CN113402885A - Polyphenylene sulfide composite material with high CTI - Google Patents

Polyphenylene sulfide composite material with high CTI Download PDF

Info

Publication number
CN113402885A
CN113402885A CN202110786219.9A CN202110786219A CN113402885A CN 113402885 A CN113402885 A CN 113402885A CN 202110786219 A CN202110786219 A CN 202110786219A CN 113402885 A CN113402885 A CN 113402885A
Authority
CN
China
Prior art keywords
polyphenylene sulfide
composite material
sulfide composite
magnesium hydroxide
high cti
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.)
Pending
Application number
CN202110786219.9A
Other languages
Chinese (zh)
Inventor
郭建明
王港
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.)
Nanjing Zhenchen Technology Co ltd
Original Assignee
Nanjing Zhenchen 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 Nanjing Zhenchen Technology Co ltd filed Critical Nanjing Zhenchen Technology Co ltd
Priority to CN202110786219.9A priority Critical patent/CN113402885A/en
Publication of CN113402885A publication Critical patent/CN113402885A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/14Glass
    • 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
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • C08K5/134Phenols containing ester groups
    • C08K5/1345Carboxylic esters of phenolcarboxylic acids
    • 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
    • C08K9/00Use of pretreated ingredients
    • C08K9/04Ingredients treated with organic substances
    • C08K9/06Ingredients treated with organic substances with silicon-containing compounds
    • 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
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2217Oxides; Hydroxides of metals of magnesium
    • C08K2003/2224Magnesium hydroxide
    • 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
    • C08K2201/00Specific properties of additives
    • C08K2201/002Physical properties
    • C08K2201/004Additives being defined by their length

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention belongs to the technical field of high polymer materials, and discloses a polyphenylene sulfide composite material with high CTI (comparative tracking index), which consists of polyphenylene sulfide, glass fiber, magnesium hydroxide and a metal passivator, wherein the polyphenylene sulfide composite material comprises the following components in percentage by weight: 20-50% of polyphenylene sulfide, 10-40% of glass fiber, 30-60% of magnesium hydroxide and 1-3% of metal passivator, wherein the polyphenylene sulfide composite material has a high Comparative Tracking Index (CTI), and is suitable for manufacturing electronic and electrical products, mechanical products, automobile parts and other heat-resistant and corrosion-resistant products.

Description

Polyphenylene sulfide composite material with high CTI
Technical Field
The invention relates to the technical field of high polymer materials, in particular to a polyphenylene sulfide composite material with high CTI.
Background
Polyphenylene Sulfide (PPS) has excellent thermal stability, chemical stability, dimensional stability, corrosion resistance, excellent physical and mechanical properties of electrical property, good adhesive property, excellent flame retardance, good electrical property and can be blended and modified. The method has wide application in automobile manufacturing, electronics and electrics, chemical industry, instrument and aerospace industry and the like.
However, due to the existence of a large number of benzene rings on the PPS main chain, when the material is subjected to surface discharge while the rigidity of the material is increased, a large number of radicals are generated due to the breakage of the benzene ring structure, and a conductive carbon layer is formed on the surface, so that the tracking index of the material is relatively low, generally less than 150V, and in order to expand the application range, the electrical property of the material needs to be improved.
The Chinese patent CN112457670A is to add a coupling agent to improve the compatibility of polyphenylene sulfide resin and glass fiber, and to add fluorosilicone oil to improve the tracking index of the material. The Chinese invention patent CN109679345B improves the fluidity of the polyphenylene sulfide composite material by compounding the low molecular weight polymer plasticizer and the modifier, and obviously improves the tracking resistance of the material. Meanwhile, the same tracking resistance of the traditional high-filling-quantity polyphenylene sulfide composite material is achieved by matching a small amount of conductive filler with polyamide resin.
However, the tracking index of these resin composites is less than 300V, and with the increasing use of polyphenylene sulfide materials, especially in the application of electronic and electrical devices, the products require materials with higher fluidity and higher relative tracking index, and the resin composites proposed so far cannot meet higher requirements, so that the development of composites that can simultaneously meet higher molding processability, impact resistance and higher comparative tracking index is required.
Disclosure of Invention
In view of the above, the invention provides a polyphenylene sulfide composite material with high CTI by preparing specific raw materials, and the polyphenylene sulfide composite material has high rigidity, high fluidity, low creep deformation and high electric leakage tracking index, overcomes the defects in the prior art, and is a composite material suitable for popularization and application.
In order to achieve the purpose, the invention adopts the following technical scheme:
the invention provides a polyphenylene sulfide composite material with high CTI, which comprises the following raw materials in percentage by weight:
Figure BDA0003158906420000021
Figure BDA0003158906420000031
preferably, the polyphenylene sulfide resin is linear polyphenylene sulfide; the melt flow rate of the polyphenylene sulfide resin is 400-1200 g/10 min;
specifically, the polyphenylene sulfide resin was tested at 316 ℃ and 5kg for melt flow rate.
Preferably, the glass fiber is a flat glass fiber with an oval cross section; the length of the flat glass fiber is 3-6 mm, and the flat ratio of the cross section is 3-12.
Preferably, the purity of the magnesium hydroxide is 97% or more; the average particle diameter of the magnesium hydroxide is less than 1 mu m;
specifically, the magnesium hydroxide is commercially available magnesium hydroxide, wherein the content of calcium oxide as an impurity is 1% or less, and the content of chlorine as an impurity is 0.5% or less.
Preferably, the metal deactivator is isooctyl 3, 5-di-tert-butyl-4-hydroxyphenylpropionate or N, N' -bis [ beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionyl ] hydrazine;
specifically, the addition of 1-3% of a metal passivator can improve the tracking index (CTI) of the material.
Preferably, the sum of the weight percentages of the magnesium hydroxide and the glass fiber is 50-80%;
specifically, when the sum of the weight percentages of the magnesium hydroxide and the glass fiber is less than 50%, the electrical leakage tracking index of the composite material cannot meet the requirement, and when the sum of the weight percentages of the magnesium hydroxide and the glass fiber is more than 80%, the composite material is difficult to process and has poor mechanical properties.
Preferably, one or more auxiliary agents selected from plasticizers, stabilizers, mold release agents, dyes, pigments and fillers can be added into the polyphenylene sulfide composite material as additives; the dosage of the additive is determined according to the actual production condition.
Preferably, the mixing sequence of the components in the preparation process of the polyphenylene sulfide composite material is not limited and is determined according to the actual production condition; the preparation method of the polyphenylene sulfide composite material is not limited, and the polyphenylene sulfide composite material can be prepared by kneading with an extruder (single-screw or twin-screw extruder), a hot roll, a kneader, a mixing roll or the like; the preparation temperature is 270-340 ℃.
According to the technical scheme, compared with the prior art, the invention has the following beneficial effects:
1. the polyphenylene sulfide composite material has excellent mechanical properties, high rigidity, high fluidity, low creep deformation and the like, has higher Comparative Tracking Index (CTI), and is suitable for manufacturing electronic and electric products, mechanical products, automobile parts and other heat-resistant and corrosion-resistant products.
2. The preparation process of the polyphenylene sulfide composite material is simple and easy to operate, the preparation method and the mixing sequence of the components are not limited, and the polyphenylene sulfide composite material with different characteristics can be obtained by matching with other additives (such as a plasticizer, a stabilizer, a release agent, a dye, a pigment, a filler and the like).
Detailed Description
The invention provides a polyphenylene sulfide composite material with high CTI, which comprises the following raw materials in percentage by weight:
Figure BDA0003158906420000051
in the present invention, the polyphenylene sulfide resin is preferably linear polyphenylene sulfide; the melt flow rate of the polyphenylene sulfide resin is preferably 400-1200 g/10min, and more preferably 400-800g/10 min;
specifically, the polyphenylene sulfide resin was tested at 316 ℃ and 5kg for melt flow rate.
In the present invention, the glass fiber is preferably a flat glass fiber having an elliptical cross section; the length of the flat glass fiber is preferably 3-6 mm, and the cross-section flatness ratio is preferably 3-12.
In the present invention, the purity of the magnesium hydroxide is preferably 97% or more, and more preferably 99%; the average particle diameter of the magnesium hydroxide is preferably 1 μm or less, and more preferably 0.84 μm; the magnesium hydroxide is preferably magnesium hydroxide subjected to surface treatment by a silane coupling agent;
specifically, the magnesium hydroxide is commercially available magnesium hydroxide, wherein the content of calcium oxide as an impurity is 1% or less, and the content of chlorine as an impurity is 0.5% or less.
In the invention, the metal deactivator is 3, 5-di-tert-butyl-4-hydroxy-phenylpropionic acid isooctyl ester or N, N' -bis [ beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionyl ] hydrazine, and is further preferably 3, 5-di-tert-butyl-4-hydroxy-phenylpropionic acid isooctyl ester;
specifically, the Creepage Tracking Index (CTI) of the material can be improved by adding 1-3% of metal passivator.
In the invention, the sum of the weight percentages of the magnesium hydroxide and the glass fiber is preferably 50-80%;
specifically, when the sum of the weight percentages of the magnesium hydroxide and the glass fiber is less than 50%, the electrical leakage tracking index of the composite material cannot meet the requirement, and when the sum of the weight percentages of the magnesium hydroxide and the glass fiber is more than 80%, the composite material is difficult to process and has poor mechanical properties.
In the invention, one or more additives of a plasticizer, a stabilizer, a release agent, a dye, a pigment and a filler can be added into the polyphenylene sulfide composite material as an additive; the dosage of the additive is determined according to the actual production condition.
In the invention, the mixing sequence of the components in the preparation process of the polyphenylene sulfide composite material is not limited and is determined according to the actual production condition; the preparation method of the polyphenylene sulfide composite material is not limited, and the polyphenylene sulfide composite material is preferably prepared by kneading with an extruder (single-screw or twin-screw extruder), a hot roll, a kneader, a mixer, or the like, and more preferably with a single-screw or twin-screw extruder; the preparation temperature is preferably 270-340 ℃, and more preferably 280-300 ℃.
The technical solutions in the embodiments of the present invention will be clearly and completely described below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
The polyphenylene sulfide composite materials prepared in each example and comparative example were injection-molded into test standard bars in standard sizes, and the physical properties in each example were respectively tested in accordance with international standards.
Melt flow rate test conditions: 316 ℃ and 5 kg.
Comparative Tracking Index (CTI) test conditions were tested according to GB/T4207-.
The invention is verified by the following examples and comparative examples, with the following detailed data:
polyphenylene sulfide: PPS, melt flow rate of 400-.
Flat glass fibers: ECS309A-M4, manufactured by Chongqing International composite materials, Inc.;
ordinary glass fiber: ECS11-03-540, manufactured by Megaku corporation of China;
metal passivator: 3, 5-di-tert-butyl-4-hydroxyphenylpropionic acid isooctyl ester, NAUGARD XL-1;
magnesium hydroxide-1: the magnesium hydroxide content is 95%, the average particle size is 0.83 μm, and the magnesium hydroxide is commercially available;
magnesium hydroxide-2: the content of magnesium hydroxide is 99%, the average grain diameter is 1.5 μm, and the magnesium hydroxide is sold in the market;
magnesium hydroxide-3: the magnesium hydroxide has a content of 99%, and has an average particle size of 0.84 μm, and is commercially available;
magnesium hydroxide-4: the content of magnesium hydroxide is 99 percent, the average grain diameter is 0.84 mu m, and the surface is treated by a silane coupling agent and is sold in the market;
calcium carbonate: manufactured by the Shanghai Kindi trade company, Inc.
The formulation tables and the performance test results of examples 1 to 5 and comparative examples 1 to 7 are shown in tables 1 and 2:
TABLE 1 formulation tables and performance test results for examples 1-2 and comparative examples 1-4
Figure BDA0003158906420000081
Figure BDA0003158906420000091
TABLE 2 formulation tables and results of the Performance test for examples 3-5 and comparative examples 5-7
Figure BDA0003158906420000092
Figure BDA0003158906420000101
As can be seen from Table 1, the higher the purity of magnesium hydroxide is, the higher the mechanical properties and the relative tracking index (CTI) of the polyphenylene sulfide composite material are; as can be seen from table 2, the relative tracking index (CTI) of the polyphenylene sulfide composite material using the flat glass fiber is significantly higher than that of the polyphenylene sulfide composite material using the common glass fiber, and the relative tracking index (CTI) of the polyphenylene sulfide composite material prepared using magnesium hydroxide is significantly higher than that of the polyphenylene sulfide composite material prepared using calcium carbonate. As can be seen from tables 1 and 2, the polyphenylene sulfide composite material of the invention not only has excellent mechanical properties, but also has a Comparative Tracking Index (CTI) of more than 400V, which is superior to the CTI of the existing material.
The embodiments in the present description are described in a progressive manner, each embodiment focuses on differences from other embodiments, and the same and similar parts among the embodiments are referred to each other.
The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.

Claims (9)

1. The polyphenylene sulfide composite material with high CTI is characterized by comprising the following raw materials in percentage by weight:
Figure FDA0003158906410000011
2. the polyphenylene sulfide composite material with high CTI as claimed in claim 1, wherein the polyphenylene sulfide resin is linear polyphenylene sulfide.
3. The polyphenylene sulfide composite material with high CTI as claimed in claim 2, wherein the melt flow rate of the polyphenylene sulfide resin is 400-1200 g/10 min.
4. The polyphenylene sulfide composite material with high CTI as claimed in claim 1, wherein the glass fiber is flat glass fiber with an oval cross section.
5. The polyphenylene sulfide composite material with high CTI as claimed in claim 4, wherein the flat glass fiber has a length of 3-6 mm and a cross-sectional flatness ratio of 3-12.
6. The polyphenylene sulfide composite material with high CTI as claimed in claim 1, wherein the purity of the magnesium hydroxide is more than 97%.
7. The polyphenylene sulfide composite material with high CTI as claimed in claim 5, wherein the magnesium hydroxide has an average particle size of 1 μm or less.
8. The polyphenylene sulfide composite material with high CTI as claimed in claim 1, wherein the metal deactivator is isooctyl 3, 5-di-tert-butyl-4-hydroxyphenyl propionate or N, N' -bis [ β (3, 5-di-tert-butyl-4-hydroxyphenyl) propionyl ] hydrazine.
9. The polyphenylene sulfide composite material with high CTI as claimed in claim 1, wherein the sum of the weight percentages of the magnesium hydroxide and the glass fiber is 50-80%.
CN202110786219.9A 2021-07-12 2021-07-12 Polyphenylene sulfide composite material with high CTI Pending CN113402885A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110786219.9A CN113402885A (en) 2021-07-12 2021-07-12 Polyphenylene sulfide composite material with high CTI

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110786219.9A CN113402885A (en) 2021-07-12 2021-07-12 Polyphenylene sulfide composite material with high CTI

Publications (1)

Publication Number Publication Date
CN113402885A true CN113402885A (en) 2021-09-17

Family

ID=77686067

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110786219.9A Pending CN113402885A (en) 2021-07-12 2021-07-12 Polyphenylene sulfide composite material with high CTI

Country Status (1)

Country Link
CN (1) CN113402885A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116574375A (en) * 2023-04-24 2023-08-11 国材(苏州)新材料科技有限公司 Polyphenylene sulfide resin with high CTI value and CTI value test method
CN117186643A (en) * 2023-09-20 2023-12-08 浙江兄弟新材料有限公司 Polyphenylene sulfide composite material with ultrahigh relative electric leakage tracking index and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103013119A (en) * 2012-12-03 2013-04-03 合肥杰事杰新材料股份有限公司 Low-cost modified polyphenylene sulfide composition and preparation method thereof
WO2016050482A1 (en) * 2014-10-01 2016-04-07 Albis Plastic Gmbh Polyphenylene sulfide having a high creep resistance
CN110776742A (en) * 2019-10-09 2020-02-11 中广核俊尔(浙江)新材料有限公司 Polyphenylene sulfide composite material for high-filling low-warpage battery module end plate and preparation method thereof
CN110791095A (en) * 2018-08-01 2020-02-14 山东赛恩吉新材料有限公司 Polyphenylene sulfide composite material and preparation method and application thereof
CN112795191A (en) * 2020-12-29 2021-05-14 上海日之升科技有限公司 High CTI polyphenylene sulfide composite material and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103013119A (en) * 2012-12-03 2013-04-03 合肥杰事杰新材料股份有限公司 Low-cost modified polyphenylene sulfide composition and preparation method thereof
WO2016050482A1 (en) * 2014-10-01 2016-04-07 Albis Plastic Gmbh Polyphenylene sulfide having a high creep resistance
CN110791095A (en) * 2018-08-01 2020-02-14 山东赛恩吉新材料有限公司 Polyphenylene sulfide composite material and preparation method and application thereof
CN110776742A (en) * 2019-10-09 2020-02-11 中广核俊尔(浙江)新材料有限公司 Polyphenylene sulfide composite material for high-filling low-warpage battery module end plate and preparation method thereof
CN112795191A (en) * 2020-12-29 2021-05-14 上海日之升科技有限公司 High CTI polyphenylene sulfide composite material and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116574375A (en) * 2023-04-24 2023-08-11 国材(苏州)新材料科技有限公司 Polyphenylene sulfide resin with high CTI value and CTI value test method
CN117186643A (en) * 2023-09-20 2023-12-08 浙江兄弟新材料有限公司 Polyphenylene sulfide composite material with ultrahigh relative electric leakage tracking index and preparation method thereof

Similar Documents

Publication Publication Date Title
CN113527884A (en) Polyphenylene sulfide composite material with high CTI (comparative tracking index)
CN113402885A (en) Polyphenylene sulfide composite material with high CTI
CN101220183A (en) Environment-protection flame-proof electrostatic resistance polypropylene material and method for producing the same
CN105111772A (en) Low-warpage liquid crystal polymer (LCP) and preparation method thereof
JP2023543072A (en) Halogen-free flame-retardant polyamide composite material and its manufacturing method
CN101633774B (en) PBT molding composite and preparation method thereof
CN105199338A (en) High-performance low-fiber-exposure flame-retardant reinforced PBT composite and preparation method thereof
CN106905674B (en) A kind of Flame-retardant PET and PC composite material and preparation method
CN109320959B (en) Halogen-free high-temperature nylon PA6T reinforced flame-retardant composite material and preparation method thereof
CN109971149B (en) Long-term heat aging resistant halogen-free flame-retardant PC material and preparation method thereof
CN111057376A (en) Polyphenylene sulfide composite material with low flash
JPS62151460A (en) Polyarylene sulfide resin composition
CN115612224B (en) Polyvinyl chloride composite material and preparation method thereof
KR20140092471A (en) Polyester Resin Composition
CN110591267B (en) Low-smoke environment-friendly 5 VA-grade flame-retardant ASA material with excellent weather resistance and preparation method thereof
CN111057374A (en) Low-flash rapid crystalline polyphenylene sulfide composite material
CN114479318B (en) PVC composition with high modulus and preparation method and application thereof
CN106243719A (en) A kind of polyphenylene sulfide composition of high tenacity and preparation method thereof
CN112759904A (en) High-yellowing-resistance flame-retardant PBT (polybutylene terephthalate), and preparation method and application thereof
JP3362061B2 (en) Polyamide resin composition
CN102070886A (en) PBT (polybutylene terephthalate)/PC (polycarbonate) alloy material with high CTI (comparative tracking index) value and high flame retardance and preparation method thereof
CN112226063B (en) Modified polycarbonate composition and preparation method thereof
CN102775745A (en) Flame-retardant glass fiber enhanced PBT (polybutylece terephthalate) composition with high CTI (comparative tracking index) and low precipitating property and preparation thereof
CN109942889B (en) Phosphate-containing composition and application thereof
CN116041933B (en) Halogen-free high-temperature-resistant flame-retardant ABS composite PC alloy material and preparation method and application thereof

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
RJ01 Rejection of invention patent application after publication

Application publication date: 20210917

RJ01 Rejection of invention patent application after publication