CN110028253A - A kind of high-performance cement and preparation method thereof - Google Patents

A kind of high-performance cement and preparation method thereof Download PDF

Info

Publication number
CN110028253A
CN110028253A CN201910301251.6A CN201910301251A CN110028253A CN 110028253 A CN110028253 A CN 110028253A CN 201910301251 A CN201910301251 A CN 201910301251A CN 110028253 A CN110028253 A CN 110028253A
Authority
CN
China
Prior art keywords
parts
amino
cement
performance
performance cement
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Withdrawn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
CN201910301251.6A
Other languages
Chinese (zh)
Inventor
梁剑
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CN201910301251.6A priority Critical patent/CN110028253A/en
Publication of CN110028253A publication Critical patent/CN110028253A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B40/00Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
    • C04B40/0028Aspects relating to the mixing step of the mortar preparation
    • C04B40/0039Premixtures of ingredients
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B7/00Hydraulic cements
    • C04B7/02Portland cement

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

The invention discloses a kind of high-performance cements, it is characterised in that it includes the raw material of following parts by weight: 50-70 parts of Portland clinker, 5-10 parts of solonchak, 5-10 parts of agstone, 3-8 parts of attapulgite, 3-7 parts of coal dust, 5-10 parts of nanometer boron fibre, 1-5 parts of vermiculite, 0.3-0.8 parts of urobilin hydrochloride, bis- (2- amino-ethyl ether) 0.5-1 parts of the tetraacethyl fluosilicates of 2- chloroethyl urea ionization ethylene glycol, 0.5-1.5 parts of cement additive.The invention also discloses the preparation methods of the high-performance cement.High-performance cement disclosed by the invention has that compression strength and early strength are high, production cost is low, setting time is short, lubricity etc. is had excellent performance, and unit-hour output and stability are high, and powder grinds the good advantage of effect.

Description

A kind of high-performance cement and preparation method thereof
Technical field
The present invention relates to building material technical fields more particularly to a kind of high-performance cement and preparation method thereof.
Background technique
Cement be current mankind production and life must one of inseparable construction material, it has sufficient raw, at This is low, and easy for construction, durability is good, easy to maintain to wait remarkable advantages, is widely used in the engineerings such as civil construction, water conservancy, national defence, It is most widely used as the mankind, a kind of maximum construction material of usage amount.The quality of its performance directly determines the height of construction quality Low, therefore, the high performance cement of demand becomes at this stage focus of attention in the industry.
Cement is a kind of powdery hydraulicity inorganic coagulation material, at slurry after adding water and stirring, can harden in air or Person is preferably hardened in water, and can the materials such as sand, stone are cemented together securely.There are many type of cement, by its purposes General-purpose cement, cement special and characteristic cement three categories can be divided into performance.But either general-purpose cement, dedicated on the market at present Cement or characteristic cement in the production process, coal consumption and material consumption the problem of it is very serious, higher cost is made, in addition generally deposits High in the getting up early heat of hydration, setting time is resolute, and later strength has the problems such as different degrees of retraction.
It is to improve and realize the effective way of various characteristics that cement additive is added in cement.It can accelerate cement dry and hard Intensity or reduction cement water consumption after speed, raising cement are dry and hard, it can also improve concrete scroll and excite each mixing The hydration activity of material, and then cement early strength and later strength are improved, therefore, cement addition is added in cement production process Agent is necessary.But cement additive in the prior art has a single function, it is not high to the improvement degree of cement comprehensive performance.
Chinese patent literature CN201610722399.3 discloses a kind of cement formula, it is characterised in that: by following weight The raw material composition of part: 20-40 parts of clinker, 10-20 parts of lime stone, 10-30 parts of carbide slag, 5-10 parts of slag, anhydrous gypsum 10-20 parts, 1-10 parts of pigment, 10-20 parts of fluorgypsum, 10-30 parts of lime-ash, 10-30 parts of sandstone, 12-15 parts of manganese slag.Formula benefit The cement manufactured with industrial waste material, formula is scientific and reasonable, effectively reduces cement manufacturing cost, while utilizing waste system Cement is made, is improved the ecological environment, environmental protection concept is met.But this cement setting time is longer, compression strength and early strength Need to be further increased.
Therefore, the height that a kind of compression strength and early strength are high, production cost is low, setting time is short, stability is high is developed Performance cement accords with the demands of the market, and has very important significance.
Summary of the invention
In order to overcome the defects of the prior art, the present invention is intended to provide a kind of high-performance cement and preparation method thereof, is somebody's turn to do Preparation method is simple, and raw material sources are abundant, and price is less expensive, of less demanding to equipment and reaction condition, is suitble to scale Production has biggish application value;There is compression strength by the high-performance cement that this preparation method is prepared With early strength is high, production cost is low, setting time is short, lubricity etc. is had excellent performance, unit-hour output and stability are high, powder mill The good advantage of effect.
The present invention is realized by the following scheme:
A kind of high-performance cement, the raw material including following parts by weight: 50-70 parts of Portland clinker, 5-10 parts of solonchak, 5-10 parts of agstone, 3-8 parts of attapulgite, 3-7 parts of coal dust, 5-10 parts of nanometer boron fibre, 1-5 parts of vermiculite, urobilin hydrochloric acid 0.3-0.8 parts of salt, 2- chloroethyl urea ionize ethylene glycol bis- (2- amino-ethyl ether) 0.5-1 parts of tetraacethyl fluosilicates, water 0.5-1.5 parts of mud additive.
Further, the cement additive is made by milling after mixing of the component of following parts by weight: 4,8- Dioxy-dodecane -1,12- diamines and 1,30-40 parts of glycerol condensation polymer of 3- diglycidyl ether, Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3), 4- ammonia Two lithium (No. CAS: 71231-14-6) copolymer 25-30 of base-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid Part.
Preferably, 4,8- dioxy-dodecane -1,12- diamines and 1, the system of 3- diglycidyl ether glycerol condensation polymer Preparation Method includes the following steps: 4,8- dioxy-dodecane -1,12- diamines, 1,3- diglycidyl ether glycerol being added to two In first sulfoxide, it is stirred to react at 70-80 DEG C 8-10 hours, dimethyl sulfoxide is evaporated off in back spin.
Preferably, 4,8- dioxy-dodecane -1,12- diamines, 1,3- diglycidyl ether glycerol, dimethyl sulfoxide Mass ratio is 1:1:(3-5).
Preferably, the Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) urine Glycosides 5'- phosplate (No. CAS: 97950-37-3), 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- two The preparation method of two lithium of sulfonic acid (No. CAS: 71231-14-6) copolymer, include the following steps: by Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3), 4- ammonia Two lithium (No. CAS: 71231-14-6) of base-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid is added to organic In solvent, then initiator is added thereto, is stirred to react under nitrogen or atmosphere of inert gases 6-8 hours, back spin has been evaporated off Solvent.
Preferably, the initiator is selected from least one of azodiisobutyronitrile, azobisisoheptonitrile;It is described organic molten Agent is selected from least one of tetrahydrofuran, DMAC N,N' dimethyl acetamide, N-Methyl pyrrolidone;The inert gas is selected from helium One of gas, neon, argon gas.
Preferably, the Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) urine Glycosides 5'- phosplate (No. CAS: 97950-37-3), 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- two Two lithium of sulfonic acid (No. CAS: 71231-14-6), organic solvent, initiator mass ratio be 2:1:0.5:(10-15): (0.01- 0.03)。
Further, the 2- chloroethyl urea ionizes bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol Preparation method includes the following steps: bis- (the 2- amino-ethyl ether) tetraacethyls of 2- chloroethyl urea, ethylene glycol being added to acetone In, it is stirred to react at 40-60 DEG C 6-8 hours, acetone is evaporated off in back spin, then it is 10-20% that product, which is added to mass fraction, Prodan aqueous solution in, be stirred to react at 50-60 DEG C 10-14 hours, water is evaporated off in back spin.
Preferably, the 2- chloroethyl urea, ethylene glycol bis- (2- amino-ethyl ether) tetraacethyls, acetone, prodan The mass ratio of aqueous solution is 1:1.55:(10-15): (10-20).
Further, the preparation method of the high-performance cement includes the following steps: to mix each raw material according to parts by weight Match, intergrinding to specific surface area is 200-300m2/ kg, obtains high-performance cement.
The beneficial effects of adopting the technical scheme are that
(1) high-performance cement provided by the invention, preparation method is simple, and raw material sources are abundant, and price is less expensive, right Equipment and reaction condition are of less demanding, are suitble to large-scale production, have biggish application value.
(2) high-performance cement provided by the invention, have compression strength and early strength are high, production cost is low, condensation when Between short, lubricity etc. have excellent performance, unit-hour output and stability are high, and powder grinds the good advantage of effect.
(3) high-performance cement provided by the invention adds solonchak, manufactures cement using waste, improves the ecological environment, accords with Close environmental protection concept;Tetraacethyl fluosilicate is dissolved in water to dissociate for 2- chloroethyl urea ionization ethylene glycol bis- (2- amino-ethyl ethers) Fluosilicic acid radical ion and bis- (2- amino-ethyl ether) the tetraacethyl cations of 2- chloroethyl urea ionization ethylene glycol out, in cement Grain surface forms oriented attachment, generates absorption peptizaiton and lubricating action to cement granules, is conducive to cement granules floccule body Disintegration, thus have diminishing plastication, and act synergistically with urobilin hydrochloride, play the role of Absorptive complex wave, reduction solonchak Middle harmful metal ion is influenced caused by environment.
(4) high-performance cement provided by the invention, each materials compatibility is good, and synergistic effect forms network structure, nanometer boron Fiber can be embedded, and increase the intensity of cement, prevent the cracking of cement, the addition of nano material, in cement hydration process Middle package ion forms protective film, solid cement concrete hydrating micro-structure, to improve low-heat silicate water in cement surface The early strength of mud, and effectively absorption, curing of chloride ion and sulfate ion, hinder chloride ion and sulfate diffusivity, from And plays the role of improving the quality of cement and prolong its service life.
(5) high-performance cement provided by the invention, adds additive, group containing different activities, and synergistic effect improves cement Grinding-aid effect in grinding process, so that more densification in cement slurry stirring, condensation hardening process, promotes water cement early period Change, can also promote further hydration, improve the performance of cement.
Specific embodiment
In order to make those skilled in the art more fully understand technical solution of the present invention, and make features described above of the invention, Purpose and advantage are more clear understandable, and the present invention will be further explained with reference to the examples below.Embodiment is only used for It is bright the present invention rather than limit the scope of the invention.
Raw material described in the following embodiments of the present invention is both from commercially available.
Embodiment 1
A kind of high-performance cement, the raw material including following parts by weight: 50 parts of Portland clinker, 5 parts of solonchak, lime stone 5 parts of powder, 3 parts of attapulgite, 5 parts of 3 part, nanometer boron fibre of coal dust, 1 part of vermiculite, 0.3 part of urobilin hydrochloride, 2- chloroethyl urine Bis- (2- amino-ethyl ether) 0.5 part of the tetraacethyl fluosilicates of element ionization ethylene glycol, 0.5 part of cement additive.
The cement additive is made by milling after mixing of the component of following parts by weight: 4,8- dioxy-ten two Alkane -1,12- diamines and 1,30 parts of condensation polymer of 3- diglycidyl ether glycerol, Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3), 4- amino-N- [3- (ethylene Base sulphonyl) phenyl] two 25 parts of copolymer of lithium (No. CAS: 71231-14-6) of naphthalimide -3,6- disulfonic acid.
4,8- dioxy-dodecane -1,12- diamines and 1, the preparation method of 3- diglycidyl ether glycerol condensation polymer, Include the following steps: 4,8- dioxy-dodecane -1,12- diamines 1kg, 1,3- diglycidyl ether glycerol 1kg being added to diformazan In sulfoxide 3kg, it is stirred to react at 70 DEG C 8 hours, dimethyl sulfoxide is evaporated off in back spin.
The Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- are mono- Phosphate (No. CAS: 97950-37-3), two lithium of 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid The preparation method of (No. CAS: 71231-14-6) copolymer includes the following steps: Ginsenoside F2 (No. CAS: 62025-49- 4) 2kg, 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3) 1kg, 4- amino - Two lithium (No. CAS: 71231-14-6) 0.5kg of N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid is added to four In hydrogen furans 10kg, then azodiisobutyronitrile 0.01kg is added thereto, is stirred to react under nitrogen atmosphere 6 hours, it is rear to rotate Remove tetrahydrofuran.
The preparation method of 2- chloroethyl urea ionization bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol, Include the following steps: bis- (2- amino-ethyl ether) the tetraacethyl 1.55kg of 2- chloroethyl urea 1kg, ethylene glycol being added to acetone It in 10kg, is stirred to react at 40 DEG C 6 hours, acetone is evaporated off in back spin, then product is added to the fluorine that mass fraction is 10% In the aqueous solution 10kg of sodium metasilicate, it is stirred to react at 50 DEG C 10 hours, water is evaporated off in back spin.
The preparation method of the high-performance cement includes the following steps: each raw material according to parts by weight mixture, intergrinding It is 200m to specific surface area2/ kg, obtains high-performance cement.
Embodiment 2
A kind of high-performance cement, the raw material including following parts by weight: 55 parts of Portland clinker, 6.5 parts of solonchak, lime 6.5 parts of mountain flour, 4.5 parts of attapulgite, 6.5 parts of 4.5 part, nanometer boron fibre of coal dust, 2.5 parts of vermiculite, urobilin hydrochloride 0.45 Part, 2- chloroethyl urea ionize ethylene glycol bis- (2- amino-ethyl ether) 0.65 part of tetraacethyl fluosilicates, cement additive 0.7 Part.
The cement additive is made by milling after mixing of the component of following parts by weight: 4,8- dioxy-ten two Alkane -1,12- diamines and 1,33 parts of condensation polymer of 3- diglycidyl ether glycerol, Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3), 4- amino-N- [3- (ethylene Base sulphonyl) phenyl] two 27 parts of copolymer of lithium (No. CAS: 71231-14-6) of naphthalimide -3,6- disulfonic acid.
4,8- dioxy-dodecane -1,12- diamines and 1, the preparation method of 3- diglycidyl ether glycerol condensation polymer, Include the following steps: 4,8- dioxy-dodecane -1,12- diamines 1kg, 1,3- diglycidyl ether glycerol 1kg being added to diformazan In sulfoxide 3.5kg, it is stirred to react at 73 DEG C 8.5 hours, dimethyl sulfoxide is evaporated off in back spin.
The Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- are mono- Phosphate (No. CAS: 97950-37-3), two lithium of 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid The preparation method of (No. CAS: 71231-14-6) copolymer includes the following steps: Ginsenoside F2 (No. CAS: 62025-49- 4) 2kg, 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3) 1kg, 4- amino - Two lithium (No. CAS: 71231-14-6) 0.5kg of N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid is added to N, In N- dimethyl acetamide 12kg, then azobisisoheptonitrile 0.015kg is added thereto, is stirred to react 6.5 under helium atmosphere Hour, n,N-dimethylacetamide is evaporated off in back spin.
The preparation method of 2- chloroethyl urea ionization bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol, Include the following steps: bis- (2- amino-ethyl ether) the tetraacethyl 1.55kg of 2- chloroethyl urea 1kg, ethylene glycol being added to acetone It in 11.5kg, is stirred to react at 45 DEG C 6.5 hours, acetone is evaporated off in back spin, then it is 13% that product, which is added to mass fraction, Prodan aqueous solution 13kg in, be stirred to react at 53 DEG C 11.5 hours, water is evaporated off in back spin.
The preparation method of the high-performance cement includes the following steps: each raw material according to parts by weight mixture, intergrinding It is 230m to specific surface area2/ kg, obtains high-performance cement.
Embodiment 3
A kind of high-performance cement, the raw material including following parts by weight: 60 parts of Portland clinker, 7.5 parts of solonchak, lime 7 parts of mountain flour, 6 parts of attapulgite, 7 parts of 5 part, nanometer boron fibre of coal dust, 3 parts of vermiculite, 0.5 part of urobilin hydrochloride, 2- chloroethyl Urea ionizes bis- (2- amino-ethyl ether) 0.8 part of the tetraacethyl fluosilicates of ethylene glycol, 0.9 part of cement additive.
The cement additive is made by milling after mixing of the component of following parts by weight: 4,8- dioxy-ten two Alkane -1,12- diamines and 1,35 parts of condensation polymer of 3- diglycidyl ether glycerol, Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3), 4- amino-N- [3- (ethylene Base sulphonyl) phenyl] two 27 parts of copolymer of lithium (No. CAS: 71231-14-6) of naphthalimide -3,6- disulfonic acid.
4,8- dioxy-dodecane -1,12- diamines and 1, the preparation method of 3- diglycidyl ether glycerol condensation polymer, Include the following steps: 4,8- dioxy-dodecane -1,12- diamines 1kg, 1,3- diglycidyl ether glycerol 1kg being added to diformazan In sulfoxide 4kg, it is stirred to react at 75 DEG C 9 hours, dimethyl sulfoxide is evaporated off in back spin.
The Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- are mono- Phosphate (No. CAS: 97950-37-3), two lithium of 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid The preparation method of (No. CAS: 71231-14-6) copolymer includes the following steps: Ginsenoside F2 (No. CAS: 62025-49- 4) 2kg, 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3) 1kg, 4- amino - Two lithium (No. CAS: 71231-14-6) 0.5kg of N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid is added to N- In methyl pyrrolidone 12.5kg, then azodiisobutyronitrile 0.02kg is added thereto, it is small to be stirred to react 7 under neon atmosphere When, N-Methyl pyrrolidone is evaporated off in back spin.
The preparation method of 2- chloroethyl urea ionization bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol, Include the following steps: bis- (2- amino-ethyl ether) the tetraacethyl 1.55kg of 2- chloroethyl urea 1kg, ethylene glycol being added to acetone It in 13kg, is stirred to react at 50 DEG C 7 hours, acetone is evaporated off in back spin, then product is added to the fluorine that mass fraction is 15% In the aqueous solution 15kg of sodium metasilicate, it is stirred to react at 55 DEG C 12 hours, water is evaporated off in back spin.
The preparation method of the high-performance cement includes the following steps: each raw material according to parts by weight mixture, intergrinding It is 250m to specific surface area2/ kg, obtains high-performance cement.
Embodiment 4
A kind of high-performance cement, the raw material including following parts by weight: 65 parts of Portland clinker, 9 parts of solonchak, lime stone 9 parts of powder, 7 parts of attapulgite, 9 parts of 6 part, nanometer boron fibre of coal dust, 4 parts of vermiculite, 0.7 part of urobilin hydrochloride, 2- chloroethyl urine Bis- (2- amino-ethyl ether) 0.9 part of the tetraacethyl fluosilicates of element ionization ethylene glycol, 1.4 parts of cement additive.
The cement additive is made by milling after mixing of the component of following parts by weight: 4,8- dioxy-ten two Alkane -1,12- diamines and 1,38 parts of condensation polymer of 3- diglycidyl ether glycerol, Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3), 4- amino-N- [3- (ethylene Base sulphonyl) phenyl] two 29 parts of copolymer of lithium (No. CAS: 71231-14-6) of naphthalimide -3,6- disulfonic acid.
4,8- dioxy-dodecane -1,12- diamines and 1, the preparation method of 3- diglycidyl ether glycerol condensation polymer, Include the following steps: 4,8- dioxy-dodecane -1,12- diamines 1kg, 1,3- diglycidyl ether glycerol 1kg being added to diformazan In sulfoxide 4.5kg, it is stirred to react at 78 DEG C 9.5 hours, dimethyl sulfoxide is evaporated off in back spin.
The Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- are mono- Phosphate (No. CAS: 97950-37-3), two lithium of 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid The preparation method of (No. CAS: 71231-14-6) copolymer includes the following steps: Ginsenoside F2 (No. CAS: 62025-49- 4) 2kg, 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3) 1kg, 4- amino - Two lithium (No. CAS: 71231-14-6) 0.5kg of N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid has been added to In solvent 14.5kg, then initiator 0.025kg is added thereto, is stirred to react under argon atmosphere 7.5 hours, back spin is evaporated off Remove organic solvent;The initiator is that azodiisobutyronitrile, azobisisoheptonitrile 3:5 in mass ratio are mixed;It is described Organic solvent is that tetrahydrofuran, DMAC N,N' dimethyl acetamide, N-Methyl pyrrolidone 1:3:5 in mass ratio are mixed.
The preparation method of 2- chloroethyl urea ionization bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol, Include the following steps: bis- (2- amino-ethyl ether) the tetraacethyl 1.55kg of 2- chloroethyl urea 1kg, ethylene glycol being added to acetone It in 14.5kg, is stirred to react at 55 DEG C 7.5 hours, acetone is evaporated off in back spin, then it is 19% that product, which is added to mass fraction, Prodan aqueous solution 19kg in, be stirred to react at 58 DEG C 13.5 hours, water is evaporated off in back spin.
The preparation method of the high-performance cement includes the following steps: each raw material according to parts by weight mixture, intergrinding It is 290m to specific surface area2/ kg, obtains high-performance cement.
Embodiment 5
A kind of high-performance cement, the raw material including following parts by weight: 70 parts of Portland clinker, 10 parts of solonchak, lime 10 parts of mountain flour, 8 parts of attapulgite, 10 parts of 7 part, nanometer boron fibre of coal dust, 5 parts of vermiculite, 0.8 part of urobilin hydrochloride, 2- chloroethene Base urea ionizes bis- (2- amino-ethyl ether) 1 part of the tetraacethyl fluosilicates of ethylene glycol, 1.5 parts of cement additive.
The cement additive is made by milling after mixing of the component of following parts by weight: 4,8- dioxy-ten two Alkane -1,12- diamines and 1,40 parts of condensation polymer of 3- diglycidyl ether glycerol, Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3), 4- amino-N- [3- (ethylene Base sulphonyl) phenyl] two 30 parts of copolymer of lithium (No. CAS: 71231-14-6) of naphthalimide -3,6- disulfonic acid.
4,8- dioxy-dodecane -1,12- diamines and 1, the preparation method of 3- diglycidyl ether glycerol condensation polymer, Include the following steps: 4,8- dioxy-dodecane -1,12- diamines 1kg, 1,3- diglycidyl ether glycerol 1kg being added to diformazan In sulfoxide 5kg, it is stirred to react at 80 DEG C 10 hours, dimethyl sulfoxide is evaporated off in back spin.
The Ginsenoside F2 (No. CAS: 62025-49-4), 5- (N- biotinyl -3- aminoallyl) uridine 5'- are mono- Phosphate (No. CAS: 97950-37-3), two lithium of 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid The preparation method of (No. CAS: 71231-14-6) copolymer includes the following steps: Ginsenoside F2 (No. CAS: 62025-49- 4) 2kg, 5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate (No. CAS: 97950-37-3) 1kg, 4- amino - Two lithium (No. CAS: 71231-14-6) 0.5kg of N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid is added to four In hydrogen furans 15kg, then azodiisobutyronitrile 0.03kg is added thereto, is stirred to react under nitrogen atmosphere 8 hours, it is rear to rotate Remove tetrahydrofuran.
The preparation method of 2- chloroethyl urea ionization bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol, Include the following steps: bis- (2- amino-ethyl ether) the tetraacethyl 1.55kg of 2- chloroethyl urea 1kg, ethylene glycol being added to acetone It in 15kg, is stirred to react at 60 DEG C 8 hours, acetone is evaporated off in back spin, then product is added to the fluorine that mass fraction is 20% In the aqueous solution 20kg of sodium metasilicate, it is stirred to react at 60 DEG C 14 hours, water is evaporated off in back spin.
The preparation method of the high-performance cement includes the following steps: each raw material according to parts by weight mixture, intergrinding It is 300m to specific surface area2/ kg, obtains high-performance cement.
Comparative example 1
Commercially available portland cement.
Comparative example 2
This example provides a kind of cement, and preparation method and formula are substantially the same manner as Example 1, the difference is that without addition coal Powder.
Comparative example 3
This example provides a kind of cement, and preparation method and formula are substantially the same manner as Example 1, the difference is that without addition urine Choline hydrochloride.
Comparative example 4
This example provides a kind of cement, and preparation method and formula are substantially the same manner as Example 1, the difference is that without addition 2- Chloroethyl urea ionizes bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol.
Comparative example 5
This example provides a kind of cement, and preparation method and formula are substantially the same manner as Example 1, the difference is that without addition water Mud additive.
Cement obtained by above-described embodiment 1-5 and comparative example 1-5 is tested for the property according to the method for GB175-2007, Test result is shown in Table 1.
Table 1
The data from table 1 are it is found that high-performance cement of the invention has higher compression strength and resist compared with commercial product High, the bigger corrosion resistance of intensity is rolled over, and setting time is shorter, this is the result of various composition synergistic effect.
The basic principles, main features and advantages of the present invention have been shown and described above.The technology of the industry Personnel are it should be appreciated that the present invention is not limited to the above embodiments, and what is described in the above embodiment and the description is only the present invention Principle, various changes and improvements may be made to the invention without departing from the spirit and scope of the present invention, these variation and Improvement is both fallen in the range of claimed invention.The present invention claims protection scope by appended claims and its Equivalent defines.

Claims (10)

1. a kind of high-performance cement, which is characterized in that the raw material including following parts by weight: 50-70 parts of Portland clinker, salt 5-10 parts native, 5-10 parts of agstone, 3-8 parts of attapulgite, 3-7 parts of coal dust, 5-10 parts of nanometer boron fibre, 1-5 parts of vermiculite, urine 0.3-0.8 parts of Choline hydrochloride, 2- chloroethyl urea ionize bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of ethylene glycol 0.5-1 parts, 0.5-1.5 parts of cement additive.
2. a kind of high-performance cement according to claim 1, which is characterized in that the cement additive is by following parts by weight Component be made after mixing by milling: 4,8- dioxy-dodecane -1,12- diamines and 1,3- diglycidyl ether glycerol 30-40 parts of condensation polymer, Ginsenoside F2,5- (N- biotinyl -3- aminoallyl) uridine 5'- phosplate, 4- amino-N- [3- (vinvlsulfonamido) phenyl] 25-30 parts of two lithium copolymer of naphthalimide -3,6- disulfonic acid.
3. a kind of high-performance cement according to claim 2, which is characterized in that 4, the 8- dioxy-dodecane -1,12- Diamines and 1, the preparation method of 3- diglycidyl ether glycerol condensation polymer include the following steps: 4,8- dioxy-dodecane -1, 12- diamines, 1,3- diglycidyl ether glycerol are added in dimethyl sulfoxide, 8-10 hours are stirred to react at 70-80 DEG C, back spin Dimethyl sulfoxide is evaporated off.
4. a kind of high-performance cement according to claim 3, which is characterized in that 4, the 8- dioxy-dodecane -1,12- Diamines, 1,3- diglycidyl ether glycerol, dimethyl sulfoxide mass ratio be 1:1:(3-5).
5. a kind of high-performance cement according to claim 2, which is characterized in that the Ginsenoside F2,5- (N- biotin Base -3- aminoallyl) uridine 5'- phosplate, 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- two The preparation method of two lithium copolymer of sulfonic acid includes the following steps: Ginsenoside F2,5- (N- biotinyl -3- amino allyl Base) uridine 5'- phosplate, two lithium of 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- disulfonic acid be added to In organic solvent, then initiator is added thereto, is stirred to react under nitrogen or atmosphere of inert gases 6-8 hours, back spin is evaporated off Remove organic solvent.
6. a kind of high-performance cement according to claim 5, which is characterized in that the initiator is selected from two isobutyl of azo At least one of nitrile, azobisisoheptonitrile;The organic solvent is selected from tetrahydrofuran, DMAC N,N' dimethyl acetamide, N- methyl At least one of pyrrolidones;The inert gas is selected from one of helium, neon, argon gas.
7. a kind of high-performance cement according to claim 5, which is characterized in that the Ginsenoside F2,5- (N- biotin Base -3- aminoallyl) uridine 5'- phosplate, 4- amino-N- [3- (vinvlsulfonamido) phenyl] naphthalimide -3,6- two Two lithium of sulfonic acid, organic solvent, initiator mass ratio be 2:1:0.5:(10-15): (0.01-0.03).
8. a kind of high-performance cement according to claim 1, which is characterized in that the 2- chloroethyl urea ionizes second two The preparation method of bis- (2- amino-ethyl ether) the tetraacethyl fluosilicates of alcohol, includes the following steps: 2- chloroethyl urea, ethylene glycol Bis- (2- amino-ethyl ether) tetraacethyls are added in acetone, are stirred to react at 40-60 DEG C 6-8 hours, and acetone is evaporated off in back spin, Product is added to again in the aqueous solution for the prodan that mass fraction is 10-20%, it is small to be stirred to react 10-14 at 50-60 DEG C When, water is evaporated off in back spin.
9. a kind of high-performance cement according to claim 8, which is characterized in that the 2- chloroethyl urea, ethylene glycol are double (2- amino-ethyl ether) tetraacethyl, acetone, prodan aqueous solution mass ratio be 1:1.55:(10-15): (10-20).
10. -9 described in any item a kind of high-performance cements according to claim 1, which is characterized in that the high-performance cement Preparation method includes the following steps: that by each raw material, according to parts by weight mixture, intergrinding to specific surface area is 200-300m2/ Kg obtains high-performance cement.
CN201910301251.6A 2019-04-15 2019-04-15 A kind of high-performance cement and preparation method thereof Withdrawn CN110028253A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910301251.6A CN110028253A (en) 2019-04-15 2019-04-15 A kind of high-performance cement and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910301251.6A CN110028253A (en) 2019-04-15 2019-04-15 A kind of high-performance cement and preparation method thereof

Publications (1)

Publication Number Publication Date
CN110028253A true CN110028253A (en) 2019-07-19

Family

ID=67238492

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910301251.6A Withdrawn CN110028253A (en) 2019-04-15 2019-04-15 A kind of high-performance cement and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110028253A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101602589A (en) * 2009-06-30 2009-12-16 中国地质大学(武汉) Post-tensioned prestressing pipeline vacuum grouting or mud jacking preformed material and preparation method thereof
CN103288762A (en) * 2013-05-16 2013-09-11 苏州摩尔医药有限公司 Preparation method of ketanserin intermediate 3-chloroethyl-2,4(1H,3H) quinazolinedione
CN108585562A (en) * 2018-04-24 2018-09-28 湖州知维技术服务有限公司 A kind of rapid-curing cutback cement
EP3152176B1 (en) * 2014-06-06 2020-08-05 Ascem B.v. Method for the production of a cement compound

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101602589A (en) * 2009-06-30 2009-12-16 中国地质大学(武汉) Post-tensioned prestressing pipeline vacuum grouting or mud jacking preformed material and preparation method thereof
CN103288762A (en) * 2013-05-16 2013-09-11 苏州摩尔医药有限公司 Preparation method of ketanserin intermediate 3-chloroethyl-2,4(1H,3H) quinazolinedione
EP3152176B1 (en) * 2014-06-06 2020-08-05 Ascem B.v. Method for the production of a cement compound
CN108585562A (en) * 2018-04-24 2018-09-28 湖州知维技术服务有限公司 A kind of rapid-curing cutback cement

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
耿加会等: "《商品混凝土生产与应用技术》", 30 November 2015, 中国建材工业出版社 *
魏迎春等: "《韩城区块煤层气井煤粉产出机理及主控因素研究》", 31 August 2015, 地质出版社 *

Similar Documents

Publication Publication Date Title
CN110981356A (en) Concrete taking industrial waste residues as admixture and preparation method thereof
CN111205060B (en) Industrial waste residue multi-component composite shield tunnel wall post-grouting material and preparation method thereof
CN108585925A (en) A kind of self heat-preserving concrete building block
CN110937839A (en) Synergist for recycled aggregate concrete and preparation method thereof
CN112961290A (en) Anti-mud polycarboxylic acid slump retaining water reducer and preparation method thereof
CN108975755B (en) Additive special for recycled concrete
CN111807769A (en) Slag-based highway grouting material and preparation method thereof
CN111574105A (en) Environment-friendly composite early strength water reducing agent and preparation method thereof
CN111333377A (en) High-tensile-strength concrete and preparation method thereof
CN111875405A (en) Graphite tailing foam concrete and preparation method thereof
CN114014613B (en) Salt corrosion resistant concrete and preparation method thereof
CN115368103A (en) Shrinkage-reducing anti-cracking alkali-activated slag mortar and preparation method thereof
CN114368946A (en) Mineral admixture hydraulic concrete
CN108585698B (en) Special joint filling mortar for light partition wall board
CN114591059A (en) Low-carbon internal curing lightweight concrete for 3D printing and preparation method thereof
CN109704682A (en) A kind of steel fiber reinforced concrete containing regenerative micro powder
CN110451840B (en) Composite type compacting agent
CN110577382B (en) C25 super slump retaining concrete
CN115819008B (en) High-activity low-shrinkage composite mineral admixture and preparation method thereof
CN111233394A (en) Prefabricated building reserved joint sealing dry-mixed plastering mortar and preparation method thereof
CN110028253A (en) A kind of high-performance cement and preparation method thereof
CN114149187B (en) Preparation method of modified phosphogypsum-based reinforced and toughened cementing material
CN117209222A (en) Preparation method of building 3D printing material
CN114591050A (en) High-strength cement composite material and processing method thereof
JP2019142732A (en) Hydraulic composition and concrete

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: 20190719