CN107163539A - A kind of lightweight makrolon material - Google Patents

A kind of lightweight makrolon material Download PDF

Info

Publication number
CN107163539A
CN107163539A CN201710560928.9A CN201710560928A CN107163539A CN 107163539 A CN107163539 A CN 107163539A CN 201710560928 A CN201710560928 A CN 201710560928A CN 107163539 A CN107163539 A CN 107163539A
Authority
CN
China
Prior art keywords
parts
taken
stirred
lightweight
makrolon
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
CN201710560928.9A
Other languages
Chinese (zh)
Other versions
CN107163539B (en
Inventor
胡敏刚
张宇
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.)
Guangdong Chuangda Yuke Plastic Technology Co ltd
Original Assignee
Suzhou Yuxi New Material Technology 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 Suzhou Yuxi New Material Technology Co Ltd filed Critical Suzhou Yuxi New Material Technology Co Ltd
Priority to CN201710560928.9A priority Critical patent/CN107163539B/en
Publication of CN107163539A publication Critical patent/CN107163539A/en
Application granted granted Critical
Publication of CN107163539B publication Critical patent/CN107163539B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/20General preparatory processes
    • C08G64/30General preparatory processes using carbonates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • C08K2003/265Calcium, strontium or barium carbonate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend

Abstract

The invention discloses a kind of lightweight makrolon material, it is as made from the raw material of following weight parts:140 160 parts of carbonate monomer, 23 parts of pyromellitic acid anhydride, 12 parts of ammonium molybdate, 68 parts of OPE, 10 12 parts of polyether Glycols, vinyl double 0.8 1 parts of stearic amide, 12 parts of calcium acetylacetonate, 10 13 parts of light filler, 12 parts of trimethylolpropane, 0.4 1 parts of 2 mercapto benzimidazole, 35 parts of N methyl pyrrolidones, 0.8 1 parts of sorbitan monooleate, 0.1 0.2 parts of stannous sulfide, 16 20 parts of dry toluenes.Light filler is passed through organic modification by the present invention, then esterification is mixed with the polyester of acid doping, effectively improves dispersiveness of the light filler in polyester matrix, improve the compatibility of light filler and each raw material, the stability_intensity of finished product is improved, the mechanical property of finished product is enhanced.

Description

A kind of lightweight makrolon material
Technical field
The invention belongs to Material Field, and in particular to a kind of lightweight makrolon material.
Background technology
Three big application fields of polycarbonate engineering plastic are glazing, auto industry and electronics, electrical equipment industry, its It is secondary to also have the office equipments such as industrial machinery part, CD, packaging, computer, medical treatment and health care, film, leisure and protector Material etc..Makrolon can be used as door glass, and Polycarbonate Layer pressing plate is widely used in bank, embassy, the house of detention and public place Protective window, for aircraft hatch cover, lighting apparatus, industry security plate washer and bulletproof glass.Polycarbonate plate can make various labels, Such as petrol pump dial plate, fascia, warehouse and outdoor commercial signage, point type slip indicator, polycarbonate resin is used for vapour Car illuminator, instrument panel system and built-in decoration system, as front lamp cover, with plate washer, reflective frame, door before and after reinforcement automobile Frame set, action bars sheath, spoiler, makrolon are employed to be used as terminal box, socket, plug and sleeve pipe, pad, TV conversion The connector of communication cable under device, telephone line support, switch box, telephone exchange, distribution disc elements, relay1 case gathers Carbonic ester can make low load part, for household electrical appliance motor, vacuum cleaner, device for washing one's hair, coffee machine, bread baker, power The handle of instrument, various gears, worm gear, axle sleeve, lead rule, shelf in refrigerator.Makrolon is the preferable material of disc storage medium Material.Polycarbonate bottles are transparent, lightweight, impact resilience is good, resistance to certain high temperature and etchant solution washing, are used as recoverable Bottle.Makrolon and polycarbonate alloy can do computer rack, shell and subsidiary engine, printer part.The resistance to height of modified polycarbonate Energy radio sterilization, resistance to boiling and baking disinfecting, available for blood sampling sample utensil, blood oxygenators, surgical operating instrument, Rend dialysis Device etc., makrolon can make the helmet and safety cap, protective face mask, sunglasses and motion cover glass.Polycarbonate film is widely used in Print chart, medical packaging, membrane type commutator.The application and development of makrolon is to high compound, high function, customizations, series Change direction to develop, be proposed the multiple products such as CD, automobile, office equipment, casing, packaging, medicine, illumination, film each The special grade trade mark;
But the packing quality weight such as magnesium hydroxide, graphene added in traditional makrolon material, with polymeric matrix Poor compatibility, is easily reduced the mechanical property of finished-product material.
The content of the invention
It is an object of the invention to the packing quality weight such as the magnesium hydroxide for adding in the prior art, graphene, with gathering The poor compatibility of compound matrix, there is provided a kind of lightweight makrolon material for the problem of being easily reduced the mechanical property of finished-product material.
To achieve the above object, the present invention uses following technical scheme:
A kind of lightweight makrolon material, it is as made from the raw material of following weight parts:
It is 140-160 parts of carbonate monomer, 2-3 parts of pyromellitic acid anhydride, 1-2 parts of ammonium molybdate, 6-8 parts of OPE, poly- 10-12 parts of ether dihydric alcohol, vinyl double 0.8-1 parts of stearic amide, 1-2 parts of calcium acetylacetonate, 10-13 parts of light filler, three 1-2 parts of hydroxymethyl-propane, 0.4-1 parts of 2- mercapto benzimidazoles, 3-5 parts of 1-METHYLPYRROLIDONE, sorbitan monooleate 0.8-1 parts, 0.1-0.2 parts of stannous sulfide, 16-20 parts of dry toluene.
Described carbonate monomer is trimethylene carbonate.
Described light filler is that weight ratio is 4-6:1 precipitated calcium carbonate, diatomite mixing composition.
Described lightweight makrolon material, it is made by following steps:
(1)Take in 2- mercapto benzimidazoles, the absolute ethyl alcohol for being added to 10-15 times of its weight, stir, rise temperature is 60-70 DEG C, trimethylolpropane is added, insulated and stirred 4-10 minutes obtains alcohol alkane solution;
(2)Polyether Glycols are taken, insulated and stirred 5-6 minutes at 70-80 DEG C, OPE is added, stirs, send into Into 130-140 DEG C of oil bath, insulated and stirred 10-20 minutes, discharging is mixed with calcium acetylacetonate, ammonium molybdate, is stirred to normal Temperature, obtains polythene wax emulsion;
(3)Sorbitan monooleate, dry toluene mixing are taken, stirs, obtains toluene solution;
(4)Carbonate monomer, pyromellitic acid anhydride mixing are taken, is added in above-mentioned toluene solution, stirs, is sent to anti- Answer in kettle, be passed through nitrogen, regulation temperature of reaction kettle is 140-145 DEG C, add catalyst, sealing thermal insulation 17-20 hours discharges, Obtain acid doping makrolon;
(5)Above-mentioned alcohol alkane solution, polythene wax emulsion mixing are taken, stirs, adds above-mentioned light filler, stannous sulfide, surpass Sound 3-5 minutes, must organise filler slurry;
(6)Above-mentioned acid doping makrolon, the filler slurry that organises mixing are taken, the deionization of 2-3 times of compound weight is added to In water, stir, add the double stearic amides of 1-METHYLPYRROLIDONE, vinyl, rise temperature is 70-75 DEG C, and insulation is stirred Mix 1-2 hours, filter, precipitation is washed, dried completely at 80-90 DEG C of vacuum, produce the lightweight makrolon material.
Wherein, described catalyst is stannous octoate, and consumption is the 1-2% of carbonate monomer weight.
Advantages of the present invention:
The present invention is mixed with carbonate monomer, pyromellitic acid anhydride, using toluene emulsion as solvent, is obtained under catalyst action 2- mercapto benzimidazoles, are then distributed in silanol solution, the alcohol with OPE is molten by acid doping makrolon Liquid is mixed, and light filler is carried out into organic modification, the filler slurry that then will organise is mixed with acid doping makrolon, is carried out In esterification, the aqueous solution for being subsequently dispersed resin acid acid amides, then by filtration drying, produce;
The present invention uses precipitated calcium carbonate, diatomite as light filler, by organic modification, then with the polyester of acid doping Mixing esterification, effectively improves dispersiveness of the light filler in polyester matrix, improves light filler and the phase of each raw material Capacitive, improves the stability_intensity of finished product, enhances the mechanical property of finished product.
Embodiment
With reference to embodiment, the present invention will be further described.
Embodiment 1
By weight, each raw material is weighed:160 parts of carbonate monomer trimethylene carbonate, 3 parts of pyromellitic acid anhydride, molybdenum It is double 1 part of the stearic amides of sour 2 parts of ammonium, 8 parts of OPE, 12 parts of polyether Glycols, vinyl, 2 parts of calcium acetylacetonate, light The smooth single oil of 13 parts of matter filler, 2 parts of trimethylolpropane, 0.4 part of 2- mercaptos benzimidazole, 5 parts of 1-METHYLPYRROLIDONE, sorb 1 part of acid esters, 0.2 part of stannous sulfide, 20 parts of dry toluene.
Wherein, described light filler is that weight ratio is 6:1 precipitated calcium carbonate, diatomite mixing composition.
Each raw material weighed is carried out to prepare lightweight makrolon material, specific preparation process is:
(1)2- mercapto benzimidazoles are taken, in the absolute ethyl alcohol for being added to 15 times of its weight, are stirred, rise temperature is 70 DEG C, trimethylolpropane is added, insulated and stirred 10 minutes obtains alcohol alkane solution;
(2)Polyether Glycols are taken, insulated and stirred 6 minutes at 80 DEG C add OPE, stir, be sent to 140 DEG C oil bath in, insulated and stirred 20 minutes, discharging, mix with calcium acetylacetonate, ammonium molybdate, stirring to normal temperature, obtain Tissuemat E Emulsion;
(3)Sorbitan monooleate, dry toluene mixing are taken, stirs, obtains toluene solution;
(4)Carbonate monomer, pyromellitic acid anhydride mixing are taken, is added in above-mentioned toluene solution, stirs, is sent to anti- Answer in kettle, be passed through nitrogen, regulation temperature of reaction kettle is 145 DEG C, add octoate catalyst stannous, consumption is carbonate monomer weight 2%, sealing thermal insulation 20 hours, discharging, obtain acid doping makrolon;
(5)Above-mentioned alcohol alkane solution, polythene wax emulsion mixing are taken, stirs, adds above-mentioned light filler, stannous sulfide, surpass Sound 5 minutes, must organise filler slurry;
(6)Above-mentioned acid doping makrolon, the filler slurry that organises mixing are taken, the deionized water of 3 times of compound weight is added to In, stir, add the double stearic amides of 1-METHYLPYRROLIDONE, vinyl, rise temperature is 75 DEG C, and insulated and stirred 2 is small When, precipitation is washed in filtering, is dried completely at 90 DEG C of vacuum, is produced the lightweight makrolon material.
Embodiment 2
By weight, each raw material is weighed:140 parts of carbonate monomer trimethylene carbonate, 2 parts of pyromellitic acid anhydride, molybdenum Double 0.8 part of the stearic amides of sour 1 part of ammonium, 6 parts of OPE, 10 parts of polyether Glycols, vinyl, 1 part of calcium acetylacetonate, 10 parts of light filler, 1 part of trimethylolpropane, 0.4 part of 2- mercaptos benzimidazole, 3 parts of 1-METHYLPYRROLIDONE, the smooth list of sorb 0.8 part of oleate, 0.1 part of stannous sulfide, 16 parts of dry toluene.
Described light filler is that weight ratio is 4:1 precipitated calcium carbonate, diatomite mixing composition.
Each raw material weighed is carried out to prepare lightweight makrolon material, specific preparation process is:
(1)2- mercapto benzimidazoles are taken, in the absolute ethyl alcohol for being added to 10 times of its weight, are stirred, rise temperature is 60 DEG C, trimethylolpropane is added, insulated and stirred 4 minutes obtains alcohol alkane solution;
(2)Polyether Glycols are taken, insulated and stirred 5 minutes at 70 DEG C add OPE, stir, be sent to 130 DEG C oil bath in, insulated and stirred 10 minutes, discharging, mix with calcium acetylacetonate, ammonium molybdate, stirring to normal temperature, obtain Tissuemat E Emulsion;
(3)Sorbitan monooleate, dry toluene mixing are taken, stirs, obtains toluene solution;
(4)Carbonate monomer, pyromellitic acid anhydride mixing are taken, is added in above-mentioned toluene solution, stirs, is sent to anti- Answer in kettle, be passed through nitrogen, regulation temperature of reaction kettle is 140 DEG C, add octoate catalyst stannous, consumption is carbonate monomer weight 1%, sealing thermal insulation 17 hours, discharging, obtain acid doping makrolon;
(5)Above-mentioned alcohol alkane solution, polythene wax emulsion mixing are taken, stirs, adds above-mentioned light filler, stannous sulfide, surpass Sound 3 minutes, must organise filler slurry;
(6)Above-mentioned acid doping makrolon, the filler slurry that organises mixing are taken, the deionized water of 2 times of compound weight is added to In, stir, add the double stearic amides of 1-METHYLPYRROLIDONE, vinyl, rise temperature is 70 DEG C, and insulated and stirred 1 is small When, precipitation is washed in filtering, is dried completely at 80 DEG C of vacuum, is produced the lightweight makrolon material.
Performance test:
Traditional makrolon material, the lightweight makrolon material of the embodiment of the present invention 1 and 2 are taken, the test piece of same size is made, Tensile strength is measured under the conditions of ASTM D-638 respectively, contrast test is then carried out:
As a result:The tensile strength of lightweight makrolon material prepared by the embodiment of the present invention 1 and 2 is 45-50MPa, traditional poly- carbon The tensile strength of acid esters is 20MPa;
The proportion of the test piece of the embodiment of the present invention 1 and 2 is 0.8-0.85g/cm3, traditional makrolon test piece proportion be 1.15g/ cm3
As can be seen that the makrolon material of the present invention has more preferable tensile strength compared to traditional makrolon, quality is more Gently.

Claims (5)

1. a kind of lightweight makrolon material, it is characterised in that it is as made from the raw material of following weight parts:
It is 140-160 parts of carbonate monomer, 2-3 parts of pyromellitic acid anhydride, 1-2 parts of ammonium molybdate, 6-8 parts of OPE, poly- 10-12 parts of ether dihydric alcohol, vinyl double 0.8-1 parts of stearic amide, 1-2 parts of calcium acetylacetonate, 10-13 parts of light filler, three 1-2 parts of hydroxymethyl-propane, 0.4-1 parts of 2- mercapto benzimidazoles, 3-5 parts of 1-METHYLPYRROLIDONE, sorbitan monooleate 0.8-1 parts, 0.1-0.2 parts of stannous sulfide, 16-20 parts of dry toluene.
2. a kind of lightweight makrolon material according to claim 1, it is characterised in that described carbonate monomer is three Carbonate.
3. a kind of lightweight makrolon material according to claim 1, it is characterised in that described light filler is weight Than for 4-6:1 precipitated calcium carbonate, diatomite mixing composition.
4. a kind of lightweight makrolon material according to claim 1, it is characterised in that it is made by following steps:
(1)Take in 2- mercapto benzimidazoles, the absolute ethyl alcohol for being added to 10-15 times of its weight, stir, rise temperature is 60-70 DEG C, trimethylolpropane is added, insulated and stirred 4-10 minutes obtains alcohol alkane solution;
(2)Polyether Glycols are taken, insulated and stirred 5-6 minutes at 70-80 DEG C, OPE is added, stirs, send into Into 130-140 DEG C of oil bath, insulated and stirred 10-20 minutes, discharging is mixed with calcium acetylacetonate, ammonium molybdate, is stirred to normal Temperature, obtains polythene wax emulsion;
(3)Sorbitan monooleate, dry toluene mixing are taken, stirs, obtains toluene solution;
(4)Carbonate monomer, pyromellitic acid anhydride mixing are taken, is added in above-mentioned toluene solution, stirs, is sent to anti- Answer in kettle, be passed through nitrogen, regulation temperature of reaction kettle is 140-145 DEG C, add catalyst, sealing thermal insulation 17-20 hours discharges, Obtain acid doping makrolon;
(5)Above-mentioned alcohol alkane solution, polythene wax emulsion mixing are taken, stirs, adds above-mentioned light filler, stannous sulfide, surpass Sound 3-5 minutes, must organise filler slurry;
(6)Above-mentioned acid doping makrolon, the filler slurry that organises mixing are taken, the deionization of 2-3 times of compound weight is added to In water, stir, add the double stearic amides of 1-METHYLPYRROLIDONE, vinyl, rise temperature is 70-75 DEG C, and insulation is stirred Mix 1-2 hours, filter, precipitation is washed, dried completely at 80-90 DEG C of vacuum, produce the lightweight makrolon material.
5. a kind of lightweight makrolon material according to claim 4, it is characterised in that step 4)Described in catalyst For stannous octoate, consumption is the 1-2% of carbonate monomer weight.
CN201710560928.9A 2017-07-11 2017-07-11 A kind of lightweight makrolon material Active CN107163539B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710560928.9A CN107163539B (en) 2017-07-11 2017-07-11 A kind of lightweight makrolon material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710560928.9A CN107163539B (en) 2017-07-11 2017-07-11 A kind of lightweight makrolon material

Publications (2)

Publication Number Publication Date
CN107163539A true CN107163539A (en) 2017-09-15
CN107163539B CN107163539B (en) 2019-03-01

Family

ID=59823724

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710560928.9A Active CN107163539B (en) 2017-07-11 2017-07-11 A kind of lightweight makrolon material

Country Status (1)

Country Link
CN (1) CN107163539B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107556730A (en) * 2017-10-17 2018-01-09 孙爱芬 A kind of macromolecule radioresistance environmental protection polyester material and preparation method thereof
CN108706916A (en) * 2018-06-25 2018-10-26 邱朝转 A kind of interior wall is except formaldehyde absorbing coating and preparation method thereof
CN108745313A (en) * 2018-06-14 2018-11-06 黄益良 A kind of cladded type sewage-treating agent and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080085390A1 (en) * 2006-10-04 2008-04-10 Ryan Thomas Neill Encapsulation of electrically energized articles
CN105061971A (en) * 2015-06-16 2015-11-18 华南理工大学 Method for preparing completely-degradable composite material through acid anhydride and microcrystalline cellulose synergetic modification on poly(propylene carbonate)

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080085390A1 (en) * 2006-10-04 2008-04-10 Ryan Thomas Neill Encapsulation of electrically energized articles
CN105061971A (en) * 2015-06-16 2015-11-18 华南理工大学 Method for preparing completely-degradable composite material through acid anhydride and microcrystalline cellulose synergetic modification on poly(propylene carbonate)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107556730A (en) * 2017-10-17 2018-01-09 孙爱芬 A kind of macromolecule radioresistance environmental protection polyester material and preparation method thereof
CN108745313A (en) * 2018-06-14 2018-11-06 黄益良 A kind of cladded type sewage-treating agent and preparation method thereof
CN108706916A (en) * 2018-06-25 2018-10-26 邱朝转 A kind of interior wall is except formaldehyde absorbing coating and preparation method thereof

Also Published As

Publication number Publication date
CN107163539B (en) 2019-03-01

Similar Documents

Publication Publication Date Title
CN107163539A (en) A kind of lightweight makrolon material
CN100467557C (en) Production of cryogenic direct-welding polyurethane envelope without pinhole
CN102731755B (en) Method for preparing plasticizer
CN107523257A (en) A kind of cold curing demulsification acetoacetic ester type silicone sealant
CN103641696B (en) Method for synthesizing dihydroxypropyl bisphenol A ether through one-step process
CN110078903A (en) A method of continuously preparing Biodegradable resin side by side
CN110408012A (en) The preparation method of 1,2- polybutadiene rubber toughening modified polylactic acid
CN103408863A (en) Infrared reflective material and membrane prepared therefrom
CN104277222A (en) Phenyl hydrogen-containing silicone resin for LED encapsulation and preparation method of phenyl hydrogen-containing silicone resin
CN105131297A (en) Phenyl vinyl MQ resin and preparation method thereof
CN101775125A (en) Non-aromatic nucleus structure poly-hexahydrobenzene phthalic anhydride dihydric alcohol ester plasticizer and preparation method thereof
CN103289095A (en) A synthesis method of high viscosity alpha, omega-dihydroxy polydimethylsiloxane
CN107141759B (en) A kind of preparation method of lightweight makrolon material
CN101565500B (en) Polyester/clay nanometer composite material, special catalyst thereof and methods for preparing polyester/clay nanometer composite material and special catalyst thereof
CN111117428A (en) Multifunctional anti-static protective film and preparation method thereof
CN1635039A (en) Method for preparing novel B level high speed polyurethane enamelled wire paint
CN107556730A (en) A kind of macromolecule radioresistance environmental protection polyester material and preparation method thereof
CN107099025B (en) A kind of preparation method of titanium sol deposition makrolon material
CN108530860A (en) A kind of light-weight environment-friendly makrolon material and preparation method thereof
CN102453249B (en) Catalyst composition
CN109721997A (en) A kind of graphene toughening polyester material and preparation method thereof
CN109679083A (en) A kind of polycarbonate anti-static sheath material and preparation method thereof
CN111004119A (en) Preparation method of bis (2-hydroxyethyl) terephthalate
CN111040457A (en) Preparation method of curing coated flame-retardant waterproof agent for plastics
CN104263278A (en) Cross-linking agent used by LED (light-emitting diode) packaging adhesive and preparation method of cross-linking agent

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20210121

Address after: 215400 No. 20, Jian Xiong Road, science and Education Town, Taicang, Suzhou, Jiangsu

Patentee after: SUZHOU YUANLUE INTELLECTUAL PROPERTY OPERATION Co.,Ltd.

Address before: 215400 1 1 Beijing West Road, Taicang Economic Development Zone, Suzhou, Jiangsu.

Patentee before: SUZHOU YUXI NEW MATERIAL TECHNOLOGY Co.,Ltd.

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20240118

Address after: 523000 Room 101, No. 1, Jinwei Road, Zhangmutou town, Dongguan City, Guangdong Province

Patentee after: Guangdong Chuangda Yuke Plastic Technology Co.,Ltd.

Address before: 215400 No. 20, Jian Xiong Road, science and Education Town, Taicang, Suzhou, Jiangsu

Patentee before: SUZHOU YUANLUE INTELLECTUAL PROPERTY OPERATION CO.,LTD.