CN1081217C - Efficient asphalt soaker and its preparation - Google Patents

Efficient asphalt soaker and its preparation Download PDF

Info

Publication number
CN1081217C
CN1081217C CN99102674A CN99102674A CN1081217C CN 1081217 C CN1081217 C CN 1081217C CN 99102674 A CN99102674 A CN 99102674A CN 99102674 A CN99102674 A CN 99102674A CN 1081217 C CN1081217 C CN 1081217C
Authority
CN
China
Prior art keywords
pitch
soaker
asphalt
temperature
durol
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.)
Expired - Fee Related
Application number
CN99102674A
Other languages
Chinese (zh)
Other versions
CN1270981A (en
Inventor
刘朗
智林杰
宋进仁
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.)
Shanxi Institute of Coal Chemistry of CAS
Original Assignee
Shanxi Institute of Coal Chemistry of CAS
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 Shanxi Institute of Coal Chemistry of CAS filed Critical Shanxi Institute of Coal Chemistry of CAS
Priority to CN99102674A priority Critical patent/CN1081217C/en
Publication of CN1270981A publication Critical patent/CN1270981A/en
Application granted granted Critical
Publication of CN1081217C publication Critical patent/CN1081217C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

The present invention relates to a high-efficient asphalt soaker and a preparation method thereof. The asphalt soaker is prepared from coal tar pitch or petroleum pitch which is used as base material, and 5 to 15% of durene as additive by the method of pressurized chemical copolymerization. The asphalt soaker has softening point of 100 to 150 DEG C, carbon yield of 60 to 72% and viscosity number at 300 DEG C lower than 0.12 Pa.s.

Description

A kind of efficient asphalt soaker and preparation method thereof
The invention belongs to the preparation method of efficient asphalt soaker, relate in particular to the preparation method of a kind of low viscosity, high carbon yield pitch soaker.
Asphalt impregnant is the density strengthening agent of raw material of wood-charcoal material and goods thereof, and its products obtained therefrom is widely used in fields such as electronics, metallurgy, machinery, space flight, aviation.In the production of carbon material, especially in the preparation process of c/c matrix material, the quality quality of asphalt impregnant directly has influence on the performance and the production cost of product.A kind of Perfected process that makes pitch have low viscosity and high charcoal yield is to optimize the bituminous molecular structure, makes its size to fit, is evenly distributed.Many for this reason scholars propose to prepare pitch to optimize its molecular structure from pure compound through catalyzed polymerization.But owing to adopt pure compound, production cost is increased substantially, simultaneously, this method also has operational path longer, severe reaction conditions, shortcomings such as catalyst separating difficulty.As Eur.Pat.Appl.EP381493, from naphthalene preparation bituminous process, with AlCl 3Be catalyzer, after reaction, need to separate AlCl through four above steps 3, and be difficult to separate clean.For another example, Jpn.KoKai Tokkyo Koho JP04154888 by the simple hydrocarbon polymer preparation pitch that sets out, adopts to have corrosive super acids HF/BF 3Be catalyzer, bring inconvenience to equipment design and production operation.For avoiding these deficiencies, people have developed the molecular structure that the normal pressure chemical copolymerization method improves dipping agent bitumen.Thereby so-called normal pressure chemical copolymerization method promptly adds the purpose that the chemical substance warp with a fixed structure reaches adjustment with the copolymerization of asphaltene molecule normal pressure, optimizes the asphaltene molecule structure in tar or pitch.As Jpn.Kokai Tokkyo Koho JP03103490, in coal tar, add some simple organics and obtain 78.6 ℃ of softening temperatures, the dipping agent bitumen of fixed carbon content 32.7% through the normal pressure heat treated.But this type of dipping agent bitumen charcoal yield is lower, and purposes is limited.Especially in special dimensions such as aerospace, because the singularity (as High Temperature High Pressure) and the expensive characteristic of its material produce technological process, performance to dipping agent bitumen also has higher requirement (will get well as temperature flowing, preferably less than 0.15Pa.s, the charcoal yield is more preferably greater than 65% at 300 ℃ viscosity numbers).Add the requirement that pitch that some simple organism adopt normal pressure chemical copolymerization methods to make is difficult to satisfy special dimensions such as aerospace like this.
The purpose of this invention is to provide efficient asphalt soaker of a kind of low viscosity high yield charcoal and preparation method thereof.
The object of the present invention is achieved like this, adopts the pressurization chemical copolymerization to obtain good fluidity, asphalt impregnant that charcoal yield is high with coal-tar pitch or the petroleum pitch durol that is raw material through adding 5-15%.
Made efficient asphalt soaker, its softening temperature are 100-150 ℃, charcoal yield 60.0%-72.0%, and 300 ℃ viscosity number is less than 0.12Pa.s.
Preparation method of the present invention is as follows:
(1) durol of interpolation 5-15% in material asphalt mixes;
(2) blended is packed in the reactor, feed nitrogen protection, sealed reactor rises to 380-440 ℃ temperature with the heat-up rate of 3-5 ℃/min;
(3) stirring was reacted 6-28 hour under 380-440 ℃ of temperature and certain pressure down;
(4) go out still behind the naturally cooling, get high-quality dipping pitch.
Aforesaid pressure is 0.6-2.5Mp.
Aforesaid pitch is medium temperature coal pitch, petroleum pitch.
Aforesaid additive also can be other additive with the durol structural similitude.
Aforesaid pressure is provided by reaction system self or the external world provides.
The final performance of the made bituminous of the present invention can require to control by reaction times, temperature of reaction, reaction pressure according to difference.
The present invention has following advantage:
(1) raw material sources are extensive, low price.
(2) technological process is simple, and energy consumption is low, saves time, and is laborsaving.
(3) can artificially control the performance of product, to satisfy the needs of different levels.
(4) excellent product quality, stable performance.
Most preferred embodiment of the present invention is as follows:
Embodiment 1
Take by weighing 90.0g medium temperature coal pitch (S.P.:68 ℃ C.Y.:43.01%) is mixed in the reactor of packing into nitrogen protection with the 10.0g durol; sealed reactor rises to 430 ℃ of constant temperature, stirring reaction 6h with the temperature rise rate of 4 ℃/min; system pressure 1.0Mp; reaction finishes the back naturally cooling, goes out still, gets high-quality dipping pitch 80.0g; S.P.:100 ℃; C.Y.:59.54%, and viscosity (300 ℃, 20r/min): 0.035Pa.s.
Embodiment 2
Take by weighing 90.0g medium temperature coal pitch (S.P.:68 ℃ C.Y.:43.01%) is mixed in the reactor of packing into nitrogen protection with the 10.0g durol; sealed reactor rises to 420 ℃ of constant temperature, stirring reaction 12h with the temperature rise rate of 4 ℃/min; system pressure 0.6Mp; reaction finishes the back naturally cooling, goes out still, gets high-quality dipping pitch 65.0g; S.P.:130 ℃; C.Y.:68.02%, and viscosity (300 ℃, 20r/min): 0.074Pa.s.
Embodiment 3
Take by weighing 95.0g medium temperature coal pitch (S.P.:68 ℃ C.Y.:43.01%) is mixed in the reactor of packing into nitrogen protection with the 5.0g durol; sealed reactor rises to 420 ℃ of constant temperature, stirring reaction 12h with the temperature rise rate of 4 ℃/min; system pressure 0.8Mp; reaction finishes the back naturally cooling, goes out still, gets high-quality dipping pitch 60.0g; S.P.:146 ℃; C.Y.:72.15%, and viscosity (300 ℃, 20r/min): 0.120Pa.s.
Embodiment 4
Take by weighing 85.0g medium temperature coal pitch (S.P.:68 ℃ C.Y.:43.01%) is mixed in the reactor of packing into nitrogen protection with the 15.0g durol; sealed reactor rises to 420 ℃ of constant temperature, stirring reaction 12h with the temperature rise rate of 4 ℃/min; system pressure 0.8Mp; reaction finishes the back naturally cooling, goes out still, gets high-quality dipping pitch 75.0g; S.P.:118 ℃; C.Y.:62.07%, and viscosity (300 ℃, 20r/min): 0.042Pa.s.
Embodiment 5
Take by weighing 90.0g medium temperature coal pitch (S.P.:68 ℃ C.Y.:43.01%) is mixed in the reactor of packing into nitrogen protection with the 10.0g durol; sealed reactor rises to 410 ℃ of constant temperature, stirring reaction 28h with the temperature rise rate of 3 ℃/min; system pressure 2.5Mp; reaction finishes the back naturally cooling, goes out still, gets high-quality dipping pitch 70.0g; S.P.:106 ℃; C.Y.:66.67%, and viscosity (300 ℃, 20r/min): 0.070Pa.s.
Embodiment 6
Take by weighing 90.0g medium temperature coal pitch (S.P.:68 ℃ C.Y.:43.01%) is mixed in the reactor of packing into nitrogen protection with the 10.0g durol; sealed reactor rises to 440 ℃ of constant temperature, stirring reaction 6h with the temperature rise rate of 5 ℃/min; system pressure 1.2Mp; reaction finishes the back naturally cooling, goes out still, gets high-quality dipping pitch 70.0g; S.P.:120 ℃; C.Y.:63.12%, and viscosity (300 ℃, 20r/min): 0.045Pa.s.
Embodiment 7
Take by weighing 90.0g petroleum pitch (S.P.:65 ℃ C.Y.:40.12%) is mixed in the reactor of packing into nitrogen protection with the 10.0g durol; sealed reactor rises to 380 ℃ of constant temperature, stirring reaction 20h with the temperature rise rate of 3 ℃/min; system pressure 0.8Mp; reaction finishes the back naturally cooling, goes out still, gets high-quality dipping pitch 70.0g; S.P.:121 ℃; C.Y.:64.58%, and viscosity (300 ℃, 20r/min): 0.052Pa.s.

Claims (2)

1. an efficient asphalt soaker adopts the pressurization chemical copolymerization method to make, and it is characterized in that with coal-tar pitch or petroleum pitch be raw material, add the durol of 5-15%, the softening temperature of product soaker is 100-150 ℃, and the charcoal yield is 60-72%, and 300 ℃ viscosity number is less than 0.12Pa.s.
2. method for preparing the described asphalt impregnant of claim 1 is characterized in that:
(1) durol of interpolation 5-15% in material asphalt mixes;
(2) compound is packed in the reactor, feed nitrogen protection, sealed reactor rises to 380-440 ℃ temperature with the heat-up rate of 3-5 ℃/min;
(3) stirring was reacted 6-28 hour under 380-440 ℃ of temperature and 0.6-2.5MPa down;
(4) go out still behind the naturally cooling, get high-quality dipping pitch.
CN99102674A 1999-04-15 1999-04-15 Efficient asphalt soaker and its preparation Expired - Fee Related CN1081217C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN99102674A CN1081217C (en) 1999-04-15 1999-04-15 Efficient asphalt soaker and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN99102674A CN1081217C (en) 1999-04-15 1999-04-15 Efficient asphalt soaker and its preparation

Publications (2)

Publication Number Publication Date
CN1270981A CN1270981A (en) 2000-10-25
CN1081217C true CN1081217C (en) 2002-03-20

Family

ID=5270925

Family Applications (1)

Application Number Title Priority Date Filing Date
CN99102674A Expired - Fee Related CN1081217C (en) 1999-04-15 1999-04-15 Efficient asphalt soaker and its preparation

Country Status (1)

Country Link
CN (1) CN1081217C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101289625B (en) * 2008-06-03 2010-12-15 山西宏特煤化工有限公司 Production process of dipping agent bitumen
CN101987968A (en) * 2010-11-29 2011-03-23 同济大学 Method for coal tar pitch hydrocracking lightening reaction technology
CN111725478B (en) * 2020-06-29 2023-02-24 辽宁红德电碳制品有限公司 Impregnation process for carbon strip production

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1110693A (en) * 1995-01-13 1995-10-25 范运洪 Modified asphaltum additives and its production technology

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1110693A (en) * 1995-01-13 1995-10-25 范运洪 Modified asphaltum additives and its production technology

Also Published As

Publication number Publication date
CN1270981A (en) 2000-10-25

Similar Documents

Publication Publication Date Title
CN104959154A (en) Catalyst for preparing levulinate ester and method for preparing levulinate ester by using catalyst
CN1081217C (en) Efficient asphalt soaker and its preparation
CN1887832A (en) Large scale synthesis process of carbon fluorides
CN1262304A (en) Process for preparing asphalt impregnant by pressurized heat treatment
CN1048955C (en) Method for producing activated carbon with high specific surface area from asphalt
CN202989064U (en) Special device for preparing high-purity aromatic asphalt
CN1944359A (en) Process for preparing 2,5-norbornadiene
CN1022240C (en) Process for producing perfluoro-carbonyl fluoride
CN114805755B (en) Super light color high stability hydrogenated terpene phenol resin and preparation method thereof
CN106944110A (en) A kind of hydrogen chloride synthesis vinyl chloride thereof catalyst without mercury and preparation method
CN1151060C (en) Process for preparing intermediate-phase carbon microspheres
CN1362461A (en) Polyamide thermosol
CN1053801A (en) Continuous processing is produced the method for the polymkeric substance of carbon monoxide and one or more alefinically unsaturated compounds
CN1285389A (en) Method for increasing soluble composition of toluene insoluble pyridine in asphalt
CN1179992C (en) Prep. of high softening point and high fusion viscosity pentadiene petroleum resin
CN1272453A (en) Preparation method of mesophase carbon microsphere
CN107540499B (en) Method for maintaining high aromatic selectivity in process of preparing aromatic hydrocarbon from methanol
CN1736996A (en) A kind of novel method of producing methyl hexahydrophthalic anhydride
EP3527559B1 (en) Gamma-butyrolactone composition and method for producing same
CN115746896B (en) Synthesis method of alkane bio-based lubricating oil base oil
CN1036466C (en) Inorganic modified paint of coal tar and preparing process
CN1232584C (en) Method of preparing zirconium containing asphalt using zirconium oxychloride
CN101768143B (en) Method for producing hexahydrophthalic anhydride by using C4 mixture
CN1216024C (en) Preparing-1-pentanal from mixed solvent ion liquid of tetrafluorborate methyl buty I imidazole salt/water
CN114874079B (en) Method for preparing bio-based 2, 5-hexanedione by taking cellulose as raw material

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee