CN103964730B - The method of heat-conducting oil heating synthetic fluid accelerating chemicals - Google Patents

The method of heat-conducting oil heating synthetic fluid accelerating chemicals Download PDF

Info

Publication number
CN103964730B
CN103964730B CN201410168765.6A CN201410168765A CN103964730B CN 103964730 B CN103964730 B CN 103964730B CN 201410168765 A CN201410168765 A CN 201410168765A CN 103964730 B CN103964730 B CN 103964730B
Authority
CN
China
Prior art keywords
heat
conducting oil
heating
accelerating chemicals
synthetic fluid
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
CN201410168765.6A
Other languages
Chinese (zh)
Other versions
CN103964730A (en
Inventor
黄安平
赵引康
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.)
Golden Shield Garden Shanxi Building Materials Co Ltd
Original Assignee
Golden Shield Garden Shanxi Building Materials 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 Golden Shield Garden Shanxi Building Materials Co Ltd filed Critical Golden Shield Garden Shanxi Building Materials Co Ltd
Priority to CN201410168765.6A priority Critical patent/CN103964730B/en
Publication of CN103964730A publication Critical patent/CN103964730A/en
Application granted granted Critical
Publication of CN103964730B publication Critical patent/CN103964730B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

The invention discloses a kind of method of heat-conducting oil heating synthetic fluid accelerating chemicals, the method process comprises: first add the sodium polyacrylate solution of 0.1% ~ 0.5% in a kettle., again by sodium hydroxide: aluminium hydroxide 1.0 ~ 1.6 joins in reactor in molar ratio, adopt heat-conducting oil heating mode, be 120 DEG C ~ 140 DEG C in temperature of reaction, stirring velocity is under the condition of 40 ~ 80 revs/min, reacts after 1 ~ 3 hour, stopped reaction, cooling obtains the liquid accelerator of low alkali high stability.The advantage of this programme is that the method process is simple, is suitable for industrialization, save energy, pollute little, adopt heat-conducting oil heating, temperature of reaction is high, sufficient reacting, without precipitation, product stability is good, can place for a long time and not produce precipitation, adopt sodium polyacrylate solution as dielectric fluid, realize low mole prop0rtion synthetic fluid accelerating chemicals, basicity is low, PH < 10, performance is better than like product.

Description

The method of heat-conducting oil heating synthetic fluid accelerating chemicals
Technical field
The present invention relates to a kind of material of construction, more particularly, relate to a kind of synthetic method of cement concrete admixture.
Technical background
Accelerating chemicals is the admixture making cement concrete rapid coagulation, it is indispensable admixture in sprayed concrete, and the most frequently used is the liquid accelerator of aluminate class, but due to working condition and process parameter control limited, coal-fired or the steam heating mode of most employing, the aqueous solution is adopted to produce, and this mode of production to there is energy consumption high, pollute large, temperature can not control in top condition, the situation such as cause product stability bad (separate out precipitation) and time of coagulation is defective, and basicity is up to problems such as PH > 12.
Summary of the invention
The object of the present invention is to provide a kind of method of heat-conducting oil heating synthetic fluid accelerating chemicals, the method is simple to operate, pollute little, adopt heat-conducting oil heating, adopt sodium polyacrylate solution as dielectric fluid, reaction evenly, gained accelerating chemicals quality is good, stability is high, and realize low mole prop0rtion synthetic fluid accelerating chemicals, basicity is low.
For achieving the above object, the method for heat-conducting oil heating synthetic fluid accelerating chemicals in the present invention, comprises following process:
First add the sodium polyacrylate solution of solution at 0.1%-0.5% in a kettle., make the sodium polyacrylate solution in described reactor be warmed up to 60 DEG C-80 DEG C by thermal oil indirect heating;
Be that sodium hydroxide and the aluminium hydroxide of 1.0-1.6 joins in described reactor again by mol ratio, by the further indirect heating of described thermal oil, make the temperature of reaction in described reactor be 120 DEG C-140 DEG C;
While heating, utilize the agitator in described reactor to stir with the stirring velocity of 40-80 rev/min, stop after sustained reaction 1-3 hour, cooling obtains the liquid accelerator of low alkali high stability.
Described sodium polyacrylate solution is the aqueous solution.
The concentration of described aqueous sodium polyacrylate is 0.1%-0.5%.
The mol ratio of described sodium hydroxide and aluminium hydroxide is 1.0-1.6.
Described thermal oil reacts with the sodium polyacrylate in reactor described in coil pipe type of heating, sodium hydroxide, aluminium hydroxide.
Described reactor inside is provided with spiral coil pipe, described coil pipe is communicated with the heat-conducting oil heating equipment outside described reactor, and the thermal oil after heating passes into, and described coil pipe is interior to be heated the sodium polyacrylate in described reactor, sodium hydroxide, aluminium hydroxide.
In the present invention, the method for heat-conducting oil heating synthetic fluid accelerating chemicals has the following advantages: process is simple, is suitable for industrialization, save energy, pollute little, adopt heat-conducting oil heating, temperature of reaction is high, sufficient reacting, adopts sodium polyacrylate solution as dielectric fluid, without precipitation, product stability is good, can place for a long time and not produce precipitation, realize low mole prop0rtion synthetic fluid accelerating chemicals, basicity is low, PH < 10, performance is better than like product.
Accompanying drawing explanation
Fig. 1 is the process flow diagram of the method for heat-conducting oil heating synthetic fluid accelerating chemicals in the present invention.
Fig. 2 is the structural representation of coil pipe heating in the present invention.
Embodiment
Below in conjunction with accompanying drawing, the specific embodiment in the present invention is elaborated.
In the present invention, the method for heat-conducting oil heating synthetic fluid accelerating chemicals comprises the following steps:
Adding concentration (mass percentage) is in a kettle. the aqueous sodium polyacrylate of 0.1% ~ 0.5%, the mode indirect heating reactor heated with coil pipe by YD-300 mineral oil, the coil pipe passing into YD-300 mineral oil is arranged on reactor inside, as shown in Figure 2, coil pipe is arranged in the shape of a spiral, the coil pipe in reactor is entered after nearly 100 DEG C after YD-300 mineral oil is heated outside reactor, the aqueous sodium polyacrylate in reactor is made to be warmed up between 60 DEG C to 80 DEG C, by sodium hydroxide: sodium hydroxide between 1.0 ~ 1.6 of the mol ratio of aluminium hydroxide and aluminium hydroxide join in reactor, by being heated to about 200 DEG C further to the thermal oil outside reactor again, and the coil pipe passed in reactor, make temperature of reaction in reactor between 120 DEG C ~ 140 DEG C, utilize the agitator low whipping speed in reactor to be uniform stirring under the condition of 40 ~ 80 revs/min simultaneously, react after 1 ~ 3 hour, stopped reaction, cooling obtains the liquid accelerator of low alkali high stability.
Embodiment 1
The aqueous sodium polyacrylate of 0.1% of 1000kg is first joined in reactor, 70 DEG C will be warmed up in reactor by thermal oil indirect heating, add 186kg sodium hydroxide respectively again, 362kg aluminium hydroxide, continuing to be heated to temperature of reaction is 120 DEG C, low whipping speed is under the condition of 40 revs/min, uniform stirring reacts 2 hours, rear termination reaction, obtain liquid accelerator after cooling, the PH < 9 of this liquid accelerator, the volume for cement concrete is 3%, presetting period is 2-4 minute, and final setting time is 4-8 minute.
Embodiment 2
The aqueous sodium polyacrylate of 0.3% of 1000kg is first joined in reactor, 60 DEG C will be warmed up in reactor by thermal oil indirect heating, add 240kg sodium hydroxide respectively, 360kg aluminium hydroxide, continuing to be heated to temperature of reaction is 130 DEG C, and low whipping speed is under the condition of 60 revs/min, after uniform stirring reacts 1.5 hours, termination reaction, obtains liquid accelerator after cooling, the PH < 9 of this liquid accelerator.Volume for cement concrete is 2%, and the presetting period is 2-4 minute, and final setting time is 4-8 minute.
Embodiment 3
The aqueous sodium polyacrylate of 0.4% of 1000kg is first joined in reactor, be warmed up to 80 DEG C, add 174kg sodium hydroxide respectively, 226kg aluminium hydroxide is 135 DEG C in temperature of reaction, and stirring velocity is under the condition of 70 revs/min, react after 3 hours, termination reaction, obtains liquid accelerator product after cooling, PH < 10.Volume is 4%, and the presetting period is 2-4 minute, and final setting time is 4-8 minute.
Embodiment 4
The sodium polyacrylate liquid of 0.5% of 1000kg is first joined in reactor, be warmed up to 80 DEG C, add 200kg sodium hydroxide respectively, 380kg aluminium hydroxide is 140 DEG C in temperature of reaction, and stirring velocity is under the condition of 80 revs/min, react after 1 hour, termination reaction, obtains liquid accelerator product after cooling, PH < 10.Volume is 4%, and the presetting period is 2-4 minute, and final setting time is 4-8 minute.
Embodiment 5
The sodium polyacrylate liquid of 0.2% of 1000kg is first joined in reactor, be warmed up to 80 DEG C, add 150kg sodium hydroxide respectively, 340kg aluminium hydroxide is 120 DEG C in temperature of reaction, and stirring velocity is under the condition of 80 revs/min, react after 2.5 hours, termination reaction, obtains liquid accelerator product after cooling, PH < 10.Volume is 4%, and the presetting period is 2-4 minute, and final setting time is 4-8 minute.
In sum, in the present invention, the method for heat-conducting oil heating synthetic fluid accelerating chemicals is by adopting thermal oil indirect heating, there is reaction evenly, pollute little, energy consumption is low, and temperature of reaction is high, be convenient to the advantages such as temperature control, by the accurate control of temperature, the sodium aluminate generating high stability low mole prop0rtion in sodium polyacrylate solution can be ensured, obtain the accelerating chemicals that stability is high.

Claims (7)

1. a method for heat-conducting oil heating synthetic fluid accelerating chemicals, is characterized in that, comprises following process:
First add the sodium polyacrylate solution of solution at 0.1%-0.5% in a kettle., make the sodium polyacrylate solution in described reactor be warmed up to 60 DEG C-80 DEG C by thermal oil indirect heating;
Be that sodium hydroxide and the aluminium hydroxide of 1.0-1.6 joins in described reactor again by mol ratio, by the further indirect heating of described thermal oil, make the temperature of reaction in described reactor be 120 DEG C-140 DEG C;
While heating, utilize the agitator in described reactor to stir with the stirring velocity of 40-80 rev/min, stop after sustained reaction 1-3 hour, cooling obtains the liquid accelerator of low alkali high stability.
2. the method for heat-conducting oil heating synthetic fluid accelerating chemicals according to claim 1, is characterized in that, described thermal oil is mineral oil.
3. the method for heat-conducting oil heating synthetic fluid accelerating chemicals according to claim 1, is characterized in that, described sodium polyacrylate solution is the aqueous solution.
4. the method for heat-conducting oil heating synthetic fluid accelerating chemicals according to claim 2, is characterized in that, described thermal oil is YD-300 mineral oil.
5. the method for heat-conducting oil heating synthetic fluid accelerating chemicals according to claim 1, is characterized in that, described thermal oil reacts with the sodium polyacrylate in reactor described in coil pipe type of heating, sodium hydroxide, aluminium hydroxide.
6. the method for heat-conducting oil heating synthetic fluid accelerating chemicals according to claim 5, it is characterized in that, described reactor inside is provided with spiral coil pipe, described coil pipe is communicated with the heat-conducting oil heating equipment outside described reactor, and the thermal oil after heating passes into, and described coil pipe is interior to be heated the sodium polyacrylate in described reactor, sodium hydroxide, aluminium hydroxide.
7. the method for heat-conducting oil heating synthetic fluid accelerating chemicals according to claim 1, it is characterized in that, the aqueous sodium polyacrylate of 0.3% of 1000kg is first joined in described reactor, 60 DEG C will be warmed up in described reactor by described thermal oil indirect heating, add 240kg sodium hydroxide respectively, 360kg aluminium hydroxide, continuing to be heated to temperature of reaction is 130 DEG C, low whipping speed is under the condition of 60 revs/min, after uniform stirring reacts 1.5 hours, termination reaction, liquid accelerator is obtained after cooling, the PH < 9 of this liquid accelerator.
CN201410168765.6A 2014-04-25 2014-04-25 The method of heat-conducting oil heating synthetic fluid accelerating chemicals Active CN103964730B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410168765.6A CN103964730B (en) 2014-04-25 2014-04-25 The method of heat-conducting oil heating synthetic fluid accelerating chemicals

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410168765.6A CN103964730B (en) 2014-04-25 2014-04-25 The method of heat-conducting oil heating synthetic fluid accelerating chemicals

Publications (2)

Publication Number Publication Date
CN103964730A CN103964730A (en) 2014-08-06
CN103964730B true CN103964730B (en) 2016-02-03

Family

ID=51234796

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410168765.6A Active CN103964730B (en) 2014-04-25 2014-04-25 The method of heat-conducting oil heating synthetic fluid accelerating chemicals

Country Status (1)

Country Link
CN (1) CN103964730B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105906225B (en) * 2016-04-14 2017-09-15 湖北腾辰科技股份有限公司 A kind of application of discarded sewage in liquid accelerator synthesis
CN108083673A (en) * 2018-01-16 2018-05-29 山西大学 The method for having alkali liquid quick-setting agent is prepared using the tail washings for producing methacrylaldehyde

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101665336A (en) * 2009-09-23 2010-03-10 江苏博特新材料有限公司 Preparation method of low-alkaline liquid accelerating agent
CN102219433A (en) * 2011-05-04 2011-10-19 山西潞安环保能源开发股份有限公司 Low-resilience high-strength sprayed concrete liquid accelerating agent and preparation method thereof
CN102219425A (en) * 2011-04-15 2011-10-19 中铁隧道集团有限公司 Alkali-free liquid accelerating agent and preparation method thereof
CN102249592A (en) * 2011-06-01 2011-11-23 中国水利水电科学研究院 Alkali-free chlorine-free high-early-strength liquid accelerator and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101665336A (en) * 2009-09-23 2010-03-10 江苏博特新材料有限公司 Preparation method of low-alkaline liquid accelerating agent
CN102219425A (en) * 2011-04-15 2011-10-19 中铁隧道集团有限公司 Alkali-free liquid accelerating agent and preparation method thereof
CN102219433A (en) * 2011-05-04 2011-10-19 山西潞安环保能源开发股份有限公司 Low-resilience high-strength sprayed concrete liquid accelerating agent and preparation method thereof
CN102249592A (en) * 2011-06-01 2011-11-23 中国水利水电科学研究院 Alkali-free chlorine-free high-early-strength liquid accelerator and preparation method thereof

Also Published As

Publication number Publication date
CN103964730A (en) 2014-08-06

Similar Documents

Publication Publication Date Title
CN102515610B (en) Aliphatic series high efficiency water reducing agent and preparation method thereof
CN103738993B (en) A kind of carbonization reactor of energy-saving nano-calcium carbonate and preparation method
CN101704543A (en) Method for preparing cerous phosphate nano wire
CN103739563B (en) Synthesis method of imino butylated amino resin
CN103964730B (en) The method of heat-conducting oil heating synthetic fluid accelerating chemicals
CN102219423A (en) Method for preparing novel low-alkaline liquid setting accelerator
CN102367238A (en) Method for synthesizing accelerator N,N-dicyclohexyl-2-benzothiazole sulfenamide
CN105328795A (en) Gypsum slurry mixing machine
CN104628605B (en) A kind of naphthalene continuous catalysis method of sulfonating and device thereof
CN102615694A (en) Process utilizing chemical gypsum to produce high strength alpha gypsum
CN205045998U (en) Device for producing large -volumetric cement water reducing agent
CN102603680B (en) Method for preparing epoxy chloropropane by cyclizing dichloropropanol in microreactor
CN103992209A (en) Method for producing tetrabromobisphenol S
CN103523794A (en) Equipment for producing disodium octoborate tetrahydrate
CN207811695U (en) A kind of preparation system of naphthalene system slurries additive agent
CN101367553A (en) Method for synthesis of zinc molybdate or alkali type zinc molybdate
CN203212483U (en) Melting reactor for tower production of ecological loss-control humic acid compound fertilizer
CN205119904U (en) Dormancy system is with fixed attention prevented to fused salt
CN104650768A (en) Building waterproof glue and production technology thereof
CN204211652U (en) Heating-cooling device in aliphatic water reducing agent Preparation equipment
CN102659163A (en) Technological method for preparing cerium carbonate with high content of rare earth in one step
CN102745935B (en) Method for producing aliphatic high-efficiency water-reducing agent by utilizing low-content sodium sulfite pentahydrate
CN101845131A (en) Preparation method of high-efficiency water reducing agent
CN202655026U (en) Multi-layer stirring reactor
CN202936338U (en) Mixing tank device for producing high-molecular polymers

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C53 Correction of patent for invention or patent application
CI01 Correction of invention patent gazette

Correction item: Applicant

Correct: Golden Shield garden, Shanxi building materials company limited

False: The limited public affairs of Golden Shield garden, Shanxi building materials

Number: 32

Volume: 30

CI02 Correction of invention patent application

Correction item: Applicant

Correct: Golden Shield garden, Shanxi building materials company limited

False: The limited public affairs of Golden Shield garden, Shanxi building materials

Number: 32

Page: The title page

Volume: 30

ERR Gazette correction
C14 Grant of patent or utility model
GR01 Patent grant
CP03 Change of name, title or address
CP03 Change of name, title or address

Address after: 044205 Ronghe chemical industry park, Wanrong County, Yuncheng City, Shanxi Province

Patentee after: Shanxi jinwankang New Material Co., Ltd

Address before: 044205 Shanxi city of Yuncheng province Wanrong County River Building Materials Industrial Park

Patentee before: SHANXI JINDUN YUAN BUILDING MATERIALS Co.,Ltd.