, 4,6-trimethylbenzoy-dipheny Phosphine oxide (TPO, long day green wood), 3wt% trimethylolpropane tris (3-thiopropionate) (TMPMP, Essence Dehua learn), the tetramethylolmethane four (3-thiopropionate) (PETMP Mitsui Chemicals) of 3.5wt%, 0.2wt% Three (N-nitroso-group-N-Phenylhydroxylamine) aluminium salt (510, English profit science and technology), the 2,6-di-t-butyl-4-of 0.3wt% Methylphenol (BHT, peaceful Kang Huagong) mixed material feeding, under normal temperature and pressure conditions, with 1200rpm in blender Speed stirring, make light trigger fully dissolve fully dispersed with each component, then stand slough bubble, just Obtained clarification bright exempt from clean sealing glue.
Embodiment 3
Urethane acrylate (Changxing DR-U240), the epoxy acrylate of 15wt% according to 30wt% (Sartomer E151), 10wt% pure acrylic resin (Changxing 6530B-4O), the acryloyl of 10wt% Quinoline (ACMO, Japanese emerging people), the hydroxyethyl methacrylate (HEMA, Mitsubishi) of 20wt%, 2wt% 1-hydroxycyclohexyl phenyl ketone (184, long day green wood), the 2 of 6wt%, 4,6-trimethylbenzoyls-two Phenyl phosphine oxide (TPO, long day green wood), 2wt% tetramethylolmethane four (3-thiopropionate) (PETMP, Mitsui Chemicals), the BDO two (3-thiopropionate) of 4.5wt% (BDMP, essence Dehua is learned), 0.1wt% P-methyl phenol, the para-aminophenol of 0.2wt%, three (2,4-DI-tert-butylphenol compounds) phosphite ester of 0.2wt% Mixed material feeding, under normal temperature and pressure conditions, in blender, the speed with 800rpm stirs, and makes light trigger fill Dividing dissolving and each component fully dispersed, then stand and slough bubble, the scouring of exempting from just having obtained clarification bright is sealed Layer glue.
Embodiment 4
Different pungent according to the polyether acrylate of 7wt%, 35wt% vinylacetate (VA), 25wt% acrylic acid Ester (EHA), 30wt%1,4-butanediol diacrylate (BDDA), 1.9wt%2-hydroxy-2-methyl-1-benzene Base-1-acetone (1173), 1wt% ethylene glycol bisthioglycolate (3-thiopropionate) (GDMP), 0.1wt% are to hydroxyl Methyl phenyl ethers anisole (MEHQ), mixed material feeding, under normal temperature and pressure conditions, with the speed of 800rpm in blender Stirring, makes light trigger fully dissolve fully dispersed with each component, then stands and sloughs bubble, just obtains Clarify bright exempting from and clean sealing glue.
Embodiment 5
According to 25wt% epoxy acrylate, 40wt% urethane acrylate, 25wt% polyester acrylate, 7wt% neopentylglycol dimethacrylate (NPGDMA), 1wt%2-isopropyl thioxanthone (ITX), 1.7wt% trimethylolpropane tris (3-thiopropionate) (TMPMP), 0.3wt% p-tert-Butylcatechol (TBC) mixed material feeding, under normal temperature and pressure conditions, in blender, the speed with 1000rpm stirs, and makes Light trigger fully dissolves fully dispersed with each component, then stands and sloughs bubble, has just obtained clarification bright Exempt from clean sealing glue.
Embodiment 6
According to 25wt% epoxy acrylate, 20wt% urethane acrylate, 20wt% isobornyl methyl-prop Olefin(e) acid ester (IBOMA), 20wt% hydroxypropyl acrylate (HPA), 8wt%2,4,6-trimethylbenzoyl Base-diphenyl phosphine oxide (TPO), wt% ethylene glycol bisthioglycolate (3-thiopropionate) (GDMP), wt%1,4- Butanediol two (3-thiopropionate) (BDMP), paranitrophenol, tert-butyl group MEHQ (BHA), NO free radical piperidine alcohols (701) mixed material feeding, under normal temperature and pressure conditions, with 1500rpm in blender Speed stirring, make light trigger fully dissolve fully dispersed with each component, then stand slough bubble, just Obtained clarification bright exempt from clean sealing glue.
Exempting from the LED-UV phototherapy glue of the present invention cleans sealing can be under conventional nail lamp be irradiated Being fully cured in 30-60S, glue is not floated on top layer, exempts to clean, is easy to use quick, time saving and energy saving.
Last institute is it should be noted that, above example is only in order to illustrate technical scheme rather than to this The restriction of invention protection domain, although the present invention being explained in detail with reference to preferred embodiment, this area It is to be appreciated by one skilled in the art that technical scheme can be modified or equivalent, and Spirit and scope without departing from technical solution of the present invention.

Claims (10)

1. a LED-UV phototherapy glue exempts to clean sealing glue, it is characterised in that: comprise following percentage by weight The raw material of concentration: oligomer 7~90%, activated monomer 7~90%, light trigger 1~10%, thio-alcohol Compound 1~10%, stabilizer 0.1~1%.
LED-UV phototherapy glue the most according to claim 1 exempts to clean sealing glue, it is characterised in that: institute State oligomer to be unsaturated polyester (UP), epoxy acrylate, urethane acrylate, polyether acrylate, gather At least one in ester acrylate, pure acrylic resin.
LED-UV phototherapy glue the most according to claim 1 exempts to clean sealing glue, it is characterised in that: institute State activated monomer selected from Monofunctional monomers and/or bifunctional monomer.
LED-UV phototherapy glue the most according to claim 3 exempts to clean sealing glue, it is characterised in that: institute State Monofunctional monomers for acryloyl morpholine, vinylacetate, Isooctyl acrylate monomer, isobornyl acrylate, At least one in isobornyl methacrylate, crylic acid hydroxy ester, methacrylic acid hydroxyl ester.
LED-UV phototherapy glue the most according to claim 3 exempts to clean sealing glue, it is characterised in that: institute State bifunctional monomer be 1,6 hexanediol diacrylate, 1,4 butanediol diacrylate, two contractings 3 the third two In alcohol diacrylate, neopentylglycol dimethacrylate, ethylene glycol dimethacrylate at least one Kind.
LED-UV phototherapy glue the most according to claim 1 exempts to clean sealing glue, it is characterised in that: institute Stating light trigger is 1-hydroxycyclohexyl phenyl ketone, 2-hydroxy-2-methyl-1-phenyl-1-acetone, 2,4,6-front three At least one in base benzoyl-diphenyl phosphine oxide, 2-isopropyl thioxanthone.
LED-UV phototherapy glue the most according to claim 1 exempts to clean sealing glue, it is characterised in that: institute State sulfur alcohol compound be ethylene glycol bisthioglycolate (3-thiopropionate), 1,4-butanediol two (3-thiopropionate), At least one in trimethylolpropane tris (3-thiopropionate), tetramethylolmethane four (3-thiopropionate).
LED-UV phototherapy glue the most according to claim 1 exempts to clean sealing glue, it is characterised in that: institute Stating stabilizer is MEHQ, p-tert-Butylcatechol, p-methyl phenol, para-aminophenol, right Nitrophenol, tert-butyl group MEHQ, 2,6 di tert butyl 4 methyl phenol, three (2,4-di-tert-butyls Phenol) phosphite ester, three (N-nitroso-group-N-Phenylhydroxylamine) aluminium salt, at least one in NO free radical piperidine alcohols.
9. exempt to clean the preparation of sealing glue according to the LED-UV phototherapy glue according to any one of claim 1~8 Method, it is characterised in that: comprise the following steps:
(1) by described oligomer, activated monomer, light trigger, sulfur alcohol compound, stabilizer mixing;
(2) at normal temperatures and pressures, the raw material mixed is stirred dispersion so that light trigger is the most molten Solving, each component is fully dispersed;
(3) standing sloughs bubble or vacuum sloughs bubble.
LED-UV phototherapy glue the most according to claim 9 exempts to clean the preparation method of sealing glue, its It is characterised by: under conditions of rotating speed is 800~1500rpm, be stirred dispersion.
CN201610214824.8A 2016-04-07 2016-04-07 LED-UV phototherapy glue exempts to clean sealing glue and preparation method thereof Active CN105878054B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610214824.8A CN105878054B (en) 2016-04-07 2016-04-07 LED-UV phototherapy glue exempts to clean sealing glue and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610214824.8A CN105878054B (en) 2016-04-07 2016-04-07 LED-UV phototherapy glue exempts to clean sealing glue and preparation method thereof

Publications (2)

Publication Number Publication Date
CN105878054A true CN105878054A (en) 2016-08-24
CN105878054B CN105878054B (en) 2018-11-16

Family

ID=57013520

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610214824.8A Active CN105878054B (en) 2016-04-07 2016-04-07 LED-UV phototherapy glue exempts to clean sealing glue and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105878054B (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107987581A (en) * 2018-01-03 2018-05-04 洛阳科迪艺思树脂有限公司 A kind of disposable sealing of UV-LED nails and preparation method thereof
CN108477809A (en) * 2018-05-31 2018-09-04 北京云绘智能科技有限公司 A kind of intelligence nail art device and manicure method
CN108611042A (en) * 2018-03-22 2018-10-02 深圳市姿彩科技有限公司 LED solidification drop glue
CN109010129A (en) * 2018-06-29 2018-12-18 广州杰奥斯精细化工有限公司 A kind of wearability it is good and can self-healing UV nail polish sealing and preparation method thereof
CN110917068A (en) * 2019-12-05 2020-03-27 山东益丰生化环保股份有限公司 UV-cured environment-friendly nail polish and preparation method thereof
CN111035575A (en) * 2019-12-16 2020-04-21 山东益丰生化环保股份有限公司 Uv-cured modified thiol resin nail polish and preparation method thereof
CN111607332A (en) * 2020-06-18 2020-09-01 上海固柯胶带科技有限公司 Rubber layer composition and protective film
WO2021007658A1 (en) * 2019-07-12 2021-01-21 Mondofix Inc. Thiol-based adhesive formulations for repairing windshields
CN113304070A (en) * 2021-06-16 2021-08-27 广州蓝之天化工科技发展有限公司 High-gloss low-yellowing wash-free sealing layer and preparation method thereof
CN113398005A (en) * 2021-05-13 2021-09-17 广州市鸿耀化工有限公司 Velvet nail oil glue seal layer and preparation method thereof
WO2022012694A1 (en) * 2020-07-17 2022-01-20 Guangdong Huarun Paints Co., Ltd. Uv-led curable and yellowing resistant coating composition
CN116376494A (en) * 2021-12-23 2023-07-04 武汉宜田科技发展有限公司 Medium-low temperature water boiling glue suitable for cutting large-size silicon wafer

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1526740A (en) * 2003-03-03 2004-09-08 珠海东诚化工有限公司 Photoinitiator composition capable of initiating via visible light and its use
CN101928541A (en) * 2010-05-19 2010-12-29 江苏和成化学材料有限公司 UV curable adhesive
CN102250309A (en) * 2011-06-16 2011-11-23 新丰见微化工实业有限公司 Flame-retarding ultraviolet curing aqueous polyurethane coating and preparation method thereof
CN105384906A (en) * 2015-12-22 2016-03-09 北京天山新材料技术有限公司 Photocuring prepolymer tackiness agent and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1526740A (en) * 2003-03-03 2004-09-08 珠海东诚化工有限公司 Photoinitiator composition capable of initiating via visible light and its use
CN101928541A (en) * 2010-05-19 2010-12-29 江苏和成化学材料有限公司 UV curable adhesive
CN102250309A (en) * 2011-06-16 2011-11-23 新丰见微化工实业有限公司 Flame-retarding ultraviolet curing aqueous polyurethane coating and preparation method thereof
CN105384906A (en) * 2015-12-22 2016-03-09 北京天山新材料技术有限公司 Photocuring prepolymer tackiness agent and preparation method thereof

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107987581A (en) * 2018-01-03 2018-05-04 洛阳科迪艺思树脂有限公司 A kind of disposable sealing of UV-LED nails and preparation method thereof
CN108611042A (en) * 2018-03-22 2018-10-02 深圳市姿彩科技有限公司 LED solidification drop glue
CN108477809B (en) * 2018-05-31 2024-02-27 北京云绘智能科技有限公司 Intelligent nail beautifying device and nail beautifying method
CN108477809A (en) * 2018-05-31 2018-09-04 北京云绘智能科技有限公司 A kind of intelligence nail art device and manicure method
CN109010129A (en) * 2018-06-29 2018-12-18 广州杰奥斯精细化工有限公司 A kind of wearability it is good and can self-healing UV nail polish sealing and preparation method thereof
WO2021007658A1 (en) * 2019-07-12 2021-01-21 Mondofix Inc. Thiol-based adhesive formulations for repairing windshields
CN110917068A (en) * 2019-12-05 2020-03-27 山东益丰生化环保股份有限公司 UV-cured environment-friendly nail polish and preparation method thereof
CN111035575A (en) * 2019-12-16 2020-04-21 山东益丰生化环保股份有限公司 Uv-cured modified thiol resin nail polish and preparation method thereof
CN111607332A (en) * 2020-06-18 2020-09-01 上海固柯胶带科技有限公司 Rubber layer composition and protective film
WO2022012694A1 (en) * 2020-07-17 2022-01-20 Guangdong Huarun Paints Co., Ltd. Uv-led curable and yellowing resistant coating composition
CN113398005A (en) * 2021-05-13 2021-09-17 广州市鸿耀化工有限公司 Velvet nail oil glue seal layer and preparation method thereof
CN113304070A (en) * 2021-06-16 2021-08-27 广州蓝之天化工科技发展有限公司 High-gloss low-yellowing wash-free sealing layer and preparation method thereof
CN116376494A (en) * 2021-12-23 2023-07-04 武汉宜田科技发展有限公司 Medium-low temperature water boiling glue suitable for cutting large-size silicon wafer

Also Published As

Publication number Publication date
CN105878054B (en) 2018-11-16

Similar Documents

Publication Publication Date Title
CN105878054A (en) LED-UV phototherapy glue scrubbing-free sealing layer glue and preparation method thereof
EP2782552B1 (en) Nail polish
CN102648222B (en) Removable color layer for artificial nail coatings and methods therefore
TWI595890B (en) Photo-curing nailgel composition
CN102639578B (en) Removable protective topcoat for artificial nail coatings and methods therefore
JP5475067B2 (en) Artificial nail material composition, method for curing artificial nail material composition, method for producing artificial nail, and artificial nail
CN105062405A (en) LED photocuring non-solvent type photosensitive transfer printing adhesive for cover plate glass substrate and preparation method thereof
WO2011071029A1 (en) Curable resin composition for covering a fingernail or artificial fingernail
EP3124509A1 (en) Fast light curing cyanoacrylate compositions
TWI717649B (en) Curable compositions containing thiol compounds
CN103242742B (en) A kind of waterborne radiation curable coating for coiled material PVC floor and preparation method thereof
KR101508734B1 (en) Uv-curable manicure to be changed color by light and temperature
CN102146272A (en) Radiation curing sealant for packaging eyeglass nameplate or ornament
JP2015209375A (en) Raw material composition for artificial nails, curing method of raw material composition for artificial nails, production method for artificial nails, and artificial nails
JP7044104B2 (en) Curable composition
CN104342011A (en) Nitrogen-gas-protection-free electron-beam-cured coating/ink and preparation and curing methods thereof
JP7231424B2 (en) UV-Curable Coating Composition, Curing Method Thereof, and Cured Coating Film
JP6656662B1 (en) Artificial nail raw material composition, method for curing artificial nail raw material composition, method for producing artificial nail, and artificial nail
CN108997827B (en) Preparation method of UV (ultraviolet) ink
CN103265872A (en) Ultraviolet (UV) glaze and construction method thereof
CN106634507A (en) Roller-coating white elastic photocuring priming paint
CN106566306A (en) Roller painting white elastic light-cured putty
JP7264222B2 (en) light curable nail coating
US20170312793A1 (en) Uv-uvv curable, wear-resistant nail polish
EP4050038A1 (en) Preparation process for solid acrylic resin suitable for uv photocuring system

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: LED-UV phototherapy glue scrubbing-free sealing layer glue and preparation method thereof

Effective date of registration: 20200320

Granted publication date: 20181116

Pledgee: China Co truction Bank Corp Guangzhou green finance reform and innovation pilot area Huadu Branch

Pledgor: UV TECH MATERIAL Ltd.

Registration number: Y2020980000908