CN106807347A - A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric - Google Patents

A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric Download PDF

Info

Publication number
CN106807347A
CN106807347A CN201710261345.6A CN201710261345A CN106807347A CN 106807347 A CN106807347 A CN 106807347A CN 201710261345 A CN201710261345 A CN 201710261345A CN 106807347 A CN106807347 A CN 106807347A
Authority
CN
China
Prior art keywords
parts
thermal cracking
carbon monoxide
olefin polymeric
mixture
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.)
Withdrawn
Application number
CN201710261345.6A
Other languages
Chinese (zh)
Inventor
施享
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.)
Maanshan Niuze Technology Service Co Ltd
Original Assignee
Maanshan Niuze Technology Service 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 Maanshan Niuze Technology Service Co Ltd filed Critical Maanshan Niuze Technology Service Co Ltd
Priority to CN201710261345.6A priority Critical patent/CN106807347A/en
Publication of CN106807347A publication Critical patent/CN106807347A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/16Clays or other mineral silicates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/10Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal from rubber or rubber waste
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/10Feedstock materials
    • C10G2300/1003Waste materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Materials Engineering (AREA)
  • Catalysts (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

The invention discloses a kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric, carbon monoxide-olefin polymeric includes 10 30 parts of 5 25 parts of al binder, 10 35 parts of zirconium oxide, 15 55 parts of natural mineral matter, 10 30 parts of clay, 5 20 parts of tridecyl trimethylammonium bromide, 8 20 parts of citric acid and absolute ethyl alcohol by weight, preparation process is simple of the present invention, preparation process is environment friendly and pollution-free, obtained carbon monoxide-olefin polymeric good stability, scrap rubber thermal cracking efficiency can be effectively improved, while improve the yield and quality of the oil product that thermal cracking is obtained.

Description

A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric
Technical field
The present invention relates to thermal cracking catalyst preparation technical field, specially a kind of scrap rubber thermal cracking catalyst group Compound.
Background technology
The rubber of early stage is taken from the latex of the plants such as rubber tree, Russian dandelion, be made after processing with elasticity, insulation Property, the material of impermeable water and air.Elastomeric macromolecular compound.It is divided into two kinds of natural rubber and synthetic rubber.Natural rubber Glue is made of the extraction colloid post-processing from the plants such as rubber tree, Russian dandelion;Synthetic rubber is then by the aggregated reaction of various monomers And obtain.Rubber is widely used in industry or life each side, makes with the booming of rubber industry and its on a large scale With waste rubber goodses bring serious social concern with rubber rubbish --- energy waste and pollution environment, it is necessary to useless Rubber carries out thermal cracking treatment.
Catalytic pyrolysis are a kind of in the presence of a catalyst using heavy oil production ethene and the method for producing propylene, with energy consumption Low, ingredient requirement is low, the characteristics of product slates flexible adjustment.The reaction temperature of catalytic pyrolysis (CPP) technique is higher, reachable 600 DEG C, therefore it is required that used catalyst has good heat and hydrothermal stability, become in particular with cracking stock and deteriorate again, Its harshness raising of operation, requirements at the higher level are proposed to catalytic thermal cracking catalyst.Existing thermal cracking makes work with catalyst Skill is complicated.Cost of manufacture is high, and obtained poor catalyst stability, is had little effect in thermal cracking efficiency to improving.
The content of the invention
It is an object of the invention to provide a kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric, to solve above-mentioned background technology The problem of middle proposition.
To achieve the above object, the present invention provides following technical scheme:A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric, Carbon monoxide-olefin polymeric includes al binder 5-25 parts, zirconium oxide 10-35 parts, natural mineral matter 15-55 parts, clay by weight 10-30 parts, 5-20 parts, citric acid 8-20 parts and absolute ethyl alcohol 10-30 parts of tridecyl trimethylammonium bromide.
Preferably, the natural mineral matter uses 30% kaolin, 20% montmorillonite, 10% diatomite, 10% hydrotalcite, 10% The mixture of bentonite, 20% rectorite composition.
Preferably, preferred composition proportion is:15 parts of binding agent, 28 parts of zirconium oxide, 35 parts of natural mineral matter, clay 20 Part, 15 parts of tridecyl trimethylammonium bromide, 15 parts of citric acid and 20 parts of absolute ethyl alcohol.
Preferably, its preparation method is comprised the following steps:
A, will natural mineral matter, zirconium oxide, clay mix after add pulverizer in crush, 1/3 al binder is added afterwards, stir It is mixed to form mixture A;
B, addition tridecyl trimethylammonium bromide, absolute ethyl alcohol in mixture A, mixture are added in adding water-bath Heat, between 45 DEG C -65 DEG C, constant temperature 30min after heating 45min-55min obtains mixture B to the temperature control of water-bath;
C, 2/3 al binder is added in mixture B, carry out being sufficiently mixed stirring afterwards, until temperature is down to room temperature, Zhi Houjing 2h is put, after then sediment is washed, is dried, then the roasting that heats up obtains thermal cracking catalyst.
Preferably, pulverizer specific breakage rate is 1500-3000 revs/min in the step A, and grinding time is 15min- 35min。
Compared with prior art, the beneficial effects of the invention are as follows:Preparation process is simple of the present invention, preparation process environmental protection is without dirt Dye, obtained carbon monoxide-olefin polymeric good stability can effectively improve scrap rubber thermal cracking efficiency, while improve thermal cracking The yield and quality of the oil product for obtaining;In addition, the preparation method that the present invention is used is simple to operate, preparation efficiency is high, can enter one Step improves the activity and anti-wear performance of catalyst.
Specific embodiment
The technical scheme in the embodiment of the present invention is clearly and completely described below, it is clear that described embodiment Only a part of embodiment of the invention, rather than whole embodiments.Based on the embodiment in the present invention, the common skill in this area The every other embodiment that art personnel are obtained under the premise of creative work is not made, belongs to the model of present invention protection Enclose.
The present invention provides a kind of technical scheme:A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric, carbon monoxide-olefin polymeric is pressed Parts by weight include al binder 5-25 parts, zirconium oxide 10-35 parts, natural mineral matter 15-55 parts, clay 10-30 parts, tridecane 5-20 parts, citric acid 8-20 parts and absolute ethyl alcohol 10-30 parts of base trimethylammonium bromide.
Embodiment one:
The composition proportion for using for:5 parts of al binder, 10 parts of zirconium oxide, 15 parts of natural mineral matter, 10 parts of clay, tridecyl 10 parts of 5 parts of trimethylammonium bromide, 8 parts of citric acid and absolute ethyl alcohol.
In the present embodiment, natural mineral matter uses 30% kaolin, 20% montmorillonite, 10% diatomite, 10% hydrotalcite, 10% The mixture of bentonite, 20% rectorite composition.
The preparation method of the present embodiment is comprised the following steps:
A, will natural mineral matter, zirconium oxide, clay mix after add pulverizer in crush, 1/3 al binder is added afterwards, stir It is mixed to form mixture A;
B, addition tridecyl trimethylammonium bromide, absolute ethyl alcohol in mixture A, mixture are added in adding water-bath Heat, at 45 DEG C, constant temperature 30min after heating 45min obtains mixture B to the temperature control of water-bath;
C, 2/3 al binder is added in mixture B, carry out being sufficiently mixed stirring afterwards, until temperature is down to room temperature, Zhi Houjing 2h is put, after then sediment is washed, is dried, then the roasting that heats up obtains thermal cracking catalyst.
In the present embodiment, pulverizer specific breakage rate is 1500 revs/min in step A, and grinding time is 15min.
Embodiment two:
The composition proportion for using for:25 parts of al binder, 35 parts of zirconium oxide, 55 parts of natural mineral matter, 30 parts of clay, tridecyl 30 parts of 20 parts of trimethylammonium bromide, 20 parts of citric acid and absolute ethyl alcohol.
In the present embodiment, natural mineral matter uses 30% kaolin, 20% montmorillonite, 10% diatomite, 10% hydrotalcite, 10% The mixture of bentonite, 20% rectorite composition.
The preparation method of the present embodiment is comprised the following steps:
A, will natural mineral matter, zirconium oxide, clay mix after add pulverizer in crush, 1/3 al binder is added afterwards, stir It is mixed to form mixture A;
B, addition tridecyl trimethylammonium bromide, absolute ethyl alcohol in mixture A, mixture are added in adding water-bath Heat, at 65 DEG C, constant temperature 30min after heating 55min obtains mixture B to the temperature control of water-bath;
C, 2/3 al binder is added in mixture B, carry out being sufficiently mixed stirring afterwards, until temperature is down to room temperature, Zhi Houjing 2h is put, after then sediment is washed, is dried, then the roasting that heats up obtains thermal cracking catalyst.
In the present embodiment, pulverizer specific breakage rate is 3000 revs/min in step A, and grinding time is 35min.
Embodiment three:
The composition proportion for using for:10 parts of al binder, 15 parts of zirconium oxide, 20 parts of natural mineral matter, 15 parts of clay, tridecyl 13 parts of 10 parts of trimethylammonium bromide, 10 parts of citric acid and absolute ethyl alcohol.
In the present embodiment, natural mineral matter uses 30% kaolin, 20% montmorillonite, 10% diatomite, 10% hydrotalcite, 10% The mixture of bentonite, 20% rectorite composition.
The preparation method of the present embodiment is comprised the following steps:
A, will natural mineral matter, zirconium oxide, clay mix after add pulverizer in crush, 1/3 al binder is added afterwards, stir It is mixed to form mixture A;
B, addition tridecyl trimethylammonium bromide, absolute ethyl alcohol in mixture A, mixture are added in adding water-bath Heat, at 50 DEG C, constant temperature 30min after heating 48min obtains mixture B to the temperature control of water-bath;
C, 2/3 al binder is added in mixture B, carry out being sufficiently mixed stirring afterwards, until temperature is down to room temperature, Zhi Houjing 2h is put, after then sediment is washed, is dried, then the roasting that heats up obtains thermal cracking catalyst.
In the present embodiment, pulverizer specific breakage rate is 2000 revs/min in step A, and grinding time is 20min.
Example IV:
The composition proportion for using for:20 parts of al binder, 30 parts of zirconium oxide, 45 parts of natural mineral matter, 25 parts of clay, tridecyl 25 parts of 16 parts of trimethylammonium bromide, 15 parts of citric acid and absolute ethyl alcohol.
In the present embodiment, natural mineral matter uses 30% kaolin, 20% montmorillonite, 10% diatomite, 10% hydrotalcite, 10% The mixture of bentonite, 20% rectorite composition.
The preparation method of the present embodiment is comprised the following steps:
A, will natural mineral matter, zirconium oxide, clay mix after add pulverizer in crush, 1/3 al binder is added afterwards, stir It is mixed to form mixture A;
B, addition tridecyl trimethylammonium bromide, absolute ethyl alcohol in mixture A, mixture are added in adding water-bath Heat, at 60 DEG C, constant temperature 30min after heating 52min obtains mixture B to the temperature control of water-bath;
C, 2/3 al binder is added in mixture B, carry out being sufficiently mixed stirring afterwards, until temperature is down to room temperature, Zhi Houjing 2h is put, after then sediment is washed, is dried, then the roasting that heats up obtains thermal cracking catalyst.
In the present embodiment, pulverizer specific breakage rate is 2500 revs/min in step A, and grinding time is 30min.
Embodiment five:
The composition proportion for using for:15 parts of binding agent, 28 parts of zirconium oxide, 35 parts of natural mineral matter, 20 parts of clay, tridecyl three 20 parts of 15 parts of methyl bromide ammonium, 15 parts of citric acid and absolute ethyl alcohol.
In the present embodiment, natural mineral matter uses 30% kaolin, 20% montmorillonite, 10% diatomite, 10% hydrotalcite, 10% The mixture of bentonite, 20% rectorite composition.
The preparation method of the present embodiment is comprised the following steps:
A, will natural mineral matter, zirconium oxide, clay mix after add pulverizer in crush, 1/3 al binder is added afterwards, stir It is mixed to form mixture A;
B, addition tridecyl trimethylammonium bromide, absolute ethyl alcohol in mixture A, mixture are added in adding water-bath Heat, between 55 DEG C, constant temperature 30min after heating 50min obtains mixture B to the temperature control of water-bath;
C, 2/3 al binder is added in mixture B, carry out being sufficiently mixed stirring afterwards, until temperature is down to room temperature, Zhi Houjing 2h is put, after then sediment is washed, is dried, then the roasting that heats up obtains thermal cracking catalyst.
In the present embodiment, pulverizer specific breakage rate is 2200 revs/min in step A, and grinding time is 25min.
Preparation process is simple of the present invention, preparation process is environment friendly and pollution-free, obtained carbon monoxide-olefin polymeric good stability, can It is effective to improve scrap rubber thermal cracking efficiency, while improve the yield and quality of the oil product that thermal cracking is obtained;In addition, of the invention The preparation method of use is simple to operate, and preparation efficiency is high, can further improve the activity and anti-wear performance of catalyst.
Although an embodiment of the present invention has been shown and described, for the ordinary skill in the art, can be with Understanding can carry out various changes, modification, replacement to these embodiments without departing from the principles and spirit of the present invention And modification, the scope of the present invention be defined by the appended.

Claims (5)

1. a kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric, it is characterised in that:Carbon monoxide-olefin polymeric includes aluminium by weight Binding agent 5-25 parts, zirconium oxide 10-35 parts, natural mineral matter 15-55 parts, clay 10-30 parts, tridecyl trimethylammonium bromide 5-20 parts, citric acid 8-20 parts and absolute ethyl alcohol 10-30 parts.
2. a kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric according to claim 1, it is characterised in that:The natural ore deposit The mixing that material is constituted using 30% kaolin, 20% montmorillonite, 10% diatomite, 10% hydrotalcite, 10% bentonite, 20% rectorite Thing.
3. a kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric according to claim 1, it is characterised in that:It is preferred into Distribution ratio is:15 parts of binding agent, 28 parts of zirconium oxide, 35 parts of natural mineral matter, 20 parts of clay, tridecyl trimethylammonium bromide 15 20 parts of part, 15 parts of citric acid and absolute ethyl alcohol.
4. a kind of preparation method of the scrap rubber thermal cracking carbon monoxide-olefin polymeric described in claim 1 is realized, it is characterised in that: Its preparation method is comprised the following steps:
A, will natural mineral matter, zirconium oxide, clay mix after add pulverizer in crush, 1/3 al binder is added afterwards, stir It is mixed to form mixture A;
B, addition tridecyl trimethylammonium bromide, absolute ethyl alcohol in mixture A, mixture are added in adding water-bath Heat, between 45 DEG C -65 DEG C, constant temperature 30min after heating 45min-55min obtains mixture B to the temperature control of water-bath;
C, 2/3 al binder is added in mixture B, carry out being sufficiently mixed stirring afterwards, until temperature is down to room temperature, Zhi Houjing 2h is put, after then sediment is washed, is dried, then the roasting that heats up obtains thermal cracking catalyst.
5. the preparation method of a kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric according to claim 4, it is characterised in that: Pulverizer specific breakage rate is 1500-3000 revs/min in the step A, and grinding time is 15min-35min.
CN201710261345.6A 2017-04-20 2017-04-20 A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric Withdrawn CN106807347A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710261345.6A CN106807347A (en) 2017-04-20 2017-04-20 A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710261345.6A CN106807347A (en) 2017-04-20 2017-04-20 A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric

Publications (1)

Publication Number Publication Date
CN106807347A true CN106807347A (en) 2017-06-09

Family

ID=59114941

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710261345.6A Withdrawn CN106807347A (en) 2017-04-20 2017-04-20 A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric

Country Status (1)

Country Link
CN (1) CN106807347A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1117517A (en) * 1994-08-24 1996-02-28 中国长江动力公司(集团) Method and equipment for catalytic cracking waste rubber
CN101695666A (en) * 2009-10-26 2010-04-21 重庆市利奇源科技有限公司 Catalyst for pyrolyzing waste rubber and waste plastics to refine oil
CN101898146A (en) * 2009-05-27 2010-12-01 中国石油化工股份有限公司 Catalytic thermal cracking catalyst and preparation method thereof
CN106345444A (en) * 2016-08-28 2017-01-25 山东成泰化工有限公司 Catalyst composition for waste rubber thermocracking

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1117517A (en) * 1994-08-24 1996-02-28 中国长江动力公司(集团) Method and equipment for catalytic cracking waste rubber
CN101898146A (en) * 2009-05-27 2010-12-01 中国石油化工股份有限公司 Catalytic thermal cracking catalyst and preparation method thereof
CN101695666A (en) * 2009-10-26 2010-04-21 重庆市利奇源科技有限公司 Catalyst for pyrolyzing waste rubber and waste plastics to refine oil
CN106345444A (en) * 2016-08-28 2017-01-25 山东成泰化工有限公司 Catalyst composition for waste rubber thermocracking

Similar Documents

Publication Publication Date Title
CN104610768B (en) Asphalt regeneration agent as well as preparation method and application thereof
CN104788975A (en) Asphalt regenerating agent with modification function and preparation method thereof
CN110698023A (en) Method for regulating alkalinity of red mud by pyrolyzing agricultural biomass wastes
CN102585591A (en) Method for making blue offset printing ink
CN106746882A (en) A kind of slag grinding aid
CN107311539A (en) Building waste baking-free brick and preparation method thereof
CN111019365B (en) Method for preparing biological asphalt from lignocellulose biomass hydrothermal carbon
CN104371650B (en) Friction material containing organic nanometer bentonite and preparation method thereof
CN103896543B (en) Baking-free ceramicite taking brown coal germanium tailings as primary raw material and preparation method thereof
CN103964812B (en) Vitrified brick being main raw material with brown coal germanium tailings and preparation method thereof
CN106807347A (en) A kind of scrap rubber thermal cracking carbon monoxide-olefin polymeric
CN103265909A (en) High-solid content quick-drying modified starch lap adhesive and preparation method thereof
CN106345444A (en) Catalyst composition for waste rubber thermocracking
CN103897577B (en) glass coating and preparation method thereof
CN108277055A (en) A kind of biomass charcoal powder densification briquetting fuel preparation method
DE112018000031T5 (en) Process for the preparation of a dilute ceramic additive using epileptic leachate
CN103819174A (en) Sintered ceramsite adopting tailings generated during germanium extraction of lignite as main raw material and preparation method of sintered ceramsite
CN103952203A (en) Comprehensive environment-friendly carbonizing technology by using waste crop straw resources
DE112018000489B4 (en) Production of briquette binder with landfill leachate and its process for the production of industrial briquettes
CN106345445A (en) Catalyst composition for waste plastic thermocracking
CN108587265A (en) A kind of high activity functional form diatom ooze and preparation method thereof
CN103173090A (en) Building coating and preparation process thereof
CN106746840A (en) A kind of cement grinding aid
CN107020151A (en) A kind of Pyrolysis of Plastics Wastes carbon monoxide-olefin polymeric
CN106220766A (en) A kind of butadiene rubber carbon monoxide-olefin polymeric

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
WW01 Invention patent application withdrawn after publication
WW01 Invention patent application withdrawn after publication

Application publication date: 20170609