CN111171408B - Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof - Google Patents

Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof Download PDF

Info

Publication number
CN111171408B
CN111171408B CN202010092357.2A CN202010092357A CN111171408B CN 111171408 B CN111171408 B CN 111171408B CN 202010092357 A CN202010092357 A CN 202010092357A CN 111171408 B CN111171408 B CN 111171408B
Authority
CN
China
Prior art keywords
rubber
content
fatty acid
rubber compound
acid ester
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.)
Active
Application number
CN202010092357.2A
Other languages
Chinese (zh)
Other versions
CN111171408A (en
Inventor
许茂祥
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.)
Changxin Rubber Industry Shanghai Co ltd
Original Assignee
Changxin Rubber Industry Shanghai 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 Changxin Rubber Industry Shanghai Co ltd filed Critical Changxin Rubber Industry Shanghai Co ltd
Priority to CN202010092357.2A priority Critical patent/CN111171408B/en
Publication of CN111171408A publication Critical patent/CN111171408A/en
Application granted granted Critical
Publication of CN111171408B publication Critical patent/CN111171408B/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
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/02Organic and inorganic ingredients
    • 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
    • C08K3/02Elements
    • C08K3/04Carbon
    • 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
    • C08K3/02Elements
    • C08K3/06Sulfur
    • 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
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • 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
    • C08K5/10Esters; Ether-esters
    • C08K5/11Esters; Ether-esters of acyclic polycarboxylic 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
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/39Thiocarbamic acids; Derivatives thereof, e.g. dithiocarbamates
    • C08K5/40Thiurams, i.e. compounds containing groups
    • 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
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/45Heterocyclic compounds having sulfur in the ring
    • C08K5/46Heterocyclic compounds having sulfur in the ring with oxygen or nitrogen in the ring
    • C08K5/47Thiazoles
    • 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
    • C08K2201/003Additives being defined by their diameter
    • 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
    • C08K2201/006Additives being defined by their surface area
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/80Technologies aiming to reduce greenhouse gasses emissions common to all road transportation technologies
    • Y02T10/86Optimisation of rolling resistance, e.g. weight reduction 

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 relates to the technical field of rubber application, in particular to a low-content polycyclic aromatic hydrocarbon rubber compound and a preparation method thereof. In the rubber compound, the content of benzo (a) pyrene is less than 0.1mg/kg, and the content of benzo (e) pyrene is less than 0.1 mg/kg. The invention provides a rubber compound, which can reduce the content of polycyclic aromatic hydrocarbon in the rubber compound by selecting proper preparation raw materials, ensure safety, and can be used for materials which are directly or indirectly contacted with a human body, such as toys, tableware, office supplies and the like; in addition, by selecting proper preparation raw materials, the invention can effectively relieve the reduction of tensile strength, elasticity and flexing resistance caused by using an effective sulfur vulcanization system, thereby improving the overall performance and the use stability of the rubber compound.

Description

Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof
Technical Field
The invention relates to the technical field of rubber application, in particular to a low-content polycyclic aromatic hydrocarbon rubber compound and a preparation method thereof.
Background
Polycyclic Aromatic Hydrocarbons (PAHs) are Hydrocarbons formed by bonding two or more benzene rings, and are harmful substances generated from fuels such as petroleum and coal, and wood and combustible gases under incomplete combustion or high-temperature treatment conditions. It is commonly present in petrochemicals, rubber, plastics, lubricating oil, rust preventive oil, incompletely combusted organic compounds, and is one of the important carcinogenic substances in the environment. In addition, human activities such as automobile exhaust gas, residential heating systems, waste combustion, hot cracking of petroleum, factory boiler combustion emissions, etc. are also major sources of PAHs.
The rubber is widely applied in production and life of people, for example, tableware, office supplies, toys and the like are frequently contacted with the skin or oral cavity of a human body, if too many PAHs exist in the rubber, the health of the human body is easily damaged, and detailed requirements are made on the PAHs in GS certification of German product safety Committee (AfPS), wherein the maximum total content of polycyclic aromatic hydrocarbons of 1 type of materials (the contact time is more than 30s) of materials which are put in the mouth or materials which are contacted with the skin on the toys is limited to 1mg/kg, and the maximum content of benzo (a) pyrene is limited to 0.2 mg/kg. The preparation of rubber mixtures with a low polycyclic aromatic hydrocarbon content is therefore currently of importance.
Disclosure of Invention
In order to solve the above problems, the first aspect of the present invention provides a low-content polycyclic aromatic hydrocarbon rubber composition containing benzo (a) pyrene in an amount of less than 0.1mg/kg and benzo (e) pyrene in an amount of less than 0.1 mg/kg.
According to a preferable technical scheme, the preparation raw materials of the rubber compound comprise, by weight, 90-120 parts of nitrile rubber, 55-75 parts of filler, 8-13 parts of plasticizer, 0.1-0.8 part of sulfur, 2-5 parts of vulcanization accelerator, 0.1-2 parts of softener and 0.1-2 parts of anti-aging agent.
As a preferable technical scheme of the invention, the Mooney viscosity ML1+4 of the nitrile rubber at 100 ℃ is 40-50, and the content of acrylonitrile is 25-30 wt%.
In a preferred embodiment of the present invention, the filler is one or more selected from carbon black, talc, kaolin, zinc oxide, graphene, white carbon black, kaolin, calcium carbonate, graphite, sericite powder, and illite.
As a preferable technical scheme of the invention, the filler comprises carbon black and zinc oxide, and the weight ratio is (10-15): 1.
as a preferable technical scheme of the invention, the average particle size of the carbon black is 40-60 nm, and the specific surface area is 34-55 m 2 /g。
As a preferable technical scheme of the invention, the plasticizer comprises short-chain saturated fatty acid ester and long-chain saturated fatty acid ester, and the weight ratio of the short-chain saturated fatty acid ester to the long-chain saturated fatty acid ester is 1: (0.01-0.1).
In a preferred embodiment of the present invention, the vulcanization accelerator is one or more selected from the group consisting of a sulfonamide vulcanization accelerator, a thiuram vulcanization accelerator, a guanidine vulcanization accelerator, a dithiocarbamate vulcanization accelerator, and a thiazole vulcanization accelerator.
In a preferred embodiment of the present invention, the softening agent is one or more selected from mineral oil, animal and vegetable oil, and fatty acid.
In a second aspect, the present invention provides a method for preparing a low polycyclic aromatic hydrocarbon compound as described above, comprising the steps of:
premixing: mixing the nitrile rubber, the filler, the plasticizer and the anti-aging agent to obtain a premix;
mixing: adding sulfur, a vulcanization accelerator and a softening agent into the premix, mixing and vulcanizing to obtain the rubber compound.
Compared with the prior art, the invention has the following beneficial effects: the invention provides a rubber compound, which can reduce the content of polycyclic aromatic hydrocarbon in the rubber compound by selecting proper preparation raw materials, ensure safety, and can be used for materials which are directly or indirectly contacted with a human body, such as toys, tableware, office supplies and the like; in addition, by selecting proper preparation raw materials, the invention can effectively relieve the reduction of tensile strength, elasticity and flexing resistance caused by using an effective sulfur vulcanization system, thereby improving the overall performance and the use stability of the rubber compound.
Detailed Description
The disclosure may be understood more readily by reference to the following detailed description of preferred embodiments of the invention and the examples included therein. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In case of conflict, the present specification, including definitions, will control.
The term "prepared from …" as used herein is synonymous with "comprising". As used herein, the terms "comprises," "comprising," "includes," "including," "has," "having," "contains" or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a composition, process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, process, method, article, or apparatus.
The conjunction "consisting of …" excludes any unspecified elements, steps or components. When an amount, concentration, or other value or parameter is expressed as a range, preferred range, or as a range of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. For example, when a range of "1 to 5" is disclosed, the described range should be interpreted to include the ranges "1 to 4", "1 to 3", "1 to 2 and 4 to 5", "1 to 3 and 5", and the like. When a range of values is described herein, unless otherwise stated, the range is intended to include the endpoints thereof and all integers and fractions within the range.
The singular forms "a," "an," and "the" include plural referents unless the context clearly dictates otherwise. "optional" or "any" means that the subsequently described event or events may or may not occur, and that the description includes instances where the event occurs and instances where it does not.
In addition, the indefinite articles "a" and "an" preceding an element or component of the invention are not intended to limit the number requirement (i.e., the number of occurrences) of the element or component. Thus, "a" or "an" should be read to include one or at least one, and the singular form of an element or component also includes the plural unless the stated number clearly indicates that the singular form is intended.
The present invention is illustrated by the following specific embodiments, but is not limited to the specific examples given below.
The invention provides a polycyclic aromatic hydrocarbon compound with low content, wherein the content of benzo (a) pyrene in the compound is less than 0.1mg/kg, and the content of benzo (e) pyrene in the compound is less than 0.1 mg/kg.
In a preferred embodiment, the raw materials for preparing the rubber compound comprise, by weight, 90-120 parts of nitrile rubber, 55-75 parts of filler, 8-13 parts of plasticizer, 0.1-0.8 part of sulfur, 2-5 parts of vulcanization accelerator, 0.1-2 parts of softener and 0.1-2 parts of anti-aging agent.
In a preferred embodiment, the raw materials for preparing the rubber compound of the present invention comprise, by weight, 100 parts of nitrile rubber, 65 parts of filler, 10.5 parts of plasticizer, 0.6 part of sulfur, 3 parts of vulcanization accelerator, 1 part of softener and 1 part of antioxidant.
Sulfur
Sulfur is also called sulfur, colloidal sulfur, sulfur block. The appearance is light yellow brittle crystal or powder, and has special odor. Molecular weight 32.06, vapor pressure 0.13kPa, flash point 207 ℃, melting point 118 ℃, boiling point 444.6 ℃, relative density (water 1) 2.0. Sulfur is insoluble in water, slightly soluble in ethanol and ether, and easily soluble in carbon disulfide. Sulfur is widely used in the rubber field as a vulcanizing agent for rubber. The sulfur can be prepared or purchased by self without specific limitation. In a preferred embodiment, the sulfur of the present invention is available from Zhongya chemical Co.
Vulcanization accelerator
Vulcanization accelerators are referred to as accelerators for short. A substance capable of promoting vulcanization. Can shorten the vulcanizing time, reduce the vulcanizing temperature, reduce the consumption of vulcanizing agents, improve the physical and mechanical properties of rubber and the like. The vulcanization accelerator is not particularly limited in the present invention.
In one embodiment, the vulcanization accelerator of the present invention is selected from one or more of sulfonamide vulcanization accelerators, thiuram vulcanization accelerators, guanidine vulcanization accelerators, dithiocarbamate vulcanization accelerators, and thiazole vulcanization accelerators.
As examples of the sulfonamide vulcanization accelerators, there are included, but not limited to, N-t-butyl-2-benzothiazolesulfenamide (TBBS), 2-Mercaptobenzothiazole (MBT), sodium or zinc salt of 2-mercaptobenzothiazole (ZMBT), benzothiazole-2-Dicyclohexylsulfenamide (DCBS), benzothiazole disulfide (MBTS), tetrabenzylthiuram disulfide (TBzTD), N-cyclohexyl-2-benzothiazolesulfenamide (CZ); in a preferred embodiment, the sulfonamide vulcanization accelerator of the present invention is N-cyclohexyl-2-benzothiazolesulfenamide; in a more preferred embodiment, the N-cyclohexyl-2-benzothiazolesulfenamide of the present invention is purchased from Zhengzhou double strength chemical products, Inc.
As examples of the thiuram-based vulcanization accelerators, there may be mentioned, but not limited to, tetramethylthiuram monosulfide (TMTM), tetramethylthiuram disulfide (TMTD), tetraethylthiuram disulfide (TETD), bis (1, 5-pentamethyleneidenedithiuram tetrasulfide (DPTT); in a preferred embodiment, the thiuram-based vulcanization accelerator of the present invention is tetramethylthiuram disulfide; in a more preferred embodiment, the tetramethylthiuram disulfide of the present invention is purchased from Zhengzhou Dougli chemical products, Inc.
As examples of guanidine vulcanization accelerators, there are included, but not limited to, Diphenylguanidine (DPG), Triphenylguanidine (TPG), diorthotolylene tetralone (DOTG), Orthotolylbiguanide (OTBG), guanidine salts (nitrate, carbonate, acetate, thiocyanate, sulfate), and derivatives thereof.
Examples of the dithiocarbamate vulcanization accelerator include, but are not limited to, zinc dimethyldithiocarbamate (PZ), Zinc Diethyldithiocarbamate (ZDC), zinc dibutyldithiocarbamate (BZ), zinc ethylphenyldithiocarbamate (PX).
Examples of thiazole vulcanization accelerators include, but are not limited to, accelerator M, accelerator DM, accelerator MZ.
Preferably, the vulcanization accelerator comprises a sulfonamide vulcanization accelerator and a thiuram vulcanization accelerator in a weight ratio of (2-3): (2-3); further, the weight ratio of the sulfonamide vulcanization accelerator to the thiuram vulcanization accelerator is 1: 1.
the invention uses low-dosage sulfur and high-dosage accelerator as an effective sulfur vulcanization system, and the sulfur dosage of the vulcanization system is very small, so that the single-sulfur or double-sulfur cross-linking bond generated in the vulcanized rubber structure has absolute advantages, generally reaches more than 90 percent, and the vulcanization reversion phenomenon does not occur after over-vulcanization, and the obtained vulcanized rubber has excellent heat resistance, compression deformation resistance and aging resistance of the vulcanized rubber and small heat generation. However, compared with the common sulfur vulcanization system with more sulfur, the vulcanized rubber vulcanized by the effective vulcanization system has poor tensile strength, elasticity and fatigue resistance, such as poor yield resistance and flexibility, due to the factors of low content of polysulfide crosslinking bonds and the like.
Filler
Filler generally refers to a material filled in other objects. In chemical products, the filler is also called filler, which is a solid material for improving processability and mechanical properties of products and/or reducing cost.
In one embodiment, the filler of the present invention is selected from one or more of carbon black, talc, kaolin, zinc oxide, graphene, white carbon, china clay, calcium carbonate, graphite, sericite powder and illite.
Preferably, the filler comprises carbon black and zinc oxide, and the weight ratio is (10-15): 1; further, the weight ratio of the carbon black and the zinc oxide is 12: 1.
carbon black, also known as carbon black, is an amorphous carbon. Light, loose and extremely fine black powder with very large surface area ranging from 10 to 3000m 2 The carbon-containing substance is a product obtained by incomplete combustion or thermal decomposition of a carbon-containing substance (coal, natural gas, heavy oil, fuel oil, etc.) under the condition of insufficient air. The structural properties of carbon black are expressed by the degree of chain-like or grape-like aggregation among carbon black particles. The higher the carbon black structure, the more easily a space network channel is formed and the less easily destroyed. The high-structure carbon black has fine particles, closely packed reticular chains, large specific surface area and more particles per unit mass. The carbon black of the present invention may be purchased or manufactured by oneself; in a preferred embodiment, the carbon black of the present invention is obtained from Cabot's LP series carbon black, such as Spheron SO-LP (average particle size of 40 to 60nm, specific surface area of 34 to 55 m) 2 (g), Spheron 4000-LP (the average particle diameter is 61-100 nm, and the specific surface area is 20-33 m) 2 (g), Vulcan 6-LP (average particle diameter of 20-25 nm, specific surface area of 109-123 m) 2 (iv)/g); in a more preferred embodiment, the carbon black of the present invention is Spheron SO-LP.
The average particle diameter is an average particle diameter of an actual particle group consisting of particles having different sizes and shapes, and is referred to as a spherical particle diameter if the overall lengths of the particle diameters are the same as compared with a hypothetical particle group consisting of uniform spherical particles. Can be tested according to methods well known in the art.
The specific surface area refers to the total area of the material per unit mass. The unit is m 2 (ii) in terms of/g. The specific surface area in the present invention is a specific surface area measured by the CTAB method.
Zinc oxide is an oxide of zinc. Is insoluble in water and soluble in acid and strong base. Zinc oxide is a commonly used chemical additive, and is widely applied to the manufacture of products such as plastics, silicate products, synthetic rubber, lubricating oil, paint, coating, ointment, adhesive, food, batteries, flame retardant and the like. The invention does not limit the zinc oxide specifically, and can be made by oneself or purchased; in a preferred embodiment, the zinc oxide of the present invention is available from Nks132, national island nacartane new materials technology ltd.
More preferably, the carbon black has an average particle diameter of 40 to 60nm and a specific surface area of 34 to 55m 2 /g。
The invention is favorable for increasing the tensile strength, the elongation at break and the flexibility of vulcanized rubber by using carbon black and zinc oxide as fillers, especially carbon black and zinc oxide with certain particle size and specific surface area, which is probably because the carbon black and zinc oxide can play a role of reinforcement by adding the carbon black and zinc oxide, on one hand, the smaller particle size and the larger specific surface area of the carbon black are favorable for increasing the contact between the carbon black and rubber and increasing the physical adsorption between the rubber and the carbon black, in addition, the carbon black contains active sites with larger activity on the surface and can generate chemical adsorption with the rubber, on the other hand, the zinc oxide can play a role of filling and can also play a role of combining with a softening agent such as stearic acid to promote the crosslinking density, and the combination of the two fillers forms a physical and chemical crosslinking network with more proper density, the nitrile rubber molecular chain is easy to slip, and simultaneously, the chemical sites can be utilized to transfer stress, so that brittle fracture is reduced.
However, it should be noted that, compared with the common sulfur vulcanization system mainly having the S-S bond breakage under the action of tensile force, the effective vulcanization system mainly has the C-S bond breakage, and compared with the S-S bond with lower bond energy, the C-S is not easily broken and also not easily generated, so that the force of the broken part cannot be transferred to other chains during repeated flexing, and the reinforcing effect of carbon black and zinc oxide cannot be well embodied.
In addition, when the proper carbon black, such as the LP series carbon black of cabot, is selected in the invention, compared with the common carbon black, such as ASTM N650, N683, N539 or N550 carbon black, the polycyclic aromatic hydrocarbon content of the prepared rubber compound is low, the rubber compound meets the requirement of environment-friendly products, and the safety is increased when the rubber compound is particularly used for products which may be contained in the mouth, such as toys and the like. When carbon black having a larger specific surface area or a smaller particle diameter and zinc oxide are used as fillers in the present invention, the flex resistance, tensile strength and elasticity are not further increased, which may be caused by the adsorption of too much nitrile rubber around the carbon black.
Softening agent
The softener is an assistant for improving the processing performance and the use performance of rubber, can increase the plasticity of rubber, reduce the viscosity of the rubber and the temperature during mixing, improve the dispersibility and the mixing property, and improve the tensile strength, the elongation and the wear resistance of vulcanized rubber.
In one embodiment, the softener of the present invention is selected from one or more of mineral oil, animal and vegetable oil, and fatty acid.
Examples of the mineral oil include, but are not limited to, paraffinic mineral oil, naphthenic mineral oil, and aromatic mineral oil.
Examples of animal and vegetable oils include, but are not limited to, rapeseed oil, castor oil, cottonseed oil, linseed oil, soybean oil, sesame oil, corn oil, safflower oil, palm oil, coconut oil, peanut oil, wood wax, rosin, pine tar, tall oil.
As examples of fatty acids, including, but not limited to, stearic acid, palmitic acid, lauric acid, lignoceric acid, arachidic acid; in a preferred embodiment, the fatty acid of the present invention is stearic acid; in a more preferred embodiment, the stearic acid of the present invention is purchased from PALMATA1801 of indolylbox.
Nitrile rubber
The nitrile rubber is prepared from butadiene and acrylonitrile by an emulsion polymerization method, is mainly produced by a low-temperature emulsion polymerization method, and has the advantages of excellent oil resistance, higher wear resistance, better heat resistance and strong bonding force. The disadvantages are poor low temperature resistance, ozone resistance, poor insulation properties and slightly low elasticity. The acrylonitrile butadiene rubber contains 42-46% of acrylonitrile, 36-41% of acrylonitrile, 31-35% of acrylonitrile, 25-30% of acrylonitrile, 18-24% of acrylonitrile and the like. The more the acrylonitrile content, the better the oil resistance, but the lower the cold resistance. It can be used in air at 120 deg.C or oil at 150 deg.C for a long period. In addition, it has excellent water resistance, air tightness and excellent adhesion performance. The rubber is widely used for manufacturing various oil-resistant rubber products, various oil-resistant gaskets, sleeves, flexible packages, flexible rubber tubes, printing and dyeing rubber rollers, cable rubber materials and the like, and becomes an essential elastic material in the industries of automobiles, aviation, petroleum, copying and the like. The nitrile rubber can be purchased or manufactured by self; in a preferred embodiment, the nitrile rubber according to the invention is selected from one or more of the Perbunan series nitrile rubber, Krynac series nitrile rubber, Baymod series nitrile rubber, Therban series nitrile rubber, langen series nitrile rubber, germany; in a more preferred embodiment, the nitrile rubber of the present invention is a Perbunan series nitrile rubber.
Examples of Perbunan series nitrile rubbers include, but are not limited to, 2255VP, 2845F, 2870F, 2895F, 3430F, 3470F, 3945F, 3965F, 1846F, 4456F; in a more preferred embodiment, the nitrile rubbers of the Perbunan series according to the invention are selected from 1846F (Mooney ML1+4 at 100 ℃ C. is 46, acrylonitrile content is 18 wt.%), 2845F (Mooney ML1+4 at 100 ℃ C. is 45, acrylonitrile content is 28 wt.%), 2870F (Mooney ML1+4 at 100 ℃ C. is 70, acrylonitrile content is 28 wt.%), 3945F (Mooney ML1+4 at 100 ℃ C. is 45, acrylonitrile content is 39 wt.%); in a more preferred embodiment, the Perbunan series nitrile rubber according to the invention is 1846F.
Mooney viscosity, also known as rotational (Mooney) viscosity, is a value measured by Mooney viscometer, and can basically reflect the degree of polymerization and molecular weight of synthetic rubber, and rubber materials with high Mooney viscosity are not easy to be uniformly mixed and extruded, and have high molecular weight and wide distribution range. The rubber material with low Mooney viscosity is easy to stick to the roller, and has low molecular weight and narrow distribution range. Too low a Mooney viscosity results in a cured article having low tensile strength. Can be tested according to methods well known in the art, such as ISO289/ASTM D1646.
The acrylonitrile content is the weight percentage of acrylonitrile in the nitrile rubber and can be determined according to methods known in the art, and can be listed as SH/T1157, GB 4486.
In one embodiment, the nitrile rubber of the present invention has a Mooney viscosity ML1+4 at 100 ℃ of 40 to 50 and an acrylonitrile content of 25 to 30 wt%; further, the nitrile rubber of the present invention has a Mooney viscosity ML1+4 at 100 ℃ of 45 and an acrylonitrile content of 28 wt%.
When the acrylonitrile butadiene rubber with specific viscosity and acrylonitrile content and carbon black and zinc oxide are used for combined action, the carbon black and zinc oxide reinforcing action is further exerted, which is probably because when the acrylonitrile butadiene rubber with Mooney viscosity of 40-50, namely with proper molecular weight and fluidity is used, the acrylonitrile butadiene rubber is beneficial to uniform dispersion with fillers, and brittle fracture caused by uneven dispersion of the fillers is reduced, in addition, the molecular weight of acrylonitrile and butadiene monomers in the acrylonitrile butadiene rubber is controlled, so that the content of carbon-carbon double bonds and nitrile groups in the acrylonitrile butadiene rubber is controlled, and proper polarity and crosslinking sites are obtained, so that a uniform chemical crosslinking system can be formed with a vulcanization system, carbon black and the like, the formation of cavities is reduced, the reinforcement of the carbon black and zinc oxide is promoted, in addition, the acrylonitrile with lower content is used, the relaxation time caused by large intermolecular action force of the acrylonitrile butadiene rubber is favorably reduced when stress is applied, the impact on elasticity and repeated flexing performance, and the acrylonitrile branched chain in the nitrile rubber is also beneficial to increasing the physical and even chemical adsorption of broken C-S bonds and high-polarity acrylonitrile when breakage is formed by repeated flexing, increasing the branching and passivating degree of the breakage, reducing apparent breakage and increasing flexing resistance.
And if nitrile rubbers with too high a viscosity or too high an acrylonitrile content are used in the present invention, the elasticity and flex resistance of the rubber mixtures according to the invention are adversely affected by too high a crosslinking density or polarity.
Plasticizer
The plasticizer is added into the polymer material to increase the plasticity of the polymer, so that the performance of the polymer material can be improved, the production cost is reduced, and the production benefit is improved. The plasticizer mainly has the effects of weakening the secondary valence bonds among resin molecules, increasing the mobility of the molecular bonds of the resin, reducing the crystallinity of the resin molecules, increasing the plasticity of the resin molecules, enhancing the flexibility of the resin molecules, being easy to process, being legally applicable to industrial application, and being widely existed in food packaging, cosmetics, medical devices and environmental water. Such as cling film, food packaging, toys, etc. Plasticizers include saturated fatty acid esters, phthalates (dimethyl phthalate (DMP), diethyl phthalate (DEP), di-n-butyl phthalate (DBP), dioctyl phthalate (DOP), Butyl Benzyl Phthalate (BBP), di-2-ethyl hexyl phthalate (DEHP), dioctyl phthalate (DOP), diisononyl phthalate (DINP), benzene polyesters, benzoates, polyol esters, chlorinated hydrocarbons, epoxies, citrates, polyesters, and the like. Wherein the long-term contact of the phthalate ester can cause chronic poisoning to human body, especially can influence the endocrine system and reproductive system of human, therefore, nowadays, European and American countries have gradually made strict regulations or direct forbidding to toys, food, daily necessities, medical supplies, textiles, etc. which are added with the phthalate ester plasticizer.
In one embodiment, the plasticizer of the present invention is a fatty acid ester plasticizer.
The aliphatic dibasic acid ester plasticizer has the advantages of excellent low-temperature performance, high plasticizing efficiency and good viscosity performance, but has poor compatibility, oil resistance and electrical insulation performance compared with phthalate, and is expensive, and most of the aliphatic dibasic acid ester plasticizer is used as a plasticizer aid. The aliphatic dibasic acid esters are classified into saturated fatty acid dibasic acid esters and unsaturated fatty acid dibasic acid esters. The unsaturated fatty acid dibasic acid ester can be copolymerized with vinyl monomers due to the double bond contained in the molecule, and can be used as an internal plasticizer, such as di (2-ethyl) hexyl adipate (DOA), so that the plasticizing efficiency is high, the thermal discoloration is small, and the good low-temperature flexibility and light resistance can be endowed to products; the disadvantages are high volatility, poor water resistance, migration resistance and electric insulation and high price. In a preferred embodiment, the plasticizer of the present invention is a saturated fatty acid ester plasticizer.
Preferably, the plasticizer comprises short-chain saturated fatty acid ester and long-chain saturated fatty acid ester, and the weight ratio of the short-chain saturated fatty acid ester to the long-chain saturated fatty acid ester is 1: (0.01 to 0.1); further, the weight ratio of the short-chain saturated fatty acid ester to the long-chain saturated fatty acid ester is 1: 0.05.
the short-chain saturated fatty acid ester is a saturated fatty acid ester with a chain length of less than or equal to 25, and comprises but is not limited to succinate, glutarate, adipate, suberate, azelate and sebacate, and in a preferred embodiment, the short-chain saturated fatty acid ester is selected from one or more of di (2-ethyl) adipate (DOA), di (2-ethyl) adipate (DOS), di-sec-octyl sebacate (DCS) and dibutyl sebacate (DBS); in a more preferred embodiment, the short chain saturated fatty acid ester of the present invention is di (2-ethyl) hexyl adipate, available from Shangyng Shanghai chemical Co., Ltd.
The long-chain saturated fatty acid ester is a saturated fatty acid ester with a chain length of more than 25, and includes, but is not limited to, WB222, WB212, WB42 and WA48 of struktol; in a more preferred embodiment, the long chain saturated fatty acid ester of the present invention is struktol's WB 222.
The invention unexpectedly finds that when short-chain saturated fatty acid ester and long-chain fatty acid ester are used as dispersing agents, the dispersing of nitrile rubber and filler can be promoted, and the tensile strength and elasticity are promoted, and meanwhile, the increase of the flexibility resistance is facilitated. This is probably because, by adding short-chain saturated fatty acid ester, such as diisooctyl adipate and long-chain saturated fatty acid ester, such as WB222, on one hand, the short-chain saturated fatty acid ester, such as isooctyl adipate, has a shorter alkyl chain and is compatible with nitrile rubber, and the ester group and the alkyl chain in the molecule can respectively isolate the nitrile group and the molecular chain in nitrile rubber, and on the other hand, the long-chain saturated fatty acid ester, such as WB222, shields the nitrile group in nitrile rubber, and simultaneously, the low-polarity long alkyl chain forms micelles, and through the shielding and micelle effects of the two, the acting force between nitrile rubbers can be further reduced, so that the viscosity is further reduced, the flow of nitrile rubber is promoted, the dispersion between nitrile rubber and filler is promoted, thereby promoting the exertion of the filler reinforcing effect, and increasing the tensile strength and the elongation at break; in addition, in the repeated flexing process, compared with nitrile rubber, the fatty acid ester plasticizer with lower molecular weight can move smoothly in the flexing process, so that abrasion caused by interaction between molecular chains in the flexing process is reduced, and because of larger polarity difference of saturated fatty acid ester, particularly long-chain saturated fatty acid ester and nitrile rubber, the long-chain saturated fatty acid ester tends to be adsorbed on the surfaces of carbon black and zinc oxide, the separation between the zinc oxide and a nitrile rubber matrix in the repeated flexing process is reduced, and the increase of flexing resistance is facilitated.
Anti-aging agent
Rubber and its products become sticky, hard, brittle or cracked during long-term storage and use due to the action of heat, oxygen, ozone, valence-changing metal ions, mechanical stress, light, high-energy rays, and other chemicals and mold. This phenomenon of deterioration of physical and mechanical properties and of elasticity with time is called aging. As the aging process progresses and progresses, the properties of the rubber and its products gradually decrease to completely lose the use value. To this end, certain chemicals, called anti-aging agents, are added to the rubber and its products to increase its resistance to the above-mentioned destructive effects and to retard or inhibit the aging process, thereby extending the shelf life and useful life of the rubber and its products. The present invention is not particularly limited to an antioxidant, and there may be mentioned antioxidant AW (6-ethoxy-2, 2, 4-trimethyl-1, 2-dihydroquinoline), antioxidant a (N-phenyl- α -aniline), antioxidant D (N-phenyl- β -naphthylamine), antioxidant CPPD (N-phenyl-N '-cyclohexyl-p-phenylenediamine), antioxidant H (N-N' -diphenyl-p-phenylenediamine), 4-bis (2, 2-dimethylbenzyl) diphenylamine, and antioxidant RD (2,2, 4-trimethyl-1, 2-dihydroquinoline).
In one embodiment, the antioxidant according to the present invention is antioxidant RD.
The anti-aging agent RD is suitable for natural rubber and synthetic rubber such as butyronitrile, butylbenzene, ethylene propylene, chloroprene and the like, has excellent effect of preventing aging caused by heat and oxygen, but has poor effect of preventing flex aging. In a preferred embodiment, the antioxidant RD of the present invention is obtained from Zhengzhou double strength chemical products, Inc.
In a second aspect, the present invention provides a method for preparing a low polycyclic aromatic hydrocarbon compound as described above, comprising the steps of:
premixing: mixing the nitrile rubber, the filler, the plasticizer and the anti-aging agent to obtain a premix;
mixing: adding sulfur, a vulcanization accelerator and a softening agent into the premix, mixing and vulcanizing to obtain the rubber compound.
In a preferred embodiment, in the vulcanization of the present invention, primary vulcanization and secondary vulcanization are sequentially carried out; further, the temperature of primary vulcanization is 160-180 ℃, and the time is 4-6 min; furthermore, the temperature of the secondary vulcanization is 130-150 ℃, and the time is 50-80 min.
Examples
The present invention will be specifically described below by way of examples. It should be noted that the following examples are only for illustrating the present invention and should not be construed as limiting the scope of the present invention, and that the insubstantial modifications and adaptations of the present invention by those skilled in the art based on the above disclosure are still within the scope of the present invention.
A1: nitrile rubber
The nitrile rubber is 1846F from the Langshan Perbunan series of Germany.
A2: nitrile rubber
The nitrile rubber is 2845F of the Langshan Perbunan series of Germany.
A3: nitrile rubber
The nitrile rubber is 2870F of the langerhans Perbunan series of germany.
B1: filler material
The filler was carbon black, available from Spheron SO-LP of Cambot.
B2: filler material
The filler was carbon black, available from Spheron 4000-LP of Cambot.
B3: filler material
The filler was carbon black, available from Vulcan 6-LP of cabot.
B4: filler material
The filler was zinc oxide, available from Nks132, national island nacarton new materials science and technology ltd.
C1: plasticizer
The plasticizer is adipic acid di (2-ethyl) hexyl ester and is purchased from Shangying Shanghai Shandong Shanghai Kagaku Kogyo Co.
C2: plasticizer
The plasticizer is bis (2-ethyl) hexyl sebacate, and is purchased from Shangying Shanghai Shandong Shanghai Kagaku Kogyo Co.
C3: plasticizer
The plasticizer is WB222 from struktol.
C4: plasticizer
The plasticizer is WB212 from struktol.
D: sulfur
The sulfur was purchased from Zhongya chemical Co., Ltd.
E1: vulcanization accelerator
The vulcanization accelerator is N-cyclohexyl-2-benzothiazole sulfonamide and is purchased from Zhengzhou double-strength chemical products Co.
E2: vulcanization accelerator
The vulcanization accelerator is tetramethyl thiuram disulfide, which is purchased from Zhengzhou double-strength chemical products Co.
F: softening agent
The softener is stearic acid, available from PALMATA1801 of indolylboro.
G: anti-aging agent
The anti-aging agent is an anti-aging agent RD purchased from Zhengzhou double-strength chemical products Limited company.
TABLE 1
Figure GDA0003690885300000121
Figure GDA0003690885300000131
Attached Table 1
Figure GDA0003690885300000132
Figure GDA0003690885300000141
Examples 1-13 provide low polycyclic aromatic hydrocarbon compounds having the formulations shown in Table 1, in parts by weight.
Embodiments 1 to 13 provide a low polycyclic aromatic hydrocarbon compound, including the following steps:
premixing: mixing the nitrile rubber, the filler, the plasticizer and the anti-aging agent to obtain a premix;
mixing: and adding sulfur, a vulcanization accelerator and a softening agent into the premix, mixing, and then sequentially carrying out primary vulcanization and secondary vulcanization to obtain the rubber compound, wherein the temperature of the primary vulcanization is 170 ℃, the time is 5min, and the temperature of the secondary vulcanization is 140 ℃, and the time is 60 min.
Evaluation of Performance
1. Polycyclic aromatic hydrocarbon content: the low content polycyclic aromatic hydrocarbon compound provided in examples 1-3 was prepared according to AfPS GS 2014: 01PAK method test, 18 kinds of aromatic hydrocarbons are analyzed by GC-MS, wherein MDI is the detection limit of the method, ND is not detected, namely < MDI, "-" is not specified, 18 kinds of aromatic hydrocarbons are not detected when the MDL is 0.1mg/kg, which indicates that the content of the 18 kinds of aromatic hydrocarbons is less than 0.1mg/kg, and meets the standard of 1 kind of materials in the GS certification of AfPS, wherein Table 2 is the detection result of the mixed rubber provided by example 1, MDI is the detection limit of the method, ND is not detected, namely < MDI, "-" is not specified.
TABLE 2 polycyclic aromatic Hydrocarbon test results
Figure GDA0003690885300000142
Figure GDA0003690885300000151
2. Tensile strength: the low-content polycyclic aromatic hydrocarbon compounds provided in the examples were subjected to tensile strength tests in accordance with GB T528-.
3. Elongation at break: the low-content polycyclic aromatic hydrocarbon compounds provided in the examples were tested for elongation at break according to GB T528-1992 and rated, with a rating of 1 being 200% or less, a rating of 2 being greater than 200% and 240% or less, a rating of 3 being greater than 240% and 270% or less, a rating of 4 being greater than 270% and 300% or less, and a rating of 5 being greater than 300% and the results are given in Table 3.
4. Flex resistance: the low-content polycyclic aromatic hydrocarbon compounds provided in the examples were subjected to a flex resistance test in accordance with GB/T13934-1992, and the degree of cracking was measured at 15 ten thousand flex times, the results being shown in Table 3.
TABLE 3 mechanical Properties test
Figure GDA0003690885300000152
Figure GDA0003690885300000161
5. And (3) performance characterization test: the hardness, tensile strength, elongation at break, tear strength, stress at elongation at break of 100%, 200% and 300%, density, primary vulcanization shrinkage and secondary vulcanization shrinkage of the low-content polycyclic aromatic hydrocarbon compound as provided in example were measured, and the results are shown in Table 4.
Table 4 characterization test of properties
Examples 1
Shore hardness 71
Tensile strength/MPa 16.77
Elongation at break% 308
Tear strength MPa 72
100% stress at definite elongation/MPa 4.53
200% stress at definite elongation/MPa 10.77
300% stress at definite elongation/MPa 16.42
Density g/cm3 1.173
Shrinkage in first vulcanization% 2.11
Shrinkage ratio of secondary vulcanization% 2.14
The test results in table 2 show that the low-content polycyclic aromatic hydrocarbon rubber compound provided by the invention has low polycyclic aromatic hydrocarbon content, meets the AfPSGS detection standard, and can avoid harm of polycyclic aromatic hydrocarbon to human body; in addition, as can be seen from the results in tables 3 and 4, by using appropriate raw materials and preparation processes, it is also advantageous to improve the mechanical properties and the like, to obtain a rubber compound with good comprehensive properties, and to further expand the application range.
The foregoing examples are merely illustrative and serve to explain some of the features of the method of the present invention.

Claims (2)

1. A low-content polycyclic aromatic hydrocarbon rubber compound is characterized in that the content of benzo (a) pyrene in the rubber compound is less than 0.1mg/kg, and the content of benzo (e) pyrene in the rubber compound is less than 0.1 mg/kg;
the preparation raw materials of the rubber compound comprise, by weight, 90-120 parts of nitrile rubber, 55-75 parts of filler, 8.5-12.5 parts of plasticizer, 0.6 part of sulfur, 3 parts of vulcanization accelerator, 1 part of softener and 1 part of anti-aging agent;
the Mooney viscosity ML1+4 of the nitrile rubber at 100 ℃ is 46, and the content of acrylonitrile is 18 wt%;
the filler comprises carbon black and zinc oxide, and the weight ratio is (10-14): 1; the carbon black has an average particle diameter of 40 to 60nm and a specific surface areaThe product is 34 to 55m 2 /g;
The plasticizer comprises short-chain saturated fatty acid ester and long-chain saturated fatty acid ester, and the weight ratio of the short-chain saturated fatty acid ester to the long-chain saturated fatty acid ester is 1: (0.01 to 0.1); the short-chain saturated fatty acid ester is adipic acid di (2-ethyl) hexyl ester, and the long-chain saturated fatty acid ester is WB222 of struktol;
the vulcanization accelerator is N-cyclohexyl-2-benzothiazole sulfonamide and tetramethyl thiuram disulfide, and the weight ratio of the vulcanization accelerator is 1: 1;
the softening agent is stearic acid;
the anti-aging agent is an anti-aging agent RD.
2. A method for preparing a low polycyclic aromatic hydrocarbon compound according to claim 1, comprising the steps of:
premixing: mixing the nitrile rubber, the filler, the plasticizer and the anti-aging agent to obtain a premix;
mixing: adding sulfur, a vulcanization accelerator and a softening agent into the premix, mixing and vulcanizing to obtain the rubber compound.
CN202010092357.2A 2020-02-14 2020-02-14 Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof Active CN111171408B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010092357.2A CN111171408B (en) 2020-02-14 2020-02-14 Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010092357.2A CN111171408B (en) 2020-02-14 2020-02-14 Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof

Publications (2)

Publication Number Publication Date
CN111171408A CN111171408A (en) 2020-05-19
CN111171408B true CN111171408B (en) 2022-08-23

Family

ID=70653080

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010092357.2A Active CN111171408B (en) 2020-02-14 2020-02-14 Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof

Country Status (1)

Country Link
CN (1) CN111171408B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113024910A (en) * 2021-03-05 2021-06-25 安徽中鼎密封件股份有限公司 Nitrile rubber product material with low polycyclic aromatic hydrocarbon content

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102167853A (en) * 2011-02-18 2011-08-31 青岛开世密封工业有限公司 Formula and preparation method of nitrile-butadiene rubber for speed-reducing clutch oil seal
CN104403159A (en) * 2014-12-09 2015-03-11 赵慧江 Rubber and preparation method thereof
WO2015049982A1 (en) * 2013-10-04 2015-04-09 昭和電工株式会社 Method for producing rubber compounding oil, rubber compounding oil, rubber composition and tire
CN105482188A (en) * 2014-09-19 2016-04-13 扬州华通橡塑有限公司 Formula of low-temperature-resistant nitrile rubber
CN107400479A (en) * 2016-05-19 2017-11-28 于学德 A kind of nitrile butadiene rubber sealant
CN109679167A (en) * 2018-12-29 2019-04-26 苏州恒则成精密橡塑有限公司 A kind of nitrile rubber of environmental protection
CN110551331A (en) * 2019-08-15 2019-12-10 芜湖集拓橡胶技术有限公司 nitrile rubber meeting Reach environment-friendly requirement
CN110643090A (en) * 2019-09-29 2020-01-03 芜湖集拓橡胶技术有限公司 Nitrile rubber meeting PAHS2 type environmental protection requirements

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102167853A (en) * 2011-02-18 2011-08-31 青岛开世密封工业有限公司 Formula and preparation method of nitrile-butadiene rubber for speed-reducing clutch oil seal
WO2015049982A1 (en) * 2013-10-04 2015-04-09 昭和電工株式会社 Method for producing rubber compounding oil, rubber compounding oil, rubber composition and tire
CN105482188A (en) * 2014-09-19 2016-04-13 扬州华通橡塑有限公司 Formula of low-temperature-resistant nitrile rubber
CN104403159A (en) * 2014-12-09 2015-03-11 赵慧江 Rubber and preparation method thereof
CN107400479A (en) * 2016-05-19 2017-11-28 于学德 A kind of nitrile butadiene rubber sealant
CN109679167A (en) * 2018-12-29 2019-04-26 苏州恒则成精密橡塑有限公司 A kind of nitrile rubber of environmental protection
CN110551331A (en) * 2019-08-15 2019-12-10 芜湖集拓橡胶技术有限公司 nitrile rubber meeting Reach environment-friendly requirement
CN110643090A (en) * 2019-09-29 2020-01-03 芜湖集拓橡胶技术有限公司 Nitrile rubber meeting PAHS2 type environmental protection requirements

Also Published As

Publication number Publication date
CN111171408A (en) 2020-05-19

Similar Documents

Publication Publication Date Title
JP5536376B2 (en) Carbon nanotube-containing rubber composition
CA2925928C (en) Rubber compositions and uses thereof
JP2007269259A (en) Pneumatic radial tire
EP2334722B2 (en) Hnbr compositions with very high filler levels having excellent processability and resistance to aggressive fluids
JPWO2008123405A1 (en) Nitrile copolymer rubber composition and nitrile copolymer latex composition
CN110892017B (en) Fluororubber composition, process for producing the same, and fluororubber crosslinked molded article
CN111171408B (en) Low-content polycyclic aromatic hydrocarbon rubber compound and preparation method thereof
US20170260340A1 (en) Styrene-butadiene rubber (sbr)-nanocarbon filled masterbatches and uses thereof
CN103642097A (en) Preparation method of nitrile butadiene rubber for preparing seal ring of floating oil seal with high wear resistance
CN107383508A (en) A kind of modified chloroprene rubber and preparation method thereof
CN105111642B (en) A kind of 4 third fluorubber with low compression set performance and preparation method thereof
WO2013133358A1 (en) Method for producing nitrile copolymer rubber composition
Raju et al. A study on the use of castor oil as plasticizer in natural rubber compounds
WO2013021586A1 (en) Rubber composition and pneumatic tire using same
JP7143604B2 (en) Rubber composition for vulcanized bladder and vulcanized bladder
Al-maamori et al. Effect of carbon black on mechanical and physical properties of acrylonitrile butadiene rubber (NBR) composite
EP1559585B1 (en) Rubber composition for a tire and pneumatic tire using the same
CN107189143A (en) A kind of compounding rubber of oil-resisting type
KR101379333B1 (en) Curing bladder composition for tire and curing bladder manufactured by using the same
CN113493580A (en) Styrene butadiene rubber-based rubber composition, vulcanized rubber, and preparation method and application thereof
CN113493579A (en) Composition for rubber sealing material, vulcanized rubber, and preparation method and application thereof
JP2008239832A (en) Rubber composition, crosslinked rubber and molded product
KR101457864B1 (en) Rubber composition for tire tread and tire manufactured by using the same
CN106117681A (en) A kind of neoprene/graphene composite material and preparation method thereof
DE102022121721A1 (en) METHOD OF INCORPORATING GRAPHENE INTO A RUBBER COMPOUND USING A LIQUID PLASTICIER LINE PROCESS - LPR PROCESS

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